EP0227394A2 - Coated abrasive suitable for use as a lapping material - Google Patents
Coated abrasive suitable for use as a lapping material Download PDFInfo
- Publication number
- EP0227394A2 EP0227394A2 EP86309714A EP86309714A EP0227394A2 EP 0227394 A2 EP0227394 A2 EP 0227394A2 EP 86309714 A EP86309714 A EP 86309714A EP 86309714 A EP86309714 A EP 86309714A EP 0227394 A2 EP0227394 A2 EP 0227394A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- abrasive
- composition
- lapping
- backing
- binder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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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
- B24D3/001—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 supporting member
-
- 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
Definitions
- This invention relates to novel coated abrasives, and, in particular, to a lapping material in sheet form.
- “Lapping”, as the term is used in this specification, means working a particulate abrasive material against the surface of a workpiece until an exceedingly fine, mirror-like finish is imparted thereto.
- the objective sought is the attainment of a very smooth surface finish, while retaining a high degree of dimensional control, so that the resulting product will conform to very precise size standards.
- the lapping of surfaces from their original state to the final finish is a progressive operation, involving the use of a series of abrasives ranging from relatively coarse at the beginning through successively finer sizes to the end.
- results secured depend upon a number of factors, such as the properties of the abrasive employed, the pressure with which the abrasive is forced against the workpiece, the pattern of movement preserved in the contact of the workpiece with the abrasive particles and other considerations.
- U.S. Patent 4,288,233 describes lapping pads for ophthalmic lenses. While the lapping material of this invention is useful, the components thereof, i.e. diamonds, and the method of making it, i.e. metal plating, are expensive. Furthermore the lapping0227394 materials described therein are not flexible.
- U.S. Patent 4,255,164 discloses a glass fining sheet suited for finishing rough ground vitreous surfaces to provide a surface finish which may be readily polished comprising a flexible, conformable backing sheet bearing a microcellular abrasive granule-resin matrix which, under use conditions and in the presence of an aqueous flow, generates a fining slurry.
- the fining sheet is prepared by coating a flexible conformable backing sheet with a foamed liquid abrasive granule-resin coating composition comprised of liquid curable binder material, abrasive fining granules, and sufficient compatible solvent to provide a coatable composition.
- the coating provides a cellular layer which releases the fining abrasive granules at a controlled rate under use conditions.
- the released granules perform the actual abrading.
- the sheet of this patent appears to be another means of preparing a fining slurry.
- the invention involves a method of preparing a coated abrasive which is especially useful as a lapping material.
- the method comprises the steps of:
- the curable binder is preferably curable by radiation, and it may also be curable by thermal energy.
- the abrasive grains are of a size typically used for lapping; i.e., they can have an average particle size of up to about 35 micrometers.
- the backing is preferably primed to promote adhesion between it and the cured binder.
- the coatable composition does not require a solvent, although a solvent may be used, if desired, for some purposes.
- the method of this invention is low in cost due to the savings derived from eliminating the solvent and solvent removal steps.
- this invention involves a coated abrasive suitable for use as a lapping material comprising a backing, lapping size abrasive grains, and a binder which adheres said grains to the backing.
- the coated abrasive of this invention exhibits high endurance for extended periods of use.
- the coated abrasive can be die cut to shape, if desired, e.g., for specialty microfinishing apparatus.
- curable binder means the flowable or coatable composition from which the binder is prepared by means by free-radical polymerization;
- binder or “cured binder” means the dry, polymerized coating which adheres the abrasive grains to the backing.
- the backing should be sufficiently strong to support the binder and abrasive grains therein under contemplated use conditions. It should be sufficiently flexible to allow mounting thereof on the surfaces of lapping tools. Because most lapping operations require the use of water or oil or both, it is preferred that the backing be water-resistant and oil-resistant. it is also preferred that the backing be smooth and of uniform caliper so the lapping film can be used successfully for finishing high precision articles.
- Materials suitable for the backing include water-resistant paper and polymeric films. If polymeric film is to be used as a backing, it should preferably have a primed surface to promote adhesion between the backing and the binder.
- the preferred primer for the purposes of this invention is ethylene acrylic acid as described in U.S. Patent 3,188,265, incorporated herein by reference. Alternatively polymeric film having a roughened surface can provide excellent adhesion between the backing and binder.
- the preferred backing material is polyester, e.g. polyethylene terephthalate, which has been oriented and heat set and primed with ethylene acrylic
- the backing should be sufficiently thick to provide sufficient strength to bear the coating, but not so thick as to adversely affect flexibility.
- the backing should have a thickness of less than about 10 mils, and a thickness of 2 to 3 mils is preferred.
- the abrasive grains can be any abrasive grain conventionally used for lapping processes.
- Abrasives suitable for the lapping film of this invention include iron oxide, silicon carbide, silicon nitride, silicon boride, diamond, aluminum oxide, chromic oxide, and alumina and magnesia spinel ceramic prepared in accordance with U.S. Patent 4,314,827, referred to by the trademark Cubitron(l), commercially available from Minnesota Mining and Manufacturing Company, St. Paul, MN.
- the size range of the grains can range from about 0.2 to about 35 micrometers, the preferred range being from about 1 to about 20 micrometers. It is preferred that for a given lapping film, the grain size range be as narrow as possible, because a small number of excessively large grains can result in scratches on the workpiece surface. An excessive number of fine grains, however, will not result in this problem.
- the curable binder is curable by free-radical polymerization, preferably by radiation-initiation or generation of free-radicals.
- Sources of radiation that are useful for the process of the present invention include ultraviolet, visible, y-radiation, X-rays, and electron beam, with electron beam being most preferred.
- the curable binder can also be cured by thermal energy in the presence of an appropriate catalyst.
- Suitable curable binders for use in this invention comprise radiation-curable monomers, and, optionally, reactive diluents.
- the curable binder may also contain conventional additives, for example, wetting agents, lubricants, dispersing agents, fillers, and coupling agents.
- Radiation-curable monomers that are useful in this invention contain at least two ethylenically unsaturated moieties therein, e.g. acrylic (such as hexane diol diacrylate), methacrylic (such as hexane diol dimethacrylate).
- acrylic such as hexane diol diacrylate
- methacrylic such as hexane diol dimethacrylate
- Radiation-curable monomers that are preferred include oligomers selected from urethane acrylates and methacrylates, isocyanurate acrylates and methacrylates, polyester-urethane acrylates and methacrylates, and epoxy acrylates and methacrylates.
- One class of oligomers that are preferred for the compositions for preparing the binders can be represented by the general formula: where
- ZOH represents an aliphatic group having at least one acrylate functional group therein.
- Z can be represented by the structural formula wherein R', R" and x are as defined above.
- DBTDL represents dibutyl tin dilaurate, a catalyst
- the cyclic trimer of hexamethylene diisocyanate is commercially available from Mobay Chemical Corp. and 2,2,4-trimethylhexamethylene isocyanate is commercially available from Thorson Chemical.
- a coupling agent be included with the monomer in order to promote adhesion between the abrasive grains and the cured binder. Improved adhesion between cured binder and abrasive grains inhibits the grains from being loosened and removed from the binder during lapping operations, thus enhancing the durability of the lapping film.
- a preferred coupling agent is -methacryloxypropyl trimethoxy silane commercially available from Dow Corning Corp. under the trade designation Z6030 and Union Carbide Corp. under the trade designation A-174.
- the amount of coupling agent ranges from about 0.1 to about 10% by weight, preferably from about 1.5 to about 5% by weight, based on weight of abrasive grains.
- Reactive diluents suitable for the present invention include mono- or multifunctional acrylates and methacrylates such as hexane diol diacrylate (HDDA), pentaerythritol triacrylate (PET 3 A), pentaerythritol tetraacrylate (PET 4 A), trimethylolpropanetriacrylate (TMPTA), -hydroxyethylmethacrylate (HEMA), tetrahydrofuran acrylate (THF-A) the preferred specie.
- HDDA hexane diol diacrylate
- PET 3 A pentaerythritol triacrylate
- PET 4 A pentaerythritol tetraacrylate
- TMPTA trimethylolpropanetriacrylate
- HEMA -hydroxyethylmethacrylate
- THF-A tetrahydrofuran acrylate
- the reactive diluent serves to reduce the viscosity of the composition for preparing the binder, thus improving the coatability of the composition, and to modify the hardness of the cured binder.
- the ratio of monomer to reactive diluent is 85:15 to 25:75, more preferably, the ratio is 75:25 to 35:65, and most preferably, the ratio is 65:35 to 45:55.
- the cured binder can have a Knoop hardness, as measured on a Tukon® indentation tester, from about 1 to about 50.
- the Knoop hardness preferably ranges from about 7 to about 25.
- the cured binder should be compatible with the backing and primer thereon, i.e. the binder should be free of fisheyes, craters, voids, and orange-peels when coated and cured.
- the coated abrasive of this invention can vary with respect to product requirements. Depending upon the function of the coated abrasive, the user can specify hardness of cured binder and size of abrasive grains. For example, ophthalmic pads are characterized by a very hard resin combined with a relatively coarse mineral. Disc burnishing films are characterized by softer resin and finer mineral.
- the coated abrasive of this invention can be prepared by applying the curable binder and abrasive grains suspended therein onto the backing to form a coating and then curing the thus-applied coating by free-radical polymerization.
- the following method has been found to be useful in preparing the coated abrasive.
- the dry mineral grains first be treated with coupling agent. After the mineral grains are treated with coupling agent, they are then heat set in an oven. Typically, heat setting is conducted at 60°C-100°C for 1-1/2 to 2-1/2 hours.
- the coupling agent can be mixed in the curable binder along with the dry mineral grains.
- the grains of abrasive mineral are added to the curable binder under conditions of high-shear mixing.
- the composition is then applied, preferably by means of conventional coating equipment, to the backing.
- the viscosity of the composition determines the ease of coating.
- the viscosity of the composition can range from about 200 to about 5,000,000 centipoise at 25°C, preferably about 2000 to about 500,000. At higher temperatures, more viscous compositions can be used. For example, a composition having a viscosity of 30,000 centipoise at 25°C can be coated fairly easily at 50°C.
- Rotogravure coating is preferred for the reason that the rotogravure coater can impart a uniform pattern of ridges and valleys to the binder composition, which, after the composition is cured, can serve as channels for flow of lubricants and for removal of abraded material.
- the coating is then cured by means of free-radical polymerization.
- the free-radical polymerization is initiated by actinic radiation, preferably electron beam.
- actinic radiation preferably electron beam.
- other sources of radiation such as ultraviolet, visible, and gamma, are also suitable with appropriate catalyst.
- Thermal initiation is also suitable with an appropriate catalyst.
- solvents are not required to be added to the curable binder to facilitate coating thereof onto the backing. This has the advantage of avoiding troublesome solvent removal problems.
- an inert solvent can be employed along with the monomers, reactive diluents, and coupling agent of the curable binder.
- ophthalmic pads were prepared and tested.
- the testing procedures were designated as (a) first fine, (b) second fine, and (c) single fine. These testing procedures are designed to measure the amount of material removed and the character of finish imparted to a plastic CR-39 lens.
- First fine samples were prepared and tested according to the following procedure:
- the backside of the material to be tested was laminated with a pressure-sensitive adhesive.
- An ophthalmic test daisy was die cut with a standard die. The test daisy was mounted on a 2.12 diopter spherical lapping block. The lapping block was mounted on a Coburn Rocket lapping machine. The initial thickness of the lens was measured, and then the lens was clamped over the lapping block, air pressure was set at 20 psi. The lens and lapping blocks were flooded with water. A one minute test was run at settings of "medium” and "20 mm top stroke". The lens was removed and final thickness measured. Finish was measured with a Surtronic 3 instrument.
- Second fine samples were prepared and tested according to the same procedure, the only difference being that the test was run for two minutes, instead of one minute, and a 6.25/8.25 diopter lapping block was used.
- the contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, that the reaction temperature is maintained at about 70°C.
- 2.3 equivalents of pentaerythritoltriacrylate (“Sartomer”) was added to the reaction vessel over a 15 minute period. Heat was applied to maintain a reaction temperature of 70-80°C until the reaction was complete as determined by % NCO.
- the contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, that the reaction temperature was maintained at about 70°C.
- 5.0 equivalents of pentaerythritoltriacrylate (“Sartomer") was added to the reaction vessel over a 15 minute period. Heat was applied to maintain a reaction temperature of 70-80°C until the reaction was complete as determined by % NCO.
- the coated abrasive of the present invention exhibited improved results according to the second fine test procedure, as the cut was dramatically increased while finish and abrasive wear continued to be acceptable.
- This example demonstrates the preferred combination of monomer, reactive diluent, coupling agent, and abrasive grain.
- the monomers, and reactive diluents were blended, and abrasive grains pretreated with gamma-methacryloxypropyltrimethoxysilane coupling agent (Z6030) was introduced into the mixture.
- Dyes were also utilized in the mixtures so that the size of the abrasive grains in each run could be identified.
- the ratios of ingredients are set forth in Table III.
- compositions were knife coated at 1 mil thickness on ethylene acrylic acid primed polyethylene terephthalate film.
- the coated film was subjected to electron beam radiation at 250 Kev, 8 Mrad.
Abstract
- (a) providing a coatable composition comprising a binder curable by free-radical polymerization, said composition having lapping size abrasive grains suspended therein,
- (b) coating said composition on a backing, and
- (c) curing said composition by means of free-radical polymerization.
Description
- This invention relates to novel coated abrasives, and, in particular, to a lapping material in sheet form.
- "Lapping", as the term is used in this specification, means working a particulate abrasive material against the surface of a workpiece until an exceedingly fine, mirror-like finish is imparted thereto. The objective sought is the attainment of a very smooth surface finish, while retaining a high degree of dimensional control, so that the resulting product will conform to very precise size standards. The lapping of surfaces from their original state to the final finish is a progressive operation, involving the use of a series of abrasives ranging from relatively coarse at the beginning through successively finer sizes to the end. The results secured depend upon a number of factors, such as the properties of the abrasive employed, the pressure with which the abrasive is forced against the workpiece, the pattern of movement preserved in the contact of the workpiece with the abrasive particles and other considerations.
- The earliest methods of lapping employed particulate abrasive materials suspended in a liquid vehicle to form a slurry. The suspension was worked against the surface of the workpiece until the desired finish was attained. Examples of lapping methods employing abrasive slurries are described in U.S. Patents 2,655,775; 4,059,929; 4,046,524; 4,246,003.
- More recently, lapping materials in pad or sheet form have been developed. U.S. Patent 4,288,233 describes lapping pads for ophthalmic lenses. While the lapping material of this invention is useful, the components thereof, i.e. diamonds, and the method of making it, i.e. metal plating, are expensive. Furthermore the lapping0227394 materials described therein are not flexible.
- U.S. Patent 4,255,164 discloses a glass fining sheet suited for finishing rough ground vitreous surfaces to provide a surface finish which may be readily polished comprising a flexible, conformable backing sheet bearing a microcellular abrasive granule-resin matrix which, under use conditions and in the presence of an aqueous flow, generates a fining slurry. The fining sheet is prepared by coating a flexible conformable backing sheet with a foamed liquid abrasive granule-resin coating composition comprised of liquid curable binder material, abrasive fining granules, and sufficient compatible solvent to provide a coatable composition. The coating provides a cellular layer which releases the fining abrasive granules at a controlled rate under use conditions. The released granules perform the actual abrading. The sheet of this patent appears to be another means of preparing a fining slurry.
- In one aspect, the invention involves a method of preparing a coated abrasive which is especially useful as a lapping material. The method comprises the steps of:
- (a) providing a coatable composition comprising a binder curable by free radical polymerization having lapping size abrasive grains suspended therein,
- (b) applying said coatable composition to a backing, and
- (c) curing said composition by means of free radical polymerization.
- The curable binder is preferably curable by radiation, and it may also be curable by thermal energy. The abrasive grains are of a size typically used for lapping; i.e., they can have an average particle size of up to about 35 micrometers. The backing is preferably primed to promote adhesion between it and the cured binder. The coatable composition does not require a solvent, although a solvent may be used, if desired, for some purposes.
- The method of this invention is low in cost due to the savings derived from eliminating the solvent and solvent removal steps.
- In another aspect, this invention involves a coated abrasive suitable for use as a lapping material comprising a backing, lapping size abrasive grains, and a binder which adheres said grains to the backing.
- The coated abrasive of this invention exhibits high endurance for extended periods of use. The coated abrasive can be die cut to shape, if desired, e.g., for specialty microfinishing apparatus.
- As used herein, the term "curable binder" means the flowable or coatable composition from which the binder is prepared by means by free-radical polymerization; the term "binder" or "cured binder" means the dry, polymerized coating which adheres the abrasive grains to the backing.
- The backing should be sufficiently strong to support the binder and abrasive grains therein under contemplated use conditions. It should be sufficiently flexible to allow mounting thereof on the surfaces of lapping tools. Because most lapping operations require the use of water or oil or both, it is preferred that the backing be water-resistant and oil-resistant. it is also preferred that the backing be smooth and of uniform caliper so the lapping film can be used successfully for finishing high precision articles. Materials suitable for the backing include water-resistant paper and polymeric films. If polymeric film is to be used as a backing, it should preferably have a primed surface to promote adhesion between the backing and the binder. The preferred primer for the purposes of this invention is ethylene acrylic acid as described in U.S. Patent 3,188,265, incorporated herein by reference. Alternatively polymeric film having a roughened surface can provide excellent adhesion between the backing and binder. The preferred backing material is polyester, e.g. polyethylene terephthalate, which has been oriented and heat set and primed with ethylene acrylic acid.
- The backing should be sufficiently thick to provide sufficient strength to bear the coating, but not so thick as to adversely affect flexibility. Typically, the backing should have a thickness of less than about 10 mils, and a thickness of 2 to 3 mils is preferred.
- The abrasive grains can be any abrasive grain conventionally used for lapping processes. Abrasives suitable for the lapping film of this invention include iron oxide, silicon carbide, silicon nitride, silicon boride, diamond, aluminum oxide, chromic oxide, and alumina and magnesia spinel ceramic prepared in accordance with U.S. Patent 4,314,827, referred to by the trademark Cubitron(l), commercially available from Minnesota Mining and Manufacturing Company, St. Paul, MN. The size range of the grains can range from about 0.2 to about 35 micrometers, the preferred range being from about 1 to about 20 micrometers. It is preferred that for a given lapping film, the grain size range be as narrow as possible, because a small number of excessively large grains can result in scratches on the workpiece surface. An excessive number of fine grains, however, will not result in this problem.
- The curable binder is curable by free-radical polymerization, preferably by radiation-initiation or generation of free-radicals. Sources of radiation that are useful for the process of the present invention include ultraviolet, visible, y-radiation, X-rays, and electron beam, with electron beam being most preferred. The curable binder can also be cured by thermal energy in the presence of an appropriate catalyst.
- Suitable curable binders for use in this invention comprise radiation-curable monomers, and, optionally, reactive diluents. The curable binder may also contain conventional additives, for example, wetting agents, lubricants, dispersing agents, fillers, and coupling agents.
- Radiation-curable monomers that are useful in this invention contain at least two ethylenically unsaturated moieties therein, e.g. acrylic (such as hexane diol diacrylate), methacrylic (such as hexane diol dimethacrylate).
- Radiation-curable monomers that are preferred include oligomers selected from urethane acrylates and methacrylates, isocyanurate acrylates and methacrylates, polyester-urethane acrylates and methacrylates, and epoxy acrylates and methacrylates.
-
- n represents 2 or 3,
- x represents 1 to 3 inclusive,
- R represents an aliphatic group having, for example, from 1 to 20 carbon atoms, a cycloaliphatic group having, for example, from 5 to 6 ring carbon atoms, and up to 36 carbon atoms in total, or an aromatic group, for example benzyl,
- R' represents an aliphatic group having, for example, from 2 to 10 carbon atoms,
- R" represents hydrogen or a methyl group.
-
-
- The cyclic trimer of hexamethylene diisocyanate is commercially available from Mobay Chemical Corp. and 2,2,4-trimethylhexamethylene isocyanate is commercially available from Thorson Chemical. Representative examples of commercially available starting materials that can be characterized by the formula ZOH, supra, include pentaerythritoltriacrylate (available from Sartomer), hydroxyethyl methacrylate (available from Rohm and Haas Co.), and hydroxyethyl acrylate (available from Dow Chemical Co.).
- It is preferred that a coupling agent be included with the monomer in order to promote adhesion between the abrasive grains and the cured binder. Improved adhesion between cured binder and abrasive grains inhibits the grains from being loosened and removed from the binder during lapping operations, thus enhancing the durability of the lapping film. A preferred coupling agent is -methacryloxypropyl trimethoxy silane commercially available from Dow Corning Corp. under the trade designation Z6030 and Union Carbide Corp. under the trade designation A-174. Preferably, the amount of coupling agent ranges from about 0.1 to about 10% by weight, preferably from about 1.5 to about 5% by weight, based on weight of abrasive grains.
- It is also preferred to include a reactive diluent with the monomer. Reactive diluents suitable for the present invention include mono- or multifunctional acrylates and methacrylates such as hexane diol diacrylate (HDDA), pentaerythritol triacrylate (PET3A), pentaerythritol tetraacrylate (PET4A), trimethylolpropanetriacrylate (TMPTA), -hydroxyethylmethacrylate (HEMA), tetrahydrofuran acrylate (THF-A) the preferred specie. The reactive diluent serves to reduce the viscosity of the composition for preparing the binder, thus improving the coatability of the composition, and to modify the hardness of the cured binder. Preferably, the ratio of monomer to reactive diluent is 85:15 to 25:75, more preferably, the ratio is 75:25 to 35:65, and most preferably, the ratio is 65:35 to 45:55.
- The cured binder can have a Knoop hardness, as measured on a Tukon® indentation tester, from about 1 to about 50. The Knoop hardness preferably ranges from about 7 to about 25.
- The cured binder should be compatible with the backing and primer thereon, i.e. the binder should be free of fisheyes, craters, voids, and orange-peels when coated and cured.
- The coated abrasive of this invention can vary with respect to product requirements. Depending upon the function of the coated abrasive, the user can specify hardness of cured binder and size of abrasive grains. For example, ophthalmic pads are characterized by a very hard resin combined with a relatively coarse mineral. Disc burnishing films are characterized by softer resin and finer mineral.
- The coated abrasive of this invention can be prepared by applying the curable binder and abrasive grains suspended therein onto the backing to form a coating and then curing the thus-applied coating by free-radical polymerization. The following method has been found to be useful in preparing the coated abrasive.
- It is preferred that the dry mineral grains first be treated with coupling agent. After the mineral grains are treated with coupling agent, they are then heat set in an oven. Typically, heat setting is conducted at 60°C-100°C for 1-1/2 to 2-1/2 hours. Alternatively, the coupling agent can be mixed in the curable binder along with the dry mineral grains.
- After the monomers and the reactive diluents, if any, are blended to form the curable binder, the grains of abrasive mineral are added to the curable binder under conditions of high-shear mixing. The composition is then applied, preferably by means of conventional coating equipment, to the backing. The viscosity of the composition determines the ease of coating. The viscosity of the composition can range from about 200 to about 5,000,000 centipoise at 25°C, preferably about 2000 to about 500,000. At higher temperatures, more viscous compositions can be used. For example, a composition having a viscosity of 30,000 centipoise at 25°C can be coated fairly easily at 50°C. Rotogravure coating is preferred for the reason that the rotogravure coater can impart a uniform pattern of ridges and valleys to the binder composition, which, after the composition is cured, can serve as channels for flow of lubricants and for removal of abraded material. The coating is then cured by means of free-radical polymerization. Preferably, the free-radical polymerization is initiated by actinic radiation, preferably electron beam. However, other sources of radiation, such as ultraviolet, visible, and gamma, are also suitable with appropriate catalyst. Thermal initiation is also suitable with an appropriate catalyst.
- It should be noted that solvents are not required to be added to the curable binder to facilitate coating thereof onto the backing. This has the advantage of avoiding troublesome solvent removal problems. If desired, an inert solvent can be employed along with the monomers, reactive diluents, and coupling agent of the curable binder.
- In order to demonstrate the performance characteristics of the coated abrasive of the present invention, ophthalmic pads were prepared and tested. The testing procedures were designated as (a) first fine, (b) second fine, and (c) single fine. These testing procedures are designed to measure the amount of material removed and the character of finish imparted to a plastic CR-39 lens. First fine samples were prepared and tested according to the following procedure:
- The backside of the material to be tested was laminated with a pressure-sensitive adhesive. An ophthalmic test daisy was die cut with a standard die. The test daisy was mounted on a 2.12 diopter spherical lapping block. The lapping block was mounted on a Coburn Rocket lapping machine. The initial thickness of the lens was measured, and then the lens was clamped over the lapping block, air pressure was set at 20 psi. The lens and lapping blocks were flooded with water. A one minute test was run at settings of "medium" and "20 mm top stroke". The lens was removed and final thickness measured. Finish was measured with a Surtronic 3 instrument.
- Second fine samples were prepared and tested according to the same procedure, the only difference being that the test was run for two minutes, instead of one minute, and a 6.25/8.25 diopter lapping block was used.
- Single fine were prepared and tested according to same procedure as the first fine, the only difference being that the test was run for three minutes, instead of one minute.
- In the examples which follow, the following abbreviations will be used:
- HMDIT-A5:
- TMDI-A4:
- TMDI-A6:
- n-BUMA: n-butyl(2-methacryloxy) ethyl carbamate
- THF-A: tetrahydrofurfuryl acrylate
- HDDA: hexane diol diacrylate
- TMPTA: trimethylolpropanetriacrylate
- PET3A: pentaerythritol triacrylate
- PET4A: pentaerythritol tetraacrylate
- To one-gallon reaction vessel equipped with a thermometer, mechanical stirrpr, and a dry air sparge was charged 6.5 equivalent of the trimer of hexamethylene diisocyanate ("Desmondur-N-3390"). In a second vessel, 2.5 g tetra-cis-methylene-3,3,5-di-t-butyl-4-hydroxyphenyl- propionatemethane ("Irganox 1010") was dissolved with heat and stirring into 4.6 equivalent of hydroxyethylmethacrylate (HEMA). Dibutyltindilaurate (8 to 10 drops) was then charged to the vessel containing HEMA. The contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, that the reaction temperature is maintained at about 70°C. At the end of the 30-minute period, 2.3 equivalents of pentaerythritoltriacrylate ("Sartomer") was added to the reaction vessel over a 15 minute period. Heat was applied to maintain a reaction temperature of 70-80°C until the reaction was complete as determined by % NCO.
- To a one gallon reaction vessel'equipped with a thermometer, mechanical stirrer, and a dry air sparge was charge 10 equivalents of 2,2,4-trimethylhexamethylene- diisocyanate. In a second vessel, 3.0 g of tetra-cis- methylene-3,3,5-di-t-butyl-4-hydroxyphenylpropionatemethane ,("Irganox 1010") was dissolved with heat and stirring into 5.35 equivalents of hydroxyethylmethacrylate (HEMA). Dibutyltindilaurate (8 to 10 drops) was then charged to the vessel containing HEMA. The contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, that the reaction temperature was maintained at about 70°C. At the end of the 30-minute period, 5.0 equivalents of pentaerythritoltriacrylate ("Sartomer") was added to the reaction vessel over a 15 minute period. Heat was applied to maintain a reaction temperature of 70-80°C until the reaction was complete as determined by % NCO.
- To a one gallon reaction vessel equipped with a thermometer, mechanical stirrer, and a dry air sparge was charged 7.0 equivalents of 2,2,4-trimethylhexamethylene diisocyanate. In a second vessel, 3.0g of tetra-cis- methylene-3,3,5-di-t-butyl-4-hydroxyphenylpropionatemethane ("Irganox 1010") was dissolved with heat and stirring, into 7.3 equivalents of.pentaerythritoltriacrylate ("Sartomer"). Dibutyltindilaurate (8 to 10 drops) was then charged to the vessel containing the PET3A. The contents of the second vessel were charged to the first over a 30 min. period, with heating and cooling, to maintain a temperature of 70°C. The reaction mixture was heated to maintain a temperature of 70-80°C until the raction is complete by % NCO.
- To a one gallon reaction vessel equipped with a thermometer, mechanical stirrer, and a dry air sparge was charged 10 equivalents of n-butylisocyanate. In a second vessel, 2.5 g tetra-cis-methylene-3,3,5-di-t-butyl-4-hydroxyphenylpropionatemethane ("Irganox 1010") was dissolved with heat and stirring into 11 equivalents of hydroxyethylmethacrylate (HEMA). Dibutyltindilaurate (8 to 10 drops) was then charged to the vessel containing HEMA. The contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, that the reaction temperature was maintained at about 70°C until the reaction was complete as determined by % NCO.
- To a one gallon reaction vessel equipped with a thermometer, mechanical stirrer, and a dry air sparge was charged 5.0 equivalents of the trimer of hexamethylenediisocyanate ("Desmondur-N-3390"). In a second vessel, 3.0 g tetra-cis-methylene-3,35-di-t-butyl-4-hydroxyphenyl- propionatemethane ("Irganox 1010") was dissolved with heat and stirring into 5.25 equivalents of pentaerythritoltriacrylate (PET3A). Dibutyltindilaurate (8 to 10 drops) was then charged to the vessel containing PET3A. The contents of the second vessel were charged to the reaction vessel over a 30 minute period in such a manner, with cooling, and then heating, that the redaction temperature was maintained at about 70°C until the reaction was complete as determined by % NCO.
- The following examples, which are illustrative rather than limiting or delineative of the scope of the invention, serve to describe the novel compounds, their method of preparation, and their properties.
- The following runs demonstrate the effect of reactive diluent and the percentage thereof in the binder of the coated abrasive of the present invention.
- In the following runs, to a mixture containing 100 g of monomer and reactive diluent in the ratios as shown in Table I below was added 250 g A1203 (20 micrometers) which had been pretreated with 2% gamma-methacryloxy propyl trimethoxysilane (Z-6030), based on the weight of A1203. The resulting composition was coated at 1 mil thickness on ethylene acrylic acid primed polyethylene terephthalate film. The coated film was subjected to electron beam radiation at 250 kev, 8 Mrad.
-
- The coated abrasive of the present invention exhibited improved results according to the second fine test procedure, as the cut was dramatically increased while finish and abrasive wear continued to be acceptable.
- This example demonstrates the effect of coupling agent on the coated abrasive of the present invention.
- In the following runs, to a mixture containing 100 g of monomer and reactive diluent in the ratio 1:1 (by weight) was added 150 g A1203 (12 micrometers). In the control run, no coupling agent was employed. In the second run 1% by weight of coupling agent, based on weight of abrasive grains, was used to pretreat the A1203 abrasive. The compositions were knife coated at 1 mil thickness on ethylene acrylic acid primed polyethylene terephthalate film. The coated film was subjected to electron beam radiation at 240 Kev, 9 Mrad. The performance characteristics of the coated abrasive thus prepared are shown in Table II.
- The addition of a coupling agent resulted in an improvement in the durability, and, consequently, the performance of the coated abrasive as well as a reduction in the viscosity of the coating composition.
- This example demonstrates the preferred combination of monomer, reactive diluent, coupling agent, and abrasive grain. In the following runs, the monomers, and reactive diluents were blended, and abrasive grains pretreated with gamma-methacryloxypropyltrimethoxysilane coupling agent (Z6030) was introduced into the mixture. Dyes were also utilized in the mixtures so that the size of the abrasive grains in each run could be identified. The ratios of ingredients are set forth in Table III.
- The compositions were knife coated at 1 mil thickness on ethylene acrylic acid primed polyethylene terephthalate film. The coated film was subjected to electron beam radiation at 250 Kev, 8 Mrad.
-
- Various modifications and alterations of this invention will become apparent to those skilled in the art without departing from the scope and spirit of this invention, and it should be understood that this invention is not to be unduly limited to the illustrative embodiments set forth herein.
Claims (14)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US80900385A | 1985-12-16 | 1985-12-16 | |
US809003 | 1991-12-17 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0227394A2 true EP0227394A2 (en) | 1987-07-01 |
EP0227394A3 EP0227394A3 (en) | 1987-11-11 |
EP0227394B1 EP0227394B1 (en) | 1991-05-02 |
Family
ID=25200316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86309714A Expired - Lifetime EP0227394B1 (en) | 1985-12-16 | 1986-12-12 | Coated abrasive suitable for use as a lapping material |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0227394B1 (en) |
JP (1) | JP2655570B2 (en) |
KR (1) | KR950001983B1 (en) |
CA (1) | CA1263240A (en) |
DE (1) | DE3679048D1 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0321230A2 (en) * | 1987-12-14 | 1989-06-21 | Minnesota Mining And Manufacturing Company | Improved resin systems for coated products, and method |
EP0396150A2 (en) * | 1989-05-05 | 1990-11-07 | Norton Company | Coated abrasive material and method of making same |
EP0520643A2 (en) * | 1991-06-26 | 1992-12-30 | Minnesota Mining And Manufacturing Company | Process for manufacturing abrasive tape |
WO1994015751A1 (en) * | 1993-01-15 | 1994-07-21 | Minnesota Mining And Manufacturing Company | Flexible bonded abrasive articles, methods of production and use |
EP0747455A1 (en) * | 1995-06-06 | 1996-12-11 | Norton Company | Friction coating for film backings |
WO1997026114A1 (en) * | 1996-01-22 | 1997-07-24 | Micron Technology, Inc. | A polishing pad and a method for making a polishing pad with covalently bonded particles |
US5938801A (en) * | 1997-02-12 | 1999-08-17 | Micron Technology, Inc. | Polishing pad and a method for making a polishing pad with covalently bonded particles |
CN110549258A (en) * | 2018-06-01 | 2019-12-10 | 东莞市中微纳米科技有限公司 | Polishing sheet and preparation method thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2276820A4 (en) | 2008-04-18 | 2013-12-25 | Saint Gobain Abrasives Inc | High porosity abrasive articles and methods of manufacturing same |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2200773A5 (en) * | 1972-09-26 | 1974-04-19 | Reichhold Albert Chemie Ag | Waterproof abrasive sheets mfr - by coating fibrous substrate with harden-able binder resin and hardening by electron beam radiation |
US4047903A (en) * | 1972-09-26 | 1977-09-13 | Hoechst Aktiengesellschaft | Process for the production of abrasives |
US4289233A (en) * | 1976-12-06 | 1981-09-15 | Applied Plastics Co., Inc. | Packaging of mutually reactive substances |
GB2087263A (en) * | 1980-10-08 | 1982-05-26 | Kennecott Corp | Resin systems for high energy electron curable resin coated webs |
US4389433A (en) * | 1980-12-04 | 1983-06-21 | Rca Corporation | Sulfur dioxide cured coatings |
GB2137118A (en) * | 1983-03-28 | 1984-10-03 | Konishiroku Photo Ind | Method of producing support for photographic paper |
DE3317882A1 (en) * | 1983-05-17 | 1984-11-22 | Merck Patent Gmbh, 6100 Darmstadt | RADIATION-curable BINDING SYSTEMS, METHOD FOR THEIR USE AND COVERS PRODUCED THEREOF |
US4485226A (en) * | 1983-05-18 | 1984-11-27 | Bayer Aktiengesellschaft | Process for the production of compounds containing isocyanurate groups and olefinic double bonds, the compounds obtainable by this process and their use as binders or binder component in coating compositions |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6016365A (en) * | 1983-07-01 | 1985-01-28 | Fujikura Kasei Kk | Composite material for polishing |
-
1986
- 1986-11-18 CA CA000523191A patent/CA1263240A/en not_active Expired
- 1986-12-12 DE DE8686309714T patent/DE3679048D1/en not_active Expired - Fee Related
- 1986-12-12 EP EP86309714A patent/EP0227394B1/en not_active Expired - Lifetime
- 1986-12-15 JP JP61298591A patent/JP2655570B2/en not_active Expired - Fee Related
- 1986-12-15 KR KR1019860010720A patent/KR950001983B1/en not_active IP Right Cessation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2200773A5 (en) * | 1972-09-26 | 1974-04-19 | Reichhold Albert Chemie Ag | Waterproof abrasive sheets mfr - by coating fibrous substrate with harden-able binder resin and hardening by electron beam radiation |
US4047903A (en) * | 1972-09-26 | 1977-09-13 | Hoechst Aktiengesellschaft | Process for the production of abrasives |
US4289233A (en) * | 1976-12-06 | 1981-09-15 | Applied Plastics Co., Inc. | Packaging of mutually reactive substances |
GB2087263A (en) * | 1980-10-08 | 1982-05-26 | Kennecott Corp | Resin systems for high energy electron curable resin coated webs |
US4389433A (en) * | 1980-12-04 | 1983-06-21 | Rca Corporation | Sulfur dioxide cured coatings |
GB2137118A (en) * | 1983-03-28 | 1984-10-03 | Konishiroku Photo Ind | Method of producing support for photographic paper |
DE3317882A1 (en) * | 1983-05-17 | 1984-11-22 | Merck Patent Gmbh, 6100 Darmstadt | RADIATION-curable BINDING SYSTEMS, METHOD FOR THEIR USE AND COVERS PRODUCED THEREOF |
US4485226A (en) * | 1983-05-18 | 1984-11-27 | Bayer Aktiengesellschaft | Process for the production of compounds containing isocyanurate groups and olefinic double bonds, the compounds obtainable by this process and their use as binders or binder component in coating compositions |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0321230B1 (en) * | 1987-12-14 | 1993-10-27 | Minnesota Mining And Manufacturing Company | Improved resin systems for coated products, and method |
EP0321230A2 (en) * | 1987-12-14 | 1989-06-21 | Minnesota Mining And Manufacturing Company | Improved resin systems for coated products, and method |
EP0396150A2 (en) * | 1989-05-05 | 1990-11-07 | Norton Company | Coated abrasive material and method of making same |
EP0396150A3 (en) * | 1989-05-05 | 1992-02-26 | Norton Company | Coated abrasive material and method of making same |
US5271964A (en) * | 1991-06-26 | 1993-12-21 | Minnesota Mining And Manufacturing Company | Process for manufacturing abrasive tape |
EP0520643A3 (en) * | 1991-06-26 | 1993-05-05 | Minnesota Mining And Manufacturing Company | Process for manufacturing abrasive tape |
EP0520643A2 (en) * | 1991-06-26 | 1992-12-30 | Minnesota Mining And Manufacturing Company | Process for manufacturing abrasive tape |
WO1994015751A1 (en) * | 1993-01-15 | 1994-07-21 | Minnesota Mining And Manufacturing Company | Flexible bonded abrasive articles, methods of production and use |
EP0747455A1 (en) * | 1995-06-06 | 1996-12-11 | Norton Company | Friction coating for film backings |
WO1997026114A1 (en) * | 1996-01-22 | 1997-07-24 | Micron Technology, Inc. | A polishing pad and a method for making a polishing pad with covalently bonded particles |
US5823855A (en) * | 1996-01-22 | 1998-10-20 | Micron Technology, Inc. | Polishing pad and a method for making a polishing pad with covalently bonded particles |
US5879222A (en) * | 1996-01-22 | 1999-03-09 | Micron Technology, Inc. | Abrasive polishing pad with covalently bonded abrasive particles |
US5938801A (en) * | 1997-02-12 | 1999-08-17 | Micron Technology, Inc. | Polishing pad and a method for making a polishing pad with covalently bonded particles |
CN110549258A (en) * | 2018-06-01 | 2019-12-10 | 东莞市中微纳米科技有限公司 | Polishing sheet and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2655570B2 (en) | 1997-09-24 |
EP0227394A3 (en) | 1987-11-11 |
DE3679048D1 (en) | 1991-06-06 |
KR950001983B1 (en) | 1995-03-08 |
JPS62157770A (en) | 1987-07-13 |
CA1263240A (en) | 1989-11-28 |
EP0227394B1 (en) | 1991-05-02 |
KR870005750A (en) | 1987-07-07 |
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