An alternative clean-up column for the determination of polychlorinated biphenyls in solid matrices

被引:1
|
作者
Ndunda, Elizabeth N. [1 ]
Madadi, Vincent O. [2 ]
Mizaikoff, Boris [1 ]
机构
[1] Univ Ulm, Inst Analyt & Bioanalyt Chem, D-89081 Ulm, Germany
[2] Univ Nairobi, Dept Chem, Nairobi 30197, Kenya
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; MOLECULARLY IMPRINTED POLYMERS; PERSISTENT ORGANIC POLLUTANTS; ACCELERATED SOLVENT-EXTRACTION; POLYBROMINATED DIPHENYL ETHERS; PRESSURIZED LIQUID EXTRACTION; MICROWAVE-ASSISTED EXTRACTION; PHASE EXTRACTION; ORGANOCHLORINE PESTICIDES; SOXHLET EXTRACTION;
D O I
10.1039/c5em00409h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The need for continuous monitoring of polychlorinated biphenyls (PCBs) has necessitated the development of analytical techniques that are sensitive and selective with minimal reagent requirement. In light of this, we developed a column for clean-up of soil and sediment extracts, which is less demanding in terms of the amount of solvent and sorbent. The dual-layer column consists of acidified silica gel and molecularly imprinted polymers (MIPs). MIPs were synthesized via aqueous suspension polymerization using PCB 15 as the dummy template, 4-vinylpyridine as the functional monomer and ethylene glycol dimethacrylate as the cross-linker and the obtained particles characterized via SEM, BET, and batch rebinding assays. Pre-concentration of the spiked real-world water sample using MISPE gave recoveries between 85.2 and 104.4% (RSD < 8.69). On the other hand, the specific dual-layer column designed for clean-up of extracts from complex matrices provided recoveries of 91.6-102.5% (RSD < 4%) for spiked soil, which was comparable to clean-up using acidified silica (70.4-90.5%; RSD < 3.72%) and sulfoxide modified silica (89.7-103.0%; RSD < 13.0%). However, the polymers were reusable maintaining recoveries of 79.8-111.8% after 30 cycles of regeneration and re-use, thereby availing a cost-effective clean-up procedure for continuous monitoring of PCBs. Method detection limits were 0.01-0.08 ng g(-1) and 0.002-0.01 ng mL(-1) for solid matrices and water, respectively.
引用
收藏
页码:2101 / 2109
页数:9
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