2007
DOI: 10.1016/j.chroma.2006.11.025
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Comparison of a variety of gas chromatographic columns with different polarities for the separation of chlorinated dibenzo-p-dioxins and dibenzofurans by high-resolution mass spectrometry

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Cited by 33 publications
(8 citation statements)
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“…For higher congeners such as TCDD, we injected 1,2,3,4-TCDD and 2,3,7,8-TCDD as shown in Fig. 7 and then used published elution order from Fishman et al and Hale et al to identify and determine the yield of the rest of the congeners [19,20]. Under oxidative conditions, OH and Cl radicals are the major carriers, favouring the formation of PCDD/F over dibenzo-p-dioxin and dibenzofuran (DD/F) by abstraction of H radicals through diketo-and etherintermediates [6,9].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…For higher congeners such as TCDD, we injected 1,2,3,4-TCDD and 2,3,7,8-TCDD as shown in Fig. 7 and then used published elution order from Fishman et al and Hale et al to identify and determine the yield of the rest of the congeners [19,20]. Under oxidative conditions, OH and Cl radicals are the major carriers, favouring the formation of PCDD/F over dibenzo-p-dioxin and dibenzofuran (DD/F) by abstraction of H radicals through diketo-and etherintermediates [6,9].…”
Section: Resultsmentioning
confidence: 99%
“…The identification of the remaining congeners was based on literature measurements of their retention order on the same column, VF-5 ms and DB-5 ms [19]. We took care in building analytical methods to allow the detection of all congeners, using additional windows defining standards.…”
Section: Yield and Distribution Of Pcdd/f As Function Of Residence Timementioning
confidence: 99%
“…The GC analyses were performed on both a DB-5MS and an SP-2331 column as described elsewhere, 18 in order to resolve all 2,3,7,8 substituted PCDD/F-congeners from each other and from non-2,3,7,8 substituted PCDD/Fs (2,3,7,8-TeCDF and 1,2,3,7,8-PeCDD partially separated). 20 To produce an easily presented overview of the results the intrinsic toxic potential of the samples (TEQ, Total Toxic Equivalent) was calculated for the PCDD/Fs by multiplying the individual concentrations with their TEF (Total Equivalency Factor) 2 and summing all contributions.…”
Section: Gc/hrms Analysismentioning
confidence: 99%
“…Ryan et al (1991), have analyzed dioxins on a variety of phases. Fishman, Martin, and Lamparski (2004), compared the 5% phenyl-methyl phases as well as with some other polar and analyte specific phases (Fishman, Martin, & Lamparski, 2007). Table 5 compares the separation of the seventeen 2,3,7,8-substituted dioxins on a variety of different phases.…”
Section: Chromatographic Separationmentioning
confidence: 99%
“…Maximum possible concentration. Reproduced with permission from Fishman, Martin, and Lamparski (2007). TABLE 6.…”
Section: Chromatographic Separationmentioning
confidence: 99%