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1.
Summary Radon measurements were carried out in a Japanese wooden house built on granitic geology, where radon-rich well water is used. Atmospheric radon concentrations were measured over one year with passive integrated radon monitors. The monitors were distributed at several locations in the house and were replaced every two months. In order to confirm the diurnal variation and heterogeneous distribution of radon, short-term measurements were carried out accordingly. Radon, its decay products and terrestrial gamma-radiations were measured in this survey. From the long-term measurement, the radon concentration in the house ranged from 14 to 184 Bq. m-3with an arithmetic mean of 45 Bq. m-3. A radon concentration of 184 Bq. m-3was observed in the bathroom in spring (March-May) though the radon level was normal in the living room and bedroom. In order to characterize the house, similar measurements were conducted in several surrounding houses. There was a significant difference in radon concentration between the investigated houses. There was a spatial distribution of the radon concentration and the highest value was found in the bathroom. Radon and its decay products concentrations varied with time, which increased from midnight to morning whereas they decreased during daytime. Although the radon concentration in tap water was 1 Bq. l-1, a high level of 353 Bq. l-1was found in the well water.While well water was being used, the indoor radon concentration near the bathroom increased rapidly with a maximum value of 964 Bq. m-3. It is clear that the use of well water enhanced the radon level around the bathroom.  相似文献   

2.
In order to evaluate the possible radiological impact to the local public and environment from a phosphogypsum stockpile, 210Po and 210Pb concentrations in river water, lagoon water, suspended matter, superficial sediment, algae and bivalves samples collected in Venice lagoon area have been investigated. The results show that the mean 210Po and 210Pb concentrations in river water are 1.42±0.36 mBq.l-1 and 1.46±0.39 mBq.l-1 with a mean 210Po/210Pb ratio of 0.98±0.17 and about 60% of them are associated with the particulate; 210Po and 210Pb contribution from the phosphogypsum stockpile to the river water is negligible. Higher 210Po (2.61-5.67 mBq.l-1) and 210Pb (1.31-3.62 mBq.l-1) concentrations in the lagoon waters have been observed if compared with the literature values. About 60% of 210Po and 210Pb are found in the soluble form with a mean 210Po/210Pb ratio of 1.79±1.47. 210Po and 210Pb concentrations in 28 out 37 sediment samples ranged from 26 to 45 Bq.kg-1 (dry weight), only 9 sediments with 210Po and 210Pb concentrations greater than 45 Bq.kg-1 are found and most of them are located 1-4 km near the phosphogypsum stockpile. The elevated 210Po and 210Pb concentrations in the sediments may be due to the contamination from the phosphogypsum stockpile. The mean 210Po/210Pb ratio (0.986±0.049) in the sediments shows that 210Po and 210Pb exist in nearly secular equilibrium. 210Po and 210Pb concentrations in algae vary with different species. The mean 210Po and 210Pb concentrations in Gracilaria compress and Ulva laetevirens which show a similar behavior, are 3.18±1.23 Bq.kg-1 and 2.42±1.26 Bq.kg-1 (fresh weight), respectively, with a mean 210Po/210Pb ratio of 1.45±0.34. The mean concentration factors with respect to the filtered water are 1096±424 for 210Po and 1299±680 for 210Pb. The mean 210Po and 210Pb concentrations in the soft part of Mytilus edulis are 23.2±9.7 Bq.kg-1 and 0.537±0.203 Bq.kg-1 (fresh weight), respectively, with a mean 210Po/210Pb ratio of 43.6±10.0. The mean concentration factors with respect to the filtered water are 8006±3351 for 210Po and 290±109 for 210Pb, showing a very high accumulation effect for 210Po. The accumulation behaviors of Cerastoderma glaucum and Tapes philippinarum for 210Po are similar to Mytilus edulis, but that for 210Pb seems less effective, corresponding to a relatively higher 210Po/210Pb ratio. The estimated committed effective doses from 210Po for the individual local public through ingestion of bivalves are in the range of 0.050-0.231 mSv.y-1.  相似文献   

3.
Gross-alpha and gross-beta activities of fourteen taps and wells, four lakes and three drinking water supplies in Elazi (Turkey) were determined. The results obtained indicate that although the natural radioactivity of six tap, two drinking, four lake and three well water samples does not exceed the requirements of the World Health Organisation (WHO) guidelines, however, most of them do exceed those of the Institution of Turkish Standards (ITS). Concentrations ranging from 0.02 to 0.17 Bq.l-1 and from 0.01 to 0.29 Bq.l-1 for gross-alpha and gross-beta radioactivity, respectively, were observed in all samples. For most of the samples, there were no regular correspondence between gross-alpha and gross-beta activity concentrations.  相似文献   

4.
A new and accurate method for the determination of uranium isotopes (238U, 234U and 235U) in environmental samples by alpha-spectrometry has been developed. Uranium is preconcentrated from filtered water samples by coprecipitation with iron(III) hydroxide at pH 9-10 using an ammonia solution and the precipitate is dissolved in HNO3 and mineralized with H2O2 and HF; uranium in biological samples is ashed at 600 °C, leached with Na2CO3 solution and mineralised with HNO3, HF and H2O2; uranium in soil samples is fused with Na2CO3 and Na2O2 at 600 °C and leached with HCl, HNO3 and HF. The mineralized or leaching solution in 2M HNO3 is passed through a Microthene-TOPO (tri-octyl-phosphine oxide) column; after washing, uranium is directly eluted into a cell with ammonium oxalate solution, electrodeposited on a stainless steel disk and measured by alpha-spectrometry. The lower limits of detection of the method is 0.37 Bq.kg-1 (soil) and 0.22 mBq.l-1 (water) for 238U and 234U and 0.038 Bq.kg-1 (soil) and 0.022 mBq.l-1 (water) for 235U if 0.5 g of soil and 1 litre of water are analyzed. Five reference materials supplied by the IAEA have been analyzed and reliable results are obtained. Sample analyses show that, the 238U, 234U and 235U concentrations are in the ranges of 0.30-103, 0.49-135 and 0.02-4.82 mBq.l-1 in waters, of 1.01-7.14, 0.85-7.69 and 0.04-0.32 Bq.kg-1 in mosses and lichens, and of 25.6-53.1, 26.4-53.8 and 1.18-2.48 Bq.kg-1 in sediments. The average uranium yields for waters, mosses, lichens and sediments are 74.5±9.0%, 80.5±8.3%, 77.8±4.9% and 89.4±9.7%, respectively.  相似文献   

5.
Summary The gross alpha- gross beta-activity, 137Cs and 90Sr in the water and sediment samples taken from the Keban Dam Lake, Uluova Region, was investigated in 2003 and 2004. We have found that in spring the concentration of 137Cs in the surface water and deep sediment changed between 0.001-0.01 Bq/l (0.4-2.5 Bq.kg-1) that of 90Sr between 0.0001-0.009 Bq/l (0.1-9 Bq.kg-1) and in autumn the values were 0.0001-0.009 Bq/l (0.4-8 Bq.kg-1) for 137Cs and 0.0002-0.005 Bq/l (0.6-4 Bq.kg-1) for 90Sr, respectively. The results were presented in form of iso-curves.  相似文献   

6.
Summary One of the high-level natural radiation areas (HLNRAs) in Iran is located in the south of Iran in the Hormozgan province. Uranium and its daughters, such as radium and thorium cause areas of elevated natural radiation. An unknown hypothermal mineral and radioactive spring was discovered containing high-level radiation, 42 mSv . y-1 maximum effective dose around spring was measured. 40K, 226Ra and 232Th radionuclides were detected with the maximum activity of 11.80 Bq . l-1, 3.48 Bq . l-1 and 2.52 Bq . l-1, respectively. These activities are the second highest in comparison to those in the Ramsar radioactive springs, especially Ab-e-siah spring, which contains 146.5 Bq . l-1 activity. Ocillatoria spp., Lyngbya spp. and a kind of ciliatawere observed in this spring. The results showed that the radioactive spring falls into the sodium chloride category.  相似文献   

7.
Summary A reconnaissance study has been made on the distribution of 238U, 232 Th, 40K, 137Cs and geochemical features in soil and sediment samples at various locations in the coast of Persian Gulf. Activity concentration levels due to radionuclides were measured in 50 samples of soils and sediments collected from the coast of Hormozgan. From the measured spectra, activity concentrations were determined for 40K (range from 140 to 1172 Bq . kg-1), 137Cs (from 0 to 15 Bq . kg-1), 238 U (from 29 to 385 Bq . kg-1) and 2321 Th (from 9 to 156 Bq . kg-1) with the lowest limit of detection (LLD) of 68, 3.2, 4.3 and 4.3 Bq . kg-1, respectively. The dose rate from ambient air at the soil ranges was between 23 to 177 nGy . h-1 with an average of 60±7.86 nGy . h-1.  相似文献   

8.
We investigated the distribution of aquatic plants and the absorption of radionuclides by them in the brackish Lake Obuchi, Japan, which is bordered by nuclear fuel cycle facilities. We studied 5 species of submerged plants: Zannichellia palustris, Ruppia maritima, Potamogeton pectinatus, Zostera japonica, and Z. marina. The plants contained many elements, including radionuclides. The concentrations of 238U, 137Cs, and 90Sr in Z. marina were 11.3-12.4, 0.000-0.144, and 0.151-0.202 Bq.kg-1 dw, respectively. Those in Z. japonica were 5.2-8.8, 0.000-0.267, and 0.081-0.175 Bq.kg-1 dw, respectively. The concentrations of these radionuclides in the plants tended to be higher in higher-salinity regions than in lower-salinity regions of the lake. We found a close relationship between photosynthetic activity and the absorption of stable Sr by plants in the laboratory. Salinity, illumination, and water temperature influenced the photosynthetic activity of the plants and the consequent absorption of elements.  相似文献   

9.
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%.  相似文献   

10.
Natural radioactivity in the aquatic media has been determined by collecting samples of river, stream and drinking water from the northwestern areas of Pakistan. The concentrations of 40K, 226Ra and 232Th have been measured using a low background gamma-spectrometer and a 10 cm3 planar intrinsic high purity germanium detector. The annual ingestion of these radionuclides, using local consumption rates (average over the whole population) of 0.9 l.d-1, were estimated to be 49.2, 6.2 and 1.1 Bq.y-1 for 40K, 226Ra and 232Th, respectively. A comparison of the annual intakes of these radionuclides, using annual consumption rates of NCRP, ICRP and FBSP shows that the contribution from natural radionuclides to annual intake is slightly greater for NCRP than for ICRP and FBSP consumption rates. However, the estimated values and weighted means of these radionuclides compare well with the world average. The annual effective dose equivalent from drinking water was found to be 3.6.10-6 mSv.y-1 (226Ra), 3.2.10-12 mSv.y-1 (232Th) and 2.1.10-6 mSv.y-1 (40K). These values are lower than those given by NCRP.  相似文献   

11.
Natural radioactivity in various types of marbles available in Rawalpindi/Islamabad industrial area have been assessed using HP(Ge) gamma-ray spectrometer. The concentration of 40K, 226Ra and 232Th ranges from 6.15 to 159.65 Bq.kg-1, 1.45 to 29.34 Bq.kg-1 and 1.16 to 6.28 Bq.kg-1, respectively. The radium equivalent activity lies between 5.56 to 33.42 Bq.kg-1. The average external and internal indices have been found to be 0.03 and 0.05, respectively. The average absorbed dose rate at 1 m was found to be 6.53 nGy.h-1. The estimated annual effective dose rate for whole body was found to be 0.04 mSv.y-1. These values are smaller than those predicted by UNSCEAR for normal background areas. The marbles analyzed pose less health hazard as compared to Pakistani baked bricks and other construction materials.  相似文献   

12.
Summary A systematic study of natural and fall-out radionuclides was carried out with the environmental samples of soil, vegetation and water from some regions of North West Frontier Province (NWFP) of Pakistan. The pretreatment of the samples was performed in the laboratory using IAEA recommended methods. The analysis of gamma-emitters such as 40K, 226Ra, 232 Th and 137Cs was performed with a high purity germanium detector (HPGe). For the determination of 90Sr, a liquid scintillation counting system was used. The average specific activities of 40K, 226Ra, 232 Th and 137Cs have been found to be 307±101 Bq . kg-1, 10.2±3 Bq . kg-1, 24±6 Bq . kg-1 and 2.8±1.3 Bq . kg-1, respectively, in soil samples. Vegetation samples have smaller values of specific activities and even the analysis of water samples showed values less than LLD for earlier reported radionuclides. Other parameters like hazard indices, radium equivalent activities, absorbed dose rates and effective dose equivalents have also been determined. All these parameters have values less than their respective limiting values representing that the surveyed areas have no significant hazard from health point of view. Analysis of 90Sr for all the samples showed results below LLD. The present study provides a general background of the detectable radionuclides for the surveyed areas that will be helpful in any radiological emergency.  相似文献   

13.
Summary Due to the widespread use of granites as building and ornamental materials, measurements of 226Ra, 232Th and 40K activities in commercial granites have been carried out using a NaI(Tl)g-ray spectrometer with a matrix-inversion-based spectral stripping technique. The concentrations of 226Ra, 232Th and 40K in Chinese commercial granite range from 14.5 to 204.7 Bq. kg-1, 16.7 to 186.7 Bq. kg-1and 185.7 to 1745.6 Bq. kg-1, respectively. The mean values of the activity concentrations of 226Ra, 232Th and 40K in red and pink commercial granites are all higher than those in black and gray commercial ones. The radium equivalent activity (Raeq), the external hazard index (Hex), the internal hazard index (Hin ) and the annual gonadal dose equivalent (AGDE) were also calculated and compared to the international recommended values. Six types of red commercial granites (CBR, MLR, QXR, PBR, JXR, LQR, YDR and TSR) of China do not satisfy the universal standards.  相似文献   

14.
Sea surface microlayer (SML) and sea water samples (SSW) collected in the Gerlache Inlet Sea (Antarctica) were analysed for n-alkanes and polycyclic aromatic hydrocarbons (PAHs). The SML is a potential enrichment site of hydrophobic organic compounds compared to the underlying water column. Total concentration ranges of n-alkanes and PAHs (dissolved and particulate) in subsurface water (− 0.5 m depth) were 272-553 ng l− 1 (mean: 448 ng l− 1) and 5.27-9.43 ng l− 1 (mean: 7.06 ng l− 1), respectively. In the SML, the concentration ranges of n-alkanes and PAHs were 353-968 ng l− 1 (mean: 611 ng l− 1) and 7.32-23.94 ng l− 1 (mean: 13.22 ng l− 1), respectively. To evaluate possible PAH contamination sources, specific PAH ratios were calculated. The ratios reflected a predominant petrogenic input. A characterisation of surface active substances was also performed on SML and SSW samples, both by gas bubble extraction, and by dynamic surface tension measurements. Results showed a good correlation between n-alkanes, PAHs and refractory organic matter.  相似文献   

15.
Summary Seventy nine samples, including soil and rock, were collected from the agrestic region of the State of Pernambuco, Brazil. The activity concentrations of 238U and 226Ra in the samples were determined by gamma-spectrometry using an HPGe detector. The concentrations of 238U were 22 Bq . kg-1 to 22 kBq . kg-1. The concentrations of 226Ra were 14 Bq . kg-1 to 17 kBq . kg-1. The 238U/226Ra ratios in the soil were 0.7 to 3.4 (arithmetic mean 1.7). The radiometric data were evaluated to explain 238U and 226Ra migration in the soil and the possible consequences to the environment.  相似文献   

16.
There are two types of lakes in the vicinity of the nuclear fuel cycle facilities in Rokkasho-mura. One is a brackish lake, Obuchinuma Lake, and the other is a freshwater lake, Takahokonuma Lake. Tritium concentrations in Obuchinuma Lake had a good negative correlation with salinity at any sampling point and period. We consider that the water of Obuchinuma Lake has been only slightly influenced by precipitation depending on the ratio of seawater and river water of the Futamata River. Tritium concentrations in Takahokonuma Lake ranged from 0.6 to 1.5 Bq·1-1, and were higher than that in precipitation in Rokkasho-mura. Tritium concentration in rivers flowing into the lakes ranged from 0.7 to 2 Bq·l-1, and were higher than that in the precipitation. It is assumed that ground waters with higher levels of tritium inflow into the rivers.  相似文献   

17.
Summary A survey was carried out to determine radioactivity concentrations and associated dose rates from the naturally occurring nuclides 232 Th, 238U and 40K in various surface soil formations of Alhkraje city. Samples were collected from different areas of the study, sieved through a fine mesh, sealed in 0.5-liter plastic Marinelli beaker, and measured in the laboratory for 24 hours each. From the measured g-ray spectra, radioactivity concentrations were determined for 232 Th ranging from 5.32±2.59 to 16.40±2.04 Bq . kg-1, 238U (2.87±0.18 to 18.83±0.81 Bq . kg-1), 40K (211.33±55.04 to 378.97±36.46 Bq . kg-1) and 137Cs (0 to 3.19±1.02 Bq . kg-1). Absorbed dose rates in air doors were calculated to be in the range of 15.29±2.65 to 30.00±3.24 nGy . h-1, the corresponding effective dose rates per person outdoors were estimated to be between 21.00±0.95 to 36.83±2.11 mSν. y-1, assuming a 20% occupancy factor.  相似文献   

18.
Polonium-210 was determined in 34 kinds of imported tea and 9 kinds of maté collected from the Syrian local market. The 210Po concentration was found to vary from 5.5 to 39 Bq.kg-1 and 47 to 82 Bq.kg-1 in tea and maté samples, respectively. In addition 210Po was also determined in tea and maté infusions where different infusion conditions have been examined: amount, temperature and infusion time. The results have shown that the amount of 210Po transferred from tea and maté leaves to the aqueous extract ranged from 9 to 21% and 3 to 15%, respectively. The annual intake of 210Po by Syrians due to tea consumption and maté infusions was calculated and found to be 9 Bq and 151 Bq for tea and maté, respectively: washing of maté with warm water is recommended before preparation the infusions to decrease the annual intake of 210Po. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

19.
Summary Radionuclide (137Cs, 238U, 232Th and 40K) concentrations were determined in a sediment trap and bottom sediment samples collected from a station at the eastern Turkish coast of the Black Sea. The specific activity of the 137Cs radionuclide in the settling particles ranged from 0.04±0.01 to 0.10±0.02 Bq. g-1dry weight. The calculated flux rate of the 137Cs was between 0.37 and 2.59 Bq. m-2. d-1in the sampling periods of 2002 and 2003. The 137Cs concentration in the bottom sediment profile were between 0.039±0.013-9.083±0.017 Bq. g-1dry weight in the same station. The vertical profile of the radionuclides suggests that they have little mobility during the 17 years after the Chernobyl accident.  相似文献   

20.
Summary Main sources of radionuclides in steel in nuclear decommissioning are the unintentional melting of orphan sources and scrap. This paper presents data about the activity of γ-emitters in German steels obtained by low-level γ -ray spectrometry in an underground laboratory. The 60Co activity exceeds only 2% of the 215 analyzed samples with a detection limit of 4.4 . 10-5 Bq . g-1. Even the maximum measured 60Co activity of 2.5 . 10-4 Bq . g-1 is a factor of 400 lower than the clearance level. The determination of the detector efficiency is also described for these unusual samples using Monte Carlo calculations.  相似文献   

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