CN106831521A - 一种甲苯液相空气氧化法制备苄基过氧化物的方法 - Google Patents
一种甲苯液相空气氧化法制备苄基过氧化物的方法 Download PDFInfo
- Publication number
- CN106831521A CN106831521A CN201710130738.3A CN201710130738A CN106831521A CN 106831521 A CN106831521 A CN 106831521A CN 201710130738 A CN201710130738 A CN 201710130738A CN 106831521 A CN106831521 A CN 106831521A
- Authority
- CN
- China
- Prior art keywords
- toluene
- reaction
- oxidation
- high temperature
- catalyst
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 title claims abstract description 393
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 90
- 230000003647 oxidation Effects 0.000 title claims abstract description 71
- KQNZLOUWXSAZGD-UHFFFAOYSA-N benzylperoxymethylbenzene Chemical compound C=1C=CC=CC=1COOCC1=CC=CC=C1 KQNZLOUWXSAZGD-UHFFFAOYSA-N 0.000 title claims abstract description 41
- 238000000034 method Methods 0.000 title claims abstract description 39
- 239000007791 liquid phase Substances 0.000 title claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims abstract description 78
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000007789 gas Substances 0.000 claims abstract description 44
- 239000003054 catalyst Substances 0.000 claims abstract description 43
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 27
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 25
- 239000003999 initiator Substances 0.000 claims abstract description 23
- 239000002994 raw material Substances 0.000 claims abstract description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000001301 oxygen Substances 0.000 claims abstract description 20
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000007788 liquid Substances 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 20
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 claims description 7
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 claims description 7
- 238000001914 filtration Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000003860 storage Methods 0.000 claims description 6
- 238000011282 treatment Methods 0.000 claims description 6
- GAYAMOAYBXKUII-UHFFFAOYSA-L cobalt(2+);dibenzoate Chemical compound [Co+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 GAYAMOAYBXKUII-UHFFFAOYSA-L 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 4
- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- 238000000605 extraction Methods 0.000 claims description 3
- 229940011182 cobalt acetate Drugs 0.000 claims description 2
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- -1 benzyl ester Chemical class 0.000 abstract description 17
- 238000004519 manufacturing process Methods 0.000 abstract description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000460 chlorine Substances 0.000 abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 abstract description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 2
- 150000003934 aromatic aldehydes Chemical class 0.000 abstract description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract description 2
- 238000001816 cooling Methods 0.000 abstract description 2
- 230000007613 environmental effect Effects 0.000 abstract description 2
- 230000001276 controlling effect Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical group OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 5
- PVSCLHDHWOAWGV-UHFFFAOYSA-N oxygen;toluene Chemical compound [O].CC1=CC=CC=C1 PVSCLHDHWOAWGV-UHFFFAOYSA-N 0.000 description 4
- SVMCDCBHSKARBQ-UHFFFAOYSA-N acetic acid;cobalt Chemical compound [Co].CC(O)=O SVMCDCBHSKARBQ-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 235000013599 spices Nutrition 0.000 description 2
- JJJOZVFVARQUJV-UHFFFAOYSA-N 2-ethylhexylphosphonic acid Chemical compound CCCCC(CC)CP(O)(O)=O JJJOZVFVARQUJV-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- KGYGBOORGRYDGQ-UHFFFAOYSA-N benzene;methanol Chemical compound OC.C1=CC=CC=C1 KGYGBOORGRYDGQ-UHFFFAOYSA-N 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical group 0.000 description 1
- KLCQXXAKURQDOV-UHFFFAOYSA-N chlorobenzene methanol Chemical compound CO.CO.ClC1=CC=CC=C1 KLCQXXAKURQDOV-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/70—Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (7)
Priority Applications (1)
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CN201710130738.3A CN106831521B (zh) | 2017-03-07 | 2017-03-07 | 一种甲苯液相空气氧化法制备苄基过氧化物的方法 |
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CN201710130738.3A CN106831521B (zh) | 2017-03-07 | 2017-03-07 | 一种甲苯液相空气氧化法制备苄基过氧化物的方法 |
Publications (2)
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CN106831521A true CN106831521A (zh) | 2017-06-13 |
CN106831521B CN106831521B (zh) | 2018-08-21 |
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CN201710130738.3A Active CN106831521B (zh) | 2017-03-07 | 2017-03-07 | 一种甲苯液相空气氧化法制备苄基过氧化物的方法 |
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2683751A (en) * | 1950-10-31 | 1954-07-13 | Hercules Powder Co Ltd | Phenol production |
US3387036A (en) * | 1963-05-22 | 1968-06-04 | Rhone Poulenc Sa | Production of benzyl alcohol and benzaldehyde |
CN1035960A (zh) * | 1988-09-16 | 1989-10-04 | 肖藻生 | 一种烃类氧化的络合催化剂 |
CN1530358A (zh) * | 2003-01-24 | 2004-09-22 | 中国石油化工股份有限公司巴陵分公司 | 催化氧化环己烷工艺 |
CN1670130A (zh) * | 2004-03-16 | 2005-09-21 | 中国科学院大连化学物理研究所 | 一种用于烃类催化选择氧化的非金属复合催化体系 |
CN102115353A (zh) * | 2009-12-30 | 2011-07-06 | 中国科学院大连化学物理研究所 | 一种芳烃选择性氧化的方法 |
CN104418782A (zh) * | 2013-09-10 | 2015-03-18 | 中国石油化工集团公司 | 通过二异丙苯氧化制备氢过氧化物混合物的方法 |
CN105523982A (zh) * | 2014-10-23 | 2016-04-27 | 茅海强 | 一种叔丁基过氧化氢的制备方法 |
-
2017
- 2017-03-07 CN CN201710130738.3A patent/CN106831521B/zh active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2683751A (en) * | 1950-10-31 | 1954-07-13 | Hercules Powder Co Ltd | Phenol production |
US3387036A (en) * | 1963-05-22 | 1968-06-04 | Rhone Poulenc Sa | Production of benzyl alcohol and benzaldehyde |
CN1035960A (zh) * | 1988-09-16 | 1989-10-04 | 肖藻生 | 一种烃类氧化的络合催化剂 |
CN1530358A (zh) * | 2003-01-24 | 2004-09-22 | 中国石油化工股份有限公司巴陵分公司 | 催化氧化环己烷工艺 |
CN1670130A (zh) * | 2004-03-16 | 2005-09-21 | 中国科学院大连化学物理研究所 | 一种用于烃类催化选择氧化的非金属复合催化体系 |
CN102115353A (zh) * | 2009-12-30 | 2011-07-06 | 中国科学院大连化学物理研究所 | 一种芳烃选择性氧化的方法 |
CN104418782A (zh) * | 2013-09-10 | 2015-03-18 | 中国石油化工集团公司 | 通过二异丙苯氧化制备氢过氧化物混合物的方法 |
CN105523982A (zh) * | 2014-10-23 | 2016-04-27 | 茅海强 | 一种叔丁基过氧化氢的制备方法 |
Non-Patent Citations (4)
Title |
---|
G.DOBSON ET AL.: "The Radiation-Induced Oxidation of Organic Compounds", 《G.DOBSON AND G.HUGHE》 * |
唐盛伟: "甲苯液相空气氧化反应过程研究", 《中国优秀博硕士学位论文全文数据库(博士)工程科技I辑》 * |
唐盛伟等: "甲苯液相氧化反应过程的动力学研究", 《化学反应工程与工艺》 * |
程婧等: "甲苯液相均相选择性催化氧化研究进展", 《化学工业与工程》 * |
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CN106831521B (zh) | 2018-08-21 |
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Denomination of invention: A method for preparing benzyl peroxide by liquid phase air oxidation of toluene Effective date of registration: 20220111 Granted publication date: 20180821 Pledgee: Agricultural Bank of China Limited Zhijiang sub branch Pledgor: HUBEI KELIN BOLUN NEW MATERIAL CO.,LTD. Registration number: Y2022980000347 |
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Date of cancellation: 20231215 Granted publication date: 20180821 Pledgee: Agricultural Bank of China Limited Zhijiang sub branch Pledgor: HUBEI KELIN BOLUN NEW MATERIAL CO.,LTD. Registration number: Y2022980000347 |
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Denomination of invention: A method for preparing benzyl peroxide by liquid-phase air oxidation of toluene Effective date of registration: 20231227 Granted publication date: 20180821 Pledgee: Agricultural Bank of China Limited Zhijiang sub branch Pledgor: HUBEI KELIN BOLUN NEW MATERIAL CO.,LTD. Registration number: Y2023980074318 |
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