Optimizing adsorptive removal of malachite green and methyl orange dyes from simulated wastewater by Mn‐doped CuO‐Nanoparticles loaded on activated carbon using CCD‐RSM: Mechanism,regeneration, isotherm,kinetic, and thermodynamic studies

In the present work, Mn‐doped CuO‐NPs‐AC was prepared by a simple method, characterized using various techniques such as FESEM, EDX, XRD, PSD, and pH_pzc and finally used for the adsorption of malachite green (MG) and methyl orange (MO) in a number of single and binary solutions. A series of adsorption experiments were conducted to investigate and optimize the influence of various factors (such as different pH, concentration of MG and MO, adsorbent mass, and sonication time) on the simultaneous adsorption of MG and MO using response surface methodology. Under optimal conditions of pH 10, adsorbent dose of 0.02 g, MG concentration of 30 mg L^?1, MO concentration of 30 mg L^?1, and sonication time of 4.5 min at room temperature, the maximum predicted adsorption was observed to be 100.0%, for both MG and MO, showing that there is a favorable harmony between the experimental data and model predictions. The adsorption isotherm of MO and MG by Mn‐doped CuO‐NPs‐AC could be well clarified by the Langmuir model with maximum adsorption capacity of 320.69 mg g^?1 and 290.11 mg g^?1 in the single solution and 233.02 mg g^?1 and 205.53 mg g^?1 in the binary solution by 0.005 g of adsorbent mass for MG and MO, respectively. Kinetic studies also revealed that both MG and MO adsorption were better defined by the pseudo‐second order model for both solutions. In addition, the thermodynamic constant studies disclosed that the adsorption of MG and MO was likely to be influenced by a physisorption mechanism. Eventually, the reusability of the Mn‐doped CuO‐NPs‐AC after six times showed a reduction in the adsorption percentage of MG and MO.     

Yolk–shell microspheres assembled from Preyssler‐type NaP5W30O11014− polyoxometalate and MIL‐101(Cr) metal–organic framework: A new inorganic–organic nanohybrid for fast and selective removal of cationic organic dyes from aqueous media

Novel inorganic–organic yolk–shell microspheres based on Preyssler‐type NaP₅W₃₀O₁₁₀^14? polyoxometalate and MIL‐101(Cr) metal–organic framework (P₅W₃₀/MIL‐101(Cr)) were synthesized by reaction of K_12.5Na_1.5[NaP₅W₃₀O₁₁₀], Cr(NO₃)₃·9H₂O and terephthalic acid under hydrothermal conditions at 200°C for 24 h. The as‐prepared yolk–shell microspheres were fully characterized using various techniques. All analyses confirmed the incorporation of the Preyssler‐type NaP₅W₃₀O₁₁₀^14? polyoxometalate into the three‐dimensional porous MIL‐101(Cr) metal–organic framework. The results revealed that P₅W₃₀/MIL‐101(Cr) demonstrated rapid adsorption of cationic methylene blue (MB) and rhodamine B (RhB) with ultrahigh efficiency and capacity, as well as achieving rapid and highly selective adsorption of MB from MB/MO (MO = methyl orange), MB/RhB and MB/RhB/MO mixtures. The P₅W₃₀/MIL‐101(Cr) adsorbent not only exhibited a high adsorption capacity of 212 mg g^?1, but also could quickly remove 100% of MB from a dye solution of 50 mg l^?1 within 8 min. The effects of some key parameters such as adsorbent dosage, initial dye concentration and initial pH on dye adsorption were investigated in detail. The equilibrium adsorption data were better fitted by the Langmuir isotherm. The adsorption kinetics was well modelled using a pseudo‐second‐order model. Also, the inorganic–organic hybrid yolk–shell microspheres could be easily separated from the reaction system and reused up to four times without any change in structure or adsorption ability. The stability and robustness of the adsorbent were confirmed using various techniques.     

Synthesis and characterization of SnO2/(NH4)2‐SnCl6 nanocomposites loaded on activated carbon and its application for adsorption of methylene Blue and Orange G

The present study deals with the synthesis and characterization (FE‐SEM, particle size distribution, XRD and point of zero charge) SnO₂/(NH₄)₂‐SnCl₆ nanocomposites loaded on activated carbon (SnO₂/(NH₄)₂‐SnCl₆‐NCs‐AC) and its subsequent application for the simultaneous removal of Methylene Blue (MB) and Orange G (OG) from aqueous solution. Response surface methodology (RSM) based on central composite design (CCD) give trend of influencing responses with respect to five parameters such as contact time (X₁), OG concentration (X₂), MB concentration (X₃), adsorbent mass (X₄) and pH (X₅). In later stage following recognition of significant variables and interaction, quadratic model generated which are able to predict the dyes removal in different conditions. Justification and selection of significant terms was conducted based on analysis of variance and Fisher's F‐test Optimal value of contact time, OG concentration, MB concentration, adsorbent mass and pH were set at 4.0 min, 10 mg l^?1, 20 mg L^?1, 0.015 g and 6.0, respectively, which lead to achievement of best experiment removal percentage of 97.0 and 99.5% OG and MB respectively, from their binary solutions. The whole experimental data follow pseudo‐first‐order and pseudo‐second‐order rate equations. The fitting experimental data to more available conventional model like Langmuir, Freundlich, Temkin and Dubinin‐Radushkevich isotherm models revel more ability of Langmuir model (with R² > 0.997) for explanation of system in equilibrium. The adsorption efficiency remained high even after the five cycle of reuse (99.76% and 95.56% for MB and OG, respectively).     

Selective and sensitive determination of silver ions at trace levels based on ultrasonic‐assisted dispersive solid‐phase extraction using ion‐imprinted polymer nanoparticles

We describe ultrasonic‐assisted dispersive solid‐phase extraction based on ion‐imprinted polymer (UA‐DSPE‐IIP) nanoparticles for the selective extraction of silver ions. Ultrasound is a good and robust method to facilitate the extraction of target ions in the sorption step and elution of the target ions in the desorption step. The IIP nanoparticles used in the UA‐DSPE‐IIP were prepared by precipitation polymerization. To prepare the IIP nanoparticles, 2‐vinylpyridine, ethylene glycol dimethacrylate, 2,2′‐azobisisobutyronitrile, 2‐picolinic acid, silver and chloroform–methanol (50:50) solution were used as functional monomer, cross‐linker, initiator, silver‐binding ligand, template ion and porogen, respectively. The IIP nanoparticles were characterized using Fourier transformed infrared spectroscopy, thermogravimetric and differential thermal analysis, X‐ray diffraction and scanning electron microscopy. A Box–Behnken design was used for optimization of sorption and desorption steps in UA‐DSPE‐IIP. In the sorption step: pH of solution, IIP amount (mg), sonication time for sorption (min); in the desorption step: concentration of eluent (mol l⁻¹), volume of eluent (ml), sonication time (min) for desorption were investigated and optimized by Box–Behnken design. The optimum conditions for the method were: pH of solution, 7; sonication time for sorption, 7 min; IIP amount, 17 mg; type and concentration of eluent, HCl 1.5 mol l⁻¹; volume of eluent, 2 ml; sonication time for desorption, 140 s. Under the optimized conditions the limit of detection and relative standard deviation for the detection of silver ions using UA‐DSPE‐IIP were found to be 0.09 μg l⁻¹ and <3%, respectively.     

Mixed phase Fe2O3/Mn3O4 magnetic nanocomposite for enhanced adsorption of methyl orange dye: Neural network modeling and response surface methodology optimization

In this research, a novel magnetic mesoporous adsorbent with mixed phase of Fe₂O₃/Mn₃O₄ nanocomposite was prepared by a facile precipitating method and characterized extensively. The prepared nanocomposite was used as adsorbent for toxic methyl orange (MO) dye removal from aqua matrix considering its high surface area (178.27 m²/g) with high saturation magnetization (23.07 emu/g). Maximum dye adsorption occurs at solution pH 2.0 and the electrostatic attraction between anionic form of MO dye molecules and the positively charged nanocomposite surface is the main driving force behind this adsorption. Response surface methodology (RSM) was used for optimizing the process variables and maximum MO removal of 97.67% is obtained at optimum experimental condition with contact time, adsorbent dose and initial MO dye concentration of 45 min, 0.87 g/l and 116 mg/l, respectively. Artificial neural network (ANN) model with optimum topology of 3–5–1 was developed for predicting the MO removal (%), which has shown higher predictive ability than RSM model. Maximum adsorption capacity of this nanocomposite was found to be 322.58 mg/g from Langmuir isotherm model. Kinetic studies reveal the applicability of second‐order kinetic model with contribution of intra‐particle diffusion in this process.     

Synthesis of CuS nanoparticles loaded on activated carbon composite for ultrasound‐assisted adsorption removal of dye pollutants: Process optimization using CCD‐RSM,equilibrium and kinetic studies

In this study, the CuS nanoparticles loaded on activated carbon (CuS‐NPs‐AC) composite was synthesized and then, characterized by XRD and FE‐SEM analyses. The prepared composite was used as a potential adsorbent for the simultaneous ultrasound‐assisted removal of Indigo Carmine (IC) and Safranin‐O (SO). The CuS‐NPs‐AC dose (0.01‐0.03 g), sonication time (1‐5 min), initial SO concentration (5‐15 mg L^‐1) and initial IC concentration (5‐15 mg L^‐1) as expectable effective parameters were studied by central composite design (CCD) under response surface methodology (RSM) to obtain an useful knowledge about the effect of simultaneous interaction between IC and SO on their removal percentage. The optimum SO and IC removal percentages were determined to be 98.24 and 97.15% at pH = 6, 0.03 g of the CuS‐NPs‐AC, 3 min sonication time, 12 and 10 mg L^‐1 of IC and SO. The values of coefficient of determination (R²) for SO and IC were 0.9608 and 0.9796, respectively, indicating the favorable fitness of the experimental data to the second order polynomial regression model. The isotherm data were well correlated with Freundlich model. The maximum monolayer adsorption capacities of 87.5 and 69.90 mg g^‐1 at room temperature for IC and SO in the investigated binary system expressed the high efficiency of the novel adsorbent for water cleanup within a short time. The investigation of correlation between time and rate of adsorption revealed that IC and SO adsorption onto the CuS‐NPs‐AC followed pseudo‐second‐order and intra‐particle diffusion simultaneously.     

Preparation and characterization of novel bi-functionalized xerogel for removal of methylene blue and lead ions from aqueous solution in batch and fixed-bed modes: RSM optimization,kinetic and equilibrium studies

A new bi-functionalized xerogel is fabricated and then was identified by ²⁹Si CP MAS NMR, SEM, FTIR, and nitrogen adsorption–desorption approaches. As-prepared xerogel efficiency for simultaneous uptake of methylene blue (MB) and Pb²⁺ ions from aqueous solution is investigated. Individual and combination effects of operating variables (xerogel mass, contact time and initial MB and Pb²⁺ ion concentration) on the retention performance is achieved with central composite design (CCD) and upgraded through response surface method (RSM). Batch equilibrium outcomes uncovered that MB and Pb²⁺ ions adsorption onto hybrid composite could be all around depicted by Langmuir isotherm model contrasted with Freundlich equation. Howbeit, the column trials reported that the breakthrough capacities of MB and Pb(II) are observed to be 512 mg.g⁻¹ and 400 mg.g⁻¹ respectively. XPS and FTIR investigations uncovered that the main mechanism of lead uptake ought to be credited to the chelation with –NH₂ and ion exchange with –SH groups in the xerogel frameworks. While the MB adsorption system is proposed to be electrostatic attractions, π-π stacking interactions and hydrogen bonds. The work undertaken in this research highlights the major role of the as-synthesized xerogel for treatment of industrial wastewater.     

Multi‐responses optimization of simultaneous adsorption of methylene blue and malachite green dyes in binary aqueous system onto Ni:FeO(OH)‐NWs‐AC using experimental design: derivative spectrophotometry method

In this research, response surface methodology (RSM) approach using Central Composite Design (CCD) coupled by derivative spectrophotometry method was applied to develop mathematical model and optimize process parameters for simultaneous adsorption of methylene blue (MB) and malachite green (MG) from aqueous solution using Ni:FeO(OH) ‐ NWs‐AC. The optimal conditions to adsorption of MB and MG in binary mixture solution from aqueous solution were found at pH 8.0, MB concentration 20 mg L^‐1, MG concentration 20 mg L^‐1, adsorbent dosage 0.033 g and contact time 40 min. At these conditions, high adsorption efficiency (99.39% and 100.0% for MB and MG, respectively) was achieved. Among experimental equilibrium, Langmuir isotherm model fitted well with maximum monolayer adsorption capacity of 28.6 and 29.8 mg g^‐1 for MB and MG, respectively. The adsorption kinetic data followed pseudo second‐order kinetics for MB and MG dyes.     

Synthesis and characterization of antibacterial chromium iron oxide nanoparticle‐loaded activated carbon for ultrasound‐assisted wastewater treatment

The aim of this study was to evaluate the surface adsorption capacity of CrFeO₃ nanoparticle‐loaded activated carbon (CrFeO₃‐NPs–AC) for the removal of a cationic dye (methyl violet, MV). CrFeO₃‐NPs were hydrothermally synthesized and loaded on AC followed by characterization using X‐ray diffraction, field‐emission scanning electron microscopy and energy‐dispersive and Fourier transform infrared spectroscopies. The CrFeO₃‐NPs were tested for in vitro antibacterial activities against Gram‐positive (Staphylococcus aureus) and Gram‐negative (Pseudomonas aeruginosa) bacteria. Minimum inhibitory and minimum bactericidal concentrations of CrFeO₃‐NPs–AC were obtained to be 50 and 100 μg ml^?1, respectively, against S. aureus and 25 and 50 μg ml^?1 against P. aeruginosa. These results indicated the antibacterial properties of CrFeO₃‐NPs–AC. To investigate the adsorption process, several systematic experiments were designed by varying parameters such as adsorbent mass, pH, initial MV concentration and sonication time. The adsorption process was modelled and the optimal conditions were determined to be 0.013 g, 7.4, 15 mg l^?1 and 8 min for adsorbent mass, pH, MV concentration and sonication time, respectively. The real experimental data were found to be efficiently explained by response surface methodology and genetic algorithm model. Kinetic studies for MV adsorption showed rapid sorption dynamics described by a second‐order kinetic model, suggesting a chemisorption mechanism. Then, the experimental equilibrium data obtained at various concentrations of MV and adsorbent masses were fitted to conventional Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. Dye adsorption equilibrium data were fitted well to the Langmuir isotherm. From the Langmuir model, the maximum monolayer capacity was calculated to be 65.67 mg g^?1 at optimum adsorbent mass.     

Fabrication and optimization calix[8]arene-PbS nanoadsorbents for the adsorption of methylene blue: Isotherms,kinetics and thermodynamics studies

The present study aims to determine the adsorption behaviour of methylene blue (MB) dye based on calix[8]arene-modified lead sulphide (PbS) nanoadsorbents under optimal conditions. Response surface methodology (RSM) was executed to evaluate the interactive effect of three factors (adsorbent dosage, contact time, and pH) on the adsorption of MB dye using a central composite design (CCD). The optimised values for adsorbent dosage, contact time, and pH solution were found to be 45.00 mg of calix[8]arene-modified PbS, contact time of 180 min, and pH 6. This study reports the results of batch adsorption experiments, which include the adsorption capacity, kinetics, and isotherm of the MB adsorption process. Pseudo-first order and pseudo-second order were demonstrated for their quality to fit the data. Pseudo-second order was the best in fitting the adsorption data with the higher R² values (R² > 0.928), indicating chemisorption to be the mechanism of adsorption. The Langmuir and Freundlich equilibrium models were employed to determine the isotherm parameters. The equilibrium assessment illustrated that the Langmuir isotherm model fitted well with the adsorption data, and a maximum MB adsorption capacity of 11.90 mg/g was achieved. The characterisation studies with EDX, FESEM, and FTIR indicated a successful synthesis of calix[8]arene-modified PbS.     

An easily organic–inorganic hybrid optical sensor based on dithizone impregnation on mesoporous SBA‐15 for simultaneous detection and removal of Pb(II) ions from water samples: Response‐surface methodology

In this study, a novel organic–inorganic hybrid adsorbent for single‐step detection and removal of Pb(II) ions based on dithizone (DZ) anchored on mesoporous SBA‐15 was fabricated. The designed solid optical sensor revealed rapid colorimetric responses and high selectivity. Central composite design (CCD) combined with desirability function (DF) was applied to evaluate the interactive effects and optimization of important variables such as pH value, mesoporous SBA‐15 dosage, contact time and initial concentration of Pb(II) ions and optimum conditions for each of the factors were obtained 6.0, 25 mg, 30 min and 20 μg ml^{− 1}, respectively. This adsorbent or solid optical chemo sensor exhibited a linear range of 1.0 to 100.0 μg ml⁻¹ of Pb(II) ion concentration with a detection limit of 0.07 μg ml⁻¹. This adsorbent was applied to determine and remove the Pb(II) in spiked samples. Various isotherm models such as Langmuir, Freundlich, Temkin and Dubinin–Radushkevich were studied for fitting the experimental equilibrium data. Langmuir model was chosen as an efficient model. Various kinetic models such as pseudo‐first, second order intraparticle, diffusion models were studied for analysis of experimental adsorption data and the pseudo second order model was chosen as an efficient model.     

Facile synthesis of magnetic hybrid metal–organic frameworks with high adsorption capacity for methylene blue

A magnetic hybrid material (Fe₃O₄‐COOH/HKUST‐1) was easily synthesized via a two‐step simple solvothermal method. Through adding sodium acrylate directly into the synthesis of Fe₃O₄ spheres, the surface has more carboxyl groups. It is notable that the reactions proceed without use of organic surfactants. The magnetic hybrid material was characterized using various techniques. The magnetic hybrid material has a high specific surface area (430.15 m² g⁻¹) and excellent magnetism (23.65 emu g⁻¹). It is an efficient adsorbent for removing organic dyes like methylene blue (MB) from aqueous solution. It also can be easily recovered from liquid media using an external magnetic field. Adsorption experiment shows the magnetic hybrid material possesses a high adsorption capacity (118.6 mg g⁻¹), and has high adsorption efficiency (94.3%) after five adsorption cycles with ethanol (0.2% HCl) as eluent. The sorption kinetics and isotherm analysis indicate these sorption processes are better fitted to the pseudo‐second‐order and Langmuir equations. Thermodynamic study shows the sorption processes are spontaneous and endothermic.     

Phosphate uptake behavior and mechanism analysis of facilely synthesized nanocrystalline Zn‐Fe layered double hydroxide with chloride intercalation

Zn‐Fe layered double hydroxide with chloride intercalation (ZFCL) was synthesized by a coprecipitation method at room temperature. ZFCL was characterized by N₂ adsorption‐desorption isotherms, X‐ray diffraction, scanning electron microscope, Zeta‐sizer analyzer, X‐ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. The results showed that ZFCL had large surface area and layered structure. The maximum adsorption capacity of ZFCL was 150.6 mg/g at 25°C. That was higher than most other adsorbent which were reported. The kinetic data were described better by the pseudo‐second‐order adsorption kinetic rate model. The adsorption isotherm on the adsorbent was described by Langmuir, Freundlich, and Sips models at pH 6 and followed the fitting order: Sips >Freundlich>Langmuir. Thermodynamic analyses indicated that the phosphate adsorption on ZFCL was endothermic and spontaneous in nature. The sequence of coexisting cations and anions competing with phosphate was Ca²⁺ > Mg²⁺ > Na⁺ and SO₄²⁻ > NO₃⁻ > Cl⁻. ZFCL can be regenerated by the sequential use of NaOH and ZnCl₂. The adsorption capacity remained high as 108.6 mg/g after regeneration of 3 times. The results of zeta potential, Fourier transform infrared spectroscopy, and X‐ray photoelectron spectroscopy analyses indicated that the phosphate adsorption mechanisms involved ion exchange, Zn₃(PO₄)₂ precipitation, and the formation of inner‐sphere complex via replacement of surface hydroxyl groups by phosphate.     

Efficient removal of MB dye using litchi leaves powder adsorbent: Isotherm and kinetic studies

Removal of Methylene Blue (MB) dye using Litchi Leaves Powder (LLP) material was carried out in batch mode. Effect of the mass of the adsorbent (0.1–2.5 g/L), pH of the solution (2−12), starting concentration of MB dye (50–150 mg/L), ionic strength using NaCl (0.1–0.5 M) as an electrolyte, contact time (0–60 min) on the adsorption of MB dye was studied. To calculate pH at which LLP material surface becomes neutral point of zero charge (pH_pzc) is also determined and found to be 6.48. Removal process best fit in the pseudo-second-order kinetic model as indicated by its higher R² value (0.999). Isotherm models (Freundlich and Langmuir) were fitted to the data obtained from the experiment to understand the adsorption behaviour. Result shows that experimental data were fitted to the both isotherm models (Freundlich and Langmuir) as indicated by higher R² value for both Freundlich (0.991) and Langmuir (0.994) model, and it was determined that LLP has a maximum adsorption capacity of 119.76 mg/g.     

Synthesis of nitrogen doped activated carbon/polyaniline material for CO2 adsorption

The equilibrium adsorption isotherms of carbon dioxide and nitrogen on the nitrogen doped activated carbon (NAC) prepared by the chemical activation of a pine cone‐based char/polyaniline composite were measured using a volumetric technique. CO₂ and N₂ adsorption experiments were done at three different temperatures (298, 308, and 318 K) and pressures up to 16 bar, and correlated with the Langmuir, Freundlich, and Sips models. The Sips isotherm model presented the best fit to the experimental data. The N‐doped adsorbent showed CO₂ and N₂ adsorption capacity of 3.96 mmol·g⁻¹ and 0.86 mmol·g⁻¹, respectively, at 298 K and 1 bar. The selectivity predicted by ideal adsorbed solution theory (IAST) model was achieved 47.17 for NAC at 1 bar and y_N2 = 0.85 which is a composition similar to flue gas. The results showed that NAC adsorbent has a high CO₂‐over‐N₂ selectivity in a binary mixture. The relatively fast sorption rate of CO₂ on NAC compared to N₂ indicates the stronger affinity between CO₂ and amine groups. The isosteric heat of adsorption of CO₂ by the NAC demonstrated the physico‐chemical adsorption of CO₂ on the adsorbent surface. These data showed that prepared NAC could be successfully applied in separation of CO₂ from N₂.     

Enhanced adsorption performance of a novel Fe‐Mn‐Zr metal oxide nanocomposite adsorbent for anionic dyes from binary dye mix: Response surface optimization and neural network modeling

A novel adsorbent, Fe‐Mn‐Zr metal oxide nanocomposite was synthesized and investigated for removal of methyl orange (MO) and eosin yellow (EY) dyes from binary dye solution. The magnetic nanocomposite has shown surface area of 143.01 m²/g and saturation magnetization of 15.29 emu/g. Optimization was carried out via response surface methodology (RSM) for optimizing process variables, and optimum dye removal of 99.26% and 99.55% were obtained for MO and EY dye, respectively with contact time 62 min, adsorbent dose 0.45 g/l, initial MO concentration 11.0 mg/l, and initial EY concentration 25.0 mg/l. A feed forward back propagation neural network model has shown better prediction ability than RSM model for predicting MO and EY dye removal (%). Adsorption process strictly follows Langmuir isotherm model, and enhanced adsorption capacities of 196.07 and 175.43 mg/g were observed for MO and EY dye, respectively due to synergistic effects of physicochemical properties of trimetal oxides. Surface adsorption and pore diffusions are the mechanisms involved in the adsorption as revealed from kinetic studies.     

Simultaneous removal of Cu2+ and Cr3+ ions from aqueous solution based on Complexation with Eriochrome cyanine‐R and derivative spectrophotometric method

TiO₂ nanoparticles deposited on activated carbon (TiO₂–NP–AC) was prepared and characterized by XRD and SEM analysis. Subsequently, simultaneous ultrasound‐assisted adsorption of Cu²⁺ and Cr³⁺ ions onto TiO₂‐NPs‐AC after complexation via eriochrome cyanine R (ECR) has been investigated with UV–Vis and FAA spectrophotometer. Spectra overlapping of the ECR‐Cu and ECR‐Cr complex was resolve by derivative spectrophotometric technique. The effects of various parameters such as initial Cu²⁺ (A) and Cr³⁺ (B) ions concentrations, TiO₂‐NPs‐AC mass (C), sonication time (D) and pH (E) on the removal percentage were investigated and optimized by central composite design (CCD). The optimize conditions were set as: 4.21 min, 0.019 mg, 20.02 and 13.22 mg L^?1 and 6.63 for sonication time, TiO₂–NP–AC mass, initial Cr³⁺ and Cu²⁺ ions concentration and pH, respectively. The experimental equilibrium data fitting to Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models show that the Langmuir model is a good and suitable model for evaluation and the actual behavior of adsorption process and maximum adsorption capacity of 105.26 and 93.46 mg g^?1 were obtained for Cu²⁺ and Cr³⁺ ions, respectively. Kinetic evaluation of experimental data showed that the adsorption processes followed well pseudo second order and intraparticle diffusion models.     

Anchoring H3PW12O40 on aminopropylsilanized spinel‐type cobalt oxide (Co3O4‐SiPrNH2/H3PW12O40): A novel nanohybrid adsorbent for removing cationic organic dye pollutants from aqueous solutions

In this work, phosphotungstic acid (H₃PW₁₂O₄₀; PW₁₂) was chemically anchored on aminopropylsiloxane functionalized spherical Co₃O₄ nanoparticles (Co₃O₄–SiPrNH₂) and the resultant nanocomposite (Co₃O₄–SiPrNH₂/PW₁₂) was fully characterized. The results demonstrated successful anchoring of PW₁₂ on the surface of Co₃O₄–SiPrNH₂nanoparticles. The Co₃O₄–SiPrNH₂/PW₁₂ nanohybrid indicated a specific surface area of 42.14 m² g^?1, which was greater than that of pure PW₁₂ (ca. 5 m² g^?1). The adsorption efficiency of this novel adsorbent nanomaterial was evaluated for removing methylene blue (MB), rhodamine B (RhB) and methyl orange (MO) dyes from aqueous solutions. The hybrid nanomaterial exhibited a high adsorption rate and selective adsorptivity for the cationic MB and RhB dyes compared to those for anionic MO dye. The prepared hybrid nanomaterial removed over 98% of MB within 12 min. The effects of initial pH, contact time, adsorbent dosage, and temperature were investigated on the adsorption process. The adsorption capacity of nanohybrid for cationic MB dye was 38.46 mg g^‐1. Also, adsorption kinetics indicated that the adsorption by Co₃O₄–SiPrNH₂/PW₁₂ was well‐modeled using pseudo‐second‐order kinetic model. Finally, thermodynamic parameters revealed that the adsorption was endothermic and spontaneous. The adsorption rate and ability of the Co₃O₄–SiPrNH₂/PW₁₂ were enhanced as compared with Co₃O₄ and Co₃O₄–SiPrNH₂ samples due to enhanced electrostatic attraction intraction. The nanohybride was easily separated and reused without any change in structure. Thus, it could be a promising green adsorbent for removing organic pollutants in water.