Department of Environmental Science, Zhejiang University, Hangzhou 310058, China; Zhejiang Provincial Key Laboratory of Organic Pollution Process and Control, Zhejiang University, Hangzhou 310058, China.
J Environ Sci (China). 2014 Apr 1;26(4):737-48. doi: 10.1016/S1001-0742(13)60501-X.
Removal of polycyclic aromatic hydrocarbons (PAHs), e.g., naphthalene, acenaphthene, phenanthrene and pyrene, from aqueous solution by raw and modified plant residues was investigated to develop low cost biosorbents for organic pollutant abatement. Bamboo wood, pine wood, pine needles and pine bark were selected as plant residues, and acid hydrolysis was used as an easily modification method. The raw and modified biosorbents were characterized by elemental analysis, Fourier transform infrared spectroscopy and scanning electron microscopy. The sorption isotherms of PAHs to raw biosorbents were apparently linear, and were dominated by a partitioning process. In comparison, the isotherms of the hydrolyzed biosorbents displayed nonlinearity, which was controlled by partitioning and the specific interaction mechanism. The sorption kinetic curves of PAHs to the raw and modified plant residues fit well with the pseudo second-order kinetics model. The sorption rates were faster for the raw biosorbents than the corresponding hydrolyzed biosorbents, which was attributed to the latter having more condensed domains (i.e., exposed aromatic core). By the consumption of the amorphous cellulose component under acid hydrolysis, the sorption capability of the hydrolyzed biosorbents was notably enhanced, i.e., 6-18 fold for phenanthrene, 6-8 fold for naphthalene and pyrene and 5-8 fold for acenaphthene. The sorption coefficients (Kd) were negatively correlated with the polarity index [(O+N)/C], and positively correlated with the aromaticity of the biosorbents. For a given biosorbent, a positive linear correlation between logKoc and logKow for different PAHs was observed. Interestingly, the linear plots of logKoc-logKow were parallel for different biosorbents. These observations suggest that the raw and modified plant residues have great potential as biosorbents to remove PAHs from wastewater.
从水溶液中去除多环芳烃(PAHs),例如萘、苊、菲和芘,以开发用于有机污染物去除的低成本生物吸附剂,研究了未处理和改性植物残渣对多环芳烃的去除。选择竹材、松木、松针和松皮作为植物残渣,并采用酸水解作为一种易于改性的方法。通过元素分析、傅里叶变换红外光谱和扫描电子显微镜对原始和改性生物吸附剂进行了表征。PAHs 对原始生物吸附剂的吸附等温线明显呈线性,主要受分配过程控制。相比之下,水解生物吸附剂的等温线呈非线性,这是由分配和特定相互作用机制控制的。PAHs 对原始和改性植物残渣的吸附动力学曲线很好地符合准二级动力学模型。原始生物吸附剂的吸附速率比相应的水解生物吸附剂快,这归因于后者具有更多的凝聚域(即暴露的芳核)。通过酸水解消耗无定形纤维素成分,显著提高了水解生物吸附剂的吸附能力,对于菲,萘和芘提高了 6-18 倍,对于苊提高了 6-8 倍。吸附系数(Kd)与极性指数[(O+N)/C]呈负相关,与生物吸附剂的芳香度呈正相关。对于给定的生物吸附剂,不同 PAHs 的 logKoc-logKow 之间存在正线性相关性。有趣的是,不同生物吸附剂的 logKoc-logKow 线性图是平行的。这些观察结果表明,原始和改性植物残渣具有作为生物吸附剂从废水中去除 PAHs 的巨大潜力。