Functionalization of Zr@FMA with phosphonic acid groups for efficient separation of Th(iv) from aqueous solutions

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Jing Xiao, Linshan Peng, Ailan Ouyang, Xin Mo, Yiping Yao, Chunyan Wang and Chunpei Yan
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Abstract

A phosphonate-functionalized Zr@FMA material was prepared in this work as an adsorbent for the efficient recovery and enrichment of Th(IV) from aqueous solutions. The adsorbent, prepared by functionalizing Zr@FMA with alendronate sodium (ALS), a well-known active bisphosphonate, demonstrates good water stability and a large surface area, making it suitable for the separation and enrichment of Th(IV) in aqueous solutions. A comparison of the adsorption behavior of Th(IV) on Zr@FMA-ALS with the unfunctionalized Zr@FMA reveals that the introduction of phosphonate groups significantly enhances the maximum adsorption capacity and rate of Zr@FMA-ALS. The adsorption data aligns well with the Langmuir isotherm model, suggesting a uniform distribution of Th(IV) on the adsorbent surface in a monolayer coverage. Thermodynamic analysis indicates an endothermic and spontaneous adsorption process. Zr@FMA-ALS also shows excellent selectivity for Th(IV) over other metal ions in mixed solutions. Insights into the adsorption mechanism are provided through SEM, XPS, and FT-IR analyses, indicating that ALS molecules play a crucial role in capturing Th(IV) on the surface of Zr@FMA-ALS.

Abstract Image

用膦酸基团对 Zr@FMA 进行官能化,从水溶液中高效分离 Th(iv)
本研究制备了一种膦酸盐功能化 Zr@FMA 材料,作为从水溶液中高效回收和富集 Th(IV) 的吸附剂。该吸附剂是用著名的活性双膦酸盐阿仑膦酸钠(ALS)对 Zr@FMA 进行功能化而制备的,具有良好的水稳定性和较大的比表面积,因此适用于从水溶液中分离和富集 Th(IV)。将 Th(IV) 在 Zr@FMA-ALS 与未官能化的 Zr@FMA 上的吸附行为进行比较后发现,引入膦酸基团可显著提高 Zr@FMA-ALS 的最大吸附容量和吸附速率。吸附数据与 Langmuir 等温线模型十分吻合,表明 Th(IV) 以单层覆盖的形式均匀分布在吸附剂表面。热力学分析表明这是一个内热和自发的吸附过程。在混合溶液中,Zr@FMA-ALS 对 Th(IV) 的选择性也优于其他金属离子。通过扫描电镜、XPS 和傅立叶变换红外分析对吸附机理进行了深入研究,结果表明 ALS 分子在 Zr@FMA-ALS 表面捕获 Th(IV) 的过程中发挥了关键作用。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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