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Preparation of cyano‐functionalized multiwalled carbon nanotubes as solid‐phase extraction sorbent for preconcentration of phenolic compounds in environmental water
Author(s) -
Gao Wenhua,
Sun Ximeng,
Chen Tufeng,
Lin Yuejuan,
Chen Yaowen,
Lu Fushen,
Chen Zhanguang
Publication year - 2012
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.201200045
Subject(s) - solid phase extraction , sorbent , extraction (chemistry) , detection limit , chromatography , thermogravimetric analysis , fourier transform infrared spectroscopy , chemistry , solid phase microextraction , carbon nanotube , elution , surface modification , sample preparation , nuclear chemistry , materials science , adsorption , mass spectrometry , chemical engineering , gas chromatography–mass spectrometry , organic chemistry , nanotechnology , engineering
In the present work, we showed a novel method to synthesize cyano‐functionalized multiwalled carbon nanotubes ( MWCNTs‐CN ) and utilize it as a solid‐phase extraction sorbent for preconcentration of phenolic compounds in environmental water samples. MWCNTs‐CN was synthesized through surface functionalization of multiwalled carbon nanotubes ( MWCNT s). The functional groups on the surface of modified MWCNT s were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis and scanning electron microscopy. The analytical procedure was based on a conventional solid‐phase extraction step for which 100 mg of MWCNTs‐CN were packed in a 3 mL polypropylene cartridge. Analytes were thus isolated and preconcentrated from the pretreated samples and subsequently detected on high‐performance liquid chromatography‐ultraviolet detection. The results showed the proposed method exhibited good sensitivity and precision for the extraction and elution of analytes. The limit of detections ( S/N = 3) of the method were 0.45, 0.09, 0.08, and 3.00 ng mL −1 for p ‐chlorophenol, 1‐naphthol, 2‐naphthol, and 2,4‐dichlorophenol, respectively. The mean relative recoveries ( n = 3) were between 80.28 and 103.13%, and the repeatability ( RSD ≤ 5.10%) and reproducibility ( RSD ≤ 7.68%) were accepted. This developed method was applied to determine phenolic compounds in environmental water samples. There is a positive result only for 2‐naphthol with concentration of 0.38 ng mL −1 in seawater sample.
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