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1.
Adsorption kinetic and equilibrium studies of two reactive dyes, namely, Reactive Red 31 and Reactive Red 2 were conducted. The equilibrium studies were conducted for various operational parameters such as initial dye concentration, pH, agitation speed, adsorbent dosage and temperature. The initial dye concentration was varied from 10 - 60 mg/L, pH from 2–11, agitation speed from 100–140 rpm, adsorbent dosage from 0.5 g to 2.5 g and temperature from 30 °C -50 °C respectively. The activated carbon of particle size 600 μm was developed from preliminary tannery sludge. The dye removal capacity of the two reactive red dyes decreased with increasing pH. The zero point charge for the sludge carbon was 9.0 and 7.0 for the two dyes, respectively. Batch kinetic data investigations on the removal of reactive dyes using tannery sludge activated carbon have been well described by the lagergren plots. It was suggested that the Pseudo second order adsorption mechanism was predominant for the sorption of the reactive dyes onto the tannery sludge based carbon. Thus, the adsorption phenomenon was suggested as a chemical process. The adsorption data fitted well with Langmuir model than the Freundlich model. The maximum adsorption capacity(q0) from Langmuir isotherm were found to have increased in the range of 23.15–39.37 mg/g and 47.62–55.87 mg/g for reactive dyes reactive red 31 and reactive red 2, respectively.  相似文献   

2.
Removal of chromate from drinking water using powder carbon steel   总被引：2，自引：0，他引：2  
This paper presents the possible alternative removal options for the development of safe drinking water supplies in areas affected by hexavalent chromium. Chromate is a matter of great environmental concern due to its extensive contamination and carcinogenic toxicity. In this study, the conventional adsorption with various types of adsorbent method were used for chromate removal, but only powder carbon steel was compatible with household water treatment and can be designated based on high removal efficiency and affordable cost. Home powder carbon steel with granular activated carbon (PCS–GAC) treatment systems are quite simple. Water needing treatment passes through the cartridge or filter candles contacting PCS–GAC on its way to the faucet. This method is based on the use of powder carbon steel, ML 90 Bombril S.A, as a cleaning agent. Granular activated carbon filters have been employed in home water purification systems essentially for the removal of taste, odor, and color. The effect of pH, redox potential, time, and adsorbate concentration on the uptake carbon steel were observed. The lack of desorption suggests that anion chromium is irreversibly sorbed by the powder carbon steel.  相似文献   

3.
A zinc oxide-coated nanoporous carbon sorbent was prepared by acid modification and ZnO functionalization of mesoporous carbon. The synthesized materials, such as mesoporous carbon, oxidized mesoporous carbon and zinc oxide-coated nanoporous carbon, were characterized by nitrogen adsorption–desorption analysis, Fourier transform infrared spectra, scanning electron microscopy, and transmission electron microscopy. ZnO on oxidized mesoporous carbon gradually increased with increase in the number of cycles. Furthermore, the effects of agitation time, initial metal ions concentration, adsorbent dose, temperature and pH on the efficiency of Pb(II) ion removal were investigated as the controllable factors by Taguchi method. The value of correlation coefficients showed that the equilibrium data fitted well to the Langmuir isotherm. Among the adsorbents, zinc oxide-coated nanoporous carbon showed the largest adsorption capacity of 522.8 mg/g (2.52 mmol/g) which was almost close to that of the zinc oxide-coated (2.38 mmol/g), indicating the monolayer spreading of ZnO onto the oxidized mesoporous carbon. The results of the present study suggest that ZnO-coated nanoporous carbon can be effectively used for Pb(II) adsorption from aqueous solution, whereas a part of acidic functional groups may be contributed to binding the Pb(II) for the oxidized mesoporous carbon and mesoporous carbon. Kinetic studies indicated that the overall adsorption process of Pb(II) followed the pseudo-second-order model. The ZnO-coated nanoporous carbon was regenerated and found to be suitable of reuse of the adsorbent for successive adsorption–desorption cycles without considerable loss of adsorption capacity.  相似文献   

4.
Batch sorption system using co-immobilized (activated carbon and Bacillus subtilis) beads as adsorbent was investigated to remove Cr(VI) from aqueous solution. Fourier transform infrared spectroscopy analysis showed the functional groups of both bacteria and activated carbon in co-immobilized beads. Experiments were carried out as a function of contact time (5–300 min), initial metal concentration (50–200 mg L?1), pH (2–8), and adsorbent dose (0.2–1 g L?1). The maximum percentage of removal was found to be 99 %. Langmuir model showed satisfactory fit to the equilibrium adsorption data of co-immobilized beads. The kinetics of the adsorption followed pseudo-second-order rate expression, which demonstrates that chemisorption plays a significant role in the adsorption mechanism. The significant shift in the Fourier transform infrared spectroscopy peaks and a Cr peak in the scanning electron microscope–energy dispersive spectroscopy spectra further confirmed the adsorption. The results indicate that co-immobilized beads can be used as an effective adsorbent for the removal of Cr(VI) from the aqueous solution.  相似文献   

5.
In this study, the adsorption behavior of Ni(II) in an aqueous solution system using natural adsorbent Peganum harmala-L was measured via batch mode. The prepared sorbent was characterized by scanning electron microscope, Fourier transform infrared spectroscopy, N2 adsorption–desorption and pHzpc. Adsorption experiments were carried out by varying several conditions such as contact time, metal ion concentration and pH to assess kinetic and equilibrium parameters. The equilibrium data were analyzed based on the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherms. Kinetic data were analyzed using the pseudo-first-order, pseudo-second-order and intra-particular diffusion models. Experimental data showed that at contact time 60 min, metal ion concentration 50 mg/L and pH 6, a maximum amount of Ni(II) ions can be removed. The experimental data were best described by the Langmuir isotherm model as is evident from the high R 2 value of 0.988. The adsorption capacity (q m) obtained was 68.02 mg/g at an initial pH of 6 and a temperature of 25 °C. Kinetic studies of the adsorption showed that equilibrium was reached within 60 min of contact and the adsorption process followed the pseudo-first-order model. The obtained results show that P. harmala-L can be used as an effective and a natural low-cost adsorbent for the removal of Ni(II) from aqueous solutions.  相似文献   

6.
The batch removal of hexavalent chromium from aqueous solutions using almond shell, activated sawdust, and activated carbon, which are low-cost biological wastes under different experimental conditions, was investigated in this study. The influences of initial concentration, adsorbent dose, adsorbent particle size, agitation speed, temperature, contact time, and pH of solution were investigated. The adsorption was solution pH dependent and the maximum adsorption was observed at a solution pH of 2.0. The capacity of chromium adsorption under equilibrium conditions increased with the decrease in particle sizes. The equilibrium was achieved for chromium ion after 30?min. Experimental results showed that low-cost biosorbents are effective for the removal of pollutants from aqueous solution. The pseudo-second-order kinetic model gave a better fit of the experimental data as compared to the pseudo-first-order kinetic model. Experimental data showed a good fit with the Freundlich isotherm model. Changes in the thermodynamic parameters, including Gibbs free energy (??Go), enthalpy (??Ho), and entropy (??So), indicated that the biosorption of hexavalent chromium onto almond shell, activated sawdust, and activated carbon was feasible, spontaneous, and endothermic in the temperature range 28?C50?°C.  相似文献   

7.
以高比表面积活性炭作为吸附剂制备电容电极,研究电容去离子化（CDI）对地下水中镉的吸附性能。分别探讨了镉初始质量浓度、体系供电电压、地下水中常见阳离子种类对CDI去除镉的影响。结果表明,CDI吸附镉符合准二级吸附动力学、满足Langmuir等温吸附方程,CDI对镉的吸附为单分子层吸附。吸附量随镉初始质量浓度的升高而增加;在低质量浓度时,较高的供电电压会提高初始阶段的吸附速率,但对电极的最终吸附量无显著影响;地下水中主要阳离子的存在增加了体系的电导率,从而促进了CDI对镉的吸附,提高了镉的吸附速率和去除率。  相似文献   

8.
北方典型内陆盆地高砷地下水的水化学特征及处理技术   总被引：1，自引：0，他引：1  
赵凯  郭华明  高存荣 《现代地质》2015,29(2):351-360
我国高砷地下水分布广泛,是受砷污染最严重的地区之一,严重危害居民身体健康,开发经济、高效、环境友好的高砷地下水修复治理技术极具必要性。以大同盆地、呼包平原、河套平原和银川平原为代表性研究区域,归纳总结了北方干旱、半干旱地区典型高砷地下水区水化学特征。通常情况下,高砷地下水的pH值较高,共存阴离子(HCO-3、SO2-4和Cl-)浓度较大,溶解性有机碳含量较高,并且As(Ⅲ)为主要砷形态。开展了针对北方典型高砷地下水特定水化学环境特点(如pH值、共存阴阳离子以及溶解性有机物等)的改性天然菱铁矿除砷性能研究。结果表明,改性天然菱铁矿对溶液pH值具有良好的缓冲能力,其除砷性能基本不受pH值、共存阴离子、Ca/Mg阳离子及以腐殖酸为代表的溶解性有机物等典型高砷地下水水化学特征因素的影响,表明吸附剂对砷具有良好的吸附选择性。另外,改性天然菱铁矿对As(Ⅲ)的去除效果优于对As(V)的去除效果,因此,利用改性天然菱铁矿作为反应介质材料,将其应用于处理主要以As(Ⅲ)形式存在的高砷地下水具备良好的发展前景。  相似文献   

9.
The carbon–alumina composite pellet was developed for the adsorption of acid fuchsin from its aqueous solution. The composite pellet was characterized using Brunauer–Emmett–Teller method, scanning Electron Microscopy and Fourier Transform Infrared Spectroscopy. The adsorption capacity of commercial alumina, commercial activated carbon and the prepared composite pellet was investigated against acid fuchsin, and the adsorption capacity was found to be increased in the order of alumina < carbon–alumina composite pellet < activated carbon. Although the adsorption capacity of carbon–alumina composite pellets was less than that of activated carbon, the use of the pelletized form of the present adsorbent was proven to be advantageous for the use in the packed-bed column. The experimental data were fitted to Langmuir, Freundlich and Temkin adsorption isotherms, and the equilibrium behavior was well explained by Langmuir isotherm. Besides, the kinetic behavior was well predicted by pseudo-second-order kinetics. The effects of inlet dye concentration (10–20 mg/L), feed flowrate (5–15 mL/min) and bed height (2.54–7.62 cm) on the breakthrough characteristics were investigated using a fixed-bed column. The maximum removal capacity in the column study was found to be 343.87 mg/L with an initial dye concentration and flowrate of 20 and 10 mL/min according to Bohart–Adams model. The breakthrough behavior was also effectively described by the Yoon–Nelson and Clark models.  相似文献   

10.
为揭示旱地和水田土壤镉的吸附解吸特征,以江汉平原黄豆地、棉花地以及水稻田土壤为研究对象,开展土壤镉的吸附动力学实验、等温吸附?解吸实验以及有机质的影响实验.结果表明:江汉平原土壤对镉的吸附是一个较为复杂的吸附动力学过程且以化学吸附为主,研究区土壤镉的初始吸附速率总体上表现为水田土壤大于旱地土壤;旱地土壤对Cd2+具有较...  相似文献   

11.
In the present experimental study, solid waste was used as an adsorbent and the effectiveness of the adsorbent was increased by novel treatment methods. Red mud, acid-treated activated red mud and iron oxide-coated acid-treated activated red mud were used for the removal of lead (II). The structural and functional groups were identified to confirm the removal of lead (II) by powder X-ray diffraction and Fourier transform infrared spectroscopy analyses. The enhancement of surface area was confirmed by Brunauer–Emmett–Teller analysis. Batch adsorption experiment was also conducted, and various parameters such as the effect of adsorbent dosage, pH, contact time and initial ion concentration were analyzed and reported. Adsorption equilibrium data were investigated using Langmuir, Freundlich and Dubinin–Radushkevich isotherm models with three parameters, and the rate of reaction was examined through kinetic models. The results indicate that in particular a novel modified form of red mud, namely iron oxide-coated acid-treated activated red mud was well fitted in lead (II) removal compared with reported adsorbents. The Langmuir isotherm shows that the maximum adsorption of adsorbate per gram was greater than other adsorbents (27.02 mg/g). In Freundlich isotherm, the Freundlich constant n values lie between 1 and 10 indicate the favorable adsorption. The calculated n values for normal red mud, acid-treated activated red mud and iron oxide-coated acid-treated activated red mud were found to be 1.9, 2.1 and 2.0 respectively. The correlation coefficient value was higher and the rate of reaction follows the pseudo-second-order kinetic model.  相似文献   

12.
Zeolites are known to possess valuable physiochemical properties such as adsorption, cation exchange, molecular sieving, and catalysis. In addition, zeolites are highly selective scavengers of a variety of heavy metals from liquid effluents through the process of ion exchange. The present study was performed to hydrothermally synthesize Na8[AlSiO4]6(OH)2·2H2O (also known as hydroxy sodalite hydrate). Due to its small aperture size, this material can be an ideal candidate for the separation of small molecules and ions from aquatic and gas mixtures. Synthetic zeolites offer many advantages over natural zeolites, such as higher ion affinity and adsorption capacity. Batch adsorption isotherm studies were conducted to evaluate the obtained adsorbent for the lead ion removal from aqueous media. Modeling lead ion adsorption using Langmuir and Freundlich isotherm expressions determined the capacity of the adsorbent. A removal efficiency of 98.1 % in a 3.0 g/l adsorbent/solution mixture with a maximum adsorption capacity of 153.8 mg/g was obtained. One potential application of the synthesized zeolite is for the lead removal in point-of-use treatment devices.  相似文献   

13.
The adsorption behavior study of diethyl and dibutyl phthalates was investigated onto a new activated carbon prepared from an abundant biomass “Albizia julibrissin pods,” treated chemically by H3PO4. A series of experiments were conducted in a batch system to estimate the effect of operating conditions such as the adsorbent nature, the dose of adsorbent, the contact time, the initial concentration and the temperature on the adsorption efficiency. The optimum operating conditions were found to be 0.1 and 0.05 g of adsorbent for diethyl and dibutyl phthalates, respectively, at 30 min equilibrium time, 150 mg g?1 and 293 K. The adsorption isotherms for both phthalates were fit at different temperatures using the nonlinear regression of Langmuir, Freundlich, Dubinin–Radushkevich and Redlich–Peterson. The pseudo-first order, pseudo-second order by nonlinear regression and intraparticle diffusion models were used to describe the adsorption kinetic. The results show that the intraparticle diffusion model is not the limiting step governing the adsorption mechanism. The structural and textural characteristics of adsorbent surface were investigated. FTIR analysis of unloaded and phthalates-loaded adsorbent revealed that the aliphatic groups attached to phthalate esters are involved in adsorption mechanism.  相似文献   

14.
Numerous studies of marine environments show that dissolved organic carbon (DOC) concentrations in sediments are typically tenfold higher than in the overlying water. Large concentration gradients near the sediment–water interface suggest that there may be a significant flux of organic carbon from sediments to the water column. Furthermore, accumulation of DOC in the porewater may influence the burial and preservation of organic matter by promoting geopolymerization and/or adsorption reactions. We measured DOC concentration profiles (for porewater collected by centrifugation and “sipping”) and benthic fluxes (with in situ and shipboard chambers) at two sites on the North Carolina continental slope to better understand the controls on porewater DOC concentrations and quantify sediment–water exchange rates. We also measured a suite of sediment properties (e.g., sediment accumulation and bioturbation rates, organic carbon content, and mineral surface area) that allow us to examine the relationship between porewater DOC concentrations and organic carbon preservation. Sediment depth-distributions of DOC from a downslope transect (300–1000 m water depth) follow a trend consistent with other porewater constituents (ΣCO2 and SO42−) and a tracer of modern, fine-grained sediment (fallout Pu), suggesting that DOC levels are regulated by organic matter remineralization. However, remineralization rates appear to be relatively uniform across the sediment transect. A simple diagenetic model illustrates that variations in DOC profiles at this site may be due to differences in the depth of the active remineralization zone, which in turn is largely controlled by the intensity of bioturbation. Comparison of porewater DOC concentrations, organic carbon burial efficiency, and organic matter sorption suggest that DOC levels are not a major factor in promoting organic matter preservation or loading on grain surfaces. The DOC benthic fluxes are difficult to detect, but suggest that only 2% of the dissolved organic carbon escapes remineralization in the sediments by transport across the sediment-water interface.  相似文献   

15.
At present, there is growing interest in using low cost, commercially available materials for the adsorption of heavy metals. The major advantages of adsorption technologies are its effectiveness in reducing the concentration of heavy metal ions to very low levels and the use of inexpensive adsorbent materials. In this review, agricultural and forest waste adsorbents were used to remove Pb2+ ions in wastewater treatment, and their technical feasibilities were reviewed in studies mainly from 2000 to 2010. They all were compared with each other by metal binding capacities, metal removal performances, sorbent dose, optimum pH, temperature, initial concentration and contact time. Although commercial activated carbon is widely used in wastewater treatment applications, it has high costs. The use of agricultural by-products as adsorbent material to purify heavy metal contaminated water has become increasingly popular through the past decade because they are less expensive, biodegradable, abundant and efficient. Instead of activated carbon, this study was focused on the inexpensive materials such as agricultural and forest waste. It was shown that these alternative adsorbents had sufficient binding capacity to remove Pb2+ ions from wastewater.  相似文献   

16.
Vitis vinifera (grape) leaf litter, an abundant agricultural waste in South Africa was chemically modified with H3PO4 and carbonized for use as biosorbent. Characterization and the potential application of the adsorbent in simultaneous removal of 4-nitrophenol and 2-nitrophenol from aqueous solutions were investigated. The adsorbent was characterized using FTIR, SEM and EDX elemental microanalysis. The EDX and FTIR analysis revealed the presence of surface oxygen moieties capable of binding to adsorbate molecules while the SEM micrographs showed the development of pores and cavities in the adsorbent. Batch adsorption experiments were conducted at a varying contact time, adsorbent dosage, pH and initial adsorbate concentration to investigate optimal conditions. The maximum adsorption capacity of the adsorbent was 103.09 and 103.10 mg/g for 4-nitrophenol and 2-nitrophenol, respectively. The adsorption process was best fitted into Freundlich isotherm while the adsorption kinetics followed a pseudo-second-order model. Liquid film and intra-particle diffusion contributed to the adsorption process. Thermodynamic parameters of ΔG°, ΔH° and ΔS° were evaluated. The adsorption was exothermic, feasible and spontaneous. The results suggest a possible application of grape leaf litter as a precursor for activated carbon and for cheaper wastewater treatment technologies.  相似文献   

17.
The extensive use of Rhodamine B (RhB) for textile, paper, pigment, food, cosmetic, and drug manufacturing and its indiscriminate disposal leads to serious human, biological, and environmental hazards. A magnetic adsorbent with silicate and phenyl polymers (Ph/SiO2/Fe3O4) has been prepared to absorb RhB. The morphology and structure of the adsorbents have been characterized by TGA, XRD, FTIR, and adsorption–desorption measurement. The results revealed that Ph/SiO2/Fe3O4 exhibited a paramagnetic behavior and could easily and quickly be separated from a suspension. The RhB adsorption behavior was almost pH independent due to the adsorption between the phenyl ring of Ph/SiO2/Fe3O4 and RhB by π–π electron-donor–acceptor interactions. The adsorption behavior of RhB adsorption was in good agreement with the Langmuir adsorption isotherm, and the maximum adsorption capacity was 142.186 mg g?1. Good desorption performance of Ph/SiO2/Fe3O4 showed that this novel magnetic adsorbent cannot only be activated by ethanol extraction process but also reuse by the recovery of magnetic force.  相似文献   

18.
The effects of varying operating conditions on metals removal from aqueous solution using a novel nano-size composite adsorbent are reported in this paper. Characterization of the composite adsorbent material showed successful production of carbon nanotubes on granular activated carbon using 1 % nickel as catalyst. In the laboratory adsorption experiment, initial mixed metals concentration of 2.0 mg/L Cu2+, 1.5 mg/L Pb2+ and 0.8 mg/L Ni2+ were synthesized based on metals concentration from samples collected from a semiconductor industry effluent. The effects of operation conditions on metals removal using composite adsorbent were investigated. Experimental conditions resulting in optimal metals adsorption were observed at pH 5, 1 g/L dosage and 60 min contact time. It was noted that the percentage of metals removal at the equilibrium condition varied for each metal, with lead recording 99 %, copper 61 % and nickel 20 %, giving metal affinity trend of Pb2+ > Cu2+ > Ni2+ on the adsorbent. Langmuir’s adsorption isotherm model gave a higher R2 value of 0.93, 0.89 and 0.986 for copper, nickel and lead, respectively, over that of Freundlich model during the adsorption process of the three metals in matrix solution.  相似文献   

19.
Microwave-assisted tetrabutyl ammonium-impregnated sulphate-crosslinked chitosan was synthesized for enhanced adsorption of hexavalent chromium. The adsorbent obtained was extensively characterized using Fourier transform infrared, X-ray diffraction, scanning electron microscopy and energy-dispersive X-ray studies. Various isotherm models such as Langmuir, Freundlich and Dubinin–Radushkevich were studied to comprehend the adsorption mechanism of hexavalent chromium by the adsorbent. Maximum adsorption capacity of 225.9 mg g?1 was observed at pH 3.0 in accordance with Langmuir isotherm model. The sorption kinetics and thermodynamic studies revealed that adsorption of hexavalent chromium followed pseudo-second-order kinetics with exothermic and spontaneous behaviour. A column packed with 1 g of adsorbent was found to give complete adsorption of Cr(VI) up to 900 mL of 200 mg L?1 solution which discerns the applicability of the adsorbent material for higher sample volumes in column studies. The effective adsorption results were obtained due to both ion exchange and ion pair interaction of adsorbent with hexavalent chromium. Greener aspect of overall adsorption was regeneration of the adsorbent which was carried out using sodium hydroxide solution. In the present study, the regenerated adsorbent was effectively reused up to ten adsorption–desorption cycles with no loss in adsorption efficiency.  相似文献   

20.
This work aimed to investigate the adsorption characteristics, both kinetically and thermodynamically, of Cu(II) and Pb(II) removal from aqueous solutions onto mixed-waste activated carbon, as well as to study the competitive behavior found in mixed heavy metal solution systems. This study shows that activated carbon prepared from mixed waste is an effective adsorbent for the removal of Cu(II) and Pb(II) from aqueous solutions, with the aim of detoxifying industrial effluents before their safe disposal onto water surfaces. The adsorption process was characterized in terms of kinetic and thermodynamic studies. In addition, the influence of presence of Cu(II) and Pb(II) in a competitive system was investigated. The results showed that the maximum adsorption capacities were gained at a pH of 6 with a contact time of 180 min, a metal solution concentration of 300 ppm, and an adsorbent dose of 0.3 g/L. The adsorption process was found to follow a pseudo-first-order kinetic model. Thermodynamic parameters such as ΔG o, ΔH o, and ΔS o showed that the sorption process was spontaneous and endothermic in nature. A competitive study demonstrated the applicability of mixed-waste activated carbon to adsorb Cu(II) and Pb(II) from a solution of mixed metals. In addition, the adsorption capacity was found to be as effective as other adsorbents reported in the literature. The developed adsorptive removal procedure was applied for treatment of real wastewater samples and showed high removal efficiency.  相似文献   

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