The possibility of measuring in situ the interfacial tension at the mo
nomer-swollen polymer-water interface of synthetic latices is consider
ed in detail. Experimental measurements of certain liquid or vapor pha
se properties of the latex can, in principle, yield values of the desi
red interfacial tension. This technique requires the evaluation and co
mparison of the Flory-Huggins term and the Morton term of the thermody
namic expression for the chemical potential of the monomer in the late
x particle. While each term can be evaluated, it turns out that the re
lative magnitudes of the two terms are such that unrealistically high
precision is required in the experimental measurements for this techni
que to be useful for obtaining reasonably accurate interfacial tension
s. At saturated swelling conditions with highly surface-active emulsif
iers (e.g., sodium dodecyl sulfate), the interfacial tension values ob
tained have a precision of only about +/-50%. The realibility of these
approximate values degrades rapidly as one moves away from saturation
conditions, so as to render in situ experimental techniques inappropr
iate for gaining accurate knowledge about the surface energy at the la
tex particle-water interface at any monomer-polymer ratio. (C) 1994 Jo
hn Wiley & Sons, Inc.