The creep behavior of an amorphous poly(etherimide) polymer is investigated in the vicinity of its glass transition in a weakly non linear regime where the acceleration of the creep response is driven by local configurational rearrangements. From the time shifts of the creep compliance curves under stresses from 1 to 15 MPa and in the temperature range between and , where is the glass transition temperature, we determine a macroscopic acceleration factor. The macroscopic acceleration is shown to vary as temperature with , where is the macroscopic stress and Y is a decreasing function of compliance. Because at the beginning of creep, the stress is homogeneous, the macroscopic acceleration is thus similar to the local one, in agreement with the recent theory of Long et al. (Phys Rev Mat 2:105601, 2018) which predicts . For larger compliances, the decrease of Y is interpreted as a signature of the development of stress disorder during creep.
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http://dx.doi.org/10.1140/epje/s10189-024-00468-x | DOI Listing |
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