Comparative studies on the isothermal characteristics of proteins adsorbed under batch equilibrium conditions to ion-exchange, immobilised metal ion affinity and dye affinity matrices with different ionic strength and temperature conditions

1997 ◽  
Vol 763 (1-2) ◽  
pp. 71-90 ◽  
Author(s):  
Gerard M.S. Finette ◽  
Qui-Ming Mao ◽  
Milton T.W. Hearn
2010 ◽  
Vol 25 (2) ◽  
pp. 178-184 ◽  
Author(s):  
Ola Sundman ◽  
Per Persson ◽  
Lars-Olof Öhman

Abstract A compilation of the applied experimental conditions when studying metal ion adsorption onto kraft fibres, and the resulting conclusion, revealed that the ionic strength conditions used during the experiments were an important dividing factor. At low ionic strengths, the conclusion has regularly been that the Donnan ion-exchange model could correctly predict the adsorption while, at higher ionic strengths, it has often been concluded that the formation of specific metal-ion fibre complexes must be assumed. To study this apparent influence from the presence of monovalent sodium ions, Cu K-edge EXAFS spectra of Cu2+ ions adsorbed to kraft fibres were collected in media of “0” to 100 mM NaCl. Combined with previous data, these measurements confirmed that at very low ionic strength, the importance of specific interactions between the chemically modified cellulose fibres and the Cu(II) ions significantly decreased. For a detailed description of the adsorption phenomenon, both types of interactions must be considered simultaneously. For most technical and engineering applications, however, the Donnan model can be used at low ionic strength conditions, i.e. I ≲ 10 mM. At higher ionic strengths, though, the inclusion of specific complexes in the model is necessary for correctly describing the adsorption of di- and trivalent cations with strong complex forming properties.


1987 ◽  
Vol 65 (5) ◽  
pp. 1133-1138 ◽  
Author(s):  
Robert D. Guy ◽  
Sarath Namaratne

The properties of mercury-coated glassy carbon electrodes coated with a thin membrane of Nation 117 were studied to evaluate the potential analytical applications in metal ion analysis. The Nation membrane was found to contain two types of binding sites — a strong site that bound metal ions in a nonelectroactive form and cation exchange sites that were useful for preconcentrations prior to differential pulse voltammetry. The exchange constants for the weak sites ranged from 0.413 for copper to 12.5 for methyl viologen. The differential pulse currents were increased by a factor of 75 to 100 and a linear calibration curve was observed from about 25 n M to 1000 n M for copper, lead, cadmium, and zinc. The ion exchange reaction is very sensitive to ionic strength and significant enrichments occur only in solutions of ionic strength below 0.10. The Nafion-coated glassy carbon electrode in a flow cell can be used to determine the free copper ion concentration in samples by a combination of ion exchange and differential pulse voltammetry. The flow-through system required about 15 mL of sample solution and an analysis time of about 10 min. The ion exchange measurement gave a linear calibration from 40 n M to 10 μ M for free copper.


2001 ◽  
Vol 79 (4) ◽  
pp. 370-376 ◽  
Author(s):  
Catherine Morlay ◽  
Yolande Mouginot ◽  
Monique Cromer ◽  
Olivier Vittori

The possible removal of copper(II), nickel(II), or lead(II) by an insoluble crosslinked poly(acrylic acid) was investigated in dilute aqueous solution. The binding properties of the polymer were examined at pH = 6.0 or 4.0 with an ionic strength of the medium µ = 0.1 or 1.0 M (NaNO3) using differential pulse polarography as an investigation means. The highest complexing capacity of the polyacid was obtained with lead(II) at pH = 6.0 with µ = 0.1 M, 4.8 mmol Pb(II)/g polymer. The conditional stability constants of the complex species formed were determined using the method proposed by Ruzic assuming that only the 1:1 complex species was formed; for lead(II) at pH = 6.0 and µ = 0.1 M, log K' = 5.3 ± 0.2. It appeared that the binding properties of the polymer increased, depending on the metal ion, in the following order: Ni(II) < Cu(II) < Pb(II). The complexing capacity and log K' values decreased with the pH or with an increase of the ionic strength. These results were in agreement with the conclusions of our previous studies of the hydrosoluble linear analogues. Finally, with the insoluble polymer, the log K' values were comparable to those previously obtained with the linear analogue whereas the complexing capacity values expressed in mmol g-1 were slightly lower.Key words: insoluble crosslinked poly(acrylic acid), copper(II), nickel(II), and lead(II) complexation.


CrystEngComm ◽  
2014 ◽  
Vol 16 (40) ◽  
pp. 9520-9527 ◽  
Author(s):  
Xiao-Tong Li ◽  
Jing Li ◽  
Meng Li ◽  
Ying-Ying Liu ◽  
Shu-Yan Song ◽  
...  

1971 ◽  
Vol 24 (10) ◽  
pp. 1979 ◽  
Author(s):  
SD Hamann

A theoretical model has been developed to describe the thermal regeneration of ion-exchange resins in the Sirotherm process1-10 for desalting water. It assumes that the thermal effect is primarily due to the large increase that occurs in the ionization of water when the temperature is raised. The hydrogen and hydroxyl ions compete with salt for exchange sites in the resins and for that reason water, itself, acts as a regenerating acid and base. ��� Calculations have been made of the equilibrium conditions, column behaviour, and titration behaviour of mixtures of weak-acid and weak-base resins with aqueous solutions of 1 : 1 and 2 : 2 electrolytes, assuming the systems to obey Donnan's equilibrium relationship. There is satisfactory agreement between the calculated and observed effects of both temperature and pressure.


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