The alternation of the nature of the stationary phase due to the application of the electric field was observed in electrochromatography. [1][2][3][4][5][6][7] In electrochromatography, the retention time and peak height of a solute depended on the period from the beginning of the voltage application.2,3 The capacity factor in electrochromatography was found to depend to some degree on the value of the applied voltage. [4][5][6] The application of the electric field on the ion exchange packing supports in electrochromatography induced the release of the sample solutes from the stationary phase 5 and the variation of distribution coefficient. 6 During the application of electric voltage, the surface charges of the fluorinated-bonded silica phase altered. 7 These phenomena indicated the alternation of the nature of the stationary phase due to the application of electro voltage which was also evidenced in the dependence of the electric resistance of the column on applied voltage as was discovered in the cation exchange resin support. 4 In this article, the relationship between the electric resistance variation and the surface charges of some packing materials in electrochromatography was studied. This provides additional evidence of the alternation of the nature of the stationary phase caused by the electro voltage application.
Experimental
Apparatus, column and materialsThe same instrument for pressurized flow driven electrochromatography as described in the former reports 3,4,7,8 was used with different types of columns. A high-voltage power supply (dc ± 30 kV, type HCZE-30P, Matsusada Precision, Kusano, Shiga) was used. The expression "applied + X kV" means that +X kV is applied to the column outlet and the split injector is grounded. Fluorinated-bonded silica (type Fluofix 120E, 80421, particle diameter 5 µm, pore size 120 Å, surface area 300 m 2 /g, Neos Co., Ltd., Kobe) in the capillary column (150 µm i.d., 18.6 cm packed part, 28.6 cm total capillary length)