WO2013039688A1 - Method of refurbishing vinyl composition tile - Google Patents
Method of refurbishing vinyl composition tile Download PDFInfo
- Publication number
- WO2013039688A1 WO2013039688A1 PCT/US2012/052660 US2012052660W WO2013039688A1 WO 2013039688 A1 WO2013039688 A1 WO 2013039688A1 US 2012052660 W US2012052660 W US 2012052660W WO 2013039688 A1 WO2013039688 A1 WO 2013039688A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- abrasive
- floor
- particle size
- average particle
- structured
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 110
- 229920002554 vinyl polymer Polymers 0.000 title claims abstract description 49
- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title claims abstract description 36
- 239000002245 particle Substances 0.000 claims abstract description 149
- 239000002131 composite material Substances 0.000 claims abstract description 86
- 239000011230 binding agent Substances 0.000 claims abstract description 54
- 238000009408 flooring Methods 0.000 claims abstract description 17
- 230000003746 surface roughness Effects 0.000 claims description 32
- 239000006260 foam Substances 0.000 claims description 21
- 239000000835 fiber Substances 0.000 claims description 19
- 230000007423 decrease Effects 0.000 claims description 16
- 230000000717 retained effect Effects 0.000 claims description 4
- 230000003247 decreasing effect Effects 0.000 abstract description 3
- 239000010432 diamond Substances 0.000 description 71
- 229910003460 diamond Inorganic materials 0.000 description 62
- 239000010410 layer Substances 0.000 description 19
- 238000005498 polishing Methods 0.000 description 17
- 239000011521 glass Substances 0.000 description 15
- 230000001012 protector Effects 0.000 description 15
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 230000008569 process Effects 0.000 description 13
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 13
- 239000002243 precursor Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 10
- 238000005259 measurement Methods 0.000 description 10
- 238000000576 coating method Methods 0.000 description 9
- -1 for example Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
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- 239000011159 matrix material Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 230000003068 static effect Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 239000010425 asbestos Substances 0.000 description 5
- 238000012423 maintenance Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 5
- 229910052895 riebeckite Inorganic materials 0.000 description 5
- 239000004744 fabric Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920000515 polycarbonate Polymers 0.000 description 4
- 239000004417 polycarbonate Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 239000010426 asphalt Substances 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
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- 235000013824 polyphenols Nutrition 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052582 BN Inorganic materials 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000002241 glass-ceramic Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- VHKQAUGSGQUCDU-UHFFFAOYSA-N (6'-methoxy-3-oxospiro[2-benzofuran-1,9'-xanthene]-3'-yl) 2-(pyridin-2-yldisulfanyl)benzoate Chemical compound C=1C(OC)=CC=C(C2(C3=CC=CC=C3C(=O)O2)C2=CC=3)C=1OC2=CC=3OC(=O)C1=CC=CC=C1SSC1=CC=CC=N1 VHKQAUGSGQUCDU-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 240000004246 Agave americana Species 0.000 description 1
- 244000198134 Agave sisalana Species 0.000 description 1
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 244000260524 Chrysanthemum balsamita Species 0.000 description 1
- 235000005633 Chrysanthemum balsamita Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 240000008790 Musa x paradisiaca Species 0.000 description 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 241000220010 Rhode Species 0.000 description 1
- 101100033275 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) RCN2 gene Proteins 0.000 description 1
- 101100210368 Schizosaccharomyces pombe (strain 972 / ATCC 24843) wsp1 gene Proteins 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical class C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- MSYLJRIXVZCQHW-UHFFFAOYSA-N formaldehyde;6-phenyl-1,3,5-triazine-2,4-diamine Chemical class O=C.NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 MSYLJRIXVZCQHW-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 239000002223 garnet Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000005641 methacryl group Chemical group 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical class O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000004439 roughness measurement Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
- A47L11/00—Machines for cleaning floors, carpets, furniture, walls, or wall coverings
- A47L11/40—Parts or details of machines not provided for in groups A47L11/02 - A47L11/38, or not restricted to one of these groups, e.g. handles, arrangements of switches, skirts, buffers, levers
- A47L11/4036—Parts or details of the surface treating tools
- A47L11/4038—Disk shaped surface treating tools
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B1/00—Processes of grinding or polishing; Use of auxiliary equipment in connection with such processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B7/00—Machines or devices designed for grinding plane surfaces on work, including polishing plane glass surfaces; Accessories therefor
- B24B7/10—Single-purpose machines or devices
- B24B7/18—Single-purpose machines or devices for grinding floorings, walls, ceilings or the like
- B24B7/186—Single-purpose machines or devices for grinding floorings, walls, ceilings or the like with disc-type tools
-
- 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
- B24D13/00—Wheels having flexibly-acting working parts, e.g. buffing wheels; Mountings therefor
- B24D13/14—Wheels having flexibly-acting working parts, e.g. buffing wheels; Mountings therefor acting by the front face
Definitions
- the present disclosure broadly relates to methods for vinyl composition tile maintenance and repair.
- Vinyl composition tile is widely used as flooring in commercial and institutional settings such as, for example, grocery and other retail stores, schools, hospitals, light industrial applications (e.g., laboratories), and restaurants.
- vinyl tile There are two types of vinyl tile.
- the first, vinyl asbestos tile is comparable to asphalt tile, except that vinyl type resins are the binder instead of asphalt or other resins.
- vinyl type resins are the binder instead of asphalt or other resins.
- asbestos, pigments and inert fillers are used.
- Composition tile (VC tile). It is more porous than vinyl asbestos tile, and therefore more difficult to build initial gloss. Because of the relatively high filler content, these floors are only available in tile form.
- the recommended maintenance of VC tile floors generally involves aqueous polymer emulsion coatings and aqueous cleaners and strippers.
- VC tile is generally composed of binder, fillers and pigments compounded with additives such as, for example, stabilizers and processing aides.
- the binder consists of polymers and/or copolymers of vinyl chloride, other modifying resins, and plasticizers.
- Vinyl resins are tough, chemically inert, thermoplastic, and resistant to many solvents.
- Vinyl composition tiles are formed into solid sheets of varying thicknesses (1/8-inch (0.32-cm) is most common) by applying heat and pressure to colored vinyl chips, and are typically cut into squares (e.g., 12-inch (30-cm) squares).
- VC tile may be supplied with a surface finish layer, but is otherwise generally substantially uniform in appearance throughout its thickness.
- Maintenance of installed VC tile flooring typically involves coating with several coats of a clear polymeric floor finish to achieve satisfactory gloss, followed by frequent (e.g., daily) dusting and burnishing, less frequent scrubbing, and occasional stripping and recoating with floor finish to maintain its appearance.
- VC tile flooring e.g., VC tile having one or more layers of floor finish thereon
- stains due to spills e.g., of iodine antiseptic
- replacement of the floor tile is the typical remedy; however, this process is time consuming and expensive.
- methods according to the present disclosure can postpone the need for replacement of VC tile (e.g., for years), thereby saving time, cost, and reducing environmental waste.
- methods according to the present disclosure can be used instead of strip and recoat operations, whereby they can significantly reduce the mess and time required to refurbish the floor appearance.
- the present disclosure provides a method of refurbishing vinyl composition tile flooring, the method comprising sequential steps:
- first structured abrasive members affixed to a first machine driver pad
- first structured abrasive members comprising first shaped abrasive composites affixed to a first compliant backing
- first shaped abrasive composites comprise first abrasive particles dispersed in a first polymeric binder, wherein the first abrasive particles have a first average particle size
- average surface roughness R a of said at least a portion of the exposed surface of the floor decreases during each of steps a) and b).
- the method further comprises, after step b):
- the method further comprises, subsequent to step b) or step c) (if included), applying a clear polymeric finish to said at least a portion of the exposed surface of the floor.
- the present disclosure provides a method of refurbishing vinyl flooring, the method comprising sequential steps:
- first structured abrasive members affixed to a first machine driver pad
- the first structured abrasive members comprising first shaped abrasive composites affixed to a first compliant backing, wherein the first shaped abrasive composites comprise second abrasive particles dispersed in a second polymeric binder, wherein the second abrasive particles have a second average particle size that is smaller than the first average particle size
- the method further comprises, after step c):
- the method further comprises, subsequent to step c) or step d) (if included), applying a clear polymeric finish to the abraded exposed surface of the floor.
- the term "compliant" means yielding and/or conforming in response to applied pressure;
- the term “(meth)acryl” refers to acryl and/or methacryl;
- polymer and “polymeric” refer to an organic polymer
- subsequent means at a later time, which may be immediate or at a later time (e.g., after one or more intervening abrading steps or other processes or events);
- wet abrading refers to abrading in the presence of water, the water optionally containing one or more additional components such as, for example, organic solvents, pH modifiers, colorants, dyes, fragrances, disinfectants, and surfactants.
- surface roughness R a and R z are as defined in the Examples section hereinbelow.
- FIG. 1A is a schematic side view of an exemplary structured abrasive member 100 useful in practice of the present disclosure.
- FIG. IB is an enlarged view of region IB in FIG. 1A.
- FIG. 1 C is a schematic side view of an exemplary structured abrasive member 105 useful in practice of the present disclosure.
- FIG. 2 is a schematic perspective bottom view of an exemplary arrangement of structured abrasive members affixed to a compressible resilient machine driver pad useful in practice of methods according to the present disclosure.
- Methods according to the present disclosure are suitable for refurbishing vinyl composition tile flooring.
- the flooring to be refurbished should be inspected and cracked, raised and/or blistered, or broken tiles replaced.
- preexisting floor finish may be removed using conventional wet stripping techniques.
- preexisting floor finish is removed using an aggressive nonwoven abrasive member; for example, a floor finish stripping pad used in conventional wet stripping processes.
- the area of the floor involved is cordoned off from public access during the refurbishing process.
- a method of refurbishing vinyl flooring comprises wet abrading an exposed surface of a floor comprising vinyl composition tiles with first structured abrasive members affixed to a first compressible resilient machine driver pad, and then wet abrading the exposed surface of the floor with second structured abrasive members affixed to a second compressible resilient machine driver pad. In some embodiments, the method then further comprises wet abrading the exposed surface of the floor with third structured abrasive members affixed to a third compressible resilient machine driver pad.
- the abraded portion of a typical VC tile floor is smoother (has less roughness) than before the abrading step.
- the degree of roughness will depend on the initial roughness before abrading, the duration and applied force while abrading, the nature of the abrasive member, and the abrasive particle size.
- the average surface roughness R a may be less than or equal to 120 microinches (3.05 microns) (e.g., after wet abrading with a
- 300- ⁇ diamond structured abrasive disc 95 microinches (2.41 microns) (e.g., after wet abrading with a 45- ⁇ diamond structured abrasive disc), 80 microinches (2.03 microns) (e.g., after wet abrading with a 10- ⁇ diamond structured abrasive disc) down to 70 microinches (1.78 microns), 60 microinches (1.52 microns), 50 microinches (1.27 microns), 40 microinches (1.02 microns), 30 microinches (0.76 microns) (e.g., after wet abrading with a 6- ⁇ diamond structured abrasive disc), or 20 microinches (0.51 microns), or even less than 10 microinches (0.25 microns) (e.g., after wet abrading with a 3- ⁇ diamond structured abrasive disc).
- the surface roughness R z of the abraded portion of the VC tile floor, after wet abrading with structured abrasive members e.g., steps a), b), and c); or steps b), c), and d;
- microinches (17.8 microns) (e.g., after wet abrading with a 300- ⁇ diamond structured abrasive disc), 600 microinches (15.2 microns) (e.g., after wet abrading with a 45- ⁇ diamond structured abrasive disc), 525 microinches (13.3 microns) (e.g., after wet abrading with a 10- ⁇ diamond structured abrasive disc) down to 500 microinches (12.7 microns), 430 microinches (10.9 microns), 360 microinches (9.14 microns), 280 microinches (7.1 1 microns), 180 microinches (4.57 microns) (e.g., after wet abrading with a 6- ⁇ diamond structured abrasive disc), or 150 microinches (3.81 microns), or even less than 100 microinches (2.54 microns) (e.g., after wet abrading with a 3- ⁇ diamond structured a
- exemplary structured abrasive member 100 comprises structured abrasive layer 110 disposed on first surface 122 of compliant backing 120.
- Optional attachment interface system 130 is secured to second surface 124 of compliant backing 120 by adhesive layer 135.
- Optional attachment interface system 130 further includes looped portion 160 of a hook and loop fastener, and hooked interface pad 150 having hooked portions of a hook and loop fastening system on opposing sides thereof.
- Structured abrasive layer 1 10 comprises a plurality of shaped abrasive composites 140, which are composites of abrasive particles 145 distributed in a binder 148 (e.g., see FIG. IB).
- the shaped abrasive composites are rigid.
- Shaped abrasive composites 140 are separated by a boundary or boundaries associated with the shape of the shaped abrasive composite, resulting in one shaped abrasive composite being separated to some degree from adjacent abrasive composites.
- One of the earliest references to abrasive articles with shaped abrasive composites is U.S. Patent No.
- abrasive composite refers to abrasive composites having a shape that has been formed by curing a curable flowable mixture of abrasive particles and curable binder precursor while the mixture is both being borne on a backing and filling a cavity on the surface of a production tool.
- Such a precisely-shaped abrasive composites have precisely the same shape as that of the cavity.
- a plurality of such composites provide three-dimensional shapes that project outward from the surface of the backing in a non- random pattern, namely the inverse of the pattern of the production tool.
- Useful compliant backings 120 may include those known useful in abrasive articles such as, for example, metal, thick polymeric sheets and/or films (e.g., polycarbonate), saturant-treated cloths (e.g., glass and/or polyester cloth) and nonwoven fabrics, treated or primed versions thereof, and combinations thereof. Examples include polyester sheets, polyolefin sheets (e.g., polyethylene and propylene sheet), polyamide sheets, polyimide sheets, and polycarbonate sheets.
- Abrasive particles 145 may comprise, for example, fused aluminum oxide (including white fused alumina, heat-treated aluminum oxide, and brown aluminum oxide), ceramic aluminum oxide (including shaped ceramic alumina particles), heated treated aluminum oxide, silicon carbide, diamond (natural and synthetic), cubic boron nitride, boron carbide, titanium carbide, cubic boron nitride, garnet, fused alumina-zirconia, diamond, zirconia, and combinations thereof. Of these, diamonds are preferred. Useful diamonds may be either natural diamonds or man-made diamonds. The diamonds may include a surface coating (e.g., nickel or other metal) to improve the retention of the diamonds in the resin matrix.
- fused aluminum oxide including white fused alumina, heat-treated aluminum oxide, and brown aluminum oxide
- ceramic aluminum oxide including shaped ceramic alumina particles
- heated treated aluminum oxide silicon carbide
- diamond naturally and synthetic
- cubic boron nitride boron carbide
- titanium carbide titanium carbide
- Abrasive particles 145 may also be present in abrasive aggregates. Such aggregates comprise a plurality of the abrasive particles, a matrix material, and optional additives.
- the matrix material may be organic and/or inorganic.
- the matrix material can be, for example, polymer resin, glass (e.g., vitreous-bond diamond aggregates), metal, glass-ceramic, ceramic (e.g., ceramic-bond agglomerates as described in U.S. Patent No. 6,790,126 (Wood et al.)), or a combination thereof.
- glass such as silica glass, glass-ceramics, borosilicate glass, phenolic, epoxy, acrylic, and the other resins described in the context of the composite binder can be used as the matrix material.
- Abrasive aggregates may be randomly shaped or have a predetermined shape associated with them. Additional details regarding various abrasive aggregates and methods of making them may be found, for example, in U.S. Patent Nos.
- Vitreous-bond abrasive aggregates can be made, for example, by providing a plurality of glass bodies made from the glass binder, each glass body having a defined shape, and glass bodies having a softening temperature, providing a plurality of abrasive particles, mixing the plurality of glass bodies and the plurality of abrasive particles together to form a mixture, heating the mixture to the softening temperature of glass bodies so that glass bodies soften while substantially retaining the defined shape, adhering abrasive particles to the softened glass bodies to form a plurality of abrasive aggregates, and cooling abrasive aggregates so that the glass binder of glass bodies hardens. Further details are described in U.S. Patent No.
- the abrasive particles may further comprise a surface treatment or coating such as, for example, a coupling agent or metal or ceramic coating.
- a surface treatment or coating such as, for example, a coupling agent or metal or ceramic coating.
- the abrasive particles have a Mohs hardness of at least 7, preferably at least 8, and more preferably at least 9.
- the abrasive particles preferably have an average particle size in a range of from about 0.01 micrometer (small particles) to 500 micrometers (large particles), more preferably about 0.25 micrometers to about 500 micrometers, even more preferably about 3 micrometers to about 400 micrometers, and most preferably about 5 micrometers to about 50 micrometers.
- abrasive particle sizes are reported as "mesh” or "grade", both of which are commonly known abrasive particle sizing methods.
- abrasive particle size will typically depend on the point in the refurbishing process of the present disclosure at which it is to be used, with the average size of the abrasive particles decreasing with each successive structured abrasive member (e.g., first, then second, and optionally then third).
- Shaped abrasive composites 140 may optionally include diluent particles, which are not sufficiently hard to serve effectively as abrasive particles.
- the particle size of these diluent particles may be on the same order of magnitude as the abrasive particles. Examples of such diluent particles include gypsum, marble, limestone, flint, silica, glass bubbles, glass beads, and aluminum silicate.
- Abrasive particles 145 are adhered one to another with binder 148 to form shaped abrasive composites 140 (e.g., see FIG. IB).
- Binder 148 is an organic and/or polymeric binder, and is derived from a binder precursor.
- abrasive particles 145 are present in vitreous-bond abrasive aggregates (not shown).
- the binder precursor is exposed to an energy source which aids in the initiation of polymerization or curing of the binder precursor.
- energy sources include thermal energy and radiation energy, the latter including electron beam, ultraviolet light, and visible light.
- the binder precursor is polymerized or cured and is converted into a solidified binder.
- the adhesive matrix is formed.
- Binder 148 can be formed, for example, of a curable (via energy such as UV light or heat) organic binder precursor material.
- a curable (via energy such as UV light or heat) organic binder precursor material examples include alkylated urea-formaldehyde resins, melamine-formaldehyde resins, and alkylated benzoguanamine-formaldehyde resin, acrylate resins (including acrylates and methacrylates) such as vinyl acrylates, acrylated epoxies, acrylated urethanes, acrylated polyesters, acrylated acrylics, acrylated polyethers, vinyl ethers, acrylated oils, and acrylated silicones, alkyd resins such as urethane alkyd resins, polyester resins, reactive urethane resins, phenolic resins such as resole and novolac resins, phenolic/latex resins, epoxy resins such as bisphenol epoxy resins, isocyanates, is
- the resins may be provided as monomers, oligomers, polymers, or combinations thereof.
- the binder precursor may include one or more of photoinitiators, crosslinkers, thermal initiators, catalysts, and combinations thereof. Such materials are well known in the art.
- Embossing and/or screen printing may also be used to form shaped abrasive composites as described in, for example, U.S. Patent No. 5,014,468 (Ravipati et al.).
- the structured abrasive members may have any shape such as, for example, discs, squares, daisies, rectangular strips, rings, crescents, spirals, wavy lines, or any 2-dimensional geometric shape.
- Examples of commercially available structured abrasive members suitable for use in the present disclosure include, for example, those available as 3M TRIZACT DIAMOND HX Gold, Red, and Blue discs from 3M Company, St. Paul, Minnesota.
- Optional attachment interface system 130 may comprise, for example, the hooked portion of a hook and loop fastening system, or capped stems of a self-mating mechanical fastener (e.g., as described in U.S. Patent Nos. 5672186 (Chesley et al.) or 5,201,101 (Rouser et al.)).
- Optional attachment interface system may comprise multiple elements such as, for example, a looped portion of a hook and loop fastener in combination with an interface pad having hooked portions of a hook and loop fastener on opposite sides thereof, thereby providing a hooked outer surface for mounting to the machine driver pad.
- exemplary structured abrasive member 105 comprises structured abrasive layer 1 10 disposed on first surface 122 of compliant backing 120.
- Attachment interface system 137 is secured to second surface 124 of compliant backing 120 by adhesive layer 135.
- attachment interface system 137 comprises one half of a capped- stem self-mating fastener comprising foam layer 170, auxiliary adhesive layer 175, and capped stem backing 180.
- other attachment interface systems having hook-type projections may also be used (e.g., J-hook fasteners and T-hook fasteners).
- Suitable optional interface layers are typically compressible and conformable.
- the optional attachment layer has sufficient overall thickness that it raises the structured abrasive members beyond the surface of machine driver pad to which it is attached, so that the machine driver pad does not substantially reduce the contact pressure between the structured abrasive members and the floor surface.
- the optional interface layer may have a thickness in a range of from 2 millimeters to 13 millimeters, preferably from 2 millimeters to 5 millimeters.
- the optional attachment interface system is not present, then some other method for mounting the pads (e.g., such as adhesive) may be used. In such cases, and indeed in most instances, it may be desirable multiple to securely mount structured abrasive members to the compressible resilient nonwoven machine driver pad to form an assembly for each type of structured abrasive member used. Accordingly, to change from one structured abrasive member type to another it is only necessary to change structured abrasive member/compressible resilient machine driver pad assemblies, instead of remounting individual structured abrasive members.
- some other method for mounting the pads e.g., such as adhesive
- the first, second, and optional third structured abrasive members independently comprise shaped abrasive composites affixed to a compliant backing (i.e., the backing is prone to irreversible mechanical damage if subjected to more than incidental flexing).
- Each of the shaped abrasive composites comprises abrasive particles dispersed in a first polymeric binder.
- the average particle size of abrasive particles in each successive structured abrasive member is smaller than the previous one, thereby resulting in ever increasing levels of smoothness, while achieving reasonable overall abrading rates.
- the shaped abrasive composites of the structured abrasive members contained ever decreasing particle sizes, the other components such as for example, binder abrasive particle composition, compliant backing, and size, shape, and/or arrangement of the abrasive composites may change. In some circumstances, this may lead to increase in surface roughness of the VC tile floor, and such combination of structured abrasive members should generally be avoided, or followed by additional abrading steps to smooth the floor surface.
- the structured abrasive members be substantially the same (e.g., in terms of the shape, size, composition, and arrangement of the shaped abrasive composites, composition of abrasive particles, and /or the compliant backing), except for the average size of the abrasive particles.
- the machine driver pads may be made of any material capable of supporting the structured abrasive members (e.g., metal plates, nonwoven pads, foams, rubber discs).
- machine driver pads are capable of compressing and recovering without substantial permanent deformation (i.e., they are compressible and resilient). Compressibility and resiliency allow the machine driver pad to float over gradual irregularities in height of the floor (which may be cause, for example, by an underlying concrete surface), whereas a rigid machine driver pad may be prone to gouging the floor in such circumstances (e.g., depending on the floor maintenance machine design).
- the machine driver pads comprise nonwoven material having a disc-shape (although other shapes may also be used) and having a thickness and compressibility typically of a conventional buffing pad for a swing arm buffing machine.
- the machine driver pads may comprise a nonwoven fiber disc having a thickness in a range of from 1 to 5 centimeters (cm) and a diameter in a range of from 0.3 to 1 meter.
- Useful nonwoven materials may comprise, for example, synthetic fibers (e.g., polyester, polyamide, polyolefin, and bicomponent core-shell synthetic fibers), natural fibers (e.g., banana, flax, cotton, jute, agave, sisal, coconut, soybean, and hemp), and combinations of the foregoing.
- the machine driver pad may have abrasive particles bonded to nonwoven fibers.
- Lofty nonwoven machine driver pads may be prepared according to conventional methods such as, for example, by forming a low density air-laid fiber web using a Rando Webber web- forming machine commercially available from Rando Machine Corporation, Ard, New York.
- a blend of fibers may be used.
- One exemplary such blend includes polyester (polyethylene terephthalate) staple fibers and crimped sheath-core melt-bondable polyester staple fibers.
- the fiber web is then optionally heated in a hot convection oven to activate any melt- bondable fibers in the fiber web and pre-bond the web. Examples of suitable melt-bondable fibers are described in U.S. Patent No. 5,082,720 (Hayes).
- the fibers are preferably tensilized and crimped, but may also be continuous filaments such as those formed by an extrusion process, e.g., as described in U.S. Patent No. 4,227,350 (Fitzer).
- the optionally pre-bonded fiber web is then coated with a liquid binder precursor composition by passing it between the coating rolls of a two roll coater, wherein the bottom coating roll is partially immersed in the liquid binder resin composition.
- exemplary liquid binder precursor compositions include aminoplasts, urea-formaldehyde resins, phenolics, epoxies, and urethanes, although other binder precursors may also be used.
- the coated nonwoven web is then placed in an oven heated to cure the liquid binder precursor resin, and produce a bonded nonwoven web.
- the machine driver pad comprises an open nonwoven fiber substrate (e.g., a nonwoven fiber disc) that has no external backing layer.
- Suitable nonwoven compressible resilient backings are also available from commercial sources such as, for example, 3M WHITE SUPER POLISH PAD 4100 , 3M RED BUFFER PAD 5100, and 3M NATURAL BLEND WHITE PAD 3300 floor pads all from 3M Company, St. Paul., MN.
- the compressible resilient backing may comprise a foam (e.g., a foam disc).
- Laminate constructions such as, for example, foam and nonwoven fiber web laminate may also be used.
- VC tile is generally substantially uniform in appearance throughout its thickness.
- VC tile is widely available from commercial suppliers such as, for example, Armstrong World Industries, Inc., Lancaster, Pennsylvania; Mannington Mills, Salem, New Jersey; and Congoleum Corp., Mercerville, New Jersey.
- the structured abrasive members are secured to the compressible resilient backing (e.g., the first structured abrasive members, the second structured abrasive members, or optionally the third structured abrasive members), which in turn is typically mounted to a low speed (i.e., from about 175 to about 350 revolutions per minute) mechanical device of the type used to maintain VC tile flooring. Examples include manually operated rotary floor machines and walk-behind or riding autoscrubbers.
- FIG. 2 shows an exemplary assembly 200 of structured abrasive members 100 affixed to a machine driver pad 210 that is useful in practice of the present disclosure.
- any appropriate number of structured abrasive members may be used (e.g., the number of structured abrasive members may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more), in any arrangement.
- the structured abrasive members are symmetrically arranged on the surface of the compressible resilient machine driver pad, although other arrangements may also be used.
- the structured abrasive members are typically positioned so that they are adjacent the peripheral edge of the compressible resilient machine driver pad, although other arrangements may also be used.
- a non- woven pad having diamonds bonded thereto may be useful for final burnishing of the VC tile flooring after the wet abrading steps (e.g., a), b), and optionally c)) with structured abrasive members.
- wet abrading steps e.g., a), b), and optionally c)
- structured abrasive members examples include those available as 3M SCOTCH-BRITE PURPLE DIAMOND FLOOR PAD PLUS and 3M SCOTCH-BRITE SIENNA DIAMOND FLOOR PAD PLUS from 3M Company.
- Such pads may also be used in one or more additional slow speed wet abrading steps that can optionally be used to augment processes according to the present disclosure.
- High-speed burnishing e.g., at speeds in excess of 1000 revolutions per minute
- High speed burnishing can be carried out using methods well known in the art, for example, using a electric, battery, or propane burnishing machine.
- VC tile flooring may be pre-conditioned so that it is more suited to abrading according to the present disclosure.
- existing floor finish may be removed using a chemical stripper and a nonwoven stripping pad.
- chemical stripping is omitted as it is messy, time consuming, and aesthetically unpleasant. Accordingly, in some embodiments, no pre-conditioning step is used, while in others, an aggressive abrasive floor pad is used to remove the finish without aid of stripper (although water may be useful for dust control).
- Examples of such aggressive abrasive floor pads are available as 3M BLACK STRIPPER PAD 7200, 3M BROWN STRIPPER PAD 7100, 3M HIGH PRODUCTIVITY PAD 7300, and 3M CLEAN AND STRIP XT floor pads, all from 3M Company.
- first structured abrasive members affixed to the first compressible resilient machine driver pad
- the first structured abrasive members comprising first shaped abrasive composites affixed to a first compliant backing
- the first shaped abrasive composites comprise first abrasive particles dispersed in a first polymeric binder, wherein the first abrasive particles have a first average particle size.
- the first average particle size is in a range of from 200 to 400 microns, preferably from 250 to 350 microns.
- the process is repeated again using the second structured abrasive members with second abrasive particles having a second average particle size that is smaller than the first average particle size.
- the second average particle size is in a range of from 25 to 75 microns, preferably from 35 to 65 microns.
- the floor may be sufficiently restored for use.
- additional wet abrading processes as above, but using successively smaller average abrasive particle sizes.
- a clear polymeric finish may be applied to enhance appearance and protect the floor from wear.
- the clear polymeric finish may include water-soluble or water-dispersible film formers such as metal-free acrylic finishes, acid-containing polymers crosslinked using transition metals, and water-soluble or water-dispersible multicomponent (e.g., two-component) polyurethanes.
- the clear polymeric finish may contain mixtures of film formers.
- suitable commercially available clear polymeric finishes include acrylic floor finishes 3M SCOTCHGARD VINYL FLOOR PROTECTOR, 3M CORNERSTONE, 3M
- the present disclosure provides a method of refurbishing vinyl composition tile flooring, the method comprising sequential steps: a) wet abrading at least a portion of an exposed surface of a floor comprising vinyl composition tiles with first structured abrasive members affixed to a first machine driver pad, the first structured abrasive members comprising first shaped abrasive composites affixed to a first compliant backing, wherein the first shaped abrasive composites comprise first abrasive particles dispersed in a first polymeric binder, wherein the first abrasive particles have a first average particle size; and
- average surface roughness R a of said at least a portion of the exposed surface of the floor decreases during each of steps a) and b).
- the present disclosure provides a method according to the first embodiment, wherein average surface roughness R z of said at least a portion of the exposed surface of the floor decreases during each of steps a) and b).
- each of the first structured abrasive members further comprise a first attachment interface system secured to the first compliant backing, the first attachment interface system having a plurality of loops opposite the first compliant backing, wherein the first structured abrasive members are affixed to the first machine driver pad by a first attachment interface member having two opposed major faces having hooks extending therefrom.
- each of the first structured abrasive members further comprise a first compliant foam layer secured to the first compliant backing, and an attachment interface system having a plurality of hooks opposite the first compliant foam layer.
- each of the second structured abrasive members further comprise a second compliant foam layer secured to the second compliant backing, and an attachment interface system having a plurality of hooks opposite the second compliant foam layer.
- each of the second structured abrasive members further comprises a second attachment interface system secured to the second compliant backing, the second attachment interface system having a plurality of loops opposite the second compliant backing, wherein the second structured abrasive members are affixed to the second machine driver pad by an attachment interface member having two opposed major faces having hooks extending therefrom.
- the present disclosure provides a method according to any of the first to sixth embodiments, wherein the first and second machine driver pads are compressible and resilient.
- the present disclosure provides a method according to any of the first to seventh embodiments, wherein the first shaped abrasive composites, the second shaped abrasive composites, or both, are precisely-shaped.
- the present disclosure provides a method according to any of the first to eighth embodiments, wherein the first average particle size is in a range of from 400 microns to 600 microns.
- the present disclosure provides a method according to any of the first to ninth embodiments, wherein the second average particle size is in a range of from 25 microns to 75 microns.
- the present disclosure provides a method according to any of the first to tenth embodiments, wherein at least one of the first or second shaped abrasive composites comprises superabrasive particles retained in a vitreous binder.
- the present disclosure provides a method according to any of the first to eleventh embodiments, wherein after step b) the average surface roughness R a of said at least a portion of the exposed surface of the floor is less than or equal to 95 microinches.
- the present disclosure provides a method according to any of the first to twelfth embodiments, further comprising, after step b):
- the present disclosure provides a method according to any of the first to thirteenth embodiments, wherein after step c), the abraded exposed surface of the floor has an average surface roughness of less than 80 microinches.
- the present disclosure provides a method according to any of the first to fourteenth embodiments, further comprising, subsequent to step b), applying a clear polymeric finish to said at least a portion of the exposed surface of the floor.
- the present disclosure provides a method of refurbishing vinyl flooring, the method comprising sequential steps:
- first structured abrasive members affixed to a first machine driver pad
- the first structured abrasive members comprising first shaped abrasive composites affixed to a first compliant backing, wherein the first shaped abrasive composites comprise second abrasive particles dispersed in a second polymeric binder, wherein the second abrasive particles have a second average particle size that is smaller than the first average particle size
- the present disclosure provides a method according to the sixteenth embodiment, wherein the nonwoven abrasive member comprises a floor finish stripping pad.
- the present disclosure provides a method according to the sixteenth or seventeenth embodiment, wherein average surface roughness R z of said at least a portion of the exposed surface of the floor decreases during each of steps a) and b).
- each of the first structured abrasive members further comprise a first compliant foam layer secured to the first compliant backing, and an attachment interface system having a plurality of hooks opposite the first compliant foam layer.
- each of the second structured abrasive members further comprise a second compliant foam layer secured to the second compliant backing, and an attachment interface system having a plurality of hooks opposite the second compliant foam layer.
- each of the first structured abrasive members further comprise a first attachment interface system secured to the first compliant backing, the first attachment interface system having a plurality of loops opposite the first compliant backing, wherein the first structured abrasive members are affixed to the first machine driver pad by a first attachment interface member having two opposed major faces having hooks extending therefrom.
- each of the second structured abrasive members further comprises a second attachment interface system secured to the second compliant backing, the second attachment interface system having a plurality of loops opposite the second compliant backing, wherein the second structured abrasive members are affixed to the second machine driver pad by an attachment interface member having two opposed major faces having hooks extending therefrom.
- the present disclosure provides a method according to any of the sixteenth to twenty-second embodiments, wherein the first and second machine driver pads are compressible and resilient.
- the present disclosure provides a method according to any of the sixteenth to twenty-third embodiments, wherein the first shaped abrasive composites, the second shaped abrasive composites, or both, are precisely-shaped.
- the present disclosure provides a method according to any of the sixteenth to twenty-fourth embodiments, wherein the second average particle size is in a range of from 400 microns to 600 microns.
- the present disclosure provides a method according to any of the sixteenth to twenty-fifth embodiments, wherein the third average particle size is in a range of from 25 microns to 75 microns.
- the present disclosure provides a method according to any of the sixteenth to twenty-sixth embodiments, wherein at least one of the first or second shaped abrasive composites comprises superabrasive particles retained in a vitreous binder.
- the present disclosure provides a method according to any of the sixteenth to twenty-seventh embodiments, wherein after step c) the average surface roughness R a of the abraded exposed surface of the floor is less than or equal to 2.4 microns.
- the present disclosure provides a method according to any of the sixteenth to twenty-eighth embodiments, further comprising, after step c):
- the present disclosure provides a method according to any of the sixteenth to twenty-ninth embodiments, wherein after step d), the average surface roughness R a of said at least a portion of the exposed surface of the floor is less than or equal to 80 microinches.
- the present disclosure provides a method according to any of the sixteenth to thirtieth embodiments, further comprising, subsequent to step c), applying a clear polymeric finish to said at least a portion of the exposed surface of the floor.
- 3M SCOTCHGARD VINYL FLOOR PROTECTOR is an aqueous mixture of a polymer and nano-sized, inorganic particles, designed for use as a floor protector from 3M Company.
- T300 refers to a 5-inch (13-centimeter) diameter 300- ⁇ diamond structured abrasive disc, having microreplicated composite diamond abrasive structures on a flexible cloth backing, supplied with a 3M hook mounting disc, and obtained under the trade designation "3M TRIZACT DIAMOND HX GOLD" from 3M Company.
- T45 refers to a 5-inch (13-centimeter) diameter 45- ⁇ diamond structured abrasive disc, having microreplicated composite diamond abrasive structures on a flexible cloth backing, supplied with a 3M hook mounting disc, and obtained under the trade designation "3M TRIZACT DIAMOND HX RED” from 3M Company.
- T10 refers to a 5-inch (13-centimeter) diameter 10- ⁇ diamond structured abrasive disc, having microreplicated composite diamond abrasive structures on a flexible cloth backing, supplied with a 3M hook mounting disc, and obtained under the trade designation "3M TRIZACT DIAMOND HX BLUE” from 3M Company.
- T6 refers to a 5-inch (13-centimeter) diameter 6- ⁇ diamond structured abrasive disc, having microreplicated composite diamond abrasive structures on a 5-mil (130-micron) film laminated to a polycarbonate backing, obtained under the trade designation "3M TRIZACT 673LA grade A6" from 3M Company.
- T3 refers to a 5-inch (13-centimeter) diameter 3- ⁇ diamond structured abrasive disc, having microreplicated composite diamond abrasive structures on a 5-mil (130-micron) film laminated to a polycarbonate backing, "3M TRIZACT 673LA grade A3" from 3M Company.
- PDP refers to a 20-inch (43 -centimeter) diameter diamond abrasive nonwoven floor polishing pad, obtained under the trade designation "3M SCOTH-BRITE PURPLE DIAMOND FLOOR PAD PLUS" from 3M Company.
- WSP1 refers to a 17-inch (43 -centimeter) diameter nonwoven floor polishing pad, obtained under the trade designation "3M WHITE SUPERPOLISH PAD 4100" from 3M
- WSP2 refers to a 20-inch (43 -centimeter) diameter nonwoven floor polishing pad, obtained under the trade designation "3M WHITE SUPERPOLISH PAD 4100" from 3M
- the surface roughness of the vinyl composite (VC) tile is defined by R z and R a .
- the R a of a surface is the measurement of the arithmetic average of the scratch depth. It is the average of 5 individual roughness depths of five successive measuring lengths, where an individual roughness depth is the vertical distance between the highest point and a center line.
- R z is the average of 5 individual roughness depths of a measuring length, where an individual roughness depth is the vertical distance between the highest point and the lowest point.
- Surface roughness data reported in Table 1 are the average of six measurements taken on six VC tile specimens, using a profilometer, available under the trade designation "SURTRONIC 25 PROFILOMETER” from Taylor Hobson, Inc., Sheffield, England.
- the gloss of the VC tile samples was measured at angles of 20, 60 and 85 degrees using a gloss meter, model "4430", obtained from BYK-Gardner, Columbia, Maryland. Gloss data reported in Tables 1 and 2 are the average of six measurements taken on six VC tile specimens.
- DSCF Dry Static Coefficient of Friction
- An interface pad having hooks on both surfaces, supplied with the diamond structured abrasive discs (above) was attached to a swing-type floor machine equipped with a WSPl machine driver pad which operates at 175 revolutions per minute.
- Four T300 discs were then attached to the interface pad and the test area honed four times with the floor machine at 88 ft/min (26.82 meters/min).
- Surface finish, gloss and dry static coefficient of friction values were then measured.
- the T300 discs were replaced with T45 discs and the process repeated, after which the surface finish, gloss and dry static coefficient of friction values were again measured.
- the abrading process continued using successively finer T10 abrading discs. Surface finish, gloss and dry static coefficient of friction values were measured after each abrading step.
- E- 1 Half of the test area was marked off and designated "E- 1 " for Example 1 , and the other half designated "E-2" for Example 2.
- the T10 abrading discs were replaced with T6 discs and the Area E-2 abraded four times with the floor machine at 88 ft/min (26.82 meters/min).
- the T6 discs were then replaced with T3 discs and area E-2 was again abraded in the same manner.
- the entire test areas of E- 1 and E-2 were then burnished by six passes using a high speed burnisher, model "SPEEDSHINE 2000", obtained Tennant Trend, Inc., Holland, Michigan, with a PDP floor abrading pad, at 88 ft/min (26.82 meters/min) (1 st PDP step).
- a vinyl composition tile protector trade designation "3M SCOTCHGARD VINYL FLOOR PROTECTOR” from 3M Company, was applied to the burnished area using a "3M EASY SHINE APPLICATOR SYSTEM” and the burnishing step repeated (2 nd PDP step), followed by six passes with a WSP2 floor pad (1 st WSP step). The entire test area was again coated with the vinyl floor protector, then burnished again with the PDP and the WSP floor pads as described above (3 rd PDP and 2 nd WSP steps, respectively). Surface finish, gloss and dry static coefficient of friction values were then measured for both areas E-l and E-2. Results are reported in Table 1 (below).
- Example 3 used structured abrasive discs to prepare the floor for coating with 3M SCOTCHGARD VINYL FLOOR PROTECTOR as described below.
- Comparative Example A used the floor preparation procedure outlined in the 3M SCOTCHGARD VINYL FLOOR PROTECTOR Technical Data sheet (dated February 2011) to prepare the floor. After floor preparation, both examples followed the 3M SCOTCHGARD VINYL FLOOR PROTECTOR Technical Data sheet (dated February 2011) application procedure.
- Example 3 the floor was treated as follows:
- Examples 4 - 10 and Comparative Examples B-C used structured abrasive discs in different combinations to prepare the floor for coating with 3M SCOTCHGARD VINYL FLOOR
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BR112014005560A BR112014005560A2 (pt) | 2011-09-12 | 2012-08-28 | método de renovação de ladrilho composto de vinila e método de renovação de pisos vinílicos |
CN201280043598.1A CN103781593B (zh) | 2011-09-12 | 2012-08-28 | 再磨光乙烯基组合物瓷砖的方法 |
MX2014002837A MX2014002837A (es) | 2011-09-12 | 2012-08-28 | Metodo de renovacion de loseta de composicion vinilica. |
CA2848294A CA2848294A1 (en) | 2011-09-12 | 2012-08-28 | Method of refurbishing vinyl composition tile |
KR1020147009480A KR20140075712A (ko) | 2011-09-12 | 2012-08-28 | 비닐 조성물 타일의 재생 방법 |
JP2014529762A JP2014528845A (ja) | 2011-09-12 | 2012-08-28 | ビニル組成物タイルを改修する方法 |
EP12766744.2A EP2755799A1 (en) | 2011-09-12 | 2012-08-28 | Method of refurbishing vinyl composition tile |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/230,287 US20130065490A1 (en) | 2011-09-12 | 2011-09-12 | Method of refurbishing vinyl composition tile |
US13/230,287 | 2011-09-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013039688A1 true WO2013039688A1 (en) | 2013-03-21 |
Family
ID=46964014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2012/052660 WO2013039688A1 (en) | 2011-09-12 | 2012-08-28 | Method of refurbishing vinyl composition tile |
Country Status (9)
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SG11201500802TA (en) * | 2012-08-02 | 2015-04-29 | 3M Innovative Properties Co | Abrasive articles with precisely shaped features and method of making thereof |
CN115625629A (zh) * | 2012-08-02 | 2023-01-20 | 3M创新有限公司 | 具有精确成形特征部的研磨元件、用其制成的研磨制品及其制造方法 |
US20150065012A1 (en) * | 2013-08-27 | 2015-03-05 | 3M Innovative Properties Company | Method of finishing a stone surface and abrasive article |
JP6623153B2 (ja) | 2013-11-12 | 2019-12-18 | スリーエム イノベイティブ プロパティズ カンパニー | 構造化研磨物品並びにその使用方法 |
JP6728568B2 (ja) * | 2014-03-27 | 2020-07-22 | 大日本印刷株式会社 | シート |
JP6838811B2 (ja) * | 2014-05-02 | 2021-03-03 | スリーエム イノベイティブ プロパティズ カンパニー | 断続的構造化研磨物品並びに被加工物の研磨方法 |
US9926477B2 (en) | 2014-12-31 | 2018-03-27 | Saint-Gobain Abrasives, Inc. | Aggregates of diamond with vitrified bond |
CN106064340B (zh) * | 2015-04-23 | 2020-09-29 | 内陆钻石制品公司 | 地板抛光垫 |
WO2018119275A1 (en) | 2016-12-23 | 2018-06-28 | Saint-Gobain Abrasives, Inc. | Coated abrasives having a performance enhancing composition |
EP3764865B1 (en) * | 2018-03-13 | 2024-08-07 | 3M Innovative Properties Company | Floor bristle brush assembly |
CN109015435B (zh) * | 2018-09-10 | 2025-01-03 | 台山市远鹏研磨科技有限公司 | 一种金刚石塔型砂纸 |
KR20220033497A (ko) * | 2019-07-08 | 2022-03-16 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 세정 및 폴리싱 유체 및 사용 방법 |
CN112792620A (zh) * | 2020-12-31 | 2021-05-14 | 成都中车四方轨道车辆有限公司 | 一种轨道列车车厢橡胶布修旧如新的工艺 |
CN113199365A (zh) * | 2021-05-08 | 2021-08-03 | 乔冠应用材料(淮安)有限公司 | 一种铜材料全自动研磨机及研磨方法 |
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- 2012-08-28 JP JP2014529762A patent/JP2014528845A/ja active Pending
- 2012-08-28 KR KR1020147009480A patent/KR20140075712A/ko not_active Withdrawn
- 2012-08-28 CA CA2848294A patent/CA2848294A1/en not_active Abandoned
- 2012-08-28 MX MX2014002837A patent/MX2014002837A/es unknown
- 2012-08-28 CN CN201280043598.1A patent/CN103781593B/zh not_active Expired - Fee Related
- 2012-08-28 EP EP12766744.2A patent/EP2755799A1/en not_active Withdrawn
- 2012-08-28 WO PCT/US2012/052660 patent/WO2013039688A1/en active Application Filing
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Also Published As
Publication number | Publication date |
---|---|
JP2014528845A (ja) | 2014-10-30 |
MX2014002837A (es) | 2014-06-23 |
JP2017170613A (ja) | 2017-09-28 |
CN103781593A (zh) | 2014-05-07 |
BR112014005560A2 (pt) | 2017-04-04 |
CA2848294A1 (en) | 2013-03-21 |
CN103781593B (zh) | 2017-03-01 |
US20130065490A1 (en) | 2013-03-14 |
KR20140075712A (ko) | 2014-06-19 |
EP2755799A1 (en) | 2014-07-23 |
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