کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5131038 1490861 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Magnetic headspace adsorptive extraction of chlorobenzenes prior to thermal desorption gas chromatography-mass spectrometry
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Magnetic headspace adsorptive extraction of chlorobenzenes prior to thermal desorption gas chromatography-mass spectrometry
چکیده انگلیسی


- A new extraction technique named Magnetic Headspace Adsorptive Extraction is presented.
- Graphene oxide/iron oxide composite deposited on a neodymiun magnet as sorbent.
- Sorbent of low cost, rapid and simple synthesis, easy manipulation and portability options.
- Fast and efficient extraction and sensitive determination of chlorobenzenes in water samples.

This study presents a new, user-friendly, cost-effective and portable headspace solid-phase extraction technique based on graphene oxide decorated with iron oxide magnetic nanoparticles as sorbent, located on one end of a small neodymium magnet. Hence, the new headspace solid-phase extraction technique has been called Magnetic Headspace Adsorptive Extraction (Mag-HSAE). In order to assess Mag-HSAE technique applicability to model analytes, some chlorobenzenes were extracted from water samples prior to gas chromatography-mass spectrometry determination. A multivariate approach was employed to optimize the experimental parameters affecting Mag-HSAE. The method was evaluated under optimized extraction conditions (i.e., sample volume, 20 mL; extraction time, 30 min; sorbent amount, 10 mg; stirring speed, 1500 rpm, and ionic strength, non-significant), obtaining a linear response from 0.5 to 100 ng L−1 for 1,3-DCB, 1,4-DCB, 1,2-DCB, 1,3,5-TCB, 1,2,4-TCB and 1,2,3-TCB; from 0.5 to 75 ng L−1 for 1,2,4,5-TeCB, and PeCB; and from 1 to 75 ng L−1 for 1,2,3,4-TeCB. The repeatability of the proposed method was evaluated at 10 ng L−1 and 50 ng L−1 spiking levels, and coefficients of variation ranged between 1.5 and 9.5% (n = 5). Limits of detection values were found between 93 and 301 pg L−1. Finally, tap, mineral and effluent water were selected as real water samples to assess method applicability. Relative recoveries varied between 86 and 110% showing negligible matrix effects.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Analytica Chimica Acta - Volume 971, 8 June 2017, Pages 40-47
نویسندگان
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