Photochemical Transformation and Catalytic Activity of Dissolved Black Nitrogen Released from Environmental Black Carbon

被引:32
作者
Lian, Fei [1 ,2 ]
Zhang, Yikang [1 ,2 ]
Gu, Shiguo [1 ,2 ]
Han, Yaru [1 ,2 ]
Cao, Xuesong [1 ,2 ]
Wang, Zhenyu [1 ,2 ]
Xing, Baoshan [3 ]
机构
[1] Jiangnan Univ, Inst Environm Proc & Pollut Control, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Environm & Civil Engn, Wuxi 214122, Jiangsu, Peoples R China
[3] Univ Massachusetts, Stockbridge Sch Agr, Amherst, MA 01003 USA
基金
中国国家自然科学基金;
关键词
REACTIVE OXYGEN; ENHANCED ADSORPTION; ORGANIC-MATTER; BIOCHAR; AGGREGATION; NANOTUBES; SORPTION; WASTE; GENERATION; REDUCTION;
D O I
10.1021/acs.est.1c00392
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Biomass combustion results in the formation and wide distribution of black carbon (BC) in soils, wherein the dissolved fractions are among the most active components. Although the presence of dissolved black nitrogen (DBN) in BC has been identified, its environmental behavior and implication are not understood. This study investigated the photochemical transformation and catalytic activity of DBN under simulated solar irradiation. DBN is more easily transformed than dissolved BC due to its photoactive heteroaromatic N structure, and the half-life of DBN produced at 500 degrees C (8.6 h) is two times shorter than that of the dissolved BC counterpart (23 h). Meanwhile, solar irradiation is favorable for the homoaggregation of DBN. During irradiation, DBN generates not only reactive oxygen species (e.g., O-1(2), O-2(-), and (OH)-O-center dot) but also reactive nitrogen species (mainly (ON)-O-center dot), which account for its higher photocatalytic degradation of bisphenol A than dissolved BC. These findings shed new light on the impact of heteroatoms on the phototransformation and activity of BC as well as cycling of N in terrestrial systems.
引用
收藏
页码:6476 / 6484
页数:9
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