Reservoir Engineering: Contact Angle Measurement
1. To what extent, the ‘gravitational force’ plays a crucial role:
(a) when the fluid flow remains to be perfectly horizontal;
(b) when the fluid flow remains to be perfectly vertical;
(c) when the fluid flows at an angle towards gravity; and
(d) when the fluid flows at an angle against gravity; - towards dictating whether
(i) the cohesive forces between the liquid molecules remain to be stronger than the adhesive forces between the solid and liquid molecules (and as a result, the liquid balls up and tending to avoid contact with the surface); or,
(ii) the solid/liquid adhesion remaining stronger than the cohesion within the liquid molecules (and as a result, no drop forms and the liquid tending to spread on the surface)?
Whether such role of ‘gravity’ would remain to be similar both @ laboratory-scale as well as @ field-scale?
If not, how would ‘contact angle’ measured @ laboratory-scale would be able to provide ‘an inverse measure of wettability’ @ field-scale?
2. In the absence of an atomically flat and chemically homogenous ideal surface – associated with a real field reservoir scenario; (for that matter, even with laboratory-scale experimental conditions), whether force per unit length OR energy per unit area would remain to be more apt towards the determination of contact angles (where, the formation of a perfect spherical cap geometry remains ruled out)?
3. Which one of the following essentially controls the wettability @ laboratory-scale? (a) the advancement of solid/liquid interface to a certain area; OR (b) the advancement of three-phase contact line to a certain length; upon placing a sessile droplet on a substrate?
4. Which one of them plays a very crucial role in ceasing the apparent contact angle @ field-scale?
(a) the surface roughness;
(b) the chemical heterogeneity of surface; or
(c) physical/chemical properties of reservoir fluids.
5. Even, if we manage to measure advancing, receding and static apparent contact angles along with the details of contact angle hysteresis – towards determining the properties of surface; whether the nature of surface roughness, chemical heterogeneity and shear hydrophobicity @ laboratory-scale and @ field-scale would more or less remain to be the same?
6. Why does apparent contact angle remain to be significantly different from (a) advancing contact angle;
(b) receding contact angle; and
(c) local contact angle?
7. How important is the ratio of drop-size to wavelength towards contact angle measurement?
8. How exactly could we get rid-off stick-slip movement of drops; and what exactly happens when the drop volume exceeds 10 micro-liters – towards contact angle measurement?