A miscibility study of ternary blends of polystyrene, tetramethylbisphenol-A polycarbonate, and poly(2,6-dimethyl-1,4-phenylene oxide)

1994 ◽  
Vol 1 (3) ◽  
pp. 227-234 ◽  
Author(s):  
A. C. Su ◽  
J. R. Fried
Author(s):  
S.D. Smith ◽  
R.J. Spontak ◽  
D.H. Melik ◽  
S.M. Buehler ◽  
K.M. Kerr ◽  
...  

When blended together, homopolymers A and B will normally macrophase-separate into relatively large (≫1 μm) A-rich and B-rich phases, between which exists poor interfacial adhesion, due to a low entropy of mixing. The size scale of phase separation in such a blend can be reduced, and the extent of interfacial A-B contact and entanglement enhanced, via addition of an emulsifying agent such as an AB diblock copolymer. Diblock copolymers consist of a long sequence of A monomers covalently bonded to a long sequence of B monomers. These materials are surface-active and decrease interfacial tension between immiscible phases much in the same way as do small-molecule surfactants. Previous studies have clearly demonstrated the utility of block copolymers in compatibilizing homopolymer blends and enhancing blend properties such as fracture toughness. It is now recognized that optimization of emulsified ternary blends relies upon design considerations such as sufficient block penetration into a macrophase (to avoid block slip) and prevention of a copolymer multilayer at the A-B interface (to avoid intralayer failure).


2020 ◽  
Vol 35 (2) ◽  
pp. 169-183 ◽  
Author(s):  
P. Hadimani ◽  
H. N. Narasimha Murthy ◽  
R. Mudbidre
Keyword(s):  
Nylon 6 ◽  

2021 ◽  
Vol 624 ◽  
pp. 119088
Author(s):  
Lv Li ◽  
Jiaao Wang ◽  
Manzoor Hussain ◽  
Lingling Ma ◽  
Naeem Akhtar Qaisrani ◽  
...  

2011 ◽  
Vol 23 (35) ◽  
pp. 4093-4097 ◽  
Author(s):  
Toby A. M. Ferenczi ◽  
Christian Müller ◽  
Donal D. C. Bradley ◽  
Paul Smith ◽  
Jenny Nelson ◽  
...  
Keyword(s):  

Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2372
Author(s):  
Yesenia Sánchez-Cardona ◽  
Claudia E. Echeverri-Cuartas ◽  
Marta E. Londoño López ◽  
Natalia Moreno-Castellanos

Chitosan scaffolds based on blending polymers are a common strategy used in tissue engineering. The objective of this study was evaluation the properties of scaffolds based on a ternary blend of chitosan (Chi), gelatin (Ge), and polyvinyl alcohol (PVA) (Chi/Ge/PVA), which were prepared by cycles of freeze-thawing and freeze-drying. It then was used for three-dimensional BRIN-BD11 beta-cells culturing. Weight ratios of Chi/Ge/PVA (1:1:1, 2:2:1, 2:3:1, and 3:2:1) were proposed and porosity, pore size, degradation, swelling rate, compressive strength, and cell viability analyzed. All ternary blend scaffolds structures are highly porous (with a porosity higher than 80%) and interconnected. The pore size distribution varied from 0.6 to 265 μm. Ternary blends scaffolds had controllable degradation rates compared to binary blend scaffolds, and an improved swelling capacity of the samples with increasing chitosan concentration was found. An increase in Young’s modulus and compressive strength was observed with increasing gelatin concentration. The highest compressive strength reached 101.6 Pa. The MTT assay showed that the ternary blends scaffolds P3 and P4 supported cell viability better than the binary blend scaffold. Therefore, these results illustrated that ternary blends scaffolds P3 and P4 could provide a better environment for BRIN-BD11 cell proliferation.


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