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Showing 2 results for Polyvinylpyrrolidone

P. Mouchani, R. Sarraf Mamoori, N. Riahi Noori,
Volume 35, Issue 4 (2-2017)
Abstract

In this study, the parameters affecting the synthesis of silver nanoparticles were optimized by green chemical reduction method to make a conductive pattern. The raw materials used in this study, include silver nitrate as a source of
silver ions, polyvinylpyrrolidone as surface stabilizer, and glucose as the reducing agent. Effective parameters were investigated
by Taguchi statistical design, to determine the optimum conditions and achieve the smallest average particle size. Silver nanoparticles were characterized by X-ray diffraction and field emission scanning electron microscopy. The smallest particle size can be applied by solution adding rate of 0.1 ml/min, temperature 90 °C, weight ratio of glucose to silver nitrate 3 g/g and weight ratio of Polyvinylpyrrolidone to silver nitrate 3.2 g/g. According to.our expectation 20 nm silver nanoparticles were obtained in this condition. FE-SEM confirmed the above results and showed nanoparticles with a size of 25 nm. Finally, A conductive pattern was printed on a glass substrate with synthesized powder. The electrical resistance of the printed pattern was 0.088× 10 -4 Ω.cm.


R. Karimi-Chaleshtori, M. R. Saeri, A. Doostmohammadi ,
Volume 40, Issue 1 (5-2021)
Abstract

Silver nanowires (AgNWs) are considered as one-dimensional nanostructures, which have received much attention due to their nanoscale size, high aspect ratio, high electrical and thermal conductivity, optical transparency and high mechanical stability. Preparation of AgNWs by polyol process is remarkably sensitive to the interactions between synthesis parameters. In this study, the effect of the simultaneous change of four synthetic parameters, namely the reaction temperature, the molecular weight of polyvinylpyrrolidone (PVP) stabilizer, the amount of sodium chloride, as well as, the solution mixing rate by the polyol process was reported. ­The results of field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM) confirmed that the synthesized AgNWs were below 100 nm. X-ray energy dispersive spectroscopy (EDS), ­X-ray diffraction (XRD) analysis, as well as, Fourier transform infrared spectroscopy (FT-IR) confirmed that the formed AgNWs were free of impurities. It was also found that temperature, molecular weight of PVP, salt concentration and solution mixing rate caused a significant change in the morphology of AgNWs. More importantly, a strong interaction was created in the preparation process of AgNWs by adjusting the parameters.


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