Mori et al., 1993 - Google Patents

Liquid phase reaction of acetaldehyde over various ZSM-5 zeolites

Mori et al., 1993

Document ID
6471373169167033980
Author
Mori H
Yamazaki T
Ozawa S
Ogino Y
Publication year
Publication venue
Bulletin of the Chemical Society of Japan

External Links

Snippet

Acetaldehyde reacted over various ion-exchanged ZSM-5 zeolites at 15±0.5° C under a nitrogen pressure of 1× 105 Pa. The main products of the reaction were 2 α, 4 α, 6 α- trimethyl-1, 3, 5-trioxane (cis-paraldehyde) and its isomer, 2 α, 4 α, 6 β-trimethyl-1, 3, 5 …
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • 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

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