CN109576009A - A kind of aqueous alcohol ethers diesel fuel and preparation method thereof - Google Patents
A kind of aqueous alcohol ethers diesel fuel and preparation method thereof Download PDFInfo
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- CN109576009A CN109576009A CN201811412730.7A CN201811412730A CN109576009A CN 109576009 A CN109576009 A CN 109576009A CN 201811412730 A CN201811412730 A CN 201811412730A CN 109576009 A CN109576009 A CN 109576009A
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- chain fatty
- diesel fuel
- alcohol ethers
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- fuel
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- 239000002283 diesel fuel Substances 0.000 title claims abstract description 62
- -1 alcohol ethers Chemical class 0.000 title claims abstract description 44
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 73
- 239000000446 fuel Substances 0.000 claims abstract description 39
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims abstract description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 13
- 238000003756 stirring Methods 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical group CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 12
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 239000012752 auxiliary agent Substances 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 150000002646 long chain fatty acid esters Chemical class 0.000 claims description 7
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- ARIWANIATODDMH-UHFFFAOYSA-N rac-1-monolauroylglycerol Chemical compound CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 claims description 6
- 150000005690 diesters Chemical class 0.000 claims description 5
- DCBSHORRWZKAKO-UHFFFAOYSA-N alpha-glycerol monomyristate Natural products CCCCCCCCCCCCCC(=O)OCC(O)CO DCBSHORRWZKAKO-UHFFFAOYSA-N 0.000 claims description 4
- 150000001721 carbon Chemical group 0.000 claims description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 4
- 229940068939 glyceryl monolaurate Drugs 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 238000005461 lubrication Methods 0.000 abstract description 4
- 238000000746 purification Methods 0.000 abstract description 4
- 239000003610 charcoal Substances 0.000 abstract description 3
- 230000000052 comparative effect Effects 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000003245 coal Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 5
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 4
- 235000009508 confectionery Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 239000006184 cosolvent Substances 0.000 description 2
- 238000006477 desulfuration reaction Methods 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 239000003502 gasoline Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 238000013400 design of experiment Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000004134 energy conservation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- DGPCSURYVBYWAT-UHFFFAOYSA-N propane-1,2,3-triol;tetradecanoic acid Chemical compound OCC(O)CO.CCCCCCCCCCCCCC(O)=O DGPCSURYVBYWAT-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000010148 water-pollination Effects 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
- C10L1/04—Liquid carbonaceous fuels essentially based on blends of hydrocarbons
-
- 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
- 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
-
- 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
- C10L1/1905—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polycarboxylic acids
-
- 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
- C10L1/1915—Esters ester radical containing compounds; ester ethers; carbonic acid esters complex esters (at least 3 ester bonds)
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- 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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
The present invention provides a kind of aqueous alcohol ethers diesel fuel and preparation method thereof, in the diesel oil containing fuel such as water, methanol, dimethyl ether, by the way that long-chain fatty alcohol is added, long chain fatty acids ester admixture carries out hydrotropy, lubrication, without carrying out purification process to the alcohol ethers class A fuel A such as methanol, it can be obtained stability height, lubricity is good, improves diesel oil service performance, reduce the novel environment friendly fuel of tail gas charcoal discharge amount, application value with higher.
Description
Technical field
The invention belongs to vehicle fuel technical fields, and in particular to a kind of aqueous alcohol ethers diesel fuel and its preparation
Method.
Background technique
Alcohol-ether fuel mainly includes methanol, dimethyl ether, is to be considered highly important substitute energy source for petroleum now, is also claimed
For coal-based alcohol ether fuel, the low-carbon oxygen-containing fuel mainly synthesized by coal by gasification, as widest automobile-used substitution vapour
The fuel of oil, diesel oil, not only increases comprehensive resource utilization rate, and be of great significance to reducing environmental pollution, meanwhile, by
The alcohol-ether fuel of coal conversion extremely meets the developing direction of coal conversion, coal gasification, has good economy.Currently, having had
Much the research that alcohol-ether fuel and gasoline, diesel oil are mixed with new fuel is reported.
Alcohol ether diesel oil for vehicles is formed in volume or weight than a certain proportion of alcohol ethers fuel formulations are added in diesel oil
A kind of environment friendly energy conservation fuel, however, during alcohol ether and diesel oil mix, it usually needs addition composite auxiliary solvent helps
Stable homogeneous system is formed, since alcohol ethers and diesel oil itself physicochemical property difference are larger, selects suitable cosolvent very
Key, studies have reported that adjusting the flash-point of alcohol ethers by water phase.But in the alcohol ethers diesel fuel for being added to water phase, according to
So there is a problem of stability difference, in order to improve its compatibility, also has been reported that addition includes acidic materials or the lipids such as oleic acid
The cosolvent of matter (such as ethyl acetate etc.) carries out hydrotropy, but unsatisfactory to the improvement of product stability.
And find in actual production, the substances such as methanol mixed with diesel oil can be emulsified when meeting water, it is general and
Speech, the full combustion of diesel oil can be promoted by forming Diesel Oil-methanol ternary emulsifying system, save petroleum resources, but its stability
It is not easy to control, so that oil plant is become muddy, whiten, or even generate floating material or flocculate, influences hybrid fuel appearance character, seriously
Ground even has an adverse effect to combustion chamber, pipeline, and some reasons are since impurity content is higher in the industrial production for methanol
Caused by, in general, the above problem can be improved by carrying out purifying upgrading processing to methanol, but production cost is improved simultaneously.Another party
Face, the alcohols materials such as methanol itself have stronger hydrophily, but its absorption moisture is more, poorer with the intersolubility of diesel oil, sternly
Important place can lead to oil layer, stability is poor.
China's Sulfur Content in Petroleum Products is higher at present, has aggravated the pollution level of automotive emission, has contained compared to gasoline
There is more impurity, it is easier to pollute environment, therefore deep desulfuration processing is carried out to diesel oil, it is miscellaneous that part is also removed while desulfurization
Matter.However, polycyclic aromatic hydrocarbon nitrogenous compound, the sulphur-containing substance etc. in diesel oil have certain influence to the lubricity of diesel oil, these
After devolatilization, diesel fuel lubricity is deteriorated, and causes motor car engine serious wear.
Summary of the invention
In order to solve the above technical problems, the present invention provides a kind of aqueous alcohol ethers diesel fuel, contain water, first described
In the diesel oil of the fuel such as alcohol, dimethyl ether, by the way that long-chain fatty alcohol is added, long chain fatty acids ester admixture carries out hydrotropy, lubrication, nothing
Purification process need to be carried out to the alcohol ethers class A fuel A such as methanol, can be obtained stability height, lubricity is good, diesel oil service performance is improved,
Reduce the novel environment friendly fuel of tail gas charcoal discharge amount, application value with higher.
On the one hand, the present invention provides a kind of aqueous alcohol ethers diesel fuel, and in parts by weight, the fuel includes:
Preferably, in parts by weight, the aqueous alcohol ethers diesel fuel includes:
Wherein, the auxiliary agent is the mixture of long-chain fatty alcohol and long-chain fatty acid ester, in aqueous alcohol ether of the invention
Hydrotropy, wear-resisting, synergism characteristic are played in class diesel fuel, contributes to form stable solution, increase the fuel to the packet of water
Capacitive makes the additive amount of water reach nearly 20%, while enhancing the lubricity of fuel, reduces the abrasion to engine.
Preferably, the long-chain fatty alcohol is the chain fatty alcohol with 6-18 carbon atom, such as Lauryl Alcohol, 14
Carbon alcohol, the pure and mild octadecanol of 16 carbon;The long-chain fatty acid ester is to be formed by the fatty acid with 6-18 carbon atom with alcohol
Monoesters or polyester, such as glycerol stearate monoesters, palmitinic acid fourth diester, Glyceryl Monolaurate, myristic acid glycerol list
Ester, Trivent OCG etc..Inventor has found that the mixability of the auxiliary agent is more complicated, to shape by orthonormal design of experiments
Higher at the effect of stablizing solution, that is, the ingredient mixed is more, and fuel is more stable, and as contained acids object in the auxiliary agent
Matter can destroy the stability of fuel, may be since acid and the Cucumber in diesel oil, methanol fuel, dimethyl ether fuel (can
Can be alkaline matter) it is reacted.
Preferably, the weight ratio of the long-chain fatty alcohol and long-chain fatty acid ester is 1:1-3.
Diesel oil used in the present invention is preferably national standard diesel oil, such as No. 5 derv fuels, No. 0 derv fuel ,-No. 10 vehicles
With diesel oil, in the case where the improvement of auxiliary agent helps, the addition of water, alcohol ether class A fuel A will not significantly improve the condensation point of diesel oil, especially solidifying
The higher diesel product of point.
Methanol used in the present invention is industrial methanol, can be manufactured by methods known in the art, such as can be by
The preparation such as natural gas, coal bed gas, oven gas, and denatured alcohol auxiliary agent can be wherein added, the industrial methanol needs not move through spy
Different purification process, but the content of methanol need to be in 75% or more, preferably 80-85%.Similarly, dimethyl ether used in the present invention
The industrial dimethyl ether that can be manufactured by methods known in the art, wherein the purity of dimethyl ether is 70% or more.
Without limitation, it can also be added and other commonly add in aqueous alcohol ethers diesel fuel of the invention in fuel
Add agent, such as ignition improver, antidetonation catalyst, rubber accelerator, antioxidant etc., condition is not influence the burning spy of fuel
Property.
On the other hand, the present invention also provides the preparation method of above-mentioned aqueous alcohol ethers diesel fuel, the method includes
Auxiliary agent is heated to 40-50 DEG C, is passed through in the stirring at normal temperature tank equipped with diesel oil, is added methanol, dimethyl ether, water, be sufficiently stirred
It is uniformly mixed, stands and obtain stable liquid, as aqueous alcohol ethers diesel fuel.
Technical solution of the present invention has the advantages that
In the diesel oil containing fuel such as water, methanol, dimethyl ether, by the way that long-chain fatty alcohol, long chain fatty acids is added
Ester admixture carries out hydrotropy, lubrication, without carrying out purification process to the alcohol ethers class A fuel A such as methanol, can be obtained stability height, profit
The good novel environment friendly fuel of slip improves water content, increases hybrid fuel in transport, cargo handling process to the containment of water.Together
When, added long-chain fatty alcohol, long chain fatty acids ester admixture auxiliary agent have the function of hydrotropy, lubrication, improve the resistance to of diesel oil
Mill property reduces the abrasion to engine, to attributes such as condensation point, the flash-points of fuel without damaging influence.And compared to common bavin
For oil, due to being mixed into the water and alcohol ether class A fuel A of nearly half weight, diesel oil service performance is improved, the discharge of tail gas charcoal is reduced
Amount, and character is stablized, application value with higher.
Specific embodiment
Invention is further explained combined with specific embodiments below, but it should be recognized that following embodiment is only
It is exemplary illustration, does not represent limitation of the present invention.
Embodiment 1
1.5kg Lauryl Alcohol, 16 carbon alcohol of 1.2kg, 1.2kg octadecanol, ten four carbon alcohols of 1.1kg, 2kg stearic acid is sweet
Oily monoesters, 2.5kg palmitinic acid fourth diester, 3.5kg Trivent OCG, 2kg myristic acid monoglyceride mix in mixing tank,
It is heated to 50 DEG C to be pumped into the stirring at normal temperature tank equipped with 0.5 ton of No. 5 diesel oil, 180kg industrial methanol, 130kg work is pumped under stirring
Industry dimethyl ether and 130kg water are thoroughly mixed uniformly, stand and obtain aqueous alcohol ethers diesel fuel.
Embodiment 2
By 5kg octadecanol, 4kg glycerol stearate monoesters, 4kg Glyceryl Monolaurate, 2kg myristic acid monoglyceride
It is mixed in mixing tank, is heated to 45 DEG C and is pumped into the stirring at normal temperature tank equipped with 0.6 ton of No. 0 diesel oil, 150kg work is pumped under stirring
Industry methanol, 120kg industry dimethyl ether and 150kg water are thoroughly mixed uniformly, stand and obtain aqueous alcohol ethers diesel fuel.
Embodiment 3
By 3kg Lauryl Alcohol, ten four carbon alcohols of 1kg, 16 carbon alcohol of 1kg, 5kg Trivent OCG, 8kg palmitinic acid fourth two
Ester, 2kg myristic acid monoglyceride mix in mixing tank, are heated to 48 DEG C and are pumped into the room temperature equipped with 0.45 ton of-No. 10 diesel oil
In agitator tank, it is pumped into 200kg industrial methanol, 120kg industry dimethyl ether and 120kg water under stirring, is thoroughly mixed uniformly, it is quiet
It sets and obtains aqueous alcohol ethers diesel fuel.
Embodiment 4
16 carbon alcohol of 2kg, 3kg octadecanol, 2kg glycerol stearate monoesters, 2kg palmitinic acid fourth diester, 1kg octanoic acid is sweet
Oily three esters mix in mixing tank, are heated to 50 DEG C and are pumped into the stirring at normal temperature tank equipped with 0.5 ton of No. 0 diesel oil, are pumped under stirring
160kg industrial methanol, 140kg industry dimethyl ether and 120kg water are thoroughly mixed uniformly, stand and obtain aqueous alcohol ethers bavin
Oil fuel.
Comparative example 1
50g oleic acid, 50g glycerol stearate monoesters are mixed in mixing tank, 50 DEG C is heated to and is pumped into equipped with No. 0 bavin of 5kg
In the stirring at normal temperature tank of oil, it is pumped into 1.80kg industrial methanol, 1.30kg industry dimethyl ether and 1.30kg water under stirring, is sufficiently stirred
It is uniformly mixed, stands and obtain aqueous alcohol ethers diesel fuel.
Comparative example 2
100g ethyl acetate is pumped into the stirring at normal temperature tank equipped with No. 0 diesel oil of 5kg, 1.80kg industry is pumped under stirring
Methanol, 1.30kg industry dimethyl ether and 1.30kg water are thoroughly mixed uniformly, stand and obtain aqueous alcohol ethers diesel fuel.
Comparative example 3
16 carbon alcohol of 20g, 30g octadecanol, 20g glycerol stearate monoesters, 20g palmitinic acid fourth diester, 10g octanoic acid is sweet
Oily three esters mix in mixing tank, are heated to 50 DEG C and are pumped into the stirring at normal temperature tank equipped with No. 0 diesel oil of 5kg, are pumped under stirring
1.80kg industrial methanol, 1.30kg industry dimethyl ether and 2.20kg water are thoroughly mixed uniformly, stand and obtain aqueous alcohol ethers
Diesel fuel.
Stability observing test
The embodiment 1-4 and comparative example 1-3 aqueous alcohol ethers diesel fuel prepared is respectively sampled into 10mL, is fitted into test tube and puts
It sets under the conditions of normal temperature and pressure opening:
It places about 3 days, the sample of comparative example 1 starts muddiness occur, and other samples keep clear and transparent, quality is uniform;
It places about 2 weeks, the sample observation of comparative example 1 to flocculate, the sample observation of comparative example 3 is other to lighter
Sample keeps clear and transparent, quality is uniform;
It places about 1 month, the sample flocculate of comparative example 1 increases, and accounts for total volume about 1/5th, the sample of comparative example 2
Observe lighter;The sample of comparative example 3 is divided into two layers, and other samples keep colors constant, clear and transparent, quality is uniform;
It places about 3 months, the sample appearance shape of embodiment 1-4 is almost unchanged.
Fuel performance test
The embodiment 1-4 and comparative example 1-3 aqueous alcohol ethers diesel fuel prepared is tested for the property, as a result such as following table
1 and table 2 shown in:
Table 1
Project | Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | Test method |
Condensation point/DEG C | 5 | -1 | -10 | 0 | GB/T510 |
Flash-point (silent)/DEG C | 62 | 60 | 63 | 61 | GB/T261 |
Lubricity | 440 | 448 | 452 | 455 | SH/T0765 |
Cetane number | 63 | 62 | 58 | 61 | GB/T386 |
Table 2
Project | Comparative example 1 | Comparative example 2 | Comparative example 3 | Test method |
Condensation point/DEG C | 0 | 0 | 2 | GB/T510 |
Flash-point (silent)/DEG C | 60 | 60 | 61 | GB/T261 |
Lubricity | 463 | 460 | 477 | SH/T0765 |
Cetane number | 53 | 49 | 42 | GB/T386 |
Above only describes better embodiments of the invention, but the present invention is not limited to above-described embodiments.This field skill
Art personnel should all fall into the present invention it is understood that can be realized any same or similar means of the technology of the present invention effect
Protection scope in.
Claims (8)
1. a kind of aqueous alcohol ethers diesel fuel, in parts by weight, the fuel includes:
Wherein, the auxiliary agent is the mixture of long-chain fatty alcohol and long-chain fatty acid ester.
2. aqueous alcohol ethers diesel fuel according to claim 1, wherein in parts by weight, the fuel includes:
3. aqueous alcohol ethers diesel fuel according to claim 1 or 2, wherein the long-chain fatty alcohol is with 6-18
The chain fatty alcohol of a carbon atom.
4. aqueous alcohol ethers diesel fuel according to claim 3, wherein the long-chain fatty alcohol is Lauryl Alcohol, ten
Four carbon alcohols, 16 carbon alcohol, octadecanol or their any mixture.
5. aqueous alcohol ethers diesel fuel according to claim 3, wherein the long-chain fatty acid ester is by with 6-18
The monoesters or polyester that the fatty acid and alcohol of a carbon atom are formed.
6. aqueous alcohol ethers diesel fuel according to claim 5, wherein the long-chain fatty acid ester is glycerol stearate
Monoesters, palmitinic acid fourth diester, Glyceryl Monolaurate, myristic acid monoglyceride, Trivent OCG or any of theirs mix
Close object.
7. aqueous alcohol ethers diesel fuel according to claim 3, wherein the long-chain fatty alcohol and long-chain fatty acid ester
Weight ratio be 1:1-3.
8. the preparation method of aqueous alcohol ethers diesel fuel of any of claims 1-7, the method includes helping
Agent is heated to 40-50 DEG C, is passed through in the stirring at normal temperature tank equipped with diesel oil, adds methanol, dimethyl ether, water, be thoroughly mixed
Uniformly, it stands and obtains stable liquid, as aqueous alcohol ethers diesel fuel.
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Citations (4)
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CN1147830A (en) * | 1994-04-04 | 1997-04-16 | 鲁道夫W·冈纳曼 | Aqueous fuel for internal combustion engine and preparation method thereof |
CN101538490A (en) * | 2009-04-30 | 2009-09-23 | 合肥工业大学 | Micro-emulsified biomass fuel and preparation method thereof |
CN107099345A (en) * | 2017-03-31 | 2017-08-29 | 兰州燚能生物科技有限责任公司 | Biological alcohol-based fuel oil hydrotropy solubilizer |
CN108546575A (en) * | 2018-05-15 | 2018-09-18 | 杨勇 | Biological alcohol-based fuel oil hydrotropy solubilizer |
-
2018
- 2018-11-26 CN CN201811412730.7A patent/CN109576009A/en not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1147830A (en) * | 1994-04-04 | 1997-04-16 | 鲁道夫W·冈纳曼 | Aqueous fuel for internal combustion engine and preparation method thereof |
CN101538490A (en) * | 2009-04-30 | 2009-09-23 | 合肥工业大学 | Micro-emulsified biomass fuel and preparation method thereof |
CN107099345A (en) * | 2017-03-31 | 2017-08-29 | 兰州燚能生物科技有限责任公司 | Biological alcohol-based fuel oil hydrotropy solubilizer |
CN108546575A (en) * | 2018-05-15 | 2018-09-18 | 杨勇 | Biological alcohol-based fuel oil hydrotropy solubilizer |
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