Burn-up measurement on an irradiated mixed oxide (MOX) test fuel pellet was carried out through measurements on the dissolver solution by HPLC-Thermal Ionization Mass Spectrometric (TIMS) technique. The studies carrie...Burn-up measurement on an irradiated mixed oxide (MOX) test fuel pellet was carried out through measurements on the dissolver solution by HPLC-Thermal Ionization Mass Spectrometric (TIMS) technique. The studies carried out using HPLC as well as TIMS for quantification of burn-up value are described. While in one case, both the separation and determination of elements of interest (U, Pu and Nd) were carried out by HPLC;in another case, TIMS technique was used to quantify them from the HPLC separated fractions.The rapid separation procedures developed in our laboratory earlier were employed to isolate pure fractions of the desired elements. The individual lanthanide fission products (La to Eu) were separated from each other using dynamic ion-exchange chromatographic technique whereas uranium and plutonium were separated from each other using reversed phase chromatographic technique. The pure fractions of U, Pu and Nd obtained after HPLC separation procedure for “spiked” and “unspiked” dissolver solutions were used in TIMS measurements for the first time in our laboratory. In TIMS analysis, isotopic abundances of uranium, plutonium and neodymium fractions obtained from HPLC separation procedure on an “unspiked” fuel sample were measured. For the determination of U, Pu and Nd by isotopic dilution mass spectrometric technique (IDMS), known quantities of tracers enriched in 238U, 240Pu and 142Nd were added to the pre-weighed dissolver solution and subjected to HPLC separation procedures. The isotope ratios viz. 142Nd/(145Nd +146Nd), 238U/233U and 240Pu/239Pu in the pertinent “spiked” fractions were subsequently measured by TIMS. The spikes were pre-standardized in our laboratory employing reverse isotopic dilution technique against the standard solutions available in our laboratory (for 238U, 239Pu and 142Nd, standard solutions of 233U, 239Pu (of higher abundance than in the sample) and 150Nd were employed as spikes). The burn-up values from duplicate spiking experiments were computed based on the summation of 145Nd + 146Nd. The concentrations of neodymium, uranium and plutonium were also measured using HPLC with post-column derivatisation technique using aresenazo(III) as the post-column reagent. The atom % burn-up computed from HPLC and TIMS techniques were in good agreement.展开更多
Supercritical Fluid Extraction (SFE) is emerging as a powerful technique in the extraction of metal ions. In the present study, the extraction of nitrates of uranium and thorium was carried out using supercritical car...Supercritical Fluid Extraction (SFE) is emerging as a powerful technique in the extraction of metal ions. In the present study, the extraction of nitrates of uranium and thorium was carried out using supercritical carbon dioxide (Sc-CO2) modified with various organophosphorous compounds such as dialkylalkyl phosphonates, trialkyl phosphates and trialkyl phosphine oxides in the presence of co-solvents such as methanol, dichlormethane and n-hexane. The influence of ligand and co-solvent on the extraction of the metal nitrates was studied in detail. These studies have established that co-solvent plays an important role in the extraction as well as fractionation of uranium and thorium nitrates. Polar co-solvent, methanol provided faster extraction without fractionation whereas the non-polar solvent, e.g. n-hexane provided some fractionation of metal nitrates though the extraction kinetics was slower.展开更多
文摘Burn-up measurement on an irradiated mixed oxide (MOX) test fuel pellet was carried out through measurements on the dissolver solution by HPLC-Thermal Ionization Mass Spectrometric (TIMS) technique. The studies carried out using HPLC as well as TIMS for quantification of burn-up value are described. While in one case, both the separation and determination of elements of interest (U, Pu and Nd) were carried out by HPLC;in another case, TIMS technique was used to quantify them from the HPLC separated fractions.The rapid separation procedures developed in our laboratory earlier were employed to isolate pure fractions of the desired elements. The individual lanthanide fission products (La to Eu) were separated from each other using dynamic ion-exchange chromatographic technique whereas uranium and plutonium were separated from each other using reversed phase chromatographic technique. The pure fractions of U, Pu and Nd obtained after HPLC separation procedure for “spiked” and “unspiked” dissolver solutions were used in TIMS measurements for the first time in our laboratory. In TIMS analysis, isotopic abundances of uranium, plutonium and neodymium fractions obtained from HPLC separation procedure on an “unspiked” fuel sample were measured. For the determination of U, Pu and Nd by isotopic dilution mass spectrometric technique (IDMS), known quantities of tracers enriched in 238U, 240Pu and 142Nd were added to the pre-weighed dissolver solution and subjected to HPLC separation procedures. The isotope ratios viz. 142Nd/(145Nd +146Nd), 238U/233U and 240Pu/239Pu in the pertinent “spiked” fractions were subsequently measured by TIMS. The spikes were pre-standardized in our laboratory employing reverse isotopic dilution technique against the standard solutions available in our laboratory (for 238U, 239Pu and 142Nd, standard solutions of 233U, 239Pu (of higher abundance than in the sample) and 150Nd were employed as spikes). The burn-up values from duplicate spiking experiments were computed based on the summation of 145Nd + 146Nd. The concentrations of neodymium, uranium and plutonium were also measured using HPLC with post-column derivatisation technique using aresenazo(III) as the post-column reagent. The atom % burn-up computed from HPLC and TIMS techniques were in good agreement.
文摘Supercritical Fluid Extraction (SFE) is emerging as a powerful technique in the extraction of metal ions. In the present study, the extraction of nitrates of uranium and thorium was carried out using supercritical carbon dioxide (Sc-CO2) modified with various organophosphorous compounds such as dialkylalkyl phosphonates, trialkyl phosphates and trialkyl phosphine oxides in the presence of co-solvents such as methanol, dichlormethane and n-hexane. The influence of ligand and co-solvent on the extraction of the metal nitrates was studied in detail. These studies have established that co-solvent plays an important role in the extraction as well as fractionation of uranium and thorium nitrates. Polar co-solvent, methanol provided faster extraction without fractionation whereas the non-polar solvent, e.g. n-hexane provided some fractionation of metal nitrates though the extraction kinetics was slower.