کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5135164 1493427 2017 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Dispersive micro-solid phase extraction of aromatic amines based on an efficient sorbent made from poly(1,8-diaminonaphtalen) and magnetic multiwalled carbon nanotubes composite
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Dispersive micro-solid phase extraction of aromatic amines based on an efficient sorbent made from poly(1,8-diaminonaphtalen) and magnetic multiwalled carbon nanotubes composite
چکیده انگلیسی


- A novel magnetic multiwalled carbon nanotubes/Fe3O4@PDAN composite was synthesized.
- The sorbent was used in dispersive micro solid phase extraction of aromatic amines.
- The sorbent benefits from the excellent properties of MWCNTs, polymer and Fe3O4.
- Poly(1,8-diaminonaphtalen) layer improved the extraction efficiency of MWCNTs/Fe3O4.
- The method is simple and fast, and reduces the sorbent and solvent consumption.

In this work, the extraction of aromatic amines with an efficient magnetic multiwalled carbon nanotubes/Fe3O4@Poly(1,8-diaminonaphtalen) (MWCNTs/Fe3O4@PDAN) composite followed by HPLC-DAD was presented. Imprimis, the comparison among different magnetic nanosorbents including Fe3O4, MWCNTs/Fe3O4, Fe3O4@PDAN and MWCNTs/Fe3O4@PDAN was conducted. The obtained results, exhibited that the MWCNTs/Fe3O4@PDAN composite has the highest extraction efficiency for target analytes (3-nitroaniline, 4-chloroaniline, 4-bromoaniline and 3,4-dichloroaniline). This sorbent was characterized by Fourier transform infrared spectroscopy, X-ray dispersive spectroscopy, thermogravimetry analysis, scanning electron microscopy, transition electron microscopy, vibrating sample magnetometry and X-ray diffraction. Design of experiment approach was applied to find out the optimal experimental conditions. The optimal extraction conditions were: pH of the sample, 10; sorbent amount, 10 mg; sorption time, 15 min; salt concentration, 10% w/w; type and volume of the eluent, 0.01 mol L−1 HCl in acetonitrile, 145 μL; elution time; 2 min. Under the optimal extraction conditions detection limits and linear dynamic ranges were achieved in the range of 0.1-0.25 μg L−1 and 0.25-500 μg L−1, respectively. The percent of extraction recovery and relative standard deviations (n = 5) were in the range of 31.2-82.8% and 3.4-5.6%, respectively. Finally, the applicability of the method was successfully confirmed by the extraction and determination of target analytes in various water samples.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1499, 26 May 2017, Pages 38-47
نویسندگان
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