ES229953A1 - Improved process for the production of vinyl chloride from 1,2-dichlorethane and acetylene - Google Patents

Improved process for the production of vinyl chloride from 1,2-dichlorethane and acetylene

Info

Publication number
ES229953A1
ES229953A1 ES0229953A ES229953A ES229953A1 ES 229953 A1 ES229953 A1 ES 229953A1 ES 0229953 A ES0229953 A ES 0229953A ES 229953 A ES229953 A ES 229953A ES 229953 A1 ES229953 A1 ES 229953A1
Authority
ES
Spain
Prior art keywords
catalyst
dehydrochlorination
reactor
dichlorethane
zone
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
ES0229953A
Other languages
Spanish (es)
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.)
Societe Belge de lAzote et des Produits Chimiques du Marly SA
Original Assignee
Societe Belge de lAzote et des Produits Chimiques du Marly SA
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 Societe Belge de lAzote et des Produits Chimiques du Marly SA filed Critical Societe Belge de lAzote et des Produits Chimiques du Marly SA
Publication of ES229953A1 publication Critical patent/ES229953A1/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/25Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00002Chemical plants
    • B01J2219/00004Scale aspects
    • B01J2219/00006Large-scale industrial plants
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

Landscapes

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

Abstract

A dehydrochlorination catalyst consisting of an active carbon base impregnated with a metal salt (e.g. barium chloride) is regenerated by treatment with inert gases (e.g. nitrogen) containing water vapour and only traces of oxygen at elevated temperature (e.g. 900 DEG C.).ALSO:Vinyl chloride is produced partly by catalytic dehydrochlorination of 1 : 2-dichlorethane and partly by catalytic synthesis from the hydrochloric acid so produced and acetylene, by a process wherein the catalytic dehydrochlorination is effected in a first substantially upright reaction zone and the catalytic synthesis in a second such zone, the catalyst in each zone being in the form of a powder having a particle size of 40-200 microns in diameter, 95 per cent of the particles being of 50-150 microns diameter, and wherein the reactants and reaction products in each zone are in the gaseous state, the amount of catalyst and rate of flow of reactants and reaction products through each zone being such that the catalyst is maintained in fluidized suspension throughout substantially the entire length of each reaction zone, and that in each reaction zone the upper level of said suspension is adjacent to the upper limit of the reaction zone. Preferably the dehydrochlorination is effected at 350-450 DEG C. in the presence of a catalyst consisting of a base (e.g. silica gel, clay or active carbon) impregnated with a metal salt (e.g. barium chloride), which may be regenerated by continuously extracting it from the upper part of the reaction zone and recycling it to the lower part after burning off the tar deposited thereon or (in the case of a catalyst with an active carbon base) treating it with inert gases (e.g. nitrogen) containing water vapour and only traces of oxygen at elevated temperatures (e.g. 900 DEG C.). The synthesis step is preferably carried out at 120-160 DEG C. in the presence of powdered active carbon impregnated with mercuric chloride, using acetylene substantially free from catalyst poisons. A suitable apparatus, described with the aid of a drawing, comprises a double-column vertical dehydrochlorination reactor and a double-column vertical synthesis reactor, there being an injector at the foot of each reactor for supplying the fluidized catalyst suspensions thereto and a cyclone device at the top of each reactor and connected to the top of each lower column for receiving product gases therefrom, a dichlorethane distillation unit for receiving excess dichlorethane liquefied from the products leaving the dehydrochlorination reactor and for returning part of said excess dichlorethane to said reaction as a recycle food, a product distillation unit for separating the products leaving the synthesis reactor into recycle acetylene and dichlorethane and product vinyl chloride, and a regenerator for the dehydrochlorination catalyst. The latter preferably comprises cyclone means for collecting the powdered catalyst, conduit means for causing hot gases to suspend said catalyst during the regeneration and to deposit the regenerated catalyst in said cyclone means, further conduit means connecting said cyclone means to the supply mains for the dichlorethane feed to the dehydrochlorination reactor, and blower means in said supply mains to entrain the regenerated catalyst with the gases fed to the foot of said reactor. A jacket may surround at least part of the lower column of the dehydrochlorination reactor, there being conduit means for causing hot fluid to enter said jacket near the top and leave the bottom thereof. A numerical example describes the production of 5 tons a day of pure vinyl chloride.
ES0229953A 1955-08-05 1956-07-21 Improved process for the production of vinyl chloride from 1,2-dichlorethane and acetylene Expired ES229953A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB22637/55A GB801663A (en) 1955-08-05 1955-08-05 Improved process for the production of vinyl chloride from 1,2-dichlorethane and acetylene

Publications (1)

Publication Number Publication Date
ES229953A1 true ES229953A1 (en) 1956-10-16

Family

ID=10182663

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0229953A Expired ES229953A1 (en) 1955-08-05 1956-07-21 Improved process for the production of vinyl chloride from 1,2-dichlorethane and acetylene

Country Status (4)

Country Link
BE (1) BE549468A (en)
ES (1) ES229953A1 (en)
FR (1) FR1157791A (en)
GB (1) GB801663A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117943132A (en) * 2024-03-26 2024-04-30 浙江省白马湖实验室有限公司 In-situ regeneration method of carbon-based catalyst

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES325919A1 (en) * 1965-06-09 1967-03-01 The B F Goodrich Company Procedure for preparing 1,2-dichloroethane. (Machine-translation by Google Translate, not legally binding)
BE755150A (en) * 1969-08-22 1971-02-22 Dow Chemical Co USE OF HYDROBROMIDE ACID FROM THE PYROLYSIS OF ETHYLENE DUDIBROMIDE,
FR2639851B1 (en) * 1988-12-01 1991-10-18 Atochem METHOD FOR CLEANING TUBES IN OPERATION USING PARTICLES
GB201509019D0 (en) 2015-05-27 2015-07-08 Johnson Matthey Plc Process and catalyst
CN112844460B (en) * 2019-11-27 2022-06-03 中国科学院大连化学物理研究所 Catalyst for preparing chloroethylene by acetylene and dichloroethane coupling reaction and application thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117943132A (en) * 2024-03-26 2024-04-30 浙江省白马湖实验室有限公司 In-situ regeneration method of carbon-based catalyst

Also Published As

Publication number Publication date
BE549468A (en) 1900-01-01
FR1157791A (en) 1958-06-03
GB801663A (en) 1958-09-17

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