Preparation of High-Performance CdS@C Catalyst Using Cd-Enriched Biochar Recycled From Plating Wastewater

被引:23
作者
Xing, Rui-Zhi [1 ]
Li, Jia-Xin [1 ]
Yang, Xing-Gui [1 ]
Chen, Ze-Wei [1 ]
Huang, Rong [1 ]
Chen, Zhi-Xuan [1 ]
Zhou, Shun-Gui [1 ]
Chen, Zhi [1 ]
机构
[1] Fujian Agr & Forestry Univ, Coll Resources & Environm, Fujian Prov Key Lab Soil Environm Hlth & Regulat, Fuzhou, Peoples R China
基金
中国博士后科学基金;
关键词
biochar; photocatalyst; adsorption; cadmium sulfide; hazardous waste; HEAVY-METALS; PHOTOCATALYTIC DEGRADATION; HYPERACCUMULATOR PLANTS; HYDROGEN EVOLUTION; CADMIUM; ADSORPTION; REMOVAL; GRAPHENE; DOTS; H-2;
D O I
10.3389/fchem.2020.00140
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biochar is widely used for the adsorptive removal of Cd from water and soil, but the Cd-enriched biochar produced carries a risk of secondary pollution. In this work, biochar derived from rice straw was used to adsorb Cd from plating wastewater. The Cd-enriched biochar showed a saturated adsorption capacity of about 63.5 mg/g and could be recycled and used in a mesoporous carbon-supported CdS (CdS@C) photocatalyst after pyrolysis carbonization and a hydrothermal reaction. The results demonstrated that the as-prepared CdS@C photocatalyst contained mixed cubic and hexagonal CdS phases, with a considerably lower band gap (2.1 eV) than pure CdS (2.6 eV). CdS@C exhibited an enhanced photocatalytic performance for the degradation of organic dyes under visible light irradiation compared with pure CdS due to its excellent light-harvesting capacity and efficient electron-hole separation. Moreover, the continuous formation of active species (h(+), center dot OH, and O-2 center dot(-)) was responsible for the photodegradation of organic dyes using CdS@C. This work provides new insights for the safe disposal of Cd-enriched wastewater and for improving the economic viability of Cd-contaminated resources by recovering a value-added photocatalyst.
引用
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页数:9
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