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Abstracts - Conference Planning and Management - Iowa State ...

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Results<br />

The activation strain, activation stress <strong>and</strong> activation strain energy were higher at higher shear rates <strong>and</strong><br />

were linearly dependent on shear rate. In an effort to lower the activation parameters, the major crosslinker<br />

(EGDMA) was replaced with PEG-550. We hypothesized that the longer length of the PEG<br />

chains compared to the spiropyran molecule would enhance load transfer to the spiropyran, thus<br />

leading to mechanical activation at a lower bulk shear stress <strong>and</strong> strain. The result of changing the<br />

major cross-linker from EGDMA to PEG was a lower activation shear strain, shear stress <strong>and</strong> strain<br />

energy for all shear rates. A summary of activation parameters is given in Table 1. Control tests were<br />

performed on PMMA with monofunctional spiropyran [2] <strong>and</strong> PMMA with no spiropyran. As expected,<br />

no color change resulted from the shear testing. (Figure 1) Experiments are in progress to underst<strong>and</strong><br />

the role of crosslink length, crosslink density, <strong>and</strong> the incorporation of other mechanophores on the<br />

shear-induced chemical reactions.<br />

Figure 1: Images of active <strong>and</strong> control samples cross-linked with EGDMA before <strong>and</strong> after testing at each<br />

shear rate.<br />

Table 1: Strain, stress <strong>and</strong> strain energy levels at activation for both EGDMA <strong>and</strong> PEG cross-linked<br />

polymers at each shear rate.<br />

[1] Potisek, S.L., Davis, D.A., Sottos, N.R., White, N.R., White, S.R., Moore, J.S. 2007,<br />

Mechanophore-Linked Addition Polymers. J. Am. Chem. Soc. 129, 13808-13809.<br />

[2] Davis, D.A., Hamilton, A., Yang, Y. Cremar, L.D., Gough, D.V., Potisek, S.L., Ong, M.T. Braun,<br />

P.V., Martínez, T.J., White, S.R., Moore, J.S., Sottos, N.R. 2009, Force-Induced Activation of<br />

Covalent Bonds in Mechanoresponsive Polymers. Nature. 459, 68-72.<br />

Society of Engineering Science ▪ 47 th Annual Technical Meeting 24

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