0000000000234248

AUTHOR

Claudio Baiocchi

0000-0002-8850-4654

showing 4 related works from this author

Azo-Dyes Photocatalytic Degradation in Aqueous Suspension of TiO2 Under Solar Irradiation

2002

Abstract The photodegradation of two common and very stable azo-dyes, i.e. methyl-orange (C14H14N3SO3Na) and orange II (C16H11N2SO4Na), is reported. The photocatalytic oxidation was carried out in aqueous suspensions of polycrystalline TiO2 irradiated by sunlight. Compound parabolic collectors, installed at the “Plataforma Solar de Almeria” (PSA, Spain) were used as the photoreactors and two identical reacting systems allowed to perform photoreactivity runs for the two dyes at the same time and under the same irradiation conditions. The disappearance of colour and substrates together with the abatement of total organic carbon content was monitored. The main sulfonate-containing intermediate…

Environmental EngineeringPhotochemistryHealth Toxicology and MutagenesisPhotochemistryHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundMethyl orangeEnvironmental ChemistryIrradiationColoring AgentsPhotodegradationTitaniumAqueous solutionBenzenesulfonatesPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollutionchemistryTitanium dioxideSunlightPhotocatalysisIndicators and ReagentsAzo CompoundsOxidation-ReductionWater Pollutants Chemical
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Analytical control of photocatalytic treatments: degradation of a sulfonated azo dye

2003

The degradation of Methyl Orange (C(14)H(14)N(3)SO(3)Na), chosen as a model sulfonated azo dye, was investigated in aqueous solutions containing suspended polycrystalline TiO(2) particles under irradiation with simulated sunlight. The dye disappearance and the formation of the mineralization end products were monitored; the formation of the main transient intermediates was also examined in detail. Particular attention was devoted to the identification and to the evolution of fragments retaining the chromophoric group. The comparison of data coming from various analytical techniques led to a possible reaction mechanism for the degradation process, giving insight into an aspect of the treatme…

Reaction mechanismAqueous solutionMineralization (soil science)PhotochemistryBiochemistryAnalytical Chemistrychemistry.chemical_compoundchemistryPhotodegradationMethyl orangePhotocatalysisazo dyeDegradation (geology)Organic chemistryCrystalliteIrradiationPhotocatalysis
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Characterization of methyl orange and its photocatalytic degradation products by HPLC/UV–VIS diode array and atmospheric pressure ionization quadrupo…

2002

Abstract HPLC/UV–VIS diode array and HPLC/MS techniques were successfully applied to the analysis of sulfonated molecules present in samples coming from the photocatalytic degradation of the azo dye indicator, methyl orange. The substrate was chosen as a simple model for the study of reactions involving the more complex commercial products used for the dyeing of textile fibers. Unexpected MS fragmentation path was observed, due to the very stable methyl orange molecular structure. The chromatographic information were combined with the obtained MS, MS/MS data and the UV–VIS diode array spectra and allowed to rationalize the molecular structures attributable to the various degradation product…

Atmospheric pressureChemistryAnalytical chemistrySubstrate (chemistry)Condensed Matter PhysicsMass spectrometryHigh-performance liquid chromatographychemistry.chemical_compoundIonizationMethyl orangePhysical and Theoretical ChemistryQuadrupole ion trapDyeingInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Photocatalytic degradation of acid blue 80 in aqueous solutions containing TiO2 suspensions.

2001

The photocatalytic degradation of the anthraquinonic dye Acid Blue 80 in aqueous solutions containing TiO2 dispersions has been investigated. The process has been monitored by following either the disappearance of the dye (via HPLC) and the formation of its end-products (via IC, GC, and TOC analysis). Although a relatively fast decolorization of the solutions has been observed, the mineralization is slower, and the presence of residual organic compounds was evidenced even after long term irradiation, confirming the relevant stability of anthraquinone derivatives. The identification of various unstable intermedi ates formed after low irradiation times was performed by HPLC-MS, allowing us to…

TitaniumReaction mechanismAqueous solutionPhotolysisSubstrate (chemistry)AnthraquinonesGeneral ChemistryMineralization (soil science)PhotochemistryHeterogeneous catalysisHydroxylationCatalysisHydroxylationchemistry.chemical_compoundchemistryPhotocatalysisEnvironmental ChemistryOrganic chemistryColoring AgentsWater Pollutants ChemicalEnvironmental sciencetechnology
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