SU105655A1 - The method of obtaining a, a, a, W-tetrachloroalkanes - Google Patents
The method of obtaining a, a, a, W-tetrachloroalkanesInfo
- Publication number
- SU105655A1 SU105655A1 SU454416A SU454416A SU105655A1 SU 105655 A1 SU105655 A1 SU 105655A1 SU 454416 A SU454416 A SU 454416A SU 454416 A SU454416 A SU 454416A SU 105655 A1 SU105655 A1 SU 105655A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tetrachloroalkanes
- obtaining
- ethylene
- carbon tetrachloride
- reaction
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Известна реакци теломеризацин, позвол юща получать самые разнообразные органические соединени , однако она не получила промышленного осуществлени в св зи с р дом технологических трудностей.The known reaction of telomerizacin, which makes it possible to obtain a wide variety of organic compounds, however, it has not been commercialized due to a number of technological difficulties.
Предметом изобретени вл етс оригинальный способ проведени реакции теломеризации этилена с четыреххлористым углеродом, пригодный дл реализации в промышле)ности . С целью устранени возможности взрывов, процесс провод т в непрерывно действующем трубчатом реакторе, который через сборник продукта сообщаетс с атмосферой или с газгольдером через дроссельный вентиль и сборник.The subject of the invention is an original method of carrying out the reaction of telomerization of ethylene with carbon tetrachloride, suitable for implementation in the industry. In order to eliminate the possibility of explosions, the process is carried out in a continuously operating tubular reactor, which is in communication with the atmosphere through a product collector or with a gasholder through a throttle valve and a collection vessel.
В качестве инициатора теломерлзации примен етс азодинитрил диизомасл ной кислоть или перекись бензоила, что позвол ет снизить температуру реакции до 75-80° или облучениз ультрафиолетовым светом , дающее возможность вести процесс при температуре 30-40°.Azodinitrile diisobutyric acid or benzoyl peroxide is used as the telomerlization initiator, which allows the reaction temperature to be reduced to 75-80 ° or irradiated with ultraviolet light, making it possible to conduct the process at a temperature of 30-40 °.
Пример 1. Взаимодействие этилена и четырех.хлористого углерода в змеевиковом трубчатом реакторе проточного типа.Example 1. The interaction of ethylene and carbon tetrachloride in the coiled tubular flow type reactor.
В нижнюю часть обогреваемого змеевикового трубчатого реакто К1, изготовленного из нержавеющей стали ЭЯ1Т, с внутренним диаметром 14 мм и толщиной стенок 2 мм подают с помощью насоса раствор перекиси бензоила или азодинитрилт.иизомасл ной кислоты в четыреххлористом углероде. Одновременно в jieaKTop подаетс сжатый этилен.To the bottom of the heated coil tubular reactor K1, made of stainless steel EYa1T, with an inner diameter of 14 mm and a wall thickness of 2 mm, a solution of benzoyl peroxide or azodinitrite and isobutyric acid in carbon tetrachloride is pumped. At the same time, compressed ethylene is fed into the jieaKTop.
При реакции взаимодействи этилена и четыреххлористого углерода в присутствии перекиси бензои.ча (концентраци в ССЦ - 0,5%, температура в бане реактора 110° и давление в реакторе 200 атм) получают смесь, содержащую около 64% непрореагировавшего СС. около 4% тетрахлорпропановой фракции, около 13% тетрахлорпентановой фракции , около 12% тетрахлоргептановой фракции и около 7% остатка.In the reaction between ethylene and carbon tetrachloride in the presence of benzoic peroxide (concentration in the SST is 0.5%, the temperature in the bath of the reactor is 110 ° and the pressure in the reactor is 200 atm) a mixture containing about 64% of unreacted SS is obtained. about 4% tetrachloropropane fraction, about 13% tetrachloropentane fraction, about 12% tetrachloroheptane fraction, and about 7% of the residue.
При реакции этилена и четыреххлористого углерода в присутствии азодш-пггрила диизомасл ной кислоты (концентраци в CCli 0,6%. температура в бане 80-85° и давление 180 атм получают смесь, содержащую около 48% непрореагировавшего ecu, около 22% тетрахлорпентаBy the reaction of ethylene and carbon tetrachloride in the presence of azodi-pggryl diisobutyric acid (CCli concentration 0.6%. The temperature in the bath is 80-85 ° and the pressure 180 atm. A mixture is obtained containing about 48% unreacted ecu
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU454416A SU105655A1 (en) | 1953-04-29 | 1953-04-29 | The method of obtaining a, a, a, W-tetrachloroalkanes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU454416A SU105655A1 (en) | 1953-04-29 | 1953-04-29 | The method of obtaining a, a, a, W-tetrachloroalkanes |
Publications (1)
Publication Number | Publication Date |
---|---|
SU105655A1 true SU105655A1 (en) | 1956-11-30 |
Family
ID=48379037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU454416A SU105655A1 (en) | 1953-04-29 | 1953-04-29 | The method of obtaining a, a, a, W-tetrachloroalkanes |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU105655A1 (en) |
-
1953
- 1953-04-29 SU SU454416A patent/SU105655A1/en active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2404374A (en) | Polyfluorinated cycloparaffins and process for producing them | |
US2732338A (en) | Oxidation of organic compounds | |
GB857086A (en) | Process for the manufacture of carbon tetrachloride | |
US2398481A (en) | Process for catalyzed abnormal addition reactions | |
GB988006A (en) | Improvements in and relating to the production of oxygen-containing-organic compounds | |
SU105655A1 (en) | The method of obtaining a, a, a, W-tetrachloroalkanes | |
US2411983A (en) | Process for catalyzed abnormal addition reactions | |
GB902682A (en) | Process for the manufacture of fluorethylenes | |
Leifer et al. | Kinetics of gaseous reactions by means of the mass spectrometer. The thermal decomposition of dimethyl ether and acetaldehyde | |
GB581431A (en) | Improvements in or relating to the production of chlorinated derivatives of ethyl alcohol | |
US2481241A (en) | Method for removing chlorine from mixtures containing chlorine dioxide and chlorine | |
US3228865A (en) | Process for polymerizing tetrafluoroethylene | |
US2811485A (en) | Process for chlorinating dimethyl ether | |
Ruff et al. | Oxidations with oxygen difluoride. III | |
US3169104A (en) | Production of polyhaloalkyl sulfenyl chlorides | |
US2473161A (en) | Propane chlorination | |
US2873239A (en) | Process for making 2-mercaptoethyl ethers of diols | |
US1974747A (en) | Manufacture of arsenic acid | |
GB613519A (en) | Process of manufacture of hexachloride and products obtained by this process | |
US2461142A (en) | Production of beta-trichlorethane | |
DE705932C (en) | Process for the production of butadiene | |
US2503253A (en) | Azo catalysts in preparation of sulfonyl chlorides | |
US2906681A (en) | Process for the manufacture of carbon tetrachloride | |
Sosnovsky | Preparation of Trichloromethanesulfonyl Chloride. | |
US2744145A (en) | Production of benzene hexachloride in iron reaction chambers |