TY - JOUR
T1 - Arresting Elevated-Temperature Creep and Achieving Full Cross-Link Density Recovery in Reprocessable Polymer Networks and Network Composites via Nitroxide-Mediated Dynamic Chemistry
AU - Li, Lingqiao
AU - Chen, Xi
AU - Jin, Kailong
AU - Rusayyis, Mohammed Bin
AU - Torkelson, John M.
N1 - Funding Information:
We acknowledge support of Northwestern University via discretionary funds associated with a Walter P. Murphy Professorship (J.M.T.), ISEN Fellowships (L.L.; X.C.), Terminal-Year Fellowships (L.L.; X.C.; K.J.), and a 3M Fellowship (X.C.). We thank Prof. L. C. Brinson for generously providing access to DMA equipment and Dr. Paul Endres from Goodyear for generously providing the TSR-10, the blend of TSR-10 with high MW PB, and the TSR-10 that was well mixed with 33 wt % CB.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/2/9
Y1 - 2021/2/9
N2 - Thermosets and thermoset composites constitute an extraordinary challenge for recycling and participation in a circular economy because their permanent covalent cross-links prevent spent thermosets from being melt processed into new products. With annual world-wide production in the tens of billions of kilograms, the inability to recycle thermosets into high-value products represents major economic and sustainability losses. While recent research into polymer networks with dynamic covalent cross-links has indicated promise for reprocessability at common melt-state processing temperatures, a crucial shortcoming has been identified: such reprocessable networks and network composites commonly exhibit creep at use conditions due to their dynamic nature, which may prevent their use in applications that require long-term dimensional stability. Here, we use a strategy based on nitroxide-mediated polymerization to synthesize reprocessable networks and network composites containing alkoxyamine dynamic bonds. The resulting networks, including those synthesized from lab-grade polybutadiene and industrial-grade natural rubber/carbon black composites, exhibit full cross-link density recovery and essentially no creep at 80 °C, where alkoxyamine cross-links are nearly static, after multiple molding cycles at 140/160 °C, where alkoxyamine cross-links are dynamic. This capability to "turn on"and "arrest"dynamic chemistry over a relatively narrow temperature window is attributed to the high activation energy (∼120 kJ/mol) and thus strong temperature dependence of the alkoxyamine dissociation reaction. With this key element of high activation energy for the dissociation reaction in systems undergoing dynamic reversion or the dynamic exchange reaction in vitrimers, it is possible to design covalent network materials with acute temperature response allowing for reprocessability with outstanding elevated-temperature creep resistance.
AB - Thermosets and thermoset composites constitute an extraordinary challenge for recycling and participation in a circular economy because their permanent covalent cross-links prevent spent thermosets from being melt processed into new products. With annual world-wide production in the tens of billions of kilograms, the inability to recycle thermosets into high-value products represents major economic and sustainability losses. While recent research into polymer networks with dynamic covalent cross-links has indicated promise for reprocessability at common melt-state processing temperatures, a crucial shortcoming has been identified: such reprocessable networks and network composites commonly exhibit creep at use conditions due to their dynamic nature, which may prevent their use in applications that require long-term dimensional stability. Here, we use a strategy based on nitroxide-mediated polymerization to synthesize reprocessable networks and network composites containing alkoxyamine dynamic bonds. The resulting networks, including those synthesized from lab-grade polybutadiene and industrial-grade natural rubber/carbon black composites, exhibit full cross-link density recovery and essentially no creep at 80 °C, where alkoxyamine cross-links are nearly static, after multiple molding cycles at 140/160 °C, where alkoxyamine cross-links are dynamic. This capability to "turn on"and "arrest"dynamic chemistry over a relatively narrow temperature window is attributed to the high activation energy (∼120 kJ/mol) and thus strong temperature dependence of the alkoxyamine dissociation reaction. With this key element of high activation energy for the dissociation reaction in systems undergoing dynamic reversion or the dynamic exchange reaction in vitrimers, it is possible to design covalent network materials with acute temperature response allowing for reprocessability with outstanding elevated-temperature creep resistance.
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U2 - 10.1021/acs.macromol.0c01691
DO - 10.1021/acs.macromol.0c01691
M3 - Article
AN - SCOPUS:85099795465
SN - 0024-9297
VL - 54
SP - 1452
EP - 1464
JO - Macromolecules
JF - Macromolecules
IS - 3
ER -