Extraction with mixed functionalities

Extraction by CMPO Calixarenes with Mixed Functionalities.279... 

An analytical solution for molecules with alkaline functionality is acid/base titration. In this technique, the polymer is dissolved, but not precipitated prior to analysis. In this way, the additive, even if polymer-bound, is still in solution and titratable. This principle has also been applied for the determination of 0.01 % stearic acid and sodium stearate in SBR solutions. The polymer was diluted with toluene/absolute ethanol mixed solvent and stearic acid was determined by titration with 0.1 M ethanolic NaOH solution to the m-cresol purple endpoint similarly, sodium stearate was titrated with 0.05 M ethanolic HC1 solution [83]. Also long-chain acid lubricants (e.g. stearic acid) in acrylic polyesters were quantitatively determined by titration of the extract. 

To improve chromatographic separation, another analytical column could be used in addition to the monolith (Xu et al. 2006). The monolith column served as an extraction column only. Hsieh et al. (2000, 2002) utilized a polymer-coated mixed function (PCMF) Capcell C8 column (4.6 x 50 mm, Phenomenex) to provide dual functions—online plasma extraction and analyte separation. The silica was coated with a polymer containing both hydrophilic polyoxythylene and hydrophobic groups. The diluted plasma samples (1 1 to 1 3) were injected directly. No column deterioration was observed after 200 injections. 

Saponification (see Section 7.4) is carried out to extract more recalcitrant lipids, and the yields are higher than for conventional solvent extraction (Stern et al. 2000). 3 ml of 0.5 M methanolic NaOH is added to 0.1 g of the shard powder and heated at 70°C for 3 hours in a sealed glass vial. After cooling, the supernatant is acidified with HC1 and extracted with three aliquots of 3 ml //-hexane. The hexane will not mix with the methanolic solution (unlike the DCM MeOH used above), but will absorb the lipids and can be transferred into a new clean vial. The removal of excess hexane is carried out as above. Saponification will hydrolyze and methylate any ester functionalities, which removes the requirement to derivatize the samples (Section 7.4) unless other molecules are suspected of being present. However, any wax esters or triacylglycerols will also be hydrolyzed to their fatty acid methyl esters and alcohols therefore, if information on their composition is required, then conventional solvent extraction is recommended as a first step. For subsequent characterization of the lipid extract, see Chapter 7. 

Chakraborty et al. [76] also found that degree of chromiuin(VI) extraction is a function of time in acidic pH with the extractants Aliquat 336, tri- -octyl amine and their mixtures (see Fig. 4.9). Furthermore, a slight synergistic effect was observed when the two extractants were mixed. Valenzuela et al. [77] studied that the initial copper extraction rate was proportional to the concentration of oximic carrier in the organic phase and to the metal content in the acid mine drainage. 

Imprinted polymer membranes are prepared using atrazine as the template, methacrylic acid as a functional monomer, and tri(ethylene glycol) dimethacrylate (TEDMA) as a cross-linker. The molar ratio of the functional monomer to the template is 5 1. This ratio has to be optimized for each template. In order to obtain thin, flexible and mechanically stable membranes, oligourethane acrylate (molecular mass 2600) is added to the monomer mixture. Preparation of the molecularly imprinted polymer membrane is done as follows. Atrazine (20 mg) is mixed with methacrylic acid (40 mg), TEDMA (289 mg), oligourethane acrylate (51 mg), AIBN (2 mg) and 30% v/v of chloroform. Then a 60-120 pm gap between two quartz slides is filled with the monomer mixture. To initiate polymerization, the slides with the mixture are exposed to UV radiation (365 nm, intensity 20 W m ) for 30 min. After polymerization, atrazine is extracted with ethanol in a Soxhlet apparatus for 2h. This should not cause any visible changes in the MIP membrane. A membrane for control experiments can be prepared similarly except that no atrazine is added to the monomer mixture. 

Appreciable quantities of alkanes are ingested by animals as constituents of plant material and also by man as artificial additives (e.g. mineral oils) of foodstuffs or as components of natural or artificially produced oils and fats. Very little is known about the details of the metabolic turnover of such compounds. As in micro-organisms, it is likely that alkanes are detoxified in animals and plants by a mixed-function oxidase which forms the alcohols that may be further metabolized or excreted in the urine as conjugates, such as glucoronides or sulphates. Most of the compounds reported were characterized (GC-MS) after extraction from urine fractions that had been incubated with the appropriate enzyme to cleave the conjugate. Some biotransformations of alkanes by animal systems (mainly in vivo) are summarized in Figure 7. 

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