DE894910C - Process for the production of conversion products of trifluoroethene - Google Patents

Process for the production of conversion products of trifluoroethene

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Publication number
DE894910C
DE894910C DEF2536A DEF0002536A DE894910C DE 894910 C DE894910 C DE 894910C DE F2536 A DEF2536 A DE F2536A DE F0002536 A DEF0002536 A DE F0002536A DE 894910 C DE894910 C DE 894910C
Authority
DE
Germany
Prior art keywords
trifluoroethene
conversion products
production
hours
irradiation
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.)
Expired
Application number
DEF2536A
Other languages
German (de)
Inventor
Paul V Dr Fragstein
Wilhelm Dr Moschel
Wilhelm Dr Mueller
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Priority to DEF2536A priority Critical patent/DE894910C/en
Application granted granted Critical
Publication of DE894910C publication Critical patent/DE894910C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F14/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
    • C08F14/18Monomers containing fluorine
    • C08F14/185Monomers containing fluorine not covered by the groups C08F14/20 - C08F14/28

Description

Verfahren zur Herstellung von Umwandlungsprodukten des Trifluoräthens Halogenierte Vinylverbindungen, auch Trifluoräthen, lassen,sich in Emulsionen unter Zugabe eines Peroxyds als Aktivator polymerisieren.Process for the preparation of conversion products of trifluoroethene Halogenated vinyl compounds, including trifluoroethene, can be found in emulsions Polymerize by adding a peroxide as an activator.

Organische Verbindungen, die neben Fluor ein oder mehrere Halogenatome oder andere Substituenten außer Wasserstoff enthalten, hat man durch Einwirkung von Licht, insbesondere der Wellenlängen von :22oo bis 6ooo' A, polymerisiert. Bei diesen Verbindungen ist vorzugsweise die Doppelbindung dadurch aktiviert, daß eines der bei-den Kohlenstoff atome durch verschiedene Halogenatome oder andere Substituenten außer Wasserstoff gegenüber -den anderen besonders beschwert oder asymmetrisch ist.Organic compounds which in addition to fluorine contain one or more halogen atoms or other substituents other than hydrogen, one has by the action of light, in particular the wavelengths of: 22oo polymerized to 6ooo 'A. In these compounds, the double bond is preferably activated in that one of the two carbon atoms is particularly weighted or asymmetrical compared to the others due to various halogen atoms or other substituents besides hydrogen.

Gegenstand der Erfindung ist ein Verfahren zur Herstellung von Umwandlungsprodukten des Trifl-uoräthens (F, C = C 11 F), das darin besteht, daß man Trifltioräthen,d#---r Einwirkung von Licht, voT-zugsweise der Wellenlängen von :2t2oo bis 6ooo' A unterwirft. Das Trifluoräthen polymerisiert überraschenderweise bei Bestrahlung sehr schnell und vollständig, wobei die Eigenschaften des Polymerisates je nach der Bestrahlungsdauer variieren. Bei kurzzeitiger Bestrahlung, etwa 1/2 bis 5 Stunden, erhält man feste, aber plastische, leicht verformbare Massen. Bei länger dauernder Bestrahlung bis zu 40 Stunden gehen diese Massen allmählich in einen kristallinen, aber unter Druck verformbaren Zustand über.The invention relates to a process for the preparation of conversion products of trifluorethylene (F, C = C 11 F), which consists in that triflietene, the action of light, preferably of wavelengths from: 2t2oo to 6ooo 'A subjects. Surprisingly, the trifluoroethene polymerizes very quickly and completely on irradiation, the properties of the polymer varying depending on the duration of the irradiation. Short-term irradiation, about 1/2 to 5 hours, gives solid, but plastic, easily deformable materials. With longer exposure of up to 40 hours, these masses gradually change into a crystalline, but deformable state under pressure.

Belichtet man in Emulsion unter Zugabe eines Peroxydes als Aktivator, so erfolgt ebenfalls Polymerisation. Die weißen undurchsichtigen Polyrilerisate sind gut verformbar, bei erhöhlter Temperatur werden sie glasartig,durchscheinend, oberhalb 276' schmelzen sie, bis 300' ist keine Zersetzung zu beobachten. In,den gebräuchlichen organischen Lösungsmitteln sind sie unlöslich ' von Mineralsäuren werden sie unter den in der Technik üblichen Bedingungen nicht angegriffen. Sie stellen wertvolle Ausgangsprodukte für die Herstellung von Kunststoffen dar. Beispiel i Verflüssigtes Trifluoräthen wird der Sonnenbestrahlung oder der Bestrahlung durch eine UV-Lichtquelle ausgesetzt. Bereits nach wenigen Minuten beginnt die Polymerisation. je nach der Art der Bestrahlungsquelle ist sie nach i bis 4o Stunden beendet.If it is exposed in emulsion with the addition of a peroxide as an activator, polymerization also takes place. The white, opaque polyacrylates are easily deformable; at elevated temperatures they become glass-like, translucent, above 276 'they melt, up to 300' no decomposition can be observed. In "the common organic solvents they are insoluble " they are not attacked by mineral acids under the conditions customary in technology. They represent valuable starting products for the production of plastics. Example i Liquefied trifluoroethene is exposed to solar radiation or to radiation from a UV light source. Polymerization begins after just a few minutes. Depending on the type of irradiation source, it is over after 1 to 40 hours.

B e i s p ie l# 2, Nach Beispiel i wird verflüssigtes Trifluoräthen 6 Stunden lang dem Licht einer UV-Lampe ausgesetzt. Die Polymerisation ist dann vollständig. Man erhält ein festes, aber plastisches Polymerisat, das gut verformbar ist.B ice p y l # 2 of Example I liquefied Trifluoräthen is exposed for 6 hours to light from a UV lamp. The polymerization is then complete. A solid but plastic polymer is obtained which is easily deformable.

Bestrahlt man statt 6 Stunden etwa 4o Stunden, so ist das Polymerisat Kristallin, aber unter Druck noch verformbar. Im ersten Falle erfolgt der Umschlag in die glasartige Modifikation bei 148 bis 153', im zweiten Falle bei 170'.If irradiation is carried out for about 40 hours instead of 6 hours, the polymer is crystalline, but can still be deformed under pressure. In the first case the change to the glass-like modification takes place at 148 to 153 ', in the second case at 170'.

Claims (2)

PATENTANSPRÜCHE: i. Verfahren zur Herstellung von Urnwandlungsprodukten des Trifluoräthens, dadurch gekennzeichnet, daß man Trifluoräthen der Einwirkung von Licht, vorzugsweise der Wellenlängen von 2:2oo bis 6ooo.' A unterwirft. PATENT CLAIMS: i. Process for the preparation of conversion products of trifluoroethene, characterized in that trifluoroethene is subjected to the action of light, preferably of wavelengths from 2: 2oo to 6,000. ' A submits. 2. Verfahren nach Anspruch i, da-durch ge-.kennzeichnet, in Gegenwart daß eines man A-Ictivators Trifluoräthen der in Belichtung Emulsion unterwirft. Angezogene Druckschriften: USA.-Patentschrift Nr. 2 456.255.2. The method according to claim i, as-characterized by ge., In the presence of that one A-Ictivators trifluoroethene is subjected to the emulsion in exposure. Dressed References: U.S. Patent No. 2,456,255.
DEF2536A 1950-08-26 1950-08-27 Process for the production of conversion products of trifluoroethene Expired DE894910C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF2536A DE894910C (en) 1950-08-26 1950-08-27 Process for the production of conversion products of trifluoroethene

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE698215X 1950-08-26
DEF2536A DE894910C (en) 1950-08-26 1950-08-27 Process for the production of conversion products of trifluoroethene

Publications (1)

Publication Number Publication Date
DE894910C true DE894910C (en) 1953-10-29

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DEF2536A Expired DE894910C (en) 1950-08-26 1950-08-27 Process for the production of conversion products of trifluoroethene

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1145796B (en) * 1957-11-08 1963-03-21 Minnesota Mining & Mfg Process for the preparation of dispersions of polymers or copolymers of at least three fluorine atoms and, optionally, also of an ethylene containing a chlorine atom

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2456255A (en) * 1944-09-19 1948-12-14 Du Pont Polymers of trifluoroethylene and process for obtaining them

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2456255A (en) * 1944-09-19 1948-12-14 Du Pont Polymers of trifluoroethylene and process for obtaining them

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1145796B (en) * 1957-11-08 1963-03-21 Minnesota Mining & Mfg Process for the preparation of dispersions of polymers or copolymers of at least three fluorine atoms and, optionally, also of an ethylene containing a chlorine atom

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