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FUNCTIONAL POLYMER LABORATORY

 

JUST PUBLISHED - SOME OF OUR MOST RECENT RESEARCH HIGHLIGHTS

March 2008: Capadona, J.R; Shanmuganathan K.; Tyler, D.; Rowan, S.J.; Weder, C.; Bio-inspired chemo-mechanical polymer nanocomposites that mimic the sea cucumber dermis; Science 2008, 319, 1370-1374.

The paper published in one of the world’s most prestigious scholarly scientific journals reports ground-breaking work on a new type of polymer that displays mechanic adaptability. Using the skin of sea cucumbers as blueprint, we developed new polymer nanocomposites, which can change their mechanical properties on command. The new materials were designed to respond to a chemical stimulus – exposure to water – and are comprised of a low modulus polymer matrix into which strong and rigid nanofibers are embedded so that they form a network. In the absence of water, the nanofibers are ‘glued’ to each other and the nanofiber network dominates the mechanical properties of the material. In this state, the material is strong and rigid. If the material is exposed to water, it swells very slightly. The water molecules ‘unglue’ the nanofibers and the material becomes about 1000 times softer. Its properties now resemble those of a rubber. The new materials may be useful for a range of applications. Our current focus is the development of “smart” cortical implants. Microelectrodes based on the new polymers are stiff when implanted, but then turn flexible. This adaptability may have significant clinical advantages. The project is a collaboration with the groups of Profs. Stuart Rowan, Dustin Tyler, and Dr. Jeff Capadona is part of the Advanced Platform Technology (APT) Center at the Louis Stokes Cleveland VA Medical Center,

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February 2008: Kunzelman, J.; Chung, C.; Mather, T.M.; Weder, C.; Shape Memory Polymers with Built-In Threshold Temperature Sensors; J. Mater. Chem. 2008, 18, 1082 - 1086.

New shape memory polymers with built-in temperature sensors were developed by integrating excimer-forming fluorescent chromophores into a cross-linked poly(cyclooctene) matrix. Color changes resulting from self-assembly or dispersion of dye molecules allow one to monitor reaching of the set/release temperature of the materials. The work, a collaboration with Prof. Pat Mather’s group at Syracuse University, was selected for the back cover of the journal and highlighted as a hot paper. A US patent that broadly covers this technology has been issued to Case Western Reserve University.

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December 2007: Capadona, J.R; van den Berg, O.; Capadona, L.; Tyler, D.; Rowan, S.J.; Weder, C.; A versatile approach for the processing of polymer nanocomposites with selfassembled nanofibre templates; Nature Nanotechnology 2007, 2, 765-769.

The incorporation of nanoparticles into polymers is a design approach that is employed in all areas of materials science. The concept is attractive since it enables the creation of materials with new or improved properties by mixing multiple constituents and exploiting synergistic effects. The broad technological exploitation of polymer nanocomposites is, however, stifled by the lack of effective methods to control nanoparticle dispersion. Our latest paper reports a simple and versatile process for the formation of homogeneous polymer/nanofiber composites. The approach is based on the formation of a three-dimensional template of well-individualized nanofibers, which is filled with any polymer of choice. We demonstrate that this template approach is broadly applicable and allows for the fabrication of otherwise inaccessible nanocomposites of immiscible components.

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December 2007: Weder, C.; Hole Control in Microporous Polymers; Angew. Chem. Int. Ed. 2007 Invited Highlight, Early View (DOI 10.1002/anie.200704697).

Microporous materials with large specific surface area and pore sizes of molecular dimensions are of interest due to their use in applications that range from selective membranes to molecular sieves to catalysts to photonic crystals. Organic polymers would represent a desirable alternative to inorganic porous materials, since they combine low density with good mechanical properties and ease of processing. However, until recently it was impossible to gain control over their porosity, especially the pore sizes. Several approaches have emerged to solve this problem. Chris Weder’s article in Angewandte Chemie highlights work by Andy Cooper et al., who reported that control over pore size can be achieved in amorphous conjugated poly(arylene ethynylene) networks.

   

October 2007: Islangulov, R.R.; Lott, J.; Weder, C.; Castellano, F.N.; Noncoherent Low-Power Upconversion in Solid Polymer Films; J. Am. Chem. Soc. 2007, 129, 12652-12653.

Noncoherent low-power photon upconversion has been realized in solid thin films composed of an ethyleneoxide/epichlorohydrin copolymer doped with palladium octaethylporphyrin (PdOEP) and 9,10-diphenylanthracene (DPA). Selective excitation of PdOEP at 544 nm generates easily visualized DPA fluorescence in the blue with noncoherent light sources under ambient laboratory conditions.  The work, published in the Journal of the American Chemical Society, is a collaboration with Felix N. Castellano's group at Bowling Green State University.

  

August 2007: Kunzelman, J.; Crenshaw, B.R.; Weder, C.; Self-Assembly of Chromogenic Dyes - A New Mechanism for Humidity Sensors; J. Mater. Chem. 2007, 17, 2989-2991.

Upon self-assembly, certain photoluminescent chromophores exhibit pronounced changes of their optical absorption properties. The integration of these dyes into a polymer matrix allows facile monitoring of external stimuli, for example mechanical stress, temperature history, or - as shown in this new paper published in the Journal of Materials Chemistry - exposure to moisture. The work was selected for the cover of the august issue of the journal. A US patent that broadly covers this technology has just been issued to Case Western Reserve University.

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