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Bi 4 Ti 3- x (Mg 1/2 W 1/2) x O 12 (BTMW100 x) ceramics were synthesized using a direct reaction method combined with a two-step sintering technique. The study systematically investigated the effects of B-site equivalent substitution of (Mg 1/2 W 1/2)4+ on BTMW100 x ceramics. The experimental results indicate that an appropriate amount of (Mg 1/2 W 1/2)4+ doping effectively reduces grain thickness, enhances grain distribution uniformity, and decreases the concentration of oxygen vacancies. Consequently, these modifications lead to improved piezoelectric performance while maintaining a high Curie temperature. Notably, Bi 4 Ti 2.95 (Mg 1/2 W 1/2) 0.05 O 12 (BTMW5) ceramics exhibit excellent piezoelectric properties and thermal stability, with a piezoelectric coefficient of 23 pC/N and a Curie temperature of 683 °C. These findings suggest that BTMW5 ceramics are promising candidates for high-temperature piezoelectric applications. [ABSTRACT FROM AUTHOR]

Six varieties of alkoxy polyhedral oligomeric silsesquioxanes (POSSs) featuring methoxy, ethoxy, n‐propoxy, isopropoxy, n‐butoxy, and n‐hexoxy as terminal groups were synthesized using the direct dehydrogenation condensation method. These POSSs were then incorporated as cross‐linking agents into hydroxy‐terminated polydimethylsiloxane (HPDMS) to create various formulations of room temperature vulcanized silicone rubbers (RTV SRs), denoted as SRM, SRE, SRP, SRI, SRB, and SRH. The morphology, thermal stability, and mechanical properties of the resulting SRs are analyzed using scanning electron microscopy (SEM), thermal gravimetric analysis (TGA) and universal tensile testing machine. The findings indicate that the incorporation of POSS into SRs results in significant enhancements in thermal stability and mechanical properties when compared to the control group (TEOS/SR). SRB and SRH exhibit the highest cross‐linking density and tensile strength. Specifically, SRB‐4 demonstrates the highest tensile strength at 2.66 MPa, representing an 8.6‐fold increase compared to TEOS/SR. The maximum decomposition rate temperature of SRP‐4 reaches 527°C and is 194°C higher than TEOS/SR. Because the alkoxy groups with different chain lengths on POSS have different chemical reactivity, they have a great effect on the dispersion of POSS in SRs, which affect the cross‐linking density, tensile strength, and thermal stability. [ABSTRACT FROM AUTHOR]

This study aimed to optimize the compatibility and performance of PLA/PC blends by investigating the effects of Cloisite 20A nanoclay (NC) and Joncryl chain extender (CE). PLA/PC blends with varying NC and CE loadings were prepared, and the optimal formulation was identified. The optimal NC and CE content were then used to produce PLA/PC blends with varying PC ratios. The test specimens were produced by mixing the mixture in a twin‐screw micro compounder and subsequent injection molding into dog bone specimens to investigate the thermal, mechanical, and morphological properties of the blends. Scanning electron microscopy and dynamic mechanical analysis confirmed the immiscibility of the unmodified blend, but significant improvements in blend morphology were observed with high NC/CE ratios. The presence of NC/CE resulted in reduced droplet size of dispersed PC phase and a new intermediate glass transition temperature (Tg) in DMA, suggesting partial miscibility. The highest thermal stability improvement was achieved with 5 wt% NC alone or a combination of 5 wt% NC and 1 wt% CE. Composites containing NC/CE showed the most significant improvements in composite properties, demonstrating their effectiveness as compatibilizers and improved compatibility in PLA/PC blends. These results indicate that the use of NC/CE is a promising method for expanding the applicability of PLA/PC blends. [ABSTRACT FROM AUTHOR]

Conductive polymer composites (CPC) are gaining increasing popularity due to their unique characteristics, which include light weight and the ability to conduct electricity. In this work, CPC were prepared by blending the polylactic acid (PLA) with a conductive filler, graphene nanoplatelets (GNP), at dosages ranging from 1 to 12 wt % using an internal mixer. The hot press machine was used to compress the CPC into thin sheet, and subsequently characterized for tensile, thermal, and electrical properties. The results showed that the addition of GNP at 7 wt % (percolation threshold) successfully transformed the PLA into an electrically conductive material. The tensile modulus increased with added GNP, but elongation at break and tensile strength exhibited an opposite trend. The incorporation of GNP also enhanced the composite's thermal stability. [ABSTRACT FROM AUTHOR]

In this study, ZnAlLa-maleate-LDHs was synthesized using the co-precipitation-hydrothermal method. The effects of aluminum-lanthanum ratio, co-precipitation time, hydrothermal time, and hydrothermal temperature on the crystal structure were investigated. As indicated by the result, the optimal condition was n (Al3+): n (La3+) = 10:1, the co-precipitation time reached 24 h, the hydrothermal time was 8 h, and the hydrothermal temperature reached 180°C. The effect of hydrotalcite on the thermal stability properties and plasticizing properties of PVC was analyzed. The result suggested that ZnAlLa-maleate-LDHs enhanced the thermal stability, plasticizing properties, and mechanical properties of PVC compared with ZnAlLa-CO3-LDHs. The layer spacing of hydrotalcite was increased with the introduction of maleic acid, such that the entry of Cl− into the interlayer guest was facilitated, and the decomposition of PVC was inhibited. Moreover, the long-term thermal stability mechanism was analyzed using FTIR before and after hydrochloric acid treatment. As revealed by the above result, the thermal stabilizer ZnAlLa-maleate-LDHs are capable of hindering the breakage of C-Cl bonds in PVC, inhibiting the formation of HCl, and playing a certain role in thermal stabilization. [ABSTRACT FROM AUTHOR]

Crude palm oil (CPO) is commonly used in the oil industry. This study presents a comparison of the structural, rheological, and thermal properties of clarified CPO (CCPO) sample obtained using the conventional method and ultrasound-assisted (UA)-treated samples. These samples were obtained in the pressed (press liquor, PL), sifted (sifted liquor, SL), and clarification (outlet sludge, OS) stages. The frequencies used for the UA-treated samples were 40 and 80 kHz for 30 min. The PL and SL samples exhibited higher resistance to oxidative deterioration and nutritional quality than the CCPO sample did. The maximum oil extractability percentage (OEP) of the UA-treated samples relative to that of CCPO was 7.4 %. The bleachability index (DOBI) values of the UA-treated samples were higher (between 2.06 and 2.58) than that of the CCPO sample (1.43). However, the viscosity (η) displayed opposite trend. The thermal stability did not exhibit consistent patterns with increasing frequency. [ABSTRACT FROM AUTHOR]

The crystallization thermal stability plays an essential role in affecting thermal stress of glass-ceramic sealant for long-term planar-type solid oxide fuel cells (SOFC) to prevent fuel leakage during operation. Due to the lack of systematic research on regulating the stable performance of glass-based sealant with the working time at operation temperature, herein, the effect of MgO on crystallization kinetics, phase stability, and thermal and mechanical properties of MgO–BaO–CaO–Al 2 O 3 –B 2 O 3 –SiO 2 (MBCABS) glass-ceramic has been firstly analyzed at heat-treatment of 750 °C with working time of 1∼1000h in this work. Subsequently, the relationship evolution of crystallization thermal stability-coefficient of thermal expansion (CTE) match-thermal stress was established by Finite Element Method (FEM). The main reasons for the decrease of CTE of MBCABS glass-ceramics with low-content MgO are the precipitation of hexagonal BaAl 2 Si 2 O 8 phase and the transformation of hexagonal BaAl 2 Si 2 O 8 to low-CTE monoclinic BaAl 2 Si 2 O 8 phase, bring about that the Von Mises thermal stress of sealant itself and interface having tripled at 1000h (more than 200 MPa) according to FEM simulation results. The thermal stable and high-CTE BaMgSiO 4 , Ba 8 Mg 16 Si 16 O 56 , and BaCa 2 Mg(SiO 4) 2 phases crystallized in MBCABS glass-ceramics with high-content MgO, therefore the maximum stress at all time parameters was below 100 MPa for 1∼1000h. This study was useful for identifying the optimal phase option and CTE matching of glass-based sealant for efficient and stable long-term operation of solid oxide fuel cells. [ABSTRACT FROM AUTHOR]

The over‐loading of heat‐resistant fillers in silicone rubber creates a contradiction between heat resistance and mechanical properties, thus greatly limiting the durability of silicone rubber products in cutting‐edge applications and complex scenarios. To address this issue, silicone rubber was filled with octavinyl polyhedral oligomeric silsesquioxane (POSS) and carbon nanotubes (CNT) and crosslinked with 2,5‐dimethyl‐2,5‐di(tert‐butylperoxy)hexane (DBPMH) in an attempt to obtain composites with excellent mechanical properties and great thermal stability. Optical microscopy and X‐ray diffraction analyses revealed the size of POSS crystals decreased and the characteristic peaks disappeared after the peroxide crosslinked the polymer at elevated temperature. Specifically, silicone rubber composite filled with 0.1 phr POSS and 1.0 phr CNT exhibited a tensile strength of 10.2 MPa and elongation at a break of 450%. Further, the strength and elongation could be kept after thermo‐oxidative aging at 250°C for 32 h. Thermogravimetric analysis results demonstrate that the addition of POSS and CNT into silicone rubber exhibits a synergistic effect, markedly improving the thermal stability of the material. This method provides a valuable reference for manufacturing silicone rubber products that possess both excellent mechanical properties and high thermal stability under extreme working conditions. Highlights: A novel silicone rubber composite with excellent mechanical properties and thermal stability was prepared.A small amount of octavinyl polyhedral oligomeric silsesquioxane (POSS) and carbon nanotubes exhibited a synergistic effect to improve thermal stability.The dependence of the morphological evolution of POSS crystals in SR on the 2,5‐dimethyl‐2,5‐di(tert‐butylperoxy)hexane and temperature was studied. [ABSTRACT FROM AUTHOR]

High‐density polyethylene (HDPE) nanocomposites containing different optimized fractions of carbon nanofiber (CNF) at 6 wt.%, polyethylene glycol (PEG) at 4 wt.%, and copper oxide (CuO) nanorods in concentration ranges of 0.15, 0.5, and 2 wt.% were successfully melt processed using corotating twin extrusion and compression molding technique. The effect of PEG and CuO nanofiller on the HDPE matrix were studied, particularly for the percolation threshold for electrical conductivity, structural morphology, and other properties including thermal stability, thermal conductivity (TC), dielectric, and UV protection properties. It is observed that PEG acts as a good compatibilizer, facilitating better interfacial connection between CNF and HDPE matrix. The optimized composite with 0.15 wt.% CuO nanorods (H/C6/P4/Cu0.15) shows a fine morphology and strong interfacial connections between fillers and the matrix, as observed in FE‐SEM micrographs. This optimized composite exhibits improved thermal stability, higher thermal conductivity (0.0404 W.K−1.m−1), increased dielectric constant, reduced electrical volume resistivity (from 2.1 × 1015 to 2.1 × 106 Ω.cm), and lower optical band gap value (2.74 eV). Additionally, all prepared nanocomposites offer approximately 100% Ultraviolet Protection Factor (UPF) rating for UV protection. Highlights: The transformation of insulating HDPE into conducting HDPE composites.The effect of CuO nanorods was investigated in compatibilized HDPE composites.A percolation is achieved in the HDPE composite at 0.15 wt.% of CuO nanorods.PEG and CuO nanorods improved the multifunctional properties of the composite. [ABSTRACT FROM AUTHOR]

A novel polycyclic naphthoxazine resin (NSA‐thiq) is synthesized via N, O‐acetal forming reaction between o‐hydroxyl naphthaldehyde and 1,2,3,4‐tetrahydroisoquinoline. The chemical structure of the monomer is investigated and confirmed by 1H and 13C NMR, Fourier‐transform infrared (FT‐IR) spectroscopy, and high‐resolution mass spectrometry. Besides, the ring‐opening polymerization behavior similar to ordinary benzoxazine resins is observed by differential scanning calorimetry (DSC) and in situ FT‐IR analyses, leading to the formation of the phenolic cross‐linked network. Notably, DSC thermograms indicate that the newly obtained polycyclic naphthoxazine resin exhibits much lower polymerization temperatures compared to many other reported benzoxazine or naphthoxazine resins. Moreover, the corresponding polybenzoxazine (poly(NSA‐thiq)) shows comparable thermal stability in comparison with thermosets derived from monobenzoxazine resins. As a consequence of these unique performances, NSA‐thiq is applied as a property modifier for a commercialized benzoxazine resin (BA‐a). The glass transition temperature of copolymeric thermosets is enhanced without sacrificing too much thermal stability and heat resistance. Here, another series of naphthoxazine thermosetting resin is explored, which can provide more examples for constructing composites based on thermoset polymers. [ABSTRACT FROM AUTHOR]

This work investigates the application of poly(3,4‐ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS) with polyethylene oxide (PEO) in lithium batteries (LIBs). This composite film comprising PEDOT:PSS and PEO was 3D printed onto a carbon nanofiber (CNF) substrate to serve as a layer between the polypropylene (PP) separator and the lithium anode in LIBs. The resulting CNF‐PEDOT:PSS‐PEO film exhibited superior mechanical and thermal properties compared to conventional PP separators. Mechanical tests revealed a high Young's modulus and puncture strength for the composite film. Thermal stability tests indicated that the CNF‐PEDOT:PSS‐PEO film remained stable at higher temperatures compared to the commercial PP separator, and combustion tests confirmed its superior fire‐resistance properties. In terms of conductivity, the composite film maintained comparable ionic conductivity to the commercial PP separator. Electrochemical tests demonstrated that LIBs incorporating the CNF‐PEDOT:PSS‐PEO film exhibited slight improvement in cycling performance, with a 7.9 % increase in long‐term cycling capacity compared to LIBs using only the commercial PP separator. These findings indicate that the developed CNF‐PEDOT:PSS‐PEO composite film holds promise to improve safety, while maintaining the electrochemical performance of LIBs by reducing dendrite formation and enhancing thermal stability. [ABSTRACT FROM AUTHOR]

The present study investigated the use of expanded perlite (e‐perlite) as a sustainable and cost‐effective filler for EPDM (ethylene propylene diene monomer) rubber composites. Various amounts of e‐perlite were incorporated into EPDM to assess its impact on the composite properties, such as curing characteristics, physical and mechanical properties, crosslink density, thermal conductivity, thermal stability, surface roughness, and contact angle. The composite with 15 phr of e‐perlite exhibited approximately 20% higher crosslink density and a 12% increase in hardness, while slight decreases were observed in elongation at break and tensile strength. The FE‐SEM (field emission‐scanning electron microscopy), atomic force microscopy, and contact angle analysis have been performed to investigate the surface morphology and the hydrophobicity. The thermal properties of the composites were assessed through thermogravimetric analysis, thermal aging tests, and thermal conductivity measurements. The results showed that e‐perlite significantly improved the aging resistance and the thermal stability. The composites with 15 phr e‐perlite exhibited a 21% reduction in thermal conductivity and enhanced thermal isolation properties compared to the EPDM composite without e‐perlite. This work demonstrated the potential utilization of e‐perlite in EPDM as a green sustainable filler to enhance the thermal insulation and the stability properties of the composites, which may have practical applications in automotive, aerospace, construction, and electronic industries. Highlights: E‐perlite enhances the thermal insulation property of EPDM rubber composites.Higher e‐perlite content increases composite hardness and crosslink density.The thermal conductivity of EPDM is reduced by increasing e‐perlite content.EPDM/e‐perlite exhibits improved thermal stability and aging resistance.Potential uses in automotive, aerospace, construction, and defense industries. [ABSTRACT FROM AUTHOR]

In this study, poly(butylene adipate‐co‐terephthalate) (PBAT) biocomposites were generated from spent coffee grounds (SCGs) or torrefied SCG (TSCGs) using a melt compounding process. TSCGs were obtained at torrefaction temperatures of 230, 245, 260, 275, or 290°C for a duration of 60 min. Torrefaction enhanced the hydrophobicity, grindability, and biomass stability of the resulting composites by eliminating hemicellulose. Various concentrations of SCGs (10 and 20 wt.%) and TSCGs (10, 20, and 30 wt.%) were compounded into PBAT. The thermal, mechanical, and degradation properties of PBAT biocomposites were investigated. As SCGs and TSCGs were introduced, the crystallization temperature drastically increased. Compared with PBAT biocomposites with SCGs, PBAT biocomposites with TSCGs exhibited higher thermal stability and hydrophobicity, and improved mechanical properties. Further, alkaline hydrolysis occurred at a faster rate for biocomposites with biofillers than for neat PBAT. Therefore, this study demonstrated the improved compatibility between SCGs and PBAT by torrefaction. [ABSTRACT FROM AUTHOR]

Levoglucosenone (LGO), a renewable compound obtained from cellulose biomass, has been utilized to prepare novel monomers bearing alkene functional groups. These monomer derivatives of LGO were subsequently cured via ultraviolet (UV)‐initiated radical thiol‐ene "click" chemistry with commercially available multifunctional thiols to obtain colourless, optically transparent cross‐linked thermosets. The monomers prepared in this work are unique due to utilising the internal double bond of the LGO ring during polymerization as part of the cross‐linked network. The thermal and mechanical properties along with the degradation of thermosets containing both ether and ester linkages within the LGO monomers were studied. These thermosets had tensile strengths of 1.3–3.3 MPa, glass transition temperatures between 23.2 and 27.2 °C, and good thermal stability of up to 300 °C. [ABSTRACT FROM AUTHOR]

Optically transparent polyimide (PI) films with good atomic oxygen (AO) resistance have been paid extensive attention as thermal controls, optical substrates for solar cells or other components for low Earth orbit (LEO) space applications. However, for common PI films, it is usually quite difficult to achieve both high optical transparency and AO resistance and maintain the intrinsic thermal stability of the PI films at the same time. In the current work, we aimed to achieve the target by using the copolymerization methodology using the fluorinated dianhydride 9,9-bis(trifluoromethyl)xanthene-2,3,6,7-tetracarboxylic dianhydride (6FCDA), the fluorinated diamine 2,2-bis [4-(4-aminophenoxy)phenyl]hexafluoropropane (BDAF) and the polyhedral oligomeric silsesquioxane (POSS)-containing diamine N-[(heptaisobutyl-POSS)propyl]-3,5-diaminobenzamide (DABA-POSS) as the starting materials. The fluoro-containing monomers were used to endow the PI films with good optical and thermal properties, while the silicon-containing monomer was used to improve the AO resistance of the afforded PI films. Thus, the 6FCDA-based PI copolymers, including 6FCPI-1, 6FCPI-2 and 6FCPI-3, were prepared using a two-step chemical imidization procedure, respectively. For comparison, the analogous PIs, including 6FPI-1, 6FPI-2 and 6FPI-3, were correspondingly developed according to the same procedure except that 6FCDA was replaced by 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA). Two referenced PI homopolymers were prepared from BDAF and 6FDA (PI-ref1) and 6FCDA (PI-ref2), respectively. The experimental results indicated that a good balance among thermal stability, optical transparency, and AO resistance was achieved by the 6FCDA-PI films. For example, the 6FCDA-PI films exhibited good thermal stability with glass transition temperatures (Tg) up to 297.3 °C, good optical transparency with an optical transmittance at a wavelength of 450 nm (T450) higher than 62% and good AO resistance with the erosion yield (Ey) as low as 1.7 × 10−25 cm3/atom at an AO irradiation fluence of 5.0 × 1020 atoms/cm2. The developed 6FCDA-PI films might find various applications in aerospace as solar sails, thermal control blankets, optical components and other functional materials. [ABSTRACT FROM AUTHOR]

Thermoplastic polyimides (TPIs) are promising lightweight materials for replacing metal components in aerospace, rocketry, and automotive industries. Key TPI attributes include low density, thermal stability, mechanical strength, inherent flame retardancy, and intrinsic fluorescence under UV light. The application of advanced manufacturing techniques, especially 3D printing, could significantly broaden the use of TPIs; however, challenges in melt-processing this class of polymer represent a barrier. This study explored the processability, 3D-printing and hence mechanical, and fluorescence properties of TPI coupons, demonstrating their suitability for advanced 3D-printing applications. Moreover, the study successfully 3D-printed a functional impeller for an overhead stirrer, effectively replacing its metallic counterpart. Defects were shown to be readily detectable under UV light. A thorough analysis of TPI processing examining its rheological, morphological, and thermal properties is presented. Extruded TPI filaments were 3D-printed into test coupons with different infill geometries to examine the effect of tool path on mechanical performance. The fluorescence properties of the 3D-printed TPI coupons were evaluated to highlight their potential to produce intricately shaped thermally stable, fluorescence-based sensors. [ABSTRACT FROM AUTHOR]

Polymerization of primary amine‐containing monomers is challenging because the amine inhibits polymerization catalyst activity. An alternative approach to access primary amine functionalized polymers is postpolymerization modification. To this end, the hydroaminoalkylation of vinyl‐terminated polyolefins with N‐(trimethylsilyl)benzylamine is used to prepare primary amine‐terminated polyolefins, with the free primary amine substituent being revealed upon hydrolytic work up. These materials are spectroscopically characterized, and an investigation of thermal properties by differential scanning calorimetry and thermogravimetric analysis is completed. These results show that the primary amine substituent increases the glass transition temperature and improves thermal stability. The reactive primary amine functionality is used in the photo‐oxidative dimerization of polyolefins to demonstrate how this elusive functionality can be applied in oligomer valorization. [ABSTRACT FROM AUTHOR]

AbstractFunctionally graded design transforms polymer composites without altering their properties. These composites change only the surface exposed to severe temperatures, leaving the rest unchanged. This study analyses ceramic additions’ effects on polymer thermal stability and crystallinity. Dynamic mechanical analysis (DMA) examined viscoelastic behaviour and thermogravimetric stability. Alumina, silicon carbide, and hafnium carbide ceramic powders increase thermal stability. DMA examined how ceramic additives affected composite viscoelasticity. The functionally graded design barely affects ceramic adhesive thermal properties. The ceramic adhesive remained stable at 800 °C with only 6% weight loss, while the other two disintegrated before 600 °C. [ABSTRACT FROM AUTHOR]

A novel phenylethynyl-terminated siloxane-containing ortho -hydroxy polyimide (O-SPI) was synthesized and physically blended with thermoplastic polyimide (PI) to enhance both the thermal and mechanical properties of polyimide, addressing the growing demand for high-performance materials in harsh environments. The blend underwent conversion to semi -Interpenetrating Polymer Networks (semi -IPNs) and benzoxazole structures through thermal curing of reactive phenylethynyl groups and thermal rearrangement of ortho-hydroxy imide units. The trends in thermal and mechanical properties were investigated in relation to the chemical structures and varying mass fraction of O-SPI. The covalent incorporation of semi -IPNs and rigid benzoxazole structures restrict segmental motion while the backbone linkage confers the toughness of the blends. These synergistic effects insure the cured blends with high glass transition temperatures (472.51°C) and tensile strength (117.81 MPa) simultaneously, demonstrating their potential for applications in challenging conditions. [ABSTRACT FROM AUTHOR]

Poly(butylene succinate) (PBS) exhibits many advantages, such as renewability, biodegradability, and impressive thermal and mechanical properties, but is limited by the low melt viscosity and strength resulted from the linear structure. To address this, vitrimeric network was introduced to synthesize PBS vitrimers (PBSVs) based on dynamic imine bonds through melt polymerization of hydroxyl-terminated PBS with vanillin derived imine containing compound and hexamethylene diisocyanate using trimethylolpropane as a crosslinking monomer. PBSVs with different crosslinking degrees were synthesized through changing the content of the crosslinking monomer. The effect of crosslinking degree on the thermal, theological, mechanical properties, and stress relaxation behavior of the PBSVs was studied in detail. The results demonstrated that the melt viscosity, melt strength, and heat resistance were enhanced substantially without obvious depression in crystallizability, thermal stability, and mechanical properties through increasing crosslinking degree. In addition, the PBSVs exhibit thermal reprocessability with mechanical properties recovered by more than 90% even after processing for three times. Furthermore, PBSV with improved melt properties shows significantly improved foamability compared to commercial PBS. This research contributes to the advancement of polymer technology by successfully developing PBS vitrimers with improved properties, showcasing their potential applications in sustainable and biodegradable materials. [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]

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]

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]

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]

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]

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]

In the present work, hybrid nanobiocomposites based on poly(3-hydroxybutyrate), P3HB, with the use of aromatic linear polyurethane as modifier and organic nanoclay, Cloisite 30B, as a nanofiller were produced. The aromatic linear polyurethane (PU) was synthesized in a reaction of diphenylmethane 4,4′-diisocyanate and polyethylene glycol with a molecular mass of 1000 g/mole. The obtained nanobiocomposites were characterized by the small-angle X-ray scattering technique, scanning electron microscopy, Fourier infrared spectroscopy, thermogravimetry, and differential scanning calorimetry, and moreover, their selected mechanical properties, biodegradability, and cytotoxicity were tested. The effect of the organomodified montmorillonite presence in the biocomposites on their properties was investigated and compared to those of the native P3HB and the P3HB-PU composition. The obtained hybrid nanobiocomposites have an exfoliated structure. The presence and content of Cloisite 30B influence the P3HB-PU composition's properties, and 2 wt.% Cloisite 30B leads to the best improvement in the aforementioned properties. The obtained results indicate that the thermal stability and mechanical properties of P3HB were improved, particularly in terms of increasing the degradation temperature, reducing hardness, and increasing impact strength, which were also confirmed by the morphological analysis of these bionanocomposites. However, the presence of organomodified montmorillonite in the obtained polymer biocomposites decreased their biodegradability slightly. The produced hybrid polymer nanobiocomposites have tailored mechanical and thermal properties and processing conditions for their expected application in the production of biodegradable, short-lived products for agriculture. Moreover, in vitro studies on human skin fibroblasts and keratinocytes showed their satisfactory biocompatibility and low cytotoxicity, which make them safe when in contact with the human body, for instance, in biomedical applications. [ABSTRACT FROM AUTHOR]

The development of high-power piezoelectric ceramics with superior piezoelectric properties and broad temperature usage ranges is vital for the thriving progress of electromechanical applications. However, achieving high piezoelectricity, high mechanical quality factor, and temperature stability often presents a trade-off. In this study, we present an advanced ceramic material with excellent high-power piezoelectric properties and superior temperature stability. The piezoelectric coefficient d 33 reaches 348 pC N−1, the electromechanical coupling factor k p is 54%, the mechanical quality factor Q m is 1501, the dielectric loss tanδ is 0.35%, and the d 33 variation is less than 10% within 25–210 °C in 0.05Pb(Mg1/3Nb2/3)O 3 -0.05Pb(Mn 1/3 Sb 2/3)O 3 -0.9Pb 0.95 Sr 0.05 (Zr 0.48 Ti 0.52)O 3 ceramic. The excellent piezoelectricity is attributed to the enhancement of intrinsic ionic displacement and reversible domains wall motion because of symmetry-conforming short-range distribution of oxygen vacancy, while the high Q m is a result of increased domain size and oxygen vacancy. The outstanding temperature stability is related to the stable non-180°domains structure due to the oxygen vacancy pinning effect. These properties hold great potential for advanced applications, particularly for piezoelectric high-power applications requiring constant d 33 over a broad temperature range. [ABSTRACT FROM AUTHOR]

One of the major challenges in expanding the uses of polymer materials is the development of thermally driven, multifunctional, self‐healing water polyurethanes with superior mechanical properties. By adding nano‐inorganic fillers and incorporating phenol‐carbamate bonds into the molecular chains, a self‐healing waterborne polyurethane with strong mechanical properties as well as antibacterial, and antiseptic properties was created. Given that tannic acid (TA) can create an isocyanate‐group‐containing phenol‐carbamate network, the resulting TA‐based water polyurethane (TWPU) had great mechanical properties and superior thermal stability with tensile strength of 31.9 MPa and elongation at break of 1406.4%. The amount of dynamic phenol‐urethane linkages in the polyurethane backbone can also be adjusted and controlled to achieve excellent self‐healing efficiency. The coating's anti‐corrosion properties were good when the waterborne polyurethane was added to ZnO modified GO. Furthermore, the coating exhibited strong antibacterial capabilities due to the incorporation of nano‐zinc oxide. In this study, we create an environmentally friendly waterborne polyurethane that is antibacterial, antiseptic, and self‐healing using a straightforward and efficient design approach. [ABSTRACT FROM AUTHOR]

There is an increasing demand for bio-based chitosan materials doped with synthetic polymers for sustainable production and economic development. Due to their helpful medical applications, chitosan-based nanocomposites containing ZnO nanoparticles (NPs) are very interesting. In the present study, new composite materials containing newly synthesized methacrylate-based polymer Poly(2-{[(2,4-chlorophenyl)methyl]amino}-2-oxoethyl-2-methylprop-2-enoate (PDCBMA), chitosan (CS) and biosynthesized ZnO NPs were produced by hydrothermal method. The composites were characterized by FTIR, XRD, SEM, EDX, and TEM. Synthetic PDCBMA blended with CS decreased the thermal stability of pure CS, but the addition of ZnO NPs slightly increased the thermal stability. Blending with PDCBMA and adding ZnO NPs increased the glass transition temperature (Tg) of pure CS. While the antibacterial activities of PDCBMA-CS/ZnO nanocomposites were significantly increased compared to CS, the antifungal effect was low. It was determined that ZnO NPs and PDCBMA included in the structure of CS were anticarcinogenic on A549 cells even at the lowest concentration (16 µg/mL). It was determined that the wound-healing effect of the PDCBMA-CS mixture was better than that of the control group, and the nanocomposite containing 3% ZnO NPs had a wound-healing activity close to the control group. The antimicrobial activity of the nanocomposite containing PDCBMA-CS blend and 3% ZnO NPs is higher than CS, so it is considered a good alternative as a substitute wound-healing material. [ABSTRACT FROM AUTHOR]

The red-emitting material SrBaMoO4:0.16Eu3+ was synthesized by using a high-temperature solid-state method. X-ray diffraction (XRD) and fluorescence spectroscopy were employed to analyze the crystal structure and luminescent properties. The results revealed that the sintering temperature had an influence on the crystal structure of the samples, with an optimal sintering temperature of 800℃. SrBaMoO4:0.16Eu3+ synthesized at 800℃ for 6.5 h exhibited a pure crystalline phase of SrBaMoO4. The luminescent intensity of the SrBaMoO4:0.16Eu3+ sample under excitation at 394 nm was tested at different temperatures. When the temperature reached 100℃, the luminescent intensity was 72.11% of the initial intensity, and the temperature reached 175℃, it dropped to 35.27% of the initial intensity. The sample demonstrated efficient excitation by blue light (464 nm), resulting the emission peak at 615 nm corresponding to the 5D0-7F2 transition of Eu3+. The luminescent intensity of the sample was found to increase with increasing Ba2+ concentration, reaching its maximum intensity when the Ba2+ doping concentration x was 0.27, followed by a gradual decreaseat excessive doping concentration, indicating concentration quenching. The CIE coordinates were calculated for the sample under excitation at 464 nm, revealing exhibited the best red emission at the Ba2+ doping concentration of x = 0.27. Additionally, first-principles calculations were used to determine the band structure and density of states of the sample. [ABSTRACT FROM AUTHOR]

Polymer coatings are widely used in industries for protection, decoration, and specific applications, typically including volatile organic compounds (VOCs) to achieve low viscosity. The growing environmental concerns and the anticipated limits on fossil feedstock have driven the coating industry towards eco-friendly alternatives, with UV-curing technology emerging as a promising solution due to its energy efficiency, low-temperature operation, reduced VOC emissions, and high curing speed. Polyurethane acrylates (PUAs) are critical in UV-curable formulations, offering excellent flexibility, impact strength, optical, and adhesion properties. However, UV-cured PUA coatings face limitations in thermal stability and tensile strength, which can be addressed by incorporating fillers. This study investigates the effects of multi-functionalized hexagonal boron nitride (hBN) nanoparticles on the mechanical, thermal, optical, and adhesion properties of UV-cured PUA films and coatings for pre-coated metals. The results demonstrated that incorporating hBN nanoparticles enhanced the mechanical and thermal properties of the nanocomposite films, with optimal performance observed at 0.5% hBN loading. Despite the improved properties, the FTIR spectra indicated that the low concentration of hBN did not produce significant changes, potentially due to the overshadowing signals from the difunctional polyurethane acrylate. [ABSTRACT FROM AUTHOR]

Characterization of isolated lignin and utilization of nanotechnology to produce nanolignin as a functional material are paramount. Lignin was extracted from acid-saccharification sugarcane trash (SCT-ASac) to produce acid-saccharification lignin (ASac-lignin). Then, lignin was further processed to nanolignin by a self-assembly dialysis process using THF:ethanol (1:1) as the solvent. The chemical, physical, and thermal properties of the lignin were evaluated, and the nanolignin size was confirmed via morphological analysis and PSA. SCT-ASac treatment prior to lignin isolation affects the structure of SCT and enhances the accessibility of lignin. Furthermore, this pretreatment can reduce residual carbohydrates, increasing the purity value. ASac-lignin has a nonconjugated phenolic group structure with a high number of β-O-4 bonds, a syringyl content, aromatic groups with low thermal stability, and a molecular weight with good phenolic hydroxyl content and total phenolic compounds. The obtained nanolignin is a spherical and more uniform particle with sizes less than 100 nm. ASac-nanolignin has the potential to be an environmentally friendly material in derivative lignin synthesis. [Display omitted] • acid-saccharification treatment of sugarcane trash to improve lignin accessibility. • the higher purity (94.23 %) was ASac-lignin. • ASac-lignin has good chemical traits, low thermal stability, and molecular weight. • nanolignin preparation using THF: Ethanol (1:1) and dialysis process. • ASac-nanolignin has a spherical shape with a particle size below 100 nm. [ABSTRACT FROM AUTHOR]

The segment character of polyurethanes (PUs) determines the micromorphology and properties. The effective segment regulation can customize the favorable performance of PUs. Herein, silicon covalent‐modified polyurethanes (MPUs) were prepared by incorporating diphenylmethane diisocyanate (MDI) and diphenyl silanediol (DPSD) into PU molecules as hard segments via a two‐step method. Distinctive microphase separation structures from sheet morphology to radial sheet or withered flower‐like microdomain were formed by adjusting hydrogen bonding of hard segments and post‐treatment techniques. Thus, with the addition of DPSD in hard segments, the thermo‐optic responses for MPUs occurred due to the different microphase evolution under thermal effect. And with the further addition of DPSD, the effect of thermal stimuli on the transmittance gradually weakened. It was very clear that with increasing the temperature, the transmittance of MPUs showed a gradual increase owing to melting the microcrystals or destroying the ordered accumulation of hard segments. Meanwhile, the high mechanical properties were obtained, higher 15 times tensile strength and more than 100 times elastic modulus than those of pure PU as well as the excellent thermal stability. In sum, this study was of great significance for developing new functionalized PU materials. Highlights: Polyurethanes were prepared by inducing modified silicon functionality.The distinctive microphase separation evolution of MPUs was found.Thermal stimuli responses showed a gradual decrease due to different structure.High mechanical properties and thermal stability were also obtained. [ABSTRACT FROM AUTHOR]

Bismaleimide (BMI) resins is widely used in the aerospace field because of its excellent properties, but its poor toughness limits the possibility of its application in a wider range of fields. Therefore, a novel bio‐compound, 4‐(allyloxy)‐3‐methoxy‐N‐(3‐(triethoxysilyl)propyl)benzamide (AMTPM), was designed and synthesized from renewable vanillin, which has Schiff‐base structure, silico‐oxygen bond structure, and allyl structure. The chemical structure of AMTPM has been characterized and validated by Fourier transform infrared (FTIR) and hydrogen nuclear magnetic resonance (1H NMR). It was found that the addition of AMTPM can effectively promote the curing behavior of BD resins (BMI and diallyl bisphenol A (DBA) was mixed and cured at the ratio of 1:0.87, named BD resins). AMTPM can affect the thermal stability and improve the mechanical properties of BD‐AMTPM resins (BD resins modified by AMTPM in different addition), and the detailed discussion was conducted. With the increase of AMTPM content, the thermal stability of BD‐AMTPM resins was deteriorated while the residual weight percentage at 800°C (Yc) was increased. When the content of AMTPM reached 12 wt%, the results showed that Yc achieved the values at a magnitude of 37.57%. Meanwhile, the glass transition temperature (Tg) achieved 320°C. Among the BD‐AMTPM resins system, the BD‐6 wt% AMTPM has the best toughness and mechanical properties. The impact strength was increased by 29.2%, the tensile strength was increased by 22.1% and the elongation at break was increased by 44%. The fracture morphology of BD‐AMTPM resins was also studied by scanning electron microscopy (SEM) to support the mechanical experimental conclusions. This study provides a more environmentally friendly and convenient modifier, which is of great significance for expanding the application of bismaleimide resin. Highlights: A bio‐based modifying agent (AMTPM) was designed and successfully synthesized.AMTPM has both Si‐O and Schiff‐base structures.AMTPM can effectively improve the toughness of BD‐AMTPM resins through impact and tensile tests. [ABSTRACT FROM AUTHOR]

Highlights To improve the subpar lubricating performance of epoxy resin, this paper presents the preparation of a novel bimetallic phyllosilicate featuring a distinctive rice‐granular morphology, which incorporates nickel and iron metal cations through a facile hydrothermal process. These phyllosilicates were then integrated into the epoxy matrix to form composites. A comprehensive analysis of the target product validates the rationality of the synthesis strategy for the as‐prepared rice‐granular bimetallic nickel/iron phyllosilicate, demonstrating a homogeneous hierarchical structure with numerous tiny nanosheets of nickel/iron phyllosilicate grown in situ on the flat surfaces of the rice‐granular metal–organic frameworks. An adequate addition of nickel/iron phyllosilicates allows for excellent dispersion within the matrix and establishes strongly bonded interfaces, steadily increasing the elastic modulus and hardness. Notably, the average friction coefficients decrease from 0.515 for the pure resin to 0.450 for the composites when the filler content reaches 7%, indicating a significant solid lubrication effect. In contrast, adding just 1% nickel/iron phyllosilicate moderately improves wear resistance, elongation at break, and tensile strength. Furthermore, it was found that as the filler content increased, the weight loss rate was reduced by approximately 43.8%, while the residual char increased by 74.2%, significantly enhancing the thermal stability of epoxy composites at high temperatures. This study offers a promising approach to preparing self‐lubricated epoxy composites with favorable mechanical and thermal properties. NiFePS was successfully synthesized via a facile two‐step self‐polymerization. Excellent mechanical properties of composites could be achieved with low content of NiFePS. The friction coefficient and wear rate were lowered remarkably. The friction mechanism was solid lubrication. [ABSTRACT FROM AUTHOR]

Highlights This study investigated the effect of multi‐walled carbon nanotubes (MWCNTs) and reclaimed gypsum of varying contents on the mechanical properties and thermal stability of polypropylene (PP) composite materials. The results indicated that the incorporation of reclaimed gypsum and MWCNTs powder into PP composites could enhance the tensile strength, impact strength, and bending modulus of PP to a certain extent. The above properties of AGY/MWCNTs/PP composites were increased by 14.6%, 131.8%, and 36.2%, respectively, with the impact properties being significantly affected. Univariate analysis of variance revealed that MWCNTs powder and recycled gypsum exerted a significant impact on the mechanical properties of polypropylene composites. Moreover, the initial weight loss temperature of AGY/MWCNTs/PP demonstrated a notable increase, from 318.71 to 398.48°C, while the maximum weight loss temperature exhibited a comparable rise, from 406.85 to 461.54°C. The impact performance and thermal stability of polypropylene composite materials have been demonstrably augmented. A synergistic effect between reclaimed gypsum and multi‐walled carbon nanotubes in the reinforcement of polypropylene composites was demonstrated. This provides a theoretical framework and practical guidance for the design and preparation of high‐performance and recyclable polymer composites. [ABSTRACT FROM AUTHOR]

Background Results Conclusion Fried dough sticks, widely enjoyed in southeast Asia, are made by frying a mixture of wheat flour and water at high‐temperature. With the move towards industrial production, there is an increasing demand for healthier versions. Understanding the key properties of fried dough sticks and how the ingredients interact is crucial for meeting these health‐focused consumer preferences.In this study, the connections between the dough's rheological and thermal properties, alongside the interactions between gluten proteins and the oil content in fried dough sticks, were examined and analyzed at varying gliadin to glutenin mass ratios (Gli/Glu). The results indicated that a general decrease in the viscoelastic properties of the dough was associated with an increase in the Gli/Glu ratio. Furthermore, a heightened concentration of gliadin was observed to augment the mass loss of gluten proteins, thereby engendering a spatially sparse network structure. Additionally, this excessive presence of gliadin precipitated the thermal instability within the dough, necessitating an augmented chemical force to preserve the stability of the gluten network structure.At the Gli/Glu ratio of 5:5, the gluten protein exhibited enhanced thermal stability and minimal mass loss. At this specific ratio, the gluten network was characterized by a comparatively high prevalence of extended gluten films and short‐chain structures, which resulted in the production of fried dough sticks possessing minimal structural oil content. The study provided a theoretical basis for identifying the Gli/Glu ratio as an effective approach to modulate the oil content in fried dough sticks. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

In this study, graphene nanoplatelets were applied to polyester fabrics using the knife‐coating method at different concentrations (50, 100, and 150 g/kg). SEM, DSC, and TGA/DTG analyses were performed. The influence of graphene coating on hydrophobicity and surface roughness was examined by water contact angle (WCA) measurement and root mean square roughness, respectively. Abrasion resistance and tear strength tests were also performed. The effect of graphene used as a filler on the flammability of polyester fabric was evaluated for the first time according to the BS 5852 standard. No significant weight loss (only in the range of 0.4%–1.5%) was observed in the graphene‐coated samples even after 100,000 cycles. While the WCA value was 0 for the uncoated fabric, the blind coating and maximum graphene‐coated sample measured 86° and 95°, respectively. The coating process reduced the roughness of the base fabric, and the decrease continued with the increasing graphene ratio. The tear strength values that were 45.5 N in the warp and 53.6 N in the weft direction in the blind coating, increased to 52.2 and 59.1 N, respectively, at the maximum graphene concentration. Graphene coating enhanced thermal stability, increased hydrophobicity, and improved flame retardancy in the test using a smoldering cigarette. [ABSTRACT FROM AUTHOR]

In this paper, a novel composite phase change material (CPCM) is prepared with inorganic PCM through impregnation and dispersion method which can be used for thermal management applications. Inorganic PCMs have high latent heat and good thermal conductivity and are non-flammable, but there exist leakage (shape stability) and corrosion problems. To overcome these issues, a porous structured material is impregnated with the inorganic PCM (disodium hydrogen orthophosphate dodecahydrate). The CPCM is prepared by loading various wt% of expanded graphite and boron nitride nanoparticles with the PCM, and characterization is performed to find the thermal properties and stability. The findings from FTIR and XRD analyses validate both the chemical compatibility and crystalline nature of the samples. DSC thermographs reveal the CPCM5 sample has a latent heat value of 168.05 J/g during the heating process, an encapsulation efficiency of 78.8% and a thermal conductivity of 4.69 W/mK. The thermal stability and resistance to corrosion of the composite samples are also enhanced. The best composite PCM sample is then selected, and subsequently, the thermal performance of the heat sink is experimentally investigated. The thermal performance of rectangular cavity heat sink filled with CPCM5 is the highest for various power sources and temperatures with a maximum enhancement ratio of 6.57. [ABSTRACT FROM AUTHOR]

Epoxy resins, known for their excellent properties, are widely used thermosetting resins, but their tendency towards brittle fracture limits their applications. This study addresses this issue by preparing graphene oxide via the Hummer method, modifying it with hyperbranched polyamide ester, and reducing it with hydrazine hydrate to obtain functionalized graphene. This functionalized graphene improves compatibility with epoxy resin. Using a novel two-phase extraction method, different ratios of functionalized graphene/epoxy composites were prepared and tested for mechanical properties and thermal stability. The results showed significant improvements: the tensile strength of composites with 0.1 wt% functionalized graphene increased by 77% over pure epoxy resin, flexural strength by 56%, and glass transition temperature by 50°C. These enhancements, attributed to the improved compatibility between graphene and epoxy resin, demonstrate the potential of functionalized graphene to mitigate the brittleness of epoxy resins, expanding their application potential. [ABSTRACT FROM AUTHOR]

Although significant efforts have been undertaken to explore the toughening of epoxy resins, it remains challenges to establish a simple and effective toughening technique which does not compromise its strength, thermal stability and processing performance. In this paper, toluene‐diisocyanate‐trimer (TDI‐T) was utilized to manufacture a novel epoxy‐terminated dendritic modifier TDI‐T glycol diglycidyl ether (TDI‐T GLDE). When the addition of TDI‐T GLDE reaches 20% of the resin mass, the tensile strength, tensile elongation, compressive strength and impact strength were increased by 28.1%, 75%, 24.8%, and 138.0% respectively, compared to E‐51. The thermal properties of the samples have been improved, including an increased glass transition temperature (Tg) from 68.2 to 73.2°C, as well as an increase in the initial decomposition temperature from 240.6 to 257.7°C. The toughening mechanism of TDI‐T GLDE was studied through a combination of mechanical performance tests, thermal performance tests, and resin fracture surface morphology analysis. [ABSTRACT FROM AUTHOR]

A lithium‐ion battery separator facilitates lithium‐ion transportation and prevents direct contact between the cathode and anode. Polyimide separators exhibited superior thermal stability and electrolyte wettability. In this study, carboxylated polyimide separators were prepared by electrospinning carboxyl group‐containing monomers. Polyimide separators were prepared with different content of carboxyl group‐containing monomer. Moreover, the thermal property, mechanical property, and electrochemical performance of separators were studied. The carboxylated polyimide separators exhibited lower interfacial resistance and higher ionic conductivity compared with polyimide separators. Moreover, the LiFePO4/Li half‐cell assembled using the carboxylated polyimide exhibited enhanced cycling stability and rate capability. Therefore, carboxylated polyimide separators with superior electrochemical performances are promising candidates for lithium‐ion batteries. [ABSTRACT FROM AUTHOR]

Phosphors with multifunctional applications have attracted extensive research, especially in thermometer and anti‐counterfeiting fields. Herein, a series of Pr3+‐doped YNbO4 (YNO) phosphors with adjustable photoluminescence and red persistent luminescence (PersL) performances are developed. YNO host exhibits the blue self‐activated luminescence, and the different Pr3+ emission peaks possess various thermal stability properties due to the thermal quenching channel generated by the intervalence charge transfer state between Pr3+ and Nb5+ ions. Two kinds of fluorescence intensity ratio models with high absolute and relative sensitivities are realized to measure the temperature under dual‐wavelength excitation. Moreover, YNO:Pr3+ exhibits the red PersL with a duration of about 120 s upon ceasing the UV excitation light source. The fabricated YNO:Pr3+‐polydimethylsiloxane films display different luminescence patterns with the passage of time after turning off UV light, which can cleverly achieve dynamic conversion. These results demonstrate that YNO:Pr3+ phosphor has potential applications in dual‐wavelength excited thermometry and dynamic anti‐counterfeiting fields. [ABSTRACT FROM AUTHOR]

Highlights A fluorinated polyimide (PI‐FTD) was synthesized for preparing a thermally conductive PI matrix and composites. Additionally, surface‐treated boron nitride (BN) was incorporated into the PI‐FTD via the solution casting method to form efficient heat paths along the through‐plane direction. The resultant composite demonstrated remarkable characteristics, including an impressive through‐plane thermal conductivity of 3.6 W mK−1, a substantial tensile strength of 69.4 MPa, and excellent thermal stability. When this composite was applied to light‐emitting diodes, it effectively managed heat, reducing the operating temperature by 29°C. The PI‐FTD/BN‐OH composites can potentially improve thermal management in electronic devices. A novel fluorinated polyimide (PI‐FTD) was fabricated. Introducing CF3 functionalities in the PI‐FTD provides high thermal stability. BN‐OH reinforced the thermal and mechanical properties of the composites. The PI‐FTD/BN‐OH composites achieved excellent thermal management. [ABSTRACT FROM AUTHOR]

The annual changes of the scallop’s adductor muscle in Ca2+-ATPase activity, chymotryptic digestion, endogenous fluorescence spectra, sulfhydryl content, and surface hydrophobicity were studied. Ca2+-ATPase activity peaked in February and reached its minimum in August for males and in July for females. However, no significant differences were observed between males and females throughout the year. The inactivation rate of Ca2+-ATPase activity increased by 17- to 36-fold when the temperature rose from 38°C to 45°C. The ratio of free myosin to bound myosin was approximately 5:4 at 0.5  M KCl and changed to 5:1 at 1.0  M, as determined by modeling. Chymotryptic digestion demonstrated that scallop myosin could be cleaved into S-1/rod portions at 0.1  M and HMM/LMM at 0.5  M KCl. Furthermore, no significant seasonal variations were observed in chymotryptic digestion patterns, endogenous fluorescence, surface hydrophobicity, or sulfhydryl content. In conclusion, the structure and thermal stability of both male and female scallops remained stable throughout the year, making them suitable for processing and preservation. [ABSTRACT FROM AUTHOR]

Bast fiber-reinforced polymer composites (BFRPs) are grabbing considerable research attention due to their assertive impact on the environment and excellence in biodegradability. Though BFRPs have excellent ecological performance factors, they also lack in some cases, such as lower mechanical, electrical, and thermal properties, due to the significant moisture absorption, minimal thermal stability, and inherent nature of bast fibers. BFRPs exhibit weaker fiber/matrix interfacial adhesion as compared to synthetic fiber-reinforced polymer composites, resulting in lower mechanical properties. Nowadays, a wide variety of fiber and matrix modification techniques are practiced improving the fiber-matrix interaction, which ultimately improves the mechanical properties. Among the fiber and matrix modification techniques, nanofiller integration is the most promising one. This study reviews the impacts of introducing carbon-based nanofillers, particularly graphene and carbon nanotubes (CNT), in diversified BFRPs. The influence of carbon-based nanofillers on the mechanical, electrical, and thermal behavior of BFRPs and their potential prospects are comprehensively reviewed. The paper concludes with the challenges and difficulties in composite processing, along with the techniques for overcoming them. [ABSTRACT FROM AUTHOR]

The traditional high-temperature preparation process of polyimide can cause many problems and limits the wider application in extreme conditions. An important challenge to be solved urgently is the reduction of imidization temperature. In this work, twelve kinds of polyimide films with different chain rigidity were prepared at low temperature of 200 °C, in the absence or presence of imidazole used as the catalyst. The molecular rigidity and free volume were theoretically calculated, and relationship between structure and properties were systematically studied. The results show that imidization reaction under low temperatures is significantly affected by the rigidity of molecular chains. The rigid structure of polyimide is not conducive to the low-temperature imidization, but this adverse effect can be eliminated by adding catalyst, resulting the notably increased imidization degree. The optical and thermal properties can be improved to a certain extent for the chemically catalyzed system, resulting in relatively higher heat resistance and thermal stability. While the mechanical performance could be determined by complicating factors, greatly different from polyimide films prepared by high temperature method. To investigate aggregation structures of films, the effect of chain rigidity and catalyst on the stacking or orientation of molecular chains was further elaborated. This work can contribute to the understanding of chemically catalyzed imidization that is rarely reported in the existing research, and will provide guidance for the low-temperature preparation of high-performance polyimides. [ABSTRACT FROM AUTHOR]

We report a transformative epoxy system with a microalgae-derived bio-binder from hydrothermal liquefaction processing (HTL). The obtained bio-binder not only served as a curing agent for conventional epoxy resin (e.g., EPON 862), but also acted as a modifying agent to enhance the thermal and mechanical properties of the conventional epoxy resin. This game-changing epoxy/bio-binder system outperformed the conventional epoxy/hardener system in thermal stability and mechanical properties. Compared to the commercial EPON 862/EPIKURE W epoxy product, our epoxy/bio-binder system (35 wt.% bio-binder addition with respect to the epoxy) increased the temperature of 60% weight loss from 394 °C to 428 °C and the temperature of maximum decomposition rate from 382 °C to 413 °C, while the tensile, flexural, and impact performance of the cured epoxy improved in all cases by up to 64%. Our research could significantly impact the USD 38.2 billion global market of the epoxy-related industry by not only providing better thermal and mechanical performance of epoxy-based composite materials, but also simultaneously reducing the carbon footprint from the epoxy industry and relieving waste epoxy pollution. [ABSTRACT FROM AUTHOR]