Search Results (964)

This study investigates the durability of silicone-based membranes in contact with hempcrete under combined moisture and temperature exposure. Membrane specimens were aged in contact with non-treated and treated hempcrete under dry and wet conditions at temperatures up to 90 °C. The evolution of chemical, thermal, and microstructural properties was characterized using FTIR, TGA, DSC, optical microscopy, and SEM–EDS analyses. Results show that dry exposure does not induce measurable changes in membrane structure or performance, confirming that temperature alone is not a critical degradation factor. In contrast, wet exposure leads to significant chemical, thermal, and microstructural changes in the membrane, including degradation of the siloxane network, reduced polymer chain mobility, and the formation of calcium-rich mineral deposits at the interface. These results indicate that membrane degradation is governed by a coupled moisture–ion mechanism involving ion transport, mineral deposition, and hydrolysis of the polymer network. Fiber treatment slightly reduces the aggressiveness of the leachate but does not prevent degradation under wet conditions. Overall, moisture availability and leachate chemistry are identified as key factors controlling the durability of silicone membranes in contact with bio-based materials. Full article

Fire is a key ecological driver in savanna systems, influencing soil biogeochemical processes by releasing nutrients but also causing potential losses through volatilization and leaching. In this study, we investigated how fire seasonality and soil depth influence both Mehlich-3 extractable nutrients and total elemental concentrations. This study was conducted in a long-term fire experiment consisting of 20 plots subjected to seasonal burning treatments (dry season, late dry season, late wet season, and an unburned control). Soil samples were collected from two different depth horizons (0–15 cm and 15–30 cm) and analyzed for nutrient concentrations. We used two-way PERMANOVA, Scheirer–Ray–Hare tests, and non-metric multidimensional scaling (NMDS) to assess treatment effects and interactions. Results showed that fire seasonality did not significantly affect Mehlich-3 extractable nutrients; in contrast, soil depth strongly structured nutrient profiles, with higher concentrations in the upper soil layer, while total elemental concentrations were consistently enriched in the deeper soil horizon. Fire seasonality influenced total elemental nutrient pools, with late dry season burns enhancing potassium and other cations, likely due to combustion of accumulated dry biomass and subsequent ash deposition. Depth effects were particularly pronounced for TN and OC, which were elevated in deeper layers due to the presence of mineral-associated organic matter OM. Our findings highlight that vertical stratification is the dominant control of nutrient distribution, while fire seasonality modulates specific nutrient dynamics. These results underscore the need to incorporate soil profile depth and fire timing when evaluating post-fire soil fertility and ecosystem resilience in savanna landscapes. Full article

Optical fiber sensors deployed in harsh industrial fields, e.g., high-temperature wet-oxygen, face severe challenges in signal attenuation and mechanical degradation. While amorphous silicon oxycarbide (a-SiOC) coatings offer a promising solution due to their adjustable thermo-mechanical properties, balancing their structural density with environmental stability remains a critical technical bottleneck. In this study, a-SiOC coatings were deposited on optical fibers using hexamethyldisilane (HMDS) and trace oxygen via radio-frequency capacitively coupled plasma-enhanced chemical vapor deposition (PECVD). A systematic investigation was conducted to determine the impact of deposition temperature (70–420 °C) on the precursor dissociation kinetics, microstructural evolution, and corrosion resistance of the coatings. An elevation in temperature promotes the elimination of organic terminal groups (–CH₃, –H) and enhances surface diffusion, driving the coating from a loose, carbon-rich “polymer-like” structure (dominated by Si–C bonds) to a dense, inorganic “silica-like” skeleton (dominated by Si–O–Si bonds). High-temperature corrosion tests in a wet-oxygen environment (500–900 °C) demonstrate that the failure mechanism is highly dependent on deposition temperature. Coatings deposited at low temperatures suffer catastrophic cracking due to pronounced oxidative shrinkage and the release of volatile species, whereas coatings deposited at 420 °C exhibit microcracking caused by severe carbon phase separation and stress concentration within the rigid inorganic network. In the present system, 350 °C is identified as the optimal deposition temperature, as it achieves the best balance of network densification and structural flexibility, while exhibiting the best mechanical performance. Full article

Under the pronounced warming–wetting trend in Northwest China, understanding vegetation responses to the redistribution of hydrothermal resources is essential for interpreting regional ecohydrological processes. Here, we developed a bivariate Long Short-Term Memory (LSTM) model to simulate leaf area index (LAI) dynamics for four representative vegetation types (cold temperate forest, shrubland, grassland, and cropland), using air temperature and soil moisture as predictors. The model reproduces seasonal vegetation phenology well across vegetation types (R² > 0.9), indicating that LSTM effectively captures the cumulative and lagged effects of hydrothermal drivers. However, its performance diverges at the interannual scale. Interannual variability in grasslands in water-limited environments is reasonably represented (R² = 0.31), consistent with their sensitivity to short-term hydroclimatic variability under warming–wetting conditions. In contrast, the model fails to reproduce the observed long-term greening trend in forests when driven solely by hydrothermal variables. This contrast suggests distinct underlying mechanisms across ecosystem types. Grassland dynamics are closely linked to high-frequency hydroclimatic variability, whereas forest growth appears to be governed by slower processes and low-frequency drivers, including CO₂ fertilization, nitrogen deposition, and ecological inertia. As a result, hydrothermal variables alone are insufficient to explain long-term forest dynamics. Overall, these findings highlight a transition from water-limited to energy- and process-limited controls across vegetation types and underscore the limitations of purely climate-driven models. Integrating biogeochemical processes or process-based constraints into machine learning frameworks may therefore be necessary to improve predictions of long-term vegetation change under climate change. Full article

The organic complexation of Cu²⁺ in aquatic systems dominates its chemical speciation, affecting its reactivity and bioavailability. Using voltammetry, we investigated Cu²⁺ organic complexing capacity (CuCC) in atmospheric samples, including water-soluble aerosol fraction, rainwater (wet-only deposition), and bulk deposition (wet and dry deposition), collected in a coastal marine area (National Park Brijuni, Adriatic Sea). The focus was on minimizing analytical interferences from surface-active substances (SAS) that accounted for up to 56% of dissolved organic carbon. Method optimization was performed using model SAS (humic-like substances, fulvic acid, and pollen-derived organic material), resulting in an optimal desorption potential of −1.4 V and the addition of 1 mg/L Triton X-100. Under these conditions, CuCC parameters of average ligand concentration and conditional stability constant of (209.8 ± 6.7) nM and log K = (10.2 ± 0.6) in water-soluble aerosol fraction, (117.1 ± 5.0) nM and log K = (9.6 ± 0.2) in rainwater, and (142.9 ± 4.1) nM and log K = (10.2 ± 0.2) in bulk deposition were determined. Atmospheric inputs represented a source of weak Cu-binding ligands for marine areas. In conclusion, short-term monitoring provided insight into the variability of different atmospheric inputs and offered a methodological basis for future long-term, more comprehensive studies. Full article

During wet deposition, particulate matter and gaseous species in the atmosphere are ultimately transported to the Earth’s surface via precipitation and subsequently incorporated into terrestrial ecosystems. Therefore, investigating the fluxes, chemical compositions, and source apportionment of regional wet deposition is of great scientific importance. An analysis of the concentrations, deposition fluxes, spatiotemporal variations, and source apportionment of water-soluble ions in wet deposition can further enhance our understanding of the water-soluble ion characteristics, atmospheric pollution profiles, and potential ecosystem impacts of wet deposition in the Yangtze River Delta and Pearl River Delta regions. Coastal cities in China are most developed regions, and also areas suffering from severe air pollution. This study investigates the chemical characteristics, sources and wet deposition fluxes of water-soluble inorganic ions in precipitation in two typical coastal urban agglomerations of China: Ningbo in the Yangtze River Delta and Guangzhou in the Pearl River Delta. Precipitation samples were collected and analyzed to determine the concentrations of major ions. The results revealed distinct ionic compositions between the two regions. In Ningbo, NO₃⁻ and SO₄²⁻ were the predominant ions accounting for 16.98% to 23.22% of the total, reflecting the influence of anthropogenic emissions from fossil fuel combustion and mobile sources with the NO₃⁻/SO₄²⁻ ratio of 0.90 and 0.70. In Guangzhou, precipitation was characterized by high contributions of SO₄²⁻, NO₃⁻, NH₄⁺, and Ca²⁺, accounting for 17.22% to 23.29% of the total, indicating a mixed influence of industrial emissions, agricultural activities, and construction dust with the NO₃⁻/SO₄²⁻ ratio of 0.92 and 0.87. A clear inverse relationship between rainfall amount and ion concentration was observed at all sites (p < 0.05), demonstrating a significant dilution effect. Seasonality played a crucial role in deposition fluxes. In Ningbo, fluxes peaked during summer from 4667 to 5156 mg·m⁻², while in Guangzhou, distinct dry and rainy season patterns influenced the scavenging efficiency of different ion species. Urban sites exhibited enhanced scavenging of crustal and anthropogenic ions (e.g., Ca²⁺, NH₄⁺) during the rainy season, whereas the coastal site showed elevated fluxes of marine-derived ions (Na⁺, Cl⁻, Mg²⁺, SO₄²⁻) during the same period. The observed trends in ion fluxes suggest a gradual improvement in regional air quality over the study period. These findings elucidate the complex interactions between anthropogenic activities, natural sources, and meteorological factors in shaping the wet deposition chemistry in coastal urban environments, providing essential data for developing regional deposition models and assessing the ecological impacts of atmospheric pollution. Full article

Metasurfaces, planar structures made on a subwavelength scale, enable state-of-the-art manipulation of light and have become a promising solution for compact optical devices. However, fabrication of these nanoscale structures relies on demanding processes, limiting their integration into diverse structures, including three-dimensional ones. In this study, we develop a manufacturing and transfer technique that renders the manipulation and deposition of metasurfaces achievable with high freedom by embedding the nanostructure into a flexible polymer matrix. A metasurface consisting of a TiO₂ nanoparticle array fabricated by nanoimprint lithography was encapsulated within a poly(methyl methacrylate) (PMMA) layer through spin-coating. The layer containing the metasurface was then detached from the original SiO₂ substrate using wet-etching, becoming a free-standing soft sheet carrying nanostructures that can be transferred onto various surfaces. After the transfer, the layer thickness was further tuned through reactive ion etching to modulate the optical response. Incident-angle-resolved transmittance exhibited no significant change in optical bands before and after transfer, confirming that the nanostructure, as well as the photonic band, was well preserved. Thickness reduction of the PMMA cladding induced a clear optical resonance shift, demonstrating controllability of the optical response. This approach provides a versatile route for the installation of metasurfaces and expands the design possibilities for nanophotonic devices. Full article

The purpose of this work was to synthesize and study catalytic systems based on a carbon-containing support obtained from coke fines from the Shubarkol deposit as a waste product of the coal industry for the processing of phenolic compounds. Based on the obtained carbon sorbent, mono- and binary catalysts with active phases of transition metal oxides (Fe, Co, Ni) were synthesized by wet impregnation, followed by heat treatment at 500–700 °C, as well as the aluminum oxide compositions. The surface morphology and elemental composition of the samples were studied by scanning electron microscopy (SEM) with energy dispersion analysis and elemental mapping (EDS mapping), and the content of active phases was determined using inductively coupled plasma optical emission spectrometry (ICP-OES). The catalytic activity was studied in phenol hydrogenation reactions. The CoO/C catalyst demonstrated the greatest activity, providing a 62.36% benzene yield during phenol hydrogenation. The catalytic activity of the CoO/C catalyst has also been studied in the hydrogenation reactions of structurally and functionally more complex compounds, pyrocatechol and resorcinol. The yield of benzene was 63.16% in the hydrogenation of pyrocatechol and 48.64% in the hydrogenation of resorcinol. It was found that the CoO/C catalyst exhibits the highest efficiency at a temperature of 420 °C, a pressure of 6–6.5 MPa and a reaction duration of 120 min. The results obtained make it possible to evaluate the prospects of using a carbon sorbent obtained from coke fines from the Shubarkol deposit as a support for CoO as part of an active and stable catalytic system designed for deep processing of phenolic compounds. Full article

In the present paper, In₂O₃ NPs were synthesized by a wet-chemical method, in the absence and presence of the surfactant, and deposited as thin films on silicon substrates. After deposition, the films were subjected to rapid thermal annealing (RTA) at 550 °C, 750 °C, and 900 °C, for 300 s, under an inert atmosphere. The correlation between the morphological, structural, and optical characteristics, the wetting capacity of In₂O₃ films synthesized under different synthesis conditions, and the influence of the RTA treatment are presented. The vibrations of In-O bonds for In₂O₃ samples were confirmed using FTIR spectroscopy. Structural analysis shows that In₂O₃ NPs have a cubic crystalline structure, but with the increase in temperature at 900 °C, diffraction peaks characteristic of the tetragonal phase of indium appear, correlated with a decrease in lattice parameters, as a result of the crystallinity. The morphology of the In₂O₃ samples was studied by SEM, revealing predominantly spherical and uniformly distributed particles with nanometric sizes. The absorption spectra of the In₂O₃ NPs showed peaks in the ultraviolet region, and the high energy bandgap value of the In₂O₃ films varied between 3.28 and 4.33 eV, depending on the samples and RTA treatment. The contact angle measurements of In₂O₃ films determined the wetting capacity of the surface, reflecting changes in surface morphology and structure induced by the RTA process. The results suggest that In₂O₃ thin films with spherical nanoparticles, good wettability, and percolation can be used for the development of sensors with increased selectivity and sensitivity. Full article

Stone heritage deteriorates through physical, chemical, and biological processes driven by water, climate, and microbial colonization. Multifunctional polymeric coatings combining hydrophobic and antimicrobial moieties have emerged as a promising conservation strategy, yet a substantial gap remains between laboratory innovation and real-world performance. This review critically examines advances from 2021 to 2026, covering wetting theory, antimicrobial mechanisms, and material architectures, including molecularly integrated systems, Sol–Gel hybrids, nanocomposites, and layered systems. Long-term studies on the Aurelian Walls in Rome and stone in Reims show that biocidal efficacy typically declines within one to two years despite the chemical persistence of the coatings. In parallel, hydrophobic performance often deteriorates over time due to UV exposure, particulate deposition, and surface chemical changes, leading to increased wettability and reduced protective efficiency. Substrate porosity governs durability and visual compatibility (ΔE* < 5 threshold), while treatments can reshape microbial communities, favoring stress-tolerant meristematic fungi. Regulatory pressure on fluorinated compounds drives the development of more sustainable alternatives. Emerging directions include stimuli-responsive systems, self-healing materials, slippery interfaces, and precision polymer architectures. However, future progress will depend on tailoring formulations to major lithotypes, improving compatibility with porous substrates, and validating performance through standardized accelerated aging and multi-year field trials. Bridging laboratory design with environmental exposure data and conservation practice will be essential for achieving durable and culturally acceptable protection strategies. Full article

Powder bed fusion (PBF) and directed energy deposition (DED) additive manufacturing use feedstock powders that contain metals associated with skin diseases. We performed a survey of surface contamination and limited task-based dermal exposure assessment (four employees) at a PBF and DED facility. Skin wipes of wrists for two employees in the PBF room had higher post-task levels of chromium, cobalt, molybdenum, and nickel. Personal clothing worn by PBF employees showed evidence of contamination with metals as did personal protective equipment (PPE). Microscopy analysis documented contamination of metals throughout most areas of the facility. Levels of metals on surfaces throughout the facility were (ng/cm²) <5.0–7247 (aluminum), <0.2–4899 (chromium), <background-6.0 (chromium VI), 0.03–468.1 (cobalt), 1.6–100.0 (copper), 32.9–19,000 (iron), 0.01–789.0 (molybdenum), 0.1–12,058 (nickel), 0.1–482.8 (titanium), and 0.07–9.3 (vanadium). Levels were significantly lower in administrative areas compared with the production area but generally did not differ among powder handling and non-powder handling rooms in production. The small number of participants in the dermal exposure assessment and uniqueness of the facility might limit generalizability of the results. At least for this facility, steps to lower skin contact with metals can include washing, consistent use of PPE, and increasing awareness of dermal hazards among workers. Approaches to reduce migration of metals throughout a facility can include using adhesive (“tacky”) mats and boot covers and frequent wet cleaning of floors, tools, handles, and high touch surfaces. Full article

Groundwater sustains human activity in arid crystalline terrains where surface water is scarce and hydrogeological data are limited. However, most groundwater potential mapping approaches depend on deterministic weighting methods without quantifying model variability. This study describes an uncertainty-aware Remote Sensing and Geographic Information Systems (RS–GIS) framework to delineate groundwater potential zones in the Wadi Arab Watershed, Northeastern Sudan. Nine thematic factors—geology and lithology, rainfall, slope, drainage density, lineament density, soil, land use/land cover, topographic wetness index, and height above nearest drainage—were integrated using the Analytical Hierarchy Process (AHP), with acceptable consistency (Consistency Ratio (CR) < 0.1). To address subjectivity in weights, a Dirichlet-based Monte Carlo simulation (500 iterations) was implemented to perturb AHP weights whilst preserving compositional constraints. The resulting Groundwater Potential Index (GWPI) classified 32.69% of the watershed as high to very high potential, primarily associated with alluvial deposits and fractured crystalline rocks. Model validation using Receiver Operating Characteristic (ROC) analysis yielded an Area Under the Curve (AUC) of 0.704, indicating acceptable predictive performance. Uncertainty assessment showed low spatial variability (mean standard deviation (SD) = 0.215) and stable exceedance probabilities, verifying the robustness of predicted high-potential zones. The proposed probabilistic AHP framework augments decision reliability and provides a transferable, cost-effective tool for groundwater planning in data-limited arid basement environments. Full article

Single-atom nanozymes (SANs) with atomically dispersed metal sites show great potential in small biomolecule detection. This review first summarizes SAN synthesis (wet chemistry, atomic layer deposition, etc.), structural features (tunable coordination, metal-carrier interactions), and catalytic mechanisms (synergistic effects, d-band modulation). Afterwards, this review focuses on the applications of SANs in detecting small biomolecules, including glucose, glutathione, uric acid, ascorbic acid, hydrogen peroxide, and dopamine via colorimetry, fluorescence, and electrochemistry. Challenges such as matrix interference and stability, along with future directions in flexible electronics and clinical translation, are discussed, aiming to advance SAN-based detection technologies. Full article

Nanoparticle powders of a Ce_1−xRu_xO₂ mixed oxide (3.0% w/w), were synthesized to be used as catalytic supports, on which Pt and Ir nanoparticles were deposited as the active phase. The catalytic supports were prepared through a route involving microwave heating, while the Pt or Ir nanoparticles were incorporated via the wet incipient method. The {Pt, Ir/Ce_1−xRu_xO₂} catalytic systems were successfully tested as catalysts for low-temperature CO oxidation. To provide adequate support to our results, the compounds were characterized by SEM, EDS, XRD, DRS-UV-vis, and XPS techniques. In addition, BET isotherms were carried out to determine specific surface area features. The CO oxidation evolution was tested in the range of 25–350 °C. Both Pt and Ir supported Ce_1−xRu_xO₂ catalysts that remarkably improved the CO oxidation, reaching and sustaining 100% conversion from 125 °C onwards. Remarkably, the mixed oxide support, by itself, showed outstanding performance, achieving 100% conversion to CO₂, at a temperature of 225 °C. Full article

Rare earth elements (REEs), as significant associated resources in sedimentary phosphate deposits, are commonly processed via the conventional hydrochloric acid wet-process phosphoric acid route (IMI process). In this method, phosphate and rare earth elements are typically leached simultaneously, which subsequently complicates their separation. In this study, a dolomitic rare earth-bearing phosphate concentrate from the Zhijin region of Guizhou Province was selected as the research subject. A stepwise phosphorus-prioritized leaching process was proposed, whereby precise regulation of hydrochloric acid dosage and reaction temperature enabled the preferential leaching of phosphorus (91.27%) and the directed enrichment of rare earth elements in the leaching residue (enrichment ratio of 4.7), thereby achieving efficient phosphorus–rare earth separation at the source. Subsequent process mineralogical analyses of the phosphate concentrate and the leaching residue revealed that rare earth elements occur in fluorapatite predominantly through isomorphic substitution. Following preferential phosphorus leaching, the residual Ca combines with F to form CaF₂, while rare earth elements become concentrated within the leaching residue. Finally, kinetic investigations and response surface analyses demonstrated that the preferential phosphorus leaching process is governed by diffusion through the solid product layer. Among the influencing factors, hydrochloric acid dosage (A), leaching temperature (C), and the interactions between leaching time and the solid–liquid ratio (B, D) were identified as the most significant parameters affecting phosphorus leaching efficiency. This study elucidates, from a mechanistic perspective, the governing principles of phosphorus dissolution and rare earth enrichment within the hydrochloric acid preferential leaching system, thereby providing important theoretical support and technical guidance for simultaneously achieving efficient phosphorus extraction and targeted rare earth enrichment within the hydrochloric acid wet-process phosphoric acid production route. Full article