文摘
A voltammetric ion-selective electrode based on thefacilitated transfer of Li+ by dibenzyl-14-crown-4 at theo-nitrophenyl phenyl ether/water interface was applied tothe amperometric detector in a FIA system for Li+ with acation-exchange column. The current response was stablydetected by pulse amperometry in which voltage pulsesof short duration (50 ms) were applied at the interval of2 s. With this FIA system, 0.2-2.0 mM Li+ in aqueoussolution could be determined even in the presence of120-160 mM Na+, the detection limit being 0.15 mM.A test using artificial serum demonstrated the practicalapplicability of this system.