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    Enhanced Degradation of Nitrosamines from Water Using Zero-Valent Iron-Assisted Biological Activated Carbon

    Source: Journal of Environmental Engineering:;2021:;Volume ( 147 ):;issue: 010::page 04021038-1
    Author:
    Yanling Guo
    ,
    Yanan Cheng
    ,
    Bingli Wang
    ,
    Xueke Li
    ,
    Wanfeng Wang
    DOI: 10.1061/(ASCE)EE.1943-7870.0001892
    Publisher: ASCE
    Abstract: Nitrosamines 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.
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      Enhanced Degradation of Nitrosamines from Water Using Zero-Valent Iron-Assisted Biological Activated Carbon

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4272059
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    contributor authorYanling Guo
    contributor authorYanan Cheng
    contributor authorBingli Wang
    contributor authorXueke Li
    contributor authorWanfeng Wang
    date accessioned2022-02-01T21:48:13Z
    date available2022-02-01T21:48:13Z
    date issued10/1/2021
    identifier other%28ASCE%29EE.1943-7870.0001892.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4272059
    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.
    publisherASCE
    titleEnhanced Degradation of Nitrosamines from Water Using Zero-Valent Iron-Assisted Biological Activated Carbon
    typeJournal Paper
    journal volume147
    journal issue10
    journal titleJournal of Environmental Engineering
    identifier doi10.1061/(ASCE)EE.1943-7870.0001892
    journal fristpage04021038-1
    journal lastpage04021038-11
    page11
    treeJournal of Environmental Engineering:;2021:;Volume ( 147 ):;issue: 010
    contenttypeFulltext
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