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Polymer-assisted in-situ thermal reduction of silver precursors: A solventless route for silver nanoparticles-polymer composites

机译:银前体的聚合物辅助原位热还原:银纳米颗粒 - 聚合物复合材料的无溶剂途径

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A simple one-step solventless in-situ reduction method was developed to prepare silver nanoparticle (AgNP) based polymer composites using different silver precursors and thermoplastic polymers. This method utilizes the mild reducing environment of thermoplastic polymer melts to convert silver precursors to AgNPs during the extrusion process. Complete reduction of Ag2O with broad AgNP size distribution (20 +/- 18 nm) in polyamide 6 (PA6) was obtained after 5 min processing. For same matrix, the uniformity of AgNPs improved significantly after 10 min processing time, associated with a slight increase in the particle diameter (26 +/- 9 nm). No significant impact of in-situ AgNP synthesis method on chemical and macromolecular characteristics of polyamide 6 was detected. When this method was used to synthesize AgNPs in polylactic acid and polypropylene, the influence of surface energy of polymer melt was evident. Reduction of Ag2O in polylactic acid (at 165 degrees C) was slower compared to PA6 and 95 +/- 3% Ag2O reduction was achieved after 10 min of processing. When polypropylene was used as the matrix, only 60% reduction of Ag2O was achieved, possibly due to poor wetting of the silver precursor, owing to the low surface energy of polypropylene. AgNP-PA6 composites were also successfully prepared using Ag2CO3 and Ag-palmitate as precursors. To demonstrate the potential application of such composites in food packaging, the silver release and antibacterial activity of AgNP-PA6 composite were also studied. Though the composites released 500 times less silver compared to the permitted limits of different safety standards, they exhibited an excellent antibacterial activity against a typical food pathogen (Listeria monocytogenes) already at a low level of AgNP loading i.e. 0.5 wt%.
机译:开发了一种简单的一步式无能原位还原方法以使用不同的银前体和热塑性聚合物制备基于银纳米颗粒(AgNP)的聚合物复合材料。该方法利用热塑性聚合物的温和还原环境熔化以在挤出过程中将银前体转化为AgNP。 5分钟加工后,得到了聚酰胺6(PA6)中具有宽AgNP尺寸分布(20 +/- 18nm)的Ag2O的Ag2O的完全降低。对于相同的基质,AgNP的均匀性在10分钟加工时间后显着改善,粒径略微增加(26 +/- 9nm)。检测到原位AGNP合成方法对聚酰胺6的化学和大分子特征没有显着影响。当该方法用于合成聚乳酸和聚丙烯中的AgNP时,聚合物熔体的表面能的影响很明显。与PA6和95 +/- 3%的加工后,在加工10分钟后达到相比,在聚乳酸酸(165℃)中的Ag 2 O的减少较慢。当聚丙烯用作基质时,由于聚丙烯的低表面能量,可能由于银前体的润湿性较差而获得了达到的Ag 2 O的60%。使用Ag2CO3和Ag-Palmitate作为前体成功制备AgNP-PA6复合材料。为了证明这种复合材料在食品包装中的潜在应用,还研究了AgNP-PA6复合材料的银释放和抗菌活性。虽然复合材料与不同安全标准的允许的允许的允许释放的银释放了500倍,但它们对典型的食物病原体(Listeria单核细胞增生)表现出优异的抗菌活性,其已经处于低水平的AgNP Lolbess i.0.5wt%。

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