TWI432407B - 回收二氯丙醇之多階方法和裝置 - Google Patents
回收二氯丙醇之多階方法和裝置 Download PDFInfo
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- TWI432407B TWI432407B TW097113153A TW97113153A TWI432407B TW I432407 B TWI432407 B TW I432407B TW 097113153 A TW097113153 A TW 097113153A TW 97113153 A TW97113153 A TW 97113153A TW I432407 B TWI432407 B TW I432407B
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- Prior art keywords
- mixture
- boiling fraction
- dichloropropanol
- fraction
- ester
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- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
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- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
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- 235000019270 ammonium chloride Nutrition 0.000 description 1
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- 125000003710 aryl alkyl group Chemical group 0.000 description 1
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- 230000005540 biological transmission Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- PWLNAUNEAKQYLH-UHFFFAOYSA-N butyric acid octyl ester Natural products CCCCCCCCOC(=O)CCC PWLNAUNEAKQYLH-UHFFFAOYSA-N 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
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- 239000012018 catalyst precursor Substances 0.000 description 1
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- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- UYAAVKFHBMJOJZ-UHFFFAOYSA-N diimidazo[1,3-b:1',3'-e]pyrazine-5,10-dione Chemical compound O=C1C2=CN=CN2C(=O)C2=CN=CN12 UYAAVKFHBMJOJZ-UHFFFAOYSA-N 0.000 description 1
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- 238000000605 extraction Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
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- 150000002632 lipids Chemical class 0.000 description 1
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- 229940017219 methyl propionate Drugs 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 1
- HNBDRPTVWVGKBR-UHFFFAOYSA-N n-pentanoic acid methyl ester Natural products CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 150000002843 nonmetals Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
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- 239000003279 phenylacetic acid Substances 0.000 description 1
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- 229920000647 polyepoxide Polymers 0.000 description 1
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- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940116423 propylene glycol diacetate Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
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- 239000011347 resin Substances 0.000 description 1
- 238000007616 round robin method Methods 0.000 description 1
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 description 1
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- 150000003335 secondary amines Chemical class 0.000 description 1
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- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
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- 238000011144 upstream manufacturing Methods 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/80—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
- C07C29/82—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation by azeotropic distillation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
- B01D3/143—Fractional distillation or use of a fractionation or rectification column by two or more of a fractionation, separation or rectification step
- B01D3/146—Multiple effect distillation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/34—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
- B01D3/36—Azeotropic distillation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/34—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
- B01D3/38—Steam distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/34—Halogenated alcohols
- C07C31/36—Halogenated alcohols the halogen not being fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/34—Halogenated alcohols
- C07C31/42—Polyhydroxylic acyclic alcohols
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| US92310807P | 2007-04-12 | 2007-04-12 |
Publications (2)
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|---|---|
| TW200904786A TW200904786A (en) | 2009-02-01 |
| TWI432407B true TWI432407B (zh) | 2014-04-01 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW097113153A TWI432407B (zh) | 2007-04-12 | 2008-04-11 | 回收二氯丙醇之多階方法和裝置 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8664453B2 (enExample) |
| EP (1) | EP2137121A1 (enExample) |
| JP (1) | JP2010523698A (enExample) |
| KR (1) | KR20100016452A (enExample) |
| CN (1) | CN101657403B (enExample) |
| TW (1) | TWI432407B (enExample) |
| WO (1) | WO2008128004A1 (enExample) |
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| TW201518267A (zh) * | 2007-04-12 | 2015-05-16 | Dow Global Technologies Llc | 用於二氯丙醇的共沸回收之方法與設備 |
| US8664453B2 (en) | 2007-04-12 | 2014-03-04 | Dow Global Technologies Inc. | Multi-stage process and apparatus for recovering dichlorohydrins |
| CN101657404B (zh) * | 2007-04-12 | 2013-11-06 | 陶氏环球技术公司 | 用于经由共馏回收二氯代醇的方法和设备 |
| WO2008128011A2 (en) * | 2007-04-12 | 2008-10-23 | Dow Global Technologies Inc. | Conversion of a multihydroxylated-aliphatic hydrocarbon or ester thereof to a chlorohydrin |
| US20110152580A1 (en) * | 2007-04-12 | 2011-06-23 | Hook Bruce D | Process and apparatus for vapor phase purification during hydrochlorination of multi-hydroxylated aliphatic hydrocarbon compounds |
| CN101998944B (zh) | 2008-04-09 | 2014-09-03 | 陶氏环球技术公司 | 用于回收二氯代醇的多级方法和设备 |
| WO2011000896A1 (en) | 2009-07-03 | 2011-01-06 | Akzo Nobel Chemicals International B.V. | Process for preparing dichlorohydrin |
| JP5226710B2 (ja) * | 2010-02-01 | 2013-07-03 | 三井造船株式会社 | 高粘度重合液中の揮発性物質回収装置 |
| JP5756183B2 (ja) * | 2010-12-10 | 2015-07-29 | ダウ グローバル テクノロジーズ エルエルシー | １，３−ジクロロ−２−プロパノールを２，２’−オキシビス（１−クロロプロパン）廃棄ストリームから単離するためにオレフィンを共沸添加剤として用いるための装置及び方法 |
| BR112013014210B1 (pt) | 2010-12-10 | 2019-12-10 | Angus Chemical | processo para usar um nitroalcano como arrastador |
| BR112013007478A2 (pt) | 2012-01-25 | 2016-07-19 | Asahi Kasei Chemicals Corp | método de separação de separar (a) e (b) |
| EP2708525A1 (en) * | 2012-09-12 | 2014-03-19 | Solvay SA | Process of stripping a liquid medium |
| CN104761433B (zh) * | 2015-04-01 | 2018-07-20 | 中国天辰工程有限公司 | 用于甘油法ech回收二氯丙醇及催化剂的设备和工艺 |
| US12186683B2 (en) * | 2019-01-25 | 2025-01-07 | Borealis Ag | Separating device for separating volatile compounds from a polymer reaction mixture |
| US12453931B2 (en) | 2021-04-02 | 2025-10-28 | Natural Extraction Systems, LLC | Compositions for low-temperature distillation of high-boiling-point molecules |
| WO2022212912A1 (en) * | 2021-04-02 | 2022-10-06 | Natural Extraction Systems, LLC | Products and methods related to the distillation of molecules from aerosols |
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| JPS60258171A (ja) * | 1984-06-04 | 1985-12-20 | Showa Denko Kk | エピクロルヒドリンの製造方法 |
| GB9602680D0 (en) * | 1996-02-09 | 1996-04-10 | Ici Plc | Distillation process |
| CZ20032346A3 (cs) | 2003-09-01 | 2005-04-13 | Spolek Pro Chemickou A Hutní Výrobu,A.S. | Způsob přípravy dichlorpropanolů z glycerinu |
| CN1982269B (zh) * | 2003-11-20 | 2011-03-16 | 索尔维公司 | 用于生产有机化合物的方法 |
| EP1770081A1 (en) * | 2003-11-20 | 2007-04-04 | SOLVAY (Société Anonyme) | Process for producing dichloropropanol from glycerol , the glycerol coming eventualy from the conversion of animal fats in the manufacture of biodiesel |
| ATE454370T1 (de) | 2004-07-21 | 2010-01-15 | Dow Global Technologies Inc | Umwandlung eines mehrfach hydroxylierten aliphatischen kohlenwasserstoffes oder esters daraus in ein chlorhydrin |
| EP1762556A1 (en) * | 2005-05-20 | 2007-03-14 | SOLVAY (Société Anonyme) | Process for producing dichloropropanol from glycerol |
| US20080214848A1 (en) * | 2005-05-20 | 2008-09-04 | Solvay (Societe Anonyme) | Method For Making an Epoxy Starting From a Chlorhydrine |
| CN101657404B (zh) * | 2007-04-12 | 2013-11-06 | 陶氏环球技术公司 | 用于经由共馏回收二氯代醇的方法和设备 |
| US8664453B2 (en) | 2007-04-12 | 2014-03-04 | Dow Global Technologies Inc. | Multi-stage process and apparatus for recovering dichlorohydrins |
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2008
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- 2008-04-11 TW TW097113153A patent/TWI432407B/zh active
- 2008-04-11 JP JP2010503218A patent/JP2010523698A/ja active Pending
- 2008-04-11 CN CN200880011724.9A patent/CN101657403B/zh not_active Expired - Fee Related
- 2008-04-11 KR KR1020097023548A patent/KR20100016452A/ko not_active Ceased
- 2008-04-11 EP EP08745555A patent/EP2137121A1/en not_active Withdrawn
- 2008-04-11 WO PCT/US2008/059968 patent/WO2008128004A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| CN101657403A (zh) | 2010-02-24 |
| WO2008128004A1 (en) | 2008-10-23 |
| TW200904786A (en) | 2009-02-01 |
| KR20100016452A (ko) | 2010-02-12 |
| JP2010523698A (ja) | 2010-07-15 |
| EP2137121A1 (en) | 2009-12-30 |
| US8664453B2 (en) | 2014-03-04 |
| US20100137652A1 (en) | 2010-06-03 |
| CN101657403B (zh) | 2014-07-30 |
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