DD297574A5 - Katalysator fuer die katalytische gasphasenoxidation von olefinen zu ungesaettigten aldehyden - Google Patents
Katalysator fuer die katalytische gasphasenoxidation von olefinen zu ungesaettigten aldehyden Download PDFInfo
- Publication number
- DD297574A5 DD297574A5 DD90343951A DD34395190A DD297574A5 DD 297574 A5 DD297574 A5 DD 297574A5 DD 90343951 A DD90343951 A DD 90343951A DD 34395190 A DD34395190 A DD 34395190A DD 297574 A5 DD297574 A5 DD 297574A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- catalyst
- spray
- grain
- temperature
- extruded
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 106
- 230000003647 oxidation Effects 0.000 title abstract description 7
- 238000007254 oxidation reaction Methods 0.000 title abstract description 7
- 150000001299 aldehydes Chemical class 0.000 title abstract description 4
- 230000003197 catalytic effect Effects 0.000 title description 3
- 238000002360 preparation method Methods 0.000 claims abstract description 13
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 4
- 239000007921 spray Substances 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 29
- 239000000243 solution Substances 0.000 claims description 24
- 239000000725 suspension Substances 0.000 claims description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- 238000000137 annealing Methods 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 8
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 8
- 229910052753 mercury Inorganic materials 0.000 claims description 8
- 239000011148 porous material Substances 0.000 claims description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- 239000000314 lubricant Substances 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 5
- 229910052797 bismuth Inorganic materials 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 239000003208 petroleum Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 229920000609 methyl cellulose Polymers 0.000 claims description 4
- 239000001923 methylcellulose Substances 0.000 claims description 4
- 235000010981 methylcellulose Nutrition 0.000 claims description 4
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 230000001698 pyrogenic effect Effects 0.000 claims description 3
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 claims description 2
- 238000005520 cutting process Methods 0.000 claims description 2
- 230000008021 deposition Effects 0.000 claims description 2
- 239000003906 humectant Substances 0.000 claims description 2
- 230000001050 lubricating effect Effects 0.000 claims description 2
- 239000007764 o/w emulsion Substances 0.000 claims description 2
- 239000012266 salt solution Substances 0.000 claims description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229910004298 SiO 2 Inorganic materials 0.000 claims 1
- 239000007767 bonding agent Substances 0.000 claims 1
- 238000001354 calcination Methods 0.000 claims 1
- 238000005496 tempering Methods 0.000 claims 1
- 239000007789 gas Substances 0.000 abstract description 10
- 238000005299 abrasion Methods 0.000 abstract description 6
- 238000004519 manufacturing process Methods 0.000 abstract description 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract description 3
- 229910001882 dioxygen Inorganic materials 0.000 abstract description 3
- 239000012876 carrier material Substances 0.000 abstract description 2
- 230000035699 permeability Effects 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 36
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 32
- 238000003756 stirring Methods 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 14
- 238000001125 extrusion Methods 0.000 description 10
- 238000009792 diffusion process Methods 0.000 description 7
- 230000002349 favourable effect Effects 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 4
- 239000011149 active material Substances 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- KQEIJFWAXDQUPR-UHFFFAOYSA-N 2,4-diaminophenol;hydron;dichloride Chemical compound Cl.Cl.NC1=CC=C(O)C(N)=C1 KQEIJFWAXDQUPR-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000000889 atomisation Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000001307 helium Substances 0.000 description 3
- 229910052734 helium Inorganic materials 0.000 description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000013021 overheating Methods 0.000 description 3
- 235000010333 potassium nitrate Nutrition 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- RNAMYOYQYRYFQY-UHFFFAOYSA-N 2-(4,4-difluoropiperidin-1-yl)-6-methoxy-n-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine Chemical compound N1=C(N2CCC(F)(F)CC2)N=C2C=C(OCCCN3CCCC3)C(OC)=CC2=C1NC1CCN(C(C)C)CC1 RNAMYOYQYRYFQY-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000037237 body shape Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000002638 heterogeneous catalyst Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 239000011800 void material Substances 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/14—Phosphorus; Compounds thereof
- B01J27/186—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J27/188—Phosphorus; Compounds thereof with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with chromium, molybdenum, tungsten or polonium
- B01J27/19—Molybdenum
- B01J27/192—Molybdenum with bismuth
-
- 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
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3930533A DE3930533C1 (xx) | 1989-09-13 | 1989-09-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD297574A5 true DD297574A5 (de) | 1992-01-16 |
Family
ID=6389314
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD90343951A DD297574A5 (de) | 1989-09-13 | 1990-09-11 | Katalysator fuer die katalytische gasphasenoxidation von olefinen zu ungesaettigten aldehyden |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5082819A (xx) |
| EP (1) | EP0417722B1 (xx) |
| JP (1) | JP3145101B2 (xx) |
| CN (1) | CN1027045C (xx) |
| AT (1) | ATE97026T1 (xx) |
| AU (1) | AU624024B2 (xx) |
| BR (1) | BR9004581A (xx) |
| DD (1) | DD297574A5 (xx) |
| DE (2) | DE3930533C1 (xx) |
| DK (1) | DK0417722T3 (xx) |
| ES (1) | ES2022070T3 (xx) |
| MX (1) | MX174107B (xx) |
| ZA (1) | ZA907041B (xx) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| FR2670686B1 (fr) * | 1990-12-20 | 1994-08-12 | Rhone Poulenc Chimie | Composition catalytique pour la preparation d'aldehydes alpha,beta-insatures par oxydation d'olefines en phase gazeuse et procede d'oxydation. |
| FR2670685B1 (fr) * | 1990-12-20 | 1995-03-10 | Rhone Poulenc Chimie | Procede de preparation de catalyseurs enrobes a base de molybdates de bismuth et de fer dopes par du phosphore et du potassium. |
| IT1256156B (it) * | 1992-10-06 | 1995-11-29 | Montecatini Tecnologie Srl | Catalizzatore in granuli particolarmente per la deidrogenazione ossidativa di metanolo a formaldeide |
| IT1282267B1 (it) * | 1995-03-14 | 1998-03-16 | Montecatini Tecnologie Srl | Catalizzatori e supporti per catalizzatori ottenuti per pastigliatura |
| IT1283207B1 (it) * | 1996-03-08 | 1998-04-16 | Montecatini Tecnologie Srl | Catalizzatori per la deidrogenazione di etilbenzene a stirene |
| US6437193B1 (en) | 1997-07-15 | 2002-08-20 | E. I. Du Pont De Nemours And Company | Vapor phase oxidation of propylene to acrolein |
| US6281384B1 (en) | 1998-06-26 | 2001-08-28 | E. I. Du Pont Nemours And Company | Vapor phase catalytic oxidation of propylene to acrylic acid |
| TW511105B (en) | 1999-03-11 | 2002-11-21 | Murata Manufacturing Co | Method of firing magnetic core |
| EP1053789B1 (en) | 1999-05-21 | 2004-07-14 | Evc Technology Ag | Catalyst and oxychlorination process using it |
| EP1184077B1 (en) * | 2000-08-30 | 2005-10-19 | Haldor Topsoe A/S | Hydrotreating catalyst particles |
| JP4933709B2 (ja) * | 2001-09-26 | 2012-05-16 | 三菱レイヨン株式会社 | 不飽和カルボン酸合成用触媒の製造方法 |
| CN101066528B (zh) * | 2001-11-08 | 2010-09-29 | 三菱化学株式会社 | 复合氧化物催化剂及其制备方法 |
| EP2343124B1 (en) * | 2001-11-08 | 2021-01-06 | Mitsubishi Chemical Corporation | METHOD FOR PREPARATION of a COMPOSITE OXIDE CATALYST |
| EP1386664B1 (en) * | 2002-07-31 | 2016-05-11 | Ineos Technologies (Vinyls) Limited | A hollow parallelepiped pellet suitable as carrier of catalysts for selective exothermic reactions |
| DE10344149A1 (de) * | 2003-09-22 | 2004-04-08 | Basf Ag | Verfahren zur Herstellung von ringförmigen Vollkatalysatoren |
| MY144024A (en) * | 2003-09-22 | 2011-07-29 | Basf Ag | Preparation of annular unsupported catalysts |
| AU2003269532A1 (en) * | 2003-10-14 | 2005-04-27 | Lg Chem, Ltd. | A catalyst for gaseous partial oxidation of propylene and method for preparing the same |
| CN1697700A (zh) | 2003-12-04 | 2005-11-16 | 三菱化学株式会社 | 生产用于生产不饱和醛和不饱和羧酸催化剂的方法 |
| US7579297B2 (en) | 2003-12-18 | 2009-08-25 | Mitsubishi Rayon Co., Ltd. | Method for producing catalyst for production of unsaturated aldehyde and unsaturated carboxylic acid |
| US20070173662A1 (en) * | 2004-02-10 | 2007-07-26 | Mitsubishi Rayon Co., Ltd. | Catalyst for producing alpha, beta-unsaturated carboxylic acid and method for preparation thereof, and method for producing alpha, beta-unsaturated carboxylic acid |
| SG136121A1 (en) * | 2004-02-10 | 2007-10-29 | Mitsubishi Rayon Co | CATALYST FOR PRODUCING α, β-UNSATURATED CARBOXYLIC ACID AND METHOD FOR PREPARATION THEREOF, AND METHOD FOR PRODUCING α, β- UNSATURATED CARBOXYLIC ACID |
| JP4947756B2 (ja) * | 2005-03-25 | 2012-06-06 | 三菱レイヨン株式会社 | 不飽和アルデヒドおよび不飽和カルボン酸合成用触媒の製造方法、並びに不飽和アルデヒドおよび不飽和カルボン酸の製造方法 |
| US7732367B2 (en) * | 2005-07-25 | 2010-06-08 | Saudi Basic Industries Corporation | Catalyst for methacrolein oxidation and method for making and using same |
| US7649111B2 (en) * | 2005-07-25 | 2010-01-19 | Saudi Basic Industries Corporation | Catalyst for the oxidation of a mixed aldehyde feedstock to methacrylic acid and methods for making and using same |
| US7851397B2 (en) * | 2005-07-25 | 2010-12-14 | Saudi Basic Industries Corporation | Catalyst for methacrolein oxidation and method for making and using same |
| 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 |
| DE102006015710A1 (de) * | 2005-10-14 | 2007-04-26 | Degussa Gmbh | Mischoxidationskatalysatoren für die katalytische Gasphasenoxidation von Olefinen und Verfahren zu ihrer Herstellung |
| JP4749943B2 (ja) * | 2006-06-13 | 2011-08-17 | 東罐興業株式会社 | ホワイトアスパラ栽培用被覆フィルムとそれを用いた栽培用ハウス |
| 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 |
| CN102203040B (zh) * | 2008-11-06 | 2014-04-16 | 日本化药株式会社 | 甲基丙烯酸的制造方法及甲基丙烯酸制造用催化剂 |
| JP2011102249A (ja) * | 2009-11-10 | 2011-05-26 | Nippon Shokubai Co Ltd | アクリル酸の製造方法 |
| DE102010052126A1 (de) * | 2010-11-22 | 2012-05-24 | Süd-Chemie AG | Katalysatorformkörper für durchströmte Festbettreaktoren |
| JP5394457B2 (ja) * | 2011-09-02 | 2014-01-22 | 三菱レイヨン株式会社 | 不飽和アルデヒドおよび不飽和カルボン酸合成用触媒、その製造方法、並びに不飽和アルデヒドおよび不飽和カルボン酸の製造方法 |
| US8921257B2 (en) | 2011-12-02 | 2014-12-30 | Saudi Basic Industries Corporation | Dual function partial oxidation catalyst for propane to acrylic acid conversion |
| WO2013106771A2 (en) | 2012-01-13 | 2013-07-18 | Siluria Technologies, Inc. | Process for separating hydrocarbon compounds |
| US8722940B2 (en) | 2012-03-01 | 2014-05-13 | Saudi Basic Industries Corporation | High molybdenum mixed metal oxide catalysts for the production of unsaturated aldehydes from olefins |
| CN103524312A (zh) * | 2012-07-03 | 2014-01-22 | 中国石油化工股份有限公司 | 制备甲基丙烯醛的方法 |
| US9969660B2 (en) | 2012-07-09 | 2018-05-15 | Siluria Technologies, Inc. | Natural gas processing and systems |
| CA2893948C (en) | 2012-12-07 | 2022-12-06 | Siluria Technologies, Inc. | Integrated processes and systems for conversion of methane to ethylene and conversion of ethylene to higher hydrocarbon products |
| EP3074119B1 (en) | 2013-11-27 | 2019-01-09 | Siluria Technologies, Inc. | Reactors and systems for oxidative coupling of methane |
| CN106068323B (zh) | 2014-01-08 | 2019-09-06 | 希路瑞亚技术公司 | 乙烯成液体的系统和方法 |
| US10377682B2 (en) | 2014-01-09 | 2019-08-13 | Siluria Technologies, Inc. | Reactors and systems for oxidative coupling of methane |
| AU2015204709B2 (en) | 2014-01-09 | 2019-08-15 | Lummus Technology Llc | Oxidative coupling of methane implementations for olefin production |
| CN107405609B (zh) * | 2015-02-27 | 2020-09-29 | 日本化药株式会社 | 用于制造不饱和醛和/或不饱和羧酸的催化剂及其制造方法以及不饱和醛和/或不饱和羧酸的制造方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2941007A (en) * | 1957-06-10 | 1960-06-14 | Standard Oil Co | Process for the oxidation of olefins |
| FR2016707A1 (xx) * | 1968-08-31 | 1970-05-08 | Degussa | |
| JPS5498717A (en) * | 1978-01-17 | 1979-08-03 | Nippon Zeon Co Ltd | Preparation of unsaturated carboxylic acid |
| DE3125061C2 (de) * | 1981-06-26 | 1984-03-15 | Degussa Ag, 6000 Frankfurt | Verfahren zur Herstellung von Acrolein bzw. Methacrolein durch katalytische Oxidation von Propylen bzw. Isobutylen oder tertiär-Butanol in sauerstoffhaltigen Gasgemischen |
| JPS58119346A (ja) * | 1982-01-06 | 1983-07-15 | Nippon Shokubai Kagaku Kogyo Co Ltd | プロピレン酸化用触媒 |
| JPS5946132A (ja) * | 1982-09-06 | 1984-03-15 | Nippon Shokubai Kagaku Kogyo Co Ltd | メタクロレイン合成用触媒 |
| US4537874A (en) * | 1982-10-22 | 1985-08-27 | Nippon Shokubai Kagaku Kogyo Co Ltd | Catalyst for production of unsaturated aldehydes |
| US4510261A (en) * | 1983-10-17 | 1985-04-09 | W. R. Grace & Co. | Catalyst with high geometric surface area |
| EP0296285B1 (en) * | 1987-06-24 | 1992-07-29 | The Dow Chemical Company | A dehydrogenation catalyst having improved moisture stability and a process for making the same |
| SU1665870A3 (ru) * | 1986-03-24 | 1991-07-23 | Мицубиси Петрокемикал Компани Лимитед (Фирма) | Способ приготовлени окисного катализатора дл окислени пропилена |
| DE3867249D1 (de) * | 1987-02-17 | 1992-02-13 | Nippon Catalytic Chem Ind | Katalysator zur oxydation von olefin oder tertiaerem alkohol und verfahren zu seiner herstellung. |
| DE3740271A1 (de) * | 1987-11-27 | 1989-06-01 | Basf Ag | Verfahren zur herstellung einer fuer die gasphasenoxidation von propylen zu acrolein und acrylsaeure katalytisch aktiven masse |
| DE3827639A1 (de) * | 1988-08-16 | 1990-02-22 | Basf Ag | Katalysator fuer die oxidation und ammonoxidation von (alpha),ss-ungesaettigten kohlenwasserstoffen |
-
1989
- 1989-09-13 DE DE3930533A patent/DE3930533C1/de not_active Expired - Lifetime
-
1990
- 1990-09-04 ZA ZA907041A patent/ZA907041B/xx unknown
- 1990-09-11 EP EP90117464A patent/EP0417722B1/de not_active Expired - Lifetime
- 1990-09-11 DE DE90117464T patent/DE59003442D1/de not_active Expired - Fee Related
- 1990-09-11 DD DD90343951A patent/DD297574A5/de not_active IP Right Cessation
- 1990-09-11 ES ES90117464T patent/ES2022070T3/es not_active Expired - Lifetime
- 1990-09-11 DK DK90117464.9T patent/DK0417722T3/da active
- 1990-09-11 AT AT90117464T patent/ATE97026T1/de not_active IP Right Cessation
- 1990-09-12 AU AU62459/90A patent/AU624024B2/en not_active Ceased
- 1990-09-12 MX MX022353A patent/MX174107B/es unknown
- 1990-09-13 CN CN90107664A patent/CN1027045C/zh not_active Expired - Fee Related
- 1990-09-13 BR BR909004581A patent/BR9004581A/pt not_active IP Right Cessation
- 1990-09-13 JP JP24137590A patent/JP3145101B2/ja not_active Expired - Fee Related
- 1990-09-13 US US07/581,702 patent/US5082819A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| MX174107B (es) | 1994-04-21 |
| JP3145101B2 (ja) | 2001-03-12 |
| ATE97026T1 (de) | 1993-11-15 |
| ZA907041B (en) | 1991-06-26 |
| CN1027045C (zh) | 1994-12-21 |
| DE3930533C1 (xx) | 1991-05-08 |
| ES2022070A4 (es) | 1991-12-01 |
| AU624024B2 (en) | 1992-05-28 |
| DE59003442D1 (de) | 1993-12-16 |
| EP0417722B1 (de) | 1993-11-10 |
| DK0417722T3 (da) | 1996-04-22 |
| AU6245990A (en) | 1991-03-21 |
| BR9004581A (pt) | 1991-09-10 |
| US5082819A (en) | 1992-01-21 |
| JPH03109946A (ja) | 1991-05-09 |
| EP0417722A1 (de) | 1991-03-20 |
| CN1050340A (zh) | 1991-04-03 |
| ES2022070T3 (es) | 1994-03-01 |
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