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Promotion effect of Mn2+ and Co2+ on selenate reduction by zero-valent iron
被引:34
|作者:
Tang, Cilai
[1
,2
]
Huang, Yong H.
[2
]
Zeng, Hui
[2
]
Zhang, Zengqiang
[3
]
机构:
[1] China Three Gorges Univ, Coll Hydraul & Environm Engn, Dept Environm Engn, Yichang 443002, Hubei, Peoples R China
[2] Texas A&M Univ, Dept Biol & Agr Engn, College Stn, TX 77843 USA
[3] Northwest A&F Univ China, Coll Resources & Environm, Yangling 712700, Shaanxi, Peoples R China
关键词:
Zero-valent iron;
Selenate removal;
Cobalt;
Manganese;
SELENIUM;
REMOVAL;
WATER;
NANOPARTICLES;
GROUNDWATER;
ADSORPTION;
IONS;
REMEDIATION;
DESORPTION;
MANGANESE;
D O I:
10.1016/j.cej.2014.01.059
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Our previous work demonstrated that Fe2+ could overcome the passivation of zero-valent iron (ZVI or Fe-0) and sustain iron reactivity for rapid selenate reduction. Due to the similar chemical properties to Fe2+ and co-existence in ZVI material as impurities, Mn2+ and Co2+ were evaluated as an alternative in selenate removal by ZVI. The results of batch experiments showed that Co2+ and Mn2+, especially the former, significantly enhanced selenate removal by ZVI. Co2+ promoted Fe2+ release and the formation of a bimetallic (Co-0-Fe-0) catalytic system by redox reaction. Co2+ and Mn2+ provided around 69% and 30% electron for selenate reduction, respectively. Selenite (Se-IV) was the predominant reductive product in the presence of Co2+; however, selenite and elemental Se (Se-0) were the main reductive products in the presence of Mn2+. Adsorbed selenate and selenite could be further reduced to elemental Se and even selenide by ZVI in the presence of Co2+ and Mn2+, identified by XPS analysis and sequential extraction test. The roles and evolution of Co2+ and Mn2+, and selenate removal mechanism were also comprehensively investigated by spectroscopic and chemical analysis. This study indicates that the co-existent of Co2+ and Mn2+ would be positive for selenate removal. (C) 2014 Elsevier B.V. All rights reserved.
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页码:97 / 104
页数:8
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