DE2853848A1 - Stabilising tetra:chloroethylene to prevent contact metal corrosion - by adding alkyl-morpholine, alkylphenol, di:isopropylamine, cyclohexene oxide and opt. epoxy-propanol - Google Patents
Stabilising tetra:chloroethylene to prevent contact metal corrosion - by adding alkyl-morpholine, alkylphenol, di:isopropylamine, cyclohexene oxide and opt. epoxy-propanolInfo
- Publication number
- DE2853848A1 DE2853848A1 DE19782853848 DE2853848A DE2853848A1 DE 2853848 A1 DE2853848 A1 DE 2853848A1 DE 19782853848 DE19782853848 DE 19782853848 DE 2853848 A DE2853848 A DE 2853848A DE 2853848 A1 DE2853848 A1 DE 2853848A1
- Authority
- DE
- Germany
- Prior art keywords
- cyclohexene oxide
- alkylphenol
- opt
- morpholine
- stabilising
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/42—Use of additives, e.g. for stabilisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Zusatzanieldung zuAdditional application to
P 28 11 779.5 Stabilisiertes Perchloräthylen Perchloräthylen wird gemäß der deutschen Patentanmeldung P 28 11 779.5 mit einer Mischung aus Alkylphenolen, Aminen und Cyclohexenoxid stabilisiert. Es hat sich gezeigt, daß Cyclohexenoxid selbst in manchen Fällen ungenügende Stabilität zeigt.P 28 11 779.5 Stabilized Perchlorethylene Perchlorethylene is according to the German patent application P 28 11 779.5 with a mixture of alkylphenols, Amines and cyclohexene oxide stabilized. It has been shown that cyclohexene oxide shows insufficient stability even in some cases.
Gegenstand der Erfindung ist stabilisiertes Perchloräthylen enthaltend 0,001 bis 0,01 Gew.% N-Alkylmorpholin mit geraden oder verzweigten Alkylketten mit -1 bis 5 Kohlenstoffatomen und ggf. Alkylsubstituenten mit bis zu 4 Kohlenstoffatomen am Ring sowie dessen Gemische, 0s001 bis 0,01 Gew.% Alkylphenole mit gerader oder verzweigter Alkylkette mit 1 bis 18 Kohlenstoffatomen in o- und/oder p-Stellung sowie deren Gemische, 0,0005 bis 0,002 Gew.% Diisopropylamin und 0,005 bis 0,5 Gew.% Cyclohexenoxid d a d u r c h g e k e n n z e i c h n e t , daß es zusätzlich 0,005 bis 0,1 Gew.% Epoxipropanol enthält.The invention relates to stabilized perchlorethylene containing 0.001 to 0.01% by weight of N-alkylmorpholine with straight or branched alkyl chains with -1 to 5 carbon atoms and optionally alkyl substituents with up to 4 carbon atoms on the ring and mixtures thereof, 0.11 to 0.01% by weight of alkylphenols with straight or branched alkyl chain with 1 to 18 carbon atoms in o- and / or p-position and their mixtures, 0.0005 to 0.002 wt.% Diisopropylamine and 0.005 up to 0.5% by weight of cyclohexene oxide, it is indicated that it is additionally contains 0.005 to 0.1% by weight of epoxypropanol.
Ein Zusatz von Epoxipropanol kann überraschenderweise auch in Gegenwart von Verunreinigungen die stabilisierende Wirkung des Cyclohexenoxids erhalten. Es genügt bereits ein Zusatz an Epoxipropanol, der ein Zehntel oder weniger des Gewichtes des zugesetzten Cyclohexenoxids ausmacht.Surprisingly, epoxypropanol can also be added in the presence the stabilizing effect of cyclohexene oxide can be obtained from impurities. It All that is needed is an addition of epoxy propanol that is a tenth or less of the weight of the added cyclohexene oxide.
Beispiel l Zusatz von Epoxipropanol: Perchloräthylen wurde mit 50 ppm N-Methylmorpholin, 15 ppm Diisopropylamin, 50 ppm p.-tert.-Butylphenol, 2500 ppm Cyclohexenoxid und 200 ppm Epoxipropanol stabilisiert. Dann wurden in einem ersten Versuch 200 ppm und in einem zweiten Versuch 400 ppm Zinkchlorid zugefügt und anschließend 72 Stunden zum Sieden erhitzt. Nach dieser Zeit war das Cyclohexenoxid unterändert vorhanden. Im Gaschromatogramm wurden 2460 ppm Cyclohexenoxid wiedergefunden, Cyclopentylaldehyd war auch nicht in Spuren nachweisbar, das Gemisch zeigte keinen Fremdgeruch.Example l Addition of Epoxipropanol: Perchlorethylene was with 50 ppm N-methylmorpholine, 15 ppm diisopropylamine, 50 ppm p.-tert-butylphenol, 2500 ppm cyclohexene oxide and 200 ppm epoxypropanol stabilized. Then were in one first attempt 200 ppm and in a second attempt 400 ppm zinc chloride was added and then heated to the boil for 72 hours. After this time it was cyclohexene oxide under changed available. In the gas chromatogram, 2460 ppm cyclohexene oxide were found, Cyclopentylaldehyde was also not detectable in traces, the mixture showed none Foreign smell.
Claims (1)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19782853848 DE2853848A1 (en) | 1978-12-13 | 1978-12-13 | Stabilising tetra:chloroethylene to prevent contact metal corrosion - by adding alkyl-morpholine, alkylphenol, di:isopropylamine, cyclohexene oxide and opt. epoxy-propanol |
US05/019,388 US4220607A (en) | 1978-03-17 | 1979-03-12 | Stabilized perchloroethylene |
EP79100807A EP0004355B1 (en) | 1978-03-17 | 1979-03-16 | Stabilized perchloroethylene |
DE7979100807T DE2960012D1 (en) | 1978-03-17 | 1979-03-16 | Stabilized perchloroethylene |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19782853848 DE2853848A1 (en) | 1978-12-13 | 1978-12-13 | Stabilising tetra:chloroethylene to prevent contact metal corrosion - by adding alkyl-morpholine, alkylphenol, di:isopropylamine, cyclohexene oxide and opt. epoxy-propanol |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2853848A1 true DE2853848A1 (en) | 1980-07-03 |
Family
ID=6057074
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19782853848 Ceased DE2853848A1 (en) | 1978-03-17 | 1978-12-13 | Stabilising tetra:chloroethylene to prevent contact metal corrosion - by adding alkyl-morpholine, alkylphenol, di:isopropylamine, cyclohexene oxide and opt. epoxy-propanol |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE2853848A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0111894A1 (en) * | 1982-12-17 | 1984-06-27 | Wacker-Chemie GmbH | Process for stabilising epoxide-containing perchloroethylene |
EP0148481A2 (en) * | 1983-12-22 | 1985-07-17 | Wacker-Chemie GmbH | Process for the stabilisation of perchlorethylene containing cyclohexene oxide |
-
1978
- 1978-12-13 DE DE19782853848 patent/DE2853848A1/en not_active Ceased
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0111894A1 (en) * | 1982-12-17 | 1984-06-27 | Wacker-Chemie GmbH | Process for stabilising epoxide-containing perchloroethylene |
EP0148481A2 (en) * | 1983-12-22 | 1985-07-17 | Wacker-Chemie GmbH | Process for the stabilisation of perchlorethylene containing cyclohexene oxide |
EP0148481A3 (en) * | 1983-12-22 | 1985-10-09 | Wacker-Chemie Gmbh | Process for the stabilisation of perchlorethylene containing cyclohexene oxide |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8131 | Rejection |