On the excess volume in polymer blends

Polymer ◽  
1991 ◽  
Vol 32 (3) ◽  
pp. 501-504 ◽  
Author(s):  
Hans-Werner Kammer
Keyword(s):  
Author(s):  
E. G. Rightor

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.


Author(s):  
William A. Heeschen

Two new morphological measurements based on digital image analysis, CoContinuity and CoContinuity Balance, have been developed and implemented for quantitative measurement of morphology in polymer blends. The morphology of polymer blends varies with phase ratio, composition and processing. A typical morphological evolution for increasing phase ratio of polymer A to polymer B starts with discrete domains of A in a matrix of B (A/B < 1), moves through a cocontinuous distribution of A and B (A/B ≈ 1) and finishes with discrete domains of B in a matrix of A (A/B > 1). For low phase ratios, A is often seen as solid convex particles embedded in the continuous B phase. As the ratio increases, A domains begin to evolve into irregular shapes, though still recognizable as separate domains. Further increase in the phase ratio leads to A domains which extend into and surround the B phase while the B phase simultaneously extends into and surrounds the A phase.


Polymer News ◽  
2005 ◽  
Vol 30 (9) ◽  
pp. 296-300
Author(s):  
F. Esposito ◽  
V. Casuscelli ◽  
M. V. Volpe ◽  
G. Carotenuto ◽  
L. Nicolais

1990 ◽  
Vol 51 (2) ◽  
pp. 185-200 ◽  
Author(s):  
Zhen-Gang Wang ◽  
S.A. Safran

1989 ◽  
Vol 50 (3) ◽  
pp. 245-253 ◽  
Author(s):  
M.G. Brereton ◽  
T.A. Vilgis
Keyword(s):  

2003 ◽  
Vol 18 (2) ◽  
pp. 151-155 ◽  
Author(s):  
L. S. Pinchuk ◽  
V. A. Goldade ◽  
A. G. Kravtsov ◽  
S. V. Zotov ◽  
B. Jurkowski ◽  
...  

1979 ◽  
Vol 44 (2) ◽  
pp. 295-306 ◽  
Author(s):  
Ivan Cibulka ◽  
Vladimír Hynek ◽  
Robert Holub ◽  
Jiří Pick

A digital vibrating-tube densimeter was constructed for measuring the density of liquids at several temperatures. The underlying principle of the apparatus is the measurement of the period of eigen-vibrations of a V-shaped tube; the second power of the period of the vibrations is proportional to the density of the liquid in the tube. The temperature of the measuring system is controlled by an electronic regulator. The mean error in the density measurement is approximately ±1 . 10-5 g cm-3 at 25 °C and ±2 . 10-5 g cm-3 at 40 °C. The apparatus was used for an indirect measurement of the excess volume, tested with the benzene-cyclohexane system and further used for determining the excess volume of the benzene-methanol, benzene-acetonitrile and methanol-acetonitrile systems at 25 and 40 °C.


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