“…9) that remain in the second or more scans, and which disappear only after a long time in solution. In agreement with the literature [23][24][25][26][27] it is concluded that the hydrazo compound generated in alkaline medium is stable enough to be detected by cyclic voltammetry. A similar behavior is observed in neutral conditions but not in acidic medium.…”
“…After extraction of the completely reduced (electrolysis at pH 10) dye solution with chloroform the UV-vis spectra were compared with the literature [21,27]. A small quantity of phenylenediamine intermediate was detected in the chloroform phase in aliquots preelectrolyzed in neutral and alkaline solution using its typical UV spectrum with an adsorption maxima at l ¼ 270 nm [24] as identification. On the other hand, sulfanilic acid was identified in the aqueous phase in all electrolyzed solutions in acidic, neutral or alkaline solution by a high absorption peak verified in the spectrum at 238 nm [21,27].…”
“…9) that remain in the second or more scans, and which disappear only after a long time in solution. In agreement with the literature [23][24][25][26][27] it is concluded that the hydrazo compound generated in alkaline medium is stable enough to be detected by cyclic voltammetry. A similar behavior is observed in neutral conditions but not in acidic medium.…”
“…After extraction of the completely reduced (electrolysis at pH 10) dye solution with chloroform the UV-vis spectra were compared with the literature [21,27]. A small quantity of phenylenediamine intermediate was detected in the chloroform phase in aliquots preelectrolyzed in neutral and alkaline solution using its typical UV spectrum with an adsorption maxima at l ¼ 270 nm [24] as identification. On the other hand, sulfanilic acid was identified in the aqueous phase in all electrolyzed solutions in acidic, neutral or alkaline solution by a high absorption peak verified in the spectrum at 238 nm [21,27].…”
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