Abstract

The separation was carried out at 90°C. The developing solution used was 0.05, 3M hydrochloric acid and 0.28% ammonia water. Initially, formation of metal complex was tried as a means to separate the metal ions. Filter papers impregnated with 1% dimethylglyoxime, 1% 8-quinolinol, saturated rebeanic acid, 0.1% p-dimethylaminobenzylidenrhodanine, 0.05% benzidine, 0.2% bismuthiol II, 0.1% p-nitrosodimethylaniline, 0.1% 1-(2-pyridilazo)-2-napthol, 1% sodium diethyldithiocarbonate and 0.1 % ascorbic acid solution were used. Metal ions were separated by combining these papers and the developing solutions. Metal ions were separated into two groups, further separation into individual metal ions was not possible. Individual metal ion separation was achieved based on the solubilities of metal sulfides and the formation of a metal complex. Six metal ions, Au(III), Ir(IV), Pd(II), Pt(IV), Rh (III) and Ru(III), were separated. The time necessary for the separation was about 1h. The metal ions were detected from the colors of either their sulfide or metal complex. Separable ranges were Au(III); 0.251.0μg, Ir(IV);0.21.5μg, Pd(II); 0.31.8μg, Pt(IV); 0.62.2μg, Rh(III); 0.451.2μg and Ru (III); 0.30.7 μg. The lower value for each element (ion) shows the detection limit.

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