Search Results (3,203)

In recent decades, photocatalysis has received huge attention as a way to address the main environmental challenges affecting planet Earth. Among these, the control of CO₂ emission and its concentration in the atmosphere, as one of the greenhouse gases causing global warming, is of primary importance. This study focuses on the hydrothermal preparation of doped Ba and Ca-based titanates as efficient photocatalytic materials for CO₂ photoreduction under solar light. The materials were characterized by SEM-EDX, XPS, FT-IR ATR, DRS, CHNS, XRD, and N₂ physisorption analyses, and tested for gas-phase methane production from the target reaction. According to the results, the visible light harvesting properties were significantly improved with C and N doping, where glucose and a bio-based chitosan acted as the C and C+N sources, respectively. In particular, C-Ba-based titanate (CBaT) indicated the highest CH₄ productivity, 2.3 µmol/g_cat, against zero activity of the corresponding bare titanate structure, BaT. The larger surface area and pore volume, as well as its narrower band gap, are suggested as the major reasons for the promising performance of CBaT. This work provides new insights for the facile fabrication of efficient photoactive perovskite materials with the aim of CO₂-to-CH₄ photoreduction under solar light. Full article

Natural gas (NG) engine catalysts face unique challenges in emission control due to their distinct raw emission characteristics. This study investigates the exhaust conversion and by-product generation of a Palladium-based catalyst of an NG engine through small-sample catalyst experiments, mainly focusing on the effect of feed gas composition on the conversion efficiency and N₂O/NH₃ emissions. Results show that N₂O is generated via NO reduction by H₂ (80~275 °C) and CO (275~400 °C) in the temperature range of 80~400 °C. NH₃ generation occurs at 175~550 °C, mainly via NO reduction by H₂ (supplied from the water–gas shift (WGS) reaction) and CO below 425 °C and exclusively by H₂ (supplied from the steam reforming (SR) reaction) above 425 °C. An increase (0.9705~1.0176) in lambda enhances CO and CH₄ conversion while reducing N₂O and NH₃ emissions, but it inhibits NO conversion and promotes NO₂ formation. A lambda of 0.9941 achieves high conversion efficiency (≥90%) for CO, CH₄, and NO, with reduced N₂O and zero NH₃ emissions. An increase in H₂O (8~16%) accelerates the WGS and SR reactions, improving pollutant conversion. However, it aggravates N₂O and NH₃ emissions, with peak levels rising by 54% and 31%, respectively. Increased H₂ (500~1500 ppm) preferentially consumes NO and reversely shifts the equilibrium of the WGS and SR reactions, reducing CO and CH₄ conversion while improving NO conversion. And it promotes N₂O selectivity at high temperature and NH₃ selectivity at low temperature and peak emissions, with peak concentrations increasing by 58% and 15%, respectively. These findings reveal the by-product formation mechanism in the catalyst, providing valuable insights for the emission control of NG-fueled engines. Full article

High levels of dissolved salts in irrigation water sources limit melon cultivation in northeastern Brazil. In this context, nitrogen fertilization has been employed as one strategy to alleviate the effects of salt stress on plants. This study aimed to evaluate the effect of different nitrogen sources on cantaloupe melon cultivation under fertigation and irrigation with water of the same salinity and different cationic concentrations (Na⁺ and Ca⁺). The research consisted of two experiments, each following a randomized complete block design in a 4 × 2 factorial arrangement with four replicates. The treatments included four levels of electrical conductivity of the nutrient solution (2.0; 3.0; 4.0; and 5.0 dS m⁻¹) and two nitrogen sources of different origins: NO₃⁻ [Ca(NO₃) and KNO₃] and NH₄⁺ [CH₄N₂O and NH₄H₂PO₄]. The following factors were chlorophyll pigments, chlorophyll a fluorescence, and fruit weight. Nitrogen fertilization with NH₄⁺ mitigated salt stress by increasing the synthesis of chlorophyll a and carotenoids in plants irrigated with NaCl-based saline water. Furthermore, there was no influence of nitrogen sources on chlorophyll a fluorescence. Finally, NO₃⁻ fertilization reduced the effects of salt stress on the leaf mass ratio, specific leaf area under Ca²⁺ fertigation, and relative growth rate of leaf area in melons under cationic prevalences of Na⁺ or Ca²⁺ (associated with Cl⁻). Full article

Static chambers combined with isotopic (δ¹³C and δ¹⁸O) and flux (CO₂ and CH₄) measurements were applied, to explore the effects of mosses and long-term nitrogen (N) addition at two levels (22.5 and 45 kg N ha⁻¹ yr⁻¹) on δ¹³C and δ¹⁸O values of respired CO₂ across three autumn seasons under a temperate forest (northeastern China) and their relationships with CO₂ and CH₄ fluxes and with soil properties. Mosses generally depleted δ¹³C and enriched δ¹⁸O in respired CO₂, likely by altering soil microenvironments or/and substrate use. The effect of N addition on the δ¹³C and δ¹⁸O values of respired CO₂ varied with years, and its interaction with mosses had no effects on the isotopic values. The removal of mosses decreased CO₂ fluxes and the addition of N at a high dose increased CH₄ fluxes. The δ¹³C and δ¹⁸O values of respired CO₂ decreased at soil moisture levels below and above an optimum, and the moisture-dependent effect became more pronounced for the δ¹⁸O than for the δ¹³C. The results of structural equation modeling showed that 70% of the variability of δ¹³C values of respired CO_2. was accounted for by the N addition, mosses, soil moisture, and CH₄ and CO₂ fluxes, while only 22% of the variability of δ¹⁸O values of respired CO₂ was explained by these factors. The results highlight that moss–soil interaction drives the isotopic shifts, which is modulated by N availability. Soil moisture regulates the δ¹⁸O values of respired CO₂, but its drivers remain poorly understood. Future work should target processes influencing the δ¹⁸O shifts of respired CO₂ and deep soil property interactions. Full article

Tropaeolum tuberosum (mashua) is a native Andean tuber recognized for its high nutritional and bioactive compound content. Among the various morphotypes, the black and yellow variants show potential differences in composition and functionality. This study aimed to compare the thermo-energetic, nutritional, and physicochemical characteristics of two morphotypes (black and yellow) of Tropaeolum tuberosum flour from the Peruvian Andes. Flours were obtained from tubers harvested in Ayacucho, Peru, and analyzed using elemental analysis for carbon, hydrogen, nitrogen, and sulfur (CHNS), inductively coupled plasma optical emission spectrometry (ICP-OES), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and bomb calorimetry. The empirical formula is CH_1.74O_0.91N_0.06S_0.005 for black mashua and CH_1.78O_0.92N_0.05S_0.005 for yellow mashua. Black flour exhibited higher protein (17.6% vs. 14.8%) and fat contents (8.0% vs. 6.7%), along with nearly double the iron content. Both flours showed similar starch granule morphology and gelatinization enthalpy (~2 J/g), but the black flour had higher gelatinization temperatures. Calorimetric analysis revealed a greater net calorific value (qNCV) in black mashua flour (4157 ± 22 kcal/kg) than in yellow flour (4022 ± 19 kcal/kg). The thermogravimetric profiles indicated good thermal stability with approximately 30% residual mass. These findings suggested that black mashua flour possesses superior nutritional and energy characteristics, supporting its application in functional food formulations and energy-rich gluten-free products. Full article

The electrochemical oxidation of anodic metal (cobalt, nickel, zinc or cadmium) in a cell containing an acetonitrile solution of the ligand (E)-N-(2-(((2-hydroxynaphthalen-1-yl)methylene)amino)phenyl)-4-methylbenzenesulphonamide (H₂L) affords complexes with the general formula [ML] (M = Co, Ni, Zn and Cd). Additionally, it was possible to obtain complexes with the general formula [MLL′] when L′ = 2,2-bipyridine (2,2-bpy), 4,4-bipyridine (4-4′-bpy) or 1,10-phenanthroline (phen) was present in the electrolytic cell. All of the compounds obtained have been characterized via microanalysis, IR spectroscopy, mass spectrometry, UV–visible spectroscopy and, in the case of diamagnetic compounds, via ¹H NMR spectroscopy. Further structural and electronic characteristics of these adducts have been obtained via DFT simulations. The compounds NEt₄[CoL₂] (1), [NiL(H₂O)] (2), [NiL(CH₃CN)(H₂O)]₂ (3), [Ni₂L₂(4,4′-bpy)] (4), [Zn₂L₂(MeOH)₂] (5) and [ZnL(2,2′-bpy)](CH₃CN) (6) have been characterized via X-ray diffraction. In this paper, we present a detailed study of the different behavior of the above-mentioned ligand depending on the metal and/or the presence of ancillary ligands. Full article

Gold mineralisation at Ity (Ivory Coast) is spatially associated with skarns formed at contacts between carbonate-rich Birimian volcano-sedimentary rocks and felsic intrusions, whereas at Dahapleu, a nearby skarn-free prospect, gold occurs in structurally controlled shear zones. Gold occurs as native gold in pyrite or as a Bi–Te–Au–Ag telluride assemblage. Fluid inclusion data indicate that Ity formed through a hybrid model: a mesothermal orogenic gold system dominated by CO₂–CH₄ fluids at >350 °C, superimposed on earlier skarn mineralisation characterised by saline fluids. At Dahapleu, no skarn fluids were identified, but volatile-rich inclusions with more variable signatures (CO₂, CO₂–CH₄, CO₂–N₂) indicate metamorphic fluids circulating in convective, fault-related systems and recording distinct fluid–rock interactions. The Ity–Dahapleu mineralising system thus displays fluid inclusion characteristics typical of mesothermal orogenic gold systems, likely at higher temperatures than most West African Birimian deposits. Overall, the Ity system reflects a long-lived thermal anomaly driving fluid circulation and metal deposition, with successive favourable events: rapid exhumation of hot lithospheric crust, granite intrusion, and skarn formation, followed by shear deformation and hydrothermal activity. Full article

Water scarcity and greenhouse gas (GHG) emissions pose significant challenges to sustainable wheat production in tropical regions such as the Brazilian Cerrado. This study evaluated the effects of different soil water depletion levels, denoted as f (20%, 40%, 60%, and 80% of available water capacity—AWC), on no-tillage winter wheat irrigated after rainfed soybean cultivation. Grain yield decreased significantly at depletion levels ≥ 60%, with the highest yields observed at f = 20% (6933 kg ha⁻¹) and f = 40% (6814 kg ha⁻¹). Water use efficiency (WUE) ranged from 12.4 to 14.0 kg ha⁻¹ mm⁻¹, with no significant differences among treatments. Nitrous oxide (N₂O) emissions peaked at f = 60% (4.55 kg ha⁻¹), resulting in the highest average global warming potential (GWP = 1.185.78 kg CO₂ eq ha⁻¹) and greenhouse gas intensity (GHGI = 192.66 kg CO₂ eq Mg⁻¹ grain). Methane (CH₄) acted as a net sink across all irrigation levels. Soil enzymatic activities (β-glucosidase and arylsulfatase) were not significantly affected by irrigation management. Overall, irrigation scheduling based on f = 40% soil water depletion provided the best balance between productivity and environmental sustainability, representing a climate-smart and resource-efficient strategy for wheat production in tropical agroecosystems. These findings provide promising insights for tropical agriculture by showing that sustainable irrigation can balance productivity and climate mitigation in the Cerrado. Maintaining soil water depletion below 60% significantly reduces N₂O emissions and environmental impact, emphasizing the importance of conservation practices. Additionally, preserving soil biological quality supports the long-term viability of these practices and offers valuable guidance for policies promoting efficient irrigation in climate-vulnerable regions. Full article

CH₄ is a powerful greenhouse gas that is thought to be one of the main causes of global warming. The catalytic conversion of methane in the presence of oxygen into hydrogen-rich syngas, known as the partial oxidation of methane (POM), is highly appealing for environmental and synthetic concerns. In search of a cheap catalytic system, the Ni-supported MgO-based (5Ni/MgO) catalyst and the promotional supplement of 1–3 wt.% Sr over 5Ni/MgO are investigated for the POM reaction. Catalysts are characterized by N₂ sorption isotherm analysis, X-ray diffraction spectroscopy, Raman spectroscopy, temperature-programmed desorption techniques, and thermogravimetry. Increasing the loading of strontium over Ni/MgO induced a strong interaction of NiO with the support, pronouncedly. In the presence of oxygen during the POM, the moderate-level interaction of NiO with the support grows markedly. Overall, at a 600 °C reaction temperature, the 5Ni2Sr/MgO catalyst shows 72% CH₄ conversion (~67% H₂ yield) at 14,400 mL/h/g_cat GHSV and ~86% CH₄ conversion (84% H₂ yield) at 3600 mL/h/g_cat GHSV. Achieving a higher activity towards the POM over cheap Ni, Sr, and MgO-based catalysts might draw the attention of environmentalists and industrialists as a low-cost and high-yield system. Full article

Pyridinecarbonitriles (pyCN), also referred to as cyanopyridines, are promising ligands for the formation of pyridine-based coordination compounds due to their two different N-donor atoms, which enable versatile coordination modes. Copper(II) complexes containing pyCN derivatives are of particular interest for their potential applications in medicinal chemistry and materials science. In this study, the synthesis, structural characterization, and thermal and magnetic properties of three new copper(II) complexes with 3-pyCN, 4-pyCN, and ethyl picolinimidate, obtained in situ by means of alcoholysis of 2-pyCN, are reported: [Cu₂(μ-Ac)₄(3-pyCN)₂] (1), [Cu(H₂O)₂(Etpic)₂]NO₃ (2), and [Cu(NO₃)₂(CH₃CN)(4-pyCN)₂]·CH₃CN (3). Single-crystal X-ray diffraction confirmed that complex 1 features a dinuclear paddle-wheel structure with bridging acetato ligands and monodentate 3-pyCN molecules, coordinated through the ring nitrogen, while complexes 2 and 3 are mononuclear. Thermal analysis showed an intense and highly exothermic decomposition of complex 3, containing nitrate ligands. Magnetic measurements revealed strong antiferromagnetic coupling in the dinuclear complex 1, whereas complexes 2 and 3 displayed paramagnetic behavior with effective magnetic moments ranging from 1.8 μ_B to 2.0 μ_B, consistent with isolated Cu(II) centers. Full article

Forest soil greenhouse gas emissions play a critical role in global climate change. This review synthesizes the mechanisms of temperature change impacts on forest soil greenhouse gas (CO₂, CH₄, N₂O) emissions, the complex response patterns of ecosystems, and existing knowledge gaps in current research. We highlight several critical mechanisms, such as the high temperature sensitivity (Q₁₀) of methane (CH₄) and CO₂ emissions from high-latitude peatlands, and the dual effect of chronic nitrogen deposition, which can cause short-term stimulation but long-term suppression of soil CO₂ emissions. It emphasizes how climatic factors, soil characteristics, vegetation types, and anthropogenic disturbances (such as forest management and fire) regulate emission processes through multi-scale interactions. This review further summarizes the advancements and limitations of current research methodologies and points out future research directions. These include strengthening long-term multi-factor experiments, developing high-precision models that integrate microbial functional genomics and isotope tracing techniques, and exploring innovative emission reduction strategies. Ultimately, this synthesis aims to provide a scientific basis and key ecological threshold references for developing climate-resilient sustainable forest management practices and effective climate change mitigation policies. Full article

Light attenuation and excess handling of light-cured luting agents create problems in bonding veneer restorations. The aim of the present study was to assess the curing capacity of light-cured veneer luting agents (VLA) [Choice 2 (CH2), G-Cem Veneer (GCV), Panavia LC Veneer (PNV), PermaCem LC Veneer (PMS), and Variolink Esthetic LC (VEV)] under lithium disilicate veneers, in the presence or absence of touch-cure primers (Adhese Universal Bond DC for VEV, G Premio Bond + DCA Activator for GCV, and V5 Tooth Primer V5 for PNV) and to evaluate material setting under two tack-curing irradiation modes (contact, distant). The methods used were ATR–FTIR spectroscopy and Vickers hardness (VHN) tests (n = 5/product and test). According to the results, all materials cured under the ceramic demonstrated significantly lower DC% from the controls, with a ranking of VEV, CH2 > GCV, PMS, PNV. The primers improved DC% by 4–13% only in the veneer groups. Tack-curing in contact mode demonstrated conversion and hardness values ranging from 37% to 78% and 31% to 57% of the controls respectively, corresponding to a vitreous state. For the distant mode, very low conversion values were found (0–7% of the controls), with untraceable indentations. It can be concluded that low translucency veneers reduce conversion of VLAs, which can be improved by using touch-cure activators. Tack-curing, as instructed, creates vitrified materials, resulting in difficult removal of set excess, which implies the need for better standardization of the procedure. Full article

This research explores the effect of a composite support of SiO₂ and Al₂O₃ with Fe and Co incorporated as catalysts for Fischer–Tropsch synthesis (FTS) using a 3D-printed stainless steel (SS) microchannel microreactor. Two mesoporous catalysts, FeCo/SiO₂Al₂O₃ and Co/SiO₂Al₂O₃, were synthesized via a one-pot (OP) method and extensively characterized using N₂ physisorption, XRD, SEM, TEM, H₂-TPR, TGA-DSC, FTIR, and XPS. H₂-TPR results revealed that the synthesis method significantly affected the reducibility of metal oxides, thereby influencing the formation of active FTS sites. SEM-EDS and TEM further revealed a well-defined hexagonal matrix with a porous surface morphology and uniform metal ion distribution. FTS reactions, carried out in the 200–350 °C temperature range at 20 bar with a H₂/CO molar ratio of 2:1, exhibited the highest activity for FeCo/SiO₂Al₂O₃, with up to 80% CO conversion. Long-term stability was evaluated by monitoring the catalyst performance for 30 h on stream at 320 °C under identical reaction conditions. The catalyst was initially active for the methanation reaction for up to 15 h, after which the selectivity for CH₄ declined. Correspondingly, the C₄⁺ selectivity increased after 15 h of time-on-stream, indicating a shift in the product distribution toward longer-chain hydrocarbons. This trend suggests that the catalyst undergoes gradual activation or restructuring under reaction conditions, which enhances chain growth over time. The increase in C₄⁺ products may be attributed to the stabilization of the active sites and suppression of methane or light hydrocarbon formation. Full article

In this work, alkylammonium-functionalized hollow mesoporous silica as a nonocarrier of drugs was synthesized to realize enhanced cancer therapy by pH stimuli for sustained drug release. First, functionalized hollow mesoporous silica nanoparticles (Hollow MSNs) were synthesized using dodecyl dimethyl(3-sulfopropyl)ammonium hydroxide (DDAPS), sodium dodecyl sulfate (SDS), and triethanolamine as structure-directing agents, while tetraethyl orthosilicate (TEOS) and N-trimethoxysilypropyl-N,N,N-trimethylammonium chloride (TMAPS) were used as silica sources under basic condition via the sol–gel process. The structure and morphology of the alkylammonium-functionalized hollow mesoporous silica nanoparticles (Hollow MSN-N⁺CH₃) were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N₂ adsorption–desorption analysis, and Fourier transform infrared (FT-IR) spectroscopy. The functionalized hollow MSNs had a particle size of about 450 nm and a shell thickness of about 60 nm with uniform size. The nanoparticle had a surface area of 408 m²g⁻¹, pore volume of 0.8 cm³g⁻¹, and a uniform pore diameter of 45.9 Å. In the cancer cell viability test with a MCF-7 cell, fludarabine-incorporated and alkylammonium-functionalized hollow mesoporous silica nanoparticles (Flu/Hollow MSN-N⁺CH₃) showed excellent cancer cell death comparable with pure fludarabine drug with the controlled drug release by pH stimuli. It is suggested that our current materials have potential applicability as pH-responsive nanocarriers in the field of cancer therapy. Full article

Soils act as sources or sinks for three major greenhouse gases (CO₂, CH₄, and N₂O). Approximately 20% of global CO₂ emissions are released from soils through the soil respiration process. Soil respiration (soil CO₂ emission) can account for over 85% of ecosystem respiration. The aim of this study was to compare managed and unmanaged stands of pedunculate oak (Quercus robur L.) in order to investigate the impact of forest management on soil CO₂ emissions. We selected one managed and two unmanaged stands. The first stand (S1) represents a managed middle-aged stand, which is the optimal stage of development. The second stand (S2) belongs to the over-mature stage of development in an old-growth oak forest, while the third stand (S3) belongs to the decay stage of development in an old-growth oak forest. The closed chambers method was used for air sampling and the air samples were analyzed using gas chromatography (GC). Multiple regression models that include soil temperature (ST), soil moisture (SM), and their interaction provide a better explanation for variation in soil CO₂ emission (SCDE) (higher R² values) compared to regression models that only involve two variables (ST and SM). The study showed that SCDE in the decay stage of old-growth forest (S3) was significantly lower (p < 0.001) compared to the other two stands (S1 and S2). S3 is characterized by very low canopy cover and intensive natural regeneration, unlike S1 and S2. However, there were no significant differences in SCDE between the managed middle-aged stand (S1) and the over-mature (old-growth) stand (S2). Over a long-term rotation period in pedunculate oak forests, forest management practices that involve the periodic implementation of moderate silvicultural interventions can be deemed acceptable in terms of maintaining the carbon balance in the soil. Full article