Methyl Green Research Articles

Binary and Ternary Deep Eutectic Solvents for Methylene Green Electropolymerization on Multiwalled Carbon Nanotubes: Optimization, Characterization and Application.

Choline chloride (ChCl) based binary and ternary deep eutectic solvents (DES) were evaluated for methylene green electropolymerization with oxalic acid (OA) and ethylene glycol (EG) as hydrogen bond donors. Binary DES ChCl : OA in molar ratios 1 : 1 and 2 : 1 and ChCl : EG 1 : 2 and ternary DES (tDES) in different molar ratios and percentages of water were evaluated. The highest polymer growth was in ChCl : OA : EG-tDES with 13% added water, that had a lower viscosity and higher ionic conductivity when associated with HCl as dopant. This enhanced the formation of more cation radicals and, consequently, more polymer formation. The PMG/MWCNT/GCE-tDES sensor was successfully applied to the simultaneous determination of 5-aminosalicylic acid (5-ASA) and acetaminophen (APAP) by differential pulse voltammetry in the concentration range 1 μM-200 μM, with detection limits of 0.37 μM and 0.49 μM for 5-ASA and APAP, respectively. The sensor demonstrated good repeatability, reproducibility and stability, and was successfully applied in pharmaceutical formulations.

Histochemical Analysis of DNA and RNA Identified by Methyl Green - Pyronin ‘Y’ Method and Feulgen’s Reaction Staining in Liver of Channa Punctatus

The light microscopy was to identify cells, storage products, tissue deposits, and microbial pathogens. The Assessment of surrounding tissue with special stains may reveal aspects of interest for the tissue. We illustrate the expected staining characteristics of control Channa punctatus liver tissue with Methyl Green -Pyronin ‘Y’ and Feulgen’s Reaction stains. The aim of this study was to characterize the normal structure of the liver of Channa punctatus, a carnivorous freshwater fish found in Hasanparthy Lake, using gross anatomy, histology and histochemistry. Anatomically, the liver presents C-shaped and only two lobes smaller right and bigger left. The gallbladder is located in right lobe and shows elongated shaped. Histological analysis demonstrated that the hepatic parenchyma is made of two hepatocytes plates surrounded by sinusoids. The fish moreover pancreatic tissue was observed in visceral portion of liver, formed by exocrine pancreatic tissue and islet organ, constituting an extrahepatic pancreas. The nucleic acids content in different tissues in the freshwater fish of Channa punctatus. The fish were scarified and the tissues such as liver and Pancreas removed and processed for determination of nucleic acids. The results obtained in the present study may provide a contribution to the knowledge of the characteristics of nucleic acid as parameters of estimation of DNA and RNA levels in Liver of the fish.

Confocal image of three oxoaporphine alkaloids in cancer cell lines and their interaction with DNA by multispectroscopic and molecular docking techniques

Dicentrinone (Di), liriodenine (Li) and lysicamine (Ly) are three natural oxoaporphine alkaloids (OAs), which revealed significant biological activity such as anticancer, anti-inflammatory and antimicrobial activities and were considered as potential lead compounds for the development of new clinical chemicals. In the present study, confocal laser scanning fluorescence microscopy observation demonstrated these three natural OAs could traverse inside of the nucleus and get an opportunity to interact with DNA. Their interaction properties with DNA were then investigated simultaneously by two spectral fluorescent probes of ethidium bromide (EB) and methyl green (MG), as well as UV–vis absorption and cyclic voltammetry measurements, and further verified by the molecular docking analysis. Results indicated Di and Li were distinctly classified as the intercalative molecules to DNA, however, Ly was confirmed with a mixed-mode binding of partial intercalation and groove affinity. Their binding ability was revealed as the follows: Di ≥ Li > Ly, which was correlated with their structural changes. Thermodynamic studies revealed the binding process of Li and Ly with ctDNA was all spontaneous, the hydrophobic interaction was the major binding force for Li-ctDNA complex, however, the interaction between Ly and ctDNA relied on both hydrophobic and hydrogen binding force. Molecular docking provided detailed computational interaction of Di, Li and Ly with DNA, which proved the intercalation binding of Li-DNA complex and Di-DNA complex stabilizing mainly by the π-π binding force, however, apart from a small quantity of π-π interaction, another binding force in the Ly-DNA complex mainly was supplied from the weaker Pi-Alkyl, hydrogen bond and Pi-Anion interactions.

Bentonite clay reinforced alginate grafted composite hydrogel with remarkable sorptive performance toward removal of methylene green

The rapid industrial progress in today's world has led to an alarming increase in water pollution caused by various contaminants such as synthetic dyes. To address this issue, a new hydrogel sorbent, BC-r-Na-Alg-g-p(NIPAm-co-AAc), was developed by combining bentonite clay, sodium alginate, and poly(N-isopropyl acrylamide-co-acrylic acid) through one-pot free radical polymerization at 60 °C. The developed sorbent was characterized using several analytical techniques including SEM, FTIR, TGA, UTM, and swelling studies. The swelling capacity of the sorbent was observed to increase remarkably with an increase in pH, reaching a maximum of 9664 % at pH 11. In batch mode sorption experiments, the sorbent's performance toward methylene green (MG) was investigated by analysing the effects of contact time, pH, temperature, and concentration. The experimental data were fitted to pseudo-second-order kinetic and Langmuir isotherm models, indicating chemisorption as the dominant interaction mode between the anionic sorbent and cationic MG. However, physisorption may also occur to a lesser extent, indicated by the significant R2 of the pseudo-first-order kinetic and Freundlich isotherm models. Additionally, the sorbent exhibited very little decrease (approximately 5 %) in sorptive performance for six sorption-desorption cycles. Overall, the facile fabrication, excellent swelling (9664 %), promising sorption performance (2573 mg.g−1), and good recyclability (6 cycles) make the developed sorbent a potential candidate for various industrial applications.

Efficient adsorptive removal of methyl green using Fe3O4/sawdust/MWCNT: Explaining sigmoidal behavior

The 4R concept (reduce, reuse, recycle and repurpose) in water management necessitates innovative adsorption techniques that utilize sustainable and natural materials. This study investigates the use of natural sawdust embedded in magnetic iron oxide to treat wastewater. The performance of the newly synthesized Fe3O4/sawdust adsorbent was also compared to the native Fe3O4 and Fe3O4/MWCNT. Methyl Green (MG) was used as a model pollutant due to its wide use and potential toxicity. The new adsorbents demonstrated a high removal efficiency that exceeds 97 % under ambient conditions. The study investigates the effect of pH on adsorption, revealing a significant shift in removal efficiency as pH increases, with an optimal pH of around 7. The pH dependence is explained based on the point-of-zero-charge of the Fe3O4 adsorbent and the structure of the dye. The thermodynamic parameters (ΔH°, ΔS°, and ΔG°) of adsorption were determined through a temperature study. The adsorption equilibrium was found to be endothermic, therefore preferring elevated temperatures. Because the adsorption data of the study exhibited S-shaped-like curves, sigmoidal models were used to describe the adsorption isotherms. This provided new insights into the competitive adsorption mechanisms acting on the heterogeneous Fe3O4/sawdust surfaces. The kinetics study indicates rapid and efficient adsorption with pseudo-second-order reaction. The half-life of the reaction was as low as 4.8 min. The findings suggest a rapid, highly efficient and sustainable method to remove organic pollutants from wastewater.

Removal of two cationic dyes by adsorption on F400 commercial activated carbon

In this investigation, we studied the removal of two cationic dyes, methyl green MG and malachite green Mc G, by a commercial adsorbent. This adsorbent is a F400 activated carbon with a specific surface area of 1203 m2. g-1, which is expected to be high compared with ordinary adsorbents. Adsorption tests were carried out on both dyes in batch mode. The results show that both kinetics are fast, with equilibrium reached after 20 minutes and 30 minutes respectively for Methyl Green and Malachite Green. The kinetics of both dyes are well adapted to pseudo-second order, and for the intraparticle diffusion model, two lines can be distinguished for each dye, proving the existence of two adsorption steps. The isotherm for this system reveals an L-type shape for both dyes, in line with the classification of Giles & al. so there is little competition for sorption sites between solvent and adsorbate. The adsorption isotherms for methyl green by PAC obeyed the Langmuir, Freundlich and Temkin models, while that for malachite green followed only the Langmuir isotherm, with a much higher maximum amount.

Wavelength-selective, time-resolved, and visible-light-responsive multicolor switching systems for multistate dynamic information encryption

Visible-light-responsive photoreversible multi-color switching systems (PMCSSs) are attractive to meet the advanced demands in dynamic information encryption. Particularly, PMCSSs with wavelength-selective and time-resolved color switching are highly important but underexplored. Here, a new strategy is proposed to realize wavelength-selective, time-resolved, and visible-light-responsive PMCSSs by integrating acetamide ligand-capping CdS (CdS-NH2) nanoparticles and various redox dyes in solid films for multistate dynamic information encryption. The –NH2 groups of surface-bounded CH3CONH2 act as sacrificial electron donors for scavenging photogenerated holes to endow the CdS-NH2 nanoparticles high photoreductive ability and activity in a broad visible light range from 400 to 515 nm, thus enabling the long-waited wavelength-selective multicolor switching via coupling the wavelength-dependent photoreductivity of CdS-NH2 nanoparticles and the discoloration kinetics of redox dyes, such as methylene blue (MB) and phenosafranine (PS). Moreover, the time-dependent color switching during recoloration process of the color switching system can be modulated by tuning the oxidation kinetics of MB and methylene green (MG), enabling time-resolved dynamic imaging characteristics. Based on the unusual properties of the PMCSSs, a kind of wavelength-selective and time-resolved codes are designed for advanced dynamic information encryption. This work provides new guidance for developing of new PMCSSs for information encryption with high security requirements.

Z-scheme based photoactive ZnO:TiO2:CdO:g-C3N4 nanocomposites for advance oxidation process

Z-scheme-based hybrid [(ZnO0.40:0.60TiO2):CdO1.00]:g-C3N4] nanocomposites (NCs) were synthesized by sol-gel precipitation and thermal polycondensation methods. Microscopic FE-SEM images varied from a compact crystal-like structure to a mesoporous sheet-type structure. XRD patterns confirmed the polycrystallinity for all samples. Meanwhile, the g-C3N4 interacts extensively with Zn+2 and Cd+2. The optical bandgap increased from 2.12 eV to 2.25 eV with the addition of g-C3N4 concentration. Z-scheme [(ZnO0.40:0.60TiO2):CdO1.00]:[g-C3N4] NCs of the particular composition named ZTCG4 showed the highest photocatalytic activity and degraded the methylene blue (MB), methyl green (MG), and methyl orange (MO) to be 99.7 %, 99.8 %, and 99.9 %, respectively, under the illumination of the visible light. Mineralized factors: chemical oxygen demand (COD) and biochemical oxygen demand (BOD) achieved the maximum removal efficiencies of 89.4 % and 88.9 % for the sample g-C3N4. Prepared photocatalysts can be utilized to remove the organic pollutants from the drainage systems under visible light exposure.

Design of silver-zinc-nickel spinel-ferrite mesoporous silica as a powerful and simply separable adsorbent for some textile dye removal

Silver-zinc-nickel spinel ferrite was prepared by the co-precipitation procedure with the precise composition Ag0.1Zn0.4Ni0.5Fe2O4 for bolstering pollutant removal effectiveness while upholding magnetic properties and then coated with a mesoporous silica layer. The surface characteristics and composition of Ag0.1Zn0.4Ni0.5Fe2O4@mSiO2 were confirmed using EDX, FT-IR, VSM, XRD, TEM, SEM, and BET methods. The surface modification of Ag-Zn-Ni ferrite with a silica layer improves the texture properties, where the specific surface area and average pore size of the spinel ferrite rose to 180 m2/g and 3.15 nm, respectively. The prepared spinel ferrite@mSiO2 has been utilized as an efficient adsorbent for eliminating methyl green (MG) and indigo carmine (IC) as models of cationic and anionic dyes from wastewater, respectively. Studying pH, Pzc, adsorbent dosage, dye concentration, and temperature showed that efficient removal of MG was carried out in alkaline media (pH = 12), while the acid medium (pH = 2) was effective for IC removal. Langmuir isotherm and pseudo-second-order kinetics were found to be good fits for the adsorption data. Both dyes were adsorbed in a spontaneous, endothermic process. A possible mechanism for dye removal has been proposed. The adsorbent was effectively recovered and reused.

N–ZnO/g-C3N4 nanoflowers for enhanced photocatalytic and electrocatalytic performances

In this study, CNNZO (N–ZnO/g-C3N4) nanocomposites were synthesized via a facile hydrothermal method and characterized using XRD, FTIR and FESEM. The resulting N–ZnO nano-needles and plate-like structures, anchored onto g-C3N4 agglomerates, formed distinctive nano-flower topography. CNNZO demonstrated superior photocatalytic activity compared to CN and N–ZnO, achieving ∼98 % degradation of Methylene Blue, 85.53 % of Methyl Green and 87.29 % of Methyl Orange under visible light irradiation within 90 min. This enhanced performance is attributed to the unique morphology of CNNZO, which promotes efficient charge carrier transfer and inhibits recombination. Additionally, CNNZO exhibited improved electrocatalytic activity with smaller HER and OER potentials. This study underscores the potential of CNNZO nanocomposites as effective catalysts for the degradation of organic contaminants and hydrogen and oxygen evolution for energy production.

Nano clinoptilolite zeolite as a sustainable adsorbent for dyes removal: Adsorption and computational mechanistic studies

Clinoptilolite, a naturally occurring zeolite with unique adsorption properties, is investigated in its nanoscale form as a sustainable adsorbent for effectively removing contaminant dyes, rhodamine B (RhB), malachite green (MG), and methyl green (MeG), from aqueous solutions. The nano clinoptilolite was prepared by ball milling and characterized using various techniques including XRD, FTIR, SEM, TGA, BET, and zeta potential to confirm its structure, functional groups, porous morphology, thermal stability, surface area and pore size distribution, and surface charge, respectively. The nano clinoptilolite has a crystalline size of 19.5 nm, determined by XRD. Its average hydrodynamic size in water is 285 nm, measured by dynamic light scattering. Adsorption experiments were carried out to evaluate the dye removal efficiency under various conditions such as pH, zeolite dose, dye concentrations, and contact time. The equilibrium adsorption data were fitted with different isotherm models such as Freundlich, Langmuir, Langmuir-Freundlich, and Sips; and the kinetics adsorption data were fitted with pseudo-first-order, pseudo-second-order, mixed-order, and Avrami models. Nanosized clinoptilolite exhibited a high maximum adsorption capacity for MG (191.36 mg MG/g at pH 5.0), exceeding a previous report by 336 % (43.86 mg MG/g). RhB adsorption capacity on zeolite was 58.02, 24.28 mg/g at pH 3.0, 7.0, and MeG was 162.94 mg/g at pH 7.0. Finally, Monte Carlo and molecular dynamics simulations were used to elucidate the specific binding sites, adsorption energies, and mechanisms involved in the removal process.

Degradation of bromothymol blue and methyl green from aqueous media by Photo-Fenton: comparison between UV-lamp and sun irradiation

Abstract The degradation of two textile dye molecules was studied using photochemical processes, both in the absence and presence of light. Various methods were employed, including photolysis/UV, combined H2O2/UV photolysis, Fe2+/UV treatment, Photo-Fenton/UV at 350 nm and Photo-Fenton with solar irradiation. The decolorization efficiency of dyes in aqueous solution was evaluated for two specific dyes: Bromothymol Blue (BTB) and Methyl Green (MG). These experiments were carried out in batch mode. The results demonstrated a synergy between light irradiation and the presence of Fenton’s reagents, such as hydrogen peroxide and divalent iron. In addition, it was demonstrated that direct solar irradiation can be used without specific devices to achieve high efficiency at low cost. In the first part, we checked the impact of the various operating parameters. Reaction efficiencies were compared for the same system in the dark and under the assistance of an artificial or solar light source. In the second part, we studied the parameters of the Photo-Fenton process, such as the initial pH of the solution, the initial concentrations of oxidant, iron catalyst, and dye under irradiation from either light source. Whereas the mere photolysis without Fenton’s reagents allowed decolorization yields below 26 %, addition of the oxidant (H2O2) or the catalyst (Fe(II) species amplified the treatment efficiency. However, the presence of both H2O2 and Fe(II) under light irradiation was shown synergetic with yields ranging from 72 to 85 % depending on the dye worked and the light source: because of its broader spectrum in the UV domain, solar irradiation led to the highest decolorization yields. The above results were obtained for well-defined proportions of dye and reagents: for a 20 mg/l dye solution, Fe(II) catalyst concentration equal to 10−3 M, peroxide concentration of 5.10−2 M and a pH of 3. These conditions allowed optimal production of OH· radicals, allowing high efficiency in systems using solar irradiation.

Green synthesis of magnetic silver nanocomposite: the photocatalytic performance of nanocomposite to decolorize organic dyes

ABSTRACT The magnetite-silver nanocomposites (Fe3O4-Ag NCs) were synthesized via a facile and green process by Citrus sinensis peel extract. The deposition of silver nanoparticles (NPs) was confirmed by observing an absorption peak at the maximum wavelength at 422 nm in the suspension solution of samples, which is related to silver surface plasmon resonance (SPR). The characteristic diffraction patterns of Fe3O4 and Ag phases were characterized utilizing the XRD patterns and the average size of the crystals was 21 nm. The photocatalytic behavior of Fe3O4-Ag NCs was studied for the destruction of three organic dyes methyl green (MG), methyl orange (MO), and methylene blue (MB) below UV radiation. The effect of the amount of photocatalyst and volume of hydrogen peroxide as an oxidant in the process of dye degradation was also investigated. The complete degradation time of dyes MB, MG, and MO under UV irradiation in the presence of 0.002 g Fe3O4-Ag NCs were 57, 33, and 49 min, respectively. The time of degradation reactions showed the high photocatalytic performance of Fe3O4-Ag NCs. These results proved that the synergistic effect of magnetite in the role of supporting the silver NPs was a significant contribution to the excellent decolorization behavior of Fe3O4-Ag NCs.

A high-performance TFN membrane prepared by a novel PE support layer, a polydopamine interlayer, and a doped MoS2 quantum dots@ZnO nanocomposites-incorporated polyamide active layer

Herein, thin film nanocomposite (TFN) membranes were prepared with excellent chemical stability and separation performance for organic solvent nanofiltration (OSN) applications. The support membrane was synthesized via a new approach, in which a blend of two immiscible polymers, i.e. high density polyethylene (HDPE)-polystyrene (PS), which were compatibilized with styrene-ethylene-butylene-styrene (SEBS), was prepared through mixing by a Brabender, followed by fabricating blend sheets through a hot press machine. The PE support was then prepared by extracting the PS/compatibilizer phase from the blend sheet. The hydrophilicity of the PE support membrane was considerably enhanced with a polydopamine (PDA) layer. Different nanoparticles including nanoflower (NF) ZnO, nanosphere (NS) ZnO, MoS2 Quantum dots-nanoflower ZnO nanocomposite (QDs@NF ZnO), and MoS2 Quantum dots-nanosphere ZnO nanocomposite (QDs@NS ZnO) were incorporated into the polyamide (PA) active layer of the membranes to enhance the performance of the TFN membranes. The separation performance of the TFN membranes was investigated for rejecting different dyes dissolved in methanol. Our results demonstrate outstanding separation performance, with a dye rejection of 99.6 %, 99.6 %, 99.8 %, and 99.9 % for methylene blue, crystal violet, rhodamine B, and methyl green, respectively. Additionally, the TFN membranes incorporated with QDs@NF ZnO nanoparticles showed great solvent resistance, with a methanol permeance up to 6.7 L/m2.h.bar after activation with dimethylformamide.

Investigating the adsorption of Malachite green and Methyl green onto synthesized Ni0.5Zn0.5Fe2O4 spinel ferrites

Nano-sized Ni0.5Zn0.5Fe2O4 spinel ferrites were synthesized at the nanoscale by the co-precipitation method via a sonochemical approach. High-intensity ultrasonic radiation treated the hydroxide suspension at 90 °C for 2 hours. Both the X-ray diffraction analysis (XRD) and the Fourier transform infrared spectra (FT-IR) analysis confirm the presence of the cubic spinel phase with a grain size of 15 – 25 nm. The vapor adsorption experiments confirmed that the pore surface area was found to be 95.34 m2/g by N2 adsorption desorption isotherm, and the material was mesoporous. The saturation magnetization of ferrite powders was investigated using a vibrating sample magnetometer (VSM). This work mainly focuses on the removal of Malachite green (MaG) and Methyl green (MG) with the help of adsorption technology from water using Ni0.5Zn0.5Fe2O4 spinel ferrites. The adsorption studies examined the impact of mass and pH, revealing that both factors influence adsorption. The optimum conditions for Malachite green and Methyl green adsorption onto the spinel Ni-Zn ferrites were 0.02 g for spinel mass, pH values (6−8). At 328 K, the maximum capacity for Ni0.5Zn0.5Fe2O4 spinel adsorbents was 82 and 180 mg/g MaG and MG, respectively. The removal efficiency for MaG and MG dye was respectively 95 % in 420 and 180 minutes. According to the kinetic studies, a pseudo-second-order model is the most suitable model for the adsorption process. The adsorption mechanism was examined by fitting the adsorption data to Langmuir, Freundlich, Radushkevich, and Temkin adsorption models. The Langmuir model can adequately describe results.

Enhancing dye/salt separation efficiency through polysulfobetaine-modified poly (triazine imide)/polyethersulfone (PTI-PSBMA/PES) composite membrane fabrication

Membrane technology stands as a vital solution for efficient dye/salt separation in various industrial processes. For the first time in this study, polysulfobetaine-modified poly (triazine imide) (PTI-PSBMA) was simply prepared by reversible addition-fragmentation chain-transfer (RAFT) polymerization as an additive for PTI-PSBMA/PES composite membrane preparation using the phase inversion strategy. The SEM, AFM pictures, and WCA analysis results exhibited that the modified membranes with PTI-PSBMA possess smoother surfaces and are more hydrophilic. After conducting an investigation using a dead-end filtration setup, it has been determined that the PTIZ-1 membrane, containing 1.0 wt% of PTI-PSBMA, emerged as the most effective membrane. This membrane exhibited a remarkable water flux of 46.0 L. m−2 h−1 bar−1 and demonstrated the highest rejections for various dyes, such as Reactive Red 120 (92.3 %), Direct Yellow 29 (79.3 %), and Methyl Green (85.0 %). Additionally, the PTIZ-1 membrane displayed impressive antifouling properties, with protein adsorption decreasing by over 96.0 %. With exceptional rejection rates for dyes and high permeability for salts, this composite membrane presents a promising solution for practical applications in wastewater treatment and dye removal processes. This research contributes to advancing membrane technology by introducing a highly efficient composite membrane with enhanced separation properties, addressing critical challenges in industrial dye/salt separation processes.

An Electrochemical DNA Sensor for Doxorubicin Based on Graphene Oxide, Electropolymerized Azure A, and Methylene Green Composites

An Electrochemical DNA Sensor for Doxorubicin Based on Graphene Oxide, Electropolymerized Azure A, and Methylene Green Composites

Redox kinetics of methylene green: Titanium trichloride as a novel photo redox agent

Redox kinetics of methylene green: Titanium trichloride as a novel photo redox agent

Nickel-doped magnetic carbon aerogel derived from xanthan gum: a competent catalyst for the degradation of single and binary dye-based water pollutants.

Toxic organic dyes (colorants) are one of the main causes of water pollution that releases destructive effluents in the environment. To overcome this issue, a fundamental need to produce a novel, efficient catalyst for the degradation and mineralization of dye mixtures has arisen. The objective of this research is to develop an eminent Ni-doped magnetic carbon aerogel (Ni-MCA) catalyst using graft co-polymerization method having xanthan gum as backbone doped with Ni-magnetic nanoparticles (Ni-MNPs), that do not show agglomeration and easy to separate. The examination revealed that Ni-MCA provided exceptional magnetic characteristics (Ms = 52.75emu/g) and potent catalytic activity for the degradation of mono- as well as binary-dye solutions of Congo red (CR) and methyl green (MG) dyes. The formation was verified by various characterization techniques such as FTIR, VSM, XRD, XPS, SEM, TEM, and EDX mapping. Interestingly, Ni-MCA shows faster result on anionic dye CR up to 97% with degradation rate of 5.647 × 10-1min-1, and MG dye shows degradation of 95.7% with the degradation rate of 2.169 × 10-1min-1, while dye mixture is showing 90% degradation with rate of 2.159 × 10-1min-1.

In situ polymerization of acrylamide on magnetic SnFe2O4/CeO2 nanocomposite: A novel adsorbent for removing various dyes

Environmental conservation requires effective, secure, and economical treatment options for dye-contaminated wastewater. The current study comprises a novel fabrication of tin ferrite/ceria/polyacrylamide magnetic and porous ternary nanocomposite. This occurs through crosslinking polymerization of acrylamide on the SnFe2O4/CeO2 binary nanocomposite. The SnFe2O4/CeO2/PAM nanocomposite was comprehensively characterized using FTIR, TGA, XRD, TEM, VSM, EDX, SEM and N2 adsorption-desorption isotherms. The ternary nanocomposite's efficiency as a novel adsorbent for anionic (direct violet 4, DV4) and cationic (bismarck brown r, BBR) azo dyes was investigated. A range of variables were studied to optimize the effectiveness of eliminating both dyes. In an acidic medium, DV4 removal was more efficient, whereas BBR removal was higher in an alkaline environment. Non-linear regression was employed to analyze adsorption kinetics and isotherm models, using three statistical error functions to determine the best-fit models. Adsorption data for both dyes demonstrated a good conformity with pseudo-second-order and Freundlich isotherm models. The dyes' adsorption was both endothermic and spontaneous. The nanocomposite displayed notable performance throughout five reuses. Moreover, the nanocomposite shows good adsorption efficiency for various dyes (congo red, acid blue 40, methyl green, and crystal violet) as well as DV4 and BBR. Therefore, it emerges as a promising adsorbent for wastewater purification.