BE500700A - - Google Patents
Info
- Publication number
- BE500700A BE500700A BE500700DA BE500700A BE 500700 A BE500700 A BE 500700A BE 500700D A BE500700D A BE 500700DA BE 500700 A BE500700 A BE 500700A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- temperature
- atmospheres
- olefin
- pressure
- Prior art date
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 150000001336 alkenes Chemical class 0.000 claims description 19
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 18
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 14
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 13
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 13
- 238000006703 hydration reaction Methods 0.000 claims description 11
- 230000036571 hydration Effects 0.000 claims description 9
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 7
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 5
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 description 19
- 238000004519 manufacturing process Methods 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000007423 decrease Effects 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- XAYGUHUYDMLJJV-UHFFFAOYSA-Z decaazanium;dioxido(dioxo)tungsten;hydron;trioxotungsten Chemical compound [H+].[H+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O XAYGUHUYDMLJJV-UHFFFAOYSA-Z 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 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
- C07C29/03—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2
- C07C29/04—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE500700A true BE500700A (d) |
Family
ID=142725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE500700D BE500700A (d) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE500700A (d) |
-
0
- BE BE500700D patent/BE500700A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR2482953A1 (fr) | Procede d'hydrogenation selective d'une di-olefine dans un melange d'hydrocarbures renfermant au moins 4 atomes de carbone et contenant une olefine -a | |
EP0011042B1 (fr) | Procédé de préparation de l'acétaldéhyde | |
EP3074367B1 (fr) | Procede de production de 1,3-butadiène à partir d'une charge comprenant de l'éthanol | |
EP0022735A1 (fr) | Procédé de préparation de l'acétaldéhyde | |
EP3551603A1 (fr) | Procede pour eviter le depot de polymeres dans un procede de purification d'acide (meth)acrylique | |
FR2761984A1 (fr) | Procede d'oxydation d'hydrocarbures, d'alcools et/ou de cetones | |
EP1165481B1 (fr) | Procede d'oxydation de cycloalcanes, de cycloalcanols et/ou de cycloalcanones | |
BE500700A (d) | ||
FR2810904A1 (fr) | Procede d'oxydation d'hydrocarbures, d'alcools et/ou de cetones | |
EP2763945A1 (fr) | Procédé de préparation d'un mélange d'alcools | |
FR2490215A1 (fr) | Procede pour la preparation de melanges de methanol et d'alcools superieurs et melanges ainsi obtenus | |
FR2479186A1 (fr) | Procede pour la fabrication d'alcools ayant 2 a 4 atomes de carbone, de qualite essence, a partir de melanges aqueux les renfermant | |
EP0005296A1 (fr) | Procédé pour la fabrication de dichlorométhane | |
BE490555A (d) | ||
BE568457A (d) | ||
BE607984A (d) | ||
BE429113A (d) | ||
BE505098A (d) | ||
BE469882A (d) | ||
BE571721A (d) | ||
BE581022A (d) | ||
BE487957A (d) | ||
BE602008A (d) | ||
BE584446A (d) | ||
BE436625A (d) |