Search Results (636)

Zeolitic imidazolate frameworks (ZIFs) can provide fascinating stereo morphology and tunable metal active sites, which plays an important role in the synthesis of various catalytic materials. However, it is still a problem to make use of these advantages to design efficient hydrogen evolution reaction (HER) catalysts. Herein, we use covalent coordination strategy to synthesize bimetallic Co_xZn_1−x(2-MeIM)₂ precursors with regular dodecahedral structures for providing uniform active sites and stable carbon skeleton. Furthermore, the ratio of Co and Zn atoms was optimized to balance the electron density and give full play to the synergistic catalytic effect. And then, the subsequent high temperature annealing process is used to construct the amorphous carbon layer, which can improve the overall stability of the material. The gas phase phosphating process realizes the transformation from ZIF material to metal phosphide resulting in enhanced hydrogen evolution activity. Finally, the optimized amorphous nitrogen-doped carbon (NC)-coated Zinc-doped cobalt phosphide (Zn_0.17Co_0.83P@NC) requires only 237.60 mV to reach the current density of 10 mA cm⁻² in alkaline medium, which is 223.22 mV lower than that of CoP, and has a stability of up to 18 h. This work provides a reference for the rational design of efficient and stable compound electrocatalysts for alkaline hydrogen evolution based on the bimetallic ZIF as a precursor. Full article

There are many obstacles to the industrial application of CO₂ hydrogenation reduction technology, the most important of which is the high economic cost. The purpose of this study is to explore the interaction mechanism between the active component CuO-ZnO-Al₂O₃(CZA) and the zeolite carrier Zeolite Socony Mobil-5(ZSM-5), screen the simplified preparation method of catalysts with high catalytic performance, and further promote the industrial application of CO₂ hydrogenation reduction technology. In this study, the effects of the gas velocity of the feedstock, the reaction temperature, the content of acidic sites in the carrier, the filling amount of active component, and the mixing mode of the active component and the carrier on catalytic CO₂ hydrogenation reduction were investigated. The structure of the catalysts was analyzed by X-ray diffractometer (XRD), Brunauer-Emmett-Teller (BET), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and transmission electron microscopy (TEM). The catalyst surface properties were analyzed by X-ray photoelectron spectroscopy (XPS), ammonia temperature programmed desorption (NH₃-TPD), hydrogen temperature programed reduction (H₂-TPR) and other characterization methods. The research found that the grinding treatment led to the insertion of CZA between ZSM-5 zeolite particles in CZA@HZ5-20-GB, which was prepared via grinding both CZA and H-ZSM-5 with an Si/Al ratio of 20, inhibiting the action of strongly acidic sites in the zeolite, resulting in only CO and MeOH in the catalytic products, with no Dimethyl Ether (DME) generation. Full article

Green nanotechnology offers a sustainable and eco-friendly approach for nanoframework synthesis. The present study intended to synthesize a novel eco-friendly encapsulated Zeolitic Imidazolate Framework-8 (ZIF-8) in a one-pot method using metabolites from the mangrove plant Conocarpus erectus (CE). Gas Chromatography–Mass Spectrometry (GC-MS) analysis of the extract revealed the presence of important bioactive metabolites. The synthesized material was evaluated by UV-Vis spectroscopy, X-ray diffraction (XRD), particle size analysis (PSA), zeta potential measurement, high-resolution transmission electron microscopy (HR-TEM), and Fourier transform infrared (FT-IR) spectroscopy studies. The environment-friendly mangrove metabolites aided by Zeolitic Imidazolate Framework-8 was found to be crystalline, rhombic dodecahedron structured, and size dispersed without agglomeration. The nanomaterial possessed a broad antimicrobial effect on drug-resistant microorganisms, including Candida krusei, Escherichia coli, Streptococcus Sp., Staphylococcus aureus, Enterococcus Sp., Pseudomonas aeruginosa, Klebsiella pneumoniae, C. propicalis, and C. albicans. Further, its cytotoxicity against MDA-MB-231 cells was found to be efficient. The morphological alterations exhibited by the antiproliferative impact on the breast cancer cell line were detected using DAPI and AO/EB staining. Therefore, ZIF-8 encapsulated mangrove metabolites could serve as an effective biomaterial with biomedical properties in the future. Full article

The local segmental mobility of polymer chains in polydimethylsiloxane (PDMS) plays a critical role in determining the material’s behaviour. Incorporation of zeolite particles can modify these local dynamics, which is crucial as they affect the overall performance of the resulting composite material with potential for various industrial applications. The aim of this study was to investigate the influence of zeolite addition on the local dynamic behaviour of PDMS chain segments in PDMS–zeolite composites. To investigate the effect of zeolite morphology and loading on the segmental dynamics and phase behaviour of PDMS, Zeolite A (with cubic and spherical morphologies) and Zeolite X were incorporated into the PDMS matrix at 20, 30, and 40 wt%. The electron spin resonance (ESR)-spin probe method was used to study molecular dynamics, while the thermal behaviour was analysed using differential scanning calorimetry (DSC). ESR results revealed that the presence of zeolites increases the isothermal crystallisation rate affecting segmental mobility in the amorphous phase below the crystallisation temperature. This effect was found to depend more strongly on zeolite morphology than on filler content. DSC measurements showed no change in glass transition temperature with the addition of zeolite; however, shifts in cold crystallisation and melting behaviour were observed, indicating changes in crystal structure and its degree of perfection. These findings suggest that zeolites act as heterogeneous nucleation agents, with their structural properties playing a critical role in the crystallisation behaviour of PDMS. Full article

The interfacial properties in carbon fiber (CF)-reinforced polymer composites are substantially limited by the chemically inactive and smooth CF surfaces. In this study, zeolitic imidazolate framework 90 (ZIF90) was chemically grafted onto CF surfaces via polyethyleneimine (PEI) as a coupling agent to construct a hierarchical reinforcement interface in CF/epoxy composite. The successful synthesis of CF grafted with PEI and ZIF90 (CF-PEI-ZIF90) was systematically characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The incorporation of ZIF90 nanocrystals and PEI molecules into CF surfaces effectively improved interfacial adhesion through mechanical interlocking and chemical interactions, thereby optimizing stress transfer efficiency at the fiber–matrix interface and improving the interfacial properties of the composite. Additionally, the resultant CF-PEI-ZIF90/epoxy composite demonstrated significant mechanical enhancement, with the tensile and bending strengths increasing by 33.5% and 21.4%, respectively, compared to unmodified CF/epoxy composites. This work provides a novel strategy for enhancing the interfacial performance of CF composites by leveraging the unique properties of metal-organic frameworks, which is critical for advancing high-performance structural materials in aerospace and automotive applications. Full article

The valorization of volcanic ash as a raw material for advanced functional materials offers dual benefits for both the environment and technology. Firstly, it diverts waste from landfills, thereby reducing the environmental footprint of volcanic deposits. Secondly, it contributes to the circular economy by transforming an abundant natural residue into a high-value product. In this study, zeolites were synthesized from the ash of the Ubinas volcano via the hydrothermal method in an alkaline medium. A systematic investigation was conducted to ascertain the influence of NaOH concentration and reaction temperature on synthesis efficiency and final material properties. The crystalline phases and morphology of the products were characterized using Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM), while textural and thermal properties were evaluated through the Brunauer–Emmett–Teller (BET) method and Thermogravimetric Analysis (TGA). The results revealed that both temperature and NaOH concentration significantly affected the physicochemical properties of the zeolites. Four zeolite types were obtained; among them, Zeolite Z4 (synthesized with 3 M NaOH at 150 °C) exhibited the highest adsorption capacity, with a specific surface area of 35.60 m²/g, while Zeolite Z1 (synthesized at 120 °C with 1.5 M NaOH and 27.85 m²/g) displayed superior thermal stability and crystallinity. These variations in thermal and textural properties were reflected in the catalytic pyrolysis performance of polypropylene (PP). Zeolite Z3 (synthesized at 150 °C with 1.5 M NaOH) achieved the highest gaseous product yield (80.2%), despite lacking the expected zeolitic crystalline phases. In contrast, Zeolite Z2 (synthesized at 120 °C with 3 M NaOH) yielded 57.7% gaseous products and stood out for its predominant analcime phase, characteristic of zeolitic materials. In summary, this study demonstrates that volcanic ash-derived zeolites not only enhance synthesis efficiency and functional performance but also represent a sustainable strategy for waste valorization, closing material loops and enabling the recovery of high-calorific gaseous products from plastic waste. Full article

The widespread presence of bisphenol A (BPA), a persistent endocrine-disrupting pollutant, in aquatic environments poses significant ecological and health risks, necessitating its effective removal. However, conventional remediation technologies are often hampered by catalysts with narrow pH adaptability and poor stability. In this study, a novel catalyst, Zeolite-supported Cu₃Mn-layered double hydroxide (LDH), was fabricated using the co-precipitation method. The synthesized catalyst was applied to activate peroxymonosulfate (PMS), effectively enabling decomposition of BPA by advanced oxidation processes. The composite material was characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM), which confirmed the successful synthesis of the zeolite-supported Cu₃Mn-LDH. The catalyst exhibited high activity in both neutral and strongly alkaline environments, achieving complete degradation of 10 mg⋅L⁻¹ bisphenol A (BPA) within 40 min and a 98% total organic carbon (TOC) removal rate when both the PMS and catalyst were dosed at 0.15 g⋅L⁻¹. Singlet oxygen was detected as the primary reactive species responsible for BPA degradation, as verified by quenching experiments and EPR analysis, which also identified the presence of sulfate (SO₄^•−), hydroxyl (•OH), and superoxide (•O₂⁻) radicals. The catalyst exhibited excellent reusability, maintaining high catalytic efficiency over two consecutive cycles with minimal performance loss. Gas chromatography-mass spectrometry (GC-MS) analysis revealed five intermediate products, enabling the proposal of potential BPA degradation pathways. This work not only presents a novel synthetic approach for zeolite-supported LDH composites, but also offers a promising strategy for the efficient removal of BPA from aqueous systems through AOPs. Full article

Coffee drying in humid regions is frequently hindered by high rainfall and elevated relative humidity during peak harvest, prolonging drying times and risking microbial spoilage and quality deterioration. This study introduces a novel framework in which low-temperature drying is reframed as a gas–solid dehydration reaction, promoted by a catalyst analog represented by regenerable desiccants integrated into the inlet air stream to lower the humidity ratio (ΔY) and intensify the evaporation driving force. Two adsorbents, silica gel type A and zeolite 13X, were evaluated using a coupled reactor model linking fixed-bed adsorption kinetics with tensorial heat–mass transport in a 70 kg batch of parchment coffee arranged in a 0.20 m thick bed. Drying simulations from 53% to 12% (wb) at 40, 45, and 50 °C showed time reductions of 35–37% with silica gel and 44–57% with zeolite, yielding kinetic promotion factors of up to 2.3× relative to the control. Breakthrough analysis supported a dual-bed alternation strategy, with regeneration at ≤130 °C for silica and moderately higher for zeolite. A nomograph was developed to scale desiccant requirements across airflow and ΔY targets. These results confirm the feasibility and scalability of desiccant-assisted drying, providing a modular intensification pathway for farm-scale coffee processing. Full article

Oxygenated volatile organic compounds are key precursors of secondary photochemical pollutants. To enhance their removal, NaY–zeolite was modified with nano-sized metals (Fe, Ti, Si, or Ce) using impregnation and sol–gel methods. Dynamic adsorption experiments were conducted to evaluate the adsorption of ethanol, acetaldehyde, and ethyl acetate under various condition modifications, including of the impregnation concentration, treatment time, and calcination temperature. The structural and surface properties of the modified zeolites were characterized by N₂ adsorption–desorption isotherm, X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR) analyses. The results indicated that the metal-loaded zeolites exhibited significantly higher adsorption capacities than the unmodified NaY–zeolite. Among them, silicon-modified zeolite showed the best performance, with its adsorption capacities for ethanol, acetaldehyde, and ethyl acetate increasing from 32.4, 72.4, and 123.0 mg·g⁻¹ to 49.82, 88.94, and 207.02 mg·g⁻¹, corresponding to improvements of 37%, 23%, and 70%. The optimal modification conditions involved the use of silicon as the modifier with a 7% impregnation concentration, a 12 h impregnation time, and calcination at 350 °C; the zeolite modified under these conditions was characterized by a good adsorption capacity and low preparation cost. This study suggests newly designed adsorber materials suitable for highly efficient treatment of oxygenated volatile organic compounds. Full article

Clay minerals and other flocculants are used to mitigate the effects of some species that produce harmful algal blooms due to their physical and chemical characteristics. In this study, we applied calcium bentonite clay (Bca) and zeolite (Ze) to flocculate and remove cells of the dinoflagellate Gymnodinium catenatum (Graham), a producer of paralyzing toxins. The flocculants were characterized by scanning electron microscopy (SEM) in combination with an energy-dispersive X-ray spectroscopy (EDS) microanalysis system. During experiments, Bca and Ze were suspended in distilled water, deionized water, and seawater at concentrations of 0.25, 0.5, 1.0, 1.5, 2.0, 2.5, and 4.0 gL⁻¹. The percentage of removal efficiency (RE%) of biomass indicators of G. catenatum was calculated. The cell number and concentration of chlorophyll a and peridinin were analyzed using high-performance liquid chromatography (HPLC-UV and HPLC-DAD). The external effects on cells of G. catenatum were recorded. As a result, the maximum RE% of Bca was 79% with respect to the total number of cells, chlorophyll a was 69% and peridinin of 73%. The RE% of Ze was less than 40%. In the matrix of sedimented Bca, malformation of cells was observed, inhibiting their swimming, as well as death and rupture of cells with temporary cyst formation after 72 h. We conclude that Bca, suspended in deionized and distilled water, was more efficient in flocculating cells of G. catenatum. Full article

This study evaluates the impact of mineralogy, elemental composition, and reaction pathways on hydrogen (H₂) generation in seven ultramafic and mafic (basaltic) rocks. Experiments were conducted under typical low-temperature hydrothermal conditions (150 °C) and captured early and evolving stages of fluid–rock interaction. Pre- and post-interactions, the solid phase was analyzed using X-ray Diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS), while Inductively Coupled Plasma Mass Spectrometry (ICP-MS) was used to determine the composition of the aqueous fluids. Results show that not all geologic H₂-generating reactions involving ultramafic and mafic rocks result in the formation of serpentine, brucite, or magnetite. Our observations suggest that while mineral transformation is significant and may be the predominant mechanism, there is also the contribution of surface-mediated electron transfer and redox cycling processes. The outcome suggests continuous H₂ production beyond mineral phase changes, indicating active reaction pathways. Particularly, in addition to transition metal sites, some ultramafic rock minerals may promote redox reactions, thereby facilitating ongoing H₂ production beyond their direct hydration. Fluid–rock interactions also regenerate reactive surfaces, such as clinochlore, zeolite, and augite, enabling sustained H₂ production, even without serpentine formation. Variation in reaction rates depends on mineralogy and reaction kinetics rather than being solely controlled by Fe oxidation states. These findings suggest that ultramafic and mafic rocks may serve as dynamic, self-sustaining systems for generating H₂. The potential involvement of transition metal sites (e.g., Ni, Mo, Mn, Cr, Cu) within the rock matrix may accelerate H₂ production, requiring further investigation. This perspective shifts the focus from serpentine formation as the primary driver of H₂ production to a more complex mechanism where mineral surfaces play a significant role. Understanding these processes will be valuable for refining experimental approaches, improving kinetic models of H₂ generation, and informing the site selection and design of engineered H₂ generation systems in ultramafic and mafic formations. Full article

Mine effluents represent a serious environmental problem on a global scale. Therefore, the effective treatment of this water is a serious issue in the scientific field. The adsorption process seems to be one of the attractive methods, especially due to the simplicity of design, affordability or high efficiency. The latest scientific knowledge has shown that the use of waste and natural adsorbents is economical and effective. This study aimed to evaluate the efficiency of the adsorption process of natural and waste materials—zeolite, bentonite and fly ash—under the influence of temperature and modification of these adsorbents. The novelty of this study resides in an adjustment of the modification method of adsorbents compared to previous research: thermal–alkaline treatment versus hydrothermal one. Another novelty is the use of modified fly ash from biomass combustion as an adsorbent in comparison with the previously used fly ash from coal combustion. The modification of the adsorbents made the adsorption process more effective at all experimental concentrations. The characterisation of adsorbent samples was performed using X-ray diffraction (XRD). The parameters of the adsorption isotherms, Langmuir, Freundlich and Temkin, were estimated by nonlinear regression analysis. The adsorption capacity of Cu(II) of fly ash was comparable to natural adsorbents. Adsorption processes were better described by pseudo-second-order kinetics. At the end of this study, the suitability of using the adsorbents to reduce the concentration of Cu(II) in neutral mine effluents was observed in the following order at 30 °C: unmodified fly ash > modified bentonite > unmodified zeolite. At the temperatures of 20 °C and 10 °C, the same trend of the suitability of adsorbents use was confirmed: modified bentonite > modified zeolite > modified fly ash. The practical applicability of this study lies in the expansion of knowledge in the field of adsorption processes and in the improvement of waste management efficiency of heating plants not only in Slovakia, but also globally. Full article

The zeolite structure, with its precisely distinct pores, settled cages, and adsorption sites, enables the formation and stabilization of isolated metal centers. These well-defined structures make metal-loaded zeolites promising catalysts. Three different β zeolites were synthesized by an aqueous ion-exchange procedure, firstly with cobalt (Co), and secondly with zinc (Zn), cerium (Ce), and copper (Cu), to make three bimetallic CoZn/β, CoCe/β, and CoCu/β zeolites, respectively. X-ray powder diffraction analysis, Fourier transform infrared spectroscopy, scanning electron microscopy with energy dispersive spectroscopy, and low-temperature nitrogen adsorption analysis revealed the structural, morphological, and surface properties of the studied materials, while optical properties were investigated by UV-Vis diffuse reflectance spectroscopy. The lowest onset potential of 1.67 V was obtained for both CoZn/β and CoCe/β, while the somewhat positive value of 1.70 V was observed for CoCu/β. CoZn/β exhibited the lowest value of Tafel slope of 89 mV dec^−1, while slightly higher values of 109 and 113 mV dec⁻¹ were calculated for CoCe/β and CoCu/β during ORR, respectively. CoZn/β showed four-electron pathways of ORR, CoCu/β showed a mixed ORR mechanism, while CoCe/β offered two-electron pathways of ORR. All presented results established that CoZn/β had the highest OER/ORR activity, followed by CoCu/β, while CoCe/β had the lowest activity detected. Full article

According to the international standard ISO 14687:2019 for hydrogen fuel quality, the maximum allowable concentration of water in hydrogen for use in refueling stations and storage systems must not exceed 5 µmol/mol. Therefore, an adsorption purification process following the electrolyzer is necessary. This study numerically investigates the adsorption of water and the corresponding water loading on zeolite 13X BFK, based on the mass flows entering the adsorption column from three 5 MW electrolyzers coupled to a 15 MW offshore wind turbine. As the mass flow is influenced by wind speed, a direct comparison between realistic wind speeds and adsorption loading is presented. The presented numerical discretization of the model also accounts for perturbations in wind speed and, consequently, mass flows. In addition, adsorption isobars were measured for water on zeolite 13X BFK within the required pressure and temperature range. The measured data was utilized to fit parameters to the Langmuir–Freundlich isotherm. Full article

The durability of construction and building materials under sulphate environments is an important indicator to evaluate their service life. In this study, the physical and mechanical behaviours of wood-ash-based alkali-activated materials (AAMs) incorporating coal fly ash, metakaolin, natural zeolite, and calcined phosphogypsum were assessed before and after being subjected to sodium sulphate corrosion cycles via the compressive strength, mass, and volume changes. The microstructure, elemental composition, and phase identification were further analysed using X-Ray Diffraction(XRD) and scanning electron microscope(SEM). The results show that the exposure to sulphate solution caused decalcification and dealumination of hydrates, releasing calcium and aluminium to react with sulphate and forming expansive erosion products, ettringite and gypsum. This contributed to the microstructural damage, leading to mass change, volume expansion, and compressive strength loss of 7.33, 1.29, and 60.42%. The introduction of binary aluminosilicate precursors enhanced the sulphate resistance by forming a well-bonded microstructure consisting of calcium (aluminate) silicate hydrate and sodium aluminate silicate hydrate, with the compressive strength loss decreasing up to 18.60%. The co-usage of calcined phosphogypsum deteriorated the mechanical properties of AAMs but significantly improved the sulphate resistance. The sodium sulphate environment facilitated anhydrate hydration, generating more sulphate hydrates and hemigypsums that co-existed with erosion products, forming a compact microstructure and improving the compressive strength by twofold. Full article