Self-healing and thermoreversible rubber from supramolecular assembly
Self-healing and thermoreversible rubber from supramolecular assembly
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DOI:
10.1038/nature06669
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发表时间:
2008-02-21
期刊:
影响因子:
64.8
通讯作者:
Leibler, Ludwik
中科院分区:
文献类型:
--
作者:
Cordier, Philippe;Tournilhac, Francois;Leibler, Ludwik
Rubbers exhibit enormous extensibility up to several hundred per cent, compared with a few per cent for ordinary solids, and have the ability to recover their original shape and dimensions on release of stress(1,2). Rubber elasticity is a property of macromolecules that are either covalently cross- linked(1,2) or connected in a network by physical associations such as small glassy or crystalline domains(3-5), ionic aggregates(6) or multiple hydrogen bonds(7-16). Covalent cross-links or strong physical associations prevent flow and creep. Here we design and synthesize molecules that associate together to form both chains and cross-links via hydrogen bonds. The system shows recoverable extensibility up to several hundred per cent and little creep under load. In striking contrast to conventional cross-linked or thermoreversible rubbers made of macromolecules, these systems, when broken or cut, can be simply repaired by bringing together fractured surfaces to self- heal at room temperature. Repaired samples recuperate their enormous extensibility. The process of breaking and healing can be repeated many times. These materials can be easily processed, re- used and recycled. Their unique self-repairing properties, the simplicity of their synthesis, their availability from renewable resources and the low cost of raw ingredients (fatty acids and urea) bode well for future applications.