Linear viscoelasticity of blends of polybutadiene and highly hydrogenated polybutadiene
The linear viscoelastic behavior of a series of partially hydrogenated polybutadienes (PHPB) obtained by catalytic hydrogenation of an almost monodisperse polybutadiene (PB) was studied experimentally at temperatures above 110°C. The molecular characterization of the polymers used in this study show...
| Autores: | , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2000 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/37651 |
| Acceso en línea: | http://hdl.handle.net/11336/37651 |
| Access Level: | acceso abierto |
| Palabra clave: | Polybutadiene Hydrogenation Linear Viscoelasticity Blends https://purl.org/becyt/ford/2.5 https://purl.org/becyt/ford/2 |
| Sumario: | The linear viscoelastic behavior of a series of partially hydrogenated polybutadienes (PHPB) obtained by catalytic hydrogenation of an almost monodisperse polybutadiene (PB) was studied experimentally at temperatures above 110°C. The molecular characterization of the polymers used in this study showed that the catalytic hydrogenation of PB produces materials with a bimodal distribution of polymer species for global conversions lower than approximately 90%. All the PHPBs, even the less hydrogenated, are a mixture of a highly hydrogenated PB (with approximately 89% saturation) and unreacted PB. The rheological behavior of the fluids was studied measuring the elastic and viscous moduli at different temperatures in small-amplitude oscillatory shear flow. The two-phase polymer blends show thermorheological complex behavior and an increase in elasticity at low frequencies which may be associated with long relaxation time processes. The dynamic moduli of the pure components in the terminal region is modeled using a single relaxation time while the blends are described by a minimum of three relaxation modes. The two smaller relaxation times correspond to the relaxation of the blend components while the largest comes from the geometric relaxation of the shape of the interface. The zero-shear-rate viscosity of the PHPBs shows a positive deviation relative to log-additivity rule. But, when the predicted contribution of the interface is subtracted, the resulting zero-shear-rate viscosity as a function of the concentration follows this rule. © 2000 The Society of Rheology. |
|---|