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铈促进的Ag/AlPO₄催化剂在水中利用分子氧的杀菌活性。

Bactericidal activity of a Ce-promoted Ag/AlPO4 catalyst using molecular oxygen in water.

作者信息

Chang Qingyun, He Hong, Zhao Jincai, Yang Min, Qut Jiuhui

机构信息

Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100080, China.

出版信息

Environ Sci Technol. 2008 Mar 1;42(5):1699-704. doi: 10.1021/es071810e.

Abstract

The catalytic inactivation of Escherichia coli in water by a cerium (Ce)-promoted silver-loaded aluminum phosphate (Ag/ AlPO4) catalyst using molecular oxygen was investigated. With optimum Ce content, the Ag(Ce)/AlPO4 catalyst exhibited strong bactericidal activity. The process of decomposition of the cell wall and cell membrane was directly observed by TEM. The different morphological changes of E. coli cells treated with the Ag(Ce)/AlPO4 catalyst and those treated with Ag+ suggested that the Ag+ eluted from the catalyst surface did not play an important role during the bactericidal process. Results of DMPO spin-trapping measurements by electron spin resonance (ESR) indicated the formation of the reactive oxygen species (ROS) *OH and *O2-, which caused the considerable bactericidal activity. The formation of H2O2 acted as an important intermediate; this was confirmed by addition of catalase as the scavenger. A possible catalytic oxidation bactericidal mechanism using molecular oxygen was proposed for the Ag(Ce)/AlPO4 catalyst.

摘要

研究了使用分子氧,通过铈(Ce)促进的负载银的磷酸铝(Ag/AlPO4)催化剂对水中大肠杆菌的催化失活作用。在最佳铈含量下,Ag(Ce)/AlPO4催化剂表现出很强的杀菌活性。通过透射电子显微镜(TEM)直接观察到细胞壁和细胞膜的分解过程。用Ag(Ce)/AlPO4催化剂处理的大肠杆菌细胞与用Ag+处理的细胞的不同形态变化表明,从催化剂表面洗脱的Ag+在杀菌过程中不起重要作用。电子自旋共振(ESR)进行的DMPO自旋捕获测量结果表明,活性氧(ROS)OH和O2-的形成导致了显著的杀菌活性。H2O2的形成作为一个重要中间体;通过添加过氧化氢酶作为清除剂得到了证实。提出了一种使用分子氧的Ag(Ce)/AlPO4催化剂的可能催化氧化杀菌机制。

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