Sorbent Dosage Research Articles

Humic acid and nano-zeolite NaX as low cost and eco-friendly adsorbents for removal of Pb (II) and Cd (II) from water: characterization, kinetics, isotherms and thermodynamic studies

Humic acid as a green-sorbent was synthesized from marine sediments. While kaolin was modified to nano-zeolite NaX. Different tools such as FT-IR, SEM, EDX and XRD were applied to confirm the characteristics of the generated green-sorbents. Different factors such as pH, contact time, sorbent dosage, initial metal ion concentration, temperature and interfering ions were carefully examined and used to optimize the batch adsorption process for Cd2+ and Pb2+. A small dose of nano-zeolite of 100 mg was required to attain the maximum adsorption of Pb2+ at pH about 7, shacking time at 60 min and Pb2+ concentration at 30 ppm. Also, the maximum sorption capacity of Cd2+ ions on nano-zeolite was achieved in a neutral medium and very short contact time implying the economic feasibility of the adsorption process. In the case of humic acid, the maximum removal capacity for Pb2+ and Cd2+ was operated at acidic medium and shacking time was 40 min. Metal ions remediation results were evaluated by some adsorption isotherm models at different temperatures. The kinetic and thermodynamic variables were also computed. The data fitted very well with the linear Langmuir and the pseudo-second-order model implying a favourable adsorption process. The sorption of Cd2+ and Pb2+ was regulated by both external mass transfer and intraparticle diffusion steps over the whole range of concentrations, as shown by the results. The metal ions removal percentage from four real water samples by green sorbents were applied and provides good evidence of two sorbents as promising eco-sorbent for removal of heavy metal ions.

Synthesis of hybrid biosorbent based on 1,2-cyclohexylenedinitrilotetraacetic acid modified crosslinked chitosan and organo-functionalized calcium alginate for adsorptive removal of Cu(II)

The present study is based on the synthesis of a novel hybrid biosorbent using 1,2-cyclohexylenedinitrilotetraacetic acid modified crosslinked chitosan and amino-thiocarbamate moiety functionalized sodium alginate (CDTA-CS/TSC-CA). The fabricated sorbent was employed to investigate the efficient recovery of Cu(II) from aqueous media. CDTA-CS/TSC-CA was characterized using Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM). Analysis confirmed the successful modification of both biopolymers and subsequent loading of Cu(II) ions. CDTA-CS/TSC-CA was casted in the form of hydrogel beads having different CDTA-CS to TSC-CA mass ratios i.e., 10.0–40.0% by mass. The hydrogel beads 4CDTA-CS/TSC-CA with CDTA-CS/TSC-CA mass ratio of 40.0% was found most effective for copper sorption. Equilibrium sorption results showed that initial concentration of copper, medium pH, contact time, sorbent dosage and temperature influenced the sorption capacity (qe). Rate of sorption data was interpreted using different kinetic models and found best fitted with pseudo second order rate expression (R2 ≈ 0.99), illustrating that the rate determining step includes the electron density transfer from sorbent coordination sites to central copper ions. Crank's RIDE equation and Elovich chemisorption model (ECM) revealed the presence of two sorption phases, initially rapid sorption followed by comparatively a slow uptake. Equilibrium sorption data was well depicted by Langmuir model and maximum monolayer adsorption capacity (qm) was computed as 276.53 mg·g−1 at 298 K. Standard Gibbs free energy change, ∆G° (−19.99, −20.18 and −20.36 kJ/ mol), standard enthalpy change, ∆H° (−8.95 kJmol) and standard entropy change, ∆S° (0.04 kJ/mol K−1) values suggested that the adsorption process is spontaneous and exothermic. Hence, 4CDTA-CS/TSC-CA was found efficient biosorbent for copper removal from its dilute effluents.

Efficient biosorption of hexavalent chromium from water by modified arecanut leaf sheath

In this work, the excision of hexavalent chromium (Cr(VI)) was studied from an aqueous solution using the chemically modified arecanut leaf sheath (CALS) as a novel bio-adsorbent. The as-prepared adsorbent was characterized by using instrumental methods including Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). The effect of several factors, including solution pH, contact time, and sorbent dosages were examined to identify the optimum condition for the sorption ability. The optimal pH of Cr(VI) biosorption was 2.0, and equilibrium was reached in 150 min. Adsorption was shown to be pseudo-second-order in kinetic investigations, and the Langmuir isotherm with maximal adsorption efficiency was determined as 109.89 mg/g. The spent biosorbent can be easily regenerated and reused. For the biosorption of oxyanions of chromium, both electrostatic attraction and ligand exchange mechanism play critical roles. From the results, the CALS appears to be a potential low-cost effective sorbent to remove Cr (VI) from water.

Core-shell magnetic molecularly imprinted polymer for selective recognition and detection of sunset yellow in aqueous environment and real samples

Magnetic Molecularly imprinted polymers (MMIPs) have been recently recognized as an exceptional tool for monitoring and decontamination of environmental and biological samples of diverse nature. Based on the potential applications as sorbents and biomimetic sensors, herein, a core-shell magnetic-molecularly imprinted polymer (MMIP) was developed as a selective material for separation and sensing of sunset yellow (SY) dye in an aqueous environment and real samples. The MMIP was synthesized via precipitation polymerization using SY as a template, MAA as a functional monomer (chosen based on simulation studies), EGDMA as a cross-linking agent, and AIBN as an initiator. To elaborate the specificity of MMIP, a comparative agent, magnetic non-imprinted polymer (MNIP) was also synthesized. The XRD results showed that the MMIP showed both crystalline and amorphous structure attributed to the presence and polymeric and non-polymeric groups. The FTIR spectra confirmed synthesis of intermediate and final MMIP product. The SEM results showed spherical morphology and porous structure of the MMIP with an average particle size of 0.636 μm in diameter. The MMIP was first employed as a sorbent for the removal of SY from the aqueous environment. The binding experiments performed at optimized operating conditions (pH 2; time 30 min; sorbent dosage 3 mg; sorbate concentration 80 ppm) showed more selectivity when compared with MNIP. The data fitted best to Langmuir's sorption isotherm (Qo 359.8 mg/g) and followed the pseudo-second-order kinetic model. The synthesized MMIP was also used as an electrochemical sensor for detection of SY dye in the aqueous environment, which exhibited a linear range of detection as (1.51 × 10−6 – 1.5 × 10−3 M). The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.00413 M and 0.0137 M, respectively. While the R2 value was found to be 0.997 at optimized analytical conditions. These results suggested that the synthesized MMIP can be applied for the selective separation and quantification of SY dye in sample of diverse nature.

Sulfonated calixarene modified Poly(methyl methacrylate) nanoparticles:A promising adsorbent for Removal of Vanadium Ions from aqueous media

The poly (methyl methacrylate) (PMMA)-based nanoparticle was synthesized by surfactant-free emulsion polymerization method and then post modified with Calixarene using (3-Aminopropyl)triethoxysilane organo-silane as a linker after OH-treatment. The prepared structure was applied for efficient adsorption of Vanadium ions in the aqueous solution after characterization by FT-IR, SEM, TEM, DLS, and EDX. Additional investigations discovered that the prepared adsorbent has a good capacity to adsorb vanadium ions. The effect of key experimental factors was studied to find the optimal point of adsorbent efficiency including the initial concentration of analyte, sorbent dosage, pH of the solution, contact time, and type/quantity of the eluents. It was specified, the maximum adsorption capacity for the synthesized nanoparticles was obtained about 322 mg g−1. The adsorption mechanism was revealed that the model of Langmuir isotherm well-matched compared to the others due to the calculated equilibrium data. Besides, the kinetics of the adsorption process was fitted with pseudo-second-order. Eventually, the prepared adsorbent was successfully applied in vanadium adsorption from real water media.

Dried Brown Seaweed's Phytoremediation Potential for Methylene Blue Dye Removal from Aquatic Environments.

The dried form of the brown seaweed Sargassum latifolium was tested for its ability to remove toxic Methylene Blue Dye (MBD) ions from aqueous synthetic solutions and industrial wastewater effluents. In a batch adsorption experiment, different initial concentrations of MBD (5, 10, 20, 30, and 40 mg L−1), sorbent dosages (0.025, 0.05, 0.1, 0.2, 0.3, 0.4, and 0.5 g L−1), contact time (5, 10, 15, 30, 60, 120 min), pH (3, 5, 8, 10, and 12), and temperature (30, 40, 50, 60 °C) were observed. Dried powder of S. latifolium was characterized before and after adsorption of MBD using different techniques, such as FTIR, SEM, UV visible spectral examination, and BET techniques. The BET surface area suggests the formation of S. latifolium was 111.65 m2 g−1, and the average pore size was 2.19 nm. The obtained results showed that at an MBD concentration of 40 mg L−1, the adsorption was rapid in the first 5, 10, and 15 min of contact time, and an equilibrium was reached in about 60 and 120 min for the adsorption. At the optimum temperature of 30 °C and the adsorbent dose of 0.1 g L−1, approximately 94.88% of MBD were removed. To find the best-fit isotherm model, the error function equations are applied to the isotherm model findings. Both Tempkin and Freundlich isotherm models could appropriate the equilibrium data, as well as the pseudo 2nd order kinetics model due to high correlation coefficients (R2). Thermodynamic and Freundlich model parameters were assessed and showed that the mechanism of the sorption process occurs by an endothermic and physical process. According to the results of the experiments, S. latifolium is a promising environmentally friendly approach for eliminating MBD from the aqueous solution that is also cost-effective. This technology could be useful in addressing the rising demand for adsorbents employed in environmental protection processes.

Structural and Adsorptive Characteristics of 2D Multilayer Nanoflakes of NiCo Phosphates for Chromium(VI) Removal: Experimental and Monte Carlo Simulations.

Metal phosphates are efficient adsorbent materials for heavy elements present in industrial effluents because of their promising properties. Hexachromium ions are among the most dangerous contaminants owing to their harmful properties and non-degradability. Accordingly, the present work offers a simplified study of the preparation of bimetallic phosphate materials from nickel cobalt phosphate (NiCo-Ph) based on the sol–gel method in an equimolar ratio. Characterization of the bulk, crystal phase, texture profile, and nanosize of NiCo-Ph was carried out using various techniques such as Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, nitrogen adsorption–desorption isotherm measurements, field emission scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy. In this regard, the adsorption performance of NiCo-Ph was exemplified through six batch experiments, elucidating the impacts of the sorbent dose, initial concentration of pollutants, sorption time, temperature, pH, and shaking rate. According to UV/vis spectrophotometry measurements and their related calculations of NiCo-Ph, the maximum removal efficiency (RE %) of 92% and adsorption capacity (qm) of 37 mg/g were achieved at pH = 6, a dose of 5.0 g/L, 100 mg/L of [Cr(VI)], 300 rpm, adsorption time of 60 min, and 298 K. Monte Carlo simulations were also carried out to correlate the experimental data with theoretical calculations that provided a higher negative value (−911.62 kcal mol–1) for the adsorption energy of Cr(VI) in acidic medium. The adsorbent NiCo-Ph prepared by this direct method is therefore recommended for the quantification of Cr(VI) under slightly acidic solutions and at room temperature, which can maintain its efficiency even up to six cycles.

Post-modification of Uio-66-NH2 based on Schiff-base reaction for removal of Hg2+ from aqueous solution: Synthesis, adsorption performance and mechanism

A novel composite adsorbent, Uio-66-NH2/AHMP, was successfully synthesized by post-modifying Uio-66-NH2 with 6-amino-4-hydroxy-2-mercaptopyrimidine based on the Schiff-base reaction and applied to remove Hg2+ from aqueous solution. The Uio-66-NH2/AHMP was characterized by Field emission scanning electron microscopy (FE-SEM), X-ray diffractometer (XRD), Fourier transform infrared (FT-IR), X-ray photoelectron spectroscopy (XPS) and Brunner Emmet Teller (BET). The characterization results shown that sulfur/nitrogen/oxygen-containing groups were successfully introduced on the zirconium-based MOF, and that the pore structure of Uio-66-NH2/AHMP mainly contains mesopores. Subsequently, the adsorption and regeneration performance of composite Uio-66-NH2/AHMP were investigated by batch experiments, the effect of solution pH, sorbent dose, reaction time, initial Hg2+ concentration, and coexisting metal ions on the removal performance of Hg2+ were evaluated. The pH value of solution determined the charge distribution on the adsorbent surface and the form of Hg2+in aqueous solution based on experimental results and zeta potential analysis. The obtained equilibrium time and maximum adsorption capacity were 60 min and 232.5 mg/g at pH 6, 298 K, respectively. The adsorption process of Hg2+ was consistent with the pseudo-second-order kinetic and the Langmuir model. The results of regeneration studies shown that the removal efficiency of 79.2 % could be obtained after four adsorption–desorption cycles. Besides, Uio-66-NH2/AHMP exhibited excellent adsorption selectivity for Hg2+. XPS analysis indicated that the removal process was dominated by chelation between Hg2+ and nitrogen/sulfur/oxygen-containing groups. This work indicates that the Uio-66-NH2/AHMP has a good application prospect in the removal of Hg2+ from aqueous solution.

Modeling and Optimization of Heavy Metals Biosorption by Low-Cost Sorbents Using Response Surface Methodology

This paper exploits, through modeling and optimization, the experimental laboratory data on the biosorption of heavy metal ions Pb(II), Cd(II), and Zn(II) from aqueous media using soybean and soybean waste biomasses. The biosorption modeling was performed using the Response Surface Methodology, followed by optimization based on numerical methods. The aim of the modeling was to establish the most probable mathematical relationship between the dependent variables (the biosorption efficiency of the biosorbents when adsorbing metal ions, R(%), and the biosorption capacity of sorbents, q(mg/g)) and the process parameters (pH; sorbent dose, DS (g/L); initial metal ion concentration in solution, c0 (mg/L); contact time, tc (min); temperature, T (°C)), validated by methodologies specific to the multiple regression analysis. Afterward, sets of solutions were obtained through optimization that correlate various values of the process parameters to maximize the objective function. These solutions also confirmed the performance of soybean waste biomass in the removal of heavy metal ions from polluted aqueous effluents. The results were validated experimentally.

Effect of nano bentonite on direct yellow 50 dye removal; Adsorption isotherm, kinetic analysis, and thermodynamic behavior

Developing countries suffering from the toxicity of different industrial effluents especially dyes. This study successfully prepared and characterized nano-bentonite for anionic dye removal (DY 50). The prepared nanoparticles were characterized by X-Ray Diffraction (XRD), X-ray Fluorescence (XRF), Scanning Electron Microscope (SEM), EDAX analysis, FT-IR, and TGA and the obtained results indicated the formation of nanoparticles with an average size of 15 nm. The effect of different operating conditions was studied using different pH, dose, contact time, temperature, and initial DY 50 concentrations. The obtained results indicated that nano bentonite was able to adsorb about 78.3 and 100% for initial concentrations of 100±8.1 and 20 ±1.62 mg/L, respectively. The optimum removal conditions were observed at acidic media (pH 3) using sorbent material dosage 1 g/L for 45 min and 30°C. The adsorption isotherm, kinetic analysis, and thermodynamic behavior were studied by using linear equation form, and the adjusted R2 was compared to detect the preferred models. The adsorption isotherm indicated that heterogeneous, as well as multilayer adsorption, plays an important role in the removal of dye. Kinetic studies indicated the chemisorption interaction between sorbed and adsorbed molecules. Thermodynamic behavior indicated the reaction is exothermic with ∆H equal to −5.24 KJ/mol and ∆S equal −74.2 J/K.mol. Finally, this study strongly recommended using nano bentonite for DY 50 removal from an aqueous solution. The RSM relations show significant relations in all removal models with p-value <0.001. The ANN results indicated that the most effective operating conditions are the effect of nano bentonite dose followed by the pH effect.

New fabrication of CuFe2O4/PAMAM nanocomposites by an efficient removal performance for organic dyes: Kinetic study.

Today, removing pollutants from water sources is essential because of the population increase and the growing need for safe drinking water. Dyes are one of the most critical pollutants from industrial effluents such as paper and textile industries that profoundly affect the environment. There are several ways to remove environmental contaminants. Magnetic nanoparticles have a high ability to adsorb dyes. Of course, increasing the interaction between magnetic nanomaterials and pollutants is also essential, which can be done using porous materials such as dendrimers. In this work, the synthesis of CuFe2O4 magnetite nanoparticles within the polyamidoamine dendrimers structure was used as an efficient sorbent to remove both alizarin reds (ARS) and brilliant green (BG) dyes. Moreover, various parameters for dyes removal were studied. The optimum removal conditions were obtained for ARS within 30min at a sorbent dose of 2mg per 5mL for the initial dye concentration of 7.0ppm in pH 6at 25°C, and for BG within 45min at a sorbent dose of 5mg per 5mL for the initial dye concentration of 17.0ppm in pH 8at 25°C. At the optimum values of the above parameters, both dyes' removal efficiency was more than 97%. Also, the obtained results showed that the adsorption isotherm follows the Langmuir model and Temkin model for ARS and BG, respectively. This method was successfully used for the removal of both dyes in water samples.

One-Step Fabrication of Amino-Functionalized Fe3O4@SiO2 Core-Shell Magnetic Nanoparticles as a Potential Novel Platform for Removal of Cadmium (II) from Aqueous Solution

Fe3O4@SiO2-NH2 core-shell magnetic nanoparticles were developed by a rapid one-step precipitation route followed by reverse microemulsion and amine functionalization. In this study, an Fe3O4@SiO2-NH2 nanoparticle was used to evaluate its adsorption efficiency for the treatment of a synthetic solution of Cd(II) ion. The structural and physicochemical properties of Fe3O4@SiO2-NH2 nanoparticles were characterized by XRD, SEM-EDAX, TEM, FTIR and TGA. From the TEM analysis, the morphology of Fe3O4@SiO2-NH2 was found as 100–300 nm. In TGA, the first weight loss was noticed between 373 and 573 K, the second was between 673 and 773 K and the final weight loss took place above 773 K. Batch experimental tests, such as pH, dosage of Fe3O4@SiO2-NH2, Cd(II) ion concentration, temperature as well as interaction time, were conducted and evaluated. Experimental study data were used for the non-linear forms exhibited by isotherms and kinetics of the sorption procedure. The equilibrium adsorption observations were adequately combined with pseudo-first-order kinetics as well as Freundlich isotherm. Monolayer maximum adsorption capacity was found to be 40.02 mg/g, recorded at pH 6 with an interaction time of 30 min, temperature of 303 K and sorbent dose of 2.0 g/L. The thermodynamic study indicated that the adsorption process was an exothermic, spontaneous reaction (−∆oo = −15.46–7.81 (kJ/mol)). The as-synthesized sorbent had excellent recyclability, and its adsorption efficiency was maintained after five cycles of reuse. The findings of the study exhibited the magnetic Fe3O4@SiO2-NH2-nanoparticle as an alternative effective adsorbent in eradicating Cd(II) ions from aqueous solution.

Green approach for fabrication of graphene from polyethylene terephthalate (PET) bottle waste as reactive material for dyes removal from aqueous solution: Batch and continuous study

This study is concerned with the synthesis of graphene from PET waste bottles as raw material and investigates the possibility of using it as an inexpensive and active material for the removal of methylene blue (MB) and methyl orange (MO) from aqueous solution. The synthesis process was achieved in a green way through the manufacture of a stainless steel autoclave that reduces the emission of toxic gases and accelerates the pyrolysis process. The synthesized graphene is characterized by FTIR, SEM, TEM, EDX, XRD, and surface area. Many factors that affect dyes removal percent were studied such as contact time, initial pH of the solution, agitation speed, initial concentration, and sorbent dosage. The sorption isotherm and kinetics study were described using two isotherm models (Langmuir and Freundlich) and two kinetic models (pseudo-first-order and pseudo-second-order), while the column experimental data were fitted with four breakthrough curve models (Thomas-BDST, Bohart–Adams, Yan, and Clark). The experimental results proved that the prepared graphene can be a promising reactive material for the removal of dyes (MB and MO) from aqueous solutions.

Synergistic removal of tetracycline and copper (II) by in-situ B-Fe/Ni nanocomposite—A novel and an environmentally sustainable green nanomaterial

Since both antibiotics and heavy metals are regular entities in aquatic environments nowadays, finding an effective strategy for simultaneous removal of both the contaminants has gained importance. In this work clay supported Fe/Ni (B-Fe/Ni) nanocomposite was prepared through an in-situ green synthesis approach and characterized by SEM-EDX, FTIR, XRD, and XPS to confirm the size, surface functional groups, and elemental composition of the composite. The adsorbent was then utilized for simultaneous removal of TC and Cu 2 + from aqueous solutions in single and binary modes. In a single system, the B-Fe/Ni (sorbent dosage 1000 mg/L, pH7, TC conc. 60 mg/L, and Cu conc. 1 mg/L) removed 96% and 83% of TC and Cu 2 + , respectively, while in a binary mode more than 90% of TC and 80% of Cu 2 + were removed. This enhanced adsorption efficiency is attributed to the complex formation through TC–Cu 2 + bridging and greater affinity of the adsorbent for the TC–Cu 2 + complex than TC or Cu 2 + individually. TC and Cu 2 + were adsorbed to the surface of B-Fe/Ni, and Fe 0 in B-Fe/Ni reduced Cu 2 + to Cu 0 and degraded TC to the smaller molecules. The existence of Fe (II) and Fe (III) in the B-Fe/Ni complexed with the amide of TC and Cu(II) which was confirmed by XPS and FTIR analysis. The reusability study revealed that the TC and Cu 2 + removal efficiency was above 60% for TC and 50% for Cu 2 + till the third cycle, and validation with the real water samples confirmed above 75% TC and Cu 2 + removal. The residual toxicity of B-Fe/Ni interacted TC-Cu 2 + solution in freshwater Scenedesmus sp . was significantly lower compared to the untreated one, indicating that the process effectively reduced the environmental toxicity of the pollutants. • A novel green In-situ B-Fe/Ni nanocomposite prepared. • B-Fe/Ni showed exceptional removal capacity for TC 96±0.5% and for Cu 2+ 83±0.8% • TC–Cu 2+ complex creates a bridge between the adsorbent and the adsorbate. • Adsorption and oxidation–reduction responsible for elimination of TC and Cu 2+

Factors influencing sorption of trace elements in contaminated waters onto ground nut shells

Biosorbent materials such as nut shells has been considered a promising alternative to the classic methods to remove potentially toxic elements from contaminated waters, improving water quality for other uses. The present study evaluated the sorption capacity of almond, hazelnut, pistachio and walnut shells for the single and simultaneous removal of As, Cd, Co, Hg, Ni, Pb and Zn from contaminated waters. The influence of key parameters such as sorbent dose, ionic strength (ultrapure water vs. mineral water), element competition (mono-vs. multi-element spiked solution) and initial element concentration (maximum allowed value in wastewater discharges and ten times lower) was assessed. Hazelnut shells stood out as the material with higher potential to remove Cd, Co, Hg, Ni, Pb and Zn in the tested conditions, achieving up to 99% of removal (Cd and Pb). Arsenic was not removed by none of the studied materials and the removal of Cr was only obtained in a simple matrix and in mono-element solution (41% of removal). An increase of matrix complexity negatively affected the sorption capacity of all the biosorbents in the removal of all the elements tested. The same behavior was obtained when the elements were simultaneously present in solution, with Pb, Cd and Hg being highly influenced by the presence of other elements. The increase in sorbent dose from 1 to 5 g/L allowed to at least duplicate the removal of Cd, Co, Ni and Zn by all the biosorbents. When decreasing the initial element concentration ten times the maximum allowed value in wastewater discharges, a significant increase of elements removal was attained, more pronounced for Hg and Pb. The possibility to change initial conditions towards high efficiencies validate the high potential of those biosorbents to be used in water remediation, with special focus on hazelnut shells, although other sorbents such as walnut or almond shells can be considered efficient with appropriate initial conditions and depending on the target elements to be removed.

Bipyridine containing poly(amic-acid)s: Synthesis, characterization, and sorption behavior toward the Ni (II) ions

New poly(amic-acid)s sorbents, bearing bipyridine chelating groups, were synthesized by reaction of benzophenonetetracarboxylic dianhydride (BTDA) with different percentages of 4,6-bis(4-aminophenyl)-2,2′-bipyridine (BAPB), and 1,4-phenylene diamine (PPD) and were characterized by FTIR and 1HNMR spectroscopies. Because of the imidization of these poly(amic-acid)s after about 10% weight loss, their thermal stability was raised to about 500°C. The glass transition temperatures of these polymers were in the range of 154–166°C. The sorption of Ni(II) by these sorbents from the aqueous solutions was investigated by varying different parameters such as the contact time, pH, and sorbent dosage. Results indicated that the optimum efficiencies of these sorbents toward Ni(II) were at 25°C, at pH = 4 and after about 75 min. According to the Langmuir equation, the maximum uptake capacity ( qm) of PAA30/70 as a best sorbent for nickel was 14.66 mg.g−1. The modeling results confirmed the pseudo-second-order sorption for the metal ion. The morphology of these sorbents before and after sorption of Ni(II) was investigated using Scanning Electron Microscopy and the results confirmed the porous structure of these sorbents. [Formula: see text]

Potential of Moringa Oleifera Seed as a Natural Adsorbent for Wastewater Treatment

The present study deals with the appropriateness of the coagulation process using natural coagulant Moringa oleifera seed. Natural coagulants are useful for the treatment of wastewater because of its sustainability, cost-effectiveness, non-toxicity and lesser quantity of sludge formation. M. oleifera seed having a chemical composition of polypeptides having 6 amino acids like arginine acid, methionine acid, glutamic acid, phenylalanine, threonine, and histidine. M. oleifera is also known as a cationic polyelectrolyte and having molecular weight 6,000 to16,000 Dalton. The main objective of research work is the application of the M. oleifera seed as a natural adsorbent to treat synthetic dairy wastewater. The effects of pH, agitation time, the dose of sorbent and efficacy of M. oleifera seeds kernel for turbidity removal was assessed. M. oleifera seed eliminates turbidity 95 % and colour 94 % using 0.22 gm pod powder, and 0.2 L of 1.0 g/L synthetic dairy wastewater. Naturally dried M. oleifera seeds remove turbidity 95 %, sundried seeds remove turbidity 52 % and oven-dried seeds 45 %. As naturally dried M. oleifera pod having more surface area for adsorption and inter-particulate bridging which extract the extra active ingredients. pH range between 5 and 8 is more suitable to degrade the turbidity and colour. It is concluded that in the presence of an aqueous soluble cationic coagulant protein has great potential to remove the turbidity and colour of wastewater.
 HIGHLIGHTS
 
 oleifera seed having a chemical composition of polypeptides having 6 amino acids like arginine acid, methionine acid, glutamic acid, phenylalanine, threonine, and histidine
 oleifera seeds consist of crude fiber, lignin, hemicellulose, and cellulose. It also contains amino functional groups (R-NH3), carboxyl group (C=O), and fiber carbonaceous. The functional group present in M. oleifera seeds is dissociated during the adsorption process at various pH
 oleifera has good property of coagulation-flocculation (C-F)
 The effectiveness of naturally dried seed kernel is more effective than other seed kernels
 
 GRAPHICAL ABSTRACT

Sequential recovery of Cu(II), Cr(III), and Zn(II) from electroplating sludge leaching solution by an on-line biosorption method with dosage controlling

Hydrometallurgy leaching is a common method used to recycle heavy metals from electroplating sludge, but the subsequent separation of heavy metals from the complex leaching solution is difficult. In this study, Cu(II), Zn(II), and Cr(III) were sequentially recycled from electroplating sludge by an on-line biosorption method with dosage controlling. The results showed that the three metals mainly existed in their labile forms and could be leached by HNO3. A series of amine-modified bagasse biosorbents were prepared, and diethylenetriamine-modified sorbent was chosen and fixed in a column to remove heavy metals from the leaching solution. Sorbent dosage experiments showed Cu(II) was recycled exclusively at a dosage of 1.5 g/L, while Zn(II) and Cr(III) were recycled simultaneously at a dosage of 3.8 g/L when treating 800 mL of a leaching agent containing 13.4, 9.9, and 7.1 mg/L of Cu, Zn, and Cr. A linear relationship between the dosage and amount of adsorbed metal ions was obtained. The XPS results illustrated that the column had an adsorption affinity order of Cu(II)>Zn(II), Cr(III)≫Ca(II), Mg(II). Cu(II) was enriched in the foot layer, and Zn(II) and Cr(III) were enriched in the middle layer of the column, while co-ions could not be absorbed. According to these results, Cu(II), Zn(II), and Cr(III) could be sequentially recycled by using these columns in-series.

Removal of Chromium (VI) and Lead (II) from Aqueous Solution Using Domestic Rice Husk Ash- (RHA-) Based Zeolite Faujasite

Rice husk ash (RHA), is a widely available biobased source for high purity silica. In this work, zeolite Faujasite (FAU) is synthesized using extracted silica from RHA (collected from a local region of Bangladesh). The synthesized zeolite FAU was used as an adsorbent for Cr(VI) and Pb (II) batch-wise adsorptive removal from respective aqueous solution. The synthesized zeolite FAU was characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen-sorption, and Fourier transfer infrared (FT-IR) spectroscopy. Metal ion adsorption studies were performed by varying metal concentration (20–100 mg/L for Cr(VI) and 900–133 mg/L for Pb(II)), sorbent dosage (2–10 g/L for chromium and 0.5–1.5 g/L for lead), and contact time (10–120 min for both metal ions). The maximum adsorption capacity of RHA-based zeolite FAU was found to be 3.56 mg/g and 342.16 mg/g for Cr(VI) and Pb(II), respectively. Since the sorption data was found to match with Langmuir isotherm, a monolayer adsorption was occurred. The regeneration of the RHA-based zeolite FAU by NaCl solution showed the potential of repeated as well as continuous operation.

A Facile Review on the Sorption of Heavy Metals and Dyes Using Bionanocomposites

Presently, hazardous metal and dye removal from wastewater is one of the major areas of research focus. For the elimination of these contaminants, many approaches have been devised and applied. However, the accomplishment of various water treatment processes has largely depended on the medium utilized and the associated problem with the leaching of harmful compounds into the water process with most commercial and chemically manufactured materials for water treatment processes. Hence, this study is aimed at reviewing existing studies on the sorption of heavy metals (HMs) and dyes using bionanocomposites (BNCs). The key focus of this review is on the development of eco-friendly, effective, and appropriate nanoadsorbents that could accomplish superior and enhanced contaminant sequestration using BNCs owing to their biodegradability, biocompatible, environmentally friendly, and not posing as secondary waste to the environment. The sorption of most pollutants was observed to be pH, sorbent dosage, and initial contaminant concentration-dependent, with most contaminants’ elimination taking place in the pH range of 2-10. The sorption process of HMs and dyes to various BNCs was superlatively depicted utilizing the Langmuir (LNR) and Freundlich (FL) as well as the pseudo-second-order (PSO) models, suggestive of the sorption process of a monolayer and multilayer and the chemisorption process, the rate-limiting stage in surface sorption. The established sorption capacities for the reviewed sorption process for various contaminants ranged from 1.47 to 740.97 mg/g. Future prospective for the treatment and remediation of contaminated water using BNCs was also discussed.