n-Hexane Isomerization in the Presence of Nanodispersed Catalysts Supported on Acid-Activated Montmorillonite in the Sodium Form


Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Catalysts based on a palladium sol supported on acid-activated montmorillonite in the Na form (Pd-sol/NaHMM) have been tested in the n-hexane isomerization reaction. An increase in the Pd content from 0.1 to 0.35% leads to an increase in the catalyst activity. The C6+ isomer selectivity remains stable and fairly high: it is 94.6–98.0% in the presence of the catalysts with a Pd content of 0.1 or 0.35%, respectively. The maximum conversion of n-hexane over the 0.35%Pd catalyst is 52.6% at a temperature of 400°C; the addition of mordenite leads to a slight decrease in conversion to 50.9%. The maximum conversion at 400°C in the presence of the 0.1%Pd catalyst and the mordenite-modified catalyst is 45.0 and 50.4%, respectively. The maximum yield of isomeric hexanes over the zeolite-free 0.35%Pd and 0.1%Pd catalysts is 44.9 and 39.3%, respectively. In the presence of the mordenite-containing 0.35%Pd/NaHMM+HM catalyst and the low-percentage 0.1%Pd/NaHMM+HM catalyst, the C6 isomer yield is 44.3 and 43.0%, respectively. The amount of hydrocracking products does not exceed 0.7%. The particle size of the Pd sols is 3.5–5 nm, as determined on a JEM 2100 high-resolution transmission electron microscope. The elemental composition of the Pd-sol/NaHMM catalysts containing different amounts of palladium and the catalysts modified with mordenite has been determined by energy dispersive X-ray fluorescence spectroscopy.

Авторлар туралы

L. Dzhumabaeva

Sokolsky Institute of Fuel, Catalysis, and Electrochemistry; Satpayev National Research Technical University

Хат алмасуға жауапты Автор.
Email: djumabaevals@mail.ru
Қазақстан, Almaty; Almaty

N. Zakarina

Sokolsky Institute of Fuel, Catalysis, and Electrochemistry

Хат алмасуға жауапты Автор.
Email: nelly_zakarina@rambler.ru
Қазақстан, Almaty

V. Tret’yakov

MIREA Russian Technological University

Email: nelly_zakarina@rambler.ru
Ресей, Moscow

G. Yeligbayeva

Satpayev National Research Technical University

Email: nelly_zakarina@rambler.ru
Қазақстан, Almaty

D. Zhumadullaev

Sokolsky Institute of Fuel, Catalysis, and Electrochemistry

Email: nelly_zakarina@rambler.ru
Қазақстан, Almaty

T. Egorova

Moscow State University

Email: nelly_zakarina@rambler.ru
Ресей, Moscow

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