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In this paper, the gamma and neutron shielding behavior of chemically bonded high atomic number (Z), tungsten trioxide‐polyvinyl alcohol‐polyvinylpyrrolidone (PW), and bismuth oxide‐polyvinyl alcohol‐polyvinylpyrrolidone (PB) composites were reported at varying thickness. The PW and PB composites were prepared through the dissolution technique rather than the commonly used dispersion technique. The gamma and neutron attenuation characteristics of the composites were studied using 22Na (0.511 and 1.274 MeV energy) and 252Cf (0–10 MeV energy) sources, respectively. The half value layer of PW and PB composite was found to be 61.22 ± 0.914 mm and 48.29 ± 1.52 mm and the linear attenuation coefficient was found to be 0.115 and 0.144 cm−1 at 0.511 MeV, respectively. Further, the experimental gamma‐ray attenuation results were validated theoretically using Phy‐X software and found to be well in agreement with the experimental data. Both the composites also showed similar neutron shielding behavior when compared to the commercially used high‐density polyethylene (HDPE). The developed composites possess good mechanical properties as they did not show any cracks or wrinkles after undergoing 5400 bending cycles during the flex test, showing their high durability of flexibility. Thus, these composites are found to be suitable for shielding both, the gamma‐rays and neutrons. [ABSTRACT FROM AUTHOR]

This paper offers a thorough unfolding of the many contributions that water‐soluble polymers (WSPs) play in cementitious composites. The several forms of WSPs—natural, semi‐synthetic, and artificial—are examined, and their methods of action in cementitious composites are investigated. The topics of binding, association, adhesion, complexation, and bridge creation are covered in the literature. The effects of WSPs on the microstructure, freshness, mechanical properties, and durability of cement‐based goods are also investigated in this review. The advantages and disadvantages of utilizing WSPs in cement‐based products are also discussed. Following a detailed analysis of the most significant findings, recommendations are made for both academic and practical research areas and applications. This study provides useful information for both experts and novices by elucidating the multi‐applications of WSPs in cementitious materials. [ABSTRACT FROM AUTHOR]

The contradiction between the migration rate of molecular chains and mechanical strength has always been a key factor affecting the practical application of self‐healing anticorrosion coatings. In this paper, a series of supramolecular self‐healing elastomers (SPU‐MP) were prepared by the reaction of diphenylmethane diisocyanate and polyether amine. The results shown that the proportion of polyetheramine D230 (D230) in molecular segments affects the hydrogen bond density between molecular chains, thereby affecting the self‐healing efficiency and mechanical strength of SPU‐MP. When the ratio of D230 and polyetheramine D400 (D400) is 2:8, the tensile fracture strength of SPU‐MP8 is 5.08 MPa, and the self‐healing efficiency reaches 82.1% after 10 h of repair at room temperature. Further increasing the ratio of D230 increases the relaxation time of the molecular chain due to the increase in hydrogen bond density, resulting in a decrease in the self‐healing efficiency of SPU‐MP. The results of electrochemical experiments and neutral salt spray experiments indicate that the anticorrosion coating prepared by SPU‐MP8 exhibits good self‐healing performance. After immersing in 3.5 wt.% NaCl solution for 35 days, the low‐frequency impedance modulus of the intact coating and the scratch coating were both higher than 107 Ω cm2, still shown good anticorrosion ability. [ABSTRACT FROM AUTHOR]

Because of the significant advantages of bone adhesives compared with traditional mechanical fixation, many scholars have studied polyurethane bone adhesives. However, polyurethane will release a lot of heat in the reaction process, producing high temperature. The high temperature does not only easily cause a human discomfort but also will destroy the tissue structure of human. In this paper, a new polyurethane composite based on phase transition materials and hydroxyapatite is prepared to reduce released heat for application in bone binder. The mechanical properties, adhesive strength, and released heat‐induced temperature of polyurethane composite are investigated in detail. It exhibits good viscoelastic performance with a large elastic deformation (>30%) and good adhesive strength (>0.2 MPa). Furthermore, the released heat of polyurethane composite is effectively reduced, in which the temperature drastically decreases from 110.4 to 41.8°C. The work does not only confirm formation of high‐performance bone binder but also provides a new method to reduce released heat of polyurethane for various applications. [ABSTRACT FROM AUTHOR]

The problem of strength loss in electrically conductive composites made with dispersed fillers in the polymer binder is solved by spraying an aerosol of graphite on a textile material with a 3D weave of threads, or on knitwear of fibers with various structure and chemical composition. The loose microstructure of cotton fibers and the developed surface of elastic filaments made of synthetic polymers retain colloidal graphite particles in a layered composite during cyclic deformation. The electrical conductivity of knitwear with graphite changes during stretching due to the reversible displacement of graphite particles, first during straightening and then during stretching of elastic threads. The 130 ± 5 strain sensitivity GF and 12,000 ± 95 кPa−1 stress sensitivity QF of the composites presented in this paper exceed the corresponding parameters of known electrically conductive composites. The combination of a significant change in electrical conductivity with the elasticity of the developed knitwear‐based composite is important for the use in load cells, smart clothes, medical devices, and robotics. [ABSTRACT FROM AUTHOR]

The blending of different elastomers can greatly broaden the application range of rubber materials. However, due to the poor compatibility between polar elastomers and non‐polar elastomers, severe phase separation occurs during the blending process, which severely degrades their processing performance and mechanical properties. In this paper, we prepared SBR‐P/XNBR blends by emulsion blending polar modified styrene‐butadiene rubber (SBR‐P) latex with carboxylated nitrile rubber (XNBR) latex. The effects of the blending ratios on the vulcanization behavior, mechanical strength, dynamic mechanical properties, and oil resistance of the rubber compounds were studied. Experimental results showed that the mechanical strength and oil resistance of the modified SBR‐P/XNBR blends are significantly higher than the unmodified SBR and XNBR blends. The dynamic mechanical analysis curve results of the rubber compounds showed that SBR‐P has good compatibility with XNBR. With the increasing addition of XNBR, the oil resistance of the rubber compounds improves, and the solvent adsorption is reduced by over 60%.This study proposes a solution for utilizing non‐polar rubbers, which are typically not oil‐resistant, in oily environments. The proposed solution enables the preparation of composites with excellent mechanical properties in such environments. [ABSTRACT FROM AUTHOR]

The article titled "Correction to 'Study of the impact of epoxidized plant oil phospholipids and hydroxyl radicals on crosslinked epoxy resins'" in the Journal of Applied Polymer Science contains a correction regarding a figure description in section 3.5 of the paper. The corrected sentence clarifies that Figure 7 shows the proposed mechanism between ECO and EP resin, with Figure 7a illustrating the interaction of ECO-oxirane with EP causing a decrease in mechanical properties and thermal stability, and Figure 7b showing the interaction between ECO-phospholipids and EP causing flame retardant and highly reduced toxicity properties. The authors apologize for the error. [Extracted from the article]

Shrinking resources of fossil oil prompt search for other biosphere‐present substrates to obtain polyols, which in turn are basic components to synthesize polyurethane foams (PUF). Widely available examples are biopolymers like starch, cellulose, and chitosan. It has been shown that oligomeric chitosan as well as water soluble chitosan can be applied to obtain polyols and rigid PUF of good performance properties. In this paper, the higher molecular mass chitosans, insoluble in organic solvents and water, were converted to polyols and ultimately into foamed polyurethane plastics. The polyols were characterized by the infrared spectra (IR), 1H‐NMR, and MALDI‐ToF methods. Their properties, such as density, viscosity, surface tension and hydroxyl numbers, were determined. The PUF were obtained from these polyols of various molecular mass. The biodegradable, rigid PUF of enhanced thermal resistance were obtained. Their physical parameters like apparent density, water volume absorption, dimension stability, heat conductance, compressive strength, and heat resistance at 150 and 175°C were studied and compared with those synthesized previously from oligomeric chitosan and water soluble chitosan. [ABSTRACT FROM AUTHOR]

Sticking between the thermoplastic polymer and metal tool is a crucial issue, as it determines whether the manufactured part can be ejected from the metal mold. Polyimide (PI) release films have been widely used in the processing of fiber‐reinforced thermoplastic polymer composites. Compared with other release mediums such as release agents, PI release film has a higher release efficiency. However, the underlying release mechanism is still not well understood which is essential to improve their performance further and reduce the cost. In this paper, poly(ether ketone ketone) (PEKK) polymer was melted and cooled down between two PI films. The surface morphologies and chemical compositions of the PI film and PEKK were characterized both before and after release using atomic force microscope, x‐ray photoelectron spectroscopy, contact angle measurements, and confocal microscopy. It showed that a thin PI layer was transferred from the PI release film to the PEKK surface during the release process. Based on these experimental results, a modified boundary layer mechanism is proposed as a hypothesis to describe the release mechanism of PI films. Our results give a fundamental understanding of how PI film works for the release of thermoplastics with high processing temperatures and may help to improve the performance and reduce the costs of existing PI films and may give guidance to the design of new release media. [ABSTRACT FROM AUTHOR]

Pulverized coal (coal) possesses a layered structure similar to graphite and is a potential reinforcing filler. In this paper, ball milling is used to reduce the particle diameter of coal. The coal is modified with KH‐560 to obtain K‐COAL and prepared K‐COAL/styrene‐butadiene rubber (SBR) composites. In addition, carbon black (CB) is modified to obtain CB‐Si69, K‐COAL and CB‐Si69 are added to SBR in different ratios to prepare COAL/CB/SBR composites. The results show that the addition of K‐COAL can improve the vulcanization performance, thermal stability, and mechanical properties of SBR composites, but the reinforcing effect is weak. In the COAL/CB/SBR composites, the vulcanization and mechanical properties of the composites gradually increase with the increase of CB, while those of the thermal stability decrease. The tensile strength of the 10 phr COAL/30 phr CB/SBR composite is 24.1 MPa, which is elevated by 1105% and 205% compared with the pure SBR and 40 phr K‐COAL/SBR composites, respectively. The composites maintain high elasticity while the tensile strengths are greatly improved, and the mechanical properties are significantly enhanced. In conclusion, this paper provides a reference for the clean utilization of coal and shows new possibilities for finding new fillers to replace CB. [ABSTRACT FROM AUTHOR]

The type of matrix resin of the semi‐conductive shielding layer directly affects the thermal aging characteristics of the semi‐conductive shielding layer and the high‐voltage cable. In this paper, ethylene vinyl acetate (EVA), ethylene ethyl acrylate (EEA), and ethylene butyl acrylate (EBA) resins were used as matrix to prepare carbon black (CB) + EVA, CB + EEA, and CB + EBA shielding materials. The law of physicochemical, electrical, and mechanical properties of different matrix resin shielding materials with aging time was studied, and the influence mechanism of matrix resin on the aging characteristics of shielding materials was analyzed. The results show: with the increase of aging time, the crystallization area and the number of functional groups of the three shielding materials decreased to varying degrees. The number of functional groups in CB + EBA shielding materials decreased evenly with aging time, but that of CB + EVA and CB + EEA shielding materials changed significantly after 7 days of aging. After 60 days of aging, the crystallization area of CB + EBA shielding material changed slightly, but that of CB + EVA and CB + EEA shielding material decrease significantly. The electrical properties of the three shielding materials showed different decreasing trend with aging time. When the aging time is 7 days, the positive temperature coefficient (PTC) effect of CB + EEA shielding material decreases obviously. When the aging time is 30 days, the resistivity of CB + EVA and CB + EEA shielding material increases slowly (9 Ω cm–12 Ω cm) with the increase of temperature. When the aging time is 60 days, the resistivity of CB + EBA shielding material decreases obviously, and the PTC effect weakens obviously. Taking the mechanical properties of the shielding material as reference, the rapid deterioration stage of the mechanical properties of the three shielding materials is different. The CB + EVA and CB + EEA shielding material rapid deterioration time is 0–7 days, and the tensile strength and elongation of the shielding material are greatly reduced. The rapid deterioration stage of CB + EBA shielding material is 7–30 days, and the tensile strength and elongation decrease from 24.38 MPa and 499.5% to 14 MPa and 155.7%, respectively. This work can provide data support for the selection of matrix resin of shielding material and the fault analysis of shielding layer of high voltage cable. [ABSTRACT FROM AUTHOR]

A series of novel thermoplastic polyurethane elastomers with both low surface energy and antibacterial activity were synthesized in this paper. Firstly, four imidazole salt diols with different alkyl chain lengths at the N‐position of imidazolium cation ([CnIm+][Cl−]) were prepared. Then, imidazolium‐based ionic thermoplastic polyurethane elastomers (Si‐ITPUs) were formulated by incorporating polydimethylsiloxane and polytetramethylene glycol as a mixed soft segment, 1,4‐butanediol and [CnIm+][Cl−] as a chain extender, and 4,4′‐dicyclohexylmethane diisocyanate. The structure, thermal stability, mechanical properties, physical crosslinking density, and the anti‐graffiti properties of Si‐ITPUs were evaluated. The surface energy and water absorption were evaluated through static contact angle and water resistance tests, respectively. Furthermore, the antibacterial activities against both Staphylococcus.aureus and Escherichia coli were characterized by the plate colony counting method. The results demonstrated that Si‐ITPUs possessed surface energy of approximately 23 mN/m, which conferred excellent anti‐graffiti and self‐cleaning performance. Furthermore, the increase of the alkyl chain length of substitutions resulted in a decrease in the tensile strength but an increase in the elongation at break. Si‐ITPU‐C4 exhibited optimized antibacterial activities with an antibacterial rate of more than 99.9% against both S. aureus and E. coli. This novel polyurethane is anticipated to find applications in the medical device industry and food processing sector. [ABSTRACT FROM AUTHOR]

With the implementation of plastic restrictions and the increasingly serious problem of environmental pollution, paper with green and recyclable characteristics is gradually becoming a substitute for packaging materials. However, the rich cellulose structure in the paper, which contains hydroxyl groups leading to its hydrophilicity, allows water molecules to penetrate the paper and disrupt the hydrogen bonds between cellulose, resulting in a decrease in mechanical properties. Therefore, waterproof coatings are crucial for paper‐based materials to be used in many applications. Based on this, the paper surface was chemically modified with castor oil‐based resin (CO‐590) monomer prepared by coupling agent and castor oil (CO). The results indicated that the modified paper with the contact angle (CA) of 114° had excellent waterproof performance and had a reduction by 40.3% in water vapor transmission rate (WVTR), but also its mechanical increased to 26.9 MPa and the decomposition temperature to 410.5°C. In addition, the coating on its surface could be removed in an alkaline solution and had a possibility to recycle blank paper in the future for manufacturing sustainable production. This work not only provides a method for preparing modified packaging paper, but also expands the application fields of materials. [ABSTRACT FROM AUTHOR]

Polyurea (PUA) is widely used as a coating in construction, tunnels, bridges, and other fields because of its excellent performance. However, its combustion emits toxic gases and smoke, hindering escape and posing potential fatality risks. Enhancing the flame retardancy of PUA is crucial for safety and expanding its applications. The synthesis of two‐dimensional FePP nanosheets was reported in this paper, employing the solvothermal method, followed by the sequential growth of MoS2 and Ni‐MOF to establish a multilayer composite structure. The elemental composition and morphology of the synthesized FePP@MoS2@Ni‐MOF flame retardants were characterized and analyzed. The flame retardant properties of polyurea composites with varying amounts of FePP@MoS2@Ni‐MOF were investigated using Cone calorimeter tests. The results showed that the prepared flame retardant had good thermal stability and significantly improved fire safety properties. The PUA/FePP@MoS2@Ni‐MOF 3.0 composite exhibited notable improvements compared to pure PUA. Specifically, the peak heat release rate, total heat release rate and peak smoke production rate were reduced by 39.76%, 29.33% and 17.86%, respectively, while total smoke production and total CO production (COP) were reduced by 21.30% and 54.47%. This study provides new insights and experimental basis for the technological development of novel flame retardant coating materials. [ABSTRACT FROM AUTHOR]

This paper investigated the cross‐linking network structure of epoxy asphalt (EA) with the different ratio of composite curing agents, and further determined the effect of photooxidation aging on the tensile and interfacial adhesion behavior of EA with different cross‐linking network structures through molecular simulation. Based on the molecular models of EA and the interface model between EA and aggregate, the crosslinking network structural characteristics and tensile mechanical behavior were determined. The interfacial adhesion behavior and the mechanization were further studied. The results indicate that 20‐EA and 6‐EA have an epoxy resin cross‐linked network with uniform pore structure and phase distribution. 2‐EA showed a denser cross‐linking network and uneven aggregation phenomenon. Photooxidative aging alleviated the aggregation phenomenon. A dense cross‐linking network improved the tensile strength and the ability of tensile performance to resist photooxidation aging. The interface of EA‐quartz exhibited higher adhesion strength than EA‐calcite due to the closer distance and stronger nonbonding interactions between EA and quartz. The low anhydride content and photooxidation aging made EA approach to the aggregate interface, increasing nonbonding interaction and interfacial adhesion strength. In addition, quartz aggregates were more suitable for application in EA mixtures due to the higher interfacial adhesion strength and lower water sensitivity. [ABSTRACT FROM AUTHOR]

Although styrene acrylate emulsions (SAE) have demonstrated promising applications as surface sizing agents for paper, their strengthening effect on pulp fibers in papermaking is not clear. In this study, bagasse fibers, an agricultural waste, were treated with SAE to study the influences on the mechanical properties of the produced papers. SAE copolymers with hard chain (H‐PSA) and soft chain (S‐PSA) were prepared and added to bagasse pulp slurry at concentrations of 1%–4% by weight. The findings indicated that for the soft and hard copolymers, the glass transition temperatures were 19.5 and 26.8°C and their emulsion particle sizes were 166 and 182 nm, respectively. The copolymers strengthened the produced paper by wrapping around and forming a network of chemical and physical bonds with the pulp fibers. Papers treated with 3% H‐PSA exhibited the optimum improvement in tensile strength (38 MPa) and breaking length (67 m) by 13% and 64%, respectively. Treated papers were negatively affected by UV radiation due to phenyl groups spread along the chains. The copolymers demonstrated good wet‐strength properties achieved by self‐ and co‐crosslinked networks. The prepared paper sheets showed a preference for the mechanical properties of treated samples over the untreated ones. [ABSTRACT FROM AUTHOR]

Asphaltenes and waxes are the primary factors affecting the cold flow properties of crude oil. In this paper, based on the binary polymer of acrylate‐maleic anhydride (PM22‐MA), different third polar groups of acrylamide, N‐(hydroxymethyl) acrylamide, N‐phenylacrylamide (NPA), and styrene (SM) were introduced to synthesize a series of ternary pour point depressants (PPDs) to explore the effect of asphaltene on the cold flow properties of Xijiang (XJ) crude oil. Thereinto, PM22‐MA‐NPA containing amide group and benzene ring exhibited the best depressive effect, which decreased pour point by 14°C at 1500 ppm. The mechanism of interaction of the polar groups in PPDs with asphaltene was studied. The polar groups could form stronger hydrogen bonds with asphaltene, delaying the asphaltene macromolecule bonding, allowing the synergistic effect of PPDs and asphaltene to be better utilized to improve the cold flow properties of crude oil. Furthermore, the dipole moment magnitude and electron cloud density were calculated with Gaussian. It was found that the polar group with a dipole moment magnitude of 3.2244 debye and an electron cloud density ranging from −1.6364 to 1.9944 eV was the most suitable third polar monomer for the PPDs of XJ crude oil. [ABSTRACT FROM AUTHOR]

Poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) (PHBV) is a biodegradable polymer with significant potential for use in food packaging. However, its limited melt strength poses a challenge when employing film‐blowing techniques to produce flexible packaging. To overcome this obstacle, we developed blends consisting of 70 wt% PHBV and 30 wt% poly(butylene‐co‐succinate‐co‐adipate) (PBSA). Organic peroxides such as dicumyl peroxide and 2,5‐dimethyl‐2,5‐di‐(tert‐butylperoxy)hexane, were utilized as reactive compatibilizers to enhance the interfacial adhesion between the polymers. Additionally, acetyl tributyl citrate (ATBC) was employed as a plasticizer to improve processability and ductility. The inclusion of organic peroxides resulted in the formation of long‐branched structures, as confirmed by the van‐Gurp‐Palmen plot. The melt flow index decreased from 30 to 9.8 g/10 min without ATBC and 15.5 g/10 min with ATBC. Successful production of blown PHBV/PBSA films was achieved on a pilot scale (bubble height 180 cm). These films exhibited heat‐sealing capability and increased impact strength (7.7 kJ/m2). Moreover, the films maintained a maximum elongation at break of 4% during a 3‐month storage experiment with frozen food. Food safety was assessed through overall migration experiments, and the non‐plasticized films received approval. In conclusion, the compatibilized PHBV/PBSA blends demonstrate great potential as materials for manufacturing film‐blown flexible packaging. [ABSTRACT FROM AUTHOR]

The disposal of plastic foam, mostly composed of polystyrene, poses significant environmental challenges due to its high popularity, slow degradation, and low cost. To address this problem, recycling polystyrene foam waste (PF) has emerged as a promising solution to reduce plastic pollution. This paper presents a novel approach to mass‐produce highly ordered, porous honeycomb‐patterned film (hc‐film) using wasted PF as the raw material. The hc‐film is produced using an improved phase separation (IPS) method that utilizes methanol as a suitable pore inducer and template droplet stabilizer. Methanol provides the hc‐film with customizable features such as pore ordering, size, and separation. The freestanding hc‐film, achieved by adopting a water‐soluble polystyrene sulfonate as a scarified layer, can be transferred and utilized as a flexible mold to pattern various solid substrates with complicated surface morphologies using the pre‐impregnated technique. This study demonstrates the potential of this cost‐effective and efficient approach for various applications, such as super/anti‐wetting surfaces, microelectronics, optical devices, sensors, and nanogenerators. [ABSTRACT FROM AUTHOR]

In this paper, the influence of different material trademarks, mass ratios, the melt mass‐flow rate (MMFR) and molecular weights (MW), mold and injection temperatures, Al2O3 powder and lignin on the shape memory properties of PLA/PCL SMP material (PPSM) were then analyzed in detail by different characteristic methods. Besides, three promising applications (Origami metamaterials and variable‐stiffness grippers) are provided utilizing the PPSM doped with Al2O3/lignin. Eventually, a compensating strategy was discussed to improve the final configuration of the SMP after multi‐cycles. The shape memory recovery ratios could be improved by increasing the MMFR of PLA and the MW of PCL. The addition of 2 g‐Al2O3 could shorten the recovery time, while the addition of 2 g‐lignin could increase the thermal‐recovery force and mechanical performance. The shape memory rate under 20 g weights, initial peak forces at room and high temperatures of the origami metamaterials could reach 57%, 2027.29 N and 17.49 N, respectively. The tensile force of banding rebars could reach 150.29 N, which is promising to apply into the construction field. [ABSTRACT FROM AUTHOR]

Regenerated cellulose membrane is a biomaterial obtained by activating, dissolving, solidifying, and regenerating cellulose powder using solvents of different polarities. It has the characteristics of high oxygen resistance and high strength. However, its low water vapor barrier and single function limit its application. In order to improve the water resistance of regenerated cellulose membranes and endow them with UV resistance, lignin was extracted from waste wheat straw using formic acid method. The extracted formic acid lignin (FAL) was added to the cellulose solution to prepare a series of regenerated lignocellulosic membranes (RC‐FAL) with different lignin contents. The results indicate that lignin can not only improve the water vapor barrier, tensile strength, and water resistance of the film, but also enhance the oxygen barrier and UV absorption of the film. Compared with pure cellulose film, the contact angle of lignocellulose film can be increased by 66.2%, the UV absorption rate can reach 100%, and the oxygen transmission coefficient has no significant effect. In this paper, a new kind of biological packaging material with high oxygen resistance, strong ultraviolet absorption, and water resistance was prepared by recycling waste wheat straw, it has a broad application prospect in the industrial production of packaging materials. [ABSTRACT FROM AUTHOR]

The article titled "Correction to 'A new slit-radial die for simultaneously measuring steady state shear viscosity and first normal stress difference of viscoelastic liquids via capillary rheometry'" published in the Journal of Applied Polymer Science contains a correction to Equations 17-19 and 22. The correction replaces the minus sign with the plus sign in these equations. The corrected equations are provided in the article. The results presented in the paper are not affected by this typo. The authors apologize for the error. [Extracted from the article]

Electrospinning is an economical, efficient, and versatile process for the preparation of continuous nanofibers with desired patterns, tailored fiber diameters, and orientations. Since its invention, electrospinning has been utilized to prepare nanofibers from several natural polymers and synthetic polymers for use as scaffolds in tissue engineering, regeneration, and biomedical applications. Furthermore, complex scaffolds were prepared by electrospinning complex polymer solutions formulated by blending natural and synthetic organic polymers with bioceramics and other inorganic molecules. Lately, coaxial electrospinning has emerged as a promising technology in the preparation of drug‐loaded biodegradable core‐shell structured micro/nanofibers for sustained drug delivery applications. This paper will discuss the basic mechanism of electrospinning, parameters governing the electrospinning process, various materials investigated for use in the electrospinning process, and its recent advances. [ABSTRACT FROM AUTHOR]

This paper presents an extensive experimental investigation on fatigue properties of carbon‐black filled isoprene rubber under complex loadings. A basic life prediction model taking strain energy density as fatigue parameter is first proposed based on fatigue crack growth tests and uniaxial tension fatigue tests under relaxing loads at room temperature. A database of fatigue life including relaxing and non‐relaxing is established through a great number of fatigue tests under five temperatures. Based on the database, two empirical parameters, that is, temperature factor (NRT/NHT) and life reinforcement factor (Re), are introduced to quantitatively characterize the coupling effects of high temperature and non‐relaxing loads on fatigue life. The fatigue mechanisms under different conditions are compared via wide‐angle x‐ray diffraction tests and postmortem analysis. It reveals that the weakening of life reinforcement at high temperatures is closely related to the strain induced crystallization behavior of rubber. [ABSTRACT FROM AUTHOR]

In this paper, we present the synthesis of poly(β‐amino ester)‐based solid polymer electrolytes (SPE) from off‐stoichiometric acrylate‐amine formulations using one‐step, catalyst and solvent free aza‐Michael addition. By varying the monomers, the pendant functionality of the polymer chain structure could be altered. All synthesized polymers yield freestanding and easy to handle electrolyte films and hence are evaluated as a new class of SPEs. The SPE with 1,4‐butanediol diacrylate and propylamine showed the highest conductivity of 1.15 × 10−7 S cm−1 at 30°C with 10 wt% lithium bis(trifluoromethanesulfonyl)imide. Because of the presence of the various functional groups in the structure, the polymer chain aids in the movement of both the anion and the cation. [ABSTRACT FROM AUTHOR]

The synthesis of hollow latex particles through seeded emulsion polymerization involves a series of intricate steps, including the formation of distinct polymer layers with specific properties. Despite extensive research, preserving the desired hollow structure remains challenging due to the unclear role of the encapsulating polymer layers. This study systematically adjusts the glass transition temperature (Tg) of the intermediate layer by varying the butyl acrylate (BA) ratio in the monomer feed mixture. By controlling the reaction temperature during alkali swelling, we explore the critical influence of Tg on hollow latex particle formation from carboxylated core latex particles. To ensure long‐term hollow structure retention after drying, a rigid outer layer is polymerized onto the intermediate layer. Surprisingly, higher divinylbenzene (DVB) mass ratios (5.0 and 10.0 wt%) do not result in a highly crosslinked hollow shell due to DVB self‐nucleation. This paper emphasizes the importance of precise design parameters for both intermediate and outermost layers in achieving and maintaining hollow latex particle structures. Understanding each layer's role and optimizing their compositions contribute to advancing hollow latex particle synthesis through seeded emulsion polymerization. [ABSTRACT FROM AUTHOR]

As an environmentally friendly biomacromolecular material, microcrystalline cellulose (MCC) enhances the performance of natural rubber latex (NRL) composites. However, MCC has strong polarity, which weakens the interfacial interaction between MCC and the non‐polar NRL matrix and reduces the reinforcing performance due to the many hydroxyl groups on its surface. In this paper, the ionic liquid (IL) modified MCC/IL material was prepared, and AIR‐FTIR, x‐ray diffraction, and XPS photoelectron spectroscopy were performed to detect it from the perspective of environmental protection. And natural latex/microcrystalline cellulose/ionic liquid (NRL/MCC/IL) composites with excellent properties were prepared by latex blending. The activation energy, vulcanization characteristics, basic mechanical properties, dynamic mechanical properties, and filler‐rubber interfacial interactions of NRL/MCC/IL composites were investigated. The results showed that the vulcanization rate constant of NRL/MCC/IL composites increase, the activation energy decreases and the mechanical properties were significantly improved. At the same time, the matrix interface interaction of composites was quantitatively calculated using Ayala parameters. The results showed that the interfacial interaction force of the composite was stronger after an appropriate amount of IL pretreatment. The whole process is not only conformed to the concept of green development, but also broadens the application of MCC in rubber materials. [ABSTRACT FROM AUTHOR]

Calcium carbonate is one of the most common scaling minerals. In this paper we have used different electrical current modes (direct current [DC], pulsed DC, and alternating current [AC]) to control the amount, morphology, and distribution of calcium carbonate deposit on electroconductive epoxy/carbon nanofiber (CNF) coating. The effect of different current modes on surface scaling was visualized using scanning electron microscopy. It has been shown that both AC and DC anodic polarization limited scale deposition on epoxy/CNF coated surfaces, although the mechanisms of scale inhibition during AC and DC polarization were different. DC polarization of the coating at +2 V resulted in the smallest scale buildup without leading to coating degradation, while DC polarization at potentials as high as +5 V caused the coating to degrade. Interestingly, application of pulsed DC with high pulse frequency (50 Hz) inhibited the degradation. The type of current applied affected also the morphology of the precipitate at the cathode. The results presented in this work show, for the first time, how different modes of electrical current applied to electroconductive composite coatings can be used to control the morphology and distribution of calcium carbonate scale, and how the organic coating degradation at high polarization potentials can be avoided. [ABSTRACT FROM AUTHOR]

Paper‐based materials are widely used in various fields due to their advantages, such as environmental friendliness and sustainability. However, the highly hydrophilic nature of the cellulose that makes up paper‐based materials limits their use. In this paper, micron/nano‐graphite/polydimethylsiloxane (PDMS) coatings with excellent superhydrophobic and conductive properties were prepared on the surface of filter paper by a simple spraying method. A mixture of micro‐graphite and nano‐graphite was used to form a multistage rough structure on the surface of the filter paper by spraying, and the low surface energy PDMS enhanced the adhesion of the micro‐graphite and nano‐graphite on the surface of the filter paper. The results showed that the samples possessed the best superhydrophobic properties when the ratio of micro‐graphite to nano‐graphite was 1:1, at which time the contact and rolling angles of the samples were 165.4° and 3.2°, respectively. The prepared superhydrophobic samples have good bounce and self‐cleaning properties, while the samples have good mechanical stability and chemical resistance. Additionally, due to the conductivity of micro–nano‐graphite, both particle sizes closely contact the sample surface, creating a conductive network. With a 1:1 ratio of micro‐ and nano‐graphite, the coating exhibits minimal resistance at 1.89 KΩ, and the sample maintains stable conductivity even underwater. The above properties greatly extend the application range of paper‐based superhydrophobic materials. [ABSTRACT FROM AUTHOR]

Humans generate a lot of irregular movements in their daily lives, and much of the movement energy is difficult to collect. This paper develops a wearable device based on a liquid metal (LM)‐based frictional electric nanogenerator, including: flexible power‐generating fiber, power‐generating surface, and power‐generating insole. Friction nano power generation fibers are prepared using LM, epoxy resin, and silicone. The power generation device could be formed by weaving the fibers in cross, mesh and spiral arrangement, with a maximum open circuit voltage of 142 mV and current of 1.06 A, which could be coded into intelligent clothing. Power generating surfaces use LM, nylon,polycaprolactone (PCL), and polyethylene terephthalate (PET) as friction electrodes. The LM‐PCL produces a maximum open‐circuit voltage of 2.4 V and a maximum current of 1.23 A when they form a friction electrode. Electricity‐generating insoles are composed of silicone holes filled with LM, and the movement of the human foot generates electricity. With a friction area of 18.75 cm2, a maximum output voltage of 221 mV is obtained. These friction nano power devices have the advantages of a green environment, and low cost, which could be widely used in medical, biological, and clothing formulation fields. [ABSTRACT FROM AUTHOR]

In this paper, uniformly transition metal oxide (MoO3) nanosheets were electrochemically deposited on flexible carbon cloth (CC), and then conductive polyaniline (PANI) was orderly wrapped around their surface by electrochemical polymerization. The morphology and structure of as‐obtained self‐supported PANI/MoO3/CC electrode were investigated by FTIR, X‐ray diffraction, Raman, scanning electron microscope (SEM), transmission electron microscopy (TEM), and X‐ray photoelectron spectroscopy measurements in detail. Among all PANI/MoO3/CC electrode, the self‐supported PMC‐3 (deposition time of 300 s) has high specific capacitance of 841.6 F g−1 at current density of 0.5 A g−1 in the three‐electrode system, having specific capacitance of 595.7 F g−1 even at 10 A g−1. Novelty, the as‐assembled symmetrical capacitor is flexible and convenient with power density of 199.93 W kg−1 at the energy density of 9.69 Wh kg−1 and the energy density of 3.88 Wh kg−1 at power density of 4000 W kg−1. Thus, the electrochemical properties of the self‐supported PANI/MoO3/CC electrode were significantly improved, and the self‐supported electrodes are more competitive than other materials in practical application of clean energy storage systems. [ABSTRACT FROM AUTHOR]

In this study, paper coated with a polyamide film containing a molecularly imprinted polymer (MIP) of benzalkonium chloride (BKC) is prepared. Its BKC adsorption ability and selectivity for BKC adsorption are investigated. The MIP is prepared by agitating an ethylenediamine solution containing an azo initiator, BKC as a template material, and methacrylic acid (MAA) as the functional monomer. First, filter paper soaked in this mixture is impregnated with a cyclohexane solution of terephthaloyl chloride and a BKC–MAA–MIP‐containing polyamide film is prepared on the surface of the paper. Paper containing BKC–MAA–MIP adsorbs BKC. The paper with the highest BKC removal efficiency is prepared under the following conditions: 4 mL MAA functional monomer, 2.5 w/v% ethylenediamine, and 10 min MIP synthesis time. The paper with BKC–MAA–MIP selectively adsorbs BKC from a solution containing BKC, tetracycline hydrochloride, and caffeine. Thus, a polyamide film containing BKC‐MAA‐MIP formed on paper can effectively and selectively remove BKC from aqueous environments. [ABSTRACT FROM AUTHOR]

In this paper, the thermal stability and degradation mechanisms of C60 fullerene‐based polymers, obtained by click polymerization between dialkyne‐substituted C60 derivative monomers and 1,3,5‐tris(dodecyloxy)benzene‐based diazide comonomers, were evaluated. The activation energy of the fullerene polymer C60P2 with an ethylene spacer, determined under peak degradation rate conditions, was lower than that of the counter polymer C60P1 with a methylene spacer, suggesting lower thermal stability of C60P2. The combined technique of thermogravimetric analysis—mass spectroscopy and Fourier transform infrared spectroscopy revealed that the thermal decomposition onset of the analyzed samples is accompanied by CC cleavage of the dodecyloxyside chain groups, followed by the decomposition of the 1,2,3‐triazole, dicarboxylate and benzoate moieties. It was found that no thermal decomposition of the fullerene carbon cage occurs up to 670°C. Molecular modeling with Hyperchem software version 7.5 confirmed that C60P1 is more thermally stable than C60P2. [ABSTRACT FROM AUTHOR]

In this paper, three epoxy resin systems commonly used in power equipment are prepared to obtain cross‐linked networks with structural differences. The relationship between microscopic structures and dielectric properties of epoxy resins is investigated and discussed. Experimental results show that the polarization and conductance losses are inhibited in the anhydride‐cured systems with methyl groups. The molecular dynamics (MD) simulation shows that rigid anhydride structures (such as methyl groups) play a major role in reducing the local segment mobility and increasing the free volume at cross‐linking points. The decrease in local segment mobility has been confirmed by the decrease of mean square displacement (MSD) at the cross‐linking points, which is consistent with the change of measured polarization and conductance loss. In the glassy state, the dielectric properties of different anhydride‐cured systems can be reflected by local MSD at the cross‐linking points. At high temperatures near the glass transition temperature, both the free volume and network mobility increase significantly, which reflects the increased dielectric relaxation strength and conductance loss. The understanding of the structure–property relationships could provide a theoretical foundation for epoxy modification in a controlled manner for power equipment applications. [ABSTRACT FROM AUTHOR]

Super‐hydrophobic surface is widely used in waterproof, antifouling, and anticorrosion fields because of its unique wetting characteristics. However, the rough structure of super‐hydrophobic surface is easily damaged in service, which leads to the loss of various properties, making it difficult to apply super‐hydrophobic surface on a large scale in actual production. In this paper, epoxy resin was used as adhesive, mixed with hydrophobic silica particles and sprayed on the surface of carbon fiber composites. After curing, the surface of super‐hydrophobic carbon fiber composites with contact angle of 158 ± 2° and sliding angle of 1 ± 0.5° was formed. The surface had excellent dynamic water repellent performance, and the droplets could bounce more than three times on the surface. Furthermore, the super‐hydrophobic surface had excellent wear resistance and mechanical stability. After the friction damage test, the surface structure of the sample was slightly damaged. The amount of wear was small, and the surface was still in super‐hydrophobic state. Through soaked in solutions with different pH values, the microstructure of the surface was not obviously damaged by corrosion, the contact angle of water droplets was greater than 155°. The preparation method of super‐hydrophobic surface of carbon fiber composite proposed in this study is simple and rapid, and the prepared surface has excellent performance, the practical application of super‐hydrophobic surface is promoted. [ABSTRACT FROM AUTHOR]

A tremendous amount of the nonbiodegradable microplastic waste has been generated after the outbreak of COVID‐19 by the widespread use of single‐use personal protective equipment, especially disposable medical masks (DMMs). This has caused harm to the health and safety of human beings and various organisms. Finding a way to properly deal with these single‐use medical wastes has become an urgent problem. In this paper, an innovative way was explored to use DMMs in geopolymer (GP). The physical properties, mechanical strength, and resistance to high temperatures (200–800°C) of the composites were investigated. The findings of the study revealed that DMMs had negligible influence on resistance to high temperatures, but showed a positive influence on enhancing the compressive and flexural strengths of GPs at ambient temperature. The optimum DMMs content was 0.4 wt%, at which the compressive and flexural strengths of the GP composites were enhanced by 5.8% and 22.68% compared with the pure GP, respectively. The same polypropylene (PP) fiber amount increased compressive and flexural strengths by 7.49% and 9.76%, respectively. This thus confirmed that DMMs can be sustainably utilized in green building materials, playing a role as PP fibers toughening and contributing to the effective management of waste plastics. [ABSTRACT FROM AUTHOR]

This study investigates the effect of 1,2,3,4‐butane tetracarboxylic acid (BTCA) crosslinking treatment on the electrical properties of poly‐p‐phenylene terephthalate (PPTA)/cellulose insulation paper to prepare a novel composite insulation paper with low dielectric constant and good electrical performance. Three‐layer PPTA/cellulose composite paper crosslinked by BTCA under various conditions, composite paper without crosslinking, directly mixed composite paper, and conventional Kraft paper are prepared. The morphology and surface chemical composition of the paper samples are characterized. Dielectric, mechanical, and thermal properties are investigated. Results show that the BTCA concentration of 0.2 mol L−1 with a 180°C curing temperature is the relatively superior crosslinking condition to prepare a novel composite with low dielectric constant and good comprehensive performance. The dielectric constant and loss of the novel composite paper decrease to 3.21 and 0.392 at 50 Hz. The tensile strength of the BTCA crosslinked three‐layer PPTA/cellulose composite paper (thickness: 130 μm) has reached 10.01 kN m−1, increased by 41.6% than the directly mixed composite paper. The novel BTCA crosslinked composite paper also shows improved thermal stability. The BTCA crosslinking proves to be a promising method to improve the dielectric properties and electrical performance of the PPTA/cellulose composite paper. [ABSTRACT FROM AUTHOR]

This paper reported the novel supercritical carbon dioxide (scCO2) secondary foaming and molding strategy to prepare the thermal‐insulation polyethylene terephthalate (PET) bead foam part with good interfacial adhesion and high expansion ratio. The incorporation of porous structure could effectively enhance the blowing agent solubility and fabricate the system viscosity difference, which contributed to the expansion and further welding of the expanded PET beads. Under the optimum foaming conditions, PET bead foam parts with excellent comprehensive performance were successfully prepared by molding method in the confined space via scCO2 secondary foaming, and the corresponding welding mechanism of PET beads was further investigated. The obtained foam parts possessed good tensile and compressive properties, reaching 1.03 and 1.27 MPa (at 20% strain) respectively. Besides, the foam part exhibited the low thermal conductivity of 0.060 Wm−1 K−1, which confirmed the improvement of thermal insulation performance owing to the high expansion ratio. [ABSTRACT FROM AUTHOR]

This paper presents detailed curing kinetics models for two thermoset adhesives. The cure kinetics were characterized using differential scanning calorimetry in both anisothermal and isothermal modes. The Sestak–Berggren autocatalytic model was applied to describe the anisothermal cure kinetics of the two adhesives with the Malek and undetermined coefficients methods determining their kinetic parameters. The Kamal autocatalytic model was adopted for the isothermal curing processes with the Kenny analytical‐graphical method determining the kinetic parameters. A modified Kamal model was developed by introducing a concept of the maximum degree of cure (DOC) and temperature‐depended kinetic parameters to describe the isothermal cure kinetics of the adhesive with a typical exothermic peak, and an extended Kamal model was further proposed by adding an initial‐phase‐control term to the modified Kamal model to describe the isothermal cure kinetics of the adhesive with two exothermic peaks. The results showed that the presented curing kinetics models with the determined parameters can precisely predict the evolutions of the DOC of the two thermoset adhesives in both anisothermal and isothermal modes. [ABSTRACT FROM AUTHOR]

In this study, soapstone waste originated from craftsmanship activities was used as an alternative filler (0–30 wt%) for a high‐density polyethylene (PE) matrix. The aim of this paper is to understand the effect of the filler particles on crystallinity, thermal stability and thermo‐mechanical properties of this newly developed composite material. Physico‐chemical characterization was performed by x‐ray diffraction (XRD) and Fourier‐transform infrared (FTIR) spectroscopy. Thermogravimetric analysis (TGA), oxidation induction time (OIT) and dynamic mechanical thermal analysis (DMA) were performed to assess the effect of the filler on the themo‐mechanical properties of PE. Thermal stability, measured by TGA, was enhanced, while OIT values reduced with filler content. A significant increase on the storage modulus of the composites (up to 148% in comparison with unfilled PE) was observed and this reinforcing effect was even more prominent at higher temperatures. XRD analysis revealed that the degree of crystallinity improved significantly with soapstone loading, which explains the substantial increase in stiffness observed. Increased crystallinity is also associated with higher strength, reduced residual stress, and better dimensional stability of end products, which can be particularly attractive for pressure pipe applications. [ABSTRACT FROM AUTHOR]

Polypropylene (PP) becomes a superior candidate material for new environmentally friendly cable main insulation with its excellent heat resistance, electrical properties, and degradability. However, in practical application, PP material is aging and vulnerable and its toughness is poor. The mechanical properties of PP material can be improved by elastomer modification, but the effects of different elastomers on the comprehensive properties of composite specimens are quite different. In this paper, the electrical and mechanical properties of different types of elastomer‐modified PP composites are compared and analyzed by combining experimental and molecular simulation (MS) methods. The experimental results show that the SEBS/PP composite material has the lowest trap energy levels among all kinds of composite materials, its space charge accumulation is 1.96 × 10−9C, and the mechanical and rheological properties improvement of the composite is the most remarkable. Meanwhile, the volume resistivity is reduced by two orders of magnitude compared with pure PP. However, the breakdown strength of all kinds of composite materials decreases by different degrees after the modification. The solubility parameters (δ) and the free volume are further investigated by the molecular simulation, which shows that the δ of SEBS is similar to that of PP, which represents the best compatibility. Moreover, the SEBS/PP composite material has the strongest inter‐molecular force and the most excellent toughness improvement for PP. This work provides a theoretical basis for elastomer selection in PP modification. [ABSTRACT FROM AUTHOR]

Conventional adhesives often emit volatile organic compounds (VOCs), which have a negative impact on human health. In this paper, an environmentally‐friendly supramolecular adhesive PD which has high adhesive and low VOCs emission is prepared by the reaction between polyethyleneimine (PEI) and 3,4‐dihydroxybenzaldehyde (DBA). PD containing abundant catechol groups exhibit excellent adhesion to wood substrates and is able to reach a maximum shear strength of 5.20 ± 0.39 MPa. One factor is attributed to multiple reactions between PEI, and DBA and oxidation of DBA. These reactions construct a complex three‐dimensional cross‐linked structure which is very helpful to improve the bonding performance of the adhesive. Another reason refers to the fact that a large number of catechol groups in PD can form a lot of hydrogen bonds with the amino group in PEI and the hydroxyl group in the wood substrate. These hydrogen bonds play an important role in enhancing shear strength. PD adhesives have a stronger bond strength than commercial chloroprene rubber (CR, Pattex‐PXL) and polyvinyl acetate adhesives (PVAc, JUJU‐8708) and have lower emissions of VOCs. As an environmentally‐friendly adhesive for wood‐based substrates, this adhesive may have potential applications in the wood processing industry. [ABSTRACT FROM AUTHOR]

In this paper, activation oil added with temporary blocked isocyanate was chosen to enhance interfacial adhesion in polyethylene terephthalate (PET) high‐strength fibers reinforced rubber via one‐step dipping method, in which the temporary blocked isocyanate could be activated during vulcanization process of rubber. The effect of isocyanate in enhancing adhesion between PET high‐strength fibers and rubber was explored. The amount of residual resorcinol formaldehyde latex on the surface of fibers and H‐extraction force of PET high‐strength fibers reinforced rubber are both obviously increased with 5% activation oil addition especially containing 2% isocyanate. After peeling fibers from composite rubber, the amount of residual rubber on the surface of fibers with activation oil is increased, which is even higher when further adding temporary blocked isocyanate. Based on the results of infrared spectra and nuclear magnetic resonance carbon spectra, the added isocyanate is confirmed to bond with the PET component most likely through reacting with the terminal hydroxyl groups on the surface of PET fibers. This interface reinforcement strategy based on one‐step dipping method will contribute to studies on PET high‐strength fibers reinforced rubber. [ABSTRACT FROM AUTHOR]

Today a wide variety of wearable electronics are in our daily lives and their uses are increasing. The development of portable, flexible, lightweight, cost‐effective, and stable devices that produce sustainable energy with renewable approaches in the field of wearable electronics, as in every field, is one of the important issues of today. According to their volume and weight, the use of nanofibers with high surface area in energy‐generating devices may bring them advantages such as lightness and higher energy density. Therefore, in recent years, researchers have focused on the development of nanofiber‐based nanogenerators that produce energy using mechanical energy in a sustainable and renewable way. In this paper, self‐standing piezoelectric nanogenerator (PENG) fabrics were obtained by developing flexible composite poly(vinylidene fluoride) (PVDF) nanofiber yarns doped with zinc oxide (ZnO) nanoparticles at different rates to provide higher power output. It has been characterized from electromechanical, structural, and morphological aspects. The most successful self‐standing PENG fabric obtained (at 5% ZnO loading) doubled the energy output of the fabric made from pure PVDF nanofiber yarn and provided a peak total power of 81 μW and a power density of 30 μW/cm2. The present results open up the field for the development of PVDF/ZnO‐based nanomats and their use in sensors and actuators in the healthcare and engineering industries. [ABSTRACT FROM AUTHOR]

As an eco‐friendly technology for pavement preventive maintenance, microsurfacing (MS) has the potential properties of cost‐saving and excellent performance benefits in repairing distress. MS also improves the surface function, especially skid resistance, of old pavements that have gradually decayed under the coupled effects of long‐term environment and loads. Reasonable assessments of the long‐term skid and wear resistance of the MS can provide support for accurate decision‐making on preventive maintenance, which in turn reduces maintenance costs and saves maintenance costs, and ensures traffic safety. To evaluate the long‐term skid and wear resistance of MS in different natural and traffic environments, this paper investigated the change of British pendulum number (BPN), rutting depth, and mass loss rate of waterborne epoxy resin‐SBR compound emulsified asphalt micro‐surfacing (WER‐SBR MEAMS) under different environmental factors and traffic conditions based on the self‐developed accelerated loading abrasion instrument. The factors considered in the experiment include temperature, rainfall, UV radiation, speed, and load. The results showed that temperature and vehicle speed had a detrimental effect on the durability of WER‐SBR MEAMS, which was more pronounced after 10,000 wear loading cycles. Reducing immersion time and slowing down the aging rate can improve the durability of WER‐SBR MEAMS. Further, the influence degrees of different factors on the skid and wear resistance of MS were evaluated using the gray correlation method. From the results of the gray correlation analysis, the correlation coefficients between external variables and BPN, rutting depth, and mass loss rate are all greater than 0.8, which indicate that all the variables involved have relatively obvious and regular effects on the skid and wear resistance of WER‐SBR MEAMS. [ABSTRACT FROM AUTHOR]

To investigate the microstructure and mechanical properties of self‐crimping two‐component side‐by‐side bicomponent filament, this paper focuses on systematically investigating the structure–property evolution of poly(ethylene terephthalate) (PET)/poly(trimethylene terephthalate) (PTT) side‐by‐side bicomponent filament prepared via melt spinning with various component ratios, drawing and heating treatment. The investigation was operated upon the combination of morphology analysis, thermal analysis, crystallization, and orientation analysis. The variation of cross section and curl‐morphology, crystallization, and microstructures mainly containing lamellar and microfibrillar crystals as well as their effects on the mechanical and self‐crimping properties were discussed. As the draft ratio (DR) increases, the crystallinity, sonic orientation factor, tensile strength, and crimp‐recovery rate of the filaments were increased. The sonic orientation factor in the crystalline region decreases from 0.923 to 0.777 but increases from 0.677 to 0.903 in the amorphous region. In contrast to the variation of the DR, heating temperature has a limited effect on the tensile strength of the PET/PTT hybrid filaments. Crimp‐recovery rate, however, first increases to 11.8 and then decreases to 9.8 with an increasing heating temperature from 144 to 168°C. Most of these behaviors have been attributed to changes in the ratio of contractile stress for both PTT and PET components, originating from microstructural evolution in hybrid filaments, including crystal growth, breakage, deflection, and deformation of chains along the axial direction. As a summary, an interpretive diagrammatic sketch has been proposed to clarify the structure–property relationships of the commercial PET/PTT filaments. [ABSTRACT FROM AUTHOR]

In order to improve the flame‐retardant performance of insulating paper and reduce the fire risk, hydroxyethyl diphosphate and dicyandiamide were used to modify starch to prepare a new starch‐based flame retardant (SHPD). The combustion, mechanical, and electrical properties of SHPD treated flame‐retardant insulating paper were investigated. The results showed that when the impregnation concentration of SHPD was 25.0%, the limiting oxygen index of the insulating paper was increased from 18.3% to 38.3% and reached the level of UL‐94 V‐0. The tensile index and burst index of the flame‐retardant insulating papers were only 10.17% and 12.5% lower than that of the control insulating paper. The ring crush strength and alternating current breakdown strength in air of the flame‐retardant insulating papers were 63.3% and 1.8% higher than that of the control insulating paper. The SHPD flame retardant has a good application prospect in insulating paper. [ABSTRACT FROM AUTHOR]

Chloroprene rubber (CR) is frequently quoted as an example of strain‐induced crystallizing elastomer. Many researchers have focused on studying the aging mechanism and mechanical properties of aged CR, little has been done on the effect of crosslinking structure on strain‐induced crystallization (SIC). The present paper related systematic investigations combining the changes of crosslinking structure and its influence on SIC. It was firstly investigated based on FTIR, crosslinking density test and GPC. The results showed that the molecular chains were oxidized in the early stage of aging, but the crosslinking reaction still dominated. At the same time, sol content and polydispersity decreased. In the later stage of aging, CR was oxidized, resulted in severe molecular chains fracture and an increase in the free sol content and polydispersity. The impact of aging on SIC under tensile condition was further investigated by the tensile tests. An obvious stress‐hardening was found for unaged CR, but not in aged CR. The crystallinity and microcrystalline region orientation tests showed that oxidation, crosslinking by double bonds and dechlorination during aging were not conducive to the orientation of molecular chains during stretching. It is the aging process that has an adverse effect on the SIC of CR. [ABSTRACT FROM AUTHOR]

The design of environment‐friendly fireproof rigid polyurethane foams (RPUFs) that completely prevent ignition or the spread of fires is important for energy conservation and emission reductions. In this paper, an intumescent flame‐retardant coating was prepared and coated onto the surface of a RPUF to improve its flame retardancy. Vertical combustion experiments (UL‐94) showed that, compared with the pure RPUF, a RPUF coated with the expansion coating successfully self‐extinguished without a droplet formed after ignitor removal. Thermogravimetric analyses showed that the expanded coating effectively increased the rate of carbon residue formation. Cone calorimetry showed that when the pigment‐to‐binder ratio was 3.5:1, with 5% modified montmorillonite, 6% aluminum hydroxide, and 4% titanium dioxide, the intumescent coating effectively reduced the heat release rate and total heat release of the RPUF. Remarkably, the smoke release rate and total exhaust gas volume showed that the expanded coating provided obviously enhanced smoke suppression. Therefore, the flame retardancy and toxic smoke suppression provided by the RPUF thermal insulation material is essential and very useful for healthy development of human society and the environment. [ABSTRACT FROM AUTHOR]

In this paper, a graphene‐oxide/carboxymethyl‐chitosan/polyvinyl‐alcohol (GO/CMC/PVA) composite nanofiber membrane was prepared by electrospinning and cross‐linking with glutaraldehyde (GA) to improve the water resistance. The composite nanofiber membrane can be used in the field of heavy metal adsorption. The membrane was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, and X‐ray diffraction. The effects of GO concentration, adsorption time, and initial concentration of heavy‐metal ion (Ni2+, Cu2+, Ag+, and Pb2+) solution on the adsorption performance of the fiber membranes were investigated. The results showed that the addition of GO can reduce the diameter of nanofibers. GO, CMC, and PVA exhibited good compatibility, and the intermolecular hydrogen bonding improved. The addition of GO also improved the crystalline properties of the composite fiber membrane. In the optimal cross‐linking condition, GA was saturated by steam cross‐linking for 6 h. The introduction of GO improved the adsorption capacity of the membrane for heavy metals in water. The utmost adsorption capacities for Ni2+, Cu2+, Ag+, and Pb2+ were 262.1, 237.9, 319.3, and 413.6 mg/g when using the cross‐linked composite fiber membranes, respectively. The results of adsorption kinetics and thermodynamics showed that the adsorption process accorded with the pseudo‐second‐order kinetic model and Langmuir–Freundlich isotherm model. [ABSTRACT FROM AUTHOR]