Three commercial clays: Cloisite Na+
, Cloisite 30B and Cloisite 15A were used to
melt compound with a number of polymer matrices, including polypropylene (PP),
poly(butylene terephthalate) (PBT) and polyamides (PA). X-ray diffraction (XRD),
contact angle measurement and thermogravimetric analysis (TGA) showed small
interlayer space, poor compatibility and low thermal stability of these
nanocomposites, resulting in poor mechanical properties in composites. A number of
modifications of commercial clays were carried out, including silylation and
introduction of thermally stable surfactants, e.g. alkyl quaternary phosphonium
cations and polyhedral oligomeric silsesquioxane (POSS). It was found that poor
compatibility between polymer matrices and organically modified clays, especially
in those POSS modified clays, again restricted the formation of exfoliated structure
in polymer matrices. A mode of dual-surfactant modification for clay was developed,
and large interlayer spacing (>3.2 nm), good thermal stability (decomposed at
~300ºC) and improved surface properties for those dual-surfactant modified clays
promoted a better dispersion of clays in polymer matrices and consequently better
mechanical properties. For example, the tensile moduli of PP, PBT and PA 12 were
improved from 515 MPa, 1065 MPa and 490 MPa to 1020 MPa, 1470 MPa and 800
MPa of their nanocomposites containing 3 wt% dual-surfactant modified clays,
respectively. However, the dispersion of these organoclays varied in different
polymer matrices, due to the different compatibility and the existence of polar type
interactions between organoclays and polymer matrices. In order to further address
the effect of polymer matrix on clay dispersion, three polyamide matrices (PA 6, PA
11 and PA 12) were employed, and PA 6 based nanocomposites showed the most
effective exfoliation and mechanical enhancements due to the strong polar type
interactions between the polymer and the organoclays.
History
School
Aeronautical, Automotive, Chemical and Materials Engineering