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1.
《Applied Geochemistry》1993,8(6):605-616
The Cigar Lake U deposit is located in northern Saskatchewan in the eastern part of the Athabasca Sandstone Basin, and consists of a high-grade ore body (up to 55% U) located at a depth of ∼430 m. As part of a study to evaluate the analog features of this deposit with respect to a disposal vault for waste nuclear fuel, colloids (1–450 nm) and suspended particles (450nm) in groundwater have been investigated to evaluate their effect on element transport through the U deposit. Tangential-flow ultrafiltration was used to concentrate particles from 501 groundwater samples in order to characterize the size distribution, concentration, composition and natural radionuclide content of particles in representative parts of the U deposit. Although Cigar Lake groundwaters contain particles in all sizes ranging from 10 nm to slightly larger than 20 μm, most samples contained a relatively high concentration of colloids in the 100–400 nm size range. Particle compositions are similar to the composition of minerals in the sandstones and ore body, suggesting that particles in groundwater are generated by the erosion of fracture-lining minerals. As a result, particle concentrations in groundwater are affected by the integrity of the host rock. In some piezometers the high initial concentrations of suspended particles, which may have been drilling artifacts, decreased during the collection of the first 350 1. Although colloid concentrations fluctuated during sampling, there are no indications that these concentrations will be permanently reduced by continued groundwater pumping. The observed colloid and suspended particle concentrations in the deep groundwaters are too low to have a significant impact on radionuclide migration, provided that radionuclide sorption is reversible. If radionuclides are irreversibly sorbed to particles they cannot sorb to the host rock and their migration can only be evaluated with an understanding of particle mobility. The data for dissolved and particulate U, Th and Ra were used to calculate field-derived distribution ratios (Rd) between particles and groundwater. The wide range of observed Rd values indicates that these radionuclides in particulate form are not in equilibrium with groundwater. U-series isotope data indicated that most of the U and Ra on particles was derived from groundwater. Some particles could have retained their U for as long as 8000 a. The U and Ra contents of particles in the ore and surrounding clay zones are significantly higher than in particles from sandstone, suggesting that the clay has been an effective barrier to particle migration.  相似文献   

2.
《Applied Geochemistry》1996,11(3):387-402
Naturally occurring organics in groundwaters of the Whiteshell Research Area (WRA) of southern Manitoba were investigated to assess their potential role in radionuclide transport within granite fractures of the Canadian Shield. A survey of dissolved organic carbon concentrations, carried out to determine the variability in the organic content of these groundwaters, showed average concentrations of 0.8 ± 0.1 mg/L for Fracture Zone 2, 0.8 ± 0.4 mg/L for near-vertical fractures and 2.3 ± 0.8 mg/L for deeper saline groundwater. The dissolved organic carbon consisted mainly of hydrophilic neutral compounds (60 to 75%), and hydrophobic and hydrophilic acids (23 to 39%), along with very small amounts of hydrophobic bases and neutrals, and hydrophilic bases. Significant contamination from drilling operations and plastics, mostly in the form of hydrophobic neutrals, was observed in some samples. These compounds would not contribute to radionuclide migration in a natural system and are not included in the assessment of the organic complexing capacity of these groundwaters.Based on groundwater concentrations of hydrophobic and hydrophilic acids and on the measured car☐ylic functional group content of these acids, the average complexing capacity of natural organics in Whiteshell Research Area groundwaters was calculated to be 2.9 × 10−6 eq/L. The ability of these organics to complex radionuclides was tested using conditional stability constants from the literature for humic complex formation with Am(III), Th(IV), and U(VI). The chemistry of U(VI) was predicted to be dominated by inorganic complexes and not significantly affected by organics. The literature contains a wide range in values of stability constants for Am(III) and Th(IV) complexes with humics. The aqueous chemistry of Am(III) and Th(VI) could be affected by complexation with natural organics if the higher stability constant values are valid for WRA groundwaters.  相似文献   

3.
Data are presented on suspended particles and colloids in groundwaters from the Osamu Utsumi mine and the Morro do Ferro analogue study sites. Cross-flow ultrafiltration with membranes of different pore sizes (450 nm to 1.5 nm) was used to prepare colloid concentrates and ultrafiltrates for analyses of major and trace elements and U- and Th-isotopic compositions. Additional characterization of colloidal and particulate material was performed by ESCA, SEM and X-ray diffraction. The results indicate the presence of low concentrations of colloids in these waters (typically < 500 μg/l), composed mainly of iron/organic species. Minor portions of uranium and other trace elements, but significant fractions of the total concentrations of Th and REE in prefiltered waters (< 450 nm) were associated with these colloids.Suspended particles (> 450 nm), also composed mainly of hydrous ferric oxides and humic-like compounds, show the same trend as the colloids with respect to U, Th and REE associations, but elemental concentrations were typically higher by a factor of 1,000 or more. In waters of low pH and with high sulphate content, these associations are considerably lower. Due to the low concentrations of suspended particles in groundwaters from the Osamu Utsumi uranium mine (typically <0.5 mg/l), these particles carry only a minor fraction of U and the REE (<10% of the total concentrations in unfiltered groundwaters), but a significant, usually predominant fraction of Th (30–70%). The suspended particle load in groundwaters from the Morro do Ferro environment is typically higher than in those from the mine by a factor of 5 to 10. This suggests that U, Th and the REE could be transported predominantly by particulate matter. However, these particles and colloids seem to have a low capacity for migration.  相似文献   

4.
Natural colloids have a potential role in facilitating the transport of radionuclides in groundwater. To assess the role of mobile colloidal phases in radionuclide transport, characterization of colloids for size, size distribution, zeta potential, surface charge and elemental composition is required. Groundwater samples were collected from 12 borewells in the study area and were characterized with respect to physicochemical parameters. Water quality parameters such as pH, temperature, specific conductance, TDS and dissolved O2 were measured in situ. Based on salinity, two groundwater types were identified in the study area: (1) freshwater type and (2) brackish type. Laboratory and field-scale turbidity measurements in addition to quantitative analysis of major ions were carried out. It was observed that the colloid concentrations are reduced at higher salinity. Zetasizer, particle size analyzer, scanning electron microscopy, energy dispersive X-ray analysis and X-ray diffraction techniques were used to characterize the colloidal particles in groundwater. Colloids were present in all the groundwater samples, the concentration varying between 0.05 and 6 mg/L. Colloid concentration was greater in wells with low ionic strength and the number of colloidal particles varied between 3 × 109 and 4 × 1011 particles/L. The average colloid size varied between 200 and 350 nm for various samples. The zeta potential of the colloidal particles varied between −25.5 and –34.0 mV. SEM analysis of colloidal particles revealed the presence of clays particularly kaolinite and that the mineral composition of colloids reflects the mineralogy of the aquifer. For proper risk assessment and remediation studies, the role of colloids in radionuclide transport assumes greater importance. This study highlights the need for, and relevance of, detailed colloid characterization to assess its role in the migration of radionuclides from near surface disposal facilities.  相似文献   

5.
To evaluate the risk of contaminant transport by mobile colloids, it is necessary to understand how colloids and associated pollutants behave during their migration through uncontaminated soil or groundwater. In this study, we investigated the influence of aggregation induced by Ca2+ and trace metals (Pb2+, Cu2+) concentrations on the transport of humic-coated kaolinite colloids through a natural quartz sand at pH=4. Adsorbed divalent cations reduce the colloids surface charge and thereby induce aggregation and deposition in porous media. To cite this article: R. Ait Akbour et al., C. R. Geoscience 334 (2002) 981–985.  相似文献   

6.
《Applied Geochemistry》1998,13(1):31-42
Organic material typically constitutes a substantial volume (∼ 90%) of the low-level radioactive wastes (LLRW) intended for near-surface disposal at Chalk River Laboratories (CRL), Ontario, Canada. These wastes can contain a large variety of organic materials, including paper, cardboard, plastic bags, used clothing, and mop heads. After emplacement in a disposal facility, leaching of the LLRW by water can mobilize inorganic and organic substances, ranging from small molecules such as acetic acid to unidentifiable material of colloidal size range. This study determined the potential for colloid formation produced by LLRW degradation, because colloid-facilitated transport of contaminants could affect the safety performance of a disposal facility.The decomposition of compacted LLRW was simulated by recirculating water in a closed system over several compacted bales of waste to determine the potential composition and colloid content of leachates. Size fractionation of organic matter was performed on leachate samples that had been aged for 18 months to simulate the microbial degradation of organic matter within leachates during migration out of the LLRW disposal facility. The aged leachates contained high concentrations of dissolved organic matter, ranging between 74 and 5074 mg/l as C. In most of the leachates, volatile fatty acids accounted for a significant fraction (up to 81%) of the dissolved organic carbon. Although 5–110 mg/l of organic colloids were observed in leachates, in most cases, the organic colloids made up a very small fraction of the total leached organic carbon. Therefore, since the complexation properties of dissolved and colloidal organics are probably similar, contaminants complexed to organics are most likely to be dissolved and not affected by colloid transport. The leachates also contained significant quantities of Fe and Al, which could potentially precipitate Fe and Al as colloids after oxidation. Although a significant portion of the dissolved Fe may have been produced by the corrosion of the ☐es used to contain the bales, the high Fe concentrations could be representative of leachates from LLRW that contain metallic Fe components. If Fe and Al colloids are stable, stable concentrations in LLRW leachates could be high enough to affect contaminant transport. Therefore, the Fe and Al content of LLRW should be minimized. The concentrations of natural colloids in sandy aquifers, such as those found at CRL are too low to affect contaminant migration significantly.  相似文献   

7.
The interaction of Cs(I), Eu(III), Th(IV) and U(VI) with montmorillonite colloids was investigated in natural Grimsel Test Site groundwater over a 3 years period. The asymmetric flow field-flow fractionation combined with various detectors was applied to study size variations of colloids and to monitor colloid association of trace metals. The colloids suspended directly in the low ionic strength (I), slightly alkaline granitic groundwater (I = 10−3 mol/L, pH 9.6) showed a gradual agglomeration with a size distribution shift from initially 10-200 nm to 50-400 nm within over 3 years. The Ca2+ concentration of 2.1 × 10−4 mol/L in the ground water is believed to be responsible for the slow agglomeration due to Ca2+ ion exchange against Li+ and Na+ at the permanently charged basal clay planes. Furthermore, the Ca2+ concentration lies close to the critical coagulation concentration (CCC) of 10−3 mol L−1 for clay colloids. Slow destabilization may delimit clay colloid migration in this specific groundwater over long time scales. Eu(III) and Th(IV) are found predominantly bound to clay colloids, while U(VI) prevails as the UO2(OH)3 complex and Cs(I) remains mainly as aquo ion under our experimental conditions. Speciation calculations qualitatively represent the experimental data. A focus was set on the reversibility of metal ion-colloid binding. Addition of humic acid as a competing ligand induces rapid metal ion dissociation from clay colloids in the case of Eu(III) even after previous aging for about 3 years. Interestingly only partial dissociation occurs in the case of Th(IV). Experiments and calculations prove that the humate complexes dominate the speciation of all metal ions under given conditions. The partial irreversibility of clay bound Th(IV) is presently not understood but might play an important role for the colloid-mediated transport of polyvalent actinides over wide distances in natural groundwater.  相似文献   

8.
The formation of colloids during the weathering of phyllite was investigated by exposing ground phyllite to Milli-Q water. Secondary mineral colloids of 101–102 nm were detected in significant concentrations. At pH of about 8.5, the solution concentration of these colloids reached up to 10 mg/L (however, acidification to pH 4.0 prevented the formation of the colloids). The mineralogical composition of the secondary mineral colloids is assumed to be a mixture of ferrihydrite, manganese oxyhydroxides, aluminosilicates, amorphous Al(OH)3 and gibbsite with possible additions of iron silicates and␣iron-alumino silicates. The colloids were stable over longer periods of time (at least several weeks), even in the presence of suspended ground rock. Direct formation of iron-containing secondary mineral colloids at the rock–water interface by the weathering of rock material is an alternative to the well-known mechanism of iron colloid formation in the bulk of water bodies by mixing of different waters or by aeration of anoxic waters. This direct mechanism is of relevance for colloid production during the weathering of freshly crushed rock in the unsaturated zone as for instance crushed rock in mine waste rock piles. Colloids produced by this mechanism, too, can influence the transport of contaminants such as actinides because these colloids have a large specific surface area and a high sorption affinity.  相似文献   

9.
The interaction of aluminophosphate glass with water at 95°C for 35 days results in glass heterogenization and in the appearance of a gel layer and various phases. The leaching rate of elements is low owing to the formation of a protective layer on the glass surface. It is shown that over 80% of uranium leached from the glass matrix occurs as colloids below 450 nm in size characterized by high migration ability in the geological environment. To determine the composition of these colloids is a primary task for further studies. Water vapor is a crystallization factor for glasses. The conditions as such may appear even at early stages of glass storage because of the failure of seals on containers of high-level radioactive wastes. The examination of water resistance of crystallized matrices and determination of the fraction of radionuclide in colloids are also subjects for further studies.  相似文献   

10.
《Applied Geochemistry》2001,16(14):1653-1662
Strontium-90 (90Sr) is one of the major radioactive contaminants found in DP Canyon at Los Alamos, New Mexico, USA. Radioactive surveys found that 90Sr is present in surface water and shallow alluvial groundwater environments in Los Alamos National laboratory (LANL). Colloids may influence the transport of this radionuclide in surface and groundwater environments in LANL. In this study, the authors investigated the sorption/desorption behavior of radioactive Sr on Ca-montmorillonite and silica colloids, and the effect of ionic strength of water on the sorption of Sr. Laboratory batch sorption experiments were conducted using 85Sr as a surrogate for 90Sr. Groundwater, collected from Well LAUZ-1 at DP Canyon and from Well J-13 at Yucca Mountain, Nevada, and deionized water, were used. The results show that 92–100% of the 85Sr was rapidly adsorbed onto Ca-montmorillonite colloids in all three waters. Adsorption of 85Sr onto silica colloids varied among the three waters. The ionic strength and Ca2+ concentration in groundwater significantly influence the adsorption of 85Sr onto silica colloids. Desorption of 85Sr from Ca-montmorillonite colloids is slower than from silica colloids. Desorption of 85Sr from silica colloids was faster in LAUZ-1 groundwater than in J-13 groundwater and deionized water. The results suggest that clay and silica colloids may facilitate the transport of Sr along potential flowpaths from DP Canyon to Los Alamos Canyon.  相似文献   

11.
《Applied Geochemistry》1988,3(5):535-548
Large-volume groundwater samples were collected at the Nevada Test Site from within a nuclear detonation cavity and from approximately 300 m outside the cavity. The samples were filtered and ultrafiltered, and the filtrates and various particle size fractions were analyzed for chemical composition and radionuclide activity. In samples from both locations, approximately 100% of the transition element (Mn, Co) and lanthanide (Ce, Eu) radionuclides were associated with colloids. Their presence outside the cavity indicates transport in the colloidal form. Distribution coefficients calculated for Ru, Sb, and Cs nuclides from both field sample locations indicate equilibrium partitioning on the 0.05-0.003 μm colloids. Calculation of transport efficiencies relative to colloid mass concentrations and dissolved neutral or anionic nuclides indicates that both the cations and the radiolabelled colloids appear to experience capture by or exchange with immobile aquifer surfaces.  相似文献   

12.
 Hindustan Polymers Limited was established in the Venkatapuram area in the northwestern part of Visakhapatnam urban agglomeration. Untreated industrial effluent from the plant is discharged with total dissolved solids concentrations reaching up to 6500 mg/l. The groundwater pollution was identified as early as 1981 and a hydrogeologic and water-quality database is available from 1981. The groundwater quality in the plant environs is found to be in the range of 3500–4500 mg/l. Major chemical constituents of industrial-waste waters consist of Na, Cl, and SO4. Some characteristic parameters of the aquifer were estimated. The available hydrogeologic and hydrologic data was analyzed to conceptualize the groundwater regime. A mathematical groundwater flow model was constructed to compute the hydraulic head at the center of finite-difference grid. The computed head distribution and effective porosity of the formations were used to calculate the groundwater flow velocity. The computed velocity field was ultimately used to prognose the pollutant migration in groundwater accounting for the advection and dispersion processes in the mass transport model and for determining the time-dependent pathlines of pollutant. Areal migration of pollutants from the source was predicted up to year 2002. Received: 23 December 1996 · Accepted: 9 September 1997  相似文献   

13.
Tanneries located in an industrial development area of Ranipet (India) manufactured chromate chemicals during 1976?C1996. A large quantity of associated hazardous solid wastes has been stacked about 5-m high above ground level, spread over 3.5?ha inside one of the factory premises. The study area receives an average annual rainfall of 1,100?mm. The granitic formation in the northern part of Palar River catchment has high infiltration rates and has resulted in fast migration of the contamination to the water table. Chromium levels in the groundwater were found up to 275?mg/l. The available hydrogeological, geophysical and groundwater quality data bases have been used to construct a groundwater flow and mass transport model for assessing the groundwater contamination and it has been calibrated for the next 30?years. The migration has been found to be very slow, with a groundwater velocity of 10?m/year. This is the first field-scale study of its kind in this industrial area. The findings are of relevance to addressing the groundwater pollution due to indiscriminate disposal practices of hazardous waste in areas located on the phreatic aquifer. Further, it has been reported that the untreated effluent discharge adjacent to the chromium dump site is most influential in the migration of contaminants.  相似文献   

14.
Data are presented on rare-earth elements (REE) in prefiltered (<450 nm) near-surface and deeper groundwaters and in corresponding particulate matter (>450 nm) from the Osamu Utsumi uranium mine and the Morro do Ferro thorium-REE-deposit. Groundwaters from both sites typically contain between 1–50 μg/l of total REE, but can reach values of up to 160 μg/l in the deepest borehole F4 (U-Mine: 150–415 m). Even higher REE concentrations of up to 29 mg/l were measured in acidic, sulfate-rich near-surface waters of the same site. The chondrite-normalized REE patterns in deeper, more reducing groundwaters and in their corresponding suspended particle fractions are similar to those observed in the bedrock (phonolites), indicating that bedrock leaching and secondary mineral sorption occurred without significant fractionation between these elements, in accordance with the only small variations in the stability constants of the expected REE-sulfate complexes in these waters. Groundwaters from the unsaturated zone of both sites show a very characteristic cerium depletion (less pronounced than that observed in the corresponding suspended particulate fractions), which is most probably related to the oxidation of Ce (III) under the prevailing Eh-conditions of these waters (600 to 800 mV), and to sorption/precipitation reactions of the much less soluble Ce(IV) species. Coarse particulate matter (>450 nm), composed mainly of amorphous ferric hydrous oxides, has a strong capacity for sorption of REE. This is shown by its very high REE concentrations, in some boreholes > 8,000 μg/g (total REE), and by the calculated association ratios Ra (ml/g), which are in the order of 105 to 106. The implications of these findings for the migration behavior of REE in both environments are discussed.  相似文献   

15.
Compacted bentonite has been considered as a candidate buffer material in the underground repository for the disposal of high-level radioactive waste. An erosion of bentonite particles caused by a groundwater flow at the interface of a compacted bentonite and a fractured granite was studied experimentally under various geochemical conditions. The experimental results showed that bentonite particles could be eroded from a compacted bentonite buffer by a flowing groundwater depending upon the contact time, the flow rate of the groundwater, and the geochemical parameters of the groundwater such as the pH and ionic strength.

A gel formation of the bentonite was observed to be a dominant process in the erosion of bentonite particles although an intrusion of bentonite into a rock fracture also contributed to the erosion. The concentration of the eroded bentonite particles eroded by a flowing groundwater was increased with an increasing flow rate of the groundwater. It was observed from the experiments that the erosion of the bentonite particles was considerably affected by the ionic strength of a groundwater although the effect of the pH was not great within the studied pH range from 7 to 10. An erosion of the bentonite particles in a natural groundwater was also observed to be considerable and the eroded bentonite particles are expected to be stable at the given groundwater condition.

The erosion of the bentonite particles by a flowing groundwater did not significantly reduce the physical stability and thus the performance of a compacted bentonite buffer. However, it is expected that an erosion of the bentonite particles due to a groundwater flow will generate bentonite particles in a given groundwater condition, which can serve as a source of the colloids facilitating radionuclide migration through rock fractures.  相似文献   


16.
Mathura oil refinery was commissioned during 1977 and effluent storage ponds were constructed at the same time. These storage ponds receive wastewater from the refinery at a rate of 10000 m3/day. After treatment, waste water is discharged through a 3-km pipeline to a stream leading to the Yamuna river. The groundwater-monitoring as well as water-quality monitoring was carried at 24 observation wells in the refinery site during 1997. The water quality measurements indicated total dissolved chloride and sulphate concentration of native groundwater as 400 mg/l, whereas elevated levels up to 600 mg/l were found at the wells close to polishing ponds. Thus combined transport of chloride and sulphate was simulated in the mass transport model. A three-dimensional flow, pathlines and mass transport model of the aquifer system were constructed to analyze the impact of seepage from polishing ponds contaminating the groundwater regime. The permeability of aquifer varies between 1.5–2.5 m/day. The porosity of formation was assumed as 0.2. The constant head and constant concentration boundaries were assigned to the nodes representing effluent storage ponds. Longitudinal dispersivity of 100 m, horizontal transverse dispersivity of 10 m and vertical transverse dispersivity of 0.01 m were assumed. The mass transport model was calibrated for 20 years by comparing total dissolved chloride and sulphate concentrations from 1997. The model predictions indicate further migration of contaminants on the east of effluent ponds in future. Received: 4 January 1999 · Accepted: 12 July 1999  相似文献   

17.
In this paper, a simple scenario and probabilistic approach is used to assess the potential groundwater risk due to proposed overdraft remedial actions in cone of depression, Jining City, China. Focusing on the concentrations of Chloride ions (Cl) and total hardness (TH), the impact of artificial recharge and reduced pumping on groundwater quality and quantity is analysed by using the three-dimensional finite difference groundwater flow and transport model, Visual MODFLOW, to simulate groundwater flow and transport within the study area based on scenarios, and utilizes SURFER software to map risk levels. Although 5, 10 or 15% reduced pumping with artificial recharge leads to more decrease in Cl and TH concentrations than the 25%, less volume increase is achieved for the remediation of land subsidence and other environmental problems in the cone of depression. The Cl concentrations in recovered groundwater are within the desired concentration of 200 mg/l; however, TH in some cases are above the maximum permissible limit of 500 mg/l, with an exceedence probability of about 0.67 for recharge and recharge with reduced pumping at 25%. The presence of fractures and hydrogeological complexity greatly determines impacts of remediation, and the 22% reduced pumping with artificial recharge offers an optimum strategy for overdraft remediation in the Jining cone of depression.  相似文献   

18.
为了对地下水系统中天然胶体与Ni2+的共迁移特征进行研究,通过静态吸附实验和石英砂模拟含水层介质柱实验研究了土壤胶体对Ni2+在地下水中运移的影响,以及pH、离子强度(IS)、有机质等对土壤胶体吸附Ni2+的影响。结果表明:随着pH值升高,土壤胶体对Ni2+的吸附量增加;离子强度的增加会显著地降低土壤胶体吸附Ni2+的能力;腐殖酸(HA)的存在会增强胶体对Ni2+的吸附能力;在有胶体的情况下,Ni2+穿透砂柱的时间会缩短,吸附能力增强,吸附量增加,但当离子强度增加时,虽然Ni2+穿透砂柱的时间也被缩短,但是吸附量却降低。  相似文献   

19.
In Russia, until recently, it was considered that groundwater was protected from surface radioactive contamination by soil and rocks in the zone aeration. Groundwater was not a subject of radiation control. The accident at the Chernobyl Nuclear Power Plant showed, however, that groundwater is vulnerable to radioactive contamination. In this connection, the vulnerability of groundwater to and the problems of protecting groundwater from radioactive contamination became urgent. The assessment of natural protection of groundwater from radioactive contamination is now considered a top priority. The zone of aeration is generally considered to be the zone separating groundwater from surface contamination. In respect to radioactive contamination, soils that may fix a large quantity of radionuclides serve as a protection zone of a higher order. The mapping of protectibility was done for each radionuclide taking into consideration the specific structure of the flow medium and migration properties of a radionuclide.90Sr and137Cs have different mechanisms of transport; convective transport is characteristic of the former and diffusive transfer of the latter. This is conditioned by different physico-chemical properties of the radionuclides and principally by their sorption capacities. The coefficient of distribution of90Sr is in many times less than the coefficient of distribution of137Cs. The environmental protection problem in regions with nuclear power plants and in areas subjected to radioactive contamination may be solved using a monitoring, system including interrelated systems of observation and prediction of the lithosphere and the hydrosphere. The problem of mathematical modeling of migration processes is related to the complexities of modeling the processes of flow, mass transfer, and the accompanying physicochemical processes in zones of full and partial saturation, as well as difficulties in mathematical calculations.  相似文献   

20.
A groundwater arsenic (As) survey in Mirzapur, Varanasi, Ghazipur, Ballia, Buxar, Ara, Patna, and Vaishali districts of UP and Bihar shows that people from these districts are drinking As-contaminated groundwater (max. 1,300 μg/l). About 66 % of tubewells from Buxar to Mirzapur areas and 89 % of tubewells from Patna to Ballia areas have As?>?10 μg/l (WHO guideline). Moreover, 36 % of tubewells from Buxar to Mirzapur areas and 50 % of tubewells from Patna to Ballia areas have As above 50 μg/l. Most of the As-affected villages are located close to abandoned or present meander channels of the Ganga River. In contrast, tubewells located in Mirzapur, Chunar, Varanasi, Saidpur, Ghazipur, Muhammadabad, Ballia, Buxar, Ara, Chhapra, Patna, and Hazipur towns are As-safe in groundwater because of their positions on the Pleistocene Older Alluvium upland surfaces. The iron (Fe) content in tubewell water samples varies from 0.1 to 12.93 mg/l. About 77 % As-contaminated tubewells are located within the depth of 21 to 40 m in the Holocene Newer Alluvium aquifers. The potential source of As in sediments carried through the rivers from the Himalayas. Maximum As concentrations in the Older and Newer Alluvium sediments are 13.73 and 30.91 mg/kg, respectively. The Himalayas rivers, i.e. Yamuna, Ganga, Gomati, Ghaghara, Gondak, Buri Gandak, and Kosi rivers carrying suspended sediments have high content of As (max. 10.59 mg/kg).  相似文献   

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