原位
方位(导航)
化学
半胱氨酸
环境化学
还原(数学)
核化学
生物化学
有机化学
地理
几何学
数学
酶
地图学
作者
Fei Wu,Jing Sun,Fangyuan Meng,Jimei Zhou,Qi Meng,Xiaoli Lu,Chengshuai Liu
标识
DOI:10.1016/j.watres.2024.122548
摘要
Structural Fe in phyllosilicates represents a crucial and potentially renewable reservoir of electron equivalents for contaminants reduction in aquatic and soil systems. However, it remains unclear how in-situ modification of Fe redox states within Fe-bearing phyllosilicates, induced by electron shuttles such as naturally occurring organics, influences the fate of contaminants. Herein, this study investigated the processes and mechanism of Cr(VI) reduction on two typical Fe(II/III)-bearing phyllosilicates, biotite and chlorite, in the presence of cysteine (Cys) at circumneutral pH. The experimental results demonstrated that Cys markedly enhanced the rate and extent of Cr(VI) reduction by biotite/chlorite, likely because of the formation of Cr(V)-organic complexes and consequent electron transfer from Cys to Cr(V). The concomitant production of non-structural Fe(II) (including aqueous Fe(II), surface bound Fe(II), and Cys-Fe(II) complex) cascaded transferring electrons from Cys to surface Fe(III), which further contributed to Cr(VI) reduction. Notably, structural Fe(II) in phyllosilicates also facilitated Cr(VI) reduction by mediating electron transfer from Cys to structural Fe(III) and then to edge-sorbed Cr(VI).
科研通智能强力驱动
Strongly Powered by AbleSci AI