CA2836952C - Additive compositions with a friction modifier and a detergent - Google Patents
Additive compositions with a friction modifier and a detergent Download PDFInfo
- Publication number
- CA2836952C CA2836952C CA2836952A CA2836952A CA2836952C CA 2836952 C CA2836952 C CA 2836952C CA 2836952 A CA2836952 A CA 2836952A CA 2836952 A CA2836952 A CA 2836952A CA 2836952 C CA2836952 C CA 2836952C
- Authority
- CA
- Canada
- Prior art keywords
- engine oil
- engine
- oil
- formula
- detergent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 186
- 239000003599 detergent Substances 0.000 title claims abstract description 98
- 239000000654 additive Substances 0.000 title claims abstract description 95
- 239000003607 modifier Substances 0.000 title claims abstract description 91
- 230000000996 additive effect Effects 0.000 title claims abstract description 72
- 150000001875 compounds Chemical class 0.000 claims abstract description 111
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 108
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 77
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 53
- 239000002199 base oil Substances 0.000 claims abstract description 46
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 37
- 230000001050 lubricating effect Effects 0.000 claims abstract description 36
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 33
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 32
- 239000001257 hydrogen Substances 0.000 claims abstract description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 25
- 150000001340 alkali metals Chemical group 0.000 claims abstract description 24
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 21
- 150000001342 alkaline earth metals Chemical group 0.000 claims abstract description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 8
- 150000001768 cations Chemical class 0.000 claims abstract description 7
- -1 amine alcohols Chemical class 0.000 claims description 123
- 239000010705 motor oil Substances 0.000 claims description 87
- 239000003921 oil Substances 0.000 claims description 47
- 150000001412 amines Chemical class 0.000 claims description 46
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 34
- 229910052751 metal Inorganic materials 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 33
- 239000002184 metal Substances 0.000 claims description 32
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- 239000010409 thin film Substances 0.000 claims description 26
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 22
- 239000011575 calcium Substances 0.000 claims description 21
- 229910052791 calcium Inorganic materials 0.000 claims description 21
- 150000001298 alcohols Chemical class 0.000 claims description 20
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 19
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims description 19
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims description 19
- 239000003963 antioxidant agent Substances 0.000 claims description 19
- 239000002585 base Substances 0.000 claims description 19
- 229910052698 phosphorus Inorganic materials 0.000 claims description 19
- 239000011574 phosphorus Substances 0.000 claims description 19
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 18
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 15
- 239000011733 molybdenum Substances 0.000 claims description 15
- 229910052750 molybdenum Inorganic materials 0.000 claims description 15
- 239000011777 magnesium Substances 0.000 claims description 14
- 229910052749 magnesium Inorganic materials 0.000 claims description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 13
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 13
- 239000011734 sodium Substances 0.000 claims description 13
- 229910052708 sodium Inorganic materials 0.000 claims description 13
- 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 description 12
- 229910021529 ammonia Inorganic materials 0.000 claims description 11
- 150000001414 amino alcohols Chemical class 0.000 claims description 9
- 229910052744 lithium Inorganic materials 0.000 claims description 9
- 239000011591 potassium Substances 0.000 claims description 9
- 229910052700 potassium Inorganic materials 0.000 claims description 9
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 8
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 8
- 239000002518 antifoaming agent Substances 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 3
- ZMRQTIAUOLVKOX-UHFFFAOYSA-L calcium;diphenoxide Chemical compound [Ca+2].[O-]C1=CC=CC=C1.[O-]C1=CC=CC=C1 ZMRQTIAUOLVKOX-UHFFFAOYSA-L 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- AVVIDTZRJBSXML-UHFFFAOYSA-L calcium;2-carboxyphenolate;dihydrate Chemical compound O.O.[Ca+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O AVVIDTZRJBSXML-UHFFFAOYSA-L 0.000 claims description 2
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 claims description 2
- 229960004025 sodium salicylate Drugs 0.000 claims description 2
- 239000010687 lubricating oil Substances 0.000 description 71
- 239000012530 fluid Substances 0.000 description 48
- 235000019198 oils Nutrition 0.000 description 46
- 239000000314 lubricant Substances 0.000 description 39
- 239000002270 dispersing agent Substances 0.000 description 32
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 26
- 239000011541 reaction mixture Substances 0.000 description 24
- 150000002148 esters Chemical class 0.000 description 23
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- 229920002367 Polyisobutene Polymers 0.000 description 18
- 239000002253 acid Substances 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000005078 molybdenum compound Substances 0.000 description 17
- 125000001424 substituent group Chemical group 0.000 description 17
- BACYUWVYYTXETD-UHFFFAOYSA-N N-Lauroylsarcosine Chemical compound CCCCCCCCCCCC(=O)N(C)CC(O)=O BACYUWVYYTXETD-UHFFFAOYSA-N 0.000 description 16
- DIOYAVUHUXAUPX-KHPPLWFESA-N Oleoyl sarcosine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-KHPPLWFESA-N 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 16
- 239000003112 inhibitor Substances 0.000 description 16
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 15
- 150000002752 molybdenum compounds Chemical class 0.000 description 15
- 239000003513 alkali Substances 0.000 description 14
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 14
- 230000007935 neutral effect Effects 0.000 description 14
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- 229910052717 sulfur Inorganic materials 0.000 description 14
- 239000011593 sulfur Substances 0.000 description 14
- 150000001408 amides Chemical class 0.000 description 13
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 13
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 13
- 230000005540 biological transmission Effects 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- 150000001336 alkenes Chemical class 0.000 description 11
- 238000005461 lubrication Methods 0.000 description 11
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 11
- 229960001860 salicylate Drugs 0.000 description 11
- 230000002378 acidificating effect Effects 0.000 description 10
- 238000002485 combustion reaction Methods 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- 229930195733 hydrocarbon Natural products 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 10
- 150000002989 phenols Chemical class 0.000 description 10
- 230000003078 antioxidant effect Effects 0.000 description 9
- 239000004215 Carbon black (E152) Substances 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 8
- 229940071089 sarcosinate Drugs 0.000 description 8
- 108700004121 sarkosyl Proteins 0.000 description 8
- RJYOKYDKKOFLBT-UHFFFAOYSA-N 2-[methyl(octadecanoyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCCCCCC(=O)N(C)CC(O)=O RJYOKYDKKOFLBT-UHFFFAOYSA-N 0.000 description 7
- 125000002252 acyl group Chemical group 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 125000004494 ethyl ester group Chemical group 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 230000001603 reducing effect Effects 0.000 description 7
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 7
- YZUPZGFPHUVJKC-UHFFFAOYSA-N 1-bromo-2-methoxyethane Chemical compound COCCBr YZUPZGFPHUVJKC-UHFFFAOYSA-N 0.000 description 6
- DIOYAVUHUXAUPX-UHFFFAOYSA-N 2-[methyl(octadec-9-enoyl)amino]acetic acid Chemical compound CCCCCCCCC=CCCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-UHFFFAOYSA-N 0.000 description 6
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 229910052796 boron Inorganic materials 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 150000001735 carboxylic acids Chemical class 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 125000002811 oleoyl group Chemical group O=C([*])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 6
- 239000010734 process oil Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229960002317 succinimide Drugs 0.000 description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 108010077895 Sarcosine Proteins 0.000 description 5
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 5
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 5
- 239000000446 fuel Substances 0.000 description 5
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 5
- 229920013639 polyalphaolefin Polymers 0.000 description 5
- 150000003871 sulfonates Chemical class 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- ADOBXTDBFNCOBN-UHFFFAOYSA-N 1-heptadecene Chemical compound CCCCCCCCCCCCCCCC=C ADOBXTDBFNCOBN-UHFFFAOYSA-N 0.000 description 4
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- NGOZDSMNMIRDFP-UHFFFAOYSA-N 2-[methyl(tetradecanoyl)amino]acetic acid Chemical compound CCCCCCCCCCCCCC(=O)N(C)CC(O)=O NGOZDSMNMIRDFP-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- 150000001447 alkali salts Chemical class 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 230000000994 depressogenic effect Effects 0.000 description 4
- 150000005690 diesters Chemical class 0.000 description 4
- SYMLPHXUMNTFCM-UHFFFAOYSA-N ethyl 2-[dodecanoyl(methyl)amino]acetate Chemical compound CCCCCCCCCCCC(=O)N(C)CC(=O)OCC SYMLPHXUMNTFCM-UHFFFAOYSA-N 0.000 description 4
- WJAYSNLYCPKZJQ-UHFFFAOYSA-N ethyl 2-[methyl(octadec-9-enoyl)amino]acetate Chemical compound CCCCCCCCC=CCCCCCCCC(=O)N(C)CC(=O)OCC WJAYSNLYCPKZJQ-UHFFFAOYSA-N 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 239000003502 gasoline Substances 0.000 description 4
- VAMFXQBUQXONLZ-UHFFFAOYSA-N icos-1-ene Chemical compound CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- BMFVGAAISNGQNM-UHFFFAOYSA-N isopentylamine Chemical compound CC(C)CCN BMFVGAAISNGQNM-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 150000003873 salicylate salts Chemical class 0.000 description 4
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 3
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 3
- 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 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical class CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000010775 animal oil Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 3
- 229910001863 barium hydroxide Inorganic materials 0.000 description 3
- 159000000009 barium salts Chemical class 0.000 description 3
- 239000002551 biofuel Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 125000005266 diarylamine group Chemical group 0.000 description 3
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 3
- BTKSUULMJNNXHG-UHFFFAOYSA-N ethyl 2-(methylamino)acetate Chemical compound CCOC(=O)CNC BTKSUULMJNNXHG-UHFFFAOYSA-N 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical class C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 description 3
- 235000021313 oleic acid Nutrition 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 150000002924 oxiranes Chemical class 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920000193 polymethacrylate Polymers 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 3
- 239000013638 trimer Substances 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
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- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000001256 steam distillation Methods 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
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002277 temperature effect Effects 0.000 description 1
- 150000001911 terphenyls Chemical class 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229940095068 tetradecene Drugs 0.000 description 1
- JZALLXAUNPOCEU-UHFFFAOYSA-N tetradecylbenzene Chemical class CCCCCCCCCCCCCCC1=CC=CC=C1 JZALLXAUNPOCEU-UHFFFAOYSA-N 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000003396 thiol group Chemical class [H]S* 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000002469 tricosyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- VQOXUMQBYILCKR-UHFFFAOYSA-N tridecaene Natural products CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical class C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- ZBDJNBFTEIUHPK-UHFFFAOYSA-L zinc;dihexoxy-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].CCCCCCOP([S-])(=S)OCCCCCC.CCCCCCOP([S-])(=S)OCCCCCC ZBDJNBFTEIUHPK-UHFFFAOYSA-L 0.000 description 1
- USEBTXRETYRZKO-UHFFFAOYSA-L zinc;n,n-dioctylcarbamodithioate Chemical compound [Zn+2].CCCCCCCCN(C([S-])=S)CCCCCCCC.CCCCCCCCN(C([S-])=S)CCCCCCCC USEBTXRETYRZKO-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 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
- 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
- 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
- C10M133/16—Amides; Imides
-
- 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
-
- 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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/08—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium containing a sulfur-to-oxygen bond
- C10M135/10—Sulfonic acids or derivatives 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
- C10M139/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing atoms of elements not provided for in groups C10M127/00 - C10M137/00
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/028—Overbased 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
-
- 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
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated 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
- 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
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral 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
- C10M2219/04—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
- 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- 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
- C10N2010/08—Groups 4 or 14
-
- 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
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
-
- 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
- C10N2030/52—Base number [TBN]
-
- 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
- C10N2030/56—Boundary lubrication or thin film lubrication
-
- 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
- C10N2040/251—Alcohol-fuelled 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C10N2040/253—Small 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline 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
- C10N2040/255—Gasoline engines
- C10N2040/26—Two-strokes or two-cycle 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
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/725,411 | 2012-12-21 | ||
| US13/725,411 US9499762B2 (en) | 2012-12-21 | 2012-12-21 | Additive compositions with a friction modifier and a detergent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2836952A1 CA2836952A1 (en) | 2014-06-21 |
| CA2836952C true CA2836952C (en) | 2016-11-08 |
Family
ID=49911282
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2836952A Expired - Fee Related CA2836952C (en) | 2012-12-21 | 2013-12-13 | Additive compositions with a friction modifier and a detergent |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9499762B2 (enExample) |
| EP (1) | EP2746374B1 (enExample) |
| JP (1) | JP5956416B2 (enExample) |
| KR (1) | KR101683952B1 (enExample) |
| CN (1) | CN103881789A (enExample) |
| BR (1) | BR102013033043B1 (enExample) |
| CA (1) | CA2836952C (enExample) |
| SG (1) | SG2013094917A (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6698660B2 (ja) * | 2014-12-17 | 2020-05-27 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイＳｈｅｌｌ Ｉｎｔｅｒｎａｔｉｏｎａｌｅ Ｒｅｓｅａｒｃｈ Ｍａａｔｓｃｈａｐｐｉｊ Ｂｅｓｌｏｔｅｎ Ｖｅｎｎｏｏｔｓｈａｐ | 潤滑油組成物 |
| US10370611B2 (en) * | 2015-03-23 | 2019-08-06 | Lanxess Solutions Us Inc. | Low ash lubricant and fuel additive comprising alkoxylated amine |
| JP6551727B2 (ja) * | 2015-03-31 | 2019-07-31 | 出光興産株式会社 | 潤滑油組成物 |
| US11168280B2 (en) | 2015-10-05 | 2021-11-09 | Infineum International Limited | Additive concentrates for the formulation of lubricating oil compositions |
| WO2017159656A1 (ja) * | 2016-03-14 | 2017-09-21 | 味の素株式会社 | 化粧料組成物 |
| US10774064B2 (en) | 2016-06-02 | 2020-09-15 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| EP3263676B1 (en) * | 2016-06-30 | 2023-07-19 | Infineum International Limited | Lubricating oil compositions |
| US20180100114A1 (en) * | 2016-10-07 | 2018-04-12 | Exxonmobil Research And Engineering Company | Low conductivity lubricating oils for electric and hybrid vehicles |
| JP6714503B2 (ja) * | 2016-12-28 | 2020-06-24 | シェルルブリカンツジャパン株式会社 | 電子制御機器を配した油圧作動機用潤滑油組成物 |
| JP6997197B2 (ja) | 2017-01-23 | 2022-01-17 | カデント セラピューティクス，インコーポレーテッド | カリウムチャネルモジュレーター |
| JP6847684B2 (ja) * | 2017-02-01 | 2021-03-24 | Ｅｍｇルブリカンツ合同会社 | 潤滑油組成物 |
| RS63481B1 (sr) | 2017-11-30 | 2022-09-30 | Valvoline Licensing & Intellectual Property LLC | Modifikator trenja za motorno ulje |
| MX2021004647A (es) | 2018-10-22 | 2021-08-16 | Novartis Ag | Formas cristalinas de moduladores de los canales de potasio. |
| JP7304229B2 (ja) | 2019-07-18 | 2023-07-06 | 出光興産株式会社 | 潤滑油組成物 |
| JP7442287B2 (ja) * | 2019-09-26 | 2024-03-04 | Ｅｎｅｏｓ株式会社 | 内燃機関用潤滑油組成物 |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2061618A (en) | 1936-11-24 | Sulphonated hydrocarbon | ||
| US2841555A (en) | 1956-03-02 | 1958-07-01 | Texas Co | Metal nu-acyl sarcosinate thickened lubricating oils |
| US2905644A (en) | 1956-07-24 | 1959-09-22 | Commercial Solvents Corp | Anticorrosion agent |
| GB951139A (en) | 1960-10-24 | 1964-03-04 | Shell Int Research | Quenching oil composition |
| US3156653A (en) | 1961-09-29 | 1964-11-10 | California Research Corp | Transmission fluid |
| US3156652A (en) | 1961-09-29 | 1964-11-10 | California Research Corp | Automatic transmission fluid |
| BE672383A (enExample) | 1963-07-22 | |||
| FR1440207A (fr) | 1964-05-05 | 1966-05-27 | Sun Oil Co | Fluides anti-broutants pour transmission automatique |
| US3388068A (en) | 1964-05-05 | 1968-06-11 | Sun Oil Co | Nonsquawking automatic transmission fluids |
| US3332880A (en) | 1965-01-04 | 1967-07-25 | Procter & Gamble | Detergent composition |
| ZA672362B (enExample) | 1965-08-04 | |||
| US3506580A (en) | 1966-05-10 | 1970-04-14 | Colgate Palmolive Co | Heat-treatment of sulfonated olefin products |
| US3324155A (en) | 1966-08-02 | 1967-06-06 | John W Thompson | Amides of n-acyl sarcosines |
| US3420875A (en) | 1966-08-02 | 1969-01-07 | Colgate Palmolive Co | Olefin sulfonates |
| GB1235896A (en) | 1968-05-24 | 1971-06-16 | Mobil Oil Corp | Multifunctional fluid |
| US3640872A (en) * | 1968-10-25 | 1972-02-08 | Texaco Inc | Automatic transmission fluid |
| US3634515A (en) | 1968-11-08 | 1972-01-11 | Standard Oil Co | Alkylene polyamide formaldehyde |
| US3879306A (en) | 1973-11-05 | 1975-04-22 | Texaco Inc | Automatic transmission fluid |
| US3933659A (en) | 1974-07-11 | 1976-01-20 | Chevron Research Company | Extended life functional fluid |
| IT1054641B (it) | 1974-08-05 | 1981-11-30 | Mobil Oil Corp | Prodotti di reazione costituiti da aminoalcoli e composizioni che li contengono |
| US4035309A (en) | 1975-03-24 | 1977-07-12 | Exxon Research And Engineering Company | Metal-containing oxazoline additives and lubricating oils containing said additives |
| DD122102B1 (de) | 1975-10-15 | 1981-08-26 | Mineralölkomposition mit verbesserten Korrosionsschutzeigenschaften | |
| DE2702604C2 (de) | 1977-01-22 | 1984-08-30 | Basf Ag, 6700 Ludwigshafen | Polyisobutene |
| US4162224A (en) | 1977-01-28 | 1979-07-24 | Mobil Oil Corporation | Solubilized borates of bis-oxazoline and lubricant compositions containing the same |
| US4234435A (en) | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
| US4261843A (en) | 1979-06-28 | 1981-04-14 | Chevron Research Company | Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same |
| US4285822A (en) | 1979-06-28 | 1981-08-25 | Chevron Research Company | Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing the composition |
| US4259194A (en) | 1979-06-28 | 1981-03-31 | Chevron Research Company | Reaction product of ammonium tetrathiomolybdate with basic nitrogen compounds and lubricants containing same |
| US4265773A (en) | 1979-06-28 | 1981-05-05 | Chevron Research Company | Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same |
| US4283295A (en) | 1979-06-28 | 1981-08-11 | Chevron Research Company | Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing said composition |
| US4259195A (en) | 1979-06-28 | 1981-03-31 | Chevron Research Company | Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same |
| US4272387A (en) | 1979-06-28 | 1981-06-09 | Chevron Research Company | Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same |
| US4263152A (en) | 1979-06-28 | 1981-04-21 | Chevron Research Company | Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same |
| US4266944A (en) | 1979-12-17 | 1981-05-12 | Texaco Inc. | Fuel compositions containing acyl glycine oxazolines |
| US4374032A (en) | 1980-03-28 | 1983-02-15 | Mobil Oil Corporation | Lubricant composition containing borated oxazoline friction reducer |
| US4375418A (en) | 1981-10-28 | 1983-03-01 | Texaco Inc. | Lubricating oil composition |
| US4536307A (en) | 1983-09-23 | 1985-08-20 | Mobil Oil Corporation | Lubricant composition |
| US4645623A (en) | 1984-12-17 | 1987-02-24 | Monsanto Company | Alkylaryl sulfonate compositions |
| US4618436A (en) | 1985-07-01 | 1986-10-21 | Mobil Oil Corporation | Multifunctional lubricant additives and compositions thereof |
| JPS6227479A (ja) | 1985-07-29 | 1987-02-05 | Pentel Kk | ボ−ルペン用インキ組成物 |
| US5334329A (en) | 1988-10-07 | 1994-08-02 | The Lubrizol Corporation | Lubricant and functional fluid compositions exhibiting improved demulsibility |
| US5131921A (en) | 1990-10-09 | 1992-07-21 | Texaco Inc. | Polyoxyalkylene N-acyl sarcosinate ester compounds and ORI-inhibited motor fuel compositions |
| ES2101994T3 (es) | 1992-04-08 | 1997-07-16 | Ciba Geigy Ag | Antioxidantes liquidos como estabilizadores. |
| JPH0665589A (ja) | 1992-08-24 | 1994-03-08 | Showa Shell Sekiyu Kk | 水溶性切削油組成物 |
| WO1994006897A1 (en) | 1992-09-11 | 1994-03-31 | Chevron Research And Technology Company, A Division Of Chevron U.S.A. Inc. | Fuel composition for two-cycle engines |
| BR9400270A (pt) | 1993-02-18 | 1994-11-01 | Lubrizol Corp | Composição líquida e méthodo para lubrificar um compressor |
| SE500923C2 (sv) | 1993-10-21 | 1994-10-03 | Berol Nobel Ab | Användning av en amfotär tensid som friktionsreducerande medel i ett vattenbaserat vätskesystem |
| US5569407A (en) * | 1994-03-25 | 1996-10-29 | Mobil Oil Corporation | Additives for fuels and lubricants |
| US5538654A (en) | 1994-12-02 | 1996-07-23 | The Lubrizol Corporation | Environmental friendly food grade lubricants from edible triglycerides containing FDA approved additives |
| FR2730496B1 (fr) | 1995-02-15 | 1997-04-25 | Inst Francais Du Petrole | Procede de fabrication d'anhydride alkenyls ou polyalkenylsucciniques sans formation de resines |
| US6077455A (en) | 1995-07-17 | 2000-06-20 | Exxon Chemical Patents Inc | Automatic transmission fluid of improved viscometric properties |
| USRE38929E1 (en) | 1995-11-20 | 2006-01-03 | Afton Chemical Intangibles Llc | Lubricant containing molybdenum compound and secondary diarylamine |
| US5650381A (en) | 1995-11-20 | 1997-07-22 | Ethyl Corporation | Lubricant containing molybdenum compound and secondary diarylamine |
| ZA97222B (en) | 1996-01-16 | 1998-02-18 | Lubrizol Corp | Lubricating compositions. |
| US5599779A (en) | 1996-03-20 | 1997-02-04 | R. T. Vanderbilt Company, Inc. | Synergistic rust inhibitors and lubricating compositions |
| JPH09263782A (ja) | 1996-03-28 | 1997-10-07 | Idemitsu Kosan Co Ltd | 無段変速機油組成物 |
| DE60029049T2 (de) | 1999-05-19 | 2007-06-21 | Ciba Speciality Chemicals Holding Inc. | Stabilisierte hydroraffinierte und hydroentparaffinierte Schmiermittelzusammensetzungen |
| US6451745B1 (en) | 1999-05-19 | 2002-09-17 | The Lubrizol Corporation | High boron formulations for fluids continuously variable transmissions |
| US6300291B1 (en) | 1999-05-19 | 2001-10-09 | Infineum Usa L.P. | Lubricating oil composition |
| JP2002012884A (ja) | 2000-06-28 | 2002-01-15 | Nissan Motor Co Ltd | エンジン油組成物 |
| US7358217B2 (en) | 2001-12-18 | 2008-04-15 | The Lubrizol Corporation | Quenching oil compositions |
| US6723685B2 (en) | 2002-04-05 | 2004-04-20 | Infineum International Ltd. | Lubricating oil composition |
| NZ545920A (en) * | 2003-09-12 | 2009-10-30 | Renewable Lubricants Inc | Vegetable oil lubricant comprising all-hydroprocessed synthetic oils |
| US7214649B2 (en) | 2003-12-31 | 2007-05-08 | Afton Chemical Corporation | Hydrocarbyl dispersants including pendant polar functional groups |
| US7790660B2 (en) | 2004-02-13 | 2010-09-07 | Exxonmobil Research And Engineering Company | High efficiency polyalkylene glycol lubricants for use in worm gears |
| CN1938408A (zh) | 2004-03-25 | 2007-03-28 | 新日本石油株式会社 | 工业机械装置用润滑性组合物 |
| US20080058235A1 (en) | 2004-03-25 | 2008-03-06 | Katsuya Takigawa | Lubricative Composition for Industrial Machinery and Equipment |
| US7732390B2 (en) | 2004-11-24 | 2010-06-08 | Afton Chemical Corporation | Phenolic dimers, the process of preparing same and the use thereof |
| US7645726B2 (en) | 2004-12-10 | 2010-01-12 | Afton Chemical Corporation | Dispersant reaction product with antioxidant capability |
| JP2006265345A (ja) * | 2005-03-23 | 2006-10-05 | Sanyo Chem Ind Ltd | 船舶軸受け推進器用潤滑油 |
| JP4927349B2 (ja) * | 2005-05-11 | 2012-05-09 | 出光興産株式会社 | 冷凍機油組成物、これを用いた圧縮機及び冷凍装置 |
| CA2625029C (en) | 2005-10-11 | 2014-12-23 | The Lubrizol Corporation | Product of amines with hydroxy acid as friction modifiers suitable for automatic transmission fluids |
| US7691794B2 (en) | 2006-01-04 | 2010-04-06 | Chemtura Corporation | Lubricating oil and fuel compositions |
| JP5237562B2 (ja) | 2007-01-23 | 2013-07-17 | 昭和シェル石油株式会社 | セラミックス球転がり軸受用潤滑油組成物 |
| US7897696B2 (en) | 2007-02-01 | 2011-03-01 | Afton Chemical Corporation | Process for the preparation of polyalkenyl succinic anhydrides |
| EP2291498B1 (en) | 2008-05-13 | 2013-07-31 | The Lubrizol Corporation | Method to minimize turbo sludge with a polyether |
| EP2610330B1 (en) | 2008-09-16 | 2015-09-09 | The Lubrizol Corporation | Lubricant Composition |
| JP2012518046A (ja) * | 2009-02-13 | 2012-08-09 | ビーエーエスエフ ソシエタス・ヨーロピア | Ｎ−アシルサルコシン組成物 |
| US7977287B1 (en) | 2009-04-17 | 2011-07-12 | H2Oil Corporation | Microemulsion (nanotechnology) additive to oil |
| US8084403B2 (en) | 2009-05-01 | 2011-12-27 | Afton Chemical Corporation | Lubricant formulations and methods |
| JP5468297B2 (ja) | 2009-05-08 | 2014-04-09 | シェブロンジャパン株式会社 | 潤滑油組成物 |
| KR20130028033A (ko) | 2009-08-05 | 2013-03-18 | 바스프 에스이 | 윤활 조성물 |
| WO2011017637A1 (en) * | 2009-08-07 | 2011-02-10 | Basf Se | Lubricant composition comprising alkylethercarboxylic acid |
| WO2011030615A1 (ja) * | 2009-09-09 | 2011-03-17 | Ｊｘ日鉱日石エネルギー株式会社 | さび止め油組成物 |
| US9725673B2 (en) | 2010-03-25 | 2017-08-08 | Afton Chemical Corporation | Lubricant compositions for improved engine performance |
| EP2625254B1 (en) | 2010-10-06 | 2021-02-24 | The Lubrizol Corporation | Use of a lubricating oil composition in a direct injection gasoline engine |
| US8999905B2 (en) | 2010-10-25 | 2015-04-07 | Afton Chemical Corporation | Lubricant additive |
| JP5504137B2 (ja) | 2010-11-12 | 2014-05-28 | Ｊｘ日鉱日石エネルギー株式会社 | エンジン油組成物 |
| CN102329681A (zh) * | 2011-09-05 | 2012-01-25 | 王琴 | 齿轮润滑添加剂 |
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2012
- 2012-12-21 US US13/725,411 patent/US9499762B2/en active Active
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2013
- 2013-12-13 CA CA2836952A patent/CA2836952C/en not_active Expired - Fee Related
- 2013-12-17 JP JP2013260208A patent/JP5956416B2/ja active Active
- 2013-12-20 KR KR1020130160643A patent/KR101683952B1/ko active Active
- 2013-12-20 BR BR102013033043A patent/BR102013033043B1/pt not_active IP Right Cessation
- 2013-12-20 EP EP13199016.0A patent/EP2746374B1/en active Active
- 2013-12-20 SG SG2013094917A patent/SG2013094917A/en unknown
- 2013-12-23 CN CN201310714844.8A patent/CN103881789A/zh active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP2746374A3 (en) | 2014-09-10 |
| JP5956416B2 (ja) | 2016-07-27 |
| KR20140081746A (ko) | 2014-07-01 |
| SG2013094917A (en) | 2014-07-30 |
| CN103881789A (zh) | 2014-06-25 |
| JP2014122343A (ja) | 2014-07-03 |
| BR102013033043B1 (pt) | 2017-05-30 |
| BR102013033043A2 (pt) | 2015-09-08 |
| US9499762B2 (en) | 2016-11-22 |
| US20140179577A1 (en) | 2014-06-26 |
| CA2836952A1 (en) | 2014-06-21 |
| EP2746374A2 (en) | 2014-06-25 |
| EP2746374B1 (en) | 2018-08-29 |
| KR101683952B1 (ko) | 2016-12-07 |
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