Extraction cation-exchanging

Before polyacrylamides are sold, the amount of residual acrylamide is determined. In one method, the monomer is extracted from the polymer and the acrylamide content is determined by hplc (153). A second method is based on analysis by cationic exchange chromatography (154). For dry products the particle si2e distribution can be quickly determined by use of a shaker and a series of test sieves. Batches with small particles can present a dust ha2ard. The percentage of insoluble material is determined in both dry and emulsion products. 

A.cidic Extractants. Acidic extractants, HE, react with REE according to a cation-exchange reaction ... 

Recovery and Purification. The dalbaheptides are present in both the fermentation broth and the mycelial mass, from which they can be extracted with acetone or methanol, or by raising the pH of the harvested material, eg, to a pH of 10.5—11 for A47934 (16) (44) and A41030 (41) and actaplanin (Table 2) (28). A detailed review on the isolation of dalbaheptides has been written (14). Recovery from aqueous solution is made by ion pair (avoparcin) or butanol (teicoplanin) extraction. The described isolation schemes use ion-exchange matrices such as Dowex and Amberlite IR, acidic alumina, cross-linked polymeric adsorbents such as Diaion HP and Amberlite XAD, cation-exchange dextran gel (Sephadex), and polyamides in various sequences. Reverse-phase hplc, ion-exchange, or affinity resins may be used for further purification (14,89). 

Solvent Recovery. A mixture of methanol and methyl acetate is obtained after saponification. The methyl acetate can be sold as a solvent or converted back into acetic acid and methanol using a cationic-exchange resin such as a cross-linked styrene—sulfonic acid gel (273—276). The methyl acetate and methanol mixture is separated by extractive distillation using water or ethylene glycol (277—281). Water is preferred if the methyl acetate is to be hydroly2ed to acetic acid. The resulting acetic acid solution is concentrated by extraction or a2eotropic distillation. 

SG sols were synthesized by hydrolysis of tetraethyloxysilane in the presence of polyelectrolyte and surfactant. Poly (vinylsulfonic acid) (PVSA) or poly (styrenesulfonic acid) (PSSA) were used as cation exchangers, Tween-20 or Triton X-100 were used as non- ionic surfactants. Obtained sol was dropped onto the surface of glass slide and dried over night. Template extraction from the composite film was performed in water- ethanol medium. The ion-exchange properties of the films were studied spectrophotometrically using adsorption of cationic dye Rhodamine 6G or Fe(Phen) and potentiometrically by sorption of protons. 

Theory. Conventional anion and cation exchange resins appear to be of limited use for concentrating trace metals from saline solutions such as sea water. The introduction of chelating resins, particularly those based on iminodiacetic acid, makes it possible to concentrate trace metals from brine solutions and separate them from the major components of the solution. Thus the elements cadmium, copper, cobalt, nickel and zinc are selectively retained by the resin Chelex-100 and can be recovered subsequently for determination by atomic absorption spectrophotometry.45 To enhance the sensitivity of the AAS procedure the eluate is evaporated to dryness and the residue dissolved in 90 per cent aqueous acetone. The use of the chelating resin offers the advantage over concentration by solvent extraction that, in principle, there is no limit to the volume of sample which can be used. 

In an attempt to verify (or refute) this assumption, we have determined the thermodynamic parameters (AH, AS) for the complexes formed between Pu(III), Pu(IV), and HSOi in 1 M acid media utilizing cation-exchange and solvent extraction procedures. 

Stability constants of the complexes formed between Pu(III), Pu(IV), and HSOi, were determined in 1 M acid media by measuring the decrease in extraction (either into TTA-toluene or ion-exchange resin) with increasing concentration of HSO4 in the aqueous solution. Because of very different degrees of extraction for Pu(III) and Pu(IV) and the imposed requirement of 1 M acidity, Pu(IV)-HSOit complexation was studied by TTA extraction, while the Pu(III)-HSOit system was studied by cation exchange. 

Extraction of Aesculus hippocastanum L. (horse-chestnut) and purification on cation-exchanger (H -form), resp. precipitation with cholesterol. 

For an individual pesticide (e.g., carbendazim) or a limited class of pesticides (e.g., carbamates, benzoylphenylureas, pyrethroids ), it may be possible to optimize the SPE conditions so that the pesticide(s) are selectively retained on the cartridge. A wash step can be introduced to elute the matrix selectively, thus producing an extremely clean extract. For example, when cleaning up sample extracts for carbendazim analysis, a cation-exchange (SCX) cartridge may be used and the pH carefully controlled to retain the carbendazim firmly, whilst the co-extractives are washed to waste. The carbendazim residues can then be eluted from the column by adjusting the pH. 

Another material based on the crown ether extractant 4,4 (5 )-bis(t-butyl-cyclohexano)-18 crown-6, marketed under the name Sr-Spec, is useful for separations involving divalent cations including Pb, Ba, and Ra (Horwitz et al. 1991). For Ra analysis by TIMS, Ra-Ba separations are required because the presence of Ba drastically decreases the ionization efficiency of fg Ra samples from 10% to <1%. This material has been widely used for separations of Ra from Ba (e.g., Chabaux et al. 1994 Lundstrom et al. 1998 Rihs et al. 2000 Joannon and Pin 2001 Pietruszka et al. 2002) and is a complement or alternative to cation exchange separations for EDTA complexes of these elements (Volpe et al. 1991 Cohen and O Nions 1991). Sr-Spec material would also be useful for °Pb analysis, since Pb has a greater distribution coefficient than Sr with this extractant. 

Strong cationic-exchange extraction and reversed-phase extraction (eliminates ion pairing when used in place of octadecyl silica. 

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