Search Results (516)

Introduction: Chronic kidney disease (CKD) increases cardiovascular risk through mechanisms such as oxidative stress and the accumulation of advanced glycation end products (AGEs). Glycated albumin (GA) is associated with cardiovascular risk in CKD patients, but its relationship with AGEs and systemic inflammation remains unclear. This study investigated these associations in old patients with severe CKD, with and without diabetes. Methods: We conducted a cross-sectional analysis in 122 patients aged ≥ 65 years with CKD stages G3a–G5, including 67 diabetics and 55 non-diabetics. Patients with confounding comorbidities were excluded. We measured GA, AGEs, various AGEs receptors (RAGE) isoforms, and inflammatory cytokines (CRP, IL-6, TNFα, and MCP-1) using standardized assays. Statistical analyses included group comparisons, correlation coefficients, and multivariate regression. Results: Of 122 patients (mean age 77.7 ± 11.3 years), diabetics had higher GA percentages than non-diabetics (22.0 ± 7.1% vs. 17.5 ± 5.4%, p = 0.0001), while AGEs (2931 ± 763 vs. 3156 ± 809 AU; p = 0.118) and inflammatory markers (CRP 0.240[0.380] vs. 0.200[0.280] mg/dL; p = 0.142; IL-6 3.4[4.0] vs. 3.0[3.8] pg/mL; p = 0.238) were similar between groups. Overall, GA was inversely correlated with estimated glomerular filtration rate (eGFR) (ρ = −0.189, p = 0.037) and positively with glycated hemoglobin (HbA1c) (ρ = 0.525, p < 0.0001), but showed no significant correlation with AGEs, RAGE isoforms, or inflammatory cytokines. In multivariate analysis, only HbA1c remained independently associated with GA (β = 0.222, p = 0.005). Conclusions: In old patients with severe CKD, GA appears to be a more useful marker of glycemic control than glycation stress, the latter of which is the result of multiple factors, including impaired kidney function and systemic inflammation. Full article

In the absence of appropriate tools and a knowledge base for exploring high-grade metamorphic terrains, felsic gneiss complexes at granulite facies have long been considered barren and have remained undermapped and understudied. This was the case of the Bondy gneiss complex in the southwestern Grenville Province of Canada which consists of 1.39–1.35 Ga volcanic and plutonic rocks metamorphosed under granulite facies conditions at 1.19 Ga. Iron oxide–apatite and Cu-Ag-Au mineral occurrences occur among gneisses rich in biotite, cordierite, garnet, K-feldspar, orthopyroxene and/or sillimanite-rich gneisses, plagioclase-cordierite-orthopyroxene white gneisses, magnetite-garnet-rich gneisses, garnetites, hyperaluminous sillimanite-pyrite-quartz gneisses, phlogopite-sillimanite gneisses, and tourmalinites. Petrological and geochemical studies indicate that the precursors of these gneisses are altered volcanic and volcaniclastic rocks with attributes of pre-metamorphic Na, Ca-Fe, K-Fe, K, chloritic, argillic, phyllic, advanced argillic and skarn alteration. The nature of these hydrothermal rocks and the ore deposit model that best represents them are further investigated herein through lithogeochemistry. The lithofacies mineralized in Cu (±Au, Ag, Zn) are distinguished by the presence of garnet, magnetite and zircon, and exhibit pronounced enrichment in Fe, Mg, HREE and Zr relative to the least-altered rocks. In discrimination diagrams, the metamorphosed mineral system is demonstrated to exhibit the diagnostic attributes of, and is interpreted as, a metasomatic iron and alkali-calcic (MIAC) mineral system with iron oxide–apatite (IOA) and iron oxide copper–gold (IOCG) mineralization that evolves toward an epithermal cap. This contribution demonstrates that alteration facies diagnostic of MIAC systems and their IOCG and IOA mineralization remain diagnostic even after high-grade metamorphism. Exploration strategies can thus use the lithogeochemical footprint and the distribution and types of alteration facies observed as pathfinders for the facies-specific deposit types of MIAC systems. Full article

A simple and inexpensive thermal oxidation process is used to grow β-Ga₂O₃ oxide (β-Ga₂O₃) thin films/nanorods on a c-plane (0001) sapphire substrate using Ag/Au catalysts. The effect of these catalysts on the growth mechanism of Ga₂O₃ was studied by different characterization techniques, including X-ray diffraction analysis (XRD), Scanning Electron Microscopy (SEM), and Energy Dispersive X-ray analysis (EDX). The XRD results of the grown Ga₂O₃ on a sapphire substrate show three sharp diffraction peaks located at 19.31°, 38.70° and 59.38° corresponding to the $\left(\overline{2}01\right), \left(\overline{4}02\right)$ and $\left(\overline{6}03\right)$ planes of β-Ga₂O₃. Field Emission Scanning Electron Microscope (FESEM) analysis showed the formation of longer and denser Ga₂O₃ nanowires at higher temperatures, especially in the presence of silver nanoparticles as catalysts. Full article

A comparison of two synthesis methods for depositing Au nanoparticles onto TiO₂ was performed: (1) impregnation with HAuCl₄ followed by thermal treatment in argon, and (2) magnetron sputtering from a Au disc. The obtained materials were used for acetaldehyde decomposition in a high temperature reaction chamber and ch aracterised by UV-Vis/DR, XPS, XRD, SEM, and photoluminescence measurements. The process was carried out using an air/acetaldehyde gas flow under UV or UV-Vis LED irradiation. The mechanism of acetaldehyde decomposition and conversion was elaborated by in situ FTIR measurements of the photocatalyst surface during the reaction. Simultaneously, concentration of acetaldehyde in the outlet gas was monitored using gas chromatography. All the Au/TiO₂ samples showed absorption in the visible region, with a maximum around 550 nm. The plasmonic effect of Au nanoparticles was observed under UV-Vis light irradiation, especially at elevated temperatures such as 100 °C, for Au/TiO₂ prepared by the magnetron sputtering method. This resulted in a significant increase in the conversion of acetaldehyde at the beginning, followed by gradual decrease over time. The collected FTIR spectra indicated that, under UV-Vis light, acetaldehyde was strongly adsorbed onto Au/TiO₂ surface and formed crotonaldehyde or aldol. Under UV, acetaldehyde was mainly adsorbed in the form of acetate species. The plasmonic effect of Au nanoparticles increased the adsorption of acetaldehyde molecules onto TiO₂ surface, while reducing their decomposition rate. The increased temperature of the process enhanced the decomposition of the acetaldehyde. Full article

The development of non-noble metal catalysts for gas-phase propylene epoxidation with H₂/O₂ remains challenging due to their inadequate activity and stability. Herein, we report a Cs⁺-modified Ni/TS-1 catalyst (9%Ni-Cs/TS-1), which exhibits unprecedented catalytic performance, giving a state-of-the-art PO formation rate of 382.9 g_PO·kg_cat⁻¹·h⁻¹ with 87.8% selectivity at 200 °C. The catalyst stability was sustainable for 150 h, far surpassing reported Ni-based catalysts. Ni/TS-1 exhibited low catalytic activity. However, the Cs modification significantly enhanced the performance of Ni/TS-1. Furthermore, the intrinsic reason for the enhanced performance was elucidated by multiple techniques such as XPS, N₂ physisorption, TEM, ²⁹Si NMR, NH₃-TPD-MS, UV–vis, and so on. The findings indicated that the incorporation of Cs⁺ markedly boosted the reduction of Ni, enhanced Ni⁰ formation, strengthened Ni-Ti interactions, reduced acid sites to inhibit PO isomerization, improved the dispersion of Ni nanoparticles, reduced particle size, and improved the hydrophobicity of Ni/TS-1 to facilitate propylene adsorption/PO desorption. The 9%Ni-Cs/TS-1 catalyst demonstrated exceptional performance characterized by a low cost, high activity, and long-term stability, offering a viable alternative to Au-based systems. Full article

The use of CH₄ as an energy source is increasing every day. To increase the efficiency of CH₄ combustion and ensure that the equipment meets ecological requirements, it is necessary to measure the CH₄ concentration in the exhaust gases of combustion systems. To this end, sensors are required that can withstand extreme operating conditions, including temperatures of at least 600 °C, as well as high pressure and gas flow rate. ZnGa₂O₄, being an ultra-wide bandgap semiconductor with high chemical and thermal stability, is a promising material for such sensors. The synthesis and investigation of the structural and CH₄ sensing properties of ceramic pellets made from pure and Er-doped ZnGa₂O₄ were conducted. Doping with Er leads to the formation of a secondary Er₃Ga₅O₁₂ phase and an increase in the active surface area. This structural change significantly enhanced the CH₄ response, demonstrating an 11.1-fold improvement at a concentration of 10⁴ ppm. At the optimal response temperature of 650 °C, the Er-doped ZnGa₂O₄ exhibited responses of 2.91 a.u. and 20.74 a.u. to 100 ppm and 10⁴ ppm of CH₄, respectively. The Er-doped material is notable for its broad dynamic range for CH₄ concentrations (from 100 to 20,000 ppm), low sensitivity to humidity variations within the 30–70% relative humidity range, and robust stability under cyclic gas exposure. In addition to CH₄, the sensitivity of Er-doped ZnGa₂O₄ to other gases at a temperature of 650 °C was investigated. The samples showed strong responses to C₂H₄, C₃H₈, C₄H₁₀, NO_2, and H₂, which, at gas concentrations of 100 ppm, were higher than the response to CH₄ by a factor of 2.41, 2.75, 3.09, 1.16, and 1.64, respectively. The study proposes a plausible mechanism explaining the sensing effect of Er-doped ZnGa₂O₄ and discusses its potential for developing high-temperature CH₄ sensors for applications such as combustion monitoring systems and determining the ideal fuel/air mixture. Full article

Internal Dry Reforming of Methane (IDRM) in biogas fed Solid Oxide Fuel Cells (SOFCs) was investigated on Fe-Au modified Ni/GDC electrolyte-supported cells at 900 and 850 °C. The aim was to clarify the synergistic interaction between Fe and Au, focusing on the effect of X wt.% of Au loading (where X = 1 or 3 wt.%) in binary Au-Ni/GDC and ternary 0.5 wt.% Fe-Au-Ni/GDC fuel electrodes. The investigation combined i-V, Impedance Spectroscopy and Gas Chromatography electrocatalytic measurements. It was found that modification with 0.5Fe-Au enhanced significantly the electrocatalytic activity of Ni/GDC for the IDRM reaction, whereas the low wt.% Au content had the most promoting effect. The positive interaction of 0.5 wt.% Fe with 1 wt.% Au increased the conductivity of Ni/GDC and enhanced the corresponding IDRM charge transfer electrochemical processes, especially those in the intermediate frequency region. Comparative long-term measurements, between cells comprising Ni/GDC and 0.5Fe-1Au-Ni/GDC, highlighted the significantly higher IDRM electrocatalytic activity of the modified electrode. The latter operated for almost twice the time (280 h instead of 160 h for Ni/GDC) with a lower degradation rate (0.44 mV/h instead of 0.51 mV/h). Ni/GDC degradation was ascribed to inhibited charge transfer processes in the intermediate frequencies region and to deteriorated ohmic resistance. Stoichiometric analysis on the (post-mortem) surface state of each fuel electrode showed that the wt.% content of reduced nickel on Ni/GDC was lower, compared to 0.5Fe-1Au-Ni/GDC, verifying the lower re-oxidation degree of the latter. This was further correlated to the hindered H₂O production during IDRM operation, due to the lower selectivity of the modified electrode for the non-desired RWGS reaction. Full article

Due to its widespread distribution in industrial, commercial, and residential settings, xylene detection is crucial. In this study, carbon sphere templates and NaHCO₃ etching were used to synergistically prepare WO₃ with uniform macropores, which was then decorated with Au elements. The findings demonstrated that the Au-decorated WO₃-etched sample (WO₃-1%E+Au) had the best sensing performance for 100 ppm xylene (response value: 21.3, optimal operating temperature: 360 °C) and short response/recovery time (1 s/11 s). The etching of NaHCO₃ and the synergistic carbon sphere templates were responsible for the sensing performance, as they enhanced the sample surface’s specific surface area and roughness while also supplying additional active sites. Furthermore, the sensor’s sensitivity and selectivity to xylene were enhanced by the coupling effect and dehydrogenation catalysis of the noble metal Au. The results of this work advance our knowledge of gas-sensing mechanisms and offer guidance for the creation of extremely sensitive and selective xylene gas sensors. Full article

This study examines the impact of Au nanoparticles (Au-NPs) on the chemoresistive gas sensing properties as a function of particle size. The sensing material is composed of ultrathin CuO/Cu₂O films, which are fabricated by either thermal deposition technology or spray pyrolysis. These are used on a silicon nitride (Si₃N₄) micro hotplate (µh) chip with Pt electrodes and heaters. The gas sensing material is then functionalised with Au-NP of varying sizes (12, 20, and 40 nm, checked by transmission electron microscopy) using drop coating technology. The finalised sensors are tested by measuring the electrical resistance against various target gases, including carbon monoxide (CO), carbon dioxide (CO₂), and a mixture of hydrocarbons (HC_Mix), in order to evaluate any cross-sensitivity issues. While the sensor response is markedly contingent on the structural surface, our findings indicate that the dimensions of the Au-NPs exert a discernible influence on the sensor’s behaviour in response to varying target gases. The 50 nm thermally evaporated CuO/Cu₂O layers exhibited the highest sensor response of 78% against 2000 ppm CO₂. In order to gain further insight into the surface of the sensors, a scanning electron microscope (SEM) was employed, and to gain information about the composition, Raman spectroscopy was also utilised. Full article

Mesoporous silica containing Au nanoclusters has been widely used in various fields owing to its desirable properties and functionality. This work introduces a facile method to control the size of Au nanoclusters within silica hosts. This was achieved by applying a reducing gas at a controlled temperature to obtain a narrow or broad Au cluster size distribution inside the silica host. The Au nanoclusters and their silica hosts were characterized through X-ray diffraction, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, ultraviolet-visible spectroscopy, N₂ sorption analysis, and X-ray photoelectron spectroscopy. The average size of the Au nanoclusters was 1.3 nm in the narrow-distribution sample. In comparison, the wide-distribution sample exhibited two cluster populations: 1–2 nm inside the pores and 5–30 nm outside the pores. Methylene blue (M.B.) photocatalysis was conducted under direct sunlight to evaluate the catalytic activity of these materials. Sample 1–Au–SBA-11, containing Au clusters averaging 1.3 nm, achieved substantial M.B. degradation within 90 min—half the time required by the 2–Au–SBA-11 sample. Such Au clusters of different size ranges have potential applications across diverse fields. Full article

Ammonia (NH₃) represents a promising zero-emission fuel in hydrogen fuel cells. Membrane reactors for NH₃ decomposition based on Pd-alloys have demonstrated high NH₃ conversion, high hydrogen diffusivity, and high hydrogen selectivity, which allows for the production of high-purity H₂ without the need for gas separation or purification. However, it is observed that Pd-alloy membranes are to a various degree prone to H₂ flux inhibition in the presence of NH₃. Hence, finding proper means to tailor the surface adsorption properties through, e.g., alloying is imperative to further improve the technology. In the current work, hydrogen and ammonia co-adsorption phenomena on M(1 1 1) and Pd₃M(1 1 1) (M = Pd, Ru, Ag, Au, Cu) surfaces are studied using density functional theory calculations. It is shown that the surface adsorption properties are strongly dependent on the surface composition, which can be linked to the corresponding electronic structure at the membrane surface. Full article

When a star is born, a protoplanetary disk made of gas and dust surrounds the star. The disk can show gaps opened by different astrophysical mechanisms. The gap has a wall emitting radiation, which contributes to the spectral energy distribution (SED) of the whole system (star, disk and planet) in the IR band. As these newborn stars are far away from us, it is difficult to know whether the gap is opened by a forming planet. I have developed RHADaMAnTe, a computational astro code based on the geometry of the wall of a gap coming from hydrodynamics 3D simulations of protoplanetary disks. With this code, it is possible to make models of disks to estimate the synthetic SEDs of the wall and prove whether the gap was opened by a forming planet. An implementation of this code was used to study the stellar system LkCa 15. It was found that a planet of 10 Jupiter masses is capable of opening a gap with a curved wall with a height of 12.9 AU. However, the synthetic SED does not fit to Spitzer IRS SED (${\chi }^2$∼4.5) from $5\mathsf{\mu }$m to $35\mathsf{\mu }$m. This implies that there is an optically thin region inside the gap. Full article

This study introduces a microwave-assisted technique for extracting critical minerals from LED electronic waste. The process begins with microwave irradiation, which thermally decomposes the LED’s plastic lens into a brittle, charred residue. During this stage, the LED chip undergoes deflagration—being rapidly ejected from the reflective cavity and becoming embedded within the decomposed lens material. Consequently, the chip is encapsulated in the resulting charred residue. This composite, consisting of the charred lens and the LED chip, can be easily separated from the metallic pins (Fe, Ni, Ag), which remain almost undamaged. Subsequent calcination of the charred material in air exposes the materials making up the LED chip, which contain critical metals (e.g., Ga, As, In, Y, Au). These metals are then extracted through a two-step acid leaching process involving aqua regia followed by hot concentrated hydrochloric acid, yielding them in potentially recoverable forms. The synergistic effect of microwave irradiation and acid treatment achieves an average extraction efficiency of 96% for critical metals. Notably, this approach enables complete and loss-free recovery of the LED chip, offering a practical and efficient solution for LED e-waste recycling. Full article

Polyethylene imine (PEI) is a synthetic water-soluble and nitrogen-rich polymer with an ethylene amine repeating unit. It exists in a linear or branched forms and finds applications in various areas. PEI is often chemically modified by crosslinking reactions using molecular and polymeric crosslinkers (e.g., trichlorotriazine, epichlorohydrin, ethylene glycol diglycidyl ether, poly(ethylene glycol) diglycidyl ether, etc.) to increase its stability and reduce its water solubility. PEI (pristine/crosslinked) has a strong affinity for metal cations (e.g., Cu²⁺, Au³⁺, Pb²⁺, etc.), where the nitrogen atoms interact with the metal ions, and hence is suitable to remove metals from water with high efficiency. A thin film of crosslinked PEI on substrates can be prepared and finds diverse applications such as in removing metals and dyes, and biofouling prevention in the marine environment. The copper ion, as an example, can be stored (adsorbed) in a thin film of crosslinked PEI on a carbon cloth substrate, which can be released to water by passing an electric current through the film or with an acid treatment. It has also been reported that crosslinked PEI and composite materials can be used for the adsorption of dyes and gases such as CO₂ and SO₂ from the environment. The performance of pristine/composite/crosslinked PEI in gas, metal ion, and dye adsorption is affected by several factors. The focus of this review is to discuss the different reactions used to crosslink PEI and review the properties of the crosslinked materials and their applications. Studies have shown that the properties of the crosslinked PEI and hence its success in capturing metal ions, dyes, and CO₂ is dependent not only on the type of crosslinker but also on the degree of crosslinking. Full article

Chelidonium majus L. is a species with a wide medicinal use, commonly found in anthropogenically degraded habitats, forest edges, and urban parks. This study aimed to determine the chemical composition of the leaves, stems, and roots of Ch. majus and the soil in its rhizosphere in terms of the content of the main elements (Fe, Ca, P, Mg, Al, Na, K, S), trace elements and rare earth minerals (Ti, Mo, Ag, U, Au, Th, Sb, Bi, V, La, B, W, Sc, Tl, Se, Te, Ga, Cs, Ge, Hf, Nb, Rb, Sn, Ta, Zr, Y, Ce, In, Be, and Li), and their comparison in the parts analyzed. The study was conducted in five urban parks in southern Poland in a historically industrialized area. The results showed that Ca has the highest content among the macroelements. Its leaf content ranges from 24,700 to 40,700 mg·kg⁻¹, while in soil, it ranges from 6500 to 15,000 mg·kg⁻¹. In leaves, low values of Al (100–500 mg·kg⁻¹) and Na (100 mg·kg⁻¹) were found in comparison to the other elements tested, while high values of Al (5100–9800 mg·kg⁻¹) were found in soils. Among the macroelements in the Ch. majus stems, K showed the highest concentration (>100,000 mg·kg⁻¹), while the Ca content was 3–4 times lower in the stems than in the leaves. Rhizomes of Ch. majus accumulate the most K and Ca, in the range of 22,800–29,900 mg·kg⁻¹ and 5400–8900 mg·kg⁻¹, respectively. Fe and Al in all locations have higher values in the soil than in the tissues. In turn, the content of Ca, P, Mg, K, and S is higher in plants than in the soil. Determining the elemental content of medicinal plants is important information, as the plant draws these elements from the soil, and, at higher levels of toxicity, it may indicate that the plant should not be taken from this habitat for medicinal purposes. Full article