Block copolymers, long chain molecules of two distinct chemical species joined
covalently to one another, have long been known to form organized structures on the nanoscopic level. For example, if the two chains are the same length a lamellar structure results . In this work we show how this internal structure causes distinct deviation from 'normal' fluid behavior. We begin with the observation of block copolymer droplets with atomic force microscopy. We note the droplets form nearly conical shapes in stark contrast to the usual spherical cap. These droplets are found t o spread at an incredibly slow speed, and to have interesting instabilities in their wetting layer. We move on to studies of completely wet substrates (i.e. thin films) near the order-disorder transition of the material. Here we directly observe, with optical microscopy, a change in the fundamental spacing of the diblock's internal structure. This represents a superior method of measurement of the Flory-Huggins interaction parameter, which we verify in several ways. We also use the change in lamellar thickness to drive diffusion from one layer to another, and by similar measurements we can determine the kinetics of diffusion between the lamellar layers. In the last study we measure the lamellar edges on a gradient thickness sample with optical microscopy. In so doing we can directly observe surface induced ordering, and for the first time, can precisely resolve the near surface ordering dynamics. / Thesis / Doctor of Philosophy (PhD)
| Identifer | oai:union.ndltd.org:mcmaster.ca/oai:macsphere.mcmaster.ca:11375/16578 |
| Date | January 2008 |
| Creators | Croll, Andrew B. |
| Contributors | Dalnoki-Veress, K., Physics |
| Source Sets | McMaster University |
| Language | English |
| Detected Language | English |
| Type | Thesis |
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