CA1324749C - Flexible stretch/shrink film - Google Patents
Flexible stretch/shrink filmInfo
- Publication number
- CA1324749C CA1324749C CA000553184A CA553184A CA1324749C CA 1324749 C CA1324749 C CA 1324749C CA 000553184 A CA000553184 A CA 000553184A CA 553184 A CA553184 A CA 553184A CA 1324749 C CA1324749 C CA 1324749C
- Authority
- CA
- Canada
- Prior art keywords
- film
- layer
- low density
- layers
- density polyethylene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/05—5 or more layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
- B32B2323/046—LDPE, i.e. low density polyethylene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2553/00—Packaging equipment or accessories not otherwise provided for
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/91—Product with molecular orientation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31913—Monoolefin polymer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31928—Ester, halide or nitrile of addition polymer
Abstract
ABSTRACT OF THE DISCLOSURE
A multi-layered thermoplastic polyolefin film having an im-proved combination of physical characteristics is disclosed. In particu-lar, the multi-layered film evidences an improved combination of abuse resistance, elongation, and flexibility. Preferred five layer em-bodiments of the film comprise (1) a core layer of very low density poly-ethylene; (2) two adjacent intermediate layers of a linear low density polyethylene and (3) two outer layers of an ethylene vinyl acetate copolymer or very low density polyethylene.
A multi-layered thermoplastic polyolefin film having an im-proved combination of physical characteristics is disclosed. In particu-lar, the multi-layered film evidences an improved combination of abuse resistance, elongation, and flexibility. Preferred five layer em-bodiments of the film comprise (1) a core layer of very low density poly-ethylene; (2) two adjacent intermediate layers of a linear low density polyethylene and (3) two outer layers of an ethylene vinyl acetate copolymer or very low density polyethylene.
Description
32474q FLEXIBLE STRETCH/SHRINK FILM
FIELD OF TH~ INVENTION -The pre~ent invention relates to a heat shrinkable, thermoplastic packaging film. In particular, the invention provldes ln a multllayer thermoplastlc packaglng film havlng at least flve layer~, lncluding a layer o$ llnear low denslty polyethylene, the improvement whereinl (a) a core layer comprl~es a very low denslty polyethylene;
(b) lntermedlate layers adjacent each slde o$ the core layer comprise a linear low denslty polyethylene; and (c) two outer layers each bonded to a respective intermediate layer comprise a very low denslty polyethylene;
whereln the film has a modulus at 73F of less than about 17,000 pBi in the longitudinal and transverse directlon.
BACKGROUND O~ THE INVENTION
The preæent inventlon i8 dlrected to new and useful multllayer heat shrinkable film formulations. One dlstlngulshing ~- ~
feature of a shrink fllm i8 the film's ability, upon exposure to a ~ ;--certain temperature, to shrink, or, if restralned from shrlnking, to generate shrlnk tension within the film.
The manufacture of shrlnk fllms, as is well known in the art, may be generally a¢complished by extrusion (single layer ~-films) or coextrusion (multilayer films) of thermopla3tic resinous ;
material~ which have been heated to their flow or melting po~nt from an ex~rusion or coextrusion die in, for example, elther tubular or planar ~sheet) form. -~
`` 1 324749 After a post extrusion quenching to cool by, for example, the well-known cascading water method, the relatively thick "tape" extrudate is then reheated to a temperature within its orientation temperature range and stretched to orient or align the crystallites and/or molecules of the material. The orientation temperature range for a given material or materials will vary with the different resinous polymers and/or blends thereof which comprise the material. However, the orientation tempera-ture rang~ for a given thermoplastic material may generally be stated to be below the crystalline melting point of the material but above the second order transition temperature (sometimes referred to as the glass transition point) thereof. Within this temperature range it is easy to effectively orient the material.
The terms "orientation" or "oriented" are used herein to generally describe the process step and resultant product characteristics obtained by stretching and immediately cooling a resinous thermoplastic polymeric material which has been heated to a temperature within its orientation temperature range so as to revise the inter-molecular config-uration of the material by physical alignment of the crystallites and/or molecules of the material to improve certain mechanical properties of the film such as, for example, shr~nk tension and orientation release stress.
Both of these properties may be measured in accordance with ASTM D 2838-81. When the stretching force is applied in one direction uniaxial orientation results. When the stretching force is applied in two -directions biaxial orientation results. The term oriented is also herein used interchangeably with ~he term "heat shrinkable" with these terms de-signating a material which has been stretched and set by cooling while sub-stantially retaining its stretched dimensions. An oriented (i.e. heat I shrinkable) material will tend to return to its original unstretched (un-¦ extended) dimensions when heated to an appropriate elevated temperature.
Returning to the basic process for manufacturing the film as I discussed above, it can be seen that the film, once extruded (or ¦ coextruded if it is a multi-layer film) and initially cooled by, for example, cascading water quenching, is then reheated to within its orientation temperature range and oriented by stretching. The stretching ~2 .
to orient may be accomplished in many ways such as, for example, by "blown bubble" techniques or "tenter framing". These processes are well known to those in the art and refer to orientation procedures whereby the material is stretched in the cross or transverse direction (TD) and/or in the longitudinal or machine direction (MD). After being stretched, the film is quickly quenched while substantially retaining its stretched dimensions to rapidly cool the film and thus set or lock-in the oriented molecular configuration.
Of course, if a film having little or no orientation is de-sired, e.g. non-oriented or non-heat shrinkable film, the film may be formed from a non-orientable material or, if formed from an orientable material may be "hot blown". In forming a hot blown film the film i9 not cooled immediately after extrusion or coextrusion but rather is first stretched shortly after extrusion while the film is still at an elevated temperature above the orientation temperature range of the material.
Thereafter, the film is cooled, by well-known methods. Those of skill in the art are well familiar with this process and the fact that the result-ing film has substantially unoriented characteristics. Other methods for forming unoriented films are well known. Exemplary, is the method of cast extrusion or cast coextrusion which, likewise, is well known to those in the art.
After setting the stretch-oriented molecular configuration the film may then be stored in rolls and utilized to tightly package a wide variety of itemæ. In this regard, the product to be packaged may first be enclosed in the heat shrinkable material by heat sealing the shrink film to itself where neceæsary and appropriate to form a pouch or bag and then inserting the product therein. If the material was manufactured by "blown bubble" techniques the material may still be in tubular form or it may have been slit and opened up to form a sheet of film material.
Alternatively, a sheet of the material may be utilized to over-wrap the product. These packaging methods are all well known to those of skill in the art. Thereafter, the enclosed product may be subjected to elevated temperatures by, for example, passing the enclosed product through a hot air or hot water tunnel. This causes the enclosing film to shrink around the product to produce a tight wrapping that closely conforms to the ', ' "`,`"' - 1 3 2 4 ~ ~ 9 64536-630 contour of the product. As stated above, the fllm sheet or tube may be formed lnto bags or pouches and thereafter utllized to psckage a produc~.
In thls case, lf the film has been formed as 8 tube lt may be prefersble to first sllt the tubular fllm to form a fllm sheet and thereafter form the ~heet lneo bags or pouches. Such beg or pouch formlng methods, llkewlse, are well known to those of sklll in the art.
The above general outllne for manufacturlng of fllms 19 not meant to be all lncluslve slnce such processes are well known to those ln the art. For example, see U.S. Patent Nos. 4,274,900; 4,229,241;
4,194,039; 4,188,443; 4,048,428; 3,821,182 flnd 3,022,543. The dlsclo-sure6 of these patents are generally representatlve of such processes .
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: : -Alternatlve methods oE produclng films of thls type are knownto those ln the art. One well-known alternative ls the methad of formlng 15 a multi-layer fllm by an extruslon coatlng rather than by an extruslon or ~ -coextruslon process as was di~cussed above. In extruslon coatlng a flrst tubular layer 1B extruded and thereafter sn addltlonal layer or layers ls sequentlally coated onto the outer surface of the flrst tubular layer or a successlve layer. Exemplary of thls method is U.S. Pat. No. 3,74l,253.
Thls patent 19 generally representatlve of an extruslon coating process.
, ' ' '' , ,, : ', ' Msny other process varlatlons for formlng fllms are well known l~ to those in the art. For example, multlple layers may be flrst ¦~ coextruded wlth addltlonsl layers thereafter belng extrusion coated - 25 thereon. Or two multl-layer tubes may be coextruded wlth one of the tubes thereafter belng extruslon coated or laminated onto the other. The extrusion coatlng method of film formation is prefer~ble to coextrudlng the entlre film when lt ls deslred to sub~ect one or more layers of the film to fl treatment which may be harmful to one or more of the other layers. Exe~plary of such a situation is a case where it 18 deslred to l~ irradlate one or more layers of a film contalnlng an oxygen barrler layer j comprised of one or more copolymers of vlnylldene chlorlde and vlnyl chlorlde. Those of sklll in the art generally recognlze that lrradlatlon l ls generaliy harmful to such oxygen barrler layer composltions. Accord-, ~
, ~ .
1 32474~
lngly, by means of extruslon coatlng, one may flrfit extrude or coextrude a flrst layer or layers, subJect that layer or layers to lrradlAtlon and thereafter extruslon cost the oxygen ~arrler layer and, for that matter, other layers sequentially onto the outer surface of the extruded prevl-ously lrradlated tube. Thls sequence allows for the lrradlatloncross-llnking of the flrst layer or layers wlthout sub~ectlng the oxygen barrier layer to the harmful effect~ thereof.
Irradlation of an entlre film or a layer or layers thereof may be deslred 80 as to lmprove the film's reslstance to abuse and/or puncture and other phy~lcal characterlstics. It 18 generally well known ln the art that lrradlatlon of certaln fllm materlals results ln the cross-llnklng of the polymerlc molecular chalns contained thereln and that such action generally results in a material having improved abuse re61stance.
Irradiatlon may be accompllshed by the use of hlgh energy electrons, ultra vlolet radiation, X-rays, gammA rsys, beta particles, etc. Prefersbly, electrons are employed up to about 20 megarads (MR) dosage level. The lrradlation source can be any electron beam generfltor operatlng in a range of about 150 kllovolts to about 6 megavolts wlth a power output capable of supplylng the desired dosage. The voltage can be ad~usted to approprlflte level~ whlch may be for example l,000,000 or 2,000,000 or 3,000,000 or 6,000,000 or higher or lower. Many apparatus for irradiatlng fllms are known to those of ~kill ln the art. The lrrndlatlon ls usually carrled out at a dosage between about 1 MR and about 20 MR, with a preferred dosage range of about 2 MR to about 12 MR. Irradlatlon can be carried out conveniently at room temperature, although higher and lower temperaturec, for exsmple, 0 ~o 60 may be employed.
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Cross-linking may also be accompllshed chemlcally through utlllzation of peroxldes a~ is well known to those of sklll ln the art.
A general dlscu6slon of cross-llnklng can be found at pages 331 to 414 of volume 4 of the Encyclopedla of Polymer Sclence and Technology, Pl~stlc6, Reslns, Rubber~, Plber8 publlshed by John Wlley b Sons, Inc. and copy-rlghted ln 1966. Thi~ document has a Library of Congre~s Cfltalog Card Number of 64-22188- -,.. ,' ~
Another possible processing variation is the application of a fine mist of a silicone or anti-fog spray to the interior of the freshly extruded tubular material to improve the further processability of the tubular material. A method and apparatus for accomplishing such internal application is disclosed in U.S. Patent No. 4,612,245.
The polyolefin family of shrink films and, in particular, the polyethylene family of shrink films provide a wide range of physical and performance characteristics such as, for example, shrink force (the amount of force that a film exerts per unit area of its cross-section during shrinkage), the degree of free shrink (the reduction in linear dimension in a specified direction that a material undergoes when sub-jected to elevated temperatures while unrestrained), tensile strength (the highest force that can be applied to a unit area of film before it begins to tear apart), heat sealability, shrink temperature curve (the relation-ship of shrink to temperature), tear initiation and tear resistance (theforce at which a film will begin to tear and continue to tear), optics (gloss, haze and transparency of material), elongation (the degree the film will stretch or elongate at room temperature), elastic memory (the degree a film will return to its original unstretched (unelongated) dimension after having been elongated at room temperature), and dimen-sional stability (the ability of the film to retain its original dimensionæ under different types of storage conditions). Film charac-teristics play an lmportant role in the selection of a particular film and they differ for each type of packaging application and for each type of package. Consideration must be given to the product size, weight, shape, rigidity, number of product components and other packaging materi-i als which may be utilized along with the film material and the type of packaging equipment available.
' ~ In view of the many above-discussed physical characteristics i :~ 30 which are associated with polyolefin films and films containing a polyolefin constituent and in further view of the numerous applications with which these films have already been associated and those to which they may be applied in the future, it is readily discernable that the need for ever improving any or all of the above described physical characteristics or combinations thereof in these films is great, and, .' naturally, ongoing. In particular, the quest for a heat shrinkable polyethylene film having an improved combination of elongation, abuse resistance, and flexibility has been ongoing since such a film could compete well in the trayed product (for example, meat such as poultry parts) over-wrap market. Historically, polyvinyl chloride (PVC) films have beenutilized in this overwrap application because of their good degree of elongation and elastic memory. PVC was superior to conventional heat shrinkable films with regard to overwrapped trayed products which were subject to moisture loss because the PVC was elastic and continued to contract as the product lost moisture and shrank during the distribution cycle. The result was a tight package which was somewhat unattractive because it was leaky. The elasticity of PVC also allowed automatic over-wrapping machinery to stretch the PVC material about the trayed product during overwrapping of the product and the associated tray. In spite of the fact that the package was leaky, PVC proved superior to conventional heat shrink packages because such conventional packaging materials possessed relatively poor elasticity or elastic memory. Thus, when a product wrapped in such a material shrank from moisture loss during the distribution cycle the film did not also shrink and the result was a loose package having a shopworn appearance.
Unfortunately, PVC has several drawbacks associated therewith which those in the art wish to improve upon or wholly eliminate. Exem-I plary of these drawbacks is the fact that PVC tray overwrap film general-¦ ly evidences both (1) poor seal integrity and (2) poor abuse resistance.
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25The poor seal integrity of PVC overwrap films arises at least I in part from the fact that the PVC material in PVC overwrapped trays is j tack welded to itself as opposed to being hermetically sealed. Thus, the liquid purge or juices which exude from the overwrapped trayed meat products will leak through a tack sealed PVC overwrapped tray and result 130 in a package that is unsightly and messy from a consumer viewpoint. This ¦drawback appears to be irreconcilably linked to PVC since attempts to Ihermetically seal PVC in a commercial tray overwrap environment usually result in "burn-through" of the PVC material.
Il 7 , ,, . ; . , ~ ., . . , . - - . .. .. ~ . . , , . ., .. " . , , , . . . . . - ., .
. , ... . ., , . , . . .. ,. . - ; . ,, - ~. , ., .. ~ , Another maJor drawback of PVC tray overwrap materlal 19, AS
stated above, the material's poor reslstance to abuse. In this regard the PVC materlnl tends to tear along the edges of the overwrapped tray lf rubbed durlng tr~n~lt by another tray or ~n encloslng carton.
Past attempts to produce a heat shrlnkable polyolefln fllm whlch po~sesses 6atlsfactory elongatlon and elastic memory have resulted ln a fllm which 19 deflclent ln lts resis~ance to tear propagation. That is to say the fllm has the téndency to tear rapidly or "zlpper" once punctured. The "21pperlng" problem ls of great concern slnce thls tralt substantlally reduces the utllity of a fllm for nppllcations lnvolvlng automatlc packaglng equlpment. Zlppered fllm results ln increased down tlme. Heat shrlnkable polyolefln films havlng lmproved abuse resls- -tance are known to those ln the art. Recent developments include the fllm descrlbed ln U. S. Patent No. 4,617,241 whlch has provlded a satls-factory comblnatlon of deslred physlcal characterlstics ln that the fllm evldences a new and lmproved comblnatlon of phy~lcal characterlstlcs--e.g.
heat shrlnkablllty, elongatlon, elastic memory, heat sealablllty and abuse reslstance (puncture reslstance and reslstance to tear propagation).
However, as useful as these recent fllms have proven ln stretch/
shrink packaging appllcatlons, ln certaln appllcatlons lt 18 deslrable to provlde a multllayer fllm whlch ln some cases provides even better elonga-tlon characterlstics, lmproved abuse characterlstics, and a lower modulus (i.e. higher flexlblllty) film which wlll improve machlnablllty.
AIMS OF THE PRESENT INVENTION
, Accordlngly, the present invention seeks to provlde a trny overwrap polyolefin fllm that wlll be an lmprovement over the prior art tray overwrap fllms.
The present invention also seeks to provide a :.
polyolefln tray overwrap fllm havlng a deslred new and lmproved comblna-30 tion of phy8ical characterl8tlc8 such as, for example, abuse re~lstance, elongatlon and flexlblllty.
'~' .
64s36-63n The present invention also seeks to provide a five layer polyolefln fllm havlng an lnterlor core layer comprislng a very low denslty polyethylene; two ~dJacent lntermediate lnyers compri61ng a llne~r low den~lty polyetllylene and two outer layers comprising el~her an ethylene vinyl acetate copolymer or n very low density polyethylene.
The broad scope of applicability of the pre6ent invention wlll become apparent to tho6e of ordlnary 6klll ln the art from the detall6 dlsclo6ed herelnafter. However, lt should be understood that the followlng detalled descrlptlon whlch lndlcate6 several preferred embodlments of the present lnventlon ls only glven for purpo6es of lllustratlon slnce varlous changes and modlflcatlons well wlthln the ~cope of the present lnventlon wlll become apparent to tho6e of ordlnary ~klll ln the art ln vlew of the following detalled descrlption.
,,.--~.....
DEFINITIONS ;:~
"
Unless speclficslly set forth and defined or otherwise limited, the terms "polymer" or "polymer resin" a8 used herein generally lnclude`, but are not llmited to, homopolymers, copolymers, such as, for example block, graft, random and alternatlng copolymers, terpolymers etc. and blends and modlficstlons thereof. Furthermore, unles6 otherwlse speclfi-cslly llmlted the terms "polymer" or "polymer resln" shall lnclude all possible symmetrlcal structures of the materlsl. These structure6 lnclude, but are not llmlted to, lsotactic, syndlotactic flnd random ~ymmetrles.
.
The terms "melt flow" as uaed hereln or "melt flow lndex" ls the amount, ln grams, of a thermoplastlc re61n whlch can be forced through a given oriflce under a speclfied pre6sure and temperature wlthin ten minutes. The value 6hould be determined ln accordance wlth ASTM D
1230.
.' '. ' 404/ô70310/4/9 q '.. .
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- 1 32474q The terms "outer" or "outer layer" as used herein mean a layer of a multi-layer film which normally comprises a surface thereof in a five-layer embodiment or at least lies outside of the intermediate and core layers.
The term "core" or "core layer" as used herein usually refers to an interior layer of a multi-layer film having an odd number of layers wherein the same number of layers is present on either side of the core layer. In films having an even number of layers, the core layer can be either of the two central layers.
The term "intermediate" or "intermediate layer" as used herein refers to an interior layer of a multi-layer film which is positioned between a core layer and an outer layer of said film.
The term polyolefin as used herein refers to polymers of relatively simple olefins such as, for example, ethylene, propylene, butenes, isoprenes and pentenes; including, but not limited to, homopolymers, copolymers, blends and modifications of such relatively simple olefins.
The term "polyethylene" as used herein refers to a famlly of resins obtalned by polymerizing the gas ethylene, C2H4. By varying the catalysts and methods of polymerization, properties such as density, melt index, crystallinity, degree of branching and cross-linking, molecular weight and molecular weight distribution can be regulated over wide 1 ranges. Further modifications are obtained by copolymerization, chlori-¦ nation, and compounding additives. Low molecular weight polymers of i~ 25 ethylene are fluids used as lubricants; medium weight polymers are waxes ¦ miscible with paraffin; and the high molecular weight polymers (generally i over 6,000) are resins generally used in the plastics industry. Polyeth-~ ylenes having densities ranging from about 0.900 g/cc to about 0.940 g/cc i are called low density polyethylenes while those having densities from 1 30 about 0.941 g/cc to about 0.965 g/cc and over are called high density¦ polyethylenes. The low density types of polyethylenes are usually polymerized at high pressures and temperatures whereas the high density types are usually polymerized at relatively low temperatures and pressures.
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1 3247~9 The term "linear low density polyethylene" (LLDPE) as used herein refers to copolymers of ethylene with one or more comonomers selected from C4 to C10 alpha olefins such as butene-l, octene, etc. in which the molecules thereof comprise long chains with few side chains branches or cross-linked structures. The side branching which is present will be short as compared to non-linear polyethylenes. Linear low density polyethylene has a density usua]ly in the range of from about 0.916 g/cc to 0.940 g/cc for film making purposes. The melt flow index of linear low density polyethylene generally ranges from between about 0.1 to about 10 grams per ten minutes and preferably between from about 0.5 to about 3.0 grams per ten minutes. Linear low density polyethylene resins of this type are commercially available and are manufactured in low pressure vapor phase and liquid phase processes using transition metal catalysts.
The term "very low density polyethylene" (VLDPE) is used herein to describe a linear ethylene-alpha-olefin copolymer having densities of generally between 0.890 and O.91S grams/cubic centimeter, and produced by cataly~ic, low pressure processes.
The term "ethylene vinyl acetate copolymer" (EVA) as used herein refers to a copolymer formed from ethylene and vinyl acetate monomers wherein the ethylene derived units in the copolymer are present in ma;or amounts and the vinyl acetate derived units in the copolymer are present in minor amounts.
An "oriented" or "heat shrinkable" material is defined herein as a material which, when heated to an appropriate temperature above room temperature ~for example 96C), will have a free shrink of 5% or greater in at least one linear direction.
All compositional percentages used herein are calculated on a "by weight" basis. `
Free shrink should be measured in accordance with ASTM D 2732.
..
The elongation properties of the film should be measured in accordance with ASTM D 638.
~` :
5~
A "cross-llnked" materlal as used herein shall be deflned as a materlal whlch after refluxlng ln bolllng toluene or xylene, as approprlate, for forty (40~ hours shall have a welght percent residue of at least 5 percent. A procedure for determlnlng whether a materlal ls cross-llnked vel non is to reflux 0.4 gram of the materlal ln bolllng toluene or another approprlate solvent, for example xylene, for twenty (20) hours.
If no lnsoluble resldue (gel) remalns the materlal ls determlned not to be cross-llnked. If, after twenty (20) hours of refluxlng lnsoluble resldue (gel) remalns the materlal is refluxed under the same condltlons for another twenty (20) hours. If more than 5 welght percent of the materlal remalns upon concluslon of the ~econd refluxlng the materlal ls consldered to be cross-linked.
¦ Preferably, at least two repllcates are utlllzed.
j A rad ls the quantlty of lonlzlng radlatlon that results ¦ ln the absorptlon of 100 ergs of energy per gram of a radlated -materlal, regardless of the source of the radiatlon. A megarad 19 ~ 106 rads. (MR ls an abbrevlatlon for megarad).
¦ SUMMARY OF THE INVENTION
It has been dlscoverd that a flexlble, heat shrlnkable thermoplastlc packaglng fllm havlng a deslrable comblnatlon of physlcal characterlstlcs such as, elongatlon, abuse reslstance, flexlblllty, and heat shrlnkablllty has been achleved by the multllayer flexlble, thermoplastlc packaglng film of the present lnventlon. This multllayer fllm comprlses a core layer comprislng ;~
,' " - .
`'.':
1 32474~
very low density polyethylene, intermediate layers adjacent each -~
~lde of the core layer compri~iing a linear low denslty polyethylene, and two outer layers each bonded to a respectlve intermediate layer, and compri~iing very low denslty polyethylene.
Preferably, the multilayer fllm is both orlented and lrradlated.
Preferably the $ilm has a modulus of less than about 17,000 p8i ln the longltudinal direction and les~ than about 13,000 psi in the transverse dlrectlon. A1BO preferably the elongation of the film at break at 73F loi at least about 220% ln the longltudlnal dlrectlon and at lea~t about 250% in the tran~verse dlrectlon.
12a 1 32474q BRIEF DESCRIPTION OF THE DRAWING
Figure I is a cross-sectional view of a preferred five layered embodiment of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring to Figure I, which is a cross-sectional view of a five layered preferred embodiment of the present invention, it is seen that this embodiment comprises a core layer 1, two ad~acent intermediate layers 2 and 3 and two skin or surface layers 4 and 5. The preferred thickness ratio of the five layers of 1/1.5/1/1.5/1 is demonstrated in Figure I. A preferred core layer 1 formulation comprises very low density polyethylene.
' ' .
Our experimentation has revealed an especially preferred core layer formulation is very low density polyethylene which may be obtained from Dow Chemical Company under the trade designation XU61512.08L. This resin is believed to have a density at 23C of about 0.905 gm/cm3 and a melt flow rate (measured by condition E) of about .8 gm/10 min. Other very low den~ity polyethylenes may be utilized to form the core layer 1, for example DSM 2H286 available from Dutch State Mines.
'~
Returning to Figure I, and in particular, ad~acent intermediate layers 2 and 3 it has been determined that a preferred intermediate layer formulation should comprise a linear low density polyethylene material.
A preferred linear low density polyethylene is Dowlex 2045.04. Other linear low tensity polyethylene materials or blends of two or more linear low density polyethylene materials may be utilized to form the intermediate layers 2 and 3. Preferably the composition of intermediate lay0rs 2 and 3 is the same, however, different linear low density polyethylenes or - blends thereof may be utilized for each intermediate layer. Dowlex 2045.04 is believed to have a density of about 0.920 gm/cm3 and a flow rate ~measured by condition E) of from about 0.7 to 1.2 gm/ten minutes.
..
~, . .
With rega~d to outer layers 4 and 5 it has been determined that a preferred skin layer formulation comprises either a copolymer of ethylene and vinyl acetate, or very low density polyethylene. VLDPE utilized to form the core layer 1 may, preferably, be the same material as that which is utilized to form the two outer layers 4 and 5. A particularly preferred outer layer ethylene vinyl acetate copolymer is PE204CS284. This resin is available ~rom El Paso Polyolefins Company, and is believed to have a density at 23C of from about 0.9232 grams/cubic centimeter to about 0.9250 grams/cubic centimeter and a melt flow rate (measured by condition E) of about 2.0 grams/10 minutes. Other ethylene vinyl acetate copolymers or blends of two or more ethylene vinyl acetate copolymers may be utilized to form outer layers 4 and 5. Preferably the composition of outer layers 4 and 5 is the same, however, different VLDPE resins or blends thereof, and different ethylene vinyl acetate copolymers or blends thereof, may be utilized for each outer layer.
Those skilled in the art will ~eadily recognize that all of the above disclosed, by weight, percentages are subject to slight variation.
Additionally, these percentages may vary slightly as a result of the inclusion or application of additives such as the silicone mist discussed above or agents such as slip and anti-block agents. A preferred anti-block agent is silica which is available from Johns Manville under the trade-name White Mist. Preferred slip agents are erucamide (available ' from Humko Chemical under the trade-name Kemamide E), and stearamide ¦ (available from the Humko Chemical Company under the trade-name Kemamide S) and N, N-' dioleoylethylenediamine (available from Glyco Chemical under the trade-name Acrawax C). A preferred silicone spray is a liquid polyorganosiloxane manufactured by General Electric under the trade designation General Electric SF18 polydimethylsiloxane.
The general ranges for inclusion or, in the case of the 1 30 silicone spray, the application of these additives are as follows:
; (1) silica: 250-3000 ppm (2) N, N-' dioleoylethylenediamine: 200-4000 ppm (3) erucamide: 200-5000 ppm (4) stearamide: 200-5000 ppm (5) silicone spray: 0.5 mg.ft2-and up 1~ .
When utilized within the specification and claims of the present application the term "consisting essentially of" is not meant to exclude slight percentage variations or additives and agents of this sort.
Additional layers and/or minor amounts of additives of the types described above may be added to the film structure of the present invention as desired but care must be taken not to adversely affect the desirable physical properties and other characteristics of the inven-tive film.
In the preferred process for making the multi-layer film of the present invention the basic steps are coextruding the layers to form a multilayer f ilm, irradiating the f ilm, and then stretching the f ilm to biaxially orient. These steps and additional desirable steps will be explained in detail in the paragraphs which follow.
The process begins by blending, if necessary, the raw materials (i.e. polymeric resins) in the proportions and ranges desired as dis-cussed above. The resins are usually purchased from a supplier in pellet form and can be blended in any one of a number of commercially available blenders as is well known in the art. During the blending process any additives and/or agents which are desired to be utilized are also incorporated.
The resins and applicable additives and/or agents are then fed to the hoppers of extruders which~--feed a coextrusion die. For the preferred five-layer film having two identical outer layers and two identical intermediate layers at least 3 extruders need to be employed, one for the two outer layers, one for the two intermediate layers and one for the core layer. Additional extruders may be employed if a film having non-identical outer layers or non-identical intermediate layers is desired.
The materials are coextruded as a relatively thick tube or "tape" which has an initial diameter dependent upon the diameter of the coextrusion die. The final diameter of the tubular film is dependent upon the racking ratio, e.g.
the stretching ratio. Circular coextrusion dies are well known to tho~e in the art and can be purchased from a number of manufacturers. In addition to 404/870310/4/15 -~
,: ~
-:: 1 3247~q tubular coextrusion, slot dies could be used to coextrude the material in sheet form. Well known single or multi-layer extrusion coating processes could also be utilized, if desired.
:
An additional process step which should be utilized to manufac-ture the preferred embodiment of the presently inventive film is to irradiate the tape or unexpanded tubing or sheet by bombarding it with high-energy electrons from an accelerator to cross-link the materials of ¦ the tube. Cross-linking greatly increases the structural strength of the I film or the force at which the material can be stretched before tearing! lo apart when the film materials are predominately ethylene such as polyeth-ylene or ethylene vinyl acetate. Irradiation also improves the optical properties of the film and changes the properties of the film at higher temperatures. A preferred irradiation dosage level is in the range of from about 0.5 MR to about 12.0 MR. An even more preferred range is from about 4 MR to about 8 MR. The most preferred dosage level is approximately 7 to 8 MR.
~i Following coextrusion, quenching to cool and solidify, and irradiation of the tape, the extruded tape is reheated and inflated into a bubble by application of internal air pressure thereby transforming the narrow tape with thick walls into a wide film with thin walls of the desir-ed film thickness and width. This process is sometimes referred to as the "trapped bubble technique" of orientation or as "racking". The degree of inflation and subsequent stretching is often referred to as the "racking ratio" or "stretching ratio". For example, a transverse racking or stretch-ing ratio of 2.0 would mean that the film had been stretched 2.0 times itsoriginal extruded size in the transverse direction during transverse rack-ing. After stretching, the tubular film is then collapsed into a super-imposed lay-flat configuration and wound into rolls often referred to as "mill rolls". The racking process orients the film by stretching it trans-versely and longitudinally and thus imparts shrink capabilities to the film.Additional longitudinal or machine direction racking or stretching may be accomplished by revolving the deflate rollers which aid in the collapsing of the "blown bubble" at a greater speed than that of the rollers which serve to transport the reheated "tape" to the racking or blown bubble area.
~ ':
3~ 404/870310/4/16 li r,~" .~ ; . - . . ',. '.'. " . ' : . . ' ' .
Preferred transverse and longitudinal stretching ratios of the present film range from between about 2.5 trans-verse by about 3.0 longitudinal to about 5.0 transverse and about 5.0 longitudinal. A particularly preferred stretching ratio is about 3.0 to 4.0 transverse by about 3.0 to 4.0 longitudinal. All of these methods of orientation are well known to those of skill in the art.
To further disclose and clarify the scope of the present invention to those skilled in the art the following test data are presented.
Three embodiments of the present invention were formed by coextrusion, irradiated and stretched (oriented) by application of internal air (bubble technique) in accordance with the teachings de-scribed above. That is, the five layer stretch/shrink films in accordance with the invention were produced by using four or five extruders feeding molten polymer into an annular die. The individual melt streams were brought together within the die and exited as a tube or tape. The six mil single wall tube was quenched with water as it passed over a forming shoe.
The tube was then collapsed and tracked through an irradiation unit where it received between seven and eight megarads dosage. The tape was then Z0 reheated in an EQ oven and biaxially oriented to between 3.0:1 and 3.4:1 in both the longitudinal and transverse directions. The film was double wound at the rack winder. These embodiments are hereinafter designated X, Y and Z.
Embodiment X was a five layered film irradiated with approximately 7-8 MR and had an approximate layer thickness ratio of 1jl.5/1/1.5/1.
Embodiment X comprised a layer structure of "A/B/C/B/A".
Embodiment Y was also a five layered film irradiated with approximately 7-8 MR and also had an approximate layer thickness ratio of 1/1.5/1/1.5/1. Embodiment Y also comprised a layer structure of "A/B/C/B/A".
- Embodiment Z was likewise a five layer film irradiated with approximately 7-8 MR with a layer thickness ratio like that of the em-bodiments X and Y. Embodiment Z comprises a layer structure of "C/B/C/B/C".
Il : ,' '' ." ' 1 3247~q In all of these examples A represents an ethylene vinyl acetate copolymer having from about 3.0% to about 3.6% vinyl acetate derived units (El Paso PE 204CS284); B represents a linear low density polyethylene having a density of about 0.920 gm/cm3 (Dowlex 2045.04) and C represents very low density polyethylene. In the case of embodiments X and Z, the particular VLDPE resin used was Dow XU61512-08L having a density of about .905 and a melt index of about .8 grams per 10 minutes. In the case of embodiment Y, the VLDPE resin used was DSM2H286 having a density of about .902 and a melt index of about 2.2.
Data with regard to a stretch/shrink film, recorded in U. S.
Patent No. 4,617,241 having similar layer thickness ratios is also pre-sented herewith for comparison with embodiments X, Y, and Z. This comparative example i9 designated "Comp. 1".
Table I, below, compares the four products with regard to several differing physical characteristics.
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The following footnotes apply to Table I.
1. ASTM D882-81 2. All values in Table I are averages obtained from four (4) replicate measurements.
3. C. L. Is Confidence Limit - for example, if the reported average value was 10 and the 95% C.L. was 2, then if 100 repllcate readings were made, 95 of them would have a value between 8 and 12, inclusive.
4. ASTM D882-81 5. ASTM D882-81 6. ASTM D2732-70 (reapproved 1976) It should be understood that the detailed description and specific examples which indicate the presently preferred embodiments of the invention are given by way of illustration only since various changes and modifications within the spirit and scope of the invention will become apparent to those of ordinary skill in the art upon review of the above detailed description and examples.
.
In view of the above:
;1~
FIELD OF TH~ INVENTION -The pre~ent invention relates to a heat shrinkable, thermoplastic packaging film. In particular, the invention provldes ln a multllayer thermoplastlc packaglng film havlng at least flve layer~, lncluding a layer o$ llnear low denslty polyethylene, the improvement whereinl (a) a core layer comprl~es a very low denslty polyethylene;
(b) lntermedlate layers adjacent each slde o$ the core layer comprise a linear low denslty polyethylene; and (c) two outer layers each bonded to a respective intermediate layer comprise a very low denslty polyethylene;
whereln the film has a modulus at 73F of less than about 17,000 pBi in the longitudinal and transverse directlon.
BACKGROUND O~ THE INVENTION
The preæent inventlon i8 dlrected to new and useful multllayer heat shrinkable film formulations. One dlstlngulshing ~- ~
feature of a shrink fllm i8 the film's ability, upon exposure to a ~ ;--certain temperature, to shrink, or, if restralned from shrlnking, to generate shrlnk tension within the film.
The manufacture of shrlnk fllms, as is well known in the art, may be generally a¢complished by extrusion (single layer ~-films) or coextrusion (multilayer films) of thermopla3tic resinous ;
material~ which have been heated to their flow or melting po~nt from an ex~rusion or coextrusion die in, for example, elther tubular or planar ~sheet) form. -~
`` 1 324749 After a post extrusion quenching to cool by, for example, the well-known cascading water method, the relatively thick "tape" extrudate is then reheated to a temperature within its orientation temperature range and stretched to orient or align the crystallites and/or molecules of the material. The orientation temperature range for a given material or materials will vary with the different resinous polymers and/or blends thereof which comprise the material. However, the orientation tempera-ture rang~ for a given thermoplastic material may generally be stated to be below the crystalline melting point of the material but above the second order transition temperature (sometimes referred to as the glass transition point) thereof. Within this temperature range it is easy to effectively orient the material.
The terms "orientation" or "oriented" are used herein to generally describe the process step and resultant product characteristics obtained by stretching and immediately cooling a resinous thermoplastic polymeric material which has been heated to a temperature within its orientation temperature range so as to revise the inter-molecular config-uration of the material by physical alignment of the crystallites and/or molecules of the material to improve certain mechanical properties of the film such as, for example, shr~nk tension and orientation release stress.
Both of these properties may be measured in accordance with ASTM D 2838-81. When the stretching force is applied in one direction uniaxial orientation results. When the stretching force is applied in two -directions biaxial orientation results. The term oriented is also herein used interchangeably with ~he term "heat shrinkable" with these terms de-signating a material which has been stretched and set by cooling while sub-stantially retaining its stretched dimensions. An oriented (i.e. heat I shrinkable) material will tend to return to its original unstretched (un-¦ extended) dimensions when heated to an appropriate elevated temperature.
Returning to the basic process for manufacturing the film as I discussed above, it can be seen that the film, once extruded (or ¦ coextruded if it is a multi-layer film) and initially cooled by, for example, cascading water quenching, is then reheated to within its orientation temperature range and oriented by stretching. The stretching ~2 .
to orient may be accomplished in many ways such as, for example, by "blown bubble" techniques or "tenter framing". These processes are well known to those in the art and refer to orientation procedures whereby the material is stretched in the cross or transverse direction (TD) and/or in the longitudinal or machine direction (MD). After being stretched, the film is quickly quenched while substantially retaining its stretched dimensions to rapidly cool the film and thus set or lock-in the oriented molecular configuration.
Of course, if a film having little or no orientation is de-sired, e.g. non-oriented or non-heat shrinkable film, the film may be formed from a non-orientable material or, if formed from an orientable material may be "hot blown". In forming a hot blown film the film i9 not cooled immediately after extrusion or coextrusion but rather is first stretched shortly after extrusion while the film is still at an elevated temperature above the orientation temperature range of the material.
Thereafter, the film is cooled, by well-known methods. Those of skill in the art are well familiar with this process and the fact that the result-ing film has substantially unoriented characteristics. Other methods for forming unoriented films are well known. Exemplary, is the method of cast extrusion or cast coextrusion which, likewise, is well known to those in the art.
After setting the stretch-oriented molecular configuration the film may then be stored in rolls and utilized to tightly package a wide variety of itemæ. In this regard, the product to be packaged may first be enclosed in the heat shrinkable material by heat sealing the shrink film to itself where neceæsary and appropriate to form a pouch or bag and then inserting the product therein. If the material was manufactured by "blown bubble" techniques the material may still be in tubular form or it may have been slit and opened up to form a sheet of film material.
Alternatively, a sheet of the material may be utilized to over-wrap the product. These packaging methods are all well known to those of skill in the art. Thereafter, the enclosed product may be subjected to elevated temperatures by, for example, passing the enclosed product through a hot air or hot water tunnel. This causes the enclosing film to shrink around the product to produce a tight wrapping that closely conforms to the ', ' "`,`"' - 1 3 2 4 ~ ~ 9 64536-630 contour of the product. As stated above, the fllm sheet or tube may be formed lnto bags or pouches and thereafter utllized to psckage a produc~.
In thls case, lf the film has been formed as 8 tube lt may be prefersble to first sllt the tubular fllm to form a fllm sheet and thereafter form the ~heet lneo bags or pouches. Such beg or pouch formlng methods, llkewlse, are well known to those of sklll in the art.
The above general outllne for manufacturlng of fllms 19 not meant to be all lncluslve slnce such processes are well known to those ln the art. For example, see U.S. Patent Nos. 4,274,900; 4,229,241;
4,194,039; 4,188,443; 4,048,428; 3,821,182 flnd 3,022,543. The dlsclo-sure6 of these patents are generally representatlve of such processes .
':
: : -Alternatlve methods oE produclng films of thls type are knownto those ln the art. One well-known alternative ls the methad of formlng 15 a multi-layer fllm by an extruslon coatlng rather than by an extruslon or ~ -coextruslon process as was di~cussed above. In extruslon coatlng a flrst tubular layer 1B extruded and thereafter sn addltlonal layer or layers ls sequentlally coated onto the outer surface of the flrst tubular layer or a successlve layer. Exemplary of thls method is U.S. Pat. No. 3,74l,253.
Thls patent 19 generally representatlve of an extruslon coating process.
, ' ' '' , ,, : ', ' Msny other process varlatlons for formlng fllms are well known l~ to those in the art. For example, multlple layers may be flrst ¦~ coextruded wlth addltlonsl layers thereafter belng extrusion coated - 25 thereon. Or two multl-layer tubes may be coextruded wlth one of the tubes thereafter belng extruslon coated or laminated onto the other. The extrusion coatlng method of film formation is prefer~ble to coextrudlng the entlre film when lt ls deslred to sub~ect one or more layers of the film to fl treatment which may be harmful to one or more of the other layers. Exe~plary of such a situation is a case where it 18 deslred to l~ irradlate one or more layers of a film contalnlng an oxygen barrler layer j comprised of one or more copolymers of vlnylldene chlorlde and vlnyl chlorlde. Those of sklll in the art generally recognlze that lrradlatlon l ls generaliy harmful to such oxygen barrler layer composltions. Accord-, ~
, ~ .
1 32474~
lngly, by means of extruslon coatlng, one may flrfit extrude or coextrude a flrst layer or layers, subJect that layer or layers to lrradlAtlon and thereafter extruslon cost the oxygen ~arrler layer and, for that matter, other layers sequentially onto the outer surface of the extruded prevl-ously lrradlated tube. Thls sequence allows for the lrradlatloncross-llnking of the flrst layer or layers wlthout sub~ectlng the oxygen barrier layer to the harmful effect~ thereof.
Irradlation of an entlre film or a layer or layers thereof may be deslred 80 as to lmprove the film's reslstance to abuse and/or puncture and other phy~lcal characterlstics. It 18 generally well known ln the art that lrradlatlon of certaln fllm materlals results ln the cross-llnklng of the polymerlc molecular chalns contained thereln and that such action generally results in a material having improved abuse re61stance.
Irradiatlon may be accompllshed by the use of hlgh energy electrons, ultra vlolet radiation, X-rays, gammA rsys, beta particles, etc. Prefersbly, electrons are employed up to about 20 megarads (MR) dosage level. The lrradlation source can be any electron beam generfltor operatlng in a range of about 150 kllovolts to about 6 megavolts wlth a power output capable of supplylng the desired dosage. The voltage can be ad~usted to approprlflte level~ whlch may be for example l,000,000 or 2,000,000 or 3,000,000 or 6,000,000 or higher or lower. Many apparatus for irradiatlng fllms are known to those of ~kill ln the art. The lrrndlatlon ls usually carrled out at a dosage between about 1 MR and about 20 MR, with a preferred dosage range of about 2 MR to about 12 MR. Irradlatlon can be carried out conveniently at room temperature, although higher and lower temperaturec, for exsmple, 0 ~o 60 may be employed.
: ' ':
Cross-linking may also be accompllshed chemlcally through utlllzation of peroxldes a~ is well known to those of sklll ln the art.
A general dlscu6slon of cross-llnklng can be found at pages 331 to 414 of volume 4 of the Encyclopedla of Polymer Sclence and Technology, Pl~stlc6, Reslns, Rubber~, Plber8 publlshed by John Wlley b Sons, Inc. and copy-rlghted ln 1966. Thi~ document has a Library of Congre~s Cfltalog Card Number of 64-22188- -,.. ,' ~
Another possible processing variation is the application of a fine mist of a silicone or anti-fog spray to the interior of the freshly extruded tubular material to improve the further processability of the tubular material. A method and apparatus for accomplishing such internal application is disclosed in U.S. Patent No. 4,612,245.
The polyolefin family of shrink films and, in particular, the polyethylene family of shrink films provide a wide range of physical and performance characteristics such as, for example, shrink force (the amount of force that a film exerts per unit area of its cross-section during shrinkage), the degree of free shrink (the reduction in linear dimension in a specified direction that a material undergoes when sub-jected to elevated temperatures while unrestrained), tensile strength (the highest force that can be applied to a unit area of film before it begins to tear apart), heat sealability, shrink temperature curve (the relation-ship of shrink to temperature), tear initiation and tear resistance (theforce at which a film will begin to tear and continue to tear), optics (gloss, haze and transparency of material), elongation (the degree the film will stretch or elongate at room temperature), elastic memory (the degree a film will return to its original unstretched (unelongated) dimension after having been elongated at room temperature), and dimen-sional stability (the ability of the film to retain its original dimensionæ under different types of storage conditions). Film charac-teristics play an lmportant role in the selection of a particular film and they differ for each type of packaging application and for each type of package. Consideration must be given to the product size, weight, shape, rigidity, number of product components and other packaging materi-i als which may be utilized along with the film material and the type of packaging equipment available.
' ~ In view of the many above-discussed physical characteristics i :~ 30 which are associated with polyolefin films and films containing a polyolefin constituent and in further view of the numerous applications with which these films have already been associated and those to which they may be applied in the future, it is readily discernable that the need for ever improving any or all of the above described physical characteristics or combinations thereof in these films is great, and, .' naturally, ongoing. In particular, the quest for a heat shrinkable polyethylene film having an improved combination of elongation, abuse resistance, and flexibility has been ongoing since such a film could compete well in the trayed product (for example, meat such as poultry parts) over-wrap market. Historically, polyvinyl chloride (PVC) films have beenutilized in this overwrap application because of their good degree of elongation and elastic memory. PVC was superior to conventional heat shrinkable films with regard to overwrapped trayed products which were subject to moisture loss because the PVC was elastic and continued to contract as the product lost moisture and shrank during the distribution cycle. The result was a tight package which was somewhat unattractive because it was leaky. The elasticity of PVC also allowed automatic over-wrapping machinery to stretch the PVC material about the trayed product during overwrapping of the product and the associated tray. In spite of the fact that the package was leaky, PVC proved superior to conventional heat shrink packages because such conventional packaging materials possessed relatively poor elasticity or elastic memory. Thus, when a product wrapped in such a material shrank from moisture loss during the distribution cycle the film did not also shrink and the result was a loose package having a shopworn appearance.
Unfortunately, PVC has several drawbacks associated therewith which those in the art wish to improve upon or wholly eliminate. Exem-I plary of these drawbacks is the fact that PVC tray overwrap film general-¦ ly evidences both (1) poor seal integrity and (2) poor abuse resistance.
.....
25The poor seal integrity of PVC overwrap films arises at least I in part from the fact that the PVC material in PVC overwrapped trays is j tack welded to itself as opposed to being hermetically sealed. Thus, the liquid purge or juices which exude from the overwrapped trayed meat products will leak through a tack sealed PVC overwrapped tray and result 130 in a package that is unsightly and messy from a consumer viewpoint. This ¦drawback appears to be irreconcilably linked to PVC since attempts to Ihermetically seal PVC in a commercial tray overwrap environment usually result in "burn-through" of the PVC material.
Il 7 , ,, . ; . , ~ ., . . , . - - . .. .. ~ . . , , . ., .. " . , , , . . . . . - ., .
. , ... . ., , . , . . .. ,. . - ; . ,, - ~. , ., .. ~ , Another maJor drawback of PVC tray overwrap materlal 19, AS
stated above, the material's poor reslstance to abuse. In this regard the PVC materlnl tends to tear along the edges of the overwrapped tray lf rubbed durlng tr~n~lt by another tray or ~n encloslng carton.
Past attempts to produce a heat shrlnkable polyolefln fllm whlch po~sesses 6atlsfactory elongatlon and elastic memory have resulted ln a fllm which 19 deflclent ln lts resis~ance to tear propagation. That is to say the fllm has the téndency to tear rapidly or "zlpper" once punctured. The "21pperlng" problem ls of great concern slnce thls tralt substantlally reduces the utllity of a fllm for nppllcations lnvolvlng automatlc packaglng equlpment. Zlppered fllm results ln increased down tlme. Heat shrlnkable polyolefln films havlng lmproved abuse resls- -tance are known to those ln the art. Recent developments include the fllm descrlbed ln U. S. Patent No. 4,617,241 whlch has provlded a satls-factory comblnatlon of deslred physlcal characterlstics ln that the fllm evldences a new and lmproved comblnatlon of phy~lcal characterlstlcs--e.g.
heat shrlnkablllty, elongatlon, elastic memory, heat sealablllty and abuse reslstance (puncture reslstance and reslstance to tear propagation).
However, as useful as these recent fllms have proven ln stretch/
shrink packaging appllcatlons, ln certaln appllcatlons lt 18 deslrable to provlde a multllayer fllm whlch ln some cases provides even better elonga-tlon characterlstics, lmproved abuse characterlstics, and a lower modulus (i.e. higher flexlblllty) film which wlll improve machlnablllty.
AIMS OF THE PRESENT INVENTION
, Accordlngly, the present invention seeks to provlde a trny overwrap polyolefin fllm that wlll be an lmprovement over the prior art tray overwrap fllms.
The present invention also seeks to provide a :.
polyolefln tray overwrap fllm havlng a deslred new and lmproved comblna-30 tion of phy8ical characterl8tlc8 such as, for example, abuse re~lstance, elongatlon and flexlblllty.
'~' .
64s36-63n The present invention also seeks to provide a five layer polyolefln fllm havlng an lnterlor core layer comprislng a very low denslty polyethylene; two ~dJacent lntermediate lnyers compri61ng a llne~r low den~lty polyetllylene and two outer layers comprising el~her an ethylene vinyl acetate copolymer or n very low density polyethylene.
The broad scope of applicability of the pre6ent invention wlll become apparent to tho6e of ordlnary 6klll ln the art from the detall6 dlsclo6ed herelnafter. However, lt should be understood that the followlng detalled descrlptlon whlch lndlcate6 several preferred embodlments of the present lnventlon ls only glven for purpo6es of lllustratlon slnce varlous changes and modlflcatlons well wlthln the ~cope of the present lnventlon wlll become apparent to tho6e of ordlnary ~klll ln the art ln vlew of the following detalled descrlption.
,,.--~.....
DEFINITIONS ;:~
"
Unless speclficslly set forth and defined or otherwise limited, the terms "polymer" or "polymer resin" a8 used herein generally lnclude`, but are not llmited to, homopolymers, copolymers, such as, for example block, graft, random and alternatlng copolymers, terpolymers etc. and blends and modlficstlons thereof. Furthermore, unles6 otherwlse speclfi-cslly llmlted the terms "polymer" or "polymer resln" shall lnclude all possible symmetrlcal structures of the materlsl. These structure6 lnclude, but are not llmlted to, lsotactic, syndlotactic flnd random ~ymmetrles.
.
The terms "melt flow" as uaed hereln or "melt flow lndex" ls the amount, ln grams, of a thermoplastlc re61n whlch can be forced through a given oriflce under a speclfied pre6sure and temperature wlthin ten minutes. The value 6hould be determined ln accordance wlth ASTM D
1230.
.' '. ' 404/ô70310/4/9 q '.. .
. .
- 1 32474q The terms "outer" or "outer layer" as used herein mean a layer of a multi-layer film which normally comprises a surface thereof in a five-layer embodiment or at least lies outside of the intermediate and core layers.
The term "core" or "core layer" as used herein usually refers to an interior layer of a multi-layer film having an odd number of layers wherein the same number of layers is present on either side of the core layer. In films having an even number of layers, the core layer can be either of the two central layers.
The term "intermediate" or "intermediate layer" as used herein refers to an interior layer of a multi-layer film which is positioned between a core layer and an outer layer of said film.
The term polyolefin as used herein refers to polymers of relatively simple olefins such as, for example, ethylene, propylene, butenes, isoprenes and pentenes; including, but not limited to, homopolymers, copolymers, blends and modifications of such relatively simple olefins.
The term "polyethylene" as used herein refers to a famlly of resins obtalned by polymerizing the gas ethylene, C2H4. By varying the catalysts and methods of polymerization, properties such as density, melt index, crystallinity, degree of branching and cross-linking, molecular weight and molecular weight distribution can be regulated over wide 1 ranges. Further modifications are obtained by copolymerization, chlori-¦ nation, and compounding additives. Low molecular weight polymers of i~ 25 ethylene are fluids used as lubricants; medium weight polymers are waxes ¦ miscible with paraffin; and the high molecular weight polymers (generally i over 6,000) are resins generally used in the plastics industry. Polyeth-~ ylenes having densities ranging from about 0.900 g/cc to about 0.940 g/cc i are called low density polyethylenes while those having densities from 1 30 about 0.941 g/cc to about 0.965 g/cc and over are called high density¦ polyethylenes. The low density types of polyethylenes are usually polymerized at high pressures and temperatures whereas the high density types are usually polymerized at relatively low temperatures and pressures.
!
1 3247~9 The term "linear low density polyethylene" (LLDPE) as used herein refers to copolymers of ethylene with one or more comonomers selected from C4 to C10 alpha olefins such as butene-l, octene, etc. in which the molecules thereof comprise long chains with few side chains branches or cross-linked structures. The side branching which is present will be short as compared to non-linear polyethylenes. Linear low density polyethylene has a density usua]ly in the range of from about 0.916 g/cc to 0.940 g/cc for film making purposes. The melt flow index of linear low density polyethylene generally ranges from between about 0.1 to about 10 grams per ten minutes and preferably between from about 0.5 to about 3.0 grams per ten minutes. Linear low density polyethylene resins of this type are commercially available and are manufactured in low pressure vapor phase and liquid phase processes using transition metal catalysts.
The term "very low density polyethylene" (VLDPE) is used herein to describe a linear ethylene-alpha-olefin copolymer having densities of generally between 0.890 and O.91S grams/cubic centimeter, and produced by cataly~ic, low pressure processes.
The term "ethylene vinyl acetate copolymer" (EVA) as used herein refers to a copolymer formed from ethylene and vinyl acetate monomers wherein the ethylene derived units in the copolymer are present in ma;or amounts and the vinyl acetate derived units in the copolymer are present in minor amounts.
An "oriented" or "heat shrinkable" material is defined herein as a material which, when heated to an appropriate temperature above room temperature ~for example 96C), will have a free shrink of 5% or greater in at least one linear direction.
All compositional percentages used herein are calculated on a "by weight" basis. `
Free shrink should be measured in accordance with ASTM D 2732.
..
The elongation properties of the film should be measured in accordance with ASTM D 638.
~` :
5~
A "cross-llnked" materlal as used herein shall be deflned as a materlal whlch after refluxlng ln bolllng toluene or xylene, as approprlate, for forty (40~ hours shall have a welght percent residue of at least 5 percent. A procedure for determlnlng whether a materlal ls cross-llnked vel non is to reflux 0.4 gram of the materlal ln bolllng toluene or another approprlate solvent, for example xylene, for twenty (20) hours.
If no lnsoluble resldue (gel) remalns the materlal ls determlned not to be cross-llnked. If, after twenty (20) hours of refluxlng lnsoluble resldue (gel) remalns the materlal is refluxed under the same condltlons for another twenty (20) hours. If more than 5 welght percent of the materlal remalns upon concluslon of the ~econd refluxlng the materlal ls consldered to be cross-linked.
¦ Preferably, at least two repllcates are utlllzed.
j A rad ls the quantlty of lonlzlng radlatlon that results ¦ ln the absorptlon of 100 ergs of energy per gram of a radlated -materlal, regardless of the source of the radiatlon. A megarad 19 ~ 106 rads. (MR ls an abbrevlatlon for megarad).
¦ SUMMARY OF THE INVENTION
It has been dlscoverd that a flexlble, heat shrlnkable thermoplastlc packaglng fllm havlng a deslrable comblnatlon of physlcal characterlstlcs such as, elongatlon, abuse reslstance, flexlblllty, and heat shrlnkablllty has been achleved by the multllayer flexlble, thermoplastlc packaglng film of the present lnventlon. This multllayer fllm comprlses a core layer comprislng ;~
,' " - .
`'.':
1 32474~
very low density polyethylene, intermediate layers adjacent each -~
~lde of the core layer compri~iing a linear low denslty polyethylene, and two outer layers each bonded to a respectlve intermediate layer, and compri~iing very low denslty polyethylene.
Preferably, the multilayer fllm is both orlented and lrradlated.
Preferably the $ilm has a modulus of less than about 17,000 p8i ln the longltudinal direction and les~ than about 13,000 psi in the transverse dlrectlon. A1BO preferably the elongation of the film at break at 73F loi at least about 220% ln the longltudlnal dlrectlon and at lea~t about 250% in the tran~verse dlrectlon.
12a 1 32474q BRIEF DESCRIPTION OF THE DRAWING
Figure I is a cross-sectional view of a preferred five layered embodiment of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring to Figure I, which is a cross-sectional view of a five layered preferred embodiment of the present invention, it is seen that this embodiment comprises a core layer 1, two ad~acent intermediate layers 2 and 3 and two skin or surface layers 4 and 5. The preferred thickness ratio of the five layers of 1/1.5/1/1.5/1 is demonstrated in Figure I. A preferred core layer 1 formulation comprises very low density polyethylene.
' ' .
Our experimentation has revealed an especially preferred core layer formulation is very low density polyethylene which may be obtained from Dow Chemical Company under the trade designation XU61512.08L. This resin is believed to have a density at 23C of about 0.905 gm/cm3 and a melt flow rate (measured by condition E) of about .8 gm/10 min. Other very low den~ity polyethylenes may be utilized to form the core layer 1, for example DSM 2H286 available from Dutch State Mines.
'~
Returning to Figure I, and in particular, ad~acent intermediate layers 2 and 3 it has been determined that a preferred intermediate layer formulation should comprise a linear low density polyethylene material.
A preferred linear low density polyethylene is Dowlex 2045.04. Other linear low tensity polyethylene materials or blends of two or more linear low density polyethylene materials may be utilized to form the intermediate layers 2 and 3. Preferably the composition of intermediate lay0rs 2 and 3 is the same, however, different linear low density polyethylenes or - blends thereof may be utilized for each intermediate layer. Dowlex 2045.04 is believed to have a density of about 0.920 gm/cm3 and a flow rate ~measured by condition E) of from about 0.7 to 1.2 gm/ten minutes.
..
~, . .
With rega~d to outer layers 4 and 5 it has been determined that a preferred skin layer formulation comprises either a copolymer of ethylene and vinyl acetate, or very low density polyethylene. VLDPE utilized to form the core layer 1 may, preferably, be the same material as that which is utilized to form the two outer layers 4 and 5. A particularly preferred outer layer ethylene vinyl acetate copolymer is PE204CS284. This resin is available ~rom El Paso Polyolefins Company, and is believed to have a density at 23C of from about 0.9232 grams/cubic centimeter to about 0.9250 grams/cubic centimeter and a melt flow rate (measured by condition E) of about 2.0 grams/10 minutes. Other ethylene vinyl acetate copolymers or blends of two or more ethylene vinyl acetate copolymers may be utilized to form outer layers 4 and 5. Preferably the composition of outer layers 4 and 5 is the same, however, different VLDPE resins or blends thereof, and different ethylene vinyl acetate copolymers or blends thereof, may be utilized for each outer layer.
Those skilled in the art will ~eadily recognize that all of the above disclosed, by weight, percentages are subject to slight variation.
Additionally, these percentages may vary slightly as a result of the inclusion or application of additives such as the silicone mist discussed above or agents such as slip and anti-block agents. A preferred anti-block agent is silica which is available from Johns Manville under the trade-name White Mist. Preferred slip agents are erucamide (available ' from Humko Chemical under the trade-name Kemamide E), and stearamide ¦ (available from the Humko Chemical Company under the trade-name Kemamide S) and N, N-' dioleoylethylenediamine (available from Glyco Chemical under the trade-name Acrawax C). A preferred silicone spray is a liquid polyorganosiloxane manufactured by General Electric under the trade designation General Electric SF18 polydimethylsiloxane.
The general ranges for inclusion or, in the case of the 1 30 silicone spray, the application of these additives are as follows:
; (1) silica: 250-3000 ppm (2) N, N-' dioleoylethylenediamine: 200-4000 ppm (3) erucamide: 200-5000 ppm (4) stearamide: 200-5000 ppm (5) silicone spray: 0.5 mg.ft2-and up 1~ .
When utilized within the specification and claims of the present application the term "consisting essentially of" is not meant to exclude slight percentage variations or additives and agents of this sort.
Additional layers and/or minor amounts of additives of the types described above may be added to the film structure of the present invention as desired but care must be taken not to adversely affect the desirable physical properties and other characteristics of the inven-tive film.
In the preferred process for making the multi-layer film of the present invention the basic steps are coextruding the layers to form a multilayer f ilm, irradiating the f ilm, and then stretching the f ilm to biaxially orient. These steps and additional desirable steps will be explained in detail in the paragraphs which follow.
The process begins by blending, if necessary, the raw materials (i.e. polymeric resins) in the proportions and ranges desired as dis-cussed above. The resins are usually purchased from a supplier in pellet form and can be blended in any one of a number of commercially available blenders as is well known in the art. During the blending process any additives and/or agents which are desired to be utilized are also incorporated.
The resins and applicable additives and/or agents are then fed to the hoppers of extruders which~--feed a coextrusion die. For the preferred five-layer film having two identical outer layers and two identical intermediate layers at least 3 extruders need to be employed, one for the two outer layers, one for the two intermediate layers and one for the core layer. Additional extruders may be employed if a film having non-identical outer layers or non-identical intermediate layers is desired.
The materials are coextruded as a relatively thick tube or "tape" which has an initial diameter dependent upon the diameter of the coextrusion die. The final diameter of the tubular film is dependent upon the racking ratio, e.g.
the stretching ratio. Circular coextrusion dies are well known to tho~e in the art and can be purchased from a number of manufacturers. In addition to 404/870310/4/15 -~
,: ~
-:: 1 3247~q tubular coextrusion, slot dies could be used to coextrude the material in sheet form. Well known single or multi-layer extrusion coating processes could also be utilized, if desired.
:
An additional process step which should be utilized to manufac-ture the preferred embodiment of the presently inventive film is to irradiate the tape or unexpanded tubing or sheet by bombarding it with high-energy electrons from an accelerator to cross-link the materials of ¦ the tube. Cross-linking greatly increases the structural strength of the I film or the force at which the material can be stretched before tearing! lo apart when the film materials are predominately ethylene such as polyeth-ylene or ethylene vinyl acetate. Irradiation also improves the optical properties of the film and changes the properties of the film at higher temperatures. A preferred irradiation dosage level is in the range of from about 0.5 MR to about 12.0 MR. An even more preferred range is from about 4 MR to about 8 MR. The most preferred dosage level is approximately 7 to 8 MR.
~i Following coextrusion, quenching to cool and solidify, and irradiation of the tape, the extruded tape is reheated and inflated into a bubble by application of internal air pressure thereby transforming the narrow tape with thick walls into a wide film with thin walls of the desir-ed film thickness and width. This process is sometimes referred to as the "trapped bubble technique" of orientation or as "racking". The degree of inflation and subsequent stretching is often referred to as the "racking ratio" or "stretching ratio". For example, a transverse racking or stretch-ing ratio of 2.0 would mean that the film had been stretched 2.0 times itsoriginal extruded size in the transverse direction during transverse rack-ing. After stretching, the tubular film is then collapsed into a super-imposed lay-flat configuration and wound into rolls often referred to as "mill rolls". The racking process orients the film by stretching it trans-versely and longitudinally and thus imparts shrink capabilities to the film.Additional longitudinal or machine direction racking or stretching may be accomplished by revolving the deflate rollers which aid in the collapsing of the "blown bubble" at a greater speed than that of the rollers which serve to transport the reheated "tape" to the racking or blown bubble area.
~ ':
3~ 404/870310/4/16 li r,~" .~ ; . - . . ',. '.'. " . ' : . . ' ' .
Preferred transverse and longitudinal stretching ratios of the present film range from between about 2.5 trans-verse by about 3.0 longitudinal to about 5.0 transverse and about 5.0 longitudinal. A particularly preferred stretching ratio is about 3.0 to 4.0 transverse by about 3.0 to 4.0 longitudinal. All of these methods of orientation are well known to those of skill in the art.
To further disclose and clarify the scope of the present invention to those skilled in the art the following test data are presented.
Three embodiments of the present invention were formed by coextrusion, irradiated and stretched (oriented) by application of internal air (bubble technique) in accordance with the teachings de-scribed above. That is, the five layer stretch/shrink films in accordance with the invention were produced by using four or five extruders feeding molten polymer into an annular die. The individual melt streams were brought together within the die and exited as a tube or tape. The six mil single wall tube was quenched with water as it passed over a forming shoe.
The tube was then collapsed and tracked through an irradiation unit where it received between seven and eight megarads dosage. The tape was then Z0 reheated in an EQ oven and biaxially oriented to between 3.0:1 and 3.4:1 in both the longitudinal and transverse directions. The film was double wound at the rack winder. These embodiments are hereinafter designated X, Y and Z.
Embodiment X was a five layered film irradiated with approximately 7-8 MR and had an approximate layer thickness ratio of 1jl.5/1/1.5/1.
Embodiment X comprised a layer structure of "A/B/C/B/A".
Embodiment Y was also a five layered film irradiated with approximately 7-8 MR and also had an approximate layer thickness ratio of 1/1.5/1/1.5/1. Embodiment Y also comprised a layer structure of "A/B/C/B/A".
- Embodiment Z was likewise a five layer film irradiated with approximately 7-8 MR with a layer thickness ratio like that of the em-bodiments X and Y. Embodiment Z comprises a layer structure of "C/B/C/B/C".
Il : ,' '' ." ' 1 3247~q In all of these examples A represents an ethylene vinyl acetate copolymer having from about 3.0% to about 3.6% vinyl acetate derived units (El Paso PE 204CS284); B represents a linear low density polyethylene having a density of about 0.920 gm/cm3 (Dowlex 2045.04) and C represents very low density polyethylene. In the case of embodiments X and Z, the particular VLDPE resin used was Dow XU61512-08L having a density of about .905 and a melt index of about .8 grams per 10 minutes. In the case of embodiment Y, the VLDPE resin used was DSM2H286 having a density of about .902 and a melt index of about 2.2.
Data with regard to a stretch/shrink film, recorded in U. S.
Patent No. 4,617,241 having similar layer thickness ratios is also pre-sented herewith for comparison with embodiments X, Y, and Z. This comparative example i9 designated "Comp. 1".
Table I, below, compares the four products with regard to several differing physical characteristics.
.... . .. .. .. ..... . .. .. . .. ..... ..
: 1 324749 _ O O OO O O ~OD ~ ~ ~ O '' o o oo o o o o ~ ~ . .
~c x x ~q ~ x It~ ~ ~ ,` ~ o O ~ ~ ~ ~ ~D
, ~
, .
o o oo o o o ~ ~ ~ o~
o o oo o o X X X~ X
~, , , . . ....
O O O O o o1`_ ~
o o o o o o. . . . . . ..
, ~ ~ ~ ~ ~ ~X ~ ~ ~ X ~ . ,.
X X X X X X
, ~ ~ X
. .-.~ .
, . . .
,. ~.
o o oo o o _a~
~ H O O OO O O
~ :~q x x xx x x a~
,~ 1 _~ o i~
H
~ ~ . .
~: ~ `d': -' :- ~ ,' ~:~ ¢ sD O
, , ~ ~
: ~ . p . ~ ¢ P P o~ ' .
a~~o ~ ~0 a~ ~ .~1 ,-1 tq ~ ~ :
8 ~ ~ ~ 0 ~ ~ ~o ~ -E~~ ~ ~ O
cn oo ¢ ~ ~ ¢ : 3 `-: ::
19 `----`` 1 324749 o o o o o o oooooo o o o o o o o XX X X Xi-~
C~ ~~ o _ _ ~ a~ ~
C~l o o o o o o o o o o o o o o o o o o , X i~c X X X X
I` o~ n ~ ~ ~ ' ' ~o o ~ ~
o o o o o o o o o o o o X ~ X X # X
~ Ul X ~ ~
C~ o o ~ o ~-~ ~
~ o o o o8 8 g ~
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,~ ~ xx x x x x ~ J _ o ~;~
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.
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.
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f .~,~Yf ~ ? ~ r,~ ' ,r~ "~ ?~?
The following footnotes apply to Table I.
1. ASTM D882-81 2. All values in Table I are averages obtained from four (4) replicate measurements.
3. C. L. Is Confidence Limit - for example, if the reported average value was 10 and the 95% C.L. was 2, then if 100 repllcate readings were made, 95 of them would have a value between 8 and 12, inclusive.
4. ASTM D882-81 5. ASTM D882-81 6. ASTM D2732-70 (reapproved 1976) It should be understood that the detailed description and specific examples which indicate the presently preferred embodiments of the invention are given by way of illustration only since various changes and modifications within the spirit and scope of the invention will become apparent to those of ordinary skill in the art upon review of the above detailed description and examples.
.
In view of the above:
;1~
Claims (4)
1. In a multilayer thermoplastic packaging film having at least five layers, including a layer of linear low density polyethylene, the improvement wherein:
(a) a core layer comprises a very low density polyethylene;
(b) intermediate layers adjacent each side of the core layer comprise a linear low density polyethylene; and (c) two outer layers each bonded to a respective intermediate layer comprise a very low density polyethylene;
wherein the film has a modulus at 73°F of less than about 17,000 psi in the longitudinal and transverse direction.
(a) a core layer comprises a very low density polyethylene;
(b) intermediate layers adjacent each side of the core layer comprise a linear low density polyethylene; and (c) two outer layers each bonded to a respective intermediate layer comprise a very low density polyethylene;
wherein the film has a modulus at 73°F of less than about 17,000 psi in the longitudinal and transverse direction.
2. The film of claim 1 wherein each layer is cross-linked.
3. The film of claim 1 having a modulus of less than about 17,000 psi in the longitudinal direction and less than about 13,000 psi in the transverse direction.
4. The film of claim 1 having an elongation, at break at 73°F of at least about 220% in the longitudinal direction and about 250% in the transverse direction.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3675087A | 1987-04-10 | 1987-04-10 | |
| US036,750 | 1987-04-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1324749C true CA1324749C (en) | 1993-11-30 |
Family
ID=21890425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000553184A Expired - Fee Related CA1324749C (en) | 1987-04-10 | 1987-12-01 | Flexible stretch/shrink film |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4927708A (en) |
| EP (1) | EP0286430B1 (en) |
| JP (1) | JP2634628B2 (en) |
| AT (1) | ATE107224T1 (en) |
| AU (1) | AU597166B2 (en) |
| BR (1) | BR8801686A (en) |
| CA (1) | CA1324749C (en) |
| DE (1) | DE3850168T2 (en) |
| ES (1) | ES2054800T3 (en) |
| MX (1) | MX169269B (en) |
| NZ (1) | NZ223877A (en) |
| ZA (1) | ZA881918B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4952451A (en) * | 1988-11-17 | 1990-08-28 | W. R. Grace & Co.-Conn. | Stretch/shrink film with improved oxygen transmission |
| US4891253A (en) * | 1988-11-17 | 1990-01-02 | W. R. Grace & Co.-Conn. | Moisture barrier medical film |
| NZ226983A (en) * | 1988-11-17 | 1990-08-28 | Grace W R Nz | Multilayer heat shrink film comprising ethylene/vinyl acetate copolymer and very low density polyethylene polymer layers |
| GB8914703D0 (en) * | 1989-06-27 | 1989-08-16 | Dow Europ Sa | Bioriented film |
| US5234731A (en) * | 1990-05-25 | 1993-08-10 | W.R. Grace & Co.-Conn. | Thermoplastic multi-layer packaging film and bags made therefrom having two layers of very low density polyethylene |
| US5272236A (en) * | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| CA2048296C (en) * | 1990-08-13 | 2002-09-24 | Henry G. Schirmer | Blends of polypropylene and ethylene copolymer and films made from the blend |
| JP2960519B2 (en) * | 1990-10-09 | 1999-10-06 | 株式会社細川洋行 | Barrier infusion packaging material |
| US5089321A (en) * | 1991-01-10 | 1992-02-18 | The Dow Chemical Company | Multilayer polyolefinic film structures having improved heat seal characteristics |
| US5851610A (en) * | 1991-02-07 | 1998-12-22 | Applied Extrusion Technologies, Inc. | Shrink films and articles including the same |
| JP2648404B2 (en) * | 1991-04-10 | 1997-08-27 | 出光石油化学株式会社 | Polyethylene-based multilayer stretched film |
| US5288531A (en) * | 1991-08-09 | 1994-02-22 | The Dow Chemical Company | Pouch for packaging flowable materials |
| US5562958A (en) * | 1991-10-15 | 1996-10-08 | The Dow Chemical Company | Packaging and wrapping film |
| US5525695A (en) * | 1991-10-15 | 1996-06-11 | The Dow Chemical Company | Elastic linear interpolymers |
| US5395471A (en) | 1991-10-15 | 1995-03-07 | The Dow Chemical Company | High drawdown extrusion process with greater resistance to draw resonance |
| US5582923A (en) | 1991-10-15 | 1996-12-10 | The Dow Chemical Company | Extrusion compositions having high drawdown and substantially reduced neck-in |
| US5674342A (en) | 1991-10-15 | 1997-10-07 | The Dow Chemical Company | High drawdown extrusion composition and process |
| US5635286A (en) * | 1991-11-12 | 1997-06-03 | Kohjin Co., Ltd. | Heat shrinkable polyethylene laminate film |
| DK0544098T3 (en) * | 1991-11-27 | 1999-05-17 | Mitsubishi Chem Corp | Polyolefin-based packaging foil |
| US5935681A (en) * | 1992-10-30 | 1999-08-10 | Paulett; Harry K. | Perforated stretch wrap film |
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| JPS60105541A (en) * | 1983-11-14 | 1985-06-11 | 出光石油化学株式会社 | Multilayer film |
| US4617241A (en) * | 1984-01-23 | 1986-10-14 | W. R. Grace & Co., Cryovac Div. | Linear polyethylene stretch/shrink films |
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| US4514465A (en) * | 1984-05-30 | 1985-04-30 | W. R. Grace & Co., Cryovac Div. | Storm window film comprising at least five layers |
| US4640856A (en) * | 1985-04-29 | 1987-02-03 | W. R. Grace & Co., Cryovac Div. | Multi-layer packaging film and receptacles made therefrom |
| US4671987A (en) * | 1986-04-07 | 1987-06-09 | El Paso Products Company | Printable composite stretch wrap film |
| US4778699A (en) * | 1986-09-15 | 1988-10-18 | Reynolds Metals Company | Plastics film laminates |
-
1987
- 1987-12-01 CA CA000553184A patent/CA1324749C/en not_active Expired - Fee Related
-
1988
- 1988-03-15 NZ NZ223877A patent/NZ223877A/en unknown
- 1988-03-17 ZA ZA881918A patent/ZA881918B/en unknown
- 1988-03-28 MX MX010910A patent/MX169269B/en unknown
- 1988-04-07 JP JP63084211A patent/JP2634628B2/en not_active Expired - Lifetime
- 1988-04-08 ES ES88303168T patent/ES2054800T3/en not_active Expired - Lifetime
- 1988-04-08 EP EP88303168A patent/EP0286430B1/en not_active Expired - Lifetime
- 1988-04-08 DE DE3850168T patent/DE3850168T2/en not_active Expired - Fee Related
- 1988-04-08 BR BR8801686A patent/BR8801686A/en unknown
- 1988-04-08 AT AT88303168T patent/ATE107224T1/en not_active IP Right Cessation
- 1988-04-08 AU AU14451/88A patent/AU597166B2/en not_active Ceased
- 1988-07-26 US US07/225,588 patent/US4927708A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NZ223877A (en) | 1990-06-26 |
| EP0286430B1 (en) | 1994-06-15 |
| AU1445188A (en) | 1988-10-13 |
| ES2054800T3 (en) | 1994-08-16 |
| US4927708A (en) | 1990-05-22 |
| BR8801686A (en) | 1988-11-16 |
| EP0286430A3 (en) | 1989-05-03 |
| ZA881918B (en) | 1988-09-09 |
| JP2634628B2 (en) | 1997-07-30 |
| JPS63264349A (en) | 1988-11-01 |
| AU597166B2 (en) | 1990-05-24 |
| MX169269B (en) | 1993-06-28 |
| EP0286430A2 (en) | 1988-10-12 |
| DE3850168T2 (en) | 1994-09-22 |
| ATE107224T1 (en) | 1994-07-15 |
| DE3850168D1 (en) | 1994-07-21 |
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