Nanocomposites of polymers and inorganic fillers represent a class of materials of great interest for many practical applications. Polyvinylbutyral (PVB) is an amorphous polymer employed in automotive and architectural applications for laminated safety glasses thanks to its high binding efficiency, optical clarity, and good adhesion to several different surfaces. Additional interesting properties for glass construction can be obtained using PVB as a matrix in nanocomposite materials. Indeed, loading PVB with Antimony Tin Oxide (ATO) nanoparticles makes the material capable of filtering out the near infrared (NIR) waves of sunlight while maintaining transmission in the visible region. This property is becoming of relevance in building and vehicle glass construction as a consequence of the worldwide energy saving and environmental preservation policies. In view of the optimization of PVB-ATO nanocomposite formulation for applicative purposes a thorough characterization of structural and dynamic microscopic properties of these materials is necessary. In this study the effects of loading PVB with ATO nanoparticles on the polymer dynamics were investigated combining high resolution solid state 13C NMR spectroscopy and low resolution 1H NMR relaxometry. In particular, 1H longitudinal relaxation times (T1) were measured in the 0.01 to 35 MHz frequency range by Fast Field Cycling NMR relaxometry, whereas 1H transversal relaxation times (T2) were determined by Free Induction Decay (FID) analysis at 20 MHz. All experiments were performed on both PVB and PVB-ATO in the temperature range between 30 and 120 °C, the polymer glass transition occurring at about 70 °C. The analyses of the dispersion curves and FIDs showed that loading with ATO nanoparticles results in an increase in polymer mobility. A comparative study with broadband dielectric relaxation spectroscopy, in a frequency range up to 10 MHz, helped to elucidate peculiar features due to random blocks of polyvinylalcohol and polyvinylbutyral present in the polymer structure. Local dielectric spectroscopy (LDS) experiments were also performed close to the glass transition to highlight changes in the polymer dynamic behavior at the interface with the nanoparticles.
Investigation of polymer dynamics in PVB-ATO nanocomposites by NMR relaxometry and dielectric relaxation spectroscopy
Silvia Pizzanelli;Claudia Forte;Simona Bronco;Massimiliano Labardi;Lucia Calucci
2015
Abstract
Nanocomposites of polymers and inorganic fillers represent a class of materials of great interest for many practical applications. Polyvinylbutyral (PVB) is an amorphous polymer employed in automotive and architectural applications for laminated safety glasses thanks to its high binding efficiency, optical clarity, and good adhesion to several different surfaces. Additional interesting properties for glass construction can be obtained using PVB as a matrix in nanocomposite materials. Indeed, loading PVB with Antimony Tin Oxide (ATO) nanoparticles makes the material capable of filtering out the near infrared (NIR) waves of sunlight while maintaining transmission in the visible region. This property is becoming of relevance in building and vehicle glass construction as a consequence of the worldwide energy saving and environmental preservation policies. In view of the optimization of PVB-ATO nanocomposite formulation for applicative purposes a thorough characterization of structural and dynamic microscopic properties of these materials is necessary. In this study the effects of loading PVB with ATO nanoparticles on the polymer dynamics were investigated combining high resolution solid state 13C NMR spectroscopy and low resolution 1H NMR relaxometry. In particular, 1H longitudinal relaxation times (T1) were measured in the 0.01 to 35 MHz frequency range by Fast Field Cycling NMR relaxometry, whereas 1H transversal relaxation times (T2) were determined by Free Induction Decay (FID) analysis at 20 MHz. All experiments were performed on both PVB and PVB-ATO in the temperature range between 30 and 120 °C, the polymer glass transition occurring at about 70 °C. The analyses of the dispersion curves and FIDs showed that loading with ATO nanoparticles results in an increase in polymer mobility. A comparative study with broadband dielectric relaxation spectroscopy, in a frequency range up to 10 MHz, helped to elucidate peculiar features due to random blocks of polyvinylalcohol and polyvinylbutyral present in the polymer structure. Local dielectric spectroscopy (LDS) experiments were also performed close to the glass transition to highlight changes in the polymer dynamic behavior at the interface with the nanoparticles.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.