NO750823L - - Google Patents
Info
- Publication number
- NO750823L NO750823L NO750823A NO750823A NO750823L NO 750823 L NO750823 L NO 750823L NO 750823 A NO750823 A NO 750823A NO 750823 A NO750823 A NO 750823A NO 750823 L NO750823 L NO 750823L
- Authority
- NO
- Norway
- Prior art keywords
- ester
- acid
- fatty acid
- esters
- alcohol
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 claims description 21
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 17
- 229930195729 fatty acid Natural products 0.000 claims description 17
- 239000000194 fatty acid Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 12
- 238000002485 combustion reaction Methods 0.000 claims description 11
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000007859 condensation product Substances 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000005313 fatty acid group Chemical group 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 235000010446 mineral oil Nutrition 0.000 claims description 4
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 claims description 4
- 239000002816 fuel additive Substances 0.000 claims description 3
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000000654 additive Substances 0.000 description 14
- -1 fatty acid esters Chemical class 0.000 description 13
- 239000000446 fuel Substances 0.000 description 10
- 230000000996 additive effect Effects 0.000 description 9
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 125000003158 alcohol group Chemical group 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- MMXKVMNBHPAILY-UHFFFAOYSA-N ethyl laurate Chemical compound CCCCCCCCCCCC(=O)OCC MMXKVMNBHPAILY-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- ZQWPRMPSCMSAJU-UHFFFAOYSA-N methyl cyclohexanecarboxylate Chemical compound COC(=O)C1CCCCC1 ZQWPRMPSCMSAJU-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- RMZNXRYIFGTWPF-UHFFFAOYSA-N 2-nitrosoacetic acid Chemical compound OC(=O)CN=O RMZNXRYIFGTWPF-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
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- 239000001293 FEMA 3089 Substances 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- IPTNXMGXEGQYSY-UHFFFAOYSA-N acetic acid;1-methoxybutan-1-ol Chemical compound CC(O)=O.CCCC(O)OC IPTNXMGXEGQYSY-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- LSCGCDXAEHGNMD-UHFFFAOYSA-N calcium;phenyl octadecanoate Chemical compound [Ca].CCCCCCCCCCCCCCCCCC(=O)OC1=CC=CC=C1 LSCGCDXAEHGNMD-UHFFFAOYSA-N 0.000 description 1
- 239000010624 camphor oil Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- JLEKJZUYWFJPMB-UHFFFAOYSA-N ethyl 2-methoxyacetate Chemical compound CCOC(=O)COC JLEKJZUYWFJPMB-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- WUKXMJCZWYUIRZ-UHFFFAOYSA-N hexadecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(C)O WUKXMJCZWYUIRZ-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- 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
- 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
- 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
-
- 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
- C10L10/02—Use of additives to fuels or fires for particular purposes for reducing smoke development
-
- 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
-
- 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
- C10L1/16—Hydrocarbons
- C10L1/1616—Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
-
- 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
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
- C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Description
Ved drift av forbrenningsmotorer oppstår det ved During the operation of internal combustion engines, there is
mange driftstilstander som følge av ufullstendig forbrenning mangler som: Korrosjon og slitasje på grunn av sure forbrennings-produkter; many operating conditions resulting from incomplete combustion are missing such as: Corrosion and wear due to acidic combustion products;
rester i brennkammeret og i utslippsveiene; residues in the combustion chamber and in the discharge paths;
skadelige stoffer som CO og uforbrente hydrokarboner i avgassene. harmful substances such as CO and unburned hydrocarbons in the exhaust gases.
Disse uungåelige fenomener er spesielt alvorlige ved'motorer som kjører i underkjølt tilstand3slik dette er tilfelle over korte strekninger. These unavoidable phenomena are particularly serious in the case of engines running in a subcooled state3, as is the case over short distances.
I tillegg til de nevnte mangler slik de oppstår på grunn av ufullstendig . forbrenning, kommer det ved forgassermot-orer forsmussing utenifra i innsugningssystemet og gjennom veiv-husluftningen. Disse forurensninger kan i sterk grad forstyrre dannelsen av en riktig drivstoffblanding, noe som fører til en forsterkning av de ovenfor angitte mangler. Fremfor alt kan inn-holdet av giftige CO i avgassene stige over den tillatte verdi. In addition to the aforementioned deficiencies as they arise due to incompleteness. combustion, in the case of carbureted engines, contamination comes from the outside in the intake system and through the crankcase ventilation. These contaminants can greatly interfere with the formation of a proper fuel mixture, leading to an amplification of the above-mentioned deficiencies. Above all, the content of toxic CO in the exhaust gases can rise above the permitted value.
Man forsøker å tilsidesette de ovenfor angitte mangler ved tilsetning av forskjellige tilsetningsstoffer til driv-stoffene. Et slikt tilsetningsstoff renser innsugningssystemet kontinuerlig for ikke eller tungt fordampende forurensninger slik som gummi, harpikser, smøremiddelande ler, skitt og ligenende, og • sikrer således dannelsen av en riktig drivstoffblanding. Like-ledes oppløses forbrenningsrester i brennkammeret og i utslippsveiene og beskytter materialene.for korrosjon. Attempts are made to override the above-mentioned shortcomings by adding various additives to the propellants. Such an additive continuously cleans the intake system of non- or heavily evaporating contaminants such as rubber, resins, lubricant clay, dirt and the like, and • thus ensures the formation of a correct fuel mixture. In the same way, combustion residues dissolve in the combustion chamber and in the discharge paths and protect the materials from corrosion.
Man har fastslått at tilsetning av et slikt tilsetningsstoff gir følgende fordeler: Beskyttelse av materialene for korrosjon; It has been established that the addition of such an additive provides the following advantages: Protection of the materials from corrosion;
anvendelsesmuligheter for drivstoffer med lavere application possibilities for fuels with lower
oktantall i Ottomotorer; octane number in Otto engines;
riktig dannelse av drivstoffblanding ved renhold av innsugningssystemet; correct formation of fuel mixture when cleaning the intake system;
reduksjon av skadelige stoffer i avgassene, slik som CO og uforbrente hydrokarboner; reduction of harmful substances in the exhaust gases, such as CO and unburned hydrocarbons;
renhold av brennkammeret og utslippsveiene for for-ta rennings rester; cleaning of the combustion chamber and the discharge paths to remove runoff residues;
forbedring av forbrenningen ved motordrivstoffer. improvement of the combustion of motor fuels.
Som tils-oningsstoffer er det allerede foreslått tall-rike kombinasjoner av antikorrosivt og rensende virkende sub-stanser. Det dreier seg derved hovédsakelig om kombinasjoner av korrosjohsbeskyttelsesmidler og også utvalgte detergentier med oppløsningsmidler slik som terpentinolj er, kamferoljer, alkoholr er, ketoner, estere og halogenhydrokarboner. I den senere tid er det som spesielt virksomt middel foreslått et additiv bestående av polyalkoholfettsyreestere, dvs. frie fettsyrer med minst 12 C-atomer, alifatiske fettsyrer slik som kalsiumfenylstearat. Videre er det foreslått i dette additiv i stedet for alifatiske fettsyreestere å anvende estere av fenol og dennes homologer eller fettsyreestere med en hydroksy- eller alkoksygruppe i fettsyredelen eller i alkoholdelen eller i begge, samt blandinger av disse estere. Numerous combinations of anticorrosive and purifying active substances have already been proposed as additives. This mainly involves combinations of corrosion protection agents and also selected detergents with solvents such as turpentine oil, camphor oils, alcohols, ketones, esters and halogenated hydrocarbons. In recent times, an additive consisting of polyalcohol fatty acid esters, i.e. free fatty acids with at least 12 C atoms, aliphatic fatty acids such as calcium phenylstearate, has been proposed as a particularly effective agent. Furthermore, it is proposed in this additive instead of aliphatic fatty acid esters to use esters of phenol and its homologues or fatty acid esters with a hydroxy or alkoxy group in the fatty acid part or in the alcohol part or in both, as well as mixtures of these esters.
Drivmiddeltilsetningsstoffene ifølge oppfinnelsen erkarakterisert vedat de som bærerkomponent inneholder minst en primær eller sekundær enverdig alkohol og/eller ketoalkohol. The fuel additives according to the invention are characterized in that they contain at least one primary or secondary monohydric alcohol and/or keto alcohol as a carrier component.
Et spesielt foretrukket tilsetningsmiddel for drivstoffer ifølge oppfinnelsen inneholder A particularly preferred additive for fuels according to the invention contains
a) et basisk kondensasjonsprodukt av 1 mol av et poly-etanolamin og minst 1 og maksimalt 2 mol av en fettsyre med minst a) a basic condensation product of 1 mol of a polyethanolamine and at least 1 and at most 2 mol of a fatty acid with at least
10 karbonatomer eller en ekvivalent mengde av en blanding av slike fettsyrer, b) en ester som ikke inneholder basiske grupper, hvilken ester stammer fra en eventuelt med hydroksy- eller alkoksygrupper substituert fettsyre, en aromatisk eller hydroaromatisk syre henholdsvis naftensyre eller en blanding av slike estere, hvilke estere ikke inneholder basiske -grupper, c) en eller flere mineraloljeraffinater med en viskosi-tet på minst 1,6° E/20°C og maksimalt 15° E/50°C og d) som bærerkomponent minst en primær eller sekundær en- 10 carbon atoms or an equivalent amount of a mixture of such fatty acids, b) an ester that does not contain basic groups, which ester originates from a fatty acid optionally substituted with hydroxy or alkoxy groups, an aromatic or hydroaromatic acid or naphthenic acid or a mixture of such esters , which esters do not contain basic groups, c) one or more mineral oil raffinates with a viscosity of at least 1.6° E/20°C and a maximum of 15° E/50°C and d) as carrier component at least one primary or secondary one-
verdig alkohol og/eller ketoalkohol. worthy alcohol and/or keto alcohol.
Som bærerkomponent foretrekkes primære eller sekundære enverdige alkoholer med opptil 10 karbonatomer, spesielt opptil 5 karbonatomer, slik som f.eks. propanoler og butanoler, spesielt isobutanol, men også metanol, isooktanol, Isononanol, dekanol osv., samt de primære eller sekundære enverdige keto-alkoholer, spesielt diacetonalkohol. °E betyr °Engler. Komponentene a) og b) anvendes vanligvis i mengder på opptil 50 vekt-% komponenten c) oftest i mengder fra 10 til 15%, ved tilsetningsstoffer for dieseldrivstoffer også i mengder opptil 80%. Bærerkomponenten utgjør vanligvis ca. 50% av tilsteningsstoffet, kan imidlertid også foreligge i mengder opptil ca. 80$. Primary or secondary monohydric alcohols with up to 10 carbon atoms, especially up to 5 carbon atoms, such as e.g. propanols and butanols, especially isobutanol, but also methanol, isooctanol, isononanol, decanol, etc., as well as the primary or secondary monovalent keto alcohols, especially diacetone alcohol. °E means °Angels. Components a) and b) are usually used in amounts of up to 50% by weight, component c) most often in amounts from 10 to 15%, with additives for diesel fuels also in amounts up to 80%. The carrier component usually amounts to approx. 50% of the calcifying substance, however, can also be present in amounts of up to approx. 80$.
Til fremstilling av komponenten a) kan man på i og for seg kjent måte oppvarme f. eks. 1 mol trietanolamin med 1-. mol av en fettsyre med minst 10 karbonatomer, f.eks. oljesyre, i en til tre timer til temperaturer på over 130°C. For å oppnå lyse kondensasjonsprodukter er det fordelaktig å gjennomføre reaksjonen i beholdere av glass, porselen eller korrosjonsfaste stål, det kan også være av.nytte å gjennomføre reaksjonen i vakuum under tilsetning av metalldesaktivatorer, slik som f.eks. en Schiff'sk base av salicylaldehyd. Etter fullstendig avdestilla-sjon av vann og avkjøling oppnår man ved anvendelse av oljesyre et lysegult til lett brunlig farget kondensasjonsprodukt som be-står overveiende av monooljesyreestren av trietanolamin. Hvis man i stedet for 1 mol oljesyre 2 mol av denne syre oppstår overveiende trietanolamindioljesyreester. De to nevnte kondensasjonsprodukter er lett oppløselige i de fleste oppløsningsmidler og i de mineraloljeraffinater som skal anvendes. For the production of component a), one can heat up in a manner known per se, e.g. 1 mole of triethanolamine with 1-. moles of a fatty acid with at least 10 carbon atoms, e.g. oleic acid, for one to three hours to temperatures above 130°C. In order to obtain bright condensation products, it is advantageous to carry out the reaction in containers made of glass, porcelain or corrosion-resistant steel, it can also be useful to carry out the reaction in a vacuum with the addition of metal deactivators, such as e.g. a Schiff's base of salicylaldehyde. After complete distillation of water and cooling, a pale yellow to slightly brownish colored condensation product is obtained by using oleic acid, which consists predominantly of the monooleic acid ester of triethanolamine. If, instead of 1 mol of oleic acid, 2 mol of this acid is used, predominantly triethanolamine diol ester is produced. The two condensation products mentioned are easily soluble in most solvents and in the mineral oil raffinates to be used.
I stedet for kondensasjonsproduktet av trietanolamin og en fettsyre med minst 10 karbonatomer kan man også anvende et produkt som oppnås ved analogkondensasjon av 1 mol dietanolamin med 1 mol av en fettsyre med minst 10 karbonatomer 'henholdsvis en blanding av slike fettsyrer. Hvis man som fettsyre anvender teknisk oljesyre oppnår man som reaksjonsprodukt overveiene monooljesyreestren av dietanolamin. Instead of the condensation product of triethanolamine and a fatty acid with at least 10 carbon atoms, a product obtained by analog condensation of 1 mol of diethanolamine with 1 mol of a fatty acid with at least 10 carbon atoms can also be used, respectively a mixture of such fatty acids. If technical oleic acid is used as the fatty acid, the reaction product is predominantly the monooleic acid ester of diethanolamine.
Som esterkomponenten b) egner seg spesielt alle til-svarende og i hydrokarboner oppløselige høyere kokende estere eller en blanding av estere, fortrinnsvis imidlertid slike med en begynnende koking på over 150°C, slik som f.eks. laurinsyre-etylester, smørsyreisooctylester3eddiksyreoleylester3 benzo-syreetylester3naftenisopropylester og cykloheksankarbonsyre-metylester. As the ester component b), all corresponding and hydrocarbon-soluble higher-boiling esters or a mixture of esters are particularly suitable, preferably, however, those with an initial boiling of over 150°C, such as e.g. lauric acid ethyl ester, butyric acid isooctyl ester 3 acetic oleyl ester 3 benzoic acid ethyl ester 3 naphthenic isopropyl ester and cyclohexanecarboxylic acid methyl ester.
Som ester komponent b) har dog estere av fenol og As ester component b) however has esters of phenol and
sine homologer og fettsyreestre der enten alkoholdelen eller fettsyredelen eller begge disse bærer en hydroksy- eller alkoksygruppe, eller blanding av slike' estre, vist seg spesielt virk-somme. Som estre av ^enol og dennes homologer skal f.eks. nevnes kresylacetat3xylenacetat, fenylnaftenat, kresylnaftenat eller kresylester av cykloheksankarbonsyre. Fettsyreestre som bærer en hydroksy- eller alkoksygruppe er f.eks. metoksybutylacetat, metoksyeddiksyreetylester,metoksybutylestren av metoksyeddik-syre, melkesyrecetylester3laurinsyremonoester av metylglykol, glykonmonooleat eller' blandinger derav. their homologues and fatty acid esters where either the alcohol part or the fatty acid part or both of these carry a hydroxy or alkoxy group, or mixtures of such esters, have proven particularly effective. As esters of ^enol and its homologues, e.g. mention is made of cresyl acetate-xylene acetate, phenyl naphthenate, cresyl naphthenate or cresyl ester of cyclohexanecarboxylic acid. Fatty acid esters bearing a hydroxy or alkoxy group are e.g. methoxybutyl acetate, methoxyacetic acid ethyl ester, methoxybutyl ester of methoxyacetic acid, lactic acid cetyl ester 3 lauric acid monoester of methyl glycol, glycone monooleate or' mixtures thereof.
Man kan oppløse komponentene a) og b) i vilkårlig rekkefølge i komponenten c), bærerkomponenten kan tilsettes på Components a) and b) can be dissolved in any order in component c), the carrier component can be added on
et hvilken som helst tidspunkt. any time.
Ved motorførsøk har det vist seg at allerede små mengder av de enkelte bestanddeler i tilsetningsstoffet utøver en optimal virkning på et vanlig dri-vstoff. Vanligvis er det tilstrekkelig med 0,005 til 1 volum-%, fortrinnsvis 0,02 til 0,5 volum-%, beregnet på motordrivstoffet. In engine tests, it has been shown that even small amounts of the individual components in the additive exert an optimal effect on a normal fuel. Usually 0.005 to 1% by volume, preferably 0.02 to 0.5% by volume, calculated on the motor fuel is sufficient.
Den angjeldende mengde av de i tilsetningsmidlet foreliggende enkeltkomponenter retter seg vidtgående etter den ønskede konsentrasjon av enkeltkomponentene i motordrivstoffet og etter mengden av tilsetningsmidlet som skal tilføres drivstof-fet. The relevant quantity of the individual components present in the additive largely depends on the desired concentration of the individual components in the motor fuel and on the amount of the additive to be added to the fuel oil.
Tilsetningsmidlet kan i tillegg til mineraloljeraffinater også inneholde syntetiske alifatiske hydrokarboner slik som "kogasin" og også syntetiske eller naturlige aromatiske hydrokarboner slik som alkylbenzoler. Tilsetningsmidlene kan videre inneholde andre stoffer slik som f.eks. korrosjonsinhi-bitorer, tenningsakselatorer, oktantallforbedrere, antioksydan-ter, høytryktilsetningsstoffer, forbrenningskatalysatorer og lignende, alt sammen stoffer som vanligvis tilsettes til drivstoffer. In addition to mineral oil raffinates, the additive may also contain synthetic aliphatic hydrocarbons such as "cogasine" and also synthetic or natural aromatic hydrocarbons such as alkylbenzenes. The additives may also contain other substances such as e.g. corrosion inhibitors, ignition accelerators, octane number improvers, antioxidants, high pressure additives, combustion catalysts and the like, all substances which are usually added to fuels.
Claims (2)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH359074 | 1974-03-14 | ||
CH708074 | 1974-05-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
NO750823L true NO750823L (en) | 1975-09-16 |
Family
ID=25693383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO750823A NO750823L (en) | 1974-03-14 | 1975-03-11 |
Country Status (12)
Country | Link |
---|---|
JP (1) | JPS50132007A (en) |
BR (1) | BR7501487A (en) |
DD (1) | DD116260A5 (en) |
DE (1) | DE2511249A1 (en) |
DK (1) | DK102675A (en) |
FI (1) | FI750728A (en) |
FR (1) | FR2273058A1 (en) |
IT (1) | IT1030334B (en) |
LU (1) | LU72045A1 (en) |
NL (1) | NL7503061A (en) |
NO (1) | NO750823L (en) |
SE (1) | SE7502830L (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4204481A (en) * | 1979-02-02 | 1980-05-27 | Ethyl Corporation | Anti-wear additives in diesel fuels |
ES2017030A6 (en) * | 1989-07-26 | 1990-12-16 | Lascaray Sa | Additive compound for fuels intended for internal combustion engines |
NZ506262A (en) * | 1998-01-12 | 2003-10-31 | Deborah Wenzel | Composition as an additive to create clear stable solutions and microemulsions with a combustible liquid fuel to improve combustion |
GB2516862A (en) | 2013-08-01 | 2015-02-11 | M I Drilling Fluids Uk Ltd | Quaternary ammonium compounds and gas hydrate inhibitor compositions |
-
1975
- 1975-03-11 NO NO750823A patent/NO750823L/no unknown
- 1975-03-13 JP JP50030623A patent/JPS50132007A/ja active Pending
- 1975-03-13 DK DK102675A patent/DK102675A/da not_active Application Discontinuation
- 1975-03-13 DE DE19752511249 patent/DE2511249A1/en active Pending
- 1975-03-13 IT IT67635/75A patent/IT1030334B/en active
- 1975-03-13 LU LU72045A patent/LU72045A1/xx unknown
- 1975-03-13 SE SE7502830A patent/SE7502830L/xx not_active Application Discontinuation
- 1975-03-13 BR BR1489/75A patent/BR7501487A/en unknown
- 1975-03-13 FR FR7507918A patent/FR2273058A1/en active Granted
- 1975-03-13 FI FI750728A patent/FI750728A/fi not_active Application Discontinuation
- 1975-03-14 NL NL7503061A patent/NL7503061A/en unknown
- 1975-03-14 DD DD184780A patent/DD116260A5/xx unknown
Also Published As
Publication number | Publication date |
---|---|
DE2511249A1 (en) | 1975-09-25 |
FR2273058A1 (en) | 1975-12-26 |
NL7503061A (en) | 1975-09-16 |
DK102675A (en) | 1975-09-15 |
LU72045A1 (en) | 1975-08-20 |
DD116260A5 (en) | 1975-11-12 |
JPS50132007A (en) | 1975-10-18 |
IT1030334B (en) | 1979-03-30 |
FR2273058B1 (en) | 1977-04-15 |
FI750728A (en) | 1975-09-15 |
BR7501487A (en) | 1975-12-16 |
SE7502830L (en) | 1975-09-15 |
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