Direct potentiometric titration of chloride and fluoride ions in reversed micelles of an ethoxylated surfactant

2000 ◽  
Vol 366 (1) ◽  
pp. 59-63
Author(s):  
A. I. Bulavchenko ◽  
E. K. Batishcheva ◽  
T. Yu. Podlipskaya ◽  
V. G. Torgov
1974 ◽  
Vol 57 (5) ◽  
pp. 1209-1216
Author(s):  
Wallace S Brammell

Abstract The official final action potentiometric titration method for sodium chloride in canned vegetable products was modified to provide a general quantitative method for foods. The product is dispersed with water and acidified, and soluble chlorides are titrated potentiometrically with silver nitrate. The method is applicable to levels of ≥0.03% sodium chloride. As in all methods involving precipitation of chlorides with silver nitrate, bromide and iodide interfere but not significantly at the levels found in most foods. Interference by protein, amino acids, and phosphate, hydroxyl, carbonate, sulfate, and fluoride ions is prevented by acidifying the sample. In the collaborative study, 10 collaborators successfully analyzed 12 different foods (beef broth, soy sauce, salted whole eggs, margarine, prepared mustard, baby food (carrots), bread, TV dinner, parmesan cheese, canned salmon, ham, and peanut butter), obtaining coefficients of variation ranging from 0.49 to 5.99%, an indication of the precision of the method. Potentiometric titration of chloride in ashed and nonashed samples gave close agreement for sodium chloride content, showing that protein and other organic matter present do not interfere, that ashing is not necessary, and that dispersion or blending with water is adequate for sample preparation. With the proposed method, the sodium chloride content of a food sample can be determined with precision and accuracy in 2—6 min. The method has been adopted as interim official first action.


1979 ◽  
Vol 44 (9) ◽  
pp. 2828-2831 ◽  
Author(s):  
Zlata Papoušková ◽  
Vlasta Fialová ◽  
Václav Chvalovský

The relative basicity of fifteen methylethoxysilylalkylamines of the type (CH3)3-m(C2H5O)m.Si(CH2)nNH2 in acetone has been studied by potentiometric titration. For n 1 the basicity increases with increasing m, which is likely due to increasing electronic interaction of the oxygen of acetone with the silicon of silylalkylamines. The basicity of silylmethylamines (n = 1) changes nonsystematically, probably as a consequence of the competing action of opposite effects.


1980 ◽  
Vol 45 (3) ◽  
pp. 910-913 ◽  
Author(s):  
Viera Knoppová ◽  
Anton Beňo ◽  
Jaroslav Kováč

Furancarboxylic acids were prepared by oxidation with Ag2O of the corresponding 5-(X-phenoxy)-2-furaldehydes (X = 4-OCH3, 4-SCH3, 3-NHCOCH3, 4-Cl, 4-Br, 4-COOC2H5, 3-NO2, and 4-NO2. The appearing pKa values of the synthesized acids were determined by potentiometric titration. The transfer effect of the substituents through the oxygen bridge is discussed and the transfer coefficient is compared with π' values of other linking groups in the furan series.


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