DE1154480B - Verfahren zur Durchfuehrung von kontinuierlichen Telomerisationen - Google Patents
Verfahren zur Durchfuehrung von kontinuierlichen TelomerisationenInfo
- Publication number
- DE1154480B DE1154480B DES64288A DES0064288A DE1154480B DE 1154480 B DE1154480 B DE 1154480B DE S64288 A DES64288 A DE S64288A DE S0064288 A DES0064288 A DE S0064288A DE 1154480 B DE1154480 B DE 1154480B
- Authority
- DE
- Germany
- Prior art keywords
- reaction
- telogen
- liquid
- temperature
- catalyst
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 42
- 239000007788 liquid Substances 0.000 claims description 34
- 230000003797 telogen phase Effects 0.000 claims description 26
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 25
- 239000003054 catalyst Substances 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 210000003411 telomere Anatomy 0.000 claims description 5
- 102000055501 telomere Human genes 0.000 claims description 5
- 108091035539 telomere Proteins 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- 238000004880 explosion Methods 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 2
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 claims description 2
- 239000000725 suspension Substances 0.000 claims description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 claims 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims 2
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims 2
- POJPQMDDRCILHJ-UHFFFAOYSA-N 1,1,1,2,2,2-hexabromoethane Chemical compound BrC(Br)(Br)C(Br)(Br)Br POJPQMDDRCILHJ-UHFFFAOYSA-N 0.000 claims 1
- ZABBFAHZPHMIJC-UHFFFAOYSA-N 1,1-Dibromopropan-2-one Chemical compound CC(=O)C(Br)Br ZABBFAHZPHMIJC-UHFFFAOYSA-N 0.000 claims 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- HLHNOIAOWQFNGW-UHFFFAOYSA-N 3-bromo-4-hydroxybenzonitrile Chemical compound OC1=CC=C(C#N)C=C1Br HLHNOIAOWQFNGW-UHFFFAOYSA-N 0.000 claims 1
- HGINADPHJQTSKN-UHFFFAOYSA-N Monoethyl malonic acid Chemical compound CCOC(=O)CC(O)=O HGINADPHJQTSKN-UHFFFAOYSA-N 0.000 claims 1
- 238000006480 benzoylation reaction Methods 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 claims 1
- 230000002349 favourable effect Effects 0.000 claims 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 229930195734 saturated hydrocarbon Natural products 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 description 4
- 239000004342 Benzoyl peroxide Substances 0.000 description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 1
- DRUIESSIVFYOMK-UHFFFAOYSA-N Trichloroacetonitrile Chemical compound ClC(Cl)(Cl)C#N DRUIESSIVFYOMK-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- -1 acyl peroxides Chemical class 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1211758 | 1958-08-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1154480B true DE1154480B (de) | 1963-09-19 |
Family
ID=11139464
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DES64288A Pending DE1154480B (de) | 1958-08-09 | 1959-08-04 | Verfahren zur Durchfuehrung von kontinuierlichen Telomerisationen |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE581001A (en, 2012) |
DE (1) | DE1154480B (en, 2012) |
FR (1) | FR1235723A (en, 2012) |
GB (1) | GB907148A (en, 2012) |
NL (1) | NL241574A (en, 2012) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1084724B (de) * | 1956-01-13 | 1960-07-07 | Degussa | Kontinuierliches Verfahren zur Durchfuehrung von Telomerisationen |
-
0
- NL NL241574D patent/NL241574A/xx unknown
- BE BE581001D patent/BE581001A/xx unknown
-
1959
- 1959-07-22 GB GB2521759A patent/GB907148A/en not_active Expired
- 1959-08-04 FR FR802011A patent/FR1235723A/fr not_active Expired
- 1959-08-04 DE DES64288A patent/DE1154480B/de active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1084724B (de) * | 1956-01-13 | 1960-07-07 | Degussa | Kontinuierliches Verfahren zur Durchfuehrung von Telomerisationen |
Also Published As
Publication number | Publication date |
---|---|
NL241574A (en, 2012) | |
FR1235723A (fr) | 1960-07-08 |
GB907148A (en) | 1962-10-03 |
BE581001A (en, 2012) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1032741B (de) | Verfahren zur Herstellung von Aluminiumalkylen | |
DE1155910B (de) | Verfahren zur Herstellung von Telomeren oder Addukten von Fluoralkenen oder Fluorpolyenen | |
DE2651637C2 (de) | Verfahren zur Herstellung von Oligomerengemischen aus α-Olefinen | |
DE1154480B (de) | Verfahren zur Durchfuehrung von kontinuierlichen Telomerisationen | |
DD158547A5 (de) | Verfahren zur herstellung von alkylsulfochloriden | |
DE3202292C2 (de) | Verfahren zur kontinuierlichen Bildung eines Säurefluorids | |
DE1792011C3 (de) | Verfahren zur katalytischen Umesterung von Glyceridölen | |
DE740408C (de) | Herstellung von aliphatischen Chlorkohlenwasserstoffen | |
DE1468787C3 (en, 2012) | ||
DE1520113B2 (de) | Verfahren zur polymerisation von aethylen | |
DE2434370A1 (de) | Verfahren zur herstellung von acrylamid | |
AT229019B (de) | Verfahren zur Polymerisation von Äthylen | |
DE69714907T2 (de) | Vorrichtung und Verfahren zur Produktion von 2-Hydroxycarbonsäureoligomeren | |
DE1468575A1 (de) | Kontinuierliches Verfahren zum Herstellen der Mononitroverbindungen von Benzol,Toluol oder Chlorbenzol | |
DE1962689C3 (de) | Wärmeübertragungsmittel auf der Basis von Äthyldiphenylen sowie Verfahren zur Herstellung von Gemischen aus 3- und 4Äthyldiphenylen | |
DE1595220C (de) | Verfahren zum Neutralisieren von v.er unreinigten Entasctmngsflussigkeiten, die bei der Entfernung von Katalysatorruckstan den aus alpha Olefinpolymeren anfallen | |
DE2331082B2 (de) | Verfahren zur kontinuierlichen oxydation von substituierten benzolen oder benzolderivaten mit salpetersaeure | |
DE1520113C (de) | Verfahren zur Polymerisation von Athylen | |
DE975166C (de) | Verfahren zur Erhoehung des Schmelzpunktes von Petrolatum | |
DE1258406C2 (de) | Verfahren zur herstellung von aluminiumtrialkylen | |
DE2156329C3 (de) | Verfahren zur Herstellung von Perchlormethylmercaptan | |
AT155811B (de) | Verfahren zur fortlaufenden Herstellung von gebrauchsfertigem Polyvinylchlorid. | |
DE896191C (de) | Verfahren zur Herstellung von Chlorkohlenwasserstoffen | |
DE1595220B2 (de) | Verfahren zum neutralisieren von verunreinigten entschungs fluessigkeiten die bei der entfernung von katalysator rueckstaenden aus alpha olefinp/ lymeren anfallen | |
DE947737C (de) | Verfahren zur Herstellung fluessiger, oelartiger und wachsartiger, Fluor enthaltender Polymerisate oder Mischpolymerisate |