The influence of the nature of the di- and trivalent metals and of the interlayer anion of different hydrotalcite-like (HT) clays on the anion-exchange ability is investigated. In view of the application of similar clays as electrode coatings in electroanalysis and electrocatalysis, the responses of electrodes modified with the different HT to electroactive species in solution constitute the primary source of information. However, XRD measurements have proved to be invaluable tools when coupled with the electrochemical data. Two organic and one inorganic anion with reversible redox behaviour, i.e. anthraquinone mono-and disulphonates and hexacyanoferrate(II), have been chosen as electroactive species. (C) 1998 Elsevier Science S.A. All rights reserved.

Electrodes coated by hydrotalcite-like clays. Effect of the metals and the intercalated anions on ion accumulation and retention capability

Gazzano M;
1998

Abstract

The influence of the nature of the di- and trivalent metals and of the interlayer anion of different hydrotalcite-like (HT) clays on the anion-exchange ability is investigated. In view of the application of similar clays as electrode coatings in electroanalysis and electrocatalysis, the responses of electrodes modified with the different HT to electroactive species in solution constitute the primary source of information. However, XRD measurements have proved to be invaluable tools when coupled with the electrochemical data. Two organic and one inorganic anion with reversible redox behaviour, i.e. anthraquinone mono-and disulphonates and hexacyanoferrate(II), have been chosen as electroactive species. (C) 1998 Elsevier Science S.A. All rights reserved.
1998
chemically modified electrodes
anionic clays
hydrotalcites
LAYERED DOUBLE HYDROXIDES
CHEMICALLY MODIFIED ELECTRODES
ORGANIC-ANIONS
PRECURSORS
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/212010
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 54
social impact