BRPI0710256A2 - composição de óleo lubrificante; composição concentrada de aditivo de óleo lubrificante, composição de óleo de motor; composição concentrada de aditivo de óleo de motor; e método de aumentar a concetração de pelo menos um antioxidante fenólico impedido em uma composição concentrada de aditivo de óleo lubrificante - Google Patents

composição de óleo lubrificante; composição concentrada de aditivo de óleo lubrificante, composição de óleo de motor; composição concentrada de aditivo de óleo de motor; e método de aumentar a concetração de pelo menos um antioxidante fenólico impedido em uma composição concentrada de aditivo de óleo lubrificante Download PDF

Info

Publication number: BRPI0710256A2
Authority: BR; Brazil
Prior art keywords: lubricating oil; composition according; formula; boronated; hindered
Prior art date: 2006-03-29

Application number

BRPI0710256-9A

Other languages

English (en)

Portuguese (pt)

Inventor

Vicent J Gatto

Emily R Scheller

William E Moehle

Original Assignee

Albermarle Corp

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

2006-03-29

Filing date

2007-03-28

Publication date

2011-08-09

2007-03-28 Application filed by Albermarle Corp filed Critical Albermarle Corp

2011-08-09 Publication of BRPI0710256A2 publication Critical patent/BRPI0710256A2/pt

Links

239000000203 mixture Substances 0.000 title claims abstract description 104
239000010687 lubricating oil Substances 0.000 title claims abstract description 67
239000002530 phenolic antioxidant Substances 0.000 title claims abstract description 57
239000000654 additive Substances 0.000 title claims abstract description 43
230000000996 additive effect Effects 0.000 title claims abstract description 40
239000010705 motor oil Substances 0.000 title claims abstract description 32
238000000034 method Methods 0.000 title claims abstract description 15
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical class C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims abstract description 88
150000001875 compounds Chemical class 0.000 claims abstract description 80
239000002272 engine oil additive Substances 0.000 claims abstract description 3
235000013824 polyphenols Nutrition 0.000 claims description 66
239000003921 oil Substances 0.000 claims description 39
229910052750 molybdenum Inorganic materials 0.000 claims description 34
239000011733 molybdenum Substances 0.000 claims description 32
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 29
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 27
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 27
229910052717 sulfur Inorganic materials 0.000 claims description 26
239000011593 sulfur Substances 0.000 claims description 26
DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 claims description 18
125000000217 alkyl group Chemical group 0.000 claims description 16
239000003963 antioxidant agent Substances 0.000 claims description 14
125000004122 cyclic group Chemical group 0.000 claims description 9
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 8
229910052796 boron Inorganic materials 0.000 claims description 8
KHYKFSXXGRUKRE-UHFFFAOYSA-J molybdenum(4+) tetracarbamodithioate Chemical compound C(N)([S-])=S.[Mo+4].C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S KHYKFSXXGRUKRE-UHFFFAOYSA-J 0.000 claims description 8
MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical group CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 claims description 7
230000003078 antioxidant effect Effects 0.000 claims description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
239000003085 diluting agent Substances 0.000 claims description 7
229910052760 oxygen Inorganic materials 0.000 claims description 7
239000001301 oxygen Substances 0.000 claims description 7
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
239000005078 molybdenum compound Substances 0.000 claims description 4
239000003345 natural gas Substances 0.000 claims description 3
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 claims description 3
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 claims description 2
150000002894 organic compounds Chemical class 0.000 claims description 2
150000002989 phenols Chemical class 0.000 claims description 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000005621 boronate group Chemical class 0.000 claims 1
239000000314 lubricant Substances 0.000 abstract description 14
230000001590 oxidative effect Effects 0.000 abstract description 10
230000002195 synergetic effect Effects 0.000 abstract description 4
230000002939 deleterious effect Effects 0.000 abstract description 2
-1 3,3-dimethylbutyl Chemical group 0.000 description 31
230000003647 oxidation Effects 0.000 description 14
238000007254 oxidation reaction Methods 0.000 description 14
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 9
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 8
229910052698 phosphorus Inorganic materials 0.000 description 8
239000011574 phosphorus Substances 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 6
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 6
239000003599 detergent Substances 0.000 description 5
229910017464 nitrogen compound Inorganic materials 0.000 description 5
150000002830 nitrogen compounds Chemical class 0.000 description 5
150000003335 secondary amines Chemical class 0.000 description 5
ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 4
229910052783 alkali metal Inorganic materials 0.000 description 4
150000001340 alkali metals Chemical class 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
239000002585 base Substances 0.000 description 4
239000011575 calcium Substances 0.000 description 4
229910052791 calcium Inorganic materials 0.000 description 4
150000004985 diamines Chemical class 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
239000010685 fatty oil Substances 0.000 description 4
239000003112 inhibitor Substances 0.000 description 4
229910052742 iron Inorganic materials 0.000 description 4
239000002253 acid Substances 0.000 description 3
125000003158 alcohol group Chemical group 0.000 description 3
125000005263 alkylenediamine group Chemical group 0.000 description 3
239000002199 base oil Substances 0.000 description 3
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 3
CBDHDQAONYJJIJ-UHFFFAOYSA-N di(butan-2-yloxy)borinic acid Chemical compound CCC(C)OB(O)OC(C)CC CBDHDQAONYJJIJ-UHFFFAOYSA-N 0.000 description 3
239000012990 dithiocarbamate Substances 0.000 description 3
239000012530 fluid Substances 0.000 description 3
230000006698 induction Effects 0.000 description 3
239000003607 modifier Substances 0.000 description 3
150000002752 molybdenum compounds Chemical class 0.000 description 3
239000010723 turbine oil Substances 0.000 description 3
239000004711 α-olefin Substances 0.000 description 3
QVXGKJYMVLJYCL-UHFFFAOYSA-N 2,3-di(nonyl)-N-phenylaniline Chemical compound C(CCCCCCCC)C=1C(=C(C=CC1)NC1=CC=CC=C1)CCCCCCCCC QVXGKJYMVLJYCL-UHFFFAOYSA-N 0.000 description 2
JERZAOOJWPHIDG-UHFFFAOYSA-N 2,4-di(butan-2-yl)phenol Chemical compound CCC(C)C1=CC=C(O)C(C(C)CC)=C1 JERZAOOJWPHIDG-UHFFFAOYSA-N 0.000 description 2
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
BKZXZGWHTRCFPX-UHFFFAOYSA-N 2-tert-butyl-6-methylphenol Chemical compound CC1=CC=CC(C(C)(C)C)=C1O BKZXZGWHTRCFPX-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
239000004322 Butylated hydroxytoluene Substances 0.000 description 2
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 2
235000018660 ammonium molybdate Nutrition 0.000 description 2
239000011609 ammonium molybdate Substances 0.000 description 2
229940010552 ammonium molybdate Drugs 0.000 description 2
239000007866 anti-wear additive Substances 0.000 description 2
230000005540 biological transmission Effects 0.000 description 2
229940095259 butylated hydroxytoluene Drugs 0.000 description 2
235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
238000007707 calorimetry Methods 0.000 description 2
QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
230000002498 deadly effect Effects 0.000 description 2
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
150000002009 diols Chemical class 0.000 description 2
QXYJCZRRLLQGCR-UHFFFAOYSA-N dioxomolybdenum Chemical compound O=[Mo]=O QXYJCZRRLLQGCR-UHFFFAOYSA-N 0.000 description 2
239000003623 enhancer Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
239000003879 lubricant additive Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 2
LVZUNTGFCXNQAF-UHFFFAOYSA-N n-nonyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(CCCCCCCCC)C1=CC=CC=C1 LVZUNTGFCXNQAF-UHFFFAOYSA-N 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920000768 polyamine Polymers 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
239000011591 potassium Substances 0.000 description 2
235000007686 potassium Nutrition 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
OLBCVFGFOZPWHH-UHFFFAOYSA-N propofol Chemical compound CC(C)C1=CC=CC(C(C)C)=C1O OLBCVFGFOZPWHH-UHFFFAOYSA-N 0.000 description 2
235000015393 sodium molybdate Nutrition 0.000 description 2
239000011684 sodium molybdate Substances 0.000 description 2
TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 2
229910052725 zinc Inorganic materials 0.000 description 2
239000011701 zinc Substances 0.000 description 2
KUHJJSKJQLIHBS-UHFFFAOYSA-N 1,4-diaminobutan-1-ol Chemical compound NCCCC(N)O KUHJJSKJQLIHBS-UHFFFAOYSA-N 0.000 description 1
125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000004398 2-methyl-2-butyl group Chemical group CC(C)(CC)* 0.000 description 1
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
125000005916 2-methylpentyl group Chemical group 0.000 description 1
QEYMMOKECZBKAC-UHFFFAOYSA-N 3-chloropropanoic acid Chemical compound OC(=O)CCCl QEYMMOKECZBKAC-UHFFFAOYSA-N 0.000 description 1
125000004917 3-methyl-2-butyl group Chemical group CC(C(C)*)C 0.000 description 1
125000004919 3-methyl-2-pentyl group Chemical group CC(C(C)*)CC 0.000 description 1
125000004921 3-methyl-3-pentyl group Chemical group CC(CC)(CC)* 0.000 description 1
125000005917 3-methylpentyl group Chemical group 0.000 description 1
125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
239000005069 Extreme pressure additive Substances 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
MJOQJPYNENPSSS-XQHKEYJVSA-N [(3r,4s,5r,6s)-4,5,6-triacetyloxyoxan-3-yl] acetate Chemical compound CC(=O)O[C@@H]1CO[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O MJOQJPYNENPSSS-XQHKEYJVSA-N 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-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
230000015556 catabolic process Effects 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000010725 compressor oil Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
ZKKLPDLKUGTPME-UHFFFAOYSA-N diazanium;bis(sulfanylidene)molybdenum;sulfanide Chemical compound [NH4+].[NH4+].[SH-].[SH-].S=[Mo]=S ZKKLPDLKUGTPME-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
229910001882 dioxygen Inorganic materials 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000012208 gear oil Substances 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
239000004519 grease Substances 0.000 description 1
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
238000004128 high performance liquid chromatography Methods 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
239000010722 industrial gear oil Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 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
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
125000001741 organic sulfur group Chemical group 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
229920013639 polyalphaolefin Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910052979 sodium sulfide Inorganic materials 0.000 description 1
GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000010736 steam turbine oil Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
PTISTKLWEJDJID-UHFFFAOYSA-N sulfanylidenemolybdenum Chemical compound [Mo]=S PTISTKLWEJDJID-UHFFFAOYSA-N 0.000 description 1
230000008961 swelling Effects 0.000 description 1
238000010998 test method Methods 0.000 description 1
CXVCSRUYMINUSF-UHFFFAOYSA-N tetrathiomolybdate(2-) Chemical compound [S-][Mo]([S-])(=S)=S CXVCSRUYMINUSF-UHFFFAOYSA-N 0.000 description 1
230000008719 thickening Effects 0.000 description 1
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/12—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic compound containing atoms of elements not provided for in groups C10M141/02 - C10M141/10
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
- C10M2219/068—Thiocarbamate metal 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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/252—Diesel engines
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/14—Chemical after-treatment of the constituents of the lubricating composition by boron or a compound containing boron

Landscapes

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

BRPI0710256-9A 2006-03-29 2007-03-28 composição de óleo lubrificante; composição concentrada de aditivo de óleo lubrificante, composição de óleo de motor; composição concentrada de aditivo de óleo de motor; e método de aumentar a concetração de pelo menos um antioxidante fenólico impedido em uma composição concentrada de aditivo de óleo lubrificante BRPI0710256A2 (pt)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
US78733406P	2006-03-29	2006-03-29
US60/787,334		2006-03-29
PCT/US2007/065371 WO2007115042A2 (fr)	2006-03-29	2007-03-28	Compositions d'additifs pour huiles lubrifiantes

Publications (1)

Publication Number	Publication Date
BRPI0710256A2 true BRPI0710256A2 (pt)	2011-08-09

Family

ID=37110316

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BRPI0710256-9A BRPI0710256A2 (pt)	2006-03-29	2007-03-28	composição de óleo lubrificante; composição concentrada de aditivo de óleo lubrificante, composição de óleo de motor; composição concentrada de aditivo de óleo de motor; e método de aumentar a concetração de pelo menos um antioxidante fenólico impedido em uma composição concentrada de aditivo de óleo lubrificante

Country Status (11)

Country	Link
US (1)	US20100286004A1 (fr)
EP (1)	EP2004780A2 (fr)
JP (1)	JP2009531533A (fr)
KR (1)	KR20080103588A (fr)
CN (1)	CN101415805A (fr)
AU (1)	AU2007233234A1 (fr)
BR (1)	BRPI0710256A2 (fr)
CA (1)	CA2647574A1 (fr)
EA (1)	EA200870386A1 (fr)
TW (1)	TW200801174A (fr)
WO (1)	WO2007115042A2 (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7897552B2 (en) *	2007-11-30	2011-03-01	Afton Chemical Corporation	Additives and lubricant formulations for improved antioxidant properties
US8748357B2 (en) *	2008-07-15	2014-06-10	Exxonmobil Research And Engineering Company	Method for stabilizing diesel engine lubricating oil against degradation by biodiesel fuel
US20100152074A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
US20100152072A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
US20100152073A1 (en)	2008-12-17	2010-06-17	Chevron Oronite Company Llc	Lubricating oil compositions
EP2550346B1 (fr)	2010-03-25	2020-11-04	Vanderbilt Chemicals, LLC	Compositions lubrifiantes à ultrabasse teneur en phosphore
US8334242B2 (en) *	2010-10-12	2012-12-18	Chevron Oronite Company Llc	Lubricating composition containing multifunctional borated hydroxylated amine salt of a hindered phenolic acid
CA2838465C (fr) *	2011-06-17	2020-01-07	Biosynthetic Technologies, Llc	Compositions d'estolide presentant une stabilite oxydante elevee
KR101974660B1 (ko) *	2013-04-26	2019-05-02	에스케이이노베이션 주식회사	산화 안정성 및 색상안정성이 우수한 윤활유 조성물
CN104345085A (zh) *	2013-08-01	2015-02-11	中国石油化工股份有限公司	电解液及其用途
FR3032710B1 (fr) *	2015-02-17	2018-06-22	Compagnie Generale Des Etablissements Michelin	Pneumatique dont la bande de roulement comporte un compose phenolique
GB2579405B (en)	2018-11-30	2022-09-14	Si Group Switzerland Chaa Gmbh	Antioxidant compositions
US12606769B2 (en)	2019-03-22	2026-04-21	Chevron Oronite Company Llc	Antioxidants with high mono-alkylated diphenylamine content
WO2021181286A1 (fr) *	2020-03-11	2021-09-16	Chevron Oronite Company Llc	Compositions d'huile lubrifiante ayant une performance oxydative améliorée comprenant un antioxydant de diphénylamine alkylée et des détergents à base de sulfonate
CN116601263B (zh) *	2020-11-17	2025-07-01	松原实业有限公司	性能提高的包含烷基化二苯胺的组合物

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL122614C (fr) *	1961-09-25
EP0089844B1 (fr) *	1982-03-22	1985-12-04	Ethyl Corporation	Esters de bore, leur préparation et emploi comme antioxydant
US4927553A (en) *	1983-05-06	1990-05-22	Ethyl Corporation	Haze-free boronated antioxidant
GB9318928D0 (en) *	1993-09-13	1993-10-27	Exxon Research Engineering Co	Lubricant composition containing combination of antiwear and antioxidant additives
KR100239817B1 (ko) *	1994-12-09	2000-01-15	만셀 케이쓰 로드니	윤활유 및 첨가제 조합물을 포함하는 윤활유 조성물, 첨가제 조합물을 함유하는 농축물 및 첨가제 조합물을 이용하여 윤활유 조성물의 산화방지 특성을 개선시키는 방법
US6569818B2 (en) *	2000-06-02	2003-05-27	Chevron Oronite Company, Llc	Lubricating oil composition
KR20020001594A (ko) *	2000-06-26	2002-01-09	가마이 고로	도광판, 면광원 장치 및 반사형 액정 표시 장치
US6777378B2 (en) *	2002-02-15	2004-08-17	The Lubrizol Corporation	Molybdenum, sulfur and boron containing lubricating oil composition

2007
- 2007-03-23 TW TW096110093A patent/TW200801174A/zh unknown
- 2007-03-28 US US12/294,441 patent/US20100286004A1/en not_active Abandoned
- 2007-03-28 WO PCT/US2007/065371 patent/WO2007115042A2/fr not_active Ceased
- 2007-03-28 AU AU2007233234A patent/AU2007233234A1/en not_active Abandoned
- 2007-03-28 JP JP2009503250A patent/JP2009531533A/ja not_active Withdrawn
- 2007-03-28 EA EA200870386A patent/EA200870386A1/ru unknown
- 2007-03-28 KR KR1020087023865A patent/KR20080103588A/ko not_active Withdrawn
- 2007-03-28 EP EP07759584A patent/EP2004780A2/fr not_active Withdrawn
- 2007-03-28 CA CA002647574A patent/CA2647574A1/fr not_active Abandoned
- 2007-03-28 CN CNA2007800116504A patent/CN101415805A/zh active Pending
- 2007-03-28 BR BRPI0710256-9A patent/BRPI0710256A2/pt not_active IP Right Cessation

Also Published As

Publication number	Publication date
EA200870386A1 (ru)	2009-04-28
JP2009531533A (ja)	2009-09-03
CN101415805A (zh)	2009-04-22
KR20080103588A (ko)	2008-11-27
WO2007115042A3 (fr)	2008-01-24
AU2007233234A1 (en)	2007-10-11
TW200801174A (en)	2008-01-01
EP2004780A2 (fr)	2008-12-24
US20100286004A1 (en)	2010-11-11
CA2647574A1 (fr)	2007-10-11
WO2007115042A2 (fr)	2007-10-11

Legal Events

Date	Code	Title	Description
2012-06-05	B08F	Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]	Free format text: REFERENTE AS 4A E 5A ANUIDADES.
2013-07-02	B08K	Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]	Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2161 DE 05/06/2012.

Publication	Publication Date	Title
BRPI0710256A2 (pt)	2011-08-09	composição de óleo lubrificante; composição concentrada de aditivo de óleo lubrificante, composição de óleo de motor; composição concentrada de aditivo de óleo de motor; e método de aumentar a concetração de pelo menos um antioxidante fenólico impedido em uma composição concentrada de aditivo de óleo lubrificante
US7928045B2 (en)	2011-04-19	Stabilizing compositions for lubricants
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JP2010522136A5 (fr)	2010-08-12
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WO2009076082A1 (fr)	2009-06-18	Compositions d'additif avec des produits d'addition de michael de phénylènediamines n-substituées
EP3310885B1 (fr)	2023-02-22	Composés contenant du molybdène multifonctionnels, procédé de fabrication et d'utilisation, et compositions d'huile lubrifiante contenant ceux-ci
JP2009523862A (ja)	2009-06-25	潤滑油および潤滑油添加剤濃厚液組成物
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