Increase In Thermal Conductivity Research Articles

Excellent thermal conductivity and electrical insulation in polyimide/graphene oxide/carbon nanotubes composites

AbstractPolymer composites with heat resistance, good thermal conductivity, and insulation properties can meet the special needs of electronics and electrical appliances. In this work, graphene oxide (GO) and carbon nanotubes (CNTs) are coated by polydopamine (PDA). 4,4′‐diaminodiphenyl ether (ODA), pyromellitic dianhydride (PMDA), and 4,4′‐oxydiphthalic anhydride (ODPA) in‐situ polymerize to prepare poly(amide acid) (PAA) containing thermally conductive yet insulating fillers (PDA@GO, PDA@CNTs). As the concentration of fillers in PI composites increases, the thermal conductivity rises, but the insulation property decreases. Keeping the filler content constant and varying the ratio of PDA@GO and PDA@CNTs, the thermal conductivity increases and then decreases. When PDA@GO and PDA@CNTs have a mass ratio of 10:1, the significant synergistic effect affects the thermal conductivity. The PI/PG10C1–25 sample has a thermal conductivity of 1.46 W/(m·K), which is 6.9 times greater than the pure PI. Additionally, the volume resistivity, dielectric permittivity, and dielectric loss (100 kHz) of PI/PG10C1–25 are 2.8 × 1013 Ω cm, 5.4 and 0.28, respectively. The heat resistance of PI composites is almost the same as that of pure PI. Given these outstanding attributes, the developed PI composites offer vast applications in many fields.Highlights Synergistic PDA@GO and PDA@CNTs (10:1) optimize thermal conductivity. PI/PG10C1–25 achieves 6.9 times higher thermal conductivity than pure PI. Volume resistivity of PI/PG10C1–25 reaches 2.8 × 1013 Ω·cm. Dielectric permittivity of PI/PG10C1–25 reaches 5.4 at 100 kHz. Developed PI composites maintain excellent heat resistance.

Evaluation of carbonized cotton stalk for development of novel form stable composite phase change materials for solar thermal energy storage

Generating energy from the renewable sources is a pathway to attain sustainable energy systems. Utilizing bio-char produced from pyrolysis process as porous material would not only add great value to the waste discards, but also contributes towards enhancing the thermal properties. This work is focussed on the development of form stable phase change material (FSPCM) through a facile impregnation method by introducing cotton stalk biochar (CSB) as porous matrix along with polyethylene glycol having molar mass 10000 g/mol (PEG10000) as PCM. Cotton stalk is an agriculture waste material and biochar was produced by intermediate pyrolysis method at 550 °C. Thermal, chemical and surface characterization tests were executed on seepage free FSPCM (BCPCM4) as it showed no leakage at 60 °C. XRD, FTIR, FESEM, TGA, DSC, Raman spectroscopy and BET analysis were carried out to characterize thermal, chemical and surface properties of BCPCM4. The microporous structure of CSB was able to accommodate 80 wt% of PEG10000. Surface characterization tests demonstrated that adequate amount of PEG10000 was absorbed into the pores of CSB and the crystal structure of PEG10000 was not modified. The results of TGA illustrated that BCPCM4 was thermally stable. Additionally, cotton stalk derived FSPCM displayed high heat transfer rate which indicates an increase in thermal conductivity. To substantiate thermal reliability, 500 thermal cycles were run on BCPCM4 and about 1 % variation in latent heat has been noticed with meagre change in chemical properties. Therefore, biochar derived FSPCMs would serve as promising materials to accommodate solar thermal energy.

Hydrophobic Modification of Pectin Aerogels via Chemical Vapor Deposition.

Pectin aerogels, with very low density (around 0.1 g cm-3) and high specific surface area (up to 600 m2 g-1), are excellent thermal insulation materials since their thermal conductivity is below that of air at ambient conditions (0.025 W m-1 K-1). However, due to their intrinsic hydrophilicity, pectin aerogels collapse when in contact with water vapor, losing superinsulating properties. In this work, first, pectin aerogels were made, and the influence of the different process parameters on the materials' structure and properties were studied. All neat pectin aerogels had a low density (0.04-0.11 g cm-1), high specific surface area (308-567 m2 g-1), and very low thermal conductivity (0.015-0.023 W m-1 K-1). Then, pectin aerogels were hydrophobized via the chemical vapor deposition of methyltrimethoxysilane using different reaction durations (2 to 24 h). The influence of hydrophobization on material properties, especially on thermal conductivity, was recorded by conditioning in a climate chamber (25 °C, 80% relative humidity). Hydrophobization resulted in the increase in thermal conductivity compared to that of neat pectin aerogels. MTMS deposition for 16 h was efficient for hydrophobizing pectin aerogels in moist environment (contact angle 115°) and stabilizing material properties with no fluctuation in thermal conductivity (0.030 W m-1 K-1) and density for the testing period of 8 months.

Experimental study on solar wall by considering parametric sensitivity analysis to enhance heat transfer and energy grade using compound parabolic concentrator and pulsating heat pipe

Enhancing high-grade and rapid thermal storage for solar energy utilization is of paramount importance in reducing building energy consumption. Therefore, this study combines the Compound Parabolic Concentrator (CPC) and Pulsating Heat Pipe (PHP) to propose an integrated CPC-PHP solar wall (CPC-PHP-SW) that can enhance solar energy grade and rapid thermal storage. The mixed working fluid for CPC-PHP-SW is developed to reduce the dependence on solar radiation intensity and facilitate PHP startup. Furthermore, the operating characteristics and heat transfer performances of the CPC-PHP-SW are studied experimentally under various factors, including solar radiation intensity, working fluid, and cooling temperature. Sensitivity analyses of these three factors on heat transfer performances are conducted using Multi-factor analysis of variance. Results highlight that solar radiation intensity is the most influential factor on heat transfer performance, followed by cooling temperature, and working fluid. Moreover, employing a CPC with a concentration ratio of 2 reduces thermal resistance by up to 56.46 %, while the maximum effective thermal conductivity increases by up to 129.65 %. A recommended methanol to water ratio is 1:3, which effectively copes with a wide range of solar radiation intensity. These findings provide valuable references for the design and application of CPC-PHP-SW in building envelopes.

Crystal structure, stability, and transport properties of Li2BeAl and Li2BeGa Heusler alloys: a DFT study

In this study, the structural, elastic, electronic, and thermoelectric properties of full Li2BeAl and Li2BeGa Heusler alloys were explored using density functional and the Boltzmann transport theories. The GGA and HSE approximations have been used for the exchange–correlation potential. Results indicated that these two compounds are more energetically stable in the inverse Heusler structure. Additionally, both Li2BeAl and Li2BeGa Heusler alloys were found to be mechanically stable due to the positive values of the elastic constants. Also, the high values of the Young's modulus indicate that these compounds are stiff and exhibit a semi-metallic nature. The band gaps were determined to be 0.13 eV and − 0.22 eV for Li2BeAl and Li2BeGa alloys, respectively, using the GGA approximation. By employing the HSE hybrid functional, however, the band gap for Li2BeAl increased to 0.26 eV, and for Li2BeGa, it decreased to − 0.16 eV. Regarding thermoelectric properties, Seebeck coefficient, electrical conductivity, electronic and lattice thermal conductivities, power factor, and the figure of merit have been calculated for both Li2BeAl and Li2BeGa Heusler alloys at different temperatures. Seebeck coefficient in both alloys decreases with increasing the temperature and has the highest value at 300 K. Thermal conductivity and electrical conductivity increase with increasing the temperature, which confirms the intermetallic behavior of the Heusler alloys. The results obtained for both alloys show that n-type doping has better thermoelectric properties than p-type doping. The maximum value of the figure of merit (ZT) was obtained for n-type doping, which was 1.43 at 660 K for Li2BeAl and 0.39 at 1000 K for Li2BeGa alloy. The high values of ZT especially for electron-dopped Li2BeAl suggest the great potential of this material for use in thermoelectric devices. This study suggests that the proposed materials have potential applications in spintronic devices and thermoelectric materials due to their intermetallic character and effective thermoelectric coefficients.

Molecular dynamic modeling and analysis of the sintering behaviors of GDC modified BSCF nanorods for rSOC oxygen electrode

Degradation including segregation and high stress related issues are significant challenges for reversible solid oxide cells (rSOCs), particularly concerning the oxygen electrode. Understanding the sintering preparation is crucial for enhancing the performance and reliability of the oxygen electrode under long-term dual-mode operation. In this study, the sintering process of Ba0.5Sr0.5Co0.8Fe0.2O3-δ nanorods anchored with Gd-doped CeO2 nanoparticles (GDC-BSCF-NR) was predicted by using molecular dynamics method. To optimize the sintering process, the stress distribution, A-site ion migration behavior and thermal properties of the composite electrode materials were analyzed at different sintering temperature, the effects of nanoparticle size were also investigated. Both thermal conductivity and thermal expansion increase with sintering temperature. The particle stress of the composites correlates positively with the diffusion coefficient of ions. The diffusion coefficients of surface and internal Ba/Sr ions increase by 6%–9% from 973 K to 1373 K, while stress increases by 19%–33 %. The diffusion coefficient of BSCF particles decrease by 15.1 % with an increase in GDC nanoparticle size, which is beneficial for suppressing Ba/Sr segregation.

Preparation and properties of three-dimensional continuous network reinforced Graphite/SiC ceramic composite insulation materials

Addressing the challenge of existing insulation materials struggling to achieve the synergy of lightweight construction, high strength, and low thermal conductivity, this paper presents a method based on multi-material assembly technology to achieve a controlled composite of a three-dimensional continuous silicon carbide network and graphite matrix. Following an examination of the impact of various forming densities and the addition of expandable graphite on the thermal conductivity and compressive strength of graphite/SiC composites, the study explored the effects of different "enhancement network" topologies on the properties of these composites. The investigation demonstrates that adjusting the forming density and incorporating expandable graphite enable regulation of both the porosity and closed porosity of the composites, thereby controlling their compressive strength and thermal conductivity. Additionally, the construction of a three-dimensional continuous SiC network structure within the graphite matrix significantly enhances the compressive strength of the composites, with only a slight increase in thermal conductivity. A graphite/SiC composite thermal insulation material was ultimately developed, boasting a density of merely 1.1 g/cm³, a low thermal conductivity of 1.847 W/m·K, and an impressive compressive strength reaching 15.627 MPa. Its overall performance surpasses that of water-glass sand, making it a promising candidate for various applications in the foundry industry as a thermal insulation material.

Prestrain Guided Yield of Large Single-Crystal Nickel Foils with High-Index Facets.

Single-crystal metal foils with high-index facets are currently being investigated owing to their potential application in the epitaxial growth of high-quality van der Waals film materials, electrochemical catalysis, gas sensing, and other fields. However, the controllable synthesis of large single-crystal metal foils with high-index facets remains a great challenge because high-index facets with high surface energy are not preferentially formed thermodynamically and kinetically. Herein, single-crystal nickel foils with a series of high-index facets are efficiently prepared by applying prestrain energy engineering technique, with the largest single-crystal foil exceeding 5×8 cm2 in size. In terms of thermodynamics, the internal mechanism of prestrain regulation on the formation of high-index facets is proposed. Molecular dynamics simulation is utilized to replicate and explain the phenomenon of multiple crystallographic orientations resulting from prestrain regulation. Additionally, large-sized and high-quality graphite films are successfully fabricated on single-crystal Ni(012) foils. Compared to the polycrystalline nickel, the graphite/single-crystal Ni(012) foil composites show more than five-fold increase in thermal conductivity, thereby showing great potential applications in thermal management. This study hence presents a novel approach for the preparation of single-crystal nickel foils with high-index facets, which is beneficial for the epitaxial growth of certain two-dimensionalmaterials.

Effect of ten different physical parameters on solar still productivity: Theoretical modeling

AbstractSolar distillation using solar stills is widely recognized as a clean and cost‐effective method for producing freshwater. However, due to its straightforward design, solar still performance is greatly influenced by various physical characteristics. Many researches have evaluated solar still parameters, while only a few articles have concerned physical ones. Therefore, this article aims to investigate the effect of different physical parameters on solar still productivity through thermal modeling. The theoretical results were validated with those of a previous experimental model, showing a good agreement with each other. The results reveal that daily productivity experiences significant improvement with an increase in plate emissivity or insulation thickness. Conversely, an increase in water mass, glass absorptivity or insulation thermal conductivity leads to a substantial reduction in productivity. Notably, water transmissivity and plate absorptivity do not affect productivity. Modest enhancements in productivity can be achieved by reducing the effective emissivity between water and glass. While the initial temperature of water has a minor impact on productivity at low water mass, it exhibits a substantial improvement effect at high water mass. These results can be a good guidance for the designers and manufacturers to develop more efficient designs that maximize the production of clean water.

Microstructure and properties of Cu/Si composites for electronic packaging: Effect of tungsten layer on silicon particles

Cu/Si composite are ideal electronic packaging materials, but the intense formation of Cu-Si intermetallics during preparation leads to a significant decrease in their plasticity and thermal conductivity. In this paper, a W layer was formed on Si particles using the sol-gel method, and Cu/Si composites were prepared by hot pressing. The results show that the maximum thickness of the W layer is 1.64 μm, and the minimum thickness is only 809 nm. The W layer acts as a diffusion barrier, effectively inhibiting the Cu-Si interfacial reaction and intermetallics formation, thus preventing the deterioration of matrix and reinforcement properties. Compared with the Cu/Si composite, the elongation of the Cu/Si@W composite improves from 0.2 % to 1.7 %, and the thermal conductivity increases by 7 times to 233.9 W/(m·K). Additionally, among the four samples, the Cu/Si@W composite has the lowest coefficient of thermal expansion (CTE). The W layer enhances the mechanical properties and thermal conductivity while reducing the CTE of Cu/Si composite for improved electronic packaging application.

Enhancing the Conductivity and Thermoelectric Performance of Semicrystalline Conducting Polymers through Controlled Tie Chain Incorporation.

Conjugated polymers are promising materials for thermoelectric applications, however, at present few effective and well-understood strategies exist to further advance their thermoelectric performance. Here a new model system is reported for a better understanding of the key factors governing their thermoelectric properties: aligned, ribbon-phase poly[2,5-bis(3-dodecylthiophen-2-yl)thieno[3,2-b]thiophene] (PBTTT) doped by ion-exchange doping. Using a range of microstructural and spectroscopic methods, the effect of controlled incorporation of tie-chains between the crystalline domains is studied through blending of high and low molecular weight chains. The tie chains provide efficient transport pathways between crystalline domains and lead to significantly enhanced electrical conductivity of 4810 S cm-1, which is not accompanied by a reduction in Seebeck coefficient or a large increase in thermal conductivity. Respectable power factors of 173 µW m-1 K-2 are demonstrated in this model system. The approach is generally applicable to a wide range of semicrystalline conjugated polymers and could provide an effective pathway for further enhancing their thermoelectric properties and overcome traditional trade-offs in optimization of thermoelectric performance.

Insight into the bidirectional dynamics of hyperbolic tangent hybrid nanomaterial subject to Nield’s conditions using numerical approach

A hyperbolic tangent fluid model characterized by shear rate dependent viscosity together with the effects of hybrid nanoparticles, Brownian motion, thermo-diffusion, and Nield’s conditions, is utilized for thermal enhancement purpose. Five percent copper nanoparticles and twenty percent alumina nanoparticles are submerged into ethylene glycol with the parametric influence of tangent hyperbolic fluid to obtain the tangent hyperbolic hybrid nano suspension. Numerical solutions of the nondimensionalized conservation laws are found by the Keller-box method. The influence of various parametric factors on velocity, temperature, concentration, Nusselt number, and Sherwood number has been discussed. A constant Nusselt number is noted with the influence of Nield’s constraints. A 90% increase in thermal conductivity is achieved by dispersing 5% copper and 20% alumina nanoparticles into the ethylene glycol with the influence of hyperbolic tangent fluid. The error and convergence analysis of the numerical solution have been discussed, along with the validation of the obtained numerical results.

Novel Approach to Augment Thermal Conductivity of Dihybrid Nanofluids

In this experimental study, the copper oxide (CuO) nano–particle (NP) was mixed with a water/ethylene glycol hybrid base fluid to form a hybrid nano–fluid (HNF). Further, this HNF was mixed with a MgO nano–particle and also separately with a TiO2 nano–particle to form two different dihybrid nano–fluids (DHNFs). For the preparation of nano–fluids, two-step procedure was used. In all three cases, the volume fraction of the NP was 0.25, 0.5, 0.75, 1.0, and 1.25%. The thermal conductivity (TC) of HNF was measured with KD2 pro and compared with the DHNFs' at temperatures 26, 28, 30, and 32°C. It was inferred that the CuO/TiO2 nano–particle addition in the water/ethylene glycol hybrid base fluid resulted in an average of 0.8% rise in thermal conductivity at chosen temperatures and volume fraction. Also, the agglomeration due to the presence of CuO/MgO was a critical issue at higher volume fractions such as 0.75, 1, and 1.25%. The MgO nano–particle addition in the CuO nano–particle also resulted in a 0.6% increase in thermal conductivity at 0.25 and 0.5% volume fraction. The result was that in the CuO/MgO - water-ethylene glycol nano–fluid combination the TC was enhanced by 29.57% compared with CuO/water/ethylene glycol at a volume fraction increase of 0.5%. Also, it was noted that the nano–particles volume fraction has little effect on thermal conductivity improvement at higher proportion.

Performance of foam concrete developed from construction and demolition waste

Unconscious industrialization, urbanization and consumption of natural resources pose a serious threat to the environment. The threat can be reduced by upcycling construction and demolition waste (CDW) in the production of foam concrete, which is a special type of concrete used especially for thermal insulation purposes. This study aims to use of CDW as a source of fine aggregate (0–4 mm) in the production of foam concrete mixtures. A series of mixtures with target density values between 500 and 900 kg/m3 were designed with various recycled aggregate and foam contents to investigate the physical, mechanical and thermal properties of the mixtures. Findings of the study reveal that mixtures with an elevated foam content possess a greater number of larger pores, which, as observed through microscopy, form interconnected structures that are porous. On the other hand, adding more fine recycled material (FRM) makes the matrix denser, which reduces the overall porosity and increases the packing density. In contrast to increased content of FRM, correlation coefficient of (−0.77) reveal a more powerful inverse relationship between risen level of foam content (−0.67) and the reduction ratio of fresh-to-dry density and the increase in compressive strength from 7 to 28 days. It is also known that mixes with more foam have better thermal insulation because they trap more air, while mixes with more FRM show an increase in thermal conductivity. The sensitivity analysis showed that changes in thermal conductivity are almost three times as sensitive for FRM content, which means they have a bigger effect than changes in foam content. Employing the Taguchi method, (R_0.714) emerges as the most efficient tested combination indicative of superior overall performance. Notably, the Taguchi method predicts the untested combination (0.100-F/C ratio + 0.714-R/C ratio) as potentially more efficient, suggesting avenues for further exploration and optimization. This study furnishes valuable insights into sustainable construction practices by reutilizing CDW in foam concrete production, thereby contributing to both environmental conservation and enhanced structural outcomes.

Effect of Cu addition on the thermal conductivity and mechanical properties of Mg–Zn-xCu-Ce alloys

Thermal conductivity and mechanical properties of Mg–Zn-xCu-Ce alloys with different Cu contents under low extrusion temperature were systematically investigated in this work. The results shows that MgZnCu and Ce-rich (Mg, Zn, Cu, Ce) phase were formed in Mg–Zn-xCu-Ce alloys with high Cu content, which have significantly effect on the thermal conductivity and dynamic recrystallization (DRX). The distribution of grain morphology and LAGBs indicates that CDRX is the main mechanism. The addition of Cu element has an inhibitory effect on the DRX behavior, greatly refining the DRXed grains. After extrusion, a large amount of nano-phase is dispersed in the MZEC alloy, which has a strong pinning effect on dislocations. The formation of MgZnCu phase with high thermal conductivity sacrifices the solute atoms of Zn and Cu in α-Mg matrix, which leads to reduction of lattice distortion of Mg matrix, thereby ensuring high thermal conductivity of Mg–Zn–Cu–Ce ternary magnesium alloys. With the increase of Cu content, the strength and thermal conductivity of the alloy gradually increases. When the Cu content is 3.6 wt%, UTS (ultimate tensile strength), YS (yield strength), EL (elongation) and thermal conductivity are 350 MPa, 317 MPa,15.8% and 135 W/m∙K, respectively.

Enhanced thermal conductivity and mechanical property via improvement of hydrogen bonding between hexagonal boron nitride and aramid copolymer

This study focuses on enhancing thermal properties of aramid copolymer nanocomposites by integrating hexagonal boron nitride (hBN). Pristine hBN (P-hBN) is first subjected to oxidative heat treatment at 900 °C, producing thermally treated hBN (T-hBN), which significantly improves thermal conductivity while also increasing the tensile properties of composites. The study further explores the effect of different diamine co-monomers, 3,4′- and 4,4′-oxydianiline (ODA), on the nanocomposite properties. Both types of ODA-based composite films show improvement in various properties containing T-hBN. With 20 wt% of T-hBN, the 3,4′-ODA and 4,4′-ODA-based films exhibit 33.2 % and 290 % increase in tensile strength and thermal conductivity, respectively. The functionalization of hBN by heat treatment enhances the interaction between aramid copolymer and hBN and prevents the aggregation of hBN. The rough interface was shown in fractured images for films with T-hBN, suggesting that the composite films with T-hBN withstand higher external forces. In addition, it was observed that T-hBN exhibits better dispersion compared to P-hBN. This is supported by molecular dynamics (MD) simulation, and, in addition, it also provides the underlying mechanism for the property differences between both types of co-monomers.

Enhancements in thermal properties of binary alkali chloride salt by Al2O3 nanoparticles for thermal energy storage

The cost-effective molten chloride salts are promising heat transfer fluids for next-generation concentrating solar plants. However, their limited specific heat capacities and thermal conductivities hinder their applications. In this paper, molten salt-based nanofluids based on a binary chloride (50 mol.% NaCl, 50 mol.% KCl) with Al2O3 nanoparticles were proposed to enhance the thermal properties. Firstly, molecular dynamics simulations were employed to investigate the thermal properties of these nanofluids, focusing on various nanoparticle volume fractions within 1100∼1600 K. The findings reveal that as the nanoparticle fraction increases from 0% to 7%, the specific heat capacity and dynamic viscosity improve by≈14.9% and 34.8%–38.6%, respectively. Concurrently, the thermal conductivity increases by 10.0%–16.5%. Then, microstructure evolution was analyzed to elucidate the enhancing mechanism of the thermal conductivity. Specifically, the negatively charged nanoparticle surface selectively attracts Na+ and K+, resulting in the formation of a compressed layer around the nanoparticle where the short-range order of ions was intensified. As a result, the compressed layer serves as a thermal conduit between the Al2O3 nanoparticle and the surrounding salt, resulting in the enhancement of the thermal conductivity. Furthermore, additional analyses of thermal diffusion properties and energy density distributions provide indirect evidence for the existence of the compressed layer where ionic motion is restricted, further validating the enhancing mechanism.

A unified hybrid micromechanical model for predicting the thermal and electrical conductivity of graphene reinforced porous and saturated cement composites

Graphene fillers have gained widespread attention as functional reinforcements for cement composites due to their excellent physical properties. The prediction of the thermal and electrical properties of graphene reinforced cement composites (GRCCs) is of great importance for developing intelligent and multifunctional civil engineering materials and structures. In this current work, a unified hybrid micromechanical model combining effective medium theory (EMT) and Mori-Tanaka-Benveniste (MTB) is developed to simultaneously predict the thermal and electrical conductivity of the GRCCs with considering pores and saturation, in which mechanisms including phonon transport, electron tunnelling and Maxwell-Wagner-Sillars (MWS) polarization are incorporated. Graphene nanoplatelets (GNPs) reinforced cement composites (GNPRCCs) samples are prepared and tested to validate the developed unified model. The results show that the electrical conductivity of the GNPRCCs is more sensitive to saturation than the thermal conductivity. When the porosity n = 0.2 and the GNP concentration is 1 wt%, the relative thermal and electrical conductivity increases by 5 % and 193 %, respectively, when the saturation index increases from 0.6 to 1. Elongated pores are more favorable for the formation of ionic networks for electrical conductivity in the saturated GNPRCCs, while spherical pores are more beneficial for heat transport. Elongated graphene fillers are preferred for enhancing both the thermal and electrical conductivity of dry and saturated GNPRCCs. The work is envisaged to provide guidelines for developing multifunctional cement composites.

A novel candidate shape-stabilized phase change material for building energy conservation based on lauric acid/roasted iron tailings-expanded graphite

This study presents the fabrication of a novel shape-stabilized phase change material (SSPCM) characterized by high thermal capacity and heat transfer efficiency. The material was composed of lauric acid (LA) embedded in roasted iron tailings (RIT) and expanded graphite (EG), utilizing a straightforward, low-cost, and direct impregnation method. The as-prepared LA/RIT-EG SSPCM underwent a comprehensive analysis of leakage tests, surface morphology, chemical compatibility, phase change properties, thermal stability, and reliability. Furthermore, the heat transfer efficiency and thermal conductivity were measured through cooling tests and a laser thermal conductivity analyzer, respectively. The LA/RIT-EG formulation demonstrated an ability to absorb 61.57 wt% LA without leakage, maintaining excellent form-stability with a mass fraction proportion of 29:9.43 for RIT and EG. DSC results revealed phase temperatures and latent heats of 42.49–46.31 °C and 108.1–113.1 J/g, respectively. Compared to pure LA, LA/RIT-EG exhibited a 489.7 % increase in thermal conductivity. Additionally, heat storage and release rates were improved by 81.25 % and 88.24 %, respectively. The study elucidated the mechanism behind the enhancement in encapsulation capacity and thermal conductivity by RIT-EG, validated through specific surface area and wettability tests. Overall, the results suggest that LA/RIT-EG, characterized by high thermal capacity and heat transfer efficiency, holds promise as a potential candidate for thermal energy storage, particularly in the context of energy conservation in buildings.

On the Influence of Humidity on a Thermal Conductivity Sensor for the Detection of Hydrogen.

Thermal conductivity sensors face an omnipresent cross-influence through varying humidity levels in real-life applications. We present the results of investigations on the influence of humidity on a hydrogen thermal conductivity sensor and approaches for predicting the behavior of thermal conductivity towards humidity. A literature search and comparison of different mixing equations for binary gas mixtures were carried out. The theoretical results were compared with experimental results from three different thermal conductivity sensors with mixtures of water vapor in nitrogen. The mixing equations show a large discrepancy between each other. Some of the models predict a continuously decreasing thermal conductivity and some predict an increasing thermal conductivity for increasing levels of humidity. Our measurements indicate an increase in thermal conductivity followed by a decrease after reaching a peak value. It is shown that the measured behavior is reproducible with different sensors. Depending on the sensor, this corresponds to an error up to 2 vol.% in the measured hydrogen value. The measured behavior is consistent with only one of the three models. Compared to this model, our own sensor shows a maximum deviation of 1.4%. Mixing equations for gas mixtures must be chosen carefully, taking into consideration whether mixing partners include polar or non-polar molecules. Some simplified mixing equations cannot be used to calculate the thermal conductivity of water vapor in air or nitrogen.