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Photochemistry of Dissolved Black Carbon Released from Biochar: Reactive Oxygen Species Generation and Phototransformation

机译:从生物炭释放的溶解黑碳的光化学:活性氧的产生和光转化

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摘要

Dissolved black carbon (BC) released from biochar can be one of the more photoactive components in the dissolved organic matter (DOM) pool. Dissolved BC was mainly composed of aliphatics and aromatics substituted by aromatic C-O and carboxyl/ester/quinone moieties as determined by solid-state nuclear magnetic resonance. It underwent 56% loss of absorbance at 254 nm, almost complete loss of fluorescence, and 30% mineralization during a 169 h simulated sunlight exposure. Photoreactions preferentially targeted aromatic and methyl moieties, generating CH_2/CH/C and carboxyl/ester/quinone functional groups. During irradiation, dissolved BC generated reactive oxygen species (ROS) including singlet oxygen and superoxide. The apparent quantum yield of singlet oxygen was 4.07 ± 0.19%, 2-3 fold higher than many well-studied DOM. Carbonyl-containing structures other than aromatic ketones were involved in the singlet oxygen sensitization. The generation of superoxide apparently depended on electron transfer reactions mediated by silica minerals in dissolved BC, in which phenolic structures served as electron donors. Self-generated ROS played an important role in the phototransformation. Photobleaching of dissolved BC decreased its ability to further generate ROS due to lower light absorption. These findings have significant implications on the environmental fate of dissolved BC and that of priority pollutants.
机译:从生物碳中释放出的溶解黑碳(BC)可能是溶解有机物(DOM)库中更具光活性的成分之一。通过固态核磁共振测定,溶解的BC主要由被芳香族C-O和羧基/酯/醌部分取代的脂肪族和芳香族组成。在169 h的模拟阳光照射下,它在254 nm处的吸光度损失了56%,几乎完全丧失了荧光,并且矿化了30%。光反应优先靶向芳族和甲基部分,生成CH_2 / CH / C和羧基/酯/醌官能团。在辐照期间,溶解的BC会生成包括单线态氧和超氧化物在内的活性氧(ROS)。单线态氧的表观量子产率为4.07±0.19%,比许多经过充分研究的DOM高2-3倍。单线态氧敏化涉及除芳族酮以外的含羰基的结构。超氧化物的产生显然取决于溶解于BC中的二氧化硅矿物介导的电子转移反应,其中酚类结构充当电子给体。自生ROS在光转化中起重要作用。溶解的BC的光漂白由于较低的光吸收而降低了其进一步生成ROS的能力。这些发现对溶解的BC和主要污染物的环境命运具有重大影响。

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  • 来源
    《Environmental Science & Technology》 |2016年第3期|1218-1226|共9页
  • 作者单位

    State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China;

    State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China;

    Department of Chemistry and Biochemistry, Old Dominion University, Norfolk Virginia 23529, United States;

    Department of Chemistry and Biochemistry, Old Dominion University, Norfolk Virginia 23529, United States;

    Department of Civil and Environmental Engineering, Rice University, Houston Texas 77005, United States;

    Department of Civil and Environmental Engineering, Rice University, Houston Texas 77005, United States;

    State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China;

    State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 13:58:37

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