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      Catalyst-free room-temperature self-healing elastomers based on aromatic disulfide metathesis

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          A thermally re-mendable cross-linked polymeric material.

          We have developed a transparent organic polymeric material that can repeatedly mend or "re-mend" itself under mild conditions. The material is a tough solid at room temperature and below with mechanical properties equaling those of commercial epoxy resins. At temperatures above 120 degrees C, approximately 30% (as determined by solid-state nuclear magnetic resonance spectroscopy) of "intermonomer" linkages disconnect but then reconnect upon cooling, This process is fully reversible and can be used to restore a fractured part of the polymer multiple times, and it does not require additional ingredients such as a catalyst, additional monomer, or special surface treatment of the fractured interface.
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            Metal-catalyzed transesterification for healing and assembling of thermosets.

            Catalytic control of bond exchange reactions enables healing of cross-linked polymer materials under a wide range of conditions. The healing capability at high temperatures is demonstrated for epoxy-acid and epoxy-anhydride thermoset networks in the presence of transesterification catalysts. At lower temperatures, the exchange reactions are very sluggish, and the materials have properties of classical epoxy thermosets. Studies of model molecules confirmed that the healing kinetics is controlled by the transesterification reaction rate. The possibility of varying the catalyst concentration brings control and flexibility of welding and assembling of epoxy thermosets that do not exist for thermoplastics.
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              Self-healing polymeric materials: A review of recent developments

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                Author and article information

                Journal
                MHAOAL
                Mater. Horiz.
                Mater. Horiz.
                Royal Society of Chemistry (RSC)
                2051-6347
                2051-6355
                2014
                2014
                : 1
                : 2
                : 237-240
                Article
                10.1039/C3MH00061C
                850461ad-c91a-4c05-9fba-e391fee4c039
                © 2014
                History

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