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1.
Adsorption of copper and zinc by oil shale   总被引：8，自引：0，他引：8  
 Oil shale is able to remove appreciable amounts of copper and zinc ions from aqueous solutions. It was noted that an increase in the adsorbent concentration with constant copper or zinc concentration resulted in greater metal removal from solution. An increase in the copper or zinc concentration with a constant sorbent concentration resulted in higher metal loading per unit weight of sorbent. For both metals, copper and zinc, equilibrium was attained after 24-h contact time. Increase in the initial pH or temperature of the metal solution resulted in an increase in the metal uptake per unit weight of the sorbent. Freundlich isotherm model was found to be applicable for the experimental data of Cu2+ and Zn2+. The results showed that oil shale could be used for the adsorption of the Cu2+ and Zn2+ with higher affinity toward Zn2+ ions. Addition of sodium salt to the metal solution influenced copper removal positively, but inhibited zinc removal. Received: 3 January 2000 · Accepted: 27 June 2000  相似文献   

2.
The problem associated with multi-metals contaminated soils has generated increasingly more attention. Thus, it is necessary within the field to study the mutual influence of environmental factors on competitive adsorption. The majority of studies carried out to date have concentrated on the variation of adsorption capacity or the removal efficiency, with only a single factor changed (including pH, ionic strength, and metal concentration). However, the interaction effect among various environmental factors was ignored in these studies. The purpose of this study was mainly aimed toward the investigation of the interaction of two influential factors, as well as the influential degree of each factor (such as the initial pH, ionic strength, initial metal concentration, and the competitive metal concentration) on competitive adsorption using the response surface method. These results demonstrated that the influential degree of each factor studied on the competitive adsorption of Zn2+ and Cd2+ followed the trend of having the initial concentration of the target metal?>?initial pH?>?concentration of competitive metal?>?ionic strength. When the metal concentration was held constant, we found that the competitive adsorption of Zn2+ initially increased, followed by a decrease with increasing initial pH. However, this was found to change minimally with increasing ionic strength. When the initial pH or ionic strength was held constant, the competitive ability was observed to increase with increasing Zn2+ concentration. However, with increasing Zn2+ or Cd2+ concentrations, the variation degree of the competitive adsorption was found to become smaller. These results provide novel information toward a better understanding of the effect of multifactors on the competitive adsorption of Zn2+ and Cd2+.  相似文献   

3.
The adsorption behavior of Zn2+ ions onto the surface of amorphous aluminosilicates was studied using both potentiometric and spectroscopic methods (XANES: X-ray Absorption Near-Edge Structure). The aluminosilicates were prepared with different Al/Si ratios in order to compare the reactivities of surface aluminol and silanol groups toward Zn2+ ions. Potentiometric experiments were performed by maintaining the reacting suspensions at constant pH, ionic strength, and solid concentration, while Zn concentration was increased by stepwise addition. Our results showed that the surface aluminol and silanol groups possess significantly different reactivities toward Zn2+ ions. The reaction of Zn2+ ions with aluminol groups occurs through three processes: (i) surface complexation, (ii) dissolution, and (iii) re-sorption. A stoichiometric relationship was confirmed for the surface complexation between the aluminol groups and Zn2+ ions: two moles of H+ ions were released for one mole of Zn2+ ion adsorption. Following the surface complexation process, measurable amounts of zinc and aluminum ions were found to be mobilized from the surface of the solid to the liquid phase; subsequently, these ions precipitated on the solid surface, and possibly formed a co-precipitate with the hydrotalcite-type structure. On the other hand, a stoichiometric relationship was not obtained for the sorption of Zn2+ ions on silanol groups, and therefore, it was concluded that Zn2+ ions are retained on the surface of amorphous aluminosilicates by two different reactions. One reaction involves the surface complexation between Zn2+ ions and surface aluminol groups, which proceeds rapidly. The other reaction is the slow retention of Zn2+ ions onto silanol and/or aluminol groups, which could be the surface precipitation of Zn(OH)2 or the co-precipitation of Zn2+-Al3+ hydroxides. It can be suggested that the total sorption behavior of Zn2+ ions on amorphous aluminosilicates with different Al/Si ratios can be represented as the sum of the individual reactions of Zn2+ ions toward the aluminol and silanol groups. The potentiometric results were confirmed by XANES data. It was clearly evident that only the aluminol groups were responsible for surface complexation of Zn2+ ions. An equilibrium constant was calculated for this reaction.  相似文献   

4.
A central composite face-centered design was used to study and to optimize lead biosorption from aqueous solution on Aspergillus terreus biomass. Four factors such as stirring speed, temperature, solution pH and biomass dose at different levels were studied.The hierarchical quadratic model were established by adding replicates at the central point and axial points to the initial full factorial design (24). The percentage removal of lead was affected by biomass dose, pH, and interactions between pH and biomass dose, pH and stirring speed, pH and temperature. The hierarchical quadratic model described adequately the response surface based on the adjusted determination coefficient (R2 Adj= 0.97) and the adequate precision ratio (42.21). According to this model, the optimal conditions to remove lead completely from aqueous solutions (at initial lead concentration of 50 mg/L and solutions of 100 mL) with Aspergillus terreus were at pH 5.2, 50 °C, stirring speed of 102/min and a biomass dose of 139 mg.The response surface methodology can be used to determine the optimal conditions for metal adsorption on several adsorbents. In addition, results reported in this research demonstrated the feasibility of employing A. terreus as biosorbent for lead removal.  相似文献   

5.
Peganum harmala seeds were assessed as biosorbent for removing Pb2+, Zn2+and Cd2+ ions from aqueous solutions. The effects of various parameters such as the aqueous solution pH, the contact time, the initial metal concentration and the amount of adsorbent in the process were investigated. The adsorption efficiencies increased with pH. It was found that about 95 % of lead, 75 % of zinc and 90 % of cadmium ions could be removed from 45 ml of aqueous solution containing 20 mg l?1 of each cation with 2 g of adsorbent at pH 4.5 after 15 min. The quantitative desorption of cadmium from adsorbent surface was achieved using 10 ml of a 0.5 M nitric acid solution. This condition was attained for lead and zinc ions with 10 ml of 1 M hydrochloric acid solution. Kinetic investigation of the process was performed by considering a pseudo-second-order model. This model predicts the chemisorption mechanism of the process. Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models were tested for describing the equilibrium data. It was found that the Freundlich model describes the experimental data resulting from the adsorption of lead ions. However for cadmium and zinc ions, the adsorption equilibria were interpreted with the Langmuir model.  相似文献   

6.
The application of organic-rich lake sediment (gyttja) to exploration geochemistry is discussed. Gyttja was collected from some 42 lake sites in the Red Lake-Uchi Lake volcanic-sedimentary sequences.The existance of free sulphide ion in most gyttja is confirmed and theoretical calculations are used to define the approximate concentrations of sulphide ion which determine whether the accumulation of Cu+, Cu2+, Zn2+ and Fe2+ is by metal sulphide precipitation, organic complexing or both. These calculations show that in the sediments collected in this study, the accumulation of copper will probably be by metal sulphide formation, whereas for zinc, organic complexing and possibly sulphide precipitation are likely mechanisms.It is shown that the background concentrations of copper and zinc on a dry matter basis increase with the content of organic matter in the sediment and it is further shown that the quantity of interstitial water in the sediment increases linearly with the organic content. Also it is demonstrated that the organic matter in the sediment is dispersed in the interstitial water in approximately the same concentration irrespective of the sediment composition.On the assumption that copper sulphide colloids are dispersed in the interstitial water of the sediment, it is suggested that the copper content of gyttja should be expressed as μg/g interstitial water for meaningful interpretation. Similarly, the zinc content should be expressed relative to the organic matter content.The ability of reagents to selectively extract only chemically dispersed metals and not silicate lattice metals from gyttja is discussed.Both the analytical procedures and the interpretations are applied to the samples collected.  相似文献   

7.
Nile Rose Plant was used to study adsorption of several cations (Cu2+, Zn2+, Cd2+ and Pb2+) from wastewater within various experimental conditions. The dried leaves of Nile Rose Plant were used at different adsorbent/ metal ion ratios. The influence of pH, contact time, metal concentration, and adsorbent loading weight on the removal process was investigated. Batch adsorption studies were carried out at room temperature. The adsorption efficiencies were found to be pH dependent, increasing by increasing the pH in the range from 2.5 to 8.5 exept for Pb. The equilibrium time was attained within 60 to 90 min. and the maximum removal percentage was achieved at an adsorbent loading weight of 1.5 g/50 mL mixed ions solution. Isothermal studies showed that the data were best fitted to the Temkin isotherm model. The removal order was found to be Pb2+> Zn2+> Cu2+> Cd2+. The surface IR-characterization of Nile rose plant showed the presence of many functional groups capable of binding to the metal cations.  相似文献   

8.
Experiments of Zn2+ and Fe3+ coprecipitation as a function of pH were conducted in the laboratory at ambient temperature and pressure. X-ray diffraction patterns of the coprecipitates show two broad peaks at 0.149 and 0.258 nm, which is consistent with published patterns for pure 2-line ferrihydrite. Zn2+ uptake occurred at pH ≥5 while Fe3+ precipitation occurred between pH 3 and 4, although both Zn2+ and Fe3+ were present in the same solution during the entire range of pH titration. High-resolution transmission electron microscopy shows that the coprecipitates are 2 to 6 nm sized single crystalline particles but aggregated to 50 to 400 nm sized clusters. Analytical electron microscopy indicated that the 5% atomic Zn with respect to Fe was homogeneously distributed. No segregated phases were found in the clusters or at single crystal edges, which is consistent with published extended X-ray absorption fine structure (EXAFS) results at similar Zn/(Zn + Fe) ratios. Hence, occlusion and surface precipitation may be excluded as possible coprecipitation mechanisms. The bulk solution Zn2+ sorption edge was fitted to both solid solution and generalized diffuse layer surface complexation models. However, a solid solution model is inconsistent with published EXAFS results that show tetrahedral polydentate Zn2+ complexes sharing apices with Fe3+octahedra.  相似文献   

9.
In this study, the dissolution of magnesite particles in aqueous lactic acid solutions was investigated in a batch reactor employing the parameters of stirring speed, particle size, temperature and acid concentration. The shrinking core model was evaluated to determine the effect of particle size, temperature and concentration. It was also found that the stirring speed did not change the dissolution. Consequently, it was determined that the dissolution rate is controlled by surface chemical reaction. The activation energy of the process was determined to be 50.3 kJ mol− 1.  相似文献   

10.
Cadmium and zinc were added at 3 and 300 mg kg−1, respectively, to 23 soils and incubated at 16°C and 80% field capacity for 818 d. Following addition of metal, changes in the radio-labile concentrations of both elements were examined on seven separate sampling occasions over 818 d. At each sample time, soil pore water was extracted using Rhizon soil solution samplers, and concentrations of Cd, Zn, dissolved organic carbon, and major cations and anions were determined. The chemical speciation program WHAM 6 was used to determine free metal ion activity, (M2+). Similar measurements were made on a set of historically contaminated soils from old mining areas, sewage sludge disposal facilities, and industrial sources. The two data sets were combined to give a range of values for p(Cd2+) and p(Zn2+) that covered 5 and 4 log10 units, respectively. A pH-dependent Freundlich model was used to predict Zn2+ and Cd2+ ion activity in soil pore water. Total and radio-labile metal ion concentration in the solid phase was assumed to be adsorbed on the “whole soil,” humus, or free iron oxides to provide alternative model formats. The most successful models assumed that solubility was controlled by adsorption on soil humus. Inclusion of ionic strength as a model variable provided small improvements in model fit. Considering competition with Ca2+ and between Zn2+ and Cd2+ produced no apparent improvement in model fit. Surprisingly, there was little difference between the use of total and labile adsorbed metal as a model determinant. However, this may have been due to a strong correlation between metal lability and pH in the data set used. Values of residual standard deviation for the parameterized models using labile metal adsorbed on humus were 0.26 and 0.28 for prediction of p(Cd2+) and p(Zn2+), respectively. Solubility control by pure Zn and Cd minerals was not indicated from saturation indices. However there may have been fixation of metals to non-radio-labile forms in CaCO3 and Ca-phosphate compounds in the soils in the higher pH range. Independent validation of the Cd model was carried out using an unpublished data set that included measurements of isotopically exchangeable Cd. There was good agreement with the parameterized model.  相似文献   

11.
Adsorption of Zn2+ at the rutile TiO2 (110)-aqueous interface was studied with Bragg-reflection X-ray standing waves (XSW), polarization-dependent surface extended X-ray absorption fine structure (EXAFS) spectroscopy, and density functional theory (DFT) calculations to understand the interrelated issues of adsorption site, its occupancy, ion-oxygen coordination and hydrolysis. At pH 8, Zn2+ was found to adsorb as an inner-sphere complex at two different sites, i.e., monodentate above the bridging O site and bidentate between two neighboring terminal O sites. EXAFS results directly revealed a four or fivefold first shell coordination environment for adsorbed Zn2+ instead of the sixfold coordination found for aqueous species at this pH. DFT calculations confirmed the energetic stability of a lower coordination environment for the adsorbed species and revealed that the change to this coordination environment is correlated with the hydrolysis of adsorbed Zn2+. In addition, the derived adsorption locations and the occupancy factors of both sites from three methods agree well, with some quantitative discrepancies in the minor site location among the XSW, EXAFS, and DFT methods. Additional XSW measurements showed that the adsorption sites of Zn2+ were unchanged at pH 6. However, the Zn2+ partitioning between the two sites changed substantially, with an almost equal distribution between the two types of sites at pH 6 compared to predominantly monodentate occupation at pH 8.  相似文献   

12.
Readily dispersible clay is the part of the clay fraction in soils that potentially disperses in water when a small amount of mechanical energy is applied to soil. Column and batch experiments were conducted to identify the effect of readily dispersible clay on the mobility of some metal ions in a disturbed soil sample. The clay fraction (<0.002 mm) was separated from an alkaline Vertisol from the Nile River Delta. X-ray diffraction technique was used to identify minerals present in the clay fraction. Clay suspensions and deionized H2O solutions of Cd2+, Cu2+, and Zn2+ were prepared and used as influents in soil columns. Adsorption capability of the studied soil among the three metal ions was investigated. The results showed high adsorption capacity of Cd2+, Cu2+, but not Zn2+ for the studied soil. Cu2+ was the highest adsorbed metal by soil and its sorption increased at small equilibrium concentrations compared with Cd2+ and Zn2+. For the three studied metal ions, Langmuir model represented the best fit to the adsorption data. The concentration of Zn2+ and Cd2+ in leachates increased as the leaching solution volume increased, while Cu2+ showed a homogeneous distribution throughout the soil column. According to DTPA extractable metals, Zn2+ was appeared at greater depths than Cd2+, while Cu2+ had homogeneous distribution through the soil column.  相似文献   

13.
Homogenized samples of raw clays resulting from two (2) different lots of natural clays from Maghnia (Algeria) have been assessed for their potential use in the removal of Pb2+ and Zn2+ ions from industrial liquid wastes (LW). Raw and acid-activated samples have been characterized by powder X-ray diffraction, FT-IR spectroscopy, electron microscopy (SEM), and X-ray fluorescence (XRF) and used as adsorbents for the removal of Pb2+ and Zn2+ ions from aqueous system using adsorption method under different conditions. The effect of factors including contact time, pH, and dosage on the adsorption properties of Pb2+ and Zn2+ ions onto clays was investigated at 25 °C. The obtained results revealed that the removal percentages of Pb2+ and Zn2+ ions, from both aqueous solution (AS) and LW, were varying between 90 and 98% for 40 min and optimal pH values ranged from 5 to 6 for Pb2+ and Zn2+ ions, respectively. The kinetics of both Pb2+ and Zn2+ ion adsorption fitted well with the pseudo-second-order model. Langmuir, Freundlich, and Temkin adsorption isotherms were used, and their constants were evaluated. The values of thermodynamic parameters, ΔH°, ΔS°, and ΔG° indicated that the adsorption of Pb2+ and Zn2+ ions was spontaneous and exothermic process in nature. The adsorption and desorption isotherms indicated that Pb2+ and Zn2+ adsorption to raw clays was reversible. The experimental results obtained showed that the raw clays from Maghnia (Algeria) had a great potential for removing Pb2+ and Zn2+ ions from industrial liquid wastes using adsorption method.  相似文献   

14.
在环境温度下,水中Cu^2+与铁硫化物矿物交换反应形成的铜蓝的结晶度可以影响Cu^2+的回收效率及交换反应的完全程度。本文利用Cu Cl2和Na2S直接反应生成铜蓝,讨论了不同p H值、反应时间、反应温度、反应物浓度、反应物滴加速度、外加电解质浓度等条件对铜蓝晶体生长的影响,并采用XRD、TEM和EDX方法对铜蓝结晶度和形貌进行了表征,用Scherrer公式计算了晶体的平均粒径。结果表明,反应p H值越低,时间越长,温度越高,反应物滴加速度越慢,越有利于铜蓝晶体生长;铜蓝晶体结晶度随着反应物浓度的增加呈先增后减的趋势,而在不同外加电解质浓度条件下表现出不同的结晶度。  相似文献   

15.
Biosorption is a promising technology for the removal of heavy metals from industrial wastes and effluents. In the present study, biosorption of Pb2+, Cu2+, Fe2+ and Zn2+ onto the dried biomass of Eucheuma denticulatum (Rhodophyte) was investigated as a function of solution pH, contact time, temperature and initial metal ion concentration. The experimental data were evaluated by Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The sorption isotherm data followed Langmuir and Freundlich models, and the maximum Langmuir monolayer biosorption capacity was found as 81.97, 66.23, 51.02 and 43.48 mg g?1 for Pb2+, Cu2+, Fe2+ and Zn2+, respectively. The sorption kinetic data followed pseudo-second-order and intraparticle diffusion models. Thermodynamic study revealed feasible, spontaneous and endothermic nature of the sorption process. Fourier transform infrared analysis showed the presence of amine, aliphatic, carboxylate, carboxyl, sulfonate and ether groups in the cell wall matrix involved in metal biosorption process. A total of nine error functions were applied in order to evaluate the best-fitting models. We strongly suggest the analysis of error functions for evaluating the fitness of the isotherm and kinetic models. The present work shows that E. denticulatum can be a promising low-cost biosorbent for removal of the experimental heavy metals from aqueous solutions. Further study is warranted to evaluate its potential for the removal of heavy metals from the real environment.  相似文献   

16.
Removal of arsenite from aqueous solution was carried out using electro-coagulation method. The experiments were conducted using copper–copper and zinc–zinc electrodes. The optimized experimental parameters were 2.0 mg/L initial concentration, 16.0-min processing time, 6.0 pH, 3.0-V applied voltage and 30 °C temperature for zinc–zinc electrodes while these values for copper–copper electrodes were 2.0 mg/L initial concentration, 20.0-min processing time, 7.0 pH, 5.0-V applied voltage and 30 °C temperature. The results demonstrated that zinc–zinc and copper–copper electrodes removed arsenite up to 99.89 and 99.56 %, respectively. The treated water was clear, colorless and odorless without any secondary contamination. There was no change in water quality after the removal of arsenite. The reported method is capable to remove arsenite from water at 6–7 pH range, which is a pH range of natural water. Therefore, this method may be the choice of arsenite removal from natural ground water.  相似文献   

17.
Granular activated carbon produced from palm kernel shell was used as adsorbent to remove copper, nickel and lead ions from a synthesized industrial wastewater.Laboratory experimental investigation was carried out to identify the effect of pH and contact time on adsorption of lead, copper and nickel from the mixed metals solution. Equilibrium adsorption experiments at ambient room temperature were carried out and fitted to Langmuir and Freundlich models. Results showed that pH 5 was the most suitable, while the maximum adsorbent capacity was at a dosage of 1 g/L, recording a sorption capacity of 1.337 mg/g for lead, 1.581 mg/g for copper and 0.130 mg/g for nickel. The percentage metal removal approached equilibrium within 30 min for lead, 75 min for copper and nickel, with lead recording 100 %, copper 97 % and nickel 55 % removal, having a trend of Pb2+ > Cu2+ > Ni2+. Langmuir model had higher R2 values of 0.977, 0.817 and 0.978 for copper, nickel and lead respectively, which fitted the equilibrium adsorption process more than Freundlich model for the three metals.  相似文献   

18.
Heavy metal ions (Pb2+, Cd2+, Ni2+, and Zn2+) were biosorbed by brown seaweed (Hizikia fusiformis), which was collected from Jeju Island of South Korea. The metal adsorption capacity of H. fusiformis improved significantly by washing with water or by base or acid treatments. The maximum sorption by NaOH-pretreated biomass was observed near a slightly acidic pH (pH 4?6) for Pb2+, Cd2+, Ni2+, and Zn2+. This result suggests that the treatment of H. fusiformis biomass with NaOH helped increase the functional forms of carboxylate ester units. Kinetic data showed that the biosorption occurred rapidly during the first 60 min, and most of the heavy metals were bound to the seaweed within 180 min. The maximum metal adsorption capacities assumed by a Langmuir model were on the order of Pb2+ > Cd2+ > Ni2+ > Zn2+. Equilibrium adsorption data for the heavy metal ions could fit well in the Langmuir model with regression coefficients R 2 > 0.97.  相似文献   

19.
The batch removal of copper(II) ions from aqueous solution under different experimental conditions using alkali-leached silica and activated charcoal was investigated in this study. The copper(II) uptake was dependent on varying time, pH, copper concentration and temperature. Copper sorption was found fast reaching equilibrium within 1 h with better performance for alkali-leached silica than charcoal. Copper sorption was low at low pH values and increased with rise in initial pH-value until 6.7. Sorption fits well the Langmuir and Freundlich equations with higher uptake by increasing temperature. According to Langmuir equation, the maximum uptake of Cu(II) ions by alkali-leached SiO2 and charcoal was found to be 242.5 and 94.4 mmol/g at temperature 60 °C and pH 6. Thermodynamic studies confirm that the process was spontaneous and endothermic nature. Kinetic data for Cu(II) sorption was found to follow pseudo-second-order model.  相似文献   

20.
The sorption of ferrous iron to a clay mineral, nontronite (NAu-2, a ferruginous smectite), was investigated under strictly anoxic conditions as a function of pH (3-10), Fe2+ concentration (0.01-50 mM), equilibration time (1-35 days), and ionic strength (0.01-0.5 M NaClO4). The surface properties of NAu-2 were independently characterized to determine its fixed charge and amphoteric site density in order to interpret the Fe2+ sorption data. Fe2+ sorption to NAu-2 was strongly dependent on pH and ionic strength, reflecting the coupled effects of Fe2+ sorption through ion exchange and surface complexation reactions. Fe2+ sorption to NAu-2 increased with increasing pH from pH 2.5 to 4.5, remained constant from pH 4.5 to 7.0, increased again with further increase of pH from pH 7.0 to 8.5, and reached a maximum above pH 8.5. The Fe2+ sorption below pH 7.0 increased with decreasing ionic strength. The differences of Fe2+ sorption at different ionic strengths, however, diminished with increasing equilibration time. The Fe2+ sorption from pH 4.5 to 7.0 increased with increasing equilibration time up to 35 days and showed stronger kinetic behavior in higher ionic strength solutions. The kinetic uptake of Fe2+ onto NAu-2 is consistent with a surface precipitation mechanism although our measurements were not able to identify secondary precipitates. An equilibrium model that integrates ion exchange, surface complexation and aqueous speciation reactions reasonably well describes the Fe2+ sorption data as a function of pH, ionic strength, and Fe2+ concentration measured at 24 h of equilibration. Model calculations show that the species Fe(OH)+ was required to describe Fe2+ sorption above pH 8.0 satisfactorily. Overall, this study demonstrated that Fe2+ sorption to NAu-2 is affected by complex equilibrium and kinetic processes, likely caused by surface precipitation reactions.  相似文献   

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