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采用实验设计优化多壁碳纳米管增强中空纤维固液萃取用于环境水样中多环芳烃的测定

Optimization of multiwalled carbon nanotubes reinforced hollow-fiber solid-liquid-phase microextraction for the determination of polycyclic aromatic hydrocarbons in environmental water samples using experimental design.

作者信息

Hamedi Raheleh, Hadjmohammadi Mohammad Reza

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.

出版信息

J Sep Sci. 2017 Sep;40(17):3497-3505. doi: 10.1002/jssc.201700086. Epub 2017 Aug 14.

Abstract

A novel design of hollow-fiber liquid-phase microextraction containing multiwalled carbon nanotubes as a solid sorbent, which is immobilized in the pore and lumen of hollow fiber by the sol-gel technique, was developed for the pre-concentration and determination of polycyclic aromatic hydrocarbons in environmental water samples. The proposed method utilized both solid- and liquid-phase microextraction media. Parameters that affect the extraction of polycyclic aromatic hydrocarbons were optimized in two successive steps as follows. Firstly, a methodology based on a quarter factorial design was used to choose the significant variables. Then, these significant factors were optimized utilizing central composite design. Under the optimized condition (extraction time = 25 min, amount of multiwalled carbon nanotubes = 78 mg, sample volume = 8 mL, and desorption time = 5 min), the calibration curves showed high linearity (R  = 0.99) in the range of 0.01-500 ng/mL and the limits of detection were in the range of 0.007-1.47 ng/mL. The obtained extraction recoveries for 10 ng/mL of polycyclic aromatic hydrocarbons standard solution were in the range of 85-92%. Replicating the experiment under these conditions five times gave relative standard deviations lower than 6%. Finally, the method was successfully applied for pre-concentration and determination of polycyclic aromatic hydrocarbons in environmental water samples.

摘要

开发了一种新型的中空纤维液相微萃取设计,该设计以多壁碳纳米管作为固体吸附剂,通过溶胶 - 凝胶技术将其固定在中空纤维的孔和内腔中,用于环境水样中多环芳烃的预浓缩和测定。所提出的方法同时利用了固相和液相微萃取介质。影响多环芳烃萃取的参数分两个连续步骤进行了优化,具体如下。首先,采用基于四分之一析因设计的方法来选择显著变量。然后,利用中心复合设计对这些显著因素进行优化。在优化条件下(萃取时间 = 25分钟,多壁碳纳米管用量 = 78毫克,样品体积 = 8毫升,解吸时间 = 5分钟),校准曲线在0.01 - 500纳克/毫升范围内显示出高线性(R = 0.99),检测限在0.007 - 1.47纳克/毫升范围内。对于10纳克/毫升的多环芳烃标准溶液,获得的萃取回收率在85 - 92%范围内。在这些条件下重复实验五次,相对标准偏差低于6%。最后,该方法成功应用于环境水样中多环芳烃的预浓缩和测定。

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