材料科学
复合材料
热成型
造型(装饰)
压缩成型
玻璃化转变
聚合物
极限抗拉强度
聚酰亚胺
背景(考古学)
成形性
模具
图层(电子)
生物
古生物学
作者
Changxin Wan,Dan Jia,Shengpeng Zhan,Wulin Zhang,Tian Yang,Yinhua Li,Jian Li,Haitao Duan
标识
DOI:10.1177/09540083221148392
摘要
A compacted body was fabricated by pulverulent polyimide (PI) block copolymers using solid-like state compression molding (SCM) technique. Polymer heated to solid-like state, i.e. the high-elastic non-melting state above the glass transition temperature ( T g ) and well below melting temperature, could achieve plasticity due to dramatic decreases in elastic modulus. Tensile properties were taken as response values, and the results of single-factor experiments indicated that molding temperature was the dominant parameter on mechanical performances, followed by molding pressure and holding time. Within this context, the SCM process possesses a longer processing time window whereas the processing temperature is narrow. The manufacturing defects induced by inappropriate processing conditions also hurt the tribological performance of PIs. Particles in a solid-like state could coalesce tightly only by exerting both high temperature and pressure in the SCM process. Thermoforming mechanism examined by atomic-scale molecular dynamics simulation indicated that non-bonding interaction forces, especially van der Waals forces play a key role in fusing among polymeric particles. This study is devoted to establishing the interdependence of structure-formability-property for high-temperature polymers that are not melt processible.
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