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1.
The present paper undertakes a study of the physico-chemical properties and toxic heavy metals content in the untreated and treated pharmaceutical effluents in order to evaluate the working efficiency of industrial effluent treatment plants. The treatment efficiency achieved for various parameters was conductivity (79.94%), alkalinity (93.91%), hardness (87.70%), chloride (89.24%), cyanide (79.66%), phosphate (99.19%), total dissolved solids (85.89%), total suspended solids (96.87%), salinity (52.41%), dissolved oxygen (27.32%), biochemical oxygen demand (83.39%) and chemical oxygen demand (72.21%). The removal efficiency achieved for different heavy metals was Cu2+ (79.66%), Ni2+ (69.22%), Cr6+ (80.15%), Pb2+ (72.14%), Fe3+ (92.59%) and Zn2+ (90.61%). The level of biochemical oxygen demand (64 mg L?1) in the treated effluents was above the limit of 30.0 mg L?1, chemical oxygen demand level (208 mg L?1) was close to a limit of 250 mg L?1, while average Pb2+ concentration (0.10 mg L?1) was on the borderline of maximum permissible limit of 0.10 mg L?1 set by Central Pollution Control Board for safe discharge of industrial effluent in inland surface water. The average concentration of cyanide (0.01 mg L?1) in the treated industrial effluent of our study is of great concern to the fisheries of freshwater ecosystem in which the effluents finally get discharged. Based on the results of the present study, it is concluded that the pollution level in the discharged pharmaceutical effluent is of the great concern requiring proper treatment and regular scientific monitoring so as to protect the environmental degradation of water resources and facilitate the propagation of the aquatic life.  相似文献   

2.
Aluminium smelters are major sources of F emission to the environment. We studied, in laboratory experiments, the sorption and desorption of fluoride on organic and mineral horizons of soils located within 2 km from one of these factories, situated in the northern coast of Galicia (NW Spain). The soils, developed from granite, are acid (pH H2O 3.9–5.5), rich in organic matter (4–16 % C in the A horizon) and most A horizons have high Al saturation in the exchange complex. All samples showed a notable F sorption, between 1,066 and 1,589 mg kg?1, after adding 200 mg F L?1, which accounts for 53–80 % of F added. The sorption was slightly higher in the A horizons than in the respective organic horizons (differences of up to 194 mg kg?1). The fluoride sorption upon addition of 200 mg F L?1 correlated significantly (p < 0.05) with soil pH in water (r = ?0.77), iron extracted by acid ammonium oxalate (r = 0.68), aluminium plus iron extracted by acid ammonium oxalate (r = 0.63), exchange aluminium (r = 0.52) and clay percentage in soil (r = 0.76). The F sorption fitted to both Langmuir and Freundlich models. Desorbed F accounted for only 12–22 % of sorbed fluoride and correlated (p < 0.05) negatively with non-crystalline (extracted by acid ammonium oxalate) Fe (r = ?0.51) and clay content (r = ?0.74) and positively with organic matter (r = 0.69) and with the effective cation exchange capacity of the soil (r = 0.50).  相似文献   

3.
A simple spectrophotometric method for determination of hydrogen sulfide in wastewater and hot spring samples was developed. The method is based on the reaction between hydrogen sulfide and sodium 1,2-naphthoquinone-4-sulfonate (NQS). The effect of various experimental factors on the reaction between hydrogen sulfide and NQS was investigated and optimized using central composite design. The optimal values of the factors were 5.00 × 10?4 mol L?1 for concentration of NQS and 1.00 × 10?2 mol L?1 for concentration of hydrochloric acid. The wavelength of the maximum absorption of the reaction product was 320 nm. Constructed calibration curve for hydrogen sulfide determination was linear in the range of 0.5–20.0 mg L?1 with the detection limit of 0.16 mg L?1. The method was free from interferences. Percent relative errors below 2 % were obtained for determination of hydrogen sulfide in environmental samples.  相似文献   

4.
An electrochemical advanced oxidation process employing a boron-doped diamond anode for the treatment of synthetic waters and secondary effluents of wastewater treatment plants (WWTP) was studied. The efficiency and formation of transformation products (TPs) for this treatment process were investigated at different current densities for bisphenol A (BPA) spiked to synthetic water and WWTP effluents. A complete removal of the parent compound was achieved in WWTP effluents. Higher applied current densities resulted in faster removal. At the same time, a correlation between the applied current density and the ozone concentration measured in the bulk solution was revealed. Hence, the observed transformation of BPA is likely due to the generation of reactive oxygen species such as hydroxyl radicals and ozone. Based on a suspected target screening approach, four known TPs and two unreported (new) TPs were identified by LC–MS analysis. These results suggest a transformation pathway following three steps: hydroxylation of the aromatic ring, followed by oxidation of the isopropylidene bridge and finally a ring opening and formation of organic acids and other small molecules. The presence of chloride ions in WWTP effluents can result in the generation of excessive concentrations of chlorate and perchlorate during electrochemical oxidation. Applying a current density of 208 mA cm?2, a complete elimination of BPA was achievable after 15 min (Q/V = 430 mA h L?1); however, the oxidation resulted in concentrations of chlorate and perchlorate of 2.85 and 5.65 mg L?1, respectively. These values were directly dependent on the exposure time and desired degree of BPA removal.  相似文献   

5.
The role of organic ligands in metal complexing in natural waters has received little attention because of uncertainties regarding both the abundance and nature of dissolved organic carbon compounds. Recent data show that the bulk of dissolved organic matter in natural waters consists of highly oxidized and chemically and biologically stable polymeric compounds closely resembling soil humic substances. Average molar concentrations of these aquatic humics in major U.S. rivers range from 5 × 10?6to 3 × 10?5 moles 1?1. Fractional elution of soil organic matter by meteoric waters may be considered to be the main process contributing to the presence of humic matter in rivers. The aquatic humic polymers participate in complex formation through ionizable functional groups with a range of differential acidities. The stabilities of metal-humic complexes in natural waters are higher than those of the corresponding inorganic metal complexes. Quantitative evaluation of the metal-organic interactions can be approached by applying variable equilibrium functions which take into account the differential physico-chemical characteristics of the active complexing sites on the polymer molecule. Assuming an average humic concentration of 10 mg 1?1, complexation of trace metals can be significant even in the presence of excess concentrations of major cations.  相似文献   

6.
El Bey river, which drains 60% of the pollutant load of several urban cities in the northeast of Tunisia, provides a good example of the transfer of organic and metallic pollutants that result from industrial and urban activity, and can be used to show how these charges are transported and discharged into the Gulf of Tunis. Persistent organic pollutants (PAH and PCB) in dissolved, particulate matter, bed sediments, and three wastewater effluents in El Bey watershed were analyzed. PAH (∑14PAHs) concentration ranged from 0.248 to 9.955 mg L?1 and from 0.836 to 28.539 mg L?1 in dissolved and particulate fraction respectively. The particulate/dissolved partition coefficient value (Kd) was less than one which confirmed the affinity of PAH to be adsorbed. In sediment, the high-molecular weight PAHs were found principally with percentage between 50 and 100% witch present 239.99 to 5362.19 μg kg?1, which is relatively higher in comparison with other estuaries river. Contrary to PAH patterns, PCB were bound to dissolve fraction. Kd (PCB) value (Kd?>?1) reflected this affinity which is related to environment energy. The spatial distribution and profile of analyzed organic pollutants confirmed the direct impact of wastewater effluent on the organic pollution level in three compartment of El Bey watershed and his profiles suggested different transport patterns.  相似文献   

7.
The main objective of this study is to investigate the possibility of powdered eggshell used as an adsorbent material for removal of humic acid from peat water. The influences of contact time, dose of eggshells, pH, and temperature were the factors considered in the removal processes of humic acid from peat water. In addition, adsorption isotherms of humic acid onto the powdered eggshell were also evaluated with the Langmuir and Freundlich approximations. Our results showed that the equilibrium of the process was eventually established after 60 min of the contact time, and also found that using 5 g of the powdered eggshell nearly 95 % of humic acid has been successfully removed from the peat water. The removal of humic acid gave better result when it was conducted at low pH, and it was almost unaffected the temperatures variation. The data was well fitted to Freundlich isotherm with the correlation coefficient of not <0.999, and could uptake the humic acid about 126.58 mg/g at pH 4.01, estimated from the Langmuir model. The kinetic experimental data proportionally correlated with the pseudo-second-order kinetic model with a rate constant in the range of 0.016–0.112 g mg?1 min?1, while intra-particle-diffusion were the main rate determining step in the humic acid removal process. The powdered eggshell investigated in this study, thus, exhibited as a high potential adsorbent for the removal of humic acid from peat water.  相似文献   

8.
Recently, microalgae are considered as lipid sources for biodiesel production. A photobioreactor was designed and fabricated for Scenedesmus sp. microalgae cultivation. The effect of several nitrogen sources, light intensity, iron ions, silicon, magnesium sulfate and ethanol concentrations on Scenedesmus sp. microalgae growth were investigated. For incubation period of 8 days, sodium nitrate and ammonium carbonate were the best nitrogen sources with biomass concentrations of 2.373 and 2.254 g L?1, respectively. Microalgae growth was reduced using nitrogen concentrations above 0.7 g L?1. In the first 10 days of incubation, maximum cell dry weight (0.7 g L?1) was obtained with light intensity of 10,000 lx, whiles after that, the results were desired (1 g L?1) using interior lighting at 7500 lx. Magnesium sulfate had a positive effect on cell growth. The biomass concentration of 1.65 g L?1 was obtained using 0.06 g L?1 magnesium sulfate. Maximum obtained biomass with silicon (0.7 Mm), ethanol (1.8 mL L?1) and ferric ammonium citrate (0.02 g L?1) was 1.7 and 1.3 and 2.16 g L?1, respectively. Logistic model was found to be a suitable model for cell growth forecast. Fatty acid analysis showed that composition of the most dominant synthesized fatty acids, palmitic and oleic acids, was 21.16 and 33.58%, respectively. Oil produced by Scenedesmus sp. microalgae composed of 49.08% saturated and 43.53% unsaturated fatty acids has a suitable composition for a desired biodiesel.  相似文献   

9.
Lead (Pb) dust exposure can have detrimental environmental and human health effects. Improperly enclosed stockpiles of Pb concentrates can cause dust emissions, subsequent pollution of the soil and environmental risk. The aim of this work was to study Pb form, distribution and immobilization (by using eggshell and seashell) in an industrial arid soil near a storage area of Pb mineral concentrates in northern Chile. High amounts of sulfur (S; 9900 mg kg?1) and Pb (6530 mg kg?1) were found in the polluted soil. The energy-dispersive X-ray spectroscopy analysis revealed a lead sulfide (PbS: galena). Metallic Pb particles, which were between 41 and 46 µm, were identified in the soil. After eggshell and seashell (20%) were applied, the soil pH increased from 6.0 to 7.84 and 8.07, respectively. In the studied soil, the leaching test showed a 59 mg L?1 average Pb extractable concentration. After 240 days, extractable Pb by toxicity characteristics leaching procedure decreased to 4.79 mg L?1 (93.3%) with the application of seashell at 20% compared with a decrease of 33.33 mg L?1 (53.6%) using eggshell. Pb in the polluted soil was mainly found in the exchangeable fraction (66%), followed by the reducible (24%), residual (7%) and oxidizable (6%) fractions. According to the risk assessment code, the contaminated soil before treatment was classified as very high risk. Adding eggshell (20%) and seashell (20%) decreased the exchangeable fractions to 39 and 35%, respectively. Applying these liming materials achieved Pb immobilization in the soil, but the soil remained in the high environmental risk category. We conclude that the application of seashell waste, resulting from high aquaculture activity, opens an interesting window to the treatment of contaminated arid soils.  相似文献   

10.
Irrigation by treated wastewater (TWW) can pollute the soil by different organic and inorganic compounds. The pollution level can depend on the irrigation period, soil nature, and wastewater characteristics. Since 1989, the Zaouit Sousse area (central Tunisian) has been irrigated by treated wastewater. The irrigation period and the mineralogy of soil composition change from one locality to another in Zaouit Sousse area. In this work, we are interested in organic compounds, polycyclic aromatic hydrocarbons (PAHs), and heavy metals (HMs) evolution. One control soil (S1) and four irrigated areas soil (S2, S3, S4, and S5) were chosen. The soil samples differ by the irrigation period and soil characteristics. Total PAHs content in control soil was 66.2 ng?g?1 and in irrigated areas were between 46.23 and 129.51 ng?g?1. The PAHs content in irrigated soil, except S5 which has been irrigated with wastewater for 20 years and contains the highest clay fraction percent, decreased with the irrigation period (from 0 to 20 years). The microbial degradation may decrease the PAHs concentrations in the soil thanks to bacterium brought by TWW and the important soil permeability. Concentration of heavy metals ranged from 24 to 1,320 μg?L?1. The HMs (Cu, Cr, Zn, Fe, Ni, Pb, and Cd) contents decreased with the irrigation period (from 10 to 20 years). So, following the PAHs aerobic bio-degradation, this organic compound discharges their absorbed heavy metals which leached to deeper levels. The Cr, Cu, Al, Zn, and Cd mobility depend on the clay yield too. However, the PAHs and Pb mobility are also related to humic substance quantities. Cr and Cu have affinities both to clay and humic substance quantities.  相似文献   

11.
Underground contamination water by herbicides depends on the interactions between their molecules with physical and chemical soil characteristics and climatic conditions. Studies with columns can estimate the leaching potential of herbicides in soils. This study aimed to determine the effect of soil pH on tebuthiuron leaching, and capacity of bioindicators to detect tebuthiuron residues in three Brazilian soils. Cucumber plants (Cucumis sativus) were more negatively affected when grown in soils with lower amounts of organic matter and clay, and in these soils, the tebuthiuron levels reached greater depths in the column. There was a positive correlation between tebuthiuron concentration and cucumber intoxication, and a negative correlation between tebuthiuron concentration and dry matter cucumber in all soils. The tebuthiuron leached up to 50 cm depth even in soils with higher organic matter and clay content. The increasing of soil pH can affect the leaching of nonionic herbicides, and liming practice may elevate the environmental contamination risk by tebuthiuron. The bioindicator method using Cucumis sativus is viable and can be recommended to detect tebuthiuron concentrations above 0.2 mg kg?1.  相似文献   

12.
Understanding the effects of organic acids (OA) on the transformation of Fe and Mn to surface water from the weathering coal gangue is of great benefit to risk assessment and remediation strategies for contaminated water and soil. Based on the investigation on surface water in the central coal districts of the Guizhou Province, 18 water samples were collected for heavy metal analysis. The results indicated that the pH value of surface water is low (3.11–4.92), and Fe concentration (1.31–5.55 mg L?1) and Mn concentration (1.90–5.71 mg L?1) were, on average, 10.86 and 34.33 times the limit of Surface Water Quality Standards, respectively. In order to evaluate the effects of the OA on the dissolution of Fe and Mn from the weathering coal gangue, column elution and batch leaching experiments were conducted. The results show that the low molecular weight of organic acids (LMWOAs, i.e., oxalic, tartaric, malic and citric acids) and fulvic acids significantly accelerated the dissolution of Fe and Mn; in addition, when the concentration of OA reached 25 mmol L?1, the concentrations of Fe, and Mn were 1.14–67.08 and 1.11–2.32 times as high as those in 0.5 mmol L?1 OA, respectively. Furthermore, the migration of Fe and Mn was significantly influenced by the pH and Eh, especially for Fe; the ion Mn was dissolved from the gangue more easily than the ion Fe in the column leaching, which was contrary to the results of batch leaching.  相似文献   

13.
Soil salinity and sodicity are escalating problems worldwide, especially in arid and semiarid regions. A laboratory experiment was conducted using soil column to investigate leaching of soluble cations during reclamation process of a calcareous saline–sodic soil (CaCO3?=?20.7%, electrical conductivity (EC)?=?19.8 dS m?1, sodium absorption ratio (SAR)?=?32.2[meq L?1]0.5). The amendments consisted of control, cattle manure (50 g kg?1), pistachio residue (50 g kg?1), gypsum (5.2 g kg?1; equivalent of gypsum requirement), manure + gypsum and pistachio residue + gypsum, in three replicates which were mixed thoroughly with the soil, while sulfuric acid as an amendment was added to irrigation water. To reflect natural conditions, after incubation period, an intermittent irrigation method was employed every 30 days. The results showed that EC, SAR, and soluble cations of leachate for the first irrigation step were significantly higher than those of the subsequent leaching runs. Moreover, the concentration of removed soluble cations was lower for the control and gypsum-treated soils. It was found that among applied amendments, treatments containing cattle manure showed higher concentrations of sodium, calcium, and magnesium in the leachate, while due to pistachio residue application, further amount of potassium was removed out of soil column. The addition of pistachio residue resulted in the highest reduction in soil salinity and sodicity since the final EC and exchangeable sodium percentage dropped to 18.0% and 11.6% of their respective initial values, respectively. In the calcareous soil, solubility of gypsum found to be limited, in contrast, when it was added in conjunction with organic amendments, greater amounts of sodium were leached.  相似文献   

14.
In the present study, a widely used reactive dye, Color Index (C.I.) Reactive Blue 268 was utilized for mycoremediation by Aspergillus fumigatus isolated from textile effluent. Complete decolorization of the test dye (0.1 g L?1) was recorded within 6 days of static incubation at 27 °C in Czapek Dox broth (CDB). However, the isolate was unable to utilize the dye as a sole source of energy in Czapek Dox agar and CDB in absence of sucrose and obligate requirement of a labile carbon source, i.e., sucrose needed for induction of decolorization. Biosorption seems to play the pivotal role in decolorization as evident by coloring of the fungal biomass as that of dye color. The optimal conditions for the highest decolorization were found at 30 °C and pH 6.0 with 6-day-old inoculums supplemented with sucrose (10 g L?1) and ammonium chloride (2 g L?1) as a carbon and nitrogen source, respectively. The response of the isolate to increasing dye concentrations was found to be growth inhibitory. Surprisingly, about 65 % of dye decolorization was recorded with heat-inactivated biomass powder within 6 days of static incubation supporting the fact of fungal biosorption. Results of this study have established the candidature of the isolate for biotechnological removal of dyes from disreputable dying effluents.  相似文献   

15.
Eutrophication is considered the most important water quality problem in freshwaters and coastal waters worldwide promoting frequent occurrence of blooms of potentially toxic cyanobacteria. Removal of cyanobacteria from the water column using a combination of coagulant and ballast is a promising technique for mitigation and an alternative to the use of algaecides. In laboratory, we tested experimentally the efficiency of two coagulants, polyaluminium chloride (PAC) and chitosan (made of shrimp shells), alone and combined with two ballasts: red soil (RS) and the own lagoon sediment, to remove natural populations of cyanobacteria, from an urban brackish coastal lagoon. PAC was a very effective coagulant when applied at low doses (≤8 mg Al L?1) and settled the cyanobacteria, while at high doses (≥16 mg Al L?1) large flocks aggregated in the top of test tubes. In contrast, chitosan was not able to form flocks, even in high doses (>16 mg L?1) and did not efficiently settle down cyanobacteria when combined with ballast. The RS itself removed 33–47 % of the cyanobacteria. This removal was strongly enhanced when combined with PAC in a dose-dependent matter; 8 mg Al L?1 was considered the best dose to be applied. The lagoon sediment alone did not promote any settling of cyanobacteria but removal was high when combined with PAC. Combined coagulant and ballast seems a very efficient, cheap, fast and safe curative measure to lessen the harmful cyanobacteria bloom nuisance in periods when particularly needed, such as around the 2016 Olympics in Jacarepaguá Lagoon.  相似文献   

16.
Greenhouse tests were conducted to study the effect of chelates on the phytoextraction of cadmium and lead, and the rhizodegradation of used engine oil present as a mixed contaminant in a sandy soil. Indian mustard plants were grown in test pot soil for 30 days and chelates ethylenediamine tetraacetic acid (EDTA) and ethylenediaminedisuccinic acid (EDDS) were individually applied to the test soil. The soil was spiked earlier with 50 mg kg?1 of CdCl2, 500 mg kg?1 of PbCl2 and 500 mg kg?1 of used engine oil to form the mixed soil contaminant. At the same concentration of chelates, EDTA was found to be more effective than EDDS in increasing the concentration of metal contaminants Cd and Pb in the plant. Compared to EDDS, EDTA was also more effective in promoting rhizodegradation of the organic contaminant formed by used engine oil. The study demonstrated that the application of chelates to soils containing mixed contaminants such as heavy metals (Cd and Pb) and organics (used engine oil) can simultaneously assist metal accumulation at higher concentrations in the biomass of Indian mustard plant and also reduce the amount of used engine oil in the soil through rhizodegradation.  相似文献   

17.
The potential of the autoclaved Tunisian landfill leachate treatment using microalgae (Chlorella sp.) cultivation was investigated in this study. Landfill leachate was collected from Borj Chakir landfill, Tunisia. A full factorial experimental design 22 was proposed to study the effects of the incubation time and leachate ratio factors on the organic matter removal expressed in chemical oxygen demand (COD) and ammoniacal nitrogen (NH4─N) and on the biological response of Chlorella sp. expressed by the cell density and chlorophyll content. All experiments were batch runs at ambient temperature (25 ± 2 °C). The Chlorella sp. biomass and chlorophyll a concentrations of 1.2 and 5.32 mg L?1, respectively, were obtained with 10% leachate spike ratio. The obtained results showed that up to 90% of the ammoniacal nitrogen in landfill leachate was removed in 10% leachate ratio spiked medium with a residual concentration of 40 mg L?1. The maximum COD removal rate reached 60% within 13 days of incubation time indicating that microalgae consortium was quite effective for treating landfill leachate organic contaminants. Furthermore, with the 10% leachate ratio spiked medium, the maximum lipid productivity was 4.74 mg L?1 d?1. The present study provides valuable information for potential adaptation of microalgae culture and its contribution for the treatment of Tunisian landfill leachate.  相似文献   

18.
The effects of inactivation agents, including common polymeric aluminium (Al) chloride (CPAC) and Ecological Type PAC (UNIC), on phosphorus (P) released from sediment are unclear. To determine these effects, we performed seven experiments using various inactivation agent additions. The experimental schemes used were as follows: (1) CPAC, 15 mg Al L?1; (2) CPAC (15 mg Al L?1) + polyacrylamide (PAM) (0.5 mg L?1); (3) UNIC, 5 mg Al L?1; (4) UNIC, 15 mg Al L?1; (5) UNIC, 60 mg Al L?1; (6) control set without any inactivation agent addition; and (7) alkali shock load (the pH value of overlying water in the scheme 7 was adjusted to 11 by addition of sodium hydroxide to simulate alkali shock load at 13 days after CPAC addition). The experiments were conducted in glass columns, each containing 0.3 L sediment from Lake Dianchi and 3 L of overlying water. The results showed that P release rate decreased as the amount of inactivation agent added increased. P release rate was calculated according to each inactivation agent and the amount of inactivation agent added. Release rate found was in the decreasing order: (6) > (3) > (4) > (1) > (5) > (2). The corresponding rate was calculated to be 7.11, 6.16, 4.55, 1.76, 1.46 and 1.00 mg P m?2 day?1, respectively. Dissolved total P (DTP) was the main form of total P (TP) in the overlying water. After the addition of PAM, the DTP:TP ratio decreased while the dissolved inorganic P (DIP):DTP ratio increased. With increasing the amount of inactivation agents added, both DTP:TP and DIP:TP ratios decreased. Experimental group 3 had similar DTP:TP and DIP:TP ratios to experimental group 6. These results are significant in terms of the large-scale application of inactivation agents for reducing levels of bioreactive P. Alkali shock load (experimental group 7) caused failure in the inactivation of P by CPAC.  相似文献   

19.
The mechanism for reclaiming sodic soils using calcium sulfate (CaSO4) could provide a theoretical basis for the field application of CaSO4 substitutes, including the by-products of flue gas desulfurization (BFGD), fly ash, and phosphorus gypsum. In this study, Ca2+ application experiment was conducted to analyze the dynamic changes of the cations in the reclamation of sodic soils with CaSO4. A multicomponent solute transport model (UNSATCHEM) that considers ion adsorption exchange and dynamic changes in the soil’s hydraulic conductivity was subsequently used to simulate and predict the movement of ions. The Ca2+ application experiment consisted of four treatments with four CaSO4 concentrations (0.5, 1, 1.5, and 2 g L?1). When the Ca2+ concentrations in the supplied water were 14.71, 22.06, and 29.41 mmol L?1, Ca2+ achieved penetration, and this process was faster when the Ca2+ concentration in the supplied water was higher. Ca2+ did not achieve penetration when the Ca2+ concentration was 7.35 mmol L?1. UNSATCHEM was able to simulate the transportation mechanism of Ca2+ and Na+ in the soil solution in the Ca2+ application experiment, the adsorption and exchange between the Na+ in the soil colloid and Ca2+ in the soil solution, and the precipitation and dissolution of CaSO4 with a high degree of accuracy. Sodic soil reclamation with CaSO4 was not a short-term process. Compared with applying CaSO4 only once, applying CaSO4 in batches decreased the accumulation of soil salts and promoted its dissolution.  相似文献   

20.
Colloidal pyrite waste rocks (CPWR) which are mainly composed of colloidal pyrite and siderite widely deposit in sulfide mines in the middle and lower reaches of the Yangtze River belt, China, especially in Tongling City, Anhui Province, China. In this paper, a fixed-bed column was used to investigate the weathering and oxidation of CPWR and its role in immobilizing low-concentration Cu (10 mg L?1) under weakly acidic leach (pH = 5.0). The experimental results indicated that the breakthrough capacity was around 14.0 mg Cu g?1 CPWR when Cu2+ breakthrough concentration was 0.5 mg L?1. Sequential extraction of Cu and dithionite–citrate–bicarbonate extraction of free iron in the used CPWR after the column breakthrough indicated that Cu removal by CPWR consisted of the following processes: oxidation of pyrite and dissolution of siderite in CPWR, ferrous oxidation, and adsorption of Cu on ferric (hydr)oxides. This study shows the potential application of CPWR as an effective sorbent for the removal of low-concentration Cu from acid mine drainage.  相似文献   

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