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1.
This study of environmental radioactivity was carried out in the soils of an urban area. Naturally occurring gamma-emitting radionuclides and man-made 137Cs were found in the soil profiles collected from four parks in the central Belgrade city area and the soil layer was examined every 10 cm and to a depth of 50 cm. Radioisotope activity concentrations (Bq kg?1) in the samples of urban soil using the gamma-ray spectrometry method were in the range of 14–46 for 238U, 33–50 for 226Ra, 29–63 for 210Pb, 1.2–3.4 for 235U, 28–50 for 232Th, 424–576 for 40K and 0.7–35.8 for 137Cs. Some of the basic physicochemical soil properties (pH, organic matter content, calcium-carbonate content, particle size distribution) were determined to investigate the impact on the vertical distribution of radionuclides. The results of this investigation showed that variations of activity concentration ratios of radionuclides that belong to the same (238U/226Ra) or different radioactive series (232Th/226Ra; 235U/238U), including 210Pb/137Cs ratios could well be explained by the properties of the soil. Alkaline pH reaction, the accumulation of organic matter in the uppermost and of carbonates in the deepest layers of urban soil had an effect on 238U/226Ra, and 210Pb/137Cs activity concentration ratio values, while 232Th/226Ra and partially 235U/238U ratios were associated with the particle sizes vertical distribution. A study of radionuclides in the samples of leaves of two deciduous tree species common for these parks was also conducted and 210Pb and 40K were found concentrated in leaves rather than other investigated radionuclides.  相似文献   

2.
Factors controlling the groundwater transport of U, Th, Ra, and Rn   总被引：1，自引：0，他引：1  
A model for the groundwater transport of naturally occurring U, Th, Ra, and Rn nuclides in the238U and232Th decay series is discussed. The model developed here takes into account transport by advection and the physico-chemical processes of weathering, decay, α-recoil, and sorption at the water-rock interface. It describes the evolution along a flowline of the activities of the238U and232Th decay series nuclides in groundwater. Simple sets of relationships governing the activities of the various species in solution are derived, and these can be used both to calculate effective retardation factors and to interpret groundwater data. For the activities of each nuclide, a general solution to the transport equation has been obtained, which shows that the activities reach a constant value after a distance ϰi, characteristic of each nuclide. Where ϰi is much longer than the aquifer length, (for238U,234U, and232Th), the activities grow linearly with distance. Where gKi is short compared to the aquifer length, (for234Th,230Th,228Th,228Ra, and224Ra), the activities rapidly reach a constant or quasi-constant activity value. For226Ra and222Rn, the limiting activity is reached after 1 km. High δ234U values (proportional to the ratioɛ234Th/W238U) can be obtained through high recoil fraction and/or low weathering rates. The activity ratios230Th/232Th,228Ra/226Ra and224Ra/226Ra have been considered in the cases where either weathering or recoil is the predominant process of input from the mineral grain. Typical values for weathering rates and recoil fractions for a sandy aquifer indicate that recoil is the dominant process for Th isotopic ratios in the water. Measured data for Ra isotope activity ratios indicate that recoil is the process generally controlling the Ra isotopic composition in water. Higher isotopic ratios can be explained by different desorption kinetics of Ra. However, the model does not provide an explanation for228Ra/226Ra and224Ra/226Ra activity ratios less than unity. From the model, the highest222Rn emanation equals 2ɛ. This is in agreement with the hypothesis that222Rn activity can be used as a first approximation for input by recoil (Krishnaswamiet al 1982). However, high222Rn emanation cannot be explained by production from the surface layer as formulated in the model. Other possibilities involve models including surface precipitation, where the surface layer is not in steady-state.  相似文献   

3.
《Applied Geochemistry》1999,14(3):365-385
The abundance and chemical/mineralogical form of 226Ra, 238U and 232Th were determined on samples of soil and associated vegetation at 12 sites in the eastern United States. Progressive, selective chemical extraction plus size fractionation determined the abundance and radiometric equilibrium condition of these nuclides in 6 operationally defined soil fractions: exchangeable cations, organic matter, “free” Fe-oxides, sand, silt, and clay.In soils, profile-averaged 226Ra/238U activity ratios (AR) are within 10% of unity for most sites, implying little fractionation of U and Ra when the entire soil profile is considered. However, 226Ra greatly exceeds 238U activity in most surface soil (AR up to 1.8, av 1.22), in vegetation (AR up to 65, av. 2.8), in the exchangeable+organic fraction (AR up to 30, av. 13), in some soil Fe oxides (AR up to 3.5, av. 0.83) and in the C horizons of deeply weathered soils (AR up to 1.5).A major factor in Ra behavior is uptake by vegetation, which concentrates Ra>U and moves Ra from deeper soil to surface soil. Vegetation is capable of creating the observed Ra excess in typical surface soil horizons (AR up to 1.8, av. 1.22) in about 1000 a. Of the total Ra in an average A horizon, 42% occurs as exchangeable ions and in organic matter, but only 6–8% of the parent U and Th occur in these soil forms. In contrast, U is slightly enriched relative to Ra in Fe-oxides of A horizons, implying rapid chemical partition of vegetation-cycled U and Ra.In deeper horizons, transfer by vegetation and/or direct chemical partitioning of Ra into organic and exchangeable forms provides a source for unsupported 226Ra in Ra-rich organic matter, and leaves all soil minerals Ra-poor (AR=0.73). Organic matter evidently has a strong affinity for Ra.The phenomena discussed above are relevant to evaluation of indoor Rn hazard, and behavior of Ra at sites affected by radioactive waste disposal, phosphate tailings, Ra-rich brine, and uraniferous fertilizer.  相似文献   

4.
Abundances of 238U, 234U, 232Th, 226Ra, 228Ra, 224Ra, and 222Rn were measured in groundwaters of the Ojo Alamo aquifer in northwest New Mexico. This is an arid area with annual precipitation of ∼22 cm. The purpose was to investigate the transport of U-Th series nuclides and their daughter products in an old, slow-moving groundwater mass as a means of understanding water-rock interactions and to compare the results with a temperate zone aquifer. It was found that 232Th is approximately at saturation and supports the view of Tricca et al. (2001) that Th is precipitated irreversibly upon weathering, leaving surface coatings of 232Th and 230Th on aquifer grains. Uranium in the aquifer waters has very high [234U/238U] ∼ 9 and low 238U concentrations. These levels can be explained by low weathering rates in the aquifer (w238U ∼ 2 × 10−18 to 2 × 10−17s−1) using a continuous flow, water-rock interaction model. The Ra isotopes are roughly in secular equilibrium despite their very different mean lifetimes. The 222Rn and 228Ra isotopes in the aquifer correspond to ∼10% of the net production rate of the bulk rock. This is interpreted to reflect an earlier formed irreversible surface coating of Th that provides Ra and Rn to the aquifer waters. The surface waters that appear to be feeding the aquifer have low [234U/238U] and high 238U concentrations. The flow model shows that it is not possible to obtain the high [234U/238U] and low [238U] values in the aquifer from a source like the present vadose zone input. It follows that the old aquifer waters studied cannot be fed by the present vadose zone input unless they are greatly diluted with waters with very low U concentrations. If the present sampling of vadose zone sources is representative of the present input, then this requires that there was a major change in water input with much larger rainfall some several thousand years ago. This may represent a climatic change in the Southwest.  相似文献   

5.
In order to unravel magma processes and the geochemical evolution of shallow plumbing systems beneath active volcanoes, we investigated U-series disequilibria of rocks erupted over the past 500 years (1469-2000 AD) from Miyakejima volcano, Izu arc, Japan. Miyakejima volcanic rocks show 238U-230Th-226Ra disequilibria with excess 238U and 226Ra, due to the addition of slab-derived fluids to the mantle wedge. Basaltic bombs of the 2000 AD eruption have the lowest (230Th/232Th) ratio compared to older Miyakejima eruptives, yielding the youngest 238U-230Th model age of 2 kyr. This reinforces our previous model that fluid release from the slab and subsequent magma generation in the mantle wedge beneath Miyakejima occur episodically on a several-kyr timescale. In the last 500 years, Miyakejima eruptives show: (1) a vertical trend in a (230Th/232Th)-(238U/232Th) diagram and (2) a positive linear correlation in a (226Ra/230Th)0 − 1/230Th diagram, which is also observed in lavas from some of the single eruptions (e.g., 1940, 1962, and 1983 AD). The variations cannot be produced by simple fractional crystallization in a magma chamber with radioactive decay of 230Th and 226Ra, but it is possibly produced by synchronous generation of melts in the mantle wedge with different upwelling rate or addition of multiple slab-derived fluids. A much more favorable scenario is that some basaltic magmas were intermittently supplied from deep in the mantle and injected into the crust, subsequently modifying the original magma composition and producing variations in (230Th/232Th) and (226Ra/230Th)0 ratios via assimilation and fractional crystallization (AFC). The assimilant of the AFC process would be a volcanic edifice of previous Miyakejima magmatism. Due to the relatively short timescales involved, the interaction between the assimilant and recent Miyakejima magmatism has not been recorded by the Sr-Nd-Pb isotopic systems. In such cases, Th isotopes and (226Ra/230Th) ratio are excellent geochemical tracers of magmatic evolution.  相似文献   

6.
The increasing interest in radioactivity has brought about the need for an assessment of human exposure to radiation. It is, therefore, necessary to examine naturally occurring radioactivity in the environment, especially its occurrence in groundwater. The aim of this work was then to study the levels and behavior of the most significant natural radionuclides, also in order to improve the knowledge of the hydrochemical processes involved in the selected groundwater systems. Natural radioactivity in fifteen Calabrian groundwaters for human use was investigated through high-resolution gamma spectrometry (with a negative-biased Ortec HPGe detector) and liquid scintillation measurements. Particular attention was given on those radionuclides (3H, 238U, 226Ra, and 228Ra), which contribute in a significant way to the overall effective dose received by members of the public due to the intake of drinking water originating from groundwater systems. The activity concentration of 238U varied from 1 to 51 mBq/L, as a result of the geology of the investigated area and of the oxidizing conditions that favored U dissolution. 226Ra presented a broad range of activity concentrations (0.011–0.14 mBq/L), lower than uranium ones because radium occurs in groundwater under reducing conditions. Some heavy metals (Cd, Pb, Be, Hg, Ag, As, Tl, Sb, Se, and Ni) were also investigated through ICP-MS measurements and compared with the limits set by the Italian Legislation. Metals are released into the environment by both natural and anthropogenic sources; they leach into underground waters, moving along water pathways and eventually depositing in the aquifer.  相似文献   

7.
The activities of the most common, naturally occurring radionuclides 238U, 226Ra, 210Pb, 228Ra, 228Th, and 40K were measured by gamma-ray spectrometry in samples from reservoir rocks, geothermal fluids, and mineral precipitates at the geothermal research site Groß Schönebeck (North German Basin). Results demonstrated that the specific activity of the reservoir rock is within the range of the mean concentration in the upper earth crust of <800 Bq/kg for 40K and <60 Bq/kg for radionuclides of the 238U and 232Th series, respectively. The geothermal fluid showed elevated activity concentrations (up to 100 Bq/l) for 226Ra, 210Pb, and 228Ra, as compared to concentrations found in natural groundwater. Their concentration in filter residues even increased up to 100 Bq/g. These residues contain predominantly two different mineral phases: a Sr-rich barite (Sr, BaSO4) and laurionite (PbOHCl), which both precipitate upon cooling from the geothermal fluid. Thereby they presumably enrich the radionuclides of Ra (by substitution of Ba) and Pb. Analysis of these precipitates further showed an increased 226Ra/228Ra ratio from around 1–1.7 during the initial months of fluid production indicating a change in fluid composition over time which can be explained by different contributions of stimulated reservoir rock areas to the overall produced fluid.  相似文献   

8.
Analyses have been made of many groundwater samples, some of which were collected from the vicinity of uranium deposits and others from unmineralized areas, for dissolved uranium and for the four naturally occurring isotopes of radium: 226Ra (238U decay series, y), 228Ra and 224Ra (232Th decay series, y and 3.8 d) and 223Ra (235U decay series, d). The radium isotopes 226Ra, 224Ra and 223Ra, are measured by alpha-spectrometry after extraction from a water sample soon after collection and 228Ra at a later time by determining the amount of ingrown 212Po.  相似文献   

9.
采用氢氟酸-硝酸-盐酸混合酸密闭消解含铀矿石样品,用阴离子交换树脂、阳离子交换树脂和锶特效树脂逐级分离富集铀、钍和镭。使用高分辨电感耦合等离子体质谱(HR-ICPMS)测定分离纯化液中234U/238U2、30Th/232Th和228Ra/226Ra同位素。比值的测量精密度取决于比值的大小和对应核素浓度的大小。对质量浓度为10 ng/mL天然铀测量液,234U/238U的测量精密度优于1.2%;对230Th质量浓度为0.6ng/mL且230Th和232Th质量浓度接近的测量液,230Th/232Th的测量精密度为1.2%;对228Ra质量浓度为0.48 pg/mL且228Ra和226Ra质量浓度接近的测量液,228Ra/226Ra的测量精密度为4.0%。  相似文献   

10.
The variation of the natural radionuclide concentrations depends on the chemical composition of each site. In this work, two thermal springs in the east of Algeria have been chosen to assess the activity concentration of natural radionuclide, mainly the three natural radioactive series 238U, 235U and 232Th, and 40K. The high-resolution gamma ray spectroscopy was used to determine these concentrations. In these water samples, 235U, 234Th, 210Pb, 226Ra radionuclides are less than the minimum detectable activity. The activity of 238U is dominant. The 238U activity was determined by taking the mean activity of two separate photo-peaks of daughter nuclides 214Pb at 351.92 (37.2%) keV and 214Bi at 609.31 (45%) keV. The measured activity concentrations of 238U in water samples obtained from the concentrations of 214Bi and 214Pb ranged from 0.56 ± 0.20 to 1.13 ± 0.20 Bq/L. The annual effective dose value due to the ingestion of the measured radionuclide 238U in 1 L of water, for an adult, ranged from 9.20 to 18.56 µSv.  相似文献   

11.
青岛市天然放射性环境地质调查   总被引：2，自引：0，他引：2  
对青岛地区进行了大规模的天然放射性环境地质调查和评价中发现,青岛地区陆地伽马辐射剂量率虽然略高于全国和山东省的平均水平,但仍属于天然辐射安全区域.测区的伽马辐射剂量率值总体上决定于岩性.伽马辐射剂量率都来自于238U、232Th、40K的贡献,但是与其他地区不同,40K和232Th对剂量率的贡献要大于238U.此外,一些公路、建筑等建造材料中的放射性核素的含量直接影响着这些工程的放射剂量,主要是在建造这些工程时所选用的石材、石料和水泥等,都会对当地的放射剂量有着重大的影响.  相似文献   

12.
Measurements of 238U-230Th-226Ra disequilibria, Sr-Nd-Pb-Hf isotopes and major-trace elements have been conducted for lavas erupted in the last quarter-millennium at Hekla volcano, Iceland. The volcanic rocks range from basalt to dacite. Most of the lavas (excluding dacitic samples) display limited compositional variations in radiogenic Sr-Nd-Pb-Hf isotopes (87Sr/86Sr = 0.70319-0.70322; 143Nd/144Nd = 0.51302-0.51305; 206Pb/204Pb = 19.04-19.06; 207Pb/204Pb = 15.53-15.54; 208Pb/204Pb = 38.61-38.65; 176Hf/177Hf = 0.28311-0.28312). All the samples possess (230Th/238U) disequilibrium with 230Th excesses, and they show systematic variations in (230Th/232Th) and (238U/232Th) ratios. The highest 226Ra excesses occur in the basalt and most differentiated andesite lavas, while some basaltic-andesite lavas have (226Ra/230Th) ratio that are close to equilibrium. The 238U-230Th-226Ra disequilibria variations cannot be produced by simple closed-system fractional crystallization with radioactive decay of 230Th and 226Ra in a magma chamber. A closed-system fractional crystallization model and assimilation and fractional crystallization (AFC) model indicate that the least differentiated basaltic andesites were derived from basalt by fractional crystallization with a differentiation age of ∼24 ± 11 kyr, whereas the andesites were formed by assimilation of crustal material and fractionation of the basaltic-andesites within 2 kyr. Apatite is inferred to play a key role in fractionating the parent-daughter nuclides in 230Th-238U and 226Ra-230Th to make the observed variations. Our proposed model is that several batches of basaltic-andesite magmas that formed by fractional crystallization of a basaltic melt from a deeper reservoir, were periodically injected into the shallow crust to form individual magma pockets, and subsequently modifying the original magma compositions via simultaneous assimilation and fractional crystallization. The assimilant is the dacitic melt, which formed by partial melting of the crust.  相似文献   

13.
High concentrations of U and226Ra, and elevated234U/238U activity ratios have been measured in groundwater samples collected from water supply wells and exploratory boreholes in the area surrounding the Underground Research Laboratory (URL) of Atomic Energy of Canada Limited, in southeastern Manitoba. All groundwaters come from the Lac du Bonnet granite batholith or sediments overlying the batholith.Uranium concentrations attain almost 1 mg/l in some shallow, low-salinity groundwaters, whereas226Ra tends to be high (up to 38 Bq/l) in deeper, saline waters. The U concentrations are some of the highest observed in global groundwaters, yet no significant ore body or mineralization is known in the area. Analyses of unaltered rock samples of the Lac du Bonnet granite show slight U enrichment over average Canadian Shield granites (6.5 μg/g vs 4 μg/g), and altered wall rock in fracture zones is enriched in U by up to an order of magnitude compared to adjacent bedrock. Low234U/238U activity ratios in this altered rock indicate active and recent leaching of U by groundwater.The key control on U concentration appears to be redox potential. Concentrations of U in rock, residence time and groundwater composition are of lesser importance. Geochemical modelling of the shallower, oxidized waters indicates that U speciation consists mainly of anionic carbonate complexes of the uranyl ion. This is supported by the remarkable efficiency of an anionic filter developed to remove high levels of U from drinking water in the area.In more reducing groundwaters, U concentrations are similar to those determined in recent experimental work on uraninite solubility in the pH range 7–8.5. Colloidal U is <10% of total U and organic complexation is unlikely to be significant because of low dissolved organic concentrations. The results emphasize the significance of redox potential in controlling U mobility in both oxidizing and reducing environments and indicate the usefulness of U concentration in estimating groundwater Eh.  相似文献   

14.
The Aral Sea has been shrinking since 1963 due to extensive irrigation and the corresponding decline in the river water inflow. Understanding of the current hydrological situation demands an improved understanding of the surface water/groundwater dynamics in the region. 222Rn and 226Ra measurements can be used to trace groundwater discharge into surface waters. Data of these radiometric parameters were not previously available for the study region. We determined 222Rn activities after liquid phase extraction using Liquid Scintillation Counting (LSC) with peak-length discrimination and analyzed 226Ra concentrations in different water compartments of the Amu Darya Delta (surface waters, unconfined groundwater, artesian water, and water profiles from the closed Large Aral Sea (western basin).The water samples comprise a salinity range between 1 and 263 g/l. The seasonal dynamics of solid/water interaction under an arid climate regime force the hydrochemical evolution of the unconfined groundwater in the Amu Darya Delta to high-salinity Na(Mg)Cl(SO4) water types. The dissolved radium concentrations in the waters were mostly very low due to mineral over-saturation, extensive co-precipitation of radium and adsorption of radium on coexisting solid substrates.The analysis of very low 226Ra concentrations (<10 ppq) at remote study sites is a challenge. We used the water samples to test and improve different analytical methods. In particular, we modified a procedure developed for the α-spectrometric determination of 226Ra after solid phase extraction of radium using 3M Empore™ High Performance Extraction Disks (Purkl, 2002) for the analysis of the radionuclide using an ICP sector field mass spectrometer. The 226Ra concentration of 17 unconfined groundwater samples ranged between 0.2 and 5 ppq, and that of 28 artesian waters between <0.2 and 13 ppq. The ICP-MS results conformed satisfactorily to analytical results based on γ-measurements of the 222Rn ingrowth after purging and trapping on super-cooled charcoal. The 226Ra concentrations were positively correlated with the salinity and the dissolved NaCl concentrations. The occurrence of unusually high 226Ra activities is explained by radium release from adsorption sites with increasing salinity. The inferred spatial variability of 222Rn in the Aral Sea and of 222Rn and 226Ra in the groundwater of the Amu Darya Delta is discussed in the context of our own previous hydrochemical studies in the study sites. Relatively low 222Rn activities in the unconfined GW (1–9.5 Bq/l) indicate the alluvial sediments hosting the GW to be a low-238U(226Ra) substrate. Positive correlations between U and 226Ra, and U and 222Rn are likely related to locally deposited Fe(Mn)OOH precipitates. The 222Rn activity of the GW, however, distinctly exceeds the 222Rn concentration in the Aral Sea (10 mBq/l), in principle, making 222Rn a sensitive tracer for the inflow of GW. The high water volume of the Large Aral Sea and wind induced mixing of its water body, however, hamper the detection of local groundwater inflow.  相似文献   

15.
Relatively high activity concentrations of some radionuclides (226Ra, 238U, 232Th, and 40K) have been measured in surface and subsurface soils in areas (southern Iraq) where many warfare actions have taken place during the Iran–Iraq and Gulf wars. Such high activity concentrations might be related to the increase in cancerous injuries and birth defects recently reported. The study was aimed to estimate the activity concentrations of some nuclides and a comparison of results with international health hazard indices. In addition, the excess lifetime cancer risk (ELCR) was assessed. Soil samples were collected at three depths (0, 30, and 60 cm) in three locations in Abu Al Khasib and Ad Dayr in Basrah governorates. The average activity concentrations were estimated employing hyper-pure germanium HPGe gamma-ray detection technology. The values obtained in Abu Al Khasib were: 58.44 Bq/kg (226Ra), 43.56 Bq/kg (238U), 19.38 Bq/kg (232Th), and 321.76 Bq/kg (40K) whereas in Ad Dayr 45.71 Bq/kg (226Ra), 35.53 Bq/kg (238U), 20.33 Bq/kg (232Th), and 337.02 Bq/kg (40K). According to UNSCEAR (Sources and effects of ionizing radiations: a report on the effects of atomic radiation to the general assembly with scientific annexes, Annex B, United Nations, New York, 2000) report, higher levels of 226Ra, 238U concentrations than the world’s average values (35 Bq/kg) were observed in both locations. In addition, some radiation hazard indices were determined for both locations: average outdoor external dose (D out), average indoor external dose (D in), total average value of the external dose (D tot), average annual outdoor effective dose (E out), average annual indoor effective dose (E in), and averaged total annual effective dose (E tot). Values for D tot and E tot were higher than the worldwide median (143 nGy/h and 0.48 mSv/y, respectively) in both regions. The measured values of activity concentrations were also used to estimate the outdoor, indoor, and total ELCR. The ELCR values were higher than the worldwide averages. Further analyses and studies need to assess the real risks for human health and possible soil remediation.  相似文献   

16.
《Applied Geochemistry》2002,17(6):781-792
Samples of tuff from boreholes drilled into fault zones in the Exploratory Studies Facility (ESF) and relatively unfractured rock of the Cross Drift tunnels, at Yucca Mountain, Nevada, have been analysed by U-series methods. This work is part of a project to verify the finding of fast flow-paths through the tuff to ESF level, indicated by the presence of ‘bomb’ 36Cl in pore fluids. Secular radioactive equilibrium in the U decay series, (i.e. when the radioactivity ratios 234U/238U, 230Th /234U and 226Ra/230Th all equal 1.00) might be expected if the tuff samples have not experienced radionuclide loss due to rock-water interaction occurring within the last million years. However, most fractured and unfractured samples were found to have a small deficiency of 234U (weighted mean 234U/238U=0.95±0.01) and a small excess of 230Th (weighted mean 230Th/234U 1.10±0.02). The 226Ra/230Th ratios are close to secular equilibrium (weighted mean=0.94±0.07). These data indicate that 234U has been removed from the rock samples in the last ∼350 ka, probably by pore fluids. Within the precision of the measurement, it would appear that 226Ra has not been mobilized and removed from the tuff, although there may be some localised 226Ra redistribution as suggested by a few ratio values that are significantly different from 1.0. Because both fractured and unfractured tuffs show approximately the same deficiency of 234U, this indicates that pore fluids are moving equally through fractured and unfractured rock. More importantly, fractured rock appears not to be a dominant pathway for groundwater flow (otherwise the ratio would be more strongly affected and the Th and Ra isotopic ratios would likely also show disequilibrium). Application of a simple mass-balance model suggests that surface infiltration rate is over an order of magnitude greater than the rate indicated by other infiltration models and that residence time of pore fluids at ESF level is about 400 a. Processes of U sorption, precipitation and re-solution are believed to be occurring and would account for these anomalous results but have not been included in the model. Despite the difficulties, the U-series data suggest that fractured rock, specifically the Sundance and Drill Hole Wash faults, are not preferred flow paths for groundwater flowing through the Topopah Spring tuff and, by implication, rapid-flow, within 50 a, from the surface to the level of the ESF is improbable.  相似文献   

17.
研究了TIMS测定铀矿石样品中234U/238U、230Th/232Th、228Ra/226Ra的方法。建立了铀矿石密闭混酸一次溶样的方法和采用阴离子、阳离子和Sr特效树脂逐级离子交换分离纯化U、Th和Ra的流程,满足了TIMS测量要求。测定结果表明：100～1000 ng的天然铀中234U/238U,其测量精密度从静态多接收的2.34%提高到动态多接收的0.47%;对230Th与232Th丰度接近、质量为1μg左右的钍,采用三带点样技术和法拉第多接收技术测定230Th/232Th,其内精度平均值为0.0048%,外精度为0.028%;采用单带加钽发射剂,ETP跳峰测定50～100 fg镭-228稀释剂中的228Ra/226Ra,其内精度小于0.10%,外精度小于0.20%。比较TIMS和HR-ICP-MS、α能谱法测定234U/238U、230Th/232Th、228Ra/226Ra结果,三者结果相吻合。TIMS测量法样品用量少、快速、准确、精密度高,是U、Th、Ra同位素比值测定方法的又一补充。  相似文献   

18.
The geochemistry of Ba, Ra, Th, and U and the potential of using 226Ra/Ba ratios as an alternative dating method are explored in modern and Holocene marine mollusc shells. Five modern shells of the Antarctic scallop Adamussium colbecki collected from the present day beach and six radiocarbon dated specimens from Holocene beach terraces of the Ross Sea region (Antarctic) between 700 and 6100 calibrated yr BP old have been analysed by mass spectrometry. In clean shells 226Ra concentrations and 226Ra/Ba ratios show a clear decrease with increasing age, suggesting the possibility of 226Ra dating. Limiting factors for such dating are Ba and 226Ra present in surface contaminants, and ingrowth of 226Ra from U present within the shell. Surface contamination is difficult to clean off entirely, but moderate levels of residual contamination can be corrected using 232Th. Sub-samples from the same shell with different proportions of contamination form a mixing line in a 226Ra/Ba-232Th/Ba graph, and the 226Ra/Ba of the pure shell can be derived from the intercept on the 226Ra/Ba axis. Contaminant corrected 226Ra/Ba ratios of late-Holocene 14C-dated samples fall close to that expected from simple 226Ra excess decay from seawater 226Ra/Ba values. 226Ra ingrowth from U incorporated into the shell during the lifetime of the mollusc can be corrected for. However, the unknown timing of post mortem U uptake into the shell makes a correction for 226Ra ingrowth from secondary U difficult to achieve. In the A. colbecki shells, 226Ra ingrowth from such secondary U becomes significant only when ages exceed ∼2500 yr. In younger shells, 226Ra/Ba ratios corrected for surface contamination provide chronological information. If evidence for a constant oceanic relationship between 226Ra and Ba in the ocean can be confirmed for that time scale, the 226Ra/Ba chronometer may enable the reconstruction of variability in sea surface 14C reservoir ages from mollusc shells and allow its use as a paleoceanographic tracer.  相似文献   

19.
为了掌握陕西省石煤矿的辐射环境现状,对陕西省3个石煤矿进行了放射性水平调查,结果表明陕西省石煤中238 U、226 Ra平均比活度分别为当地环境本底的26~35倍、19~30倍,γ辐射水平为当地天然环境本底的4~7倍,各工作场所及周边环境的222 Rn及其子体浓度处于正常范围之内。石煤开发活动所致矿区作业人员、公众年附加有效剂量满足国家标准相关限值要求。  相似文献   

20.
Levels of naturally occurring radioactivity in sediment samples of Beni Haroun dam have been investigated. The activity concentrations of 238U and 232Th decay chains and 40K primordial radionuclide have been measured using high-resolution HPGe detector. Activity concentrations of 226Ra, 232Th, and 40K radionuclides were found in the ranges 9–66, 14–37, and 177–288 Bq/kg with the mean values 24.67, 25.98, and 208.10 Bq/kg, respectively. Radiological hazard parameters were estimated based on the activity concentrations for 226Ra, 232Th, and 40K to find out any radiation hazard associated with the sediments. Correlation studies between pairs of radionuclides were performed and discussed, and the obtained results are compared with international recommended values.  相似文献   

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