NO881505L - Fremgangsmaate til hindring eller unngaaelse av avleiringeri blandingsoppberedningssystemer for motorer. - Google Patents
Fremgangsmaate til hindring eller unngaaelse av avleiringeri blandingsoppberedningssystemer for motorer.Info
- Publication number
- NO881505L NO881505L NO881505A NO881505A NO881505L NO 881505 L NO881505 L NO 881505L NO 881505 A NO881505 A NO 881505A NO 881505 A NO881505 A NO 881505A NO 881505 L NO881505 L NO 881505L
- Authority
- NO
- Norway
- Prior art keywords
- groups
- unsubstituted
- alkyl
- group
- hydrocarbons
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 13
- 238000002360 preparation method Methods 0.000 title description 5
- 230000008021 deposition Effects 0.000 title 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000000446 fuel Substances 0.000 claims abstract description 47
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 35
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 34
- 229920005862 polyol Polymers 0.000 claims abstract description 24
- -1 polyol ethers Chemical class 0.000 claims abstract description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 11
- 239000000314 lubricant Substances 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 69
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 21
- 229920006395 saturated elastomer Polymers 0.000 claims description 19
- 150000003077 polyols Chemical class 0.000 claims description 17
- 125000003107 substituted aryl group Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 9
- 238000007792 addition Methods 0.000 claims description 8
- 150000001298 alcohols Chemical class 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 150000001735 carboxylic acids Chemical class 0.000 claims description 7
- 238000005260 corrosion Methods 0.000 claims description 7
- 230000007797 corrosion Effects 0.000 claims description 7
- 239000003112 inhibitor Substances 0.000 claims description 7
- 125000002619 bicyclic group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000000524 functional group Chemical group 0.000 claims description 6
- 125000002950 monocyclic group Chemical group 0.000 claims description 6
- 125000003080 thiophosphoric acid ester group Chemical group 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 3
- 125000000101 thioether group Chemical group 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000004036 acetal group Chemical group 0.000 claims 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 125000006325 2-propenyl amino group Chemical group [H]C([H])=C([H])C([H])([H])N([H])* 0.000 claims 1
- 125000004965 chloroalkyl group Chemical group 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 11
- 238000002474 experimental method Methods 0.000 description 10
- 229920000570 polyether Polymers 0.000 description 10
- 239000000654 additive Substances 0.000 description 8
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000006755 (C2-C20) alkyl group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- GBLQGXFTPLQBTA-UHFFFAOYSA-N 1,2,3-triazoline Chemical class C1CN=NN1 GBLQGXFTPLQBTA-UHFFFAOYSA-N 0.000 description 1
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical compound CCCCCOCCCCC AOPDRZXCEAKHHW-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
- JSIAIROWMJGMQZ-UHFFFAOYSA-N 2h-triazol-4-amine Chemical class NC1=CNN=N1 JSIAIROWMJGMQZ-UHFFFAOYSA-N 0.000 description 1
- OFECPMCOWSSDAR-UHFFFAOYSA-N 4,5-dihydrotriazol-1-amine Chemical class NN1CCN=N1 OFECPMCOWSSDAR-UHFFFAOYSA-N 0.000 description 1
- JJDGTGGQXAAVQX-UHFFFAOYSA-N 6-methyl-1-(6-methylheptoxy)heptane Chemical group CC(C)CCCCCOCCCCCC(C)C JJDGTGGQXAAVQX-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical class NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002913 oxalic acids Chemical class 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 125000000552 p-cresyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1O*)C([H])([H])[H] 0.000 description 1
- 229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000002270 phosphoric acid ester group Chemical group 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 150000003852 triazoles Chemical class 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
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/198—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid
- C10L1/1985—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/224—Amides; Imides carboxylic acid amides, imides
-
- 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
- C10L1/2462—Organic compounds containing sulfur, selenium and/or tellurium macromolecular compounds
- C10L1/2475—Organic compounds containing sulfur, selenium and/or tellurium macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon to carbon bonds
- C10L1/2487—Organic compounds containing sulfur, selenium and/or tellurium macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon to carbon bonds polyoxyalkylene thioethers (O + S 3=)
-
- 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)
- C10L1/2641—Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
-
- 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
- C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
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)
- Emergency Medicine (AREA)
- Combustion & Propulsion (AREA)
- Health & Medical Sciences (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Lubrication Details And Ventilation Of Internal Combustion Engines (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Superconductive Dynamoelectric Machines (AREA)
- Preliminary Treatment Of Fibers (AREA)
- Grinding-Machine Dressing And Accessory Apparatuses (AREA)
- Combustion Methods Of Internal-Combustion Engines (AREA)
- Accessories For Mixers (AREA)
- Cephalosporin Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19873711985 DE3711985A1 (de) | 1987-04-09 | 1987-04-09 | Verwendung von polyolethern zur verhinderung oder verminderung von ablagerungen in gemischaufbereitungssystemen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO881505D0 NO881505D0 (no) | 1988-04-07 |
| NO881505L true NO881505L (no) | 1988-10-10 |
Family
ID=6325221
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO881505A NO881505L (no) | 1987-04-09 | 1988-04-07 | Fremgangsmaate til hindring eller unngaaelse av avleiringeri blandingsoppberedningssystemer for motorer. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5024678A (fr) |
| EP (1) | EP0289785B1 (fr) |
| JP (1) | JPS649294A (fr) |
| CN (1) | CN1030253A (fr) |
| AT (1) | ATE64948T1 (fr) |
| AU (1) | AU602569B2 (fr) |
| DD (1) | DD284687A5 (fr) |
| DE (2) | DE3711985A1 (fr) |
| ES (1) | ES2004848B3 (fr) |
| FI (1) | FI881637A (fr) |
| GR (1) | GR880300184T1 (fr) |
| NO (1) | NO881505L (fr) |
| PL (1) | PL271720A1 (fr) |
| ZA (1) | ZA882249B (fr) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3826608A1 (de) * | 1988-08-05 | 1990-02-08 | Basf Ag | Polyetheramine oder polyetheraminderivate enthaltende kraftstoffe fuer ottomotoren |
| JPH02194089A (ja) * | 1989-01-20 | 1990-07-31 | Sanyo Chem Ind Ltd | メタノール燃料油用添加剤 |
| ES2017030A6 (es) * | 1989-07-26 | 1990-12-16 | Lascaray Sa | Composicion aditiva para gasolinas empleadas en vehiculos automoviles. |
| CA2020037A1 (fr) * | 1990-01-22 | 1991-07-23 | Rodney L. Sung | Composes d'ester polyoxyalkylene et compositions de carburant a moteur ori inhibe |
| JPH0662965B2 (ja) * | 1990-02-02 | 1994-08-17 | 花王株式会社 | 燃料油添加剤及び燃料油添加剤組成物 |
| US5197997A (en) * | 1990-11-29 | 1993-03-30 | The Lubrizol Corporation | Composition for use in diesel powered vehicles |
| GB9101884D0 (en) * | 1991-01-29 | 1991-03-13 | British Petroleum Co Plc | Fuel composition |
| US5286266A (en) * | 1992-07-09 | 1994-02-15 | Texaco Inc. | Motor fuel detergent additives - asymmetrical ureas of hydrocarbyloxypolyether amines and tertiary aminoalkyl primary amines |
| US5354343A (en) * | 1992-08-31 | 1994-10-11 | Shell Oil Company | Gasoline composition |
| US5366517A (en) * | 1992-12-18 | 1994-11-22 | Chevron Research And Technology Company | Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic ethers and poly(oxyalkylene) amines |
| US5366519A (en) * | 1992-12-18 | 1994-11-22 | Chevron Research And Technology Company | Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic esters and poly(oxyalkylene) amines |
| US5569310A (en) * | 1992-12-18 | 1996-10-29 | Chevron Chemical Company | Poly(oxyalkylene) hydroxyaromatic ethers and fuel compositions containing the same |
| US5462567A (en) * | 1992-12-28 | 1995-10-31 | Chevron Chemical Company | Fuel additive compositions containing poly(oxyalkylene)hydroxyaromatic esters and aliphatic amines |
| US5516342A (en) * | 1992-12-28 | 1996-05-14 | Chevron Chemical Company | Fuel additive compositions containing poly(oxyalkylene) hydroxyaromatic ethers and aliphatic amines |
| ATE177140T1 (de) * | 1993-12-13 | 1999-03-15 | Shell Int Research | Benzinzusammensetzung |
| US5441544A (en) * | 1993-12-23 | 1995-08-15 | Chevron Chemical Company | Fuel compositions containing substituted poly(oxyalkylene) aromatic ethers |
| US5538521A (en) * | 1993-12-23 | 1996-07-23 | Chevron Chemical Company | Fuel compositions containing polyalkyl and poly(oxyalkylene)aromatic esters |
| US5709718A (en) * | 1995-03-15 | 1998-01-20 | Shell Oil Company | Fuel compositions containing a polyether |
| TW477784B (en) * | 1996-04-26 | 2002-03-01 | Shell Int Research | Alkoxy acetic acid derivatives |
| SG55335A1 (en) * | 1996-06-28 | 1998-12-21 | Nippon Catalytic Chem Ind | Method for reducing deposition of cokes in heat-refining process of petroleum high-nolecular hydrocarbons and additive used in the method |
| US5746785A (en) * | 1997-07-07 | 1998-05-05 | Southwest Research Institute | Diesel fuel having improved qualities and method of forming |
| FR2797450B1 (fr) * | 1999-08-12 | 2002-12-06 | Inst Francais Du Petrole | Derives de polytetrahydrofuranne utilisables dans des compositions detergentes pour carburants de type essence |
| US6210452B1 (en) * | 2000-02-08 | 2001-04-03 | Hhntsman Petrochemical Corporation | Fuel additives |
| DE102004038113A1 (de) * | 2004-08-05 | 2006-03-16 | Basf Ag | Stickstoffhaltige heterocyclische Verbindungen als Reibverschleißvermindernder Zusatz zu Kraftstoffen |
| US8197560B2 (en) * | 2005-06-17 | 2012-06-12 | Kabushiki Kaisha Toshiba | Fuel for fuel cell, fuel cartridge for fuel cell and fuel cell |
| US20090172997A1 (en) * | 2008-01-04 | 2009-07-09 | Olah George A | Environmentally friendly ternary transportation flex-fuel of gasoline, methanol and bioethanol |
| EP2128232A1 (fr) * | 2008-05-20 | 2009-12-02 | Castrol Limited | Composition lubrifiante pour moteurs fonctionnant à l'éthanol |
| WO2010033441A1 (fr) * | 2008-09-16 | 2010-03-25 | The Lubrizol Corporation | Additif soluble dans un carburant de type alcool pour éliminer les dépôts dans des systèmes d'alimentation en carburant |
| CN102031178B (zh) * | 2010-12-24 | 2013-07-03 | 淄博润博化工销售有限公司 | 低硫柴油润滑性添加剂及其制备方法 |
| EP2726584B1 (fr) | 2011-06-30 | 2016-04-20 | ExxonMobil Research and Engineering Company | Procédé d'amélioration du point d'écoulement de compositions lubrifiantes contenant des monoéthers de polyalkylène glycol |
| WO2013003405A1 (fr) | 2011-06-30 | 2013-01-03 | Exxonmobil Research And Engineering Company | Compositions lubrifiantes contenant des monoéthers de polyalkylène glycol |
| US8586520B2 (en) | 2011-06-30 | 2013-11-19 | Exxonmobil Research And Engineering Company | Method of improving pour point of lubricating compositions containing polyalkylene glycol mono ethers |
| WO2013003394A1 (fr) | 2011-06-30 | 2013-01-03 | Exxonmobil Research And Engineering Company | Compositions lubrifiantes contenant des polyétheramines |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR761473A (fr) * | 1933-08-07 | 1934-03-20 | Carburants Speciaux Sa Des | Procédé de stabilisation, en présence de métaux tels que le cuivre, des produitsformés par l'introduction de composés organiques azotés dans les hydrocarbures tels que les essences de pétrole ou dans les mélanges d'essence et d'alcool |
| US2655440A (en) * | 1949-05-24 | 1953-10-13 | California Research Corp | Diesel fuel oil |
| US2763537A (en) * | 1949-05-24 | 1956-09-18 | California Research Corp | Diesel fuel oil |
| US2807526A (en) * | 1950-10-04 | 1957-09-24 | Standard Oil Co | Additive for motor fuels and fuel compositions containing the same |
| US2807525A (en) * | 1950-10-04 | 1957-09-24 | Standard Oil Co | Additive for motor fuels |
| GB708193A (en) * | 1951-05-08 | 1954-04-28 | Thompson Prod Inc | Improvements in or relating to fuel charges for internal combustion engines |
| US3440029A (en) * | 1964-05-20 | 1969-04-22 | Dow Chemical Co | Gasoline containing anti-icing additive |
| US3478096A (en) * | 1966-04-18 | 1969-11-11 | Universal Oil Prod Co | Sec.-alkyl- or cycloalkyl-alkoxy-alkylamines |
| US3849083A (en) * | 1972-04-14 | 1974-11-19 | Ethyl Corp | Gasoline additive |
| GB1403248A (en) * | 1972-10-27 | 1975-08-28 | British Petroleum Co | Amino ethers |
| US3980450A (en) * | 1973-10-23 | 1976-09-14 | The British Petroleum Company Limited | Gasoline composition |
| US4236020A (en) * | 1976-06-21 | 1980-11-25 | Chevron Research Company | Carbamate deposit control additives |
| SE404702B (sv) * | 1976-11-29 | 1978-10-23 | Svenska Metanol | Anvendning av en metanolbaserad komposition som dieselbrensle |
| BR8000889A (pt) * | 1979-02-21 | 1980-10-21 | Basf Ag | Composicoes carburantes para motores diesel |
| US4332594A (en) * | 1980-01-22 | 1982-06-01 | Chrysler Corporation | Fuels for internal combustion engines |
| US4464182A (en) * | 1981-03-31 | 1984-08-07 | Exxon Research & Engineering Co. | Glycol ester flow improver additive for distillate fuels |
| US4398921A (en) * | 1981-11-02 | 1983-08-16 | Ethyl Corporation | Gasohol compositions |
| US4409000A (en) * | 1981-12-14 | 1983-10-11 | The Lubrizol Corporation | Combinations of hydroxy amines and carboxylic dispersants as fuel additives |
| US4409001A (en) * | 1982-01-08 | 1983-10-11 | Texaco Inc. | Gasoline compositions containing amino alkanoic acids as detergents |
| US4427562A (en) * | 1982-05-06 | 1984-01-24 | Mobil Oil Corporation | Friction reducers for lubricants and fuels |
| SE8202879L (sv) * | 1982-05-07 | 1983-11-08 | Carbogel Ab | Vattenuppslamning av ett fast brensle samt sett och medel for framstellning derav |
| US4428354A (en) * | 1982-06-21 | 1984-01-31 | General Motors Corp. | Diesel engine fuel limiting system |
| GB2143846A (en) * | 1983-07-25 | 1985-02-20 | Shell Int Research | A diesel fuel based on methanol and/or ethanol |
| US4778481A (en) * | 1983-08-08 | 1988-10-18 | Chevron Research Company | Diesel fuel and method for deposit control in compression ignition engines |
| FR2552444A1 (fr) * | 1983-09-24 | 1985-03-29 | Sandoz Sa | Carburants pour moteurs a combustion interne contenant des inhibiteurs de corrosion |
| US4527996A (en) * | 1983-10-31 | 1985-07-09 | Chevron Research Company | Deposit control additives - hydroxy polyether polyamines |
| DE3343816C2 (de) * | 1983-12-03 | 1986-12-04 | UK Mineralölwerke Wenzel & Weidmann GmbH, 5180 Eschweiler | Schmiermittel |
| DE3412078A1 (de) * | 1984-03-31 | 1985-10-03 | Bayer Ag, 5090 Leverkusen | Zuendverbesserer fuer kraftstoffgemische |
| EP0166006A1 (fr) * | 1984-06-16 | 1986-01-02 | Union Rheinische Braunkohlen Kraftstoff Aktiengesellschaft | Combustible pour moteurs |
| DE3628504A1 (de) * | 1985-08-28 | 1987-03-12 | Liqui Moly Gmbh | Korrosionsinhibitor und diesen enthaltender treibstoff |
-
1987
- 1987-04-09 DE DE19873711985 patent/DE3711985A1/de active Granted
-
1988
- 1988-03-29 ZA ZA882249A patent/ZA882249B/xx unknown
- 1988-03-31 AT AT88105287T patent/ATE64948T1/de not_active IP Right Cessation
- 1988-03-31 ES ES88105287T patent/ES2004848B3/es not_active Expired - Lifetime
- 1988-03-31 DE DE8888105287T patent/DE3863477D1/de not_active Expired - Fee Related
- 1988-03-31 EP EP88105287A patent/EP0289785B1/fr not_active Expired - Lifetime
- 1988-04-05 US US07/177,623 patent/US5024678A/en not_active Expired - Fee Related
- 1988-04-07 NO NO881505A patent/NO881505L/no unknown
- 1988-04-08 FI FI881637A patent/FI881637A/fi not_active IP Right Cessation
- 1988-04-08 DD DD88314559A patent/DD284687A5/de not_active IP Right Cessation
- 1988-04-08 JP JP63085562A patent/JPS649294A/ja active Pending
- 1988-04-08 PL PL27172088A patent/PL271720A1/xx unknown
- 1988-04-09 CN CN88102090A patent/CN1030253A/zh active Pending
- 1988-04-11 AU AU14543/88A patent/AU602569B2/en not_active Ceased
-
1989
- 1989-06-22 GR GR88300184T patent/GR880300184T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU1454388A (en) | 1988-11-03 |
| FI881637A0 (fi) | 1988-04-08 |
| FI881637A (fi) | 1988-10-10 |
| AU602569B2 (en) | 1990-10-18 |
| GR880300184T1 (en) | 1989-06-22 |
| DE3863477D1 (de) | 1991-08-08 |
| ZA882249B (en) | 1988-10-03 |
| ES2004848B3 (es) | 1991-12-16 |
| US5024678A (en) | 1991-06-18 |
| PL271720A1 (en) | 1989-02-06 |
| DD284687A5 (de) | 1990-11-21 |
| DE3711985A1 (de) | 1988-10-20 |
| DE3711985C2 (fr) | 1992-02-27 |
| NO881505D0 (no) | 1988-04-07 |
| EP0289785A1 (fr) | 1988-11-09 |
| ATE64948T1 (de) | 1991-07-15 |
| JPS649294A (en) | 1989-01-12 |
| EP0289785B1 (fr) | 1991-07-03 |
| ES2004848A4 (es) | 1989-02-16 |
| CN1030253A (zh) | 1989-01-11 |
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