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Bisphenol A epoxy resin cured with a mixture of dimerized and trimerized fatty acids is the first epoxy vitrimer and has been extensively studied. However, the cure behavior and thermal and mechanical properties of this epoxy vitrimer depend on the epoxy/acid stoichiometry. To address these issues, epoxy vitrimers with three epoxy/acid stoichiometries (9:11, 1:1 and 11:9) were prepared and recycled four times. Differential scanning calorimetry (DSC) was used to study the cure behavior of the original epoxy vitrimers. The dynamic mechanical properties and mechanical performance of the original and recycled epoxy vitrimers were investigated by using dynamic mechanical analysis (DMA) and a universal testing machine. Furthermore, the reaction mechanism of epoxy vitrimer with different epoxy/acid stoichiometry was interpreted. With an increase in the epoxy/acid ratio, the reaction rate, swelling ratio, glass transition temperature and mechanical properties of the original epoxy vitrimers decreased, whereas the gel content increased. The recycling decreased the swelling ratio and elongation at break of the original epoxy vitrimers. Moreover, the elongation at break of the recycled epoxy vitrimers decreased with the epoxy/acid ratio at the same recycling time. However, the gel content, tensile strength and toughness of the original epoxy vitrimers increased after the recycling. The mechanical properties of epoxy vitrimers can be tuned with the variation in the epoxy/acid stoichiometry.

Molecular dynamics (MD) simulations were carried out to predict the thermal and mechanical properties of the cross-linked epoxy system composed of DGEBA resin and the curing agent TETA. To investigate the effects of curing agents, a comprehensive and comparative study was also performed on the thermal and mechanical properties of DGEBA/TETA and DGEBA/DETDA epoxy systems such as density, glass transition temperature (Tg), coefficient of thermal expansion (CTE) and elastic properties of different cross-linking densities and different temperatures. The results indicated that the glass transition temperature of DGEBA/TETA system calculated through density-temperature data, ∼ 385-395 °K, for the epoxy system with the cross-linking density of 62.5% has a better agreement with the experimental value (Tg, ∼ 400 °K) in comparison to the value calculated through the variation of cell volume in terms of temperature, 430-440 °K. They also indicated that CTE related parameters and elastic properties including Young, Bulk, and shear's moduli, and Poisson's ratio have a relative agreement with the experimental results. Comparison between the thermal and mechanical properties of epoxy systems of DGEBA/TETA and DGEBA/DETDA showed that the DGEBA/DETDA has a higher Tg in all cross linking densities than that of DGEBA/TETA, while higher mechanical properties was observed in the case of DGEBA/TETA in almost all cross linking densities., (Copyright © 2015 Elsevier Inc. All rights reserved.)

In order to prepare highly heat-resistant packaging insulation materials, in this paper, bismaleimide/epoxy resin (BMI/EP55) composites with different contents of BMI were prepared by melt blending BMI into amino tetrafunctional and phenolic epoxy resin (at a ratio of 5:5). The microstructures and thermal and electrical properties of the composites were tested. The electrostatic potential distribution, energy level distribution, and molecular orbitals of BMI were calculated using Gaussian. The results showed that the carbonyl group in BMI is highly electronegative, implying that the carbonyl group has a strong electron trapping ability. The thermal decomposition temperature of the composites gradually increased with the increase of BMI content, and the 20% BMI/EP55 composites had the highest heat-resistance index, along with a glass transition temperature (Tg) of >250 °C. At different test temperatures, with increase in the BMI content, the conductivity of epoxy resin composites showed a tendency to first decrease and then increase, the breakdown field strength showed a tendency to first increase and then decrease, and the dielectric constant was gradually decreased. Two trap centers were present simultaneously in the composites, where the shallow trap energy level is the deepest in 20% BMI/EP composites and the deep trap energy level is the deepest in 10% BMI/EP55 composites. Correspondingly, the 10% BMI/EP55 composite had a slower charge decay rate, while the 20% BMI/EP55 had a faster charge decay rate. In summary, the BMI/EP55 composites with high heat resistance and insulating properties were prepared in this study, which provided ideas for preparing high-temperature packaging insulating materials. [ABSTRACT FROM AUTHOR]

The aim of this research was to investigate asphalt effects on the storage stability, mechanical properties and micro‐properties of cold‐mixed epoxy asphalt binder (CEAB). Firstly, four CEAB were prepared with four base asphalt types and storage stability, miscibility analyses were performed by fluorescence microscopy (FM). Then, cured CEAB and epoxy resin (ER) were treated by ultraviolet aging. Tensile test, dynamic mechanical analysis (DMA), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy were applied to clarify the mechanical properties and micro‐properties of aged and unaged CEAB. Also, bending beam rheometer (BBR) tests were conducted to study low‐temperature performance of CEAB. The results revealed that the CEAB prepared with asphalt with penetration grade 60 ~ 80 presented superior storage stability, miscibility, mechanical properties and that prepared with penetration graded 80 ~ 100 showed slightly better low‐temperature performance. Moreover, asphalt properties were found to have little impacts while epoxy resin played a key role in the mechanical properties of CEAB. Glass transition temperature (Tg) of the CEAB containing penetration‐graded asphalt 80 ~ 100 decreased more significantly than that with penetration‐graded asphalt 60 ~ 80, and it was also found that the CEAB prepared with base asphalt with higher molecular weight polydispersity index had better ductility performance. [ABSTRACT FROM AUTHOR]

Highlights To predict the coefficient of thermal expansion (CTE) of carbon fiber/epoxy resin composites with void defects comprehensively and accurately, a comprehensive study is carried out by integrating experiment, analytical model (ANM), and finite element model (FEM). The experiments on composites are conducted combining with Micro‐CT to provide geometric parameters and verification for ANM and FEM. An ANM considering void defects is established based on the Chamis model to investigate the influence of porosity, temperature and the ratio of modulus of the constituents of composites. A FEM is established to verify the ANM and reveal the mechanisms of the influence of void defects. The results show that the proposed ANM has high agreement with FEM and experiment. The longitudinal CTE decreases by 61.94% as the porosity increases from 0% to 20% at 60°C, and the same change of porosity results in a 15.62% decrease at 180°C. The transverse CTE is less susceptible to changes in porosity, showing reductions of 2.32% at 60°C and 3.33% at 180°C. An innovative model is proposed to predict CTE considering void defects. The glass transition temperature Tg of the resin has a significant effect on CTE. Void defects change the homogeneity of the original stress field of the matrix. The reduction of the longitudinal CTE caused by void defects is more significant. [ABSTRACT FROM AUTHOR]

Water-based coating has gained much attention globally due to environmental issues. This work aims to develop a waterborne epoxy coating incorporated with modified natural rubber (NR) latex for improved performance. For this purpose, the NR latex was modified into three types of low molecular weight epoxidized natural rubber (LENR) latex. The waterborne epoxy resin was prepared by simply mixing the epoxy resin with an amine curing agent in water and various LENR latex contents (10 to 50 wt%). The waterborne epoxy/LENR blend was coated on a tin substrate and the cured coating demonstrated better adhesion and bending properties than the neat epoxy. Phase morphological properties displayed a rough surface with a heterogeneous surface structure of the dispersed rubber and epoxy matrix. Two glass transition temperatures were observed, corresponding to the rubber modifier and the epoxy matrix. The mechanical properties of the thermosetting epoxy/LENR blends were assessed, revealing a maximum increment in elongation ability by approximately 370% for adding 50 wt% LENR, compared to the neat epoxy. These results hold the potential avenue for utilizing NR-based material in the waterborne epoxy-based resin for coating applications. Furthermore, it contributes to the NR, a renewable and eco-friendly material, in the coating technology, embracing a sustainable future. [ABSTRACT FROM AUTHOR]

Type V linerless hydrogen storage vessels made of all-composite face the challenges of cryogenic mechanical failure and hydrogen leakage of composites. The cryogenic mechanical performance and gas-barrier property of the carbon fiber reinforced polymer for Type V vessels are largely determined by the epoxy matrix. Carbon nanotubes are widely used as polymer reinforcement material to enhance the cryogenic mechanical performance and gas-barrier property of epoxy resins. In this work, multi-walled carbon nanotubes (MWCNTs) were dispersed into epoxy resins to prepare MWCNTs-modified epoxy resins. The cryogenic mechanical performance, gas-barrier and thermal properties of the modified resin were then investigated. The experimental findings revealed a 34.34% reduction in the gas permeability coefficient for the nanocomposites containing 0.9 wt% MWCNTs compared with the epoxy matrix. The tensile strength and failure strain at cryogenic temperature (77 K) experienced enhancements of 26.99% and 41.53%, respectively. In addition, the thermal stability and glass transition temperature of the modified resin were improved. As a result, the MWCNTs-modified epoxy resin exhibits improved gas-barrier property in addition to excellent cryogenic mechanical performance, making it ideal for manufacturing Type V linerless hydrogen storage vessels. • The thermal stability and glass transition temperature of the modified resin are improved. • The tensile strength and failure strain at 77 K improved by 26.99% and 41.53%, respectively. • The gas permeability coefficient of MWCNTs-modified resin decreases by 34.34%. • The mechanism of MWCNTs enhancing resin's gas-barrier and mechanical properties is explained. [ABSTRACT FROM AUTHOR]

The effects of grafting level of polyethylene glycol (PEG) grafted styrene ethylene propylene styrene (SEPS) on the intrinsic brittleness of epoxy thermosets were studied. The SEPS‐g‐PEG block copolymer (BCP) was synthesized by grafting various grafting degree of PEG (i.e., 10%, 20%, 30%, and 40%) on polystyrene (PS) blocks of SEPS following Williamson ether synthesis method. A total of 10 wt% of the BCP modifiers were dispersed in epoxy thermosets. PEG side chains were miscible in the epoxy which formed a uniform BCP dispersion within the epoxy thermoset matrix. As the degree of PEG grafting was increased, the BCP phase was absorbed in the epoxy matrix. This absorption occurred because the increase in PEG grafting provided more miscible PEG chains to bind the BCP and epoxy nanostructures together. The differential scanning calorimeter and dynamic mechanical thermal analysis analyses indicated that BCP toughened epoxy exhibited an improved glass transition temperature (Tg). At a 40% PEG grafting degree in the BCP, the critical stress intensity factor (KIC) and critical strain energy release rate (GIC) increased up to 80% and 180%, respectively. This trend suggested that the energy associated with fractures could be absorbed through the deformation of the softer phases when a load was applied to them. [ABSTRACT FROM AUTHOR]

A tetrafunctional glycidyl ether cyclic siloxane epoxy resin (TGTS) has been synthesized, characterized and cured with four aromatic amine hardeners: 1,3‐phenylenediamine (PDA), diethyltoluenediamine (DETDA), 4,4‐diaminodiphenylmethane (DDM) and 1,3‐bis(4‐aminophenoxy)benzene (APB). Each of the cured networks produces transparent and homogeneous networks, although when TGTS is cured with DETDA, reduced compatibility led to lower epoxide consumption, a more heterogenous microstructure and deleterious effects upon properties. Reduced miscibility of DETDA significantly impacts the chemical structure and microstructure of the network, resulting in significant reductions in thermal and mechanical properties but higher UV‐A transmission. The PDA‐, APB‐ and DDM‐cured networks conversely were more miscible and display properties typical of organic–inorganic hybrid networks, such as good mechanical properties at ambient and sub‐ambient temperatures, comparatively high glass transition temperatures, improved resistance to oxidation and lower UV‐A transmission. © 2024 The Author(s). Polymer International published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

This study is aimed at developing a fibre-reinforced polymer composite with a high bio-based content and to investigate its mechanical properties. A novel basalt fibre-reinforced polymer (BFRP) composite with bio-based matrix modified with different contents of star-like n-butyl methacrylate (n-BMA) block glycidyl methacrylate (GMA) copolymer has been developed. n-BMA blocks have flexible butyl units, while the epoxide group of GMA makes it miscible with the epoxy resin and is involved in the crosslinking network. The effect of the star-like polymer on the rheological behaviour of the epoxy was studied. The viscosity of the epoxy increased with increase in star-like polymer content. Tensile tests showed no noteworthy influence of star-like polymer on tensile properties. The addition of 0.5 wt.% star-like polymer increased the glass transition temperature by 8.2 °C. Mode-I interlaminar fracture toughness and low-velocity impact tests were performed on star-like polymer-modified BFRP laminates, where interfacial adhesion and impact energy capabilities were observed. Interlaminar fracture toughness improved by 45% and energy absorption capability increased threefold for BFRP laminates modified with 1 wt.% of star-like polymer when compared to unmodified BFRP laminates. This improvement could be attributed to the increase in ductility of the matrix on the addition of the star-like polymer, increasing resistance to impact and damage. Furthermore, scanning electron microscopy confirmed that with increase in star-like polymer content, the interfacial adhesion between the matrix and fibres improves. [ABSTRACT FROM AUTHOR]

Diglycidyl ether of bisphenol A crosslinking with glutaric anhydride is used to form the conventional “covalent adaptive network”, polyether sulfone (PES) by coiling and aggregating on the adaptive network is used to significantly increase the uncured resin viscosity for improving the processability of epoxy resin, but inevitably affecting the curing reaction and dynamic transesterification reaction. This study investigates the crucial roles of PES in curing dynamics and stress relaxation behavior. The results indicate that although PES does not directly participate in the crosslinking reaction of polyester‐based epoxy vitrimers. Moreover, the isothermal curing studies reveal that the addition of PES can greatly bring forward the reaction rate peak from conversion α = 0.6 to α = 0.2, meaning that the curing mechanism transfers from chemical control to diffusion control. Dynamic property analysis shows that the addition of PES significantly accelerates stress relaxation, especially at lower temperatures, leading to low viscous flow activation energy Eτ and relatively insensitive stress relaxation behavior to temperature. Introducing PES into vitrimer resin greatly improves crosslinking density (2.31 × 10⁴ mol m−3), enhancing glass transition temperature (82.68 °C), tensile strength (68.66 MPa), and fracture toughness (6.25%). Additionally, the modified vitrimer resin exhibits satisfying shape memory performance and reprocessing capability. [ABSTRACT FROM AUTHOR]

This paper reports polymer composites′ microstructure and dielectric properties based on an epoxy resin matrix containing different amounts (from 2–10 wt. %) of barium strontium titanate nanoparticles. (Ba,Sr)TiO3 was prepared using the hydrothermal method, showing an average particle size of 100 nm. The composites′ thermal properties and morphology were characterized using thermogravimetric analysis, differential scanning calorimetry, and scanning electron microscopy. Our studies show that the (Ba,Sr)TiO3 nanoparticles were well dispersed in the epoxy resin matrix thanks to controlled silane functionalization. Accordingly, the glass transition temperature (Tg) value of the nanocomposites was found to be 159.0 °C at 10 wt. % (Ba,Sr)TiO3 loading and is higher than the neat epoxy resin Tg (Tg=154.7 °C). Moreover, the dielectric composite properties were investigated comprehensively via a wide range of frequencies from 10 Hz to 100 kHz. The results indicate that (Ba,Sr)TiO3 nanopowders and the surface modifying filler play a crucial role in the significant increase of the dielectric constants, approximately 1.5 times at the optimum added amount (Ba,Sr)TiO3. The limited functionalization of (Ba,Sr)TiO3 nanoparticles by the silane affords to control the nanocomposite dielectric loss. Furthermore, the nanocomposites also exhibited good thermal stability. [ABSTRACT FROM AUTHOR]

Reducing the dependence of epoxy resin preparation on petroleum resources and developing thermosetting epoxy resins with excellent comprehensive performance are important directions for the current development of epoxy resins. This article uses biomass resource magnolol as the main raw material to prepare magnolol epoxy monomer (DGEM). Then, using 4,4-diaminodiphenylmethane (DDM) as the curing agent, the DGEM and bisphenol A epoxy resin (E44) were blended and cured. The results showed a dual modification effect of DGEM on the toughening and strengthening of E44 epoxy resin. When the mass ratio of DGEM to E44 is 30:70, the bending strength of the cured blended resin is 18.7% higher than that of the E44 system, and the tensile strength is 57.7% higher. When the mass ratio of DGEM to E44 is 5:95, the cured blended resin exhibits the optimal impact strength (5.10 kJ/mol), which is 22.9% higher than the pure E44 system. However, the addition of DGEM reduced the glass transition temperature and crosslinking degree of the blended resin system. The addition of DGEM improves the heat resistance and flame retardancy of the blended resin. When the mass ratio of DGEM: E44 was 50:50, the vertical combustion reached UL-94 V-0 level. [ABSTRACT FROM AUTHOR]

The disadvantage of poor thermal performance of epoxy resin limits its application in special fields, therefore we improve the thermal performance of epoxy resin by copolymerizing it with phthalonitrile resin. A novel self-promoted curing phthalonitrile monomer containing pyridine rings and amino groups (APNH) was successfully synthesized using 2-amino-4-hydroxypyridine and 4-nitrophthalonitril, and characterized by FTIR and NMR spectra. DSC confirmed that the APNH monomer exhibits curing behavior that is self-promoting. Copolymerizing the APNH monomer with epoxy resin enhances the thermal performance of the epoxy resin. The curing behavior of the EPNH copolymer was studied using DSC, which revealed two distinct curing peaks. FTIR analysis showed that the EPNH copolymer has formed structures such as triazine, phthalocyanine, and isoindoline. The presence of cyano groups significantly enhances the thermal properties of the copolymer, surpassing those of traditional epoxy resins. This enhancement in thermal performance amplifies with an increase in the content of the APNH monomer. The research indicates that the EPNH copolymer exhibits superior thermal stability and elevated glass transition temperatures, facilitating the application of epoxy resin in specialized areas. [ABSTRACT FROM AUTHOR]

This research focuses on the mechanical characterization of FG material graded with Graphene nano-platelets (GPLs) in the transverse direction. Different weight percentages of GPL (0–2 wt. %) were incorporated into epoxy resin for manufacturing the FGM using a simple casting method and the effects were analyzed. This paper aims to enhance the material’s performance, especially focusing on its potential use in biomedical tools. Mechanical tests including assessment on tensile, flexural, impact strength, and microhardness demonstrated substantial improvement in strength and stiffness as compared to other nanocomposite structures. Microstructural analysis using scanning electron microscopy (SEM), Fourier-Transform Infrared Spectroscopy (FTIR), and X-ray Diffraction (XRD) analysis which hint at the strong chemical interaction and physical association of GPL nanofiller with the epoxy resin. Thermal analysis was conducted using the Dynamic Mechanical Analysis (DMA) test, which revealed enhanced thermal stability of the FG specimen with a higher glass transition temperature than other carbon nanofillers mixed in epoxy resin. This is advantageous for the FG material to maintain its glassy state, maintaining safety and reliability during high-temperature medical applications. All these findings indicate that the proposed FG-GPL material possesses the necessary mechanical properties, suggesting that customized nanofiller integration could lead to significant advancements in medical procedures, such as in vivo stomach biopsy treatments, drug delivery systems, etc. The material also meets specific anatomical requirements and reduces the risk of malfunction, thereby ensuring patient safety as justified by current experimental investigations. [ABSTRACT FROM AUTHOR]

A phosphorus-containing compound, (oxybis(4,1-phenylene))bis(phenylphosphine oxide) (ODDPO), was successfully synthesized and used as a flame retardant for epoxy resin (EP). The results demonstrated that EP/ODDPO, containing 1.2 wt% phosphorus, achieved a vertical burning V-0 rating, with a limited oxygen index value of 29.2%, indicating excellent flame retardancy. Comprehensive evaluations revealed that ODDPO exhibited both gas-phase and condensed-phase flame-retardant effects on EP, with a particularly notable barrier effect. In addition, the incorporation of ODDPO had a minimal negative impact on the glass transition temperature (Tg) and thermal stability of the EP matrix. Compared to unmodified EP (EP-0), the Tg value and initial decomposition temperature of EP/ODDPO-1.2 decreased by only 7.6 °C and 10.0 °C, respectively. Moreover, the introduction of ODDPO significantly improved the hydrophobicity and water absorption resistance of epoxy materials, which is attributed to ODDPO's rigidity and symmetric structure, reducing water molecule permeation. Furthermore, the dielectric properties of ODDPO-modified EP samples were strengthened compared to EP-0, due to the ODDPO's symmetric structure reducing the polarity of the matrix. The above results indicated that ODDPO serves as an excellent flame retardant while enhancing other properties of the EP matrix, thereby contributing to the preparation and application of high-performance epoxy materials. [ABSTRACT FROM AUTHOR]

[Display omitted] Electroactive coatings for smart wearable textiles based on a furan bio-epoxy monomer (BOMF) crosslinked with isophorone diamine (IPD) and additivated with carbon nanotubes (CNTs) are reported herein. The effect of BOMF/IPD molar ratio on the curing reaction, as well as on the properties of the crosslinked resins was first assessed, and it was found that 1.5:1 BOMF/IPD molar ratio provided higher heat of reaction, glass transition temperature, and mechanical performance. The resin was then modified with CNT to prepare electrically conductive nanocomposite films, which exhibited conductivity values increased by eight orders of magnitude upon addition of 5 phr of CNTs. The epoxy/CNT nanocomposites were finally applied as coatings onto a cotton fabric to develop electrically conductive, hydrophobic and breathable textiles. Notably, the integration of CNTs imparted efficient and reversible electrothermal behavior to the cotton fabric, showcasing its potential application in smart and comfortable wearable electronic devices. [ABSTRACT FROM AUTHOR]

Highlights The bonding interface of carbon‐fiber‐reinforced polymer (CFRP)‐reinforced steel structure is a weak part, and nanomaterial‐modified adhesives are expected to improve its comprehensive performance. This paper investigates the micro‐modification mechanisms of nanomaterials on epoxy resin adhesives using molecular dynamics simulation method. It explores how the functionalized nano SiO2 and carbon nanotubes affects the thermal and mechanical properties of the epoxy resin adhesive. The models established using Materials Studio software include the pure epoxy resin adhesive model (EP) with varying degrees of crosslinking, the functionalized nano‐SiO2‐modified epoxy resin adhesive model (EP + SiO2/OH), the single‐walled carbon nanotube‐modified epoxy resin adhesive model (EP + SWNT), and the synergistic enhancements model of the epoxy resin adhesive with nano‐SiO2 and carbon nanotubes (EP + SWNT + SiO2/OH). Based on the aforementioned models, the Forcite module is used to calculate the free volume, glass transition temperature and mechanical properties of the adhesive. The results show that the degree of crosslinking effects significantly the mechanical performance of epoxy resin adhesive. A high degree of crosslinking restricts the movement of the molecular chain, enhancing the strength of the epoxy resin adhesive. Furthermore, the trend of the mechanical and thermal properties of the four models remains constant with the rise of temperature, and the properties decrease most significantly in the range of the glass transition temperature. Moreover, the epoxy resin adhesive doped with nanomaterials exhibits varying degrees of enhancement in mechanical and thermal properties. The epoxy resin adhesive reinforced with functionalized nano‐SiO2 and carbon nanotubes exhibits better properties compared to those with a single nanomaterial. The micro‐modification mechanism is revealed for nanomaterial modified epoxy resin adhesive. The degree of crosslinking effects significantly the mechanical performance of epoxy resin adhesive. The epoxy resin adhesive doped with nanomaterials exhibits varying degrees of enhancement in mechanical and thermal properties. [ABSTRACT FROM AUTHOR]

The bisphenol A-type phthalonitrile (BAPH) was blended with the classic epoxy system E51/DDS to prepare the epoxy/phthalonitrile thermoset. The curing kinetics were investigated by differential scanning calorimetry (DSC) using the isoconversional principle, and the average activation energy (Eα) of the E51/DDS curing reaction was found to decrease from 87 kJ/mol to 68.6 kJ/mol. Combining the results of the rheological study, the promoting effect of phthalonitrile on the crosslink of epoxy/amine is confirmed. The curing reaction of the blended resin was characterized using FTIR, and the results showed that BAPH could react with DDS. The thermal behaviors of the thermosets were investigated via DMA and TGA. The glass transition temperature (Tg) is found to increase from 181 °C to 195 °C. The char yield increases from 16% to 59.6% at 800 °C in a N2 atmosphere, which is higher than the calculated value based on the proportional principle. The AFM phase images show that there is no phase separation in the cured thermoset. The results imply that the cured epoxy/amine/phthalonitrile blend is probably a kind of copolymer. The real-time TG-MS indicated that the pyrolysis of the thermoset can be divided into two relatively independent stages, which can be assigned to the cleavage of the E51/DDS network, and the phthalocyanine/triazine/isoindoline, respectively. [ABSTRACT FROM AUTHOR]

This study aims to analyze the degradation behavior and mechanisms of amine-cured epoxy asphalt (EA) under the combined effects of ultraviolet (UV) radiation, oxygen, and temperature. To achieve this, amine-cured epoxy resin (ER) and EAs containing 35%, 45%, and 55% asphalt content were prepared and subjected to simulated UV-based aging. Various analytical techniques were employed to investigate the mechanical properties, microstructure, morphology, and oxidation layer of ER and EAs. The results indicate that after UV-based aging, ER and EAs with 35%–45% asphalt content experienced an increase in mass, a decrease in strength and glass transition temperature. In comparison, EAs with 55% asphalt content exhibited the opposite trends. The elongation and (Tanδ)max of ER and EAs reduced, whereas the storage modulus and hardness at mid to high temperatures rose. At the microstructural level, the degradation of the resin phase was confirmed by changes in ether, ester, and amide groups, whereas the generation of sulfoxide groups was associated with the oxidation of the asphalt phase. Compared with ER, the surface of EA has obvious defects after aging, which is the main reason for the decrease in contact angle. As the asphalt content increases, EAs exhibit higher carbonyl concentration, more profound oxidation, and more obvious performance degradation. This trend suggests that the resin phase mitigates the aging of the asphalt phase by absorbing harmful UV radiation and oxygen. [ABSTRACT FROM AUTHOR]

By combination of UV curing and frontal polymerization, interpenetrating polymer networks (IPNs) based on diglycidyl ether of bisphenol‐A (DGEBA) epoxy resin and polydicyclopentadiene (PDCPD) were prepared by UV‐induced simultaneously frontal polymerization in this paper. Compared with the net DGEBA cured polymer, the tensile strength, elongation at break and impact strength of the IPNs were simultaneously improved. The maximum tensile strength and elongation at break of the IPNs reached 100 MPa and 4.64%, respectively, and the maximum impact strength reached 7.34KJ/m2 with an improvement of 115.2% over that of the net DGEBA cured polymer. Thermogravimetric analysis (TGA) results revealed that the IPNs could enhance the thermal stability. Data of the differential scanning calorimetry (DSC) and TGA testing shows that the IPN shows a single glass transition temperature (Tg) which is between the Tg of DGEBA and DCPD, indicating homogeneous phase and highly cross‐linked IPN formed. Morphologies and molecular structure of the IPNs polymer were observed by scanning electron microscope (SEM) and characterized by Fourier transform infrared spectroscopy (FTIR), respectively, whose results also proved the formation of ideal IPNs structures. [ABSTRACT FROM AUTHOR]

Carbon fiber-epoxy laminates are used in aerospace manufacturing, e.g. as substrates for solar cells of satellites. Commonly, fibers or fibermats are impregnated with epoxy resin and placed in the required orientation. During subsequent curing, the resin molecules are crosslinked. Cured parts are characterized by their glass transition temperature (Tg). It has been observed that Tg of epoxy matrix resin vary with recorded absolute air humidity during wet fiber placement manufacturing. Based on the production data of a series production of 203 carbon fiber laminates for space application, an empirical linear relationship between the absolute air humidity at the beginning of each production day and the observed glass transition temperature of the fully cured laminate is formulated and validated. The empirical equation describes a linear decrease of achievable glass transition temperature with increasing absolute air humidity. The quantitative nature of the results encourages straightforward practical application to determine the maximum achievable Tg for given production conditions. [ABSTRACT FROM AUTHOR]

Fiber reinforced polymer composite structures are particularly vulnerable to high temperatures as their strength drastically reduces under elevated temperature conditions. Therefore, it is important to improve the thermal stability of such composite structures to expand their potential range of applications. In this study, the effect of mixing two epoxy monomers, DGEBA and Tactix 742, which are di‐ and tri‐functional, respectively, on the thermal stability of their composites is investigated. The thermo‐mechanical analysis of these composites revealed that the glass transition temperature rose from 123 to 229°C when Tactix 742 is increased from 25% to 75%. The thermal resistance property is attributed to a three‐dimensional crosslink network which is initiated by tri‐functional Tactix 742. However, the higher percentage of Tactix led to a reduction in strength, possibly due to decreased crystallinity and formed amorphous phase material. Subsequently, a tensile strength model was employed to assess the performance at elevated temperatures. It was shown that a matrix with a mix of di‐ and tri‐functional monomers is highly promising for manufacturing thermoresistant polymeric composites with robust mechanical properties, thereby expanding their potential applications across various engineering fields such as civil and construction industries. Highlights: A thermoresistant matrix by blending di‐ and tri‐functional epoxy monomers.Improved thermo‐mechanical properties and increased glass transition temperature of fiber reinforced composites.Mechanical performance of carbon fiber reinforced composites at elevated temperatures.Validated a model to estimate the tensile strengths of the composites at elevated temperatures. [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]

External plasticization is one of the effective ways to toughen epoxy resins. In this study, an inorganic filler (EMD) was prepared by chemical modification of diatomite and was used to fill epoxy resin matrix. The effects of different amounts (5%, 10%, 15%, and 20%) of raw diatomite (RD) and modified‐diatomite (EMD) on the mechanical and thermal properties of epoxy resin composites were studied. The mechanical results showed that the impact strength, tensile strength, and bending strength of EMD/EP were higher than those of RD/EP. The impact strength of EMD‐15/EP reached 5.39 KJ/m2, which was 36.8% higher than that of RD‐15/EP. Thermogravimetric analysis showed that the thermal stability of EMD/EP was better than that of RD/EP. The results of DMA show that the glass transition temperature of EMD/EP was lower than that of RD/EP. Non‐isothermal differential scanning calorimetry study showed that the apparent activation energy of EMD‐15/EP was much lower than that of RD‐15/EP, which proved that EMD could promote the curing of epoxy resin. The Malek method was used to determine that both the RD‐15/EP and EMD‐15/EP curing systems were autocatalytic (Šesták–Berggren) models. [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]

Highlights In this work, silicone polymer (PSOL)/glass fiber (GF)/epoxy (EP) composites were prepared by employing PSOL as interfacial modifier into GF/EP composites. The mechanical and dynamic mechanical properties of the composites were investigated to determine the optimal PSOL content. The effect of PSOL on the wettability of EP on GF was investigated. The micromorphology of the GF/EP composites was also examined by scanning electron microscope. The results demonstrate that the interfacial bonding between GF and epoxy resin was improved significantly by the addition of PSOL. Specifically, the interlaminar shear strength, tensile strength, elongation at break, and blending strength of the PSOL/GF/EP composites increased by 9.28%, 13.61%, 12.66%, and 19.22%, respectively. Moreover, the original thermal stability of the composites was improved by the incorporation of PSOL. This study highlights the effectiveness of PSOL as an interfacial modifier, enhancing the overall performance of GF/EP composites while improving their thermal stability. Silicone polymer (PSOL)/glass fiber (GF)/epoxy (EP) composite material is made of glass fiber and epoxy resin by hand paste molding. Silicon polymers as interface modifiers can improve the interface between glass fiber and epoxy resin. PSOL/GF/EP composites have good mechanical properties. The glass transition temperature of GF/EP composites was increased by silicon polymer. [ABSTRACT FROM AUTHOR]

Carbon nanotubes (CNT) is an ideal candidate for reinforced epoxy vitrimer composites, however, achieving a desirable improvement of the mechanical properties is a great challenge owing to CNT is extremely easy to aggregate. In this study, well‐dispersed CNT reinforced epoxy vitrimers, namely EVD/CNT, were prepared by combining ultrasonic dispersion and dynamic crosslinking techniques, using multiple wall carbon nanotube as reinforcement filler, sebacic acid as curing agent, diglycidyl ether of bisphenol A (DGEBA) as epoxy monomer, zinc acetylacetonate as transesterification catalyst, torque rheometer (internal mixer) as dynamic crosslinking equipment. The CNT reinforced epoxy vitrimers, namely EVS/CNT, were prepared using traditional static curing method. The structure and morphology, mechanical properties and stress relaxation behavior of EVS/CNT and EVD/CNT were comparatively investigated, and the influence of CNT content on the structure and properties of EVD/CNT prepared by dynamic crosslinking method were also studied. The results indicated that dynamic crosslinking technology can stably disperse CNT into epoxy vitrimer resin matrix under continuous shear force. However, CNT experienced severe secondary agglomeration during the static curing process. When the loading amount of CNT was 2 wt%, the tensile strength and elongation at break of EVD/CNT‐2 were 3.2 times and 2.2 times higher than those of EVS/CNT‐2, respectively. The Young's modulus and glass transition temperature (Tg) of EVD/CNT‐2 (6.43 ± 1.10 MPa, 29.6°C) were also higher than those of EVS/CNT‐2 (5.46 ± 0.31 MPa, 25.4°C). Moreover, dynamic crosslinking technology greatly shortened the reaction time of CNT reinforced epoxy vitrimers, improved production efficiency and reduced reaction energy consumption, and was expected to be used for large‐scale and industrial production. [ABSTRACT FROM AUTHOR]

Toughening the petroleum-based epoxy resin blends with bio-based modifiers without compromising their modulus, mechanical strength, and other properties is still a big challenge in view of the sustainability. In this study, a bio-based liquid crystal epoxy resin (THMT-EP) with an s-triazine ring structure was utilized to modify a petroleum-based bisphenol A epoxy resin (E51) with 4,4′-diaminodiphenylsulfone (DDS) as a curing agent, and the blended systems were evaluated for their thermal stability, mechanical properties, and flame retardancy. The results showed that the impact strength of the blended system initially increased and then decreased with the increase in THMT-EP content, and it reached the a maximum value of 26.5 kJ/m2 when the THMT-EP content was 5%, which was 31.2% higher than that of E51/DDS. Notably, the flexural strength, modulus, and glass transition temperature of the blended system were all simultaneously improved with the addition of THMT-EP. At the same time, the addition of THMT-EP enhanced the flame retardancy of the system by increasing the char yield at 700 °C and decreasing the peak heat release rate and total heat release rate. This work paves the way for a more sustainable improvement in the comprehensive performance of epoxy resin. [ABSTRACT FROM AUTHOR]

In this paper, the properties of T700 carbon fiber/epoxy resin matrix composites with pore damage were studied after aging in salt solution with different concentration, time and temperature, and the failure mechanism was analyzed. The mass change, SEM microstructure, glass transition temperature, infrared spectrum analysis and open hole tensile properties of the samples were analyzed after soaking in salt solution. The results show that the concentration of the salt solution has little effect on the properties of the material, while the aging time and temperature of the salt solution have more obvious effect on it. With the increase of temperature and time, the faster the moisture absorption rate, the greater the decrease of the glass transition temperature, the more serious the damage of the specimen morphology, the damage of the interface between the fiber and the matrix, and the open hole tensile strength. [ABSTRACT FROM AUTHOR]

Highlights The homogeneous dispersion of multi‐walled carbon nanotubes (MWCNTs) in a polymer matrix significantly affects the overall properties of composites. In this study, MWCNTs/epoxy (EP) composites were prepared using DeoxyriboNucleic acid (DNA) as a dispersant. The MWCNTs were uniformly dispersed in a phenalkamine curing agent and crosslinked with an epoxy resin matrix. The non‐covalent functionalization of DNA‐dispersed MWCNTs was confirmed by characterizing both the pristine and DNA‐modified MWCNTs. Additionally, the dispersion state and stability of MWCNTs in the curing agent solution were evaluated. Tensile strength and single‐lap‐shear (SLS) were employed to assess the mechanical properties of the composites. The results indicated that the DNA‐dispersed MWCNTs composites exhibited superior strength and toughness, with tensile and shear strengths of 46.81 and 19.64 MPa, respectively, at optimal ratios. These values represent increases of 68.38% and 50.96% compared to pure EP. Dynamic mechanical thermal analysis (DMTA) revealed that the energy storage modulus of DNA‐dispersed MWCNTs/EP composites increased to 2722 MPa, a 24.7% enhancement over pure EP. Furthermore, the thermal properties of the composites were thoroughly investigated. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) showed that the initial decomposition temperature of the DNA‐assisted dispersed composites rose to 330°C. The macromolecular relaxation of the EP materials occurred at higher temperatures, leading to an increased glass transition temperature. DNA was used to disperse MWCNTs in phenalkamine curing agent. MWCNTs/EP composites were made by crosslinking DNA‐dispersed MWCNTs with epoxy resin. DNA‐dispersed MWCNTs boosted tensile and lap shear strength. Thermal properties improved due to DNA‐dispersed MWCNTs, and increased the energy storage modulus of the composite. [ABSTRACT FROM AUTHOR]

Self‐healing polymers have been developed to improve durability and reduce costs associated with maintenance during service. The addition of thermoplastics to thermosets to produce mendable polymers appears as a promising self‐healing technique. In this study, poly (ethylene‐co‐methacrylic acid) (EMAA) was added to epoxy resin and the effects of EMAA addition on epoxy properties were evaluated. Specimens with two different contents of thermoplastic and particles sizes were manufactured. A two‐level full factorial experimental design was used to evaluate the effect of particle size and particle content on properties of epoxy modified with addition of EMAA. Tensile tests and dynamic mechanical analysis (DMA) were used and the evaluated responses were tensile strength, modulus of elasticity, and glass transition temperature (Tg). X‐ray computed tomography (XCT) was used to investigate particle size and concentration after manufacturing. It was found that the particle concentration has greater effects on stress–strain behavior of epoxy while Tg was not significantly affected by neither of the analyzed entrance variables. [ABSTRACT FROM AUTHOR]

The development of soft and biocompatible actuators is a current challenge in the fast‐growing field of soft robotics. A variety of shape‐memory and thermal actuators are currently being explored for application in these areas, especially to produce actuators that can operate at biocompatible temperatures for in vivo applications. Here we detail the synthesis of epoxy based materials, a class of materials not fully explored for soft actuators. By careful tuning of polymer composition by variation of monomer feed ratios, we show tuneable glass transition temperatures (Tgs) of these materials. Ambient temperature (30–60 °C) thermal actuators were then realised by casting of bilayers of epoxy resins with varying Tgs. Differences in thermal expansion when the Tg was reached lead to actuation in a specific direction. With optimisation, actuation in both the external‐heated and joule‐heated NiChrome‐epoxy actuators were able to occur at physiological temperatures (36–40 °C), previously unreported in the literature. For the joule‐heated NiChrome–epoxy actuators surface temperatures remained under 40 °C during actuation at low operating voltages (<2 V). Higher force and power output could be achieved in a repeatable fashion at higher driving voltages without loss of displacement, but also leading to higher surface temperatures. These materials and the actuation approach present an exciting opportunity to develop future implantable actuators to solve significant challenges related to quality of life and an ageing population. [ABSTRACT FROM AUTHOR]

Composite materials made of bio-based matrices reinforced with natural fibers are a potential solution to meet the environmental constraints of manufacturing industries. Interactions between a partially bio-based epoxy resin and flax fibers were investigated in three different ways. An internally developed experiment named Curing Thermal Monitoring (CTM) revealed that curing of epoxy–amine composite plates is accelerated by a factor 2 when reinforced by flax fibers containing 10% wt water. Deeper insight obtained using differential scanning calorimetry (DSC) revealed that the curing acceleration effect of water increases the variation of entropy and lead to higher activation energy values (Eα ≈ 55 kJ/mol). Dynamic mechanical analysis (DMA) measurements highlight that composite with wet fibers has a higher glass transition temperature (Tg = 60 °C) value after manufacturing, which is a consequence of the higher reactivity induced by water. By contrast, composite reinforced by dried flax fibers showed a lower curing reactivity and thus lower Eα values (≈ 43 kJ/mol) and Tg value (48 °C) after manufacturing. Both composites were stored under relative humidity conditions after manufacturing and evidenced an increase in Tg due to water absorption. A post-curing helped the composite with dried fibers to reach maximum Tg = (92 °C) while this was not the case for composite with wet fibers due to chaotic network geometry caused by the entropic effect (89 °C). Water contained in the flax fibers can act as a plasticizer after the post-curing as the Tg decreases with the absorbed water. This work gives a better understanding of the role of water naturally contained in flax fibers and point out the fact that monitoring the moisture of flax fibers is a key parameter to manufacture bio-based composites. [ABSTRACT FROM AUTHOR]

The performance and phase-separated microstructures of epoxy asphalt binders greatly depend on the concentration of epoxy resin or bitumen. In this paper, the effect of the epoxy resin (ER) concentration (10–90%) on the viscosity, thermo-mechanical properties, and phase-separated morphology of warm-mix epoxy asphalt binders (WEABs) was investigated using the Brookfield rotational viscometer, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and laser scanning confocal microscopy (LSCM). Due to the high reactivity of epoxy resin, the viscosity of WEABs increases with time. Furthermore, the initial viscosity of WEABs decreases with the ER concentration. Depending on the ER concentration, the viscosity–time behavior of WEABs is divided into three stages: slow (10–40%), fast (50–80%), and extremely slow (90%). In the slow stage, the viscosity slightly increases with the ER concentration, while the fast stage shows an opposite trend. DSC and DMA results reveal that WEABs with 10–80% ER exhibit two glass transition temperatures (Tgs) for cured epoxy resin and bitumen. Moreover, the Tgs of epoxy resin and bitumen increase with the ER concentration. However, WEAB with 90 % ER has only one Tg. LSCM observation shows that phase separation occurs in all WEABs. For WEABs containing 10–40% ER, spherical epoxy particles act as the discontinuous phase and disperse in the continuous bitumen phase. However, in WEABs with 50–90% ER, phase inversion takes place. Contrarily, bitumen particles disperse in the continuous epoxy phase. The damping properties of WEABs with the continuous epoxy phases increase with the ER concentration, while the crosslinking density shows an opposite trend. The occurrence of phase inversion results in a sharp increase in the tensile strength of WEABs. For WEABs with the continuous epoxy phases, the elongation at break increases with the ER concentration. The toughness first increases and then decreases with the ER concentration. A maximum toughness value shows at 70% ER. [ABSTRACT FROM AUTHOR]

A novel epoxy resin, DPHP, was synthesized from diphenolic acid, which contains biobased levulinic acid, with triethylphosphite, to improve the flame retardancy of bisphenol‐A diglycidyl ether (BADGE) epoxy. Curing experiments were conducted using isophorone diamine as a curing agent for BADGE and DPHP mixtures. Variations in cure kinetics, mechanical properties, and flame retardancy were evaluated across different DPHP contents. The introduction of phosphorus functional groups into DPHP affected the polarization of epoxide CO bonds, resulting in reduced apparent activation energy for epoxy curing reactions. However, the higher epoxy equivalent weight of DPHP compared with that of BADGE led to a decrease in the tensile strength and the glass transition temperature of the cured material with increasing DPHP content. A significant increase in char yield for combustion of the epoxy blend was observed, ranging from 8.3% at 0 wt% DPHP to 20.1% at 50 wt% DPHP. Additionally, cone calorimeter measurements showed significant reductions in heat release rate and total heat release, leading to a decrease in fire spread from 1.07 MJm−2 s−1 at 0 wt% DPHP to 0.43 MJm−2 s−1 at 50 wt% DPHP. These results show that the flame retardancy of the cured material improved significantly as the DPHP content increased. [ABSTRACT FROM AUTHOR]

Cellulose, a ubiquitous natural biopolymer, has diverse applications in industries such as paper manufacturing, textiles, and food. A pivotal breakthrough emerged with the discovery that ionic liquids (ILs) can dissolve cellulose, initiating comprehensive studies over the past two decades. This study explores the effectiveness of a selected system comprising [EMIM][OAc], [EMIM][DCA], and DMSO in cellulose dissolution, validated through a 5% cellulose solution, and the use of such systems as initiators of epoxy resin curing. In epoxy resin systems, the cellulose fibers formed in situ affect the mechanical properties of the final materials, which in the work presented here were flax fiber-reinforced epoxy composites. Differential Scanning Calorimetry (DSC) showed that cellulose inclusion minimally affected curing temperatures but reduced enthalpy. Scanning Electron Microscopy (SEM) demonstrated in situ cellulose fiber generation during mixing, ensuring high compatibility with the resin matrix. Mechanical testing revealed promising outcomes, including increased glass transition temperature (Tg) and enhanced Heat Deflection Temperature (HDT). However, a 50% reduction in impact strength indicated increased brittleness. [ABSTRACT FROM AUTHOR]

The systematic transfer of solvent‐free, additive flame retardant (FR) formulations from epoxy resins to glass fiber‐reinforced epoxy composites (GFRECs) through prepregs is difficult. Additionally, obtaining data on their post‐fire mechanics is often challenging. Utilizing melamine polyphosphate (MPP), ammonium polyphosphate (APP), and silane‐coated ammonium polyphosphate (SiAPP) FRs with low‐melting inorganic silicates (InSi) in an 8:2 proportion and 10% loading by weight in a diglycidyl ether of bisphenol A (DGEBA) resin, a systematic investigation of the processing properties, room‐temperature mechanics, and temperature‐based mechanics of the systems was performed. The resin was cured with a dicyandiamide hardener (DICY) and a urone accelerator. The results revealed no substantial impact of these FRs at the current loading on the resin's glass transition temperature or processability. However, the fire residues from cone calorimetry tests of the composites containing FRs were found to be only 15‐20% of the thickness of the resins, implying a suppression of intumescence upon transfer. At room temperature, the decrease in the flexural modulus for the composites containing FRs was negligible. Exposure of the composites in a furnace at 400°C as a preliminary study before ignition tests was shown to cause significant flexural moduli reductions after 2.5 min of exposure and complete delamination after 3 min making further testing unviable. This study emphasizes the need for future research on recovering modes of action upon transfer of FR formulations from resins to composites. Based on the challenges outlined in this investigation, sample adaptation methods for post‐fire analysis will be developed in a future study. Highlights: Processibility of resins for prepreg production unaffected by polyphosphate/inorganic silicate flame retardants (FRs).FR formulations had a negligible effect on the mechanics of the composites.15%–25% increase in the fracture toughness of the DGEBA‐based resin matrix with FRs.Suppression of intumescent behavior in the composites verified quantitatively.Significant reduction in flexural moduli of the composites post‐400°C exposure in a furnace. [ABSTRACT FROM AUTHOR]

This article explores the impact of Graphene Nanoplatelet (GNP) reinforcement on the mechanical and thermomechanical properties of epoxy adhesive. The impact of GNPs on the structural adhesive largely depends on factors like dispersion stability and GNP concentration. Given the complexity of these interactions, it is imperative to obtain indicators for the degree of each interaction. In this study, Pearson correlation matrix and heatmaps analysis were used to analyze the relationship between various variables and the strength of the connection. The addition of GNP at various concentrations to the epoxy adhesive led to a reduction in storage modulus, loss modulus, and glass transition temperature, attributed to the agglomeration of GNP. In bulk specimens, the incorporation of GNP, regardless of its content, has decreased tensile stress up to 70.7% while increasing its fracture elongation up to 396.3%. Within joining specimens with GNP, specimens with 1.5 wt% GNP content showed the highest cohesive fracture mode and largest shear strength. Pearson correlation matrix and heatmaps have demonstrated very good accuracy in reflecting the experimental data. They offer a comprehensive assessment of the relationship between various variables while indicating the degree of influence each variable has on the properties of the adhesive and joining specimens. Highlights: GNP effects in adhesive can be accurately analyzed with Pearson correlation matrix & heatmaps.Connections strength for various variables can be shown by Pearson correlation matrix & heatmaps.Pearson correlation matrix & heatmaps assess variable relationships comprehensively. [ABSTRACT FROM AUTHOR]

This research aims to highlight the importance of diverse forms of graphitic carbon nitride (g-C3N4) as strengthening elements in epoxy composites. It explores the influence of three different forms of g-C3N4 and their concentrations on the mechanical properties of the epoxy composites. Various characterization techniques, such as scanning electron microscopy (SEM), dynamic light scattering (DLS), thermogravimetric analysis (TGA), and Fourier-transform infrared spectroscopy (FTIR), were utilized to comprehend the effects of g-C3N4 morphology and particle size on the physical and chemical characteristics of epoxy resin. Mechanical properties, such as tensile strength, strain, modulus, and fracture toughness, were determined for the composite samples. SEM analysis was performed to examine crack morphology in samples with different reinforcements. Findings indicate that optimal mechanical properties were achieved with a 0.5 wt% bulk g-C3N4 filler, enhancing tensile strength by 14%. SEM micrographs of fracture surfaces revealed a transition from brittle to rough morphology, suggesting increased toughness in the composites. While the TGA results showed no significant impact on degradation temperature, dynamic mechanical analysis demonstrated a 17% increase in glass transition temperature. Furthermore, the improvement in thermal breakdown up to 600 °C was attributed to reinforced covalent bonds between carbon and nitrogen, supported by FTIR results. [ABSTRACT FROM AUTHOR]

Biochar (BC) is a by-product rich in carbon, from the pyrolysis of biomass, and therefore, it has great appeal to be used in several applications. In the present work, the use of biochar from poultry litter waste (PLW) as a filler for composites with epoxy resin is evaluated regarding its performance in the thermal, mechanical and dynamic mechanical properties. The BC was produced from the pyrolysis of the PLW, and the composites were produced from concentrations of 2.5, 5.0 and 10.0 wt% of BC, in relation to the epoxy resin mass. The composites were characterized in terms of micrography (MEV), infrared spectroscopy with Fourier transform (FTIR), thermogravimetric analysis (TGA), mechanical properties (tension and impact) and dynamic mechanical analysis (DMA). From the dynamic mechanical point of view, there was a considerable increase in parameters such as storage modulus at both glassy (≈ 23%) and rubbery regions (≈ 43%) and loss modulus (≈ 32%). However, a decrease at the glass transition temperature, in loss modulus, (≈ 19 °C) was reported, comparing the neat epoxy with those composites with 10 wt% of BC. This behavior was mainly related to the poor dispersion of BC into the composites, especially those with 10 wt% of reinforcement. [ABSTRACT FROM AUTHOR]

The current study deals with the fabrication of crosslinked epoxy composites reinforced with several loadings of aluminum nanorods (i.e., 5, 10, 15 and 20) wt% by a hand lay-up technique. Both pyromellitic dianhydride and glycerin utilized as cross-linker agents. The thermal, morphological and mechanical properties of the resultant composites were characterized as a function of nanorods content and type of cross-linker using a wide range of analytical and testing techniques. The results showed that using a combination of pyromellitic dianhydride and glycerin provide more adhesion efficiently between the nanorods and epoxy compared to the individual cross-linker. Also, the results demonstrated that both tensile and flexural strengths, and their moduli were increased with adding nanorods content up to 15 wt% followed by the moderate improvement. The maximum value of tensile, flexural strengths, tensile modulus and flexural modulus are ~ (6000, 96, 5000, 10,000) MPa, respectively; for crosslinked epoxy composites, which are higher than of pure epoxy by ~ (20, 37, 56, 53)%. Comparably, thermal degradation temperature (i.e., 300 °C) of the plain epoxy is shifted slightly toward higher temperature after the cross-linking reaction, which is likely due to a good interaction between epoxy molecules leads to an improvement in the thermal stability of the composite materials. In addition, both glass transition and melting temperatures of the crosslinked epoxy samples increased from by 37.6% and 11.7%, respectively. These results correlate with images from scanning electron microscopy, which showed less agglomeration and good distribution of nanorods particles into the crosslinked epoxy matrix. [ABSTRACT FROM AUTHOR]

The work represents the results of experimental research on the influence of the nanofiller’s nature on the thermal physical properties of composite materials. Polymer composite materials based on epoxy diane oligomer ED-20 were modified by 4-aminobenzoic acid. Martens yield temperature was researched and the glass transition temperature of the developed materials was determined. For the establishment of the thermal field’s effect on the structural processes of composite materials, the thermal coefficient of linear expansion of the materials was researched. Due to the necessity of studying the influence of temperature on physical-chemical processes and transformations in polymer composites, modern thermal analysis methods were used – differential thermal and thermal gravimetric analysis. Based on the analysis of experimental data, the optimal content of 4-aminobenzoic acid q  0.10 wt.% was determined per 100 wt.% of the ED-20 oligomer, which leads to the improvement of thermal physical properties of epoxy composite materials. [ABSTRACT FROM AUTHOR]

Experimental and molecular dynamics simulations were employed to investigate epoxy shape memory polymers' thermal‐mechanical properties and shape memory characteristics, utilizing polyether amine and modified hexanediamine as curing agents following the material prerequisites for variable stiffness fixtures. Glass transition temperature and Young's modulus of epoxy shape memory polymers are characterized by dynamic mechanical analysis. The consistency of the glass transition temperature between the simulation model and the experimental findings verified the accuracy of the molecular dynamics simulation. The uniaxial tensile simulation revealed that non‐bond energy predominantly exerts its influence in stretch. After reaching the yield stress, the weight fraction of the curing agent affects the generation of internal pores, with the yield stress of systems exhibiting substantial pores being minor. Systems characterized by a higher weight fraction of curing agents are more prone to pore formulation. Simulation of shape memory properties demonstrates that the entropy resulting from differences in molecular weight impacts the simulated system's shape fixation ratio and shape recovery ratio. [ABSTRACT FROM AUTHOR]

The curing shrinkage of epoxy resin can generate residual strains and internal stresses that reduce the material's strength and life. In this paper, a thermocouple‐compensated fiber grating detection method for the gel time and residual strain in epoxy resin is proposed. The strain evolution and glass transition temperature of E51/W93 epoxy systems with different Al2O3 contents cured at 30°C are detected by fiber Bragg gratings and DSC tests. The generation mechanism of residual strain in epoxy resin filled with Al2O3 fillers is studied. The gel time, gel temperature and residual strain of epoxy resin can be measured by this method. The results show that the cure shrinkage of epoxy is affected by chemical shrinkage, thermal expansion or shrinkage, and demolding, resulting in residual strain of the material after curing. Moreover, the glass mold has a great interference with the curing shrinkage of epoxy. The Al2O3 filler can prolong the gel time of E51/W93 epoxy systems, and reduce the exothermic peak temperature of curing. When the content of Al2O3 filler exceeds 44.44 wt.%, the low proportion of epoxy and the thermal conductivity of the filler make the curing shrinkage of epoxy during the heating stage mainly affected by chemical shrinkage. The glass transition temperature of the epoxy with Al2O3 content of 70.59 wt.% is the maximum, and the residual strain is at a low level. This method is helpful to analyze the curing shrinkage characteristics of materials, and is of great significance for evaluating the properties of epoxy cured products and guiding the optimization of material parameters. Highlights: A method for measuring the gel time and residual strain of curing in epoxy resin is proposed.The study focuses on the detection of key parameters during the curing of epoxy resins with different Al2O3 contents.The aim is to analyze the curing shrinkage and residual strain generation mechanism of epoxy resin filled with different contents of Al2O3. [ABSTRACT FROM AUTHOR]

Epoxy resins‐based engineering plastics are indispensable in the global economy, but they have created a serious waste crisis caused by their chemical cross‐linked networks. To solve this problem, current strategies often require the assistance of catalysts or solvents at the expense of thermal and mechanical performance. In this work, a high‐performance epoxy resin featuring dynamic ester and disulfide bonds (TDS) is reported, which exhibits higher thermal and mechanical properties than common engineering plastics, i.e., tensile strength and modulus of 66.6 MPa and 2.63 GPa, flexural strength and modulus of 103.2 MPa and 3.52 GPa, and glass transition temperature (Tg) of 133 °C. Moreover, the reversible transformation between aromatic disulfide bonds and thiyl radicals endows TDS epoxy resin with autonomous visualization of damage and healing. In addition, the harmonious interplay between disulfide and ester bonds‐promoted by tertiary amine accelerated the topological network rearrangements, enabling TDS to easily reshape and weld. Specifically, TDS can be completely degraded in pure water at 200 °C without any catalyst, and the degraded products can be directly re‐polymerized to achieve green closed‐loop recycling. This work proposes a simple and economical strategy for the development of epoxy resin‐based cutting‐edge engineering plastics that are both functional and sustainable. [ABSTRACT FROM AUTHOR]

Glycidyl ethers are prepared from a series of furan‐based diols and cured with a diamine to form thermosets. The furan diols demonstrate lower toxicity than bisphenol‐A in a prior study. The diglycidyl ethers show improved thermal stability compared to the parent diols. Cured thermosets are prepared at elevated temperature using isophorone diamine (IPDA). Glass transition temperatures are in the range of 30–54 °C and depend on the structure of the furan diol. Coatings are prepared on steel substrates and show very high hardness, good adhesion, and a range of flexibility. Properties compare favorably with a control based on a bisphenol‐A epoxy resin. The study demonstrates that epoxy resins based on furan diols, which have been shown to have lower toxicity than bisphenol‐A, can form thermosets having properties comparable to a standard epoxy resin system; and thus, are viable as replacements for bisphenol‐A epoxy resins. [ABSTRACT FROM AUTHOR]

Aligned with the prevailing sustainability paradigm, the imperative adoption of bio‐based substitutes for constituents within petroleum‐derived epoxy resin becomes evident. Blending bio‐based and petroleum‐based epoxy resins and curing agents, establishes a synergistic compromise addressing both sustainability imperatives and the mechanical efficacy of thermosets. The conventional approach to discovering optimal compositions for multi‐component mixtures under specific boundary conditions includes empirical trial and error and is seen as a protracted and inefficient endeavor. Conversely, leveraging machine learning might afford a streamlined and confident resolution to this challenge. This investigation elucidates the requisite strategies for maximizing the efficiency of material property optimization through the application of Bayesian optimization and active learning. Illustratively, the study demonstrates the proficient optimization of the glass transition temperature within a four‐component epoxy resin system. This optimization is conducted across varying ranges of bio‐content and cost considerations. The study underscores the utility of machine learning in achieving this task with notable efficiency. The efficacy of least squares, kernel ridge regression, Gaussian process regression, and artificial neural networks, is meticulously evaluated through comprehensive seven‐fold cross‐validation and validated against experimental data. [ABSTRACT FROM AUTHOR]

Functional cyclophosphazenes have proven to be effective modifiers of polymer materials, significantly improving their performance properties, such as adhesive characteristics, mechanical strength, thermal stability, fire resistance, etc. In this study, 4-(β-carboxyethenyl)phenoxy-phenoxycyclotriphosphazenes (CPPP) were obtained by the condensation of 4-formylphenoxy-phenoxycyclotriphosphazene with malonic acid. Its structure was studied using 31P, 1H, and 13C NMR spectroscopy and MALDI-TOF mass spectrometry, and the thermal properties were determined by DSC and TGA methods. Molecular modeling using the MM2 method showed that CPPPs are nanosized with diameters of spheres described around the molecules in the range of 1.34–1.93 nm, which allows them to be classified as nanosized structures. The epoxy resin DER-331 was cured with CPPP, and the conversion of epoxy groups was assessed using IR spectroscopy. Using optical interferometry, it was shown that CPPPs are well compatible with epoxy resin in the temperature range from 80 to 130 °C. It was established that the cured epoxy composition was fire resistant, as it successfully passed the UL-94 vertical combustion test due to the formation of porous coke during the combustion process and also had high heat resistance and thermal stability (decomposition onset temperature about 300 °C, glass transition temperature 230 °C). The composition has low water absorption, high resistance to fresh and salt water, fire resistance, and adhesive strength to steel and aluminum (11 ± 0.2 MPa), which makes it promising for use as an adhesive composition for gluing parts in the shipbuilding and automotive industries, the aviation industry, and radio electronics. [ABSTRACT FROM AUTHOR]