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采用多壁碳纳米管修饰的磁性聚酰胺-胺树枝状聚合物通过磁固相萃取法从环境水样中萃取杂环芳烃,然后用气相色谱-三重四极杆质谱法进行分析。

Magnetic solid phase extraction of heterocyclic aromatic hydrocarbons from environmental water samples with multiwalled carbon nanotube modified magnetic polyamido-amine dendrimers prior to gas chromatography-triple quadrupole mass spectrometer.

机构信息

State Key Laboratory of Heavy Oil Processing, China University of Petroleum-Beijing, Beijing 102249, China.

State Key Laboratory of Heavy Oil Processing, China University of Petroleum-Beijing, Beijing 102249, China.

出版信息

J Chromatogr A. 2021 Feb 22;1639:461921. doi: 10.1016/j.chroma.2021.461921. Epub 2021 Jan 21.

Abstract

Present study described a sensitive and efficient method for determination of heterocyclic aromatic hydrocarbons using multiwalled carbon nanotubes modified magnetic polyamido-amine dendrimers (MNPs@PAMAM-Gn@MWCNTs) as adsorbent for magnetic solid-phase extraction (MSPE) coupled with gas chromatography-triple quadrupole mass spectrometer (GC-MS/MS). Some pivotal parameters including PAMAM generation, adsorbent dosage, adsorption time, elution time and volume, pH and humic acid concentration were investigated to achieve the best adsorption efficiencies. Under the optimal conditions, 7-methylquinoline, dibenzothiophene and carbazole had good linearity in the concentration range of 0.005-20 μg L  , 9-methylcarbazole, 4-methyldibenzothiophene and 4,6-dimethyl dibenzothiophene had good linearity in the concentration range of 0.001-20 μg L  . All the correlation coefficients were higher than 0.996. The detection limits of the targets were in the range of 2.2 × 10-1.8 × 10 μg L   with precisions less than 8.28% (n = 6). The enrichment factors were in the range of 141-147. The spiked recoveries were in the range of 87.0%-115.1% (n = 3). These results indicated that the method could be a reliable alternative tool for monitoring trace heterocyclic aromatic hydrocarbons in environmental water samples.

摘要

本研究描述了一种使用多壁碳纳米管修饰的磁性聚酰胺-胺树枝状聚合物(MNPs@PAMAM-Gn@MWCNTs)作为吸附剂的用于磁性固相萃取(MSPE)与气相色谱-三重四极杆质谱(GC-MS/MS)联用的测定杂环芳烃的灵敏高效方法。研究了一些关键参数,包括 PAMAM 代、吸附剂用量、吸附时间、洗脱时间和体积、pH 值和腐殖酸浓度,以达到最佳的吸附效率。在最佳条件下,7-甲基喹啉、二苯并噻吩和咔唑在浓度为 0.005-20μg L-1 的范围内具有良好的线性关系,9-甲基咔唑、4-甲基二苯并噻吩和 4,6-二甲基二苯并噻吩在浓度为 0.001-20μg L-1 的范围内具有良好的线性关系。所有相关系数均高于 0.996。目标物的检测限在 2.2×10-1.8×10μg L-1范围内,精密度小于 8.28%(n=6)。富集因子在 141-147 范围内。加标回收率在 87.0%-115.1%(n=3)范围内。这些结果表明,该方法可作为监测环境水样中痕量杂环芳烃的可靠替代工具。

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