Search results for "METHANE"

showing 10 items of 1763 documents

Screening of ceria-based catalysts for internal methane reforming in low temperature SOFC

2010

Gaudillere, Cyril Vernoux, Philippe Mirodatos, Claude Caboche, Gilles Farrusseng, David 6th World Congress on Oxidation Catalysis (6WCOC) JUL 05-10, 2009 Lille, FRANCE; International audience; Ceria-based catalysts have been assessed for internal methane reforming at low temperature (400-600 C) in Solid Oxide Fuel Cell (SOFC) A combinatorial library of 15 metal (Cu Pt Ni) supported ceria was prepared using wet impregnation method The ceria-based oxides are undoped or doped with metal transition (Zr) or by rare earth (Gd or Pr) The effect of the metal the dopant and the surface area on the catalytic performances was investigated in high-throughput manner using a 16-parallel reactor The catal…

Cerium oxideMethane reformerDopantChemistryInorganic chemistry02 engineering and technologyGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistry021001 nanoscience & nanotechnologyHeterogeneous catalysis01 natural sciences[SDE.ES]Environmental Sciences/Environmental and SocietyCatalysisMethane0104 chemical sciencesCatalysischemistry.chemical_compoundCatalytic reforming13. Climate actionSolid oxide fuel cell0210 nano-technology
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Martian zeolites as a source of atmospheric methane

2016

The origin of the martian methane is still poorly understood. A plausible explanation is that methane could have been produced either by hydrothermal alteration of basaltic crust or by serpentinization of ultramafic rocks producing hydrogen and reducing crustal carbon into methane. Once formed, methane storage on Mars is commonly associated with the presence of hidden clathrate reservoirs. Here, we alternatively suggest that chabazite and clinoptilolite, which belong to the family of zeolites, may form a plausible storage reservoir of methane in the martian subsurface. Because of the existence of many volcanic terrains, zeolites are expected to be widespread on Mars and their Global Equival…

Chabazite010504 meteorology & atmospheric sciencesClathrate hydrateFOS: Physical sciences01 natural sciencesMethaneAstrobiologychemistry.chemical_compound0103 physical sciences010303 astronomy & astrophysicsComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesEarth and Planetary Astrophysics (astro-ph.EP)BasaltMartianAtmospheric methaneAstronomy and AstrophysicsMars Exploration ProgramAtmosphere of Marschemistry13. Climate actionSpace and Planetary Science[SDU]Sciences of the Universe [physics]Environmental science[PHYS.ASTR]Physics [physics]/Astrophysics [astro-ph][ SDU ] Sciences of the Universe [physics]Astrophysics - Earth and Planetary Astrophysics
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ZrO2 Acting as a Redox Catalyst

2016

Surface defects are discussed and reviewed with regards to the use of ZrO2 in applications involving interactions with CO, H2, CH4, CO2, water and hydrocarbons. Studies of catalytic partial oxidation of methane reveal that part of the surface lattice oxygen in terraces can be removed by methane at high temperatures (e.g. 900 °C). The reaction proceeds via a surface confined redox mechanism. The studies presented here also highlight that defects play a decisive role in the water–gas-shift reaction, since the reaction is likely carried out via OH groups present at defect sites, which are regenerated by dissociating water. Hydroxyl chemistry on ZrO2 is briefly reviewed related to the studies p…

Chemistry(all)Tar oxidationInorganic chemistryHydroxyl groups02 engineering and technology010402 general chemistry01 natural sciencesRedoxCatalysisMethaneDissociation (chemistry)CatalysisRedoxHSchemistry.chemical_compoundAdsorptionZrO2Partial oxidationbiologyH2SCPOMActive siteGeneral ChemistryZrO021001 nanoscience & nanotechnology0104 chemical scienceschemistrybiology.proteinDensity functional theory0210 nano-technologyWGSTopics in Catalysis
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Anaerobic removal of 1-methoxy-2-propanol under ambient temperature in an EGSB reactor

2015

Two laboratory-scale expanded granular sludge bed (EGSB) reactors were operated at 18 and 25 °C, respectively, for the treatment of synthetic wastewater composed of ethanol and 1-methoxy-2-propanol (M2P) in a mass ratio of 4:1. Reactors were operated first with continuous wastewater supply and after with discontinuous substrate supply (5 days a week, 16 h a day) to simulate shift working conditions. Under continuous wastewater supply chemical oxygen demand (COD), removal efficiency higher than 95 % was achieved at the end of the trial applying organic loading rates (OLR) of 29 and 43 kg COD m(-3) day(-1) at 18 and 25 °C; thus, corresponding to M2P OLR of 6.4 and 9.3 kg COD m(-3) day(-1), re…

ChemistryChemical oxygen demandEnvironmental engineeringSubstrate (chemistry)BioengineeringPortable water purificationGeneral MedicineQuímicaWastewaterPulp and paper industryMethaneWater PurificationPropanolchemistry.chemical_compoundBioreactorsWastewaterPropylene GlycolsBioreactorSewage treatmentAnaerobiosisBiotechnology
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Dimeric resorcinarene salt capsules with very tight encapsulation of anions and guest molecules

2015

Crystallization of N-cyclohexyl ammonium resorcinarene triflate from methanol results in a dimeric capsule capable of trapping two triflate anions and two methanol molecules within a 341 A3 cavity while with 1,4-dioxane as a guest it forms a new larger dimeric capsule with volume of 679 A3 encapsulating four 1,4-dioxane and four water molecules, resulting in packing coefficients of 0.75 and 0.67, respectively.

ChemistryGeneral Chemical EngineeringInorganic chemistrydimeric capsulesGeneral ChemistryResorcinarenelaw.inventionguest moleculeschemistry.chemical_compoundlawPolymer chemistryMoleculeMethanolCrystallizationta116anionsTrifluoromethanesulfonateRSC Advances
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Asymmetric Hydrogenation of Nonfunctionalized Olefins in Propylene Carbonate—Kinetic or Thermodynamic Control?

2011

Iridium-catalyzed hydrogenations of nonfunctionalized olefins in propylene carbonate as the solvent allow efficient catalysis with much higher enantioselectivities in comparison with dichloromethane which is usually employed for these reactions. Experimental and computational studies of the hydrogenation of 1-methylene-1,2,3,4-tetrahydronaphthalene have been performed to understand the limitation for this reaction.

ChemistryGeneral Chemical EngineeringKineticsInorganic chemistryAsymmetric hydrogenationGeneral ChemistryKinetic energyIndustrial and Manufacturing EngineeringCatalysisSolventchemistry.chemical_compoundPropylene carbonateOrganic chemistryDichloromethaneIndustrial & Engineering Chemistry Research
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cis-Aquabis[bis(diphenylphosphino)ethane-κ2 P,P′]chlororuthenium(II) hexafluorophosphate dichloromethane sesquisolvate hemihydrate

2006

In the title compound, [RuCl(C26H24P)2(H2O)]PF6·1.5CH2Cl2·0.5H2O, the complex RuII cation is in a slightly distorted octahedral environment, chelated by two bis(diphenylphosphino)ethane ligands, with a water molecule and a chloride anion in a mutually cis geometry completing the coordination.

ChemistryHemihydratechemistry.chemical_elementGeneral ChemistryCondensed Matter PhysicsHEXAPhosphateMedicinal chemistryChlorideMethaneRutheniumchemistry.chemical_compoundmedicineOrganic chemistryGeneral Materials ScienceChelationmedicine.drugActa Crystallographica Section E Structure Reports Online
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An ab Initio MO Study of Silver Triflate Complexation in [2.2.1]Cyclophane π-Prismands

2002

Ab initio Hartree-Fock and DFT MO calculations have been used to study the conformations of six [2.2.1]cyclophane π-prismands and the formation of their π-complexes with silver triflate (AgSO 3 CF 3 ). The lowest energy cyclophane conformations and their silver triflate π-complexes have been calculated with HF/3-21G* and B3LYP/3-21G* levels of theory. The nature of bonding in silver triflate π-complexes has been studied with natural bond orbital analysis (NBO). Energies of the calculated cyclophanes and complexes, together with the formation energies of those complexes, have also been discussed. The results have been compared to available X-ray crystal structures and also to results of the …

ChemistryHydrogen bondLigandOrganic ChemistryAb initioPhotochemistryIonInorganic ChemistryCrystallographychemistry.chemical_compoundAb initio quantum chemistry methodsPhysical and Theoretical ChemistryTrifluoromethanesulfonateCyclophaneNatural bond orbitalOrganometallics
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Binding Modes of Nonspherical Anions to N-Alkylammonium Resorcinarenes in the Solid State

2012

A series of hydrogen bond stabilized N-alkylammonium resorcinarene salts with nitrate, triflate, and picrate as the counteranions were synthesized and characterized with 1H NMR and electrospray ionization (ESI) mass spectrometry. Together with electrostatic interactions, the binding of the anions with several hydrogen bond donor sites proceeds through a complex array of intra- and intermolecular hydrogen bonds, evidenced by single crystal X-ray diffraction analysis. These N-alkyl ammonium resorcinarenes bind the larger nonspherical anions into deformed cavitand-like structures and enforce a transformation of the resorcinarene conformation from almost symmetrical to extremely distorted.

ChemistryHydrogen bondPicrateElectrospray ionizationIntermolecular forceInorganic chemistryGeneral ChemistryResorcinareneCondensed Matter PhysicsMass spectrometrychemistry.chemical_compoundCrystallographyProton NMRGeneral Materials ScienceTrifluoromethanesulfonateta116resorcinarenes; non-spherical anions; hydrogen bonding; X-ray structureCRYSTAL CROWTH & DESIGN
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ChemInform Abstract: THE PREPARATION OF DIHYDROXYDIPHENYLMETHANE DERIVATIVES CONTAINING NITRO GROUPS PART 1, SYMMETRICALLY SUBSTITUTED COMPOUNDS

1974

(1974). THE PREPARATION OF DIHYDROXYDIPHENYLMETHANE DERIVATIVES CONTAINING NITRO GROUPS. I. SYMMETRICALLY SUBSTITUTED COMPOUNDS. Organic Preparations and Procedures International: Vol. 6, No. 3, pp. 123-130.

ChemistryNitroGeneral MedicineMedicinal chemistryDiphenylmethane derivativesChemischer Informationsdienst
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