Search results for "Oxidation."

showing 10 items of 1877 documents

A DFT investigation of CO oxidation over neutral and cationic gold clusters

2009

Abstract The interaction of CO and O 2 with neutral and positively charged Au 9 and Au 13 clusters was studied using Density Functional Theory. The aim was the understanding of the elementary steps of the low temperature activity of supported gold nanoparticles towards carbon monoxide combustion, that is, the oxidation of CO to CO 2 in presence of dioxygen molecules. The adsorption of a single CO molecule gives rise to a substantial electronic rearrangement on both neutral and cationic gold clusters. On the contrary, the adsorption of dioxygen produces an electron transfer from neutral gold clusters to the O 2 , while the interaction with cationic Au nanoparticles is simply electrostatic. C…

Gold clusterCationic polymerizationCondensed Matter PhysicsPhotochemistryBiochemistryChemical reactionCO oxidationDFTCatalysischemistry.chemical_compoundElectron transferAdsorptionchemistryMoleculePhysical and Theoretical ChemistryGold clusterCarbon monoxide
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Application of graphene quantum dots in heavy metals and pesticides detection

2020

Graphene Quantum Dots (GQDs) were produced using electrochemical oxidation of graphite rods. Obtained GQDs were gamma-irradiated in the presence of the N atoms source, ethylenediamine. Both structural and morphological changes were investigated using UV-Vis, X-ray photoelectron and photoluminescence (PL) spectroscopy as well as atomic force microscopy. The ability of both types of dots to change PL intensity in the presence of pesticides such as malathion and glyphosate, as well as copper (II) ions was detected. These preliminary results indicated a high potential of produced GQDs to be applied as non-enzymatic PL sensors for the detection of selected pesticides and metal ions. 26th Interna…

Graphene Quantum DotsX-ray photoelectron spectroscopymalathionatomic force microscopyphotoluminescence sensorsUV-Vis spectroscopycopper (II) ionglyphosatephotoluminescence spectroscopyGraphene Quantum Dotelectrochemical oxidationethylenediaminecopper (II) ionsgraphite rodgraphite rods
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Microbial impact on the isotope composition of methane in both thermal and hyperalkaline waters of central Greece

2019

Introduction The different origins of methane can be subdivided in biogenic (either directly produced by microbial activity or deriving by decay of organic matter at T > 150°C) and abiogenic (from pure inorganic reactions). Among the latter, one of the most debated origins comes from serpentinization processes of ultramafic rocks in ophiolitic sequences at low temperatures (T < 80 °C). Moreover, further secondary processes (diffusion, inorganic or microbial oxidation, etc.) may also contribute and thus mask the original chemical and/or isotope composition. Primary and secondary processes acting on CH4 can be recognised mainly through its isotope (d13C and d2H) composition and the rati…

Greece methane microbial oxidationSettore GEO/08 - Geochimica E Vulcanologia
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Developments in the dehydrogenative electrochemical synthesis of 3,3′,5,5′-tetramethyl-2,2′-biphenol

2021

Abstract The symmetric biphenol 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol is a well‐known ligand building block and is used in transition‐metal catalysis. In the literature, there are several synthetic routes for the preparation of this exceptional molecule. Herein, the focus is on the sustainable electrochemical synthesis of 3,3′,5,5′‐tetramethyl‐2,2′‐biphenol. A brief overview of the developmental history of this inconspicuous molecule, which is of great interest for technical applications, but has many challenges for its synthesis, is provided. The electro‐organic method is a powerful, sustainable, and efficient alternative to conventional synthesis to obtain this symmetric biphenol up to the …

Green chemistry540 Chemistry and allied sciencespolycycles010405 organic chemistryChemistryoxidationOrganic ChemistryC−C couplingMinireviewsGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesC c couplingelectrochemistry540 Chemiesustainable chemistryMinireviewC−C Coupling | Reviews Showcase
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Versatile Electrochemical C-H Amination via Zincke Intermediates.

2015

Simply by applying electricity, the amination reaction of a broad variety of arenes, heteroarenes, and benzylic substrates is achieved. Pyridine serves as the nitrogen source and the intermediate cationic species are well-protected from over-oxidation.

Green chemistryChemistryCationic polymerizationGeneral ChemistryElectrochemical TechniquesElectrochemistryCarbonCatalysischemistry.chemical_compoundPyridineOrganic chemistryOxidative coupling of methaneNitrogen sourceOxidation-ReductionAminationCopperAminationHydrogenAngewandte Chemie (International ed. in English)
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Waste-free electrochemical oxidation of alchools in water

2006

We describe a new sol-gel molecular electrode made of a thin layer of organosilica doped with the nitroxyl radical TEMPO (2,2,6,6-tetrame-thylpiperidine-1-oxyl) electrodeposited on the surface of an ITO-coated glass and its employment as a selective and versatile oxidation catalyst in the electrochemical conversion of different alcohols to carbonyl compounds. Environmentally friendly water or a water/acetonitrile mixture buffered with bicarbonate is used as solvent. The electrode is highly stable and it can be reused for a prolonged period of time allowing easy separation from the products.

Green chemistryChemistryalcoholgreen chemistryoxidationInorganic chemistryNitroxylGeneral ChemistryElectrochemistrycarbonyl compoundSolventchemistry.chemical_compoundCatalytic oxidationelectrochemistryAlcohol oxidationElectrodeAcetonitrileTEMPO
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Cluster Preface: Heterogeneous Catalysis

2016

International audience; Jean-Cyrille Hierso is full professor of Chemistry since 2009, heading the group of ‘Organometallic Chemistry and Catalysis’ at the Institute of Molecular Chemistry at the University of Bourgogne Franche-Comté (UBFC). He has interest in the fields of organometallic chemistry, ligand design, homo- and heterogeneous catalysis, chemical physics, and material sciences. In 2011 he was awarded the National Prize for Coordination Chemistry from the French Chemical Society (SCF), and at the end of 2012 he was elected a junior Member of the French Professors Academy ‘Institut Universitaire de France’ (IUF).Yasuhiro Uozumi is a full professor at the Institute for Molecular Sci…

Green chemistryMolecular chemistry010405 organic chemistryOrganic ChemistryLibrary scienceNanotechnology010402 general chemistryHeterogeneous catalysis01 natural sciencesMolecular science[ CHIM ] Chemical Sciences0104 chemical sciencesChemical societychemistry.chemical_compoundsustainable chemistry - nanocatalysts - organocatalysts - gold - palladium - nanoparticles - peptides - polymer supports - inorganic supports - nanotubes - epoxidation - esterification - cross-coupling - C–H functionalization - oxidation - (hetero)arenes - Kinetics - supramolecular assembly - recovery - recyclingchemistryTeam leader[CHIM]Chemical SciencesOrganometallic chemistry
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Photocatalytic Partial Oxidation of 5‐Hydroxymethylfurfural (HMF) to 2,5‐Diformylfuran (DFF) Over a Covalent Triazine Framework in Water

2020

Green chemistrychemistry.chemical_compoundChemistryCovalent bond5-hydroxymethylfurfuralOrganic ChemistryPhotocatalysisOrganic chemistryPartial oxidationPhysical and Theoretical ChemistryHydroxymethylfurfuralAnalytical ChemistryTriazineChemPhotoChem
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Structural insight on organosilica electrodes for waste-free alcohol oxidations

2007

Organic modification of sol-gel catalytic glassy electrodes made of a thin layer of organosilica doped with nitroxyl radical TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy) crucially enhances stability in the waste-free oxidation of alcohols to carbonyls in water. Structural comparison between analogous films made of organosilica and unmodified SiO2 shows that the origin of the pronounced stable activity of the ORMOSIL film lies in high hydrophobic and also in the pronounced low degree of hydrophilicity.

Green chemistryoxidationalcoholgreen chemistryInorganic chemistryAlcoholNitroxylGeneral ChemistryPhotochemistryHeterogeneous catalysisOrmosilCatalysisCatalysischemistry.chemical_compoundchemistryAlcohol oxidationsol-gelanodicTEMPOSol-gel
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Mechanically-biologically treated municipal solid waste as a support medium for microbial methane oxidation to mitigate landfill greenhouse emissions.

2005

The residual fraction of mechanically-biologically treated municipal solid waste (MBT residual) was studied in the laboratory to evaluate its suitability and environmental compatibility as a support medium in methane (CH(4)) oxidative biocovers for the mitigation of greenhouse gas emissions from landfills. Two MBT residuals with 5 and 12 months total (aerobic) biological stabilisation times were used in the study. MBT residual appeared to be a favourable medium for CH(4) oxidation as indicated by its area-based CH(4) oxidation rates (12.2-82.3 g CH(4) m(-2) d(-1) at 2-25 degrees C; determined in CH(4)-sparged columns). The CH(4) oxidation potential (determined in batch assays) of the MBT re…

Greenhouse EffectConservation of Natural ResourcesMunicipal solid wasteWaste managementchemistry.chemical_elementNitrous oxideMethaneRefuse Disposalchemistry.chemical_compoundBioreactorschemistryGreenhouse gasEnvironmental chemistryAnaerobic oxidation of methaneSoil waterLeachateCitiesWaste Management and DisposalMethaneOxidation-ReductionArsenicWater Pollutants ChemicalWaste management (New York, N.Y.)
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