Solubilities of individual light rare earth sulfates (lanthanum to europium) in water and H2SO4 solutions (neodymium sulfate)

被引:8
作者
Moldoveanu, G. A. [1 ]
Kolliopoulos, G. [1 ,3 ]
Judge, W. D. [2 ]
Ng, K. L. [2 ]
Azimi, G. [1 ,2 ]
Papangelakis, V. G. [1 ]
机构
[1] Univ Toronto, Dept Chem Engn & Appl Chem, 200 Coll St, Toronto, ON M5S3E5, Canada
[2] Univ Toronto, Dept Mat Sci & Engn, 184 Coll St, Toronto, ON M5S3E4, Canada
[3] Laval Univ, Dept Min Met & Mat Engn, Quebec City, PQ, Canada
关键词
Rare earth element; Sulfate; Solubility; Sulfuric acid; Hydrate; SULFURIC-ACID; ACTINIDE IONS; ELEMENTS; SYSTEMS; TEMPERATURE; RECOVERY; SODIUM;
D O I
10.1016/j.hydromet.2023.106194
中图分类号
TF [冶金工业];
学科分类号
0806 ;
摘要
Rare earth elements (REE) are critical commodities with high accessibility risk due to monopolistic practices of suppliers and increased demand. The REE ores generally require aggressive conditions to dissolve the mineral matrix, and sulfuric acid attack is the most economical preferred treatment route. The main challenge to pro-cessing REE resources efficiently is the lack of reliable and recent data regarding the solubility of individual REE sulphates in water as a function of temperature. Therefore, solubilities of light REE sulfates (La-Eu) were measured for binary REE2(SO4)3-H2O systems from 25 to 95 degrees C following both heating and cooling approaches. Additionally, solubility isotherms were determined for the ternary system Nd2(SO4)3-H2SO4-H2O system at 25, 55 and 95 degrees C from 0.05 to 0.5 M H2SO4. It was found that the solubility of light rare earth sulfates decreases with increasing temperature. Within the light REE series, solubilities increase from La to a local maximum for Pr (by one order of magnitude), followed by a sharp decrease to Nd and Sm. The solubility of Nd2(SO4)3 was moderately improved by the presence of H2SO4 , as the solubility values increase by up to 30% in 0.5 M H2SO4 compared to the no acid case. This was explained by the formation of soluble sulfate complexes due to increased concentration of SO42  ions in solution. The increase in solubility resulting from sulfuric acid addition was more significant at higher temperatures, although temperature continued to have a negative overall effect. The nature of the saturating solid phases was determined by XRD analysis on samples collected before and after phase change temperature for Ce, Nd, and Pr sulfates, while only solids collected at 25 and 95 degrees C were analyzed for the compounds known to form a single type of hydrate over the entire temperature range: usually REE2(SO4)3 center dot 8H2O except for La2(SO4)3 center dot 9H2O.
引用
收藏
页数:13
相关论文
共 48 条
  • [1] Adamas Intelligence, 2020, The 2020 Super-Recovery: EVs, Battery Metals and Rare Earths
  • [2] Barabash A. I., 1972, RUSS J INORG CHEM, V17
  • [3] Barre M., 1910, C. R. Hebdomad. Sean. 'Acad. Sci., V151, P871
  • [4] BAYANOV AP, 1981, ZH NEORG KHIM+, V26, P834
  • [5] Equilibrium versus kinetic measurements of aqueous solubility, and the ability of compounds to supersaturate in solution -: A validation study
    Box, Karl J.
    Völgyi, Gergely
    Baka, Edit
    Stuart, Martin
    Takacs-Novak, Krisztina
    Comer, John E. A.
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2006, 95 (06) : 1298 - 1307
  • [6] Cotton S., 2006, LANTHANIDE ACTINIDE
  • [7] Rare earth sulfates in aqueous systems: Thermodynamic modeling of binary and multicomponent systems over wide concentration and temperature ranges
    Das, Gaurav
    Lencka, Malgorzata M.
    Eslamimanesh, Ali
    Wang, Peiming
    Anderko, Andrzej
    Riman, Richard E.
    Navrotsky, Alexandra
    [J]. JOURNAL OF CHEMICAL THERMODYNAMICS, 2019, 131 : 49 - 79
  • [8] THERMODYNAMIC PROPERTIES OF LANTHANIDE AND ACTINIDE IONS IN AQUEOUS-SOLUTION
    DAVID, F
    [J]. JOURNAL OF THE LESS-COMMON METALS, 1986, 121 : 27 - 42
  • [9] LANTHANIDE AND ACTINIDE SULFATE COMPLEXES .I. DETERMINATION OF STABILITY CONSTANTS
    DECARVAL.RG
    CHOPPIN, GR
    [J]. JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1967, 29 (03): : 725 - &
  • [10] FOUREST B, 1984, RADIOCHIM ACTA, V36, P191