GB581573A - Improved manufacture of vinyl halides - Google Patents

Improved manufacture of vinyl halides

Info

Publication number
GB581573A
GB581573A GB11293/43A GB1129343A GB581573A GB 581573 A GB581573 A GB 581573A GB 11293/43 A GB11293/43 A GB 11293/43A GB 1129343 A GB1129343 A GB 1129343A GB 581573 A GB581573 A GB 581573A
Authority
GB
United Kingdom
Prior art keywords
mercury
grams
catalyst
vinyl halides
support
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
GB11293/43A
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.)
Wingfoot Corp
Original Assignee
Wingfoot Corp
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 Wingfoot Corp filed Critical Wingfoot Corp
Publication of GB581573A publication Critical patent/GB581573A/en
Expired legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H02GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
    • H02KDYNAMO-ELECTRIC MACHINES
    • H02K49/00Dynamo-electric clutches; Dynamo-electric brakes
    • H02K49/10Dynamo-electric clutches; Dynamo-electric brakes of the permanent-magnet type
    • H02K49/104Magnetic couplings consisting of only two coaxial rotary elements, i.e. the driving element and the driven element
    • H02K49/106Magnetic couplings consisting of only two coaxial rotary elements, i.e. the driving element and the driven element with a radial air gap
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06Halogens; Compounds thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/07Preparation of halogenated hydrocarbons by addition of hydrogen halides
    • C07C17/08Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated hydrocarbons
    • HELECTRICITY
    • H02GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
    • H02KDYNAMO-ELECTRIC MACHINES
    • H02K49/00Dynamo-electric clutches; Dynamo-electric brakes
    • H02K49/10Dynamo-electric clutches; Dynamo-electric brakes of the permanent-magnet type
    • H02K49/104Magnetic couplings consisting of only two coaxial rotary elements, i.e. the driving element and the driven element

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

In the manufacture of vinyl halides by passing acetylene and hydrogen halide over mercury or a mercury halide, the catalyst is disposed on a continuous body of a non-volatile support so that any catalyst vaporised in the reaction zone is condensed in another part of the support. For example, the reaction tube may contain four grams of mercury or 15.4 grams of gas black, sandwiched between two 40 gram layers of gas black. The direction of flow of the reactants may be periodically reversed.ALSO:In the manufacture of vinyl halides by passing acetylene and hydrogen halide over mercury or a mercury halide, the catalyst is disposed on a continuous body of a non-volatile support so that any catalyst vaporised in the reaction zone will be condensed in another part of the support. For example, the reaction tube may contain 4 grams of mercury on 15.4 grams of gas black, sandwiched between two 40 gram layers of gas black. The direction of flow of the reactants may be periodically reversed.
GB11293/43A 1943-03-16 1943-07-12 Improved manufacture of vinyl halides Expired GB581573A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US581573XA 1943-03-16 1943-03-16
CH904189X 1943-06-02

Publications (1)

Publication Number Publication Date
GB581573A true GB581573A (en) 1946-10-17

Family

ID=25738792

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11293/43A Expired GB581573A (en) 1943-03-16 1943-07-12 Improved manufacture of vinyl halides

Country Status (2)

Country Link
CH (1) CH240244A (en)
GB (1) GB581573A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3268299A (en) * 1961-12-27 1966-08-23 Crawford & Russell Inc Apparatus for effecting chemical reactions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3268299A (en) * 1961-12-27 1966-08-23 Crawford & Russell Inc Apparatus for effecting chemical reactions

Also Published As

Publication number Publication date
CH240244A (en) 1945-12-15

Similar Documents

Publication Publication Date Title
GB1364658A (en) Nickel silica comosition with high nickel surface area
GB581573A (en) Improved manufacture of vinyl halides
ES473516A1 (en) Production of 1,1,1,2- tetrafluoroethane in vapour phase
ES306124A1 (en) Procedure of oxidation of a saturated aliciclic hydrocarbon. (Machine-translation by Google Translate, not legally binding)
Sneddon et al. Vapour synthesis of polylithium compounds: the effect of halogens in activating the carbon–hydrogen bond
GB573561A (en) Improvements in or relating to the manufacture of vinyl chloride
GB1108375A (en) Improvements in or relating to the manufacture of 2,6-dichloro-4-nitroaniline
GB963130A (en) Improvements in chromium base alloy
GB997363A (en) Improvements in or relating to methods of producing a b compounds
Banks et al. Perfluoro-2, 5-diazahexane-2, 5-dioxyl and its use in polymer chemistry and in polymer cross-linking
ES287853A1 (en) A procedure for the dehydration of hydrocarbons by reaction with iodine or bromo (Machine-translation by Google Translate, not legally binding)
ES318957A1 (en) Catalytic procedure for tricloroethylene manufacture. (Machine-translation by Google Translate, not legally binding)
GB1139516A (en) Manufacture of dichlorobutenes
GB967936A (en) Production of chlorinated hydrocarbons
GB740418A (en) Process for the manufacture of 1:2:3:4-tetrachloro-hexafluorobutane
FR1411095A (en) Direct manufacture of heavy gas by catalytic reforming under pressure of hydrocarbons
GB1081639A (en) Process for the manufacture of 2, 2-dichlorobutane
ES344937A1 (en) Process for the manufacture of carbon tetrachloride
DAMDINSURZN " MONGOLSKII ZPOS O GZSZR-KHANE"[Russian]
GB1054339A (en)
GB1094576A (en) Improvements in or relating to the production of aliphatic halogenohydrocarbons
GB733140A (en) Process for the catalytic hydrogenation of carbon monoxide
GB1170396A (en) Process for Hydrofluorination of Acetylenic Hydrocarbons
GB1129190A (en) Silver catalysts
GB934329A (en) Production of unsaturated hydrocarbon chlorides