吸附剂
固相微萃取
聚二甲基硅氧烷
色谱法
萃取(化学)
聚己内酯
样品制备
材料科学
纤维
膜
吸附
化学
聚合物
质谱法
气相色谱-质谱法
纳米技术
复合材料
有机化学
生物化学
作者
Łukasz Marcinkowski,Adam Kloskowski,Agata Spietelun,Jacek Namieśnik
标识
DOI:10.1007/s00216-014-8328-0
摘要
Commercially available solid-phase microextraction fibers used for isolation of polar analytes are based on the adsorption phenomenon. In consequence, typical limitations bonded with analytes displacement and matrix effects are very frequent. In the present study, alternative solution is described. Polycaprolactone (PCL) was used for the first time as sorbent to isolate polar organic compounds from water samples using the membrane-solid-phase microextraction (M-SPME) technique. In this technique, due to protective role of the mechanically and thermally stable polydimethylsiloxane (PDMS) membrane, internal polar coating might be melted during extraction and desorption of analytes. In consequence sorbents with low melting points like a PCL might be utilized. Based on chromatographic retention data, triazines were selected as a model compounds for evaluation of the sorptive properties of the polycaprolactone. Applying the screening plan and central composite design, statistically significant parameters influencing extraction efficiency were determined and optimized. The analysis of variance confirmed the significant influence of temperature, salt content, and pH of samples on the extraction efficiency. Besides the new PCL/PDMS fiber, a commercial fiber coated with divinylbenzene/polydimethylsiloxane (DVB/PDMS) was used for comparative studies. The results obtained showed that PCL is an interesting sorbent which can be successfully applied for isolation of polar organics from aqueous matrices at a broad range of analytes concentration. The determined detection limits of procedure based on the novel fiber enable its application at the concentration levels of triazines recommended by the US EPA standards. The practical applicability of the developed fiber has been confirmed by the results based on the analysis of real samples.
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