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1.
Clays, particularly kaolinite, are promising adsorbents for the treatment of textile effluents, but there is a need of better understanding the mechanisms of adsorption, especially in the case of anionic dyes. Thus, the removal of RR120 anionic dye was investigated using Tunisian raw clay (TBK) composed of kaolinite and illite, and a standard kaolinite (KGa-2), and conducting batch experiments by varying different parameters (contact time, ionic strength, concentration, temperature). We investigated the clays’ surface charges by electrophoretic mobility measures and the dye-clay interactions during adsorption, by the streaming-induced potentials (SIP). The results showed that KGa-2 has higher adsorption capacity for RR120 dye than TBK clay, moreover enhanced by increasing the ionic strength and/or lowering the pH of the aqueous. The SIP results showed an increase of negative charges for both clays, reflecting the adsorption of the anionic dye on the positive charges of the amphoteric surfaces of the clays. The SIP magnitudes indicated a higher adsorption rate for KGa-2 in accordance with the kinetic study. The Sips model that described the best adsorption isotherms indicates lateral interactions of the dye molecules, stronger in the case of KGa-2 than TBK. Also, the dye molecules form a thinner layer on KGa-2 surfaces. In addition, the dye molecule’s structure was not altered, as verified by mass spectrometry. The adsorption process was feasible and spontaneous and favored at ambient temperature. Thus, kaolinite-rich clays are effective in the removal of anionic dyes in aqueous solution and potential good adsorbents in wastewater treatment.  相似文献   

2.
The present work investigated the adsorption and mobility (desorption) of Sb(V) on kaolinite using batch experiments. The adsorption of Sb(V) on kaolinite was studied as a function of contact time, pH, ionic strength, humic acid (HA), initial Sb(V) concentration and temperature. Kinetic studies suggest that the equilibrium is achieved within 24 h. The adsorption of Sb(V) was strongly affected by changes in I at low ionic strength and unaffected at high ionic strength. The adsorption is weakly dependent on the presence of humic acid, but is strongly dependent on pH. Within the range tested, the optimal pH for Sb(V) adsorption is 3.6, and close to 75% removal can be achieved. Desorption is dependent on the original suspension pH. The addition sequence of Sb(V)/HA do not influence the adsorption of Sb(V) on kaolinite. The adsorption data fit both the Freundlich and Langmuir isotherm. The thermodynamic parameters (ΔH 0, ΔS 0 and ΔG 0) were calculated from the temperature dependence, and the results suggest the endothermic and spontaneous nature of the process.  相似文献   

3.
In the present study, Juglans regia shells were used to prepare activated carbon by acid treatment method. J. regia shell-based activated carbon was used for the adsorption of two synthetic dyes namely, a basic dye malachite green and an acid dye amido black 10B. The prepared adsorbent was crushed and sieved to three different mesh sizes 100, 600 and 1,000 μm. The adsorbent was characterized by scanning electron microscopy, surface acidity and zero-point charge. Batch experiments were carried out by varying the parameters like initial aqueous phase pH, adsorbent dosage and initial dye concentration. The equilibrium data were tested with Langmuir, Freundlich, Redlich–Peterson and Sips isotherm at three different temperatures 293, 300 and 313 K and it was found that the Freundlich isotherm best fitted the adsorption of both the dyes. Kinetic data were tested with pseudo first-order model and pseudo second-order model. The mechanism for the adsorption of both the dyes onto the adsorbent was studied by fitting the kinetic data with intraparticle diffusion model and Boyd plot. External mass transfer was found to be the rate-determining step. Based on the ionic nature of the adsorbates, the extent of film diffusion and intraparticle diffusion varied; both being system specific. Thermodynamic parameters were also calculated. Finally, the process parameters of each adsorption system were compared to develop the understanding of the best suitable system.  相似文献   

4.
Atomic layer deposition (ALD) thin film coating was applied to improve the hydrophilia of biochar derived from black willow. 2 (2Al, 0.82 wt% Al2O3), 5 (5Al, 1.40 wt% Al2O3), and 10 (10Al, 2.36 wt% Al2O3) cycles of alumina ALD were applied. The biochars were characterized by inductively coupled plasma–atomic emission spectroscopy, nitrogen adsorption and desorption, scanning electron microscopy, and Fourier transform infrared spectroscopy. The adsorbents were utilized for the removal of methylene blue (MB) from an aqueous solution to evaluate their adsorption capacities. The 5Al biochar showed the highest adsorption capacity, compared to the uncoated biochar and other Al2O3 coated biochars, due to its improved hydrophilia. The amount of MB adsorbed onto the 5Al biochar was almost three times that adsorbed onto the uncoated biochar during the first hour of adsorption experiments. Adsorption isotherms were modeled with the Langmuir and Freundlich isotherms. The data fit well with the Langmuir isotherm, and the maximum adsorption capacities were found to be 26.8 and 35.0 mg/g at 25 °C for the uncoated biochar and 5Al biochar, respectively. The adsorbed MB amount per square meter achieved 1.3 mg/m2 onto the 5Al biochar, and it was twice the amount on the uncoated biochar. The experimental data were analyzed by pseudo-first-order and pseudo-second-order kinetics models of adsorption. The pseudo-second-order model better describes adsorption kinetic data for the uncoated biochar and 5Al biochar than the pseudo-first-order model does.  相似文献   

5.
作为典型的黑炭,近年来生物炭的应用发展受到人们广泛关注。由于生物炭施加在土壤中,在表生地球化学长期作用下,会有部分逐渐破碎变小,直至微米、纳米级别,在土壤或水体中迁移,因此,对生物炭、特别是活性更强的纳米级生物炭的迁移性研究具有十分重要的意义,而关于纳米级生物炭的迁移性研究目前十分匮乏。通过石英砂柱中纳米生物炭的柱迁移实验,获得天然有机质和不同pH值(4、7、10)条件下的穿透曲线和空间滞留曲线,研究影响作用机制。结果表明：天然有机质(腐殖酸)能增强纳米生物炭的迁移性,中碱性pH环境也有助于其迁移。一方面纳米炭的分散性得到改善,另一方面腐殖酸和碱性环境有助于增加纳米炭和石英砂介质的颗粒表面负电荷,增大Zeta电位值(负值),从而使颗粒间静电排斥力增强,有助于纳米炭的迁移。研究结果对深入理解生物炭在自然界中地球化学迁移行为及其吸附污染物后的潜在迁移风险具有重要意义。  相似文献   

6.
Adsorption of bisphenol A on a lignin isolated from black liquor, a waste product of the paper industry, was investigated to assess the possibility of using the lignin to remove bisphenol A from waters. Effects of pH, ionic strength, heavy metals, and dissolved organic matter (DOM) on adsorption were examined. Adsorption equilibrium was approached within 5?h. The adsorption capacity of bisphenol A on lignin was as high as 237.07?mg/g. Ionic strength had no influence on the adsorption, while higher pH above 7.5 inhibited bisphenol A adsorption due to the repulsive electrostatic interaction between bisphenolate anion and the negatively charged lignin surface. The presence of heavy metals of copper and lead increased the adsorption by 11.90 and 26.80?%, respectively, possibly through modifying the physiochemical configuration characteristics of labile fraction of the lignin and reducing the polarity of it. No obvious impact of DOM on the adsorption was observed. The results of this study suggest that lignin is a promising adsorbent material to remove bisphenol A in wastewater containing complex components such as heavy metals and DOM, particularly at acid and neutral conditions.  相似文献   

7.
Vertical flow bioreactors (VFBR) are often used as a component of passive treatment systems (PTS) to treat mine drainage. One of the primary purposes of VFBR is to remove trace metals from mine drainage and retain them in the organic substrate. Elevated ionic strength may impact the performance of VFBR and affect their ability to remove trace metals. A paired-comparison study was performed to determine how products of trace metal removal may change when ionic strength is elevated due to increased concentrations of common contributors to TDS, specifically sodium and sulfate. A sequential extraction procedure (SEP) and acid-volatile sulfide/simultaneously extracted metals analyses (AVS/SEM) were used to determine dominant Cd, Mn, Ni, Pb, and Zn removal products in bench-scale VFBR. Elevated ionic strength resulted in more Pb being retained in the substrates as an insoluble sulfide and less Mn being removed via adsorption to the substrates. An increase in ionic strength had a greater impact on adsorption when sulfate reduction was inhibited, with percentages of Mn and Zn removed via this mechanism decreasing by at least half. This finding could be particularly significant at the start of VFBR operation when adsorption is expected to be the primary removal mechanism.  相似文献   

8.
Biochars have received increasing attention in recent years because of their significant properties such as carbon sequestration, soil fertility, and contaminant immobilization. In this work, the adsorptive removal of paraquat (1,1′-dimethyl-4,4′-dipyridinium chloride, one of the most widely used herbicides) from aqueous solution onto the swine-manure-derived biochar has been studied at 25 °C in a batch adsorption system. The adsorption rate has been investigated under the controlled process parameters including initial pH (i.e., 4.5, 6.0, 7.5, and 9.0), paraquat concentration (i.e., 0.5, 1.0, 2.0, 4.0, and 6.0 mg/L), and biochar dosage (i.e., 0.10, 0.15, 0.20, 0.25, and 0.30 g/L). Based on the adsorption affinity between cationic paraquat and carbon-like adsorbent, a pseudo-second order model has been developed using experimental data to predict the adsorption kinetic constant and equilibrium adsorption capacity. The results showed that the adsorption process could be satisfactorily described with the reaction model and were reasonably explained by assuming an adsorption mechanism in the ion exchange process. Overall, the results from this study demonstrated that the biomass-derived char can be used as a low-cost adsorbent for the removal of environmental cationic organic pollutants from the water environment.  相似文献   

9.
Tarap peel (TP) and oxalic-acid-modified Tarap peel (TP-OX) were used to remove brilliant green (BG) dye from aqueous solution. Surface modification of TP suggested that functional groups such as carboxyl, hydroxyl and amino were involved in the adsorption of BG onto TP. Parameters such as effects of pH, contact time, ionic strength, initial dye concentration and temperature were included to study the adsorption of BG onto TP and TP-OX. Adsorption isotherm models were used to investigate the adsorption process, while kinetics models were used to provide insight into the adsorption mechanisms. Optimised contact time of 2 h with no pH adjustment was used. Adsorption of BG onto TP was best fitted to the Freundlich model, while experimental data for TP-OX are best described by the Tempkin model. The maximum adsorption capacities were determined as 174 and 275 mg g?1 for TP and TP-OX, respectively. Thermodynamics study indicated the endothermic nature of adsorptions of BG onto both adsorbents. According to kinetics study, the adsorption mechanisms on both adsorbents followed pseudo-second-order model, and film diffusion might have major role in the adsorption process.  相似文献   

10.
Contamination of surface water and groundwater by organic pollutants is a serious problem due to their persistence, bioaccumulation and biomagnification through food webs. Since the removal of dyes from wastewater is considered an environmental challenge and government legislation requires textile wastewater to be treated, therefore there is a constant need to have an effective process that can efficiently remove these dyes. The aim of the present study is to evaluate the potentiality of dried Carpobrotus edulis plant as low-cost adsorbent for the removal of the industrial acid blue 113 dye from aqueous solutions using the batch equilibration technique. The effects of different physicochemical parameters such as adsorbent dose, contact time, initial dye concentration, solution pH and temperature on adsorption rate of anionic AB113 dye on microparticles of dried C. edulis plant were investigated. The experimental data were analyzed by using mathematical models to determine the thermodynamic parameters. The negative values of free energy change indicated the spontaneous nature of the adsorption and negative value of enthalpy change suggested the exothermic nature of the adsorption process. These results indicate that dried C. edulis plant as an environmentally friendly adsorbent could be potentially used for the removal of anionic dyes from aqueous solutions.  相似文献   

11.
In this work, clinoptilolite was modified with conducting polyaniline polymer and then the nanocomposite was used as an adsorbent for methyl orange (MO) as a model dye. Cations located in clinoptilolite structure like Na+, K+, Mg2+, Ca2+ were exchanged with anilinium cations and then the polymerization of anilinium cations in and outside of the clinoptilolite channels resulted in the formation of polyaniline/clinoptilolite nanocomposite. The resulted nanocomposite was used for the removal of MO from aqueous solution. The effect of various factors like contact time, concentration of dye as well as the amount of adsorbent on the removal efficiency of dye was investigated. The adsorption isotherms were investigated. It was found that the equilibrium adsorption data were well described by the Langmuir isotherm model. The kinetic studies indicated that the adsorption process was controlled by pseudo-second-order equation. High adsorption capacity and low contact time as well as the low cost of modified clinoptilolite proved that it is an efficient adsorbent for the removal of MO from aqueous solutions.  相似文献   

12.
天然黄铁矿对阳离子有机染料RhB吸附特性研究   总被引：1，自引：0，他引：1  
以黄铁矿作为吸附剂研究罗丹明B(Rhodamine B,RhB)的吸附特性,用X射线衍射仪(XRD)、扫描电子显微镜(SEM)对黄铁矿进行了表征。考察了接触时间、溶液pH值、离子强度、温度等对黄铁矿吸附RhB的影响。结果表明,在吸附平衡时间120 min、pH值4.0时,吸附量达到最大值21.3 mg/g。升高温度,黄铁矿对RhB的吸附量逐渐增大。而离子强度对吸附几乎没有影响。实验数据与Langmuir吸附模型拟合良好,整个吸附动力学模型符合准二级吸附动力学模型。热力学研究证实了该吸附过程是自发进行的。通过对吸附反应结束后的黄铁矿进行煅烧处理,去除表面吸附的RhB,结果表明煅烧一次的黄铁矿仍然可以吸附废水中约50%的RhB,具有重复利用的价值。  相似文献   

13.
为了对地下水系统中天然胶体与Ni2+的共迁移特征进行研究,通过静态吸附实验和石英砂模拟含水层介质柱实验研究了土壤胶体对Ni2+在地下水中运移的影响,以及pH、离子强度（IS）、有机质等对土壤胶体吸附Ni2+的影响。结果表明：随着pH值升高,土壤胶体对Ni2+的吸附量增加;离子强度的增加会显著地降低土壤胶体吸附Ni2+的能力;腐殖酸（HA）的存在会增强胶体对Ni2+的吸附能力;在有胶体的情况下,Ni2+穿透砂柱的时间会缩短,吸附能力增强,吸附量增加,但当离子强度增加时,虽然Ni2+穿透砂柱的时间也被缩短,但是吸附量却降低。  相似文献   

14.
This article presents the use of ionic liquid in the removal process of thallium ions using solid–liquid extraction by impregnating ionic liquid (1-n-hexyl-3-methylimidazolium chloride) onto an inorganic solid support (Florisil). The influence of impregnation was studied in order to improve the adsorption capacity of the material obtained. Impregnation was realized with the help of a rotavapor. Stirring time and temperature used were varied. Ionic liquid-impregnated materials obtained at different conditions of impregnation were characterized using scanning electron microscopy, energy-dispersive X-ray analysis, and Fourier transform infrared spectroscopy. In order to determine the most efficient adsorbent material, the materials obtained were used in the removal process of thallium ions from aqueous solutions, varying the initial concentration of thallium ions and the stirring time used in the adsorption process. It was observed that for the improving the adsorption capacity of the obtained ionic liquid-impregnated material, it is not necessary to increase the stirring time of the impregnation process but to increase the temperature. The experimental data obtained in the adsorption process were fitted with the Langmuir isotherm. Adsorption of thallium ions onto Florisil impregnated with 1-n-hexyl-3-methylimidazolium chloride ionic liquid corresponds to a pseudo-second-order kinetic model.  相似文献   

15.
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   

16.
为了研究不同类型的生物炭对模拟地下水中去除Cr（Ⅵ）的影响，选用杨木、柳木、桃木和松木为原料，分别在300℃和600℃热解温度下，制备不同粒径、经氯化铁改性的和未改性的20种生物炭，设计了一系列批实验，探究不同种类的生物炭对模拟地下水中Cr（Ⅵ）的去除效果；并采用傅里叶变换红外光谱（FTIR）和X射线近边吸收光谱（XANES）研究了生物炭去除Cr（Ⅵ）的机理。结果表明：在300℃下热解制成的改性生物炭，对Cr（Ⅵ）去除率均达到了99.0%以上；和粒径2 mm的生物炭相比，粒径<0.5 mm的生物炭对Cr（Ⅵ）有更好的去除效果；拟一级动力学方程较好地描述了300℃热解温度下杨木铁改性生物炭（FeCl3BC300Y）对Cr（Ⅵ）的去除过程。XANES分析结果表明，FeCl3BC300Y中的铬以三价的形态（Cr（Ⅲ））存在，FTIR分析表明羟基和羧基参与了Cr（Ⅵ）的去除。生物炭通过氧化还原和络合作用去除Cr（Ⅵ）。铁改性生物炭有望作为可渗透反应墙的填充材料，成为修复Cr（Ⅵ）污染地下水的新型材料。  相似文献   

17.
The adsorption of copper(II) onto goethite was studied as a function of pH, total dissolved copper concentration, surface area of goethite, and ionic strength. The adsorption of copper was similar to that of other hydrolyzable metals. A tenfold increase in goethite surface area had a significant effect on the adsorption edge, but a tenfold increase in the ionic strength of the medium did not effect the adsorption edge. The distribution coefficients increase sharply with increase in pH and ranged from 10 to 60,000 ml/g over a range of two and half pH units, depending on the goethite surface area and copper concentration. A tenfold decrease in ionic strength as well as a tenfold increase in surface area of goethite did not have any effect on the magnitude of distribution coefficients. Distribution coefficients were used to calculate the number of protons released per mole of copper adsorbed during the adsorption process. The average number of protons released per mole of copper adsorbed was estimated to be 1.40 ± 0.10.Managed by Martin Marietta Energy System, Inc., for the U.S. Department of Energy under contract no. DE-AC05-840R21400.  相似文献   

18.
This paper presents the first attempt to investigate the potential of Tunisian palygorskite-rich clay (Pal-clay) on the effectiveness of a textile dye “Direct orange 34” (DO34) removal. Important parameters which affect adsorption, such as initial solution pH, contact time, adsorbent mass, initial dye concentration, and temperature, were investigated. The raw Pal-clay was characterized using X-ray diffractometer (XRD), X-ray fluorescence (XRF), Fourier transform infrared spectroscopy (FTIR), cation exchange capacity (CEC), specific surface area (SSA) analysis, and point of zero charge (PZC) determination. The results showed that the Pal-clay has a high selectivity for DO34 and had maximum removal efficiency reaching up to about 91 %. The highest adsorption capacity was obtained at 25 °C and pH of 2. The dye uptake process fitted well to the pseudo-second-order kinetic expression and was best described by the Langmuir and Freundlich isotherms. Intra-particle diffusion studies showed that the adsorption mechanism was not exclusively controlled by the diffusion step and was more likely to be governed by external mass transfer. Thermodynamic parameters such as change in free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) were also calculated. The parameters revealed that the adsorption of dye by the raw clay is spontaneous and exothermic. The results indicate that the Pal-clay has a moderate adsorption capacity towards anionic dye.  相似文献   

19.
Thermally carbonization biochar produced from a traditional Chinese herbal medicine waste (Astragalus mongholicus residue) was investigated for its performance in ciprofloxacin adsorption. Batch sorption experiments were conducted, and scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and Brunauer–Emmett–Teller surface area analyses were employed to characterize the biochar. The results demonstrated that thermal activation process improves the adsorbent characteristics. Biochar produced at 800 °C had the best adsorption capacity, a better pore structure and the largest surface areas. The adsorption process fit well to a pseudo-second-order kinetics model. The adsorption isothermal model results revealed that the adsorption process of ciprofloxacin is described better by the Freundlich isotherm and the type of adsorption is a chemical process. The maximum adsorption of ciprofloxacin occurred at pH 7. The present research demonstrated that A. mongholicus biochar might be an attractive and cost-effective adsorbent with good adsorption performance for removing ciprofloxacin from water solution.  相似文献   

20.
The adsorption behavior of chromate on two variable charge soils (Oxisol and Ultisol) was investigated through batch experiments at different ionic strengths and pH values. The adsorption of chromate on the variable charge soils was found to be strongly dependent on the pH of the soil solutions. A characteristic pH was observed, which corresponds to the intersection of the chromate adsorption—pH curves at different ionic strengths. The characteristic pH values are 5.50 for Oxisol and 5.04 for Ultisol, close to the point of zero salt effect (PZSE) of these soils. The zeta potentials measured for these soils provide the evidences to support the interpretation of the effect of ionic strength on the adsorption of chromate on these variable charge soils. The adsorption behavior of chromate was interpreted by a schematic representation of chromate distribution at increasing ionic strength. The chromate desorption–pH curves were also found to intersect at pH of 5.15 and 4.89 for the Oxisol and Ultisol, respectively. It is considered that chromate adsorption by the variable charge soils was mainly determined by the electrostatic potential on the adsorption plane, which was controlled by the ionic strength of the soil solutions.  相似文献   

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