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In situ hydrothermal growth of a dual-ligand metal-organic framework film on a stainless steel fiber for solid-phase microextraction of polycyclic aromatic hydrocarbons in environmental water samples
被引:58
|作者:
Huo, Shu-Hui
[1
]
Yu, Jing
[1
]
Fu, Yan-Yan
[2
]
Zhou, Peng-Xin
[1
]
机构:
[1] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Ecoenvironm Related Polymer Mat, Minist Educ, Lanzhou 730070, Peoples R China
[2] Tianjin Med Univ, Sch Med Imaging, Tianjin 300203, Peoples R China
来源:
RSC ADVANCES
|
2016年
/
6卷
/
17期
基金:
中国国家自然科学基金;
中国博士后科学基金;
关键词:
LIQUID-CHROMATOGRAPHIC SEPARATION;
ZEOLITIC IMIDAZOLATE FRAMEWORK-8;
TANDEM MASS-SPECTROMETRY;
POLYCHLORINATED-BIPHENYLS;
MIL-101(CR);
FABRICATION;
EXTRACTION;
POLYMER;
ADSORPTION;
CAPILLARY;
D O I:
10.1039/c5ra26656d
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Effective enrichment and determination of polycyclic aromatic hydrocarbons (PAHs) in environmental aqueous solutions is still a major challenge because of their poor solubility and low concentration in the environmental matrix. Solid-phase microextraction (SPME) has been proven to be an effective technique for analyzing trace analytes from environmental samples. Herein, we report the fabrication of a dualligand metal-organic framework (MOF) bio-MOF-1-coated stainless steel fiber via an in situ growth approach for SPME of six PAHs in water samples. Such MOF-based SPME in combination with gas chromatography (GC) gave enhancement factors of 3104-5980, ranges of 10-100 mu g L-1 for Nap, Ace, and Fle, 2.5-100 mu g L-1 for Phen, 0.1-100 mu g L-1 for FluA and Pyr, detection limits (S/N = 3) of 0.02-5.57 mg L-1, and quantitation limits (S/N = 10) of 0.14-17.2 mu g L-1 for the studied PAHs. The recoveries obtained by spiking 10 mu g L-1 PAHs in water samples ranged from 80% to 115%. The results showed that p-p interaction with biphenyldicarboxylate and pi-complexation between aromatic rings and the pyrimidine in the pores of bio-MOF-1 play significant roles in the extraction of PAHs.
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页码:14042 / 14048
页数:7
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