EP2697416A2 - Article abrasif non tissé contenant des agglomérats liés à un élastomère de grain abrasif façonné - Google Patents

Article abrasif non tissé contenant des agglomérats liés à un élastomère de grain abrasif façonné

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Publication number
EP2697416A2
EP2697416A2 EP12771150.5A EP12771150A EP2697416A2 EP 2697416 A2 EP2697416 A2 EP 2697416A2 EP 12771150 A EP12771150 A EP 12771150A EP 2697416 A2 EP2697416 A2 EP 2697416A2
Authority
EP
European Patent Office
Prior art keywords
abrasive
nonwoven
agglomerates
particles
abrasive article
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
Application number
EP12771150.5A
Other languages
German (de)
English (en)
Other versions
EP2697416B1 (fr
EP2697416A4 (fr
Inventor
Bret W. Ludwig
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Innovative Properties Co
Original Assignee
3M Innovative Properties Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by 3M Innovative Properties Co filed Critical 3M Innovative Properties Co
Publication of EP2697416A2 publication Critical patent/EP2697416A2/fr
Publication of EP2697416A4 publication Critical patent/EP2697416A4/fr
Application granted granted Critical
Publication of EP2697416B1 publication Critical patent/EP2697416B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/413—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties containing granules other than absorbent substances
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions

Definitions

  • Nonwoven abrasive articles generally have a nonwoven web (e.g., a lofty open fibrous web), abrasive particles, and a binder material (commonly termed a "binder") that bonds the fibers within the nonwoven web to each other and secures the abrasive particles to the nonwoven web.
  • a binder material commonly termed a "binder”
  • nonwoven abrasive articles include nonwoven abrasive hand pads such as those marketed by 3M Company of Saint Paul, Minnesota under the trade designation "SCOTCH-BRITE".
  • nonwoven abrasive articles include convolute abrasive wheels and unitized abrasive wheels.
  • Nonwoven abrasive wheels typically have abrasive particles distributed through the layers of nonwoven web bonded together with a binder that bonds layers of nonwoven webs together, and likewise bonds the abrasive particles to the nonwoven web.
  • Unitized abrasive wheels have individual discs of nonwoven web arranged in a parallel fashion to form a cylinder having a hollow axial core.
  • convolute abrasive wheels have a nonwoven web that is spirally wound about and affixed to a core member.
  • nonwoven abrasive articles while using them on a work piece are import performance attributes. For some applications, reducing the resulting surface roughness (finish) on the work piece while maintaining or even increasing the cut of the nonwoven abrasive article in use is very desirable. It was surprisingly found that nonwoven abrasive articles according to the present invention exhibit significant improvements in the surface finish, as evaluated according to the test methods disclosed, when compared to alternative nonwoven abrasive articles as shown in the Examples.
  • the flexible bound agglomerates of formed abrasive particles produced a finer finish than nonwoven abrasive articles made using the identical formed abrasive particles that were not agglomerated.
  • agglomerating the formed abrasive particles would only increase the life of the abrasive article, and the resulting finish would be identical to non-agglomerated abrasive particles having the identical size.
  • the invention resides in a nonwoven abrasive article comprising a nonwoven web; agglomerates comprising formed ceramic abrasive particles bound together by a first flexible binder; and a second binder binding the agglomerates to the nonwoven fiber web.
  • FIG. 1 is a perspective view of an exemplary nonwoven abrasive article according to the present invention
  • FIG. 2 is a perspective schematic view of an exemplary convolute abrasive wheel according to one aspect of the present invention.
  • FIG. 3 is a perspective schematic view of an exemplary unitized abrasive wheel according to another aspect of the present invention.
  • FIG. 4 is a photomicrograph of one embodiment of an abrasive agglomerate made from formed abrasive particles.
  • FIG. 5 is a photomicrograph of another embodiment of an abrasive agglomerate made from formed abrasive particles.
  • FIG. 6 is a photomicrograph of another embodiment of an abrasive agglomerate made from formed abrasive particles.
  • cur means hardening a material, either by drying (i.e., evaporation of solvent), polymerizing (e.g., providing a sufficient degree of chain extension of the curable polyurethane prepolymer), or cooling a molten material.
  • the term "flexible binder” means that the cured binder material has a modulus of elasticity such that the cured binder material is able to bend a significant amount without breaking unlike a phenolic binder which would break.
  • the modulus of elasticity can be less than 28,000; or less than 25,000 or less than 23,000 psi as tested by ASTM D882.
  • suitable flexible binders include those of polyurethane, polyurea, polyisoprene, polybutadiene, polychloroprene, butyl rubber, styrene-butadiene copolymer, and nitrile rubber.
  • formed ceramic abrasive particle means an abrasive particle having at least a partially replicated shape.
  • Non-limiting processes to make formed abrasive particles include shaping the precursor ceramic abrasive particle in a mold having a predetermined shape to make shaped ceramic abrasive particles, extruding the precursor ceramic abrasive particle through an orifice having a predetermined shape, printing the precursor ceramic abrasive particle though an opening in a printing screen having a predetermined shape, or embossing the precursor ceramic abrasive particle into a predetermined shape or pattern.
  • Non-limiting examples of formed ceramic abrasive particles include shaped ceramic abrasive particles, such as triangular plates as disclosed in U.S.
  • the term "mineral” means abrasive particles or a mixture of abrasive particles and filler.
  • exemplary abrasive articles according to the present invention including lofty open nonwoven abrasive articles (e.g., webs and sheets), unitized abrasive wheels, and convolute abrasive wheels, may be manufactured through processes that include steps such as, for example, coating a curable composition, typically in slurry form, on a nonwoven web.
  • the curable composition comprises: a curable polyurethane prepolymer; an effective amount of an amine curative; at least one of a cationic surfactant, anionic surfactant, fluorinated nonionic surfactant, or silicone -based nonionic surfactant; and a dipodal aminosilane.
  • the nonwoven web is typically compressed (i.e., densified) relative to nonwoven webs used in lofty open nonwoven fiber articles.
  • Nonwoven webs suitable for use in the aforementioned abrasive articles are well known in the abrasives art.
  • the nonwoven web comprises an entangled web of fibers.
  • the fibers may comprise continuous fiber, staple fiber, or a combination thereof.
  • the nonwoven web may comprise staple fibers having a length of at least about 20 millimeters (mm), at least about 30 mm, or at least about 40 mm, and less than about 110 mm, less than about 85 mm, or less than about 65 mm, although shorter and longer fibers (e.g., continuous filaments) may also be useful.
  • the fibers may have a fineness or linear density of at least about 1.7 decitex (dtex, i.e., grams/10000 meters), at least about 6 dtex, or at least about 17 dtex, and less than about 560 dtex, less than about 280 dtex, or less than about 120 dtex, although fibers having lesser and/or greater linear densities may also be useful. Mixtures of fibers with differing linear densities may be useful, for example, to provide an abrasive article that upon use will result in a specifically preferred surface finish. If a spunbond nonwoven is used, the filaments may be of substantially larger diameter, for example, up to 2 mm or more in diameter.
  • the nonwoven web may be manufactured, for example, by conventional air laid, carded, stitch bonded, spun bonded, wet laid, and/or melt blown procedures.
  • Air laid nonwoven webs may be prepared using equipment such as, for example, that available under the trade designation "RANDO WEBBER" commercially available from Rando Machine Company of Ard, New York.
  • Nonwoven webs are typically selected to be suitably compatible with adhering binders and abrasive particles while also being processable in combination with other components of the article, and typically can withstand processing conditions (e.g., temperatures) such as those employed during application and curing of the curable composition.
  • the fibers may be chosen to affect properties of the abrasive article such as, for example, flexibility, elasticity, durability or longevity, abrasiveness, and finishing properties.
  • fibers that may be suitable include natural fibers, synthetic fibers, and mixtures of natural and/or synthetic fibers.
  • synthetic fibers include those made from polyester (e.g., polyethylene terephthalate), nylon (e.g., hexamethylene adipamide, polycaprolactam), polypropylene, acrylonitrile (i.e., acrylic), rayon, cellulose acetate, polyvinylidene chloride-vinyl chloride copolymers, and vinyl chloride- acrylonitrile copolymers.
  • suitable natural fibers include cotton, wool, jute, and hemp.
  • the fiber may be of virgin material or of recycled or waste material, for example, reclaimed from garment cuttings, carpet manufacturing, fiber manufacturing, or textile processing.
  • the fiber may be homogenous or a composite such as a bicomponent fiber (e.g., a co-spun sheath-core fiber).
  • the fibers may be tensilized and crimped, but may also be continuous filaments such as those formed by an extrusion process.
  • Combinations of fibers may also be used.
  • the nonwoven fiber web Prior to impregnation with the curable composition, the nonwoven fiber web typically has a weight per unit area (i.e., basis weight) of at least about 50 grams per square meter (gsm), at least about 100 gsm, or at least about 200 gsm; and/or less than about 400 gsm, less than about 350 gsm, or less than about 300 gsm, as measured prior to any coating (e.g., with the curable composition or optional pre-bond resin), although greater and lesser basis weights may also be used.
  • basis weight i.e., basis weight
  • the fiber web prior to impregnation with the curable composition, typically has a thickness of at least about 5 mm, at least about 6 mm, or at least about 10 mm; and/or less than about 200 mm, less than about 75 mm, or less than about 30 mm, although greater and lesser thicknesses may also be useful.
  • the prebond resin serves, for example, to help maintain the nonwoven web integrity during handling, and may also facilitate bonding of a urethane binder to the nonwoven web.
  • prebond resins include phenolic resins, urethane resins, hide glue, acrylic resins, urea-formaldehyde resins, melamine- formaldehyde resins, epoxy resins, and combinations thereof.
  • the amount of prebond resin used in this manner is typically adjusted toward the minimum amount consistent with bonding the fibers together at their points of crossing contact. If the nonwoven web includes thermally bondable fibers, thermal bonding of the nonwoven web may also be helpful to maintain web integrity during processing.
  • Useful abrasive particles for incorporating into the agglomerates of the invention are formed ceramic abrasive particles and, in particular, shaped ceramic abrasive particles.
  • Shaped ceramic abrasive particles were prepared according to the disclosures of copending U.S. Patent Publication 2010/0151196.
  • the shaped ceramic abrasive particles were prepared by shaping alumina sol gel from, for example, equilateral triangle-shaped polypropylene mold cavities of side length 0.054 inch (1.37 mm) and a mold depth of 0.012 inch (0.3 mm). After drying and firing, such resulting shaped ceramic abrasive particles comprised triangular plates that were about 570 micrometers (longest dimension) and would pass through a 30-mesh sieve.
  • inventive articles may also contain conventional (e.g., crushed) abrasive particles.
  • conventional abrasive particles for blending with the shaped ceramic abrasive particles include any abrasive particles known in the abrasive art.
  • 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 mixtures thereof.
  • the abrasive particles may be in the form of, for example, individual particles, agglomerates, composite particles, and mixtures thereof.
  • the conventional abrasive particles may, for example, have an average diameter of at least about 0.1 micrometer, at least about 1 micrometer, or at least about 10
  • the conventional abrasive particles may have an abrasives industry specified nominal grade.
  • abrasives industry accepted grading standards include those known as the American National Standards Institute, Inc. (ANSI) standards, Federation of European Producers of Abrasive Products (FEPA) standards, and Japanese Industrial Standard (JIS) standards.
  • Exemplary ANSI grade designations include: ANSI 4, ANSI 6, ANSI 8, ANSI 16, ANSI 24, ANSI 36, ANSI 40, ANSI 50, ANSI 60, ANSI 80, ANSI 100, ANSI 120, ANSI 150, ANSI 180, ANSI 220, ANSI 240, ANSI 280, ANSI 320, ANSI 360, ANSI 400, and ANSI 600.
  • Exemplary FEPA grade designations include P8, P12, P16, P24, P36, P40, P50, P60, P80, P100, P120, P150, P180, P220, P320, P400, P500, 600, P800, P1000, and P1200.
  • Exemplary JIS grade designations include HS8, JIS12, JIS16, JIS24, JIS36, JIS46, JIS54, JIS60, JIS80, JIS100, JIS 150, JIS 180, JIS220, JIS 240, JIS280, JIS320, JIS360, JIS400, JIS400, JIS600, JIS800, JIS 1000, JIS 1500, JIS2500, JIS4000, JIS6000, JIS8000, and JIS 10000.
  • the inventive agglomerates comprise a first flexible binder.
  • suitable flexible binders include those of polyurethane, polyurea, polyisoprene, polybutadiene, polychloroprene, butyl rubber, styrene-butadiene copolymer, and nitrile rubber.
  • a typical flexible binder for preparation of agglomerates comprising formed ceramic abrasive particles is a polyurethane binder.
  • useful urethane prepolymers include polyisocyanates and blocked versions thereof.
  • blocked polyisocyanates are substantially unreactive to isocyanate reactive compounds (e.g., amines, alcohols, thiols, etc.) under ambient conditions (e.g., temperatures in a range of from about 20 °C to about 25 °C), but upon application of sufficient thermal energy the blocking agent is released, thereby generating isocyanate functionality that reacts with the amine curative to form a covalent bond.
  • Useful polyisocyanates include, for example, aliphatic polyisocyanates (e.g., hexamethylene diisocyanate or trimethylhexamethylene diisocyanate); alicyclic polyisocyanates (e.g., hydrogenated xylylene diisocyanate or isophorone diisocyanate); aromatic polyisocyanates (e.g., tolylene diisocyanate or 4,4'-diphenylmethane
  • aliphatic polyisocyanates e.g., hexamethylene diisocyanate or trimethylhexamethylene diisocyanate
  • alicyclic polyisocyanates e.g., hydrogenated xylylene diisocyanate or isophorone diisocyanate
  • aromatic polyisocyanates e.g., tolylene diisocyanate or 4,4'-diphenylmethane
  • diisocyanate diisocyanate
  • adducts of any of the foregoing polyisocyanates with a polyhydric alcohol e.g., a diol, low molecular weight hydroxyl group-containing polyester resin, water, etc.
  • adducts of the foregoing polyisocyanates e.g., isocyanurates, biurets
  • mixtures thereof e.g., isocyanurates, biurets
  • Useful commercially available polyisocyanates include, for example, those available under the trade designation "ADIPRENE” from Chemtura Corporation,
  • AIRTHANE and "VERSATHANE” from Air Products and Chemicals, Allentown, Pennsylvania (e.g., "AIRTHANE APC-504", “AIRTHANE PST-95A”, “AIRTHANE PST-85A”, “AIRTHANE PET-91A”, “AIRTHANE PET-75D”, “VERSATHANE STE- 95A”, “VERSATHANE STE-P95”, “VERSATHANE STS-55”, “VERSATHANE SME- 90A”, and “VERSATHANE MS-90A”).
  • polyisocyanates such as, for example, those mentioned above may be blocked with a blocking agent according to various techniques known in the art.
  • blocking agents include ketoximes (e.g., 2-butanone oxime); lactams (e.g., epsilon-caprolactam); malonic esters (e.g., dimethyl malonate and diethyl malonate); pyrazoles (e.g., 3,5-dimethylpyrazole); alcohols including tertiary alcohols (e.g., t-butanol or 2,2-dimethylpentanol), phenols (e.g., alkylated phenols), and mixtures of alcohols as described.
  • ketoximes e.g., 2-butanone oxime
  • lactams e.g., epsilon-caprolactam
  • malonic esters e.g., dimethyl malonate and diethyl malonate
  • pyrazoles
  • Exemplary useful commercially-available blocked polyisocyanates include those marketed by Chemtura Corporation under the trade designations "ADIPRENE BL 11", “ADIPRENE BL 16", “ADIPRENE BL 31”, and blocked polyisocyanates marketed by Baxenden Chemicals, Ltd., Accrington, England under the trade designation “TRIXENE” (e.g., "TRIXENE BL 7641", “TRIXENE BL 7642”, “TRIXENE BL 7772", and
  • the amount of urethane prepolymer present in the curable composition is in an amount of from 10 to 40 percent by weight, more typically in an amount of from 15 to 30 percent by weight, and even more typically in an amount of from 20 to 25 percent by weight based on the total weight of the curable composition, although amounts outside of these ranges may also be used.
  • Suitable amine curatives include aromatic, alkyl-aromatic, or alkyl polyfunctional amines, preferably primary amines.
  • useful amine curatives include 4,4'- methylenedianiline; polymeric methylene dianilines having a functionality of 2.1 to 4.0 which include those known under the trade designations "CURITHANE 103",
  • the amine curative should be present in an amount effective (i.e., an effective amount) to cure the blocked polyisocyanate to the degree required by the intended application; for example, the amine curative may be present in a stoichiometric ratio of curative to isocyanate (or blocked isocyanate) in a range of from 0.8 to 1.35; for example, in a range of from 0.85 to 1.20, or in a range of from 0.90 to 0.95, although stoichiometric ratios outside these ranges may also be used.
  • the curable composition will include at least one organic solvent (e.g., isopropyl alcohol or methyl ethyl ketone) to facilitate coating of the curable composition on the nonwoven fiber web, although this is not a requirement.
  • the curable composition may be mixed with and/or include one or more additives.
  • additives include fillers, plasticizers, surfactants, lubricants, colorants (e.g., pigments), bactericides, fungicides, grinding aids, and antistatic agents.
  • the curable composition (including any solvent that may be present) is coated onto the nonwoven fiber web in an amount of from 1120 to 2080 gsm, more typically 1280 - 1920 gsm, and even more typically 1440 - 1760 gsm, although values outside these ranges may also be used.
  • Filler materials other than conventional abrasive particles may be blended with shaped ceramic abrasive particles in the inventive agglomerates.
  • useful fillers for this invention include metal carbonates (such as calcium carbonate, calcium magnesium carbonate, sodium carbonate, magnesium carbonate), silica (such as quartz, glass beads, glass bubbles and glass fibers), silicates (such as talc, clays, montmorillonite, feldspar, mica, calcium silicate, calcium metasilicate, sodium aluminosilicate, sodium silicate), metal sulfates (such as calcium sulfate, barium sulfate, sodium sulfate, aluminum sodium sulfate, aluminum sulfate), gypsum, vermiculite, sugar, wood flour, aluminum trihydrate, carbon black, metal oxides (such as calcium oxide, aluminum oxide, tin oxide, titanium dioxide), metal sulfites (such as calcium sulfite), thermoplastic particles (such as polycarbonate, polyetherimide,
  • the filler may also be a salt such as a halide salt.
  • halide salts include sodium chloride, potassium cryolite, sodium cryolite, ammonium cryolite, potassium tetrafluoroborate, sodium tetraf uoroborate, silicon fluorides, potassium chloride, magnesium chloride.
  • metal fillers include, tin, lead, bismuth, cobalt, antimony, cadmium, iron and titanium.
  • Other miscellaneous fillers include sulfur, organic sulfur compounds, graphite, lithium stearate and metallic sulfides.
  • the size of the agglomerates have a maximum diameter (if generally spherical) or a maximum side edge length (if generally cylindrical, ovoid, or other geometric shape) ranging from 0.8 mm to 5 mm, or 1.4 mm to 4 mm, or 1.8 to 3 mm and may be spherical, ovoid, cylindrical, pyramidal, conical or any multi-sided Platonic solid (tetrahedron, octahedron, etc.).
  • the ratio of the formed abrasive particle size (measuring the edge length of the formed abrasive particles) divided by the agglomerate size (measuring the maximum diameter or maximum side edge length of the agglomerate) is 0.0033 to 0.5 (approximately 300 to 2 formed abrasive particles across the agglomerate), or 0.01 to 0.33 (approximately 100 to 3 formed abrasive particles across the agglomerate), or 0.05 to 0.25 (approximately 20 to 4 formed abrasive particles across the agglomerate).
  • filler particles conventional crushed abrasive particles or diluents
  • they have an average particle size less than that of the formed ceramic abrasive particles, or the ratio of the filler particle size (maximum diameter) divided by the formed abrasive particles size (measuring the maximum diameter or maximum side edge length of the agglomerate) is 0.001 to 1.0, or 0.003 to 0.5, or 0.01 to 0.1.
  • Typical inventive agglomerates can comprise no more than 30 weight percent (wt. %) first fiexible binder, no more than 20 wt. % first fiexible binder, no more than 15 wt. % first flexible binder, or even no more than 10 wt. % first flexible binder.
  • Typical inventive % first fiexible binder no more than 20 wt. % first fiexible binder, no more than 15 wt. % first flexible binder, or even no more than 10 wt. % first flexible binder.
  • agglomerates comprise at least 50 wt. % formed ceramic abrasive particles.
  • the formed ceramic abrasive particle content is 50 wt. % to 98 wt. %, 75 wt. % to 96 wt. %, or 80 wt. % to 94 wt. %;
  • the resin content is 2 wt. % to 20 wt. %, 4 wt. % to 10 wt. %, or 5 wt. % to 8 wt. %;
  • the filler particle content is 0 wt. % to 40 wt. %, 10 wt. % to 35 wt. %, or 15 wt. % to 30 wt. %. It is understood the above ranges for the various properties can be combined or selected in any manner to specify the agglomerate's attributes.
  • the nonwoven abrasive web is prepared by adhering the agglomerates of the invention to a nonwoven web with a curable second binder.
  • the coating weight for the abrasive agglomerates (independent of other ingredients in the curable
  • the coating weight of the abrasive agglomerates on the nonwoven web may be at least 200 grams per square meter (g/m), at least 600 g/m, or at least 800 g/m; and/or less than 2000 g/m, less than about 1600 g/m, or less than about 1200 g/m, although greater or lesser coating weights may be also be used.
  • Second binders useful for adhering the agglomerates to the nonwoven fiber web are known in the art and are selected according to the final product requirements.
  • Typical binders include those comprising polyurethane, phenolic, acrylate, and blends of phenolic and acrylate.
  • Useful polyurethane binder materials and their precursors for adhering agglomerates to nonwoven web have been described herein above.
  • Phenolic materials are useful binder precursors because of their thermal properties, availability, cost, and ease of handling.
  • Resole phenolics have a molar ratio of
  • Emulsions of crosslinked acrylic resin particles may also find utility in the present invention.
  • Some binder precursors include a phenolic mixed with a latex.
  • latexes include materials containing acrylonitrile butadiene, acrylics, butadiene, butadiene - styrene, and combinations thereof.
  • These latexes are commercially available from a variety of different sources and include those available under the trade designations RHOPLEX and ACRYLSOL commercially available from Rohm and Haas Company, FLEXCRYL and VALTAC commercially available from Air Products & Chemicals Inc., SYNTHEMUL, TYCRYL, and TYLAC commercially available from Reichold Chemical Co., HYCAR and GOODRITE commercially available from B. F. Goodrich,
  • CHEMIGUM commercially available from Goodyear Tire and Rubber Co.
  • NEOCRYL commercially available from ICI
  • BUTAFON commercially available from BASF
  • RES commercially available from Union Carbide.
  • Nonwoven abrasive articles of the invention may take any of a variety of conventional forms.
  • FIG. 1 shows a nonwoven abrasive article 100 comprising a nonwoven web; agglomerates comprising formed ceramic abrasive particles bound together by a first flexible binder; and a second binder binding the agglomerates to the nonwoven fiber web.
  • FIGS. 4-6 show abrasive agglomerates comprising shaped ceramic abrasive particles and a first flexible binder.
  • the shaped ceramic abrasive particles comprises triangular plates as seen.
  • Nonwoven abrasive articles are in the form of wheels.
  • Nonwoven abrasive wheels are typically in the form of a disc or right cylinder having dimensions that may be very small, e.g., a cylinder height on the order of a few millimeters or very large, e.g., a meter or more, and a diameter which may be very small, e.g., on the order of a few centimeters, or very large, e.g., tens of centimeters.
  • Wheels typically have a central opening for support by an appropriate arbor or other mechanical holding means to enable the wheels to be rotated in use. Wheel dimensions, configurations, means of support, and means of rotation are all well known in the art.
  • Convolute abrasive wheels may be provided, for example, by winding the nonwoven web that has been impregnated with the curable composition under tension around a core member (e.g., a tubular or rod-shaped core member) such that the impregnated nonwoven layers become compressed, and then curing the curable composition to provide, in one embodiment, a polyurethane binder binding the abrasive agglomerates to the layered nonwoven web and binding layers of the layered nonwoven web to each other.
  • a core member e.g., a tubular or rod-shaped core member
  • layered nonwoven fiber web 210 coated with binder binding the abrasive agglomerates to the layered nonwoven fiber web and binding layers of the layered nonwoven fiber web to each other is spirally disposed around and affixed to core member 230.
  • convolute abrasive wheels may be dressed prior to use to remove surface irregularities, for example, using methods known in the abrasive arts.
  • An exemplary unitized abrasive wheel is shown in FIG. 3, and can be provided, for example, by layering the impregnated above-provided nonwoven web 310 (e.g., as a layered continuous web or as a stack of sheets) compressing the nonwoven layers, curing the curable composition (e.g., using heat), and die cutting the resultant abrasive article to provide a unitized abrasive wheel having a hollow axial core 320.
  • the layers are typically compressed to form a bun having a density that is from 1 to 20 times that of the density of the layers in their non- compressed state.
  • the bun is then typically subjected to heat molding (e.g., for from 2 to 20 hours) at elevated temperature (e.g., at 135 °C), typically depending on the urethane prepolymer and bun size.
  • Initiator S Two weight percent solution of 1 , 1 '- Azobis(cyclohexanecarbonitrile) in methanol
  • SAP1 Shaped ceramic abrasive particles of about 570 micrometers
  • SAP2 Shaped ceramic abrasive particles of about 550 micrometers
  • Agglomerated binder solutions for the Examples were prepared by mixing components as described below.
  • Binder AR1 was 72.3% BL16, 26.8% K-450S, and 0.9% D-1122.
  • Binder AR2 was 63.9% Phenolic, 27.7% tap water, 7.8% SR511, and 0.6% D- 1122.
  • Binder AR3 was 87% of a free radical-cured resin selected from Acrylic 1 through Acrylic7, inclusive, and 13%> Initiator S.
  • Binder AR4 was 61.4% BL16, 22.7% K4-450S, 15.3% PMA, and 0.6% D-1122.
  • Agglomerate precursor compositions included mineral (abrasive particles with optional fillers) and binder mixed by hand with a spatula.
  • Agglomerates prepared with AR1, AR2, and AR4 were 94 wt. % mineral based on solids content.
  • Agglomerates prepared with AR3 were 90 wt. % mineral based on solids content.
  • composition into the cavities of 15 cm by 86 cm sheets of microreplicated polypropylene tooling had total thickness of 2.2 mm, a plurality of precisely-shaped, microreplicated cavities 4.0 mm square and 1.6 mm deep separated by walls 1.5 mm thick.
  • the tooling was prepared from a corresponding master roll generally according to the procedure of U.S. Pat. No. 6,076,248 to Hoopman et al.
  • Filled sheets of polypropylene tooling were heated in a forced air oven to cure the agglomerates.
  • Urethane agglomerates were cured for 20 minutes at 260 °F (127 °C).
  • Phenolic agglomerates were cured at 200 °F (91 °C) for 90 minutes followed by 16 hours at 215 °F (102 °C).
  • Agglomerates containing free radical cured resins were cured for 30 minutes at 280°F (138 °C).
  • the cured agglomerates were removed from the tooling by ultrasonic energy. More particularly, the backside of the tooling was pulled, under tension, across the forward edge of an ultrasonic horn tapered to a single edge.
  • the horn was oscillated at a frequency of 19,100 HZ at amplitude of about 130 micrometers.
  • the horn was composed of 6-4 titanium and was driven with a 900 watt 184 V Branson power source coupled with a 2: 1 Booster 802 piezoelectric converter. Examples of the resulting abrasive agglomerates are shown in FIG. 4.
  • abrasive particles 3000 grams was thoroughly mixed with 250 grams of AR1 producing a friable, tacky agglomerate precursor composition.
  • the agglomerate precursor composition was processed into abrasive agglomerate particles with the aid of a size reduction machine obtained under the trade designation "QUADRO COMIL" ("Model #197", Quadro Engineering Incorporated, Waterloo, Ontario, Canada). Details of the operation of the size reduction machine can be found in WO 02/32832 Al to Culler et.al.
  • the premix was forced through the 75 mil (1.9 mm) circular openings of a conical screen using an impeller driven at a range of 50 rpm to 3500 rpm.
  • the filamentary shaped agglomerate precursor particle separates and falls by gravity to an aluminum collection pan.
  • a mono- or bi-layer of precursor particles were collected in a pan, which was then placed in an oven set to 320 °F (160 °C) for 15 minutes in order to cure the binder resin.
  • the abrasive agglomerate particles were size-reduced by running them once through the size reduction machine ("QUADRO COMIL") set up with a conical screen pierced by 95 mil (2.4 mm) round holes. The size-reduced particles were sieved on a 14-mesh (1400 micron) screen. Those particles retained on the screen were used to produce unitized abrasive wheels.
  • FIG. 5 An example of the abrasive agglomerate is shown in FIG. 5.
  • Agglomerates of abrasive grain, or abrasive grain and fillers were produced by applying drops of AR4 to beds of mineral one to two centimeters in thickness. Drops were produced by feeding the solution through a blunt-tipped 22-guage hypodermic needle supported in a vertical position approximately seven centimeters above the mineral bed. The resin droplets wicked into the mineral beds within 10 seconds of application, wetting a volume of material dependent upon the surface area of the mineral or mineral/filler blends. The agglomerates were cured at 302°F (150 °C) for 30 minutes and then sieved from the non-agglomerated mineral, which was recycled back into the agglomerate forming process.
  • AR2 was dripped onto the mineral or mineral/filler bed in a similar manner and cured at 200 °F (91 °C) for 90 minutes followed by 16 hours at 215 °F (102 °C).
  • Individual agglomerates weighed between 0.033 and 0.076 grams and contained from twelve to four percent resin by weight.
  • An example of the resulting abrasive agglomerate is show in FIG. 6.
  • a nonwoven web was formed on an air laid fiber web forming machine, available under the trade designation "RANDO-WEBBER” from the Rando Machine Corporation of Ard, New York.
  • the fiber web was formed from 70 denier nylon crimp set fiber with a staple length of one and one -half inches (available from E. I. du Pont de Nemours & Company, Wilmington, Delaware).
  • the weight of the web was approximately 105 grams per square meter (gsm), and the thickness was approximately 0.4 inches (10 mm).
  • the web was conveyed to a horizontal, two-roll coater, where a pre-bond resin was applied at a wet add-on weight of 89 gsm.
  • the pre-bond resin had the following composition (all percentages relative to component weight): 54.1% BL16, 19.9% K450S, 26% PMA.
  • the pre-bond resin was cured to a non-tacky condition by passing the coated web through a convection oven at 330 °F (166 °C) for 4.5 minutes, yielding a pre-bonded, nonwoven web of approximately 6 mm thickness and having a basis weight of 168 gsm.
  • Unitized abrasive wheels were prepared from the pre-bonded nonwoven web as follows. A 9-inch (23-cm) square section was cut from the prebonded nonwoven web and saturated with one of two wheel adhesives. Wheel adhesive one (WA1) was 44% BL16, 16.4% K-450S, 15.8% PMA, 7% MP-22VF, 6% phenoxy, 9.9% kaolin, and 0.4% D-l 122. Wheel adhesive two (WA2) was 60.8% Phenolic, 31.2% water, 7.4% SR511, and 0.6% D- 1122.
  • Wheel adhesive one was 44% BL16, 16.4% K-450S, 15.8% PMA, 7% MP-22VF, 6% phenoxy, 9.9% kaolin, and 0.4% D-l 122.
  • Wheel adhesive two (WA2) was 60.8% Phenolic, 31.2% water, 7.4% SR511, and 0.6% D- 1122.
  • the saturated prebonded web was then passed through the nip of a roll coater having 4-inch (10-cm) diameter rubber rolls of 85-Shore A durometer hardness to remove excess resin until the desired resin add-on weight of 0.49 ⁇ 0.035 oz (14 ⁇ 1 g) for WA1 or 0.60 ⁇ 0.035 oz (17 ⁇ 1 g) for WA2 was obtained.
  • a roll coater having 4-inch (10-cm) diameter rubber rolls of 85-Shore A durometer hardness to remove excess resin until the desired resin add-on weight of 0.49 ⁇ 0.035 oz (14 ⁇ 1 g) for WA1 or 0.60 ⁇ 0.035 oz (17 ⁇ 1 g) for WA2 was obtained.
  • multiple passes through the nip at 11 fpm (3.35 mpm) under pressures of 10-21 psi (69-145 kPa) were required to reach the target weight.
  • seven sections of pre-bonded web were coated in the above manner.
  • the coated sections of prebonded web were placed in a forced air oven set at 260 °F (127 °C) for one minute to remove a majority of the solvent.
  • six sections of prebond were each covered with 42 grams of randomly, uniformly distributed mineral or mineral
  • agglomerates The six coated sections were then stacked and covered with a seventh section of prebond. A release liner was then applied to the top and bottom of the stack before it was placed in a hydraulic, heated platen press. A pressure of 5,000 psi (34.5 MPa) was applied to the platens. Consistent thickness of the unitized slab was maintained by placing 0.25 inch (0.635 cm) thick metal spacers in each corner of the platen. Stacks containing WA1 (urethane) were left in the press, set at 260 °F (127 °C), for 30 minutes. Stacks containing WA2 (phenolic) were left in the press, set at 200 °F (93 °C), for five hours.
  • WA1 urethane
  • WA2 phenolic
  • the press When the press was opened, the sections of web had fused together into a single, unitized slab.
  • the slab was then placed in a forced air oven set at 260 °F (127 °C) for two hours (WA1), or at 215 °F (102 °C) for 16 hours (WA2). After removal from the oven, the slab was cooled to room temperature, and an 8.0-inch (20-cm) diameter unitized abrasive wheel with a 1.25-inch (3.2-cm) center hole was die cut from it using a SAMCO SB-25 swing beam press manufactured by Deutsche vernier Schuhmaschinen GmbH & Co., Frankfurt, Germany.
  • a pre-weighed, 0.25 inch (6.4 mm)-thick unitized abrasive wheel to be tested was mounted in a vertical orientation on the arbor of a mechanically driven, variable speed lathe adjusted to generate a surface speed at the wheel's edge of approximately 3500 feet (1065 meters) per minute.
  • the edge of a 0.0625 inch (1.59 mm)-thick, two-inch by eleven-inch (5.08-cm by 27.9-cm) cold rolled carbon steel or T304 stainless steel panel held horizontally at the height of the arbor was plunged into the rotating edge of the wheel with approximately 5 pounds (22.2 Newtons) of force for 20 seconds.
  • the amount of material removed from the panel during the test sequence was designated as the "cut” and was defined as the difference between the weight of the panel before and after the test sequence.
  • the amount of material removed from the wheel during the test sequence was designated as the “wear” and was defined as the difference between the weight of the wheel before and after the test sequence.
  • Finish samples were produced by placing the 6.4 mm-thick wheels on a back stand and adjusting the speed to produce a surface speed of approximately 3500 feet (1065 meters) per minute.
  • the faces of 0.0625 inch (1.59 mm)-thick, two-inch by eleven-inch (5.08-cm by 27.94-cm) cold rolled carbon steel or T304 stainless steel panels were abraded while applying roughly five pounds (22.2 Newtons) of pressure.
  • a 4-inch (10.2- cm) length of panel was finished by passing the panel over the wheel eight times, stepping roughly 0.25 inch (6.4 mm) between passes and moving the panel approximately 2 inches (5.04 cm) per second. Finish was measured using a Perthometer PRK profilometer (Feinpruf GmbH; Gottingen, Germany). Ten measurements were taken on each surface. The high and low values were discarded and the remaining eight data points averaged.
  • Films for modulus measurements were prepared by placing 16 grams of AR1 on a circular stainless steel form with a diameter of 5.5 inches (14 cm) and a side wall 0.12 inch (3 mm) high. Samples were placed in a forced air oven set at 180 °F (82 °C) for one hour to drive off the majority of solvent. The oven was then set at 260 °F (127 °C) for two hours to complete curing. The resulting films, approximately 0.027 in (0.69 mm) thick, were removed from the steel form.
  • Urethane-bound unitized abrasive wheels were prepared according to the procedures set forth above in the sections on Preparation of Agglomerates and Unitized Abrasive Wheel Preparation, using the components reported in Table 1.
  • the unitized abrasive wheels were tested according to the Unitized Abrasive Wheel Performance Test and Unitized Abrasive Wheel Finish Testing. Results are reported in Table 2.
  • Comparative Examples G through L the cut and wear data were not collected because the smaller abrasive particle size resulted in very low cut. Comparative Examples G through L are presented to show the comparative finishes obtained.
  • Phenolic-bound unitized abrasive wheels were prepared according to the procedures set forth above in the sections Preparation of Agglomerates and Unitized Abrasive Wheel Preparation, using the ingredients reported in Table 3. The unitized abrasive wheels were tested according to the Unitized Abrasive Wheel Performance Test and Unitized Abrasive Wheel Finish Testing. Results are reported in Table 4.
  • the modulus of AR1 was measured according to the procedure in the section on Measurement of Resin Modulus above.
  • Urethane bound unitized wheels containing agglomerates bound by a variety of free radical cured resins were produced according to the procedures set forth above in the sections Preparation of Agglomerates and Unitized Abrasive Wheel Preparation, using the ingredients reported in Table 5.
  • the unitized abrasive wheels were tested according to the Unitized Abrasive Wheel Finish Testing. Results are reported in Table 6. The results show the data demonstrates that for the purposes of defining an agglomerate binder resin as 'flexible' or 'rigid' the transition occurs when the modulus value decreases to less than 30,000 psi as measured by ASTM D882.
  • Examples 8 and 9 and examples Z and AA were prepared to demonstrate the effect of filler on the finish produced by agglomerates of precisely shaped grain.
  • Urethane bound unitized abrasive wheels were prepared according to the procedures set forth above in the sections Preparation of Agglomerates and Unitized Abrasive Wheel Preparation, using the ingredients reported in Table 7.
  • the unitized abrasive wheels were tested according to the Unitized Abrasive Wheel Performance Test and Unitized Abrasive Wheel Finish Testing. Results are reported in Table 8. The results show the addition of fillers (particles other than formed ceramic abrasive particles) in the flexible binder agglomerates of formed ceramic abrasive particles results in a finer finish.
  • Examples 10 and 1 l were prepared to demonstrate that the unexpected improved finish result is independent of the method of agglomerate production.
  • Urethane bound unitized abrasive wheels were prepared according to the procedures set forth above in the sections Preparation of Agglomerates and Unitized Abrasive Wheel Preparation, using the variables reported in Table 9. The unitized abrasive wheels were tested according to the Unitized Abrasive Wheel Performance Test and Unitized Abrasive Wheel Finish Testing. Results are reported in Table 10.
  • agglomerating shaped ceramic abrasive particles with flexible resins is independent of the agglomerate's shape.
  • Examples 1-7 and comparatives A-Y were molded squares.
  • Examples 10 &11 were random shapes.

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Abstract

L'invention concerne un article abrasif non tissé formé à partir d'une bande non tissée et d'agglomérats comprenant des particules abrasives céramiques façonnées liées ensemble par un premier liant flexible et un second liant qui lie les agglomérats à la bande de fibres non tissées.
EP12771150.5A 2011-04-14 2012-03-29 Article abrasif non tissé contenant des agglomérats liés à un élastomère de grain abrasif façonné Active EP2697416B1 (fr)

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WO2012141905A3 (fr) 2012-12-27
CN103476979B (zh) 2016-01-06
BR112013026334A2 (pt) 2016-12-27
KR20140024884A (ko) 2014-03-03
CN103476979A (zh) 2013-12-25
JP2014514173A (ja) 2014-06-19
EP2697416B1 (fr) 2017-05-10
EP2697416A4 (fr) 2014-10-01
JP6000333B2 (ja) 2016-09-28
US20140080393A1 (en) 2014-03-20
PL2697416T3 (pl) 2017-09-29
ES2633316T3 (es) 2017-09-20
RU2013145788A (ru) 2015-05-20
WO2012141905A2 (fr) 2012-10-18

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