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Frans_M_Everaerts_Isotachophoresis_378342.pdf

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AMINO ACIDS<br />

Fig.13.3. Schematic diagram illustrating that mixed zones are found in isotachophoretic analyses if<br />

the differences in effective mobilities are too small. A black square indicates that a mixed zone is<br />

obtained between that pair of amino acids if they are present in one sample. The experiments were<br />

carried out in the operational system listed in Table 13.3.<br />

are too small. If so, a method may be found for determining complexation constants in<br />

isotachophoretic analyses by varying the field strength in various experiments.<br />

13.1.5. Separation in aqueous propanal solutions<br />

It is well known that amino acids easily form complexes (Schiff bases) with aldehydes.<br />

If amino acids are dissolved in a solution that contains an aldehyde, differences in<br />

mobility can be expected because the solvent property changes, the amino acid molecule<br />

is larger after complex formation and its pZ value changes because the complex is formed<br />

with the amino group(s). The first two effects result in a small difference and the last<br />

effect in a large difference in mobility. The last effect occurs at very low concentrations<br />

of the aldehyde, assuming that the aldehyde character is great enough.<br />

Experiments with sugars did not show substantial differences in the effective mobilities<br />

of the various amino acids, especially if they were added in relatively low concentrations.<br />

Formaldehyde, which has a strong aldehyde character, and acetaldehyde were found<br />

to be very unstable. Even during analysis, formic acid and acetic acid, respectively, are<br />

formed. Research is continuing to find a suitable combination of a non-ionic stabilizer(s)<br />

in order to work reproducibly with formaldehyde and acetaldehyde.<br />

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