2007Solvent Extraction and Ion ExchangeRequires access

Solvent Extraction and Extraction Chromatographic Separation of Am3+and Eu3+from Nitrate Medium using Cyanex®301

Arunasis Bhattacharyya, Prasanta K. Mohapatra, V. Κ. Manchanda

Open publisher page 56 citations

Abstract

The separation behavior of trivalent actinides and lanthanides from aqueous nitrate medium has been investigated using purified commercial Cyanex® 301 [bis(2,4,4‐trimethylpentyl)dithiophosphinic acid] in toluene by solvent extraction as well as by extraction chromatography. The separation studies were carried out using Am3+ and Eu3+ as the representative actinide and lanthanide ion, respectively. The stoichiometry of the extracted species as determined by the slope‐analysis method was Am(A)3 and Eu(A)2(NO3), when HA (Cyanex 301) concentration was <0.3 M. At a higher extractant concentration, the stoichiometry of the extracted Eu complex was Eu(A)3. Extraction chromatographic studies were carried out in the presence of several complexing agents that tend to influence the separation factor (D Am/D Eu) values. The solvent extraction and extraction chromatographic studies have yielded separation‐factor values of 4900 and 526, respectively.

About this research paper

What this paper is about

The separation behavior of trivalent actinides and lanthanides from aqueous nitrate medium has been investigated using purified commercial Cyanex® 301 [bis(2,4,4‐trimethylpentyl)dithiophosphinic acid] in toluene by solvent extraction as well as by extraction chromatography. The separation studies were carried out using Am3+ and Eu3+ as the representative actinide and lanthanide ion, respectively. The stoichiometry of the extracted species as determined by the slope‐analysis method was Am(A)3 and Eu(A)2(NO3), when HA (Cyanex 301) concentration was <0.3 M. At a higher extractant concentration, the stoichiometry of the extracted Eu complex was Eu(A)3. Extraction chromatographic studies were carried out in the presence of several complexing agents that tend to influence the separation factor (D Am/D Eu) values. The solvent extraction and extraction chromatographic studies have yielded separation‐factor values of 4900 and 526, respectively.

Why it matters

OpenAlex reports 56 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The separation behavior of trivalent actinides and lanthanides from aqueous nitrate medium has been investigated using purified commercial Cyanex® 301 [bis(2,4,4‐trimethylpentyl)dithiophosphinic acid] in toluene by solvent extraction as well as by extraction chromatography. The separation studies were carried out using Am3+ and Eu3+ as the representative actinide and lanthanide ion, respectively. The stoichiometry of the extracted species as determined by the slope‐analysis method was Am(A)3 and Eu(A)2(NO3), when HA (Cyanex 301) concentration was <0.3 M. At a higher extractant concentration, the stoichiometry of the extracted Eu complex was Eu(A)3. Extraction chromatographic studies were carried out in the presence of several complexing agents that tend to influence the separation factor (D Am/D Eu) values. The solvent extraction and extraction chromatographic studies have yielded separation‐factor values of 4900 and 526, respectively.

Key concepts: Chemistry, Solvent extraction, Extraction (chemistry), Radiochemistry, Actinide, Isotope separation, Nitrate, Chromatography

Related papers

Back to paper searchBrowse research topicsOriginal source
Solvent Extraction and Extraction Chromatographic Separation of Am3+and Eu3+from Nitrate Medium using Cyanex®301 — Research Paper | ScholarLens