Search results for "Roche"

showing 10 items of 2666 documents

Multiple-scan voltammetry and OCP: Archaeometric tools for dating archaeological bronzes

2021

[EN] The application of a multiple-scan strategy to nanosamples taken from 18 cross-sections of Bronze Age arms and armour, as well as two Roman coins using two solid-state electrochemical techniques, the voltammetry of immobilized microparticles (VIMP) and open circuit potential measurements (OCP) is described. The voltammetric responses in contact with aqueous acetate buffer can be attributed to the reduction of cuprite with variable degree of compaction and crystallinity revealing significant differences in the gradient of such properties with depth. Such differences are also revealed by "dry" OCP measurements connecting points in the cross section near and separated from the corrosion l…

Bronze AgeDating archaeological bronzesCupriteGeneral Chemical Engineeringchemistry.chemical_elementContext (language use)02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesAnalytical ChemistryCorrosionCrystallinityElectrochemistryBronzeCorrosion studiesVoltammetryDeposition (law)Voltammetry of immobilized particlesMetallurgy021001 nanoscience & nanotechnologyCopper0104 chemical scienceschemistryPINTURAvisual_artOCPvisual_art.visual_art_mediumengineering0210 nano-technologyJournal of Electroanalytical Chemistry
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A Solar Photothermocatalytic approach for the CO2 conversion: Investigation of different synergisms on CoO-CuO/Brookite TiO2-CeO2 catalysts

2022

Abstract The photoactive features of the least common polymorph of TiO2, i.e. brookite, were combined with the thermocatalytic redox ones of cerium oxide, focusing on the effects of the addition of small amounts of Co-Cu oxides for the solar CO2 conversion. By considering the characterization data, a surface segregation of the hosted metal oxides on the TiO2-CeO2 composite was evidenced, and their presence increased the amount of oxygen vacancies and improved the charge carriers separation. The bimetallic oxides-based sample was the most performing one in the photocatalytic carbon dioxide reduction at room temperature. The formation of carbon monoxide and methane was 5 and 0.5 μmol g−1h−1, …

Brookite TiO2Cerium oxideMaterials scienceBrookiteGeneral Chemical EngineeringBimetallic oxidesGeneral ChemistryIndustrial and Manufacturing EngineeringMethaneCatalysisPhotothermo-catalysischemistry.chemical_compoundchemistryChemical engineeringvisual_artPhotocatalysisvisual_art.visual_art_mediumEnvironmental ChemistryCO2valorizationBimetallic stripCarbon monoxideElectrochemical reduction of carbon dioxideCeO2
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Bulk deposition at the industrial area of Gela (southern Sicily, Italy): preliminary results

2009

Bulk depositionTrace elementsPetrochemical plantGela
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Standard additions-dilution method for absolute quantification in voltammetry of microparticles. Application for determining psychoactive 1,4-benzodi…

2013

A standard additions-dilution solid-state electrochemical method for the determination of psychoactive 1,4-benzodiazepine and antidepressants drugs used as adulterants in commercial slimming herbal formulations is described and compared with conventional standard addition method. The proposed method, based on the voltammetry of microparticles approach, permits quantify, via standard additions methodology, 1,4-benzodiazepine and antidepressants drugs in phytotherapeutic formulations with no need of sample dissolution using dilution with a reference electroactive compound. The method was used to measure 1,4-benzobenzodiazepines (clonazepam, flurazepam, alprazolam, midazolam, bromazepam, chlor…

BupropionBromazepamBenzodiazepineFlurazepamChemistrymedicine.drug_classClinical BiochemistryPharmaceutical ScienceLorazepamElectrochemical TechniquesPharmacologyAntidepressive AgentsClonazepamAnalytical ChemistryBenzodiazepinesAlprazolamStandard additionDrug DiscoverymedicinePlant PreparationsDrug ContaminationBrazilSpectroscopymedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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Cationic and Zwitterionic Polymerizable Surfactants:  Quaternary Ammonium Dialkyl Maleates. 1. Synthesis and Characterization

1999

Cationic and zwitterionic reactive dialkyl maleates with different hydrophobic chain lengths (R = C10H21, C12H25, C16H33, and C18H37), and some similar surfactants without double bonds were synthesized with an aim to use them as stabilizers in the batch and seeded emulsion copolymerization of styrene and butyl acrylate (part 2 of this series). Surfactants are obtained in a three-step synthesis, starting from ring opening of maleic anhydride, followed by O alkylation with an aminoalkyl compound, and finishing with quaternization of the amino group in the hydrophilic part of the molecule. The chemical structure of surfactants was confirmed by 1H NMR. Melting points and critical micelle concen…

Butyl acrylateCationic polymerizationMaleic anhydrideSurfaces and InterfacesCondensed Matter PhysicsMicelleStyrenechemistry.chemical_compoundPulmonary surfactantchemistryElectrochemistryCopolymerOrganic chemistryGeneral Materials SciencePolystyreneSpectroscopyLangmuir
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Electrochemical Synthesis of 2-Hydroxy-para-terphenyls by Dehydrogenative Anodic C–C Cross-Coupling Reaction

2019

The anodic C–C cross-coupling reaction provides fast access to a wide range of bi- and terarylic scaffolds by electrochemically mediated arylation reactions. Herein, a metal- and reagent-free electrosynthetic protocol for the synthesis of nonsymmetrical 2-hydroxy-para-teraryl derivatives is presented for the first time. It is scalable, easy to conduct, and allows the use of a broad variety of different functional groups.

C c coupling010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCoupling reaction0104 chemical sciencesAnodeSynlett
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Chemical Identification at the Solid–Liquid Interface

2017

Solid-liquid interfaces are decisive for a wide range of natural and technological processes, including fields as diverse as geochemistry and environmental science as well as catalysis and corrosion protection. Dynamic atomic force microscopy nowadays provides unparalleled structural insights into solid-liquid interfaces, including the solvation structure above the surface. In contrast, chemical identification of individual interfacial atoms still remains a considerable challenge. So far, an identification of chemically alike atoms in a surface alloy has only been demonstrated under well-controlled ultrahigh vacuum conditions. In liquids, the recent advent of three-dimensional force mapping…

CALCIUM-CARBONATEMOLECULAR-DYNAMICS SIMULATIONSSURFACEInterface (Java)AlloyNanotechnology02 engineering and technologyengineering.material010402 general chemistry53001 natural sciencesAQUEOUS-SOLUTIONCorrosionElectrochemistryWATERGeneral Materials ScienceFIELDSpectroscopySpectroscopySolid liquidATOMIC-FORCE MICROSCOPYta114ChemistryAtomic force microscopyHYDRATIONSolvationSurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesRESOLUTIONengineeringIdentification (biology)0210 nano-technologyLangmuir
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Effect of temperature on the passive state of Alloy 31 in a LiBr solution: Passivation and Mott-Schottky analysis

2015

The passive behaviour of Alloy 31, a highly-alloyed austenitic stainless steel (UNS N08031), has been investigated in a LiBr heavy brine (700 g/l) at different temperatures using potentiostatic polarisation and Mott-Schottky analysis. Cation vacancies have been found to be the dominant defect in the passive films formed on Alloy 31. An increase in temperature enhanced the generation of cation vacancies at the film/solution interface and raised the steady-state passive current density. The density of defects within the passive film also increased significantly with temperature, making the film more conductive and less protective against localised attacks.

CARBON-STEELAUSTENITIC STAINLESS-STEELBORATE BUFFER SOLUTIONOXIDE-FILMSINGENIERIA QUIMICAElectroquímicaPOINT-DEFECT MODELELECTRONIC-STRUCTUREREPASSIVATION KINETICSELECTROCHEMICAL-IMPEDANCE SPECTROSCOPYPOTENTIAL DISTRIBUTIONACTIVITY-COEFFICIENTSAcer Corrosió
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How far are we from the valorization of waste-CO2 to formic acid via electrochemical routes for the applicative scale?

To date, the decarbonization of the world economy and storage and production of energy from alternative C-based sources is considered a relevant topic. The electrochemical conversion of CO2 has been widely investigated since the 1870s as a promising strategy to convert waste-CO2 into value-added chemicals [1,2]. Recently, it was highlighted that, among the several emerging technologies for CO2 conversion to value-added products on an applicative scale, electrochemical technologies are the closest to commercialization due to the numerous start-ups and established companies being invested in this area (e.g., Opus-12, Dioxide Material, and Carbon Recycling International) [3]. These technologie…

CO2 conversion electrochemistry Formic acid pressure GDESettore ING-IND/27 - Chimica Industriale E Tecnologica
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Cathodic reduction of CO2 to formic acid: Effect of the nature of the cathode for pressurized systems

2023

Electrochemical conversion of CO2 into formic acid (FA) in an aqueous electrolyte is considered a promising strategy to valorise waste-CO2. Some studies, mainly performed using Sn cathodes, have shown that the performance of the process can be strongly improved using pressurized systems. On the other hand, other studies, usually carried out in non-pressurized systems, have indicated that the nature of the cathode can strongly affect the process. Hence, in this work, we have investigated the coupled effect of nature of the cathode and CO2 pressure (PCO2 ) on the electrochemical conversion of CO2 to FA. Four electrodes (Sn, Sn/C-NP, Bi, Bi/C-NP) have been used as model cathodes. The results o…

CO2 reductionFormic acidPressureTinBismuthElectrochemistryCO2 reductionTinProcess Chemistry and TechnologyPressureElectrochemistryChemical Engineering (miscellaneous)Formic acidSettore ING-IND/27 - Chimica Industriale E TecnologicaBismuthPollutionWaste Management and DisposalJournal of Environmental Chemical Engineering
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