Noy Bassik1, Beza Abebe2, and David H. Gracias1. (1) Department of Chemical and Biomolecular Engineering, Johns Hopkins University, 125 Maryland Hall, 3400 N Charles Street, Baltimore, MD 21218, (2) Department of Materials Science, Johns Hopkins University, Baltimore, MD
We investigated the solvent driven motion of lithographically structured poly-N-isopropylacrylamide (PNIPAm) gels. The gels were soaked in ethanol and then transferred to water, where they moved spontaneously. This movement was driven by the expulsion of the ethanol from the gel and subsequent ethanol spreading at the air-water interface. We utilized lithographic patterning of the gels at the micron-millimeter length scales to investigate the effect of size, shape and symmetry. Gels were lithographically patterned with features less than 100 microns, and exhibited remarkably high linear and rotational velocities of up to 31 cm/sec and 3529 rpm over time spans of seconds to minutes. We observed a reciprocal dependence of maximum rotational velocity on linear dimension. The linear velocity for all types of motion, along a line or curve, was analyzed and found to be similar across different shapes and sizes. This velocity was in the range of 17-39 cm/sec even though our sizes and shapes varied across orders of magnitude. We believe this velocity is related to the velocity of spreading of ethanol on water, which is approximately 53 cm/sec. Additionally, since this solvent powered motion is a clean, quiet and reusable source of motive power, with no need for on-board wiring or batteries, we explored applications in moving lithographically integrated metallic payloads on top of the gels and utilized the gels to move larger floating objects.