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[Study on beta-cyclodexdrin sensitizing catalytic kinetic spectrophotometric determination of Mn(II)].

Liangqia Guo, Xucong Lin, Zenghong Xie, Yan-bin Fu

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Abstract

A new catalytic spectrophotometric method for the determination of trace amount of Mn(II) has been developed. The method is based on the oxidation of alizarin green(AG) by potassium periodate in the presence of beta-cylodexdrin(beta-CD) as a sensitizer and nitrilotriacetic acid as an activator. The linear range of the method was 0-2.4 ng x mL(-1) for Mn(II), the determination limit was 0.097 ng x mL(-1), the relative standard deviation was 0.45% (n = 12) for 1.6 ng x mL(-1) of Mn(II), and the sensitivity was increased by a factor of 2.5 compared to that in the absence of the beta-CD. The method was used for the determination of Mn(II) in cereal samples and wine samples with satisfactory results. The mechanism of this reaction system was also presented.

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What this paper is about

A new catalytic spectrophotometric method for the determination of trace amount of Mn(II) has been developed. The method is based on the oxidation of alizarin green(AG) by potassium periodate in the presence of beta-cylodexdrin(beta-CD) as a sensitizer and nitrilotriacetic acid as an activator. The linear range of the method was 0-2.4 ng x mL(-1) for Mn(II), the determination limit was 0.097 ng x mL(-1), the relative standard deviation was 0.45% (n = 12) for 1.6 ng x mL(-1) of Mn(II), and the sensitivity was increased by a factor of 2.5 compared to that in the absence of the beta-CD. The method was used for the determination of Mn(II) in cereal samples and wine samples with satisfactory results. The mechanism of this reaction system was also presented.

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Available abstract

A new catalytic spectrophotometric method for the determination of trace amount of Mn(II) has been developed. The method is based on the oxidation of alizarin green(AG) by potassium periodate in the presence of beta-cylodexdrin(beta-CD) as a sensitizer and nitrilotriacetic acid as an activator. The linear range of the method was 0-2.4 ng x mL(-1) for Mn(II), the determination limit was 0.097 ng x mL(-1), the relative standard deviation was 0.45% (n = 12) for 1.6 ng x mL(-1) of Mn(II), and the sensitivity was increased by a factor of 2.5 compared to that in the absence of the beta-CD. The method was used for the determination of Mn(II) in cereal samples and wine samples with satisfactory results. The mechanism of this reaction system was also presented.

Key concepts: Potassium periodate, Nitrilotriacetic acid, Chemistry, Detection limit, Catalysis, Nuclear chemistry, Spectrophotometry, Relative standard deviation

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