纳米银包埋聚合物复合材料的合成与表征

H. K. Chitte, N. Bhat, N. Karmakar, D. Kothari, G. N. Shinde
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引用次数: 49

摘要

采用化学还原法制备了纳米银。利用紫外可见光谱对银纳米粒子(AgNP)进行了表征,发现在420 nm处有一个吸收带,证实了纳米粒子的形成。对于银纳米粒子的任何实际应用来说,稳定它是必要的,这可以通过制造复合材料来实现。在目前的研究中,选择了三种聚合物,使AgNP可以投入一些实际应用。聚乙烯醇(PVA)、聚吡咯(Ppy)和羧甲基纤维素(CMC)分别在纺织、电子和食品/药物技术中具有重要用途。将聚乙烯醇(PVA)、聚吡啶(PPy)和CMC的水溶液与预成型纳米银的胶体悬浮液混合,制备了聚乙烯醇(PVA)、聚吡啶(PPy)和CMC的聚合物复合材料。制备了含有1% ~ 5%银纳米颗粒的各种组合物。利用紫外可见光谱、x射线衍射和扫描电镜对复合材料的薄膜进行了表征。x射线衍射表明,在2θ值为38.1°、44.2°、64.4°和78.2°处存在峰,对应于银金属的立方相。扫描电镜照片显示银纳米颗粒的存在,尺寸从40到80纳米不等。用四探针法研究了这些材料的电导率。电导率从对照样品的10-6 S/cm增加到纳米复合材料形成后的10-3 S/cm。
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Synthesis and Characterization of Polymeric Composites Embeded with Silver Nanoparticles
Silver nanoparticles were synthesized by chemical reduction method. The Ag nanoparticles (AgNP) were characterized using UV-Vis spectroscopy which shows an absorption band at 420 nm confirming the formation of nanoparticles. For any practical application of the silver nanoparticles it is necessary to stabilize it which can be done by making a composite. In the present studies three polymers were chosen such that AgNP could be put to some practical use. Polyvinyl Alcohol (PVA), Polypyrrole (Ppy) and Carboxymethyl cellulose (CMC) are important for use in textiles, electronics and food/drug technologies respectively. Polymeric composites of PVA, PPy, and CMC were prepared by mixing the aqueous solutions of the respective polymers and the colloidal suspension of preformed silver nanoparticles. Various compositions containing 1% to 5% of Ag nanoparticles were prepared. Thin films of these composites were characterized by UV-Vis spectroscopy, X-ray diffraction and Scanning electron microscopy. X-ray diffraction showed the presence of the peaks at 2θ values of 38.1°, 44.2°, 64.4 and 78.2° corresponding to cubic phase of silver metal. SEM photographs revealed the presence of Ag nanoparticles of sizes varying from 40 to 80 nm. The electrical conductivity of these materials was studied using the four probe method. The conductivity was found to increase from 10–6 for control samples to 10–3 S/cm after the formation of the nanocomposites.
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