Elovich Models Research Articles

Preparation and characterization of β-cyclodextrin capped magnetic nanoparticles anchored on cellulosic matrix for removal of cr(VI) from mimicked wastewater: Adsorption and kinetic studies

Hexavalent Chromium (Cr(VI)) is essential in many industrial processes. However, it finds its way into water bodies, posing health problems, including lung cancer and the inhibition of DNA and RNA in biological systems. Several chemical and traditional water purification methods have been developed in the past, but most are expensive, tedious and ineffective. This study aimed to prepare and characterize a low-cost hybrid adsorbent, β-Cyclodextrin capped magnetic nanoparticles anchored on a cellulosic matrix (CNC-Fe3O4NP-CD). The characterization techniques confirmed the integration of CNCs, Fe3O4NP and CD into the prepared CNC-Fe3O4NP-CD nanocomposite adsorbent. The adsorbent was employed in batch adsorption experiments by varying adsorption parameters, including solution pH, adsorbent dosage, initial Cr(VI) concentration, and contact time. From the findings, the nanocomposite adsorbent achieved a maximum Cr(VI) removal efficiency of 97.45%, while the pseudo-second-order kinetic model best fitted the experimental data with high linear regression coefficients (R2 > 0.98). The Elovich model indicated that the adsorption process was driven by chemisorption on heterogeneous surface sites, with initial sorption rates surpassing desorption rates. These findings established that CNC-Fe3O4NP-CD presents high efficiency for Cr(VI) removal under acidic pH, offering the potential for optimization and application in real-world wastewater treatment.

Eco-friendly property modulation of biobased gels of carboxymethyl cellulose-integrated poly(tertiary amine)s for the removal of azo-food dyes

Anionic polysaccharide-based gels enable the design of biobased materials with biochemical properties, non-toxic and natural origin. A new set of cationic gels was prepared from carboxymethylcellulose (CMC)-doped tertiary amino functional cationic monomers 2-(dimethylamino)ethyl methacrylate and N-(3-(dimethylamino)propyl) methacrylamide via the formation of semi-interpenetrated network (semi-IPN) at different polymerization temperatures, Tprep. A detailed understanding of the temperature-dependent synthesis and physicochemical response is required for the design of interpenetrating networks with CMC as an adsorbent that provides effective sources for the removal of azo-food dyes such as tartrazine and carmoisine from aqueous solutions. The variation of elasticity and swelling properties with respect to polymerization temperature was investigated. CMC-integration and polymerization temperature played a decisive role in the compressive elasticity. Incorporation of CMC into copolymer matrix led to a significant increase in elasticity of semi-IPNs, while mechanically weaker gels were obtained with increasing Tprep. Addition of CMC increased the swelling modulus of semi-IPNs formed at −18 °C by 2.6-fold. While the transparency changed depending on Tprep and microstructure, addition of CMC decreased the swelling rate of gels at all polymerization temperatures. The compressive modulus decreased with the swelling process in accordance with the Rubber elasticity theory. Semi-IPN gels showed stable swelling against pH-change in aqueous solutions and exhibited excellent pH-sensitivity significantly in low pH. A 4 to 12 fold decrease in maximum volume was observed by varying the pH between 2.1 and 9.8. The correlation between polymerization temperature and removal of azo-food dyes; tartrazine and carmoisine from contaminated wastewater with CMC-based gels was studied. Dynamic adsorption equilibrium was reached in 30 min, and tartrazine and carmoisine removal performances varied between 92.8 % and 98.4 %. respectively. The adsorption data for azo-dyes were evaluated by Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Redlich-Patterson, Sips, and Tooth isotherm models, but were best described by Langmuir and Redlich-Patterson models as they gave the highest correlation. Pseudo-first order, pseudo-second order, Elovich, Avrami kinetic and intra-particle diffusion models were investigated and dye adsorption was represented by pseudo-second-order model. After the adsorption process, semi-IPNs can easily be regenerated and effectively reused over five cycles. The study provided new insights towards the facile and sustainable synthesis of eco-friendly multifunctional CMC-based gels carrying tertiary amino groups for effective removal of azo-based food colorants.

Comprehensive study on copper adsorption using an innovative graphene carbonate sand composite adsorbent: Batch, fixed-bed columns, and CFD modeling insights

This study focused on an innovative graphene carbonate sand composite adsorbent, synthesized from carbonated porous sand and sucrose as raw materials, for the removal of copper ions via the adsorption process. The characteristics of this adsorbent are determined through comprehensive experiments and numerical simulations in batch and fixed-bed column conditions, which has not been extensively explored. Extensive experimentation demonstrated a remarkable 100 % removal efficiency under optimal conditions, which included a copper ion concentration of 3 g/L, a contact time of 10 h, and an adsorbent dosage of 35 g/L. The adsorption kinetics and isotherm results exhibited that the Elovich model (R² = 0.998) and the Langmuir model (R² = 0.996 for linear with qm=123.91 mg g-1, and R² = 0.993 for nonlinear fitting) more effectively described the adsorption of copper onto the adsorbent. In the fixed-bed column studies, among the well-known analytical models, the Log-Gompertz model showed better compatibility (R2 = 0.97∼0.99) between breakthrough curves with experimental results for various copper inlet concentrations. Also, numerical results obtained using computational fluid dynamics and mass transfer simulations with the linear driving force model were successfully validated by experimental results, particularly in the initial and transition zones of the breakthrough curve.

Construction and demolition waste as a low-cost adsorbent for water treatment: kinetics, isotherm, thermodynamics, and Fenton regeneration.

The present study proposes to investigate the feasibility of using construction and demolition waste (CDW) as an aqueous remediation agent through adsorption. The CDW, with and without chemical and thermal pre-activation, was evaluated to remove the methylene blue (MB) dye from the water solution. Variables interfering with adsorption processes, such as adsorbent dosage, solution pH, and particle size, were evaluated. The material was characterized by pHZPC, FTIR, XRD, SEM, EDS, and TG. The kinetic and equilibrium data better fitted the Elovich and Sips models, respectively. A maximum adsorption capacity of 18.62mgg-1 at 60°C was observed. Thermodynamic data indicated that adsorption occurred through a spontaneous and favorable process governed mainly by physical processes. The regeneration studies were carried out using processes based on the Fenton reaction, where the catalytic action of the iron naturally present in the CDW was evaluated. The results showed that the desorption balance was the main limiting factor for the effective regeneration of the saturated material. Adding Fe2+ to the system made this process suitable for the regeneration of the CDW and degradation of the pollutant in the aqueous phase. A regeneration efficiency of 65%, maintained practically constant during five adsorption-regeneration cycles, was observed. These results highlight the high potential of using CDWs as an adsorbent material.

Highlighting the adsorption mechanism of a fluoroquinolone antibiotic from wastewater on carbon xerogel by experiments, characterization, modelling and DFT simulation.

The application of a synthesized carbon xerogel (RFX) for the adsorptive removal from water of ciprofloxacin (CPX), a widely used fluoroquinolones-group antibiotic for humans and animals, has been reported in this work. The carbon xerogel was characterized by N2 adsorption-desorption isotherms, FTIR, Raman spectroscopy, TPD studies, elemental analysis, determination of isoelectric point (pHIEP) and scanning electron microscopy (SEM). CPX adsorption experiments were conducted in batch mode, using results obtained with F400 commercial activated carbon for comparison purposes. CPX adsorption kinetics were well-described by the pseudo-second-order model for both adsorbents and by the Elovich model in the case of F400 activated carbon. Therefore, CPX equilibrium adsorption capacity values were of 457 and 72mgg-1 for RFX xerogel and F400 activated carbon, respectively. This significant difference can be attributed to the higher specific surface area and micropores volume values of F400 carbon; in this sense, this material led to a slower CPX kinetic adsorption. Also, the Dual-site Langmuir model best-described the experimental CPX adsorption isotherms in both cases. By the adsorption studies at different solution pH, it could be concluded that several mechanisms, e.g., hydrophobic and π-π interactions, and electrostatic forces highly influenced CPX adsorption capacity. Furthermore, adsorption tests using several environmentally relevant aqueous matrices have been accomplished. In this case, a competitive effect between the natural organic matter (NOM) and the target pollutant occurred in all the tested real matrices, decreasing CPX adsorption capacity, especially remarkable for F400 activated carbon. Finally, Density Functional Theory (DFT) has been used to elucidate the interactions between CPX and adsorbents, finding a high relevance of the π-π electron donor-acceptor interactions in which CPX acts as an acceptor.

Kinetic and Mechanistic Analysis of Phenol Adsorption on Activated Carbons from Kenaf

Activated carbons were prepared from kenaf (Hibiscus cannabinus L.). Carbonization was carried out at 600 °C for 2 h, and activation was performed using air at 600 °C and using CO2 at 750 °C. The activated carbons obtained were treated with HNO3 and H2SO4. The samples were characterized by their chemical and physical structure. The activated carbons obtained were mainly macroporous, and their structure underwent major changes with the activation method and acid treatment. Activated carbons were alkaline and acid-treated carbons were neutral. They were used for phenol adsorption and a kinetic and mechanistic study of adsorption was carried out. The fit to the pseudo-second order and Elovich models was predominant. The rate-limiting step of the process was determined to be diffusion within the pores, as the experimental data fit the Bangham model. DFT simulation showed that the preferred adsorption position involves π-π stacking and that oxidation enhances this interaction. Furthermore, the simulation showed that the interaction of phenol with oxygenated functional groups depends on the type of functional group.

A Sustainable Solution for the Adsorption of C.I. Direct Black 80, an Azoic Textile Dye with Plant Stems: Zygophyllum gaetulum in an Aqueous Solution.

The presence of pollutants in water sources, particularly dyes coming by way of the textile industry, represents a major challenge with far-reaching environmental consequences, including increased scarcity. This phenomenon endangers the health of living organisms and the natural system. Numerous biosorbents have been utilized for the removal of dyes from the textile industry. The aim of this study was to optimize discarded Zygophyllum gaetulum stems as constituting an untreated natural biosorbent for the efficient removal of C.I. Direct Black 80, an azo textile dye, from an aqueous solution, thus offering an ecological and low-cost alternative while recovering the waste for reuse. The biosorbent was subjected to a series of characterization analyses: scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET) method, X-ray diffraction (XRD), and infrared spectroscopy (IR) were employed to characterize the biosorbent. Additionally, the moisture and ash content of the plant stem were also examined. The absorption phenomenon was studied for several different parameters including the effect of the absorption time (0 to 360 min), the sorbent mass (3 to 40 g/L), the pH of the solution (3 to 11), the dye concentration (5 to 300 mg/L), and the pH of the zero-charge point (2-12). Thermodynamic studies and desorption studies were also carried out. The results showed that an increase in plant mass from 3 to 40 g/L resulted in a notable enhancement in dye adsorption rates, with an observed rise from 63.96% to 97.08%. The pH at the zero-charge point (pHpzc) was determined to be 7.12. The percentage of dye removal was found to be highest for pH values ≤ 7, with a subsequent decline in removal efficiency as the pH increased. Following an initial increase in the amount of adsorbed dye, equilibrium was reached within 2 h of contact. The kinetic parameters of adsorption were investigated using the pseudo-first-order, pseudo-second-order and Elovich models. The results indicated that the pseudo-first-order kinetic model was the most appropriate for the plant adsorbent. The isotherm parameters were determined using the Langmuir, Frendlich, Temkin, and Dubinin-Radushkevich models. The experimental data were more satisfactory and better fitted using the Langmuir model for the adsorption of dye on the plant. This study demonstrated that Zygophyllum gaetulum stems could be employed as an effective adsorbent for the removal of our organic dye from an aqueous solution.

Biochar-based fertilizers from co-pyrolysis of algae and hazelnut shell with triple superphosphate: Physicochemical properties and slow release performance.

Phosphorus (P) is a vital nutrient for plant growth and food production. Excessive amounts of P fertilizers to a greater extent of crop P offtake are inevitably applied due to low utilization efficiency, causing environmental pollution. This study aimed to evaluate biochar-based fertilizers (BBFs) produced by co-pyrolyzing algae (A) and hazelnut shell (H) biomasses with triple superphosphate (TSP) at a ratio of 4:1 (w/w). The potential of the slow-release performance of BBFs was studied during kinetics experiments. The co-pyrolysis of biomasses with TSP yielded BBFs with significantly different properties, including electrical conductivity, pH, elemental ratios, functional groups, specific surface area and pore size characteristics. Phosphorus release from all biochars and BBFs followed the Elovich model, except for TSP and H+TSP. Kinetic studies revealed prolonged P-release times and slower release rates for BBFs compared to conventional TSP. So that, TSP released 100% of the total P, whereas H+TSP and A+TSP biochars released only 3.14% and 5.14% of the total P, respectively, during a 240-hour experiment. The slow-release performance of BBFs suggests their potential as promising alternatives to conventional phosphate fertilizers. BBFs have the potential to enhance P utilization efficiency, increase crop yield and mitigate the environmental impact of P fertilizer runoff.

Food dye adsorption in single and ternary systems by the novel passion fruit peel biochar adsorbent

This study evaluated the passion fruit peel biochar (PFPB) as a novel adsorbent for synthetic food dyes indigotine blue (IB), tartrazine yellow (TY), and ponceau 4R (P4R) removal in single and ternary systems. A macroporous structure and a predominance of basic groups characterized PFPB. The pH study revealed better adsorption at pH 2.0. The response surface methodology optimization for adsorbent dosage and temperature predicted removal efficiencies of 100 % for IB, 79.8 % for TY, and 84.4 % for P4R. Elovich and Redlich-Peterson models better described kinetic and equilibrium, respectively, suggesting the contribution of chemical interactions. Thermodynamic data revealed endothermic, with an inordinate degree and spontaneous adsorption. In the ternary systems, antagonistic effects of interaction were noticed. The adsorption of synthetic effluents showed promising results with removal efficiencies of 99.6 % (IB), 60.2 % (TY), and 51.8 % (P4R). Therefore, we concluded that PFPB is a potential alternative low-cost synthetic food dye removal adsorbent.

Performance study of phenol sequestration from agricultural wastewater by chemical activated Montmorillonite

Agricultural by-products possess potential as cost-effective adsorbents for the remediation of phenolic contaminants in environmentally treated wastewater. This research focuses on the utilization of Algerian montmorillonite clay, specifically modified montmorillonite (Mo-5N), treated with 5N hydrochloric acid (HCl), compared to its untreated form (Mo-0N), for phenol sequestration from pesticide-laden waters. We employed various analytical techniques, such as chemical analysis, X-ray diffraction (XRD), and Fourier Transform Infrared (FTIR) spectroscopy, to characterize these adsorbents. The adsorption behavior was scrutinized under varying conditions, including pH, contact time, phenol concentration, and temperature. The maximum adsorption capacities achieved were 119.12 mg/g for Mo-5N and 100.89 mg/g for Mo-0N under optimal conditions of pH 5.72, a contact time of 120 minutes, and a temperature of 40°C. The kinetics of adsorption were best described by the pseudo-second-order and Elovich models, while the Freundlich isotherm model aptly described the equilibrium data. Thermodynamic analyses revealed that the phenol removal process using both forms of montmorillonite is spontaneous and endothermic. This study demonstrates the efficacy of Algerian montmorillonite clay in the removal of phenolic pesticides from agricultural wastewater.

Use of Chitosan-Iron Oxide Gels for the Removal of Cd2+ Ions from Aqueous Solutions.

High-quality water availability is substantial for sustaining life, so its contamination presents a serious problem that has been the focus of several studies. The presence of heavy metals, such as cadmium, is frequently studied due to the increase in the contamination levels caused by fast industrial expansion. Cadmium ions were removed from aqueous solutions at pH 7.0 by chitosan-magnetite (ChM) xerogel beads and chitosan-FeO (ChF) xerogel beads in batch systems. Kinetic studies were best modeled by the Elovich model. The adsorption isotherms obtained showed an inflection point suggesting the formation of a second layer, and the BET model adjusted to liquid-solid systems was adequate for the description of the experimental data. Maximum uptake capacities of 36.97 ± 0.77 and 28.60 ± 2.09 mg Cd/g xerogel were obtained for ChM and ChF, respectively. The studied composites are considered promising adsorbent materials for removing cadmium ions from aqueous systems.

Sensor parameters and adsorption behaviour of rhodamine-based polyacrylonitrile (PAN) nanofiber against dichloromethane vapour

This study is focused on the determination of sensor and adsorption parameters ofrhodamine-based polyacrylonitrile (PAN) nanofiber during the dichloromethane vapour exposure due to a very limited investigation of the rhodamine-based PAN nanofiber sensor. Quartz crystal microbalance (QCM) measurement system is employed to monitor the sensor response to dichloromethane vapour. This nanofiber sensor demonstrates a highly sensitive, stable, reproducible response and concentration dependence behaviour. A good stability, with an excellent recovery occurred. Sensor parameters such as the limit of detection (153 ppm), the limit of quantification (465 ppm), the sensitivity (0.0215 Hz/ppm), response (2 s) and recovery (3 s) times are determined using QCM measurement results. Pseudo first-order and Elovich adsorption models have proved that dichloromethane vapours are adsorbed bythis nanofiber sensor andthe amount of vapour adsorption rate is increased when the concentration of dichloromethane vapour increases.Owing to its achieved sensor parameters, high adsorption feature and simple fabrication process with a low cost, this proposed sensing device is expected to be a promising alternative for monitoring dichloromethane vapour sensing application at room temperature.

Application of Anionic Hydrogels from Date Palm Waste for Dye Adsorption in Wastewater Treatment.

This work aimed to develop an anionic cellulose nanofiber (CNF) bio-adsorbent from date palm tree waste and to investigate its removal efficiency compared to cationic methylene blue dye from contaminated water. Date palm pulp was first prepared from date palm leaves through acid hydrolysis using H2SO4, followed by hydrolysis in a basic medium using KOH, in which the process completely removed the components of hemicellulose, lignin, and silica. To obtain anionic CNF, the resulting pulp was further treated with H2SO4, followed by centrifugation. Biogel formation of the CNF suspension was promoted by sonication, where its removal efficiency of methylene blue dye was studied as a function of dye concentration, temperature, contact time, and pH value. In this work, we investigated two isotherms, i.e., Langmuir and Freundlich. The Langmuir model's consistency with the experimental data suggests that the adsorption of methylene blue dye onto CNF is monolayer and surface-limited. The reported maximum removal efficiency of 5 mg/g at 60 °C indicates the optimal temperature for adsorption in this specific case. Additionally, a pseudo-second-order model and Elovich model were also utilized to obtain a better understanding of the adsorption mechanism, in which we found not just physical adsorption but also an indication of a chemical reaction occurring between methylene blue dye and CNF. According to the results, that pseudo-second-order model's consistency with the experimental data suggests that the adsorption of methylene blue (MB) onto CNF is rate-limiting step involving chemisorption between the two. The study reveals that CNF adsorbents derived from renewable natural waste sources such as date palm leaves can be effective in removing cationic contaminants such as methylene blue dye.

Enhanced Tetracycline Adsorption Using KOH-Modified Biochar Derived from Waste Activated Sludge in Aqueous Solutions.

Antibiotic pollution poses a serious environmental concern worldwide, posing risks to ecosystems and human well-being. Transforming waste activated sludge into adsorbents for antibiotic removal aligns with the concept of utilizing waste to treat waste. However, the adsorption efficiency of these adsorbents is currently limited. This study identified KOH modification as the most effective method for enhancing tetracycline (TC) adsorption by sludge biochar through a comparative analysis of acid, alkali, and oxidant modifications. The adsorption characteristics of TC upon unmodified sludge biochar (BC) as well as KOH-modified sludge biochar (BC-KOH) were investigated in terms of equilibrium, kinetics, and thermodynamics. BC-KOH exhibited higher porosity, greater specific surface area, and increased abundance of oxygen-based functional groups compared to BC. The TC adsorption on BC-KOH conformed the Elovich and Langmuir models, with a maximum adsorption capacity of 243.3 mg/g at 298 K. The adsorption mechanisms included ion exchange, hydrogen bonding, pore filling, and electrostatic adsorption, as well as π-π interactions. Interference with TC adsorption on BC-KOH was observed with HCO3-, PO43-, Ca2+, and Mg2+, whereas Cl-, NO3-, and SO42- ions exhibited minimal impact on the adsorption process. Following three cycles of utilization, there was a slight 5.94% reduction in the equilibrium adsorption capacity, yet the adsorption capacity remained 4.5 times greater than that of unmodified sludge BC, underscoring its significant potential for practical applications. This research provided new insights to the production and application of sludge biochar for treating antibiotic-contaminated wastewater.

A systematical comparation of Cu (II) adsorption behavior and mechanism between biomass fly ash and biogas residue pyrolysis char

Biomass fly ash (BFA) and biogas residues are the main by-products of biomass direct-fired power generation and biogas production. This study compares the Cu(II) adsorption mechanisms of BFA and biogas residue pyrolysis char (BRPC) through systematic tests. BFA exhibited a significantly higher adsorption capacity (75.34 mg/g) than BRPC (42.80 mg/g). The pseudo-first-order kinetic model best described BFA, while the Elovich model was optimal for BRPC. Both materials fit the Freundlich isotherm model. BFA's superior mineral co-precipitation and ion-exchange capacity are due to its rich mineral content, particularly calcium. BRPC benefits from an additional functional group complex adsorption due to its pyrolytic charcoal content. Variations in pore structure of BFA and BRPC did not demonstrate a significant effect on the adsorption. The results of this study provide essential data support for the potential of high-value utilization of BFA and BRPC and the innovative modification of high-performance biomass-based heavy metal adsorbent materials.

Assessment of the Effects of ZnO and CuO Engineered Nanoparticles on Physicochemical Properties of Volcanic Ash Soil and Phosphorus Availability

The presence of engineered nanoparticles (ENPs) in soil systems can modify their properties and the availability of nutrients. This study evaluated the effect of 1% CuO or ZnO ENPs on the physicochemical properties and on the phosphorus (P) adsorption–desorption processes of a volcanic ash soil (Lautaro; LAU). The dynamics of P were conducted through kinetic and isotherm batch experiments. The results showed that LAU soil with 1% CuO or ZnO ENPs increased pHH2O (from 5.67 to 6.03 and 6.82, respectively), electrical conductivity (from 0.119 to 0.143 and 0.150 dS m−1, respectively), Zn availability (597.7 times higher for LAU with 1% ZnO ENPs in relation to soil without ENPs), and Cu availability (41.8 times higher for LAU with 1% CuO ENPs in relation to soil without ENPs). Moreover, the presence of ENPs decreased Brunauer, Emmett, and Teller specific surface area. The adsorption kinetic studies of P on LAU soil without and with 1% ENPs fitted well to the Elovich model (r2 ≥ 0.923), which indicated a chemiadsorption mechanism, whereas the adsorption isotherms were described by Langmuir–Freundlich model (r2 ≥ 0.939). The desorption percentage was LAU > LAU + 1% CuO–ENPs > LAU + 1% ZnO–ENPs, demonstrating an increased stability of the P–soil surface binding with 1% ENPs. Co–existing NO3−, SeO42−, and SO42− anions did not generate a steric hindrance between P and LAU soil binding. Finally, both ENPs could alter the quality of the soil due to changes in their physicochemical properties and decrease the availability of P in volcanic ash soils.

A detailed practical and theoretical study of the adsorptive potential of synthesised ceria impregnated activated graphite for aqueous Se(IV) and Te(IV) removal: Process optimisation, characterisation and mechanistic approach

A cost-effective, simple, and earth friendly nanocomposite adsorbent was synthesized by in - situ penetration of ceria nanocrystals on graphite to remove aqueous selenium (IV) and tellurium (IV). Batch experiments optimize parameters such as pH, temperature, sorbent dosage and equilibration time of 30 minutes. The adsorbent exhibited the maximum adsorption capacities of 144.5 mg/g for Te(IV) and 29.3 mg/g for Se(IV). BET analysis revealed a specific surface area of 16.44 m²/g, an average pore diameter of 4.24 nm, and a high pore volume of 0.0519 cm³/g. The adsorbent was characterized before and after adsorption by SEM-EDX, XRD and FTIR. The sorption data could be well interpreted by the Langmuir model for both Se and Te and by the DR isotherm for Te(IV) at ambient temperature. Kinetic empirical data correlated positively with pseudosecond order for both Se and Te and the Elovich model for Te at room temperature. Kinetics and equilibrium isotherms suggested that the adsorption occurred through surface adsorption using electrostatic bonding along with physisorption involving steady diffusion and accommodation of analyte ions into mesopores and defects of the adsorbent. Chemisorption by electron transfer of the oxyanions of Se/Te with Ce3+/Ce4+ of the cerium impregnated graphite (CIAG) and ion exchange with functional groups on the activated graphite edges were other probable mechanisms. The adsorbent demonstrated the ability to be regenerated and reused over multiple cycles, with minimal interference from coexisting ions emphasizing its selectivity. All measurements were conducted in triplicate with the relative standard deviation (RSD) below 5 %. The optimised method was successfully applied in natural water samples from various sources, demonstrating strong potential for scaling up to field applications.

Performance Evaluation of a Romanian Zeolite: A Sustainable Material for Removing Ammonium Ions from Water

Ammonium ion is a chemical species that is found in abundance in natural waters, whether underground or surface, but also in wastewater resulting from agricultural and industrial activities. Even if the removal of the ammonium ion from water has been studied for a very long time, it has been found that its removal is far from being solved. In this study, we evaluated the performance of the ammonium ion adsorption process on two adsorbents, zeolite clinoptilolite, ZR, a sustainable material (manufacturer: Zeolite Development SRL, Rupea, Brasov, Romania), and the other granular activated carbon type, Norit GAC 830 W. Zeolite ZR is found in very large deposits in Romania; it is a natural, cheap material with costs between 50 and 100 EUR/ton, compared to other adsorbents that cost over 500 EUR/ton and which can be regenerated and reused in the technological process of water treatment and purification, but also after exhaustion, as an amendment for the soil. In the first step, this paper presents the mineralogic (XRD) and structural (SEM and EDX) characterization of the ZR and the determination of the pH zero-point charge, pHZPC, for all the adsorbents. Studies were carried out in equilibrium and kinetic conditions. The efficiency of the adsorbent was investigated in different experimental conditions by varying the initial concentration, particle size, temperature, pH, ionic strength, and contact time. The mathematical models and parameters specific to the adsorption isotherms that best describe the experimental results were identified. Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich mathematical models were used for comparison. The Langmuir isotherm proved to be the most appropriate to describe the adsorption of ammonium ions on all types of adsorbents used. The adsorption capacity of ammonium ions from synthetic solutions at 20 °C, pH = 6.09, for the range of initial concentrations 0–50 mg/L for Rupea zeolite is in the range of 10.46 mg/g−12.34 mg/g, and for granular activated carbon GAC W830, it is 16.64 mg/g. It was found that the adsorption capacity of the ammonium ion on both activated carbon and zeolite increases with increasing temperature and pH. Also, it was observed that as the ionic strength increases, the adsorption capacity decreases for all four adsorbents. Kinetic models were also identified that best describe the experimental processes. In this sense, pseudo-first order, pseudo-second order, intra-particle diffusion and the Elovich model were used. The results of the investigation showed that second-order kinetics governs the adsorption process on ZR, and pseudo-first order governs activated carbon.

Fabrication of nanozeolite-Y/chitosan composite based on rice husks for efficient adsorption of methylene blue dye: kinetic and thermodynamic studies

In this work, three solid adsorbents were synthesized, namely, nanozeolite-Y prepared from rice husks ash by a sol-gel method as a green biosource (ZN), chitosan as a cationic biopolymer (CS), and nanozeolite-Y/chitosan composite (CSZ). An eco-friendly composite that consists of chitosan and nanozeolite-Y was used to combine the advantages of nanoparticles with biopolymers two materials to increase the removal % of methylene blue dye. All the synthetized solid adsorbents were investigated using TGA, nitrogen adsorption, SEM, TEM, FTIR, XRD, and zeta potential. The results showed that CSZ particles had a high specific surface area (432.3 m2/g), mesoporosity (with an average pore diameter of 2.59 nm), a smaller TEM particle size (between 28.6 and 60.7 nm), a lot of chemical functional groups, and high thermal stability. CSZ exhibited the maximum adsorption capacity (141.04 mg/g) towards methylene blue. The adsorption nature of methylene blue onto CS and CSZ is endothermic, spontaneous, and a physical adsorption process, while it is exothermic, nonspontaneous, physical adsorption process in the case of ZN, as confirmed by thermodynamic results. Pseudo-second order, Elovich, Dubinin-Radushkevich, Freundlich, Langmuir, Temkin, and adsorption models all fit the MB adsorption well, with correlation coefficients reaching about 0.9997. Nitric acid was found to be the best desorbing agent, with a desorption efficiency of about 99%.

Adsorptive removal of diclofenac on nanoporous anoxic sewage sludge biochar: Investigating the influence of carbonization temperature, residence time and specific Fe(III) infusion

This study explores the removal of the emerging contaminant diclofenac using pristine biochar and iron-impregnated biochar derived from anoxic sewage sludge. A biochar ensemble was prepared at varying pyrolysis temperatures (350 °C to 950 °C) and residence times (30 to 240 min). The iron-modified material was synthesized by incorporating FeCl3 with the precursor at 950 °C for 30 min. A comprehensive characterization based on the morphology, crystallinity, and functional groups confirmed the structural and chemical modifications in the pristine and modified biochar of interest. Adsorption experiments demonstrated that iron-modified biochar exhibited superior adsorption capacity for diclofenac (18.958±0.417 mg/g) compared to pristine biochar (0.814±0.001 mg/g), attributable to its larger surface area and more active sites. The adsorption mechanisms were identified as a combination of electrostatic interactions, hydrogen bonding, and complexation, with significant Fe3+ to Fe2+ reduction indicating electron transfer processes. Adsorption kinetics followed the Elovich model, and equilibrium studies fitted best to the Redlich-Peterson model for the iron-amended biochar. The study also assessed the reusability of the adsorbents, with pristine and iron-impregnated biochar maintaining around 70 % removal efficiency up to 3 and 5 cycles, respectively. Consequently, both the biochar serve as potentially efficient adsorbents for diclofenac removal from aqueous solutions.