"一石三鸟 "战略,打造易于再加工的纤维素热固性树脂

IF 6.3 2区 化学 Q1 POLYMER SCIENCE
Tengfei Han , Yanshai Wang , Shufen Zhang , Benzhi Ju
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引用次数: 0

摘要

纤维素是最丰富的天然多糖,是替代石油基塑料的理想原料。然而,由于天然纤维素具有丰富而强烈的氢键相互作用,因此很难像传统塑料那样进行热加工。本研究利用纤维素的高碘酸盐氧化法制备了一系列纤维素的二醛衍生物(DAC),并以二季戊四醇作为 DAC 的交联剂,制备了基于缩醛动态共价键(ACC)的纤维素共价自适应网络。这种策略可以引入缩醛键、削弱氢键并降低刚性,一举三得。ACC 的出色再加工性能归功于乙缩醛键对纤维素氢键网络的重构,而乙缩醛键在高温下的可逆交换反应赋予了纤维素链以流动性,使得 ACC 可以在 90°C 下热压 15 分钟进行重塑。ACCs 具有出色的稳定性和可再加工性,有望取代目前不可再生的石油基塑料,并为开发其他类型的生物质塑料提供了灵感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

“Three birds with one stone” strategy for building easily reprocessable cellulosic thermosetting resins

“Three birds with one stone” strategy for building easily reprocessable cellulosic thermosetting resins
Cellulose is the most abundant natural polypolysaccharide and is an ideal raw material to replace petroleum-based plastics. However, natural cellulose is difficult to be thermo-processed like conventional plastics because of the rich and strong hydrogen bonds interactions. In this study, a series of dialdehyde derivatives of cellulose (DACs) were prepared by periodate oxidation of cellulose, and cellulose covalent adaptive networks based on acetal dynamic covalent bonds (ACCs) were prepared using dipentaerythritol as a crosslinker for DAC. This strategy can introduce acetal bonds, weaken hydrogen bonds, and reduce rigidity to kill three birds with one stone. The excellent reprocessing performance of ACCs is attributed to the reconstruction of the cellulose hydrogen bond network by acetal bonds, and the reversible exchange reaction of the acetal bonds at high temperatures endows the cellulose chains with mobility, allowing ACCs to be remodeled by hot pressing at 90°C for 15 min. The excellent stability and reprocessability of ACCs hold the promise of replacing current non-renewable petroleum-based plastics and provide inspiration for the development of other types of biomass plastics.
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来源期刊
Polymer Degradation and Stability
Polymer Degradation and Stability 化学-高分子科学
CiteScore
10.10
自引率
10.20%
发文量
325
审稿时长
23 days
期刊介绍: Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology. Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal. However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.
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