Structural Evolution of Hard-Elastic Isotactic Polypropylene Film during Uniaxial Tensile Deformation: The Effect of Temperature
2018
Lin, Yuanfei | Li, Xueyu | Meng, Lingpu | Chen, Xiaowei | Lv, Fei | Zhang, Qianlei | Zhang, Rui | Li, Liangbin
The effects of temperature on the nonlinear mechanical behaviors of hard-elastic isotactic polypropylene films are systematically studied with in-situ ultrafast synchrotron radiation small- and wide-angle X-ray scattering techniques (SAXS/WAXS) during uniaxial tensile deformation at temperatures from 30 to 160 °C. Based on the mechanical behaviors and structural evolutions in strain–temperature two-dimensional space, three temperature regions (I, II, and III) are clearly defined with the α relaxation temperature (Tα ≈ 80 °C) and the onset of melting temperature (Tₒₙₛₑₜ ≈ 135 °C) as boundaries, where different mechanisms dominate the nonlinear deformations after yield. In region I, microstrain in lamellar stacks εₘ obtains an accelerated increase after yield and reaches a value significantly larger than corresponding macrostrain ε, during which neither slipping, melting, nor cavitation occurs. We propose stress-induced microphase separation of interlamellar amorphous to be responsible to the hyperelastic behavior in region I. Above Tα in region II, due to reduced cohesive strength and enhanced chain mobility, the irreversible reduction of crystallinity and the formation of slender cavities suggest that crystal slipping overwhelms microphase separation and plays the major role in nonlinear deformation, during which chains in lamellar crystals are pulled out and recrystallize into nanofibrillar bridges. In region III above Tₒₙₛₑₜ, melting–recrystallization dictates the nonlinear deformation. A schematic roadmap for structural evolution is constructed in strain–temperature space, which may guide the processing of microporous membranes for lithium battery separators as well as other high performance polymer fibers and films.
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