CA1284987C - Compositions lubrifiantes - Google Patents

Compositions lubrifiantes

Info

Publication number: CA1284987C
Authority: CA; Canada
Prior art keywords: bis; composition according; tert; formula; propan
Prior art date: 1986-03-22
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.): Expired - Lifetime

Application number

CA000532575A

Other languages

English (en)

Inventor

Robert M. O'neil

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Ciba Geigy Investments Ltd

Original Assignee

Ciba Geigy AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-03-22

Filing date

1987-03-20

Publication date

1991-06-18

1987-03-20 Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG

1991-06-18 Application granted granted Critical

1991-06-18 Publication of CA1284987C publication Critical patent/CA1284987C/fr

2008-06-18 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 53
230000001050 lubricating effect Effects 0.000 title abstract description 3
239000003963 antioxidant agent Substances 0.000 claims abstract description 10
230000007797 corrosion Effects 0.000 claims abstract description 10
238000005260 corrosion Methods 0.000 claims abstract description 10
239000000654 additive Substances 0.000 claims abstract description 9
230000003078 antioxidant effect Effects 0.000 claims abstract description 9
239000003112 inhibitor Substances 0.000 claims abstract description 8
239000006078 metal deactivator Substances 0.000 claims abstract description 8
230000000996 additive effect Effects 0.000 claims abstract description 7
239000002530 phenolic antioxidant Substances 0.000 claims abstract description 7
125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 6
239000010687 lubricating oil Substances 0.000 claims abstract description 5
230000001590 oxidative effect Effects 0.000 claims abstract description 5
150000001875 compounds Chemical class 0.000 claims description 20
-1 octyl diphenylamines Chemical class 0.000 claims description 18
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 7
125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 7
239000012141 concentrate Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 5
UVEXVMUTHAZSNB-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]dodecan-2-ol Chemical group CCCCCCCCCCC(O)CN(CCO)CCO UVEXVMUTHAZSNB-UHFFFAOYSA-N 0.000 claims description 3
DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical group CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 claims description 3
AVBBHCMDRGQBNW-UHFFFAOYSA-N 2-ethyl-n-(2-ethylhexyl)-n-(1,2,4-triazol-1-ylmethyl)hexan-1-amine Chemical group CCCCC(CC)CN(CC(CC)CCCC)CN1C=NC=N1 AVBBHCMDRGQBNW-UHFFFAOYSA-N 0.000 claims description 3
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 claims description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
239000011701 zinc Substances 0.000 claims description 3
229910052725 zinc Inorganic materials 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
239000012442 inert solvent Substances 0.000 claims description 2
125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 claims description 2
239000003350 kerosene Substances 0.000 claims description 2
229940059904 light mineral oil Drugs 0.000 claims description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
239000010688 mineral lubricating oil Substances 0.000 claims description 2
229910052760 oxygen Inorganic materials 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
235000006708 antioxidants Nutrition 0.000 claims 4
IQYDSMJRFWLGKA-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]-3-(4-nonylphenoxy)propan-2-ol Chemical compound CCCCCCCCCC1=CC=C(OCC(O)CN(CCO)CCO)C=C1 IQYDSMJRFWLGKA-UHFFFAOYSA-N 0.000 claims 1
JFPNAUDFJSIIQV-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]-3-[2,4-di(propan-2-yl)phenoxy]propan-2-ol Chemical compound CC(C)C1=CC=C(OCC(O)CN(CCO)CCO)C(C(C)C)=C1 JFPNAUDFJSIIQV-UHFFFAOYSA-N 0.000 claims 1
229910019142 PO4 Inorganic materials 0.000 claims 1
230000002401 inhibitory effect Effects 0.000 claims 1
OKQVTLCUHATGDD-UHFFFAOYSA-N n-(benzotriazol-1-ylmethyl)-2-ethyl-n-(2-ethylhexyl)hexan-1-amine Chemical compound C1=CC=C2N(CN(CC(CC)CCCC)CC(CC)CCCC)N=NC2=C1 OKQVTLCUHATGDD-UHFFFAOYSA-N 0.000 claims 1
239000010452 phosphate Substances 0.000 claims 1
125000005504 styryl group Chemical group 0.000 claims 1
239000000047 product Substances 0.000 description 9
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
239000003921 oil Substances 0.000 description 7
235000019198 oils Nutrition 0.000 description 7
239000000314 lubricant Substances 0.000 description 6
150000001412 amines Chemical class 0.000 description 5
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
238000000034 method Methods 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
229940035422 diphenylamine Drugs 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000010802 sludge Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
LUKIFOVSRKGAMG-UHFFFAOYSA-N 1-[bis(2-hydroxyethyl)amino]-3-(6-methylheptoxy)propan-2-ol Chemical compound CC(C)CCCCCOCC(O)CN(CCO)CCO LUKIFOVSRKGAMG-UHFFFAOYSA-N 0.000 description 2
LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
239000005864 Sulphur Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
BJFLSHMHTPAZHO-UHFFFAOYSA-N benzotriazole Chemical compound [CH]1C=CC=C2N=NN=C21 BJFLSHMHTPAZHO-UHFFFAOYSA-N 0.000 description 2
239000012964 benzotriazole Substances 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
239000011707 mineral Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
229920000193 polymethacrylate Polymers 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
XBJHHKYUHTWRKV-UHFFFAOYSA-N 2-(nonylsulfanylmethyl)oxirane Chemical group CCCCCCCCCSCC1CO1 XBJHHKYUHTWRKV-UHFFFAOYSA-N 0.000 description 1
LCWDWRKWLVEBSS-UHFFFAOYSA-N 2-[6-methylheptoxy-[6-methylheptoxy(oxiran-2-yl)methoxy]methyl]oxirane Chemical compound C(CCCCC(C)C)OC(C1CO1)OC(C1CO1)OCCCCCC(C)C LCWDWRKWLVEBSS-UHFFFAOYSA-N 0.000 description 1
MPGABYXKKCLIRW-UHFFFAOYSA-N 2-decyloxirane Chemical compound CCCCCCCCCCC1CO1 MPGABYXKKCLIRW-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
VCOONNWIINSFBA-UHFFFAOYSA-N 4-methoxy-n-(4-methoxyphenyl)aniline Chemical compound C1=CC(OC)=CC=C1NC1=CC=C(OC)C=C1 VCOONNWIINSFBA-UHFFFAOYSA-N 0.000 description 1
SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 1
125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
239000005069 Extreme pressure additive Substances 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
XOFNJOHYONGGHB-UHFFFAOYSA-N N1=CNC2=C1C=CC=C2.N2N=CN=C2 Chemical compound N1=CNC2=C1C=CC=C2.N2N=CN=C2 XOFNJOHYONGGHB-UHFFFAOYSA-N 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000007866 anti-wear additive Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
JYZIHLWOWKMNNX-UHFFFAOYSA-N benzimidazole Chemical compound C1=C[CH]C2=NC=NC2=C1 JYZIHLWOWKMNNX-UHFFFAOYSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000012043 crude product Substances 0.000 description 1
125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
125000005266 diarylamine group Chemical group 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
125000005066 dodecenyl group Chemical group C(=CCCCCCCCCCC)* 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
125000004356 hydroxy functional group Chemical group O* 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000463 material Substances 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004370 n-butenyl group Chemical group [H]\C([H])=C(/[H])C([H])([H])C([H])([H])* 0.000 description 1
CVVFFUKULYKOJR-UHFFFAOYSA-N n-phenyl-4-propan-2-yloxyaniline Chemical compound C1=CC(OC(C)C)=CC=C1NC1=CC=CC=C1 CVVFFUKULYKOJR-UHFFFAOYSA-N 0.000 description 1
150000004950 naphthalene Chemical class 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000005187 nonenyl group Chemical group C(=CCCCCCCC)* 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
239000003444 phase transfer catalyst Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229920001083 polybutene Polymers 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000010736 steam turbine oil Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000005063 tetradecenyl group Chemical group C(=CCCCCCCCCCCCC)* 0.000 description 1
125000005040 tridecenyl group Chemical group C(=CCCCCCCCCCCC)* 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010723 turbine oil Substances 0.000 description 1
125000005065 undecenyl group Chemical group C(=CCCCCCCCCC)* 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
- 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
- C10M129/10—Hydroxy compounds having hydroxy groups bound to a carbon atom of a six-membered aromatic ring
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M133/08—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups
- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/043—Ammonium or amine salts thereof
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/12—Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Chemistry (AREA)
Lubricants (AREA)

CA000532575A 1986-03-22 1987-03-20 Compositions lubrifiantes Expired - Lifetime CA1284987C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB8607157		1986-03-22
GB868607157A GB8607157D0 (en)	1986-03-22	1986-03-22	Lubricating compositions

Publications (1)

Publication Number	Publication Date
CA1284987C true CA1284987C (fr)	1991-06-18

Family

ID=10595078

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000532575A Expired - Lifetime CA1284987C (fr)	1986-03-22	1987-03-20	Compositions lubrifiantes

Country Status (5)

Country	Link
EP (1)	EP0239536B1 (fr)
JP (1)	JPS62270697A (fr)
CA (1)	CA1284987C (fr)
DE (1)	DE3779942D1 (fr)
GB (1)	GB8607157D0 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH01188592A (ja) *	1988-01-22	1989-07-27	Matsushita Electric Ind Co Ltd	流体軸受用潤滑油
US5273669A (en) *	1988-07-18	1993-12-28	Ciba-Geigy Corporation	Lubricant composition
US5073278A (en) *	1988-07-18	1991-12-17	Ciba-Geigy Corporation	Lubricant composition
JPH0742468B2 (ja) *	1989-06-16	1995-05-10	コスモ石油株式会社	タービン油組成物
EP0432089B1 (fr) *	1989-11-08	1996-09-04	Ciba-Geigy Ag	Compositions lubrifiantes
EP0437416A3 (en) *	1990-01-11	1991-12-18	Ciba-Geigy Ag	Compositions containing a 2,2',2"-nitrilotriethanol-cyclometallate
US5344454A (en) *	1991-07-24	1994-09-06	Baxter International Inc.	Closed porous chambers for implanting tissue in a host
FR2679246A1 (fr) *	1991-07-15	1993-01-22	Exxon France	Composition d'huile et son utilisation comme isolant electrique.
US6773458B1 (en)	1991-07-24	2004-08-10	Baxter International Inc.	Angiogenic tissue implant systems and methods
DE69324746T2 (de) *	1992-09-02	1999-10-21	The Lubrizol Corp., Wickliffe	Antioxidanten für hoch einfach-ungesättigte pflanzliche Öle
US5670464A (en) *	1993-01-25	1997-09-23	Kao Corporation	Additive for lubricating oils for diesel engines and lubricating oil compositions containing the same
WO2006136591A1 (fr) *	2005-06-23	2006-12-28	Shell Internationale Research Maatschappij B.V.	Formulation d'huile oxydative stable
US20080139421A1 (en) *	2006-12-06	2008-06-12	Loper John T	Lubricating Composition
JP6776495B2 (ja)	2015-03-20	2020-10-28	出光興産株式会社	潤滑油組成物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2856363A (en) *	1955-12-01	1958-10-14	Pure Oil Co	Stable anti-rust lubricating oil
US4298481A (en) *	1979-02-23	1981-11-03	Tenneco Chemicals, Inc.	High temperature grease compositions
EP0045827B1 (fr) *	1980-08-12	1983-11-02	Mobil Oil Corporation	Compositions lubrifiantes contenant des mélanges de triazoles et de thiadiazoles comme antioxydants
GB2172284B (en) *	1985-03-12	1988-07-27	Ciba Geigy Ag	Nitrogen-containing additives for non-aqueous functional fluids
DE3688011D1 (de) *	1985-06-21	1993-04-22	Ciba Geigy Ag	Schmiermittelzusammensetzungen, neue glucamin-derivate und diese enthaltende komplexverbindungen.

1986
- 1986-03-22 GB GB868607157A patent/GB8607157D0/en active Pending
1987
- 1987-03-16 DE DE8787810152T patent/DE3779942D1/de not_active Expired - Lifetime
- 1987-03-16 EP EP87810152A patent/EP0239536B1/fr not_active Expired - Lifetime
- 1987-03-20 JP JP62067733A patent/JPS62270697A/ja active Pending
- 1987-03-20 CA CA000532575A patent/CA1284987C/fr not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0239536A3 (en)	1989-07-26
JPS62270697A (ja)	1987-11-25
DE3779942D1 (de)	1992-07-30
EP0239536B1 (fr)	1992-06-24
EP0239536A2 (fr)	1987-09-30
GB8607157D0 (en)	1986-04-30

Legal Events

Date	Code	Title	Description
1993-12-20	MKLA	Lapsed

Publication	Publication Date	Title
US7704931B2 (en)	2010-04-27	Lubricant compositions stabilized with multiple antioxidants
US7829511B2 (en)	2010-11-09	Stabilized lubricant compositions
US7928045B2 (en)	2011-04-19	Stabilizing compositions for lubricants
US5531911A (en)	1996-07-02	Metal free hydraulic fluid with amine salt
EP0160620A2 (fr)	1985-11-06	Désactivateurs de métaux
JP2021501245A (ja)	2021-01-14	酸化防止剤高分子ジフェニルアミン組成物
EP0239536B1 (fr)	1992-06-24	Compositions lubrifiantes
EP0273868B1 (fr)	1992-07-08	Tétrahydroquinoléines N-substituées comme anti-oxydants pour lubrifiants
JP2008512534A (ja)	2008-04-24	アルキルアミノアセトアミド潤滑油添加剤
US4946612A (en)	1990-08-07	Lubricating oil composition for sliding surface and for metallic working and method for lubrication of machine tools using said composition
JPH0762148B2 (ja)	1995-07-05	機能油組成物
US4102797A (en)	1978-07-25	Compounds containing both urea and urethane groups
DE69007214T2 (de)	1994-07-14	Butenylaromatische Aminstabilisatoren.
EP0741736A1 (fr)	1996-11-13	Additifs anti-usure et leur utilisation
RU2680133C1 (ru)	2019-02-18	Улучшенные антиоксидантные композиции и содержащие их смазочные композиции
EP0682022B1 (fr)	2002-07-24	Produits de condensation de mélamine, de benzotriazoles et d'aldéhydes
JPH06206887A (ja)	1994-07-26	トリスアミドジチオノジフォスフェート
EP0595771A1 (fr)	1994-05-04	Additifs pour lubrifiants exempts de phosphore
EP0323403A2 (fr)	1989-07-05	Composition lubrifiante
US20240336865A1 (en)	2024-10-10	Novel additive mixture
EP0595770A1 (fr)	1994-05-04	Nouveaux dithiophosphates comme additifs anti-usure
JPH07179874A (ja)	1995-07-18	炭化水素油添加剤及びそれを含む潤滑油組成物