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采用氧化石墨烯/Fe<sub>3</sub>O<sub>4</sub>纳米复合材料作为固相萃取吸附剂,通过 GC-MS 法测定水样中的硅氧烷。

Determination of siloxanes in water samples employing graphene oxide/Fe O nanocomposite as sorbent for magnetic solid-phase extraction prior to GC-MS.

机构信息

Departamento de Química Analítica, Nutrición y Bromatología e Instituto Universitario de Materiales, Universidad de Alicante, Alicante, Spain.

CAPES Foundation, Ministry of Education of Brazil, Brasília, DF, Brazil.

出版信息

J Sep Sci. 2018 Nov;41(22):4177-4184. doi: 10.1002/jssc.201800577. Epub 2018 Oct 10.

Abstract

A new, fast, simple, and environmentally friendly analytical method has been developed to determine six siloxanes in water samples: octamethyltrisiloxane, octamethylcyclotetrasiloxane, decamethyltetrasiloxane, decamethylcyclopentasiloxane, dodecamethylpentasiloxane and dodecamethylcyclohexasiloxane. The analytical method consists of magnetic solid-phase extraction employing graphene oxide/Fe O as sorbent for the separation and preconcentration of siloxanes prior to GC-MS determination. The extraction procedure was optimized by means of a Plackett-Burman design. Under the optimized extraction conditions (graphene oxide/Fe O , 20 mg; extraction time, 10 min; eluent volume, 0.5 mL ACN; elution time, 2.5 min; sample volume, 20 mL), the method rendered repeatability levels with a relative standard deviation between 9 and 20% (n = 6, 10 μg/L). Methodological limits of detection ranged from 0.003 to 0.1 μg/L. The linearity of the method was studied between the methodological limit of quantification and 100 μg/L, obtaining correlation coefficient values between 0.990 and 0.999. The applicability of the method was assessed by analyzing drinking, river and wastewater samples. Relative recovery values ranged between 70 and 120% (1 and 60 μg/L spiking level) showing that the matrix had a negligible effect on extraction. Finally, the greenness of this method was confirmed by the semiquantitative Eco-Scale metrics.

摘要

一种新的、快速、简单且环保的分析方法已经被开发出来,用于测定水样中的六种硅氧烷:八甲基环四硅氧烷、八甲基三硅氧烷、十甲基四硅氧烷、十甲基环五硅氧烷、十二甲基六硅氧烷和十二甲基环己硅氧烷。该分析方法包括使用氧化石墨烯/Fe O 作为吸附剂的磁固相萃取,用于分离和浓缩硅氧烷,然后进行 GC-MS 测定。通过 Plackett-Burman 设计对萃取程序进行了优化。在优化的萃取条件下(氧化石墨烯/Fe O ,20 mg;萃取时间,10 min;洗脱体积,0.5 mL ACN;洗脱时间,2.5 min;样品体积,20 mL),该方法的重复性水平在 9%至 20%之间(n=6,10 μg/L)。方法检出限范围为 0.003 至 0.1 μg/L。该方法的线性范围在方法定量限和 100 μg/L 之间进行了研究,得到的相关系数值在 0.990 至 0.999 之间。通过分析饮用水、河水和废水样本来评估方法的适用性。相对回收率在 70%至 120%之间(1 和 60 μg/L 加标水平),表明基质对萃取的影响可以忽略不计。最后,通过半定量生态尺度指标证实了该方法的绿色性。

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