Deng Yawen, Yan Caixia, Nie Minghua, Ding Mingjun
School of Geography and Environment, Key Laboratory of Poyang Lake Wetland and Watershed Research, Ministry of Education, Jiangxi Normal University, 99 Ziyang Road, Nanchang, 330022, China.
Environ Sci Pollut Res Int. 2021 Feb 24. doi: 10.1007/s11356-021-12723-1.
Dissolved organic matter (DOM) released from soil (SDOM) and biochar (BDOM) plays an important role in the fate of pollutants for the application of biochar in soil remediation. However, little attention has been paid to the impact of DOM on the adsorption of soil and/or biochar-bisphenol A (BPA) system. Hence, batch sorption experiments combined with quenching titration experiments were processed to reveal these behaviors and complexation mechanisms based on red soil and corn straw biochar. Moreover, multiple spectral technologies and methods were also introduced including ultraviolet-visible, three-dimensional excitation-emission matrix, synchronous fluorescence spectrum, two-dimensional correlation spectroscopy (2D-COS), and parallel factor analysis. Isothermal adsorption results showed that the non-linearity and the adsorption capacity both increased after the addition of biochar, indicating that biochar could improve the surface adsorption capacity of the sorption system. Besides, the sorption capacity of BPA decreased for soil while increased for biochar after removal of the water-extractable DOM. 2D-COS analysis showed that the protein-like components preferentially occurred for both SDOM and BDOM under BPA surrounding. In addition, C2 (humic-like), C4 (tyrosine-like), and C5 (tryptophan-like) in the two DOMs were all involved in the quenching reaction with BPA, with C4 and C5 having higher quenching degree than C2, suggesting that protein-like substances had stronger affinity quenching effect with BPA. This study highlighted the significance of fluorescence property for DOM, which can extend the knowledge of the fate of pollutants in the application of biochar.
土壤释放的溶解有机物(SDOM)和生物炭释放的溶解有机物(BDOM)在生物炭用于土壤修复时对污染物的归宿起着重要作用。然而,DOM对土壤和/或生物炭-双酚A(BPA)体系吸附的影响却很少受到关注。因此,进行了批量吸附实验和猝灭滴定实验,以揭示基于红壤和玉米秸秆生物炭的这些行为和络合机制。此外,还引入了多种光谱技术和方法,包括紫外可见光谱、三维激发-发射矩阵光谱、同步荧光光谱、二维相关光谱(2D-COS)和平行因子分析。等温吸附结果表明,添加生物炭后,吸附的非线性和吸附容量均增加,表明生物炭可提高吸附体系的表面吸附能力。此外,去除水可提取DOM后,土壤对BPA的吸附容量降低,而生物炭对BPA的吸附容量增加。2D-COS分析表明,在BPA存在的情况下,SDOM和BDOM中均优先出现类蛋白成分。此外,两种DOM中的C2(类腐殖质)、C4(类酪氨酸)和C5(类色氨酸)均参与了与BPA的猝灭反应,C4和C5的猝灭程度高于C2,表明类蛋白物质与BPA具有更强的亲和猝灭作用。本研究突出了DOM荧光特性的重要性,可拓展生物炭应用中污染物归宿的相关知识。