Polyamine Functionalized Magnetite Nanoparticles as Novel Adsorbents for Cu(II) Removal from Aqueous Solutions

Three novel magnetic adsorbents were synthesized through the immobilization of di-, tri-, and tetraamine onto the surface of silica coated magnetite nanoparticles. The adsorbents were characterized by XRD patterns, FTIR spectroscopy, elemental and thermogravimetric analysis, magnetic measurements, SEM/TEM, EDX spectroscopy, and N₂ adsorption/desorption isotherms. Their capacity to remove copper ions from aqueous solutions was investigated and discussed comparatively. The equilibrium data were analyzed using Langmuir and Freundlich isotherms. The kinetics was evaluated using the pseudo-first-order, pseudo-second-order, and intra-particle diffusion models. The best interpretation for the equilibrium data was given by the Langmuir isotherm for the tri- and tetraamine functionalized adsorbents, while for the diamine functionalized adsorbent the Freundlich model seemed to be better. The kinetic data were well fitted to the pseudo-second-order model. The overall rate of adsorption was significantly influenced by external mass transfer and intraparticle diffusion. It was observed that the adsorption capacity at room temperature decreased as the length of polyamine chain immobilized on the adsorbent surface increased, the maximum adsorption capacities being 52.3 mg g^?1 for 1,3-diaminopropan functionalized adsorbent, 44.2 mg g^?1 for diethylenetriamine functionalized adsorbent, and 39.2 mg g^?1 for triethylenetetramine functionalized adsorbent. The sorption process proved to be highly dependent of pH. The results of the present work recommend these materials as potential candidates for copper removal from aqueous solutions.     

Removal of Lead (II) Ions from Aqueous Solution Using Eggplant Peels Activated Charcoal

The eggplant peel activated charcoal (EPPAC) was investigated as an adsorbent for the removal of lead II ions from aqueous solution. Three methods were tested for the production of eggplant peel activated charcoal (EPPAC) from eggplant peel charcoal (EPPC), yielding three different products; EPPAC-1, EPPAC-2, and EPPAC-3. The difference among the three methods lies in the primary physical mixing of the EPPC with the activating agent (potassium hydroxide) before heating the mixture in a furnace for activation. The removal efficiency of lead II ions by the three adsorbents was 57.7%, 70.0%, and 60.0% for EPPAC-1, EPPAC-2, and EPPPAC-3, respectively. The optimized activation parameters for EPPAC-2 were: activation time 2 hours, activation temperature 700°C, and activation ratio 1:2 (EPPAC: KOH). Scanning electron microscopy (SEM) revealed that EPPAC-2 has the most porous structure. The surface area of EPPAC-2 was measured to be 739 m²/g. Adsorption kinetics of lead (II) is best described by the pseudo-second-order kinetic model with second order rate constant of 1.70 × 10^?3 g/mg.h at room temperature. The adsorption of lead on EPPAC-2 is found to follow the Langmuir isotherm with a maximum adsorption capacity of 1.4 × 10² mg/g.     

Valine-Coated Magnetic Nanoparticles: Synthesis,Characterization, and Application in Removal of Cd(II) Ions from Aqueous Solution

A novel Valine coated magnetic nano-particles (MNPs-Val) has been synthesized for the removal of Cd(II) ions from aqueous solution. The MNPs-Val were developed by electrostatic attraction of valine (C₅H₁₁NO₂) on the bare surface of Fe₃O₄ nanoparticles and characterized by using FT-IR, XRD, SEM, and TEM analysis. The morphology and average particles size 15-27 nm of MNPs-Val were analyzed by SEM and TEM. The coated MNPs were applied for adsorptive removal of Cd(II) ions from aqueous solutions. Factors affecting the adsorption of Cd(II) ions on the MNPs-Val surface such as the pH, temperature, adsorbent dosage, and contact time were investigated which have significant effect on the metal ion removal. The Cd(II) ions adsorption equilibrium on the MNPs-Val could be achieved in 35 min at the optimized pH 5 and follow the pseudo-second order kinetics model. The experimental data for the adsorption of Cd(II) was followed by the Langmuir isotherm and the maximum adsorption capacity was obtained at 0.2 g L^?1 adsorbent dose at 308 K.     

胺化Fe3O4@SiO2纳米颗粒的制备及其对水溶液中Cr(VI)的去除

六价铬(Cr(VI))因其高毒性受到人们广泛关注,为提高吸附法去除Cr(VI)的效率,合成了一种新型核壳结构的聚乙烯亚胺(PEI)功能化复合纳米颗粒(Fe3O4@SiO2–NH2),用于去除水中Cr(VI).研究了磁性纳米颗粒的化学结构、形貌和磁性特性.考察了初始浓度、吸附时间、溶液pH值和无机阴离子对Cr(VI)吸附...     

Removal of Fluoride from Aqueous Solution by CaO Nanoparticles

Abstract

Colloidal particles of CaO were synthesized by the sol-gel method. The particle morphology was characterized by FT-IR, TGA, DTA, and TEM analysis. The ability of the CaO nanoparticles for removal of fluoride from aqueous solution through adsorption has been investigated. All the experiments were carried out by batch mode. The effect of various parameters viz. contact time, pH effect (pH 2–10), adsorbent dose (0.01–0.1 g/100 ml), initial fluoride concentration (10–100 mg/l) and competitive ions has been investigated to determine the adsorption capacity of CaO nanoparticles. Almost complete removal (98%) of fluoride was obtained within 30 minutes at an optimum adsorbent dose of 0.6 g/L for initial fluoride concentration of 100 mg/L. The adsorption isotherm was also studied to find the nature of adsorbate-adsorbent interaction.     

Removal of As(III) from Aqueous Solution Using Functionalized Ultrafine Iron Oxide Nanoparticles

Arsenic toxicity has become a major concern worldwide. Remediation of this problem needs the development of technology with improved materials and systems with high efficiency. We have demonstrated a simple and efficient method for the absolute removal of As(III) from high concentration As(III) treated water with a low contact time period. The process of As(III) adsorption follows pseudo-second-order kinetic model. The mechanism for high-adsorption efficiency is attributed to fatty acid binding domain-mediated surface conjugation of ultrafine Fe₂O₃ nanoparticles with As(III). We have also ensured the simultaneous separation of arsenic sorbed nanoparticles by entrapping them in hydrophilic calcium alginate beads and thereby a pure arsenic free solution has been obtained.     

Removal of Mercury (II) from Aqueous Solution using Chitosan-graft-Polyacrylamide Semi-IPN Hydrogels

Chitosan-graft-polyacrylamide semi-interpenetrating polymer network (IPN) superabsorbent hydrogel was prepared via UV irradiation and N, N′-methylene-bis-acrylamide was used as crosslinker. The product was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), and scanning electron microscopy (SEM). The hydrogels were observed to exhibit as much as 2580.2% swelling under optimum reaction conditions. The hydrogel is an efficient selective sorbent for the removal of mercuric ions (Hg(II)) from aqueous solutions. The mercury sorption capacity under non-buffered conditions is achieved around 9.98 mmol · g^?1 (or 2001.8 mg (mercury)/g (hydrogel)) via the colorimetric method. The kinetic data were fitted to the pseudo second order model. Furthermore, the influence of pH, hydrogel dose, and initial mercury concentration on adsorption capacity of the semi-IPN hydrogel was evaluated. Also, the isothermal adsorption equilibrium data was described using the Langmuir model. Finally, the mercury loaded hydrogel was regenerated without losing its original activity and stability.     

Removal of Copper from Aqueous Amminecopper(II) Solution by Foam Flotation

Abstract

Copper is removed from aqueous amminecopper(II) solution by adsorbing colloid flotation. Iron(III) hydroxide is used as the adsorbing carrier floc, and an anionic surfactant sodium dodecyl sulfate is used as the collector. Optimal flotations are achieved at the pH of maximum adsorption of copper on the resultant flocs. Adsorption of copper on the flocs enhances their floatability. Rapid and efficient removal of copper can be obtained by a batch operation under controlled dosing of iron(III) for samples in various concentrations of total ammonia. A two-step batch method has the advantages of higher efficiency and lower copper residue when dealing with samples of high copper concentration (>200 ppm) and low total ammonia (<0.15 M).     

厌氧颗粒污泥对水中铅离子的吸附与解吸附

采用厌氧颗粒污泥对废水中的Pb2+进行了吸附和解吸附研究. 结果表明,影响Pb2+吸附的主要因素是溶液pH、污泥投加量、Pb2+的初始浓度及接触时间. 处理25 mL Pb2+浓度为100 mg/L的(pH 4~5)模拟废水时,投加0.1 g污泥,污泥吸附容量为121.1 mg/g,对废水中Pb2+的吸附率可达99.5%. 未经烘干处理的颗粒污泥有更强的吸附能力,其吸附过程符合Lagergren二级动力学方程,吸附等温线可由Langmuir和Freundlich方程很好地拟合,相关性良好. 吸附Pb2+后的厌氧颗粒污泥用0.1 mol/L硝酸经3次解吸后,解吸率可达93.11%.     

Lead(II) Adsorption from Aqueous Solution by Poly(ethylene terephthalate)-g-Acrylamide Fibers

In this study, a reactive fibrous adsorbent was prepared by graft copolymerization of Acrylamide (AAm) onto poly(ethylene terephthalate) (PET) fibers and the adsorption properties of Pb(II) ion from aqueous solution by the reactive fibers were examined by batch equilibration technique. The effects of graft yield, pH, adsorption time, initial ion concentration and adsorption temperature on the adsorption amount of Pb(II) ion was studied. The results show that the adsorption amounts of Pb(II) ion increased with grafting yield, shaking time, initial ion concentration and adsorption temperature. Adsorption of Pb(II) ion was strongly affected by pH. A Lagergren pseudo-second-order was the model that best described the adsorption mechanism. It was found that the adsorption isotherm of the Pb(II) ion fit Langmuir-type isotherms. From the Langmuir equation the adsorption capacity was found as 39.57 mg/g fiber for Pb(II) ion for the copolymer with a graft yield of 15.7%. Quantitative desorption of Pb(II) from reactive fibers were found to be 96% by 5 M HNO₃. Five adsorption–desorption cycles demonstrated that the reactive fibers were suitable for repeated use without considerable change in adsorption capacity. The results of the thermodynamic study indicated that the adsorption processes was endothermic and spontaneous.     

Removal of Indigo Carmine and Pb(II) Ion from Aqueous Solution by Polyaniline

In this work, we report the synthesis of polyaniline emaraldine salt (PAni-ES) by a chemical oxidative polymerization method. The obtained PAni-ES samples prepared under different conditions were used for the removal of indigo carmine anionic dye and Pb(II) ion from aqueous solutions. The results also showed that the pseudo–second-order kinetic model fitted better than the data obtained from pseudo–first-order model for the adsorption of anionic dye and Pb(II) ion onto PAni-ES. The fit of the data for indigo carmine and Pb(II) ion adsorption onto PAni-ES suggested that the Langmuir model gave closer fittings than Freundlich model.     

Removal of Pb(II) from Aqueous Solution by Cross-linked Starch Phosphate Carbamate

The adsorption process of Pb(II) ions from aqueous solution by water-insoluble starch phosphate carbamates was investigated. The influences of adsorption conditions, such as adsorption time, adsorbent dose, pH, content of the substituent groups, initial Pb(II) concentration, and temperature, were thoroughly studied. It was shown that an adsorption time of 20 min is sufficient to reach the adsorption equilibrium, the adsorption equilibrium data follow well the Langmuir isotherm model, and the adsorption of Pb(II) ions on cross-linked starch phosphate carbamate is endothermic in nature. For the cross-linked starch phosphate carbamate (CSPC3) with a phosphate group content of 3.10 mmol/g and a carbamate group content of 1.40 mmol/g, the maximum adsorption capacity evaluated from the Langmuir isotherm towards Pb(II) is 2.01 mmol/g. In addition, repeated adsorption/desorption cycles were performed to examine the reusability of adsorbents and the recovery efficiency of Pb(II) ions. The adsorption capacity of Pb(II) ions by CSPC3 decreased from 1.85 to 1.47 mmol/g for three cycles.     

Efficient Removal of Hg(II) by Polymer-Supported Hydrated Metal Oxides from Aqueous Solution

Chelating PS-EDTA resins modified by metal (Fe, Al, and Zr) oxides were used as adsorbents to remove Hg(II) from aqueous solutions. The modified resins were characterized by BET, FTIR, and XPS. The amino, carboxylate, and the metal oxides on resins exhibited a synergistic effect for Hg(II) removal. It was observed that the modification of PS-EDTA resin not only increased the adsorption of Hg(II) but also accelerated the adsorption rate of Hg(II). The equilibrium data of Hg(II) were best described by the Freundlich isotherm, and the kinetics were found to follow the pseudo-second-order kinetic model. Also, thermodynamic parameters showed that Hg(II) adsorption was endothermic and spontaneous in nature. The increasing the concentration (0.1–2.0 g/L) of NaNO₃ in Hg(II) solution did not affect the adsorption of Hg(II). Moreover, the competitive adsorption indicated that the modified resins had higher selectivity towards Hg(II) over Cd(II), Pb(II), Zn(II), or Cu(II) in a binary system. All of the above results indicated that the modified resin was an efficient and reusable adsorbent for Hg(II) removal due to its simple preparation, high adsorption capacity, fast adsorption rate, ionic strength independence, high selectivity, and good reusability. These properties are of potential application in the fixed-bed continuous-flow column for Hg(II) removal from wastewaters.     

Biosorptive Removal of Ni(II) from Aqueous Solution by Caesalpinia bonducella Seed Powder

The present work deals with the use of Caesalpinia bonducella seed powder (CBSP) as a biosorbent for Ni(II) removal from aqueous solution. The nature and morphology of the sorbent were determined using FTIR spectral, SEM, and EDX analysis. The biosorption characteristics of Ni(II) onto CBSP was investigated as a function of pH, biosorbent dosage, contact time, initial metal ion concentration, and temperature. Langmuir and Freundlich isotherms were used to fit the experimental data. The best interpretation for the equilibrium data was given by the Langmuir isotherm. The maximum biosorption capacity was found to be 188.7 mg/g for Ni(II) at pH 5.0 and at 323 K. The equilibrium biosorption data were well fitted with the pseudo-second-order kinetic equation. The values of thermodynamic parameters (ΔG^o, ΔH^o, and ΔS^o) indicated that the biosorption of Ni(II) onto CBSP was feasible, spontaneous and exothermic in nature. The FTIR results revealed that hydroxyl, amine, carboxyl, and carbonyl functional groups are responsible for Ni(II) biosorption onto CBSP.     

Amidoximated Sunflower Stalks (ASFS) as a New Adsorbent for Removal of Cu (II) from Aqueous Solution

A sunflower stalk graft copolymer was prepared by the reaction of ground sunflower stalks (SFS) with acrylonitrile (AN) in aqueous solution initiated by KMnO₄-citric acid (CA) system. It has been shown that the grafting parameters, such as concentration of KMnO₄, AN, and CA, have a significant effect on graft copolymerization. The temperature as well as the duration time of the reaction were studied and also showed a significant effect on the graft copolymerization reaction. The possible reaction was deduced by estimation of nitrogen content. Amidoximation of the grafted stalks was performed by the reaction of grafted SFS with hydroxylamine hydrochloride in alkaline medium to obtain amidoximated sunflower stalks (ASFS). The obtained amidoximated product was detected by FT-IR spectra. The effects of pH and concentration of the adsorbent, ASFS, on adsorption of Cu (II) were studied. The study shows that the ASFS was effectively used in adsorption of Cu (II) ions from aqueous solution. The adsorption data obeyed Langmuir and Freundlich isotherms.     

Fe2+-modified Vermiculite for the Removal of Chromium (VI) from Aqueous Solution

A novel adsorbent: Fe²⁺-modified vermiculite was prepared in a two-step reaction. Adsorption experiments were carried out as a function of pH, contact time, and concentration of Cr(VI). It was found that Fe²⁺-modified vermiculite was particularly effective for the removal of Cr(VI) at pH 1.0. The adsorption of Cr(VI) reached equilibrium within 60 min, and the pseudo-second-order kinetic model best described the adsorption kinetics. The adsorption data follow the Langmuir model more than the Freundlich model. At pH 1.0, the maximum Cr(VI) sorption capacity (Q _max ) was 87.72 mg · g^?1. Desorption of Cr(VI) from Fe²⁺-modified vermiculite using NaOH treatment exhibited a higher desorption efficiency by more than 80%. The sorption mechanisms including electrostatic interaction and reduction were involved in the Cr (VI) removal. The results showed that Fe²⁺-modified vermiculite can be used as a new adsorbent for Cr(VI) removal which has a higher adsorption capacity and a faster adsorption rate.     

Removal of Pb(II) from Aqueous Solutions by using Chitosan Coated Zero Valent Iron Nanoparticles

This study reports the synthesis, characterization, and application of chitosan coated zero valent iron nanoparticles (CTS-Fe⁰) in the removal of Pb(II) from aqueous medium. This nano adsorbent showed a high adsorption capacity and efficient adsorption towards Pb(II) in aqueous medium. Adsorption of Pb(II) on CTS-Fe⁰ obeyed pseudo-second order kinetics and was controlled by a film diffusion process. Among the various isotherm models the experimental data followed the Langmuir isotherm and the maximum adsorption capacity was found to be 666.6 mg/g at pH 5.0 and 318 K. The sorption mean free energy from D-R isotherm was found to be 72, 131, and 177 J/mol at 298, 308, and 318 K, respectively, indicating a physical sorption. The percentage of Pb(II) removal by CTS-Fe⁰ particles is more than 90% at 318 K. The calculated thermodynamic parameters showed that the adsorption of Pb(II) is feasible, spontaneous, and endothermic in nature. Experimental results indicated that the CTS-Fe⁰ appears to be a promising adsorbent for the removal of Pb(II) from aqueous media.     

水溶液中硒化物纳米颗粒的制备与表征

以醋酸铅和氯化镉作为铅源和镉源,自制的Na2SeSO3溶液为硒源,可溶性淀粉为表面活性剂,常温常压下,在水溶液中合成了PbSe和CdSe纳米颗粒.讨论了淀粉溶液浓度、pH值和反应时间等制备工艺参数对硒化物纳米颗粒的生成和颗粒尺寸的影响.用X射线粉末衍射、紫外-可见吸收光谱、Raman光谱与透射电子显微镜等测试手段对所得...     

Continuous Removal of Lead from Aqueous Solutions by Ca(II) Imprinted Chitosan Microspheres Packed Column

The continuous removal of lead from aqueous solutions by Ca(II) imprinted chitosan (Ca(II)-CS) microspheres packed column is carefully investigated in this work. The modified dose-response model and the Thomas model are exploited to evaluate dynamic behaviors of breakthrough curves. The results show 0.257 min of space time is enough for a Ca(II) imprinted chitosan microspheres packed column to realize deep purification of water containing Pb(II). The Thomas rate constants are higher than 3 mL min-1 mg-1. The Modified dose-response model is feasible to predict the breakthrough curve. The reusability is confirmed during a multi-cycle adsorption-desorption process.     

Removal of Basic Dye Crystal Violet from Aqueous Solution by Cu(II)-Loaded Montmorillonite

The effects of contact time, reaction temperature, and ionic strength on crystal violet adsorption onto Cu(II)-loaded montmorillonite were studied. The kinetic experimental data were analyzed using pseudo-first-order, pseudo-second-order, and Elovich equations to examine the adsorption mechanism. The result suggested that the adsorption was best represented by the pseudo-second-order equation. The suitability of the Langmuir, Freundich, and Temkin isotherms to equilibrium data was also investigated at 25°C. The maximum adsorption capacity was 114.3 mg dye/g Cu(II)-loaded montmorillonite at adsorbent concentration 1 g/L. The differential heat of adsorption was evaluated and the result showed that adsorption of crystal violet onto the Cu-loaded sample was chemical in nature. The ionic strength and reaction temperature exhibited an insignificant impact on the crystal violet adsorption. The Cu(II)-loaded montmorillonite could serve as low-cost adsorbents for removing crystal violet from aqueous solution compared to the data reported in the literature.