Langmuir Isotherm Research Articles

Synthesis and study of the inhibitory properties of a new Schiff base for C45 carbon steel in 1 M HCl

A newly Schiff base 1, 13-bis-[(4-dimethylamino) benzaldehyde 4, 7, 10-trioxatridecane-diimine] (DABT) was synthesized and characterized on the basis of the results of FT-IR, mass spectroscopy (MS), 1HNMR and 13CNMR. The desired performance of the organic compound DABT which is easy, inexpensive to prepare and eco-friendly, as a corrosion inhibitor for C45 carbon steel in 1 M HCl medium was evaluated using weight loss, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) measurements. The results suggest that the corrosion inhibition effectiveness increases with increasing inhibitor concentration and decreases with increasing temperature. The polarization experiments demonstrate that DABT exhibits the characteristics of a mixed-type inhibitor and follows the Langmuir isotherm in its adsorption behavior. Contact angle measurement revealed that the inhibitor on the surface of the carbon steel is hydrophobic. The synergistic effect of DABT has been investigated; inhibitory efficiency rises with increasing concentration of KI by competitive adsorption to form a layer of protection on the metal surface. Energy dispersive X-ray spectroscopy (EDS) combined with scanning electron microscope (SEM) was utilized to interpret the morphological study of the carbon steel surface. A good correlation was found between theoretical [Density functional theory (DFT), molecular dynamics simulation (MDS)] and experimental findings.

Synthesis of nano magnetic chitosan modified with acrylamide schiff’s base for simultaneous removal of Cu(II) and Co(II) from waste water samples

ABSTRACT A magnetic nano sorbent based on the functionalization of magnetic chitosan with acrylamide was synthesized for Cu(II) and Co(II) removal from wastewater samples. To characterize the magnetic nano sorbent, they have been applied from Fourier transform infrared spectroscopic analysis (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. The effective parameters of Cu(II) and Co(II) adsorption on magnetic nano sorbent such as pH of the solution, adsorbent dose, contact time and sample volume, were optimized. Also, the effective parameters on Cu(II) and Co(II) desorption conditions (type and volume of elution solvent) were optimized. The isotherms and kinetics models for the adsorption of Cu(II) and Co(II) on the magnetic nano sorbent were studied. The data were well-fitted with the Langmuir isotherm and pseudo-second-order model. The maximum adsorption capacities for Cu(II) and Co(II) were 165.4 and 159.9 mg g-1, respectively. Also, the thermodynamic parameters were studied. Application of magnetic nano sorbent for 4 times of use was acceptable. For the real samples, the percentage of recovery was higher than 97% and RSD (%) was between 1.4% and 2.7%. Finally, the magnetic nano sorbent exhibited high performance in removing the Cu(II) and Co(II) from wastewater samples.

Discrete Dynamic System Modeling for Simulated Moving Bed Processes

Although the simulated moving bed (SMB) process boasts advantages such as high productivity and low consumption, the cost of obtaining optimized parameters through practical experiments to control the separation process can be enormous due to its complex nonlinear characteristics. Consequently, the successful transformation of the SMB separation process into a mathematical dynamic model for computer simulation would greatly reduce the research costs associated with experimental studies. In this study, the Crank–Nicolson method was employed to discretize and dynamize the SMB process, enabling the simulation of processes under both linear and Langmuir isotherms. The results of the simulation experiments demonstrated the feasibility and high efficiency of this approach, thereby establishing a solid foundation for further advancements in online control strategies.

Synergistic effect of ZnO nanocomposite of Dodonea viscosa for corrosion inhibition in saline media

Abstract Dodonea viscosa-zinc oxide (DV-ZnO) nanocomposite was synthesized and characterized using Fourier transform infrared (FTIR), thermal gravimetric method (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS). The most abundant compounds in the plant extract were explored using gas chromatography-mass spectrometry (GC-MS). FTIR indicated the existence of the different functional groups, XRD showed that the nanocomposite has the hexagonal wurtzite shape of ZnO nanoparticles, SEM-EDS showed a size of 50 nm, and elemental analysis depicts the existence of the different elements in the extract, which confirms, along with TGA results, the formation of DV-ZnO nanocomposite. The nanocomposite synergistic effect was examined for anticorrosion capabilities using gravimetric, electrochemical, and surface analysis methods. Both the plant extract and the nanocomposite exhibited corrosion inhibition abilities. However, the incorporation of the plant extract with ZnO increased the inhibition efficiency by 20 %. Weight loss and electrochemical methods concluded an inhibition efficiency of 80 % for DV-ZnO nanocomposite. The inhibition of the nanocomposite is due to the adsorption of the inhibitor on the carbon steel surface, which was verified using X-ray photoelectron spectroscopy and scanning electron microscopy (SEM). The adsorption was found to follow both Langmuir and Temkin isotherms. Surface examination using atomic force microscopy (AFM) found that the carbon steel surface roughness was decreased from the sample submerged in an uninhibited medium (Sa = 121.20 nm) when adding DV-ZnO nanocomposite (Sa = 22.95 nm) and DV plant extract inhibitor (Sa = 54.73 nm).

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.

RSM versus ANN for modeling and optimization of magnetic adsorbent based on montmorillonite and CoFe2O4

A highly resourceful, environmentally benign, and recyclable magnetic montmorillonite composite (MMT/CF) was obtained through a simple one-step hydrothermal method and exhibited excellent Pb (II) removal. The as-synthesized adsorbent was then characterized by XRD, SEM–EDX, FTIR, BET, and TGA-DTA. The operating parameters including adsorbent dosage, initial Pb (II) concentration, solution pH, and time were studied. Also, a comparative approach was formed between response surface methodology (RSM) and artificial neural network (ANN) to optimize and model the removal efficiency of Pb (II) by MMT/CF. The results indicated that the ANN model was more precise and quite trusted optimization tool than RSM in consideration of its higher correlation coefficient (R2 = 0.998) and lower prediction errors (RMSE = 0.851 and ADD = 0.505). Langmuir isotherm provided the best fit to the experimental data, and the maximum adsorption capacity was 101.01 mg/g. Additionally, the kinetic studies showed that the pseudo-second-order model fitted well with the experimental data. The magnetic MMT/CF composite possesses high adsorption capacity and is suitable for reuse. Therefore, this study shows that MMT/CF composite can be a potential adsorbent in Pb (II) uptake from aqueous media.

An electrochemical, and surface studies of synthesized Gemini ionic liquid as corrosion inhibitor for carbon steel in petroleum field

In this work, we study the efficiency of N1, N3-dibenzyl-N1, N1, N3, N3-tetramethylpropane-1,3-diaminium chloride, as anticorrosion. This compound exhibits potential as a prospective remedy to stop the deterioration of carbon steel caused by corrosion in 1.0 M HCl. The synthesis of this compound is described in a comprehensive manner, and its composition is supported by a range of precise analytical approaches such as elemental analysis, and mass spectroscopy. Based on the findings of the investigation, the synthesized Gemini ionic liquid demonstrates a robust capacity to slow down the rate at which the metal corrodes. The Prepared compound was evaluation by electrochemical and morphology study. Our results revealed that elevating the inhibitor concentration led to an augmentation in inhibition effectiveness, reaching up to 94.8% at 200 ppm of the synthesized compound at 298 K. It is crucial to emphasize that the recently prepared Gemini ionic liquid is consistent with the Langmuir adsorption model and function as a mixed inhibitor, participating in the physio-chemisorption process of adsorption.

Gas Adsorption Mechanism on 2D Materials: The Hyperpolarizability Evolution Analyzed by Nonlinear Optics

AbstractWhile understanding the competitive adsorption behavior of gas sensor is important, it is yet to be unraveled. Especially for the influence of water molecules to the gas adsorbed on 2D materials. This study explores the potential of layered 2D materials as a candidate material for gas sensing, employing non‐destructive measurement, and second harmonic generation (SHG). The investigation focuses on analyzing oxygen, ammonia, and water vapor adsorbed on a WS2 surface by studying the evolutions in electric dipole and electric field. Leveraging the simplified bond hyperpolarizability model (SBHM), a foundation is established for gas sensors utilizing high‐quality 2D materials. This approach facilitates the detection of material modifications in response to environmental influences, including the inevitable water molecules. The obtained hyperpolarizability from SBHM exhibits remarkable consistency with Langmuir's adsorption model, confirming the physical adsorption in the system. In addition, the competitive effects between gases are explored by comparing experimental results with theoretical predictions based on Boltzmann distribution and density functional theory (DFT) calculations. This highlights the effectiveness of SHG and SBHM in studying gas adsorption on layered van der Waals materials.

Efficiency of magnetic zeolitic imidazolate framework-8 (ZIF-8) modified graphene oxide for lead adsorption.

Simple and efficient removal of Pb(II) ion from aqueous solution through adsorption has accelerated the development of many new composites to improve this popular method. In this study, the composites of graphene oxide (GO), zeolitic imidazolate framework-8 (ZIF-8), and magnetic materials were synthesized via coprecipitation method utilizing a different molar ratio between FeCl2 and FeCl3 of 1:0.5, 2:1, 3:1.5, and 4:2. The ZIF-8/GO was prepared via room temperature synthesis method prior to its further modification with magnetic materials for ease of separation. It was observed that the MZIF-8/GO2 of molar ratio 2:1 showed the best performance in adsorbing Pb(II) ion. As confirmed by FESEM image, it appeared to be ZIF-8 particles that have grown all over the GO platform and overlayed with Fe3O4 granular-shaped particles. The MZIF-8/GO2 successfully achieved 99% removal of Pb(II) within 10min. The optimum values obtained for the initial concentration of Pb (II) were 100mg/L, pH of 4 to 6, and adsorbent dosage used was 10mg. The Langmuir isotherm and the pseudo-second-order kinetic model were deemed suitable to evaluate the adsorption of Pb(II) using MZIF-8/GO2. Results showed that MZIF-8GO2 achieved a maximum adsorption capacity of 625mg/g of Pb(II) adsorption. All parent materials demonstrated a good synergistic effects, while exhibiting a significant contribution in providing active sites for Pb(II) adsorption. Therefore, this ternary composite of MZIF-8/GO2 is expected to be a promising adsorbent for Pb(II) adsorption from aqueous solution with an added value of ease of post phase separation using external magnetic field.

Enhanced adsorption and removal of Cd(II) from aqueous solution by amino-functionalized ZIF-8

Zeolite imidazolate framework-8 (ZIF-8), which is a special subgroup of metal–organic frameworks (MOFs), was synthesized and modified by ethylenediamine (ZIF-8-EDA) to prepare an efficient adsorbent for the high sorption of Cd2+ ions from solution. The synthesized and modified ZIF-8 (ZIF-8-EDA) were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, Brunauer–Emmett–Teller (BET), field emission scanning electron microscopy (FE-SEM) with energy dispersive spectroscopy (EDS), and transmission electron microscopy (TEM) analysis. The optimum conditions for dosage of adsorbent, initial ion concentration, pH, and contact time were 0.05 g/l, 50 mg/l, 6, and 60 min, respectively, for cadmium ion sorption from aqueous solutions with a removal efficiency of 89.7% for ZIF-8 and 93.5% for ZIF-8-EDA. Adsorption kinetics and equilibrium data were analyzed using the Langmuir and Freundlich equations. The Langmuir model fitted the equilibrium data better than the Freundlich model. According to the Langmuir equation, the maximum uptake for the cadmium ions was 294.11(mg/g). The calculated thermodynamic parameters (ΔG°, ΔH°, and ΔS°) indicated that the adsorption process was feasible, spontaneous, and endothermic at 20–50 °C. Based on the results, the amino functionalized ZIF-8 had improved adsorption performance due to the replacing of the starting linker with organic ligands that had effective functional groups, leading to chemical coordination due to the interaction of metal ions with the non-bonding pair of electrons on the N atoms of the amino functional group. The selectivity toward metal ion adsorption by ZIF-8-EDA was Cd2+ > Pb2+ > Ni2+‏.

One-pot synthesis of novel polyvinylphosphonic acid hydrogels for efficient separation of low-enriched uranium in water

Uranium extraction from seawater and the treatment of radioactive wastewater has traditionally been a hot topic. Herein, p(VPA-AM)n solid hydrogels with high uranium extraction properties based on vinylphosphonic acid (VPA) were successfully prepared by one-step copolymerization for the first time. The batch adsorption experiments demonstrated that p(VPA-AM)n has strong uranium chelating ability, fast uranium adsorption kinetics (within 200 min) and high uranium adsorption capacity (644.67 mg/g), and its adsorption behavior conforms to the pseudo-second-order kinetic model and the Langmuir adsorption isotherm model, which is a spontaneous heat-absorbing chemical monolayer adsorption process. After 15 adsorption–desorption tests, the adsorption capacity was kept above 96 % of the original capacity, and the uranium extracted from the salt lake water achieved at 3.56 mg/g, which showed superb behavior in treating complex uranium systems. Mechanism studies revealed that the strong interaction between UO22 + and −PO43- dominated the adsorption and the robust complexation might have led to the electron transfer in the structure. The maximum uranium removal rate of p(VPA-AM)n in simulated seawater reached 90 %, and the simple in situ zinc oxide-modified p(VPA-AM)n hydrogel showed good anti-biosludge properties against three common bacteria (E. coli, B. subtilis and S. aureus), which has a great potential for application in seawater uranium extraction and uranium wastewater treatment.

Phosphorus adsorption from aqueous solutions using different types of cement: kinetics, isotherms, and mechanisms.

Exploring low-cost and high-performance phosphorus (P) adsorbents is key to controlling P contamination in water. This study evaluated the P adsorption performance of three types of cement: Ordinary Portland cement (OPC), Portland slag cement (PSC), and Portland pozzolana cement (PPC). Furthermore, SEM-EDS, XRD, XPS, and FTIR were employed to reveal the adsorption mechanism. The results showed that the pseudo-second-order model exhibited higher regression coefficients than the pseudo-first-order model, indicating that chemisorption dominated the adsorption process. The Langmuir equation fitted the P adsorption data well, with maximum P adsorption capacities of 245.8, 226.1, and 210.0 mg g-1 for OPC, PSC, and PPC at 25 °C, respectively. P adsorption capacities decreased gradually with increasing initial pH and reached their maximum values at pH 3. The anions of F-, CO32-, and SO42- negatively affected P adsorption due to the competitive adsorption with Ca2+. The results of XPS, XRD, and FTIR confirmed that Ca-P precipitates (i.e., hydroxyapatite) were the main removal mechanism. A real domestic sewage experiment showed that 0.6 g L-1 OPC effectively reduced the P concentration from 2.4 to below 0.2 mg L-1, with a dosage cost of 0.034 $ per ton. This study indicated that cement, as a low-cost and efficient P adsorbent, has great potential for application in removing P from acidic and neutral wastewater.

Comparative adsorption of cationic and anionic dye by using non-activated Black Plum seed biochar for aquatic phase: Isotherm, kinetic and thermodynamic studies

Industrial dye effluents play a major role in water pollution. Textile and leather industries are one of the important sectors that pollute the water by discharging many harmful cationic and anionic dyes during the dyeing process. This study aims to compare the dye removal efficiency of Black Plum seed biochar for the cationic and anionic dyes. The non-activated biochar was prepared through pyrolysis of Black Plum seed powder at 5700 C. The sample's surface chemistry was understood using various characterization techniques like Field Emission Scanning Electron Microscopy (FESEM), Energy-dispersive X-ray spectroscopy (EDS), Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), Raman-Spectroscopy and Zeta-potential. The experiments were successfully performed by conducting a batch adsorption study at different parameters such as pH, concentration, contact time and temperature. The coefficients of different isotherms and kinetics models were evaluated for non-linear study and the thermodynamic model was also applied. The maximum adsorption capacity was obtained as 42.39 mg/g for Crystal Violet (CV) dye and 6.22 mg/g for Eosin Blue (EB) dye by using the Langmuir isotherm model. Hence, the Black Plum seed biochar (BPSB) has superior adsorption capacity for the cationic dye CV ( removal - 98%) as compared to the anionic dye EB ( removal - 65%) at optimum parameters. Therefore, it is concluded that the BPSB is a natural toxin-free biosorbent and it can be used for the remediation of dyes from industrial wastewater.

Aqueous removal of Cr(VI) by Citrus sinensis juice-coated multi-walled carbon nanotubes

AbstractA novel adsorbent was prepared from multi-wall carbon nanotubes (MWCNTs) and Citrus sinensis juice extract-modified MWCNTs (OJMW) and characterized using scanning electron microscopy (SEM), Fourier transform infrared spectra (FTIR), X-ray diffractometer (XRD), BET and thermogravimetric analysis. The results showed that the nanotubes exhibited good surface area, pore size, functional groups, and robust stability at elevated temperatures (308 and 313 K). The adsorbent was applied in water for the sequestration of Cr(VI). The adsorption of Cr(VI) on MWCNTs and OJMW was influenced by factors of adsorption. Optimum removal of Cr(VI) was attained at 180 min contact time, 0.05 g adsorbent dose, and solution pH 2 for MWCNTs and OJMW. The kinetic behaviour of the Cr(VI) adsorption onto MWCNTs and OJMW was governed by the pseudo-first-order and pseudo-second-order kinetic model, respectively. The equilibrium data obtained for the uptake of Cr(VI) onto MWCNTs and OJMW fitted satisfactorily with Freundlich and Langmuir isotherm models, respectively. Meanwhile, MWCNTs and OJMW exhibited monolayer adsorption capacities (qmax) of 44.72 and 12.26 g g−1, respectively, at 298 K. The adsorption process was spontaneous and feasible. The direction of energy flow in the uptake of Cr(VI) onto OJMW and MWCNTs followed endothermic and exothermic adsorption processes, respectively. The adsorption–desorption experiments showed that OJMW had good regenerative abilities.

Efficient wastewater decontamination using magnetic bentonite-alginate beads: A comprehensive study of adsorption dynamics, regeneration, and molecular interactions

This study enhances wastewater treatment methodologies by developing magnetic bentonite-alginate beads (MBent-A beads) for adsorbing methylene blue (MB) from aqueous solutions. Experimental and computational analyses were employed to evaluate the beads' adsorption efficiency, utilizing characterization techniques including Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), point of zero charge (pHpzc), Brunauer-Emmett-Teller method (BET), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS) to examine the composite’s morphology and chemistry. Findings reveal a significant adsorption capacity with the beads' specific surface area at 3.94 m2/g and a maximum adsorption capacity of 774.32 mg/g. Adsorption kinetics adhered closely to the pseudo-second-order model, indicating a rapid adsorption process, while Langmuir isotherm analysis confirmed a uniform monolayer adsorption and temperature-dependent capacities. Thermodynamic analysis showed the adsorption process to be spontaneous and exothermic, reflecting a strong affinity between MB molecules and the bead surface. The beads demonstrated durability with more than 90% removal efficiency after five regeneration cycles, highlighting a minimal decrease from 98.54% to 90.60%. In-depth theoretical investigations using density functional theory (DFT), frontier molecular orbital (FMO), reduced density gradient (RDG), and quantum theory of atoms in molecules (QTAIM) analyses identified van der Waals forces and hydrogen bonding as primary interactions driving the adsorption. The synthesis of MBent-A beads and their confirmed efficacy in dye adsorption integrates experimental research with theoretical modeling, offering a robust solution for treating dye-contaminated wastewater and underlining the potential of MBent-A beads in environmental remediation.

Unleashing the potential of Cajanus cajun biochar polymer composite for Cu (II) removal: mechanism, modification, and application.

This study introduces a cost-effective approach to fabricating a porous and ionically surface-modified biochar-based alginate polymer networks composite (SBPC) through air drying. The study critically analyzes the role and concentrations of various components in the success of SBPC. Characterization techniques were employed to evaluate the microstructure and adsorption mechanism, confirming the ability of the adsorbent's carboxyl and hydroxyl groups to eliminate various heavy metal ions in water simultaneously. The SBPC demonstrated high copper binding capacities (937.4mg/g and 823.2mg/g) through response surface methodology (RSM) and column studies. It was also influential in single and natural systems, exhibiting competitive behavior and efficient removal of Cu2+. The Langmuir isotherm and pseudo-second-order kinetics strongly correlate with experimental data, with R2 values of 0.98 and 0.99, respectively. SBPC showed remarkable stability, up to 10 desorption cycles, and achieved 98% Cu2+ adsorption efficiency and 91.0% desorption. Finally, the cost analysis showed a cost of 125.68 INR/kg or 1.51 USD/kg, which is very low compared to the literature. These results highlight the potential of SPBC and show that it provides an efficient and cost-effective solution for removing Cu2+ from a real system.

Greenly synthesised novel microporous ZnO/GO for adsorption of methyl orange and malachite green

ABSTRACT This study presents a greenly synthesised novel nanocomposite composed of Zinc Oxide (ZnO) and Graphene Oxide (GO) for the adsorption of dyes from aqueous solutions. The nanocomposite was synthesised using algae thus representing a green and eco-friendly method, ensuring minimal environmental impact. The physical characterisation of zinc oxide and graphene oxide nanocomposite (ZnO/GO) was done using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), Fourier transform infrared spectroscopy (FT-IR), Zeta Potential, and Particle Size Analyzer (PSA). The pore diameter of the ZnO/GO was 1.801 nm, and its total surface area was 54.062 m2/g. The nanocomposite’s adsorption performance was systematically investigated through batch adsorption experiments. With an adsorption efficiency of 296.73 mg/g and 259.74 mg/g for MO and MG, the Langmuir isotherm model outperforms the Freundlich isotherm model in terms of adsorption. The pseudo-second-order model having an R2 value of 0.99 for both MO and MG, offers a more convincing explanation of adsorption than the pseudo-first-order model. The results demonstrated rapid adsorption kinetics and high adsorption capacities for both cationic and anionic dyes. Additionally, the ZnO/GO has a high reusability without significant degradation. The sustainable nature of the nanocomposite was emphasised by its efficient dye removal, reusability, and minimal secondary waste generation.

Modified powder of Corchorus capsularis as a new adsorbent for removal of tetracycline group antibiotic from water

AbstractThis study prepared a novel adsorbent from Corchorus capsularis modified powder for the removal of the tetracycline group (tetracycline ‐TC, oxytetracycline ‐OTC, chlortetracycline ‐CTC) in aqueous solution. Corchorus capsularis powder was pre‐treated with 15% sodium hydroxide (COC), then reformed by a mixture of 0.15 mol L−1 sodium bisulfide (SB) and 0.2 mol L−1 ammonium peroxydisulfate (APS). This adsorbent was embedded with monoacrylamide (AM) at ratio AM/COC = 1/1 at 60 °C for 2.5 h. After modification with AM (BTA), the surface area of the adsorbents increased from 1.53 to 2.79 m2 g−1, while the pore size of the adsorbents decreased from 36.95 to 11.85 nm. The study also investigated the effects of pH, adsorbent dose and temperature on the adsorptive removal process. Tetracycline concentrations were determined using liquid chromatography–tandem mass spectrometry (LC–MS/MS). The kinetics and isotherms of adsorption performance were examined using a variety of models, including pseudo‐first‐order kinetic (PFO), pseudo‐second‐order kinetic (PSO), Freundlich, Langmuir, and Dubinin–Radushkevich isotherms (DRM). The experimental data fitted very well with the pseudo‐second‐order kinetic model. The maximum adsorption bulks of TC, OTC, CTC following Langmuir isotherm model were 1.25, 0.83, 1.43 mg g−1, respectively. The adsorption constants Kp of TC, OTC, and CTC from the Freundlich isotherm model were 15.36, 21.80, and 22.08 mg1−nLng−1, respectively. The mean free energy E (kJ mol−1) of TC, OTC, and CTC from DRM was 4.35, 4.20, and 4.57, respectively. The results indicated that modified Corchorus capsularis powder had significant potential as a new adsorbent material for removing antibiotics from aqueous solutions.

A Sustainable Approach for Enhancing Cationic Dyes Adsorption in Single and Multiple Systems using Novel Nano Ferrites Modified with Walnut Shell

AbstractWalnut shell has been used in various experimental studies for different dyes removal, but it is exciting to study the adsorption behaviour of bio‐waste (walnut shell) in combination with spinel zinc ferrite which resulted in the formation of a novel material having magnetic properties and help in easy separation after the wastewater treatment. Novel magnetic walnut shell zinc ferrite (WSZF) composite has been synthesized and used to remove Malachite Green and Methylene Blue from aqueous solution in single and binary dye systems. Different techniques have been used to characterize the composite such as Fourier Transform Infrared Spectroscopy, X‐Ray Diffraction, Field Emission Scanning Electron Microscopy, Energy Dispersive Spectroscopy, Thermogravimetric Analysis and pHzpc. Adsorption of dyes were studied to see the effect of time, pH, adsorbent dose, dye concentration and temperature. The Lagergren pseudo second order model fitted well among various kinetic models employed. Langmuir adsorption isotherm best fitted with maximum adsorption capacities of 86.20 and 169.5 mg/g in single dye and 23.92 and 18 mg/g respectively in binary dye system for Malachite Green and Methylene Blue. Process was spontaneous and ΔH° were found positive, confirmed endothermic process of adsorption. The composite‘s regeneration capacity was studied for five cycles and at the end of five cycle the efficiency of the material was found to be around 80 % for both single as well as binary dye systems. It is concluded that the chosen WSZF will be the optimum solution for cationic dyes removal.

Chitin extraction from crab shells and synthesis of chitin @metakaolin composite for efficient amputation of Cr (VI) ions

The present research study combines chitin from shrimp waste with the oxide-rich metakaolin. Metakaolin is a blend of mixed oxides rich in silica and alumina with good adsorbent properties. The chitin@metakaolin (CHt@M.K.) composite was synthesized and characterized using FTIR, SEM, TGA, XRD and XPS techniques. Cr(VI) removal studies were compared for chitin and CHt@M.K. through adsorption. It was found that the adsorption capacity of CHt@M.K. is 278.88 mg/g, almost double that of chitin, at pH 5.0 in just 120 min of adsorption. Isotherm models like Langmuir, Freundlich, Temkin and Dubinin–Radushkevich were investigated to comprehend the adsorption process. It was revealed that Langmuir adsorption isotherm is most suitable to elucidate Cr(VI) adsorption on CHt@M.K. The adsorption kinetics indicate that pseudo first order was followed, indicating that the physisorption was the process that limited the sorption process rate. The positive enthalpy change (20.23 kJ/mol) and positive entropy change (0.083 kJ/mol K) showed that the adsorption process was endothermic and more random at the solid-liquid interface. The negative free energy change over entire temperature range was an indicator of spontaneity of the process. Apart from all these, the non-covalent interactions between Cr(VI) and composite were explained by quantum calculations based models.