ZA200205676B - Formulated lubricant oils containing high-performance base oils derived from highly paraffinic hydrocarbons. - Google Patents
Formulated lubricant oils containing high-performance base oils derived from highly paraffinic hydrocarbons. Download PDFInfo
- Publication number
- ZA200205676B ZA200205676B ZA200205676A ZA200205676A ZA200205676B ZA 200205676 B ZA200205676 B ZA 200205676B ZA 200205676 A ZA200205676 A ZA 200205676A ZA 200205676 A ZA200205676 A ZA 200205676A ZA 200205676 B ZA200205676 B ZA 200205676B
- Authority
- ZA
- South Africa
- Prior art keywords
- viscosity
- lubricant composition
- liquid lubricant
- cst
- basestock
- Prior art date
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- 239000000314 lubricant Substances 0.000 title claims description 90
- 150000002430 hydrocarbons Chemical class 0.000 title claims description 70
- 229930195733 hydrocarbon Natural products 0.000 title claims description 67
- 239000003921 oil Substances 0.000 title description 70
- 239000002199 base oil Substances 0.000 title description 49
- 239000000203 mixture Substances 0.000 claims description 125
- 239000004215 Carbon black (E152) Substances 0.000 claims description 57
- 239000010687 lubricating oil Substances 0.000 claims description 50
- 239000000654 additive Substances 0.000 claims description 36
- 150000002148 esters Chemical class 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- -1 alkyl naphthalene Chemical compound 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 239000003963 antioxidant agent Substances 0.000 claims description 10
- 239000003599 detergent Substances 0.000 claims description 9
- 150000004982 aromatic amines Chemical class 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims 3
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 claims 1
- 229960001860 salicylate Drugs 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- 239000001993 wax Substances 0.000 description 103
- 238000009472 formulation Methods 0.000 description 39
- 229920013639 polyalphaolefin Polymers 0.000 description 36
- 238000012360 testing method Methods 0.000 description 31
- 239000012530 fluid Substances 0.000 description 29
- 239000010705 motor oil Substances 0.000 description 25
- 239000000463 material Substances 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 23
- 238000000034 method Methods 0.000 description 21
- 229920000642 polymer Polymers 0.000 description 18
- 230000000996 additive effect Effects 0.000 description 14
- 238000006065 biodegradation reaction Methods 0.000 description 14
- 239000003054 catalyst Substances 0.000 description 14
- 239000002270 dispersing agent Substances 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 238000010998 test method Methods 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- 239000003607 modifier Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- 229910021536 Zeolite Inorganic materials 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 6
- 150000004996 alkyl benzenes Chemical class 0.000 description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000010457 zeolite Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 5
- 239000002530 phenolic antioxidant Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical class CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 3
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000005069 Extreme pressure additive Substances 0.000 description 3
- 101150092791 PAO4 gene Proteins 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000008186 active pharmaceutical agent Substances 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000002518 distortionless enhancement with polarization transfer Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 238000006317 isomerization reaction Methods 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 235000013824 polyphenols Nutrition 0.000 description 3
- 238000012797 qualification Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- IHQZONJYGAQKGK-UHFFFAOYSA-N 2-tert-butyl-4-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C(C(C)(C)C)=C1 IHQZONJYGAQKGK-UHFFFAOYSA-N 0.000 description 2
- XCIGNJPXXAPZDP-UHFFFAOYSA-N 2-tert-butyl-4-heptylphenol Chemical compound CCCCCCCC1=CC=C(O)C(C(C)(C)C)=C1 XCIGNJPXXAPZDP-UHFFFAOYSA-N 0.000 description 2
- ZXENURKTAAQNOU-UHFFFAOYSA-N 2-tert-butyl-4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C(C(C)(C)C)=C1 ZXENURKTAAQNOU-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000003042 antagnostic effect Effects 0.000 description 2
- SCJNCDSAIRBRIA-DOFZRALJSA-N arachidonyl-2'-chloroethylamide Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCCl SCJNCDSAIRBRIA-DOFZRALJSA-N 0.000 description 2
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical class [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 229920000359 diblock copolymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229940069096 dodecene Drugs 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910001657 ferrierite group Inorganic materials 0.000 description 2
- 239000012208 gear oil Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000003879 lubricant additive Substances 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
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- 238000002156 mixing Methods 0.000 description 2
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- 150000002790 naphthalenes Chemical class 0.000 description 2
- 125000005609 naphthenate group Chemical group 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 150000003902 salicylic acid esters Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
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- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- CIRMGZKUSBCWRL-LHLOQNFPSA-N (e)-10-[2-(7-carboxyheptyl)-5,6-dihexylcyclohex-3-en-1-yl]dec-9-enoic acid Chemical compound CCCCCCC1C=CC(CCCCCCCC(O)=O)C(\C=C\CCCCCCCC(O)=O)C1CCCCCC CIRMGZKUSBCWRL-LHLOQNFPSA-N 0.000 description 1
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 description 1
- RLPSARLYTKXVSE-UHFFFAOYSA-N 1-(1,3-thiazol-5-yl)ethanamine Chemical compound CC(N)C1=CN=CS1 RLPSARLYTKXVSE-UHFFFAOYSA-N 0.000 description 1
- GLEAJEPGOSMZLQ-UHFFFAOYSA-N 1-octyl-n-(4-octylphenyl)naphthalen-2-amine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(C=CC=C2)C2=C1CCCCCCCC GLEAJEPGOSMZLQ-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical class CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- SZATXRHXOOLEFV-UHFFFAOYSA-N 2,6-ditert-butyl-4-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SZATXRHXOOLEFV-UHFFFAOYSA-N 0.000 description 1
- OEHMRECZRLQSRD-UHFFFAOYSA-N 2,6-ditert-butyl-4-heptylphenol Chemical compound CCCCCCCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 OEHMRECZRLQSRD-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical class ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- SZSSMFVYZRQGIM-UHFFFAOYSA-N 2-(hydroxymethyl)-2-propylpropane-1,3-diol Chemical compound CCCC(CO)(CO)CO SZSSMFVYZRQGIM-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- JVZZUPJFERSVRN-UHFFFAOYSA-N 2-methyl-2-propylpropane-1,3-diol Chemical compound CCCC(C)(CO)CO JVZZUPJFERSVRN-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- NUCFNMOPTGEHQA-UHFFFAOYSA-N 3-bromo-2h-pyrazolo[4,3-c]pyridine Chemical compound C1=NC=C2C(Br)=NNC2=C1 NUCFNMOPTGEHQA-UHFFFAOYSA-N 0.000 description 1
- CLPFFLWZZBQMAO-UHFFFAOYSA-N 4-(5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-5-yl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1C1N2C=NC=C2CCC1 CLPFFLWZZBQMAO-UHFFFAOYSA-N 0.000 description 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 206010016807 Fluid retention Diseases 0.000 description 1
- 239000004169 Hydrogenated Poly-1-Decene Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- 238000012565 NMR experiment Methods 0.000 description 1
- 231100000694 OECD Guidelines for the Testing of Chemicals Toxicity 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- QAPVYZRWKDXNDK-UHFFFAOYSA-N P,P-Dioctyldiphenylamine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=C(CCCCCCCC)C=C1 QAPVYZRWKDXNDK-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000035508 accumulation Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
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- 238000013019 agitation Methods 0.000 description 1
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- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- WLLCYXDFVBWGBU-UHFFFAOYSA-N bis(8-methylnonyl) nonanedioate Chemical compound CC(C)CCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC(C)C WLLCYXDFVBWGBU-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- VLLYOYVKQDKAHN-UHFFFAOYSA-N buta-1,3-diene;2-methylbuta-1,3-diene Chemical compound C=CC=C.CC(=C)C=C VLLYOYVKQDKAHN-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229940000425 combination drug Drugs 0.000 description 1
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- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 229940100539 dibutyl adipate Drugs 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
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- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
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- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
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- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
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- 229960002523 mercuric chloride Drugs 0.000 description 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
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- 239000006078 metal deactivator Substances 0.000 description 1
- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 description 1
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- 238000012986 modification Methods 0.000 description 1
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- 150000002751 molybdenum Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000010707 multi-grade lubricating oil Substances 0.000 description 1
- BQLZCNHPJNMDIO-UHFFFAOYSA-N n-(4-octylphenyl)naphthalen-1-amine Chemical compound C1=CC(CCCCCCCC)=CC=C1NC1=CC=CC2=CC=CC=C12 BQLZCNHPJNMDIO-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- SNWVRVDHQRBBFG-UHFFFAOYSA-N n-phenyl-n-(2,4,4-trimethylpentan-2-yl)naphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(C(C)(C)CC(C)(C)C)C1=CC=CC=C1 SNWVRVDHQRBBFG-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002990 phenothiazines Chemical class 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical group 0.000 description 1
- 125000005017 substituted alkenyl group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 229920000428 triblock copolymer Polymers 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- FDQVRICZJAZAMX-UHFFFAOYSA-L zinc;4-methylpentoxy-(4-methylpentylsulfanyl)-oxido-sulfanylidene-$l^{5}-phosphane Chemical compound [Zn+2].CC(C)CCCOP([O-])(=S)SCCCC(C)C.CC(C)CCCOP([O-])(=S)SCCCC(C)C FDQVRICZJAZAMX-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/02—Specified values of viscosity or viscosity index
-
- 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/048—Mixtures of base-materials and additives the additives being a mixture of compounds of unknown or incompletely defined constitution, non-macromolecular and macromolecular compounds
-
- 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
- C10M177/00—Special methods of preparation of lubricating compositions; Chemical modification by after-treatment of components or of the whole of a lubricating composition, not covered by other classes
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
- C10M2203/065—Well-defined aromatic compounds used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/06—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
-
- 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
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl 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
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
- C10M2207/2835—Esters of polyhydroxy compounds used as base material
-
- 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
-
- 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—Overbasedsulfonic acid salts
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/071—Branched chain compounds
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/081—Biodegradable compounds
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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/498,793 US7067049B1 (en) | 2000-02-04 | 2000-02-04 | Formulated lubricant oils containing high-performance base oils derived from highly paraffinic hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200205676B true ZA200205676B (en) | 2003-11-13 |
Family
ID=23982522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200205676A ZA200205676B (en) | 2000-02-04 | 2002-07-16 | Formulated lubricant oils containing high-performance base oils derived from highly paraffinic hydrocarbons. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7067049B1 (fr) |
| EP (1) | EP1252279A1 (fr) |
| JP (1) | JP2003528169A (fr) |
| KR (1) | KR20020074226A (fr) |
| CN (1) | CN1398292A (fr) |
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Families Citing this family (200)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2002249198B2 (en) * | 2001-02-13 | 2006-10-12 | Shell Internationale Research Maatschappij B.V. | Lubricant composition |
| AR032930A1 (es) | 2001-03-05 | 2003-12-03 | Shell Int Research | Procedimiento para preparar un aceite de base lubricante y gas oil |
| MY137259A (en) | 2001-03-05 | 2009-01-30 | Shell Int Research | Process to prepare a lubricating base oil and a gas oil. |
| AR032941A1 (es) | 2001-03-05 | 2003-12-03 | Shell Int Research | Un procedimiento para preparar un aceite base lubricante y aceite base obtenido, con sus diversas utilizaciones |
| WO2004003113A1 (fr) * | 2002-06-26 | 2004-01-08 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| ES2254973T3 (es) | 2002-07-18 | 2006-06-16 | Shell Internationale Research Maatschappij B.V. | Procedimiento de preparacion de una cera microcristalina y de un combustible de destilado medio. |
| US6703353B1 (en) * | 2002-09-04 | 2004-03-09 | Chevron U.S.A. Inc. | Blending of low viscosity Fischer-Tropsch base oils to produce high quality lubricating base oils |
| US20040129603A1 (en) * | 2002-10-08 | 2004-07-08 | Fyfe Kim Elizabeth | High viscosity-index base stocks, base oils and lubricant compositions and methods for their production and use |
| US7704379B2 (en) * | 2002-10-08 | 2010-04-27 | Exxonmobil Research And Engineering Company | Dual catalyst system for hydroisomerization of Fischer-Tropsch wax and waxy raffinate |
| US7344631B2 (en) | 2002-10-08 | 2008-03-18 | Exxonmobil Research And Engineering Company | Oxygenate treatment of dewaxing catalyst for greater yield of dewaxed product |
| US7144497B2 (en) | 2002-11-20 | 2006-12-05 | Chevron U.S.A. Inc. | Blending of low viscosity Fischer-Tropsch base oils with conventional base oils to produce high quality lubricating base oils |
| US20040119046A1 (en) * | 2002-12-11 | 2004-06-24 | Carey James Thomas | Low-volatility functional fluid compositions useful under conditions of high thermal stress and methods for their production and use |
| US20040154958A1 (en) * | 2002-12-11 | 2004-08-12 | Alexander Albert Gordon | Functional fluids having low brookfield viscosity using high viscosity-index base stocks, base oils and lubricant compositions, and methods for their production and use |
| US20040154957A1 (en) * | 2002-12-11 | 2004-08-12 | Keeney Angela J. | High viscosity index wide-temperature functional fluid compositions and methods for their making and use |
| SG117798A1 (en) | 2003-06-23 | 2008-02-29 | Shell Int Research | Process to prepare a lubricating base oil |
| US20070272592A1 (en) | 2003-06-27 | 2007-11-29 | Germaine Gilbert R B | Process to Prepare a Lubricating Base Oil |
| US20050077208A1 (en) * | 2003-10-14 | 2005-04-14 | Miller Stephen J. | Lubricant base oils with optimized branching |
| US7053254B2 (en) * | 2003-11-07 | 2006-05-30 | Chevron U.S.A, Inc. | Process for improving the lubricating properties of base oils using a Fischer-Tropsch derived bottoms |
| US7195706B2 (en) | 2003-12-23 | 2007-03-27 | Chevron U.S.A. Inc. | Finished lubricating comprising lubricating base oil with high monocycloparaffins and low multicycloparaffins |
| US7763161B2 (en) | 2003-12-23 | 2010-07-27 | Chevron U.S.A. Inc. | Process for making lubricating base oils with high ratio of monocycloparaffins to multicycloparaffins |
| EP1548088A1 (fr) | 2003-12-23 | 2005-06-29 | Shell Internationale Researchmaatschappij B.V. | Procédé de préparation d'une huile de base non-trouble |
| US7282134B2 (en) | 2003-12-23 | 2007-10-16 | Chevron Usa, Inc. | Process for manufacturing lubricating base oil with high monocycloparaffins and low multicycloparaffins |
| US7083713B2 (en) | 2003-12-23 | 2006-08-01 | Chevron U.S.A. Inc. | Composition of lubricating base oil with high monocycloparaffins and low multicycloparaffins |
| CA2570514A1 (fr) | 2004-06-18 | 2005-12-29 | Shell Internationale Research Maatschappij B.V. | Composition d'huile lubrifiantes |
| US7550415B2 (en) | 2004-12-10 | 2009-06-23 | Shell Oil Company | Lubricating oil composition |
| US20070293408A1 (en) * | 2005-03-11 | 2007-12-20 | Chevron Corporation | Hydraulic Fluid Compositions and Preparation Thereof |
| US7674364B2 (en) * | 2005-03-11 | 2010-03-09 | Chevron U.S.A. Inc. | Hydraulic fluid compositions and preparation thereof |
| US20080053868A1 (en) * | 2005-06-22 | 2008-03-06 | Chevron U.S.A. Inc. | Engine oil compositions and preparation thereof |
| BRPI0611907B1 (pt) | 2005-06-23 | 2015-09-22 | Shell Int Research | Formulação de óleo elétrico, processo para preparar a mesma, e, uso da formulação |
| EP1893728A1 (fr) * | 2005-06-23 | 2008-03-05 | Shell Internationale Research Maatschappij B.V. | Composition d'huile lubrifiante |
| JP2009511728A (ja) | 2005-10-17 | 2009-03-19 | 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 | 潤滑油組成物 |
| US7732386B2 (en) * | 2005-10-25 | 2010-06-08 | Chevron U.S.A. Inc. | Rust inhibitor for highly paraffinic lubricating base oil |
| CA2643358A1 (fr) | 2006-02-21 | 2007-08-30 | Shell Internationale Research Maatschappij B.V. | Composition d'huile lubrifiante |
| CN101405376B (zh) * | 2006-03-22 | 2012-10-17 | 国际壳牌研究有限公司 | 功能性流体组合物 |
| JP5498644B2 (ja) * | 2006-07-06 | 2014-05-21 | Ｊｘ日鉱日石エネルギー株式会社 | 駆動伝達装置用潤滑油組成物 |
| JP4945178B2 (ja) * | 2006-07-06 | 2012-06-06 | Ｊｘ日鉱日石エネルギー株式会社 | 内燃機関用潤滑油組成物 |
| JP4945179B2 (ja) * | 2006-07-06 | 2012-06-06 | Ｊｘ日鉱日石エネルギー株式会社 | 内燃機関用潤滑油組成物 |
| JP2007270062A (ja) * | 2006-03-31 | 2007-10-18 | Nippon Oil Corp | 潤滑油基油、潤滑油組成物及び潤滑油基油の製造方法 |
| JP4945180B2 (ja) * | 2006-07-06 | 2012-06-06 | Ｊｘ日鉱日石エネルギー株式会社 | 湿式クラッチ用潤滑油組成物 |
| JP5137314B2 (ja) * | 2006-03-31 | 2013-02-06 | Ｊｘ日鉱日石エネルギー株式会社 | 潤滑油基油 |
| US7863229B2 (en) | 2006-06-23 | 2011-01-04 | Exxonmobil Research And Engineering Company | Lubricating compositions |
| US20080110797A1 (en) * | 2006-10-27 | 2008-05-15 | Fyfe Kim E | Formulated lubricants meeting 0W and 5W low temperature performance specifications made from a mixture of base stocks obtained by different final wax processing routes |
| US20100004148A1 (en) * | 2006-11-10 | 2010-01-07 | David Colbourne | Low sulfur, low sulfated ash, low phosphorus and highly paraffinic lubricant composition |
| US20080128322A1 (en) * | 2006-11-30 | 2008-06-05 | Chevron Oronite Company Llc | Traction coefficient reducing lubricating oil composition |
| US8258087B2 (en) | 2006-12-08 | 2012-09-04 | Nippon Oil Corporation | Lubricating oil composition for internal combustion engine |
| JP5325384B2 (ja) * | 2006-12-08 | 2013-10-23 | Ｊｘ日鉱日石エネルギー株式会社 | 内燃機関用潤滑油組成物 |
| JP5108315B2 (ja) | 2007-02-01 | 2012-12-26 | 昭和シェル石油株式会社 | 有機モリブデン化合物よりなる摩擦調整剤およびそれを含む潤滑組成物 |
| JP5108318B2 (ja) | 2007-02-01 | 2012-12-26 | 昭和シェル石油株式会社 | 新規な有機モリブデン化合物 |
| JP5108317B2 (ja) | 2007-02-01 | 2012-12-26 | 昭和シェル石油株式会社 | アルキルキサントゲン酸モリブデン、それよりなる摩擦調整剤およびそれを含む潤滑組成物 |
| US7307049B1 (en) * | 2007-02-08 | 2007-12-11 | Anderol, Inc. | Antioxidants for synthetic lubricants and methods and manufacture |
| US20080300157A1 (en) * | 2007-03-30 | 2008-12-04 | Wu Margaret M | Lubricating oil compositions having improved low temperature properties |
| US20090036546A1 (en) * | 2007-07-31 | 2009-02-05 | Chevron U.S.A. Inc. | Medicinal Oil Compositions, Preparations, and Applications Thereof |
| US20090036333A1 (en) * | 2007-07-31 | 2009-02-05 | Chevron U.S.A. Inc. | Metalworking Fluid Compositions and Preparation Thereof |
| US20090036337A1 (en) * | 2007-07-31 | 2009-02-05 | Chevron U.S.A. Inc. | Electrical Insulating Oil Compositions and Preparation Thereof |
| US20090036338A1 (en) * | 2007-07-31 | 2009-02-05 | Chevron U.S.A. Inc. | Metalworking Fluid Compositions and Preparation Thereof |
| US20090062162A1 (en) * | 2007-08-28 | 2009-03-05 | Chevron U.S.A. Inc. | Gear oil composition, methods of making and using thereof |
| US20090062163A1 (en) * | 2007-08-28 | 2009-03-05 | Chevron U.S.A. Inc. | Gear Oil Compositions, Methods of Making and Using Thereof |
| US7932217B2 (en) * | 2007-08-28 | 2011-04-26 | Chevron U.S.A., Inc. | Gear oil compositions, methods of making and using thereof |
| US20090088352A1 (en) * | 2007-09-27 | 2009-04-02 | Chevron U.S.A. Inc. | Tractor hydraulic fluid compositions and preparation thereof |
| US20090088353A1 (en) * | 2007-09-27 | 2009-04-02 | Chevron U.S.A. Inc. | Lubricating grease composition and preparation |
| CA2702860A1 (fr) | 2007-10-19 | 2009-04-23 | Mark Lawrence Brewer | Fluides fonctionnels pour moteurs a combustion interne |
| EP2071008A1 (fr) | 2007-12-04 | 2009-06-17 | Shell Internationale Researchmaatschappij B.V. | Composition de lubrification contenant imidazolidinethione et imidazolidone |
| US7956018B2 (en) * | 2007-12-10 | 2011-06-07 | Chevron U.S.A. Inc. | Lubricant composition |
| EP2075314A1 (fr) * | 2007-12-11 | 2009-07-01 | Shell Internationale Research Maatschappij B.V. | Formules de graisse |
| EP2072610A1 (fr) * | 2007-12-11 | 2009-06-24 | Shell Internationale Research Maatschappij B.V. | Composition d'huile support |
| US20090181871A1 (en) * | 2007-12-19 | 2009-07-16 | Chevron U.S.A. Inc. | Compressor Lubricant Compositions and Preparation Thereof |
| US20090163391A1 (en) * | 2007-12-20 | 2009-06-25 | Chevron U.S.A. Inc. | Power Transmission Fluid Compositions and Preparation Thereof |
| AR070686A1 (es) | 2008-01-16 | 2010-04-28 | Shell Int Research | Un metodo para preparar una composicion de lubricante |
| US20090298732A1 (en) * | 2008-05-29 | 2009-12-03 | Chevron U.S.A. Inc. | Gear oil compositions, methods of making and using thereof |
| EP2300578B1 (fr) | 2008-06-19 | 2016-07-20 | Shell Internationale Research Maatschappij B.V. | Compositions de graisse lubrifiante |
| CN102105572A (zh) | 2008-06-24 | 2011-06-22 | 国际壳牌研究有限公司 | 包含聚(羟基羧酸)酰胺的润滑组合物的用途 |
| CN102124086A (zh) | 2008-07-31 | 2011-07-13 | 国际壳牌研究有限公司 | 聚(羟基羧酸)酰胺盐衍生物和包含它的润滑组合物 |
| US20100162693A1 (en) | 2008-12-31 | 2010-07-01 | Michael Paul W | Method of reducing torque ripple in hydraulic motors |
| WO2010086365A1 (fr) | 2009-01-28 | 2010-08-05 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| EP2186871A1 (fr) | 2009-02-11 | 2010-05-19 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| WO2010094681A1 (fr) | 2009-02-18 | 2010-08-26 | Shell Internationale Research Maatschappij B.V. | Utilisation d'une composition lubrifiante avec de l'huile à base de gtl pour réduire les émissions d'hydrocarbure |
| EP2248878A1 (fr) | 2009-05-01 | 2010-11-10 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| BRPI1012250B1 (pt) | 2009-06-24 | 2018-05-15 | Shell Internationale Research Maatschappij B.V. | Composição lubrificante, e, uso de uma composição lubrificante |
| WO2010149712A1 (fr) | 2009-06-25 | 2010-12-29 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| US8822394B2 (en) | 2009-08-18 | 2014-09-02 | Shell Oil Company | Lubricating grease compositions |
| EP2470626A1 (fr) | 2009-08-28 | 2012-07-04 | Shell Internationale Research Maatschappij B.V. | Composition d huile de traitement |
| EP2486113B2 (fr) | 2009-10-09 | 2022-12-07 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| EP2159275A3 (fr) | 2009-10-14 | 2010-04-28 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| US8663454B2 (en) * | 2009-10-23 | 2014-03-04 | Chevron U.S.A. Inc. | Formulating a sealant fluid using gas to liquid base stocks |
| EP2494014B1 (fr) | 2009-10-26 | 2015-12-16 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| EP2189515A1 (fr) | 2009-11-05 | 2010-05-26 | Shell Internationale Research Maatschappij B.V. | Composition liquide fonctionnelle |
| EP2186872A1 (fr) | 2009-12-16 | 2010-05-19 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| JP2013515802A (ja) | 2009-12-24 | 2013-05-09 | 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 | 液体燃料組成物 |
| RU2012132488A (ru) | 2009-12-29 | 2014-02-10 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Композиции жидких топлив |
| WO2011110551A1 (fr) | 2010-03-10 | 2011-09-15 | Shell Internationale Research Maatschappij B.V. | Procédé de réduction de la toxicité de compositions lubrifiantes usagées |
| EP2547753A1 (fr) | 2010-03-17 | 2013-01-23 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| EP2194114A3 (fr) | 2010-03-19 | 2010-10-27 | Shell Internationale Research Maatschappij B.V. | Schmiermittelzusammensetzung |
| EP2385097A1 (fr) | 2010-05-03 | 2011-11-09 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| EP2566940B1 (fr) | 2010-05-03 | 2019-01-09 | Shell International Research Maatschappij B.V. | Utilisation d'huile de base fischer-tropsch pour réduire la toxicité de compositions lubrifiantes usées |
| US8318643B2 (en) * | 2010-06-29 | 2012-11-27 | Cherron Oronite Technology B.V. | Trunk piston engine lubricating oil compositions |
| EP2591080B1 (fr) | 2010-07-05 | 2014-11-26 | Shell Internationale Research Maatschappij B.V. | Procédé pour la fabrication d'une composition de graisse |
| WO2012017023A1 (fr) | 2010-08-03 | 2012-02-09 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| EP2441818A1 (fr) | 2010-10-12 | 2012-04-18 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| US8784642B2 (en) | 2010-11-29 | 2014-07-22 | Chevron Japan Ltd. | Lubricating oil composition for lubricating automotive engines |
| EP2457985B1 (fr) * | 2010-11-29 | 2020-04-22 | Chevron Japan Ltd. | Composition d'huile lubrifiante pour lubrifier des moteurs d'automobile |
| JP5898691B2 (ja) | 2010-12-17 | 2016-04-06 | 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 Ｂｅｓｌｏｔｅｎｖｅｎｎｏｏｔｓｈａｐ | 潤滑組成物 |
| WO2012150283A1 (fr) | 2011-05-05 | 2012-11-08 | Shell Internationale Research Maatschappij B.V. | Compositions d'huile de lubrification comprenant des huiles de base dérivées de fischer-tropsch |
| US20120304531A1 (en) | 2011-05-30 | 2012-12-06 | Shell Oil Company | Liquid fuel compositions |
| EP2395068A1 (fr) | 2011-06-14 | 2011-12-14 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| US9593267B2 (en) | 2011-12-20 | 2017-03-14 | Shell Oil Company | Adhesive compositions and methods of using the same |
| WO2013093103A1 (fr) | 2011-12-22 | 2013-06-27 | Shell Internationale Research Maatschappij B.V. | Composition de graissage |
| US20140357825A1 (en) | 2011-12-22 | 2014-12-04 | Shell Internationale Research Maatschapp B.V. | High pressure compressor lubrication |
| EP2626405B1 (fr) | 2012-02-10 | 2015-05-27 | Ab Nanol Technologies Oy | Composition lubrifiante |
| JP5872946B2 (ja) * | 2012-03-30 | 2016-03-01 | 出光興産株式会社 | 潤滑油組成物 |
| JP5552139B2 (ja) * | 2012-05-23 | 2014-07-16 | Ｊｘ日鉱日石エネルギー株式会社 | 潤滑油基油、潤滑油組成物及び潤滑油基油の製造方法 |
| WO2013189951A1 (fr) | 2012-06-21 | 2013-12-27 | Shell Internationale Research Maatschappij B.V. | Composition de lubrification |
| EP2883946B1 (fr) * | 2012-07-31 | 2019-06-12 | Idemitsu Kosan Co., Ltd | Composition lubrifiante pour un moteur à combustion interne |
| RU2638441C2 (ru) | 2012-08-01 | 2017-12-15 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Композиция наполнителя кабеля |
| EP2695932A1 (fr) | 2012-08-08 | 2014-02-12 | Ab Nanol Technologies Oy | Composition de graisse |
| EP2816097A1 (fr) | 2013-06-18 | 2014-12-24 | Shell Internationale Research Maatschappij B.V. | Composition d'huile de lubrification |
| EP2816098A1 (fr) | 2013-06-18 | 2014-12-24 | Shell Internationale Research Maatschappij B.V. | Utilisation d'un composé à soufre pour améliorer la stabilité oxidante d'une composition d'huile de lubrification |
| BR112016015027B1 (pt) | 2013-12-24 | 2021-04-27 | Shell Internationale Research Maatschappij B.V. | Composição lubrificante e uso da mesma |
| KR101814320B1 (ko) | 2014-03-28 | 2018-01-02 | 미쓰이 가가쿠 가부시키가이샤 | 에틸렌/α-올레핀 공중합체 및 윤활유 |
| US8968592B1 (en) | 2014-04-10 | 2015-03-03 | Soilworks, LLC | Dust suppression composition and method of controlling dust |
| US9068106B1 (en) | 2014-04-10 | 2015-06-30 | Soilworks, LLC | Dust suppression composition and method of controlling dust |
| CN115093893A (zh) * | 2014-04-25 | 2022-09-23 | 路博润公司 | 多级润滑组合物 |
| WO2015172846A1 (fr) | 2014-05-16 | 2015-11-19 | Ab Nanol Technologies Oy | Composition d'additif pour lubrifiants |
| JP2017518426A (ja) | 2014-06-19 | 2017-07-06 | 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 | 潤滑組成物 |
| WO2016032782A1 (fr) | 2014-08-27 | 2016-03-03 | Shell Oil Company | Procédés de lubrification d'une surface revêtue de carbone de type diamant, compositions d'huile lubrifiante associées et procédés de criblage associés |
| KR101970078B1 (ko) | 2014-09-10 | 2019-04-17 | 미쓰이 가가쿠 가부시키가이샤 | 윤활유 조성물 |
| CN104357159A (zh) * | 2014-09-26 | 2015-02-18 | 苏州长盛机电有限公司 | 机械传动件用可降解润滑剂及其制备方法 |
| KR20160044306A (ko) * | 2014-10-15 | 2016-04-25 | 현대자동차주식회사 | 연비 및 내구향상형 디젤엔진오일 조성물 |
| JP6812345B2 (ja) | 2014-11-04 | 2021-01-13 | 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 | 潤滑用組成物 |
| 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 |
| BR112017016838B1 (pt) | 2015-02-06 | 2021-05-11 | Shell Internationale Research Maatschappij B.V | composição de graxa e uso da referida composição |
| US20180037838A1 (en) | 2015-02-27 | 2018-02-08 | Shell Oil Company | Use of a lubricating composition |
| WO2016156328A1 (fr) | 2015-03-31 | 2016-10-06 | Shell Internationale Research Maatschappij B.V. | Utilisation d'une composition lubrifiante comprenant un photostabilisant de type amine encombrée pour une meilleure propreté d'un piston dans un moteur à combustion interne |
| WO2016166135A1 (fr) | 2015-04-15 | 2016-10-20 | Shell Internationale Research Maatschappij B.V. | Procédé permettant de détecter la présence d'hydrocarbures obtenus à partir du méthane dans un mélange |
| WO2016184842A1 (fr) | 2015-05-18 | 2016-11-24 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| US9434881B1 (en) | 2015-08-25 | 2016-09-06 | Soilworks, LLC | Synthetic fluids as compaction aids |
| KR101755889B1 (ko) * | 2015-11-19 | 2017-07-19 | 현대자동차주식회사 | 연비 및 내구성이 향상된 디젤 엔진오일 조성물 |
| RU2604065C1 (ru) * | 2015-11-27 | 2016-12-10 | федеральное государственное автономное образовательное учреждение высшего образования "Южный федеральный университет" | Смазочная композиция |
| CN109071736B (zh) | 2016-05-13 | 2021-08-10 | 赢创运营有限公司 | 基于聚烯烃主链和甲基丙烯酸酯侧链的接枝共聚物 |
| CA3033901A1 (fr) | 2016-08-15 | 2018-02-22 | Evonik Oil Additives Gmbh | Polyalkyle (meth)acrylates fonctionnels ayant une performance de desemulsibilite amelioree |
| CA3034737A1 (fr) | 2016-08-31 | 2018-03-08 | Evonik Oil Additives Gmbh | Polymeres en peigne permettant d'ameliorer la perte par evaporation selon noack de formulations d'huile pour moteur |
| EP3336162A1 (fr) | 2016-12-16 | 2018-06-20 | Shell International Research Maatschappij B.V. | Composition de lubrification |
| US10941368B2 (en) | 2016-12-19 | 2021-03-09 | Evonik Operations Gmbh | Lubricating oil composition comprising dispersant comb polymers |
| KR102208021B1 (ko) | 2017-01-16 | 2021-01-26 | 미쓰이 가가쿠 가부시키가이샤 | 자동차 기어용 윤활유 조성물 |
| CN110621768B (zh) * | 2017-03-24 | 2023-02-21 | 埃克森美孚化学专利公司 | 冷起动模拟机粘度提升基料和含有它们的润滑油制剂 |
| US20180305633A1 (en) | 2017-04-19 | 2018-10-25 | Shell Oil Company | Lubricating compositions comprising a volatility reducing additive |
| BR112019022507B1 (pt) | 2017-04-27 | 2022-12-13 | Shell Internationale Research Maatschappij B.V. | Uso de um dispersante sem cinzas contendo nitrogênio em uma composição lubrificante |
| DK3668949T3 (da) * | 2017-06-19 | 2022-04-04 | Neste Oyj | TIO2-katalysator i ketoniseringsreaktioner til fremstilling af fornyelig basisolie |
| WO2019012031A1 (fr) | 2017-07-14 | 2019-01-17 | Evonik Oil Additives Gmbh | Polymères en peigne à fonctionnalité imide |
| EP3450527B1 (fr) | 2017-09-04 | 2020-12-02 | Evonik Operations GmbH | Nouveaux améliorants l'indice de viscosité ayant des répartitions de poids moléculaire définies |
| ES2801327T3 (es) | 2017-12-13 | 2021-01-11 | Evonik Operations Gmbh | Mejorador del índice de viscosidad con resistencia al cizallamiento y solubilidad después del cizallamiento mejoradas |
| US11198833B2 (en) | 2018-01-23 | 2021-12-14 | Evonik Operations Gmbh | Polymeric-inorganic nanoparticle compositions, manufacturing process thereof and their use as lubricant additives |
| KR102587267B1 (ko) | 2018-01-23 | 2023-10-11 | 에보닉 오퍼레이션스 게엠베하 | 중합체-무기 나노입자 조성물, 이의 제조 방법 및 윤활제 첨가제로서의 이들의 용도 |
| WO2019145287A1 (fr) | 2018-01-23 | 2019-08-01 | Evonik Oil Additives Gmbh | Compositions nanoparticulaires polymères inorganiques, leur procédé de fabrication et leur utilisation en tant qu'additifs pour lubrifiants |
| US11591539B2 (en) | 2018-04-26 | 2023-02-28 | Shell Usa, Inc. | Lubricant composition and use of the same as a pipe dope |
| EP3788122B1 (fr) * | 2018-05-01 | 2023-09-27 | Novvi LLC | Mélange d'hydrocarbures présentant une structure de ramification unique |
| WO2020007945A1 (fr) | 2018-07-05 | 2020-01-09 | Shell Internationale Research Maatschappij B.V. | Composition lubrifiante |
| CN112384599B (zh) | 2018-07-13 | 2023-05-30 | 国际壳牌研究有限公司 | 润滑组合物 |
| WO2020064619A1 (fr) | 2018-09-24 | 2020-04-02 | Evonik Operations Gmbh | Utilisation de composés à base de trialcoxysilane pour lubrifiants |
| JP7459087B2 (ja) | 2018-11-13 | 2024-04-01 | エボニック オペレーションズ ゲーエムベーハー | 基油または潤滑剤添加剤として使用するためのランダムコポリマー |
| EP3898721B1 (fr) | 2018-12-19 | 2023-05-03 | Evonik Operations GmbH | Dispositifs d'amélioration de l'indice de viscosité basés sur des copolymères séquencés |
| EP3898907A1 (fr) | 2018-12-19 | 2021-10-27 | Evonik Operations GmbH | Utilisation de copolymères triséquencés associatifs en tant qu'agents d'amélioration de l'indice de viscosité |
| CA3075112C (fr) | 2019-03-11 | 2023-12-19 | Evonik Operations Gmbh | Copolymeres a base de polyalkyle methacrylate et utilisation comme ameliorants de l'indice de viscosite |
| SG11202110027XA (en) | 2019-03-20 | 2021-10-28 | Evonik Operations Gmbh | Polyalkyl(meth)acrylates for improving fuel economy, dispersancy and deposits performance |
| KR20210139403A (ko) | 2019-03-26 | 2021-11-22 | 미쓰이 가가쿠 가부시키가이샤 | 공업 기어용 윤활유 조성물 및 그의 제조 방법 |
| EP3950901A4 (fr) | 2019-03-26 | 2022-08-17 | Mitsui Chemicals, Inc. | Composition d'huile lubrifmposition d'huile lubrifiante pour moteur à combustion interne, et procédé de fabrication de celle-ci |
| KR20210139407A (ko) | 2019-03-26 | 2021-11-22 | 미쓰이 가가쿠 가부시키가이샤 | 그리스 조성물 및 그의 제조 방법 |
| KR20210139400A (ko) | 2019-03-26 | 2021-11-22 | 미쓰이 가가쿠 가부시키가이샤 | 자동차 기어용 윤활유 조성물 및 그의 제조 방법 |
| CN113574150A (zh) | 2019-03-26 | 2021-10-29 | 三井化学株式会社 | 汽车变速箱油用润滑油组合物及其制造方法 |
| CN113574148A (zh) | 2019-03-26 | 2021-10-29 | 三井化学株式会社 | 内燃机用润滑油组合物及其制造方法 |
| US20220169948A1 (en) | 2019-03-26 | 2022-06-02 | Mitsui Chemicals, Inc. | Lubricating oil composition for compressor oils and method for producing the same |
| EP3950895A4 (fr) | 2019-03-26 | 2022-08-10 | Mitsui Chemicals, Inc. | Composition d'huile lubrifiante pour huile de fonctionnement, et procédé de fabrication de celle-ci |
| EP3778839B1 (fr) | 2019-08-13 | 2021-08-04 | Evonik Operations GmbH | Agent améliorant l'indice de viscosité présentant une meilleure résistance au cisaillement |
| JP7408344B2 (ja) | 2019-10-23 | 2024-01-05 | シェルルブリカンツジャパン株式会社 | 潤滑油組成物 |
| CN111122637B (zh) * | 2020-03-27 | 2020-07-07 | 南京昊绿生物科技有限公司 | 基于核磁共振定量碳谱分析的生物油中c、h、o含量计算方法 |
| EP4127115B1 (fr) | 2020-03-30 | 2023-11-15 | Shell Internationale Research Maatschappij B.V. | Système de gestion thermique |
| WO2021197974A1 (fr) | 2020-03-30 | 2021-10-07 | Shell Internationale Research Maatschappij B.V. | Gestion d'emballement thermique |
| EP4143280B1 (fr) | 2020-04-30 | 2023-11-29 | Evonik Operations GmbH | Procédé pour la préparation de polymères polyalkyl (méth)acrylate |
| EP4143279B1 (fr) | 2020-04-30 | 2024-06-26 | Evonik Operations GmbH | Procédé pour la préparation de polymères poly(méth)acrylates d'alkyle dispersants |
| PL3907269T3 (pl) | 2020-05-05 | 2023-09-11 | Evonik Operations Gmbh | Uwodornione polidienowe kopolimery liniowe jako surowiec bazowy lub dodatki smarowe do kompozycji smarowych |
| CN111575082B (zh) * | 2020-06-16 | 2021-09-07 | 烟台德高石油有限公司 | 一种新能源车载滑片式空气压缩机用压缩机油及其制备方法 |
| ES2980905T3 (es) | 2020-07-03 | 2024-10-03 | Evonik Operations Gmbh | Fluidos base de alta viscosidad basados en poliésteres compatibles con el petróleo |
| EP4176026B1 (fr) | 2020-07-03 | 2024-03-06 | Evonik Operations GmbH | Fluides de base à haute viscosité à base de polyesters compatibles avec l'huile préparés à partir d'époxydes à longue chaîne |
| US12104137B2 (en) | 2020-09-01 | 2024-10-01 | Shell Usa, Inc. | Engine oil composition |
| US20240034855A1 (en) | 2020-09-18 | 2024-02-01 | Evonik Operations Gmbh | Compositions comprising a graphene-based material as lubricant additives |
| EP4247923B1 (fr) | 2020-11-18 | 2024-08-07 | Evonik Operations GmbH | Huiles pour compresseurs à indice de viscosité élevé |
| CA3202022A1 (fr) | 2020-12-18 | 2022-06-23 | Evonik Operations Gmbh | Procede de preparation d'homo polymeres et de copolymeres de (meth)acrylates d'alkyle ayant une faible teneur en monomeres residuels |
| EP4060009B1 (fr) | 2021-03-19 | 2023-05-03 | Evonik Operations GmbH | Un agent améliorant l'indice de viscosité et composition lubrifiante |
| EP4119640B1 (fr) | 2021-07-16 | 2023-06-14 | Evonik Operations GmbH | Composition d'additif lubrifiant contenant des polyalkyl méthacrylates |
| WO2023002947A1 (fr) | 2021-07-20 | 2023-01-26 | 三井化学株式会社 | Modificateur de viscosité pour huile lubrifiante, et composition d'huile lubrifiante pour huile hydraulique |
| WO2023099635A1 (fr) | 2021-12-03 | 2023-06-08 | Totalenergies Onetech | Compositions lubrifiantes |
| EP4441180A1 (fr) | 2021-12-03 | 2024-10-09 | TotalEnergies OneTech | Compositions lubrifiantes |
| EP4441178A1 (fr) | 2021-12-03 | 2024-10-09 | TotalEnergies OneTech | Compositions lubrifiantes |
| EP4441176A1 (fr) | 2021-12-03 | 2024-10-09 | Evonik Operations GmbH | Polymères de poly(méth)acrylate d'alkyle modifiés par un ester boronique |
| EP4441175A1 (fr) | 2021-12-03 | 2024-10-09 | Evonik Operations GmbH | Polymères de polyalkyl(méth)acrylate modifiés par un ester boronique |
| WO2023099632A1 (fr) | 2021-12-03 | 2023-06-08 | Evonik Operations Gmbh | Polymères de poly(méth)acrylate d'alkyle modifiés par un ester boronique |
| KR20240137667A (ko) | 2022-03-03 | 2024-09-20 | 미쓰이 가가쿠 가부시키가이샤 | 윤활유 조성물 |
| WO2023222677A1 (fr) | 2022-05-19 | 2023-11-23 | Shell Internationale Research Maatschappij B.V. | Système de gestion thermique |
| WO2024033156A1 (fr) | 2022-08-08 | 2024-02-15 | Evonik Operations Gmbh | Polymères à base de polyalkyle (méth)acrylate présentant des propriétés à basse température améliorées |
| EP4321602B1 (fr) | 2022-08-10 | 2024-09-11 | Evonik Operations GmbH | Copolymères de poly(méth)acrylate d'alkyle sans soufre utilisés comme améliorants d'indice de viscosité dans des lubrifiants |
| WO2024120926A1 (fr) | 2022-12-07 | 2024-06-13 | Evonik Operations Gmbh | Polymères dispersants exempts de soufre pour applications industrielles |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4500417A (en) | 1982-12-28 | 1985-02-19 | Mobil Oil Corporation | Conversion of Fischer-Tropsch products |
| DE3678024D1 (de) | 1985-03-26 | 1991-04-18 | Mitsui Petrochemical Ind | Fluessiges statisches ethylencopolymer, verfahren zur herstellung und anwendung desselben. |
| US4827064A (en) | 1986-12-24 | 1989-05-02 | Mobil Oil Corporation | High viscosity index synthetic lubricant compositions |
| US4992183A (en) | 1987-04-01 | 1991-02-12 | Ethyl Corporation | Multigrade hydrogenated decene-1 oligomer engine oils |
| US4943672A (en) | 1987-12-18 | 1990-07-24 | Exxon Research And Engineering Company | Process for the hydroisomerization of Fischer-Tropsch wax to produce lubricating oil (OP-3403) |
| US5059299A (en) | 1987-12-18 | 1991-10-22 | Exxon Research And Engineering Company | Method for isomerizing wax to lube base oils |
| FR2626005A1 (fr) | 1988-01-14 | 1989-07-21 | Shell Int Research | Procede de preparation d'une huile lubrifiante de base |
| DK0458895T3 (da) | 1989-02-17 | 1995-11-06 | Chevron Usa Inc | Isomerisering af voksagtige smøreolier og jordolievoks under anvendelse af en silicoaluminophosphat-molsi-katalysator |
| US5246566A (en) | 1989-02-17 | 1993-09-21 | Chevron Research And Technology Company | Wax isomerization using catalyst of specific pore geometry |
| US5282958A (en) | 1990-07-20 | 1994-02-01 | Chevron Research And Technology Company | Use of modified 5-7 a pore molecular sieves for isomerization of hydrocarbons |
| DE69013905T3 (de) | 1990-07-24 | 2005-06-02 | Ethyl Petroleum Additives Ltd., Bracknell | Biologisch abbaubare Schmieröle und funktionelle Flüssigkeiten. |
| US5107054A (en) | 1990-08-23 | 1992-04-21 | Mobil Oil Corporation | Zeolite MCM-22 based catalyst for paraffin isomerization |
| FR2675812B1 (fr) | 1991-04-26 | 1993-08-13 | Bp France | Procede de preparation d'huiles de base et de cires liquides biodegradables, nouveaux produits lubrifiants biodegradables obtenus. |
| FR2676749B1 (fr) | 1991-05-21 | 1993-08-20 | Inst Francais Du Petrole | Procede d'hydroisomerisation de paraffines issues du procede fischer-tropsch a l'aide de catalyseurs a base de zeolithe h-y. |
| JPH0586389A (ja) | 1991-09-27 | 1993-04-06 | Showa Shell Sekiyu Kk | 生分解性グリース組成物 |
| GB9201338D0 (en) | 1992-01-22 | 1992-03-11 | British Petroleum Co Plc | Lubricating oil compositions |
| ES2158843T3 (es) | 1992-01-30 | 2001-09-16 | Bp Amoco Corp | Lubricantes y fluidos funcionales biodegradables. |
| DE4217961A1 (de) | 1992-05-30 | 1993-12-02 | Fuchs Petrolub Ag Oel & Chemie | Umweltverträgliche und biologisch schnell aubbaubare Betriebsstoffe zur Umlaufschmierung von Motoren und sonstigen Aggregaten in Fahrzeugen und Arbeitsmaschinen |
| US5362378A (en) | 1992-12-17 | 1994-11-08 | Mobil Oil Corporation | Conversion of Fischer-Tropsch heavy end products with platinum/boron-zeolite beta catalyst having a low alpha value |
| EP0607553B1 (fr) | 1993-01-09 | 1997-06-04 | Hüls Aktiengesellschaft | Utilisation de polyméthylalcanes comme huiles de base biodégradables dans des lubrifiants et des fluides fonctionnels |
| US6093861A (en) * | 1993-01-25 | 2000-07-25 | Muntz; Pieter Jan Dirk | Lubricating oil composition |
| US5663126A (en) | 1994-10-21 | 1997-09-02 | Castrol Limited | Polar grafted polyolefins, methods for their manufacture, and lubricating oil compositions containing them |
| US5789355A (en) | 1995-06-06 | 1998-08-04 | Exxon Chemical Limited | Low volatility lubricating compositions |
| EP1365005B1 (fr) | 1995-11-28 | 2005-10-19 | Shell Internationale Researchmaatschappij B.V. | Procédé pour la production d'huiles lubrifiantes |
| BR9611898A (pt) | 1995-12-08 | 2000-05-16 | Exxon Research Engineering Co | Processo para a produção de um óleo de base de hidrocarboneto biodegradável de alto desempenho, e, respectivo óleo |
| US5833839A (en) | 1995-12-08 | 1998-11-10 | Exxon Research And Engineering Company | High purity paraffinic solvent compositions, and process for their manufacture |
| US6090989A (en) | 1997-10-20 | 2000-07-18 | Mobil Oil Corporation | Isoparaffinic lube basestock compositions |
| MA25044A1 (fr) * | 1997-10-23 | 2000-10-01 | Procter & Gamble | Compositions de lavage contenant des variants de proteases multisubstituees. |
| US6059955A (en) | 1998-02-13 | 2000-05-09 | Exxon Research And Engineering Co. | Low viscosity lube basestock |
| US6008164A (en) | 1998-08-04 | 1999-12-28 | Exxon Research And Engineering Company | Lubricant base oil having improved oxidative stability |
| US6080301A (en) | 1998-09-04 | 2000-06-27 | Exxonmobil Research And Engineering Company | Premium synthetic lubricant base stock having at least 95% non-cyclic isoparaffins |
-
2000
- 2000-02-04 US US09/498,793 patent/US7067049B1/en not_active Expired - Fee Related
-
2001
- 2001-01-26 EP EP01949000A patent/EP1252279A1/fr not_active Withdrawn
- 2001-01-26 JP JP2001557985A patent/JP2003528169A/ja active Pending
- 2001-01-26 WO PCT/US2001/002645 patent/WO2001057166A1/fr active IP Right Grant
- 2001-01-26 BR BR0107986-7A patent/BR0107986A/pt not_active Application Discontinuation
- 2001-01-26 MX MXPA02007524A patent/MXPA02007524A/es active IP Right Grant
- 2001-01-26 CN CN01804531A patent/CN1398292A/zh active Pending
- 2001-01-26 CA CA2399489A patent/CA2399489C/fr not_active Expired - Fee Related
- 2001-01-26 AU AU29776/01A patent/AU777201B2/en not_active Ceased
- 2001-01-26 KR KR1020027009921A patent/KR20020074226A/ko not_active Application Discontinuation
- 2001-01-26 RU RU2002123583/04A patent/RU2247141C2/ru not_active IP Right Cessation
- 2001-02-02 TW TW090102195A patent/TW585907B/zh not_active IP Right Cessation
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| Publication number | Publication date |
|---|---|
| RU2247141C2 (ru) | 2005-02-27 |
| NO20023676D0 (no) | 2002-08-02 |
| NO20023676L (no) | 2002-10-04 |
| EP1252279A1 (fr) | 2002-10-30 |
| CA2399489C (fr) | 2010-04-13 |
| US7067049B1 (en) | 2006-06-27 |
| RU2002123583A (ru) | 2004-01-10 |
| CN1398292A (zh) | 2003-02-19 |
| AU2977601A (en) | 2001-08-14 |
| TW585907B (en) | 2004-05-01 |
| BR0107986A (pt) | 2002-10-22 |
| KR20020074226A (ko) | 2002-09-28 |
| AU777201B2 (en) | 2004-10-07 |
| AR027363A1 (es) | 2003-03-26 |
| MXPA02007524A (es) | 2003-01-28 |
| CA2399489A1 (fr) | 2001-08-09 |
| WO2001057166A1 (fr) | 2001-08-09 |
| JP2003528169A (ja) | 2003-09-24 |
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