CN116515539A - Preparation method of high-clean fuel and high-clean fuel - Google Patents
Preparation method of high-clean fuel and high-clean fuel Download PDFInfo
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- CN116515539A CN116515539A CN202310643827.3A CN202310643827A CN116515539A CN 116515539 A CN116515539 A CN 116515539A CN 202310643827 A CN202310643827 A CN 202310643827A CN 116515539 A CN116515539 A CN 116515539A
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- isoamylene
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- 239000000446 fuel Substances 0.000 title claims abstract description 95
- 238000002360 preparation method Methods 0.000 title abstract description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 132
- 239000000203 mixture Substances 0.000 claims abstract description 120
- 238000002156 mixing Methods 0.000 claims abstract description 77
- 238000003756 stirring Methods 0.000 claims abstract description 45
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000003208 petroleum Substances 0.000 claims abstract description 43
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 claims abstract description 42
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 claims abstract description 41
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 claims abstract description 41
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 40
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 40
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 40
- 239000000654 additive Substances 0.000 claims abstract description 31
- 230000000996 additive effect Effects 0.000 claims abstract description 31
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims abstract description 23
- 239000003245 coal Substances 0.000 claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 238000005507 spraying Methods 0.000 claims abstract description 4
- 239000008096 xylene Substances 0.000 claims description 37
- 239000002994 raw material Substances 0.000 claims description 28
- 238000001914 filtration Methods 0.000 claims description 18
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 13
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 13
- -1 polyoxyethylene Polymers 0.000 claims description 13
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 claims description 12
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 12
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 12
- 238000009775 high-speed stirring Methods 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 abstract description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 17
- 230000015572 biosynthetic process Effects 0.000 abstract description 17
- 229910052799 carbon Inorganic materials 0.000 abstract description 17
- 230000008021 deposition Effects 0.000 abstract description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 60
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 21
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 20
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 20
- 229910052760 oxygen Inorganic materials 0.000 description 20
- 239000001301 oxygen Substances 0.000 description 20
- 229910052717 sulfur Inorganic materials 0.000 description 20
- 239000011593 sulfur Substances 0.000 description 20
- 239000003502 gasoline Substances 0.000 description 15
- 238000011109 contamination Methods 0.000 description 13
- 239000003673 groundwater Substances 0.000 description 13
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- NPZDCTUDQYGYQD-UHFFFAOYSA-N 1-tritylimidazole Chemical compound C1=NC=CN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 NPZDCTUDQYGYQD-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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- GMEONFUTDYJSNV-UHFFFAOYSA-N Ethyl levulinate Chemical compound CCOC(=O)CCC(C)=O GMEONFUTDYJSNV-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-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
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-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
- 239000003381 stabilizer Substances 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/04—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
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/1955—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by an alcohol, ether, aldehyde, ketonic, ketal, acetal radical
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
The invention discloses a preparation method of a high-cleanness fuel, which comprises the following steps: under the heating condition, injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at high speed for mixing, and simultaneously spraying high-pressure air into the container to obtain a first mixture; mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30-60 ℃ to obtain a second mixture; mixing petroleum mixed dimethylbenzene with the second mixture, adding an additive, and stirring at a high speed under ultrasonic conditions to obtain a third mixture; the third mixture is centrifugally separated and filtered, so that the production cost of the high-clean fuel obtained by the method is far lower than that of the existing fuel, the combustion is more sufficient, the carbon deposition formation is reduced, the pollution of combustion residues to underground water quality is improved, and the high-clean fuel is more environment-friendly than the existing fuel.
Description
Technical Field
The invention relates to the technical field of chemical products, in particular to a preparation method of a high-clean fuel and the high-clean fuel.
Background
With the development of world economy, the demand for fuel is increasing, and the traditional resources such as diesel, gasoline, natural gas and the like are becoming deficient. According to the statistics of world petroleum peak, world petroleum can be exploited for 32 years for commercial use, so the development of novel high-cleanness alternative energy sources becomes a main direction of the development of the future energy source field.
Meanwhile, the exhaust emission of motor vehicles has become a main pollution source in large cities around the world. The environmental pollution of gasoline vehicles is more serious than gasoline vehicles, and more vehicles and various internal combustion engines use gasoline.
The existing high-cleanness gasoline is prepared by chemical raw materials, base component oil (89 # gasoline), methyl Tertiary Butyl Ether (MTBE), alkylate oil and aromatic hydrocarbons in proportion. The existing gasoline has high production cost, the antiknock MTBE is difficult to degrade, and the water source is polluted.
Disclosure of Invention
The invention aims to provide a preparation method of a high-cleanness fuel, which solves the problems that an antiknock MTBE is difficult to degrade and pollutes the environment in the prior art.
To solve the above problems, a first aspect of the present invention provides a method for preparing a highly clean fuel, comprising:
under the heating condition, injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at high speed for mixing, and simultaneously spraying high-pressure air into the container to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30-60 ℃ to obtain a second mixture;
mixing petroleum mixed dimethylbenzene with the second mixture, adding an additive, and stirring at a high speed under ultrasonic conditions to obtain a third mixture;
centrifugally separating and filtering the third mixture to obtain a high-clean fuel;
the mass ratio of the raw materials is as follows: stable light hydrocarbon (30-42%), isooctane (10-20%), aromatic hydrocarbon (15-20%), petroleum mixed xylene (20-28%), isoamylene (8-12%), additive (0.01-0.02%) and methanol (4-15%).
Optionally, the additive is dodecyl polyoxyethylene alcohol or dodecyl benzene polyoxyethylene ether.
Optionally, the heating condition is 25 ℃ to 50 ℃.
Optionally, the time for spraying the high-pressure air into the container is 5-10min, and the air pressure of the high-pressure air is 35-100kpa.
Optionally, the rotating speed of the closed container is 1000r/min-3000r/min;
the stirring speed under the ultrasonic condition is 2500r/min-5000r/min.
Optionally, the first mixture is mixed with isooctane and isoamylene and then placed in a closed environment and stirred at 52 ℃.
Optionally, the mass ratio of the raw materials is as follows: 38% of stable light hydrocarbon, 12% of isooctane, 15% of coal-to-aromatic hydrocarbon, 21% of petroleum mixed xylene, 9% of isoamylene, 0.02% of additive and 4.98% of methanol.
Alternatively, the stirring time for high-speed stirring under ultrasonic conditions is 10 to 20 minutes.
In another aspect, the present invention provides a highly clean fuel prepared by the method of preparing a highly clean fuel as described above.
The technical scheme of the invention has the following beneficial technical effects:
the production cost of the high-clean fuel obtained by the preparation method of the high-clean fuel is far lower than the existing production cost, the combustion is more sufficient, the formation of carbon deposition is reduced, the pollution of combustion residues to underground water quality is improved, and compared with the existing fuel, the high-clean fuel is more environment-friendly, and the contents of benzene, oxygen and sulfur are lower than the national standard by 50%. Meanwhile, the high clean fuel obtained based on the method has good layering resistant effect, and the water content increase of the bottom layer solution is far lower than that of the prior commercial gasoline after the wide-mouth bottle is stored for 30 days.
Drawings
FIG. 1 is a flow chart of a method for preparing a highly clean fuel according to the present invention.
Detailed Description
The objects, technical solutions and advantages of the present invention will become more apparent by the following detailed description of the present invention with reference to the accompanying drawings. It should be understood that the description is only illustrative and is not intended to limit the scope of the invention. In addition, in the following description, descriptions of well-known structures and techniques are omitted so as not to unnecessarily obscure the present invention.
It will be apparent that the described embodiments are some, but not all, embodiments of the invention. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
In the description of the present invention, it should be noted that the terms "first," "second," and "third" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
In addition, the technical features of the different embodiments of the present invention described below may be combined with each other as long as they do not collide with each other.
The existing high-cleanness gasoline is prepared by chemical raw materials, base component oil (89 # gasoline), MTBE, alkylate oil and aromatic hydrocarbons in proportion. The existing gasoline has high production cost, the antiknock MTBE is difficult to degrade, and the water source is polluted.
The invention provides a preparation method of a high-cleanness fuel, which comprises the following steps:
under the heating condition, the stable light hydrocarbon, the coal aromatic hydrocarbon and the methanol are injected into a closed container rotating at a high speed for mixing, and high-pressure air is sprayed into the container at the same time, so that a first mixture is obtained. Wherein, the heating condition can be 25 ℃ to 50 ℃, and is preferably 50 ℃; the rotary closed container can be a rotary airflow mixer, the inner cylinder wall of the rotary airflow mixer is provided with an impeller, liquid and gas are respectively conveyed into the rotary airflow mixer through two pipelines, and the impeller mixes the gas and the liquid through rotation; in this embodiment, the rotation speed of the closed container is 1000r/min-3000r/min, preferably 3000r/min; the mixing time is 5-10min, and the high-temperature and high-pressure environment for oxidation reaction is formed by rotating at high speed in a closed container and introducing air, so that the full mixing of various raw materials is realized.
Mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30-60 ℃ to obtain a second mixture. The closed environment here can be achieved by placing the mixture in a vacuum closed container, preferably at a temperature of 52 ℃. Mixing in a vacuum sealed container prevents the raw materials from volatilizing to cause proportion imbalance, and prevents other impurities from being mixed.
Mixing petroleum mixed xylene with the second mixture, adding an additive, and stirring at high speed under ultrasonic conditions for 10-20min to obtain a third mixture; in the embodiment, the additive adopts the dodecyl polyoxyethylene alcohol or the dodecyl benzene polyoxyethylene ether, and the dodecyl polyoxyethylene alcohol or the dodecyl benzene polyoxyethylene ether is used as the additive, so that a better anti-layering effect can be achieved, and particularly, the water precipitation in the mixture can be prevented. Centrifugally separating and filtering the third mixture to obtain a high-clean fuel;
the mass ratio of the raw materials is as follows: the mass ratio of the raw materials is as follows: 38% of stable light hydrocarbon, 12% of isooctane, 15% of coal-to-aromatic hydrocarbon, 21% of petroleum mixed xylene, 9% of isoamylene, 0.02% of additive and 4.98% of methanol.
In another aspect, the present invention provides a highly clean fuel prepared by the method of preparing a highly clean fuel as described above.
Specific examples and comparative examples are provided below to illustrate in detail the methods provided by the present invention.
Example 1
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 25 ℃ and injecting high-pressure air of 35kpa into the container, wherein the mixing time is 10min, and the rotating speed of the closed container is 2000r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30 ℃ for 10min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 10 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 22% of petroleum mixed xylene, 8% of isoamylene, 0.01% of additive and 14.99% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 98, the combustion value was 12034kcal/kg, the benzene content was 0.4g/kwh, the oxygen content was 1.35g/kwh, the sulfur content was 5g/kwh, and the increase in water content of the underlying solution was 35 μg g after 30 days of jar rest ―1 。
Example 2
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 50 ℃ and injecting 70kpa of high-pressure air into the container, wherein the mixing time is 10min, and the rotating speed of the closed container is 3000r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 35 ℃ for 15min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 20 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 38% of stable light hydrocarbon, 12% of isooctane, 15% of coal-to-aromatic hydrocarbon, 21% of petroleum mixed xylene, 9% of isoamylene, 0.02% of additive and 4.98% of methanol.
The high clean fuel obtained by the embodiment has far lower production cost than the prior production cost, more complete combustion, reduced carbon deposition formation, improved pollution of combustion residues to underground water quality, and more environmental protection compared with the prior fuel, wherein the octane number is 97, the combustion value is 12220kcal/kg, and the benzene content0.38g/kwh, 1.0g/kwh oxygen content, 4.8g/kwh sulfur content, and 32 μg×g water content increase after 30 days of jar standing ―1 。
Example 3
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 35 ℃ and injecting high-pressure air of 60kpa into the container, wherein the mixing time is 8min, and the rotating speed of the closed container is 2300r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 45 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 12 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 42% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 20.99% of petroleum mixed xylene, 8% of isoamylene, 0.01% of additive and 4% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 95, the combustion value was 12340kcal/kg, the benzene content was 0.35g/kwh, the oxygen content was 1.23g/kwh, the sulfur content was 3.5g/kwh, and the water content of the primer solution increased by 38 μg g after 30 days of standing in a jar ―1 。
Example 4
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 25 ℃ and injecting high-pressure air of 35kpa into the container, wherein the mixing time is 6min, and the rotating speed of the closed container is 2500r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 35 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 13 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 37% of stable light hydrocarbon, 11% of isooctane, 16% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 10% of isoamylene, 0.01% of additive and 5.99% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 97, the combustion value was 12230kcal/kg, the benzene content was 0.36g/kwh, the oxygen content was 1.31g/kwh, the sulfur content was 4.4g/kwh, and the water content of the primer solution was 37 μg after 30 days of standing in a jar ―1 。
Example 5
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 50 ℃ and injecting 80kpa of high-pressure air into the container, wherein the mixing time is 8min, and the rotating speed of the closed container is 2800r/min to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 45 ℃ for 14min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 18 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 12% of isooctane, 15% of coal-to-aromatic hydrocarbon, 26% of petroleum mixed xylene, 10% of isoamylene, 0.02% of additive and 6.98% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 98, the combustion value was 11903kcal/kg, the benzene content was 0.37g/kwh, the oxygen content was 1.32g/kwh, the sulfur content was 3.5g/kwh, and the water content of the primer solution increased by 36 μg g after 30 days of standing in a jar ―1 。
Example 6
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 45 ℃ and injecting high-pressure air of 75kpa into the container at the same time, wherein the mixing time is 5min, and the rotating speed of the closed container is 2500r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 45 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 13 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 18% of isooctane, 18% of coal-to-aromatic hydrocarbon, 23% of petroleum mixed xylene, 8% of isoamylene, 0.02% of additive and 10.98% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 96, the combustion value was 12093kcal/kg, the benzene content was 0.39g/kwh, the oxygen content was 1.28g/kwh, the sulfur content was 3.7g/kwh, and the water content of the primer solution increased by 42 μg g after 30 days of standing in a jar ―1 。
Example 7
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 35 ℃ and injecting 80kpa of high-pressure air into the container, wherein the mixing time is 7min, and the rotating speed of the closed container is 2300r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 60 ℃ for 12min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 15 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 38% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 8.5% of isoamylene, 0.01% of additive and 8.49% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 99, the combustion value was 12322kcal/kg, the benzene content was 0.32g/kwh, the oxygen content was 1.21g/kwh, the sulfur content was 4.7g/kwh, and the water content of the primer solution increased by 45 μg g after 30 days of standing in a jar ―1 。
Example 8
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 25 ℃ and injecting high-pressure air of 50kpa into the container, wherein the mixing time is 6min, and the rotating speed of the closed container is 2000r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 55 ℃ for 12min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecyl polyoxyethylene alcohol, and stirring at high speed under ultrasonic conditions for 16 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 15% of isooctane, 16% of coal-to-aromatic hydrocarbon, 22% of petroleum mixed xylene, 9% of isoamylene, 0.01% of additive and 7.99% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 108, the combustion value was 12320kcal/kg, the benzene content was 0.33g/kwh, the oxygen content was 1.18g/kwh, the sulfur content was 4.3g/kwh, and the water content of the primer solution increased by 45 μg g after 30 days of jar rest ―1 。
Example 9
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 25 ℃ and injecting high-pressure air of 85kpa into the container, wherein the mixing time is 8min, and the rotating speed of the closed container is 1600r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 37 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 16 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 35% of stable light hydrocarbon, 10% of isooctane, 18% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 9% of isoamylene, 0.015% of additive and 7.985% of methanol.
The high clean fuel obtained by the embodiment has far lower production cost than the prior production cost, more sufficient combustion, reduced carbon deposition formation, improved pollution of combustion residues to underground water quality, and more environmental protection compared with the prior fuel, wherein the octane number is 96, the combustion value is 13003kcal/kg, the benzene content is 0.38g/kwh, the oxygen content is 1.29g/kwh, the sulfur content is 4.8g/kwh, after the jar is left to stand for 30 days, the water content of the bottom layer solution is increased by 42 mug ―1 。
Example 10
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 40 ℃ and injecting high-pressure air of 65kpa into the container at the same time, wherein the mixing time is 8min, and the rotating speed of the closed container is 1300r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and then placing in a closed environment to stir at 38 ℃ for 15min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 15 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30.98% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 9% of isoamylene, 0.02% of additive and 15% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 97, the combustion value was 12890kcal/kg, the benzene content was 0.39g/kwh, the oxygen content was 1.33g/kwh, the sulfur content was 4.6g/kwh, and the water content of the primer solution increased by 39 μg g after 30 days of standing in a jar ―1 。
Example 11
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 27 ℃ and injecting high-pressure air of 95kpa into the container, wherein the mixing time is 7min, and the rotating speed of the closed container is 1000r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 33 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 14 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 28% of petroleum mixed xylene, 10% of isoamylene, 0.02% of additive and 6.98% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 96, the combustion value was 12870kcal/kg, the benzene content was 0.35g/kwh, the oxygen content was 1.26g/kwh, the sulfur content was 4.3g/kwh, and the water content of the primer solution was 37 μg after 30 days of standing in a jar ―1 。
Example 12
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 43 ℃ and injecting high-pressure air of 65kpa into the container at the same time, wherein the mixing time is 6min, and the rotating speed of the closed container is 2000r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30 ℃ for 13min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 17 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 10% of isooctane, 20% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 10% of isoamylene, 0.02% of additive and 9.98% of methanol.
The high clean fuel obtained by this example was much lower in cost than the existing fuel, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than the existing fuel, wherein the octane number was 93, the combustion value was 12730kcal/kg, the benzene content was 0.4g/kwh, the oxygen content was 1.32g/kwh, the sulfur content was 4.4g/kwh, and the water content of the primer solution was 38 μg after 30 days of standing in a jar ―1 。
Example 13
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 29 ℃ and injecting high-pressure air of 98kpa into the container, wherein the mixing time is 9min, and the rotating speed of the closed container is 2300r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 55 ℃ for 14min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 18 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 30% of stable light hydrocarbon, 20% of isooctane, 15% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 9.98% of isoamylene, 0.02% of additive and 5% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 99, the combustion value was 12543kcal/kg, the benzene content was 0.32g/kwh, the oxygen content was 1.33g/kwh, the sulfur content was 3.9g/kwh, and the water content of the primer solution was 36 μg/g after 30 days of standing in a jar ―1 。
Example 14
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 25 ℃ and injecting 80kpa of high-pressure air into the container, wherein the mixing time is 10min, and the rotating speed of the closed container is 2500r/min, so as to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30 ℃ for 14min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 16 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 40% of stable light hydrocarbon, 10% of isooctane, 15% of coal-to-aromatic hydrocarbon, 20% of petroleum mixed xylene, 8% of isoamylene, 0.02% of additive and 6.98% of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 97, the combustion value was 12658kcal/kg, the benzene content was 0.34g/kwh, the oxygen content was 1.28g/kwh, the sulfur content was 4.6g/kwh, and the water content of the primer solution increased by 33 μg g after 30 days of jar rest ―1 。
Example 15
Injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at a high speed for mixing at 45 ℃ and injecting high-pressure air of 70kpa into the container, wherein the mixing time is 6min, and the rotating speed of the closed container is 2800r/min to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring at 45 ℃ for 12min to obtain a second mixture;
mixing petroleum mixed xylene with the second mixture, adding dodecylbenzene polyoxyethylene ether, and stirring at high speed under ultrasonic conditions for 10 minutes to obtain a third mixture;
and centrifuging and filtering the third mixture to obtain the high-cleanliness fuel.
The mass ratio of the raw materials is as follows: 32.99 percent of stable light hydrocarbon, 12 percent of isooctane, 15 percent of coal-to-aromatic hydrocarbon, 26 percent of petroleum mixed xylene, 9 percent of isoamylene, 0.01 percent of additive and 5 percent of methanol.
The high clean fuel obtained by this example was far lower in cost than existing, burned more fully, reduced in carbon formation, improved in contamination of the groundwater quality by combustion residues, and more environmentally friendly than existing fuels, wherein the octane number was 96, the combustion value was 12655kcal/kg, the benzene content was 0.32g/kwh, the oxygen content was 1.25g/kwh, the sulfur content was 4.7g/kwh, and the water content of the primer solution increased by 40 μg g after 30 days of standing in a jar ―1 。
Comparative example 1
The fuel for the vehicle is prepared from the following raw materials in parts by weight: 15 parts of amyl alcohol, 10 parts of isobutanol, 35 parts of n-octane, 10 parts of ethyl levulinate, 8 parts of 1-trityl imidazole, 1 part of a detergent and 0.5 part of a combustion improver; the detergent is a mixture of 30 parts by weight of 2-methylimidazole and 3 parts by weight of ethylene glycol butyl ether; the combustion improver is a mixture of 28 parts by weight of dimethyl carbonate and 1 part by weight of ethyl tertiary butyl ether.
The preparation method of the vehicle fuel comprises the following steps: mixing amyl alcohol, isobutanol, n-octane, ethyl levulinate and 1-trityl imidazole uniformly, stirring for 55min, adding a detergent and a combustion improver, continuously stirring for 30min, vacuumizing, and standing for 15 h.
The obtained fuel had an octane number of 98, a combustion value of 10659kcal/kg, a benzene content of 0.9g/kwh, an oxygen content of 2.66g/kwh, a sulfur content of 11g/kwh, and after 30 days of standing in a jar, the water content of the base solution increased by 423 μg ―1 。
Comparative example 2
The methanol gasoline comprises the following components in percentage by mass: 73-75% of methanol, 0.004-0.006% of sodium hydroxide, 0.3-0.5% of corrosion inhibitor, 0.2-0.4% of antioxidant, 0.5-0.7% of lubricant, 3-4% of methyl tertiary butyl ether, 3-5% of petroleum ether, 0.4-0.6% of cyclohexylamine, 7-9% of naphtha, 4-6% of low-temperature ignition additive and 2-2.5% of stabilizer, wherein the stabilizer comprises butanone and glycerol, the mass ratio of the butanone to the glycerol is 2:3, the corrosion inhibitor comprises benzotriazole and oleic acid imidazoline, and the mass ratio of the benzotriazole to the oleic acid imidazoline is 2:3.
The preparation method of the methanol gasoline comprises the following steps: all the raw materials are mixed and stirred uniformly.
The obtained fuel had an octane number of 96, a combustion value of 11398kcal/kg, a benzene content of 0.82g/kwh, an oxygen content of 2.73g/kwh, a sulfur content of 12g/kwh, and an increase in water content of 382 μg after 30 days of standing in a jar ―1 . The high clean fuels prepared in examples 1 to 15 and the fuels prepared in comparative examples 1 and 2 were subjected to the related experiments, respectively, and the results are shown in table 1:
table 1 high clean fuel comparative experiment table
The experimental data show that the high clean fuel obtained by the preparation method of the high clean fuel adopted in the embodiment of the invention has obviously reduced benzene content, oxygen content, sulfur content and the like, and is reduced by more than 50 percent compared with the prior gasoline fuel and national standard.
The high-cleanness fuel oil provided by the embodiment of the invention replaces the traditional naphtha with the stable light hydrocarbon, the heat value is higher than that of the traditional naphtha, and the evaporation performance is higher than that of the common naphtha; isoamylene provides olefin content while increasing the combustion heating value; the additive can better combine the problem of fusion of methanol and chemical raw materials; the petroleum mixed xylene has high combustion speed and is also an effective organic solvent; the coal-to-aromatics contains 10% -30% of olefin, the aromatics content reaches 50% -70%, and the aromatics content is normally provided, meanwhile, the olefins are effectively supplemented, and the combustion heat value is improved. Based on the addition of the additive dodecyl polyoxyethylene alcohol or dodecyl benzene polyoxyethylene ether, the delamination resistance effect is better.
The invention solves the problem that the traditional methanol gasoline is difficult to dissolve, has weak low-temperature resistance and low combustion heat value. The petrochemical industry and the coal chemical industry are combined, so that the tradition is broken through; improving the pollution of combustion residues to underground water quality; the invention better meets the environmental protection requirement (the contents of benzene, oxygen and sulfur are lower than the national standard requirement by 50%), and simultaneously can reduce the production cost.
It is to be understood that the above-described embodiments of the present invention are merely illustrative of or explanation of the principles of the present invention and are in no way limiting of the invention. Accordingly, any modification, equivalent replacement, improvement, etc. made without departing from the spirit and scope of the present invention should be included in the scope of the present invention. Furthermore, the appended claims are intended to cover all such changes and modifications that fall within the scope and boundary of the appended claims, or equivalents of such scope and boundary.
Although embodiments of the present invention have been described in detail, it should be understood that various changes, substitutions, and alterations can be made hereto without departing from the spirit and scope of the invention.
It is apparent that the above examples are given by way of illustration only and are not limiting of the embodiments. Other variations or modifications of the above teachings will be apparent to those of ordinary skill in the art. It is not necessary here nor is it exhaustive of all embodiments. While still being apparent from variations or modifications that may be made by those skilled in the art are within the scope of the invention.
The steps in the method of the embodiment of the invention can be sequentially adjusted, combined and deleted according to actual needs.
Claims (9)
1. A method for preparing a highly clean fuel, comprising:
under the heating condition, injecting stable light hydrocarbon, coal aromatic hydrocarbon and methanol into a closed container rotating at high speed for mixing, and simultaneously spraying high-pressure air into the container to obtain a first mixture;
mixing the first mixture with isooctane and isoamylene, and stirring in a closed environment at 30-60 ℃ to obtain a second mixture;
mixing petroleum mixed dimethylbenzene with the second mixture, adding an additive, and stirring at a high speed under ultrasonic conditions to obtain a third mixture;
centrifugally separating and filtering the third mixture to obtain a high-clean fuel;
the mass ratio of the raw materials is as follows: stable light hydrocarbon (30-42%), isooctane (10-20%), aromatic hydrocarbon (15-20%), petroleum mixed xylene (20-28%), isoamylene (8-12%), additive (0.01-0.02%) and methanol (4-15%).
2. The method for producing a highly clean fuel according to claim 1, characterized in that,
the additive is dodecyl polyoxyethylene alcohol or dodecyl benzene polyoxyethylene ether.
3. The method for producing a highly clean fuel according to claim 1, characterized in that,
the heating condition is 25-50 ℃.
4. The method for producing a highly clean fuel according to claim 3, wherein,
the mixing time in the high-speed rotating closed container is 5-10min, and the air pressure of the high-pressure air is 35-100kpa.
5. The method for producing a highly clean fuel according to claim 4, wherein,
the rotating speed of the closed container is 1000r/min-3000r/min;
the stirring speed under the ultrasonic condition is 2500r/min-5000r/min.
6. The method for producing a highly clean fuel according to claim 1, characterized in that,
the first mixture was mixed with isooctane and isoamylene and then placed in a closed environment with stirring at 52 ℃.
7. The method for producing a highly clean fuel according to claim 1, characterized in that,
the mass ratio of the raw materials is as follows: 38% of stable light hydrocarbon, 12% of isooctane, 15% of coal-to-aromatic hydrocarbon, 21% of petroleum mixed xylene, 9% of isoamylene, 0.02% of additive and 4.98% of methanol.
8. The method for producing a highly clean fuel according to claim 1, characterized in that,
the stirring time for high-speed stirring under the ultrasonic condition is 10-20 minutes.
9. A highly clean fuel, characterized in that the highly clean fuel is produced by the production method of the highly clean fuel according to any one of claims 1 to 8.
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