Determination of the ion exchange capacity of solid ion exchangers by difference weighting

1976 ◽  
Vol 48 (14) ◽  
pp. 2279-2280 ◽  
Author(s):  
Kurt. Bunzl ◽  
Bruno. Sansoni
1992 ◽  
Vol 57 (9) ◽  
pp. 1905-1914
Author(s):  
Miroslav Bleha ◽  
Věra Šumberová

The equilibrium sorption of uni-univalent electrolytes (NaCl, KCl) in heterogeneous cation exchange membranes with various contents of the ion exchange component and in ion exchange membranes Ralex was investigated. Using experimental data which express the concentration dependence of equilibrium sorption, validity of the Donnan relation for the systems under investigation was tested and values of the Glueckauf inhomogeneity factor for Ralex membranes were determined. Determination of the equilibrium sorption allows the effect of the total content of internal water and of the ion-exchange capacity on the distribution coefficients of the electrolyte to be determined.


2014 ◽  
Vol 39 (10) ◽  
pp. 5054-5062 ◽  
Author(s):  
F. Karas ◽  
J. Hnát ◽  
M. Paidar ◽  
J. Schauer ◽  
K. Bouzek

1996 ◽  
Vol 14 (1) ◽  
pp. 5-23 ◽  
Author(s):  
Zbigniew Hubicki ◽  
Halina Hubicka ◽  
Bozena Lodyga

The applicability of selective ion exchangers for the removal of palladium(II) from solutions of copper(II), nickel(II), aluminium(III) salts, hydrochloric acid, a mixture of hydrochloric and nitric acids as well as a mixture of hydrochloric acid and ammonium chloride has been studied by frontal analysis. The best results were obtained in the purification of copper(II) and nickel(II) salts on Chelite S with functional thiol groups, Duolite ES-346 with functional amidoxime groups and Lewatit TP-214 with functional thiourea groups. A decrease of palladium(II) content below 5 × 10−5% was obtained in the process of purification of macroquantities of these salts. In addition, these ion exchangers possess a considerable ion-exchange capacity (e.g. 3.18 mequiv. Pd/g for Lewatit TP-214) and a high resistance to mineral acids.


2009 ◽  
Vol 19 (01n02) ◽  
pp. 1-8 ◽  
Author(s):  
SUREERAT THOMYASIRIGUL ◽  
HITOSHI FUKUDA ◽  
JUN HASEGAWA ◽  
YOSHIYUKI OGURI

Concerning the PIXE analysis of Cr ( VI ) in water using ion-exchange filters, the limit of detection (LOD) and the influence of matrix anions were investigated. In order to look for the experimental condition for obtaining the minimum LOD, we measured the Cr - K α X-ray counts and background counts under the K α X-ray peak as a function of the incident proton energy and the thickness of the Mylar absorber foil in front of the detector. To investigate the interference by coexisting anions, each of PO 43-, SO 42-, NO 3-, Cl -, and F - ions and Cr ( VI ) ions were mixed in aqueous solutions and adsorbed on DE81-DEAE cellulose paper, a weakly basic anion exchanger with diethylaminoethyl functional groups. Then the filter samples were measured by PIXE using 2.5 MeV proton beams. We obtained a LOD of 0.16 µg or 8 ppb for 20 mL samples at a proton energy of 2.5 MeV and a Mylar film thickness of 50 or 100 µm. The experimental results on the mixed solutions indicated that NO 3-, Cl -, and F - as coexisting ions didn't interfere significantly with determination of a 50 µ g / L Cr ( VI ) concentration for 40 mL total solution volume, despite the total amount of anions was about 90% of ion exchange capacity of a filter. On the other hand, slight interferences by PO 43- ions were observed. However, under the same condition, we found that if the total amount of SO 42- ions was higher than 20% of ion exchange capacity, they induced significant interferences in determining Cr ( VI ).


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