CA2255075C - Waterproof paper-backed coated abrasives - Google Patents
Waterproof paper-backed coated abrasives Download PDFInfo
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- CA2255075C CA2255075C CA002255075A CA2255075A CA2255075C CA 2255075 C CA2255075 C CA 2255075C CA 002255075 A CA002255075 A CA 002255075A CA 2255075 A CA2255075 A CA 2255075A CA 2255075 C CA2255075 C CA 2255075C
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- resin
- radiation
- paper
- coated abrasive
- maker
- Prior art date
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D11/00—Constructional features of flexible abrasive materials; Special features in the manufacture of such materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24D—TOOLS FOR GRINDING, BUFFING OR SHARPENING
- B24D3/00—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
- B24D3/02—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
- B24D3/20—Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
- B24D3/28—Resins or natural or synthetic macromolecular compounds
Abstract
Waterproof coated abrasive paper made using a maker and/or size coat comprising a radiation-curable binder that is hydrophobic when polymerized.< /SDOAB>
Description
CA 022~07~ 1998-11-16 RE~LAC~EM ~A~E;~
WATERPROOF PAPER-BACKED COATED ABRASIVES
Background to the Invention The present invention relates to the production of coated abrasives and particularly to the production of coated abrasives with a paper backing and more specifically to waterproof coated abrasives.
Such materials typically comprise a paper backing with the grain held by phenolic-modifed varnish resin maker and size coats. The use of the modified varnis'h as the bond renders the product waterproof. However it is found that such products require several hours to complete the cure of the binders and this therefore implies a very large inventory of "goods-in-progress".
An alternative water-proofing treatment involves the use of a latex rubber saturant for the paper substrate.
Radiation-curable resins have also been proposed in place of the conventional phenolic resin-modified varnishes as paper substrate saturants. Unfortunately the use of UV-radiation as the cure mechanism can not be applied fromthe backing side. In addition the UV radiation has very limited penetration and if the paper is highly filled, (as is often the case), the grains cast a UV shadow and the cure can be non-uniform. Faster cures may be obtained using electron beam radiation which is much more penetrating. Unfortunately such exposure tends to degrade the paper, leading to a product with reduced internal strength and integrity.
A waterproof paper-backed abrasive product has now been developed which has outstanding water resistance, flexibility and abrasive performance and yet can be produced with a cure time measured in seconds rather than hours or even minutes.
AMEND~D SllE~T
CA 022~07~ 1998-11-16 D-3132 R~P' ~CEME~ AG' General Description of the Invention In a preferred aspect of the invention the paper-backed coated abrasive is provided with a hydrophobic radiation-curable resin maker and/or size coat. The resin is selected to display hydrophobic qualities by which is meant that the cured surface is water-repellant and will not be degraded by water.
This hydrophobicity is caused, or alternatively enhanced, by the addition of a hydrophobic additive w'hich is a siloxane with pendant acrylate functional groups to a binder coat.
The preferred cure mechanism is UV radiation optionally followed, after ~V initiation of the cure,by a thermal treatment. This can often be desirable where full ~V cure is inhibited by the abrasive components or a greater depth of cure is desired.
In the event the radiation cure mechanism employed is electron beam radiation, it is often advisable to provide that the paper used as the backing is reinforced with synthetic fibers that are resistant to degradation when exposed to electron beam radiation. Such papers are frequently referred to as FRP and the use of such papers is a preferred aspect of at least one embodiment of this invention.
Thus the waterproof paper-backed coated abrasive of one embodiment of the invention comprises a cellulosic 30 paper backing reinforced with at least 5% by weight of synthetic polymer fibers resistant to electron beam radiation.
The synthetic polymer fibers are resistant to electron beam radiation and by that is meant that the paper into which they are incorporated at a level of 10%
by weight or more retains at least 25% more of its strength after being submitted to an electron beam A~END~D ~EET
CA 022~07~ l998-ll-l6 W098/03307 PCT~S97/08303 radiation treatment than a cellulosic paper similar in all respects except for the absence of the fiber reinforcement. The fibers in commercial examples of FRP
are often entangled with the cellulosic fibers rather than being laid on the paper surface. In this way, they contribute to or modify the tear strength of the paper.
Such papers are well known commercial products and are used in a wide range of applications.
Detailed Description of the Invention The binder formulation providing one or both of the maker and size coats is one that incorporates a resin that is curable at least in part by radiation, and most preferably by UV radiation. Such resins, which typically polymerize, via a free-radical mechanism, include epoxy-acrylates, aminoplast derivatives having pendant ~
unsaturated carbonyl groups, ethylenically unsaturated compounds, isocyanurate derivatives having at least one pendant acrylate group, isocyanates having at least one pendant acrylate group, urethane-acrylates, epoxy-novolacs and mixtures thereof.
Acrylated urethanes include, for example, diacrylate esters of hydroxyterminated isocyanate extended polyesters or polyethers. Acrylated epoxies include, for example, the diacrylate esters of bisphenol derivatives such bisphenol A epoxy resins. Typical aminoplast derivatives have at least 1.1 pendant ~,~-unsaturated carbonyl groups.
Suitable ethylenically unsaturated compounds include monomeric or polymeric compounds that contain atoms of carbon, hydrogen and oxygen, and optionally nitrogen and the halogens. Oxygen and nitrogen atoms are generally present in ether, ester, urethane, amide or urea groups.
Typical isocyanate derivatives have at least one pendant acrylate group.
CA 022~07~ 1998-11-16 D- 313 2 ~EP'~ MEN~P~.GE
Examples of such resins are conventionally made by the reaction of an acrylate monomer or oligomer, (including di- and tri-acrylates), with a novolac, epoxy or urethane polymer or oligomer. The properties of the final resin can be manipulated by changing the proportions of the components. Usually in the production of a binder resin, the desired properties are hardness and toughness.
The hydrophobic quality of the resin binder is conferred or enhanced by the addition of a copolymerizable siloxane monomer with pendant acrylat'e functionalities that confers hydrophobicity.
Epoxyacrylates often already have a degree of hydrophobicity, particularly those epoxyacrylates that are liquid and require no additional solvents to permit them to be applied in a binder coat. These have the additional advantage that no solvent need be removed during the cure process. One such epoxyacrylate is 20 available from UCB Radcure under the trade name Ebecryl 3 60 5 .
If the binder is cured by UV radiation, a photoinitaitor is usually required to initiate free-radical polymerization. Examples of suitable 25 photoinitiators include, benzophenones, phosphine oxides, nitroso compounds, acryl halides, hydrazones, mercapto compounds, pyrillium compounds, triacrylimidazoles, benzimidazoles, chloroalkyl triazines, benzoin ethers, benzil ketals, thioxanthones, camphorquinone, and 30 acetophenone derivatives. Cationic photoinitiators may also be used and exampes of such photoinitiators include aryl diazonium, arylsulfonium, aryliodonium and ferrocenium salts.
Thermal initiators are often desirable additional 35 components since they can be activated the heat liberated during the cure initiated by the UV cure, thus increasing the degree or depth of cure and possibly eliminating the APJ!ENDED ~ItEET
.
CA 022~07~ 1998-11-16 D- 313 2 REPLACEME~ r RA~E
need for post-cure operations. Suitable thermal intiators include azo compounds, imidazoles and organic peroxides such as diacyl peroxides, acetyl sulfonyl peroxides, dialkyl peroxydicarbonates, tert alkyl peroxyesters, O,O-tert-alkyl )-alkyl monoperoxycarbonates, di(tert-alkylperoxy)ketals, di(tert-alkyl)peroxides, tert-alkyl hydroperoxides and ketone peroxides.
The ~V radiation is usually supplied at a wavelength between about 200 to 700 nanometers and more preferably between about 250 and 400 nanometers. It may be supplemented by a heat treatment applied simultaneously or subsequently to the ~V radiation.
An electron beam radiation treatment, where this is used, typically applies an accelerating voltage of from about 150 kv to 400 kv, though some scanning electron beam devices operate at acceperating voltages in excess of 500 kv. The typical electron beam equipment can penetrate substances with a density of up to about 750 gm/m2 .
The binder formulation derives or enhances its hydrophobicity from the incorporation of a silane or a siloxane having functional groups that enable the silane or siloxane to bond effectively to the binder resin, such as hydroxyl or acrylate functional groups, while retaining an overall hydrophobic character. Silanes are inherently hydrophobic and therefore increase the water resistance of the coated abrasive product. Such a silane is conveniently incorporated in the size coat and additional amounts can also be incorporated in a separate coat applied over the size coat. This can be done in conjunction with other additives such as anti-static or anti-loading additives, or grinding aids. An example of a suitable silane is y-methacryloxypropyltrimethoxy silane and an example of a D'-D ~i~T
, . ~
CA 022~07~ l998-ll-l6 W098/03307 PCT~S97/08303 siloxane that can be used in this function is BYK-371, a siloxane containing pendant acrylate groups available from BYK Chemie.
The abrasive grit bonded to the backing to produce the coated abrasive of the invention can be any of those commonly used to produce coated abrasives. These include aluminum oxide, (both fused and sintered), silicon carbide, fused alumina/zirconia, cubic boron nitride, diamond and blends of any two or more of the above.
Where electron-beam radiation is the selected cure mechanism, as was explained above, it is preferred to use paper incorporating reinforcing fibers, (such reinforced papers are commonly called "FRP"s). Suitable reinforcing fibers for use in preparing the FRPs include polyester, polyolefin, polyamide, polyacrylonitrile, polycarbonate and copolymers of the above as well as mixtures of such fibers.
Commercial FRPs, usually contain about 10~ to about 40~ by weight of the reinforcing polymer fibers. The most preferred reinforcing fibers are made from polyesters such as polyethylene terephthalate or polyamides such as nylon 66. The fibers are usually staple fibers, but it is possible to use tangled continuous filaments also through the FRP production process then becomes somewhat complicated. The diameter of the synthetic polymer fibers is usually about the same as that of the cellulosic fibers with which it is entangled, but the diameter can be somewhat larger or smaller without departing from the essential scope of the invention.
The preferred FRPs used in the products of the invention usually comprise from 10~ to 40~ and preferably from 15~ to 30~ by weight of the synthetic fibers.
Clearly the thicker the fibers, the nearer the top end of this range the synthetic fiber content is likely to be.
, CA 022~07~ 1998-11-16 PEPL~CEMENT ;~AGc' Description of Preferred Embodiments The invention is now described with reference to the following illustrative examples which are not intended to imply any necessary limitation on the essential scope of the present invention.
Drawin~
Figure 1 is a chart showing the hydrophobicity of a formulation according to the invention and the comparison with a formulation lacking the acrlated siloxane derivative.
Example 1 This Example shows the performance of coated abrasive materials made according to the invention with otherwise identical materials made without the hydrophobicity enhancing additives described herein. Coated abrasive materials made in this way were cut into discs for the tests. These were compared using the Schieffer test.
In this test a disc about 11.4cm in diameter is attached to a backup support pad using a ring-clamping device in a horizontal position. An aluminum conduit workpiece made of 6061 aluminum is then moved into contact with the pad at a predetermined constant force and is rotated for a predetermined number of revolutions.
In the present case the force chosen was 8 lbs (35.43 newtons) and the number of revolutions was set at 200.
After this had been completed, the difference in weights of both the workpiece and the disc were measured and recorded.
The test was carried out on discs prepared using discs cut from materials made as follows:
Paper: TPZ0702, an A-weight paper from Kimberly Clark Grain: TGR 1920 (120 grit SiC) or TGR 1910 (180 grit SiC) ~P~r-~,'n,'~
..... .
CA 022~07~ 1998-11-16 - R{PLAC~,E~TP~E
Make Coat: 80/20 blend of Ebecryl 3605/NVP; with 3% Darocure 1173 photoinitiator 1% EMI 24 thermal initiator Size Coat: Blend comprising 24% Ebecryl 3700, 28% ICTA, 28% TMPTA, and 20% TRPGDA, with 3% Darocure 1173 photoinitiator and 4% BYK 371;
or Blend comprising 24% Ebecryl 3700, 28% ICTA, 28% TMPTA, and 20% TRPGDA, with 3% Darocure 1173 photoinitiator.
Ebecryl 3605 is an acrylated epoxy oligomer available under this trade name from UCB Radcure Inc.
NVP is N-vinyl pyrrolidone Darocure 1173 is a photoinitiator from Ciba-Geigy.
EMI-24 is a thermal initiator Ebecryl 3700 is an acrylated epoxy oligomer available under this trade name from UCB Radcure Inc.
ICTA is tris~2-hydroxyethyl)isocyanurate triacrylate TMPTA is tetramethylolpropane triacrylate TRPGDA is tripropyleneglycol diacrylate BYK-371 is a siloxane containing pendant acrylate groups available from BYK Chemie.
Production:
The maker coats were deposited on the same line moving at 10 feet/minute, (3.1 m/mln) and the maker coats were cured using a "D" bulb. Size coating was done on a roll coater and the cure was accomplished using a "D" bulb with the line moving at 50 ft/min., (15.5 m/min.).
The amounts deposited in each case are shown in Table 1.
.~.T' i~r, 't!~D
CA022~07~ 1998-11-16 ~E~LAC~c~T~iE
120 grit 120 grit 180 grit 180 grit Spec. Wt. Actual Wt. Spec. Wt. Actual Wt.
Backing 100.7 100.7 Maker 51.8 (wet) 66.0 37.0 (wet) 47.8 Grain 185.1 199.9 129.6 122.6 Size(Inv)88.8 (wet)72.0 99.9 (wet) 82.9 Size(Comp)88.8 (wet)76.4 99.9 (wet) 78.5 All weights are in terms of g/m2.
The results of the Schieffer testing of the above products were as shown in Table 2 below.
Table 2 SAMPLE CUT LOSS CUT/LOS
(g) (g) S RATIO
Invention 0.315 0.040 7.88 Comparative 0.355 0.060 6.13 Invention 0.300 0.025 12.50 Comparative 0.295 0.035 8.63 To indicate the hydrophobicity of the coated abrasives according to the invention, the water contact angle of a surface coated with the size coat of the comparative example was compared with that of a surface coated with the size coat used in the "invention"
example.
The results are shown in Figure 1 below.
The above results indicate that the addition of the BYK-371 additive clearly improved the cut/loss ration at both grit sizes tested. It was also correlated with a significant increase in hydrophobicity as indicated by the water contact angle.
A~E~JD~D S~IE~
WATERPROOF PAPER-BACKED COATED ABRASIVES
Background to the Invention The present invention relates to the production of coated abrasives and particularly to the production of coated abrasives with a paper backing and more specifically to waterproof coated abrasives.
Such materials typically comprise a paper backing with the grain held by phenolic-modifed varnish resin maker and size coats. The use of the modified varnis'h as the bond renders the product waterproof. However it is found that such products require several hours to complete the cure of the binders and this therefore implies a very large inventory of "goods-in-progress".
An alternative water-proofing treatment involves the use of a latex rubber saturant for the paper substrate.
Radiation-curable resins have also been proposed in place of the conventional phenolic resin-modified varnishes as paper substrate saturants. Unfortunately the use of UV-radiation as the cure mechanism can not be applied fromthe backing side. In addition the UV radiation has very limited penetration and if the paper is highly filled, (as is often the case), the grains cast a UV shadow and the cure can be non-uniform. Faster cures may be obtained using electron beam radiation which is much more penetrating. Unfortunately such exposure tends to degrade the paper, leading to a product with reduced internal strength and integrity.
A waterproof paper-backed abrasive product has now been developed which has outstanding water resistance, flexibility and abrasive performance and yet can be produced with a cure time measured in seconds rather than hours or even minutes.
AMEND~D SllE~T
CA 022~07~ 1998-11-16 D-3132 R~P' ~CEME~ AG' General Description of the Invention In a preferred aspect of the invention the paper-backed coated abrasive is provided with a hydrophobic radiation-curable resin maker and/or size coat. The resin is selected to display hydrophobic qualities by which is meant that the cured surface is water-repellant and will not be degraded by water.
This hydrophobicity is caused, or alternatively enhanced, by the addition of a hydrophobic additive w'hich is a siloxane with pendant acrylate functional groups to a binder coat.
The preferred cure mechanism is UV radiation optionally followed, after ~V initiation of the cure,by a thermal treatment. This can often be desirable where full ~V cure is inhibited by the abrasive components or a greater depth of cure is desired.
In the event the radiation cure mechanism employed is electron beam radiation, it is often advisable to provide that the paper used as the backing is reinforced with synthetic fibers that are resistant to degradation when exposed to electron beam radiation. Such papers are frequently referred to as FRP and the use of such papers is a preferred aspect of at least one embodiment of this invention.
Thus the waterproof paper-backed coated abrasive of one embodiment of the invention comprises a cellulosic 30 paper backing reinforced with at least 5% by weight of synthetic polymer fibers resistant to electron beam radiation.
The synthetic polymer fibers are resistant to electron beam radiation and by that is meant that the paper into which they are incorporated at a level of 10%
by weight or more retains at least 25% more of its strength after being submitted to an electron beam A~END~D ~EET
CA 022~07~ l998-ll-l6 W098/03307 PCT~S97/08303 radiation treatment than a cellulosic paper similar in all respects except for the absence of the fiber reinforcement. The fibers in commercial examples of FRP
are often entangled with the cellulosic fibers rather than being laid on the paper surface. In this way, they contribute to or modify the tear strength of the paper.
Such papers are well known commercial products and are used in a wide range of applications.
Detailed Description of the Invention The binder formulation providing one or both of the maker and size coats is one that incorporates a resin that is curable at least in part by radiation, and most preferably by UV radiation. Such resins, which typically polymerize, via a free-radical mechanism, include epoxy-acrylates, aminoplast derivatives having pendant ~
unsaturated carbonyl groups, ethylenically unsaturated compounds, isocyanurate derivatives having at least one pendant acrylate group, isocyanates having at least one pendant acrylate group, urethane-acrylates, epoxy-novolacs and mixtures thereof.
Acrylated urethanes include, for example, diacrylate esters of hydroxyterminated isocyanate extended polyesters or polyethers. Acrylated epoxies include, for example, the diacrylate esters of bisphenol derivatives such bisphenol A epoxy resins. Typical aminoplast derivatives have at least 1.1 pendant ~,~-unsaturated carbonyl groups.
Suitable ethylenically unsaturated compounds include monomeric or polymeric compounds that contain atoms of carbon, hydrogen and oxygen, and optionally nitrogen and the halogens. Oxygen and nitrogen atoms are generally present in ether, ester, urethane, amide or urea groups.
Typical isocyanate derivatives have at least one pendant acrylate group.
CA 022~07~ 1998-11-16 D- 313 2 ~EP'~ MEN~P~.GE
Examples of such resins are conventionally made by the reaction of an acrylate monomer or oligomer, (including di- and tri-acrylates), with a novolac, epoxy or urethane polymer or oligomer. The properties of the final resin can be manipulated by changing the proportions of the components. Usually in the production of a binder resin, the desired properties are hardness and toughness.
The hydrophobic quality of the resin binder is conferred or enhanced by the addition of a copolymerizable siloxane monomer with pendant acrylat'e functionalities that confers hydrophobicity.
Epoxyacrylates often already have a degree of hydrophobicity, particularly those epoxyacrylates that are liquid and require no additional solvents to permit them to be applied in a binder coat. These have the additional advantage that no solvent need be removed during the cure process. One such epoxyacrylate is 20 available from UCB Radcure under the trade name Ebecryl 3 60 5 .
If the binder is cured by UV radiation, a photoinitaitor is usually required to initiate free-radical polymerization. Examples of suitable 25 photoinitiators include, benzophenones, phosphine oxides, nitroso compounds, acryl halides, hydrazones, mercapto compounds, pyrillium compounds, triacrylimidazoles, benzimidazoles, chloroalkyl triazines, benzoin ethers, benzil ketals, thioxanthones, camphorquinone, and 30 acetophenone derivatives. Cationic photoinitiators may also be used and exampes of such photoinitiators include aryl diazonium, arylsulfonium, aryliodonium and ferrocenium salts.
Thermal initiators are often desirable additional 35 components since they can be activated the heat liberated during the cure initiated by the UV cure, thus increasing the degree or depth of cure and possibly eliminating the APJ!ENDED ~ItEET
.
CA 022~07~ 1998-11-16 D- 313 2 REPLACEME~ r RA~E
need for post-cure operations. Suitable thermal intiators include azo compounds, imidazoles and organic peroxides such as diacyl peroxides, acetyl sulfonyl peroxides, dialkyl peroxydicarbonates, tert alkyl peroxyesters, O,O-tert-alkyl )-alkyl monoperoxycarbonates, di(tert-alkylperoxy)ketals, di(tert-alkyl)peroxides, tert-alkyl hydroperoxides and ketone peroxides.
The ~V radiation is usually supplied at a wavelength between about 200 to 700 nanometers and more preferably between about 250 and 400 nanometers. It may be supplemented by a heat treatment applied simultaneously or subsequently to the ~V radiation.
An electron beam radiation treatment, where this is used, typically applies an accelerating voltage of from about 150 kv to 400 kv, though some scanning electron beam devices operate at acceperating voltages in excess of 500 kv. The typical electron beam equipment can penetrate substances with a density of up to about 750 gm/m2 .
The binder formulation derives or enhances its hydrophobicity from the incorporation of a silane or a siloxane having functional groups that enable the silane or siloxane to bond effectively to the binder resin, such as hydroxyl or acrylate functional groups, while retaining an overall hydrophobic character. Silanes are inherently hydrophobic and therefore increase the water resistance of the coated abrasive product. Such a silane is conveniently incorporated in the size coat and additional amounts can also be incorporated in a separate coat applied over the size coat. This can be done in conjunction with other additives such as anti-static or anti-loading additives, or grinding aids. An example of a suitable silane is y-methacryloxypropyltrimethoxy silane and an example of a D'-D ~i~T
, . ~
CA 022~07~ l998-ll-l6 W098/03307 PCT~S97/08303 siloxane that can be used in this function is BYK-371, a siloxane containing pendant acrylate groups available from BYK Chemie.
The abrasive grit bonded to the backing to produce the coated abrasive of the invention can be any of those commonly used to produce coated abrasives. These include aluminum oxide, (both fused and sintered), silicon carbide, fused alumina/zirconia, cubic boron nitride, diamond and blends of any two or more of the above.
Where electron-beam radiation is the selected cure mechanism, as was explained above, it is preferred to use paper incorporating reinforcing fibers, (such reinforced papers are commonly called "FRP"s). Suitable reinforcing fibers for use in preparing the FRPs include polyester, polyolefin, polyamide, polyacrylonitrile, polycarbonate and copolymers of the above as well as mixtures of such fibers.
Commercial FRPs, usually contain about 10~ to about 40~ by weight of the reinforcing polymer fibers. The most preferred reinforcing fibers are made from polyesters such as polyethylene terephthalate or polyamides such as nylon 66. The fibers are usually staple fibers, but it is possible to use tangled continuous filaments also through the FRP production process then becomes somewhat complicated. The diameter of the synthetic polymer fibers is usually about the same as that of the cellulosic fibers with which it is entangled, but the diameter can be somewhat larger or smaller without departing from the essential scope of the invention.
The preferred FRPs used in the products of the invention usually comprise from 10~ to 40~ and preferably from 15~ to 30~ by weight of the synthetic fibers.
Clearly the thicker the fibers, the nearer the top end of this range the synthetic fiber content is likely to be.
, CA 022~07~ 1998-11-16 PEPL~CEMENT ;~AGc' Description of Preferred Embodiments The invention is now described with reference to the following illustrative examples which are not intended to imply any necessary limitation on the essential scope of the present invention.
Drawin~
Figure 1 is a chart showing the hydrophobicity of a formulation according to the invention and the comparison with a formulation lacking the acrlated siloxane derivative.
Example 1 This Example shows the performance of coated abrasive materials made according to the invention with otherwise identical materials made without the hydrophobicity enhancing additives described herein. Coated abrasive materials made in this way were cut into discs for the tests. These were compared using the Schieffer test.
In this test a disc about 11.4cm in diameter is attached to a backup support pad using a ring-clamping device in a horizontal position. An aluminum conduit workpiece made of 6061 aluminum is then moved into contact with the pad at a predetermined constant force and is rotated for a predetermined number of revolutions.
In the present case the force chosen was 8 lbs (35.43 newtons) and the number of revolutions was set at 200.
After this had been completed, the difference in weights of both the workpiece and the disc were measured and recorded.
The test was carried out on discs prepared using discs cut from materials made as follows:
Paper: TPZ0702, an A-weight paper from Kimberly Clark Grain: TGR 1920 (120 grit SiC) or TGR 1910 (180 grit SiC) ~P~r-~,'n,'~
..... .
CA 022~07~ 1998-11-16 - R{PLAC~,E~TP~E
Make Coat: 80/20 blend of Ebecryl 3605/NVP; with 3% Darocure 1173 photoinitiator 1% EMI 24 thermal initiator Size Coat: Blend comprising 24% Ebecryl 3700, 28% ICTA, 28% TMPTA, and 20% TRPGDA, with 3% Darocure 1173 photoinitiator and 4% BYK 371;
or Blend comprising 24% Ebecryl 3700, 28% ICTA, 28% TMPTA, and 20% TRPGDA, with 3% Darocure 1173 photoinitiator.
Ebecryl 3605 is an acrylated epoxy oligomer available under this trade name from UCB Radcure Inc.
NVP is N-vinyl pyrrolidone Darocure 1173 is a photoinitiator from Ciba-Geigy.
EMI-24 is a thermal initiator Ebecryl 3700 is an acrylated epoxy oligomer available under this trade name from UCB Radcure Inc.
ICTA is tris~2-hydroxyethyl)isocyanurate triacrylate TMPTA is tetramethylolpropane triacrylate TRPGDA is tripropyleneglycol diacrylate BYK-371 is a siloxane containing pendant acrylate groups available from BYK Chemie.
Production:
The maker coats were deposited on the same line moving at 10 feet/minute, (3.1 m/mln) and the maker coats were cured using a "D" bulb. Size coating was done on a roll coater and the cure was accomplished using a "D" bulb with the line moving at 50 ft/min., (15.5 m/min.).
The amounts deposited in each case are shown in Table 1.
.~.T' i~r, 't!~D
CA022~07~ 1998-11-16 ~E~LAC~c~T~iE
120 grit 120 grit 180 grit 180 grit Spec. Wt. Actual Wt. Spec. Wt. Actual Wt.
Backing 100.7 100.7 Maker 51.8 (wet) 66.0 37.0 (wet) 47.8 Grain 185.1 199.9 129.6 122.6 Size(Inv)88.8 (wet)72.0 99.9 (wet) 82.9 Size(Comp)88.8 (wet)76.4 99.9 (wet) 78.5 All weights are in terms of g/m2.
The results of the Schieffer testing of the above products were as shown in Table 2 below.
Table 2 SAMPLE CUT LOSS CUT/LOS
(g) (g) S RATIO
Invention 0.315 0.040 7.88 Comparative 0.355 0.060 6.13 Invention 0.300 0.025 12.50 Comparative 0.295 0.035 8.63 To indicate the hydrophobicity of the coated abrasives according to the invention, the water contact angle of a surface coated with the size coat of the comparative example was compared with that of a surface coated with the size coat used in the "invention"
example.
The results are shown in Figure 1 below.
The above results indicate that the addition of the BYK-371 additive clearly improved the cut/loss ration at both grit sizes tested. It was also correlated with a significant increase in hydrophobicity as indicated by the water contact angle.
A~E~JD~D S~IE~
Claims (10)
1. A paper-backed coated abrasive comprising a hydrophobic radiation-curable resin maker and/or size coat wherein the resin comprises a silane or siloxane with pendant acrylate functional groups.
2. A coated abrasive according to Claim 1 in which the hydrophobic resin is curable by UV radiation.
3 A coated abrasive according to Claim 1 in which the resin is curable using electron beam radiation.
4. A coated abrasive according to Claim 1 in which the resin comprises a liquid epoxyacrylate binder component.
5. A coated abrasive according to Claim 1 in which the paper backing is a fiber reinforced paper.
6. A process for the production of a waterproof paper-backed coated abrasive which comprises applying to a paper backing, in sequence, a maker coat, a layer of abrasive particles and a size coat, wherein at least one of the maker and size coats comprises a hydrophobic resin binder comprising a silane or siloxane with pendant acrylate functional groups and the binder is cured by radiation selected from the group consisting of electron beam radiation and UV radiation.
7. A process according to Claim 6 in which the binder is additionally given a thermal cure treatment.
8. A process according to Claim 6 in which the hydrophobic resin comprises a liquid epoxyacrylate resin.
9. A process according to Claim 6 in which the resin further comprises an additive selected from the group consisting of (meth)acrylate functional silanes and siloxanes and mixtures thereof.
10. A process according to Claim 6 in which a hydrophobic resin is used for both maker and size coats.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/681,236 | 1996-07-22 | ||
| US08/681,236 US5624471A (en) | 1996-07-22 | 1996-07-22 | Waterproof paper-backed coated abrasives |
| PCT/US1997/008303 WO1998003307A1 (en) | 1996-07-22 | 1997-05-19 | Waterproof paper-backed coated abrasives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2255075A1 CA2255075A1 (en) | 1998-01-29 |
| CA2255075C true CA2255075C (en) | 2002-03-26 |
Family
ID=24734394
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002255075A Expired - Fee Related CA2255075C (en) | 1996-07-22 | 1997-05-19 | Waterproof paper-backed coated abrasives |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5624471A (en) |
| EP (1) | EP0921910B1 (en) |
| JP (1) | JPH11513940A (en) |
| KR (1) | KR100341954B1 (en) |
| CN (1) | CN1077830C (en) |
| AT (1) | ATE208245T1 (en) |
| AU (1) | AU706766B2 (en) |
| BR (1) | BR9710748A (en) |
| CA (1) | CA2255075C (en) |
| DE (1) | DE69708122T2 (en) |
| RU (1) | RU2158672C2 (en) |
| TW (1) | TW334488B (en) |
| WO (1) | WO1998003307A1 (en) |
| ZA (1) | ZA974805B (en) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6217432B1 (en) | 1998-05-19 | 2001-04-17 | 3M Innovative Properties Company | Abrasive article comprising a barrier coating |
| US6432549B1 (en) | 1998-08-27 | 2002-08-13 | Kimberly-Clark Worldwide, Inc. | Curl-resistant, antislip abrasive backing and paper |
| US6239049B1 (en) | 1998-12-22 | 2001-05-29 | 3M Innovative Properties Company | Aminoplast resin/thermoplastic polyamide presize coatings for abrasive article backings |
| US6238449B1 (en) | 1998-12-22 | 2001-05-29 | 3M Innovative Properties Company | Abrasive article having an abrasive coating containing a siloxane polymer |
| US6312484B1 (en) | 1998-12-22 | 2001-11-06 | 3M Innovative Properties Company | Nonwoven abrasive articles and method of preparing same |
| US6672952B1 (en) | 1998-12-23 | 2004-01-06 | 3M Innovative Properties Company | Tearable abrasive article |
| US7279438B1 (en) | 1999-02-02 | 2007-10-09 | Certainteed Corporation | Coated insulation board or batt |
| SE516696C2 (en) * | 1999-12-23 | 2002-02-12 | Perstorp Flooring Ab | Process for producing surface elements comprising an upper decorative layer as well as surface elements produced according to the method |
| US7220470B2 (en) * | 2001-02-20 | 2007-05-22 | Certainteed Corporation | Moisture repellent air duct products |
| US7815967B2 (en) * | 2001-09-06 | 2010-10-19 | Alain Yang | Continuous process for duct liner production with air laid process and on-line coating |
| SE525681C2 (en) * | 2001-12-07 | 2005-04-05 | Pergo Ab | Structured panels with matched surface |
| CA2367812A1 (en) * | 2002-01-15 | 2003-07-15 | Robert F. Smith | Abrasive article with hydrophilic/lipophilic coating |
| US20030211262A1 (en) * | 2002-05-08 | 2003-11-13 | Certainteed Corporation | Duct board having two facings |
| US7223455B2 (en) * | 2003-01-14 | 2007-05-29 | Certainteed Corporation | Duct board with water repellant mat |
| US6986367B2 (en) * | 2003-11-20 | 2006-01-17 | Certainteed Corporation | Faced mineral fiber insulation board with integral glass fabric layer |
| SE526728C2 (en) * | 2003-12-11 | 2005-11-01 | Pergo Europ Ab | A method of making panels with a decorative surface |
| US7476427B2 (en) * | 2004-03-11 | 2009-01-13 | Certainteed Corporation | Faced fiberglass board with improved surface toughness |
| US20060019568A1 (en) * | 2004-07-26 | 2006-01-26 | Toas Murray S | Insulation board with air/rain barrier covering and water-repellent covering |
| US20050218655A1 (en) * | 2004-04-02 | 2005-10-06 | Certain Teed Corporation | Duct board with adhesive coated shiplap tab |
| US7435453B2 (en) * | 2004-08-04 | 2008-10-14 | Valspar Sourcing, Inc. | Method of finishing veneer surface of veneered wood product by application and curing of UV-curable coating layers having cationically and free-radically polymerizable moieties |
| US20060057351A1 (en) * | 2004-09-10 | 2006-03-16 | Alain Yang | Method for curing a binder on insulation fibers |
| US20080021415A1 (en) * | 2006-04-07 | 2008-01-24 | Anthony Durkin | Device suitable for connection to a substantially tubular element |
| US20070243804A1 (en) * | 2006-04-14 | 2007-10-18 | Peterson John G | Abrasive article with a resilient dusting surface |
| US20080155904A1 (en) * | 2006-12-31 | 2008-07-03 | 3M Innovative Properties Company | Method of abrading a metal workpiece |
| US20080160879A1 (en) * | 2006-12-31 | 2008-07-03 | 3M Innovative Properties Company | Method of abrading a zirconium-based alloy workpiece |
| FR2924041B1 (en) * | 2007-11-26 | 2010-04-30 | Arjowiggins Licensing Sas | PROCESS FOR PRODUCING A REINFORCED APPLIED ABRASIVE PRODUCT AND PRODUCT OBTAINED |
| CN102639665B (en) * | 2009-12-03 | 2015-04-01 | 3M创新有限公司 | Method of electrostatic deposition of particles, abrasive grain and articles |
| MX366743B (en) * | 2012-04-13 | 2019-07-04 | Sigma Alimentos Sa De Cv | Hydrophobic paper or cardboard with self-assembled nanoparticles and method for the production thereof. |
| CN102941538B (en) * | 2012-11-12 | 2015-02-18 | 江苏锋芒复合材料科技集团有限公司 | Water-based environmental-friendly paper base class coated abrasive tool and method for detecting adhesive property of same |
| US20200266161A1 (en) * | 2019-02-15 | 2020-08-20 | Mikro Mesa Technology Co., Ltd. | Detachable bonding structure and method of forming thereof |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4047903A (en) * | 1972-09-26 | 1977-09-13 | Hoechst Aktiengesellschaft | Process for the production of abrasives |
| JPS5265391A (en) * | 1975-11-26 | 1977-05-30 | Kansai Paint Co Ltd | Method of manufactring grinding sheets |
| SU686864A1 (en) * | 1977-05-12 | 1979-09-25 | Научно-Исследовательский И Технологический Институт Абразивной Промышленности | Method of manufacturing of grinding cloth base |
| CS199139B1 (en) * | 1978-05-19 | 1980-07-31 | Jiri Krystufek | Method of pretreating textile substrates for emery sheets |
| US4457766A (en) * | 1980-10-08 | 1984-07-03 | Kennecott Corporation | Resin systems for high energy electron curable resin coated webs |
| JPS58220893A (en) * | 1982-06-18 | 1983-12-22 | 大日精化工業株式会社 | Prevention of curl of paper |
| JPS6279243A (en) * | 1985-10-01 | 1987-04-11 | Nippon Shokubai Kagaku Kogyo Co Ltd | Active energy beam curable composition |
| DE3852661D1 (en) * | 1987-03-27 | 1995-02-16 | Ciba Geigy Ag | Photo-curable abrasives. |
| JPH05202153A (en) * | 1992-01-28 | 1993-08-10 | Shin Etsu Polymer Co Ltd | Ultraviolet ray-curable resin composition |
| DE69530976D1 (en) * | 1994-03-16 | 2003-07-10 | Minnesota Mining & Mfg | ABRASIVE OBJECTS AND METHOD FOR THEIR PRODUCTION |
-
1996
- 1996-07-22 US US08/681,236 patent/US5624471A/en not_active Expired - Lifetime
-
1997
- 1997-05-19 BR BR9710748A patent/BR9710748A/en not_active IP Right Cessation
- 1997-05-19 DE DE69708122T patent/DE69708122T2/en not_active Revoked
- 1997-05-19 KR KR1019997000430A patent/KR100341954B1/en not_active IP Right Cessation
- 1997-05-19 WO PCT/US1997/008303 patent/WO1998003307A1/en active IP Right Grant
- 1997-05-19 CN CN97195101A patent/CN1077830C/en not_active Expired - Fee Related
- 1997-05-19 RU RU98123116/02A patent/RU2158672C2/en not_active IP Right Cessation
- 1997-05-19 AT AT97925596T patent/ATE208245T1/en not_active IP Right Cessation
- 1997-05-19 JP JP10506904A patent/JPH11513940A/en active Pending
- 1997-05-19 AU AU30686/97A patent/AU706766B2/en not_active Ceased
- 1997-05-19 CA CA002255075A patent/CA2255075C/en not_active Expired - Fee Related
- 1997-05-19 EP EP97925596A patent/EP0921910B1/en not_active Revoked
- 1997-05-30 ZA ZA9704805A patent/ZA974805B/en unknown
- 1997-06-12 TW TW086108139A patent/TW334488B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU706766B2 (en) | 1999-06-24 |
| ATE208245T1 (en) | 2001-11-15 |
| DE69708122T2 (en) | 2002-08-01 |
| CN1220628A (en) | 1999-06-23 |
| TW334488B (en) | 1998-06-21 |
| RU2158672C2 (en) | 2000-11-10 |
| DE69708122D1 (en) | 2001-12-13 |
| WO1998003307A1 (en) | 1998-01-29 |
| ZA974805B (en) | 1997-12-30 |
| AU3068697A (en) | 1998-02-10 |
| EP0921910B1 (en) | 2001-11-07 |
| KR20000067945A (en) | 2000-11-25 |
| JPH11513940A (en) | 1999-11-30 |
| US5624471A (en) | 1997-04-29 |
| CA2255075A1 (en) | 1998-01-29 |
| CN1077830C (en) | 2002-01-16 |
| BR9710748A (en) | 1999-08-17 |
| KR100341954B1 (en) | 2002-06-26 |
| EP0921910A1 (en) | 1999-06-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20130521 |