Efficient and Selective Removal of Palladium from Simulated High-Level Liquid Waste Using a Silica-Based Adsorbent NTAamide(C8)/SiO(2)-P

利用二氧化硅基吸附剂NTAamide(C8)/SiO(2)-P高效选择性去除模拟高放射性液体废物中的钯

阅读:1

Abstract

In order to realize the effective separation of palladium from high-level liquid waste (HLLW), a ligand-supported adsorbent (NTAamide(C8)/SiO(2)-P) was prepared by the impregnation method in a vacuum. The SiO(2)-P carrier was synthesized by in situ polymerization of divinylbenzene and styrene monomers on a macroporous silica skeleton. The NTAamide(C8)/SiO(2)-P adsorbent was fabricated by impregnating an NTAamide(C8) ligand into the pore of a SiO(2)-P carrier under a vacuum condition. The adsorption performance of NTAamide(C8)/SiO(2)-P in nitric acid medium has been systematically studied. In a solution of 0.2 M HNO(3), the distribution coefficient of Pd on NTAamide(C8)/SiO(2)-P was 1848 mL/g with an adsorption percentage of 90.24%. With the concentration of nitric acid increasing, the adsorption capacity of NTAamide(C8)/SiO(2)-P decreases. Compared to the other 10 potential interfering ions in fission products, NTAamide(C8)/SiO(2)-P exhibited excellent adsorption selectivity for Pd(II). The separation factor (SF(Pd/other metals) > 77.8) is significantly higher than that of similar materials. The interference of NaNO(3) had a negligible effect on the adsorption performance of NTAamide(C8)/SiO(2)-P, which maintained above 90%. The adsorption kinetics of Pd(II) adsorption on NTAamide(C8)/SiO(2)-P fits well with the pseudo-second order model. The Sips model is more suitable than the Langmuir and Freundlich model for describing the adsorption behavior. Thermodynamic analysis showed that the adsorption of Pd(II) on NTAamide(C8)/SiO(2)-P was a spontaneous, endothermic, and rapid process. NTAamide(C8)/SiO(2)-P also demonstrated good reusability and economic feasibility.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。