基于电位缓冲液的电位流动注射分析的氧化还原物质快速自动化分析方法。

Hiroki Ohura, Toshihiko Imato
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引用次数: 3

摘要

本文综述了基于氧化还原电位缓冲液的两种分析方法,它们证明了电位流动注射技术用于测定各种氧化还原物质的实用性。第一种是电位流注射法,其中使用氧化还原偶如Fe(III)-Fe(II), Fe(CN)(6) (3-)-Fe(CN)(CN)(6)(4-)和溴化溴和氧化还原电极或组合铂-溴离子选择电极。讨论了该方法的分析原理和优点,并给出了几个应用实例。另一个例子是高灵敏度的电位流注射法,该方法利用了氧化物质与含有溴或氯化物的Fe(III)-Fe(II)电位缓冲液反应时,由于溴或氯作为中间体而产生的大的瞬态电位变化。介绍了该方法的分析原理和细节,并给出了几种应用实例。还描述了基于检测与Ce(IV)-Ce(III)电位缓冲反应引起的瞬态电位变化的痕量肼的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rapid and automated analytical methods for redox species based on potentiometric flow injection analysis using potential buffers.

Rapid and automated analytical methods for redox species based on potentiometric flow injection analysis using potential buffers.

Rapid and automated analytical methods for redox species based on potentiometric flow injection analysis using potential buffers.

Rapid and automated analytical methods for redox species based on potentiometric flow injection analysis using potential buffers.

Two analytical methods, which prove the utility of a potentiometric flow injection technique for determining various redox species, based on the use of some redox potential buffers, are reviewed. The first is a potentiometric flow injection method in which a redox couple such as Fe(III)-Fe(II), Fe(CN)(6) (3-)-Fe(CN)(CN)(6) (4-), and bromide-bromine and a redox electrode or a combined platinum-bromide ion selective electrode are used. The analytical principle and advantages of the method are discussed, and several examples of its application are reported. Another example is a highly sensitive potentiometric flow injection method, in which a large transient potential change due to bromine or chlorine as an intermediate, generated during the reaction of the oxidative species with an Fe(III)-Fe(II) potential buffer containing bromide or chloride, is utilized. The analytical principle and details of the proposed method are described, and examples of several applications are described. The determination of trace amounts of hydrazine, based on the detection of a transient change in potential caused by the reaction with a Ce(IV)-Ce(III) potential buffer, is also described.

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