226Ra and 222Rn concentrations of spring waters in Balaton Upland of Hungary and the assessment of resulting doses

²²²Rn and ²²⁶Ra concentration of 18 frequently visited and regularly used, consumed spring waters on the Balaton Uplands have been measured by radon emanation method and alpha-spectrometry. ²²²Rn concentration varied between 1.5-55 Bq/l while ²²⁶Ra concentration between -601 mBq/l. The expected dose, between 14.1-119 mSv/y, has been assessed from the value of concentration supposing a daily consumption of 1 liter.     

Measurement of 222Rn and 226Ra in municipal supply tap water to evaluate their radiological impacts

ABSTRACT

Radon (²²²Rn) and its parent radionuclide Radium (²²⁶Ra) are classified as carcinogen. Human exposes to radon in water via inhalation and ingestion, although ingestion is the only way for radium to enter the human body. In this research, tap water collected from Bornova distinct was studied to determine the concentration of radon (²²²Rn) and radium (²²⁶Ra) for evaluating their radiological impact. For this reason, the annual effective doses for ingestion and inhalation were estimated. The measurements were performed using a collector chamber method. The mean concentrations of ²²²Rn and ²²⁶Ra were determined as 0.85 and 0.76 Bq/L, respectively. It can be stated that the ²²²Rn and ²²⁶Ra concentrations of tap waters here are lower than the international reference levels. Obtained concentration levels were applied to estimate annual effective dose due to the inhalation and ingestion. The dose values are also found to be lower than the recommended maximum values. On the other hand, it should be considered that consumption of these waters (2 L) and average radon and radium concentrations of water are the significant factors for estimating doses.     

Natural radioactivity of geothermal water in Beijing,China

In this work, we collected 101 geothermal water samples to investigate comprehensively the radioactivity of geothermal water in Beijing. The concentrations of gross beta, ²²⁶Ra and ²²²Rn were measured and the obtained values were in the range of 0.032–7.060, 0.023–0.363 and 0.470–29.700 Bq/L, respectively. The samples with higher concentration of ²²²Rn were found to be located near large faults. The effective dose of ²²²Rn in the air for three cases were calculated to be greater than radiation dose limit of 1 mSv/a.     

222Rn and 226Ra activity concentrations in groundwaters of southern Poland: new data and selected genetic relations

Since 2008, the authors have been conducting research into ²²²Rn and ²²⁶Ra activity concentrations in shallow circulation groundwaters in southern Poland. Measurements have been performed with a liquid-scintillation method and ultra low-level liquid-scintillation spectrometers α/β Quantulus 1220. The research carried out so far has demonstrated that in the Sudetes groundwaters with high activity concentrations of ²²²Rn and ²²⁶Ra are common. In other studied areas in southern Poland no shallow circulation groundwaters with high radon or radium concentrations have been found yet. The conducted research has demonstrated that the activity concentration of ²²²Rn dissolved in shallow circulation groundwaters in the Sudetes depends chiefly on the amount of radon, which after being released as gas from reservoir rocks is dissolved in waters flowing through these rocks. At the same time, the concentration of ²²²Rn dissolved in some shallow circulation groundwaters in the Carpathians is influenced significantly by the amount of radon produced from the decay of its parent ion ²²⁶Ra²⁺ dissolved in these waters.     

Activity concentrations of 226Ra, 228Ra, 222Rn and their health impact in the groundwater of Jordan

The activity concentrations of ²²⁶Ra, ²²⁸Ra and ²²²Rn were measured in 87 groundwater samples to estimate the activity concentrations of these radionuclides and health impact due to intake of these radionuclides in groundwater of Jordan. The mean activity concentrations of ²²⁶Ra, ²²⁸Ra and ²²²Rn in groundwater were found to be 0.293?±?0.005 Bq L^?1, 0.508?±?0.009 Bq L^?1 and 58.829?±?8.824 Bq L^?1, respectively. They give a mean annual effective dose of 0.481 mSv with mean lifetime risk of 24.599?×?10^?4, exceeding the admissible limit of 10^?4. Most of the received annual effective dose (59.15% of the total) is attributed to ²²⁸Ra.

     

Calibration and optimization of alpha-beta separation procedures for determination of radium/radon in single- and two-phase liquid scintillation systems

Liquid scintillation alpha beta discrimination technique based on pulse shape analysis (PSA) was evaluated for determination of ²²⁶Ra and ²²²Rn in water samples. In view of the significance of calibration, for the reliable and precise determination of ²²⁶Ra and ²²²Rn concentrations in water samples, calibration procedures were standardized for single and two phase systems using Quantulus 1220 liquid scintillation counter. PSA optimization and efficiency calibrations were performed using ²²⁶Ra standard rather than conventionally used pure alpha and beta standards and substantiated by measuring the activity concentrations of ²²⁶Ra and ²²²Rn in the spiked water samples.     

Determination of neodymium isotopes as burnup indicator of highly irradiated (U,Pu)O2 lmfbr fuel

A new counting method was developed to determine²²⁶Ra in environmental samples by separating the equilibrated²²²Rn into a liquid scintillator. The integral counting method, which was originally developed for isolated individual radionuclides, was extended to the mixture of²²²Rn and its daughters in equilibrium. The optimum measurement conditions were established by examining the energy spectrum, counting time and quenching effect. An absolute counting was practiced by extrapolating the integral counting rate-bias voltage curve with the highest gain to zero bias. The detection limit thus obtained was 3 to 4·10⁻¹³ Ci.     

Direct determination of 226Ra in NORM/TENORM matrices by gamma-spectrometry

Summary The main shortcoming with the procedure to determine ²²⁶Ra in a gamma spectrum of an environmental sample by means of the ²¹⁴Bi and ²¹⁴Pb photopeaks is the likelihood of ²²²Rn leakage from the sample counting vial. An option to make such determination is to disregard the ²²⁶Ra gamma-contributions to the spectrum, other than 186.2 keV (3.5%), subtracting the ²³⁵U contribution to the ²²⁶Ra+²³⁵U peak at 186 keV. The use of this option to determine directly ²²⁶Ra activity concentrations in environmental samples and in NORM/TENORM matrices will be presented and discussed.     

Solvent extraction of uranium(VI) with benzyloctadecyldimethylammonium chloride (BODMAC) from highly concentrated chloride solution

The ²²²Rn emanation fraction (EF) released from the technically enhanced naturally occurring radioactive material (TE-NORM) wastes at certain sites of petroleum and gas production was determined. The samples were analyzed by γ-ray spectrometry to determine the activity concentration of the ²²⁶Ra content, of which the ²²²Rn emanation fraction was calculated. The results showed that the ²²²Rn emanation fraction differs in the oil and gas production sites and it is independent of the activity concentration of ²²⁶Ra. This revised version was published online in August 2006 with corrections to the Cover Date.     

Radiological hazard analysis of Malaysia’s ceramic materials using generic and RESRAD-BUILD computer code approach

In this study, 52 samples of ceramic materials were studied for ²²⁶Ra, ²²²Rn, ²³²Th and ⁴⁰K natural radionuclides using high-purity germanium detector and relevant radiological hazards parameters were also appraised. Furthermore, the long-term variations of the total effective dose equivalent (TEDE) and effects of wall thickness on TEDE were established and analyzed using RESRAD-BUILD computer code. The observed percentage variations of TEDE are 2% and 8% for ²²⁶Ra and ²³²Th, respectively, while no variation observed for external dose due to ⁴⁰K. The estimated indoor doses from the studied ceramic materials are all below the recommended maximum limit.

     

A simple method for the determination of natural uranium and226Ra in waters and soils

A procedure for the determination of natural uranium and²²⁶Ra in waters and soils has been carried out and applied to the analysis of samples for environmental radiological monitoring.²²⁶Ra determination consists of co-precipitation with BaSO₄,²²²Rn emanation in toluene and finally liquid scintillation counting. Natural uranium is then determined by a fluorometric technique. This paper describes the method and the conditions that were tested to optimize it. The technique was found to be suitable for the analysis of surface and ground waters, samples from rivers, streams and lakes and soil samples, because of its few steps, short processing time, high recovery percentages and suitable detection limits.     

Assessment of inhalation exposure potential of broken uranium ore piles in low-grade uranium mine

This paper presents the assessment of inhalation exposure potential of broken uranium ore piles in different stopes of Jaduguda uranium mines of India. ²²²Rn emanation coefficient of broken uranium ore was measured in laboratory by collecting air sample from airtight glass jar containing ore sample. An attempt was also made to correlate the emanation coefficient with ²²⁶Ra content of the ore. The ²²²Rn progeny doses estimated based on radon activity concentration of broken ore, occupancy period and equilibrium ratio in different stopes were well below the prescribed limit of International Commission on Radiological Protection. The maximum ²²²Rn progeny dose contribution from broken ore piles was worked out to be 0.22 mSv year^?1. This suggests that the broken ore piles are not the significant contributor of inhalation exposure under the existing ventilation condition of Jaduguda uranium mine.     

Application of the relative uranium-series disequilibrium in soil to locate and/or confirm precisely active fault traces: A new technique

Fault traces have been previously located from measurements of ²²²Rn in soils taken a constant soil-depth across the fault trace. In this paper, we have studied the uranium-series disequilibria of the ²²⁶Ra, ²²²Rn (gas) and ²¹⁴Bi radionuclides, not only for their horizontal spatial patterns across the fault trace, but also for their vertical spatial patterns near and at the fault trace itself. Radon-222 activities in the soil-gas were measured on-site with a radiation monitor and a Lucas cell. Radium-226 and ²¹⁴Bi were determined in soil samples in the laboratory by gamma-ray spectroscopy. A new technique employing the measurement of ²²²Rn versus soil-depth shows a decrease in ²²²Rn activity at the fault trace due to the much higher soil-gas permeability as a result of the fractured soil, as well as relative larger uranium-series disequilibria, in respect to an increase in ²²²Rn activity at normal sites, where the soil is not fractured. Finally, it is suggested that fault trace detection could possibly also be performed by measuring ²¹⁴Bi in surface soils (0-100 cm) along a transect.     

Two new methods of determining radon diffusion in fish otoliths

Otoliths are bony structures found in the ears of fish and used in the²¹⁰Pb/²²⁶Ra dating method for age determination. This paper checks the assumption that²²²Rn is not lost from or added to orange roughy fish otoliths by diffusion, which would invalidate the technique. The first method of monitoring diffusion relies on measuring the gamma activity of daughter radionuclides. Otoliths were exposed to an atmosphere enriched in²²²Rn for 10 days, and the supported gamma activity inside them measured allowing for various decay corrections. The calculated radon addition was (0.5±0.5)% of the activity of the²²⁶Ra present. The second method used an alpha spectrometer and attempted to detect²²²Rn directly outgased from otoliths in the detector vacuum chamber. The results were consistent within errors with those of the first method and showed no loss or gain of²²²Rn, supporting previous estimates of a long life-span for the orange roughy. In contrast it was found that approximately 10% of²²²Rn formed in orange roughy fish scales was lost to an evacuated environment, (hence perhaps to an aqueous environment) and that for this species it could be difficult to base a dating method on analysis of scales. Nevertheless a preliminary minimum age of 57 years was obtained. The methods could be used with non-biological samples to determine²²²Rn diffusion rates.     

Study of the Energy Resolution in Alpha-Particle Spectra from Electrodeposited Radium Sources

Electrodeposited ²²⁶Ra sources were prepared and measured in order to perform a detailed study of the energy resolutions attained with two recent electrodeposition procedures for preparing spectrometric radium sources. The values of the energy resolution for the high-energy emission of ²²⁶Ra and for the single-emissions of ²¹⁰Poand ²²²Rn were calculated by fitting the data with a curve formed by the convolution of two left-handed exponentials with a Gaussian function. Significant differences between the energy resolutions for the aforementioned radionuclides were observed. The ²¹⁰Po energy resolutions were, in general, somewhat better than those obtained for ²²⁶Ra. On the contrary, the energy resolutions found for ²²²Rn were notably poorer than those obtained for ²²⁶Ra and ²¹⁰Po. These discrepancies can be satisfactorily explained by taking into consideration the distribution of these nuclides in the sources and the effect of radon diffusion involved in this type of thin deposit.     

Radiological mapping in the granodiorite area of Bergama (Pergamon)-Kozak,Turkey

As higher radiation levels are associated with granodiorite area and the maps are more practical to interpret the results of radiological survey, the distributions of the specific activities of ²²⁶Ra, ²³²Th, ⁴⁰K in soil-granite samples and indoor ²²²Rn activities throughout the granodiorite area of Bergama (Pergamon) were mapped in detail. Samples from the granites and soils underlying Kozak-Bergama (Pergamon) granodiorite area were collected and analyzed by HPGe gamma spectrometry system, while indoor radon levels in 20 dwellings of rural areas at this area were measured by the alpha track etch integrated method. This paper represents the baseline maps of natural radioactivity levels (²²⁶Ra, ²³²Th, ⁴⁰K and ²²²Rn) and corresponding absorbed dose rates from outdoors terrestrial gamma radiation.     

Radon-222 and 226Ra concentrations in mineralized groundwaters of Gorzanów (Kłodzko Basin, Sudeten Mountains, SW Poland)

This work characterizes the occurrence of radionuclides ²²²Rn and ²²⁶Ra in the mineralized groundwaters of Gorzanów. The village is situated in the Sudeten Mountains, which are known in Poland for having increased concentrations of the aforesaid radionuclides in their groundwaters. However, in Gorzanów, the measured concentrations of ²²⁶Ra were low both in the reservoir rocks and mineralized waters. Consequently, the ²²²Rn concentration in the groundwaters also turned out to be low. The ²²⁶Ra content of these waters should mainly be associated with the dissolution of this nuclide, together with other main ions, at large depths, at slightly enhanced temperature. Radon-222, on the other hand, penetrates into the water during its outflow to the surface, in the zones of intensive friable deformations near fault zones. Thus, in the groundwaters of Gorzanów, the concentrations of these nuclides, subsequent in the uranium series, do not have a common genesis and they are not correlated with each other.     

Radionuclide and chemical hazards of a radium ore revigator

A study to characterize the radionuclide and chemical components in a radium-ore revigator has been completed. Measured activities of dissolved ²²²Rn, ²²⁶Ra, and U isotopes, determined in the water using radioanalytical techniques, exceeded recommended limits in drinking-water supplies. Trace-metal concentrations, determined using inductively coupled plasma mass spectrometry, increased in the water with exposure time and exceeded recommended drinking-water limits for V and As. The contribution to, and dose from, the airborne radon-gas level in a room due to radon emanation from a revigator were evaluated. The annual committed effective dose resulting from consuming the radionuclides in the revigator water were estimated to be ~100 μSv/y for combined uranium and radium.     

Natural radioactivity in Algerian bottled mineral waters

The activity concentrations of some radionuclides in Algerian bottled mineral waters were determined using CR-39 nuclear track detectors for ²²²Rn, and a high resolution gamma-ray spectrometry for ²²⁶Ra, ²³²Th and ⁴⁰K. The mean specific activities of ²²²Rn , ²²⁶Ra, ²³¹Th and ⁴⁰K in the drinking mineral waters were 7±4 Bq^.l^-1, 26±11 mBq^.l^-1, 30±13 mBq^.l^-1 and 1±0.5 Bq^.l^-1, respectively. These values are comparable with concentrations reported for other countries. The effective doses due to intake of these radionuclides as a consequence of direct consumption of drinking mineral waters have been determined. The estimated effective doses were 56.8 mSv^.y^-1 for ²²²Rn, 3.94 mSv^.y^-1 for ²²⁶Ra, 4.45 mSv^.y^-1 for ²³²Th and 3.33 mSv^.y^-1 for ⁴⁰K. Contribution of these radionuclides to the effective dose due to ingestion and inhalation of all terrestrial radionuclides is estimated to be only 0.012%.     

Analysis of isotopic radium in thorium mill effluents

A simple and rapid method has been developed for the determination of isotopic radium, based on gamma-ray spectrometry. (228)Ra and (224)Ra are assayed by measuring the intensities of the photo-peaks in the 0.94 and the 2.62 MeV regions of the gamma-spectrum. The interference in these measurements, arising from the presence of the (226)Ra(210)Pb chain in the sample, is obviated by the almost complete expulsion of (222)Rn from the system. The precision of the method is +/-2% and +/-3 % in the determination of (228)Ra and (224)Ra respectively, the absolute sensitivities being 2 and 0.5 nCi. The method has been applied to evaluate the distribution of these isotopes in the various products of the Indian Rare-Earths Factory, Alwaye.