Wz. Hu et al., ELECTROSTATIC ION CHROMATOGRAPHY .2. PARTITIONING BEHAVIORS OF ANALYTE CATIONS AND ANIONS, Analytical chemistry, 66(15), 1994, pp. 2514-2520
Partitioning behaviors of analyte cations and anions in ''electrostati
c ion chromatography (electrostatic IC)'' were investigated. Detectors
of ICP-AES (inductively coupled plasma atomic emission spectrometry),
UV absorption, and conductivity were connected on-line to the electro
static IC and used for the selective detection of cations, anions, and
''ion-pairing-like forms'' (both cations and anions), respectively. W
hen a mixed electrolytic aqueous solution containing cations A, C, ...
, Y, and anions B, D, ..., Z, was passed through the electrostatic IC
column, the analyte ions, which dissociated from the original salts AB
, CD, ..., and YZ, were each redistributed and forced into a new state
. This new state was termed an ion-pairing-like form because of the si
multaneous electrostatic attraction and repulsion interactions. The sa
me species of anion or cation are found in more than one ion-pairing-l
ike form; however, they occur in different volumes. What is more, each
ion-pairing-like form has a different priority of formation. Born's e
quation was used to evaluate that priority. Retention time of the ion-
pairing-like form was dependent on the species of the anion and the ch
arge of the cation. All ion-pairing-like forms can be simultaneously s
eparated with the exception of those having the same anion species as
well as the same cation charge. Ion chromatography using a strong/stro
ng positive/negative charged zwitterionic stationary phase with pure w
ater as the mobile phase was termed electrostatic ion chromatography.(
1)