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Counter Anion-Directed Growth of Iron Oxide Nanorodsin a Polyol Medium with Efficient Peroxidase-Mimicking Activity forDegradation of Dyes in Contaminated Water

机译:反阴离子定向生长的氧化铁纳米棒在具有高效过氧化物酶模拟活性的多元醇培养基中污水中染料的降解

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摘要

Development of nanozymes, which are nanomaterials with intrinsic enzymatic properties, has emerged as an appealing alternative to the natural enzymes with tremendous application potential from the chemical industry to biomedicine. The self-assembled growth of micrometer-sized oxide materials with controlled nonspherical shapes can be an important tool for enhancing activity as artificial enzymes, as the formation of these superstructures often results in high surface area with favorable impact on catalytic activity. Herein, the growth of rod-shaped Fe3O4 microstructures via a one-pot microwave-based method and using a water–poly(ethylene glycol) mixture as a solvent is reported, without the involvement of external shape-directing agents. The precursor metal salt played a key role in the size, shape, and phase selective evolution of iron oxide microanomaterials. Whereas self-assembled microrod superstructures were obtained using Fe(NO3)3 as the metal salt precursor, use of FeCl3 or Fe-acetate as precursors afforded hollow Fe2O3 microparticles and Fe3O4 nanoparticles, respectively. A graphitic layer was deposited on the Fe3O4 surface, imparting a negative surface charge as a result of a high-temperature treatment of poly(ethylene glycol). The rod-shaped Fe3O4 microcrystals show efficient peroxidase-mimickingactivity toward 3,3,5,5′-tetramethylbenzidine and pyrogallolas peroxidase substrates with a Michaelis–Menten rate constant(Km) value of 0.05 and 0.52 mM, respectively.The proficient enzyme mimicking behavior of these magnetic superstructureswas further explored for the degradation of organic dyes that includesrhodamine B, methylene blue, and methyl orange with a rate constant(k) of 0.038, 0.011, and 0.007 min–1 respectively, using H2O2. This fast and simplemethod could help to develop a new pathway for differently shapedoxide nanoparticles in a sustainable and economical manner that canbe harnessed as nanozymes for industrial as well as biological applications.
机译:纳米酶是具有固有酶学性质的纳米材料,其发展已成为天然酶的诱人替代品,具有从化学工业到生物医学的巨大应用潜力。具有受控非球形形状的微米级氧化物材料的自组装生长可能是增强作为人造酶活性的重要工具,因为这些超结构的形成通常会导致高表面积,并对催化活性产生有利影响。在本文中,报道了通过单锅微波法并使用水-聚乙二醇混合物作为溶剂而生长的棒状Fe3O4微观结构,而没有涉及外部形状定向剂。前体金属盐在氧化铁微/纳米材料的尺寸,形状和相选择演化中起关键作用。尽管使用Fe(NO3)3作为金属盐前驱体获得了自组装的微棒超结构,但使用FeCl3或乙酸铁作为前驱体分别提供了中空的Fe2O3微粒和Fe3O4纳米颗粒。石墨层沉积在Fe3O4表面,由于聚乙二醇的高温处理而产生负表面电荷。棒状Fe3O4微晶显示出有效的过氧化物酶模拟对3,3,5,5'-四甲基联苯胺和邻苯三酚的活性作为过氧化物酶底物,具有Michaelis–Menten速率常数(Km)值分别为0.05和0.52 mM。这些磁性超结构的熟练酶模拟行为进一步探索了降解有机染料的方法,包括罗丹明B,亚甲基蓝和甲基橙,速率常数(k)使用H2O2分别为0.038、0.011和0.007 min –1 。这样快速简单方法可以帮助开发出不同形状的新途径以可持续和经济的方式氧化纳米颗粒可作为工业和生物学应用的纳米酶。

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