化学
氢键
聚苯乙烯
光降解
吸附
光化学
傅里叶变换红外光谱
降级(电信)
化学工程
有机化学
分子
光催化
聚合物
催化作用
工程类
电信
计算机科学
作者
Lihua Bai,Sijia Liang,Hongjian Li,Chao Wang,Xinda Wu,Min Xu,Jiaqi Shi,Feng Zhu,Wei Chen,Cheng Gu
标识
DOI:10.1021/acs.est.4c11206
摘要
Fourier transform infrared spectroscopy, batch adsorption experiments, and theoretical calculations underscored that the structure-dependent enhancement stemmed from the specific hydrogen bonding sites, rather than mere adsorption capacity. Specifically, the -OOH group (hydroperoxyl group) on the PS surface exhibited a greater potential to generate OH• compared to the -OH group. Therefore, cephalosporins that formed hydrogen bonds with -OOH moieties on the aged PS surfaces, as opposed to -OH, would experience a more pronounced degradation enhancement. Thus, the unique interaction pattern between contaminants and PS-M/NPs transforms aged PS into a selective reactor, facilitating the targeted degradation of pharmaceuticals in aquatic ecosystems.
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