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-propanol

Info

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
Application number
DE19782853848
Other languages
German (de)
Inventor
Rudolf Knabl
Wilhelm Dipl Chem Dr Mack
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.)
Wacker Chemie AG
Original Assignee
Wacker Chemie 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 Wacker Chemie AG filed Critical Wacker Chemie AG
Priority to DE19782853848 priority Critical patent/DE2853848A1/en
Priority to US05/019,388 priority patent/US4220607A/en
Priority to EP79100807A priority patent/EP0004355B1/en
Priority to DE7979100807T priority patent/DE2960012D1/en
Publication of DE2853848A1 publication Critical patent/DE2853848A1/en
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/38Separation; Purification; Stabilisation; Use of additives
    • C07C17/42Use of additives, e.g. for stabilisation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Stabilised C2Cl4 contains, by wt. 0.001-0.01 (pref. 0.004-0.008) % of >=1 N- 1-5C-alkyl-morpholine, (I), opt. ring-substd. by 4 C-alkyl; 0.001-0.01 (pref. 0.004-0.008)% of >=1 alkylphenol, (II), contg. 1-18C alkyl in o- and/or p-position; 0.0005-0.002 (pref. 0.0008-0.0015) % diisopropylamine, (III), and 0.05-0.5 (pref. 0.1-0.3) % cyclohexene oxide (IV). C2Cl4 is stabilised against oxidative decomposition in contact with metals, alloys, metal salts, cutting oils, UV, light and heat. Acid absorption capacity is increased. The components act synergetically. The addn. of (IV) increases stabilising activity and prevents corrosion of Fe, Cu, Zn and Al.

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)

Patent p a n s p r u ch 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 desaen Gemische1 0,001 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 gemäß Patentanmeldung P 28 11 779.5 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.Patent p a n s p r u ch Containing stabilized perchlorethylene 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 thereof1 0.001 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 mixtures thereof, 0.0005 to 0.002% by weight of diisopropylamine and 0.005 to 0.5% by weight Cyclohexene oxide according to patent application P 28 11 779.5 d a d u r c h g e k e n n z e i c h n e t that it additionally contains 0.005 to 0.1% by weight of epoxypropanol.
DE19782853848 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 Ceased DE2853848A1 (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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