Search Results (64)

Plastic waste and water pollution demand circular economy-driven innovations. This review examines metal–organic framework (MOF) synthesis from polyethylene terephthalate (PET) waste for wastewater treatment. Depolymerized PET yields terephthalic acid and ethylene glycol—essential MOF precursors. We evaluate the following: (1) PET depolymerization (hydrolysis, glycolysis, ammonolysis) for monomer recovery efficiency; (2) MOF synthesis (solvothermal, microwave, mechanochemical) using PET-derived linkers; (3) performance in adsorbing heavy metals, dyes, and emerging contaminants. PET-based MOFs match or exceed commercial adsorbents in pollutant removal while lowering costs. Their tunable porosity and surface chemistry enhance selectivity and capacity. By converting waste plastics into functional materials, this strategy tackles dual challenges: diverting PET from landfills and purifying water. The review underscores the environmental and economic benefits of waste-sourced MOFs, proposing scalable routes for sustainable water remediation aligned with zero-waste goals. Full article

Covalent organic framework (COF) membranes have garnered significant attention in ion separation due to their high surface area, tunable pore size, excellent stability, and diverse functional groups. Over the past decade, various synthesis methods, such as solvothermal synthesis, interfacial synthesis, microwave-assisted solvothermal synthesis, and in situ growth, have been developed to fabricate COF membranes. COF membranes have demonstrated remarkable ion separation performance in different separation processes driven by pressure, electric field, and vapor pressure difference, showing great potential in a wide range of applications. Nevertheless, challenges in the synthesis and application of COF membranes still remain, requiring further research to fully realize their potential in ion separation. This review critically examines the development of COF membranes, from synthesis methods to ion separation applications. We evaluate the advantages and limitations of various synthesis techniques and systematically summarize COF membrane performance based on separation driving forces. Finally, we present a critical analysis of current challenges and offer perspectives on promising future research directions for advancing COF membrane technology in separation. Full article

Metal–organic frameworks (MOFs), particularly zirconium-based frameworks (Zr-MOFs), have gained significant attention in recent years due to their unique structural and functional properties. This review focuses on eco-friendly synthetic methods for producing Zr-MOFs, addressing the environmental impacts and costs associated with conventional synthesis, which often relies on hazardous reagents and harsh conditions. We explore various green synthesis strategies, including the selection of raw materials (such as using zirconium acetate), organic ligands (recycling waste materials for ligand synthesis), and synthesis methods (solvothermal, microwave-assisted, ultrasound-assisted, electrochemical, and mechanochemical approaches). Additionally, the application of Zr-MOFs in photocatalysis and electrocatalysis is examined, highlighting their potential for environmental purification and energy conversion. Despite the progress made in laboratory settings, challenges remain in achieving cost-effectiveness, material stability, and scalability for industrial applications. Future research should concentrate on enhancing synthesis efficiency, optimizing catalytic properties, investigating structure–property relationships, and expanding applications to novel catalytic reactions, thus ensuring Zr-MOFs can contribute to sustainable development in chemical science and technology. Full article

Cesium tungsten bronzes (Cs_xWO₃), as functional materials with excellent near-infrared shielding properties, demonstrate significant potential for applications in smart windows. However, traditional synthesis methods, such as solid-state reactions and solvothermal/hydrothermal approaches, typically require harsh conditions, including high temperatures (above 200 °C), high pressure, inert atmospheres, or prolonged reaction times. In this study, we propose an optimized microwave-assisted solvothermal synthesis strategy that significantly reduces the severity of reaction conditions through precise parameter control. When benzyl alcohol was employed as the solvent, Cs_xWO₃ nanoparticles could be rapidly synthesized within a relatively short duration of 15 min at 180 °C, or alternatively obtained through 2 h at a low temperature of 140 °C. However, when anhydrous ethanol, which is cost-effective and environmentally friendly, was substituted for benzyl alcohol, successful synthesis was also achieved at 140 °C in 2 h. This method overcomes the limitations of traditional high-pressure reaction systems, achieving efficient crystallization under low-temperature and ambient-pressure conditions while eliminating safety hazards and significantly improving energy efficiency. The resulting materials retain excellent near-infrared shielding performance and visible-light transparency, providing an innovative solution for the safe, rapid, and controllable synthesis of functional nanomaterials. Full article

3d transition metal oxides composed of Mn, Fe, Co, and Ni have emerged as promising candidates for supercapacitor electrode materials due to their high theoretical specific capacitance, abundant redox-active sites, variable oxidation states, environmental friendliness, and low cost. Various synthesis strategies have been developed to fabricate these nanostructures, including hydrothermal/solvothermal methods, sol–gel processing, and microwave-assisted synthesis. Among them, microwave irradiation technology, with its rapid heating characteristics and unique thermal/non-thermal effects, offers significant advantages in controlling crystallinity and particle size distribution, suppressing particle agglomeration, and enhancing material purity. Furthermore, microwave effects facilitate the self-assembly and morphological evolution of transition metal oxides, promote the formation of crystal defects, and strengthen interfacial interactions. These effects enable precise microstructural tuning, leading to an increased specific surface area and a higher density of active sites, ultimately enhancing specific capacitance, rate capability, and cycling stability. In recent years, microwave-assisted synthesis has made significant progress in constructing 3d transition metal oxides and their composites, particularly in the development of single-metal and binary-metal oxides, as well as their hybrids with carbon-based materials (e.g., graphene and carbon nanotubes) and other metal oxides. This review systematically summarizes the research progress on microwave-assisted techniques for 3d transition metal oxide-based nanomaterials, with a particular focus on the role of microwave effects in morphology control, interfacial optimization, and electrochemical performance enhancement. Additionally, key challenges in current research are critically analyzed, and potential optimization strategies are proposed. This review aims to provide new insights and perspectives for advancing microwave-assisted synthesis of 3d transition metal oxides in energy storage applications. Full article

Metal–organic frameworks (MOFs) have garnered significant attention for water purification in recent years. In particular, UiO-66 (a member of the UiO-MOF family, developed at the University of Oslo) has emerged as a promising water purification material. UiO-66 exhibits excellent adsorption through electrostatic interaction, π–π stacking and Lewis acid–base coordination mechanisms. The photocatalytic degradation property was enhanced through metal doping, composite with semiconductor materials, defect engineering, etc., and the removal efficiency of pollutants was significantly improved. This review systematically describes the structure of UiO-66 and the synthesis methods of UiO-66, including solvothermal, microwave-assisted, mechanized and electrochemical methods, as well as the application of UiO-66 in the adsorption and photocatalytic degradation of various pollutants. Full article

CDs/TiO₂ nanohybrids were synthesized and tested for photocatalytic H₂ production from aqueous media through simulated solar light-driven photocatalytic reactions. Firstly, three different types of CDs were prepared through green methods, specifically hydrothermal treatment and microwave irradiation, using citric acid and urea as precursors in varying molar ratios. After a multi-step purification procedure, impurity-free CDs were obtained. The as-synthesized CDs were thoroughly characterized using UV-Vis, FT-IR, and PL spectroscopy, along with HR-TEM. The results revealed that the size and optical and physicochemical properties of CDs can be tailored by selecting the precursors’ ratio and the synthetic approach. The heterostructured CDs/TiO₂ photocatalysts were formed solvothermally and were analyzed using UV-Vis/DRS, FT-IR, and XPS techniques, which confirmed the effective incorporation of CDs and the improved properties of TiO₂. The use of sacrificial reagents is among the most common strategies for enhancing H₂ production from water through photocatalytic processes; herein, ethanol was selected as a green liquid organic hydrogen carrier. A maximum H₂ production rate of 0.906 μmol H₂/min was achieved, while the recyclability study demonstrated that the photocatalyst maintained stable performance during multiple cycles of reuse. Thus, optimizing the synthesis conditions of CDs/TiO₂ nanohybrids resulted in the creation of environmentally friendly and reusable photocatalysts. Full article

Carbon dots (CDs), a versatile class of fluorescent carbon-based nanomaterials, have attracted widespread attention due to their exceptional optical properties, biocompatibility, and cost-effectiveness. Their applications span biomedicine, optoelectronics, and smart food packaging, yet large-scale synthesis remains a significant challenge. This review categorizes large-scale synthesis methods into liquid-phase (hydrothermal/solvothermal, microwave-assisted, magnetic hyperthermia, aldol condensation polymerization), gas-phase (plasma synthesis), solid-phase (pyrolysis, oxidation/carbonization, ball milling), and emerging techniques (microfluidic, ultrasonic, molten-salt). Notably, microwave-assisted and solid-state synthesis methods show promise for industrial production due to their scalability and efficiency. Despite these advances, challenges persist in optimizing synthesis reproducibility, reducing energy consumption, and developing purification methods and quality control strategies. Addressing these issues will be critical for transitioning CDs from laboratory research to real-world applications. Full article

Incorporating nanoparticles into denture materials shows promise for the prevention of denture-associated fungal infections. This study investigates the antifungal properties of acrylic modified with microwave-sintered ZnO-Ag nanoparticles. ZnO-Ag nanoparticles (1% and 2.5% wt.) were synthesized via microwave solvothermal synthesis (MSS). Nanoparticles were characterized for phase purity, specific surface area (SSA), density, morphology, and elemental composition. ZnO and ZnO-Ag nanoparticles were added to acrylic material (PMMA) at concentrations of 1% and 2.5% and polymerized. Pure PMMA (control) and obtained PMMA-nanocomposites were cut into homogeneous 10 × 10 mm samples. Antifungal activity of nanoparticles and PMMA-nanocomposites against C. albicans was tested using minimal inhibitory concentration (MIC) determination, and biofilm formation was assessed using crystal violet staining followed by absorbance measurements. Laboratory tests confirmed phase purity and uniform, spherical particle distribution. MIC results show antifungal activity of 1% Ag nanoparticles and the PMMA-2.5% (ZnO-1% Ag) nanocomposite. PMMA-1% (ZnO-1% Ag) nanocomposite and 1% ZnO-Ag nanoparticles are efficient in preventing biofilm formation. However, ZnO nanoparticles showed antibiofilm activity, and the PMMA-ZnO nanocomposite does not protect against biofilm deposition. Incorporating hybrid ZnO-Ag nanoparticles into PMMA is a promising antibiofilm method, especially with ZnO-1% Ag nanoparticles. Full article

In recent decades, nanoscience has experienced rapid global advancements due to its focus on materials and compounds at the nanoscale with high efficiency across diverse applications. WO₃ nanostructures have proven to be a unique material in the development of new technologies due to their electrical, optical, and catalytic properties. They have been used as raw materials for the fabrication of electrochromic devices, optoelectronic devices, hydrogenation catalysts, gas sensors, adsorbents, lithium-ion batteries, solar driven-catalysts, and phototherapy. One of the most striking characteristics of WO₃ is its morphological diversity, spanning from 0D to 2D, encompassing nanoparticles, nanowires, nanofibers, nanorods, nanosheets, and nanoplates. This review discusses common synthesis methods for WO₃ nanostructures, including hydrothermal and solvothermal methods, microwave-assisted synthesis, sol-gel, electrospinning, co-precipitation, and solution combustion, with emphasis on the advantages and challenges of each of them. The processes involved, the obtained morphologies, and the resulting applications are also presented. As evidenced here, the fine control of the synthesis parameters allows the production of nanostructures with controlled phase, morphology, and size, essential aspects for the production of high-performance WO₃-based devices. Full article

Sweat is considered the most promising candidate to replace conventional blood samples for noninvasive sensing. There are many tools and optical and electrochemical methods that can be used for detecting sweat biomarkers. Electrochemical methods are known for their simplicity and cost-effectiveness. However, they need to be optimized in terms of selectivity and catalytic activity. Therefore, electrode modifiers such as nanostructures and metal–organic frameworks (MOFs) or combinations of them were examined for boosting the performance of the electrochemical sensors. The MOF structures can be prepared by hydrothermal/solvothermal, sonochemical, microwave synthesis, mechanochemical, and electrochemical methods. Additionally, MOF nanostructures can be prepared by controlling the synthesis conditions or mixing bulk MOFs with nanoparticles (NPs). In this review, we spotlight the previously examined MOF-based nanostructures as well as promising ones for the electrochemical determination of sweat biomarkers. The presence of NPs strongly improves the electrical conductivity of MOF structures, which are known for their poor conductivity. Specifically, Cu-MOF and Co-MOF nanostructures were used for detecting sweat biomarkers with the lowest detection limits. Different electrochemical methods, such as amperometric, voltammetric, and photoelectrochemical, were used for monitoring the signal of sweat biomarkers. Overall, these materials are brilliant electrode modifiers for the determination of sweat biomarkers. Full article

The adsorption properties of microporous carbon materials modified with iron citrate were investigated. The carbon materials were produced based on resorcinol-formaldehyde resin, treated in a microwave assisted solvothermal reactor, and next carbonized in the tube furnace at a temperature of 700 °C under argon atmosphere. Iron citrate was applied as a modifier, added to the material precursor before the synthesis in the reactor, in the quantity enabling to obtain the nanocomposites with C:Fe mass ratio equal to 10:1. Some samples were additionally activated using potassium oxalate or potassium hydroxide. The phase composition of the produced nanocomposites was determined using the X-ray diffraction method. Scanning and transmission electron microscopy was applied to characterize the changes in samples’ morphology resulting from the activation process and/or the introduction of iron into the carbon matrix. The adsorption of nitrogen from gas phase and dyes (methylene blue and congo red) from water solution on the obtained materials was investigated. In the case of methylene blue, the adsorption equilibrium isotherms followed the Langmuir isotherm model. However, in the case of congo red, a linear dependency of adsorption and concentration in a broad equilibrium concentration range was found and well-described using the Henry equation. The most efficient adsorption of methylene blue was noticed for the sample activated with potassium hydroxide and modified with iron citrate, and a maximum adsorption capacity of 696 mg/g was achieved. The highest congo red adsorption was noticed for the non-activated sample modified with iron citrate, and the partition coefficient for this material equaled 171 dm³/g. Full article

Zeolitic imidazolate frameworks (ZIFs) are traditionally synthesized using N, N-dimethylformamide (DMF). However, DMF is toxic and hazardous to human health and the environment, hence other alternative solvents need to be considered. Herein, three different solvents like methanol, water and acetone were used to replace DMF and to explore the syntheses of ZIF-90 using a conventional and a microwave-assisted solvothermal method to obtain hydrothermally stable products, which also exhibit an increased water uptake. Pure ZIF-90 was synthesized under ambient pressure at 60 °C for 90 min using the conventional solvothermal method in an acetone–water solution, while under microwave irradiation it was formed in only 5 min at 80 °C. Altering methanol, water and acetone in the reaction mixture significantly affected the structural and water adsorption properties of ZIF-90s, which were monitored via PXRD, TGA, nitrogen and water sorption, and SEM. The highly efficient, less toxic, low-cost and activation-free microwave synthesis resulted in the formation of ZIF-90 nanoparticles that exhibited the highest maximum water adsorption capacity (0.37 g/g) and the best hydrothermal stability between water adsorption at 30 °C and desorption at 100 °C at 12.5 mbar among all the products obtained. Full article

Rare earth bisphthalocyanines (MPc₂) are of particular interest because of their behavior as single-molecular magnets, which makes them suitable for applications in molecular spintronics, high-density data storage and quantum computation. Nevertheless, MPc₂ are not commercially available, and the synthesis routes are mainly focused on obtaining substituted phthalocyanines. Two preparation routes depend on the precursor: synthesis from phthalonitrile (PN) and the metalation of free or dilithium phthalocyanine (H₂Pc and Li₂Pc). In both options, byproducts such as free-base phthalocyanine and in the first route additional PN oligomers are generated, which influence the MPc₂ yield. There are three preparation methods for these routes: heating, microwave radiation and reflux. In this research, solvothermal synthesis was applied as a new approach to prepare yttrium, lanthanum, gadolinium and terbium unsubstituted bisphthalocyanines using Li₂Pc and the rare earth(III) acetylacetonates. Purification by sublimation gave high product yields compared to those reported, namely 68% for YPc₂, 43% for LaPc₂, 63% for GdPc₂ and 62% for TbPc₂, without any detectable presence of H₂Pc. Characterization by infrared, Raman, ultraviolet–visible and X-ray photoelectron spectroscopy as well as elemental analysis revealed the main featuresof the four bisphthalocyanines, indicating the success of the synthesis of the complexes. Full article

Nitrogen dioxide (NO₂) gas sensors are pivotal in upholding environmental integrity and human health, necessitating heightened sensitivity and exceptional selectivity. Despite the prevalent use of metal oxide semiconductors (MOSs) for NO₂ detection, extant solutions exhibit shortcomings in meeting practical application criteria, specifically in response, selectivity, and operational temperatures. Here, we successfully employed a facile microwave-solvothermal method to synthesize a mesoporous CeO₂/CNCs nanocomposite. This methodology entails the rapid and comprehensive dispersion of CeO₂ nanoparticles onto helical carbon nanocoils (CNCs), resulting in augmented electronic conductivity and an abundance of active sites within the composite. Consequently, the gas-sensing sensitivity of the nanocomposite at room temperature experienced a notable enhancement. Moreover, the presence of cerium oxide and the conversion of Ce³⁺ and Ce⁴⁺ ions facilitated the generation of oxygen vacancies in the composites, thereby further amplifying the sensing performance. Experimental outcomes demonstrate that the nanocomposite exhibited an approximate 9-fold increase in response to 50 ppm NO₂ in comparison to pure CNCs at room temperature. Additionally, the CeO₂/CNCs sensor displayed remarkable selectivity towards NO₂ when exposed to gases such as NH₃, CO, SO₂, CO₂, and C₂H₅OH. This straightforward microwave-solvothermal method presents an appealing strategy for the research and development of intelligent sensors based on CNCs nanomaterials. Full article