Article ID Journal Published Year Pages File Type
68562 Journal of Molecular Catalysis A: Chemical 2006 28 Pages PDF
Abstract

This review paper presents the significant advances which were made in the last decade in the understanding of the transformation over acid and bifunctional zeolite catalysts of the cheap and readily available C2–C4 alkanes into more valuable products: mechanism of activation, reaction scheme, nature of the active sites. Both the transformations of pure alkanes: n-butane isomerization, C2–C4 alkane aromatization and of alkanes in mixture with alkenes: isobutane–butene alkylation or with aromatic hydrocarbons: benzene alkylation with ethane or propane are considered.

Graphical abstractThis review paper presents the significant advances which were made in the last decade in the understanding of the transformation over acid and bifunctional zeolite catalysts of the cheap and readily available C2–C4 alkanes into more valuable products. Thus, the bifunctional character of the complex aromatization pathway over Ga/HMFI catalysts is now well demonstrated: successive intervention of (probably bifunctional) species containing Ga for dehydrogenation steps and of protonic acid sites for oligomerization and cyclization steps. Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
Authors
, , , , , , ,