Pseudo-second Order Model Research Articles

Bio-sorption of methylene blue using Datura stramonium leaves as adsorbent

Present study was accomplished to prospect the viability of using the Datura stramonium leaves powder (DS) as an adsorbent to remove the methylene blue from aqueous solution. The physico-chemical characteristics of the studied adsorbent were examined. The optimum parameters such as contact time, particle size, absorbent dose, initial methylene blue concentration, and pH were investigated by performing batch experiments models. The kinetics and the isotherms adsorption were evaluated by varying the initial concentration and using the optimum parameters. The optimum of contact time is 30min, with a removal capacity of 89.60 %. The optimal adsorbent concentration to reach the maximum removal of methylene blue (89.54 %) is 18 g/L. An initial methylene blue concentration of 50 ppm is ideal to reach the maximum capacity of removal (92.72 %). The optimum particle size is 80 mm. The kinetics of the adsorption process are in accordance with the pseudo-second order model. Experimental values of the adsorption capacity are close proximity to the optimum values predicted by the pseudo-second order model. Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Harkin-Jura and Hasley isotherms were applied to represent the data obtained from the adsorption studies. The highest R2 values were related to Freundlich, Dubinin-Radushkevich and Hasley isotherm models.

Congo red Removal using Microwave assisted Pyrolysis derived Magnetic Hemp hurd Biochar

Industrial hemp hurd (HH) are the residue obtained after the decortication of the hemp plant for fibre production, which is seldom explored for biochar potential and as adsorbent for dye removal. The present study focused on the microwave-assisted pyrolysis (MAP) of HH for biochar production, magnetization and application for Congo red (CR) removal from aqueous solutions. Magnetic hemp hurd biochar (MHB) depicted a heterogeneous surface with 4.84µm pore size, 17.64 m2/g surface area, and 10.05wt. % Fe. CR removal of 92% was achieved under optimum conditions i.e., treatment time: 120min, pH: 8, and initial CR concentration: 10mg/L with MHB dosage of 0.6g/L. The CR adsorption on MHB was well-fitted with the Freundlich isotherm (R2 - 0.971), owing to the heterogeneous surface of MHB. A strong match with pseudo-second order model (R2 - 0.973), indicated chemisorption as the likely adsorption mechanism. MHB exhibited 87% CR removal efficiency after three successive reutilization cycles. The outcomes of CR removal efficiency and MHB reusability indicated its potential application for adsorptive removal of CR from aqueous systems.

Oxidative pyrolysis for enhanced-CO2 adsorption capacity in biosolid-derived biochar

The study conducts the adsorption kinetic analysis of biosolid-derived biochar produced from pyrolysis and oxidative pyrolysis. The adsorption kinetic analysis is performed at three different temperatures. The characteristics of the adsorption and diffusion mechanisms are evaluated by applying adsorption kinetic models and diffusion mechanism models. The pseudo-first-order model (PFO) and the pseudo-second-order model (PSO) reveal that the CO2 adsorption process of the biosolid can be categorised as physisorption with activation energy below 40 kJ/mol. The CO2 adsorption capacities of the biochar produced at 700°C, 800°C, and 900°C are 6.3, 7.9, and 6.4 mg/g at 45°C, respectively. In contrast, the biochar produced from oxidative pyrolysis shows a CO2 adsorption capacity of 7.5 mg/g at 45°C. Film and intraparticle diffusions are primary rate-limiting factors of the adsorption process. The biochar samples maintain 84-85% of their adsorption capacities after five cyclic tests. The present study demonstrates the CO2 adsorption capacity of biosolid-derived biochar produced from different conditions of pyrolysis, providing an energy-efficient and sustainable solution to CO2 adsorption with solid adsorbents.

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.

A Facile Synthesis of RGO-Ag2MoO4 Nanocomposites for Efficient Lead Removal from Aqueous Solution.

Efficiently treating wastewater, particularly the elimination of heavy metal ions from water systems, continues to be one of the most pressing and complex challenges in modern environmental management. In this work, reduced graphene oxide coupled silver molybdate binary nanocomposites (RGO-Ag2MoO4 NCs) have been prepared via hydrothermal method. The crystalline nature and surface properties of the developed RGO-Ag2MoO4 NCs were proved by XRD, FTIR, SEM, and EDS techniques. Adsorption experiments demonstrated that the nanocomposites (NCs) effectively removed Pb(II) ions within 120 min, achieving a maximum removal efficiency ranging from 94.96% to 86.37% for Pb(II) concentrations between 20 and 100 mg/L at pH 6. Kinetic studies showed that the adsorption process followed a pseudo-second order model. Isotherm analysis presented that the Langmuir model provided the greatest fit for the equilibrium data, with a monolayer adsorption capacity of 128.94 mg/g. Thermodynamic analysis revealed that the adsorption process was spontaneous and endothermic. The results of this study highlight RGO-Ag2MoO4 NCs as a highly promising and eco-friendly material for the effective elimination of Pb(II) ions from wastewater. Their strong adsorption capacity, coupled with sustainable properties, makes them an efficient solution for addressing lead contamination, offering significant potential for practical applications in water treatment systems.

Optimization, Kinetic and Thermodynamic Study of Rhodamine B Removal by Zinc Chloride-activated Arachis hypogaea (Groundnut Husk) biochar

Adsorption of dye from industrial effluent before discharge into the environment has become a major challenge to the food, pharmaceutical, textile, photographic and cosmetic industries. This has led scientists to the search for suitable green solutions. Carbonized and zinc chloride activated Arachis hypogaea (groundnut husk) in a 1:1 ratio was used as an adsorbent for the removal of Rhodamine B from aqueous solution. The adsorbent was characterized by ash content, bulk density, moisture content, pH, Iodine number, surface area and functional group analyses. Key parameters such as initial pH, initial concentration of Rhodamine B dye, temperature and contact time were investigated. The equilibrium data obtained were correlated with Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherms. It was found that both the Freundlich and Langmuir isotherms fit well to the data. The Langmuir isotherm model best describes the uptake of Rhodamine B onto zinc chloride activated groundnut husk biochar with R2 > 0.997. Maximum Rhodamine B. dye removal was observed at a pH of 11.0, with an adsorbent dosage of 1.0 g, a contact time of 125 min, an initial dye concentration of 20 mg/L and a temperature at 315 K. The efficiency of zinc chloride activated groundnut husk biochar for Rhodamine B removal was 99.55% for dilute solutions at 50 g/L. The Fourier Transform Infrared (FTIR) spectra recorded before and after activation showed the numbers of functional groups available for Rhodamine B. molecules to bind onto in the studied adsorbent. The kinetic data were best described by the pseudo-first-order and pseudo second-order models, while the thermodynamic studies indicated a spontaneous and endothermic nature in the adsorption of Rhodamine B by the zinc chloride modified groundnut husk. This research clearly details an innovative approach to utilizing carbonized and zinc chloride-activated Arachis hypogaea (groundnut husk) as an eco-friendly adsorbent for the removal of Rhodamine B from industrial effluents.

Ag2O/ZnO/CuO and Ag2O/ZnO/NiO immobilised on reduced graphene oxide: synthesis, characteristics and its adsorption, catalytic behaviour and antibacterial activities

ABSTRACT Ag2O/ZnO/CuO (A/Z/C) and Ag2O/ZnO/NiO (A/Z/N) nanometal oxides were synthesised in different rations by co-precipitation method and were immobilised on reduced graphene oxide (rGO). The prepared nanocomposites were characterised by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). Their application in the adsorption of MB, RhB and MO dyes, olefin oxidation and antibacterial properties were investigated. The results showed that A/Z/N/rGO adsorbent has 99% (10 min), 93% (20 min) and 97% (12 min) adsorption of MB, RhB and MO, respectively. From the investigation of Freundlich and Langmuir models, it was found that the adsorbent follows Langmuir. Moreover, the reaction thermodynamics was also studied, the reaction was endothermic and spontaneous. The kinetics of dye adsorption MB, RhB and MO on the surface follow a pseudo-second order model. At optimum condition, the conversion and selectivity of α-methylstyrene to acetophenone was >99% by A/Z/N and A/Z/C catalysts. A/Z/C/rGO nanocomposite has good antibacterial properties against two bacteria E. coli and S. aureus.

Innovative Use of Spirogyra sp. Biomass for the Sustainable Adsorption of Aflatoxin B1 and Ochratoxin A in Aqueous Solutions.

This research investigates the efficacy of Spirogyra sp. biomass as an effective adsorbent for the removal of AFB1 and OTA from aqueous solutions. Several factors, including contact time, adsorbent dosage, pH level, and initial mycotoxin concentration, were analyzed to evaluate their impact on adsorption efficacy. The optimal contact time for equilibrium was determined at 60 min, during which the TPA obtained a 91% reduction in AFB1 and 68% removal of OTA. Although increasing the adsorbent dosage improved effectiveness, excessive quantities led to particle aggregation, hence diminishing adsorption performance. The optimal dosage of 5.0 mg/mL optimized the efficacy and use of resources. Adsorption was more efficacious at acidic to neutral pH levels (5-6), enhancing the accessibility of functional groups on the biomass. Kinetic analysis indicated that adsorption process followed a pseudo second-order model, whereas isotherm studies demonstrated a heterogeneous adsorption mechanism, with the Freundlich model providing the optimal fit. The TPB exhibited enhanced adsorption capacities for both mycotoxins, offering a viable solution for mitigating mycotoxin contamination in food and feed. These findings illustrate the significance of biomass treatment techniques in improving mycotoxin removal efficacy and suggest the potential of algal biomass in food safety applications.

Adsorption Studies of Ternary Metal Ions (Cs+, Sr2+, and Co2+) from Water Using Zeolite@Magnetic Nanoparticles (Z@Fe3O4 NPs)

The mixture of three metal ions (Cs+, Sr2+, and Co2+) is commonly found in radioactive waste, which induces several negative health effects. The removal of multiple metal ions is a true challenge for researchers due to the competitive adsorption of ions onto adsorbents. In this study, three metal ions, namely Cs+, Sr2+, and Co2+, have been successfully removed simultaneously from water using zeolite@magnetic nanoparticles (Z@Fe3O4 NPs). The optimized condition for the adsorption of ternary metal ions was obtained at an adsorbent weight of 0.2, pH of 6.0~7.0, and contact time of 60 min. The adsorption mechanism of ternary metal ions onto the surface of Z@Fe3O4 NPs was studied using the Pseudo-first-order, Pseudo-second-order, Elovich, and Intra-particle diffusion models. The Dubinin–Radushkevich Temkin, Freundlich, and Langmuir isotherm models were used to study the isotherm adsorption. The ternary metal ion adsorption (Cs+, Sr2+, and Co2+) on Z@Fe3O4 NPs was followed by the Pseudo-second-order model (PSO) with correlation coefficient (R2) range of 0.9826–0.9997. Meanwhile, the adsorption isotherms of ternary metal ions on Z@Fe3O4 NPs were in line with the Langmuir model with R2 values higher than 0.9206, suggesting monolayer chemisorption with maximum adsorption capacities of 48.31, 15.02, and 10.41 mg/g for Cs+, Sr2+, and Co2+, respectively. Thus, the selectivity trend in the ternary metal ions system towards the Z@Fe3O4 NPs is observed to be Cs+ > Sr2+ > Co2+, which indicates that the competitive effect of Cs+ is the strongest compared to Sr2+ and Co2+ions.

Cnicus Benedictus roots as a low-cost adsorbent for methylene blue dye removal from aqueous solution: kinetic and equilibrium studies

In this research, Cnicus Benedictus roots powder (CBRP) was utilized as a low-cost adsorbent for removing methylene blue (MB) as a cationic dye from aqueous solution. Characterization of CBRP by Boehm titration method, Fourier transform infrared (FT-IR) and environmental scanning electron microscope (ESEM) indicates the presence of different types of functional groups and a very rough surface filled with cavities, suitable for MB adsorption. The effect of various parameters such as CBRP dose (0.2–2 g/1L), contact time (0–180 min), initial pH (1–10), coexisting anions/cations and the initial MB concentration (100–500 mg L−1) on MB adsorption were examined, the results showed that MB uptake depends on the pH of solution, the electrostatic attraction forces, the formation of H-bonds and π–π interactions are the possible CBRP–MB interaction mechanisms. Adsorption kinetic of MB on CBRP was best represented by linear and non-linear form of the pseudo-second order model. The experimental equilibrium data were best described by linear and non-linear forms of Langmuir and Redlich–Peterson isotherm models (R 2> 0.98) with a maximum MB adsorption capacity of 85.47 mg g−1 at 25 °C, the adsorption efficiency R (%) was greater than 90 (%). MB adsorption-desorption experiments showed the reusability of CBRP for five consecutive cycles. According to the obtained results, CBRP can be used as a natural adsorbent material for cationic dyes removal from aqueous solution.

“Chacco” clay from the Peruvian highlands as a potential adsorbent of heavy metals in water

This research aimed to remove Cd (II), Cr (VI), Ni (II), Pb (II), and V (V) from aqueous solutions prepared in distilled water using “Chacco” clay from the Peruvian highlands as adsorbent. The adsorption process was carried out in Batch type systems for 120 min using solutions of each metal at a concentration of 5 mg/L in aqueous systems of a single metal or monometallic (MAS) and solutions of the five metals simultaneously or multimetallic (MMAS). For this purpose, the “Chacco” clay was first characterized by SEM-EDS analysis, finding a laminated clay structure with an elemental composition of C, Al, Fe, Na, Mg, Ca, K, As, Cu, Pd, O, and Ta. The results using 10 g/L of “Chacco” clay showed that the best adsorption efficiency in both MAS and MMAS aqueous systems is achieved at pH = 4 achieving in MAS aqueous systems the removal of 64.16 ± 0.98 % of Cd (II), 95.70 ± 0.81 % of Cr (VI), 97.20 ± 0.89 % of Ni (II), 92. 78 ± 0.79 % of Pb (II), and 95.80 ± 0.67 % of V (V), on the other hand, in aqueous MMAS systems a decrease in adsorption efficiency was observed, managing to remove 6.88 ± 0.53 % of Cd (II), 63.04 ± 0.94 of Cr (VI), 7.81 ± 0.43 % of Ni (II), 62.34 ± 0.77 % Pb (II), and 14.33 ± 0.56 % of V (V). The kinetic study showed that the adsorption mechanism would correspond to chemisorption since the process fitted best to the pseudo-second order model and Elovich. SEM-EDS analysis after adsorption confirmed the presence of the heavy metals under study in the “Chacco” clay. Metal adsorption is evidenced at 1418 cm−1 by -CH2-metal deformation vibrations according to FTIR analysis. In conclusion, the “Chacco” clay would be a promising adsorbent of heavy metals in polluted waters so that scaling up to real environments could be feasible. On the other hand, the “Chacco” clay is consumed by the population of Puno, Peru, therefore its potential impact on health should be evaluated due to its capacity to accumulate metals and the presence of Al in this clay.

Selective extraction of lead from chelator-rich effluents using a biomass-based sorbent

The efficient removal of lead (Pb) from waste streams containing chelators presents a significant challenge due to the high stability and mobility of Pb-chelator complexes. This study investigates a novel approach utilizing a biomass-based sorbent, proline-incorporated dithiocarbamate-modified cellulose with epoxy-cross-linkage (DMC-Pro-Epo6), to extract Pb from effluents with excess chelators. DMC-Pro-Epo6 exhibited exceptional Pb(II) sorption performance under controlled and various chelator-rich conditions. The sorbent maintained high sorption efficiency even with 100-fold excess chelator concentration and competing metal ions. DMC-Pro-Epo6 also outperformed commercially-available ion-selective sorbents in terms of separation efficiency. The sorption kinetics followed a pseudo-second order model, demonstrating rapid sorption with equilibrium reached within 20 min. The maximum sorption capacities of DMC-Pro-Epo6 obtained from the Langmuir isotherm model were 1267 and 659 µmol g−1 in Pb(II)-containing aqueous solution and Pb(II)-containing EDTA solution, respectively. X-ray photoelectron and absorption spectroscopy analyses, along with sorption parameters, confirmed a chemisorption mechanism for Pb(II) sorption onto DMC-Pro-Epo6. Validation of the protocol using real waste samples with complex chelator and base metal ion matrices resulted in a quantitative and selective extraction of 92 to 99 % of Pb(II). This success suggests the potential for scaling up the developed process. Compared to conventional treatment methods, the proposed technique offers a more efficient and streamlined process for separating metal ions and chelators from effluents.

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.

Removal of cefuroxime from aqueous solution by biochars derived from antibiotic mycelial residue.

In China, antibiotic mycelial residue is categorized as hazardous waste. To achieve the harmless and resourceful disposal of cephalosporin, three types of biochars from cephalosporin mycelia residues, namely non-activated carbon (BC1), ZnCl2-activated carbon (BC2), and KOH-activated carbon (BC3), were respectively fabricated by high-temperature pyrolysis carbonization technology. These three kinds of biochars were characterized via iodine value, FTIR, and SEM, and the adsorption performance of the prepared biochars was investigated using cefuroxime (CXM) as the adsorption target. The results indicated that BC3 biochar possesses the most well-developed pores and the highest iodine value of 1367.41 mg/g; The most suitable dosage is 1.6 g/L, and the lower the pH, the more favorable the adsorption effect. The investigation of adsorption kinetics revealed that it conformed to the kinetic model of pseudo-second order, as well as the process of adsorption was governed by the chemical adsorption mechanism, the rate of adsorption was affected by the collective impact of the quantity of active sites present and the interaction strength between the CXM molecules and the biochar. The exploration of adsorption thermodynamics revealed that it aligned with the Langmuir model, the surface of biochar was relatively uniform, and the adsorption was mainly of low coverage; The calculation of thermodynamic parameters demonstrated that the adsorption was exothermic and spontaneous.

Improving the adsorption properties of low surface area hardwood biochar for the removal of Fe+ and PO₄3- from aqueous solution.

Biochar produced from wood residues may provide a new method and material for managing the environment, particularly in terms of carbon sequestration and contaminant remediation. Additionally, biochar produced from wood residues is free of chemical fertilizers, likewise in rice straw, wheat straw, corn straw, etc. This study investigated the removal of iron from aqueous solutions by a novel low-cost and eco-friendly biochar made from hardwood trees and modified by adding MgCl2 for effective phosphate removal. Optimal adsorption conditions were determined through studies of adsorption time, pH, and adsorbent dosage. Batch equilibrium isotherm and kinetic experiments and pre/post-adsorption characterizations using FESEM-EDS, XRD, and FTIR suggested that the presence of carboxyl group elements and colloidal and nano-sized MgO (periclase) particles on the biochar surface were the main adsorption sites for aqueous iron and phosphate respectively. In this study, the HW and MgO-HW biochar showed excellent Dubinin-Radushkevich isotherm (D-R) maximum adsorption capacities of 289.45 and 828.82mg/g for iron and phosphate. The kinetic study for iron and phosphate adsorption was described well by pseudo second-order model and pseudo second-order model respectively. The HW biochar and the prepared MgO-HW biochar exhibited commendable iron adsorption (98.25%) performance at 10 pH units and phosphate (96.22%) at pH 6 respectively. Thus, this research reveals a waste-to-wealth strategy by converting hardwood waste into mineral-biomass biochar with excellent Fe and P adsorption capabilities and environmental adaptability.

Sodium alginate-g-polyacrylamide hydrogel for water retention and plant growth promotion in water-deficient soils

Natural polymer-based hydrogels are preferred as soil water retention agents due to their inherent biocompatibility and biodegradability. Generally, these natural polymers are chemically modified by graft polymerization of vinyl monomers to improve their water absorption and retention properties. Among the polysaccharides used to prepare natural hydrogels, those based on sodium alginate (Alg) stand out for their high-water absorption and retention capacity, as well as for their ability to promote plant growth. The main objective of this study was to develop a biodegradable alginate-based hydrogel as a water retainer to promote plant growth under water deficit conditions. The synthesis was achieved by grafting poly(acrylamide) (PAM) onto Alg backbone, using bisacrylamide as chemical crosslinker and different ratios of alginate:acrylamide (Ac). In addition, Eucalyptus nitens seedlings were used as a model plant to evaluate the effect of alginate-g-polyacrylamide (Alg:PAM) hydrogel application to the growing medium on plant survival, growth, and physiological responses under both well-watered and water-deficient soil conditions. The maximum degree of swelling (65 g/g) was obtained for the hydrogel prepared. The pseudo-second order model described the water uptake kinetics of the hydrogel. The degradability of Alg:PAM hydrogel reached up to 85 % in 5 weeks in soil and occurs by breaking the glycosidic bonds of the alginate. The E. nitens seedlings cultivated with different doses of Alg:PAM hydrogel (4:1 Alg:Ac) showed higher values of height and root diameter relative growth, survival and photosynthetic responses in comparison to non-treated plants. The results indicate that Alg:PAM hydrogel (4:1 Alg:Ac) has promising applications in forestry as a water retention and seedling growth promoter under water deficient conditions.

Adsorptive potential of apricot (Prunus Armeniaca) stone in the removal of Cr (VI) and Fe (II) ions from Aquatic Systems: Kinetic and isothermal investigations

Biogenic adsorbents have emerged as a promising alternative to the traditional remediation techniques of heavy-metals contaminated water treatment. Using apricot (Prunus Armeniaca) stone as a naturally derived adsorbent, the current study provides a comprehensive analysis of the kinetic and isothermal characteristics associated with Cr (VI) and Fe (II) ion adsorption. The results show that 0.5 mg of the adsorbent removed approximately 90 % of Cr (VI) and Fe (II) ions from 100 ppm solutions within 120 min at 298 K at 300 rpm stirring speed. Equilibrium was attained within 90 to 120 min, with a significant increase in the removal percentage observed in the first 30–40 min for both metals compared to the subsequent 80–90 min. The optimal pH conditions for adsorption were determined to be acidic (pH = 1.5) for Cr (VI) and neutral (pH = 7) for Fe (II). The adsorption kinetics followed a pseudo-second order model, while the isothermal equilibrium data best fit the Freundlich model over the Langmuir model. Moreover, the thermodynamic parameters, including ΔG°, ΔH°, and ΔS°, indicated that the sorption process is spontaneous, feasible, and endothermic. The response surface methodology (RSM) analysis showed a high level of accuracy in predicting the percent removal. These findings illustrate the effectiveness of apricot stone as a low-cost and environmentally conscious adsorbent, contributing to the development of sustainable water treatment technologies.

Insights into the adsorption mechanism of chlorpyrifos on activated carbon derived from prickly pear seeds waste: An experimental and DFT modeling study

The removal of chlorpyrifos (CPF) from water was achieved using activated carbon (AC) derived from prickly pear seeds (PPS) wastes, developed through chemical activation with phosphoric acid. Several physico-chemical characterization methods were employed. The determination of surface functions using the Boehm assay indicated that the processed AC predominantly possesses acidic functions. The results obtained from the Boehm assay were corroborated by the pH value of the point of zero charge (pHpzc), which was equal to 2.5. Specific area calculation by the BET (Brunauer Emmett Teller) method revealed a large specific area (SBET) of 1077.66 m2 g⁻1. Adsorption experiments of CPF on AC demonstrated that the pseudo-second order (PSO) model and the Freundlich model were the most suitable for kinetic and isothermal modeling, respectively. The maximum CPF adsorption capacity of the PPS AC was found to be approximately 35 mg g⁻1. A theoretical study employing the density functional theory (DFT) was conducted using the B3LYP/6-311G (d, p) method. The most reliable adsorption energy (Eads) and Gibbs free energy (ΔGads) values between CPF and the functional groups on the AC surface were calculated. Results indicated a strong interaction between the lactone group of AC and CPF (ΔGads = −7.15 kcal mol⁻1, ΔEads = −21.55 kcal mol⁻1) and the hydroxyl group (ΔGads = −6.61 kcal mol⁻1, ΔEads = −20.66 kcal mol⁻1). This study demonstrates that activated carbon possesses significant adsorption power, making it highly effective for depolluting water contaminated by pesticides. The application of the theoretical DFT method enhances the understanding of the adsorption phenomenon of CPF on AC.

Aspergillus versicolor mediated biofabrication of zinc phosphate nanosheets for exploring their antimycotic activity and development of alginate-based nanocomposite for enhanced dye degradation

The production of novel, suitable, and cost-effective nanocomposites are highly required for its prospective application in the remediation of environmental pollutants and as antimycotic agents. Zinc phosphate nanosheets (ZP-ns) were fabricated by harnessing the exometabolites of Aspergillus versicolor and then incorporated within an alginate biopolymer (ZP-ns@Alg) to improve the biosorptive removal of the methyl orange (MthO) dye from its aqueous solution. For the very first time, the antimycotic activity of the green synthesized ZP-ns was unveiled. The mycelial growth inhibition was obtained in a dose-dependent manner with significant (P < 0.05) behavior compared to the control plates. The biosorption conditions using ZP-ns@Alg microbeads were optimized using the response surface methodology-based central composite design (RSM-CCD) to maximize the biosorption efficiency. The highest biosorptive efficiency was achieved at pH 4.0, biosorption dosage 0.07 g, contact time 50 min, dye concentration 100 mg/l, and shaking speed 100 rpm. The equilibrium data were more tailored to the pseudo-second order (PS) model with an R2 of 0.9955 and a Langmuir isotherm (R2 = 0.9945) with a maximum biosorptive capacity (qmax) of 166.95 mg/g and an average RL value of 0.0003, indicating favorable biosorption. The removal capacity was reduced to ∼90 % after the 6th cycle, which is a robust signal that the developed biosorbent microbeads could be recycled and regenerated for a prolonged time. These results marked the application of ZP-ns as a novel antimycotic agent with excellent activities. Microbeads, made from low-cost biopolymers, can be applied to remediating environmental pollutants from wastewater.

Influence of pyrolysis time on removal of heavy metals using biochar derived from macroalgal biomass (Oedogonium sp.)

In this study, pyrolysis was performed at different times to convert Oedogonium biomass into biochar. The physicochemical properties show that the pyrolysis time significantly impacts structural and morphological changes in biochar samples. The influence of pyrolysis time on the removal of multiple heavy metals was investigated. Owing to the presence of abundant functional groups, inorganic minerals and porous nature, biochar obtained from a 40 min pyrolysis time showed higher removal efficiency of heavy metals compared to biochars pyrolyzed at 20 mins and 60 mins even with higher concentrations of metal ions. The maximum adsorption capacity was observed 9.33, 10.74, 322.58, 13.70 and 9.11 mg/g with the biochar prepared at the pyrolysis time of 40 mins for Co, Ni, Cu, Zn and Cd, respectively. The adsorption isotherm is well fitted with the Langmuir adsorption model for heavy metals adsorption, and the kinetic study is well-defined by a pseudo second-order model.