Yin Huajie, Chua Yeong Zen, Yang Bin, Schick Christoph, Harrison Wayne J, Budd Peter M, Böhning Martin, Schönhals Andreas
Bundesanstalt für Materialforschung und-prüfung (BAM) , Unter den Eichen 87 , 12205 Berlin , Germany.
University of Rostock , Institute of Physics and Competence Center CALOR , Albert-Einstein-Str. 23-24 , 18059 Rostock , Germany.
J Phys Chem Lett. 2018 Apr 19;9(8):2003-2008. doi: 10.1021/acs.jpclett.8b00422. Epub 2018 Apr 6.
Polymers with intrinsic microporosity (PIMs) represent a novel, innovative class of materials with great potential in various applications from high-performance gas-separation membranes to electronic devices. Here, for the first time, for PIM-1, as the archetypal PIM, fast scanning calorimetry provides definitive evidence of a glass transition ( T = 715 K, heating rate 3 × 10 K/s) by decoupling the time scales responsible for glass transition and decomposition. Because the rigid molecular structure of PIM-1 prevents any conformational changes, small-scale bend and flex fluctuations must be considered the origin of its glass transition. This result has strong implications for the fundamental understanding of the glass transition and for the physical aging of PIMs and other complex polymers, both topical problems of materials science.
具有固有微孔性的聚合物(PIMs)是一类新型的创新材料,在从高性能气体分离膜到电子设备等各种应用中具有巨大潜力。在此,首次对作为典型PIM的PIM-1而言,快速扫描量热法通过解耦负责玻璃化转变和分解的时间尺度,提供了玻璃化转变(T = 715 K,加热速率3×10 K/s)的确切证据。由于PIM-1的刚性分子结构阻止了任何构象变化,小规模的弯曲和挠曲波动必须被视为其玻璃化转变的起源。这一结果对于深入理解玻璃化转变以及PIMs和其他复杂聚合物的物理老化具有重要意义,而这两者都是材料科学中的热门问题。