0000000000459795
AUTHOR
M. Moya-moreno
showing 4 related works from this author
Voltammetric Identification of Lead(II) and (IV) in Mediaeval Glazes in Abrasion-Modified Carbon Paste and Polymer Film Electrodes. Application to th…
2000
Direct identification of lead(II) and (IV) in glazed ceramics by cyclic voltammetry and differential pulse voltammetry is described. Characteristic cathodic and anodic profiles are obtained for microsample coatings in Paraloid B72-film electrodes immersed in NaCl and HAc/NaAc media. The electrochemical response of PbO, PbO2 and Pb3O4, and a series of test specimens of glaze is compared with that of microsamples extracted from the glaze of blue and white decorated ceramic produced in Manises (Spain) in the 15th century which have been buried in a damp place. Under abrasive conditions, striping peaks at –0.12 and –0.25 V (vs. SCE) appear for Pb(IV) centers and, at –0.55 and –0.75 V, for Pb(II…
Identification of inorganic pigments from paintings and polychromed sculptures immobilized into polymer film electrodes by stripping differential pul…
2000
Abstract Inorganic pigments in paintings and polychromed sculptures are studied by cyclic voltammetry and differential pulse stripping voltammetry using micro-sample coatings in Paraloid B72-film modified electrodes. Characteristic cathodic and anodic differential pulse profiles were obtained in the +0.4 to −1.0 V vs. SCE potential range for different cadmium, copper, lead, mercury and zinc pigments used in traditional colour palettes. Under optimized conditions, excellent reproducibility was obtained. Microsamples extracted from polychromed sculptures, wall paintings, canvas paintings, panel paintings and altarpieces from Spain, Ethiopia and Italy from the 12th to the 20th centuries have b…
Determination of the Boron/Lead Ratio in Ceramic Materials Based on Electrochemical Quartz Crystal Microbalance
2004
A method for quantitatively determining the relationship boron/lead in ceramic materials is presented. It is based on the attachment of microsamples of ceramic frits to an electrochemical quartz crystal microbalance (EQCM). After a reductive deposition step in the � 0.25 to � 0.85 V (vs. AgCl/Ag) potential range, well-defined stripping peaks are recorded in 0.10 M NaCl plus 0.10 M mannitol. The deposition of boron and lead from suspensions of solid materials, and its subsequent oxidative dissolution can be monitorized at the EQCM. The quotient between the maximum mass gain and the corresponding charge passed enables for a direct quantitation of the boron/lead molar ratio in ceramic material…
Electrochemical determination of boron in minerals and ceramic materials
2004
Abstract A method for quantitatively determining boron in minerals and ceramic materials is described. It is based on the abrasive attachment of mixtures of ZnO plus sample to PIGEs. After a reductive deposition step, square wave voltammograms recorded for those modified electrodes immersed into 0.10 M NaCl+0.25 M mannitol provide well-defined stripping peaks at −0.85 and −0.15 V vs. AgCl/Ag for the oxidation of Zn and B, respectively. The quotients between the peak areas and the peak currents for the stripping oxidation of B and Zn vary linearly with the molar ratio of B and Zn in the mixture, thus providing an electrochemical method for determining the boron content in solid samples. Resu…