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Vinyl-terminated benzoxazine (VB-a), which can be polymerized through ring-opening polymerization, was synthesized through the Mannich condensation of bisphenol A, formaldehyde, and allylamine. This VB-a monomer was then blended with epoxy resin and then concurrently thermally cured to form an epoxy/VB-a copolymer network. To understand the curing kinetics of this epoxy/VB-a copolymer, dynamic differential scanning calorimetry measurements were performed by the Kissinger and Flynn-Wall-Ozawa methods. Fourier transform infrared (FTIR) analyses revealed the presence of thermal curing reactions and hydrogen-bonding interactions of the epoxy/VB-a copolymers. Meanwhile, a significant enhancement of the ring-opening and allyl polymerizations of the epoxy was observed. For these interpenetrating polymer networks, dynamic mechanical analysis and thermogravimetric analysis results indicate that the thermal properties increased with increasing VB-a content in the epoxy/VB-a copolymers.

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In this work, titanium nitride (TiN) nanorod arrays were fabricated using glancing angle deposition in a magnetron sputtering system. The deposition parameters, including the bias on the substrate and the flow rate of nitrogen, were varied to deposit various TiN nanorod arrays. Before glancing angle deposition was conducted, uniform TiN films were deposited and their permittivity spectra, for various deposition parameters, were obtained. The effect of the deposition parameters on the morphology of the nanorods is analyzed here. The polarization-dependent extinctance spectra of TiN nanorod arrays were measured and compared. Extinction, which corresponds to the longitudinal mode of localized surface plasmon resonance, can be significantly changed by tuning the N2 flow rate and substrate bias voltage during deposition.

Differential scanning calorimetry, one-and two-dimensional Fourier transform infrared (FTIR), and solid state nuclear magnetic resonance (NMR) spectroscopy have been used to investigate the miscibility of and specific interactions between poly(styrene-co-vinyl phenol) (PSOH) and poly(3-hydroxybutyrate) (PHB) upon varying the vinyl phenol content of the PSOH copolymer. The FTIR and solid state NMR spectra revealed that the phenol units of PVPh interact with the carbonyl groups of PHB through intermolecular hydrogen bonding. A miscibility window exists when the vinyl phenol fraction in the copolymer is greater than 22 mol % in the PSOH/PHB blend system, as predicted using the Painter-Coleman association model.