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采用响应面法和期望函数对分散液-液微萃取因子进行方法开发和优化,用于超高效液相色谱-四极杆飞行时间质谱法测定水样中的有机污染物:风险和绿色度评估

Method development and optimization for dispersive liquid-liquid microextraction factors using the response surface methodology with desirability function for the ultra-high performance liquid chromatography quadrupole time of flight mass spectrometry determination of organic contaminants in water samples: risk and greenness assessment.

作者信息

Makwakwa Tlou Auguston, Moema Elsie Dineo, Makudali Msagati Titus Alfred

机构信息

Department of Chemistry, College of Science, Engineering and Technology, University of South Africa, Johannesburg, Florida, 1709, South Africa.

Institute for Nanotechnology and Water Sustainability, College of Science, Engineering and Technology, University of South Africa, Johannesburg, Florida, 1709, South Africa.

出版信息

Anal Methods. 2024 Nov 14;16(44):7598-7612. doi: 10.1039/d4ay01462f.

Abstract

A simple, cost effective, and efficient dispersive liquid-liquid microextraction method was developed and optimized for the determination of organic contaminants in different environmental water matrices followed by UHPLC-QTOF-MS analysis. In the preliminary experiments, the univariate optimization approach was used to select tetrachloroethylene and acetonitrile as extraction and disperser solvents, respectively. The significant factors influencing DLLME were screened using full factorial design, and the optimal values for each variable were then derived through further optimization using central composite design with desirability function. The optimal conditions were achieved with 195 μL of tetrachloroethylene as the extraction solvent, 1439 μL of acetonitrile as the disperser solvent, and a sample pH of 5.8. Under these conditions, the method provided detection limits ranging from 0.11-0.48 μg L and recoveries ranging from 23.32-145.43% across all samples. The enrichment factors obtained ranged from 11.66-72.72. The proposed method was then successfully applied in real water samples. Only benzophenone was detected in the concentration range of 0.79-0.88 μg L across all the water samples. The calculated risk quotient resulting from benzophenone exposure in water samples showed a low potential risk to human health and the aquatic ecosystem. The method was also evaluated for its environmental friendliness using various metrics tools such as Analytical Eco-Scale (AES), Green Analytical Procedure Index (GAPI), Analytical GREEnness (AGREE), Analytical Greenness for Sample Preparation (AGREEprep), and Sample Preparation Metric of Sustainability (SPMS). Only AES qualified the method as green while it was considered acceptable and sustainable when assessed using SPMS.

摘要

开发并优化了一种简单、经济高效的分散液液微萃取方法,用于测定不同环境水样中的有机污染物,随后进行超高效液相色谱-四极杆飞行时间质谱(UHPLC-QTOF-MS)分析。在初步实验中,采用单变量优化方法分别选择四氯乙烯和乙腈作为萃取溶剂和分散剂溶剂。使用全因子设计筛选影响分散液液微萃取(DLLME)的显著因素,然后通过使用具有合意函数的中心复合设计进行进一步优化,得出每个变量的最佳值。以195 μL四氯乙烯作为萃取溶剂、1439 μL乙腈作为分散剂溶剂且样品pH值为5.8时达到最佳条件。在此条件下,该方法的检测限为0.11 - 0.48 μg/L,所有样品的回收率为23.32% - 145.43%。获得的富集因子为11.66 - 72.72。所提出的方法随后成功应用于实际水样。在所有水样中仅检测到浓度范围为0.79 - 0.88 μg/L的二苯甲酮。水样中二苯甲酮暴露产生的计算风险商表明对人类健康和水生生态系统的潜在风险较低。还使用各种指标工具,如分析生态尺度(AES)、绿色分析程序指数(GAPI)、分析绿色度(AGREE)、样品制备的分析绿色度(AGREEprep)和可持续性样品制备指标(SPMS),对该方法的环境友好性进行了评估。只有AES将该方法评定为绿色,而使用SPMS评估时认为该方法是可接受和可持续的。

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