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Zirconium(IV)
selenophosphate, a three-component inorganic ion-exchanger
was synthesized. In most cases, it was found that the ion-exchange
capacity of three-component inorganic ion-exchangers was greater
than those of two-component inorganic ion-exchangers. A theoretical
explanation was given for the enhancement of ion-exchanger
capacity of three-component materials and was found to be
in good agreement with the experimental value.
Various
synthetic inorganic ion-exchangers have been developed so
far mostly based on arsenate, phosphate, tungstate, molybdate
and selenite of metals (Qureshi and Rawat, 1968; Dyer and
Gill, 1970; Qureshi et al., 1970; Qureshi et al.,
1971; Qureshi and Nabi, 1971 and 1972; Singh et al.,
2003; and Gupta et al., 2004 and 2005). Three-component
inorganic ion-exchangers which were reported earlier (Qureshi
et al., 1976; Qureshi and Kaushik, 1977; Varshney and
Khan, 1979; Nabi et al., 1982; and Berardelli et
al., 1985) showed an increased ion-exchange capacity as
compared to the two-component materials (Nunes et al.,
1961; Amphlett, 1964; Inoue, 1964; Clearfield et al.,
1968; Qureshi and Varshney, 1968; Qureshi et al., 1970;
Qureshi et al., 1977; and Qureshi and Rahman, 1987).
However, no attempt has been made to explain the increased
ion-exchange capacity of these materials. In this paper, a
preliminary study has been done to explain the enhanced ion-exchange
capacity in terms of: (a) three-dimensional skeleton comprising
three different elements; (b) pK values of acid anionic group
incorporated into the lattice structure; and (c) pH titration.
The values so obtained are in good agreement with experimentally
reported ion-exchange capacities.
An
Elico model Li-10 pH meter (India) was used to measure pH
of the solutions. A Bausch and Lomb Spectronic 20 D+ (USA) and a Perkin Elmer 137 spectrophotometer (USA) were
used for absorbance and IR studies respectively.The
synthesis of zirconium(IV) selenophosphate ion-exchanger has
been synthesized in the laboratory (Qureshi and Rahman, 1987).
Samples of zirconium(IV) selenophosphate ion-exchangers were
synthesized by adding an aqueous solution which was 0.05 M
(1M = 1 mol dm-3) in sodium selenite and 0.05 M
in orthophosphoric acid to an aqueous solution of zirconium(IV)
bis (nitrate) oxide. The desired pH was adjusted by adding
dilute HNO3 or NaOH solution. The gel so formed
was allowed to settle down for 24 h, washed several times
with distilled water to remove excess reagents, and filtered
under suction. It was then dried at 40 °C for seven days
in an oven. The dried material was then treated with distilled
water, which resulted in the cracking of the substance into
smaller particles with slight evolution of heat. To convert
the sample into H+ form, the material was kept
for 24 h in 1.0 M HNO3 solution. It was then washed
with distilled water to remove excess acid.
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