Removal of Cs+ and Sr2+ ions from simulated radioactive waste solutions using Zeolite-A synthesized from kaolin and their structural stability at high pressures

沸石 结晶度 吸附 材料科学 硅酸铝 偏高岭土 离子交换 矿物学 核化学 无机化学 化学工程 化学 离子 复合材料 粉煤灰 有机化学 催化作用 工程类
作者
M. Mahima Kumar,K. A. Irshad,Hrudananda Jena
出处
期刊:Microporous and Mesoporous Materials [Elsevier]
卷期号:312: 110773-110773 被引量:38
标识
DOI:10.1016/j.micromeso.2020.110773
摘要

Zeolite-A was synthesized from kaolin activated at 500 °C at relatively lower temperature than the studies reported in the literature.The metakaolin formed at 500 °C was used to synthesise zeolite-A by treating with 1–5 M NaOH solutions at 80–100 °C for 3–24 h under hydrothermal reaction condition. The zeolite-A was characterized by XRD, FT-IR and SEM. The percentage of crystallinity and crystallite sizes of the zeolite-A were determined from XRD analysis; the crystal system of zeolite-A was found to be cubic with space group (Fm3‾c ). The ion-exchange property of zeolite-A for Cs+ and Sr+2 was explored at ambient temperature (25 °C). The adsorption efficiency of zeolite-A is higher for Sr+2 than that of Cs+; and adsorption capacities for Cs+ and Sr2+ ions were found to be 91.51% and 99.16% respectively. Strontium substituted zeolite has higher crystallinity and lattice strain than that of caesium substituted zeolite-A. Structural stability investigations were carried out on pristine zeolite-A and its Cs+ and Sr2+ substituted analogues by using high-pressure (0.1 MPa-11.4 GPa) X-ray diffractometry technique for the first time. The pristine zeolite-A shows comparatively lower bulk modulus than that of caesium and strontium loaded zeolite. It is also seen that the compressibility is least for the strontium loaded zeolite-A (SrZtA) followed by caesium loaded zeolite-A (CsZtA) and pristine zeolite-A (ZtA) (i.e compressibility of SrZtA < compressibility of CsZtA < compressibility of ZtA).

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