Carbodiimide-fueled anhydride bond formation has been used to enhance the mechanical properties of permanently crosslinked polymer networks, giving materials that exhibit transitions from soft gels to covalently reinforced gels, eventually returning to the original soft gels. Temporary changes in mechanical properties result from a transient network of anhydride crosslinks, which eventually dissipate by hydrolysis. Over an order of magnitude increase in the storage modulus is possible through carbodiimide fueling. The time-dependent mechanical properties can be modulated by the concentration of carbodiimide, temperature, and primary chain architecture. Because the materials remain rheological solids, new material functions such as temporally controlled adhesion and rewritable spatial patterns of mechanical properties have been realized.

Carbodiimide-fueled anhydride bond formation has been used to enhance the mechanical properties of permanently crosslinked polymer networks, giving materials that exhibit gel-gel-gel transitions. Temporary changes in mechanical properties result from a transient network of anhydride crosslinks which eventually dissipate by hydrolysis. Over an order of magnitude increase in storage modulus is possible through carbodiimide fueling. The time-dependent mechanical properties could be modulated by the concentration of carbodiimide, temperature, and primary chain architecture. Because the materials remain rheological solids, applications such as temporally controlled adhesives and rewritable spatial patterns of mechanical properties are possible.