Controlled Polymer Nanostructures through Photopolymerization Kinetics and Moleuclar Self-assembly

Student: Brad Forney

Control of matter on the atomic scale has greatly increased the performance of many useful products including microprocessors, electronic displays, and semiconductors to name a few.  The improved performance of these products originates from material properties dependent on submicron order.  Polymers with nanometer size structures are generating significant research interest due to their potential application in areas including tissue engineering, controlled release, catalysis, and size-selective separation media.  The periodic nanostructures of these polymers can greatly improve properties useful in many advanced biological and industrial applications.  Our research utilizes photopolymerization kinetics and self-assembling lyotropic liquid crystals (LLCs) to direct polymer structure on the nanometer scale (Figure 1).  The goal is to control polymer nanostructure by optimizing the polymerization speed and environment in which polymerization occurs in order to optimize material properties dependent on submicron order. 

Figure 1:  Diagram showing the process used to synthesize nanostructured polymers from self-assembled LLC templates.  Clockwise from bottom left: hexagonal and lamellar LLC structures with nanometer scale dimensions, cross-section of the hexagonal LLC structure, hexagonal LLC structure dispersed with two monomers, and photopolymerized monomers with hexagonal nanostructure after the LLC template is removed.      

 



































Chemical and Biochemical Engineering
4133 Seamans Center for the Engineering Arts and Sciences
Iowa City, Iowa 52242-1527 USA
Tel: 319.335.1400
Fax: 319.335.1415
mailto:chemeng@engineering.uiowa.edu