GB791317A - Improvements in or relating to transalkylation processes - Google Patents
Improvements in or relating to transalkylation processesInfo
- Publication number
- GB791317A GB791317A GB21865/55A GB2186555A GB791317A GB 791317 A GB791317 A GB 791317A GB 21865/55 A GB21865/55 A GB 21865/55A GB 2186555 A GB2186555 A GB 2186555A GB 791317 A GB791317 A GB 791317A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzene
- benzenes
- diisopropyl
- mixture
- per cent
- 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
- 238000000034 method Methods 0.000 title abstract 3
- 238000010555 transalkylation reaction Methods 0.000 title abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 18
- 239000000203 mixture Substances 0.000 abstract 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 4
- 239000003054 catalyst Substances 0.000 abstract 4
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 4
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 abstract 3
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical class CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 2
- 150000004996 alkyl benzenes Chemical class 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001555 benzenes Chemical class 0.000 abstract 2
- 229910052681 coesite Inorganic materials 0.000 abstract 2
- 229910052906 cristobalite Inorganic materials 0.000 abstract 2
- 238000004821 distillation Methods 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 239000000377 silicon dioxide Substances 0.000 abstract 2
- 235000012239 silicon dioxide Nutrition 0.000 abstract 2
- 229910052682 stishovite Inorganic materials 0.000 abstract 2
- 229910052905 tridymite Inorganic materials 0.000 abstract 2
- LGXAANYJEHLUEM-UHFFFAOYSA-N 1,2,3-tri(propan-2-yl)benzene Chemical class CC(C)C1=CC=CC(C(C)C)=C1C(C)C LGXAANYJEHLUEM-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 229910052593 corundum Inorganic materials 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 150000004760 silicates Chemical class 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- -1 which is recycled Chemical compound 0.000 abstract 1
- 229910001845 yogo sapphire Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/08—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
- C07C6/12—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring
- C07C6/126—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring of more than one hydrocarbon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Abstract
A transalkylation process comprises passing one or more alkylbenzenes having at least two alkyl groups, together with benzene and/or a monoalkyl benzene, in the liquid phase over a silicate catalyst containing, in combined form, one or more of the metals Al, Mg and Zr and which is of natural or synthetic origin. Catalysts referred to are silicates containing SiO2 and oxides of Al, Zr, Mg, and optionally also of Ca, Na and K in combined form; oxides of hydrogen, carbon and sulphur in bound form may also be present. A catalyst containing 85-90 per cent SiO2 and 15-10 per cent Al2O3 is specified. The catalyst may contain less than 3.5 per cent of water. The reaction temperature may be 160-350 DEG C., and the pressure 10-80 atm. The process may yield a considerable amount of p-diisopropyl benzene and be substantially free from the o-isomer. The alkylbenzenes having at least two alkyl groups may be tri- or tetra-isopropyl-benzenes. Cumene may be alkylated with a mixture of propene and propane and a mixture of ortho and meta-di-isomers obtained by distillation of the reaction product transalkylated with benzene. The bottom product of the distillation consists of a mixture of para-diisopropyl benzene, and higher alkylated products which are separated and passed to the transalkylator. The reaction mixture from the transalkylator consists of benzene, which is recycled, cumene, which is recycled to the alkylation zone, diisopropyl benzenes and higher alkylated benzenes. In the examples, mixtures of tri-isopropyl benzenes and benzene; and diisopropyl benzenes and benzene, with or without triisopropyl benzenes, are transalkylated to obtain an increased proportion of p-diisopropyl benzene in the mixtures.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL791317X | 1954-07-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB791317A true GB791317A (en) | 1958-02-26 |
Family
ID=19834416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21865/55A Expired GB791317A (en) | 1954-07-30 | 1955-07-28 | Improvements in or relating to transalkylation processes |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB791317A (en) |
-
1955
- 1955-07-28 GB GB21865/55A patent/GB791317A/en not_active Expired
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2939890A (en) | Alkylation of aromatic hydrocarbons | |
| US2721886A (en) | Catalyzed condensation of aromatic compounds with unsaturated organic compounds | |
| US3428701A (en) | Alkylation-transalkylation process | |
| US3205277A (en) | Alkylation-transalkylation process | |
| GB791317A (en) | Improvements in or relating to transalkylation processes | |
| GB1170871A (en) | Improved process for aromatic alkylation | |
| US2848514A (en) | Process for producing diisopropyl benzenes | |
| GB809908A (en) | A continuous process for preparing meta di-isopropylbenzene | |
| US3068301A (en) | Alkylation of aromatic hydrocarbons | |
| US3054836A (en) | Alkylation of aromatic hydrocarbons | |
| US2971992A (en) | Alkylation of aromatic hydrocarbons | |
| US3054835A (en) | Alkylation of aromatic hydrocarbons | |
| US2767230A (en) | Alkylation process | |
| GB786305A (en) | A process for isomerizing dialkyl benzenes in the liquid phase | |
| US2329858A (en) | Treatment of hydrocarbons | |
| US3293315A (en) | Alkylation process and catalyst therefor | |
| GB794570A (en) | Improvements in and relating to the alkylation of aromatic hydrocarbons | |
| US3417148A (en) | Alkylation process | |
| US2817687A (en) | Preparation of m- and p-diisopropyl-benzene | |
| US2849505A (en) | Alkylation catalyst comprising a tin halide and metallic aluminum | |
| US2855430A (en) | Process for the preparation of diisopropylbenzene | |
| GB799186A (en) | A continuous process for catalytically alkylating aromatic hydrocarbons and alkylatable hydroxy derivatives thereof in the liquid phase by means of olefins | |
| US2441095A (en) | Conversion of alkyl aromatic hydrocarbons into alkenyl aromatic hydrocarbons | |
| GB749186A (en) | Process for preparing ú-di-isopropyl benzene and terephthalic acid | |
| US3183233A (en) | Alkylation-transalkylation process |