http://www.cnr.it/ontology/cnr/individuo/prodotto/ID71984
Carbon paste electrode bulk modified with a conducting polymer poly(1,8-diaminonaphthalene): application to lead determination (Articolo in rivista)
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- Carbon paste electrode bulk modified with a conducting polymer poly(1,8-diaminonaphthalene): application to lead determination (Articolo in rivista) (literal)
- Anno
- 2003-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1007/s00604-003-0058-5 (literal)
- Alternative label
SanaĆ¢. Majid , Mamia El Rhazi , Aziz. Amine , Antonella Curulli , Giuseppe Palleschi (2003)
Carbon paste electrode bulk modified with a conducting polymer poly(1,8-diaminonaphthalene): application to lead determination
in Mikrochimica acta (1966, Print); Springer, New York (Stati Uniti d'America)
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- SanaĆ¢. Majid , Mamia El Rhazi , Aziz. Amine , Antonella Curulli , Giuseppe Palleschi (literal)
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- Univ Hassan II, Fac Sci & Tech, Mohammadia, Morocco
Ist Studio Mat Nanostrutturati, Sez Roma 2, CNR ISMN, I-00161 Rome, Italy
Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy (literal)
- Titolo
- Carbon paste electrode bulk modified with a conducting polymer poly(1,8-diaminonaphthalene): application to lead determination (literal)
- Abstract
- Carbon paste electrodes modified with conducting polymers for sensitive and selective determination of lead are presented. A novel method for generating a reproducible polymer-coated electrode surface is developed. We prove that 1,8-diaminonaphthalene (1,8-DAN) mixed with a carbon paste electrode leads to a conducting polymer in acidic medium while, in the same medium, this polymer is known to be non-conducting on platinum electrode. The electrode behaviour of poly(1,8-DAN), electropolymerised into carbon paste, was investigated by cyclic voltammetry in the presence of the ferri-ferrocyanide couple.
A carbon paste electrode modified with poly(1,8-DAN) was used to determine Pb2+ in aqueous solutions. Pb2+ ions were firstly complexed and then electrochemically deposited by a potential step to -0.9 V. The accumulated lead after reduction was anodically stripped by differential pulse voltammetry. Different parameters, such as pH of the solution, preconcentration time, and electropolymerisation procedures were studied.
For a preconcentration time of ten minutes, the calibration graph was linear from 40 to 2070 ng mL(-1) with r(2)=0.998. The detection limit was found to be 30 ng mL(-1), and the relative standard deviation was 6%. (literal)
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