ANALYSIS OF DRINKING-WATER FOR TRACE ORGANICS

被引:67
作者
KOESTER, CJ [1 ]
CLEMENT, RE [1 ]
机构
[1] ONTARIO MINIST ENVIRONM & ENERGY, SERV BRANCH LAB, 125 RESOURCES RD, ETOBICOKE M9P 3V6, ON, CANADA
关键词
DRINKING WATER; TRACE ORGANICS; GAS-CHROMATOGRAPHY MASS-SPECTROMETRY (GC-MS); LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY (LC-MS); SAMPLING; SAMPLE PREPARATION; PURGE AND TRAP (P-AND-T); HEADSPACE ANALYSIS; SOLID-PHASE EXTRACTION (SPE); VOLATILE ORGANIC COMPOUNDS (VOCS); SEMIVOLATILE ORGANIC COMPOUNDS (SVOCS); POLAR ORGANIC COMPOUNDS; CHLORINATED DIBENZO-P-DIOXINS (PCDDS);
D O I
10.1080/10408349308050555
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The protection of drinking water quality is one of the most important mandates of government environment departments. During the past 2 decades, more and more attention has been spent on the trace organic chemical pollutants that may be present in potable water. Consequently, the detection, identification, and quantitation of trace organics in drinking water has been the subject of considerable analytical development work. Sophisticated methods based on gas chromatography-mass spectrometry (GC-MS) are now in routine use that can detect organics at parts per trillion concentrations. For some analytes, parts per quadrillion detection limits have been reported. Although these capabilities are largely due to the maturity of GC-MS as an analytical technique, recent developments in solid-phase extraction (SPE) and other reduced-solvent or even solvent-free extraction and concentration methods are leading the way to even greater analytical performance. Other methods based on liquid chromatography-mass spectrometry (LC-MS) may lead to concern over many other analytes not determined by GC-MS. The above and related techniques are reviewed to demonstrate the state of current analytical methods for the determination of trace organics in drinking water samples, and to discuss future developments. Throughout the 1980s, development of GC-MS instrumentation and chromatographic procedures were paramount, but attention has now shifted to improving sample preparation methods. Eventually, the development of fully automated methods from sampling to report generation will be realized.
引用
收藏
页码:263 / 316
页数:54
相关论文
共 199 条
  • [1] APPLICATION OF GAS-CHROMATOGRAPHY MASS-SPECTROMETRY FOR RAPID DETECTION OF MYCOBACTERIUM-XENOPI IN DRINKING-WATER
    ALUGUPALLI, S
    LARSSON, L
    SLOSAREK, M
    JARESOVA, M
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (11) : 3538 - 3541
  • [2] [Anonymous], 1989, J CHROMATOGRAPHY LIB
  • [3] QUANTITATION AND LINEARITY FOR PARTICLE-BEAM LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY
    APFFEL, A
    PERRY, ML
    [J]. JOURNAL OF CHROMATOGRAPHY, 1991, 554 (1-2): : 103 - 118
  • [4] ARTHUR CL, 1992, LC GC-MAG SEP SCI, V10, P656
  • [5] AUTOMATION AND OPTIMIZATION OF SOLID-PHASE MICROEXTRACTION
    ARTHUR, CL
    KILLAM, LM
    BUCHHOLZ, KD
    PAWLISZYN, J
    BERG, JR
    [J]. ANALYTICAL CHEMISTRY, 1992, 64 (17) : 1960 - 1966
  • [6] ARTHUR CL, 1992, J ENV SCI TECHNOL, V26, P979
  • [7] DETERMINATION OF TRIAZINE HERBICIDES IN SURFACE AND DRINKING WATERS BY OFF-LINE COMBINATION OF LIQUID-CHROMATOGRAPHY AND GAS-CHROMATOGRAPHY MASS-SPECTROMETRY
    BAGHERI, H
    VREULS, JJ
    GHIJSEN, RT
    BRINKMAN, UAT
    [J]. CHROMATOGRAPHIA, 1992, 34 (1-2) : 5 - 13
  • [8] BANKS JF, 1993, 41ST P ASMS C MASS S
  • [9] USE OF EXTRACTION DISKS FOR TRACE ENRICHMENT OF VARIOUS PESTICIDES FROM RIVER WATER AND SIMULATED SEAWATER SAMPLES FOLLOWED BY LIQUID-CHROMATOGRAPHY RAPID-SCANNING UV VISIBLE AND THERMOSPRAY MASS-SPECTROMETRY DETECTION
    BARCELO, D
    DURAND, G
    BOUVOT, V
    NIELEN, M
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1993, 27 (02) : 271 - 277
  • [10] DETERMINATION OF BENZENES AND NAPHTHALENES IN WATER BY PURGE AND TRAP ISOLATION AND CAPILLARY COLUMN CHROMATOGRAPHY
    BARNUNG, TN
    GRAHLNIELSEN, O
    [J]. JOURNAL OF CHROMATOGRAPHY, 1989, 466 : 271 - 278