Methylene Blue Degradation Efficiency Research Articles

Facile construction of Bi2WO6/TiO2 microspheres heterojunction for boosting photocatalytic degradation of organic dyes

Flower-like Bi2WO6 microspheres and TiO2 spherical particles were prepared by a facile hydrothermal method without any surfactant or template. A unique Z-Scheme Bi2WO6/TiO2 heterojunction was successfully synthesized via a simple physical mixing method. The effect of mass ratio on the structure, morphology, optical properties, BET surface area and photocatalytic performance evaluated by degradation of organic dyes including Rhodamine B (RhB), methylene blue (MB) and methyl orange (MO) under solar irradiation was systemically investigated. When the mass ratio of Bi2WO6 to TiO2 was 1:4, the Bi2WO6/TiO2 composites exhibited the highest photocatalytic degradation efficiency, the highest degradation efficiency of RhB and MB reached 95.2 % and 89.3 %, which could be attributed to the construction of heterojunction structure between TiO2 and Bi2WO6. The optical absorption capacity of Bi2WO6/TiO2 composites was stronger than pure TiO2. Furthermore, the radical-quenching experiments proved that ·O2– and h+ played crucial roles in the photocatalytic reaction. The suitable band potential of Bi2WO6 (3.19 eV) and TiO2 (2.89 eV) revealed the Z-Scheme pathway and possible photocatalytic mechanism of Bi2WO6/TiO2 composites for organic dyes degradation. Thus, the direct Z-scheme Bi2WO6/TiO2 heterojunction effectively promoted separation of photogenerated electron-hole pairs, resulting in higher photocatalytic activity.

Bimetal Cu/Ni-BTC@SiO2 metal-organic framework as high performance photocatalyst for degradation of azo dyes under visible light irradiation

There has been significant attention on the efficient degradation of pollutants in wastewater using metal-organic frameworks (MOFs) photocatalytic methods over the past decade. Herein, we examined the elimination of two different types of water-contaminating dyes, specifically cationic dye methylene blue (MB) and anionic dye methyl orange (MO), through the application of bimetal Cu/Ni-BTC@SiO2 MOF as high performance photocatalyst. The bimetal Cu/Ni-BTC@SiO2 photocatalyst was synthesized and characterized by XRD, FTIR, SEM, TEM, TGA, BET, DRS, and VSM techniques. The examination of the impact of different operational factors on the elimination of pollutants involved a comprehensive analysis of variables including the photocatalyst type, initial pollutant concentration, quantity of photocatalyst, and pH levels. The highest removal efficiency for MO and MB dyes by the photocatalyst was found to be 98 and 71%, respectively, within 60 min. In the fifth reaction stage, degradation efficiency for MO and MB was 76 and 56% respectively. Kinetic investigations demonstrated that, in the context of the uptake of MB and MO dyes, the interparticle diffusion, and pseudo-second-order models emerged as possessing the most robust correlation coefficients with the experimental data, registering values of 0.988 and 0.961, respectively. The examination of isotherms reveals that the isotherm models proposed by BET, and Anderson (V) demonstrate the highest level of conformity with the empirical data for the decomposition of MB and MO dyes, correspondingly. The TOC levels decreased significantly from 51 to 14 and 47 to 3 mg/L for MB and MO dyes, indicating the effective mineralization process using Cu/Ni-BTC@SiO2.

Preparation of modified wood-based metal nanoparticles synthesized in situ and efficient removal of organic pollutants from wastewater

Wood has excellent properties such as biodegradability, high reactivity and rich channel skeleton structure. However, the defects such as hole blockage and limited specific surface area limit the application of wood-based materials in wastewater treatment. Therefore, in this research, wood substrates (DTWS) were treated using a deep eutectic solvent method, which was able to remove both lignin and hemicellulose from wood. Wood-based carriers with high specific surface area and high chemical activity were formed. The DTWS-Ag material was formed by growing Ag nanoparticles (NPs) in wood channels by hydrothermal method. The results showed that with the increase of lignin and hemicellulose removal, the degradation performance of DTWS-Ag material showed a volcanic trend due to the interaction between Ag and the inner wall of the pipe. The pore size and the amount of Ag NPs are very important to the degradation rate of dye molecules. DTWS-4-Ag composite material makes wood pore diameter and Ag NPs production reach a high balance, so that it has the highest degree of reduction. DTWS-4-Ag showed high catalytic degradation efficiency and stability for methylene blue degradation, with the degradation efficiency up to 98.3%. This low-cost, renewable wood-based filter has high dye degradation efficiency and can be widely used in practical wastewater treatment.

Modeling and experimental verification for photodegradation in a spinning disk reactor

The spinning disk reactor has been regarded as a process intensification device in photochemical processes, which decreases the light path length by the thin film formation created by centrifugal force. A reliable reactor model was indispensable for the practical application of photoreactors. Our previous studies proposed a spinning disk reactor with elliptic-cylindrical and cylindrical spoilers for photochemical process intensification, and then hydrodynamic parameters of liquid film thickness, photon absorption rate, and residence time distribution were obtained. Based on the obtained parameters, herein, a reactor model was further established for the description of photodegradation reaction in the innovative spinning disk reactor. Different non-ideal flow models were employed during the model development, including the tanks-in-series model and axial dispersion model. The apparent reaction rate constant of a spinning disk reactor with spoilers was determined by the photon absorption rate, which was in the range of 0.088–0.268 s−1. The reactor model was verified by the experiments on photodegradation of Methylene Blue under different disk configurations and operating conditions. The degradation efficiency of Methylene Blue could reach up to 89.8 % in 25 min at N = 200 r/min, Q = 60 L/h, and I0 = 8 mW/cm2. The deviation between predicted and experimental Methylene Blue degradation efficiencies was within ± 20 %, confirming the rationality of the reactor model. The developed model lays the foundation for the scaling-up and commercial applications of the novel spinning disk reactors.

TiO2-N/Polystyrene photocatalyst-combined Corona Plasma Treatment for Methylene Blue Degradation

<span>This study employed the corona plasma method combined with TiO<sub>2</sub>-N/PS photocatalyst to degrade dye pollutants. The plasma reactor consisted of two needle-shaped stainless steel electrodes connected to a voltage of 8 kV. Methylene blue (MB) solution was used as a model pollutant with varied initial concentrations of 10, 50, and 100 ppm. The degradation efficiency was evaluated based on the absorbance of the degraded MB solution measured using a UV-Vis spectrophotometer. The results exhibited that the longer plasma treatment duration caused the absorbance value of the degraded MB to decrease, and then the MB degradation efficiency increased. MB-10 demonstrated a maximum degradation efficiency of 99.40% after plasma treatment for 30 minutes. Meanwhile, MB-50 and MB-100 reached maximum degradation efficiencies of 95.29 and 86.55% efficiency after plasma treatment for 60 minutes. The greater initial MB concentration caused the longer degradation process. Furthermore, the results revealed no increase in degradation efficiency due to the addition of TiO<sub>2</sub>-N/PS photocatalyst into the plasma treatment. The degradation efficiencies of MB-10, MB-50, and MB-100 under TiO<sub>2</sub>-N/PS-combined plasma treatment for 30 min were 94.48, 81.57, and 5.22%, respectively. This suggests the possibility that the UV light generated during the plasma process cannot activate the TiO<sub>2</sub>-N/PS photocatalyst.</span>

Improving Photocatalytic Performance through Incorporation of Various Cations in A-site of Double Perovskite Material (Cs0.50MA0.50)2SnI6 for Degradation of Methylene Blue Dye Pollutant under Visible Light Irradiation

In this article, undoped double perovskite materials like caesium tin iodide (Cs2SnI6), methyl ammonium tin iodide [MA2SnI6: MA denotes CH3NH3+] and mixed double perovskite material [(Cs0.50MA0.50)2SnI6] were synthesized using a wet chemical methodology. The crystal structure confirmation, optical properties, thermal properties, surface morphology and presence of elemental composition of the prepared samples using XRD, UV, TGA and FESEM-EDAX analyses were thoroughly investigated. The synthesized materials were employed as photocatalysts to degrade methylene blue dye within 120 min under visible light. An increase in the optical properties of the synthesized double perovskite materials was confirmed by ultraviolet (UV) analysis, which showed that the introduction of various cations into the perovskite material at the A-site shifted the photoluminescence (PL) emission peak to the red. TGA results demonstrated that (Cs0.50MA0.50)2SnI6 has greater thermal stability, which was confirmed by the presence of 43% of sample despite the temperature reaching almost 870 ºC. Doped double perovskite material (Cs0.50MA0.50)2SnI6 exhibited increased photocatalytic activity, with methylene blue dye degradation efficiency attaining 89% after 120 min of visible light irradiation, which is greater than pure double perovskite materials. The photocatalytic degradation of methylene blue dye is mostly facilitated by hydroxyl radicals and holes, according to a radical trapping experiment that we conducted by employing different scavengers. The results of the current work showed that doped double perovskite materials [(Cs0.50MA0.50)2SnI6] exhibit high thermal stability as well as higher photocatalytic activity than pure double perovskite materials. A possible photocatalytic reaction process is also diagrammatically using the band positions of double perovskite materials found using Mott-Schottky plots , which confirms that the synthesized double perovskite material has an N-type semiconductor nature.

Carbon based cobalt titanate perovskite nanocomposite: Synthesis, characterization, and excellent visible light driven photocatalytic performance

Titanium-based perovskite oxides are the promising photocatalysts for an efficient degradation of organic pollutants. However, charge carriers recombination and wide band gap energy are still the main challenges in their visible-light-driven photocatalytic applications of Titanate perovskites, ATiO3. The immobilization of Titanium-based perovskites on a carbonaceous substrate such as nitrogen-rich carbon nitride, can be considered as an excellent option for enhancing photocatalytic performance. Here, the CoTiO3/C3N5 nanocomposite was synthesized by simple reflux method and used for photocatalytic degradation of three organic pollutants including methylene blue (MB), tetracycline hydrochloride (TC), and bisphenol A (BPA). The results indicated that the photocatalytic activity of the CoTiO3 perovskite was considerably improved by introducing C3N5 nanosheets and fabricating CoTP/C3N5 nanocomposite. The crystalline structure of CoTiO3/C3N5 (CoTP/C3N5) nanocomposites was confirmed successfully by XRD analysis. The specific surface area of the synthesized CoTP/C3N5 nanocomposite was 8.15 m2/g calculated by N2 adsorption–desorption technology. In the 60th minute of the photocatalytic process, the degradation efficiency of MB, TC, and BPA by CoTP/C3N5 were obtained as 98.70, 60.33, and 92.90 %, respectively, which were higher than pristine CoTiO3 nanorods and C3N5 nanosheets. Electrochemical impedance analysis shows that the CoTP/C3N5 nanocomposite has good electrochemical performance. The improvement photocatalytic activity CoTP/C3N5 can be attributed to the suppressing the recombination of photogenerated electrons and holes and good electrochemical performance with high electron transfer capability. The results achieved from UV–Visible Diffused Reflectance Spectroscopy (DRS), mott-schottky measurements and the photocatalytic degradation experiments in the presence of scavengers confirmed the significantly accelerating the Z-scheme charge transfer mechanism where photoexcited carriers can migrate between CoTiO3 perovskite and C3N5 nanosheets.

Effective degradation of synthetic micropollutants and real textile wastewater via a visible light-activated persulfate system using novel spinach leaf-derived biochar

A novel biochar (BC), derived from spinach leaves, was utilized as an activator for persulfate (PS) in the degradation of methylene blue (MB) dye under visible light conditions. Thorough analyses were conducted to characterize the physical and chemical properties of the biochar. The (BC + light)/PS system exhibited superior MB degradation efficiency at 83.36%, surpassing the performance of (BC + light)/hydrogen peroxide and (BC + light)/peroxymonosulfate systems. The optimal conditions were ascertained through the implementation of response surface methodology. Moreover, the (BC + light)/PS system demonstrated notable degradation ratios of 90.82%, 81.88%, and 84.82% for bromothymol blue dye, paracetamol, and chlorpyrifos, respectively, under optimal conditions. The predominant reactive species responsible for MB degradation were identified as sulfate radicals. Notably, the proposed system consistently achieved high removal efficiencies of 99.02%, 96.97%, 94.94%, 92%, and 90.35% for MB in five consecutive runs. The applicability of the suggested system was further validated through its effectiveness in treating real textile wastewater, exhibiting a substantial MB removal efficiency of 98.31% and dissolved organic carbon mineralization of 87.49%.

In-situ one-pot synthesis, characterization of magnetic hydrochar and its application as Fenton-like catalyst for the degradation of methylene blue dye

The widespread use of dyes in various industries has led to alarming levels of water pollution, posing significant environmental and health risks. This study presents biochar being a carbon-rich source, produced from Acacia koa pod covers has been used as a sustainable source to prepare Ak/BC-Fe3O4 magnetic nanocomposite, subsequently employed for Fenton-like degradation of methylene blue (MB) dye. FESEM-EDS revealed that the synthesized nanocomposite has a morphology of spherical magnetic nanoparticles being embedded on the biochar base and EDS further confirmed the synthesis of magnetic biochar by detecting only C, O, and Fe. The nanocomposite is mesoporous with a pore volume of 0.03204 cm3/g and a surface area of 7.11 m2/g as shown by the BET results. XRD substantiated the presence of an amorphous structure of biochar and the presence of ultra-small crystallites of Fe3O4 nanoparticles. FTIR signified the presence of specific functional groups for Fe–O and biochar whereas, XPS showed the peaks at 712.39 and 725.78 eV indicated the coexistence of Fe2+ and Fe3+. The nanocomposite is superparamagnetic with a saturation magnetization of 8.64 emu/g having remarkable magnetic separation capacity. Fenton-like degradation of MB dye in the presence of H2O2 revealed a first-order reaction with removal efficiency ranging between 82 and 96% in 120 min with convenient recycling ability for 7 cycles. Hence, this study underscores the outstanding characteristics and MB degradation efficiency of Ak/BC–Fe3O4, emphasizing its synthesis from sustainable plant biomass as a promising solution to address water pollution challenges associated with dye contamination.

Facile one-step preparation of Co2CrO4 spinel from heterometallic compounds – Structural, magnetic, electrical and photocatalytic studies

Two isostructural heterometallic complex salts with mononuclear units, [NH(CH3)2(C2H5)][Cr(terpy)2][CoCl4]2 (1) and [NH(CH3)(C2H5)2][Cr(terpy)2][CoCl4]2 (2), were synthesized using a building block approach and characterized by single-crystal and powder X-ray diffraction (XRD), impedance spectroscopy and magnetization measurements. They exhibit particular humidity-sensing properties and very high proton conductivity at room temperature. The magnetization of complexes shows the high spin state of 3/2 for tetrahedrally coordinated CoII ions, which on cooling remain in the paramagnetic state within the CrIII network, which is antiferromagnetically correlated. The prepared compounds were thoroughly explored as single-source precursors for the formation of the spinel oxide Co2CrO4 by their thermal decomposition. By optimizing the annealing temperature, heating/cooling rates and holding times, the phase composition of thermal processing of 1 or 2 was evaluated: phase pure spinel Co2CrO4 was obtained by thermal treatment already at 450 °C. The structure, morphology, and optical properties of spinel oxides prepared at different temperatures were characterized using powder XRD, field emission scanning electron microscopy (SEM) and UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS), while electrical and magnetic by impedance spectroscopy and magnetization measurements. The determined band gap energy and nanosized crystallites prompted us to investigate the photocatalytic activity of spinel oxide produced at 450 °C in the degradation of dyes Rhodamine B (RhB) and Methylene blue (MB) under Vis irradiation without and with assistance of hydrogen peroxide (H2O2). The results show that the Co2CrO4/H2O2 system exhibits a significantly higher photoactivity response; the degradation efficiency of MB and RhB was found to be 86.1% and 80.3%, respectively. The electrical conductivity spectra and the activation energy for the DC conductivity demonstrate the electronically semiconducting behaviour of the Co2CrO4 oxide. The Co2CrO4 spinel has a ferrimagnetic ground state, with mixed CoII and CoIII ions on the tetrahedral and octahedral sites: CoII having a high spin state on both sites and CoIII having a high spin state on the tetrahedral site and a low spin state on the octahedral site. Different thermal treatments affect the magnetization according to the different sizes of the obtained crystallites.

Growth of CuS nanowire on copper mesh for efficient solar-driven water evaporation and wastewater purification

This study proposed a multifunctional material, CuS nanowire, grown on a copper mesh (CM), for application in wastewater purification. CuS/CM could rapidly evaporate and collect water under solar irradiation. CuS nanowires were successfully synthesized on CM through a liquid–solid reaction at room temperature, followed by sulfidation. Water evaporation experiments conducted using meshes suspended in water to determine the most efficient configuration revealed that CuS/CM was the most efficient material. Owing to the localized surface plasmon resonance induced by oxygen vacancies, CuS/CM exhibited a high water evaporation rate (4.0523 kg·m-2h−1 @ 3 sun) and energy conversion efficiency (96.1 %) in Structure A with a vertical length of 4 cm under 3 sun irradiation. To evaluate its effectiveness in wastewater treatment, CuS/CM was used to evaporate and collect methylene blue (MB)-contaminated water at rates of 1.5747 and 0.8624 kg·m-2h−1. Furthermore, CuS/CM demonstrated photocatalytic activity during MB degradation. Under xenon lamp illumination for 6 h, CuS/CM exhibited a 73 % degradation efficiency for MB, indicating its photocatalytic properties. CuS/CM effectively purify dyeing wastewater due to their fast water evaporation rate and the photocatalytic capability of CuS, making them promising for wastewater treatment and desalination applications.

Carbide lime as substrates to boost energy recuperation and dyestuff removal in constructed wetland-microbial fuel cell integrated with copper oxide/carbon cloth cathode.

Methylene blue (MB) was regarded as a highly toxic and hazardous substance owing to its irreparable hazard and deplorable damage on the ecosystem and the human body. The treatment of this colorant wastewater appeared to be one of the towering challenges in wastewater treatment. In this study, a microbial fuel cell coupled with constructed wetland (CW-MFC) with effective MB elimination and its energy recuperation concurrently based on the incorporation of carbide lime as a substrate in a new copper oxide-loaded on carbon cloth (CuO/CC) cathode system was studied. The crucial influencing parameters were also delved, and the MB degradation and chemical oxygen demand (COD) removal efficiencies were correspondingly incremented by 97.3% and 89.1% with maximum power output up to 74.1 mW m-2 at optimal conditions (0.2 g L-1 carbide lime loading and 500 Ω external resistance). The carbide lime with high calcium ion content was greatly conducive for the enrichment of critical microorganism and metabolic activities. The relative abundances of functional bacteria including Proteobacteria and Actinobacteriota were vividly increased. Moreover, the impressive results obtained in printed ink wastewater treatment with a COD removal efficiency of 81.3% and a maximum power density of 58.2 mW m-2, which showcased the potential application of CW-MFC.

Phyto-synthesis of tin oxide nanoparticles using Diospyros mollis leaves extract doped graphitic carbon nitride for photocatalytic methylene blue degradation and hydrogen peroxide production

In this study, tin oxide nanoparticles (SnO2 NPs) were combined with graphitic carbon nitride (gCN) to produce the SnO2/gCN composite for photocatalytic methylene blue (MB) degradation and H2O2 production. Specifically, SnO2 NPs were initially prepared using a biological pathway from Diospyros mollis leaves extract, followed by the incorporation on gCN via calcination treatment. Characterization of SnO2/gCN was conducted through analytical methods, including scanning electron microscopy, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, N2 sorption isotherm, photoluminescence spectroscopy, and ultraviolet-visible diffuse reflectance spectroscopy (UV-DRS). The optical band gap of the nanocomposite was also evaluated to be 2.44 eV using the Tauc plot and UV-DRS, which is lower than pristine gCN. The photocatalytic performance over the optimal 1.0SnO2/gCN sample was resultingly investigated, reaching over 99.76 % of MB degradation efficiency within 120 min, and 4060.78 μM/g.h of H2O2 production rate under visible light radiation. Insights into the mechanism revealed the vital participation of reactive radicals, especially •O2− and •OH, in the degradation of MB molecules, while the reusability of 1.0SnO2/gCN was also maintained after 4 succeeding photocatalytic cycles. Such findings affirm the promising applicability of the constructed SnO2/gCN material in many industries, namely the environmental remediation and cleaner production sectors.

Preparation and utilization of Zn-La oxide nanocatalyst as a binary composite for photocatalytic degradation of methylene blue dye: Optimization through RSM-BBD

In this research, the photocatalytic degradation of methylene blue (MB) dye was explored by employing Zn-La (zinc-lanthanum) oxide nanocatalysts under UV irradiation. Preparation of Zn-La oxide nanocatalysts was executed utilizing the co-precipitation technique, and the surface and morphology of the fabricated nanocatalyst were examined via X-Ray diffraction analysis (XRD), Fourier-transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), Barrett-Joyner-Halenda (BJH), Field emission scanning electron microscopy (FESEM), Transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) methods. BET-BJH analysis demonstrated that the specific surface area of the Zn-La oxide nanocatalyst was 20.43 m2/g. Moreover, the response surface methodology (RSM) procedure was utilized to influence the operational factors i.e., catalyst amount, pH, H2O2 dose, and UV power. The quadratic model proposed via the RSM technique with a high R2 value of 0.89, demonstrates its reliability. Besides, the maximum percentage of MB dye removal reached 75.18% under optimal conditions, which include a catalyst amount of 12.05 mg, pH of 9, H2O2 dose of 0.44 mL, UV power of 23 W, and a reaction time of 45 min. Further, under the mentioned conditions, after 120 min, the MB degradation efficiency reached 98.8%. The kinetic study exhibited that the reaction rate constant was 0.0363 min−1. According to the outcomes, Zn-La oxides have a higher ability to remove MB. After 5 consecutive reuse rounds, the reduction in the yield of MB removal using Zn-La oxide nanocatalysts was 5.4%. This study demonstrates that the Zn-La oxide nanocatalyst can be promisingly utilized for the degradation of MB dye suspension solution.

Two-step growth of alumina nanoparticle decorated graphene oxide surfaces: Effect on photocatalytic activity

As water pollution is increasing due to industrialization, there is a high demand for easy-processing photocatalytic materials to clean wastewater. Here, the improvement in the photocatalytic dye degradation effect of graphene oxide (GO) surfaces, made of ultra-sonication assisted modified Hummer's method, is demonstrated with increasing alumina (Al2O3) concentration in the range of 4–30 wt. %. Scanning electron microscopy and x-ray diffraction results suggest a gradual increment in crystalline Al2O3 nanoparticles (NPs) by reducing GO, in good agreement with the first-principles calculations. Moreover, x-ray photoelectron spectroscopy reveals the appearance of oxygenated functional groups with increasing Al2O3 concentration, leading to the formation of defect-rich GO as demonstrated by Raman spectroscopy. Ultraviolet-visible spectroscopy further reflects a maximum reduction in the optical bandgap from 1.88 to 1.56 eV up to a concentration of 15 wt. % Al2O3. Interestingly, the methylene blue degradation efficiency of GO under ultraviolet irradiation is also found to be improved from 45% to 64% with 15 wt. % Al2O3, whereas the formation of Al2O3 NPs in the range of 100–300 nm with 30 wt. % Al2O3 is found to be detrimental for photocatalytic activity.

Fabrication of MoO3/rGO/Au composite for increased photocatalytic degradation of methylene blue

Water line purification and wastewater treatment have become challenging in the fast-growing industry, infrastructure, textile, manufacturing world, etc. with this challenge, photocatalysis has gained substantial attention as an environmentally friendly process on which researchers are working aggressively and, in this progress, two-dimensional (2D) are in focus because of their good photocatalytic ability. Therefore, in this study, we present the synthesis of one such ternary composite material comprising molybdenum trioxide nanorods (MoO3NR), reduced graphene oxide (rGO) and gold nanoparticles (AuNR), with a specific focus on its enhanced photocatalytic performance. The ternary composite is prepared via a combination of in situ hydrothermal and laser ablation methods allowing for precise control over the growth and integration of the constituent materials. The structural and morphological properties of the MoO3 nanorods, rGO and Au ternary material were systematically characterized using various techniques, including UV-vis spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The obtained results suggest the successful formation of a composite, revealing the presence of uniformly dispersed MoO3 nanorods on the rGO sheets and evenly distributed Au nanoparticles throughout the structure. Photocatalysis evaluations conducted to assess the material performance under visible light irradiation exhibited significantly enhanced methylene blue degradation efficiency of 85.91% in 90[Formula: see text]min in comparison with individual MoO3 nanorods and rGO counterparts. The improved efficiency can be attributed to the combined effects arising from the integration of MoO3 nanorods, rGO and Au nanoparticles, which facilitate efficient light absorption, charge separation and catalytic reactions, which in turn reduces electron–hole recombination and improve photocatalytic performance. Also, the tunable morphology and collective effects of MoO3 nanorods, rGO and Au offer new avenues for designing highly efficient and stable photocatalytic materials.

Zeolite-encapsulated copper(II) complexes with NNO-tridentate Schiff base ligands: catalytic activity for methylene blue (MB) degradation under near neutral conditions.

Three novel copper Schiff base complexes, L1Cu(OAc)-L3Cu(OAc), bearing NNO tridentate ligands were synthesized and successfully entrapped in zeolite. All free and encapsulated complexes were fully characterized through experiments combined with theoretical calculations, and were subsequently employed as catalysts to activate H2O2 for degradation of methylene blue (MB). The catalytic activity of free complexes was tunable by substitution effects. The complex L3Cu(OAc) displayed enhanced efficiency by adopting bulky and donor substitutions due to the lower oxidation states. However, the free complexes exhibited modified structural and catalytic properties upon encapsulation into the zeolite. The constraint from the zeolite holes and coordination geometry caused the alteration of electronic structures and subsequently modified the reactivity. This study revealed that upon encapsulation, the larger molecular dimension of L3Cu(OAc) resulted in additional distorted geometry, leading to higher catalytic efficiency for MB degradation with more blue shifts in the UV-Vis spectrum. There was high catalytic activity by LnCu(OAc)-Y compared to that of the free complex, and high recyclability under near neutral conditions. In addition, the catalytic efficiency of L3Cu(OAc)-Y was higher or equivalent compared to other catalysts. This work provides new complexes with NNO tridentate ligands encapsulated inside zeolite and explains the relationship between the modified structure and functionality.

Optimizing the photocatalytic performance of SnO2 nanoparticles for methylene blue removal with variation in calcination temperatures

In recent years, numerous studies have been conducted to combine tin oxide (SnO2) with various semiconductor materials to boost its photocatalytic efficiency for water waste treatment, with minimal emphasis placed on intensifying the intrinsic capabilities of pure SnO2. The primary objective of this study is to enhance the photocatalytic efficiency of pure SnO2 nanoparticles (NPs) by modifying their morphology, structural, and optical properties. The SnO2 NPs were synthesized using precipitation method, followed by a calcination process at varying temperatures (non-calcined, 300 °C, and 500 °C). The changes in properties of SnO2 NPs were investigated utilizing X-ray diffraction (XRD), scanning electron microscopy (SEM), particle size analysis (PSA), Brunauer-Emmett-Teller (BET), and ultraviolet-visible (UV-Vis) spectroscopy. The results indicated that elevating the calcination temperature up to 500 °C resulted in an increase in both the average crystallite size (up to 10.50 nm) and crystallinity (up to 85.28 %). However, the highest photocatalytic efficiency for methylene blue degradation of 84.78 % was obtained from the SnO2 NPs calcined at 300 °C sample exhibiting the largest surface area of 83.97 m2g-1. This study affirms that the specific surface area of SnO2 NPs is a critical factor in their efficacy for degrading dye-contaminated water waste.

Fabrication of Ag3PO4/N-doped TiO2 nanotubes heterojunction photocatalysts for visible-light-driven photocatalysis

As an environmentally friendly and energy-efficient technology, photocatalysis holds considerable potential for eliminating organic pollutants. In this study, novel visible-light-driven Ag3PO4-decorated nitrogen-doped TiO2 nanotubes (Ag3PO4/N-TNTs) photocatalysts with advanced properties of heterostructures were successfully synthesized and used to degrade methylene blue (MB) dye. The fabrication of Ag3PO4/N-TNTs photocatalysts involved a two-step electrochemical anodization to obtain TiO2 nanotubes (TNTs) and the wet impregnation of the amorphous tubular structure in NH3 solution, followed by calcination in air to obtain crystallized nitrogen-doped TiO2 nanotubes (N-TNTs). Finally, the decoration of the N-TNTs with Ag3PO4 nanoparticles was conducted to enhance visible-light reactivity. Various heterojunction photocatalysts were obtained by changing the concentration of NH3 (0.5–2.5 M) and the dosage of Ag3PO4 (0.25–1.5 wt%) in the composites. Results of ultraviolet–visible (UV–Vis) absorption, photocurrent transient, and electrochemical impedance spectroscopy measurement revealed that Ag3PO4/N-TNTs possessed a significant response in the visible-light range and good photoelectronic properties. The superior photocatalytic activity of the Ag3PO4/N-TNTs catalyst was achieved under the optimal conditions of N-doping using 2-M NH3 and Ag3PO4 deposition at a dosage of 0.75 wt%. Based on the degradation efficiency (DE) of MB, the optimal Ag3PO4/N-TNTs exhibited rate constants of 4.5 and 2 times higher than those of the pristine TNTs and N-TNTs, respectively. The high stability of Ag3PO4/N-TNTs was confirmed through four cycles of reutilization, with a small decay of only 5.3% in the DE of MB dye for each run of photocatalysis. The scavenger tests of generated reactive oxygen species revealed that ·OH and ·O2− were the primary contributors to photocatalytic performance. The synthesized Ag3PO4/N-TNTs heterostructure photocatalysts were proven to possess efficient separation of photogenerated charge carriers, high reactivity, and stability in the visible-light region.

Decolorization and mineralization of methylene blue by potassium permanganate

Methylene blue (MB)-permanganate redox reaction has been studied spectrophotometrically in absence and presence of cationic cetyltrimethylammonium bromide (CTAB). The UV–visible spectroscopy reveals the presence of intermediate reaction products (Azure B, Azure A, and thionine) during interaction confirming the real degradation of MB. The gas chromatography-mass spectrometry (GC-EIMS) was used to establish the formation of MB degradation products. The electron transfers lead to a rapid N-demethylation oxidative reaction to form colored intermediary compounds. The key factors ([MnO4−], [MB], [H2SO4], and temperature) that affect the degradation rate of MB solution are analyzed. The redox reaction proceeds through a complex formation between the MB and MnO4−. The position of absorption band of MB was shifted from 666 nm to 603 nm with increasing the reaction time. The degradation efficiency decreases drastically from 82.1 % to 41.8 % in presence of 1.0 mM H2SO4. The results show that the degradation rate in acidic solutions is lower than that in neutral reaction media. The MnO2 was not formed as the product with H2SO4. The degradation efficiency of MB decreases with increasing CTAB concentrations. Sub-micellar inhibitory role of CTAB indicates that the MnO4− interact with positive head group of CTAB, and inhibit the oxidation of MB.