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.

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Tlou Auguston Makwakwa, Elsie Dineo Moema, Titus Alfred Makudali Msagati
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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-1 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-1 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.

在超高效液相色谱四极杆飞行时间质谱法测定水样中有机污染物的过程中,利用响应面法和可取函数对分散液-液微萃取因子进行方法开发和优化:风险和绿色评估。
建立并优化了一种简单、经济、高效的分散液-液微萃取方法,用于测定不同环境水基质中的有机污染物,然后进行超高效液相色谱-质谱-质谱分析。在初步实验中,采用单变量优化方法选择四氯乙烯和乙腈分别作为萃取溶剂和分散剂。利用全因子设计筛选出影响 DLLME 的重要因素,然后利用带可取函数的中心复合设计进一步优化,得出各变量的最佳值。195 μL 的四氯乙烯作为萃取溶剂,1439 μL 的乙腈作为分散溶剂,样品的 pH 值为 5.8。在这些条件下,该方法对所有样品的检出限为 0.11-0.48 μg L-1,回收率为 23.32-145.43% 。富集因子在 11.66-72.72 之间。随后,该方法被成功应用于实际水样中。在所有水样中只检测到浓度范围为 0.79-0.88 μg L-1 的二苯甲酮。计算得出的水样中接触二苯甲酮的风险商数表明,该物质对人类健康和水生生态系统的潜在风险较低。此外,还使用了多种指标工具对该方法的环保性进行了评估,如分析生态尺度(AES)、绿色分析程序指数(GAPI)、分析绿色度(AGREE)、样品制备分析绿色度(AGREEprep)和样品制备可持续性指标(SPMS)。在使用 SPMS 进行评估时,只有 AES 将该方法认定为绿色方法,而该方法被认为是可接受和可持续的。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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