NL8201722A - Antioxydatiemiddelcombinaties van molybdeencomplexen en aromatische amineverbindingen. - Google Patents

Antioxydatiemiddelcombinaties van molybdeencomplexen en aromatische amineverbindingen. Download PDF

Info

Publication number: NL8201722A
Authority: NL; Netherlands
Prior art keywords: carbon atoms; sulfur; molybdenum; additive according; compound
Prior art date: 1981-04-27

Application number

NL8201722A

Other languages

English (en)

Dutch (nl)

Original Assignee

Chevron Res

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.)

1981-04-27

Filing date

1982-04-26

Publication date

1982-11-16

1982-04-26 Application filed by Chevron Res filed Critical Chevron Res

1982-11-16 Publication of NL8201722A publication Critical patent/NL8201722A/nl

Links

-1 AROMATIC AMINE COMPOUNDS Chemical class 0.000 title claims description 53
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical class [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 title claims description 46
239000000203 mixture Substances 0.000 claims description 84
229910052757 nitrogen Inorganic materials 0.000 claims description 66
125000004432 carbon atom Chemical group C* 0.000 claims description 63
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 55
229910052717 sulfur Inorganic materials 0.000 claims description 53
239000011593 sulfur Substances 0.000 claims description 53
229910052750 molybdenum Inorganic materials 0.000 claims description 46
239000011733 molybdenum Substances 0.000 claims description 46
239000000654 additive Substances 0.000 claims description 41
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims description 41
239000004215 Carbon black (E152) Substances 0.000 claims description 36
229930195733 hydrocarbon Natural products 0.000 claims description 36
150000002430 hydrocarbons Chemical class 0.000 claims description 35
230000000996 additive effect Effects 0.000 claims description 28
125000000217 alkyl group Chemical group 0.000 claims description 28
239000010687 lubricating oil Substances 0.000 claims description 28
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 24
239000003921 oil Substances 0.000 claims description 24
239000005078 molybdenum compound Substances 0.000 claims description 21
150000002752 molybdenum compounds Chemical class 0.000 claims description 21
239000002253 acid Substances 0.000 claims description 18
238000006243 chemical reaction Methods 0.000 claims description 18
150000001875 compounds Chemical class 0.000 claims description 17
229910017464 nitrogen compound Inorganic materials 0.000 claims description 17
150000002830 nitrogen compounds Chemical class 0.000 claims description 17
229960002317 succinimide Drugs 0.000 claims description 17
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 15
125000004429 atom Chemical group 0.000 claims description 14
238000002360 preparation method Methods 0.000 claims description 14
230000002378 acidificating effect Effects 0.000 claims description 13
150000001412 amines Chemical class 0.000 claims description 13
125000003118 aryl group Chemical group 0.000 claims description 12
JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 claims description 12
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 12
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
229940014800 succinic anhydride Drugs 0.000 claims description 10
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 10
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 9
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 9
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 9
239000005077 polysulfide Substances 0.000 claims description 9
229920001021 polysulfide Polymers 0.000 claims description 9
150000008117 polysulfides Polymers 0.000 claims description 9
229960001124 trientine Drugs 0.000 claims description 9
125000002877 alkyl aryl group Chemical group 0.000 claims description 7
APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 claims description 7
229940010552 ammonium molybdate Drugs 0.000 claims description 7
235000018660 ammonium molybdate Nutrition 0.000 claims description 7
239000011609 ammonium molybdate Substances 0.000 claims description 7
125000000732 arylene group Chemical group 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
229920000768 polyamine Polymers 0.000 claims description 7
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims description 6
239000003963 antioxidant agent Substances 0.000 claims description 5
125000003710 aryl alkyl group Chemical group 0.000 claims description 5
229910052945 inorganic sulfide Inorganic materials 0.000 claims description 5
YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 claims description 5
DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 5
CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 claims description 4
150000004982 aromatic amines Chemical class 0.000 claims description 4
239000002270 dispersing agent Substances 0.000 claims description 4
150000003464 sulfur compounds Chemical class 0.000 claims description 4
XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 claims description 3
125000005541 phosphonamide group Chemical group 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 2
QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 claims description 2
230000003078 antioxidant effect Effects 0.000 claims description 2
DMSZORWOGDLWGN-UHFFFAOYSA-N ctk1a3526 Chemical compound NP(N)(N)=O DMSZORWOGDLWGN-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims 2
230000001050 lubricating effect Effects 0.000 claims 2
240000007124 Brassica oleracea Species 0.000 claims 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 claims 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 claims 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 claims 1
230000015572 biosynthetic process Effects 0.000 claims 1
150000001735 carboxylic acids Chemical class 0.000 claims 1
239000000428 dust Substances 0.000 claims 1
NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 claims 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
235000019198 oils Nutrition 0.000 description 21
239000000047 product Substances 0.000 description 18
238000012360 testing method Methods 0.000 description 16
150000001336 alkenes Chemical class 0.000 description 11
230000003647 oxidation Effects 0.000 description 11
238000007254 oxidation reaction Methods 0.000 description 11
239000011541 reaction mixture Substances 0.000 description 11
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 9
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 9
229910052760 oxygen Inorganic materials 0.000 description 9
239000001301 oxygen Substances 0.000 description 9
239000005909 Kieselgur Substances 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
239000003085 diluting agent Substances 0.000 description 8
150000002751 molybdenum Chemical class 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
238000009472 formulation Methods 0.000 description 7
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 7
238000010992 reflux Methods 0.000 description 7
239000000243 solution Substances 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000012141 concentrate Substances 0.000 description 6
RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-N 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 5
239000011575 calcium Substances 0.000 description 5
238000001816 cooling Methods 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
239000000314 lubricant Substances 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 4
239000005977 Ethylene Substances 0.000 description 4
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
229910052796 boron Inorganic materials 0.000 description 4
235000014113 dietary fatty acids Nutrition 0.000 description 4
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 4
239000000194 fatty acid Substances 0.000 description 4
229930195729 fatty acid Natural products 0.000 description 4
238000000034 method Methods 0.000 description 4
CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 4
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 4
JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
229910052791 calcium Inorganic materials 0.000 description 3
239000002826 coolant Substances 0.000 description 3
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 3
PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
239000002904 solvent Substances 0.000 description 3
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 2
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001335 aliphatic alkanes Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000003973 alkyl amines Chemical class 0.000 description 2
239000000908 ammonium hydroxide Substances 0.000 description 2
YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
239000002199 base oil Substances 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
150000001733 carboxylic acid esters Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
229910052802 copper Inorganic materials 0.000 description 2
239000010949 copper Substances 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 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
239000003925 fat Substances 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
238000001914 filtration Methods 0.000 description 2
230000009969 flowable effect Effects 0.000 description 2
239000000446 fuel Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
230000006698 induction Effects 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
229910052742 iron Inorganic materials 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000011777 magnesium Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
NCEGDHPVRKYIJN-UHFFFAOYSA-N n-pentyl-n-phenylnaphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(CCCCC)C1=CC=CC=C1 NCEGDHPVRKYIJN-UHFFFAOYSA-N 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
150000008039 phosphoramides Chemical class 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
229920000193 polymethacrylate Polymers 0.000 description 2
239000002243 precursor Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
150000003335 secondary amines Chemical class 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000001384 succinic acid Substances 0.000 description 2
150000004763 sulfides Chemical class 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 0.000 description 2
DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
WONYVCKUEUULQN-UHFFFAOYSA-N 2-methyl-n-(2-methylphenyl)aniline Chemical compound CC1=CC=CC=C1NC1=CC=CC=C1C WONYVCKUEUULQN-UHFFFAOYSA-N 0.000 description 1
JTMODJXOTWYBOZ-UHFFFAOYSA-N 2-methyl-n-phenylaniline Chemical compound CC1=CC=CC=C1NC1=CC=CC=C1 JTMODJXOTWYBOZ-UHFFFAOYSA-N 0.000 description 1
NZXZINXFUSKTPH-UHFFFAOYSA-N 4-[4-(4-butylcyclohexyl)cyclohexyl]-1,2-difluorobenzene Chemical compound C1CC(CCCC)CCC1C1CCC(C=2C=C(F)C(F)=CC=2)CC1 NZXZINXFUSKTPH-UHFFFAOYSA-N 0.000 description 1
WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
UUNBFTCKFYBASS-UHFFFAOYSA-N C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC Chemical compound C(CCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCC UUNBFTCKFYBASS-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
CUDSBWGCGSUXDB-UHFFFAOYSA-N Dibutyl disulfide Chemical compound CCCCSSCCCC CUDSBWGCGSUXDB-UHFFFAOYSA-N 0.000 description 1
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239000007787 solid Substances 0.000 description 1
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238000004448 titration Methods 0.000 description 1
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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
- C10M163/00—Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, each of these compounds being essential
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—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 type
- C10M2209/084—Acrylate; Methacrylate
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/066—Arylene diamines
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/067—Polyaryl amine alkanes
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/046—Overbased sulfonic acid salts
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
- 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
- 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
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
- 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
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02F—CYLINDERS, PISTONS OR CASINGS, FOR COMBUSTION ENGINES; ARRANGEMENTS OF SEALINGS IN COMBUSTION ENGINES
- F02F7/00—Casings, e.g. crankcases
- F02F7/006—Camshaft or pushrod housings

Landscapes

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

NL8201722A 1981-04-27 1982-04-26 Antioxydatiemiddelcombinaties van molybdeencomplexen en aromatische amineverbindingen. NL8201722A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/258,160 US4370246A (en)	1981-04-27	1981-04-27	Antioxidant combinations of molybdenum complexes and aromatic amine compounds
US25816081		1981-04-27

Publications (1)

Publication Number	Publication Date
NL8201722A true NL8201722A (nl)	1982-11-16

Family

ID=22979348

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8201722A NL8201722A (nl)	1981-04-27	1982-04-26	Antioxydatiemiddelcombinaties van molybdeencomplexen en aromatische amineverbindingen.

Country Status (14)

Country	Link
US (1)	US4370246A (fr)
JP (1)	JPS57185392A (fr)
AU (1)	AU545749B2 (fr)
BE (1)	BE892998A (fr)
BR (1)	BR8202408A (fr)
CA (1)	CA1176624A (fr)
DE (1)	DE3215656A1 (fr)
FR (1)	FR2504550B1 (fr)
GB (1)	GB2097422B (fr)
IT (1)	IT1151745B (fr)
MX (1)	MX7615E (fr)
NL (1)	NL8201722A (fr)
SE (1)	SE8202594L (fr)
ZA (1)	ZA822714B (fr)

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JP5175462B2 (ja)	2006-09-04	2013-04-03	出光興産株式会社	内燃機関用潤滑油組成物
JP5203590B2 (ja)	2006-10-27	2013-06-05	出光興産株式会社	潤滑油組成物
WO2008117776A1 (fr)	2007-03-28	2008-10-02	Idemitsu Kosan Co., Ltd.	Composition lubrifiante
JP5468728B2 (ja)	2007-05-29	2014-04-09	出光興産株式会社	内燃機関用潤滑油組成物
JP5379361B2 (ja)	2007-08-08	2013-12-25	出光興産株式会社	耐摩耗剤、潤滑剤用添加剤組成物及び潤滑油組成物
JP5198031B2 (ja) *	2007-10-22	2013-05-15	出光興産株式会社	潤滑油組成物
JP5571290B2 (ja)	2008-02-14	2014-08-13	出光興産株式会社	潤滑油組成物
US20090247434A1 (en) *	2008-03-31	2009-10-01	Chevron Oronite Company Llc	Preparation of a molybdenum amide additive composition and the lubricating oil compositions containing same
JP4597223B2 (ja)	2008-06-09	2010-12-15	出光興産株式会社	内燃機関用潤滑油組成物
JP5432493B2 (ja)	2008-10-09	2014-03-05	出光興産株式会社	内燃機関用潤滑油組成物
US20100152074A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
US20100152072A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
US20100152073A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
JPWO2011068137A1 (ja)	2009-12-03	2013-04-18	出光興産株式会社	潤滑油組成物
JP2011190331A (ja)	2010-03-12	2011-09-29	Idemitsu Kosan Co Ltd	潤滑油組成物
WO2011125880A1 (fr)	2010-04-02	2011-10-13	出光興産株式会社	Composition de lubrifiant pour un moteur à combustion interne
US9023190B2 (en)	2010-04-02	2015-05-05	Idemitsu Kosan Co., Ltd.	Lubricant composition for an internal combustion engine and method for lubricating an internal combustion engine
WO2011125879A1 (fr)	2010-04-02	2011-10-13	出光興産株式会社	Composition lubrifiante pour un moteur à combustion interne
US8334242B2 (en)	2010-10-12	2012-12-18	Chevron Oronite Company Llc	Lubricating composition containing multifunctional borated hydroxylated amine salt of a hindered phenolic acid
US8343901B2 (en)	2010-10-12	2013-01-01	Chevron Oronite Company Llc	Lubricating composition containing multifunctional hydroxylated amine salt of a hindered phenolic acid
WO2012071185A2 (fr)	2010-11-24	2012-05-31	Chevron Oronite Company Llc	Composition lubrifiante contenant mélange de modificateur de frottement
EP2883946B1 (fr)	2012-07-31	2019-06-12	Idemitsu Kosan Co., Ltd	Composition lubrifiante pour un moteur à combustion interne
EP2966153B1 (fr)	2013-03-08	2018-12-05	Idemitsu Kosan Co., Ltd	Utilisation d'une composition d'huile lubrifiante
CN105189720A (zh)	2013-03-08	2015-12-23	出光兴产株式会社	润滑油组合物
WO2014189057A1 (fr)	2013-05-20	2014-11-27	出光興産株式会社	Composition lubrifiante
KR20160090296A (ko)	2013-11-25	2016-07-29	이데미쓰 고산 가부시키가이샤	불꽃 점화식 내연 기관용 윤활유 조성물
JP6375117B2 (ja)	2014-01-27	2018-08-15	出光興産株式会社	内燃機関用潤滑油組成物
JP5952846B2 (ja)	2014-01-31	2016-07-13	出光興産株式会社	潤滑油組成物
US20190367833A1 (en) *	2016-12-27	2019-12-05	The Lubrizol Corporation	Lubricating composition including n-alkylated dianiline
WO2018125567A1 (fr)	2016-12-27	2018-07-05	The Lubrizol Corporation	Composition lubrifiante comportant une naphtylamine alkylée
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WO2020203524A1 (fr)	2019-03-29	2020-10-08	出光興産株式会社	Composition d'huile de graissage
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JPS5716095A (en) *	1980-06-13	1982-01-27	Texaco Development Corp	Production of lubricant additive

1981
- 1981-04-27 US US06/258,160 patent/US4370246A/en not_active Expired - Lifetime
1982
- 1982-04-07 CA CA000400654A patent/CA1176624A/fr not_active Expired
- 1982-04-13 AU AU82556/82A patent/AU545749B2/en not_active Ceased
- 1982-04-19 GB GB8211295A patent/GB2097422B/en not_active Expired
- 1982-04-19 FR FR8206686A patent/FR2504550B1/fr not_active Expired
- 1982-04-20 MX MX8210037U patent/MX7615E/es unknown
- 1982-04-21 ZA ZA822714A patent/ZA822714B/xx unknown
- 1982-04-26 SE SE8202594A patent/SE8202594L/ not_active Application Discontinuation
- 1982-04-26 NL NL8201722A patent/NL8201722A/nl not_active Application Discontinuation
- 1982-04-27 BE BE0/207947A patent/BE892998A/fr not_active IP Right Cessation
- 1982-04-27 JP JP57071129A patent/JPS57185392A/ja active Granted
- 1982-04-27 BR BR8202408A patent/BR8202408A/pt not_active IP Right Cessation
- 1982-04-27 DE DE19823215656 patent/DE3215656A1/de not_active Ceased
- 1982-04-27 IT IT20949/82A patent/IT1151745B/it active

Also Published As

Publication number	Publication date
JPS57185392A (en)	1982-11-15
BR8202408A (pt)	1983-04-12
FR2504550B1 (fr)	1986-08-29
IT8220949A0 (it)	1982-04-27
GB2097422A (en)	1982-11-03
ZA822714B (en)	1983-03-30
BE892998A (fr)	1982-08-16
CA1176624A (fr)	1984-10-23
SE8202594L (sv)	1982-10-28
FR2504550A1 (fr)	1982-10-29
IT1151745B (it)	1986-12-24
DE3215656A1 (de)	1982-11-18
GB2097422B (en)	1984-08-30
AU8255682A (en)	1982-11-04
MX7615E (es)	1990-03-27
US4370246A (en)	1983-01-25
JPH0322438B2 (fr)	1991-03-26
AU545749B2 (en)	1985-08-01

Legal Events

Date	Code	Title	Description
1985-01-01	A85	Still pending on 85-01-01
1987-12-01	BV	The patent application has lapsed

Publication	Publication Date	Title
US4370246A (en)	1983-01-25	Antioxidant combinations of molybdenum complexes and aromatic amine compounds
JP4956438B2 (ja)	2012-06-20	複数の酸化防止剤によって安定化された潤滑剤組成物
US4394279A (en)	1983-07-19	Antioxidant combinations of sulfur containing molybdenum complexes and aromatic amine compounds for lubricating oils
US8076275B2 (en)	2011-12-13	Reduced color molybdenum-containing composition and a method of making same
CA2189387C (fr)	2001-03-13	Lubrifiant renfermant un compose du molybdene et une diarylamine secondaire
US4259195A (en)	1981-03-31	Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same
NL8201414A (nl)	1982-11-01	Smeerolie toevoegsels, die combinaties van molybdenum complexen en organische zwavelverbindingen als antioxidatiemiddel bevatten.
USRE40595E1 (en)	2008-12-02	Lubricant containing molybdenum compound and secondary diarylamine
AU2013329028B2 (en)	2015-06-04	Lubricant compositions comprising boroxines to improve fluoropolymer seal compatibility
JPH07258671A (ja)	1995-10-09	無灰の低リン潤滑剤
US20080318815A1 (en)	2008-12-25	Synergistic lubricating oil composition containing a mixture of a nitro-substituted diarylamine and a dairylamine
AU2013302656A1 (en)	2015-03-05	Lubricant composition comprising acyclic hindered amines
US8623798B2 (en)	2014-01-07	Lubricating oil compositions containing a tetraalkyl-napthalene-1,8 diamine antioxidant
CA2909822A1 (fr)	2014-10-30	Additif de compatibilite avec les joints pour ameliorer la compatibilite avec les joints fluoropolymeres de compositions lubrifiantes
US3351647A (en)	1967-11-07	Nitrogen, phosphorus and metal containing composition
CN107922870B (zh)	2021-05-25	包含含硫和无硫有机钼化合物和三唑的润滑剂组合物添加剂
US4118329A (en)	1978-10-03	Amine phosphate salts and phosphoramides
CA1174032A (fr)	1984-09-11	Methode de preparation de complexes de molybdene, produits ainsi obtenus, et lubrifiants qui les renferment
US4118328A (en)	1978-10-03	Amine phosphate salts
EP3484983B1 (fr)	2020-05-27	Composition d'huile lubrifiante synergique contenant un mélange d'antioxydants
NL8003284A (nl)	1980-12-30	Molybdeenverbindingen, werkwijzen ter bereiding ervan alsmede smeeroliepreparaten, die deze verbindingen bevatten.