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dc.contributor.authorFernandez-Rojo, L
dc.contributor.authorHéry, M
dc.contributor.authorLe Pape, P
dc.contributor.authorBraungardt, Charlotte
dc.contributor.authorDesoeuvre, A
dc.contributor.authorTorres, E
dc.contributor.authorTardy, V
dc.contributor.authorResongles, E
dc.contributor.authorLaroche, E
dc.contributor.authorDelpoux, S
dc.contributor.authorJoulian, C
dc.contributor.authorBattaglia-Brunet, F
dc.contributor.authorBoisson, J
dc.contributor.authorGrapin, G
dc.contributor.authorMorin, G
dc.contributor.authorCasiot, C
dc.date.accessioned2017-07-04T08:28:11Z
dc.date.available2017-07-04T08:28:11Z
dc.date.issued2017-06-22
dc.identifier.issn0043-1354
dc.identifier.issn1879-2448
dc.identifier.urihttp://hdl.handle.net/10026.1/9589
dc.description.abstract

Passive water treatments based on biological attenuation can be effective for arsenic-rich acid mine drainage (AMD). However, the key factors driving the biological processes involved in this attenuation are not well-known. Here, the efficiency of arsenic (As) removal was investigated in a bench-scale continuous flow channel bioreactor treating As-rich AMD (∼30-40 mg L-1). In this bioreactor, As removal proceeds via the formation of biogenic precipitates consisting of iron- and arsenic-rich mineral phases encrusting a microbial biofilm. Ferrous iron (Fe(II)) oxidation and iron (Fe) and arsenic removal rates were monitored at two different water heights (4 and 25 mm) and with/without forced aeration. A maximum of 80% As removal was achieved within 500 min at the lowest water height. This operating condition promoted intense Fe(II) microbial oxidation and subsequent precipitation of As-bearing schwertmannite and amorphous ferric arsenate. Higher water height slowed down Fe(II) oxidation, Fe precipitation and As removal, in relation with limited oxygen transfer through the water column. The lower oxygen transfer at higher water height could be partly counteracted by aeration. The presence of an iridescent floating film that developed at the water surface was found to limit oxygen transfer to the water column and delayed Fe(II) oxidation, but did not affect As removal. The bacterial community structure in the biogenic precipitates in the bottom of the bioreactor differed from that of the inlet water and was influenced to some extent by water height and aeration. Although potential for microbial mediated As oxidation was revealed by the detection of aioA genes, removal of Fe and As was mainly attributable to microbial Fe oxidation activity. Increasing the proportion of dissolved As(V) in the inlet water improved As removal and favoured the formation of amorphous ferric arsenate over As-sorbed schwertmannite. This study proved the ability of this bioreactor-system to treat extreme As concentrations and may serve in the design of future in-situ bioremediation system able to treat As-rich AMD.

dc.format.extent594-606
dc.format.mediumPrint-Electronic
dc.languageen
dc.language.isoen
dc.publisherElsevier BV
dc.subjectArsenic precipitation
dc.subjectBioremediation
dc.subjectIron oxidation
dc.subjectWater treatment
dc.subjectaioA genes
dc.subjectSchwertmannite
dc.titleBiological attenuation of arsenic and iron in a continuous flow bioreactor treating acid mine drainage (AMD)
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000410010500058&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.volume123
plymouth.publication-statusPublished
plymouth.journalWater Research
dc.identifier.doi10.1016/j.watres.2017.06.059
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Science and Engineering
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA06 Agriculture, Veterinary and Food Science
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/BEACh
plymouth.organisational-group/Plymouth/Research Groups/Marine Institute
dc.publisher.placeEngland
dcterms.dateAccepted2017-06-21
dc.rights.embargodate2018-6-22
dc.identifier.eissn1879-2448
dc.rights.embargoperiod6 months
rioxxterms.versionofrecord10.1016/j.watres.2017.06.059
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/under-embargo-all-rights-reserved
rioxxterms.licenseref.startdate2017-06-22
rioxxterms.typeJournal Article/Review


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