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FERROCENE-CONJUGATED POLYANILINE-MODIFIED ENZYME ELECTRODES FOR DETERMINATION OF PEROXIDES IN ORGANIC MEDIA

机译:二茂铁偶联的聚苯胺修饰的酶法测定有机介质中的过氧化物

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The development and characteristics of a reagentless amperometric organic phase enzyme electrode (OPEE) employing covalently attached horseradish peroxidase and an electrochemically deposited ferrocene-modified polyaniline film on a glassy carbon electrode is reported, The covalent attachment of ferrocene to an electrochemically deposited insoluble polymer film provided a mechanism of preventing the leaching of ferrocene into the predominantly organic solvents, required for construction of reagentless OPEE. Hydrodynamic voltammetry studies showed that the response of the OPEE to hydrogen peroxides increased at higher cathodic potentials; however, interference due to molecular oxygen also increased. Interference of molecular oxygen was minimized when the OPEE was operated at an applied potential of -50 mV (or less negative) vs Ag/AgCl. The cathodic response of the OPEE was found to increase steeply when the aqueous buffer content of the acetonitrile was increased from 0% to 5% and then plateau with no further increase when the buffer content was increased to 30%. The dynamic properties of this enzyme electrode were exploited for the detection of micromolar concentrations of different peroxides in now injection analysis where the sensitivity trend was lauroyl peroxide > hydrogen peroxide > 2-butanone peroxide > cumene hydroperoxide > tert-butyl hydroperoxide. Applicability of the enzyme electrode for measurement of peroxide in real sample was demonstrated.
机译:报告了在玻璃碳电极上使用共价连接的辣根过氧化物酶和电化学沉积的二茂铁改性的聚苯胺膜的无试剂安培有机相酶电极(OPEE)的开发和特性。一种防止二茂铁浸出到有机溶剂中的机制,这是构建无试剂OPEE所必需的。流体动力学伏安法研究表明,在较高的阴极电势下,OPEE对过氧化氢的反应增加。但是,由于分子氧的干扰也增加了。当OPEE在相对于Ag / AgCl的-50 mV(或更小的负电势)施加电势下运行时,分子氧的干扰被最小化。当乙腈的含水缓冲液含量从0%增加到5%时,发现OPEE的阴极响应急剧增加,然后当缓冲液含量增加到30%时,平台反应不再平稳。在现在的进样分析中,利用该酶电极的动态特性检测不同过氧化物的微摩尔浓度,其灵敏度趋势为月桂酰过氧化物>过氧化氢> 2-丁酮过氧化物>枯烯过氧化氢>叔丁基过氧化氢。证明了酶电极在实际样品中测量过氧化物的适用性。

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