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催化极谱法测定矿石中微量铼方法改进 被引量:9

THE IMPROVEMENT OF CATALYSIS POLAROGRAPHIC ANALYSIS IN DETERMINATION OF TRACE RE IN ORE
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摘要 采用2.5次微分催化极谱法,在硫酸—硫酸羟胺—硫酸钠—抗坏血酸—碲(Ⅳ)混合底液中,在国产JP3-1型极谱仪上,于起始电位-0.700伏,终止电位-1.200伏,测定矿石中微量铼。铼浓度在0—15μg/25m l可保持线性关系,且灵敏度高,重现性好,完全满足钼矿、辉钼矿中,以及其他矿物中微量铼的测定。 By the quardratic,pentad differentiation catalysis polarographic method,in the mixed base solution of sulphuric acid-hydroxylamine sulfate-sodium sulfate-ascorbic acid-Te,with the polarograph instrument Jp3-1 type made in China,start potential 0.700 V,end potential 1.200 V,the trace Re in ore is determined,which can keep the linear relationship as the Re concentration 0~15 μg/ml,sensitivity high,repeatability good,and completely meet the requirement of the determination of trace Re in Mo ore,molybdenite and other minerals.
出处 《云南地质》 2011年第2期204-207,共4页 Yunnan Geology
关键词 2.5次微分 微量铼测定 CaO烧结 催化极谱法 矿石 Quadratic Pentad Differentiation Determination of Trace Re CaO Sintering Catalysis Polarographic Method
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参考文献3

  • 1陈永乐.导数极谱法测定铼.分析化学,1974,.
  • 2杨银川.矿石中微量铼的示波极谱测定.理化检验:化学分册,1983,.
  • 3舒柏崇.铼的极谱催化氢波及其应用.分析化学,1986,:340-340.

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