M. Yada et al., SYNTHESIS OF ALUMINUM-BASED SURFACTANT MESOPHASES MORPHOLOGICALLY CONTROLLED THROUGH A LAYER TO HEXAGONAL TRANSITION, Inorganic chemistry, 36(24), 1997, pp. 5565-5569
The morphologically controlled synthesis of aluminum-based surfactant
mesophases by the homogeneous precipitation method using urea is demon
strated, together with a model for the templating mechanism pathway. D
odecyl sulfate surfactant initially forms a layered mesophase with an
interlayer spacing of 3.5 nm in which the surfactant molecules are arr
anged as a bilayer between the linked sheets of aluminum oxyhydroxide
groups. The aluminate sheets consist mostly of octahedral Al but conta
in some fraction of tetrahedral Al dependent on urea concentration. On
further hydrolysis of urea, the layered mesophase is transformed into
a hexagonal form through the interlayer condensation and cross-linkin
g of the Al-OH groups in any adjacent aluminate sheets. The structural
transition accompanies the rearrangement of the bilayered surfactant
molecules into a rodlike assembly, followed by the additional growth i
nto enlarged particles. The hexagonal mesophase resulting from the lam
ellae containing comparatively large amounts of tetrahedral Al forms a
ringed or curved wormlike morphology, while the phase grown from octa
hedral Al-enriched forms appears in versatile patterns including spher
ical, funneled, and tubular particles. Such morphologically versatile
characteristics of the hexagonal mesophases reflect those of their pre
cursors produced by the folding of aluminum-based flexible sheets of a
luminum oxyhydroxide octahedral groups mixed with their tetrahedral on
es at a fraction dependent on urea concentration.