Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-29T19:02:36.041Z Has data issue: false hasContentIssue false

Morphology Study of Polystyrene-Polybutadiene-polycaprolactone (PS-b-PB-b-PCL), Polybutadiene-Polycaprolactone (PB-b-PCL), and Polystyrene-Polycaprolactone (PS-b-PCL) Semicrystalline Block Copolymers

Published online by Cambridge University Press:  02 July 2020

G. Kim
Affiliation:
National Institute of Standards and Technology, Gaithersburg, MD20899
C. L. Jackson
Affiliation:
National Institute of Standards and Technology, Gaithersburg, MD20899
F. v. Gyldenfeldt
Affiliation:
Universitaet Bayreuth, Bayreuth, Germany
V. Balsamo
Affiliation:
Universidade Simon Bolivar, Carcas, Venezuela
M. Libera
Affiliation:
Stevens Institute of Technology, Hoboken, NJ07030
R. Stadler
Affiliation:
Universitaet Bayreuth, Bayreuth, Germany
C. C. Han
Affiliation:
National Institute of Standards and Technology, Gaithersburg, MD20899
Get access

Extract

Semicrystalline block copolymers containing one crystalline block, such as PCL, show more complicated morphologies than amorphous block copolymers. This is because the microstructure of semicrystalline block copolymers is determined by the interplay between the microphase-separation temperature, crystallization temperature, and glass transition temperatures of the respective blocks. This paper describes initial results of thermodynamic and kinetic effects associated with microphase separation and crystallization in as-cast semicrystalline (PS)0.62(PCL)0.38, (PB)0.2(PCL)0.8 and (PS)0.35(PB)0.15(PCL)0.5 block copolymers, where the subscripts denote the mass fraction of each block.

Semicrystalline block copolymers (PS-b-PCL with Mn=209,000 g/mol, PB-b-PCL with Mn=146,000 g/mol and PS-b-PB-b-PCL with Mn= 150,000 g/mol) were prepared by anionic polymerization. Films were cast from 5% (mass fraction) solutions in toluene into ∼lmm thick films. A relatively slow solvent evaporation over approximately a 10 d period was achieved by partially covering the dishes containing polymer solutions.

Type
Developments in Measuring Polymer Microstructures
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Balsamo, V., von Gyldenfeldt, F., and Stadler, R., Macromol. Chem. Phys. 197 (1996) 1159.CrossRefGoogle Scholar

2. Balsamo, V., von Gyldenfeldt, F., and Stadler, R., Macromol. Chem. Phys. 197 (1996) 3317.CrossRefGoogle Scholar

3. Cohen, R., Cheng, P., Douzinas, K., Kofinas, K., and Berney, V., Macromol. 23 (1990) 324.CrossRefGoogle Scholar

4. Heuschen, J., Jerome, R., and Teyssie, P.,: Part B: Poly. Phys. J. Poly. Sci. 27 (1989) 523.CrossRefGoogle Scholar

5. S. Nojima, , K. Kato, , S. Yamamoto, , and T. Ashida, , Polymer J. 27 (1995) 673.CrossRefGoogle Scholar

6. Nojima, S., Nakano, J., Takahashi, Y., Ahida, T., Polymer 35 (1994) 3479.CrossRefGoogle Scholar

7. Nojima, S., Kato, K., Yamamoto, S., Ashida, T., Macromol. 25 (1992) 2237.CrossRefGoogle Scholar