NO325567B1 - Anvendelse av brennstoff-tilsetningsmidler - Google Patents
Anvendelse av brennstoff-tilsetningsmidler Download PDFInfo
- Publication number
- NO325567B1 NO325567B1 NO19985533A NO985533A NO325567B1 NO 325567 B1 NO325567 B1 NO 325567B1 NO 19985533 A NO19985533 A NO 19985533A NO 985533 A NO985533 A NO 985533A NO 325567 B1 NO325567 B1 NO 325567B1
- Authority
- NO
- Norway
- Prior art keywords
- fuel
- fuels
- lubricity
- formula
- additives
- Prior art date
Links
- 239000002816 fuel additive Substances 0.000 title description 10
- 239000000446 fuel Substances 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 239000010763 heavy fuel oil Substances 0.000 claims description 2
- -1 petrol Substances 0.000 claims description 2
- 239000003350 kerosene Substances 0.000 claims 1
- 239000000654 additive Substances 0.000 description 20
- 238000005260 corrosion Methods 0.000 description 19
- 230000007797 corrosion Effects 0.000 description 16
- 238000012360 testing method Methods 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 230000003993 interaction Effects 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000008064 anhydrides Chemical class 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000009849 deactivation Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- 238000000605 extraction 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
- 239000003879 lubricant additive Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 235000011044 succinic acid Nutrition 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-M 9-cis,12-cis-Octadecadienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC([O-])=O OYHQOLUKZRVURQ-HZJYTTRNSA-M 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-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
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000003178 carboxy group Chemical class [H]OC(*)=O 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000893 inhibin Substances 0.000 description 1
- ZPNFWUPYTFPOJU-LPYSRVMUSA-N iniprol Chemical compound C([C@H]1C(=O)NCC(=O)NCC(=O)N[C@H]2CSSC[C@H]3C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](C(N[C@H](C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC=4C=CC=CC=4)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=4C=CC=CC=4)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC2=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H]2N(CCC2)C(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N2[C@@H](CCC2)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N2[C@@H](CCC2)C(=O)N3)C(=O)NCC(=O)NCC(=O)N[C@@H](C)C(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@H](C(=O)N1)C(C)C)[C@@H](C)O)[C@@H](C)CC)=O)[C@@H](C)CC)C1=CC=C(O)C=C1 ZPNFWUPYTFPOJU-LPYSRVMUSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229940049918 linoleate Drugs 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- HPZHFGBKCGWNGN-UHFFFAOYSA-N n-benzyl-2-methyl-7h-pyrrolo[2,3-d]pyrimidin-4-amine Chemical compound C=12C=CNC2=NC(C)=NC=1NCC1=CC=CC=C1 HPZHFGBKCGWNGN-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 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
-
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/593—Dicarboxylic acid esters having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G75/00—Inhibiting corrosion or fouling in apparatus for treatment or conversion of hydrocarbon oils, in general
- C10G75/02—Inhibiting corrosion or fouling in apparatus for treatment or conversion of hydrocarbon oils, in general by addition of corrosion inhibitors
-
- 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
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
- C10L1/191—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polyhydroxyalcohols
-
- 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
-
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Emergency Medicine (AREA)
- Health & Medical Sciences (AREA)
- Combustion & Propulsion (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9611406A GB9611406D0 (en) | 1996-05-31 | 1996-05-31 | Fuel additives |
| GB9619701A GB9619701D0 (en) | 1996-09-20 | 1996-09-20 | Fuel additives |
| PCT/GB1997/001469 WO1997045507A1 (en) | 1996-05-31 | 1997-05-30 | Fuel additives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO985533D0 NO985533D0 (no) | 1998-11-27 |
| NO985533L NO985533L (no) | 1999-01-27 |
| NO325567B1 true NO325567B1 (no) | 2008-06-23 |
Family
ID=26309418
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19985533A NO325567B1 (no) | 1996-05-31 | 1998-11-27 | Anvendelse av brennstoff-tilsetningsmidler |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US6156082A (hu) |
| EP (1) | EP0902824B1 (hu) |
| JP (1) | JP3532217B2 (hu) |
| KR (1) | KR100337275B1 (hu) |
| AR (1) | AR007355A1 (hu) |
| AT (1) | ATE276336T1 (hu) |
| AU (1) | AU714140B2 (hu) |
| BR (1) | BR9709272A (hu) |
| CA (1) | CA2256725C (hu) |
| CZ (1) | CZ295788B6 (hu) |
| DE (1) | DE69730709T2 (hu) |
| DK (1) | DK0902824T3 (hu) |
| ES (1) | ES2229353T3 (hu) |
| HU (1) | HUP9902408A3 (hu) |
| IL (1) | IL126985A (hu) |
| NO (1) | NO325567B1 (hu) |
| NZ (1) | NZ333310A (hu) |
| PL (1) | PL189588B1 (hu) |
| PT (1) | PT902824E (hu) |
| SI (1) | SI0902824T1 (hu) |
| SK (1) | SK284524B6 (hu) |
| TR (1) | TR199802455T2 (hu) |
| WO (1) | WO1997045507A1 (hu) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10000649C2 (de) | 2000-01-11 | 2001-11-29 | Clariant Gmbh | Mehrfunktionelles Additiv für Brennstofföle |
| EP1116780B1 (de) | 2000-01-11 | 2005-08-31 | Clariant GmbH | Mehrfunktionelles Additiv für Brennstofföle |
| DE10000650C2 (de) * | 2000-01-11 | 2003-04-10 | Clariant Gmbh | Mehrfunktionelles Additiv für Brennstofföle |
| AU3232901A (en) | 2000-02-16 | 2001-08-27 | Teijin Limited | Meta-form wholly aromatic polyamide fiber and process for producing the same |
| DE10012946B4 (de) * | 2000-03-16 | 2006-02-02 | Clariant Gmbh | Verwendung von öllöslichen Amphiphilen als Lösemittel für hydroxyfunktionelle Copolymere |
| AR028780A1 (es) * | 2000-07-03 | 2003-05-21 | Ass Octel | Un metodo para incrementar la lubricidad de un combustible de hidrocarbonado liquido; la composicion de aditivo y el compuesto utilizado |
| US7182795B2 (en) * | 2002-03-13 | 2007-02-27 | Atton Chemical Intangibles Llc | Fuel lubricity additives derived from hydrocarbyl succinic anhydrides and hydroxy amines, and middle distillate fuels containing same |
| WO2004024850A1 (en) * | 2002-09-13 | 2004-03-25 | Octel Starreon Llc | Process for the production of a fuel composition |
| US20040167610A1 (en) * | 2003-02-26 | 2004-08-26 | Fleming James A. | Locking stent |
| EP1512736B1 (en) | 2003-09-05 | 2018-05-02 | Infineum International Limited | Stabilised diesel fuel additive compositions |
| US20050132641A1 (en) * | 2003-12-23 | 2005-06-23 | Mccallum Andrew J. | Fuel lubricity from blends of lubricity improvers and corrosion inhibitors or stability additives |
| DE102004038113A1 (de) | 2004-08-05 | 2006-03-16 | Basf Ag | Stickstoffhaltige heterocyclische Verbindungen als Reibverschleißvermindernder Zusatz zu Kraftstoffen |
| EP1640438B1 (en) | 2004-09-17 | 2017-08-30 | Infineum International Limited | Improvements in Fuel Oils |
| CA2520174C (en) | 2004-09-17 | 2013-07-23 | Infineum International Limited | Additive composition for improving conductivity in fuel oils |
| EP1669433A1 (en) * | 2004-12-13 | 2006-06-14 | Basf Aktiengesellschaft | Hydrocarbyl succinic acid and hydrocarbylsuccinic acid derivatives as friction modifiers |
| US20060130394A1 (en) * | 2004-12-22 | 2006-06-22 | Flint Hills Resources, L.P. | Performance diesel fuels and additives |
| FR2888248B1 (fr) * | 2005-07-05 | 2010-02-12 | Total France | Composition lubrifiante pour melange hydrocarbone et produits obtenus |
| GB0515998D0 (en) * | 2005-08-03 | 2005-09-07 | Ass Octel | Fuel additives |
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| US8250931B2 (en) * | 2008-03-28 | 2012-08-28 | Global Process Technologies, Inc. | Methods and compositions for inhibiting corrosion in non-aqueous, non-conductive liquids |
| JP2012528218A (ja) * | 2009-05-25 | 2012-11-12 | 昭和シェル石油株式会社 | ガソリン組成物 |
| WO2010136437A1 (en) * | 2009-05-25 | 2010-12-02 | Shell Internationale Research Maatschappij B.V. | Gasoline compositions |
| DE102009060389A1 (de) * | 2009-12-24 | 2011-06-30 | Clariant International Ltd. | Kälteadditive mit verbesserter Fließfähigkeit |
| US8557002B2 (en) | 2010-11-12 | 2013-10-15 | Baker Hughes Incorporated | Fuel additives for enhanced lubricity and anti-corrosion properties |
| US20120304531A1 (en) | 2011-05-30 | 2012-12-06 | Shell Oil Company | Liquid fuel compositions |
| US9476005B1 (en) | 2013-05-24 | 2016-10-25 | Greyrock Energy, Inc. | High-performance diesel fuel lubricity additive |
| WO2017144378A1 (de) | 2016-02-23 | 2017-08-31 | Basf Se | HYDROPHOBE POLYCARBONSÄUREN ALS REIBVERSCHLEIß-VERMINDERNDER ZUSATZ ZU KRAFTSTOFFEN |
| EP4339264A3 (en) | 2017-03-30 | 2024-06-12 | Innospec Limited | Method and use |
| GB201705088D0 (en) * | 2017-03-30 | 2017-05-17 | Innospec Ltd | Composition, method and use |
| KR20210001025U (ko) | 2019-11-04 | 2021-05-12 | 대우조선해양 주식회사 | 캔 압착 장치 |
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| US3045042A (en) * | 1957-08-16 | 1962-07-17 | Monsanto Chemicals | Acid polyester succinates |
| US2993773A (en) * | 1959-02-02 | 1961-07-25 | Petrolite Corp | Ester additives |
| NL134315C (hu) * | 1962-10-04 | |||
| DE1271877B (de) * | 1963-04-23 | 1968-07-04 | Lubrizol Corp | Schmieroel |
| US3273981A (en) * | 1963-07-16 | 1966-09-20 | Exxon Research Engineering Co | Anti-wear oil additives |
| US3287273A (en) * | 1965-09-09 | 1966-11-22 | Exxon Research Engineering Co | Lubricity additive-hydrogenated dicarboxylic acid and a glycol |
| DE2029804A1 (de) * | 1969-06-16 | 1970-12-23 | The Lubrizol Corp., Cleveland, Ohio (V.St.A.) | Verwendung einer Zusatz-Kombination für Kohlenwasserstoffe |
| FR2169718B1 (hu) * | 1971-12-31 | 1974-09-13 | Inst Francais Du Petrole | |
| US4129508A (en) * | 1977-10-13 | 1978-12-12 | The Lubrizol Corporation | Demulsifier additive compositions for lubricants and fuels and concentrates containing the same |
| US4216114A (en) * | 1977-11-18 | 1980-08-05 | Imperial Chemical Industries Limited | Demulsification process |
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| US5080817A (en) * | 1990-09-18 | 1992-01-14 | Nalco Chemical Company | Corrosion inhibitor for 2-cycle engine oils comprising dodecenyl succinic anhydride-propylene glycol esters |
| GB9301119D0 (en) * | 1993-01-21 | 1993-03-10 | Exxon Chemical Patents Inc | Fuel composition |
-
1997
- 1997-05-30 ES ES97924135T patent/ES2229353T3/es not_active Expired - Lifetime
- 1997-05-30 HU HU9902408A patent/HUP9902408A3/hu unknown
- 1997-05-30 PL PL97330224A patent/PL189588B1/pl unknown
- 1997-05-30 CA CA002256725A patent/CA2256725C/en not_active Expired - Lifetime
- 1997-05-30 AU AU29703/97A patent/AU714140B2/en not_active Ceased
- 1997-05-30 WO PCT/GB1997/001469 patent/WO1997045507A1/en active Search and Examination
- 1997-05-30 IL IL12698597A patent/IL126985A/en not_active IP Right Cessation
- 1997-05-30 EP EP97924135A patent/EP0902824B1/en not_active Expired - Lifetime
- 1997-05-30 TR TR1998/02455T patent/TR199802455T2/xx unknown
- 1997-05-30 US US09/194,357 patent/US6156082A/en not_active Expired - Lifetime
- 1997-05-30 CZ CZ19983911A patent/CZ295788B6/cs not_active IP Right Cessation
- 1997-05-30 SI SI9730681T patent/SI0902824T1/xx unknown
- 1997-05-30 DE DE69730709T patent/DE69730709T2/de not_active Expired - Lifetime
- 1997-05-30 SK SK1648-98A patent/SK284524B6/sk not_active IP Right Cessation
- 1997-05-30 DK DK97924135T patent/DK0902824T3/da active
- 1997-05-30 AR ARP970102348A patent/AR007355A1/es active IP Right Grant
- 1997-05-30 BR BR9709272A patent/BR9709272A/pt not_active IP Right Cessation
- 1997-05-30 PT PT97924135T patent/PT902824E/pt unknown
- 1997-05-30 KR KR1019980709702A patent/KR100337275B1/ko not_active IP Right Cessation
- 1997-05-30 JP JP54186897A patent/JP3532217B2/ja not_active Expired - Fee Related
- 1997-05-30 NZ NZ333310A patent/NZ333310A/en unknown
- 1997-05-30 AT AT97924135T patent/ATE276336T1/de active
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1998
- 1998-11-27 NO NO19985533A patent/NO325567B1/no not_active IP Right Cessation
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