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Thermal forming of chemically modified wood to make high-performance plastic-like wood composites

机译:化学改性木材的热成型,以制造高性能的类塑料木材复合材料

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Chemically modified wood composites were obtained via the compression moulding of thermoplasticised Aspen (Populus tremula) sawdust. This sawdust was previously prepared by esterification with maleic anhydride (MA) and subsequent oligoesterification with maleic anhydride and glycidyl methacrylate (GMA). The thermoplastic properties of the chemically modified wood resulting from different modification procedures were confirmed and compared by compression-moulding experiments leading to preliminary and final products. An SEM study of the resulting products clearly showed that the oligo-esterified wood had partially melted under pressure and temperature, such that the overlapping and surface melting of particles ensured adhesive bonding between those particles. A new type of wood/thermoplastic-wood composite was obtained. In these composites, the melted part of the modified wood plays the role of the cohesive matrix whilst none-melted wood remains as a fibrous reinforcing material. FTIR spectra suggested that changes in the chemical structure of the modified wood are possible during the thermal forming process (e.g. polymerisation of C= C double bonds). The final composites were yellowish-brown, glossy, plastic-like products that showed interesting physical, mechanical and biological properties. They are water-resistant and dimensionally stable and display good electrical insulating behaviour. Their mechanical properties (bending strength of ca. 64 MPa and tensile strength of ca. 36 MPa) are in the typical range for plastics and conventional wood-fibre/plastic composites, and are superior to common wood products such as fibreboards and particleboards. Furthermore, the outstandingly high internal bond (ca. 3.0 MPa) highlights the totally different adhesion mechanism operating in these new types of composites. Although the novel composites are much more resistant to decay than the original unmodified wood, they remain ultimately biodegradable plastic-like composites.
机译:化学改性的木材复合材料是通过对热塑性白杨木(Populus tremula)锯末进行压缩成型而获得的。该锯末事先通过与马来酸酐(MA)酯化,随后与马来酸酐和甲基丙烯酸缩水甘油酯(GMA)进行低酯化制备。由不同的改性程序得到的化学改性木材的热塑性特性得到了确认,并通过模压实验进行了比较,从而得到了初级和最终产品。对所得产物的SEM研究清楚地表明,低酯化的木材在压力和温度下已经部分熔融,因此颗粒的重叠和表面熔融确保了这些颗粒之间的粘合。获得了一种新型的木材/热塑性-木材复合材料。在这些复合材料中,改性木材的熔融部分起着粘结基质的作用,而没有熔融的木材则保留为纤维增强材料。 FTIR光谱表明,改性木的化学结构可能在热成型过程中发生变化(例如C = C双键的聚合)。最终的复合材料是黄褐色,有光泽的塑料状产品,显示出令人感兴趣的物理,机械和生物学特性。它们具有防水性和尺寸稳定性,并具有良好的电绝缘性能。它们的机械性能(抗弯强度约为64 MPa,抗张强度约为36 MPa)在塑料和常规木纤维/塑料复合材料的典型范围内,并且优于常见的木制品,例如纤维板和刨花板。此外,出色的高内部粘合力(约3.0 MPa)突显了这些新型复合材料中完全不同的粘合机理。尽管新型复合材料比原始的未改性木材具有更强的抗腐性,但它们最终仍是可生物降解的类塑料复合材料。

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