This study focuses on understanding the growth and control of nanostructures using reverse micelles. It has been earlier realized that parameters like surfactant, cosurfactant, and aqueous content influence the size and shape of the nanostructures obtained using reverse micelles. However, a concerted effort to understand the role of these factors on the growth of a specific nanomaterial is missing. In this study we have focused on one nanomaterial (copper oxalate monohydrate) and determined how the above-mentioned factors control the size, shape, aspect ratio, and growth of these nanostructures. Our results show that cationic surfactants (CTAB, TTAB, and CPB) favor the formation of nanorods of copper oxalate. The aspect ratio of these rods could be controlled to obtain nanocubes (approximately 80-100 nm) and nanoparticles (approximately 8-10 nm) in the CTAB system using longer chain cosurfactants like 1-octanol and 1-decanol, respectively. Nanocubes of approximately 50-60 and approximately 60-80 nm were obtained using nonionic surfactants Triton X-100 and Tergitol, respectively. The size of the nanostructures could also be controlled by varying the molar ratio of water to surfactant (W0) by using a nonionic (Triton X-100)-based reverse micellar system. The study espouses the versatility of the microemulsion method to realize a variety of nanostructures of copper oxalate monohydrate. Our results will be of use in extending these ideas to other nanomaterials.
TiO2
sol was prepared hydrothermally in an autoclave from aqueous
TiOCl2
solutions as a starting precursor. Titanate nanotubes were obtained when the sol–gel-derived
TiO2
sol was treated chemically with a 10 M NaOH solution and subsequently heated in the autoclave at
150 °C
for 48 h. The samples were characterized using XRD, TEM, SEM, EDX, Raman
spectroscopy, and a BET surface area analyser. The effect of post treatments, such
as washing with and without hydrochloric acid and calcination, on the phase
structure, shape and morphology, pore structures, and BET surface area of the
titanate nanotubes was investigated. When a sample containing 7.08 wt% Na (after
washing only with water) was calcined at different temperatures from 300 to
900 °C, it showed the formation of a mixture of sodium trititanates and sodium hexatitanates
and was found to preserve the tubular morphology at higher temperatures.
However, a sample containing 0.06 wt% Na obtained after prolonged washing
with hydrochloric acid followed by heat treatment showed the formation of
TiO2 anatase
involving TiO2
(B) as an intermediate at lower temperatures and anatase was further transformed to the rutile
phase when the temperature was raised. On the basis of different observations, a general formula
NaxH2−xTi3O7·nH2O
has been proposed for the trititanate nanotubes.
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