Batch Adsorption Research Articles

Hydrothermal chemical modification of red mud for efficient adsorption of methylene blue

ABSTRACT Red mud (RM) is the industrial solid waste produced after alumina extraction from bauxite, and most RM is directly discharged to the landfill yards without any treatment. In this study, modified red mud (MRM) was synthesized by a hydrothermal chemical modification method as an efficient adsorbent for methylene blue (MB) removal. The prepared MRM was characterized by X-ray fluorescence spectroscopy, X-ray diffraction, scanning electron microscope, transmission electron microscope, and Fourier transform infrared spectrometer. The effects of reaction time, initial MB concentrations, MRM dosage, temperature, and system pH were investigated in the MB batch adsorption experiments. The results showed that the modification method increased the specific surface area of RM material from 16.72 to 414.47 m2/g. The maximum adsorption capacity of MRM for MB was 280.18 mg/g under the conditions of initial MB concentration of 1000 mg/L, reaction time of 300 min, temperature of 25 ℃, and natural pH of 6.06. Meanwhile, the adsorption kinetics and equilibrium isotherms were demonstrated to fit well with the pseudo-second-order kinetic model and Temkin isotherm, respectively. This study provides a new method for the valorization of RM and demonstrates that MRM can be used as a low cost and environmentally friendly potential adsorbent for the removal of MB from wastewater.

Cellulose/castor oil‐based polyurethane film composite for aqueous Cd and Pb adsorption: Evaluation using laser‐induced breakdown spectroscopy

AbstractCastor oil‐based polyurethane has been researched for its utility in heavy metal adsorption. To improve the adsorptive performance, the polymer can be incorporated with cellulose—a renewable and widely available biopolymer. The aim of this research was to synthesize a film composite prepared from castor oil‐based polyurethane and cellulose for adsorptive removal of aqueous Cd and Pb. One‐shoot synthesis method was employed by mixing cellulose filler with castor oil and toluene diisocyanate (TDI). Characterization was carried out by FT‐IR, SEM, TGA, DSC, and contact angle analyses. Batch adsorption was carried out for the Cd and Pb with variations in contact time and initial pH, before analyzed for the adsorptive performance using 1064 nm Nd:YAG laser spectroscopy. The resulted adsorbents had improved thermal stability, and lower hydrophobicity. Adsorption of Pb and Cd increased 2 and 35 times after the addition of 0.1 g cellulose, respectively. Batch adsorption test revealed that the optimum conditions are 120‐min contact time and pH of 9 and 7 (for Cd and Pb, respectively). In conclusion, incorporation of cellulose could modify the characteristics of castor oil‐based polyurethane film and improve the adsorption of Cd and Pb.

Sustainable heavy metal (Cr(VI) ion) remediation: Ternary blend approach with chitosan, carboxymethyl cellulose, and bioactive glass

Heavy metal pollution poses a significant environmental challenge to worldwide, especially in developing countries. This study focuses on eliminating the heavy metal chromium (VI) ion from wastewater, employing an eco-friendly and economical ternary blend composed of Chitosan (CS), Carboxymethyl cellulose (CMC), and bioactive glass (BAG). The innovative bioactive glass is crafted from biosilica extracted from biowaste of cow dung ash, calcium oxide from eggshell ash, and phosphorus pentoxide. The CS/CMC/BAG blend is prepared via sol-gel method and characterized using XRD, FT-IR, TGA, BET, TEM and SEM revealing a porous structural morphology during blending. Batch adsorption studies explore various parameters such as pH, adsorbent dose, contact time and initial metal ion concentrations. The results are then evaluated through adsorption kinetics and adsorption isotherms (Langmuir, Freundlich, D-R, and Temkin isotherm modeling). The investigation concludes that the optimal conditions for Cr (VI) removal are pH 3, contact time of 300 min, adsorbent dosage of 0.5 g, and an initial metal ion concentration of 50 ppm. The adsorption isotherm model indicates an excellent fit with the Freundlich isotherm (R2 = 0.9576) and pseudo-second-order kinetics (R2 = 0.981). In summary, the CS/CMC/BAG ternary blend exhibits a remarkable ability to effectively remove heavy metal Cr(VI) ions from industrial wastewater.

Simultaneous removal of lead(II) and cadmium(II) from acidic wastewater by Fe-modified sludge biochar

In natural environments, heavy metal water pollution often involves simultaneous presence of various heavy metal ions (HMs), posing significant challenges for their removal. In this study, Fe-modified sludge biochar was synthesized via the co-precipitation method, and the effects of various environmental factors on simultaneously removing lead(II) and cadmium(II) by Fe@SBC were investigated. Batch adsorption experiments showed that Fe@SBC has a higher removal capacities for Pb(II) than for Cd(II) in both single or binary solutions. Increasing solution pH promoted the HMs removal on Fe@SBC. Coexisting divalent cations (Mg2+ and Ca2+) exhibited stronger inhibitory effects on HMs removal by Fe@SBC than monovalent cations (K+ and Na+). The presence of humic acid (HA) did not affect Pb(II) removal on Fe@SBC in either single or binary systems. In single systems, increasing HA concentration enhanced Cd(II) removing on Fe@SBC, while in binary systems, increasing HA concentrations inhibited the Cd(II) removal on Fe@SBC. The sorption of Pb(II) and Cd(II) on Fe@SBC followed the pseudo-second-order kinetic model and the Langmuir model. The removal mechanisms involved electrostatic interactions, complexation with O-containing group, and mineral dissolution-precipitation. After three regenerations, the adsorption capacity of Fe@SBC for Pb(II) and Cd(II) decreased by approximately 5–10 %. In summary, this environmentally friendly composite material has great potential for simultaneously remediating of Pb(II) and Cd(II).

Facile green fabrication of MIL‐101(Cr)/PVA nanofiber composite as effective, stable, and reusable adsorbent for cationic dye removal

AbstractIn this study, chromium‐based metal–organic framework (MIL‐101(Cr)) was incorporated into polyvinyl alcohol nanofibers (PVA NFs) via green electrospinning followed by heat treatment to fabricate MIL‐101(Cr)@PVA NFs composite without the need for any organic solvent or other dispersants. The fabricated MIL‐101(Cr)@PVA NFs were comprehensively characterized using a suite of common techniques. Morphological characteristics of MIL‐101(Cr)@PVA NFs showed a fibrous structure with an average diameter of 228 ± 37 nm and decorated with MIL‐101(Cr) particles arranged in a nanoneedle‐like pattern. Subsequently, its adsorption efficiency towards the cationic crystal violet dye (CV) was evaluated through batch adsorption experiments. The influence of various experimental parameters on CV removal efficiency was systematically optimized using a factorial design approach. The Langmuir isotherm and kinetic pseudo‐second‐order (PSO) model provided an excellent fit to the adsorption equilibrium data, indicating a maximum adsorption capacity (qmax) of 344.18 mg/g for MIL‐101(Cr)@PVA NFs compared with 83.94 mg/g for pristine PVA NFs. Furthermore, the MIL‐101(Cr)@PVA NFs composite demonstrated excellent reusability and stability, maintaining a significant portion of its removal capacity even after six adsorption–desorption cycles. These findings highlight the potential of the fabricated composite as a highly efficient and reusable adsorbent for CV removal from wastewater treatment applications.Highlights The MIL‐101(Cr)@PVA NFs nanocomposite fabricated by electrospinning technique. The MIL‐101(Cr) particle arranged in a nanoneedle‐like pattern in the PVA NFs. Incorporation of MIL‐101(Cr) improved qmax of PVA by 391.5%. The MIL‐101(Cr)@PVA NFs membrane has excellent stability and reusability.

Insights on the Contradiction between the Affinity and Capacity of Ferrihydrite toward As(III) and As(V): Surface Reaction Revisited.

Ferrihydrite is omnipresent in nature, and its adsorption of As(III/V) decides the migration of arsenic. Although As(III) is commonly recognized as the more mobile species of inorganic arsenic, it sometimes exhibits less mobility in ferrihydrite systems, which calls for further insights. In this study, we elucidated the adsorption behavior and mechanisms of As(III/V) on ferrihydrite under different loading levels (molar ratio As/Fe = 0-0.38), solution pH (3-10), and coexisting ions [P(V) and Ca(II)] based on batch adsorption experiments, surface complexation modeling, density functional theory calculations, and X-ray photoelectron spectroscopy. Our results show that As(III) exhibits weaker adsorption affinity but a larger capacity compared with that of As(V). On ferrihydrite, As(III) and As(V) are adsorbed mainly as bidentate mononuclear complexes at type-a sites [≡Fe(OH-0.5)2] and bidentate binuclear complexes at type-b sites (2≡FeOH-0.5), respectively. As the dosage increases, As(III) further forms mononuclear monodentate complexes at both surface sites, resulting in a higher site utilization efficiency, while As(V) does not due to repulsive electrostatic interaction. The difference in surface species of As(III/V) also leads to complex responses when coexisting with high concentrations of P(V) and Ca(II). This study helps us to understand environmental behavior of As(III/V) and develop remediation strategy in As(III/V) contaminated systems.

PSf Membrane-Impregnated Jute-Copper Nanocomposite as Highly Efficient Dye Removal Material.

Water pollution, driven by the discharge of dyes from industrial processes, poses a significant environmental and health hazard worldwide. Methylene blue, a common dye, constitutes particular concern due to its persistence and toxicity. Conventional wastewater treatment methods often struggle to effectively remove such contaminants. In this study, we introduce a novel approach utilizing a polysulfone-based composite membrane incorporating pretreated jute fibers and copper nanoparticles for the removal of methylene blue from aqueous solutions. The pretreated jute fibers undergo alkali and hydrogen peroxide treatments to enhance their adsorption capabilities, while copper nanoparticles are incorporated into the membrane to bolster its antimicrobial properties. Through comprehensive characterization techniques, including Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS), and scanning electron microscopy (SEM), we confirm the structural and chemical properties of the composite membranes. Batch adsorption studies reveal the superior performance of the composite membrane compared with individual components. Specifically, at lower methylene blue concentrations (∼20 ppm), the composite membrane demonstrates a remarkable percent removal value of about 97%, while at higher concentrations (∼100 ppm), the percent removal remains substantial at 85%. Additionally, desorption studies elucidate the retention capacity of the adsorbed dye, indicating the feasibility of the composite membrane for practical applications in wastewater treatment. These findings underscore the potential of nanocomposite-fiber membranes as sustainable and cost-effective solutions for mitigating water pollution. By harnessing advancements in nanotechnology and materials science, the presented innovative composite membranes could offer promising avenues for addressing water pollution challenges and promoting environmental sustainability.

Removal of Ammonia and Colour from Landfill Leachate using Integrated Electrocoagulation-Zeolite Adsorption Processes

The amount of waste generated in Malaysia had increased annually due to both economic and population accelerations. This resulted in an increase in leachate production that contains a high amount of ammonia nitrogen (NH3-N) and colour, which is a severe problem for both environments as well as for human health. Therefore, this study aimed to determine the potential of Electrocoagulation (EC) – zeolite adsorption for removing NH3-N and colour from landfill leachate. In the experimental works, two batch studies consist of batch EC using aluminium (Al) cylindrical electrode and batch adsorption study using clinoptilolite zeolites adsorbent were conducted using leachate sample collected from Pulau Burung Sanitary Landfill (PBSL). The batch EC experiment was carried out to determine the optimum removal of NH3-N and colour by the effect of current density (7 - 35 mA/mm2), initial pH (5 - 9), electrolysis time (0 - 90 minutes) and inter-electrode distance (5 - 25 mm). An integrated EC - zeolite adsorption was carried out under the optimum condition of 2.0 g/150 mL adsorbent dosage, contact time of 100 minutes and an initial pH value of 8. Based on the experiment, almost 50% of NH3-N and 95% of colour were removed using a single EC under the optimum current density of 14.0 mA/mm2, pH 5, electrolysis time of 75 minutes and 15 mm of inter-electrode distance. A comparison of colour removal between single EC and EC-Zeolite showed the same degradation performance. The interaction of hydrogen ion (H+) with aluminium hydroxide ion (Al (OH)3) produces during EC stabilises small particles forming larger sludge that reduces colour concentration. The removal of NH3-N increased from 50.0% to 93% when EC was integrated with clinoptilolite zeolite adsorption. In conclusion, the results show that both processes can potentially remove colour while the integrated process effectively removes NH3-N from landfill leachate. The proposed treatment helps optimise process performance while minimising the operational cost of the treatment. Thus, the proposed integrated EC – zeolite adsorption processes can be an alternative to landfill leachate treatment which aligns with the 12thMalaysia Plan to reduce pollution and carbon emissions to become a carbon neutral nation as early as 2050.

Evaluation and optimization of six adsorbents for removal of tetracycline from swine wastewater: Experiments and response surface analysis

The removal of tetracycline antibiotics using adsorbents is becoming an environmentally friendly and cost-effective method. This study systematically analyzed the stability, structure, morphology, and chemical properties of various adsorbents. Batch adsorption experiments (pH, time, temperature, tetracycline concentration, and adsorbent dosage) were conducted to compare the adsorption capacity of the six adsorbents (biochar, activated carbon, montmorillonite, zeolite, chitosan, and polymerized aluminum chloride) for tetracycline removal. The results indicated that montmorillonite had the highest adsorption efficiency, followed by biochar, with chitosan showing the lowest efficiency. At an adsorbent dose of 25 g/L and an initial tetracycline concentration of 120 mg/L, the removal rates of tetracycline by montmorillonite, biochar, and chitosan were 97.6%, 69.3%, and 12.2%, respectively. Furthermore, the removal rate of tetracycline by biochar, following the response surface methodology optimal mode, increased by 5.5%. The Elovich model was better suited to explain the adsorption process of tetracycline compared to the conventional pseudo-first kinetic model and second-order kinetic model. The isothermal adsorption model suggested that both chemisorption and physisorption occurred in all removal processes, in which chemisorption dominated. Tetracycline was efficiently adsorbed through the combined effects of pore filling, electrostatic attraction, π-π interactions, and complexation reactions of surface functional groups. Additionally, montmorillonite demonstrated superior performance as an adsorbent for tetracycline removal from swine wastewater compared to the other adsorbents studied.

Optimization and prediction of dye adsorption utilising cross-linked chitosan-activated charcoal: Response Surface Methodology and machine learning

Water pollution poses a significant environmental threat due to the discharge of organic dyes from industrial processes. In this study, we investigated a novel adsorptive composite material for removing MB dye from water and applied new models for optimizing and predicting adsorption efficiency. The cross-linked chitosan-activated charcoal composite material was synthesized using a single-step process and characterized by analytical techniques including FTIR, XPS, BET, SEM, TGA, and zeta potential, which demonstrated its remarkable physicochemical properties. Batch adsorption experiments showed a direct correlation between increased adsorbent dosage and enhanced MB dye adsorption, with an optimal dosage of 0.4 g/25 mL. Additionally, pH-dependent studies revealed excellent performance at lower pH levels, achieving up to 95 % adsorption. The composite reached equilibrium within the first 360 min of contact time and maintained a stable 99 % adsorption efficiency afterward. These results were confirmed by an applied optimization RSM model. Additionally, adsorption isotherms and kinetics were thoroughly analyzed by fitting them into various models, revealing a maximum dye adsorption capacity of 625 mg/g. ML models, such as RF, XGBoost and stacking, were used to predict adsorption efficiency, with a stacked model combining RF and XGBoost showing the highest predictive accuracy. Variable importance plots indicated that contact time was the most significant factor influencing adsorption, followed by dosage and pH, in line with RSM findings. This research highlights the eco-friendliness and cost-effectiveness of the composite material in addressing water pollution challenges. Integrating ML models and RSM enhances the predictability and optimization of the adsorption process, offering valuable insights for mitigating the impact of organic dyes on aquatic ecosystems and public health.

Synthesis of amidoxime adsorbent prepared by radiation grafting on upcycled low-density polyethylene sheet for removal of heavy metals from wastewater

The issue of discharging waste, especially heavy metals from industrial activities into the environment, not only adversely impacts environmental quality but also has impacts on communities and human health. Removal and reduction of heavy metal contamination in rivers and wastewater are, therefore, critical initiatives that require significant attention. This work studied the removal of heavy metals, including Zn(II), Cu(II), As(III), and Pb(II) by utilizing an upcycled amidoxime low-density polyethylene sheet (AO-sheet). The synthesized AO-sheet was analyzed for various physical properties, including scanning electron microscope, energy-dispersive x-ray spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. For the batch adsorption experiment, parameters affecting adsorption capacity were studied: initial concentration, submerging time, and pH. Adsorption isotherms were also studied. The results of the heavy metal adsorption study showed that the initial concentration was the most significant parameter; the higher the initial concentration, the greater the adsorption capacity. The adsorption capacity of Zn(II) and Pb(II) increased with submersion time, which achieved 21.07 and 0.855 mg/g-adsorbent, respectively, after four weeks of submersion under the highest initial concentration studied. The adsorption capacity of Cu(II) was 7.98 mg/g-adsorbent after two weeks of optimal adsorption duration under the highest initial concentration studied. The adsorption capacity of As(II) was 1.07 mg/g-adsorbent after one week of optimal submersion time under the highest initial concentration studied. Moreover, the appropriate pH range for effective adsorption of Zn(II), Cu(II), and Pb(II) was identified as 8–9, while for As(III), it was 6–8, with an adsorption duration of 0.43 weeks (3 days). From the Langmuir isotherm, it was found that the adsorption of this work was characterized by monolayer adsorption. The results demonstrate that the AO-sheet can be effectively used to remove heavy metals from wastewater. Its potential for reusability was up to 8 cycles, with the Zn(II) adsorption capacity being reduced to about 20.37%.

Application of zirconium aspartic acid metal-organic framework (MIP-202(Zr)) for high efficient ruthenium adsorption from aqueous solutions

The zirconium metal – organic framework MIP-202(Zr), based on L-aspartic acid, was prepared by hydrothermal method and used for study of ruthenium adsorption from aqueous solutions. The obtained material was characterized by X-ray diffraction (XRD), infra red spectroscopy (IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The batch adsorption experiment was performed for determination of adsorption equilibrium, kinetics and thermodynamics parameters to Ru(III) from aqueous solution on MIP-202(Zr). The data of ruthenium sorption onto MIP-202(Zr) were fitted and analyzed by the Langmuir, Freundlich and Temkin equilibrium isotherm models, while the Langumir adsorption isotherm models fit the best. Kinetic data were analyzed by four kinetic models, and ruthenium sorption on MIP202(Zr) can be describes the best by intra particle diffusion (Weber Morris). Analysis of thermodynamic properties of ruthenium ions sorption onto MIP-202(Zr) shows that the sorption process has a spontaneous and endothermic nature and is energetically beneficial.

A green solution for eliminating methylene blue and crystal violet dyes using eco-friendly zinc oxide nanoparticles synthesized from Dracaena trifasciata

Modern technological development has unavoidably resulted in more pollution, especially in aquatic environments. While extensively utilized in various industries, cationic dyes pose a significant threat to both the environment and human health, ranking among the most hazardous pollutants. When exposed to these dyes, one may experience skin irritation and allergic dermatitis because they are frequently mutagenic, toxic, carcinogenic, and resistant to biodegradation. The continued release of these dyes into the environment exacerbates human health and ecosystem concerns. This work investigates the possibility of eco-friendly zinc oxide nanoparticles, which are produced by the co-precipitation method from leaf extracts of the Dracaena trifasciata plant, also referred to as snake plant, for the elimination of the cationic dyes methylene blue and crystal violet. This work presents a novel approach for synthesizing eco-friendly zinc oxide nanoparticles using leaf extract from Dracaena trifasciata. To examine the eco-friendly zinc oxide nanoparticles, characterization studies were carried out using various instrumental methods. The best conditions for removing methylene blue and crystal violet were found through batch adsorption investigations, which produced removal percentages of 86 % and 88 %, respectively, under specific conditions. The eco-friendly zinc oxide nanoparticles achieved maximum adsorption capacity and effective removal of methylene blue and crystal violet dyes under the following conditions: a pH value of 10, nanoparticle concentration of 0.06 g, reaction time of 50 min, dye concentration of 50 mg/L, and reaction temperature of 40 °C. Isotherm investigations demonstrated that the adsorption of methylene blue dye by eco-friendly zinc oxide nanoparticles followed the Temkin isotherm model, whereas the adsorption of crystal violet dye followed the Freundlich isotherm model. The kinetic parameters describing the adsorption of methylene blue and crystal violet dye onto eco-friendly zinc oxide nanoparticles were identified as pseudo-first-order and Elovich models, respectively. Following the above-mentioned studies, eco-friendly zinc oxide nanoparticles were subjected to additional characterization in order to assess their potential for wastewater treatment.

Intensified adsorption of chromium (VI) by catalpa-activated carbon from water and real electroplating industry wastewater

ABSTRACT In the present study, a novel adsorbent, activated carbon produced from the catalpa tree fruit was evaluated for adsorption of Cr (VI) from water and real electroplating wastewater. The batch adsorption experiments were conducted to investigate the impact of various operational variables, namely contact time, pH, initial concentration of Cr (VI), and the dose of activated carbon. Experimental data were used to determine the most suitable isotherm and kinetic models. The optimal values of the process were identified at a contact time of 150 min, a pH 2, an initial Cr (VI) concentration of 40 mg/L, and an adsorbent dose of 0.6 g/L that led to mean Cr (VI) removal of 95% with adsorption capacity (q) equal to 75 mg/g. The Langmuir isotherm and pseudo-first-order kinetic models could well explain the adsorption equilibrium. Furthermore, the thermodynamic analysis indicated that the adsorption process was characterised by exothermicity. The efficiency of the adsorbent in removing Cr (VI) from the real electroplating wastewater was obtained about 80%. However, the required adsorbent dose was 1.5 g/L. The fruit of the catalpa tree represents a cost-effective material for producing activated carbon, with a high capacity for adsorbing Cr (VI) from aqueous solution and wastewater.

Torrefaction of Cassia fistula seeds for sequestration of aqueous and gaseous pollutants: Experimental and computational approach

Contamination of water bodies due to pharmaceutical pollutants including antibiotics is growing day by day due to enhanced consumption of these molecules. Biochar is a competent material for wastewater treatment due to ease of preparation as well as high adsorption capability towards desired pollutants. Cassia fistula biochar (CFB) was prepared by torrefaction process in an inert atmosphere. Owing to a large surface area of 672.3 m2/g, the purpose of this work is to carry out adsorption studies of three antibiotics, namely, ciprofloxacin (CFX), levofloxacin (LVX) and diclofenac sodium (DFC) in aqueous phase as well as for the sequestration of carbon dioxide in gaseous phase. The batch adsorption studies were carried and effects of various operational conditions were studied. The maximum adsorption capacities for CFX, LVX, and DFC were found to be 607.86 mg/g, 68.27 mg/g and 160.51 mg/g respectively under the optimum pH 6.0 for all the three adsorbates, contact time of 60 minutes for CFX, LVX and 20 minutes for DFC at room temperature condition of 298 K. Various operational parameters were optimized using Response Surface Methodology (RSM). Isotherm and kinetics studies for the adsorption of all three drugs followed Langmuir model (R2 >0.99) and pseudo-second order kinetics (R2 >0.95). Thermodynamic studies show the adsorption of all three drugs were enthalpy driven spontaneous processes. Fixed bed studies were performed showing the applicability of CFB for larger sample volumes. DFT calculations showed strong attractive interaction of CFB with all the three drug molecules. The same material has been applied for capture of carbon dioxide at different temperatures. The CO2 capture studies showed maximum adsorption capacity of 64.78 cc/g at 273 K owing to activation of CFB with high CO2 selectivity of 14.29 with respect to nitrogen. Hence, a multipurpose adsorbent has been thoroughly studied with environmental sustainability factor of 0.03.

Unraveling the interplay of common groundwater ions in arsenic removal by sulfide-modified nanoscale zerovalent iron.

Sulphidation of nZVI (S-nZVI) has shown to significantly improve the arsenic removal capacity of nZVI, concurrently modifying the sequestration mechanism. However, to better apply S-nZVI for groundwater arsenic remediation, the impact of groundwater coexisting ions on the efficacy of arsenic uptake by S-nZVI needs to be investigated. This present study evaluates the potential of S-nZVI to remove arsenic in the presence of typical groundwater coexisting ions such as Cl-, HA, HCO3-, PO43- and SO42- through batch adsorption experiments. Individually, PO43- and HA had a dominant inhibition effect, while SO42- promoted As(III) removal by S-nZVI. Conversely, for As(V) removal, HCO3- and SO42- impeded the removal process. X-ray spectroscopic investigation suggests that the coexisting ions can either compete with arsenic for the adsorption sites, influence the S-nZVI corrosion rates and/or generate distinct corrosion products, thereby interfering with arsenic removal by S-nZVI. To investigate the cumulative effects of these ions, a 25-1 Fractional Factorial Design of experiments was employed, wherein the concentration of all the ions were varied simultaneously in an optimized manner, and their impact on arsenic removal by S-nZVI was observed. Our results shows that when these ions are present concurrently, PO43-, SO42- and HA still exerted a dominant influence on As(III) removal, whereas HCO3- was the main ions affecting As(V) removal, although the combined influence of the ions was not merely a summation of their individual effects. Overall, the finding of our study might provide valuable insight for predicting the actual performance of S-nZVI in field-scale applications for the remediation of arsenic-contaminated groundwater.

Adsorption characteristics and mechanisms of bisphenol A on novel nitrogen-modified biochar derived from waste masks and biomass.

Resource utilization of waste masks has become an urgent scientific issue. In this work, with sustainably, waste masks and biomass were co-pyrolysis with oxygen limitation to prepare mask-based biochar (MB). Then, urea was introduced to prepare novel nitrogen modified mask-based biochar (NMB) via a one-step hydrothermal synthesis method. The adsorption characteristics of NMB on the emerging environmental pollutant, bisphenol A (BPA), were evaluated via batch adsorption tests. Moreover, the physicochemical properties of the materials were characterized with various advanced techniques. Also, the roles of waste masks and nitrogen modification were explored. The adsorption mechanisms of NMB on BPA were revealed as well as the performance differences between different adsorbents. The results showed that waste masks participated in thermochemical reactions, shaped the microsphere structure of biochar, and increased the types of surface functional groups. The nitrogen modification enriched the surface elemental composition and activated the specific surface area via the mesopore. These would enhance the adsorption performance. The maximum adsorption of BPA by NMB was 62.63mg·g-1, which was approximately 2.35-5.58 times higher than that of the control materials. Temkin model and pseudo-second-order model optimally simulate the isothermal and kinetic adsorption, respectively. The adsorption mechanisms are jointly by physical and chemical adsorption, which mainly includes π-π interaction, hydrogen bonding, intraparticle diffusion, surface adsorption, and ion exchange. After discussion and evaluation, NMB has lower preparation process cost (7.21 USD·kg-1) and safety, with potential for environmental applications. This study aims to expand new ideas for the comprehensive utilization of waste masks and the preparation of eco-friendly materials. Moreover, it provides a theoretical basis for the removal of BPA.

Synthesis of eco-friendly bio-based coconut shell magnetic biochar for efficient bisphenol S sequestration in aqueous environment: green technology breakthrough

Water pollution has emerged as a critical global challenge, particularly the contamination of water bodies with persistent organic pollutants such as Bisphenol S (BPS), a known endocrine disruptor. This study presents the synthesis and application of eco-friendly bio-based coconut shell magnetic biochar (CSMB) for efficient sequestration of BPS from aqueous environments. Utilizing pyrolysis and co-precipitation techniques, the magnetic biochar was characterized through various methods including surface chemistry (pHpzc), electron dispersive X-ray analysis (EDX), Brunauer-Emmett-Teller (BET) N2 adsorption-desorption, scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), and Fourier transform infrared spectroscopy (FTIR). SEM revealed a porous structure with a high surface area, while FTIR confirmed the presence of functional groups essential for adsorption. X-ray diffraction (XRD) and VSM successfully incorporated magnetic nanoparticles, enhancing the separation process post-adsorption. The CSMB demonstrated a significant surface area of 373 m2 g−1, outperforming regular coconut shell biochar (CSB), with a BPS adsorption capacity of 43.5 mg/g compared to 26.7 mg/g for CSB. Batch adsorption tests assessed the impact of operational factors such as initial BPS concentration (8–150 ppm), contact time (30–150 min), temperature (298.15, 318.15, and 338.15 K), pH (3–11), and CSMB dosage (0.1–0.9 g). The results indicated optimal adsorption at pH 6 with a maximum capacity of 52.3 mg/g. Kinetic studies revealed that the pseudo-second-order model best described the adsorption process, while the Langmuir isotherm model provided an excellent fit for the adsorption data. The reusability of CSMB was validated over five cycles, with adsorption capacity decreasing slightly from 43.5 mg/g to approximately 41 mg/g, making it a sustainable and effective adsorbent for water treatment.

Fabrication of low-cost magnetic Kaolin/Graphene oxide nanocomposites for oil droplet removal from oil-in-water emulsions: batch adsorption experiments

Fabrication of low-cost magnetic Kaolin/Graphene oxide nanocomposites for oil droplet removal from oil-in-water emulsions: batch adsorption experiments

Enhanced adsorption of Congo red dye by CS/PEG/ZnO composite hydrogel: Synthesis, characterization, and performance evaluation

Hydrogels are 3D interconnected network polymer chains that are hydrophilic, swell in water and imbibe a significant amount of water. When hydrogel absorb water, dye molecules transfer to their surface, aiding adsorption. Adsorption is efficient, cheap, and versatile technique to remove dye from aqueous media. In this study, high-performance adsorbents from chitosan/polyethylene glycol (CS/PEG) hydrogel cross-linked with intermolecular H-bonds and chitosan/polyethylene glycol/ZnO (CS/PEG/ZnO) composite hydrogel cross-linked with Zn2+ were developed by an instantaneous gelation method. The prepared composite hydrogels were characterized by Fourier transform infrared (FTIR) spectroscopy, Scanning electron microscopy (SEM), X-ray diffraction (XRD), thermo-gravimetric analysis (TGA), transmission electron microscopy (TEM) and Zeta-sizer. The developed composite hydrogels effectively adsorbed Congo red (CR) dye from aqueous media. CR adsorption efficiency using adsorbent dosage, contact time, pH and temperature factors were conducted by batch adsorption experiments. The obtained results for CR adsorption equilibrium were compatible with the Langmuir model with maximum adsorption capacity (qmax) of 212.76 mg/g for CS/PEG and 256.41 mg/g for CS/PEG/ZnO composite hydrogel. The qmax was measured at pH 3 and 25 min and kinetic study confirmed that pseudo 2nd order kinetic model was best followed. Thermodynamic study indicated that the nature of the adsorption phenomena was physical, endothermic and spontaneous. The high adsorption efficiency is mainly ascribed to the protonation of –NH2 groups present in CS/PEG and CS/PEG/ZnO composite hydrogels which enhanced its electropositivity. Hydrogen bond formation and electrostatic attraction among adsorbent and dye govern the adsorption mechanism. It can be concluded that CS/PEG hydrogel and CS/PEG/ZnO composite hydrogels could be considered as efficient, beneficial and potential adsorbents for environmental remediation.