1980
DOI: 10.1021/es60168a002
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Determining volatile organics in water

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1983
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Cited by 18 publications
(6 citation statements)
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“…Activated charcoal was not evaluated due to its reported irreversible binding to various organic compounds (Mieure, 1980 Calibration was achieved by exposing all eight devices for times between four and twenty-four hours and concentrations from 0.01 to 0.3 mg/L (Table 3) Initial calibration of each device can be used to account for any device to device variation by use of their individual permeation constants (K). mg/L and times ranged from 4 to 24 hours.…”
Section: Resultsmentioning
confidence: 99%
“…Activated charcoal was not evaluated due to its reported irreversible binding to various organic compounds (Mieure, 1980 Calibration was achieved by exposing all eight devices for times between four and twenty-four hours and concentrations from 0.01 to 0.3 mg/L (Table 3) Initial calibration of each device can be used to account for any device to device variation by use of their individual permeation constants (K). mg/L and times ranged from 4 to 24 hours.…”
Section: Resultsmentioning
confidence: 99%
“…Many analytical techniques for determining volatile halocarbons, including chloroform, in water samples have been reported (Mieure, 1980;Wolska et al, 1998;Nikolaou et al, 2002). Of those techniques, static headspace sampling by using solid-phase microextraction (SPME) is a convenient, cheaper but reliable way to isolate and concentrate many volatile halocarbons for gas-chromatographic analysis (Cai et al, 1993;Alpendurada et al, 2000).…”
Section: Discussionmentioning
confidence: 99%
“…For several decades, gas chromatography (GC) has been one of the most popular techniques for the detection, identification and separation of volatile and semi-volatile analytes, in complex, including biomass-related samples [29,30]. GC usually concentrates on the volatile organic species with lower polarity and lower boiling point (<350°C) [31].…”
Section: Gas and Liquid Chromatographymentioning
confidence: 99%