Derrick Stevens

Fabrication and characterization of electrospun chitosan nanofibers formed via templating with polyethylene oxide.

Chitosan is an abundantly common, naturally occurring, polysaccharide biopolymer. Its biocompatible, biodegradable, and antimicrobial properties have led to significant research toward biological applications such as drug delivery, artificial tissue scaffolds for functional tissue engineering, and wound-healing dressings. For applications such as tissue scaffolding, formation of highly porous mats of nanometer-sized fibers, such as those fabricated via electrospinning, may be quite important. Previously, strong acidic solvents and blending with synthetic polymers have been used to achieve electrospun nanofibers containing chitosan. As an alternative approach, in this work, polyethylene oxide (PEO) has been used as a template to fabricate chitosan nanofibers by electrospinning in a core-sheath geometry, with the PEO sheath serving as a template for the chitosan core. Solutions of 3 wt % chitosan (in acetic acid) and 4 wt % PEO (in water) were found to have matching rheological properties that enabled efficient core-sheath fiber formation. After removing the PEO sheath by washing with deionized water, chitosan nanofibers were obtained. Electron microscopy confirmed nanofibers of approximately 250 nm diameter with a clear core-sheath geometry before sheath removal, and chitosan nanofibers of approximately 100 nm diameter after washing. The resultant fibers were characterized with IR spectroscopy and X-ray diffraction, and the mechanical and electrical properties were evaluated.

Dynamics within Alkylsiloxane Self-Assembled Monolayers Studied by Sensitive Dielectric Spectroscopy

Self-assembled monolayers are a ubiquitous laboratory tool and have been the subject of many experimental investigations which have primarily focused on static properties of full coverage monolayers, with the maximum density and ordering possible. In this work, dynamics within low density, planar siloxane self-assembled monolayers are studied utilizing highly sensitive dielectric spectroscopy. Dilute, disordered films were intentionally fabricated in order to study the widest range of possible motions. At low coverage, an interacting relaxation is observed, which has similar dynamics to polyethylene-like glass transitions observed in phase-segregated side-chain polymers, despite the rigidity of the substrate and the constraint of ethyl groups in relatively short chains. As density is increased, a second local relaxation, previously observed in three-dimensional SAMs and associated with rotation within a small segment of the alkyl chain, is also observed.