Matches in SemOpenAlex for { <https://semopenalex.org/work/W4288045179> ?p ?o ?g. }
- W4288045179 endingPage "121796" @default.
- W4288045179 startingPage "121796" @default.
- W4288045179 abstract "• β-FeOOH phase could enhance the photocatalytic performance of FeGO aggregates. • Fe-O-C bond can serve as a channel to the separation and transfer of carrier. • •OH, H 2 O 2 and photo-generated holes dominated the oxidation of As(III) in liquid and solid phase. • As(III) was oxidized into As(V) on FeGO aggregates under light irradiation. Due to the widespread applications, graphene oxide (GO) possibly interact with natural minerals to form new heteroaggregates in the environment, which will affect the environmental processes of heavy metals as an example of arsenic. In this work, photo-oxidation and sequestration behaviors of As(III) on β-FeOOH/GO (FeGO) heteroaggregates were explored via batch and spectroscopic approaches. The formation of Fe O C bonds in FeGO was proved by X-ray photoelectron spectroscopy, which could act as an efficient carrier channel to facilitate the charrier transfer. Compared with pristine GO, the generation of β-FeOOH not only change the band structures of GO, but also improved its photoelectric performance. In the case of GO, only 18% of As(III) was photo-oxidized to less toxic As(V), and both As(III) and As(V) were completely released in the aqueous phase. For FeGO, 74% of As(III) was oxidized, 4 times higher than that in GO system. Due to β-FeOOH phase, 60% of total arsenic species was fixed on FeGO solid. It thus confirmed that β-FeOOH phase could enhance the sorption of As(III) and As(V), as well as promote the photocatalytic oxidation of As(III). The model experiments suggested that the photocatalytic activities of oxygenous groups in the heteroaggregates followed the order of carboxyl ≈ methoxy > hydroxyl > aldehyde > acetyl. Both electron paramagnetic resonance (EPR) spectroscopy and quenching tests revealed the co-existing various pathways for As(III) oxidation. Interestingly, H 2 O 2 and •OH were main oxidation species in liquid phase, whilst photogenerated holes and H 2 O 2 played the important roles during the solid-phase reaction." @default.
- W4288045179 created "2022-07-27" @default.
- W4288045179 creator A5003125273 @default.
- W4288045179 creator A5009801555 @default.
- W4288045179 creator A5014222559 @default.
- W4288045179 creator A5021678497 @default.
- W4288045179 creator A5023842403 @default.
- W4288045179 creator A5032595050 @default.
- W4288045179 creator A5066691010 @default.
- W4288045179 creator A5073070877 @default.
- W4288045179 creator A5080069873 @default.
- W4288045179 creator A5089732894 @default.
- W4288045179 date "2022-10-01" @default.
- W4288045179 modified "2023-10-16" @default.
- W4288045179 title "Photocatalytic oxidation pathways of arsenite on spontaneously forming FeOOH/GO heterostructure" @default.
- W4288045179 cites W1849523665 @default.
- W4288045179 cites W1903401465 @default.
- W4288045179 cites W1967196022 @default.
- W4288045179 cites W1986239215 @default.
- W4288045179 cites W1994895169 @default.
- W4288045179 cites W2017391008 @default.
- W4288045179 cites W2017669779 @default.
- W4288045179 cites W2017701531 @default.
- W4288045179 cites W2023249057 @default.
- W4288045179 cites W2030803996 @default.
- W4288045179 cites W2031636108 @default.
- W4288045179 cites W2038976828 @default.
- W4288045179 cites W2039806594 @default.
- W4288045179 cites W2042454875 @default.
- W4288045179 cites W2043581648 @default.
- W4288045179 cites W2058122340 @default.
- W4288045179 cites W2059573096 @default.
- W4288045179 cites W2061592336 @default.
- W4288045179 cites W2067279326 @default.
- W4288045179 cites W2078792724 @default.
- W4288045179 cites W2083023874 @default.
- W4288045179 cites W2085015653 @default.
- W4288045179 cites W2087564636 @default.
- W4288045179 cites W2089107274 @default.
- W4288045179 cites W2091708292 @default.
- W4288045179 cites W2106595669 @default.
- W4288045179 cites W2108567026 @default.
- W4288045179 cites W2123769438 @default.
- W4288045179 cites W2136334331 @default.
- W4288045179 cites W2140746165 @default.
- W4288045179 cites W2147764910 @default.
- W4288045179 cites W2149602337 @default.
- W4288045179 cites W2151642452 @default.
- W4288045179 cites W2155112057 @default.
- W4288045179 cites W2192747485 @default.
- W4288045179 cites W2207387449 @default.
- W4288045179 cites W2219681716 @default.
- W4288045179 cites W2312494039 @default.
- W4288045179 cites W2316598438 @default.
- W4288045179 cites W2317747605 @default.
- W4288045179 cites W2318574428 @default.
- W4288045179 cites W2323831705 @default.
- W4288045179 cites W2330407599 @default.
- W4288045179 cites W2468206476 @default.
- W4288045179 cites W2592834510 @default.
- W4288045179 cites W2602863255 @default.
- W4288045179 cites W2611613917 @default.
- W4288045179 cites W2613471353 @default.
- W4288045179 cites W2735379011 @default.
- W4288045179 cites W2736071212 @default.
- W4288045179 cites W2744897809 @default.
- W4288045179 cites W2786337034 @default.
- W4288045179 cites W2789594360 @default.
- W4288045179 cites W2791244691 @default.
- W4288045179 cites W2792657926 @default.
- W4288045179 cites W2804370216 @default.
- W4288045179 cites W2808438797 @default.
- W4288045179 cites W2886077595 @default.
- W4288045179 cites W2895236893 @default.
- W4288045179 cites W2904050453 @default.
- W4288045179 cites W2906846235 @default.
- W4288045179 cites W2921414362 @default.
- W4288045179 cites W2944570771 @default.
- W4288045179 cites W2973339223 @default.
- W4288045179 cites W3037671779 @default.
- W4288045179 cites W3082430081 @default.
- W4288045179 cites W3087314510 @default.
- W4288045179 cites W3087840186 @default.
- W4288045179 cites W3167048007 @default.
- W4288045179 cites W3182859284 @default.
- W4288045179 cites W3197278250 @default.
- W4288045179 cites W4210656729 @default.
- W4288045179 cites W4280600445 @default.
- W4288045179 cites W829520370 @default.
- W4288045179 doi "https://doi.org/10.1016/j.seppur.2022.121796" @default.
- W4288045179 hasPublicationYear "2022" @default.
- W4288045179 type Work @default.
- W4288045179 citedByCount "2" @default.
- W4288045179 countsByYear W42880451792023 @default.
- W4288045179 crossrefType "journal-article" @default.
- W4288045179 hasAuthorship W4288045179A5003125273 @default.
- W4288045179 hasAuthorship W4288045179A5009801555 @default.
- W4288045179 hasAuthorship W4288045179A5014222559 @default.