Controlling phase separation in polymer systems has shown significant promise in combining properties of different components into an integrated polymer system. In this work, we investigate the effect of photoinduced phase separation on polymer morphology and properties in hybrid radical/cationic systems composed of butyl acrylate (BA) and difunctional oxetane (DOX). We show that the irradiation intensity has a significant effect on the formation of phase-separated domains. By increasing the irradiation intensity at fixed co-monomer composition, the morphology changes from one with a continuous soft BA domain to one with co-continuous BA (soft) and DOX (hard) domains. At higher irradiation intensity, the domain size of each phase is decreased because of fast photopolymerization, which significantly limits monomer/polymer diffusion. The smaller domain size enhances the flexibility and strength of the phase-separated polymers. On the other hand, the irradiation intensity has little to no effect on the polymer structure or properties for systems that do not phase-separate. Dynamic mechanical analysis demonstrates that phase separation associated with higher irradiation intensity during cure contributes to a 40-fold increase in toughness and up to fivefold higher elongation at break. This behavior is attributed to the formation of polymers with co-continuous hard/soft domains and decreased domain size. This study demonstrates that the morphology and properties of photoinduced phase-separated materials can be controlled by altering the initiation irradiation intensity for hybrid radical/cationic materials.

Cationic photopolymerization has become increasingly important in thin-film applications for advantages including no oxygen inhibition and rapid polymerization rates. Photocurable cationic thin film properties are often modulated by incorporation of oligomeric and prepolymer materials, but little work has directly examined the effect of prepolymer structure and reactive group placement on the thermomechanical properties of the final material. To explore the role of molecular architecture, epoxy functionalized butyl acrylate gradient copolymers were synthesized with reactive groups in end segments or randomly distributed along the prepolymer chain. Polymerized end functionalized formulations exhibit moduli almost double that of random functionalized oligomer formulations. In addition, inclusion of end functionalized prepolymers decreases creep of resulting thin films by a factor of 10. Furthermore, decreasing the concentration of the cross-linking diluent in end functionalized prepolymer systems results in amorphous networks with significantly lower mechanical strength. Increasing reactive groups at the ends of prepolymers produces stronger materials without affecting tensile elongation at break. These properties indicate that the structured oligomers facilitate the formation of continuous hard domains with high cross-link density with inclusions of soft, flexible domains of low cross-link density. This study demonstrates that the prepolymer architecture governs network formation and ultimate properties. V C 2016 Wiley Periodicals, Inc. J.

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Most sense organs of arthropods are ensconced in small exoskeletal compartments that hinder direct access to plasma membranes. We have developed a method for exposing live sensory and supporting cells in such structures. The technique uses a viscous light cured resin to embed and support the structure, which is then sliced with a sharp blade. We term the procedure a "goggatomy," from the Khoisan word for a bug, gogga. To demonstrate the utility of the method we show that it can be used to expose the auditory chordotonal organs in the second antennal segment and the olfactory receptor neurons in the third antennal segment of Drosophila melanogaster, preserving the transduction machinery. The procedure can also be used on other small arthropods, like mosquitoes and mites to expose a variety of cells.