Search Results (308)

Geothermal energy has been recognized as a promising renewable resource for sustainable power generation; however, the efficiency of conventional geothermal power plants has remained relatively low, and high investment costs have limited their competitiveness with other renewable technologies. In this context, the present study introduced an innovative geothermal electricity generation system aimed at enhancing energy efficiency, cost-effectiveness, and sustainability. Unlike traditional configurations, the system raised the geothermal source temperature passively by employing advanced heat transfer mechanisms, eliminating the need for additional energy input. Comprehensive energy, exergy, and exergoeconomic analyses were carried out, revealing a net power output of 43,210 kW and an energy efficiency of 30.03%, notably surpassing the conventional Kalina cycle’s typical 10.30–19.48% range. The system’s annual electricity generation was 11,138.53 MWh, with an initial investment of USD 3.04 million and a short payback period of 3.20 years. A comparative assessment confirmed its superior thermoeconomic performance. In addition to its technoeconomic advantages, the environmental performance of the proposed configuration was quantified. A streamlined life cycle assessment (LCA) was performed with a functional unit of 1 MWh of net electricity. The proposed system exhibited a carbon footprint of 20–60 kg CO₂ eq MWh⁻¹ (baseline: 45 kg CO₂ eq MWh⁻¹), corresponding to annual emissions of 0.22–0.67 kt CO₂ eq for the simulated output of 11,138.53 MWh. Compared with coal- and gas-fired plants of the same capacity, avoided emissions of approximately 8.6 kt and 5.0 kt CO₂ eq per year were achieved. The water footprint was determined as ≈0.10 m³ MWh⁻¹ (≈1114 m³ yr⁻¹), which was substantially lower than the values reported for fossil technologies. These findings confirmed that the proposed system offered a sustainable alternative to conventional geothermal and fossil-based electricity generation. Multi-objective optimization using NSGA-II was carried out to maximize energy and exergy efficiencies while minimizing total cost. Key parameters such as turbine inlet temperature (459–460 K) and ammonia concentration were tuned for performance stability. A sensitivity analysis identified the heat exchanger, the first condenser (Condenser 1), and two separators (Separator 1, Separator 2) as influential on both performance and cost. The exergoeconomic results indicated Separator 1, Separator 2, and the turbine as primary locations of exergy destruction. With an LCOE of 0.026 USD/kWh, the system emerged as a cost-effective and scalable solution for sustainable geothermal power production without auxiliary energy demand. Full article

This study investigates the effect of temperature on the performance of the single-walled carbon nanotube (SWCNT) film/Si photodetector. Specifically, the photocurrent across a SWCNT/Si heterojunction when illuminated with light of 632.8 nm wavelength of different powers was studied in detail in a wide temperature range, from 20 to 300 K. The objective was to determine the parameters of the heterojunction, which is inherently inhomogeneous, and to identify the main ones that determine the optoelectronic figures of merit of a photodetector based on it. The barrier height and its temperature dependence were determined within the framework of the theory of thermionic emission, taking into account the non-uniform distribution of the barrier height over the heterojunction area. The parameters of the heterojunction and SWCNT/Si interface and their temperature dependences were calculated based on the known temperature dependences of the concentration of charge carriers and ionized impurities in Si using the Poisson equation based on Fermi–Dirac statistics. The obtained results indicate the importance of interplay between the effects of reducing the barrier height and the processes of decreasing the separation efficiency of nonequilibrium charge carriers and increasing the rate of their recombination. Full article

Climate change is a significant driver of antimicrobial resistance (AMR) and infectious disease dynamics, presenting urgent and interconnected global health challenges. Rising temperatures, ecosystem alterations, and extreme weather events amplify the global spread of resistant pathogens, zoonotic infections, and vector-borne diseases. These impacts disproportionately affect low- and middle-income countries (LMICs), escalating healthcare costs and straining limited infrastructure. A critical characteristic of bacterial resistance is that it often does not incur a fitness cost, underscoring the necessity of preventive strategies to mitigate climate-driven AMR emergence, rather than relying on reactive treatments after resistance is established. Climate change accelerates AMR primarily by increasing the prevalence of infectious diseases, which in turn drive higher antibiotic use and select resistance. The socioeconomic consequences are particularly severe in LMICs, where high climate vulnerability converges with weaker health systems. Pandemic-related disruptions provided key insights into environmental dynamics, with notable temporary reductions in nitrogen dioxide (NO₂) emissions, i.e., 20–30% in China, Italy, France, and Spain, and approximately 30% in the USA, which highlights the responsiveness of ecosystems to human activity. Unlike prior reviews that treated AMR and climate change as separate issues, this article integrates mechanistic evidence, epidemiological insights, and global strategies to provide a comprehensive One Health framework addressing these synergistic threats. We conclude that AMR and climate change are interlinked crises requiring urgent, integrated interventions. The quadripartite (FAO, UNEP, WHO, WOAH) provides a crucial framework for the coordinated cross-sectoral strategies, strengthened surveillance, and robust antibiotic stewardship required to mitigate this dual threat and safeguard global health security. Full article

Chemical Looping Combustion (CLC) technology has emerged as a promising approach for carbon capture owing to its CO₂ separation capability, which addresses the pressing challenge of global climate change. Although iron-based oxygen carriers offer economic advantages owing to their abundance and low cost, their limited cyclic stability restricts their industrial deployment. This study focused on optimizing the performance of iron-based oxygen carriers through composite modification with Al₂O₃ and TiO₂. Using Cantera (2.5.0) software and the minimum Gibbs free energy principle, conversion rates and product distributions of Fe₂O₃, Fe₂O₃/Al₂O₃, and Fe₂O₃/TiO₂ were systematically analyzed under varying temperatures (800–950 °C), oxygen carrier-to-fuel molar ratios (O/C = 1–15), and pressures (0.1–1.0 MPa). The optimal conditions were identified as 900 °C, O/C = 8, and 0.1 MPa. After 50 simulation cycles, Fe₂O₃/Al₂O₃ and Fe₂O₃/TiO₂ achieved average total reaction counts of 503 and 543, respectively, substantially exceeding 296 cycles for Fe₂O₃. The results indicated that Al₂O₃ and TiO₂ improved cyclic stability via physical support and structural regulation mechanisms, thereby offering a practical carrier composite modification strategy. This study provides a theoretical basis for the development of high-performance oxygen carriers and supports the industrial application of CLC technology for efficient carbon capture and emission mitigation. Full article

RMB₆-TMB₂ (RM = rare earth elements, TM = transition metal elements) composites retain superior field emission properties of RMB₆ while addressing its inherent mechanical limitations by constructing a eutectic structure with TMB₂. Herein, an in situ route for synthesizing RMB₆-TMB₂ composite nanopowders with homogeneous phase distribution using reduction reactions was proposed. The LaB₆-ZrB₂ composite nanopowders were synthesized in situ for the first time using sodium borohydride (NaBH₄) as both a reducing agent and boron source, with lanthanum oxide (La₂O₃) and zirconium dioxide (ZrO₂) serving as metal sources. The effects of the synthesis temperature on phase compositions and microstructure of the composites were systematically investigated. The LaB₆-ZrB₂ system with a eutectic weight ratio exhibited an accelerated reaction rate, achieving a complete reaction at 1000 °C, 300 °C lower than that of single-phase ZrB₂ synthesis. The composite phases were uniformly distributed even at nanoscale. The composite powder displayed an average particle size of ~170 nm when synthesized at 1300 °C. With the benefit of the in situ synthesis method, LaB₆-TiB₂, CeB₆-ZrB₂, and CeB₆-TiB₂ composite powders were successfully synthesized. This process effectively addresses phase separation and contamination issues typically associated with traditional mixing methods, providing a scalable precursor for high-performance RMB₆-TMB₂ composites. Full article

Ammonia (NH₃) emissions from swine manure pits contribute significantly to odor nuisance, health risks, and secondary PM_2.5 formation. This study assessed the pilot-scale performance of three source-control technologies: surface sealing with surfactant-based foam system (FOAM SYSTEM), swine manure wiping and removing system (WIPING SYSTEM), and belt-conveyor-based solid–liquid separator system (BELT SYSTEM). Each technology targets a different pathway in the ammonia generation process. The FOAM SYSTEM suppresses volatilization by forming a foam barrier at the air–liquid interface. The WIPING SYSTEM reduces precursor contact time by periodically removing feces. The BELT SYSTEM separates feces and urine upon excretion, inhibiting enzymatic ammonia formation. Among the individual systems, the BELT SYSTEM achieved the highest ammonia reduction efficiency of 91.7%, followed by the FOAM SYSTEM (73.6%) and WIPING SYSTEM (64.4%). The combined FOAM SYSTEM + BELT SYSTEM yielded the best performance with an ammonia reduction efficiency of 94.4%, showing modest synergy without operational interference. In contrast, the FOAM SYSTEM + WIPING SYSTEM configuration achieved 71.1%, slightly lower than the FOAM SYSTEM alone, likely due to foam disruption. Environmental sensitivity tests revealed that higher temperatures and alkaline pH elevated NH₃ emissions, whereas systems that maintained near-neutral pH, like the FOAM SYSTEM, demonstrated greater stability. These findings highlight the importance of integrating physical and source-control mechanisms while considering environmental variability for effective on-farm ammonia mitigation. Full article

Platinum has emerged as an optimal catalyst for the selective hydrogenation of nitroarenes owing to its high hydrogenation activity, selectivity, and stability. In this study, we report the fabrication of platinum nanoparticles stabilized on a composite support consisting of gum acacia polymer (GAP) and TiO₂. It was engineered for the targeted reduction of nitroarenes to arylamines via selective hydrogenation in methanol at ambient temperature. The non-toxic and biocompatible properties of GAP enable it to act as a reducing and stabilizing agent during synthesis. The synthesized nanocatalyst was characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Morphological and structural analyses revealed that the fabricated catalyst consisted of minuscule Pt nanoparticles integrated within the GAP framework, accompanied by the corresponding TiO₂ nanoparticles. Inductively coupled plasma optical emission spectrometry (ICP-OES) was employed to ascertain the Pt content. The mild reaction conditions, decent yields, trouble-free workup, and facile separation of the catalyst make this method a clean and practical alternative to nitroreduction. Selective hydrogenation yielded an average arylamine production of 97.6% over five consecutive cycles, demonstrating the stability of the nanocatalyst without detectable leaching. Full article

Thermal camouflage technologies manipulate heat fluxes to conceal objects from thermographic detection, offering potential solutions for thermal management in high-power-density electronics. Most reported approaches are aimed at scenarios where the target is not a heat source; however, any target with a non-zero temperature emits thermal radiation described by the Stefan–Boltzmann law since the thermal radiation of an object is proportional to the fourth power of its temperature (T⁴). To address this issue, this study proposes a thermal camouflage device that considers the influence of radiative thermal transfer from the target. The underlying principle involves maintaining synchronous heat transfer separately along both the device and background surfaces. Numerical simulation confirms the feasibility of this proposed thermal camouflage strategy. Moreover, by altering some parameters related to the target such as geometry, location, temperature, and surface emissivity, excellent performance can be achieved using this device. This work advances thermal management strategies for high-power electronics and infrared-sensitive systems, with applications in infrared stealth, thermal diagnostics, and energy-efficient heat dissipation. Full article

Biodiesel, a renewable and environmentally friendly alternative to fossil fuels, has attracted significant attention due to its potential to reduce greenhouse gas emissions. However, high production costs and complex processing remain challenges. Heterogeneous catalysts have shown promise in overcoming these barriers by offering benefits, such as easy separation, reusability, low-cost raw materials, and the ability to reduce reaction times and energy consumption. This review evaluates key classes of heterogeneous catalysts, such as metal oxides, ion exchange resins, and zeolites, and their performance in transesterification and esterification processes. It highlights the importance of catalyst preparation methods, textural properties, including surface area, pore volume, and pore size, activation techniques, and critical operational parameters, like the methanol-to-oil ratio, temperature, time, catalyst loading, and reusability. The analysis reveals that catalysts supported on high surface area materials often achieve higher biodiesel yields, while metal oxides derived from natural sources provide cost-effective and sustainable options. Challenges, such as catalyst deactivation, sensitivity to feedstock composition, and variability in performance, are discussed. Overall, the findings underscore the potential of heterogeneous catalysts to enhance biodiesel production efficiency, although further optimization and standardized evaluation protocols are necessary for their broader industrial application. Full article

Land surface emissivity (LSE) is the most critical factor affecting land surface temperature (LST) retrieval. Understanding its variation characteristics is essential, as this knowledge provides fundamental prior constraints for the LST retrieval process. This study utilizes thermal infrared emissivity and hyperspectral data collected from diverse underlying surfaces from 2017 to 2024 to analyze LSE variation characteristics across different surface types, spectral bands, and temporal scales. Key influencing factors are quantified to establish empirical relationships between LSE dynamics and environmental variables. Furthermore, the impact of LSE models on diurnal LST retrieval accuracy is systematically evaluated through comparative experiments, emphasizing the necessity of integrating time-dependent LSE corrections into radiative transfer equations. The results indicate that LSE in the 8–11 µm band is highly sensitive to surface composition, with distinct dual-valley absorption features observed between 8 and 9.5 µm across different soil types, highlighting spectral variability. The 9.6 µm LSE exhibits strong sensitivity to crop growth dynamics, characterized by pronounced absorption valleys linked to vegetation biochemical properties. Beyond soil composition, LSE is significantly influenced by soil moisture, temperature, and vegetation coverage, emphasizing the need for multi-factor parameterization. LSE demonstrates typical diurnal variations, with an amplitude reaching an order of magnitude of 0.01, driven by thermal inertia and environmental interactions. A diurnal LSE retrieval model, integrating time-averaged LSE and diurnal perturbations, was developed based on underlying surface characteristics. This model reduced the root mean square error (RMSE) of LST retrieved from geostationary satellites from 6.02 °C to 2.97 °C, significantly enhancing retrieval accuracy. These findings deepen the understanding of LSE characteristics and provide a scientific basis for refining LST/LSE separation algorithms in thermal infrared remote sensing and for optimizing LSE parameterization schemes in land surface process models for climate and hydrological simulations. Full article

This paper presents a comparative study examining the effects of carbon nanotubes (CNTs) and expanded graphite (EG) on the thermal, mechanical, morphological, electrical, and piezoresistive properties of poly(ethylene-co-methacrylic acid) (EMAA) nanocomposites. To this end, different amounts of carbonaceous fillers (EG and CNTs separately) were added to the EMAA thermoplastic matrix, and the relative electrical percolation thresholds (EPTs) were determined. The effect of filler concentration on thermo-oxidative degradation and the EMAA crystallinity was investigated via thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), respectively. Dynamic mechanical analysis (DMA) demonstrated that both fillers enhance the Young’s and storage moduli, as well as the glass transition temperature, with a greater improvement for the bidimensional nanofiller, most likely due to the cumulative effect of more extensive EG-matrix interactions. In tensile tests, a very relevant difference was detected in the Gauge Factor (G.F.) and the elongation at break of the two typologies of nanocomposites. The G.F. of EMAA 10% CNT and EMAA 15% EG were found to be 0.5 ± 0.08 and 165 ± 14, respectively, while elongation at break was about 68% for EMAA 10% CNT and 8% for EMAA 15% EG. Emission Scanning Electron Microscopy (FESEM) and Tunneling Atomic Force Microscopy (TUNA) have contributed to explaining the differences between EG- and CNT-based nanocomposites from a morphological point of view, underlying the pivotal role of the filler aspect ratio and its structural features in determining different mechanical and piezoresistive performance. The comprehensive analysis of EMAA-EG and EMAA-CNT nanocomposites provides a guide for selecting the best self-sensing system for the specific application. More specifically, EMAA-CNT nanocomposites with high elongation at break and lower sensitivity to small strains are suitable for movement sensors in the soft robotic field, where high deformation has to be detected. On the other hand, the high sensitivity at a low strain of EMAA-EG systems makes them suitable for integrated sensors in more rigid composite structures, such as aeronautical and automotive components or wind turbines. Full article

High-entropy ceramics have gained wider attention due to their structural integrity and stability, which can be used in various functional applications. Especially, high-entropy oxides exhibit excellent thermal stability, particularly at high temperatures. Thermal barrier coating materials must demonstrate good thermal stability without any phase transformation or phase separation, which is critical in aerospace and energy conversion applications. To address this, we have prepared new high-entropy stannate pyrochlore oxide nanoparticles with the composition (Gd_0.2Nd_0.2La_0.2Pr_0.2Sm_0.2)₂Sn₂O₇ through a simple glycine-assisted sol–gel synthesis. The phase evolution was probed at different heat-treatment temperatures from 1000 °C to 1500 °C. Among the temperatures investigated, a single-phase pyrochlore oxide was formed from 1300 °C without any impurity or phase separation. The obtained nanoparticles were characterized using various techniques, including X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), nanoindentation, and dilatometry to investigate their physiochemical and mechanical properties. The Vickers hardness of high-entropy oxides is 4.2 ± 0.33 GPa, while a thermal expansion coefficient (TEC) of 8.7 × 10⁻⁶ K⁻¹ at 900 °C is calculated. The results show that the prepared high-entropy pyrochlore oxide can be a suitable candidate for thermal barrier coating. Full article

Developing resource-efficient technologies for producing ceramic materials with specific properties and performance characteristics is one of the most important tasks in modern materials science. As natural resources face depletion, the use of anthropogenic wastes, including fly ash from coal combustion, for the development of new compositions and the production of ceramics with an improved microstructure is of particular significance. The use of PM₁₀ fly ash microspheres in ceramic production will help to reduce particulate matter emissions. In this study, fine narrow fractions of PM₁₀ microspheres were successfully separated from coal fly ash using aerodynamic and magnetic separation. Glass–ceramic materials with a homogeneous microstructure, an open porosity of 0.4–37%, a compressive strength of 5–159 MPa, and acid resistance of up to 99.9% were obtained using narrow fractions. The materials obtained are promising for application as highly porous ceramics, effective microfiltration membranes, and fine-structured technical ceramics, which can be used in installations operating in aggressive media and/or at high temperatures. The ceramic membranes were characterised by high liquid permeability values up to 1194 L·m⁻²·h⁻¹·bar⁻¹. Filtration tests showed that the retention coefficient for dispersed microsilica particles with d_av = 1.9 μm is 0.99. Full article

The chemical industry faces major challenges worldwide. Since 1950, production has increased 50-fold and is projected to continue growing, particularly in Asia. It is one of the most energy- and resource-intensive industries, contributing significantly to greenhouse gas emissions and the depletion of finite resources. This development exceeds planetary boundaries and calls for a sustainable transformation of the industry. The key transformation areas are as follows: (1) Non-Fossil Energy Supply: The industry must transition away from fossil fuels. Renewable electricity can replace natural gas, while green hydrogen can be used for high-temperature processes. (2) Circularity: Chemical production remains largely linear, with most products ending up as waste. Sustainable product design and improved recycling processes are crucial. (3) Non-Fossil Feedstock: To achieve greenhouse gas neutrality, oil, gas, and coal must be replaced by recycling plastics, renewable biomaterials, or CO₂-based processes. (4) Sustainable Chemical Production: Energy and resource savings can be achieved through advancements like catalysis, biotechnology, microreactors, and new separation techniques. (5) Sustainable Chemical Products: Chemicals should be designed to be “Safe and Sustainable by Design” (SSbD), meaning they should not have hazardous properties unless essential to their function. (6) Sufficiency: Beyond efficiency and circularity, reducing overall material flows is essential to stay within planetary boundaries. This shift requires political, economic, and societal efforts. Achieving greenhouse gas neutrality in Europe by 2050 demands swift and decisive action from industry, governments, and society. The speed of transformation is currently too slow to reach this goal. Science can drive innovation, but international agreements are necessary to establish a binding framework for action. Full article

One of the most promising methods for direct carbon dioxide (CO₂) capture from the atmosphere is using material-based adsorption. Fly ash, a solid waste material, has been found to have good adsorption potential for CO₂. Since different fly ashes have different properties, their CO₂ adsorption behaviors differ; therefore, it is important to develop separate isotherms for each fly ash to quantify its CO₂ adsorption capacity. This research investigates the adsorption capacity of an extremely abundant volcanic fly ash in Egypt that is currently being researched for use in CO₂ capture applications in Egypt. Adsorption was measured using the volumetric adsorption principle. Four adsorption isotherms for the volcanic fly ash were developed at different temperatures, including 23, 40, 60, and 80 °C. The adsorption capacity was found to be impacted by the temperature of the experiment, the pressure of the CO₂, and the interactions occurring between the CO₂ and the fly ash. As the temperature increased, the adsorption capacity increased significantly. This was primarily due to the expansion of fly ash particles at elevated temperatures, which resulted in a higher contact surface area between the fly ash and the CO₂. This created more adsorption sites for the CO₂, therefore increasing the CO₂ adsorption potential significantly. This research can help facilitate the use of volcanic fly ash for CO₂ capture applications in Egypt in the near future, hence reducing the overall CO₂ emissions to the atmosphere. Full article