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 57 毫秒
1.
Reservoir fluid compositions have been assessed from analytical data on water samples collected from thermal and cold waters in Balçova geothermal field. The results of mineral equilibrium modelling indicate that the waters, with some exceptions, are systematically supersaturated with respect to calcite, aragonite, dolomite, chalcedony and quartz, but undersaturated with respect to amorphous silica, celestite, anhydrite and gypsum and undersaturated or supersaturated with respect to barite, low-albite, K-feldspar, gibbsite and Fe(OH)3(a). Calculation of mineral saturation states and geochemical analyses of scale and field observations show that carbonate minerals (calcite, aragonite and dolomite) are most likely to be precipitated as a scale type. Besides carbonates, scale formation risk of amorphous silica, Fe(OH)3(a), anhydrite, barite and celestite minerals should be taken into account in some wells and surface equipment. Most of the waters, with some exceptions, have carbonate scaling risk at all temperatures, whereas the other scaling risks only exist over a limited temperature range. While silica, Fe(OH)3(a) and barite show a scaling tendency at low temperatures, anhydrite and celestite scaling occurs at higher temperatures.  相似文献   

2.
The previous study showed that the Zechstein (Upper Permian) anhydrites have about 0.2% strontium with a remarkably small sample scatter. Our study of three lower Zechstein anhydrite units (Lower Anhydrite, Upper Anhydrite and Basal Anhydrite) from West Poland indicate that although often the Sr content is 0.1–0.2%, there are common deviations. In particular, a considerable part (28%) of the studied samples is characterized by lower values (<0.1%), and on the other hand ca. 15% of samples are Sr-enriched, and in those samples celestite was recorded. Particular anhydrite levels differ especially in the frequency of samples showing great Sr content. The greatest variation was found in the Lower Anhydrite. This agrees well with the conclusion derived from the sedimentological studies indicating that there was the greatest differentiation of depositional environments during the deposition of the Lower Anhydrite. The Sr content is a good indicator of brine concentration during the gypsum precipitation and it seems that the subsequent gypsum–anhydrite transformation itself does not affect the strontium distribution. The histograms of Sr content in the Basal Anhydrite indicate a slightly higher brine concentration than it was during the Lower Anhydrite deposition, and the latter in turn was higher than brine concentration during the Upper Anhydrite sedimentation. Celestite veins are clearly diagenetic in origin. The form of celestite occurrence and the increased strontium content (1% or more) indicate an additional source of ions that occurred outside the anhydrite series. In the case of the Lower Anhydrite, the supposed additional source of Sr was related to aragonite-to-calcite transition and squeezing of CaCl2 brines from reefs into anhydrite series due to increased pressure. For the Basal Anhydrite this source could be related to brines derived from the Older Halite deposits.  相似文献   

3.
Sabkhas are ubiquitous geomorphic features in eastern Saudi Arabia. Seven brine samples were taken from Sabkha Jayb Uwayyid in eastern Saudi Arabia. Brine chemistry, saturation state with respect to carbonate and evaporate minerals, and evaporation-driven geochemical reaction paths were investigated to delineate the origin of brines and the evolution of both brine chemistry and sabkha mineralogy. The average total dissolved solids in the sabkha brines is 243 g/l. The order of cation dominance is Na+   >>  Mg2+ >>  Ca2+>K+, while anion dominance is Cl− >> SO4 2− >> HCO3 −. Based on the chemical divide principle and observed ion ratios, it was concluded that sabkha brines have evolved from deep groundwater rather than from direct rainfall, runoff from the surroundings, or inflow of shallow groundwater. Aqueous speciation simulations show that: (1) all seven brines are supersaturated with respect to calcite, dolomite, and magnesite and undersaturated with respect to halite; (2) three brines are undersaturated with respect to both gypsum and anhydrite, while three brines are supersaturated with respect to both minerals; (3) anhydrite is a more stable solid phase than gypsum in four brines. Evaporation factors required to bring the brines to the halite phase boundary ranged from 1.016 to 4.53. All reaction paths to the halite phase boundary follow the neutral path as CO2 is degassed and dolomite precipitates from the brines. On average, a sabkha brine containing 1 kg of H2O precipitates 7.6 g of minerals along the reaction path to the halite phase boundary, of which 52% is anhydrite, 35.3% is gypsum, and 12.7% is dolomite. Bicarbonate is the limiting factor of dolomite precipitation, and sulfate is the limiting factor of gypsum and anhydrite precipitation from sabkha brines.  相似文献   

4.
226Ra, 228Ra and Ba distributions as well as 228Ra/226Ra and 226Ra/Ba ratios were measured in seawater, suspended and sinking particles at the DYFAMED station in the Western Mediterranean Sea at different seasons of year 2003 in order to track the build-up and fate of barite through time. The study of the 228Raex/226Raex ratios (Raex = Ra activities corrected for the lithogenic Ra) of suspended particles suggests that Baex (Baex = Ba concentrations corrected for the lithogenic Ba, mostly barite) formation takes place not only in the upper 500 m of the water column but also deeper (i.e. throughout the mesopelagic layer). Temporal changes in the 228Raex/226Raex ratios of sinking particles collected at 1000 m depth likely reflect changes in the relative proportion of barite originating from the upper water column (with a high 228Ra/226Ra ratio) and formed in the mesopelagic layer (with a low 228Ra/226Ra ratio). 228Raex/226Raex ratios measured in sinking particles collected in the 1000 m-trap in April and May suggest that barite predominantly formed in the upper water column during that period, while barite found outside the phytoplankton bloom period (February and June) appears to form deeper in the water column. Combining ratios of both the suspended and sinking particles provides information on aggregation/disaggregation processes. High 226Raex/Baex ratios were also found in suspended particles collected in the upper 500 m of the water column. Because celestite is expected to be enriched in Ra [Bernstein R. E., Byrne R. H. and Schijf J. (1998) Acantharians: a missing link in the oceanic biogeochemistry of barium. Deep-Sea Res. II45, 491-505], acantharian skeletons may contribute to these high ratios in shallow waters. The formation of both acantharian skeletons and barite enriched in 226Ra may thus contribute to the decrease in the dissolved 226Ra activity and 226Ra/Ba ratios of surface waters observed between February and June 2003 at the DYFAMED station.  相似文献   

5.
The enthalpy, Gibbs free energy, and entropies of aqueous radium species and radium solids have been evaluated from empirical data, or estimated when necessary for 25°C and 1 bar. Estimates were based on such approaches as extrapolation of the thermodynamic properties of Ca, Sr, and Ba complexes and solids plotted against cationic radii and charge to radius functions, and the use of the Fuoss or electrostatic mathematical models of ion pair formation (Langmuir, 1979). Resultant log K (assoc) and ΔH0 (assoc) (kcal/mol) values are: for RaOH+ 0.5 and 1.1; RaCl+ ?0.10 and 0.50; RaCO03 2.5 and 1.07; and RaSO04 2.75 and 1.3. Log Ksp and ΔH0 (dissoc) (kcal/mol) values for RaCO3(c) and RaSO4(c) are ?8.3 and ?2.8, and ?10.26 and ?9.4, respectively.Trace Ra solid solution in salts of Pb and of the lighter alkaline earths, has been appraised based on published distribution coefficient (D) data, where D ～- (mM2+)(NRaX)/(mRa2+)(NMX) (m and N are the aqueous molality and mole fraction of Ra and cation M in salt X, respectively. The empirical solid solution data have been used to derive both enthalpies and Gibbs free energies of solid solution of trace Ra in sulfate and carbonate minerals up to 100°C. Results show that in every case D values decrease with increasing temperature. Among the sulfate and carbonate minerals, D values decrease for the following minerals in the order: anhydrite > celestite > anglesite > barite > aragonite > strontianite > witherite > cerussite.  相似文献   

6.
The composition of waters from 10 thermal springs located in western Virginia near the 38th parallel lineament have been analysed for major dissolved components and for Sr, Fe, Cu, Zn and Cd; from these analyses, free ion activities have been calculated. The temperatures of the springs range from 17° to 39°C, the heat apparently being derived simply from deep circulation along synclinal, Middle Ordovician limestones. More than 95 per cent of the dissolved solids consist of Ca2+, Mg2+ HCO3?, and SO42?. The concentrations of these components, as well as the spring temperatures, have not changed appreciably in 140 yr in some springs. The waters that have temperatures below 25° are all undersaturated with respect to calcite and dolomite, possibly because they have been contaminated by shallow ground waters. The waters with temperatures above 25° are in equilibrium with calcite and dolomite. Furthermore, in this latter group, the calcium-sulfate activity product and the sulfate-carbonate activity ratio are nearly constant, even though the waters are under saturated with respect to gypsum, anhydrite, celestite and strontianite. This can be explained if CaSO4 is coprecipitated in a mineral such as aragonite. The waters have absorbed some dissolved oxygen near the surface, but at depth they may be anoxic with Eh controlled by the oxidation of pyrite to goethite. The extremely low chloride concentrations of these waters clearly distinguish them from the brines which deposited Mississippi Valley and Appalachian type epithermal ore deposits.  相似文献   

7.
《Chemical Geology》1999,153(1-4):187-209
This paper describes a model for barite and celestite solubilities in the Na–K–Ca–Mg–Ba–Sr–Cl–SO4–H2O system to 200°C and to 1 kbar. It is based on Pitzer's ion interaction model for the thermodynamic properties of the aqueous phase and on values of the solubility products of the solids revised in this work. It is shown how barite and celestite solubilities in electrolyte solutions can be accurately predicted as a function of temperature and pressure from previously determined Pitzer's parameters. The equilibrium constant for the BaSO4(aq) ion pair dissociation reaction is calculated from recently reported barite solubility in Na2SO4 solutions from 0 to 80°C. Pressure corrections are evaluated through partial molal volume calculations and are partially validated by comparing model predictions to measured barite and celestite solubilities in pure water to 1 kbar and in NaCl solutions to 500 bars. The model is then used to investigate the tendency of ion pairing of Ca, Sr and Ba with sulfate in seawater. Finally, the activity coefficient of aqueous barium sulfate in seawater is calculated for temperature, pressure and salinity values found in the ocean and compared to published values.  相似文献   

8.
This study was conducted to define the geochemical controls on 226Ra during raffinate (pH = 1.2) neutralization to pH 10 at the Key Lake U mill in northern Saskatchewan, Canada. High activities (120–150 Bq/L) of aqueous phase 226Ra are present in raffinate produced during milling of U ore. The solubility control of 226Ra in the SO4-rich, hydrometallurgical raffinate solutions often involves the addition of BaCl2 to form a radium-barite co-precipitate (Ba(Ra)SO4). As such, neutralization experiments were conducted with samples of mill raffinate using Ca(OH)2 or NaOH with and without the addition of BaCl2. Radium-226 activity decreased from 150 to <4 Bq/L for all combinations of neutralizing agents with Ca(OH)2 + BaCl2 being the most effective combination (final activity ∼1.0 Bq/L; ∼99.3% removal). In the absence of BaCl2, Ca(OH)2 more efficiently removed 226Ra than NaOH between pH 4 and 8, due to the co-precipitation of 226Ra with gypsum. Overall, neutralization with the addition of BaCl2 reduced 226Ra activities at lower pH values (by pH 4.5), due to co-precipitation of 226Ra with BaSO4. At varying concentrations of BaCl2, aqueous phase activities of 226Ra converged, but did not attain steady-state values during neutralization and would continue to decrease with time. Sequential extractions indicated that 226Ra in precipitates formed during neutralization of the mill raffinate is dominated by amorphous and crystalline Fe hydroxide phases, consistent with raffinate neutralization experiments that showed that adsorption onto ferrihydrite can remove most 226Ra in the raffinate. Data generated in this study are being used to define the long-term geochemical controls on 226Ra in U mill processes and tailings.  相似文献   

9.
Coprecipitation of barite with trace constituents was simulated with consideration of aqueous speciation and complexation, mixing properties for the binary solid solutions (Zhu, this issue), precipitation and dissolution kinetics, and advective-dispersive transport. Speciation-solubility modeling was used to reproduce BaSO4-RaSO4 coprecipitation experimental results, and to calculate CrO42− aqueous concentrations in equilibrium with a Ba(SO4,CrO4) solid solution. Kinetic reaction path modeling was used to simulate the coprecipitation of barite with RaSO4 to form an onion-like chemically zoned solid upon the cooling of oil field brine.A one-dimensional coupled reactive mass transport model shows a strikingly different transport pattern for the tracer Ra2+, when the dominant attenuation reaction is with solid solution (Ba, Ra) SO4 as compared to the case when it is controlled by pure RaSO4 and barite solids under local equilibrium conditions. A self-enrichment of Ra2+ in the groundwater and aquifer solid matrix—higher concentrations of Ra2+ downstream from the reaction front—results from the coprecipitation reaction and advective-dispersive transport. This self-enrichment process generates a secondary tracer source, which has tracer concentrations higher than that of the original source. On the other hand, coprecipitation reactions can reduce Ra2+ concentrations in groundwater to a much lower level (below ppb) than that of pure RaSO4(c) solubility (near ppm), which has been used to establish the Ra2+ concentration limits in groundwater, soil, and nuclear waste repositories.  相似文献   

10.
《Applied Geochemistry》2003,18(7):1095-1110
The exchange of 226Ra and trace metals across the tailings-water interface and the mechanisms governing their mobility were assessed via sub-centimetre resolution profiling of dissolved constituents across the tailings–water interface in Cell 14 of the Quirke Waste Management Area at Rio Algom's Quirke Mine, near Elliot Lake, Ontario, Canada. Shallow zones (<1.5 m water depth) are characterized by sparse filamentous vegetation, well-mixed water columns and fully oxygenated bottom waters. Profiles of dissolved O2, Fe and Mn indicate that the tailings deposits in these areas are sub-oxic below tailings depths of ∼3 cm. These zones exhibit minor remobilization of Ra in the upper 5 cm of the tailings deposit; 226Ra fluxes at these sites are relatively small, and contribute negligibly to the water column activity of 226Ra. The shallow areas also exhibit minor remobilization of Ni, As, Mo and U. The release of these elements to the water cover is, however, limited by scavenging mechanisms in the interfacial oxic horizons. The presence of thick vegetation (Chara sp.) in the deeper areas (>2 m water depth) fosters stagnant bottom waters and permits the development of anoxia above the benthic boundary. These anoxic tailings are characterized by substantial remobilization of 226Ra, resulting in a relatively large flux of 226Ra from the tailings to the water column. The strong correlation between the porewater profiles of 226Ra and Ba (r2=0.99), as well as solubility calculations, indicate that the mobility of Ra is controlled by saturation with respect to a poorly ordered and/or impure barite phase [(Ra,Ba)SO4]. In the anoxic zones, severe undersaturation with respect to barite is sustained by microbial SO4 reduction. Flux calculations suggest that the increase in 226Ra activity in the water cover since 1995 (from <0.5 to 2.5 Bq l−1) can be attributed to an increase in the spatial distribution of anoxic bottom waters caused by increased density of benthic flora. The anoxic, vegetated areas also exhibit minor remobilization with respect to dissolved As, Ni and Zn. The removal of trace metals in the anoxic bottom waters appears to be limited by the availability of free sulphide. Collectively, the data demonstrate that while the water cover over the U mill tailings minimizes sulphide oxidation and metal mobility, anoxic conditions which have developed in deeper areas have led to increased mobility of 226Ra.  相似文献   

11.
Electron paramagnetic resonance (EPR) measurements of natural anhydrite CaSO4, celestite SrSO4 and barite BaSO4 have revealed the presence of PO 3 2? and SO 3 ? radicals. Hyperfine structure from33S has been detected and measured for the first time. Low-symmetry effects, which are manifested in noncoincidence of g and hyperfine axes, were observed for SO 3 ? . The dynamics of one of the two SO 3 ? types in anhydrite has been investigated. Variations of spin Hamiltonian parameters with temperature have been attributed to thermally induced jumps between the two magnetically inequivalent sites of this center.  相似文献   

12.
Thermodynamic numerical simulations were carried out to determine the principal simple and complex migration species of Ca, Mg, Na, K, Al, B, Mn, Mo, Sr, and U with Cl–, OH–, SO4?2, HCO3?, and CO32? in waters at the Lomonosov diamond deposit and to estimate the saturation indexes with respect to kaolinite, Na- and Mg-montmorillonite, Mg- and Na-saponite, muscovite and paragonite, biotite, phlogopite, chromite, pyrite, plagioclase (anorthite, labradorite, and andesine), olivine (forsterite and fayalite), diopside, pyrope, gypsum, anhydrite, barite, magnesite, calcite, dolomite, talc, chrysotile, chlorite, goethite, quartz, microcline, and albite. The waters are proved not to be saturated with respect to the primary (hydrothermal) minerals. The saturation of certain water samples with uranophane suggests that this mineral is of secondary genesis. The ascent of highly mineralized deep waters shall result in the dissolution of minerals whose concentrations are near the saturation ones. To maintain the ecological standards of the discharged waters, they should be diluted and/or purified by adsorbing dissolved U on a reducing reactive barrier.  相似文献   

13.
The Emet basin is one of the Neogene basins in western Turkey containing significant amounts of borate minerals, mainly colemanite. The petrologic study of core samples from two exploratory wells in the Do?anlar sector, under optic and electron microscopy, reveals a complex mineral association in which probertite, glauberite, and halite constitute the major primary phases (without mineral precursors) precipitated in a saline lake placed in a volcano-sedimentary context. Other sulfates (anhydrite, gypsum, thenardite, celestite and kalistrontite), borates (colemanite, ulexite, hydroboracite, tunellite, kaliborite and aristarainite), and sulfides (arsenopyrite, realgar and orpiment) are attributed to early diagenesis. So far, the Do?anlar deposit is the most important deposit of probertite known up to now.Chemical changes in the groundwater inflow led to the precipitation of Ca-bearing borates (colemanite) in the tuff-flat environment surrounding the lake, while Na–Ca sulfates and borates (glauberite and probertite) precipitated in the center of the lake. Fluid inclusion compositions in halite indicate that the advanced brines correspond to the Na-K-Cl-SO4 type. During restricted stages of the saline lake, the residual brines seeped through the tuff-flat sediments, leading to transformations of previous precipitates that resulted in the formation of K-bearing minerals.The abundance of coccoid-like biogenic dolomite, colloidal arsenopyrite and the isotopic composition of sulfates are indicative of bacterial sulfate reduction. In contrast, arsenic sulfides are attributed to acidophilic micro-organisms in oxidizing conditions. Fluctuations of redox conditions in both free and interstitial brines control the biological influence in some diagenetic transformations.  相似文献   

14.
Crystals of synthetic barite (BaSO4), celestite (SrSO4), and their solid solutions were recrystallized from brine by thermal cycling. Electron probe microanalyses show that the solid solutions are homogeneous within detection limits. The molar composition of solid solution crystals approximates the ideal value based on the ratio of equilibrium constants for barium and strontium sulfates.  相似文献   

15.
《Applied Geochemistry》2001,16(1):109-122
The purpose of this study was to elucidate the processes controlling the distribution and behavior of the longer-lived Ra isotopes in continuous Paleozoic carbonate aquifers of parts of Missouri, Kansas, and Oklahoma. Activities of (228Ra) and (226Ra) were analyzed in fresh and saline ground waters, brines, and rocks. The fluids have a wide salinity range (200–250,000 mg l−1 total dissolved solids). The (226Ra) activity ranges from 0.66–7660 dpm kg−1 and correlates with salinity and other alkaline earth element (Ca, Sr, and Ba) concentrations. The range of (228Ra:226Ra) ratios in the fluids (0.06–1.48) is similar to that in the aquifer rocks (0.21–1.53). The relatively low mean fluid (228Ra:226Ra) ratio (0.30) reflects the low Th:U ratio of the predominant carbonate aquifer rock. Radium occurs mostly (≥77%) as Ra2+ species in the fluids. Salinity-dependent sorption–desorption processes (with log K values from 100–104 and negatively correlated with salinity), involving Th-enriched surface coatings on aquifer flow channels, can explain the rapid solid–fluid transfer of Ra isotopes in the system and the correlation of Ra with salinity.  相似文献   

16.
The intrinsic luminescence center (LC) of SO 4 2? appears at 360 nm in all types of sulfates, but is absent in sulfates with large quantities of impurities. Three nonequivalent Gd3+ LC have been observed in luminescence spectra of anhydrite. Gd3+, Ce3+ O 2 ? LC were established in celestite. Photoluminescence (PL) bands in the sulfates were assigned as follows: the band at 460 nm is related to Eu2+ (a connection with Al3+ or donor-acceptor pair is possible also) in sulfates of Ca and Ba; bands at 520 nm and 590 nm are related to VO4, MoO4 and TiO4 substituting SO4; the band at 660 nm is assigned to Ti3+ X-ray luminescence (XL) band at 620 nm is assigned to Ag+.  相似文献   

17.
Two samples of produced-water collected from a storage tank at US Geological Survey research site B, near Skiatook Lake in northeastern Oklahoma, have activity concentrations of dissolved 226Ra and 228Ra that are about 1500 disintegrations/min/L (dpm/L). Produced-water also contains minor amounts of small (5–50 μm) suspended grains of Ra-bearing BaSO4 (barite). Precipitation of radioactive barite scale in the storage tank is probably hindered by low concentrations of dissolved SO4 (2.5 mg/L) in the produced-water. Sediments in a storage pit used to temporarily collect releases of produced-water have marginally elevated concentrations of “excess” Ra (several dpm/g), that are 15–65% above natural background values. Tank and pit waters are chemically oversaturated with barite, and some small (2–20 μm) barite grains observed in the pit sediments could be transferred from the tank or formed in place. Measurements of the concentrations of Ba and excess Ra isotopes in the pit sediments show variations with depth that are consistent with relatively uniform deposition and progressive burial of an insoluble Ra-bearing host (barite?). The short-lived 228Ra isotope (half-life = 5.76 a) shows greater reductions with depth than 226Ra (half-life = 1600 a), that are likely explained by radioactive decay. The 228Ra/226Ra activity ratio of excess Ra in uppermost pit sediments (1.13–1.17) is close to the ratio measured in the samples of produced-water (0.97, 1.14). Declines in Ra activity ratio (excess) with sediment depth can be used to estimate an average rate of burial of 4 cm/a for the Ra-bearing contaminant. Local shallow ground waters contaminated with NaCl from produced-water have low dissolved Ra (<20 dpm/L) and also are oversaturated with barite. Barite is a highly insoluble Ra host that probably limits the environmental mobility of Ra at site B.  相似文献   

18.
We measured 228Raex/226Raex and 226Raex/Baex ratios in suspended and sinking particles collected at the Oceanic Flux Program (OFP) time-series site in the western Sargasso Sea and compared them to seawater ratios to provide information on the origin and transport of barite (BaSO4) in the water column. The 228Raex/226Raex ratios of the suspended particles down to 2000 m are nearly identical to those of seawater at the same water depth. These ratios are much lower than expected if suspended barite was produced in surface waters and indicate that barite is produced throughout the mesopelagic layer. The 228Raex/226Raex activity ratios of sinking particles collected at 1500 and 3200 m varied mostly between 0.1 and 0.2, which is intermediate between the seawater ratio at these depths (<0.03) and the seawater ratios found in the upper 250 m (0.31-0.42). This suggests that excess Ba (i.e., Baex = Batotal − Balithogenic), considered to be mainly barite, present in the sinking flux is a mixture of crystals formed recently in the upper water column, formed several years earlier in the upper water column, or formed recently in deeper waters. We observe a sizeable temporal variability in the 228Raex/226Raex ratios of sinking particles, which indicates temporal variability in the relative proportion of barite crystals originating from surface (with a high 228Raex/226Raex ratio) and mesopelagic (with a low 228Raex/226Raex ratio) sources. However, we could not discern a clear pattern that would elucidate the factors that control this variability. The 226Ra/Ba ratios measured in seawater are consistent with the value reported from the GEOSECS expeditions (2.3 dpm μmol−1) below 500 m depth, but are significantly lower in the upper 500 m. High 226Raex/Baex ratios and elevated Sr concentrations in suspended particles from the upper water column suggest preferential uptake of 226Ra over Ba during formation of SrSO4 skeletons by acantharians, which must contribute to barite formation in shallow waters. Deeper in the water column the 226Raex/Baex ratios of suspended particles are lower than those of seawater. Since 228Raex/226Raex ratios demonstrate that suspended barite at these depths has been produced recently and in situ, their low 226Raex/Baex ratios indicate preferential uptake of Ba over Ra in barite formed in mesopelagic water.  相似文献   

19.
Groundwater constitutes the main source of water supply in the High Mekerra watershed of northwestern Algeria. This resource is currently under heavy pressures to meet the growing needs of drinking water and irrigation. This study assesses the geochemical characteristics of groundwater of the High Mekerra watershed at 21 points distributed across the two main aquifers (Ras El Ma and Mouley Slissen) in the region. Hydrochemical facies of Ras El Ma groundwater are dominantly MgCl and CaCl type, while those of Mouley Slissen groundwater are of CaHCO3 type. Principal component analysis shows a strong correlation between groundwater mineralization and Ca2+, Na+, Cl? and SO4 2? ions stemming from the dissolution of carbonates, gypsum and anhydrite. Groundwater mineralization evolves from south to north. Geochemical modeling shows that the High Mekerra groundwater is saturated with respect to calcite and dolomite and undersaturated with respect to gypsum and anhydrite. Nitrate concentrations that exceed the WHO standard (50 mg L?1) at several points are linked to the agro-pastoral activities in this region.  相似文献   

20.
《Chemical Geology》2006,225(3-4):266-277
  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