This is to comment on trueblood's excellent advice.
Books say that a more accurate capillarity equation for the estimation of surface tension would have to bring into account the difference between the densities of the liquid and the vapor at the top of the column ([ρ]
l-[ρ]
v), and the fact that at the top of the liquid column the surface is not flat, meaning that the radius of curvature of the meniscus should be accounted for when measuring h.
The more accurate equation with highlighted corrections would then be:
[σ] = 0.5 (rg/cos [θ])([ρ]l-[ρ]v)[h + (r cos [θ])/3]
While the typical capillarity equation generally in use:
[σ] = 0.5 rg[ρ]lh/cos [θ]
where [θ] is the angle of wetting. With a "perfectly wetting liquid" this angle is zero (cos [θ] =1); most common liquids wet glass having the angle ~zero, and the formula becomes equal to that brought by trueblood.
For example: at 20
oC, ethyl acetate (EA) considered a glass-wetting liquid, rises 4.12 cm in a capillary tube of radius 0.01294 cm. The density of EA at this temperature is 0.9005 g/cm
3.
The estimated surface tension, applying the more "accurate" formula, assuming [θ] = 0, g = 9.81 m/s
2, and [ρ]
air=0.00117 g/cm
3:
[σ] = 0.5(4.12+0.01294/3)(0.9005-0.00117)(981)(0.01294) ~ 23.54 dyne/cm
The value, as estimated by the simplified equation, would be:
[σ] = 0.5(4.12)(0.9005)(981)(0.01294) ~ 23.54 dyne/cm
Which tells us that if the liquid in hand "wets" the capillary, trueblood's advice on the measuring procedure would be applicable and the results accurate enough.