4.7 Article

Fracture Toughness of Polymer Interfaces Compatibilized with Nanoparticle Brushes

Journal

MACROMOLECULES
Volume 55, Issue 12, Pages 4937-4946

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.2c00640

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Funding

  1. National Science Foundation [DMR-2124814]

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Surface-active particles can enhance the stability of immiscible polymer/polymer interfaces, but they may compromise the fracture toughness of the interfaces. By grafting silica nanoparticles with poly(styrene-r-methyl methacrylate) and utilizing the entanglement mechanism between the grafts and homopolymers, a particle-based system with improved fracture toughness is designed.
Surface-active particles at immiscible polymer/ polymer interfaces can provide unparalleled stability against droplet coalescence. However, they often deteriorate the fracture toughness (Gc) of the interface because their rigid cores act as stress concentrators. Here, we draw on the knowledge developed for the interfacial strengthening mechanisms of block and random copolymers to design analogous particle-based systems. We use silica nanoparticles grafted-from with poly(styrene-r-methyl interfaces. In this manner, the silica cores suppress droplet coalescence, while the PS-r-PMMA grafts entangle with the homopolymers and transmit stress across the interface. Interestingly, we show that Gc for the interfaces compatibilized with these particle brushes can exceed that of the interfaces compatibilized with ungrafted copolymer analogues. Rheology experiments attribute this phenomenon to increased connectivity between the entanglement points in these hybrid particle brush systems.

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