NL8204661A - Werkwijze voor het bereiden van een alkyleencarbonaat. - Google Patents
Werkwijze voor het bereiden van een alkyleencarbonaat. Download PDFInfo
- Publication number
- NL8204661A NL8204661A NL8204661A NL8204661A NL8204661A NL 8204661 A NL8204661 A NL 8204661A NL 8204661 A NL8204661 A NL 8204661A NL 8204661 A NL8204661 A NL 8204661A NL 8204661 A NL8204661 A NL 8204661A
- Authority
- NL
- Netherlands
- Prior art keywords
- water
- alkylene
- process according
- carbon dioxide
- reaction
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 86
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 54
- -1 alkylene carbonate Chemical compound 0.000 claims description 45
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 42
- 239000001569 carbon dioxide Substances 0.000 claims description 35
- 238000006243 chemical reaction Methods 0.000 claims description 35
- 239000003054 catalyst Substances 0.000 claims description 34
- 125000002947 alkylene group Chemical group 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 31
- 150000002334 glycols Chemical class 0.000 claims description 23
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 16
- 230000015572 biosynthetic process Effects 0.000 claims description 16
- JNMIXMFEVJHFNY-UHFFFAOYSA-M methyl(triphenyl)phosphanium;iodide Chemical compound [I-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 JNMIXMFEVJHFNY-UHFFFAOYSA-M 0.000 claims description 10
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 15
- 235000011089 carbon dioxide Nutrition 0.000 description 9
- 230000036571 hydration Effects 0.000 description 9
- 238000006703 hydration reaction Methods 0.000 description 9
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 238000006460 hydrolysis reaction Methods 0.000 description 8
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 150000001649 bromium compounds Chemical class 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 150000004694 iodide salts Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 2
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical compound CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- JWOLLWQJKQOEOL-UHFFFAOYSA-N OOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOO JWOLLWQJKQOEOL-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000004714 phosphonium salts Chemical class 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- VFJYIHQDILEQNR-UHFFFAOYSA-M trimethylsulfanium;iodide Chemical compound [I-].C[S+](C)C VFJYIHQDILEQNR-UHFFFAOYSA-M 0.000 description 2
- 241000234282 Allium Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910017489 Cu I Inorganic materials 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- MMPOTNFPDMJTRR-UHFFFAOYSA-N OOOOOOOOOOO Chemical compound OOOOOOOOOOO MMPOTNFPDMJTRR-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000011162 ammonium carbonates Nutrition 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000003957 anion exchange resin Substances 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical group [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- UQFSVBXCNGCBBW-UHFFFAOYSA-M tetraethylammonium iodide Chemical compound [I-].CC[N+](CC)(CC)CC UQFSVBXCNGCBBW-UHFFFAOYSA-M 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- GOTIICCWNAPLMN-UHFFFAOYSA-M trimethylsulfanium;bromide Chemical compound [Br-].C[S+](C)C GOTIICCWNAPLMN-UHFFFAOYSA-M 0.000 description 1
- 150000003658 tungsten compounds Chemical class 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D321/00—Heterocyclic compounds containing rings having two oxygen atoms as the only ring hetero atoms, not provided for by groups C07D317/00 - C07D319/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32644781A | 1981-12-02 | 1981-12-02 | |
| US32644781 | 1981-12-02 | ||
| US06/441,191 US4786741A (en) | 1982-11-15 | 1982-11-15 | Preparation of alkylene carbonates |
| US44119182 | 1982-11-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8204661A true NL8204661A (nl) | 1983-07-01 |
Family
ID=26985411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8204661A NL8204661A (nl) | 1981-12-02 | 1982-12-01 | Werkwijze voor het bereiden van een alkyleencarbonaat. |
Country Status (18)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5138073A (en) * | 1981-12-02 | 1992-08-11 | Scientific Design Company, Inc. | Preparation of alkylene carbonates |
| US4400559A (en) * | 1982-06-14 | 1983-08-23 | The Halcon Sd Group, Inc. | Process for preparing ethylene glycol |
| US4851555A (en) * | 1984-10-25 | 1989-07-25 | Scientific Design Company, Inc. | Process for preparing alkylene oxides from alkylene carbonates |
| US4931571A (en) * | 1984-10-25 | 1990-06-05 | Scientific Design Company, Inc. | Process for preparing alkylene carbonates from alkylene oxides |
| DE4030283A1 (de) * | 1990-09-25 | 1992-03-26 | Ruetgerswerke Ag | Verfahren zur herstellung cyclischer carbonate |
| DE4105554A1 (de) | 1991-02-22 | 1992-08-27 | Bayer Ag | Verfahren zur herstellung von dialkylcarbonaten |
| JP3823149B2 (ja) * | 2002-03-06 | 2006-09-20 | 独立行政法人産業技術総合研究所 | アルキレンカーボネート合成触媒 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE740366C (de) * | 1939-03-11 | 1943-10-19 | Ig Farbenindustrie Ag | Verfahren zur Herstellung von Glykolcarbonat |
| US2773070A (en) * | 1952-10-31 | 1956-12-04 | Jefferson Chem Co Inc | Catalytic process for producing alkylene carbonates |
| US2994705A (en) * | 1958-12-08 | 1961-08-01 | Pure Oil Co | Preparation of cyclic alkylene carbonates in the presence of organic phosphonium compounds |
-
1982
- 1982-11-24 IN IN869/DEL/82A patent/IN159117B/en unknown
- 1982-11-24 AU AU90842/82A patent/AU558415B2/en not_active Ceased
- 1982-12-01 BR BR8206977A patent/BR8206977A/pt not_active IP Right Cessation
- 1982-12-01 KR KR8205390A patent/KR860001856B1/ko not_active Expired
- 1982-12-01 DE DE19823244456 patent/DE3244456A1/de active Granted
- 1982-12-01 NL NL8204661A patent/NL8204661A/nl not_active Application Discontinuation
- 1982-12-01 NO NO824030A patent/NO162519C/no unknown
- 1982-12-01 SU SU823522506A patent/SU1574175A3/ru active
- 1982-12-01 FR FR8220165A patent/FR2517306B1/fr not_active Expired
- 1982-12-01 SE SE8206848A patent/SE454088B/sv not_active IP Right Cessation
- 1982-12-02 ES ES517885A patent/ES8401435A1/es not_active Expired
- 1982-12-02 CH CH7020/82A patent/CH653984A5/fr not_active IP Right Cessation
- 1982-12-02 BG BG058786A patent/BG48693A3/xx unknown
- 1982-12-02 AR AR291484A patent/AR231432A1/es active
- 1982-12-02 IT IT49611/82A patent/IT1189430B/it active
- 1982-12-02 GB GB08234366A patent/GB2113207B/en not_active Expired
- 1982-12-02 RO RO82109206A patent/RO85557A/ro unknown
- 1982-12-02 MX MX195419A patent/MX163138B/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB2113207B (en) | 1986-05-08 |
| GB2113207A (en) | 1983-08-03 |
| DE3244456C2 (enrdf_load_stackoverflow) | 1990-07-05 |
| FR2517306A1 (fr) | 1983-06-03 |
| IN159117B (enrdf_load_stackoverflow) | 1987-03-28 |
| SE454088B (sv) | 1988-03-28 |
| AR231432A1 (es) | 1984-11-30 |
| CH653984A5 (fr) | 1986-01-31 |
| AU9084282A (en) | 1983-06-09 |
| AU558415B2 (en) | 1987-01-29 |
| KR860001856B1 (ko) | 1986-10-24 |
| NO162519C (no) | 1990-01-10 |
| KR840002762A (ko) | 1984-07-16 |
| ES517885A0 (es) | 1983-12-16 |
| NO824030L (no) | 1983-06-03 |
| SE8206848L (sv) | 1983-06-03 |
| SU1574175A3 (ru) | 1990-06-23 |
| IT1189430B (it) | 1988-02-04 |
| IT8249611A0 (it) | 1982-12-02 |
| FR2517306B1 (fr) | 1986-02-28 |
| SE8206848D0 (sv) | 1982-12-01 |
| RO85557A (ro) | 1985-03-15 |
| ES8401435A1 (es) | 1983-12-16 |
| BG48693A3 (en) | 1991-04-15 |
| NO162519B (no) | 1989-10-02 |
| MX163138B (es) | 1991-08-30 |
| DE3244456A1 (de) | 1983-06-23 |
| BR8206977A (pt) | 1983-10-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1140355B1 (en) | Catalytic oxidation of alkanes to corresponding acids | |
| US6143928A (en) | Catalysts for low temperature selective oxidation of propylene, methods of making and using the same | |
| US7642372B2 (en) | Process for preparing carboxylic acids and derivatives thereof | |
| CA1305179C (en) | Acetic acid from ethane, ethylene and oxygen | |
| CA1181098A (en) | Hydroxylation of olefins | |
| CA1248119A (en) | Preparation of alkylene carbonates | |
| CN105873890B (zh) | 用于制备纯化的羧酸的氧化方法 | |
| JPS6214535B2 (enrdf_load_stackoverflow) | ||
| NL8204661A (nl) | Werkwijze voor het bereiden van een alkyleencarbonaat. | |
| US4511548A (en) | Ammoxidation of methanol to produce hydrogen cyanide | |
| Behr et al. | The telomerisation of 1, 3-butadiene and carbon dioxide: process development and optimisation in a continuous miniplant | |
| NO133754B (enrdf_load_stackoverflow) | ||
| Clark et al. | Environmentally Friendly Chemistry Using Supported Reagent Catalysts: Chemically‐Modified Mesoporous Solid Catalysts | |
| JP2002537085A (ja) | エタンから酢酸への酸化用触媒 | |
| US6087297A (en) | Catalysts for gas phase production of acetic acid from ethane, processes of making the same and methods of using same | |
| CN106221786B (zh) | 一种石脑油的转化方法 | |
| US5639924A (en) | Process for the production of 1,1,1-trifluoroethane | |
| JPH11114418A (ja) | イソブタンの気相接触酸化反応用触媒およびこれを用いてなるアルケンおよび／または含酸素化合物の製造方法 | |
| JPH0148889B2 (enrdf_load_stackoverflow) | ||
| EP0127804B1 (en) | 4,4-dihalohexahydrophthalic anhydrides and 4-fluorotetrahydrophthalic anhydride, and processes for their preparation and utilization | |
| WO2007001649A2 (en) | Oxidation of alkanes | |
| EP0105591B1 (en) | Catalytic conversion of methanol into light olefins | |
| JP3517279B2 (ja) | 低級オレフィンの二量化法 | |
| CA1235422A (en) | Process for the preparation of 4-fluorophthalic anhydride | |
| JPH0149269B2 (enrdf_load_stackoverflow) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BA | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BC | A request for examination has been filed | ||
| DNT | Communications of changes of names of applicants whose applications have been laid open to public inspection |
Free format text: PROCESS RESEARCH AND DEVELOPMENT COMPANY |
|
| CNR | Transfer of rights (patent application after its laying open for public inspection) |
Free format text: SCIENTIFIC DESIGN COMPANY, INC. TE LITTLE FERRY |
|
| BV | The patent application has lapsed |