We report a "delayed neutralization" process for the preparation of highly-
ordered aluminosilicate MCM-41 molecular sieves with high thermal and hydro
thermal stability, and sharp pore size distribution. However, the structura
l order and pore size are dependent on the carbon chain length. In the mixt
ure surfactant systems, the pore size of the MCM-41 materials could be fine
-tuned. The pore size can be extended from 2.5 to 4.5 nm by adding a suitab
le amount of hydrocarbons. The tubular morphology of the MCM-41 material of
0.3 to 10 micrometers diameter, where the wall consists of coaxial cylindr
ical pores of nanometers MCM-41, can be obtained by careful control of the
surfactant-water content and the rate of condensation of silica. An optimum
condition for automatic synthesis of the hierarchical TWT structure has be
en accomplished. The addition of I-alkanols as cosurfactant would not only
improve the order of the MCM-41 hexagonal structure but also promote the fo
rmation of micrometer-sized hierarchical materials, for example: tubules-wi
thin-tubule and uniform-sized hollow spheres of diameter 5.0 +/- 1.0 mu m.
However, the inside of the micron spheres has intricate structures possessi
ng various topological genus ranks. The MCM-41 is a good supporter for Moly
bdenum oxide catalysts. The rate of deactivation in the catalytic reaction
of ethyl benzene dehydrogenation to styrene increases in the order: M-tau <
M-p < SiO2. The physically mixed samples have higher catalytic activity th
an impregnated ones.