Thermodynamic Analysis Research Articles

On the Valorization of Olive Oil Pomace: A Sustainable Approach for Methylene Blue Removal from Aqueous Media.

Currently, industrial water pollution represents a significant global challenge, with the potential to adversely impact human health and the integrity of ecosystems. The continuous increase in global consumption has resulted in an exponential rise in the use of dyes, which have become one of the major water pollutants, causing significant environmental impacts. In order to address these concerns, a number of wastewater treatment methods have been developed, with a particular focus on physicochemical approaches, such as adsorption. The objective of this study is to investigate the potential of a bio-based material derived from olive oil pomace (OOP) as an environmentally friendly bio-adsorbent for the removal of methylene blue (MB), a cationic dye commonly found in textile effluents. The biobased material was initially characterized by determining the point of zero charge (pHpzc) and using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). Subsequently, a comprehensive analysis was conducted, evaluating the impact of specific physicochemical parameters on MB adsorption, which included a thorough examination of the kinetic and thermodynamic aspects. The adsorption process was characterized using Langmuir, Freundlich, Brunauer-Emmett-Teller (BET), and Dubinin Radushkevich (D-R) isotherms. The results suggest that the equilibrium of adsorption is achieved within ca. 200 min, following pseudo-second-order kinetics. The optimal conditions, including adsorbent mass, temperature, bulk pH, and dye concentration, yielded a maximum adsorption capacity of ca. 93% (i.e., 428 mg g-1) for a pomace concentration of 450 mg L-1. The results suggest a monolayer adsorption process with preferential electrostatic interactions between the dye and the pomace adsorbent. This is supported by the application of Langmuir, BET, Freundlich, and D-R isotherm models. The thermodynamic analysis indicates that the adsorption process is spontaneous and exothermic. This work presents a sustainable solution for mitigating MB contamination in wastewater streams while simultaneously valorizing OOP, an agricultural by-product that presents risks to human health and the environment. In conclusion, this approach offers an innovative ecological alternative to synthetic adsorbents.

Ecofriendly Dyeing Strategy Based on Dyeing Kinetics and Thermodynamic Analysis for Melt-Spun Polyurethane Fibers.

Melt-spun polyurethane fibers (MSPUFs) have garnered popularity owing to efficient production methods and exceptional stability. However, the development of the MSPUF has been restricted by challenges such as poor dyeability as well as energy and cost concerns associated with the dyeing process. Herein, we devised a highly efficient dyeing technique that operates at a lower temperature and a shorter duration. In comparison to conventional dyeing methods, our novel approach reduces the temperature from 98 to 75 °C, while reducing the amount of dye utilized by 25% and the dyeing time by 50%. In this method, the modifier increases both the positive charge and the amorphous zone of the fiber, while rational dyeing conditions are designed based on thermodynamic and kinetic analyses. This strategy enabled a 76.3% increase in E% and a 45.9% increase in K/S values at reduced temperatures and a shorter time while simultaneously improving the dye-fiber bonding fastness. This research methodology not only enhances the dyeing performance of MSPUF but also reduces energy consumption and dyeing costs, presenting an ecofriendly and economically novel approach for the development of dyeable MSPUF.

Kinetic and thermodynamic analysis of alizarin Red S biosorption by Alhagi maurorum: a sustainable approach for water treatment

Synthetic dyes, such as Alizarin Red S, contribute significantly to environmental pollution. This study investigates the biosorption potential of Alhagi maurorum biosorbent for the removal of Alizarin Red S (ARS) from aqueous solutions. Fourier transform infrared spectroscopy (FTIR) was used to analyze the biosorbent’s adsorption sites. Various parameters were optimized to maximize dye adsorption. An optimal removal efficiency of 82.26% was attained by employing 0.9 g of biosorbent with a 25 ppm dye concentration at pH 6 and 60 °C over 30 min. The data were modeled using various isothermal and kinetic models to understand the adsorption behavior. Thermodynamic parameters indicated that the adsorption process was spontaneous and endothermic. The pseudo-second-order kinetic model best described the data, indicating chemisorption as the rate-limiting step. The data matched best to the Langmuir model, indicating that the adsorption occurs as a monolayer on uniform surfaces with a finite number of binding sites. The model showed a strong correlation (R² = 0.991) and a maximum adsorption capacity (qmax) of 8.203 mg/g. Principal component analysis (PCA) identified temperature as the dominant factor, with the primary component, PC1 capturing 100% of its effect. The mechanisms involved in ARS biosorption on A. maurorum include electrostatic interactions, hydrogen bonding, hydrophobic interactions, dipole-dipole interactions, and π-π stacking. Alhagi maurorum showed promising potential for biosorbing toxic dyes from contaminated water, suggesting further investigation for practical applications.

Phase equilibria and thermodynamic analysis of liquid–liquid immiscibility in the system SiO2–Na2O–MoO3

AbstractPhase equilibrium experiments were carried out in the SiO2–Na2O–MoO3 system at 1200ºC and 1000ºC. We found that immiscible phase region in this system is narrower than that reported previously. By combining phase relationship and thermodynamic data and assuming associate species model, interaction parameters to describe enthalpy of mixing of SiO2–Na2O–MoO3 liquid were optimized by CALPHAD methodology. The thermodynamic database can be applied to thermodynamic calculations of silicate systems containing molybdenum, such as the vitrification process of high-level radioactive waste.

Corrosion Inhibition and Adsorption Behaviour of Centrosema pubescens Leaf Extract for Copper in HCl Solution

Study’s Excerpt In this study, Centrosema pubescens leaf extract (CPE) has been confirmed as eco-friendly and efficient green inhibitor for copper corrosion in hydrochloric acid. Detailed thermodynamic analysis, revealed that CPE adsorption follows a Freundlich isotherm model. SEM-EDX and FTIR characterizations confirmed the formation of a protective layer confirming the potentials of the plant extracts in sustainable corrosion prevention. Full Abstract The anti-corrosion behaviour of Centrosema pubescens leaf extract (CPE) on copper in 1.5 M hydrochloric acid was investigated using weight loss method at different temperatures, followed with scanning electron microscopy (SEM) surface characterization connected with energy dispersive X-ray spectroscopy (EDX). The Fourier transform infrared spectrum of CPE was obtained. CPE inhibition effectiveness depends on the temperature and its concentration. CPE restrains the copper corrosion with 94.26 % inhibition efficiency at 1.0 g/L of CPE and at 303 K. For the CPE-inhibited system, a higher activation energy (Ea) value (range of 31.09 to 38.70 kJmol-1) compared to 20.34 kJmol-1 of the blank solution was obtained. The reaction process is spontaneous and endo thermic, as indicated by the ΔH, ΔS and ΔG values calculated. CPE adsorption behaviour fitted best into Freundlich isotherm.

Developing alkali-activated controlled low-strength material (CLSM) using urban waste glass and red mud for sustainable construction

Using industrial waste in controlled low-strength material (CLSM) offers many benefits and addresses waste management issues. However, identifying optimal CLSM design while balancing environmental impacts and engineering properties poses a notable challenge. Herein, new alkali-activated CLSM formulations based on urban waste glass and red mud (RM) are proposed for the first time with systematic investigations into the material properties and sustainability. The formulations involve the ternary blends of slag, glass powder (GP) and RM as the binders and crushed glass as aggregate. Our observations show RM has a clay-like texture with complex crystalline phases rich in Al and Fe. Increasing the proportion of RM to GP notably decreases the flowability, extends the setting time and impairs the mechanical properties. Nevertheless, red mud demonstrates a crucial role of reducing bleeding level especially for the mixtures with high proportions of glass aggregate. The standard leachate tests as per toxicity characteristic leaching procedure (TCLP) show the heavy metals leached from the CLSM are below the concentration limits and exhibit low mobility. The microstructural and thermodynamic analyses reveal the precipitation of calcium-(sodium-)aluminosilicate hydrate (C-(N-)A-S-H) as the major binding material. The reactive Fe and Al in red mud most probably contribute to the formation of hydrogarnet phases. Moreover, the suggested CLSM formations typically exhibit reduced carbon emissions and lower costs compared to the traditional CLSM produced with cement and fly ash, underlining their environmental sustainability and cost-effectiveness. This study provides a potential guideline for the flowable fill construction in the regions with bauxite producers.

Evaluating Ammonia and Methanol as Lower-Emission Alternatives to liquefied natural gas for Medium-speed Marine Engines: A Thermodynamic Analysis

Evaluating Ammonia and Methanol as Lower-Emission Alternatives to liquefied natural gas for Medium-speed Marine Engines: A Thermodynamic Analysis

Co‐Pyrolytic Recycling of Bakelite and Polymethyl Methacrylate: Kinetic, Synergistic, and Thermodynamic Analysis

AbstractBakelite, a thermosetting plastic, has limited feasibility for thermal recycling processes such as pyrolysis, unlike thermoplastics, due to its inherent tendency to get charred upon heating and difficulty in being converted into valuable fuel and chemical compounds. In this study, the co‐pyrolysis of bakelite and poly methyl methacrylate is explored to improve the thermal degradation and thus recycling feasibility of bakelite by pyrolysis. The kinetics and thermodynamics of the co‐pyrolysis of blended samples are analyzed using different kinetics models. The thermal degradation experiments of the sample are conducted from ambient to 1000 °C at five various heating rates of 5, 10, 20, 30, and 50 °C/min in an inert N2 gas environment. The results showed that adding poly methyl methacrylate to bakelite changes the pyrolytic degradation temperature and weight loss trend. The kinetic analysis reveals that the thermal degradation at 220–345 °C follows an F2.5 order‐based model with an average activation energy of 181 kJ/mol, while the degradation at 345–475 °C follows an F2 order‐based model with an average activation energy of 318 kJ/mol. The enthalpy changes and free energy change associated with thermal degradation exhibit a positive trend while that of entropy change shows a negative trend. With blending the free energy change and entropy change decreased while enthalpy change increased. During batch pyrolysis at 450 °C, the PMMA‐Bakelite blend generates oil (49.17 %), wax (12.36 %), residue (15.36 %), and gas (23.11 %). According to FTIR and GC‐MS analyses, the pyrolytic oil produced by the co‐pyrolysis of the blended sample at 450 °C comprises 32.23 % saturated hydrocarbons (C9–40), 20.97 % unsaturated hydrocarbons (C6–24), and 46.80 % oxygenated material (C5–19). These findings can assist in the optimization of pyrolysis reactor design for the recycling of thermosetting plastics.

Pressure induced tunable physical properties of cubic KHgF3 fluoro-perovskite: A first principle study

The structural, electronic, optical, mechanical, and thermodynamic properties of KHgF3 perovskite under various hydrostatic pressures are examined in this study in the frameworkof Density Functional Theory (DFT) with the Generalized Gradient Approximation (GGA) Perdew-Burke-Ernzerhof (PBE) exchange–correlation function. Tunable physical properties have been observed in KHgF3 as pressure is incrementally applied. The investigated compound displays mechanical instability beyond the pressure range of 0 to –10 GPa, as confirmed by the elastic constant analysis. Under ambient pressure, the lattice constants of KHgF3 closely align with theoretically calculated values, affirming the accuracy of this investigation. In addition, the bandgap of KHgF3 narrows with increasing pressure, facilitating easier electron transition from the valence band to the conduction band. The study reveals that when subjected to different hydrostatic pressures, fluctuations are observed in the peaks of the conductivity spectrum, loss spectrum, and absorption spectrum, particularly shifting towards higher photon energies, as analyzed through the optical properties. Moreover, KHgF3 exhibits ductile behavior at 0 GPa pressure, and this ductility rises with pressure. Thermodynamic analysis reveals a decrease in Debye temperature with increasing pressure, while the melting temperature rises correspondingly. The findings of this investigation also imply that KHgF3 can be a good candidate for optoelectronic device application under different hydrostatic pressures.

Oxidative Aromatization of Ethane

This study is focused on examining the incorporation of oxidative dehydrogenation into the aromatization of ethane, utilizing thermodynamic analysis and catalytic experiments. The catalysts were characterized by inverse temperature programmed reduction, X‐ray photoelectron spectroscopy (XPS) and X‐ray diffraction (XRD). The results indicated that a blend of the M1 catalyst, containing oxides of vanadium, niobium, and tellurium, with H‐ZSM‐5, serves as an effective catalyst system for the oxidative aromatization of ethane at T = 380 °C. The M1's role in the oxidative dehydrogenation of ethane contributes to de‐bottlenecking the essential step of the reaction. On the zeolitic catalyst aromatic compounds are formed from a surface hydrocarbon pool. In parallel, the oxidation of these intermediates was observed. Also, the formation of paraffins through H‐transfer was evident from the catalytic results. While the zeolite underwent significant deactivation due to coking, the M1 catalyst demonstrated highly stable activity. Interestingly, the system did not show any synergistic effects. Based on the structure‐activity relation of the catalytic system a reaction mechanism is proposed.

Heat Pump-Assisted Extractive Pressure-Swing Distillation with Integrated Feed Preconcentration/Solvent Recovery for Isopropanol-Benzene-Water Separation

Recently, heat-integrated pressure-swing distillation (HIPSD) has been explored for recovering isopropanol and benzene from wastewater, but the process remains highly energy-intensive. Given the dilute nature of the feed, intensified extractive distillation with an integrated preconcentration column (IED) is more suitable. However, previous researches have often overlooked the critical role of pressure and lacked rigorous optimization of operating pressure in such systems. In this article, we developed novel extractive pressure-swing distillation with integrated feed preconcentration/solvent recovery column (IEPSD) by introducing a pressure-swing configuration and incorporate energy-saving technologies to achieve more sustainable and cost-effective separation processes. First, thermodynamic analysis is conducted to explore the effect of pressure on extractive pressure-swing distillation. Then, a parallel genetic algorithm is applied for rigorous optimization, followed by the application of heat integration and heat pump. The IEPSD is superior to IED in terms of total annual cost (TAC) and CO2 emission. With the inclusion of energy-saving technologies, IEDHI and IEPSDHI further reduced TAC by 5.29% and 7.40%, and cut CO2 emissions by 25.18% and 24.03%, respectively, compared to their base processes. The use of a heat pump is particularly advantageous for IEPSD due to its lower boiling temperatures under vacuum pressure, leading to the development of IEPSDHIHP, which offered an additional 22.36% CO2 reduction and marginally lower TAC than IEPSDHI. Ultimately, IEPSDHIHP proves to be the best option, offering a 51.15% TAC reduction and 68.42% CO2 emissions reduction compared to HIPSD. In summary, the developed IED and IEPSD processes, especially with heat integration and heat pump technologies, offer significant economic and environmental advantages over conventional HIPSD.

Adsorption of Pb(II) and Cd(II) on Modified Coal Gasification Slag: Competitive Adsorption, Leaching Toxicity, and Adsorption Mechanism

AbstractTo remove heavy metals from wastewater, coal gasification slag (CGS) was prepared as an adsorbent. Five modified materials were created, including HF‐CGSC, KOH‐HCl‐CGS, and three KOH‐CGS variants with different mass ratios. The adsorption tests showed KOH‐CGS (0.25) had the best efficiency for Pb(II) and Cd(II) via spontaneous chemisorption. Kinetic, thermodynamic, and 13C NMR analyses indicated that adsorption involved pore adsorption, functional group coordination, and π‐π interactions. Competitive adsorption results showed minimal interaction between Pb and Cd. Leaching tests confirmed the process's environmental safety. This study suggests new approaches for using coal gasification slag in wastewater treatment.

Investigation of the iridium adsorption process with functionalized magnetic nanoparticles using triisobutylphosphine sulfide extractors

In this research work, the adsorption process of iridium using magnetic nanoparticles functionalized with Cyanex 471X has been investigated. In this regard, parameters affecting the adsorption process such as pH, initial concentration of iridium ions, contact time and adsorbent dosage were assessed. According to the results, pH 6, adsorbent dosage 1.2 g/L, initial concentration of iridium of 10 mg/L, and contact time of 10 min were selected as optimal conditions for iridium adsorption by this synthesized magnetic nanosorbent. The kinetics of the adsorption process was studied, and it was found that the adsorption reaction follows the pseudo-second-order kinetic model with the correlation coefficient of 0.9960. Also, experimental studies indicated that the Langmuir adsorption isotherm model best matches the experimental data (R2 = 0.9961). The maximum adsorption capacity of the nanosorbent for iridium adsorption was estimated to be 35.34 mg/g by the Langmuir isotherm. With the thermodynamic analysis of the adsorption process, it was found that this process is endothermic and spontaneous. In addition, in the investigation of iridium adsorption and desorption, HCl/HNO3 solution with a concentration of 1.5 M was selected as suitable eluent.

Enhancing Adsorption Performance of Ce(III) by Amine-Thiourea and Aniline-Modified Magnetic Chitosan Nanocomposites.

To enhance the adsorption performance of chitosan for rare earth ions, two novel magnetic chitosan-based adsorbents were prepared by using chitosan-coated magnetic silica nanoparticles modified with amine-thiourea and aniline. The structure of copolymers was analyzed using characterization methods such as X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and thermogravimetric analysis, confirming the successful synthesis of modified magnetic chitosan nanocomposites. The investigation explored the influence of pH, contact time, dosage, initial concentration, and temperature on the adsorption performance. Comparative studies revealed a significantly enhanced adsorption performance after modification. The chitosan-coated magnetic silica nanoparticles modified with aniline (PAN-CS/Fe3O4@SiO2) reached adsorption saturation in about 120 min with a capacity of 136 mg/g, while the chitosan-coated magnetic silica nanoparticles modified with amine-thiourea (TSC-CS/Fe3O4@SiO2) exhibited a higher adsorption capacity of 156 mg/g for Ce(III). Both materials demonstrated strong agreement with the Langmuir isotherm model and pseudo-second-order kinetics. Thermodynamic analysis indicated that Ce(III) adsorption is both spontaneous and endothermic. Examination of the adsorption mechanisms suggested that the effective adsorption of Ce(III) is due to the strong synergistic effects of chelation and electrostatic interactions involving amino, carboxyl, and hydroxyl groups. This study demonstrates that chitosan modified with amine-thiourea and aniline is an effective approach to significantly enhance the rare earth ion adsorption by chitosan.

Mechanism of Thermodynamically Rationalized Selective Growth of a Two-Dimensional Ternary Ferromagnet on Insulating Substrates.

Two-dimensional (2D) semiconducting ferromagnet Fe3GeTe2 holds great promise for advanced spintronic applications because of its gate-tunable ferromagnetic ordering at room temperature, whereas the controllable growth of large-area single crystals remains very challenging due to its ternary nature and variable stoichiometry inducing many competitive phases. Here, we theoretically probe the mechanism of selective growth of monolayer Fe3GeTe2 on various epitaxial substrates. Thermodynamic analysis shows that the corresponding phase-pure chemical potential windows for the selective growth of Fe3GeTe2 can be reasonably attained in ternary phase space on insulating and chemically inert c-plane sapphire and Ga2O3(0001) substrates by properly modulating the interfacial interaction and employing suitable feedstocks to avoid competitive growth of possible impurity phases with different stoichiometry ratios. It is also revealed that both the weak edge-substrate interaction and interlayer coupling of Fe3GeTe2 together lead to a surface-dominated nucleation behavior and, thereby, energetically favor lateral growth of the monolayer rather than vertical growth of the multilayer. Importantly, straight protocols for the experimentally selective growth of phase-pure ternary Fe3GeTe2 are also provided by establishing the relationship between the feedstock chemical potential and growth parameters on a thermochemical basis. Our insightful study can also be reasonably extended to guide future experimental design for the selective growth of other multicomponent 2D materials.

Thermodynamic analysis of a novel compressed carbon dioxide energy storage coupled dry methane reforming system with integrated carbon capture

Chemical absorption CO2 capture, compressed carbon dioxide energy storage (CCES) and dry reforming of methane (DRM) can be used for continuous carbon capture, storage and utilization. However, CO2 capture is often accompanied by significant energy consumption. Considering the waste high-grade thermal energy at the exit of solar methane reforming, the article proposes a coupled system in which the thermal energy at the exit of the DRM system is used in CCES to improve the system's work capacity, and the remaining heat and the compression heat of the CCES are used for CO2 capture. The study established mathematical models of the three subsystems, performed thermodynamic analyses, and completed experiments on dry reforming of methane. The results show that the coupled system can increase the electro-electric conversion efficiency by 150.49 % reaching 220.33 % and the energy efficiency by 7.25 % reaching 77.09 %. The coupled system can save up to 43.33 % of CO2 capture heat. The DRM subsystem can utilize the higher temperature CO2 in the tail end of the CCES system, and its methane conversion efficiency and solar-fuel efficiency can be increased by 3.54 % and 3.20 % respectively to reach 58.22 % and 61.02 %. And the economic analysis found that the coupled system has better economics.

Effective purification of Fe/V as spherical phosphosiderite and porous vanadium oxyhydroxide from waste vanadium-bearing slag

Recovery of valuable vanadium (V) from V-rich waste was of economic and environmental and commonly treated by calcination and/or extraction. Herein, a novel route was developed to stepwise separate Fe and V from grayish slag via a coupled dissolution and hydrothermal route. After dissolving the V-rich slag in acid, the generated leachate was hydrothermally treated with the addition of phosphate and ethanol. 99.1 % Fe was effectively removed, whilst the loss of V and Mg were only 5.2 % and <2 %. The optimal parameters were 160 °C, 20 g/L phosphate and 0.1-ml ethanol. Fe reacted with phosphate and crystallized as phosphosiderite particles at 160 °C. With the Fe removal, free H+ was released and then consumed in the redox reaction of nitrate and ethanol. The thermodynamic analysis showed that phosphate accelerated the Fe hydrolysis/crystallization, resulting in the removal of Fe prior to V at the pH < 0.5 and the co-removal of Fe/V at the pH > 1. 98.7 % V was recycled as vanadium oxide hydrate particles by adjusting the leachate to pH 0.2 at 90 °C by adding urea. This provided as a promising strategy to separate Fe and V from leachate and posed potential application in the resource utilization of V-rich waste.

Molecular Dynamics Simulation Study on the Structural and Thermodynamic Analysis of Oxidized and Unoxidized Forms of Polyaniline.

The conducting polymer polyaniline (PANI) has shown significant interest for the development of electrified membranes (EMs) with superior antifouling characteristics. However, the blending and doping of PANI with other polymers and nanomaterials highly influence the properties of the membrane surface. PANI exists in two forms: oxidized, known as emeraldine salt (ES), and unoxidized, referred to as emeraldine base (EB). Therefore, understanding the different forms of PANI and the variations between the oxidized and unoxidized forms along the length of the polymer chain is intriguing. In this paper, we present the design of a novel copolymer consisting of EB and ES monomers with varying charge densities and different segmental arrangements. We present various intra- and intermolecular structural properties of the PANI chains using all-atom molecular dynamics (MD) simulations. Herein, we present a detailed conformational free energy analysis to understand the conformational transitions of the PANI chains. Our results show increased radius of gyration (Rg) values with increased charge density. Furthermore, we also present the H-bonding, free energy analysis, reduced density gradient (RDG), and solvent-accessible surface area (SASA) values for the observed conformational transitions of PANI. Therefore, these observations are crucial in understanding the complex behavior of chains for designing target-specific polymeric materials.

High-performance activated carbon from coconut shells for dye removal: study of isotherm and thermodynamics.

This study investigates the production of high-performance activated carbon (AC) from coconut shells (CS) through acid and base activation processes, along with pre- and post-functionalization of the biochar, aiming to effectively remove dyes from aqueous solutions. The resulting AC exhibited outstanding adsorption capabilities, with the Langmuir model providing a good fit to the experimental data. Maximum adsorption capacities were observed at different temperatures: 805 mg g-1 at 298 K, 904 mg g-1 at 318 K, and 1000 mg g-1 at 338 K for NaOH-activated AC, and 252 mg g-1 at 298 K, 295 mg g-1 at 318 K, and 305 mg g-1 at 338 K for H2SO4-activated AC. The presence of active sites and functional groups on the surface of AC facilitated dye adsorption. The influence of various parameters, including adsorbent dosage, dye concentration, pH, and temperature, on the adsorption process were also examined, identifying the ideal conditions for dye removal. Thermodynamic analysis confirmed the endothermic nature of the adsorption process, with higher temperatures leading to increased adsorption capacities. Overall, the research highlights the potential of various activation routes for the production of high-value AC as a sustainable and effective adsorbent for dye removal from wastewater.

Investigation of the biological removal of nickel and copper ions from aqueous solutions using mixed microalgae

AbstractThe use of mixed microalgae offers an effective solution for the management of contamination risks in cultivation while enhancing economic viability. In this study, mixed microalgae were used for the first time for the removal of copper (Cu) and nickel (Ni) from aqueous solutions. The characteristics of the adsorbents were examined thoroughly, and the adsorption process was assessed using isotherms, kinetics, and thermodynamics. Particle size, concentration, contact time, temperature, and pH were among the variables assessed. The findings demonstrated that, at an initial concentration of 100 mg L–1 and a pH of 6, the maximum adsorption of Cu with a particle size of 1 mm (90.20%) took place in 60 min. The highest adsorption rate (78.25%) was found for Ni. Microalgae performed best over 180 min at room temperature and at pH values that promoted metal dissolution. The removal percentages of wet and dried microalgae were comparable, and the wet adsorbent was more economical. It was feasible to remove both metals at the same time. Up to three cycles of adsorbent reuse were possible, with sodium hydroxide treatment offering superior removal to hydrochloric acid. Thermodynamic analysis demonstrated that this process, which results in a disordered state, is exothermic and spontaneous.