Analysis of 226Ra, 232Th and 40K in soil samples for the assessment of the average effective dose

The activity concentrations of the natural radionuclides namely ²³⁸Ra, ²³²Th and ⁴⁰K are measured for soil samples collected from different locations of Faridkot and Mansa districts of Punjab. HPGe detector, based on high-resolution gamma spectrometry system is used for the measurement of activity concentration. The range of activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in the soil from the studied areas varies from 21.42 Bq kg⁻¹ to 40.23 Bq kg⁻¹, 61.01 Bq kg⁻¹ to 142.34 Bq kg⁻¹ and 227.11 Bq kg⁻¹ to 357.13 Bq kg⁻¹ with overall mean values of 27.17 Bq kg⁻¹, 95.22 Bq kg⁻¹ and 312.76 Bq kg⁻¹, respectively. Radium equivalent activities are calculated for the analyzed samples to assess the radiation hazards arising due to the use of these soil samples in the construction of dwellings. The absorbed dose rate calculated from activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K ranges between 9.87 and 18.55, 38.01 and 88.68 and 9.40 and 14.79 nGy h⁻¹, respectively. The total absorbed dose in the study area ranges from 61.10 nGy h⁻¹ to 112.86 nGy h⁻¹ with an average value of 84.80 nGy h⁻¹. The calculated values of external hazard index (H _ex) for the soil samples of the study area range from 0.36 to 0.68. Since these values are lower than unity, according to the Radiation Protection 112 (European Commission, 1999) report, soil from these regions is safe and can be used as construction material without posing any significant radiological threat to population. The corresponding average annual effective dose for indoor and outdoor measured in the study area are 0.42 mSv and 0.10 mSv respectively.      

Radon exhalation rate in Chhatrapur beach sand samples of high background radiation area and estimation of its radiological implications

Chhatrapur beach placer deposit, situated in a part of the eastern coast of Orissa, is a newly discovered high natural background radiation area (HBRA) in India. The sand samples containing heavy minerals, were collected from Chhatrapur region by the grab sampling method at an interval of ∼1 Km. Radon exhalation rates were measured by “Sealed Can Technique” using LR-115 type type II in the sand samples containing heavy minerals collected from the beach. Radon activity is found to vary from 1177.1 to 4551.4 Bq m-3 whereas the radon exhalation rate varies from 423.2 to 1636.3 mBq m⁻²h⁻¹ with an average value of 763.9 mBq m⁻²h⁻¹. Effective dose equivalent in sand samples estimated from exhalation rate varies from 49.9 to 193.0 μSv y⁻¹ with an average value of 90.1 μSv y⁻¹. From the activity concentration of ²³⁸U, ²³²Th and ⁴⁰K computed radium equivalent is found to vary from 864.0 to 11471.5 Bq kg⁻¹ with an average value of 3729.0 Bq kg⁻¹. External hazard index, H_ex range from 2.3 to 31.0 with a mean value of 10.1, which is quite high. This value supports the conclusion based on high mean absorbed gamma dose rate in air due to the naturally occurring radionuclides as 1627.5 nGy h⁻¹. A positive correlation has been found between U concentration and radon exhalation rate in the sand samples. The use of sand as construction material may pose a radiation risk to ambient environment.      

Natural radioactivity and radiation hazards assessment of soil samples from the area of Tuzla and Lukavac,Bosnia and Herzegovina

The results of activity concentration measurements of natural occurring radioactive nuclides ²³⁸U, ²³⁵U, ²³²Th, ²²⁶Ra, and ⁴⁰K in surface soil samples collected in the area of cities Tuzla and Lukavac, northeast region of Bosnia and Herzegovina were presented. Soil sampling was conducted at the localities that are situated in the vicinity of industrial zones of these cities. The measured activity was in the range from (8?±?4) to (95?±?28) Bq kg^–1 for ²³⁸U, from (0.41?±?0.06) to (4.6?±?0.7) Bq kg^–1 for ²³⁵U, from (7?±?1) to (66?±?7) Bq kg^–1 for ²³²Th, from (6?±?1) to (55?±?6) Bq kg^–1 for ²²⁶Ra, and from (83?±?12) to (546?±?55) Bq kg^–1 for ⁴⁰K. In order to evaluate the radiological hazard of the natural radioactivity for people living near industrial zones, the absorbed dose rate, the annual effective dose and the radium equivalent activity have been calculated and compared with the internationally approved values.     

Interpolated mapping and investigation of environmental radioactivity levels in soils and mushrooms in the Middle Black Sea Region of Turkey

The activity concentration of natural (²³⁸U, ²³²Th, and ⁴⁰K) and artificial (¹³⁷Cs) radionuclides was determined in 50 samples (obtained from the same station) from various species of mushrooms and soil collected from the Middle Black Sea Region (Turkey). The activities of ²³⁸U, ²³²Th, ⁴⁰K, and ¹³⁷Cs were found as 84 ± 16, 45 ± 14, 570 ± 28, and 64 ± 6?Bq?kg^–1 (dry weight), respectively, in the mushroom samples and as 51?±?6, 41?±?6, 201?±?11, and 44?±?4?Bq?kg^–1, respectively, in the soil samples for the entire area of study. The results of all radionuclide activity measurements, except those of ²³⁸U and ²³²Th in the mushroom samples, are consistent with previous studies. In the soil samples, the mean values of ²³⁸U and ²³²Th are above the world mean, and the activity mean of ⁴⁰K is below the world mean. Finally, the activity estimation was made with both the soil and mushroom samples for unmeasured points within the study area by using the ordinary kriging method. Radiological distribution maps were generated.     

Uranium, radium and radon exhalation studies in some soil samples using plastic track detectors

Radium concentration and radon exhalation rate have been measured in soil samples collected from some areas belonging to upper Siwaliks of Kala Amb, Nahan and Morni Hills of Haryana and Himachal Pradesh states, India using LR-115 type II plastic track detectors. Uranium concentration has also been determined in these soil samples using fission track registration technique. Radium concentration has been found to vary from 5.30 to 31.71 Bq.kg⁻¹, whereas uranium concentration varies from 33.21 to 76.26 Bq.kg⁻¹. The radon exhalation rate in these samples varies from 216.87 to 1298.00 mBq.m⁻²hr⁻¹ (6.15 to 36.80 mBq.kg⁻¹.hr⁻¹). Most of the samples have uranium concentration above the worldwide average concentration of 35 Bq.kg⁻¹. A good correlation (R ² = 0.76) has been observed between uranium concentration and radon exhalation rate in soil. The values of uranium, radium and radon exhalation rate in soil are compared with that from the adjoining areas of Punjab.     

Thoron (220Rn) in the indoor environment and work places

Ever since studies on uranium miners established the presence of a positive risk coefficient for the occurrence of lung cancer in miners exposed to elevated levels of ²²²Rn and its progeny, there was a great upsurge of interest in the measurement of ²²²Rn in the environment. Subsequently, considerable data is being generated on the levels of ²²²Rn in the environment across the worlds and is being periodically reported by UNSCEAR reports. In contrast to this, data pertaining to ²²⁰Rn in indoors and workplace environment is scaree due to the genral perception that its levels are negligible due to its shorter half life, and subsequently its contribution to the total inhalation dose is ignored, in the presence of other significant sources of natural radiation. This may not be true. Globally many locations have higher levels of natural background radiation due to elevated levels of primordial radio nuclides in the soil and their decay products like radon (²²²Rn), and thoron (²²⁰Rn) in the environment. Of late, technologically enhanced naturally occurring radioactive material has also contributed to the burden of background radiation. It is estimated that inhalation of ²²²Rn, ²²⁰Rn and their short lived progenies contribute more than 54% of the total natural background radiation dose received by the general population. ²²⁰Rn problem exists in industries which use thorium nitrate. Including India, lamps using thoriated gas mantles are still being used for indoor and outdoor lighting and by hawkers in rural as well as urban areas. Considering the fact that large amount of thorium nitrate is being handled by these industries, contribution to the inhalation dose of workers from ²²⁰Rn gas emanated and build up of the progeny in ambient air may also be quite significant. In this paper current status of ²²⁰Rn levels in the indoor environment and workplaces as well as in other industries where large amount of ²³²Th is being handled is being summarized. Methods of measurement and reported levels are also summarized.     

Statistical relationship between activity concentrations of radionuclides 226Ra, 232Th, 40K,and 137Cs and geological formations in surface soil of Jordan

An extensive study was conducted to determine the activity concentrations of natural and artificial radionuclides ²²⁶Ra, ²³²Th, ⁴⁰K, and ¹³⁷Cs in soil samples of each governate of Jordan. A total of 370 samples have been measured using a high-purity germanium detector. The activity concentration for ²²⁶Ra, ²³²Th, ⁴⁰K, and ¹³⁷Cs has mean values of 42?±?3, 23?±?3, 309?±?21, and 3.7?±?0.9 Bq kg^–1, respectively. The highest mean activity concentration for ²²⁶Ra was found to be 138?±?4 Bq kg^–1 in the Alkarak governate. In the Ajloun and Jarash governates, the highest mean activity concentration was 35?±?3 Bq kg^–1 for ²³²Th, and 14.2?±?1.9 Bq kg^–1 for ¹³⁷Cs, respectively. Geological influence on the activity concentrations was investigated using the one-way analysis of variance (ANOVA) and independent samples. The ANOVA results indicate that there are strong significant differences between the activity concentrations of ²³²Th, ⁴⁰K, and ¹³⁷Cs based on geological formations the radionuclides occur. The main contribution to gamma dose rate was due to ²²⁶Ra activity concentration. Radium equivalent and external hazard index are associated with a mean value of 98 Bq kg^–1, and 0.266, respectively.     

Short-lived isomers in 211Rn and 210Rn

The following mean lives of excited states in ²¹¹Rn and ²¹⁰Rn have been measured: ²¹¹Rn: 8169 + Δ' keV, (τ = 3.3(3) ns), 7400 + Δ' keV (2,1(5) ns), 6101 + Δ' (41(2) ns), 5247 + Δ keV (5(2) ns), 3244 + Δ keV (3.9(8) ns), 2651 + Δ keV (9.6(4) ns); ²¹⁰Rn: 8555 + Δ keV (2.6(3) ns), 4994 + Δ keV (19(1) ns), 1665 keV (15.0(15) ns). Some theoretical implications of these measurements for the structure of ²¹¹Rn and ²¹⁰Rn are discussed.     

The determination of concentrations of radioisotopes in some granite samples in Turkey and their radiation hazards

The primordial radionuclides activity concentrations (²²⁶Ra, ⁴⁰K and ²³²Th) are measured in some granite samples in this study. The collected granite materials are analyzed with NaI(Tl) gamma-ray spectrometry. The specific activity of ²²⁶Ra, ²³²Th and ⁴⁰K values are in range 2.60?±?0.10 to 178.9?±?0.6?Bq?kg^?1, 1.46?±?0.10 to 162.50?±?0.75?Bq?kg^?1 and 19.8?±?0.3 to 579.7?±?2.8?Bq?kg^?1 respectively. The radium’s equivalent activity, annual effective dose, absorbed dose rate, hazard index, radioactivity level index, activity utilization’s index and exposure rate are calculated for determination of radiological risk. The concentration of ²²⁶Ra (in the 71.4% of samples), ²³²Th (in the 71.4% of samples) and ⁴⁰K (in the 14.3% of samples) in the granite samples are higher than average radioactivity concentrations of this radio-isotopes defined by ICRP (35.0, 30.0 and 400.0?Bq?kg^?1, respectively).     

Fast determination of uranium and radium in waters of variable composition

The effects of uranium and its progeny radium are known to be harmful and their measurements in drinking water are necessary for careful monitoring. Fast and accurate methods for determination of uranium and radium in water samples with various salinity and activities concentrations have been developed. High Resolution Inductively Coupled Plasma Mass Spectrometry is used for direct measurement of uranium. Calibration is performed with ²³⁸U standards and ²⁰⁹Bi is used as internal standard to correct the matrix effects and plasma instability. The radium is determined by photon electron rejected alpha liquid spectrometry after a chemical separation procedure that includes co-precipitation of radium with barium sulphate, transformation of the sulphate to carbonate and extraction of radium in the scintillation cocktail. The minimal detectable activities of 3.5×10⁻⁸ Bq kg⁻¹ for uranium and 2.3×10⁻⁴ Bq kg⁻¹ for radium are obtained.     

Natural radioactivity measurements in Pahang State,Malaysia

This study was aimed at providing the baseline data of terrestrial gamma dose rates and natural radioactivity to assess the corresponding health risk in the ambient environment of the Pahang State. Terrestrial gamma radiation (TGR) from 640 locations was measured with the mean value found to be 176?±?5 nGy h^?1. Ninety-eight soil samples were analysed using a high-purity germanium detector (HPGe), and the mean concentrations of the radionuclides ²²⁶Ra, ²³²Th and ⁴⁰K are 110?±?3, 151?±?5 and 542?±?51 Bq kg^?1, respectively.²²⁶Ra and ²³²Th concentrations were found to be three times the world average, while that of ⁴⁰K is quite higher than the world average value. The acid-intrusive geological formation has the highest mean concentrations for ²²⁶Ra (215?±?6 Bq kg^?1), ²³²Th (384?±?12 Bq kg^?1) and ⁴⁰K (1564?±?153 Bq kg^?1). The radium equivalent activities (Req) and the external hazard index (Hex) for the various soil types were also calculated. Some of the soil types were found to have values exceeding the internationally recommended levels of 370 Bq kg^?1 and the unity value, respectively.     

Radioactivity concentrations in topsoil samples from the Thrace region of Turkey and assessment of radiological hazard

The activity concentrations of gamma emitting radionuclides were measured in surface soil samples from the Thrace region. ²³²Th, ²³⁸U, ²²⁶Ra, ⁴⁰K and ¹³⁷Cs activities and physico-chemical parameters of the soil samples were determined in samples collected from 73 sampling stations. Radionuclide concentrations measured were compared with those found in the samples from other locations of Turkey and from different countries. The average activity concentrations of ²³²Th, ²³⁸U, ²²⁶Ra, ⁴⁰K and ¹³⁷Cs were found to be 24.71 ± 8.79, 22.30 ± 7.93, 32.09±12.44, 509.00±160.05, 32.74±29.24 Bq kg^?1, respectively. The mean value of the annual effective dose equivalent from the outdoor terrestrial gamma radiation was calculated as 57.2 μ Sv.     

Variation of radon concentrations in soil and groundwater and its correlation with radon exhalation rate from soil in Budhakedar, Garhwal Himalaya

Radon was measured in soil-gas and groundwater in the Budhakedar area of Tehri Garhwal, India in summer and winter to obtain the seasonal variation and its correlation with radon exhalation rate. The environmental surface gamma dose rate was also measured in the same area. The radon exhalation rate in the soil sample collected from different geological unit of Budhakedar area was measured using plastic track detector (LR-115 type II) technique. The variation in the radon concentration in soil-gas was found to vary from 1098 to 31,776 Bq.m⁻³ with an average of 7456 Bq.m⁻³ in summer season and 3501 to 42883 Bq.m⁻³ with an average of 17148 Bq.m⁻³ in winter season. In groundwater, it was found to vary from 8 to 3047 Bq.l⁻¹ with an average value 510 Bq.l⁻¹ in summer and 26 to 2311 Bq.l⁻¹ with an average value 433 Bq.L⁻¹ in winter. Surface gamma dose rate in the study area varied from 32.4 to 83.6 μR.h⁻¹ with an overall mean of 58.7 μ-R.h⁻¹ in summer and 34.6 to 79.3 μR.h⁻¹ with an average value 58.2 μR.h⁻¹ in winter. Radon exhalation rate from collected soil samples was found to vary from 0.1 × 10⁻⁵ to 5.7 × 10⁻⁵ Bq.kg⁻¹.h⁻¹ with an average of 1.5 × 10⁻⁵ Bq.kg⁻¹.h⁻¹ in summer season and 1.7 × 10⁻⁵ to 9.6 × 10⁻⁵ Bq.kg⁻¹.h⁻¹ with an average of 5.5 × 10⁻⁵ Bq.kg⁻¹.h⁻¹. A weak negative correlation was observed between radon exhalation rate from soil and radon concentration in the soil. Radon exhalation rate from the soil was also not found to be correlated with the gamma dose rate, while it shows a positive correlation with radon concentration in water in summer season. Inter-correlations among various parameters are discussed in detail.      

Natural radioactivity levels and associated health hazards from the terrestrial ecosystem in Rosetta branch of the River Nile,Egypt

Twenty soil and 25 sediment samples were collected from the banks and bottom of the River Nile in the surroundings of biggest cities located close to it. Natural radioactivity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K have been evaluated for all samples by means of γ spectrometric analysis. The radioactivity levels of soil and sediment samples fall within the internationally recommended values. Nevertheless, high natural background radiation zones are detected in the Kafr El-Zayat region due to the presence of a fertilizer factory, and in the Rosetta region due to the presence of black sand deposits. The absorbed dose rate, the γ index and excess life time cancer risk are calculated. High values for some of the radiation health parameters are detected in the Kafr El-Zayat and Rosetta regions representing a serious problem to public health because the soil and sediment are used as constructing material for buildings. Furthermore, the isotope analysis of uranium for representative collected sediment samples via α spectrometry showed average specific activities of 18.7?±?3.6, 0.087?±?0.0038 and 18.6?±?3.8 Bq kg^–1 for ²³⁴U, ²³⁵U and ²³⁸U, respectively. In general, these values confirm the balance in the isotopic abundance of U isotopes.     

Radioactivity in waters of Mt. Etna (Italy)

Radioactivity in underground waters from Mt. Etna was investigated on the basis of 13 samples. The samples were collected from springs, wells and galleries around the volcano. Water from nine out of thirteen intakes is used for consumption. Activity concentration of uranium isotopes ^234,238U, radium isotopes ^226,228Ra and radon ²²²Rn were determined with the use different nuclear spectrometry techniques. The measurements of radium and radon activity concentration were performed with the use of a liquid scintillation counter. The determination of uranium isotopes was carried out with the use of alpha spectrometry. All samples show uranium concentration above Minimum Detectable Activity (MDA), with the highest total uranium (²³⁴U + ²³⁸U) activity concentration equal to 130 mBq/l. For radium isotopes, all samples except one showed the activity concentration below MDA. Radon activity concentration was within the range from 1 to 13 Bq/l, hence these waters can be classified as low-radon waters.     

Radioactivity of sand,groundwater and wild plants in northeast Sinai,Egypt

The radioactivity levels are poorly studied in non-coastal arid regions. For this reason, 38 locations covering an area of about 350 km² in northeast Sinai, Egypt, were investigated by γ-ray spectroscopy. Moderately significant correlations among ²³⁸U, ²³⁴Th, and ²²⁶Ra isotopes and low significant correlations between the concentrations of ²³⁸U-series and ²³²Th in sand were obtained. No evidence of correlation was found between the concentrations of radioisotopes and pH, grain size, total organic matter content, bicarbonate or calcium carbonate concentrations of the sand samples. The mean values of soil-to-plant transfer factor were 0.15, 0.18, 1.52 and 0.74 for ²²⁶Ra, ²³²Th, ⁴⁰K, and ¹³⁷Cs, respectively. The range of concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K in water samples collected from five wells were<0.4–0.16,<0.4–0.13, and<0.15–1.62 Bq l^?1, respectively. The mean absorbed dose rate in outdoor air at a height of 1 m above the ground surface for the sand samples was 19.4 nGy h^?1. The Ra_eq activities of the sands are lower than the recommended maximum value of 370 Bq kg^?1 criterion limit for building materials.     

Unexpected radiation hazard in dyes of textiles

Textile dyes are among the most problematic pollutants because of their toxicity on several organisms and ecosystems. Many of the chemicals used in the textile industry may represent some health concerns. The determination of the radioactivity in textile dyes is therefore very important for both human health and environment. The study was designated to determine, for the first time, the values of ²³⁸U, ²³²Th and ⁴⁰K in nine different dyes employed in the textile industry using gamma spectrometry with a Hyper Pure Germanium (HPGe) detector. The mean activity concentrations of ²³⁸U, ²³²Th and ⁴⁰K were 29.37?±?4.48, 1.15?±?0.13 and 565?±?4 Bq/kg, respectively. The calculated radium equivalents for all samples were lower than the maximum admissible value (370 Bq/kg). The absorbed dose rates due to the natural radioactivity of the investigated samples ranged from 2.94?±?0.05 to 166?±?3 nGy/h. So, the absorbed dose rates for all samples of textile dyes were lower than the international recommended value (55 nGy/h) except the yellow dye (166?±?3 nGy/h), which recorded a significant radiological hazard. The external hazard index was also calculated. Conclusively, the results have indicated that the textile dyes may possess a measurable amount of radioactivity that should be taken into account. Therefore, safety rules and precautions should be applied for dyes used in the textile industry and for people working in this field.     

Radiation dose-dependent risk on individuals due to ingestion of uranium and radon concentration in drinking water samples of four districts of Haryana,India

Uranium gets into drinking water when the minerals containing uranium are dissolved in groundwater. Uranium and radon concentrations have been measured in drinking water samples from different water sources such as hand pumps, tube wells and bore wells at different depths from various locations of four districts (Jind, Rohtak, Panipat and Sonipat) of Haryana, India, using the LED flourimetry technique and RAD7, electronic silicon solid state detector. The uranium (²³⁸U) and radon (²²²Rn) concentrations in water samples have been found to vary from 1.07 to 40.25?µg?L^?1 with an average of 17.91?µg?L^?1 and 16.06?±?0.97 to 57.35?±?1.28?Bq?L^?1 with an average of 32.98?±?2.45?Bq?L^?1, respectively. The observed value of radon concentration in 43 samples exceeded the recommended limits of 11?Bq?L^?1 (USEPA) and all the values are within the European Commission recommended limit of 100?Bq?L^?1. The average value of uranium concentration is observed to be within the safe limit recommended by World Health Organization (WHO) and Atomic Energy Regulatory Board. The annual effective dose has also been measured in all the water samples and is found to be below the prescribed dose limit of 100?µSv?y^?1 recommended by WHO. Risk assessment of uranium in water is also calculated using life time cancer risk, life time average daily dose and hazard quotient. The high uranium concentration observed in certain areas is due to interaction of ground water with the soil formation of this region and the local subsurface geology of the region.