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1.
Pervasive carbonatization of metabasalts is characteristic of many large gold-producing regions such as the Timmins district. Weight per cent CO2 however, does not readily identify specific potential gold-bearing targets. Molar CO2/CaO ratios, which reflect proportions of calcite and dolomite, and ppm arsenic are somewhat more effective than weight per cent CO2. The most effective indicator of gold mineralization is provided by a discriminant function involving both molar CO2/CaO and As.  相似文献   

2.
In the present study, the waste coral was utilized as a source of calcium oxide for transesterification of soybean oil into biodiesel (methyl esters). Characterization results revealed that the main component of the waste coral is calcium carbonate which transformed into calcium oxide when calcined above 700 °C. The Box–Behnken design of experiment was carried out, and the results were analyzed using response surface methodology. Calcination temperature, methanol– soybean oil molar ratio and catalyst concentration were chosen as variables. The methyl ester content (wt%) was response which must be maximized. A second-order model was obtained to predict methyl ester content as a function of these variables. Each variable was placed in the three low, medium and high levels (calcination temperature of 700, 800 and 900 °C; catalyst concentration of 3, 6 and 9 wt%; methanol-to-oil ratios of 12:1, 18:1 and 24:1). The optimum conditions from the experiment were found that the calcination temperature of 900 °C, catalyst concentration of 6 wt% and methanol-to-oil ratio of 12:1. Under these conditions, methyl ester content reached to 100 wt%. The waste catalyst was capable of being reused up to 4 times without much loss in the activity.  相似文献   

3.
Health hazards from heavy metal pollution in water systems are a global environmental problem. Of similar concern is sludge that results from wastewater treatment due to unsatisfactory sludge management technology. Therefore, the effectiveness of using Mg–Al-layered double hydroxide in the removal of heavy metals from mine wastewater was tested and compared with that of calcium hydroxide [Ca(OH)2], which is a common treatment method for heavy metal removal. Initially, the mine wastewater contained cations of the heavy metals iron (Fe), zinc (Zn), copper (Cu), and lead (Pb). The Mg–Al-layered double hydroxides were able to remove 371, 7.2, 121, and 0.4 mg/L of these pollutants, respectively, using the co-precipitation method. The removal of these metals is most effective using 0.5 g Mg–Al-layered double hydroxide (Mg/Al molar ratio 4) and 20 min of shaking. Zn was removed by the formation of Zn(NO3)(OH)·H2O and Zn5(NO3)2(OH)8 when LDH, Mg/Al molar ratios of 4 and 2, respectively, were used. Similarly, Fe, Cu, and Pb were removed by the formation of Fe–Al-layered double hydroxide, Cu2(OH)3·NO3 and Pb4(OH)4(NO3)4, respectively. While Ca(OH)2 is also capable of reducing the heavy metal concentrations below the Japanese recommended values, this analysis shows that using 0.5 g Mg–Al-layered double hydroxide is a better treatment condition for mine wastewater, because it generates lower sludge volumes than 0.1 g of Ca(OH)2. The measured sludge volume was 1.5 mL for Mg–Al-layered double hydroxide and 2.5 mL for Ca(OH)2, a nearly twofold further reduction.  相似文献   

4.
Red mud (RM) was produced during alumina production from bauxite known as the Bayer process. Arsenic was detected in the solid phase of RM (RMsf) which was disposed in the disposal area. This study investigates the effectiveness of using Zero-valent iron (ZVI), ferrihydrite, ferrous sulfate (FeSO4), waste acid (WA) or CO2 for immobilization of arsenic in the RMsf. To test the effect of the amendments on the arsenic leachability, the RMsf samples were amended with the iron-based materials or acidifiers at various w/w (weight/weight) ratios (1–10 %) for 30 days. The leachability of arsenic in the RMsf was evaluated by a 4-step water elusion process. After 30-day treatment of the RMsf, the leachability of As decreased from an initial (12.7 %) to (7.0 %) with a w/w ratio of 5 % ZVI (0 %) with 5 % FeSO4·7H2O, (3.4 %) with 5 % ferryhydrite, (2.0 %) with 6 % WA and (11.8 %) with 6 % CO2. FeSO4·7H2O and WA showed more effectively than other amendments for immobilizing arsenic. Arsenic fractionation with a sequential extraction procedure was used to evaluate the arsenic migration potential in the RMsf. FeSO4 and WA were effective in increasing the hydrous oxide combined arsenic in the RMsf. The leachable Cl? and SO4 2? in the RMsf increased from 2.9 to 14.1 mg/g and 19.9–44.4 mg/g with 6 % WA and 5 % FeSO4·7H2O added, respectively. The estimated cost of the FeSO4 and WA treatment was 0.47 and 0.49 USD per ton, respectively.  相似文献   

5.
The reuse of waste materials as soil additives could be a welcome development in soil remediation. The mobility of Cd, Pb and As in a contaminated soil was investigated using natural and calcined poultry wastes (eggshell and chicken bone), CaCO3 and CaO at different application rates (0, 1, 3 and 5 %). The chemical composition accompanied with mineralogical composition indicated that CaCO3 and CaO were the major components in natural and calcined eggshells, respectively, while hydroxyapatite (HAP) dominated the natural and calcined chicken bones. The results showed that soil pH tended to increase in response to increasing application rates of all soil additives. The effectiveness of the additives in reducing Cd, Pb and As mobility was assessed by means of chemical extractions with 0.1 N HCl for Cd and Pb or 1 N HCl for As, according to Korean Standard Test (KST) method. Both calcined eggshell and chicken bone were equally effective with CaO or CaCO3 in reducing the concentration of 0.1 N HCl-extractable Cd from 6.17 mg kg?1 to below warning level of 1.5 mg kg?1, especially at the highest application rate. The application of calcined eggshell, CaO and CaCO3 also decreased the concentration of 0.1 N HCl-extractable Pb from 1,012 mg kg?1 to below warning level of 100 mg kg?1. The Pb concentration decreased significantly with an increasing application rate of chicken bone, but remained above warning level even at the highest application rate. On the contrary, natural and calcined chicken bones led to a significant increase in the mobility of As when compared with the control soil. These findings illustrate that calcined eggshell in particular is equally effective as pure chemical additives in stabilizing Cd and Pb in a contaminated agricultural soil. The presence of As in metal-contaminated soils should be taken into consideration when applying phosphate-containing materials as soil additives, because phosphate can compete with arsenate on adsorption sites and result in As mobilization.  相似文献   

6.
Historical gold mining operations in Nova Scotia, Canada, resulted in numerous deposits of publicly accessible, arsenic (As)-rich mine waste that has weathered in situ for 75–150 years, resulting in a wide range of As-bearing secondary minerals. The geochemical heterogeneity of this mine waste creates a challenge for identifying a single remediation approach that will limit As mobility. A 30-cm-thick, low-organic content soil cover was evaluated in a laboratory leaching experiment where, to simulate natural conditions, the equivalent of 2 years of synthetic rainwater was leached through each column and two dry seasons were incorporated into the leaching protocol. Each column was a stratigraphic representation of the four major tailings types found at the historical Montague and Goldenville gold mine districts: hardpan tailings, oxic tailings, wetland tailings, and high Ca tailings. Hardpan tailings released acidic, As-rich waters (max 12 mg/L) under the soil cover but this acidity was buffered by surrounding oxic tailings. Leachate from the oxic tailings was circumneutral, with average As concentrations between 4.4 and 9.7 mg/L throughout the experiment. The presence of carbonates in the high Ca tailings resulted in near-neutral to weakly alkaline leachate pH values and average As concentrations between 2.1 and 6.1 mg/L. Oxidation of sulfides in the wetland tailings led to acidic leachate over time and a decrease in As concentrations to values that were generally less than 1 mg/L. This study shows that the use of a low-organic content soil cover does not create reducing conditions that would destabilize oxidized, As-bearing secondary phases in these tailings. However, oxygen penetration through the cover during dry seasons would continue to release As to tailings pore waters via sulfide oxidation reactions.  相似文献   

7.
Migmatites are widespread in the North Dabie ultrahigh-pressure metamorphic terrane (NDT) of Dabie orogen, East China. Idiomorphic and poikilitic amphibole grains in both leucosome and melanosome contain inclusions of plagioclase, quartz and biotite, suggesting formation of leucosome by fluid-present melting of biotite + plagioclase + quartz-bearing protoliths at P = 5–7 kbar, T = 700–800 °C. Precise SIMS zircon U–Pb dating indicates that migmatization of Dabie orogen initiated at ~140 Ma and lasted for ~10 Ma, coeval with the formation of low-Mg# adakitic intrusions in Dabie orogen. Based on mineralogical, petrographic and geochemical data, leucosomes in NDT can be subdivided into three groups. (1) High La/Yb(N)–Medium Sr/Y group (Group I), whose high Dy/Yb(N) but medium Sr/Y ratios are caused by amphibole and plagioclase residual during partial melting of dioritic to granodioritic gneisses. (2) Low La/Yb(N)–Low Sr/Y group (Group II), whose flat HREE patterns are produced by entrainment of peritectic amphiboles into melts derived from partial melting of dioritic gneiss. (3) High La/Yb(N)–High Sr/Y and Eu# group (Group III), whose extremely high Sr and Eu but low other REE concentrations are caused by accumulation of plagioclase and quartz. Although Group I and III fall in the adakitic fields on La/Yb(N)–Yb(N) and Sr/Y–Y diagrams, they are chemically distinct from contemporary high-pressure adakitic intrusions in Dabie orogen in a series of geochemical indexes, for example, lower Dy/Yb(N) and/or Sr/Y ratios at given La/Yb(N) ratio, lower Sr/CaO ratios, lower Rb concentration but higher K/Rb ratios. Therefore, leucosomes are produced by anatexis of the exhumed ultrahigh-pressure metamorphic rocks at middle crustal level, instead of partial melting of thickened lower crust with garnet-rich and plagioclase-poor residual. The coeval occurrence of migmatites and high-pressure adakitic intrusions in Dabie orogen indicates large-scale partial melting of middle to thickened lower crustal column in the early Cretaceous. The required heat source may be the mantle heat conducting through the lithospheric mantle whose lower parts have been convectively removed.  相似文献   

8.
Aluminum-containing hexagonally ordered mesoporous silica (Al-MCM-41) with specific surface area of 509.4 m2/g was first synthesized using natural halloysite as source material by hydrothermal treatment, without addition of silica or aluminum regents. The samples were characterized by X-ray diffraction, transmission electron microscopy, N2 adsorption–desorption measurements, and Fourier transform infrared spectra techniques. The results indicate that process parameters, including calcination temperature, pH value, n(SiO2)/n(CTAB)/n(H2O) ratio, and hydrothermal reaction time, show moderate effects on the preparation of Al-MCM-41. SiO2/Al2O3 molar ratio could be effectively modulated by the calcination temperature for halloysite. Furthermore, we first clarified the structural evolution from natural halloysite to mesoporous material Al-MCM-41 at the atomic level.  相似文献   

9.
Toxicity characteristic leaching procedure (TCLP) is a versatile short-term leaching protocol used to estimate the release of toxic metals from waste prior to disposal to a repository. This paper uses the integrated TCLP leachate data from tailings, tailings dam monitoring borehole data, and acidity ratio (AR) range of sulphide-rich ores to simulate the environmental TCLP As in tailings at the AngloGold Ashanti Obuasi mine in Ghana. The aim was to incorporate long-term leaching characteristics of tailings to minimise the risk of TCLP As test failure. The mean As concentration and pH value are 2.26 mg/l and 5.7 in TCLP leachate, 0.35 mg/l and 6.7 in monitoring boreholes, and?<?0.01 mg/l and 5.7 in control boreholes, respectively. The evaluation of the TCLP As data using a one-sample t test performed at 80% confidence interval has the upper confidence limit (UCL) of 2.41 mg/l; this value which constitutes the short-term characterised environmental TCLP As is below the USEPA criterion of 5 mg/l and, therefore, qualifies the waste as safe for disposal. Alternatively, TCLP leachate, borehole and AR data were integrated to simulate the long-term environmental TCLP As of 2.40 mg/l and pH value of 5.7, and As concentration and pH value of 0.01 mg/l and 6.7 in monitoring boreholes, respectively. Such laboratory simulations of TCLP As leaching aimed at achieving 0.01 mg/l in field monitoring data would provide a more robust predictive value for environmental management decision making due to long-term considerations.  相似文献   

10.
High fluoride and arsenic concentrations in groundwater have led to serious health problems to local inhabitants at Yuncheng basin, Northern China. In this study, groundwater with high fluoride and arsenic concentration at Yuncheng basin was investigated. A majority of the samples (over 60%) belong to HCO3 type water. The predominant water type for the shallow groundwater collected from southern and eastern mountain areas was Ca/Mg-Ca-HCO3 types. For the shallow groundwater from flow through and discharge area it is Na-HCO3/SO4-Cl/SO4/Cl type. The predominant water type for the intermediate and deep groundwater is of Na/Ca/Mg-Ca-HCO3 type. According to our field investigation, fluoride concentration in groundwater ranges between 0.31 and 14.2 mg/L, and arsenic concentration ranges between 0.243 and 153.7 μg/L. Out of seventy collected groundwater samples, there are 31 samples that exceed the World Health Organization (WHO) standard of 1.5 mg/L for fluoride, and 15 samples exceeds the WHO standard of 10 μg/L for arsenic. Over 40% of high fluoride and arsenic groundwater are related to the Na-HCO3 type water, and the other fifty percent associated with Na-SO4-Cl/HCO3-SO4-Cl type water; little relation was found in calcium bicarbonate type water. A moderate positive correlation between fluoride and arsenic with pH were found in this study. It is due to the pH-dependent adsorption characteristics of F and As onto the oxide surfaces in the sediments. The observed negative correlation between fluoride and calcium could stem from the dissolution equilibrium of fluorite. The high concentration of bicarbonate in groundwater can serve as a powerful competitor and lead to the enrichment of fluoride and arsenic in groundwater. Most of the groundwater with high fluoride or arsenic content has nitrate content about or over 10 mg/L which, together with the observed positive correlations between nitrate and fluoride/arsenic, are indicative of common source of manmade pollution and of prevailing condition of leaching in the study area.  相似文献   

11.
A laboratory investigation was carried out to examine the mechanism of arsenic (As) mobilization under flooded conditions (24 and 240 h) in 18 alluvial soils of Punjab, North–West India. Total dissolved As increased from a range of 3–16 μg L?1 (mean 9 μg L?1) to a range of 33–1,761 μg L?1 (mean 392 μg L?1) with the increase in flooding period from 24 to 240 h. The amount of As mobilization varied depending upon redox potential (pe) created by flooding conditions. After 24 h of flooded conditions, pe of soil water suspension ranged from ?1.75 to 0.77 (mean ?0.24). Increasing the flooding period to 240 h, pe of soil water suspension decreased in the range of ?4.49 to ?2.74 (mean ?3.29). Pourbaix diagram identified arsenate (HAsO4 2?) as predominant species in most of the alluvial soil–water suspensions under oxidized conditions, after 24 h of equilibration period, which ultimately transformed to arsenite (H3AsO3 0) after 240 h of anaerobic condition due to more reduced status. The solid phase identified was orpiment (As2S3). Identification of iron and manganese species in alluvial soil water suspension by Pourbaix diagram indicated decline in both soluble Fe2+ and SO4 2? concentration due to the formation of iron sulfide mineral phase after 240 h under anaerobic conditions. In these soils, decline in soluble Fe was also due to the precipitation of vivianite [Fe3(PO4)2·8H2O]. Elevated arsenic content and low pe value were measured in aquifers located in paddy growing fields comparative to aquifers of other sites. Large degree of variability in As concentrations was recorded in aquifers located at same sites. Thus, it is better to analyze each aquifer for their As content rather than to depends on the prediction on As content of neighbouring wells. The present investigation elucidates that flood irrigation practices in Punjab for growing paddy crop could induce the geochemical conditions favorable to mobilize arsenic from surface soils which could eventually elevate its content in the underlying shallow aquifers. Water abstracted from these aquifers by hand pumps or tube wells for drinking purposes could create hazards for local population due to loading with arsenic concentration above the safe limits. Thus, to avoid further contamination of shallow aquifers with arsenic, it is advisable to shift the flooded rice cultivation to other upland crops having lesser water requirement.  相似文献   

12.
New technologies such as microwaves have gained a large deal of attention from scientists and industries who sought increased rate of production processes. In this study, microwave irradiation was utilized to produce a novel KOH/Ca12Al14O33 nanocatalyst used for biodiesel production. As support, calcium aluminate was prepared by microwave combustion method using different fuels including urea, glycine, sorbitol, and citric acid. The samples were then impregnated by KOH to improve their catalytic activities for microwave-enhanced transesterification of canola oil for biodiesel production. Results of XRD, BET, FTIR, TG, EDX, and FE-SEM analyses showed differences in physicochemical properties of the samples when using different fuels with different flame characteristics and combustion temperatures. Only the urea-fueled sample showed the crystalline structure of monocalcium aluminate (CaAl2O4), with the other samples exhibiting amorphous structure of CaO–Al2O3. However, all samples, except for that prepared by citric acid, transformed to crystalline structure of Ca12Al14O33 by calcination during KOH impregnation. Among the samples, the KOH/Ca12Al14O33 nanocatalyst prepared by sorbitol showed the highest activity in microwave-enhanced biodiesel production because of its large surface area, pore size, and basicity, converting 93.4% of canola oil to biodiesel at a methanol-to-oil molar ratio of 18, catalyst concentration of 4 wt%, and microwave output power of 450 W in 60 min of reaction time. Moreover, the sample showed well-distributed particle sizes without any agglomeration, so that it could easily maintain its level of activity for several rounds of use.  相似文献   

13.
The first combined mineralogical and geochemical investigation of coal ashes from the Northwest Thrace Coal Basin, Turkey, was performed as a case study. The coal ash samples were obtained at 525 °C (group I), 750 °C (group II), and 1000 °C (group III) ashing temperatures from coal samples from the basin and were studied in terms of their mineralogical and geochemical composition using XRD and ICP-MS methods. The determination of the mineralogical composition was done for all of the groups; the geochemical analysis was carried out only for group II. In accordance with the high SiO2, Fe2O3, CaO, and SO3 content of the ash, quartz (SiO2), hematite (Fe2O3), and anhydrite (CaSO4) are the major crystalline phases for all of the ash groups. The other minerals are muscovite, thenardite, tridymite, calcite, wollastonite, anorthite, cristobalite, gibbsite, ternesite, mullite, nahcolite, and nacrite. High-temperature phases such as mullite, wollastonite, and anorthite were observed at 750 and 1000 °C. According to the (Fe2O3 + CaO + MgO+ K2O+ Na2O)/(SiO2 + Al2O3+ TiO2) ratios varying from 0.19 to 5.65, the ashes are highly prone to slagging. Compared to average values of low-rank coal ashes, the contents of V, Cr, Co, Ni, Zn, As, Rb, Sr, Mo, Cs, W, and U of the ash are higher, whereas the total content of rare earth elements (REEs) (Σ 163.7 ppm) are lower. Based on upper continental crust normalization, As, Se, Th, and U are enriched in all of the samples. The higher trace element contents in the ashes might be considered as a possible health hazard. The correlation analyses indicated that Ca is associated with anhydrite and As with hematite. The correlation analyses also showed that newly formed Al and Ca silicates may contain the elements such as Ti, K, Na, Cr, Sn, and Pb.  相似文献   

14.
Shao  Tongbin  Xia  Ying  Ding  Xing  Cai  Yongfeng  Song  Maoshuang 《中国地球化学学报》2020,39(3):387-403

Zircon stability in silicate melts—which can be quantitatively constrained by laboratory measurements of zircon saturation—is important for understanding the evolution of magma. Although the original zircon saturation model proposed by Watson and Harrison (Earth Planet Sci Lett 64(2):295–304, 1983) is widely cited and has been updated recently, the three main models currently in use may generate large uncertainties due to extrapolation beyond their respective calibrated ranges. This paper reviews and updates zircon saturation models developed with temperature and compositional parameters. All available data on zircon saturation ranging in composition from mafic to silicic (and/or peralkaline to peraluminous) at temperatures from 750 to 1400 °C were collected to develop two refined models (1 and 2) that may be applied to the wider range of compositions. Model 1 is given by lnCZr(melt) = (14.297 ± 0.308) + (0.964 ± 0.066)·M − (11113 ± 374)/T, and model 2 given by lnCZr(melt) = (18.99 ± 0.423) − (1.069 ± 0.102)·lnG − (12288 ± 593)/T, where CZr(melt) is the Zr concentration of the melt in ppm and parameters M [= (Na + K + 2Ca)/(Al·Si)] (cation ratios) and G [= (3·Al2O3 + SiO2)/(Na2O + K2O + CaO + MgO + FeO)] (molar proportions) represent the melt composition. The errors are at one sigma, and T is the temperature in Kelvin. Before applying these models to natural rocks, it is necessary to ensure that the zircon used to date is crystallized from the host magmatic rock. Assessment of the application of both new and old models to natural rocks suggests that model 1 may be the best for magmatic temperature estimates of metaluminous to peraluminous rocks and that model 2 may be the best for estimating magmatic temperatures of alkaline to peralkaline rocks.

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15.
Core sediments from three disturbed boreholes (JOR, GHAT, and RAJ) and two undisturbed boreholes (DW1 and DW2) were collected in the study area of the Chapai-Nawabganj district of northwestern Bangladesh for geochemical analyses. In the study area, groundwater samples from fourteen As-contained private wells and five nested piezometers at both the DW1 and DW2 boreholes were also collected and analyzed. The groundwater arsenic concentrations in the uppermost aquifer (10–40 m of depth) range from 3 to 315 μg/L (mean 47.73 ± 73.41 μg/L), while the arsenic content in sediments range from 2 to 14 mg/kg (mean 4.36 ± 3.34 mg/kg). An environmental scanning electron microscope (ESEM) with an energy dispersive X-ray spectrometer was used to investigate the presence of major and trace elements in the sediments. Groundwaters in the study area are generally the Ca–HCO3 type with high concentrations of As, but low levels of Fe, Mn, NO3 ? and SO 4 ?2 . The concentrations of As, Fe, Mn decrease with depth in the groundwater, showing vertical geochemical variations in the study area. Statistical analysis clearly shows that As is closely associated with Fe and Mn in the sediments of the JOR core (r = 0.87, p < 0.05 for Fe and r = 0.78, p < 0.05 for Mn) and GHAT core (r = 0.95, p < 0.05 for Fe and r = 0.93, p < 0.05 for Mn), while As is not correlated with Fe and Mn in groundwater. The comparatively low Fe and Mn concentrations in some groundwater and the ESEM image revealed that siderite precipitated as a secondary mineral on the surface of the sediment particles. The correlations along with results of sequential extraction experiments indicated that reductive dissolution of FeOOH and MnOOH represents a mechanism for releasing arsenic into the groundwater.  相似文献   

16.
《International Geology Review》2012,54(12):1490-1505
We studied a high-pressure amphibole-bearing migmatite cropping out along the northeastern coast of Sardinia, a few kilometres northeast of Olbia, in order to improve our knowledge about its evolution using pressure–temperature (P–T) pseudosections. Thermodynamic calculations with PERPLE_X were undertaken in the system Na2O–K2O–CaO–FeO–MnO–MgO–Al2O3–TiO2–SiO2–H2O using a haplogranitic melt model. Calculations were conducted for average compositions of the protolith and the tonalitic leucosome with different contents of H2O to construct various pseudosections in the P–T range 2–20 kbar and 550–900°C. We demonstrate that the molar ratios Na/K and Si/Al of the anatectic melt are of high geothermobarometric value. Particularly the melt field in the P–T pseudosection for the protolith, contoured by Si/Al isolines, shows a significant decrease in this ratio with rising pressure. This ratio is only weakly dependent on variable H2O contents of the amphibole-bearing migmatite as demonstrated by contoured T–H2O pseudosections. The application of the Na/K and Si/Al ratios in melt yielded P–T conditions close to 13 kbar and 700°C, assigned as the conditions of partial melting. Evaluation of contoured P–T pseudosections for the leucosome composition resulted in conditions of about 10.5 kbar and 700°C for the crystallization of amphibole in the leucosome melt, and 9 kbar and 680°C for complete crystallization of this melt.  相似文献   

17.
Activated carbon is the adsorbent commonly used to remove arsenic from contaminated water. However, the problem is that it is not always available everywhere and considered expensive in developing countries. An inexpensive alternative to activated carbon can therefore aid the adequate treatment of contaminated water. Tea waste, water hyacinth and banana peel are investigated extensively in this study as the inexpensive alternative. Tea waste treated with a right proportion of aqueous FeCl3 reagent is found to have substantially higher arsenic removing capacity (which is quantified by arsenic concentrations measured employing Double Beam Atomic Absorption Spectrophotometer) than the other two. The comparison made subsequently between tea waste and activated carbon reveals the feasibility of the utilization of tea waste. The arsenic removing capacity of tea waste treated with the right proportion of aqueous FeCl3 reagent is found to be equal to that of the activated carbon treated with the same reagent over the continuous operative time of 2 h. The tea waste treated rightly with the same reagent also removes arsenic at acceptable capacities over extended operative times such as 4–6 h. It is therefore proposed to consider tea waste as the inexpensive alternative to activated carbon in treating arsenic contaminated water.  相似文献   

18.
《International Geology Review》2012,54(13):1666-1689
ABSTRACT

The Wulonggou area in the Eastern Kunlun Orogen (EKO) in Northwest China is characterized by extensive granitic magmatism, ductile faulting, and orogenic gold mineralizations. The Shidonggou granite is located in the central part of the Wulonggou area. This study investigated the major as well as trace-element compositions, zircon U–Pb dates, and zircon Hf isotopic compositions of the Shidonggou granite. Three Shidonggou granite samples yielded an average U–Pb zircon age of 416 Ma (Late Silurian). The Late Silurian Shidonggou granite is peraluminous, with high alkali contents, high Ga/Al ratios, high (K2O + Na2O)/CaO ratios, and high Fe2O3T/MgO ratios, suggesting an A-type granite. The Shidonggou granite samples have zircon εHf(t) values ranging from ?7.1 to +4.4. The Hf isotopic data suggest that the Late Silurian granite was derived from the partial melting of Palaeo- to Mesoproterozoic juvenile mantle-derived mafic lower crust. Detailed geochronological and geochemical data suggest that the Late Silurian granite was emplaced in a post-collisional environment following the closure of the Proto-Tethys Ocean. Combining data of other A-type granitic rocks with ages of Late Early Silurian to Middle Devonian, such post-collisional setting related to the Proto-Tethys Ocean commenced at least as early as ~430 Ma (Late Early Silurian), and sustained up to ~389 Ma (Middle Devonian) in the EKO.  相似文献   

19.
This study investigated the leaching of radium-226 from phosphogypsum (PG) waste produced from the fertilizer industry by synthetic solutions that replicate water that may contact the waste in natural conditions. The results indicated that the activity concentration of Ra-226 in the PG was 461 ± 12 Bq kg?1 and compared with other studies carried out worldwide. The leached percentage of Ra-226 represents the exchangeable fraction loosely bounded in the matrix of the PG waste. The leached fraction of Ra-226 was 6.5 ± 0.6 and 9.0 ± 0.5% when the waste was exposed to rainwater and saline solution, respectively. It is also found that the leaching fraction increased 10–12 ± 0.4% when the waste was exposed to the admixture of saline solution containing Sr2+ or Ba2+ cations, whereas it was lowered to 4–5 ± 0.5% in the presence of carbonate or sulfate anions. When the PG is used as an economic fertilizer, the irrigation water can leach 7.8 ± 0.6% of Ra-226 that could contribute to plant uptake, thereby to animal and/or human consumption. The primary tests of the drinking water (well and tap resources) consumed by the populations surround the PG facility showed that the activity concentration of Ra-226 was below the minimum detectable activity.  相似文献   

20.
An industrial area contaminated by As was studied to determine the source of this element and its speciation in As-bearing solids and in run-off waters. Mineral precipitates and water samples were collected and analyzed to assess processes controlling As mobility at this site. The integrated study of a contaminated industrial area allowed identification of the source of the As and of the nature of secondary As-bearing phases. The results obtained both on solid and water samples were used to model As behavior during waste leaching on carbonate rocks. At the upper end of a topographic transect across the site, run-off waters (pH=7.9) interact with surficial waste piles (containing arsenolite, arsenopyrite and pyrite), becoming acidic (pH=2.2) and concentrated in dissolved arsenate species (As5+) (ΣAs ranging from 0.961 to 3.149·10−3 mol/l). Those acidic waters interact with the limestone substratum, providing dissolved Ca which reacts with As to precipitate 1:1 Ca arsenates (weilite CaHAsO4, haidingerite CaHAsO4.H2O and pharmacolite CaHAsO4.2H2O) and, in minor amounts, Ca–Mg arsenates (picropharmacolite (Ca,Mg)3(AsO4)2 6H2O). The 1:1 Ca arsenates identified are known to precipitate at low pH (3–6) and seem to be stable in media with high dissolved CO2, in comparison with other types of Ca arsenates. However, due to their high solubilities, they are not strictly relevant candidates to immobilize As in contaminated surficial environments. Although reported solubilities decrease to values close to the French and US drinking standards in Ca-rich solutions, a thorough examination of the precipitation/dissolution kinetics of Ca arsenates should be undertaken to assess their long-term stability and their efficiency in rapidly immobilizing As in contaminated surficial environments.  相似文献   

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