A Study of the Residual 39Ar Content in Argon from Underground Sources

The discovery of argon from underground sources with significantly less 39Ar than atmospheric argon was an important step in the development of direct-detection dark matter experiments using argon as the active target. We report on the design and operation of a low background detector with a single phase liquid argon target that was built to study the 39Ar content of the underground argon. Underground argon from the Kinder Morgan CO2 plant in Cortez, Colorado was determined to have less than 0.65% of the 39Ar activity in atmospheric argon.Comment: 21 pages, 10 figure

Species sensitivity of zeolite minerals for uptake of mercury solutes

The uptake of inorganic Hg2+ and organometallic CH3Hg+ from aqueous solutions by 11 different natural zeolites has been investigated using a batch distribution coefficient (Kd) method and supported by a preliminary voltammetric study. The effect of mercury concentration on theKd response is shown over an environmentally appropriate concentration range of 0.1-5 ppm inorganic and organometallic Hg using a batch factor of 100 ml g−1 and 20 h equilibration. Analcime and a Na-chabazite displayed the greatest methylmercury uptakes (Kd values at 1.5 ppm of 4023 and 3456, respectively), with mordenite as the smallest at 578. All uptake responses were greater for methylmercury than for the inorganic mercuric nitrate solutions, suggesting a distinctive sensitivity of zeolites to reaction with different types of solute species. It is likely that this sensitivity is attributable to the precise nature of the resultant Hg-zeolite bonds. Additionally, both the Si-Al ratio and the Na content of the initial natural zeolite samples are shown to influence the Kd responses, with positive correlations between Kd and Na content for all zeolites excluding mordenite

Functionalized NaA Nanozeolites Labeled with 224,225Ra for Targeted Alpha Therapy

The 223Ra, 224Ra, and 225Ra radioisotopes exhibit very attractive nuclear properties for application in radionuclide therapy. Unfortunately the lack of appropriate bifunctional ligand for radium is the reason why these radionuclides have not found application in receptor-targeted therapy. In the present work, the potential usefulness of the NaA nanozeolite as a carrier for radium radionuclides has been studied. 224Ra and 225Ra, a-particle emitting radionuclides, have been absorbed in the nanometer-sized NaA zeolite (30–70 nm) through simple ion exchange. 224,225Ra-nanozeolites exhibited very high stability in solutions containing physiological salt, EDTA, amino acids, and human serum. To make NaA nanozeolite particles dispersed in water their surface was modified with a silane coupling agent containing poly(ethylene glycol) molecules. This functionalization approach let us covalently attach a biomolecule to the NaA nanozeolite surface.JRC.E.5-Nuclear chemistr

Spatially uniform calibration of a liquid xenon detector at low energies using 83m-Kr

A difficult task with many particle detectors focusing on interactions below ~100 keV is to perform a calibration in the appropriate energy range that adequately probes all regions of the detector. Because detector response can vary greatly in various locations within the device, a spatially uniform calibration is important. We present a new method for calibration of liquid xenon (LXe) detectors, using the short-lived 83m-Kr. This source has transitions at 9.4 and 32.1 keV, and as a noble gas like Xe, it disperses uniformly in all regions of the detector. Even for low source activities, the existence of the two transitions provides a method of identifying the decays that is free of background. We find that at decreasing energies, the LXe light yield increases, while the amount of electric field quenching is diminished. Additionally, we show that if any long-lived radioactive backgrounds are introduced by this method, they will present less than 67E-6 events/kg/day in the next generation of LXe dark matter direct detection searchesComment: 9 pages, 9 figures. Accepted to Review of Scientific Instrument

Low-Background gamma counting at the Kimballton Underground Research Facility

The next generation of low-background physics experiments will require the use of materials with unprecedented radio-purity. A gamma-counting facility at the Kimballton Underground Research Facility (KURF) has been commissioned to perform initial screening of materials for radioactivity primarily from nuclides in the 238U and 232Th decay chains, 40K and cosmic-ray induced isotopes. The facility consists of two commercial low-background high purity germanium (HPGe) detectors. A continuum background reduction better than a factor of 10 was achieved by going underground. This paper describes the facility, detector systems, analysis techniques and selected assay results.Comment: 7 pages, 7 figures. Submitted to NIM

Adsorption of uranium and thorium on new adsorbent prepared from Moroccan oil shale impregnated with phosphoric acid

Attention has been focused recently on the production of new adsorbents from Moroccan oil shale of Tarfaya (layer R3) by chemical activation with phosphoric acid and its application in wastewaters treatment. The optimal conditions for the preparation were searched and the tests of adsorption of uranium and thorium ions were affected. The best product was obtained by used of the ratio of activated agent/precursor equal 3 and activation of the mixture in air at 250°C during two hours after prepocessing at 120°C in air. Under these conditions the maximal adsorption capacity of methylene blue and specific area (SBET) of the new adsorbent were 526 mg/g and 630 m2/g, respectively. A batch mode experiment was used to explore the performances of this adsorbent for the removal of the U and Th from aqueous solutions prepared from UO2(NO3)2.6H2O and Th(NO3)4.5H2O. The adsorption parameters for the two radioelements were determined by application of the Langmuir, Freundlich and Elovich models

A passive sampling method for radiocarbon analysis of atmospheric CO₂ using molecular sieve

Radiocarbon (14C) analysis of atmospheric CO2 can provide information on CO2 sources and is potentially valuable for validating inventories of fossil fuel-derived CO2 emissions to the atmosphere. We tested zeolite molecular sieve cartridges, in both field and laboratory experiments, for passively collecting atmospheric CO2. Cartridges were exposed to the free atmosphere in two configurations which controlled CO2 trapping rate, allowing collection of sufficient CO2 in between 1.5 and 10 months at current levels. 14C results for passive samples were within measurement uncertainty of samples collected using a pump-based system, showing that the method collected samples with 14C contents representative of the atmosphere. δ13C analysis confirmed that the cartridges collected representative CO2 samples, however, fractionation during passive trapping means that δ13C values need to be adjusted by an amount which we have quantified. Trapping rate was proportional to atmospheric CO2 concentration, and was not affected by exposure time unless this exceeded a threshold. Passive sampling using molecular sieve cartridges provides an easy and reliable method to collect atmospheric CO2 for 14C analysis