Ion exchange substances

Solubility - The ion-exchange substance must be insoluble under normal conditions of use. Most ion-exchange resins in current use are high molecular weight... 

To bind dietary calcium in the gut sodium cellulose phosphate (Calcisorb) is an oral ion exchange substance with a particular affinity for calcium. Bound calcium is eliminated in the faeces. It is used particularly for patients who overabsorb dietary calcium and who develop hypercalciuria and renal stones. 

Figure 7.7. Ion exchanger substances used for ISEs with liquid membrane, a Dialkylphosphate. b Nickel phenanthroline complex, c Crystal violet...

The third technique, proposed by Schlapp (512) in 1925, depends not upon precipitation of these hormonal substances, but also on selective adsorption and elution. Potts and Gallagher (477) reviewed both the methods and the adsorbants, which latter are ion-exchange substances to a greater or lesser degree, and which retain vasopressin more strongly... 

Sephadex A trade name for an insoluble hydrophilic substance prepared by cross-linking dextran, and used in gel filtration. It can also be linked to acidic or basic groups for ion exchange or to alkanes for the chromatography of lipophilic compounds. 

For very small quantities, ion exchange processes may be utilised (p. 55) even with water-soluble neutral substances. 

Ion-exchange methods are based essentially on a reversible exchange of ions between an external liquid phase and an ionic solid phase. The solid phase consists of a polymeric matrix, insoluble, but permeable, which contains fixed charge groups and mobile counter ions of opposite charge. These counter ions can be exchanged for other ions in the external liquid phase. Enrichment of one or several of the components is obtained if selective exchange forces are operative. The method is limited to substances at least partially in ionized form. 

The resuspended and formulated Fraction II precipitate normally contains some aggregated IgG and trace substances that can cause hypotensive reactions in patients, such as the enzyme prekail ikrein activator (186). These features restrict this type of product to intramuscular adininistration. Further processing is required if products suitable for intravenous adininistration are required. Processes used for this purpose include treatment at pH 4 with the enzyme pepsin [9001-75-6] being added if necessary (131,184), or further purification by ion-exchange chromatography (44). These and other methods have been fiiUy reviewed (45,185,187,188). Intravenous immunoglobulin products are usually suppHed in the freeze-dried state but a product stable in the solution state is also available (189). 

Membranes and Osmosis. Membranes based on PEI can be used for the dehydration of organic solvents such as 2-propanol, methyl ethyl ketone, and toluene (451), and for concentrating seawater (452—454). On exposure to ultrasound waves, aqueous PEI salt solutions and brominated poly(2,6-dimethylphenylene oxide) form stable emulsions from which it is possible to cast membranes in which submicrometer capsules of the salt solution ate embedded (455). The rate of release of the salt solution can be altered by surface—active substances. In membranes, PEI can act as a proton source in the generation of a photocurrent (456). The formation of a PEI coating on ion-exchange membranes modifies the transport properties and results in permanent selectivity of the membrane (457). The electrochemical testing of salts (458) is another possible appHcation of PEI. 

Waste Treatment. Environmental concerns have increased the need to treat Hquid discharges from all types of industrial processes, as well as mnoffs where toxic substances appear as a result of leaks or following solubilization (see Wastes, industrial). One method of treatment consists of an ion-exchange system to remove the objectionable components only. Another involves complete or partial elimination of Hquid discharges by recycling streams within the plant. This method is unacceptable unless a cycHc increase in the impurities is eliminated by removing all constituents prior to recycling. 

The potentiometry sensor (ion-selective electrode) controls application for determination of polymeric surface-active substances now gets the increasing value. Potentiometry sensor controls are actively used due to simple instmment registration, a wide range of determined concentrations, and opportunity of continuous substances contents definition. That less, the ionometry application for the cation polymeric SAS analysis in a solution is limited by complexity of polycation charge determination and ion-exchanger synthesis. 

Ion Exchange. Certain solid substances have the property of exchanging one ion for another if placed in a solution containing the ions. Typical substances with this property are the zeolites and certain synthetic resins. 

The extent to which one ion is absorbed in preference to another is of fundamental importance it will determine the readiness with which two or more substances, which form ions of like charge, can be separated by ion exchange and also the ease with which the ions can subsequently be removed from the resin. The factors determining the distribution of inorganic ions between an ion exchange resin and a solution include ... 

Many organic compounds are only slightly soluble in water so that non-aqueous ion exchange has an important role in operations with organic substances.21... 

With flame emission spectroscopy, there is greater likelihood of spectral interferences when the line emission of the element to be determined and those due to interfering substances are of similar wavelength, than with atomic absorption spectroscopy. Obviously some of such interferences may be eliminated by improved resolution of the instrument, e.g. by use of a prism rather than a filter, but in certain cases it may be necessary to select other, non-interfering, lines for the determination. In some cases it may even be necessary to separate the element to be determined from interfering elements by a separation process such as ion exchange or solvent extraction (see Chapters 6, 7). 

Separation techniques may have to be applied if the given sample contains substances which act as interferences (Section 21.10), or, as explained above, if the concentration of the element to be determined in the test solution is too low to give satisfactory absorbance readings. As already indicated (Section 21.10), the separation methods most commonly used in conjunction with flame spectrophotometric methods are solvent extraction (see Chapter 6) and ion exchange (Chapter 7). When a solvent extraction method is used, it may happen that the element to be determined is extracted into an organic solvent, and as discussed above it may be possible to use this solution directly for the flame photometric measurement. 

Samsonov GV, Trostianskaya EB, Elkin GE (1969) Ion Exchange. Sorption of Organic Substances. (In Russian) Nauka... 

The neutral surfactant is measured after fixing of the ionic substances on a combined anionic/cationic ion exchange column. Volatile substances in the eluate are determined by gas chromatography and nonvolatile substances are measured gravimetrically. In the bulk of the neutral compounds phosphoric acid triesters may be present. This part is additionally determined by atom emission spectroscopy. 

As the solvent mixture also contained 225 mg of tetramethyl ammonium hydroxide pentahydrate per liter at a high water content (75%), the surface of the reverse phase would have been largely covered with the tetramethyl ammonium hydroxide pentahydrate. This would have acted as an adsorbed ion exchange stationary phase. It is clear that the free acids, salicylic acid, acetylsalicylic acid (aspirin) and benzoic acid were retained largely by ionic interactions with adsorbed basic ion exchanger and partly by dispersive interactions with the exposed reversed phase. The acetaminophen and the caffeine, on the other hand, being unionized substances, were retained only by dispersive interactions with the exposed reversed phase. 

Complete resolution was not achieved due to the carryover of interfering substances which frequently occurs when separating the components of biological samples. The column carried a reverse phase, but as the mobile phase contained low concentrations of lauryl sulfate, some would have adsorbed on the surface of the stationary phase and significantly modified its interacting properties. The retention mechanism is likely to have involved both ionic interactions with the adsorbed ion exchanger together with dispersive interactions with any exposed areas of the reverse phase. 

---