Domain Growth and Wetting in a Low Molecular Weight Binary Fluid System

1991 ◽  
Vol 237 ◽  
Author(s):  
Bill Q. Shi ◽  
Andrew W. Cumming

AbstractWe present the results of phase-separation experiments performed on the pseudo-binary fluid system guaiacol-glycerol-water. Elastic light scattering and optical microscopy were used to follow the phase-separation after quenches into the coexistence region of the phase diagram. For critical quenches, we observed the well known bicontinuous infinite cluster morphology normally associated with spinodal decomposition, but with two distinct growth modes. In the bulk, at early times we observed L(t) ∼ t1/3 consistent with diffusion driven dynamics, crossing over to L(t) ∼ t1 at later times, as hydrodynamics became important. Near the sample walls, there obtained a novel fast growth with L(t) ∼ t3/2, just as in the case of recent studies with polymer blends, inconsistent with either diffusion or interface driven dynamics. We attribute this large exponent to wetting effects, and the observation of the same phenomenon in such disparate systems as polymer blends and polar organic solvents is strong evidence that the phenomenon is generic to binary systems.

1991 ◽  
Vol 248 ◽  
Author(s):  
Andrew W. Cumming ◽  
Pierre Wiltzius

AbstractWe present the results of phase-separation experiments performed on the binary polymer blend polyisoprene-poly(ethylene-propylene). Elastic light scattering and optical microscopy were used to follow the phase-separation after quenches into the coexistence region of the phase diagram. For critical quenches, we observed the well known bicontinuous infinite cluster morphology normally associated with spinodal decomposition, but with two distinct growth modes. In the bulk, we observed L(t) - t1/3 consistent with diffusion driven dynamics, whereas near the sample walls, there obtained a novel fast growth with L(t) -t 3/2, inconsistent with either diffusion or interface driven dynamics. We attribute this large exponent to wetting effects, but still lack any theoretical understanding of the phenomenon.


1996 ◽  
Vol 461 ◽  
Author(s):  
S. Kim ◽  
C. C. Han

ABSTRACTThe effect of diblock copolymer on the phase-separation process of polymer blends has been investigated by using light scattering and optical microscopic observations. To quench the system into the two phase region, a shear-jump technique is employed instead of the conventional temperature-jump technique. The samples studied are blends of low-molecular-weight polystyrene and polybutadiene with and without added styrene-butadiene block copolymer as a compatibilizer. It was observed that the addition of diblock copolymers could accelerate the phase separation kinetics depending on the shear history. As the concentration of diblock copolymer increases, the distribution of domain sizes becomes narrower and the growth rate slows down. The extent of slowing-down depends on the molecular weight and concentration of the copolymer. The time dependence of domain growth is clearly observed with optical microscopy.


Kobunshi ◽  
1992 ◽  
Vol 41 (11) ◽  
pp. 790-793
Author(s):  
Hajime Tanaka

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 773
Author(s):  
Ahmad Safwan Ismail ◽  
Mohammad Jawaid ◽  
Norul Hisham Hamid ◽  
Ridwan Yahaya ◽  
Azman Hassan

Polymer blends is a well-established and suitable method to produced new polymeric materials as compared to synthesis of a new polymer. The combination of two different types of polymers will produce a new and unique material, which has the attribute of both polymers. The aim of this work is to analyze mechanical and morphological properties of bio-phenolic/epoxy polymer blends to find the best formulation for future study. Bio-phenolic/epoxy polymer blends were fabricated using the hand lay-up method at different loading of bio-phenolic (5 wt%, 10 wt%, 15 wt%, 20 wt%, and 25 wt%) in the epoxy matrix whereas neat bio-phenolic and epoxy samples were also fabricated for comparison. Results indicated that mechanical properties were improved for bio-phenolic/epoxy polymer blends compared to neat epoxy and phenolic. In addition, there is no sign of phase separation in polymer blends. The highest tensile, flexural, and impact strength was shown by P-20(biophenolic-20 wt% and Epoxy-80 wt%) whereas P-25 (biophenolic-25 wt% and Epoxy-75 wt%) has the highest tensile and flexural modulus. Based on the finding, it is concluded that P-20 shows better overall mechanical properties among the polymer blends. Based on this finding, the bio-phenolic/epoxy blend with 20 wt% will be used for further study on flax-reinforced bio-phenolic/epoxy polymer blends.


Author(s):  
Adriano Tiribocchi ◽  
Antonio Piscitelli ◽  
Giuseppe Gonnella ◽  
Antonio Lamura

1996 ◽  
Vol 101 (1) ◽  
pp. 157-165 ◽  
Author(s):  
Charles C. Han

2006 ◽  
Vol 37 (3) ◽  
pp. 328-335 ◽  
Author(s):  
Tuyet L. Tran ◽  
Philip K. Chan ◽  
Derick Rousseau

1993 ◽  
Vol 48 (5) ◽  
pp. 3705-3711 ◽  
Author(s):  
Gregory Brown ◽  
Amitabha Chakrabarti

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