Josef Baldrián

Abstract The commercial grade of isotactic polypropylene was modified by a specific β‐nucleating agent in a broad concentration range. The supermolecular structure of the specimens prepared by injection molding was characterized by X‐ray scattering and correlated with mechanical behavior. It was found that at a critical nucleant concentration of 0.03 wt % the content of the β‐modification virtually reaches a saturation level. With further addition of the nucleant, the β‐phase content increases only slightly. The long period passes through a distinct maximum at the same nucleant concentration. This singularity in structure remarkably correlates with a minimum of the yield stress and maxima of strain at break and fracture toughness. Such general behavior is also reflected in the correlation between the β‐phase concentration and fracture toughness profiles along the injection‐molded bars. It is suggested that in the critically nucleated material an optimum thickness of the amorphous interlayer with connecting chains between the β‐crystallites is established, rendering the material the highest possible ductility and toughness. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1174–1184, 2002

Ultra-high molecular weight polyethylene (UHMWPE) was irradiated with accelerated electrons (1 MeV in air) using high dose rates (> 25 kGy/min) and thin specimens (thickness 1 mm). Parts of the specimens were remelted (200 degrees C for 10 min; 150 degrees C for 0, 2, 10, 30, 60 min). All specimens were stored in nitrogen in the dark at 5 degrees C. Supermolecular structure, extent of crosslinking, oxidative degradation, and macroradical content were studied by a number of methods (SAXS, WAXS, SEM, DSC, FTIR, ESR, TGA, solubility experiments, image analysis). The results obtained with irradiated samples were compared with those obtained with irradiated and remelted samples. It was confirmed that crosslinking predominates over chain scission at very high dose rates, even if the irradiation is performed in air. Discrepancies concerning supermolecular structure changes in UHMWPE after irradiation and thermal treatment, found in various studies in the literature, are discussed. A simple model, which describes and explains all supermolecular structure changes, is introduced. An effective way of eliminating residual macroradicals in UHMWPE is proposed.

Ordered structures in samples of Bisphenol A polycarbonate (BPAPC) prepared by varying thermal and solvent conditions were investigated by infrared and Raman spectroscopy, wide-angle X-ray scattering (WAXS), and differential scanning calorimetry (DSC). Based on the spectroscopic analysis and ab initio quantum mechanical calculations of diphenyl carbonate as a model compound, an assignment of the bands conformationally sensitive to the trans−trans and cis−trans structures is proposed. Temperature dependences of the vibrational spectra of BPAPC show that cis−trans structure is the energetically preferred conformation in the amorphous state and in solution and its population can be increased with decreasing temperature in amorphous BPAPC even below the glass transition temperature. Differences in the degrees of ordering in semicrystalline BPAPC assessed from the vibrational spectra, WAXS, and DSC indicate partial order in the interfacial region between the crystalline and amorphous phases. In some solvents (toluene, benzene), aggregation of BPAPC occurs, leading to the ordered structure analogous to crystalline BPAPC. The order is preserved in semicrystalline BPAPC obtained by the room-temperature evaporation of the solvent.