蒙脱石、高岭石、伊利石对重金属离子吸附容量的实验研究   总被引：48，自引：4，他引：48       下载免费PDF全文

何宏平郭九皋  朱建喜杨丹 《岩石矿物学杂志》2001,20(4):573-578

在pH=4,t=23℃和微量浓度条件下,不改变离子浓度,通过增加吸附液体积进而增加体系中重金属离子含量的方法进行了蒙脱石、伊利石、高岭石对Cu2+、Pb2+、Zn2+、Cd2+、Cr3+等重金属离子吸附容量的实验研究,结果表明,3种矿物吸附容量大小顺序为蒙脱石>伊利石>高岭石,与其阳离子交换容量密切相关.Cu-蒙脱石和Cr-蒙脱石的X射线衍射结果表明,Cu2+、Cr3+通过离子交换作用进入了蒙脱石的层间.同一矿物对不同重金属离子也有不同的吸附容量蒙脱石Cr3+>Cu2+>Zn2+>Cd2+>Pb2+;高岭石Cr3+>Pb2+>Zn2+>Cu2+>Cd2+;伊利石Cr3+>Zn2+>Cd2+>Cu2+>Pb2+.  相似文献   

羟基磷灰石吸附剂去除铬黄工业废水中铅离子的研究   总被引：14，自引：1，他引：14       下载免费PDF全文

罗惠华  钟康年  刘羽 《岩石矿物学杂志》2001,20(4):587-589

羟基磷灰石吸附剂对铬黄废水中Pb^2 吸附的间歇实验结果表明：当每吨废水中吸附剂用量为200～400g时，常温搅拌60min后，在弱酸性或中性废水中，铅离子质量浓度由2.74mg/L降至0.5mg/L以下，完全符合GB8978-1996工业废水排放标准1.0mg/L。  相似文献   

低聚合羟基铁离子-蒙脱石复合体吸附砷的实验研究   总被引：15，自引：2，他引：15  

姜浩  廖立兵  王素萍 《地球化学》2002,31(6):593-601

将提纯的钙蒙脱石与羟基铁离子溶液作用，制备了低聚合羟基铁－蒙脱石复合体，用化学分析，电子探针分析，粉晶X射线衍射分析，差热分析和穆斯堡尔谱分析等手段。对蒙脱石原样，低聚合羟基铁－蒙脱石复合体和相同条件下制备的铁的含水氧化物进行了表征。在实际土壤的酸度（pH=4-7)和温度（18－40℃）条件下，进行了低聚合羟基铁－蒙脱石复合体吸附有害元素砷的实验，探讨了复合体的砷吸附能力与pH值，温度，吸附时间，砷初始浓度，离子强度间的关系，并与蒙脱石和铁的含水氧化物的砷吸附行为进行了对比，研究表明，在实验条件下，低聚合羟基铁－蒙脱石复合体对砷具有明显的亲合力，低聚合羟基铁－蒙脱石复合体吸附砷的过程有可能是地表岩石和土壤中重要的地球化学过程，是影响砷地地表，特别是土壤中迁移，富集的重要因素。  相似文献   

层柱粘土材料制备与应用研究   总被引：9，自引：1，他引：9  

周春晖  葛忠华  李春生  李小年 《矿物岩石地球化学通报》2002,21(4):242-246

简述了层柱粘土矿物材料研究与应用的现状和进展。利用粘土矿物蒙脱石作母体，通过大体积的铝、锆、硅等交联剂插层可制成层柱多孔材料，在酸催化、氧化还原催化中均有十分广阔的应用前景。研究表明，改进制备工艺后可提高层柱蒙脱石的热稳定性、比表面积和催化活性；通过酸或表面活性剂等预处理，再进行粘土的支撑，可以调节和控制层柱粘土的结构与性能；采用有机改性和模板导向等技术，可获得孔径介于大微孔和中孔之间的新型层柱粘土矿物材料，并应用于大分子催化反应与吸附，为粘土矿物材料合成和应用开辟了新方向。  相似文献   

离子交换与吸附研究方法   总被引：2，自引：0，他引：2  

张绍成 《盐湖研究》1994,2(1):74-81

综合文献资料，结合本人研究实践，对离子交换与吸附研究的一些方法做专门介绍．  相似文献   

Influence of fluid chemistry on shear-wave attenuation and velocity in sedimentary rocks   总被引：2，自引：0，他引：2  

Dung Vo-Thanh 《Geophysical Journal International》1995,121(3):737-749

  相似文献   

Surface complexation at hydrous fluorapatite     

Willis Forsling  Liuming Wu 《Aquatic Sciences - Research Across Boundaries》1993,55(4):336-346

The adsorption of H⁺, OH^– and ARS (Alizarin Red S) onto hydrous fluorapatite surfaces and Ca²⁺—ARS complexation in solution were studied by means of combined potentiometric and spectrophotometric titrations, as well as zeta potential and FT-IR measurements. Corresponding equilibrium constants of surface and solution reactions are determined. The application in flotation processes is discussed.  相似文献   

由MgMn_2O_4制备新型离子筛吸附剂及其对锂的吸附性质   总被引：1，自引：0，他引：1  

张绍成  董丽春 《盐湖研究》1993,(1)

从Mg、Mn混合溶液制备了镁锰氧化物MgMn_2O_4,并由此制得新型离子筛氧化锰HMnO(Mg)。它在碱金属及碱土金属离子中对Li~+显示了很高的选择性,pH8时分配系数Kd值顺序为Li>>Ca>Mg>K>Na,可以从实际卤水中将Li~+选择性吸附,吸附容量达20.4mg/g,用稀HCI溶液易于将吸附的Lj~+洗脱并使吸附剂再生。经用卤水和HCI五次吸附——洗脱循环,Li~+吸附容量没有降低,洗脱率总是大于90％。  相似文献   

Transport in a 2-D saturated porous medium: A new method for particle tracking   总被引：2，自引：0，他引：2  

Frédérick Delay  Hélène Housset-Resche  Gilles Porel  Ghislain de Marsily 《Mathematical Geology》1996,28(1):45-71

A new method for solving the transport equation based on the management of a large numbe of particles in a discretized 2-D domain is presented. The method uses numerical variables to represent the number of particles in a given mesh and is more complex than the 1-D problem. The first part of the paper focuses on the specific management of particles in a 2-D problem. The method also would be valid for three dimensions as long as the medium can be modeled similar to a layered system. As the particles are no longer tracked individually, the algorithm is fast and does not depend on the number of particles present. The numerical tests show that the method is nearly numerical dispersion free and permits accurate calculations even for simulations of low-concentration transport. Because each mesh is considered as a closed system between two successive time steps, it is easy to add adsorption phenomenon without any problem of numerical stability. The model is tested under conditions that are extremely demanding for its operating mode and gives a good fit to analytical solutions. The conditions in which it can be used to best advantage are discussed.  相似文献   

Mechanisms of physico-chemical interaction of mercury with river sediments from a gold mining region in Brazil: Relative mobility of mercury species     

R. Melamed  R.C. Villas Bas  G.O. Gonalves  E.C. Paiva 《Journal of Geochemical Exploration》1997,58(2-3)

Mercury accumulation in the food chain, as a consequence of gold recovery in Brazil, has been an issue of concern. Reactions of Hg in the environment are quite complex, and can involve various Hg chemical species. Laboratory experiments were carried out on Hg⁰ solubility, Hg complexation and sorption on river sediments from a gold mining region in Brazil. The reactivity and the mobility of Hg species were considered. Results indicate that methyl mercury is more mobile than ionic mercury, and that the presence of humic acid enhances drastically the solubility of Hg⁰. The soluble complex formed has a relatively lower interaction at the sediment/water interface and is more prone to spread through the aquatic environment.  相似文献