H. Ino et al., ELECTRICAL DEMULSIFICATION OF SUBMICRON W O EMULSION IN LIQUID SURFACTANT MEMBRANE PROCESSES/, Kagaku kogaku ronbunshu, 20(3), 1994, pp. 423-430
In the ordinary high-voltage A.C. electric demulsification of W/0 emul
sion for liquid surfactant membranes, the breaking of the submicron dr
oplets has been reported to be difficult. In this work, by making the
distance between the electrodes short in an A.C. electric demulsifier
the submicron droplets were successfully broken. In the experiments, t
he oil phase was kerosene with Span 80 as the surfactant, and the inne
r aqueous phase was NaCl solution for the non-extraction system and H2
SO4 solution for the extraction system. The original W/0 emulsion, whi
ch was made with a disperser, was demulsified by an ordinary A.C. elec
tric demulsifier. The oil phase containing unbroken submicron droplets
was used as the sample emulsion. For the extraction system, W/O emuls
ion which experienced the extraction of Cu was used as the original em
ulsion. It was found experimentally that the submicron emulsion can be
demulsified by making the distance between the electrodes as short as
10 mm. The effects of water concentration C[mol.m-3], surfactant volu
me fraction Cs [-], electrical potential E[V.m-1] and temperature T[K]
on the demulsification rate, dC/dtheta, was correlated by the experim
ental equation. dC/dtheta = -k.E.Cs-1,8.C3.exp (-E0.R-1.T-1) Where the
ta[s] is time, R[J.mol-1.K-1] is gas constant, E0[J.mol-1] is apparent
activation energy and k[m7.mol-2.V-1.s-1] is constant; E0 = 43.0 x 10
(3), k = 1.54 x 10(-8), for the non-extraction system and E0 = 53.9 x
10(3), k = 4.4 x 10(-6) for the extraction system.