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1.
The complex micro-interfacial interaction theories of heavy metal ions such as Pb(II) and Cd(II)adsorption on fine sediment in aqueous solution were not systematically investigated. The aim of this work was to reflect the micro-interfacial adsorption characteristics. Sediment samples were collected from an estuary. The Isothermal and kinetics adsorption experiment were done to acquire the data.Isothermal, kinetics, film diffusion and intraparticle diffusion models were adopted to fit the adsorption experimental data. The results indicated that the Langmuir, Freundlich and Temkin models were suitable for analyzing the isothermal experimental data. The maximum adsorption capacities of Pb(II) and Cd(II)on the sediment were 1.1377 and 0.9821 mg·g_(-1), respectively. The q_m and K_L of the Langmuir model, K_f and n_F of the Freundlich model, and b and A of the Temkin model all exhibited a power function relationship with the initial adsorbate concentration. The pseudo-second-order model provided a better fit for the experimental kinetics data compared with the fit of the pseudo-first-order and Elovich models.The pseudo-second-order parameters k_2 and q_e of Pb(II) and q_e of Cd(II) both had a power function relationship with adsorption time, additionally, the k_2 of Cd(II) had an exponential function relationship with adsorption time. The liquid-film diffusion parameters k_(fd) of Pb(II) and Cd(II) were 0.0569 and 0.1806 min_(-1), respectively. The intraparticle diffusion parameter k_(id) values of Pb(II) and Cd(II) were0.0055 mg·g_(-1)·min_(1/2) and 0.0049 mg·g_(-1)min_(1/2), respectively. The physical significance of the model parameters showed that Pb(II) adsorption on sediment was stronger than Cd(II). The results of this study provided a theoretical reference for the micro-interfacial mechanism of heavy metal ion adsorption on sediment.  相似文献   

2.
The adsorption of cobalt ions was evaluated using sediment samples from water bodies to investigate the adsorption properties of sediment and the behavior of these natural materials in the presence of nuclear and industrial waste.The two sediments(S1 and S2)were treated to eliminate humic and fulvic acids and then they were characterized by several techniques.The minerals found in both the sediments(X-ray diffraction)were quartz and albite;plus,goethite and muscovite in S1,and kaolinite and montmorillonite in S2.Point of zero charge(PZC)of S1 and S2 was 6.00 and 5.22,respectively.The specific area of S1(63.3 m2/g)is higher than S2(1.5 m2/g).Adsorption kinetics data for S1 and S2 were best fitted to the pseudo second-order model.The removal efficiency of S1 for cobalt was 96%with an adsorption capacity(qe)of 0.93 mg/g,and for S2 was 45%with a qeof 0.40 mg/g.The experimental data of the adsorption isotherms were adjusted to Langmuir and Freundlich models for S1 and S2,respectively.The thermodynamic parameters(enthalpy,entropy,and Gibb’s free energy)indicated that the adsorption processes were endothermic,spontaneous,and chemisorption mechanism.The results show that the adsorption capacities of the sediments depend on their composition.These water sediments have important adsorption properties for cobalt,and they can be used in the treatment of nuclear and industrial aqueous wastes.  相似文献   

3.
Adsorption behaviors of acetaminophen onto sediment in the Weihe River were described.The impact factors in the processes of adsorption,such as contact time,solution pH,temperature,and ionic strength,were determined by experiments.The experimental results were analyzed by kinetic and isotherm models.The adsorption kinetics was found to follow a pseudo-first-order model.The equilibrium adsorption data fitted well with the Langmuir and Freundlich isotherm models.However,the Langmuir isotherm was more suitable to describe the adsorption.Thermodynamics parameters such as Gibbs-free energy change(△C~0),enthalpy change(△H~0) and entropy change(△S~0) were calculated.Results showed that the adsorption was feasible,spontaneous,entropy increasing,and endothermic in nature,which reached equilibrium in about 24 hours.The adsorption capacity did not cause obvious change at solution pH 3.0-9.0,and decreased in solution pH 9.0-11.0.The presence of electrolytes such as NaCl in aqueous solution had a significant negative effect on the adsorption.The mechanisms controlling the adsorption were supposed to be chemisorption.  相似文献   

4.
The sediment deposited behind a dam(DS) and its inorganic materials(IM-DS) were characterized and used for the removal of praseodymium(Pr) from aqueous solutions. Quartz, albite, and kaolinite were found in the sediment by X-ray diffraction. Kinetic data fit well to a pseudo second-order model, the equilibrium time for DS and IM-DS was 2 h and 3 min, respectively, and the adsorption capacity was higher for Pr/DS(qe= 4.91 mg/g) than for Pr/IM-DS(qe= 3.01 mg/g) in these condi...  相似文献   

5.
Arsenic(As) contamination in groundwater is a major problem in many countries, which causes serious health issues. In this paper, a novel method has been developed for the simultaneous removal of ROX and As(Ⅲ/Ⅴ) using the modified sorghum straw biochar(MSSB). The MSSB was characterized by X-ray diffraction, scanning electron microscopy, Fourier Transform Infrared, and Brunauer–Emmet–Teller(BET) surface area.The removal performance of MSSB for ROX, arsenite[As(Ⅲ)], and arsenate(As(Ⅴ)) was investigated using batch experiments. At pH of 5, the arsenic concentration of 1.0 mg/L, adsorbent dose of 1.0 g/L, the maximum adsorptioncapacities of ROX,As(Ⅲ),and As(Ⅴ) were 12.4, 5.3, and 23.0 mg/g, respectively. The adsorption behaviors were fit well with the Langmuir and the pseudo-second-order rate model. The results showed that MSSB acted as a highly effective adsorbent to simultaneously remove the composite pollution system consisted of ROX and As(Ⅲ/Ⅴ) in aqueous solutions,providing a promising method in environmental restoration applications.  相似文献   

6.
A two-dimensional mathematical model for simulating flow and sediment transport is presented. The model simulates flow and geo-morphological processes using a high order accurate, oscillation free scheme. The depth averaged Reynolds (shallow water) equations are used for flow simulation. Both equilibrium and non-equilibrium methods (by solving convection-diffusion equation) are used for sediment transport modeling while sediment carrying capacity is computed using different methods. A finite volume, flux difference splitting scheme is employed to solve the governing equations, which is able to simulate sub, super and transeritical flows with shock waves. Moreover, the numerical method is able to simulate flow over the variable topographies and it has a low level of numerical diffusion in the case of circulating flows like headlands. The computational grid of this model is triangular unstructured with variable size, which is flexible for arbitrary geometries and grid refinement. Using the model for simulating flow and sediment transport in some test cases such as a partially closed channel and comparing the results showed that the results obtained by the developed model were in a reasonable agreement with measurements and the other models cited.  相似文献   

7.
《国际泥沙研究》2016,(2):139-148
Applications of sediment transport and water flow characteristics based sediment transport simulation models for a river system are presented in this study. An existing water–sediment model and a new sediment–water model are used to formulate the simulation models representing water and sediment movement in a river system. The sediment–water model parameters account for water flow characteristics embodying sediment transport properties of a section. The models are revised formulations of the multiple water inflows model describing water movement through a river system as given by the Muskingum principle. The models are applied to a river system in Mississippi River basin to estimate downstream sediment concentration, sediment discharge, and water discharge. River system and the river section parameters are estimated using a revised and the original multiple water inflows models by applying the genetic algorithm. The models estimate downstream sediment transport rates on the basis of upstream sediment/water flow rates to a system. Model performance is evaluated by using standard statistical criteria;downstream water discharge resulting from the original multiple water inflows model using the estimated river system parameters indicate that the revised models satisfactorily describe water movement through a river system. Results obtained in the study demonstrate the applicability of the sediment transport and water flow characteristics-based simulation models in predicting downstream sediment transport and water flow rates in a river system.  相似文献   

8.
Pollutants are carried by sediment-laden flow dissolved in water or adsorbed on sediment particles. A transient three-dimensional model based on a compressible VOF(volume of fluid) method was developed to simulate the transport of dissolved and particulate pollutants.VOF is a numerical technique for acquiring and tracking the free surface of water flow.Local scouring,deposition and re-suspension were simulated and the processes of adsorption and desorption of pollutants on suspended sediment were analyzed.A series of experiments and numerical simulations were performed to study the transportation and dispersion of pollutants in the flow around a non-submerged spur dyke in a straight flume of rectangular shape.The simulation results agreed well with the experimental results.A certain volume of pollutants solution was released into the flow at upstream of the spur dyke.The concentration reduced with time.The concentration reduction was slower in the circumfluence zone than in the main flow.The ratio of adsorption to desorption coefficients was different for pollutants on suspended sediment with different diameter.The peak concentration of dissolved pollutants increased with the ratio of the adsorption to the desorption coefficients.The angle of the spur dyke affected the peak concentration around the dyke.The effect of the angle on dissolved pollutants decreased with the ratio of adsorption to desorption coefficients.The adsorption and desorption coefficients,as well as the saturated adsorption capacity had no effect on the concentration of particulate pollutants.  相似文献   

9.
Evaluating the benefits of sediment and runoff reduction in different vegetation types is essential for studying the mechanisms of soil and water conservation on the Loess Plateau.The experiment was conducted in shrub-grass plots with nine levels of mixed vegetation coverage from 0%to 70%,three slopes(10,15,and 20)and two rainfall intensities(1.0 and 2.5 mm/min).The results showed that the vegetation coverage and slope gradient significantly affect runoff and sediment yield.Shrub-grass vegetation coverage had a significant effect on the runoff start-time,runoff flow velocity,runoff rate,and soil erosion rate on hillslopes.Mixed vegetation coverage could effectively delay the runoff starttime and decrease the runoff flow velocity.However,the effects of the slope gradient on runoff and sediment yield are opposite to those of vegetation coverage.Shrub-grass vegetation coverage could effectively increase runoff and sediment yield reduction benefits,while their benefits were affected by the rainfall intensity.At the 1.0 mm/min rainfall intensity,the reduction in the sediment production rate was greater than that under the 2.5 mm/min intensity.However,when the shrub-grass vegetation coverage exceeded 42%,the runoff reduction benefit was more obvious at higher rainfall intensities.The cumulative sediment yield increased with increasing cumulative runoff,and the rate of increase in the cumulative runoff was greater than that of the cumulative sediment yield with increasing of shrub-grass vegetation coverage.Moreover,there was a power function relationship between cumulative sediment yield and cumulative runoff yield(P<0.05).Our paper is expected to provide a good reference on the ecological environment and vegetation construction on the Loess Plateau.  相似文献   

10.
Modeling of suspended sediment particle movement in surface water can be achieved by stochastic particle tracking model approaches.In this paper,different mathematical forms of particle tracking models are introduced to describe particle movement under various flow conditions,i.e.,the stochastic diffusion process,stochastic jump process,and stochastic jump diffusion process.While the stochastic diffusion process can be used to represent the stochastic movement of suspended particles in turbulent flows,the stochastic jump and the stochastic jump diffusion processes can be used to describe suspended particle movement in the occurrences of a sequence of extreme flows.An extreme flow herein is defined as a hydrologic flow event or a hydrodynamic flow phenomenon with a low probability of occurrence and a high impact on its ambient flow environment.In this paper,the suspended sediment particle is assumed to immediately follow the extreme flows in the jump process(i.e.the time lag between the flow particle and the sediment particle in extreme flows is considered negligible).In the proposed particle tracking models,a random term mainly caused by fluid eddy motions is modeled as a Wiener process,while the random occurrences of a sequence of extreme flows can be modeled as a Poisson process.The frequency of occurrence of the extreme flows in the proposed particle tracking model can be explicitly accounted for by the Poisson process when evaluating particle movement.The ensemble mean and variance of particle trajectory can be obtained from the proposed stochastic models via simulations.The ensemble mean and variance of particle velocity are verified with available data.Applicability of the proposed stochastic particle tracking models for sediment transport modeling is also discussed.  相似文献   

11.
This study aims to remove of Cu2+, Cd2+, and Pb2+ ions from solution and to investigate the adsorption isotherms, adsorption kinetics, and ion‐exchange affinities of these metals using waste activated sludge (AS) biomass. The adsorptions of the metals on biomass were optimal at an acidic pH value of 6.0 based on its monolayer capacities. Maximum monolayer capacities of AS biomass (qmax) were calculated as 0.478, 0.358, and 0.280 mmol g?1 for Cu2+, Cd2+, and Pb2+, respectively, and the adsorption equilibrium time was found as 60 min for each metal. The adsorbed amount of metal rose with increasing of initial metal ion concentration. The equilibrium adsorption capacity of AS for initial 0.25 mmol L?1 metal concentration was determined as 0.200, 0.167, and 0.155 mmol g?1 for Cu2+, Cd2+, and Pb2+ ions, respectively. These relevant values were determined as 0.420, 0.305, and 0.282 mmol g?1 for Cu2+, Cd2+, and Pb2+ ions, respectively, when initial metal concentration was 0.50 mmol L?1. In the multi‐metal sorption system, the adsorption capacity of AS biomass was observed in the order of Cu2+ > Cd2+ > Pb2+. In the presence of 100 mmol L?1 H+ ion, the order of ion‐exchange affinity with H+ was found as Cu2+ > Cd2+ > Pb2+. The adsorption kinetics were also found to be well described by the pseudo‐second‐order and intraparticle diffusion models. Two different rate constants were obtained as ki1 and ki2 and ki1 (first stage) was found to be higher than ki2 (second stage).  相似文献   

12.
The effects on phytoplankton photosynthesis of inorganic metal salts HgCl2, CuSO4, Cd(NO3)2, ZnCl2 and Pb(NO3)2 were studied over monthly intervals. In experiments with individual metals, phytoplankton photosynthesis was not adversely affected if the concentration increase above background levels did not exceed 10?9 mole Hg/l, 5·10?9 mole Cu/l, 2·10?8 mole Cd/l, 5·10?8 mole Zn/l and 2·10?7 mole Pb/l, respectively. However when the concentration was increased by 5·10?10 mole Hg/l+5·10?9 mole Cu/l+5·10?9 mole Cd/l+5·10?8 mole Zn/l+5·10?8 mole Pb/l photosynthesis was significantly reduced, due to a synergetic effect of the combined metals. The influence of phytoplankton density, pH-value concentration of calcium, dissolved organic nitrogen and allochthonous debris on heavy metal toxicity was investigated. Changes in phytoplankton composition are believed to the main reason for the seasonal variation in the toxic effects of heavy metals.  相似文献   

13.
In order to investigate the pollution levels, sources and ecological risks of arsenic (As) and heavy metals (Cr, Ni, Cu, Zn, Pb and Cd) in inshore sediments of the Yellow River estuary, the surface sediment in areas of inshore coastal waters were sampled in October 2014 as the flow-sediment regulation project (FSRP) was implemented for 13 years. Results showed that the concentrations of As and heavy metals in inshore sediments of the Yellow River estuary were in the order of Zn?>?Cr?>?Cu?>?Ni?>?Pb?>?As?>?Cd. Higher levels of As, Cr, Ni, Cu, Zn and Pb generally occurred in fine-grained sediments of the Yellow River estuary and the southeast region, which was consistent with the spatial distribution of clay. In contrast, higher concentrations of Cd were generally observed in northwest area of the Yellow River estuary and near the Qingshuigou estuary, which showed similarly spatial distribution with that of sand. The sediment quality guidelines (SQGS) and geoaccumulation indices (Igeo) indicated that the inshore sediments were polluted by Cu, Cd, As, Pb and Zn, and, among them, Cd pollution was more serious. Ecological risk indices (E r i ) demonstrated low risks for Cr, Ni, Cu, Zn, Pb and As, and high potential toxicity by Cd. The integrated ecological risk index implied that 6.8% of stations presented moderate risk, 4.5% of stations exhibited disastrous risk, and 88.7% of stations demonstrated considerable risk. Principal component analysis indicated that Ni, Cu, Zn, Pb and As might originate from common pollution sources, while Cr and Cd might share another similar sources. With the continuous implementation of FSRP, As and heavy metal levels in inshore sediments of the Yellow River estuary could be classified as stage I (2002–2010) and stage II (2010–2014). In the stage I, As, Cr, Ni, Cu, Zn and Pb levels fluctuated but decreased significantly, whereas Cd concentrations showed little variation. In the stage II, As and heavy metal levels significantly increased although some little fluctuations occurred. The continuous accumulation of As and heavy metals (especially for Cd) in inshore sediments of the Yellow River estuary would occur again as the FSRP was implemented for 9 years (since 2010). The ecotoxicological risk of Cd, As, Ni and Cu in inshore sediments might be more serious since the accumulation of the four elements would be continuously occurred in future years. Next step, there will be long-term potential consequences for marine organism if effective measures are not taken to control the loadings of metal pollutants into estuary.  相似文献   

14.
Water quality data collected on a fortnightly or monthly basis are inadequate for assessment and modelling of many water quality problems as storm event samples are underrepresented or missed. This paper examines the stormflow dynamics of heavy metals (Pb, Cu, Cd and Zn) in the Nant‐y‐Fendrod stream, South Wales, which has been affected by 250 years of metal smelting, followed by 35 years of landscape rehabilitation measures. For storm events of contrasting (very dry and very wet) antecedent conditions in May 2000 and February 2001, respectively, temporal changes in streamwater heavy metal concentrations above and below an in‐line flood detention lake are analysed. At the upstream site, peaks in total metal concentration were recorded on the rising limb for Pb (0·150 mg l?1) and Cu (0·038 mg l?1) but on the falling limb for Zn (1·660 mg l?1) and Cd (0·006 mg l?1) in the summer 2000 storm event, yielding clockwise and anticlockwise hysteretic loops respectively. In contrast, metal concentrations, although high throughout the winter storm event, were diluted somewhat during the storm peak itself. The Pb and Cu appear to be supplied by quickflow processes and transported in close association with fine sediment, whereas Zn and Cd are delivered to the channel and lake by slower subsurface seepage in dissolved form. In the winter 2001 event, antecedent soil moisture and shallow groundwater levels were anomalously high and seepage sources of dissolved metals dominated. Downstream of the lake, Pb and Cu levels and suspended sediment were high in the summer storm, but low in the winter storm, suggesting retention with deposition of fine sediment in the lake during the latter. In the winter storm, Zn and Cd levels were higher downstream than upstream of the lake, perhaps because of additional seepage inputs from the surrounding slopes, which failed to have an impact during summer. An understanding of the complex interplay of antecedent soil moisture and the dynamics of subsurface seepage pathways in relation to the three‐dimensional distribution of sources is important in modelling heavy metal fluxes and levels in contaminated urban catchments. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   

15.
Biosorption potential of Cedrus deodara sawdust (CDS) in terms of sorption of Zn(II) ion across liquid phase has been evaluated in the present investigation. The surface of the CDS biomass before the sorption of Zn(II) ions seemed to be more porous, non‐crystalline and heterogeneous. The maximum uptake capacity of CDS was 97.39 mg g?1. Sorption of Zn(II) ion on the surface of CDS sawdust was maximum at pH 5, temperature 45°C, initial concentration of Zn(II) ion 100 mg L?1, biomass dose 1 g L?1, contact time 150 min, and agitation rate 160 rpm. Pseudo second‐order kinetics with the highest linear regression coefficient (R2 = 0.99), and lowest values of error functions, i.e., chi (χ2) and sum of square errors (SSE) against pseudo first‐order rate kinetics showed that the sorption of Zn(II) ion on the surface of CDS was mediated by chemosoprtive forces of attraction rather than physical adsorption. Mechanistically, relatively higher proportion of sorption of Zn(II) ion in early phase of contact time was profoundly explained by Bangham's equation and film diffusivity (Df). Intraparticle or pore diffusion (Dp) of Zn(II) ion inside the pores of CDS was rate limiting step at the later stage of contact time. Furthermore, the thermodynamic study on sorption of metal ion delineated the fact that the Zn(II) sorption on the surface of CDS was spontaneous, endothermic together with increased entropy at solid liquid interface.  相似文献   

16.
In this study, a modified method was used to increase the adsorption of lead ions from aqueous solutions by using modified clay mineral on the laboratory scale. Adsorption experiments have been carried out on the use of both thermal activated sepiolite (TAS) and their glutamate/sepiolite modification (GS) as adsorbents. The experimental data was analyzed using adsorption kinetic models (pseudo first‐ and second‐order equations). The pseudo second‐order kinetic model fitted well to the kinetic data (R2 ≥ 0.99). Then, the Freundlich and Langmuir models were applied to describe the uptake of Pb(II) on GS and the Langmuir isotherm model agrees well with the equilibrium experimental data (R2 ≥ 0.97). The maximum adsorption capacity was observed to be 128.205 mg/g by GS according to the Langmuir equation. Desorption efficiency of the GS was studied by the batch method using EDTA, HCl, and HNO3 solutions. Desorption of 69.18, 74.55, and 80% of Pb(II) from GS was achieved with 0.1 M EDTA, 0.1 M HCl, and 0.1 M HNO3 solutions, respectively. FTIR analysis suggests the importance of functional groups such as amino, hydroxyl, and carboxyl during Pb(II) removal. SEM observations demonstrated that an important interaction at the lead‐modified sepiolite interface occurred during the adsorption process. In addition, the thermodynamic constants was calculated that the values of the Gibbs free energy (ΔG*), enthalpy (ΔH*), and entropy (ΔS*) of modification were 86.79 kJ/mol, ?18.91 kJ/mol, and ?354.70 J/mol/K, respectively. The negative value of ΔH* shows exothermic nature of adsorption.  相似文献   

17.
Sorptive removal of Ni(II) from electroplating rinse wastewaters by cation exchange resin Dueolite C 20 was investigated at the temperature of 30°C under dynamic conditions in a packed bed. The effects of sorbent bed length 0.1–0.2 m, fixed flow rate 6 dm3 min?1, and the initial rinse water concentration (C0) 53.1 mg L?1 on the sorption characteristics of Dueolite C 20 were investigated at an influent pH of 6.5. More than 94.5% of Ni(II) was removed in the column experiments. The column performance was improved with increasing bed height and decreasing the flow rate. The Thomas, Yoon–Nelson, Clark, and Wolborska models were applied to the experimental data to represent the breakthrough curves and determine the characteristic design parameters of the column. The sorption performance of the Ni(II) ions through columns could be well described by the Thomas, Yoon–Nelson, and Wolborska models at effluent‐to‐influent concentration ratios (C/C0) >0.03 and <0.99. Among the all models, the Clark model showed the least average percentage time deviation. The sorptive capacity of electroplating rinse water using Ni(II) was found to be 45.98 mg g?1.  相似文献   

18.
210Pb- and137Cs-measurements, and varve counting have been used to date sediment cores from Lake Zurich (Switzerland). Two cores from different water depths were dated with210Pb/210Po and revealed sediment accumulation rates of (0.055±0.015) g·cm?2·y?1 and (0.09±0.03) g·cm?2·y?1, respectively. A comparable rate of (0.07±0.01) g·cm?2·y?1 has been obtained from137Cs measurements. These rates were confirmed by annual layer (varve)-counts which lead to rates of 0.07 g·cm?2·y?1. Constant210Pb activities were observed in the top 6 cm of the sediment cores. This constancy is generally explained in the literature by mixing processes caused by bioturbation and by distortion during coring operations of the uppermost water-rich fluffy sediments. However the distinct137Cs-maxima and the regular and undisturbed varve lamination of the top sediment observed in the cores of Lake Zurich contradict this assumption. In addition, measurements of7Be at the water/sediment interaces proved complete sediment core recovery and mechanically undisturbed sediments. Remobilization processes are assumed to cause the observed constant210Pb activities. Remobilization may also be the reason for an incomplete210Pb inventory in the sediments which contain only about 50% of the fallout from atmosphere. The results of the210Pb dating should therefore be considered with some care. If existent, varve counting represents the easiest and most reliable means for dating lake sediments.  相似文献   

19.
In India, the annual production of tea is ca. 857,000 tonnes, which is 27.4% of the total world production. The amount of tea factory waste (TFW) produced per annum after processing is ca. 190,400 tonnes. TFW can be used as a low cost adsorbent for the removal of toxic metals from the aqueous phase. An investigation was carried out to study the feasibility of the use of TFW as an adsorbent for the removal of the heavy metal, zinc. Equilibrium, kinetic and thermodynamic studies were reported. The straight line plot of log (qeq) versus time t for the adsorption of zinc shows the validity of the Lagergren equation. The various steps involved in adsorbate transport from the solution to the surface of the adsorbent particles were dealt with by using a Weber‐Morris plot, qe versus t0.5 for the TFW. The rate controlling parameters, kid,1 and kid,2, were determined and it was found that the macro‐pore diffusion rate was much larger than micro‐pore diffusion rate. A batch sorption model, which assumes the pseudo‐second‐order mechanism, was used to predict the rate constant of sorption, the equilibrium sorption capacity and the initial sorption rate with the effect of initial zinc (II) ion concentration. Equilibrium data obtained from the experiments were analyzed with various isotherms, i. e., Freundlich, Langmuir, Redlich‐Peterson and Tempkin. The adsorption equilibrium was reached in 30 min and the adsorption data fitted well to all models. The maximum adsorption capacity of TFW for zinc (II) ions was determined to be 14.2 mg/g. The capacity of adsorption on Zn(II) increased with increasing temperatures and pH. The maximum uptake level of zinc was observed at pH of 4.2. The various thermodynamic parameters, i. e., ΔG°, ΔH° and ΔS°, were estimated. The thermodynamics of the zinc ion/TFW system indicated a spontaneous, endothermic and random nature of the process. The results showed that the TFW, which has low economical value, is a suitable adsorbent for the removal of zinc (II) ions from aqueous solutions.  相似文献   

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