Synthesis and characterization of transparent alumina reinforced polycarbonate nanocomposite

Transparent nanocomposite films were fabricated by blending a concentrated nanocomposite formed by in-situ polymerization of polycarbonate in the presence of alumina nanowhisker with a high molecular weight polycarbonate. Polycarbonate was grafted to the alumina nanowhisker surface to improve nanofi...

Full description

Saved in:
Bibliographic Details
Published inPolymer (Guilford) Vol. 51; no. 12; pp. 2494 - 2502
Main Authors Hakimelahi, Hamid R., Hu, Ling, Rupp, Bradley B., Coleman, Maria R.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 28.05.2010
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Transparent nanocomposite films were fabricated by blending a concentrated nanocomposite formed by in-situ polymerization of polycarbonate in the presence of alumina nanowhisker with a high molecular weight polycarbonate. Polycarbonate was grafted to the alumina nanowhisker surface to improve nanofiller dispersion and load transfer to polymer matrix. Fourier transform infrared spectroscopy confirmed the functionalization of the nanowhisker with polycarbonate. Samples produced using functionalized alumina exhibited improved dispersion compared to the raw alumina nanowhiskers in the PC. Functionalization of alumina nanowhisker enhanced tensile properties (Young’s modulus and tensile strength) relative to the pure polycarbonate and blends produced with raw alumina nanowhisker. Additionally, the nanocomposite formed using in-situ polymerization showed small decreases in transparency in the visual range compared to the base polymer with increased absorption in the UV range. The effect of reaction temperature during in-situ polymerization on the properties of the nanocomposite was investigated. Higher reaction temperature resulted in improved dispersion and sharp increases in tensile modulus and shear strength. Graphical abstract [Display omitted]
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2010.04.023