JP2001503081A - 燃料および燃料組成物用の洗浄および耐食性添加剤 - Google Patents
燃料および燃料組成物用の洗浄および耐食性添加剤Info
- Publication number
- JP2001503081A JP2001503081A JP10514343A JP51434398A JP2001503081A JP 2001503081 A JP2001503081 A JP 2001503081A JP 10514343 A JP10514343 A JP 10514343A JP 51434398 A JP51434398 A JP 51434398A JP 2001503081 A JP2001503081 A JP 2001503081A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- anhydride
- acid
- additive
- fuels
- 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.)
- Granted
Links
- 239000000654 additive Substances 0.000 title claims abstract description 58
- 239000000446 fuel Substances 0.000 title claims abstract description 29
- 238000004140 cleaning Methods 0.000 title claims abstract description 19
- 238000005260 corrosion Methods 0.000 title claims abstract description 18
- 230000007797 corrosion Effects 0.000 title claims abstract description 18
- 239000000203 mixture Substances 0.000 title claims description 20
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- 229920000768 polyamine Polymers 0.000 claims abstract description 19
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- -1 monocarboxylic acid compound Chemical class 0.000 claims abstract description 13
- 239000002253 acid Substances 0.000 claims abstract description 11
- 229940126062 Compound A Drugs 0.000 claims abstract description 9
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000001408 amides Chemical class 0.000 claims abstract description 6
- 150000003949 imides Chemical group 0.000 claims abstract description 6
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 claims abstract description 5
- 230000000996 additive effect Effects 0.000 claims description 29
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 15
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 13
- 229940014800 succinic anhydride Drugs 0.000 claims description 13
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 238000009833 condensation Methods 0.000 claims description 7
- 230000005494 condensation Effects 0.000 claims description 7
- 239000003599 detergent Substances 0.000 claims description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- 238000004821 distillation Methods 0.000 claims description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 4
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 235000011044 succinic acid Nutrition 0.000 claims description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 3
- WVRNUXJQQFPNMN-VAWYXSNFSA-N 3-[(e)-dodec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCC\C=C\C1CC(=O)OC1=O WVRNUXJQQFPNMN-VAWYXSNFSA-N 0.000 claims description 3
- KAYAKFYASWYOEB-ISLYRVAYSA-N 3-[(e)-octadec-1-enyl]oxolane-2,5-dione Chemical group CCCCCCCCCCCCCCCC\C=C\C1CC(=O)OC1=O KAYAKFYASWYOEB-ISLYRVAYSA-N 0.000 claims description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 claims description 3
- 150000003444 succinic acids Chemical class 0.000 claims description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 2
- 239000001361 adipic acid Substances 0.000 claims description 2
- 235000011037 adipic acid Nutrition 0.000 claims description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 2
- 239000010779 crude oil Substances 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 235000011087 fumaric acid Nutrition 0.000 claims description 2
- 239000001630 malic acid Substances 0.000 claims description 2
- 235000011090 malic acid Nutrition 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 239000000080 wetting agent Substances 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 10
- 238000002156 mixing Methods 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000002283 diesel fuel Substances 0.000 description 9
- 230000001588 bifunctional effect Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 3
- 230000035876 healing Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- RCBGGJURENJHKV-UHFFFAOYSA-N 2-methylhept-1-ene Chemical compound CCCCCC(C)=C RCBGGJURENJHKV-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical group NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- KPADFPAILITQBG-UHFFFAOYSA-N non-4-ene Chemical compound CCCCC=CCCC KPADFPAILITQBG-UHFFFAOYSA-N 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000004711 α-olefin Substances 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
- C10L1/22—Organic compounds containing nitrogen
-
- 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
- C10L1/22—Organic compounds containing nitrogen
- C10L1/221—Organic compounds containing nitrogen compounds of uncertain formula; reaction products where mixtures of compounds are obtained
-
- 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)
-
- 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
-
- 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
- C10L10/18—Use of additives to fuels or fires for particular purposes use of detergents or dispersants for purposes not provided for in groups C10L10/02 - C10L10/16
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)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Lubricants (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.第一級ポリアミンよりなる化合物Cと少なくとも1つのポリアルケニルジカ ルボン酸または無水物化合物よりなる化合物Aおよび少なくとも1つの直鎖また は分岐鎖モノカルボン酸または無水物化合物よりなる化合物Bとの縮合から得ら れるアミドもしくはイミド官能基を含むエンジン燃料、特にディーゼルタイプの 燃料用の洗浄および耐食性添加剤であって、直鎖または分岐鎖アルケニル基当た り2ないし20個の炭素原子を含み、200ないし3,000で変化する平均分 子量を有する60ないし90重量%の化合物A、鎖当たり2ないし6個の炭素原 子を含む0.1ないし10重量%の化合物B、および以下の一般式(I): H2N−[−(CHR1−(CH2)p−CHR2)n−NH]m−H (I) [式中、同一または異なるR1およびR2は、水素または1ないし4個の炭素原子 を含む炭化水素基を表し、nは1ないし3で変化する整数、mは1ないし10で 変化する整数、およびpは0または1に等しい整数である] の10ないし30%の化合物を混合することによって得られ、 A、BおよびCは1/(0.1ないし1)/(1ないし3)に対応するA/B/ Cモル比で使用され、A/B/Cは決して1/1/1ではない特徴とする該添加 剤。 2.ポリアルケニルカルボン酸化合物Aの平均分子量が200ないし2,000 、好ましくは200ないし1,500で変化することを特徴とする請求項1記載 の添加剤。 3.C/Aモル比が1.3ないし2.0で変化し、B/Aモル比が0.1ないし 0.8であることを特徴とする請求項1または2記載の添加剤。 4.ポリアルケニルカルボン酸化合物が、化合物1グラム当たり水酸化カリウム の0.5ないし1.2ミリ等量で変化する無水物数を持つポリアルケニルコハク 酸および無水物誘導体から選択されることを特徴とする請求項1ないし3いずれ か1項記載の添加剤。 5.該コハタ酸無水物がn−オクタデセニルコハク酸無水物、ドデセニルコハク 酸無水物およびポリイソブテニルコハク酸無水物および200ないし1,500 で変化する重量平均分子量を持ついずれかのコハク酸無水物よりなる群から選択 されることを特徴とする請求項1ないし4いずれか1項記載の添加剤。 6.化合物Bがメタクリル酸、アタリル酸、マレイン酸無水物、コハク酸無水物 、リンゴ酸、フマル酸およびアジピン酸よりなる群から選択されることを特徴と する請求項1ないし5いずれか1項記載の濡加剤。 7.第一級ポリアミンがジエチレントリアミン、ジプロピレントリアミン、トリ エチレンテトラミン、テトラエチレンペンタミンおよびそれらの置換誘導体より なる群から選択されるポリアミンである請求項1ないし6記載の添加剤。 8.i)65および250℃の間の沸点を持つ有機溶剤に生成物AおよびBを導 入し、 ii)生成物Cを徐々に導入し、 iii)次いで、混合物の温度を65および250℃、好ましくは80および 200℃の間の温度まで上昇させ、 iv)最後に、水/溶剤ヘテロ共沸物またはヘテロ共沸物類を蒸留し、ここで 、該混合物は、該ポリアミンと該酸との縮合によって形成された水が完全に除去 されるまで、0.5時間ないし7時間、好ましくは1ないし5時間、ヘテロ共沸 物またはヘテロ共沸物類の蒸留温度に還流下で維持される工程の順序によって得 られることを特徴とする請求項1ないし7いずれか1 項記載の添加剤。 9.主として、150および400℃の間の粗製油直接蒸留留分から得られる少 なくとも1つの中間蒸留物または30に等しいかそれより高いセタン価を持つ他 の燃料を含み、かつ請求項1ないし8いずれか1項記載の少なくとも1つの添加 剤を少量含む燃料。 10.少なくとも50ppm、好ましくは60ないし600ppmの洗浄および 耐食性添加剤または添加剤類を含有することを特徴とする請求項9記載の燃料。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR96/11388 | 1996-09-18 | ||
FR9611388A FR2753455B1 (fr) | 1996-09-18 | 1996-09-18 | Additif detergent et anti-corrosion pour carburants et composition de carburants |
PCT/FR1997/001634 WO1998012283A1 (fr) | 1996-09-18 | 1997-09-17 | Additif detergent et anti-corrosion pour carburants et composition de carburants |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2001503081A true JP2001503081A (ja) | 2001-03-06 |
JP3763584B2 JP3763584B2 (ja) | 2006-04-05 |
Family
ID=9495858
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51434398A Expired - Fee Related JP3763584B2 (ja) | 1996-09-18 | 1997-09-17 | 燃料および燃料組成物用の洗浄および耐食性添加剤 |
Country Status (16)
Country | Link |
---|---|
US (1) | US6083287A (ja) |
EP (1) | EP0938535B1 (ja) |
JP (1) | JP3763584B2 (ja) |
KR (1) | KR100467280B1 (ja) |
AT (1) | ATE214085T1 (ja) |
BR (1) | BR9713201A (ja) |
CA (1) | CA2266522C (ja) |
DE (1) | DE69710913T2 (ja) |
DK (1) | DK0938535T3 (ja) |
ES (1) | ES2170386T3 (ja) |
FR (1) | FR2753455B1 (ja) |
HU (1) | HU223377B1 (ja) |
MY (1) | MY116976A (ja) |
PT (1) | PT938535E (ja) |
RU (1) | RU2165448C2 (ja) |
WO (1) | WO1998012283A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU594723B2 (en) * | 1985-12-19 | 1990-03-15 | Minnesota Mining And Manufacturing Company | Method and apparatus for making optical devices |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050268536A1 (en) * | 2004-06-02 | 2005-12-08 | Polar Molecular Corporation | Diesel motor fuel additive composition |
US20070283618A1 (en) * | 2006-06-09 | 2007-12-13 | Malfer Dennis J | Diesel detergents |
EP1967568A1 (de) * | 2007-02-28 | 2008-09-10 | Basf Se | Polyisobutylbernsteinsäureanhydridderivate als Korrosionsinhibitoren in Kraftstoffen |
GB0714725D0 (en) * | 2007-07-28 | 2007-09-05 | Innospec Ltd | Fuel oil compositions and additives therefor |
FR2925909B1 (fr) * | 2007-12-26 | 2010-09-17 | Total France | Additifs bifonctionnels pour hydrocarbures liquides obtenus par greffage a partir de copolymeres d'ethylene et/ou de propylene et d'esters vinyliques |
FR2925916B1 (fr) * | 2007-12-28 | 2010-11-12 | Total France | Terpolymere ethylene/acetate de vinyle/esters insatures comme additif ameliorant la tenue a froid des hydrocarbures liquides comme les distillats moyens et les carburants ou combustibles |
FR2940314B1 (fr) | 2008-12-23 | 2011-11-18 | Total Raffinage Marketing | Carburant de type gazole pour moteur diesel a fortes teneurs en carbone d'origine renouvelable et en oxygene |
FR2943678B1 (fr) | 2009-03-25 | 2011-06-03 | Total Raffinage Marketing | Polymeres (meth)acryliques de bas poids moleculaire, exempts de composes soufres,metalliques et halogenes et de taux de monomeres residuels faible,leur procede de preparation et leurs utilisations |
FR2947558B1 (fr) | 2009-07-03 | 2011-08-19 | Total Raffinage Marketing | Terpolymere et ethylene/acetate de vinyle/esters insatures comme additif ameliorant la tenue a froid des hydrocarbures liquides comme les distillats moyens et les carburants ou combustibles |
US8668749B2 (en) | 2010-11-03 | 2014-03-11 | Afton Chemical Corporation | Diesel fuel additive |
FR2969620B1 (fr) | 2010-12-23 | 2013-01-11 | Total Raffinage Marketing | Resines alkylphenol-aldehyde modifiees, leur utilisation comme additifs ameliorant les proprietes a froid de carburants et combustibles hydrocarbones liquides |
FR2971254B1 (fr) | 2011-02-08 | 2014-05-30 | Total Raffinage Marketing | Compositions liquides pour marquer les carburants et combustibles hydrocarbones liquides, carburants et combustibles les contenant et procede de detection des marqueurs |
FR2987052B1 (fr) | 2012-02-17 | 2014-09-12 | Total Raffinage Marketing | Additifs ameliorant la resistance a l'usure et au lacquering de carburants de type gazole ou biogazole |
FR2991992B1 (fr) | 2012-06-19 | 2015-07-03 | Total Raffinage Marketing | Compositions d'additifs et leur utilisation pour ameliorer les proprietes a froid de carburants et combustibles |
FR2994695B1 (fr) | 2012-08-22 | 2015-10-16 | Total Raffinage Marketing | Additifs ameliorant la resistance a l'usure et au lacquering de carburants de type gazole ou biogazole |
FR3000102B1 (fr) | 2012-12-21 | 2015-04-10 | Total Raffinage Marketing | Utilisation d'un compose viscosifiant pour ameliorer la stabilite au stockage d'un carburant ou combustible hydrocarbone liquide |
FR3000101B1 (fr) | 2012-12-21 | 2016-04-01 | Total Raffinage Marketing | Composition gelifiee de carburant ou combustible hydrocarbone et procede de preparation d'une telle composition |
FR3005061B1 (fr) | 2013-04-25 | 2016-05-06 | Total Raffinage Marketing | Additif pour ameliorer la stabilite a l'oxydation et/ou au stockage de carburants ou combustibles hydrocarbones liquides |
RU2539307C1 (ru) * | 2013-06-07 | 2015-01-20 | Государственное научное учреждение Всероссийский научно-исследовательский институт механизации сельского хозяйства Российской академии сельскохозяйственных наук (ГНУ ВИМ Россельхозакадемии) | Способ снижения нагарообразования в двигателе, работающем на топливе из растительного масла |
FR3021663B1 (fr) | 2014-05-28 | 2016-07-01 | Total Marketing Services | Composition gelifiee de carburant ou combustible hydrocarbone liquide et procede de preparation d'une telle composition |
EP3056526A1 (fr) | 2015-02-11 | 2016-08-17 | Total Marketing Services | Copolymeres a blocs et leur utilisation pour ameliorer les proprietes a froid de carburants ou combustibles |
EP3056527A1 (fr) | 2015-02-11 | 2016-08-17 | Total Marketing Services | Copolymeres a blocs et leur utilisation pour ameliorer les proprietes a froid de carburants ou combustibles |
EP3144059A1 (en) | 2015-09-16 | 2017-03-22 | Total Marketing Services | Method for preparing microcapsules by double emulsion |
FR3054240B1 (fr) | 2016-07-21 | 2018-08-17 | Total Marketing Services | Utilisation de copolymeres pour ameliorer les proprietes a froid de carburants ou combustibles |
FR3055135B1 (fr) | 2016-08-18 | 2020-01-10 | Total Marketing Services | Procede de fabrication d'un additif de lubrifiance pour carburant a faible teneur en soufre. |
FR3075813B1 (fr) | 2017-12-21 | 2021-06-18 | Total Marketing Services | Utilisation de polymeres reticules pour ameliorer les proprietes a froid de carburants ou combustibles |
FR3081879B1 (fr) | 2018-05-29 | 2020-11-13 | Total Marketing Services | Composition de carburant et procede de fonctionnement d’un moteur a combustion interne |
FR3085384B1 (fr) | 2018-08-28 | 2021-05-28 | Total Marketing Services | Utilisation de copolymeres specifiques pour ameliorer les proprietes a froid de carburants ou combustibles |
FR3085383B1 (fr) | 2018-08-28 | 2020-07-31 | Total Marketing Services | Composition d'additifs comprenant au moins un copolymere, un additif fluidifiant a froid et un additif anti-sedimentation |
FR3091539B1 (fr) | 2019-01-04 | 2021-10-01 | Total Marketing Services | Utilisation de copolymères spécifiques pour abaisser la température limite de filtrabilité de carburants ou combustibles |
FR3101882B1 (fr) | 2019-10-14 | 2022-03-18 | Total Marketing Services | Utilisation de polymères cationiques particuliers comme additifs pour carburants et combustibles |
FR3103812B1 (fr) | 2019-11-29 | 2023-04-07 | Total Marketing Services | Utilisation de composés alkyl phénol comme additifs de détergence |
FR3103815B1 (fr) | 2019-11-29 | 2021-12-17 | Total Marketing Services | Utilisation de diols comme additifs de détergence |
FR3113063B1 (fr) | 2020-07-31 | 2022-08-12 | Total Marketing Services | Utilisation de copolymères à distribution de masse molaire spécifique pour abaisser la température limite de filtrabilité de carburants ou de combustibles |
FR3125298A1 (fr) | 2021-07-19 | 2023-01-20 | Totalenergies Marketing Services | Utilisation d’une composition d’additifs pour réduire les émissions des véhicules Diesel |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB684640A (en) * | 1949-11-14 | 1952-12-24 | Socony Vacuum Oil Co Inc | Reaction products of n-acylated polyalkylenepolyamines with alkenyl succinic acids or anhydrides or derivatives thereof |
NL296869A (ja) * | 1962-09-04 | |||
US3185704A (en) * | 1962-09-04 | 1965-05-25 | Exxon Research Engineering Co | Formamide of mono-alkenyl succinimide |
US3216936A (en) * | 1964-03-02 | 1965-11-09 | Lubrizol Corp | Process of preparing lubricant additives |
US3445386A (en) * | 1967-01-13 | 1969-05-20 | Mobil Oil Corp | Detergent compositions |
FR2044305A5 (en) * | 1969-05-14 | 1971-02-19 | Inst Francais Du Petrole | Nitrogen contng comps useful as fuel additivs |
US3630902A (en) * | 1969-07-23 | 1971-12-28 | Chevron Res | Lubricant additives derived from catalytically polymerized reaction products of succinimides and unsaturated monocarboxylic acids or anhydrides |
US3652616A (en) * | 1969-08-14 | 1972-03-28 | Standard Oil Co | Additives for fuels and lubricants |
US4501597A (en) * | 1984-07-02 | 1985-02-26 | Texaco Inc. | Detergent fuel composition containing alkenylsuccinimide oxamides |
US4780111A (en) * | 1985-11-08 | 1988-10-25 | The Lubrizol Corporation | Fuel compositions |
US5034018A (en) * | 1987-11-30 | 1991-07-23 | Exxon Chemical Patents Inc. | Fuel additives derived from amido-amines (PT-731) |
US5171421A (en) * | 1991-09-09 | 1992-12-15 | Betz Laboratories, Inc. | Method for controlling fouling deposit formation in a liquid hydrocarbonaceous medium |
-
1996
- 1996-09-18 FR FR9611388A patent/FR2753455B1/fr not_active Expired - Fee Related
-
1997
- 1997-09-17 CA CA002266522A patent/CA2266522C/fr not_active Expired - Fee Related
- 1997-09-17 WO PCT/FR1997/001634 patent/WO1998012283A1/fr not_active Application Discontinuation
- 1997-09-17 DE DE69710913T patent/DE69710913T2/de not_active Expired - Lifetime
- 1997-09-17 RU RU99107667/04A patent/RU2165448C2/ru not_active IP Right Cessation
- 1997-09-17 DK DK97919109T patent/DK0938535T3/da active
- 1997-09-17 EP EP97919109A patent/EP0938535B1/fr not_active Expired - Lifetime
- 1997-09-17 BR BR9713201-2A patent/BR9713201A/pt not_active IP Right Cessation
- 1997-09-17 ES ES97919109T patent/ES2170386T3/es not_active Expired - Lifetime
- 1997-09-17 US US09/147,623 patent/US6083287A/en not_active Expired - Lifetime
- 1997-09-17 JP JP51434398A patent/JP3763584B2/ja not_active Expired - Fee Related
- 1997-09-17 KR KR10-1999-7002270A patent/KR100467280B1/ko not_active IP Right Cessation
- 1997-09-17 HU HU9903777A patent/HU223377B1/hu not_active IP Right Cessation
- 1997-09-17 PT PT97919109T patent/PT938535E/pt unknown
- 1997-09-17 AT AT97919109T patent/ATE214085T1/de active
- 1997-09-18 MY MYPI97004342A patent/MY116976A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU594723B2 (en) * | 1985-12-19 | 1990-03-15 | Minnesota Mining And Manufacturing Company | Method and apparatus for making optical devices |
Also Published As
Publication number | Publication date |
---|---|
BR9713201A (pt) | 2000-04-04 |
EP0938535A1 (fr) | 1999-09-01 |
EP0938535B1 (fr) | 2002-03-06 |
PT938535E (pt) | 2002-08-30 |
DK0938535T3 (da) | 2002-06-24 |
FR2753455A1 (fr) | 1998-03-20 |
DE69710913D1 (de) | 2002-04-11 |
HUP9903777A2 (hu) | 2000-04-28 |
HU223377B1 (hu) | 2004-06-28 |
US6083287A (en) | 2000-07-04 |
CA2266522C (fr) | 2005-07-26 |
ATE214085T1 (de) | 2002-03-15 |
DE69710913T2 (de) | 2002-10-31 |
MY116976A (en) | 2004-04-30 |
ES2170386T3 (es) | 2002-08-01 |
FR2753455B1 (fr) | 1998-12-24 |
RU2165448C2 (ru) | 2001-04-20 |
WO1998012283A1 (fr) | 1998-03-26 |
CA2266522A1 (fr) | 1998-03-26 |
HUP9903777A3 (en) | 2001-10-29 |
JP3763584B2 (ja) | 2006-04-05 |
KR20000036209A (ko) | 2000-06-26 |
KR100467280B1 (ko) | 2005-01-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3763584B2 (ja) | 燃料および燃料組成物用の洗浄および耐食性添加剤 | |
KR100284207B1 (ko) | 연료첨가제, 이들의 제조방법 및 이들 첨가제를 함유하는 가솔린 엔진 연료 | |
KR100663774B1 (ko) | 연료 조성물 | |
US3443918A (en) | Gasoline composition | |
EP0557516B1 (en) | Fuel additive compositions containing polyisobutenyl succinimides | |
US6156082A (en) | Fuel additives | |
AU2004227095B2 (en) | Fuel composition | |
EP0526129B1 (en) | Compositions for control of octane requirement increase | |
JP2005520018A (ja) | ガソリン添加物 | |
US20080141580A1 (en) | Fuel Oil Compositions | |
WO1990010051A1 (en) | Fuel composition for control of intake valve deposits | |
US4581040A (en) | Polyoxyisopropylenediamine-acid anhydride-polyamine reaction product and motor fuel composition containing same | |
US5752990A (en) | Composition and method for reducing combustion chamber deposits, intake valve deposits or both in spark ignition internal combustion engines | |
US6488723B2 (en) | Motor fuel additive composition and method for preparation thereof | |
US4976746A (en) | Formulations of nitrogenated additives for engine fuels and the engine fuels containing them | |
EP0441014B1 (en) | Compositions for control of induction system deposits | |
JPH05194965A (ja) | エステル官能基を有する物質と洗浄剤−分散剤とを含む燃料用添加剤調合物 | |
US4997456A (en) | Fuel compositions | |
JPS6136040B2 (ja) | ||
US20040048765A1 (en) | Composition | |
JP3561765B2 (ja) | 少なくともアルコキシル化イミダゾ・オキサゾール化合物を含む発動機燃料用の添加剤配合物 | |
EP1947161A1 (en) | Fuel oil compositions | |
WO2006098741A2 (en) | Motor fuel additive composition | |
CA2613953A1 (en) | Fuel oil compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20040615 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20040908 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20041025 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20041027 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20050726 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20051025 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20051220 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20060117 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20090127 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20100127 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110127 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110127 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120127 Year of fee payment: 6 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130127 Year of fee payment: 7 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |