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Brian C Benicewicz

Publications and source records attributed to Brian C Benicewicz.

2 recordsLinked to original sources

The effect of tetrahydrofuran as solvent on matrix-assisted laser desorption/ionization and electrospray ionization mass spectra of functional polystyrenes.

It is demonstrated that tetrahydrofuran (THF) should be used with caution as a solvent in polymer sample preparation for matrix-assisted laser desorption/ionization (MALDI) analyses. The presence of peroxides in THF may cause the oxidation of chemically active groups. This effect is illustrated in the case of S-containing polystyrene derivatives. The oxidation of the trithiocarbonate group resulted in the formation of poly(styrene)sulfonic acids, R(CH(2)CHPh)(n)SO(3)H, which was detected in negative mode by MALDI and electrospray ionization (ESI) methods after the samples remained in THF for several hours.

Furans↗

Quantitative equivalence between polymer nanocomposites and thin polymer films.

The thermomechanical responses of polymers, which provide limitations to their practical use, are favourably altered by the addition of trace amounts of a nanofiller. However, the resulting changes in polymer properties are poorly understood, primarily due to the non-uniform spatial distribution of nanoparticles. Here we show that the thermomechanical properties of 'polymer nanocomposites' are quantitatively equivalent to the well-documented case of planar polymer films. We quantify this equivalence by drawing a direct analogy between film thickness and an appropriate experimental interparticle spacing. We show that the changes in glass-transition temperature with decreasing interparticle spacing for two filler surface treatments are quantitatively equivalent to the corresponding thin-film data with a non-wetting and a wetting polymer-particle interface. Our results offer new insights into the role of confinement on the glass transition, and we conclude that the mere presence of regions of modified mobility in the vicinity of the particle surfaces, that is, a simple two-layer model, is insufficient to explain our results. Rather, we conjecture that the glass-transition process requires that the interphase regions surrounding different particles interact.

Elasticity↗