首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 28 毫秒
1.
 The Sanggok mine used to be one of the largest lead-zinc mines in the Hwanggangri mining district, Republic of Korea. The present study characterizes the heavy metal contamination in the abandoned Sanggok mine creek on the basis of physico-chemical properties of various kinds of water samples (mine, surface and groundwater). Hydrochemistry of the water samples is characterized by the relatively significant enrichment of Ca2+, HCO3 –, NO3 – and Cl– in the surface and groundwaters, whereas the mine water is relatively enriched in Ca2+, Mg2+, heavy metals, and HCO3 – and SO4 2–. The more polluted mine water has a lower pH and higher Eh, conductivity and TDS values. The concentrations of some toxic elements (Al, As, Cd, Cu, Fe, Mn, Pb, Se, Sr, Pb and Zn) are tens to hundreds of times higher in the mine water than in the unpolluted surface and groundwaters. However, most immobile toxic pollutants from the mine drainage were quickly removed from the surface water by the precipitation of Al and Fe oxyhydroxides. Geochemical modeling showed that potentially toxic heavy metals might exist largely in the forms of MSO4 2– and M2+ in the mine water. These metals in the surface and groundwaters could form M2+, CO3 2– and OH– complex ions. Computer simulation indicates that the saturation indices of albite, alunite, anhydrite, chlorite, fluorite, gypsum, halloysite and strontianite in the water samples are undersaturated and have progressively evolved toward the saturation condition. However, barite, calcite, chalcedony, dolomite, gibbsite, illite and quartz were in equilibrium, and only clay minerals were supersaturated. Ground and mine waters seemed to be in equilibrium with kaolinite field, but some surface water were in equilibrium with gibbsite and seceded from the stability field of quartz. This indicates that surface water samples in reaction with carbonate rocks would first equilibrate with carbonate minerals, then gibbsite to kaolinite. Investigations on water quality and environmental improvement of the severely polluted Sanggok creek, as well as remediation methods on the possible future pollution of the groundwater by the acid mine drainage from the abandoned metal mines, are urgently required. Received: 4 February 2000 · Accepted: 9 May 2000  相似文献   

2.
A long mining history and unscientific exploitation of Jharia coalfield caused many environmental problems including water resource depletion and contamination. A geochemical study of mine water in the Jharia coalfield has been undertaken to assess its quality and suitability for domestic, industrial and irrigation uses. For this purpose, 92 mine water samples collected from different mining areas of Jharia coalfield were analysed for pH, electrical conductivity (EC), major cations (Ca2+, Mg2+, Na+, K+), anions (F−, Cl−, HCO3 −, SO4 2−, NO3 −), dissolved silica (H4SiO4) and trace metals. The pH of the analysed mine water samples varied from 6.2 to 8.6, indicating mildly acidic to alkaline nature. Concentration of TDS varied from 437 to 1,593 mg L−1 and spatial differences in TDS values reflect the variation in lithology, surface activities and hydrological regime prevailing in the region. SO4 2− and HCO3 − are dominant in the anion and Mg2+ and Ca2+ in the cation chemistry of mine water. High concentrations of SO4 2− in the mine water of the area are attributed to the oxidative weathering of pyrites. Ca–Mg–SO4 and Ca–Mg–HCO3 are the dominant hydrochemical facies. The drinking water quality assessment indicates that number of mine water samples have high TDS, total hardness and SO4 2− concentrations and needs treatment before its utilization. Concentrations of some trace metals (Fe, Mn, Ni, Pb) were also found to be above the desirable levels recommended for drinking water. The mine water is good to permissible quality and suitable for irrigation in most cases. However, higher salinity, residual sodium carbonate and Mg-ratio restrict its suitability for irrigation at some sites.  相似文献   

3.
Geochemical processes that take place in the aquifer have played a major role in spatial and temporal variations of groundwater quality. This study was carried out with an objective of identifying the hydrogeochemical processes that controls the groundwater quality in a weathered hard rock aquifer in a part of Nalgonda district, Andhra Pradesh, India. Groundwater samples were collected from 45 wells once every 2 months from March 2008 to September 2009. Chemical parameters of groundwater such as groundwater level, EC and pH were measured insitu. The major ion concentrations such as Ca2+, Mg2+, Na+, K+, Cl−, and SO4 2− were analyzed using ion chromatograph. CO3 − and HCO3 − concentration was determined by acid–base titration. The abundance of major cation concentration in groundwater is as Na+ > Ca2+ > Mg2+ > K+ while that of anions is HCO3 − > SO4 2− > Cl− > CO3 −. Ca–HCO3, Na–Cl, Ca–Na–HCO3 and Ca–Mg–Cl are the dominant groundwater types in this area. Relation between temporal variation in groundwater level and saturation index of minerals reveals the evaporation process. The ion-exchange process controls the concentration of ions such as calcium, magnesium and sodium. The ionic ratio of Ca/Mg explains the contribution of calcite and dolomite to groundwater. In general, the geochemical processes and temporal variation of groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals.  相似文献   

4.
 A baseline study involving analyses of surface and subsurface water samples from the Akpabuyo area was carried out in order to assess their suitability for drinking, domestic and agricultural purposes. Study results show that the waters are acidic (3.41≤pH≤6.28), soft (hardness 2.09–10.68 mg/l as CaCO3), fresh (conductivity <1400 μs/cm) and characterised by low sodium adsorption ratio, SAR (0.08–0.59). In addition, the mean values of the major cations (Ca2+, Mg2+, Na+, K+) and anions (SO4 2–, Cl–, HCO3 –) are all within the World Health Organisation (WHO) standards. Taking all this into consideration (except pH), the waters may be regarded as excellent for drinking, domestic and agricultural purposes. On the basis of regression equations, the major cations (K, Na, Ca, Mg) correlate well with conductivity. Finally, results also show that four chemical facies are delineated. These include Ca-Cl, Na-Cl, Ca-SO4 and Ca-HCO3. Received: 19 June 1996 / Accepted: 15 April 1997  相似文献   

5.
 Groundwater in alluvial aquifers of the Wakatipu and Wanaka basins, Central Otago, New Zealand, has a composition expressed in equivalent units of Ca2+≫Mg2+≅Na+>K+ for cations, and HCO3 –≫SO4 2->NO3 –≅Cl– for anions. Ca2+ and HCO3 – occur on a 1 : 1 equivalent basis and account for >80% of the ions in solution. However, some groundwater has increased proportions of Na+ and SO4 2-, reflecting a different source for this water. The rock material of the alluvial aquifers of both basins is derived from the erosion and weathering of metamorphic Otago Schist (grey and green schists). Calcite is an accessory mineral in both the grey and green schists at <5% of the rock. Geological mapping of both basins indicates that dissolution of calcite from the schist is the only likely mechanism for producing groundwater with such a constant composition dominated by Ca2+ and HCO3 – on a 1 : 1 equivalent basis. Groundwater with higher proportions of Na+ and SO4 2- occurs near areas where the schist crops out at the surface, and this groundwater represents deeper and possibly older water derived from basement fluids. Anomalously high K+ in the Wakatipu basin and high NO3 – concentrations in the Wanaka basin cannot be accounted for by interaction with basement lithologies, and these concentrations probably represent the influence of anthropogenic sources on groundwater composition. Received, June 1996 Revised, March 1997, July 1997 Accepted, July 1997  相似文献   

6.
The source of fluoride toxicity in Muteh area,Isfahan, Iran   总被引：1，自引：0，他引：1  
Endemic dental fluorosis has been observed in most inhabitants of three villages of Muteh area, located in northwest of Isfahan province, with mottled enamel related to high levels of fluoride in drinking water (1.8–2.2 ppm). Forty-seven groundwater samples from six villages were collected and fluoride concentrations along with physico-chemical parameters were analyzed. Fluoride concentration in this area varies from 0.2 to 9.2 mg/l with highest fluoride level at Muteh gold mine (Chahkhatun mine). Fluoride concentration positively correlates with pH and HCO3 − indicating that alkaline pH provides a suitable condition for leaching of fluoride from surrounding rocks. The district is mainly covered by three lithological units, namely, metamorphic and granite rocks, alluvial sediments, and carbonate rocks. Factor analysis shows that parameters can be classified into four components: electrical conductivity (EC), total dissolved solids (TDS), Cl−, Na+ and K+, pH and F−, SO4 2−and Mg2+, HCO3 − and Ca2 +. The groundwaters from the three geological units were compared using Mann–Whitney U test. The order of median fluoride concentration is: metamorphic and granite rocks > alluvial sediments > carbonate rocks. Hence, the fluoride content is most probably related to fluoride-bearing minerals such as amphibole and mica group minerals in metamorphic and granitic rocks. The concentration of fluoride in drinking water wells located near the metamorphic complex in Muteh area is above 2 ppm.  相似文献   

7.
An integrated study has been carried out to elucidate the distribution and occurrence of arsenic in selected groundwater samples in the area of Sherajdikhan, Bangladesh. Arsenic and other parameters (T, pH, EC, Na+, K+, Ca2+, Mg2+, Cl−, NO3 −, SO4 2−, HCO3 −, PO4 3−, Fe, Mn and DOC) have been measured in groundwater samples collected from shallow/deep tube wells at different depths. Hydrogeochemical data suggest that the groundwaters are generally Ca–Mg–HCO3 and Mg–Ca–HCO3 types with bicarbonate (HCO3 −) as the dominant anion, though the other type of water has also been observed. Dissolved arsenic in groundwater ranged from 0.006 to 0.461 mg/l, with 69% groundwater samples exceeded the Bangladesh limit for safe drinking water (0.05 mg/l). Correlation and principal component analysis have been performed to find out possible relationships among the examined parameters in groundwater. Low concentrations of NO3 − and SO4 2−, and high concentrations of DOC, HCO3 − and PO4 3− indicate the reducing condition of subsurface aquifer where sediments are deposited with abundant organic matter. Distinct relationship of As with Fe and Mn, and strong correlation with DOC suggests that the biodegradation of organic matter along with reductive dissolution of Fe–Mn oxyhydroxides has being considered the dominant process to release As in the aquifers studied herein.  相似文献   

8.
 An integrated geological, geoelectrical and hydrochemical investigation of shallow groundwater occurrence in the Ibadan area, southwestern Nigeria, is presented. The primary objective was to characterise the groundwater in a typical low-latitude environment underlain by Precambrian crystalline basement complex rocks. The dominant rocks comprise suites of gneisses and quartzites. Chemical analyses of the groundwater show that the mean concentration of the cations is in the order Na>Ca>Mg>K while that for the anions is Cl>HCO3>NO3>SO4. Statistical analyses, using the product-moment coefficient of correlation, indicate positive correlations between the following pairs of parameters: TDS and conductivity (r=0.96); Na++Mg2+ and Cl– (r=0.95); Na++K+ and Ca2+ (r=0.43); Na++K+ and HCO3 – (r=0.17); Ca2+ and Mg2+ (r=0.74); Ca2+ and HCO3 – (r=0.33); Ca2++Mg2+ and HCO3 – (r=0.31) and pH and HCO3 – (r=0.54). A very weak negative correlation was recorded between pH and Cl–, with r=–0.003. Five groundwater groups have been identified, namely, (1) the Na-Cl, Na-Ca-Cl, Na-Ca-(Mg)-Cl; (2) the Ca-(Mg)-Na-HCO3-Cl, Na-Ca-HCO3-Cl, and Ca-HCO3-Cl; (3) the Ca-(Mg)-Na-HCO3, Ca-Na-HCO3; (4) Ca-Na-Cl-(SO4)-HCO3 and (5) the Ca-(Mg)-Na-SO4-HCO3. The different groups reflect the diversity of bedrock types and consequently also of the products of weathering. Most of the water sampled is unfit for drinking on account of the high NO3 – content. It can, however, be used for irrigation purposes as the sodium hazard is low while the salinity hazard ranges from low to medium. Resistivity soundings indicate the presence of a thick weathering profile, which could be up to 60 m. Such sites should be the target for any long-term and sustainable groundwater development in the area. Received: 15 April 1998 · Accepted: 4 July 1998  相似文献   

9.
Hydrochemical investigations were carried out in Damagh area, Hamadan, western Iran, to assess chemical composition of groundwater. Forty representative groundwater samples were collected from different wells to monitor the water chemistry of various ions. Chemical analysis of the groundwater showed that the mean concentration of the cations is in the order Na+ > Ca2+ > Mg2+ > K+, while that for anions was HCO3− > Cl− > SO42 − > NO3−. All of the investigated groundwaters present two different chemical facies (Ca–HCO3 and Na–HCO3) which is in relation with their interaction with the geological formations of the basin, cation exchange between groundwater and clay minerals and anthropogenic activities. The principal component analysis (PCA) performed on groundwater identified three principal components controlling their variability in groundwater. Electrical conductivity, Mg2+, Na+, SO42−, and Cl− content were associated in the same component (PC1) (salinity), determined principally by anthropogenic activities. The pH, CO32 −, HCO3−, and Ca2+ (PC2) content were related to the geogenic factor. Finally, the NO3−, Cl− and K+ (PC3) were controlled by anthropogenic activity as a consequence of inorganic fertilizers.  相似文献   

10.
Summary The mineral chemistry of a Variscan lamprophyre (kersantite) from the Frankenwald, Germany, has been investigated by electron microprobe. This potassic, Si-saturated, mafic rock contains an assemblage of different generations of titanite and allanite-(Ce), Th-rich zircon, and metamict REE–Ti–Zr–Th silicates. The primary ferroan-ceroan titanite contains unusually high contents of REE2O3 (max. (ΣLa to Sm)+Y = 36.8 oxide wt.%), ZrO2 (max. 5.4 wt.%), and ThO2 (max. 3.1 wt.%). Its empirical formula averages to (Ca0.31 La0.17 Ce0.30 Pr0.03 Nd0.08 Sm0.01 Y0.01 Fe2+0.06 Th0.02 Mn0.01)Σ1.00 (Ti0.60 Fe2+0.22 Al0.06 Zr0.07 Mg0.04 Nb0.01)Σ1.00 O1.00(Si0.93 Al0.07)Σ1.00 O4. Element correlations reveal operation of the complex substitution Ca2++Ti4++Th4+ ⇔ REE3++Al3++Zr4+. In comparison to allanite-(Ce), ferroan-ceroan titanite preferentially incorporated the LREE and Th. This finding is inconsistent with previous experimental studies and suggests that both minerals are not cogenetic. High Zr contents in titanite, usually known only from Si-undersaturated alkaline rocks, and the predominance of Fe2+ suggest that the ferroan-ceroan titanite crystallized from an alkali-rich, low-fO2 residual melt.  相似文献   

11.
 The environmental conditions prevailing in the Chicam-Toctina drainage system (approx. 138 km2 in Córdoba, Argentina) are considered representative of a number of catchments in Argentina's Sierras Pampeanas Range. Two groups of ions reflect the sources of dissolved species in the catchment: a) a group (Cl–, SO2– 4, and Na+) which recognizes natural and anthropogenic sources, and which exhibits significant correlations with N– 3 and NO– 2, and b) another group of components (Ca2+, Mg2+, and HCO– 3) which is clearly controlled by carbonate rocks and their waste rock products. In the headwaters, stockpiled marble quarry mining wastes provide a more open system to CO2 gaseous exchange than the outcropping rocks, thus promoting the increase of carbonate dissolution (up to 4.88 g km–2 s–1 during the rainy season). This specific yield was 20% higher than the amount estimated for an area with fewer extended mining activities. The dissolved load delivered by the upper reaches is subjected in the lower drainage area to various processes, mainly controlled by the presence of the city of Alta Gracia (approx. 40,000 inhabitants). In the dry season, due to nutrient inputs supplied by the city, photosynthetic activity plays a major role controlling stream pH. Hence, the high values of calcite saturation indexes and the increase of CaCO3 concentration in bed sediments can be explained by calcite precipitation. Such a process could be accompanied by the coprecipitation on calcium carbonate of low solubility heavy metal carbonates. Received : 17 January 1997 · Accepted : 31 March 1997  相似文献   

12.
Pollution of groundwater by seawater intrusion poses a threat to sustainable agriculture in the coastal areas of Korea. Therefore, seawater intrusion monitoring stations were installed in eastern, western, and southern coastal areas and have been operated since 1998. In this study, groundwater chemistry data obtained from the seawater intrusion monitoring stations during the period from 2007 to 2009 were analyzed and evaluated. Groundwater was classified into fresh (<1,500 μS/cm), brackish (1,500–3,000 μS/cm), and saline (>3,000 μS/cm) according to EC levels. Among groundwater samples (n = 233), 56, 7, and 37% were classified as the fresh, brackish, and saline, respectively. The major dissolved components of the brackish and saline groundwaters were enriched compared with those of the fresh groundwater. The enrichment of Na+ and Cl− was especially noticeable due to seawater intrusion. Thus, the brackish and saline groundwaters were classified as Ca–Cl and Na–Cl types, while the fresh groundwater was classified as Na–HCO3 and Ca–HCO3 types. The groundwater included in the Na–Cl types indicated the effects of seawater mixing. Ca2+, Mg2+, Na+, K+, SO4 2−, and Br− showed good correlations with Cl− of over r = 0.624. Of these components, the strong correlations of Mg2+, SO4 2−, and Br− with Cl− (r ≥ 0.823) indicated a distinct mixing between fresh groundwater and seawater. The Ca/Cl and HCO3/Cl ratios of the groundwaters gradually decreased and approached those of seawater. The Mg/Cl, Na/Cl, K/Cl, SO4/Cl, and Br/Cl ratios of the groundwaters gradually decreased, and were similar to or lower than those of seawater, indicating that Mg2+, Na+, K+, SO4 2−, and Br−, as well as Cl− in the saline groundwater can be enriched by seawater mixing, while Ca2+ and HCO3 − are mainly released by weathering processes. The influence of seawater intrusion was evaluated using threshold values of Cl− and Br−, which were estimated as 80.5 and 0.54 mg/L, respectively. According to these criteria, 41–50% of the groundwaters were affected by seawater mixing.  相似文献   

13.
Hydrogeochemical investigations are carried out in the different blocks of Burdwan district, West Bengal, India in order to assess its suitability for drinking as well as irrigation water purpose. Altogether 49 representative groundwater samples are collected from bore wells and the water chemistry of various ions viz. Ca2+, Mg2+, Na+, K+, CO32−, HCO3−, Cl−, SO42− and NO3− are carried out. The chemical relationships in Piper and Gibbs diagram suggest that the groundwater mainly belongs to alkali type and Cl− group and are controlled by rock dominance. A comparison of groundwater quality in relation to drinking water quality standards proves that most of the water samples are suitable for drinking water purpose whereas groundwater in some areas of the district has high salinity and high sodium adsorption ratio (SAR), indicating unsuitability for irrigation water and needs adequate drainage.  相似文献   

14.
Oxygen-18 content and hydrochemistry of the springs issuing from Semmering Massif was intensively monitored with the aim of characterizing the recharge areas and hydrochemical evolution. The δ18O-altitude effect was determined using isotopic and hydrogeological data for small, mainly crystalline reference springs; it was approximated at –0.27 and –0.21‰/100 m respectively for the northern and southern side of the massif. Applying these values the mean recharge altitude of the springs was calculated. For the large-capacity carbonate springs it ranges between 1,100–1,410 m, compatible with the topographic and hydrogeologic frame work of the Mesozoic limestones and dolomites comprised in the Lower Austroalpine feeding the springs. Hydrochemical composition of the carbonate springs is dominated by Ca2+, Mg2+, HCO3 – and SO4 2– ions. With respect to calcite, the springs are nearly saturated, but undersaturated with dolomite (except for some springs that seemed close to saturation). As is typical for carbon dioxide influx from soils in a mountainous region, the mean equilibrium PCO2 is low, within 10–3.0 and 10–2.5 atm (0.1–0.3 vol%). On a long-term scale, the pH and the calculated SIc, SId and equilibrium PCO2 show a strong seasonality, whereas Ca2+, Mg2+ and HCO3 – concentration is almost time invariant. By integrating the results of δ18O and chemical data, altitudinal variability of the chemistry of carbonate groundwater is demonstrated. Reflecting the systematic change of biotic activity and recharge conditions in the catchment areas, a negative co-variation results between the recharge altitude and PCO2 and HCO3 – concentration (HCO3 – is not modified by any source/sink terms, thus rendering the change on the carbonate chemistry). PCO2 and HCO3 – drop by approx. 0.22 log units (atm) and 38.6 mg/l, respectively, for every 100-m gain in recharge altitude. Electronic Publication  相似文献   

15.
A one-dimensional mathematical model based on convection–dispersion equation in unsaturated porous media is presented to compute inorganic total solid concentration in the soil column under the Shiraz landfill. In addition, a dynamic mathematical model is formulated to simulate concentrations of ions such as Ca2+ , Mg2+, Fe2+, K+, Na+, Cl−, SO4 2− and HCO3 − as well as PH and EC in soil profile under the Shiraz landfill. Leachw model was applied to simulate water flow, water content and hydraulic conductivity in soil depth. The model was calibrated and verified by using different sets of data collected from several segments of soil depth in the study area. The numerical solution obtained using finite element method. The simulated values for the parameters were compared with measured values as well as analytical solution. The simulated results are in good agreement with measured values. This model could be applied to field scale problems for the landfill management.  相似文献   

16.
This work reports new hydrochemical data on the two types of cold high p CO2 groundwaters from the Mukhen deposit (Khabarovsk district). The first type is classed with HCO3-Ca-Mg waters with a relatively low TDS (up to 1.7 g/l) and high concentrations of Fe2+, Mn2+, Ba2+, and SiO2. The second type is of HCO3-Na composition with high TDS (up to 14 g/l) and elevated Li+, B, Sr2+, Br?, and I?. New oxygen (δ18O) and hydrogen (δD) isotopic data on the waters and carbon (δ13C) isotopic data on the gas phase, together with a detailed geological and hydrogeological analysis of the study area, allowed us to decipher the origin of both the mineral waters. Based on the tritium content (3H) in the ground and surface waters of the area, the duration of the mineral water circulation was estimated. It was established that the both types of groundwaters were formed during interaction of meteoric water with bedrock under active influence of CO2, however HCO3-Na groundwaters have longer residence time than HCO3-Ca-Mg groundwaters.  相似文献   

17.
The Heihe River Basin is a typical arid inland river basin for examining stress on groundwater resources in northwest China. The basin is composed of large volumes of unconsolidated Quaternary sediments of widely differing grain size, and during the past half century, rapid socio-economic development has created an increased demand for groundwater resources. Understanding the hydrogeochemical processes of groundwater and water quality is important for sustainable development and effective management of groundwater resources in the Heihe River basin. To this end, a total of 30 representative groundwater samples were collected from different wells to monitor the water chemistry of various ions and its quality for irrigation. Chemical analysis shows that water presents a large spatial variability of chemical facies (SO4 2−–HCO3−, SO4 2−–Cl−, and Cl−–SO4 2−) as groundwater flow from recharge area to discharge area. The ionic ratio indicates positive correlation between the flowing pairs of parameters: Cl− and Na+(r = 0.95), SO4 2− and Na+ (r = 0.84), HCO3 − and Mg2+(r = 0.86), and SO4 2− and Ca2+ (r = 0.91). Dissolution of minerals, such as halite, gypsum, dolomite, silicate, and Mirabilite (Na2SO4·10H2O) in the sediments results in the Cl−, SO4 2−, HCO3 −, Na+, Ca2+ and Mg2+ content in the groundwater. Other reactions, such as evaporation, ion exchange, and deposition also influence the water composition. The suitability of the groundwater for irrigation was assessed based on the US Salinity Laboratory salinity classification and the Wilcox diagram. The results show that most of the groundwater samples are suitable for irrigation uses barring a few locations in the dessert region in the northern sub-basin.  相似文献   

18.
This paper reports original data on the physical and chemical parameters of precipitation, river water and groundwater in and around the Longhushan Nature Reserve Area, located in southwestern China karst region, and provides a preliminary characterization of the hydrogeochemical process governing the natural water evolution in this area. The rainfall and river water mainly pertain to the HCO3 −–Ca2+ type and groundwater mainly pertain to the HCO3 −–Ca2+ + Mg2+ type. The HCO3 − was the predominant anion and Ca2+ was the predominant cation in all waters, respectively. The Gibbs Boomerang Envelop model, the 1:1 relationship of Na+ plus K+ versus Cl− as well as the 1:1 relationship of Ca2+ plus Mg2+ versus HCO3 − all suggested geochemical weathering is the main controlling factor for the geochemical compositions of this natural water. In surface water, the Mg2+/Ca2+ ratios ranged from 0.32 to 0.42 and the Na+/Ca2+ varied between 0.04 and 0.05. In the groundwater, the Mg2+/Ca2+ ratios varied from 0.37 to 0.62 and were below the ideal ratio of 0.8. These ratios showed the presence of a dolomite source. Analysis of trace elements showed that As, B, Pb, Se, Sr, V and Zn elements were abundant in the natural water during summer in this region.  相似文献   

19.
Phase transformations in a natural sample of hedenbergite ((Ca0.93Fe0.61Mn0.34Mg0.08Na0.01Zn0.02Al0.003)Si2O6) have been studied by X-ray diffraction up to 40 GPa at ∼ 1200°C in a diamond anvil cell interfaced with a laser heating system. The starting hedenbergite phase decomposed into a garnet plus γ-spinel and stishovite at ∼ 14 GPa; then into garnet plus stishovite and wüstite at ∼ 18 GPa; and finally into perovskite plus stishovite and wüstite at pressures higher than ∼ 24 GPa. On decompression to 0.1 MPa, all the high pressure phases are retained except for the cubic perovskite, which reverts back into the ɛ-CaSiO3 phase, in accordance with previous reports. Energy-dispersive SEM analyses show that the garnet is present as a calcium-rich ABO 3-type phase. As no garnet phase has been previously observed either in pure CaSiO3 or in pure CaMgSi2O6, it appears that the observed calcium-rich garnet phase has been stabilized by the presence of other cations such as the Na+, Zn2+, Mn2+, Fe2+, Mn3+, Fe3+ and Al3+.  相似文献   

20.
Muzaffarnagar is an economically rich district situated in the most fertile plains of two great rivers Ganga and Yamuna in the Indo-gangetic plains, with agricultural land irrigated by both surface water as well as groundwater. An investigation has been carried out to understand the hydrochemistry of the groundwater and its suitability for irrigation uses. Groundwater in the study area is neutral to moderately alkaline in nature. Chemistry of groundwater suggests that alkaline earths (Ca + Mg) significantly exceed the alkalis (Na + K) and weak acids exceed the strong acids (Cl + SO4), suggesting the dominance of carbonate weathering followed by silicate weathering. Majority of the groundwater samples (62%) posses Ca–Mg–HCO3 type of hydrochemical species, followed by Ca–Na–Mg–HCO3, Na–Ca–Mg–HCO3, Ca–Mg–Na–HCO3–Cl and Na–Ca–HCO3–SO4 types. A positive high correlation (r 2 = 0.928) between Na and Cl suggests that the salinity of groundwater is due to intermixing of two or more groundwater bodies with different hydrochemical compositions. Barring a few locations, most of the groundwater samples are suitable for irrigation uses. Chemical fertilizers, sugar factories and anthropogenic activities are contributing to the sulphate and chloride concentrations in the groundwater of the study area. Overexploitation of aquifers induced multi componential mixing of groundwater with agricultural return flow waters is responsible for generating groundwater of various compositions in its lateral extent.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号