Silver nanoparticles on UiO-66 (Zr) metal-organic frameworks for water disinfection application

被引:12
|
作者
Chen, Hui [1 ]
Qiu, Chen [1 ]
Jiang, Yiran [1 ]
Liao, Xinyu [1 ]
Wu, Dan [1 ]
Shen, Mofei [1 ]
Ding, Tian [1 ]
机构
[1] Zhejiang Univ, Coll Biosyst Engn & Food Sci, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Metal-organic framework; Silver nanoparticles; Antibacterial effects; Water disinfection; SELECTIVE OXIDATION; BACTERIAL; PERMEABILITY; OZONE; BURN; IONS;
D O I
10.1016/j.fshw.2021.11.017
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Drinking water disinfection is an essential process to assure public health all over the world. In this study, silver nanoparticles (AgNPs) on UiO-66 (Zr) Metal-Organic Frameworks (Ag@UiO-66) is proposed as a potential water disinfection strategy. AgNPs are synthesized using polyvinyl pyrrolidone (PVP) as stabilizing agent, and sodium borohydride as reducing agent are subsequently embedded on UiO-66, a high-stability organometallic framework. The effect of premixing time, reaction time and reactant concentration on the loading rate of AgNPs on UiO-66 was investigated. The maximum load rate of AgNPs on UiO-66 could reach 13% when the premixing time is 3 h, the reaction time is 45 min and the concentration of AgNO3 is 10 mu g/mL. The formation of AgNPs loaded on UiO-66 was observed and confirmed with ultraviolet and visible spectrophotometry (UV-Vis), scanning electron microscopy (SEM), infrared emission spectroscopy (IES) and X-ray diffraction (XRD) analysis. Ag@UiO-66 exhibited strong antibacterial activity against both Gram -negative Escherichia coli and Gram-positive Staphylococcus aureus, with minimum inhibitory concentrations (MIC) of 64 and 128 mu g/mL, respectively. The germicidal efficacy of Ag@UiO-66 enhanced significantly as the temperature rose from 4 degrees C to 37 degrees C. The results indicate that Ag@UiO-66 is potential candidate as a feasible water disinfection material. (C) 2022 Beijing Academy of Food Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
引用
收藏
页码:269 / 276
页数:8
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