Search Results (3,932)

The Amazonian açaí waste is promising for producing charcoal through pyrolysis and bioenergy through combustion, but the property losses from its poor disposal in the environment remain unknown. Therefore, this work aimed to analyze how different storage conditions of the açaí waste over time, which mimic the reality throughout the Amazon, modify its bioenergetic properties. The samples were stored in a covered greenhouse for nine months in the following conditions: immersed in water, on the soil, and in open plastic bags. The biomass was analyzed by Fourier-transformed near-infrared spectroscopy, physical properties, stereomicroscopy, proximate composition, and thermogravimetry. The degraded waste showed endocarp attack and fungi proliferation. The chemical groups of primary cell wall components were concentrated, unlike water-soluble materials, raising the fixed carbon from 22% to 25% after 30 days. Consequently, higher heating values were kept (≈19 MJ/kg). However, water immersion storage sharply decreased the waste basic density from 0.81 g/cm³ to 0.56 g/cm³, dropping the energy density from 12 GJ/m³ to 8 GJ/m³. Moreover, storage raised ash content from 1.1% up to 1.9%. The storage hindered the start of the main phases of combustion and pyrolysis, which were later intensified, especially for soil-stored waste. Therefore, more stable combustion and pyrolysis require fresh waste. Besides natural drying, plastic bag storage over time kept the waste quality closer to that of the fresh waste. Full article

This study investigates the development of a composite material based on agricultural plant waste from Kazakhstan, utilizing a multicomponent binder incorporated with rice husk ash. The implementation of low-clinker binders enables the full utilization of ash dumps from the Kyzylorda thermal power plant (TPP) and rice husk residues from local rice-processing enterprises. Physical and chemical analysis of the ash–cement stone revealed a reduction in portlandite content compared to control samples. Phase composition analysis indicated the presence of hydroaluminate C₄AH₁₃ and a reduction in calcite, suggesting accelerated crystallization of calcium silicate hydrates. The formation of crystalline phases and intergrowth structures is assumed to contribute to the strengthening of the gel-like matrix. Experimental optimization of the ash–cement binder with rice husk ash yielded compressive strengths ranging from 3.03 to 4.10 MPa at densities of 790–900 kg/m³, depending on the type of organic filler. These results confirm the feasibility of using locally sourced agricultural waste for the production of heat-insulating and structurally stable composite materials. Full article

The improper disposal of end-of-life tires poses significant environmental challenges due to their petroleum-based composition and slow degradation, while simultaneously representing an underutilized energy resource. This study investigates the slow pyrolysis of shredded waste tires in a fixed-bed electrically heated reactor to evaluate the production and fuel properties of gaseous, liquid, and solid fractions. Experiments were conducted with 100 g samples under nitrogen at final temperatures of 400, 500, and 600 °C, with residence times of 40, 25, and 10 min, respectively. Higher temperatures promoted gas formation, increasing yields from 27% to 32% and achieving a maximum lower heating value of 30.54 MJ m⁻³ at 600 °C, with enhanced H₂ and CH₄ contents. Solid yields decreased slightly (41% to 37%), while char maintained stable heating values (~29 MJ kg⁻¹). Liquid yields remained near 33% and showed high calorific values (~41 MJ kg⁻¹), densities of 700–770 kg m⁻³, low acidity, low ash content, and increased viscosity at higher temperatures. Energy conversion efficiency reached 74.4% at 500 °C. The integrated evaluation of all fractions under identical conditions highlights fixed-bed pyrolysis as a promising pathway for waste-tire valorization and decentralized fuel production. Full article

Anaerobic digesters operating under neotropical conditions face significant technological constraints. High humidity, intense solar radiation, and pronounced diurnal temperature variations increase conductive, convective, and radiative heat losses. These factors reduce internal thermal stability and directly affect methane production rates and overall energy efficiency. As a result, thermal instability becomes a recurrent operational bottleneck in biogas plants without active temperature control. This review examines the thermal and dynamic behavior of anaerobic reactors from a process-engineering perspective. It integrates energy balances, heat-transfer mechanisms, and computational fluid dynamics (CFD) modeling. The combined effects of temperature gradients, hydrodynamic mixing patterns, and structural material properties are analyzed to determine their influence on thermal homogeneity, microbial stability, and methane yield consistency under mesophilic conditions. Technological strategies to mitigate thermal losses are evaluated. These include passive insulation using low-conductivity materials, geometry optimization supported by numerical modeling, and thermal recirculation schemes, as these factors govern temperature distribution and process resilience. Current limitations are also discussed, particularly the frequent decoupling between ADM1-based kinetic models and transient heat-transfer analysis. This separation restricts predictive capability under real-scale diurnal temperature oscillations. The development and validation of coupled hydrodynamic–thermal–biokinetic models under fluctuating neotropical boundary conditions are proposed as critical steps. Such integrated approaches can enhance operational stability, ensure consistent methane production, and improve energy self-sufficiency in organic waste valorization systems. Full article

Indoor swimming pools require ventilation and precise temperature and humidity control, leading to significant energy consumption. This study investigated the use of liquid desiccant technology to reduce energy consumption for heating and dehumidification of two indoor swimming pools in a UK leisure centre. Through dynamic modelling and techno-economic analysis, this research quantified heat losses in the pools, simulated the performance of liquid desiccant technology, evaluated the economic benefits and cost implications of regenerating the desiccant solution using waste heat, and assessed the feasibility of adopting the technology across the entire UK. The results showed that evaporative losses were the dominant heat loss mechanism for both pools, while the proposed liquid desiccant system effectively maintained optimal temperature and humidity conditions. Additionally, pool water can serve as a heat sink after desiccant regeneration, thereby reducing the energy demand for pool water heating. Energy consumption could be reduced by 68.9–76.7% when using a cooling tower and 77.5–88.1% when using pool water for heat rejection, with internal rates of return that can exceed 15% for the most cost-effective configurations. If the regeneration heat is sourced externally, up to £34.7/MWh could be paid for the heat required while ensuring the cost-effectiveness of the process. These findings suggest that liquid desiccant systems can reduce heating and dehumidification energy in indoor swimming pools when low-temperature heat is available for regeneration. Future research should focus on experimental validation, addressing interactions with chlorine gases, long-term system performance and real-world implementation challenges to ensure commercial deployment. Full article

To investigate the influence of working fluid composition on the thermo-hydraulic performance of plate heat exchangers (PHEs) under single-phase sensible heat transfer conditions, a three-dimensional steady-state numerical model was developed for a transverse corrugated channel with a chevron angle of 60°. The governing equations were solved using the finite volume method implemented in ANSYS Fluent, in conjunction with the standard k–ε turbulence model. The analysis considered pure refrigerants R134a and R245fa, as well as their mixtures with mass ratios of 0.2, 0.5, and 0.8, with thermophysical properties assumed to be temperature-independent constants. The results indicate that as the mass fraction of R134a decreases from 1.0 to 0, the heat transfer coefficient (h) decreases from 1025 to 815 W/(m²·K), primarily attributed to the combined effects of reduced thermal conductivity and increased viscosity. Among the investigated cases, the R134a/R245fa mixture with a mass ratio of 0.8 provides the most favorable performance trade-off, exhibiting a heat transfer coefficient only 3.0% lower than that of pure R134a while achieving a 12.5% reduction in flow resistance compared with pure R245fa. Furthermore, the heat transfer coefficient is found to be weakly affected by heat flux in the range of 8000–20,000 W/m²; in contrast, increasing the mass flow rate from 0.001 to 0.005 kg/s enhances heat transfer coefficient by 65.1%, accompanied by a significant increase in pressure drop. Comparisons with established single-phase correlations for corrugated channels show average deviations of 6.5% for the Nusselt number and 3.8% for the friction factor. The present study provides useful guidance for working fluid selection and operational optimization of PHEs in applications dominated by sensible heat transfer, such as specific stages of heat pump cycles and medium-temperature waste heat recovery. Full article

Food waste is commonly valorized through aerobic composting, yet the responses of water-soluble organic carbon (WSOC) across molecular-weight (MW) fractions remain insufficiently resolved. This study aimed to quantify how distinct composting strategies regulate WSOC MW distribution and compositional evolution and identify the key physicochemical drivers. Food waste was treated by 30-day conventional composting (CK), 15-day phased inoculation (JJ; 2% (w/w) antioxidative consortium dominated by Bacillus/Pseudomonas followed by 2% (w/w) thermophilic cellulolytic consortium enriched in Geobacillus/Paenibacillus when the temperature reached 50 °C), and 24-h rapid thermophilic composting (RC; 2% (w/w) inoculation with a 24-h moist-heat pretreatment). RC yielded a small molecular weight organic carbon (SMOC)-rich product with low aromaticity, with MW < 5 kDa accounting for 68.21% (MW < 500 Da: 28.50%). JJ preferentially enriched more oxidized, fulvic-like/carboxyl-rich organics, increasing the fulvic-like contribution from 15.97% to 35.40% and raising the HMOC/SMOC to 2.72:1. CK showed the strongest humification, with MW > 5 kDa reaching 65.56% and humic-like Region V increasing from 26.25% to 66.36%. pH was the primary predictor of MW (day 6: CK 3.9; JJ 4.9; final ~8.8), while temperature jointly governed humic-like formation in RC. Full article

Several hydrogen explosions have been reported in ash treatment facilities at municipal solid waste incineration plants, highlighting the need for effective suppression measures. This study focuses on controlling temperature changes during the conveyor transportation process as a method to reduce hydrogen generation from incineration ash. Experiments were conducted in which heated simulated incineration ash was immersed in water inside a vessel and allowed to cool naturally. The results show that higher water temperatures during immersion significantly decreased the amount of hydrogen gas generated. Specifically, it was found that hydrogen generation ceased when the simulated incineration ash was immersed in water at 90 °C and subsequently allowed to cool naturally. These findings suggest that temperature control may contribute to preventing hydrogen explosion hazards in ash handling systems. Full article

Within a waste biorefinery framework, integrating agro-industrial by-products into the circular economy requires a detailed understanding of the thermochemical conversion behaviour of low-grade carbonaceous materials. This study evaluates the co-pyrolysis characteristics of Soma lignite (SL) and pectin-rich sugar beet pulp (SBP) as a sustainable route for upgrading these resources into clean energy carriers. Interactions between the two feedstocks were analysed by thermogravimetric measurements, triple-region kinetic modelling, and quantitative synergy indices at six mixing ratios, including the pure samples (100:0, 80:20, 60:40, 40:60, 20:80, and 0:100 wt% SL:SBP). The Reactivity Index ($R_{\mathrm{m}}$) increased from 0.97 × 10⁻⁴ s⁻¹K⁻¹ for pure SL to 8.65 × 10⁻⁴ s⁻¹K⁻¹ for the 20:80 blend, showing that SBP acts as a highly reactive biomass component that accelerates devolatilisation in the main pyrolysis region. Synergy analysis indicated a shift from inhibitory behaviour in coal-rich blends to slightly positive synergy in SBP-rich mixtures, with the onset of positive $\Delta TC$ around 60 wt% SBP under the present single-heating-rate, non-replicated TGA conditions. This tentative threshold-like behaviour suggests that a critical level of literature-supported, hypothesised hydrogen-donating biomass radicals may be required to overcome the structural resistance of the coal matrix. Within these experimental limitations, the apparent macro-kinetic deviations and first-order Arrhenius parameters suggest that SL/SBP co-pyrolysis follows a complex, non-additive pathway that should be further validated by multi-heating-rate and product characterisation studies in future work. The primary contribution of this work lies in proposing this distinct threshold-like biomass fraction at the macro-kinetic level that governs the transition from heat-transfer-limited antagonism to radical-influenced synergy in low-rank coal and pectin-rich biomass blends. Overall, the combined $\Delta TC$, $\Delta E$ and $R_{\mathrm{m}}$ descriptors provide useful macro-kinetic benchmarks for guiding the optimisation of thermochemical processes for low-grade carbonaceous resources. Full article

Direct air capture (DAC) of CO₂ via temperature-swing adsorption (TSA) can support sustainable carbon dioxide removal, but only if sorbents regenerate with low energy demand and maintain performance under humid ambient air. In this paper, we evaluate three commercial molecular sieves (JLPM3, 13X, and 4A) in packed-bed tests using humid ambient air. We compared 40 g samples as received with 200 g samples conditioned for 12 days at 100 °C to emulate prolonged exposure to regeneration temperature (the cumulative effect of many heating/desorption cycles); all cycle-stabilized uptake values are reported from the conditioned materials. JLPM3 delivered the highest stabilized CO₂ uptake (0.24 ± 0.01 mmol·g⁻¹), consistent with a combined physisorption/chemisorption mechanism. Its higher total porosity (26.190%) and smaller mesopores (7.569 nm width) promoted rapid mass transfer and site accessibility, while slightly greater micropore area (710.285 m²·g⁻¹) and volume (0.267 cm³·g⁻¹) than 13X supported its marginally higher capacity. Evidence of partial structural degradation under mechanical and thermal stress indicates that minimizing strain during cycling will be important for scale-up and for reducing sorbent replacement. Conditioning at 100 °C activated additional chemisorption sites across all sieves but reduced physisorption capacity. Importantly, a ~100 °C desorption step fully regenerated physisorbed CO₂ while purging moisture from zeolite pores, indicating that low-temperature TSA (compatible with low-grade or waste heat) can replace harsher 300 °C regeneration and lower energy demand. CO₂–H₂O competition experiments confirmed substantial site occupancy by water vapor, which limits capture under humid conditions and motivates water management strategies. Overall, maximizing DAC performance requires tailoring pore structure and operating conditions while preserving sorbent integrity; JLPM3 emerges as a promising candidate for more energy- and resource-efficient DAC. Full article

Binary-cycle geothermal plants are inherently limited by thermodynamics, forcing operators to reinject fluids at temperatures that are still valuable for direct heating. This process results in substantial exergetic waste. While prior research has examined efficiency at the level of individual plants, this study introduces a regional-scale framework to convert these facilities into multi-purpose energy hubs. The research focuses on Türkiye’s Western Anatolia Graben, a region with high geothermal activity that, paradoxically, remains dependent on fossil fuels. By combining meteorological records with operational plant data, we evaluated the existing housing stock of 983,277 residences across 14 districts and modeled the heating requirements for a targeted capacity of 468,719 residences that the proposed system can serve. The results indicate that the currently wasted thermal load in 10 specific districts, including key centers such as Sarayköy and Alaşehir, is sufficient to cover peak winter heating demands without fossil fuel backup. Although the infrastructure requires a significant initial investment of $4.51 billion, the project demonstrates long-term viability with a Levelized Cost of Heat (LCOH) of 62.94 USD/MWh and a payback period of 10.43 years. Beyond economic considerations, the system serves as a major decarbonization tool, capable of cutting residential CO₂ emissions by 1.7 million tons annually (a 47.7% reduction). These findings suggest that policy incentives should move away from electricity-only models toward integrated reservoir management to maximize resource efficiency. Full article

Carbon dioxide (CO₂) capture is a cornerstone of global carbon neutrality, yet the high energy penalty associated with solvent regeneration—particularly for monoethanolamine (MEA) systems—remains a major barrier to its sustainable deployment. This study presents a sustainable and high-performance catalytic solution using micro-sized iron oxyhydroxide (β-FeOOH). Characterized by a high specific surface area ($287 m²/g) and a synergistic distribution of abundant Lewis and Brønsted acid sites, the β-FeOOH catalyst significantly enhances CO₂ desorption kinetics. Experimental results demonstrate that the incorporation of β-FeOOH into a 30 wt% MEA solution increases the CO₂ desorption rate by 10.9% while simultaneously lowering the regeneration temperature from the conventional 120 °C to 85 °C. Such a reduction in thermal requirements offers a pathway to utilize low-grade industrial waste heat, drastically improving the process’s energy efficiency. Furthermore, the catalyst exhibited remarkable cyclic stability over ten consecutive cycles, maintaining its structural integrity and catalytic activity. These findings highlight β-FeOOH as an eco-friendly, cost-effective, and robust catalyst that aligns with the principles of green chemical engineering, offering a scalable strategy to enhance the sustainability of carbon capture operations. Full article

The DIGIT experiment was launched at the Tournemire Underground Research Laboratory (URL) with the aim of determining the effects of temperature on the transfer of tracers mimicking the most mobile radionuclides in the Toarcian clay rock. The properties of this rock are similar to those of the host rocks being considered for a future deep geological repository for high-level radioactive waste (HLW). The experiment involves the monitoring of the interaction between a test water doped with stable halides and deuterium at constant concentration, and the porewater of the Toarcian clay rock under constant ambient conditions, as well as at higher temperature induced by artificial heating. This experiment seeks to partially address questions regarding the potential spread of contaminants during the thermal phase of HL waste packages. Specifically, the in situ experiment aims to evaluate the role of scale effects, thermodiffusion, a process that combines Fick’s law, the Soret effect, and convection in the transfer of radionuclides. This paper is the second part of a companion paper dedicated to predictive calculations and the installation of the experimental device. It presents the main experimental and modeling results obtained since the beginning of the installation and after 20 months of heat at 70 °C. The test was carried out in five phases, finishing with a sampling campaign: a phase 0 called “initial conditions”, followed by a pure diffusion phase (5 months), then three phases in a heated period lasting 1 year and 8 months. In total, 47 rock cores were analyzed, with approximately 170 samples tested by four diffusion methods (radial, outgoing, through and in vapor-phase) to determine the tracer concentrations in the porewater, their water content and their diffusive transport parameters. The results show a decrease in tracer concentrations with distance from the test zone, in the directions parallel and perpendicular to the stratification. The anisotropy of the medium results in greater migration in the direction parallel to the stratification. Thermal properties also confirm anisotropy with a higher thermal conductivity in the direction parallel to the stratification. Finally, an activation energy of 22.9 ± 1.7 kJ·mol⁻¹ could be proposed by NMR for deuterium, indicating diffusion behavior following an Arrhenius law between 30 and 70 °C. The experimental data allowed for the calibration of a 2D axisymmetric numerical model using the commercial finite element software COMSOL Multiphysics^®. The Fick’s law corrected by an Arrhenius law best reproduces the penetration of deuterium and anions. The Soret effect, integrated into certain scenarios, is only significant for anions’ migration, using a fitted Soret coefficient of 0.1 K⁻¹, as proposed in the literature for the Callovo-Oxfordian, the host rock of the Cigéo project in the east of France. The calibration of the simulated data with the experimental data allowed for the characterization of damaged and/or disturbed zones evolving over time. Simulations over 150 years, the duration of the thermal maximum for HLW packages, show that advection—modeled by Darcy’s law—would have a negligible role in this context due to the low permeability of the upper Toarcian. In conclusion, the DIGIT test showed that, for the Upper Toarcian clay rocks at the Tournemire URL in France, diffusion, corrected for the effect of temperature, is the mechanism that characterizes the transport of radionuclide analogues. The study showed that thermodiffusion has a limited influence on deuterium migration but remains significant for anions in the case of a coupling between temperature correction and thermodiffusion. The test also highlighted the impact of temperature on the spatiotemporal development of a damaged and/or disturbed zone. These new and relevant results in the field will need to be confirmed later through additional experiments. Full article

Issues related to the environmental safety of transport vehicles, the operation of which leads to environmental pollution, continue to be highly relevant. In this work, we consider the use of biofuel mixed with diesel fuel for internal combustion engines operating at low temperatures. This approach does not reduce the efficiency of transport, while also solving the issue of organic waste recycling. In this work, we address the possibility of reducing environmental pollution using carbon-neutral blended fuels based on esters of waste cooking oil (WCO), biobutanol, and diesel fuel for transport, tractor, and other equipment powered by a diesel internal combustion engine. In terms of the rate of biofuel implementation, Russia is still lagging behind the EU, China, and Japan, largely due to, inter alia, its climatic conditions with cold and long winters. The article also provides data on the possibility of using mixed biofuels under sub-zero temperatures. The process of forming a volumetric fuel supply through the common rail injector of the D4CB engine under changes in fuel pressure and drive pulse duration was also investigated, with the corresponding regression dependencies being presented. The losses of heat supplied into the cylinder when using a blend of diesel fuel and biodiesel (with 20 wt% butanol) in comparison with diesel fuel were analytically calculated. This made it possible to identify a function for adjusting fuel supply to compensate for power losses. The lubricity of fuel blends was assessed using the HFRR method. Full article

The effective utilization and effective valorization of various organic industrial wastes have become increasingly important issues. One significant area for enhancing the circular economy is the processing of waste generated from vegetable oils and animal fats. This article focuses on the processing and use of soapstocks, which result from the chemical reaction between fatty acids and alkali. These soapstocks represent the most significant portion (approximately 70–90 wt% by weight) of waste produced by the oil and fat industry. The raw material for this study was soapstock obtained from the neutralization of sunflower oil at the PJSC “Zaporizhzhya Oil and Fat Plant,” designed by the Belgian company “De Smet.” The soapstock yield was found to be 9.95 wt% based on 100 wt% oil. Through a series of treatments involving water, acid, and multiple washes, a low-sulfur fuel component was produced that nearly meets the standards for boiler fuels as outlined in DSTU 4058-2001 and PN-C-96024:2020, except for the heat of combustion. It fully complies with the requirements specified in ISO 8217:2024. The sulfur content of the final product was determined to be 0.12 wt%. Additionally, the fuels produced contained 75.33 wt% carbon, 11.64 wt% hydrogen, and 12.00 wt% oxygen. Due to the relatively low oxygen content, the resulting product exhibits approximately twice the heat of combustion of similar fuels derived from other waste streams in the oil and fat industry. Full article