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   <subfield code="a">Electrochemical behaviour of persulphate on carbon paste electrodes modified with Prussian blue and analogous compounds</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[M. Weißenbacher, K. Kalcher, H. Greschonig, W. Ng, W. Chan, A. Voulgaropoulos]</subfield>
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   <subfield code="a">Summary: Peroxodisulphate (&quot;persulphate”) may be determined by direct current voltammetry (DCV) using carbon paste electrodes chemically modified with Prussian Blue, iron(III)-hexacyanoruthenate(II) or iron(III)-hexacyano-osmate(II). The determination is based on the exploitation of catalytic currents from the reduction of the modifiers. Best results are obtained for iron(III)-hexacyanoosmate(II) yielding a detection limit of 1 μg O 2 2− /ml (as persulphate) when using HCl (10−2 mol/l) as supporting electrolyte and measuring in the DCV-mode. Electrodes doubly-modified with the osmium compound and a liquid anion-exchanger (Amberlite LA2) allow determinations of persulphate after preconcentration under open circuit conditions, in the presence of hydrogen peroxide and perborate, with a detection limit of 20 ng O 2 2− /ml (as persulphate).</subfield>
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