On the structure of glassy polymers. III. Small‐angle x‐ray scattering from amorphous polyethylene terephthalate

Abstract

The small‐angle x‐ray scattering (SAXS) from glassy polyethylene terephthalate has been measured using a Bonse–Hart system. The data cover the angular range (2θ) between 20 sec and 2 deg. After correcting for absorption, background, and beam divergence, the data have been placed on an absolute basis by comparison with the scattering from a standard silica suspension. The corrected absolute intensity decreases strongly with increasing angle over the range between 20 sec and 15 min, decreases more gradually in the range between 15 min and 45 min, and reaches a nearly constant asymptotic value over the range between 45 min and 2 deg. The magnitude of the scattering in the constant range, about 0.4 (electrons)² Å⁻³, is very close to the value predicted by the thermodynamic fluctuation theory for fluids applied at the glass‐transition temperature [0.34 (electrons)² Å⁻³]. The increase in intensity at angles smaller than about 45 min cannot be described by structures on the scale and volume fraction of the nodules reported in amorphous PET (50–100 Å), but can be well represented by small concentrations of heterogeneities, ranging in size from 100 to 2000 Angstroms, superimposed on the thermal density fluctuations frozen‐in at the glass transition. The bulk structure of this material seems well described as a random amorphous solid, containing simple thermal fluctuations and a small concentration (<1 vol‐%) of heterogeneities covering a range of sizes. The heterogeneities in the small end of the range may well be crystallites which formed on cooling.