从水稻秸秆中提取主要组分——木质素、纤维素、半纤维素,利用元素分析和红外光谱对其性质进行了表征,并研究了芘在秸秆及其3种组分上的吸附行为.结果表明,各组分性质差异很大,木质素具有较高的芳香性和较低的极性,而纤维素和半纤维素具有较高的极性和脂肪性.不同组分对芘的吸附等温线均符合Freundlich方程,但吸附能力因其结构的差异而不同,木质素对芘的吸附能力最强,吸附容量KF为5.04×104,比纤维素高100倍左右,而芘在半纤维素上的吸附能力略低于纤维素.低浓度(水相平衡浓度ce=0.01Sw)下,秸秆对芘的吸附主要受木质素的控制,而且分配系数Kd略低于按照木质素质量分数计算的预测值,可能是由于木质素的烷基和芳香结构被周围的极性结构所覆盖.但在高浓度(ce=0.5Sw)时,秸秆对芘的吸附高于各组分的加和,芘向秸秆其他组分的分配作用不能忽略.芘在木质素上的吸附表现为非线性(非线性指数,n=0.89),而其它3种吸附剂对芘的吸附更趋向于线性(n〉0.96).n值与芳香性呈负相关关系,而与极性呈正相关关系,表明芳香性导致的特殊作用力是造成吸附非线性的主要原因.有机碳标化分配系数Koc随吸附剂芳香性的增强而增大,但随极性的增强而减小.
Main constituents(lignin,cellulose and hemicelullose) were extracted from rice straw,and characterized by elemental analysis and Diffuse Reflectance Infrared Fourier Transform Spectroscopy(DRIFT).Sorption of pyrene on rice straw and its main constituents was studied.The results showed that there are great differences in the properties of the three constituents,with lignin of higher aromaticity and lower polarity,while cellulose and hemicellulose of greater polarity and aliphaticity.Sorption of pyrene also differed a lot due to the varied characteristics of the sorbents.All isotherms were fitted well with Freundlich equation.Lignin showed the greatest sorption capacity for pyrene,with KF being 5.04 × 104,approximately 100 times greater than that of cellulose.Sorption of pyrene on hemicellulose was even a little smaller than that on cellulose.At low solute aqueous concentration(ce = 0.01 Sw),the sorption of pyrene on rice straw was controlled by lignin,and sorption coefficient(Kd) was a little smaller than that predicted by the Kd value on lignin and its mass fraction.This suggested that some sorption sites such as alkyl and aromatic centers were covered when the lignin existed mixed in the rice straw.But at high concentration(ce = 0.5 Sw),the Kd value of pyrene on rice straw was markedly greater than the sum of those on three constituents,suggesting that partition on other constituents could not be neglected.Moreover,pyrene sorption isotherm on lignin was nonlinear(Freundlich exponent,n = 0.89),while sorption on the other three sorbents was more linear(n 0.96).A negative relationship between n and aromaticity was observed,which illustrates that specific effect related with aromaticity is the main reason for nonlinearity.Organic carbon normalized sorption coefficients(Koc) increased with increasing aromaticity and decreased with increasing polarity of the sorbents.