CN1683309A - 萃取与共沸精馏相结合提纯(甲基)丙烯酸的工艺方法 - Google Patents
萃取与共沸精馏相结合提纯(甲基)丙烯酸的工艺方法 Download PDFInfo
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- CN1683309A CN1683309A CN 200510013188 CN200510013188A CN1683309A CN 1683309 A CN1683309 A CN 1683309A CN 200510013188 CN200510013188 CN 200510013188 CN 200510013188 A CN200510013188 A CN 200510013188A CN 1683309 A CN1683309 A CN 1683309A
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- 238000000034 method Methods 0.000 title claims abstract description 50
- 230000008569 process Effects 0.000 title claims abstract description 46
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 title claims abstract description 24
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 144
- 238000000605 extraction Methods 0.000 claims abstract description 81
- 239000002904 solvent Substances 0.000 claims abstract description 79
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 69
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000000746 purification Methods 0.000 claims abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 5
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- 230000018044 dehydration Effects 0.000 claims description 39
- 238000006297 dehydration reaction Methods 0.000 claims description 39
- 241000282326 Felis catus Species 0.000 claims description 32
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 28
- 239000007864 aqueous solution Substances 0.000 claims description 25
- LDHQCZJRKDOVOX-UHFFFAOYSA-N 2-butenoic acid Chemical compound CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 22
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 15
- 238000003672 processing method Methods 0.000 claims description 15
- 238000010533 azeotropic distillation Methods 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 238000011084 recovery Methods 0.000 claims description 9
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 8
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 8
- 239000002351 wastewater Substances 0.000 claims description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 claims description 4
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
- IFTRQJLVEBNKJK-UHFFFAOYSA-N Ethylcyclopentane Chemical compound CCC1CCCC1 IFTRQJLVEBNKJK-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 claims description 4
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 claims description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 claims description 4
- 239000000243 solution Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 3
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 claims description 3
- 238000010926 purge Methods 0.000 claims description 3
- 230000008439 repair process Effects 0.000 claims description 3
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims description 2
- MLRVZFYXUZQSRU-UHFFFAOYSA-N 1-chlorohexane Chemical compound CCCCCCCl MLRVZFYXUZQSRU-UHFFFAOYSA-N 0.000 claims description 2
- SQCZQTSHSZLZIQ-UHFFFAOYSA-N 1-chloropentane Chemical compound CCCCCCl SQCZQTSHSZLZIQ-UHFFFAOYSA-N 0.000 claims description 2
- RQUBQBFVDOLUKC-UHFFFAOYSA-N 1-ethoxy-2-methylpropane Chemical compound CCOCC(C)C RQUBQBFVDOLUKC-UHFFFAOYSA-N 0.000 claims description 2
- PZHIWRCQKBBTOW-UHFFFAOYSA-N 1-ethoxybutane Chemical compound CCCCOCC PZHIWRCQKBBTOW-UHFFFAOYSA-N 0.000 claims description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims description 2
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 239000008346 aqueous phase Substances 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- 150000001924 cycloalkanes Chemical class 0.000 claims description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 2
- QPJORFLSOJAUNL-UHFFFAOYSA-N dibenzo[a,d][7]annulene Chemical compound C1=CC2=CC=CC=C2CC2=CC=CC=C21 QPJORFLSOJAUNL-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 150000005826 halohydrocarbons Chemical class 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- WSGCRAOTEDLMFQ-UHFFFAOYSA-N nonan-5-one Chemical compound CCCCC(=O)CCCC WSGCRAOTEDLMFQ-UHFFFAOYSA-N 0.000 claims description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- -1 propyl group ketone Chemical class 0.000 claims description 2
- 210000000689 upper leg Anatomy 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 238000007670 refining Methods 0.000 abstract description 3
- 230000008030 elimination Effects 0.000 abstract 2
- 238000003379 elimination reaction Methods 0.000 abstract 2
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- 238000002474 experimental method Methods 0.000 description 12
- 239000012074 organic phase Substances 0.000 description 10
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- 238000005265 energy consumption Methods 0.000 description 7
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- 238000001704 evaporation Methods 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000002131 composite material Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000010924 continuous production Methods 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 2
- IESCSIXIJXPWRJ-UHFFFAOYSA-N acetic acid;prop-2-enoic acid Chemical compound CC(O)=O.OC(=O)C=C.OC(=O)C=C IESCSIXIJXPWRJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000004134 energy conservation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 2
- USHYOWIBEFOXMB-UHFFFAOYSA-N toluene dihydrate Chemical compound C1(=CC=CC=C1)C.O.O USHYOWIBEFOXMB-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- BQFCCCIRTOLPEF-UHFFFAOYSA-N chembl1976978 Chemical compound CC1=CC=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 BQFCCCIRTOLPEF-UHFFFAOYSA-N 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical compound CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
顶温 | 釜温 | 塔釜组成% | 塔顶有机相组成% | 塔顶水相组成% |
℃ | ℃ | 水 | 甲苯 | 水 | 醋酸 | 丙烯酸 | 丙烯酸 |
40.3 | 82.5 | 0.05 | 99.4 | 0.1 | 0.2 | 0.3 | 0.43 |
组成 | 溶剂相% | 水相% |
水 | 0.55 | 99.22 |
醋酸 | 0.56 | 0.55 |
甲苯 | 88.51 | 0.08 |
丙烯酸 | 10.39 | 0.15 |
顶温 | 釜温 | 塔釜组成% | 塔顶有机相组成% | 塔顶水相组成% | |||
℃ | ℃ | 水 | 甲苯 | 水 | 醋酸 | 丙烯酸 | 丙烯酸 |
40.3 | 82.5 | 0.05 | 99.4 | 0.08 | 0.2 | 0.3 | 0.42 |
Claims (10)
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CNB2005100131884A CN1304354C (zh) | 2005-02-06 | 2005-02-06 | 萃取与共沸精馏相结合提纯(甲基)丙烯酸的工艺方法 |
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CNB2005100131884A CN1304354C (zh) | 2005-02-06 | 2005-02-06 | 萃取与共沸精馏相结合提纯(甲基)丙烯酸的工艺方法 |
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Publication Number | Publication Date |
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CN1683309A true CN1683309A (zh) | 2005-10-19 |
CN1304354C CN1304354C (zh) | 2007-03-14 |
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CNB2005100131884A Active CN1304354C (zh) | 2005-02-06 | 2005-02-06 | 萃取与共沸精馏相结合提纯(甲基)丙烯酸的工艺方法 |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101835736A (zh) * | 2007-10-23 | 2010-09-15 | Lg化学株式会社 | 收集(甲基)丙烯酸的方法和收集(甲基)丙烯酸的装置 |
CN105399620A (zh) * | 2015-11-13 | 2016-03-16 | 惠州市长润发涂料有限公司 | 一种丙烯酸萃取回收技术 |
CN108430965A (zh) * | 2015-12-25 | 2018-08-21 | 三菱化学株式会社 | (甲基)丙烯酸的制造方法 |
CN108884013A (zh) * | 2016-11-25 | 2018-11-23 | 株式会社Lg化学 | 连续回收(甲基)丙烯酸的方法和用于该方法的装置 |
CN109071401A (zh) * | 2016-12-06 | 2018-12-21 | 株式会社Lg化学 | (甲基)丙烯酸的回收方法 |
CN112374676A (zh) * | 2020-10-22 | 2021-02-19 | 江苏扬农化工集团有限公司 | 一种环氧氯丙烷废水中副产物分离提纯的装置及方法 |
CN114751826A (zh) * | 2022-04-21 | 2022-07-15 | 厦门大学 | 一种分离乙酸乙酯和甲基环己烷恒沸物的萃取精馏方法 |
CN115448834A (zh) * | 2022-09-16 | 2022-12-09 | 卫星化学股份有限公司 | 一种丙烯酸水溶液精制的方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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FR2736912B1 (fr) * | 1995-07-18 | 1997-08-22 | Atochem Elf Sa | Procede de purification de l'acide acrylique obtenu par oxydation catalytique du propylene |
JP3028925B2 (ja) * | 1995-12-05 | 2000-04-04 | 株式会社日本触媒 | アクリル酸の製造方法 |
CN1241892C (zh) * | 2003-12-09 | 2006-02-15 | 上海华谊丙烯酸有限公司 | 一种纯化丙烯酸的方法 |
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2005
- 2005-02-06 CN CNB2005100131884A patent/CN1304354C/zh active Active
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CN105399620A (zh) * | 2015-11-13 | 2016-03-16 | 惠州市长润发涂料有限公司 | 一种丙烯酸萃取回收技术 |
CN108430965B (zh) * | 2015-12-25 | 2021-03-16 | 三菱化学株式会社 | (甲基)丙烯酸的制造方法 |
CN108430965A (zh) * | 2015-12-25 | 2018-08-21 | 三菱化学株式会社 | (甲基)丙烯酸的制造方法 |
US11034642B2 (en) | 2016-11-25 | 2021-06-15 | Lg Chem, Ltd. | Method and apparatus for continuously recovering (meth)acrylic acid |
CN108884013B (zh) * | 2016-11-25 | 2021-02-12 | 株式会社Lg化学 | 连续回收(甲基)丙烯酸的方法和用于该方法的装置 |
CN108884013A (zh) * | 2016-11-25 | 2018-11-23 | 株式会社Lg化学 | 连续回收(甲基)丙烯酸的方法和用于该方法的装置 |
CN109071401A (zh) * | 2016-12-06 | 2018-12-21 | 株式会社Lg化学 | (甲基)丙烯酸的回收方法 |
CN109071401B (zh) * | 2016-12-06 | 2021-04-02 | 株式会社Lg化学 | (甲基)丙烯酸的回收方法 |
CN112374676A (zh) * | 2020-10-22 | 2021-02-19 | 江苏扬农化工集团有限公司 | 一种环氧氯丙烷废水中副产物分离提纯的装置及方法 |
CN112374676B (zh) * | 2020-10-22 | 2023-07-04 | 江苏扬农化工集团有限公司 | 一种环氧氯丙烷废水中副产物分离提纯的装置及方法 |
CN114751826A (zh) * | 2022-04-21 | 2022-07-15 | 厦门大学 | 一种分离乙酸乙酯和甲基环己烷恒沸物的萃取精馏方法 |
CN114751826B (zh) * | 2022-04-21 | 2023-02-28 | 厦门大学 | 一种分离乙酸乙酯和甲基环己烷恒沸物的萃取精馏方法 |
CN115448834A (zh) * | 2022-09-16 | 2022-12-09 | 卫星化学股份有限公司 | 一种丙烯酸水溶液精制的方法 |
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