G
Guido Viscardi
Researcher at University of Turin
Publications - 183
Citations - 4375
Guido Viscardi is an academic researcher from University of Turin. The author has contributed to research in topics: Dyeing & Aqueous solution. The author has an hindex of 35, co-authored 176 publications receiving 3832 citations. Previous affiliations of Guido Viscardi include Wroclaw University of Environmental and Life Sciences.
Papers
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Journal ArticleDOI
Photoanode/Electrolyte Interface Stability in Aqueous Dye‐Sensitized Solar Cells
Simone Galliano,Federico Bella,Claudio Gerbaldi,M. Falco,M. Falco,Guido Viscardi,Michael Grätzel,Claudia Barolo +7 more
TL;DR: In this paper, nine different sensitizers, selected based on their different properties in terms of light absorption, chemical structure, and hydrophobic/hydrophilic nature, are systematically investigated to identify some useful guidelines to choose and design suitable dyes of different colors for truly aqueous DSSCs.
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Properties of novel azodyes containing powerful acceptor groups and thiophene moiety
Isabelle Ledoux,J. Zyss,Ermanno Barni,Claudia Barolo,N. Diulgheroff,Pierluigi Quagliotto,Guido Viscardi +6 more
TL;DR: In this paper, an approach to design improved nonlinear optical chromophores is based on the employment of both strong acceptor group and thiophene ring instead of benzene in a mixed azobenzene-stilbene like chromogen.
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Determination of banned Sudan dyes in food samples by molecularly imprinted solid phase extraction-high performance liquid chromatography
Claudio Baggiani,Laura Anfossi,Patrizia Domenica Baravalle,Cristina Giovannoli,Gianfranco Giraudi,Claudia Barolo,Guido Viscardi +6 more
TL;DR: The optimized extraction protocol resulted in a reliable molecularly imprinted SPE (MISPE) method suitable for HPLC analysis, and was selective for the main analyte, Sudan I, and the related azo-dyes Sudan II, III, IV, Sudan Red B, and Sudan Red 7B, while the permitted azo -dyes Allura Red AC, Neococcin, and Sunset Yellow FCF were not extracted.
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Photophysical properties and computational investigations of tricarbonylrhenium(I)[2-(4-methylpyridin-2-yl)benzo[d]-X-azole]L and tricarbonylrhenium(I)[2-(benzo[d]-X-azol-2-yl)-4-methylquinoline]L derivatives (X = N–CH3, O, or S; L = Cl−, pyridine)
Andrea Albertino,Claudio Garino,Simona Ghiani,Roberto Gobetto,Carlo Nervi,Luca Salassa,Edward Rosenberg,Ayesha Sharmin,Guido Viscardi,Roberto Buscaino,Gianluca Croce,Marco Milanesio +11 more
TL;DR: In this paper, a combined experimental and computational study of new rhenium tricarbonyl complexes based on the bidentate heterocyclic N-N ligands 2-(4-methylpyridin-2-yl)benzo[ d ]-X-azole (X = N-CH 3, O, or S) and 2-(benzo-d ]-x-azol-2 -yl)-4 -methylquinoline (X= N−CH 3, O or S).
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Oxidative degradation of Remazol Turquoise Blue G 133 by soybean peroxidase.
Tatiana Marchis,Paola Avetta,Alessandra Bianco-Prevot,Debora Fabbri,Guido Viscardi,Enzo Laurenti +5 more
TL;DR: This analysis showed that the enzyme catalyses the breaking of the phthalocyanine ring producing sulfophthalimide as the main degradation product, and the release of stoichiometric amount of ammonium and Cu(II) ions.