Mw. Martin, Selectivity of some ion chromatography stationary phases for small anions in solvent-water mixtures with hydroxide, MICROCHEM J, 62(1), 1999, pp. 203-222
The selectivity of two hydroxide-selective ion chromatography stationary ph
ases was examined with varying solvent composition. The solvents acetonitri
le 2-propanol and dimethylsulfoxide were found to diminish retention of the
se anions. However, retention times were found to increase for small anions
with increasing methanol composition. For somewhat larger anions such as p
erchlorate and tetrafluoroborate, moderately decreasing or stable retention
times were observed with increasing methanol content. The loss of retentio
n is attributed to hydroxide form resins preferentially imbibing water from
the solution phase, effectively increasing thr elution strength of hydroxi
de because of its greater hydration energy. In methanol-water mixtures to 4
0%, these types of anion exchangers are known to swell to nearly the same e
xtent (volume) as in water. Thus, hydration energy differences between hydr
oxide and these anions may not be as pronounced relative to weaker solvatio
n in methanol. Run time for common inorganic anions on a high-capacity anio
n-exchange column can be reduced from 30 to 10 min through the use of aceto
nitrile. In addition, as the acetonitrile content is increased, retention r
eversals such as bromide-nitrate and chloride-nitrite occur. Four divalent
species (sulfite, maleate, sulfate, fumarate) that are not separated on Dio
nex IonPac AS11 with hydroxide can be separated on the same column easily i
n 50% methanol. (C) 1999 Academic Press.