Department of Mining and Minerals Engineering, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA.
Department of Mining and Minerals Engineering, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA.
Chemosphere. 2022 Sep;303(Pt 1):134941. doi: 10.1016/j.chemosphere.2022.134941. Epub 2022 May 12.
REE recovery tests were performed on a kaolinite and the corresponding metakaolinite using pH static leaching method. Test results show that over 90% of REEs were leached from the metakaolinite sample at pH 0.00 and 25 °C, while less than 2% of the major constituents were simultaneously extracted. Therefore, selective leaching of REEs from the metakaolinite was achieved through pH static leaching. The leaching residue was then subjected to alkaline activation for zeolites synthesis. The effects of hydrothermal temperature and incubation period under various alkaline conditions on the synthesis of zeolites were systematically investigated. The phase compositions, textual properties, and morphology of the synthesized products were characterized. Pure zeolite A with 100% relative crystallinity was successfully synthesized at 80 °C for 6 h when using 3 M NaOH as the alkaline activator. While as the synthesis conditions became increasingly harsh, the metastable zeolite A gradually transformed into more stable sodalite, and three types of zeolites, including zeolite A, sodalite, and their mixtures, were obtained. After that, various types of zeolites were applied for Ce adsorption from aqueous solutions. High purity sodalite showed a higher adsorption capacity of 53 mg/g at pH 6.0 and 25 °C as a result of the superior textual properties compared with zeolite A. The adsorption data were suitably fitted by the Langmuir isotherm and pseudo-second-order models. Findings from this study suggest that the kaolinite is a potential source for REE recovery, and the leaching residue is suitable for the synthesis of zeolites, which can be used as promising adsorbents for Ce recovery.
采用 pH 值静态浸出法对高岭石及其相应的偏高岭土进行了 REE 回收测试。测试结果表明,在 pH 值为 0.00 和 25°C 的条件下,超过 90%的 REE 从偏高岭土样品中浸出,而同时提取的主要成分不到 2%。因此,通过 pH 值静态浸出实现了 REE 从偏高岭土中的选择性浸出。浸出残渣随后进行碱性活化以合成沸石。系统研究了在各种碱性条件下水热温度和孵化期对沸石合成的影响。对合成产物的相组成、织构性质和形态进行了表征。当使用 3 M NaOH 作为碱性活化剂时,在 80°C 下反应 6 小时,成功合成了 100%相对结晶度的纯沸石 A。然而,随着合成条件变得越来越苛刻,亚稳沸石 A 逐渐转化为更稳定的方沸石,并且获得了三种沸石,包括沸石 A、方沸石及其混合物。之后,各种类型的沸石被用于从水溶液中吸附 Ce。高纯度方沸石在 pH 值为 6.0 和 25°C 时表现出较高的吸附容量 53mg/g,这是由于其与沸石 A 相比具有更好的织构性质。吸附数据通过 Langmuir 等温线和准二级模型得到了很好的拟合。本研究表明,高岭石是 REE 回收的潜在来源,浸出残渣适合合成沸石,沸石可用作 Ce 回收的有前途的吸附剂。