E. Chibowski et al., CHANGES IN ZETA-POTENTIAL AND SURFACE FREE-ENERGY OF CALCIUM-CARBONATE DUE TO EXPOSURE TO RADIOFREQUENCY ELECTRIC-FIELD, Colloids and surfaces. A, Physicochemical and engineering aspects, 92(1-2), 1994, pp. 79-85
A calcium carbonate (Fluka; more than 99.0% pure) suspension or a thin
layer of its powder deposited on a glass slide was exposed to an r.f.
electric held (44 MHz; 60 V peak-to-peak no-load amplitude) for 5-30
min. The zeta potential of the suspension in water (natural pH, 9.9 +/
- 0.1) or in 10(-2) M NaCl (natural pH, 9.6 +/- 0.1) was then measured
electrophoretically. The surface free energy components, i.e. non-pol
ar Lifshitz-van der Waals (gamma(S)(LW)) and polar (acid-base) electro
n donor (gamma(S)(-)) and electron acceptor (gamma(S)(+)) were determi
ned by the ''thin-layer wicking technique''. It was found that a negat
ive zeta potential of CaCO3 in water measured immediately (within 2-3
min) after the exposure to the r.f. field changed in an oscillatory fa
shion depending on the exposure time. For the sample treated for 15 mi
n with the r.f. field the zeta potential decreased by 5-7 mV in relati
on to an untreated sample. Residual changes occurred also in an oscill
atory fashion during the 40 min after held removal. A similar behavior
was found for the suspension in 10(-2) M NaCl. The observed zeta pote
ntial changes were accompanied by changes in the electron donor compon
ent of the surface free energy and the appearance of a small electron
acceptor component, which resulted from the presence of hydrogen bondi
ng on the calcium carbonate surface. The r.f. held treatment led to a
decrease in gamma(S)(-) from 83 mJ m(-2) (untreated sample) to 40 mJ m
(-2) (15-min-treated sample) and 64 mJ m(-2) (25-min-treated sample) a
nd caused the appearance of gamma(S)(+) components of 1.34 and 1.77 mJ
m(-2). The observed changes in the zeta potential and the surface fre
e energy components are believed to result from the changes in the sur
face charge of calcium carbonate and the structure of the water film a
t the surface.