BE545326A - - Google Patents
Info
- Publication number
- BE545326A BE545326A BE545326DA BE545326A BE 545326 A BE545326 A BE 545326A BE 545326D A BE545326D A BE 545326DA BE 545326 A BE545326 A BE 545326A
- Authority
- BE
- Belgium
- Prior art keywords
- promoters
- water
- catalysts
- amount
- catalyst
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 claims description 26
- 150000001336 alkenes Chemical class 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 10
- 229910001930 tungsten oxide Inorganic materials 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 6
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims description 4
- VVRQVWSVLMGPRN-UHFFFAOYSA-N oxotungsten Chemical class [W]=O VVRQVWSVLMGPRN-UHFFFAOYSA-N 0.000 claims description 4
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 238000006555 catalytic reaction Methods 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 239000000741 silica gel Substances 0.000 claims description 2
- 229910002027 silica gel Inorganic materials 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 238000007792 addition Methods 0.000 claims 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 6
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- -1 methylene, propylene Chemical group 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000006187 pill Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE545326A true BE545326A (enExample) |
Family
ID=173008
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE545326D BE545326A (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE545326A (enExample) |
-
0
- BE BE545326D patent/BE545326A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1874720B1 (fr) | Procede de preparation d'acide acrylique a partir de glycerol | |
| FR2606013A1 (fr) | Procede et catalyseur perfectionnes pour l'hydrogenation d'aldehydes | |
| FR2458524A1 (fr) | Procede d'hydrogenation selective d'une fraction d'hydrocarbures renfermant 2 ou 3 atomes de carbone par molecule | |
| FR2523121A1 (fr) | Procede pour la preparation d'ethers tertio-butyl alkyliques en presence de butadiene | |
| EP4594289A1 (fr) | Procede de fabrication d'acide (meth)acrylique | |
| FR2945810A1 (fr) | Procede de production d'un support dialcoxymagnesium pour un catalyseur destine a la polymerisation d'olefines, procede de production d'un catalyseur destine a la polymerisation d'olefines l'utilisant et procede de polymerisation d'une olefine l'utilisant | |
| EP0668257A1 (fr) | Catalyseur et procédé d'hydrogénation du benzène utilisant ledit catalyseur | |
| BE545326A (enExample) | ||
| EP1702025B1 (fr) | PROCEDE DE TRANSFORMATION D’UN GAZ DE SYNTHESE EN HYDROCARBURES EN PRESENCE DE SIC BETA ET EFFLUENT DE CE PROCEDE | |
| FR3108532A1 (fr) | Production d’alcool allylique à partir de glycérol en utilisant un catalyseur réutilisable à base de rhénium | |
| CN1781893A (zh) | 稳定化的羟基新戊醛 | |
| CN1134410A (zh) | 异丙醇的制备方法 | |
| FR2517306A1 (fr) | Procede de preparation catalytique de carbonates d'alkylenes | |
| EP0018896B1 (fr) | Procédé de fabrication de perborate de sodium | |
| CN118666641B (zh) | 钙法三羟甲基丙烷高效缩合制备方法 | |
| FR2495138A1 (fr) | Procede de preparation de l'acide gloxylique | |
| BE1006062A3 (fr) | Procede pour la preparation en marche discontinue des carbonates d'alcoyle et d'aryle. | |
| EP4638398A1 (fr) | Conversion d'une charge hydrocarbonee issue de la biomasse pour produire de l'acide adipique | |
| BE575854A (enExample) | ||
| BE620845A (enExample) | ||
| BE495894A (enExample) | ||
| BE601720A (enExample) | ||
| FR2597861A1 (fr) | Nouveau procede de preparation du dihydromyrcenol | |
| BE505098A (enExample) | ||
| BE502024A (enExample) |