Membranes for the Capture and Screening of Waterborne Plutonium Based on a Novel Pu-Extractive Copolymer Additive

This contribution describes the fabrication of plutonium-adsorptive membranes by non-solvent induced phase separation. The dope solution comprised poly(vinylidene fluoride) (PVDF) and a Pu-extractive copolymer additive of PVDF-g-poly(ethylene glycol methacrylate phosphate) (EGMP) in dimethylformamide (DMF). The effects of casting conditions on membrane permeability were determined for PVDF membranes prepared with 10 wt% PVDF-g-EGMP. Direct-flow filtration and alpha spectrometry showed that membranes containing the graft copolymer could recover Pu up to 59.9 ± 3.0% from deionized water and 19.3 ± 3.5% from synthetic seawater after filtering 10 mL of 0.5 Bq/mL 238Pu. SEM-EDS analysis indicated that the graft copolymer was distributed evenly throughout the entire depth of the copolymer membranes, likely attributing to the tailing observed in the alpha spectra for 238Pu. Despite the reduction in resolution, the membranes exhibited high Pu uptake at the conditions tested, and new membrane designs that promote copolymer surface migration are expected to improve alpha spectrometry peak energy resolutions. Findings from this study also can be used to guide the development of extractive membranes for chromatographic separation of actinides from contaminated groundwater sources.

A fast strategy to sequentially separate and determine 90Sr, 210Pb and 210Po in water samples using Sr resin

This study presents a rapid and novel sequential separation strategy based on extraction chromatography for determining 90Sr, 210Pb and 210Po in drinking water samples. It involves the use of Sr resin for the separation and then liquid scintillation counting and alpha spectrometry for the determination. The experimental results obtained showed that the proper acidic solution to quantitatively retain the aforementioned radionuclides is 3 M HNO3. The optimum eluents were determined for obtaining quantitative recoveries (70–80%) of 90Sr, 210Pb and 210Po. The method was validated with intercomparison water samples and is satisfactory in terms of minimum detectable activities, which are 50% lower than that established in RD 314/2016.

Determination of 234U and 238U Activities in Soil by Liquid Scintillation and High-Resolution Alpha Spectrometry

Uranium is a radioactive element with a special presence in the rocks, waters, sediments, soils, and plants at the state of Chihuahua. The activity ratio of 238U/234U is used to explain the uranium transport by surface water and its deposition in arid environments. In this work, the activity concentration of natural U isotopes is determined by PERALS liquid scintillation and high-resolution alpha spectrometry (AS, Canberra camera 7401VR) in the Environmental Radiological Surveillance Laboratory (LVRA) at CIMAV, Chihuahua. Uranium is extracted from soils through the scintillating liquid extractor URAEX for PERALS, with chemical recovery (CR) of 80 - 85 %, and through the ion exchange resin UTEVA + electrode position by the Hallstadius method, with CR of 85 - 90 %, for AS. The procedures of 234U and 238U activity concentration (AC) determination in soils were validated by their application to the certified reference material IAEA-375. The resulting values were in the reference range of the certified or informative values. Both procedures were applied to 6 representative soil samples, with AC of the same order of magnitude or greater, and similar CR and compatible results. Both procedures are satisfactory for the purposes of LVRA research and in general.

Rapid determination of 210Pb and 210Po by sequential cloud point extraction for environmental monitoring

A new sequential cloud point extraction (CPE) procedure was developed and validated for the determination of 210Pb and 210Po by ICP-MS/MS and alpha spectrometry, respectively. Two distinct CPE systems using...