The Pre-concentration and determination of Iridium and Palladium in environmental water by imprinted polymer-based method
In this study, the imprinted aniline-formaldehyde was used as an adsorbent for removal of Iridium and Palladium ions from aqueous solutions through batch equilibrium. The sorbent was characterized by fourier transform infrared spectroscopy. The influence of pH, equilibrium time, temperature and init...
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Veröffentlicht in: | International journal of environmental science and technology (Tehran) 2013-09, Vol.10 (5), p.1091-1102 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this study, the imprinted aniline-formaldehyde was used as an
adsorbent for removal of Iridium and Palladium ions from aqueous
solutions through batch equilibrium. The sorbent was characterized by
fourier transform infrared spectroscopy. The influence of pH,
equilibrium time, temperature and initial concentration of metal ions
on adsorbed amount of both ions were investigated. The maximum
adsorption capacity in initial concentration of 100 mg/L was found to
be 12.5 mg/g at pH 7.0 and 14.3 mg/g at pH 8.0 for Iridium and
Palladium, respectively. In addition, the best desorption of the metal
ions from resin was obtained by 0.5 mol/L nitric acid as eluting agent.
The profile of both ions uptake on this sorbent reflects good
accessibility of the chelating sites in the imprinted
aniline-formaldehyde. Langmuir, Freundlich, Temkin and Redlich-Peterson
isotherm models were applied to analyze the experimental data.
Moreover, Langmuir linear method was used to obtain the isotherm
parameters. However, Langmuir type II achieved the highest coefficient
which led to the best fit for the palladium and the best fit for
Iridium obtained from linear Redlich-Peterson. However, the
thermodynamic parameters (ΔG°, ΔH°, and
ΔS°) were also determined using the equilibrium constant
values obtained at different temperatures. The results showed that the
adsorption for Iridium and Palladium ions was spontaneous nature and
endothermic. Moreover, the method was applied for the determination of
both ions from tap water samples. |
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ISSN: | 1735-1472 1735-2630 |
DOI: | 10.1007/s13762-013-0308-y |