TY - JOUR
T1 - Adsorption of arsenite and selenite using an inorganic ion exchanger based on Fe–Mn hydrous oxide
AU - Szlachta, Małgorzata
AU - Gerda, Vasyl
AU - Chubar, Natalia
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledged KAUST grant number(s): KUK-C1-017-12
Acknowledgements: This work was funded by the Center-in-Development Award to Utrecht University (No. KUK-C1-017-12) by King Abdullah University of Science and Technology.Dr. Andrey Shchukarev (Umeä University, Sweden) is gratefully acknowledged for XPS analysis.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2012/1
Y1 - 2012/1
N2 - The adsorption behaviour and mechanism of As(III) and Se(IV) oxyanion uptake using a mixed inorganic adsorbent were studied. The novel adsorbent, based on Fe(III)-Mn(III) hydrous oxides and manganese(II) carbonate, was synthesised using a hydrothermal precipitation approach in the presence of urea. The inorganic ion exchanger exhibited a high selectivity and adsorptive capacity towards As(III) (up to 47.6mg/g) and Se(IV) (up to 29.0mg/g), even at low equilibrium concentration. Although pH effects were typical for anionic species (i.e., the adsorption decreased upon pH increase), Se(IV) was more sensitive to pH changes than As(III). The rates of adsorption of both oxyanions were high. Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) studies showed that the ion exchange adsorption of both anions took place via OH - groups, mainly from Fe(III) but also Mn(III) hydrous oxides. MnCO 3 did not contribute directly to As(III) and Se(IV) removal. A higher adsorptive capacity of the developed material towards As(III) was partly due to partial As(III) oxidation during adsorption. © 2011 Elsevier Inc.
AB - The adsorption behaviour and mechanism of As(III) and Se(IV) oxyanion uptake using a mixed inorganic adsorbent were studied. The novel adsorbent, based on Fe(III)-Mn(III) hydrous oxides and manganese(II) carbonate, was synthesised using a hydrothermal precipitation approach in the presence of urea. The inorganic ion exchanger exhibited a high selectivity and adsorptive capacity towards As(III) (up to 47.6mg/g) and Se(IV) (up to 29.0mg/g), even at low equilibrium concentration. Although pH effects were typical for anionic species (i.e., the adsorption decreased upon pH increase), Se(IV) was more sensitive to pH changes than As(III). The rates of adsorption of both oxyanions were high. Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) studies showed that the ion exchange adsorption of both anions took place via OH - groups, mainly from Fe(III) but also Mn(III) hydrous oxides. MnCO 3 did not contribute directly to As(III) and Se(IV) removal. A higher adsorptive capacity of the developed material towards As(III) was partly due to partial As(III) oxidation during adsorption. © 2011 Elsevier Inc.
UR - http://hdl.handle.net/10754/597473
UR - https://linkinghub.elsevier.com/retrieve/pii/S0021979711011362
UR - http://www.scopus.com/inward/record.url?scp=80054849391&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2011.09.023
DO - 10.1016/j.jcis.2011.09.023
M3 - Article
C2 - 21968401
SN - 0021-9797
VL - 365
SP - 213
EP - 221
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
IS - 1
ER -