Search Results (1,744)

This study considered and compared silver, gold, and their combination of nanoparticles (AgNPs, AuNPs, and Au-AgNPs) with biocompatible material mesoporous silica SBA-15 as potential antibacterial agents. A facile, one-pot “green” methodology, utilizing L-histidine as a reducing agent and bridge between components, was employed to obtain Ag@SBA-15, Au@SBA-15, and Au-Ag@SBA-15 nanocomposites without the use of external additives. Various physicochemical tools (UV-Vis, TEM, SAED, FESEM, XPS, BET, XRD, and FTIR) presented SBA-15 as a good carrier for spherical AgNPs, AuNPs, and Au-AgNPs with average diameters of 8.5, 16, and 9 nm, respectively. Antibacterial evaluations of Escherichia coli and Staphylococcus aureus showed that only Ag@SBA-15, at a very low Ag concentration (1 ppm) during 2 h of contact, completely reduced the growth (99.99%) of both strains, while the Au@SBA-15 nanocomposite required higher concentrations (5 ppm) and time (4 h) to reduce 99.98% E. coli and 94.54% S. aureus. However, Au introduction in Ag@SBA-15 to form Au-Ag@SBA-15 negatively affected its antibacterial potential, lowering it due to the galvanic replacement reaction. Nevertheless, the rapid and effective combating of two bacteria at low NPs concentrations, through the synergistic effects of mesoporous silica and AgNPs or AuNPs, in Ag@SBA-15 and Au@SBA-15 nanocomposites, provides a potential substitute for existing bacterial disinfectants. Full article

The escalating issue of water pollution driven by rapid industrialization necessitates the development of advanced remediation technologies. In this study, a novel method for producing chromium (Cr(VI)) ion-imprinted biochar (Cr(VI)-IIP-PEI@NBC) from wheat residue was proposed. After acid-oxidative modifications, polyethyleneimine (PEI) and glutaraldehyde (GA) were employed as the functional monomer and crosslinker, respectively, to enhance the biochar’s selectivity and adsorption capacity. Under optimized conditions (pH 2.0, 55 °C), the adsorbent achieved a maximum Cr(VI) uptake of 212.63 mg/g, which was 2.3 times higher than that of the non-imprinted biochar. The material exhibited exceptional specificity (99.64%) for Cr(VI) and maintained >80% adsorption efficiency after five regeneration cycles, demonstrating excellent reusability. Comprehensive structural characterization via Fourier transform infrared spectroscopy (FT-IR), thermal gravimetric analysis (TGA), Brunner–Emmet–Teller measurements (BET), and Scanning Electron Microscopy (SEM) confirmed successful Cr(VI) imprinting in the biochar and its high thermal stability and mesoporous architecture, elucidating the mechanisms behind its superior performance. This study presents a sustainable and high-performance adsorbent for the efficient treatment of chromium-contaminated wastewater, with significant potential for industrial applications. Full article

TiO₂ is the most used material for the photocatalytic removal of organic pollutants in aqueous media. TiO₂, specifically its anatase phase, is well-known for its great performance under UV irradiation, high chemical stability, low cost and non-toxicity. Nevertheless, TiO₂ presents two main drawbacks: its limited absorption of the visible spectrum; and its relatively low specific surface area and pore volume. Regarding the latter, several works in the literature have addressed the issue by developing new synthesis approaches in which anatase is dispersed and supported on the surface of porous materials. In the present work, two series of materials have been prepared where anatase has been supported on mesoporous silica (MSTiR%) in situ through a hydrothermal synthesis approach, where, in addition to using tetraethoxysilane (TEOS) as a silicon precursor, three organotriethoxysilanes [RTEOS, where R = methyl (M), propyl (P) or phenyl (Ph)] were used at a RTEOS:TEOS molar percentage of 10 and 30%. The materials were thoroughly characterized by several techniques to determine their morphological, textural, chemical, and UV-vis light absorption properties and then the most promising materials were used as photocatalysts in the photodegradation of the emerging contaminant and antiepileptic carbamazepine (CBZ) under UV irradiation. The materials synthesized using 10% molar percentage of RTEOS (MSTiR10) were able to almost completely degrade (~95%), 1 mg L⁻¹ of CBZ after 1 h of irradiation using a 275 nm LED and 0.5 g L⁻¹ of catalyst dose. Therefore, this new synthesis approach has proven useful to develop photoactive TiO₂ composites with enhanced textural properties. Full article

To address the challenges of complex composition, high chemical oxygen demand (COD) content, and the difficulty of treating organic wastewater from brewery wastewater, as well as the limitations of traditional Fenton technology, including low catalytic activity and high material costs, this study proposes the use of biochemical sludge as a raw material. Coupled with iron salt activation and mechanical ball milling technology, a low-cost, high-performance iron-doped mesoporous nano-sludge biochar material is prepared. This material was employed as a particle electrode to construct a three-dimensional electro-Fenton system for the degradation of organic wastewater from sauce-flavor liquor brewing. The results demonstrate that the sludge-based biochar produced through this approach possesses a mesoporous structure, with an average particle size of 187 nm, a specific surface area of 386.28 m²/g, and an average pore size of 4.635 nm. Iron is present in the material as multivalent iron ions, which provide more electrochemical reaction sites. Utilizing response surface methodology, the optimized treatment process achieves a maximum COD degradation rate of 71.12%. Compared to the control sample, the average particle size decreases from 287 μm to 187 nm, the specific surface area increases from 44.89 m²/g to 386.28 m²/g, and the COD degradation rate improves by 61.1%. Preliminary investigations suggest that the iron valence cycle (Fe²⁺/Fe³⁺) and the mass transfer enhancement effect of the mesoporous nano-structure are keys to efficient degradation. The Fe-O-Si structure enhances material stability, with a degradation capacity retention rate of 88.74% after 30 cycles of use. When used as a particle electrode to construct a three-dimensional electro-Fenton system, this material demonstrates highly efficiency in organic matter degradation and shows promising potential for application in the treatment of organic wastewater from sauce-flavor liquor brewing. Full article

Mesoporous silica nanoparticles have been synthesized through sol–gel synthesis in basic conditions. Gemini surfactants having urea in the headgroups were used as pore-forming agents. The effect of the spacer length of the surfactant on the particle morphology was studied on the sub-micrometer and nanometer scales using nitrogen porosimetry, small-angle X-ray scattering (SAXS), ultra-small-angle neutron scattering, and scanning and transmission electron microscopy (SEM, TEM). Depending on the spacer, spherical and/or cylindrical nanoparticles formed in different proportions, as revealed by statistical analysis of SEM micrographs. All prepared materials showed the hexagonal pore structure characteristic of the MCM-41 molecular sieves, with the exception of the sample prepared using the gemini surfactant with the shortest spacer length. The influence of the spacer length on the lattice parameter of the pore network, as well as the average size of the ordered domains, has been assessed by SAXS and TEM. Detailed analysis of the TEM images revealed a spread of the lattice parameter in a range of 10–20%. The broadening of the diffraction peaks was shown to be due to the combination of the effects of the finite domain size and the variance of the lattice parameter across the crystalline domains. The structural differences between the silica gels synthesized with the different surfactants were related to the variation of the micelle morphologies, reported in previous light scattering and small-angle scattering experiments. No connection could be revealed between the micelle shape and size and the pore sizes, showing that surfactants with a broad range of spacer lengths can equally well be used for the preparation of MCM-41 materials. Full article

Dry reforming of methane and ethanol is a promising catalytic process for the conversion of carbon dioxide and hydrocarbon feedstocks into synthesis gas (H₂/CO), which serves as a key platform for the production of fuels and chemicals. Over the past decade, substantial progress has been achieved in the design of catalysts with enhanced activity and stability under the demanding conditions of these strongly endothermic reactions. This review summarizes the latest developments in catalyst systems for DRM and EDR, including Ni-based catalysts, perovskite-type oxides, MOF-derived materials, and high-entropy alloys. Particular attention is given to strategies for suppressing carbon deposition and preventing metal sintering, such as oxygen vacancy engineering in oxide supports, rare earth and transition metal doping, strong metal–support interactions, and morphological control via core–shell and mesoporous architectures. These approaches have been shown to improve coke resistance, maintain metal dispersion, and extend catalyst lifetimes. The review also highlights emerging concepts such as multifunctional hybrid systems and innovative synthesis methods. By consolidating recent findings, this work provides a comprehensive overview of current progress and future perspectives in catalyst development for DRM and EDR, offering valuable guidelines for the rational design of advanced catalytic materials. Full article

Nitrogen (N) and phosphorus (P) play vital roles in crop growth. However, conventional fertilizers exhibit low utilization efficiency, making them prone to causing resource wastage and water eutrophication. Although metal–organic frameworks (MOFs) have shown great potential for application in controlled-release fertilizers (CRFs), currently reported MOF-based CRFs suffer from low nutrient content, which limits their further application. To address this issue, this study synthesized a series of hierarchically porous MOFs, denoted as MIL-156(X), using sodium acetate as a modulator under hydrothermal conditions. These materials were subsequently loaded with urea and phosphate from aqueous solution to form MOFs-based CRFs (N-P-MIL-156(X)). Results indicate that MIL-156(X) retain microporous integrity while incorporating abundant mesopores. Increasing modulator content reduced particle size and average pore diameter but increased specific surface area and adsorption capacity for urea and phosphate. MIL-156-H (with a high modulator content addition) exhibited the highest adsorption capacity, conforming to Langmuir isotherm and pseudo-second-order kinetics. The adsorption mechanisms of urea and phosphate involved hydrogen bonding and the formation of Ca intra-spherical complexes, respectively. N-P-MIL-156-H contained 10.8% N and 16.3% P₂O₅, with sustained release durations exceeding 42 days (N) and 56 days (P₂O₅) in an aqueous solution. Pot trials demonstrated significantly higher nutrient use efficiency (N-44.8%, P₂O₅-16.56%) and a 12.22% yield increase compared to conventional fertilization (N-35.6%, P₂O₅-13.32%). Thus, N-P-MIL-156-H-based fertilization significantly promotes rice growth and N/P utilization efficiency, offering a promising strategy for developing controlled-release fertilizers and improving nutrient management. Full article

The prompt and reliable detection of NH₃ leakage at room temperature (RT) is considered important for safety assurance and sustainable production. Although chemiresistive NH₃ sensors feature low cost and structural simplicity, their practical application is hindered by high operating temperatures and inadequate selectivity. Metal–organic frameworks (MOFs) and their derivatives offer a promising approach to address these limitations. In this work, Ce-BDC precursors with tunable particle sizes and crystallinity were synthesized by adjusting the raw material concentration. Controlled pyrolysis yielded a series of CeO₂-C-X (X = 0.5, 1, 1.5, 2) materials with nanosized particles. Among them, the CeO₂-C-1 sensor delivered a high response of 82% toward NH₃ under 40% relative humidity at RT. Moreover, it possessed excellent selectivity, repeatability, and rapid response-recovery behavior compared with the other samples. CeO₂-C-1 also remained stable under varying oxygen and humidity conditions, demonstrating high applicability. The superior sensing properties may be attributed to its high specific surface area and optimized mesoporous structure, which facilitated efficient gas adsorption and reaction. These findings demonstrated that precise control of MOF precursors and the structure in CeO₂ nanomaterials was critical for achieving high-performance gas sensing and established Ce-MOF-derived CeO₂ as a promising sensing material for NH₃ detection at RT. Full article

This study investigates the hydrogen adsorption performance of activated carbon (AC) derived from rice husks and modified with magnesium and nickel salts. Adsorption isotherms were recorded at 25 °C and 50 °C up to 80 bar, simulating practical storage conditions. The unmodified AC exhibited the highest hydrogen uptake (0.62 wt% at 25 °C), attributed to its high surface area and dominant ultramicroporosity (<0.9 nm). Modifications with Mg and Ni reduced adsorption capacity, likely due to partial pore blockage and decreased surface functionality, as confirmed by FTIR, Raman, and XRD analyses. Despite this, all samples demonstrated stable cyclic adsorption–desorption behavior and consistent isotherm profiles. Hysteresis observed in the modified samples suggests capillary condensation within mesopores. Thermodynamic analysis confirmed the exothermic nature of hydrogen adsorption. Among the modified materials, ACM10 (Mg-modified) exhibited the best performance (0.54 wt%), highlighting the importance of optimizing the metal content. The obtained results indicate that the micropore size distribution and accessible surface functionality critically govern the hydrogen storage capacity, suggesting that unmodified AC is a promising candidate for low-temperature hydrogen storage systems. Full article

The controlled incorporation of halogens into carbon materials remains a challenge, particularly under mild and scalable conditions. In this work, we investigate the fixation of iodine on high-surface-area graphite (HSAG-100) using green solvents and moderate temperatures. Commercial HSAG was treated with iodine in aqueous and in organic media, with and without promoters, and characterized by XPS, LEIS, N₂ physisorption, TGA/TPD, and XRD. The results reveal that iodine contents up to ~0.6 at% can be achieved, with incorporation strongly influenced by solvent and reaction time. XPS and LEIS confirmed the presence of C–I bonds, while BET analysis showed only moderate decreases in surface area and unchanged mesopore size distribution. Thermogravimetric and TPD analyses demonstrated the high thermal stability of C–I species, and XRD patterns ruled out intercalation between graphene layers. Collectively, these findings demonstrate that iodine can be covalently anchored to HSAG under mild conditions, preserving the graphitic structure and generating stable edge functionalities, thus opening a route for the design of halogen-doped carbons for catalytic and electrochemical applications. Full article

The electrochemical performance of Li-ion batteries employing LiFePO₄ (LFP) cathodes supported by bio-sourced activated carbon derived from millet cob (MC) and water hyacinth (WH) were systematically investigated. Carbon activation was carried out using potassium hydroxide (KOH) at varying mass ratios of KOH to precursor material: 1:1, 2:1, and 5:1 for both WH and MC-derived carbon. The physical properties (X-ray diffraction patterns, BET surface area, micropore and mesopore volume, conductivity, etc.) and electrochemical performance (specific capacity, discharge at various current rates, electrochemical impedance measurement, etc.) were determined. Material characterization revealed that the activated carbon derived from MC exhibits an amorphous structure, whereas that obtained from WH is predominantly crystalline. High specific surface areas were achieved with activated carbons synthesized using a low KOH-to-carbon mass ratio (1:1), reaching 413.03 m²·g⁻¹ for WH and 216.34 m²·g⁻¹ for MC. However, larger average pore diameters were observed at higher activation ratios (5:1), measuring 8.38 nm for KOH/WH and 5.28 nm for KOH/MC. For both biomass-derived carbons, optimal electrical conductivity was obtained at a 2:1 activation ratio, with values of 14.7 × 10⁻³ S·cm⁻¹ for KOH/WH and 8.42 × 10⁻³ S·cm⁻¹ for KOH/MC. The electrochemical performance of coin cells based on cathodes composed of 85% LiFePO₄, 8% of these activated carbons, and 7% polyvinylidene fluoride (PVDF) as a binder, with lithium metal as the anode were studied. The LiFePO₄/C (LFP/C) cathodes exhibited specific capacities of up to 160 mAh·g⁻¹ at a current rate of C/12 and 110 mAh·g⁻¹ at 5C. Both LFP/MC and LFP/WH cathodes exhibit optimal energy density at specific values of pore size, pore volume, charge transfer resistance (R_ct), and diffusion coefficient (D_Li), reflecting a favorable balance between ionic transport, accessible surface area, and charge conduction. Maximum energy densities relative to active mass were recorded at 544 mWh·g⁻¹ for LFP/MC 2:1, 554 mWh·g⁻¹ for LFP/WH 2:1, and 568 mWh·g⁻¹ for the reference LFP/graphite system. These performance results demonstrate that the development of high-performing bio-sourced activated carbon depends on the optimization of various parameters, including chemical composition, specific surface area, pore volume and size distribution, as well as electrical conductivity. Full article

This paper presents the development and characteristics of geopolymer foams modified with paraffin-based phase change materials (PCMs) encapsulated in diatomite. The aim was to increase both the thermal insulation and heat storage capacity of the foams while maintaining sufficient mechanical strength for construction applications. Eleven variants of composites with different PCM fractions (5–10% by mass) and grain sizes (<1.6 mm to >2.5 mm) were synthesized and tested. The inclusion of PCM encapsulated in diatomite modified the porous structure: the total porosity increased from 6.6% in the reference sample to 19.6% for the 1.6–1.8 mm_10% wt. variant, with pore diameters ranging from ~4 to 280 µm. Thermal conductivity (λ) ranged between 0.090–0.129 W/m·K, with the lowest values observed for composites 2.0–2.5 mm_5–10% wt. (≈0.090–0.091 W/m·K), which also showed high thermal resistance (R ≈ 0.287–0.289 m²·K/W). The specific heat (Cp) increased from 1.28 kJ/kg·K (reference value) to a maximum value of 1.87 kJ/kg·K for the 2.0–2.5 mm_10% mass variant, confirming the effective energy storage capacity of PCM-modified foams. Mechanical tests showed compressive strength values in the range of 0.7–3.1 MPa. The best structural performance was obtained for the 1.6–1.8 mm_10% wt. variant (3.1 MPa), albeit with a higher λ (≈0.129 W/m·K), illustrating the classic trade-off between porosity-based insulation and mechanical strength. SEM microstructural analysis and mercury porosimetry confirmed the presence of mesopores, which determine both thermal and mechanical properties. The results show that medium-sized PCM fractions (1.6–2.0 mm) with moderate content (≈10% by weight) offer the most favorable compromise between insulation and strength, while thicker fractions (2.0–2.5 mm) maximize thermal energy storage capacity. These findings confirm the possibility of incorporating natural PCMs into geopolymer foams to create multifunctional materials for sustainable and energy-efficient building applications. A unique contribution to this work is the use of diatomite as a natural PCM carrier, ensuring stability, compatibility, and environmental friendliness compared to conventional encapsulation methods. Full article

Bimetallic mesoporous photocatalysts were synthesized via a wet impregnation method using SBA-15 as a support, and characterized by UV–visible diffuse reflectance spectroscopy, low-angle X-ray diffraction and N₂ physisorption. Among the tested materials, the Ti/Mn combination exhibited the highest photocatalytic activity in azo dye degradation. To understand this enhanced performance, catalysts with varying Mn loads and calcination ramps were evaluated. Additionally, experiments with radical scavengers (isopropanol, chloroform) and under N₂ insufflation were conducted to identify the active radical species. Catalysts prepared with low Mn content and higher calcination ramps showed the greatest activity, which significantly decreased with isopropanol, indicating hydroxyl radicals as the main reactive species. In contrast, samples with higher Mn content and quicker heating displayed reduced activity in the presence of chloroform, suggesting superoxide radical involvement. Spectroscopic analyses (XPS, UV–Vis DRS) revealed that increasing Mn load promotes the formation of Mn²⁺ over Mn⁴⁺ species and lowers the band gap energy. These findings highlight the direct correlation between synthesis parameters, surface composition and optical properties, providing a strategy for fine-tuning the performance of a photocatalyst. Full article

p-toluenesulfonic acid (pTSA) was used for the synthesis of porous silica xerogels while applying different synthesis conditions. Key parameters included acid concentration, drying temperature and the method of acid removal. The resulting organic–inorganic composites were investigated by nitrogen physisorption, X-ray powder diffraction (XRD), solid-state NMR and thermal analysis. The results demonstrated that both the drying temperature and quantity of the pTSA significantly influenced the pore structure of the xerogels. The utilization of such strong acids like pTSA yielded high surface area and pore volume, as well as narrow pore size distribution. Environmentally friendly template removal by solvent extraction produced materials with superior textural properties compared to traditional calcination, enabling the recovery and reuse of pTSA with over 95% efficiency. A selected mesoporous silica xerogel was modified by a simple two-step post-synthesis procedure with 1-(2-Hydroxyethyl) piperazine (HEP). High CO₂ adsorption capacity was determined for the HEP-modified material in dynamic conditions. The isosteric heat of adsorption revealed the stronger interaction between functional groups and CO₂ molecules. Total CO₂ desorption could be achieved at 60 °C. Leaching of the silica functional groups could not be detected even after four consecutive adsorption cycles. These findings provide valuable insights into the sustainable synthesis of tunable piperazine-modified mesoporous silica xerogels with potential applications in CO₂ capture. Full article

Mesoporous silica materials with well-organized architectures were synthesized using a series of Pluronic PE-type triblock copolymers (PE6800, PE9200, PE9400, PE10500) as structure-directing agents under acidic conditions. The study aimed to elucidate the impact of synthesis parameters—copolymer type, presence of a swelling agent, 1,3,5-trimethylbenzene, aging temperature, and silica precursor—on the structural, textural, and functional properties of the resulting mesocellular foam materials. Characterization by Nitrogen Adsorption/Desorption, Transmission Electron Microscopy, X-ray Diffraction, and Small-angle X-ray Scattering revealed that structural ordering and pore morphology are significantly influenced by the EO/PO ratio of the copolymers and the use of the expander. Materials synthesized with PE9400 and PE10500 in the presence of a swelling agent exhibited highly uniform bottle-shaped mesopores with increased surface area and pore volume. Thermal behavior studied via Differential Scanning Calorimetry indicated a correlation between pore size and melting point depression of confined water, consistent with the Gibbs–Thomson effect. Adsorption capacity and kinetics for methylene blue varied significantly with pore structure, with materials possessing narrow mesopores showing superior dye uptake, and materials with larger mesopores and open-pore architecture exhibiting faster adsorption rates. This work demonstrates the tunability of mesoporous silica structure through precise control of synthesis conditions and highlights its potential in applications involving adsorption and phase phenomena in confined pore systems. Full article