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    Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/100199


    Title: Determination of synthetic polycyclic musks in aqueous samples by ultrasound-assisted dispersive liquid-liquid microextraction and gas chromatography-mass spectrometry
    Authors: 丁望賢;Yang, Ching-Ya;Ding, Wang-Hsien
    Contributors: 理學院化學學系
    Keywords: Analysis;Analytical Chemistry;Biochemistry;Carbon tetrachloride;Characterization and Evaluation of Materials;Chemistry;Chemistry and Materials Science;Extraction;Fatty Acids, Monounsaturated - analysis;Fatty Acids, Monounsaturated - isolation & purification;Food Science;Gas chromatography;Gas Chromatography-Mass Spectrometry - methods;Laboratory Medicine;Liquid Phase Microextraction - methods;Mass spectrometry;Mathematical analysis;Monitoring/Environmental Analysis;Musk;Odorants - analysis;Original Paper;Sensitivity and Specificity;Spectrometry;Spectroscopy;Standard deviation;Ultrasonics - methods;Waste Disposal, Fluid;Water - analysis;Water Pollutants, Chemical - analysis;Water Pollutants, Chemical - isolation & purification
    Date: 2012-02-01
    Issue Date: 2026-04-21 13:53:23 (UTC+8)
    Publisher: Springer Verlag;Berlin/Heidelberg: Springer-Verlag
    Abstract: 摘要: A simple and solvent-minimized procedure for the determination of six commonly found synthetic polycyclic musks in aqueous samples using ultrasound-assisted dispersive liquid–liquid microextraction (UA-DLLME) coupled with gas chromatography–mass spectrometry (GC-MS) is described. The parameters affecting the extraction efficiency of analytes from water samples were systematically investigated. The best extraction conditions involved the rapid injection of a mixture of 1.0 mL of isopropyl alcohol (as a dispersant) and 10 μL of carbon tetrachloride (as an extractant) into 10 mL of water containing 0.5 g of sodium chloride in a conical-bottom glass tube. After ultrasonication for 1.0 min and centrifugation at 5,000 rpm (10 min), the sedimented phase 1.0 μL was directly injected into the GC-MS system. The limits of quantitation (LOQs) were less than 0.6 ng/L. The precision for these analytes, as indicated by relative standard deviations (RSDs), was less than 11% for both intra- and interday analysis. Accuracy, expressed as the mean extraction recovery, was between 71 and 104%. Their total concentrations were determined in the range from 8.3 to 63.9 ng/L in various environmental samples by using a standard addition method.
    其他題名: Anal Bioanal Chem
    出版者: Berlin/Heidelberg: Springer-Verlag
    出版日期: 2012-02
    出處: Analytical and bioanalytical chemistry, 2012-02, Vol.402 (4), p.1723-1730
    資源來源: EBSCOhost Academic Search Premier
    版權: Springer-Verlag 2011
    版權: COPYRIGHT 2012 Springer
    識別號: ISSN: 1618-2642
    識別號: ISSN: 1618-2650
    識別號: EISSN: 1618-2650
    識別號: DOI: 10.1007/s00216-011-5573-3
    識別號: PMID: 22139524
    Appears in Collections:[Department of Chemistry] journal & Dissertation

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