CN107057746B - 一种利用聚3-羟基丁酸酯制备液体燃料的方法 - Google Patents
一种利用聚3-羟基丁酸酯制备液体燃料的方法 Download PDFInfo
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- CN107057746B CN107057746B CN201710325047.9A CN201710325047A CN107057746B CN 107057746 B CN107057746 B CN 107057746B CN 201710325047 A CN201710325047 A CN 201710325047A CN 107057746 B CN107057746 B CN 107057746B
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- China
- Prior art keywords
- poly
- liquid fuel
- hydroxy butyrate
- dihydrogen phosphate
- catalyst
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- 239000007788 liquid Substances 0.000 title claims abstract description 26
- 239000000446 fuel Substances 0.000 title claims abstract description 24
- 238000000034 method Methods 0.000 title claims abstract description 15
- 229920000070 poly-3-hydroxybutyrate Polymers 0.000 title claims description 35
- 239000003054 catalyst Substances 0.000 claims abstract description 34
- 238000006243 chemical reaction Methods 0.000 claims abstract description 30
- RGPUVZXXZFNFBF-UHFFFAOYSA-K diphosphonooxyalumanyl dihydrogen phosphate Chemical compound [Al+3].OP(O)([O-])=O.OP(O)([O-])=O.OP(O)([O-])=O RGPUVZXXZFNFBF-UHFFFAOYSA-K 0.000 claims abstract description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 238000010792 warming Methods 0.000 claims description 2
- 230000007717 exclusion Effects 0.000 claims 1
- 238000006114 decarboxylation reaction Methods 0.000 abstract description 9
- 230000003197 catalytic effect Effects 0.000 abstract description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 3
- 229910052799 carbon Inorganic materials 0.000 abstract description 3
- 229930195733 hydrocarbon Natural products 0.000 abstract description 3
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- OBNCKNCVKJNDBV-UHFFFAOYSA-N ethyl butyrate Chemical compound CCCC(=O)OCC OBNCKNCVKJNDBV-UHFFFAOYSA-N 0.000 abstract 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 6
- -1 3-hydroxybutyrate ester Chemical class 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 238000002329 infrared spectrum Methods 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical group C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000000197 pyrolysis Methods 0.000 description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WHBMMWSBFZVSSR-UHFFFAOYSA-N R3HBA Natural products CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229920002800 poly crotonic acid Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- 239000002028 Biomass Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007707 calorimetry Methods 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000513 principal component analysis Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
Landscapes
- Chemical & Material Sciences (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201710325047.9A CN107057746B (zh) | 2017-05-10 | 2017-05-10 | 一种利用聚3-羟基丁酸酯制备液体燃料的方法 |
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CN201710325047.9A CN107057746B (zh) | 2017-05-10 | 2017-05-10 | 一种利用聚3-羟基丁酸酯制备液体燃料的方法 |
Publications (2)
Publication Number | Publication Date |
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CN107057746A CN107057746A (zh) | 2017-08-18 |
CN107057746B true CN107057746B (zh) | 2018-09-04 |
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CN201710325047.9A Active CN107057746B (zh) | 2017-05-10 | 2017-05-10 | 一种利用聚3-羟基丁酸酯制备液体燃料的方法 |
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CN (1) | CN107057746B (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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CN108383675B (zh) * | 2018-03-09 | 2021-02-23 | 东莞理工学院 | 一种聚3-羟基丁酸酯制备丙烯的催化转化方法 |
CN111961507A (zh) * | 2020-08-31 | 2020-11-20 | 东莞理工学院 | 一种聚ε-己内酯制备低分子醇类和酯类液体的方法 |
CN111973929B (zh) * | 2020-08-31 | 2021-11-02 | 济南磐升生物技术有限公司 | 一种无溶剂催化降解聚乳酸的方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4363748A (en) * | 1982-02-02 | 1982-12-14 | El Paso Products Company | Catalyst composition for producing tertiary-butylstyrene |
CN1246853A (zh) * | 1997-02-07 | 2000-03-08 | 国际壳牌研究有限公司 | 制备环氧化合物的方法 |
CN101811059A (zh) * | 2010-04-14 | 2010-08-25 | 太原理工大学 | 一种乳酸酯催化脱水催化剂及其制备和应用 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6133180A (ja) * | 1984-07-24 | 1986-02-17 | Daicel Chem Ind Ltd | エポキシ化合物の製造方法 |
-
2017
- 2017-05-10 CN CN201710325047.9A patent/CN107057746B/zh active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4363748A (en) * | 1982-02-02 | 1982-12-14 | El Paso Products Company | Catalyst composition for producing tertiary-butylstyrene |
CN1246853A (zh) * | 1997-02-07 | 2000-03-08 | 国际壳牌研究有限公司 | 制备环氧化合物的方法 |
CN101811059A (zh) * | 2010-04-14 | 2010-08-25 | 太原理工大学 | 一种乳酸酯催化脱水催化剂及其制备和应用 |
Non-Patent Citations (3)
Title |
---|
A gasoline-grade biofuel formed from renewable polyhydroxybutyrate on solid phosphoric acid;Kang, SM;《Fuel》;20151115;第160卷;第2.5.1节、第4节 * |
One-pot production of hydrocarbon oil from poly(3-hydroxybutyrate);Kang, Shimin;《RSC Advances》;20140507;第4卷(第28期);第14320-14327页 * |
Reaction routes in catalytic reforming of poly(3-hydroxybutyrate) into renewable hydrocarbon oil;Kang, SM;《RSC ADVANCES》;20150512;第5卷(第38期);第30005-30013页 * |
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CN107057746A (zh) | 2017-08-18 |
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Application publication date: 20170818 Assignee: Dongguan Creative Environmental New Materials Technology Co.,Ltd. Assignor: DONGGUAN University OF TECHNOLOGY Contract record no.: X2022980027689 Denomination of invention: A method for preparing liquid fuel from poly (3-hydroxybutyrate) Granted publication date: 20180904 License type: Common License Record date: 20221230 |
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Effective date of registration: 20240521 Address after: Room 413, 4th Floor, Building 1, Courtyard 1, Wanxing Road, Fengtai District, Beijing, 100000 Patentee after: Shuiranbao (Beijing) New Energy Co.,Ltd. Country or region after: China Address before: 523000, 1, University Road, Songshan science and Technology Industrial Park, Guangdong, Dongguan Patentee before: DONGGUAN University OF TECHNOLOGY Country or region before: China |