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Silk fibroin (SF), a unique and promising natural material extracted from silkworm, has gained much attention for its use as biomedical material, because of its biocompatibility, biodegradability, and nontoxicity. Despite its strength, SF alone is not appropriate because of its poor flexibility. Thermoplastic polyurethane (TPU) is a very desirable material for medical applications because of its flexibility. A solution to the problem of SF’s poor flexibility can be achieved by mixing flexible TPU with SF. The aim of this work was to examine the influence of FS content on the physical and thermal properties of TPU/FS blends. Blends of SF and TPU were prepared with melt mixing of TPU with 5, 10, 15, and 20 wt% of SF in a laboratory Brabender kneading chamber. The specimens of the neat components and their blends were moulded in a hydraulic press. The structural characteristics, thermal, and viscoelastic properties of neat TPU, SF and their blends (TPU/SF blends) were examined by Fourier transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and thermogravimetric analysis (TGA). The FTIR results showed that the SF was successfully introduced to TPU matrix. Results obtained with DSC and DMA measurements showed that, when the SF content increased in the TPU/SF blends, the Tg, expressed as Teig, Tmg, and Tefg of the TPU, slightly shifted to lower temperature due to the incorporation of the amorphous phase of FS (aspartic acid) in the amorphous phase of TPU, and mobility of polymer chains increased. The melting temperature (Tm), expressed as Teim, Tpm, and Tefm, decreased because of the less organised crystal structure with the addition of SF. Thermal stability was determined by TGA, which showed that, with the addition of SF, the thermal stability decreased because of the lower thermal stability of SF. [ABSTRACT FROM AUTHOR]

In this work, the influence of multiwalled carbon nanotubes (MWCNT) and carbon nanotubes modified with COOH groups (MWCNT-COOH) on the structure and properties of thermoplastic polyurethane (PU) were investigated. The samples of nanocomposite were prepared from a mixture of polyurethane and MWCNT in acetone by slow drying at room temperature. The effect of the addition of nanofillers on the spherulite structure of polyurethane and the distribution of the nanofillers in the PU matrix were analysed with optical polarization microscopy. Thermal properties in non-isothermal and isothermal conditions were investigated by differential scanning calorimetry (DSC). The results of contact angle measurement imply that modification of MWCNT surface with COOH groups changes its surface from hydrophobic to hydrophilic (Fig. 2 and Table 1). Optical polarization microscopy showed that the addition of both nanofillers disrupts the coarse spherulite morphology of the polyurethane matrix (Fig. 4 and Fig. 5). It was observed that, at the macro level, the modified MWCNT-COOH filler is better distributed in the PU matrix than is the MWCNT filler (Fig. 5). The DSC results showed that, in non-isothermal conditions, up to a certain amount, both nanofillers accelerate the crystallization of the soft segments of polyurethane. This effect is more pronounced in systems with MWCNT filler (Fig. 9). The results of the crystallization enthalpy during cooling showed that MWCNT filler, despite its worse distribution in the PU matrix, more significantly enhances crystallization of PU’s soft segment than does the MWCNT-COOH filler (Fig. 10). This conclusion can be ascribed to better compatibility between the nonpolar MWCNT filler and the nonpolar soft phase of the PU matrix, as well as to the previous scientific finding that functional groups at MWCNT surface decrease the nucleation effect of MWCNT. By analysing the melting peaks, it can be concluded that the PU systems with MWCNT compared to systems with MWCNT-COOH contain a higher proportion of less ordered crystalline soft phase (Fig. 11). In isothermal conditions, the MWCNT filler accelerates crystallization more significantly than does the MWCNT-COOH filler (Fig. 16). [ABSTRACT FROM AUTHOR]

The widespread use of thermal analysis (TA) by scientists as a laboratory technique carries with it a working vocabulary. This document is intended to provide those working in the field with a consistent set of definitions to permit clear and precise communication as well as understanding. Included in the document are the definitions of 13 techniques, 54 terms within the glossary, as well as symbols and units. [ABSTRACT FROM AUTHOR]

The document gives definitions of terms met in the conventional thermal and thermomechanical characterisation of polymeric materials. [ABSTRACT FROM AUTHOR]

The infl uence of repeated extrusions of polypropylene (PP) on its thermal properties is investigated by differential scanning calorimetry and non-isothermal thermogravimetric analysis. PP is extruded six times on a laboratory extruder at a temperature of 190 °C and screw speed of 120 min-1. Extruded samples show a slight reduction of the melting point and the crystallization degree compared to the original PP. The non-isothermal degradation of all samples occurs through one degradation step and the extruded samples show a slightly lower thermal stability compared to the original PP. Kinetics analysis of the non-isothermal degradation of all samples was performed by isoconversional Flynn-Wall-Ozawa method. All extruded samples show higher values of activation energy compared to the original PP. Activation energy is constant in a wide range of conversion for all samples what also indicates that the non-isothermal degradation of PP occurs through one degradation step, without change of the reaction mechanism due to extrusion. Therefore, repeated extrusions under these conditions slightly worsen the thermal properties of PP and can be used for recycling its waste. [ABSTRACT FROM AUTHOR]