REE behavior and sorption on weak acid resins from buffered media

被引:24
作者
Bezzina, James P. [1 ,2 ]
Ogden, Mark D. [1 ,2 ]
Moon, Ellen M. [2 ,3 ]
Soldenhoff, Karin L. [2 ]
机构
[1] Univ Sheffield, Dept Chem & Biol Engn, Separat & Nucl Chem Engn Res SNUCER, Western Bank, Sheffield S10 2TN, S Yorkshire, England
[2] ANSTO, Locked Bag 2001, Kirrawee Dc, NSW 2232, Australia
[3] Southern Cross Univ, Southern Cross GeoSci, POB 157, Lismore, NSW 2480, Australia
关键词
Rare earths; Weak acid; Ion exchange resin; Mass transfer; Extraction; RARE-EARTH-ELEMENTS; ADSORPTION BEHAVIOR; LANTHANIDE SORPTION; EXTRACTION BEHAVIOR; AQUEOUS-SOLUTION; D113-III RESIN; METAL-IONS; SEPARATION; MECHANISM; PRODUCTS;
D O I
10.1016/j.jiec.2017.11.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rare Earth Elements (REEs) are of great importance to modern day societies. Although abundant, concentration of REE minerals in ores are generally quite low, with high concentration of impurities. To counteract this, selective extraction processes must be undertaken. Selective adsorption of REE from buffered media solutions on Purolite 5910 and Amberlite IRC86 weak acid resins has been studied. Batch experiments have been carried out on solutions containing a selection of REEs, Y3+, Fe3+ and Al3+ in unbuffered media, malic acid, formic acid, acetic acid, alanine and lactic acid to determine the best extracting media. Isotherm behavior and extraction kinetics of IRC86 were determined for acetic acid media, at the most effective pH that was determined to be 4.38. The isotherms were conducted for La3+, Sm3+, Er3+ and Y3+ determining extraction maxima of 0.29, 0.34, 0.49 and 0.60 mmol L-1, respectively, with adsorption energies increasing with the same trend. Kinetic experiments determined that mid REEs were the fastest adsorption, with light REEs and heavy REEs displaying similar half-lives and Y3+ measuring the smallest half-life out of the studied ions. (C) 2017 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:440 / 455
页数:16
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