Pseudo-second Order Kinetic Model Research Articles

Synthesis of reduced graphene oxide and its application for the removal of anaionic dye TURQUOISE GN

Although graphene oxide (GO) and its derivatives showed excellent adsorption capacities for dyes and heavy metals, its application is limited to cationic and commercially used dyes. In this article reduced graphene oxide (RGO) was prepared and applied for the adsorption of a commercially used anionic dye. GO was prepared from graphite powder by modified Hummer’s method and reduced to RGO by hydrazine hydrate. Characterization of prepared RGO was carried out by Raman spectroscopy, ESEM, XRD, elemental analysis and the surface charge was determined by zeta potential analysis. An anionic dye TURQUOISE GN (TGN) was used to investigate the adsorption capacity of prepared RGO. To know the adsorption properties of RGO, the effects of solution pH, dosage of adsorbent, concentration of the dye, adsorption time and temperature on adsorption capacity of RGO were also studied. The distribution of the adsorbate on the RGO surface was studied with both Langmuir and Freundlich isotherm models and it was found that it preferably followed Langmuir model. The theoretical maximum adsorption capacity was found to be 588.24 mg/g at pH 7. To find out the mechanism of the adsorption of TGN on RGO pseudo-first-order and pseudo-second order kinetic models were applied and the results fitted perfectly with the second-order kinetic model. The exhausted RGO was regenerated by treating with 2 % HCl followed by washing with demineralized water and showed moderate adsorption capacity.

Study on the mechanism of lignin non-productive adsorption on cellobiohydrolase

Enzymatic hydrolysis is important for lignocellulosic biomass conversion into fermentable sugars. However, the nonproductive adsorption of enzyme on lignin was major hinderance for the enzymatic hydrolysis efficiency. In this study, non-productive adsorption mechanism of cellulase component cellobiohydrolase (CBH) onto lignin was specific investigated. Research revealed that the adsorption behavior of CBH on eucalyptus alkali lignin (EuA) was affected by reaction conditions. As study on the adsorption kinetic, it was indicated that the adsorption cellulose binding domain (CBD) of CBH onto EuA well fitted with Langmuir adsorption model and pseudo second-order adsorption kinetics model. And the tyrosine site related to the adsorption of CBD onto lignin was proved by the fluorescence and UV spectra analysis. The results of this work provide a theoretical guidance to understanding the nonproductive adsorption mechanism and building method to reduce the adsorption of cellulase on the lignin.

Adsorptive Sequestration of Methylene Blue Dye from Aqueous Solution Using Novel Roystonea regia fruit Pericarp: Isotherm, Kinetics, and Thermodynamics

The batch adsorptive sequestration of methylene blue from an aqueous solution using unripe Roystonea regia fruit pericarp biomass was investigated in this study. The characteristic nature of the biosorbent was studied using various analytical instruments including Fourier Transform Infra-red spectrophotometer, Scanning Electron Microscope, Energy Dispersive X-ray, X-ray diffractometer, and the Brunauer-Emmett Teller. The adsorption study was perfomed at different experimental conditions including pH, contact time, initial dye concentration, temperature, agitation speed, and biosobent dose. From the results of this study, the optimum biosorption of MB was achieved at 120 min contact time, pH 10, room temperature (298 K), 150 rpm agitation speed and dosage of 100 mg/150 mL dye solution. With 132.30 mgg-1 maximum sorption capacity, the Langmuir isotherm best describes the biosorption equilibrium data. At all initial concentrations, the biosorption kinetics of methylene blue onto the biosorbent fitted best to the pseudo-second order kinetics model, with R2 values ≥ 0.999 and qcal being similar to the qexp. The kinetics study also showed the involvement of intra-particle diffusion in the rate-determining step; although not as the sole limiting step of the sorption process. The results of the thermodynamics study showed the high feasibility, spontaneity, and exothermic nature of the biosorption of methylene blue onto the biosorbent. This study concludes that Roystnea regia fruit pericarp would make an economically viable and renewable biosorbent for practical eco-friendly sequestration of MB dye from wastewaters.

Palm Oil Mill Effluent Biochar as An Alternative Potassium Source: Effect of Pyrolysis Time and Its Kinetic Release

Palm Oil Mill Effluent (POME) is one of the waste products of palm oil processing that can be processed into a biochar. POME biochar contains high levels of nutrient, such as NPK which can be used an alternative potassium source material. This study aims to produced biochar from POME and the influence of pyrolysis time on the characteristics and its kinetic release. Biochar production from POME was conducted at 300oC with pyrolysis time variation of 1 hour, 3 hours and 5 hours. Biochar characterization was conducted using Fourier Transform Infrared (FTIR) Spectroscopy, Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX), Surface Area Analysis (SAA). Study of potassium release was conducted by mixing one gram amount of biochar with 0.01 M CaCl2 as a function of time. The used kinetics modelling in this study are first-order, second-order, pseudo-first order, pseudo-second orde. The results showed that the biochar yield decreased, while the biochar pH value, exchangeable potassium, non-exchangeable potassium and surface area increased with the increasing of pyrolysis time. The pseudo- second order model is the most fitted model to describe the potassium release. The pseudo-second order kinetics model gave K release rates of 0.018; 0.024; 0.020; 0.014 (mg g-1min-1), the qe values are 0.814; 0.839; 0.927; 1.111 (mg g-1), respectively.

Aging and adsorption behavior of PP-MPs for methylene blue and tetracycline in unitary and binary systems

The omnipresence of microplastics (MPs) around the world has attracted extensive attention in the past decade with more focuses on the interactions of standard MPs without additives in regular shapes and individual pollutant, whereas the actual MPs containing various additives in irregular shapes and complex pollutants are often co-occurrence in the environments. In this paper, the adsorption performance of disposable polypropylene (PP) cups-based MPs subjected to ultraviolet irradiation was investigated in unitary and binary water matrices. The surface characteristics were analyzed and the experimental data of adsorption were fitted by various kinetic and isotherm models, and the results indicated that more cracks and oxygen-containing functional groups with decreased hydrophobicity were produced with aging, and electrostatic attraction and hydrogen bonding dominated methylene blue (MB) and tetracycline (TC) capture in the individual system. Moreover, pseudo-second order kinetic model better described the adsorption processes. In the binary system, the co-existence of TC promoted MB uptake, while the presence of MB inhibited TC capture. In addition, TC adsorption was enhanced by Ca2+, maybe due to its complexation effect, while the presence of mono- and divalent inorganic salts inhibited MB capture. This research provides useful insights for the fate of PP-MPs and organic pollutants in the complex environments.

Oily wastewater treatment using low-cost and highly efficient natural and activated Iraqi bentonite

One of the most dangerous organic compounds to the environment is gasoline emulsions, discharged without prior treatment by most oil refining industries. This study focuses on the modification of bentonite clays by acid and thermal activation to maximize their adsorption capacity for treating refinery wastewater. The surface properties and porous structure of the adsorbents were investigated with the use of BET, SEM, FTIR, XRD, XRF, EDX, and MAP methods. Based on the results of BET analysis, the surface area of the raw bentonite (RB) and activated bentonite (AB) was (17.57, 69.72) m2 /g. The four independent variables, namely the initial gasoline concentration (200–1000 mg/L), solution pH (3−9), contact time (30–120 min), and adsorbent dosage (ranging from 0.05 to 0.15 g/L). According to the results, the maximal adsorption capacity (74.6.38, 138 mg/g) by RB and AB was achieved using the following optimized conditions: initial COD gasoline concentration of 1000 mg/L, pH= 6 for RB and pH= 3 for AB, contact time 120 min, and adsorbent dosage 0.15 g for RB and AB. Additionally, the kinetic and equilibrium studies demonstrated that the present adsorption process's kinetics and equilibrium behavior were adequately represented by the pseudo second-order kinetic model and the Langmuir isotherm. The data by Langmuir isotherm showed that the maximum adsorption capacity for RB and AB was equal to 83 and 140.84 mg/g, respectively. Furthermore, thermodynamic studies demonstrated that the present adsorption procedures were both spontaneous and endothermic. The mechanism of gasoline adsorption onto RB and AB was effectively investigated with the assistance of characterization techniques. The current study demonstrates that RB and AB can be utilized as adsorbents for the elimination of gasoline with high efficiency.

Selective separation of lead (II) from foodstuffs and environmental samples by adsorption onto modified truffle peels with nanoparticles [TPs/TiO2(NP)] as a novel biomass

ABSTRACT This study aims to examined truffle peel powder modified with nanoparticles [TPs/TiO2(NP)] as a solid adsorbent for the removal of lead ions Pb(II) from environmental media and foodstuffs. The characterisation of TPs/TiO2(NP) was studied by a Fourier-transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and energy dispersive X-ray (EDX). Through the application of several adsorption isotherm models, the Langmuir at 25°C revealed to be most appropriate, having the highest R2 (0.961), and the maximum Pb(II) adsorption capacity was found 0.908 mg g−1. In addition, the various kinetics models were applied, and the data was well-fitted by the pseudo-second order kinetics model (R2 = 0.9997). Thermodynamic parameters indicated that the technique of adsorption had been endothermic (∆H = 30.79 J mol−1), The value of ΔG indicates the spontaneous and physical nature (- 29.26 KJ mol−1) and the positive value of ∆S indicates a moderate step of sorption of the Pb(II) complex ion associate (98.32 J). Foodstuffs (energy drinks and ice pops) and environmental samples (tap water) were successfully confirmed with a good recovery.

Biogenic mediated green synthesis of NiO nanoparticles for adsorptive removal of lead from aqueous solution

The spread of heavy metal in water bodies, particularly lead (Pb), has occurred as a global threat to human existence. In this study, NiO nanoparticles (NPs) was prepared by coprecipitation approach using Hagenia abyssinica plant extract mediated as a reducing and template agent for the removal of Pb from aqueous solution. X-ray crystallographic diffraction (XRD), Scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and Brunauer-Emmett-Teller (BET) techniques were employed for the characterization of as prepared NiO NPs. The efficacy of adsorbent was evaluated on the removal of Pb2+ by varying the adsorptive parameters such as pH, Bio-NiO amount, interaction time, and Pb2+ concentration. The adsorption was 99.99% at pH, 0.06 g of NiO NPs dose, 60 mg L−1 concentrations of Pb2+ within 80 min contact time. The higher removal efficiency is could be due to higher surface area (151 m2g-1). The adsorption process was best fitted with Freundlich isotherm and pseudo-second order kinetic models, implying that it was chemical adsorption on the heterogeneous surface. The adsorption intensity (n) was found to be 1/n < 1 (0.47) indicating adsorption of Pb2+ on the surface of Bio-NiO NPs was favorable with a maximum adsorption capacity 60.13 mg g−1. The reusability studies confirmed that the synthesized bio-NiO NPs were an effective adsorbent for removing Pb2+ from aqueous solution up to five cycles.

A novel zirconium glyphosine carbon nanotube composite for fast and ultraeffective In(Ⅲ) capture

Extraction of In(Ⅲ) from the tail liquid of zinc ore which possesses the large amounts of Zn(Ⅱ) and the characteristics of highly acidity, remains a critical challenge. Adsorption method can be considered as an effective and green strategy to recovery In(Ⅲ). However, the adsorption capacity of mostly reported adsorbents is unsatisfactory toward In(Ⅲ) in the acidic environment. In this work, an effective In(Ⅲ) trap is developed by using a mild, simple strategy that introduces zirconium glyphosine coordination networks in situ loaded on carbon nanotube. Benefiting from the characteristics of abundant carboxyl and phosphate groups, excellent hydrophilicity and thermal stability, the resultant zirconium glyphosine carbon nanotube composite (xZrGP-CNT) exhibits remarkable adsorption capacity (193.72 mg g-1) toward In(Ⅲ) under pH 2.5 exceeded most of the reported adsorbents, and its adsorption behavior is consistent with pseudo-second order kinetic and Langmuir isotherm models. In addition, the obtained 2ZrGP-CNT shows prominent kinetics that reaches equilibrium only within 2 h, superior selectivity and excellent regeneration performance for In(Ⅲ) capture, which indicates the highly encouraging potential for the recovery of In(Ⅲ) in practical ore fluids. Our work poses a new way to recovery of In(Ⅲ) under acidic environments with superior adsorption performance and broadens the potential of organocphosphonates for recovering In(Ⅲ).

Lead (Pb) Sorption Kinetics by Clay Minerals: Bentonite and Zeolite

Background: Heavy metal pollution chiefly lead (Pb) causes various environmental disequilibrium and health hazards. Immobilization of lead (Pb) usingclay minerals is cost effective for metal remediation due to their higher surface area and negative charges. Methods: This study was taken up to assess the Pb removal potentials of bentonite and zeolite from contaminated water and to study the effect of sorbent dosage, initial Pb2+ concentrations and incubation time intervals on Pb adsorption and desorption was studied. Result: Zeolite was effective in immobilising Pb (78.0%) than bentonite (70.9%) which increased with increasing sorbent dosage and time intervals. The pseudo second-order kinetic model described the Pb adsorption precisely. Chemisorption was the dominant mechanism operating in aqueous solution system, hence, it could be concluded that zeolite can be utilized as an efficient sorbent for wastewater treatment.

Enhanced uranium removal from leach liquor using raw and activated sludge as sustainable adsorbents

ABSTRACT To eliminate uranium from sulphate leach solution, this study introduces an economical, environmentally friendly adsorbent derived from dewatered municipal sludge (RS) and activated (AS) using calcium oxide. Various analytical methods, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), Brunauer – Emmett – Teller (BET) analysis, and X-ray fluorescence spectroscopy (XRF), were employed in the characterisation of both materials. The efficacy of these adsorbents in removing uranium from sulphate leach fluid was systematically explored resulting in the achievement of a maximum adsorption capacity of 33.0 mg g−1 and 60.2 mg g−1 for RS and AS respectively. These adsorption capacity were detected using the following operational parameters: solution pH equals 2.0, 240 min as a contact time between the adsorbent and U(VI) solution, U(VI) initial concentration of 250 mg L−1, adsorbent dosage of 5.0 g L−1 and room temperature. The pseudo-second order kinetic and Langmuir isotherm models were determined to be the most suitable for the U(VI) adsorption process, showing a chemisorption, monolayer, and uniform process for the uranium adsorption by both materials. Using 1.0 M hydrochloric acid, over 96% of the U(VI) was successfully desorbed from the loaded sorbent, and AS sorbent held its stability for six sorption/desorption cycles in a row. Overall, this study offers a promising solution for sewage sludge disposal while addressing economic and environmental concerns.

Green-synthesized, biochar-supported nZVI from mango kernel residue for aqueous hexavalent chromium removal: Performance, mechanism and regeneration

A biochar-supported green nZVI (G-nZVI@MKB) composite was synthesized using mango kernel waste with “dual identity” as reductant and biomass of biochar. The G-nZVI@MKB with a Fe/C mass ratio of 2.0 (G-nZVI@MKB2) was determined as the most favorable composite for hexavalent chromium (Cr(VI)) removal. Distinct influencing parameters were discussed, and 99.0% of Cr(VI) removal occurred within 360 min under these optimized parameters. Pseudo-second order kinetic model and intra particle diffusion model well depicted Cr(VI) removal process. The XRD, FTIR, SEM and XPS analyses verified the key roles of G-nZVI and functional groups, as well as the primary removal mechanisms involving electrostatic attraction, reduction, and complexation. G-nZVI@MKB2 exhibited a good stability and reusability with only a 16.4% decline in Cr(VI) removal after five cycles. This study offered evidence that mango kernel could be recycled as a beneficial resource to synthesize green nZVI-loaded biochar composite for efficient Cr(VI) elimination from water.

Peptides-modified cellulose microspheres for adsorption of ochratoxin A: Performance and mechanism

In this study, peptides with ochratoxin A (OTA) recognition and adsorption capability were designed, among which lysine, histidine, arginine and tyrosine were crucial. Peptide CYFRFYSNLHPK showed the strongest affinity for OTA (Ka = 1.74 × 105 M−1). Theoretical calculations revealed that the differences in the affinity of peptides for OTA were attributed to differences in the type, number and position of amino acids residues. Peptides were conjugated with porous cellulose microspheres to form peptide-modified pretreatment materials (Pep-MPA-RCMs) for adsorption of OTA. The morphology and composition of the prepared Pep-MPA-RCMs were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, fourier transform infrared spectroscopy, thermogravimetric analysis and X-ray diffraction. The effects of pH, adsorption time, initial concentration and temperature on the adsorption process were investigated. The adsorption performance was correlated with the pseudo-second order kinetic and Sips adsorption isotherm model. Thermodynamic studies further proved that the adsorption was exothermic and the prepared Pep-MPA-RCMs showed the maximum adsorption capacity of 9.87 mg/g for OTA at 25℃. A simple adsorption column for OTA was prepared by using Pep-MPA-RCMs as filler material, which still maintained more than 80 % of the removal rate after five consecutive adsorption-elution cycles. The prepared pretreatment material was successfully applied to remove OTA in real samples and was a promising adsorbent for practical applications.

Comparison of two carbonaceous supported Fe-rich adsorbents for arsenate removal: A functionalisation and mechanistic study with applicability to groundwater treatment

The presence of arsenic in groundwater, and through this in drinking water, has been shown to present a serious risk to public health in many regions of the world. In this study, two iron-rich carbonous adsorbents were compared for the removal of arsenate (As(V)) from groundwater. Biochars (FeO-biochar and FeO-pyrochar) derived from biomass waste were functionalised in two different ways with iron chloride for comparation. Batch and dynamic parameters were optimised to achieve >99% As(V) removal efficiency. Experimental data were best described by the pseudo-second order kinetic model, while multi-stage diffusion appeared to limit mass transfer of As(V). Among the isotherm models evaluated, the Freundlich model best described the experimental results with high correlation coefficients (R2 ≥ 0.94) for both adsorbents. Monolayer adsorption capacities were found to be 4.34 mg/g and 8.66 mg/g for FeO-biochar and FeO-pyrochar, respectively. Batch studies followed by instrumental characterisation of the materials indicated the removal mechanisms involved to be electrostatic interactions (outer-sphere), OH− ligand exchange (inner-sphere complexation) and hydrogen bonding with functional groups. Higher pHpzc (9.1), SBET (167.2 m2/g), and iron/elemental content for the FeO-pyrochar (compared with the FeO-biochar) suggested that both surface chemistry and porosity/surface area were important in adsorption. Dynamic studies showed FeO-pyrochar can be used to remove As(V) from groundwater even at low ‘environmental’ concentrations relevant to legislative limits (<10 μg/L), whereby 7 g of FeO-pyrochar was able to treat 5.4 L groundwater.

Solventless synthesis of bixbyite (Mn2O3) and hausmannite (Mn3O4) nanoparticles for ammonia nitrogen removal

Excessive accumulation of ammonia nitrogen (AN) in water resources poses serious health effects to humans, and control of its discharge in wastewater has been a primary global concern. Therefore, it has to be removed by robust, eco-friendly, and cost-effective approaches. In this study, Mn2O3 and Mn3O4 nanoparticles (NPs) were facilely synthesized by solid-state thermolysis, and characterized by XRD, FTIR, SEM, and TEM techniques. XRD results revealed the formation of single-phase cubic bixbyite, Mn2O3 and, tetragonal hausmannite, Mn3O4 nanoparticles exhibiting crystallite size of 27.69 and 19.38 nm, respectively. Morphological analysis shows the formation of agglomerated nanoparticles with varying shapes. The experimental isotherm results indicated that AN sorption by Mn2O3 could be well described by Freundlich model, indicating multilayer adsorption on heterogeneous surface. Contrarily, AN adsorption by Mn3O4 was consistent with the Langmuir model, representing a monolayer physisorption process on a homogeneous surface. The pseudo-first-order kinetic model fitted well to the experimental data than the pseudo-second order kinetic model. The Langmuir sorption capacities (qm) for Mn2O3 and Mn3O4 were 23.642 mg/g and 52.779 mg/g, respectively. Thermodynamic experimental kinetic data demonstrated that AN adsorption on the two forms of manganese oxides was an exothermic and spontaneous process. Regeneration experiments inferred that both Mn2O3 and Mn3O4 adsorbents could be reused.

Cost-effective synthesis of magnetic graphene oxide nanocomposite from waste battery for the removal of arsenic from aqueous solutions: Adsorption mechanism with DFT calculation

In this study, magnetic graphene oxide (MGO-Fe3O4) nanocomposite was prepared by co-precipitating of FeCl3.6H2O and FeCl2.4H2O on waste battery-derived graphene oxide and used as an adsorbent for the efficient removal of As(III) from aqueous solutions. The prepared nanocomposite was characterized by Fourier transformed infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, zeta potential, and a vibrating sample magnetometer. These characterizations revealed that spare like Fe3O4 nanoparticles (10.5 nm) were decorated on graphene oxide nanosheets and showed excellent saturation magnetization (89.73 emu/g). The adsorption of As(III) by MGO-Fe3O4 was optimized by analyzing various parameters. Experiments showed that 98 % of As(III) was removed at neutral pH in a just 20 min, even though the adsorbent dose was only 0.14 g/L. The adsorption kinetic and isotherm were best fitted with the pseudo-second order kinetic and Frendlich isotherm model. The maximum adsorption capacity (qmax) was found to be 50.2 mg/g at room temperature. Thermodynamic studies showed that the As(III) adsorption process was spontaneous and exothermic in nature. The enhanced adsorption capacity and magnetic properties of MGO-Fe3O4 are crucial in the drinking water treatment process due to the easy magnetic separation of MGO-Fe3O4 from aqueous solution after the adsorption process. Density Functional Theory (DFT) was also used to investigate the interaction between MGO-Fe3O4 and As(III), which further suggested that MGO-Fe3O4 and As(III) mostly interact with each other through surface complexation and hydrogen bonding.

UPTAKE OF Co(II), Pb(II) AND Ni(II) IONS BY Annona senegalensis STEM BARK BIOCHAR FROM AQUEOUS SOLUTION: OPTIMIZATION, KINETIC AND THERMODYNAMIC STUDIES

The concern for heavy metal pollution in the environment is especially so since they are non-biodegradable. The use of agro materials in the removal of these heavy metal pollutants has been recognized as a low-cost alternative to the costly conventional remediation techniques. The equilibrium sorption of the chemically activated Anonna senegalensis stem bark was investigated. Using standard techniques, the physicochemical properties of activated carbon (MAASC) were ascertained. By using a simultaneous batch adsorption approach, the adsorption of Co2+, Pb2+, and Ni2+ onto MAASC was examined as a function of pH, solution temperature, initial metal ion concentration, agitation time, adsorbent dose, particle size, and carbonization temperature. The equilibrium sorption data generated were fitted into Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherm models as well as pseudo first-order, pseudo-second-order and intraparticle diffusion kinetic models. From the obtained results, it was discovered that the Langmuir isotherm provided the best match conformation of all the models, except for Pb2+, which was best for Freundlich with an R2 of 0.95. Physisorption was shown to be the mechanism by Dubinin-Radushkevich. For Co2+, Pb2+, and Ni2+, respectively, the pseudo second-order kinetic model had R2 values of 0.997, 0.999, and 0.999 that best matched the data. Both intraparticle diffusion and the boundary layer effect also contributed to regulating the rates of the adsorption process. The study's thermodynamic results showed that Ho for Co2+, Pb2+, and Ni2+ were 27.51, 19.70, and 13.37 KJ/mol, respectively. These values are all positive and suggest an endothermic reaction, supporting the physisorption mechanism.

Removal of Humic Acid from Water by Adsorption Using Chitosan and Metal Organic Framework ZIF 8 Loaded Chitosan Adsorbents

Water is the most necessary need for life on the earth. There are a lot of organic pollutants in water. One of the organic pollutants is natural organic substances. Humic acid, a natural organic substance, turns into very harmful substances along with other pollutants. In this study, the humic acid removal from aqueous solution by adsorption using chitosan and chitosan/ZIF 8 composite spheres was examined. Chitosan spheres cross-linked with epichlorohydrin (ECH) and composite spheres consisting of metal organic framework ZIF8 and chitosan were prepared as adsorbents. Equilibrium, kinetic, and thermodynamic studies were investigated for humic acid adsorption by pristine chitosan-ECH and composite chitosan/ZIF 8 adsorbents. Chemical adsorption was found to be compatible with the Freundlich isotherm model and the pseudo-first-order kinetic model for pure chitosan adsorbents. Studies were carried out using chitosan/ZIF8 composite adsorbent, and the most suitable models for chemical adsorption were determined as Langmuir isotherm and pseudo-second order kinetic model. The response surface method was applied with the design expert program to determine the optimum experimental conditions. The adsorption tests were carried out using chitosan-ECH, ZIF 8 and chitosan/ZIF 8 adsorbents for specified optimum conditions, and the humic acid removal was determined as 95.1%, 98.3%, and 97.3%, respectively. In addition, desorption was performed using chitosan-ECH and chitosan/ZIF 8 spheres, and the desorption efficiency was found to be 20.9% and 82.5%, respectively. It has been observed that the developed adsorbents have potential in removing humic acid from water.

By-product Eucalyptus leaves valorization in the basic dye adsorption: kinetic equilibrium and thermodynamic study

Abstract Algerian Eucalyptus Leaves (AEL), a natural biodegradable adsorbent abundantly available, was used for the removal of methylene blue (MB) dye. The AEL properties for the removal of MB were investigated under different conditions by varying the AEL amount, MB concentration, pH of the solution and the reaction temperature. Scanning electron microscopy (SEM) and infrared spectroscopy (FTIR) techniques have been used to characterize AEL biosorbent. Experimental results showed that the adsorption of MB dye at the concentration of 50 mg L−1 reached to 91 % at pH 10 with a stirring speed of 200 rpm and after 180 min of reaction time. The experimental data were analyzed using the linear forms of different kinetic models (pseudo-first order kinetic model, pseudo-second order kinetic model, and intra-particle diffusion models). The results demonstrated that the adsorption kinetics of MB was consistent with the pseudo-second order model with R 2 value of 0.9969. The isotherm models Langmuir, Freundlich, Dubinin, Elovich, Brunaut Emmet Teller and Temkin models were also investigated to describe the adsorption equilibrium. The results show that the AEL adsorption is in accordance with Temkin isotherm. The thermodynamic study revealed that the adsorption is spontaneous and exothermic. Therefore, as a cheap green adsorbent with high MB adsorption performance, AEL is expected to become one of the best candidate materials for future industrial wastewater treatment.

Investigating the sorption behavior of selenite on commercial partially oxidized magnetite nanopowder under aerobic conditions: Characterization and mechanisms

Selenium, which belongs to essential elements, has a narrow margin between necessity and toxicity. Anthropogenic activities may lead to its elevated concentrations in aquatic ecosystems, particularly in the undesirable form of toxic selenite, due to its high environmental mobility. Hence, it is imperative to devise effective technologies to limit its potential migration through the environment. Therefore, the development and evaluation of new adsorbents for its effective removal from selenium-contaminated waters are crucial for both human health and environmental stability in affected areas. Specifically, magnetite-based nanomaterials showed promise as sorbents due to their capacity to immobile contaminants through reductive transformation or adsorption, but there is a lack of comprehensive understanding regarding the sorption mechanisms and the factors influencing the efficiency of this process. A deeper understanding of these factors is crucial for developing sustainable and efficient water treatment strategies. This study focuses on magnetite nanopowder’s sorptive properties, examining critical factors such as pH, ionic strength, and competing anions that affect selenite removal. Sorption kinetics revealed an initial rapid selenite removal followed by a slower, time-dependent phase, suggesting a complex sorption mechanism. Chemisorption was considered the primary sorptive interaction, with diffusion playing a minor role, and was best described by the pseudo-second order kinetic model. Notably, pH significantly affected sorption efficiency and the suggested sorptive mechanism. Acidic conditions favored selenite removal due to formation of inner-sphere complexes, while alkaline conditions reduced efficiency due to repulsive interactions. Equilibrium sorption data were best fitted by the Langmuir model, with maximum sorption at pH 3, indicating that acidic conditions favor selenite removal. X-ray photoelectron spectroscopy (XPS) analysis ruled out the formation of reduced selenium compounds on the magnetite nanopowder surfaces. Additionally, Mössbauer spectrometry revealed that the nanopowder is not homogeneous and contains both magnetite and maghemite phases. Ionic strength and co-occurring ions showed minimal chloride impact but significant phosphate competitiveness due to its affinity for iron oxides. In conclusion, this study sheds light on the complex selenite sorptive interactions with magnetite nanopowder, emphasizing the dominance of chemisorption, especially in acidic solutions.