Search results for " methane"

showing 10 items of 146 documents

Near-infrared radiative transfer modelling with different CH4 spectroscopic databases to retrieve atmospheric methane total amount

2011

International audience; Atmospheric methane content can be retrieved from measurements of solar radiation attenuated by the atmosphere in the near infrared spectral region where the space-borne and ground-based spectrometers carry out regular measurements. It is shown, in the present work, that the different spectroscopic databases can give significantly different results for both forward simulations of the atmospheric transmittance and the inverse problem solution to retrieve the CH4 total content in the atmosphere using spectra measured by ground-based FTIR spectrometer in the near infrared spectral region. These discrepancies and the problem of the reduction of their influence on the atm…

Materials science010504 meteorology & atmospheric sciencesInfrared spectroscopycomputer.software_genre01 natural sciencesAtmosphereAtmospheric radiative transfer codes0103 physical sciencesRadiative transferAstrophysics::Solar and Stellar AstrophysicsPhysics::Atmospheric and Oceanic PhysicsSpectroscopySpectroscopic databases0105 earth and related environmental sciencesRadiation010304 chemical physicsSpectrometerDatabaseAtmospheric methaneNear-infrared spectroscopyAtmospheric transmissionAtomic and Molecular Physics and Optics13. Climate actionInfrared windowAstrophysics::Earth and Planetary AstrophysicsMethanecomputerJournal of Quantitative Spectroscopy and Radiative Transfer
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Co3O4 particles grown over nanocrystalline CeO2: influence of precipitation agents and calcination temperature on the catalytic activity for methane …

2015

Crystalline cobalt oxides were prepared by a precipitation method using three different precipitation agents, (NH4)(2)CO3, Na2CO3 and CO(NH2)(2). Cobalt oxide nanoparticles corresponding to a Co3O4 loading of 30 wt% were also deposited over high-surface area nanocrystalline ceria by the same precipitation agents. The effect of calcination temperature, 350 or 650 degrees C, on the morphological and structural properties was evaluated. Characterization by BET, XRD, SEM, TEM, Raman spectroscopy, H-2-TPR, XPS and NH3-TPD was performed and the catalytic properties were explored in the methane oxidation reaction. The nature of the precipitation agent strongly influenced the textural properties of…

Materials sciencePrecipitation (chemistry)methane oxidationInorganic chemistrychemistry.chemical_elementCatalysisMethaneNanocrystalline materiallaw.inventionceriachemistry.chemical_compoundCo3O4Chemical engineeringchemistrylawCo3O4 CeO2 methane oxidationAnaerobic oxidation of methaneCalcinationCrystalliteSettore CHIM/07 - Fondamenti Chimici Delle TecnologieCobaltCobalt oxide
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Geochemistry and mineralogy of sediments and authigenic carbonates from the Malta Plateau, Strait of Sicily (Central Mediterranean): Relationships wi…

2010

Abstract A mud volcano field was recently discovered within the Malta Plateau in the Strait of Sicily (Central Mediterranean Sea). Box-core sediments and associated authigenic carbonates have been collected in water depths of 140–170 m from two distinctive sectors of the area, and analyzed for major, trace and rare earth elements, stable isotopes, and mineralogy. Relative homogeneity in the mineralogy and geochemistry of bulk sediments, and 210Pb activity distributions, argue against an active mud ejection activity. In the Malta Plateau western sector, the sediments show high concentrations of Fe, As, Sb, and Mo, exceeding the background values estimated for the Strait of Sicily. Active flu…

Methane oxidationGeochemistryMineralogyengineering.materialchemistry.chemical_compoundMediterranean seaSeep carbonateGeochemistry and PetrologygeographyPlateaugeography.geographical_feature_categoryδ13CAragoniteSediment geochemistrySettore GEO/07 - Petrologia E PetrografiaGeologyAuthigenicStable isotopeSettore GEO/08 - Geochimica E VulcanologiaStrait of SicilychemistryAnaerobic oxidation of methaneengineeringCarbonateGeologyMud volcano
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Methanotrophic activity and diversity of methanotrophs in volcanic geothermal soils at Pantelleria (Italy)

2014

Volcanic and geothermal systems emit endogenous gases by widespread degassing from soils, including CH4, a greenhouse gas twenty-five times as potent as CO2. Recently, it has been demonstrated that volcanic or geothermal soils are not only a source of methane, but are also sites of methanotrophic activity. Methanotrophs are able to consume 10–40 Tg of CH4 a−1 and to trap more than 50% of the methane degassing through the soils. We report on methane microbial oxidation in the geothermally most active site of Pantelleria (Italy), Favara Grande, whose total methane emission was previously estimated at about 2.5 Mg a−1 (t a−1). Laboratory incubation experiments with three top-soil samples from …

Methane oxidationMethane monooxygenaselcsh:LifeSettore BIO/19 - Microbiologia GeneraleMethanechemistry.chemical_compoundlcsh:QH540-549.5Soil pHEcology Evolution Behavior and SystematicsEarth-Surface ProcessesbiologyEcologylcsh:QE1-996.5bacterial diversityAlphaproteobacteriaVerrucomicrobiabiology.organism_classificationMethanotrophSettore GEO/08 - Geochimica E Vulcanologialcsh:Geologylcsh:QH501-531chemistryEnvironmental chemistryMethane emissionAnaerobic oxidation of methaneSoil waterbiology.proteinSoil horizonlcsh:EcologyBiogeosciences
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Group-specific quantification of methanotrophs in landfill gas-purged laboratory biofilters by tyramide signal amplification-fluorescence in situ hyb…

2008

The aim of this study was to quantitatively analyse methanotrophs in two laboratory landfill biofilters at different biofilter depths and at temperatures which mimicked the boreal climatic conditions. Both biofilters were dominated by type I methanotrophs. The biofilter depth profiles showed that type I methanotrophs occurred in the upper layer, where relatively high O(2) and low CH(4) concentrations were present, whereas type II methanotrophs were mostly distributed in the zone with high CH(4) and low O(2) concentrations. The number of type I methanotrophic cells declined when the temperature was raised from 15 degrees C to 23 degrees C, but increased when lowered to 5 degrees C. A slight …

MethanobacteriaceaeEnvironmental EngineeringType I methanotrophsBioengineeringmedicineWaste Management and DisposalIn Situ Hybridization FluorescenceDNA PrimersType II methanotrophsmedicine.diagnostic_testBase SequenceRenewable Energy Sustainability and the EnvironmentChemistryEnvironmental engineeringGeneral MedicineAmidesRefuse DisposalLandfill gasEnvironmental chemistrySoil waterAnaerobic oxidation of methaneBiofilterGasesOligonucleotide ProbesSignal amplificationFiltrationFluorescence in situ hybridizationBioresource technology
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2015

Iron reduction in subseafloor sulfate-depleted and methane-rich marine sediments is currently a subject of interest in subsurface geomicrobiology. While iron reduction and microorganisms involved have been well studied in marine surface sediments, little is known about microorganisms responsible for iron reduction in deep methanic sediments. Here, we used quantitative PCR (Q-PCR)-based 16S rRNA gene copy numbers and pyrosequencing-based relative abundances of bacteria and archaea to investigate covariance between distinct microbial populations and specific geochemical profiles in the top 5 m of sediment cores from the Helgoland mud area, North Sea. We found that gene copy numbers of bacteri…

Microbiology (medical)EcologyGeomicrobiologyMicroorganismSediment15. Life on landBiologybiology.organism_classificationMicrobiologyMethanohalobium13. Climate actionAnaerobic oxidation of methaneDesulfobacteraceae14. Life underwaterMethanosaetaceaeArchaeaFrontiers in Microbiology
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Synthesis of highly functionalized 9,10-phenanthrenequinones by oxidative coupling using MoCl5.

2012

The strong oxidative power of molybdenum pentachloride gives rise to an efficient oxidative C-C bond formation of benzil derivatives to the corresponding 9,10-phenanthrenequinones. A highly complementary method to previous approaches was developed. The required derivatives are accessible in a modular fashion and in excellent yields. By this approach the orchid-derived natural product cypripediquinone A was synthesized for the first time.

Models MolecularMolybdenumNatural productMolecular StructureOxidative CouplingOrganic ChemistryBond formationMolybdenum pentachloridePhenanthrenesPhotochemistryBiochemistryCombinatorial chemistrychemistry.chemical_compoundchemistryChloridesMoleculeOxidative coupling of methaneBenzilPhysical and Theoretical ChemistryOrganic letters
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Synthesis and application of β-substituted Pauson-Khand adducts: trifluoromethyl as a removable steering group.

2013

The reaction between alkynes (I) and norbornadiene (II) affords the β-substituted Pauson—Khand adducts (III) as single regioisomers and the trifluoromethyl steering group can be easily removed in the presence of DBU and water.

Models MolecularTrifluoromethylMolecular StructureChemistryNorbornadienePauson–Khand reactionRegioselectivityStereoisomerismGeneral MedicineGeneral ChemistryChemistry Techniques SyntheticCatalysisAdductchemistry.chemical_compoundAlkynesStructural isomerOrganic chemistryPolycyclic CompoundsSteering groupMicrowavesSesquiterpenesChlorofluorocarbons MethaneAngewandte Chemie (International ed. in English)
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Novel Domino Oxidative Coupling: C−C Bond Formation Sequence to Highly Functionalized Dibenzo[a,c]cycloheptenes

2011

A domino sequence involving various MoCl(5)-mediated oxidations followed by trapping and supposed [3,3]-sigmatropic rearrangement provides a fast access to the full carbon skeleton of metasequirin-B. A variety of different moieties R(1) and R(2) are tolerated.

MolybdenumMolecular StructureOxidative CouplingChemistryStereochemistryOrganic ChemistryCarbon skeletonSequence (biology)DibenzocycloheptenesBond formationBiochemistryCatalysisLignansDominoChloridesCyclizationBenzene DerivativesOxidative coupling of methanePhysical and Theoretical ChemistryOxidation-ReductionOrganic Letters
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Oxidative cyclization reaction of 2-aryl-substituted cinnamates to form phenanthrene carboxylates by using MoCl5.

2014

The oxidative cyclization reaction of 2-aryl cinnamates and derivatives thereof can be easily performed with MoCl5 as the oxidant. This powerful reagent allows oxidative coupling reactions for which other reagents fail. The best results are obtained when the 2-phenyl substituent of the cinnamate is equipped with two methoxy groups. Even iodo moieties in the bay region of phenanthrene are tolerated under the reaction conditions. If naphthalene moieties are involved, a rearrangement of the skeleton occurs, providing an elegant route to highly functionalized angular arenes. The cyclization is demonstrated for 15 example substrates with isolated yields of up to 99 % for the phenanthrene derivat…

MolybdenumOxidative cyclizationArylOrganic ChemistrySubstituentCarboxylic AcidsGeneral ChemistryPhenanthrenePhenanthrenesMedicinal chemistryCatalysischemistry.chemical_compoundchemistryChloridesCinnamatesCyclizationReagentCinnamatesOrganic chemistryOxidative coupling of methaneOxidation-ReductionNaphthaleneChemistry (Weinheim an der Bergstrasse, Germany)
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