摘要
The paper presents a new method of determining Ge in gold alloys by potassium iodate potentiometric titration rather than by traditional distillation separation. The influences of conditions such as the reduction acidity, dosage of sodium hypophosphite and reduction time on the determination of Ge were studied. Comparison was made between the influences of end-point indication for potential method and starch method on accruracy and precision of the analysed results, stability and sensitivity of end-point, selectivity of method and so on. The possibility of reaction in an electrochemical way was discussed. Ge in the alloys such as AuGe 12 , AuGeNi 12 2 , AuAgGe 18.8 12.5 and AuAgGeNi 43.8 6 0.2 was measured, respectively, with the relative standard deviation of 0.10%~0.31% and the recoveries of added standard Ge in sample of 99.40%~100.40% when the reduction acidity was 0.40~0.80 mol/L HCl and 3.3 mol/L H 3 PO 4, 15 g sodium hypophosphite and reduction time 40 min. The new method presented is high accuracy and precision in results, good stability and sensibility in end point, easy operation and strong selectivity of determination. When it is applied to analyse actual samples, satisfactory results are achieved.
The paper presents a new method of determining Ge in gold alloys by potassium iodate potentiometric titration rather than by traditional distillation separation. The influences of conditions such as the reduction acidity, dosage of sodium hypophosphite and reduction time on the determination of Ge were studied. Comparison was made between the influences of end-point indication for potential method and starch method on accruracy and precision of the analysed results, stability and sensitivity of end-point, selectivity of method and so on. The possibility of reaction in an electrochemical way was discussed. Ge in the alloys such as AuGe:2, AuGeNi12-2, AuAgGel8.8-12.5 and AuAgGeNi43.8-6.0.2 was measured, respectively, with the relative standard deviation of 0.10%-0.31% and the recoveries of added standard Ge in sample of 99.40%-100.40% when the reduction acidity was 0.40-0.80 mol/L HC1 and 3.3 mol/L H3PO4, 15 g sodium hypophosphite and reduction time 40 min. The new method presented is high accuracy and precision in results, good stability and sensibility in end-point, easy operation and strong selectivity of determination. When it is applied to analyse actual samples, satisfactory results are achieved.
出处
《贵金属》
CAS
CSCD
北大核心
2012年第A01期298-304,共7页
Precious Metals
基金
The National High Technology Research and Development Program of China(2012AA063203,2012AA063207)
Research Foundation of Kunming Institute of Precious Metals(GY08RD27)