车用塑料耐刮擦测试方法概述

耐刮擦测试是汽车内外饰塑料零件质量控制的一项重要指标。介绍了耐刮擦测试原理,刮擦头、负载、样品与刮擦头相对运动状态等是决定测试方法的关键技术要素,评价塑料耐刮擦性的方法分为目视法及仪器测量法。综述了五指刮擦法、硬度试验笔刮擦法、网格刮擦法、摩擦色牢度刮擦法及其他刮擦法测试方法,分析和总结了不同测试方法的特点和应用范围。     

无机硅酸盐涂料的研制及应用

以硅酸盐溶液为主要原料,利用少量自制的含偶联功能基团的有机硅聚合物乳液与硅酸盐进行杂化反应,同时与填料等有效的结合制备了无机硅酸盐涂料,并对涂料的性能进行研究。结果表明：制备的无机硅酸盐涂层具有优异的贮存稳定性、柔韧性、防水性、耐污性、阻燃性以及耐霉菌性等,满足建筑内外墙涂料的相关标准要求。     

Investigation of a Photochromic Diarylethene with Electron-acceptor Attached

In this contribution, an electron acceptor attached diarylethene derivative was synthesized and fully characterized. The photochromic behavior was investigated in THF. Under exposure of UV and visible light cycles, the solution color can be switched between colorless and yellow smoothly. Fatigue resistance measurements could be repeated 50 times with an acceptable degradation. Due to the electron acceptor attached to the framework of diarylethene, the photo- and thermal-stability were enhanced both. A full-photo mode switch can be established based on the well-defined states by external excitation. The molecular structures of ring-open and ring-closed form were optimized by Dmol³. The distance between photocyclizing atoms in aptiparallel conformation meets the requirement for photochromic reaction. And the calculated absorption wavelengths were also in agreement with the experimental values.     

聚合物锂离子电池界面相容性的研究进展

聚合物锂离子电池作为储能装置在电子产品中具有广泛的应用前景。电极/聚合物电解质(E/P)界面相容性是影响聚合物锂离子电池电导率、安全性、机械性能的重要影响因素之一。研究E/P界面的电化学反应及形成机理,是解决相容性问题的关键。本文综述了近年来有关聚合物锂离子电池E/P界面相容性及相关研究技术的进展,并对聚合物锂离子电池界面相容性的相关研究进行了展望。     

Qualitative spectroscopic characterization of the matrix–silane coupling agent interface across metal fibre reinforced ion exchange resin composite membranes

The characterization of novel metal reinforced electro-dialysis ion exchange membranes, for water desalination, by attenuated total reflectance Fourier transform infrared spectroscopy mapping is presented in this paper. The surface of the porous stainless steel fibre meshes was treated in order to enhance the amount of surface oxide groups and increase the material hydrophilicity. Then, the metal membranes were functionalized through a sol–gel reaction with silane coupling agents to enhance the affinity with the ion exchange resins and avoid premature metal oxidation due to redox reactions at the metal–polymer interface. Polished cross sections of the composite membranes embedded into an epoxy resin revealed interfaces between metallic frameworks and the silane layer at the interface with the ion exchange material. The morphology of the metal–polymer interface was investigated with scanning electron microscopy and Fourier transform infrared micro-spectroscopy. Fourier transform infrared mapping of the interfaces was performed using the attenuated total reflectance mode on the polished cross-sections at the Australian Synchrotron. The nature of the interface between the metal framework and the ion exchange resin was shown to be homogeneous and the coating thickness was found to be around 1 μm determined by Fourier transform infrared micro-spectroscopy mapping. The impact of the coating on the properties of the membranes and their potential for water desalination by electro-dialysis are also discussed.     

Facile synthesis of bio-based phosphorus-containing epoxy resins with excellent flame resistance

The development of high-performance biomass-derived epoxy thermosets with excellent flame resistance is vital to various applications (i.e., composites, coatings and adhesives). Herein, a difunctional epoxy monomer bis(2-methoxy-4-(oxiran-2-ylmethyl)phenyl) phenyl phosphate (BEU-EP) was synthesized from abundant and biobased eugenol. In addition, BEU-EP was cured by 4,4′-diaminodiphenyl methane (DDM) and the cured resin diglycidyl ether of bisphenol A (DGEBA)/DDM was used as a reference. Results indicated that BEU-EP/DDM not only showed a 58.1%, 28.8% and 35.1% increase in residual char (at 700 °C), flexural and storage modulus (at 30 °C) compared with DGEBA/DDM, but also exhibited excellent flame resistance and smoke suppression. BEU-EP/DDM passed V-0 rating (in UL-94 testing) with limiting oxygen index (LOI) of 38.4% and greatly decreased the peak heat release rate (pHRR) and total smoke production (TSP) by 84.9% and 80.5%, respectively. The mechanism analysis confirmed that the phosphorus-containing group and aromatic structure from BEU-EP contributed both the gas and condensed-phase flame retardation of BEU-EP/DDM network. This work provides an efficient and scalable route for synthesizing biobased epoxy thermosets with high integrated performance and superior flame resistance.     

Achieving highly crystalline rate and crystallinity in Poly(l-lactide) via in-situ melting reaction with diisocyanate and benzohydrazine to form nucleating agents

The drawback of the application for poly(_l-lactide) (PLLA) is the low crystalline rate and crystallinity obtaining via normal processing methods. Modifying crystallization of PLLA has been found to be an efficient way to improve its mechanical and heat resistance properties. In this wok, 4, 4′-diphenylmethane diisocyanate (M) and benzohydrazine (P) were employed into PLLA melt to in-situ form nucleating agents. The in-situ melting reaction was confirmed by a nuclear magnetic resonance spectroscopy. The crystallization behavior and crystalline morphology were investigated by a differential scanning calorimetry, a polarized optical microscopy and a field emission scanning electron microscope. The crystalline rate of PLLA was abruptly enhanced by adding (M+P) and melting reaction with PLLA. The crystallization half-time of PLLA dramatically decreased from 42.0 to 1.1 min at 130 °C by the in-situ formation of nucleating agents. The crystallinity of PLLA increased from 10.3 to 42.1 by adding 0.25% (M+P) and melting reaction for 8 min. Furthermore, the size of PLLA crystals was dramatically reduced because of the nucleating effect. Accompanied with improvement on crystallinity, the Vicat softening temperature of PLLA shifted from 57.4 °C to 93.7 °C by the in-situ reaction with 6.00% (M+P), and indicating heat resistance enhancement.     

Creep resistance of HDPE/PA66 system: Effect of PA66 phase geometry and graphite nanoplatelets addition

Microfibrillar composites (MFC) with in-situ generated short polymeric fibres feature, unlike composites containing inorganic rigid fibres/particles, lower creep resistance in comparison with analogous blends containing spheres. Further attribute is unprecedented decrease in creep resistance of the blend by graphite nanoplatelets (GNP). Explanation of this behaviour of the HDPE/PA66/GNP system consists in characterization of structure and finite element analysis (FEA) „mapping“ the effect of reinforcement and interface parameters on creep behaviour. Lowering of reinforcement modulus and its viscoelasticity may lead to worse creep resistance of fibrous composites. FEA also indicates marked negative effect of the soft interface, i.e. GNP-reduced crystallinity of HDPE near the interface, on creep resistance of the spheres-reinforced system in contrast to MFC. Structural changes are indicated by polarized light microscopy, SEM and TEM. The results reveal so far unknown complexity of the performance of polymer/polymer composites which may cause unprecedented antagonistic effects.     

Fabrication of flame-retardant and smoke-suppressant isocyanate-based polyimide foam modified by silica aerogel thermal insulation and flame protection layers

Because of containing urea groups, flame resistance and smoke releasing behaviors of isocyanate-based polyimide foam (IBPIF) produced using free foaming technology require further improvement. In this work, silica aerogel layers were incorporated into cells of IBPIF through an in situ growth process of silica sol (SS). Compared with silica aerogel particles directly mixed into the foaming slurry, the silica aerogel layers that firmly attached to the pores and surfaces of cells not only provided exceptional thermal insulation and flame protection, but also kept original cellular structure. With increase in ratio of SS mass to IBPIF volume, silica aerogel incorporation dosage was gradually increased. Accompanied by flame resistance was obviously improved and smoke releasing behavior was effectively suppressed. Those were indicated by the improved limiting oxygen index (LOI), decreased heat release rate (HRR), peak of HRR, and specific optical density of smoke (Ds) in trials with pilot flames. Compared with pure IBPIF, when the ratio reached to 5/15 g/cm³, it resulted in LOI increasing from 22.0% to 33.0%, peak of HRR, total smoke production (TSP), and maximum value of Ds decreasing from 174 to 72 kW/m², 1.11 to 0.37 m²/m², 45.90 to 17.45, respectively.