Neutron flux variability at the TRIGA MARK II reactor,Ljubljana, as a parameter with applying the ko-method of NAA

Neutron-flux behaviour during irradiation should be known when applying the k_o-method of neutron activation analysis /NAA/. During two 100-hour operating periods of the TRIGA MARK II reactor, Ljubljana, the flux was measured by means of a¹⁹⁷Au/n,/¹⁹⁸Au monitor /E=411.8 keV/. Cadmium-covered irradiations were also performed to obtain the epithermal flux and thermal-to-epithermal flux ratio variations. Consistency was found between these results and the reactor operators' logbook record.     

Radon concentration in dwellings in Aomori Prefecture, Japan

To obtain an average dose from ²²²Rn to the people in Aomori Prefecture where the first Japan"s nuclear fuel cycling facilities are now under construction, we surveyed ²²²Rn concentrations in 109 dwellings in the Prefecture from 1992 to 1996. The outdoor ²²²Rn concentrations were also measured in gardens of 15 dwellings. The ²²²Rn concentrations were measured with passive ²²²Rn detectors which used a polycarbonate film for counting a-ray and could separate concentrations of ²²²Rn from ²²⁰Rn. Counting efficiencies of the detectors were calibrated with a standard ²²²Rn chamber in the Environmental Measurement Laboratory in USA and in the National Radiological Protection Board in UK. Geometric means of ²²²Rn concentration were 13 and 4.4 Bq^.m^-3 in the dwellings and outdoor, respectively. These values were consistent to nationwide survey results in Japan. The ²²²Rn concentrations in the dwellings depended on their age. The concentrations were higher in recent dwellings than in older ones. The radiation dose from ²²²Rn was estimated, taking into account the occupancy factor for inside and outside of dwellings. The annual dose was 0.32 mSv^.y^-1, and 99% of the dose came from the exposure to ²²²Rn inside the dwelling.     

Radon surveys with charcoal and liquid scintillation counting

A detection system for indoor radon using vials with activated charcoal adsorbant and liquid scintillation spectrometry for measurement has been tested thoroughly for months during different seasons. Deviation in the results of two days of exposure from the mean value were at most about ±30%. This system was chosen for a pilot project for large area surveillance in Mühlviertel, a granitic area in the federal state of upper Austria. The distribution system of the detectors is described. The measurement of more than 1200 vials within about two weeks was possible by using ultra low-level liquid scintillation counters (Quantulus). The highest value observed so far was 3150 Bq/m³. Comparing the ratios of the results from the three different measurement systems (charcoal, track etch, electret) significant but acceptable differences were found not only between track etch (3 months exposure) and activated charcoal (3 days exposure), but also between track etch and electret, which both had been exposed for three months. The data are discussed regarding the dose to the population.Note: This paper reflects the personal opinions of the authors.     

Radon Mapping of Soils in St. Elizabeth, Jamaica

Soil gas measurements of radon were made in St. Elizabeth, Jamaica using nuclear track etch detectors. The results were compared to gamma-ray spectroscopy measurements made in the laboratory on soil samples collected at the radon measurement sites. An assessment of the degree of disequilibrium of uranium and thorium was also made by comparison with neutron activation analysis, delayed neutron counting and equivalent uranium and thorium measurements. The results to date for equivalent uranium and radon show a strong correlation and indicate the possibility of soil radon mapping in Jamaica using gamma-ray spectroscopy. Three anomalous sites have been identified.     

Radon mapping in groundwater and indoor environs of Budgam,Jammu and Kashmir

Journal of Radioanalytical and Nuclear Chemistry - Radiation exposure, an inescapable share of our everyday life, primarily arises from terrestrial or cosmic sources. A small fragment of the total...     

Radon in schools and dwellings of Osijek

Indoor radon concentrations were measured in 10 821 pupils primary schools of Osijek by means of the Radhome silicon detector. The values ranged from 15 to 300 Bq/m³ with the arithmetic and geometric means of 93.4 and 70.6 Bq/m³, respectively. Ten years continuous radon measurements performed with the LR-115 nuclear track detector in three houses of different construction and town area gave means of 27, 96 and 23 Bq/m³; the indoor Rn concentration for a heating period was a factor of 1.5 higher than for the warm season. The average effective dose equivalent for the primary school pupils was 2.8 mSv/y (with occupancy factors of 0.6, 0.2 and 0.2 for home, school and outdoors, respectively). For citizens of Osijek it was 1.7 mSv/y.     

Radon concentration in groundwater of Varahi and Markandeya river basins, Karnataka State, India

The present study presents an overview of the distribution of radon (²²²Rn) activity concentration in the groundwater samples and their annual effective dose exposure in the Varahi and Markandeya command areas. Radon measurement was made using Durridge RAD-7 radon-in-air monitor, using RAD H₂O technique with closed loop aeration concept. The measured ²²²Rn activities in 16 groundwater samples of Varahi command area ranged between 0.2 ± 0.4 and 10.1 ± 1.7 Bq L⁻¹ with an average value of 2.07 ± 0.84 Bq L⁻¹, well within the EPA’s maximum contaminant level (MCL) of 11.1 Bq L⁻¹. In contrast, the recorded ²²²Rn activities in 14 groundwater samples of Markandeya command area found to vary from 2.21 ± 1.66 to 27.3 ± 0.787 Bq L⁻¹ with an average value of 9.30 ± 1.45 Bq L⁻¹. 21.4% of the samples (sample no. RMR5, RMR11 and RMR12) in the Markandeya command area exceeded the EPA’s MCL of 11.1 Bq L⁻¹ and it was found that some samples in both the command areas were found to have radon values close to MCL value. The spatial variation in the radon concentration in the Varahi and Markandeya command area were delineated by constructing the contour map. The total annual effective dose resulting from radon in groundwater of both Varahi and Markandeya command areas were significantly lower than the UNSCEAR and WHO recommended limit for members of the public of 1 mSv year⁻¹.     

Study of Radon Exhalation Rates and its correlation with Meteorological Parameters at Dumpsites in Lagos Metropolis,Nigeria

Journal of Radioanalytical and Nuclear Chemistry - Dumpsites in Lagos raise the contamination of the environment. This study aimed to determine radon exhalation rates and their changes with...     

Radon and thoron concentrations in offices and dwellings of the Gunma prefecture, Japan

Summary Aone year survey of indoor radon and thoron concentrations was carried out in offices and dwellings of the Gunma prefecture, Japan. A passive integrating radon and thoron discriminative monitor was used in the survey. The annual mean radon concentration was 22±14 Bq ^. m^-3, and ranged from 12 to 93 Bq ^. m^-3 among the 56 surveyed rooms. Radon concentration in offices was generally higher than that in the dwellings, with the arithmetic averages of 29 and 17 Bq ^. m^-3, respectively. Radon concentrations were generally lower in the traditional Japanese wooden houses than those houses built with other building materials. Seasonal variation of indoor radon was also observed in this survey. Compared to summer and autumn, radon concentrations were generally higher in spring and winter. The mean value of thoron to radon ratio was estimated to be 1.3, higher values were observed in the dwellings than in the offices. The annual effective dose from the exposure to indoor radon was estimated to be 0.47 mSv after taking the occupancy factors of offices and dwellings into account.     

Radon measurement in carbonated water with the Lucas cell and charcoal adsorption methods

There have been developed several different methods for measuring radon concentration in water which are now widely used, such as: liquid scintillation counting, Lucas cell counting, gamma and alpha spectroscopy. However, as far as the radon measurements in carbonated water are concerned, there are some issues caused by the gas excess. The aim of our work was to develop a simple method for measuring radon concentration in carbonated water that can be used for in situ measurements. Nevertheless, we propose not one, but two methods for measuring radon concentration in carbonated water. Thus, the first one is based on Lucas scintillation cells, and can be used for on-site measurements, while the second one utilizes activated charcoal adsorption, and needs a setup laboratory for gamma spectrometry measurements. For the evaluation of the methods, we compared the results of the Lucas cell-Luk3C method and of the activated charcoal method, both for non-carbonated and carbonated water. The simplest method for radon concentration determination—Lucas cell method—was successfully applied to fourteen natural carbonated water samples from Borsec to Bilbor area. The radon concentrations obtained ranged from 5.6 ± 0.5 to 39.6 ± 4.0 Bq/L, with a mean of 15.9 ± 2.6 Bq/L, these values are lower than 100 Bq/L, the maximum value recommended by the World Health Organization.     

Radon concentrations in kindergartens of Osijek and Ljubljana

Indoor radon concentrations in the kidergartens of Osijek, Croatia, have been measured with -scintillation cells, LR-115 nuclear track detectors, as well as a Radhome semiconductor detector. Average values of 50.2, 43.7 and 47 Bq m^–3 were obtained, respectively. Under the worst conditions, the annual radon effective dose equivalent was 10 mSv y^–1. Using bare and filtered LR-115 detectors, the average equilibrium factor was assessed as 0.36 indoors. Measurements of the -dose rate in the kindergartens did not show any significant correlation with the radon concentration. Indoor radon concentrations in the kindergartens of Ljubljana, Slovenia, measured by scintillation cells had an arithmetic mean and standard deviation of 228 and 143 Bq m^–3, respectively.     

Sampling, sample preparation, and analytical variability associated with testing wheat for deoxynivalenol

The variability associated with testing wheat for deoxynivalenol (DON) was measured using a 0.454 kg sample, Romer mill, 25 g comminuted subsample, and the Romer Fluoroquant analytical method. The total variability was partitioned into sampling, sample preparation, and analytical variability components. Each variance component was a function of the DON concentration and equations were developed to predict each variance component using regression techniques. The effect of sample size, subsample size, and number of aliquots on reducing the variability of the DON test procedure was also determined. For the test procedure, the coefficient of variation (CV) associated with testing wheat at 5 ppm was 13.4%. The CVs associated with sampling, sample preparation, and analysis were 6.3, 10.0, and 6.3%, respectively. For the sample variation, a 0.454 kg sample was used; for the sample preparation variation, a Romer mill and a 25 g subsample were used; for the analytical variation, the Romer Fluoroquant method was used. The CVs associated with testing wheat are relatively small compared to the CV associated with testing other commodities for other mycotoxins, such as aflatoxin in peanuts. Even when the small sample size of 0.454 kg was used, the sampling variation was not the largest source of error as found in other mycotoxin test procedures.     

Distribution of deoxynivalenol in wheat,wheat flour,bran, and gluten,and variability associated with the test procedure

Analytical data obtained on deoxynivalenol (DON) concentration in naturally contaminated wheat during processing in an industrial mill were statistically analyzed, and the distribution functions of DON concentration in lots of wheat, bran, wheat flour, and gluten were estimated. The analytical method had acceptable precision (HORRAT 0.25-0.32) for each test sample. The total variance combined sampling, sample preparation, and analytical variances were 0.188, 0.033, 0.42, and 0.0014 ppm2 for wheat, 1.93; flour, 0.99; bran, 4.68; and gluten, 0.29, respectively. The distribution function of DON contamination presented an asymmetric tail for high values of concentration in wheat grains and wheat flour; in bran it seemed to be bimodal with 2 separated peaks of different concentrations; in gluten the normal distribution function gave a reasonably good fit to empirical data. The function eta(c) = -In(-Inp), where p (c) is the cumulative distribution function was linear with c in the so-called extreme-value type I distribution and could be fitted by a cubic polynomial in c in the distributions determined for all the products. This variability and distributional information contributes to the design of better sampling plans in order to reduce the total variability and to estimate errors in the evaluation of DON concentration in lots of wheat and wheat products.     

Solubilization and location of phenethylalcohol, benzaldehyde, and limonene in lamellar liquid crystal formed with block copolymer and water

Three fragrances, phenethylalcohol, benzaldehyde, and limonene (that differ in their polarity), were solubilized in lamellar liquid crystal using the polyethylene oxide-polypropylene oxide-polyethylene oxide, (EO27PO61EO27), P104 triblock copolymer, and water. The interlayer spacing of the lamellar liquid crystal were established using small angle X-ray scattering (SAXS). The SAXS data are used to calculate the interfacial area per polyethylene oxide (PEO) block and to determine the location of each fragrance in the association structure. The results show the presence of phenethylalcohol at the interface while part of benzaldehyde contributing to the interface and the other part being located inside the polar/apolar domains. The third fragrance, limonene, did not participate in the formation of the interface and is located inside the apolar domain.     

复合熔剂熔融-ICP-AES法测定萤石中钾钠硅铁磷

采用四硼酸锂偏硼酸锂复合熔剂高频熔融炉熔融硝酸浸取方式溶解萤石,用已知含量萤石标准物质制作标准工作曲线,应用ICP-AES法联合测定萤石中硅、磷、钾、钠、铁组分含量。选择两条谱线进行分析,方法检出限在0.025～8.7mg/g之间,样品检测5次的相对标准偏差小于17.98％,测定值与证书值相吻合。     

Radon concentration in air, hot spring water, and bottled mineral water in one hot spring area in Thailand

Hot springs are famous as spa resorts throughout the world. However, these areas usually have high natural radioactivity from radon gas. In this study radon concentrations in air, hot spring water, and bottled mineral water produced in a spa area of Suan Phueng district, Ratchaburi province, Thailand were measured. Radon concentrations in air were in the range of 10–17 and 11–147 Bq/m³ for outdoor and indoor, respectively. Committed effective dose from inhale of radon were assessed and found to be in the range of 0.004–0.025, 0.25–0.6, and 1.134 mSv/y for visitor, local people and resort workers, respectively. These doses were in the range of 1.2 mSv/y regulated by UNSCEAR for the general public. Radon in hot spring water ranged from 2–154 Bq/L. Radon in bottled mineral water produced from the hot spring water were in the range of 17–22 and 0.2–0.3 Bq/L for those that stored for 7 and 90 days, respectively, after production. Radon concentration levels were in the range of the US Environmental Protection Agency reference level for radon in air which is 148 Bq/m³ and alternative maximum concentration limit (AMCL) for raw water which is 150 Bq/L. However, when considering the USEPA (Maximum concentration limit), 11 Bq/L, for radon in drinking water, the mineral water should be stored for at least 8–9 days after bottling before selling to the market.     

Outdoor 222Radon concentrations monitoring in relation with particulate matter levels and possible health effects

Air quality monitoring could potentially improve exposure estimates for use in epidemiological studies. We investigated air quality by monitoring concentrations of ²²²Rn near the ground and particulate matter (PM) with an aerodynamic diameter less than or equal to 10 μm (PM10) and 2.5 μm (PM2.5) for Bucharest-Magurele periurban area. Atmospheric radon concentrations have been continuously monitored near the ground at 1 m height as well as at 10 m height. This paper presents time-series of radon concentrations monitoring in air near the ground measured during 1 January 2011–1 January 2012 by use of solid state nuclear track detectors SSNTD CR-39, exposed for 10 days periods. The daily average atmospheric radon concentration near the ground registered at 1 m height was found to be in range of 40.25 ± 7.53 Bq/m³, which was comparable with the daily average radon concentration of 44.92 ± 9.94 Bq/m³ recorded for period 1 August 2011–20 December 2011 at 10 m height by AlphaGUARD Radon monitor. Also, was done a comparative analysis of spatio-temporal variations in time series of outdoor radon concentration and PM in two size fractions (PM10 and PM2.5) in Bucharest Magurele area for 2011 year. The predominant recorded component in PM10 was PM2.5. Observational results show that recorded yearly average PM2.5 and PM10 concentrations were 35.96 μg/m³ and 40.91 μg/m³, respectively. The average ratio of PM2.5/PM10 was 87.9 % at this sampling site. However, in densely populated Bucharest urban and suburban areas the mean daily EC limit values for PM10, PM2.5 and attached ²²²Rn are frequently exceeded leading to serious public concern during the last years. The ambient air pollution measurements like as PM10 and PM2.5 levels are used as a proxy for personal exposure levels. Have been investigated also meteorological effects on the temporal patterns of atmospheric radon and particle matter.