JPS6344734B2 - - Google Patents
Info
- Publication number
- JPS6344734B2 JPS6344734B2 JP57007492A JP749282A JPS6344734B2 JP S6344734 B2 JPS6344734 B2 JP S6344734B2 JP 57007492 A JP57007492 A JP 57007492A JP 749282 A JP749282 A JP 749282A JP S6344734 B2 JPS6344734 B2 JP S6344734B2
- Authority
- JP
- Japan
- Prior art keywords
- methacrylic acid
- gas
- aqueous
- scrubber
- tower
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 84
- 238000010521 absorption reaction Methods 0.000 claims description 34
- 238000000034 method Methods 0.000 claims description 26
- 238000001816 cooling Methods 0.000 claims description 21
- 239000007787 solid Substances 0.000 claims description 19
- 239000007788 liquid Substances 0.000 claims description 17
- 238000007254 oxidation reaction Methods 0.000 claims description 17
- 239000007795 chemical reaction product Substances 0.000 claims description 15
- 230000003647 oxidation Effects 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 230000003197 catalytic effect Effects 0.000 claims description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 6
- 239000012736 aqueous medium Substances 0.000 claims description 6
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 5
- 239000003507 refrigerant Substances 0.000 claims description 3
- 239000007789 gas Substances 0.000 description 63
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 20
- 239000003517 fume Substances 0.000 description 16
- 238000010791 quenching Methods 0.000 description 13
- 239000000243 solution Substances 0.000 description 12
- 230000000171 quenching effect Effects 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 9
- 239000002912 waste gas Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 238000009835 boiling Methods 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000004064 recycling Methods 0.000 description 3
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- -1 aromatic carboxylic acids Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011964 heteropoly acid Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- AMWVZPDSWLOFKA-UHFFFAOYSA-N phosphanylidynemolybdenum Chemical compound [Mo]#P AMWVZPDSWLOFKA-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000011165 process development Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 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
-
- 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
- C07C51/47—Separation; Purification; Stabilisation; Use of additives by solid-liquid treatment; by chemisorption
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
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Claims (1)
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57007492A JPS58126831A (ja) | 1982-01-22 | 1982-01-22 | ã¡ã¿ã¯ãªã«é žã®æéæ¹æ³ |
DE3301983A DE3301983C2 (de) | 1982-01-22 | 1983-01-21 | Verfahren zur Isolierung von MethacrylsÀure |
GB08301621A GB2116963B (en) | 1982-01-22 | 1983-01-21 | Method of isolating methacrylic acid |
FR8300989A FR2520357A1 (fr) | 1982-01-22 | 1983-01-24 | Procede pour isoler l'acide methacrylique d'un produit de reaction gazeux resultant de l'oxydation catalytique, par exemple de l'isobutylene, en phase vapeur |
US07/003,864 US4925981A (en) | 1982-01-22 | 1987-01-16 | Method of isolating methacrylic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57007492A JPS58126831A (ja) | 1982-01-22 | 1982-01-22 | ã¡ã¿ã¯ãªã«é žã®æéæ¹æ³ |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58126831A JPS58126831A (ja) | 1983-07-28 |
JPS6344734B2 true JPS6344734B2 (ja) | 1988-09-06 |
Family
ID=11667266
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57007492A Granted JPS58126831A (ja) | 1982-01-22 | 1982-01-22 | ã¡ã¿ã¯ãªã«é žã®æéæ¹æ³ |
Country Status (5)
Country | Link |
---|---|
US (1) | US4925981A (ja) |
JP (1) | JPS58126831A (ja) |
DE (1) | DE3301983C2 (ja) |
FR (1) | FR2520357A1 (ja) |
GB (1) | GB2116963B (ja) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3721865A1 (de) * | 1987-07-02 | 1989-01-12 | Basf Ag | Verfahren zur herstellung von methacrylsaeure |
DE4132684A1 (de) * | 1991-10-01 | 1993-04-08 | Basf Ag | Verfahren zur katalytischen gasphasenoxidation von methacrolein zu methacrylsaeure |
DE4436243A1 (de) * | 1994-10-11 | 1996-04-18 | Basf Ag | Verfahren zur Abtrennung von (Meth)acrylsÀure aus dem Reaktionsgasgemisch der katalytischen Gasphasenoxidation C¶3¶-/C¶4¶-Verbindungen |
DE19624674A1 (de) * | 1996-06-20 | 1998-01-02 | Basf Ag | Verfahren zur Entsorgung von bei der AcrylsÀure- oder MethacrylsÀure-Herstellung anfallenden Nebenkomponenten |
US5877345A (en) * | 1997-02-07 | 1999-03-02 | Rohm And Haas Company | Process for producing butyl acrylate |
DE19752199A1 (de) * | 1997-11-25 | 1999-05-27 | Basf Ag | Verfahren zur Kondensation |
DE19754155A1 (de) * | 1997-12-05 | 1999-06-10 | Basf Ag | Verfahren zum KÃŒhlen von heiÃen Gasen |
DE60005870T2 (de) * | 1999-03-05 | 2004-08-19 | Rohm And Haas Co. | Verfahren zur Herstellung von AcrylsÀure |
JP4553440B2 (ja) * | 2000-03-10 | 2010-09-29 | äžè±ã¬ã€ãšã³æ ªåŒäŒç€Ÿ | ã¡ã¿ã¯ãªã«é žã®è£œé æ¹æ³ |
JP4673958B2 (ja) * | 2000-06-19 | 2011-04-20 | æ ªåŒäŒç€Ÿæ¥æ¬è§Šåª | åºåœ¢ç©é€å»è£ 眮 |
JP2003238485A (ja) * | 2001-12-10 | 2003-08-27 | Nippon Shokubai Co Ltd | ïŒã¡ã¿ïŒã¢ã¯ãªã«é žã®æéæ¹æ³ããã³è£ 眮 |
US20040143149A1 (en) * | 2002-08-02 | 2004-07-22 | Decourcy Michael Stanley | Method for reducing nitrogen oxide emissions in industrial process |
US7649112B2 (en) * | 2005-07-25 | 2010-01-19 | Saudi Basic Industries Corporation | Integrated plant for producing 2-ethyl-hexanol and methacrylic acid and a method based thereon |
US7799946B2 (en) * | 2007-02-14 | 2010-09-21 | Saudi Basic Industries Corporation | Process for separating methacrolein from methacrylic acid in a gas phase product from the partial oxidation of isobutene |
BR112013022304B1 (pt) | 2011-03-11 | 2020-01-28 | Lg Chemical Ltd | método de recuperação contÃnua de ácido (met)acrÃlico |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3388897A (en) * | 1958-11-28 | 1968-06-18 | Automotive Rubber Co Inc | Apparatus for separating and collecting particles carried by gases |
US3405172A (en) * | 1962-12-19 | 1968-10-08 | Distillers Co Yeast Ltd | Preparation of acrylic acid with the prevention of formation of acrylic polymers |
US3433840A (en) * | 1966-12-29 | 1969-03-18 | Sumitomo Chemical Co | Process for recovering acrolein by quenching,absorption and plural distillation |
US3664968A (en) * | 1967-11-16 | 1972-05-23 | Goodrich Co B F | Catalyst for preparing unsaturated acids and aldehydes |
JPS6059891B2 (ja) * | 1977-09-28 | 1985-12-27 | äœåååŠå·¥æ¥æ ªåŒäŒç€Ÿ | ã¡ã¿ã¯ãã¬ã€ã³ããã³ã¡ã¿ã¯ãªã«é žã®åé¢æ¹æ³ |
JPS6016927B2 (ja) * | 1979-07-19 | 1985-04-30 | äžè±ã¬ã€ãšã³æ ªåŒäŒç€Ÿ | ã¡ã¿ã¯ãªã«é žã®æœåºåé¢æ³ |
JPS56113732A (en) * | 1980-02-12 | 1981-09-07 | Nippon Kayaku Co Ltd | Preparation of methacrylic acid |
JPS5791944A (en) * | 1980-12-01 | 1982-06-08 | Nippon Kayaku Co Ltd | Recovery of methacrolein and/or methacrylic acid, and quenching tower |
-
1982
- 1982-01-22 JP JP57007492A patent/JPS58126831A/ja active Granted
-
1983
- 1983-01-21 GB GB08301621A patent/GB2116963B/en not_active Expired
- 1983-01-21 DE DE3301983A patent/DE3301983C2/de not_active Expired
- 1983-01-24 FR FR8300989A patent/FR2520357A1/fr active Granted
-
1987
- 1987-01-16 US US07/003,864 patent/US4925981A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE3301983A1 (de) | 1983-08-18 |
FR2520357B1 (ja) | 1985-03-29 |
FR2520357A1 (fr) | 1983-07-29 |
US4925981A (en) | 1990-05-15 |
GB2116963A (en) | 1983-10-05 |
GB8301621D0 (en) | 1983-02-23 |
DE3301983C2 (de) | 1985-07-04 |
GB2116963B (en) | 1985-11-27 |
JPS58126831A (ja) | 1983-07-28 |
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