Da. Hoagland et al., Capillary electrophoresis measurements of the free solution mobility for several model polyelectrolyte systems, MACROMOLEC, 32(19), 1999, pp. 6180-6190
The free solution electrophoretic mobilities of poly(styrenesulfonate), ss-
DNA, and duplex DNA are measured by capillary electrophoresis across a rang
e of ionic strengths and, for poly(styrenesulfonate) and ss-DNA, across a r
ange of chain lengths. The data are then compared with mobilities reported
in the literature and predicted by theory. For ionic strengths below 0.1 M,
the capillary method is more accurate and rapid than previous techniques;
it also provides a distribution of mobility values for polyelectrolyte mixt
ures. A maximum of the free solution mobility with respect to chain length
is discovered in the oligomer range for both poly(styrenesulfonate) and ss-
DNA; lowering ionic strength accentuates this unexplained phenomenon. In th
e large chain limit, where the mobility is independent of chain length, the
ionic strength dependences of mobility for all three polymers are remarkab
ly similar. These dependences can only be explained by models that incorpor
ate nonlinear electrostatic effects into the description of the counterion
cloud. The Manning model (with relaxation correction) best approximates the
dependence of mobility on ionic strength.