JPH08245494A - プロパンからアクロレイン、アクリル酸又はこれらの混合物を製造する方法 - Google Patents
プロパンからアクロレイン、アクリル酸又はこれらの混合物を製造する方法Info
- Publication number
- JPH08245494A JPH08245494A JP8050643A JP5064396A JPH08245494A JP H08245494 A JPH08245494 A JP H08245494A JP 8050643 A JP8050643 A JP 8050643A JP 5064396 A JP5064396 A JP 5064396A JP H08245494 A JPH08245494 A JP H08245494A
- Authority
- JP
- Japan
- Prior art keywords
- propylene
- propane
- mixture
- oxidation
- acrylic acid
- 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.)
- Withdrawn
Links
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 134
- 239000000203 mixture Substances 0.000 title claims abstract description 103
- 239000001294 propane Substances 0.000 title claims abstract description 67
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 title claims abstract description 66
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 title claims abstract description 45
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 238000004519 manufacturing process Methods 0.000 title abstract description 14
- 239000007789 gas Substances 0.000 claims abstract description 148
- 230000003647 oxidation Effects 0.000 claims abstract description 91
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 91
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 89
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 88
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims abstract description 29
- 230000009471 action Effects 0.000 claims abstract description 26
- 229910001882 dioxygen Inorganic materials 0.000 claims abstract description 25
- 238000006356 dehydrogenation reaction Methods 0.000 claims abstract description 22
- 239000002638 heterogeneous catalyst Substances 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims description 50
- 229910052760 oxygen Inorganic materials 0.000 claims description 30
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 29
- 239000001301 oxygen Substances 0.000 claims description 29
- 230000008569 process Effects 0.000 claims description 26
- 239000003054 catalyst Substances 0.000 claims description 19
- 150000002894 organic compounds Chemical class 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 238000000926 separation method Methods 0.000 abstract description 9
- 230000001590 oxidative effect Effects 0.000 abstract description 8
- 239000012808 vapor phase Substances 0.000 abstract description 3
- 230000003134 recirculating effect Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 38
- 239000003701 inert diluent Substances 0.000 description 36
- 239000000047 product Substances 0.000 description 33
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 26
- 239000012071 phase Substances 0.000 description 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- 239000011261 inert gas Substances 0.000 description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 238000007210 heterogeneous catalysis Methods 0.000 description 12
- 238000004880 explosion Methods 0.000 description 11
- 229910002091 carbon monoxide Inorganic materials 0.000 description 10
- 239000006227 byproduct Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- 239000007800 oxidant agent Substances 0.000 description 7
- 239000001569 carbon dioxide Substances 0.000 description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- 229930195734 saturated hydrocarbon Natural products 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000007865 diluting Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000012495 reaction gas Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- -1 methane Natural products 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 241000282461 Canis lupus Species 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010405 reoxidation reaction Methods 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids
- C07C57/04—Acrylic acid; Methacrylic acid
-
- 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
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
- C07C45/34—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
- C07C45/35—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds in propene or isobutene
-
- 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
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/33—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties
-
- 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)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19508558A DE19508558A1 (de) | 1995-03-10 | 1995-03-10 | Verfahren zur Herstellung von Acrolein, Acrylsäure oder deren Gemisch aus Propan |
| DE19525504.6 | 1995-07-13 | ||
| DE19508558.2 | 1995-07-13 | ||
| DE1995125504 DE19525504A1 (de) | 1995-07-13 | 1995-07-13 | Verfahren zur Herstellung von Acrolein, Acrylsäure oder deren Gemisch aus Propan |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08245494A true JPH08245494A (ja) | 1996-09-24 |
Family
ID=26013226
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8050643A Withdrawn JPH08245494A (ja) | 1995-03-10 | 1996-03-07 | プロパンからアクロレイン、アクリル酸又はこれらの混合物を製造する方法 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5705684A (enExample) |
| EP (1) | EP0731077B1 (enExample) |
| JP (1) | JPH08245494A (enExample) |
| KR (1) | KR960034158A (enExample) |
| CN (1) | CN1086690C (enExample) |
| CA (1) | CA2171417A1 (enExample) |
| CZ (1) | CZ73396A3 (enExample) |
| DE (1) | DE59603316D1 (enExample) |
| ES (1) | ES2139266T3 (enExample) |
| SG (1) | SG40844A1 (enExample) |
| TW (1) | TW328534B (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004526800A (ja) * | 2001-05-07 | 2004-09-02 | ビーエーエスエフ アクチェンゲゼルシャフト | プロパンの不均一系触媒部分酸化によるアクリル酸の製法 |
| JP2006500430A (ja) * | 2002-09-27 | 2006-01-05 | ビーエーエスエフ アクチェンゲゼルシャフト | プロピレンの少なくとも１種の部分酸化‐及び／又はアンモ酸化生成物の製法 |
| WO2009008422A1 (ja) * | 2007-07-11 | 2009-01-15 | Sumitomo Chemical Company, Limited | 混合ガスの製造方法および製造装置、ならびにエポキシ化合物の製造装置および製造方法 |
| JP2009517358A (ja) * | 2005-11-24 | 2009-04-30 | ビーエーエスエフ ソシエタス・ヨーロピア | プロパンからのアクロレイン、又はアクリル酸、又はその混合物の製法 |
| JP2009520586A (ja) * | 2005-12-21 | 2009-05-28 | ビーエーエスエフ ソシエタス・ヨーロピア | 少なくとも１つの脱水素化される炭化水素の連続的不均一触媒部分脱水素化方法 |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6492548B1 (en) | 1996-04-01 | 2002-12-10 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the oxidation of alkanes |
| EP0891316B1 (en) * | 1996-04-01 | 2003-05-21 | Union Carbide Chemicals & Plastics Technology Corporation | Processes for the manufacture of methylmercaptopropanal |
| DE19740252A1 (de) | 1997-09-12 | 1999-03-18 | Basf Ag | Verfahren zur Herstellung von Acrylsäure und Methacrylsäure |
| SG81982A1 (en) * | 1998-05-18 | 2001-07-24 | Nippon Catalytic Chem Ind | Method for production of acrolein and acrylic acid |
| DE19833049A1 (de) | 1998-07-22 | 2000-01-27 | Basf Ag | Verfahren zur Herstellung von Acrylsäure |
| DE19838795A1 (de) | 1998-08-26 | 2000-03-02 | Basf Ag | Verfahren zur kontinuierlichen Gewinnung von (Meth)acrylsäure |
| DE10028582A1 (de) * | 2000-06-14 | 2001-12-20 | Basf Ag | Verfahren zur Herstellung von Acrolein oder Acrylsäure oder deren Gemischen aus Propan |
| ES2480302T3 (es) | 2000-06-14 | 2014-07-25 | Basf Se | Procedimiento para la preparación de acroleína o ácido acrílico o su mezcla a partir de propano |
| DE10031518A1 (de) * | 2000-06-28 | 2002-01-10 | Basf Ag | Verfahren zur Herstellung von Hydroformylierungsprodukten des Propylens und von Acrylsäure und/oder Acrolein |
| US6734136B2 (en) * | 2000-09-28 | 2004-05-11 | Rohm And Haas Company | IR and/or SM promoted multi-metal oxide catalyst |
| US6403525B1 (en) * | 2000-09-28 | 2002-06-11 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| KR100814702B1 (ko) * | 2000-09-28 | 2008-03-18 | 롬 앤드 하스 캄파니 | 불포화 니트릴 제조방법 |
| US6407031B1 (en) * | 2000-09-28 | 2002-06-18 | Rohm And Haas Company | Promoted multi-metal oxide catalyst |
| US7049466B2 (en) * | 2000-09-29 | 2006-05-23 | Rohm And Haas Company | Recycle process |
| FR2844262B1 (fr) * | 2002-09-10 | 2004-10-15 | Atofina | Procede de fabrication d'acide acrylique a partir de propane, en l'absence d'oxygene moleculaire |
| DE10316039A1 (de) | 2003-04-07 | 2004-10-21 | Basf Ag | Verfahren zur Herstellung von wenigstens einem partiellen Oxidations-und/oder Ammoxidationsprodukt eines Kohlenwasserstoffs |
| US7589046B2 (en) | 2003-06-04 | 2009-09-15 | Basf Aktiengesellschaft | Thermal treatment of the precursor material of a catalytically active material |
| JP2005144432A (ja) * | 2003-11-18 | 2005-06-09 | Rohm & Haas Co | アルカンをアルケン、およびそれらの対応する酸素化生成物に転化するための触媒系 |
| TWI303584B (en) * | 2004-04-08 | 2008-12-01 | Rohm & Haas | Improved catalytic (amm)oxidation process for conversion of lower alkanes |
| US8431743B2 (en) * | 2004-07-01 | 2013-04-30 | Basf Aktiengesellschaft | Preparation of acrylic acid by heterogeneously catalyzed partial gas phase oxidation of propylene |
| CN1980879B (zh) * | 2004-07-01 | 2011-03-02 | 巴斯福股份公司 | 由丙烷生产丙烯醛、丙烯酸或其混合物的方法 |
| WO2006002708A1 (de) * | 2004-07-01 | 2006-01-12 | Basf Aktiengesellschaft | Verfahren zur herstellung von acrolein oder acrylsäure oder deren gemisch durch heterogen katalysierte partielle gasphasenoxidation von propylen |
| WO2006002703A1 (de) * | 2004-07-01 | 2006-01-12 | Basf Aktiengesellschaft | Verfahren zur herstellung von acrylsäure durch heterogen katalysierte partielle gasphasen oxidation von propylen |
| US7361622B2 (en) * | 2005-11-08 | 2008-04-22 | Rohm And Haas Company | Multi-staged catalyst systems and process for converting alkanes to alkenes and to their corresponding oxygenated products |
| DE102005038412A1 (de) * | 2005-08-12 | 2007-02-15 | Basf Ag | Verfahren zur Deckung des Bedarfs an Polymerisaten I, die zu wenigstens 90% ihres Gewichtes Acrylsäure, deren Salze und/oder Alkylester der Acrylsäure radikalisch einpolymerisiert enthalten |
| US20070106088A1 (en) * | 2005-11-08 | 2007-05-10 | Abraham Benderly | Hybrid catalyst systems and hybrid process for converting alkanes to alkenes and to their corresponding oxygenated products |
| KR101370749B1 (ko) | 2005-11-24 | 2014-03-06 | 바스프 에스이 | 프로판으로부터 아크롤레인 또는 아크릴산, 또는 그의혼합물의 제조 방법 |
| DE102006024901A1 (de) | 2006-05-24 | 2007-11-29 | Basf Ag | Verfahren zur Herstellung von Acrolein, oder Acrylsäure oder deren Gemisch aus Propan |
| DE102006029790A1 (de) | 2006-06-27 | 2008-01-03 | Basf Ag | Verfahren der kontinuierlichen heterogen katalysierten partiellen Dehydrierung wenigstens eines zu dehydrierenden Kohlenwasserstoffs |
| DE102007006647A1 (de) | 2007-02-06 | 2008-08-07 | Basf Se | Verfahren zur Regenerierung eines im Rahmen einer heterogen katalysierten partiellen Dehydrierung eines Kohlenwasserstoffs deaktivierten Katalysatorbetts |
| BRPI0814212A2 (pt) * | 2007-07-11 | 2015-01-27 | Sumitomo Chemical Co | Aparelho e método para produzir composto de époxi. |
| MX2008015540A (es) | 2007-12-26 | 2009-06-26 | Rohm Ahd Haas Company | Un proceso integrado para preparar un acido carboxilico a partir de un alcano. |
| DE102008020688B3 (de) * | 2008-04-24 | 2009-11-05 | Evonik Stockhausen Gmbh | Verfahren zur Herstellung und Aufreinigung wässriger Phasen |
| EP2143701B1 (en) * | 2008-07-10 | 2011-03-02 | Rohm and Haas Company | Hybrid autothermal catalytic process for converting alkanes to alkenes and catalysts useful for same |
| EP2143704A1 (en) * | 2008-07-10 | 2010-01-13 | Rohm and Haas Company | An integrated process for preparing a carboxylic acid from an alkane |
| DE102008044946B4 (de) * | 2008-08-29 | 2022-06-15 | Evonik Superabsorber Gmbh | Einsatz von Schaumkörpern in Oxidations-Reaktoren zur Herstellung ungesättigter Carbonsäuren |
| JP5447895B2 (ja) * | 2009-12-01 | 2014-03-19 | ビーエーエスエフ ソシエタス・ヨーロピア | 自熱式の気相脱水素を実施するための反応器 |
| CN103889942B (zh) | 2011-10-18 | 2016-05-11 | 罗门哈斯公司 | 从丙烷和丙烯制备丙烯酸的方法 |
| FI130603B (en) | 2018-08-03 | 2023-12-08 | Neste Oyj | THE METHOD PRODUCES BIORENEWABLE PROPENE FROM OILS AND FATS |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2251364B2 (de) * | 1971-10-22 | 1975-07-03 | Asahi Glass Co. Ltd., Tokio | Verfahren zur Herstellung von Acrylsäure bzw. Methacrylsäure aus Acrolein bzw. Methacrolein |
| CA1217502A (en) * | 1982-04-14 | 1987-02-03 | Sargis Khoobiar | Conversion of alkanes to unsaturated aldehydes |
| EP0117146B1 (en) * | 1983-02-22 | 1986-12-30 | The Halcon Sd Group, Inc. | Conversion of propane to acrylic acid |
| US5198578A (en) * | 1986-07-17 | 1993-03-30 | Union Carbide Chemicals | Anhydrous diluents for the propylene oxidation reaction to acrolein and acrolein oxidation to acrylic acid |
| US5218146A (en) * | 1987-05-27 | 1993-06-08 | Nippon Shokubai Kagaku Kogyo Co., Ltd. | Process for production of acrylic acid |
| US5262547A (en) * | 1990-10-31 | 1993-11-16 | The Boc Group, Inc. | Process for the production of petrochemicals |
| US5466837A (en) * | 1993-09-30 | 1995-11-14 | The Boc Group, Inc. | Process for the production of hydrocarbon partial oxidation products |
-
1996
- 1996-03-04 EP EP96103300A patent/EP0731077B1/de not_active Expired - Lifetime
- 1996-03-04 DE DE59603316T patent/DE59603316D1/de not_active Expired - Lifetime
- 1996-03-04 ES ES96103300T patent/ES2139266T3/es not_active Expired - Lifetime
- 1996-03-06 TW TW85102734A patent/TW328534B/zh active
- 1996-03-07 JP JP8050643A patent/JPH08245494A/ja not_active Withdrawn
- 1996-03-08 CZ CZ96733A patent/CZ73396A3/cs unknown
- 1996-03-08 KR KR1019960006030A patent/KR960034158A/ko not_active Withdrawn
- 1996-03-08 CA CA002171417A patent/CA2171417A1/en not_active Abandoned
- 1996-03-08 US US08/618,440 patent/US5705684A/en not_active Expired - Fee Related
- 1996-03-09 SG SG1996006581A patent/SG40844A1/en unknown
- 1996-03-09 CN CN96105981A patent/CN1086690C/zh not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004526800A (ja) * | 2001-05-07 | 2004-09-02 | ビーエーエスエフ アクチェンゲゼルシャフト | プロパンの不均一系触媒部分酸化によるアクリル酸の製法 |
| JP2006500430A (ja) * | 2002-09-27 | 2006-01-05 | ビーエーエスエフ アクチェンゲゼルシャフト | プロピレンの少なくとも１種の部分酸化‐及び／又はアンモ酸化生成物の製法 |
| JP4783146B2 (ja) * | 2002-09-27 | 2011-09-28 | ビーエーエスエフ ソシエタス・ヨーロピア | プロピレンの少なくとも１種の部分酸化‐及び／又はアンモ酸化生成物の製法 |
| JP2009517358A (ja) * | 2005-11-24 | 2009-04-30 | ビーエーエスエフ ソシエタス・ヨーロピア | プロパンからのアクロレイン、又はアクリル酸、又はその混合物の製法 |
| JP2009520586A (ja) * | 2005-12-21 | 2009-05-28 | ビーエーエスエフ ソシエタス・ヨーロピア | 少なくとも１つの脱水素化される炭化水素の連続的不均一触媒部分脱水素化方法 |
| US8721996B2 (en) | 2005-12-21 | 2014-05-13 | Basf Se | Reactor for continuous heterogeneously catalyzed partial dehydrogenation of at least one hydrocarbon to be dehydrogenated |
| WO2009008422A1 (ja) * | 2007-07-11 | 2009-01-15 | Sumitomo Chemical Company, Limited | 混合ガスの製造方法および製造装置、ならびにエポキシ化合物の製造装置および製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR960034158A (ko) | 1996-10-22 |
| EP0731077A2 (de) | 1996-09-11 |
| CA2171417A1 (en) | 1996-09-11 |
| CZ73396A3 (en) | 1996-09-11 |
| CN1086690C (zh) | 2002-06-26 |
| ES2139266T3 (es) | 2000-02-01 |
| TW328534B (en) | 1998-03-21 |
| DE59603316D1 (de) | 1999-11-18 |
| EP0731077B1 (de) | 1999-10-13 |
| EP0731077A3 (enExample) | 1996-09-25 |
| CN1143068A (zh) | 1997-02-19 |
| US5705684A (en) | 1998-01-06 |
| SG40844A1 (enExample) | 1997-06-14 |
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