Conductivity Enhancement Research Articles

Effectiveness of a PCM-based heat sink with partially filled metal foam for thermal management of electronics

Electronics often experience overheating, which occurs when insufficient or improper cooling causes temperatures to rise quickly, potentially leading to component failure. Recently, a passive technique utilizing phase change material (PCM)-based heat sinks is suitable for modern electronic cooling. However, due to its low thermal conductivity, Aluminum (Al) foam as a thermal conductivity enhancer (TCE) is used. In this study, a partial filling approach is employed, involving a heat sink designed to cool a protruding electronic component (EC) attached to a metal fin. The enthalpy-porosity method and the thermal equilibrium model are applied. Results show that the efficiency of the heat sink is improved by increasing the filling ratio of the Al foam, thereby reducing the EC temperature by 15.85 °C, shortness the melting time by more than 1000 s, and the overall effective conductivity enhanced by 25 times compared to the case without Al foam. In addition, the optimal partial filling ratio is determined to be 2/3, due to the considerable savings of 33.33 % in material cost and overall heat sink weight. The findings suggest that partial filling is a strategy that can be employed to achieve a more comprehensive performance in thermal management using PCM-based heat sinks.

Hydrogen-peroxide intercalated expanded graphite facilitates large enhancement in thermal conductivity of polyetherimide/graphite nanocomposites

In this work, we prepared expanded graphite (EG) filler using hydrogen peroxide (H2O2) as an oxidizing agent to study its impact on the thermal conductivity (k) of polyetherimide (PEI) composite, compared to EG prepared using sodium chlorate (NaClO3). Sulfuric acid was used as the primary intercalating agent for both synthesis routes. The use of H2O2 prepared EG (EG-H2O2) led to a remarkable ∼4030% enhancement (9.5 Wm−1K−1) in k of the PEI/EG composite, while the use of NaClO3 prepared EG (EG-NaClO3) led to a much smaller enhancement of ∼2190% (5.3 Wm−1K−1), at 10 wt% EG composition compared to kPEI (∼0.23 Wm−1K−1). Such findings exceed the current state-of-art in EG-based polymer composites. Detailed characterization was performed to understand the properties of EG-H2O2 and EG-NaClO3. Raman analysis revealed that H2O2 resulted in relatively defect-free EG (ID/IG ratio ∼0.04), thus preserving the k of graphite (∼2000 Wm−1K−1). Use of NaClO3, however, led to a large defect density (ID/IG ratio ∼0.25), yielding graphite with significantly diminished k. Furthermore, through-plane thermal diffusivity of EG-H2O2 paper was measured to be 9.5 mm2s-1 while that of NaClO3 case was measured to be 6.7 mm2s-1, thus directly confirming the beneficial impact of H2O2 in preserving the high k of graphene. X-ray photoelectron spectroscopy (XPS) revealed that the higher number of defects in EG-NaClO3 are due to the higher degree of oxidation induced by NaClO3. The results demonstrate the potential of EG-H₂O₂ as an efficient filler for achieving high thermal conductivity polymer composites.

Structural Landscape and Proton Conduction of Lanthanide 5-(Dihydroxyphosphoryl)isophthalates.

Metal phosphonate-carboxylate compounds represent a promising class of materials for proton conduction applications. This study investigates the structural, thermal, and proton conduction properties of three groups of lanthanide-based compounds derived from 5-(dihydroxyphosphoryl)isophthalic acid (PiPhtA). The crystal structures, solved ab initio from X-ray powder diffraction data, reveal that groups Ln-I, Ln[O3P-C6H3(COO)(COOH)(H2O)2] (Ln = La, Pr), and Ln-II, Ln2{[O3P-C6H3(COO)(COOH)]2(H2O)4}·2H2O (Ln = La, Pr, Eu), exhibit three-dimensional frameworks, while group Ln-III, Ln[O3P-C6H3(COO)(COOH)(H2O)] (Ln = Yb), adopts a layered structure with unbonded carboxylic groups oriented toward the interlayer region. All compounds feature carboxylic groups and coordinating water molecules. Impedance measurements demonstrate that these materials exhibit water-mediated proton conductivity, initially following a vehicle-type proton-transfer mechanism. Upon exposure to ammonia vapors from a 14 or 28% aqueous solution, compounds from groups II and III adsorb ammonia and water, leading to an enhancement in proton conductivity consistent with a Grotthuss-type proton-transfer mechanism. Notably, group II of the studied compounds undergoes the formation of a new expanded phase through the internal reaction of carboxylic groups with ammonia, coexisting with the as-synthesized phase. This postsynthetic modification results in a significant increase in proton conductivity, from approximately ∼5 × 10-6 to ∼10-4 S·cm-1 at 80 °C and 95% relative humidity (RH), attributed to a mixed intrinsic/extrinsic contribution. Remarkably, the NH3(28%)-exposed Yb-III compound achieves an enhancement in proton conductivity, reaching ∼ 5 × 10-3 S·cm-1 at 80 °C and 95% RH, primarily through an extrinsic contribution.

Boron Surface Treatment of Li7La3Zr2O12 Enabling Solid Composite Electrolytes for Li-metal Battery Applications.

Despite being promoted as a superior Li-ion conductor, lithium lanthanum zirconium oxide (LLZO) still suffers from a number of shortcomings when employed as an active ceramic filler in composite polymer-ceramic solid electrolytes for rechargeable all-solid-state lithium metal batteries. One of the main limitations is the detrimental presence of Li2CO3 on the surface of LLZO particles, restricting Li-ion transport at the polymer-ceramic interfaces. In this work, a facile way to improve this interface is presented, by purposely engineering the LLZO particle surfaces for better compatibility with a PEO:LiTFSI solid polymer electrolyte matrix. It is shown that an surface treatment based on immersing LLZO particles in a boric acid solution can improve the LLZO surface chemistry, resulting in an enhancement in the ionic conductivity and cation transference number of the CPE with 20 wt.% of boron-treated LLZO particles compared to the analogous CPE with non-treated LLZO. Ultimately, an improved cycling performance and stability in Li // LiFePO4 cells was also demonstrated for the modified material.

Simulation-Directed Construction of Bamboo-Forest-Like Heat Conduction Networks to Enhance Silicon Rubber Composites' Heat Conduction Properties.

Highly vertically thermally conductive silicon rubber (SiR) composites are widely used as thermal interface materials (TIMs) for chip cooling. Herein, inspired by water transport and transpiration of Moso bamboo-forests extensively existing in south China, and guided by filler self-assembly simulation, bamboo-forest-like heat conduction networks, with bamboo-stems-like vertically aligned polydopamine-coated carbon fibers (VA-PCFs), and bamboo-leaves-like horizontally layered Al2O3(HL-Al2O3), are rationally designed and constructed. VA-PCF/HL-Al2O3/SiR composites demonstrated enhanced heat conduction properties, and their through-plane thermal conductivity and thermal diffusivity reached 6.47W(mK)-1 and 3.98mm2s-1 at 12vol% PCF and 4vol% Al2O3 loadings, which are 32% and 38% higher than those of VA-PCF (12vol%) /SiR composites, respectively. The heat conduction enhancement mechanisms of VA-PCF/HL-Al2O3 networks on their SiR composites are revealed by multiscale simulation: HL-Al2O3 bridges the separate VA-PCF heat flow channels, and transfers more heat to the matrix, thereby increasing the vertical heat flux in composites. Along with high volume resistivity, low compression modulus, and coefficient of thermal expansion, VA-PCF/HL-Al2O3/SiR composites demonstrate great application potential as TIMs, which is proven using multiphysics simulation. This work not only makes a meaningful attempt at simulation-driven biomimetic material structure design but also provides inspiration for the preparation of TIMs.

Hygroscopic hydrogel-based cooling system for photovoltaic panels: An experimental and numerical study

Thermal management is an essential aspect of photovoltaic (PV) system design because of the negative effects of high temperatures on the efficiency of PV panels. The use of hygroscopic hydrogels for the evaporative cooling of PV panels is an emerging technique that has attracted attention owing to the high latent heat and recyclability of these materials. However, a comprehensive understanding of the heat and mass transport mechanisms in hygroscopic hydrogels is necessary. Factors that would ensure the long-term performance of PV panel/hydrogel (PV/HG) systems under real-world conditions are still poorly understood, and the intrinsic properties of hydrogels and the effect thereof on their cooling performance have hitherto remained unexplored. Herein, we propose a mathematical model for hydrogel-cooled PV panels to study the heat and mass transfer mechanisms of PV/HG systems in practical environments. The model is used to examine the impact of the thermal conductivity, diffusion coefficient, and thickness of the hydrogel on the performance of the PV/HG system. Unlike previously reported approaches to enhance the efficiency, in this study, the external heat transfer resistance and internal mass transfer resistance were identified as the primary controlling factors. Enhancement of the thermal conductivity of the hydrogel is shown to have a limited effect on the performance, whereas improving the water diffusion within the hydrogel significantly boosts the system efficiency. Optimally, the thickness of the hydrogel must be such that it balances the heat and mass transfer distances with the available water volume. During the summer in Guangzhou, China, a 6-mm thick layer of hydrogel lowered the temperature of a PV cell by up to 7.5 °C to increase the daily power generation by 2.1%. Analysis of the nationwide situation showed that hydrogels have substantial potential for lowering the peak PV panel temperatures (by as much as 19.3 °C) to mitigate fluctuations in the output power. Our findings offer valuable insights into the design of PV/HG systems towards improving their performance.

A model for zwitterionic polymers and their capacitance applications.

Zwitterions have been shown experimentally to enhance the dielectric constant of ionic media, owing to their large molecular dipole. Many studies since explored the enhancement of ionic conductivity with zwitterion additives as well as bulk behavior of zwitterions. Here, we examine the capacitance behavior of zwitterions between charged parallel plates using a mean-field theory. Employing only chain connectivity of a cation and anion with neutral monomers in between with mean-field electrostatics, we show that our model captures the high-dielectric behavior of zwitterions. We also predict an optimum in the capacitance of zwitterionic media as a function of chain length. To address the issue of zwitterion screening near charged surfaces, we demonstrate that zwitterions simultaneously partially screen charged walls and act as a pure dielectric that propagates the electric field far from the surface. Moreover, we show that salt solutions with zwitterionic additives outperform the energy density of both salt-only and zwitterion-only capacitors. We find that salt-only capacitors perform better at low applied potential, whereas salt capacitors with zwitterionic additives perform better at high applied potential.

Nature of electrically detected magnetic resonance in highly nitrogen-doped 6H -SiC single crystals

This work focuses on unraveling electron paramagnetic resonance (EPR) and electrically detected magnetic resonance (EDMR) properties of n-type 6H silicon carbide (SiC) single crystals with high concentrations of uncompensated nitrogen (N) donors, which is essential for fundamental understanding of spin-related phenomena, developing spin-based devices, optimizing materials and devices, and advancing research in quantum information and spintronics. Utilizing low-temperature multifrequency EPR spectroscopy (9.4–395.12 GHz), we identified two intense signals labeled as S line and S1 line in the 6H-SiC crystals with ND–NA≈8×1018 and 4×1019cm−3. In addition, in 6H-SiC crystals with ND–NA≈8×1018cm−3, a low-intensity triplet from N donors substituting the quasicubic “k2” nonequivalent position (Nk2) was observed. The S line [g⊥=2.0029(2),g∥=2.0038(2)] was assigned to the exchange interaction of conduction electrons and Nk2, while the S1 line [g⊥=2.0030(2),g∥=2.0040(2)] is caused by the exchange spin coupling of localized N donors at the “k1” and “k2” positions. The S1 line was observed in high-frequency EDMR spectra of 6H-SiC with ND–NA≈8×1018cm−3, and its emergence was explained by an enhancement of the hopping conductivity due to the EPR-induced temperature increase mechanism. No EDMR spectra were found to occur in the 6H-SiC crystals with ND–NA≈4×1019cm−3, which is close to the critical donor concentration value for a semiconductor-metal transition. Thus it can be concluded that this N donor concentration is too high for the appearance of spin-dependent scattering and too low for the emergence of EPR-induced hopping mechanisms in 6H-SiC. Published by the American Physical Society 2024

Investigation of the substitution of mercury by silver in Ag2S-HgS-GeS2 glasses: Macroscopic, electrical and vibrational properties

The evolution of structure and physical properties was investigated in the (Ag2S)x(HgS)50-x(GeS2)50 system. It was found that the density increases with increasing silver sulfide. The DSC data show a non-monotonic change of the glass transition temperature, Tg, from 243 °C (x = 0) to 301 °C (x = 50) with the minimum at 231 °C for x = 10 sample. The dual structure of HgS, which consists of the presence of dimorphic tetrahedral and chain forms of HgS, is found to be responsible for the non-monotonic change of the Tg. An increase in silver content leads to a significant enhancement of ionic conductivity from ∼10−14 S.cm−1 (x = 0) to ∼10−3 S.cm−1 (x = 50). The gradual structural evaluation is evidenced by the disappearance of the main Raman feature at ≈300 cm−1 related to the Hg-S stretching and the emergence of two contributions for silver-rich glasses at ≈370 cm−1 and at ≈400 cm−1.

Exploring electrochemical kinetic behaviors and interfacial charge transfer of pure and Ni-doped ZnFe2O4 nanoparticles-based sensing nanoplatform for ultra-sensitive detection of chloramphenicol

ZnFe2O4 (ZFO) nanomaterial was doped with a divalent transition metal cation of Ni2+ (NixZn1-xFe2O4, x=0, 0.2, 0.4, and 0.8) and characterized by various analytical techniques. Powder X-ray diffraction revealed the formation of a single-phase cubic spinel structure, while the stabilization of crystal structure for Ni2+-doped samples was observed. The average crystalline size, d-spacing, and lattice parameters increased with increasing in Ni2+ concentration within NixZn1-xFe2O4, due to differences in the ionic radius, the cation distribution at A-B sites, and the creation of surface oxygen vacancies within ZFO structure. From electrochemical measurements, NixZn1-xFe2O4-based electrodes showed excellent enhancements in charge transfer ability and conductivity with the highest rate constant (0.018 ms−1), the lowest peak-to-peak separation (206 mV), the lowest Rct (118 Ω), and the largest electrochemical active area (0.248 cm2), compared to that of bare SPE. Among them, Ni0.8Zn0.2Fe2O4/SPE provided outstanding electrochemical behaviors and achieved the best sensing performance with the widened concentration linear range from 0.25 to 50 μM and a rather low detection limit of 0.2 μM for chloramphenicol detection. The most important reason for this positive advance comes from the unique synergistic effects of Ni doping into the ZFO host structure. The excellent enhancements in adsorption capacity (Г) (1.4 times higher), number of oxygen vacancies, charge transfer rate constant (approximately 1.15 times higher), and catalytic rate constant (30 times greater) were recorded at Ni-doped ZFO-based electrodes, compared to pure ZFO-based electrode. Furthermore, the detailed hypotheses and possible mechanisms explaining these impressive enhancements were explored. Our work provides insight into the correlation between the Ni-doping and electrochemical characteristics, which has implications for tailoring the electrochemical performance of spinel ferrites across diverse applications and the design of novel spinel ferrite nanomaterials.

Free Volume Mediated Decoupling of Ionic Conduction from Segmental Relaxation Leading to Enhancement in Ionic Conductivity of Polymer Electrolytes at Low Temperatures.

Coupling between segmental relaxation and ionic conduction has limited the ionic conductivity of flexible polymers like poly(ethylene oxide), PEO, based electrolytes especially at low temperatures where segmental relaxation becomes extremely slow. In the present study, we show that ionic conduction becomes decoupled from segmental relaxation in PEO-based electrolytes simply by loading succinonitrile (SN). As a result of SN interactions induced rigid chain packing of PEO, the semicrystalline morphology of PEO is completely altered along with the enhancement in number density of free volumes having smaller size and narrower size distribution. These free volumes provide additional pathways for ionic diffusion independent of segmental relaxations of PEO leading to decoupling of ionic diffusion from the segmental relaxation process. The decoupling finally leads to nearly two orders higher ionic conductivity (∼10-11 Scm-1)at glass transition temperature (Tg ∼ 210 K), than what is expected in the case of complete coupling.

A disposable electrochemical sensor for amyloid-β42 protein based on molecular imprinted polymers with nitrogen doped carbon dots-graphene nanohybrid

This work presented a molecularly imprinted polymer (MIP) electrochemical sensor for determination of amyloid-β42 (Aβ42) as an Alzheimer’s disease (AD) biomarker. A nitrogen-doped carbon-dot-graphene (NCD-G) nanohybrid was synthesized through a simple ultrasonic method. Polypyrrole (PPY) was used as an imprinted polymer with an Aβ42 template for the electropolymerization process. The NCD-G and MIP were modified on a screen-printed carbon electrode (SPCE) without binding agent. The morphology and electrochemical properties of MIP/NCD-G modified SPCE were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV–Vis spectroscopy, X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV) and square wave voltammetry (SWV). The developed sensor exhibited good linear response in a range from 5 to 70 pg/mL with a limit of detection (LOD) of 1 pg/mL under optimal conditions. This sensor shows excellent performance due to the enhancement of effective surface area, electrical conductivity, and electrocatalytic activity. This MIP sensor takes advantage of molecularly imprinted technique combined with nanohybrid to achieve high selectivity and sensitivity. Moreover, it possessed good reproducibility and miniaturization that could be applied as a platform for portable devices in healthcare in the future. Novelty statementThis work provides the combination of a zero-dimensional and two-dimensional materials, nitrogen doped carbon dots-graphene nanohybrid (NCD-G) by self-assembly through a simple ultrasonication method and applied as a molecularly imprinted polymer (MIP) sensor for determination of amyloid-β42 protein. We propose a minimum number of preparation steps which NCD-G could enhance the MIP sensor performance, owing to the synergistic effects with high selectivity and sensitivity. The hybrid formation of the carbon dots with graphene using their π-π interactions in carbon nanostructures. NCD-G nanohybrid and MIP modified on screen printed carbon electrode (SPCE) for the determination of amyloid-β42 have not been previously investigated. Moreover, this disposable strip is a single-use tool that might be essential for on-site devices.

Optical, AC conductivity and antibacterial activity enhancement of chitosan-silver nanocomposites for optoelectronic and biomedical applications

This study is aimed to prepare and investigate the optical, electrical and antibacterial activity of the environmentally friendly (green) chitosan (Cs)/silver nanocomposites. TEM demonstrated that AgNPs have a spherical shape with particle size ranged from 3 nm to 25 nm. UV analysis spectra of Cs and Cs/Ag nanocomposites showed that, increasing the content of AgNPs led to a noticeable increase in the values of Urbach energy (E U ) and a dramatic decrease in both the indirect (E ig ) and direct (E dg ) optical bandgap energies. It is found that (E ig ) and (E dg ) are decreased from (4.72/5.31 eV) to (2.47/4.19 eV). The formation of the AgNPs is verified by the existence of surface plasmon resonance (SPR) peak at ∼ (421–450) nm. Wemple-DiDomenico and Sellmeier oscillator models are employed and displayed a clear enrichment in the dispersion energy (E d ) and oscillator energy (E 0) as well as the linear and nonlinear optical parameters of Cs. It is observed that the linear (χ(1)) and nonlinear (χ(3) and n2) parameters are enhanced from 0.083, 0.868 × 10−14 and 1.584 × 10−12 to 0.153, 9.762 × 10−14 and 4.088 × 10−12. The novel results in our study nominate Cs/Ag nanocomposites for applications in linear/nonlinear optical devices. AC conductivity behavior of Cs and Cs/Ag nanocomposites is analyzed based on Jonscher’s law and the analysis showed that the overlapping large polaron tunneling (OLPT) is the dominant conduction mechanism for our samples. It is clear that the values of dielectric constant (ε′) of Cs and Cs/Ag nanocomposites are higher confirming the presence of interface polarization (IP) relaxation. Moreover, it is found that the antibacterial activity of Cs against Gram-negative (P. aeruginosa) and Gram-positive (B. thuringiensis) bacteria is found to be enhanced with increasing the content of Ag NPs. These results suggested that Cs/Ag nanocomposites will be good source for preparing bio-nanocomposites for use in many biomedical and industrial applications.

Microstructure evolution and property enhancement of CuCr50 alloys through the synergistic effects by hot-forging deformation and heat treatment

In this study, CuCr50 alloys were prepared by aluminum thermal reduction-high frequency refining process, and the properties were improved through hot forging and heat treatment. With increasing deformation, large Cr particles were spheroidized and refined, significantly improving the performance of the alloy. When the deformation exceeds 27%, the conductivity reaches 17.73 MS/m, the hardness reaches 116.5 HB, and the density reaches 7.91 g/cm3. After solution at 975 °C for 1h and aging at 550 °C for 4h, the conductivity of the CuCr50 alloy further increased to 19.63 MS/m, the hardness reaches 121.5 HB. Compared with the as-cast alloy, the conductivity, hardness and density are increased by 71.07%, 18.81% and 2.99%, respectively. In the 5% deformed CuCr50 alloy the precipitates of nanoscale Cr particles formed a co-lattice with the copper matrix. In the 14% deformed CuCr50 alloy, nanoscale Cr particles precipitated and dispersed in the Cu matrix, and the relationship between the precipitated Cr phase and the Cu matrix was incoherent. The amount of precipitated Cr phase in the 27% deformed CuCr50 alloy had a semi-coherent relationship with the Cu matrix, the orientations of Cu(2‾00)//Cr(110). The hardness enhancement is mainly attributed to grain refinement and density increase, and the conductivity enhancement is mainly attributed to Cr particle precipitation after aging treatment.

Effects of mechanical alloying methods on structural phase stability, chemical state, optical, electrical and ferroelectric properties in Sc-doped α-Fe2O3 system

The development of metal doped α-Fe2O3 (hematite) based wide band gap semiconductors with high electrical conductivity, high electrical polarization and wide optical band gap is a challenging problem and also useful for application point of view. In this work, a substantial enhancement of electrical conductivity, optical band gap and ferroelectric polarization have been recorded at room temperature for Sc doped α-Fe2O3 system. Two different methods of the mechanical alloying and subsequent heat treatment have been used to synthesize the samples of α-Fe2-xScxO3 oxide (x = 0.2–1.0). The X-ray diffraction patterns have confirmed formation of single-phased Rhombohedral structure for low Sc doping content (x = 0.2), whereas a mixture of Rhombohedral-structured α-Fe2O3 type phase and cubic-structured Sc2O3 type phase has been formed for the higher Sc contents (x = 0.5 and 1.0). The phase fractions varied depending on the amount of Sc content, chemical reaction during mechanical alloying of the elementary oxides and solid-state reaction during the heat treatment. Response of the Sc2O3 type phase in Raman spectra is sensitive depending on the methods of inter-mixing the α-Fe2O3 and Sc2O3 by mechanical alloying. X-ray photoelectron spectroscopy (XPS) confirmed the metal (Fe, Sc) ions in +3 charge state, although the samples for low Sc content x = 0.2 showed a signature of Fe+2 and Sc+4 states. A detailed analysis of the Fe 3s XPS band confirmed a strong 3s-3d spins exchange coupling of strengths 1.18 eV–1.34 eV.

Plasticized PVC composites comprising MWCNT‐RGO hybrid filler–the synergetic effect of hybrids on the dielectric and mechanical properties

AbstractModification of polymers with hybrid fillers has sought much attention in the past few years. The addition of hybrid fillers will lead to a synergistic effect in reinforcing and is advantageous in polymer nanocomposites. One such attempt is presented here that explores the effect of incorporation of hybrid derived from reduced graphene oxide (RGO) and multiwalled carbon nanotubes (MWCNT) on the dielectric and mechanical properties of plasticized polyvinyl chloride (PPVC). This system of hybrid composite incorporating RGO‐CNT and PPVC has not been prepared and reported yet. Melt mixing techniques were effectively used for the fabrication of PPVC nanocomposites containing the hybrid filler in different ratios. The prepared composites showed enhanced dielectric strength in the lower frequency region up to 450 and high AC conductivity. The mutual stacking and penetration of the 1D‐2D nanomaterials lead to effective dispersion and enhancement in the electronic conduction. Among the hybrids, the R1C5 (with the filler ration RGO 1 wt% and CNT 5%) was having the optimum properties. The tensile modulus showed a cumulative variation with the addition of CNT. Even though the tensile strength decreased slightly because of the immobilization of the PPVC chains by the hybrid effect, the modulus value showed a marked increase of over 90% from the virgin polymer. The PPVC composite with R1C5 hybrid filler exhibited an EMI shielding efficiency of ⁓23 dB and it was frequency independent. The results suggest the composite R1C5 should be used as a cost‐effective material for applications in the L‐band and S‐band regions.

Casson hybrid nanofluid flow over a Riga plate for drug delivery applications with double diffusion

Abstract Casson fluid-mediated hybrid nanofluids are more effective at transferring heat than traditional heat transfer fluids in terms of thermal conductivity. Heat exchangers, cooling systems and other thermal management systems are ideal for use with Casson fluids. Precise control of the flow and release of medication is necessary when using Casson fluids in drug delivery systems because of their unique rheological properties. Nanotechnology involves the creation of nanoparticles that are loaded with drugs and distributed in Casson fluid-based carriers for targeted delivery. In this study, to create a hybrid nanofluid, both single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs) are dispersed in a Casson fluid with Fourier’s and Fick’s laws assumptions. The Casson fluid is suitable for various engineering and medical applications due to the enhancement of heat transfer and thermal conductivity by the carbon nanotubes. Our objective is to understand how SWCNTs and MWCNTs impact the flow field by studying the flow behavior of the Casson hybrid nanofluid when it is stretched against a Riga plate. The Darcy–Forchheimer model is also used to account for the impact of the porous medium near the stretching plate. Both linear and quadratic drag terms are taken into account in this model to accurately predict the flow behavior of the nanofluid. In addition, the homotopy analysis method is utilized to address the model problem. The outcomes are discussed and deliberated based on drug delivery applications. These findings shed valuable light on the flow characteristics of a Casson hybrid nanofluid comprising SWCNTs and MWCNTs. It is observed that the incorporation of carbon nanotubes makes the nanofluid a promising candidate for medical applications due to its improved heat transfer properties.

Synergistic Enhancement of Mechanical Properties and Electrical Conductivity of Immiscible Bimetal: A Case Study on W–Cu

Immiscible bimetal systems, of which tungsten–copper (W–Cu) is a typical representative, have crucial applications in fields requiring both mechanical and physical properties. Nevertheless, it is a major challenge to determine how to give full play to the advantages of the two phases of the bimetal and achieve outstanding comprehensive properties. In this study, an ultrafine-grained W–Cu bimetal with spatially connected Cu and specific W islands was fabricated through a designed powder-mixing process and subsequent rapid low-temperature sintering. The prepared bimetal concurrently has a high yield strength, large plastic strain, and high electrical conductivity. The stress distribution and strain response of individual phases in different types of W–Cu bimetals under loading were quantified by means of a simulation. The high yield strength of the reported bimetal results from the microstructure refinement and high contiguity of the grains in the W islands, which enhance the contribution of W to the total plastic deformation of the bimetal. The high electrical conductivity is attributed to the increased mean free path of the Cu and the reduced proportion of phase boundaries due to the specific phase combination of W islands and Cu. This work provides new insight into modulating phase configuration in immiscible metallic composites to achieve high-level multi-objective properties.

Passive battery thermal management and thermal safety protection based on hydrated salt composite phase change materials

Lithium-ion batteries (LIBs) are progressing towards higher energy densities, extended lifespans, and improved safety. However, battery thermal management systems are facing increased demand owing to high-rate charging and discharging, dynamic operating conditions, and heightened thermal safety concerns. Therefore, this paper proposes a novel composite phase change material (CPCM) comprising Na2SO4-10H2O as the core phase change material (PCM) and expanded graphite as the thermal conductivity enhancer. The CPCM offers high latent heat, superior thermal conductivity, and a two-stage temperature control function for battery thermal management and safety. The optimal mass CPCM ratio, determined through comprehensive characterization and thermal property tests, resulted in a melting point of 29.05°C, latent heat of 183.7 J.g−1, and high thermal conductivity of 3.926 W.m−1.K−1. During normal LIB operations, the CPCM efficiently absorbs and transfers heat, reducing the peak LIB temperature from 66 to 34°C at 15°C ambient temperature during a 3.7C high-rate discharge. Under dynamic conditions, the peak temperatures across the three cycles were consistently controlled at 36.7, 36.4, and 35.8°C, respectively. In a thermal runaway state, the thermochemical heat storage of hydrated salt dehydration effectively slowed LIB temperature increase, delaying the time to reach 130°C by 187 s. Suppression of the temperature rise outside the CPCM, combined with an extended dehydration plateau of up to 320 s, prevented the occurrence and propagation of thermal runaway in the battery.

Interfacial bonding mechanism of graphene nanoplatelets reinforced AZ91D magnesium alloy prepared by semi-solid injection molding

The incompatibility between the strength and thermal conductivity of magnesium alloys limits their application in heat dissipation components. Magnesium matrix composites were obtained by adding reinforcements into the AZ91D alloy to achieve synergistic enhancement of mechanical and thermal conductivity to promote the application of magnesium alloy. Graphene nanoplatelets (GNPs) reinforced magnesium matrix composites were successfully prepared by semi-solid injection molding. The high viscosity of the semi-solid metal slurry contributes to the homogeneous dispersion of GNPs in the magnesium matrix. A GNPs/MgO/Mg heterostructure with high interfacial bonding strength was found at the interface of GNPs and α-Mg matrix. The semi-solid casting method improves the mechanical properties of the composites by grain refinement and simultaneously reduces the thermal conductivity. The addition of GNPs can balance the mechanical and thermal conductivity enhancement, and the most balanced properties of the composites are obtained when the content of GNPs is 0.3 wt%, with a tensile strength of 243.1 MPa, Vickers hardness of 93.7 HV, and thermal conductivity of 74.8 W/(m·K). Therefore, the semi-solid forming method is considered a promising processing method, and GNPs is considered an ideal reinforcement material to improve the performance of the magnesium matrix.