Search Results (24)

This study focuses on the exchange of mono- and divalent metal cations in FAU-type zeolite and their behavior in gas-phase CO₂ adsorption measurements and liquid-phase methylene blue (MB) adsorption in the absence of oxidizing agents under dark conditions. Firstly, zeolites exchanged with different cations were characterized by several techniques, such as XRD, SEM, XRF, XPS, and N₂ adsorption–desorption, to reveal the impact of the cations on the zeolite texture and structure. The adsorption studies revealed a positive effect of cation exchange on the adsorption capacity of the zeolite, particularly for silver-loaded FAU zeolite. In liquid-phase experiments, Ag-Y zeolite also demonstrated the highest MB removal, with a value of 79 mg/g. Kinetic studies highlighted that Ag-Y could reach the MB adsorption equilibrium within 1 h, with its highest rate of adsorption occurring during the first 5 min. In gas-phase adsorption studies, the highest CO₂ adsorption capacity was also achieved over Ag-Y, yielding 10.4 µmol/m² of CO₂ captured. Full article

Radon (Rn) is a hazardous radioactive gas that poses significant health risks in enclosed indoor environments. This study investigates the potential of silver-exchanged clinoptilolite-rich natural zeolite (NZ-Ag⁺) for the removal of Rn from air. Natural zeolite (NZ) was thermally treated and further modified to enhance its adsorption characteristics. The thermally treated NZ (200 °C) was first exchanged in Na⁺ form, since Na⁺ is more easily exchanged in clinoptilolite with hydrated Ag⁺ ions than the other exchangeable cations. The modification with Ag⁺ was carried out at room temperature using ultrasonic processing to obtain (NZ-Ag⁺). The materials were characterized in terms of chemical composition, cation exchange capacity, mineralogy, total surface area, pore volume, and thermal behavior. Rn adsorption experiments were performed using a closed-circuit system, and the efficiency of NZ-Ag⁺ was compared with that of NZ. The results indicate that NZ-Ag⁺ exhibits superior Rn adsorption capacity, achieving up to 50% higher retention efficiency compared to NZ. The improved performance is attributed to enhanced adsorption facilitated by silver ion clusters interacting with radon atoms. These results suggest that silver-exchanged zeolite represents a promising material for radon mitigation in air filtration systems, with potential applications in residential and occupational settings. Full article

The increasing presence of pollutants, including pharmaceuticals and pesticides, in water resources necessitates the development of effective remediation technologies. Zeolites are promising agents for pollutant removal due to their high surface area, ion-exchange capacity, natural abundance, and diverse tailorable porous structures. This review focuses on the efficient application of modified zeolites and mesoporous materials as photocatalysts and adsorbents for removing contaminants from water bodies. The adsorption and photodegradation of pesticides and selected non-steroidal anti-inflammatory drugs and antibiotics on various zeolites reveal optimal adsorption and degradation conditions for each pollutant. In most reported studies, higher SiO₂/Al₂O₃ ratio zeolites exhibited improved adsorption, and thus photodegradation activities, due to increased hydrophobicity and lower negative charge. For example, SBA-15 demonstrated high efficiency in removing diclofenac, ibuprofen, and ketoprofen from water in acidic conditions. Metal doped into the zeolite framework was found to be a very active catalyst for the photodegradation of organic pollutants, including pesticides, pharmaceuticals, and industrial wastes. It is shown that the photocatalytic activity depends on the zeolite-type, metal dopant, metal content, zeolite pore structure, and the energy of the irradiation source. Faujasite-type Y zeolites combined with ozone achieved up to 95% micropollutant degradation. Bentonite modified with cellulosic biopolymers effectively removed pesticides such as atrazine and chlorpyrifos, while titanium and/or silver-doped zeolites showed strong catalytic activity in degrading carbamates, highlighting their environmental application potential. Full article

Objectives: The antimicrobial, oxidative activities, and ecotoxicity of synthesized silver-loaded zeolites (X and ZSM-5(MFI), Si-to-Al ratios 12 and 25) were studied, linking antimicrobial properties to material structure and released active silver species. Methods: The materials were characterized by SEM, EDX, TEM, and XRPD. All materials, with a silver content of 1–3%wt for the Ss and about 35%wt for the X-zeolites, were tested against Escherichia coli and Staphylococcus aureus. Redox activity was studied in physiological (pH 7.4/37 °C) and optimal (pH 8.5/37 °C) conditions in chemiluminescent model systems. In the ecotoxicity tests, we used Daphnia magna. Results: A proportional correlation was observed between the bactericidal effect of and the silver content in the zeolites. AgX with a Si/Al ratio of ~1.23 and 35% silver showed a higher antimicrobial efficiency, particularly against Gram-negative E. coli versus Gram-positive S. aureus. The concentration thresholds were as follows: AgXas had a bactericidal effect at 0.003 g/L⁻¹, with an MIC at 0.0015 m/L⁻¹ for E. coli; SA25-Ag, AgXcl, AgXrc had a bactericidal effect at 2.5 g/L⁻¹. The bacteria were more resilient than Daphnia magna, which showed a 90–100% lethality at Ag–zeolite concentrations of 0.00625 to 0.0125 g/L⁻¹. AgXas and AgXrc demonstrated strong reactive oxygen species generation at both the physiological and optimal pH, explaining their bactericidal effects. In general, the tested materials showed an inhibition of the generated reactive oxygen species depending on the model system and conditions. Conclusions: The silver species leached from the new materials explain their higher oxidation and bactericidal activity. While suitable for stringently controlled biological applications, their release into the environment, in concentrations higher than 0.01g/L⁻¹, should be avoided. Full article

Environmentally friendly powder coatings which have the advantages of being VOC-free, low-cost, and high-efficiency with a high recovery rate have been attracting increasing research attention. The introduction of antibacterial agents into the powder coatings endows them with a capacity to kill bacteria and viruses on the surface of objects; additionally, this enables them to inhibit the indirect transmission of pathogenic microorganisms. Silver, possessing broad-spectrum, strong, and stable antibacterial properties, is considered to be a promising antibacterial material for use in coating applications. Carrier materials for active silver play an important role in its activity and stability. However, there is a lack of systematic studies on the effects of different types of carriers in such coating systems, especially in green powder coating systems. In this paper, we investigated two types of carriers for active silver agents: zeolite, i.e., Linde type A (LTA) zeolite and Y-type zeolite; clay-based materials, i.e., montmorillonite and vermiculite. All the agents showed high antibacterial activity, with antibacterial rates of over 99% as compared to commercial agents. Among the four agents, the Ag-LTA zeolite antimicrobial agent showed a reduction rate of over 99.99%; additionally, it maintained a reduction rate of 99% after seven washing cycles. Thus, this agent was demonstrated to have the highest effectiveness and high durability; these features can be attributed to the high silver content and small particle size. The LTA zeolite also provides a protective effect for silver ions, protecting them from reduction, due to the restriction of elemental silver formation within the confined interior space of the α-cage structure. The Y-type zeolite antimicrobial agent exhibited a slightly lower antimicrobial performance due to its higher silicon-to-aluminum ratio and its lower cation exchange capacity. Comparatively, antimicrobial agents utilizing clay-based carriers have lower cation exchange capacity, resulting in poorer antimicrobial effectiveness than zeolite carriers. In addition, silver loaded on clay-based materials is prone to detach from the carrier and undergo a reduction reaction, making the coating yellowish in color. This study first provides information on the roles of different types of carriers in powder coating systems; then, this information guides the selection of carriers for active silver for the development of efficient antimicrobial agents and coatings. Full article

The removal of hydrogen sulfide from natural gas and other gases such as biogas, refinery gases, and coal gas is required because it is toxic and corrosive, even in traces. Zeolites are widely used in the removal of H₂S from the abovementioned gases. In this work, we prepared an Ag-exchanged 13X molecular sieve by using different concentrations of AgNO₃ to increase its adsorption properties. XRD, SEM, and BET techniques were used to characterize samples. To determine the adsorption properties of each of the samples, a laboratory setup with a fixed-bed adsorber was utilized. The adsorption capacity of modified 13X increased when the molar concentration of AgNO₃ increased from 0.02 M to 0.05 M. However, the breakthrough time was attained quicker at a high molar concentration of 0.1 M AgNO₃, indicating a low adsorption capacity. When compared to unmodified 13X, the adsorption capacity of AgII-13X increased by about 50 times. The results of this study suggest that the silver-modified 13X molecular sieve is highly effective at extracting H₂S from natural gas. Full article

Zeolites and zeolitic imidazolate frameworks (ZIFs) are crystalline aluminosilicates with porous structure, which are closely linked with nanomaterials. They are characterized by enhanced ion exchange capacity, physical–chemical stability, thermal stability and biocompatibility, making them a promising material for dental applications. This review aimed to provide an overview of the application of zeolites and ZIFs in dentistry. The common zeolite compounds for dental application include silver zeolite, zinc zeolite, calcium zeolite and strontium zeolite. The common ZIFs for dental application include ZIF-8 and ZIF-67. Zeolites and ZIFs have been employed in various areas of dentistry, such as restorative dentistry, endodontics, prosthodontics, implantology, periodontics, orthodontics and oral surgery. In restorative dentistry, zeolites and ZIFs are used as antimicrobial additives in dental adhesives and restorative materials. In endodontics, zeolites are used in root-end fillings, root canal irritants, root canal sealers and bone matrix scaffolds for peri-apical diseases. In prosthodontics, zeolites can be incorporated into denture bases, tissue conditioners, soft denture liners and dental prostheses. In implantology, zeolites and ZIFs are applied in dental implants, bone graft materials, bone adhesive hydrogels, drug delivery systems and electrospinning. In periodontics, zeolites can be applied as antibacterial agents for deep periodontal pockets, while ZIFs can be embedded in guided tissue regeneration membranes and guided bone regeneration membranes. In orthodontics, zeolites can be applied in orthodontic appliances. Additionally, for oral surgery, zeolites can be used in oral cancer diagnostic marker membranes, maxillofacial prosthesis silicone elastomer and tooth extraction medicines, while ZIFs can be incorporated to osteogenic glue or used as a carrier for antitumour drugs. In summary, zeolites have a broad application in dentistry and are receiving more attention from clinicians and researchers. Full article

The integration of hydroxyapatite (HA) with broad-spectrum bactericidal nano-silver within biopolymer-based bone scaffolds not only promotes new bone growth, but also effectively prevents bacterial infections. However, there are problems such as a poor interface compatibility and easy agglomeration. In this project, zeolitic imidazolate frameworks (ZIF-8) were grown in situ on nano-HA to construct a core–shell structure, and silver was loaded into the ZIF-8 shell through ion exchange. Finally, the core–shell structure (HA@Ag) was composited with polylactic acid (PLLA) to prepare bone scaffolds. In this case, the metal zinc ions of ZIF-8 could form ionic bonds with the phosphate groups of HA by replacing calcium ions, and the imidazole ligands of ZIF-8 could form hydrogen bonds with the carboxyl groups of the PLLA, thus enhancing the interface compatibility between the biopolymers and ceramics. Additionally, the frame structure of MOFs enabled controlling the release of silver ions to achieve a long-term antibacterial performance. The test results showed that the HA@Ag nanoparticles endowed the scaffold with good antibacterial and osteogenic activity. Significantly, the HA@Ag naoaprticle exhibited a good interfacial compatibility with the PLLA matrix and could be relatively evenly dispersed within the matrix. Moreover, the HA@ZIF-8 also effectively enhanced the mechanical strength and degradation rate of the PLLA scaffold. Full article

This study presents the synthesis of zeolites derived from coal fly ash (CFA) using the fusion-assisted alkaline hydrothermal method. The zeolites were synthesized by combining CFA and NaOH at a molar ratio of 1:1.2 under fusion temperatures of 500, 600, and 700 °C. Subsequently, the obtained zeolites were subjected to further modifications through the incorporation of magnetic (Fe₃O₄) and silver (Ag⁰) nanoparticles (NPs). The Fe₃O₄ NPs were introduced through co-precipitation of Fe(NO₃)₂ and FeCl₃ at a molar ratio of 1:1, followed by thermal curing at 120 °C. On the other hand, the Ag⁰ NPs were incorporated via ion exchange of Na⁺ with Ag⁺ and subsequent reduction using NaBH₄. The synthesized porous materials exhibited the formation of zeolites, specifically analcime and sodalite, as confirmed by X-ray diffraction (XRD) analysis. Additionally, the presence of Fe₃O₄ and Ag⁰ NPs was also confirmed by XRD analysis. The elemental composition analysis of the synthesized nanocomposites further validated the successful formation of Fe₃O₄ and Ag⁰ NPs. Nitrogen porosimetric analysis revealed the formation of a microporous structure, with the BET surface area of the zeolites and nanocomposites ranging from 48.6 to 128.7 m²/g and pore sizes ranging from 0.6 to 4.8 nm. The porosimetric characteristics of the zeolites exhibited noticeable changes after the modification process, which can be attributed to the impregnation of Fe₃O₄ and Ag⁰ NPs. The findings of this research demonstrate the effectiveness of the fusion-assisted method in producing synthetic zeolites and nanocomposites derived from CFA. The resulting composites were evaluated for their potential application in the removal of mercury ions from aqueous solutions. Among the samples tested, the composite containing Ag⁰ NPs exhibited the highest adsorption capacity, reaching 107.4 mg of Hg²⁺ per gram of composite. The composites modified with Fe₃O₄ NPs and Ag/Fe₃O₄ nanocomposites displayed adsorption capacities of 68.4 mg/g and 71.4 mg/g, respectively. Full article

FAU-type zeolite NaX was successfully prepared using hydrothermal synthesis at 90 °C for 6 h. The Mn- and Cu-ion-exchanged NaX zeolites were obtained. After the ion exchange, the zeolite powders were thermally treated at 300 °C. As well as Ag-ion-exchanged zeolite, NaX and zeolite were impregnated with two types of Ag nanoparticle dispersions: citrate surface-stabilized (Cit@Ag NPs) and polymer-stabilized (PVP@Ag) nanoparticles. Silver nanoparticles were synthesized using the electrochemical reduction method. The changes in the phase and chemical composition and structure of the obtained zeolite powders before and after ion exchange or impregnation were investigated by PXRD analysis, FTIR spectroscopy, and XRF analysis. The results show that Mn, Cu-exchanged NaX, and that impregnated with Ag demonstrated catalytic abilities towards ozone decomposition in comparison with pure zeolite (non-catalytic activity). Full article

Silver nanoclusters (Ag NCs) are nanoscale aggregates that possess molecular-like discrete energy levels, resulting in electronic configuration-dependent tunable luminescence spanning the entire visible range. Benefiting from the efficient ion exchange capacity, nanometer dimensional cages, and high thermal and chemical stabilities, zeolites have been employed as desirable inorganic matrices to disperse and stabilize Ag NCs. This paper reviewed the recent research progresses on the luminescence properties, spectral manipulation, as well as the theoretical modelling of electronic structure and optical transition of Ag NCs confined inside various zeolites with different topology structures. Furthermore, potential applications of the zeolite-encaged luminescent Ag NCs in lighting, gas monitoring and sensing were presented. This review concludes with a brief comment on the possible future directions in the study of zeolite-encaged luminescent Ag NCs. Full article

Nano-silver is characterized by broad-spectral, strong and stable antibacterial properties, which make it a promising material in coating applications. However, the efficiency of nano-silver is generally low in the coating of films. Here, we developed a series of highly active and durable silver ions–nano-silver antimicrobial agents for powder coatings. To optimize antimicrobial activity and durability, two different nano-silver generation methods, i.e., in situ and ex situ methods combined with different carrier materials, i.e., zeolite with high ion-exchange ability and montmorillonite of layered structure were adopted and investigated. All four antibacterial additives show high activity with a reduction rate of over 99.99% and R value of over 5. The ex situ generated nano-silver antibacterial agents with both carriers exhibit higher activity in the initial antibacterial property and antibacterial durability that the coating films are able to maintain over 99% antimicrobial reduction after 20 cycles (1200 times) of soap solution wiping. They also show a lower yellowish color difference of less than three compared to the films with in situ generation method. The one with montmorillonite as carrier shows the stronger antibacterial property with an R value of 5.88 and slightly better film appearance of lower color difference, smaller reduction in gloss and increase in haze as compared to zeolite carrier due to the layered structure. Full article

The recovery and immobilization of metals from wastewater often occurs in an acidic environment that destroys the structure of adsorbents such as zeolites, which are porous crystalline aluminosilicates. The influence of hydrochloric acid solutions on the structure and properties of two natural mixtures of heulandite (HEU) and chabazite (CHA)—tuff from the Georgian Dzegvi-Tedzami deposit (HEU/CHA ≈ 8) and rock from the Kazakhstani deposit Chankanay (HEU/CHA≈1)—was studied by the X-ray energy dispersion spectra and diffraction patterns, as well as by adsorption of water, benzene, and nitrogen methods. It was found that acid-mediated dealumination, decationization, dissolution, and changes in systems of micro- and mesopores depend on the nature and chemical composition of the initial zeolites. It is concluded that, under the influence of acid, (i) zeolite micropores become accessible to relatively large molecules and ions, and the surface area of the adsorbent increases; (ii) the volume of mesopores decreases, and pores with a diameter of less than 4 nm become predominant; (iii) in terms of the degree of dealumination and dissolution rate, Kazakhstani zeolite is more acid-resistant than Georgian heulandite; and (iv) Kazakhstani zeolite retains a high ion-exchange capacity in an acidic environment, while Georgian heulandite, treated with dilute hydrochloric acid solutions, uptakes relatively high amounts of valuable silver, copper, and zinc. Full article

In the present work, various experimental and theoretical methods were combined to study in detail the modifying effect of differences in the order of deposition of components on the state of silver in bimetallic iron–silver samples based on mordenite. In each of the silver-containing samples, the formation of large (≥2 nm in diameter) varieties of silver was observed, which differed from the varieties in the other samples, and in varying degrees. The formation of large Ag NPs on the outer surface of mordenite is explained by the redox interaction of Ag⁺-Fe²⁺ and the selectivity of ion exchange. The local surrounding of Ag in the studied samples is different: for AgMOR—monatomic species dominate, FeAgMOR—silver dimers and AgFeMOR—metal particles. In all investigated samples, the partially charged intra-channel Ag_n^δ+ clusters (~0.7 nm in size) were formed due to partial Ag⁺ reduction and subsequent Ag⁰ agglomeration into the mordenite channel. Most of the silver in the bulk of the zeolite is represented in the cationic state attached to the mordenite framework by differently coordinated electrostatic forces, which can be Ag-O, Ag-Si or Ag-Al, with variations in interatomic distances and do not depend on the order of metal deposition. In addition, the arrangement of the cations in the side pockets means that the transport channels of mordenite are free, which is favorable for the application of the materials under study in catalysis and adsorption. Full article

Faujasite zeolites with a regular micropore and mesopore structure have been considered desirable scaffolds to stabilize luminescent silver nanoclusters (Ag CLs), while turning of the emission properties of the confined Ag CLs is still under investigation. In this study, the desilicated and dealuminated faujasite zeolites were first prepared to modify the zeolite framework and Si/Al ratio before Ag⁺ loading. With thermal treatment on the thereafter Ag⁺-exchanged zeolites, the Ag CLs formatted inside the D6r cages showed red-shifted emission in the desilicated zeolites and blue-shifted emission in the dealuminated zeolites, so that a tunable emission in the wavelength range of 482–528 nm could be obtained. Meanwhile, the full width at half maximum of the emission spectra is also closely related with framework modification, which monotonously increases with enhancing Si/Al ratio of host zeolite. The XRD, XPS, and spectral measurements indicated that the tunable luminescence properties of Ag CLs result from the controlling of local crystal field and coupling between host lattice and luminescent center. This paper proposes an effective strategy to manipulate the emission properties of Ag CLs confined inside zeolites and may benefit the applications of noble metal clusters activated phosphors in imaging and tunable emission. Full article