Synthesis and Characterization of Nanoporous Silica Using Dendrimer Molecules

Abstract

A water soluble porogen, e.g., poly(amido amine) dendrimer, has been used as a structure-directing agent to introduce porosity of nanometer scale in silica-based nanocomposite materials. Hydrothermal synthesis was carried out at different elevated temperatures (343-413 K) in a closed teflon-lined stainless steel autoclave under autogenerated pressure. The synthesis time varied from 2 to 6 days, depending upon pH, synthesis temperature, concentration of porogen, etc. X-ray diffraction, transmission and scanning electron microscopic analyses, as well as infrared absorption spectroscopic measurements, were carried out to characterize these materials. Mostly disordered mesostructures were observed. The porous silica particles with sphere-like morphology varied from 30 to 200 nm in size were prepared depending upon the conditions of preparation. The structure and nanoporosity were preserved after the removal of structure-directing porogen through calcination at 823 K. The pore size was in the range of the dendrimer molecule as a template, indicating the structure-directing role of the terminal amino groups in the dendrimer molecule for the synthesis of nanoporous silica, since the nanoporous silica could be prepared by the hydrogen bonding or electrostatic interaction of dendrimer amino groups and tetraethyl orthosilicate.