首页> 外文期刊>Reactive & Functional Polymers >Synthesis and characterization of poly(N-isopropylmethacrylamide-co- acrylic acid) microgels for in situ fabrication and stabilization of silver nanoparticles for catalytic reduction of o-nitroaniline in aqueous medium
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Synthesis and characterization of poly(N-isopropylmethacrylamide-co- acrylic acid) microgels for in situ fabrication and stabilization of silver nanoparticles for catalytic reduction of o-nitroaniline in aqueous medium

机译:聚(N-异丙基甲基丙烯酰胺-丙烯酸)微凝胶的合成与表征,用于在水介质中催化还原邻硝基苯胺的银纳米颗粒的原位制备和稳定化

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In this work, poly(N-isopropylmethacrylamide-co-acrylic acid) [p(NIPMAM-co-AAc)] microgels were synthesized by using precipitation polymerization method. Silver nanoparticles (AgNPs) were uniformly dispersed inside the sieves of the engineered microgels by in situ reduction method. Both microgels and hybrid microgels were characterized by Transmission Electron Microscopy (TEM), Ultraviolet-Visible (UV-Vis) spectroscopy and Fourier Transform Infrared (FTIR) spectroscopy. The average diameter of the fabricated AgNPs was found to be 15 nm. The catalytic reduction of 2-Nitroaniline (2-NA) was used as model reaction to investigate the catalytic activity of the hybrid microgels. The value of apparent rate constant (k(app)) for catalytic reduction of 2-NA was determined using pseudo first order kinetic model spectrophotometrically under various conditions of reaction to explore the mechanism of catalysis. The kinetic data reveals that catalytic reduction of 2-NA occurs according to Langmuir-Hinshelwood mechanism. The comparison of present study with previous literature makes our system a facile, efficient and stable catalyst for rapid and economical reduction of 2-NA in aqueous medium.
机译:在这项工作中,聚(N-异丙基甲基丙烯酰胺-共丙烯酸)[p(NIPMAM-co-AAc)]微凝胶通过沉淀聚合法合成。通过原位还原法将银纳米颗粒(AgNPs)均匀分散在工程化微凝胶的筛子中。通过透射电子显微镜(TEM),紫外可见(UV-Vis)光谱和傅立叶变换红外(FTIR)光谱对微凝胶和混合微凝胶进行了表征。发现制造的AgNP的平均直径为15nm。以2-硝基苯胺(2-NA)的催化还原为模型反应,以研究杂化微凝胶的催化活性。使用伪一级动力学模型在各种反应条件下分光光度法测定了2-NA催化还原的表观速率常数(k(app))的值,以探索催化机理。动力学数据表明,根据Langmuir-Hinshelwood机理发生了2-NA的催化还原。本研究与先前文献的比较使我们的系统成为快速,经济地还原水性介质中2-NA的简便,高效和稳定的催化剂。

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