TRANSFORMATION KINETICS AND PATHWAYS OF CHLOROPHENOLS AND HEXACHLOROBENZENE IN FRESH-WATER LAKE SEDIMENT UNDER ANAEROBIC CONDITIONS

Citation
S. Susarla et al., TRANSFORMATION KINETICS AND PATHWAYS OF CHLOROPHENOLS AND HEXACHLOROBENZENE IN FRESH-WATER LAKE SEDIMENT UNDER ANAEROBIC CONDITIONS, Environmental technology, 18(9), 1997, pp. 903-911
Citations number
36
Categorie Soggetti
Environmental Sciences
Journal title
ISSN journal
09593330
Volume
18
Issue
9
Year of publication
1997
Pages
903 - 911
Database
ISI
SICI code
0959-3330(1997)18:9<903:TKAPOC>2.0.ZU;2-V
Abstract
The anaerobic transformation of chlorophenols (CPs) and hexachlorobenz ene (HCB) was examined in a fresh water lake sediment collected from L ake Kasumigaura in Japan. Anaerobic experiments were carried out by sp iking each compound in a number of test tubes and the change in parent compound concentration was monitored for a year. Lag periods of 1-31 days were observed for the substrates examined. The first-order rate c onstants determined following the lag period, ranged between 0.0021 an d 0.072 day(-1) for chlorophenols and 0.011 day(-1) for hexachlorobenz ene. Two pathways for pentachlorophenol (PCP) in the sediment were obs erved: in the first one, under sulfidogenic conditions, PCP transforme d to 3-chlorophenol (3-CP) as, 2,3,5,6-tetrachlorophenol (2,3,5,6-TeCP ), 2,3,5-trichlorophenol (2,3,5-TCP), 3,5-dichlorophenol (3,5-DCP), 3- CP; and in the second pathway, under methanogenic conditions, PCP tran sformed via 2,3,4,5-tetrachlorophenol (2,3,4,5-TeCP), 3,4,5-trichlorop henol (3,4,5-TCP), 3,4-dichlorophenol (3,4-DCP), 3-CP. Similarly, two different transformation pathways for HCB were observed. In the first pathway HCB transformed via pentachlorobenzene (PeCB), 1,2,3,5-tetrach lorobenzene (1,2,3,5-TeCB), 1,3,5-trichlorobenzene (1,3,5-TCB), 1,3-di chlorobenzene (1,3-DCB). In the second pathway, the transformation was , HCB, PeCB, 1,2,3,4-tetrachlorobenzene (1,2,3,4-TeCB), 1,2,4-trichlor obenzene (1,2,4-TCB), 1,4-dichlorobenzene (1,4-DCB). The results showe d that the removal of chlorine atoms from PCP and HCB were different i n sulfidogenic and methanogenic environments.