Groenewold G S, Ingram J C, McLing T, Gianotto A K, Avci R
Idaho National Engineering and Environmental Laboratory, Idaho Falls, Idaho 83415-2208.
Anal Chem. 1998 Feb 1;70(3):534-9. doi: 10.1021/ac9705172.
Soil particles exposed to CsI solutions were analyzed by imaging time-of-flight secondary ion mass spectrometry and also by scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS). The results showed that Cs(+) could be detected and imaged on the surface of the soil particles readily at concentrations down to 160 ppm, which corresponds to 0.04 monolayer. Imaging revealed that most of the soil surface consisted of aluminosilicate material. However, some of the surface was more quartzic in composition, primarily SiO(2) with little Al. It was observed that adsorbed Cs(+) was associated with the presence of Al on the surface of the soil particles. In contrast, in high SiO(2) areas of the soil particle where little Al was observed, little adsorbed Cs(+) was observed on the surface of the soil particle. Using EDS, Cs(+) was observed only in the most concentrated Cs(+)-soil system, and Cs(+) was clearly correlated with the presence of Al and I. These results are interpreted in terms of multiple layers of CsI forming over areas of the soil surface that contain substantial Al. These observations are consistent with the hypothesis that the insertion of Al into the SiO(2) lattice results in the formation of anionic sites, which are then capable of binding cations.
通过飞行时间二次离子质谱成像以及扫描电子显微镜/能量色散X射线光谱法(SEM/EDS)对暴露于碘化铯(CsI)溶液中的土壤颗粒进行了分析。结果表明,在低至160 ppm的浓度下(相当于0.04个单分子层),能够轻易在土壤颗粒表面检测到并成像Cs(+)。成像显示,大部分土壤表面由铝硅酸盐物质组成。然而,部分表面的成分更富含石英,主要是SiO₂且几乎不含铝。据观察,吸附的Cs(+)与土壤颗粒表面铝的存在有关。相反,在土壤颗粒中几乎观察不到铝的高SiO₂区域,在土壤颗粒表面几乎观察不到吸附的Cs(+)。使用EDS,仅在Cs(+)浓度最高的Cs(+) - 土壤体系中观察到Cs(+),并且Cs(+)与铝和碘的存在明显相关。这些结果可解释为在土壤表面含有大量铝的区域形成了多层CsI。这些观察结果与以下假设一致:铝插入SiO₂晶格会导致形成阴离子位点,然后这些位点能够结合阳离子。