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首页> 外文期刊>Journal of nanoparticle research: An interdisciplinary forum for nanoscale science and technology >Synthesis of iron nanoparticles in poly(N-isopropylacrylamide-acrylic acid) hybrid microgels for catalytic reduction of series of organic pollutants: a first approach
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Synthesis of iron nanoparticles in poly(N-isopropylacrylamide-acrylic acid) hybrid microgels for catalytic reduction of series of organic pollutants: a first approach

机译:聚(N-异丙基丙烯酰胺 - 丙烯酸)杂交微凝胶中铁纳米粒子的合成催化减少有机污染物的催化减少:第一种方法

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First approach towards in situ synthesis of iron (Fe) nanoparticles within poly(N-isopropylacrylamide-acrylic acid) (p(NIPAM-AA)) microgel is established in this work. Morphology, size, and size distribution of Fe-p(NIPAM-AA) hybrid microgel are confirmed by FTIR, STEM, and UV-Vis spectroscopy. Size of majority of Fe nanoparticles lies in 5-25-nm range, and very few nanoparticles lie in 30-40-nm range. Reduction of series of substrates with similar and dissimilar chemical structure is catalyzed by synthesized Fe-p(NIPAM-AA) hybrid microgel. Catalytic activity of hybrid microgel towards various substrates is studied by comparing their apparent rate constant (k(app)), reduction time, and percentage reduction. Catalytic activity of hybrid microgel towards reduction of nitroarenes is observed higher than that of azo dyes. Repulsion among carboxyl groups (COOH) of AA facilitated the flux of substrates inside the microgel network. Significant difference among k(app), reduction time, and percentage reduction of all substrates is observed. k(app) of crystal violet is observed maximum among all substrates. Percentage conversion of 4-nitroanisole is observed highest among all substrates. Similar values of k(app), reduction time, and reduction percentage of all nitrophenols are obtained, while significant difference in values of k(app), reduction time, and reduction percentage of all azo dyes is observed. Catalytic reduction of all substrates is compared on the basis of orientation of functional groups, presence of bulky groups, and number of bonds to be reduced.
机译:首先在该工作中建立了聚(N-异丙基丙烯酰胺 - 丙烯酸)(P(NIPAM-AA))微凝胶中的铁(Fe)纳米颗粒的第一方法。 Fe-P(NIPAM-AA)杂交微凝胶的形态,尺寸和尺寸分布通过FTIR,茎和UV-VIS光谱证实。大部分Fe纳米颗粒的大小位于5-25纳米范围内,很少有纳米颗粒位于30-40纳米范围内。通过合成的Fe-P(NIPAM-AA)杂交微凝胶催化具有相似且不同的化学结构的一系列衬底的减少。通过比较它们的表观速率常数(K(APP)),还原时间和减少百分比,研究了杂交微凝胶的催化活性。杂交微凝胶对硝基拉酮还原的催化活性高于偶氮染料。 AA的羧基(CoOH)之间的排斥促进了微凝胶网络内的基材的助焊剂。观察到所有基材的K(APP),还原时间和减少百分比之间的显着差异。在所有基材中最大地观察到晶体紫的K(APP)。在所有基材中观察到4-硝基吲哚的百分比转化。获得了所有硝基酚的K(APP),还原时间和减少百分比的类似值,而k(APP),还原时间和减少所有偶氮染料的百分比的显着差异。在官能团的取向的基础上,在官能团的取向,庞大基团的存在和减少的键数的基础上进行比较所有底物的催化还原。

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