Tris(3-(trimethoxysilyl)propyl)isocyanuratesilane was deposited from anhydr
ous methanol. The rate of deposition onto E-glass fibres, of this novel sil
ane, was determined by Si-29 NMR spectroscopy. During a 16-h treatment peri
od there was no evidence of hydrolysis or condensation of the silane soluti
on. The majority of the silane deposition occurred within the first few min
utes of the deposition process. Long deposition times resulted in large amo
unts of deposited silanes, which were easily dislodged when the fibres were
removed from the solution and dried. Given a coherent, highly ordered film
it was calculated that 1400 layers of isocyanuratesilane were deposited in
a 2% by weight silane solution. It is accepted, however, that silanes are
unlikely to deposit as a coherent layer, and condensation will disrupt any
previously ordered layers.
Solid state NMR indicated that isocyanuratesilane and a ureidosilane may ha
ve been bonded to E-glass fibres at a small number of surface SiO sites and
that from these locations a highly crosslinked siloxane polymer network wa
s formed. Industrial grade E-glass fibres were shown to have sufficient wat
er adsorbed onto the surface to induce hydrolysis and a high degree of cond
ensation at the E-glass surface.