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Spectrophotometric Determination of Hydrogen Peroxide Based on Fading of Tribromoarsenazo Oxidation by Hydrogen Peroxide Catalyzed by Hemoglobin

机译:血红蛋白催化过氧化氢褪色三溴偶氮氧化褪色光度法测定过氧化氢

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摘要

In pH 3.2 CH3COOH-CH3COONa buffer solution, bovine hemoglobin (Hb) catalyzes the decolouring of oxidation tribromoarsenazo (TB-ASA) by hydrogen peroxide and between fading degree ΔA and H2O2 concentration a linear relationship exists. Based on this principle, a novel method for the determination of H2O2 has been developed. The results showed that the maximum absorption wavelength of the system is 400 nm. At this wavelength, the apparent molar absorptivity of the method is ε_(400nm) = 1.01 x 10~3 L·mol~(-1) cm~(-1) and the linear range is 4.0 x 10~(-5)-3.4 x 10~(-4) mol L~(-1) with a detection limit of 2.1 x 10~(-5) mol L~(-1). The present method has been successfully applied to the determination of H2O2 in rain waters.
机译:在pH 3.2 CH3COOH-CH3COONa缓冲溶液中,牛血红蛋白(Hb)催化过氧化氢使氧化三溴偶氮唑(TB-ASA)脱色,并且褪色度ΔA和H2O2浓度之间存在线性关系。基于此原理,开发了一种测定H2O2的新方法。结果表明,该系统的最大吸收波长为400 nm。在此波长下,该方法的表观摩尔吸收率为ε_(400nm)= 1.01 x 10〜3 L·mol〜(-1)cm〜(-1),线性范围为4.0 x 10〜(-5)-检测限为3.4 x 10〜(-4)mol L〜(-1)。本方法已成功应用于雨水中H2O2的测定。

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