GB802559A - A dehydrogenation process - Google Patents

A dehydrogenation process

Info

Publication number
GB802559A
GB802559A GB39006/56A GB3900656A GB802559A GB 802559 A GB802559 A GB 802559A GB 39006/56 A GB39006/56 A GB 39006/56A GB 3900656 A GB3900656 A GB 3900656A GB 802559 A GB802559 A GB 802559A
Authority
GB
United Kingdom
Prior art keywords
catalyst
hydrocarbons
praseodymium oxide
alumina
silica
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
GB39006/56A
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.)
Heavy Minerals Co
Original Assignee
Heavy Minerals Co
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 Heavy Minerals Co filed Critical Heavy Minerals Co
Publication of GB802559A publication Critical patent/GB802559A/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
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/373Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
    • C07C5/393Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation with cyclisation to an aromatic six-membered ring, e.g. dehydrogenation of n-hexane to benzene
    • C07C5/41Catalytic processes
    • C07C5/412Catalytic processes with metal oxides or metal sulfides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/10Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of rare earths
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/321Catalytic processes
    • C07C5/322Catalytic processes with metal oxides or metal sulfides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/327Formation of non-aromatic carbon-to-carbon double bonds only
    • C07C5/333Catalytic processes
    • C07C5/3332Catalytic processes with metal oxides or metal sulfides
    • 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)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)

Abstract

Praseodymium oxide is prepared by precipitation of the hydroxide from a solution of the nitrate with caustic soda, washing the precipitate with water until free of ions and drying at 100-650 DEG C. in an inert gas. The product may be used alone or supported on alumina, magnesia, bauxite, mixtures of alumina and silica, silica gel or kieselguhr, after activation by heating to 430-650 DEG C. in nitrogen or hydrogen, as a catalyst in the vapour phase dehydrogenation of acyclic hydrocarbons (see Group IV (b)). The catalyst may be regenerated by treatment with air or other oxidizing gas at dehydrogenating temperatures.ALSO:Acyclic hydrocarbons are dehydrogenated in the presence of a catalyst containing praseodymium oxide (see Group III) at 430-650 DEG C. and a space velocity (liquid volume/catalyst volume/hour) of not more than 2.0. The hydrocarbons may be gaseous or liquid, straight or branched chain, C2-C12 aliphatic hydrocarbons. Pressures may be sub- or superatmospheric (e.g. 50-100 p.s.i.) but are preferably atmospheric. The catalyst may be praseodymium oxide, alone or supported on alumina, magnesia, bauxite, silica, kieselguhr or silicaalumina mixtures, and may be regenerated by oxidizing with air or other oxidizing gas at dehydrogenating temperatures. Naphthenes are not affected and aliphatic hydrocarbons may be selectively dehydrogenated in the presence of cyclic compounds. This selectivity may be used to separate saturated aliphatic hydrocarbons from naphthenes, the unsaturated aliphatic and aromatic hydrocarbons formed from the former being separated from the latter by conventional means such as by treatment with sulphuric acid, sulphur dioxide or absorption with silica gel. In an example, praseodymium oxide is used alone to dehydrogenate n-heptane at 525 DEG C. and a space velocity of 0.2. The product contains 12.4 per cent by weight olefines and 8.3 per cent by weight aromatics.
GB39006/56A 1956-05-23 1956-12-21 A dehydrogenation process Expired GB802559A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US802559XA 1956-05-23 1956-05-23

Publications (1)

Publication Number Publication Date
GB802559A true GB802559A (en) 1958-10-08

Family

ID=22156217

Family Applications (1)

Application Number Title Priority Date Filing Date
GB39006/56A Expired GB802559A (en) 1956-05-23 1956-12-21 A dehydrogenation process

Country Status (1)

Country Link
GB (1) GB802559A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4742180A (en) * 1984-04-16 1988-05-03 Atlantic Richfield Company Hydrocarbon dehydrogenation
GB2427574A (en) * 2005-06-24 2007-01-03 Ngimat Co Catalytic method of reducing sulphur content of a petroleum fluid and reforming a hydrocarbon to produce hydrogen
US7625482B1 (en) 2006-06-23 2009-12-01 Ngimat Co. Nanoparticulate-catalyzed oxygen transfer processes
CN114904507A (en) * 2022-06-15 2022-08-16 济南大学 Multifunctional praseodymium oxide nanorod catalyst for catalytic purification of diesel vehicle exhaust

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4742180A (en) * 1984-04-16 1988-05-03 Atlantic Richfield Company Hydrocarbon dehydrogenation
GB2427574A (en) * 2005-06-24 2007-01-03 Ngimat Co Catalytic method of reducing sulphur content of a petroleum fluid and reforming a hydrocarbon to produce hydrogen
GB2427574B (en) * 2005-06-24 2009-04-08 Ngimat Co Nanoparticulate-catalyzed oxygen transfer processes
US7625482B1 (en) 2006-06-23 2009-12-01 Ngimat Co. Nanoparticulate-catalyzed oxygen transfer processes
CN114904507A (en) * 2022-06-15 2022-08-16 济南大学 Multifunctional praseodymium oxide nanorod catalyst for catalytic purification of diesel vehicle exhaust

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