Ionic chromatography-conductivity

Water analysis parameters such as pH, electric conductivity, oxidation-reduction potential and temperature were measured in the field. Ionic chromatography, turbidimetry and ICP-OES were used for anions and metals. 

Capacitive coupling contactless conductivity detectors (C4D) which avoid contact with the solutions using high frequencies (>1 MHz) have gained popularity due to their applications in capillary electrophoresis and ionic chromatography [20,21,29,30]. These have also been coupled to flow... 

Conductivity detectors, commonly employed in ion chromatography, can be used to determine ionic materials at levels of parts per million (ppm) or parts per bUHon (ppb) in aqueous mobile phases. The infrared (ir) detector is one that may be used in either nonselective or selective detection. Its most common use has been as a detector in size-exclusion chromatography, although it is not limited to sec. The detector is limited to use in systems in which the mobile phase is transparent to the ir wavelength being monitored. It is possible to obtain complete spectra, much as in some gc-ir experiments, if the flow is not very high or can be stopped momentarily. 

Ion chromatography (IC) is a relatively new technique pioneered by Small et al.25 and which employs in a novel manner some well-established principles of ion exchange and allows electrical conductance to be used for detection and quantitative determination of ions in solution after their separation. Since electrical conductance is a property common to all ionic species in solution, a conductivity detector clearly has the potential of being a universal monitor for all ionic species. 

The conductance detector is a universal detector for ionic species and is widely used in ion chromatography (see Section 7.4). 

Ion chromatography (see Section 7.4). Conductivity cells can be coupled to ion chromatographic systems to provide a sensitive method for measuring ionic concentrations in the eluate. To achieve this end, special micro-conductivity cells have been developed of a flow-through pattern and placed in a thermostatted enclosure a typical cell may contain a volume of about 1.5 /iL and have a cell constant of approximately 15 cm-1. It is claimed15 that sensitivity is improved by use of a bipolar square-wave pulsed current which reduces polarisation and capacitance effects, and the changes in conductivity caused by the heating effect of the current (see Refs 16, 17). 

Conductance monitors can be used where the sample components are ionic and providing that the conductivity of the mobile phase is very low. They are used extensively in ion chromatography (p. 147) for the detection of inorganic anions, some inorganic cations and ionized organic acids. 

Ion exclusion chromatography, of ascorbic acid, 25 760 Ion hopping, 14 469 Ionic aggregates, 14 463—466 Ionically conducting polymers, 13 540 Ionic carbides, 4 647 Ionic compounds, rubidium, 21 822 Ionic conduction, ceramics, 5 587-589 Ionic crystals, 19 185. See also Silver halide crystals... 

A conductivity detector measures the electrical conductivity of the HPLC eluent stream and is amenable to low-level determination (ppm and ppb levels) of ionic components such as anions, metals, organic acids, and surfactants. It is the primary detection mode for ion chromatography. Manufacturers include Dionex, Alltech, Shimadzu, and Waters. 

Perhaps the most important of all electrochemical detection schemes currently in use is the electrical conductivity detector. This detector is specifically useful for ion exchange, or ion, chromatography in which the analyte is in ionic form. Such ions elute from the column and need to be detected as peaks on the recorder trace. 

The selection of the solvent is based on the retention mechanism. The retention of analytes on stationary phase material is based on the physicochemical interactions. The molecular interactions in thin-layer chromatography have been extensively discussed, and are related to the solubility of solutes in the solvent. The solubility is explained as the sum of the London dispersion (van der Waals force for non-polar molecules), repulsion, Coulombic forces (compounds form a complex by ion-ion interaction, e.g. ionic crystals dissolve in solvents with a strong conductivity), dipole-dipole interactions, inductive effects, charge-transfer interactions, covalent bonding, hydrogen bonding, and ion-dipole interactions. The steric effect should be included in the above interactions in liquid chromatographic separation. 

Whilst many functionalities may be reduced, reductive HPLC detectors are less commonly used. Another form of electrochemical detection is conductivity, which is useful when an analyte is ionic. Hence, it is often used in conjunction with ion-exchange chromatography (see Section 4.5.1.4). 

Ion chromatography (1C) is a separation technique related to HPLC. However, because it has so many aspects such as the principle of separation and detection methods, it requires special attention. The mobile phase is usually composed of an aqueous ionic medium and the stationary phase is a solid used to conduct ion exchange. Besides the detection modes based on absorbance and fluorescence, which are identical to those used in HPLC, ion chromatography also uses electrochemical methods based on the presence of ions in a solution. The applications of ion chromatography extend beyond the measurement of cations and anions that initially contributed to the success of the technique. One can measure organic or inorganic species as long as they are polar. 

In suppressed-ion chromatography, a separator column separates ions of interest, and a suppressor membrane converts eluent into a nonionic form so that analytes can be detected by their conductivity. Alternatively, nonsuppressed ion chromatography uses an ion-exchange column and low-concentration eluent. If the eluent absorbs light, indirect spectrophotometric detection is convenient and sensitive. Ion-pair chromatography utilizes an ionic surfactant in the eluent to make a reversed-phase column function as an ion-exchange column. 

K Tanaka, JS Fritz. Ion-exclusion chromatography of non-ionic substances with conductivity detection. J Chromatogr 409 271-279, 1987. 

Several electrolytic-conductivity detectors are produced (Table 3.5). The Laboratory Data Control Model 701 Conducto Monitor (Fig.3.59) may be operated in either a differential mode or an absolute mode. It provides direct readout in units of specific conductance and differences as small as 0.01% in the differential mode between the carrier and the carrier plus solute can be measured. The dynamic range of linearity is 0.01-100,000 pSl 1 /cm. The detector can function in solvents ranging from distilled water to concentrated salt solutions without the necessity of changing the cell. The volume of the cell is 2.5 pi, and the nominal cell constant is 20 cm-1. This type of detector is of use mainly in high-speed ion-exchange chromatography for the detection of ionic species. 

Because the species detected by conductivity detection are ionic, ion-exchange and ion-pair chromatography are the separation modes most often used. Both methods require mobile phases containing strong electrolytes however, the detector must detect the ionic solutes without being over-... 

---