GB592088A - Process for the conversion of normally gaseous olefins - Google Patents

Process for the conversion of normally gaseous olefins

Info

Publication number
GB592088A
GB592088A GB19620/44A GB1962044A GB592088A GB 592088 A GB592088 A GB 592088A GB 19620/44 A GB19620/44 A GB 19620/44A GB 1962044 A GB1962044 A GB 1962044A GB 592088 A GB592088 A GB 592088A
Authority
GB
United Kingdom
Prior art keywords
olefins
phosphoric acid
catalyst
paraffins
propylene
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
GB19620/44A
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.)
Universal Oil Products Co
Original Assignee
Universal Oil Products 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 Universal Oil Products Co filed Critical Universal Oil Products Co
Publication of GB592088A publication Critical patent/GB592088A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/10Catalytic processes with metal oxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • C07C2/14Catalytic processes with inorganic acids; with salts or anhydrides of acids
    • C07C2/18Acids of phosphorus; Salts thereof; Phosphorus oxides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/02Boron or aluminium; Oxides or hydroxides thereof
    • C07C2521/04Alumina
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • C07C2521/08Silica
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/14Phosphorus; Compounds thereof
    • C07C2527/16Phosphorus; Compounds thereof containing oxygen
    • C07C2527/167Phosphates or other compounds comprising the anion (PnO3n+1)(n+2)-
    • C07C2527/173Phosphoric acid or other acids with the formula Hn+2PnO3n+1

Abstract

Normally gaseous olefins are converted to hydrocarbons of higher molecular weight by contact with a polymerizing catalyst consisting of a solid phosphoric acid catalyst or a composite of silica with one or more of the oxides alumina, thoria, titania and zirconia under polymerizing conditions in the presence of an added substantially non - olefinic liquid hydrocarbon diluent comprising alkyl aromatic and/or naphthenic hydrocarbons which is substantially unreactive under the reaction conditions so that a substantially aliphatic product is formed. Preferably, a mixture of the hydrocarbon diluent with a minor proportion by weight of gaseous olefin is passed continuously at a space velocity of 2-4 liquid volumes per volume of catalyst space per hour, temperatures being about 200-500 DEG C., and pressures 13.5-70 atmos. Regulated p amounts of water or compounds yielding it may be added. Gas containing ethylene, propylene or butylene may be mixed with at least its own weight of a kerosene or other hydrocarbon which is largely of naphthenic and alkyl aromatic character and passed over a phosphoric acid-kieselguhr at about 300-400 DEG C. and 34 atmos. Ethylene is converted to paraffins and olefins of 4-8 carbon atoms including isobutane, butene, 2,3-dimethyl-butane and butene, while propylene yields similar products of 4-9 carbon atoms. Higher boiling products may remain in the liquid diluent which may be recycled or cracked to convert them to olefins for charging to the process. Olefins produced may be dehydrogenated to diolefins or isomerized while paraffins may also be dehydrogenated. In examples, a kerosene free from olefins and consisting largely of naphthenes, and alkyl aromatics and of less than 50 per cent paraffins is mixed with ethylene and treated with a solid phosphoric acid catalyst to yield a gas largely isobutane and butenes, and C5-C7 fractions, the C6 being mainly 2,3-dimethylbutene-2. Propylene is converted similarly using phosphoric acid-kieselguhr or silica-alumina as catalyst.
GB19620/44A 1943-09-16 1944-10-11 Process for the conversion of normally gaseous olefins Expired GB592088A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US592088XA 1943-09-16 1943-09-16

Publications (1)

Publication Number Publication Date
GB592088A true GB592088A (en) 1947-09-08

Family

ID=22021493

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19620/44A Expired GB592088A (en) 1943-09-16 1944-10-11 Process for the conversion of normally gaseous olefins

Country Status (1)

Country Link
GB (1) GB592088A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4977249A (en) * 1986-07-13 1990-12-11 Hodogaya Chemical Co., Ltd. Metal of hydroxy-phenylaze and hydroxy-naphthylazo compounds as near-red absorbers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4977249A (en) * 1986-07-13 1990-12-11 Hodogaya Chemical Co., Ltd. Metal of hydroxy-phenylaze and hydroxy-naphthylazo compounds as near-red absorbers

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