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A. J. Pennings

University of Groningen

Publishes on Polymer crystallization and properties, biodegradable polymer synthesis and properties, Polymer Nanocomposites and Properties. 127 papers and 9.5k citations.

127Publications
9.5kTotal Citations

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Crystal structure, conformation and morphology of solution-spun poly(L-lactide) fibers
W. Hoogsteen, A. R. Postema, A. J. Pennings et al.|Macromolecules|1990
Cited by 851

ABSTRACT: Depending on the spinning and drawing conditions, two crystal structures for solution-spun poly(L-lactide) are obtained. The pseudoorthorhombic a structure (a = 10.6, b = 6.1, and c = 28.8 A) contains two chains in the unit cell and is found at relatively low drawing temperatures and/or low hot-draw ratios. At higher drawing temperatures and/or higher hot-draw ratios a second so-called 0 structure appears. For this structure an orthorhombic unit cell is proposed (a = 10.31, b = 18.21, and c = 9.00 A) containing six chains. The chain conformations of the a and p structure are left-handed 10/3 and 3/1 helices, respectively. Calculations show that both conformations have approximately the same energy. Therefore, the preference for one of the two structures is determined by packing considerations. In fibers containing a mixture of CY and 0 structure, the latter seems to bear most of the load during stress-strain experiments. Meridional small-angle X-ray scattering experiments yield a maximum for fibers containing only a structure pointing to a lamellar folded-chain morphology. The (3 structure on the other hand seems to correspond to a fibrillar morphology. Differential scanning calorimetry on unconstrained fibers shows that the 0 structure melts at a lower temperature than the a structure. The large shift of the peak melting temperature to higher temperatures in melting experiments on constrained fibers indicates that both lamellae and fibrils contribute to the strength of the fibers. This points to a considerable amount of interconnections/ entanglements between adjacent lamellae. 1.

Lewis acid catalyzed polymerization of L-lactide. Kinetics and mechanism of the bulk polymerization
Cited by 401

The kinetics of the L-lactide bulk polymerization was studied using tin(II) bis(2-ethylhexanoate) and zinc bis(2,2-dimethyl-3,5-heptanedionato-O,O'). Up to 80% conversion, the rate of polymerization using tin(II) bis(2-ethylhexanoate) is higher than that with the zinc-containing catalyst, while at conversions beyond 80%, the latter catalyst has the higher rate of polymerization. Crystallization of the newly formed polymer has an accelerating effect on the polymerization. The difference in the rate of polymerization at high conversions for the two catalysts is caused by a difference in crystallinity of the newly formed polymer. Contaminants in the catalyst and monomer are the true initiators in these L-lactide polymerizations. Initiation as well as polymerization proceeds through a Lewis acid catalyzed transesterification reaction between an activated lactone and a hydroxyl group.