NDLI: Distribution of copper- and nickel-containing modifier components in the pore space of HZSM-5 zeolite

Content Provider	Springer Nature Link
Author	Gavrilov, V. Yu. Krivoruchko, O. P. Larina, T. V. Molina, I. Yu. Shutilov, R. A.
Copyright Year	2010
Abstract	The distribution of copper- and nickel-containing components in the pore space of HZSM-5 zeolite was quantitatively studied. It was found that the detailed distribution of a modifier in the micropore and mesopore volumes of the zeolite depends on both the chemical nature of the modifier and the conditions of supporting and the regime of M$^{2+}$ polycondensation in the pore space of the zeolite. The experimental data on the low-temperature adsorption of nitrogen on Cu(n)ZSM-5 catalysts can be interpreted as the result of the partial filling of the zeolite micropore space (10 vol %) and the finest mesopores with D < 3 nm with the modifier. In the case of Ni(n)ZSM-5 catalysts, the penetration of the modifier into zeolite channels (micropores) in detectable amounts was not found, and it was arranged in mesopores on the surface of zeolite crystallites. The reason for differences between modifier distributions in the pore structure of the zeolite was explained from the standpoint of different structures of copper and nickel polyhydroxo complexes in impregnating solutions after polycondensation. It was found that, in the Cu(n)ZSM-5 and Ni(n)ZSM-5 catalysts, the modifier component contained copper and nickel only in a doubly charged state and mainly octahedral oxygen environments. In this case, three-dimensional nanoparticles or coarsely dispersed particles of CuO were not detected in the pore space of the support, whereas the presence of a small amount of sufficiently large NiO crystals with a coherent-scattering region of 80–100 nm was detected in Ni(n)ZSM-5, and these crystals occurred on the surface of zeolite crystals. It was found that the apparent density of a copper-or nickel-containing component arranged in the pore space of the zeolite was lower than the density of the bulk CuO and NiO phases by a factor of ∼3 and 4, respectively, because of the size effect.
Starting Page	88
Ending Page	97
Page Count	10
File Format	PDF
ISSN	00231584
Journal	Kinetics and Catalysis
Volume Number	51
Issue Number	1
e-ISSN	16083210
Language	English
Publisher	SP MAIK Nauka/Interperiodica
Publisher Date	2010-03-17
Publisher Place	Dordrecht
Access Restriction	One Nation One Subscription (ONOS)
Subject Keyword	Physical Chemistry Catalysis
Content Type	Text
Resource Type	Article
Subject	Chemistry Catalysis Modeling and Simulation Computer Science Applications

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