环境修复
甲基汞
Mercury(编程语言)
生物累积
硫黄
污染
化学
环境化学
原位
吸附
甲基化
土壤水分
无机化学
生物化学
环境科学
有机化学
氢氧化物
计算机科学
生态学
土壤科学
基因
程序设计语言
生物
作者
Xin Tong,Zhanhua Zhang,Xiaoyin Dong,Wenyu Guan,Zhenhai Liu,Jiubin Chen,Pedro J. J. Alvarez,Wei Chen,Tong Zhang
标识
DOI:10.1021/acs.est.4c06870
摘要
Conventional approaches for in situ remediation of mercury (Hg)-contaminated soils and sediments rely mostly on precipitation or adsorption. However, this can generate Hg-rich surfaces that facilitate microbial production of methylmercury (MeHg), a potent, bioaccumulative neurotoxin. Herein, we prove the concept that the risk of mercury methylation can be effectively minimized by adding sulfur-intercalated layered double hydroxide (S-LDH) to Hg-contaminated soils. Hg bound to S-LDH has minimal methylation potential when incubated with model methylating bacteria Pseudodesulfovibrio mercurii ND132 and Geobacter sulfurreducens PCA. With a combination of spectroscopic and microscopic evidence, as well as theoretical calculations, we confirm that dissolved Hg(II) tends to enter the interlayers of S-LDH to bind to the sulfur groups intercalated within, leading to the formation of nanoscale metacinnabar (β-HgS). This not only physically blocks the contact of methylating microorganisms but also inhibits secondary release of bound mercury in the presence of strong binding ligands in porewater. This study highlights the promising concept of in situ risk reduction of heavy metal contamination by inducing precipitation within (nano)confined domains, achieving a sustainable outcome of enhanced removal and reduced bioaccessibility for pollutants that may otherwise be bioavailable in the form of nanoprecipitates.
科研通智能强力驱动
Strongly Powered by AbleSci AI