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Sorption interaction of phenanthrene with soil and sediment of different particle sizes and in various CaCl2 solutions

机译:菲与不同粒径和CaCl2溶液对土壤和沉积物的吸附相互作用

摘要

The objective of this investigation is to evaluate the influences of natural sorbent particle size and system Ca2+ concentration,on sorption of low-polarity organic chemicals. The physicochemical properties of the different particle size soil and sediment subsamples and the surface characters of the soil and sediment samples in various CaCl2 concentrations were determined. The sorption behavior of phenanthrene (PHN) on the subsamples of different particle size and to the samples in various CaCl2 solutions was examined. Batch experiments demonstrate that the sorption capacities increase with decreased particle size for both soil and sediment. It is presumably due to the higher total organic carbon (TOC) content for the finer particles. But the enhancements in sorption coefficients are not met with the equal increases in TOC contents. The effect of Ca2+ on PHN uptake is strong in short contact time but slight in long contact time. With increasing Ca2+ concentration, the sorption capacities for Beizhai soil increase first in the low Ca2+ concentration range, and then decline. Nevertheless,. the increase of Ca2+ concentration greatly reduces the uptake of phenanthrene on Guanting sediment over the overall measured range. The different physicochemical properties, such as dissolved organic carbon (DOC) content, mineral and element composition, and surface characters, between soil and sediment may result in this discrepancy. (C) 2003 Elsevier Inc. All rights reserved.
机译:这项研究的目的是评估自然吸附剂粒径和系统Ca2 +浓度对低极性有机化学物质吸附的影响。测定了不同粒径的土壤和沉积物子样品的理化性质,以及各种浓度的CaCl2下土壤和沉积物样品的表面特征。检查了菲(PHN)在不同粒径的子样品上以及在各种CaCl2溶液中对样品的吸附行为。分批实验表明,土壤和沉积物的吸附能力都随着粒径的减小而增加。据推测,这是由于较细的颗粒具有较高的总有机碳(TOC)含量。但是,TOC含量的相等增加不能满足吸附系数的提高。 Ca2 +对PHN吸收的影响在短接触时间内很强,但在长接触时间内却很弱。随着Ca2 +浓度的增加,北寨土壤的吸附能力在低Ca2 +浓度范围内首先增加,然后下降。尽管如此,在整个测量范围内,Ca2 +浓度的增加大大降低了关亭沉积物上菲的吸收。土壤和沉积物之间的不同理化特性,例如溶解有机碳(DOC)含量,矿物质和元素组成以及表面特征,可能会导致这种差异。 (C)2003 Elsevier Inc.保留所有权利。

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    Zhou YM; Liu RX; Tang HX;

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  • 年度 2004
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