Issue 3, 2012

Iron phosphate as a novel sorbent for selective adsorption of chromium(iii) and chromium speciation with detection by ETAAS

Abstract

Iron phosphate (FePO4) is for the first time used as a novel sorbent for chromium(III) adsorption. The prepared FePO4 was characterized by means of FT-IR, SEM and surface charge analysis, and used for selective adsorption of chromium(III). At pH 5.9, ca.100% of Cr(III) (<5 μg L−1) was retained on the surface of the adsorbent, while at the same conditions the adsorption of Cr(VI) was negligible (<2%). Cr(III) was adsorbed with an ca. 62/1 selectivity over Cr(VI). The adsorption of Cr(III) fits Langmuir model, corresponding to a maximum adsorption capacity of 8.12 mg g−1. The retained Cr(III) could be readily recovered by 200 μL of aqueous mixture of 0.1% H2O2 + 0.05 mol L−1 NH3 as stripping reagent, giving rise to a recovery of 96.5%. The chromium in the eluate is quantified with detection by electrothermal atomic absorption spectrometry. A sample volume of 2000 μL creates an enrichment factor of 8.7, along with a detection limit of 0.02 μg L−1 (3σ, n = 9) and a RSD of 2.5% (0.5 μg L−1) within a linear calibration range of 0.05–2.5 μg L−1. Total chromium was determined after reduction of Cr(VI) to Cr(III) by hydroxylamine hydrochloride as a reducing reagent. The content of Cr(VI) was achieved by difference. The method was validated by analyzing chromium content in a certified reference material (GBW08608, Trace Elements in Water) and speciation of Cr(III) and Cr(VI) in sea water, tap water, spring water and ground water samples was conducted.

Graphical abstract: Iron phosphate as a novel sorbent for selective adsorption of chromium(iii) and chromium speciation with detection by ETAAS

Article information

Article type
Paper
Submitted
30 Sep 2011
Accepted
16 Dec 2011
First published
25 Jan 2012

J. Anal. At. Spectrom., 2012,27, 466-472

Iron phosphate as a novel sorbent for selective adsorption of chromium(III) and chromium speciation with detection by ETAAS

X. Zhang, S. Tang, M. Chen and J. Wang, J. Anal. At. Spectrom., 2012, 27, 466 DOI: 10.1039/C2JA10292G

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