6533b7ddfe1ef96bd12753a3

RESEARCH PRODUCT

PMMA-titania nanocomposites: Properties and thermal degradation behavior

T.e. MotaungAdriaan S. LuytMaria Luisa SaladinoEugenio CaponettiAlberto SpinellaFederica BondioliGiorgio NasilloMassimo Messori

subject

Thermogravimetric analysisAnataseMaterials sciencePolymers and Plasticslaw.inventionlawnanocompositesPMMA Titania Nanocomposites Interfacial interaction Properties Degradation kineticsMaterials ChemistrytitaniaCalcinationFourier transform infrared spectroscopyComposite materialSettore CHIM/02 - Chimica Fisicachemistry.chemical_classificationNanocompositePolymerDynamic mechanical analysisCondensed Matter PhysicsPMMAAmorphous soliddegradation kineticsChemical engineeringchemistryMechanics of MaterialspropertiesPMMA; titania; nanocomposites; interfacial interaction; properties; degradation kineticsinterfacial interaction

description

Titania nanoparticles were prepared using a solegel method and calcination at 200 and 600 � C in order to obtain anatase and rutile phases, respectively. The obtained powders were used to prepare PMMAe titania nanocomposites by a melt compounding method. The effect of the crystalline phase and the amount of titania, in the range 1e5 wt.%, on the morphology, mechanical properties and thermal degradation kinetics of PMMA was investigated by means of X-ray diffractometry (XRD), transmission electron microscopy (TEM), 13 C cross-polarization magic-angle spinning nuclear magnetic resonance spectroscopy ( 13 C{ 1 H}CP-MAS NMR), including the measurement of proton spinelattice relaxation time in the rotating frame (T1r(H)), in the laboratory frame (T1(H)) and cross polarization times (TCH), and dynamic mechanical analysis (DMA), thermogravimetric analysis (TGA), and Fourier-transform infrared (FTIR) spectroscopy. Results showed that both types of titania were well dispersed in the polymeric matrix, whose structure remained amorphous. The two types of nanoparticles influenced the degrada- tion of the polymer in different ways because of their different carbon content, particle size and crystal structures.

10.1016/j.polymdegradstab.2012.05.022http://hdl.handle.net/10447/74773