Kinetic and equilibrium studies of the removal of Pb from aqueous solutions using Na2SO4-EVA/Cloisite 20A composite

The present work describes the suitability of Na₂SO₄ to improve the wetability of a hydrophobic composite, ethylene vinyl acetate/Cloisite^® 20A, to remove Pb²⁺ ions from aqueous solutions through adsorption. The composite was synthesized via melt-blending method. Scanning electron microscopy showed that suspending the composite in de-ionized water improved porosity resulting from the removal of Na₂SO₄. X-ray diffraction showed that the use of Na₂SO₄ improved the amorphous nature of the composites and hence increased wetability. The holes on the composite improved the contact area between Cloisite^® 20A particles and Pb²⁺ ions. Equilibrium adsorption was achieved in 8 h with a 90% Pb²⁺ ion removal from synthetic wastewater. Kinetic and equilibrium models were applied to determine the type of adsorption mechanism involved. The results showed that the sorption of Pb²⁺ was found to be mainly based on physical interactions and ion-exchange mechanisms. It was established that the adsorption follow pseudo second-order rate equation and intraparticle diffusion was the rate determining step. The results showed that sorption mechanism assumed intraparticle diffusion implying that porous structure of the adsorbent influenced diffusion.     

Synthesis and characterization of poly(hydroxyethyl methacrylate-N-methacryloyl-(l)-glutamic acid) copolymer beads for removal of lead ions

N-methacryloyl-(l)-glutamic acid (MAGA) was synthesized using methacryloyl chloride and l-glutamic acid methyl ester as a metal-complexing ligand and/or comonomer. MAGA was characterized by FTIR and NMR. Spherical beads with an average diameter of 150–200 μm were obtained by suspension polymerization of MAGA and 2-hydroxyethyl methacrylate (HEMA) performed in an aqueous dispersion medium. Poly(HEMA-MAGA) beads were characterized by swelling studies, surface area measurements and elemental analysis. Poly(HEMA-MAGA) beads have a specific surface area of 56.7 m²/g. Poly(HEMA-MAGA) beads were used in the removal studies of Pb²⁺ ions. Adsorption equilibrium was achieved in about 60 min. The adsorption of Pb²⁺ ions onto PHEMA beads was negligible (0.38 mg/g). The MAGA incorporation into the polymer structure significantly increased the lead adsorption capacity (348 mg/g). The adsorption of Pb²⁺ ions increased with increasing pH and reached a plateau value at around pH 5.0. Competitive adsorption of heavy metal ions from synthetic wastewater was also studied. The adsorption capacities are 42.5 mg/g for Pb²⁺, 26.8 mg/g for Hg²⁺ and 17.6 mg/g for Cd²⁺ at 0.5 mmol/l metal concentration. Consecutive adsorption and elution operations showed the feasibility of repeated use for poly(HEMA-MAGA) chelating beads.     

Waste calcite sludge as an adsorbent for the removal of cadmium, copper, lead, and zinc from aqueous solutions

Sludge residues, an industrial waste material for the removal of cadmium (Cd²⁺), copper (Cu²⁺), lead (Pb²⁺), and zinc (Zn²⁺) from aqueous solutions were investigated using batch method. Batch mode experiments were carried out as a function of solution pH, adsorbent dosage, initial concentration, and contact time. The results indicated that the adsorbent showed good sorption potential and maximum metal removal was observed at pH ≥?3. Within 120?min of operation, about 63.7, 95.2, 99.9, and 88.2% of Cd²⁺, Cu²⁺, Pb²⁺, and Zn²⁺ ions were removed from the solutions, respectively. Sorption curves were well fitted to the Langmuir and Freundlich models. The adsorption capacities for Cd²⁺, Cu²⁺, Pb²⁺, and Zn²⁺ ions at optimum conditions were 121.2, 1067.8, 566.4, and 534.2?mg?g^?1, respectively. The kinetics of Cd²⁺, Cu²⁺, Pb²⁺, and Zn²⁺ adsorption from aqueous solutions was analyzed by fitting the experimental data to pseudo-first- and pseudo-second-order kinetic models. However, the pseudo-first-order kinetics model provided much better R ² values and the rate constant was found to be 0.001?min^?1 for Cd²⁺, Cu²⁺, Pb²⁺, and Zn²⁺ ions. The results revealed that sludge residues can adsorb considerable amount of Cd²⁺, Cu²⁺, Pb²⁺, and Zn²⁺ ions and it could be an economical method for the removal of these ions from aqueous systems.     

Synthesis of magnetic crosslinked starch-graft-poly(acrylamide)-co-sodium xanthate and its application in removing heavy metal ions

ABSTRACT

This paper describes the synthesis and characterisation of a magnetic crosslinked starch-graft-poly(acrylamide)-co-sodium xanthate (M-CSAX) nanocomposite based on magnetic starch (MCS), acrylamide (AM) and sodium xanthate that underwent heavy metal ions removal in response to an external magnetic field. The material was prepared using magnetic particle Fe₃O₄ nanoflakes (NFs) together with vinylated starch and poly(acrylamide)-co-sodium xanthate via an ultrasound-assisted radical crosslinking/polymerisation reaction. MCS was synthesised by a direct compounding method using Fe₃O₄ NFs as nuclear and vinylated starch as shell. The obtained M-CSAX has a saturation magnetisation value of 19.21 emu·g^?1. Flocculation experiment results showed that the composites have functions of removing both turbidity and heavy metal ions from aqueous solution, and can adsorb 78.3% of Pb²⁺ and 63% of Cu²⁺ from the corresponding salt solutions. The findings of the present work highlight the potential for using M-CSAX as an effective and recyclable adsorbent for wastewater treatment.     

Surface adsorption of poisonous Pb(II) ions from water using chitosan functionalised magnetic nanoparticles

In this study, chitosan functionalised magnetic nano‐particles (CMNP) was synthesised and utilised as an effective adsorbent for the removal of Pb(II) ions from aqueous solution. The experimental studies reveal that adsorbent material has finer adsorption capacity for the removal of heavy metal ions. Parameters affecting the adsorption of Pb(II) ions on CMNP, such as initial Pb(II) ion concentration, contact time, solution pH, adsorbent dosage and temperature were studied. The adsorption equilibrium study showed that present adsorption system followed a Freundlich isotherm model. The experimental kinetic studies on the adsorption of Pb(II) ions exhibited that present adsorption process best obeyed with pseudo‐first order kinetics. The maximum monolayer adsorption capacity of CMNP for the removal of Pb(II) ions was found to be 498.6 mg g⁻¹. The characterisation of present adsorbent material was done by FTIR, energy disperse X‐ray analysis and vibrating sample magnetometer studies. Thermodynamic parameters such as Gibbs free energy (ΔG °), enthalpy (ΔH °) and entropy (ΔS °) have declared that the adsorption process was feasible, exothermic and spontaneous in nature. Sticking probability reported that adsorption of Pb(II) ions on CMNP was favourable at lower temperature and sticking capacity of Pb(II) ions was very high.Inspec keywords: adsorption, lead, wastewater treatment, monolayers, Fourier transform infrared spectra, X‐ray chemical analysis, magnetometers, pHOther keywords: poisonous Pb(II) ions surface adsorption, chitosan functionalised magnetic nanoparticle, CMNP, Pb(II) ions removal, aqueous solution, finer adsorption capacity, heavy metal ion removal, contact time, solution pH, adsorbent dosage, adsorption equilibrium, Freundlich isotherm model, pseudofirst order kinetics, monolayer adsorption capacity, FTIR, energy disperse X‐ray analysis, vibrating sample magnetometer study, thermodynamic parameter, sticking probability, Pb(II) ions sticking capacity, initial Pb(II) ion concentration     

Novel negatively charged hybrids. 3. Removal of Pb2+ from aqueous solution using zwitterionic hybrid polymers as adsorbent

Using zwitterionic hybrid polymers as adsorbent, the adsorption kinetics and isotherm, thermodynamic parameters of ΔG, ΔH and ΔS for the removal of Pb²⁺ from aqueous solution were investigated. It is indicated that the adsorption of Pb²⁺ ions on these zwitterionic hybrid polymers followed the Lagergren second-order kinetic model and Freundlich isotherm model, demonstrating that the adsorption process might be Langmuir monolayer adsorption. The negative values of ΔG and the positive values of ΔH evidence that Pb²⁺ adsorption on these zwitterionic hybrid polymers is spontaneous and endothermic process in nature. Moreover, the zwitterionic hybrid polymers produced reveal relatively higher desorption efficiency in 2 mol dm^?3 aqueous HNO₃ solution, indicating that they can be recycled in industrial processes. These findings suggest that these zwitterionic hybrid polymers are the promising adsorbents for Pb²⁺ removal and can be potentially applied in the separation and recovery of Pb²⁺ ions from the waste chemicals and contaminated water of lead-acid rechargeable battery.     

Facile preparation of magnetic sodium alginate/carboxymethyl cellulose composite hydrogel for removal of heavy metal ions from aqueous solution

A novel magnetic polysaccharide composite hydrogel was successfully constructed by using sodium alginate (SA) and carboxymethyl cellulose (CMC) as the backbone and filled with in situ Fe₃O₄ nanoparticles, which was then employed for removal of heavy metal ion from aqueous solution. The obtained magnetic SA/CMC composite hydrogel was characterized by Fourier transform infrared spectroscopy, fluorescence microscope, thermogravimetric and vibrating sample magnetometer. Effect of contact time, pH and adsorbent dosage on the adsorption of heavy metal ions by the magnetic SA/CMC hydrogel have also been studied. The results show that the prepared magnetic SA/CMC hydrogel can be effectively utilized in the removal of heavy metal ions from aqueous solution. The maximal adsorption capacity of Mn(II), Pb(II), and Cu(II) as calculated from the Langmuir model were 71.83, 89.49, and 105.93 mg/g, respectively. The adsorption process of the magnetic SA/CMC hydrogel on the heavy metal ions can be attributed to ion exchange and chemical adsorption. What’s more, the magnetic hydrogel exhibited high efficiency after four cycles, which indicating it offers great potential for practical application in the removal of heavy metal ions from aqueous solution.

     

铅锌尾矿免烧吸附砖的制备与研究

为了提供一种铅锌尾矿用于制备建材的可行方法,利用铅锌尾矿、硅微粉和水泥制备免烧砖,研究了硅微粉、水泥等胶结物对重金属离子的固化行为,并探究该免烧砖作为重金属离子吸附剂的可能性.采用X射线荧光光谱仪、电感耦合等离子发射光谱仪及扫描电子显微镜研究了免烧砖在不同条件(p H、吸附时间及初始浓度)对废水中Pb2+的吸附行为.结果表明:铅锌尾矿掺量为70%,硅微粉为20%,制备的免烧砖强度符合MU20等级;水化产物与尾矿中的重金属形成沉淀物,有效固化重金属离子;同时,该免烧砖可作为优良的吸附基体,对废水中的铅具有高效的去除能力,在p H为5、吸附时间为90 min、含铅废水初始质量浓度50 mg/L时,免烧砖对Pb2+的吸附效率达到96%.因此,适量的硅微粉及水泥可以提高尾矿免烧砖对Pb2+的吸附,该免烧砖有望用在江河堤坝等场合.     

Optimization,Kinetics, and Equilibrium Studies on the Removal of Lead(II) from an Aqueous Solution Using Banana Pseudostem as an Adsorbent

Natural adsorbents such as banana pseudostem can play a vital role in the removal of heavy metal elements from wastewater. Major water resources and chemical industries have been encountering difficulties in removing heavy metal elements using available conventional methods. This work demonstrates the potential to treat various effluents utilizing natural materials. A characterization of banana pseudostem powder was performed using environmental scanning electron microscopy (ESEM) and Fourier-transform infrared (FTIR) spectroscopy before and after the adsorption of lead(II). Experiments were carried out using a batch process for the removal of lead(II) from an aqueous solution. The effects of the adsorption kinetics were studied by altering various parameters such as initial pH, adsorbent dosage, initial lead ion concentration, and contact time. The results show that the point of zero charge (PZC) for the banana pseudostem powder was achieved at a pH of 5.5. The experimental data were analyzed using isotherm and kinetic models. The adsorption of lead(II) onto banana pseudostem powder was fitted using the Langmuir adsorption isotherm. The adsorption capacity was found to be 34.21 mg·g^–1, and the pseudo second-order kinetic model showed the best fit. The optimum conditions were found using response surface methodology. The maximum removal was found to be 89%.     

Efficient removal of heavy metal ions from aqueous solution using salicylic acid type chelate adsorbent

In this study, 5-aminosalicylic acid was successfully grafted onto the poly(glycidyl methacrylate) (PGMA) macromolecular chains of PGMA/SiO₂ to obtain a novel adsorbent designated as ASA-PGMA/SiO₂. The adsorption properties of ASA-PGMA/SiO₂ for heavy metal ions were studied through batch and column methods. The experimental results showed that ASA-PGMA/SiO₂ possesses strong chelating adsorption ability for heavy metal ions, and its adsorption capacity for Cu²⁺, Cd²⁺, Zn²⁺, and Pb²⁺ reaches 0.42, 0.40, 0.35, and 0.31 mmol g⁻¹, respectively. In addition, pH has a great influence on the adsorption capacity in the studied pH range. The adsorption isotherm data greatly obey the Langmuir and Freundlich model. The desorption of metal ions from ASA-PGMA/SiO₂ is effective using 0.1 mol l⁻¹ of hydrochloric acid solution as eluent. Consecutive adsorption-desorption experiments showed that ASA-PGMA/SiO₂ could be reused almost without any loss in the adsorption capacity.     

功能化SBA-15介孔材料的制备及其吸附性能研究

硅基介孔材料因其特有的特性,被用于去除废水中重金属离子的吸附剂.为了提高对目标污染物的吸附容量, 本文采用一步法和两步法制备了氨基或巯基功能化SBA-15介孔材料,利用傅里叶红外光谱仪、场发射扫描电镜、X射线衍射仪和氮气吸附脱附表征测试了材料的化学组成、微观形貌和物相结构.测试结果显示经功能化处理后的样品成功地接枝氨基或巯基功能基团.研究发现,经功能化处理后,材料的骨架结构及介孔孔道均未被破坏,但有序性下降且出现少许团聚,物性参数也有一定程度下降,功能化材料对Zn²⁺、Pb²⁺、Cr³⁺和Cu²⁺的吸附率均有大幅度提高.经氨基或巯基功能化后,SBA-15介孔材料对水体中重金属离子的吸附率有很大提高,但一步法制备的功能化硅基介孔材料因模板剂去除不彻底而影响了对重金属离子的吸附效率,两步法制备的功能化硅基介孔材料对重金属离子的吸附效果更好,说明本文的功能化硅基介孔材料工艺是可行有效的,但两步法合成的功能化介孔材料具有更好的吸附效果.     

Selective removal of heavy metal ions in aqueous solutions by sulfide-selector intercalated layered double hydroxide adsorbent

Remaining largely under-appreciated, a majority of metal ion sorbents are limited in their target selectivity. In this work, a 3D sulfide intercalated NiFe-layered double hydroxide (NFL-S) hierarchical sorbent has been synthesized for selective heavy metal removal. The intercalation of sulfurated groups in the interlayer of the layered double hydroxide (LDH) nanosheets endows NFL-S as a selective heavy metal ion filter; the selectivity of NFL-S for heavy metals is in the order of Pb²⁺ > Cu²⁺ ≥ Zn²⁺ > Cd²⁺> Mn²⁺, and NFL-S has high k_d values for Pb²⁺ (∼10⁶ mL/g) and Cu²⁺ (∼10⁵ mL/g). Scanning electron microscopy, X-ray photoelectron spectroscopy and powder X-ray diffraction were used to analyze the composition of the as-prepared nanoadsorbent. The selective adsorption behavior was systematically studied using batch experiments, and the performance was evaluated through kinetic and isotherm studies. Moreover, the adsorption mechanism of heavy metals by NFL-S through surface complexation was also investigated, which shows great potential for water decontamination.     

The study of adsorption characteristics Cu and Pb ions onto PHEMA and P(MMA-HEMA) surfaces from aqueous single solution

The adsorption characteristics of Cu²⁺ and Pb²⁺ ions onto poly2-hydroxyethyl methacrylate (PHEMA) and copolymer 2-hydroxyethyl methacrylate with monomer methyl methacrylate P(MMA-HEMA) adsorbent surfaces from aqueous single solution were investigated with respect to the changes in the pH of solution, adsorbent composition (changes in the weight percentage of MMA copolymerized with HEMA monomer), contact time and the temperature in the individual aqueous solutions. The linear correlation coefficients of Langmuir and Freundlich isotherms were obtained. The results revealed that the Langmuir isotherm fitted the experimental results better than the Freundlich isotherm. Using the Langmuir model equation, the monolayer adsorption capacity of PHEMA surface was found to be 0.840 and 3.037 mg/g for Cu²⁺ and Pb²⁺ ions and adsorption capacity of (PMMA-HEMA) was found to be 31.153 and 31.447 mg/g for Cu²⁺ and Pb²⁺ ions, respectively. Changes in the standard Gibbs free energy (ΔG⁰), standard enthalpy (ΔH⁰) and standard entropy (ΔS⁰) show that the adsorption of mentioned ions onto PHEMA and P(MMA-HEMA) are spontaneous and exothermic at 293–323 K.     

Montmorillonite surface properties and sorption characteristics for heavy metal removal from aqueous solutions

Surface properties of montmorillonite (MMT) and its adsorption characteristics for heavy metals have been investigated with nickel and copper as sorbate from aqueous solutions. Employing the potentiometric and mass titration techniques in batch experimental methods, the point of zero charge (PZC) and point of zero net proton charge (PZNPC) of MMT edges at different ionic strengths present pH_PZC and pH_PZNPC to be 3.4 ± 0.2. A crossing point was observed for the proton adsorption vs. pH curves at different ionic strengths of KCl electrolyte and in investigating MMT remediation potentialities as sorbent for heavy metals polluted waters, the effects of heavy metal concentration, pH, MMT dosage, reaction time and temperature for Cu²⁺ and Ni²⁺ uptake were studied. The sorption of metal ions by MMT was pH dependent and the adsorption kinetics revealed sorption rate could be well fitted by the pseudo-second-order rate model. The data according to mass transfer and intraparticle diffusion models confirmed diffusion of solutes inside the clay particles as the rate-controlling step and more important for the adsorption rate than the external mass transfer. Adsorption isotherms showed that the uptake of Cu²⁺ and Ni²⁺ could be described by the Langmuir model and from calculations on thermodynamic parameters, the positive ΔG° values at different temperatures suggest that the sorption of both metal ions were non-spontaneous. Change in enthalpy (ΔH°) for Ni²⁺ and Cu²⁺ were 28.9 and 13.27 kJ/mol K respectively, hence an endothermic diffusion process, as ion uptake increased with increase in temperature. Values of ΔS° indicate low randomness at the solid/solution interface during the uptake of both Cu²⁺ and Ni²⁺ by MMT. Montmorillonite has a considerable potential for the removal of heavy metal cationic species from aqueous solution and wastewater.     

Comparative and competitive adsorption of cadmium, copper, nickel, and lead ions by Iranian natural zeolite

The competitive adsorption behavior of cadmium (Cd²⁺), copper (Cu²⁺), nickel (Ni²⁺), and lead (Pb²⁺) ions using Iranian natural zeolite has been studied in order to determine its applicability in treating industrial wastewater. Tests to determine both the rate of adsorption and the uptake at equilibrium were performed under batch conditions from single- and multi-component solutions. The optimum conditions for the treatment process were investigated by observing the influence of pH levels, the presence of competing ions, varying the mass of zeolite and different contact time. Adsorption kinetics of the zeolite followed first-order kinetics, showing about 100 % of Pb²⁺ removal within 40 min and reaching an equilibrium state within 24 h for Cd²⁺, Cu²⁺, and Ni²⁺. The results indicated that removal of metals from single- and multi-component solutions is best described by a Freundlich isotherm, in which the distribution coefficient was in the following order: Pb²⁺ > Cu²⁺ > Cd²⁺ > Ni²⁺. In the multi-component solutions, metals exhibit competitive adsorption on the zeolite. The adsorption is reduced to 90, 53, 30, and 22 % of single component of Cu²⁺, Ni²⁺, Cd²⁺, and Pb²⁺, respectively. However, the total adsorption was higher than single component. Finally, soil solution saturation indices and speciation of metals was assessed using Visual MINTEQ 2.6 software, and probability of precipitation of minerals supported by scanning electron microscopy. The research indicates that Cd²⁺ and Ni²⁺ retention by zeolite can be viewed as the result of ion exchange reaction, but Pb²⁺ and Cu²⁺ retention is both due to ion exchange and precipitation. These results show that Iranian natural zeolite particularly effective in removing cationic heavy metal species from industrial wastewater.     

Removal of heavy metal lead(II) using nanoscale zero-valent iron with different preservation methods

In this study, different nanoscale zero-valent irons (nZVI) were prepared in order to improve their stability and reactivity to heavy metal lead (Pb (II)). The composition, particle size and morphology of obtained nZVI were characterized by X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscope (SEM). The effects of nZVI dosage, pH, initial Pb (II) concentration and reaction time on the removal efficacy of Pb (II) were investigated. The results show that undried nZVI has more active sites due to its weaker oxidation, and thus the removal efficiency of Pb(II) by undried nZVI was higher than that by dried nZVI. As a result, the same removal efficiency could be achieved with the use of less undried nZVI for the identical concentration of Pb(II). Furthermore, the experimental procedure could be apparently simplified, which eliminates the steps of washing, separation and dehydration compared with the traditional preparation method. The experimental data could be well fitted by the Langmuir adsorption isotherm model, and the maximum adsorption capacity of dried and undried nZVI is 671.14 and 807.23?mg·g^?1 at pH 6, respectively. The experimental data followed the pseudo second-order kinetic model with a kinetic constant of 7.65?×?10^?4 and 1.39?×?10^?3 for undried and dried nZVI, respectively. In conclusion, undried nZVI had high adsorption capacity and adsorption rate for Pb(II) in the solution.     

Nano‐zero valent iron impregnated cashew nut shell: a solution to heavy metal contaminated water/wastewater

The present research is focused on the removal of Zn(II) ions from aqueous solution using nano zero‐valent iron impregnated cashew nut shell (NZVI‐CNS). The present system was investigated in batch mode operation. NZVI‐CNS was prepared by the liquid‐phase reduction process. The results showed that the NZVI‐CNS exhibited superior adsorption capacity for the removal of Zn(II) ions. Adsorption isotherm and kinetic models were applied to explain the nature of the adsorption process. Adsorption kinetic data followed the pseudo‐first order kinetic model. Moreover, the equilibrium adsorption data were best fitted with a Freundlich model. Langmuir monolayer adsorption capacity was calculated as 94.46 mg of Zn(II) ions/g of NZVI‐CNS. The thermodynamic parameters explain that the present adsorption system was measured as feasible and spontaneous. This newly prepared adsorbent can be successfully applied for the different industrial wastewater treatment. Finally, the exploration asks about contemplated that NZVI‐CNS has exhibited unrivalled adsorption limit. Additionally, NZVI‐CNS is believed to be extremely green and monetarily neighbourly help for wastewater treatment. The results indicate that the feasible approach could be applied in agricultural waste biomass materials for the productive expulsion of heavy metals from aqueous solution and reusing agricultural wastes to facilitate their disposal problem.Inspec keywords: wastewater treatment, contamination, zinc, reduction (chemical), adsorption, monolayers, renewable materialsOther keywords: nano zero‐valent iron impregnated cashew nut shell, aqueous solution, Zn(II) ion removal, NZVI‐CNS, batch mode operation, liquid‐phase reduction process, adsorption capacity, adsorption isotherm models, adsorption kinetic models, adsorption kinetic data, adsorption process, pseudo‐first order kinetic model, equilibrium adsorption data, Freundlich model, Langmuir monolayer adsorption capacity, thermodynamic parameters, adsorption system, industrial wastewater treatment, agricultural waste biomass materials, productive expulsion, heavy metals, waste disposal, Zn     

Adsorption study of Pb<Superscript>2+</Superscript> ions on nanosized SnO<Subscript>2</Subscript>, synthesized by self-propagating combustion reaction

Novel combustion synthetic route for the synthesis of nanosized SnO₂ is reported. X-ray, tap and powder densities of SnO₂ are calculated. Adsorption of Pb²⁺ ions on combustion derived nanosized SnO₂ is studied. The as synthesized SnO₂ and lead ions adsorbed SnO₂ are characterized by X-ray diffraction (XRD), scanning electron micrograph (SEM), and infrared spectroscopic (IR) techniques. The eluent is characterized by atomic absorption spectroscopy (AAS) and solution conductivity (SC) to know the reduction in the concentration and increase in conductance of lead solution after adsorption on the SnO₂ surface. The potential use of solid adsorbents for the adsorption of heavy metal pollutants is envisaged in the present work.     

Synthesis of biosurfactant‐coated magnesium oxide nanoparticles for methylene blue removal and selective Pb2+ sensing

Dyes and lead (Pb²⁺) are toxic compounds that can contaminant water. In this study, magnesium oxide (MgO) nanoparticles (NPs) prepared using clove, i.e. Syzygium aromaticum extract [clove extract (CE)] were used for methylene blue (MB) removal and Pb²⁺ ion sensing in aqueous solution. Maximum 90% MB removal was achieved using MgO NPs. The MB adsorption on MgO NPs surface followed second‐order kinetics and Langmuir isotherm. MB dye was adsorbed as a monolayer on the surface of MgO NPs with maximum adsorption capacity, 5555 mg g⁻¹. MgO NPs were also able to selectively detect lead (Pb²⁺) in 1 nM–200 µM range with 24 µM (3σ) limit of detection. So, CE prepared MgO NPs are useful for MB dye adsorption and metal ion sensing applications.Inspec keywords: magnesium compounds, nanoparticles, dyes, lead, chemical sensors, adsorptionOther keywords: biosurfactant‐coated magnesium oxide nanoparticles, methylene blue removal, selective lead sensing, dyes, toxic compounds, Syzygium aromaticum extract, clove extract, MB adsorption, second‐order kinetics, Langmuir isotherm, maximum adsorption capacity, MgO, Pb²⁺      

Poly(hydroxyethyl methacrylate) nanobeads containing imidazole groups for removal of Cu(II) ions

Poly(hydroxyethyl methacrylate) (PHEMA) nanobeads with an average size of 300 nm in diameter and with a polydispersity index of 1.156 were produced by a surfactant free emulsion polymerization. Specific surface area of the PHEMA nanobeads was found to be 996 m²/g. Imidazole containing 3-(2-imidazoline-1-yl)propyl(triethoxysilane) (IMEO) was used as a metal-chelating ligand. IMEO was covalently attached to the nanobeads. PHEMA-IMEO nanobeads were used for the removal of copper(II) ions from aqueous solutions. To evaluate the degree of IMEO loading, the PHEMA nanobeads were subjected to Si analysis by using flame atomizer atomic absorption spectrometer and it was estimated as 973 µmol IMEO/g of polymer. The PHEMA nanobeads were characterized by transmission electron microscopy and fourier transform infrared spectroscopy. Adsorption equilibrium was achieved in about 8 min. The adsorption of Cu²⁺ ions onto the PHEMA nanobeads was negligible (0.2 mg/g). The IMEO attachment into the PHEMA nanobeads significantly increased the Cu²⁺ adsorption capacity (58 mg/g). Adsorption capacity of the PHEMA-IMEO nanobeads increased significantly with increasing concentration. The adsorption of Cu²⁺ ions increased with increasing pH and reached a plateau value at around pH 5.0. Competitive heavy metal adsorption from aqueous solutions containing Cu⁺, Cd²⁺, Pb²⁺ and Hg²⁺ was also investigated. The adsorption capacities are 61.4 mg/g (966.9 µmol/g) for Cu²⁺; 180.5 mg/g (899.8 µmol/g) for Hg²⁺; 34.9 mg/g (310.5 µmol/g) for Cd²⁺ and 14.3 mg/g (69 µmol/g) for Pb²⁺. The affinity order in molar basis is observed as Cu²⁺ > Hg²⁺ > Cd²⁺ > Pb²⁺. These results may be considered as an indication of higher specificity of the PHEMA-IMEO nanobeads for the Cu²⁺ comparing to other ions. Consecutive adsorption and elution operations showed the feasibility of repeated use for PHEMA-IMEO nanobeads.