Peculiarities of supermolecular structure of polyimides and polyester imides

Abstract

Supermolecular structures of fourteen heterocyclic thermally stable polymers of the polyimide (PI) and polyesterimide (PEI) class have been investigated by X‐ray scattering, optical, dilatometric and thermomechanical methods. Quasi‐crystalline structure of these polymers in the initial amorphous state of poly(amic acid) and poly(ester amic acid) and also after chemical imidization has been revealed. The quasi‐crystalline structure is characterized by a biaxial polarizability ellipsoid with a negative sign. This is indicated by distinct conoscopic figures recorded with a polarizing microscope. The effect of the number of oxyphenylene groups on the crystallizability of PI and PEI was investigated. For PEI the effect of self‐orientation of macromolecules induced by conformational transition was observed. Discrete small‐angle x‐ray scattering pattern (a long period) was also revealed for PEI. The appearance of long periods is caused by polymorphism of PEI uniquely determined for one of its types (PEI‐II). X‐ray scattering data confirmed by calculations of the lattice energy show that dianhydride pyromellitimide chain portion is the element determining the crystalline structure of PI. The structure is determined by van der Waals' forces and obeys the principle of dense packing. This leads to the appearance of layer structure with alternating layers of diamine and dianhydride portions. It was found that, depending on the rigidity of the diamine portion, PI and PEI exhibit different abilities of forming axial‐planar or axial textures in nonoriented films.