Molecularly imprinted polymer surfaces as solid-phase extraction sorbents for the extraction of 2-nitrophenol and isomers from environmental water

被引:32
作者
Guan, Wei [1 ,2 ]
Han, Changri [1 ]
Wang, Xue [2 ]
Zou, Xiaohua [2 ]
Pan, Jianming [2 ]
Huo, Pengwei [2 ]
Li, Chunxiang [2 ]
机构
[1] Hainan Normal Univ, Coll Chem & Chem Engn, Hainan Prov Key Lab Trop Med Herb & Chem, Haikou 571158, Peoples R China
[2] Jiangsu Univ, Coll Chem & Chem Engn, Zhenjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
HPLC; Nitrophenols; Surface molecularly imprinted polymers; SPE; Water samples; P-NITROPHENOL; SELECTIVE RECOGNITION; LIQUID-CHROMATOGRAPHY; AQUEOUS-SOLUTION; 4-NITROPHENOL; ADSORPTION; CHLOROPHENOLS; NANOPARTICLES; DEGRADATION; COMPOSITES;
D O I
10.1002/jssc.201100768
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The novel surface molecularly imprinted polymer (MIP) with 2-nitrophenol (2-NP) as the template has been prepared and used as the adsorbent for the solid-phase extraction (SPE). The selectivity of the polymer was checked toward several selected nitrophenols (NPs) such as 2-NP, 3-nitrophenol (3-NP), 4-nitrophenol (4-NP) and 2,4,6-trichlorophenol (2,4,6-TCP). Under the optimized conditions, high sensitivity (detection limits: 0.070.12?ng/mL) and good reproducibility of analytes (2.34.8% for four cycles) were achieved. Then, the method was applied for the analysis of selected phenols in spiked tap, lake and river water samples. High recoveries (>83.3%) for nitrophenols (NPs) were obtained, but lower recoveries (<63.4%) were achieved for 2,4,6-TCP. The method was found to be linear in the range of 1300?ng/mL with correlation coefficients (R2) greater than 0.99 and repeatability relative standard deviation (RSD) below 7.2% in all cases. For analysis of 120?mL water samples, the method detection limits (LODs) ranged from 0.10 to 0.22?ng/mL and the limit of quantification (LOQs) from 0.33 to 0.72?ng/mL. These results showed the suitability of the MIP-SPE method for the selective extraction of a group of structurally related isomeric compounds.
引用
收藏
页码:490 / 497
页数:8
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