Photoinduced-absorption investigation of oriented polymer systems: Polyacetylene and copolymer polyacetylene-polynorbornene

1992 ◽  
Vol 45 (16) ◽  
pp. 9439-9442 ◽  
Author(s):  
E. Mulazzi ◽  
A. Ripamonti ◽  
T. Verdon ◽  
S. Lefrant
1971 ◽  
Vol 25 (3) ◽  
pp. 355-360 ◽  
Author(s):  
J. L. Koenig ◽  
M. Itoga

A new method of measuring the absorbance corrected for orientation and the orientation of oriented polymer systems is derived. The method using unpolarized light utilizes a linear plotting and extrapolation technique to minimize experimental errors. The method is applied to oriented nlyon 66 samples and the results are compared with the previous methods.


In the past few years molecular engineering of liquid-crystalline (LC) polymers with respect to molecular architecture and functionalization has become increasingly important. Molecular architecture of LC polymers, i.e. the variation of the arrangement of mesogens, the variation of their shapes (rod, disc, board) and the variation of the polymer backbone, leads to polymers with new LC phases and new properties. Functionalized or dye-containing polymers can be used for a destruction or even the formation of the LC phase by photoreactions as well as for photochromic effects. The induction of discotic phases in amorphous polymers with disc-like mesogens is possible by charge-transfer interactions and opens the accessibility for a wide variety of highly oriented polymer systems.


1991 ◽  
Vol 41 (3) ◽  
pp. 1333-1336 ◽  
Author(s):  
E Mulazzi ◽  
G Leising ◽  
F Stelzer ◽  
T Verdon ◽  
S Lefrant

Author(s):  
J. Petermann ◽  
G. Broza ◽  
U. Rieck ◽  
A. Jaballah ◽  
A. Kawaguchi

Oriented overgrowth of polymer materials onto ionic crystals is well known and recently it was demonstrated that this epitaxial crystallisation can also occur in polymer/polymer systems, under certain conditions. The morphologies and the resulting physical properties of such systems will be presented, especially the influence of epitaxial interfaces on the adhesion of polymer laminates and the mechanical properties of epitaxially crystallized sandwiched layers.Materials used were polyethylene, PE, Lupolen 6021 DX (HDPE) and 1810 D (LDPE) from BASF AG; polypropylene, PP, (PPN) provided by Höchst AG and polybutene-1, PB-1, Vestolen BT from Chemische Werke Hüls. Thin oriented films were prepared according to the method of Petermann and Gohil, by winding up two different polymer films from two separately heated glass-plates simultaneously with the help of a motor driven cylinder. One double layer was used for TEM investigations, while about 1000 sandwiched layers were taken for mechanical tests.


Author(s):  
Barbara A. Wood

A controversial topic in the study of structure-property relationships of toughened polymer systems is the internal cavitation of toughener particles resulting from damage on impact or tensile deformation.Detailed observations of the influence of morphological characteristics such as particle size distribution on deformation mechanisms such as shear yield and cavitation could provide valuable guidance for selection of processing conditions, but TEM observation of damaged zones presents some experimental difficulties.Previously published TEM images of impact fractured toughened nylon show holes but contrast between matrix and toughener is lacking; other systems investigated have clearly shown cavitated impact modifier particles. In rubber toughened nylon, the physical characteristics of cavitated material differ from undamaged material to the extent that sectioning of heavily damaged regions by cryoultramicrotomy with a diamond knife results in sections of greater than optimum thickness (Figure 1). The detailed morphology is obscured despite selective staining of the rubber phase using the ruthenium trichloride route to ruthenium tetroxide.


1997 ◽  
Vol 48 (3) ◽  
pp. 463-472 ◽  
Author(s):  
R.P.T. JANSSEN ◽  
M.G.M. BRUGGENWERT ◽  
W.H. VAN RIEMSDIJK
Keyword(s):  

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