ABSTRACTSilica aerogels have numerous properties which suggest applications such as
ultra high efficiency thermal insulation. These properties relate directly
to the aerogel's pore size distribution. The micro and meso pore size ranges
can be investigated by normal small angle x-ray scattering and possibly,
nitrogen adsorption. However, the measurement of larger pores (> 250 Å)
is more difficult. Due to their limited mechanical strength, mercury
porosimetry and nitrogen condensation can disrupt the gel structure and
electron microscopy provides only limited large scale structure information.
The use of small angle light scattering techniques seems to have promise,
the only hurdle is that aerogels exhibit significant multiple scattering.
This can be avoided if one observes the gels in the wet stage since the
structure of the aerogel should be very similar to the wet gel (as the
result of supercritical drying). Thus, if one can match the refractive
index, the morphology can be probed. The combination of certain alcoholic
solvents fit this index matching criteria. Preliminary results for the gel
network (micron range) and primary particle structure (nanometer) are
reported by using small angle light scattering and ultra-small angle x-ray
scattering. The effects on structure over the length scale range of <1 nm
to >5 μπι under different conditions (precursors, pH, etc.) are
presented. The change in structure of an aerogel during isostatic compaction
to 228 MPa (to simulate drying from wetting solvents) are also
discussed.
Arguments for an additional long-lived intermediate in the photocycle of the full-length aureochrome 1c receptor: A time-resolved small-angle X-ray scattering study