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采用 Plakett-Burman 和 Box-Behnken 设计组合优化水样中对羟基苯甲酸酯和二苯甲酮的固相萃取。

Optimization of solid-phase extraction of parabens and benzophenones in water samples using a combination of Plakett-Burman and Box-Behnken designs.

机构信息

Universidad Autónoma de Nuevo León (UANL), Facultad de Ciencias Químicas, México.

出版信息

J Sep Sci. 2018 Dec;41(24):4488-4497. doi: 10.1002/jssc.201800796. Epub 2018 Nov 21.

Abstract

An automated method for the analysis of methylparaben, propylparaben, benzophenone-3, and benzophenone-4 in water effluents via on-line solid-phase extraction coupled with high-performance liquid chromatography/ultraviolet detection was proposed. The preconcentration parameters were studied using Plackett-Burman and Box-Behnken experimental designs using a C18 sorbent material. The results demonstrated that the eluent volume, composition, and sorbent amount were statistically significant. Optimal conditions for these variables were an eluent volume of 1.55 mL, eluent composition of acetonitrile 100% v/v, and sorbent amount of 100 mg. The eluted sample was analyzed on-line using high-performance liquid chromatography equipped with a reversed-phase C18 column and ultraviolet detection. Separation of the analytes was achieved in 15 min using gradient elution with acetonitrile/water. A simple, sensitive, and rapid analytical method was proposed for personal care compounds without sophisticated or expensive equipment. The limits of detection were 1.20, 1.73, 2.51, and 4.67 μg/L for propylparaben, methylparaben, benzophenone-3, and benzophenone-4, respectively. The analysis time was 48 min, consuming only 1.59 mL of eluent acetonitrile for the solid phase extraction step, with minimal sample handling. The method was applied to the analysis of spiked swimming pool and wastewater, with recoveries between 65-107%. These results indicate the reliability of the flow-based procedure.

摘要

一种自动化方法用于分析水中的甲基对羟基苯甲酸酯、对羟基苯甲酸丙酯、二苯甲酮-3 和二苯甲酮-4,采用在线固相萃取与高效液相色谱/紫外检测相结合的方法。使用 Plackett-Burman 和 Box-Behnken 实验设计研究了预浓缩参数,使用 C18 吸附剂材料。结果表明,洗脱剂体积、组成和吸附剂用量具有统计学意义。这些变量的最佳条件为洗脱剂体积 1.55mL、洗脱剂组成 100%v/v 乙腈和吸附剂用量 100mg。洗脱后的样品在线使用高效液相色谱仪进行分析,采用反相 C18 柱和紫外检测。使用乙腈/水梯度洗脱,在 15min 内实现了分析物的分离。提出了一种简单、灵敏、快速的分析方法,用于个人护理化合物的分析,无需复杂或昂贵的设备。对羟基苯甲酸丙酯、甲基对羟基苯甲酸酯、二苯甲酮-3 和二苯甲酮-4 的检出限分别为 1.20、1.73、2.51 和 4.67μg/L。分析时间为 48min,固相萃取步骤仅消耗 1.59mL 洗脱剂乙腈,样品处理量最小。该方法应用于游泳池和废水的加标分析,回收率在 65-107%之间。这些结果表明基于流量的程序具有可靠性。

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