4.6 Article

Development, optimisation and application of polyurethane foams as new polymeric phases for stir bar sorptive extraction

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JOURNAL OF CHROMATOGRAPHY A
卷 1171, 期 1-2, 页码 8-14

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ELSEVIER
DOI: 10.1016/j.chroma.2007.09.033

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stir bar sorptive extraction; polymeric phases; polyurethane foams; adsorbents; HPLC-DAD; LVI-GC-MS; water analysis; atrazine; 2,3,4,5-tetrachlorophenol; fluorene

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In this contribution, polyurethane foams are proposed as new polymeric phases for stir bar sorptive extraction (SBSE). Assays performed for polyurethane synthesis demonstrated that four series of formulations (P-1, P-2, P-3 and P-4) present remarkable stability and excellent mechanical resistance to organic solvents. For polymer clean-up treatment, acetonitrile proved to be the best solvent under sonification, ensuring the reduction of the contamination and interferences. SBSE assays performed on these polyurethane polymers followed by liquid desorption and high-performance liquid chromatography-diode array detection (LD-HPLC-DAD) or large volume injection-capillary gas chromatography-mass spectrometry (LD-LVI-GC-MS), showed that P2 Presents the best recovery yields for atrazine, 2,3,4,5-tetrachlorophenol and fluorene, used as model compounds in water samples at a trace level. SBSE(P2) assays performed on this polymer mixed up with several adsorbent materials, i.e. activated carbon, a mesoporous material and a calixarene, did not bring any advantages in relation with the polymeric matrix alone. The comparison between assays performed by SBSE(P,) and by the conventional SBSE(PDMS) showed much better performance for the former phase on aqueous samples spiked with atrazine, 2,3,4,5-tetrachlorophenol and fluorene, in which the foremost two analytes present recovery values 3- and 10-fold higher, respectively. The polyurethanes proposed as new polymeric phases for SBSE provided powerful capabilities for the enrichment of organic compounds from aqueous matrices, showing to be indicated mainly in the case of the more polar analytes. (c) 2007 Elsevier B.V. All rights reserved,

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