US20020174605A1 - Polishing compound for sheet metal coating - Google Patents
Polishing compound for sheet metal coating Download PDFInfo
- Publication number
- US20020174605A1 US20020174605A1 US10/154,792 US15479202A US2002174605A1 US 20020174605 A1 US20020174605 A1 US 20020174605A1 US 15479202 A US15479202 A US 15479202A US 2002174605 A1 US2002174605 A1 US 2002174605A1
- Authority
- US
- United States
- Prior art keywords
- sheet metal
- polishing
- metal coating
- ceramics
- polishing compound
- 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
Links
- 238000005498 polishing Methods 0.000 title claims abstract description 72
- 238000000576 coating method Methods 0.000 title claims abstract description 57
- 239000011248 coating agent Substances 0.000 title claims abstract description 53
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 53
- 239000002184 metal Substances 0.000 title claims abstract description 53
- 150000001875 compounds Chemical class 0.000 title claims abstract description 39
- 239000000919 ceramic Substances 0.000 claims abstract description 64
- 239000000463 material Substances 0.000 claims abstract description 46
- 239000000843 powder Substances 0.000 claims abstract description 31
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 239000002245 particle Substances 0.000 claims description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- 239000003599 detergent Substances 0.000 claims description 15
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 8
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- 239000011230 binding agent Substances 0.000 claims description 7
- 239000000377 silicon dioxide Substances 0.000 claims description 7
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 6
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 6
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical compound [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 claims description 6
- 229910001942 caesium oxide Inorganic materials 0.000 claims description 6
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 6
- 239000000292 calcium oxide Substances 0.000 claims description 6
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 6
- 229910003460 diamond Inorganic materials 0.000 claims description 6
- 239000010432 diamond Substances 0.000 claims description 6
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims description 6
- 229910021332 silicide Inorganic materials 0.000 claims description 6
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 claims description 6
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 claims description 6
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 6
- 229910001930 tungsten oxide Inorganic materials 0.000 claims description 6
- 239000005909 Kieselgur Substances 0.000 claims description 4
- 239000002280 amphoteric surfactant Substances 0.000 claims description 4
- 239000003093 cationic surfactant Substances 0.000 claims description 4
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000008262 pumice Substances 0.000 claims description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 3
- 229920003169 water-soluble polymer Polymers 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 10
- 238000005406 washing Methods 0.000 abstract description 8
- 238000004904 shortening Methods 0.000 abstract 1
- 208000036357 GUCY2D-related recessive retinopathy Diseases 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 241000209094 Oryza Species 0.000 description 12
- 235000007164 Oryza sativa Nutrition 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- 235000009566 rice Nutrition 0.000 description 12
- -1 fatty acid salt Chemical class 0.000 description 10
- 229920003023 plastic Polymers 0.000 description 10
- 239000004033 plastic Substances 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 239000005011 phenolic resin Substances 0.000 description 7
- 239000010419 fine particle Substances 0.000 description 6
- 239000008240 homogeneous mixture Substances 0.000 description 6
- 239000012299 nitrogen atmosphere Substances 0.000 description 6
- 229920003987 resole Polymers 0.000 description 6
- 229920001187 thermosetting polymer Polymers 0.000 description 6
- KAKVFSYQVNHFBS-UHFFFAOYSA-N (5-hydroxycyclopenten-1-yl)-phenylmethanone Chemical compound OC1CCC=C1C(=O)C1=CC=CC=C1 KAKVFSYQVNHFBS-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- 238000007517 polishing process Methods 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000005539 carbonized material Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 229940105329 carboxymethylcellulose Drugs 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 239000013527 degreasing agent Substances 0.000 description 2
- 238000005237 degreasing agent Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 230000017525 heat dissipation Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- SBRWJSVZWFZLBG-UHFFFAOYSA-N 2-(dimethylamino)pentanoic acid;dodecanamide Chemical compound CCCC(N(C)C)C(O)=O.CCCCCCCCCCCC(N)=O SBRWJSVZWFZLBG-UHFFFAOYSA-N 0.000 description 1
- XPALGXXLALUMLE-UHFFFAOYSA-N 2-(dimethylamino)tetradecanoic acid Chemical compound CCCCCCCCCCCCC(N(C)C)C(O)=O XPALGXXLALUMLE-UHFFFAOYSA-N 0.000 description 1
- GWEBEJYKXBMRJL-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.OCCN(CCO)CCO.CCCCCCCCCCCCOCCCCCCCCCCCC GWEBEJYKXBMRJL-UHFFFAOYSA-N 0.000 description 1
- RZRILSWMGXWSJY-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;sulfuric acid Chemical compound OS(O)(=O)=O.OCCN(CCO)CCO RZRILSWMGXWSJY-UHFFFAOYSA-N 0.000 description 1
- MSHRLZROIXIQJV-UHFFFAOYSA-N 2-methyl-2-(propylamino)propanoic acid Chemical compound CCCNC(C)(C)C(O)=O MSHRLZROIXIQJV-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 1
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- YVIGPQSYEAOLAD-UHFFFAOYSA-L disodium;dodecyl phosphate Chemical compound [Na+].[Na+].CCCCCCCCCCCCOP([O-])([O-])=O YVIGPQSYEAOLAD-UHFFFAOYSA-L 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- JEMLSRUODAIULV-UHFFFAOYSA-M potassium;2-[dodecanoyl(methyl)amino]acetate Chemical compound [K+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O JEMLSRUODAIULV-UHFFFAOYSA-M 0.000 description 1
- PYJBVGYZXWPIKK-UHFFFAOYSA-M potassium;tetradecanoate Chemical compound [K+].CCCCCCCCCCCCCC([O-])=O PYJBVGYZXWPIKK-UHFFFAOYSA-M 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940075560 sodium lauryl sulfoacetate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- LFUXMTKAILZVTA-ZOWNYOTGSA-M sodium;(2s)-2-(dodecanoylamino)propanoate Chemical compound [Na+].CCCCCCCCCCCC(=O)N[C@@H](C)C([O-])=O LFUXMTKAILZVTA-ZOWNYOTGSA-M 0.000 description 1
- CAVXVRQDZKMZDB-UHFFFAOYSA-M sodium;2-[dodecanoyl(methyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O CAVXVRQDZKMZDB-UHFFFAOYSA-M 0.000 description 1
- UAJTZZNRJCKXJN-UHFFFAOYSA-M sodium;2-dodecoxy-2-oxoethanesulfonate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)CS([O-])(=O)=O UAJTZZNRJCKXJN-UHFFFAOYSA-M 0.000 description 1
- PLQISZLZPSPBDP-UHFFFAOYSA-M sodium;pentadecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCS([O-])(=O)=O PLQISZLZPSPBDP-UHFFFAOYSA-M 0.000 description 1
- RUTSRVMUIGMTHJ-UHFFFAOYSA-M sodium;tetradec-1-ene-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCC=CS([O-])(=O)=O RUTSRVMUIGMTHJ-UHFFFAOYSA-M 0.000 description 1
- AYFACLKQYVTXNS-UHFFFAOYSA-M sodium;tetradecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCCS([O-])(=O)=O AYFACLKQYVTXNS-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1454—Abrasive powders, suspensions and pastes for polishing
- C09K3/1463—Aqueous liquid suspensions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/14—Anti-slip materials; Abrasives
- C09K3/1409—Abrasive particles per se
Definitions
- This invention relates to a polishing compound for sheet metal coating and more particularly relates to a polishing compound for sheet metal coating for removing stains on a coated surface and simultaneously washing the surface in reparative sheet metal coating work of cars, etc. and other similar operation.
- the inventors have eagerly investigated and found that the above mentioned problem can be solved by using RB ceramics and/or CRB ceramics at least partially as an polishing material for a polishing compound for sheet metal coating and further formulating the ceramics in a detergent.
- the present invention has been developed on the basis of this fact.
- RB ceramics used in the present powder detergent is a powder of RB ceramics or CRB ceramics formed by grinding these ceramics to particles of 1 to 1000 ⁇ m.
- Each material of RB ceramics and CRB ceramics used in the present invention is prepared by the following manner.
- the above mentioned literature describes a method for preparing a carbon material or so-called RB ceramics by mixing and kneading a defatted product of rice bran and a thermosetting resin, press-molding the mixture to form a molded material, drying and then baking the dried material in an atmosphere of inert gas.
- Defatted rice bran used in the present invention is not limited to a specific species of rice and may either be a product of Japan or foreign countries.
- thermosetting resin used herein may also be any resin which can be thermally set and typically includes phenol-, diarylphthalate-, unsaturated polyester-, epoxy-, polyimide- and triazine resins, although a phenol resin is preferably used.
- thermoplastic resin such as polyamide may also be used together without departing from a scope of the present invention.
- a mixing ratio of the defatted rice bran to the thermosetting resin is in the range of 50 to 90:50 to 10 and preferably 70 to 80:30 to 20 in by weight.
- CRB ceramics used in the present invention is an improved material of RB ceramics obtained from defatted rice bran and a thermosetting resin.
- the defatted product of rice bran and the thermosetting resin are mixed and kneaded, primarily baked in an inert gas at 700 to 1,000° C. and ground to form a carbonated powder of about 60 mesh or less.
- the powder is then mixed and kneaded with the thermosetting resin , press-molded at a pressure of 20 to 30 Mpa and heat-treated again in an atmosphere of inert gas at 100 to 1,100° C. to form CRB ceramics as a black resin or porous product.
- Hardness is an important factor of RB ceramics and/or CRB ceramics used in the present invention, which is influenced by the primary baking temperature of RB ceramics and both of the primary baking temperature and the secondary heat-treating temperature of CRB ceramics.
- the primary baking and the secondary heat treatment at a temperature of 500 to 1,000° C. yield RB ceramics or CRB ceramics of high hardness.
- Particle size of a RB ceramics or CRB ceramics powder may vary depending on the purpose to be used but usually in the range of 1 to 1,000 ⁇ m in average particle diameter, although, in general, a powder of a larger particle diameter is applied to a coarse surface and smaller one to a smooth surface.
- polishing materials which may be used in combination with RB ceramics and/or CRB ceramics in the present invention include diatomaceous earth, pumice powder, alumina, silica, calcium oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride, titanium oxide and the like.
- diatomaceous earth and pumice powder as a natural polishing material; or an alumina polishing material such brown-, white-, pale red- and crushed type alumina polishing material, and a silicon carbide grinding material such as black- and green silicon carbide grinding material as a synthetic one.
- alumina polishing material such brown-, white-, pale red- and crushed type alumina polishing material
- silicon carbide grinding material such as black- and green silicon carbide grinding material as a synthetic one.
- a combining ratio of these materials may vary depending on the purpose to be used and, in general, 30 to 90 parts by weight of a RB ceramics and/or CRB ceramics powder is combined with 70 to 10 parts by weight of one or not less than two kinds of powders selected from a group consisting of silica, calcium oxide, aluminum oxide, silicon nitride, silicon carbide, cesium oxide, natural or synthetic diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide.
- a detergent used in the present invention is selected from annionic surfactant, amphoteric surfactant, nonionic_surfactant or_cationic surfactant and the like.
- the anionic surfactant includes, for example, a fatty acid salt such as potassium laurate, potassium myristate and potassium oleate; an alkyl sulfate such as sodium laurylsulfate, ammonium laurylsulfate andlauryl sulfate triethanolamine; alkylbenzene-sulfonate such as sodium dodecylbenzenesulfonate; a N-acylamino acid salt such as lauroylsarcosine sodium salt and lauroylsarcosine potassium salt; an alkyl ether carbonate such as polyoxyethylene dodecyl ether sodium acetate; a N-acyl taurine salt such as N-lauroyl-methyltaurine sodium salt and N-cocoylmethyltaurine sodium salt; a N-acylalnine salt such as lauroylalanine sodium salt; a sulfonate such as sodium laurylsulfoacetate; polyoxy
- the amphoteric surfactant includes, for example, an acetic acid betain type surfactant such as lauryldimethylaminoacetic acid betain, lauric acid amide propyl-dimethylaminoacetic acid betain and coconut oil fatty acid amide propyldimethyl-aminoacetic acid betain; and an imidazoline type surfactant such as N-coconut oil fatty acid acyl-N-carboxymethyl-N-hydroxyethylenediamine sodium salt.
- an acetic acid betain type surfactant such as lauryldimethylaminoacetic acid betain, lauric acid amide propyl-dimethylaminoacetic acid betain and coconut oil fatty acid amide propyldimethyl-aminoacetic acid betain
- an imidazoline type surfactant such as N-coconut oil fatty acid acyl-N-carboxymethyl-N-hydroxyethylenediamine sodium salt.
- the nonionic surfactant includes, for example, a polyoxyethylene alkyl ether such as polyoxyethylene lauryl ether; and an alkyl alkanolamide.
- the cationic surfactant includes, for example, an alkylammonium salt such as lauryltrimethylammonium chloride; and an lauryldimethylamine oxide.
- An amount of the detergent to be added is preferably 1 to 30 parts by weight per 100 parts by weight of the polishing material.
- An amount thereof less than 1 part by weight results in too weak detergency to wash out wax and dirt from hands sufficiently, while the amount of more than 30 parts by weight lowers rinsing efficiency and is not preferable from an economical viewpoint.
- the detergent may either be used alone or in combination of two or more.
- the present polishing compound for sheet metal coating may be compounded by mixing an polishing material and a surfactant in the following two manners.
- a polishing material is dispersed in an aqueous solution of detergent to form a polishing compound for sheet metal coating of adequate viscosity in a state of paste or liquid depending on an amount of water to be added to the detergent.
- the polishing material and the detergent are thoroughly mixed by shaking a container containing the compound sufficiently to apply by means of rag or other waste cloth soaked therewith.
- a detergent and a powdery polishing material are mixed and solidified with a binder.
- the compound is soaked in a solvent such as water which dissolves the binder, and applied to a surface to be coated by scoring thereon, thereby the coated surface being abraded and washed.
- a binder used in the present invention includes carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), starch, alcohol soluble polyamide, etc.
- CMC carboxymethyl cellulose
- PVA polyvinyl alcohol
- starch alcohol soluble polyamide
- PVA polyvinyl alcohol
- starch are a water soluble high polymer and preferably used in the present invention.
- a polishing compound for sheet metal coating comprising a polishing material and a detergent in which a RB ceramics and/or CRB ceramics powder is used at least as a part of the polishing material.
- an polishing material is one or not less than two kinds of powders selected from a group consisting of diatomaceous earth, pumice powder, alumina, silica, calcium oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide.
- a polishing compound for sheet metal coating described in the above item 2 in which an polishing material comprises a RB ceramics and/or CRB ceramics powder and one or not less than two kinds of powders selected from a group consisting of silica, calcium oxide, aluminum oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide, in a weight ratio of 30 to 90:70 to 10, respectively.
- the present invention provides a polishing compound for sheet metal coating in reparative sheet metal coating work of cars, which shortens a stain removing process of a coated surface without conducting a cleaning process thereafter in reparative sheet metal coating work of cars, etc. by using an environmentally acceptable material of RB ceramics and/or CRB ceramics as an polishing material.
- RB ceramics and/or CRB ceramics is a black material, its residue on the abraded surface is quite noticeable, if any, and is useful as an indicator of surface washing with water.
- a defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- the mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 60 minutes.
- the thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 ⁇ m in particle diameter.
- the carbonized powder in an amount of 75 kg and a solid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 100 to 150° C. to form a plastic and homogeneous mixture.
- the plastic mixture was press-molded at a pressure of 20 Mpa to form a spherical body of 3 cm in diameter.
- the mold die temperature was 150° C.
- the thus molded body was taken out of the mold die and subjected to a heat treatment by heating-up to 500° C. in a nitrogen atmosphere at a heat rising rate of 1° C. per minute, keeping at 500° C. for 60 minutes and then baking 900° C. for 120 minutes.
- the molded body was then cooled at a cool down rate of 2 to 3° C. per minute down to at 500° C., followed by natural heat dissipation under 500° C.
- the spherical body of 3 cm in diameter was ground by a grinder and further pulverized by a ball mill to form CRB ceramics primary particles of 5 to 10 ⁇ m in average particle diameter.
- the slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated.
- the flawed surface was smoothened, the surface was washed with water and dried.
- a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- a defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- the mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 60 minutes.
- the thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 ⁇ m in particle diameter.
- the plastic mixture was press-molded at a pressure of 20 Mpa to form a spherical body of 3 cm in diameter.
- the mold die temperature was 150° C.
- the thus molded body was taken out of the mold die and subjected to a heat treatment by heating-up to 500° C. in a nitrogen atmosphere at a heat rising rate of 1° C. per minute, keeping at 500° C. for 60 minutes and then baking 850° C. for 120 minutes.
- the molded body was then cooled at a cool down rate of 2 to 3° C. per minute down to at 500° C., followed by natural heat dissipation under 500° C.
- the spherical body of 3 cm in diameter was ground by a grinder and then screened through a 300-mesh screen to form CRB ceramics primary particles of 50 to 80 ⁇ m in average particle diameter.
- the slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated.
- the flawed surface was smoothened, the surface was washed with water and dried.
- a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- a defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- the mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 80 minutes.
- the thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 ⁇ m in particle diameter.
- the carbonized powder was further pulverized by a ball mill to form RB ceramics primary fine particles of 30 to 40 ⁇ m in average particle diameter.
- the slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated.
- the flawed surface was smoothened, the surface was washed with water and dried.
- a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- a defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- the mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 70 minutes.
- the thus baked material was screened through a 60-mesh screen to obtain a carbonized powder of 200 to 400 ⁇ m in particle diameter, which was further pulverized by means of a ball mill to form primary fine particles of RB ceramics having an average particle diameter of 100 to 200 ⁇ m.
- the molded polishing compound for sheet metal coating was brought to an polishing and washing site and soaked with water to directly and carefully rub a rusted and flawed car surface to be coated. As a result, the rust was completely removed. When the flawed surface was smoothened, the surface was washed with water and dried. After confirming the absence of oil film on the surface, a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
Abstract
There is provided a polishing compound for sheet metal coating comprising an polishing material and a surfactant in which a RB ceramics and/or CRB ceramics powder is used at least as a part of the polishing material, thereby shortening a stain removing process of a coated surface in reparative sheet metal coating work of cars, etc. without conducting a washing process thereafter.
Description
- This invention relates to a polishing compound for sheet metal coating and more particularly relates to a polishing compound for sheet metal coating for removing stains on a coated surface and simultaneously washing the surface in reparative sheet metal coating work of cars, etc. and other similar operation.
- Conventional reparative sheet metal coating work of cars, etc. is carried out by removing stains with polishing materials such as polishing grains, paper, etc. and then washing and degreasing a coated surface by means of toweling, cotton cloth and other rags saturated with a degreasing agent, followed by face coating.
- However, it has been imperfect and taken a long time for these conventional polishing materials to abrade the surface and sometimes difficult to wash out wax or oily dirt from hands completely, although stains of ordinary dirt or dust can be removed.
- Such wax or oily dirt from hands still sticks on the coated surface even after a stain removing process with conventional polishing materials and thus should be washed out additionally.
- Inferiority in adhesion, scaling, peeling, blister and the like would be resulted in after coating, if the above mentioned additional wash-out process is neglected. This is the reason why the conventional stain removing work takes a long time including the indispensable process to wash out and degrease the coated surface with a degreasing agent after the polishing process is finished, which causes a problem of lowering efficiency in the reparative sheet metal coating work.
- Accordingly, it is an object of the present invention to provide a polishing compound for sheet metal coating in reparative sheet metal coating work of cars, etc., which shortens a stain removing process of a coated surface without conducting a wash-out process thereafter.
- The inventors have eagerly investigated and found that the above mentioned problem can be solved by using RB ceramics and/or CRB ceramics at least partially as an polishing material for a polishing compound for sheet metal coating and further formulating the ceramics in a detergent. The present invention has been developed on the basis of this fact.
- RB ceramics used in the present powder detergent is a powder of RB ceramics or CRB ceramics formed by grinding these ceramics to particles of 1 to 1000 μm.
- Each material of RB ceramics and CRB ceramics used in the present invention is prepared by the following manner.
- As is known, Dr. Kazuo Hokkirigawa, the first inventor of the present invention, proposed an idea to obtain a porous carbon material by the use of rice bran which is by-produced 0.9 million ton/year in Japan or 33 million ton/year in the world (see, Kinou Zairyou, Vol. 17, No. 5, pp. 24 to 28, May 1997).
- The above mentioned literature describes a method for preparing a carbon material or so-called RB ceramics by mixing and kneading a defatted product of rice bran and a thermosetting resin, press-molding the mixture to form a molded material, drying and then baking the dried material in an atmosphere of inert gas.
- Defatted rice bran used in the present invention is not limited to a specific species of rice and may either be a product of Japan or foreign countries.
- A thermosetting resin used herein may also be any resin which can be thermally set and typically includes phenol-, diarylphthalate-, unsaturated polyester-, epoxy-, polyimide- and triazine resins, although a phenol resin is preferably used.
- A thermoplastic resin such as polyamide may also be used together without departing from a scope of the present invention.
- A mixing ratio of the defatted rice bran to the thermosetting resin is in the range of 50 to 90:50 to 10 and preferably 70 to 80:30 to 20 in by weight.
- According to the above mentioned method, difference in ratio of shrinkage between the press-molded material and the finally molded material which is baked in an atmosphere of inert gas reached almost 25%. Such a difference made it substantially difficult to form a precisely molded material, but has been finally improved as a result of development of CRB ceramics.
- CRB ceramics used in the present invention is an improved material of RB ceramics obtained from defatted rice bran and a thermosetting resin. The defatted product of rice bran and the thermosetting resin are mixed and kneaded, primarily baked in an inert gas at 700 to 1,000° C. and ground to form a carbonated powder of about 60 mesh or less. The powder is then mixed and kneaded with the thermosetting resin , press-molded at a pressure of 20 to 30 Mpa and heat-treated again in an atmosphere of inert gas at 100 to 1,100° C. to form CRB ceramics as a black resin or porous product.
- General properties of RB ceramics and CRB ceramics are as in the following:
- extremely high hardness;
- oil absorptive;
- extremely small heat expansion coefficient;
- porous structure;
- electrical conductivity;
- low specific gravity, light weighted;
- improved abrasion resistance;
- easiness of molding and mold die making;
- capable of being powdered; and
- less negative effect to global environment and more resource conservation due to rice bran to be used a s a starting material.
- The most typical distinction of RB ceramics and CRB ceramics is that a difference in ratio of shrinkage between molded RB ceramics and a final product thereof is almost 25%, while that of CRB ceramics is so low as 3% or less, which makes the latter material much useful. However, such distinction between them is not important in the present invention, because the final product is formed not as a molded material but as a powder. So, either of RB ceramics or CRB ceramics may basically be used in the present invention.
- Hardness is an important factor of RB ceramics and/or CRB ceramics used in the present invention, which is influenced by the primary baking temperature of RB ceramics and both of the primary baking temperature and the secondary heat-treating temperature of CRB ceramics.
- In general, the primary baking and the secondary heat treatment at a temperature of 500 to 1,000° C. yield RB ceramics or CRB ceramics of high hardness.
- Particle size of a RB ceramics or CRB ceramics powder may vary depending on the purpose to be used but usually in the range of 1 to 1,000 μm in average particle diameter, although, in general, a powder of a larger particle diameter is applied to a coarse surface and smaller one to a smooth surface.
- Well-known polishing materials which may be used in combination with RB ceramics and/or CRB ceramics in the present invention include diatomaceous earth, pumice powder, alumina, silica, calcium oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride, titanium oxide and the like.
- It is preferable to use diatomaceous earth and pumice powder as a natural polishing material; or an alumina polishing material such brown-, white-, pale red- and crushed type alumina polishing material, and a silicon carbide grinding material such as black- and green silicon carbide grinding material as a synthetic one. These polishing or grinding materials may be used alone or in combination with two or more of them.
- A combining ratio of these materials may vary depending on the purpose to be used and, in general, 30 to 90 parts by weight of a RB ceramics and/or CRB ceramics powder is combined with 70 to 10 parts by weight of one or not less than two kinds of powders selected from a group consisting of silica, calcium oxide, aluminum oxide, silicon nitride, silicon carbide, cesium oxide, natural or synthetic diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide.
- A detergent used in the present invention is selected from annionic surfactant, amphoteric surfactant, nonionic_surfactant or_cationic surfactant and the like.
- The anionic surfactant includes, for example, a fatty acid salt such as potassium laurate, potassium myristate and potassium oleate; an alkyl sulfate such as sodium laurylsulfate, ammonium laurylsulfate andlauryl sulfate triethanolamine; alkylbenzene-sulfonate such as sodium dodecylbenzenesulfonate; a N-acylamino acid salt such as lauroylsarcosine sodium salt and lauroylsarcosine potassium salt; an alkyl ether carbonate such as polyoxyethylene dodecyl ether sodium acetate; a N-acyl taurine salt such as N-lauroyl-methyltaurine sodium salt and N-cocoylmethyltaurine sodium salt; a N-acylalnine salt such as lauroylalanine sodium salt; a sulfonate such as sodium laurylsulfoacetate; polyoxyethylene alkyl ether sulfuric acid ester salt such as sodium polyoxyethylene lauryl ether sulfate and poloyoxyethylene lauryl ether sulfuric acid triethanolamine; an alkanesulfonate such as sodium tetradecanesulfonate and sodium pentadecanesulfonate; an α-olefinic sulfonate such as sodium tetradecenesulfonate; an alkylphosphate such as sodium laurylphosphate; a polyoxyethylene lauryl ether phosphate such as sodium polyoxyethylene lauryl ether phosphate and the like.
- The amphoteric surfactant includes, for example, an acetic acid betain type surfactant such as lauryldimethylaminoacetic acid betain, lauric acid amide propyl-dimethylaminoacetic acid betain and coconut oil fatty acid amide propyldimethyl-aminoacetic acid betain; and an imidazoline type surfactant such as N-coconut oil fatty acid acyl-N-carboxymethyl-N-hydroxyethylenediamine sodium salt.
- The nonionic surfactant includes, for example, a polyoxyethylene alkyl ether such as polyoxyethylene lauryl ether; and an alkyl alkanolamide.
- The cationic surfactant includes, for example, an alkylammonium salt such as lauryltrimethylammonium chloride; and an lauryldimethylamine oxide.
- An amount of the detergent to be added is preferably 1 to 30 parts by weight per 100 parts by weight of the polishing material.
- An amount thereof less than 1 part by weight results in too weak detergency to wash out wax and dirt from hands sufficiently, while the amount of more than 30 parts by weight lowers rinsing efficiency and is not preferable from an economical viewpoint.
- The detergent may either be used alone or in combination of two or more.
- The present polishing compound for sheet metal coating may be compounded by mixing an polishing material and a surfactant in the following two manners.
- In one type, a polishing material is dispersed in an aqueous solution of detergent to form a polishing compound for sheet metal coating of adequate viscosity in a state of paste or liquid depending on an amount of water to be added to the detergent. When the liquid or pasty polishing compound for sheet metal coating is used in practice, the polishing material and the detergent are thoroughly mixed by shaking a container containing the compound sufficiently to apply by means of rag or other waste cloth soaked therewith.
- In the other type, a detergent and a powdery polishing material are mixed and solidified with a binder. When the thus formed solid compound is used in practice, the compound is soaked in a solvent such as water which dissolves the binder, and applied to a surface to be coated by scoring thereon, thereby the coated surface being abraded and washed.
- A binder used in the present invention includes carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA), starch, alcohol soluble polyamide, etc. In particular, carboxy-methyl cellulose (CMC), polyvinyl alcohol (PVA) and starch are a water soluble high polymer and preferably used in the present invention.
- The present invention will be summarized as in the following.
- 1. A polishing compound for sheet metal coating comprising a polishing material and a detergent in which a RB ceramics and/or CRB ceramics powder is used at least as a part of the polishing material.
- 2. A polishing compound for sheet metal coating described in the above item 1 in which an polishing material is one or not less than two kinds of powders selected from a group consisting of diatomaceous earth, pumice powder, alumina, silica, calcium oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide.
- 3. A polishing compound for sheet metal coating described in the above item 2 in which an polishing material comprises a RB ceramics and/or CRB ceramics powder and one or not less than two kinds of powders selected from a group consisting of silica, calcium oxide, aluminum oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide, in a weight ratio of 30 to 90:70 to 10, respectively.
- 4. A polishing compound for sheet metal coating described in any one of the above items 1 to 3 in which an average particle diameter of RB ceramics and/or CRB ceramics powder is 1 to 300 μm.
- 5. A polishing compound for sheet metal coating described in any one of the above items 1 to 4 in which a detergent is one or not less than two surfactants selected from a group consisting of an anionic surfactant, amphoteric surfactant, nonionic surfactant or cationic surfactant.
- 6. A polishing compound for sheet metal coating described in any one of the above items 1 to 5 in which an polishing material and a detergent are solidified with a binder.
- 7. A polishing compound for sheet metal coating described in the above item 6 in which a binder is a water soluble polymer.
- As has been described above, the present invention provides a polishing compound for sheet metal coating in reparative sheet metal coating work of cars, which shortens a stain removing process of a coated surface without conducting a cleaning process thereafter in reparative sheet metal coating work of cars, etc. by using an environmentally acceptable material of RB ceramics and/or CRB ceramics as an polishing material.
- Further, as RB ceramics and/or CRB ceramics is a black material, its residue on the abraded surface is quite noticeable, if any, and is useful as an indicator of surface washing with water.
- The present invention will be further described by the following examples.
- Preparation of CRB ceramics
- A defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- The mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 60 minutes. The thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 μm in particle diameter.
- The carbonized powder in an amount of 75 kg and a solid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 100 to 150° C. to form a plastic and homogeneous mixture.
- Preparation of polishing material
- Then, the plastic mixture was press-molded at a pressure of 20 Mpa to form a spherical body of 3 cm in diameter. The mold die temperature was 150° C.
- The thus molded body was taken out of the mold die and subjected to a heat treatment by heating-up to 500° C. in a nitrogen atmosphere at a heat rising rate of 1° C. per minute, keeping at 500° C. for 60 minutes and then baking 900° C. for 120 minutes.
- The molded body was then cooled at a cool down rate of 2 to 3° C. per minute down to at 500° C., followed by natural heat dissipation under 500° C.
- The spherical body of 3 cm in diameter was ground by a grinder and further pulverized by a ball mill to form CRB ceramics primary particles of 5 to 10 μm in average particle diameter.
- Preparation of polishing compound for sheet metal coating
- Primary fine particles of CRB ceramics having an average particle diameter of 5 μm in an amount of 2 kg, 2.5 kg of water and 0.5 kg of potassium laurate were mixed at room temperature and further treated by means of a roll mill to yield a homogeneously slurried polishing compound for sheet metal coating.
- Polishing process and coating
- The slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated. When the flawed surface was smoothened, the surface was washed with water and dried. After confirming the absence of oil film on the surface, a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- Preparation of CRB ceramics
- A defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- The mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 60 minutes. The thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 μm in particle diameter.
- The carbonized powder in an amount of 75 kg and a solid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 100 to 150° C. to form a plastic and homogeneous mixture.
- Preparation of polishing material
- Then, the plastic mixture was press-molded at a pressure of 20 Mpa to form a spherical body of 3 cm in diameter. The mold die temperature was 150° C.
- The thus molded body was taken out of the mold die and subjected to a heat treatment by heating-up to 500° C. in a nitrogen atmosphere at a heat rising rate of 1° C. per minute, keeping at 500° C. for 60 minutes and then baking 850° C. for 120 minutes.
- The molded body was then cooled at a cool down rate of 2 to 3° C. per minute down to at 500° C., followed by natural heat dissipation under 500° C.
- The spherical body of 3 cm in diameter was ground by a grinder and then screened through a 300-mesh screen to form CRB ceramics primary particles of 50 to 80 μm in average particle diameter.
- Preparation of polishing compound for sheet metal coating
- Primary fine particles of CRB ceramics having an average particle diameter of 70 μm in an amount of 2 kg, 0.5 kg of powdery silica having an average particle diameter of 10 μm, 2.5 kg of water and 0.5 kg of potassium laurate were mixed at room temperature while further stirring to yield a homogeneously slurried polishing compound for sheet metal coating.
- Polishing process and coating
- The slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated. When the flawed surface was smoothened, the surface was washed with water and dried. After confirming the absence of oil film on the surface, a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- Preparation of RB ceramics
- A defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- The mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 80 minutes. The thus baked and carbonized material was screened through a 100-mesh screen to obtain a carbonized powder of 50 to 250 μm in particle diameter.
- Preparation of polishing material
- The carbonized powder was further pulverized by a ball mill to form RB ceramics primary fine particles of 30 to 40 μm in average particle diameter.
- Preparation of polishing compound for sheet metal coating
- Primary fine particles of RB ceramics having an average particle diameter of 30 μm in an amount of 2 kg, 1 kg of powdery alumina having an average particle diameter of 5 μm, 3.0 kg of water and 0.5 kg of potassium laurate as an anionic surfactant were mixed at room temperature and further treated by means of a roll mill to yield a homogeneously slurried polishing compound for sheet metal coating.
- Polishing process and coating
- The slurried polishing compound for sheet metal coating was brought to an polishing and washing site and impregnated into rags to carefully rub a flawed car surface to be coated. When the flawed surface was smoothened, the surface was washed with water and dried. After confirming the absence of oil film on the surface, a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
- Preparation of RB ceramics
- A defatted product of rice bran in an amount of 75 kg and a liquid phenol resin (resol) in an amount of 25 kg were mixed and kneaded by heating at 50 to 60° C. to form a plastic and homogeneous mixture.
- Preparation of polishing material
- The mixture was primarily baked by means of a rotary kiln in a nitrogen atmosphere at 900° C. for 70 minutes. The thus baked material was screened through a 60-mesh screen to obtain a carbonized powder of 200 to 400 μm in particle diameter, which was further pulverized by means of a ball mill to form primary fine particles of RB ceramics having an average particle diameter of 100 to 200 μm.
- Preparation of polishing compound for sheet metal coating
- Primary fine particles of RB ceramics having an average particle diameter of 150 μm in an amount of 2 kg, 1 kg of powdery alumina having an average particle diameter of 5 μm, 1.5 kg of water and 0.5 kg of potassium laurate as an anionic surfactant were mixed at room temperature and further added with 0.5 kg of carboxymethyl cellulose (CMC) to form a plastic composition. The plastic composition was molded into a cylindrical body of 3 cm in diameter and 15 cm in height, which was dried to form a molded polishing compound for sheet metal coating.
- Polishing process and coating
- The molded polishing compound for sheet metal coating was brought to an polishing and washing site and soaked with water to directly and carefully rub a rusted and flawed car surface to be coated. As a result, the rust was completely removed. When the flawed surface was smoothened, the surface was washed with water and dried. After confirming the absence of oil film on the surface, a commercially available paint was sprayed thereon several times to the sheet metal coating. Inferior in adhesion, scaling, peeling, blister and other defects were not observed after the coating process.
Claims (7)
1. A polishing compound for sheet metal coating comprising an polishing material and a detergent in which a RB ceramics and/or CRB ceramics powder is used at least as a part of the polishing material.
2. A polishing compound for sheet metal coating claimed in claim 1 in which an polishing material is one or not less than two kinds of powders selected from a group consisting of diatomaceous earth, pumice powder, alumina, silica, calcium oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide.
3. A polishing compound for sheet metal coating claimed in claim 2 in which an polishing material comprises a RB ceramics and/or CRB ceramics powder and one or not less than two kinds of powders selected from a group consisting of silica, calcium oxide, aluminum oxide, silicon nitride, silicon carbide, cesium oxide, synthetic or natural diamond, metal silicide, tungsten oxide, titanium nitride and titanium oxide, in a weight ratio of 30 to 90:70 to 10, respectively.
4. A polishing compound for sheet metal coating claimed in any one of claims 1 to 3 in which an average particle diameter of RB ceramics and/or CRB ceramics powder is 1 to 1,000 μm.
5. A polishing compound for sheet metal coating claimed in any one of claims 1 to 4 in which a detergent is one or not less than two surfactants selected from a group consisting of an anionic-, amphoteric surfactant, nonionic surfactant and cationic surfactant.
6. A polishing compound for sheet metal coating claimed in any one of claims 1 to 5 in which an polishing material and a detergent are solidified with a binder.
7. A polishing compound for sheet metal coating claimed in claim 6 in which a binder is a water soluble polymer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001-157523 | 2001-05-25 | ||
| JP2001157523A JP2002348562A (en) | 2001-05-25 | 2001-05-25 | Compound for coating sheet metal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| US20020174605A1 true US20020174605A1 (en) | 2002-11-28 |
| US6494928B1 US6494928B1 (en) | 2002-12-17 |
Family
ID=19001370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/154,792 Expired - Fee Related US6494928B1 (en) | 2001-05-25 | 2002-05-24 | Polishing compound for sheet metal coating |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US6494928B1 (en) |
| JP (1) | JP2002348562A (en) |
| CN (1) | CN1235986C (en) |
| AU (1) | AU783398B2 (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030179963A1 (en) * | 2002-03-01 | 2003-09-25 | Minebea Co., Ltd. | Low friction sleeve bearing |
| EP1369202A1 (en) * | 2002-06-05 | 2003-12-10 | Minebea Co. Ltd. | Superfinishing grindstone |
| US20040031642A1 (en) * | 2002-06-05 | 2004-02-19 | Kazuo Hokkirigawa | Air purifying sound insulating wall and its applications |
| US20040132881A1 (en) * | 2003-01-07 | 2004-07-08 | Minebea Co., Ltd. | Oil repelling agent |
| US20040258334A1 (en) * | 2003-02-28 | 2004-12-23 | Minebea Co., Ltd. | Underwater sleeve bearing and application thereof |
| US6846355B2 (en) | 2002-06-19 | 2005-01-25 | Minebea Co., Ltd. | Road paving material and method |
| US7008196B2 (en) | 2003-03-11 | 2006-03-07 | Minebea Co. Ltd. | Electrically motorized pump having a submersible sleeve bearing |
| US20110064687A1 (en) * | 2007-06-12 | 2011-03-17 | Rhodia Inc. | Mono-, di- and polyol phosphate esters in personal care formulations |
| US20110172136A1 (en) * | 2007-06-12 | 2011-07-14 | Rhodia Operations | Detergent composition with hydrophilizing soil-release agent and methods for using same |
| US20110177012A1 (en) * | 2007-06-12 | 2011-07-21 | Rhodia Inc. | Mono-, di- and polyol alkoxylate phosphate esters in oral care formulations and methods for using same |
| EP2152845A4 (en) * | 2007-06-12 | 2012-01-25 | Rhodia | HARD SURFACE CLEANING COMPOSITION WITH HYDROPHILIZATION AGENT AND METHOD FOR CLEANING HARD SURFACES |
| US8993506B2 (en) | 2006-06-12 | 2015-03-31 | Rhodia Operations | Hydrophilized substrate and method for hydrophilizing a hydrophobic surface of a substrate |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002317196A (en) * | 2001-04-19 | 2002-10-31 | Minebea Co Ltd | Abrasive cleaning composition |
| US20030210995A1 (en) * | 2002-03-13 | 2003-11-13 | Minebea Co., Ltd. | Electrically motorized pump for use in water |
| JP4430984B2 (en) * | 2004-05-25 | 2010-03-10 | Hoya株式会社 | Imaging unit, camera body and camera system |
| GB0612788D0 (en) * | 2006-06-28 | 2006-08-09 | Insectshield Ltd | Pest control materials |
| TW200945429A (en) * | 2008-04-24 | 2009-11-01 | Uwiz Technology Co Ltd | Composition of chemical mechanical polishing |
| CN101818028A (en) * | 2009-10-20 | 2010-09-01 | 浙江超微细化工有限公司 | Process method for preparing aluminum trioxide-based polishing powder by solid-solid phase synthesis |
| US8840961B1 (en) | 2011-06-30 | 2014-09-23 | Salvatore Lucca | Composition and method for cleaning and lubricating valves and slides within musical instruments |
-
2001
- 2001-05-25 JP JP2001157523A patent/JP2002348562A/en active Pending
-
2002
- 2002-05-24 US US10/154,792 patent/US6494928B1/en not_active Expired - Fee Related
- 2002-05-24 AU AU44378/02A patent/AU783398B2/en not_active Ceased
- 2002-05-27 CN CNB02121915XA patent/CN1235986C/en not_active Expired - Fee Related
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030220421A1 (en) * | 2002-03-01 | 2003-11-27 | Minebea, Co., Ltd. | Low noise synthetic resin composition and method |
| US20030179963A1 (en) * | 2002-03-01 | 2003-09-25 | Minebea Co., Ltd. | Low friction sleeve bearing |
| US7140778B2 (en) | 2002-03-01 | 2006-11-28 | Minebea Co., Ltd. | Synthetic resin composites and bearings formed therefrom and method |
| US6887288B2 (en) * | 2002-06-05 | 2005-05-03 | Minebea Co., Ltd. | Superfinishing grindstone |
| EP1369202A1 (en) * | 2002-06-05 | 2003-12-10 | Minebea Co. Ltd. | Superfinishing grindstone |
| US20040033766A1 (en) * | 2002-06-05 | 2004-02-19 | Kazuo Hokkirigawa | Superfinishing grindstone |
| US20040031642A1 (en) * | 2002-06-05 | 2004-02-19 | Kazuo Hokkirigawa | Air purifying sound insulating wall and its applications |
| US6846355B2 (en) | 2002-06-19 | 2005-01-25 | Minebea Co., Ltd. | Road paving material and method |
| US20040132881A1 (en) * | 2003-01-07 | 2004-07-08 | Minebea Co., Ltd. | Oil repelling agent |
| US7160622B2 (en) | 2003-01-07 | 2007-01-09 | Minebea Co., Ltd. | Oil repelling agent |
| US20040258334A1 (en) * | 2003-02-28 | 2004-12-23 | Minebea Co., Ltd. | Underwater sleeve bearing and application thereof |
| US7008196B2 (en) | 2003-03-11 | 2006-03-07 | Minebea Co. Ltd. | Electrically motorized pump having a submersible sleeve bearing |
| US8993506B2 (en) | 2006-06-12 | 2015-03-31 | Rhodia Operations | Hydrophilized substrate and method for hydrophilizing a hydrophobic surface of a substrate |
| US20110064687A1 (en) * | 2007-06-12 | 2011-03-17 | Rhodia Inc. | Mono-, di- and polyol phosphate esters in personal care formulations |
| US20110172136A1 (en) * | 2007-06-12 | 2011-07-14 | Rhodia Operations | Detergent composition with hydrophilizing soil-release agent and methods for using same |
| US20110177012A1 (en) * | 2007-06-12 | 2011-07-21 | Rhodia Inc. | Mono-, di- and polyol alkoxylate phosphate esters in oral care formulations and methods for using same |
| EP2152845A4 (en) * | 2007-06-12 | 2012-01-25 | Rhodia | HARD SURFACE CLEANING COMPOSITION WITH HYDROPHILIZATION AGENT AND METHOD FOR CLEANING HARD SURFACES |
| US8263049B2 (en) | 2007-06-12 | 2012-09-11 | Rhodia Operations. | Mono-, di- and polyol alkoxylate phosphate esters in oral care formulations and methods for using same |
| US8263542B2 (en) | 2007-06-12 | 2012-09-11 | Rhodia Operations | Detergent composition with an organophosphorus hydrophilizing soil-release agent and methods for using same |
| US8268765B2 (en) | 2007-06-12 | 2012-09-18 | Rhodia Operations | Mono-, di- and polyol phosphate esters in personal care formulations |
| US8293699B2 (en) | 2007-06-12 | 2012-10-23 | Rhodia Operations | Hard surface cleaning composition with hydrophilizing agent and method for cleaning hard surfaces |
Also Published As
| Publication number | Publication date |
|---|---|
| AU4437802A (en) | 2002-11-28 |
| CN1388187A (en) | 2003-01-01 |
| JP2002348562A (en) | 2002-12-04 |
| US6494928B1 (en) | 2002-12-17 |
| AU783398B2 (en) | 2005-10-20 |
| CN1235986C (en) | 2006-01-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6494928B1 (en) | Polishing compound for sheet metal coating | |
| US3808747A (en) | Mechanical finishing and media therefor | |
| EP0628382A1 (en) | Plastic flexible grinding stone | |
| US4591363A (en) | Process of making a coated abrasive for diamond grinding wheels | |
| CA1096741A (en) | Scouring cleansers | |
| US5277708A (en) | Buffing composition | |
| US6673762B2 (en) | Contaminated surface polishing-washing detergent composition | |
| JP3590906B2 (en) | Compound for barrel polishing and barrel polishing method | |
| JPH10130633A (en) | Polisher for stainless steel | |
| CN110982638A (en) | Preparation process of foam cleaning agent | |
| US6783433B2 (en) | Polishing-washing method | |
| US6670318B2 (en) | Liquid cleanser | |
| US3944499A (en) | Non-aqueous cleaning composition | |
| RU2035499C1 (en) | Agent for solid surface cleansing | |
| TWI693282B (en) | Automobile glass cleaner and preparation method thereof | |
| US2041744A (en) | Pulverulent cleaning composition | |
| JP2813241B2 (en) | Abrasive and manufacturing method thereof | |
| JPH06330089A (en) | Compound for coating sheet metal | |
| US2322066A (en) | Polish and process of making it | |
| US1025946A (en) | Polishing compound. | |
| RU96111755A (en) | ABRASIVE MICROPOWER FOR POLISHING ON THE BASIS OF ALUMINUM OXIDES AND 3D METAL AND A METHOD FOR ITS OBTAINING | |
| JP2004299044A (en) | Offset-type flexible grinding wheel comprising resinoid bonding agent and its manufacturing method | |
| US20030087589A1 (en) | Foamed glass and ground glass surface or object treating agent, use therefor, and method of making same | |
| JPH0853697A (en) | Powder detergent | |
| JPH0830183B2 (en) | Metal abrasive |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: MINEBEA CO., LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HOKKIRIGAWA, KAZUO;AKIYAMA, MOTOHARU;YOSHIMURA, NORIYUKI;REEL/FRAME:012940/0194;SIGNING DATES FROM 20020426 TO 20020508 |
|
| REMI | Maintenance fee reminder mailed | ||
| LAPS | Lapse for failure to pay maintenance fees | ||
| STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
| FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20061217 |