Thermodynamic Studies Research Articles

Extraction of Anacardium occidentale: a kinetic, thermodynamic, phytochemical identification, and antibacterial study

Cashew tree biomass, Anacardium occidentale, represents an underutilized part of the plant and could have great potential for application in several areas, such as bioengineering, food science, and chemical. The stirred bed process was optimized to produce extracts from Anacardium occidentale stem bark (SBAo) and leaves (LAo) for bactericide purposes. Variables as alcohol content, stirring speed (SS), particle size (PS), solid-to-solvent ratio (S/S), temperature, and extraction time were evaluated. Subsequently, kinetic, thermodynamic and diffusivity fittings of the data were performed using different nonlinear models (Peleg, 2nd order, Elovich, power law, and Fick’s 2nd law) applied to the yield curves. Extracts were characterized by Fourier-transform infrared (FTIR) spectroscopy, total phenolic content (TPC), total flavonoid content (TFC), trolox equivalent antioxidant capacity (TEAC), and ultra-high resolution mass spectrometry (UHRMS) techniques for qualitative and quantitative determination of the phytochemicals. The optimized operating conditions obtained were ethanol in solvent at 70%, PS < 45 μm, 1200 rpm SS, 1/10 S/S ratio, and extraction time of 1 h at 50 ºC. The 2nd order kinetic model was the one that presented the best fits: SBAo (R2 > 0.9893 and RMSE < 3.4293) and LAo (R2 > 0.9985 and RMSE < 3.1117). Both A. occidentale extracts showed high levels of polyphenols and flavonoids, such as anacardic acid. Finally, the optimized extracts showed antibacterial susceptibility, with larger halos against S. aureus, 0.88± 0.07 mm (SBAo) and 0.45 ± 0.03 mm (LAo), in relation to E. coli, 0.80 ± 0.10 mm (SBAo) and 0.69 ± 0.08 mm (LAo).

CALPHAD modeling of [formula omitted]- carbide dual ordering in Fe-Al-C ternary alloys

A novel four-sublattice model for the κ phase, denoted as (Fe, Al)3(Fe, Al)1(C, Va)1(C, Va)3 was proposed to improve the thermodynamic prediction, such as equilibrium composition, phase stability of κ-carbide in Fe-Al-C system. The sublattice model explains the transformation from the disordered FCC solid solution to the ordered κ-carbide via concurrent ordering of substitutional and interstitial atoms. The dual ordering model can restrict the irregular contribution of configurational entropy arising at 20 at% C composition, which is an issue with the existing thermodynamic databases. For the CALPHAD assessment, κ-carbide was considered as a single, individual phase that is in equilibrium with the liquid, austenite (γ), ferrite (α) or other intermetallic and carbide phases in the Fe-Al-C system. The formation energy calculated from density functional theory (DFT) showed that Fe3Al–L12 phase is energetically more favorable than the Fe3AlC–E21 phase, and C atoms in sublattice IV are not energetically favorable at all. The assessed parameters provided better accuracy than the existing database in the calculations of isothermal sections, liquidus projection, invariant reactions, and low-temperature phase compositions. The model is highly suitable for the low temperature (<800 °C) phase predictions. Thus, the improved Fe-Al-C model lays the foundation for the thermodynamic and kinetic studies of κ-carbide for designing new Fe-Mn-Al-C alloys and optimizing the heat treatment processes.

Modified gum ghatti based hybrid hydrogel nanocomposite as adsorbent material for dye removal from wastewater

A hybrid hydrogel nanocomposite based on the polysaccharide-gum ghatti, has been made and evaluated as an adsorbent material for wastewater treatment. The nanocomposite is composed of a network of gum ghatti-graft-poly(2-acrylamido-2-methylpropane sulfonic acid) with magnetite nanoparticles embedded within. This functional material Ggh-g-PAMPS/Fe3O4 has been characterized by FTIR, TGA, SEM, EDS, XRD, BET and VSM techniques. The presence of magnetite nanoparticles imparted superparamagnetic property to the adsorbent material enabling its easy separation after use with an external magnet. The characterization data indicated mesoporous nature of the nanocomposite adsorbent with mean pore diameter of 4.9 nm. The nanoparticles imparted high surface area to the adsorbent material the value being 4.7 m2g−1 based on nitrogen adsorption experiments. The suitability of the material as an adsorbent for removal of cationic dyes from water was checked with two cationic dyes namely, rhodamine 6G and methylene blue. The maximum adsorption capacity of the nanocomposite Ggh-g-PAMPS/Fe3O4 towards rhodamine 6G and methylene blue were observed to be 403.2 and 427.8 mg g−1 respectively from their individual solutions of concentration 500 mg L−1. The pH dependence on swelling and surface charge indicated medium of pH of 7.0 as the ideal condition for effective adsorption. Freundlich isotherm model and pseudo second order kinetic model are observed to be the most befitting models to describe adsorption. Further, the thermodynamic studies revealed the adsorption to be a spontaneous and endothermic process. The desorption study portrayed the reusability of the adsorbent material. The excellent adsorption performance and magnetic nature of the developed nanocomposite suggests its potential application as an adsorbent material in wastewater treatment.

Enhancement of Trihalomethane Adsorption Capacity Using Chitosan-Modified Coconut Shell Activated Carbon: Adsorption Characteristics and Mechanisms

There is a rising concern about the safety risk that trihalomethanes (THMs) in drinking water pose. In this work, to adsorb THMs such as chloroform (TCM), dibromochloromethane (DBCM), bromodichloromethane (BDCM), and bromoform (TBM), we coated chitosan (CS) on coconut shell activated carbon (CAC). The adsorbents were characterized using BET, XRD, FTIR, and SEM techniques. The impact of various variables was examined, including contact time, quantity of adsorbent, initial pH, and initial THM concentrations. Under the same conditions, TCM was adsorbed most efficiently, followed by BDCM, DBCM, and TBM. When the pH was between 4 and 8, the adsorption of THMs onto the coconut shell activated carbon supported chitosan (CS/CAC) varied relatively little; however, when the pH increased above 8, the adsorption of THMs decreased. For THMs, CS/CAC adsorption was a chemical reaction and monolayer adsorption that fit better with the pseudo-second-order kinetic model and the Langmuir isotherm model. According to the thermodynamic study, THMs were adsorbed endothermically and spontaneously on CS/CAC. For column experiments, the adsorption of THMs was influenced by bed height and flow rate. After up to four cycles of adsorption and desorption, it was found that the adsorbent was reusable. The maximum adsorption capacities for Langmuir were 187.27, 114.29, 93.28, and 89.61 µg/g for TCM, BDCM, DBCM, and TBM, respectively. CS/CAC has a high adsorption capacity, especially for TCM, which is responsible for a major portion of THMs in drinking water. This indicates that CS/CAC has a lot of potential uses when it comes to removing THMs from water.

Enhanced adsorption of malachite green onto a composite material activated carbon and iron(III) oxide nanoparticles: isotherm, kinetic, and thermodynamic study

Enhanced adsorption of malachite green onto a composite material activated carbon and iron(III) oxide nanoparticles: isotherm, kinetic, and thermodynamic study

Design and utilisation of a novel poly imino-phosphorane composite for the effective removal of Pb2+ and Cr3+ ions from contaminated water sources

ABSTRACT This study introduces a novel chitosan-immobilised imino-phosphorane composite (Chi-iph) for the efficient removal of lead (Pb2+) and chromium (Cr3+) from wastewater. The successful synthesis of Chi-iph was confirmed using FT-IR, XPS, BET, EDX, TGA, 1H-NMR, 13C-NMR, EI/MS, and ICP-OES analyses. Various experimental parameters such as pH, equilibrium time, metal concentration, adsorbent dose, temperature, and eluents were optimised to enhance the adsorption performance. At 25°C, with pH values of 5.5 for Pb2+ and 4.5 for Cr3+, an initial concentration of 200 mg/L, and an agitation time of 20 min, the maximum adsorption capacities were 55 mg/g for Pb2+ and 45 mg/g for Cr3+. Kinetic modelling demonstrated that the pseudo-first-order model best predicted the adsorption process, yielding capacities of 56.65 mg/g for Pb2+ and 46.38 mg/g for Cr3+. Isotherm analysis showed that the Langmuir model was a better fit than the Freundlich model, with theoretical capacities of 56.81 mg/g for Pb2+ and 44.64 mg/g for Cr3+. The Dubinin–Radushkevich (D-R) isotherm revealed adsorption energy (E) values of 9.45 kJ/mol for Pb2+ and 8.64 kJ/mol for Cr3+, indicating a chemisorption process. Theoretical saturation capacities (qD) were 56.28 mg/g for Pb2+ and 45.58 mg/g for Cr3+. Temkin isotherm results, with bT values of 9.71 and 8.53 kJ/mol for Pb2+ and Cr3+ respectively, aligned closely with the D-R model, further confirming chemisorption. Thermodynamic studies indicated that the adsorption process is exothermic, spontaneous, and more favourable at lower temperatures. Complete desorption of the heavy metals was achieved using 1 M HNO₃, allowing for efficient metal recovery. In a practical application, the Chi-iph composite removed 11.5 mg/L of Pb2+ and 7.01 mg/L of Cr3+ from contaminated wastewater, demonstrating its potential for environmental remediation. The composite’s performance aligns with WHO and FAO guidelines, making it suitable for treating wastewater before disposal into marine environments.

Thermodynamic study on the phase assemblage of MPC exposed to natural and accelerated carbonation conditions

AbstractMagnesium phosphate cement (MPC), which belongs to chemically bonded phosphate ceramics, is commonly applied as a repair material and waste stabilization/solidifications. However, studies on the influence of CO2 on the phase assemblages in MPC are limited. A thermodynamic simulation approach is employed to explore the influence of CO2 on the equilibrium phase assemblage of MPC. The mechanisms of natural and enforced carbonation of MPC have been investigated in this work. The results disclose that Mg carbonates are less likely to precipitate in magnesium ammonium phosphate cement (MAPC) cured under CO2, while MgCO3·3H2O is the only carbonation product of magnesium potassium phosphate cement (MKPC). The carbonation resistance of MAPC is better than that of MKPC. The increase of activity of magnesia employed in MPC obviously enhances the formation of brucite and slightly promotes the carbonation of MPC.

Application of a magnetic graphene nanocomposite modified with 5-aminoisophthalic acid amine group for chromium (VI) adsorption from aqueous solutions: kinetic and thermodynamic studies

ABSTRACT Polymer nanocomposites are composite materials that incorporate nanomaterials, such as magnetic graphene oxide (mGO), into a polymer matrix. To enhance its adsorption capacity, the surface of mGO nanoparticles was polymerised by a 5-aminoisophthalic acid amine group (mGO-AIPA) through a simplified co-precipitation method. The structural and morphological characteristics of the synthesised nanoparticles were evaluated through techniques such as X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy (FESEM), Thermogravimetric analysis (TGA), and Vibrating sample magnetometer (VSM). Response surface method (RSM) was used to evaluate the effectiveness of mGO-AIPA nanocomposite in removing chromium (VI) ions by examining variables such as solution of pH, contact time, adsorbent dose and initial concentration. Also, the study of kinetic models, adsorption isotherms and thermodynamic modelling of the process were evaluated. The results found that the mGO-AIPA nanocomposite has the maximum removal of chromium (VI) ions from the aqueous solution by 83.11% in optimal conditions including pH 3.5, contact time of 35 min, an adsorbent dosage of 25 mg g−1 and an initial concentration of 55 mg L−1. The pseudo-second-order kinetic and Langmuir isotherm models had a better fit with the experimental data of adsorption and the maximum adsorption capacity of chromium (VI) the base of the Langmuir model was 90.91 mg g−1. Moreover, the thermodynamic analysis indicated that the process was exothermic and nonspontaneous process, implying that it was energetically unfavourable. These findings suggest that the mGO-AIPA nanocomposite has a high performance as an effectual adsorbent to eliminate chromium heavy metal from an aqueous medium.

Simultaneous Adsorption of Ampicillin and Lead by a Highly Stable UiO-66-NH2/TiO2 Nanocomposite from Water: Mechanism, Kinetics, Equilibrium, Thermodynamics, and Regeneration Studies

Simultaneous Adsorption of Ampicillin and Lead by a Highly Stable UiO-66-NH₂/TiO₂ Nanocomposite from Water: Mechanism, Kinetics, Equilibrium, Thermodynamics, and Regeneration Studies

Solubility of Sulfamerazine in Acetonitrile + Ethanol Cosolvent Mixtures: Thermodynamics and Modeling

Sulfamerazine (SMR) is a drug used as an antibacterial agent in the treatment of some pathologies, such as bronchitis, prostatitis and urinary tract infections. Although this drug was developed in 1945 and, due to its toxicity, was partially displaced by penicillin, due to the current problem of bacterial resistance, compounds such as SMR have regained validity. In this context, the thermodynamic study of SMR in cosolvent mixtures of acetonitrile (MeCN) + ethanol (EtOH) at nine temperatures (278.15–318.15 K) is presented. The solubility of SMR was determined by UV–Vis spectrophotometry, following the guidelines of the shake-flask method. The solubility process was endothermic in all cases; thus, the minimum solubility was reached in pure EtOH at 278.15 K, and the maximum solubility was reached in pure MeCN at 318.15 K. Both the solution process and the mixing process were entropy-driven. On the other hand, the solubility data were modeled by using the van’t Hoff–Yalkowsky–Roseman model, obtaining an overall average relative deviation of 3.9%. In general terms, it can be concluded that the solution process of SMR in {MeCN (1) + EtOH (2)} mixtures is thermodependent, favored by the entropy of the solution and mixture; additionally, the van’t Hoff–Yalkowsky–Roseman model allows very good approximations to be obtained and is a simple model that starts from only four experimental data.

Methylene Blue Adsorption Using Boric Acid Functionalized Activated Carbon: Kinetics, Isothermal, and Thermodynamic Studies

AbstractIn this study, the activated carbon (AC) was prepared from Sesbania sesban plant stem. Boric acid (H3BO3) was used as an activating agent. During calcination, the optimized temperature was kept upto 500 °C for 2 h. The prepared adsorbents were characterized using various techniques such as FT‐IR, scanning electron microscopy, energy dispersive x‐ray spectroscopy, and thermogravimetric analyzer. The prepared adsorbents were used for the removal of methylene blue (MB) dye adsorption. The adsorption experiments were conducted at different pHs such as (2–11), doses (0.0025–0.020 mg), times (30–300 min), MB initial concentrations (100–600 mg L−1), and temperatures (298–318 K), respectively. The maximum MB uptake capacity of the prepared adsorbent was 1380 mg g−1 under optimized adsorption conditions. Furthermore, the kinetic study is well described by pseudo‐second order, whereas the isothermal study showed the Freundlich isotherm was better followed by the equilibrium data. Based on thermodynamic studies, the negative values of ΔG° and ΔH° revealed that the MB adsorption process is spontaneous and exothermic in nature. However, the negative ∆Sxg° value indicates that solid‐solute interaction decreased randomness in the adsorption systems. The overall studies of AC showed that it was better to remove MB from an aqueous solution.

Development and assessment of a biomass-based energy system for green steel production: A thermodynamic study

ABSTRACT Steel is the fundamental pillar of contemporary society, given its significant greenhouse gas emissions, rapid transformation is required for deep decarbonization of the iron and steel industry. This paper proposes a strategy to generate green steel through the H2-DRI-EAF (Hydrogen direct reduced iron processed in an electric arc furnace) process, leveraging biomass as the primary feedstock. The proposed configuration contains a biomass gasifier to generate hydrogen, which is further used in a shaft furnace to reduce iron ore and is fed to an electric arc furnace to produce Green Steel. India serves as the focal point for this study, with agricultural residue from the four most abundant crops selected as the primary feedstock. With these chosen feedstocks, the system demonstrates the capacity to produce approximately 0.1 kg of hydrogen per kg of biomass. Operating with an overall energy efficiency of 29.2% and exergy efficiency of 41.4%, the plant exhibits a crucial characteristic: the ability to seamlessly integrate different feedstocks without significantly affecting its overall performance. The aim of the current study is to promote bioenergy as a viable pathway for the decarbonization of steelmaking processes.

THE CHOICE OF COMPONENTS AND THE IMPACT OF SURFACTANTS AND CO-SURFACTANTS ON EPLERENONE NANOEMULSION SYNTHESIS FOR GEL-BASED TRANSDERMAL APPLICATION

Objective: This research aims to establish an efficient methodology for selecting nanoemulsion components to synthesize eplerenone nanoemulsion for gel-based transdermal applications. Methods: The chemical compatibility study of eplerenone was investigated by FTIR, DSC, and solubility in oils, surfactants, and co-surfactants as the criteria for choice. We used visual appraisal and grading to assess the effectiveness of emulsification. Various excipients were tested depending on solubility. The final appearance, dispersibility, and ease of emulsification were used to visually assess the degree of self-emulsification of oil and emulsifier in a 1:3 mass ratio. Co-surfactants were assessed by mixing particular emulsifiers in a 2:1 (w/w) ratio with co-surfactants, and the oily component was added at a 1:3 (w/w) ratio to evaluate Smix's emulsification potential. A central composite design synthesized, evaluated, and optimized eplerenone nanoemulsions. Optimized nanoemulsions were characterized after a thermodynamic stability study for droplet size, ζ potential, viscosity, refractive index, pH measurements, and TEM. All the selected formulations were found to be stable, and the droplet size was found to be&lt;110 nm. Results: Eplerenone was chemically compatible, and its maximum solubility was 171.3±0.92 and 169.3±2.22 in Kollicream®OA and Paceol, respectively. The evidence impressively found that Tween 20 and Kolliphor®EL were discovered as active emulsifiers, and Transcutol®P was revealed to be a co-surfactant. Outcomes showed that the emulsification efficacy of Kolliphor®EL (3% w/w) was able to emulsify Kollicream®OA (1% w/w), and Paceol failed. As well, Smix [Kolliphor®EL (2% w/w) and Transcutol®P (1% w/w)] were able to emulsify Kollicream®OA (1% w/w). Conclusion: The main conclusion from this work is the application of a visual appraisal and grading system to assess the final appearance, dispersibility, and ease of emulsification to eradicate the toxicity and irritation that nanoemulsions can cause. Optimised nanoemulsions can further formulate eplerenone's nanoemulsion gel for transdermal application.

Chitosan impregnated sugarcane bagasse biochar for removal of anionic dyes from wastewater

Wastewater treatment is of utmost importance in providing all equitable and safe drinking water. In the present study, a chitosan impregnated sugarcane bagasse biochar SCNC biocomposite has been synthesized for the removal of Congo red (CR) dye from an aqueous solution. The SCNC biocomposite was thoroughly characterized through Brunauer, Emmett and Teller (BET) and N2 adsorption isotherm, point of zero charge (pHPZC), elemental analysis, Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and Thermogravimetric analysis (TGA) analysis. Moreover, SCNC biocomposite was further employed to remove CR dye from the aqueous solution in batch mode. The SCNC biocomposite could remove more than 95.0% of CR at an initial concentration of (100mgL− 1), adsorbent dosage (0.05 g), time (200 min), pH ~ 3. The SCNC biocomposite achieved maximum adsorption capacity of 170mgg− 1. The equilibrium adsorption data for CR dye were best fitted to the Langmuir isotherm model with R2, 0.999. The kinetic and isotherm were statistically investigated using the chi-square statistic (χ2 ), mean square error (MSE), and the sum of squares error (SSE) Because of the higher correlation coefficient (R2 ≥ 0.999) and lower error functions, the equilibrium CR adsorption isotherms for a single-dye system fit Langmuir and the PSO kinetic model. The thermodynamic studies revealed the spontaneous and endothermic nature of adsorption of CR dye onto SCNC biocomposite. The SCNC biocomposite can be regenerated up to the 5th cycle successfully. The mechanism of CR adsorption onto SCNC was elucidated.

Utilization of poly(methacrylic acid)‐rice straw graft copolymers for Pb2+ ions removal from wastewater: Synthesis, characterization, and adsorption studies

AbstractRice straw bio waste was converted into a high‐performance adsorbent for Pb2+ ions removal by grafting it with methacrylic acid using microwave irradiation. For this purpose, six levels of poly(MAA)‐rice straw graft copolymers having different graft yields % with increasing order and designated as (PMAARSGC‐I to PMAARSGC‐VI) were prepared and characterized using FTIR, SEM, XRD, TGA, zeta potential and BET analysis. Different factors affecting the Pb2+ removal expressed as adsorption capacity such as pH, extent of grafting, treatment time, and lead ions concentrations were studied in detail. Various kinetics models (pseudo‐first‐order, pseudo‐second‐order, Elovich, and intraparticle diffusion), isothermal (Langmuir, Freundlich, Temkin, and Dubinin–Radushkevich) and thermodynamic studies have been applied. The results demonstrated that (a) FT‐IR, SEM, XRD, TGA, zeta potential, and BET analysis confirmed the formation of carboxyl groups onto the graft copolymer, (b) the adsorption capacity increased with increasing the Pb2+ concentration and extent of grafting within the range studied; pH from 1 to 6; and the adsorption time up to 60 min then leveled off afterward, (c) maximum adsorption capacity of poly(MAA)‐rice straw graft copolymer was found to be 118 mg/g at pH 6, 200 mg/L lead ions concentration, adsorption time, 60 min, and 0.1 g adsorbent, (d) the kinetic and isothermal studies revealed that the privilege of Elovich model and pseudo‐second‐order rate equation as well the Langmuir model with more R2 value. The calculated thermodynamic parameters indicated that the adsorption process was achievable, spontaneous, and exothermic at 298–318 K. Finally, the preliminary adsorption mechanism representing the interaction between the adsorbent and adsorbate has been projected.

Ultrastrong coupling limit to quantum mean force Gibbs state for anharmonic environment.

The equilibrium state of a quantum system can deviate from the Gibbs state if the system-environment (SE) coupling is not weak. An analytical expression for this mean force Gibbs state (MFGS) is known in the ultrastrong coupling (USC) regime for the Caldeira-Leggett (CL) model that assumes a harmonic environment. Here, we derive analytical expressions for the MFGS in the USC regime for more general SEmodels. For all the generalized models considered here, we find the USC state to be diagonal in the basis set by the SEinteraction, just like in the CL case. While for the generic model considered, the corresponding USC-MFGS is found to alter from the CL result, we do identify a class of models more general than the CL model for which the CL-USC result remains unchanged. We also provide numerical verification for our results. These results provide key tools for the study of strong coupling quantum thermodynamics and several quantum chemistry and biology problems under more realistic SEmodels, going beyond the CL model.

Mass transfer process in the adsorption of Cibacron Blue (CB) on untreated pea pods (UPPs): kinetic and thermodynamic studies

ABSTRACT In recent decades, there has been extensive use of synthetic dyes in the dye-based industries, particularly the textile sector. Therefore, the aim of this study was to evaluate the adsorption of Cibacron Blue (CB) onto untreated pea pods (UPPs) in a batch system. The effects of the initial CB concentration (10–20 mg/L), solution pH (2–12), adsorbent dose (0–4 g/L), particle size (50–500 μm), and temperature (295–318 K) on the CB adsorption were investigated in batch configuration to determine the optimum conditions. Analyses of UPPs were characterized by Fourier Transform Infrared (FTIR) spectroscopy, Brunauer–Emmett–Teller (BET), and point-of-zero charge (pHpzc = 5.6). Under optimized conditions (pH: 2.5, particle size: 50 μm, time: 40 min, adsorbent dose: 2.5 g/L, and agitation speed: 250 rpm), up to 30.30 mg/g at 25 °C is removed from the solution. The adsorptions kinetics obey rather a pseudo-second-order kinetic model with a determination coefficient of R2 = 0.999. The adsorption isotherms have been used for the determination of thermodynamic parameters, i.e. the negative free energy ΔG° (−4.33 to 0.783 kJ/mol), negative enthalpy change ΔH° (−54.63 kJ/mol), and entropy (ΔS° = −0.1705 kJ/mol.K) indicate that the CB adsorption onto UPPs is spontaneous and exothermic in nature.

Fabrication and adsorption characteristics of cuprammonium cellulose-based membranes for removing anionic and cationic dyes

A cotton linter-based source was used to form conjugate electrospun membranes composed of cuprammonium cellulose, polyethylene oxide, and polyacrylonitrile for the removal of the anionic and cationic dyes from aqueous media. The highest removal efficiencies of 94 %, 89.9 %, 87.4 % were achieved for the anionic dyes Congo red (CR), Metanil yellow (MY), and Methyl orange (MO), respectively, and less so on the cationic dyes Crystal violet (CV), and Rhodamine B (RB) were 55.8 % and 15.1 %, respectively. The pseudo-second-order model effectively described the adsorption kinetics for both types of dyes. The composite membrane exhibited adsorption behaviors following the Dubinin-Radushkevich (D-R) isothermal model. Thermodynamics study suggests that the adsorption process was spontaneous except for the RB dye. The activation energy values of CR, MY, MO, CV, and RB dyes were 27.65, 21.17, 11.50, 10.47, and 71.12 kJ/mol, respectively, confirming the physisorption phenomenon for CR, MY, MO, and CV dyes, while chemisorption occurs for RB dyes. This study investigates the potential of a conjugate electrospun membranes as a reusable adsorbent for dye removal. The effects of solution pH, temperature, and dye concentration on adsorption performance were systematically evaluated. The conjugate electrospun membrane efficiency declined by only 10 % after undergoing five adsorption/desorption cycles.

Green synthesis of biodiesel from magnetic basic biochar derived from Amazonian murici residual biomass: Optimization, kinetic, thermodynamic, and environmental studies

There is a growing need for sustainable catalysts in biodiesel production, however, efficient and low-cost alternatives derived from agro-industrial residues remain limited. This study addresses this gap by exploring murici biochar as a potential source for catalytic development. A basic magnetic catalyst, based on biochar from an Amazonian agro-industrial residue and consisting of sodium impregnated in murici biochar with cobalt ferrite as the magnetic phase, was produced for application in the transesterification reaction of soybean oil. The catalyst was synthesized by wet impregnation with different sodium concentrations to determine the optimal concentration of active phase in the synthesis process. The catalyst demonstrated the best performance and was characterized by TGA, XRD, FT-IR, SEM, EDS, and VSM. A central face-centered composite design was used in the development of a mathematical model for the prediction of ester content. The biodiesel obtained in the optimized reaction conditions of temperature of 90 °C, reaction time of 1.4h, methanol:oil (MeOH:oil) molar ratio of 17:1, and catalyst concentration of 7% obtained ester content of 97.11% and presented physicochemical properties according to the limits established in the ASTM D6751. Moreover, the kinetic and thermodynamic studies revealed that the process follows the pseudo-first order. It also presents an endothermic and not spontaneous character. The green reaction parameters indicate that the reaction using the catalyst is sustainable with low waste generation. Thus, this study show the feasibility of applying the agro-industrial residue in the synthesis of environmentally friendly and low-cost magnetic basic catalysts for the production of biodiesel.

Quantitative and acoustic characteristics of ternary mixes including EDTAs: A thermodynamic study

Quantitative and acoustic characteristics of ternary mixes including EDTAs: A thermodynamic study