SG187200A1 - Application-specific finished lubricant compositions comprising a bio-derived ester component and methods of making same - Google Patents
Application-specific finished lubricant compositions comprising a bio-derived ester component and methods of making same Download PDFInfo
- Publication number
- SG187200A1 SG187200A1 SG2013006069A SG2013006069A SG187200A1 SG 187200 A1 SG187200 A1 SG 187200A1 SG 2013006069 A SG2013006069 A SG 2013006069A SG 2013006069 A SG2013006069 A SG 2013006069A SG 187200 A1 SG187200 A1 SG 187200A1
- Authority
- SG
- Singapore
- Prior art keywords
- isomers
- acid
- ester
- oils
- agents
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 80
- 239000000314 lubricant Substances 0.000 title claims abstract description 66
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 150000002148 esters Chemical class 0.000 title claims description 26
- 150000005690 diesters Chemical class 0.000 claims abstract description 65
- 239000000654 additive Substances 0.000 claims abstract description 31
- 239000002199 base oil Substances 0.000 claims abstract description 30
- 230000000996 additive effect Effects 0.000 claims abstract description 21
- 239000002028 Biomass Substances 0.000 claims abstract description 15
- 230000008569 process Effects 0.000 claims description 56
- 150000001336 alkenes Chemical class 0.000 claims description 31
- 239000003921 oil Substances 0.000 claims description 31
- 239000012374 esterification agent Substances 0.000 claims description 23
- 239000012530 fluid Substances 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 19
- 150000004665 fatty acids Chemical group 0.000 claims description 17
- -1 acyl anhydrides Chemical class 0.000 claims description 16
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 14
- 239000003112 inhibitor Substances 0.000 claims description 14
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 12
- 239000010725 compressor oil Substances 0.000 claims description 9
- 238000005555 metalworking Methods 0.000 claims description 9
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
- 239000010723 turbine oil Substances 0.000 claims description 9
- 239000003963 antioxidant agent Substances 0.000 claims description 8
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 claims description 8
- 239000003377 acid catalyst Substances 0.000 claims description 7
- 150000001735 carboxylic acids Chemical class 0.000 claims description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 7
- 239000006078 metal deactivator Substances 0.000 claims description 7
- 150000003626 triacylglycerols Chemical class 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 6
- 238000000926 separation method Methods 0.000 claims description 6
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000010705 motor oil Substances 0.000 claims description 5
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002841 Lewis acid Substances 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 238000005260 corrosion Methods 0.000 claims description 4
- 230000007797 corrosion Effects 0.000 claims description 4
- 238000009795 derivation Methods 0.000 claims description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 150000007517 lewis acids Chemical class 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims description 4
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 claims description 3
- DUSDZNHXSASWEZ-UHFFFAOYSA-N 5-decanoyloxyoctan-4-yl decanoate Chemical compound CCCCCCCCCC(=O)OC(CCC)C(CCC)OC(=O)CCCCCCCCC DUSDZNHXSASWEZ-UHFFFAOYSA-N 0.000 claims description 3
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 3
- 150000001266 acyl halides Chemical class 0.000 claims description 3
- 239000002518 antifoaming agent Substances 0.000 claims description 3
- 239000008139 complexing agent Substances 0.000 claims description 3
- 239000003599 detergent Substances 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 239000010721 machine oil Substances 0.000 claims description 3
- 239000003607 modifier Substances 0.000 claims description 3
- 239000011973 solid acid Substances 0.000 claims description 3
- RPSBNRRYNLCCNR-UHFFFAOYSA-N 6-decanoyloxydecan-5-yl decanoate Chemical compound CCCCCCCCCC(=O)OC(CCCC)C(CCCC)OC(=O)CCCCCCCCC RPSBNRRYNLCCNR-UHFFFAOYSA-N 0.000 claims description 2
- SSDCEMRVDZSXAM-UHFFFAOYSA-N 7-dodecanoyloxydodecan-6-yl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC(CCCCC)C(CCCCC)OC(=O)CCCCCCCCCCC SSDCEMRVDZSXAM-UHFFFAOYSA-N 0.000 claims description 2
- NXIJJWHBQDQCMB-UHFFFAOYSA-N 8-octanoyloxytetradecan-7-yl octanoate Chemical compound CCCCCCCC(=O)OC(CCCCCC)C(CCCCCC)OC(=O)CCCCCCC NXIJJWHBQDQCMB-UHFFFAOYSA-N 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 229920001429 chelating resin Polymers 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 238000006317 isomerization reaction Methods 0.000 claims description 2
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims description 2
- 229910001930 tungsten oxide Inorganic materials 0.000 claims description 2
- AYZWOWZRWSEQNZ-UHFFFAOYSA-N 5-tetradecanoyloxyoctan-4-yl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(CCC)C(CCC)OC(=O)CCCCCCCCCCCCC AYZWOWZRWSEQNZ-UHFFFAOYSA-N 0.000 claims 1
- HRAWAJPQVRFKNQ-UHFFFAOYSA-N 6-octanoyloxydecan-5-yl octanoate Chemical compound CCCCCCCC(=O)OC(CCCC)C(CCCC)OC(=O)CCCCCCC HRAWAJPQVRFKNQ-UHFFFAOYSA-N 0.000 claims 1
- FDSPXIQONIJWJC-UHFFFAOYSA-N 7-hexanoyloxydodecan-6-yl hexanoate Chemical compound CCCCCC(=O)OC(CCCCC)C(CCCCC)OC(=O)CCCCC FDSPXIQONIJWJC-UHFFFAOYSA-N 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- 239000000047 product Substances 0.000 abstract description 9
- 239000006227 byproduct Substances 0.000 abstract description 6
- 239000007795 chemical reaction product Substances 0.000 abstract description 4
- 239000007788 liquid Substances 0.000 abstract description 3
- 239000004711 α-olefin Substances 0.000 abstract description 2
- 125000005313 fatty acid group Chemical group 0.000 abstract 1
- 241000894007 species Species 0.000 description 46
- 235000019198 oils Nutrition 0.000 description 27
- 230000015572 biosynthetic process Effects 0.000 description 10
- 150000002118 epoxides Chemical group 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 150000002009 diols Chemical class 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- 230000032050 esterification Effects 0.000 description 7
- 238000005886 esterification reaction Methods 0.000 description 7
- 238000003786 synthesis reaction Methods 0.000 description 7
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 6
- 238000006735 epoxidation reaction Methods 0.000 description 6
- 239000012634 fragment Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 230000037361 pathway Effects 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 229920013639 polyalphaolefin Polymers 0.000 description 4
- 150000004671 saturated fatty acids Chemical class 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000001640 fractional crystallisation Methods 0.000 description 3
- 239000010720 hydraulic oil Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 235000003441 saturated fatty acids Nutrition 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000005069 Extreme pressure additive Substances 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 239000007866 anti-wear additive Substances 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000003879 lubricant additive Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000007142 ring opening reaction Methods 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
- SMZRETBRUDBXEL-UHFFFAOYSA-N 5-dodecanoyloxyoctan-4-yl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC(CCC)C(CCC)OC(=O)CCCCCCCCCCC SMZRETBRUDBXEL-UHFFFAOYSA-N 0.000 description 1
- AOPPCVBFJDZSMU-UHFFFAOYSA-N 5-hexanoyloxyoctan-4-yl hexanoate Chemical compound CCCCCC(=O)OC(CCC)C(CCC)OC(=O)CCCCC AOPPCVBFJDZSMU-UHFFFAOYSA-N 0.000 description 1
- CUAULHCGVXJOOT-UHFFFAOYSA-N 6-tetradecanoyloxydecan-5-yl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(CCCC)C(CCCC)OC(=O)CCCCCCCCCCCCC CUAULHCGVXJOOT-UHFFFAOYSA-N 0.000 description 1
- AAETUAZYHYNUQH-UHFFFAOYSA-N 7-decanoyloxydodecan-6-yl decanoate Chemical compound CCCCCCCCCC(=O)OC(CCCCC)C(CCCCC)OC(=O)CCCCCCCCC AAETUAZYHYNUQH-UHFFFAOYSA-N 0.000 description 1
- WZPVFPWYSOLFTC-UHFFFAOYSA-N 7-octanoyloxydodecan-6-yl octanoate Chemical compound CCCCCCCC(=O)OC(CCCCC)C(CCCCC)OC(=O)CCCCCCC WZPVFPWYSOLFTC-UHFFFAOYSA-N 0.000 description 1
- VOQUJAKTXDMJCG-UHFFFAOYSA-N 8-decanoyloxytetradecan-7-yl decanoate Chemical compound CCCCCCCCCC(=O)OC(CCCCCC)C(CCCCCC)OC(=O)CCCCCCCCC VOQUJAKTXDMJCG-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 235000003332 Ilex aquifolium Nutrition 0.000 description 1
- 241000209027 Ilex aquifolium Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000283986 Lepus Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 239000002551 biofuel Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 235000019161 pantothenic acid Nutrition 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/74—Esters of polyhydroxy 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
- C10M2203/10—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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/2805—Esters 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
- 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
-
- 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
- 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
- C10N2030/08—Resistance to extreme temperature
-
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/70—Soluble oils
-
- 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
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
-
- 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
- C10N2040/135—Steam engines or turbines
-
- 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
- C10N2040/20—Metal working
-
- 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
- C10N2040/30—Refrigerators lubricants or compressors lubricants
-
- 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
- C10N2040/38—Conveyors or chain belts
-
- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/846,010 US20120028863A1 (en) | 2010-07-29 | 2010-07-29 | Application-specific finished lubricant compositions comprising a bio-derived ester component and methods of making same |
| PCT/US2011/045389 WO2012015824A2 (en) | 2010-07-29 | 2011-07-26 | Application-specific finished lubricant compositions comprising a bio-derived ester component and methods of making same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG187200A1 true SG187200A1 (en) | 2013-02-28 |
Family
ID=45527316
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG2013006069A SG187200A1 (en) | 2010-07-29 | 2011-07-26 | Application-specific finished lubricant compositions comprising a bio-derived ester component and methods of making same |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20120028863A1 (es) |
| CN (1) | CN103003398A (es) |
| BR (1) | BR112012031148A2 (es) |
| CA (1) | CA2801782A1 (es) |
| DE (1) | DE112011102541T5 (es) |
| MX (1) | MX2013000648A (es) |
| SG (1) | SG187200A1 (es) |
| WO (1) | WO2012015824A2 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103666705B (zh) * | 2013-12-14 | 2015-02-18 | 广西大学 | 一种蓖麻基防锈无渍液压液 |
| EP3124579A1 (en) * | 2015-07-31 | 2017-02-01 | Total Marketing Services | Lubricant composition comprising branched diesters and viscosity index improver |
| CN114507554B (zh) * | 2020-10-28 | 2023-04-11 | 中国石油化工股份有限公司 | 一种液压油组合物 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2537283A (en) | 1948-09-29 | 1951-01-09 | Universal Oil Prod Co | Isomerization of olefins |
| US3211801A (en) | 1961-12-08 | 1965-10-12 | Phillips Petroleum Co | Supported olefin conversion catalysts |
| GB1069044A (en) | 1963-05-02 | 1967-05-17 | Kurashiki Rayon Kk | Process for transferring double bond of olefin |
| US3270085A (en) | 1964-01-06 | 1966-08-30 | Dow Chemical Co | Method for isomerizing alpha olefins to beta olefins with chromium nickel phosphate |
| US3327014A (en) | 1964-01-06 | 1967-06-20 | Dow Chemical Co | Method for isomerizing alpha olefins to beta olefins with nickel-chromium phosphate |
| US3448164A (en) | 1967-09-21 | 1969-06-03 | Phillips Petroleum Co | Olefin skeletal isomerization and catalyst |
| BE757437A (fr) | 1969-11-24 | 1971-04-13 | Petro Tex Chem Corp | Procede d'isomerisation du butene-1 en cis-butene-2 |
| US4593146A (en) | 1985-03-29 | 1986-06-03 | Phillips Petroleum Company | Isomerization process and catalyst therefor |
| DE69727395T2 (de) | 1996-11-13 | 2004-11-04 | Chevron Phillips Chemical Company Lp, San Ramon | Verfahren zur olefinisomerisierung |
| US6165952A (en) * | 1999-04-05 | 2000-12-26 | King Industries, Inc. | Ashless rust inhibitor lubricant compositions |
| US7674364B2 (en) * | 2005-03-11 | 2010-03-09 | Chevron U.S.A. Inc. | Hydraulic fluid compositions and preparation thereof |
| JP4938250B2 (ja) * | 2005-04-28 | 2012-05-23 | 出光興産株式会社 | 動力伝達用潤滑剤 |
| US7871967B2 (en) * | 2007-02-12 | 2011-01-18 | Chevron U.S.A. Inc. | Diester-based lubricants and methods of making same |
| US8124572B2 (en) * | 2007-09-27 | 2012-02-28 | Chevron U.S.A. Inc. | Production of biofuels and biolubricants from a common feedstock |
| US7867959B2 (en) * | 2008-01-31 | 2011-01-11 | Chevron U.S.A. Inc. | Synthesis of diester-based biolubricants from epoxides |
| US9109238B2 (en) * | 2008-11-13 | 2015-08-18 | Chevron U.S.A. Inc. | Synthesis of diester-based lubricants from enzymatically-directed epoxides |
-
2010
- 2010-07-29 US US12/846,010 patent/US20120028863A1/en not_active Abandoned
-
2011
- 2011-07-26 CN CN2011800349534A patent/CN103003398A/zh active Pending
- 2011-07-26 CA CA2801782A patent/CA2801782A1/en not_active Abandoned
- 2011-07-26 SG SG2013006069A patent/SG187200A1/en unknown
- 2011-07-26 DE DE112011102541T patent/DE112011102541T5/de not_active Withdrawn
- 2011-07-26 BR BR112012031148A patent/BR112012031148A2/pt not_active IP Right Cessation
- 2011-07-26 WO PCT/US2011/045389 patent/WO2012015824A2/en active Application Filing
- 2011-07-26 MX MX2013000648A patent/MX2013000648A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20120028863A1 (en) | 2012-02-02 |
| CN103003398A (zh) | 2013-03-27 |
| DE112011102541T5 (de) | 2013-05-02 |
| CA2801782A1 (en) | 2012-02-02 |
| BR112012031148A2 (pt) | 2016-11-01 |
| WO2012015824A2 (en) | 2012-02-02 |
| WO2012015824A3 (en) | 2012-04-19 |
| MX2013000648A (es) | 2013-03-22 |
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