Engineered in situ biogeochemical transformation as a secondary treatment following ISCO - A field test.


Journal

Chemosphere
ISSN: 1879-1298
Titre abrégé: Chemosphere
Pays: England
ID NLM: 0320657

Informations de publication

Date de publication:
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

124460

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Jan Němeček (J)

ENACON s.r.o., Krčská 16, 140 00, Prague 4, Czech Republic; Technical University of Liberec, Studentská 2, 461 17, Liberec, Czech Republic. Electronic address: jan.nemecek1@tul.cz.

Magda Nechanická (M)

Technical University of Liberec, Studentská 2, 461 17, Liberec, Czech Republic.

Roman Špánek (R)

Technical University of Liberec, Studentská 2, 461 17, Liberec, Czech Republic.

František Eichler (F)

Technical University of Liberec, Studentská 2, 461 17, Liberec, Czech Republic.

Josef Zeman (J)

Masaryk University, Žerotínovo nám. 617/9, 601 77, Brno, Czech Republic.

Miroslav Černík (M)

Technical University of Liberec, Studentská 2, 461 17, Liberec, Czech Republic.

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Classifications MeSH