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FeS–biochar and Zn(0)–biochar for remediation of redox-reactive contaminants

机译:FeS-Biochar和Zn(0)-biochar用于修复氧化还原反应性污染物

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摘要

To enhance the removal of redox-reactive contaminants, biochars including FeS and Zn(0) were developed via pyrolysis. These biochars significantly promoted the removal of 2,4-dichlorophenol (DCP) by means of sorption and reduction. Compared to direct reduction with FeS and Zn(0), the formation of reduction intermediates and product was enhanced from 21% and 22% of initial DCP concentration to 41% and 52%, respectively. 2,4-Dinitrotoluene (DNT), chromate (CrO _(4) ~(2?) ) and selenate (SeO _(4) ~(2?) ) were also reductively transformed to reduction products ( e.g. , 2,4-diaminotoluene [DAT], Cr ~(3+) , and selenite [SeO _(3) ~(2?) ]) after they sorbed onto the biochars including FeS and Zn(0). Mass recovery as DAT, Cr ~(3+) and selenite was 4–20%, 1–3%, and 10–30% under the given conditions. Electrochemical and X-ray analyses confirmed the reduction capability of the biochars including FeS and Zn(0). Fe and S in the FeS–biochar did not effectively promote the reductive transformation of the contaminants. Contrastingly, the stronger reducer Zn(0) yielded faster reductive transformation of contaminants over the Zn(0)-containing biochar, while not releasing high concentrations of Zn ~(2+) into the aqueous phase. Our results suggest that biochars including Zn(0) may be suitable as dual sorbents/reductants to remediate redox-reactive contaminants in natural environments.
机译:为了增强氧化还原反应性污染物的去除,通过热解显好地显影了包括FES和Zn(0)的生物脉。这些Biochars通过吸附和还原显着促进除去2,4-二氯苯酚(DCP)。与FES和Zn(0)的直接降低相比,将还原中间体和产物的形成分别从初始DCP浓度的21%和22%增强至41%和52%。 2,4-二硝基甲苯(DNT),铬酸盐(CRO _(4)〜(2?))和硒酸盐(SEO _(4)〜(2?))也被重新转化为还原产品(例如,2,4-二氨基甲苯[DAT],Cr〜(3+)和硒矿[SEO _(3)〜(2?)])在其吸附到包括FES和Zn(0)的生物脉冲之后。随着DAT,Cr〜(3+)和硒酸盐的质量恢复为4-20%,1-3%和10-30%在给定的条件下。电化学和X射线分析证实了包括FES和Zn(0)的Biochars的减少能力。 FES-Biochar中的FE和S没有有效促进污染物的还原转化。比较方面,较强的减速剂Zn(0)在Zn(0) - 甲型生物炭上产生更快的污染物的还原转化,同时不会将高浓度的Zn〜(2+)释放到水相中。我们的研究结果表明,包括Zn(0)的生物触体可能适合作为双吸附剂/还原剂来修复自然环境中的氧化还原活性污染物。

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