NL7111882A - Catalytic disproportionation of alkenes - using catalyst contg aluminium oxide tungsten and alkali metal - Google Patents

Catalytic disproportionation of alkenes - using catalyst contg aluminium oxide tungsten and alkali metal

Info

Publication number
NL7111882A
NL7111882A NL7111882A NL7111882A NL7111882A NL 7111882 A NL7111882 A NL 7111882A NL 7111882 A NL7111882 A NL 7111882A NL 7111882 A NL7111882 A NL 7111882A NL 7111882 A NL7111882 A NL 7111882A
Authority
NL
Netherlands
Prior art keywords
catalyst
esp
alkali metal
degrees
alkenes
Prior art date
Application number
NL7111882A
Other versions
NL145527B (en
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 filed Critical
Priority to NL717111882A priority Critical patent/NL145527B/en
Publication of NL7111882A publication Critical patent/NL7111882A/en
Publication of NL145527B publication Critical patent/NL145527B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • 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
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • 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
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/02Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the alkali- or alkaline earth metals or beryllium
    • C07C2523/04Alkali metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/24Chromium, molybdenum or tungsten
    • C07C2523/30Tungsten

Abstract

Catalytic disproportionation of gutene-2 and/or penten-2 with isobutene and/or a vinyl aromatic-type compd. using a catalyst consisting of at least 75 wt. % Al2O3 carrier, 7.0-9.0 (esp. 7.8-9.2) wt. % tungsten cpds. (as W) and alkali metal cpds. with an alkaline reaction, and having an atomic ratio alkali metal: W of 0.2-0.5 (esp. 0.3-0.4). Process is pref. carried out at 150-300 degrees C (esp. 210-240 degrees C) and 0.9-20 atm. abs., using 1-150 litres alkenes (as liquid) per litre catalyst. Disproportionation of isobutene with butene-2 gives propylene and 2-methylbutene-2 which can be dehydrogenated to isoprene. Styrene or alpha-methyl styrene disproportionated with butene-2 gives 1-phenylpropene-1 and 2-phenylbutene-2 respectively. Catalyst gives high yields and good selectivity with reduced by-product formation. Catalyst is made by impregnating the carrier with solutions of the tungsten and alklia metal (esp. potassium) compounds followed by drying and heat treating for 1-10 hrs. at 300-350 degrees C.
NL717111882A 1971-08-27 1971-08-27 METHOD FOR THE DISPROPORTION OF ALKINES. NL145527B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NL717111882A NL145527B (en) 1971-08-27 1971-08-27 METHOD FOR THE DISPROPORTION OF ALKINES.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL717111882A NL145527B (en) 1971-08-27 1971-08-27 METHOD FOR THE DISPROPORTION OF ALKINES.

Publications (2)

Publication Number Publication Date
NL7111882A true NL7111882A (en) 1972-05-25
NL145527B NL145527B (en) 1975-04-15

Family

ID=19813904

Family Applications (1)

Application Number Title Priority Date Filing Date
NL717111882A NL145527B (en) 1971-08-27 1971-08-27 METHOD FOR THE DISPROPORTION OF ALKINES.

Country Status (1)

Country Link
NL (1) NL145527B (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4419526A (en) * 1982-07-29 1983-12-06 Monsanto Company Catalyst and reverse disproportionation process
US4419527A (en) * 1982-07-29 1983-12-06 Monsanto Company Catalyst and reverse disproportionation process
US4439628A (en) * 1982-07-29 1984-03-27 Monsanto Company Catalyst and reverse disproportionation process
US4439626A (en) * 1982-07-29 1984-03-27 Monsanto Company Catalyst and reverse disproportionation process
US4440968A (en) * 1982-07-29 1984-04-03 Monsanto Company Catalyst and reverse disproportionation process
US4490477A (en) * 1982-07-29 1984-12-25 Monsanto Company Catalyst and reverse disproportionation process
US4511672A (en) * 1982-07-29 1985-04-16 Monsanto Company Catalyst and reverse disproportionation process
US4754099A (en) * 1987-05-27 1988-06-28 Shell Oil Company Disproportionation of olefins
US4962263A (en) * 1988-05-20 1990-10-09 Shell Oil Company Disproportionation of olefins
US5304692A (en) * 1991-10-17 1994-04-19 Maruzen Petrochemical Co., Ltd. Catalyst composition for disproportionation of olefins and process for disproportionation of olefins using the same

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4419526A (en) * 1982-07-29 1983-12-06 Monsanto Company Catalyst and reverse disproportionation process
US4419527A (en) * 1982-07-29 1983-12-06 Monsanto Company Catalyst and reverse disproportionation process
US4439628A (en) * 1982-07-29 1984-03-27 Monsanto Company Catalyst and reverse disproportionation process
US4439626A (en) * 1982-07-29 1984-03-27 Monsanto Company Catalyst and reverse disproportionation process
US4440968A (en) * 1982-07-29 1984-04-03 Monsanto Company Catalyst and reverse disproportionation process
US4490477A (en) * 1982-07-29 1984-12-25 Monsanto Company Catalyst and reverse disproportionation process
US4511672A (en) * 1982-07-29 1985-04-16 Monsanto Company Catalyst and reverse disproportionation process
US4754099A (en) * 1987-05-27 1988-06-28 Shell Oil Company Disproportionation of olefins
US4962263A (en) * 1988-05-20 1990-10-09 Shell Oil Company Disproportionation of olefins
US5304692A (en) * 1991-10-17 1994-04-19 Maruzen Petrochemical Co., Ltd. Catalyst composition for disproportionation of olefins and process for disproportionation of olefins using the same

Also Published As

Publication number Publication date
NL145527B (en) 1975-04-15

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