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dc.contributor.authorYanling Guo
dc.contributor.authorYanan Cheng
dc.contributor.authorBingli Wang
dc.contributor.authorXueke Li
dc.contributor.authorWanfeng Wang
dc.date.accessioned2022-02-01T21:48:13Z
dc.date.available2022-02-01T21:48:13Z
dc.date.issued10/1/2021
dc.identifier.other%28ASCE%29EE.1943-7870.0001892.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4272059
dc.description.abstractNitrosamines have become a focus of considerable research because of their carcinogenicity and environmental universality. In this study, to effectively remove nitrosamines, biological activated carbon (BAC) was acclimatized by a nitrosamine-reducing bacterial strain, and zero-valent iron (Fe0)-assisted BAC was used to degrade nitrosamines from aqueous solution. The influencing factors and degradation mechanism were investigated. Compared with activated carbon (AC), the removal efficiency of more strongly polar nitrosamines by BAC and BAC_Fe0 increased prominently (21.0%–32.3%), yet there was no change between BAC and BAC_Fe0. The highest ratios of nitrosamine degradation by BAC_Fe0 were 49.8%–99.0%, and degradation reaction kinetics conformed best to a pseudo-second-order model (R2>0.9269). The rate constants kobs for six nitrosamines ranged from 3.4×103 to 6.9 × 105 (M · s)−1. Additionally, the removal ratios and k2 of the linear nitrosamines partially scaled with their molecular weight, LogKH, and LogKow (R2=0.5661−0.952). All nitrosamines were degraded within 30  min under strong acidic conditions; the removal ratios increased by 11.2%−23.1% under anaerobic conditions, but were decreased by ∼10% in the presence of humic acid. The primary degradation products were secondary amines, methylamine, formic acid, nitrate, and nitrite resulting from the reduction of Fe0 and biodegradation by the nitrosamine-reducing bacteria.
dc.publisherASCE
dc.titleEnhanced Degradation of Nitrosamines from Water Using Zero-Valent Iron-Assisted Biological Activated Carbon
dc.typeJournal Paper
dc.journal.volume147
dc.journal.issue10
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001892
dc.journal.fristpage04021038-1
dc.journal.lastpage04021038-11
dc.page11
dc.treeJournal of Environmental Engineering:;2021:;Volume ( 147 ):;issue: 010
dc.contenttypeFulltext


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