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作 者:李祖碧[1] 王加林[1] 曹秋娥[2] 徐其亨[2] 李立新[3]
机构地区:[1]云南大学成人教育学院 [2]云南大学化学系,昆明650091 [3]昆明贵金属研究所
出 处:《分析试验室》1999年第6期10-14,共5页Chinese Journal of Analysis Laboratory
摘 要:提出了在弱酸介质中钌催化高碘酸盐氧化丁基罗丹明B(BRB),以光度法测定钌。催化反应速率与催化剂浓度呈线性关系的范围为0.2~18ng/25m L,检出限为2.8×10- 12 g/m L。相对标准偏差小于14% 。催化反应对Ru(Ⅲ)、BRB、KIO4 和H3PO4 均为一级反应,表观活性能为42.12 kJm ol- 1。探讨了反应机理。本法已用于某些岩矿和冶金产品中钌的测定。RSD为1.02% ~2.29% ,回收率为98.7% ~102.0%A kinetic method is suggested for ruthenium determination by its catalytic action on oxidation of butylrhodamine B (BRB) with periodate in a weakly acid medium by spectrophotometric measurements of the reaction rate.There is a linear dependence between the rate of reaction and catalyst concentration in the range of 0 2~18ng/25mL for Ru.The detection limit is 2 80×10 -12 g/mL for Ru.The relative standard deviation for 11 replicate measurements of 0 2,5 and 15ng/25mL of Ru(Ⅲ) is 13 73%,7 35% and 2 09%,respecively.The catalytic reaction is first order for Ru(Ⅲ),BRB,KIO 4 and H 3PO 4,and the apparent activation energy of the catalytic reaction was found to be 42 12kJ mol -1 .The reaction mechanism is discussed.1000 fold excess of Ag +,400 fold Pt(Ⅳ) and Pd(Ⅱ),30 fold Au(Ⅲ) and Ir(Ⅳ) and 10 fold Os(Ⅷ) do not interfere.The method was used for the determination of nanogram amount of ruthenium in some ores and metallurgical products.The RSD( n =8) was 1 02%~2 29% and recoveries were 98 7%~102 0%
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