Exchangeability procedure

J. X. Khym, Analytical Ion-Exchange Procedures in Chemistry and Biology, Prentice-Hall, Englewood Cliffs, NJ, 1974. 

Enol ethers of 17-ketones are formed by pyrolysis of the corresponding dialkyl ketals and enol acetates are readily prepared by the exchange procedure.The latter derivatives are widely used as reactive intermediates for the introduction of substituents at C-16. 

Cyanohydrins are prepared from unsubstituted 20-ketones by the exchange procedure but not in the presence of a diluent. A 17a-hydroxyl group inhibits the exchange reaction but 20-ketones react with potassium cyanide even in the presence of Ha-bromo or 21-acetoxy substituents. 

The accumulator in the upstream is designed in such a way that the calendering process can mn steadily while splicing the tail end of a fabric with the lead end of the fabric of the next roU. The accumulator in the downstream takes care for a constant process during the exchange procedure at the winding station. 

The sizes of the voids decrease in order Cs, Rb, Na, K These differences are ascribed to the different influence of cation on the surrounding reactive species that changes the nature of alkali cation - aluminosilicate anion complexes. On the other hand, in the case that the cations are introduced in the matrix by ion exchange, (procedure b) the r3 lifetimes are approximately the same for all the cations (Table 2) and the size of cation does not have such pronounced influence. The calculated radii are shown in Table 4. 

The synthesis procedure led to a highly crystalline MCM-22 zeolite, as indicated by XRD data (Fig. 1A, a). The introduction of platinum by ion exchange procedure does not modify the crystallinity of the zeolite (Fig. 1A, b). SEM micrographs show that the sample obtained in static hydrothermal conditions is characterized by the presence of homogeneous round-shaped particles of ca. 10 pm in diameter formed by aggregation of lamellar particles [7,8], The morphology of the zeolite is not modified after platinum introduction (Fig. IB). 

The parent NH4ZSM-5 (Zeolyst, Si A 1=15) was treated with a 0.1 M Co(N03)2 at room temperature. The ion exchange procedure was repeated three times and then the precipitate was washed with water and dried at 380 K. The cobalt content corresponded to Co/Al = 0.18. We used also MgZSM-5 (Mg/Al = 0.10) obtained by the treatment of NH4ZSM-5 with Mg(N03)2 solution. Propene (MERCK 99 %), as well as carbon monoxide, and nitrogen monoxide (Linde Gas Polska 99.95%, and 99.5% resp.) were used as adsorbates. 

The template was removed by calcination in dry air at 480°C for 8 h. The calcined samples were subsequently converted to the ammonium form by an ion-exchange procedure with NH4NO3 (IN) solution at 60°C for 24 h. 

In spite of the nominal absence of Bronsted acid sites, it is possible to introduce copper species in the S-l matrix by following an ion-exchange procedure. The unit cell of the S-l can be written as follow [1] ... 

A closer inspection of the adsorption-desorption N2 isotherm at 77 K for S-l sample, before and after introducing Cu2+ ions by standard ion-exchange procedure, supported... 

The tritiated version could be prepared from tritiated formic acid which we had prepared at high specific activity (2.5 Ci mmol-1) by a metal-catalyzed hydrogen-tritium exchange procedure using T2 gas. The material can be stored either as a solid or as a solution if the latter any release of tritium by back exchange can be easily monitored by 3H NMR spectroscopy. In our experience very little exchange occurs over several weeks of storage [51]. 

Table 5.6 compares the ICP-AES results with data generated for the same sample by two other independent methods - isotope dilution spark source mass spectrometry (IDSSMS), and graphite furnace atomic absorption spectrometry (GFAAS). The IDSSMS method also uses 25-fold preconcentration of the metals and matrix separation using the ion exchange procedure, following isotope... 

Cations other than Li+ can be introduced into the film by a simple ion-exchange procedure, and this may be a simple method for obtaining multilayered structures with any cation. Organic cations, e.g., cyanine dyes, can also be introduced into the film by this procedure. Perhaps this approach for the application of highly ordered thin LB films onto the surface of electrodes could yield some new results, such an improvement in response time, as was discussed in Section 7.3.7. 

Dramatic advances in mass spectrometry and improvements in the various steps within the experimental hydrogen exchange procedures have resulted in the development of automated systems for high-throughput, high-resolution H/D exchange analysis [6, 8, 40-44]. 

Many pesticides degrade to polar products that form organic anions in a water matrix. These are sometimes missed due to the difficulty in extracting trace amounts of the ionic material from a water matrix. A recently developed anion exchange procedure for isolating acidic compounds from dilute aqueous solutions (10-12) was used for recovering the anionic material from liquid samples collected from the two pits. 

Demonstration of the feasibility and efficiency of reactive ion exchange procedures for the detoxification of carbamates. 

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