Materials Science and Engineering B 178 (2013) 1076–1080
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Materials Science and Engineering B
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Short communication
Magnetic, oxidation and reduction behavior of spinel Ni–Cu
manganite Ni
x
Cu
1-x
Mn
2
O
4
powders
M.M. Rashad
a,∗
, M. Bahgat
a
, M. Rasly
a
, S.I. Ahmed
b
a
Central Metallurgical Research & Development Institute (CMRDI), P.O. Box: 87, Helwan 11421, Egypt
b
Department of Physics, Faculty of Science, Ain Shams University, Cairo, Egypt
a r t i c l e i n f o
Article history:
Received 19 February 2013
Received in revised form 24 June 2013
Accepted 27 June 2013
Available online 9 July 2013
Keywords:
Spinel manganite
CO oxidation
Reduction behavior
Magnetic properties
a b s t r a c t
Nickel copper manganites, Ni
x
Cu
1-x
Mn
2
O
4
(where 0 ≤ X ≤ 1), powders have been synthesized via co-
precipitation method. The formed particles were obtained from the precipitate precursors annealed at
800
◦
C for 2 h. The prepared powders were tested for the catalytic oxidation of carbon monoxide (CO)
into carbon dioxide (CO
2
). The results indicated that the intermediate compositions displayed better
catalytic activity than the end compositions for CO oxidation due to the phenomena of synergism. The
composition of x = 0.3 and 0.5 showed rapid rise in CO conversion with temperature; about 40% conversion
was achieved at 200
◦
C for the produced manganite sample of chemical composition Cu
0
.
7
Ni
0
.
3
Mn
2
O
4
.
A correlation between magnetic properties and hydrogen reduction of manganites was demonstrated.
Magnetic properties of reduced manganite were found to be duplicated. The saturation magnetization of
reduced NiMn
2
O
4
into Ni/MnO was duplicated of order 15 times from initial value.
© 2013 Elsevier B.V. All rights reserved.
1. Introduction
Emission of carbon monoxide gas in motor engines, industrial
process, and even by a burning cigarette is nowadays one of the
most significant environmental problems. A facile way to solve such
series environmental problem is to convert CO to CO
2
, which is less
harmful than carbon monoxide. Spinel manganites are widely used
as a catalyst for the oxidation of CO at ambient temperature, com-
bustion of many organic compounds including hydrocarbons, as
well as halide and nitrogen containing compounds [1–3]. They are
also important in respiratory protection, particularly in the min-
ing industry [4]. The oxidation process includes many chemical
and physical changes which take place simultaneously and have
a profound influence on the other. However, many investigators
studied kinetics and mechanism of CO oxidation to CO
2
[5–8], many
of the related phenomena are not yet fully understood. Therefore,
ways that can raise and monitor the catalytic activity of mangan-
ites even at low temperature is considered to be a topic of interest.
Comparatively, few works deal with magnetic properties of spinel
manganites, despite the fact that these materials are expected to
be rich in interesting phenomena. Their research has been focused
mainly on structural and electrical aspects [9]. Consequently, in
the present investigation an attempt has been made to study the
catalytic activity of introducing nickel into copper manganites for
∗
Corresponding author. Tel.: +202 5010642; fax: +202 25010639.
E-mail address: rashad133@yahoo.com (M.M. Rashad).
CO oxidation and pollution control. Moreover, the effect of hydro-
gen reduction on the microstructures and magnetic properties of
prepared manganites was also studied.
2. Experimental
2.1. Material synthesis
The co-precipitation method was employed to prepare sys-
tem of Ni
x
Cu
1-x
Mn
2
O
4
(X = 0, 0.3, 0.5, 0.7, and 1.0, respectively).
Appropriate amounts of Cu(NO
3
)
2
.6H
2
O, Ni(NO
3
)
2
.6H
2
O, and
Mn(NO
3
)
2
.4H
2
O were dissolved in deionized water. The manganite
precursors were precipitated using (5 M) sodium hydroxide solu-
tion as a base at pH value 10. The aqueous suspensions were stirred
at constant 500 rpm for 15 min to achieve good homogeneity and
attain a stable pH conditions. The co-precipitates were filtered off,
washed with deionized water and then dried in an oven at 100
◦
C
overnight. In order to form the manganite phase, the dry precursors
were annealed at 800
◦
C for 2 h.
2.2. Material characterization
The phases of the prepared and reduced powders were iden-
tified from the XRD patterns collected using a Brucker axis D8
diffractometer with Cu K
( = 1.5406
˚
A) radiation in 2 range from
10 to 80
◦
. The particle morphology was investigated by scanning
electron microscope (SEM JSM-5400). Specific surface area of the
produced samples was determined by BET surface area analyzer
0921-5107/$ – see front matter © 2013 Elsevier B.V. All rights reserved.
http://dx.doi.org/10.1016/j.mseb.2013.06.022