The simultaneous determination of nickel and zinc in secondary aluminium alloys by means of the polarograph

The Analyst ◽  
1948 ◽  
Vol 73 (872) ◽  
pp. 613 ◽  
Author(s):  
B. A. Scott
2015 ◽  
Vol 18 (2) ◽  
pp. 145-151
Author(s):  
Chau Minh Huynh ◽  
Thu Du Ly ◽  
Thach Thai Pham ◽  
Tran Thi Bao Pham ◽  
Minh Khanh Duong ◽  
...  

Conventional spectrophotometric methods for simultaneous determination of nickel, lead and zinc in forms of complexes with a reagent is not feasible due to the overlap of their absorption spectra. A multivariate calibration method was used to overcome this problem. In this study, the calibration model was constructed based on absorption spectra of 30 mixture standards in the range from 490 to 600 nm. Factors influencing experimental results such as amount of reagents, pH, and color development time were optimized. The standard calibration ranges for determination of nickel, lead and zinc were found at 0.5-5 ppm. The method was applied for determination of these ions in tap water samples at ppm level, with recoveries (and RSD) of nickel, lead and zinc were 103.3 % (3.0 %), 74.9 % (11.5 %) and 104.6 % (4.6 %), respectively.


2011 ◽  
Vol 8 (2) ◽  
pp. 587-593 ◽  
Author(s):  
Maliheh Barazandeh Tehrani ◽  
Effat Souri

A simple and sensitive derivative spectrophotometric method for simultaneous determination of nickel and copper using 6-(2- naphthyl)-2,3-dihydro-1,2,4-triazine-3-thione (NDTT) as a selective analytical reagent was developed. The complexes of metal ions with NDTT were formed immediately in basic media and extracted with chloroform. The zero-crossing measurement technique was found suitable for the direct measurement of the third-derivative value of Ni-NDTT and Cu-NDTT at 501 and 472 nm respectively. Beer’s law is obeyed in the concentration range 1-30 μg/mL for both cations with different ratios. The limit of detection was 0.26 μg/mL and 0.13 μg/mL for copper and nickel respectively. The within day and between day variations showed coefficient of variation (CV%) values less than 2.80 and 2.97 for copper and nickel respectively. The error of the determination method did not exceed 6.50%. Analysis of alloy sample showed that this method can be successfully used for simultaneous determination of Cu and Ni in real samples.


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