Nanostructure and mechanical properties studied during dynamical straining of microfibrillar reinforced HDPE/PA blends

Oriented polymer blends whose major component is high‐density polyethylene (HDPE) are strained until failure. Two‐dimensional (2D) small‐angle X‐ray scattering (SAXS) patterns monitor the nanostructure evolution, which is related to the macroscopic mechanical evolution. Data evaluation methods for high‐precision determination of macroscopic and nanoscopic parameters are presented. The hardest materials exhibit a very inhomogeneous nanodomain structure. During straining, their domains appear to be wedged and inhibit transverse contraction on the nanometer scale. Further components of the blends are polyamide 6 (PA6) or polyamide 12 (PA12) (20–30%) and Yparex® 8102 (YP) as compatibilizer (0–10%). Some HDPE/PA6 blends are additionally loaded with commercial nanoclays (Nanomer® or Cloisite®), the respective amounts being 7.5% and 5% with respect to PA. Blending of HDPE with PA12 causes no synergistic effect. In the absence of nanoclay, PA6 and HDPE form a heterogeneous nanostructure with high macroscopic Young's modulus. After addition of YP a rather homogeneous scaffold structure is observed in which some of the PA6 microfibrils and HDPE crystallites appear to be rigidly connected, but the modulus has decreased. Both kinds of nanoclay induce a transition in the HDPE/PA6 blends from a structure without transverse correlation among the microfibrils into a macrolattice with 3D correlations among the HDPE domains from neighboring microfibrils. In the range of extensions between 0.7 and 3.5%, the scattering entities with 3D correlation show transverse elongation instead of transverse contraction. The process is interpreted as overcoming a correlation barrier executed by the crystallites in an evasion‐upon‐approaching mechanism. During continued straining, the 3D correlation is reduced or completely removed. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 237–250, 2010     

Synthesis,characterization, and cross‐linking of a library of statistical copolymers based on 2‐“soy alkyl”‐2‐oxazoline and 2‐ethyl‐2‐oxazoline

The synthesis of statistical copolymers consisting of 2‐ethyl‐2‐oxazoline (EtOx) and 2‐“soy alkyl”‐2‐oxazoline (SoyOx) via a microwave‐assisted cationic ring‐opening polymerization procedure is described. The majority of the resulting copolymers revealed polydispersity indices below 1.30. The reactivity ratios (r_EtOx 1.4 ± 0.3; r_SoyOx = 1.7 ± 0.3) revealed a clustered monomer distribution throughout the polymer chains. The thermal and surface properties of the pEtOx‐stat‐SoyOx copolymers were analyzed before and after UV‐curing demonstrating the decreased chain mobility after cross‐linking. In addition, the cross‐linked materials showed shape‐persistent swelling upon absorption of water from the air, whereby as little as 5 mol % SoyOx was found to provide efficient cross‐linking. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5371,–5379, 2007     

Allgemeine Anzahlfunctionen für Kegelschnitte,Flächen und Räume zweiten Grades inn Dimensionen

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