熔体温度对气体辅助注射成型PC／PE共混物形态的影响

分别在低温（200℃）和高温（270℃）下制备了聚碳酸酯／聚乙烯（PC／PE）共混物的气体辅助注射成型制品，通过扫描电镜对PC相不同部位的形态观察，发现分散相PC的形变和分布受成型温度的影响比较大。在低温成型时，分散相PC从表层到气道都有变形，而在高温成型时，分散相PC在气道部位几乎没有变形。在形态分析的基础上，探讨了温度对气体辅助注射成型共混物形态的形成和分布的影响机理。     

超临界气体在聚合物加工中的应用

介绍了超临界气体的性质，以及近年来超临界CO2在聚合物加工中的应用，并对此技术住聚合物加工中存在的问题和未来的发展前景进行了总结和展望。     

Preparation and balanced mechanical properties of solid and foamed isotactic polypropylene/SEBS composites

This study presents a self-designed foaming apparatus and routes to manufacture foamed isotactic polypropylene (iPP) blends with uniform and dense cells, using styrene-ethylene-butadiene-styrene (SEBS) block copolymer as toughening additive. The addition of SEBS can clearly enhance the impact strength of solid iPP, iPP blends with a 20 wt% SEBS has obtained high notched impact strength of 75 kJ/m², which is ca. 16 times larger than that of neat iPP. Relatively fine microcellular iPP-SEBS foams with the average cell size of several micrometers, and the cell density of 10⁹ cells/cm³ were fabricated using a batch foaming procedure. Moreover, using our self-designed mold and compression foaming method, iPP-SEBS foams with balanced mechanical properties were produced. With the increasing of SEBS, tensile strength and flexural strength were slightly decreased, but the impact strength was increased clearly. The balanced mechanical properties between stiffness and toughness were achieved after compression foaming.     

Simultaneously improved solid particle erosion resistant and strength of graphene nanoplates/carbon nanotube enhanced thermoplastic polyurethane films

Up to now, it is a major challenge to protect leading edge of the blades from solid particle erosion. Herein, we propose a structure optimization strategy to fabricate non-woven (NW) enhanced thermoplastic polyurethane nanocomposite films (thermoplastic polyurethane [TPU] - NW@G/C_x) with “sandwich - like” structure by hot pressing technology. TPU NW/graphene nanoplates/carbon nanotube (NW@G/C_x) interlayer film were first fabricated by spraying method. Then the interlayer film was laminated between TPU films to fabricate nanocomposite films. Such prepared TPU - NW@G/C_x film shows excellent solid particle erosion resistance and high-tensile strength. For example, the “steel-and-mortar” structure of NW fabric in TPU film results in high-tensile strength of 45 MPa and storage modulus of 21.2 MPa for TPU - NW@G/C_1.0, increasing by 25% and 171% compared with original TPU film (35 MPa, 8 MPa), respectively. In addition, compared with pure TPU film, the “sandwich - like” structure endows TPU - NW@G/C_1.2 with excellent solid particle erosion resistance and the thermal conductivity (0.251 W/m·K). These superior properties extends application of the TPU - NW@G/C_x film on wind turbine blades.     

Hyperelastic,Robust, Fire-Safe Multifunctional MXene Aerogels with Unprecedented Electromagnetic Interference Shielding Efficiency

MXene aerogels have shown great potential for many important functional applications, in particular electromagnetic interference (EMI) shielding. However, it has been a grand challenge to create mechanically hyperelastic, air-stable, and durable MXene aerogels for enabling effective EMI protection at low concentrations due to the difficulties in achieving tailorable porous structures, excellent mechanical elasticity, and desired antioxidation capabilities of MXene in air. Here, a facile strategy for fabricating MXene composite aerogels by co-assembling MXene and cellulose nanofibers during freeze-drying followed by surface encapsulation with fire-retardant thermoplastic polyurethane (TPU) is reported. Because of the maximum utilization of pore structures of MXene, and conductive loss enhanced by multiple internal reflections, as-prepared aerogel with 3.14 wt% of MXene exhibits an exceptionally high EMI shielding effectiveness of 93.5 dB, and an ultra-high MXene utilization efficiency of 2977.71 dB g g⁻¹, tripling the values in previous works. Owing to the presence of multiple hydrogen bonding and the TPU elastomer, the aerogel exhibits a hyperelastic feature with additional strength, excellent stability, superior durability, and high fire safety. This study provides a facile strategy for creating multifunctional aerogels with great potential for applications in EMI protection, wearable devices, thermal management, pressure sensing, and intelligent fire monitoring.     

Grafted MXenes Based Electrolytes for 5V-Class Solid-State Batteries

Polymer blends based solid polymer electrolytes (SPEs), combining the advantages of multiple polymers, are promising for the utilization of 5 V-class cathodes (e.g., LiCoMnO₄ (LCMO)) with enhanced safety. However, severe macro-phase separation with defects and voids in polymer blends restrict the electrochemical stability and ionic migration of SPEs. Herein, inorganic compatibilizer polyacrylonitrile grafted MXene (MXene-g-PAN) is exploited to improve the miscibility of the poly(vinylidene fluoride-co-hexafluoropropylene) (PVHF)/PAN blends and suppress the consolidation of phase particles. The resulting SPE exhibits a high anodic stability with an ionic conductivity of 2.17 × 10⁻⁴ S cm⁻¹, enabling a stable and reversible Li platting/stripping (over 2500 h). The fabricated solid Li‖LCMO cell delivers a 5.1 V discharge voltage with a decent capacity (131 mAh g⁻¹) and cycling performance. Subsequently, the solid all-in-one graphite‖LCMO battery is also constructed to extend the application of MXene based SPEs in flexible batteries. Benefiting from the interface-less design, outstanding mechanical flexibility and stability is achieved in the battery, which can endure various deformations with a low-capacity loss (< ≈10%). This study signifies a significant development on solid flexible lithium ion batteries with enhanced performance, stability, and reliability by investigating the miscibility of polymer blends, benefiting for the design of high-performance SPEs.     

Hierarchical porous onion-shaped LiMn<Subscript>2</Subscript>O<Subscript>4</Subscript> as ultrahigh-rate cathode material for lithium ion batteries

Spinel LiMn₂O₄ is a widely utilized cathode material for Li-ion batteries. However, its applications are limited by its poor energy density and power density. Herein, a novel hierarchical porous onion-like LiMn₂O₄(LMO) was prepared to shorten the Li⁺ diffusion pathway with the presence of uniform pores and nanosized primary particles. The growth mechanism of the porous onion-like LiMn₂O₄ was analyzed to control the morphology and the crystal structure so that it forms a polyhedral crystal structure with reduced Mn dissolution. In addition, graphene was added to the cathode (LiMn₂O₄/graphene) to enhance the electronic conductivity. The synthesized LiMn₂O₄/graphene exhibited an ultrahigh-rate performance of 110.4 mAh·g^–1 at 50 C and an outstanding energy density at a high power density, maintaining 379.4 Wh·kg^–1 at 25,293 W·kg^–1. Besides, it shows durable stability, with only 0.02% decrease in the capacity per cycle at 10 C. Furthermore, the (LiMn₂O₄/graphene)/graphite full-cell exhibited a high discharge capacity. This work provides a promising method for the preparation of outstanding, integrated cathodes for potential applications in lithium ion batteries.

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An algebraic formulation of the simplex linear method for multiple integrals over the d-dimensional domain

We present the systematic treatment of multiple integrals over a simplex of the dimensionality d (d-simplex). The integrand is an analytical function in a suitable domain, and the linear form was employed as an argument. Using the elements obtained from the values of the integrand at the vertices of the d-simplex, integral can be evaluated analytically and expressed as the quotient of two determinants. Potential applications of the results described in the present study include numerical computations of Green?s function (GF), and the response of quantum systems in terms of complex susceptibilities in multidimensional space.     

Mechanical behavior and tensile/compressive strength asymmetry of ultrafine structured Ti–Nb–Ni–Co–Al alloys with bi-modal grain size distribution

Bulk ultrafine structured metallic materials with the bi-modal grain size distribution exhibit both high strength and good ductility. Here we show a new family of bi-modal Ti–Nb–Ni–Co–Al alloys. Their microstructure consists of an ultrafine structured eutectic matrix and relatively coarse β-Ti dendrites. Chemical modification of the parent Ti–Nb–Ni–Cu–Al system significantly affected type and volume fraction of matrix phases. In its turn, this influenced the deformation behavior. The unexpected “double yielding” behavior as well as tensile/compressive fracture strength asymmetry of the designed alloys are discussed in detail. For that, the microstructure alterations under compressive and tensile loading was in situ and ex situ analyzed by scanning electron microscopy.     

Effect of the temperature on surface modification of silica and properties of modified silica filled rubber composites

The modified silica at different temperature (MSaDT) with bis(3-triethoxysilylpropyl)tetrasulfide (TESPT), and MSaDT filled solution styrene butadiene rubber (SSBR) composites were prepared to investigate the effect of temperature on surface modification of silica. The results showed that TESPT was successfully bonded on the surface of silica by chemical bonds. The grafting degree (K) of MSaDT of 50 °C was 62.2% and higher than that at the other temperatures. The thermal weight loss and the size distribution of MSaDT showed that the silanol of TESPT hydrolysates reacted with the surface hydroxyl groups of silica, decreasing the average size and agglomeration of modified silica. For 50 °C modified silica/SSBR composite, the static mechanical properties and rubber–filler interaction of the composite were better than those of the others. As far as dynamic mechanical properties are concerned, the 50 °C modified silica/SSBR composite owned a best combination of low rolling resistance and high wet skid resistance.