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首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Electrochemistry and electrocatalysis of hemoglobin in nafionano-CaCO3 film on a new ionic liquid BPPF6 modified carbon paste electrode
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Electrochemistry and electrocatalysis of hemoglobin in nafionano-CaCO3 film on a new ionic liquid BPPF6 modified carbon paste electrode

机译:新型离子液体BPPF6修饰碳糊电极上nafion / nano-CaCO3膜中血红蛋白的电化学和电催化

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摘要

Room temperature ionic liquid N-butylpyridinium hexafluorophosphate (BPPF6) was used as a binder to construct a new carbon ionic liquid electrode (CILE), which exhibited enhanced electrochemical behavior as compared with the traditional carbon paste electrode with paraffin. By using the CILE as the basal electrode, hemoglobin (Hb) was immobilized on the surface of the CILE with nano-CaCO3 and Nafion film step by step. The Hb molecule in the film kept its native structure and showed good electrochemical behavior. In pH 7.0 Britton-Robinson (B-R) buffer solution, a pair of well-defined, quasi-reversible cyclic voltammetric peaks appeared with cathodic and anodic peak potentials located at -0.444 and -0.285 V (vs SCE), respectively, and the formal potential (E degrees') was at -0.365 V, which was the characteristic of Hb Fe(III)/Fe(II) redox couples. The formal potential of Hb shifted linearly to the increase of buffer pH with a slope of -50.6 mV pH(-1), indicating that one electron transferred was accompanied with one proton transportation. Ultraviolet-visible (UV-vis) and Fourier transform infrared (FT-IR) spectroscopy studies showed that Hb immobilized in the Nafionano-CaCO3 film still remained its native arrangement. The Hb modified electrode showed an excellent electrocatalytic behavior to the reduction of H2O2, trichloroacetic acid (TCA), and NaNO2.
机译:室温离子液体六氟磷酸正丁基吡啶鎓(BPPF6)作为粘合剂来构建新型碳离子液体电极(CILE),与传统的石蜡碳糊电极相比,电化学行为增强。通过使用CILE作为基底电极,逐步将血红蛋白(Hb)固定在具有纳米CaCO 3和Nafion膜的CILE表面上。膜中的Hb分子保持其天然结构并显示出良好的电化学行为。在pH 7.0的Britton-Robinson(BR)缓冲溶液中,出现了一对明确定义的,准可逆的循环伏安峰,其阴极和阳极峰电位分别位于-0.444和-0.285 V(vs SCE)上,并且形式上电位(E度)为-0.365 V,这是Hb Fe(III)/ Fe(II)氧化还原对的特征。 Hb的形式势随缓冲液pH的增加线性变化,斜率为-50.6 mV pH(-1),表明一个电子转移伴随着一个质子迁移。紫外可见(UV-vis)和傅立叶变换红外(FT-IR)光谱研究表明,固定在Nafion / nano-CaCO3膜中的Hb仍然保持其天然排列。 Hb修饰电极对还原H2O2,三氯乙酸(TCA)和NaNO2表现出出色的电催化性能。

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