Freundlich Isotherm Research Articles

Production of N–Mg doped biochars for phosphate adsorption from renewable sources

It is crucial for the environment, the economy, and society to create low-cost adsorbents from renewable resources to remove phosphate from aqueous effluents. Here, two renewablecarbon and nitrogen sources (Douglas fir and Chitosan) were used to produce engineered N-doped biochars modified with Mg for PO43− adsorption. Mg–N doped biochars were prepared using an impregnation-carbonization process. A central composite experimental design was used to select combinations of independent variables to maximize phosphate adsorption capacity. Phosphate adsorption isotherms were fitted with Langmuir and Freundlich isotherms. The biochar produced at 700 °C, 12 wt % MgCl2, and Douglas Fir/Chitosan ratio: 1/1, which has the highest PO43− adsorption capacity, was further studied. Proximate analysis, elemental composition, surface area, pore size distribution, X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy (FTIR), and Scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (SEM-EDX) were used to characterize this biochar. This biochar has an adsorption capacity of 112.4 mg PO43−/g char. Its phosphate adsorption rate was adjusted to a pseudo-second-order kinetic model. The phosphate adsorption capacity of the biochar produced was comparable with the most effective biochar reported in the literature.

Efficient Removal of Pb(II) Ion Using Tio2/Zno/Sio2 Nanocomposite from Aqueous Solutions Via Adsorption-Photocatalysis Process

This research aims to investigate the usage of a TiO2/ZnO/SiO2 (TZS) composite prepared via a 24-h hydrothermal process at 180° C to remove Pb(II) through adsorption-photocatalysis. Pb(II) exposure has known health risks, making this study significant. The research explores the impact of pH, the nanocomposite quantity, and contact time in the process. Adsorption-photocatalysis was carried out in the dark for 60 min, followed by irradiation with a 160-watt mercury lamp. The adsorption process of Pb(II) ion removal adhered to the pseudo-second-order model regarding kinetics, while the adsorption isotherm corresponded to the Freundlich isotherm. Additionally, the assessment of photocatalysis kinetics showed that the removal of Pb(II) ions followed a pseudo-first-order model, resulting in a 99.58% elimination of Pb(II) ions. Post-adsorption-photocatalytic treatment, a yellowish precipitate was observed. The XRD pattern result of the yellowish precipitate confirmed the presence of PbO as the formed Pb phase. The study concludes that the TiO2/ZnO/SiO2 nanocomposite as adsorbent-photocatalyst is a highly effective, efficient, and promising method to remove Pb(II) contamination from aqueous solutions.

Improving Adsorption Efficiency of Recycled Activated Carbon from Household Water Purifiers through Sonication

Objectives:This study evaluated the potential of recycled activated carbon from household water purifiers as an adsorbent for removing methylene blue. It aimed to achieve resource recycling and dyeing wastewater treatment through the sonication modification of recycled activated carbon.Methods:After sieving recycled activated carbon from water purifiers to a particle size of 75-150μm, the material, in this paper referred to as PCB-S, was processed using sonication to enhance its adsorption capacity. The characteristics of PCB-S were analyzed using SEM, XRD and BET analysis. To evaluate its efficacy, adsorption experiments were carried out varying the following parameters: PCB-S dosage (0.05-0.6gL-1), pH (2.0-10.0), initial concentration of methylene blue (100mgL-1), reaction time (1440 min), and temperature (298 K). The data from these experiments were analyzed using first and second-order kinetic models to understand the reaction kinetics, and the adsorption efficiency was further compared using Langmuir and Freundlich isotherm models. Finally, the thermodynamic properties of the adsorption process between PCB-S and methylene blue were studied to determine its endothermic nature and spontaneity.Results and Discussion:The analysis of the surface characteristics of PCB and PCB-S revealed that sonication significantly altered the pore structure of the activated carbon, leading to increases in both the specific surface area and pore volume. XRD analysis, indicated that sonication had no impact on the crystalline or amorphous structure of the activated carbon. PCB-S demonstrated superior porosity and adsorption capabilities compared to PCB. With a dosage of 0.6gL-1, PCB-S was able to remove 65% of methylene blue from the solution. The adsorption kinetics were best described by a pseudo-second-order kinetic model, with the Langmuir adsorption isotherm fitting the data most accurately. The Gibbs free energy (-1.90~-1.32kJ mol-1) and enthalpy change (7.44 kJ mol-1) confirmed that the adsorption reaction was endothermic.Conclusion:This study confirmed that recycled activated carbon from water purifiers exhibits excellent effectiveness as a dye removal adsorbent when subjected to sonication treatment. Therefore, the possibility of utilizing recycled household water purifier filters as adsorbents is expected to contribute to reducing waste disposal costs by promoting resource recycling.

Synthesis of CS-Fe3O4/GO nanocomposite for adsorption of heavy metal in aqueous environment.

In this study, magnetic material based on graphene oxide (GO) was developed for enhanced adsorption capacity for heavy metals. The Fe3O4 nanoparticles were combined with the GO material using a chitosan (CS) binder to obtain the CS-Fe3O4/GO nanocomposite. The adsorption capacity of this nanocomposite was evaluated by removing heavy metals including Ni2+ ions. When GO was composed with Fe3O4 and CS, the GO films were densely covered with ferromagnetic particles, which were bound and densely distributed on the GO film surface due to the interaction between GO and CS. The optimal conditions for the complexation of Ni2+ and 4-(2-pyridyl azo)-rezoxine (PAR) are 1 mL Ni2+, 2 mL PAR 100 mg/L, pH = 6 (adjusted with 0.7 mL of the 0.1 M K2HPO4 solution) and a complexation time of 20 min. After 50 min of adsorption, the Ni2+ removal efficiency of the CS-Fe3O4/GO nanocomposite reached 81.21 % and the corresponding adsorption capacity was 2.03 mg/g. The Ni2+ removal process followed the first-order model and Freundlich isotherm. This process was spontaneous (∆Go < 0) and an exothermic process (∆Ho = -1128.875 J.mol-1). In addition, the factors affecting this process were investigated, including the pH solution, the dosage of the CS-Fe3O4/GO nanocomposite and the initial Ni2+ concentration. The CS-Fe3O4/GO nanocomposite showed a potential adsorption capacity in removing Ni2+ at low concentrations from wastewater.

Sustainable Napier Grass (Pennisetum purpureum) Biochar for the Sorptive Removal of Acid Orange 7 (AO7) from Water

The unregulated discharge of synthetic dyes from various anthropogenic and industrial activities has resulted in the contamination of different environmental compartments. These dyes can contaminate water bodies, soil, and even the air, resulting in many environmental and health issues. True colors may persist for long periods, thereby affecting the aesthetics and ecology of dye-contaminated areas. Furthermore, they pose potential risks to aquatic life and human health through the ingestion or absorption of dye-contaminated water or food. Acid orange 7 (AO7) is a synthetic azo dye used in the textile, tanning, food, pharmaceutical, paint, electronics, cosmetics, and paper and pulp industries. AO7 can have various human health implications, such as dermatitis, nausea, severe headache, respiratory tract irritation, and bone marrow depletion, due to its high toxicity, mutagenicity, and carcinogenicity. Efforts to regulate and mitigate dye pollution (AO7) are crucial for environmental sustainability and public health. Therefore, this study aimed to remove AO7 from water using sustainable biochar. This objective was accomplished by pyrolyzing dried Napier grass at 700 °C to develop affordable and sustainable Napier grass biochar (NGBC700). The developed biochar was characterized for its surface morphology, surface functional groups, surface area, and elemental composition. The yield, moisture content, and ash content of the NGBC700 were approximately 31%, 6%, and 21%, respectively. The NGBC700’s BET (Brunauer–Emmett–Teller) surface area was 108 . Batch sorption studies were carried out at different pH levels (2–10), biochar dosages (1, 2, 3, and 4 ), and AO7 concentrations (10, 20, and 30 . The kinetic data were better fitted to the pseudo-second-order (PSO) equation (R2 = 0.964–0.997) than the pseudo-first-order (PFO) equation (R2 = 0.789–0.988). The Freundlich isotherm equation (R2 = 0.965–0.994) fitted the sorption equilibrium data better than the Langmuir equation (R2 = 0.788–0.987), suggesting AO7 sorption on heterogenous NGBC700. The maximum monolayer AO7 adsorption capacities of the NGBC700 were 14.3, 12.7, and 8.4 at 10, 25, and 40 °C, respectively. The column AO7 sorption capacity was 4.4. Fixed-bed AO7 sorption data were fitted to the Thomas and Yoon–Nelson column models. The NGBC700 efficiently removed AO7 from locally available dye-laden wastewater. NGBC700 was regenerated using different NaOH concentrations. Possible interactions contributing to AO7 sorption on NGBC700 include hydrogen bonding, electrostatic interactions, and π–π electron donor–acceptor attractions. The estimated total preparation cost of NGBC700 was US$ 6.02 kg−1. The developed sustainable NGBC700 is potentially cost-effective and environmentally friendly, and it utilizes waste (Napier grass) to eliminate fatal AO7 dye from aqueous media.

EDTA functionalized pine needle biochar (EDTA@BC); a valorized bio-material for removal of Ni(II) from aqueous solution.

The preparation of ethylenediaminetetraacetic acid (EDTA) functionalized pine needles biochar (EDTA@BC) as a low-cost active adsorbent and its effectiveness in removing Ni(II) from aqueous solution at various conditions is reported in this paper. First, alkali activation was selected to render the pine needle biochar with an excellent porous structure and increased concentration of hydroxyl groups to facilitate grafting. Subsequently, a simple method was utilized to graft EDTA onto the biochar. The prepared EDTA@BC was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy dispersive x-ray spectrometry (EDX). Batch adsorption studies were conducted to assess the impact of various parameters such as solution pH, adsorbent dosage, adsorbate volume, and shaking time on the removal efficiency of Ni(II). At pH 6, 100 mg dosage, 4 mL of adsorbate volume, and 10 min of shaking time, the maximum removal efficiency of Ni(II) was observed to be 89%. EDTA@BC showed reasonable sorption performance still after the third cycle of regeneration. The effect of interfering ions such as Pb, Cr, Cu, and Hg was evaluated, resulting a decrease of 69%, 78%, 76%, and 68%, respectively, in its sorption capacity. The Langmuir model provided a better fit for Ni(II) in the concentration range of 0.1-2000 ppm under optimized conditions, with qmax of 46.69 ± 1.031 mg/g and KL of 0.001, compared with the Freundlich isotherm, which yielded n = 0.234 and χ2 = 2.7899, Temkin isotherm (R2 = 0.9520), and Redlich-Peterson isotherm (R2 = 0.9725). The removal of Ni(II) by EDTA@BC was found to be the pseudo-second-order kinetics. Thermodynamic studies indicated adsorption process to be endothermic and nonspontaneous. Hence, a sustainable valorized bio-material (EDTA@BC) is prepared having better sorption efficiency of Ni(II) from aqueous solution with possible wide applicability. RESEARCH HIGHLIGHTS: New EDTA functionalized indigenous pine needles biochar (EDTA@BC) was prepared. This low-cost active adsorbent found effective in removing Ni(II) from aqueous solution. FTIR, SEM, and EDX proved synthesis and uptake of Ni(II) from aqueous solution. Ni(II) removal, regeneration, interfering and adsorption studies were performed by UV-Vis spectroscopy.

Modelling and optimising the performance of graphene oxide-Cu2SnS3-polyaniline nanocomposite as an adsorbent for mercury ion removal.

Finding a cost-effective, efficient, and environmentally friendly technique for the removal of mercury ion (Hg2+) in water and wastewater can be a challenging task. This paper presents a novel and efficient adsorbent known as the graphene oxide-Cu2SnS3-polyaniline (GO-CTS-PANI) nanocomposite, which was synthesised and utilised to eliminate Hg2+ from water samples. The soft-soft interaction between Hg2+ and sulphur atoms besides chelating interaction between -N and Hg2+ is the main mechanism for Hg2+ adsorption onto the GO-CTS-PANI adsorbent. Various characterisation techniques, including Fourier transform infrared spectrophotometry (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), elemental mapping analysis, and X-ray diffraction analysis (XRD), were employed to analyse the adsorbent. The Box-Behnken method, utilising Design Expert Version 7.0.0, was employed to optimise the crucial factors influencing the adsorption process, such as pH, adsorbent quantity, and contact time. The results indicated that the most efficient adsorption occurred at pH 6.5, with 12mg of GO-CTS-PANI adsorbent, and 30-min contact time that results in a maximum removal rate of 95% for 50mg/L Hg2+ ions. The study also investigated the isotherm and kinetics of the adsorption process that the adsorption of Hg2+ onto the adsorbent happened in sequential layers (Freundlich isotherm) and followed by the pseudo-second-order kinetic model. Furthermore, response surface methodology (RSM) analysis indicates that pH is the most influential parameter in enhancing adsorption efficiency. In addition to traditional models, this study employed some artificial intelligence (AI) methods including the Random Forest algorithm to enhance the prediction of adsorption process efficiency. The findings demonstrated that the Random Forest algorithm exhibited high accuracy with a correlation coefficient of 0.98 between actual and predicted adsorption rates. This study highlights the potential of the GO-CTS-PANI nanocomposite for effectively removing of Hg2+ ions from water resources.

Optimization of batch process parameters for chromium (VI) removal from synthetic wastewater using eggshell–clay composite

In this study, a biodegradable spherical adsorbent bead was developed from eggshell (ES) and Bijoypur clay (BC) for the removal of hexavalent chromium from synthetic tannery wastewater. This Eggshell–Clay polymer composite (ES–BC) was made by incorporating them with PVA and alginate. To analyze the morphology and chemical composition of the adsorbent before and after the chromium adsorption, SEM, FTIR, XRD, and EDX were used. The impact of adsorption parameters such as adsorbent dosage (0.67–2.23 g/L), pH of the solution (1.5–9), contact time (10–240 min), initial Cr (VI) concentration (25–100 ppm), and solution temperature (25–65 °C), percentage clay in ES-BC adsorbent (0–40%) for Cr (VI) adsorption were investigated. The optimum value for adsorbent dosage, pH, contact time, initial Cr concentration, temperature, and clay to eggshell ratio was found 1.17 g/L, 1.5, 150 min, 58.2 ppm, 25 °C, and 80/20% respectively. The isotherm model was well-fitted to the Freundlich isotherm suggesting heterogeneous adsorption in multilayer on surface. The adsorption kinetics followed pseudo-second-order kinetics supporting the chemisorption process. Moreover, a decrease in enthalpy (H°) and negative Gibbs free energy (G°) with increased temperature indicated exothermic and spontaneous reaction. Therefore, this research investigated that the composite may serve as a viable option for treating Cr (VI) containing tannery effluent.

Graphene oxide dots‐loaded chitin flask: A sustainable adsorbent for separating multiple dyes from water

AbstractThis research endeavors to comprehensively explore the sorption dynamics of dyes from aqueous solutions utilizing a graphene oxide‐chitin (GO‐chitin) biosorbent. The investigation systematically evaluates the influence of key parameters, including temperature, pH, duration of contact, and initial dye doses, on the sorption efficiency of the biosorbent. Results obtained indicated that at acidic pH range, the dye removal efficacy was more than 80% for methyl orange and Remazol Brilliant Blue. Maximum removal efficacy was achieved within the 30 min of adsorption studies. Notably, the study underscores the remarkable adsorption capacity of GO‐chitin, varies in the range of 75% and 95%, for all three dyes, positioning it as a highly promising material for the remediation of polluted aquatic environments. The adsorption follows pseudo‐second‐order kinetics and Freundlich isotherm. These findings contribute valuable insights into the potential application of GO‐chitin as an effective biosorbent in the context of wastewater treatment, emphasizing its role in addressing environmental challenges associated with dye contamination in aqueous systems.

New Sorption Isotherms Derived from a Gamma Distribution of Binding Constants.

New sorption isotherms for heterogeneous sorbents are derived by combining a Gamma distribution of binding constants with a local isotherm defined by a Langmuir or Hill equation. The new "Gamma isotherms" are expressed as Stieltjes transforms of the distribution and involve generalized exponential integrals. The related energy distributions are asymmetric and present a peak corresponding to the mean binding constant. The advantages of the new isotherms are (1) at low pressures or concentrations, with a Langmuir local isotherm, the global "Gamma-Langmuir" isotherm retrieves Henry's law; (2) contrary to the power Freundlich or hypergeometric Freundlich global isotherms, these Gamma isotherms do not need a redefinition of the standard state; (3) with a Hill local isotherm, the global "Gamma-Hill" isotherm allows a separate estimation of the cooperativity and heterogeneity parameters; and (4) the condensation approximation is a good approximation if the local isotherm is Hill and displays a high degree of cooperativity. The Gamma-Langmuir model is applied to three examples from the literature, with rather different Gamma distributions.

Adsorption of Pb, Cu, and Ni Ions on Activated Carbon Prepared from Oak Cupules: Kinetics and Thermodynamics Studies

Agricultural residue-activated carbon and biochar, inexpensive and environmentally friendly adsorbent materials, have recently received significant research attention. This study investigated the potential use of oak cupules in activated carbon form to remove widespread heavy metals (Pb2+, Cu2+, and Ni2+) from wastewater. The oak-activated carbon was prepared from oak cupules and activated with phosphoric acid. Oak-activated carbon was characterized using FTIR, BET analysis, energy-dispersive X-ray spectrometry (EDS), thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The Freundlich, Langmuir, and Temkin isotherm models were used to assess the equilibrium data. The impact of various parameters, including pH effect, temperature, adsorbent dose, and contact time, was estimated. The Freundlich model was the most agreeable with Pb2+ adsorption by oak-based activated carbon, and Langmuir was more compatible with Cu+2 and Ni+2. Under optimum conditions, the average maximum removal was 63% Pb2+, 60% Cu2+, and 54% Ni2+ when every ion was alone in the aqueous solution. The removal was enhanced to 98% Pb2+, 72% Cu2+, and 60% Ni2+ when found as a mixture. The thermodynamic model revealed that the adsorption of ions by oak-based activated carbon is endothermic. The pseudo-second-order kinetic best describes the adsorption mechanism in this study; it verifies chemical sorption as the rate-limiting step in adsorption mechanisms. The oak-activated carbon was effective in removing Pb2+, Cu2+, and Ni2+ from wastewater and aqueous solutions.

Synthesis of novel bentonite/pectin-grafted-poly(crotonic acid-co-acrylic acid) hydrogel nanocomposite for adsorptive removal of safranin O dye from aqueous solution

ABSTRACT This novel work is devoted to the synthesis of the bentonite/pectin-grafted-poly(crotonic acid-co-acrylic acid (AA-co-CA) hydrogel nanocomposite by free-radical copolymerisation method for exploring its potential towards safranin O dye removal. The prepared nanocomposite was characterised by different techniques revealing the presence of numerous functionalities, porous nature and greater swelling % at basic pH. The pHpzc of the nanocomposite was determined to be 4. Maximum of 97.09% of safranin O dye removal take place under optimised conditions, that is, 0.03 g of bentonite dose (bentonite to net hydrogel weight ratio (1.295%), with pH of 7, nanocomposite dose of 5 g/l for 120 min. The dye concentration was 500 mg/l at the temperature of 25°C. Effect of ionic strength confirmed the greatest decrease in adsorption capacity in the presence of divalent cations. The highest R2 and the lowest error margins of the Freundlich isotherm and pseudo-second-order kinetic models make these models well fitted to the experimental data. Further, the spontaneous and exothermic nature of the process was confirmed by the negative values of ΔG and ΔH, respectively. The enhanced adsorption of safranin O dye by the prepared nanocomposite was informed by several mechanisms, including electrostatic, pore filling and H-bonding. A comparison of the adsorption capacity of the prepared nanocomposite with various other adsorbents was also studied. Stability of the prepared adsorbent was revealed from its recovery upto five cycles in different desorption media. Finally, the treatment of the adsorbent with real textile wastewater showed its removal efficiency as 95.8% highlighting its promising nature for treating large industrial wastewater.

Photocatalytic degradation of Direct Black 10 B dye in aqueous phase using nanophotocatalyst

ABSTRACT In this study, the photocatalytic degradation of an aqueous solution containing a mixture of Direct Black 10 B dye using titanium dioxide (TiO2) as a catalyst was investigated. The degradation of Direct Black 10 B dye was studied for several parameters, including the catalyst, dosage, initial concentration of dye, and pH. Variable catalyst quantities (0.25, 0.50, 0.75, 1, and 1.25 g), pH (3, 5, 9, and 11), and beginning dye concentration were used in the studies (62.5, 125, 250 and 500 ppm). 0.75 g/litre of catalyst was found to be the ideal dose. The ideal catalyst concentration was determined to be 0.75 g/litre, and the maximal dye decolourization rate was further studied in a basic media, i.e. at pH 9 Blue turned into grey and finally white in the acidic medium, whereas blue turned into pink and then white in the basic medium. After 3 hours 98% of the colour was completely removed at this optimal point. The Langmuir, Freundlich and Temkin isotherms were examined. The langmuier isothers with regression coefficient 0.99 is best fitted as compared to Freundlich and Temkin isotherms. The findings of the kinetic analysis suggest that the Pseudo Second order with regression coefficient 0.9923 is best suited as compared with the pseudo first order and Intra-particle diffusion model.

Equilibrium, Kinetic, and Diffusion Mechanism of lead(II) and cadmium(II) Adsorption onto Commercial Activated Carbons

The adsorption of Pb(II) and Cd(II) on three commercial microporous activated carbons was analysed. Adsorption kinetics and statistics were investigated, and the results were described with different models. The highest values of the correlation coefficient R2 were obtained for the pseudo-second-order kinetics model for all ions tested and all sorbents used. The adsorption process was found to be determined by both diffusion in the liquid layer and intraparticle diffusion. The adsorption equilibrium is very well described by Langmuir, Temkin, Thoth or Jovanovic isotherm models. Based on the values of n from the Freundlich isotherm and KL from the Langmuir isotherm, the adsorption of cadmium and lead ions was found to be favourable. The highest monolayer capacities were obtained during the adsorption of lead ions (162.19 mg/g) and for cadmium (126.34 mg/g) for activated carbon WG-12. This carbon is characterised by the highest amount of acid functional groups and the largest specific surface area. The adsorption efficiency of the tested ions from natural water is lower than that from a model solution made from deionised water. The lowest efficiencies are obtained when the process occurs from highly mineralised water.

Preparation and Application of Responsive Nanocellulose Composites

Cellulose nanofibrils/poly(N-Isopropylacrylamide) semi-interpenetrating networks (MMCNF-PNAs) were synthesized using an in situ fabrication (semi-IPN). The polymerization of N-isopropylacrylamide (NIPAM) (free radical) was conducted in the presence of magnetic modified cellulose nanofibrils (MMCNFs). The adsorption behaviors and surface morphology of the synthesized adsorbents were investigated systematically. The adsorption behaviors of the as-prepared MMCNF-PNA towards methylene blue (MB, as the model contaminant) dye was studied, and the optimal adsorption conditions were also studied. The adsorption processes could be well fitted using pseudo-second-order and Elovich kinetic models. Meanwhile, Langmuir and Freundlich isotherm models were used to fit the adsorption which occurred at 25, 37 and 65 °C. The corresponding results showed that the Freundlich isotherm model fitted the adsorption process better, indicating that the dye’s adsorption happened via heterogeneous adsorptive energies on the prepared MMCNF-PNAs. Their desorption and reusability were also studied to verify magnetic responsivity. To sum up, MMCNF-PNAs are promising magnetic and thermal stimuli-responsive adsorbents, showing a controlled adsorption/desorption process.

Fluoride removal by hydroxyapatite modified with anhydrous aluminum chloride

ABSTRACT Efficient and low-cost removal of fluoride from water has attracted wide attention. Here, aluminum-modified hydroxyapatite (Al-HAP) was prepared by a homogeneous hydrothermal co-precipitation method. The physicochemical properties of the Al-HAP surface were characterized by SEM, XRD, FT-IR, BET, and zeta potential, and the adsorption performances were evaluated. It showed that Al-HAP has a larger specific surface area (121.97 m2/g, which is 2.3 times larger than that of HAP), more surface-active hydroxyls and positively charged at pH less than 7, which indicate that Al-HAP is beneficial to the adsorption of negatively charged fluoride. Al-HAP had a higher fluoride adsorption capacity (56.44 mg/g) than that of HAP (28.36 mg/g), and not sensitive to the interference of coexisting ions except CO32-. Based on the adsorption kinetics and adsorption isotherm experiments, the proposed two-stage kinetic model and Freundlich isotherm model can better describe the adsorption process. From the results of XPS and FT-IR, it indicated that the ion exchange between hydroxyl group on the surface and fluoride ions is the main driven force for the adsorption, and electrostatic adsorption is also helpful. The present study provides an improved HAP to effectively remove fluoride from water.

Graphene oxide intercalated Alk-MXene adsorbents for efficient removal of Malachite green and Congo red from aqueous solutions

Currently, adsorbents with high adsorption performance for eliminating pollutants from discharged wastewater have received many researchers’ attention. To this aim, a novel AMXGO absorbent was fabricated by intercalating graphene oxide (GO) into alkalized MXene (Alk-MXene) layer which exhibited high efficacy for the removal of cationic Malachite Green (MG) and anionic Congo Red (CR). Analysis of FTIR, XRD, SEM and TG presented that AMXGO absorbent have a typical three-dimensional layer by layer structure and abundant oxygen-containing groups and its thermal stability was remarkably improved. BET results elucidated that AMXGO1 adsorbent has larger specific surface area and pore volume (16.686 m2 g−1, 0.04733 cm3 g−1) as compared to Alk-MXene (4.729 m2 g−1, 0.02522 cm3 g−1). A dependence of adsorption performance on mass ratio between Alk-MXene and GO, initial dye concentration, contact time, temperature and pH was revealed. Maximum adsorption capacity of MG (1111.6 mg/g) and CR (1133.7 mg/g) were particularly found for AMXGO1 absorbent with a mass ratio of 3:1 and its removal for both dyes were higher than 92%. The adsorption process of AMXGO1 adsorbent for both MG and CR complies with pseudo-second-order kinetic model and Freundlich isotherm model. In addition, adsorption mechanism was explored that synergism effects as electrostatic attraction, π-π conjugates, intercalation adsorption and pore filling were the main driving force for the high adsorption performance of dye. Therefore, AMXGO adsorbent has a potential application prospect in the purification of dye wastewater.

An N-Rich Polymer for the Selective Recovery of Gold from Wastewater.

The recovery of valuable gold from wastewater is of great interest because of the widespread use of the precious metal in various fields and the pollution generated by gold-containing wastes in water. In this paper, a water-insoluble cross-linked adsorbent material (TE) based on cyanuric chloride (TCT) and ethylenediamine (EDA) was designed and used for the adsorption of Au(III) from wastewater. It was found that TE showed extremely high selectivity (D = 49,213.46) and adsorption capacity (256.19 mg/g) for Au(III) under acidic conditions. The adsorption rate remained above 90% eVen after five adsorption-desorption cycles. The adsorption process followed the pseudo-first-order kinetic model and the Freundlich isotherm model, suggesting that physical adsorption with a multilayer molecular overlay dominates. Meanwhile, the adsorption mechanism was obtained by DFT calculation and XPS analysis, and the adsorption mechanism was mainly the electrostatic interaction and electron transfer between the protonated N atoms in the adsorbent (TE) and AuCl4-, which resulted in the redox reaction. The whole adsorption process was the result of the simultaneous action of physical and chemical adsorption. In conclusion, the adsorbent material TE shows great potential for gold adsorption and recovery.

Sustainable Banana-Waste-Derived Biosorbent for Congo Red Removal from Aqueous Solutions: Kinetics, Equilibrium, and Breakthrough Studies

This study investigates the adsorption of Congo red (CR) dye from wastewater using banana peel biochar (BPBC) in both batch and fixed-bed column modes. BPBC was characterized using FTIR, SEM, XRD, TGA, and BET analysis, revealing a predominantly mesoporous structure with a surface area of 9.65 m2/g. Batch adsorption experiments evaluated the effectiveness of BPBC in removing CR, investigating the influence of the BPBC dosage, initial CR concentration, and solution pH. Results showed optimal CR removal at pH levels below 4, suggesting a favorable electrostatic interaction between the adsorbent and the dye. Furthermore, a pseudo-first-order kinetic model best described the adsorption process. The Freundlich isotherm provided a better fit compared to the Langmuir and Dubinin–Radushkevich (D-R) models, implying a heterogeneous adsorption surface. The calculated maximum adsorption capacity (Qm) from the Langmuir model was 35.46 mg/g. To assess continuous operation, breakthrough curves were obtained in fixed-bed column experiments with varying bed heights (1–3.6 cm). The results demonstrated efficient CR removal by BPBC, highlighting its potential for wastewater treatment. Finally, this study explored the feasibility of BPBC regeneration and reuse through four adsorption–desorption cycles.

Application of Cotton Stalk as an Adsorbent for Copper(II) Ions in Sustainable Wastewater Treatment

The capacity of untreated cotton stalk to remove and adsorb Cu2+ ions in synthetic and natural aqueous solutions was evaluated. The influence of three sensitive parameters of the adsorption process—solution pH, adsorbent dosage, and contact time—on the percentage of Cu2+ removal in agricultural wastewater, livestock wastewater, and synthetic samples was studied. Physicochemical and morphological properties were studied using thermogravimetry, Fourier infrared spectrophotometry, and scanning electron microscopy. The elemental composition, proximal composition, zero charge point, and acid–base sites were determined. In addition, kinetic studies were performed, and the adsorption equilibrium was analyzed. The optimum conditions for Cu2+ adsorption were the following: solution pH = 5.5, adsorbent dosage of 0.6 g, and contact time of 60 min. Under these conditions, the percentage of Cu2+ removal in synthetic samples was 66.5% when the initial copper concentration was 50 mg/L. The removal percentage in agricultural and livestock wastewater samples was 87.60% and 85.05%, respectively, when the initial copper concentration was 25 mg/L. The adsorption data are consistent with the Freundlich isotherm model, which achieved a quadratic fit of 0.991 compared to 0.5542 for the Langmuir model. The experimental results indicate that the adsorption adequately fits the pseudo-second-order kinetic model. The results suggest that cotton stalks are a promising adsorbent for the ecological and economical removal of Cu2+ in wastewater. This research, therefore, provides relevant information that contributes to the sustainable management of agricultural waste and instills hope for a reduction in water pollution from heavy metals derived from agricultural activities.