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Rate mechanisms of a novel thiol-ene photopolymerization reaction
Authors:Sirish K Reddy  Neil B Cramer  Allison K O' Brien  Tsali Cross  Rishi Raj  Christopher N Bowman
Institution:1. Department of Chemical and Biological Engineering, University of Colorado, Boulder, CO 80309-0424, USA, Fax: +1 303-492-3247, 303-492-4341;2. Department of Mechanical Engineering, University of Colorado, Boulder, CO 80309, USA
Abstract:A novel thiol-ene photopolymerization reaction involving copolymerization of tetrathiol monomer with vinyl silazane is experimentally characterized and is modeled successfully. The overall polymerization rate is found to be controlled by the ratio of the propagation to chain transfer kinetic parameters. The polymerization rate of this mixture, in the presence of added photoinitiator, is approximately first order in ene functionality and is independent of thiol functional group concentration. Initiation rates in this system, when cured utilizing a light centered around 365 nm light, and in the presence of no added photoinitiator, are shown to be proportional to the ene monomer concentration. When the mixture is polymerized utilizing light centered at 254 nm light, and without photoinitiator, the initiation rates are proportional to the thiol monomer concentrations. This novel reaction scheme is further utilized to form ultra rapidly polymerizable polymer derived ceramic structures with high aspect ratios.
Keywords:ceramics  crosslinking  initiatorless  modeling  thiol-ene
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