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活化分析分离的新原理——X 痕量镓的亚化学计量测定

A new principle of activation-analysis separations-X Substoichiometric determination of traces of gallium.

作者信息

Zeman A, Růzicka J, Kuvik V

机构信息

Department of Nuclear Chemistry, Faculty of Technical and Nuclear Physics, Prague 1 Brehová 7, Czechoslovakia.

出版信息

Talanta. 1966 Feb;13(2):271-5. doi: 10.1016/0039-9140(66)80034-6.

Abstract

A rapid method for the substoichiometric determination of gallium by neutron-activation analysis has been developed. After irradiation and dissolution of the test sample, gallium carrier is added and two preliminary separation steps are performed: the extraction into chloroform of cupferrates from 7N sulphuric acid and of diethyldithiocarbamates from 2-3N sulphuric acid. The pH of the remaining aqueous phase is then adjusted to 5.5, the solution extracted with a substoichiometric amount of 8-hydroxyquinoline in chloroform and the activity of the gallium hydroxyquinolate extract measured. A simultaneously irradiated gallium standard is treated in exactly the same way. From the activities of these two substoichiometric extracts the amount of gallium originally present in the test sample can be calculated. The method has been applied to the determination of 10(-6) to 10(-3)% of gallium in metallic aluminium and transistor-grade silicon.

摘要

已开发出一种通过中子活化分析进行亚化学计量测定镓的快速方法。测试样品经过辐照和溶解后,加入镓载体并进行两个初步分离步骤:从7N硫酸中萃取铜铁试剂至氯仿中,以及从2 - 3N硫酸中萃取二乙基二硫代氨基甲酸盐至氯仿中。然后将剩余水相的pH值调至5.5,用亚化学计量的8 - 羟基喹啉氯仿溶液萃取该溶液,并测量羟基喹啉镓萃取物的活性。同时辐照的镓标准品以完全相同的方式处理。根据这两种亚化学计量萃取物的活性,可以计算出测试样品中最初存在的镓含量。该方法已应用于测定金属铝和晶体管级硅中10^(-6)至10^(-3)%的镓。

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