DIFFERENTIAL-PULSE POLAROGRAPHIC-DETERMINATION OF RHODIUM(III) AND RUTHENIUM(III) IN SYNTHETIC SAMPLES AFTER PRECONCENTRATION OF THEIR QUINOLIN-8-OLATE COMPLEXES ONTO MICROCRYSTALLINE NAPHTHALENE
Rk. Dubey et al., DIFFERENTIAL-PULSE POLAROGRAPHIC-DETERMINATION OF RHODIUM(III) AND RUTHENIUM(III) IN SYNTHETIC SAMPLES AFTER PRECONCENTRATION OF THEIR QUINOLIN-8-OLATE COMPLEXES ONTO MICROCRYSTALLINE NAPHTHALENE, Microchemical journal, 58(1), 1998, pp. 117-126
Rhodium(III) and ruthenium(III) form water-insoluble quinolin-8-olate
complexes that are quantitatively retained on microcrystalline naphtha
lene in the pH ranges 5.1-6.8 and 4.0-6.5, respectively. The metal com
plex is desorbed with 10 ml of 2 M HCl and determined using a differen
tial pulse polarograph. The detection limits are 0.06 ppm for rhodium
and 1.0 ppm for ruthenium. Linearity is maintained in the concentratio
n ranges 0.25-7.50 ppm for rhodium and 2.0-60.0 ppm for ruthenium, wit
h correlation factors of 0.9997 and 0.9994 and relative standard devia
tions of 0.79 and 0.81%, respectively. The effects of various paramete
rs such as pH, volume of aqueous phase, reagent and naphthalene concen
trations, and interference of a large number of metal ions and anions
on the determination of these metals were studied in detail to optimiz
e the conditions for their trace determination in various synthetic sa
mples corresponding to real samples. The method is found to be highly
selective, fairly sensitive, simple, rapid, and economical and may be
safely applied to their determination in different complex materials s
uch as environmental samples and ores. (C) 1998 Academic Press.