AR035992A1 - Proceso para producir acido tereftalico puro con recuperacion mejorada de precursores, solvente y metil acetato - Google Patents
Proceso para producir acido tereftalico puro con recuperacion mejorada de precursores, solvente y metil acetatoInfo
- Publication number
- AR035992A1 AR035992A1 ARP000104953A ARP000104953A AR035992A1 AR 035992 A1 AR035992 A1 AR 035992A1 AR P000104953 A ARP000104953 A AR P000104953A AR P000104953 A ARP000104953 A AR P000104953A AR 035992 A1 AR035992 A1 AR 035992A1
- Authority
- AR
- Argentina
- Prior art keywords
- acid
- methyl acetate
- terephthalic acid
- recover
- acetic acid
- Prior art date
Links
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 title abstract 5
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 title abstract 5
- 239000002253 acid Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000002243 precursor Substances 0.000 title abstract 2
- 238000011084 recovery Methods 0.000 title 1
- 239000002904 solvent Substances 0.000 title 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 18
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract 14
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 abstract 6
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 abstract 6
- 239000008346 aqueous phase Substances 0.000 abstract 4
- 239000012074 organic phase Substances 0.000 abstract 4
- 239000012452 mother liquor Substances 0.000 abstract 3
- 239000007864 aqueous solution Substances 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 239000013078 crystal Substances 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000010924 continuous production Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 239000012071 phase Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/255—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
- C07C51/265—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Proceso continuo para producir ácido tereftálico puro de fórmula (1), mediante (a) primero hacer reaccionar el paraxileno con aire en presencia de ácido acético y un catalizador, a una presión y temperatura elevados para producir ácido tereftálico crudo; (b) recuperar el ácido tereftálico crudo, y una cantidad de ácido acético residual y ácido paratoluico, en forma de una torta húmeda; y (c) purificar el ácido tereftálico crudo al mezclarlo con agua y elevar la temperatura y presión de la mezcla para formar una solución acuosa, poner en contacto la solución acuosa con hidrógeno en presencia de un catalizador, ajustar la presión y temperatura de la solución hidrogenada mientras que se precipitan los cristales puros de ácido tereftálico, y el ácido acético residual y el ácido paratoluico residual permanecen en la solución hidrgenada para formar un licor madre purificado en planta, y recuperar los cristales puros de ácido tereftálico a partir del licor madre purificado en planta que comprende: (i) poner en contacto este licor madre purificado en planta con el paraxileno para formar un sistema de dos fases que comprende: una fase acuosa que contiene un ácido residual, y una fase orgánica que contiene ácido paratoluico y paraxileno; (ii) regresar la fase orgánica a la reacción de oxidación de la etapa (a); (iii) alimentar la fase acuosa a por lo menos un dispositivo de contacto adicional de manera simultánea con una corriente condensada que contiene agua, metil acetato y componentes orgánicos para formar una segunda fase acuosa y una segunda fase orgánica, mediante la cual el metil acetato y el ácido acético residual se particionan; y (iv) recuperar el metil acetato a partir de la segunda fase acuosa y recuperar el ácido acético a partir de la segunda fase orgánica. Este método permite recuperar y/o reciclar los precursores del ácido tereftálico, ácido acético residual y otros subproductos de las reacciones tal como el metil acetato.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/400,035 US6143926A (en) | 1999-09-21 | 1999-09-21 | Process for producing pure terephthalic acid with improved recovery of precursors, solvent and methyl acetate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR035992A1 true AR035992A1 (es) | 2004-08-04 |
Family
ID=23581959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000104953A AR035992A1 (es) | 1999-09-21 | 2000-09-21 | Proceso para producir acido tereftalico puro con recuperacion mejorada de precursores, solvente y metil acetato |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6143926A (es) |
| EP (1) | EP1214285B1 (es) |
| JP (1) | JP2003509484A (es) |
| KR (1) | KR100658555B1 (es) |
| CN (1) | CN1374937A (es) |
| AR (1) | AR035992A1 (es) |
| AT (1) | ATE254591T1 (es) |
| BR (1) | BR0014479A (es) |
| CA (1) | CA2380625C (es) |
| DE (1) | DE60006694T2 (es) |
| DZ (1) | DZ3061A1 (es) |
| EG (1) | EG22730A (es) |
| ES (1) | ES2209953T3 (es) |
| MX (1) | MXPA02003036A (es) |
| MY (1) | MY128616A (es) |
| TR (1) | TR200200715T2 (es) |
| TW (1) | TW506965B (es) |
| WO (1) | WO2001021571A1 (es) |
| ZA (1) | ZA200200892B (es) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100402482C (zh) * | 2003-02-21 | 2008-07-16 | 三菱化学株式会社 | 芳香羧酸的制备方法 |
| US7049465B2 (en) * | 2003-07-10 | 2006-05-23 | Eastman Chemical Company | Process for energy recovery in processes for the preparation of aromatic carboxylic acids |
| KR100650536B1 (ko) * | 2003-12-19 | 2006-11-27 | 미쓰이 가가쿠 가부시키가이샤 | 테레프탈산의 제조 방법 |
| US7213540B2 (en) * | 2004-02-05 | 2007-05-08 | Eastman Chemical Company | Steam recompression in carboxylic acid processes |
| US7504535B2 (en) | 2004-09-02 | 2009-03-17 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7495125B2 (en) | 2004-09-02 | 2009-02-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7608733B2 (en) | 2004-09-02 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7608732B2 (en) | 2005-03-08 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7586000B2 (en) | 2004-09-02 | 2009-09-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7572932B2 (en) | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7371894B2 (en) | 2004-09-02 | 2008-05-13 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7572936B2 (en) | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7741515B2 (en) | 2004-09-02 | 2010-06-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7361784B2 (en) | 2004-09-02 | 2008-04-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7399882B2 (en) | 2004-09-02 | 2008-07-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7582793B2 (en) | 2004-09-02 | 2009-09-01 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7589231B2 (en) | 2004-09-02 | 2009-09-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7910769B2 (en) | 2004-09-02 | 2011-03-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7692036B2 (en) | 2004-11-29 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7390921B2 (en) | 2004-09-02 | 2008-06-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7692037B2 (en) | 2004-09-02 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7381836B2 (en) | 2004-09-02 | 2008-06-03 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7568361B2 (en) | 2004-09-02 | 2009-08-04 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7507857B2 (en) | 2004-09-02 | 2009-03-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| CN1300088C (zh) * | 2005-03-25 | 2007-02-14 | 扬子石油化工股份有限公司 | 一种回收芳香族羧酸生产过程中原料、溶剂和副产物的方法 |
| US7884232B2 (en) | 2005-06-16 | 2011-02-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| KR100733400B1 (ko) * | 2005-08-01 | 2007-06-29 | 아신기술 주식회사 | 아세트산, 메틸아세테이트 및 물을 분리하기 위한공비증류공정 |
| US7358389B2 (en) | 2006-01-04 | 2008-04-15 | Eastman Chemical Company | Oxidation system employing internal structure for enhanced hydrodynamics |
| US7355068B2 (en) | 2006-01-04 | 2008-04-08 | Eastman Chemical Company | Oxidation system with internal secondary reactor |
| US8173835B2 (en) * | 2006-03-01 | 2012-05-08 | Grupo Petrotemex, S.A. De C.V. | Method and apparatus for drying carboxylic acid |
| US8697906B2 (en) * | 2006-03-01 | 2014-04-15 | Grupo Petrotemex, S.A. De C.V. | Methods and apparatus for producing a low-moisture carboxylic acid wet cake |
| KR100860343B1 (ko) * | 2007-03-15 | 2008-09-26 | 삼성석유화학(주) | 친환경적이고 단순화된 방향족 디카르복실산의 제조방법 |
| US9040746B2 (en) * | 2008-03-18 | 2015-05-26 | Gtc Technology Us, Llc | Systems and processes for the production of isophthalic acid and terephthalic acid |
| US8382961B2 (en) * | 2010-06-07 | 2013-02-26 | Amt International, Inc. | System and method for reduction of water consumption in purified terephthalic acid production |
| US20140121406A1 (en) * | 2012-10-31 | 2014-05-01 | Invista North America S.A.R.L. | Pure plant mother liquor solvent extraction system and method |
| JP2015140342A (ja) * | 2014-01-30 | 2015-08-03 | 株式会社日立製作所 | 精製テレフタル酸の製造方法 |
| TW201602078A (zh) * | 2014-04-08 | 2016-01-16 | 英威達技術有限公司 | 在經純化對苯二甲酸(pta)純化廠中最小化對-甲苯甲酸之回收 |
| CN114181065B (zh) * | 2021-12-24 | 2022-12-20 | 福州大学 | 一种节能降耗型的精对苯二甲酸生产方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2833816A (en) * | 1954-05-03 | 1958-05-06 | Mid Century Corp | Preparation of aromatic polycarboxylic acids |
| US4172209A (en) * | 1978-08-23 | 1979-10-23 | Uop Inc. | Process for producing dicarboxylic acids by the oxidation of xylene |
| US4500732A (en) * | 1983-09-15 | 1985-02-19 | Standard Oil Company (Indiana) | Process for removal and recycle of p-toluic acid from terephthalic acid crystallizer solvent |
| JP3729284B2 (ja) * | 1995-09-22 | 2005-12-21 | 三菱瓦斯化学株式会社 | 高純度テレフタル酸の製造方法 |
| TW483886B (en) * | 1998-08-11 | 2002-04-21 | Du Pont | Method for recovering methyl acetate and residual acetic acid in the production of pure terephtalic acid |
-
1999
- 1999-09-21 US US09/400,035 patent/US6143926A/en not_active Expired - Fee Related
-
2000
- 2000-07-03 MY MYPI20003031A patent/MY128616A/en unknown
- 2000-07-24 EG EG20000939A patent/EG22730A/xx active
- 2000-07-31 TW TW089115301A patent/TW506965B/zh not_active IP Right Cessation
- 2000-08-24 JP JP2001524952A patent/JP2003509484A/ja not_active Withdrawn
- 2000-08-24 BR BR0014479-7A patent/BR0014479A/pt not_active Application Discontinuation
- 2000-08-24 MX MXPA02003036A patent/MXPA02003036A/es active IP Right Grant
- 2000-08-24 KR KR1020027003708A patent/KR100658555B1/ko not_active Expired - Fee Related
- 2000-08-24 DE DE60006694T patent/DE60006694T2/de not_active Expired - Lifetime
- 2000-08-24 CA CA002380625A patent/CA2380625C/en not_active Expired - Fee Related
- 2000-08-24 ES ES00955870T patent/ES2209953T3/es not_active Expired - Lifetime
- 2000-08-24 CN CN00813072A patent/CN1374937A/zh active Pending
- 2000-08-24 TR TR2002/00715T patent/TR200200715T2/xx unknown
- 2000-08-24 EP EP00955870A patent/EP1214285B1/en not_active Expired - Lifetime
- 2000-08-24 AT AT00955870T patent/ATE254591T1/de not_active IP Right Cessation
- 2000-08-24 WO PCT/US2000/023224 patent/WO2001021571A1/en not_active Ceased
- 2000-09-20 DZ DZ000139A patent/DZ3061A1/xx active
- 2000-09-21 AR ARP000104953A patent/AR035992A1/es unknown
-
2002
- 2002-01-31 ZA ZA200200892A patent/ZA200200892B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY128616A (en) | 2007-02-28 |
| CN1374937A (zh) | 2002-10-16 |
| TR200200715T2 (tr) | 2002-09-23 |
| CA2380625C (en) | 2008-07-29 |
| ES2209953T3 (es) | 2004-07-01 |
| DE60006694D1 (de) | 2003-12-24 |
| DZ3061A1 (fr) | 2004-05-26 |
| DE60006694T2 (de) | 2004-12-09 |
| JP2003509484A (ja) | 2003-03-11 |
| BR0014479A (pt) | 2002-06-18 |
| KR20020029137A (ko) | 2002-04-17 |
| KR100658555B1 (ko) | 2006-12-18 |
| ATE254591T1 (de) | 2003-12-15 |
| WO2001021571A1 (en) | 2001-03-29 |
| CA2380625A1 (en) | 2001-03-29 |
| ZA200200892B (en) | 2003-03-26 |
| EP1214285A1 (en) | 2002-06-19 |
| TW506965B (en) | 2002-10-21 |
| EG22730A (en) | 2003-07-30 |
| MXPA02003036A (es) | 2002-10-23 |
| EP1214285B1 (en) | 2003-11-19 |
| US6143926A (en) | 2000-11-07 |
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| FB | Suspension of granting procedure |