CA2085622C

CA2085622C - Coated abrasive article and method of making same

Info

Publication number: CA2085622C
Application number: CA002085622A
Authority: CA
Inventors: Walter L. Harmer; Robert J. Devoe; Erick G. Larson; Don H. Kincaid; Peggy S. Willett; Jerry W. Williams
Original assignee: Minnesota Mining and Manufacturing Co
Current assignee: 3M Co
Priority date: 1992-01-22
Filing date: 1992-12-17
Publication date: 2004-11-02
Anticipated expiration: 2012-12-17
Also published as: ZA9210123B; DE69320497D1; AU657588B2; KR930016521A; BR9300231A; ES2120455T3; US5360462A; CA2085622A1; RU2106953C1; CN1074705C; EP0552782B1; KR100249979B1; EP0552782A1; JP3441752B2; US5256170A; JPH05247234A; CN1074637A; DE69320497T2; AU3036992A

Abstract

A method for preparing a coated abrasive article wherein the a plurality of abrasive grains are applied to a make coat such that the abrasive grains are substantially a mono-layer. The make coat precursor is a pressure-sensitive adhesive-like or pressure-sensitive adhesive. The make coat precursor is partially cured to approximate a pressure-sensitive adhesive-like layer or when fully cured is a pressure-sensitive adhesive. The make coat precursor has sufficient "tack" to hold the abrasive grains during the application and curing of the size coat, resulting in a substantially monolayer of abrasive grains.

Description

~ ~ j~ ?.. fi cT ~.'~y w,;,. ~.3 ~.' ~1.~ ::~ 4..d COATED. ABRASIVE ARTICLE AND
S METHOD OF MAKING SAME
BACKGROUND OF TIDE INDENTION
1. Field of the Invention This invention relates to a coated abrasive article and a method of making the coated abrasive article, and in particular to a method wherein the make coat precursor is at least partially cured before the abrasive grains are applied.

2. Description of the Related Art Coated abrasives generally comprise a flexible backing upon which a binder holds and supports a coating of abrasive grains. The coated abrasive typically employs a "make" coat precursor of resinous binder material. The make coat secures the abrasive grains to the backing. A "size" coat precursor of resinous binder material is applied over the make coat and abrasive grains. The size coat firmly bonds the abrasive grains to the backing. Additionally, the abrasive grains are generally oriented with their longest dimension perpendicular to the backing to provide an optimum cut rate.
In a typical manufacturing process for making coated abrasives, the make coat precursor is first applied to the backing. This is followed by electrostatic projection of the abrasive grains into the make coat precursor. The make coat precursor is then partially cured in order to set the abrasive grains. Next, the size coat precursor is applied over the abrasive grains. Finally, the make coat precursor and size coat precursor are fully cured.
One of the major problems associated with this process, is the tendency to apply multiple layers of abrasive grains during the electrostatic coating.
This is particularly true in the "fme" grades, that is, where the average particle size of the abrasive grain is less than about 150 micrometers, and usually less than about micrometers. In some instances there may be up to seven layers of abrasive grains applied. This multiple layer becomes increasingly a problem as the abrasive grain particle size is decreased. Reducing the coating weight of the abrasive grain tends to result in a blotchy, non-uniform type coating of multiple layers.
There are a number of disadvantages associated with the multiple layers of abrasive grains. The abrasive grains tend not to be ideally oriented and the abrasive grains tend to lay on top of one another. This results in reduced abrading performance. The multiple layers of abrasive grains can in some cases, reduce the flexibility of the product. Furthermore, the multiple layers of abrasive grains decrease cost efficiency of the coated abrasive due to the extra layers of abrasive grains.
U.S. Patent No. 2,015,658 (Bezzenberger) describes a method to avoid multiple layer phenomena when forming abrasive articles. The abrasive grain is applied to the make coat precursor by means of a metered roll.
U.S. Patent No. 2,053,360 (Benner et al.) describes a method of making a coated abrasive wherein the abrasive grains are sprinkled onto a nontacky film of a plasticizable binder. The film is then plasticized such that the binder wets the surface of the abrasive grain.
U.S. Patent No. 4,047,903 (Hesse et al.) describes a radiation curable binder comprising a resin prepared by at least a partial reaction of (a) epoxy monomers having at least 2 epoxy groups, for example, from diphenyIolproparie and epichlorohydrin, with (b) unsaturated monocarboxylic acids, and (c) optionally, polycarboxylic acid anhydride.
U.S. Patent No. 4,588,419 (Gaul et al.) describes an adhesive for coated abrasives comprising a mixture of (a) an electron beam radiation curable resin system comprising an oligomer selected from the group consisting of urethane acrylates and epoxy acrylates, a filler and a diluent, and (b) a thermally curable resin selected from the group consisting of phenolic resins, melamine resins, amino resins, alkyd resins, and furan resins.
U.S. Patent No. 4,751,138 (Tumey et al.) describes a coated abrasive in which either the make coat or the size coat comprises an ethylenically unsaturated . compound, an epoxy monomer and a photoinitiator.

U.S. Patent No. 4,927,431 (Buchanan et al.) describes an adhesive for coated abrasives comprising a mixture of (a) a radiation curable monomer selected from the group consisting of isocyanurate derivatives having at least one terminal or pendant acrylate group, isocyanate derivatives having at least one terminal or pendant acrylate group, and multifunctional acrylates having on average at least three pendant acrylate groups, and (b) a thermally curable resin selected from the group consisting of phenolic resins, epoxy monomers, urea-formaldehyde resins, melamine-formaldehyde resins, and polyamide resins.
U.S. Patent 4,985,340 (Plazzotto et al.) describes a polymeric precursor that can be employed as a binder for abrasive articles. The polymeric precursor is selected from the group consisting of (1) at least one thylenically unsaturated monomer, optionally, in combination with an epoxy monomer or polyurethane precursor, (2) at least one epoxy monomer, or (3) polyurethane precursors, and a curing agent comprising an organometallic salt and an onium salt.
U.S. Patent No. 4,997,717 (Rembold) describes a process for preparing a coated abrasive by applying a binder layer to a support, briefly irradiating the binder layer with actinic light, and then applying abrasive grain to the still tacky layer before or after irradiation, and subsequent or simultaneous heat curing.
SUMMARY OF THE INVENTION
Briefly, in one aspect of the present invention a coated abrasive article is provided comprising (1) a backing, (2) a make coat layer, wherein the make coat layer comprises (a) an ethylenically unsaturated monomer, (b) a -3a-cationically polymerizable monomer or a polyurethane precursor, and (c) a curing agent comprising (i) at least one organometallic complex salt, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt, and (iii) optionally, at least one free radical initiator, (3) a plurality of abrasive grains and (4) a size coat layer.
According to another aspect of the present invention, there is provided a coated abrasive article comprising: (1) a backing; (2) a make coat layer on one surface of the backing, wherein the make coat layer comprises the polymerized product of: (a) at least one thylenically unsaturated monomer, (b) at least one cationically polymerizable monomer, (c) at least one organometallic complex salt, and (d) at least one thermally decomposable ester reaction product of a tertiary alcohol and an acid that forms a chelation complex with the metal ion of the organometallic salt; (3) a plurality of abrasive grains on the surface or partially embedded into the surface of the make coat layer; and (4) a size coat layer coated over the plurality of abrasive grains and the make coat layer.
According to still another aspect of the present invention, there is provided a coated abrasive article comprising: (1) a backing; (2) a make coat layer on one surface of the backing, wherein the make coat layer comprises the polymerized product of: (a) at least one ethylenically unsaturated monomer, (b) a polyurethane precursor, wherein when cured, the polyurethane has a glass -3b-transition temperature above room temperature; (c) a polyurethane precursor initiator, and (3) a plurality of abrasive grains on the surface or partially embedded into the surface of the make coat layer; and (4) a size coat layer coated over the plurality of abrasive grains and the make coat layer.
In yet another aspect of the present invention, a first method is provided for making a coated abrasive article comprising:

(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises:
(a) at least one ethylenically unsaturated monomer, and (b) at least one of a canonically polymerizable monomer or a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
(i) at least one cationically polymerizable monomer or polyurethane precursor initiator, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelanon complex with the metal ion of the organometallic complex salt, provided that component (b) is a cationically polymerizable monomer, and (iii) optionally, at Ieast one free radical initiator;
(2) exposing the make coat precursor to an energy source to activate the organometallic complex salt;
(3) partially polymerizing, either sequentially or simultaneously, the canonically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer; or both;

(4) applying a plurality of abrasive grains into the make coat precursor;
(S) applying a size coat precursor;
(6) fully curing the make coat precursor; and (7) fully curing the size coat precursor.
When practicing the first method, it is preferable that steps 1 through 4 be accomplished in the order as written. Partial polymerization of (a) the canonically polymerizable monomer or the polyurethane precursor, or (b) the ethylenically unsaturated monomer, or both (a) and (b), results in a solid tacky, pressure-sensitive adhesive-like layer. Advantageously, the partially polymerized make coat does not flow and wet-up the sides of the abrasive grains and permits .a "smooth, °' evenly-coated, substantially mono-layer of abrasive grains. It is an another advantage of the present invention that steps 5 and 6 may be accomplished in any order, and that the order of steps 5 and 6 as written is merely one of a number of routes that may be utilized in practicing the present invention. When the ~,.n 40 ~y :,~j ~J 2~
- S -ethylenically unsaturated monomer is initiated by the application of electron beam irradiation, a free radical initiator is not required. In other instances, the ethylenically unsaturated monomer is initiated by adding a catalytically-effective amount of at least one free radical initiator.
In yet another aspect of the present invention, a second method is provided for making a coated abrasive article comprising:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises a polymerizable pressure-sensitive adhesive precursor;
(2) fully curing the make coat precursor to a pressure-sensitive adhesive;
(3) applying a plurality of abrasive grains into the cured make coat;
(4) applying a size coat precursor; and (5) fully curing the size coat precursor.
A preferred embodiment of the second method for making a coated abrasive article comprises:
(1) applying a make coat precursor to a hacking, wherein the make coat precursor comprises:
(a) at least one ethylenically unsaturated monomer, and (b) at least one of a cationically polymerizable monomer or a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
(i) at least one cationically polymerizable monomer or polyurethane precursor initiator, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt, provided that component (b) is a cationically polymerizable monomer, and (iii) optionally, at least one free radical initiator;
(2) exposing the make coat precursor to an energy source to activate either sequentially or simultaneously, the canonically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer; or both;
(3) fully curing the make coat precursor;

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(4) applying a plurality of abrasive grains into the make coat precursor;
(5) applying a size coat precursor; and (6) fully curing the size coat precursor.
Advantageously, when practicing the second method, the make coat precursor, when fully cured is a tacky, adhesive layer, such as a pressure sensitive adhesive. Advantageously, the polymerized make coat does not flow and wet-up Lhe sides of the abrasive grains and permits a "smooth," evenly-coated, substantially mono-layer of abrasive grains. When the ethylenically unsaturated monomer is initiated by the application of eLrctron beam irradiation, a free radical initiator is not required. In other instances, the ethylenically unsaturated monomer is initiated by adding a catalytically-effective amount of at least one free radical initiator.
Advantageously, the ethylenically unsaturated monomer polymerization can be initiated by a free radical source, such as by electron beam radiation or with a catalytically-effective amount of a curing agent or initiator. If a curing agent or initiator is employed, the free radical source can be generated by exposing the curing agent or initiator to either heat or a radiation energy source.
Examples of typical radiation energy sources include electron beam, ultraviolet light and visible light.
During the manufacture of the abrasive article, the make coat precursor and the size coat precursor are applied typically in a liquid or semi-liquid state since the resin is in an uncured or unpolymerized state. The size coat precursor can be any glutinous or resinous adhesive. Examples of such resinous adhesives include:
phenolic resins, acrylate resins, aminoplast resins, epoxy monomers, urethane resins, polyester resins, urea-formaldehyde resins and combinations thereof.
In general, for a fully cured make coat or size coat, 90% or more of the potential reactive groups on the monomer or precursor have been reacted. The resin in both the make coat precursor and the size coat precursor is fully cured or polymerized to form the make coat and the size coat of the coated abrasive.
Additionally, the make coat precursor and/or the size coat precursor can contain additives that are commonly used in the abrasive~industry. These additives _ ~ A.
., _7_ include fillers, grinding aids, colorants, coupling agents, surfactants, lubricants, plasticizers, and mixtures thereof.
The advantages of the invention are the reduced tendency to form multiple layers of abrasive grains and the improved performance associated with the coated abrasive of this invention.
Advantageously, polymerization, at Ieast partially of the make coat precursor, is initiated prior to application of abrasive grains and minimizes the amount of abrasive grain coated onto the backing. While not being bound by theory, it is believed that this phenomena is achieved by one of two means.
The first pertains to the surface roughness of the coated abrasive backing. Most coated abrasive backings are inherently rough, that is, having a plurality of peaks and valleys. This roughness results in an increased surface area. This in turn allows more abrasive grain to be coated than would be the case with a totally smooth substrate while simultaneously reducing the number of abrasive grains that are in a functional location.
A second problem occurring associated with the backing roughness is that the make coat precursor is usually applied in such a way that more material is deposited in the valleys than on the peaks. If enough of the make coat precursor is applied to the peaks to firmly anchor a monolayer of abrasive grain, the excess make coat precursor in the valleys results in multiple layers of abrasive grains at these locations. If the polymerization of the make coat precursor is initiated before the abrasive grains are applied, then sufficient make coat precursor can be used to fill up the valleys, thereby decreasing the surface area. This in turn leads to a reduction in the abrasive grain coating weight. Since the make coat precursor is no longer liquid at this point, the increased amount of make coat precursor present in the valleys of the backing does not result in the multiple layers of abrasive grain at these locations as would otherwise be the case.
In this application:
"catalytically-effective amount"~ means a quantity sufficient to effect polymerization of the curable composition to a polymerized product at least to a degree to cause an increase in the viscosity of the composition;
"cationically polymerizable monomer" means materials that undergo _g_ cationic polymerization and include 1,2-, 1,3-, and 1,4-cyclic ethers, vinyl ethers, cyclic formats, and cyclic organosiloxanes.
"cured" and "polymerized" can be used interchangeably "epoxy monomer" means monomeric materials, oligomeric materials or polymeric materials which contain an oxirane ring, such that the epoxy monomer is polymerizable by ring opening;
"ethylenically unsaturated monomer" means those monomers that polymerize by a free-radical mechanism;
"fully cured" means the make coat precursor or size coat precursor has been polymerized or substantially converted;
"make coat precursor" means the polymerizable composition applied over the front surface of a backing that secures abrasive grains to the backing;
"organometallic compound" means a chemical substance in which at least one carbon atom of an organic group is bonded to a metal or nonmetal atom (Hawle~'s Condensed Chemical Dictionary 858 (N. Sax & R. Lewis 11th ed.
1987);
"polyisocyanate" means an aliphatic or aromatic isocyanate compound containing 2 or more isocyanate groups; and "polyurethane precursor" means a mixture of one or more monomers of the type including polyisocyanates, and one or more monomers of the type including polyols. Compounds bearing at least two isocyanate-reactive hydrogen atoms may be substituted for diols and polyols; the ratio of isocyanate groups to isocyanate-reactive hydrogen atoms is 1:2 to 2:1;
"polyol" means an aliphatic or aromatic compound containing 2 or more hydroxyl groups;
"pressure sensitive adhesive precursor" means a palymerizable material that when fully cured has the properties of (1) being tacky, (2) exerting a strong holding force, (3) having sufficient cohesiveness and elasticity that it can be removed from smooth surfaces without leaving a visible residue, and (4) requiring no activation by water, solvent or heat to become tacky; and "size coat ;precursor" means the polymerizable composition applied over the abrasive grainslmake coat precursor and further reinforces the abrasive grains.

~~~9 z'?G~~s BRIEF DESCRIPTION OF THE DRA~JVING
Figure 1 illustrates in enlarged cross section a segment of a coated abrasive containing a backing.
$ DETAILED DESCRIPTION OF THE .PREFERRED EMBODIMENTS) This invention pertains in particular to the coated abrasive article and to a method of making a coated abrasive article.
Refernng to Figure 1, in a preferred embodiment coated abrasive article 30 is typically cloth- or paper-backed. Overlaying backing 36 is make coat 38 in 30 which is embedded a plurality of abrasive grains 40. Size coat 42 is coated over make coat 38 and the plurality of abrasive grains 40.
In a preferred embodiment of the present invention, a coated abrasive article is provided comprising (1) a backing, (2) a make coat layer, wherein the make coat layer comprises (a) an ethylenically unsaturated monomer, (b) a 15 cationically polymerizable monomer or a polyurethane precursor, and (c) a curing agent comprising (i) at least one organometallic complex salt, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt, and (iii) optionally, at least one free radical initiator, 20 (3) plurality of abrasive grains and (4) a size coat layer.
In another aspect of the present invention, a first method is provided for making a coated abrasive article comprising:
(I) applying a make coat precursor to a backing, wherein the make coat precursor comprises:
25 (a) at least one ethylenically unsaturated monomer, and (b) at least one of a cationically polymerizable monomer or a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
(i) at least one cationically polymerizable monomer or 30 polyurethane precursor initiator, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation r,! f-A
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complex with the metal ion of the organometallic complex salt, provided component (b) is a canonically polymerizable monomer, and (iii) optionally, at least one free radical initiator;
(2) exposing the make coat precursor to an energy source to activate the organometallic complex salt;
(3) partially polymerizing, either sequentially or simultaneously, the cationically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer; or both;
(4) applying a plurality of abrasive grains into the make coat precursor;
(~) applying a size coat precursor;
(6) fully curing the make coat precursor; and (7) fully curing the size coat precursor.
When using the first method, it is preferable that steps 1 through 4 are accomplished in the order as written. Partial polymerization of (a) the cationically polymerizable monomer or the polyurethane precursor, or (b) the ethylenically unsaturated monomer, or both (a) and (b), results in a tacky, pressure-sensitive adhesive-like layer. Advantageously, the partially polymerized make coat does not flow and wet-up the sides of the abrasive grains and permits a "smooth,"
evenly-coated, substantially mono-layer of abrasive grains. It is an another advantage of the present invention that steps 5 and 6 may be accomplished in any order, and that the order of steps 5 and 6 as written is merely one of a number of routes that may be utilized in practicing the present invention. When the ethylenically unsaturated monomer is initiated by the application of electron beam irradiation, a free radical initiator is not required. In other instances, the ethylenically unsaturated monomer is initiated by adding a catalytically-effective amount of at least one free radical initiator.
In yet another aspect of the present invention, a second method is provided for making a coated abrasive article comprising:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises a polymerizable pressure-sensitive adhesive precursor;
(2) fully curing the make coat precursor to a pressure-sensitive adhesive;

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(3) applying a plurality of abrasive grains into the cured make coat;
(4) applying a size coat precursor; and (5) fully curing the size coat precursor.
A preferred embodiment of the second method for making a coated abrasive article comprises:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises:
(a) at least one ethylenically unsaturated monomer, and (b) at least one of a canonically polymerizable monomer or a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
(i) at least one canonically polymerizable monomer or polyurethane precursor initiator, (ii) optionally, at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt, provided component (b) is a cationically polymerizable monomer, and (iii) optionally, at least one free radical initiator;
(2) exposing the make coat precursor to an energy source to activate either sequentially or simultaneously, the canonically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer; or both;
(3) fully curing the make coat precursor;
(4) applying a plurality of abrasive grains into the make coat precursor;
(5) applying a size coat precursor; and (6) fully curing the size coat precursor.
Advantageously, when using the second method, the make coat precursor, when fully cured is a tacky, adhesive layer, such as a pressure sensitive adhesive.
Advantageously, the polymerized make coat does not flow and wet-up the sides of the abrasive grains and permits a "smooth," evenly-coated, substantially mono-layer of abrasive grains. Preferably, the ethylenically unsaturated monomer is initiated by the application of electron beam irradiation and as such a free radical initiator is not required, although such an initiator may be present. In other instances, the f;thylenically unsaturated monomer is initiated by adding a catalytically-effective amount of at least one Free radical indator.
The backing used in the preferred embodiment may be any substrate type .
material, generally known to those skilled in the art and may include, but is not limited to nonwoven substrates, polymeric film, paper, cloth, vulcanized fibre, metal plates and treated versions and combinations thereof.
The make coat precursor is applied to the front side by any conventional coating technique known to those skilled in 'the art and may include, but is not limited to roll coating, die coating, spray coating and curtain coating. The preferred coating technique is knife coating.
The make coat precursor comprises (a) an ethylenically unsaturated monomer, (b) a cationically polymerizable monomer or a polyurethane precursor and (c) a catalytically-effective amount of a curing agent (or initiator) for either the cationically polymerizable monomer or the polyurethane precursor, (d) optionally, at least one thermally decomposable ester reaction product of a teritary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt, provided component (b) is an epoxy monomer and (e) optionally, at least one free radical initiator.
Ethylenically unsaturated monomers that undergo free radical polymerization include (meth)acrylates, (meth)acrylamides and vinyl compounds.
, The ethylenically unsaturated monomers can be a mono-, multi-functional, or a .
mixture thereof.
Examplta of such ethylenically unsaturated monomers include mono-, di-, or polyacrylate and methacrylates, methyl acrylate, methyl methacryiate, ethyl acrylate, isopropyl methacrylate, isooctyl acrylate, acrylic acid, n-hexyl aerylate, stearyl acrylate, allyl acrylate, vinylazlactones as described in U.S. Patent 4,304,705, isobornyl acrylate, isobornyl methacrylate, acrylic acid, N-vinyl caprolactam, acrylonitrile, allyl acrylate, l;lycerol diacrylate, glycerol triacrylate, ethylene glycol diacrylate, diethylene glycol diacrylate, 1,6-hexanediol diacrylate, 2-phenoxyethylacrylate, 1,4-cyclohexanediol diacrylate, 2,2-bis[1-(3-acryloxy-2-hydroxy)]propoxyphenylpropane, tris(hydroxyethyl)isocyanurate trimethacrylate;

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the bis-acrylates and bismethacrylates of polyethylene glycols of molecular weight of 200 to 500, ethylene glycol diacrylate, butyl acrylate, tetrahydrofurfuryl acrylate, N-vinyl pyrrolidone, diethyleneglycol diacrylate, triethyleneglycol diacrylate, tetraethyleneglycol diacrylate, 1,4-butanediol diacrylate, triethyleneglycol dimethacrylate, 1,3-propanediol diacrylate, 1,3 propanediol dimethacrylate, trimethylolpropane triacrylate, 1,2,5,-butanetriol trimethacrylate, 4,5-cyclohexanediol diacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, pentaerythritol tetramethacrylate, sorbitol hexacrylate, bis[1-(2-acryloxy)]-p-ethoxyphenyldimethylmethane, bis[l-(3-acryloxy-2-hydroxy)]-p-propoxyphenyl-dimethylmethane, copolymerizable mixtures of acrylated monomers such as those of U.S. Patent No. 4,652,274 and acrylated oligomers such as those of U.S. Patent No. 4,642,126; bireactive monomers such as epoxy (meth)acrylates, isocyanato (meth)acrylates, and hydroxy (meth)acrylates, hydroxyethyl (meth)acrylate, hydroxypropyl (meth)acrylate, isocyanatoethyl (meth)acrylate, glycidyl (meth)acrylate, and m-isopropenyl-alpha, alpha-dimethylbenzylisocyanate, unsaturated amides, such as acrylamide, N,N-dimethyl acrylamide, methylene bis-acrylamide, methylene bis-methacrylamide, 1,6-hexamethylene bisacrylamide, , diethylene triamine tris-acrylamide and beta-methacrylamidoethyl methacrylate;
and vinyl compounds such as styrene, divinylbenzene, diallyl phthalate, divinyl succinate, divinyl adipate, divinyl phthalate. Mixtures of two or more monomers can be used if desired. Preferred ethylenically unsaturated monomers include 1,4-butanediol diacrylate, N,N-dimethyl acrylamide, triethyleneglycol diacrylate, tetraethyleneglycol diacrylate, trimethylolpropane triacrylate, tetrahydrofurfuryl acrylate, N-vinyl pyrrolidone, isooctyl acrylate, N-vinyl caprolactam, 1,6-hexanediol diacrylate, and butyl acrylate.
The ethylenically unsaturated monomers polymerize or cure by a free radical polymerization mechanism. This polymerization is initiated by a free radical source and can be generated by electron beam radiation or by an appropriate curing agent or initiator. If a curing agent or initiator is employed, then a free radical source can be generated by exposing the curing agent or initiator to either heat or a radiation energy source. Examples of radiation energy sources include electron beam, ultraviolet light or visible light.

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Canonically polymerizable materials that undergo cationic polymerization include 1,2-, 1,3- and 1,4-cyclic ethers (also designated as 1,2-, 1,3- and 1,4-epoxides), vinyl ethers, cyclic formats, and cyclic organosiloxanes.
The term canonically polymerizable monomer is meant to include monomeric materials, oligomeric materials or polymeric materials that contain an oxirane ring, that is C_____C
O
and the compound is polymerized by ring opening. This reaction is not a condensation reaction, but rather an opening of the epoxy ring initiated by an acidic or basic catalyst. Such materials may vary greatly in the nature of their backbones and substituent groups. For example, the backbone may be of any type such that there is an active hydrogen atom which is reactive with an oxirane ring at room temperature. Representative examples of acceptable substituent groups include halogens, ester groups, ether groups, sulfonate ester groups, siloxane groups, nitro groups, and phosphate ester groups. The molecular weight of the epoxy containing materials can vary from about 60 to about 4000, and preferably range from about 100 to about 600. Mixtures of various epoxy-containing materials can be used in the compositions of this invention.
Epoxy-containing materials that are particularly useful in the practice of this invention include glycidyl ether monomers of the formula R°'(OCH2CH-----CH~m O
wherein R" is an alkyl or aryl group and m is an integer of 1 to b, inclusive.
Representative examples of these are the glycidyl ethers of polyhydric phenols obtained by reacting a polyhydric phenol with an excess of a chlorohydrin, such as epichlarohydrin. Specific examples of such materials include 2,2-bis[4-(2,3-epoxypropoxy)-phenyljpropane (diglycidyl ether of bisphenol A) and commercially available materials under the trade designation "Epon 828", °'Epon 1004" and "Epon 1001F" available from Shell Chemical Co., "DER-331 ", "DER-332" and . "DER-334" available from Dow Chemical Co., flame retardant epoxy resins (e.g., "DER-580", a brominated bisphenol type epoxy resin available from Dow Chemical Co.), glycidyl ethers of phenol formaldehyde novolac (e.g., "DEN-431"
and "DEN-428" available from Dow Chemical Co.), and resorcinol diglycidyl ether. Additional examples of epoxides of this type that can be used in the practice of this invention are described in U.S. Patent No. 3,018,262, and in Lee and Neville, Handbook of E',,~xy Resins, Appendix A 1967).
Corrunercially available epoxy-containing materials useful in this invention include ~cycloaliphatic epoxide monomers such as the epoxycyclohexanecarboxylates, typified by 3,4-epoxycyclohexylmethyl 3,4-epoxyc.yclohexanecarboxylate~,4-epoxy-2-methylcyclohexylmethyB,4-epoxy-2-methylcyclohexanecarboxylate, bis(3.4-epoxy-6-methylcyclohexylmethyl) adipate, and 3,4-epoxy-6-methylcyclohexane, vinylcyclohexande dioxide, and bis(2,3-epoxycyclopentyl i eaher, (7ther useful epoxides of this nature are described in U.S. Patent No. 3.1 x'7,()99.
Additionally commercially available epoxy-containing materials that can be used in the practice of this invention include octadecyl oxide, epichlorohydrin, styrene oxide, glycidol, butyl glycidyl ether, glycidyl acrylate and methacrylate, epoxy n-mdiiied polypropylene glycol, peroxidized polybutadiene, silicone resins containing epoxy functionality, and copolymers of acrylic acid esters of gIycidol, such as glycidyl acrylate and glycidyl methacrylate, with one or more copolymeriz~able vinyl compounds, such as methyl methacrylate, vinyl chloride, and styrene. Examples of such copolymers are 1:1 styrene:glycidyl methacrylate, l:l methyl methacrylate:glycidyl acrylate, and 62.5:24:13.5 methyl methacrylate:ethyl acrylate:glycidyl methacrylate.
The :polymeric epoxides include linear polymers having terminal epoxy groups (e.g., a diglycidyl ether of a polyoxyalkylene glycol), polymers having skeletal oxirane units (e.g., polybutadiene polyepoxide), and polymers having pendant epo;Xy groups (e.g., glycidyl methacrylate polymer or copolymer). The epoxides may be individual compounds, but are generally mixtures containing one, two or more epoxy groups per molecule. "The "average" number of epoxy groups .~ ~a ~ ~!7 ~y ~f~ 4Y ~~ ~~I Y9 per molecule is determined by dividing the total number of epoxy groups by the epoxy molecules present.
Other cationically-sensitive monomers that can be used in the present invention include vinyl ethers, such as vinyl methyl ether, vinyl ethyl ether, vinyl n-butyl ether, vinyl 2-chloroethyl ether, vinyl isobutyl ether, vinyl phenyl ether and vinyl 2-ethylhexyl ether, vinyl ethers of substituted aliphatic alcohols such as 1,4-di(ethenoxy)butane, vinyl 4-hydroxy-butyl ether; cyclic formats such as trioxane, 1,3-dioxolane, 2-vinyl-1,3-dioxohne, and 2,-methyl-1,3-dioxolane;
and cyclic siloxanes that can contain various groups attached to the silicop atom such as a hydrocarbon radical (alkyl, aryl, alkaryl), an alkenyl hydrocarbon radical (vinyl, allyl or acryloyloxy-alkyl), a halogenated hydrocarbon radical, a carboxy-containing hydrocarbon radical or ester group, a cyanohydrocarbon radical, hydrogen, halogen or a hydroxy group.
When practicing the first method of the present invention, the preferred cationically polymerizable monomers are diglycidyl ethers of bisphenols. When practicing the second method of the present invention, the preferred cationically polymeriaable monomers are cycloaliphatic epoxy monomers.
The polyisocyanate component of the polyurethane precursors of the invention may be any aliphatic, cycloaliphatic, aromatic or heterocyclic polyisocyanate, or any combination of such polyisocyanates, particularly suitable polyisocyanates correspond to the formula:
Q~C~)p wherein p is an integer between 2 to 4, and Q represents an aliphatic hydrocarbon di-, tri-, or tetra- group containing from 2 to 100 carbon atoms, and zero to heteroatoms, a cycloaliphatic hydrocarbon radical containing 4 to 100 carbon atoms and zero to 50 heteroatoms, an aromatic hydrocarbon radical or heterocyclic aromatic radical containing from 5 to 15 carbon atoms and zero to 10 hetexoatoms, or an aliphatic hydrocarbon radical containing from 8 to 100 .carbon atoms and zero to 50 heteroatoms. The heteroatoms that can be present in Q include non-peroxidic oxygen, sulfur, nonamino nitrogen, halogen, silicon, and non-phosphino phosphorus.

f~~
~'.,,"o ~:1 ~~ ~ ~' ~
' 17-Examples of polyisocyanates are as follows: ethylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 3,4,4-trimethyl hexamethylene diisocyanate, 1,12-dodecane diisocyanate, cyclobutane-1,3-diisocyanate, cyclohexane-1,3- and -1,4-diisocyanate and mixtures of these isomers,1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane(seeGerman Auslegenschrift No. 1,202,785, U.S. Patent Ielo. 3,401,190), 2,4- and 2,6-hexahydrotolylene diisocyanate and mixtures of these isomers, hexahydro-1,3-and/or -1,4-phenylene diisocyanate, perhydro-2,4'- andlor -4,4' diphenylmethane diisocyanate, 1,3- and 1,4-phenylene diisocyanate, 2,4- and 2,6-tolylene diisocyanate and mixtures of these isomers, diphenylmethane-2,4'- and-/or -4,4'-diisocyanate, naphthylene-1,5-diisocyanate, and the reaction products of four equivalents of the aforementioned isocyanate containing compound with a compound containing two isocyanate-reactive groups.
It is also within the scope of the present invention to use, for example, triphenylmethane-4,4',4"-triisocyanate,polyphenylpolymethylenepolyisocyanates, m- and p-isocyanatophenylsulfonyl isocyanates, perchlorinated aryl polyisocyanates, polyisocyanates containing carbodiimide groups, norbornane diisocyanates, polyisocyanates containing allophanate groups, polyisocyanates containing isocyanurate groups, polyisocyanates containing urethane groups, polyisocyanates containing acrylated urea groups, polyisocyanates containing biuret groups, polyisocyanates prepared by telomerization reactions of the type described in U.S. Patent 3,654,106, polyisocyanates containing ester groups, polyisocyanates containing polymeric fatty acid groups, and reactions products of any of the above mentioned diisocyanates with acetals; or mixtures of any of the above polyisocyanates.
Also useful are blocked polyisocyanates, many of which are commercially available, wherein the blocking group can be, for example, phenol, epsilon-caprolactam, hydroxamic acid ester, ketoxime, t-butyl acetoacetate and others as described in Wicks, Z.W., Jr. Progress in Organic Coatines, 9, 3-28 (1981}.
Preferred polyisocyantes are aliphatic, such as hexamethylene diisocyante, the isocyanurate and the biuret thereof, such as those commerically available under the trade designation °'DESMODUR I~T" (available from Mobay Corp.), 4,4'-f.~ -~ ~a ~~~~
s~,~~~SY)~W:~
_18_ methylenebis(cyclohexyl isocyanate); 1-isocyanato-3,3,5-trirnethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate) and the biurets thereof;
the tolylene diisocyanates and the isocyanurates thereof; the mixed isocyanurate of tolylene diisocyanate and hexamethylene diisocyanate; the reaction product of one mole of trimethylol propane and three moles of tolylene diisoscyanate and crude diphenylmethane diisocyanate.
Suitable isocyanate-reactive groups contain at least two isocyanate-reactive hydrogen atoms. They can be high or low molecular weight compounds having a weight average molecular weight of from about SO to 50,000. Useful compounds are those including amino groups, thiol groups, carboxyl groups, and hydroxyl groups, Preferably, isocyanate-reactive compounds containing hydroxyl groups, particularly compounds containing from about 2 to 50 hydroxyl groups, and more particularly, compounds having a weight of from about 200 to 25,000 more preferably from about 200 to 20,000, for example, polyesters, polyethers, polythioethers, polyacetals, polycarbonates, poly(meth)acrylates, and polyester amides, containing at least 2, generally from about 2 to 8, but preferably from about 2 to 4 hydroxyl groups, or even hydroxyl-containing prepolymers of these compounds. It is, of course, possible to use mixtures of the above-mentioned compounds containing at least two hydroxyl groups and having a molecular weight of from about 50 to 50,000 for example, mixtures of polyethers and polyesters.
Low molecular weight compounds containing at least two isocyanate-reactive hydrogen atoms (molecular weight from about 50 to 400) suitable far use in accordance with the present invention are compounds preferably containing hydroxyl groups and generally containing from about 2 to 8, preferably from about 2 to 4 isocyanate reactive hydrogen atoms. It is also possible to use mixtures of different compounds containing at least two isocyanate-reactive hydrogen atoms and having a molecular weight in the range of from about SO to 400. Examples of such compounds are ethylene glycol, 1,2- and 1,3-propylene glycol, 1,4- and 2,3-butylene glycol, 1,5-pentane diol, 1,6-hexane diol, 1,8-octane diol, neopentyl glycol, 1,4-bis-hydroxymethyl cyclohexane,. 2-methyl-1,3-propane diol, dibromobutene diol, glycerol, trimethylolpropane, 1,2,6-hexanetriol, _ ,~ r.~~

trimethylolethane, pentaerythritol, quinitol, mannitol, sorbitol, diethylene glycol, triethylene glycol, teraethylene glycol, higher polyethylene glycols, dipropylene glycol, higher polypropylene glycols, dibutylene glycol, higher polybutylene glycols, 4,4'-dihydroxy diphenyl propane and dihydroxy methyl hydroquinone.
S Other polyols suitable for the purposes of the present invention are the mixtures of hydroxy aldehydes and hydroxy ketones or the polyhydric alcohols obtained therefrom by reduction, which are formed in the autocondensation of formaldehyde, polymers thereof and hydrates thereof, in the presence of metal compounds as catalysts and compounds capable of enediol formation as co catalysts.
Other isocyanate reactive compounds are polyols having molecular weights in the range of 200 to 20,000 grams per mole, and containing two or more primary hydroxyl groups per molecule.
Preferred polyols can be of hydroxylalkylated bisphenol derivatives.
Preferred diols in this group can be represented by the formula:
CH_O_R1_Al2_C_R2 wherein R1 is either a straight, branched, or cyclic alkylene (such as methylene, ethylene, and decylene) group having of I to 10 carbon atoms or an aralkylene group having of 7 to 14 carbon atoms such as benzylidene. R2 and R3 independently may be an alkyl groups, aralkyl group, cycloalkyl groups, alkaryl group, or an aryl group of 1 to 30 carbon atoms, preferably methyl, ethyl and trifluoromethyl, and zero or 1 to 10 heteroatoms, and R2 and R3 taken together can comprise alkylene groups, cycloalkylene groups, arylene group, alkarylene group, or aralkylene group containing 2 to 660 carbon atoms, and none or 1 to heteroatoms. "A" can be a substituted or unsubstituted arylene groups, preferably having 6 to 12 carbon atoms, most preferably p-phenylene, o-phenylene, and dimethylnaphthalene.
Specific preferred hydroxyalkylated bisphenols are 2,2-bis-4-(2 hydroxyethoxyphenyl)butane, hydroxyethylated bisphenol of butanone, 2,2-bis-4 (2-hydroxyethoxyphenyl)hexafluoropropane and 1,2-bis-4-(2 hydroxyethoxyphenyl)propane,2,2-bis-4-(2-hydroxyethoxyphenyl)norbornane~,2 c li~~'n~s -20- ~~'..1t7,~'3~.~a bis-4-(2-hydroxyethoxyphenyl)-5,6-cyclopentanorbornane and 1,1-bis-4-(2 hydroxyethoxyphenyl)cyclohexane. Polyurethanes prepared from the polyurethane precursors and useful in the present invention preferably have a glass transition temperature of greater than room temperature and more preferably greater than 70°C.
Another group of monomers which are useful in compositions of the invention are bireactive monomers that serve as crosslinkers, that is, those that possess at least one free-radically polymerizable group and one isocyanate or isocyanate reactive functionality. Such monomers include, for example, 2-isocyanatoethyl methacrylate, 3-isopropenylphenyl isoeyanate, hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl methacrylate and hydroxybutyl acrylate. Bireactive monomers can comprise up to 25 mole percent of the isocyanate or isocyanate-reactive groups, preferably they can comprise less than 5 mole percent of the isocyanate reactive groups and up to 50 mole percent of free-radically polymerizable monomers, preferably less than 25 mole percent of free-radically polymerizable monomers. Most preferably, the compositions are free of bireactive monomers.
Weight ratios of the make coat precursor typically range from about S to 95 parts by weight, preferably 40 to 85 parts by weight of ethylenically unsaturated monomer, and 5 to 95 parts by weight, preferably 15 to 60 parts by weight of either the cationically polymerizable monomer or the polyurethane precursor. Additionally, the curing agent for the ethylenically unsaturated monomer, and the cationically polymerizable monomer or the polyurethane precursor is typically less than 20 parts by weight, preferably less than 8 parts by weight, more preferably less than 4 parts by weight.
The abrasive grains of the invention have a Moh hardness of at least 7, preferably at least 8. Typical examples of abrasive grains include aluminum oxide, heat treated aluminum oxide, ceramic aluminum oxide, silicon carbide, diamond, ~alumina zirconia, cerium oxide, boron carbide, cubic boron nitride, garnet and mixtures thereof. The abrasive grains can be applied by drop coating . or preferably by e:fectrostatic coating.

A si::e coat precursor applied over the abrasive grains and the make coat precursor m.ay be any resinous or glutinous adhesive. Examples of such size coat precursors include phenolic resins, urea-formaldehyde resins, melamine resins, acrylate resins, urethane resins, epoxy monomers, polyester resins, aminoplast resins and combinations and mixtures thereof. The size coat precursor can comprise a cationically polymerizable monomer, an ethylenically unsaturated monomer, a mixture of each, or a mixture of canonically polymerizable monomers ethylenically unsaturated monomers. The preferred size coat precursor is a phenolic resin or an epoxy monomer. The size coat can be applied by any conventional techniques lc:nown to those skilled in the art and include but are not limited to ro~l coating. die coating, curtain coating and preferably spray coating.
The make coat prt.c.ursor andior the size coat precursor of the invention can additionally contain optional additives that are well known in the coated abrasive art. These additives include fillers, fibers, lubricants, grinding aids, wetting agents, surfactants, colorants, coupling agents, plasticizers, and suspending agents.
Preferred fillers include calcium carbonate, calcium oxide, calcium metasilicate, alumina trihydrate, cryol~te, magnesia, kaolin, quartz, and glass. Fillers that function as grinding aids are crvolite. potassium fluoroborate, feldspar, and sulfur.
The fillers can he used ir. amounts up to about 250 parts, preferably from about 30 to about :150 parts, peer l0U pans of the make or size coat precursor while retaining good flexibility and toughness of the cured binder. The amounts of these materials are selected to give the properties desired.
The preferred curing agent for both the canonically polymerizable monomer and the polyurethane precursor are salts of organometallic complex rations, such as described in European Patent Application 109,581 (cationically polymerizable monomers) and U.S. Patent Nos. 4,740,577 (polyurethane precursors) and 5,059,701 (canonically polymerizable monomers and polyurethane precursors).
Another example of a curing agent is a mixture of a salt of organometallic complex ration and an oniur~n salt as described in U.S. Patent Na. 4985,340.
Suitable salts of organometallic complex rations include but are not limited to, those salts having the f-allowing formula:

_22-~~-1)(L2)M~+q ~'n wherein Mp represents a metal selected from the group consisting of Cr, Mo, W, Mn Re, Fe, and Co;
Ll represents 1 or 2 ligands contributing pi-electrons that can be the same or different ligand selected from 'the group of: substituted and unsubstituted eta3-allyl, eta5-cyclopentadienyl, and eta~-cycloheptatrienyl, and eta6-aromatic compounds selected from eta6-benzene and substituted eta6-benzene compounds and compounds having 2 to 4 fused rings, each capable of contributing 3 to 8 pi-electrons to the valence shell of Mp;
LZ represents none, or 1 to 3 ligands contributing an even number of sigma-electrons Lhat can be the same or different ligand selected from the group of: carbon monoxide, nitrosonium, triphenyl phosphine, triphenyl stibine and derivatives of phosphorus, arsenic and antimony, with the proviso that the total electronic charge contributed to Ml' results in a net residual positive charge of q to the complex;
q is an integer having a value of 1 or 2, the residual charge of the complex canon;
Y is a halogen-containing complex anion selected from BF4 , AsF6 , PF6 , SbFSOH-, SbFb , and CF3S0~ ; and n is an integer having a value of 1 or 2, the number of complex anions required to neutralize the charge q on the complex ration;
Examples of suitable salts of organometallic complex rations useful in the composition of the invention include the following:
(eta6-benzene)(eta$-cyclopentadienyl)iron(1 +~exafluoroantimonate (eta6-toluene)(etas-cyclopentadienyl)iron(1+) hexafluoroarsenate (eta~-cumene)(eta5-cyclopentadienyl)iron(1+) hexafluorophosphate (eta6-p-xylene)(etas-cyclopentadienyl)iron(1 +) hexafluoroantimonate -23 _ ~~~~~~3~
(eta6-xylenes(mixed isomers))(etas-cyclopentadienyl) iron (1+) hexafluoroantinomate (eta6-xylenes(mixed isomers))(eta$-cyclopentadienyl) iron {1+) hexafluorophosphate (eta6-o-xylene)(etas-cyclopentadienyl)iron(1+) triflate (eta6-m-xylene)(eta5-cyclopentadienyl)iron(1+) tetrafluoroborate (eta6-mesitylene)(etas-cyclopentadienyl)iron(1 +) hexafluoroantimonate (eta6-hexamethylbenzene){etas-cyclopentadienyl)iron( 1 +) pentafluarohydroxyantimonate (eta6-naphthalene)(eta$-cyclopentadienyl)iron(1 +)tetrafluoroborate (eta6-pyrene)(eta5-cyclopentadienyl)iron(1+) triflate (eta6-perylene)(etas-cyclopentadienyl)iron(1+) hexafluoroantimonate (eta6-chrysene)(etas-cyclopentadienyl)iron(1 +) pentafl uorohydroxyantimanate {eta~-acetophenane)(etas-methylcyclopentadienyl)iron(1 +) hexafluoroantimonate (eta6-fluorene)(eta~-cyclapentadienyl)iron{1+) hexafluoroantimonate Examples of preferred salts of organometallic complex cations useful in the composition of the invention include one or more of the following:
(eta6-xylenes(mixed isomers))(eta~-cyclopentadienyl) iron (1+) hexafluoroantinomate (eta6-xylenes(mixed isomers))(etas-cyclopentadienyl) iron (1+) hexafluorophosphate (eta6-m-xylene)(eta~-cyciopentadienyl)iron(1+) tetrafluoroborate (eta6-o-xylene)(eta$-cyclopentadienyl)iron(1 +) hexafluoroantimonate (et<16-p-xylenes)(etas-cyclopentadienyl)iron(1+) triflate (eta6-mesitylene)(etas-cyclopentadienyl)iron(1 +) hexafluoroantimonate {et<1~-cumene)(eta5-cyclopentadienyl)iron(1 +) hexafluorophasphate _ 24 ._ (eta6-mesitylene)(etas-cyclopentadienyl)iron(1 +) pentafluorohydroxyantimonate (eta6-toluene;H(etas-cyclopentadienyl)iron(1 +) hexafluoroarsenate The curing agent for cationically polymerizable monomers may include a salt having ar.~ onium ration and a halogen-containing complex anion of a metal or metalloid as described in U.S. Patent 4~~5I,138.
While it is not preferred, it would be within the scope of the present invention to pure the canonically polymerizable monomers or the polyurethane precursor using suitable curing agents, such as those that are thermally-activated.
Epoxy curin8 agents include. but are not limited to aliphatic and aromatic primary amines; Lxwis acids, such as aluminum triehloride, aluminum tribromide, boron trifluoride, antimony pentt~fluoride, titanium trifluoride. Further, boron trifluoride complexes, .~uch as BF ~~monoethanolamine; imidazoles, such as 2-ethyl-4-methylimidazole; hydrazides, such as aminodihydrazide; guanidines, such as tetramethyl guanidine: dicv~trtdiamide: and polybasic acids and their anhydrides.
Such polyurethane precursor curint agents include, but are not limited to conventional natall-'sts. including tertia.rv amines, and tin and bismuth salts.
Examples of curing agents or initiators, that generate a free radical source when expos~rd to ultraviolet light radiation energy include quinones, benzophenonea, nitroso connpounds, acryl halides, hydrazones, benzoin ethers, benzil ketals, thioxanthones, and acetophenone derivatives. Additional references to free radical photoinitiator systems for ethylenically unsaturated compounds are included in LI.S. Patent :No. 3,887,450 and U.S. Patent No. 3,895,949. For ultraviolet light curing, in order to fully polymerize the ethylenically unsaturated monomer, the make coat ,Eyrecursor should be exposed to an energy level at least between 100 to 700 mmlliJoules~cm-2, preferably between 400 to 600 milliJoules~crrt-2.
Optionally, it is within the scope of this invention to include photosensitizers or photoaccelerators in the polymerizable compositions. Use of photosensitizers or photoat:ceIerators alters the wavelength sensitivity of radiation sensitive corrtlositions. This is particularly advantageous when the photoinitiator -25- ~~~i~~3 i~l~~
employed does not strongly absorb the incident radiation. Use of a photosensitizes or photoaccelerator increases the radiation sensitivity, allowing shorter exposure times and/or the use of less powerful sources of radiation. Any photosensitizes or photoaccelerator may be useful.if its triplet energy is at least 45 kilocalories per mole. Examples of such photosensitizers include pyrene, fluoranthrene, xanthone, thioxanthone, benzophenone, acetophenone, benzil, benzoin and ethers of benzoin, chrysene, p-terphenyl, acenaphthene, naphthalene, phenanthrene, biphenyl, substituted derivatives of the preceding compounds, and the like. When present, the amount of photosensitizes or photoaccelerator used in the practice of this invention is generally in the range of 0.01 to 10 parts by weight, and preferably 0.1 to 10 parts by weight of photosensitizes or photoaccelerator per part of curing system.
When the make coat or size coat precursor contains at least one epoxy monomer, it is also within the scope of the present invention, provided there is no polyurethane precursor present in the make or size coat precursor, to add a catalytically effective amount of a thermally decomposable ester reaction product of a tertiary alcohol and an acid. In general, the thermally decomposable ester reaction products of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt useful in the invention are soluble compounds that upon heating, preferably to a temperature in the range of 60° to 125°C, decompose to release the chelating acid. While not intending to be bound by theory, it is believed that the released acid forms a nonionizing chelation complex with the metal atom, the chelation reaction tends to remove metal atoms from a solution of the photolysed cationic organometallic salt. Thereupon, the acid of the salt anion is released for reaction to catalyze polymerization of the polymerizable material in the system.
The ester reaction products are prepared from tertiary alkyl alcohols and any tertiary alkyl alcohol that forms an ester reaction product with an appropriate acid may be used. Examples of suitable tertiary alkyl alcohols are t-butanol, 1,1-dimethylpropanol,l-methyl-2-ethylpropanol,l,l-dimethyl-n-butanol,l,l-dimethyl-n-octanol, 1,1-diphenylethanol, 1,1-dibenzyl ethanol, 1,1-dimethyl-n-pentanol, 1,1-dimethylisobutanol, 1,1,2,2-tetramethylpropanol, 1-methylcyclopentanol, t-, ~ ~.t ;.;a L: asr4~
~~na t~ v r, 1-methylcyclohexanol, and 1,1-dimethyl-n-hexanol.
Preferred chelating acids for inclusion in acid generating esters of the invention are oxalic, phosphoric and phosphorous acids. Other illustrative chelating acids that are useful include polycarboxylic acids, for example, malonic, succinic, fumaric, malefic, citraconic, aconitic, o-phthalic, trimesic acids and other golycarboxylic acids having less than 3 carbon atoms separating carboxylic groups;
hydroxycarboxylic acids, for example, glycolic, lactic, beta-hydroxybutyric, gamma-hydroxybutyric, tartronic, malic, oxalacetic, tartaric, and citric acids;
aldehydic and ketonic acids, for example, glyoxylic, pyruvic, and ~acetoacetic acids; other acids of phosphorus, chromic acid and vanadic acid.
The acid-generating esters may be prepared by procedures well known in the art. For example, acid-generating esters that incorporate the organic acids may be prepared by procedures described by Karabatsos et al. J. Orb. Chem. 30, 689 (1965). Esters that incorporate phosphate, phosphonate and phosphite esters can be prepared by procedures described by Cox, Jr. J. Am. Chem~Soc'v 80, 5441 (1958); Goldwhite J. Am. Chem. Soc'v 99, 2409 (1957); and Cox, Jr. J. Ora.
Chem. 59, 2600 (1969), respectively.
The acid-generating ester should be relatively nonhydrolyzable and be essentially free of acid. To remove traces of acid from the acid-generating ester, it may be passed through a column filled with an ion exchange resin.
Also useful in accelarating the cationic polymerization when used in combination with a salt of an organometaIlic complex cation and the acid generating ester are peroxides: acylperoxides, such as benzoyl peroxides;
alkyl peroxides, such as t-butylperoxide; hydroperoxides, such as qumyl hydroperoxide;
peresters, such as t-butyl perbenzoate; di-alkyl peroxydicarbonates, such as di-(sec-butyl)peroxydicarbonate; diperoxy ketals; and ketone peroxides, such as methyethylketone peroxide.
A free radical curing agent is not required for electron beam curing of an ethylenicaily unsaturated monomer, although one may be added. For electron beam curing, in order to fully polymerise the ethylenically unsaturated monomer, the make coat precursor should be exposed to a dosage level of 1 to 10 Mrad at an accelerating potential of between 150 to 300 KeV.

'~~~~ j~'~~~a The make and size coat precursors are exposed to an energy source to initiate the polymerization of either the cationically polymerizable monomer or the polyurethane precursor. This exposure may cause the cationicaIly polyrnerizable monomer or the polyurethane precursor to become only partially cured, that is, the polymerization has been started but not yet completed. Alternatively, the exposure to the energy source may cause the cationically polymeriaable monomer or the polyurethane precursor to become fully cured. If the polymerization has been started, it may be fully completed by allowing the make and size coat precursors to stand at room temperature (that is, no additional energy is introduced into the make coat precursor) for a period of time. This time may range from several hours to several days. This time delay is not preferred due to the associated economics.
This energy source can be thermal, which includes both infrared and heat, or radiation energy, which includes electron beam, ultraviolet light and visible light. The time and the amount of energy required to initiate the polymerization or to fully polymerize depends upon the actual materials forming the make coat precursor, type of curing agent, the density and thickness of the make coat precursor.
For thermal curing such as heat, in order to initiate the polymerization of either the canonically polymerizable monomer or the polyurethane precursor, the make coat precursor should be heated for about 1 to 150 minutes at between 30°
to 125°C, preferably 50° to 100°C. For full polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat precursor should be heated for about 5 to 200 minutes at between 50° to 125°C, preferably 75° to 100°C.
Electron beam radiation is also known as ionizing radiation and consists of accelerated particles. For electron beam curing, in order to initiate the polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat precursor or radiation-curable size coat precursor should be exposed to a dosage level of 0.1 to 5 Mrad at an accelerating potential of between 100 to 300 KeV. For full polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat ~q ~:' ~ e~ ~; (~,i G.

precursor or radiation-curable size coat precursor should be exposed to a dosage level of 1 to 10 Mrad at an accelerating potential of between 150 to 300 KeV.
Ultraviolet light radiation means non-particulate radiation having a wavelength within the range of 200 to 400 nanometers, more preferably between 350 to 400 nanometers. For ultraviolet light curing, in order to initiate the polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat precursor is exposed to an enexgy level of at least between 100 to 700 milliJoules~cm 2, preferably between 400 to 600 milliJoules~cm 2. For full polymerization of either the cationically polymerizable monomer or the polyurethane precursor, this energy level may be the same or higher.
Visible light radiation means non-particulate radiation having a wavelength within the range of 400 to 800 nanometers, more preferably between 400 to 550 nanometers. For visible light curing, in order to initiate the polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat precursor is exposed to an energy level of at least between 100 to milliJoules~cm 2, preferably between 400 to 600 milliJoules~cW 2. For full polymerization of either the cationically polymerizable monomer or the polyurethane precursor, the make coat precursor should be exposed to visible light for 5 to 60 seconds, preferably 10 to 30 seconds.
Visible light is the preferred energy source to initiate the polymerization of either the cationically polymerizable monomer or the polyurethane precursor.
The polymerization of the ethylenically unsaturated monomer is typically achieved by the exposure to an ultraviolet light energy source. Thus, when the make coat precursor is exposed to the visible light energy source, the polymerization of the cationically polymerizable monomer or the polyurethane precursor is initiated, but not the polymerization of the ethylenically unsaturated monomer.
For thermal curing, the make coat precursor should be heated for about 1 to 150 minutes at between 30° to 125°C, preferably between about 50° to 100°C.
For electron beam curing, in order to initiate the polymerization of the ethylenically unsaturated monomer, the make coat precursor should be exposed to a dosage level of 0.1 to 5 Mrad at an accelerating potential of between 1 to ~, ~f~ ~1 ~
1 A rs l~ ~c:~ ~3 tJ i-.1 s, s KeV. For ultraviolet light curing, in order to initiate the polymerization of the ethylenically unsaturated monomer, the make coat precursor should be exposed to an energy level of at least between 100 to 700 milliJoules~cni 2, preferably between 400 to 600 milliJoules~cm z. For visible light curing, in order to initiate the polymerization of the ethylenically unsaturated monomer, the make coat precursor should be exposed to an energy :level of at least between 100 to 700 milliJoules~crri 2, preferably between 400 to 600 milli3oules~crri 2.
In order to fully cure the ethylenically unsaturated monomer, the make coat precursor is exposed to an energy source. This energy source during the fabrication of the coated abrasive article of the present invention can be thermal, which includes both infrared and heat, or radiation energy, which includes electron beam, ultraviolet light or visible light. The ethylenically unsaturated monomer polymerizes via a free radical mechanism. For the thermal, ultraviolet light and visible light energy sources, a curing agent is required for the ethylenically unsaturated monomer for the polymerization to begin. The time and the amount of energy required to fully polymerize depends upon the actual ethylenically unsaturated monomer, type of curing agent for the ethylenically unsaturated monomer, and the density and thickness of the make coat precursor. It is preferred, during this full curing step, to minimize the amount of oxygen present.
One means to accomplish this, is to cure the precursor in a nitrogen atmosphere.
Another means is to knife-coat the make coat precursor and cover the make coat precursor with a transparent polymeric film. The curing steps) are then done with the polymeric film over the make coat precursor. If a polymeric film is used, the film needs to be removed prior to application of the abrasive grains.
In the first method for making a coated abrasive article of the present invention, it is preferable that (1) the make coat is applied to a backing, (2) then exposing the make coat to an energy source to activate the cationically polymerizable monomer or polyurethane precursor initiator, (3) partially polymerizing, either sequentially or simultaneously, the cationically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer;
or both, and (4) then applying a plurality of abrasive grains. Advantageously, applying a size coat precursor, and fully curing both the make coat precursor and the size coat precursor may be accomplished in any order. For example, the make coat precursor could be fully cured prior to application of the size coat precursor and subsequent full cure of the size coat precursor. Alternatively, the size coat precursor can be coated over the layer of abrasive grains and then both the size coat precursor and the make coat precursor are fully cured. Partially polymerizing the make coat precursor prior to the application of abrasive grains, permits a substantially monolayer of grains. The partially polymerized make coat precursor is a pressure-sensitive adhesive like layer. The layer has sufficient "tack"
to hold the abrasive grains during application and curing of the size coat, resulting in a substantially monolayer of abrasive grains. The degree of "tack" can vary with the size of the grain. For example, a large abrasive grain will generally require a greater degree of tack than a small abrasive grain. One advantage of the present invention is that the make coat precursor layer, once partially polymerized is sufficiently tacky to hold the abrasive grains and does not display a viscosity that will wet and wick up the abrasive grains.
In the second method for making a coated abrasive article of the present invention, (1) the make precursor is applied to a backing, (2) the make coat precursor is then exposed to an energy source to fully cure the precursor, (3) a plurality of abrasive grains are applied, and (4) a size coat is applied and cured.
The make coat, although fully polymerized, is a pressure sensitive adhesive, typically having the properties of (1) being tacky, (2) exerting a strong holding force, (3) having sufficient cohesiveness and elasticity that it can be removed from smooth surfaces without leaving a visible residue, and (4) requiring no activation by water, solvent or heat to become tacky. The make coat has sufficient "tack"
to hold the abrasive grains during the application and curing of the size coat. The degree of '°tack" can vary with the size of the grain. For example, a Iarge abrasive grain will generally require a greater degree of tack than a small abrasive grain. One advantage of the present invention is that the make coat precursor layer, once polymerized is sufficiently tacky to hold the abrasive grains and does not display a viscosity that will wet and wick up the abrasive grains. It is contemplated that any viscoelastic material that in solvent-free form remains permanently tacky and adheres instantaneously to most solid surfaces with the application of very slight pressure would be within the scope and prinicples of the present invention. Such pressure-sensitive adhesives are recognized as possessing a "four-fold balance" of adhesion, cohesion, stretchiness, and elasticity. See Houwink and Salomon, Adhesion and Adhesives (Elsevior Publishing Co. 1967).
In the preferred embodiment of the second method for making a coated abrasive article of the present invention, it is preferable that (1) the make coat is applied to a backing, (2) then exposing the make coat to an energy source to activate, either sequentially or simultaneously, the cationically polymerizable monomer or the polyurethane precursor; the ethylenically unsaturated monomer;
or both, (3) fully curing the make coat precursor, (4) then applying a layer of abrasive grains, (5) applying a. size coat precursor of the layer of abrasive grains and (6) fully curing the size coat precursor. In order to have a make coat with this pressure sensitive adhesive properties, the proper selection of the ethylenically unsaturated monomer and either the cationically polymerizable monomer or the polyurethane precursor is beneficial. Typically, the ethylenically unsaturated monomer will be predominantly monofunctional, and the canonically polymerizable monomer, preferably cycloaliphatic epoxy monomers, and polyurethane will have a functionality greater than 2 on the average. It is generally preferred that the size coat precursor be cured upon application to prevent penetration of the size coat precursor into the fully cured make coat.
Objects and advantages of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention.

Examples All coating weights are specified in grams/square meter. All formulations ratios are based upon parts by weight.
All materials are commerically available or known in the literature unless otherwise stated or apparent.

GLOSSARY

IOA isooctyl acrylate NVP N-vinyl pyrrolidone PH1 2,2-dimethoxy-1,2-diphenyl-1-ethanone (Irgacure'"' 651, commerically available from Ciba-Geigy, or KB-1 commercially available from Sartomer) HPA 2,2,-bis-4-(2-hydroxyethyoxyphenyl)hexafluoropropane (hydroxyethylated bisphenol A) HDODA 1,6-hexanediol diacrylate PH2 eta6-(xylenes (mixed isomers))-eta5-cyclopentadienyl iron (1+) hexafluorophosphate TEGDA tetraethylene glycol diacrylate (commercially available from Sartomer under the trade designation "SR-268") BDDA butanediol diacrylate (commercially available from Sartomer under the trade designation "SR-313") PUPl a biuret of 1,6-hexamethylene diisocyanate (commercially available from Mobay Corp. under the trade designation "Desmodur let-100") IPDI isophorone diisocyanate EM1 bis-(3,4-epoxy-6-methylcyclohexylrnethyl) adipate (commercially available from Union Carbide under the trade designation ERL 4229) PH3 eta6-(xylenes . (mixed isomers))-eta5-cyclopentadienyliron(1+) hexafluoroantinomate RP1 a resole phenolic resin (70% solids in water/2-ethoxy ethanol) RP2 a resole phenolic resin (75 % solids in water/2-ethoxy ethanol) r p ~~ ~~''~' 2J' ~~ 5f-1 hd PP a polyester resin (a plasticizes for the resol phenolic resin) BA n-butyl acrylate THFA tetrahydrofurfuryl acrylate (commerically available from Sartomer under the trade designation "SR-285") EM2 a bisphenol A epoxy resin (commercially available from Shell Chemical under the trade designation '°Epon 828" -epoxy equivalent wt. of 185-192 g~eq-1) EM3 a bisphenol A epoxy resin (commercially available from Shell Chemical under the trade designation "Epon 1001F" -epoxy equivalent wt. of 525-550 g~eq-1) tBOX di-t-butyl oxalate EM4 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate (commercially available from Union Carbide under the trade designation "ERL 4221 ") PH4 eta~-(cumene)-etas-cyclopentadienyliron (1+) hexafluorophosphate (commercially available from Ciba-Geigy under the trade designation "Irgacure 261 ") WA a wetting agent (commercially available from Akzo Chemie America Interstab Chemicals under the trade designation "Interwet 33") The following test procedures were used to test the coated abrasive made according to the examples.
DISC TEST PROCEDURE I
The coated abrasive article was converted into a 10.2 cm diameter disc and secured to a foam back up pad with a pressure sensitive adhesive. The coated abrasive disc and back up pad assembly was installed on a Schiefer testing machine and the coated abrasive disc abraded "PLEXIGLAS" (polymethyl methacrylate).
The load was 4.5 kg. All of the testing was done underneath a water flood. The total amount of "PLEXIGLAS°° removed and the surface finish (Ra and Rtm) of the plexiglass workpiece were measured at various revolutions or cycles of the coated abrasive disc. "Ra" is the arithmetic average of the scratch size in microinches. "Rtm" is the average measured over five consecutive sampling . ,~s G, ~yp "~) ~( 2 3J i,I :r.d d - 34 - s, ;'3 t3 ~3 lengths of the maximum peak to valley height in each sampling length. In some instances the surface finish was not measured.
DISC TEST PROCEDURE II
The Disc Test Procedure II follows Disc Test Procedure I, except the grinding was done dry, that is, no water flood.
DISC TEST PROCEDURE III
The coated abrasive article was converted into a 7.S cm diameter disc and secured to a foam back up pad with a pressure sensitive adhesive. The coated abrasive disc and back up pad assembly was installed on a Schiefer testing machine. The coated abrasive disc abraded a 1018 mild steel ring workpiece having a 10.2 cm outer diameter and a 6.4 cm inner diameter. The load was 4.5 kg. All of the testing was done dry, that is, no water present. The total amount of mild steel removed was measured at various revolutions or cycles of the coated abrasive disc.
DISC TEST PROCEDURE IV
The Disc Test Procedure IV follows Disc Test Procedure I, except that the coated abrasive was converted into a 7.6 cm diameter disc. Additionally, the workpiece was a ring having a 10.2 cm outer diameter and a S.1 cm inner diameter.

Into a glass jar were charged and thoroughly mixed with a magnetic stirrer 80 parts IOA, 20 parts NVP and 0.04 part PHI. The resulting mixture was then degassed to remove oxygen by bubbling nitrogen gas through the solution for at least five minutes. The mixture was then exposed to a Black-Ray lamp for about 45 seconds to prepolymerize the materials to a viscosity between 1000 to 3000 centipoise, using a Brookfield viscometer with a No. LV2 spindle at a rotation setting of 6, at 21 °C. The resulting material was designated FA.

Into a glass jar were charged and thoroughly mixed with a magnetic stirrer 36 parts BA, 24 parts THFA and 0.024 part PH1. The resulting mixture was then degassed to remove oxygen by bubbling nitrogen gas through the solution for at least five minutes. The mixture was then exposed to a Black-Ray lamp for about 45 seconds to prepolymerize the materials to a viscosity about 2000 centipoise, using a Brookfield viscometer with a No. LV2 spindle at a rotation setting of 6, at 21 °C. The resulting material was designated FB.
lO PREPARATION EXAMPLE 3 The material was prepared according to Preparation Example l except 70 parts IOA, 15 parts NVP, and 0.04 part PH1 were charged into the glass jar.
The resulting material was designated FC.

The material was prepared according to Preparation Example 1 except 100 parts IOA and 0.04 parts PH1 were charged into the glass jar. The resulting material was designated FD.

This set of Examples compared various make coat precursor formulations.
The resulting coated abrasives were tested according to the Disc Test Procedure I and the results are summarized in Table 1.

A make coat precursor was prepared by thoroughly mixing 85 parts of FA
and 15 parts HPA at 80°C. Then 0.1 part of HDODA, 0.1 part of PH1 and 0.05 part of PH2 were thoroughly mixed into the make coat precursor. Just prior to coating, the make coat precursor was heated in a water bath at 90°C.
Next, 7.5 parts of PUP1 and 7.5 parts of IPDI were then thoroughly mixed into the make coat precursor. The resulting make coat precursor was degassed under vacuum in a desiccator to remove air bubbles and dissolved oxygen. The make coat y °al ~~

precursor was then knife-coated to a thickness of 0.05 millimeters (mm) onto an A weight waterproof paper. A release-coated polyester film cover sheet was placed over the make coat precursor during knife-coating and subsequent processing. The make coat precursor was then irradiated at U.5 meters/minute (m~miri 1) with two 300 Watt flood lights followed by 600 milliJoules/cm2 (mJ~cni 2) of ultraviolet light. The cover sheet was then removed and grade 600 silicon carbide abrasive grain was drop coated into the make coat precursor. The abrasive grain layer had an average weight of 17 gnri 2. The resulting product was thermally cured at 100°C for about 10 minutes. Subsequently, a size coat precursor was sprayed over the abrasive grains. The size coat precursor had an average weight of 8 gnri 2. The size coat precursor was 30% solids in ethanol of a 90:10 ratio of RPl:PP. The resulting product was precured for one hour at 88°C and final cured for about 90 minutes at 115°C.

A coated abrasive was prepared according to Example 1 except the make coat precursor was 80 parts of FD, 20 parts of EM1, 1 part of PH1, 0.5 part of PH3 and 0.1 part of HDODA.

Comparative Example 1 was a grade 600 Tri-M-ite Wetordry Type W
coated abrasive (commercially available from the 3M Co., St. Paul, MIA.

The coated abrasive was prepared according to Example 1 except the make coat precursor was 80 parts of FA, 1 part of PHl and 0.1 part of HDODA.

- ~~~v Example No, of CyclesCumulativeSurface Finish Cut (g) (Ra/Rtm) 500 0.998 10/58 1 1000 1.615 8/46 2000 2.195 5/30 500 1.191 10/63 2 1000 2.094 9/56 2000 3.155 7/49 500 fl.958 12/68 C1 1000 1.781 9/60 2000 2.773 8/50 500 0.754 8/43 C2 1000 1.206 5/30 2000 1.589 4/30 This set of Examples compared various coated abrasive constructions. The resulting coated abrasives were tested according to the Disc Test Procedure IV
and the results are summarized in Table 2.

The make coat precursor was prepared according to Example l and applied to a backing in a similar manner as described in Example 1. The make coat precursor was irradiated at 0.5 m~miri 1 with visible light using four bulbs from a copying machine. The temperature underneath these bulbs was approximately 90°C. After the exposure to the visible light, the make coat precursorlbacking was heated for 5 minutes at 90°C, followed by exposure to 600 mJ~crn'2 of ultraviolet light. The cover sheet was then removed and grade 600 silicon carbide abrasive grain was electrostatically coated into the make coat precursor. The abrasive grain layer had an weight of 13 g~m 2. The resulting product was thermally cured at 100°C for about 10 minutes. A size coat precursor was sprayed over the abrasive grains. The size coat precursor had an average weight E.u a~ ~y~ 2 of 15 g~m 2. The size coat precursor was 30% solids in ethanol of a 90:10 ratio of RP1:PP. The resulting product was precured for one hour at 88°C and final cured for about 90 minutes at 115°C.

A make coat precursor was prepared by thoroughly mixing the contents of FB 60 parts with 20 parts of EM2, 20 parts of EM3, 4 parts of cyclohexanedimethanol, 1 part of PHl, 1 part of PH3 and 1 part of tBOX. The resulting make coat precursor was degassed. The make coat precursor was then knife-coated to a thickness of 0.5 mm onto an A weight waterproof paper. A
release-coated polyester film cover sheet was placed over the make coat precursor during knife-coating and subsequent processing. The make coat precursor was then irradiated with 600 mJ~crri Z of ultraviolet light. The cover sheet was removed and grade 600 silicon carbide abrasive grain was electrostatically coated into the make coat precursor. The abrasive grain layer had an average weight of 13 g~m 2. The size coat used was the same as described in Example 1. The coated abrasive article was then precured and cured according to the procedures of Example 1.

A coated abrasive article was prepared according to Example 4 except the size coat was prepared with 90 parts of EM4, 10 parts of HDODA, 0.25 part of PH3 and 0.25 part of PH1. The size coat was diluted to 70% solids in methyl ethyl ketone (MEI~) and sprayed over the abrasive grains/make coat precursor.
The size coat had an average coating weight of 15 gwi 2. The size coat precursor was then exposed to a 120 Watts-cni 1 ultraviolet light (Fusion System D bulb) at 3 m~miri 1 for a total of three times. The resulting coated abrasive was thermally cured for about 15 minutes at 100°C.

y ,. ;r Example No. of CyclesCumulative Surface Finish Cut (g) Ra/Rtm 500 0.727 11/72 C 1 10013 1.266 ---1500 1.692 ---2000 2.015 6/39 500 0.733 17/112 3 1000 1.330 ---1500 1.841 ---2000 2.264 11/71 500 0.911 21/137 4 1000 1.614 ---1500 2.313 ---2000 2.841 11/80 500 0.881 12/78 5 1000 1.632 ---1500 2.282 ---2000 2.854 8/50 Surface finish was not measured for these cycles.

This set of Examples compared various coated abrasive constructions. The resulting coated abrasives were tested according to the Disc Test Procedure II
and the results are summarized in Table 3.

A make coat precursor was prepared with FC 85 parts, 1 park PH4, 0.03 part PH3, 0.1 part HDODA and 15 parts of ethoxylated bisphenol A. Just prior to coating, the make coat precursor was heated in a water bath at 90°C.
Next, 7.S
parts of PUP1 and 7.5 parts of IPDI were then thoroughly mixed into the make coat precursor. The resulting make coat precursor was degassed under vacuum in a desiccator to remove air bubbles and dissolved oxygen. The make coat precursor was then knife-coated to a thickness of 0.05 mm onto a D weight Kraft paper. Prior to coating, the knife-coater was heated with infrared lamps to a ~ w ::' ~'~ j '~
i~ ~~ e~ ~ .,r Na temperature between 70 to 90°C for about 30 minutes. A release-coated polyester film cover sheet was placed over the make coat precursor during knife coating and subsequent processing. The make coat precursor was irradiated at 0.5 m~miri 1 with two 120 Watt ~crri 1 flood lights placed approximately 5 cm above the release film. Following this, the make coat precursor was irradiated with ultraviolet light for a total energy exposure of about 600 milli~oules~crti 2. The cover sheet was then removed and grade 400 aluminum oxide abrasive grain was drop coated into the make coat precursor. The abrasive grain layer had an average weight of about 45 g~m-2. The resulting product was thermally cured at 100°C for 15 minutes.
Subsequently, a size coat precursor was sprayed over the abrasive grains. The size coat precursor was a 90:10 ratio of RP1:PP with 1 % WA. The size coat precursor was diluted to 20% solids with a 50:50 blend of ethanol and ethylene glycol monoethyl ether. The resulting product was precured for one hour at 88°C
and final cured for 90 minutes at 120°C.

A coated abrasive was prepared according to Example 6 except the ethoxylated bisphenol A was replaced with the hydroxyethylated bisphenol of methylethylketone. Further, the abrasive grain coating weight was about 39 gwf EJiAMPLE 8 A coated abrasive was prepared according to Example 7 except the release liner was removed after the visible light irradiation (floed lights) and the abrasive grains were drop-coated into the make coat. The abrasive grain coating had an average weight of 43 g~rri 2. The make coat precursor/abrasive grains were then irradiated with ultraviolet light.

Comparative Example 3 was a grade 400 Production Wetordry Paper Type T2 coated abrasive (commercially available from the 3M Company, St. Paul, 14IN). The backing for this coated abrasive was an A weight waterproof paper.

c a'.. t? p'~~'~(/~
'.L" ~ s ~ ~ ~8 The abrasive grain was fused aluminum oxide.

Example No. of CyclesCumulative Surface Finish Cut (g) RalRtm 500 1.113 13/82 6 2000 3.346 12/68 4000 5.029 11/64 500 1.154 14/82 7 2000 3.260 11/70 4000 5.501 11/68 500 1.130 16/ 104 8 2000 3.600 13/82 4000 6.292 12172 500 0.737 10166 C3 2000 1.856 12/64 4000 2.538 9/49 This set of Examples compared various coated abrasive constructions. The resulting coated abrasives were tested according to the Disc Test Procedure III and the results are summarized in Table 4.

A make coat precursor was prepared with FB 60 parts, 20 parts of EM2, 20 parts of EM3, 4 parts of cyclohexanedimethanol, 1 part of PH1, 1 part of and 1 part of tBOX. The make coat precursor was degassed under vacuum in a desiccator to remove air bubbles and dissolved oxygen. Then, the make coat precursor was knife-coated to a thickness of 0.05 mm onto 0.13 mm thick polyester film previously primed with an ethylene acrylic acid copolymer. A
release-coated polyester film cover sheet was placed over the make coat precursor during knife-coating and subsequent processing. The make coat precursor was then irradiated with 600 mJ~cm 2 of ultraviolet light. The cover sheet was then ~,~'~~yG~~~'s;~
_42_ removed and ,grade P120 aluminum oxide abrasive grain was electrostatically coated into the make coat precursor. The abrasive grain layer had an average weight of 190 gwi 2. The resulting product was thermally cured at 100°C
for 1S
minutes. Subsequently, a size coat precursor was sprayed over the abrasive grains. The size coat precursor was prepared using 48 % RP2 and 52 % calcium carbonate filler, The size coat precursor was diluted to 70% solids with a 90:10 water:2-ethoxy ethanol solvent. The size coat precursor coating weight was 110 g~m 2. The resulting product was precured for about 90 minutes at 90°C, final cured for 10 hours at 100°C and post cured for about 30 minutes at 116°C. After this curing the coated abrasive was flexed.
EXAMPLE lO
A coated abrasive was prepared according to Example 9 except the size coat precursor coating weight was 170 g~rri 2.

A coated abrasive was prepared according to Example 9 except the size coat precursor coating weight was 200 g~m 2.

A coated abrasive was prepared according to Example 9 except the make coat precursor was prepared using 60 parts of FB, 20 parts of EM2, 20 parts of EM3, 4 parts of 1,4-cyclohexane dimethanol, 1 part of FH1, 1 part of PH3, 0.08 parts of HDODA and 1 part of tBOX. The size coat precursor coating weight was 150 g~m 2.

A coated abrasive was prepared according to Example 9 except the make coat precursor was prepared using 60 part of FB, 20 parts of EM2, 20 parts of EM3, 4 parts of 1,4-cyclohexane dimethanol, 1 part of PHI, I part of PH3, 5 parts of glycidyl acrylate and 1 part of tBOX. The size coat precursor coating weight was 150 g~m 2.

- 43 - ~ i.3 ~ ~ ~ ~ ~a COIVtPARATIVE EXAMPLE 4 Comparative Example 4 was a grade P120 Three-M-ite Resin Bond film closed coat coated abrasive (commercially available from the 3M Co., St. Paul, MIA.

Example 110. of CyclesCumulative Cut (g) 500 0.339 1000 0.505 9 1500 O.S99 2000 0.669 2500 0.723 500 0.448 1000 0.642 10 1500 0.758 2000 0.843 2500 0.905 500 0.469 1000 0.713 I5 11 1500 0.844 2000 0.944 2500 1.020 500 0.400 1000 0.564 I2 1500 0.658 2000 0.734 2500 0.799 500 0.455 1000 0.656 13 1500 0.744 2000 0.860 2500 0.931 500 0.510 1000 0.751 C4 1500 0.894 2000 0.977 2500 1.049 EXAMPLES 14 Arrn 15 This set of examples compared the performance of coated abrasives in which polymerization of the make coat precursor was initiated before and after the ~.~ c~
~~4~t3~)~~ a abrasive grains were applied. The coated abrasives were tested under Test Procedure III and the results are summarized in Table 5.

A make coat precursor was prepared by thoroughly mixing the contents of FB 50 parts with 20 parts of EM2, 20 parts of EM3, 4 parts of 1,4-cyclohexane dimethanol, 0.5 part of PH1, 0.5 part of PH3 and 0.5 part of tBOX. The resulting make coat precursor was degassed under vacuum. The make coat precursor was knife-coated to a thickness of 0.05 mm onto a polyester film previously primed with an ethylene acrylic acid copolymer. The make coat precursor was irradiated under a nitrogen atmosphere by passing the coated film under two 80 Watts~crri i mercury lamps four times at 15 m~miri 1. Grade 1000 JIS white aluminum oxide was drop coated into the make coat precursor. The abrasive grain layer had an average weight of 15 gW 2. The resulting product was thermally cured at 110°C
for 15 minutes. The remaining steps to prepare the coated abrasive were the same as Example b.

The backing, make coat precursor, and the abrasive grain were the same as Example 15. The make coat precursor was knife-coated onto the backing with a thickness of about 8 micrameters (~,m). The abrasive grain weight was about gnri 2. After the abrasive grains were applied, polymerization of the make coat precursor was initiated by exposing the resulting material under a nitrogen atmosphere to two 80 Watts~crri 1 mercury Lamps four times at 15 m~miri 1. The resulting product was thermally cured at 110°C for 15 minutes. The remaining steps to prepare the coated abrasive were the same as Example 6. The abrasive grain coating was very blotchy.

) ~~~J~J

Example No. of Cycles Cumulative Cut (g) 500 0.41 1000 0.77 14 1500 1.13 2000 1.37 2500 1.63 500 0.31 1000 0.53 15 1500 0.75 2000 0.89 2500 1.03 Examples 14 and 15, the surface finish (500 cycles) Ra/Rtm was 6/43 and 8/45, respectively.

This set of Examples compared various coated abrasive constructions. The resulting coated abrasives were tested according to the Disc Test Procedure II
and Disc Test Procedure III and the results are summarized in Tables 6 and 7.
EXrIMPLE 16 The coated abrasive for Example 16 was made in the same manner as Example 9 except that the make coat precursor thickness was 0.10 millimeters and the size coat precursor coating weight was 205 gnri 2.

The coated abrasive for Example 17 was made in the same manner as Example 9 except that the make coat precursor thickness was 0.20 millimeters and the size coat precursor coating weight was 197 g~rri 2.

4"
~'~~1~~~

The coated abrasive for Example 18 was made in the same manner as Example 9 except that the make coat precursor thickness was 0.025 millimeters and the size coat precursor coating weight was 205 gwi 2. Additionally, the make coat precursor further contained 0.5 part of tBOX.

The coated abrasive for Example 19 was made in the same manner as Example 9 except that the make coat precursor further contained 0.5 part of tBOX
and the size coat precursor Boating weight ryas 205 gW z.

The coated abrasive for Example 20 was made in the same manner as Example 9 except that the make coat precursor thickness was 0.10 millimeters and the size coat precursor coating weight was 200 g~m 2. Additionally, the make coat precursor further contained 0.5 part of tBOX.

The coated abrasive for Example 21 was made in the same manner as Example 20 except that a different size coat precursor was employed. The size coat consisted of 50% by weight alumina trihydrate filler and 50% by weight of an epoxy resin formulation. The epoxy resin formulation was diluted with MEK
solvent to 75 % solids. The epoxy resin formulation consisted of 90 parts EM4, 10 parts HDODA, 0.25 part PH1 and 0.25 part PH4. After the size coat precursor was sprayed over the abrasive grains, the resulting coated abrasive article was exposed to four ultraviolet Lamps operating at 150 Watts~cW 1 with a run speed of 4.5 m~min-1. The coated abrasive was then thermally cured for one hour at 100°C.

~r~4~~~;~'~'~~
;cd 7,tX ~ 'tl J

Example No. of Cycles Cumulative Cut (g) 50p 0.96 1000 1.88 11 1500 2.65 2000 3.48 2500 4.28 500 1.27 1000 2.54 21 1500 3.65 2000 4.72 2500 5.74 Spp 1.24 1000 2.38 C4 1500 3.50 2000 4.61 2500 5.64 Example No. of CyclesCumulative Cut (g) 500 O.SO

S 1000 0.73 9 1500 0.85 2000 0.94 2500 1.02 500 0.48 1000 0.67 16 1500 0.76 2000 0.82 2500 0.88 500 0.48 1000 0.68 17 1500 0.82 2000 0.90 2500 0.94 500 0.53 1000 0.72 18 1500 0.84 2000 0.92 2500 0.98 500 0.48 1000 0.64 19 1500 0.73 2000 0.79 2500 0.85 500 0.50 1000 0.70 20 1500 0. 83 2000 0.91 2500 0.95 S00 0.56 1000 0.83 C4 1500 0.93 2000 1.01 2500 1.07 r This set of Examples compared various coated abrasive constructions. The resulting coated abrasives were tested according to the Disc Test Procedure IV
S and Disc Test Procedure I and the results are summarized in Table 8.

This example describes a 600 grit abrasive construction with an epoxy-acrylate make coat which was polymerized with high intensity UV light at a high web rate in air. A make coat precursor was prepared by using a stock solution of EM2/EM3(80:20) made by mixing 480 parts EM2 and 120 parts EM3, heating in an oven at 80°C and shaking until it was a homogeneous solution. To 160 parts of this solution, were added 20 parts TEGDA, 20 parts BDDA, 16.07 parts 1,4-cyclohexane dimethanol, 1.0 part PH3, 1.0 part tBOX, and 1.0 part PH1 (KE-1).
1S This mixture was heated in an oven at 60°C until homogeneous and then stored in the dark at room temperature until used. This solution was knife coated at SO
~.m thickness onto 100 ~,m polyester film. It was exposed to high intensity UV
light operating at 120 Watts~crri 1 with a run speed of about 24 m~miri 1.
Grade 600 silicon carbide abrasive grain was drop-coated into the make coat such that the film was completely covered with abrasive grains to substantially a mono-layer thickness. The resulting product was thermally cured at 100°C for about minutes. The size coat precursor was the same as described in Example S. The coated abrasive article was then precured and cured according to the procedures of Example S.

This example describes a 1200 grit abrasive constnrction with an epoxy-acrylate make coat which was polymerized~with high intensity UV light at a high web rate in air. The make coat precursor was prepared using a stock solution of EM2/EM3 (50:50) made by mixing 2S0 parts EM2 and 2S0 parts EM3, heating in an oven at 80°C and shaking until it was a homogeneous solution. To 75.33 parts of this solution were added 19.83 parts TEGDA, 5.84 parts 1,4-%. ~) Y.~ F~ : j :~
c~,t,:~~3',iwG.~r~

cyclohexanedimethanol, 1.0 part PH1, 1.0 part tBOX and 1.0 part PH3. This mixture was heated at 60°C until all ingredients were in solution, then stored in the dark at room temperature until used. This solution was knife coated at 50p.m thickness onto 100 ~cm polyester film. It was exposed to high intensity UV
light S operating at 80 Watts~cW 1 with a run speed of about 15 m-miri 1. Grade 1200 silicon carbide abrasive grain was drop-coated onto the make coat, such that the film was completely covered with abrasive grains to substantially a mono-layer thickness. The resulting product was thermally cured at 100°C for about minutes. The size coat precursor was the s<~me as described in Example 5. The coated abrasive article was then precured and cured according to the procedures of Example 5.

A make coat precursor was prepared by thoroughly mixing 60 parts EM2, 32 parts IOA, 8 parts HDODA, 0.4 part PH3, 0.4 part tBOX, 2 part PH1. The make coat precursor was roll-coated onto an A weight waterproof paper at a coating weight of 4 gnrfl. The make coat precursor was then irradiated with milliJoules~cm 2 of ultraviolet light in air. Grade 1220 silicon carbide abrasive grain was then coated electrostatically into the make coat precursor. The abrasive ' 20 grain layer had an average weight of 14.5 g~m 2. The resulting product was thermally cured at 115°C for 10 minutes. The size coat precursor was identical to Example S except it was diluted to 90% solids with toluene. It was roll-coated onto the abrasive product to a coating weight of 8 gW 2. subsequently, it was irradiated at 10 m~miri 1 with a 120 Watt/cm ultraviolet lamp. The resulting coated abrasive was thermally cured for 60 minutes at 115°C.
COMPARATIVE EXAPVlPLE S
Comparative Example 5 was a grade 1200 Tri-M-ite Wetordry Type W
coated abrasive (commerically available from the 3M Co., St. Paul, MIA.

Table 8 Example No, of Cycles Cumulative Cut (g) 500 0.994 10(~ 1.865 22 15~ 2.627 2000 3.366 2500 4.050 500 0.590 1000 0.981 C 1 1500 1.274 (IV) 2000 1.518 2500 1.916 500 0.574 lppp 1.039 23 1500 1.509 2000 1.870 2500 2.220 500 0.199 1000 0.280 C5 1500 0.280 2ppp 0.319 2500 0.370 500 0.713 1000 1.153 24 1500 1.618 (I) 2ppp 2.042 2500 2.380 __5~ 0.379 1000 0.617 C5 1500 0.829 (I) 2~0 0.920 2500 1.021 Various modifications and alterations of this invention will become apparent to those sltilled in the art without departing from the Scope and spirit of this invention, and i~t should be understood that this invention is not to be unduly limited to the illustrative embodiments set forth herein.

Claims

1. A method for making a coated abrasive article comprising the steps:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises:
(a) at least one ethylenically unsaturated monomer, and (b) one or both of a cationically polymerizable monomer and a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
at least one cationically polymerizable monomer or polyurethane precursor initiator;
(2) exposing the make coat precursor to an energy source to activate the organometallic complex salt;
(3) partially polymerizing the one or both of the cationically polymerizable monomer and the polyurethane precursor; and the ethylenically, unsaturated monomer, either sequentially or simultaneously;
(4) applying a plurality of abrasive grains into the make coat precursor;
(5) applying a size coat precursor;
(6) fully curing the make coat precursor; and (7) fully curing the size coat precursor.

2. The method according to claim 1, wherein the make coat precursor comprises the cationically polymerizable monomer as component (b) and wherein the curing agent further comprises at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with a metal ion of an organometallic complex salt.

3. The method according to claim 1 or 2, wherein the curing agent further comprises at least one free radical initiator.

4. The method according to any one of claims 1 to 3, wherein the cationically polymerizable monomer of the make coat precursor is partially cured prior to applying the plurality of abrasive grains and then the make coat precursor is fully cured.

5. The method according to claim 4, wherein the size coat precursor is applied before the make coat precursor is fully cured.

6. The method according to claim 4, wherein the size coat precursor is applied after the make coat precursor is fully cured.

7. The method according to any one of claims 1 to 3, wherein the ethylenically unsaturated monomer of the make coat precursor is partially cured prior to applying the plurality of abrasive grains and then the make coat precursor is fully cured.

8. The method according to claim 7, wherein the size coat precursor is applied before the make coat precursor is fully cured.

9. The method according to claim 7, wherein the size coat precursor is applied after the make coat precursor is fully cured.

10. The method according to any one of claims 1 to 9, wherein the plurality of abrasive grains is substantially a monolayer.

11. A method for making a coated abrasive article comprising:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises a pressure sensitive adhesive precursor;
(2) fully cursing the make coat precursor to a pressure sensitive adhesive;
(3) applying a plurality of abrasive grains into the cured make coat;
(4) applying a size coat precursor; and (5) fully curing the size coat precursor.

12. A method for making a coated abrasive article comprising:
(1) applying a make coat precursor to a backing, wherein the make coat precursor comprises:
(a) at least one ethylenically unsaturated monomer, and (b) one or both of a cationically polymerizable monomer and a polyurethane precursor, and (c) a catalytically-effective amount of a curing agent comprising:
at least one cationically polymerizable monomer or polyurethane precursor initiator;

(2) exposing make coat precursor to an energy source to activate the one or both of the cationically polymerizable monomer and the polyurethane precursor; and the ethylenically, unsaturated monomer, either sequentially or simultaneously;
(3) fully curing the make coat precursor;
(4) applying a plurality of abrasive grains into the make coat precursor. ;
(5) applying a size coat precursor; and (6) fully curing the side coat precursor.

13. The method according to claim 12, wherein the make coat precursor comprises the cationically polymerizable monomer as component (b) and wherein the curing agent further comprises at least one thermally decomposable ester reaction product of a tertiary alkyl alcohol and an acid that forms a chelation complex with the metal ion of the organometallic complex salt.

14. The method according to claim 12 or 13, wherein the curing agent further comprises at least one free radical initiator.

15. The method according to any one of claims 12 to 14, wherein the ethylenically unsaturated monomer is selected from the group consisting of acrylates, methacrylates, acrylamides, methacrylamides and vinyl compounds.

16. The method according to any one of claims 12 to 15, wherein the cationically polymerizable monomer undergoes cationic polymerization and includes 1,2-, 1,3-, and 1,4-cyclic ethers, and vinyl ethers.

17. The method according to any one of claims 12 to 16, wherein the polyurethane precursor is a mixture of one or more monomers including polyisocyanates and one or more polyol, or monomers bearing at least two isocyanate-reactive hydrogen atoms and such that the ratio of isocyanate groups to isocyanate-reactive hydrogens atoms is 1:2 to 2:1.

18. The method according to any one of claims 12 to 17, wherein the plurality of abrasive grains is substantially a monolayer.

19. A coated abrasive article comprising:
(1) a backing;
(2) a make coat layer on one surface of the backing, wherein the make coat layer comprises the polymerized product of:
(a) at least one ethylenically unsaturated monomer, (b) at least one cationically polymerizable monomer, (c) at least one organometallic complex salt, and (d) at least one thermally decomposable ester reaction product of a tertiary alcohol and an acid that forms a chelation complex with the metal ion of the organometallic salt;
(3) a plurality of abrasive grains on the surface or partially embedded into the surface of the make coat layer;
and (4) a size coat layer coated over the plurality of abrasive grains and the make coat layer.

20. The coated abrasive article according to claim 19, wherein the make coat layer comprises the polymerized product of components (a) to (d) and additionally (e) a peroxide.

21. The coated abrasive article according to claim 19 or 20, wherein the cationically polymerizable monomer is selected from the group consisting of diglycidyl ether of bisphenol A, bisphenol A epoxy resin, 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate, and bis-(3,4-epoxy-6-methylcyclohexylmethyl)adipate.

22. The coated abrasive article according to any one of claims 19 to 21, wherein the ethylenically unsaturated monomer is selected from the group consisting of monofunctional or polyfunctional acrylates, methacrylates, acrylamides, methacrylamides and vinyl compounds.

23. The coated abrasive article according to claim 22, wherein the ethylenically unsaturated monomer is selected from the group consisting of isooctyl acrylate, 1,6-hexanediol diacrylate, butyl acrylate, and tetrahydrofurfuryl acrylate.

24. The coated abrasive article according to claim 23, wherein the organometallic complex salt is represented by the following formula:
I (L1) (L2) M P] +q Yn wherein Mp represents a metal selected from the group consisting of Cr, Mo, W, Mn Re, Fe, and Co;
L1 represents 1 or 2 ligands contributing pi-electrons that can be the same or different ligand selected from the group of: substituted and unsubstituted eta3-allyl, eta5-cyclopentadienyl, and eta7-cycloheptatrienyl, and eta6-aromatic compounds selected from eta6-benzene and substituted eta6-benzene compounds and compounds having 2 to 4 fused rings, each capable of contributing 3 to 8 pi-electrons to the valence shell of M p;

L2 represents none, or 1 to 3 ligands contributing an even number of sigma-electrons that can be the same or different ligand selected from the group of: carbon monoxide, nitrosonium, triphenyl phosphine, triphenyl stibine and derivatives of phosphorus, arsenic and antimony, with the proviso that the total electronic charge contributed to M p results in a net residual positive charge of q to the complex;

q is an integer having a value of 1 or 2, the residual charge of the complex cation;

Y is a halogen-containing complex anion selected from BF4-, AsF6-, PF6-, SbF5OH-, SbF6-, and CF3SO3-; and n is an integer having a value of 1 or 2, the number of complex anions required to neutralize the charge q on the complex cation.

25. The coated abrasive article according to claim 24, wherein the thermally decomposable ester reaction product of a tertiary alcohol and an acid is selected from the group consisting of oxalic, phosphorous, and phosphoric acid.

26. The coated abrasive article according to claim 25, wherein the make coat layer comprises isooctyl acrylate, 1,6-hexanediol acrylate, bisphenol A epoxy resin, 2,2-dimethoxy-1,2-diphenyl-1-ethanone,eta6-xylenes-eta5-cyclopentadienyliron (1+) hexafluoroanintomate, or mixed isomers thereof, and di-t-butyl oxalate.

27. The coated abrasive article according to claim 26, wherein the size coat layer comprises 1,6-hexanediol acrylate, 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate, eta6-xylenes-etas-cyclpentadienyliron(1+)hexafluoroanintomate, or mixed isomers thereof, and 2,2-dimethoxy-1,2-diphenyl-1-ethanone.

28. A coated abrasive article comprising:
(1) a backing;
(2) a make coat layer on one surface of the backing, wherein the make coat layer comprises the polymerized product of:

(a) at least one ethylenically unsaturated monomer, (b) a polyurethane precursor, wherein when cured, the polyurethane has a glass transition temperature above room temperature;
(c) a polyurethane precursor initiator, and (3) a plurality of abrasive grains on the surface or partially embedded into the surface of the make coat layer;
and (4) a size coat layer coated over the plurality of abrasive grains and the make coat layer.

29. The coated abrasive article according to claim 28, wherein the polyurethane precursor is a mixture of one or more monomers including polyisocyanates and one or more polyol, or monomers bearing at least two isocyanate-reactive hydrogen atoms and such that the ratio of isocyanate groups to isocyanate-reactive hydrogen atoms is 1:2 to 2:1.

30. The coated abrasive article according to claim 29, wherein the polyurethane precursor comprises (1) a polyisocyanate, wherein the polyisocyanate is a biuret of 1,6-hexamethylene diisocyanate, or isophorone diisocyanate, or a mixture thereof, and (2) a polyol, wherein the polyol is hydroxyethylated bisphenol A.

31. The coated abrasive article according to any one of claims 28 to 30, wherein the ethylenically unsaturated monomer is selected from the group consisting of monofunctional or polyfunctional acrylates, methacrylates, acrylamides, methacrylamides and vinyl compounds.

32. The coated abrasive article according to claim 31, wherein the ethylenically unsaturated monomer is selected from the group consisting of isooctyl acrylate, N-vinyl pyrrolidone, N,N-dimethylacrylamide, 1,6-hexanediol diacrylate, butyl acrylate, and tetrahydrofurfuryl acrylate.