Enhanced molybdenum(VI) removal using sulfide-modified nanoscale zerovalent iron: kinetics and influencing factors

被引:5
|
作者
Lian, J. J. [1 ]
Yang, M. [1 ]
Wang, H. L. [2 ,4 ]
Zhong, Y. [2 ]
Chen, B. [1 ]
Huang, W. L. [3 ]
Peng, P. A. [2 ]
机构
[1] Anhui Univ Technol, Coll Energy & Environm, Maanshan 243002, Anhui, Peoples R China
[2] Chinese Acad Sci, Guangzhou Inst Geochem,State Key Lab Organ Geoche, Guangdong Hong Kong Macao Joint Lab Environm Poll, Guangdong Prov Key Lab Environm Protect & Resourc, Guangzhou 510640, Peoples R China
[3] Rutgers State Univ, Dept Environm Sci, 14 Coll Farm Rd, New Brunswick, NJ 08901 USA
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
adsorption; hexavalent molybdenum; nanoscale zero valent iron; reduction; sulfidation;
D O I
10.2166/wst.2020.570
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The overall goal of this study is to investigate the effect of sulfidated nanoscale zerovalent iron (S-nZVI) on the removal of hexavalent molybdate (MoO42-) under different aquatic chemistry conditions. Surface analysis suggests that Mo(VI) is removed mainly by adsorption and co-precipitation onto the surface of S-nZVI and a small amount of Mo(VI) can be reduced to Mo(V) species. The results of batch tests show that Mo(VI) removal by S-nZVI are well described with the pseudo-second-order adsorption model. The removal rate increases with a decrease in solution pH (4.0-9.0) and is significantly affected by the S/Fe ratio of S-nZVI, with the optimal S/Fe ratio being 0.5. The presence of anions WO42- or CrO42- can reduce the Mo(VI) removal, which is likely because they compete for adsorption sites on the solid surfaces. The divalent cations Ni2+, Cu2+ and Co2+ also inhibit the removal of Mo(VI) whereas Zn2+, Ca2+ and Mg2+ enhance it. After being aged for 35 d in water, S-nZVI still exhibits high reactivity towards Mo(VI) removal (57.39%). The study demonstrates that S-nZVI can be used as an environmentally friendly material for effectively removing Mo(VI) from contaminated water.
引用
收藏
页码:297 / 308
页数:12
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