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Bio-composites materials from engineered natural fibres for structural applications

机译:工程天然纤维的生物复合材料,用于结构应用

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摘要

The large environmental footprint caused by conventional synthetic fibre reinforced petrochemical-derived polymer composites along with potential improvement in mechanical properties for natural fibre reinforced bio-derived polymer composites, have long been a motivation for further research and innovation in natural fibre composites. Harakeke and hemp fibres, amongst other natural fibres, possess respectable mechanical properties along with other advantages such as low cost, low production energy requirements and abundant availability. Polylactic acid (PLA), a sustainable alternative to petrochemical-derived polymers, is produced on a mass scale from 100% renewable resources and can be degraded at end of life by simple hydrolysis under the appropriate conditions. It has high stiffness, strength, thermal and UV stability, but is low in toughness. Limited applications of natural fibre reinforced PLA composites so far is mainly due to low mechanical properties of discontinuous fibre composites made using injection moulding or compression moulding using randomly oriented fibre mats attributed to poor fibre orientation and fibre-matrix incompatibility. Presented in this study are experimental investigations of the properties of PLA reinforced aligned discontinuous harakeke and hemp fibre mats produced using a dynamic sheet former (DSF) to provide improved performance of discontinuous fibre composites.Harakeke and hemp fibres were treated using either a solution of 5 wt% or 10 wt% NaOH or combination of 5 wt% NaOH with 2 wt% Na2SO3 at elevated temperatures in a small pressure vessel. Treated fibres were assessed using single fibre tensile testing, X-ray diffraction (XRD), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). It was found that 5 wt% NaOH/2 wt% Na2SO3 and 5 wt% NaOH effectively removed non-cellulosic materials from harakeke and hemp fibre surfaces, respectively, giving good fibre separation without greatly reducing the tensile strength of the fibres. It was also found that these treatments lead to a higher crystallinity index and improved thermal stability of fibres.Fibre alignment in fibre mats produced using a DSF was observed using light microscopy. Visual observation supported that the fibre alignment had occurred. Fibre orientation factors (Kɵ) determined for harakeke and hemp composites using the Bowyer-Bader model were found higher compared to Kɵ values obtained for other natural composites prepared using injection and compression moulding. Improved fibre orientation resulted in improved reinforcement giving large increases for tensile strengths up to approximately 90 and 60% for harakeke and hemp composites reinforced with inclusion of 30 and 25 wt% fibre respectively. The effect of silane and peroxide as additional fibre treatments and MA-g-PLA as a coupling agent was evaluated by scanning electron microscopy (SEM), composite swelling analysis, tensile testing, dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA). Scanning electron micrographs of fractured composite surfaces revealed that the gaps between fibres and matrix for composites with fibres treated using silane and peroxide and composites coupled with MA-g-PLA were smaller compared to the surfaces for composites with fibres treated using just alkali. Improved interfacial strength was also supported by lower swelling indices, lower peaks on tan δ and higher residual composites weights, compared to those values obtained for composites with fibres treated using just alkali, which was found to lead to higher composite tensile strengths.Harakeke and hemp fibre composites were plasticised using hyper-branched polymer (HBP) and assessed using SEM, tensile and impact testing. SEM micrographs for plasticised composites revealed longer pultruding fibres than un-plasticised composites, with gaps between the fibre and matrix appearing to be slightly larger, indicating a weaker interface between fibres and matrix compared to those composites without plasticiser. Improved composite ductility and impact strength were demonstrated for plasticised composites without dramatic reduction of composite tensile strength.
机译:常规合成纤维增强的石油化学衍生的聚合物复合材料引起的巨大环境足迹,以及天然纤维增强的生物衍生的聚合物复合材料的机械性能的潜在改善,长期以来一直是对天然纤维复合材料进行进一步研究和创新的动力。除其他天然纤维外,Harakeke和大麻纤维还具有可观的机械性能以及其他优势,例如成本低,生产能量需求低和可用性高。聚乳酸(PLA)是石油化工衍生的聚合物的可持续替代品,是由100%可再生资源大规模生产的,可以在适当的条件下通过简单的水解作用在使用寿命结束时降解。它具有高的刚度,强度,热和紫外线稳定性,但韧性低。迄今为止,天然纤维增强的PLA复合材料的有限的应用主要是由于不连续的纤维复合材料的机械性能低,该不连续的纤维复合材料是使用随机取向的纤维毡通过注射成型或压缩成型制成的,这归因于不良的纤维取向和纤维-基质不相容性。本研究介绍了使用动态成膜剂(DSF)生产的PLA增强排列的不连续harakeke和大麻纤维毡的性能的实验研究,以改善不连续纤维复合材料的性能。使用5种溶液处理Harakeke和大麻纤维wt%或10 wt%的NaOH或5 wt%的NaOH与2 wt%的Na2SO3的组合在小型压力容器中在高温下进行。使用单纤维拉伸试验,X射线衍射(XRD),扫描电子显微镜(SEM)和热重分析(TGA)评估处理过的纤维。发现5重量%的NaOH / 2重量%的Na 2 SO 3和5重量%的NaOH分别有效地从harakeke和大麻纤维表面去除了非纤维素材料,从而提供了良好的纤维分离,而没有大大降低纤维的拉伸强度。还发现这些处理导致更高的结晶度指数和改进的纤维热稳定性。使用光学显微镜观察到使用DSF生产的纤维垫中的纤维排列。视觉观察支持发生纤维对准。发现使用Bowyer-Bader模型确定的harakeke和大麻复合材料的纤维取向因子(Kɵ)高于使用注塑和压塑法制备的其他天然复合材料的Kɵ值。改善的纤维取向导致改善的增强,使分别含有30%和25%的纤维增强的harakeke和大麻复合材料的抗张强度大幅度提高,达到了大约90%和60%。通过扫描电子显微镜(SEM),复合材料溶胀分析,拉伸试验,动态力学分析(DMA)和热重分析(TGA)评估了硅烷和过氧化物作为其他纤维处理剂和MA-g-PLA作为偶联剂的效果。断裂的复合材料表面的扫描电子显微照片显示,与仅使用碱处理的纤维复合材料的表面相比,使用硅烷和过氧化物处理的纤维复合材料以及与MA-g-PLA偶联的复合材料的纤维和基质之间的间隙较小。与仅用碱处理的纤维复合材料获得的那些值相比,较低的溶胀指数,较低的tanδ峰和较高的复合材料残余重量也支持了界面强度的改善,从而发现了较高的复合材料抗张强度。纤维复合材料使用超支化聚合物(HBP)进行增塑,并使用SEM,拉伸和冲击测试进行评估。增塑复合材料的SEM显微照片显示,拉挤纤维比未增塑复合材料更长,纤维与基质之间的间隙似乎稍大,这表明与未加增塑剂的复合材料相比,纤维与基质之间的界面更弱。在不显着降低复合材料拉伸强度的情况下,已证明了增塑复合材料的复合材料延展性和冲击强度得到改善。

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    Mohd Ghazali Aruan Efendy;

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  • 年度 2016
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  • 原文格式 PDF
  • 正文语种 en
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