Effect of Chloride Ions on the Hydrolysis of Trivalent Lanthanum, Praseodymium and Lutetium in Aqueous Solutions of 2 M Ionic Strength

2005 ◽  
Vol 34 (4) ◽  
pp. 427-441 ◽  
Author(s):  
H. López-González ◽  
M. Solache-Ríos ◽  
M. Jiménez-Reyes ◽  
J. J. Ramírez-García ◽  
A. Rojas-Hernández
1994 ◽  
Vol 59 (6) ◽  
pp. 1311-1318 ◽  
Author(s):  
Ladislav Svoboda ◽  
Petr Vořechovský

The properties of cellulose chelating ion exchangers Ostsorb have been studied in the sorption of cadmium and lead from aqueous solutions. The Cd(II) and Pb(II) ions are trapped by the Ostsorb OXIN and Ostsorb DETA ion exchangers most effectively in neutral and alkaline media but at these conditions formation of stable hydrolytic products of both metals competes with the exchange equilibria. From this point of view, Ostsorb DTTA appears to be a more suitable sorbent since it traps the Pb(II) and Cd(II) ions in acidic media already. Chloride ions interfere with the sorption of the two metals by Ostsorb DTTA whereas the ionic strength adjusted by the addition of sodium perchlorate does not affect the exchange capacity of this ion exchanger.


2015 ◽  
Vol 05 (05) ◽  
pp. 161-170
Author(s):  
Miguel Angel Hernández-García ◽  
Hilario López-González ◽  
Alberto Rojas-Hernández

1969 ◽  
Vol 22 (6) ◽  
pp. 1111 ◽  
Author(s):  
AW Fordham

The hydrolysis of iron(III) has been studied by spectrophotometric methods in KaClO4, NaCl, and CaCl2 solutions all of the same ionic strength 0.15M. The measured values of the hydrolysis constants, expressed in a form which allows for association of iron with the supporting medium, were 14.5 x 10-4 in NaClO4, 8.8 x 10-4 in NaCl, and 10.9 x 10-4 in CaCl2. In addition, the extent of complex formation between iron(III) and chloride ions has been measured in perchlorate solutions of the same ionic strength 0.15M. Assuming that only chloro complexes were formed in these systems, the stability constant of FeCl2+ formation was found to be 4.0. ��� All the results obtained were sufficiently consistent with each other, within experimental error, that the inclusion of terms to account for iron-perchlorate association was unwarranted. However, if iron-perchlorate association was assumed to exist and the results were treated accordingly, the stability constant of the associated complex was estimated to be 1.8.


1986 ◽  
Vol 51 (11) ◽  
pp. 2437-2443
Author(s):  
František Kopecký ◽  
Mária Vojteková ◽  
Milan Pešák

The conventional activity of chloride ions was measured by an ion-selective electrode at 25 °C in aqueous solutions of benflurone, i.e. 5-(2-(N,N-dimethylamino)ethoxy)-7-oxo-7H-benzo(c)fluorene hydrochloride, without or with additions of KCl. These results suggest a gradual association of benflurone; the formation of a hetero-associate, (BH+)2Cl-, followed by higher associates was evaluated in the measured range up to 0.1 mol l-1.


1981 ◽  
Vol 46 (5) ◽  
pp. 1229-1236 ◽  
Author(s):  
Jan Balej ◽  
Milada Thumová

The rate of hydrolysis of S2O82- ions in acidic medium to peroxomonosulphuric acid was measured at 20 and 30 °C. The composition of the starting solution corresponded to the anolyte flowing out from an electrolyser for production of this acid or its ammonium salt at various degrees of conversion and starting molar ratios of sulphuric acid to ammonium sulphate. The measured data served to calculate the rate constants at both temperatures on the basis of the earlier proposed mechanism of the hydrolysis, and their dependence on the ionic strength was studied.


1965 ◽  
Vol 43 (1) ◽  
pp. 30-39 ◽  
Author(s):  
C. T. Bishop ◽  
M. B. Perry ◽  
F. Blank ◽  
F. P. Cooper

A group of polysaccharides, called galactomannans I, were precipitated as their insoluble copper complexes from aqueous solutions of the crude polysaccharides obtained from each of the organisms designated in the title. The five galactomannans I were homogeneous under conditions of electrophoresis and ultracentrifugation and had high positive specific rotations. The major constituent monosaccharide was D-mannose; amounts of D-galactose ranged from nil for the polysaccharide from T. rubrum to 13% for that from T. schönleinii. Methylation and hydrolysis of the five galactomannans I yielded varying amounts of the following: 2,3,5,6-tetra-O-methyl-D-galactose (not present in the products from T. rubrum), 2,3,4,6-tetra-O-methyl-D-mannose, 2,3,4-tri-O-methyl-D-mannose, 2,4,6-tri-O-methyl-D-mannose, 3,4-di-O-methyl-D-mannose, and 3,5-di-O-methyl-D-mannose. Periodate oxidation results agreed with the methylation studies. The gross structural features of each galactomannan I appear to be the same, namely, a basic chain of 1 → 6 linked α-D-mannopyranose units for approximately every 22 of which there is a 1 → 3 linked α-D-mannopyranose residue. Branch points occur along the 1 → 6 linked chain at the C2 positions of the D-mannopyranose units and once in every 45 units at the C2 position of a 1 → 6 linked D-mannofuranose residue. The D-galactose in the polysaccharides is present exclusively as non-reducing terminal furanose units; non-reducing terminal units of D-mannopyranose are also present. The variations in the identities and relative amounts of the non-reducing terminal units were the only apparent differences in the gross structural features within this group of polysaccharides.


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