Corrections to Kusnetz method for measurements of radon progeny concentrations in air

In 1956, H.L. Kusnetz proposed a quick method for radon progeny concentration measurement in mine atmosphere using a single gross-alpha count of a membrane-filtered air. The method is still widely used today and is based on a number of impractical assumptions. An instantaneous sampling time (less than ten seconds), is one of these assumptions that ignores the build-up and decay of the progeny on the filter paper during the sampling period, which is typically in the order of a few minutes. Of special concern is the 214Bi decay during the sampling period, since 214Po's alphas are lost during the sampling time and cannot be accounted for during the counting time. In addition, the method assumes that 214Bi activity during the counting period is constant. This inaccurate assumption can result in a smaller count rate, especially when counting times are long. Hence, underestimated working levels are expected when using Kusnetz factors without correcting for the sampling and counting times. In this technical report, exact sampling and counting time corrections to the method are provided along with the updated Kusnetz factors that correspond to common equilibrium conditions to correctly estimate the Working Level in air. Additionally, time corrections to the commonly used self-absorption correction formula and the lower level of detectability (LLD) equation used for any sample measurement are given.

Analytical Method Development and Validation for Telmisartan, Chlorthalidone and Amlodipine by UV- Spectroscopic Method.

A simple, sensitive and accurate UV- spectrophotometric absorption correction method has been developed for simultaneous determination of Telmisartan, Amlodipine and Chlorthalidone in combined tablet dosage form. Analytical method development and validation plays important role in the discovery manufacture of pharmaceuticals and development. In this paper, absorption correction method is used for multi-component analysis. The wavelengths selected for the analysis were 311nm for Telmisartan, 228nm for Chlorthalidone and 253nm for Amlodipine. Beer’s law obeyed the concentration range of 2-10 µg /ml, 2-10 µg /ml and 5-25 µg/ ml for Telmisartan, Amlodipine and Chlorthalidone. Methanol is used as a solvent. The accuracy of the method was assessed by recovery studies and was found between the range of 100% to 110% for Telmisartan, 85% to 110% for Amlodipine and 85% to 105% Chlorthalidone. The % RSD value was found to be less than 2. Thus, the method was simple, precise, economic, rapid, accurate and can be successfully applied for simultaneous determination of Telmisartan, Amlodipine and Chlorthalidone in combined tablet dosage form.

DOSIMETRY MODELING AND EXPERIMENTAL VALIDATION FOR THE PETALE PROGRAM IN THE CROCUS REACTOR

The PETALE experimental program in the CROCUS reactor intends to provide integral measurements on reactivity worth and dosimetry measurement to constrain nuclear data relative to stainless steel heavy reflectors. The experimental setup consists in eight successive plates of pure iron, pure nickel, pure chromium, or nuclear-grade stainless steel set at the close periphery of the core. The plates are interleaved with up to nine dosimeters that consist of thin activation foils with different possible materials to be sensitive to different ranges of the neutron spectrum. A precise measurement with a good estimation of the uncertainties and correlations is required, especially when comparing reaction rates, e.g. transmission measurement and/or spectral indices. The present work focuses on the validation of the dosimetry technics developed in preparation of this experimental program. Different aspects are discussed: monitors, efficiency calibration, self-absorption correction, self-shielding and nuclear data uncertainties. The different sources of uncertainties for the experiment-calculation comparisons are characterized, taking into account all the correlation between the different dosimeters. These correlations are a mandatory element for the aimed Bayesian assimilation in order to avoir overfitting when considering dosimeter providing a similar information.

Self-absorption Correction Factors: Applying A Simplified Method to Analysis of Lead-210 in Different Environment Samples by Direct Counting of Low-energy Using HPGe Detector

This study aimed to determine the self-absorption correction factors of lead-210 (210Pb) in various Syrian environment samples. Seven sediments, five soils, and four plant samples were analysed by Gamma Spectroscopy using simple and direct analysis method called Cutshall. The method is based on measuring the penetration of gamma which emitted from a standard source, prepared in the laboratory by deposition of QCYB40 Standard Solution on stainless steel disk. The source was placed on top of the studied sample and the reference air sample during the measurement. The purpose was to study the self-absorption inside each sample by calculation of its self-absorption factors without knowing its chemical composition. The self-absorption correction results for the sediment samples SE3, SE6 and SE8 ranged between 36% and 45%, and 34% to 42% for the soil samples S5 and S1, respectively. Also, for the four plant samples, it recorded variance range from 4% to 18%. This is due to the difference in the density of the G4 sample, which appeared to be very low. However, the self-absorption correction factors CF were set for the different environmental samples, and the results show that the density factor of the sample is not the only influent factor in the CF values for low energies measurement, the sample chemical composition (sample matrix) is also more effective in addition to the samples’ particle sizes.

Determination of correction factor of self-absorption for lead-210 in environment samples using spike method

In environment radiation measurement, calculation the correction factors are critical, especially for low energy measurement because of self-absorption phenomena. In this work the main purpose is to determination the self-absorption correction factors of lead-210 (210Pb) energy (46.5keV) in various environment samples (7 sediments, 5 soil) using an experimental method called Spike Method. The samples were collecting from different places in Syrian. They were prepared according to the laboratory producers starting from collecting, cleaning, drying, grounding, hemogenic and calculating the appearance density. Low-energy gamma spectroscopy HPGe was used for radiation analysis which available at the laboratories of the Protection and Safety Department - Syrian Atomic Energy Commission – Syria. The spike method depends on adding a quantity of a standard solution with a known activity which contains lead isotope 210Pb and added to the studied samples. Self-absorption correction factors (CF) calculated by the ratio of the count rate or activity of spiked and unspiked samples. The CF for sediment samples were between 29% to 54% and for soil samples, the CFs were between 38% to 56% recording correction higher than sediment samples. The results showed a relatively high self-absorption and CFs values because of the chemical composition changeable between the spiked and unspiked samples. For that, it is better to adopt other methods less expensive, give results faster, higher accuracy and do not make change in the chemical composition. The results were also showed the density factor is the most influential factor in self-absorption phenomena.