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Lifetime predictions for semi-crystalline cable insulation materials: I. Mechanical properties and oxygen consumption measurements on EPR materials

Long-term accelerated aging studies (up to 7 years of aging) were conducted on four typical EPR materials used as cable insulation in nuclear power plant safety applications with the goal of establishing lifetime estimates at typical aging conditions of ∼50 °C. The four materials showed slow to mode...

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Bibliographic Details
Published in:Polymer degradation and stability 2006-09, Vol.91 (9), p.2146-2156
Main Authors: Gillen, K.T., Bernstein, R., Clough, R.L., Celina, M.
Format: Article
Language:English
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Summary:Long-term accelerated aging studies (up to 7 years of aging) were conducted on four typical EPR materials used as cable insulation in nuclear power plant safety applications with the goal of establishing lifetime estimates at typical aging conditions of ∼50 °C. The four materials showed slow to moderate changes in mechanical properties (tensile elongation) until just before failure where abrupt changes occurred (so-called “induction-time” behavior). Time–temperature superposition was applied to derive shift factors and probe for Arrhenius behavior. Three of the materials showed reasonable time–temperature superposition with the empirically derived shift factors yielding an approximate Arrhenius dependence on temperature. Since the elongation results for the fourth material could not be successfully superposed, consistency with Arrhenius assumptions was impossible. For this material the early part of the mechanical degradation appeared to have an Arrhenius activation energy E a of ∼100 kJ/mol (24 kcal/mol) whereas the post-induction degradation data had an E a of ∼128 kJ/mol. Oxygen consumption measurements were used to confirm the 100 kJ/mol E a found from early-time elongation results and to show that the chemistry responsible before the induction time is likely to remain unchanged down to 50 °C. Reasonable extrapolations of the induction-time results indicated 50 °C lifetimes exceeding 300 years for all four materials.
ISSN:0141-3910
1873-2321
DOI:10.1016/j.polymdegradstab.2006.01.009