AU2004227095B2 - Fuel composition - Google Patents
Fuel composition Download PDFInfo
- Publication number
- AU2004227095B2 AU2004227095B2 AU2004227095A AU2004227095A AU2004227095B2 AU 2004227095 B2 AU2004227095 B2 AU 2004227095B2 AU 2004227095 A AU2004227095 A AU 2004227095A AU 2004227095 A AU2004227095 A AU 2004227095A AU 2004227095 B2 AU2004227095 B2 AU 2004227095B2
- Authority
- AU
- Australia
- Prior art keywords
- fuel
- gasoline fuel
- composition according
- mono
- groups
- 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
- 239000000446 fuel Substances 0.000 title claims description 82
- 239000000203 mixture Substances 0.000 title claims description 43
- 239000000654 additive Substances 0.000 claims description 44
- 239000002816 fuel additive Substances 0.000 claims description 22
- 229920002367 Polyisobutene Polymers 0.000 claims description 20
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 19
- -1 alkaline earth metal salts Chemical class 0.000 claims description 18
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 18
- 230000000996 additive effect Effects 0.000 claims description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
- 230000009471 action Effects 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 12
- 239000003599 detergent Substances 0.000 claims description 12
- 229910052783 alkali metal Inorganic materials 0.000 claims description 11
- 150000001340 alkali metals Chemical class 0.000 claims description 11
- 239000007795 chemical reaction product Substances 0.000 claims description 11
- 230000002401 inhibitory effect Effects 0.000 claims description 11
- 229920000768 polyamine Polymers 0.000 claims description 11
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 7
- 229910021529 ammonia Inorganic materials 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 150000002989 phenols Chemical class 0.000 claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 230000002209 hydrophobic effect Effects 0.000 claims description 4
- 229920001083 polybutene Polymers 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 238000006268 reductive amination reaction Methods 0.000 claims description 4
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 3
- 238000006683 Mannich reaction Methods 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 150000001733 carboxylic acid esters Chemical group 0.000 claims description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 150000002924 oxiranes Chemical class 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 229940014800 succinic anhydride Drugs 0.000 claims description 3
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 3
- 150000003628 tricarboxylic acids Chemical class 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 1
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 description 8
- 239000002199 base oil Substances 0.000 description 7
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 6
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 238000005576 amination reaction Methods 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 3
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 235000013847 iso-butane Nutrition 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical class CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- UZVAZDQMPUOHKP-UHFFFAOYSA-N 2-(7-methyloctyl)phenol Chemical compound CC(C)CCCCCCC1=CC=CC=C1O UZVAZDQMPUOHKP-UHFFFAOYSA-N 0.000 description 1
- TZGPACAKMCUCKX-UHFFFAOYSA-N 2-hydroxyacetamide Chemical class NC(=O)CO TZGPACAKMCUCKX-UHFFFAOYSA-N 0.000 description 1
- WPMYUUITDBHVQZ-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoic acid Chemical compound CC(C)(C)C1=CC(CCC(O)=O)=CC(C(C)(C)C)=C1O WPMYUUITDBHVQZ-UHFFFAOYSA-N 0.000 description 1
- ANHQLUBMNSSPBV-UHFFFAOYSA-N 4h-pyrido[3,2-b][1,4]oxazin-3-one Chemical group C1=CN=C2NC(=O)COC2=C1 ANHQLUBMNSSPBV-UHFFFAOYSA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 1
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229950003621 butoxylate Drugs 0.000 description 1
- MQWDTXAOPTYTLC-UHFFFAOYSA-N butyl 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylate Chemical compound C1CC(C(=O)OCCCC)(C=2C=CC=CC=2)CCN1CCC(C#N)(C=1C=CC=CC=1)C1=CC=CC=C1 MQWDTXAOPTYTLC-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 229920013639 polyalphaolefin Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
Classifications
-
- 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
-
- 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
- C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear
-
- 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
- C10L1/143—Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
-
- 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
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
-
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
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)
- Combustion & Propulsion (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10316871A DE10316871A1 (de) | 2003-04-11 | 2003-04-11 | Kraftstoffzusammensetzung |
| DE10316871.0 | 2003-04-11 | ||
| PCT/EP2004/003811 WO2004090079A1 (de) | 2003-04-11 | 2004-04-08 | Kraftstoffzusammensetzung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2004227095A1 AU2004227095A1 (en) | 2004-10-21 |
| AU2004227095B2 true AU2004227095B2 (en) | 2010-07-15 |
Family
ID=33016286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2004227095A Expired AU2004227095B2 (en) | 2003-04-11 | 2004-04-08 | Fuel composition |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US20060196110A1 (ko) |
| EP (3) | EP1615985B1 (ko) |
| JP (3) | JP4452712B2 (ko) |
| KR (2) | KR101320732B1 (ko) |
| CN (1) | CN100545244C (ko) |
| AR (1) | AR044001A1 (ko) |
| AU (1) | AU2004227095B2 (ko) |
| BR (1) | BRPI0409171A (ko) |
| CA (2) | CA2520578C (ko) |
| CL (1) | CL2004000766A1 (ko) |
| DE (1) | DE10316871A1 (ko) |
| DK (1) | DK1615985T3 (ko) |
| ES (1) | ES2443993T3 (ko) |
| MX (1) | MXPA05010183A (ko) |
| MY (1) | MY162483A (ko) |
| NO (1) | NO20054374L (ko) |
| PL (2) | PL2270119T3 (ko) |
| PT (1) | PT1615985E (ko) |
| RU (1) | RU2005134823A (ko) |
| SI (1) | SI1615985T1 (ko) |
| WO (1) | WO2004090079A1 (ko) |
| ZA (1) | ZA200509086B (ko) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10316871A1 (de) | 2003-04-11 | 2004-10-21 | Basf Ag | Kraftstoffzusammensetzung |
| US20080086936A1 (en) * | 2006-10-16 | 2008-04-17 | Cunningham Lawrence J | Method and compositions for reducing wear in engines combusting ethanol-containing fuels |
| US20080086934A1 (en) * | 2006-10-16 | 2008-04-17 | Cunningham Lawrence J | Protecting fuel delivery systems in engines combusting ethanol-containing fuels |
| US20080086935A1 (en) * | 2006-10-16 | 2008-04-17 | Lawrence J Cunningham | Method and compositions for reducing corrosion in engines combusting ethanol-containing fuels |
| US20080086933A1 (en) * | 2006-10-16 | 2008-04-17 | Cunningham Lawrence J | Volatility agents as fuel additives for ethanol-containing fuels |
| US20080168708A1 (en) * | 2007-01-11 | 2008-07-17 | Cunningham Lawrence J | Method and compositions for reducing deposits in engines combusting ethanol-containing fuels and a corrosion inhibitor |
| JP2011511859A (ja) | 2008-02-01 | 2011-04-14 | ビーエーエスエフ ソシエタス・ヨーロピア | 特殊なポリイソブテンアミンおよび燃料中の洗剤としての該化合物の使用 |
| GB0903165D0 (en) * | 2009-02-25 | 2009-04-08 | Innospec Ltd | Methods and uses relating to fuel compositions |
| KR20130095660A (ko) * | 2010-06-01 | 2013-08-28 | 바스프 에스이 | 분산제 부스터로서 저분자량의 폴리이소부틸-치환된 아민 |
| JP2014501813A (ja) | 2010-12-02 | 2014-01-23 | ビーエーエスエフ ソシエタス・ヨーロピア | ヒドロカルビルで置換されたジカルボン酸と窒素化合物とからの反応生成物の、燃料消費量の低減のための使用 |
| EP2554636A1 (en) * | 2011-08-03 | 2013-02-06 | Innospec Limited | Fuel compositions |
| US20150113867A1 (en) | 2013-10-24 | 2015-04-30 | Basf Se | Use of an alkoxylated polytetrahydrofuran to reduce fuel consumption |
| US20150113864A1 (en) | 2013-10-24 | 2015-04-30 | Basf Se | Use of a complex ester to reduce fuel consumption |
| US20150113859A1 (en) | 2013-10-24 | 2015-04-30 | Basf Se | Use of polyalkylene glycol to reduce fuel consumption |
| JP6216883B2 (ja) | 2013-11-18 | 2017-10-18 | アフトン・ケミカル・コーポレーションＡｆｔｏｎ Ｃｈｅｍｉｃａｌ Ｃｏｒｐｏｒａｔｉｏｎ | 吸気弁沈着物制御用の混合洗浄剤組成物 |
| MY180330A (en) * | 2014-01-29 | 2020-11-28 | Basf Se | Use of polycarboxylic-acid-based additives for fuels |
| EP3099768B1 (de) * | 2014-01-29 | 2019-08-21 | Basf Se | Korrosionsinhibitoren für kraftstoffe |
| US9249769B1 (en) * | 2015-03-24 | 2016-02-02 | Afton Chemical Corporation | Fuel additives for treating internal deposits of fuel injectors |
| US11078418B2 (en) | 2016-07-05 | 2021-08-03 | Basf Se | Corrosion inhibitors for fuels and lubricants |
| RU2019122807A (ru) | 2016-12-20 | 2021-01-22 | Басф Се | Применение смеси комплексного сложного эфира с монокарбоновой кислотой для уменьшения трения |
| US10273425B2 (en) | 2017-03-13 | 2019-04-30 | Afton Chemical Corporation | Polyol carrier fluids and fuel compositions including polyol carrier fluids |
| CN110494534A (zh) * | 2017-04-11 | 2019-11-22 | 巴斯夫欧洲公司 | 用作燃料添加剂的烷氧基化胺 |
| KR20210127323A (ko) | 2020-04-14 | 2021-10-22 | 정재훈 | 애완견 배변기 |
| GB202111108D0 (en) * | 2021-08-02 | 2021-09-15 | Innospec Ltd | Compositions, and methods and uses relating thereto |
| US11873461B1 (en) | 2022-09-22 | 2024-01-16 | Afton Chemical Corporation | Extreme pressure additives with improved copper corrosion |
| US12024686B2 (en) | 2022-09-30 | 2024-07-02 | Afton Chemical Corporation | Gasoline additive composition for improved engine performance |
| US11884890B1 (en) | 2023-02-07 | 2024-01-30 | Afton Chemical Corporation | Gasoline additive composition for improved engine performance |
| US11795412B1 (en) | 2023-03-03 | 2023-10-24 | Afton Chemical Corporation | Lubricating composition for industrial gear fluids |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11209765A (ja) * | 1998-01-26 | 1999-08-03 | Yoshitake Nakada | ガソリン用添加剤及びガソリン |
| WO2001085874A2 (de) * | 2000-05-05 | 2001-11-15 | Basf Aktiengesellschaft | Kraftstoffadditivpakete für ottokraftstoffe mit verbesserten viskositätseigenschaften und guter ivd performance |
| WO2003074637A1 (de) * | 2002-03-06 | 2003-09-12 | Basf Aktiengesellschaft | Kraftstoffadditivgemisch für ottokraftstoffe mit synergistischer ivd-performance |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD140359A1 (de) * | 1978-12-13 | 1980-02-27 | Alfred Boczek | Bleiarme treibstoffzusammensetzung fuer ottomotoren |
| DE3116734C2 (de) * | 1981-04-28 | 1985-07-25 | Veba Oel AG, 4650 Gelsenkirchen | Vergaserkraftstoff |
| US4444166A (en) * | 1981-06-16 | 1984-04-24 | Kovacs Research Center, Inc. | Method and apparatus for reducing the operating compression ratios of compression ignition engines |
| US4398921A (en) | 1981-11-02 | 1983-08-16 | Ethyl Corporation | Gasohol compositions |
| US4690687A (en) | 1985-08-16 | 1987-09-01 | The Lubrizol Corporation | Fuel products comprising a lead scavenger |
| DE3611230A1 (de) | 1986-04-04 | 1987-10-08 | Basf Ag | Polybutyl- und polyisobutylamine, verfahren zu deren herstellung und diese enthaltende kraft- und schmierstoffzusammensetzungen |
| EP0307815B1 (de) | 1987-09-15 | 1992-04-08 | BASF Aktiengesellschaft | Kraftstoffe für Ottomotoren |
| DE3732908A1 (de) | 1987-09-30 | 1989-04-13 | Basf Ag | Polyetheramine enthaltende kraftstoffe fuer ottomotoren |
| US4877416A (en) * | 1987-11-18 | 1989-10-31 | Chevron Research Company | Synergistic fuel compositions |
| US4849572A (en) | 1987-12-22 | 1989-07-18 | Exxon Chemical Patents Inc. | Process for preparing polybutenes having enhanced reactivity using boron trifluoride catalysts (PT-647) |
| DE3826608A1 (de) | 1988-08-05 | 1990-02-08 | Basf Ag | Polyetheramine oder polyetheraminderivate enthaltende kraftstoffe fuer ottomotoren |
| DE3838918A1 (de) * | 1988-11-17 | 1990-05-23 | Basf Ag | Kraftstoffe fuer verbrennungsmaschinen |
| US5089028A (en) | 1990-08-09 | 1992-02-18 | Mobil Oil Corporation | Deposit control additives and fuel compositions containing the same |
| DE4030164A1 (de) | 1990-09-24 | 1992-03-26 | Basf Ag | Kraftstoffe fuer verbrennungsmotoren und schmierstoffe enthaltende hochmolekulare aminoalkohole |
| JPH06128573A (ja) * | 1992-05-28 | 1994-05-10 | Nippon Oil Co Ltd | ガソリン組成物 |
| DE4313088A1 (de) | 1993-04-22 | 1994-10-27 | Basf Ag | Poly-1-n-alkenamine und diese enthaltende Kraft- und Schmierstoffzusammensetzungen |
| AT400149B (de) | 1993-08-17 | 1995-10-25 | Oemv Ag | Additiv für unverbleite ottokraftstoffe sowie dieses enthaltender kraftstoff |
| CA2194572A1 (en) | 1994-05-31 | 1995-12-07 | William C. Orr | Vapor phase combustion methods and compositions |
| DE4425834A1 (de) | 1994-07-21 | 1996-01-25 | Basf Ag | Umsetzungsprodukte aus Polyisobutenen und Stickoxiden oder Gemischen aus Stickoxiden und Sauerstoff und ihre Verwendung als Kraft- und Schmierstoffadditive |
| DE4425835A1 (de) | 1994-07-21 | 1996-01-25 | Basf Ag | Verwendung von Umsetzungsprodukten aus Polyolefinen und Stickoxiden oder Gemischen aus Stickoxiden und Sauerstoff als Additive für Kraftstoffe |
| DE4432038A1 (de) | 1994-09-09 | 1996-03-14 | Basf Ag | Polyetheramine enthaltende Kraftstoffe für Ottomotoren |
| US5679118A (en) | 1995-02-08 | 1997-10-21 | Research Octane Inc. | Refining process and apparatus |
| DE19525938A1 (de) | 1995-07-17 | 1997-01-23 | Basf Ag | Verfahren zur Herstellung von organischen Stickstoffverbindungen, spezielle organische Stickstoffverbindungen und Mischungen aus solchen Verbindungen sowie deren Verwendung als Kraft- und Schmierstoffadditive |
| US5752990A (en) | 1996-03-29 | 1998-05-19 | Exxon Research And Engineering Company | Composition and method for reducing combustion chamber deposits, intake valve deposits or both in spark ignition internal combustion engines |
| DE19620262A1 (de) | 1996-05-20 | 1997-11-27 | Basf Ag | Verfahren zur Herstellung von Polyalkenaminen |
| US5725612A (en) | 1996-06-07 | 1998-03-10 | Ethyl Corporation | Additives for minimizing intake valve deposits, and their use |
| GB9618546D0 (en) | 1996-09-05 | 1996-10-16 | Bp Chemicals Additives | Dispersants/detergents for hydrocarbons fuels |
| JP3948796B2 (ja) | 1997-09-30 | 2007-07-25 | 新日本石油株式会社 | 筒内直接噴射式ガソリンエンジン用無鉛ガソリン |
| DE19830818A1 (de) * | 1998-07-09 | 2000-01-13 | Basf Ag | Propoxilat enthaltende Kraftstoffzusammensetzungen |
| DE19905211A1 (de) * | 1999-02-09 | 2000-08-10 | Basf Ag | Kraftstoffzusammensetzung |
| US6193767B1 (en) | 1999-09-28 | 2001-02-27 | The Lubrizol Corporation | Fuel additives and fuel compositions comprising said fuel additives |
| DK1250404T3 (da) | 1999-12-13 | 2009-06-22 | Afton Chemical Intangibles Llc | Fremgangsmåde til kontrol af injektoraflejringer i benzinmotorer med direkte indspröjtning under anvendelse af en brændstofsammensætning indeholdende et Mannich-base-detergent |
| DE10109260A1 (de) | 2001-02-26 | 2002-09-05 | Basf Ag | Ottokraftstoffadditivzusammensetzung zur Erhöhung der Motoroktanzahl |
| DE10123553A1 (de) * | 2001-05-15 | 2002-11-21 | Basf Ag | Verfahren zur Herstellung von Polyalkenylsuccinimidprodukten, neue Polyalkenylsuccinimidprodukte mit verbesserten Eigenschaften, Zwischenprodukte und Verwendungen |
| US20030029077A1 (en) | 2001-08-07 | 2003-02-13 | The Lubrizol Corporation, A Corporation Of The State Of Ohio | Fuel composition containing detergent combination and methods thereof |
| DE60307060T2 (de) * | 2002-03-14 | 2007-02-15 | Shell Internationale Research Maatschappij B.V. | Ottokraftstoffadditive |
| DE10316871A1 (de) | 2003-04-11 | 2004-10-21 | Basf Ag | Kraftstoffzusammensetzung |
-
2003
- 2003-04-11 DE DE10316871A patent/DE10316871A1/de not_active Withdrawn
-
2004
- 2004-03-29 MY MYPI20041114A patent/MY162483A/en unknown
- 2004-04-07 AR ARP040101182A patent/AR044001A1/es active IP Right Grant
- 2004-04-08 KR KR1020127014391A patent/KR101320732B1/ko active IP Right Grant
- 2004-04-08 WO PCT/EP2004/003811 patent/WO2004090079A1/de active Search and Examination
- 2004-04-08 SI SI200432123T patent/SI1615985T1/sl unknown
- 2004-04-08 KR KR1020057018049A patent/KR101186408B1/ko active IP Right Grant
- 2004-04-08 RU RU2005134823/04A patent/RU2005134823A/ru unknown
- 2004-04-08 CA CA2520578A patent/CA2520578C/en not_active Expired - Lifetime
- 2004-04-08 PL PL10180913T patent/PL2270119T3/pl unknown
- 2004-04-08 CL CL200400766A patent/CL2004000766A1/es unknown
- 2004-04-08 BR BRPI0409171-0A patent/BRPI0409171A/pt not_active Application Discontinuation
- 2004-04-08 AU AU2004227095A patent/AU2004227095B2/en not_active Expired
- 2004-04-08 EP EP04726498.1A patent/EP1615985B1/de not_active Revoked
- 2004-04-08 PT PT47264981T patent/PT1615985E/pt unknown
- 2004-04-08 JP JP2006505086A patent/JP4452712B2/ja not_active Expired - Fee Related
- 2004-04-08 DK DK04726498.1T patent/DK1615985T3/en active
- 2004-04-08 CN CNB2004800097618A patent/CN100545244C/zh not_active Expired - Lifetime
- 2004-04-08 EP EP20174630.2A patent/EP3736317A1/de not_active Withdrawn
- 2004-04-08 ES ES04726498.1T patent/ES2443993T3/es not_active Expired - Lifetime
- 2004-04-08 CA CA2810284A patent/CA2810284C/en not_active Expired - Lifetime
- 2004-04-08 US US10/551,239 patent/US20060196110A1/en not_active Abandoned
- 2004-04-08 PL PL04726498T patent/PL1615985T3/pl unknown
- 2004-04-08 EP EP10180913.5A patent/EP2270119B1/de not_active Revoked
- 2004-04-08 MX MXPA05010183A patent/MXPA05010183A/es active IP Right Grant
-
2005
- 2005-09-21 NO NO20054374A patent/NO20054374L/no not_active Application Discontinuation
- 2005-11-10 ZA ZA200509086A patent/ZA200509086B/xx unknown
-
2009
- 2009-10-19 JP JP2009240064A patent/JP2010013665A/ja active Pending
-
2013
- 2013-06-10 JP JP2013121995A patent/JP2013209664A/ja active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11209765A (ja) * | 1998-01-26 | 1999-08-03 | Yoshitake Nakada | ガソリン用添加剤及びガソリン |
| WO2001085874A2 (de) * | 2000-05-05 | 2001-11-15 | Basf Aktiengesellschaft | Kraftstoffadditivpakete für ottokraftstoffe mit verbesserten viskositätseigenschaften und guter ivd performance |
| WO2003074637A1 (de) * | 2002-03-06 | 2003-09-12 | Basf Aktiengesellschaft | Kraftstoffadditivgemisch für ottokraftstoffe mit synergistischer ivd-performance |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2004227095B2 (en) | Fuel composition | |
| AU766424B2 (en) | Fuel composition | |
| KR101218902B1 (ko) | 마모 감소를 위한 연료 첨가제로서의 함질소 복소환식화합물 | |
| JP4268632B2 (ja) | 改善された適用特性を有するポリアルケンアミン | |
| CA2406762C (en) | Fuel additive packets for gasoline fuels having improved viscosity properties and good ivd performance | |
| CA2478643C (en) | Fuel additive mixtures for gasoline fuels with synergistic ivd performance | |
| US20050044779A1 (en) | Fuel composition | |
| MXPA01007942A (en) | Fuel composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |