BE549782A - - Google Patents
Info
- Publication number
- BE549782A BE549782A BE549782DA BE549782A BE 549782 A BE549782 A BE 549782A BE 549782D A BE549782D A BE 549782DA BE 549782 A BE549782 A BE 549782A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- ethylene
- compound
- metal
- sodium
- Prior art date
Links
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- 239000005977 Ethylene Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- -1 aryl compound Chemical class 0.000 claims 2
- 229920000573 polyethylene Polymers 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 239000004698 Polyethylene Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000003863 metallic catalyst Substances 0.000 claims 1
- 125000002524 organometallic group Chemical group 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 239000002244 precipitate Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 239000003054 catalyst Substances 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000012190 activator Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- CZHLPWNZCJEPJB-UHFFFAOYSA-N 1-chloro-3-methylbutane Chemical compound CC(C)CCCl CZHLPWNZCJEPJB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical group CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 1
- GWKIZYRKUYSSPX-UHFFFAOYSA-N dihydrido(dioxo)chromium Chemical compound [CrH2](=O)=O GWKIZYRKUYSSPX-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RO1154692X | 1956-03-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE549782A true BE549782A (de) |
Family
ID=20115411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE549782D BE549782A (de) | 1956-03-31 |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE549782A (de) |
| FR (1) | FR1154692A (de) |
-
0
- BE BE549782D patent/BE549782A/fr unknown
-
1956
- 1956-06-04 FR FR1154692D patent/FR1154692A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1154692A (fr) | 1958-04-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BE1008739A3 (fr) | Procede de preparation d'un polymere d'isobutylene. | |
| FR2715154A1 (fr) | Procédé de production d'oléfines alpha légères de pureté améliorée par oligomérisation, de l'éthylène. | |
| CN106588735A (zh) | 一种双(叔丁基过氧化异丙基)苯的生产方法 | |
| CN102336694B (zh) | 双(叔丁基过氧基)缩酮的合成方法 | |
| EP0668257A1 (de) | Katalysator sowie Verfahren zur Hydrierung von Benzol in dem dieser Katalysator angewendet wird | |
| Ruigh et al. | The preparation and properties of pure divinyl ether | |
| SA110310888B1 (ar) | عملية لإنتاج ثلاثي-بيوتيل فينول من تيار c4 مكرر مُصفّى | |
| US3057841A (en) | Polymerisation of ethylene with lithium borohydride and group ivb metal halides | |
| BE549782A (de) | ||
| CA2753453C (en) | Chemical process for the production of haloalkenone ethers | |
| US2394960A (en) | Process for polymerizing ethylene | |
| CN114044747A (zh) | 一种邻甲硫基苯甲腈的合成方法 | |
| EP0005394B1 (de) | Eine Magnesiumverbindung und ein Übergangsmetallhalogenid enthaltender Katalysator, Verfahren zur Herstellung dieses Katalysators, diesen Katalysator enthaltendes katalytisches System und dieses katalytische System verwendendes Polymerisationsverfahren | |
| US3277131A (en) | Preparation of pure alkoxytitanium iodides | |
| CA1106547A (fr) | Procede controle de polymerisation de l'ethylene | |
| US3257333A (en) | Conversion of methyl halides to high molecular weight organic compositions | |
| CN118791377B (zh) | 一种2,4,5-三氟苯乙酸的制备方法 | |
| BE552719A (de) | ||
| JP7516960B2 (ja) | 塩素化ポリマー及びその製造法 | |
| CH367329A (fr) | Procédé de polymérisation du butadiène | |
| CA2088132A1 (fr) | Procede de polymerisation de l'ethylene permettant d'obtenir un polymere de distribution large de masses moleculaires. procede de traitement de la composante catalytique | |
| TWEEDIE et al. | Hydrogenolysis by Metal Hydrides. II. Hydrogenolysis of Aryl Vinyl Ethers by Lithium Aluminum Hydride1 | |
| KR100379637B1 (ko) | 고순도, 고수율의 2-아미노-3,5-디브로모벤즈알데히드의제조방법 | |
| BE546600A (de) | ||
| BE579209A (de) |