Abstract
Using the high-resolution ion profiling techniques of secondary ion mass spectrometry (SIMS) and time of flight forward recoil elastic scattering (TOF-FRES), we have measured the surface concentration profiles for a series of deuterated polystyrene (d-PS)/hydrogenated polystyrene (h-PS) blends as a function of deuterium volume fraction and annealing time. The data show that the profile is formed at a rate determined mostly by the bulk mutual diffusion coefficient. The form of the profile away from the surface (Z > 100 Å) is in agreement with predictions of current mean-field theories. On the other hand, in the near surface region (Z < 100 Å) a distinct flattening of the profile is observed, indicating that the short-ranged form of the interaction assumed in these theories may not be valid.
| Original language | English |
|---|---|
| Pages (from-to) | 5991-5996 |
| Number of pages | 6 |
| Journal | Macromolecules |
| Volume | 24 |
| Issue number | 22 |
| DOIs | |
| State | Published - Oct 1 1991 |
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