Illuminating the Power of V2O5 Nanoparticles: Efficient Photocatalytic Degradation of Organic Dyes under Visible Light.

This research explores the synthesis, characterization, and application of Vanadium Pentoxide nanoparticles (V2O5 NPs), focusing on their efficacy in the photocatalytic degradation of organic dyes under visible light. Utilizing a co-precipitation method, we synthesized V2O5 NPs characterized by an orthorhombic crystal structure with a consistent average particle size of 28 nm. The optical properties of V2O5 NPs, including their band gap, were thoroughly investigated to understand their light absorption capabilities, which are crucial for photocatalytic activity. In our study, Methyl Violet (MV) dye was employed as a model organic pollutant to assess the photocatalytic performance of the nanoparticles. Under visible light irradiation, the V2O5 nanoparticles demonstrated an exceptional photocatalytic degradation efficiency, achieving up to 85% degradation of the MV dye within 100 min. This high level of efficiency is attributed to the nanoparticles' ability to effectively absorb visible light and generate electron-hole pairs, thereby facilitating a robust degradation process. Further analysis revealed that the photocatalytic activity led to the generation of reactive oxygen species (ROS) such as superoxide and hydroxyl radicals, which are integral to the dye degradation mechanism. These ROS play a critical role in breaking down the dye molecules, significantly contributing to the overall effectiveness of the photocatalytic process. The results of this study highlight the potential of V2O5 nanoparticles as a sustainable and effective photocatalytic material for environmental remediation applications, particularly in the treatment of wastewater containing organic dyes. This research not only advances our understanding of the photocatalytic properties of V2O5 nanoparticles but also demonstrates their practical application in addressing environmental pollution through innovative and efficient degradation of hazardous substances.

Food-grade algae modified Schiff base-chitosan benzaldehyde composite for cationic methyl violet 2B dye removal: RSM statistical parametric optimization.

This work aims to apply the use of food-grade algae (FGA) composited with chitosan-benzaldehyde Schiff base biopolymer (CHA-BD) as a new adsorbent (CHA-BA/FGA) for methyl violet 2B (MV 2B) dye removal from aqueous solutions. The effect of three processing variables, including CHA-BA/FGA dosage (0.02-0.1 g/100 mL), pH solution (4-10), and contact duration (10-120 min) on the removal of MV 2B was investigated using the Box-Behnken design (BBD) model. Kinetic and equilibrium dye adsorption profiles reveal that the uptake of MV 2B dye by CHA-BA/FGA is described by the pseudo-second kinetics and the Langmuir models. The thermodynamics of the adsorption process (ΔG°, ΔH°, and ΔS°) reveal spontaneous and favorable adsorption parameters of MV 2B dye onto the CHA-BA/FGA biocomposite at ambient conditions. The CHA-BA/FGA exhibited the maximum ability to absorb MV 2B of 126.51 mg/g (operating conditions: CHA-BA/FGA dose = 0.09 g/100 mL, solution pH = 8.68, and temperature = 25 °C). Various interactions, including H-bonding, electrostatic forces, π-π stacking, and n-π stacking provide an account of the hypothesized mechanism of MV 2B adsorption onto the surface of CHA-BA/FGA. This research reveals that CHA-BA/FGA with its unique biocomposite structure and favorable adsorption properties can be used to remove harmful cationic dyes from wastewater.

The first novel aspect of this research work comes from the utilization of food-grade algae which contains various types of negative functional groups hydroxyl, carboxyl, and phosphate to modify a cationic biopolymer (Chitosan) to improve its adsorptive property toward removal of a cationic dye such as methyl violet 2B. The second novel aspect of this research work is to use the hydrothermal process to assist the grafting of an aromatic ring of benzaldehyde into the polymer matrix of the chitosan-food grade algae composite via a Schiff base linkage to improve its chemical stability and functionality.

Fabrication of ZnCo2O4-Zn(OH)2 Microspheres on Carbon Cloth for Photocatalytic Decomposition of Tetracycline.

Zinc cobalt oxide-zinc hydroxide (ZnCo2O4-Zn(OH)2) microspheres were successfully fabricated on carbon cloth via a sample hydrothermal method. The surface morphology of these microspheres and their efficacy in degrading methyl violet were further modulated by varying the thermal annealing temperatures. Adjusting the thermal annealing temperatures was crucial for controlling the porosity of the ZnCo2O4-Zn(OH)2 microspheres, enhancing their photocatalytic performance. Various analytical techniques were utilized to evaluate the physical and chemical properties of the ZnCo2O4-Zn(OH)2 microspheres, including field-emission scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, field-emission transmission electron microscopy, X-ray photoelectron spectroscopy, and UV-vis spectroscopy. Compared to untreated ZnCo2O4-Zn(OH)2 microspheres, those subjected to thermal annealing exhibited increased specific surface area and light absorption capacity, rendering them highly effective photocatalysts under UVC light exposure. Subsequent studies have confirmed the superior performance of ZnCo2O4-Zn(OH)2 microspheres as a reusable photocatalyst for degrading methyl violet and tetracycline. Furthermore, trapping experiments during the photodegradation process using ZnCo2O4-Zn(OH)2 microspheres identified hydroxyl radicals (·OH) and superoxide radicals (·O2⁻) as the primary reactive species.

Synthesis and characterization of g-C3N4-modified zeolite and its application as a methyl violet 6b cationic dye sorbent.

This paper reports a novel, low-cost, and facile approach to prepare a hybrid material consisting of zeolite, Fe3O4, and graphitic carbon nitride as a sorbent to remove methyl violet 6b (MV) from aqueous solutions. To improve the performance of the zeolite for the removal of MV, graphitic carbon nitride (with different C-N bonds and conjugated π region) was used. Also, to perform an easy and fast separation of sorbent from aqueous media, magnetic nanoparticles were incorporated into the sorbent. The prepared sorbent was characterized by different analytical techniques such as X-ray diffraction analysis, Fourier transform infrared, field emission scanning electron microscopy, and energy-dispersive X-ray analysis. The effects of four parameters of initial pH, initial concentration of MV, contact time, and the adsorbent amount on the removal process were investigated and optimized by the central composite design method. The removal efficiency of MV was modeled as a function of the experimental parameters. Affording to the proposed model, the values of 10 mg, 28 mg L-1, and 2 min were selected as optimum condition for adsorbent amount, initial concentration, and contact time, respectively. Under this condition, the optimal removal efficiency was 86% ± 2.8 which were close to the predicted value of the model (89%). Therefore, the model could fit and predict the data. The maximal adsorption capacity of sorbent derived from Langmuir's isotherm was 384.6 mg g-1. The applied composite can efficiently remove MV from various wastewater samples (paint, textile industries, pesticide production wastewater samples, and municipal wastewater).

Synthesis of wheat bran sawdust/Fe3O4 composite for the removal of methylene blue and methyl violet.

Magnetically modified nanomaterials have recently gained a great attention in wastewater treatment. In this study, the uptake process of methylene blue (MB) and methyl violet (MV) from aqueous media using wheat bran sawdust/Fe3O4 composite was studied. To specify the surface and structural properties of the wheat bran sawdust/Fe3O4 composite, various analyses such as FTIR, XRD, EDX, Map, TGA/DTG, SEM, VSM, and BET were performed. The results of BET analysis indicated that the specific surface area of the aforementioned composite was 74.25 m2/g, and the average pore size was 65.7A, which indicates that the composite has a mesoporous structure. Also, VSM analysis indicated that the composite has a paramagnetic property with a magnetic saturation of 28.29 emu/g and can be easily eliminated from the aqueous solution by a magnet. Moreover, the highest removal efficiency of MB and MV dyes using the wheat bran/Fe3O4 composite was obtained as 97.46 and 98.75%, respectively, which were significant values. These removal efficiencies were obtained at contact time of 50 min and pH values of 9 and 8 for MB and MV, respectively. Furthermore, the outcomes of equilibrium study showed that the Langmuir model with a correlation coefficient greater than 0.98 describes the equilibrium behavior of the uptake process better than the Freundlich and Dubinin-Radushkevich models. Besides, the maximum sorption capacity of MV and MB dyes using the Langmuir model was obtained as 46.08 and 51.28 mg/g, respectively. Also, the uptake process followed the pseudo-second-order kinetic model, and the thermodynamic study indicated that the uptake process is exothermic and spontaneous.

Fast decolorization of cationic dyes by nano-scale zero valent iron immobilized in sycamore tree seed pod fibers: kinetics and modelling study.

In the present work, Sycamore (Platanus occidentalis) tree seed pod fibers (STSPF) and nano-scale zero valent iron particles (nZVI) immobilized in Sycamore tree seed pod fibers (nZVIʘSTSPF) were produced. This biosorbent has been utilized as a viable effective biosorbent in the removing of methylene blue hydrate (MB), malachite green oxalate(MG), methyl violet 2B(MV) dyes from synthetic wastewater. The biosorbents were characterized by scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) spectroscopy. Various parameters such as contact time, solution concentration, pH and amount of biosorbent were investigated in order to evaluate the potential of the nanomaterials immobilized on natural wastes as sorbing biomaterials for the cationic dyes. Study on sorption kinetic and the sorption isotherm was carried out and best fitting models for the rate kinetics and isotherms were suggested. Langmuir isotherm was observed to be compatible with the isotherm models. The STSPF in the raw form showed the best dye sorption capacity of 43.67 mg/g for MG, 25.32 mg/g for MV, and 126.60 mg/g for MB. The magnetic nZVIʘSTSPF showed the best dye sorption capacity 92.59 mg/g for MG, 92.59 mg/g for MV, and 140.80 mg/g for MB. The iron nanoparticles immobilized biosorbent exhibited a higher removal capacity for all dyes compared to the raw biosorbent.

Phytoextraction potential of water fern (Azolla pinnata) in the removal of a hazardous dye, methyl violet 2B: Artificial neural network modelling.

This study investigated the potential of Azolla pinnata (AP) in the removal of toxic methyl violet 2B (MV) dye wastewater using the phytoextraction approach with the inclusion of an Artificial Neural Network (ANN) modelling. Parameters examined included the effects of dye concentration, pH and plant dosage. The highest removal efficiency was 93% which was achieved at a plant dosage of 0.8 g (dye volume = 200 mL, initial pH = 6.0, initial dye concentration = 10 mg L-1). A significant decrease in relative frond number (RFN), a growth rate estimator, observed at a dye concentration of 20 mg L-1 MV indicated some toxicity, which coincided with the plant pigments studies where the chlorophyll a content was lower than the control. There were little differences in the plant pigment contents between the control and those in the presence of dye (5 to 15 mg L-1) indicating the tolerance of AP to MV at lower concentrations. A three-layer ANN model was optimized (6 neurons in the hidden layer) and successfully predicted the phytoextraction of MV (R = 0.9989, RMSE = 0.0098). In conclusion, AP proved to be a suitable plant that could be used for the phytoextraction of MV while the ANN modelling has shown to be a reliable method for the modelling of phytoextraction of MV using AP.

Sulfate radical induced degradation of Methyl Violet azo dye with CuFe layered doubled hydroxide as heterogeneous photoactivator of persulfate.

Persulfate (PS)-based advanced oxidation processes have aroused considerable attentions due to their higher efficiency and wider adaptability to the degradation of bio-recalcitrant organic contaminants. In this study, Cu-Fe layered doubled hydroxide (CuFe-LDH) was employed to degrade Methyl Violet (MV) through heterogeneous photo-activation of PS under visible-light irradiation. The reaction kinetics, degradation mechanism, catalyst stability were investigated in detail. Under the conditions of CuFe-LDH (3:1) dosage 0.2 g/L, PS concentration 0.2 g/L and without initial pH adjustment, 20 mg/L MV was almost completely degraded within 18 min. Electron Spin Resonance (ESR) test and radical quenching experiment indicated that sulfate radicals (SO4-) were the dominant reactive oxidants for the MV decolorization, while hydroxyl radicals (OH) were also involved. The CuFe-LDH/PS/Vis system was applicable at wide range of pH level (3-9). However, extreme pH level would lead to the reduction or transformation of SO4-. The catalyst CuFe-LDH exhibited excellent stability and maintained relatively high catalytic activity to PS even after four recycles. Mechanism study revealed that the redox cycle of Fe3+/Fe2+ and Cu2+/Cu3+ assisted by visible-light irradiation accounted for the enhanced generation of radicals in CuFe-LDH/PS/Vis system, resulting in the improved degradation of organic contaminants. Overall, the CuFe-LDH/PS/Vis process could be a promising approach for the removal of refractory organic pollutants in wastewater.

Microwave treated Salvadora oleoides as an eco-friendly biosorbent for the removal of toxic methyl violet dye from aqueous solution--A green approach.

In the present study, microwave treated Salvadora oleoides (MW-SO) has been investigated as a potential biosorbent for the removal of toxic methyl violet dye. A batch adsorption method was experimented for biosorptive removal of toxic methyl violet dye from the aqueous solution. The effect of various operating variables, viz., adsorbent dosage, pH, contact time and temperature on the removal of the dye was studied and it was found that nearly 99% removal of the dye was possible under optimum conditions. Kinetic study revealed that a pseudo-second-order mechanism was predominant and the overall process of the dye adsorption involved more than one step. Hence, in order to investigate the rate determining step, intra-particle diffusion model was applied. Adsorption equilibrium study was made by analyzing Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) adsorption isotherm models and the biosorption data was found to be best represented by the Langmuir model. The biosorption efficiency of MW-SO was also compared with unmodified material, Salvadora oleoides (SO). It was found that the sorption capacity (qmax) increased from 58.5 mg/g to 219.7 mg/g on MW treatment. Determination of thermodynamic parameters such as free energy change (ΔG°), enthalpy change (ΔH°) and entropy change (ΔS°) confirmed the spontaneous, endothermic and feasible nature of the adsorption process. The preparation of MW-SO did not require any additional chemical treatment and a high percentage removal of methyl violet dye was obtained in much lesser time. Thus, it is in agreement with the principles of green chemistry. The results of the present research work suggest that MW-SO can be used as an environmentally friendly and economical alternative biosorbent for the removal of methyl violet dye from aqueous solutions.

Ammonium sulfide-assisted hydrothermal activation of palygorskite for enhanced adsorption of methyl violet.

Herein, palygorskite (PAL) was activated via a simple hydrothermal process in the presence of ammonium sulfide, and the effects of activation on the microstructure, physico-chemical feature and adsorption behaviors of PAL were intensively investigated. The hydrothermal process evidently improved the dispersion of PAL crystal bundles, increased surface negative charges and built more active -Si-O(-) groups served as the new "adsorption sites". The adsorption property of the activated PAL for Methyl Violet (MV) was systematically investigated by optimizing the adsorption variables, including pH, ionic strength, contact time and initial MV concentration. The activated PAL exhibited a superior adsorption capability to the raw PAL for the removal of MV (from 156.05 to 218.11mg/g). The kinetics for MV adsorption followed pseudo second-order kinetic models, while the isotherm and thermodynamics results showed that the adsorption pattern well followed the Langmuir model. The structure analysis of PAL before and after adsorption demonstrated that electrostatic interaction and chemical association of -X-O(-) are the prominent driving forces for the adsorption process.

Determination of phosphate in food based on molybdenum yellow derivatization coupled with resonance Rayleigh scattering method.

This paper proposed a rapid, selective and sensitive molybdenum yellow derivatization coupled with Resonance Rayleigh scattering (MYD-RRS) method for detection of phosphate. Under the acidic condition, phosphate can be selectively transformed to Keggin type of phosphomolybdic acid (PMA, i.e., PMo12O403-) through molybdenum yellow derivatization reaction prior to RRS detection. The PMA can further react with cationic methyl violet (MV) to form larger PMA-MV ion association complexes, generating significant RRS signal. The concentration of phosphate was linearly related to the RRS signal in the range of 8-200 ng/mL, with the determining coefficient (R2) of 0.9973 and the detection limit of 4 ng/mL. The analytical procedure can be completed within 10 min and the RRS signal intensity can remain stable more than 4 h. The method showed good stability toward temperature and time, and good anti-interference capability. The method was applied to the determination of phosphate in real food samples with the recovery of 85-117% and RSD of 1-5.2%. With the advantages of rapidness, high sensitivity and good selectivity, the MYD-RRS method exhibits great potential to the determination of phosphate in food. It also provides an instructive strategy for detection of analytes with weak RRS signal.

Enhancing cationic dye removal via biocomposite formation between chitosan and food grade algae: Optimization of algae loading and adsorption parameters.

Herein, a natural material including chitosan (CTS) and algae (food-grade algae, FGA) was exploited to attain a bio-adsorbent (CTS/FGA) for enhanced methyl violet 2B dye removal. A study of the FGA loading into CTS matrix showed that the best mixing ratio between CTS and FGA to be used for the MV 2B removal was 50 %:50 % (CTS/FGA; 50:50 w/w). The present study employed the Box-Behnken design (RSM-BBD) to investigate the impact of three processing factors, namely CTS/FGA-(50:50) dose (0.02-0.1 g/100 mL), pH of solution (4-10), and contact time (5-15 min) on the decolorization rate of MV 2B dye. The results obtained from the equilibrium and kinetic experiments indicate that the adsorption of MV 2B dye on CTS/FGA-(50:50) follows the Langmuir and pseudo-second-order models, respectively. The CTS/FGA exhibits an adsorption capacity of 179.8 mg/g. The characterization of CTS/FGA-(50:50) involves the proposed mechanism of MV 2B adsorption, which primarily encompasses various interactions such as electrostatic forces, n-π stacking, and H-bonding. The present study demonstrates that CTS/FGA-(50:50) synthesized material exhibits a distinctive structure and excellent adsorption properties, thereby providing a viable option for the elimination of toxic cationic dyes from polluted water.

High removal of methylene blue and methyl violet dyes from aqueous solutions using efficient biomaterial byproduct.

Dyes are among the toxic contaminants that significantly impact water ecosystems. A biomaterial prepared from Zizyphus Spina-Christi seed (ZSCS) to remove methylene blue (MB) and methyl violet (MV) from an aqueous solution was investigated. Several techniques have been used, including FTIR, SEM, EDX, XPS, and TGA, to characterize the physical and chemical properties of ZSCS. The effect of various parameters such as pH, adsorbent dosage, contact time, temperature, and initial dye concentration on the adsorption process were studied. The ZSCS adsorbent showed efficient MB and MV dye adsorption with Langmuir adsorption capacity of 666.66 and 476.19 mg/g, respectively, at experimental condition [(pH = 6; time = 30 min; T = 45 °C, dye concentration: 500 mg/L, and adsorbent dose = 0.6 g/L for MB and 1 g/L for MV dye)]. Kinetic and isotherm models were applied to fit the experimental outcomes. The result showed that ZSCS showed an ultrafast absorption process with a high removal efficiency of MB and MV within 5 min indicating its effective adsorption properties. The Langmuir isotherm model was the most suitable model for describing the adsorption of MB and MV dyes on ZSCS. The pseudo-second-order model kinetic fits better to MB and MV adsorption onto ZSCS than other models, suggesting that the adsorption mechanism followed chemisorption. Our results could offer an efficient cost-effective approach for dye removal from wastewater.

Synergistic effect of adsorption and photo-catalysis on the removal of hazardous dyes using steam exploded banana fiber derived micro-cellulose.

The utilization of banana fiber derived from micro-cellulose (MC) was exploited as a supporting material for advanced oxidation process (AOP) on the degradation of methylene blue and methyl violet dyes in the presence of H2O2-UV in aqueous medium for the first time using green chemistry protocols. Additionally, it was also effectively utilized for the adsorption of methylene blue dye using addition of H2O2 in the presence of sunlight. The MC powder was fabricated using an acid alkali process from the pseudo-stem of a banana tree. The as-fabricated MC powder was systematically characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectrometer (EDX), and zero point charge (pHzpc). The AOP assisted degradation of dye molecules was monitored by using calorimetric techniques as a function of dye concentration and pH in a batch reactor. In a short period of time, the maximum degradation efficiency of 98 % of methylene blue was achieved using MC powder assisted H2O2 under UV irradiation at a minimum irradiation time of 120 min at pH 7.0 using dosage of 0.2 g/L. However, in the absence of UV light, the degradation efficiency of MC powder assisted H2O2 was only about 5-10 % without UV light irradiation. The dye removal was studied as a function of various operational parameters such as pH (3-11), catalyst dose (0.2-0.6 g/L), and initial dye concentration (100-400 mg/L). In the presence of H2O2-sunlight and 0.2 g/L of dosage at pH 7.0 at a minimum contact time of 120 min, MC fiber showed maximum adsorption capacities of 98% and 85% for 100 mg/L and 400 mg/L of methylene blue concentrations. According to the obtained data, the adsorption of methylene blue dye on MC follows the Freundlich isotherm model (R2 = 0.9886) and pseudo-first-order kinetic model (R2 = 0.9596) due to the higher regression coefficients. This process of dye degradation and adsorption process is a novel one and environmentally benign for an effective removal of hazardous dyes.

Enhancing methyl violet 2B pollutant removal from wastewater using Al-MOF encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge: Synthesis, characterization, DFT calculation, adsorption optimization via Box-Behnken Design.

In this research, aluminum metal-organic framework encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge (Al-MOF@PIC) was prepared. SEM, FTIR, XPS, XRD, and BET techniques were employed to thoroughly characterize the synthesized material and establish its structure and characteristics. The study discovered that the Al-MOF@PIC is an efficient way to remove dyes, which constitute a significant number of contaminants in industrial wastewater. Subsequently the adsorption of methyl violet 2B (MV-2B) dye, the surface area, pore size, and pore volume of the adsorbent decreased from 1860.68 m2/g, 1.62 nm, and 1.52 cc/g to 1426.45 m2/g, 1.11 nm, and 0.92 cc/g, individually. This modification suggested that a portion of the MV-2B dye had been removed by adsorption over the adsorbent's pores. The excellent adsorption capacity of the material was further confirmed by batch adsorption tests, which displayed a maximum adsorption capability of 646.76 mg/g for the elimination of MV-2B dye. The high adsorption energy of 26.8 kJ/mol designates that chemisorption is primarily responsible for MV-2B dye adsorption against the sponge adsorbent. The Al-MOF@PIC composite sponge demonstrated exceptional reusability over six cycles, demonstrating its strength and durability. The Al-MOF@PIC composite sponge successfully removes MV-2B from water by pore filling, π-π stacking, hydrogen bonding, and electrostatic interactions, which are the key mechanisms behind the adsorption of the dye pollutant. Its potential for practical applications is further demonstrated using Box Behnken-design (BBD) to optimize the adsorption consequences.

Identification of methyl violet 2B as a novel blocker of focal adhesion kinase signaling pathway in cancer cells.

The focal adhesion kinase (FAK) signaling cascade in cancer cells was profoundly inhibited by methyl violet 2B identified with the structure-based virtual screening. Methyl violet 2B was shown to be a non-competitive inhibitor of full-length FAK enzyme vs. ATP. It turned out that methyl violet 2B possesses extremely high kinase selectivity in biochemical kinase profiling using a large panel of kinases. Anti-proliferative activity measurement against several different cancer cells and Western blot analysis showed that this substance is capable of suppressing significantly the proliferation of cancer cells and is able to strongly block FAK/AKT/MAPK signaling pathways in a dose dependent manner at low nanomolar concentration. Especially, phosphorylation of Tyr925-FAK that is required for full activation of FAK was nearly completely suppressed even with 1nM of methyl violet 2B in A375P cancer cells. To the best of our knowledge, it has never been reported that methyl violet possesses anti-cancer effects. Moreover, methyl violet 2B significantly inhibited FER kinase phosphorylation that activates FAK in cell. In addition, methyl violet 2B was found to induce cell apoptosis and to exhibit strong inhibitory effects on the focal adhesion, invasion, and migration of A375P cancer cells at low nanomolar concentrations. Taken together, these results show that methyl violet 2B is a novel, potent and selective blocker of FAK signaling cascade, which displays strong anti-proliferative activities against a variety of human cancer cells and suppresses adhesion/migration/invasion of tumor cells.

Polymeric Networks Derived from UV-Curing of Bio-Based Polyesters for Methyl Violet Removal.

In this study, firstly, the syntheses and characterizations of biobased polyesters with different acid values obtained from the condensation reaction of biobased itaconic acid and polyethylene glycol were investigated. Then, UV curing was applied to form polymeric networks as adsorbent material from these polyesters containing different acids. Fourier transform infrared spectrometry (FTIR), Nuclear Magnetic Resonance Spectroscopy (NMR), X-ray Photoelectron Spectroscopy (XPS), Gel Permeation Chromatography (GPC) and scanning electron microscope (SEM) were used for the characterization of polymeric networks. The effects of the parameters of contact time, initial dye concentration, pH, temperature, amount of adsorbent on adsorption were investigated by batch method. In addition, adsorption equilibrium data were analyzed by Langmuir, Freundlich, Tempkin, Elovich, Redlich-Peterson, Harkin-Jura and Jossens adsorption models. Kinetic and thermodynamic studies were performed at 298, 308, 318 and 328 K and desorption studies were also examined. Comparison studies for the effects of the acid values of the adsorbent materials on the removal of methyl violet (MV) organic pollutant from aqueous solutions were analyzed. According to the pseudo-second-order model, the adsorption capacities were found to be ≥ 357.14 mg/g for the adsorbents. From the thermodynamic data, it was determined that the mechanism was exothermic and spontaneous. As a result of the third reuse, it was found that the adsorbents had a removal efficiency of ≥ 72.36%. According to the results observed the increase in the acidities in the chemical structure of bio-based polymeric networks enhances the adsoption properties.

Adsorption of Cd (II) ions and methyl violet dye by using an agar-graphene oxide nano-biocomposite.

In this work, an agar-graphene oxide hydrogel was prepared to adsorb Cd (II) and Methyl Violet (MV) from water. The hydrogel was synthesised and characterised through SEM and EDS. Kinetic, equilibrium and regeneration studies were carried out, in which Langmuir, Freundlich and Sips isotherm models were fitted to the equilibrium experimental data; and regarding the kinetics, studies were conducted by modelling experimental data considering both empirical and phenomenological models. SEM and EDS have shown the composite present a 3D-disordered porous microstructure and that it is mainly constituted of C and O. Sips model fitted well to Cd (II) (R2 = 0.968 and χ2 = 0.176) and MV (R2 = 0.993 and χ2 = 0.783). The qmax values for MV and Cd (II) were 76.65 and 11.70 mg.g-1, respectively. Pseudo-order models satisfactorily described Cd (II) and MV adsorption kinetics with R2 > 0.90. Regeneration experiments revealed an outstanding reuse capacity of the adsorbent after three cycles of adsorption-desorption for both Cd (II) and MV. This study evidences the possibility of a feasible adsorbent for Cd (II) and MV removal from water for successive cycles of use.

The Biogenic Synthesis of Bimetallic Ag/ZnO Nanoparticles: A Multifunctional Approach for Methyl Violet Photocatalytic Degradation and the Assessment of Antibacterial, Antioxidant, and Cytotoxicity Properties.

In this study, bimetallic nanoparticles (NPs) of silver (Ag) and zinc oxide (ZnO) were synthesized using Leptadenia pyrotechnica leaf extract for the first time. Monometallic NPs were also obtained for comparison. The characterization of the prepared NPs was carried out using various techniques, including UV-Visible spectroscopy (UV-Vis), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The latter confirmed the crystalline nature and diameter of the monometallic and bimetallic NPs of Ag and ZnO. The SEM images of the prepared NPs revealed their different shapes. The biological activities of the NPs were evaluated concerning their antibacterial, antioxidant, and cytotoxic properties. The antibacterial activities were measured using the time-killing method. The results demonstrated that both the monometallic and bimetallic NPs inhibited the growth of Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria. The antioxidant activities of the NPs were evaluated using the DPPH (2,2-diphenyl-1-picrylhydrazyl) assay and their cytotoxicity was checked using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. The results indicated that the controlled quantity of the monometallic and bimetallic NPs did not affect the viability of the cells. However, the decreased cell (L-929) viability suggested that the NPs could have anticancer properties. Furthermore, the photocatalytic degradation of methyl violet and 4-nitrophenol was investigated using the prepared Ag/ZnO NPs, examining the factors affecting the degradation process and conducting a kinetic and thermodynamic study. The prepared Ag/ZnO NPs demonstrated good photocatalytic degradation (88.9%) of the methyl violet (rate constant of 0.0183 min-1) in comparison to 4-nitrophenol (NPh), with a degradation rate of 81.37% and 0.0172 min-1, respectively. Overall, the bimetallic NPs showed superior antibacterial, antioxidant, cytotoxic, and photocatalytic properties compared to the monometallic NPs of Ag and ZnO.

Removal Efficiency of Insoluble ß-Cyclodextrin Polymer from Water-Soluble Carcinogenic Direct Azo Dyes.

A batch system was applied to study the adsorption of three dyes (methyl violet, eriochrom black T and helianthin) from aqueous solution onto ß-cyclodextrin polymer, synthesized by using citric acid as a cross linking agent. This polymer lets to adsorb only methyl violet for this effect, several operator variables was checked only with this kind of dye, the removal efficiently increases with increase in adsorbent amount; elevation of temperature lets also to improve the dye adsorption; ionic strength has not effect on dye adsorption process, for the pH we have remarked a slight decrease in removal efficiently with increasing of pH values. Equilibrium study was investigated by applying three models (Langumir, Frendlich and Temkin), results show that Langumir isotherm is the appropriate model. FTIR spectra show the complex inclusion formation which dominates the adsorption mechanism, confirmed by the absence of characteristic peaks of methyl violet in ß-cyclodextrin after adsorption.