Fluoride Removal from Aqueous Solutions by Boehmite

Boehmite was used for the removal of fluoride ions from aqueous solutions in a batch system. The pH, contact time, and fluoride concentration in the removal of fluoride ions by boehmite were evaluated. The removal of fluoride ions by boehmite was the highest between the pH values of 4.5 and 7.5. The kinetic fluoride sorption from aqueous solutions by boehmite was best described by the pseudo-second-order model, and equilibrium was reached in about 24 h. The Freundlich model described the isotherm sorption process; the results indicate that the sorption mechanism is chemisorption on a heterogeneous material.     

Removal of Zn from Aqueous Solutions by Low-Rank Coal

The ability of an immature coal (leonardite) to remove zincfrom aqueous solutions was studied as a function of pH,contact time and concentration of metal solutions.Effective removal of Zn²⁺ was demonstrated at pHvalues of 5–6. Kinetic study showed that the adsorption ofZn²⁺ occurs in two phases: a rapid phase followed by aquasi-equilibrium state attained within the first twohours. The adsorption isotherm was measured at 25 °C, using adsorptive solutions at the optimum pH value todetermine the adsorption capacity.     

Removal of Tartrazine from Aqueous Solution by Adsorption on Activated Red Mud

In this study, activated red mud was used to develop an effective adsorbent in order to remove a toxic azo dye (tartrazine E102) from aqueous solutions. To increase the adsorption capacity, the red mud was activated by acid-heat treatment using 20 wt.% HCl (RM-HCl). To establish the optimum operating parameters, the influence of pH, adsorbent dose, contact time, initial dye concentration, and stirring rate was investigated. The adsorption equilibrium was studied using Langmuir, Freundlich, Dubinin-Radushkevich, Temkin isotherm models, and the characteristic parameters for each adsorption isotherm were determined. The kinetics of the adsorption process was analyzed by means of pseudo-first-order and pseudo-second-order models. The maximum removal efficiency obtained under optimum conditions was 84.72%. These results were in accordance with the isotherm and kinetic data. The results suggested that tartrazine adsorption process follows the pseudo-second-order kinetic model and also that fits Langmuir isotherm model. The maximum monolayer adsorption capacity was 136.98 mg/g.     

铁铝柱撑膨润土组成特征及其磷吸附性能研究

利用天然膨润土合成了铁柱撑膨润土（Fe1-Mt、Fe10-M）t、羟基铁膨润土（FeOx-M）t、羟基铝膨润土（AlOx-M）t和羟基铝铁膨润土复合体（AlFe-M）t,对其化学组成和矿物组成等特征进行分析,比较了5种不同铁铝柱撑膨润土对磷污染水体的吸附净化性能,并通过等温吸附试验探讨了柱撑膨润土对磷的吸附机制。结果发现,不同铁铝柱撑均可以增加天然膨润土的层间距,其中以羟基铝铁膨润土复合体的层间距增加最明显,与原土相比增加约为2倍。5种不同铁铝柱撑均能显著增强膨润土对磷污染水体的吸附净化能力,其中以FeOx-Mt的理论磷吸附容量最大,为12.03mg.g-1,其次为Fe10-Mt、AlFe-Mt和AlOx-Mt,吸附等温曲线同时符合Freundlich方程和Langmuir方程,均达显著水平。结果表明,除膨润土层间距外,不同铁铝柱撑膨润土的磷吸附能力主要与铁铝氧化物的含量及铁的存在形态相关。     

Removal of Phosphate from Aqueous Solution by Functionalized Mesoporous Materials

In the present study, the applications of mesoporous materials based on silica, namely post-synthesized, one-pot synthesized, and pure MCM-41, were investigated for the removal of phosphate from aqueous solution. The mesostructures were confirmed by X-ray diffraction, Brunauer?CEmmett?CTeller, Fourier transform spectroscopy, and transmission electron microscopy. The absorptions of phosphate by the mesoporous adsorbents were examined, with different adsorption models used to describe the equilibrium and kinetic data. The maximum adsorption capacities of the mesostructure adsorbents were found to be 45.162, 40.806, and 31.123 mg g^?C1 for the post-synthesized, one-pot synthesized, and pure MCM-41, respectively. The kinetic data showed that the adsorptions of phosphate onto the post-synthesized and pure MCM-41 followed the pseudo-first-order kinetic model, whereas the one-pot synthesized adsorbent was described by the pseudo-second-order model.     

Zinc Removal from the Aqueous Solutions by the Chemically Modified Biosorbents

Biosorbents are the natural origin adsorbents, which popularity in environmental engineering is steadily increasing due to their low price, ease of acquisition, and lack of the toxic properties. Presented research aimed to analyze the possibility of chemical modification of the straw, which is a characteristic waste in the Polish agriculture, to improve its biosorption properties with respect to removal of selected metals from aquatic solutions. Biosorbents used during the tests was a barley straw that was shredded to a size in the range of 0.2–1.0 mm. The biosorption process was performed for aqueous solutions of zinc at a pH 5. Two different modifications of straw were analyzed: esterification with methanol and modification using the citric acid at elevated temperature. The results, obtained during the research, show a clear improvement in sorption capacity of the straw modified by the citric acid. In the case of straw modified with methanol, it has been shown that the effectiveness of zinc biosorption process was even a twice lower with respect to the unmodified straw. Moreover, it was concluded that the removal of analyzed metals was based mainly on the ion-exchange adsorption mechanism by releasing a calcium and magnesium ions from the straw surface to the solution.

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Removal of Arsenic from Aqueous Solutions by Sorption onto Sewage Sludge-Based Sorbent

This study aimed at evaluating and comparing the removal of arsenic from solutions by a low-cost waste-based sorbent, produced by pyrolysing sewage sludge under appropriate conditions, and by a commercially activated carbon. Batch sorption experiments were performed under isothermal conditions (20°C), in order to evaluate the effect of pH on the arsenic sorption kinetics and on the equilibrium sorption capacity of the materials under study. Kinetic data revealed that the arsenic sorption was faster onto the activated carbon than onto the pyrolysed sludge. The sorption process was well described by both the pseudo-first and pseudo-second-order kinetics equations for both materials. Changes in the initial solution pH have distinct effects on the removal of arsenic onto pyrolysed sludge and activated carbon. While for pyrolysed sludge, pH affects essentially the equilibrium time, for activated carbon it affects the sorption capacity. Equilibrium results were well described by both Freundlich and Langmuir isotherm models, although fittings corresponding to the Langmuir isotherm were slightly better. The Langmuir maximum sorption capacity determined for the pyrolysed sludge was 71???g?g^?1, while for activated carbon was 229???g?g^?1. Despite the relative lower capacity of the pyrolysed sludge, the considerable lower cost and the valorisation of the sludge may justify further research on its use for water decontamination.     

Waste-Derived Siliceous Materials as a Novel Sorbent for Removal of Ni2+ from Aqueous Solutions

In the present study, the preparation of sorbent from waste-derived siliceous materials has been investigated for the removal of nickel ion (Ni²⁺) from aqueous solutions. Three types of ashes, i.e., rice husk ash (RHA), palm oil fuel ash (PFA), and coal fly ash (CFA), were used in the preparation of sorbent. Batch studies were carried out to examine the effect of various experimental parameters, i.e., RHA/CFA/PFA ratio in the sorbent preparation, contact time, initial concentration of Ni²⁺, agitation rate, and pH. Among all the ratios of the prepared sorbent, it was found that sorbent containing RHA and PFA gave the highest Ni²⁺ removal efficiency. The optimum conditions for Ni²⁺ removal using RHA/PFA sorbent were obtained at contact time of 30?min, Ni²⁺ concentration of 100?mg/L, agitation rate of 130?rpm, and pH?4. During the optimum condition, more than 90% of Ni²⁺ could be removed in all experiment studies. It was also found that the spent RHA/PFA sorbents had a narrow range of particle size distributions as compared to prepared RHA/PFA sorbent. In addition, the surface morphology of the spent RHA/PFA sorbents had more compact structures.     

Adsorption of Acrylonitrile on Some Soils and Minerals from Aqueous Solutions

Equilibrium and kinetic studies have been made on the adsorption of acrylonitrile(CH2=CHCN) on three soils and four minerals from aqueous solutions.It was shown that the organic matter was the major factor affecting the adsorption process in the soils.The conformity of the equilibrium data to linear type(one soil) and Langmuir type(two soils) isotherms indicated that different mechanisms were involved in the adsorption.This behavior appears bo be related to the hydrophobicity of soil organic matter due to their composition and E4/E6 ratio of humic acids.The adsorption kinetics were also different among the soils,indicating the difference in porosity of organic matter among the soils,and the kinetics strongly affected the adsorption capacity of soils for acrylonitrile.Acrylonitrile was slightly adsorbed from aqueous solutions on pyrophyllite with electrically neutral and hydrophobic nature,and practically not on montmorillonite and kaolinite saturated with Ca.However,much higher adsorption occurred on the zeolitized coal ash,probably caused by high organic carbon content(107g/kg).     

Fluoride Removal from Aqueous Solutions by a Carbonaceous Material from Pyrolysis of Sewage Sludge

Contact time, pH, fluoride concentration, and sorbent dose effects on the removal of fluoride ions by a carbonaceous material obtained from pyrolysis of sewage sludge (CM) were evaluated. Equilibrium was reached after 18?h of contact time and the maximum sorption was found at pH_eq?=?7.06?±?0.08, which corresponds to the zero charge point of the CM. The highest efficiency in the sorption system for fluoride removal (2.84?±?0.03?mg?F^?? $ g_{{CM}}^{{ - 1}} $ ) was found with 0.4?g_CM?L^?1 and with 20?g_CM?L^?1, 82.2?±?0.5% of fluoride was removed. The kinetic data of the process could be fitted to the pseudosecond order and the intraparticle mass transfer diffusion models, whereas isotherm to the Langmuir?CFreundlich equation. These results indicate that the mechanism is chemisorption on a heterogeneous material. Fluoride ions were best partially desorbed using a bicarbonate ions solution and the material was partially regenerated by using a solution of HCl (pH?=?1).     

Competitive Removal of Heavy Metals from Aqueous Solutions by Montmorillonitic and Calcareous Clays

A batch sorption method was used to study the removal of few toxic metals onto the Late Cretaceous clays of Aleg formation (Coniacian–Lower Campanian system), Tunisia, in single, binary and multi-component systems. The collected clay samples were used as adsorbents for the removal of Pb(II), Cd(II), Cu(II) and Zn(II) from aqueous solutions. Results show that the natural clay samples were mainly composed of silica, alumina, iron and magnesium oxides. N₂-adsorption measurements indicated mesoporous materials with modest specific surface area of <71 m²/g. Carbonate minerals were the most influencing parameters for heavy metal removal by natural clays in both single and multi-element systems. The affinity sequence was Pb(II)>Cu(II)>Zn(II)>Cd(II) due to the variable physical properties of the studied metals. The maximum adsorption capacity reached 131.58 mg/g in single systems, but decreased to <50.10 mg/g in mixed systems. In single, binary and muti-element systems, the studied clay samples removed substantial amounts of heavy metals, showing better effectiveness than the relevant previous studies. These results suggest that the studied clay samples of the Late Cretaceous clays from Tunisia can be effectively used as natural adsorbents for the removal of toxic heavy metals in aqueous systems.     

Synthesis and Characterisation of Novel-Activated Carbon from Waste Biomass Pine Cone and Its Application in the Removal of Congo Red Dye from Aqueous Solution by Adsorption

The present study deals with the synthesis and subsequent application of Fe₃O₄@n-SiO₂ nanoparticles for the removal of Cr(VI) from aqueous solutions. Rice husk, an agrowaste material, was used as a precursor for the synthesis of nanoparticles of silica. Synthesized nanoparticles were characterized by XRD and SEM to investigate their specific characteristics. Fe₃O₄@n-SiO₂ nanoparticles were used as adsorbent for the removal of Cr(VI) from their aqueous solutions. The effects of various important parameters, such as initial Cr(VI) concentration, adsorbent dose, temperature, and pH, on the removal of Cr(VI) were analyzed and studied. A pH of 2.0 was found to be optimum for the higher removal of Cr(VI) ions. It was observed that removal (%) decreased by increasing initial Cr(VI) concentration from 1.36?×?10^-2 to 2.4?×?10^-2 M. The process of removal was found to be endothermic, and the removal increased with the rise in temperature from 25 to 45 °C. The kinetic data was better fitted in pseudo-second-order model in comparison to pseudo-first-order model. Langmuir and Freundlich adsorption capacities were determined and found to be 3.78 and 1.89 mg/g, respectively, at optimum conditions. The values of ΔG ⁰ were found to be negative at all temperatures, which confirm the feasibility of the process, while a positive value of ΔH ⁰ indicates the endothermic nature of the adsorption process. The present study revealed that Fe₃O₄@n-SiO₂ nanoparticles can be used as an alternate for the costly adsorbents, and the outcome of this study may be helpful in designing treatment plants for treatment of Cr(VI)-rich effluents.     

Removal of Methylene Blue from an Aqueous Medium Using Atemoya Peel as a Low-cost Adsorbent

Water, Air, & Soil Pollution - The objective of the present study was the synthesis and characterization of chitosan-alginate-based cross-linked copolymer (CACC) for the effective removal of...     

Combined Removal of Zinc (II) and Cadmium (II) from Aqueous Solutions by Adsorption onto High-Calcium Turkish Fly Ash

The aim of this work is the investigation of possible use of flyash in the removal of zinc (Zn²⁺) and cadmium (Cd²⁺) contained in aqueous solutions. Batch adsorption experiments wereperformed in order to evaluate the removal efficiency oflignite-based fly ash. The parameters studied include contact time, pH,temperature, initial concentration of the adsorbate and fly ashdosage. The contact time necessary to attain equilibrium was found to be two hours. Maximum adsorption occurred in the pH range of 7.0 to 7.5. The percent adsorption of Zn²⁺ and Cd²⁺ increased with an increase in concentration of Zn²⁺ and Cd²⁺, dosage of fly ash and temperature. Theapplicability of Langmuir isotherm suggests the formation ofmonolayer coverage Zn²⁺ and Cd²⁺ ions at the outer surface of the adsorbent. Thermodynamic parameters suggested the endothermic nature of the adsorption process. The fly ashwas found to be an metal adsorbent as effective as activated carbon.     

Removal of Denim Blue from Aqueous Solutions by Inorganic Adsorbents in a Fixed-Bed Column

The adsorption behavior of denim blue from aqueous solutions in column systems, using both carbonaceous material and Fe-zeolitic tuff (Fe-Z), was determined. The breakthrough data obtained for denim blue adsorption were fitted to the empty-bed contact time, Bohart?CAdams, Thomas, and Yoon?CNelson models. The parameters such as breakthrough and saturation times, bed volumes, kinetic constants, adsorption capacities, and adsorbent usage rates (AUR) were determined. The results show that the breakthrough time increases proportionally with increasing bed height, but it decreases as the kinetic constant increases. The adsorption capacity for denim blue for carbonaceous material was higher than Fe-Z. AUR was lower for carbonaceous material than Fe-Z. The results indicated that the carbonaceous material from pyrolysis of sewage sludge is a good adsorbent for denim blue removal.     

Removal of Mercury Ions from Mixed Aqueous Metal Solutions by Natural and Modified Zeolitic Minerals

Research works on the removal of mercury from water by zeolitic mineralshow that small quantities of this element are sorbed. In this work the mercury sorption from aqueous solutions in the presence and absence of Cu(II), Ni(II) and Zn(II) onto a Mexican zeolitic mineral unmodified and modified with cysteamine hydrochloride or cystamine dihydrochloride was investigated in acidic pH. The zeolitic minerals were characterized by thermogravimetric analysis, scanning electron microscopy, X-ray diffraction and FTIR. The sorption kinetics behavior and the retention isotherms for mercury were determined in the natural and treated zeolitic mineral samples. It was found that the amounts of sulfur on the modified zeolitic minerals were 0.375 (cysteamine hydrochloride) and 0.475 (cystamine dihydrochloride) mmol g^-1, which were not saturated to their total capacities of adsorption for the maximum concentration used (0.310 mM). Under the experimental conditions, the retention of mercury was the highest for the zeolitic minerals treated with the organic compounds, with adsorption capacities ranging from 0.0107 to 0.0509 mmol Hg g^-1.The retention was not affected by the presence of others heavy metals studied in this work as expected.     

Selective Adsorption of Silver Ions from Highly Acidic Aqueous Solutions by Polymers Containing Multiple Sulfur Groups

A polymer (PDMTD) containing multiple sulfur groups is prepared and used for selective adsorption of silver ion from aqueous solution. The batch adsorption experiments are conducted to research the effects of the different parameters on adsorption of silver ion, including pH, adsorption time, and initial Ag(I) concentration. The maximum uptake of Ag(I) is 127.89 mg/g at pH?=?1. The adsorption equilibrium data are fitted with different isotherm and kinetics models. The results show that the adsorption process of Ag(I) follows a pseudo-second-order kinetic model and Langmuir isotherm mode. Chelation interaction between Ag(I) and sulfur and nitrogen atom is the main adsorption mechanism. PDMTD shows the good selectivity from the coexisting ions and can be reused at least five times. The polymers containing multiple sulfur groups have wide application prospect to selectively capture silver ions from highly acidic aqueous solutions.     

The Adsorption of Fluoride Ion from Aqueous Solution by Activated Alumina

The adsorption of fluoride ion in aqueous solution by using alumina was studied in this research. The experimental resultsindicated that the removal efficiency was influenced significantly by solution pH and the optimum operating pH wasfound to be in the range of 5 to 7. For neutral and acidic solutions, the adsorption capacities of fluoride by alumina wasinterfered by the presence of sulfate. The Langmuir and Freundlich isotherms can well describe the equilibrium behaviorsof the adsorption processes. The experimentally determined lowvalues of activation energy indicate nonspecific adsorption isthe predominant mechanism. The surface reaction-limiting batchkinetic model can adequately describe the removal behaviors offluoride ion by alumina adsorption in the batch system.