Formation and Properties of Ni–Ce–La–O Catalysts of Reforming


Citar

Texto integral

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

Resumo

In order to stabilize in the support matrix highly dispersed nickel forms of the active component, which are characterized by thermal stability and high resistance to carbonization under conditions of hydrocarbon raw material reforming, the synthesis of Ni–Ce–La–O catalysts was carried out with varying composition (La/Ce = 0, 0.25, 1, 4), the preparation technique (the method of polymer ester precursors and incipient-wetness impregnation) and the calcination temperature (300–900°C) of the samples. The patterns in the formation of materials are studied and a comparative study of the physicochemical properties of materials by a complex of methods (low-temperature nitrogen adsorption, X-ray phase analysis, Raman spectroscopy, transmission electron microscopy, and temperature-programmed reduction with hydrogen) is carried out. It is shown that at La : Ce = 0–4, the materials after calcination at 300–500°C are solid solutions based on ceria (Ni–Ce–La–O, Ce–La–O) with deposited nickel oxide particles. Compared with impregnation, the method of polymer ester precursors provides a higher specific surface area and the defect structure of material, a smaller average crystallite size of the solid solution, and nickel stabilization mainly in the composition of a ceria-based solid solution. After high-temperature calcination at 700–900°C, the differences in the textural and structural characteristics of the catalysts prepared by different methods become less pronounced, which is due to the partial destruction of the Ni–Ce–La–O solid solution. It is found that an increase in the dispersion and thermal stability of the Ni-containing phase and a decrease in the degree of carbonization of the Ni–Ce–La–O catalysts in the ethanol autothermal reforming is achieved by increasing the La : Ce molar ratio and using the method of polymer ester precursors for the synthesis.

Sobre autores

E. Matus

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences; Novosibirsk State Technical University

Autor responsável pela correspondência
Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090; Novosibirsk, 630073

D. Nefedova

Novosibirsk State Technical University; Institute of Coal Chemistry and Material Science of FRC CCC, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk, 630073; Kemerovo, 650000

O. Sukhova

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090

I. Ismagilov

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090

V. Ushakov

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090

S. Yashnik

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090

A. Nikitin

Institute of Coal Chemistry and Material Science of FRC CCC, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Kemerovo, 650000

M. Kerzhentsev

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090

Z. Ismagilov

Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences; Institute of Coal Chemistry and Material Science of FRC CCC, Siberian Branch, Russian Academy of Sciences

Email: matus@catalysis.ru
Rússia, Novosibirsk,, 630090; Kemerovo, 650000

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Pleiades Publishing, Ltd., 2019