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6609958 
Journal Article 
Co-(POSS#-styrene) nanocomposites reduced the glass-transition temperature, rubbery modulus, and melt viscosity of entangled polystyrene 
Romo-Uribe, A; , 
2019 
1 
Polymer Engineering and Science
ISSN: 0032-3888
EISSN: 1548-2634 
WILEY 
HOBOKEN 
2377-2386 
WOS:000494612800020 
The addition of polyhedral oligomeric silsesquioxane-styrene copolymers, co(POSS#-sty), to entangled polystyrene (PS) reduced (1) the glass-transition temperature, T-g,T-blend, (2) the rubbery modulus, and (3) the melt viscosity. POSS#-sty copolymers with # = 15, 25, and 45 wt% POSS were blended with PS. The blends were miscible and T-g,T-blend decreased with POSS#-sty content. Strikingly, POSS#-sty copolymers also reduced the melt viscosity, up to an order of magnitude reduction. The reductions of T-g,T-blend and melt viscosity were driven by the type of POSS#-sty copolymer, POSS45-sty producing the largest decrease of T-g,T-blend. Linear viscoelasticity and the time-temperature superposition (TTS) principle (using T-ref = T-g + 50 K to ensure iso-frictional conditions) revealed that POSS#-sty induced up to an order of magnitude reduction of the rubbery modulus G(e). The increase of free volume f(g) promoted by POSS#-sty induced the reduction of T-g,T-blend and G(e), as revealed by TTS analysis. The increase of free volume promoted by POSS#-sty induced chain intercalation (TEM showed that POSS domains were smaller than the molecular mesh) and these are key factors for the chain disentanglement with the consequent rubbery modulus and melt viscosity reductions. The use of low-molecular weight polystyrene alone will not produce increase of free volume and tube dilation. POLYM. ENG. SCI., 2019. (c) 2019 Society of Plastics Engineers