Bentonite binding with mercury(II) ion through promotion of reactive oxygen species derived from manure-based dissolved organic matter

被引:0
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作者
Saeed Rehman
Sayyaf Yousaf
Quanyun Ye
Liu Chenhui
Muhammad Bilal
Ahson Jabbar Shaikh
Muhammad Saqib Khan
Sohail Anjum Shahzad
Pingxiao Wu
机构
[1] South China University of Technology,School of Environment and Energy
[2] COMSATS University Islamabad,Department of Environmental Sciences
[3] Abbottabad Campus,Department of Chemistry
[4] KPK,undefined
[5] University Road,undefined
[6] State Environmental Protection Key Laboratory of Environmental Pollution Health Risk Assessment,undefined
[7] South China Institute of Environmental Sciences,undefined
[8] Ministry of Ecology and Environment,undefined
[9] COMSATS University Islamabad,undefined
[10] Abbottabad Campus,undefined
[11] KPK,undefined
[12] University Road,undefined
[13] The Key Lab of Pollution Control and Ecosystem Restoration in Industry Clusters,undefined
[14] Ministry of Education,undefined
[15] Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling,undefined
[16] Guangdong Engineering and Technology Research Center for Environmental Nanomaterials,undefined
[17] Guangdong Provincial Engineering and Technology Research Center for Environmental Risk Prevention and Emergency Disposal,undefined
关键词
Bentonite binding; Manure DOM; Oxygen functional groups; Metal complex;
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学科分类号
摘要
This study reports the mercury binding by bentonite clay influenced by cattle manure–derived dissolved organic matter (DOM). The DOM (as total organic carbon; TOC) was reacted with bentonite at 5.2 pH to monitor the subsequent uptake of Hg2+ for 5 days. The binding kinetics of Hg2+ to the resulting composite was studied (metal = 350 µM/L, pH 5.2). Bentonite-DOM bound much more Hg2+ than original bentonite and accredited to the establishment of further binding sites. On the other hand, the presence of DOM was found to decrease the Hg2+ binding on the clay surface, specifically, the percent decrease of metal with increasing DOM concentration. Post to binding of DOM with bentonite resulted in increased particle size diameter (~ 33.37– ~ 87.67 nm) by inducing the mineral modification of the pore size distribution, thus increasing the binding sites. The XPS and FTIR results confirm the pronounced physico-chemical features of bentonite-DOM more than that of bentonite. Hydroxyl and oxygen vacancies on the surface were found actively involved in Hg2+ uptake by bentonite-DOM composite. Furthermore, DOM increased the content of Hg2+ binding by ~ 10% (pseudo-second-order qe = 90.9–100.0) through boosting up Fe3+ reduction with the DOM. The quenching experiment revealed that more oxygen functionalities were generated in bentonite-DOM, where hydroxyl was found to be dominant specie for Hg2+ binding. The findings of this study can be used as theoretical reference for mineral metal interaction under inhibitory or facilitating role of DOM, risk assessment, management, and mobilization/immobilization of mercury in organic matter–containing environment.
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页码:26107 / 26119
页数:12
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