GB733753A - Process for carrying out hydrocarbon reactions accelerated by catalysts of an acid nature - Google Patents
Process for carrying out hydrocarbon reactions accelerated by catalysts of an acid natureInfo
- Publication number
- GB733753A GB733753A GB26227/53A GB2622753A GB733753A GB 733753 A GB733753 A GB 733753A GB 26227/53 A GB26227/53 A GB 26227/53A GB 2622753 A GB2622753 A GB 2622753A GB 733753 A GB733753 A GB 733753A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butene
- catalyst
- groups
- propene
- alkylation
- 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
- 239000003054 catalyst Substances 0.000 title abstract 6
- 238000006243 chemical reaction Methods 0.000 title abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 title 1
- 239000002253 acid Substances 0.000 title 1
- 229930195733 hydrocarbon Natural products 0.000 title 1
- 150000002430 hydrocarbons Chemical class 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 6
- 150000001336 alkenes Chemical class 0.000 abstract 6
- 229920005989 resin Polymers 0.000 abstract 6
- 239000011347 resin Substances 0.000 abstract 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 abstract 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 4
- 239000000499 gel Substances 0.000 abstract 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 230000029936 alkylation Effects 0.000 abstract 3
- 238000005804 alkylation reaction Methods 0.000 abstract 3
- 238000007334 copolymerization reaction Methods 0.000 abstract 3
- 238000006116 polymerization reaction Methods 0.000 abstract 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001335 aliphatic alkanes Chemical class 0.000 abstract 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 abstract 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 150000001993 dienes Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 239000001282 iso-butane Substances 0.000 abstract 2
- 229910052755 nonmetal Inorganic materials 0.000 abstract 2
- 150000002843 nonmetals Chemical class 0.000 abstract 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 abstract 1
- DFVOXRAAHOJJBN-UHFFFAOYSA-N 6-methylhept-1-ene Chemical compound CC(C)CCCC=C DFVOXRAAHOJJBN-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 150000001450 anions Chemical group 0.000 abstract 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 abstract 1
- 238000006471 dimerization reaction Methods 0.000 abstract 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000005342 ion exchange Methods 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229920002521 macromolecule Polymers 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 230000001376 precipitating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/56—Addition to acyclic hydrocarbons
- C07C2/58—Catalytic processes
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
- B01J31/08—Ion-exchange resins
-
- 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
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
- B01J31/08—Ion-exchange resins
- B01J31/10—Ion-exchange resins sulfonated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
- C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
- C07C2/06—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
- C07C2/08—Catalytic processes
- C07C2/26—Catalytic processes with hydrides or organic compounds
- C07C2/28—Catalytic processes with hydrides or organic compounds with ion-exchange resins
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/10—Polymerisation reactions involving at least dual use catalysts, e.g. for both oligomerisation and polymerisation
- B01J2231/12—Olefin polymerisation or copolymerisation
-
- 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
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
- B01J2231/32—Addition reactions to C=C or C-C triple bonds
- B01J2231/323—Hydrometalation, e.g. bor-, alumin-, silyl-, zirconation or analoguous reactions like carbometalation, hydrocarbation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
- C07C2531/08—Ion-exchange resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL733753X | 1952-09-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB733753A true GB733753A (en) | 1955-07-20 |
Family
ID=19820350
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB26227/53A Expired GB733753A (en) | 1952-09-25 | 1953-09-23 | Process for carrying out hydrocarbon reactions accelerated by catalysts of an acid nature |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE523001A (enrdf_load_stackoverflow) |
| FR (1) | FR1083962A (enrdf_load_stackoverflow) |
| GB (1) | GB733753A (enrdf_load_stackoverflow) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2843642A (en) * | 1956-09-14 | 1958-07-15 | American Oil Co | Alkylation process |
| US3017441A (en) * | 1957-12-10 | 1962-01-16 | Sinclair Refining Co | Process for nuctear alkylation of aromatic hydrocarbons |
| DE1194398B (de) * | 1960-07-14 | 1965-06-10 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des Isobutens |
| DE1194399B (de) * | 1962-08-10 | 1965-06-10 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des n-Butens |
| DE1199761B (de) * | 1961-09-21 | 1965-09-02 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des Isobutens |
| DE1213837B (de) * | 1961-12-20 | 1966-04-07 | Bayer Ag | Verfahren zur Herstellung von Oligomeren aus Butenen |
| US3370101A (en) * | 1963-11-19 | 1968-02-20 | Atlantic Richfield Co | Cocatalyst system for organic reactions |
| DE1287564B (de) * | 1961-09-26 | 1969-01-23 | Mobil Oil Corp | Verfahren zur katalytischen Alkylierung von aromatischen Kohlenwasserstoffen |
| US4056578A (en) * | 1976-03-04 | 1977-11-01 | Shell Oil Company | Isoparaffin-olefin alkylation process using a supported perfluorinated polymer catalyst |
| US4180695A (en) * | 1976-03-04 | 1979-12-25 | Shell Oil Company | Isoparaffin alkylation process using an unsupported perfluorinated polymer catalyst |
| US4188308A (en) * | 1976-02-23 | 1980-02-12 | Varen Technology | Conversion of pendant sulfonate groups to sulfonic acid groups on perfluorvinylether-tetrafluoroethylene copolymer catalysts |
| US4317949A (en) * | 1976-02-23 | 1982-03-02 | Varen Technology | Alkylation process and apparatus useful therein |
| EP0565197A1 (en) * | 1992-04-08 | 1993-10-13 | Shell Internationale Researchmaatschappij B.V. | Process for upgrading a paraffinic feedstock |
| CN112745183A (zh) * | 2019-10-31 | 2021-05-04 | 中国石油化工股份有限公司 | 一种低异丁烯含量的c4齐聚合成异辛烯的方法 |
-
0
- BE BE523001D patent/BE523001A/xx unknown
- FR FR1083962D patent/FR1083962A/fr not_active Expired
-
1953
- 1953-09-23 GB GB26227/53A patent/GB733753A/en not_active Expired
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2843642A (en) * | 1956-09-14 | 1958-07-15 | American Oil Co | Alkylation process |
| US3017441A (en) * | 1957-12-10 | 1962-01-16 | Sinclair Refining Co | Process for nuctear alkylation of aromatic hydrocarbons |
| DE1194398B (de) * | 1960-07-14 | 1965-06-10 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des Isobutens |
| DE1199761B (de) * | 1961-09-21 | 1965-09-02 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des Isobutens |
| DE1287564B (de) * | 1961-09-26 | 1969-01-23 | Mobil Oil Corp | Verfahren zur katalytischen Alkylierung von aromatischen Kohlenwasserstoffen |
| DE1213837B (de) * | 1961-12-20 | 1966-04-07 | Bayer Ag | Verfahren zur Herstellung von Oligomeren aus Butenen |
| DE1194399B (de) * | 1962-08-10 | 1965-06-10 | Bayer Ag | Verfahren zur Herstellung von Oligomeren des n-Butens |
| US3370101A (en) * | 1963-11-19 | 1968-02-20 | Atlantic Richfield Co | Cocatalyst system for organic reactions |
| US4188308A (en) * | 1976-02-23 | 1980-02-12 | Varen Technology | Conversion of pendant sulfonate groups to sulfonic acid groups on perfluorvinylether-tetrafluoroethylene copolymer catalysts |
| US4317949A (en) * | 1976-02-23 | 1982-03-02 | Varen Technology | Alkylation process and apparatus useful therein |
| US4056578A (en) * | 1976-03-04 | 1977-11-01 | Shell Oil Company | Isoparaffin-olefin alkylation process using a supported perfluorinated polymer catalyst |
| US4180695A (en) * | 1976-03-04 | 1979-12-25 | Shell Oil Company | Isoparaffin alkylation process using an unsupported perfluorinated polymer catalyst |
| EP0565197A1 (en) * | 1992-04-08 | 1993-10-13 | Shell Internationale Researchmaatschappij B.V. | Process for upgrading a paraffinic feedstock |
| CN112745183A (zh) * | 2019-10-31 | 2021-05-04 | 中国石油化工股份有限公司 | 一种低异丁烯含量的c4齐聚合成异辛烯的方法 |
| CN112745183B (zh) * | 2019-10-31 | 2022-08-12 | 中国石油化工股份有限公司 | 一种低异丁烯含量的c4齐聚合成异辛烯的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| BE523001A (enrdf_load_stackoverflow) | 1900-01-01 |
| FR1083962A (enrdf_load_stackoverflow) | 1955-01-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB733753A (en) | Process for carrying out hydrocarbon reactions accelerated by catalysts of an acid nature | |
| US4100220A (en) | Dimerization of isobutene | |
| US2181640A (en) | Process and products relating to production of valuable hydrocarbons | |
| US3862258A (en) | Isoparaffin-olefin alkylation with added water and with a complex of a macroreticular acid cation exchange resin and bf{11 | |
| US5663474A (en) | Alkylation process using hydrogen fluoride-containing alkylation catalysts | |
| US4087471A (en) | Fixed bed process for the production of t-butanol | |
| MXPA02005762A (es) | Oligomerizacion de olefina selectiva. | |
| US4162233A (en) | Isomerization-alkylation systems comprising a Gr. III A Lewis acid and a non-reactive aprotic solvent | |
| Sun et al. | An extremely active solid acid catalyst, Nafion resin/silica composite, for the Friedel− Crafts benzylation of benzene and p-xylene with benzyl alcohol | |
| US4229611A (en) | Isomerization alkylation systems | |
| CA1072129A (en) | Process for the alkylation of light paraffins with lower olefins | |
| US4056578A (en) | Isoparaffin-olefin alkylation process using a supported perfluorinated polymer catalyst | |
| SA96170115B1 (ar) | عملية انتاج مشترك لاثيرات وهيدروكربونات ذات عدد او كتيني مرتفع | |
| Uematsu | The Isomerization of n-Butenes over Acidic Ion-exchange Resin | |
| US3116346A (en) | Alkylation process | |
| US2803667A (en) | Production of alcohols and ethers | |
| US4180695A (en) | Isoparaffin alkylation process using an unsupported perfluorinated polymer catalyst | |
| US4123379A (en) | Production of very strongly acidic solids for hydrocarbon conversions | |
| US2355868A (en) | Catalytic hydrocarbon reactions and catalysts therefor | |
| US2313103A (en) | Alkylation of paraffin hydrocarbons | |
| CA1091606A (en) | Combination isomerization - alkylation process | |
| US2421946A (en) | Polymerization of olefinic hydrocarbons | |
| US2322664A (en) | Production of motor fuels | |
| US2450039A (en) | Isomerization process | |
| US2090905A (en) | Polymerization of olefins |