TWI302147B - Method of producing unsaturated aldehyde and unsaturated acid in fixed-bed catalytic partial oxidation reactor with enhanced heat control system - Google Patents
Method of producing unsaturated aldehyde and unsaturated acid in fixed-bed catalytic partial oxidation reactor with enhanced heat control system Download PDFInfo
- Publication number
- TWI302147B TWI302147B TW093126176A TW93126176A TWI302147B TW I302147 B TWI302147 B TW I302147B TW 093126176 A TW093126176 A TW 093126176A TW 93126176 A TW93126176 A TW 93126176A TW I302147 B TWI302147 B TW I302147B
- Authority
- TW
- Taiwan
- Prior art keywords
- temperature
- reaction zone
- catalyst
- unsaturated
- layer
- Prior art date
Links
- 230000003197 catalytic effect Effects 0.000 title claims description 56
- 238000000034 method Methods 0.000 title claims description 45
- 239000002253 acid Substances 0.000 title claims description 27
- 238000007254 oxidation reaction Methods 0.000 title claims description 23
- 230000003647 oxidation Effects 0.000 title claims description 13
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title 1
- 238000006243 chemical reaction Methods 0.000 claims description 185
- 239000003054 catalyst Substances 0.000 claims description 116
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims description 62
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 52
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 49
- 238000012546 transfer Methods 0.000 claims description 38
- 238000005192 partition Methods 0.000 claims description 29
- 230000008569 process Effects 0.000 claims description 28
- 239000000463 material Substances 0.000 claims description 25
- 230000000694 effects Effects 0.000 claims description 23
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 21
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 21
- 230000001629 suppression Effects 0.000 claims description 19
- 150000001299 aldehydes Chemical class 0.000 claims description 16
- 230000001965 increasing effect Effects 0.000 claims description 16
- 239000000376 reactant Substances 0.000 claims description 13
- 150000001336 alkenes Chemical class 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 238000000926 separation method Methods 0.000 claims description 10
- 150000007513 acids Chemical class 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 230000002401 inhibitory effect Effects 0.000 claims description 7
- 239000007858 starting material Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims 4
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 238000009738 saturating Methods 0.000 claims 1
- 238000000638 solvent extraction Methods 0.000 claims 1
- 239000010410 layer Substances 0.000 description 117
- 150000003839 salts Chemical class 0.000 description 46
- 230000000052 comparative effect Effects 0.000 description 24
- 230000001276 controlling effect Effects 0.000 description 11
- 238000011049 filling Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 238000009825 accumulation Methods 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 125000006850 spacer group Chemical group 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 5
- 238000010276 construction Methods 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- -1 U.S. Patent No. 3 Chemical class 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 230000020169 heat generation Effects 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 229910052707 ruthenium Inorganic materials 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000003723 Smelting Methods 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 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
- 238000001816 cooling Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 241000233805 Phoenix Species 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical class [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- XDXFALYQLCMAQN-BTJKTKAUSA-N butanedioic acid;(z)-but-2-enedioic acid Chemical compound OC(=O)CCC(O)=O.OC(=O)\C=C/C(O)=O XDXFALYQLCMAQN-BTJKTKAUSA-N 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910000420 cerium oxide Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- OUFGXIPMNQFUES-UHFFFAOYSA-N molybdenum ruthenium Chemical compound [Mo].[Ru] OUFGXIPMNQFUES-UHFFFAOYSA-N 0.000 description 1
- WUJISAYEUPRJOG-UHFFFAOYSA-N molybdenum vanadium Chemical compound [V].[Mo] WUJISAYEUPRJOG-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
-
- 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
- C07C51/25—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
- C07C51/252—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring of propene, butenes, acrolein or methacrolein
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20030060736 | 2003-09-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200523244A TW200523244A (en) | 2005-07-16 |
| TWI302147B true TWI302147B (en) | 2008-10-21 |
Family
ID=36204412
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW093126176A TWI302147B (en) | 2003-09-01 | 2004-08-31 | Method of producing unsaturated aldehyde and unsaturated acid in fixed-bed catalytic partial oxidation reactor with enhanced heat control system |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7238836B2 (enExample) |
| EP (1) | EP1660226A4 (enExample) |
| JP (1) | JP4762899B2 (enExample) |
| KR (1) | KR100553825B1 (enExample) |
| CN (1) | CN1845785B (enExample) |
| IN (2) | IN227312B (enExample) |
| TW (1) | TWI302147B (enExample) |
| WO (1) | WO2005021149A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101429109B (zh) * | 2003-12-24 | 2012-10-03 | Lg化学株式会社 | 在具有提高热控制系统的固定床催化部分氧化反应器中制备不饱和酸的方法 |
| KR100677051B1 (ko) * | 2005-03-18 | 2007-02-01 | 주식회사 엘지화학 | 올레핀으로부터 불포화산을 제조하는 방법 |
| KR100868454B1 (ko) * | 2005-07-08 | 2008-11-11 | 주식회사 엘지화학 | 고정층 촉매 부분산화 반응기에서 고효율의 불포화산의제조방법 |
| KR100807972B1 (ko) * | 2005-08-10 | 2008-02-28 | 주식회사 엘지화학 | 아크릴산 선택성이 높은 복합 금속 산화물 촉매 |
| EP1734030A1 (de) * | 2006-01-18 | 2006-12-20 | BASF Aktiengesellschaft | Verfahren zum Langzeitbetrieb einer heterogen katalysierten partiellen Gasphasenoxidation einer organischen Ausgangsverbindung |
| KR100873271B1 (ko) * | 2006-03-13 | 2008-12-11 | 주식회사 엘지화학 | 고정층 촉매 부분산화 반응기에서 고효율의 불포화알데히드 및/또는 불포화 지방산의 제조방법 |
| EP2059334A1 (de) * | 2006-11-15 | 2009-05-20 | Basf Se | Verfahren zum betreiben einer exothermen heterogen katalysierten partiellen gasphasenoxidation einer organischen ausgangsverbindung zu einer organischen zielverbindung |
| WO2008120956A1 (en) * | 2007-04-03 | 2008-10-09 | Lg Chem, Ltd. | Method for preparing unsaturated aldehyde and/or unsaturated fatty acid using fixed-bed catalytic partial oxidation reactor |
| JP5559692B2 (ja) * | 2008-09-22 | 2014-07-23 | 株式会社日本触媒 | 固定床反応器、およびそれを用いたアクリル酸の製造方法 |
| AU2011201715B8 (en) * | 2010-04-15 | 2014-08-21 | China Petroleum & Chemical Corporation | A process for selective oxidative dehydrogenation of a hydrogen-containing co mixed gas |
| DE102010048405A1 (de) * | 2010-10-15 | 2011-05-19 | Basf Se | Verfahren zum Langzeitbetrieb einer heterogen katalysierten partiellen Gasphasenoxidation von Proben zu Acrolein |
| CN103347845B (zh) * | 2011-02-02 | 2015-04-01 | 日本化药株式会社 | 制造不饱和醛和/或不饱和羧酸的方法 |
| CN108752198A (zh) * | 2014-04-30 | 2018-11-06 | 三菱化学株式会社 | （甲基）丙烯酸的制造方法 |
| GB201506572D0 (en) * | 2015-04-17 | 2015-06-03 | Johnson Matthey Davy Technologies Ltd | Process |
| JP6752035B2 (ja) * | 2016-03-29 | 2020-09-09 | 日本化薬株式会社 | 再スタートアップ方法 |
| KR102084768B1 (ko) | 2016-11-01 | 2020-03-04 | 주식회사 엘지화학 | 불포화 알데하이드 및 불포화 카르복실산의 제조 방법 |
| JP7599367B2 (ja) * | 2021-03-31 | 2024-12-13 | 三菱重工業株式会社 | 触媒反応装置、この触媒反応装置において流体状生成物を得るための方法、及び、この触媒反応装置の製造方法 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3147084A (en) * | 1962-03-08 | 1964-09-01 | Shell Oil Co | Tubular catalytic reactor with cooler |
| DE2056614C3 (de) * | 1970-11-18 | 1981-04-16 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Acrylsäure aus Propylen |
| BE793928A (fr) * | 1972-01-13 | 1973-05-02 | Deggendorfer Werft Eisenbau | Appareil pour la mise en oeuvre de processus chimiques exothermiques et endothermiques |
| US4028070A (en) * | 1974-04-11 | 1977-06-07 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Method of recovering ethylene oxide |
| AU529228B2 (en) * | 1977-07-13 | 1983-06-02 | Nippon Shokubai Kagaku Kogyo Co. Ltd. | Catalytic vapour phase oxidation |
| JPS6029290B2 (ja) | 1977-07-20 | 1985-07-10 | 株式会社日本触媒 | 接触気相酸化方法 |
| JPS55113730A (en) * | 1979-02-26 | 1980-09-02 | Mitsubishi Petrochem Co Ltd | Preparation of acrolein and acrylic acid |
| AU606160B2 (en) | 1987-05-27 | 1991-01-31 | Nippon Shokubai Kagaku Kogyo Co. Ltd. | Process for production of acrylic acid |
| JPH0784400B2 (ja) * | 1990-04-03 | 1995-09-13 | 株式会社日本触媒 | 不飽和アルデヒドおよび不飽和酸の製造方法 |
| DE4431949A1 (de) * | 1994-09-08 | 1995-03-16 | Basf Ag | Verfahren zur katalytischen Gasphasenoxidation von Acrolein zu Acrylsäure |
| DE4431957A1 (de) * | 1994-09-08 | 1995-03-16 | Basf Ag | Verfahren zur katalytischen Gasphasenoxidation von Propen zu Acrolein |
| JP3537253B2 (ja) * | 1996-03-06 | 2004-06-14 | 株式会社日本触媒 | アクリル酸の製造方法 |
| JP3804875B2 (ja) * | 1996-06-05 | 2006-08-02 | 旭化成ケミカルズ株式会社 | メタクロレインの製造方法 |
| JP3775872B2 (ja) * | 1996-12-03 | 2006-05-17 | 日本化薬株式会社 | アクロレイン及びアクリル酸の製造方法 |
| JP2863509B2 (ja) * | 1997-04-16 | 1999-03-03 | 株式会社日本触媒 | メタクロレインおよびメタクリル酸の製造方法 |
| JP3463529B2 (ja) * | 1997-09-04 | 2003-11-05 | 東亞合成株式会社 | 気相接触酸化反応方法及び反応器 |
| JP3948798B2 (ja) * | 1997-10-27 | 2007-07-25 | 株式会社日本触媒 | アクリル酸の製造方法 |
| TW524796B (en) * | 1997-11-17 | 2003-03-21 | Sumitomo Chemical Co | Method for producing acrylic acid |
| US6384274B1 (en) * | 1998-09-27 | 2002-05-07 | Rohm And Haas Company | Single reactor process for preparing acrylic acid from propylene having improved capacity |
| DE19910508A1 (de) * | 1999-03-10 | 2000-09-21 | Basf Ag | Verfahren der katalytischen Gasphasenoxidation von Acrolein zu Acrylsäure |
| MY121141A (en) * | 1999-03-10 | 2005-12-30 | Basf Ag | Method for the catalytic gas-phase oxidation of propene into acrolein |
| MY119958A (en) * | 1999-03-10 | 2005-08-30 | Basf Ag | Catalytic gas-phase oxidation of propene to acrylic acid |
| JP4308372B2 (ja) * | 1999-07-06 | 2009-08-05 | 株式会社日本触媒 | （メタ）アクリル酸および／または（メタ）アクロレインの吸収方法及びその装置 |
| DE60035746T2 (de) * | 1999-08-31 | 2008-04-30 | Nippon Shokubai Co., Ltd. | Reaktor zur katalytischen Gasphasenoxidation |
| JP3895527B2 (ja) * | 1999-08-31 | 2007-03-22 | 株式会社日本触媒 | 接触気相酸化方法 |
| JP3732080B2 (ja) * | 1999-08-31 | 2006-01-05 | 株式会社日本触媒 | 接触気相酸化反応器 |
| ZA200004211B (en) | 1999-08-31 | 2001-02-14 | Nippon Catalytic Chem Ind | Method for catalytic gas phase oxidation. |
| JP3646027B2 (ja) * | 1999-11-05 | 2005-05-11 | 株式会社日本触媒 | 接触気相酸化用反応器およびそれを使用した（メタ）アクリル酸の製造方法 |
| US6620968B1 (en) * | 1999-11-23 | 2003-09-16 | Rohm And Haas Company | High hydrocarbon space velocity process for preparing unsaturated aldehydes and acids |
| JP3943311B2 (ja) * | 2000-05-19 | 2007-07-11 | 株式会社日本触媒 | 不飽和アルデヒドおよび不飽和カルボン酸の製造方法 |
| JP4497442B2 (ja) * | 2001-01-16 | 2010-07-07 | 三菱レイヨン株式会社 | メタクロレインおよびメタクリル酸の製造方法 |
| KR100450234B1 (ko) | 2002-07-10 | 2004-09-24 | 주식회사 엘지화학 | 개선된 열교환 시스템을 갖는 촉매 산화 반응기 |
| CN101429109B (zh) * | 2003-12-24 | 2012-10-03 | Lg化学株式会社 | 在具有提高热控制系统的固定床催化部分氧化反应器中制备不饱和酸的方法 |
-
2004
- 2004-08-31 TW TW093126176A patent/TWI302147B/zh not_active IP Right Cessation
- 2004-08-31 KR KR1020040069117A patent/KR100553825B1/ko not_active Expired - Lifetime
- 2004-09-01 EP EP04774454A patent/EP1660226A4/en not_active Withdrawn
- 2004-09-01 WO PCT/KR2004/002193 patent/WO2005021149A1/en not_active Ceased
- 2004-09-01 US US10/931,034 patent/US7238836B2/en not_active Expired - Lifetime
- 2004-09-01 CN CN2004800250247A patent/CN1845785B/zh not_active Expired - Lifetime
- 2004-09-01 IN IN384KO2006 patent/IN227312B/en unknown
- 2004-09-01 JP JP2006523141A patent/JP4762899B2/ja not_active Expired - Fee Related
-
2006
- 2006-02-21 IN IN384KON2006 patent/IN2006KO00384A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR100553825B1 (ko) | 2006-02-21 |
| JP4762899B2 (ja) | 2011-08-31 |
| JP2007533605A (ja) | 2007-11-22 |
| CN1845785A (zh) | 2006-10-11 |
| EP1660226A1 (en) | 2006-05-31 |
| EP1660226A4 (en) | 2011-03-16 |
| US20050049435A1 (en) | 2005-03-03 |
| KR20050024206A (ko) | 2005-03-10 |
| IN227312B (enExample) | 2009-01-09 |
| WO2005021149A1 (en) | 2005-03-10 |
| US7238836B2 (en) | 2007-07-03 |
| IN2006KO00384A (enExample) | 2007-08-03 |
| CN1845785B (zh) | 2010-04-14 |
| TW200523244A (en) | 2005-07-16 |
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