Green Chromatographic Techniques: Separation and by Karine Faure, Nazim Mekaoui, Alain Berthod (auth.), Dr.

By Karine Faure, Nazim Mekaoui, Alain Berthod (auth.), Dr. Inamuddin, Ali Mohammad (eds.)

This publication offers a unified outlook on counter-current, ion dimension exclusion, supercritical fluids, high-performance skinny layers, and fuel and dimension exclusion chromatographic strategies used for the separation and purification of natural and inorganic analytes. It additionally describes a couple of eco-friendly innovations, eco-friendly pattern guidance equipment and optimization of solvent intake within the chromatographic research of natural and inorganic analytes. This e-book bargains a worthwhile source not just for newbies, but additionally for more matured chromatographers, conveying a deeper figuring out of eco-friendly chromatographic thoughts, eco-friendly solvents and instruction methods.

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Extra resources for Green Chromatographic Techniques: Separation and Purification of Organic and Inorganic Analytes

Example text

Hydrated ions of calcium chloride 32 M. Tsyurupa et al. which, in reversed experiment, move faster than acid ions depart the zone of mixed solution thus liberating a corresponding space in this zone. In exclusion chromatography an additional volume of water does not fill thus liberated space. Instead of this, the zone of hydrochloric acid, that is located behind the zone of calcium chloride, gets narrower thus leading to a definite increase in the concentration of the acid. Similarly, in direct experiment, CaCl2 which passes through large pores with higher velocity than HCl moving slower through both large and small pores, gets rid of the acid and concentrates, as well.

5 mm in diameter were slurry packed in glass columns, mostly of 30 mL or 44 mL in volume (about 1 cm in diameter). In order to avoid tailing of chromatographic zones due to convective fluxes of a more dense (compared to water) solution of electrolytes, the latter was percolated through the column from its bottom upwards till the equilibration of the column with the feed solution completed. This experiment was called direct one. Afterwards, electrolytes were displaced from the column in opposite direction by the flow of pure water.

In both cases, the acids resided in the column longer than the salts. In 1958 in a theoretical study on the activity coefficients of electrolytes in the anion exchange resin phase (Dowex 1 × 10), Nelson and Kraus (1958) arrived at the conclusion that the separation of HCl from corresponding salts occurs, probably, due to a low activity of HCl in the phase of the anion exchanger. 5 bed volumes if the acid was dissolved in 5 N LiCl, while the acid retention rises to 8 bed volumes when the salt concentration increases to 16 N.

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