US20060265967A1 - Abrasive articles and methods of making and using the same - Google Patents
Abrasive articles and methods of making and using the same Download PDFInfo
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- US20060265967A1 US20060265967A1 US11/136,692 US13669205A US2006265967A1 US 20060265967 A1 US20060265967 A1 US 20060265967A1 US 13669205 A US13669205 A US 13669205A US 2006265967 A1 US2006265967 A1 US 2006265967A1
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- abrasive article
- coated abrasive
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- 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
- B24D11/02—Backings, e.g. foils, webs, mesh fabrics
Definitions
- Vulcanized fiber has been in commerce since the 19 th century.
- Coated abrasive articles typically have an abrasive layer affixed to a backing.
- Vulcanized fiber has been used as a backing material for coated abrasive articles for more than 60 years.
- One well-recognized problem of using vulcanized fiber backings in abrasive articles is shape distortion (e.g., curling or cupping) of the coated abrasive article due to changes in environmental moisture content (e.g., humidity). Shape distortion may occur, for example, during manufacturing, during storage, or during use. Further, the shape distortion may occur toward and/or away from the abrasive layer.
- An example of such distortion of a prior art coated abrasive article having a vulcanized fiber backing is shown in FIG.
- the coated abrasive article exhibits curling directed away from the abrasive layer. If excessive shape distortion occurs during manufacturing the coated abrasive article, then it is typically discarded as scrap material. Further, if excessive shape distortion occurs during storage, or in use, it typically results in product complaints, reduced product sales, and/or reduced product performance.
- vulcanized fiber backings are still used today in the commercial manufacture of coated abrasive articles primarily.
- the major coated abrasives manufacturers each market coated abrasive products with vulcanized fiber backings that are prone to humidity problems, even though alternative moisture insensitive and dimensionally stable backings for coated abrasive articles are known. Accordingly, there remains a need in the coated abrasives industry for coated abrasive products with vulcanized fiber backings that are economical to manufacture and that are not prone to unacceptable levels of shape distortion with changes in humidity levels.
- the present invention provides a coated abrasive article comprising a vulcanized fiber backing having first and second opposed major surfaces, an abrasive layer affixed to the first major surface, and a backsize affixed to the second major surface, wherein the backsize has a dry basis weight of from 8 to 90 grams per square meter of the coated abrasive article, and wherein the backsize comprises a reaction product of components selected from the group consisting of curable latex emulsions, phenolic resins, and combinations thereof.
- the present invention provides a method of abrading a surface of a workpiece, the method comprising: providing a coated abrasive article according to the present invention, frictionally contacting the abrasive layer with a surface of the workpiece, and moving at least one of the abrasive layer and the surface of the workpiece relative to the other to abrade at least a portion of the surface of the workpiece.
- the present invention provides a method of making a coated abrasive article, the method comprising:
- a vulcanized fiber backing having first and second opposed major surfaces
- the backsize precursor comprises at least one material selected from the group consisting of curable latex emulsions, phenolic resins, and combinations thereof;
- Coated abrasive articles according to the present invention typically exhibit industry acceptable levels of shape distortion with changes in humidity. Surprisingly, it is also found that such articles enable attachment of mechanical fasteners to the backsize and hence the vulcanized fiber backing by a welding process, whereas before the present invention this was not possible.
- FIG. 1 is a photograph of a coated abrasive disc of the prior art
- FIG. 2 is a cross-sectional side view of an exemplary coated abrasive article according to one embodiment of the present invention
- FIG. 3 is a cross-sectional side view of an exemplary coated abrasive article according to one embodiment of the present invention.
- FIG. 4 is a perspective view of an exemplary coated abrasive disc with a welded mechanical fastener according to one embodiment of the present invention.
- FIG. 5 is a photograph of a coated abrasive disc prepared according to Example 1.
- coated abrasive articles have abrasive particles affixed to a backing. More typically, coated abrasive articles comprise a backing having two major opposed surfaces and an abrasive layer affixed to one major surface of the backing.
- the abrasive layer typically comprises abrasive particles and a binder, wherein the binder serves to secure the abrasive particles to the backing.
- the coated abrasive article has an abrasive layer comprising a make layer, a size layer, and abrasive particles.
- a make layer comprising a first binder precursor is applied to one major surface of the backing, and optionally partially cured. Abrasive particles are then at least partially embedded into the make layer (e.g., via electrostatic coating), and the first binder precursor is sufficiently cured (i.e., crosslinked) to secure the particles to the make layer.
- a size layer comprising a second binder precursor is then applied over the make layer and abrasive particles, followed by curing of the binder precursors.
- Such coated abrasive articles may further comprise an optional supersize layer disposed on at least a portion of the abrasive layer. If present, the supersize layer typically includes grinding aids and/or anti-loading materials.
- the coated abrasive article has an abrasive layer affixed to one major surface of a backing, wherein the abrasive layer is provided by applying a slurry comprised of binder precursor and abrasive particles onto a major surface of a backing, and then curing the binder precursor.
- the backing comprises vulcanized fiber, a dense material of partially regenerated cellulose in which the fiber structure is retained and which is typically calendered to provide a relatively smooth surface.
- Vulcanized fiber is widely available from commercial sources such as, for example, Franklin Fibre—Lamitex Corporation (Wilmington, Del.) or Yangmin Ind. Trade Co., Ltd. (Sanmenxia, Henan, China).
- vulcanized fiber backing useful-for preparing coated abrasive articles according to the present invention has a thickness in a range of from 0.02 to 5 millimeters, for example, from 0.05 to 2.5 millimeters or from 0.1 to 1 millimeter, although thinner and thicker vulcanized paper backings may also be used.
- the density of the vulcanized fiber is typically in a range of from 0.9 to 1.5 grams per cubic centimeter, although higher and lower density vulcanized fiber may also be used.
- At least a portion, typically substantially all, of one major surface of the vulcanized fiber backing is coated with curable resin, which then is at least partially cured, for example, by drying and heating to provide a backsize on the vulcanized fiber backing.
- Coating of the vulcanized fiber backing with the curable material may be achieved by any suitable coating method including, for example, roll coating, bar coating, knife coating, kiss coating, or spraying.
- the curable material should typically be coated onto the vulcanized fiber such that it is distributed over at least a substantial portion of the body of the vulcanized fiber, typically in a substantially uniform manner, although this is not a requirement. For example, it will be recognized that a minor amount of local variations or interruptions in the distribution (e.g., coating voids) may be tolerated without significant adverse effects.
- the backsize treated vulcanized fiber backing may optionally further comprise additional backing treatments a presize (i.e., a layer affixed to the backing on the major surface having the abrasive layer), a tie layer (i.e., a layer between the abrasive layer and the major surface to which the abrasive layer is affixed), a saturant (i.e., a backing treatment applied by a process that includes saturating the backing with the saturant) and/or a subsize treatment.
- a subsize is similar to a saturant, except that it is applied to a previously treated backing.
- An antistatic material may be included in any of these backing treatments.
- an antistatic material can reduce the tendency of the coated abrasive article to accumulate static electricity when sanding wood or wood-like materials. Additional details regarding antistatic backings and backing treatments can be found in, for example, U.S. Pat. No. 5,108,463 (Buchanan); U.S. Pat. No. 5,137,542 (Buchanan et al.); U.S. Pat. No. 5,328,716 (Buchanan); and U.S. Pat. No. 5,560,753 (Schnabel et al.); the disclosures of which are incorporated herein by reference.
- the backsize has a dry basis weight of from 8 to 90 grams per square meter, typically selected according to the composition of the backsize.
- the backsize typically has a dry basis weight of from 8 to 25 grams per square meter, 10 to 20 grams per square meter, or even a basis weight of from 12 to 17 grams per square meter.
- the backsize typically has a dry basis weight of from 15 to 90 grams per square meter, 45 to 55 grams per square meter, or even a basis weight of from 50 to 55 grams per square meter.
- the backsize treated vulcanized fiber backing will have a thickness in a range of from 0.15 to 2.0 millimeters, for example, 0.5 to 1.3 millimeters, or even 0.8-0.9 millimeters, although thicker and thinner backsize treated vulcanized fiber backings may also be used.
- the backsize comprises at least one material that is a reaction product of at least one curable material selected from the group consisting of phenolic resins, curable latex emulsions, and combinations thereof.
- the reinforcing material may include one or more optional additives such as, for example, fillers, antistatic agents, antioxidants, or colorants.
- phenolic resin includes phenol-formaldehyde resins as well as resins comprising other phenol-derived compounds and aldehydes.
- a portion of the phenol can be substituted with one or more other phenols such as resorcinol, m-cresol, 3,5-xylenol, t-butylphenol and p-phenylphenol.
- a portion of the formaldehyde can be substituted with other aldehyde groups such as acetaldehyde, chloral, butyraldehyde, furfural, or acrolein.
- phenolic resins examples include resole-phenolic resins and novolak phenolic resins.
- Resole phenolic resins have a molar ratio of formaldehyde to phenol of greater than or equal to one to one, typically in a range of from 1.5:1.0 to 3.0:1.0.
- Novolak phenolic resins have a molar ratio of formaldehyde to phenol of less than one to one.
- Typical resole phenolic resins contain a base catalyst.
- the presence of a basic catalyst speeds up the reaction or polymerization rate of the phenolic resin.
- the pH of resole phenolic resins is typically from 6 to 12, more typically from 7 to 10, and even more typically from 7 to 9.
- suitable basic catalysts include sodium hydroxide, potassium hydroxide, calcium hydroxide, magnesium hydroxide, barium hydroxide, and combinations thereof.
- Typical catalysts for the reaction of formaldehyde with phenol are chosen from group I and II metal salts, generally because of their high reactivity and low cost. Amines are also used to catalyze the phenol/aldehyde reaction.
- the amount of basic catalyst is typically 5 percent by weight or less, more typically 2 percent by weight or less, and even more typically 1 percent by weight or less based on the weight of the phenolic resin.
- Resole phenolic resins are usually made from phenol and formaldehyde.
- Phenolic resins are typically coated as a solution with water and/or organic solvent (e.g., alcohol). Typically, the solution includes about 70 percent to about 85 percent solids, although other concentrations may be used. If the solids content is very low, then more energy is required to remove the water and/or solvent. If the solids content is very high, then the viscosity of the resulting phenolic resin is too high which typically leads to processing problems.
- organic solvent e.g., alcohol
- curable latex emulsions examples include those curable latex emulsions derived from styrene, butadiene, acrylonitrile, neoprene, polyvinyl acetate, acrylate esters acrylamides, and copolymers thereof. Mixtures of curable latex emulsions may also be used.
- curable latex emulsions include, for example, those available under the trade designations “RHOPLEX” and “ACRYSOL” from Rohm and Haas Company (Philadelphia, Pa.); “FLEXCRYL” and “VALTAC” from Air Products & Chemicals Inc. (Allentown, Pa.); “SYNTHEMUL”, “TYCRYL”, and “TYLAC” from Dow Reichold Specialty Latex, LLC (Research Triangle Park, N.C.), “HYCAR”, “CARBOCURE”, “GOOD-RITE”, “SANCURE” and “VYCAR” from NOVEON (Cleveland, Ohio); “CHEMIGUM” commercially available from Goodyear Tire and Rubber Co.
- the latex is self-curing (i.e., self-crosslinking), it is typically used in combination with at least one additive (e.g., a crosslinker) that facilitates curing or it may also be used in combination with another curable material.
- a crosslinker e.g., a crosslinker
- Examples of commercially available self-curing latexes include those emulsions having the trade designations “CARBOCURE TSR-72” and “CARBOCURE TSR-201”; styrene butadiene emulsions having the trade designation “GOOD-RITE SB-1168”, “GOOD-RITE SB-0706”, “GOOD-RITE 1800x73”; a polyurethane dispersion having the trade designation “SANCURE AU-4010” (acrylic urethane hybrid); a polyvinyl acetate emulsion having the trade designation “VYCAR VA-0450”; and a pvc-acrylic copolymer having the trade designation “VYCAR TN-810”; all marketed by Noveon, Cleveland, Ohio.
- the curable material may optionally contain one or more curatives, for example, as described above, or in addition thereto.
- the choice of curative is typically determined by the curable material selected and may include, for example, acid, base, photocatalyst, hardeners, crosslinkers (e.g., polyepoxides, melamine resins, polyaziridines, polyvalent metal ions, dicyandiamide, urea-formaldehyde resins, and mixtures thereof).
- the amount of optional added curative is typically less than about 5 percent of the dry weight of the latex that it is intended to cure (i.e., crosslink), although higher amounts may be used. Examples of curatives for various latexes may be found, for example, in U.S. Pat. No. 6,306,514 (Weikel et al.).
- curatives for latexes include, for example, melamine resins such as those available from Cytec Industries, West Paterson, N.J. under the trade designation “AEROTEX” (e.g., “AEROTEX M-3”, “AEROTEX 3730”, and “AEROTEX 3030”), glycolurils available from Cytec Industries under the trade designations “CYMEL 1172” and “CYMEL 1171”, and alkylated melamine resins such as those available from Cytec Industries under the trade designations “CYMEL 300”, “CYMEL 303”, “CYMEL 373” and “CYMEL 350”; polyaziridines such as those available from Bayer Corporation, Pittsburgh, Pa., under the trade designation “XAMA” (e.g., “XAMA-7” and “XAMA-2”); waterborne aliphatic epoxies such as those available from Resolution Performance Products, Houston, Tex., under the trade designation “EPI-REZ”; melamine-formaldehyde resins
- coated abrasive articles typically have an abrasive layer affixed to a backing.
- the abrasive layer comprises make and size layers and abrasive particles or, alternatively, a layer of abrasive particles dispersed in a binder.
- the coated abrasive article has an abrasive layer comprising make and size layers and abrasive particles as shown, for example, in FIG. 2 .
- exemplary coated abrasive article 200 comprises vulcanized fiber backing 212 having first and second opposed major surfaces 231 , 232 .
- Backsize 213 is affixed to second major surface 232 .
- abrasive layer 230 comprising: make layer 216 in which are embedded abrasive grits 218 , and size layer 217 which overlays and is affixed to make layer 216 and abrasive grits 218 .
- Optional supersize 219 overlays size layer 217 .
- the basis weight of the make layer utilized may depend, for example, on the intended use(s), type(s) of abrasive particles, and nature of the coated abrasive article being prepared, but generally will be in the range of from 1, 2, or 5 to 20, 25, 400, or even 600 grams per square meter.
- the make layer is generally applied as a make layer precursor that upon subsequent solidification (e.g., by curing or cooling) forms a layer of binder material of sufficient strength to secure abrasive particles to the backing.
- the make layer precursor may be applied by any known coating method for applying a make layer precursor to a backing, including, for example, roll coating, extrusion die coating, curtain coating, knife coating, gravure coating, and spray coating.
- make layer precursors include curable materials comprising phenolics, aminoplasts, poly(meth)acrylates, polyepoxides, polyisocyanates, hide glue, and combinations thereof.
- abrasive particles are deposited onto the make layer.
- Exemplary useful abrasive particles include fused aluminum oxide based materials such as aluminum oxide, ceramic aluminum oxide (which may include one or more metal oxide modifiers and/or seeding or nucleating agents), and heat-treated aluminum oxide, silicon carbide, co-fused alumina-zirconia, diamond, ceria, titanium diboride, cubic boron nitride, boron carbide, garnet, flint, emery, sol-gel derived abrasive particles, and blends thereof.
- Examples of sol-gel abrasive particles include those described U.S. Pat. No. 4,314,827 (Leitheiser et al.); U.S. Pat. No.
- the abrasive particles may be in the form of, for example, individual particles, agglomerates, abrasive composite particles, and mixtures thereof.
- Exemplary agglomerates are described, for example, in U.S. Pat. No. 4,652,275 (Bloecher et al.) and U.S. Pat. No. 4,799,939 (Bloecher et al.), the disclosures of which are incorporated herein by reference. It is also within the scope of the present invention to use diluent erodible agglomerate grains as described, for example, in U.S. Pat. No. 5,078,753 (Broberg et al.), the disclosure of which is incorporated herein by reference.
- Abrasive composite particles comprise abrasive grains in a binder.
- Exemplary abrasive composite particles are described, for example, in U.S. Pat. No. 5,549,962 (Holmes et al.), the disclosure of which is incorporated herein by reference.
- Coating weights for the abrasive particles may depend, for example, on the specific coated abrasive article desired, the process for applying the abrasive particles, and the size of the abrasive particles, but typically range from 1 to 2000 g/m 2 .
- the basis weight of the size layer will also necessarily vary depending on the intended use(s), type(s) of abrasive particles, and nature of the coated abrasive article being prepared, but generally will be in the range of from 1 or 5 g/m 2 to 300, or even 800 g/m 2 , or more.
- the size layer is generally applied as a size layer precursor that upon subsequent solidification (e.g., by curing or cooling) forms a layer of binder material of sufficient strength to secure the abrasive particles to the make layer.
- the size layer precursor may be applied by any known coating method for applying a size layer precursor to a backing, including, for example, roll coating, extrusion die coating, curtain coating, knife coating, gravure coating, and spray coating.
- size layer precursors include curable materials comprising at least one of phenolic resins, aminoplasts, poly(meth)acrylates, polyepoxides, polyisocyanates, hide glue, urea-formaldehyde resins, melamine-formaldehyde resins, and combinations thereof.
- coated abrasive articles comprising abrasive particles and make and size layers, and optional supersize are well known and are described, for example, in U.S. Pat. No. 4,734,104 (Broberg); U.S. Pat. No. 4,737,163 (Larkey); U.S. Pat. No. 5,203,884 (Buchanan et al.); U.S. Pat. No. 5,152,917 (Pieper et al.); U.S. Pat. No. 5,378,251 (Culler et al.); U.S. Pat. No. 5,417,726 (Stout et al.); U.S. Pat. No.
- the coated abrasive article has an abrasive layer comprising a layer of abrasive particles dispersed in a binder as shown, for example, in FIG. 3 .
- exemplary coated abrasive article 300 comprises vulcanized fiber backing 312 having first and second opposed major surfaces 331 , 332 .
- Backsize 313 is affixed to second major surface 332 .
- Optional presize 315 is affixed to major surface 331 .
- abrasive layer 330 Overlaying optional presize 315 and affixed to backing 312 is abrasive layer 330 , which comprises a plurality of abrasive grits 318 distributed throughout binder 309 .
- the abrasive layer comprises a dispersion of abrasive particles in a binder (typically coated as a slurry of abrasive particles in a binder precursor).
- Slurry coating techniques are well known in the abrasive art, and include those described, for example, in U.S. Pat. No. 5,378,251 (Culler et al.); U.S. Pat. No. 5,942,015 (Culler et al.); and U.S. Pat. No. 6,277,160 (Stubbs et al.); the disclosures of which are incorporated herein by reference.
- binder precursors examples include curable materials comprising phenolics, aminoplasts, poly(meth)acrylates, polyepoxides, polyisocyanates, and combinations thereof.
- Abrasive particles used in this embodiment include all of those previously listed hereinabove.
- Coated abrasive articles according to the present invention can be converted, for example, into belts, tapes, rolls, discs (including perforated discs), and/or sheets.
- coated abrasives according to the present invention typically have improved cut under at least some conditions (e.g., under elevated humidity conditions) as compared to corresponding coated abrasives of the prior art.
- a spliceless belt may also be formed as described, for example, in U.S. Pat. No. 5,573,619 (Benedict et al.), the disclosure of which is incorporated herein by reference.
- coated abrasive discs according to the present invention may have a mechanical fastener affixed to the vulcanized paper backing.
- exemplary coated abrasive disc 400 has mechanical fastener 490 affixed to backsize-coated major surface 432 of vulcanized fiber backing 412 of abrasive disc 420 .
- Abrasive disc 420 may be, for example, a disc made from either of coated abrasive articles 200 or 300 .
- Suitable techniques for attaching the mechanical fastener include, for example, adhesives, rivets, welding.
- Exemplary welding techniques include, for example, ultrasonic welding, infrared welding, vibration welding, and frictional welding (including spin welding). Welding may also be accomplished as a stepwise process in which at least a portion of the thermoplastic is heated until it is at least partially softened or melted, and then the softened or melted thermoplastic is bonded to the abrasive article.
- at least spin welding is typically simple, effective, and convenient. It is surprising found that mechanical fasteners can be successfully spin welded to the backsize coated vulcanized fiber backings, while this is not typically possible using vulcanized fiber backings. Further details concerning mechanical fasteners and welding techniques may be found, for example, in commonly assigned U.S. Ser. No. 10/828,119 (Fritz et al.), filed Apr. 20, 2004, the disclosure of which is incorporated herein by reference.
- Coated abrasive articles according to the present invention are useful for abrading a workpiece.
- One such method includes frictionally contacting at least a portion of the abrasive layer of a coated abrasive article with at least a portion of a surface of the workpiece, and moving at least one of the coated abrasive article or the workpiece relative to the other to abrade at least a portion of the surface.
- workpiece materials include metal, metal alloys, exotic metal alloys, ceramics, glass, wood, wood-like materials, composites, painted surfaces, plastics, reinforced plastics, stone, and/or combinations thereof.
- the workpiece may be flat or have a shape or contour associated with it.
- specific workpieces include metal components, plastic components, particleboard, camshafts, crankshafts, furniture, and turbine blades.
- Coated abrasive articles according to the present invention may be used by hand and/or used in combination with a machine. At least one or both of the coated abrasive article and the workpiece is generally moved relative to the other when abrading. Abrading may be conducted under wet or dry conditions. Exemplary liquids for wet abrading include water, water containing conventional rust inhibiting compounds, lubricant, oil, soap, and cutting fluid. The liquid may also contain defoamers, degreasers, and/or the like.
- Vulcanized Fiber Discs used in the Examples had a diameter of 7 inches (18 cm), and had a center hole of 7 ⁇ 8-inch.
- ABBRE- VIATION DESCRIPTION VF vulcanized fiber web 33.5 mils thickness, obtained under the trade designation “DYNOS FIBRE” from H. T. Troplast AG, Troisdorf, Germany.
- This product is supplied with a green-colored back side and a brown-colored front side.
- AR1 acrylic polymer emulsion, 35 wt. % solids obtained under the trade designation “CARBOCURE TSR 72” from Noveon, Inc., Cleveland, Ohio SBR styrene/butadiene/acrylonitrile copolymer, obtained under the trade designation “STYRONAL NX 4681” from BASF Corporation, Ludwigshafen, Germany
- AR2 acrylic emulsion 49 wt.
- CACO calcium carbonate filler obtained under the trade designation “HUBERCARB Q325” from J. M. Huber Corporation, Fairmount, Georgia CRY filler, obtained under the trade designation “CRYOLITE TYPE RTN-C” from Koppers Trading, Pittsburgh, Pennsylvania RIO red iron oxide obtained from Elementis Pigments Inc., East St.
- the abrasive discs to be evaluated were removed from the restricting bales, and laid out individually (abrasive side down) on the shelves of a chamber controlled to 15% RH (relative humidity), 24° C. for 48 hours.
- RH relative humidity
- Four discs per example of material were studied.
- the shape of each disc was measured using a laser height gauge capable of measuring to the nearest 10 micrometers (Model LG10, obtained from Banner Engineering, Minneapolis, Minn.).
- the laser device was used to measure the height of individual discs in four points: the two lowest points and the two highest points.
- the difference between the average highest and lowest values was reported for each disc as Delta Height. Net shape out-of-plane toward the backing side was designated positive (+).
- Net shape out-of-plane toward the abrasive side was reported as negative ( ⁇ ). This procedure was repeated for 30%, 45%, 60% and 75% RH environments, the temperature being held at 24° C. The reported number in each case is an average of the difference in measurements taken on four replicate discs.
- abrasive discs were removed from the bales and laid out individually (abrasive side down) to precondition in a chamber controlled to 45% RH, 24° C. After 48 hours preconditioning, the shape of each disc was measured with the laser as described in “Shape Measurements Procedure A”, above. Four of the discs were then placed in a chamber controlled to 20% RH, 24° C., and the remaining four placed in a chamber controlled to 60% RH, 24° C. After 48 hours, the discs were taken out of the chambers eight at a time and measured with the laser gauge. The reported number in each case is an average of the measurements taken on four replicate discs. Four additional measurements were made after each 48-hour period for a total test duration of 10 days.
- the abrasive discs to be evaluated were removed from the restricting bales and the shape (i.e., the deviation from planarity) of each disc was measured using a laser height gauge capable of measuring to the nearest 10 micrometers (Model LG10, obtained from Banner Engineering, Minneapolis, Minn.). Each disc was placed on a table with the center hole most distal from the table. The height of the center hole from the table was measured using the laser height gauge. Net shape out-of-plane toward the backing side was designated positive (+). Net shape out-of-plane toward the abrasive side was reported as negative ( ⁇ ).
- the Grinding Test was designed to measure the cut rate of the coated abrasive disc. Test discs were conditioned at 45% RH and 24° C. for 2 days. Prior to testing, half of these pre-conditioned discs were then placed into a 20% RH, 24° C. and the other half into a 60% RH, 24° C. environment for one week prior to testing. Each finally conditioned abrasive disc was used to grind the face of a 1.25 cm by 18 cm 1018 mild steel workpiece. The grinder used was a constant load hydraulic disc grinder. The constant load between the workpiece and the abrasive disc was provided by a load spring.
- the back-up pad for the grinder was an aluminum back-up pad, beveled at approximately 7 degrees, extending from the edge and in towards the center 3.5 cm.
- the disc was secured to the aluminum pad by a retaining nut and was driven at 5,500 rpm.
- the load between the back-up pad and disc and workpiece was about 6.8 kg.
- Each disc was used to grind a separate workpiece for each of 15 60-second intervals.
- the initial cut was the amount of metal removed in the first 60 seconds of grinding.
- the final cut was the amount of metal removed during the 15 th 60-second interval. Unless otherwise noted, total cut is the cumulative amount of metal removed during the test. Initial, final, and total cut in grams are reported.
- Grinding Test 2 was also designed to measure the cut rate of the coated abrasive disc.
- Test discs were conditioned at 45% RH and 24° C. for 2 days. Each abrasive disc was used to grind the face of a 1.25 cm by 18 cm 1018 mild steel workpiece.
- the grinder used was a constant load hydraulic disc grinder. The constant load between the workpiece and the abrasive disc was provided by a load spring.
- the back-up pad for the grinder was an aluminum back-up pad, beveled at approximately 7 degrees, extending from the edge and in towards the center 3.5 cm.
- the disc was secured to the aluminum pad by a retaining nut and was driven at 5,500 rpm. The load between the back-up pad and disc and workpiece was about 5.9 kg.
- Each disc was used to grind a workpiece for 60-second intervals. At the end of each interval the workpiece was changed. The cut (the amount of metal removed) was measured after each 60 seconds of grinding. The end of the test was defined as when the cut was less than 40 grams in a 60-second interval. Unless otherwise noted, total cut is the cumulative amount of metal removed during the test. Total cut in grams (average of six discs) is reported.
- Examples 1-4 and Comparative Example A illustrate the effects of composition and wet add-on of the various backsize compositions on the shape stability of resulting abrasive discs. Composition and wet add-on of the backsize for these examples are reported in Table II (below). TABLE II Example AR1 SBR PM1 1 35.6 0 0 2 21.6 0 0 3 0 24.5 0 4 0 0 38.9 Comparative Example A 0 0 0 0
- Example 1 was prepared by applying via a 3-roll coater AR1 to one side of a 305 mm wide VF web.
- the backsize coating was allowed to dry for 3 minutes in an oven set at 85° C. to a dry weight of about 12.4 grams per square meter (gsm).
- the backsize treated web was wound into a roll and allowed to condition 7 to 10 days in a 50% RH environment.
- An abrasive coating consisting of 184 gsm of a make coating (PM2), 552 gsm particle coating (AP), and 339 gsm of a size coating (PM3) was applied to the conditioned, backsize treated web and cured. Short pieces of cured abrasive web were wound into loose rolls and steamed for 1 hour at 65° C.
- Example 2 was prepared as in Example 1, except the weight of AR1 was 21.6 gsm (drying down to about 7.5 gsm).
- Example 3 was prepared as in Example 1, except that SBR was applied to the vulcanized fiber web at a weight of 24.5 gsm (drying down to about 12.5 gsm).
- Example 4 was prepared as in Example 1, except that PM1 was applied to the vulcanized fiber web at a weight of 38.9 gsm (drying down to about 20.8 gsm). The oven temperature was increased to 121° C.
- Comparative Example A was a control example, prepared according to Example 1, but having no backsize applied to the vulcanized fiber web.
- Examples 1-4 and Comparative Example A were evaluated for shape change according to Shape Measurement Procedure A. The results in mm are reported in Table III (below). A coated abrasive disc prepared according to Example I is shown in FIG. 5 . TABLE III EXAMPLE DELTA HEIGHT, mm 1 13.88 2 24.16 3 23.15 4 19.63 Comparative Example A 25.25
- Examples 5-11 and Comparative Example B illustrate the effects of composition and wet add-on of the various backsize compositions on the shape stability of resulting abrasive discs. Composition and wet add-on of the backsize for these examples are reported below.
- Example 5 was prepared as in Example 4, except that PM2 was applied to the vulcanized fiber web at a weight of 105 gsm (drying down to about 86.3 gsm). The oven temperature was 121° C.
- Example 6 was prepared as in Example 5, except that PM2 was applied to the vulcanized fiber web at a weight of 62.4 gsm (drying down to about 51.8 gsm).
- Example 7 was prepared as in Example 5, except that PM2 was applied to the vulcanized fiber web at a weight of 20.8 gsm (drying down to about 17.3 gsm).
- Example 8 was prepared as in Example 1, except the weight of AR1 was 62.3 gsm (drying down to about 21.8 gsm).
- Example 9 was prepared as in Example 1, except the weight of AR1 was 37.4 gsm (drying down to about 13.1 gsm).
- Example 10 was prepared as in Example 1, except the weight of AR1 was 18.5 gsm (drying down to about 6.5 gsm).
- Example 11 was prepared as in Example 1, except that AR1 was applied to the same side of the vulcanized fiber web in three separate trips. The total add-on for the three trips was approximately 178 gsm (62.3 gsm dry). When abrasive discs were cut and flexed from this material, the backsize tended to flake off and no longer provided a uniform back side coating. These discs curled more severely than the untreated comparatives.
- Comparative Example B was prepared according to Example 1, with the exception that no backsize was applied to the backing.
- Comparative Examples C and D were ANSI grade 50 abrasive vulcanized fiber discs, 7 inches (18 cm) in diameter with a 7 ⁇ 8-inch (2.2 cm) center hole, obtained from Marvel Abrasives, Chicago, Ill., under the trade designation “50 GRIT CG CERAMIC RESIN BOND FREE DISC”) and Norton Company, Worcester, Mass., under the trade designation “50 GRIT F986 GREENLYTE PLUS”, respectively. The shape results, in mm, are recorded in Table IV (below).
- Example 10 Abrasive dics of Example 10 and Comparative Examples B and C were evaluated using the Grinding Test. Test results are reported in Table V (below). TABLE V FINAL AVER- HUMIDITY INI- AGE CON- TIAL FINAL TOTAL TOTAL DITION, CUT, CUT, CUT, EXAMPLE % RH DISC g g g g Comparative 20 1 88.7 25.4 985.6 902.9 Example B Comparative 20 2 91.3 14.7 854.3 Example B Comparative 20 3 88.2 18.1 868.8 Example B Example 10 20 1 91.0 26.9 1004.6 926.6 ′′ 20 2 90.1 20.0 891.5 ′′ 20 3 93.1 14.1 883.8 Comparative 20 1 73.3 13.9 712.6 650.3 Example C Comparative 20 2 72.0 15.5 588.0 Example C Comparative 60 1 79.8 17.7 864.1 841.8 Example B Comparative 60 2 84.0 13.4 824.8 Example B Comparative 60 3 81.7 16.3 875.5 Example B Comparative 60 4 8
- Example 12 was prepared using a 51-mm diameter disc cut from the abrasive disc according to Example 1. A nylon button was applied to the web according to the Spin Welding Procedure with machine settings as shown in Table VII.
- Example 13 was prepared and tested according to Example 12 with the exception that the abrasive disc was from Example 4.
- Example 14 was prepared and tested according to Example 12 with the exception that the abrasive disc was from Example 5.
- Comparative Example E was prepared and tested according to Example 12 with the exception that the abrasive disc was from Comparative Example A.
- Example 15 was prepared by applying via a 2-roll coater PM2 to one side of a 305 mm wide VF web. This backsize coating was allowed to dry for 3 minutes in an oven set at 116° C. to a dry add-on weight of about 8.8 gsm. The backsized web was inverted and the coating and drying steps repeated to produce a presize treated (i.e., presized) and backsize treated (i.e., backsized) web. The presized and backsized web was wound into a roll and allowed to condition 7 to 10 days in a 50% RH environment.
- presize treated i.e., presized
- backsize treated i.e., backsized
- An abrasive coating consisting of 188 gsm of a make coating (PM2), 799 gsm particle coating (AP2), and 448 gsm of a size coating (PM3) was applied to the conditioned, backsized and presized web and cured. Short pieces of cured abrasive web were wound into loose rolls and steamed for 1 hour at 65° C. 178 mm diameter discs with 22 mm center holes were cut from the moist webs using a punch press. The discs were then passed twice through a 2.5 cm (1.0-inch) bar flexor in orthogonal directions across the disc face.
- the flexed discs were stacked and banded between wooden flanges into a bale and then cured further for 24 hours at 100° C.
- the baled discs were finally allowed to condition for 5 days at 70% RH, 24° C., and then 5 more days in a 45% RH, 24° C. environment.
- Comparative Example F was prepared as Example 15 with the exception that both the backsize and presize coatings were omitted.
- Example 15 and Comparative Example F were tested according to Shape Measurement Procedure C and Grinding Test 2. The results are reported in Table VII (below). TABLE VII Height Change @ Humidity Condition Total 20% RH, 45% RH, 70% RH, Cut, HEIGHT, mm HEIGHT, mm HEIGHT, mm grams Example 15 5.12 1.40 29.65 1715.5 Comparative 5.50 2.96 35.55 1511.8 Example F
- Example 16 was prepared identically to Example 4 with the additional step of applying a presize (PM1, 38.9 gsm wet add-on (20.8 gsm dry add-on)) to the front side of the VF web by the same procedure as described for the backsize application in Example 4.
- a presize PM1, 38.9 gsm wet add-on (20.8 gsm dry add-on)
- Example 16 was tested according to Shape Measurement Procedure A.
- the Delta Height was 16.65 mm.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Polishing Bodies And Polishing Tools (AREA)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/136,692 US20060265967A1 (en) | 2005-05-24 | 2005-05-24 | Abrasive articles and methods of making and using the same |
EP06770713A EP1883500A1 (en) | 2005-05-24 | 2006-05-22 | Abrasive articles and methods of making and using the same |
PCT/US2006/019544 WO2006127502A1 (en) | 2005-05-24 | 2006-05-22 | Abrasive articles and methods of making and using the same |
CNA2006800177522A CN101180159A (zh) | 2005-05-24 | 2006-05-22 | 磨料制品及其制造方法和使用方法 |
JP2008513567A JP2008542043A (ja) | 2005-05-24 | 2006-05-22 | 研磨材物品とその作製方法及び使用方法 |
KR1020077027258A KR20080011300A (ko) | 2005-05-24 | 2006-05-22 | 연마 용품 및 이의 제조 및 이용 방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US11/136,692 US20060265967A1 (en) | 2005-05-24 | 2005-05-24 | Abrasive articles and methods of making and using the same |
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US20060265967A1 true US20060265967A1 (en) | 2006-11-30 |
Family
ID=36941632
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Application Number | Title | Priority Date | Filing Date |
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US11/136,692 Abandoned US20060265967A1 (en) | 2005-05-24 | 2005-05-24 | Abrasive articles and methods of making and using the same |
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US (1) | US20060265967A1 (ko) |
EP (1) | EP1883500A1 (ko) |
JP (1) | JP2008542043A (ko) |
KR (1) | KR20080011300A (ko) |
CN (1) | CN101180159A (ko) |
WO (1) | WO2006127502A1 (ko) |
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US20100203282A1 (en) * | 2007-08-13 | 2010-08-12 | Keipert Steven J | Coated abrasive laminate disc and methods of making the same |
CN104144769A (zh) * | 2012-03-16 | 2014-11-12 | 圣戈班磨料磨具有限公司 | 研磨制品和用于精修表面的方法 |
CN106239356A (zh) * | 2016-09-05 | 2016-12-21 | 咏巨科技有限公司 | 研磨垫修整方法、研磨垫修整装置及化学机械研磨设备 |
EP4084931A4 (en) * | 2019-12-31 | 2024-01-10 | Saint-gobain Abrasives, Inc | RIGID BACK LAYER TO PREVENT FIBER DISK WAVING |
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US20090325466A1 (en) * | 2008-06-30 | 2009-12-31 | 3M Innovative Properties Company | Coated abrasive articles and methods of making and using the same |
CN101829962B (zh) * | 2010-03-25 | 2011-09-14 | 湖北玉立砂带集团股份有限公司 | 一种金属复合板专用砂带及其制备方法 |
EP2640553B1 (en) * | 2010-11-18 | 2019-04-17 | 3M Innovative Properties Company | Convolute abrasive wheel and method of making the same |
CN105729316B (zh) * | 2016-02-25 | 2018-09-18 | 泉州众志新材料科技有限公司 | 一种人造石磨片 |
KR102245260B1 (ko) * | 2020-10-06 | 2021-04-26 | 에스케이씨솔믹스 주식회사 | 연마패드 및 이를 이용한 반도체 소자의 제조방법 |
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Also Published As
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WO2006127502A1 (en) | 2006-11-30 |
KR20080011300A (ko) | 2008-02-01 |
CN101180159A (zh) | 2008-05-14 |
JP2008542043A (ja) | 2008-11-27 |
EP1883500A1 (en) | 2008-02-06 |
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