Melt spinning of poly(3-hydroxybutyrate) for tissue engineering using electron-beam-irradiated poly(3-hydroxybutyrate) as nucleation agent.

Electron-beam-irradiated poly(3-hydroxybutyrate) was used as a nucleating agent for poly(3-hydroxybutyrate) in a melt-spinning process. Molecular data and thermal properties of the irradiated samples were determined. The thermal properties of the nucleated melts were determined to assess the influence of the nucleation agents, and then spinning tests were carried out. Thermal and textile properties of the spun fibers were also determined. Estimations of the improvement of the crystallization in the spinline and of the inhibition of secondary crystallization in the fibers from the use of the described blood-compatible nucleation agents are given.

Melt spinning of bacterial aliphatic polyester using reactive extrusion for improvement of crystallization.

This paper reports on an attempt to use reactive extrusion with peroxide as a comfortable pathway for improvement of the crystallization of poly(3-hydroxybutyrate) in a melt spinning process. At first, rheological and thermal properties of the modified melts are determined in order to assess the effect of nucleation. Then spinning tests are carried out. Molecular weights and molecular weight distributions of the spun fibers are determined by chromatographic methods. Average crystallite size is measured by wide angle X-ray scattering. Thermal and textile properties of the spun PHB fibers are also determined. An estimation of the improvement of the crystallization in the spinline and of the inhibition of the secondary crystallization in the fibers from the use of the described way of reactive extrusion is given.

Determination of low amounts of long-chain branches in polypropylene using a combination of chromatographic and rheological methods.

The focus of our investigations lies on the detection of low amounts of long-chain branching (LCB) in isotactic polypropylene (iPP) created by electron beam irradiation. The modified samples were investigated by rheological experiments in shear and elongational flow and by size-exclusion chromatography. The comparison of the results demonstrates the efficiency and the detection limits of these methods, particularly at very low degrees of long-chain branching. The combination of chromatographic and rheological methods enables a sensitive and comprehensive way for the characterisation of the long-chain branching phenomena.

Structure characterization of hyperbranched poly(ether amide)s. I. Preparative fractionation.

The focus of our investigation lies on the separation of typically broadly distributed hyperbranched poly(ether amide)s into narrow fractions of various molar masses. Their exact molar mass found via size-exclusion chromatography (SEC) with light uttering detection allows us to use these fractions for sample specific calibration in the SEC investigation of other hyperbranched samples. The analysis of the degree of branching, molar mass and viscosity behavior of the fractions gives a first indication about their molecular shape and the contribution of that shape to the overall viscosity. We determined the Mark-Houwink exponent for a hyperbranched sample using a number of narrow fractions which showed that an increase of molar mass leads to an increased molecular density.