Aluminosilicates with different pores structure in the synthesis of 2,2,4-trimethyl-1,2-dihydroquinoline and N-phenyl-2-propanimine


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

Physicochemical characteristics of microporous zeolites of various structural type (FAU, BEA, MTW), micro-meso-macroporous zeolite (H-Ymmm), and mesoporous aluminosilicate (ASM) were studied. Their catalytic activity in the reaction of aniline with acetone was examined. It was found that 2,2,4-trimethyl-1,2-dihydroquinoline was the main reaction product on the catalysts H-Ymmm and ASM (selectivity up to 68% at 100% conversion of aniline), while the reaction on zeolites with microporous structure mainly gave N-phenyl-2-propanimine (selectivity up to 91%).

Sobre autores

N. Grigor’eva

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Autor responsável pela correspondência
Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

N. Filippova

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

A. Gataulin

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

S. Bubennov

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

M. Agliullin

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

B. Kutepov

Institute of Petrochemistry and Catalysis, Russian Academy of Sciences

Email: ngg-ink@mail.ru
Rússia, 141 prosp. Oktyabrya, Ufa, 450075

Nama Narender

CSIR-Indian Institute of Chemical Technology Uppal Road

Email: ngg-ink@mail.ru
Índia, Tarnaka, Hyderabad, Telangana State, 500 007

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Springer Science+Business Media, LLC, part of Springer Nature, 2017