CN103131481B - A kind of biosynthesizing fuel - Google Patents
A kind of biosynthesizing fuel Download PDFInfo
- Publication number
- CN103131481B CN103131481B CN201110271789.0A CN201110271789A CN103131481B CN 103131481 B CN103131481 B CN 103131481B CN 201110271789 A CN201110271789 A CN 201110271789A CN 103131481 B CN103131481 B CN 103131481B
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- CN
- China
- Prior art keywords
- compound
- biosynthesizing
- making method
- normal temperature
- gas
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- 239000000446 fuel Substances 0.000 title claims abstract description 15
- 230000003570 biosynthesizing effect Effects 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 claims abstract description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000007788 liquid Substances 0.000 claims abstract description 12
- 239000002994 raw material Substances 0.000 claims abstract description 12
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000010438 heat treatment Methods 0.000 claims abstract description 9
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 claims abstract description 6
- 230000003197 catalytic effect Effects 0.000 claims abstract description 6
- 239000007789 gas Substances 0.000 claims abstract description 6
- -1 hydrogen Chemical class 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- JXAZAUKOWVKTLO-UHFFFAOYSA-L sodium pyrosulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OS([O-])(=O)=O JXAZAUKOWVKTLO-UHFFFAOYSA-L 0.000 claims abstract description 6
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 claims abstract description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000009472 formulation Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 150000001896 cresols Chemical class 0.000 abstract description 4
- 239000003995 emulsifying agent Substances 0.000 abstract description 4
- 239000002551 biofuel Substances 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- 239000003344 environmental pollutant Substances 0.000 abstract 1
- 231100000719 pollutant Toxicity 0.000 abstract 1
- 238000005516 engineering process Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- 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
- Y02E50/10—Biofuels, e.g. bio-diesel
Landscapes
- Liquid Carbonaceous Fuels (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The invention provides a kind of biosynthesizing fuel, methyl alcohol 42.97, ethanol 42.97, Viscotrol C 11.73, sodium pyrosulfate 1.46, ionic emulsifying agent 0.29, solubility promoter 0.29, cresols 0.29, described method point following steps are carried out: 1) above-mentioned raw materials is put into stirred pot together by weight feeding and be uniformly mixed; 2) compound stirred is put into reactor and be heated to 350 DEG C; 3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000Kg
3hydrogen, then be down to normal temperature by tubulation device; 4) compound being down to normal temperature sends into finished pot, by 5% of total amount add ferrocene and 10% octane value for biological synthol.Methyl alcohol and ethanol are synthesized biofuel by scientific approach by the present invention, have that calorific value is high, disposal of pollutants is low, cost is reasonable and raw material such as easily to obtain at the many advantages, are a kind of ideal synthesis energy of recyclability.
Description
Technical field
The present invention relates to a kind of synthol, specifically a kind of biosynthesizing fuel.
Background technology
Along with improving constantly of economy and standard of living; energy consumption constantly expands; non-renewable petroleum resources are day by day exhausted; its energy dilemma on the horizon; will affect and restrict the development of world economy; in order to meet the growing material life of people and Economic development needs; develop and develop new renewable energy source and become the task of top priority; input in science and technology is all being strengthened for reply energy dilemma and development research, particularly calorific value are high, discharge low renewable new forms of energy has become the urgent major issue that the mankind face in countries in the world.
Summary of the invention
The object of the invention is to solve the day by day exhausted present situation of current energy source, a kind of biosynthesizing fuel be provided, have calorific value high, discharge low, the rational distinguishing feature of cost, be a kind of scientific and reasonable renewable synthol.
The present invention includes the methyl alcohol, ethanol, Viscotrol C and the sodium pyrosulfate that use in synthol, the technical scheme adopted is:
Its formulation weight per-cent is as follows:
Another object of the present invention is to the making method providing a kind of above-mentioned biosynthesizing fuel, a main point following a few step is carried out:
1) above-mentioned raw materials is put into stirred pot together by weight feeding to be uniformly mixed;
2) compound stirred is put into reactor and be heated to 350 DEG C;
3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000Kg
3hydrogen, then be down to normal temperature by tubulation device;
4) compound being down to normal temperature sends into finished pot, by 5% of total amount add ferrocene and 10% octane value for biological synthol.
In above-mentioned making method:
Making method 1) in the time of stirring be 5 ~ 10 minutes.
Making method 2) in be heated to 350 DEG C, its air pressure should reach 4 pressure.
Technique scheme that the present invention passes through, because the main component in raw material have employed reproducible methyl alcohol and ethanol, and allocate a small amount of industrial chemicals into, simply synthesis is made again by science, produce biofuel after testing, its fuel value can reach 1.1 ten thousand kilocalories, the quantity discharged of hydrocarbon polymer and an oxidation is extremely low, calorific value is suitable with existing gasoline, can be applied directly in existing motor car engine and use as power fuel, raw material required for the present invention easily obtains, and making processes is simple, has fabulous popularizing application prospect.
Accompanying drawing explanation
Below in conjunction with drawings and Examples, the invention will be further described.
Accompanying drawing is present invention process schematic flow sheet.
Embodiment
Embodiment 1: calculate to make 500Kg biosynthesizing fuel, desired raw material in percentage terms weight is as follows: methyl alcohol 42.97% 214.85Kg, ethanol 42.97% 214.85Kg, Viscotrol C 11.73% 58.65Kg, sodium pyrosulfate 1.46% 7.3Kg, ionic emulsifying agent 0.29% 1.45Kg, solubility promoter 0.29% 1.45Kg, cresols 0.29% 1.45Kg
Making method is as follows:
1) above-mentioned raw materials is put into stirred pot together by weight feeding to be uniformly mixed;
2) compound stirred is put into reactor and be heated to 350 DEG C;
3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000Kg
3hydrogen, then be down to normal temperature by tubulation device;
4) compound being down to normal temperature sends into finished pot, by 5% of total amount add ferrocene and 10% octane value for biological synthol.
In above-mentioned making processes, method 1) in churning time be 5 minutes, method formula) in heating after press and exhaustedly reach 4 pressure.
Embodiment 2: calculate to make 1000Kg biosynthesizing fuel, desired raw material in percentage terms weight is as follows: methyl alcohol 42.97% 429.7Kg, ethanol 42.97% 429.7Kg, Viscotrol C 11.73% 117.3Kg, sodium pyrosulfate 1.46% 14.6Kg, ionic emulsifying agent 0.29% 2.9Kg, solubility promoter 0.29% 2.9Kg, cresols 0.29% 2.9Kg
Making method is as follows:
1) above-mentioned raw materials is put into stirred pot together by weight feeding to be uniformly mixed;
2) compound stirred is put into reactor and be heated to 350 DEG C;
3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000Kg
3hydrogen, then by tubulation device be down to normal temperature for biological synthol.
In above-mentioned making processes, method 1) in churning time be 8 minutes, method formula) in heating after press and exhaustedly reach 4 pressure.
Embodiment 3: calculate to make 2000Kg biosynthesizing fuel, desired raw material in percentage terms weight is as follows: methyl alcohol 42.97% 859.4Kg, ethanol 42.97% 859.4Kg, Viscotrol C 11.73% 234.6Kg, sodium pyrosulfate 1.46% 29.2Kg, ionic emulsifying agent 0.29% 5.8Kg, solubility promoter 0.29% 5.8Kg, cresols 0.29% 5.8Kg
Making method is as follows:
1) above-mentioned raw materials is put into stirred pot together by weight feeding to be uniformly mixed;
2) compound stirred is put into reactor and be heated to 350 DEG C;
3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000Kg
3hydrogen, then be down to normal temperature by tubulation device;
4) compound being down to normal temperature sends into finished pot, by 5% of total amount add ferrocene and 10% octane value for biological synthol.
In above-mentioned making processes, method 1) in churning time be 10 minutes, method formula) in heating after press and exhaustedly reach 4 pressure.
The various equipment that the present invention uses in making processes all can adopt traditional chemical industry equipment to produce, involved back-pressure still, and autoclave should be adopted to be good.
Claims (4)
1. a biosynthesizing fuel, comprises the methyl alcohol, ethanol, Viscotrol C and the sodium pyrosulfate that use in synthol, it is characterized in that:
Its formulation weight per-cent is as follows:
2. a making method for biosynthesizing fuel according to claim 1, its feature is being: described method point following steps are carried out:
1) above-mentioned raw materials is put into stirred pot together by weight feeding to be uniformly mixed;
2) compound stirred is put into reactor and be heated to 350 DEG C;
3) compound after heating is got rid of gas through gas-liquid separator, liquid directly enters catalytic tower, then injects 4m by every 1000kg
3hydrogen, then be down to normal temperature by tubulation device;
4) compound being down to normal temperature sends into finished pot, by 5% of total amount add ferrocene and 10% octane value for biological synthol.
3. the making method of biosynthesizing fuel according to claim 2, its feature is being: making method 1) in the time of stirring be 5 ~ 10 minutes.
4. the making method of biosynthesizing fuel according to claim 2, its feature is being: making method 2) in be heated to 350 DEG C, its air pressure should reach 4 pressure.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110271789.0A CN103131481B (en) | 2011-11-22 | 2011-11-22 | A kind of biosynthesizing fuel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201110271789.0A CN103131481B (en) | 2011-11-22 | 2011-11-22 | A kind of biosynthesizing fuel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103131481A CN103131481A (en) | 2013-06-05 |
| CN103131481B true CN103131481B (en) | 2016-03-30 |
Family
ID=48491941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201110271789.0A Active CN103131481B (en) | 2011-11-22 | 2011-11-22 | A kind of biosynthesizing fuel |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN103131481B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107629823A (en) * | 2016-07-18 | 2018-01-26 | 任卫国 | A kind of environmentally friendly synthetic liquid fuel |
| CN108070411A (en) * | 2016-11-18 | 2018-05-25 | 黄运国 | A kind of novel energy-saving environment-friendly fuel |
| CN113186005A (en) * | 2021-03-29 | 2021-07-30 | 叁久国际新能源科技有限公司 | Civil energy-saving environment-friendly fuel and preparation method thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1928035A (en) * | 2006-10-23 | 2007-03-14 | 姜彬 | Environmental protection energy-saving diesel oil |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007127059A2 (en) * | 2006-04-27 | 2007-11-08 | New Generation Biofuels, Inc. | Biofuel composition and method of producing a biofuel |
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2011
- 2011-11-22 CN CN201110271789.0A patent/CN103131481B/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1928035A (en) * | 2006-10-23 | 2007-03-14 | 姜彬 | Environmental protection energy-saving diesel oil |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103131481A (en) | 2013-06-05 |
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Application publication date: 20130605 Assignee: Cai Yongzong Assignor: Bai Fujun Contract record no.: X2022980017724 Denomination of invention: A kind of bio synthetic fuel Granted publication date: 20160330 License type: Exclusive License Record date: 20221011 |
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Application publication date: 20130605 Assignee: Cai Yongzong Assignor: Bai Fujun Contract record no.: X2023980042305 Denomination of invention: A Biosynthetic Fuel Granted publication date: 20160330 License type: Common License Record date: 20230926 |
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Application publication date: 20130605 Assignee: Xiangyang Fuzi Chemical Synthetic Fuel Co.,Ltd. Assignor: Bai Fujun Contract record no.: X2023980043349 Denomination of invention: A Biosynthetic Fuel Granted publication date: 20160330 License type: Common License Record date: 20231018 |
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