化学
单线态氧
环境化学
降级(电信)
硫化物
环境修复
激进的
吸附
铜
多酚
氧气
硫化物矿物
污染
双锰矿
无机化学
光化学
氧化还原
污染物
硫化铜
硫黄
活性氧
硫化锌
没食子酸丙酯
反应机理
地下水修复
作者
Yangju Li,Hexian Qin,Dapeng Wu,Haoran DONG
标识
DOI:10.1021/acs.est.5c16502
摘要
Natural polyphenols are prevalent in aquatic environments, playing a critical role in the aerobic degradation of contaminants by redox-active minerals. Nevertheless, little is known about how the natural polyphenols influence the environmental behavior of copper sulfide minerals and reactive oxygen species (ROS) generation. In this work, the role of natural polyphenols in the degradation of waterborne emerging contaminants during CuS- x (a composite of Cu 2 S and CuS) oxygenation was investigated, where protocatechuic acid (PCA) was selected as a representative natural polyphenol. It was demonstrated that PCA could significantly enhance the degradation of target contaminant by substantially boosting surface-bound • OH ( • OH bound ) generation via a three-electron O 2 activation pathway. Experimental analysis and theoretical calculations unveiled that PCA favored the adsorption and activation of O 2 on the CuS- x surface, thus facilitating the formation of O 2 •– (an important precursor of both • OH and singlet oxygen ( 1 O 2 )). The contributions of 1 O 2 and • OH bound to contaminant degradation in the CuS- x /PCA system were 31.8% and 60.2%, respectively. Notably, besides PCA itself, the oxidation products (i.e., ortho-quinones and semiquinone radicals) and S vacancies also played a crucial role in accelerating the Cu redox cycle to activate O 2 . These findings provide valuable insights for advancing sulfide mineral-based green remediation technologies.
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