Jun Qian

Acrylate hot-melt adhesives (AHMAs) are widely used in medical dressings, electronic components, and automotive interiors due to their solvent-free nature and high bonding strength. However, their wetting behavior on porous fabric substrates under varying coating temperatures—a critical factor for interfacial adhesion—remains poorly understood. To investigate how coating temperature affects the wetting and adhesion of acrylic hot-melt adhesives on fabric substrates, the apparent surface tension and viscosity of the adhesive (130–160 °C) and the apparent surface energy of the substrate (20–160 °C) were measured. By combining these measurements with contact angle decay curves on steel plates, scanning electron microscopy of cold-brittle cross-sections, and mechanical property tests, the study analysed the effects of temperature on wetting and spreading, penetration depth, and adhesive performance. Results show that with increasing temperature, adhesive surface tension and viscosity decrease, while fluidity improves; substrate surface energy shows no temperature dependence. The penetration depth into the fabric increases from 16 μm to 25 μm, and penetration uniformity gradually improves. However, both peel strength and loop tack continuously decrease with rising temperature, with optimal adhesion at 130 °C. A penetration depth model based on the Washburn equation effectively predicts the penetration behavior. Viscosity accounts for more than 50% of the effect, whilst the wetting factor contributes to a lesser extent. This study provides a theoretical basis for optimizing the coating process of acrylic hot-melt adhesives on fabric substrates.

The demand for low‐mid frequency electromagnetic wave absorption (EWA) materials over 5G commercial bands is urgently increasing recently. However, the unpredictable parameter fluctuations in low‐mid frequency EWA performance make it difficult to realize effective microstructure/microcomponent designing. To this end, a feasible strategy is proposed to reasonably optimize the nanoscale dielectric characteristics in high‐entropy materials (HEM). The synergistic grain refinement and lattice distortion enable us to precisely match electromagnetic parameters, therefore enhancing dielectric loss that covers the low‐mid frequency absorption band. In detail, Mn‐doped carbon‐coated high‐entropy alloy nanoparticles (Mn‐HEA@C) allow for enhanced grain refinement, increased grain boundaries and phase interfaces, thereby triggering improved interface polarization and conductive loss. Meanwhile, the increased lattice distortion introduces defect‐induced dipoles that contribute to enhanced relaxation losses. Collectively, Mn ₁ ‐HEA@C realizes efficient coverage of 5G low‐frequency communication bands (N77/78/79) with an effective absorption bandwidth (EAB) of 4.76 GHz, noticeably showing strong absorptions of −50.7 dB at 11.71 GHz and −43.4 dB at 4.91 GHz, respectively. These new findings suggest the nanoscale dielectric gene dual‐regulation strategy greatly contributes to optimized impedance matching and electromagnetic attenuation and lay solid foundations for novel absorbers that emphasize on low‐mid frequency absorption.

Most acrylate adhesives do not bond well to low-surface-energy substrates (e.g., polyethylene and polypropylene) due to the weak interaction force between the polar adhesive molecules and the substrate. To enhance the adhesion performance on low-surface-energy substrates and investigate the effects of substrate surface energy, roughness, pressure-sensitive adhesive (PSA) surface energy, viscosity, and modulus on adhesion performance, this study modifies the acrylate adhesive by incorporating a hydrogenated-terminated hydroxylated polybutadiene (HHTPB) structure with a double bond at one end. The results demonstrate an enhancement in the adhesion performance of the modified PSAs on High-Density Polyethylene (HDPE). The 24 h peel strength and loop tack increase to 4.88 N/25 mm and 8.14 N/25 mm at 20 °C, respectively, with the failure modes remaining adhesive failure. However, as the temperature increases, the peel strength decreases. The high-temperature resistance of the adhesive improves. Based on the experimental data, a mathematical model is proposed that incorporates both the wetting area and loss factor to predict peel strength. The influence of these two factors on the peel strength of the PSA is dependent on the application temperature of the adhesive.

Acrylic pressure sensitive adhesives, modified by polyurethane (PU), achieve selective optimization through the designability of polyurethanes. In this paper, PU macromonomers were prepared by a two-step synthesis method, using polypropylene glycol or polyethylene glycol with different molecular weights as soft segments and different types of diisocyanates: isophorone diisocyanate, hexamethylene diisocyanate, dicyclohexylmethylmethane diisocyanate (HMDI), 2,4-toluene diisocyanate (TDI), and 4,4'-diphenylmethane diisocyanate (MDI) and chain extenders as hard segments. After being terminated by capping agents, a series of PU macromonomers of different molecular weights and structures were obtained and used to modify the acrylic base adhesives. Compared to unmodified adhesives, acrylic adhesives modified by PU macromonomers have improved adhesion performances and heat resistance and show an increasing trend with the increase of molecular weight of diols. Diols with a molecular weight of 600 have the best effect. Diisocyanates containing benzene rings can better improve the thermal performance of adhesives, where P _MDI containing a biphenyl ring is the best, while aliphatic isocyanate groups have a greater improvement in adhesion performance, and the adhesion performance of P _HDI with a long carbon chain is the best.

The development of pulse power systems and electric power transmission systems urgently require the innovation of dielectric materials possessing high-temperature durability, high energy storage density, and efficient charge–discharge performance. This study introduces a core-double-shell-structured iron(II,III) oxide@barium titanate@silicon dioxide/polyetherimide (Fe₃O₄@BaTiO₃@SiO₂/PEI) nanocomposite, where the highly conductive Fe₃O₄ core provides the foundation for the formation of microcapacitor structures within the material. The inclusion of the ferroelectric ceramic BaTiO₃ shell enhances the composite’s polarization and interfacial polarization strength while impeding free charge transfer. The outer insulating SiO₂ shell contributes excellent interface compatibility and charge isolation effects. With a filler content of 9 wt%, the Fe₃O₄@BaTiO₃@SiO₂/PEI nanocomposite achieves a dielectric constant of 10.6, a dielectric loss of 0.017, a high energy density of 5.82 J cm⁻³, and a charge–discharge efficiency (η) of 72%. The innovative aspect of this research is the design of nanoparticles with a core-double-shell structure and their PEI-based nanocomposites, effectively enhancing the dielectric and energy storage performance. This study provides new insights and experimental evidence for the design and development of high-performance dielectric materials, offering significant implications for the fields of electronic devices and energy storage.