Engineered in situ biogeochemical transformation as a secondary treatment following ISCO - A field test.
Chlorine
/ metabolism
Chloroflexi
/ metabolism
Czech Republic
Desulfitobacterium
/ metabolism
Environmental Restoration and Remediation
/ methods
Ethylenes
/ metabolism
Groundwater
/ analysis
Halogenation
Iron
/ metabolism
Oxidation-Reduction
Peptococcaceae
/ metabolism
Sodium Compounds
Solvents
/ metabolism
Sulfates
/ metabolism
Tetrachloroethylene
/ analysis
Trichloroethylene
/ analysis
Water Pollutants, Chemical
/ analysis
Water Purification
/ methods
Biogeochemical transformation
Chlorinated solvents
Geochemical modelling
Indigenous microorganisms
Molecular tools
Solid phase analysis
Journal
Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
received:
14
02
2019
revised:
13
06
2019
accepted:
25
07
2019
pubmed:
3
8
2019
medline:
31
12
2019
entrez:
3
8
2019
Statut:
ppublish
Résumé
ISCO using activated sodium persulphate is a widely used technology for treating chlorinated solvent source zones. In sensitive areas, however, high groundwater sulphate concentrations following treatment may be a drawback. In situ biogeochemical transformation, a technology that degrades contaminants via reduced iron minerals formed by microbial activity, offers a potential solution for such sites, the bioreduction of sulphate and production of iron sulphides that abiotically degrade chlorinated ethenes acting as a secondary technology following ISCO. This study assesses this approach in the field using hydrochemical and molecular tools, solid phase analysis and geochemical modelling. Following a neutralisation and bioaugmentation, favourable conditions for iron- and sulphate-reducers were created, resulting in a remarkable increase in their relative abundance. The abundance of dechlorinating bacteria (Dehalococcoides mccartyi, Dehalobacter sp. and Desulfitobacterium spp.) remained low throughout this process. The activity of iron- and sulphate-reducers was further stimulated through application of magnetite plus starch and microiron plus starch, resulting in an increase in ferrous iron concentration (from <LOQ to 337 mg/l), a decrease in sulphate concentration by 74-95% and production of hydrogen sulphide (from <LOQ to 25.9 mg/l). At the same time, a gradual revival of dechlorinators and an increase in ethene concentration was also observed. Tetrachloroethene and trichloroethene concentrations decreased by 98.5-99.98% and 75.4-98.5%, respectively. A decline in chlorine number indicated that biological dechlorination contributed to CVOC removal. This study brings new insights into biogeochemical processes that, when properly engineered, could provide a viable solution for secondary treatment.
Identifiants
pubmed: 31374391
pii: S0045-6535(19)31684-4
doi: 10.1016/j.chemosphere.2019.124460
pii:
doi:
Substances chimiques
Ethylenes
0
Sodium Compounds
0
Solvents
0
Sulfates
0
Water Pollutants, Chemical
0
Trichloroethylene
290YE8AR51
Chlorine
4R7X1O2820
ethylene
91GW059KN7
Iron
E1UOL152H7
sodium persulfate
J49FYF16JE
Tetrachloroethylene
TJ904HH8SN
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
124460Informations de copyright
Copyright © 2019 Elsevier Ltd. All rights reserved.