衍生后分光光度法测定氮嘧菌酯杀菌剂含量的研究

Kafeel Khan, H. Gulab, Farzana Hai̇der
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引用次数: 1

摘要

建立了一种紫外可见分光光度法测定杀菌剂偶氮嘧菌酯的方法。偶氮杀菌剂在盐酸羟胺存在下,与氯化铁(III)在碱性介质中进行络合反应,得到红褐色络合物。用紫外可见分光光度计在513 nm处测定了配合物的吸光度。对影响衍生化反应的不同参数进行了研究和优化。在1 ~ 12 μg mL-1浓度范围内符合比尔定律。计算其摩尔吸光度、检出限和定量限分别为4.3 × 10-4 L mol-1 cm-1、0.38 μg mL-1和1.26 μg mL-1。同样计算残留测定的平均检出限和定量限,分别为3.8±1.02 μg mL-1和3.98±1.4 μg mL-1。该方法成功地应用于偶氮嘧菌酯的纯态和商业配方的测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Spectrophotometric Method for the Determination of Azoxystrobin Fungicide after Derivatization
A UV-Visible spectrophotometric method has been developed for the determination of azoxystrobin fungicide. Complexation reaction of the azoxystrobin fungicide was carried out with the Ferric (III) chloride in presence of hydroxylamine hydrochloride in alkaline medium resulting in a reddish-brown color complex. The absorbance of the complex was measured at 513 nm using UV-visible spectrophotometer. Different parameters affecting the derivatization reactions were carefully studied and optimized. Beer’s law was obeyed in the concentration range of 1-12 μg mL-1. The molar absorptivity, limit of detection and limit of quantification were calculated and found to be 4.3 × 10-4 L mol-1 cm-1, 0.38 μg mL-1 and 1.26 μg mL-1 respectively. Similarly, the mean limit of detection and limit of quantification were calculated for residue determination and were found to be 3.8 ± 1.02 μg mL-1 and 3.98 ± 1.4 μg mL-1, respectively. The proposed method was successfully applied for the determination of azoxystrobin in pure form and in commercial formulations.
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