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- Language
- English
- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
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Received October 21, 2024
Accepted December 23, 2024
Available online June 25, 2025
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This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits
unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Most Cited
Solubility of Nd(III) Trihydroxide Solid Phase at Neutral to Weakly Alkaline Conditions: A Colorimetric and Quantitative Study
https://doi.org/10.1007/s11814-024-00372-2
Abstract
The dissolution reaction of Nd(III) trihydroxide solid phase was quantitatively investigated in the pH c range of 6.8 to 8.0
at 0.1 M NaCl medium under carbonate-free condition. Prior to the solubility experiment, the solid phase characterization
was conducted on the starting material using various analytical methods such as XRD, TA-DTG, and SEM/TEM, to obtain
stoichiometric information about the synthesized Nd(III) solid phase. For the solubility experiment, the Nd(III) solid phase
was equilibrated by means of the undersaturation approach, and the concentrations of aqueous Nd(III) species were quantifi ed
using UV–Vis absorption spectroscopy coupled with the liquid waveguide capillary fl ow cell (LWCC) and ICP-MS/OES.
After fi ltering the aqueous solution through both syringe and membrane fi lters, the measured aqueous Nd(III) concentration
indicated that no or trivial contribution from the colloidal phase of Nd(III) during the solubility experiment. Based on
chemical thermodynamic calculations using experimental results and literature data, the solubility product constant of Nd(III)
trihydroxide solid phase was determined to be log * K 0
s,0 = 18.14 ± 0.53 at infi nite dilution by applying the SIT approach ( i.e. ,
I = 0). This study demonstrated that UV–Vis absorption spectroscopy coupled with LWCC can be eff ectively employed for
the quantitative analysis of aqueous lanthanide ions at low concentrations, even without the need for additional complexing
agents.

