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dc.contributor.authorZhang, Tao
dc.contributor.authorChen, Yin
dc.contributor.authorWang, Yuru
dc.contributor.authorLe Roux, Julien
dc.contributor.authorYang, Yang
dc.contributor.authorCroue, Jean-Philippe
dc.date.accessioned2015-08-03T11:54:21Z
dc.date.available2015-08-03T11:54:21Z
dc.date.issued2014-05-06
dc.identifier.issn0013936X
dc.identifier.pmid24779765
dc.identifier.doi10.1021/es501218f
dc.identifier.urihttp://hdl.handle.net/10754/563554
dc.description.abstractPeroxydisulfate (PDS) is an appealing oxidant for contaminated groundwater and toxic industrial wastewaters. Activation of PDS is necessary for application because of its low reactivity. Present activation processes always generate sulfate radicals as actual oxidants which unselectively oxidize organics and halide anions reducing oxidation capacity of PDS and producing toxic halogenated products. Here we report that copper oxide (CuO) can efficiently activate PDS under mild conditions without producing sulfate radicals. The PDS/CuO coupled process is most efficient at neutral pH for decomposing a model compound, 2,4-dichlorophenol (2,4-DCP). In a continuous-flow reaction with an empty-bed contact time of 0.55 min, over 90% of 2,4-DCP (initially 20 μM) and 90% of adsorbable organic chlorine (AOCl) can be removed at the PDS/2,4-DCP molar ratio of 1 and 4, respectively. Based on kinetic study and surface characterization, PDS is proposed to be first activated by CuO through outer-sphere interaction, the rate-limiting step, followed by a rapid reaction with 2,4-DCP present in the solution. In the presence of ubiquitous chloride ions in groundwater/industrial wastewater, the PDS/CuO oxidation shows significant advantages over sulfate radical oxidation by achieving much higher 2,4-DCP degradation capacity and avoiding the formation of highly chlorinated degradation products. This work provides a new way of PDS activation for contaminant removal. © 2014 American Chemical Society.
dc.publisherAmerican Chemical Society (ACS)
dc.titleEfficient peroxydisulfate activation process not relying on sulfate radical generation for water pollutant degradation
dc.typeArticle
dc.contributor.departmentAdvanced Nanofabrication, Imaging and Characterization Core Lab
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentCore Labs
dc.contributor.departmentEnvironmental Science and Engineering Program
dc.contributor.departmentImaging and Characterization Core Lab
dc.contributor.departmentKAUST Solar Center (KSC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.contributor.departmentWater Desalination and Reuse Research Center (WDRC)
dc.identifier.journalEnvironmental Science & Technology
kaust.personZhang, Tao
kaust.personChen, Yin
kaust.personWang, Yuru
kaust.personLe Roux, Julien
kaust.personYang, Yang
kaust.personCroue, Jean-Philippe
dc.date.published-online2014-05-06
dc.date.published-print2014-05-20


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