MY189165A - Polystyrene sulfonic acid resin catalyst, preparation method therefor and use thereof - Google Patents
Polystyrene sulfonic acid resin catalyst, preparation method therefor and use thereofInfo
- Publication number
- MY189165A MY189165A MYPI2018701378A MYPI2018701378A MY189165A MY 189165 A MY189165 A MY 189165A MY PI2018701378 A MYPI2018701378 A MY PI2018701378A MY PI2018701378 A MYPI2018701378 A MY PI2018701378A MY 189165 A MY189165 A MY 189165A
- Authority
- MY
- Malaysia
- Prior art keywords
- sulfonic acid
- acid resin
- isobutylene
- catalyst
- polystyrene sulfonic
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title abstract 7
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 title abstract 6
- 229940005642 polystyrene sulfonic acid Drugs 0.000 title abstract 6
- 239000011347 resin Substances 0.000 title abstract 6
- 229920005989 resin Polymers 0.000 title abstract 6
- 238000002360 preparation method Methods 0.000 title abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 7
- 239000002184 metal Substances 0.000 abstract 7
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 abstract 5
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 230000018044 dehydration Effects 0.000 abstract 4
- 238000006297 dehydration reaction Methods 0.000 abstract 4
- 238000006384 oligomerization reaction Methods 0.000 abstract 4
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 abstract 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 230000001502 supplementing effect Effects 0.000 abstract 1
Classifications
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- 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
- B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
- B01J31/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
-
- 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
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0219—Coating the coating containing organic compounds
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0225—Coating of metal substrates
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0215—Coating
- B01J37/0228—Coating in several steps
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/12—Oxidising
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/24—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by elimination of water
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C07C11/08—Alkenes with four carbon atoms
- C07C11/09—Isobutene
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/12—Acetic acid esters
- C07C69/14—Acetic acid esters of monohydroxylic compounds
-
- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00008—Controlling the process
- B01J2208/00539—Pressure
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- 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
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/06—Details of tube reactors containing solid particles
- B01J2208/065—Heating or cooling the reactor
-
- 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
- B01J2231/20—Olefin oligomerisation or telomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24
- C07C2531/28—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups C07C2531/02 - C07C2531/24 of the platinum group metals, iron group metals or copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
A polystyrene sulfonic acid resin catalyst and a preparation method therefor. The catalyst is separately used for performing dehydration of tertiary butyl alcohol (TBA) and isobutylene oligomerization to cogenerate isobutylene and diisobutylene (DIB). The catalyst comprises a polystyrene sulfonic acid resin, a metal, and a metal sulfate. The metal contains two parts: metal coated with the polystyrene sulfonic acid resin, and metal not coated with the polystyrene sulfonic acid resin. The metal sulfate is formed by converting the exposed surface of the metal not coated with the polystyrene sulfonic acid resin in the catalyst. When the catalyst is separately used in the dehydration of TBA and the isobutylene oligomerization, due to the high thermal conductivity of the catalyst, the two reactions are coupled, thus supplementing energy required by the dehydration of TBA and greatly reducing the hot-spot temperature of the bed layer of the isobutylene oligomerization. In the reaction, the conversion rate per pass of the dehydration of TBA may be 40% or more, and the selectivity of isobutylene is 99% or more. Moreover, there is no need to add inhibitor when the isobutylene oligomerization is catalyzed, because even if is isobutylene with a concentration greater than 80 wt% is used as a raw material, the selectivity of DIB is still 80% or more, and the conversion rate per pass is 90% or more. (Figure 1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610393945.3A CN107457001B (en) | 2016-06-03 | 2016-06-03 | A kind of polystyrene sulfonic acid resin catalyst and its preparation method and application |
| PCT/CN2016/088186 WO2017206260A1 (en) | 2016-06-03 | 2016-07-01 | Polystyrene sulfonic acid resin catalyst, preparation method therefor and use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MY189165A true MY189165A (en) | 2022-01-30 |
Family
ID=60479515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MYPI2018701378A MY189165A (en) | 2016-06-03 | 2016-07-01 | Polystyrene sulfonic acid resin catalyst, preparation method therefor and use thereof |
Country Status (6)
| Country | Link |
|---|---|
| JP (1) | JP6526921B2 (en) |
| KR (1) | KR102047352B1 (en) |
| CN (1) | CN107457001B (en) |
| MY (1) | MY189165A (en) |
| SG (1) | SG11201803238YA (en) |
| WO (1) | WO2017206260A1 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112745184B (en) * | 2019-10-31 | 2022-08-12 | 中国石油化工股份有限公司 | Method for producing isooctene by overlapping mixed C4 raw material with high olefin content |
| CN113880702B (en) * | 2021-11-11 | 2024-02-02 | 万华化学集团股份有限公司 | A kind of preparation technology of isomeric tridecanol |
| CN114349588B (en) * | 2021-12-29 | 2023-09-19 | 万华化学集团股份有限公司 | A kind of preparation method of isooctane, isomeric dodecane and isomeric hexadecane |
| CN115772063B (en) * | 2022-12-07 | 2025-04-29 | 中国科学院大连化学物理研究所 | A preparation process and method of chloro(bromo)styrene |
| CN118875006B (en) * | 2024-07-15 | 2026-04-24 | 卫星化学股份有限公司 | A method for harmlessly inactivating ethylene oligomerization catalysts |
| CN121294022B (en) * | 2025-12-11 | 2026-02-24 | 山东海科化工有限公司 | Process for preparing biological aviation kerosene from waste grease |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3760026A (en) * | 1971-08-30 | 1973-09-18 | Phillips Petroleum Co | Synthesis of di-tert-butylethylene using olefin disproportionation |
| US4925989A (en) * | 1987-06-01 | 1990-05-15 | Texaco Inc. | MTBE preparation from isobutylene/TBA and methanol in presence of an acid resin catalyst |
| EP0800538B1 (en) * | 1994-12-30 | 2001-05-09 | Eastman Chemical Company | Process for preparing cellulose esters using a sulfonic acid resin catalyst |
| EP1388528B1 (en) * | 2002-08-06 | 2015-04-08 | Evonik Degussa GmbH | Process for the oligomerisation of isobutene contained in hydrocarbon streams containing n-butene |
| CN101440013B (en) * | 2007-11-22 | 2012-05-09 | 中国石油化工股份有限公司 | A kind of superposition reaction method of light olefin |
| US8067655B2 (en) * | 2008-05-29 | 2011-11-29 | Lyondell Chemical Technology, L.P. | Diisobutylene process |
| CN102020526B (en) * | 2009-09-09 | 2013-04-24 | 中国石油天然气股份有限公司 | A kind of method adopting tert-butanol to prepare isobutylene |
| CN101757946B (en) * | 2010-01-08 | 2012-07-18 | 凯瑞化工股份有限公司 | Multi-functional group resin catalyst and preparation method thereof |
| CN102319586B (en) * | 2011-06-10 | 2012-10-17 | 凯瑞化工股份有限公司 | Resin catalyst used in alkylation reaction of isobutene and butylene and preparation method thereof |
| CN102329182A (en) * | 2011-08-01 | 2012-01-25 | 天津市泰源工业气体有限公司 | Method for preparing isobutene through direct hydration method |
| BR112014014291A2 (en) * | 2011-12-28 | 2017-06-13 | Dow Global Technologies Llc | process for preparing a catalyst |
| JP2016085861A (en) * | 2014-10-27 | 2016-05-19 | 昭和電工株式会社 | Fuel battery electrode catalyst and method for manufacturing the same |
| CN104607252B (en) * | 2014-12-17 | 2016-09-14 | 烟台大学 | A kind of supported polystyrene sulfonic acid resin catalyst and preparation method thereof |
| CN105175203A (en) * | 2015-09-08 | 2015-12-23 | 山东成泰化工有限公司 | Method for preparing isobutene by MTBE (Methyl Tertiary Butyl Ether) |
| CN105130741B (en) * | 2015-10-13 | 2017-01-04 | 宁波金海晨光化学股份有限公司 | A kind of reactive distillation prepares the method for isoprene |
-
2016
- 2016-06-03 CN CN201610393945.3A patent/CN107457001B/en active Active
- 2016-07-01 JP JP2018540196A patent/JP6526921B2/en active Active
- 2016-07-01 MY MYPI2018701378A patent/MY189165A/en unknown
- 2016-07-01 WO PCT/CN2016/088186 patent/WO2017206260A1/en not_active Ceased
- 2016-07-01 KR KR1020187011882A patent/KR102047352B1/en active Active
- 2016-07-01 SG SG11201803238YA patent/SG11201803238YA/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN107457001B (en) | 2019-09-20 |
| JP6526921B2 (en) | 2019-06-05 |
| JP2018532591A (en) | 2018-11-08 |
| CN107457001A (en) | 2017-12-12 |
| SG11201803238YA (en) | 2018-05-30 |
| WO2017206260A1 (en) | 2017-12-07 |
| KR102047352B1 (en) | 2019-11-21 |
| KR20180059527A (en) | 2018-06-04 |
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