Search Results (186)

Enhanced Geothermal Systems (EGS) require thermochemically stable proppant materials capable of sustaining fracture conductivity under harsh subsurface conditions. This study systematically investigates the response of commercial proppants to coupled thermo-hydro-chemical (THC) effects, focusing on chemical stability and microstructural evolution. Four proppant types were evaluated: an ultra-low-density ceramic (ULD), a resin-coated sand (RCS), and two quartz-based silica sands. Experiments were conducted under simulated EGS conditions at 130 °C with daily thermal cycling over a 25-day period, using diluted site-specific Utah FORGE geothermal fluids. Static batch reactions were followed by comprehensive multi-modal characterization, including scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS), X-ray diffraction (XRD), and micro-computed tomography (micro-CT). Proppants were tested in both granular and powdered forms to evaluate surface area effects and potential long-term reactivity. Results indicate that ULD proppants experienced notable resin degradation and secondary mineral precipitation within internal pore networks, evidenced by a 30.4% reduction in intragranular porosity (from CT analysis) and diminished amorphous peaks in the XRD spectra. RCS proppants exhibited a significant loss of surface carbon content from 72.98% to 53.05%, consistent with resin breakdown observed via SEM imaging. While the quartz-based sand proppants remained morphologically intact at the macro-scale, SEM-EDS revealed localized surface alteration and mineral precipitation. The brown sand proppant, in particular, showed the most extensive surface precipitation, with a 15.2% increase in newly detected mineral phases. These findings advance understanding of proppant–fluid interactions under low-temperature EGS conditions and underscore the importance of selecting proppants based on thermo-chemical compatibility. The results also highlight the need for continued development of chemically resilient proppant formulations tailored for long-term geothermal applications. Full article

High ash content in algal biomass limits its suitability for biofuel production by reducing combustion efficiency and increasing fouling. This study presents a green deashing strategy using nitrilotriacetic acid (NTA) and deionized (DI) water to purify Scenedesmus algae, which was selected for its high ash removal potential. The optimized sequential treatment (DI, NTA chelation, and DI+NTA treatment at 90–130 °C) achieved up to 83.07% ash removal, reducing ash content from 15.2% to 3.8%. Elevated temperatures enhanced the removal of calcium, magnesium, and potassium, while heavy metals like lead and copper were reduced below detection limits. CHN analysis confirmed minimal loss of organic content, preserving biochemical integrity. Unlike traditional acid leaching, this method is eco-friendly after three cycles. The approach offers a scalable, sustainable solution to improve algal biomass quality for thermochemical conversion and supports circular bioeconomy goals. Full article

Chile is among the leading global exporters of pulp and paper, supported by extensive plantations of Pinus radiata and Eucalyptus spp. This review synthesizes recent progress in the valorization of forestry biomass in Chile, including both established practices and emerging bio-based applications. It highlights advances in lignin utilization, nanocellulose production, hemicellulose processing, and tannin extraction, as well as developments in thermochemical conversion technologies, including torrefaction, pyrolysis, and gasification. Special attention is given to non-timber forest products and essential oils due to their potential bioactivity. Sustainability perspectives, including Life Cycle Assessments, national policy instruments such as the Circular Economy Roadmap and Extended Producer Responsibility (REP) Law, are integrated to provide context. Barriers to technology transfer and industrial implementation are also discussed. This work contributes to understanding how forestry biomass can support Chile’s transition toward a circular bioeconomy. Full article

Solar fuels production requires developing redox active materials with porous structures able to withstand thermochemical cycles with enhanced thermal stability under concentrated solar irradiation conditions. The mechanical performance of 3D-printed, macroporous black zirconia gyroid structures, coated with redox-active ceria, was assessed for their suitability in solar thermochemical cycles for CO₂ and H₂O splitting. Experiments were conducted using a 1.5 kW solar furnace to supply the high-temperature concentrated heat to a windowed reaction chamber to carry out thermal redox cycling under realistic on-sun conditions. The ceria coating on ceramic structures improved the thermal stability and redox efficiency while minimizing the quantity of the redox material involved. Crushing strength measurements showed that samples not directly exposed to the concentrated solar flux retained their mechanical performance after thermal cycling (~10 MPa), while those near the concentrated solar beam focus exhibited significant degradation due to thermal stresses and the formation of Ce_xZr_1−xO₂ solid solutions (~1.5 MPa). A Weibull modulus of 8.5 was estimated, marking the first report of such a parameter for fused filament fabrication (FFF)-manufactured black zirconia with gyroid architecture. Failure occurred via a damage accumulation mechanism at both micro- and macro-scales. These findings support the viability of ceria-coated cellular ceramics for scalable solar fuel production and highlight the need for optimized reactor designs. Full article

In this study, sugarcane bagasse (SCB), an abundant agricultural byproduct, was transformed into activated carbon via a controlled thermochemical pyrolysis route for high-performance energy storage applications. Herein, we utilized the activated carbon derived from pure sugarcane bagasse (SCB-AC) and further activated using KOH (SCB-KOH-AC) as an electrode material in aqueous symmetric supercapacitor configurations. The synthesized activated carbon was subjected to analysis using a range of characteristics including FT-Raman spectroscopy, which was employed to confirm the functional groups present in the carbon materials. The XPS analysis provided insights into the elemental composition and ionic states. The SEM analysis revealed that both activated carbon and KOH/activated carbon materials exhibited a layered or stacked, albeit slightly random, orientation. Electrochemical studies demonstrated that the synthesized carbon electrodes exhibited impressive specific capacitance values of (SCB) activated carbon (132.20 F/g) and KOH-activated, pure SCB AC (SCB-A) 253.41 F/g at 0.5 A/g. Furthermore, the SCB KOH-activated carbon (AC) electrode revealed a higher specific capacitance value and A//SCB-A symmetric devices delivered energy density reaching 17.91 Wh/kg and power density up to 2990 W/kg. The KOH-activated carbon electrode demonstrated remarkable cycling stability retaining 93.89%, even after 10,000 cycles. These results suggest that the sugarcane bagasse-derived activated carbon is a sustainable and low-cost candidate for next-generation supercapacitor electrodes. The results demonstrate enhanced capacitance, stability, and pore structure tailored for energy storage applications. The KOH-activated carbon SCB carbon symmetric device with symmetric electrodes exhibited a suitable bio-mass carbon for future energy storage applications. Full article

This study provides a comprehensive review of molten salt technology, as well as electrochemical and thermochemical processes aimed at hydrogen and syngas production. First, this research illustrates the current types of molten salt mixtures, detailing their main applications and thermophysical properties. Then, the analysis delves into existing thermo-electrochemical cycles and their specific operating conditions for producing hydrogen and syngas. Moreover, this study assesses the compatibility of these processes with molten salt integration. This investigation involved a comprehensive review of the existing technical and scientific literature, blending insights and practical experiences to offer detailed data on the topics explored. The findings suggest that molten salts, with their medium–high operating temperatures, can markedly improve the efficiency and sustainability of hydrogen and syngas production. Furthermore, this study outlines the pivotal role these technologies can play in achieving the European Union’s ambitious goals by enhancing the use of renewable energy sources and advancing the shift to carbon-free solutions. Full article

This study provides a comprehensive thermochemical characterization of common nut residues—almonds, walnuts, hazelnuts, peanuts, and pistachios shells—as potential biomass fuels, examining their chemical composition, calorific values, and emissions profiles. Their suitability as renewable energy sources was systematically assessed by verifying compliance with ISO 17225-2 standards for pellet production. The nut residues demonstrated promising energy characteristics, with higher heating values ranging from 17.75 to 19.12 MJ/kg and most samples fulfilling ISO 17225-2 classifications A1 or A2. Specifically, the walnut residues met the highest quality classification (A1), whereas the almond, hazelnut, and pistachio residues met the A2 classification, and the peanut residues were classified as B due to higher nitrogen content. A Life Cycle Assessment (LCA) was also performed to quantify the environmental impacts, focusing on CO₂ emissions from energy recovery and transportation. The results showed significantly lower CO₂ emissions from all the nut residues compared to fossil fuels such as coal, natural gas, fuel oil (HFO), and LPG. The almond residues exhibited the lowest total CO₂ emissions at 1669.27 kg CO₂ per ton, while the peanuts had the highest at 1945.93 kg CO₂ per ton. Even the highest-emitting nut residues produced substantially lower emissions compared to coal, which emitted approximately 4581.12 kg CO₂ per ton. These findings highlight the potential of nut residues as low-carbon, renewable energy sources, providing both environmental advantages and opportunities to support local agricultural economies. Full article

Fuel cell electric vehicles (FCEVs) offer a promising solution for energy saving and emission reduction in transportation. However, several challenges must be addressed for their application. This study conducts a full life cycle assessment (LCA) of FCEVs, dividing it into the fuel cycle and vehicle cycle to separately assess energy consumption (EC) and emissions. The fuel cycle examined 18 hydrogen production–storage–transport pathways, while the vehicle cycle evaluates energy use and emissions associated with vehicle component production, assembly, disposal, battery production, and fluid consumption. Based on the GREET database, total energy consumption and emissions over a lifetime were calculated. Five environmental impact indicators were used for evaluation, and a comprehensive environmental assessment (CEA) indicator was established for different scenarios. Results indicate that nuclear thermochemical water splitting is the best hydrogen production method, and pipeline transportation is the most efficient for hydrogen transport. Additionally, water electrolysis for hydrogen production is only practical when paired with renewable energy. The study also identified that the Hydrogen production method, “Body”, “Proton Exchange Membrane Fuel Cells (PEMFCs) System”, “Chassis”, “Hydrogen Storage System” and lifetime significantly impact energy consumption and emissions. These stages or products represent high-impact leverage points for enhancing the lifecycle sustainability evaluation of FCEVs. Full article

Nuclear energy cogeneration, which integrates electricity generation with thermal energy utilization, presents a transformative pathway for enhancing energy efficiency and decarbonizing industrial and urban sectors. This comprehensive review synthesizes advancements in technological stratification, economic modeling, and sectoral practices to evaluate the viability of nuclear cogeneration as a cornerstone of low-carbon energy transitions. By categorizing applications based on temperature requirements (low: <250 °C, medium: 250–550 °C, high: >550 °C), the study highlights the adaptability of reactor technologies, including light water reactors (LWRs), high-temperature gas-cooled reactors (HTGRs), and molten salt reactors (MSRs), to sector-specific demands. Key findings reveal that nuclear cogeneration systems achieve thermal efficiencies exceeding 80% in low-temperature applications and reduce CO₂ emissions by 1.5–2.5 million tons annually per reactor by displacing fossil fuel-based heat sources. Economic analyses emphasize the critical role of cost allocation methodologies, with exergy-based approaches reducing levelized costs by 18% in high-temperature applications. Policy instruments, such as carbon pricing, value-added tax (VAT) exemptions, and subsidized loans, enhance project viability, elevating net present values by 25–40% for district heating systems. Case studies from Finland, China, and Canada demonstrate operational successes, including 30% emission reductions in oil sands processing and hydrogen production costs as low as USD 3–5/kg via thermochemical cycles. Hybrid nuclear–renewable systems further stabilize energy supply, reducing the levelized cost of heat by 18%. The review underscores the necessity of integrating Generation IV reactors, thermal storage, and policy alignment to unlock nuclear cogeneration’s full potential in achieving global decarbonization and energy security goals. Full article

This review paper presents an overview of fuel cell electrochemical systems that can be used for clean large-scale power generation and energy storage as global energy concerns regarding emissions and greenhouse gases escalate. The fundamental thermochemical and operational principles of fuel cell power generation and electrolyzer technologies are discussed with a focus on high-temperature solid oxide fuel cells (SOFCs) and solid oxide electrolysis cells (SOECs) that are best suited for grid scale energy generation. SOFCs and SOECs share similar promising characteristics and have the potential to revolutionize energy conversion and storage due to improved energy efficiency and reduced carbon emissions. Electrochemical and thermodynamic foundations are presented while exploring energy conversion mechanisms, electric parameters, and efficiency in comparison with conventional power generation systems. Methods of converting hydrocarbon fuels to chemicals that can serve as fuel cell fuels are also presented. Key fuel cell challenges are also discussed, including degradation, thermal cycling, and long-term stability. The latest advancements, including in materials selection research, design, and manufacturing methods, are also presented, as they are essential for unlocking the full potential of these technologies and achieving a sustainable, near zero-emission energy future. Full article

This paper reports the latest update to and a 24 h continuous operation test of the CEU’s thermochemical iodine–sulfur cycle water-splitting system with a maximum H₂ hydrogen production capacity of 1500 L/h. To address challenges such as high energy consumption and severe corrosion in traditional processes, the system was updated and optimized by introducing a small-cycle design, simulated using Aspen Plus software, achieving a thermal efficiency of 53%. Specifically, the key equipment improvements included a three-stage H₂SO₄ decomposition reactor and an HI decomposition reactor with heat recovery, resolving issues of severe corrosion when H₂SO₄ boils and reducing heat loss. During 24 h continuous operation in January 2025, the system achieved a peak hydrogen production rate of 1536 L/h and a long-term stable rate of approximately 300 L/h, with hydrogen purity reaching up to 98.75%. This study validates the potential for the scaling up of iodine–sulfur cycle hydrogen production technology, providing engineering insights for efficient and clean hydrogen energy production. Full article

Hydrogen and some of its derivatives (such as e-methanol, e-methane, and e-ammonia) are promising energy carriers that have the potential to replace conventional fuels, thereby eliminating their harmful environmental impacts. An innovative use of hydrogen as a zero-emission fuel is forming weakly ionized plasma by seeding the combustion products of hydrogen with a small amount of an alkali metal vapor (cesium or potassium). This formed plasma can be used as a working fluid in supersonic open-cycle magnetohydrodynamic (OCMHD) power generators. In these OCMHD generators, direct-current (DC) electricity is generated straightforwardly without rotary turbogenerators. In the current study, we quantitatively and qualitatively explore the levels of electric conductivity and the resultant volumetric electric output power density in a typical OCMHD supersonic channel, where thermal equilibrium plasma is accelerated at a Mach number of two (Mach 2) while being subject to a strong applied magnetic field (applied magnetic-field flux density) of five teslas (5 T), and a temperature of 2300 K (2026.85 °C). We varied the total pressure of the pre-ionization seeded gas mixture between 1/16 atm and 16 atm. We also varied the seed level between 0.0625% and 16% (pre-ionization mole fraction). We also varied the seed type between cesium and potassium. We also varied the oxidizer type between air (oxygen–nitrogen mixture, 21–79% by mole) and pure oxygen. Our results suggest that the ideal power density can reach exceptional levels beyond 1000 MW/m³ (or 1 kW/cm³) provided that the total absolute pressure can be reduced to about 0.1 atm only and cesium is used for seeding rather than potassium. Under atmospheric air–hydrogen combustion (1 atm total absolute pressure) and 1% mole fraction of seed alkali metal vapor, the theoretical volumetric power density is 410.828 MW/m³ in the case of cesium and 104.486 MW/m³ in the case of potassium. The power density can be enhanced using any of the following techniques: (1) reducing the total pressure, (2) using cesium instead of potassium for seeding, and (3) using air instead of oxygen as an oxidizer (if the temperature is unchanged). A seed level between 1% and 4% (pre-ionization mole fraction) is recommended. Much lower or much higher seed levels may harm the OCMHD performance. The seed level that maximizes the electric power is not necessarily the same seed level that maximizes the electric conductivity, and this is due to additional thermochemical changes caused by the additive seed. For example, in the case of potassium seeding and air combustion, the electric conductivity is maximized with about 6% seed mole fraction, while the output power is maximized at a lower potassium level of about 5%. We also present a comprehensive set of computed thermochemical properties of the seeded combustion gases, such as the molecular weight and the speed of sound. Full article

This study presents a methodology for assessing the technical and economic potential of electricity generation from biomass residues, using thermochemical conversion technologies. Applied in the state of Minas Gerais, Brazil, the analysis focuses on residues from corn, soybean, coffee, eucalyptus, and sugarcane. A multi-criteria decision-making (MCDM) approach, integrated with GIS, was used to identify the most viable biomass sources and most suitable conversion technologies, namely the Rankine cycle, organic Rankine cycle, and gasification with internal combustion engines, based on Technological Readiness Levels (TRLs). Eucalyptus emerged as the most suitable residue due to its high energy density, while sugarcane residues were the most abundant. The economic feasibility analysis indicates levelized costs ranging from USD 0.10 to USD 0.24 per kWh, with the conventional Rankine cycle emerging as the most cost-effective option for plants with a capacity exceeding 5 MWe. The proposed methodology supports strategic bioenergy planning by integrating geospatial, technological, and economic factors. Full article

Superdeep diamonds and their syngenetic inclusions are crucial for understanding Earth’s deep carbon cycle and slab–mantle redox dynamics. The origins of these diamonds, especially their links to iron (Fe) carbides and ferropericlase with varying Mg# [=Mg/(Mg+Fe)_at], however, remain elusive. In this study, we performed high pressure–temperature (P-T) experiments (10–16 GPa and 1200–1700 K) across cold-to-warm subduction zones using a multi-anvil press. The results reveal a stepwise Fe-mediated carbonate reduction process for the formation of superdeep diamonds: MgCO₃ → Fe-carbides (Fe₃C/Fe₇C₃) → graphite/diamond. This mechanism explains two phenomena regarding superdeep diamonds: (1) anomalous ¹³C depletion results from kinetic isotope fractionation during ¹²C enrichment into the intermediate Fe-carbides; (2) nitrogen scarcity is due to Fe-carbides acting as nitrogen sinks. Ferropericlase [(Mg,Fe)O] formed during the reactions in our experiments shows Mg# variations (0.2–0.9), similar to those found in natural samples. High Mg# (>0.7) variants from lower temperature experiments indicate diamond crystallization from carbonatitic melts in the shallow lower mantle, while the broad Mg# range (0.2–0.9) from experiments at higher temperatures suggests multi-depth formation processes as found in Brazilian diamonds. These findings suggest that slab–mantle interactions produce superdeep diamonds with distinctive Fe-carbides and ferropericlase assemblages as inclusions, coupled with their ¹³C- and nitrogen-depleted signatures, which underscore thermochemical carbon cycling as a key factor in deep carbon storage and mantle mineralogy. Full article

The increasing global demand for clean water is driving the development of advanced wastewater treatment technologies. Graphitic carbon nitride (g-C₃N₄) has emerged as an efficient photocatalyst for degrading organic pollutants, such as synthetic dyes, due to its exceptional thermo-chemical stability. However, its application is limited by an insufficient specific surface area, low photocatalytic efficiency, and an unclear degradation mechanism. In this study, we aimed to enhance g-C₃N₄ by doping it with elemental chlorine, resulting in a series of Cl-C₃N₄ photocatalysts with varying doping ratios, prepared via thermal polymerization. The photocatalytic activity of g-C₃N₄ was assessed by measuring the degradation rate of RhB. A comprehensive characterization of the Cl-C₃N₄ composites was conducted using SEM, XRD, XPS, PL, DRS, BET, EPR, and electrochemical measurements. Our results indicated that the optimized 1:2 Cl-C₃N₄ photocatalyst exhibited exceptional performance, achieving 99.93% RhB removal within 80 min of irradiation. TOC mineralization reached 91.73% after 150 min, and 88.12% removal of antibiotics was maintained after four cycles, demonstrating the excellent stability of the 1:2 Cl-C₃N₄ photocatalyst. Mechanistic investigations revealed that superoxide radicals (·O₂⁻) and singlet oxygen (¹O₂) were the primary reactive oxygen species responsible for the degradation of RhB in the chlorine-doped g-C₃N₄ photocatalytic system. Full article