Heating Rate Research Articles

Thermodynamic Analysis of a Marine Diesel Engine Waste Heat-Assisted Cogeneration Power Plant Modified with Regeneration Onboard a Ship

The objective of this study is to perform a thermodynamic analysis on a marine diesel engine waste heat-assisted cogeneration power plant modified with regeneration onboard a ship. The proposed system utilizes the waste heat from the main engine jacket water and exhaust gases to generate electricity and heat, thereby reducing the fuel consumption and CO2 emissions. The methodology includes varying different turbine inlet pressures, extraction pressures, and fractions of steam extracted from the turbine to evaluate their effects on the efficiency, utilization factor, transformation energy equivalent factor, process heat rate, electrical power output, saved fuel flow rate, saved fuel cost, and reduced CO2 emissions. The analysis demonstrates that the proposed system can achieve an efficiency of 48.18% and utilization factor of 86.36%, savings of up to 57.325 kg/h in fuel, 65.606 USD/h in fuel costs, and 180.576 kg/h in CO2 emissions per unit mass flow rate through a steam turbine onboard a ship.

N, P Dual-Doped Carbons as Metal-Free Catalysts for Hydrogenation.

The activation of molecule hydrogen (H2) by metal-free catalysts is always a challenge in the field of catalysis. Herein, a series of N, P dual-doped carbon catalysts were constructed by the pyrolysis of chitosan and phytic acid and utilized as metal-free catalysts for the hydrogenation of nitrobenzene. The characterization indicated that the doping of phosphorus atoms not only formed the species with catalytic activity for hydrogenation reaction but also promoted the doping of N. The experimental results indicated that their catalytic performance could be improved by the regulation of pyrolysis temperature and heating rate. CP-900-1 (pyrolysis at 900 °C with a heating rate of 1 °C/min) exhibited a promising catalytic activity with >99% nitrobenzene conversion. N, P codoping was the key factor to its catalytic performance. All results indicated that the excellent catalytic activity of CP-900-1 was attributed to the synergistic interaction among pyridinic N, P-C species, and graphitic N. This work provides an effective route for the rational design and construction of highly efficient metal-free catalysts for hydrogenation.

Effect of nano silicon nitride integration on the curing performance of DGEBA epoxy matrix at ambient temperature

Epoxy curing requires substantial thermal energy input and is constrained by the specimen’s scale, shape, and design, especially with autoclave processing. This challenge is addressed in the present study by incorporating Silicon Nitride (SiN) nanoparticles into an epoxy matrix to enhance curing efficiency at room temperature. High-resolution transmission electron microscopy (HR-TEM) demonstrated a uniform dispersion of nanofillers within the epoxy, indicating improved mechanical and thermal stress transfer between the matrix and the filler. The interphase thickness, determined to be 1.16 nm using Lipatov’s theory and differential scanning calorimetry (DSC) thermograms, suggests excellent matrix-filler interaction and a significant increase in cross-link density. Thermogravimetric analysis (TGA) revealed an increase in activation energy by 63 %, 101 %, and 113 % at heating rates of 10, 20, and 30 °C/min, respectively, indicating enhanced thermal stability of the nanocomposite. Additionally, the char yield increased by 7 %, 18 %, and 22 % at the same heating rates, signifying the formation of effective crosslinks, leading to a higher proportion of solid remnants rather than volatiles during degradation.

Effect of heat production on MHD natural convection transport of nanofluid flow via a vertical uniform perforated plate: An unsteady analysis

This article statistically investigates the impact of heat production on the unstable MHD natural convection transport of nanofluid flow via a perforated sheet. The ordinary differential equations (ODEs) are derived from the partial differential equations (PDEs) by using of the similarity transformation. The dimensionless ordinary differential equations (ODEs) may be numerically resolved with the help of the MATLAB ODE45 tool and the finite difference method (FDM) along with the shooting strategy. Four innovative water-based nanofluids such as TiO2, Cu, Al2O3, and Ag are considered nanoparticles. The numerical results have been explained for the role of numerous non-dimensional numbers or parameters such as heat generation or absorption (Q), nanoparticle volume fraction (φ), Dufour number (Df), Prandtl number (Pr), magnetic force parameter (M), Soret number (Sr), and Schmidt number (Sc) on the fluid flow, and heat and mass transfer rates. The fluid temperature drops but velocity is enhanced for higher amounts of Q. Copper nanoparticle volume fraction up to 4 % shows a rise in temperature, concentration, and velocity curves. Heat transfer rate ( − θ′(0)) diminishes by about 124 %, while the values of f′(0) promote by approximately 26 % owing to an increase in the values of Q (heat generation) from 1.0 to 2.0. The value of ( − θ′(0)) increases by 49 %, but f′0 decreases by 15 % due to a rise in Q (heat absorption) from -3.0 to -10.0. The local skin friction coefficient (f′(0)) diminishes by about 65.21 % due to an increase in the values of the magnetic force parameter (M) from 0.5 to 3.5 whereas the rate of heat and mass transfer remain unchanged. As φ increased from 0.01 to 0.04, the local skin friction coefficient (f′(0)) exhibited a 36 % increase, while the heat transport rate (θ′(0)) decreased around by 10 %. In conclusion, a comparison was made between our findings and those of the published research. The comparison indicates a high degree of consistency.

Modelling the ejection of primary aerosols during the fast pyrolysis of biomass anisotropic particles

A model for the fast pyrolysis of anisotropic biomass particles is presented which considers bubbling dynamics within the liquid intermediate phase (metaplast) and aerosol ejection from this phase. The model employs the population balance equation and the method of moments to estimate the production rate and resultant size distribution of aerosol ejections, incorporating a detailed CRECK reaction mechanism, and considers the effect of anisotropic biomass microstructure on the intraparticle transport of mass and energy. This study investigates the impact of particle size, heating rate (heat transfer coefficient), and lignocellulosic composition on aerosol ejection. The model predicts that, at high heating rates (convective heat transfer coefficient of 359 W/m2.K), aerosols can contribute over 20% to the heavy fraction yield in bio-oil for small particles (1 mm diameter, 4 mm length). The model can predict aerosol size distribution and surface area, indicating an average size of 20 μm for bubbles and 5 μm for aerosols during increased bubble production and aerosol ejection rates. These findings are consistent with prior experimental results and provide essential information for future modeling of extra-particle reactions of the aerosols as they progress through the reactor.

Polymer‐Sorbent Direct Air Capture Contactors with Complex Geometries 3D‐Printed via Templated Phase Inversion

AbstractLow‐cost direct air capture (DAC) systems require efficient gas–solid contactors. These contactors provide rapid rates of heat and mass transport with minimal pressure drops. Triply periodic minimal surfaces (TPMS) are a class of geometries that are shown to have heat transfer properties that exceed those of other geometries, and these benefits are expected to manifest in mass transfer as well due to the analogies between heat and mass transfer. However, creating TPMS contactors is difficult using conventional manufacturing techniques such as injection molding. Non‐solvent‐induced phase separation (NIPS) of a polymeric ink containing the adsorbent is one way to construct adsorption contactors with excellent mass transport rates, but contactors have to date only been fabricated in simple geometries (e.g., films, fibers). This study demonstrates that NIPS of polymeric inks occurs within a simultaneously‐dissolving, water‐soluble, 3D‐printed template. This templated phase inversion (TPI) technique can create seemingly unlimited macroscopic architectures, including TPMS contactors, using a variety of potential DAC adsorbents, including zeolite, silica, activated carbon, and metal–organic frameworks. SEM, micro‐computed tomography, and nitrogen adsorption experiments reveal the microscopic pore structures and macroscopic geometries of the resulting sorbent contactors. TPMS DAC contactors with poly(ethyleneimine)/silica adsorbents are shown to have CO2 capture performances that rival or exceed other contactor geometries.

Insights into catalytic co-pyrolysis of spent coffee grounds and high density polyethylene (HDPE) using acid mine drainage (AMD) treated sludge based catalyst: Analysis of kinetics, mechanism and thermodynamic properties

The present study aims to investigate the catalytic effect of acid mine drainage (AMD) treated sludge based catalyst on the co-pyrolysis of spent coffee grounds and HDPE. The sludge was generated during the treatment of AMD using eggshell and hydrogen peroxide. Theromogravimetric analysis of pyrolysis of spent coffee grounds (SC), HDPE (High density polyethylene), blend of spent coffee grounds and HDPE (SC+HDPE) in the ratio of 1:1, and blended feedstock with sludge derived catalyst (SC+HDPE_AMDC) (1:1 wt. ratio) was conducted at various heating rates of 10 °C/min, 20 °C/min, 30 °C/min and 40 °C/min respectively. Iso-conversional models such as Ozawa Flynn Wall (OFW), Kissinger Akahira Sunose (KAS), Friedman, and Starink were utilized for the determination of activation energy (Ea) of the process. The results showed that using AMD treated sludge based catalyst to the pyrolysis process, enhances its overall efficacy by lowering the activation energy (Ea) (OFW- Ea: 209.11 to 177.14 KJ/mol, KAS-Ea: 208.30 to 173.06 KJ/mol, Friedman- Ea:210.54 to 176.28 KJ/mol, and Starink- Ea:208.60 to 173.44 KJ/mol). Criado's z-master plot (CZMP) method was utilized to analyze the mechanism of the reaction. The pre-exponential factor and thermodynamic parameters were also evaluated. It is concluded that the incorporation of sludge based catalyst (AMDC) lowered enthalpy and randomness of system. Catalytic co-pyrolysis requires less energy, making it more environmental friendly choice for the sustainable processing of biomass and plastics. The present investigation will aid in the design, optimization and scalability.

Pyrolysis and Physicochemical, Thermokinetic and Thermodynamic Analyses of Ceiba aesculifolia (Kunth) Britt and Baker Waste to Evaluate Its Bioenergy Potential.

Ceiba aesculifolia is an important species in Mexico that generates significant amounts of biomass waste during its exploitation, which can be utilized to produce energy. This study presents the characterization of this waste based on chemical (proximal and elemental) and thermal analyses (TGA-DTG) at different heating rates (β = 10-30 °C/min (283-303 K/min)) in the presence of nitrogen and in a temperature range of 25-900 °C. Kinetic parameters were calculated and analyzed as well. Activation energy (Ea) and the pre-exponential factor (A) were determined using the Friedman (132.03 kJ/mol, 8.11E + 10 s -1), FWO (121.65 kJ/mol, 4.30E + 09), KAS (118.14 kJ/mol, 2.41E + 09), and Kissinger (155.85 kJ/mol, 3.47E + 11) kinetic methods. Variation in the reaction order, n (0.3937-0.6141), was obtained by Avrami's theory. We also calculated the thermodynamic parameters (ΔH, ΔG, ΔS) for each kinetic method applied. The results for Ea, A, n, ΔH, ΔG, and ΔS show that this biomass waste is apt for use in pyrolysis. Moreover, the moisture (<10%), ash (<2%), volatile material (>80%), and HHV (>19%) contents of C. aesculifolia allowed us to predict acceptable performance in generating energy and fuels. Finally, infrared spectroscopy analysis (FT-IR) allowed us to identify important functional groups, including one that belongs to the family of the aliphatic hydrocarbons.

Manufacturing of heavy tungsten alloys from nano-sized metal oxides via simultaneous reduction-sintering powder treatments

Heavy tungsten alloys are of great importance in the engineering and mining industries as well as the military and medical applications because of their stability at high temperatures, high strength and dense structures. The present study develops a novel technology for the production of heavy tungsten alloys via thermal treatment of nano-sized metal oxides based on simultaneous reduction and sintering processes. Heavy tungsten alloy (95W-3Ni-2Fe) was produced from the reduction of mixed nano-sized metal oxides precursor in H2 at 1000 o C followed by sintering at 1350–1450 o C for 30–90 min. The reduced and sintered samples were characterized by XRD to follow up the crystallinity, total porosity measurement was used to find out the densification properties, the grain structure and morphology were examined by RLM and SEM attached with EDAX. Micro-hardness tester was also used to investigate the influence of sintering conditions on the grain densification. A fundamental study on the kinetics of reduction of mixed nano-sized metal oxides precursor was performed by isothermal and non-isothermal techniques. Both results from isothermal and non-isothermal tests were used to calculate the activation energy which was correlated with macro- and micro-structures to predict the corresponding reduction mechanism. However, the influence of sintering temperature and time on the crystallinity of the produced phases, grain structure, morphology, total porosity, pore-size distribution, bulk and apparent densities, and the hardness of sintered compacts was extensively investigated. The results revealed that the presence of NiO and/or Fe2O3 in the mixed metal oxides precursor was very important to ease the reducibility of WO3 as the metallic phases of Ni and/or Fe act as a catalyst for the reduction of WO3. The rate of reduction proceeds faster in the following order: NiO > Fe2O3 > mixed oxide > WO3. In non-isothermal experiments, it was found that the heating rate has a considerable effect on the reduction of precursor, i.e., the lower the heating rate, the higher the degree of reduction. It might be reported that the use of nano-sized metal oxides particles in the fabrication of heavy tungsten alloys greatly affects the main properties of the produced alloy. With the increase in sintering time, larger sizes of dense grains were developed, and the matrix became denser as a result of sintering and re-crystallization effects. The higher the sintering time, the higher the grain densification and the less pores formed in the matrix. On the other hand, with the increase in the sintering temperature, the grain boundaries were well defined in which the grains were composed of tungsten metal and surrounded by inter-metallics. The higher the temperature, the higher the XRD peak intensities of metallic tungsten and intermetallics as a result of sintering and re-crystallization.

Effect of Sintering Temperature on the Microstructure and Mechanical and Tribological Properties of Copper Matrix Composite for Brake Pads

Copper-based powder metallurgy materials are frequently utilized in fabricating brake pads for high-speed trains. The preparation process involves mixing, ball milling, pressing, and sintering. Among these steps, hot-pressed sintering stands out as a rapid and efficient method that significantly influences the properties and performance of the products. In this study, four samples (S700/S750/S800/S850) were prepared using hot-pressed sintering at various temperatures, as follows: 700 °C, 750 °C, 800 °C, and 850 °C. The mechanical and physical properties of the four samples were tested, and the microstructure and compositions were investigated using scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction. The findings highlighted the close relationship between sintering temperature and the mechanical and physical properties of the samples, as it impacts the porosity and interfacial bonding of the particles. Notably, Sample S800 demonstrated superior mechanical and thermal conductivity. Furthermore, the coefficient of friction (COF), friction heat, and wear rate of the four samples were also tested under different braking speeds ranging from 150 km/h to 350 km/h. The results indicated that the COFs of the four samples remained relatively stable below 300 km/h but decreased notably above 300 km/h due to heat fading. Sample S800 displayed consistent and high COF under varied braking speeds and exhibited the lowest wear rate. The observed wear mechanisms included abrasive wear and oxidation wear. Additionally, the friction test results underscored the close correspondence of the COF curve of S800 with the standard of the Ministry of Railways of the People’s Republic of China.

Organic compounds as temperature calibrants for fast scanning calorimetry

Organic compounds can be used as temperature calibrants in fast scanning calorimetry. Their advantages include ease of surface cleaning of the calorimetric chip and good thermal contact with the chip surface. Among several compounds tested, benzoic acid was identified as a convenient and reliable calibrant for temperatures below approximately 130 °C. However, organic calibrants often exhibit unusual heating rate dependencies of the onset temperatures of melting. This phenomenon can be semi-quantitatively explained by considering different heat flows within the sensor. Notably, the thermal resistance between the heater and thermopile, often overlooked, introduces an additional time constant that can sometimes result in a negative apparent thermal lag. In addition, the onset temperatures are influenced by factors such as sample position, thickness, surface wetting, and spreading. These factors limit the accuracy of transition temperature determinations to approximately ±1 K below 130 °C and ±5 K up to 220 °C.

Sintering trials and microstructural changes mechanism of analogues of americium oxides for radioisotope power systems

Radioisotope thermoelectric generators (RTGs) are deal energy supply devices for deep space and deep-sea exploration, and it is also the energy core of the operation of the working equipment. Except for 238Pu (Plutonium), 241Am (Americium) was also used as a nuclide in the radioactive energy system for future space exploration missions. In this work, neodymium oxide (Nd2O3) was used as analogues for Am2O3. Cold-press-and-sinter methods was used. Different particle parameters (morphology, size, and crystal structure) and synthesized parameters of Nd2O3 were investigated. The synthesized powders contained lath-shaped particles, and batches with different particle sizes and microscopic topography were made and sintered. The results show that the optimal precipitation temperature of Nd2O3 is 25 °C. The optimal thermal decomposition temperature range is 900 °C to 1100 °C, and the optimal thermal decomposition heating rate is 10 °C min−1. The samples of Nd2O3 pellets without cracking is obtained with relative density of 85%–90 %. The Vickers hardness of Nd2O3 pellets was also studied. This paper provides an important scientific guiding significance for the cold-press-and-sinter of radioisotope 241Am batteries in the future.

Exploring Corymbia torelliana hydrochar combustion kinetics through thermogravimetric analysis, peak deconvolution and reaction profile modelling.

This study aims to conduct an applied and innovative investigation to enhance the energy quality of wood residues through hydrothermal carbonization pretreatment. For this purpose, the treatment was carried out at three different temperatures: 180, 220, and 240°C under autogenous pressure. The in natura material and the hydrochars were characterized, and thermogravimetric analyses were performed in an O2 atmosphere with heating rates of 2.5, 5, 10, and 20°Cmin-1. The global activation energy for natura biomass combustion was determined to be 112.49kJ.mol-1. On the other hand, the hydrothermal carbonization process promoted a reduction in this value for the 94.85kJ.mol-1. The conversion function for the in natura biomass was characterized as , order 1, while the hydrochars was 2(1-α) [-ln(1-α)] (1⁄2), Avrami-Erofe'ev I. Triple kinetic parameters were ascertained, and the conversion curves along with their respective derivatives were modeled, exhibiting minimal deviations between theoretical and experimental data. This facilitated the mathematical representation of the reaction processes and allowed for a comprehensive comparison of the results.

Properties of biocoal briquettes from mesoporous coals and rice husk and their effects on environmental pollution

This work assessed some properties and effects of biocoal briquettes on environmental pollution compared with utilising coal alone. A mixture of coal fines and rice husks was prepared, with cassava starch gel as a binder, before compaction in a briquetting machine and drying with a solar dryer. Samples of the coal fines, rice husk, cassava flour and briquettes were analysed for their elemental and oxide concentrations via an energy-dispersive X-ray fluorescence analyser. The heat fuels were analysed for their thermal behaviour via thermogravimetric analyser (TGA), whereas the specific surface area, pore size and pore volume were determined using a Brunner–Emmett–Teller (BET) analyser. The conversion of the tested coals to biocoal briquettes resulted in a reduction in the level of arsenic in the briquettes. Additionally, the sulphur level decreased from 1.96 to 1.11% in the Okobo-Enjema briquettes and from 1.78 to 0.90% in the Onyeama briquettes. However, the levels of manganese increased from 0.04 to 0.22% in the Okobo-Enjema briquettes and from 0.04 to 0.21% in the Onyeama briquettes. Thermogravimetric analysis at different heating rates revealed that derivative weight loss increased with increasing heating rate, from 4.4% at 10 °C/min to 5.5% at 20 °C/min. BET analysis revealed that the briquettes had larger pore diameters, volumes and specific surface areas than did the coal samples. The coal samples have greater propensity to pollute the environment as the amount of potentially hazardous elements in the samples is greater than in their biocoal briquettes.

Analysis of curing deformation for resin matrix composite T-shaped stiffened panel

In this work, a multi-field coupled finite element simulation method involving thermochemistry and mechanics was devised to predict the curing deformation (C-DE) of a T-shaped stiffened panel (T-SSPL), a typical aircraft structural component, during the autoclave forming process. A more comprehensive and detailed analysis of the factors affecting the C-DE of T-SSPL is also carried out. The methodology uses the Fortran language to write different user subroutines and establish corresponding mathematical models to simulate the different mechanical states of components, and ultimately simulate the entire molding process of the product in the autoclave. And investigates the effects of process parameters, including heating rate, cooling rate, curing pressure, and structural parameters, including the number of bars and height of stringer on the C-DE of T-SSPL, and obtains the following conclusions: the heating rate and curing pressure are positively correlated with the C-DE, and the cooling rate has little influence on the C-DE, and C-DE hardly changes with the change of cooling rate; C-DE increases with the ribs count; however, it decreases and then increases with the stringer height, and these conclusions provides a theoretical basis for the manufacturing of T-SSPL.

Nanoengineered Injectable Hydrogel: An Advanced Radioprotective Barrier with Magnetic Hyperthermia Synergy.

Despite its effectiveness in eradicating cancer cells, current tumor radiotherapy often causes irreversible damage to the surrounding healthy tissues. To address this issue and enhance therapeutic outcomes, we developed a multifunctional injectable hydrogel that integrates electromagnetic shielding and magnetothermal effects. This innovation aims to improve the efficacy of brachytherapy while protecting adjacent normal tissues. Recognizing the limitations of existing hydrogel materials in terms of stretchability, durability, and single functionality, we engineered a composite hydrogel by self-assembling nickel nanoparticles on the surface of liquid metal particles and embedding them into an injectable hydrogel matrix. The resulting composite material demonstrates superior electromagnetic interference shielding performance (74.89 dB) and a rapid magnetothermal heating rate (10.9 °C/min), significantly enhancing its in vivo applicability. The experimental results confirm that this innovative nanocomposite hydrogel effectively attenuates electromagnetic waves during brachytherapy, thereby protecting normal tissues surrounding the tumor and enhancing radiotherapy efficacy through magnetothermal therapy. This study advances the safety and effectiveness of cancer treatments and provides new insights into the development of multifunctional biomedical materials, promoting the innovative application of nanotechnology in the medical field.

The effect of pyrolysis heating rate on the mesoporosity of Pluronic F-127 templated carbon xerogels

This study explored the impact of pyrolysis heating rates ranging from 1 to 20 K min−1 (final temperature 500 °C) on the porosity of resorcinol-formaldehyde based carbonaceous xerogels soft-templated with Pluronic F-127. We primarily utilized thermoporometry (differential scanning calorimetry technique) and, to a lesser extent, conventional nitrogen adsorption at −196 °C to analyze the porosity of the resulting carbons. Additionally, we examined the effects of particle size and the scale of the pyrolysis experiment, comparing a laboratory furnace with a thermal analyzer. At lower heating rates, particularly in a thermal analyzer, mesopores approximately 7–8 nm in size were observed. An increase in the heating rate resulted in larger mesopores, from 7 to 17 nm, widened pore size distribution (PSD), and a rise in mesopore volume from 0.21 to 0.53 cm3g−1. Higher heating rates (> 5 K min-1) also accelerated the decomposition of the Pluronic F-127, leading to fast gas release, which subsequently caused cracking of the carbon skeleton and widening of the pores. Pyrolysis heating rate had no significant effect on the degree of graphitization in the pyrolyzed samples. Particle size showed minimal influence on porosity when xerogels were pyrolyzed at either the minimal or maximal heating rates in the thermal analyzer. However, experiments conducted in a laboratory furnace at the lowest heating rate demonstrated that imprecise temperature control and fluctuations can lead to the formation of larger mesopores.

Combined kinetic analysis of thermal degradation characteristics and reaction mechanism of thin intumescent fire-retardant coating of steel structure

To determine the thermal kinetic triplets and elucidate the reaction mechanism of thin intumescent fire-retardant coatings (IFR) of steel structures, one efficient combined kinetic approach was implemented in this study. Thermogravimetric experiments were conducted in air atmosphere at four heating rates, and the whole IFR thermal degradation process was divided into two stages. The average activation energy values derived by model-free methods were 78.9 kJ/mol and 175.16 kJ/mol for Stage I (0<α < 0.2) and Stage II (0.2<α < 0.9), respectively. Furthermore, the linear Coats-Redfern (CR) and non-linear Masterplots models were applied to identify the possible reaction mechanism. It was found that the F3/2 mechanistic model was better suited to the main thermal degradation process. Then model reconstruction based on the F3/2 mechanism model was performed. The results showed that the reconstructed model had a strict linear relationship in the independence analysis and KCE analysis, along with a good agreement between the theoretical and experimental results. The current study provided new insights into the systematic thermal degradation mechanism of IFR, and the proposed kinetic model would be helpful for the thermal protection prediction for steel structure during fire.

Thermoluminescence (TL) properties of Eu3+ incorporated with CaB4O7 phosphors prepared by solution-combustion process

The solution-combustion approach was used to create CaB4O7:Eu3+phosphors using Ba (NO3)2, Eu (NO3)3·5H2O, H3BO3, NH3(ON)H2, and NH4NO3 as source materials. We investigated the thermoluminescence (TL) characteristics of beta (β)-irradiated CaB4O7:Eu3+. When the TL intensity was evaluated at different dosages of β, it rose with the dose. Changes in peak temperature were observed because of the investigation of the effects of varying heating rates on TL glow curves. Moreover, the positions of the peak temperature and the TL intensity did not change when the same sample was measured again, suggesting that the sample was stable. Additionally, the study calculated several kinetic parameters, including activation energy (E), frequency factor (s), and geometrical factor (μg), for distinct TL glow curves. Through geometric analysis of TL glow peaks, the study determined activation energies and kinetic orders, enabling the calculation of the frequency factor. The findings highlight the suitability of the prepared phosphor for dosimetry and provide insights into trap characteristics crucial for continuous illumination at room temperature. The study also emphasises the importance of optimising trap depth for prolonged afterglow, shedding light on the interplay between trap energies and luminescence characteristics. These findings deepen our comprehension of phosphor behavior and open the door to better dosimetry applications.

Performance Properties and Finite Element Modelling of Forest-Based Bionanomaterials/Activated Carbon Composite Film for Sustainable Future

Thanks to its highly crystalline structure and excellent thermal, optical, electrical and mechanical properties, carbon and its derivatives are considered the preferred reinforcement material in composites used in many industrial applications, especially in the forest and forest products sector, including oil, gas and aviation. Since hydroxyethyl cellulose (HEC) is a biopolymer, it has poor mechanical and thermal properties. These properties need to be strengthened with various additives. This study aims to improve the thermal and mechanical properties of hydroxyethyl cellulose by preparing hydroxyethyl cellulose/activated carbon (HEC/AC) composite materials. With this study, composites were obtained for the first time and their mechanical properties were examined using a 3D numerical modeling technique. The thermal stability of the prepared composite materials was investigated via thermal gravimetric analysis (TGA). The samples were heated from 30 °C to 750 °C with a heating rate of 10 °C/min under a nitrogen atmosphere and their masses were measured subsequently. The mechanical properties of the composites were investigated via the tensile test. The viscoelastic properties of the composite films were determined with dynamic mechanical thermal analyses (DMTA) and their morphologies were examined with scanning electron microscopy (SEM) images. According to the results, the best F3 sample (films containing 3 wt.% activated carbon) had an elastic modulus of 168.3 MPa, a thermal conductivity value of 0.068 W/mK, the maximum mass loss was at 328.20 °C and the initial storage modulus at 30 °C was 206.13 MPa. It was determined that the hydroxyethyl cellulose composite films containing 3 wt.% activated carbon revealed the optimum results in terms of both thermal conductivity and viscoelastic response and showed that the obtained composite films could be used in industrial applications where thermal conductivity was required.