CA2248237A1 - Light fixture containing optical film - Google Patents

Light fixture containing optical film Download PDF

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Publication number
CA2248237A1
CA2248237A1 CA002248237A CA2248237A CA2248237A1 CA 2248237 A1 CA2248237 A1 CA 2248237A1 CA 002248237 A CA002248237 A CA 002248237A CA 2248237 A CA2248237 A CA 2248237A CA 2248237 A1 CA2248237 A1 CA 2248237A1
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Canada
Prior art keywords
fixture
phase
light
axis
optical element
Prior art date
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Abandoned
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CA002248237A
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French (fr)
Inventor
Richard C. Allen
Timothy J. Nevitt
John A. Wheatley
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3M Co
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Minnesota Mining and Manufacturing Co
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Publication of CA2248237A1 publication Critical patent/CA2248237A1/en
Abandoned legal-status Critical Current

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Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3008Polarising elements comprising dielectric particles, e.g. birefringent crystals embedded in a matrix
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3025Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
    • G02B5/3041Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
    • G02B5/305Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3083Birefringent or phase retarding elements
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/133528Polarisers
    • G02F1/133545Dielectric stack polarisers

Abstract

An optical film is provided which comprises an antireflective layer and a disperse phase of polymeric particles disposed within a continuous birefringent matrix. The film is oriented, typically by stretching, in one or more directions. The size and shape of the disperse phase particles, the volume fraction of the disperse phase, the film thickness, and the amount of orientation are chosen to attain a desired degree of diffuse reflection and total transmission of electromagnetic radiation of a desired wavelength in the resulting film.

Description

LIGHT FIXTURE CONTAINING OPTICAL FILM

Field of the Invention sThis invention relates to optical materials which contain structures suitable for controlling optical characteristics, such as reflectance and tr~n~mission. In a further aspect, it relates to control of specific polarizations of reflected or transmitted light.

0 Background Optical films are known to the art which are conskucted from inclusions dispersed within a co~tin~ous makix. The characteristics of these inclusions canbe manipulated to provide a range of reflective and tr~n~mi~ive properties to the film. These characteristics include inclusion size with respect to wavelength 5 within the film, inclusion shape and alignmPnt inclusion volumekic fill factor and the degree of refractive index mi~m~tçh with the continuous makix along the film's three orthogonal axes.
Conventional absorbing (dichroic) polarizers have, as their inclusion phase, inorganic rod-like chains of light-absorbing iodine which are aligned within a 20 polymer matrix. Such a film will tend to absorb light polarized with its electric field vector ~lignP~l parallel to the rod-like iodine chains, and to kansmit light polarized perpendicular to the rods. Because the iodine chains have two or more ~lim~n~ions that are small colllpaled to the wavelength of visible light, and because the number of chains per cubic wavelength of light is large, the optical l~iop~. lies 2s of such a film are predominately specular, with very little diffuse k~n~mi~ion through the film or diffuse reflection from the film surfaces. Like most other commercially available polarizers, these polarizing films are based on polarization-selective absorption.
Films filled with inorganic inclusions with dirr~,lclll characteristics can 30 provide other optical tr~n~mi~sion and reflective pl~t:.lies. For example, coated mica flakes with two or more ~lim~n~ ns that are large colll~ ed with visible W O 97/3222S PCTrUS97/02995 wavelengths, have been incorporated into polymeric films and into paints to impart a metallic glitter. These flakes can be manipulated to lie in the plane of the film, thereby in~alLillg a strong directional depe~ nce to the reflective appearance.
Such an effect can be used to produce security screens that are highly reflective for 5 certain viewing angles, and tr~n~mi~ive for other viewing angles. Large flakeshaving a coloration (specularly selective reflection) that depends on alignment with respect to incident light, can be incorporated into a film to provide evidence of p~l;ng. In this application, it is n~cees~ry that all the flakes in the film be similarly aligned with respect to each other.
However, optical films made from polymers filled with inorganic inclusions suffer from a variety of inr~ ies. Typically, adhesion between the inorganic particles and the polymer matrix is poor. Consequently, the optical olJel lies of the film decline when stress or strain is applied across the matrix, both because the bond between the matrix and the inclusions is colllplu.~ e-l and 15 because the rigid inorganic inclusions may be fractured. Furthermore, ~lignment of inorganic inclusions requires process steps and considerations that complicate m~nl-f~ct~ring.
Other films, such as that disclosed in U.S. 4,688,900 (Doane et. al.), consists of a clear light-transmitting continuous polymer matrix, with droplets of 20 light mo~ ting liquid crystals dispersed within. Stretching of the material reportedly results in a distortion of the liquid crystal droplet from a spherical to an ellipsoidal shape, with the long axis of the ellipsoid parallel to the direction of stretch. U.S. 5,301,041 (Konuma et al.) make a similar disclosure, but achieve the distortion of the liquid crystal droplet through the application of ples~ule. A.2s Aphonin, "Optical Plul)c~Lies of Stretched Polymer Dispersed Liquid Crystal Films: Angle-Dependent Polarized Light Scattering, Liquid Crvstals. Vol. 19, No.4, 469-480 (1995), discusses the optical plOpC~ Lies of stretched films con~i.cting of liquid crystal droplets disposed within a polymer matrix. He reports that the elongation of the droplets into an ellipsoidal shape, with their long axes parallel to 30 the stretch direction, imparts an oriented l)il~irfingence (refractive index differenc among the ~iimen~ional axes of the droplet) to the droplets, resulting in a relative refractive index mi~m~tch between the dispersed and continuous phases along certain film axes, and a relative index match along the other film axes. Such liquid crystal droplets are not small as compared to visible wavelengths in the film, and thus the optical properties of such films have a substantial diffuse component to their reflective and tr~n~mi~ive plupclLies. Aphonin suggests the use of these m~teri~l~ as a polarizing diffuser for backlit twisted nematic LCDs. However, optical films employing liquid crystals as the disperse phase are ~ub~ lly limited in the degree of refractive index mi~m~trh between the matrix phase and the dispersed phase. Furthermore, the birefringence of the liquid crystal o component of such films is typically sensitive to telllp~ldlul~.
U. S. 5,268,225 (Isayev) discloses a composite ~ t~ made from thermotropic liquid crystal polymer blends. The blend consists of two liquid crystal polymers which are immiscible with each other. The blends may be cast into a film concicting of a dispersed inclusion phase and a continuous phase. When the film is stretched, the dispersed phdse forms a series of fibers whose axes are aligned in the direction of stretch. While the film is described as having improved mechanical properties, no mention is made ofthe optical plo~lLies ofthe film.
However, due to their liquid crystal nature, films of this type would suffer from the infirmities of other liquid crystal materials discussed above.
Still other films have been made to exhibit desirable optical pr~ ~ Lies through the application of electric or m~n~tic fields. For exarnple, U. S.
5,008,807 (Waters et al.) describes a liquid crystal device which consists of a layer of fibers perme~ted with liquid crystal m~t~ri~l and disposed between two electrodes. A voltage across the electrodes produces an electric field~ which 2s changes the birt;fiingent l,lopellies of the liquid crystal material, resulting in various degrees of mi~m~tçll between the refractive indices of the fibers and the liquid crystal. However, the requirement of an electric or magnetic field is inconvenient and undesirable in many applications, particularly those where existing fields might produce i~ lr~.ence.
Other optical films have been made by incorporating a dispersion of inclusions of a first polymer into a second polymer, and then stretching the resulting composite in one or two directions. U. S. 4,871,784 (Otonari et al. ) is exemplative of this technology. The polymers are selected such that there is lowadhesion between the dispersed phase and the surrounding matrix polymer, so thatan elliptical void is formed around each inclusion when the film is stretched. Such voids have ~lim~ncions of the order of visible wavelengths. The refractive indexmi.~m~tçh between the void and the polymer in these "microvoided" films is typically quite large (about 0.5), c~-lcing substantial diffuse reflection. However, the optical ~lo~ lies of microvoided m~t~ l c are difficult to control because of variations of the geometry of the interfaces, and it is not possible to produce a film 0 axis for which refractive indices are relatively m~t~hetl as would be useful for polarization-sensitive optical propt;l lies. Furthermore, the voids in such material can be easily collapsed through exposure to heat and pressure.
Optical films have also been made wherein a dispersed phase is det~nninictically arranged in an ordered pattern within a continuous matrix. U. S.
5,217,794 (Schrenk) is exemplative ofthis technology. There, a lamellar polymeric film is disclosed which is made of polymeric inclusions which are large compared with wavelength on two axes, disposed within a continuous matrix of another polymeric material. The refractive index of the dispersed phase differs significantly from that of the continuous phase along one or more of the l~min~1e's axes, and is relatively well m~tehe~l along another. Because of the ordering of the dispersed phase, films of this type exhibit strong iridescence (i.e., illle,r~,~,.,ce-based angle dependent coloring) for in.ct~ncec in which they are substantially reflective. As a result, such films have seen limited use for optical applications where optical diffusion is desirable.
2s There thus remains a need in the art for an optical material coneieting of a continuous and a dispersed phase, wherein the refractive index mi.em~tch betweenthe two phases along the material's three ~limen.eional axes can be conveniently and perm~n~ntly manipulated to achieve desirable degrees of diffuse and specular reflection and tr~nemi~eion, wherein the optical material is stable with respect to 30 stress, strain, te~ ld~ dirrt,~nces, and electric and m~gn~tic fields, and wherein the optical material has an in~ignificant level of iri~escçnce. These and other needs are met by the present invention, as hereinafter disclosed.

Brief Description of the Drawings s FIG. I is a sr.ll~om~tic drawing illustrating an optical body made in accoldance with the present invention, wherein the disperse phase is arranged as a series of elong~tecl masses having an ess~nti~lly circular cross-section;
FIG. 2 is a s~.h~m~tic drawing illu~ g an optical body made in accordance with the present invention, wherein the disperse phase is arranged as a o series of elongated masses having an ess~nti~lly elliptical cross-section;
FIGS. 3a-e are s~h~m~tic drawings illu~lldLillg various shapes of the disperse phase in an optical body made in accordance with the present invention;FIG. 4a is a graph of the bidirectional scatter distribution as a function of scattered angle for an oriented film in accordance with the present invention for s light polarized perpendicular to orientation direction;
FIG. 4b is a graph of the bidirectional scatter distribution as a function of scattered angle for an oriented film in accordance with the present invention for light polarized parallel to orientation direction;
FIG. 5 is a schPm~tic represçnt~tion of a multilayer film made in accordance with the present invention;
FIGS. 6a and 6b are electron micrographs of optical films made in accordance with the present invention;
FIG. 7 is a perpendicular tr~n~mi~sion spectrum for films made in accordance with the present invention;
2s FIG. 8 is a sch~-m~tic diagrarn illustrating the use of the films of the present invention as high efficiency light extractors for optical fibers; and FIGS. 9A and 9B are graphs showing relative gain as a function of angle for the films of the present invention and for a commercially available optical film, respectively.

W O 97/32225 PCTAUS97tO2995 Sum mary oftheInvention In one aspect, the present invention relates to a diffusely reflective film or other optical body comprising a birefringent continuous polymeric phase and a substantially nonbirefringent disperse phase disposed within the continuous phase.
s The indices of refraction of the continuous and disperse phases are subst~nti~lly mi~m~tched (i.e., differ from one another by more than about 0.05) along a first of three mutually orthogonal axes, and are substantially matched (i.e., differ by less than about 0.05) along a second of three mutually orthogonal axes. In some embo.liment~, the indices of refraction of the continuous and disperse phases can lo be substantially m~t~he~l or micm~trhed along, or parallel to, a third of three m~ lly orthogonal axes to produce a mirror or a polarizer. Incident light polarized along, or parallel to, a mi~m~tçhed axis is sc~lL.,lcd, resulting in significant diffuse reflection. Incident light polarized along a m~tçhed axis isscattered to a much lesser degree and is significantly spectrally l~ans~ ed. These s properties can be used to make optical films for a variety of uses, including low loss (significantly nonabsorbing) reflective polarizers for which polarizations of light that are not significantly transmitted are diffusely reflected.
In a related aspect, the present invention re}ates to an optical film or other optical body comprising a bherlh~gent continuous phase and a disperse phase, 20 wherein the indices of refraction of the continuous and disperse phases are substantially m~tc.h~d (i.e., wherein the index difference between the continuous and disperse phases is less than about 0.05) along an axis perpendicular to a surface of the optical body.
In another aspect, the present invention relates to a composite optical body 25 comprising a polymeric continuous birefringent first phase in which the disperse second phase may be birefringent, but in which the degree of match and mi~m~t~h in at least two orthogonal directions is primarily due to the birefringence of the first phase.
In still another aspect, the present invention relates to a method for 30 obtaining a diffuse reflective polarizer, comprising the steps of: providing a first resin, whose degree of birefringence can be altered by application of a force field, W O 97/32225 PCT~US97/02995 as through ~li,n~ ional orientation or an applied electric field, such that the resulting resin m~teri~l has, for at least two orthogonal directions, an index of refraction dirre~lce of more than about 0.05; providing a second resin, dispersed within the first resin; and applying said force field to the composite of both resins 5 such that the indices of the two resins are approximately m~tehe~l to within less than about 0.05 in one of two directions, and the index difference between first and second resins in the other of two directions is greater than about 0.05. In a related embo~limPnt, the second resin is dispersed in the first resin after imposition of the force field and subsequent alteration of the birefringen~-e of the first resin.
lo In yet another aspect, the present invention relates to an optical body acting as a reflective polarizer with a high extinction ratio. In this aspect, the index difference in the match direction is chosen as small as possible and the dirrelel.ce in the mi~m~t~h direction is m~ximi7~ The volume fraction, thickness, and disperse phase particle size and shape can be chosen to maximize the extinction 15 ratio, although the relative importance of optical tr~n~mi~sion and reflection for the different polarizations may vary for dirr~e.ll applications.
In another aspect, the present invention relates to an optical body comprising a continuous phase, a disperse phase whose index of refraction differs t'rom said continuous phase by greater than about 0.05 along a first axis and by less 20 than about 0.05 along a second axis orthogonal to said first axis, and a dichroic dye. The optical body is preferably oriented along at least one axis. The dichroic dye improves the extinction coefficient of the optical body by absorbing, in addition to scattering, light polarized parallel to the axis of orientation.
In another aspect of the present invention, an optical body is provided 25 which has at least first and second phases that are co-continuous along at least one axis. The index of refraction of the first phase differs from that of the second phase by greater than about 0.05 along a first axis and by less than about 0.05 along a second axis orthogonal to said first axis. In other embo-liment~, three or more co-continuous phases may be used to achieve the same or similar m~trhes and 30 miim~tclles along ml~hl~lly perpendicular axes.

In still another aspect of the present invention, an optical body is provided which comprises a film having a continuous and disperse phase, with an antireflective layer disposed thereon. Such films exhibit a flat tr~n~mi~ion curve as a function of the wavelength of light, which tends to minimi7e any changes in5 color to a resultant display device into which the reflective polarizer is incorporated.
In the various aspects of the present invention, the reflection and tr~nsmi~ion properties for at least two orthogonal polarizations of in~ nt lightare clet~nin-o~ by the selection or manipulation of various parameters, including 10 the optical indices of the continuous and disperse phases, the size and shape of the disperse phase particles, the volume fraction of the disperse phase, the thickness of the optical body through which some fraction of the incident light is to pass, and the wavelength or wavelength band of electrom~gn~tic radiation of interest.
The magnitude of the index match or mi~m~t~h along a particular axis will 15 directly affect the degree of sc~ hlg of light polarized along that axis. In general, scattering power varies as the square of the index mi~m~t~h Thus, the larger theindex mi~m~t~l along a particular axis, the stronger the scattering of light polarized along that axis. Co~ ely, when the mism~tch along a particular axis is small, light polarized along that axis is scattered to a lesser extent and is thereby 20 transmitted specularly through the volume of the body.
The size of the disperse phase also can have a significant effect on sC~ttpring If the disperse phase particles are too small (i.e., less than about 1/30 the wavelength of light in the medium of interest) and if there are many particles per cubic wavelength, the optical body behaves as a medium with an effective 2s index of refraction somewhat between the indices of the two phases along any given axis. In such a case, very little light is scattered. If the particles are too large, the light is specularly reflecterl from the particle surface, with very little diffusion into other directions. When the particles are too large in at least two orthogonal directions, undesirable iridescence effects can also occur. Practical30 limits may also be reached when particles becolllc large in that the thickness of the optical body becomes greater and desirable mechanical plop~,llies are complo"lised.
The shape of the particles of the disperse phase can also have an effect on the sc~ttering of light. The depolarization factors of the particles for the electric field in the index of refraction match and mi~m~tçh directions can reduce or enhance the amount of scattering in a given direction. The effect can either add or detract from the amount of scalL~l;ng from the index mism~trh, but generally has a small influence on scattering in the p,~re"ed range of plOp~,. lies in the present invention.
o The shape of the particles can also influence the degree of diffusion of light scattered from the particles. This shape effect is generally small but increases as the aspect ratio of the geometrical cross-section of the particle in the plane perpendicular to the direction of incidence of the light increases and as the particles get relatively larger. In general, in the operation of this invention, the disperse phase particles should be sized less than several wavelengths of light in one or two mutually orthogonal ~limen~;ons if diffuse, rather than specular, reflection is preferred.
Dim~n~ional ~lignm~nt is also found to have an effect on the scattering behavior of the disperse phase. In particular, it has been observed, in optical bodies made in accordance with the present invention, that aligned sc~L~elel~ will not scatter light symmetrically about the directions of spec~ r tr~n~mi~ion or reflection as randomly aligned scatterers would. In particular, inclusions that have been elongated by orientation to resemble rods scatter light primarily along (ornear) a cone centered on the orientation direction and having an edge along the specularly transmitted direction. For example, for light incident on such an elongated rod in a direction perpendicular to the orientation direction, the scattered light appears as a band of light in the plane perpendicular to the orientation direction with an intensity that decreases with increasing angle away from the spec~ r directions. By tailoring the geometry of the inclusions, some control over the distribution of scattered light can be achieved both in the tr~n~mi~ive h~mi~ph~re and in the reflective hPmi~phPre.

W O 97/3222S PCTrUS97/02995 The volume fraction of the disperse phase also affects the sc~ g of light in the optical bodies of the present invention. Within certain limits, increasing the volume fraction of the disperse phase tends to increase the amount of scatteringthat a light ray experiences after entering the body for both the match and s mi~m~tch directions of polarized light. This factor is hnpoll~l~ for controlling the reflection and tr~nemieeion l,ropcl lies for a given application. However, if the volume fraction of the disperse phase becomes too large, light scattering rlimini.ehPs Without wishing to be bound by theory, this appears to be due to the fact that the disperse phase particles are closer together, in terms of the wavelength o of light, so that the particles tend to act together as a smaller number of large effective particles.
The thickness of the optical body is also an hlll,ol l~ll control parameter which can be manipulated to affect reflection and tr~nemiesion l)r~pcllies in the present invention. As the thickness of the optical body increases, diffuse reflection s also increases, and tr~nemie~eion, both spec~ r and diffuse, decreases.
While the present invention will often be described herein with reference to the visible region of the spectrum, various embodiments of the present inventioncan be used to operate at di~lent wavelengths (and thus frequencies) of electromagnetic radiation through a~ropl;ate scaling ofthe components ofthe 20 optical body. Thus, as the wavelength increases, the linear size of the components of the optical body are increased so that the ~iimloneions, measured in units ofwavelength, remain ~ lately constant. Another major effect of ch~nging wavelength is that, for most materials of interest, the index of refraction and the absorption coefficient change. However, the principles of index match and 25 miem~t~ h still apply at each wavelength of interest.

Detailed D~s~ ;~,lion of the Invention Introduction As used herein, the terms "specular reflection" and "specular reflectance"
30 refer to the reflectance of light rays into an emergent cone with a vertex angle of 16 degrees centered around the specular angle. The terms "diffuse reflection" or W O 97/32225 PCTnUS97/02995 "diffuse reflectance" refer to the reflection of rays that are outside the specular cone defined above. The terms "total reflectance" or "total reflection" refer to the combined reflect~n~e of all light from a surface. Thus, total reflection is the sum of specular and diffuse reflection.
Similarly, the terms "specular tr~nemieeion" and '~spec~ r transmittance"
are used herein in reference to the tr~nemieeion of rays into an emergent cone with a vertex angle of 16 degrees centered around the specular direction. The terms "diffuse tr~nemieslon" and "diffuse lld.ls~ ce" are used herein in reference to the tr~nemiesion of all rays that are outside the specular cone defined above. The 0 terms "total tr~nemiesion~ or "total l~a~ ce" refer to the combined tr~nemieeion of all light through an optical body. Thus, total tr~nemieeion is the sum of specular and diffuse tr~nemi~eion.
As used herein, the term "extinction ratio" is defined to mean the ratio of total light transmitted in one polarization to the light transmitted in an orthogonal s polarization.
FIGS. 1-2 illustrate a first embodiment of the present invention. In accordance with the invention, a diffusely reflective optical film 10 or other optical body is produced which consists of a birefringent matrix or continuous phase 12 and a discontinuous or disperse phase 14. The birefringence of the continuous phase is typically at least about 0.05, preferably at least about 0.1, more preferably at least about 0.15, and most preferably at least about 0.2.
The indices of refraction of the continuous and disperse phases are subst~nti~lly m~tçhe-l (i.e., differ by less than about 0.05) along a first of three mlltll~lly orthogonal axes, and are subst~nti~lly miem~tçhecl (i.e., differ by more than about 0.05) along a second of three mntll~l Iy orthogonal axes. Preferably, the indices of refraction of the continuous and disperse phases differ by less than about 0.03 in the match direction, more preferably, less than about 0.02, and most preferably, less than about 0.01. The indices of refraction of the continuous and disperse phases preferably differ in the miem~tch direction by at least about 0.07, more preferably, by at least about 0.1, and most preferably, by at least about 0.2.

W O 97/32225 PCTrUS97/02995 The mi~m~t~h in refractive indices along a particular axis has the effect that incident light polarized along that axis will be substantially scattered, resulting in a significant amount of reflection. By contrast, incident light polarized along an axis in which the refractive indices are m~tc.h~d will be spectrally transmitted or 5 reflected with a much lesser degree of sc~lt~ g. This effect can be utilized to make a variety of optical devices, including reflective polarizers and mirrors.
The present invention provides a practical and simple optical body and method for m~king a reflective polarizer, and also provides a means of obtaining a continuous range of optical ~o~; c~ Lies according to the principles described herein.
0 Also, very efficient low loss polarizers can be obtained with high extinction ratios.
Other advantages are a wide range of practical materials for the disperse phase and the continuous phase, and a high degree of control in providing optical bodies of consistent and predictable high quality p~lro....~ çe.

15 Effect of Index Match~ m~trl In the preferred embodiment, the materials of at least one of the continuous and disperse phases are of a type that undergoes a change in refractive index upon orientation. Consequently, as the film is oriented in one or more directions, refractive index m~tt~h~s or mi.cm~tçh~os are produced along one or more axes. By 20 careful manipulation of orientation parameters and other processing conditions, the positive or negative birefringence of the matrix can be used to induce diffuse reflection or tr~n.cmi~sion of one or both polarizations of light along a given axis.
The relative ratio between tr~n~mi.~sion and diffuse reflection is dependent on the concentration of the disperse phase inclusions, the thickness of the film, the square 25 of the difference in the index of refraction between the continuous and disperse phases, the size and geometry of the disperse phase inclusions, and the wavelength or wavelength band of the incid~nt r~ tion The magnitude of the index match or mi~m~tçh along a particular axis directly affects the degree of scaLI~fillg of light polarized along that axis. In 30 general, sc~lle~ g power varies as the square of the index mi.~m~t~h Thus, the larger the index mi~m~tch along a particular axis, the stronger the sC~tt~ring of light polarized along that axis. Conversely, when the mi~m~trh along a particular axis is small, light polarized along that axis is scattered to a lesser extent and is thereby transmitted specularly through the volume of the body.
FIGS. 4a-b demonstrate this effect in oriented films made in accordance s with the present invention. There, a typical Bidirectional Scatter Distribution Function (BSDF) measurement is shown for normally incident light at 632.8 nm.
The BSDF is described in J. Stover, "Optical Scattering Measurement and Analysis" (1990). The BSDF is shown as a function of sca~ ,d angle for polarizations of light both perpendicular and parallel to the axis of Gl;~n~ion. A
o scattered angle of zero co,lesyonds to ~m~c~ttered (spectrally transmitted) light.
For light polarized in the index match direction (that is, perpendicular to the orientation direction) as in FIG. 4a, there is a significant specularly tr~n~mitted peak with a sizable colllyollent of diffusely transmitted light (scattering angle between 8 and 80 degrees), and a small component of diffusely reflected light 15 (scattering angle larger than 100 degrees). For light polarized in the index mi~m~tçh direction (that is, parallel to the orientation direction) as in FIG. 4b, there is negligible specularly tl~lslllilled light and a greatly reduced component of diffusely lldl~slllilled light, and a sizable diffusely reflected component. It should be noted that the plane of scattering shown by these graphs is the plane 20 perpendicular to the orientation direction where most of the sc~Ueled light exists for these elongated inclusions. Scattered light contributions outside of this plane are greatly red~.ce-l If the index of refraction of the inclusions (i.e., the disperse phase) m~tçhes that of the continuous host media along some axis, then incident light polarized2s with electric fields parallel to this axis will pass through ~ cnllel~d regardless of the size, shape, and density of inclusions. If the indices are not m~tched alongsome axis, then the inclusions will scatter light polarized along this axis. Forscall.,~ of a given cross-sectional area with dimensions larger than apyl~xhllately ~/30 ( where ~ is the wavelength of light in the media), the strength 30 of the scalL~,.;llg is largely determin~d by the index mi~m~tçh The exact size, shape and ~lignm~nt of a mi~m~tch~d inclusion play a role in ~letermining how W O 9713222S PCT~US97/02995 much light will be scattered into various directions from that inclusion. If thedensity and thickness of the scattering layer is sufficient, according to multiple scattering theory, incident light will be either reflected or absorbed, but not L~d, regardless of the details of the scatterer size and shape.
s When the material is to be used as a polarizer, it is preferably processed, as by stretching and allowing some ~lim~n.eional relaxation in the cross stretch in-plane direction, so that the index of refraction dirrelcnce between the continuous and disperse phases is large along a first axis in a plane parallel to a surface of the material and small along the other two orthogonal axes. This results in a large o optical anisotropy for electromagnetic radiation of dirr~lcnt polarizations.
~ome of the polarizers within the scope of the present invention are elliptical polarizers. In general, elliptical polarizers will have a di~.lcc in index of refraction between the disperse phase and the continuous phase for both the stretch and cross-stretch directions. The ratio of forward to back scattering is1S dependent on the dirr~lellce in refractive index between the disperse and continuous phases, the concentration of the disperse phase, the size and shape of the disperse phase, and the overall thickness of the film. In general, elliptical diffusers have a relatively small difference in index of refraction between the particles of the disperse and continuous phases. By using a birefringent polymer-based diffuser, highly elliptical polarization sensitivity (i.e., diffuse reflectivity depending on the polarization of light) can be achieved. At an extreme, where the index of refraction of the polymers match on one axis, the elliptical polarizer will be a diffuse reflecting polarizer.

2s Methods of Obtaining Index Match/Mismatch The ~n~teri~l~ selected for use in a polarizer in accordance with the present invention, and the degree of orientation of these materials, are preferably chosen so that the phases in the fini~h~(l polarizer have at least one axis for which the associated indices of refraction are subst~nti~lly equal. The match of refractive indices associated with that axis, which typically, but not necess~rily, is an axis transverse to the direction of orientation, results in substantially no reflection of light in that plane of polarization.
The disperse phase may also exhibit a decrease in the refractive index associated with the direction of orientation after ~LIetcl~ g. If the birefringence of 5 the host is positive, a negative strain in~ cec~ birefringence of the disperse phase has the advantage of increasing the difference between indices of refraction of the adjoining phases associated with the orientation axis while the reflection of light with its plane of polarization perpendicular to the orientation direction is still negligihle. Differences between the indices of refraction of adjoining phases in the o direction orthogonal to the orientation direction should be less than about 0.05 after orientation, and preferably, less than about 0.02.
The ~1icperse phase may also exhibit a positive strain ind~-ced birefringence.
However, this can be altered by means of heat tre~tment to match the lcL~;tive index of the axis perpendicular to the orientation direction of the continuous phase.
5 The temperature of the heat tre~tm~nt should not be so high as to relax the birefringence in the continuous phase.

Size of Di.,~el ~e Phase The size of the disperse phase also can have a significant effect on 20 scattering. If the disperse phase particles are too small (i.e., less than about 1/30 the wavelength of light in the medium of interest) and if there are many particles per cubic wavelength, the optical body behaves as a medium with an effective index of refraction somewhat between the indices of the two phases along any given axis. In such a case, very little light is scattered. If the particles are too 25 large, the light is specularly reflected from the surface of the particle, with very little diffusion into other directions. When the particles are too large in at least two orthogonal direction~ undesirable iridescence effects can also occur. Practical limits may also be reached when particles become large in that the thickness of the optical body becomes greater and desirable mech~nical properties are 30 collll)romised.

W O 97132225 PCTrUS97102995 The ~ n~ ions of the particles of the disperse phase after ~lignmçnt can vary depending on the desired use of the optical m~tçri~l. Thus, for example, the dimensions of the particles may vary depending on the wavelength of electromagnetic radiation that is of interest in a particular application, with different ~limen.~ions required for reflecting or h~s.~ g visible, ultraviolet, infrared, and microwave radiation. Generally, however, the length of the particles should be such that they are approximately greater than the wavelength of electromagnetic radiation of interest in the medium, divided by 30.
Preferably, in applications where the optical body is to be used as a low o loss reflective polarizer, the particles will have a length that is greater than about 2 times the wavelength of the electrom~gn.otic radiation over the wavelength range of interest, and preferably over 4 times the wavelength. The average diameter of the particles is preferably equal or less than the wavelength of the electrom~gn~ticradiation over the wavelength range of interest, and preferably less than 0.5 of the desired wavelength. While the ~limen~ions of the disperse phase are a secondary consideration in most applications, they become of greater importance in thin film applications, where there is comparatively little diffuse reflection.

Geometly of D;i.~,el ie Phase While the index mi~m~tçh is the predominant factor relied upon to promote scattering in the films of the present invention (i.e., a diffuse mirror or polarizer made in accordance with the present invention has a substantial mi~m~tch in the indices of refraction of the continuous and disperse phases along at least one axis), the geometry of the particles of the disperse phase can have a secondary effect on scattering. Thus, the depolarization factors of the particles for the electric field in the index of refraction match and mi~m~tch directions can reduce or enh~nce the amount of sc~ g in a given direction. For exarnple, when the disperse phase is elliptical in a cross-section taken along a plane perpendicular to the axis of orientation, the elliptical cross-sectional shape of the disperse phase contributes to the asymmetric diffusion in both back scattered light and forward scattered light.
The effect can either add or detract from the amount of scattering from the index WO 97132225 PCT/US97tO2995 mi~m~tçh, but generally has a small influence on sca~ g in the prerel.~;d range of prope,lies in the present invention.
The shape of the disperse phase particles can also influence the degree of diffusion of light scattered from the particles. This shape effect is generally small s but increases as the aspect ratio of the geometrical cross-section of the particle in the plane perpendicular to the direction of incidence of the light increases and as the particles get relatively larger. In general, in the operation of this invention, the disperse phase particles should be sized less than several wavelengths of light in one or two mutually orthogonal (lim~on~ions if diffuse, rather than specular, 0 reflection is plefe,l. d.
Preferably, for a low loss reflective polarizer, the preferred embodiment consists of a disperse phase disposed within the continuous phase as a series ofrod-like structures which, as a consequence of orientation, have a high aspect ratio which can enh~nce reflection for polarizations parallel to the orientation direction l s by increasing the scattering strength and dispersion for that polarization relative to polarizations perpendicular to the orientation direction. However, as indicated in FIGS. 3a-e, the disperse phase may be provided with many dirr~;~ent geometries.
Thus, the disperse phase may be disk-shaped or elongated disk-shaped, as in FIGS.
3a-c, rod-shaped, as in FIG. 3d-e, or spherical. Other embodiments are contemplated wherein the disperse phase has cross sections which are approxim~tely elliptical (including circular), polygonal, irregular, or a combination of one or more of these shapes. The cross-sectional shape and size of the particles of the disperse phase may also vary from one particle to another, or from one region of the film to another (i.e., from the surface to the core).
2s In some embo-liment~, the disperse phase may have a core and shell construction, wherein the core and shell are made out of the same or different m~teri~l~, or wherein the core is hollow. Thus, for example, the disperse phase may consist of hollow fibers of equal or random lengths, and of ul~rO~ or non-uniform cross section. The interior space of the fibers may be empty, or may be occupied by a suitable medium which may be a solid, liquid, or gas, and may be organic or inorganic. The refractive index of the medium may be chosen in W O 97/32225 PCTrUS97/02995 consideration of the refractive indices of the disperse phase and the continuousphase so as to achieve a desired optical effect (i.e., reflection or polarization along a given axis).
The geometry of the disperse phase may be arrived at through suitable orientation or processing of the optical material, through the use of particles having a particular geometry, or through a combination of the two. Thus, for example, adisperse phase having a subst~nti~lly rod-like structure can be produced by orienting a film con~ ting of a~pro~i,l,ately spherical disperse phase particlesalong a single axis. The rod-like structures can be given an elliptical cross-section o by orienting the film in a second direction perpendicular to the first. As a further example, a disperse phase having a substantially rod-like structure in which therods are rectangular in cross-section can be produced by orienting in a single direction a film having a ~ perse phase consisting of a series of essenti~lly rectangular flakes.
Stretching is one convenient manner for arriving at a desired geometry, since stretching can also be used to induce a dirrelence in indices of refraction within the material. As indicated above, the orientation of films in accordance with the invention may be in more than one direction, and may be sequential or simultaneous.
In another example, the components of the continuous and disperse phases may be extruded such that the disperse phase is rod-like in one axis in the unoriented film. Rods with a high aspect ratio may be generated by orienting in the direction of the major axis of the rods in the extruded film. Plate-like structures may be generated by orienting in an orthogonal direction to the major axis of the rods in the extruded film.
The structure in FIG. 2 can be produced by asymmetric biaxial orientation of a blend of essentially spherical particles within a continuous matrix.
Alternatively, the structure may be obtained by incorporating a plurality of fibrous structures into the matrix m~t~ri~ ligning the structures along a single axis, and orienting the mixture in a direction transverse to that axis. Still another method for obtaining this structure is by controlling the relative viscosities, shear, or surface W O 97132225 PCTrUS97/02995 tension of the components of a polymer blend so as to give rise to a fibrous disperse phase when the blend is extruded into a film. In general, it is found that the best results are obtained when the shear is applied in the direction of extrusion.

s Dimensional Alignment of Disperse Phase Dimensional ~ nment is also found to have an effect on the scattering behavior of the disperse phase. In particular, it has been observed in optical bodies made in accordallce with the present invention that aligned scatterers will not scatter light symmetrically about the directions of specular tr~ncmi~ion or o reflection as randomly aligned SCall~.le.~i would. In particular, inclusions that have been elongated through orientation to resemble rods scatter light primarily along (or near) the surface of a cone centered on the orientation direction and along the specularly transmitted direction. This may result in an anisotropic distribution of scattered light about the specular reflection and specular tr~n~mi~ion directions.
For example, for light incident on such an elongated rod in a direction perpendicular to the orientation direction, the scattered light appears as a band of light in the plane perpendicular to the orientation direction with an intensity that decreases with increasing angle away from the specular directions. By tailoring the geometry of the inclusions, some control over the distribution of scattered light can 20 be achieved both in the tr~n~mi~ive hemisphere and in the reflective hemisphere.

Dimensions of Di~ ~ ;,e Phase In applications where the optical body is to be used as a low loss reflective polarizer, the structures of the disperse phase preferably have a high aspect ratio, 25 i.e., the structures are substantially larger in one tlim~n~ion than in any other ~1imPn~ion. The aspect ratio is preferably at least 2, and more preferably at least 5.
The largest ~1imen~ion (i.e., the length) is preferably at least 2 times the wavelength of the electrom~gnetic radiation over the wavelength range of interest, and more~le~lably at least 4 times the desired wavelength. On the other hand, the smaller 30 (i.e., cross-sectional) ~iim~n.~jons of the structures of the disperse phase are _19_ W O 97/32225 PCTrUS97/02995 preferably less than or equal to the wavelength of interest, and more p~er~ably less than 0.5 times the wavelength of interest.

Volume Fraction of Disperse Phase The volume fraction of the disperse phase also affects the scattering of light in the optical bodies of the present invention. Within certain limits, increasing the volume fraction of the disperse phase tends to increase the amount of scatteringthat a light ray experiences after enterin~ the body for both the match and mi~m~tch directions of polarized light. This factor is important for controlling the reflection and tr~ncmi~ion properties for a given application.
The desired volume fraction of the disperse phase will depend on many factors, including the specific choice of materials for the continuous and disperse phase. However, the volume fraction of the disperse phase will typically be at least about 1% by volume relative to the continuous phase, more preferably within the s range of about 5 to about 15%, and most preferably within the range of about 15 to about 30%.

Co-Continuous Phases When the volume fraction for binary blends of high polymers of roughly equivalent viscosity approaches 50%, the distinction between the disperse and continuous phases becomes difficult, as each phase becomes continuous in space.
Depending upon the materials of choice, there may also be regions where the first phase ~l.pe~s to be dispersed within the second, and vice versa. For a description of a variety of co-continuous morphologies and for methods of evaluating, analyzing, and characterizing them, see Sperling and the references cited therein (L.H. Sperling, "Microphase Structure", Encyclopedia of Polymer Science and En~ineerin~, 2nd Ed., Vol. 9, 760-788, and L.H. Sperling, Chapter 1 "Interpenetrating Polymer Networks: An Overview". Interpenetratin~ Polymer N~Lwolk~, edited by D. Klempner, L.H. Sperling, and L.A. Utracki, Advances in Chemistry Series #239, 3-38, 1994).

Materials having co-continuous phases may be made in accordance with the present invention by a number of different methods. Thus, for example, the polymeric first phase material may be mel~h~nically blended with the polymeric second phase material to achieve a co-continuous system. Examples of co-s continuous morphologies achieved by blending are described, for example, in D.
Bourry and B.D. Favis, "Co-Colllilluily and Phase Inversion in HDPEIPS Blends:
The Role of Interfacial Modification", 1995 Annual Technical Conference of the SocietY of Plastics Fn~in~ers ANTEC, Vol. 53, No. 2, 2001-2009 (polystyrene/polyethylene blends), and in A. Leclair and B.D. Favis, "The role of 0 interfacial contact in immiccihle binary polymer blends and its influence on meçh~nic~l ~r~c.lies", Polymer~ Vol. 37, No. 21, 4723-4728, 1996 (polycarbonate/polyethylene blends).
Co-continuous phases may also be forrned in accordance with the present invention by first by dissolving them out of ~upclclilical fluid extractions, such as that disclosed for blends of polystyrene and poly(methyl methacrylate) in U.S.
4,281,084, and then allowing them to phase separate following exposure to heat and/or m~rh~nical shear, as described by in N. Mekhilef, B.D. Favis and P.J.
Carreau, "Morphological Stability of Polystyrene Polyethylene Blends", 1995 Annual Technical Collfe.ence of the SocietY of Plastics Fngineçrs ANTEC, Vol.
53, No. 2, 1572-1579).
A further method of producing co-continuous phases in accordance with the present invention is through the creation of i~lhl~netrating polymer networks (IPNs). Some of the more hllpol~ll IPNs include simultaneous IPNs, sequential IPNs, gradient IPNs, latex IPNs, thermoplastic IPNs, and semi-IPNs. These and 2s other types of IPNs, their physical p~ ies (e.g., phase diagrams), and methods for their ~ alion and characterization, are described, for exarnple, in L.H.
Sperling and V. Mishra, "Current Status of Inl~l~enetrating Polymer Networks", PolYmers for Advanced Technolo~ies. Vol. 7, No. 4, 197-208, April 1996, and in L.H. Sperling, "Interpenetrating Polymer Networks: An Overview", Ill~ ,cnetratin~ Polymer Networks, edited by D. Kle"l~!ncl, L.H. Sperling, and W O 97/32225 PCT~US97/02995 L.A. Utracki, Advances in Chemistry Series #239, 3-38, 1994). Some ofthe major methods for pr~ g these systems are summarized below.
Simultaneous IPNs may be made by mixing together the respective monomers or prepolymers, plus the crosslinkers and activators, of two or more 5 polymer networks. The respective monomers or prepolymers are then reacted simultaneously, but in a non-i~ ,r~l;ng manner. Thus, for exarnple, one reactionmay be made to proceed by way of chain polymerization kinetics, and the other reaction may be made to proceed through step polymerization kinetics.
Sequential IPNs are made by first forming an initial polymer network.
lo Then, the monomers, cros~linkers, and activators of one or more additional networks are swollen into the initial polymer network, where they are reacted insitu to yield additional polymer networks.
Gradient IPNs are synth~si7ç~1 in such a manner that the overall composition or crosslink density of the IPN varies macroscopically in the material l s from one location to another. Such systems may be made, for example, by forming a first polymer network predo...i~ ly on one surface of a film and a second polymer network predominAntly on another surface of the film, with a gradient incomposition throughout the interior of the film.
Latex IPNs are made in the form of latexes (e.g., with a core and shell structure). In some variations, two or more latexes may be mixed and formed intoa film, which crosslink~ the polymers.
Thermoplastic IPNs are hybrids between polymer blends and IPNs that involve physical crosslinks instead of chemical crosslinks. As a result, these materials can be made to flow at elevated temp.ldlules in a manner similar to that 2s of thermoplastic elastomers, but are crosclinke(l and behave as IPNs at the telllpeld~ures of normal use.
Semi-IPNs are compositions of two or more polymers in which one or more of the polymers are crosslinked and one or more of the polymers are linear or brAn~
As indicated above, co-con~iiluiLy can be achieved in multicomponent systems as well as in binary systems. For example, three or more materials may be , .

W O 97/32225 PCTrUS97/02995 used in combination to give desired optical properties (e.g., tr~n~mi~sion and reflectivity) and/or improved physical pro~ lies. All coll.pol1ents may be immi~cible, or two or more co~ )onents may demonsLldle miscibility. A number of ternary systems exhibiting co-continuity are described, for example, in L.H.
Sperling, Chapter 1 "Interpenetrating Polymer Networks: An Overview", Interpenetratin~ Polymer Networks, edited by D. Klempner, L.H. Sperling, and L.A. Utracki, Advances in Chemistry Series #239, 3-38, 1994).
Char~cteri~tic sizes of the phase structures, ranges of volume fraction over which co-continuity may be observed, and stability of the morphology may all be 0 influenced by additives, such as compatibilizers, graft or block copolymers, or reactive colllpol1ents, such as maleic anhydride or glycidyl methacrylate. Such effects are described, for example, for blends of polystyrene and poly(ethylene terephth~l~te) in H.Y. Tsai and K. Min, "Reactive Blends of Functionalized Polystyrene and Polyethylene Terephth~l~te", 1995 Annual Technical Conference of the Society of Plastics Fnpin~ers ANTEC, Vol. 53, No. 2, 1858-1865.
However, for particular systems, phase diagrams may be constructed through routine experim~nt~tion and used to produce co-continuous systems in accordance with the present invention.
The microscopic structure of co-continuous systems made in accordance with the present invention can vary significantly, depending on the method of pl~p~dLion, the miscibility of the phases, the presence of additives, and other factors as are known to the art. Thus, for example, one or more of the phases in the co-continuous system may be fibrillar, with the fibers either randomly oriented or oriented along a common axis. Other co-continuous systems may comprise an open-celled matrix of a first phase, with a second phase disposed in a co-continuous manner within the cells of the matrix. The phases in these systems may be co-continuous along a single axis, along two axes, or along three axes.
Optical bodies made in accordance with the present invention and having co-continuous phases (particularly IPNs) will, in several in~t~nces, have properties that are advantageous over the ~ro~ lies of similar optical bodies that are madewith only a single continuous phase, depen-iin~, of course, on the properties of the W O 97/32225 PCT~US97/02995 individual polymers and the method by which they are combined. Thus, for example, the co-continuous systems of the present invention allow for the chemical and physical combination of structurally di~imil~r polymers, thereby providing aconvenient route by which the plU~Ut;l lies of the optical body may be modified to s meet specific needs. Furthermore, co-continuous systems will fre~uently be easier to process, and may impart such properties as weatherability, reduced fl~mm~bility, greater impact resistance and tensile strength, improved flexibility, and superior chemical resi~t~n-~e. IPNs are particularly advantageous in certainapplications, since they typically swell (but do not dissolve) in solvents, and lo exhibit suppressed creep and flow co~ ed to analogous non-IPN systems (see, e.g., D. Klempner and L. Berkowski, "Inlel~enetrating Polymer Ne;l~o~ks", Encyclopedia of Polymer Science and En~ineerin~. 2nd Ed., Vol. 9, 489-492.
One skilled in the art will ~p,~.,iate that the principles of co-continuous systems as are known to the art may be applied in light of the t~chin~ set forth15 herein to produce co-continuous morphologies having unique optical properties.
Thus, for example, the refractive indices of known co-continuous morphologies may be manipulated as taught herein to produce new optical films in accordance with the present invention. Likewise, the principles taught herein may be applied to known optical systems to produce co-continuous morphologies.
Thickness of Optical Body The thickness of the optical body is also an important parameter which can be manipulated to affect reflection and tr~n~mi~ion properties in the present invention. As the thickness of the optical body increases, diffuse reflection also 25 increases, and tr~n~mi~ion, both specular and diffuse, decreases. Thus, while the thickness of the optical body will typically be chosen to achieve a desired degree of mechanical strength in the fini.~h~(l product, it can also be used to directly to control reflection and tr~n.~mi~ion properties.
Thickness can also be utili~d to make final adjustments in reflection and 30 Il,...~...i~sion plol)~;,Lies of the optical body. Thus, for example, in filmapplications, the device used to extrude the film can be controlled by a downstream W O 9713222~ PCTrUS97/02995 optical device which measures tr~ncmi~ion and reflection values in the extruded film, and which varies the thickness of the film (i.e., by adjusting extrusion rates or ch~nging casting wheel speeds) so as to m~int~in the reflection and tr~n~mi~sionvalues within a pre~let~rmin~.l range.

Materials for Continuous/I)i~ e Phases Many different materials may be used as the continuous or disperse phases in the optical bodies of the present invention, depending on the specific application to which the optical body is directed. Such materials include i"olgal ic materials o such as silica-based polymers, organic materials such as liquid crystals, and polymeric materials, including monomers, copolymers, grafted polymers, and mixtures or blends thereof. The exact choice of m~tPri~l~ for a given application will be driven by the desired match and mi~m~trh obtainable in the refractive indices of the continuous and disperse phases along a particular axis, as well as the 5 desired physical plopcllies in the resulting product. However, the materials of the continuous phase will generally be characterized by being subst~nti~lly transparent in the region of the spectrum desired.
A further consideration in the choice of materials is that the resulting product must contain at least two distinct phases. This may be accomplished by 20 casting the optical material from two or more materials which are immiscible with each other. Alternatively, if it is desired to make an optical material with a first and second m~teri~l which are not immiscible with each other, and if the first material has a higher melting point than the second m~teri~l, in some cases it may be possible to embed particles of al~plo~,iate ~limencions of the first material25 within a molten matrix of the second material at a tclll~c.dlllre below the melting point of the first m~1eri~l The res..lting mixture can then be cast into a film, with or without subsequent orientation, to produce an optical device.
Suitable polymeric materials for use as the continuous or disperse phase in the present invention may be amorphous, semicryst~llin~7 or crystalline polymeric 30 materials, including materials made from monomers based on carboxylic acids such as isophthalic, ~elaic, adipic, sebacic, dibenzoic, terephth~l;c, 2,7-naphthalene dicarboxylic, 2,6-n~phth~lene dicarboxylic, cyclohexanedicarboxylic,and bibenzoic acids (including 4,4'-bibenzoic acid), or materials made from the corresponding esters of the aforementioned acids (i.e., dimethylterephth~l~te). Of these, 2,6-polyethylene n~phth~l~te (PEN) is especially prefelred because of itsstrain in~ ce(l birefringence, and because of its ability to remain permanently birefringent after stretching. PEN has a refractive index for polarized incident light of 550 nm wavelength which increases after stretching when the plane of polarization is parallel to the axis of stretch from about 1.64 to as high as about 1.9, while the refractive index decreases for light polarized perpendicular to the axis of lo stretch. PEN exhibits a birefringence (in this case, the clirr~lence between the index of refraction along the stretch direction and the index perpendicular to the stretch direction) of 0.25 to 0.40 in the visible spectrum. The birefringence can be increased by increasing the molecular orientation. PEN may be substantially heatstable from about 155~C up to about 230~C, depending upon the processing conditions utilized during the m~nl-f~tl~re ofthe film.
Polybutylene naphth~l~1e is also a suitable material as well as other crystalline naphthalene dicarboxylic polyesters. The crystalline n~phth~lene dicarboxylic polyesters exhibit a dirre~ ce in refractive indices associated with different in-plane axes of at least 0.05 and preferably above 0.20.
When PEN is used as one phase in the optical material of the present invention, the other phase is preferably polymethylmethacrylate (PMMA) or a syndiotactic vinyl a,~o,llatic polymer such as polystyrene (sPS). Other plef~lled polymers for use with PEN are based on terephthalic, isophthalic, sebacic, azelaic or cyclohexanedicarboxylic acid or the related alkyl esters of these materials.
Naphthalene dicarboxylic acid may also be employed in minor amounts to hll~love adhesion between the phases. The diol component may be ethylene glycol or a related diol. Preferably, the index of refraction of the selected polymer is less than about 1.65, and more preferably, less than about 1.55, although a similar result may be obtainable by using a polymer having a higher index of refraction if the sameindex difference is achieved.

Syndiotactic-vinyl aromatic polymers useful in the current invention include poly(styrene), poly(alkyl styrene), poly(styrene halide), poly(alkyl styrene), poly(vinyl ester benzoate), and these hydrogenated polymers and mixtures, or copolymers cont~ining these structural units. Examples of poly(alkyl styrenes) include: poly(methyl styrene), poly(ethyl styrene), poly(propyl styrene), poly(butyl styrene), poly(phenyl styrene), poly(vinyl naphth~lene), poly(vinylstyrene), and poly(acenaphthalene) may be mentioned. As for the poly(styrene halides), examples include: poly(chlorostyrene), poly(bromostyrene), and poly(fluorostyrene). Examples of poly(alkoxy styrene) include: poly(methoxy o styrene), and poly(ethoxy styrene). Among these examples, as particularly ~,efelable styrene group polymers, are: polystyrene, poly(p-methyl styrene), poly(m-methyl styrene), poly(p-tertiary butyl styrene), poly(p-chlorostyrene), poly(m-chloro styrene), poly(p-fluoro styrene), and copolymers of styrene and p-methyl styrene may be mentioned.
Furthermore, as comonomers of syndiotactic vinyl-aromatic group copolymers, besides monomers of above explained styrene group polymer, olefin monomers such as ethylene, propylene, butene, h~xene, or octene, diene monomers such as butadiene, isoprene; polar vinyl monomers such as cyclic diene monomer, methyl methacrylate, maleic acid anhydride, or acrylonitrile may be mentioned.
The syndiotactic-vinyl aromatic polymers of the present invention may be block copolymers, random copolymers, or alt~rn~ting copolymers.
The vinyl aromatic polymer having high level syndiotactic structure referred to in this invention generally includes polystyrene having syndiotacticity of higher than 75% or more, as determin~d by carbon-13 nuclear m~gn~tic resollallce. Preferably, the degree of syndiotacticity is higher than 85% racemic diad, or higher than 30%, or more preferably, higher than 50%, racemic pentad.
In addition, although there are no particular restrictions regarding the molecular weight of this syndiotactic-vinyl aromatic group polymer, preferably, the weight average molecular weight is greater than 10,000 and less than 1,000,000, and more preferably, greater than 50,000 and less than 800,000.

W O 97/32225 PCTrUS97/02995 As for said other resins, various types may be mentioned, including, for instance, vinyl ar~ alic group polymers with atactic structures, vinyl aromatic group polymers with isotactic structures, and all polymers that are miscible. For example, polyphenylene ethers show good miscibility with the previous explained s vinyl aromatic group polymers. Furthermore, the composition of these miscible resin components is preferably between 70 to I weight %, or more preferably, 50 to 2 weight %. When composition of miscible resin component exceeds 70 weight %, degradation on the heat re~i~t~nr~e may occur, and is usually not desirable.
lo It is not required that the selected polymer for a particular phase be a copolyester or copolycarbonate. Vinyl polymers and copolymers made from monomers such as vinyl naphthalenes, styrenes, ethylene, maleic anhydride, acrylates, and meth~rrylates may also be employed. Conden~tion polymers, other than polyesters and polycarbonates, can also be ~ltili7efl Suitable con-1.?n~tion polymers include polysulfones, poly~mi~les~ polyulcLhalles, polyamic acids, and polyimides. Naphthalene groups and halogens such as chlorine, bromine and iodine are useful in increasing the refractive index of the selected polymer to the desired level (1.59 to 1.69) if needed to substantially match the refractive index if PEN is the host. Acrylate groups and fluorine are particularly useful in decreasing the refractive index.
Minor amounts of comonomers may be substituted into the n~phth~lene dicarboxylic acid polyester so long as the large refractive index difference in the orientation direction(s) is not subst~nti~lly coll~pro~lised. A smaller index difference (and therefore decreased reflectivity) may be counterbalanced by 2s advantages in any of the following: improved adhesion between the continuous and disperse phase, lowered telllpeld~ure of extrusion, and better match of meltviscosities.

Region of Spectrum While the present invention is frequently described herein with reference to the visible region of the spectrum, various embodiments of the present invention can be used to operate at dirr~l~nt wavelengths (and thus frequencies) of electrom~gnetic radiation through applo~l;ate scaling ofthe co~ o~ ts ofthe optical body. Thus, as the wavelength increases, the linear size of the components of the optical body may be increased so that the dimensions of these components,s measured in units of wavelength, remain approximately constant.
Of course, one major effect of t~h~nging wavelength is that, for most materials of interest, the index of refraction and the absorption coefficient change.
However, the principles of index match and mi~m~t~h still apply at each wavelength of interest, and may be utilized in the selection of materials for anlo optical device that will operate over a specific region ofthe ~I,ecll~n. Thus, for example, proper scaling of ~iim~n~ions will allow operation in the infrared, near-ultraviolet, and ultra-violet regions of the spectrurn. In these cases, the indices of refraction refer to the values at these wavelengths of operation, and the body thickness and size of the disperse phase scalh,;ilg components should also be 15 approximately scaled with wavelength. Even more of the electrom~gn~-tic spectrum can be used, including very high, ultrahigh, microwave and millimeter wave frequencies. Polarizing and diffusing effects will be present with proper scaling to wavelength and the indices of refraction can be obtained from the square root of the dielectric function (including real and im~gin~ry parts). Useful products 20 in these longer wavelength bands can be diffuse reflective polarizers and partial polarizers.
In some embo-lim~ntc of the present invention, the optical properties of the optical body vary across the wavelength band of interest. In these embo~iim~nt~
materials may be utilized for the continuous and/or disperse phases whose indices 25 of refraction, along one or more axes, varies from one wavelength region to another. The choice of continuous and disperse phase materials, and the optical pl~c.lies (i.e., diffuse and disperse reflection or specular tr~n~mi~sion) resl.lting from a specific choice of materials, will depend on the wavelength band of interest.

W O 97/32225 PCT~US97102995 Skin Layers A layer of material which is subst~nti~11y free of a disperse phase may be coextensively disposed on one or both major surfaces of the film, i.e., the extruded blend of the disperse phase and the continuous phase. The composition of the s layer, also called a skin layer, may be chosen, for example, to protect the integrity of the disperse phase within the extruded blend, to add mechanical or physical properties to the final film or to add optical functionality to the final film. Suitable materials of choice may include the material of the continuous phase or the material of the disperse phase. Other m~t~ri~l~ with a melt viscosity similar to the 10 extruded blend may also be useful.
A skin layer or layers may reduce the wide range of shear intensities the extruded blend might experience within the extrusion process, particularly at the die. A high shear environment may cause undesirable surface voiding and may result in a textured surface. A broad range of shear values throughout the thickness 15 of the film may also prevent the disperse phase from forming the desired particle size in the blend.
A skin layer or layers may also add physical strength to the resulting composite or reduce problems during procec~ing, such as, for example, reducing the tendency for the film to split during the orientation process. Skin layer 20 materials which remain amorphous may tend to make films with a higher tollghn~ss, while skin layer materials which are semicrystalline may tend to make films with a higher tensile modulus. Other functional components such as ~nti~tAtic additives, UV absorbers, dyes, antioxi~l~nts~ and pigments, may be added to the skin layer, provided they do not subst~nti~lly hlle.~le with the desired 25 optical properties of the resllltin~ product.
Skin layers or coatings may also be added to impart desired barrier p,o~ lies to the resulting film or device. Thus, for example, barrier films or coatings may be added as skin layers, or as a component in skin layers, to alter the .-,is~ive properties ofthe film or device towards liquids, such as water or 30 organic solvents, or gases, such as oxygen or carbon dioxide.

Skin layers or coatings may also be added to impart or improve abrasion reSict~nce in the resulting article. Thus, for example, a skin layer comprising particles of silica embedded in a polymer matrix may be added to an optical filmproduced in accordance with the invention to impart abrasion resistance to the film, 5 provided, of course, that such a layer does not unduly colllplolnise the optical properties required for the application to which the film is directed.
Skin layers or coatings may also be added to impart or improve puncture and/or tear resiet~nce in the resulting article. Thus, for example, in embo-limPnte in which the outer layer of the optical film contains coPEN as the major phase, a o skin layer of monolithic coPEN may be coextruded with the optical layers to impart good tear resiet~nce to the resulting film. Factors to be considered in selecting a material for a tear reci et~nt layer include percent elongation to break, Young's modulus, tear strength, adhesion to interior layers, percent LldllsllliLl~lce and absorbance in an electrom~gnetic bandwidth of interest, optical clarity or h~e, 5 refractive indices as a function of frequency, texture and rol-ghness, melt thermal stability, molecular weight distribution, melt rheology and coextrudability, miscibility and rate of inter-diffusion between materials in the skin and optical layers, viscoelastic response, relaxation and cryst~lli7~tion behavior under draw conditions, therm~l stability at use tclllp~ s, weatherability, ability to adhere to 20 coatings and permeability to various gases and solvents. Puncture or tear resistant skin layers may be applied during the m~nllf~tllring process or later coated onto or l~min~tP~l to the optical film. Adhering these layers to the optical film during the m~nllf~-~turing process, such as by a coextrusion process, provides the advantage that the optical film is protected during the m~m]f~cturing process. ln some 25 embo-iimPnte, one or more puncture or tear resi~t~nt layers may be provided within the optical film, either alone or in combination with a puncture or tear resistant skin layer.
The skin layers may be applied to one or two sides of the extruded blend at some point during the extrusion process, i.e., before the extruded blend and skin 30 layer(s) exit the extrusion die. This may be accompliehe(l using conventionalcoextrusion technology, which may include using a three-layer coextrusion die.

T ~min~tion of skin layer(s) to a previously formed film of an extruded blend is also possible. Total skin layer thicknesses may range from about 2% to about 50% of the total blend/skin layer thickness.
In some applications, additional layers may be coextruded or adhered on 5 the outside of the skin layers during m~nl1f~ct11re of the optical films. Suchadditional layers may also be extruded or coated onto the optical film in a separate coating operation, or may be l~ n~tecl to the optical film as a separate film, foil, or rigid or semi-rigid substrate such as polyester (PET), acrylic (PMMA), polycarbonate, metal, or glass.
lo A wide range of polymers are suitable for skin layers. Of the predomin~ntly amorphous polymers, suitable examples include copolyesters based on one or more of terephthalic acid, 2,6-naphthalene dicarboxylic acid, isophthalic acid phthalic acid, or their alkyl ester counterparts, and alkylene diols, such as ethylene glycol. Examples of semicrystalline polymers suitable for use in skin 15 layers include 2,6-polyethylene n~phth~l~te, polyethylene terephth~l~t~, and nylon materials. Skin layers that may be used to increase the tol1ghn~ s~ of the optical film include high elongation polyesters such as EcdelTM and PCTG 5445 (availablecommercially from Eastman Chemical Co., Rochester, N.Y.) and polyc~l~ona~es.
Polyolefins, such as polypropylene and polyethylene, may also be used for this 20 purpose, especially if they are made to adhere to the optical film with a compatibilizer .

Functional layers Various functional layers or coatings may be added to the optical films and 25 devices of the present invention to alter or improve their physical or chemical ~rop~,lies, particularly along the surface of the film or device. Such layers orcoatings may include, for example, slip agents, low adhesion backside materials,CO~ ctive layers, ~ntist~tic coatings or films, barrier layers, flame retardants, UV
stabilizers, abrasion resistant m~t~ri~l~, optical coatings, or substrates designed to 30 improve the mechanical hl~egl;ly or strength of the film or device.

., ... .. "

W O 97/32225 PCT~US97102995 The films and optical devices of the present invention may be given good slip plopellies by treating them with low friction coatings or slip agents, such as polymer beads coated onto the surface. Alternately, the morphology of the surfaces of these materials may be modified, as through manipulation of extrusion conditions, to impart a slippery surface to the film; methods by which surface morphology may be so modified are described in U.S. Serial Number 08/612,710.
In some applications, as where the optical films of the present invention are to be used as a component in adhesive tapes, it may be desirable to treat the films with low adhesion b~ç~i7~ (LAB) co~ting~ or films such as those based on o urethane, silicone or fluorocarbon ch~mi~try. Films treated in this manner will exhibit proper release pl~,l)ellies towards pressure sensitive adhesives (PSAs),thereby enabling them to be treated with adhesive and wound into rolls. Adhesivetapes made in this manner can be used for decorative purposes or in any application where a diffusely reflective or tr~n~mi~ive surface on the tape is s desirable.
The films and optical devices of the present invention may also be provided with one or more conductive layers. Such conductive layers ma~ comprise metals such as silver, gold, copper, alllmimlm,chlollliulll, nickel, tin, and titanium, metal alloys such as silver alloys, stainless steel, and inconel, and semiconductor metal oxides such as doped and undoped tin oxides, zinc oxide, and indium tin oxide (ITO).
The films and optical devices of the present invention may also be provided with ~nti~t~tic co~ting.~ or films. Such coatings or films include, for example, V2O5 and salts of sulfonic acid polymers, carbon or other conductive metal layers.
The optical films and devices of the present invention may also be provided with one or more barrier films or co~ting~ that alter the tr~n~mi~sive properties of the optical film towards certain liquids or gases. Thus, for example, the devices and films of the present invention may be provided with films or coatings that inhibit the Ll~ sion of water vapor, organic solvents, ~2~ or CO2 through the film. Barrier co~ting~ will be particularly desirable in high humidity environment~, where components of the film or device would be subject to distortion due to moisture permeation.
The optical films and devices of the present invention may also be treated with flame retardants, particularly when used in environment~, such as on airplanes, that are subject to strict fire codes. Suitable flame retardants include ahlminllm trihydrate, antimony trioxide, antimony pentoxide, and flame le~dillg organophosphate compounds.
The optical films and devices of the present invention may also be provided with abrasion-resi~t~nt or hard coatings, which will frequently be applied as a skin o layer. These include acrylic hardcoats such as Acryloid A-l 1 and Paraloid K-120N, available from Rohm & Haas, Philadelphia, PA; urethane acrylates, such as those described in U.S. Pat. No. 4,249,011 and those available from Sartomer Corp., Westçh~st~r, PA; and urethane hardcoats obtained from the reaction of an aliphatic polyisocyanate (e.g., Desmodur N-3300, available from Miles, Inc., PiL~sl)~gh, PA) with a polyester (e.g., Tone Polyol 0305, available from Union Carbide, Houston, TX).
The optical films and devices of the present invention may further be l~min~te~l to rigid or semi-rigid sub:,ka~es, such as, for example, glass, metal, acrylic, polyester, and other polymer b~rl~ingc to provide structural rigidity, weatherability, or easier h~ntlling. For example, the optical films of the present invention may be l~minz~tecl to a thin acrylic or metal backing so that it can be stamped or otherwise formed and m~int~in~-1 in a desired shape. For some applications, such as when the optical film is applied to other breakable b~cl~ingc, an additional layer comprising PET film or puncture-tear resistant film may be used.
The optical films and devices of the present invention may also be provided with shatter resi~t~nt films and co~ting.c. Films and coatings suitable for thispurpose are described, for example, in publications EP 592284 and EP 591055, andare available commercially from 3M Compdlly, St. Paul, MN.
Various optical layers, m~teri~lc, and devices may also be applied to, or used in conjunction with, the films and devices of the present invention for specific W O 97/32225 PCTrUS97/02995 applications. These include, but are not limited to, m~gnetic or m~gneto-optic co~ting~ or films; liquid crystal panels, such as those used in display panels and privacy windows; photographic emulsions; fabrics; prismatic films, such as linear Fresnel lenses; brightness çnh~ncement films; holographic films or images;
s embossable films; anti-tamper films or co~fing~; IR transparent film for low emissivity applications; release films or release coated paper; and polarizers or mirrors.
Multiple additional layers on one or both major surfaces of the optical film are contemplated, and can be any combination of afo~ lllioned coatings or films.o For example, when an adhesive is applied to the optical film, the adhesive maycontain a white pigment such as titanium dioxide to increase the overall reflectivity, or it may be optically transparent to allow the reflectivity of the substrate to add to the reflectivity of the optical film.
In order to improve roll formation and convertibility of the film, the optical 15 films of the present invention may also comprise a slip agent that is incorporated into the film or added as a separate coating. In most applications, slip agents will be added to only one side of the film, ideally the side facing the rigid substrate in orderto ~ lillli7f' h~e.

20 Microvoiding In some embo-liment~, the materials of the continuous and disperse phases may be chosen so that the int~ ce between the two phases will be sufficiently weak to result in voiding when the film is oriented. The average dimensions of the voids may be controlled through careful manipulation of processing parameters 2s and stretch ratios, or through selective use of compatibilizers. The voids may be back-filled in the fini~h~l product with a liquid, gas, or solid. Voiding may beused in conjunction with the aspect ratios and refractive indices of the disperse and continuous phases to produce desirable optical properties in the resulting film.

-3s-W 097/32225 PCTrUS97/02995 More Than Two Phases The optical bodies made in accordance with the present invention may also consist of more than two phases. Thus, for example, an optical material made in accordance with the present invention can consist of two dirr~,lent disperse phases 5 within the continuous phase. The second disperse phase could be randomly or non-randomly dispersed throughout the continuous phase, and can be randomly aligned or aligned along a common axis.
Optical bodies made in accor~1a,lce with the present invention may also consist of more than one continuous phase. Thus, in some embodiments, the 0 optical body may include, in addition to a first continuous phase and a disperse phase, a second phase which is co-continuous in at least one dimension with the first continuous phase. In one particular embo-lim~nt, the second continuous phase is a porous, sponge-like material which is coextensive with the first continuousphase (i.e., the first continuous phase extends through a network of ch~nnel~ orspaces exten~ing through the second continuous phase, much as water extends through a network of channels in a wet sponge). In a related embodiment, the second continuous phase is in the form of a dendritic structure which is coextensive in at least one tlimemion with the first continuous phase.

20 Multilayer Combinations If desired, one or more sheets of a continuous/disperse phase film made in accordance with the present invention may be used in combination with, or as a component in, a multilayered film (i.e., to increase reflectivity~. Suitable multilayered films include those of the type described in WO 95/17,303 (O~ldçrkirk 25 et al.). In such a construction, the individual sheets may be l~min~tecl or otherwise adhered together or may be spaced apart. If the optical thicknesses of the phases within the sheets are subst~nti~lly equal (that is, if the two sheets present a s1lhst~nti~lly equal and large number of scatterers to incident light along a given axis), the composite will reflect, at somewhat greater efficiency, substantially the 30 same band width and spectral range of reflectivity (i.e., "band") as the individual sheets. If the optical thicl~n~s~es of phases within the sheets are not subst~nti~lly W O 97/3222S PCTrUS97/02995 equal, the composite will reflect across a broader band width than the individual phases. A composite combining mirror sheets with polarizer sheets is useful for increasing total reflectance while still polarizing tr~n~mittecl light. Al~ Li~tely, a single sheet may be asymmetrically and biaxially oriented to produce a film having s selective reflective and pol~ri7ing pro~c,lies.
FIG. 5 illustrates one example of this embodiment of the present invention.
There, the optical body consists of a multilayer film 20 in which the layers ~Itern~te between layers of PEN 22 and layers of co-PEN 24. Each PEN layer includes a disperse phase of syndiotactic polystyrene (sPS) within a matrix of PEN.
o This type of construction is desirable in that it promotes lower off-angle color.
Furthermore, since the layering or inclusion of scalL~ averages out light leakage, control over layer thic~n~c~ is less critical, allowing the film to be more tolerable of variations in proces~ing parameters.
Any of the m~teri~l~ previously noted may be used as any of the layers in 5 this embodiment, or as the continuous or disperse phase within a particular layer.
However, PEN and co-PEN are particularly desirable as the major coll~ponents of cçrlt layers, since these materials promote good laminar a&esion.
Also, a number of variations are possible in the arrangement of the layers.
Thus, for example, the layers can be made to follow a repeating sequence through20 part or all of the structure. One example of this is a construction having the layer pattern ... ABCABC ..., wherein A, B, and C are distinct m~t~ri~l~ or distinct blends or mixLu,~s of the same or dirrelcllL materials, and wherein one or more of A, B, or C con~ s at least one disperse phase and at least one continuous phase.The skin layers are preferably the same or chemically similar m~t~ri~
Antirefl~ t~Qn Layers The films and other optical devices made in accordance with the invention may also include one or more anti-reflective layers or co~ting~ such as, for example, convention~l vacuum coated dielectric metal oxide or metaVmetal oxide 30 optical films, silica sol gel co~tinE~ and coated or coextruded antireflective layers such as those derived from low index fluoropolymers such as THV, an extrudable W O 97132225 PCT~US97/02995 fluoropolymer available from 3M Company (St. Paul, MN). Such layers or coatingc, which may or may not be polarization sensitive, serve to increase tr~n~mi~sion and to reduce reflective glare, and may be imparted to the films and optical devices of the present invention through aypl~pliate surface treatment, such s as coating or sputter etching. A particular example of an antireflective coating is described in more detail in Examples 132-133.
In some embo-lim~nt~ of the present invention, it is desired to maximize the tr~n~mi~cion and/or minimi7~ the specular reflection for certain polarizations of light. In these embo-liment~, the optical body may comprise two or more layers in o which at least one layer comprises an anti-reflection system in close contact with a layer providing the continuous and disperse phases. Such an anti-reflection system acts to reduce the specular reflection of the incident light and to increase theamount of incident light that enters the portion of the body comprising the continuous and disperse layers. Such a function can be accomplished by a varietyof means well known in the art. Examples are quarter wave anti-reflection layers, two or more layer anti-reflective stack, graded index layers, and graded densitylayers. Such anti-reflection functions can also be used on the transmitted lightside of the body to increase transmitted light if desired.

Anti-Fog Layers The films and other optical devices made in accordance with the invention may be provided with a film or coating which imparts anti-fogging properties. Insome cases, an anti-reflection layer as described above will serve the dual purpose of hlly~~ g both anti-reflection and anti-fogging yroy~llies to the film or device.
2s Various anti-fogging agents are known to the art which are suitable for use with the present invention. Typically, however, these materials will substances, such as fatty acid esters, which impart hydrophobic ylol~el Lies to the film surface andwhich promote the formation of a continuous, less opaque film of water.
Coatings which reduce the tendency for surfaces to "fog" have been reported by several inventors. For example, U.S. Patent No. 3,212,909 to Leigh discloses the use of ammonium soap, such as aL~yl amrnoniurn carboxylates in . .

admixture with a surface active agent which is a sulfated or sulfonated fatty matterial, to produce a anti-fogging composition. U.S. Patent No. 3,075,228 to Elias discloses the use of salts of sulfated alkyl aryloxypolyalkoxy alcohol, as well as alkylbenzene sulfonates, to produce an anti-fogging article useful in cleaning 5 and imparting anti-fogging properties to various surfaces. U.S. Patent No.
3,819,522 to Zmoda, discloses the use of surfactant combinations comprising derivatives of decyne diol as well as surfactant mixtures which include ethoxylated alkyl sulfates in an anti-fogging window cleaner surfactant mixture. J~p~nese Patent Kokai No. Hei 6[1994]41,335 discloses a clouding and drip preventive lo composition comprising colloidal alumina, colloidal silica and an anionic surfactant. U.S. Patent No. 4,478,909 (Taniguchi et al) discloses a cured anti-fogging coating film which comprises polyvinyl alcohol, a finely divided silica,and an organic silicon compound, the carbon/silicon weight ratio al~part,ntly ebing hnl~ollallL to the film's reported anti-fogging pro~ lies. Various surf~t~nt~, s include fluorine-cont~ining s~ t~nt~, may be used to improve the surface smoothness of the coating. Other anti-fog coatings incorporating surf~ct~nt~ aredescribed in U.S. Patents 2,803,552; 3,022,178; and 3,897,356. World Patent No.
PCT 96/18,691 (Scholtz et al) discloses means by which coatings may impart both anti-fog and anti-reflective properties.
UV Pr~tective Layers The films and optical devices of the present invention may be protected from UV radiation through the use of UV stabilized films or coatings. Suitable UV
stabilized films and coating~ include those which incorporate benzotri~oles or 25 hindered amine light stabilizers (HALS) such as TinuvinTM 292, both of which are available commercially from Ciba Geigy Corp., Hawthorne, NY. Other suitable W stabilized films and co~ting~ include those which contain benzophenones or diphenyl acrylates, available commercially from BASF Corp., P~ip~ y, NJ.
Such films or coatings will be particularly important when the optical films and30 devices of the present invention are used in outdoor applications or in luminaires where the source emits significant light in the UV region of the spectrum.

wo 97l32225 PCT/USg7/02995 Surface Treatments The films and other optical devices made in accordance with the present invention may be subjected to various treatments which modify the surfaces of these materials, or any portion thereof, as by rendering them more conducive to subsequent tre~tm~nt~ such as coating, dying, met~lli7ing, or l~min~tion. This may be accomplished through tre~tm~r~t with primers, such as PVDC, PMMA, epoxies, and aziridines, or through physical priming tre~tm~nt~ such as corona, flame, plasma, flash lamp, sputter-etching, e-beam treatments, or amorphizing the surface lo layer to remove crystallinity, such as with a hot can.

Lubricants Various lubricants may be used during the processing (e.g., extrusion) of the films of the present inven~ion. Suitable lubricants for use in the present invention include calcium sterate, zinc sterate, copper sterate, cobalt sterate,molybdenum neodoc~no~te, and ruthenium (III) acetylacetonate.

Antioxidants Antioxidants usefill in the present invention include 4,4'-thiobis-(6-t-butyl-m-cresol), 2,2'-methylenebis-(4-methyl-6-t-butyl-butylphenol), octadecyl-3,5-di-t-butyl-4-hydroxyhydrocinn~m~te, bis-(2,4-di-t-butylphenyl) pentaerythritol diphosphite, IrganoxTM 1093 (1979)(((3,5 -bis( l,1 -dimethylethyl)-4-hydroxyphenyl)methyl)-dioctadecyl ester phosphonic acid), IrganoxTM 1098 (N,N'-1,6-hexanediylbis(3,5-bis(1,1 -dimethyl)-4-hydroxy-benzenepropanarnide), NaugaardTM 445 (aryl amine), IrganoxTM L 57 (alkylated diphenylamine), IrganoxTML 115 (sulfur co. .t~ ,g bisphenol), IrganoxT~ LO 6 (alkylated phenyl-delta-napthylamine), Ethanox 398 (flourophosphonite), and 2,2'-ethylidenebis(4,6-di-t-butylphenyl)fluorophosnite .
A group of antioxidants that are especially l.-er.,lled are sterically hindered phenols, including butylated hydroxytoluene (BHT), Vitamin E (di-alpha-tocopherol), IrganoxTM 1425WL(calcium bis-(O-ethyl(3,5-di-t-butyl-4-.. ~ .. . . . .

WO 97/32225 PCTIUS97tO2995 hydroxybenzyl))phosphonate), IrganoxTM 1010 (tetrakis(methylene(3,5,di-t-butyl-4-hydroxyhydrocinn~m~te))meth~ne), IrganoxTM 1076 (octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinn~m~te), Fth~noxTM 702 (hindered bis phenolic), Etanox 330 (high molecular weight hindered phenolic), and EthanoxTM 703 (hindered phenolic 5 amme).

Dyes, Pigments, Inks, and Imaging Layers The films and optical devices of the present invention may be treated with inks, dyes, or pigm~nt~ to alter their appearance or to customize them for specific o applications. Thus, for example, the films may be treated with inks or other printed indicia such as those used to display product identification, adverti~ement~, w~rning~, decoration, or other information. Various techniques can be used to print on the film, such as sc~ hl~ing, l~LIel~less, offset, flexographic printing, stipple printing, laser printing, and so forth, and various types of ink can be used, 5 including one and two component inks, oxidatively drying and UV-drying inks, dissolved inks, dispersed inks, and 100% ink systems.
The a~,~e~al~ce of the optical film may also be altered by coloring the film, such as by l~min~tin~ a dyed film to the optical film, applying a pi~mentecl coating to the surface of the optical film, or including a pigment in one or more of the20 materials (e.g., the continuous or disperse phase) used to make the optical film.
Both visible and near IR dyes and pigmentc are contemplated in the present invention, and include, for example, optical brightçn~rs such as dyes that absorb in the W and fluoresce in the visible region of the color spectrum. Other additional layers that may be added to alter the appea-dllce of the optical film include, for 25 example, opacifying (black) layers, diffusing layers, holographic images or holographic diffusers, and metal layers. Each of these may be applied directly to one or both surfaces of the optical film, or may be a component of a second film or foil construction that is l~min~te~l to the optical film. ~ltPrn~tely, some components such as opacifying or diffusing agents, or colored pigmçnt~, may be 30 included in an adhesive layer which is used to l~min~te the optical film to another surface.

W O 97132225 PCT~US97/02995 The films and devices of the present invention may also be provided with metal co~1ing~. Thus, for example, a metallic Iayer may be applied directly to the optical film by pyrolysis, powder coating, vapor deposition, cathode sputtering, ion plating, and the like. Metal foils or rigid metal plates may also be 1~ e(l to the s optical film, or separate polymeric films or glass or plastic sheets may be first metallized using the aforementioned techniques and then l~min~Pd to the optical films and devices of the present invention.
Dichroic dyes are a particularly useful additive for many of the applications to which the films and optical devices of the present invention are directed, due to lo their ability to absorb light of a particular polarization when they are molecularly aligned within the material. When used in a film or other m~t~ri~l which predomin~ntly scatters only one polarization of light, the dichroic dye causes the material to absorb one polarization of light more than another. Suitable dichroic dyes for use in the present invention include Congo Red (sodium diphenyl-bis-a-s naphthylamine sulfonate), methylene blue, stilbene dye (Color Index (CI) = 620), and l,l'-diethyl-2,2'-cyanine chloride (CI = 374 (orange) or CI = 518 (blue)). The properties of these dyes, and methods of m~kin~ them, are described in E.H. Land, Colloid Chemistry (1946). These dyes have noticeable dichroism in polyvinyl alcohol and a lesser dichroism in cellulose. A slight dichroism is observed with20 Congo Red in PEN.

Other suitable dyes include the following materials:

(l) R~R

h Ri ~ ~ ' l CH=N--O

~O--CgHI9 o OH

(4~ ~ ~N--CH2 O NH2 ~
The l),u~ellies of these dyes, and methods of making them, are discussed in the Kirk Othmer Encyclopedia of Chemical Technology, Vol. 8, pp. 652-661 (4th Ed.
5 1993), and in the references cited therein.
When a dichroic dye is used in the optical bodies of the present invention, it may be incGl~u,~led into either the continuous or disperse phase. However, it isplerell~d that the dichroic dye is hlcol~oldled into the disperse phase.

W O 97/32225 PCT~US97/02995 I)ychroic dyes in combination with certain polymer systems exhibit the ability to polarize light to varying degrees. Polyvinyl alcohol and certain dichroic dyes may be used to make films with the ability to polarize light. Other polymers, such as polyethylene terephth~l~te or poly~mi~le~, such as nylon-6, do not exhibit s as strong an ability to polarize light when combined with a dichroic dye. The polyvinyl alcohol and dichroic dye combination is said to have a higher dichroism ratio than, for example, the same dye in other film forming polymer systems. A
higher dichroism ratio indicates a higher ability to polarize light.
Molecular ~lignment of a dichroic dye within an optical body made in o accordance with the present invention is preferably accomplished by stretching the optical body after the dye has been incorporated into it. However, other methodsmay also be used to achieve molecular ~ nment Thus, in one method, the dichroic dye is cryst~lli7~rl as through sublimation or by cryst~lli7~tion from solution, into a series of elong~te~l notches that are cut, etched, or otherwise formed 15 in the surface of a film or other optical body, either before or after the optical body has been oriented. The treated surface may then be coated with one or more surface layers, may be incol~laled into a polymer matrix or used in a multilayerstructure, or may be utilized as a component of another optical body. The notches may be created in accordance with a predetermin~l pattern or diagram, and with a20 predetermined amount of spacing between the notches, so as to achieve desirable optical properties.
In a related emborliment, the dichroic dye may be disposed within one or more hollow fibers or other conduits, either before or after the hollow fibers or conduits are disposed within the optical body. The hollow fibers or conduits may25 be constructed out of a material that is the same or dirrt;l~llt from the surrounding m~teri~l of the optical body.
In yet another embo~liment the dichroic dye is disposed along the layer interface of a multilayer construction, as by sublimation onto the surface of a layer before it is inco.~oraled into the multilayer construction. In still other 30 embo-lim~nte, the dichroic dye is used to at least partially backfill the voids in a microvoided film made in accordance with the present invention.

Adhesives Adhesives may be used to l~nnin~te the optical films and devices of the present invention to another film, surface, or substrate. Such adhesives include5 both optically clear and diffuse adhesives, as well as pleS~ e sensitive and non-pressure sensitive adhesives. Pressure sensitive adhesives are normally tacky atroom te~ dlule and can be adhered to a surface by application of, at most, lightfinger pressure, while non-l.les~ule sensitive adhesives include solvent, heat, or radiation activated adhesive systems. Examples of adhesives useful in the present o invention include those based on general compositions of polyacrylate; polyvinyl ether; diene-co..~ il-g rubbers such as natural rubber, polyisoprene, and polyisobutylene; polychlorol)lene; butyl rubber; b~lt~-liene-acrylonitrile polymers thermoplastic el&~lo~ , block copolymers such as styrene-isoprene and styrene-isoprene-styrene block copolymers, ethylene-propylene-diene polymers, and styrene-butadiene polymers; polyalphaolefins; amorphous polyolefins; silicone;
ethylene-cot~ g copolymers such as ethylene vinyl acetate, ethylacrylate, and ethylmethacrylate; polyureth~n~s; polyamides; polyesters; epoxies;
polyvinylpyrrolidone and vinylpyrrolidone copolymers; and mixtures of the above.Additionally, the adhesives can contain additives such as tackifiers, plasticizers, fillers, antioxidants, stabilizers, pjgm~nt~, diffusing particles,curatives, and solvents. When a l~min~ting adhesive is used to adhere an opticalfilm of the present invention to another surface, the adhesive composition and thickness are preferably selected so as not to hll~ e with the optical plop. . lies of the optical film. For example, when l~min~ting additional layers to an optical 2s polarizer or mirror wherein a high degree of tr~ncm~ on is desired, the l~min~ting adhesive should be optically clear in the wavelength region that the polarizer or mirror is designe(l to be transparent in.

Other Additives In addition to the films, coatings, and additives noted above, the opticaL
m~t~ri~l~ of the present invention may also comprise other materials or additives as are known to the art. Such materials include binders, coatings, fillers, compatibilizers, surf~ct~nt~, antimicrobial agents, foaming agents, reillfolccl~, heat stabilizers, impact modifiers, plasticizers, viscosity modifiers, and other such m~ter~

Applications of Present Invention The optical bodies of the present invention are particularly useful as diffuse polarizers. However, optical bodies may also be made in accordance with the invention which operate as reflective polarizers or diffuse mirrors. In these o applications, the construction of the optical material is similar to that in the diffuser applications described above. However, these reflectors will generally have a much larger dirr~,lence in the index of refraction along at least one axis. This index dir~l~llce is typically at least about 0.1, more pref~l~bly about 0.15, and mostpreferably about 0.2.
s Reflective polarizers have a l~rld~ e index ~lirr~;lellce along one axis, and subst~nti~lly m~trhe(l indices along another. Reflective films, on the other hand, differ in refractive index along at least two in-film plane orthogonal axes.
However, the reflective ~lOp~,l lies of these embo~liment~ need not be ~tt~in solely by reliance on refractive index mi~m~tchP~. Thus, for example, the thickness of the films could be adjusted to attain a desired degree of reflection. In some cases, adjustment of the thickness of the film may cause the film to go from being a tr~ncmi~ive difrustil to a diffuse reflector.
The reflective polari~r of the present invention has many different applications, and is particularly useful in liquid crystal display panels. In addition, the polarizer can be constructed out of PEN or similar m~tt~ri~ls which are goodultraviolet filters and which absorb ultraviolet light efficiently up to the edge of the visible spectrum. The reflective polarizer can also be used as a thin infrared sheet polarlzer.

W O 97/32225 PCTrUS97tO2995 Fenestrations The optical films and devices of the present invention are suitable for use in fenestrations, such as skylights or privacy windows, where diffuse tr~nemi~.eion of light is desirable and trans~ cy or clarity of the fenestration is either 5 ~ cess~. y or undesirable. In such applications, the optical films of the present invention may be used in conjunction with, or as components in, conventional glazing materials such as plastic or glass. Glazing materials ple~ d in this manner can be made to be polarization specific, so that the fenestration is ee.e~nti~lly transparent to a first polarization of light but subst~nti~lly reflects a lo second polarization of light, thereby elimin~ting or red~lcing glare. The physical properties of the optical films can also be modified as taught herein so that the glazing materials will reflect light of one or both polarizations within a certain region of the spectrum (e.g., the UV region), while L~ . ..i 11 ;ng light of one or both polarizations in another region (e.g., the visible region).
The optical films of the present invention may also be used to provide decorative fenestrations which transmit light of specific wavelengths. Such fenestrations may be used, for example, to impart a specific color or colors to a room (e.g., blue or gold), or may be used to accent the decor thereof, as through the use of wavelength specific lighting panels.
The optical films of the present invention may be incorporated into glazing materials in various manners as are known to the art, as through coating or extrusion. Thus, in one embodiment, the optical films are a&ered to all, or a portion, of the outside surface of a glazing material, either by l~min~tion or with the use of an optical adhesive. In another embodiment, the optical films of the present invention are sandwiched between two panes of glass or plastic, and the resulting composite is incorporated into a fenestration. Of course, the optical film may be given any additional layers or coatings (e.g., UV absorbing layers, antifogging layers, or antireflective layers) as are described herein to render it more suitable for the specific application to which it is directed.

~7-Light Fixtures The optical films of the present invention may be used in various light fixture applications, especially those in which polarized emitted light is plef~lred.
A typical light fixture contains a light source and various other elements which5 may include a reflective element (typically placed behind the light source), apo1~ri7ing element (typically positioned at the output ofthe light fixture), and a diffusing element that obscures the light source from direct viewing. These elements may be arranged in various configurations within a housing as dictated by aesthetic and/or functional considerations.
lo The light sources most suitable for use with the optical films ofthe present invention are diffuse light sources which emit light having a high degree of scatter or randomization with respect to both polarization and direction. Such diffuse sources preferably include a light emitting region and a light reflecting, scattering, and/or depolarizing region. Depending upon the particular application to which the light fixture is directed, the diffuse source may be a fluorescent larnp, an inc~n~escçnt lamp, a solid-state source or electrol~min~scçnt (EL) light source, or a metal halide lamp. The source may also be a randomi7ing, depolarizing surface used in combination with a point light source, a distant light source, or even solar illumination, the later being transmitted to the diffuse polarizer by free space20 propagation, a lens system, a light pipe, a polarization preserving light guide, or by other means as are known to the art.
In a fluorescent lamp, such as a hot or cold cathode lamp of the type used in a typical backlit LCD, the light emitting region and the light reflecting, scattering, and depolarizing regions are combined into the phosphors, which se,rve all of these 25 functions. In the case where a highly co1lim~tetl beam of light is desired, the reflective polarizing element can be optically configured to image the rejected polarization back onto the light emitting region, which will typically be a filament or arc. The light emitting region may serve both as the light source and the depolarizing region. Alternately, the light source may comprise a light en-itting 30 region and a separate randomizing reflector.

As described previously, the optical films of the present invention may be either a diffuse reflecting pol~ri7ing film (DRPF), in which light of one plane of polarization is transmitted and light of the other plane of polarization is diffusely reflected, or it may be a diffuse reflecting mirror film (DRMF) in which both planes of polarization are diffusely reflected from the film. As such, the optical film of the present invention may be used in a light fixture as the reflective element and/or the pol~ri7ing el~ment Since the film is diffusely reflective and optically translucent, a separate diffusing element is not necess~ry and the present optical film can function as both the diffusing element and the polarizing element.
o Optical films of the present invention may be used in conventional luminairies that use louvers both to direct the light as well as to obscure the light source from direct view. If films of the present invention are l~minAted or otherwise juxtaposed to conventionally mirrored louvers, then one polarization of light could be diffusely reflected, whereas the second polarization of light could be directed (e.g., nearly vertically) to minimi7~ glare throughout the illumin~ted area.
One could envision the use of at least two pieces of optical film of the present invention, where one is rotatable ~,vith respect to the other, used in lighting fixtures so that the intensity and/or degree of polarized light could be controlled or tuned for the specific needs of the immetli~tP environment.
For those applications where polarized light is not required, such as in the typical hlmin~ires used for office lighting, the light fixture generally consists of a housing co~ it ;~g a light source, such as a fluorescent bulb, a reflecting element behind the light source, and a diffusing element. The source may be any of the light sources noted above (e.g., a fluole3cell~ lamp). The reflecting element may be any reflective surface, inchl-ling, for e~,lple, a painted white reflector, a met~lli7~d film such as Silverlux TM brand reflective film (available commercially from 3M
Company, St. Paul, MN), a reflective metal surface such as polished al-lminllm, or a reflective multilayered, birefringent mirror film such as that described in WO95/17303 and WO 96/19374 and incorporated herein by ,~,f.rellce. In one embodiment, the D~MF of the present film as herein described may be used as the reflective elem~nt in a non-polarized light fixture. The D~MF may additionally be mf~t~ i7.~l either by vapor coating or l~min~tin~ a reflective metal to the back side of the DRMF to improve total reflectivity.
Many applications re~uire polarized light to function properly. Examples of such an applications include optical displays, such as liquid crystal displays 5 (LCDs), which are widely used for lap-top computers, hand-held calculators, digital watches, automobile dashboard displays and the like, and polarized l-lmin~ires and task lighting which make use of polarized light to increase contrast and reduce glare. For applications where polarized light is desired, the light fixture generally consists of a housing cont~ining a light source and a polarizing element, o - and may additionally include a reflecting element and/or a diffusing element. The light source may be any of the light sources described above (e.g., a fluoIesce~lt lamp), but is preferably a diffuse light source which emits light having a high degree of scatter or randomization with respect to both polarization and direction.
The reflecting element, if present, may be any of the reflective materials described above, or may also be the BRMF of the present invention. The polarizing element may include any polarizer, including absorbing dichroic, thin film dielectric orcholesteric polarizers, but is preferrably the multilayer birefringent reflective polarizer described in WO 95/17303 and WO 96/19347.
Absorptive polarizers typically use dichroic dyes which transmit light of one polarization orientation more strongly than the orthogonal polarization orientation. When an absorptive polarizer is used in a display or polarized light fixture, for example, the absorbed light does not contribute to the illumination, and thus to the overall brightn~cs, of the LCD or lunlinaile. The use of such polarizers in li~hting applications is described in U.S. Pat. Nos. 3,124,639 (Kahn), 3,772,128 2s (Kahn), and 4,796,160 (Kahn), and in U.S. Pat. Nos. 5,184,881 (Karpen) and 5,359,498 (Karpen). Vacuum deposited, thin film dielectric polari~rs are not absorbing, as are dichroic polarizers, but do suffer other disadvantages, such as poor angular response and poor spectral tr~n.~mi~ion for non-clesign~l wavelengths. In addition, they are conventionally coated onto stable substrates,such as bulk optical glass or polymer substrates, and this may render them too bulky and heavy for use in lighting applications requiring light weight and small -so-W O 97/32225 PCTrUS97/02995 profile. For some lighting applications, these polarizers may be comhin~l with asuitable light source and the DRMF of the present invention to provide a polarized light fixture.
The preferred reflective polarizers specularly transmit light of a desired ~ s polarization and reflect light of another polarization. Light produced by a diffuse source is randomly polarized and therefore has polarization components (a) and (b) present. This light is incident on the reflective polarizing element. The reflective polarizing element is adapted to transmit light having a first polarization component (polarization component (a) in this example), and reflect light havingo the orthogonal polarization component ((b) in this example). Consequently, light of polarization component (a) is transmitted by the reflective pol~ri7ing element, while light of polarization coll.ponent (b) is reflected back into the light fixture where it is randomized. Some of the initially rejected light is thus converted into the desired polarization and is specularly transmitted through the reflective polarizing element. This process contimlps~ and the repeated reflections and subsequent randomization of light of the undesired polarization increases the amount of light of the desired polarization that is emitted from the diffuse polarized light fixture. The result is a very efficient system for producing light of a desired polarization. The repeated reflections and randomizations effected by the combination of the diffuse source and the reflective polarizing element form an efficient meçh~ni~m for converting light from state (b) to state (a). The system is efficient in the sense that light which would otherwise have been absorbed, and therefore unavailable, is instead converted to the desired polarization. A lightfixture using such a polarizing elçnn~nt thus makes much more efficient use of the light ~mitted from the source, since light of the rejected polarization is reflected back into the source and randomized. As a result, the total amount of light emitted from the fixture in the desired polarization is increased. The use of a multilayer birefringent reflective polarizing film (RPF) in li~htin~ applications is described in applicants commonly ~sign~d U.S. Patent Application Serial Numbers 08t418,009 and 08/479,319, also incorporated herein by reference. These applications describe the use of the multilayer RPF in lighting applications, especially in LCD displays and polarized lnmin~ires. The reflective polarizing element of these applications transmits light of a desired polarization and specularlY reflects light of another polarization back into the diffuse source where it is randomized. When a multilayer RPF is used in this way, a sep~udle diffuser film is typically used in lnmin~ires or s t~k li~htine applications so that the light source is not dir~,~,lly visible. A
reflective element is preferably also included in these polarized light fixtures, and the reflective element may comprise the BRMF of the present invention or any other suitable reflective surface that either r~n(lomi7~s the light reflected from the RPF or reflects the reflected light back into a diffusing source where it can be0 randomized and partially converted into the correct polarization to be tr~n~mitt~l by the pol~ri~ine elem~nt The DRPF of the present invention functions similar to the multilayer RPF
to increase the amount of light of the desired polarization that is emitted by the polarized light fixture, however, the initially rejected light of the wrong 15 polarization is diffuselv reflected back into the light fixture where it may be randomized, partially converted to light of the correct polarization, and specularly transmitted through the polarizing element. The diffuse reflective polarizing film (DRPF) of the present invention is translucent so that a separate diffuser is not neecle~ When combined with the light source to make a diffuse reflecting 20 polarized light fixture, a reflecting element is preferably also included to direct the reflected light back to the source and/or aid in the randomization and partial conversion of the reflected light into light of the correct polarization to be transmitted by the polarizing element. The reflecting element may be any suitable reflective m~t~ri~l, as described above, and in particular may be the DRMF of the 25 present invention. As such, the DRMF of the present invention may be used in one embodiment as the reflecting element and the DRPF of the present invention may be used as the polarizing element and/or the diffusing element.
In the light fl~ s described herein, the light source may be coupled with the polarizing element and reflecting element in a variety of configurations. Some 30 of the configurations will be described with respect to using the diffuse reflecting pol~r?~ine film (DRPF) of the present invention as the polarizing element and the diffuse reflecting mirror film (DRMF) of the present invention as the reflectingel~ment but it should be recognized that various combinations of DRPF with othermaterials as the reflecting element and DRMF with other materials as the polarizing element are envisioned. In one configuration, the DRPF may be s wrapped around such that it completely encloses the diffuse source. A separatereflector may be used in addition to the light source and DRPF. The reflector may be a diffuse reflective film (DRMF) which randomizes the light of polarization (b) that is reflected from the DRPF, or it may be a specular reflector which redirects light to the light emitting region of a diffuse randomizing light source. The DRMF
o may be oriented around one side of the light source and may be l~min~ted or otherwise ~ ch~ocl to the light source. In this configuration, the DRPF may also be l~min~ted or otherwise ~tt~- ~. .l so that it partially encloses the other side of the light source.
The embo~lim~nt~ of the present polarized light source using the DRPF
15 have several advantages. The reflection and randomization process achieved with the light source and DRPF gives a polarized light fixture that is very efficient. The bro~tlb~ntl reflectivity provided by the DRPF means that efficiency is achieved over a broad spectral range. In addition, the DRPF provides high off-angle reflectivity of the rejected polarization. These features make the DRPF/diffuse 20 source combination useful over a broader range of the optical spectrum and over a broader range of angles than the embo-iimPnt~ incoll,ol~ling bulk optic components. In addition, the DRPF is lightweight, thin and flexible, which makesit good for applications requiring low bulk and light weight. The DRPF also conforms well to the lamp surface and could be incorporated into the lamp 25 m~m-f~r,ture. Furthermore, since the DRPF is a diffuse reflector, its opaque a~ea~ance obviates the need for a s~p~ale diffuser film that is typically used in polarized l~llhlail~s and task liphting fixtures to obscure the light source from direct viewing.
In yet another application, optical films of the present invention may be 30 used to generate polarized light used in smoke detection systems or in the analysis of the polarization of light scattered from smoke particles, including those smoke detection systems which alL~ t to define the nature or origin of the combustion as taught by U.S. 5,576,697 (N~g~chim~ et al.).

Light Extractors sThe optical films of the present invention may be used as light extractors in various optical devices, including light guides such as the Large Core Optical Fiber (LCOF) illustrated in ~IG. 8. The LCOF 50 uses very efficient total intern~l reflection (TIR) to guide light substantial ~ t~nces from an illllmin~tQr or light source 52. However, when the optical films of the present invention are applied as lo an e~tern~l cl~ ling 54, they upset the light guiding at the fiber-to-air interface, thereby ejecting light out into the surrolln-ling.c This feature may be used advantageously in various remote source lighting applications, such as architectural highlighting, decorative lighting, medical lighting, signage, visual guidance (e.g., on l~n~ling strips or in aisles for airplanes or theatres), display (e.g., instrument 5 displays, especi~lly those in which excessive heating is a problem) and exhibit lighting, roadway lightinE, automotive lighting, downlighting~ task lighting, accent lighting, and ambient lighting. ln some applications, the films of the present invention may be applied as a cJ~lriing at multiple locations along the length of the fiber, thereby illl.min~ting multiple locations from a single light source.
20 Furtherrnore, since these systems are commonly equipped with UV and IR filters, the lighting produced by such systems will not degrade UV sensitive materials, nor will the light guides heat up with use.
The films of the present invention can also be made to extract only a single polarization of light, thereby creating a polarization-specific source., With proper 25 configuration of the light fiber system, substantially all of the light injected into the fiber will eventually make its way through the extractor in the desired polarization.
Polarization-specific sources can be made, for example, by using an optical film of the present invention which is a strong diffuse scatterer for light of a first polarization, but is a non-scattering, specular material which m~int~in.c a total 30 intern~l reflection (TIR) cladding-to-surface interface for light of a second polarization. Such a system is described in Example 134.

Suitable light guides for use in the present invention include both side emitting and end emitting fibers. The light guides themselves may be glass or plastic and may be of varying diameters, depending on such factors as the required efficiency at collecting light, required flexibility, and whether the light guides are to be used alone or in bundles. The light guides may also be fiber optic light guides or prism light guides, with the later being more suitable for large scaleapplications, and the former being more suitable for smaller scale applications where cost per lumen is less hlllJu~
Commercially available light guides that are suitable for use in the present o invention include those made from films of low Tg acrylic polymers, such as the optical lighting film available colll~n~;cially from 3M under the tr~den~me Scotch Optical T.iFhting Film (SOLF). Such film, which acts like a mirror towards lightstriking it at certain angles, is a ~ s~ent plastic film which has a pri~m~tiC
surface (typically microreplicated) on one side and a smooth surface on the other.
The film is commonly used in conjunction with a tubing or backing of a spale.l~ or opaque plastic or metal. Other suitable light guides include the linear ill--min~tion fiber optics available commercially from Lumenyte under thetr~clen~me FiberescentTM, and the end-emitting fibers available commercially from Fiberstars under the tr~ n~me FiberSpotsTM.
Various light sources may be used in conjunction with the light guides made in accordance with the present invention, depending on the application to which the light guide is directed. Such sources are described, for example, in T i,~htin~ Futures, Vol. 1, No. 3 (1995), a publication of the T ighting Research Center, Rensselaer Polytechnic Tnetit~lte, Troy, N.Y. Typically, a low voltage 20-75 watt MR16 lamp used in conjunction with a fiber optic system will be suitablefor applications such as m~lce~ m, display and accent li~hting, while a 70-250 watt metal halide lamp, used in conjunction with a fiber optic or prism light guide system, is suitable for applications such as architectural or outdoor li~hting applications. For applications requiring 250 watts or greater, metal halide or high pressure sodium lamps may be used in conjunction with prism light guide systems Other suitable light sources include 60 watt xenon metal halide lamps, -5s-commercially available from General Electric Company, Danbury, Connecticut, which are particularly useful for automotive applications, and sulfur lamps, commercially available from Fusion r iphtin~, Rockville, MD, which have been used successfully on an experim~nt~l basis in prism light guide systems. Compactand tubular fluoresce,l~ lamps may also be used where a larger diffuse light source is neecle(l Sunlight may also be used with fiber optic or prism light guide systems, and in conjunction with mirrors or lenses, as part of a s~nlight harvesting system.
In some bacl~liEht display devices, such as those used in avionics applications where high levels of ambient light impinge on the front surface of the o device, high intensities rA.~liAtinE from the display are required to provide sufficient contrast to the display. Consequently, excessive heating of the backlight assembly in such systems can occur unless means are provided to dissipate the unwanted heat. A variety of means are used in the art to eliminAte the heat, such as the use of cold mirrors and filters and other means.
s In most new aircraft, ambient sunlight potentially reduces contrast to the flat panel displays used, and spatial ~e~luh~llents for the ensemble of displays are critical desgin parameters. Thel~fole, in one form of the present invention, light is transported to the display(s) via fiber optics from a remotely located, but int~nce source, where the latter can be cooled efficiently and the undesired heat not affect the operation of the display device. Since these displays typically work on the basis of polarized light propAEAtinE through a liquid crystal display, the optical films of the present invention may be used in such systems as light extractors of substantially one polarization. The second polarization would continue to reflect inside the optical fiber until its polarization is converted to the first polarization 2s and can be emitted from the light extractor at the places where the light is n~ecle~l Overview of Examples The following Examples illustrate the production of various optical materials in accordance with the present invention, as well as the spectral ~;rop~llies ofthese mAteriAI~. Unless otherwise indicated, percent composition refers to percent composition by weight. The polyethylene nAphthAlAte resin used -s6-W O 97/32225 PCTrUS97/02995 was produced for these samples using ethylene glycol and dimethyl-2,6-n~phth~lenedicarboxylate, available from Amoco Corp., Chicago, Illinois. These reagents were polymerized to various intrinsic viscosities (IV) using conventional polyester resin polymerization techniques. Syndiotactic polystyrene (sPS) may beproduced in accordance with the method disclosed in U. S. Patent 4,680,353 (Ishihara et al). The examples includes various polymer pairs, various fractions of continuous and disperse phases and other additives or process changes as discussed below.
Stretching or orienting of the samples was provided using either o conventional orientation equi~l~lclll used for m~king polyester film or a laboratory batch orienter. The laboratory batch orienter used was ~leci~n~rl to use a small piece of cast material (7.5cm by 7.5cm) cut from the extruded cast web and held by a square array of 24 ~I;~C-s (6 on each side). The orientation telllp~,ldlllle of the sample was controlled a hot air blower and the film sample was oriented through a mechanical system that increased the ~lict~nl e between the ~ p~l~ in one or both directions at a controlled rate. Samples stretched in both directions could be oriented sequentially or simultaneously. For samples that were oriented in the constrained mode (C), all ~,I;pp~.~ hold the web and the g~;pi)els move only in one dimension. Whereas, in the unconstrained mode (U), the gl;ppCl~ that hold the film at a fixed tlim~ncion perpendicular to the direction of stretch are not engaged and the film is allowed to relax or neckdown in that ~lim~ncjon.
Polarized diffuse tr~ncmi.ccion and reflection were measured using a Perkin Elmer Lambda 19 ultraviolet/visible/near infrared spectrophotometer equipped with a Perkin Elmer Labsphere S900-1000 150 millimeter integrating sphere accessor,v and a Glan-Thompson cube polarizer. Parallel and crossed tr~ncmiccionand reflection values were measured with the e-vector of the polarized light parallel or perpendicular, respectively, to the stretch direction of the film. All scans were continuous and were con~ cte-l with a scan rate of 480 nanometers per minute anda slit width of 2 nanometers. Reflection was pclro~llled in the "V-reflection"
mode. Tr~ncmic,cion and reflectance values are averages of all wavelengths from 400 to 700 n~nl meters.

Tr~n~miesion electron micrographs were taken of fini~hed film, cross-sectioned in a plan perpendicular to the m~rhine direction to determine the nature of the dispersed phase. The outer layers of three-layer constructions were removed from oriented film, leaving only the blend layer for embedding. Samples were 5 embedded in 3M ScotchcastTM 5 Electrical Resin which was cured at room t~ ,c.dL lre. The embedded samples were microtomed using a diamond knife, on a Reichert UltracutTM S microtome at room temperature, into thin sections of approximately 90nm thickness, using a cuning rate of 0.2 millimeters per second.The thin sections were floated onto ~ tille~1, deionized water and collected for0 tr~n.~mi~ion electron microscopic evaluation on a 200 mesh copper grid relforced with a carbon/forrnvor substrate. Photomicrographs were taken using a JEOL
200CX Tr~n~micsion Electron Microscope.
Sç~nning electron microscopic evaluations were p~lrolmed on cast webs prior to film orientation to (1et~rmine the nature of the disperse phase. Pieces of web were fractured to expose a plane perpendicular to the m~hin~ direction whileed in liquid nitrogen. Samples were then trimmed and mounted on alurninum stubs prior to sputter coating with gold palladium. Photomicrographs were taken using a Hitachi S530 Sc~nnin~ Electron Microscope.

In Example 1, an optical film was made in accordance with the invention by extruding a blend of 75% polyethylene n~phth~l~te (PEN) as the continuous or major phase and 25% of polymethylmeth~crylate (PMMA) as the disperse or minor phase into a cast film or sheet about 380 microns thick using conventional extrusion and casting techniques. The PEN had an intrinsic viscosity (IV) of 0.52 (measured in 60% phenol, 40% dichlorobenzene). The PMMA was obtained from ICI Americas, Inc., Wilmington, Delaware, under the product clecign~tion CP82.
The extruder used was a 3.15 cm (1.24") Brabender with a 1 tube 60 llm Tegra filter. The die was a 30.4 cm (12") EDI UltraflexTM 40.
About 24 hours after the film was extruded, the cast film was oriented in the width or transverse direction (TD) on a polyester film ~ device. The W O 97/32225 PCTrUS97/02995 stretching was accomplished at about 9.1 meters per minute (30 ft/min) with an output width of about 140 cm (55 inches) and a stretching te~ JeldLu~e of about 160~C (320~F). The total reflectivity of the stretched sample was measured with an i..Le~,~dling sphere att~rllment on a Lambda 19 spectrophotometer with the sample beam polarized with a Glan-Thompson cube polarizer. The sample had a 75% parallel reflectivity (i.e., reflectivity was measured with the stretch direction of the film parallel to the e-vector of the polarized light), and 52% crossed reflectivity (i.e., reflectivity was measured with the e-vector of the polarized light perpendicular to the stretch direction).

In Example 2, an optical film was made and evaluated in a manner similar to Example 1 except using a blend of 75% PEN, 25% syndiotactic polystyrene (sPS),0.2% of a polystyrene glycidyl methacrylate compatibilizer, and 0.25% eachof IrganoxTM 1010 and UltranoxTM 626. The synthesis of polystyrene glycidyl methacrylate is described in Polymer Processes, "Ch~rnic~l Technology of Plastics, Resins, Rubbers, Adhesives and Fibers", Vol. 10, Chap.3, pp.69-109 (1956)(Ed.
by Calvin E. Schil-lkn~.~ht).
The PEN had an intrinsic viscosity of 0.52 measured in 60% phenol,40%
dichlorobenzene. The sPS was obtained from Dow Chemical Co. and had a weight average molecular weight of about 200,000, design~ted subsequently as sPS-200-0.The parallel reflectivity on the stretched film sample was ~iet~rmin~d to be 73.3%, and the crossed reflectivity was detçrminpcl to be 35~/O.

2s EXAMPLE 3 In Example 3, an optical film was made and evaluated in a manner similar to Example 2 except the compatibilizer level was raised to 0.6%. The resulting parallel reflectivity was detçl~nined to be 81% and the crossed reflectivity wasdel~ ed to be 35.6%.

_59_ In Example 4, an three layer optical film was made in accordance with the present invention ~ltili7ing conventional three layer coextrusion techniques. The film had a core layer and a skin layer on each side of the core layer. The core layer consisted of a blend of 75% PEN and 25% sPS 200-4 (the ~lçcign~tion sPS-200-4 refers to a copolymer of syndiotactic-polystyrene co~ it~g 4 mole % of para-methyl styrene), and each skin layer con~i~tecl of 100% PEN having an intrinsic viscosity of 0.56 measured in 60% phenol, 40% dichloroben7~n~
The resulting three-layer cast film had a core layer thickness of about 415 microns, and each skin layer was about 110 microns thick for a total thickness of about 635 microns. A laboratory batch stretcher was used to stretch the resulting three-layer cast film about 6 to 1 in the m~hinP direction (MD) at a tell~pcildlule of about 129~C. Because the edges ofthe film sample parallel to the stretch direction were not gripped by the lab stretcher, the sample was unconstrained in the transverse direction (TD) and the sample necked-down in the TD about 50% as a result of the stretch procedure.
Optical perfo.l..~lce was evaluated in a manner similar to Example l. The parallel reflectivity was determined to be 80.1%, and the crossed reflectivity was det~rmined to be 15%. These results demonstrate that the film performs as a low 20 absorbing, energy conserving system.

In Examples 5-29, a series of optical films were produced and evaluated in a manner similar to Exarnple 4, except the sPS fraction in the core layer and the IV
2s of the PEN resin used were varied as shown in Table 1. The IV of the PEN resin in the core layer and that in the skin layers was the same for a given sarnple. Thetotal thickness of the cast sheet was about 625 microns with about two-thirds ofthis total in the core layer and the balance in the skin layers which were a~p~ ately equal in thickness. Various blends of PEN and sPS in the core layer 30 were produced, as indicated in Table 1. The films were stretched to a stretch ratio of about 6:1 in either the m~ ine direction (MD) or in the transverse direction WO 97/32225 PCTtUS97/02995 (TD) at various te~ alules as indicated in Table 1. Some of the samples were con~l dined (C) in the direction perpendicular to the sketch direction to prevent the sample from nçc1~ing down during ~lletcl~ g The samples labeled "U" in Table 1 were unconstrained and p.,lllliLI~d to neckdown in the unconstrained Aimen~ion.
5 Certain optical properties of the sketched samples, including percent k~n~mi~sion, reflection, and absorption, were measured along axes both parallel and crossed or perpendicular to the direction of stretch. The results are summarized in TABLE 1.
Heat setting, as indicated for E~nples 24-27, was accomplished by m~nll~lly con:~llailling the two edges of the sketched sample which were 10 perpendicular to the direction of sketch by clamping to an applol,llately sized rigid frame and placing the cl~mped sample in an oven at the in-lic~tecl l~lllp.,.dlure for 1 minute. The two sides of the sample parallel to the direction of stretch were unconstrained (U) or not clamped and allowed to neckdown. The heatsetting of F~mrle 29 was similar except all four of the edges of the stretched sample were IS conslldilled (C) or clamped. Example 28 was not heat set.

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~3 W ~ 97/32225 PCT~US97/02995 All of the above samples were observed to contain varying shapes of the disperse phase depending on the location of the disperse phase within the body of the film sample. The disperse phase inclusions located nearer the surfaces of the samples were observed to be of an elongated shape rather than more nearly s spherical. The inclusions which are more nearly centered between the surfaces of the samples may be more nearly spherical. This is true even for the samples withthe skin layers, but the magnitude of the effect is reduced with the skin layers. The addition of the skin layers improves the processin~ of the films by reducing theten~ency for splitting during the stretching operation.
Without wishing to be bound by theory, the elongation of the inclusions (disperse phase) in the core layer of the cast film is thought to be the result of shear on the blend as it is transported through the die. This elongation feature may be altered by varying physical flim~ncions of the die, extrusion temp~rdlul~, flow rate of the extrudate, as well as chemical aspects of the continuous and disperse phase materials which would alter their relative melt viscosities. Certain applications or uses may benefit from providing some elongation to the disperse phase during extrusion. For those applications which are subsequently stretched in the m~chine direction, starting with a disperse phase elongated during extrusion may allow ahigher aspect ratio to be reached in the resulting disperse phase.
Another notable feature is the fact that a noticeable improvement in performance is observed when the same sample is stretched uncol~ dilled. Thus, in Example 9, the % tr~ncmi~sion was 79.5% and 20.3% in the parallel and perpendicular directions, lesl~e~ ely. By contrast, the tr~ncmiCcion in Flt~mple16 was only 75.8% and 28.7% in the parallel and perpendicular directions, respectively. There is a thickness increase relative to constrained ~le~ching when sarnples are stretched nnconetrained, but since both tr~ncmic.cion and extinction improve, the index match is probably being improved.
An alternative way to provide refractive index control is to modify the chemictry of the materials. For example, a copolymer of 30 wt % of interpolymeri7Pd units derived from terephthalic acid and 70 wt % of units derived from 2,6~ h~lic acid has a refractive index 0.02 units lower than a 100% PEN

W O 97132225 PCT~US97102995 polymer. Other monomers or ratios may have slightly different results. This typeof change may be used to more closely match the refractive indices in one axis while only c~ ing a slight reduction in the axis which desires a large difference.
In other words, the benefits ~tt~ined by more closely m~tçhing the index values in 5 one axis more than compensate for the reduction in an orthogonal axis in which a large difference is desired. Secondly, a chemical change may be desirable to alter the te,l.p~l~L lre range in which stretching occurs. A copolymer of sPS and varying ratios of para methyl styrene monomer will alter the optimum stretch-temperaturerange. A combination of these techniques may be necess~. y to most effectively 0 optimize the total system forprocessing and res--lting refractive index m~tc~es and differences. Thus, an improved control of the final performance may be ~ inf ~l by optimi7ing the process and ch~mictry in terms of stretching conditions and further adjusting the cl-~mi~try ofthe m~teri~lc to maximize the dirr~,lence in refractive index in at least one axis and minimi7ing the difference at least one15 orthogonal axis.
These samples displayed better optical performance if oriented in the MD
rather than TD direction (compare Examples 14-15). Without wishing to be bound by theory, it is believed that different geometry inclusions are developed with an MD orientation than with a TD orientation and that these inclusions have higher 20 aspect ratios, m~king non-ideal end effects less important. The non-ideal endeffects refers to the complex geometry/index of refraction relationship at the tip of each end of the elongated particles. The interior or non-end of the particles are thought to have a ullirolln geometry and refractive index which is thought to bedesirable. Thus, the higher the ~lcentage of the elongated particle that is uniform, 25 the better the optical perforrnance.
The extinction ratio of these m~teri~ls is the ratio of the tr~n~mi~ion for polarizations perpendicular to the stretch direction to that parallel to the stretch direction. For the examples cited in Table 1, the extinction ratio ranges between about 2 and about 5, although extinction ratios up to 7 have been observed in 30 optical bodies made in accordance with the present invention without any attempt to optimize the extinction ratio. It is expected that even higher extinction ratios -6s -W O 97t32225 PCTrUS97/02995 (e.g., greater than 100) can be achieved by adjusting film thickness, inclusion volume fraction, particle size, and the degree of index match and mi~m~tch, or through the use of iodine or other dyes.

s EXAMPLES 30-100 In Examples 30-100, samples ofthe invention were made using various materials as listed in Table 2. PEN 42, PEN 47, PEN 53, PEN 56, and PEN 60 refer to polyethylene ll~pli~ te having an intrinsic viscosity (IV) of 0.42, 0.47, 0.53, 0.56, and 0.60, l~s~e~ ely, measured in 60% phenol, 40% dichlorob~r.,f l-e.
Io The particular sPS-200-4 used was obtained from Dow Chemical Co. EcdelTM
9967 and EastarTM are copolyesters which are available coll.mercially from F~tm~n Chemical Co., Rochester, New York. SurlynTM 1706 is an ionomer resin available from E.I. du Pont de Nemours & Co., Wilmington, Delaware. The materials listed as Additive 1 or 2 include polystyrene glycidyl methacrylate. The dP~ign~tions GMAPS2, GMAPS5, and GMAPS8 refer to glycidyl methacrylate having 2, 5, and 8% by weight, respectively, of glycidyl methacrylate in the total copolymer. ETPB refers to the crosslinking agent ethyltriphenylphosphonium bromide. PMMA V044 refers to a polymethylmethacrylate available commercially from Atohaas North America, Inc.
The optical film samples were produced in a manner similar to Example 4 except for the differences noted in Table 2 and ~ c~ e(l below. The continuous phase and its ratio of the total is reported as major phase. The disperse phase and its ratio of the total is reported as minor phase. The value reported for blend thickness leplesel-l~ the approximate thickness of the core layer in r¢licrons. The 2s thickness of the skin layers varied when the core layer thickness varied, but was kept to a constant ratio, i.e., the skin layers were approximately equal and the total of the two skin layers was about one-third of the total thickness. The size of the disperse phase was ~ieterrnin~cl for some samples by either sc~l".ing electron microscope (SEM) or IlA~ ion electron microscope (TEM). Those examples which were subsequently stretched using the laboratory batch orienter are shown by an "X" in the column labeled Batch SLI~tchcd.

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W O 97/32225 PCTrUS97/~2995 The presence of the various compatibilizers was found to reduce the size of the included or disperse phase.

In Example 101, an optical film was made in a manner similar to Example 4 except the resulting core thickness was about 420 microns thick, and each skinlayer was about 105 microns thick. The PEN had a 0.56 IV. The cast film was oriented as in Example 1, except the temperature of stretch was 165~C and there o was a 15 day delay between casting and stretching. The tr~n~mi~ion was 87.1%
and 39.7% for parallel and perpendicularly polarized light, respectively.

In Examples 102 - 121, optical films were made as in Example 101, except that orientation conditions were varied and/or the sPS-200-0 was replaced with either copolymers of sPS cont~ining either 4 or 8 mole % of para-methyl styrene or with an atactic-form of styrene, Styron 663 (available from Dow Chemical Company, Midland, Michigan) as listed in Table 3. Evaluations of tr~n~mi~sion properties are also reported. Tr~n~mi~ion values are averaged over all wavelengths between 450-700 nm.

W O 97t32225 PCT~US97/02995 Ex.% PS PEN Temperature Rail Perpendicular Parallel sPS IV of DrawSetting Tr~n~mi~ion Transmission (~C) (cm) (%) (%) 101 25 200-0 0.56 165 152 87.1 39.7 102 35 200-0 0.56 165 152 87.8 44.4 103 15 200-4 0.56 165 152 86.1 43.5 104 25 200-4 0.56 165 152 86.5 43.6 105 35 200-4 0.56 165 152 88.2 50.7 106 15 200-8 0.56 165 152 89.3 40.7 107 25 200-8 0.56 165 152 88.5 42.8 108 35 200-8 0.56 165 152 88.6 43.3 109 15 Styron 0.56 165 152 89.3 45.7 110 25 Styron 0.56 165 152 87.8 41.6 111 35 Styron 0.56 165 152 88.8 48.2 112 15 Styron 0.48 165 152 88.5 62.8 113 25 Styron 0.48 165 152 87.1 59.6 114 35 Styron 0.48 165 152 86.8 59.6 115 15 200-0 0.48 165 152 88.0 58.3 116 25 200-0 0.48 165 152 88.0 58.7 117 35 200-0 0.48 165 152 88.5 60.6 118 l S 200-4 0.48 165 152 89.0 57.4 119 35 200-4 0.48 165 152 87.3 64.0 120 35 200-0 0.56 171 127 86.5 65.1 W O 97132225 PCTrUS97/02995 Ex. % PSPEN Te~ ,.dl~reRail Perpendicular Parallel sPS IV of DrawSetting Tr~n~mi~ion Transmission (~C) (cm) (%) (%) 121 35200-00.56 171 152 88.1 61.5 These examples indicate that the particles of the included phase are elongated more in the m~rhine direction in high IV PEN than in low IV PEN. This is con~i~tt?nt with the observation that, in low IV PEN, stretching occurs to a greater extent near the surface of the film than at points interior to the film, with the result that fibrillar structures are formed near the surface and spherical structures are formed towards the center.
Some of these Examples suggest that the orientation temperatures and degree of orientation are important variables in achieving the desired effect.
o Exarnples 109 to 114 suggest that quiescent cryst~lli7~tion need not be the only reason for the lack of tr~n.~mi~ion of a plerell~d polarization of light.

In Example 122, a multilayer optical film was made in accordance with the invention by means of a 209 layer feedblock. The feedblock was fed with two materials: (1) PEN at 38.6 kg per hour (intrinsic viscosity of 0.48); and (2) a blend of 95% coPEN and 5% by weight of sPS homopolymer (200,000 molecular weight). The coPEN was a copolymer based on 70 mole % n~phth~lene dicarboxylate and 30 mole % dimethyl isophth~l~te polymeri7.~-1 with ethylene glycol to an intrinsic viscosity of 0.59. The coPEN/sPS blend was fed into the feedblock at a rate of 34.1 kg per hour.
The coPEN blend material was on the outside of the extrudate, and the layer composition of the resulting stack of layers ~ltçrn~te~ between the two materials. The thickn~s~es of the layers was designed to result in a one-quarter- 2s wavelength stack with a linear gradient of thicknesses, and having a 1.3 ratio from the thinn~ct to the thickest layer. Then, a thicker skin layer of coPEN (made inaccordance with the method described above to make the coPEN/sPS blend, except the molar ratios were 70/15/15 naphthalene dicarboxylate /dimethyl terephth~l~te/dimethyl isophth~lAte) devoid of sPS was added to each side of the209 layer composite. The total skin layer was added at a rate of 29.5 kg per hour, with about one-half of this quantity on each side or surface of the stack.
The resulting skin layer clad multilayer composite was extruded through a multiplier to achieve a multilayer composite of 421 layers. The resulting multilayer composite was then clad with another skin layer of the 70/15/15 coPENon each surface at a total rate of 29.5 kg per hour with about one-half of this quantity on each side. Since this second skin layer may not be separately o detectable from the existing skin layer (as the material is the sarne), for the purposes of this discussion, the resulting extra thick skin layer will be counted as only one layer.
The resulting 421 layer composite was again extruded through a 1.40 ratio asymrnetric multiplier to achieve a 841 layer film which was then cast into a sheet s by extruding through a die and quPn~hing into a sheet about 30 mils thick. The resulting cast sheet was then oriented in the width direction using a conventional film m~kin~ tentering device. The sheet was stretched at a temperature of about 300~F (149~C) to a stretch ratio of about 6: 1 and at a stretch rate of about 20% per second. The resulting stretched film was about 5 mils thick.
In Exarnple 123, a multilayer optical film was made as in Example 122, except that the amount of sPS in the coPEN/sPS blend was 20% instead of 5%.
In Example 124, a multilayer optical film was made as in Example 122, except that no sPS was added to the film.
The results reported in Table 4 include a measure of the optical gain of the film. The optical gain of a film is the ratio of light transmitted through an LCD
panel from a bAcklight with the film inserted between the two to the light transmitted without the film in place. The significance of optical gain in the context of optical films is described in WO 95/17692 in relation to Figure 2 of that reference. A higher gain value is generally desirable. The trAn~mi~sion values include values obtained when the light source was polarized parallel to the stretch direction (Tl) and light polarized perpendicular to the stretch direction (Tl). Off-W O 97/32225 PCTrUS97/02995 angle-color (OAC) was measured using an Oriel spectrophotometer as the root mean square deviation of p-polarized tr~n~mi~sion at 50 degree incident light ofwavelength between 400 and 700 nm.

Ex.mole % sPS Gain Tl (%) Tll (%) OAC (%) 122 5 1.5 83 2 1.5 123 20 1.45 81 1.5 1.2 124 0 1.6 87 5 3.5 The value of off-angle-color (OAC) demonstrates the advantage of using a multilayer construction within the context of the present invention. In particular, 0 such a construction can be used to substantially reduce OAC with only a modestreduction in gain. This tradeoffmay have advantages in some applications. The values of Tll for the examples of the invention may be lower than expected because light scattered by the sPS dispersed phase may not be received by the detector.

A three layer film was made in accordance with Example 4. The core layer consisted of 70% coPEN whose intrinsic viscosity was 0.55 measured in 60%
phenol, 40% dichlorobenzene, 70% sPS 200-7, plus an additional 2% Dylark 332-80 (available from NOVA Chemical). Each skin consisted of 100% coPET having 20 an intrinsic viscosity of 0.65 measured in methylene chloride.
The coPEN was a copolymer based on 62 mole % n~phth~lene dicarboxylate and 38 mole % dimethyl terephth~l~te. The coPET was a copolymer based on 80 mole % dimethyl carboxylate and 20 mole % dimethyl isophth~l~te.
The cast film was oriented in a manner con.ci~tent with Example 1. The 25 stretching was accomplished at 5.8 meters per minute (19 feet per minute) with an output width of 147 cm (58 inches). The stretch temperature was 124~C. The heat set te,llpelal lre was 163~C. The perpendicular tr~n.~mi.~ion was 85.3%, and the parallel tr~n~mi~cion was 21.7%.

W O 97/32225 PCTrUS97/02995 The following examples illustrate the production of a co-continuous morphology in an optical system of the present invention.
s In Examples 126 through 130, a series of optical films were produced and evaluated in a manner similar to Examp}e 125, except the sPS fraction in the core layer and the stretch temperature were varied as shown in Table 5.

Example Fraction Dispersed Stretch Trans. Trans.
Number sPS or Co- Temperature (Perp.) (Para.) continuous (~C) 125 0.30 D 124 85.3 21.7 126 0.35 D 135 86.3 21.1 127 0.40 D 129 86.4 21.9 128 0.44 -- 124 85.8 25.9 129 0.53 C 129 86.6 33.6 130 0.81 D 135 88.1 69 The parallel and perpendicular tr~n~mi~sion values for Examples 125 to 130 show good optical p~lro~ ance. The high value for perpendicular tr~n.~mi~ion for Example 130 tr~n~mi~ion suggests an effective match in the refractive indices in both phases for polarized light aligned in the direction 15 perpendicular to the stretch direction.
Sc~nnin~ electron micrographs were taken of fracture surfaces of cast web for Examples 126 and 127. As in Example 125, there was clear evidence of spherical or elliptical particles dispersed in an otherwise continuous matrix.
Tr~n.cmi~sion electron micrographs were taken for Examples 129 and 130; these 20 are shown in Figs. 6a and 6b, respectively. Fig. 6a illustrates the morphology of co-continuous phases. Inspection of the micrograph shows inclusions of both the coPEN and the sPS phases, as well as regions where each appears to be the continuous phase. By contrast, Fig. 6b shows coPEN dispersed into an sPS matrix.

A three layer film was made in accordance with Example 4. The core layer consisted of 85% coPEN whose instrinsic viscosity was 0.51 measured in a s solution of 60% phenol and 40% dichlorobenzene, and 15% 250k-7, plus an additional 2% DylarkTM 332-80. Each skin consisted of 100% coPEN.
The coPEN used as part of the core was a copolymer based on 70 mole %
n~rhth~lene dicarboxylate and 30 mole % dimethyl terephth~l~te. The coPEN
used in the skin layers was a copolymer based on 70 mole % naphthalene dicarboxylate and 30 mole % dimethyl isophth~l~te.
The cast film was oriented in a manner consistent with Example 1. The ~Lletchillg was accomplished at 5.3 meters per minute (17.4 feet per minute) with an output width of 124.5 cm (49 inches). The stretch t~ cldLule was 118~C. The heat set temperature was 141~C. The perpendicular tr~n.cmiccion was 81.9%, and the parallel tr~ncmiccion was 32.7%. The perpendicular tr~ncmiccion spectrum is presented in Figure 7.

A film with an antireflection layer was prepared by first adding 10 grams of RemetTM SP-30 (Remet Coporation, Chadwicks, NY) with 1 gram TritoxTM X-100 (Rohm and Haas, Phil~-lelphi~, PA) into 89 grams of deionized water. The solution was coated onto a piece of film from Example 131 lltili~inE a #3 wire wound rod to yield a dry coating thickness of approximately 200 nanometers. The perpendicular tr~ncmicsion was 83.8%, and the parallel tr~ncmiccion was 33.3%.

- Example 131 was repeated, except that both sides of the film were coated with an antireflection layer. The perpendicular tr~ncmicsion was 86.2%, and the parallel L~ . Iiccion was 33.8%.
The perpendicular tr~ncmicsion spectra for Examples 131 - 133 are presented in Fig. 7. One can see from Fig. 7 that the overall slope of the perpendicular W O 97/32225 PCT~US97/02995 tr~n~mi~ion as a function of wavelength is lower for Examples 13~- 133 relative to Example 131, particularly for the range of wavelength from. One skilled in the art will appreciate that a film exhibiting a flat tr~n~mi~ion curve as a function of the wavelength of light will minimi7e any changes in color to a resultant display s device into which the reflective polarizer might be incorporated.

These examples illustrates the use of the films of the present invention as high efficiency light extractors for light guiding structures.
o In Example 134, an optical film was made in accordance with the present invention by extruding a composition consisting of 30% sPS in a matrix of 70/30/0 coPEN. The extruded film was oriented in the m~rhine direction to a stretch ratio of 2.5:1.
ln Example 135, a second film was made from the same composition as Example 134 and using a similar procedure. However, instead of orienting the film in the m~hine direction, the film was oriented uniaxially in the direction transverse to the m~hinP direction using a tenter stretch of 4.8: 1.
The films of Examples 134 and 135 were mechanically fastened as cladding to separate optical fibers, using a silica grease to elimin~te the fiber-air interface.
The ex~ ent~l set-up is depicted sc.hem~tically in FIG. 8. The fibers were then connected to a 60 watt xenon metal halide short arc lamp obtained from General Electric Company, Danbury, CT. The optical fibers had a thickness of 1.2 cm and con~i~te-l of a low Tg acrylic polymer.
When the lamp was turned on, the two samples became ill--min~tPd and produced diffusely scattered light. When the two film samples were viewed through a polarizing film at an orientation perpendicular to one plane of polarization, both samples a~yealed s~-bst~n~ y darkened. However, when the polarizing film was rotated 90~ in the sa ne plane, both samples aplJealed diffusely bright, indicating that the tr~n~mi.e.cion of light through the films was polarization specific.

W O 97/32225 PCTrUS97/02995 The effect of capping the ends of the fibers was also investig~te~ When the ends were reflectively capped so that a portion of the light escaping from the ends of the fibers was reflected back into the fibers, the intensity of light produced by the films increased. This is con~i~tt-nt with the creation of a light cavity in s which light of the non-extracted polarization undergoes further reflections within the optical fiber until it is converted, by degrees, into the extracted polarization.
With the light within the fiber being unable to exit the fiber except through the extractor, the extraction efficiency increased. In addition, polarization conversion of the light interacting with the fiber/air interface caused a greater portion of light o to be extracted from the fiber in the desired polarization.

The following example illustrates the increase in gain achievable at non-normal incident angles with the optical films of the present invention.
s A three layer film was made in accordance with Example 4. The core layer consisted of 70~/O PEN whose instrinsic viscosity was 0.48 (measured in 60%
phenol, 40% dichlorobenzene) and 30% sPS 200-8. Each skin consisted of 100%
coPEN and comprised about 17% of the total thickness of the cast film.
The coPEN was a copolymer of 70 mole % n~phth~lene dicarboxylate and 30 mole % dimethyl isophth~l~te. The viscosity of the coPEN was not measured.
The cast film was oriented in a manner con~i~tent with Example 1. The stretching was accomplished at 5.5 meters per minute (18 feet per minute) with an output width of 141 cm (55.5 inches). The stretch temperature was 154~C. The heat set tem~,.dlu~e was 164~C. The reslllt~nt film was 128 micrometers thick.
A Sharp C12P b~c~ ht was placed against the one face of a standard dichroic polarizer. The hllellsily of the light ra~i~ting from the b~ckli~ht/polarizer assembly was measured using a Photo research PR650 Spectra Colorimeter. The b~light/polarizer assembly is oriented relative to the detector of the PR650 prior to the start of the measurement such that the plane cont~ining the arc swept by the detector arm also contains the axis of high tr~n~mi.c~ion for the polarizer. Thedetector arm is swept plus and minus 60 degrees about a direction perpendicular to the backlight/polarizer assembly. A second intensity measurement was made with piece of film 23 cm square placed between the backlight and the polarizer such that the perpendicular tr~n~mi~ion axis of the film was coincident with the high trAncmic~ion direction of the polarizer. The ratio of the two intensities for each s angular position with the optical film in place to that without is reported as the Relative Gain.
The data for Example 136 is shown in Figure 9A. The average relative gain at the angles plus and minus 60 degrees from the normal was 1.45. This data demonstrates that the relative gain for the film of Example 136 increases at non-lo normal incident angles, particularly for angles from 30~ to 60~ away from normalincidence.

The following example illustrates the decrease in gain at non-normal 15 incident angles for a typical commercially available optical film A piece of microreplicated brightness enhancement film from Sekisui W5 18 (Osaka, Japan) was measured using the Eldim l 20D as described in Exa nple 136. The ratio of the intensities for each angular position with the Sekisui W5 18 film in place to that without the Sekisui film is shown as Figure 9B.
20 The average relative gain at the angles plus and minus 60 degrees from the normal was 0.65, indicating that the gain for the film peaks at normal incidence and declines for all angles away from normal incidence.
As demonstrated by Example 136 and Colllpa~ /e Example 1, films can be made in accordance with the present invention in which the relative gain 2s increases at non-normal incident angles, particularly for angles from 30~ to 60~
away from normal incidence. By contrast, the relative gain for commercially available optical films typically peaks at normal incidence and declines for allangles away from normal incidence. This feature of the films of the present invention make them particularly advantageous for use in applications such as 30 bri~htness t?nh~ncement films for large displays, where one will likely view the display across a wide range of angles.

. .
. .

The following examples further illustrate the increase in gain at non-normal angles of incidence achieved with the films of the present invention.
A series of examples were made in a manner similar to Example 136, s except that m~teri~l and process changes were made as indicated. In some of the exarnples, IrganoxTM 1425 antioxidant (available from Ciba Geigy) and/or DylarkTM
332-80 (available from NOVA Chemicals) were added. The average relative gain for the angles plus and minus 60 degrees from the normal as well as the relativegain at normal incidence (0 degrees) are reported in Table 6.

Ex. sPS % % Stretch Heat Relative Relative Irganox Dylark Temp. Set Gain Gain 1425 Temp. (0~) (+/- 60~) 137 30%, 0 0 160 164 1.18 1.40 138 30%, 0 0 154 199 1.21 1.48 139 30%, 0.5 2 154 199 1.20 1.46 140 30%, 0 2 154 199 1.18 1.47 141 15%, 0.5 0 154 199 1.15 1.48 142 15%, 0.5 0 154 199 1.21 1.47 143 30%, 0 0 154 199 1.16 1.47 144 30%, 0.5 0 154 199 1.29 1.47 145 30%, 0.5 0 154 199 1.06 1.35 146 30%, 0.5 2 154 199 1.13 1.43 147 30%, 0.5 2 154 164 1.21 1.47 148 30%, 0 2 154 164 1.17 1.47 149 15%, 0.5 0 154 164 1.21 1.47 150 30%, 0 0 154 164 1.23 1.38 W O 97/32225 PCT~US97/029g5 The prece-lin~ description of the present invention is merely illustrative, and is not inten~l~d to be limiting. Therefore, the scope of the present invention should be construed solely by reference to the appended claims.

., . , .. , _

Claims (66)

What is claimed is:
1. A light fixture, comprising:
a light source; and an optical element comprising a polymeric first phase and a second phase disposed within said first phase, said second phase being discontinuous along atleast two of any three mutually perpendicular axes;
wherein said first and second phases have indices of refraction which differ along a first axis by more than about 0.05 and which differ along a second axis orthogonal to said first axis by less than about 0.05,
2. The fixture of claim 1, wherein said optical element is a reflective element.
3. The fixture of claim 1, wherein said optical element is a polarizing element.
4. The fixture of claim 1, wherein said optical element is both a reflective element and a polarizing element.
5. The fixture of claim 1, wherein said fixture further comprises housing means for housing said light source and said optical element, and wherein said optical element is a reflective film disposed on an interior surface of said housing means.
6. The fixture of claim 1, wherein said fixture further comprises housing means for housing said light source and said optical element, wherein said housing means is equipped with at least one aperture for emitting light from said housing means, and wherein said optical element is disposed between said light source and said aperture.
7. The fixture of claim 6, wherein said optical element is a polarizer.
8. The fixture of claim 1, wherein said light source is a diffuse light source.
9. The fixture of claim 1, wherein said first phase has a birefringence of at least about 0.1.
10. The fixture of claim 1, wherein said first phase has a birefringence of at least about 0.15.
11. The fixture of claim 1, wherein said first phase has a birefringence of at least about 0.2.
12. The fixture of claim 1, wherein said second phase has a birefringence of less than about 0.02.
13. The fixture of claim 1, wherein said second phase has a birefringence of less than about 0.01.
14. The fixture of claim 1, wherein said second phase has an index of refractionwhich differs from said first phase by more than about 0.1 along said first axis.
15. The fixture of claim 1, wherein said second phase has an index of refractionwhich differs from said first phase by more than about 0.15 along said first axis.
16. The fixture of claim 1, wherein said second phase has an index of refractionwhich differs from said first phase by more than about 0.2 along said first axis.
17. The fixture of claim 1, wherein said second phase has an index of refractionwhich differs from said first phase by less than about 0.03 along said second axis.
18. The fixture of claim 1, wherein said second phase has an index of refractionwhich differs from said first phase by less than about 0.01 along said second axis.
19. The fixture of claim 1, wherein said optical elements have a total diffuse reflectivity along said at least one axis of at least about 50%

wherein said optical element has a total reflectivity of greater than about 50% for a first polarization of electromagnetic radiation and a total transmission of greater than about 50% for a second polarization of electromagnetic radiation orthogonal to said first polarization.
20. The fixture of claim 1, wherein said optical element has a total reflectivity of greater than about 60% for said first polarization of electromagnetic radiation.
21. The fixture of claim 1, wherein said optical element has a total reflectivity of greater than about 70% for said first polarization of electromagnetic radiation.
22. The fixture of claim 1, wherein said optical element has a total transmission of greater than about 60% for said second polarization of electromagnetic radiation.
23. The fixture of claim 1, wherein said optical body has a total transmission of greater than about 70% for said second polarization of electromagnetic radiation.
24. The fixture of claim 1, wherein at least about 40% of light polarized orthogonal to said first polarization of light is transmitted through said optical element with an angle of deflection of less than about 8°.
25. The fixture of claim 1, wherein at least about 60% of light polarized orthogonal to said first polarization of light is transmitted through said optical element with an angle of deflection of less than about 8°.
26. The fixture of claim 1, wherein at least about 70% of light polarized orthogonal to said first polarization of light is transmitted through said optical element with an angle of deflection of less than about 8°.
27. The fixture of claim 1, wherein said first phase comprises a thermoplastic resin.
28. The fixture of claim 27, wherein said thermoplastic resin is a syndiotactic vinyl aromatic polymer derived from a vinyl aromatic monomer.
29. The fixture of claim 27, wherein said thermoplastic resin comprises interpolymerized units of syndiotactic polystyrene.
30. The fixture of claim 27, wherein said thermoplastic resin comprises polyethylene naphthalate.
31. The fixture of claim 30, wherein said second phase comprises syndiotactic polystyrene.
32. The fixture of claim 27, wherein said second phase also comprises at least one thermoplastic polymer.
33. The fixture of claim 1, wherein said optical element is stretched to a stretch ratio of at least about 2.
34. The fixture of claim 1, wherein said optical element is stretched to a stretch ratio of at least about 4.
35. The fixture of claim 1, wherein said optical element is stretched to a stretch ratio of at least about 6.
36. The fixture of claim 1, wherein said first and second phases are immiscible.
37. The fixture of claim 1, wherein said second phase comprises a plurality of elongated masses whose major axes are substantially aligned along a common axis.
38. The fixture of claim 1, wherein said elongated masses have an aspect ratio of at least about 2.
39. The fixture of claim 1, wherein said elongated masses have an aspect ratio of at least about 5.
40. The fixture of claim 1, wherein said second phase comprises a plurality of rod-like structures.
41. The fixture of claim 1, wherein said optical element is stretched in at least two directions.
42. The fixture of claim 1, wherein said second phase is present in an amount of at least about 1% by volume relative to said first phase.
43. The fixture of claim 1, wherein said second phase is present in an amount of about 5% to about 50% by volume relative to said first phase.
44. The fixture of claim 1, wherein said second phase is present in an amount of about 15% to about 30% by volume relative to said first phase.
45. The fixture of claim 1, wherein said disperse phase is discontinuous along any three mutually perpendicular axes.
46. The fixture of claim 1, wherein the diffuse reflectivity of said optical elements along at least one axis for at least one polarization of visible, ultraviolet, or infrared electromagnetic radiation is at least about 30%.
47. The fixture of claim 1, wherein the extinction ratio of said optical element is greater than about 3.
48. The fixture of claim 1, wherein the extinction ratio of said optical element is greater than about 5.
49. The fixture of claim 1, wherein the extinction ratio of said optical element is greater than about 10.
50. The fixture of claim 1, wherein the optical element is a film, and wherein the index difference between said first and second phases is less than about 0.05 along an axis perpendicular to the surface of said film.
51. The fixture of claim 50, wherein the electromagnetic radiation is distributed anisotropically about the axis of specular reflection.
52. The fixture of claim 51, wherein said optical element is stretched in at least one direction, and wherein the diffusely reflected portion of said at least one polarization of electromagnetic radiation is distributed primarily along or near the surface of a cone whose axis is centered on the stretch direction and whose surface contains the specularly reflected direction.
53. The fixture of claim 51, wherein said second phase comprises elongated inclusions whose axes of elongation are aligned in a common direction, wherein said optical element is stretched in at least one direction, and wherein the diffusely reflected portion of said at least one polarization of electromagnetic radiation is distributed primarily along or near the surface of a cone whose axis is centered on the axis of elongation direction and whose surface contains the specularly reflected direction.
54. The fixture of claim 50, wherein the electromagnetic radiation is distributed anisotropically about the axis of specular transmission.
55. The fixture of claim 1, wherein said optical element is stretched in at least one direction, wherein at least about 40% of light polarized orthogonal to said polarization of light is diffusely transmitted through said optical element, and wherein said diffusely transmitted rays are distributed primarily along or near the surface of a cone whose surface contains the spectrally transmitted direction and whose axis is centered on the stretch direction.
56. The fixture of claim 1, wherein said second phase comprises elongated inclusions whose axes of elongation are aligned in a common direction, wherein said optical element is stretched in at least one direction, and wherein the diffusely transmitted portion of said at least one polarization of electromagnetic radiation is distributed primarily along or near the surface of a cone whose axis is centered on the axis of elongation direction and whose surface contains the diffusely transmitted direction.
57. The fixture of claim 1, wherein the optical element is a film, and wherein the index difference between said first and second phases is less than about 0.02 along an axis perpendicular to the surface of said film.
60. In combination with a light source, an optical element (~0) body comprising:
a first phase (~2) having a birefringence of at least about 0.05; and a second phase, (~~) disposed within said first phase;

wherein the absolute value of the difference in index of refraction of said first and second phases is .DELTA.n1 along a first axis and .DELTA.n2 along a second axis orthogonal to said first axis, wherein the absolute value of the difference between .DELTA.n1 and .DELTA.n2 is at least about 0.05, and wherein the diffuse reflectivity of said first and second phases taken together along at least one axis for at least one polarization of electromagnetic radiation is at least about 30%.
59. The optical element of claim 58, wherein wherein the absolute value of the difference between .DELTA.n1 and .DELTA.n2 is at least about 0.1.
60. The optical element of claim 58, wherein said first phase has a larger birefringence than said second phase.
61. The optical element of claim 60, wherein the birefringence of said first phase is at least 0.02 greater than the birefringence of said second phase.
62. The optical element of claim 60, wherein the birefringence of said first phase is at least 0.05 greater than the birefringence of said second phase.
63. The optical element claim 58 having a plurality of layers, wherein at least one of said plurality of layers comprises:
a first phase having a birefringence of at least about 0.05; and a second phase which is discontinuous along at least two of any three mutually orthogonal, wherein the absolute value of the difference in index of refraction of said first and second phases is .DELTA.n1 along a first axis and .DELTA.n2 along a second axis orthogonal to said first axis, wherein the absolute value of the difference between .DELTA.n1 and .DELTA.n2 is at least about 0.05, and wherein the diffuse reflectivity of said first and second phases taken together along at least one axis for at least one polarization of electromagnetic radiation is at least about 30%.
64. The light fixture, of claim 58 comprising:
a light source; and an optical film;
wherein said optical film comprises a polymeric first phase and a second phase disposed within said first phase, said second phase being discontinuous along atleast two of any three mutually perpendicular axes;
wherein said first and second phases have indices of refraction which differ along a first axis by more than about 0.05 and which differ along a second axis orthogonal to said first axis by less than about 0.05.
65. A light fixture, comprising:
a light source;
reflecting means for reflecting light produced by said light source; and polarizing means for polarizing light produced by said light source;
wherein at least one of said reflecting means and said polarizing means comprises a polymeric first phase (~2) and a second phase (~6) disposed within said first phase, said second phase being discontinuous along at least two of any three mutually perpendicular axes, and wherein said first and second phases have indices of refraction which differ along a first axis by more than about 0.05 and which differ along a second axis orthogonal to said first axis by less than about 0.05, wherein the diffuse reflectivity of said first and second phases taken together along at least one axis for at least one polarization of electromagnetic radiation is at least about 30%.
66. method for obtaining a diffuse reflective polarizer, comprising the steps of: providing a first resin, whose degree of birefringence can be altered by application of a force field.
as through dimensional orientation or an applied electric field, such that the resulting resin material has, for at least two orthogonal directions, an index of refraction difference of more than about 0.05; providing a second resin, dispersed within the first resin; and applying said force field to the composite of both resins such that the indices of the two resins are approximately matched to within lessthan about 0.05 in one of two directions, and the index difference between first and second resins in the other of two directions is greater than about 0.05. ) -95a-
CA002248237A 1996-02-29 1997-02-28 Light fixture containing optical film Abandoned CA2248237A1 (en)

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US08/610,092 US5825543A (en) 1996-02-29 1996-02-29 Diffusely reflecting polarizing element including a first birefringent phase and a second phase

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CA002246545A Abandoned CA2246545A1 (en) 1996-02-29 1997-02-28 Optical fiber with light extractor
CA002246449A Abandoned CA2246449A1 (en) 1996-02-29 1997-02-28 Optical film with increased gain at non-normal angles of incidence
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CA002246449A Abandoned CA2246449A1 (en) 1996-02-29 1997-02-28 Optical film with increased gain at non-normal angles of incidence

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