Composted organic biomasses at 60, 90, and 150 days of maturity were studied for changes inmolecular
composition. Compost samples were subjected to a mild sequential fractionation basedon (1) organic solvent extraction, (2) transesterification with boron trifluoride in methanol (BF
3-CH
3OH), and (3) methanolic alkaline hydrolysis (KOH-CH
3OH). The general chemical variations in
compost residues following fractionation were monitored by DRIFT spectroscopy, whereas themolecular
components separated along the fractionation steps were identified by GC-MS. DRIFTspectra suggested a progressive decrease of
biolabile
compounds such as alkyls, carbohydrates,and proteinaceous materials with
compost maturity. Extraction of unbound
components in an organicsolvent indicated a considerable reduction of linear and branched alkanoic acids, both saturated andunsaturated,
n-alkanes, and
n-alkanols with enhancing
compost maturity. Extracts of weakly boundmolecules by transesterification revealed a decrease, with
compost maturity, of
components frommore recalcitrant plant polyesters, such as
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-, di-, and trihydroxy acids, dioic acids, and
n-alkanols.Extracts of strongly bound molecules by alkaline hydrolysis indicated a lower decrease of the same
components, suggesting their reduced availability when in stable hydrophobic domains of progressivelymature
compost. The largest decrease in molecular
components occurred when
compost wasstabilized from 60 to 90 days, whereas its
composition did not significantly vary after stabilization at150 days. The molecular structures of a number of steroids and terpenes appeared to be lesssusceptible to transformation with
composting maturity, thereby resulting as useful biomarkers totrace the fate of
composted organic matter in the environment. This work showed that a detailedmolecular characterization of
compost by a stepwise chemical fractionation enables the evaluationof
compost maturity and origin of
composted biomasses, as well as the identification of environmentaltracers.