Natural and Artificial Radionuclides in Selected Lignites from Istanbul

The radioactivity levels of Istanbul environs lignites were determined. The gamma-spectrometric technique has been used for the determination of activity levels of naturally occurring radionuclides ^235+238U, ^228+232Th, ⁴⁰K, ²²⁶Ra and fallout radionuclides ¹³⁷Cs in lignites taken from 7 different parts of Istanbul. Concentration of ²³⁸U, ^228+232Th, ⁴⁰K, ²²⁶Ra ¹³⁷Cs and ²³⁵U were found up to 1.6 ppm, 1.7 ppm, 4.9 ppm, 56.8 Bq/kg, 34 Bq/kg, 1.8 Bq/kg, 1.6 Bq/kg, respectively. In addition total alpha- and beta-activity levels in lignite samples were found to be 7.6 and 15 eps, respectively.     

Distribution of 238U, 226Ra, 232Th and 40K in soil samples around Tarapur,India

The radioactivity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K in soil samples around Tarapur vary from 11.5 ± 2.6 to 50.3 ± 6.6, 14.9 ± 0.6 to 40.5 ± 1.2, 18.1 ± 0.4 to 75.0 ± 1.5 and 130.1 ± 1.6 to 295.1 ± 2.6 Bq/Kg respectively. The measured activity concentrations for ²³⁸U and ²²⁶Ra were compared and found in good agreement with the Indian as well as world average. The average ²³²Th and ⁴⁰K concentrations in Tarapur were lower than the Indian average value.     

Distribution and environmental impact of radionuclides in marine sediments along the Venezuelan coast

The activity concentrations of ¹³⁷Cs, ⁴⁰K, ²²⁶Ra and ²³²Th in Bq/kg from 42 marine sediment samples collected at nine sampling sites were determined in order to establish a radiological baseline along the Venezuelan coast. The radioactivity levels were determined by means of a gamma-ray spectroscopy system using a hyper-pure germanium detector in a low-background configuration. Particle size distribution and total organic matter content were also determined. Activity concentrations of ¹³⁷Cs were lower than the detection limit of the analytical technique (0.9 Bq/kg) in all studied sites. The results suggest that the variation of grain-size distribution is one of the most important factors influencing the spatial variations of ⁴⁰K, ²²⁶Ra and ²³²Th in sediments along the Venezuelan coasts. In all sampling sites, average concentrations of ⁴⁰K, ²²⁶Ra and ²³²Th were lower than the world average values. Activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in coastal marine sediments along the Venezuelan coast could be considered to be low when compared with global average values, indicating that they are not apparently above of the range that might be considered normal or background. These results suggest that the studied sites do not pose any significant radiological threat to the population. The results attained in this study should be of considerable value as baseline data and background reference levels for Venezuelan coastlines.     

Levels and effects of natural radionuclides in soil samples of Garhwal Himalaya

Distribution of natural radionuclide gives significant parameter to assess the presence of gamma radioactivity and its radiological effect in our environment. Natural radionuclides are present in the form of ²²⁶Ra, ²³²Th and ⁴⁰K in soil, rocks, water, air, and building materials. Distribution of natural radionuclides depends on the type of minerals present in the soil and rocks. For this purpose gamma spectrometer is used as tool for finding the concentration of these radionuclides. The activity concentration of naturally occurring radionuclides ²²⁶Ra, ²³²Th and ⁴⁰K in these soil samples were found to vary from of 8 ± 1 Bq/kg to 50 ± 10 Bq/kg with an average 20 Bq/kg, 7 ± 1–88 ± 16 Bq/kg with an Average 26 Bq/kg and 115 ± 18–885 ± 132 Bq/kg with an average 329 Bq/kg, respectively. In this paper, we are presenting the radiological effect due to distribution of natural radionuclide present in soil of Garhwal Himalaya.     

Assessment of radioactivity level and associated radiation exposure in topsoil from eastern region of Shangrao Prefecture,China

Natural and fallout radioactivity were estimated in topsoil samples collected in eastern region of Shangrao Prefecture, China. The average activity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K in the soil were nearly 2 times the world median value and Chinese average. The ¹³⁷Cs activity concentration decreased compared with the previously reported value in the same region. The absorbed dose rate and annual effective dose rate estimated in the study area are found to be both higher than the world average values. ²³⁸U/²²⁶Ra and ²³²Th/²²⁶Ra activity ratios were also considered in this study.

     

Study of naturally occurring radioactive material (NORM) in top soil of Punjab State from the North Western part of India

The concentration levels of ²³⁸U, ²³² Th, ⁴⁰K and ¹³⁷Cs in top soils of State of Punjab located in the North Western part of India were measured using conventional low background gamma ray spectrometric setup as well as Compton suppressed gamma ray spectrometric setup. The radioactivity level of ²³⁸U and ²³²Th was found to vary between 15 Bq/kg and 27 Bq/kg and between 16 Bq/kg and 57 Bq/kg respectively. The radioactivity level of ⁴⁰K was found to vary between 266 Bq/kg and 799 Bq/kg. The mean radioactivity level of the NORM in general was found to be similar to what is expected as a result of their normal abundance.     

Study of natural radionuclides and its radiation hazard index in Malaysian building materials

The main component of most building materials in Malaysia is rock. All rocks are known to contain natural radionuclides such as ²³⁸U and ²³²Th series as well as ⁴⁰K. In order to estimate the radiological impact to the dweller, the level of radionuclides present in various building materials available in Malaysia were analyzed using γ-spectrometry. The radiation hazard indexes were calculated based on the above results. The results showed that the activity concentration of natural radionculides ²³⁸U, ²³²Th, ⁴⁰K was between 19.0–42.2 Bq/kg, 16.5–28.8 Bq/kg and 243.3–614.2 Bq/kg, respectively. On the whole, the radionuclides concentration was still below the global average of 50 Bq/kg, 50 Bq/kg and 500 Bq/kg for ²³⁸U, ²³²Th, and ⁴⁰K, respectively The radiation hazard indexes of the building materials were also lower than the maximum value suggested.     

A device for uranium series leaching from glass fiber in HEPA filter

For the disposal of a high efficiency particulate air (HEPA) glass filter into the environment, the glass fiber should be leached to lower its radioactive concentration to the clearance level. To derive an optimum method for the removal of uranium series from a HEPA glass fiber, five methods were applied in this study. That is, chemical leaching by a 4.0?M HNO₃?C0.1?M Ce(IV) solution, chemical leaching by a 5 wt% NaOH solution, chemical leaching by a 0.5?M H₂O₂?C1.0?M Na₂CO₃ solution, chemical consecutive chemical leaching by a 4.0?M HNO₃ solution, and repeated chemical leaching by a 4.0?M HNO₃ solution were used to remove the uranium series. The residual radioactivity concentrations of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th in glass after leaching for 5?h by the 4.0?M HNO₃?C0.1?M Ce(IV) solution were 2.1, 0.3, 1.1, and 1.2?Bq/g. The residual radioactivity concentrations of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th in glass after leaching for 36?h by 4.0?M HNO₃?C0.1?M Ce(IV) solution were 76.9, 3.4, 63.7, and 71.9?Bq/g. The residual radioactivity concentrations of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th in glass after leaching for 8?h by a 0.5?M H₂O₂?C1.0?M Na₂CO₃ solution were 8.9, 0.0, 1.91, and 6.4?Bq/g. The residual radioactivity concentrations of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th in glass after consecutive leaching for 8?h by the 4.0?M HNO₃ solution were 2.08, 0.12, 1.55, and 2.0?Bq/g. The residual radioactivity concentrations of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th in glass after three repetitions of leaching for 3?h by the 4.0?M HNO₃ solution were 0.02, 0.02, 0.29, and 0.26?Bq/g. Meanwhile, the removal efficiencies of ²³⁸U, ²³⁵U, ²²⁶Ra, and ²³⁴Th from the waste solution after its precipitation?Cfiltration treatment with NaOH and alum for reuse of the 4.0?M HNO₃ waste solution were 100, 100, 93.3, and 100%.     

Terrestrial absorbed dose rate measurement in the Jhangar valley of Pakistan

Specific activity of natural radionuclides; ²²⁶Ra, ²³²Th and ⁴⁰K were measured in the agricultural soil of eastern salt range of Pakistan using gamma ray spectrometry. The soil samples were collected within the ploughing region (up to 12 cm depth) and processed before analysis. The average specific activities of different radionuclides in the dry mass of soil samples were: ⁴⁰K, (666 Bq/kg), ²²⁶Ra (51 Bq/kg), and ²³²Th (59 Bq/kg). The average outdoor terrestrial absorbed dose rate in air from gamma radiation one meter above ground surface was found to be 93 nGy/h.     

Natural radioactivity in surface marine sediments near the shore of Vizag, South East India and associated radiological risk

Naturally occurring radioactive materials were determined in surface sediments from the marine environment near the shore of Vizag in the South eastern part of India using gamma spectrometry technique. The mean activity concentration was found to be 36 ± 11, 34 ± 15, 75 ± 38 and 782 ± 223 Bq/kg and ranged from 19 to 48 Bq/kg, 11 to 57 Bq/kg, 31 to 145 Bq/kg and 363 to 1,024 Bq/kg for ²³⁸U, ²²⁶Ra, ²³²Th and ⁴⁰K, respectively. The mean radium equivalent activity, external hazard index, air absorbed gamma dose rate and annual effective dose equivalent are 203 ± 62 Bq/kg, 0.6 ± 0.2, 94 ± 27 nGy/h and 0.12 ± 0.03 mSv/year respectively. This data will serve as the baseline level for naturally occurring radionuclides in the study area and will be useful for tracking and assessing any pollution inventory in the environment of this region.     

Natural radioactivity in different commercial ceramic samples used in Yemeni buildings

In this work we calculated the radioactivity concentrations of the natural radioactive nuclides ²³⁸U, ²³²Th, ²²⁶Ra and ⁴⁰K for 10 commercial samples collected from 10 different companies which are used in the construction of Yemeni buildings. Gamma ray spectroscopy was used to analyze the samples and the concentrations of radioisotopes were determined using a hyper-pure germanium (HPGe) detector in Bq/kg dry-weight. The average concentrations of ²³⁸U, ²³²Th, ²²⁶Ra and ⁴⁰K were found to be 131.4, 83.55, 131.88 and 400.7 Bq/kg respectively. Different hazard indices were also determined. The results showed that the average radium equivalent activity (Ra_eq), the absorbed dose rate (D_r), the annual effective dose equivalent (AEDE), the external hazard index (H_ex) and representation level index (I_γ) were: 307.52 Bq/kg, 139.31 nGy/h, 1.40 mSv/yr, 0.83 and 2.15 respectively. The mean value of (Ra_eq) obtained in this study is in good agreement with that of the international value while the mean values of the other indices are found to be higher than the international reference values. The measured activity concentrations for these radionuclide were compared with the reported data obtained from similar materials used in other countries.     

Measurement of the radioactivity of238U,232Th,226Ra,137Cs and40K in soil using direct Ge(Li) γ-ray spectrometry

Radioactivity of the nuclides²³⁸U(²³⁵U),²³²Th,²²⁶Ra,¹³⁷Cs and⁴⁰K was measured in soil by direct -ray spectrometry using Ge(Li) detector. Relative laboratory method was used. Soil was dired, powdered, sieved and put into hemetically sealed container. CCRMP certified reference materials and compounds of the above nuclides mixed with fine quartz sand were used as references. Five and four -lines were used for the determination of²³²Th and²²⁶Ra, respectively, to obtain more accurate results. The most significant interferences, caused by the limited energy resolution of the detector, were resolved. In the case of ordinary soils, using one day duration of measurement and 1 kg mass of soil,²³²Th,²²⁶Ra and⁴⁰K can be determined with less than 10% relative random error. Elevated concentrations of²³⁸U(²³⁵U) and²²⁶Ra were observed in soil samples collected around a coal-fired power plant in Ajka town, Hungary.     

Natural radioactivity in soil samples of Kocaeli basin, Turkey

The city of Kocaeli is in the western part of Anatolia in Turkey and has a population of approximately 1.000.000. There is no information about radioactivity in the Kocaeli soils samples so far. For this reason, the concentrations of the natural radionuclides in soil samples from 27 different sampling stations in Kocaeli Basin and its surroundings have been determined. The results have been compared with other radioactivity measurements in different country"s soils. The typical concentrations of ¹³⁷Cs, ²³⁸U, ⁴⁰K, ²²⁶Ra, ²³²Th found in surface soil samples ranged from 2±0.6 to 25±6 Bq/kg, from 11±4 to 49±10 Bq/kg, from 161±30 to 964±127 Bq/kg, from 10±4 to 58±11 Bq/kg, and from 11±3 to 65±13 Bq/kg, respectively.     

226Ra, 228Ra and 228Ra/226Ra in surface marine sediment of Malaysia

Surface sediment samples were collected at the West (east coast and west coast of Peninsular Malaysia) and East (Sabah and Sarawak) Malaysia in several expeditions within August 2003 until June 2008 for determining the level of natural radium isotopes. Activity concentrations of ²²⁶Ra and ²²⁸Ra in surface marine sediment at 176 sampling stations were measured. The activity concentrations of both radionuclides in Malaysia (East and West Malaysia) display varied with the range from 9 to 158 Bq/kg dry wt. and 13 to 104 Bq/kg dry wt., respectively. Meanwhile, the ratio distributions of ²²⁸Ra/²²⁶Ra were ranged from 0.62 to 3.75. This indicated that the ratios were slightly high at west coast of Peninsular Malaysia compared to other regions (east coast of Peninsular Malaysia, Sabah and Sarawak). The variation of activity concentrations of ²²⁶Ra and ²²⁸Ra and its ratios were also supported by the statistical analyses of one-way ANOVA and t test at 95 % confidence level, whereby there were proved that the measured values were different between the regions. These different were strictly related to their half-life, potential input sources (included their parents, ²³⁸U and ²³²Th), parent’s characteristic, the geological setting/formation of the study area, environment origin and behavior.     

Radioactivity levels in soil of three selected sites at and around Riyadh City

In this work the naturally occurring as well as some man-made radionuclidesin soil samples have been experimentally determined to establish the backgroundradioactivity levels in three selected sites at and around Riyadh City. Concentrationsof ²³⁸U and ²³²Th radionuclides together with theirdaughter ²²⁶Ra, ⁴⁰K, ¹³⁷Cs and ¹³⁷Csin soil samples, collected from different locations in the selected siteshave been measured using a hyper-pure high-resolution germanium spectrometer.The obtained concentrations of the studied radionuclides in soil in the selectedsites are presented in tabular form in Bq/kg.     

Assessment of ingestion dose due to radioactivity in selected food matrices and water near Vizag,India

Activity concentrations of ²³⁸U, ²³²Th, ²²⁶Ra, ⁴⁰K and ¹³⁷Cs were measured in milk, egg, fruit and fish samples collected around a proposed site for setting up nuclear facilities, near Vishakhapatanam. The activity concentrations of the radionuclides ranged from 0.002 to 10.6, 0.002 to 2.8, 0.1 to 7.2, 3 to 110.8, 0.03 to 3 mBq g^?1 for ²³⁸U, ²³²Th, ²²⁶Ra, ⁴⁰K and ¹³⁷Cs considering analysed food matrices. Natural uranium was measured in drinking water samples and the values were below 15 ppb. The average ingestion dose was 2.07 ± 2.01, 2.81 ± 4.38, 7.66 ± 8.24, 1.28 ± 0.84 and 0.04 ± 0.05 μSv year^?1 for ²³⁸U, ²³²Th, ²²⁶Ra, ⁴⁰K and ¹³⁷Cs in milk, egg, fruit, fish and water. The ingestion dose received was the highest for milk, due to its high ingestion rate. It was observed that ²²⁶Ra is the largest contributor of measured radionuclides in this study for the different food matrices analysed due to its high dose conversion factor. The study was carried out as a part of baseline data generation for this region with which future changes in the radiological scenario can be compared.     

Accurate determination of naturally occurring radionuclides in Philippine coal-fired thermal power plants using inductively coupled plasma mass spectrometry and γ-spectroscopy

There is an increased interest in measuring naturally occurring radioactive materials (NORM) like coal, fly ash considering health hazards caused by naturally occurring radionuclides. This paper presents activity concentration (AC) of ²²⁶Ra, ²²⁸Ra, ²³²Th, ²³⁸U and ⁴⁰K in feed coal, bottom and fly ash samples from Philippines coal-fired thermal power plants using inductively coupled plasma mass spectrometry (ICP-MS) and high-purity germanium gamma spectroscopy (HPGe γ-spectroscopy). Coal, bottom and fly ash samples were digested using a microwave oven with a mixture of HNO₃, HClO₄ and HF. Uranium (²³⁸U) and thorium (²³²Th) ACs were also analyzed from samples using ICP-MS. A good correlation was found for the measurement of U and Th using both techniques (R² = 0.97 and 0.94 respectively). ICP-MS measurements showed the highest AC of ²³²Th and ²³⁸U in fly ash and lowest for feed coal samples. With HPGe γ-spectroscopy measurements, highest AC (in Bq kg^{− 1}) of ²²⁶Ra, ²²⁸Ra, ²²⁸Th and ⁴⁰K, were noticed in fly ash followed by bottom ash and feed coal. ICP-MS method is rapid for the measurement of uranium and thorium in comparison to γ-spectroscopy as secular equilibrium is not required. Activity concentrations of bottom and fly ash samples were found to be within the reported values worldwide and below the International Atomic Energy Agency recommended values for regulatory control.     

Radionuclide activities and elemental concentrations in sediments from a polluted marine environment (Saronikos Gulf-Greece)

The levels and depth distributions of the natural radionuclides ²³⁸U, ²³²Th, ²²⁶Ra, ⁴⁰K and the man-made ¹³⁷Cs were analyzed by γ-ray spectrometry, while the concentrations of 26 chemical elements were measured by INAA in sediment samples collected from the organic mud layer that covers the Keratsini–Psitalia strait, Saronikos gulf (Greece). The average activity concentration values of ²²⁶Ra, ²³²Th and ⁴⁰K were lower when compared, whereas that of ²³⁸U was comparable to the average Greek and world values. The elemental contamination of the sediments was estimated on the basis of the calculated EF values. The results revealed high EF values of As, Br, Cr, Ni, Sb, Se, Zn ranging from 160 for Br to 10 for Cr, whose main sources are probable related to contaminated sewage outfall from the area of Athens and the Piraeus Harbour.

     

Spatial distribution and risk assessment of radioactivity and heavy metal levels of sediment,surface water and fish samples from Lake Van,Turkey

In this study, radioactivity levels of 228 lake water samples, 63 upper and depth sediment samples and 12 fish samples from Lake Van were investigated from 2005 to 2008 and the distribution patterns of the radionuclides were presented. Analysis included gross alpha–beta and total radium isotopes activities and uranium concentrations of the water, and gross alpha and gross beta activities and relevant ²³⁸U, ²³²Th and ⁴⁰K activity of the sediment and fish samples of the lake. Mean gross alpha, gross beta and radium isotopes activities of lake water were found 0.74 ± 0.46, 0.02 ± 0.01 and 0.06 ± 0.04 Bq/L, respectively. Mean gross alpha and beta activities in upper and depth sediments were found to be 41 ± 6 and 1,514 ± 74 Bq/kg; 77 ± 5 and 394 ± 24 Bq/kg at a 95 % confidence level, respectively. Mean activities of ²³⁸U, ²³²Th and ⁴⁰K activity concentrations in upper and depth sediments were determined to be 225 ± 22, 70 ± 7 and 486 ± 39 Bq/kg; 174 ± 4, 63 ± 3 and 263 ± 25 Bq/kg, respectively. The mean gross alpha and beta, ²³⁸U, ²³²Th and ⁴⁰K aktivities in fish samples were established as 47 ± 18, 470 ± 12, 0.57 ± 0.220, 0.022 ± 0.006, 319 ± 11 Bq/kg, respectively. The transfer factor from lake water to fish tissues, annual intake by humans consuming fish, and annual committed effective doses were estimated and evaluated.     

Radiochemical determination of uranium and radium isotope in natural water using liquid scintillation counter

²³⁴U, ²³⁸U, ²²⁶Ra, and ²²⁸Ra were analyzed in 14 Korean hot spring waters. Uranium was extracted with mixture of extractive scintillation cocktail containing HDEHP and ²³⁴U, ²³⁸U were analyzed with LSC. Radium isotopes were separated using Ba coprecipitation method and counted with LSC and ²²⁸Ra was also analyzed its daughter ²²⁸Ac with HPGe γ-detector. Among them ²²⁶Ra was ranged <0.01–0.155 Bq/L and ²²⁸Ra is below detection limit <0.1 Bq/L. And also, uranium content was ranged <0.01–49.7 μg/L and ²³⁴U/²³⁸U ratio was ranged 0.69–1.17.