首页> 外文学位 >ADSORPTION OF COPPER AND CADMIUM ONTO SOILS: INFLUENCE OF ORGANIC MATTER (ISOTHERM, COMPLEXATION, TRACE METALS).
【24h】

ADSORPTION OF COPPER AND CADMIUM ONTO SOILS: INFLUENCE OF ORGANIC MATTER (ISOTHERM, COMPLEXATION, TRACE METALS).

机译:铜和镉在土壤上的吸附:有机物(等温线,络合物,微量金属)的影响。

获取原文
获取原文并翻译 | 示例

摘要

The sorption of copper and cadmium by three arid-zone soils at low solution concentrations (i.e. <10 mmol m('-3) for copper and <50 (mu)mol m('-3) for cadmium) was studied. The majority of previous studies of metal sorption by soils reported in the literature were conducted at higher resolution concentrations of metals. Garc(')ia-Miragaya observed previously that data for cadmium sorption at low solution concentrations conformed to the van Bemmelen-Freundlich equation. McLaren et al. reported earlier that data for copper sorption by soils could be fit to the Langmuir equation. Sorption isotherms in the present study were characterized by an S-curve which is defined by an initial slope that increases with metal concentration.; Preliminary kinetic studies indicated that copper sorption reactions were completed within one hour. The sigmoidal character of the isotherm was found always to be greater for copper than for cadmium and greatest for the soil highest insoluble organic carbon. The distribution function, K(,d), for cadmium was a monotonically decreasing function of the amount of metal sorbed. Values of K(,d) first increased and then decreased with increasing amounts of copper sorbed. Although increasing sorbent concentration decreased copper sorption, the shape of the isotherm remained unchanged.; A soil separate was prepared by successive extractions with a low electrolyte solution in order to remove most of the soluble organic matter. L-curve isotherms were observed for copper and cadmium sorption by the soil separate; the surface exhibited a high affinity for the metals relative to aqueous solution. The addition of a commercially prepared fulvic acid to the soil separate reproduced an S-curve for copper sorption. Likewise, addition of fulvic acid to the unamended soils increased the sigmoidal character of the copper isotherms. A kinetic study suggested that either fulvic acid was not sorbed by the soil separate within the time period of experiment (24 hours) or that it was readily desorbed by copper. Copper was readily desorbed by fulvic acid at concentrations that are found in the soil environment. It was proposed that soluble organic ligands can form nonsorbing, soluble complexes with copper and cadmium.; Cupric ion measurements indicated that the sorption isotherm for cupric ion was an L-curve isotherm regardless of the concentration of soluble organic matter. This suggested that the copper-fulvate complex was not sorbed by the soil surface. A mathematical description of the S-curve isotherm was derived from the combination of two macroscopic models involving the binding of metal by soluble organic ligands and metal sorption.
机译:研究了三种干旱区土壤在低溶液浓度下(即铜<10 mmol m('-3)和镉<50μmolm('-3)的吸附对铜和镉的影响)。文献中报道的大多数以前的土壤吸附金属的研究都是在较高分辨率的金属上进行的。 Garc(')ia-Miragaya先前观察到,低溶液浓度下的镉吸附数据符合van Bemmelen-Freundlich方程。迈凯轮等。早些时候报道说,土壤吸附铜的数据可能符合Langmuir方程。在本研究中,吸附等温线的特征是S曲线,该曲线的初始斜率随金属浓度的增加而增加。初步的动力学研究表明,铜吸附反应在一小时内完成。发现铜的等温线的S形特征总是比镉的大,对于土壤中最高的不溶性有机碳最大。镉的分布函数K(,d)是金属吸附量的单调递减函数。 K(,d)的值首先随着吸附的铜量的增加而增加,然后减小。尽管增加吸附剂浓度会降低铜的吸附量,但等温线的形状保持不变。通过用低电解质溶液连续萃取来制备土壤分离物,以除去大部分可溶有机物。分开土壤观察到L曲线等温线对铜和镉的吸附;相对于水溶液,表面对金属表现出高亲和力。向分离的土壤中添加商业制备的黄腐酸可产生用于铜吸附的S曲线。同样,向未改良的土壤中添加黄腐酸会增加铜等温线的S形特征。动力学研究表明,富里酸在实验时间内(24小时)没有被单独的土壤吸收,或者很容易被铜吸收。富勒酸容易以土壤环境中发现的浓度解吸铜。有人提出,可溶性有机配体可以与铜和镉形成不吸附的可溶性络合物。铜离子的测量表明,不管可溶性有机物的浓度如何,铜离子的吸附等温线都是L曲线等温线。这表明富铜的铜络合物没有被土壤表面吸收。 S曲线等温线的数学描述来自两个宏观模型的组合,其中涉及可溶性有机配体与金属的结合以及金属的吸附作用。

著录项

  • 作者

    LECLAIRE, JOSEPH PAUL.;

  • 作者单位

    University of California, Riverside.;

  • 授予单位 University of California, Riverside.;
  • 学科 Geochemistry.
  • 学位 Ph.D.
  • 年度 1985
  • 页码 267 p.
  • 总页数 267
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 地质学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号