THE POLAROGRAPHIC DETERMINATION OF TIN IN HIGH PURITY ZINC AND ZINC DIE-CASTING ALLOYS

1947 ◽  
Vol 25b (3) ◽  
pp. 322-330 ◽  
Author(s):  
R. C. Hawkings ◽  
D. Simpson ◽  
H. G. Thode

A procedure has been developed for the determination of tin in high-purity zinc and zinc die-casting alloys present in amounts from 0.001 to 0.2%. The samples are dissolved in sulphuric acid, oxidized with hydrogen peroxide, precipitated with cupferron, redissolved and reduced, and finally the tin is determined polarographically. By this method, the tin can be determined with an accuracy of ± 2.0% when present in amounts less than 0.005%. A method is now available for the routine polarographic determination of trace amounts of copper, lead, cadmium, and tin in high-purity zinc and zinc die-casting alloys with a high degree of accuracy and precision.

1952 ◽  
Vol 6 ◽  
pp. 1217-1222 ◽  
Author(s):  
Alfreds J. Sietnieks ◽  
Erik Vasseur ◽  
I. Werner ◽  
Ernst Finsnes ◽  
Jörgine Stene Sörensen ◽  
...  

1957 ◽  
Vol 16 ◽  
pp. 194-200 ◽  
Author(s):  
J.A. Page ◽  
D.H. Simpsonb ◽  
R.P. Graham

1950 ◽  
Vol 28f (5) ◽  
pp. 128-133 ◽  
Author(s):  
B. R. Potts

A simple, rapid polarographic procedure for the determination of titanium in paint pigments has been developed, using a sulphuric acid – tartaric acid medium. The accuracy and precision of the method are satisfactory for routine testing operations. The interference of other common pigment ingredients is discussed, and a procedure suggested for the removal of copper and antimony prior to analysis.


1969 ◽  
Vol 15 (11) ◽  
pp. 1072-1078 ◽  
Author(s):  
Thomas H Steele

Abstract A semi-automated resorcinol method for the determination of inulin in plasma and urine specimens, using standard AutoAnalyzer modules, is described. Plasma and other protein-containing fluids undergo a preliminary manual protein precipitation procedure. The deproteinized specimens are processed at a rate of 50/hr, with a high degree of accuracy and precision. The superiority of the present method is largely due to the elimination of small acid-resistant pump tubes from the manifold. This is possible because reagents are premixed prior to aspiration into the system, allowing simplification of manifold design over other automated methods.


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