Ionic exchange

The formation of more replaced compounds in studied conditions is not have place. Maximal yield on surface polyurethane foam of salts is observed by pH 2-6. By pH<2 the equilibrium ionic exchanges was displaced left and by pH<0,5 the sorbent practical completely was regenerated. It was studied the influence of the weight of sorbent, the nature of cations of light alkali and alkali earth metals and any other factors on the coefficient concentration ofM(I). 

The (I)-(III)-samples sorption ability investigation for cationic dyes microamounts has shown that for DG the maximum rate of extraction is within 70-90 % at pH 3. The isotherm of S-type proves the physical character of solution process and a seeming ionic exchange. Maximal rate of F extraction for all samples was 40-60 % at pH 8 due to electrostatic forces. The anionic dyes have more significant affinity to surface researching Al Oj-samples comparatively with cationic. The forms of obtained soi ption isotherms atpH have mixed character of H,F-type chemosorption mechanism of fonuation of a primary monolayer with the further bilayers formation due to H-bonds and hydrophobic interactions. The different values of pH p for sorbents and dyes confirm their multifunctional character and distinctions in the acid-base properties of adsoi ption centers. 

Phospholipids. For the removal of ionic contaminants from raw zwitterionic phospholipids, most lipids were purified twice by mixed-bed ionic exchange (Amberlite AB-2) of methanolic solutions. (About Ig of lipid in lOmL of MeOH). With both runs the first ImL of the eluate was discarded. The main fraction of the solution was evaporated at 40°C under dry N2 and recryst three times from n-pentane. The resulting white powder was dried for about 4h at 50° under reduced pressure and stored at 3°. Some samples were purified by mixed-bed ion exchange of aqueous suspensions of the crystal/liquid crystal phase. [Kaatze et al. J Phys Chem 89 2565 7955.]... 

All sequential treatment steps must be indicated for the metal compound categories reported even if the treatment method does not affect the particular metal. For example, ionic exchange must be reported as a treatment method for lead, zinc, chromium, and selenium compounds, oven though the method affects only the selenium compound. 

The first attempts employing two Cjg columns showed that the selectivity was not high enough, although this improved when the first column was substituted by a 5 p.m GFF n internal surface rcversed-phase material. This is known as a restricted-access-material (RAM) column which, since it restricts some compounds because of their size and includes rcversed-phase interaction and ionic exchange, is very useful for analysing herbicides in samples with high contents of humic and fulvic acids (54). 

Surface ions are thus expected to substantially contribute to the polarization force at low frequencies. Also, one expects different ions to have different solvation properties and mobility. These phenomena can be explored by SPFM. They are important in surface reactions, ionic exchange processes between surface and bulk ions, rock weathering, ion sequestration, and other enviromnental problems. 

Recently, a series of chiral diphosphines (S. -Me-Duphos, (S. -chiraphos, (R,R)-diop and (+)-Norphos were grafted after an ionic exchange onto Al-MCM-41 134 complexes of the form [Rh(cod)(diphosphine)]+ were tested for the hydrogenation of dimethylitaconate. The supported complex with (S,S)-methyl-Duphos reached an activity for the formation of dimethyl ( -methyl-succinate as high as TON = 4000 with an ee close to 92%. Both (R,R)-diop and (,S S )-chiraphos give lower enantioselectivities (ee = 34% and 47% respectively). With (+)-Norphos, dimethyl-([Pg.457]

In summary, the Zn-Al and Zn-Ga based-hydrotalcites were found as very effective supports for docking a Rh(TPPTS)3Cl complex. The process was carried out via ionic exchange and occurred without any damage of die support structure or of the complex. The resulted catalysts were found to catalyze the cyclization of acetylenic carboxylic acids to the corresponding 5-membered ring heterocycles in good to excellent yields. The basic properties of the support also allow a clean and selective reaction of unsubstituted acetylenic carboxylic acids. 

In this work we modified an HZSM-5 zeolite through different dealumination treatments and partial ionic exchange with Cs+ in an attempt to modulating the zeolite acidity and thus to improving its behavior for the MDA reaction. 

Fry, C.H., D.P. Harding, and J.P. Mounsey. 1987. The effects of cyanide on intracellular ionic exchange in ferret and rat ventricular myocardium. Proc. Roy. Soc. London 230B 53-75. 

In reaction (b) an ionic exchange and solubilization of the aluminum species takes place. In reaction (c) only the solubilization of neutral aluminum species takes place. If the chemical treatment with acid in the two-step process also involves the solubilization of framework aluminum, reaction (a) takes place. 

In fact, adsorption of Ag+ can be successfully performed by an ionic exchange mechanism for pH < 5. A negatively charged PdO surface is able to adsorb Ag+ in this acidic medium. Such a solution was impregnated onto q -A1203 and results of the catalytic tests are presented in Section 13.4.3. 

Munoz and Fudington (1974, 1977) experimentally measured the ionic exchange reaction... 

The implications of diffusion kinetics for ionic exchange geothermometry have been discussed in detail by Lasaga (1983). 

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