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To date, the thermal and electrical properties of three‐phase ceramics containing a boride phase, silicon carbide, and boron carbide have not been studied in detail. Further, the effect of the source of the boride powder has also not been investigated. This study produced three‐phase ceramics containing titanium diboride, silicon carbide, and boron carbide using three different TiB2 sources: commercial powder, TiB2 synthesized by boro/carbothermal reduction, or (Ti,Cr)B2 synthesized by boro/carbothermal reduction to address the effect of the TiB2 source. Ceramics containing synthesized TiB2 or (Ti,Cr)B2 reached >99% relative density, while the ceramic produced from commercial powder reached ∼93% relative density. The addition of Cr reduced both the thermal and electrical conductivities, but had little effect on the Vickers hardness. The (Ti,Cr)B2–SiC–B4C ceramic had a thermal conductivity of ∼33 W/m K, an electrical conductivity of ∼105 S/m, and a hardness of ∼61 GPa at 0.49 N. The highest hardness of ∼66 GPa at a load of 0.49 N was for the TiB2–SiC–B4C ceramic made with synthesized TiB2 powder. [ABSTRACT FROM AUTHOR]

Glass foams and glass-ceramic foams exhibit great potential in thermal insulation of buildings, consequently reducing the necessity for heating or cooling, and ultimately contributing to energy saving. In this study, we prepared glass-ceramic foams utilizing silicate glass as starting material and CaCO 3 as foaming agent through a thermochemical process. Foams with varying degrees of relative crystallinity were produced by controlling temperature and duration of isothermal heat treatment. The foaming mechanism in the glass-ceramics was discussed by analyzing how the heat flow, mass, and volume evolve within the powder mixture during dynamic heating. The crystallization in glass did not show any clear trend on the compressive strength of glass foams. On the other hand, the thermal conductivity of the glass-ceramic foams increases with increasing relative crystallinity. The calculated solid thermal conductivity exhibited a minimum at low relative crystallinity (<20 %). These findings are crucial for designing high performance glass-ceramic foams for thermal insulation, potentially also for fabricating glass-ceramic foams using waste glasses. [ABSTRACT FROM AUTHOR]

Thermal protection was always a prominent issue in the aerospace industry. For vehicle safety, reliability and payload requirements, thermal protection materials were usually expected to possess low density, superior mechanical and thermal insulation properties. Here, lightweight and high-strength porous mullite-silica ceramics were manufactured using particle-stabilized foaming technique. The strength and thermal insulation properties of porous ceramics modified with hollow silica spheres were significantly enhanced. A 10 wt% hollow spheres addition achieved a 28.9 % increase in strength and a 33.4 % decrease in thermal conductivity with almost constant porosity (from 86.39 % to 87.04 %). Considering the characteristics of light weight, high compression strength and superior thermal insulation performance, porous ceramics could be applied as thermal protection materials in the aerospace sector. [ABSTRACT FROM AUTHOR]

Porous high-entropy transition metal compounds, an important type of ultra-high temperature material, have attracted increasing attention in the applications of extreme environments due to their low density, good thermal insulation and stable chemical properties. A robust, flame-retardant and high-temperature resistant high-entropy carbonitride (Ti 1/5 V 1/5 Mo 1/5 Nb 1/5 Ta 1/5)(C 0.55 N 0.45) (HECN) porous ceramic was synthesized and thoroughly characterized. It exhibited a porosity of 93.5 %, a compressive strength of 1.3 MPa and a good high-temperature stability up to 1673 K, which, along with its outstanding fire-retardancy, and low thermal conductivity (as low as 0.150 W m−1 K−1 at 298 K), made it a good candidate material for thermal insulation applications in ultra-high temperature environments. Moreover, the Density functional theory (DFT) calculations predict that the [N]/([C]+[N]) ratio in HECN foam affects its lattice thermal conductivity which is decreased by 67 % upon increasing the ratio from 0 to 1/2. [ABSTRACT FROM AUTHOR]

The preparation and characterization of composite materials composed of polypropylene (PP) as the base mixed with halloysite nanotubes (HNT) at various weight percentages (0.5, 1.5, and 3 wt.%) using a melt extrusion method operated at a temperature between 190 °C and 200 °C is described. The impact of the addition of the HNT filler on the PP nanocomposites was investigated based on the thermal and mechanical properties. The thermal characterization was conducted by differential scanning calorimetry (DSC). Significant increases in the rheological properties were observed with the addition of a high content of HNTs. The water absorption decreased with increasing HNT. The SEM micrographs showed that the HNT fillers were homogeneously dispersed throughout the entire PP matrix. [ABSTRACT FROM AUTHOR]

A sol-gel matrix was generated from S– and P-based acids to prepare a fire-retardant solution system for coating natural cotton fibers. The physical properties, surface morphology, and elemental composition of the coated samples were assessed using optical scanning electron microscopy. The thermal behavior of the coated samples was documented using TGA and VFT tests, which confirmed higher thermal stability of the phosphate-based coatings. High char residue formation (~44.5%) and self-extinguishing properties were observed for the phosphate-based coating under non-curing conditions. The superior properties of phosphate-based coatings P5-4h could be ascribed to the collaborative effect of P–Si–N—i.e., the combined activity during the combustion process and pyrolysis of the coated sample. [ABSTRACT FROM AUTHOR]

Mn6Ni16Si7 intermetallic compounds, referred to as the G phase, and their precursors are recognized as potential secondary phases precipitated in neutron-irradiated steels and are the main cause of embrittlement in low-alloyed reactor pressure vessel steels under long-term operation. To obtain the mechanical properties and thermal stability of the G phase, two Mn-Ni-Si model alloys (composed of 21 mol%Mn-58 mol%Ni-21 mol%Si and 30 mol%Mn-58 mol%Ni-12 mol%Si) were annealed at 1,000°C. The existence of the G phase in both annealed ternary model alloys was confirmed by XRD and SEM/EDS. Meanwhile, the process of different Mn-Ni-Si ternary regions to the G phase transformation under 1,000°C annealing has also been discussed. Young's modulus and nano-hardness of the G phase were measured using the nanoindentation technique. The results showed similar values for the G phase in two alloys with Young's modulus of approximately 220 GPa, which is similar to Young's modulus of iron. This fact suggests the necessity of reconsideration of the hardening model contributed by G phase precipitates in reactor pressure vessels in the future. [ABSTRACT FROM AUTHOR]

Investment casting is a widely utilized casting technique that offers superior dimensional accuracy and surface quality. In this method, the wax patterns are employed in the layer-by-layer formation of a shell mold. As is customary, the patterns were created through the injection of molten or semi-solid wax into the die. The quality of the final casting is affected by the quality of the wax pattern. Furthermore, the filling of the die with wax can be associated with die-filling challenges, such as the formation of weld lines and misruns. In this study, the injection filling of the fluidity probe die with RG20, S1235, and S1135 pattern waxes was simulated using ProCast software. The thermal properties of the waxes, including thermal conductivity, heat capacity, and density across a wide temperature range, were determined with the assistance of a laser flash analyzer, a differential scanning calorimeter, and a dynamic mechanical analyzer. A favorable comparison of the acquired properties with those reported in the literature was observed. The Carreau model, which corresponds to non-Newtonian flow, was employed, and the parameters in the Carreau viscosity equation were determined as functions of temperature. Utilizing the thermal data associated with the wax patterns and the simulation outcomes, the interfacial heat transfer coefficients between the wax and the die were ascertained, yielding a value of 275–475 W/m2K. A strong correlation was observed between the experimental and simulated filling percentages of the fluidity probe across a wide range of injection temperatures and pressures. The analysis of the simulated temperature, fraction solid, viscosity, and shear rate in the wax pattern revealed that viscosity is a crucial factor influencing the wax fluidity. It was demonstrated that waxes with an initial high viscosity exhibit a low shear rate, which subsequently increases the viscosity, thereby hindering the wax flow. [ABSTRACT FROM AUTHOR]

Thermoplastic polyimide (PI) matrixes, including PI-a (cc-34ODA) and PI-b (ct-34ODA) were prepared via the hot-pressing procedures of the resins derived from the 3,4′-oxydianiline (34ODA) and two alicyclic dianhydrides of 1S,2R,4S,5R-hydrogenated pyromellitic dianhydride (ccHPMDA) and 1R,2S,4S,5R-hydrogenated pyromellitic dianhydride (ctHPMDA), respectively. The resins exhibited thermoplastic features with good formability at higher temperatures. The afforded semi-alicyclic PI sheets exhibited enhanced properties in comparison to commercially available, wholly aromatic thermoplastic PIs, such as PI-ref1, which are derived from 3,3′,4,4′-oxydiphthalic anhydride (ODPA) and 4,4′-oxydianiline (44ODA), as well as PI-ref2, which is based on pyromellitic dianhydride (PMDA) and 4,4′-bis(3-aminophenoxy)biphenyl (mBAPB). In addition, the developed PI sheets exhibited high heat deflection temperatures (HDT) of 267.4 °C for PI-a and 268.6 °C for PI-b. There values were significantly higher when compared with those of PI-ref1 (Ratem® YS20, HDT: 239.0 °C), PI-ref2 (Aurum® PL450C, HDT: 238.0 °C), PI-ref3 (Ultem® 1000, HDT: 206.0 °C), PI-ref4 (Therplim® TO65, HDT: 180.0 °C), and PI-ref5 based on phthalic anhydride-terminated fluorinated PIs (HDT: 215.0 °C). In terms of mechanical properties, the current PI sheets showed superior flexural properties among the polymers with the flexural strength of 189.0 ± 11.7 MPa (PI-a) and 200.5 ± 4.2 MPa (PI-b), respectively. In addition, the PI sheets exhibited comparable compression properties, inferior impact strength, and tensile properties compared with the referenced PI counterparts. Basically, the PI-b sheet showed better comprehensive properties than those of the stereoisomeric PI-a analog. [ABSTRACT FROM AUTHOR]

In this work, composites made of polylactide (PLA) and filled with alkali-pretreated rice husk (RH) were investigated. Composites containing 20, 30, and 40 wt.% of RH were synthesized. It was shown that alkaline treatment, along with the change in crystal lattice, led to an increase in the content of non-crystalline parts and the volume of intercrystalline spaces, and the internal surface of the cellulose fiber increased, which resulted in improved adhesion of the fiber with the matrix. The addition of rice husk to the PLA matrix led to an increase in the flexural modulus, which increased to 2881 MPa for the PLA/RH (80/20 wt.%) and 3034 MPa for the PLA/RH (70/30 wt.%) composites and lowered the peak load stress by approximately 43% for the composite with 20 wt.% RH and 56% for the composite with 30 wt.% RH. The reduction in the degree of PLA crystallinity allows macromolecules to move more freely in amorphous regions, which has a positive effect on increasing the flexibility of materials in general. The optimal formulation is a composite consisting of 30% RH and 70% PLA matrix. [ABSTRACT FROM AUTHOR]

Polyoxymethylene (POM), polypropylene (PP), and poly(methyl methacrylate) (PMMA) have been blended with adhesive-grade ethylene vinyl acetate (EVA), propylene elastomer (VMX), isobutylene–isoprene rubber (IIR) and an acrylic block copolymer (MMA-nBA-MMA). The blends were prepared using a two-roll mill and injection molding. The mechanical properties of the blends, such as tensile strength, tensile modulus, elongation at maximum load, and impact resistance, were investigated. The water contact angle, melt flow rate (MFR), and differential scanning calorimetry were ascertained to evaluate the blends. The blend samples exhibited the following properties: all POM/EVA blends showed reduced crystallinity compared to neat POM; the 80% PMMA/20% MMA-nBA-MMA blend showed improved impact resistance by 243% compared to the neat PMMA. An antiplasticization effect was observed for POM/EVA 1% blends and PMMA/EVA 1% blends, with MFR reduced by 1% and 3%, respectively. The MFR of the PP/IIR 1% blend increased by 5%, then decreased below the MFR near the polymer for the remaining IIR concentrations. [ABSTRACT FROM AUTHOR]

In this work, 24CrNiMo alloy steel specimens were successfully prepared using laser direct metal deposition (LMD). The relationships between their microstructure, residual stress, as well as their thermal fatigue and wear properties for different types of treatments were then investigated. The treatments included quenching and tempering (QT), and stress relief annealing (SR) of the prepared samples. The study provided clear evidence that grain refinement was achieved after the QT and SR treatments. The hardness for the as-deposited specimens was found to be 325-380 HV0.2, while for the samples obtained after the QT and SR treatments, their values were obtained to be about 390 HV0.2 and 355 HV0.2, respectively. In comparison to the as-deposited samples, the QT treated specimens were reduced from a larger tensile stress of 176 ± 96 MPa to − 14 ± 5 MPa, while the SR specimens were reduced from 176 ± 96 MPa to − 44 ± 10 MPa. The microstructure and residual stress transformation resulted in improved wear resistance and thermal fatigue properties of the specimens, where the wear weights of the as-deposited specimens were about 13 and 3.7 times higher than that for the QT and SR processed specimens. Overall, a significant improvement in the mechanical properties of the QT treated specimens was achieved. [ABSTRACT FROM AUTHOR]

The increasing demand for high-performance materials has led to the development of natural fiber composites as an alternative to synthetic fiber composites. However, the low thermal conductivity of natural fibers limits their use in advanced applications. In this study, we have developed polyaniline-coated natural fiber composites to enhance their thermal properties. The methodology of this study involves the preparation of natural fiber composites using polyaniline-coated natural fibers as a reinforcement and a bio-based resin as a matrix. The composites were then coated with polyaniline, which was synthesized through chemical oxidation of aniline monomer. The coated composites were characterized using various analytical techniques such as Fourier-transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis to evaluate their structural, morphological, and thermal properties. The materials used in this study were natural fibers, bio-based resin, aniline monomer, ammonium persulfate, and hydrochloric acid. The gap identification of this study is the low thermal conductivity of natural fiber composites, which limits their application in advanced fields such as aerospace, automotive, and electronics. The problem identification is the lack of a cost-effective and eco-friendly method to enhance the thermal properties of natural fiber composites. The results of this study showed that the polyaniline-coated natural fiber composites exhibited enhanced thermal conductivity compared to the uncoated composites. The improvement in the properties of the composites was attributed to the high conductivity of polyaniline and its ability to form a continuous conductive network throughout the composite matrix. The development of polyaniline-coated natural fiber composites provides a cost-effective and eco-friendly approach to enhance the thermal properties of natural fiber composites. This approach has the potential to expand the use of natural fiber composites in advanced applications, leading to a sustainable and greener future. [ABSTRACT FROM AUTHOR]

This paper investigates the production of hydrothermal responsive shape memory filaments with different draw ratios (0.8, 2.0 and 3.2) using microcrystalline cellulose (MCC) as a filler and shape memory polyurethane (SMPU) as a matrix. A mechanical-thermo-aqueous programming test was conducted to study the shape-memory properties of the microcomposite filaments. The effect of draw ratio and triggering temperature on mechanical, physical, thermal, morphological, and shape memory properties was thoroughly studied. Among the microcomposite filaments, SMPU-MCC with a draw ratio of 2.0 exhibited the highest tenacity value of 0.91 cN/dtex in its original shape with an elongation of 385.2%. The differential scanning calorimetry results showed that the glass transition temperature (Tg) of the filaments increased as the draw ratio increased from 0.8 to 3.2, ranging from 38.35 to 41.02 °C. The crystallinity percentages obtained for pure SMPU, SMPU-MCC-0.8, SMPU-MCC-2.0, and SMPU-MCC-3.2 were 27.10%, 30.68%, 38.72%, and 36.88%, respectively. In addition, an optimum draw ratio led to a degradation temperature rise from 372.5 to 391.3 °C which shows the thermal stability of the filaments was significantly influenced by the intermolecular bonding between MCC and SMPU, which intensified as the draw ratio increased from 0.8 to 2.0. Moreover, the filaments exhibited excellent mechanical and thermal properties in six cycles at the optimum draw ratio and triggering temperature indicating their future application for repeated use without experiencing major changes in shape memory properties. [ABSTRACT FROM AUTHOR]

The hydrophilic property of lignocellulosic fibers is the main obstacle to improve the performance of structural bio-composites. To effectively utilize such fibers in high-performance composites, their hydrophobicity must be significantly increased. This study presents the hydrophobicity enhancement of okra woven fabric (OWF) by the application of hydrophobic nano-fumed silica (NFS) coating. Different concentrations of NFS were investigated, and SEM analysis confirmed that 1% NFS coated OWF presented the greatest quantity of nanoparticle deposition. The 1% NFS treated OWF exhibited the highest water contact angle of 137.2 ± 1° (~ 148% increased than uncoated fabric) and the greatest tensile strength of 21.85 ± 1.64 MPa in the warp direction and 15.66 ± 1.73 MPa in the weft direction (~ 46.35% and ~ 42.75% respectively superior to uncoated one). The TGA analysis demonstrated that the thermal characteristics have also been enhanced by NFS coating. The interaction between NFS and OWF has been investigated using FTIR analysis, while their elemental composition has been assessed using EDX and XPS techniques. [ABSTRACT FROM AUTHOR]

Balanced fertilizer application is crucial for achieving high-yield, high-quality, and efficient maize cultivation. Sulfur (S), considered a secondary nutrient, ranks as the fourth most essential plant nutrient after nitrogen (N), phosphorus (P), and potassium (K). S deficiency could significantly influence maize growth and development. Field experiments were conducted in Jiangsu, Yangzhou, China, from April 1 to July 20 in 2023. Jingkenuo2000 (JKN2000) and Suyunuo5 (SYN5) were used as experiment materials, and four treatments were set: no fertilizer application (F0), S fertilizer application (F1), conventional fertilization method (F2), and conventional fertilization method with additional S application (F3). The objective was to investigate the impact of S application on grain weight and the quality of fresh waxy maize flour and starch. The results indicated that all fertilization treatments significantly increased grain weight and the starch and protein contents in grains compared to no fertilization. Among these, F3 exhibited the most significant increases. Specifically, in JKN2000, the grain weight, starch content (SC), and protein content (PC) increased by 27.7%, 4.8%, and 14.8%, respectively, while in SYN5, these parameters increased by 26.3%, 6.2%, and 7.4%, respectively, followed by F2 and F1. Compared to F0, F3 increased starch and protein contents by 4.8% and 14.8% in JKN2000, and by 6.2% and 7.4% in SYN5. Compared to F0, F2 and F3 significantly increased the iodine binding capacity (IBC) of SYN5, with F3 being more effective than F2, while they had no significant effect on the IBC of JKN2000. The peak viscosity (PV) and breakdown viscosity (BD) of waxy maize flour and starch for both varieties showed a consistent response (increasing trend) to S application, and F3 had the largest increase. Regarding the thermal properties of waxy maize flour, F3 significantly enhanced the retrogradation enthalpy (ΔHgel) of both varieties compared to F0, while achieving the lowest retrogradation percentage (%R). In starch, the highest ΔHgel and the lowest %R were observed under the F2 treatment. In summary, under the conditions of this experiment, adding S fertilizer to conventional fertilization not only increased the grain weight of waxy maize but also effectively optimized the pasting and thermal properties of waxy maize flour and starch. [ABSTRACT FROM AUTHOR]

Furanoate polyesters are an extremely promising new class of materials for packaging applications, particularly furanoate-based nanocomposites, which have gained a high interest level in research and development in both academia and industries. The monomers utilised for the synthesis of furanoate-based polyesters were derived from lignocellulosic biomass, which is essential for both eco-friendliness and sustainability. Also, these polyesters have a lower carbon footprint compared to fossil-based plastics, contributing to greenhouse gas reduction. The furanoate-based nanocomposites exhibit enhanced performance characteristics, such as high thermal stability, excellent mechanical strength, superior barrier resistance, and good bacteriostatic rate, making them suitable for a wide range of industrial applications, especially for food-packaging applications. This paper reviews the recent trends in the synthesis routes of monomers, such as the various catalytic activities involved in the oxidation of 5(hydroxymethyl)furfural (HMF) into 2,5-furandicarboxylic acid (FDCA) and its ester, dimethyl furan-2,5-dicarboxylate (DMFD). In addition, this review explores the fabrication of different furanoate-based nanocomposites prepared by in situ polymerization, by melt mixing or solvent evaporation methods, and by using different types of nanoparticles to enhance the overall material properties of the resulting nanocomposites. Emphasis was given to presenting the effect of these nanoparticles on the furanoate polyester's properties. [ABSTRACT FROM AUTHOR]

The use of clays for thermal treatments and cosmetic purposes continues to be a worldwide practice, whether through the preservation of native cultural traditions, pharmaceutical formulations or integrative health and well-being practices. Special clays, such as bentonites, are very common for healing applications due to their high cation exchange capacity (CEC), high specific surface area (SSA) and alkaline pH values and, therefore, are used in multiple therapeutic and dermocosmetic treatments. Numerous bentonitic deposits occur on Porto Santo Island with different chemical weathering degrees. This research evaluates which residual soils have the most suitable characteristics for pelotherapy. The texture of residual soils varies from silt loam to loamy sand and SSA between 39 and 90 m2/g. The pH is alkaline (8.7 to 9.6), electrical conductivity ranges from 242 to 972 µS/cm, and CEC from 50.4 to 86.8 µS/cm. The residual soils have a siliciclastic composition (41.36 to 54.02% SiO2), between 12.52 and 17.65% Al2O3 and between 52 and 82% smectite content, which are montmorillonite and nontronite. Specific heat capacity (0.5–0.9 J/g°C) and cooling kinetics (14.5–19 min) show that one residual soil has the potential to be suitable for pelotherapy according to the literature. Moreover, the residual soils have As, Cd, Co, Cr, Hg, Mn, Ni, Pb, Sb and V concentrations higher than the limits of guidelines for cosmetics and pharmaceutical products. [ABSTRACT FROM AUTHOR]

In this study, the process parameters of fused filament fabrication are optimized to improve the tensile strength and impact energy of polylactic acid/carbon nanotube (PLA/CNT) composite. Hence, the utility function (UF) technique and response surface method (RSM) are applied to explore the optimal levels of the effective parameters of print speed, nozzle temperature, and CNT content. The differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and SEM analyses are employed to examine the thermal properties of the printed samples. The results of DSC and TGA analyses exhibited that the incorporation of CNT into PLA enhanced the thermal strength of PLA/CNT composite. The addition of CNTs in the composite improved the tensile strength by 37%, while the addition of CNTs up to 4 wt% improved the impact energy by 29%. Moreover, an increment of the print speed to 60 mm/s reduced the impact energy (12%) and tensile strength (22%), while an increment of the nozzle temperature to 200°C enhanced the impact energy (9%) and tensile strength (12%). The optimization results demonstrated that the strength and impact energy of PLA/CNT composite optimized at CNT content of 2.8 wt%, print speed of 20 mm/s, and nozzle temperature of 209°C. Additionally, the impact energy and tensile strength of the PLA/CNT composite enhanced up to 62.5 MPa and 2.14 J at the optimum conditions. Highlights: Application of FFF process for producing the PLA/CNT compositeInvestigating the impact of FFF parameters on the mechanical propertiesEstimating the optimal conditions of the FFF process [ABSTRACT FROM AUTHOR]

New foaming prepolymer compositions based on 4,4′‐oxydiphthalic anhydride, 4,4′‐diaminodiphenyl ether, 1,6‐hexamethylenediamine (HMDA), and a surfactant were synthesized. Polyimide (PI) foams containing from 0 to 40 mol% HMDA were prepared. The possibility of controlling the pore sizes in a foam material by selecting different fractions (250–400 μm) of particles of the powdered foam composition for heat treatment was shown. Scanning electron microscopy studies of morphology of the synthesized PI foams (PIFs) showed that all foams exhibited open cellular structures with pore diameters ranging from 50 to 500 μm. The influence of the components of the foaming composition (surfactant and aliphatic diamine) on the structure, thermal, and mechanical properties of the resulting PIFs was traced. The samples of PIFs containing 20% and 30% HMDA were elastic (the corresponding stress–strain curves were almost linear up to the 30% deformation) and able to restore their shape after removing the load. The resulting foams exhibited high thermal stability (the onset of weight loss was observed in the 470–500°C range). It was revealed that the synthesized PIF compositions were incombustible in an open flame. Due to their high heat resistance and nonflammability, the obtained PIFs can be used for thermal insulation applications in the aerospace, transport, construction, and microelectronics industries. Highlights: New, lightweight, flexible, and nonflammable PIFs have been synthesized.The HMDA additive imparts elasticity to PIFs.The introduction of a surfactant (KT‐6) makes the PIF homogeneous. [ABSTRACT FROM AUTHOR]

Light‐curing rapid prototyping (SLA) has become an emerging technology in the manufacturing industry because of its high precision, rapid prototyping, and the ability to mold complex parts. To enhance the mechanical properties and thermal stability of its raw material photosensitive resin (PR), carbon fiber (CF) was surface modified by chemical oxidation and grafting of amino silane (KH550) to obtain KH550‐modified carbon fiber (ACF). Then, ACF was composited with photosensitive resin to obtain modified carbon fiber/photosensitive resin (ACF/PR) composites. The viscosities of ACF/PR composites, including the viscosity, curing shrinkage, mechanical properties, and thermal stability of the ACF/PR composites, were characterized. The results showed that KH550 was successfully grafted onto CF. When the addition of ACF in the composites was 0.6%, the tensile strength, elongation at break, and impact strength of ACF/PR reached 39.48 MPa, 20.32%, and 13.62 kJ/m2, which were 120%, 27.15%, and 154% higher than that of the pure resin; the thermal decomposition temperatures and the maximum thermal decomposition temperatures at 50% mass loss of ACF/PR increased to 457.66°C and 442.44°C at 50% mass loss, which is 3.95% and 3.63% higher than that of the pure resin. Currently, the composites have excellent strength, toughness, and thermal stability. This paper gives a cost‐efficient method for improving the functioning of PR. Highlights: Mixed acid oxidation and amino silane modification of CFs.Preparation of modified CF/photosensitive resin composites.Composites with excellent mechanical properties and thermal stability. [ABSTRACT FROM AUTHOR]

The demand of natural fiber reinforced composites has grown enormously in polymer industries owing to their renewability and sustainability and maintaining their performance and properties. In this investigation, two natural fibers have been considered as a reinforcer to develop chemically functionalized high‐density polyethylene (CF‐HDPE)‐based composites. The total holocellulose content of ~85% and ~65% for nettle fiber (NTF) and oil palm empty fruit bunch fiber (OPF) make them significant for this study. OPF/CF‐HDPE and NTF/CF‐HDPE composites have been developed and characterized to measure their desirable properties. The structural confirmation suggests reinforcement/matrix adhesion through ester and hydrogen bonds between them. NTF/CF‐HDPE and OPF/CF‐HDPE are thermally stable upto 240°C and 250°C, respectively. A significant increment of ~40% and ~64% in tensile strength were observed in addition of OPF and NTF reinforcer in pristine matrix. A similar observation has been shown in flexural strength with improvement of ~58% and ~83% with OPF and NTF as reinforcer. Among all these composite compositions, the 30/70 NTF/CF‐HDPE composite demonstrated the highest tensile and flexural properties values due to higher holocellulose of NTF. This study demonstrates the potential of OPF and NTF reinforcer to develop natural fiber reinforced polymer composites, which helps respective industries to manufactured tailored made products with desirable properties. Highlights: OPF/CF‐HDPE and NTF/CF‐HDPE composites are sustainable and low cost.The composite compositions have been developed by extrusion and injection molding.The composite's mechanical (tensile and flexural) properties have been demonstrated.SEM and FTIR characterized the composites for the fiber/matrix adhesion.The composite's thermal stability has been affected by fibers and matrix. [ABSTRACT FROM AUTHOR]

The effect of different concentrations of fly ash aluminosilicate cenospheres on the structure and properties of elastomeric composites is studied. Composite materials based on ethylene–propylene–diene rubber (EPDM-40) with different mass fractions of fly ash (10, 20, 30%) are obtained using laboratory rollers. The microstructure of mixtures of EPDM and aluminosilicate cenospheres is studied by optical microscopy. It is shown that the concentration of the filler of more than 30 wt % increases the concentration of larger cenosphere agglomerates in the structure, which indicates interfacial separation in the mixtures, which is probably associated with the fact that mechanical mixing on mixing equipment does not make it possible to achieve uniform distribution of the filler throughout the elastomeric matrix. The appearance of new absorption bands in the region of 1400–800 cm–1 that correspond to the stretching vibrations of Si–O–Si present in aluminosilicate cenospheres is detected in the IR spectra. According to the thermogravimetry data of the compositions under study, the introduction of aluminosilicate cenospheres promotes a slight increase in the thermal stability of the composition under study with the concentration of cenospheres of more than 30%. The influence of the concentration of aluminosilicate cenospheres on the resistance of the composites to aggressive media is analyzed, and it is found that the introduction of a cenosphere filler in the amount of 10 to 30 wt % into mixtures based on EPDM can increase the oil and petrol resistance of the materials. [ABSTRACT FROM AUTHOR]

In this study, resveratrol was substituted for phenol in different molar ratios (4%, 8%, 12%, 16% and 20%) with lignin, phenol and formaldehyde as raw materials, and a new resveratrol modified lignin-based phenolic resin (R-LPF) with high glass transition temperature (Tg) and improved mechanical properties was synthesized. The curing behaviors of phenolic resin (PF), lignin phenolic resin (LPF) and R-LPF were investigated. The thermal mechanical properties, thermal stability, comprehensive mechanical properties, frictional properties and morphology were systematically tested and analyzed. The results show that the highest Tg of the modified R-LPF reaches 346.2 °C. The Ts reaches 231.5 °C, and the residual carbon rate reaches 66.2% at 800 °C. For 12% substitution ratio, the maximum tensile strength, bending strength and impact strength are respective 28.72 ± 1.10 MPa, 57.58 ± 1.95 MPa and 3.14 ± 0.19 KJ/m2. Compared with PF and LPF, the tensile strength of R-LPF is increased by 21.5% and 40.4%, and the bending strength is increased by 6.5% and 30.4%, while the impact strength is increased by 38.9% and 58.6%, respectively. The wear resistance is also significantly improved. The modified R-LPF structure has good rigidity, high crosslinking density, excellent mechanical and thermal properties, and it makes up for the defects of system performance decline caused by the introduction of lignin and provides a direction for the development of green high-performance phenolic resin. [ABSTRACT FROM AUTHOR]

The exceptional mechanical properties, dimensional stability and low cost of production of textile composites have made them quite popular in recent years. In the present analysis, plain woven inter, intra and hybrid carbon and E-glass fibre reinforced composites incorporated with or without nano-coconut shell ash (CSA) as filler were manufactured by hand lay-up method. The mechanical and thermal properties were determined for the manufactured composites. Simultaneously, the fractographic study was conducted by scanning electron microscopy to predict the different kind of failures in composites. The mechanical properties of the composites were found to be significantly better when 2 wt.% of CSA was substituted in it. The inter-hybrid composite containing 2 wt.% nanofiller demonstrated the highest tensile strength of 245.96 MPa, flexural strength of 496.03 MPa and maximum degradation temperature with weight change of 81.08%. A combination of intra- and inter-hybrid woven composite revealed the highest impact resistance of 3.3 J. The pseudo-ductile performance of intra-hybrid composites is also distinctly observed, showing moderate tensile stress of 299.376 MPa and maximum elongation of 5.137 mm. The current scientific effort makes it clear that the greatest tensile strength was obtained by positioning carbon fibres inside and the glass fibres outside. The surface proximity and diffusion of nanofillers in the composites further enhanced their tensile properties. Shear dispersion also led to maximum energy absorption without the need for nanofiller in case of combination of intra- and inter-woven fibre composites. [ABSTRACT FROM AUTHOR]

Natural fibers and nanomaterials are currently receiving more attention in the construction sector for two reasons. One reason is to use natural fibers instead of synthetic ones in fiber-reinforced concrete to create environmentally friendly products. In this study, sisal fiber (SF) and Cloisite 30B nanoclay particles were used to manufacture cement nano concrete. The cement nano concrete was reinforced with 3 wt% 10 mm sisal fiber and varying levels of Cloisite 30B nanoclay (0%, 0.5%, 1%, 1.5%, and 2%). Comprehensive research was conducted to evaluate the physical, mechanical, thermal, and water absorption properties of the concrete. The results indicate that the incorporation of nanoclay enhances these qualities. The results of the experiments indicated above demonstrate that the 3 wt% SF and 1.5% nanoclay concrete has superior mechanical qualities to other nanoclay concrete in terms of compressive strength (7.12 MPa) and flexural strength (9.6 MPa). Additionally, testing was performed on the concrete's morphology, physical properties, and water absorption. [ABSTRACT FROM AUTHOR]

This work aims to convert the bio-waste material into a fruitful product. This prepared product can be a solution for environmentally hazardous materials like polymer bags and plastic food wrappers. The prepared material is composed of bio-waste pomegranate peel powder and environmentally friendly polyvinyl alcohol. To extend its functionality in food wrappers, the silver nitrate solution is incorporated. The prepared samples were undergone various performance studies. The prepared films show high thermal with standing capacity and tensile properties and especially show better results in biodegradability as well as antibacterial activity. Among the fabricated films, the 5 mM AgNO3-fabricated film shows that the thermal stability up to 331 °C also possesses higher tensile strength of 25.7 MPa. These results make the possibilities of the fabricated PP/PVA/5 mM AgNPs film as an alternative for conventionally used plastic-based food wrappers. [ABSTRACT FROM AUTHOR]

More than 50% of the flame retardants used in the polymer and plastic industries are metal hydroxides. Among them, aluminum trihydroxide (ATH) is the most widely used due to its low toxicity and corrosiveness and its cost-effectiveness. The use of high-volume ATH in polymers reduces the mechanical properties. In this work, clay nanoparticles were added into epoxy/glass fiber/ATH hybrid composites to improve the mechanical and thermal properties of the composites. The effect of nano-clay content (1, 3, and 5 phr) on mechanical properties such as tensile and flexural strength and modulus, and thermal properties was investigated. Thermal properties were evaluated by Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA). The result of mechanical tests showed that adding 3 phr of clay nanoparticles increases tensile and flexural strength by 10% and 9.2%, respectively. The flammability of the composites was measured in horizontal mode. The flammability results revealed that introducing 3 phr of nano-clay improves the flammability of the composites by 41%. [ABSTRACT FROM AUTHOR]

BACKGROUND RESULTS CONCLUSION Starch from a non‐conventional source such as cardaba banana is relatively underexplored compared to conventional sources such as potato, maize or tapioca. Its high amylose content, however, suggests its suitability for specific industrial uses. Understanding the flowability, rheology and thermal properties of cardaba banana starch could lead to its novel application in food product formulation and pharmaceutical industry. Therefore, the present study aimed to examine the effect of modification on the bulk material characterization (powder flowability), granule size and shape (measured by light microscope), rheology and thermal properties of cardaba banana starch.The flowability of cross‐linked starch was affected significantly by the granule size (105 892.7 μm), shape (circularity 0.78) and compressibility (0.20), making it a more free‐flowing powder than other starch powders. The rheological behavior of the starch paste revealed that the Herschel–Bulkley model best predicts the rheological behavior with the highest coefficient of determinant (R2 > 0.9).Cross‐linked Cardaba banana starch with an excellent characteristic will find good application in food products that require free‐flowing behavior. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Highlights The impact of carbon fiber (CF) composites sizing with graphene oxide (GO) to form brick‐and‐mortar structures on their mechanical properties and thermal conductivity has not been closely examined. This study systematically investigates the effect of GO sheet size on the interfacial properties and thermal conductivity of CF composites. Three sizes of GO—small (0.11 μm), medium (0.33 μm), and large (0.97 μm)—were used to modify CF surfaces via layer‐by‐layer self‐assembly, forming the brick‐and‐mortar structures. The mechanical properties were assessed through flexural tests, interlaminar shear strength (ILSS) tests and tensile tests, while thermal conductivity was measured using a thermal constant analyzer. The results revealed that medium‐sized GO (GO‐M) significantly enhanced the interfacial strength and toughness of the composites. This improvement is attributed to the orderly arrangement of GO‐M on the CF surface, which enhances stress transfer between the fiber and the matrix. In contrast, small‐sized GO (GO‐S) tended to scatter, resulting in less effective reinforcement, while large‐sized GO (GO‐L) exhibited stacking and agglomeration, limiting its reinforcement effectiveness. However, GO‐L provided the highest thermal conductivity due to the formation of continuous heat conduction pathways. These findings suggest that GO‐M offers a balanced improvement in mechanical properties, whereas GO‐L is more suitable for applications requiring high thermal conductivity. This work underscores the importance of selecting the appropriate GO sheet size to optimize the interfacial properties and thermal conductivity of CF composites, which is crucial for enhancing their performance in high‐end engineering applications, such as aerospace, automotive, and marine industries. Modification of CF composites by GO‐M sheets significantly improved toughness and strength. GO‐L sheets formed an effective heat transfer channel with the highest thermal conductivity. The study emphasized the critical role of selecting the appropriate GO sheet size to optimize the mechanical and thermal properties of CF composites. [ABSTRACT FROM AUTHOR]

Diamond is a potential host material for laser applications due to its exceptional thermal properties, ultrawide bandgap, and color centers, which promise gain across the visible spectrum. More recently, coherent laser methods offer improved sensitivity for magnetometry. However, diamond fabrication is difficult in comparison to other crystalline matrices, and many optical loss channels are not yet understood. Here, we demonstrate a continuous-wave laser threshold as a function of the pump intensity on nitrogen-vacancy (NV) color centers. To achieve this, we constructed a laser cavity with both an NV diamond medium and an intracavity antireflection-coated diode laser. This dual-medium approach compensates intrinsic losses of the cavity by providing a fixed additional gain below threshold of the diode laser. We observe a continuous-wave laser threshold of the laser system and linewidth narrowing with increasing green pump power on the NV centers. Our results are a major development toward coherent approaches to magnetometry. [ABSTRACT FROM AUTHOR]

AbstractThe donor-acceptor (D-A) strategy has proven to be one of the most effective methods for tuning the band gaps, absorption characteristics, and optoelectronic properties in conjugated polymers. Two novel D-A conjugated polymers, PDBSTPD-1T and PDBSTPD-2T, were synthesized using dibenzosilole (DBS) and thieno[3,4-c]pyrrole-4,6-dione (TPD) as the building blocks. These polymers were linked through either a single thiophene or two thiophene rings as π-bridges and were copolymerized using a Suzuki coupling reaction. The effect of the incorporation of the different π-bridges on the electrical/optical properties of the prepared copolymers was also investigated. The synthesized polymers, PDBSTPD-1T and PDBSTPD-2T, were soluble in organic solvents and demonstrated high molar mass along with excellent thermal stability. The conjugation of the electron-accepting TPD unit with the electron-donating DBS unit produced relatively deep HOMO levels, which were fine-tuned to be −5.44 and −5.36 eV via the addition of the different π-bridges. PDBSTPD-1T and PDBSTPD-2T displayed absorption wavelengths between 350 and 650 nm with high Egopt of 2.01 and 1.97 eV, respectively. X-ray diffraction analysis presented several diffraction peaks, and the π-π stacking distances of PDBSTPD-1T and PDBSTPD-2T were 3.45 and 3.65°A, respectively. [ABSTRACT FROM AUTHOR]

Diurnal and seasonal variations in soil and surface temperature measured with the HP3 ${\mathrm{H}\mathrm{P}}^{3}$ thermal probe and radiometer of NASA's InSight Mars mission are reported. At a representative depth of 10–20 cm, an average temperature of 217.5 K was found, varying by 5.3–6.7 K during a sol and by 13.3 K during the seasons. From the damping of the temperature variation with depth and the phase shift, a thermal diffusivity of (3.93 ± $\pm $ 0.39) × 10−8 ${10}^{-8}$m2 ${\mathrm{m}}^{2}$/s was derived for the upper ∼ ${\sim} $10 cm from the diurnal temperature variation and of (3.63 ± $\pm $ 0.53) × 10−8 ${10}^{-8}$m2 ${\mathrm{m}}^{2}$/s for the ∼ ${\sim} $40 cm depth range of the mole from the annual temperature variation. Using published thermal conductivity and inertia values together with the diffusivities, soil densities of 1,470 and 1,730 kg/m3 ${m}^{3}$ were derived for these depths. The temperatures allow the deliquescence of thin films of brine, the efflorescence of which may explain the cemented duricrust observed. Plain Language Summary: Temperature is an important factor in understanding the physical properties of Martian soil. It determines how quickly physical processes and chemical reactions occur, including the transport of heat and materials. Temperature is crucial to astrobiology because it affects the habitability of the soil and the potential for water or brine to support microbial life. We measured the temperature in the soil during several Martian days and over a Martian year using the NASA InSight Mars mission's Heat Flow and Physical Properties Package. The average temperature was −56°C (217.5 K) over the depth extent of the thermal probe, which was about 40 cm. The temperature varied by 5–7° during the day, which is only a tenth of the daily surface temperature variation. It varied by 13° during the seasons. The temperature is subfreezing for water, but it allows the formation of thin films of salty brine for 10 hr or more during a Martian day. The solidification of the brine is a likely explanation for the observed few tens of centimeters thick duricrust, a layer of consolidated, cohesive sand, which is thought to have hampered the penetration to greater depth of the mission's thermal probe. Key Points: We measured the temperature and its diurnal and annual variations in the top 40 cm of the Martian soil at the InSight landing siteThe soil thermal diffusivity was calculated from the diurnal and seasonal surface and soil temperature variationsThe soil temperature allows the formation of thin films of brine; their efflorescence may explain the formation of the observed duricrust [ABSTRACT FROM AUTHOR]

This study investigates the practical applications of biochar as an innovative and sustainable conductive filler in composite materials. Utilizing the conventional melt-blending method, we prepared conductive pinewood biochar-filled poly(lactic acid)/poly(butylene adipate-co-terephthalate) (PLA/PBAT) composites and systematically examined their electrical, mechanical, rheological and thermal properties. Our results reveal a significant enhancement of electrical and mechanical properties upon the inclusion of conductive pinewood biochar in the PLA/PBAT matrix. With the addition of 10 wt% of conductive pinewood biochar, the average surface resistivity of the composites decreased by three orders of magnitude, measuring $4.86 \times {10^{10}}{\rm{\Omega }}/{\rm{sq}}$4.86×1010Ω/sq, which meets the antistatic requirements for polymer composites. Additionally, the average tensile strength of the biochar filler composites improved by 53% with an addition of just 1 wt% of biochar. [ABSTRACT FROM AUTHOR]

Rare‐earth hafnates are gaining attention due to their excellent high‐temperature phase stability and low thermal conductivity. However, they still have shortcomings of low thermal expansion and poor calcium‐magnesium‐aluminum‐silicate (CMAS) corrosion resistance. In this study, we employed high‐entropy engineering and component design to synthesize three high‐entropy hafnates (La0.2Ce0.2Nd0.2Gd0.2T0.2)2Hf2O7 (T = Dy, Ho, Tm) as well as a single‐component hafnate Nd2Hf2O7, with the aim of preparing thermal barrier coatings with an excellent comprehensive performance. Test results indicate that the high‐entropy compositions have excellent thermal properties. The focus is on elucidating the corrosion process and failure mechanism of CMAS at 1300°C. Moreover, the analysis of residual CMAS and corrosion products was conducted to evaluate the discrepancies in CMAS corrosion behavior among the various compositions. [ABSTRACT FROM AUTHOR]

In this research study, the synthesis of poly lactic acid (PLA) based bio composite material factors contributions were investigated through the Taguchi-based grey relational analysis (GRA) technique. Effects of micro crystalline cellulose (MCC) and montmorillonite (MTT) nano clay filler, sorbitol (S) plasticizer, and temperature (T) operating factor on the PLA matrix through melt-mixing preparation method. The tensile strength (TS), Young modulus (YM), flexural strength (FS), flexural modulus (FM), hardness, impact strength (IS), water absorption (WA), and density properties of bio composite material were investigated for each experimental setup (orthogonal array, L16). Additionally, neat PLA and optimal sample structural, thermal, and morphological properties were examined through Fourier transform infrared spectroscopy (FTIR), X-Ray diffraction (X-RD), thermal gravimetry analysis/differential thermal gravimetry (TGA/DTG), and DSC and SEM analyses. The obtained result for optimal mechanical and physical properties of MCC/MTT/S/PLA bio composite was MCC at level 3 (6%), MTT at level 4 (9%), S at level 2 (10%), and T at level 4 (175 °C). Analysis of variance (ANOVA) shows that MTT has the greatest significant effect on mechanical and physical properties of MCC/MTT/S/PLA bio composite followed by MCC, T, and S. The confirmation test indicates that the improvement of weighted grey relational grade (GRG) from 0.7896 to 0.846 and the FTIR, XRD, thermal gravimetry/differential scanning calorimetry (TG/DSC), and scanning electron microscopy (SEM) results indicates that the good interaction between PLA and fillers, improvement of thermal and morphological properties of optimal (6MCC/9MTT/10S/175 °C) bio composite samples. Therefore, the multi-response characteristics of MCC/MTT/S/PLA bio composite can be highly improved by this technique. [ABSTRACT FROM AUTHOR]

Ultra‐wide bandgap semiconductor AlGaN is a promising candidate for high‐power and high‐frequency electronics. AlGaN‐heterostructures with nitrogen (N)‐polarity can offer added benefits of low‐leakage and large drive current. However, electro‐thermal transport in such heterostructures remains unexplored, although they are essential for electronic device functionality. Here, the thermal and electrical properties of N‐polar AlxGa1‐xN‐channel heterostructures (Al percentage, x = 15–90%) are explored and compared with their GaN counterpart. The thermal measurements uncover that the effective thermal resistance of the thin channel and barrier layers are similar in magnitudes for N‐polar‐ AlGaN and GaN heterostructures, however, the total effective thermal conductivity in N‐polar AlGaN heterostructure is ≈4× smaller. This reduction originates from the larger thermal resistance of the thick Al0.15Ga0.85N buffer layer within the AlGaN stack. N‐polar AlxGa1‐xN stack displays a thermal conductivity almost independent of temperature, measured from room temperature up to 200 °C. Hall measurements of an N‐polar Al0.30Ga0.70N‐channel heterostructure further reveal that electrical properties such as resistivity, carrier density, and mobility remain nearly unchanged with temperature, indicating the dominance of alloy‐phonon scattering in such material systems. These results offer important insights into material‐device co‐design and reliability of N‐polar AlGaN heterostructures. [ABSTRACT FROM AUTHOR]

Bio‐based materials as crosslinkers for composites have gained attention for their nontoxic, cost‐effective benefits. Using eco‐friendly crosslinkers enhances the properties of the composites and promotes sustainable manufacturing practices too. This study aimed to compare the efficacy of citric acid (CA), itaconic acid (IA), and tannic acid (TA), derived from plant‐based sources, as crosslinkers in the creation of green composites. In this work, compression molding technique was employed for producing composites using coconut fiber as the reinforcing agent and methacrylic anhydride modified epoxidized linseed soybean oil (MAELSO) as the resin. The amount of crosslinkers was varied between 5, 10, and 15 (wt%) to achieve this. Nuclear magnetic resonance spectroscopy confirmed the successful modification of the resin. Fourier transform infrared spectroscopy revealed interactions between components of the composites. Biocomposites loaded with 5 wt% of CA showed 1268 and 92% increase in tensile strength and 1098 and 49% increase in flexural strength compared to those of similar wt% of TA‐ and IA‐based composites respectively. Similarly, the impact strength for CA‐based composite was 84.94 J/m against 168.74 J/m for IA and 330.85 J/m for TA‐based composites. Additionally, composites containing 5 wt% CA exhibited the highest levels of chemical resistance, flame retardancy, and thermal stability. Thus the results suggest that citric acid can serve as an effective crosslinker to fabricate environmentally acceptable composite materials that are suitable for long‐term use. This is noteworthy as it can pave the way for the production of sustainable and eco‐friendly materials, which can be used in various industrial and commercial applications. [ABSTRACT FROM AUTHOR]

Highlights Carbon black (CB) with different structural parameters together with graphene oxide were formed into uniformly dispersed filler network for enhancing the abrasion resistance of natural rubber/cis‐1,4‐polybutadiene rubber/trans‐1,4‐poly(isoprene‐butadiene) rubber blended composites. It showed that the CB structural parameters, such as specific surface area, surface activity and structural degree affected the formation of bound rubber. With the increase of bound rubber content, the homogeneity of filler network structure was improved and the filler‐rubber interaction was enhanced, resulting in a remarkable increase in the mechanical properties, thermal performance and abrasion resistance of the composites. Among the different types of CB, the composites filled with high‐structural‐degree CB of N134 had DIN wear volume as low as 76 mm3 and exhibited 19.5% higher abrasion resistance than N330. Wear surface observations and wear mechanism analyses showed that the increase in abrasion resistance was related to the improvement in tear resistance, hardness and thermal properties of the composites. Multiple linear regression analyses yielded that the structural degree in the structural parameters of CB had a significant correlation effect on the formation of bound rubber, and there was a strong linear relationship between the abrasion resistance of the composites and the content of bound rubber. Trans‐1,4‐poly(isoprene‐butadiene) rubber as compatibilizer for NR/BR blends. Synergistic enhancement of rubber using carbon black and graphene oxide. Carbon black with high structural degree promotes the formation of bound rubber. Described correlation between CB structural parameters and abrasion resistance of rubber. [ABSTRACT FROM AUTHOR]

Highlights Microfibrillated cellulose (MFC) was uniformly dispersed in high‐density polyethylene (HDPE) using a large amount of surfactant, and composites were prepared after removing the surfactant at different contents. The structural, morphological, thermal, and tensile properties of these composites were systematically investigated. The results demonstrated an asymptotic relationship between the amount of surfactant removed and the number of removal cycles. A negative linear correlation was observed between the surfactant content and the tensile strength, tensile modulus, and storage modulus at −20 °C of the composites, while a positive linear correlation was found with the loss modulus at −20 °C. Excessive surfactant adversely affected the dispersion of MFC, as well as the mechanical properties and thermal stability of the composites. However, when the surfactant content was below 2.8%, its impact on the composite properties was minimal, and the tensile strength, modulus, and thermal stability of the composites were significantly improved compared to neat HDPE. These findings indicate that surfactant pretreatment is an effective strategy for dispersing MFC in non‐polar polymers, and controlling the surfactant content in the final product can effectively tailor the properties of the resulting composites. Confirms the relationship between surfactant content and MFC/HDPE composite properties. Surfactant content showed an asymptotic relationship with removal cycles. Surfactant content and mechanical properties exhibited a negative linear correlation. Surfactant content and thermal stability exhibited a negative relationship. Surfactant content had minor impact when below 2.8%. [ABSTRACT FROM AUTHOR]

Comprehensive Summary Post‐polymerization modification provides an important approach to tuning the material properties of obtained polymers. In this work, we demonstrated a rational design of novel vinylcyclopropane monomer bearing a pendant N‐hydroxylphthalimide redox ester, and explored its radical ring‐opening polymerization behavior under visible‐light conditions. Photochemical decarboxylation of resulted polymer provided unique access to poly(vinylcyclopropane) bearing single ester group in each repeating unit. This decarboxylative modification has greatly reshaped the thermal and mechanical properties, converting a glassy polymer into a soft, ductile, and rubber‐like material. [ABSTRACT FROM AUTHOR]

Amino acid‐based poly(ester urea)s are an attractive class of polymers that are of interest for a variety of biomedical applications. Generally, amino acid‐based poly(ester urea)s are prepared by polymerization of diamines, which are obtained from the corresponding amino acids and aliphatic diols. This article presents an alternative synthetic strategy that uses diamine monomers obtained from aromatic, 4‐hydroxycinnamic acid‐derived diols. A library of structurally related diamine monomers has been prepared by coupling l‐leucine to 4‐hydroxycinnamic acid‐based diols that incorporate alkyl spacers of different lengths. The exploration of 4‐hydroxycinnamic acid as a building block is interesting as it can be obtained from various biological resources, such as for example lignin, and thus provides an opportunity to take advantage of (under‐utilized) bio‐based renewables for the design of new polymer materials. These diamine monomers can be copolymerized in a solvent‐free, one‐pot, two‐step process using dimethyl carbonate as an environmentally sustainable reagent to afford amino acid‐based aromatic poly(ester urea) homo‐ and copolymers with thermal properties that can be tuned by varying the chemical structure of the diamine monomer, or via copolymerization of two different monomers. [ABSTRACT FROM AUTHOR]

AbstractThis study presents a pore network (PN) model with transient heat transfer and quasi-steady transitional vapor transport that is for the first time applied to irregular porous structures that are obtained by reconstruction of X-ray tomography image data. In contrast to previous studies, the irregular pores are not approximated by spheres but implemented in their original shape. Secondly, instead of assuming cylindrical throats as pore connections, the actual distance between pore centers as well as the pore cross sections are used for the computation of the vapor transport coefficient. The control volume elements of the computational model are matched with the cells obtained by Voronoi tessellation. The improvements have clear advantages over former approaches where the reconstructed void space is usually strongly simplified by balls and sticks confined in a regular lattice structure. A freeze-dried sample of maltodextrin DE12 with 20% (w/w) solid content is used for benchmarking the new methodology. Its morphological and thermal properties are determined by the novel PN model. The simulation results of primary freeze-drying (FD) are compared to reference cases in two ways. First, the differences in heat and mass transfer kinetics as compared to regular PNs are emphasized. Secondly, the PN simulation results are confronted with a simple literature model that neglects pore size distribution (PSD) and transient heat transfer. It is shown that already in small domains with relatively narrow PSD, the variation of the mass transfer coefficient affects the computed sublimation fluxes and yields a significant deviation from the simpler literature model. Moreover, it is revealed in this study that the structure has a significant impact on the sublimation front temperature. This is demonstrated by the comparison of FD in the irregular PN to a regular PN with almost identical PSD but different porosity. The development, verification, and benchmarking of the new PN model can be seen as an important step for studies of the structure dependence of FD. [ABSTRACT FROM AUTHOR]

ABSTRACT Low‐temperature densification of alumina using calcium vanadate (CaV2O6, CV) having a similar dielectric constant as a liquid‐forming additive has been studied. The alumina‒CV composites containing 20‒40 vol.% CV achieve ∼94% of theoretical density at low temperatures of 1100°C‒900°C by liquid‐phase sintering. A reduction in the average size of grains from .87 to .42 µm with a surge in CV amount from 20 to 40 vol.% is observed. The permittivity decreases from 9.2 to 8.90, and the dielectric loss increases from 2.154 × 10‒3 to 4.761 × 10‒3 when the amount of CV in the alumina‒CV composite rises from 20 to 40 vol.%. The temperature coefficient of resonance frequency, thermal expansion coefficient, and thermal conductivity of the alumina‒CV composites are observed in the ranges of ‒54 to ‒72 ppm °C‒1, 6.94‒7.32 ppm °C‒1, and 13.78‒8.02 W m‒1 K‒1, respectively. The compatibility of the composites with Ag for low‐temperature co‐fired ceramics (LTCC) application is established through co‐sintering and energy‐Dispersive X‐ray spectroscopy line spectra analysis. The low‐temperature densification, acceptable range of dielectric and thermal properties, and silver compatibility make the alumina‒CV composite a candidate for LTCC application. [ABSTRACT FROM AUTHOR]

The high production cost and extremely weak mechanical properties of SiO 2 aerogels have been two major challenges hindering its widespread application. Atmospheric pressure drying (APD) has always been regarded as the optimal process to reduce costs. However, traditional APD is cumbersome, still uses a large amount of expensive raw materials, and is extremely immature. In this study, a novel APD was developed, inspired by the wing changes during adult damselfly process. Inorganic silica source/water was used as the raw material, and CO 2 was used instead of low surface tension solvent to stabilize the aerogel skeleton structure in situ, and ultimately aerogel material was obtained. The thermal conductivity of pure aerogels was as low as 0.0264 W/(m·K), the porosity reached 94.7 %, and the preparation cycle was only 28.5 h. The thermal stability of the skeleton structure and the chemical stability of surface were investigated and showed the hydrophobicity to withstand temperatures up to 400 °C. Aerogel composites feature low thermal conductivity of 0.0283 W/(m·K), and prominent thermal insulation properties over a wide temperature range of 50–300 °C. For traditional APD, this method shortens preparation cycle by 1–6 times. Compared with the commercial aerogel, the cost is reduced by 38.2 %, and the process is simple and environmentally friendly under the premise of ensuring excellent performance. [Display omitted] • A novel atmospheric pressure drying of aerogels preparation inspired by biology. • Stabilization of aerogel structures with CO 2 instead of low surface tension solvents. • The preparation cycle time is shortened by 1–6 times, the cost is reduced by 38.2 %. • Thermal conductivity of 0.0264 W/(m·K) and hydrophobic temperature resistance of 400 °C. • Aerogel composites have outstanding thermal insulation and moisture resistance. [ABSTRACT FROM AUTHOR]

Dy3+, Eu3+ co-doped glass ceramics (GCs) containing SrMoO 4 crystalline phase were prepared by melt-curing-crystallization method. The most favorable heat treatment conditions for the glass ceramics were found to be 610 °C/2 h by differential scanning calorimetry (DSC), ultraviolet spectrophotometer (UV–Vis), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The best doping concentrations of Dy3+ and Eu3+ in this glass ceramic were 0.8 % and 0.6 %, concentration quenching caused by dipole-dipole interactions occurs when the content of rare earth ions in GCs continues to increase. The chromaticity coordinates of the Dy3+- Eu3+ co-doped glass ceramics changed from cool white light to warm white light with the addition of Eu3+ concentration. At the optimal doping concentration (0.8 % Dy3+-0.6 % Eu3+), the chromaticity coordinate of glass ceramics is (0.3972, 0.3331), and the related color temperature is 3047 K. The luminescence intensity can still reach about 80 % of room temperature at 180 °C, and its thermal quenching activation energy is 0.233 eV. This suggests that glass ceramics have excellent thermal stability. After adding an appropriate amount of Li+, the crystalline phase of the glass ceramics remained unchanged and the luminous intensity of the glass ceramics increased by a factor of about 1.4 in the same environment. The thermal quenching activation energy of the glass ceramic doped with 0.2 % Li+-0.8 % Dy3+-0.6 % Eu3+ was 0.344 eV. The experimental results indicate that GCs has potential application prospects in the field of solid-state lighting. [ABSTRACT FROM AUTHOR]

This study describes the preparation of bimodal reinforced Cu/Ti 3 SiC 2 /C laminated-like composites using flake powder metallurgy and vacuum hot-press sintering process. The objective was to accurately modulate the formation of oriented reinforcement network in two-dimensional carbon materials. The powders used in the five designed composites were flake Cu powder (45–60 μm), Ti 3 SiC 2 (1–5 μm), graphite flakes (GFs, 120 μm) and graphene nanoplatelets (GNPs, 15 μm). Among them, the proportions of Ti 3 SiC 2 (10 wt %) and GFs (3 wt %) remained unchanged, GNPs accounted for 0 wt %, 0.5 wt %, 1.0 wt %, and 1.5 wt %, and Cu powder accounted for a decreasing proportion. Formation mechanisms of GFs and GNPs in oriented networks were quantitatively analyzed using the alignment model. Additionally, the related strengthening and failure mechanisms were investigated. According to the study, the bimodal laminated-like Cu/Ti 3 SiC 2 /C composites with 0.5 wt% GNPs added showed the best overall performance. Specifically, it exhibited a hardness of 125.7 HV, tensile strength of 276.3 MPa, thermal conductivity of 207.8 W m−1 K−1, and electrical conductivity of 23.6 MS/m. The network enhanced by the two-dimensional carbon material achieves efficient and orderly load transfer and dissipation mechanisms, optimizing stress distribution and enhancing fracture resistance, resulting in improved mechanical properties. In addition, the formation of the oriented reinforcement network optimizes the orientation arrangement of the reinforcing particles, which somewhat mitigates the scattering of thermoelectric carriers by structural defects in the composites, and the enlarged mean free-range improves the migration efficiency of electrons and phonons. Therefore, the erection of bimodal laminated-like structure achieves the goal of optimizing the properties of the composites. [ABSTRACT FROM AUTHOR]

Inspired by the significant catalytic charring effect of metal–organic frameworks (MOFs), Cu‐MOF decorated ammonium polyphosphate (APP@Cu‐MOF) was prepared by coupling agents to improve the fire safety of epoxy resin (EP). After adding 9 wt% APP@Cu‐MOF, the fire performance of EP is significantly improved with limiting oxide index (LOI) value of 29.4 and UL‐94 V‐0 rating. The peak heat release rate (PHRR), total smoke production (TSP), CO production, and CO2 production of EP composite samples decreased by 34.6%, 54.7%, 24.6% and 30.0%, respectively. It is proposed that the synergistic effect among Cu‐MOF and APP promoted the char formation of EP. The dense carbon layers formed a barrier that prevented the transfer of heat and inhibited the release of toxic gases, thus acting as a flame retardant. This work provides a new strategy to develop a high‐efficient MOF‐decorated flame retardant with smoke inhibition, toxicity reduction, and catalytic carbonization effect. [ABSTRACT FROM AUTHOR]

The escalating threat of bacterial infections to human health necessitates innovative antibacterial strategies and materials. Despite this need, there is still a significant demand for materials that combine high mechanical and thermal properties with biocompatibility. To address these urgent issues, our study investigates the development of poly(vinyl alcohol) (PVA) composite with graphene flakes (GF) as fillers. The aim is to strengthen the unique properties of graphene to enhance antibacterial activity. Graphene oxide (GO) was used as a surfactant to achieve stable graphene dispersion in water, preserving its inherent properties while avoiding the drawbacks associated with common surfactants, such as property reduction and complex removal processes. In this study, the mechanical and thermal properties of PVA composites containing GO and GF are superior to those of pristine PVA. Especially, the PVA‐2 composite exhibited a notable enhancement in both tensile strength and elongation at break compared with the PVA composite, with increases of 7.8% and 15% respectively. Moreover, PVA‐2, 4, and 6 composites exhibit significant antibacterial efficacy, achieving 4.8 and 4.9 log CFU/cm2 for Staphylococcus aureus and Escherichia coli, respectively. These results indicate that the enhanced oxidative stress induced by GO as a surfactant, combined with the physical damage caused by the increased GF nanostructures. This study highlights the potential of PVA/GF/GO composites in biomedical and tissue engineering applications, providing a promising pathway for the development of new antibacterial materials. [ABSTRACT FROM AUTHOR]

Currently, flexible thermal interface materials (TIMs) containing hexagonal boron nitride (h‐BN) as thermal conductive fillers become a research hot spot. In this study, PDMS@BN composite films were prepared using spin‐coating technology, providing a facile and efficient method for the preparation of TIMs. The effects of spin‐coating speed and time on the thermal conductivity and the orientation degree of BN within composite films were investigated. Additionally, a theoretical model was established to calculate the thickness and thermal conductivity of PDMS@BN composite films under various spin‐coating conditions. The findings indicate that with an increase of spin‐coating speed and extension of spin‐coating time, the thickness of the composite films gradually decreases, while the in‐plane and through‐plane thermal conductivity gradually increases. When compared to a low spin‐coating speed of 500 rpm, the thermal conductivity of the films produced by a higher speed of 2500 rpm, exhibited an increase of 274%. The film achieves outstanding thermal conductivity (5.79 W m−1 K−1), extremely thin thickness (60 μm), high volume resistivity (1.22 × 1013 Ω cm) and excellent flexibility by incorporating 60 wt % h‐BN flakes. Overall, this study presents an efficiently and eco‐friendly approach for high‐performance TIMs. [ABSTRACT FROM AUTHOR]