CH256846A - Process for the preparation of a fluoroalkylene. - Google Patents
Process for the preparation of a fluoroalkylene.Info
- Publication number
- CH256846A CH256846A CH256846DA CH256846A CH 256846 A CH256846 A CH 256846A CH 256846D A CH256846D A CH 256846DA CH 256846 A CH256846 A CH 256846A
- Authority
- CH
- Switzerland
- Prior art keywords
- fluoroalkylene
- preparation
- starting material
- pyrolysis
- alloy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Fluoralkylens. Gegenstand der Erfindung ist ein Ver fahren zur Herstellung des an sich bekann ten Fluoralkylens der Formel CHz = CF_ durch Pyrolyse des Fluorchloralkyls der For mel<B>CH,</B> # C Cl F'2. Unter Pyrolyse wird die Umwandlung des Ausgangsstoffes durch die Einwirkung von Hitze verstanden.
Zweckmässig wird das Verfahren durch kontinuierliches Durchleiten des Ausgangs materials durch ein auf die pyrolytisch wirk same Temperatur erhitztes Rohr durchge führt. Dass Rohr besteht vorteilhaft aus einem Material, welches gegenüber der Re aktion und den Reaktionsprodukten inert ist. Besonders geeignet ist ein Nickelrohr, wel ches: auf der Innenseite mit einem Platin belag versehen ist und auf der Aussenseite einen Mantel aufweist, der aus einer Legie rung von etwa 80 % Ni, 14 % Cr und 6 % Fe besteht. Die bevorzugte Temperatur für die Pyrolyse liegt ungefähr bei 715 C.
Der durch das neue Verfahren her gestellte Stoff kann zur Herstellung von Polymeren und gopolymeren für Spezial filme verwendet werden.
Beispiel: CHg # C Cl F, wurde in einer Menge von 120 g pro Stunde durch ein Nickelrohr ge leitet, das einen innern Platinbelag und einen äussern Schutzmantel aus einer Legierung aus etwa 80 % Ni, 14 % - Cr und 6 % Fe. auf wies und dessen Länge 108 cm und dessen Innendurchmesser 13,7 mm betrug. Durch elektrische Heizung wurde über eine Länge von schätzungsweise 200 mm eine Temperatur von 715 C aufrechterhalten.
Die Reaktions produkte wurden mit Wasser gewaschen, ge trocknet und in zwei Vorlagen kondensiert. Die erste Vorlage wurde auf ungefähr - 70 C gekühlt, während die zweite Vor lage in einem aus flüssigem Stickstoff be stehenden Bad gekühlt wurde. Wie durch Säurebestimmung im .Waschwasser festge stellt wurde, betrug die Umwandlung unge fähr 50 % des Ausgangsmaterials.
Die Pyro lyse verlief glatt unter Bildung von prak tisch reinem<B>CH,</B> = CFZ mit einem Siede punkt von - 83,9 C und einer Dampfdichte von 2,58 g pro Liter bei 28 C und 756 mm Druck.
Process for the preparation of a fluoroalkylene. The invention relates to a process for the preparation of the known fluoroalkylene of the formula CHz = CF_ by pyrolysis of the fluorochloroalkyl of the formula <B> CH, </B> # C Cl F'2. Pyrolysis is the conversion of the starting material through the action of heat.
The process is advantageously carried out by continuously passing the starting material through a tube heated to the pyrolytically effective temperature. The tube is advantageously made of a material which is inert to the reaction and the reaction products. Particularly suitable is a nickel tube which is provided with a platinum coating on the inside and has a jacket on the outside which consists of an alloy of about 80% Ni, 14% Cr and 6% Fe. The preferred temperature for pyrolysis is around 715 C.
The fabric produced by the new process can be used to manufacture polymers and copolymers for special films.
Example: CHg # C Cl F, was passed through a nickel tube in an amount of 120 g per hour, which had an inner platinum coating and an outer protective jacket made of an alloy of about 80% Ni, 14% Cr and 6% Fe. and its length was 108 cm and its inner diameter was 13.7 mm. A temperature of 715 ° C was maintained by electrical heating over a length of approximately 200 mm.
The reaction products were washed with water, dried and condensed in two templates. The first template was cooled to about -70 C, while the second template was cooled in a bath consisting of liquid nitrogen. As was found by determining the acid in the washing water, the conversion was approximately 50% of the starting material.
The pyrolysis proceeded smoothly with the formation of practically pure <B> CH, </B> = CFZ with a boiling point of - 83.9 C and a vapor density of 2.58 g per liter at 28 C and 756 mm pressure.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US256846XA | 1942-03-17 | 1942-03-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH256846A true CH256846A (en) | 1948-09-15 |
Family
ID=21827485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH256846D CH256846A (en) | 1942-03-17 | 1945-10-27 | Process for the preparation of a fluoroalkylene. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH256846A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2783821A1 (en) * | 1998-09-03 | 2000-03-31 | Atochem Elf Sa | Process for the manufacture of vinylidine fluoride and 1,2-difluroethylene by the pyrolysis of 1-chloro-2,2-difluoroethane in a reactor of which the metallic walls function as a catalyst |
-
1945
- 1945-10-27 CH CH256846D patent/CH256846A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2783821A1 (en) * | 1998-09-03 | 2000-03-31 | Atochem Elf Sa | Process for the manufacture of vinylidine fluoride and 1,2-difluroethylene by the pyrolysis of 1-chloro-2,2-difluoroethane in a reactor of which the metallic walls function as a catalyst |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2226376A1 (en) | Tolane and process for their preparation | |
DE1593233A1 (en) | Process for the preparation of new fluorine-containing epoxy compounds | |
CH256846A (en) | Process for the preparation of a fluoroalkylene. | |
DE1771162B1 (en) | PROCESS FOR ELECTROLYTIC DEPOSITION OF DENSE AND FASTENING CHROME COATINGS ON ZIRCONIUM AND ZIRCONIUM ALLOYS | |
DE830050C (en) | Process for the preparation of 5-substituted furan-2-carboxylic acid esters | |
DE2205924A1 (en) | Drive means door Rankine prime movers | |
DE895233C (en) | Generation of thick chrome layers of great hardness | |
AT215036B (en) | Process for the production of a composite body or composite material | |
DE492510C (en) | Process for the production of indanone | |
CH501618A (en) | Substd phenethylalcohols analgesics anti-inflammatory | |
DE3345309A1 (en) | AQUEOUS QUARKING MEDIUM FOR LIGHT ALLOY | |
DE649607C (en) | Process for the preparation of compounds from selenium and carbon | |
AT224652B (en) | Process for the production of vinyl phosphonic acid | |
DE1771162C (en) | Process for the electrolytic deposition of dense and firmly adhering chrome coatings on zirconium and zirconium alloys | |
US1885292A (en) | Mothproofing composition | |
AT56495B (en) | Method of treating betulin. | |
AT229303B (en) | Process for the production of new basic esters of α-phenyl-α-isopropylglycolic acid or its acyl derivatives and their salts and quaternary ammonium compounds | |
AT160299B (en) | Process for the production of ether-alcohol mixtures suitable as fuel for internal combustion engines. | |
AT282601B (en) | Process for the preparation of new, mixed substituted 1-phenoxy-3-alkylaminopropanolen- (2) and their acid addition salts | |
DE878642C (en) | Process for the cyclization of geranylacetones to 2, 5, 5, 9-tetramethylhexahydrochromones or 3-oxytetrahydrojonones | |
DE650942C (en) | Process for the preparation of the sulfmethylaether of 2-methyl-7-sulfhydroxy- and 2-methyl-6-sulfhydroxy-ª ‰, ª ‰ -naphthothiazoles | |
DE887815C (en) | Process for the preparation of disubstituted carboxylic acid diamides | |
DE2236875C3 (en) | Process for the production of nuclear chlorinated phthalic anhydrides by catalytic air oxidation | |
CH295657A (en) | Process for the technical production of acetic acid from carbon monoxide and methanol. | |
DE934948C (en) | Process for the preparation of 1, 2, 4-trimethyl-3-phenyl-pyrazolone- (5) |