2015
DOI: 10.1016/j.scitotenv.2015.04.033
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Optimizing magnetic nanoparticles for drinking water technology: The case of Cr(VI)

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Cited by 70 publications
(39 citation statements)
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“…Moreover, it was reported that electrons can transfer from the Fe 2+ (located in the core of Fe 3 O 4 MNPs) to Cr(VI). This resulting in the reduction of Cr(VI) which can precipitate as insoluble Cr(III) hydroxide on the magnetite surface [39]. Free radical electrons can be formed due to the magnetic field generated by MNPs around themselves.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, it was reported that electrons can transfer from the Fe 2+ (located in the core of Fe 3 O 4 MNPs) to Cr(VI). This resulting in the reduction of Cr(VI) which can precipitate as insoluble Cr(III) hydroxide on the magnetite surface [39]. Free radical electrons can be formed due to the magnetic field generated by MNPs around themselves.…”
Section: Discussionmentioning
confidence: 99%
“…1). 127 Results indicate that magnetite nanoparticles may combine sufficient cost, chemical stability, improved Cr(VI) reduction ability and environmental safety after use. 79 The mechanisms of adsorption under various pH conditions, the gradual modification of ZVI during the process and the possible interferences have been reported separately for As(III) and As(V).…”
Section: Removal Of Heavy Metalsmentioning
confidence: 96%
“…In addition, in order to ensure their complete separation from treated water an expensive filtration step of nanofiltration should be included. 127 For this reason, ZVI and iron oxide nanoparticles are preferred to be used individually or as substrates for other active phases. Coagulating agents can influence the stability of nanoparticles through the production of charged hydrolytic species that neutralize surface charges on nanoparticles.…”
Section: Fate Of Used Nanoparticlesmentioning
confidence: 99%
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“…The quantitative analysis of the spectrum suggests the presence of around 68 % of captured chromium to be in the form of a Cr(III) oxide such as Cr 2 O 3 with the rest remaining to be solidified directly from the Cr(VI) state. Importantly, the formation of Cr(OH) 3 or adsorbed Cr(VI) which appear as the products of Cr(VI) removal by iron oxides can be excluded [27,28]. Therefore, the mechanism of Cr(VI) uptake can be described by the initial reduction of Cr(VI) oxyanions on surface Cu atoms, the release of consumed copper to water as Cu 2+ and the sorption of formed Cr(III) species on the regenerated Cu surface sites.…”
Section: Cr(vi) Uptake Observationsmentioning
confidence: 99%