GB829760A - Dehydrogenation of gaseous hydrocarbons - Google Patents

Dehydrogenation of gaseous hydrocarbons

Info

Publication number
GB829760A
GB829760A GB29544/57A GB2954457A GB829760A GB 829760 A GB829760 A GB 829760A GB 29544/57 A GB29544/57 A GB 29544/57A GB 2954457 A GB2954457 A GB 2954457A GB 829760 A GB829760 A GB 829760A
Authority
GB
United Kingdom
Prior art keywords
oxide
catalyst
dehydrogenation
styrene
carrier
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
GB29544/57A
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
Publication of GB829760A publication Critical patent/GB829760A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/42Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74Iron group metals
    • C07C2523/745Iron

Landscapes

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

Abstract

In a process for the dehydrogenation of gaseous or vaporized hydrocarbons with ironoxide containing catalysts in a fluidized bed, wherein the liberated hydrogen combines with oxygen from the catalyst to form water, between 10-100 parts by weight, preferably 20-60 parts, of the catalyst are used to each part of the hydrocarbon, the catalyst is continuously removed from the reaction vessel, reheated and reoxidized and returned to the reaction vessel. For example, n-butene, isopentane, ethyl benzene, and isopropyl benzene may be respectively converted into butadiene, isoprene, styrene or methyl styrene in the reactor at 500-700 DEG C., preferably 550-650 DEG C., in the presence of water, with the iron oxide containing catalyst, for example with up to 15% of a spinel forming additive such as aluminium oxide, chromium oxide or copper oxide, with 3 to 10% of a promoter of chromium oxide, copper oxide or silver oxide and supported on a carrier of aluminium oxide, aluminium silicate, magnesium silicate, clay or bleaching earth. The catalyst is obtained by mixing the iron oxide, the additives, promoters and the carrier and firing the mass to give a product of up to 70%, preferably 30-60% of the carrier and of a grain size of 0.3-3 mm. In an example, styrene is obtained by introducing a mixture of 1 mol. of ethyl benzene and 10 mols. of water vapour into the bottom of the dehydrogenation reactor. The reactants fluidize the catalyst, comprising 50% (wt.) ferric oxide, 40% aluminium silicate and 10% kieselguhr, of particle size between 0.3 to 2 in the proportion of 50 parts by weight to 1 part of ethyl benzene to give a 55% dehydrogenation to styrene, the length of stay of the reactants in the reaction chamber being 0.7 sec. The temperature of the reaction chamber during dehydrogenation was 625 DEG C. and of the regeneration chamber was 740 DEG C., the heated catalytic material leaving the regeneration chamber being used to heat the water vapour entering the reaction vessel.ALSO:In a process for the dehydrogenation of gaseous or vaporized hydrocarbons with ironoxide containing catalysts in a fluidized bed, wherein the liberated hydrogen combines with oxygen from the catalyst to form water, between 10-100 parts by weight, preferably 20-60 parts, of the catalyst are used to each part of the hydrocarbon, the catalyst is continuously removed from the reaction vessel, reheated and reoxidized and returned to the reaction vessel. For example, n-butene, isopentane, ethyl benzene and isopropyl benzene may be respectively converted into butadiene, isoprene, styrene or methyl styrene in the reactor at 500-700 DEG C., preferably 550-650 DEG C., in the presence of water, with the iron oxide containing catalyst, for example with up to 15% of a spinel forming additive such as aluminium oxide, chromium oxide or copper oxide, with 3-10% of a promoter of chromium oxide, copper oxide or silver oxide and supported on a carrier of aluminium oxide, aluminium silicate, magnesium silicate, clay or bleaching earth. The catalyst is obtained by mixing the oxide, the additives, promoters and the carrier and firing the mass to give a product of up to 70%, preferably 30-60% of the carrier, and of a grain size between 0.3-3 mm. In an example, styrene is obtained by introducing a mixture of 1 mol. of ethyl benzene and 10 mols. of water vapour into the bottom of the dehydrogenation reactor. The reactants fluidize the catalyst, comprising 50% (wt.) ferric oxide 40% aluminium silicate and 10% kieselguhr, of particle size between 0.3-2 in the proportion of 50 parts by weight to 1 part of ethyl benzene to give a 55% dehydrogenation to styrene, the length of stay of the reactants in the reaction chamber being 0.7 secs. The temperature of the reaction chamber during dehydrogenation was 625 DEG C. and of the regeneration chamber was 740 DEG C., the heated catalytic material leaving the regeneration chamber being used to heat the water vapour entering the reaction vessel.
GB29544/57A 1956-09-24 1957-09-19 Dehydrogenation of gaseous hydrocarbons Expired GB829760A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE829760X 1956-09-24

Publications (1)

Publication Number Publication Date
GB829760A true GB829760A (en) 1960-03-09

Family

ID=6748591

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29544/57A Expired GB829760A (en) 1956-09-24 1957-09-19 Dehydrogenation of gaseous hydrocarbons

Country Status (1)

Country Link
GB (1) GB829760A (en)

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