KR20230131234A - 색 안정성이 향상된 기유의 제조 방법 - Google Patents
색 안정성이 향상된 기유의 제조 방법 Download PDFInfo
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- KR20230131234A KR20230131234A KR1020237026537A KR20237026537A KR20230131234A KR 20230131234 A KR20230131234 A KR 20230131234A KR 1020237026537 A KR1020237026537 A KR 1020237026537A KR 20237026537 A KR20237026537 A KR 20237026537A KR 20230131234 A KR20230131234 A KR 20230131234A
- Authority
- KR
- South Korea
- Prior art keywords
- benzotriazol
- base oil
- color
- tert
- propyl
- Prior art date
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- 239000002199 base oil Substances 0.000 title claims abstract description 117
- 238000004519 manufacturing process Methods 0.000 title abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 77
- 239000000203 mixture Substances 0.000 claims abstract description 55
- -1 phenyl benzotriazole compound Chemical class 0.000 claims abstract description 50
- 125000001424 substituent group Chemical group 0.000 claims abstract description 22
- 239000001257 hydrogen Substances 0.000 claims abstract description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 5
- 230000008859 change Effects 0.000 claims description 24
- 230000005855 radiation Effects 0.000 claims description 17
- 230000006872 improvement Effects 0.000 claims description 9
- VQMHSKWEJGIXGA-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-dodecyl-4-methylphenol Chemical compound CCCCCCCCCCCCC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O VQMHSKWEJGIXGA-UHFFFAOYSA-N 0.000 claims description 4
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 3
- SFWASAKWKKYVLV-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-di(undecyl)phenol Chemical compound CCCCCCCCCCCC(C=C1CCCCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O SFWASAKWKKYVLV-UHFFFAOYSA-N 0.000 claims description 3
- VEGSYRFCASRSCP-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-didecylphenol Chemical compound CCCCCCCCCCC(C=C1CCCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O VEGSYRFCASRSCP-UHFFFAOYSA-N 0.000 claims description 3
- SOLOXORWSAOQRU-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-butyl-6-decylphenol Chemical compound CCCCCCCCCCC1=CC(CCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O SOLOXORWSAOQRU-UHFFFAOYSA-N 0.000 claims description 3
- OJPAVEGDGQWZLQ-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-butyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(CCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O OJPAVEGDGQWZLQ-UHFFFAOYSA-N 0.000 claims description 3
- WHTYMWHOOMDUCQ-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-butylphenol Chemical compound CCCCC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 WHTYMWHOOMDUCQ-UHFFFAOYSA-N 0.000 claims description 3
- XQASVDHNGHUGRM-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-decyl-6-nonylphenol Chemical compound CCCCCCCCCCC(C=C1CCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O XQASVDHNGHUGRM-UHFFFAOYSA-N 0.000 claims description 3
- NKCHIXVVFPCSTB-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-decylphenol Chemical compound CCCCCCCCCCC(C=C1)=CC(N2N=C(C=CC=C3)C3=N2)=C1O NKCHIXVVFPCSTB-UHFFFAOYSA-N 0.000 claims description 3
- ODHAEXHMQLBIMN-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-dodecyl-6-nonylphenol Chemical compound CCCCCCCCCCCCC(C=C1CCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O ODHAEXHMQLBIMN-UHFFFAOYSA-N 0.000 claims description 3
- RKVRWKDTXOIXNG-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 RKVRWKDTXOIXNG-UHFFFAOYSA-N 0.000 claims description 3
- NUMXKKYSPKYWKI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-ethyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(CC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O NUMXKKYSPKYWKI-UHFFFAOYSA-N 0.000 claims description 3
- UIOQCCACVKRIHO-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-ethyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O UIOQCCACVKRIHO-UHFFFAOYSA-N 0.000 claims description 3
- NAHKJPXTQGGPSZ-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-ethylphenol Chemical compound CCC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 NAHKJPXTQGGPSZ-UHFFFAOYSA-N 0.000 claims description 3
- IKSBZSSLSAADNS-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-heptyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(CCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O IKSBZSSLSAADNS-UHFFFAOYSA-N 0.000 claims description 3
- LJYWYBXXUOGVNT-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-heptyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O LJYWYBXXUOGVNT-UHFFFAOYSA-N 0.000 claims description 3
- PZOAHMAPQXBXNR-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-heptylphenol Chemical compound OC1=C(C=C(C=C1)CCCCCCC)N1N=C2C(=N1)C=CC=C2 PZOAHMAPQXBXNR-UHFFFAOYSA-N 0.000 claims description 3
- ZHWUZCLPSLHKIL-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-hexyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(CCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O ZHWUZCLPSLHKIL-UHFFFAOYSA-N 0.000 claims description 3
- VBQVHUUKCOKAGC-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-methyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(C)=CC(N2N=C(C=CC=C3)C3=N2)=C1O VBQVHUUKCOKAGC-UHFFFAOYSA-N 0.000 claims description 3
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- QEQYURHGSJOCPM-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-nonyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O QEQYURHGSJOCPM-UHFFFAOYSA-N 0.000 claims description 3
- MYYBPUHIKGRHEA-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MYYBPUHIKGRHEA-UHFFFAOYSA-N 0.000 claims description 3
- ODMAISQBTXJPQV-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-octyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O ODMAISQBTXJPQV-UHFFFAOYSA-N 0.000 claims description 3
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- KZMSNSYZULEKPH-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-pentyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O KZMSNSYZULEKPH-UHFFFAOYSA-N 0.000 claims description 3
- SYFIBOFYDHBYCD-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-pentylphenol Chemical compound CCCCCC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 SYFIBOFYDHBYCD-UHFFFAOYSA-N 0.000 claims description 3
- LLCXJCRXHADJRI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-propyl-6-undecylphenol Chemical compound CCCCCCCCCCCC1=CC(CCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O LLCXJCRXHADJRI-UHFFFAOYSA-N 0.000 claims description 3
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- XCRKICZTDSIDHI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-decyl-4-dodecylphenol Chemical compound CCCCCCCCCCCCC(C=C1CCCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O XCRKICZTDSIDHI-UHFFFAOYSA-N 0.000 claims description 3
- IVQVGWBMEFDCDC-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-decyl-4-ethylphenol Chemical compound CCCCCCCCCCC1=CC(CC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O IVQVGWBMEFDCDC-UHFFFAOYSA-N 0.000 claims description 3
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- 238000005259 measurement Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- BQFBKBCRVDJBKV-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4-dodecyl-6-undecylphenol Chemical compound CCCCCCCCCCCCC(C=C1CCCCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O BQFBKBCRVDJBKV-UHFFFAOYSA-N 0.000 description 1
- BVMWMIJQLRZGAM-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-decyl-4-undecylphenol Chemical compound CCCCCCCCCCCC(C=C1CCCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O BVMWMIJQLRZGAM-UHFFFAOYSA-N 0.000 description 1
- AZMMOXQMWSFKBK-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-nonyl-4-undecylphenol Chemical compound CCCCCCCCCCCC(C=C1CCCCCCCCC)=CC(N2N=C(C=CC=C3)C3=N2)=C1O AZMMOXQMWSFKBK-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052800 carbon group element Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 229910021476 group 6 element Inorganic materials 0.000 description 1
- 229910021474 group 7 element Inorganic materials 0.000 description 1
- 229910021472 group 8 element Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 230000028161 membrane depolarization Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 125000001741 organic sulfur group Chemical group 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000013077 target material Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/12—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
- C10M133/14—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
-
- 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
-
- 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
- C10M2203/003—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions 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
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen 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
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/223—Five-membered rings containing nitrogen and carbon only
-
- 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
- C10N2020/02—Viscosity; Viscosity index
-
- 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
- C10N2030/32—Light or X-ray resistance
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 (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US202163138796P | 2021-01-19 | 2021-01-19 | |
| US63/138,796 | 2021-01-19 | ||
| US202117154099A | 2021-01-21 | 2021-01-21 | |
| US17/154,099 | 2021-01-21 | ||
| PCT/US2022/012698 WO2022159358A1 (en) | 2021-01-19 | 2022-01-18 | Method for making base oil with enhanced color stability |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20230131234A true KR20230131234A (ko) | 2023-09-12 |
Family
ID=80225383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020237026537A KR20230131234A (ko) | 2021-01-19 | 2022-01-18 | 색 안정성이 향상된 기유의 제조 방법 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20240110120A1 (pt) |
| EP (1) | EP4281528A1 (pt) |
| JP (1) | JP2024503483A (pt) |
| KR (1) | KR20230131234A (pt) |
| BR (1) | BR112023014393A2 (pt) |
| CA (1) | CA3208347A1 (pt) |
| TW (1) | TW202246475A (pt) |
| WO (1) | WO2022159358A1 (pt) |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3282842A (en) * | 1964-03-06 | 1966-11-01 | Mobil Oil Corp | Lubricating oil compositions |
| US3518193A (en) * | 1964-05-12 | 1970-06-30 | Universal Oil Prod Co | Synergistic antioxidant mixture and use thereof |
| US3852207A (en) | 1973-03-26 | 1974-12-03 | Chevron Res | Production of stable lubricating oils by sequential hydrocracking and hydrogenation |
| US4673487A (en) | 1984-11-13 | 1987-06-16 | Chevron Research Company | Hydrogenation of a hydrocrackate using a hydrofinishing catalyst comprising palladium |
| TW327185B (en) * | 1993-09-20 | 1998-02-21 | Ciba Sc Holding Ag | Liquid antioxidants |
| JP4634585B2 (ja) * | 2000-08-10 | 2011-02-16 | 昭和シェル石油株式会社 | 防錆性および耐摩耗性が改良されたグリース組成物 |
| US6468501B1 (en) | 2000-09-14 | 2002-10-22 | Chevrontexaco Corporation | Method for heteroatom lattice substitution in large and extra-large pore borosilicate zeolites |
| US9487723B2 (en) * | 2010-06-29 | 2016-11-08 | Exxonmobil Research And Engineering Company | High viscosity high quality group II lube base stocks |
| JP6165672B2 (ja) * | 2014-05-14 | 2017-07-19 | Ｊｘｔｇエネルギー株式会社 | 潤滑油組成物及び製造ラインの管理方法 |
| KR102434564B1 (ko) * | 2016-08-31 | 2022-08-19 | 이데미쓰 고산 가부시키가이샤 | 진공 펌프유 |
| CN106590875A (zh) * | 2016-12-03 | 2017-04-26 | 马光德 | 一种具有优异散热性能的纳米改性变压器油及其制备方法 |
-
2022
- 2022-01-18 CA CA3208347A patent/CA3208347A1/en active Pending
- 2022-01-18 EP EP22702585.5A patent/EP4281528A1/en active Pending
- 2022-01-18 BR BR112023014393A patent/BR112023014393A2/pt unknown
- 2022-01-18 KR KR1020237026537A patent/KR20230131234A/ko unknown
- 2022-01-18 JP JP2023543165A patent/JP2024503483A/ja active Pending
- 2022-01-18 WO PCT/US2022/012698 patent/WO2022159358A1/en active Application Filing
- 2022-01-18 US US18/262,171 patent/US20240110120A1/en active Pending
- 2022-01-19 TW TW111102266A patent/TW202246475A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20240110120A1 (en) | 2024-04-04 |
| WO2022159358A1 (en) | 2022-07-28 |
| CA3208347A1 (en) | 2022-07-28 |
| TW202246475A (zh) | 2022-12-01 |
| EP4281528A1 (en) | 2023-11-29 |
| JP2024503483A (ja) | 2024-01-25 |
| BR112023014393A2 (pt) | 2023-09-26 |
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