ES461521A1 - Mejoras introducidas en un metodo de coproduccion de estire-no y de un oxido de alquileno inferior. - Google Patents
Mejoras introducidas en un metodo de coproduccion de estire-no y de un oxido de alquileno inferior.Info
- Publication number
- ES461521A1 ES461521A1 ES461521A ES461521A ES461521A1 ES 461521 A1 ES461521 A1 ES 461521A1 ES 461521 A ES461521 A ES 461521A ES 461521 A ES461521 A ES 461521A ES 461521 A1 ES461521 A1 ES 461521A1
- Authority
- ES
- Spain
- Prior art keywords
- stream
- alkylene oxide
- styrene
- lower alkylene
- containg
- 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.)
- Expired
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 title abstract 8
- 125000002947 alkylene group Chemical group 0.000 title abstract 4
- 239000007795 chemical reaction product Substances 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 238000007086 side reaction Methods 0.000 title 1
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 abstract 4
- GQNOPVSQPBUJKQ-UHFFFAOYSA-N 1-hydroperoxyethylbenzene Chemical compound OOC(C)C1=CC=CC=C1 GQNOPVSQPBUJKQ-UHFFFAOYSA-N 0.000 abstract 2
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 abstract 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 239000012535 impurity Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000011787 zinc oxide Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/19—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic hydroperoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/40—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals
- C07C15/42—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals monocyclic
- C07C15/44—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts substituted by unsaturated carbon radicals monocyclic the hydrocarbon substituent containing a carbon-to-carbon double bond
- C07C15/46—Styrene; Ring-alkylated styrenes
-
- 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
-
- 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
- C07C29/143—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 ketones
- C07C29/145—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 ketones with hydrogen or hydrogen-containing gases
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Abstract
Mejoras introducidas en un método de coproducción de estireno y de un óxido de alquileno inferior, en el cual una corriente de etilbenceno se oxida en hidroperóxido de etilbenceno, dicho hidroperóxido de etilbenceno se utiliza para reaccionar con una olefina para preparar una corriente de un óxido de alquileno inferior, una corriente que contiene metilbencilalcohol se hace pasar a través de una zona de deshidratación para preparar vapor y estireno, una corriente de acetofenona que contiene varias impurezas constituye un subproducto, una corriente conteniendo metilbencilalcohol se prepara mediante hidrogenación de una corriente conteniendo acetofenona conjuntamente con hidrógeno sobre una capa de partículas de catalizador que consiste en óxido de cinc que soporta cantidades catalíticas de cobre a una temperatura superior a la temperatura ambiente y una presión superior a la presión atmosférica, dicho estireno y dicho óxido de alquileno inferior se recuperan por separado como coproductos de la operación.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71576976A | 1976-08-19 | 1976-08-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES461521A1 true ES461521A1 (es) | 1978-06-16 |
Family
ID=24875404
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES461521A Expired ES461521A1 (es) | 1976-08-19 | 1977-08-10 | Mejoras introducidas en un metodo de coproduccion de estire-no y de un oxido de alquileno inferior. |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS5325503A (es) |
| ES (1) | ES461521A1 (es) |
| NL (1) | NL7709128A (es) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004085354A3 (en) * | 2003-03-28 | 2005-03-17 | Shell Int Research | Process for the hydrogenation of alkylaryl ketones |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4653316A (en) * | 1986-03-14 | 1987-03-31 | Kabushiki Kaisha Komatsu Seisakusho | Apparatus mounted on vehicles for detecting road surface conditions |
| US5171868A (en) * | 1992-04-15 | 1992-12-15 | Arco Chemical Technology, L.P. | Epoxidate treatment |
| SG98016A1 (en) * | 2000-01-12 | 2003-08-20 | Sumitomo Chemical Co | Process for producing alpha-phenylethyl alcohol |
-
1977
- 1977-08-10 ES ES461521A patent/ES461521A1/es not_active Expired
- 1977-08-18 NL NL7709128A patent/NL7709128A/xx not_active Application Discontinuation
- 1977-08-19 JP JP9940177A patent/JPS5325503A/ja active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004085354A3 (en) * | 2003-03-28 | 2005-03-17 | Shell Int Research | Process for the hydrogenation of alkylaryl ketones |
| US6939996B2 (en) | 2003-03-28 | 2005-09-06 | Shell Oil Company | Process for the hydrogenation of alkylaryl ketones |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7709128A (nl) | 1978-02-21 |
| JPS5325503A (en) | 1978-03-09 |
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