As(V) adsorption onto nanoporous titania adsorbents (NTAs): Effects of solution composition

被引:8
作者
Han, Dong Suk [1 ]
Batchelor, Bill [2 ]
Park, Sung Hyuk [3 ]
Abdel-Wahab, Ahmed [1 ]
机构
[1] Texas A&M Univ, Chem Engn Program, Doha 23874, Qatar
[2] Texas A&M Univ, Zachry Dept Civil Engn, College Stn, TX 77843 USA
[3] GS Engn & Construct Res Inst, Environm & Energy Res Team, Youngin Si 449831, Kyunggi Do, South Korea
关键词
Arsenate; Phosphate; Adsorption; Nanoporous adsorbent; Titania; SBA-15; MESOPOROUS SILICA; PHOTOCATALYTIC ACTIVITY; ARSENATE ADSORPTION; SIZE; REMOVAL; SBA-15; NANOPARTICLES; MECHANISMS; ARSENITE; KINETICS;
D O I
10.1016/j.jhazmat.2012.05.105
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study has focused on developing two nanoporous titania adsorbents (NTA) to enhance removal efficiency of adsorption process for As(V) by characterizing the effects of pH and phosphate concentration on their sorption capacities and behaviors. One type of adsorbent is a mesoporous titania (MT) solid phase and the other is group of a highly ordered mesoporous silica solids (SBA-15) that can incorporate different levels of reactive titania sorption sites. Microscopic analysis showed that Ti-(25)-SBA-15 (Ti/SBA = 0.25 g/g) had titania nanostructured mesopores that do not rupture the highly ordered hexagonal silica framework. However, MT has disordered, wormhole-like mesopores that are caused by interparticle porosity. Adsorption experiments showed that Ti-(25)-SBA-15 had a greater sorption capacity for As(V) than did Ti-(15)-SBA-15 or Ti-(35)-SBA-15 and the amount of As(V) adsorbed generally decreased as pH increased. Higher removal of As(V) was observed with Ti-(25)-SBA-15 than with MT at pH 4, but MT had higher removals at higher pH (7, 9.5), even though MT has a lower specific surface area. However, in the presence of phosphate, MT showed higher removal of As(V) at low pH rather than did Ti-(25)-SBA-15. As expected, the NTAs showed very fast sorption kinetics, but they followed a bi-phasic sorption pattern. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:273 / 281
页数:9
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