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Stirring time effect of silver nanoparticles prepared in glutathione mediated by green method

机译:绿色方法介导的谷胱甘肽中制备的银纳米颗粒的搅拌时间效应

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Background This study aims to investigate the influence of different stirring time for synthesis of silver nanoparticles in glutathione (GSH) aqueous solution. The silver nanoparticles (Ag-NPs) were prepared by green synthesis method using GSH as reducing agent and stabilizer, under moderate temperature at different stirring times. Silver nitrate (AgNO3) was taken as the metal precursor while Ag-NPs were prepared in the over reaction time. Results Formation of Ag-NPs was determined by UV–vis spectroscopy where surface plasmon absorption maxima can be observed at 344–354 nm from the UV–vis spectrum. The synthesized nanoparticles were also characterized by X-ray diffraction (XRD). The peaks in the XRD pattern confirmed that the Ag-NPs possessed a face-centered cubic and peaks of contaminated crystalline phases were unable to be located. Transmission electron microscopy (TEM) revealed that Ag-NPs synthesized were in spherical shape. Zeta potential results indicate that the stability of the Ag-NPs is increases at the 72 h stirring time of reaction comparison to GSH. The Fourier transform infrared (FT-IR) spectrum suggested the complexation present between GSH and Ag-NPs. The use of green chemistry reagents, such as peptide, provides green and economic features to this work. Conclusions Ag-NPs were successfully synthesized in GSH aqueous solution under moderate temperature at different stirring times. The study clearly showed that the Ag-NPs synthesized in the long times of stirring, thus, the kinetic of GSH reaction is very slow. TEM results shows that with the increase of stirring times the mean particle size of Ag-NPs become increases. The FT-IR spectrum suggested the complexation present between GSH and Ag-NPs. These suggest that Ag-NPs can be employed as an effective bacteria inhibitor and can be applied in medical field.
机译:背景本研究旨在研究不同搅拌时间对谷胱甘肽(GSH)水溶液中银纳米颗粒合成的影响。采用绿色合成法,以GSH为还原剂和稳定剂,在中等温度,不同搅拌时间下,制备了银纳米颗粒(Ag-NPs)。硝酸银(AgNO3)被用作金属前体,而在过度反应时间内制备了Ag-NPs。结果Ag-NPs的形成是通过紫外-可见光谱确定的,在该表面上,在紫外-可见光谱的344-354 nm处可以观察到最大的表面等离子体吸收。合成的纳米颗粒还通过X射线衍射(XRD)表征。 XRD图谱中的峰证实了Ag-NP具有面心立方,并且无法找到受污染的结晶相的峰。透射电子显微镜(TEM)显示合成的Ag-NP呈球形。 Zeta电势结果表明,与GSH相比,在72小时搅拌时间,Ag-NPs的稳定性增加。傅立叶红外光谱(FT-IR)提示GSH和Ag-NP之间存在络合物。绿色化学试剂(例如肽)的使用为这项工作提供了绿色和经济的特点。结论在适度的温度,不同的搅拌时间下,在GSH水溶液中成功合成了Ag-NPs。研究清楚地表明,Ag-NPs是在长时间搅拌下合成的,因此GSH反应的动力学非常缓慢。 TEM结果表明,随着搅拌时间的增加,Ag-NPs的平均粒径增大。 FT-IR光谱表明存在GSH和Ag-NP之间的络合。这些表明Ag-NPs可以用作有效的细菌抑制剂,并且可以在医学领域中应用。

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