KR900006496A - 수성매질에 분산시킨 희토류 할로겐화물의 분산액 - Google Patents
수성매질에 분산시킨 희토류 할로겐화물의 분산액 Download PDFInfo
- Publication number
- KR900006496A KR900006496A KR1019890014526A KR890014526A KR900006496A KR 900006496 A KR900006496 A KR 900006496A KR 1019890014526 A KR1019890014526 A KR 1019890014526A KR 890014526 A KR890014526 A KR 890014526A KR 900006496 A KR900006496 A KR 900006496A
- Authority
- KR
- South Korea
- Prior art keywords
- rare earth
- acid
- dispersion
- radical
- earth halides
- Prior art date
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- -1 rare earth halides Chemical class 0.000 title claims 55
- 229910052761 rare earth metal Inorganic materials 0.000 title claims 45
- 239000006185 dispersion Substances 0.000 title claims 41
- 239000012736 aqueous medium Substances 0.000 title claims 4
- 229920001577 copolymer Polymers 0.000 claims 17
- 125000004432 carbon atom Chemical group C* 0.000 claims 16
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 16
- 239000002253 acid Substances 0.000 claims 11
- 229920000642 polymer Polymers 0.000 claims 10
- 239000002270 dispersing agent Substances 0.000 claims 9
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 7
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 claims 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 4
- 239000002518 antifoaming agent Substances 0.000 claims 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 4
- 239000001530 fumaric acid Substances 0.000 claims 4
- 229920002554 vinyl polymer Polymers 0.000 claims 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- 239000002585 base Substances 0.000 claims 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 3
- 239000011976 maleic acid Substances 0.000 claims 3
- 150000003460 sulfonic acids Chemical class 0.000 claims 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 3
- 239000004711 α-olefin Substances 0.000 claims 3
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 claims 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims 2
- SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 claims 2
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims 2
- WWUVJRULCWHUSA-UHFFFAOYSA-N 2-methyl-1-pentene Chemical compound CCCC(C)=C WWUVJRULCWHUSA-UHFFFAOYSA-N 0.000 claims 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 2
- 125000005907 alkyl ester group Chemical group 0.000 claims 2
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims 2
- 229940018557 citraconic acid Drugs 0.000 claims 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 2
- 150000005690 diesters Chemical class 0.000 claims 2
- 150000004820 halides Chemical class 0.000 claims 2
- 150000007529 inorganic bases Chemical class 0.000 claims 2
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims 2
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 claims 2
- 150000007530 organic bases Chemical class 0.000 claims 2
- 238000006116 polymerization reaction Methods 0.000 claims 2
- 229910052700 potassium Inorganic materials 0.000 claims 2
- 239000011591 potassium Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims 2
- AHAREKHAZNPPMI-AATRIKPKSA-N (3e)-hexa-1,3-diene Chemical compound CC\C=C\C=C AHAREKHAZNPPMI-AATRIKPKSA-N 0.000 claims 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 claims 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 claims 1
- SFJOBYZKUSLNIG-UHFFFAOYSA-N 2,3,4-tris(1-phenylethyl)phenol Chemical compound C=1C=C(O)C(C(C)C=2C=CC=CC=2)=C(C(C)C=2C=CC=CC=2)C=1C(C)C1=CC=CC=C1 SFJOBYZKUSLNIG-UHFFFAOYSA-N 0.000 claims 1
- ALEYBMUCCRAJEB-UHFFFAOYSA-N 2,3-bis(1-phenylethyl)phenol Chemical compound C=1C=CC(O)=C(C(C)C=2C=CC=CC=2)C=1C(C)C1=CC=CC=C1 ALEYBMUCCRAJEB-UHFFFAOYSA-N 0.000 claims 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical group NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 1
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 claims 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 claims 1
- RYKZRKKEYSRDNF-UHFFFAOYSA-N 3-methylidenepentane Chemical compound CCC(=C)CC RYKZRKKEYSRDNF-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- 229910052684 Cerium Inorganic materials 0.000 claims 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 claims 1
- 229910052779 Neodymium Inorganic materials 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 1
- 229910052777 Praseodymium Inorganic materials 0.000 claims 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims 1
- 229910052772 Samarium Inorganic materials 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
- 241000209140 Triticum Species 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000000908 ammonium hydroxide Substances 0.000 claims 1
- 150000003863 ammonium salts Chemical class 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 claims 1
- QCCDYNYSHILRDG-UHFFFAOYSA-K cerium(3+);trifluoride Chemical group [F-].[F-].[F-].[Ce+3] QCCDYNYSHILRDG-UHFFFAOYSA-K 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 238000007872 degassing Methods 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- 239000002612 dispersion medium Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 claims 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 239000003349 gelling agent Substances 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 229910052746 lanthanum Inorganic materials 0.000 claims 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims 1
- 239000000314 lubricant Substances 0.000 claims 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- 150000002989 phenols Chemical class 0.000 claims 1
- 235000021317 phosphate Nutrition 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 claims 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 claims 1
- 238000010298 pulverizing process Methods 0.000 claims 1
- 238000010526 radical polymerization reaction Methods 0.000 claims 1
- 150000002910 rare earth metals Chemical class 0.000 claims 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 125000004436 sodium atom Chemical group 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 claims 1
- 229920001567 vinyl ester resin Polymers 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/14—Derivatives of phosphoric acid
-
- 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
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/16—Amines or polyamines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M103/00—Lubricating compositions characterised by the base-material being an inorganic material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/04—Hydroxy compounds
- C10M129/06—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/08—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least 2 hydroxy groups
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/18—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/24—Polyethers
- C10M145/26—Polyoxyalkylenes
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/18—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/24—Polyethers
- C10M145/26—Polyoxyalkylenes
- C10M145/36—Polyoxyalkylenes etherified
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M149/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (38)
- (a) 에틸렌계 불포화 카르복실산 또는 그의 유도체와 α-올레핀 화합물 및/또는 비닐 화합물의 공중합체. (b) 에틸렌계 불포화 카르복실산 또는 그의 유도체의 단복 중합체 또는 공중합체. (c) 하나이상의 에틸렌계 불포화 카르복실산과 하나이상의 에틸렌계 불포화 술폰산염의 공중합체. (d) (아릴알킬) 페놀의 산화 알킬렌, 경우에 따라 그의 인산염 또는 황산염의 중합체로 이루어진 군중에서 선택되는 하나 이상의 분산체, 및 하나이상의 희토류 할로겐화물을 포함함을 특징으로 하는 수성매질 중의 희토류 할로겐화물을 포함함을 특징으로 하는 수성매질 중의 희토류 할로겐화물 분산액.
- 제1항에 있어서, 희토류 할로겐화물이 희토류 삼플루오르 화합물임을 특징으로 하는 할로겐화물의 분산액.
- 제1 또는 2항에 있어서. 희토류 할로겐화물이 세륨, 란탄, 프라세오디뮴, 네오디뮴 및/또는 사마륨임을 특징으로 하는 희토류 할로겐화물 분산액.
- 제1 내지 3항중 어느 한항에 있어서, 희토류 할로겐화물이 0.1 내지 0.5㎛의 결정립 평균직경을 나타내는 삼플루오르화 세륨임을 특징으로 하는 희토류 할로겐화물 분산액.
- 제1 내지 4항중 어느 한 항에 있어서, 분산제가 하기로 부터 수득된 공중합체(a)임을 특징으로 하는 희토류 할로겐화물 분산액.* 식(I)의 불포화 카르복실산 또는 그의 유도체중 하나,(식(I)중, -X는 수소원자, 또는 무기 또는 유기염기의 잔기를 나타내고, -Ra는 수소원자 경우에 따라 -COOX기를 보유하는 1내지 10개의 탄소원자를 갖는 알킬 라디칼이고, -Rb는 수소원자 또는 -COOX기이다)* 식(II)에 해당하는 α-올레핀 화합물 및/또는 식(III)의 비닐 화합물,(II);CH2 (III) 식(II) 및 (III)중, -RC는 수소원자 또는 1내지 4개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼을 나타내고, -Rd는 1내지 12개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼을 나타내고, -Re는 수소원자 또는 1내지 4개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼을 나타내고, -Rf는 하기의 기중 하나를 나타낸다.: Rg는 수소원자, 또는 1내지 4개의 탄소원자를 갖는 하나이상의 알킬 라디칼을 나타낸다.·Cl·OOC-Rh: Rh는 1내지 8개의 탄소원자를 갖는 알킬 라디칼이다.·O-Rj: Rj는 Rh와 동일한 의미를 갖는다.·COOX·COO-Rj는 Rh와 동일한 의미를 갖는다.·CO-NH2·C=N
- 제5항에 있어서, 공중합체(a)의 성분으로 사용되는 에틸렌계 불포화 카르복실산 또는 유도체가 말레산 또는 푸마르산 또는 에스테르, 헤미에스테르 같은 그의 유도체; 이타콘산, 시크라콘산; 말레산 무수물; 모노-및 디알킬 말레산, 밀 모노- 및 디알킬 푸마르산(알킬라디칼은 1 내지 4개의 탄소원자를 갖는다) 임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5 또는 6항에 있어서, 공중합체(a)의 성분으로 사용되는 α-올레핀 화합물이 에틸렌, 프로필렌, 1-부텐, 이소부틸렌, n-1-펜텐, 이소프렌, 2-메틸-1-부텐, n-1-헥센, 2-메틸-1-펜텐, 4-메틸-1-펜텐, 2-에틸-1-부텐, 2,4,4-트리메틸-1-펜텐(디이소부틸렌이라고 불림), 1,3-부라디엔, 1,3-펜타디엔, 1,3-헥사디엔, 1,3-옥타디엔, 2-메릴-3,3-디메틸-1-펜텐, 2-메틸-4,4-디메틸-1-펜텐임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5 내지 7항중 어느 한 항에 있어서, 공중합체(a)의 성분으로 사용되는 비닐 화합물이 스티렌, 염화비닐; 아세트산 비닐,프로피온산 비닐, 부티르산 비닐 같은 1내지 8개의 탄소원자를 가진 지방족산의 비닐 에스테르; 산화메틸 및 산화비닐 같은 비닐 에테르; 아크릴산 또는 메타크릴산 및 아크릴산 메틸, 아크릴산 에틸, 아크릴산 부틸, 메타크릴산 메틸, 메타크릴산 에틸, 메타크릴산 부틸 같은 1내지 8개의 탄소원자를 함유하는 알킬 에스테르, 아크릴아미도, 메타크릴아미도, 아크릴로니트릴, 메타크릴로니트릴 임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5항에 있어서, 공중합체(a)가 무수 말레산-디이소부틸렌 공중합체임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5 내지 9항중 어느 한 항에 있어서, 공중합체(a)가 500 내지 50,000의 중량 평균 분자량을 가짐을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제10항에 있어서, 공중합체(a)가 500 내지 15,000의 중량평균 분자량을 가짐을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5 내지 11항중 어느 한 항에 있어서, 식(I)의 카르복실산/식(II) 및/또는(III)의 불포화 화합물의 몰비가 1임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제5 내지 12항중 어느 한 항에 있어서, 공중합체(a)가 유기용매내에서 라디칼 중합에 의한 수득됨을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제13항에 있어서, 공중합체(a)가, pH 8내지 12로 수득될때까지 염기의 첨가에 의해 중화됨을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제1 내지 4항중 어느 한 항에 있어서, 분산제가 하기식(IV)에 해당하는 하나이상의 에틸렌계 불포화 카르복실산 도는 그의 유도체 중 하나를 중합시킨 중합체(b)임을 특징으로 하는 희토류 할로겐화물의 분산액.(식(IV)중, -R'는 수소원자, 염소원자 또는 경우에 따라 -COOX기를 보유하는 1내지 4개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼을 나타내고, -R"는 수소원자 또는 1내지 4개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼을 나타내고, -R"'은 수소원자, 1내지 4개의 탄소원자를 갖는 직쇄 또는 분지된 알킬 라디칼, 또는 -COOX기를 나타내고, -X는 상기 주어진 의미를 갖는다).
- 제15항에 있어서, 중합체(b)가 아크릴 또는 메타크릴산 및 메틸, 에틸 또는 부틸의 아크릴레이트 또는 메타크릴레이트, 에타크릴산, α-클로로아클리산, 크로톤산, 아타콘산, 말레산, 푸마르산, 시트라콘산, 메사콘산 등과 같은 1내지 4개의 탄소원자를 포함하는 그의 알킬 에스테르의 중합으로 부터 생성됨을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제16항에 있어서, 중합체(b)가 아크릴산 및/또는 메타크릴산의 중합으로 부터 생성됨을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제16 또는 17항에 있어서, 중합체(b)가 수산화나트륨, 수산화칼륨, 수산화 암모늄, 또는 수산화 알킬을 아민 같은 염기에 의해 처리됨을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제1 내지 4항중 어느 한 항에 있어서, 공중합체(c)의 성분으로 사용되는 에틸렌계 불포화 카르복실산의 아크릴산, 메타크릴산, 에타크릴산, α-클로로아크릴산, 크로톤산, 이타콘산, 말레산, 푸마르산, 시트라콘산, 메사콘산임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제19항에 있어서, 에틸렌계 불포화 카르복실산의 아크릴산 또는 메타크릴산임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제19항 또는 20항의 에틸렌계 불포화 카르복실산이 0.05/l 내지 10/l의 몰비에 따른 아크릴산 및 메타크릴산의 혼합물임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제21항에 있어서, 에틸렌계 불포화 카르복실산이 0.10/l 내지 6/l의 몰비에 따른 아크릴산 및 메타크릴산의 혼합물임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제19 내지 22항중 어느 한 항에 있어서, 공중합체(c)의 조성 내에 도입되는 에틸렌계 불포화 술폰산의 염기 알킬술폰산, 메탈릴술폰산, 비닐술폰산 또는 스티렌 술폰산의 알칼리 금속염 또는 암모늄염임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제23항에 있어서, 에틸렌계 불포화 술폰산의 염이 메탈릴술폰산 나트륨 또는 메탈릴 술폰산 칼륨임을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제19 내지 24항중 어느 한 항에 있어서, 에틸렌계 불포화 술폰산 염의 몰 백분율이 전체 모노머 혼합물의 1내지 60몰%를 나타냄을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제25항에 있어서, 상기 몰 백분율이 전체 모노리 혼합물의 3 내지 8몰%를 나타냄을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제19내지 26항중 어느 한 항에 있어서, 공중합체(c)가 500 내지 8,000의 중량 평균 분자량을 가짐을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제27항에 있어서, 공중합체(c)가 1,500 내지 4,000의 중량 평균 분자량을 가짐을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제1 내지 4항중 어느 한 항에 있어서, 분산제가 하기식(V) 내지 (VII)중 하나에 해당하는 중합체(d)임을 특징으로 하는 희토류 할로겐화물의 분산액.식(V)내지 식(VII)중, -n은 1내지 40이고, -X는 수소원자 또는 상기 정의한 것과 같은 무기 또는유기염기의 잔기이고, -R은 2내지 4개의 탄소원자를 갖는 알킬렌 라디칼이고, -R2는 잔기 X(R2=X일때, 두개의 잔기 X는 동일하거나 상이할 수 있다)이거나, R1-(O-R)-n 라디칼중 하나 (R2라디칼 및 R1-(O-R)-n 라디칼은 동일하거나 상이할 수 있다)이고, -R1식 (VIII)로 기호화된 라디칼을 나타낸다.식(VIII)중, m은 1,2 및 3의 정수이고, P는 1 또는 2의 정수이고, R4는 수소원자 또는 1내지 4개의 탄소원자를 갖는 알킬라디칼이고, R3라디칼은 하기식(IX)의 라디칼을 신호로 나타낸 것이다.식중, R5는 수소원자, 1내지 4개의 탄소원자를 갖는 알킬라디칼, 또는 페닐 라디칼을 나타낸다.
- 제29항에 있어서, 분산제가 하기 사항에 해당하는 식(V) 내지 (VII)중 하나인 중합체(d)임을 특징으로 하는 희토류 할로겐화물의 분산액.-R은 에틸렌 라디칼을 나타내고, -R1은 하기사항을 나타내는 식(VIII)의 라디칼을 나타내고, 식(VIII)중, m은 2 또는 3의 정수이고, R4는 수소원자이고, R3라디칼은 하기식(IX)의 라디칼이다.식중, R5는 수소원자, 메틸 또는 페닐 라디칼이다.-R2는 잔기 X(R2=X일때, 두개의 잔기 X는 동일하다)이거나, R1-(O-OH2-CH2)-n 라디칼 (R2라디칼 및 R1-(O-CH1-CH2)-n 라디칼은 동일하다)이다.
- 제29 또는 30항에 있어서, 분산제가 하기 사항에 해당하는 식(V) 내지 (VII)중 하나인 중합체(d)임을 특징으로 하는 희토류 할로겐화물의 분산액.-n은 3내지 40이고, -X는 수소원자, 나트륨원자, 칼륨원자, 암모늄라디칼, 모노에탈올아민, 디에탄올아민, 트리에탄올아민이고, -R은 에틸렌라디칼이고, -R1은 하기사항을 나타내는 식(VIII)의 라디칼을 나타내고, 식(VIII)중, m은 2 또는 3의 정수이고, R4는 수소원자이고, R3라디칼은 하기식(IX)의 라디칼이다.-R2는 잔기 X(R2=X일때, 두개의 잔기 X는 동일하다)이거나, R1-(O-OH2-CH2)-n 라디칼 (R2라디칼 및 R1-(O-CH1-CH2)-n 라디칼은 동일하다)이다.
- 제29내지 31항중 어느 한 항에 있어서, 분산제가 하기중에서 선택되는 중합체(d)임을 특징으로 하는 희토류 할로겐화물의 분산액.* 페놀몰당 10 내지 40몰의 산화 에틸렌(E.O.)을 갖는 트리-(1-페닐에틸)페놀폴리옥시에틸렌.* 페놀몰당 3 내지 20몰의 산화 에틸렌을 갖는 디-(1-페닐에틸)페놀폴리옥시에틸렌.* 페놀몰당 10 내지 40몰의 산화 에틸렌을 갖는, 산 또는 중화된 형의 트리-(1-페닐에틸)페놀폴리옥시에틸렌의 황산염.* 페놀몰당 3 내지 20몰의 산화 에틸렌을 갖는, 산 또는 중화된 형의 디-(1-페닐에틸)페놀 폴리옥시에틸렌의 황산염.* 페놀몰당 10 내지 40몰의 산 에틸렌을 갖는, 산화 또는 중화된 형의 트리-(1-페닐에틸)페놀 폴리옥시에틸렌 인산 모노- 및 디에스테르.* 페놀몰당 3 내지 20몰의 산 에틸렌을 갖는, 산화 또는 중화된 형의 디-(1-페닐에틸)페놀폴리옥시에틸렌의 인산 모노- 및 디에스테르.
- 제1 내지 32항중 어느 한항에 있어서, 겔화방지제 및/또는 발포방지제를 또한 포함함을 특징으로 하는 희토류 할로겐화물의 분산액.
- 제1 내지 33항중 어느 한 항에 있어서, 하기의 것을 포함함을 특징으로 하는 희토류 할로겐화물의 분산액.- 5내지 80%의 하나이상의 희토류 할로겐화물, - 0.1 내지 12%의 분산제(a),(b),(c) 및/또는 (d), - 0 내지 5%의 발포방지제, - 0 내지 20%의 겔화방지제, -100%를 수득하기 위한 충분량의 물.
- 제34항에 있어서, 하기의 것을 포함함을 특징으로 하는 희토류 할로겐화물의 분산액.- 20 내지 60%의 하나이상의 희토류 할로겐화물, - 0.4 내지 8%의 분산제(a),(b),(c) 및/또는 (d), - 0 내지 3%의 발포방지제, - 0 내지 15%의 겔화방지제, -100%를 수득하기 위한 충분량의 물.
- 분산제(a)(b)(c) 및 또는 (d), 경우에 따라 겔화방지제, 분산매질을 구성하는 물을 포함하는 용액을 제조하고, 하나이상의 회토류 할로겐화물을 교반하에서 분산시킨 후, 분산액을 분쇄하고, 경우에 따라 수득된 분산의 기체를 제거하는 것으로 구성됨을 특징으로 하는 제1 내지 35항중 어느 한항에 기재된 수성 매질중 희토류 할로겐화물 분산액의 제조방법.
- 제36항에 있어서, 발포방지제가 분쇄 과정중 또는 기체 제거시에 첨가됨을 특징으로 하는 방법.
- 윤활제 분야에서의, 제1 내지 35항중 한 항에 기재된 희토류 할로겐화물의 분산액의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
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FR8813263 | 1988-10-10 | ||
FR88/13263 | 1988-10-10 |
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KR900006496A true KR900006496A (ko) | 1990-05-08 |
KR930000653B1 KR930000653B1 (ko) | 1993-01-29 |
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US (1) | US4946607A (ko) |
EP (1) | EP0364328B1 (ko) |
JP (1) | JPH02164715A (ko) |
KR (1) | KR930000653B1 (ko) |
AT (1) | ATE77645T1 (ko) |
AU (1) | AU613798B2 (ko) |
BR (1) | BR8905084A (ko) |
DE (1) | DE68901909T2 (ko) |
FI (1) | FI894794A (ko) |
GR (1) | GR3005761T3 (ko) |
NO (1) | NO894000L (ko) |
ZA (1) | ZA897657B (ko) |
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GB2228274B (en) * | 1989-01-12 | 1992-01-02 | Sandoz Ltd | Surface active compositions their production and use |
FR2732620B1 (fr) * | 1995-04-10 | 1997-05-09 | Coatex Sa | Copolymeres utilises comme dispersant ameliorant la resistance a l'eau des films de compositions aqueuses chargees et/ou pigmentees ainsi que les compositions les contenant |
CN1058985C (zh) * | 1998-10-08 | 2000-11-29 | 中国科学院兰州化学物理研究所 | 纳米氟化稀土润滑油添加剂 |
CN1058984C (zh) * | 1998-10-08 | 2000-11-29 | 中国科学院兰州化学物理研究所 | 纳米氢氧化稀土润滑油添加剂 |
JP5532199B2 (ja) * | 2008-11-07 | 2014-06-25 | 株式会社豊田中央研究所 | 金属化合物のコロイド溶液およびその製造方法 |
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FR1279937A (fr) * | 1960-07-29 | 1961-12-29 | Cincinnati Milling Machine Co | Solution aqueuse de refroidissement, pour l'usinage de matières ferreuses |
DE1594511A1 (de) * | 1966-01-21 | 1970-12-17 | Dow Corning Gmbh | Gesenkschmierstoffe |
US3830280A (en) * | 1971-01-25 | 1974-08-20 | Mallory & Co Inc P R | Rare earth flouride lubricant for die casting components |
US4034133A (en) * | 1973-05-14 | 1977-07-05 | International Business Machines Corporation | Magnetic recording medium with lubricant |
JPS53129200A (en) * | 1977-04-18 | 1978-11-10 | Shiraishi Kogyo Kk | Dispersant for calcium carbonate |
FR2483932B1 (fr) * | 1980-06-09 | 1985-08-02 | Rhone Poulenc Spec Chim | Nouvelles compositions polymere acrylique, procede pour leur obtention, et application notamment comme agents antitartres |
US4507214A (en) * | 1983-11-02 | 1985-03-26 | Union Oil Company Of California | Rare earth halide grease compositions |
DE3508704A1 (de) * | 1985-03-12 | 1986-09-18 | Basf Ag, 6700 Ludwigshafen | Verwendung von copolymerisaten auf basis von alkyl (meth)-acrylaten als dispergiermittel fuer pigmente und waessrige pigmentanschlaemmungen |
FR2581323B1 (fr) * | 1985-05-06 | 1987-05-29 | Rhone Poulenc Spec Chim | Nouvelle composition tensio-active, son procede d'obtention et ses applications |
CH665847A5 (de) * | 1985-10-02 | 1988-06-15 | Lonza Ag | Verfahren zum suspendieren von festschmierstoffen. |
GB2193224A (en) * | 1986-05-27 | 1988-02-03 | Grace W R & Co | Fuel oil additives |
FR2601259B1 (fr) * | 1986-07-11 | 1990-06-22 | Rhone Poulenc Chimie | Nouvelles compositions tensio-actives a base d'esters phosphoriques leur procede de preparation et leur application a la formulation de matieres actives. |
-
1989
- 1989-10-02 DE DE8989402703T patent/DE68901909T2/de not_active Expired - Fee Related
- 1989-10-02 EP EP89402703A patent/EP0364328B1/fr not_active Expired - Lifetime
- 1989-10-02 AT AT89402703T patent/ATE77645T1/de not_active IP Right Cessation
- 1989-10-05 JP JP1258961A patent/JPH02164715A/ja active Pending
- 1989-10-06 BR BR898905084A patent/BR8905084A/pt unknown
- 1989-10-06 NO NO89894000A patent/NO894000L/no unknown
- 1989-10-09 AU AU42696/89A patent/AU613798B2/en not_active Ceased
- 1989-10-09 ZA ZA897657A patent/ZA897657B/xx unknown
- 1989-10-09 FI FI894794A patent/FI894794A/fi not_active IP Right Cessation
- 1989-10-10 US US07/419,218 patent/US4946607A/en not_active Expired - Fee Related
- 1989-10-10 KR KR1019890014526A patent/KR930000653B1/ko active IP Right Grant
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1992
- 1992-09-23 GR GR920402092T patent/GR3005761T3/el unknown
Also Published As
Publication number | Publication date |
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KR930000653B1 (ko) | 1993-01-29 |
NO894000D0 (no) | 1989-10-06 |
NO894000L (no) | 1990-04-11 |
FI894794A (fi) | 1990-04-11 |
EP0364328B1 (fr) | 1992-06-24 |
US4946607A (en) | 1990-08-07 |
EP0364328A2 (fr) | 1990-04-18 |
DE68901909D1 (de) | 1992-07-30 |
FI894794A0 (fi) | 1989-10-09 |
GR3005761T3 (ko) | 1993-06-07 |
ZA897657B (en) | 1990-07-25 |
DE68901909T2 (de) | 1993-02-04 |
EP0364328A3 (en) | 1990-07-04 |
JPH02164715A (ja) | 1990-06-25 |
AU4269689A (en) | 1990-04-12 |
BR8905084A (pt) | 1990-05-15 |
AU613798B2 (en) | 1991-08-08 |
ATE77645T1 (de) | 1992-07-15 |
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