Research Article
Influence of Molybdenum Content and MoO
−
Species on
the Textural and Structural ZrO
2
Properties
Alberto Hernández Zapién,
1
Juan Manuel Hernández Enríquez,
1
Ricardo García Alamilla,
1
Guillermo Sandoval Robles,
1
Ulises Páramo García,
1
and Luz Arcelia García Serrano
2
1
Instituto Tecnol´ ogico de Ciudad Madero, Divisi´ on de Estudios de Posgrado e Investigaci´ on, Juventino Rosas y Jes´ us Urueta s/n,
Colonia Los Mangos, 89440 Ciudad Madero, TAMPS, Mexico
2
Centro Interdisciplinario de Investigaciones y Estudios sobre Medio Ambiente y Desarrollo, 30 de Junio No. 1520,
Barrio La Laguna Ticom´ an, 07340 M´ exico, DF, Mexico
Correspondence should be addressed to Juan Manuel Hern´ andez Enr´ ıquez; jmanuelher@hotmail.com
Received 4 October 2014; Accepted 28 November 2014; Published 18 December 2014
Academic Editor: Bin Li
Copyright © 2014 Alberto Hern´ andez Zapi´ en et al. Tis is an open access article distributed under the Creative Commons
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is
properly cited.
Te present work proposes to study the incorporation of molybdenum into the zirconium oxide precursor (Zr(OH)
4
), in order to
analyze its possible repercussions on the textural and structural zirconia properties (ZrO
2
). For this, the Zr(OH)
4
was synthesized
by the sol-gel method and modifed with 5, 10, and 15 wt% of molybdenum into the stabilized oxide. Te synthesized materials
were dried at 120
∘
C for 24 h and then were calcined at 600
∘
C for 3 h. Te characterization of the solids was carried out by thermal
analysis, X-ray difraction, nitrogen physisorption, infrared spectroscopy, and scanning electron microscopy. Te thermal analyses
results showed that the change from the amorphous to the crystalline phase of ZrO
2
is shifed to higher temperatures due to the
presence of molybdenum content. Tetragonal phase was identifed for all synthesized materials, showing a decrease in crystallinity
as a function of the metal content. Te textural properties were improved due to the incorporation of molybdenum into the ZrO
2
structure, developing specifc surface areas which are above up to four times the area of pure ZrO
2
. Te synthesized materials
presented spherical morphology with particle sizes less than 1 m, with a change of this morphology for high metal contents (15
wt%) being observed.
1. Introduction
Catalysis is a crucial science for the chemical industry
development. About 80% of manufactured chemicals are
obtained by processes that require the use of a catalyst [1].
Specifcally, in the oil refning industry, in processes such
as isomerization and alkylation of light parafns, which
involve solid-gas reactions, require solid acid catalysts with
adequate specifc surface area and high thermal stability [2–
5], which may be improved by manipulating some variables
during the precursor synthesis. Zirconium oxide (ZrO
2
) has
been widely studied for this type of reactions because of
its acid-base properties [6–9]. Tis catalytic support can be
synthesized via precipitation, microemulsion, hydrothermal
synthesis, supercritical synthesis, pyrolysis, microwave, and
the sol-gel route [10–12]. Te sol-gel method has gained great
difusion since it allows preparing materials with high purity,
homogeneity, and controlled fnal properties [13, 14]. Te
precursor of zirconium oxide (Zr(OH)
4
) can be obtained
through the sol-gel method using metallic alkoxides, showing
high specifc surface area afer being synthesized; however
this parameter decreases by efect of thermal treatments to
which the material is subjected for obtaining the stabilized
oxide [15, 16] and this evinces its poor thermal stability. In
the literature it has been reported that the stability and the
specifc surface area of zirconium oxide are enhanced by the
addition of some promoter agents in its structure (SO
4
2−
,
PO
4
3−
,
and BO
3
3−
ions), which also stabilize the tetragonal
phase of ZrO
2
and improve their acidic properties [2, 17–
19]. However, the main disadvantage that arises when using
Hindawi Publishing Corporation
Advances in Materials Science and Engineering
Volume 2014, Article ID 432031, 8 pages
http://dx.doi.org/10.1155/2014/432031