1. Motivations
Colloidal
Gas Aphrons (or microfoams) can be used in numerous applications including oil
recovery, remediation of soils and waters contaminated with hydrocarbons, and
firefighting where foam is currently used. Unresolved questions remain regarding
the structure and rheology of CGA. The most widely accepted structure was
suggested by Sebba [1]. It speculates that bubbles have a multilayered shell
but no direct observation have demonstrated such a structure. Sebba [1] did not
elaborate on the thickness of the speculative soapy shell either.
2. Rheology of Colloidal Gas Aphrons
As
part of an undergraduate research project, the effect of surfactant
concentration and pipe shape and size on the rheological properties of
colloidal gas aphrons (CGA) or microfoams have been investigated. The effort
resulted in a publication [2]. In brief, pipe flow experiments
were performed in cylindrical pipes with various diameters. The porosity,
bubble size distribution, surface tension, and pH were systematically measured.
It was first established that there was no slip velocity at the wall and CGA did
not change morphology and porosity. Compressibility effects were
accounted for through the volume equalization approach [3]. To make the
experimental results more general, the volume equalized apparent shear rate and
shear stress are non-dimensionalized in terms of Capillary number Ca*
and dimensionless stress.
First,
Experiments where performed with pipe diameters 1., 1.5, and 2 mm and
surfactant Tween 20 mass fraction of 0.22 wt.%. It establishes that (1) CGA
can be considered as a shear thinning fluid, (2) the pipe shape and
diameter have no effect on the CGA rheology, (3) the dimensionless
volume equalized shear stress is proportional to (Ca*)m
where Ca* is the Capillary number and m = 0.65±0.06.
Furthermore,
the effect of concentration of surfactant on CGA rheology was assessed with various
aqueous solutions of Tween 20. The results are plotted in Fig. 2 in terms of
dimensionless shear stress as a function of volume equalized Capillary number
(Ca*)2/3 and show a linear relationship. Increase in shear stress with surfactant concentration at a given value of
Ca* could be attributed to the reduction in the maximum packing of
spherical bubbles as their size distribution narrows. As the maximum packing
decreases so does the viscosity.
3. CGA Morphology
It
is proposed to determine the morphology of CGA bubbles through scattering
technique based on depolarization of a polarized radiation as it travels
through the CGA. The experimental setup used to measure the scattered light
from CGA is shown in Figure 3 and described elsewhere [4]. A HeNe laser (632
nm) is employed as the light source. A flow cells is used to flow the freshly
generated CGA through the beam. The experimental apparatus and procedure were successfully
validated using polystyrene microspheres. Then, experiments with CGA were
performed with surfactant concentration of 2 ml Tween-20 per liter of deionized
water. The flow cell thickness was 0.2-0.5 mm. The intensity vector is defined
as (I,Q,U,V)T where I is the total intensity, Q represents the
tendency for horizontal polarization, U the tendency for ± 45° polarization, and
V for circular polarization. The scattered intensity vector is related to the
incident intensity vector through the Mueller matrix as [4]. The scattering
Mueller matrix element S11 relates to total intensity, S12
to the linear polarization, S22 represent the deviation of the scatterers'
shape from sphericity (for perfect spheres S11=S22), and S34
corresponds to the transformation from circular to linear polarization. The collected
data was normalized with their value at scattering angle of 5 degree. The
experimental data collected during the reporting period are of very good
quality given the strongly scattering nature of CGA and the sensitivity of the
measurements. However, the physical phenomena responsible such as dependent
scattering and theoretical analysis are quite complex. Development of a
theoretical model accounting for dependent scattering due to the close
proximity of bubbles in CGA is currently under way.
4.
References
[1] Sebba,
F., 1987. Wiley & Sons, New York.
[2] S.
Larmignat, D. Vanderpool, H. Lai, and L. Pilon, 2008. Colloids and Surfaces A: http://dx.doi.org/10.1016/j.colsurfa.2008.03.010
.
[3] P. Valko and M.J. Economides, 1992. Journal
of Rheology, (36), 111-127.
[4] M.M. Aslan, C. Crofcheck,
D. Tao, and M. Pinar Menguc, 2006. Journal of Quantitative Spectroscopy and Radiation
Transfer, (101), 527-539.