1990
DOI: 10.1002/j.1551-8833.1990.tb07022.x
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Pyrolysis–GC–MS for Investigating High‐Molecular‐Weight THM Precursors and Other Refractory Organics

Abstract: Specific problems encountered during water treatment are known to be a function of the type of macromolecules present. The pyrolysis–GC–MS analytical technique described in this article shows the inadequacy of existing models to accurately reflect the complex mixture that comprises the organic matrix of natural waters. In fact, the highly condensed aromatic cores described by most of these models were determined by the research reported here to be minor constituents.

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Cited by 114 publications
(59 citation statements)
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“…The peak areas of select pyrochromatogram byproducts can also be used to estimate the relative proportion of the major biopolymers in the original organic matrix (32). The variability of the biopolymer distribution of NOM fractions determined by the pyrolysis approach agreed with the structural differences inferred from other analytical techniques, such as 13 C NMR, elemental analysis, and specific component analyses.…”
Section: Range Ofmentioning
confidence: 52%
“…The peak areas of select pyrochromatogram byproducts can also be used to estimate the relative proportion of the major biopolymers in the original organic matrix (32). The variability of the biopolymer distribution of NOM fractions determined by the pyrolysis approach agreed with the structural differences inferred from other analytical techniques, such as 13 C NMR, elemental analysis, and specific component analyses.…”
Section: Range Ofmentioning
confidence: 52%
“…The information gained from TMAH-Py-GC/MS analyses is only semi-quantitative; for example, although the sample is almost entirely burned during the pyrolysis process, significant amounts of carbon are transformed into small molecules such as HCN, CO 2 , and CH 4 which are difficult to quantify (Bruchet et al 1990). Additionally, it is important to consider that TMAH-Py-GC/MS produces the methyl esters of carboxylic acids and methyl ether of alcohols (Challinor 1989).…”
Section: Peat and Litter Characterizationmentioning
confidence: 99%
“…The temperature program of the GC oven was initially maintained at 40 • C for 5 min, then increased at 7 • C min −1 to a final temperature of 300 • C and remained there for 10 min, giving a total run time of 52.14 min. The interpretation of the pyrochromatograms was conducted according to the methods described in Bruchet et al (1990).…”
Section: Sample Collection and Analysismentioning
confidence: 99%