CN106573878A - 萃取蒸馏用的萃取溶剂以及使用所述溶剂的烃类的分离方法 - Google Patents
萃取蒸馏用的萃取溶剂以及使用所述溶剂的烃类的分离方法 Download PDFInfo
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- CN106573878A CN106573878A CN201580015895.9A CN201580015895A CN106573878A CN 106573878 A CN106573878 A CN 106573878A CN 201580015895 A CN201580015895 A CN 201580015895A CN 106573878 A CN106573878 A CN 106573878A
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- hydrocarbon
- propionic acid
- acid amide
- extractant
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- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000000605 extraction Methods 0.000 title claims description 25
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- 206010012438 Dermatitis atopic Diseases 0.000 description 1
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- HEQHXNXTDOAKMR-UHFFFAOYSA-N N,N-dibutyl-3-cyclohexyloxypropanamide Chemical compound C1(CCCCC1)OCCC(=O)N(CCCC)CCCC HEQHXNXTDOAKMR-UHFFFAOYSA-N 0.000 description 1
- JCYVYILSPGHYQN-UHFFFAOYSA-N N,N-dibutyl-3-pentoxypropanamide Chemical compound C(CCCC)OCCC(=O)N(CCCC)CCCC JCYVYILSPGHYQN-UHFFFAOYSA-N 0.000 description 1
- SUSLZQLPNPVBIT-UHFFFAOYSA-N N,N-diheptyl-3-pentoxypropanamide Chemical compound C(CCCC)OCCC(=O)N(CCCCCCC)CCCCCCC SUSLZQLPNPVBIT-UHFFFAOYSA-N 0.000 description 1
- YAPSCCVJGKOBRL-UHFFFAOYSA-N N,N-dihexyl-3-pentoxypropanamide Chemical compound CCCCCCN(CCCCCC)C(=O)CCOCCCCC YAPSCCVJGKOBRL-UHFFFAOYSA-N 0.000 description 1
- LCEDQNDDFOCWGG-UHFFFAOYSA-N N-Formyl-Morpholine Natural products O=CN1CCOCC1 LCEDQNDDFOCWGG-UHFFFAOYSA-N 0.000 description 1
- 101800000021 N-terminal protease Proteins 0.000 description 1
- 206010059516 Skin toxicity Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- BTGRAWJCKBQKAO-UHFFFAOYSA-N adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 description 1
- 201000008937 atopic dermatitis Diseases 0.000 description 1
- 238000000998 batch distillation Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- LMGZGXSXHCMSAA-UHFFFAOYSA-N cyclodecane Chemical compound C1CCCCCCCCC1 LMGZGXSXHCMSAA-UHFFFAOYSA-N 0.000 description 1
- UCIYGNATMHQYCT-OWOJBTEDSA-N cyclodecene Chemical compound C1CCCC\C=C\CCC1 UCIYGNATMHQYCT-OWOJBTEDSA-N 0.000 description 1
- DDTBPAQBQHZRDW-UHFFFAOYSA-N cyclododecane Chemical compound C1CCCCCCCCCCC1 DDTBPAQBQHZRDW-UHFFFAOYSA-N 0.000 description 1
- HYPABJGVBDSCIT-UPHRSURJSA-N cyclododecene Chemical compound C1CCCCC\C=C/CCCC1 HYPABJGVBDSCIT-UPHRSURJSA-N 0.000 description 1
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexediene Natural products C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 1
- 239000004913 cyclooctene Substances 0.000 description 1
- 150000001941 cyclopentenes Chemical class 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
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- 231100000025 genetic toxicology Toxicity 0.000 description 1
- 230000001738 genotoxic effect Effects 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- ZUBZATZOEPUUQF-UHFFFAOYSA-N isononane Chemical class CCCCCCC(C)C ZUBZATZOEPUUQF-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 231100000647 material safety data sheet Toxicity 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VQAXAEVAHOSPMQ-UHFFFAOYSA-N n,n-dimethyl-3-[(2-methylpropan-2-yl)oxy]propanamide Chemical class CN(C)C(=O)CCOC(C)(C)C VQAXAEVAHOSPMQ-UHFFFAOYSA-N 0.000 description 1
- FSSVZLVSRAFLGJ-UHFFFAOYSA-N n,n-dimethyl-3-pentoxypropanamide Chemical class CCCCCOCCC(=O)N(C)C FSSVZLVSRAFLGJ-UHFFFAOYSA-N 0.000 description 1
- ZIJQOYKHWORKOW-UHFFFAOYSA-N n,n-dimethyl-3-propan-2-yloxypropanamide Chemical class CC(C)OCCC(=O)N(C)C ZIJQOYKHWORKOW-UHFFFAOYSA-N 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- ABMDIECEEGFXNC-UHFFFAOYSA-N n-ethylpropanamide Chemical compound CCNC(=O)CC ABMDIECEEGFXNC-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl 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])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- IPYAJHHTWHZLJI-UHFFFAOYSA-N n-methyl-n-propylpropanamide Chemical compound CCCN(C)C(=O)CC IPYAJHHTWHZLJI-UHFFFAOYSA-N 0.000 description 1
- YUMCRXLLWKQDJY-UHFFFAOYSA-N n-propylpropanamide Chemical compound CCCNC(=O)CC YUMCRXLLWKQDJY-UHFFFAOYSA-N 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical class CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N pentadiene group Chemical class C=CC=CC PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
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- 238000011069 regeneration method Methods 0.000 description 1
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- 238000001577 simple distillation Methods 0.000 description 1
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- 125000001424 substituent group Chemical group 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- JXPOLSKBTUYKJB-UHFFFAOYSA-N xi-2,3-Dimethylhexane Chemical class CCCC(C)C(C)C JXPOLSKBTUYKJB-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/04—Purification; Separation; Use of additives by distillation
- C07C7/05—Purification; Separation; Use of additives by distillation with the aid of auxiliary compounds
- C07C7/08—Purification; Separation; Use of additives by distillation with the aid of auxiliary compounds by extractive distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014069968 | 2014-03-28 | ||
| JP2014-069968 | 2014-03-28 | ||
| PCT/JP2015/059103 WO2015147046A1 (fr) | 2014-03-28 | 2015-03-25 | Solvant d'extraction pour la distillation extractive et procédé de séparation d'hydrocarbures l'utilisant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106573878A true CN106573878A (zh) | 2017-04-19 |
Family
ID=54195557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201580015895.9A Pending CN106573878A (zh) | 2014-03-28 | 2015-03-25 | 萃取蒸馏用的萃取溶剂以及使用所述溶剂的烃类的分离方法 |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPWO2015147046A1 (fr) |
| CN (1) | CN106573878A (fr) |
| TW (1) | TW201600497A (fr) |
| WO (1) | WO2015147046A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112271400A (zh) * | 2020-09-01 | 2021-01-26 | 广州天赐高新材料股份有限公司 | 一种酰胺类化合物的新用途 |
| 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 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2023248810A1 (fr) * | 2022-06-24 | 2023-12-28 | 株式会社カネカ | Composition d'acide polyamique, procédé de production de polyimide, procédé de production de stratifié et procédé de production de dispositif électronique |
| WO2024190613A1 (fr) * | 2023-03-14 | 2024-09-19 | 株式会社カネカ | Composition de polyamide-acide, polyimide, film de polyimide, corps stratifié, dispositif électronique, procédé de production de polyimide, procédé de production d'un corps stratifié et procédé de production d'un dispositif électronique |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3914303A (en) * | 1972-09-01 | 1975-10-21 | Cpc International Inc | Preparation of N,N-dialkylacylamides |
| JP4377594B2 (ja) * | 2003-02-19 | 2009-12-02 | 出光興産株式会社 | β−アルコキシプロピオンアミド類の製造方法 |
| JP5601075B2 (ja) * | 2010-08-04 | 2014-10-08 | 株式会社リコー | インクジェット用インク、並びにインクカートリッジ、インクジェット記録方法、インクジェット記録装置及びインク記録物 |
| JP2013189411A (ja) * | 2012-03-15 | 2013-09-26 | Kohjin Holdings Co Ltd | Ｎ−置換−β−アルコキシプロピオン酸アミドの製造方法 |
-
2015
- 2015-03-25 WO PCT/JP2015/059103 patent/WO2015147046A1/fr active Application Filing
- 2015-03-25 JP JP2016510418A patent/JPWO2015147046A1/ja active Pending
- 2015-03-25 CN CN201580015895.9A patent/CN106573878A/zh active Pending
- 2015-03-26 TW TW104109759A patent/TW201600497A/zh unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112271400A (zh) * | 2020-09-01 | 2021-01-26 | 广州天赐高新材料股份有限公司 | 一种酰胺类化合物的新用途 |
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015147046A1 (fr) | 2015-10-01 |
| JPWO2015147046A1 (ja) | 2017-04-13 |
| TW201600497A (zh) | 2016-01-01 |
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| WD01 | Invention patent application deemed withdrawn after publication |