Adsorption capacity of iron oxyhydroxide-coated brick for cationic metals and nature of ion-surface interactions

被引:21
作者
Allandin, O. [1 ]
Wartel, M. [2 ]
Recourt, P. [3 ]
Revel, B. [4 ]
Ouddane, B. [2 ]
Billon, G. [2 ]
Mabingui, J. [1 ]
Boughriet, A. [2 ,5 ]
机构
[1] Univ Bangui, Fac Sci, Lab Hydrosci Lavoisier, Chaire Unesco Gest Leau, Bangui, Cent Afr Republ
[2] Univ Lille 1, Lab Geosyst Equipe Chim Analyt & Marine, UMR CNRS 8217, F-59655 Villeneuve Dascq, France
[3] Univ Lille 1, Lab Geosyst, UMR CNRS 8217, F-59655 Villeneuve Dascq, France
[4] Univ Sci & Technol Lille 1, Serv RMN Resonance Magnet Nucl, F-59655 Villeneuve Dascq, France
[5] Univ Lille Nord France, IUT Bethune, Dept Chim, F-62408 Bethune, France
关键词
Brick; Ferrihydrite; Metals; Adsorption; NMR (Na-23 and H-1); ESM/EDS; LOW-COST ADSORBENTS; NMR CHEMICAL-SHIFTS; ZINC SORPTION; OXIDE; COMPLEXATION; PB(II); REMOVAL; CD(II); ZN(II); NI(II);
D O I
10.1016/j.clay.2014.01.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption of six metal ions (Cd2+, Cu2+, Fe2+, Ni2+, Pb2+ and Zn2+) from an aqueous solution by a new composite - iron oxyhydroxide (ferrihydrite) deposited onto pre-activated brick grains - was investigated under dynamic experimental conditions. Breakthrough curves were obtained under specified fixed-bed-column conditions, and the determined adsorption capacity (molar basis), Q followed the order of QPb(II) > QCd(II) approximate to QZn(II) > QFe(II) > QNi(II) > QCu(II). An attempt was made to correlate the ionic characteristics of these cationic metals with adsorption performance, and data revealed how strongly metal cations were attracted to negatively charged brick sites via electrostatic interactions. In addition to electrostatic attractions, a process implicating outer-sphere complexes, S-Na(H2O)(6)(+) and inner-sphere complexes, ( S-)(2)Me2+ (Me = metal), was suggested. ESEM/EDS analysis showed that cations were preferentially sorbed by ferrihydrite, rather than other hydroxyl groups in brick clays. A correlation also was found between the hydration free energy of Me2+ ions and hydrated radius, raising the possibility of water molecules being implicated in this adsorption mechanism. To confirm this hypothesis, Na-23 and H-1 MAS NMR were applied to our samples in order to examine the bonding states of sodium and water molecules and their dynamics at the material surface. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 149
页数:9
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