Search Results (1,539)

MgCr2O4 nanospinel samples were synthesized using a modified Pechini method, followed by controlled calcination. The resulting materials were evaluated in terms of crystal structure, particle morphology, and optical and electronic properties. Their oxidative activity towards the degradation of organic dyes was investigated via photocatalysis, Fenton-like, and photon-Fenton-like processes. Various analytical techniques were employed to characterize the samples, including X-ray diffraction (XRD) with Rietveld refinements, infrared (IR) spectroscopy, UV–Vis spectroscopy, colorimetry, and transmission and high-resolution transmission electron microscopy (TEM/HRTEM). Structural characterization revealed that MgCr2O4 crystallized after calcination at 600 ${}^{\circ }$C, and Rietveld refinements confirmed cubic Fd-3m symmetry. IR spectra confirmed the short-range order through the presence of vibrational modes assigned to CrO6^2- octahedra. UV–Vis spectroscopy indicated mixed Cr valences (Cr³+/Cr⁶+) for samples calcined at temperatures below 900 ${}^{\circ }$C, with Cr⁶+ eliminated at higher temperatures, confirmed by electron paramagnetic resonance (EPR) spectroscopy. This suggests that an oxidation reaction occurred due to oxygen vacancies in the lattice. Optical bandgap (Eg) increased with temperature. Samples calcined at low temperatures were dark green and became more saturated at temperatures above 900 ${}^{\circ }$C, suggesting photoresponse to visible light, as indicated by the Eg values. The oxidative activity of the nanospinels in degrading the dyes methylene blue (MB) and rhodamine B (RhB) under visible light depended on the nature of the dye, the catalyst concentration, and the use of H2O2 in the process to improve the formation of hydroxyl radicals (•OH), as confirmed by photohydroxylation of terephthalic acid (TA). The highest degradation rate was observed in the photo-Fenton-like process, with 96% and 97% degradation of RhB and MB dyes in 60 min, reaching a kinetic rate constant (${\mathit{K}}_{app}$) of 0.055 min${}^{-1}$ and 0.051 min${}^{-1}$, respectively. This study highlights the importance of controlling various parameters to promote the formation of reactive oxygen species (ROS) required for oxidative degradation by nanospinels. Full article

This study investigates the potential of several sustainable agricultural by-products—including olive stones, cork, and almond shells, which are locally available in Alentejo, Portugal—as low-cost adsorbents for the removal of methylene blue (MB) from synthetic wastewater. The biomass residues were evaluated both in their raw form and after conversion into activated carbons (ACs) through chemical activation with KOH at 973 K. The produced ACs exhibited well-developed surface areas (760–1103.5 m² g⁻¹) and porous structures (0.31–0.51 cm³ g⁻¹). The adsorbents were characterised in terms of their chemical and textural properties. Raw biomass materials presented acidic surface groups, whereas the ACs presented neutral or basic groups. Batch adsorption experiments were conducted to assess the effects of adsorbent particle size, solution pH, initial MB concentration, stirring speed, contact time, and temperature on dye removal efficiency. Among all tested materials, the ACs achieved superior MB adsorption capacities, ranging from 244.2 to 317.6 mg g⁻¹, compared to the untreated biomass adsorbents, which showed capacities between 34.1 and 46.4 mg g⁻¹. The adsorption data were best described by the Langmuir isotherm model, while the kinetic data closely followed the pseudo-second-order (PSO) model. Thermodynamic analysis revealed that MB adsorption was spontaneous and endothermic; however, the relatively low enthalpy values indicated that physical interactions contributed significantly, particularly in the case of the raw biomass adsorbents. This suggests that the PSO model may also be applicable when physical adsorption is the dominant mechanism. This work demonstrates the novel use of cork, olive stone, and almond shell biomasses and their derived ACs as sustainable adsorbents, highlighting an integrated approach that simultaneously promotes efficient wastewater treatment, waste valorisation, and circular economy-driven socio-economic development. Full article

In this work, ZnO nanoparticles were synthesized via a plant-mediated green route using Prosopis tamaulipana extract as a reducing and stabilizing agent and subsequently modified with silver to obtain Ag-modified ZnO powders. Structural and morphological characterization techniques confirmed the formation of nanocrystalline ZnO with a hexagonal wurtzite structure, submicrometric agglomerates composed of nanosized primary particles and a high degree of phase purity, indicating the effectiveness of the synthesis approach. The photocatalytic performance of the Ag-modified ZnO materials was evaluated under natural solar irradiation using methylene blue as a model organic contaminant in aqueous solution. Visual observations, together with absorbance, temperature and electrical conductivity measurements, demonstrated an effective and progressive degradation of the dye over a 5 h irradiation period. The observed increase in electrical conductivity under illumination was associated with enhanced charge carrier generation and improved separation efficiency, as well as the formation of reactive oxygen species, promoted by the presence of Ag as an electron sink. These results confirm that green-synthesized Ag-modified ZnO nanoparticles exhibit enhanced photocatalytic activity and are promising multifunctional materials for sustainable water sanitation applications. Full article

In this work, monodisperse carbon microspheres with an average diameter of approximately 900 nm were successfully synthesized via a hydrothermal method. To further tailor their surface properties, the layer-by-layer (LbL) self-assembly technique was employed, where the cationic polyelectrolyte poly(diallyldimethylammonium chloride) (PDDA) and the anionic polyelectrolyte poly(styrene sulfonate) (PSS) were alternately deposited on the microsphere surface, forming two and four bilayer assemblies, respectively. The resulting composite microspheres exhibited remarkable adsorption performance toward representative dyes in water solution, such as rhodamine B (RhB) and methylene blue (MB). Experimental results demonstrated that the incorporation of a single bilayer significantly reduced the specific surface area but introduced additional active adsorption sites, thereby enhancing dye removal efficiency. However, when the number of bilayers was further increased to two, partial pore coverage and blockage occurred, leading to a reduced surface area and consequently diminished adsorption capacity. These findings highlight that in LbL surface modification, more layers do not necessarily yield better performance, but rather an optimal assembly thickness exists. This insight provides valuable guidance for the rational design of advanced adsorbent materials for wastewater treatment. Full article

Geopolymers, alkali-activated aluminosilicate materials, have gained increasing attention as sustainable adsorbents for wastewater treatment due to their low-temperature synthesis, cost-effectiveness, and ease of shaping into mechanically robust structures. Their intrinsic negatively charged framework promotes the adsorption of cationic species; however, pristine geopolymers typically exhibit moderate performance, with adsorption capacities generally below ~70 mg g⁻¹ for dyes such as methylene blue (MB) and in the range of 20–100 mg g⁻¹ for divalent metal ions. To overcome these limitations, different strategies have been developed to tailor their pore structure and surface chemistry. In particular, foaming approaches enable the production of highly porous materials with tunable pore architecture, improving mass transfer and accessibility of active sites. Moreover, functionalization with carbon-based materials (e.g., activated carbon, graphene derivatives, biochar) or zeolitic phases significantly enhances adsorption performance, with reported capacities exceeding 500 mg g⁻¹ for Pb²⁺ and up to 450 mg g⁻¹ for organic dyes in optimized systems. This review provides a comprehensive overview of recent advances in geopolymer synthesis, pore engineering, and functionalization strategies, highlighting the relationships between composition, structure, and adsorption performance. Particular attention is devoted to the comparison between carbon-based and zeolitic modifications, as well as to the role of material shaping in enabling practical applications. Overall, the combination of tunable porosity, chemical versatility, and structural integrity positions functionalized geopolymers as promising candidates for the development of scalable and multifunctional adsorbents for wastewater remediation. Full article

Semiconductor photocatalysis technology is a simple, efficient, and low-cost method for environmental pollution remediation. As a promising photocatalyst for oxidative degradation, titanium dioxide (TiO₂) demonstrates the capability to address energy shortages and environmental pollution issues. In this study, orange peel was used as the raw material to synthesize a (TiO₂-CdS-C₃N₄-CDs) TCCC composite photocatalyst containing natural green carbon dots via a one-pot hydrothermal method for the first time. This catalyst was applied to the catalytic degradation of multiple dye molecules (Rhodamine B, Methylene Green, Reactive Brilliant Blue KN-R) and quinolone antibiotic (Ciprofloxacin, CIP) as well as tetracycline antibiotic (Tetracycline, THC). Meanwhile, it provides more adsorption sites for target pollutants and loads electron reservoirs (CDs) on the TCC surface, promoting the separation of photogenerated carriers in pure TiO₂, thereby enhancing the visible light utilization and photocatalytic activity of the material. This work expands the application scope of semiconductor photocatalysis technology and TiO₂-based photocatalytic active substrates. Full article

Background: Lateral epicondylopathy is commonly approached as a tendinopathic disorder of the common extensor origin; however, persistent lateral elbow pain may also involve a superficial sensory nerve component related to the posterior antebrachial cutaneous nerve (PABCN). This proof-of-concept cadaveric anatomical feasibility study evaluated whether a single-window, humerus-parallel ultrasound-guided injectate pathway could simultaneously reach the superficial PABCN-related fascial plane and the common extensor origin. Methods: One fresh-frozen male cadaveric donor was used, and both elbows were injected under real-time ultrasound guidance. With the elbow flexed and the forearm pronated, the transducer was aligned parallel to the long axis of the humerus over the lateral epicondylar region. A 23-gauge, 6 cm needle was advanced in plane from distal to proximal over the common extensor aponeurosis, and 10 mL of 1% methylene blue was injected into each elbow. Layer-by-layer anatomical dissection was then performed by an anatomist who was not involved in the injection procedure. Gross linear dye spread was measured directly during dissection using the distal needle entry point as the reference point, and ruler-containing photographs were additionally reviewed using ImageJ software for supportive image-assisted assessment. Results: In both elbows, methylene blue stained the superficial PABCN-related fascial plane, including the anterior and posterior branches of the PABCN, and concomitantly covered the common extensor aponeurosis and lateral epicondylar enthesis. Dye spread measured approximately 10 cm proximally, 5 cm distally, and 4 cm anteriorly. No gross intra-articular dye deposition or focal intramuscular pooling was observed. Conclusions: This proof-of-concept cadaveric study demonstrates the anatomical plausibility of a single-window, enthesis-centered ultrasound-guided injectate pathway that includes both the superficial PABCN-related plane and the common extensor origin. These findings should be interpreted as descriptive anatomical feasibility observations and do not establish reproducibility across anatomical variants, clinical efficacy, safety, or procedural superiority. Full article

This work reports the synthesis, characterization, and photocatalytic performance of multifunctional spheres based on AgNP-doped TiO₂-Fe₃O₄ embedded in an alginate–chitosan biopolymeric matrix for the removal of organic contaminants from water. The composite powders exhibited a nanocrystalline structure composed of anatase TiO₂ (~20 nm) and magnetite (~25 nm), with homogeneously dispersed Ag nanoparticles, as observed by SEM. The spheres presented a mainly submicrometric particle size distribution (0.55–0.92 µm), favoring high surface area and colloidal stability. Under simulated solar irradiation, the material achieved efficient photocatalytic degradation of methylene blue, with a pseudo-first-order rate constant of 0.112 h⁻¹ and ~46% decolorization after 5 h. UV-Vis spectra showed progressive attenuation of the dye absorption band without accumulation of intermediates. Magnetic recovery tests confirmed rapid separation and reuse without performance loss. The enhanced activity is attributed to the synergistic interaction among plasmonic Ag, photocatalytic TiO₂, redox-active Fe₃O₄, and the adsorptive carbon–biopolymer matrix. The material exhibited strong antibacterial activity, achieving over 90% removal of fecal coliforms after 5 h of irradiation. Therefore, the developed AgNP-doped TiO₂-Fe₃O₄ spheres represent a sustainable, reusable, and efficient material for solar-assisted water sanitation. Full article

Increasing volumes of dye-containing wastewater generated by the textile industry have become a serious environmental issue, particularly in Indonesia, where textile production contributes substantially to industrial activity. Among synthetic dyes, methylene blue (MB) is widely used because of its low cost and high solubility in water; however, its persistence, toxicity, and potential carcinogenicity make its removal from wastewater highly important. Conventional treatment methods are often limited by incomplete degradation and secondary waste generation. In this study, iron oxide nanoparticles (IONPs) were synthesized through a green route using Psidium guajava leaf extract as both a reducing and stabilizing agent. Characterization by PSA, UV-Vis, SEM-EDX, and XRD confirmed the formation of magnetite-like iron oxide particles with sizes ranging from 209.2 to 291.4 nm. Photocatalytic experiments showed high MB degradation efficiency (94.7–99.0%) under UV irradiation, highlighting the potential of guava leaf-mediated IONPs as low-cost, sustainable photocatalysts for wastewater treatment. Full article

The development of high-performance adsorbents for treating dye-laden wastewater necessitates a deep understanding of structure–property relationships. This study presents a systematic investigation into the role of carbon material dimensionality (0D biochar, BC; 1D carbon nanotubes, CNT; 2D graphene oxide, GO) in modulating the properties of a dual physically crosslinked sodium alginate/polyacrylamide (SA/PAM) hydrogel for methylene blue (MB) adsorption. A series of composite hydrogels was fabricated via a sequential physical crosslinking strategy. Comprehensive characterization confirmed the successful incorporation and dispersion of carbon materials within the dual network. The three hydrogels showed good mechanical properties. Under the conditions of 25 °C, an initial MB concentration of 100 mg/L, and pH 10–11, the incorporation of carbon materials enhanced the adsorption capacity, with maximum adsorption capacities of 411.5, 410.6, and 422.8 mg/g for BC-H, GO-H, and CNT-H, respectively. Coexisting constituents in real water samples reduce adsorption capacity via competitive adsorption and interfacial interference. After five consecutive adsorption–desorption cycles, the adsorption capacities of BC-H, GO-H, and CNT-H decreased to 57.7%, 67.2%, and 61.7% of their initial values, respectively. Adsorption isotherm and kinetic studies revealed that the process followed the Langmuir model and pseudo-second-order kinetics, indicative of monolayer chemisorption. Mechanistic analysis identified synergistic contributions from electrostatic attraction, π-π stacking, and physical entrapment. Physical structural changes and chemical site occupation are the main reasons for the decrease in the adsorption performance of hydrogels during cyclic use. This work provides a rational design strategy for advanced adsorbents and a theoretical foundation for efficient dye wastewater remediation. Full article

In this study, manganese ferrite was grown on the surface of a low-cost powder substrate of a guava leaf using the co-precipitation method. The resulting material was characterized using various spectroscopic and microscopic techniques. The composite was formed through the electrostatic and non-electrostatic interactions between the manganese ferrite nanoparticles, and the functional groups present on the guava leaf substrate; consequently, a high content of functional groups was observed in the synthesized composite through the Fourier transform infrared spectroscopy. The average size of the nanoparticles grown on the guava leaf substrate was determined to be between 3 and 5 nanometers. The synthesized composite material was utilized for adsorption applications, employing Methylene blue dye as a model adsorbate. Methylene blue was removed from the aqueous solutions under various conditions—including variations in the pH, contact time, temperature, and concentration. Under optimal conditions, it was observed that an adsorbent dosage of 2 g L⁻¹ was capable of removing approximately 99% of the dye from a 10 mg L⁻¹ dye solution at pH 7. The dye removal efficiency (%) decreased with the increasing temperature, indicating an exothermic process; this was further confirmed by the thermodynamic parameter analysis (specifically, the change in enthalpy, or ΔH), which yielded a negative value. Gibbs Free Energy (ΔG) also yielded a negative value, signifying the feasibility and spontaneity of the adsorption process. In this study, the adsorption process followed the Freundlich isotherm model, with the value of ‘n’ falling between 1 and 10, which is indicative of heterogeneous adsorption. The adsorption kinetics were determined to follow a pseudo-second-order model, and the overall rate-limiting step of the process was identified as intraparticle diffusion. To assess the sustainability and stability of the adsorbent, regeneration and reusability experiments were conducted. The results revealed that the modified guava leaf performed effectively for up to five cycles, achieving an adsorption efficiency of approximately 24% after the final cycle. Thus, the developed adsorbent proved to be an effective material for the removal of Methylene blue dye. Full article

The massive discharge of methylene blue causes severe water pollution, and the development of efficient and stable heterogeneous Fenton catalysts is crucial for wastewater treatment. To address the shortcomings of traditional iron-based amorphous catalysts, such as low activity and poor stability, this study employed Fe₈₀Si₆B₁₀Cu₁Nb₃ five-component amorphous alloy as the catalyst to investigate its catalytic degradation performance, cyclic stability, and catalytic mechanism for MB. Batch experiments, SEM, XRD characterization, and kinetic fitting were combined to carry out the research. The results showed that under the optimal conditions (25 °C, pH = 3, H₂O₂ concentration of 5 mM, catalyst dosage of 0.5 g/L), the catalyst could completely degrade methylene blue within 9 min with a reaction rate constant k_obs of 0.44 min⁻¹, and the degradation efficiency showed no obvious attenuation after 20 consecutive cyclic degradation runs. After degradation, slight selective corrosion occurred on the catalyst surface, while the amorphous structure of the matrix remained stable. This study confirms that the Cu/Nb dual synergy improves the catalytic performance and stability, clarifies the relevant catalytic mechanism, and provides theoretical and technical support for the design of high-performance iron-based amorphous catalysts and the treatment of dye-containing wastewater. Full article

This study presents the synthesis and use of a novel bamboo-derived magnetic activated carbon (BMAC) for the effective removal of cationic and anionic dyes, specifically methylene blue (MB), methyl orange (MO), and sunset yellow (SY), from aqueous solutions. The adsorbent was synthesized using thermal carbonization and subsequent inclusion of magnetic oxide, yielding a porous structure with improved adsorption and magnetic separation properties. Thorough characterization utilizing SEM, EDX, BET, FTIR, XRD, and TGA/DTA validated the creation of a highly porous material including uniformly dispersed magnetic particles and several surface functional groups. Batch adsorption tests were performed to examine the influences of contact time, adsorbent dosage, initial dye concentration, pH, and temperature. The findings indicated rapid adsorption kinetics, with equilibrium reached in around 60–70 min, and adsorption capacity ranked as MB > MO > SY. Augmenting adsorbent dosage enhanced removal efficiency but diminished adsorption capacity per unit mass due to site unsaturation. The maximum adsorption capacities (q_m) of BMAC were 58.9, 56.3, and 32.7 mg/g for MB, MO, and SY, respectively, as determined from the Langmuir isotherm model, indicating superior performance compared with other reported magnetic activated carbon. The adsorption process was determined to be exothermic and spontaneous, as evidenced by thermodynamic characteristics. The equilibrium data were optimally characterized by the Langmuir isotherm model, indicating monolayer adsorption, whereas the kinetic studies conformed to the pseudo-second-order model, signifying that chemisorption is predominant. The adsorption mechanism encompasses electrostatic interactions, π–π stacking, hydrogen bonding, van der Waals forces, pore filling, and surface complexation with magnetic oxides. The findings indicate that BMAC is an efficient, sustainable, and magnetically recoverable adsorbent for the elimination of both cationic and anionic dyes from wastewater. Full article

The development of adsorbents with high adsorption capacity, easy separation, and good reusability is critical for the treatment of dye-contaminated wastewater. Herein, a novel magnetic composite hydrogel, P(AA-AM)/SA-BC-Fe₃O₄, was synthesized via free radical polymerization, integrating acrylic acid (AA), acrylamide (AM), sodium alginate (SA), biochar (BC), and magnetic Fe₃O₄ nanoparticles. The material was systematically characterized by FTIR, XRD, SEM, BET, and VSM, which confirmed the successful formation of a three-dimensional porous network with well-dispersed Fe₃O₄ nanoparticles and BC, endowing the hydrogel with superparamagnetic properties. The adsorption performance of the hydrogel towards methylene blue (MB) was evaluated under various conditions. The results demonstrated that the adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm, indicating that chemisorption is an important mechanism in the monolayer adsorption process. The hydrogel exhibited excellent swelling properties and remarkable pH-dependent adsorption behavior, with optimal performance in weakly alkaline environments. Notably, the incorporation of BC enhanced the adsorption capacity, while Fe₃O₄ enabled rapid magnetic separation, with the adsorbent retaining approximately 77% of its initial capacity after five regeneration cycles. This work presents a promising strategy for constructing magnetic hydrogel adsorbents that synergistically combine high adsorption efficiency, facile separability, and good reusability for practical wastewater treatment applications. Full article

Hexagonal boron nitride (h-BN) is a chemically stable two-dimensional material whose wide band gap and low surface reactivity limit its performance in adsorption and photocatalysis, motivating strategies to tailor its structure. In this work, a mechanochemical approach combining high-energy ball milling with NaOH-assisted treatment was used to induce simultaneous exfoliation and hydroxylation of h-BN, promoting defect generation, reduced crystallinity, interlayer expansion, and incorporation of oxygen-containing groups (B-OH and B-O). These modifications led to band gap narrowing, increased surface polarity, and improved dispersion, enabling the formation of heterogeneous active sites. The hydroxylated material (BN-OH) exhibited high adsorption capacities of 248 mg/g for methylene blue (MB) and 215 mg/g for rhodamine 6G (R6G), following Freundlich behavior, indicative of heterogeneous adsorption governed by electrostatic interactions, π–π stacking, hydrogen bonding, and defect-mediated sites. Under solar irradiation, BN-OH achieved up to 99% degradation of both dyes, following predominantly pseudo-first-order kinetics and outperforming pristine BN; additionally, the kinetic behavior under solar conditions was successfully described using the Behnajady–Modirshahla–Ghanbary (BMG) model, which accurately predicts the two-stage degradation process. Scavenger experiments revealed that ⦁OH radicals dominate MB degradation, while ⦁OH, O₂⦁⁻, and h⁺ contribute to R6G removal. Overall, defect engineering and hydroxyl functionalization synergistically enhance photocatalytic performance, providing a scalable strategy for wastewater treatment. Full article