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   <subfield code="a">Electrochemical investigations on the analysis of reactive dyes with monoazo- and monoanthraquinone structures</subfield>
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   <subfield code="a">Summary: Qualitative voltammetric determination of reactive dyes is possible down to concentrations of about 10−5 mol/l using DC-polarography. Using rotating solid electrodes (glassy carbon) a detection limit of about 10−4 mol/l can be obtained. Reduction involves chiefly only the azo- and anthraquinoid groups, respectively, whereas the reactive functionality of these dyes shows electroactivity at much more negative potentials. Only the dichloro-quinoxaline group gives signals superimposed on the reduction of anthraquinoid groups. Discrimination between an original reactive dye and its hydrolysate (containing a hydrolytically destroyed reactive group) can be achieved, if the dye contains further cleavable groups such as benzamido substituents in conjugation to the chromophor as is seen with Azo-red I. Cleavage of such a group shifts the reduction potential for about 130 mV to more negative values.</subfield>
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