Useful Ion-Exchange Capacity

It has been seen that this resin has also some important advantages over the other resins in the literature like high total ion exchange capacity, easy synthesis, lower cost, simple regeneration. Furthermore, very good sepai ations were obtained using a concentration gradient of elution. In these elutions, very low concentrations of sodium trimetaphosphate were used. As a result, the resin synthesized can be used as an adsorbent for the effective removal of Pb, Cd, Co, Cu, Fe, Ni, Zn and Cr from aqueous solutions. 

Films of the copolymers are, as with Nafion, saponified and used for permselective membranes. They have a much higher tensile strength than the Du Pont material and are also claimed to have a higher ion exchange capacity. 

In large power plants, precoat filters are traditionally used only when freshwater condenser cooling is employed because brine or seawater condenser leaks would quickly overwhelm the limited ion-exchange capacity available. They also are commonly used for continuous filtering of suspended corrosion products under variable power load conditions and when frequent boiler startups are necessary. 

It may be noted that the ion exchange capacity is directly connected with the Al-content (each Al provides one negative charge). The zeolite used in detergent formulations (over 10 t/a) is NaA with Si/Al = 1, so with maximum exchange abi ity. 

DRIFT spectroscopy was used to determine Av0h shifts, induced by adsorption of N2 and hexane for zeolite H-ZSM-5 (ZSM-a and ZSM-b, Si/Al=15.5 and 26), H-mordenite (Mor-a and Mor-b, Si/AI— 6.8 and 10) and H-Y (Y-a and Y-b, Si/Al=2.5 and 10.4) samples. Catalysts were activated in 02 flow at 773 K in situ in the DRIFTS cell and contacted than with N2 at pressures up to 9 bar at 298 K or with 6.1% hexane/He mixture at 553 K, i.e., under reaction conditions. Catalytic activities of the solids were measured in a flow-through microreactor and kapp was obtained as slope of -ln(l-X0) vs. W/F plots. The concentration of Bronsted acid sites was determined by measuring the NH4+ ion-exchange capacity of the zeolite. The site specific apparent rate constant, TOFBapp, was obtained as the ratio of kapp and the concentration of Bronsted acid sites. 

Standard cations used for measuring cation exchange capacity are Na+, NHJ, and Ba2+. NH is often used but it may form inner-sphere complexes with 2 1 layer clays and may substitute for cations in easily weathered primary soil minerals. In other words, one has to adhere to detailed operational laboratory procedures these need to be known to interpret the data and it is difficult to come up with an operationally determined "ion exchange capacity" that can readily be conceptualized unequivocally. 

A further calcination of the clay above 500°C induces a dehydroxylation of the solid and results in a stabilization of the porous network. However, by this point, the samples have lost their ion exchange capacity. This can be restored using 4 10 M solution of at 80°C, as described by Vaughan (3 ). Ce can then be introduced by ion exchange from a CeCl solution. 

Conductivity detector is the most common and useful detector in ion exchange chromatography. However UV and other detectors can also be useful [10]. Conductivity detection gives excellent sensitivity when the conductance of the eluted solute ion is measured in an eluent of low background conductance. Therefore when conductivity detection is used dilute eluents should be preferred and in order for such eluents, to act as effective competing ions, the ion exchange capacity of the column should be low [1]. 

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