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1.
Liquid scintillation counting (LSC) and pulse shape analysis (PSA) was used in measuring radon and gross alpha- and beta-activities in groundwater. We used conventional LSC counters for the measurement of radon in water, but low-background LSC spectrometers for the gross activity measurements. The lower limit of detection (LLD) for radon in water is 0.6 Bq/l for a 60 min count with a conventional counter, but 0.1 or 0.2 Bq/l, with the two types of low-background LSC spectrometers equipped with a pulse shape analyser (PSA). The gross alpha and beta activity measurements are made using a simple sample preparation method, PSA of a low background LSC and spectrum analysis. The LLD recorded for gross alpha and beta with the two spectrometers are 0.02 and 0.03 Bq/l and 0.2 and 0.4 Bq/l, respectively, for a 180 minutes count and a 38 ml sample volume. The method also enable the calculation of the U and226Ra contents in water and indicates the presence of some other long-lived radionuclides (210Pb,228Ra or40K). The LLD for U recorded with both spectrometers is 0.02 Bq–1 and for226Ra 0.01 Bq·1–1. The LLDs attained by this LSC method are two orders of magnitude lower than the maximum permissible concentrations set for U and226Ra.  相似文献   

2.
Summary It is well known that the interest in radon concentration indoor as a pollutant emerged during the energy crisis of seventies which led to reduce ventilation in dwellings. Recently the Euratom Recommendation 2001/928 suggested the necessity of performing frequent 222Rn checks on tap waters. As a consequence of this Recommendation, Urbino and Perugia Universities carried out a preliminary 222Rn determination on tap waters of the Pesaro-Urbino province. Samplings were carried out in twenty-eight sites and radon concentration was determined by liquid scintillation counting and gamma-spectrometry. The results obtained by the two techniques were comparable (the deviation from the mean is lower than 10% for 54.5% of the samples). The resulted 222Rn concentration was very low (5 Bq . l-1 for 43% of the samples) and, therefore, radon in waters cannot be considered as a direct radiological risk for the local population.  相似文献   

3.
A method in which222Rn is extracted from 0.5 1 water samples to 20 ml toluene is described. 10 ml toluene solution with extracted222Rn is directly added to a glass scintillation vial containing 10 ml of liquid naphthalene based scintillation cocktail. Apart from diluting by toluene, the final counting solution still has excellent properties in terms of: / separation by pulse shape analysis, detection efficiency and background in the -region. The detection limit of222Rn for 0.5 1 water samples was 1.5 mBq l–1 (for 12,000 s count time). The concentration of222Rn in different environmental samples such as rain, tap and mineral waters as well as deep well waters were determined.  相似文献   

4.
Radon-222 (Rn) has universally been found in well water. Non-stagnant ground water is collected at the well head while the well is pumping. The water is adjusted to a slow, non-aerated, steady flow through a clear tube, and a 500 ml glass bottle is filled. The sample is tightly capped after a high meniscus has developed. In the laboratory, standard 22 ml glass vials are filled with 10 ml of a toluene based mineral oil LS cocktail. Then, two 5 ml sample aliquots are pipetted into the vial. Vials are capped tightly, shaken vigorously, and placed in the liquid scintillation (LS) counter. Secular equilibrium is established in approximately 4 hours, after which samples are counted for 100 minutes each. The counting efficiency for Rn and progeny ranges between 315 to 345 percent depending on the chosen spectral window. The average background is about 6 cpm. A total of 28 wells were tested for Rn in the Carefree-Cave Creek, Arizona, USA area. The area's geometric average Rn concentration was found to be 46.5 Bq·l–1. The associated estimated lung dose is 0.51 mSv·y–1.Deceased 1 June 1991.  相似文献   

5.
A procedure for the determination of 222Rn in environmental water samples using liquid scintillation counting (LSC) was applied. The extractive scintillator RADONSÒ and an ultra-low background 1220 QuantulusÔ were used. A minimum detectable activity of 0.1 Bq·l?1 in 20 ml was found with low-diffusion polyethylene vials and 200 minute measurement time. Quenching effects and possible interferences due to the existence of other radionuclides in the extraction process were studied. The procedure was controlled by gamma-ray spectrometry of the 222Rn daughters. Applications to environmental samples collected from spas, wells, and public springs in Extremadura (Spain) are presented.  相似文献   

6.
7.
A comparison between the counting parameters of solid and liquid scintillation methods for radon determination in water is attempted. The counting efficiency is better for a toluene-based liquid scintillator but, as the background is considerably higher than in solid scintillators, the figure of merit and the lower limit of the measurable activity are favorable for a scintillation counter based on zinc sulfide (Ag activated) scintillator.  相似文献   

8.
The indoor 222Rn radionuclide was directly absorbed in typical 20 ml glass scintillation vials by passing ?3 dm3 of ambient air through 16 ml of water-immiscible non-volataile scintillation cocktail Ultima-Gold F for 10 min. The activity of radon and its two α-emitting daughters: 218Po and 214Po, was determined with the BetaScout low-background liquid scintillation counter. The limit of 222Rn detection is 9 Bq/m3, and the quantification limit with 20% relative accuracy is 28 Bq/m3. The results of the indoor Rn measurement in different houses showed good consistency with results obtained from a Sarad EQF 3220 device.  相似文献   

9.
10.
Possibilities of the method based on both the selective separation of radioiodine from milk using anion-exchange resin as well as the131I counting in heterogeneous mixture of this anex with a liquid scintillator are presented. For samples of 4 dm3 volumes, the separation and counting efficiencies about 78% and 45% are achieved. Under the same experimental conditions the background rate is about 0.25 CPS /15 CPM/ and the LLD corresponds to about 7 mBq.dm–3 /0.2 pCi. dm–3/.  相似文献   

11.
Summary A method for the determination of low-level radium isotopes in mineral and environmental water samples by alpha-spectrometry has been developed. Radium-225, which is in equilibrium with its mother 229Th, was used as a yield tracer. Radium were preconcentrated from water samples by coprecipitation with BaSO4and iron (III) hydroxide at pH 8-9 using ammonia solution, then isolated from uranium, thorium and iron using a Microthene-TOPO chromatography column at 8M HCl, separated from barium in a cation-exchange resin column using 0.05M 1,2-cyclohexylenedinitrilotetraacetic acid monohydrate at pH 8.5 as an eluant, and finally electrodeposited on a stainless steel disc in a medium of 0.17M (NH4)2C2O4at pH 2.6 and current density of 400 mA. cm-2, and counted bya-spectrometry. Optimum experimental conditions for radium separation, purification and electrodeposition have been studied and discussed in the paper. The lower limits of detection of the method are 0.11 mBq. l-1for 226Ra, 228Ra and 224Ra, respectively, if 2 l of water are analyzed. The method has been checked with a certified reference material IAEA-Soil-6 supplied by the International Atomic Energy Agency and reliable results were obtained. Eighteen water samples collected in Italy have been analyzed with the method, the mean radiochemical yields for radium were 86.2±6.5%. The obtained radium concentrations were in the range of 0.50-60.8 mBq. l-1for 226Ra, of 0.10-25.7 mBq. l-1for 228Ra, and of£LLD-7.97 mBq. l-1for 224Ra. The 228Ra/226Ra and 224Ra/226Ra ratios were in the range of 0.189-4.45 and£LLD-0.941, respectively.  相似文献   

12.
The concentrations and distributions of natural radioactivity, uranium and radon in lake waters from around Van, Turkey were investigated with an aim of evaluating the environmental radioactivity. Fourteen lake waters were collected from different six lakes around Van (Turkey) to determine 238U, 222Rn and total alpha and total beta distributions in 2009. The total α and total β activities were counted by using α/β counter of the multi-detector low background system (PIC-MPC-9604) and the 238U concentrations were determined by inductively coupled plasma-mass spectrometry (Thermo Scientific Element 2) and radon concentrations were measured with the solid state nuclear track detector technique. The activity concentrations ranging from ND to 0.039 Bq L?1 and from 0.026 to 3.728 Bq L?1 for total alpha and beta, respectively, and uranium concentrations ranging from 0.083 to 3.078 μg L?1, and radon concentrations varying between 47.80 and 354.86 Bq m?3 were observed in the lake waters.  相似文献   

13.
This paper presents a method for the determination of radium isotopes in mineralised mine waters, based on the separation of alpha- and beta-intensities measured in the precipitate by a liquid scintillation spectrometer in two time intervals (1 day and 7 days) after radium precipitation. The count rates of -particles give not only the concentration of alpha emitters (226Ra and224Ra), but also make possible to find the -counting efficiency of the system and through that-to determine the concentration of the -emitting radium isotope (228Ra) with higher accuracy. An improved chemical procedure was elaborated. By this method radium isotopes in different water samples were determined, in wide range of concentrations, from about 0.06 Bq/dm3 in potable water to more than 100 Bq/dm3 in some mine brines. As an example some analytical results are given. The detection limit, defined as three standard deviations, is-for both radium isotopes –0.03 Bq/dm3 (for intial volume of water sample equal to about 1 dm3 and for counting time of each measurement not longer than 1 hour).  相似文献   

14.
A simple method for rapid determination of131I in soil is described. The method is based on the specific separation and concentration of radioiodine from the soil extract with a liquid anion exchanger and measuring its radioactivity with liquid scintillation counting. The131I from soil is extracted with aqueous solution of sodium hydroxide. The method permits the determination of131I with a lower limit of detection less than 0.1 Bq/10 g of soil.  相似文献   

15.
The lack of a suitable tracer has severely limited the use of radioisotope tracer experiments in environmental and biological studies on aluminium. The only aluminium radioisotope with a half-life greater than 10 min is the long-lived positron emitter 26Al (t1/2 7.2 x 10(5) years). The exposure of this nuclide and the difficulty in attaining sufficiently low determination limits with standard radioanalytical techniques have restricted its application as a radioactive tracer. The development of a simple method for the routine determination of 26Al using Cerenkov counting and a Quantalus 1220 low-level liquid scintillation spectrometer is reported. For a 300 min counting time, determination limits of about 60 mBq in water samples and 120 mBq in biological (fish gill) samples can be attained. With these levels of determination, the use of 26Al as a tracer is a viable technique for the study of aluminium in environmental and biological systems.  相似文献   

16.
The concentration of radon (222Rn) was measured in the soil near the ground surface, using CR/39 solid state nuclear track detectors. The measurements were carried out in PVC tubes at 0.25 m intervals up to 1.25 m. The detectors were etched in 7N NaOH solutions at 80°C. The -tracks from radon's decay were counted using a microscope. A microscope-camera-computer system developed for automatic counting was also used. The results provide evidence for the non-diffusive transport of radon in soils. A transport length of (46.9±3.2) cm was estimated for radon transport near ground surface. Also the variation of soil's radon concentration was correlate to humidity and atmospheric pressure.  相似文献   

17.
In the present study, the deposition velocities of 222Rn/220Rn decay products were measured experimentally using SSNTD based passive detectors, direct radon progeny sensor (DRPS) and direct thoron progeny sensor (DTPS) and the results were compared with obtained values by Monte-Carlo simulations. In both cases, deposition velocities were found to be log-normally distributed and also the experimentally measured geometric mean (GM) and geometric standard deviation (GSD) of (0.12, 1.85) m h?1 for radon decay products and (0.07, 1.75) m h?1 for thoron decay products were found to be in good agreement with the simulated values.  相似文献   

18.
Feng  Xixi  Han  Qiao  Wang  Mingya  Mao  Pan  Sun  Ang  Zhang  Chunhui  Chen  Chun  Wang  Mingshi 《Journal of Radioanalytical and Nuclear Chemistry》2021,330(3):883-890
Journal of Radioanalytical and Nuclear Chemistry - The exhalation of radon from waters surrounding active fault zones is at present not well understood. In this work, radon concentrations in urban...  相似文献   

19.
Journal of Radioanalytical and Nuclear Chemistry - A method was applied in the separation and determination of trace lithium in uranium products. Separation and enrichment of lithium was carried...  相似文献   

20.
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