BE561402A - - Google Patents
Info
- Publication number
- BE561402A BE561402A BE561402A BE561402A BE561402A BE 561402 A BE561402 A BE 561402A BE 561402 A BE561402 A BE 561402A BE 561402 A BE561402 A BE 561402A BE 561402 A BE561402 A BE 561402A
- Authority
- BE
- Belgium
- Prior art keywords
- zirconium
- compounds
- temperatures
- reaction
- weight
- Prior art date
Links
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 9
- 150000001348 alkyl chlorides Chemical class 0.000 claims description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 8
- 229910052726 zirconium Inorganic materials 0.000 claims description 8
- 239000007787 solid Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 6
- 229910007932 ZrCl4 Inorganic materials 0.000 claims description 5
- 238000001354 calcination Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 229910007928 ZrCl2 Inorganic materials 0.000 claims description 2
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 229910007926 ZrCl Inorganic materials 0.000 claims 1
- 229910007930 ZrCl3 Inorganic materials 0.000 claims 1
- 229920003169 water-soluble polymer Polymers 0.000 claims 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 17
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 12
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- 239000000460 chlorine Substances 0.000 description 9
- 150000003755 zirconium compounds Chemical class 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229940050176 methyl chloride Drugs 0.000 description 6
- 229910001928 zirconium oxide Inorganic materials 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- -1 aliphatic ethers Chemical class 0.000 description 4
- 150000002170 ethers Chemical class 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 229910006213 ZrOCl2 Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- IPCAPQRVQMIMAN-UHFFFAOYSA-L zirconyl chloride Chemical compound Cl[Zr](Cl)=O IPCAPQRVQMIMAN-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEG20679A DE1106964B (de) | 1956-10-05 | 1956-10-05 | Verfahren zur Herstellung von polymeren, Chlor- und Alkoxygruppen enthaltenden Zirkonverbindungen |
DEG22853A DE1112835B (de) | 1957-09-02 | 1957-09-02 | Verfahren zur Herstellung von polymeren, Chlor- und Alkoxygruppen enthaltenden Zirkonverbindungen |
Publications (1)
Publication Number | Publication Date |
---|---|
BE561402A true BE561402A (enrdf_load_stackoverflow) | 1957-10-31 |
Family
ID=61081977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE561402A BE561402A (enrdf_load_stackoverflow) | 1956-10-05 | 1957-10-04 |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE561402A (enrdf_load_stackoverflow) |
-
1957
- 1957-10-04 BE BE561402A patent/BE561402A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BE561402A (enrdf_load_stackoverflow) | ||
US2937201A (en) | Process for the production of azelaic acid | |
FR2489309A1 (fr) | Procede pour preparer des fluorures de difluorohalogenoacetyle a partir de polyfluoroethylene | |
FR2549039A1 (fr) | Procede de preparation de 3,3,3-trifluoro-2-trifluoro-mehylpropene | |
FR2467837A1 (fr) | Nouveaux composes acetyleniques, obtention et application en vue de la preparation de cetones alicycliques, telles que la b-damascenone | |
CA1280124C (fr) | Procede de preparation de 4-fluoroanilines a partir de 4-halogenonitrobenzenes | |
US2526859A (en) | Catalytic hydrogenation of betanaphthol to produce beta-tetralone | |
CA2224485A1 (fr) | Procede de preparation d'alpha, omega-bromochloroalcanes | |
JP3135660B2 (ja) | ペルフルオロ−オキシアジリジンの製造方法 | |
FR1464505A (fr) | Procédé pour la préparation du 1, 3-cyclohexadiényl-carbonitrile | |
JPS6126787B2 (enrdf_load_stackoverflow) | ||
SU1027161A1 (ru) | Способ получени 1-аллил-1-(3,7-диметилоктил)пиперидиний бромида | |
CH329044A (fr) | Procédé de préparation de 3,3-bis (chlorométhyl)-oxétane | |
CH272568A (fr) | Procédé de préparation de la cyclopentadécanone. | |
JPS5914473B2 (ja) | 1,1,3,3−テトラフルオロ−1,3−ジヒドロ−イソベンゾフランの製造方法 | |
FR2736634A1 (fr) | Procede de preparation d'alpha,omega-bromochloroalcanes | |
SU142644A1 (ru) | Способ получени эфиров аминооксиаланина | |
JPS5929680A (ja) | ロ−ズオキサイドの製造方法 | |
CH398565A (fr) | Procédé de préparation de l'acide cyclododécane-carboxylique | |
BE636259A (enrdf_load_stackoverflow) | ||
JPS5822450B2 (ja) | イソロンギホラン−3−オ−ル | |
BE624397A (enrdf_load_stackoverflow) | ||
CH349982A (fr) | Procédé de préparation d'un indole | |
JPH05229973A (ja) | 2,4−ジエチル−1,5−オクタンジオールの製法 | |
JPS5925347A (ja) | 1,1−ジアルコキシ−3−アルキン類の製法 |