Guerre Marc, Taplan Christian, Winne Johan M, Du Prez Filip E
Laboratoire des IMRCP, Université de Toulouse, CNRS UMR5623, Université Paul Sabatier 118 route de Narbonne 31062 Toulouse Cedex 9 France
Department of Organic and Macromolecular Chemistry, Polymer Chemistry Research Group, Center of Macromolecular Chemistry (CMaC), Faculty of Sciences, Ghent University Krijgslaan 281 (S4-bis) 9000 Ghent Belgium
Chem Sci. 2020 Apr 16;11(19):4855-4870. doi: 10.1039/d0sc01069c.
The development of more sustainable materials with a prolonged useful lifetime is a key requirement for a transition towards a more circular economy. However, polymer materials that are long-lasting and highly durable also tend to have a limited application potential for re-use. This is because such materials derive their durable properties from a high degree of chemical connectivity, resulting in rigid meshes or networks of polymer chains with a high intrinsic resistance to deformation. Once such polymers are fully synthesised, thermal (re)processing becomes hard (or impossible) to achieve without damaging the degree of chemical connectivity, and most recycling options quickly lead to a drop or even loss of material properties. In this context, both academic and industrial researchers have taken a keen interest in materials design that combines high degrees of chemical connectivity with an improved thermal (re)processability, mediated through a dynamic exchange reaction of covalent bonds. In particular vitrimer materials offer a promising concept because they completely maintain their degree of chemical connectivity at all times, yet can show a clear thermally driven plasticity and liquid behavior, enabled through rapid bond rearrangement reactions within the network. In the past decade, many suitable dynamic covalent chemistries were developed to create vitrimer materials, and are now applicable to a wide range of polymer matrices. The material properties of vitrimers, however, do not solely rely on the chemical structure of the polymer matrix, but also on the chemical reactivity of the dynamic bonds. Thus, chemical reactivity considerations become an integral part of material design, which has to take into account for example catalytic and cross-reactivity effects. This mini-review will aim to provide an overview of recent efforts aimed at understanding and controlling dynamic cross-linking reactions within vitrimers, and how directing this chemical reactivity can be used as a handle to steer material properties. Hence, it is shown how a focus on a fundamental chemical understanding can pave the way towards new sustainable materials and applications.
开发具有更长使用寿命的更可持续材料是向更循环经济转型的关键要求。然而,持久且高度耐用的聚合物材料在再利用方面的应用潜力往往也很有限。这是因为此类材料的耐用性能源于高度的化学连接性,从而形成具有高固有抗变形能力的刚性聚合物链网或网络。一旦此类聚合物完全合成,在不破坏化学连接程度的情况下进行热(再)加工就变得困难(或不可能),而且大多数回收选项很快会导致材料性能下降甚至丧失。在这种背景下,学术和工业研究人员都对材料设计产生了浓厚兴趣,这种设计通过共价键的动态交换反应将高度的化学连接性与改善的热(再)加工性相结合。特别是玻璃态弹性体材料提供了一个很有前景的概念,因为它们在任何时候都能完全保持其化学连接程度,但又能通过网络内的快速键重排反应表现出明显的热驱动可塑性和液体行为。在过去十年中,人们开发了许多合适的动态共价化学方法来制备玻璃态弹性体材料,并且这些方法现在可应用于广泛的聚合物基体。然而,玻璃态弹性体的材料性能不仅取决于聚合物基体的化学结构,还取决于动态键的化学反应性。因此,化学反应性考量成为材料设计的一个组成部分,这必须考虑例如催化和交叉反应效应等因素。本综述旨在概述近期为理解和控制玻璃态弹性体内的动态交联反应所做的努力,以及如何利用这种化学反应性的导向作用来调控材料性能。因此,展示了专注于基本化学理解如何能为新型可持续材料及应用铺平道路。