Search Results (48)

Chemical warfare agents (CWAs) pose severe threats to human health and the environment because of their extreme toxicity. Conventional liquid-phase decontamination processes can present limitations, including potential equipment corrosion, generation of secondary liquid waste, and increased operational complexity. To overcome these challenges, we report a solar-assisted process intensification strategy for solvent-free decontamination of toxic organophosphorus compounds using UiO-66-NH₂@carbon nanotube (CNT) hybrid platforms. Incorporation of CNTs (optimized at 5 wt%) enables efficient solar-to-thermal conversion, resulting in rapid photothermal self-heating to 85 °C under simulated solar irradiation (1000 W m⁻²). This localized thermal effect contributes to accelerated DMMP removal within the MOF-based hybrid structure, thereby partially alleviating the kinetic limitations typically associated with solvent-free reactions. Consequently, the optimized hybrid achieves 94% removal of dimethyl methylphosphonate (DMMP), a representative sarin simulant, within 10 min under humidity-conditioned, solvent-free conditions, representing a 27% improvement compared with pristine UiO-66-NH₂. This decontamination platform eliminates the need for chemical solvents and external energy input, thereby mitigating secondary contamination and reducing the environmental footprint. By integrating the catalytic framework of Zr-based MOFs with the photothermal capability of CNTs, this study presents a sustainable engineering strategy for advanced defense and environmental protection. Full article

Dry reforming of methane (DRM) converts the greenhouse gases methane (CH₄) and carbon dioxide (CO₂) into syngas (hydrogen (H₂) and carbon monoxide (CO)). Despite its numerous advantages, DRM has not yet been industrialized due to catalyst deactivation and competing side reactions. While Ni-based catalysts have been widely used, they are prone to increased carbon deposition and sintering, and although bimetallic systems and oxygen-based supports have shown promise, their effects on carbon deposition are yet to be fully understood. In this study, carbon nanotube (CNT)-supported Pt-Ni catalysts incorporating mixed oxides of CeZrO₂ and CeZrLaO₂ were investigated to evaluate the impact of support composition and metal–support interactions in DRM. The catalysts were synthesized and subsequently tested in DRM. Catalysts supported on CNTs displayed higher CH₄ and CO₂ conversions compared to conventional ceria–zirconia, highlighting the beneficial role of the carbon nanotube support in improving dispersion and accessibility of the metal active sites. Addition of Pt was found to promote reverse water–gas shift (RWGS) reaction, whereas the addition of La was found to decrease catalytic activity. Despite the formation of a Ni-Pt alloy, the obtained catalysts favored RWGS over DRM. These findings illustrate key limitations and design considerations for optimization of CNT-supported bimetallic catalysts in DRM. Full article

Metal oxide nanomaterials have emerged as transformative materials in the quest to enhance the energy density and overall performance of lithium-ion batteries (LIBs) and solid-state batteries (SSBs). Their unique properties—including their large surface areas and short ion diffusion pathways—make them ideal for next-generation energy storage technologies. In LIBs, the high surface-to-volume ratio of metal oxide nanomaterials significantly enlarges the active interfacial area and shortens the lithium-ion diffusion paths, leading to an improved high-rate performance and enhanced energy density. Transition metal oxides (TMOs) such as nickel oxide (NiO), copper oxide (CuO), and zinc oxide (ZnO) have demonstrated significant theoretical capacities, while binary systems like NiCuO offer further improvements in cycling stability and energy output. Additionally, layered lithium-based TMOs, particularly those incorporating nickel, cobalt, and manganese, have shown remarkable promise in achieving high specific capacities and long-term stability. The synergistic integration of metal oxides with carbon-based nanostructures, such as carbon nanotubes (CNTs), enhances the electrical conductivity and structural durability further, leading to a superior electrochemical performance in LIBs. In SSBs, the use of oxide-based solid electrolytes like garnet-type Li₇La₃Zr₂O₁₂ (LLZO) and sulfide-based electrolytes has facilitated the development of high-energy-density systems with excellent ionic conductivity and chemical stability. However, challenges such as high interfacial resistance at the electrode–electrolyte interface persist. Strategies like the application of lithium niobate (LiNbO₃) coatings have been employed to enhance interfacial stability and maintain electrochemical integrity. Furthermore, two-dimensional (2D) metal oxide nanomaterials, owing to their high active surface areas and rapid ion transport, have demonstrated considerable potential to boost the performance of SSBs. Despite these advancements, several challenges remain. Morphological optimization of nanomaterials, improved interface engineering to reduce the interfacial resistance, and solutions to address dendrite formation and mechanical degradation are critical to achieving the full potential of these materials. Full article

This study compares unsupported NiO nanoflowers (NiEG) and ZrO₂-supported NiO (25NiZ) for methane activation and hydrogenation, focusing on the impact of catalyst morphology. The NiEG catalyst demonstrated superior performance, achieving a high methane activation rate of 1.79 mol/(s·g_NiO) and unique product selectivity. It produced ethylene and ethane at 503 K and higher hydrocarbons (C₄–C₆) at 593 K. Furthermore, the NiEG catalyst exhibited enhanced coke resistance, forming less-deactivating carbon nanotubes compared to the filamentous coke prevalent on the 25NiZ catalyst. We attribute this performance to the nanoflower morphology, which provides highly exposed and stable Ni sites that facilitate C-H cleavage and stabilize reaction intermediates. Full article

Carbon nanotube field-effect transistors (CNT FETs) are considered strong candidates for next-generation flexible electronics due to their excellent carrier mobility and mechanical flexibility. However, the fabrication of CNT FETs on conventional flexible substrates such as PI or PET is often limited by surface roughness, chemical incompatibility, and poor mechanical robustness, resulting in degraded device performance. In this study, we report the fabrication of buried-gate CNT FETs incorporating Hf_0.5Zr_0.5O₂ as the gate dielectric on mica substrates, which offer high surface flatness, low defect density, and superior mechanical durability. The fabricated devices exhibit outstanding electrical characteristics, including a field-effect mobility of 38.4 cm²/V·s, a subthreshold swing of 93 mV/dec, and a transconductance of 14.2 μS. These results demonstrate the excellent mechanical stability and reliable electrical performance of the proposed devices under bending stress, highlighting their suitability for mechanically demanding flexible electronics applications. Full article

The production of synthetic natural gas in the context of power-to-gas is a promising technology for the utilization of CO₂. Ni-based catalysts supported on carbon nanotubes (CNTs) were prepared through incipient wetness impregnation and characterized using N₂ adsorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and temperature-programmed reduction (TPR). The catalysts were tested for CO₂ methanation in the 200–400 °C temperature range and at atmospheric pressure. The results demonstrated that the catalytic activity increased with the addition of the CNTs and Ni loading. The selectivity towards CH₄ was close to 100% for the Ni/ZrO₂/CNT catalysts. Reduction of the calcined catalyst at 500 °C using H₂ modified the surface chemistry of the catalyst, leading to an increase in the Ni particles. The CO₂ conversion was dependent on the Ni loading and the temperature reduction in the NiO species. The 10Ni/ZrO₂/CNT catalyst was highly stable in CO₂ methanation at 350 °C for 24 h. Thus, CNTs combined with Ni and ZrO₂ were considered promising for use as catalysts in CO₂ methanation at low temperatures. Full article

Nanostructures obtained as a by-product of the electrochemical synthesis of ZrO₂ nanotube membranes have scarcely received any attention despite their enormous potential. This is mainly due to their size properties, morphology, and composition. In the present work, these nanostructures are characterized, and their potential application as an additive in PVA-based coatings is analyzed. The characterization was performed by X-ray fluorescence, scanning electron microscopy, energy-dispersive X-ray spectroscopy, transmission electron microscopy, and X-ray diffraction. The results showed that the nanostructures consist of tubular fragments generated during the formation of the ZrO₂ membrane, with a dimension of 626.74 nm in width, a length of 1906.39 nm, and a clear cubic structure. The ZrO₂-PVA coating, which is prepared by using the spin coating technique, presented a uniform and homogenous particle distribution, which was later confirmed by Fourier transform infrared spectroscopy, scanning electron microscopy, and atomic force microscopy. The optical transparency and thermal resistance were evaluated through UV-Vis spectroscopy and thermogravimetric analysis, showing that the incorporation of ZrO₂ as an additive improved its UV absorption properties and thermal stability during the pyrolysis stage. The results suggest that the ZrO₂ nanostructures enhance the thermal and protective properties of the PVA-based coatings by acting as physical barriers and stabilizers within the polymer matrix. Full article

ZrO₂ and multi-walled carbon nanotubes (MWCNTs) were selected as single-phase and composite toughening agents to investigate the influence on the mechanical properties of CaZr₄(PO₄)₆ (CZP) ceramics. The results revealed that the addition of single-phase or composite toughening agents had minimal impact on the phase composition and crystallinity of CZP ceramics. When the content of the single-phase ZrO₂ toughening agent reached 10 wt.%, the flexural strength of CZP ceramics increased to 71.60 MPa due to the particle toughening mechanism of ZrO₂. With the addition of 1.0 wt.% ZrO₂ and 0.3 wt.% MWCNTs, the CZP ceramics demonstrated enhanced densification and improved sintering activity. The small-sized ZrO₂ particles were evenly dispersed within the ceramic matrix, accompanied by a phase transformation during sintering. Together with MWCNTs, this combination resulted in a significant increase in flexural strength, reaching 138.43 MPa. An in-depth analysis of the toughening mechanisms indicated that the CZP ceramic matrix primarily featured ZrO₂ phase transformation toughening and the pull-out and bridging toughening provided by MWCNTs. The synergistic interaction of these multiple toughening mechanisms significantly enhanced the mechanical properties of CZP ceramics, providing valuable theoretical insights for optimizing the performance of phosphate ceramics in practical applications. Full article

In this study, a Brönsted–Lewis bifunctional acidic catalyst PW/UiO/CNTs-OH was synthesized via the hydrothermal method. The parameters for the esterification reaction of oleic acid with methanol catalyzed by PW/UiO/CNTs-OH were optimized using central composite design-response surface methodology (CCD-RSM). A biodiesel yield of 92.9% was achieved under the optimized conditions, retaining 82.3% biodiesel yield after four catalytic cycles. The enhanced catalytic performance of PW/UiO/CNTs-OH can be attributed as follows: the [Zr₆O₄(OH)₄]¹²⁺ anchored on the surface of multi-walled carbon nanotubes (MWCNTs) can serve as nucleation sites for UiO-66, not only encapsulating H₃[P(W₃O₁₀)₄] (HPW) but also reversing the quadrupole moment of MWCNTs to generate Lewis acid sites. In addition, introduction of HPW during synthesis of UiO-66 decreases the solution pH, inducing the protonation of p-phthalic acid (PTA) to disrupt the coordination with the [Zr₆O₄(OH)₄] cluster, thereby creating an unsaturated Zr⁴⁺ site with electron pair-accepting capability, which generates Lewis acid sites. EIS analysis revealed that PW/UiO/CNTs-OH has higher electron migration efficiency than UiO-66 and PW/UiO. Furthermore, NH₃-TPD and Py-IR analyses showed that PW/UiO/CNTs-OH possessed high densities of Lewis acidic sites of 83.69 μmol/g and Brönsted acidic sites of 9.98 μmol/g. Full article

Nanotechnology can improve crop yield and quality by improving seed germination and growth conditions. We chose multi walled carbon nanotubes (MWCNTs) and nano silica (nano-SiO₂) for exploring the effects of different concentrations of MWCNTs and nano-SiO₂ on key enzymes for germination and endogenous hormone level in maize. The results indicate that MWCNTs and nano-SiO₂ can promote seed germination characteristics, such as the germination potential, germination rate, germination index, storage material transport rate, radicle and germ biomass of maize seeds. Amounts of 800 mg·L⁻¹ MWCNTs and 1500 mg·L⁻¹ nano-SiO₂ showed a positive effect on germination index, and nano-SiO₂ was better than MWCNTs in promoting germination effects. Most importantly, MWCNTs and nano-SiO₂ can improve the activities of amylase in maize grain, cytochrome oxidase (COX) and alternating oxidase (AOX) in seed embryo and key enzymes of glycolysis, so as to accelerate the hydrolysis of carbohydrates such as starch, provide energy and material basis for seed germination, improve seed vitality and promote seed germination. MWCNTs and nano-SiO₂ can enhance the content of key hormones in promoting roots and leaves, including decreased content of abscisic acid (ABA) and increased contents of methyl jasmonate (MeJA), auxin (IAA), gibberellin (GA), and zeaxanthin (ZR), which result directly in achieving an available balance of MeJA/ABA, GA/ABA, ZR/ABA, and IAA/ABA ratios between different hormone contents, providing support for the growth development of maize kernels and seedlings. Full article

Engineering ceramics and their composites are widely used owing to their excellent properties, including high wear, corrosion and heat resistance, low friction coefficient, and low thermal conductivity; thus, the current paper presents a comprehensive review of the most common types of engineering ceramics, demonstrating their key properties, advantages, potential applications, and challenges. This paper also provides prevailing methods for tackling the engineering ceramic challenges and maximizing their applicability. This review paper focuses on alumina (Al₂O₃), silicon carbide (SiC), zirconia (ZrO₂), aluminum nitride (AlN), and silicon nitride (Si₃N₄), and explores their usability in automotive, aerospace, and tribological applications. Additionally, the incorporation of reinforcing nanomaterials, i.e., graphene and carbon nanotubes or their combination with second-phase reinforcing nanomaterials in these types of ceramics to improve their physico-mechanical properties is also discussed. By strategically adding these reinforcing materials, the brittleness of ceramics can be mitigated, leading to materials that are more suitable for demanding applications in various high-performance industries. Full article

Double-walled carbon nanotube-yttria-stabilized ZrO₂ nanocomposites are prepared by a mixing route followed by Spark Plasma Sintering. The double-walled carbon nanotubes (DWCNTs) have been previously subjected to a covalent functionalization. The nanocomposites present a high densification and show a homogenous dispersion of DWCNTs into a matrix about 100 nm in size. The DWCNTs are well distributed at the matrix grain boundaries but form larger bundles upon the increase in carbon content. The Vickers microhardness of the nanocomposites decreases regularly upon the increase in carbon content. Incorporation of carbon at contents higher than 2 wt.% results in significantly lower friction coefficients, both against alumina and steel balls, possibly because of the elastic deformation of the DWCNTs at the surface of the sample. Their presence also favors a reduction of the steel/ceramic contacts and reduces the wear of the steel ball at high loads. DWCNTs improve wear resistance and reduce friction without incurring any severe damage, contrary to multi-walled carbon nanotubes. Full article

Additive manufacturing technologies can be used to fabricate 3D-printed dental restorations. In this study, we evaluated the effectiveness of the functionalized loading of zirconium dioxide (ZrO₂) nanoparticles and silver-nanoparticles-immobilized halloysite (HNC/Ag) nanotubes into 3D printing resins. We created 3D printing resins by adding different mass fractions of ZrO₂ and HNC/Ag. First, six groups of samples containing ZrO₂ were prepared, comprising five groups with different mass fractions and one control group of ZrO₂ containing 1 to 16 %wt. Different mass fractions of HNC/Ag fillers were combined with the ZrO₂ mixture and resin at the ideal ratio from 1 to 7.5 %wt. The mechanical characteristics of 3D resin that we assessed were the flexural strength, flexural modulus, fracture toughness, and the microhardness. Additional rates of ZrO₂ 4 %wt. and HNC/Ag 5 %wt. significantly increase the flexural strength, flexural modulus, and fracture toughness compared to the control group (p < 0.001). ZrO₂ 16 %wt. and HNC/Ag 5 %wt. were found to be significantly harder compared to the other groups (p < 0.001). The amounts of NPs that can be added to 3D printing resin modification appears to be 4 %wt., and HNC/Ag 5 %wt. can be advantageous in terms of fracture toughness, flexural strength, and flexural modulus. All additions of nanoparticles raised the resin’s hardness. Full article

This work examines the cooperative effect between Zr doping and oxygen vacancy engineering in anodized TiO₂ nanotubes (TNTs) for enhanced oxygen reduction reactions (ORRs). Zr dopant and annealing conditions significantly affected the electrocatalytic characteristics of grown TNTs. Zr doping results in Zr⁴⁺ substituted for Ti⁴⁺ species, which indirectly creates oxygen vacancy donors that enhance charge transfer kinetics and reduce carrier recombination in TNT bulk. Moreover, oxygen vacancies promote the creation of unsaturated Ti³⁺(Zr³⁺) sites at the surface, which also boosts the ORR interfacial process. Annealing at reductive atmospheres (e.g., H₂, vacuum) resulted in a larger increase in oxygen vacancies, which greatly enhanced the ORR activity. In comparison to bare TNTs, Zr doping and vacuum treatment (Zr:TNT–Vac) significantly improved the conductivity and activity of ORRs in alkaline media. The finding also provides selective hydrogen peroxide production by the electrochemical reduction of oxygen. Full article

Titanium-zirconium dioxide nanostructures loaded by hydroxyapatite were produced on the surface of Ti65Zr alloy. The alloy was treated by anodization with the subsequent immersion in calcium glycerophosphate (CG) solutions. The resulting surfaces present TiO₂-ZrO₂ nanotubular (TiZr-NT) structures enriched with hydroxyapatite (HAP). The nanotube texture is expected to enhance the surface’s corrosion resistance and promote integration with bone tissue in dental implants. The TiZr-NT structure had a diameter of 73 ± 2.2 nm and a length of 10.1 ± 0.5 μm. The most favorable result for the growth of HAP in Hanks’ balanced salt solution (Hanks’ BSS) was obtained at a CG concentration of 0.5 g/L. Samples soaked in CG at a concentration of 0.5 g/L demonstrated in a decrease of the contact angles to 25.2°; after 3 days of exposure to Hanks’ BSS, the contact angles further reduced to 18.5°. The corrosion studies also showed that the TiZr-NT structure soaked in the CG = 0.5 g/L solution exhibited the best corrosion stability. Full article