Adaptable Crosslinks in Polymeric Materials: Resolving the Intersection of Thermoplastics and Thermosets

被引:709
作者
Scheutz, Georg M. [1 ]
Lessard, Jacob J. [1 ]
Sims, Michael B. [1 ]
Sumerlin, Brent S. [1 ]
机构
[1] Univ Florida, Dept Chem, George & Josephine Butler Polymer Res Lab, Ctr Macromol Sci & Engn, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
MOLECULAR-SIZE DISTRIBUTION; DYNAMIC COVALENT POLYMERS; STRESS-RELAXATION; VISCOELASTIC PROPERTIES; INVERSE VULCANIZATION; NETWORKS; VITRIMERS; CHEMISTRY; PERFORMANCE; GELATION;
D O I
10.1021/jacs.9b07922
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The classical division of polymeric materials into thermoplastics and thermosets based on covalent network structure often implies that these categories are distinct and irreconcilable. Yet, the past two decades have seen extensive development of materials that bridge this gap through incorporation of dynamic crosslinks, enabling them to behave as both robust networks and moldable plastics. Although their potential utility is significant, the growth of covalent adaptable networks (CANs) has obscured the line between "thermoplastic" and "thermo-set" and erected a conceptual barrier to the growing number of new researchers entering this discipline. This Perspective aims to both outline the fundamental theory of CANs and provide a critical assessment of their current status. We emphasize throughout that the unique properties of CANs emerge from the network chemistry, and particularly highlight the role that the crosslink exchange mechanism (i.e., dissociative exchange or associative exchange) plays in the resultant material properties under processing conditions. Predominant focus will be on thermally induced dynamic behavior, as the majority of presently employed exchange chemistries rely on thermal stimulus, and it is simple to apply to bulk materials. Lastly, this Perspective aims to identify current issues and address possible solutions for better fundamental understanding within this field.
引用
收藏
页码:16181 / 16196
页数:16
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