Methylene Blue Removal Efficiency Research Articles

NiTiO3 nanoparticles: An environmental game changer in electro-Fenton wastewater remediation

BackgroundIn the face of escalating water pollution challenges, the study explores the efficacy of Electro-Fenton (EF) treatment using NiTiO3 perovskite-modified cathodes for methylene blue (MB) removal from wastewater. MethodsEmploying a Central Composite Design (CCD) methodology, significant factors influencing the EF process, including initial MB concentration, pH, applied current, and reaction time, were optimized. The NiTiO3 catalyst was meticulously characterized, revealing its rhombohedral crystal structure, uniform particle distribution, and efficient charge transfer properties. FindingsElectrochemical analyses demonstrated the superior performance of the NiTiO3/Graphite electrode, emphasizing its increased electroactive sites, enhanced oxygen reduction capability, and reduced charge transfer resistance compared to the bare Graphite electrode. The EF process was finely tuned, demonstrating a 95.38 % removal efficiency of MB at optimal conditions (initial concentration: 25 mg L−1, pH: 4.5, current: 40 mA, time: 110 min). This study underscores the promising potential of NiTiO3-modified cathodes in advanced water treatment applications, highlighting their robust efficiency and environmental significance in combating persistent organic pollutants.

Engineering a staggered type-II Bi2WO6/WO3 heterojunction with improved photocatalytic activity in wastewater treatment

In recent years, the removal organic pollutants from wastewater by advanced oxidation processes, especially photocatalysis, has become a meaningful approach due to its eco-friendliness and low cost. Herein, staggered type-II Bi2WO6/WO3 heterojunction photocatalysts were prepared by a facile hydrothermal route and investigated by modern physicochemical methods (X-ray diffraction, scanning electron microscopy, low-temperature nitrogen adsorption-desorption, and diffuse reflectance spectroscopy). The optimized BWOW-5 photocatalyst exhibited a H2O2-assisted photocatalytic methylene blue removal efficiency of 94.1% (k = 0.01414 min−1) within 180 min under optimal reaction conditions, which is much higher than that of unmodified Bi2WO6 and WO3 due to efficient separation of the photogenerated charge carriers. The trapping experiments demonstrated that photogenerated hydroxyl radicals and holes play a key role in the photodegradation reaction. Moreover, the optimized BWOW-5 heterojunction photocatalyst exhibited excellent activity in the H2O2-assisted degradation of other pollutants, namely phenol, isoniazid, levofloxacin, and dibenzothiophene with the removal rate of 63.1, 73.6, 95.0, and 72.4%, respectively. This investigation offers a design strategy for Bi2WO6-based multifunctional photocatalytic composites with improved activity for organic pollutant degradation.

The Using of Plain PAC and PAC Impregnated with MgO and Fe2O3 as Catalysts for the Degradation of Cationic Dyes: Homogenous and Heterogeneous Ozonation

This study presented the removal of methylene blue in the batch system based on catalytic ozonation (heterogeneous and homogenous). The effect of variables such as initial MB (methylene blue)concentration, initial pH of solution (3-11), contact time (5-40 min), and catalyst dosage on homogeneous and heterogeneous ozonation systems was examined. The findings of the research showed that dye removal was better in alkaline conditions. The amount of dye removed in acidic conditions was slightly better than in neutral conditions (approximately 10% to 15%). In addition, the removal efficiency of dye was decreased by increasing of concentration. Besides, as the amount of catalyst (dosage) increased, the removal efficiency of MB had been increased by 40%. Due to the use of catalyst, the significant difference was between the use of two processes of single ozonation processes (SOP) and catalytic ozonation processes (COPs). The results indicated thatMB degradation in COPs was several times faster (approximately 4.7 times). It was due to the numerous advantages of these processes in the removal of environmental pollutants, they can be widely used in the removal of various pollutants if their cost can be reduced.

Polyaniline-supported g-C3N4/ZnO/Ag2CrO4 composite for photodegradation of methylene blue under visible light irradiation

Organic dyes are a major source of environmental pollution from different industries. To remove these recalcitrant, a novel ternary g-C3N4/ZnO/Ag2CrO4 and its polyaniline-supported (PANI) composites were synthesized using an “in situ” oxidative polymerization approach. XRD, SEM, UV–Vis DRS, and PL techniques were utilized to characterize the as-prepared composites. The photocatalytic efficiency was evaluated using a model organic pollutant, methylene blue (MB), and samples of the effluent of the textile industry. The as-synthesized ternary g-C3N4/ZnO/Ag2CrO4 (ZT3= 87.87 %) composite showed better photocatalytic performance than the single (5 %) and binaries (15–25 %) counterparts for MB degradation. The influence of various experimental settings on the photodegradation of MB dye was examined and these were an initial dye amount of 10 ppm, photocatalyst load of 0.15 g/L, and pH 10. Under optimized conditions, PANI-supported g-C3N4/ZnO/Ag2CrO4 composite (PAST) demonstrated substantial degradation efficiency (97.5 %). The reusability study of the spent catalyst revealed a reduced efficiency from 97.5 to 78.5 % photodegradation of MB after four successive cycles, demonstrating the photocatalyst's stability and efficiency. According to the study on the effect of scavengers, h+ plays a significant part in the discoloration of MB. The PAST photocatalyst outperformed the MB discoloration (97.5 %) and adequate degradation for real textile effluent samples (77.7 %) collected from Hawassa textile industries. The photodegradation efficiency result of this study demonstrated that PANI-supported g-C3N4/ZnO/Ag2CrO4 might serve as an advantageous photocatalyst for the efficient removal of MB and other dyes under visible light irradiation at the optimum conditions. The total estimated cost analysis of synthesis and photocatalytic degradation using Polyaniline-supported g-C3N4/ZnO/Ag2CrO4 composite found that it was quite affordable, costing around $5 per 1,000 L of wastewater treatment.

Zanthoxylum bungeanum Waste-Derived High-Nitrogen Self-Doped Porous Carbons as Efficient Adsorbents for Methylene Blue.

In this study, we prepared high-nitrogen self-doped porous carbons (NPC1 and NPC2) derived from the pruned branches and seeds of Zanthoxylum bungeanum using a simple one-step method. NPC1 and NPC2 exhibited elevated nitrogen contents of 3.56% and 4.22%, respectively, along with rich porous structures, high specific surface areas of 1492.9 and 1712.7 m2 g-1 and abundant surface groups. Notably, both NPC1 and NPC2 demonstrated remarkable adsorption abilities for the pollutant methylene blue (MB), with maximum monolayer adsorption capacities of 568.18 and 581.40 mg g-1, respectively. The adsorption kinetics followed the pseudo-second-order kinetics and the adsorption isotherms conformed to the Langmuir isotherm model. The adsorption mechanism primarily relied on the hierarchical pore structures of NPC1 and NPC2 and their diverse strong interactions with MB molecules. This study offers a new approach for the cost-effective design of nitrogen self-doped porous carbons, facilitating the efficient removal of MB from wastewater.

Gap type effect on photocatalytic degradation using newly hydrotalcite nanoposite precursor synthesized by hydrothermal method

<p>A novel technique involving hydrothermal synthesis was employed to prepare nanocomposite precursors of lamellar double hydroxide based basic mixed oxides. This method extended ongoing research on iron-impregnated hydrotalcite-supported nanomaterials. The iron-based Fe/MgAl-h nanocomposite was prepared via dry impregnation, introducing a known % by weight of Fe (NO3)3.9H2O metal salt into the hydrothermally synthesized MgAl-h structure. For comparative analysis, the photocatalytic performance of Fe/MgAl-h was compared with the coprecipitation-synthesized Fe/MgAl-c after calcination at 400°C, using various characterization techniques. Structural examination revealed a double-layered hydroxyl structure and the presence of iron oxide phase Fe2O3 in Fe/MgAl-h400. Optical assessments indicated an indirect band gap energy of 1.89 eV for solid Fe/MgAl-h400, which is suitable for visible light absorption. Photocatalytic experiments for methylene blue (MB) dye degradation in aqueous solution were performed under artificial irradiation with a tungsten lamp as the visible light source, mirroring the conditions of Fe/MgAl-c400. Using 50 mg/L MB concentration and 0.5 g/L catalyst quantity, increased MB removal efficiency with time was observed. A comparative study of hydrothermal and coprecipitation synthesis methods showed decreased photodegradation for the hydrothermally prepared solid. Fe/MgAl-h400 and Fe/MgAl-c400 exhibited reaction efficiencies of approximately 46% and 67%, respectively, possibly attributed to their distinct indirect and direct band gap characteristics. Moreover, a wider band gap in a semiconductor material offers several advantages for the degradation of dyes.</p>

Investigating the adsorption potential of char derived from waste latex for methylene blue removal

This study presents the adsorption of methylene blue (MB) dye using latex char derived from pyrolysis of latex gloves. The adsorption process was investigated systematically using Response Surface Methodology (RSM) with a Central Composite Design (CCD). The effects of four key variables, namely pH, time, temperature, and adsorbent dosage, were studied using a factorial design enriched with center points and axial points. Experimental data were analyzed using a second-order polynomial regression model to construct a response surface model, which elucidated the relationship between the variables and MB removal efficiency. The study found that the char obtained at 800 °C exhibited the highest adsorption capacity due to its increased carbonization, expanded surface area, and diverse pore structure. Analysis of Variance (ANOVA) confirmed the significance of the quadratic model, with remarkable agreement between predicted and experimental outcomes. Diagnostic plots validated the model's reliability, while 3D contour graphs illustrated the combined effects of variables on MB removal efficiency. Optimization using DoE software identified optimal conditions resulting in a 99% removal efficiency, which closely matched experimental results. Additionally, adsorption isotherms revealed that the Freundlich model best described the adsorption behavior, indicating heterogeneous surface adsorption with multilayer adsorption. This comprehensive study provides valuable insights into the adsorption process of MB dye using latex char, with implications for wastewater treatment and environmental remediation.

Optimized Bentonite Clay Adsorbents for Methylene Blue Removal

This study addresses the urgent need for effective water treatment methods by synthesizing and characterizing activated bentonite clay (ABC) adsorbents to remove methylene blue (MB) from aqueous solutions efficiently. Conventional adsorbents often exhibit limitations in efficiency and regeneration capabilities, necessitating novel approaches to water treatment. The primary objective is synthesizing and characterizing high-quality ABC adsorbents capable of effectively removing MB. The activation process was optimized, and adsorbent performance was evaluated regarding MB removal efficiency and regeneration potential. Various activation dos-ages were investigated, and comprehensive physicochemical characterization was performed using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), BET (Brunauer–Emmett–Teller) analysis, X-ray fluorescence (XRF), thermogravimetric analysis (TGA), and X-ray diffraction (XRD). The synthesized adsorbents demonstrated exceptional MB removal efficiency (99.593%) and impressive adsorption capacity (22.131 mg/g) when activated with 16 M sodium hydroxide. The adsorption process exhibited spontaneity and exothermicity, as validated by Freundlich and second-order kinetic models. Furthermore, the adsorbents showcased successful regeneration and reusability over three cycles, highlighting their potential for long-term application in water treatment. This study significantly advances water treatment by offering a novel approach to MB removal using base-activated bentonite clay (BABC) adsorbents, contributing to the development of sustainable water treatment solutions.

Synthesis of Novel Nanocomposite CaO/AC/ZnO from Biogenic Wastes of Date Palm Seeds from The Najran Region (Saudi Arabia) and Eggshells for Degradation of Methylene Blue

Metal nanoparticles and activated carbon-based nanocomposite materials are gaining popularity due to their numerous potential applications in a wide range of materials science areas. The current study aims to create novel photocatalyst frameworks for nanocomposites that were synthesized from biogenic waste and used to photodegrade methylene blue (MB) in wastewater under visible light. The activated carbon from date seeds was calcinated at a temperature of 700°C for two hours, and its surface was improved using zinc oxide nanoparticles and calcium oxide nanoparticles manufactured from eggshells at 900oC. XRD, FT-IR, SEM, BET, and TEM analyses were used to characterize the produced nanocomposites. The synthesized nanocomposite photocatalytic activity was evaluated by degrading MB dyes, its model of water pollution. The results showed that the nanocomposite CaO/AC/ZnO has a mesoporous structure with great sorption capability. Also, the photodegradation efficiency of MB using AC, CaO, AC/ZnO, and CaO/AC/ZnO nanocomposite was 33.23, 37.58, 54.61, and 88.92%, respectively, after100 min of sunlight irradiation indicating that photodegradation efficiency increases by improving the surface properties of AC. The CaO/AC/ZnO nanocomposite exhibited a 96.7% removal efficiency of MB following 120 min of visible light radiation exposure. Therefore, the CaO/AC/ZnO nanocomposite has a promising opportunity to function as a versatile and effective photocatalyst for photodegradation of organic dyes in wastewater.

Does the rate of metal salt precursor addition during ZIF-8 nanoparticles preparation affect their morphology?: Application in dye adsorption

Zeolitic imidazolate framework (ZIF)-8 nanoparticles demonstrate excellent physicochemical properties, which make them suitable for a variety of applications. However, their scale-up manufacturing requires insight into the rate of addition of precursors. This study investigates the impact of Zn salt precursor rate of addition to an organic linker solution on the morphology and size of ZIF-8 nanoparticles, and their potential for the adsorptive removal of dyes (cationic and anionic). ZIF-8 nanoparticles were produced with a molar ratio of Zn/2-methyl imidazole (Hmim)/H2O at 1/36/2206 by varying the flow rate of Zn precursor at 5, 10, 15, 20, and 25 mL/min into the Hmim solution. The physicochemical properties of the synthesized ZIF-8 nanoparticles were assessed using microscopy, analytical, and spectroscopy techniques. Owing to different flow rates of the precursor, variations in the ZIF-8 particles’ size and morphology were observed. It was found that the optimum flow rate was 15 mL/min (named Z-15), resulting in particle size of 261 nm, with a high specific surface area, thermal stability, and a substantially high yield of ∼89%. Furthermore, the dye adsorption studies, performed using Z-15 NPs, resulted in high methylene blue (∼82%) and methyl orange (∼76%) removal efficiency. The adsorption performance was maintained with dye-spiked simulated wastewater. The superior dye adsorption capacity of the ZIF-8 nanoparticles could be attributed to their microporous characteristics. Thus, this study demonstrates that the rate of addition of Zn precursor in the synthesis of ZIF-8, indeed, affects both their morphology and size, and the resulting nanoparticles exhibit promising adsorption performance toward dyes.

Removal of methylene blue using magnetic Na-bentonite composite in aqueous Solutions

The present work focuses on the development of a new magnetic composite material that would be practical and effective for the removal of methylene blue (MB) dye from water. This composite material was chemically prepared from bentonite and iron salts. It was characterized by ATR-FTIR, DRX, SEM and EDS. The adsorption study showed a relatively high adsorption capacity of MB on the composite (86.2mgg-1) and an MB removal efficiency of 100%. In a study of the influence of certain operating parameters, the effect of pH and temperature on MB removal efficiency was found to be negligible. However, the results of the kinetic and thermodynamic study showed that MB adsorption follows the pseudo-second- order and Langmuir model. Of the eluents tested, acetic acid proved to be the most efficient, with an MB desorption efficiency of 90%. The results obtained show that magnetic bentonite is an interesting solution for the removal of dyes in water by adsorption.

Novel mint-stalks derived biochar for the adsorption of methylene blue dye: Effect of operating parameters, adsorption mechanism, kinetics, isotherms, and thermodynamics

The pyrolysis of mint stalks and lemon peels was performed to synthesize mint-stalks (MBC) and lemon-peels (LBC) derived biochars for adsorbing methylene blue (MB). The preparation, characterization, and application of MBC in adsorption have not been reported in the literature. MBC showed higher surface area and carbon content than that of LBC. The removal ratios of MB were 87.5% and 60% within 90 min for MBC and LBC, respectively at pH 7, temperature of 30oC, adsorbent dose of 0.5 g/L, and MB concentration of 5 mg/L. The optimal MBC dose was 1 g/L achieving a removal efficiency of 93.6% at pH 7, temperature of 30oC, contact time of 90 min, and initial dye concentration of 5.0 mg/L. The adsorption efficiency decreased from 98.6% to 31.33% by raising the dye concentration from 3.0 mg/L to 30 mg/L. Further, the increase of adsorbent dose to 10 g/L could achieve 94.2%, 90.3%, 87.6%, and 84.1% removal efficiencies of MB in the case of initial concentrations of 200 mg/L, 300 mg/L, 400 mg/L, and 500 mg/L, respectively. MBC showed high stability in adsorbing MB under five cycles, and the performed analyses after adsorption reaffirmed the stability of MBC. The adsorption mechanism indicated that the adsorption of MB molecules on the biochar's surface was mainly because of the electrostatic interaction, hydrogen bonding, and π-π stacking. Pseudo-second-order and Langmuir models could efficiently describe the adsorption of MB on the prepared biochar. The adsorption process is endothermic and spontaneous based on the adsorption thermodynamics. The proposed adsorption system is promising and can be implemented on a bigger scale. Moreover, the prepared biochar can be implemented in other applications such as photocatalysis, periodate, and persulfate activation-based advanced oxidation processes.

Novel cow dung-doped sludge biochar as an efficient ozone catalyst: Synergy between graphitic structure and defects induces free radical pathways

A composite material, cow dung-doped sludge biochar (Zn@SBC-CD), was synthesized by one-step pyrolysis using ZnCl2 as an activating agent and applied to a catalytic ozonation process (COP) for methylene blue (MB) removal. SEM, XRD, FTIR, XPS and BET analyses were performed to characterize the biochar (BC) catalysts. Zn@SBC-CD had high graphitization degree, abundant active sites and uniform distribution of Zn on its surface. Complete removal of MB was achieved within 10 min, with a removal rate much higher than that of ozone alone (32.4%), implying the excellent ozone activation performance of Zn@SBC-CD. The influence of experimental parameters on MB removal efficiency was examined. Under the optimum conditions in terms of ozone dose 0.04 mg/mL, catalyst dose 400 mg/L and pH 6.0, COD was completely removed after 20 min. Electron paramagnetic resonance (EPR) analysis revealed radical and non-radical pathways were involved in MB degradation. The Zn@SBC-CD/O3 system generated superoxide anion radicals (•O2−), which were the main active species for MB removal, through adsorption, transformation, and transfer, Furthermore, Zn@SBC-CD exhibited good reusability and stability in cycling experiments. This study provides a novel approach for the utilization of cow dung and sludge in synthesis of functional biocatalysts and application in organic wastewater treatment.

Multiwalled carbon nanotubes@pectin/κ‐carrageenan‐based nanocomposite biohydrogel prepared by gamma irradiation for efficient methylene blue dye sequestration

AbstractThis study addresses the critical issue of removing toxic dyes from industrial wastewater to protect the environment and human health. To address this challenge, a bio‐based composite hydrogel was synthesized using gamma irradiation, 20 kGy, incorporating multiwalled carbon nanotubes@pectin/κ‐carrageenan/polyacrylic acid (MWCNTs PC/KC/PAAc) for removing methylene blue (MB) dye from aqueous solutions. The prepared composites underwent characterization through Fourier‐transform infrared spectroscopy, x‐ray diffraction, and thermogravimetric analyses. Brunauer–Emmett–Teller analysis demonstrated a significant increase in surface area upon the addition of MWCNTs. Specifically, the surface area increased from 342.5 m2 g−1 for PC/KC/PAAc to 689.5 m2 g−1 when 0.175 wt% of MWCNTs were added. Also, scanning electron microscopy and atomic force microscopy were utilized to examine the surface topography of PC/KC/PAAc and MWCNTs@PC/KC/PAAc. The results reveal that at 0.175 wt% of MWCNTs, there was a more uniform surface topography with well‐distributed MWCNTs within the matrix. In the adsorption study of MB dye, it was found that the highest MB removal efficiency was achieved at pH 11, with values of 68.21% and 96% for PC/KC/PAAc and MWCNTs@PC/KC/PAAc, respectively. Furthermore, upon studying the effect of MWCNTs (%), the results showed that the removal (%) of PC/KC/PAAc was 68.21 ± 1.02%, and this percentage increased rapidly with the addition of MWCNTs, reaching a maximum of 96 ± 0.85% when 0.175 (wt%) of MWCNTs was added. Isotherm and kinetic modeling demonstrated that MB adsorption follows the Freundlich isotherm for PC/KC/PAAc and the Redlich–Peterson isotherm for MWCNTs@PC/KC/PAAc, both following a pseudo‐second‐order kinetics model. In addition, from AFM data, after MB removal, the height increased significantly from 322 nm for PC/KC/PAAc to 810 nm for MWCNTs@PC/KC/PAAc (0.175 wt%), indicating a substantially higher adsorption of MB by MWCNTs@PC/KC/PAAc.

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%.

Microstructures, Optical, magnetic Properties, and photocatalytic activity of magnetically separable and reusable ZnO-Doped Fe3O4/rGO nanocomposite synthesized via green route

We report magnetically-separable, reusable, green-synthesized Fe3O4/rGO/ZnO, as heterogeneous catalyst for photo-Fenton degradation of organic pollutants in aqueous solution under certain treatments. Fe3O4 nanoparticles was green-synthesized using Moringa oleifera leaf extract, while rGO was synthesized utilizing Amaranthus viridis leaf extract. Fe3O4/rGO was composited under sonication treatment. Afterwards, Fe3O4/rGO was doped with ZnO with various concentration of ZnO. X-ray diffraction and selected area electron diffraction showed that Fe3O4 and ZnO had spinel cubic and hexagonal structure, respectively; another phase appeared as Fe2O3 spinel cubic structure. Crystallite size was decreased as the ZnO concentration increased. Morphology image showed almost spherical, non-uniform, and slightly dispersed particle under agglomerated condition, attaching to rGO sheets. The particle size of Fe3O4, Fe3O4/rGO, and Fe3O4/rGO/ZnO is 14.3; 14.1; and 10.4 nm, respectively. Fourier-transform infrared spectra showed metallic functional groups, such as Fe-O and Zn–O at 562–589 and 462–478 cm−1 also suggests nanocomposite formation. However, blue-shift absorption and band gap widening were observed with ZnO addition. Raman spectroscopy revealed the formation as-synthesized GO and rGO. Vibrating sample magnetometer showed that green-synthesized Fe3O4/rGO/ZnO exhibited superparamagnetic properties. Removal efficiency of photodegradation methylene blue was optimal for green-synthesized Fe3O4/rGO/ZnO under sonication treatment, reached 100 % degradation within 180 min for uptake every 30 min. Photodegradation was also analyzed using Langmuir-Hinshelwood kinetic model, resulting rate constant of 24.7 × 10−3 min−1 and half-life time of 28.1 min at optimum treatment. Reusability of photocatalytic activity after 3 cycles showed only a tiny drop in catalytic efficiency. Meanwhile, it possesses high stability in catalytic activity and structure. The green-synthesized Fe3O4/rGO/ZnO potential as an environmentally friendly reusable photocatalyst for wastewater degradation.

Development of a novel Z-scheme CoxNi1−xTiO3/CdS (x = 0.5) photocatalyst for the efficient degradation of organic pollutants via a visible-light-driven photocatalytic process

Herein, for the first time, we reported the synthesis of a novel Z-scheme CoxNi1−xTiO3/CdS (x = 0.5) heterojunction photocatalyst and the investigation of its visible-light-driven photocatalytic performance toward degradation of methylene blue (MB). The developed photocatalyst was structurally characterized by applying X-Ray diffraction analysis (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), differential reflectance spectroscopy (DRS), and photoluminescence (PL) techniques. The results indicated the formation of a highly porous structure with improved visible light adsorption capacity, favorable for the catalytic activity. At an optimum condition of 10 mg/L of MB and 300 mg/L of catalyst, the ternary photocatalyst demonstrated a MB removal efficiency of 99 % after 75 min of the treatment process. The radical trapping experiments unveiled that hydroxyl and superoxide radicals were two main reactive species formed under visible light, while the valance holes possessed an insignificant role. The synergetic impact of the CoxNi1−xTiO3 (x = 0.5) and CdS on the photodegradation of MB over the as-prepared CoxNi1−xTiO3/CdS (x = 0.5) photocatalyst through Z-scheme photocatalysis was indicated by the results of the mechanism studies. The percentage impact of the treatment time, MB concentration, the ratio of CoxNi1−xTiO3/CdS (x = 0.5), and the dosage of catalyst using analysis of the CCD modeling was obtained as 47.04, 16.67, 7.22 and 0.87 %, respectively. Furthermore, the as-synthesized photocatalyst possessed high recyclability and photostability with only a 3 % decline in activity after four repetitive cycles.

The Effect of Silica Concentration on The Absorption Properties of Silica-Based Ceramic Membrane

Water pollution is currently an increasingly widespread environmental problem. Methylene blue is a synthetic dye used in the textile industry which pollutes the aquatic environment. The absorption of Methylene Blue textile dye which pollutes the environment uses silica precipitate as a filler in ceramic membranes with a clay matrix. Silica precipitate added to the ceramic membrane varies with a concentration of 0.3 %, 1.01 %, 1.68 %, 2.34 % and 2.99 %. The membrane will be characterized using Fourier Transform Infrared (FTIR) testing to determine the functional groups of the components it contains. Testing the absorption of methylene blue contaminant content from artificial wastewater using the UV-Vis Spectrophotometry test. The FTIR test carried out compared the functional groups of membrane samples before and after sintering. The results obtained from the FTIR test were that the membrane after sintering contained silica and some PEG, while the membrane before sintering contained other components such as PVA, PEG, water molecules and silica. The UV-Vis test carried out on the membrane gave results that the membrane was 0.3 %, 1.01 %, 1.68 %, 2.34 % and 2.99 % respectively has a removal efficiency of 58.0 %, 54.0 %, 59.3 %, 64.0 % and 66.4 %, where the best removal efficiency of methylene blue was on a membrane filled with 2.99 % of silica. Tests on the membrane showed that an increase in silica concentration was in line with an increase in the quality of the membrane’s performance in rejecting methylene blue contaminants.

Recycling alkali lignin-derived biochar with adsorbed cadmium into cost-effective CdS/C photocatalyst for methylene blue removal.

Cadmium (Cd)-enriched adsorbents wastes possess great environmental risk due to their large-scale accumulation and toxicity in the natural environment. Recycling spent Cd-enriched adsorbents into efficient catalysts for advanced applications could address the environmental issues and attain the carbon neutral goal. Herein, a facile strategy is developed for the first time to reutilize the alkali lignin (AL)-derived biochar (ALB) absorbed with Cd into cadmium sulphide (CdS)/C composite for the efficient methylene blue (MB) removal. The ALB is initially treated with Cd-containing solution, then the recycling ALB samples with adsorbed Cd are converted to the final CdS/C composite using NaS2 as the sulphurizing reagent for vulcanization reaction. The optimal ALB400 demonstrates a high adsorption capacity of 576.0 mg g-1 for Cd removal. Then the converted CdS/C composite shows an efficient MB removal efficiency of 94%. The photodegradation mechanism is mainly attributed to carbon components in the CdS/C composite as electron acceptor promoting the separation of photoelectrons/holes and slowing down the abrasion of CdS particles. The enhanced charge transfer and contact between the carrier and the active site thus improves the removal performance and reusability. This work not only develops a method for removing Cd from wastewater effectively and achieving the waste resource utilization but also further offers a significant guidance to use other kinds of spent heavy metal removal adsorbents for the construction of low-cost and high value-added functional materials.

MnOx-Coffea arabica Husk and Catha edulis Leftover Biochar Nanocomposites for Removal of Methylene Blue from Wastewater.

In this study, we investigated the use of manganese oxide-biochar nanocomposites (MnOx-BNC), synthesized from coffee husk (CH) and khat leftover (KL) for the removal of methylene blue (MB) from wastewater. Pristine biochars of each biomass (CH and KL) as well as their corresponding biochar-based nanocomposites were synthesized by pyrolyzing at 300°C for 1 h. The biochar-based nanocomposites were synthesized by pretreating 25 g of each biomass with 12.5 mmol of KMnO4. To assess the MB removal efficiency, we conducted preliminary tests using 0.2 g of each adsorbent, 20 mL of 20 mg·L-1 MB, pH 7.5, and shaking the mixture at 200 rpm and for 2 h at 25°C. The results showed that the pristine biochar of CH and KL removed 39.08% and 75.26% of MB from aqueous solutions, respectively. However, the MnOx-BNCs removed 99.27% with manganese oxide-coffee husk biochar nanocomposite (MnOx-CHBNC) and 98.20% with manganese oxide-khat leftover biochar nanocomposite (MnOx-KLBNC) of the MB, which are significantly higher than their corresponding pristine biochars. The adsorption process followed the Langmuir isotherm and a pseudo-second-order model, indicating favorable monolayer adsorption. The MnOx-CHBNC and MnOx-KLBNC demonstrated satisfactory removal efficiencies even after three and six cycles of reuse, respectively, indicating their potential effectiveness for alternative use in removing MB from wastewater.