Enantioselective separation and degradation of the herbicide dichlorprop methyl in sediment.

Abstract:

:Chiral pesticides currently constitute about 50% of all pesticides dosage used in China, and this ratio is increasing as more complex structures are introduced. Dichlorprop methyl (DCPPM) is a chiral herbicide consisting of a pair of enantiomers. In this study, the enantiomeric separation of DCPPM was investigated by gas chromatography (GC) and high-performance liquid chromatography (HPLC) using chiral stationary phases (CSPs), and its enantiomeric degradation was characterized using a DCPPM-degrading bacterial strain isolated from an activated sludge from a textile-printing wastewater treatment plant. Baseline separation by both GC and HPLC was achieved. Incubation with DCPPM-degrading bacteria in different pH solutions showed that the R enantiomer was preferentially degraded over the S enantiomer of DCPPM. The degradation rate constant decreased with increasing pH in the order of k(pH5) approximately k(pH7) >k(pH9). In comparison, the enantioselectivity as indicated by EF followed the order of pH 7 > pH 9-pH 5.

journal_name

Chirality

journal_title

Chirality

authors

Ma Y,Xu C,Wen Y,Liu W

doi

10.1002/chir.20624

subject

Has Abstract

pub_date

2009-04-01 00:00:00

pages

480-3

issue

4

eissn

0899-0042

issn

1520-636X

journal_volume

21

pub_type

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