• Muller, Alejandro
• Múgica, Agurtzane
• Zubitur, Manuela
• Maspoch, Maria Lluisa
• Matxinandiarena, Eider
• Irusta, Silvia
• Yus Argón, Cristina
• Santana Pérez, Orlando
• Loaeza, Alfonso David

Abstract

<jats:p>Titanium dioxide (TiO2) nanoparticles have recently appeared in PET waste because of the introduction of opaque PET bottles. We prepare polymer blend nanocomposites (PBNANOs) by adding hydrophilic (hphi), hydrophobic (hpho), and hydrophobically modified (hphoM) titanium dioxide (TiO2) nanoparticles to 80rPP/20rPET recycled blends. Contact angle measurements show that the degree of hydrophilicity of TiO2 decreases in the order hphi &gt; hpho &gt; hphoM. A reduction of rPET droplet size occurs with the addition of TiO2 nanoparticles. The hydrophilic/hydrophobic balance controls the nanoparticles location. Transmission electron microscopy (TEM_ shows that hphi TiO2 preferentially locates inside the PET droplets and hpho at both the interface and PP matrix. HphoM also locates within the PP matrix and at the interface, but large loadings (12%) can completely cover the surfaces of the droplets forming a physical barrier that avoids coalescence, leading to the formation of smaller droplets. A good correlation is found between the crystallization rate of PET (determined by DSC) and nanoparticles location, where hphi TiO2 induces the highest PET crystallization rate. PET lamellar morphology (revealed by TEM) is also dependent on particle location. The mechanical behavior improves in the elastic regime with TiO2 addition, but the plastic deformation of the material is limited and strongly depends on the type of TiO2 employed.</jats:p>

Topics

• nanoparticle
• nanocomposite
• impedance spectroscopy
• dispersion
• surface
• transmission electron microscopy
• differential scanning calorimetry
• titanium
• forming
• crystallization
• polymer blend