SU1251796A3 - Способ выделени катализатора на основе ацетатов кобальта и марганца из остатка производства диметилтерефталата - Google Patents
Способ выделени катализатора на основе ацетатов кобальта и марганца из остатка производства диметилтерефталата Download PDFInfo
- Publication number
- SU1251796A3 SU1251796A3 SU853885102A SU3885102A SU1251796A3 SU 1251796 A3 SU1251796 A3 SU 1251796A3 SU 853885102 A SU853885102 A SU 853885102A SU 3885102 A SU3885102 A SU 3885102A SU 1251796 A3 SU1251796 A3 SU 1251796A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- residue
- reaction water
- cobalt
- catalyst
- manganese
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 title claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 229910017052 cobalt Inorganic materials 0.000 title claims description 13
- 239000010941 cobalt Substances 0.000 title claims description 13
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 title claims description 13
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 title claims description 5
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 title 2
- 229940011182 cobalt acetate Drugs 0.000 title 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 title 1
- 229960001826 dimethylphthalate Drugs 0.000 title 1
- 229940071125 manganese acetate Drugs 0.000 title 1
- 238000000926 separation method Methods 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 238000006243 chemical reaction Methods 0.000 claims abstract description 13
- 239000012074 organic phase Substances 0.000 claims abstract description 11
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 235000011054 acetic acid Nutrition 0.000 claims abstract description 5
- 235000019253 formic acid Nutrition 0.000 claims abstract description 5
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 5
- 239000011572 manganese Substances 0.000 claims abstract description 5
- 150000001243 acetic acids Chemical class 0.000 claims abstract description 3
- 150000004674 formic acids Chemical class 0.000 claims abstract description 3
- 238000000605 extraction Methods 0.000 claims abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 239000008346 aqueous phase Substances 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 5
- 238000007254 oxidation reaction Methods 0.000 claims description 5
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 230000032050 esterification Effects 0.000 claims description 3
- 238000005886 esterification reaction Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical compound CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- QSSJZLPUHJDYKF-UHFFFAOYSA-N methyl 4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C=C1 QSSJZLPUHJDYKF-UHFFFAOYSA-N 0.000 claims description 2
- 238000010992 reflux Methods 0.000 claims 2
- 150000001242 acetic acid derivatives Chemical class 0.000 claims 1
- 238000004508 fractional distillation Methods 0.000 claims 1
- 239000012071 phase Substances 0.000 abstract description 8
- 230000003197 catalytic effect Effects 0.000 abstract 1
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical class [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 abstract 1
- 230000029142 excretion Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/90—Regeneration or reactivation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/58—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Extraction Or Liquid Replacement (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3045332A DE3045332C2 (de) | 1980-12-02 | 1980-12-02 | Verfahren zur Gewinnung und Wiederverwendung von Schwermetalloxidationskatalysator aus Rückständen im Witten-DMT-Prozeß |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1251796A3 true SU1251796A3 (ru) | 1986-08-15 |
Family
ID=6118066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU853885102A SU1251796A3 (ru) | 1980-12-02 | 1985-04-26 | Способ выделени катализатора на основе ацетатов кобальта и марганца из остатка производства диметилтерефталата |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4464477A (enExample) |
| EP (1) | EP0053241B1 (enExample) |
| JP (1) | JPS609865B2 (enExample) |
| BR (1) | BR8107823A (enExample) |
| DE (2) | DE3045332C2 (enExample) |
| IN (1) | IN155427B (enExample) |
| SU (1) | SU1251796A3 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4868324A (en) * | 1988-05-24 | 1989-09-19 | Celanese Engineering Resins, Inc. | Purification of diphenyl phthalates |
| DE4026732A1 (de) * | 1990-08-24 | 1992-02-27 | Huels Chemische Werke Ag | Verfahren zur reinigung eines oxidationsabgases mit energierueckgewinnung |
| US5414106A (en) * | 1994-02-14 | 1995-05-09 | Hoechst Celanese Corporation | Process for recovering dimethyl terephthalate |
| DE19530970A1 (de) * | 1995-08-23 | 1997-02-27 | Huels Chemische Werke Ag | Verfahren zur Aufarbeitung von Rückständen aus der Rohester-Destillation bei der Herstellung von Dimethylterephthalat (DMT) |
| DE19618152C1 (de) * | 1996-05-07 | 1997-08-14 | Huels Chemische Werke Ag | Verfahren zur Trennung von Rohester im DMT-Prozeß |
| KR100450528B1 (ko) * | 1996-12-19 | 2004-11-26 | 에스케이케미칼주식회사 | 디메틸테레프탈레이트제조공정의슬러지로부터산화용촉매물질을회수하는방법 |
| KR19990025109A (ko) * | 1997-09-10 | 1999-04-06 | 조민호 | 테레프탈산 폐기슬러지로부터 코발트 촉매를 회수하는 방법 |
| US8575061B2 (en) | 2010-11-11 | 2013-11-05 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| US8575062B2 (en) | 2010-11-11 | 2013-11-05 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| US8658558B2 (en) | 2010-11-11 | 2014-02-25 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| US9168519B2 (en) | 2010-11-11 | 2015-10-27 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| SG190223A1 (en) | 2010-11-11 | 2013-06-28 | Chevron Usa Inc | Hydroconversion multi-metallic catalyst and method for making thereof |
| US8586500B2 (en) | 2010-11-11 | 2013-11-19 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| WO2014039735A2 (en) | 2012-09-05 | 2014-03-13 | Chevron U.S.A. Inc. | Hydroconversion multi-metallic catalyst and method for making thereof |
| CN105017022A (zh) * | 2015-07-20 | 2015-11-04 | 浙江大学 | 一种甲酯化回收利用pta氧化残渣的方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL70344B1 (enExample) * | 1971-10-28 | 1974-02-28 | ||
| DD104973A5 (enExample) * | 1972-09-12 | 1974-04-05 | ||
| JPS522896B2 (enExample) * | 1973-01-18 | 1977-01-25 | ||
| DE2427875C3 (de) * | 1974-06-10 | 1980-03-20 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur Gewinnung von Dimethylterephthalat und von Zwischenprodukten der Dimethylterephthalat-Herstellung |
| US4096340A (en) * | 1975-06-03 | 1978-06-20 | Teijin Hercules Chemical Co., Ltd. | Process for the preparation of dimethyl terephthalate |
| DE2923681C2 (de) * | 1979-06-12 | 1981-11-05 | Dynamit Nobel Ag, 5210 Troisdorf | Verfahren zur Gewinnung und Wiederverwendung von Schwermetalloxidationskatalysator aus dem Wittem-DMT-Prozeß |
| US4353810A (en) * | 1981-01-21 | 1982-10-12 | Hercofina | Minimizing iron in recovered oxidation catalyst material in DMT process |
-
1980
- 1980-12-02 DE DE3045332A patent/DE3045332C2/de not_active Expired
-
1981
- 1981-10-07 DE DE8181108022T patent/DE3166060D1/de not_active Expired
- 1981-10-07 EP EP81108022A patent/EP0053241B1/de not_active Expired
- 1981-11-26 IN IN1338/CAL/81A patent/IN155427B/en unknown
- 1981-12-01 US US06/326,175 patent/US4464477A/en not_active Expired - Lifetime
- 1981-12-01 BR BR8107823A patent/BR8107823A/pt unknown
- 1981-12-01 JP JP56191902A patent/JPS609865B2/ja not_active Expired
-
1985
- 1985-04-26 SU SU853885102A patent/SU1251796A3/ru active
Non-Patent Citations (1)
| Title |
|---|
| За вка DE № 2525135, . кл. С 07 С 69/82, опублик. 1976. Патент СССР № 1053735, кл. В 01 J 23/94, опублик. 1979. * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0053241B1 (de) | 1984-09-12 |
| BR8107823A (pt) | 1982-09-08 |
| DE3166060D1 (en) | 1984-10-18 |
| EP0053241A1 (de) | 1982-06-09 |
| DE3045332C2 (de) | 1982-11-25 |
| US4464477A (en) | 1984-08-07 |
| DE3045332A1 (de) | 1982-06-03 |
| IN155427B (enExample) | 1985-01-26 |
| JPS57119841A (en) | 1982-07-26 |
| JPS609865B2 (ja) | 1985-03-13 |
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