EP0279090B1 - Compositions d'essence contenant du molybdène hexavalent - Google Patents
Compositions d'essence contenant du molybdène hexavalent Download PDFInfo
- Publication number
- EP0279090B1 EP0279090B1 EP87301344A EP87301344A EP0279090B1 EP 0279090 B1 EP0279090 B1 EP 0279090B1 EP 87301344 A EP87301344 A EP 87301344A EP 87301344 A EP87301344 A EP 87301344A EP 0279090 B1 EP0279090 B1 EP 0279090B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- molybdenum
- gasoline
- fuel composition
- compound
- octane requirement
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 title claims description 99
- 239000000203 mixture Substances 0.000 title claims description 80
- 229910052750 molybdenum Inorganic materials 0.000 title claims description 49
- 239000011733 molybdenum Substances 0.000 title claims description 48
- -1 molybdenum(VI) compound Chemical class 0.000 claims abstract description 101
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims abstract description 95
- 238000002485 combustion reaction Methods 0.000 claims abstract description 56
- 239000000446 fuel Substances 0.000 claims description 93
- 229930195733 hydrocarbon Natural products 0.000 claims description 51
- 150000002430 hydrocarbons Chemical class 0.000 claims description 51
- 239000004215 Carbon black (E152) Substances 0.000 claims description 47
- 239000007788 liquid Substances 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 14
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 238000009835 boiling Methods 0.000 claims description 11
- 150000002739 metals Chemical class 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 239000011574 phosphorus Substances 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000005608 naphthenic acid group Chemical class 0.000 claims description 6
- 150000004985 diamines Chemical class 0.000 claims description 5
- 239000003446 ligand Substances 0.000 claims description 5
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 22
- 239000005078 molybdenum compound Substances 0.000 description 22
- 150000002752 molybdenum compounds Chemical class 0.000 description 22
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 15
- 239000006079 antiknock agent Substances 0.000 description 13
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical class O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000000654 additive Substances 0.000 description 10
- 239000010687 lubricating oil Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 238000010348 incorporation Methods 0.000 description 9
- 238000010992 reflux Methods 0.000 description 9
- 125000001183 hydrocarbyl group Chemical group 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 230000003647 oxidation Effects 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 239000003208 petroleum Substances 0.000 description 7
- 150000002989 phenols Chemical class 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- QXYJCZRRLLQGCR-UHFFFAOYSA-N dioxomolybdenum Chemical compound O=[Mo]=O QXYJCZRRLLQGCR-UHFFFAOYSA-N 0.000 description 6
- 150000002611 lead compounds Chemical class 0.000 description 6
- 239000000314 lubricant Substances 0.000 description 6
- 230000001629 suppression Effects 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 150000002751 molybdenum Chemical class 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- YRAJNWYBUCUFBD-UHFFFAOYSA-N 2,2,6,6-tetramethylheptane-3,5-dione Chemical compound CC(C)(C)C(=O)CC(=O)C(C)(C)C YRAJNWYBUCUFBD-UHFFFAOYSA-N 0.000 description 4
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 150000003460 sulfonic acids Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 230000029936 alkylation Effects 0.000 description 3
- 238000005804 alkylation reaction Methods 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000002199 base oil Substances 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000003254 gasoline additive Substances 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 230000001050 lubricating effect Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 150000002902 organometallic compounds Chemical class 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 150000002697 manganese compounds Chemical class 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 125000005474 octanoate group Chemical group 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical class CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- DDHUNHGZUHZNKB-UHFFFAOYSA-N 2,2-dimethylpropane-1,3-diamine Chemical compound NCC(C)(C)CN DDHUNHGZUHZNKB-UHFFFAOYSA-N 0.000 description 1
- JKTAIYGNOFSMCE-UHFFFAOYSA-N 2,3-di(nonyl)phenol Chemical class CCCCCCCCCC1=CC=CC(O)=C1CCCCCCCCC JKTAIYGNOFSMCE-UHFFFAOYSA-N 0.000 description 1
- BPRYUXCVCCNUFE-UHFFFAOYSA-N 2,4,6-trimethylphenol Chemical compound CC1=CC(C)=C(O)C(C)=C1 BPRYUXCVCCNUFE-UHFFFAOYSA-N 0.000 description 1
- SBMPIZWDWDNTJU-UHFFFAOYSA-N 2,4-didodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C(CCCCCCCCCCCC)=C1 SBMPIZWDWDNTJU-UHFFFAOYSA-N 0.000 description 1
- CEGGECULKVTYMM-UHFFFAOYSA-N 2,6-dimethylheptane-3,5-dione Chemical compound CC(C)C(=O)CC(=O)C(C)C CEGGECULKVTYMM-UHFFFAOYSA-N 0.000 description 1
- GJMUCDMIIVSROW-UHFFFAOYSA-N 2,8-dimethylnonane-4,6-dione Chemical compound CC(C)CC(=O)CC(=O)CC(C)C GJMUCDMIIVSROW-UHFFFAOYSA-N 0.000 description 1
- JUBNMICNBGWPRR-UHFFFAOYSA-J 2-(3-methylcyclopentyl)acetate molybdenum(4+) Chemical compound CC1CC(CC1)CC(=O)[O-].[Mo+4].CC1CC(CC1)CC(=O)[O-].CC1CC(CC1)CC(=O)[O-].CC1CC(CC1)CC(=O)[O-] JUBNMICNBGWPRR-UHFFFAOYSA-J 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- KZELEKCSKLUYAS-UHFFFAOYSA-J 2-cyclopentylacetate molybdenum(4+) Chemical compound C1(CCCC1)CC(=O)[O-].[Mo+4].C1(CCCC1)CC(=O)[O-].C1(CCCC1)CC(=O)[O-].C1(CCCC1)CC(=O)[O-] KZELEKCSKLUYAS-UHFFFAOYSA-J 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- YKJSOAKPHMIDLP-UHFFFAOYSA-J 2-ethylhexanoate;molybdenum(4+) Chemical compound [Mo+4].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O YKJSOAKPHMIDLP-UHFFFAOYSA-J 0.000 description 1
- BDXGMDGYOIWKIF-UHFFFAOYSA-N 2-methylpropane-1,3-diamine Chemical compound NCC(C)CN BDXGMDGYOIWKIF-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
- JZBVVNOPMZSANQ-UHFFFAOYSA-N 3,3-dimethylbutan-2-one Chemical compound CC(=O)C(C)(C)C.CC(=O)C(C)(C)C JZBVVNOPMZSANQ-UHFFFAOYSA-N 0.000 description 1
- UUMLGOUCUSYIAU-UHFFFAOYSA-N 3-dodecyl-6-hydroxycyclohexa-2,4-dien-1-one Chemical compound O=C1C(C=CC(=C1)CCCCCCCCCCCC)O UUMLGOUCUSYIAU-UHFFFAOYSA-N 0.000 description 1
- VTEUOJYHOLBKID-UHFFFAOYSA-J 3-dodecylcyclohexane-1-carboxylate molybdenum(4+) Chemical compound C(CCCCCCCCCCC)C1CC(CCC1)C(=O)[O-].[Mo+4].C(CCCCCCCCCCC)C1CC(CCC1)C(=O)[O-].C(CCCCCCCCCCC)C1CC(CCC1)C(=O)[O-].C(CCCCCCCCCCC)C1CC(CCC1)C(=O)[O-] VTEUOJYHOLBKID-UHFFFAOYSA-J 0.000 description 1
- GSOHKPVFCOWKPU-UHFFFAOYSA-N 3-methylpentane-2,4-dione Chemical compound CC(=O)C(C)C(C)=O GSOHKPVFCOWKPU-UHFFFAOYSA-N 0.000 description 1
- BPIHCIRSGQKCLT-UHFFFAOYSA-N 3-propan-2-ylpentane-2,4-dione Chemical compound CC(C)C(C(C)=O)C(C)=O BPIHCIRSGQKCLT-UHFFFAOYSA-N 0.000 description 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical class C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- OKUMHINSMZOUIZ-UHFFFAOYSA-N 4-(2-ethylhexyl)phenol Chemical compound CCCCC(CC)CC1=CC=C(O)C=C1 OKUMHINSMZOUIZ-UHFFFAOYSA-N 0.000 description 1
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 1
- FIJLPSJMPXGRJL-UHFFFAOYSA-N 4-Methylheptane-3,5-dione Chemical compound CCC(=O)C(C)C(=O)CC FIJLPSJMPXGRJL-UHFFFAOYSA-N 0.000 description 1
- NKXZDXDSOFEDSF-KTKRTIGZSA-N 4-[(z)-octadec-9-enyl]phenol Chemical compound CCCCCCCC\C=C/CCCCCCCCC1=CC=C(O)C=C1 NKXZDXDSOFEDSF-KTKRTIGZSA-N 0.000 description 1
- QIZUBPHXHVWGHD-UHFFFAOYSA-N 4-octadecylphenol Chemical compound CCCCCCCCCCCCCCCCCCC1=CC=C(O)C=C1 QIZUBPHXHVWGHD-UHFFFAOYSA-N 0.000 description 1
- KHZGUWAFFHXZLC-UHFFFAOYSA-N 5-methylhexane-2,4-dione Chemical compound CC(C)C(=O)CC(C)=O KHZGUWAFFHXZLC-UHFFFAOYSA-N 0.000 description 1
- IGMOYJSFRIASIE-UHFFFAOYSA-N 6-Methylheptan-2,4-dione Chemical compound CC(C)CC(=O)CC(C)=O IGMOYJSFRIASIE-UHFFFAOYSA-N 0.000 description 1
- PKAVSIHPPVFDHU-UHFFFAOYSA-N 7-methyloctane-3,5-dione Chemical compound CCC(=O)CC(=O)CC(C)C PKAVSIHPPVFDHU-UHFFFAOYSA-N 0.000 description 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- BLVIWFXPWAYTAB-UHFFFAOYSA-J C(CCCC)(=O)[O-].[Mo+4].C(CCCC)(=O)[O-].C(CCCC)(=O)[O-].C(CCCC)(=O)[O-] Chemical compound C(CCCC)(=O)[O-].[Mo+4].C(CCCC)(=O)[O-].C(CCCC)(=O)[O-].C(CCCC)(=O)[O-] BLVIWFXPWAYTAB-UHFFFAOYSA-J 0.000 description 1
- PYJBHIKDWKTOGU-UHFFFAOYSA-J C(CCCCCCCCCCC)(=O)[O-].[Mo+4].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] Chemical compound C(CCCCCCCCCCC)(=O)[O-].[Mo+4].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] PYJBHIKDWKTOGU-UHFFFAOYSA-J 0.000 description 1
- RURHXWFFEQJVTM-UHFFFAOYSA-J C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.[Mo+4].C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1 Chemical compound C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.[Mo+4].C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1.C(CCCCCCCCCCC)C1=CC=C(C(=O)[O-])C=C1 RURHXWFFEQJVTM-UHFFFAOYSA-J 0.000 description 1
- CLLMBHCKCCOJQC-UHFFFAOYSA-J C(CCCCCCCCCCCCC)(=O)[O-].[Mo+4].C(CCCCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCCCC)(=O)[O-] Chemical compound C(CCCCCCCCCCCCC)(=O)[O-].[Mo+4].C(CCCCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCCCC)(=O)[O-] CLLMBHCKCCOJQC-UHFFFAOYSA-J 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/1814—Chelates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1828—Salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
- C10L1/2431—Organic compounds containing sulfur, selenium and/or tellurium sulfur bond to oxygen, e.g. sulfones, sulfoxides
- C10L1/2437—Sulfonic acids; Derivatives thereof, e.g. sulfonamides, sulfosuccinic acid esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2633—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
Definitions
- One aspect of the invention is an unleaded gasoline, used in "clean,” new engines, containing a low concentration of a hydrocarbon soluble molybdenum (VI) compound comprising a major portion of gasoline and about 0.1 to about 20 parts of the molybdenum (VI) compound per one million parts of gasoline.
- a molybdenum (VI) compound can be used in an amount which is sufficient to provide from about 0.01 to about 10 parts of molybdenum, calculated as the metal, per million parts of gasoline.
- a further aspect of the invention is a concentrate of a hydrocarbon soluble molybdenum (VI) compound containing about 0.1 to about 50 wt% of the compound in a suitable diluent which can be dissolved in proper proportion in gasoline or lubricating oil to provide about 0.1 to about 10,000 parts of molybdenum (VI) compound per one million parts of gasoline or about 0.001 to about 5 wt% of molybdenbum (VI) compound in a lubricating oil.
- a hydrocarbon soluble molybdenum (VI) compound containing about 0.1 to about 50 wt% of the compound in a suitable diluent which can be dissolved in proper proportion in gasoline or lubricating oil to provide about 0.1 to about 10,000 parts of molybdenum (VI) compound per one million parts of gasoline or about 0.001 to about 5 wt% of molybdenbum (VI) compound in a lubricating oil.
- any hydrocarbon soluble molybdenum(VI) compound which is stable in hydrocarbon or petroleum storage or distribution facilities can be used in gasoline in accordance with this invention.
- the molybdenum(VI) or compound is selected from the group consisting of molybdenum(VI) sulfonates, molybdenum(VI) diamine complexes, amine salts of molybdic acid and isopoly molybdic acid, and molybdenum(VI) compounds which are free of nitrogen, sulfur and phosphorus.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
Claims (10)
- Composition de carburant à base d'essence, comprenant une proportion majeure d'un carburant hydrocarboné liquide du domaine d'ébullition de l'essence, en combinaison avec un composé de molybdène (VI) qui est soluble dans ledit carburant hydrocarboné, dans laquelle la quantité dudit composé de molybdène (VI) est suffisante pour fournir de 0,01 à 1000 parties de molybdène par million de parties de carburant hydrocarboné, ladite composition de carburant est essentiellement exempte de métaux autres que le molybdène, et ledit composé de molybdène (VI) est choisi parmi les sulfonates de molybdène (VI), les complexes de molybdène (VI)-diamine dans lesquels le ligand diamine a pour formule R⁴R⁵N-(CR⁴R⁵)n-NR⁴R⁵, dans laquelle n est un nombre entier de 1 à 20 et chaque R⁴ et R⁵ est choisi indépendamment parmi un hydrogène et un groupe alkyle de 1 à 20 atomes de carbone, et les composé de molybdène (VI) qui sont exempts d'azote, de soufre et de phosphore.
- Composition de carburant à base d'essence selon la revendication 1, dans laquelle ledit composé de molybdène (VI) est choisi parmi les carboxylates de molybdène (VI), les sels de molybdène (VI) d'acides naphténiques, les phénates de molybdène (VI), les alcoolates de molybdène (VI), les aryloxydes de molybdène (VI) et les composés molybdène (VI)-β-dicétone.
- Composition de carburant à base d'essence selon la revendication 1, dans laquelle ledit composé de molybdène (VI) est un complexe molybdène (VI)-β-dicétone.
- Composition de carburant à base d'essence selon l'une quelconque des revendications précédentes, qui comprend, en outre, une quantité mineure de méthyl-t-butyléther efficace pour réduire la détonation dans un moteur à combustion interne à allumage par étincelle.
- Composition de carburant à base d'essence selon l'une quelconque des revendications 1 à 4, dans laquelle la quantité dudit composé de molybdène (VI) est de 0,1 à 20,0 parties par million de parties du carburant hydrocarboné.
- Composition de carburant à base d'essence selon l'une quelconque des revendications 1 à 4, dans laquelle la quantité dudit composé de molybdène (VI) est suffisante pour fournir de 0,01 à 10 parties de molybdène par million de parties dudit carburant hydrocarboné.
- Composition de carburant à base d'essence selon l'une quelconque des revendications 1 à 4, dans laquelle la quantité dudit composé de molybdène (VI) est suffisante pour fournir de 10 à 1000 parties de molybdène par million de parties dudit carburant hydrocarboné.
- Procédé pour abaisser-élever le besoin en indice d'octane en régime permanent et/ou pour freiner la hausse du besoin en indice d'octane dans un moteur à combustion interne à allumage par étincelle, ce procédé comprenant le fonctionnement dudit moteur avec la composition de carburant à base d'essence selon l'une quelconque des revendications 1 à 7.
- Procédé selon la revendication 8 pour abaisser un besoin en indice d'octane élevée en régime permanent dans un moteur à combustion interne à allumage par étincelle et pour maintenir le besoin en indice d'octane réduit résultant en régime permanent, qui comprend les étapes qui consistent à faire fonctionner ledit moteur avec une première composition de carburant à base d'essence jusqu'à ce que l'on obtienne un besoin en indice d'octane réduit en régime permanent et à maintenir ledit besoin en indice d'octane réduit en régime permanent en faisant fonctionner le moteur avec une seconde composition de carburant à base d'essence, dans lequel ladite première composition de carburant comprend une composition de carburant à base d'essence selon la revendication 7 et dans lequel ladite seconde composition de carburant comprend une composition de carburant à base d'essence selon la revendication 6.
- Procédé selon la revendication 8 pour abaisser un besoin en indice d'octane élevé en régime permanent dans un moteur à combustion interne à allumage par étincelle ayant un besoin en indice d'octane accru d'environ 2 à environ 7 unités après un fonctionnement avec de l'essence essentiellement exempte de plomb et de molybdène, qui comprend le fonctionnement dudit moteur avec une composition de carburant à base d'essence selon la revendication 7 et la quantité de ladite composition de carburant à base d'essence est efficace pour abaisser ledit besoin en indice d'octane élevé en régime permanent d'au moins environ 20%.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/833,225 US4647293A (en) | 1980-09-25 | 1986-02-24 | Gasoline compositions containing hexavalent molybdenum |
AT87301344T ATE69835T1 (de) | 1987-02-17 | 1987-02-17 | Sechswertiges molybdaen enthaltende benzinzusammensetzungen. |
DE8787301344T DE3774868D1 (de) | 1987-02-17 | 1987-02-17 | Sechswertiges molybdaen enthaltende benzinzusammensetzungen. |
EP87301344A EP0279090B1 (fr) | 1987-02-17 | 1987-02-17 | Compositions d'essence contenant du molybdène hexavalent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP87301344A EP0279090B1 (fr) | 1987-02-17 | 1987-02-17 | Compositions d'essence contenant du molybdène hexavalent |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0279090A1 EP0279090A1 (fr) | 1988-08-24 |
EP0279090B1 true EP0279090B1 (fr) | 1991-11-27 |
Family
ID=8197792
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87301344A Expired EP0279090B1 (fr) | 1980-09-25 | 1987-02-17 | Compositions d'essence contenant du molybdène hexavalent |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0279090B1 (fr) |
AT (1) | ATE69835T1 (fr) |
DE (1) | DE3774868D1 (fr) |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3124600A (en) * | 1964-03-10 | Organometallic compounds | ||
US2086775A (en) * | 1936-07-13 | 1937-07-13 | Leo Corp | Method of operating an internal combustion engine |
GB770278A (en) * | 1954-04-30 | 1957-03-20 | Exxon Research Engineering Co | Fuel composition |
US2881062A (en) * | 1955-08-17 | 1959-04-07 | Tide Water Associated Oil Comp | Hydrocarbon fuel |
GB894852A (en) * | 1958-12-08 | 1962-04-26 | Geoffrey Wilkinson | Cycloheptatrienyl metallocarbonyl compounds |
US3168368A (en) * | 1960-04-27 | 1965-02-02 | Air Prod & Chem | Method of treating exhaust gases of internal combustion engines |
US3282838A (en) * | 1960-05-10 | 1966-11-01 | Texaco Inc | Petroleum liquids containing amine salts of molybdic acid |
US3093671A (en) * | 1960-11-14 | 1963-06-11 | Ethyl Corp | Cyclic diene group vi-beta metal carbonyls |
NL273044A (fr) * | 1960-12-30 | |||
US3755195A (en) * | 1968-12-20 | 1973-08-28 | Ethyl Corp | Spark plug anti-foulant |
AU5525773A (en) * | 1972-06-14 | 1974-11-07 | Continental Oil Co | Stable oil-soluble metal sulfonate compositions stable oil-soluble metal sulfonate compositions |
US4266945A (en) * | 1979-11-23 | 1981-05-12 | The Lubrizol Corporation | Molybdenum-containing compositions and lubricants and fuels containing them |
US4647293A (en) * | 1980-09-25 | 1987-03-03 | William H. Magidson | Gasoline compositions containing hexavalent molybdenum |
US4357149A (en) * | 1980-09-25 | 1982-11-02 | Standard Oil Company (Indiana) | Hydrocarbon-soluble oxidized, sulfurized polyamine-molbdenum compositions and gasoline containing same |
GB2089431B (en) * | 1980-12-06 | 1984-06-06 | Weir Pumps Ltd | Preventing surge in pumps |
-
1987
- 1987-02-17 AT AT87301344T patent/ATE69835T1/de not_active IP Right Cessation
- 1987-02-17 EP EP87301344A patent/EP0279090B1/fr not_active Expired
- 1987-02-17 DE DE8787301344T patent/DE3774868D1/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE3774868D1 (de) | 1992-01-09 |
EP0279090A1 (fr) | 1988-08-24 |
ATE69835T1 (de) | 1991-12-15 |
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