生物炭
四溴双酚A
选择性
硫化
零价铁
电子转移
纳米尺度
降级(电信)
反应性(心理学)
材料科学
化学
无机化学
化学工程
纳米技术
催化作用
光化学
有机化学
硫黄
热解
吸附
阻燃剂
计算机科学
替代医学
病理
工程类
电信
医学
作者
Feilong Gao,Honghong Lyu,Shakeel Ahmad,Siyu Xu,Jingchun Tang
标识
DOI:10.1016/j.apcatb.2022.122246
摘要
A core-shell structure of sulfidated nanoscale zero-valent iron deposited on biochar (S-nZVI/BC) was synthesized and the performance of S-nZVI/BC on tetrabromobisphenol A (TBBPA) degradation was investigated. Detailed characterizations indicated that controlling S content altered distribution of S species (i.e., S2-, S22-, and Sn2-) in shell and core and achieved higher hydrophobicity and lower electron-transfer resistance. S-nZVI/BC was highly reactive (∼4.3–11.3 times) and selective (∼78.9–152.6 times) over nZVI/BC for TBBPA degradation. Besides, BC improved reactivity and selectivity of S-nZVI by 0.17 and 1.35 times, respectively, deriving from increased electron-transfer, enhanced hydrophobicity, and more surface reduced S species. Thus, sulfidation and BC enhanced reactivity and selectivity of S-nZVI/BC by combining respective merits. Effects of initial TBBPA concentration, pH, and particles dosage on TBBPA degradation by S-nZVI/BC were also investigated. Remarkably, mechanism investigation revealed that core properties instead of shell dominated reactivity and TBBPA debromination mainly involved direct electron-transfer rather than atomic H.
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