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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Clay mineral weathering and contaminant dynamics in a caustic aqueous system - II. Mineral transformation and microscale partitioning
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Clay mineral weathering and contaminant dynamics in a caustic aqueous system - II. Mineral transformation and microscale partitioning

机译:苛性水系统中的粘土矿物风化和污染物动力学-II。矿物转化和微尺度分配

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Microscopic and spectroscopic studies were conducted to assess mineral transformation processes in aqueous suspensions of illite (II), vermiculite (Vm) and montmorillonite (Mt) that were subjected to weathering in a simulated high-level radioactive tank waste leachate (0.05 M Al-T 2 M Na+, 1 M NO3- pH similar to 14, Cs+ and Sr2+ present as co-contaminants). Time series (0 to 369 d) experiments were conducted at 298 K, with initial [Cs](0) and [Sr](0) concentrations from 10(-5) to 10(-) mol kg(-). Incongruent clay dissolution resulted in an accumulation of secondary aluminosilicate precipitates identified as nitrate-sodalite, nitrate-cancrinite and zeolite X, by molecular spectroscopy and electron microscopy (XRD, IR, NMR, SEM-EDS and TEM-EDS). Contaminant fate was dependent on competing uptake to parent clays and weathering products. TEM-EDS results indicated that high II affinity for Cs was due to adsorption at frayed edge sites. The II system also comprised Sr-rich aluminous precipitates after 369 d reaction time. In Mt systems, Cs and Sr were co-precipitated into increasingly recalcitrant spheroidal precipitates over the course of the experiment, whereas contaminant association with montmorillonite platelets was less, prevalent. In contrast, Cs and Sr were found in association with weathered Vm particles despite the formation of spheroidal aluminosilicate precipitates that were comparable to those formed from Mt dissolution. Copyright (c) 2005 Elsevier Ltd.
机译:进行了显微镜和光谱研究,以评估伊利石(II),ver石(Vm)和蒙脱石(Mt)的水悬浮液中的矿物转化过程,这些悬浮液在模拟的高放废液垃圾渗滤液(0.05 M Al-T 2 M Na +,1 M NO3- pH,类似于14,Cs +和Sr2 +作为共污染物存在)。在298 K下进行了时间序列(0到369 d)实验,初始[Cs](0)和[Sr](0)浓度从10(-5)到10(-)mol kg(-)。通过分子光谱法和电子显微镜(XRD,IR,NMR,SEM-EDS和TEM-EDS),粘土的不完全溶解导致次级铝硅酸盐沉淀物的积累,这些沉淀物被鉴定为硝酸盐-苏打石,硝酸盐-钙锰矿和沸石X。污染物的命运取决于对母体粘土和风化产品的竞争吸收。 TEM-EDS结果表明,对Cs的高II亲和力归因于在磨损的边缘部位的吸附。 369 d反应时间后,II系统还包含富Sr的铝质沉淀。在Mt系统中,在整个实验过程中,Cs和Sr共沉淀为越来越难分解的球状沉淀,而与蒙脱土血小板的污染物缔合却较少,普遍。相反,尽管形成的球形硅铝酸盐沉淀物与由Mt溶解形成的球状硅酸盐沉淀物相当,但发现Cs和Sr与风化的Vm颗粒有关。版权所有(c)2005 Elsevier Ltd.

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