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采用多通道流动注射分析法在线分光光度法测定自来水、橙汁和橙皮样品中的痕量硫脲。

An on-line spectrophotometric determination of trace amounts of thiourea in tap water, orange juice, and orange peel samples using multi-channel flow injection analysis.

作者信息

Arab Chamjangali M, Goudarzi N, Ghochani Moghadam A, Amin A H

机构信息

Department of Chemistry, Shahrood University, Shahrood, P.O. Box 36155-316, Iran.

Department of Chemistry, Shahrood University, Shahrood, P.O. Box 36155-316, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015;149:580-7. doi: 10.1016/j.saa.2015.04.110. Epub 2015 May 8.

Abstract

In this work, a flow injection analysis (FIA) method was introduced for the determination of trace amounts of thiourea in tap water. This method is based upon the inhibition effect of thiourea on the reaction between meta-cresol purple (MCP) and potassium bromate catalyzed by bromide ions in a sulfuric acid medium. In the presence of thiourea, an induction period appears in the reaction system, and as a result, the absorbance of MCP increases at 525 nm in the FIA manifold. The chemical and FIA variables are studied and optimized using the univariate and Simplex optimization methods. Under the optimum conditions, thiourea can be determined in the range of 0.100-13.0 μg mL(-1). The limit of detection (3σ) for thiourea was found to be 0.0310 μg mL(-1). The relative standard deviations (RSDs) for six replicate determinations of 0.500, 5.00, and 12.0 μg mL(-1) of thiourea were 4.0%, 1.8%, and 1.2%, respectively. The proposed method was also applied for the determination of thiourea in orange juice and orange peel samples with recoveries in the range of 98.0-101%. The analytical speed of the method was calculated to be about 120 sample per hour.

摘要

本研究介绍了一种流动注射分析(FIA)方法,用于测定自来水中痕量的硫脲。该方法基于硫脲在硫酸介质中对间甲酚紫(MCP)与溴酸钾在溴离子催化下的反应的抑制作用。在硫脲存在下,反应体系中会出现诱导期,结果在FIA流路中,MCP在525nm处的吸光度增加。采用单变量和单纯形优化方法对化学变量和FIA变量进行了研究和优化。在最佳条件下,硫脲的测定范围为0.100 - 13.0μg mL⁻¹。硫脲的检测限(3σ)为0.0310μg mL⁻¹。对0.500、5.00和12.0μg mL⁻¹硫脲进行六次重复测定的相对标准偏差(RSD)分别为4.0%、1.8%和1.2%。该方法还应用于橙汁和橙皮样品中硫脲的测定,回收率在98.0 - 101%范围内。该方法的分析速度计算约为每小时120个样品。

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