Highly efficient adsorption of uranyl ions using hydroxamic acid-functionalized graphene oxide

被引:19
|
作者
Gado, Mohamed A. [1 ]
Atia, Bahig M. [1 ]
Cheira, Mohamed F. [1 ]
Elawady, Mohamed E. [1 ]
Demerdash, Mohamed [1 ]
机构
[1] Nucl Mat Author, Cairo, Egypt
关键词
adsorption; aspartic acid; graphene oxide; hydroxamic acid; uranium; URANIUM; REMOVAL; COMPOSITE; ADSORBENT; GRAPHITE; KINETICS; SORPTION; THORIUM; FILMS; PH;
D O I
10.1515/ract-2021-1063
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A chelating matrix prepared by immobilizing N-hydroxyl amine onto graphene oxide functionalized with aspartic acid (GO-HDX) was applied to recover UO22+ from their SO42- leach liquor. SEM-EDAX, FT-IR, TGA, and XRD instruments, in addition, Raman spectroscopy (IR-Raman), were used to analyze the synthesized GO-HDX. The static extraction technique optimized various physicochemical parameters that impacted the UO22+ extraction. The optimal pH, time of contact, initial concentration, GO-HDX dose, temp., foreign ions, and eluting agents were gained. The experimental equilibrium documents were assessed using Langmuir and Freundlich equations. The Langmuir equation model quite fits the investigational adsorption data with a maximum uptake of 277.78 mg/g, and it implied the attending of monolayer coverage of adsorbed molecules. Pseudo-first- and pseudo-second-order analyses were done to inspect the kinetic results. The data indicated that pseudo-second-order kinetics fit all concentrations. The intended thermodynamic factors were Delta G degrees negative values and Delta H degrees positive value. The data signified that the UO22+ extraction onto GO-HDX was spontaneous adsorption and endothermic at higher temperatures. The regeneration efficiency of GO-HDX was 98% using 1 M HCl.
引用
收藏
页码:743 / 757
页数:15
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