Polystyrene crosslinked with oligomeric and polymeric poly(dimethyl siloxane) derivatives. Thermal and dynamic mechanical studies

Heikki Tenhu, Eeva‐Leena Heino

Journal of Applied Polymer Science · 1992 · 34 citations · 16 references

Concepts

Abstract

Abstract Styrene has been copolymerized with various bifunctional poly(dimethyl siloxane) cross‐linkers having molar masses in the range 200–35,000. Calorimetric and rheological measurements show that the crosslinkers change T g , T ll , and T exo , as well as melt viscosity and elasticity of polystyrene. These changes are strongly dependent on the molar mass of the crosslinker. Increasing the length of the siloxane crosslinker lowers T g and melt viscosity, if the molar mass of the crosslinker is in a range 200–2000. Copolymerizing styrene with a bifunctional poly(dimethyl siloxane) having molar mass near 35,000 leads to a phase‐separated polymer where polystyrene phase largely retains its original properties.

References

16