College of Environmental Science and Engineering, North China Electric Power University, Beijing, 102206, China; State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, 100875, China.
State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, 100875, China.
Environ Pollut. 2018 May;236:745-753. doi: 10.1016/j.envpol.2018.02.015. Epub 2018 Feb 15.
Chemical composition and pollutant sorption of biochar-derived organic matter fractions (BDOMs) are critical for understanding the long-term environmental significance of biochar. Phenanthrene (PHE) sorption by the humic acid-like (HAL) fractions isolated from plant straw- (PLABs) and animal manure-based (ANIBs) biochars, and the residue materials (RES) after HAL extraction was investigated. The HAL fraction comprised approximately 50% of organic carbon (OC) of the original biochars. Results of XPS and C NMR demonstrated that the biochar-derived HAL fractions mainly consisted of aromatic clusters substituted by carboxylic groups. The CO cumulative surface area of BDOMs excluding PLAB-derived RES fractions was obviously lower than that of corresponding biochars. The sorption nonlinearity of PHE by the fresh biochars was significantly stronger than that of the BDOM fractions, implying that the BDOM fractions were more chemically homogeneous. The BDOMs generally exhibited comparable or higher OC-normalized distribution coefficients (K) of PHE than the original biochars. The PHE logK values of the fresh biochars correlated negatively with the micropore volumes due to steric hindrance effect. In contrast, a positive relationship between the sorption coefficients (K) of BDOMs and the micropore volumes was observed in this study, suggesting that pore filling could dominate PHE sorption by the BDOMs. The positive correlation between the PHE logK values of the HAL fractions and the aromatic C contents indicates that PHE sorption by the HAL fractions was regulated by aromatic domains. The findings of this study improve our knowledge of the evolution of biochar properties after application and its potential environmental impacts.
生物炭衍生有机质(BDOM)的化学组成和污染物吸附对于理解生物炭的长期环境意义至关重要。本研究考察了源于植物秸秆(PLABs)和动物粪便(ANIBs)生物炭的腐殖酸样(HAL)组分以及 HAL 萃取后剩余物质(RES)对菲(PHE)的吸附作用。HAL 组分约占原始生物炭有机碳(OC)的 50%。XPS 和 C NMR 的结果表明,生物炭衍生的 HAL 组分主要由取代羧酸基团的芳香簇组成。除 PLAB 衍生的 RES 组分外,BDOMs 的 CO 累积表面面积明显低于相应的生物炭。新鲜生物炭对 PHE 的吸附非线性明显强于 BDOM 组分,这表明 BDOM 组分在化学上更加均匀。BDOMs 通常表现出与原始生物炭相当或更高的 OC 归一化分配系数(K)。新鲜生物炭的 PHE logK 值与微孔体积呈负相关,这是由于空间位阻效应。相比之下,在本研究中,BDOMs 的吸附系数(K)与微孔体积之间存在正相关关系,这表明孔填充可能主导 BDOMs 对 PHE 的吸附。HAL 组分的 PHE logK 值与芳香 C 含量呈正相关,表明 HAL 组分对 PHE 的吸附受芳香结构域调控。本研究的结果提高了我们对生物炭应用后性质演变及其潜在环境影响的认识。