KR960031412A - Method for producing isopropyl alcohol - Google Patents

Method for producing isopropyl alcohol Download PDF

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Publication number
KR960031412A
KR960031412A KR1019960004512A KR19960004512A KR960031412A KR 960031412 A KR960031412 A KR 960031412A KR 1019960004512 A KR1019960004512 A KR 1019960004512A KR 19960004512 A KR19960004512 A KR 19960004512A KR 960031412 A KR960031412 A KR 960031412A
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South Korea
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isopropyl alcohol
saturated hydrocarbon
extraction
liquid phase
reaction mixture
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KR1019960004512A
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Korean (ko)
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KR100219006B1 (en
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시게루 히라타
신지 오가오
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사토 아키오
미쯔이도오아쯔가가꾸 가부시기가이샤
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/03Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
    • C07C29/04Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/02Monohydroxylic acyclic alcohols
    • C07C31/10Monohydroxylic acyclic alcohols containing three carbon atoms

Abstract

강산성고체촉매존재하에, 프로필렌과 물을 고온, 고압하에서 직접액상수화하여 이소프로필알콜을 제조하는 방법에 있어서, 반응을 여분의 물을 공급하면서 60~200atm하 100~250℃에서 행하고, 반응을 통해 형성된 액상을 탄소수 3 또는 4의 포화탄화수소로 형성된 추출제와 함께 추출제의 임계온도~임계온도보다 40℃ 높은 온도 및 추출제의 임계입력~200atm하에서, 추출되는 원료량으로 나눈 추출제의 양으로 표현된 식에서 계산하여 0.3~3의 비율이 되도록 접촉하고, 마지막으로, 액상에서 이소프로필알콜을 추출한 후, 얻어진 추출상에서 분리한다. 이 방법에 의하면, 이소프로필알콜을 농축하기 위해 필요한 에너지가 감소되고, 대규모 제조설비를 필요로 하지 않는다.A process for producing isopropyl alcohol by directly hydrolyzing propylene and water under high pressure and high pressure in the presence of a strongly acidic solid catalyst, wherein the reaction is carried out at 60 to 200 atm at 100 to 250 ° C while supplying extra water, The liquid phase formed is divided into the amount of the extracting agent divided by the amount of the raw material extracted at a temperature higher than the critical temperature of the extracting agent by 40 ° C. and the critical input of the extracting agent to 200 atm together with the extraction agent formed of saturated hydrocarbons having 3 or 4 carbon atoms And is contacted so as to have a ratio of 0.3 to 3 calculated from the expression, and finally, isopropyl alcohol is extracted from the liquid phase and then separated on the obtained extraction. According to this method, the energy required to concentrate isopropyl alcohol is reduced and does not require a large-scale production facility.

Description

이소프로필알콜의 제조방법Method for producing isopropyl alcohol

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is a trivial issue, I did not include the contents of the text.

Claims (7)

강산성고체촉매존재하에, 프로필렌과 물을 고온, 고압하에서 직접 수화하고, 얻어진 반응혼합물에서 조이소프로필알콜용액분리하고, 이 용액을 정제하여 이소프로필알콜을 제조할때에, (1) 고체촉매를 충전 또는 현탁한 반응 기내에, 프로필렌과, 반응되는 프로필렌 1몰당 적어도 1몰 이상으로 되는 물을 연속적으로 공급하고, 100~250℃, 60~200atm에서 반응시키고, (2)반응혼합물의 기상과 액상 전량을 반응기로부터 연속추출하고, (3)반응혼합물의 기상을 증류탑에 공급하여, 탑바닥에서, 주로 원료프로필렌에 함유된 프로판으로 이루어지는 불순물을 제거하고, 탑상부에서 미반응프로필렌을 회수하여 반응기입구내로 재순환시키고, (4)상기 반응혼합물의 액상을, 탄소수 3또는 4의 포화탄화수소로 형성된 추출제와, 상기 추출제의 임계온도~임계온도보다 40℃높은 온도와, 상기 추출제의 임계압력~200atm에서, 원료의 추출되는 량으로 나눈 상기 추출제의 양으로 표현된 식으로 계산하여 0.3~3인 비율로 접촉시켜, 상기 반응혼합물의 액상으로부터, 반응을 통해 형성된 물질로서 이소프로필알콜을 추출하고, (5) 주로 물로 이루어진, 추출 후 남은 액체의 주요량을 재순환하고, (6) 주로 상기 포화탄화수소로 이루어진 추출상에서 이소프로필알콜을 고농도용액으로 분리하고, 이용액을 정제하여 정제된 이소프로필알콜을 얻는 공정으로 이루어진 것을 특징으로 하는 이소프로필알콜의 제조방법.In the presence of a strong acidic solid catalyst, propylene and water are directly hydrated at a high temperature and under a high pressure, and the resulting reaction mixture is separated into a jouisopropyl alcohol solution, and this solution is purified to prepare isopropyl alcohol. (1) (2) a step of continuously feeding propylene and water to be reacted at a rate of at least 1 mole per mole of propylene continuously at a temperature of 100 to 250 ° C and at a temperature of 60 to 200 atm in a packed or suspended reactor, (3) The gaseous phase of the reaction mixture is fed to the distillation column to remove impurities composed mainly of propane contained in the raw propylene at the bottom of the column, recover unreacted propylene from the top of the column, (4) contacting the liquid phase of the reaction mixture with an extraction agent formed of saturated hydrocarbons having 3 or 4 carbon atoms and an extraction agent formed of a saturated hydrocarbon having a carbon number of 40 From a liquid phase of the reaction mixture at a high temperature and a ratio of 0.3 to 3 as calculated by the expression expressed by the amount of the extracting agent divided by the extraction amount of the raw material at the critical pressure of the extracting agent to 200 atm, (5) recirculating a major amount of the remaining liquid after the extraction, which is mainly composed of water, and (6) separating isopropyl alcohol into a high concentration solution mainly on the extract consisting of the saturated hydrocarbons And a step of purifying the use liquid to obtain purified isopropyl alcohol. 제1항에 있어서, 상기 반응혼합물의 액상과 상기 추출제를 접촉시켜 얻은, 주로 상기 포화탄화수소로 이루어진 추출상에서, 반응을 통해 형성된 고농도 용액으로서 이소프로필알콜을, 주로 상기 포화탄화수소로 이루어진 기상과, 주로 이소프로필알콜과 물로 이루어진 액상으로, 추출상의 압력을 상기 포화탄화수소의 임계 압력 이하로 감소시킴으로서 분리하는 것을 특징으로 하는 이소프로필알콜의 제조방법.2. The method according to claim 1, wherein isopropyl alcohol as the high concentration solution formed through the reaction in the extraction phase mainly composed of the saturated hydrocarbon obtained by bringing the liquid phase of the reaction mixture into contact with the extraction agent is mixed with the vapor phase mainly composed of the saturated hydrocarbons, Characterized in that a liquid phase consisting mainly of isopropyl alcohol and water is separated by reducing the pressure of the extraction phase to below the critical pressure of the saturated hydrocarbon. 제1항에 있어서, 상기 반응혼합물의 액상과 상기 추출제를 접촉시켜 얻은, 주로 상기 포화탄화수소로 이루어진 추출상에서, 반응을 통해 형성된 고농도 용액으로서의 이소프로필알콜을, 주로 상기 포화탄화수소로 이루어진 가벼운 액상과, 주로 이소피로필알콜과 물로 이루어진 무거운 액상으로 실질적으로 추출상의 압력을 유지하면서, 상기 포화탄화수소의 임계 온도 이하로 추출상을 냉각시킴으로서 분리하는 것을 특징으로 하는 이소프로필알콜의 제조방법.2. The method according to claim 1, wherein isopropyl alcohol as a high concentration solution formed through the reaction in an extraction phase mainly composed of the saturated hydrocarbon obtained by bringing the liquid phase of the reaction mixture into contact with the extractant is mixed with a light liquid phase mainly composed of the saturated hydrocarbon Characterized in that the separation is carried out by cooling the extracted phase to below the critical temperature of the saturated hydrocarbon while maintaining the pressure of the extraction phase substantially in a heavy liquid phase consisting mainly of isopyropyl alcohol and water. 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 반응혼합물의 액상과 상기 추출제를 접촉시켜 얻은, 주로 상기 포화탄화수소로 이루어진 추출상에서, 반응을 통해 형성된 이소프로필알콜을 고농도 용액으로서 분리한 후에 회수된 상기 포화탄화수소의 주요량을 추출제로서 재순환시키는 공정을 포함하는 것을 특징으로 하는 이소프로필알콜의 제조방법.4. The method according to any one of claims 1 to 3, wherein isopropyl alcohol formed through the reaction is separated as a high-concentration solution, which is obtained by contacting the liquid phase of the reaction mixture with the extractant and mainly comprising the saturated hydrocarbon, And recycling the recovered major amount of the saturated hydrocarbon as an extractant. 제4항에 있어서, 상기 추출제로서 재순환사용하는 상기 포화탄화수소의 일부를 추출하여, 상기 반응혼합물의 기상과 함께 증기탑에 공급하고, 증류탑바닥에서 상기 포화탄화수소를 분리하는 것을 특징으로 하는 이소프로필알콜의 제조방법.5. The process according to claim 4, wherein part of the saturated hydrocarbon recycled as the extractant is extracted and fed to the vapor column together with the vapor phase of the reaction mixture, and the saturated hydrocarbon is separated from the bottom of the distillation tower. ≪ / RTI > 제1항 내지 제5항 중 어느 한 항에 있어서, 상기 포화탄화수소는 프로판인 것을 특징으로 하는 이소프로필알콜의 제조방법.6. The process for producing isopropyl alcohol according to any one of claims 1 to 5, wherein the saturated hydrocarbon is propane. 제1항 내지 제6항 중 어느 한 항에 있어서, 상기 추출제의 적어도 일부로서 원료프로필렌에 함유되어 있고, 미반응프로필렌의 증류회수시에 증류탑의 바닥에서 분리되는 프로판을 사용하는 것을 특징으로 하는 이소프로필알콜의 제조방법.7. A process according to any one of claims 1 to 6, characterized in that propane which is contained in the raw propylene as at least a part of the extracting agent and is separated from the bottom of the distillation column at the time of distillation recovery of unreacted propylene is used Isopropyl alcohol. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: It is disclosed by the contents of the first application.
KR1019960004512A 1995-02-24 1996-02-24 Process for producing isopropyl alcohol KR100219006B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP95-37136 1995-02-24
JP95-3136 1995-02-24
JP3713695 1995-02-24

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KR960031412A true KR960031412A (en) 1996-09-17
KR100219006B1 KR100219006B1 (en) 1999-09-01

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MY (1) MY112960A (en)
SG (1) SG50572A1 (en)
TW (1) TW338031B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014003475A1 (en) * 2012-06-28 2014-01-03 주식회사 엘지화학 Method for producing isopropyl alcohol

Families Citing this family (6)

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Publication number Priority date Publication date Assignee Title
JP7118898B2 (en) * 2017-01-23 2022-08-16 株式会社トクヤマ Isopropyl alcohol composition and method for producing isopropyl alcohol
KR102586512B1 (en) * 2020-06-23 2023-10-06 주식회사 엘지화학 Method for preraring isopropyl alcohol
KR20220151452A (en) * 2021-05-06 2022-11-15 주식회사 엘지화학 Method for preraring isopropyl alcohol
KR20220161920A (en) * 2021-05-31 2022-12-07 주식회사 엘지화학 Method for preraring isopropyl alcohol
KR20220161915A (en) * 2021-05-31 2022-12-07 주식회사 엘지화학 Method for preraring isopropyl alcohol
WO2024043443A1 (en) * 2022-08-22 2024-02-29 주식회사 엘지화학 Method for preparing isopropyl alcohol

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DE1249845B (en) * 1965-07-24
DE2429770C3 (en) * 1974-06-21 1981-04-16 Deutsche Texaco Ag, 2000 Hamburg Process for the production of lower alcohols by direct catalytic hydration of lower olefins
US4469903A (en) * 1983-09-21 1984-09-04 Uop Inc. Process for the production of isopropyl alcohol
JPS6225983A (en) * 1985-07-29 1987-02-03 Mitsubishi Heavy Ind Ltd Method of concentrating and purifying alcohol
JPS6225982A (en) * 1985-07-29 1987-02-03 Mitsubishi Heavy Ind Ltd Method of concentrating and purifying alcohol
US5053563A (en) * 1987-07-24 1991-10-01 Minister Of International Trade & Industry Method to concentrate and purify alcohol
FR2644453A1 (en) * 1989-03-20 1990-09-21 Centre Nat Rech Scient PROCESS FOR THE PREPARATION OF MONOFUNCTIONALIZED CYCLIC TETRAMINES
JPH0327336A (en) * 1989-06-26 1991-02-05 Tsuushiyousangiyoushiyou Kiso Sangiyoukiyokuchiyou Dehydration of alcohol

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014003475A1 (en) * 2012-06-28 2014-01-03 주식회사 엘지화학 Method for producing isopropyl alcohol
US8894823B2 (en) 2012-06-28 2014-11-25 Lg Chem, Ltd. Method for manufacturing isopropyl alcohol

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KR100219006B1 (en) 1999-09-01
MY112960A (en) 2001-10-31
DE69605460D1 (en) 2000-01-13
DE69605460T2 (en) 2000-07-20
TW338031B (en) 1998-08-11
SG50572A1 (en) 2003-07-18

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