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首页> 外文期刊>Nature Materials >Environmentally degradable,high-performance thermoplastics from phenolic phytomonomers
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Environmentally degradable,high-performance thermoplastics from phenolic phytomonomers

机译:酚类植物单体的环保可降解高性能热塑性塑料

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Aliphatic polyesters,such as poly(lactic acid),which degrade by hydrolysis,from naturally occurring molecules form the main components of biodegradable plastics'.However,these polyesters have become substitutes for only a small percentage of the currently used plastic materials because of their poor thermal and mechanical properties.Polymers that degrade into natural molecules and have a performance closer to that of engineering plastics would be highly desirable.Although the use of a high-strength filler such as a bacterial cellulose or modified lignin greatly increases the plastic properties,it is the matrix polymer that determines the intrinsic properties of the composite.The introduction of an aromatic component into the thermoplastic polymer backbone is an efficient method to intrinsically improve the material performance.Here,we report the preparation of environmentally degradable,liquid crystalline,wholly aromatic polyesters.The polyesters were derived from polymerizable plant-derived chemicals-in other words,'phytomonomers' that are widely present as lignin biosynthetic precursors.The mechanical performance of these materials surpasses that of current biodegradable plastics,with a mechanical strength,sigma,of 63 MPa,a Young's modulus,E,of 16 GPa,and a maximum softening temperature of 169 deg C.On light irradiation,their mechanical properties improved further and the rate of hydrolysis accelerated.
机译:从天然分子中水解而降解的脂肪族聚酯,例如聚乳酸,构成了生物可降解塑料的主要成分。但是,由于它们的存在,这些聚酯仅能替代少量的目前使用的塑料热和机械性能差。降解为天然分子并具有更接近工程塑料性能的聚合物是非常理想的。尽管使用高强度填料,例如细菌纤维素或改性木质素可以大大提高塑料的性能,正是基体聚合物决定了复合材料的固有性能。在热塑性聚合物主链中引入芳族组分是一种本质上改善材料性能的有效方法。在此,我们报道了可环境降解的液晶的制备芳族聚酯。聚酯衍生自可聚合植物提取出的化学物质,即作为木质素生物合成前体而广泛存在的“植物单体”。这些材料的机械性能超过了目前的可生物降解塑料,其机械强度σ为63 MPa,杨氏模量E为16 GPa,最高软化温度169℃。在光照射下,它们的机械性能进一步提高,水解速度加快。

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  • 来源
    《Nature Materials 》 |2006年第12期| p.966-970| 共5页
  • 作者单位

    Present address: School of Materials Science,Japan Advanced Institute of Science and Technology,1 -1,Asahidai,Nomi 923-1292,Japan;

    Department of Applied Chemistry,Graduate School of Engineering,Osaka University,2-1,Yamadaoka,Suita 565-0871,Japan;

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  • 正文语种 eng
  • 中图分类 工程材料学 ;
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