English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The obtained results show that styrene dimers, which are the primary transition products of PS cracking undergo consecutive reactions over acid centers of high acid strength (SiO–AlO(45 %); −10.8 < H ≤ −7.9) as well as centers of low acid strength (γ-AlO; H > −3.3) at sufficiently high reaction temperatures (723–773 K). It is proposed that phenylbutenyl carbenium ion obtained due to dealkylation reaction converts into coke by the successive elimination of H and H ions, which in turn take part in hydrogen transfer reactions resulting in the hydrogenation of styrene dimers to diphenylbutane. The dealkylation of this compound leads to active γ-butylbenzene carbenium ion which is a key intermediate for the formation of indane and naphthalene derivatives.

reaction kinetics, mechanisms and catalysis

The role of butylbenzene carbenium ions in the acid catalyzed cracking of polystyrene. Transformation of n-butylbenzene, sec-butylbenzene, iso-butylbenzene, tert-butylbenzene, 4-phenyl-1-butene, n-propylbenzene and n-hexylbenzene over silicaalumina and alumina acid catalysts