Dolçà Celia, Fages Eduardo, Gonga Eloi, Garcia-Sanoguera David, Balart Rafael, Quiles-Carrillo Luis
Textile Industry Research Association (AITEX), Plaza Emilio Sala, 1, 03801 Alcoy, Spain.
Technological Institute of Materials (ITM), Universitat Politècnica de València (UPV), Plaza Ferrándiz y Carbonell, 1, 03801 Alcoy, Spain.
Polymers (Basel). 2021 Dec 30;14(1):138. doi: 10.3390/polym14010138.
Biobased HDPE (bioHDPE) was melt-compounded with different percentages (2.5 to 40.0 wt.%) of short hemp fibers (HF) as a natural reinforcement to obtain environmentally friendly wood plastic composites (WPC). These WPC were melt-compounded using a twin-screw extrusion and shaped into standard samples by injection molding. To improve the poor compatibility between the high non-polar BioHDPE matrix and the highly hydrophilic lignocellulosic fibers, a malleated copolymer, namely, polyethylene--maleic anhydride (PE-g-MA), was used. The addition of short hemp fibers provided a remarkable increase in the stiffness that, in combination with PE-g-MA, led to good mechanical performance. In particular, 40 wt.% HF drastically increased the Young's modulus and impact strength of BioHDPE, reaching values of 5275 MPa and 3.6 kJ/m, respectively, which are very interesting values compared to neat bioHDPE of 826 MPa and 2.0 kJ/m. These results were corroborated by dynamic mechanical thermal analysis (DMTA) results, which revealed a clear increasing tendency on stiffness with increasing the fiber loading over the whole temperature range. The crystal structure was not altered by the introduction of the natural fibers as could be seen in the XRD patterns in which mainly the heights of the main peaks changed, and only small peaks associated with the presence of the fiber appeared. Analysis of the thermal properties of the composites showed that no differences in melting temperature occurred and the non-isothermal crystallization process was satisfactorily described from the combined Avrami and Ozawa model. As for the thermal degradation, the introduction of HF resulted in the polymer degradation taking place at a higher temperature. As for the change in color of the injected samples, it was observed that the increase in fiber generated a clear modification in the final shades of the pieces, reaching colors very similar to dark woods for percentages higher than 20% HF. Finally, the incorporation of an increasing percentage of fibers also increased water absorption due to its lignocellulosic nature in a linear way, which drastically improved the polarity of the composite.
生物基高密度聚乙烯(bioHDPE)与不同百分比(2.5至40.0重量%)的短麻纤维(HF)进行熔融共混,作为天然增强材料,以获得环保型木塑复合材料(WPC)。这些WPC通过双螺杆挤出进行熔融共混,并通过注塑成型制成标准样品。为了改善高非极性BioHDPE基体与高亲水性木质纤维素纤维之间较差的相容性,使用了一种马来酸化共聚物,即聚乙烯-马来酸酐(PE-g-MA)。短麻纤维的添加显著提高了刚度,与PE-g-MA结合,导致了良好的机械性能。特别是,40重量%的HF极大地提高了BioHDPE的杨氏模量和冲击强度,分别达到5275 MPa和3.6 kJ/m,与纯bioHDPE的826 MPa和2.0 kJ/m相比,这些值非常可观。动态机械热分析(DMTA)结果证实了这些结果,该结果表明在整个温度范围内,随着纤维含量的增加,刚度呈明显增加趋势。如XRD图谱所示,天然纤维的引入并未改变晶体结构,其中主要是主峰高度发生变化,仅出现了与纤维存在相关的小峰。对复合材料热性能的分析表明,熔点温度没有差异,并且结合Avrami和Ozawa模型能够令人满意地描述非等温结晶过程。至于热降解,HF的引入导致聚合物在更高温度下发生降解。至于注塑样品颜色的变化,观察到纤维含量的增加使制品的最终色调发生了明显变化,对于HF含量高于20%的情况,颜色与深色木材非常相似。最后,由于其木质纤维素性质,纤维含量的增加也以线性方式增加了吸水率,这极大地改善了复合材料的极性。