Search results for "METHANE"

showing 10 items of 1763 documents

Oxidative dehydrogenation of ethane: A study over the structure and robustness of Ni–W–O catalysts

2014

[EN] The robustness of one selected Ni-W-O catalyst has been studied in the oxidative dehydrogenation of ethane. This catalyst initially deactivates for the first 10 h online decreasing 15% of its catalytic activity compared to its initial stable catalytic activity. However from 10 to 60 h online the catalytic activity keeps almost stable. On the other hand, it has been shown that the Ni-W-O catalyst cannot tolerate an oxygen-free atmosphere (C-2 and He) as nickel oxide is transformed into metallic nickel. Methane and hydrogen as well as abundant coke were formed on the surface of the catalyst in these O-free conditions. However a re-calcination in air leads to the removal of coke, the cata…

inorganic chemicalsEthyleneHydrogenGeneral Chemical EngineeringCatalyst supportInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCatalysisMethaneCatalysisEthylenechemistry.chemical_compoundDehydrogenationNickel tungstenOxidative dehydrogenation of ethaneOxide catalystsEthaneChemistryorganic chemicalsNickel oxideCokeFuel TechnologyNi-W-OHydrogenOxidative dehydrogenationFuel Processing Technology
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Highly Active Co3O4-Based Catalysts for Total Oxidation of Light C1–C3 Alkanes Prepared by a Simple Soft Chemistry Method: Effect of the Heat-T…

2021

9 figures, 2 tables.

inorganic chemicalsTechnologyInorganic chemistryTotal oxidationcobalt oxidechemistry.chemical_elementalkane oxidationpropaneHeterogeneous catalysissurface oxygen vacanciesMethaneArticleCatalysischemistry.chemical_compoundPropaneAlkane oxidationSurface oxygen vacanciesPropanetotal oxidationvolatile organic compoundsGeneral Materials ScienceReactivity (chemistry)Volatile organic compoundsCobalt oxideAlkanechemistry.chemical_classificationHeterogeneous catalysisEthaneMicroscopyQC120-168.85methaneTQH201-278.5ethaneEngineering (General). Civil engineering (General)TK1-9971heterogeneous catalysischemistryDescriptive and experimental mechanicsMixed oxideElectrical engineering. Electronics. Nuclear engineeringTA1-2040cobalt oxide; total oxidation; alkane oxidation; heterogeneous catalysis; volatile organic compounds; propane; ethane; methane; surface oxygen vacanciesCobaltMethaneMaterials; Volume 14; Issue 23; Pages: 7120
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Thieme Chemistry Journals Awardees – Where Are They Now? Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

2017

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

inorganic chemicalschemistry.chemical_classificationmolybdenum pentachloridedisulfides010405 organic chemistryArylOrganic Chemistrychemistry.chemical_elementMolybdenum pentachloride010402 general chemistryoxidative coupling01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMolybdenumReagentcross-couplingOrganic chemistryOxidative coupling of methaneC–S bond formationAlkylSynlett
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Benzen i metan jako wzorce przesunięcia chemicznego 1 H i 13 C NMR w obliczeniach teoretycznych

2020

NMR spectroscopy belongs to the most versatile techniques used in chemical laboratory for testing the presence of various compounds and elucidation of their structure. In case of more complex natural products chemical intuition and experience applied to analysis of experimental spectra is often supported by theoretical modeling of NMR spectra. However, theoretical predictions should be reliable and the errors associated with the approximations inherent to the existing methods minimized. In this respect, systematic errors, present in calculation of isotropic nuclear magnetic shieldings of the studied molecule need to be minimized. Conversion of nuclear shieldings of the studied molecule to t…

izoprenbenzenetensor ekranowania magnetycznegocytozynabenzenwzorce przesunięcia chemicznegomethanecytosineisoprenemetannuclear magnetic shielding tensorchemical shift referencesWiadomości Chemiczne
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Pt(II) and Pd(II)-assisted coupling of nitriles and 1,3-diiminoisoindoline : Synthesis and luminescence properties of (1,3,5,7,9-pentaazanona-1,3,6,8…

2017

Treatment of trans-[PtCl2(NCR)2] 1 (R = Me (1a), Et (1b), o-ClC6H4 (1c), p-ClC6H4 (1d), p-(HCdouble bond; length as m-dashO)C6H4 (1e), p-O2NC6H4CH2 (1f)) with 1,3-diiminoisoindoline HNdouble bond; length as m-dashCC6H4C(NH)double bond; length as m-dashNH 2 gives access to the corresponding (1,3,5,7,9-pentaazanona-1,3,6,8-tetraenato)Pt(II) complexes [PtCl{NHdouble bond; length as m-dashC(R)Ndouble bond; length as m-dashC(C6H4)NCdouble bond; length as m-dashNC(R)double bond; length as m-dashNH}] 3a–f, in good yields (65–70%). The reaction of trans-[PdCl2(NCMe)2] 4a with 2 furnishes (1,3,5,7,9-pentaazanona-1,3,6,8-tetraenato)Pd(II) complex [PdCl{NHdouble bond; length as m-dashC(Me)Ndouble bond…

kemiaStereochemistryhiili1Solid-state010402 general chemistrychemistry01 natural sciencesMedicinal chemistrynitrogenInorganic Chemistrychemistry.chemical_compoundpentaazanonatetraene complexestyppiMaterials ChemistryluminescencenitrilesPhysical and Theoretical Chemistryta116Dichloromethanemetal-assisted additions010405 organic chemistryluminesenssicarbonCoupling (probability)0104 chemical scienceschemistryYield (chemistry)13-diiminoisoindolinePolystyreneAbsorption (chemistry)Luminescence3-diiminoisoindolinePolyhedron
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Global analysis of the high resolution infrared spectrum of methane 12CH4 in the region from 0 to 4800 cm-1

2009

International audience; We report the global analysis of methane (12CH4) lines from high resolution rovibrational spectra including accurate line positions and intensities in the region 0–4800 cm−1. This covers four polyads: The Ground State Monad (rotational levels), the Dyad (940–1850 cm−1, 2 vibrational levels, 2 sublevels), the Pentad (2150–3350 cm−1, 5 vibrational levels, 9 sublevels) and the Octad (3550–4800 cm−1, 8 vibrational levels, 24 sublevels) and some of the associated hot bands (Pentad−Dyad and Octad−Dyad). New Fourier transform infrared (FTIR) spectra of the Pentad and Octad regions have been recorded with a very high resolution (better than 0.001 cm−1 instrumental bandwidth,…

line intensitiesInfraredGeneral Physics and Astronomy02 engineering and technology01 natural sciencesSpectral lineRoot mean squaresymbols.namesakehigh resolution infrared spectra0103 physical sciencesPhysical and Theoretical Chemistry[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]010304 chemical physicsSpectrometerChemistryRotational–vibrational spectroscopy021001 nanoscience & nanotechnologyPotential energyFourier transform[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]symbolsrovibrational analysisAtomic physics0210 nano-technologyGround stateMethanevibrational states
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Preliminary analysis of CH3D from 3250 to 3700 cm(-1)

2006

International audience; The infrared spectrum of CH3D from 3250 to 3700 cm(-1) was studied for the first time to assign transitions involving the nu(2) + nu(3), nu(2) + nu(5), nu(2) + nu(6), nu(3) + 2(nu 6) and 3 nu(6) vibrational states. Line positions and intensities were measured at 0.011 cm(-1) resolution using Fourier transform spectra recorded at Kitt Peak with isotopically enriched samples. Some 2852 line positions (involving over 900 upper state levels) and 874 line intensities were reproduced with RMS values of 0.0009 cm(-1) and 4.6%, respectively. The strongest bands were found to be nu(2) + nu(3) at 3499.7 cm(-1) and nu(2) + nu(6) at 3342.5 cm(-1) with integrated strengths, respe…

line intensitieshot bands010504 meteorology & atmospheric sciencesInfraredmonodeuterated methaneFourier transform spectra01 natural sciencesPreliminary analysisRoot mean squaresymbols.namesake0103 physical sciencesline positionsPhysical and Theoretical Chemistry010303 astronomy & astrophysicsSpectroscopydatabase0105 earth and related environmental sciences[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Physics33.20.EaAtomic and Molecular Physics and OpticsCH3D[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph][ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]symbols[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Atomic physicsGround stateHamiltonian (quantum mechanics)
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Room-Temperature Magnetic Bistability in a Salt of Organic Radical Ions

2021

International audience; Cocrystallization of 7,7′,8,8′-tetracyanoquinodimethane radical anion (TCNQ −•) and 3-methylpyridinium-1,2,3,5dithiadiazolyl radical cation (3-MepyDTDA +•) afforded isostructural acetonitrile (MeCN) or propionitrile (EtCN) solvates containing cofacial π dimers of homologous components. Loss of lattice solvent from the diamagnetic solvates above 366 K affords a high-temperature paramagnetic phase containing discrete TCNQ −• and weakly bound π dimers of 3-MepyDTDA +• , as evidenced by X-ray diffraction methods and magnetic susceptibility measurements. Below 268 K, a first-order phase transition occurs, leading to a low-temperature diamagnetic phase with TCNQ −• σ dimer…

magneettiset ominaisuudetDimer02 engineering and technologyGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistry010402 general chemistry021001 nanoscience & nanotechnologyvapaat radikaalit01 natural sciencesBiochemistryTetracyanoquinodimethaneMagnetic susceptibilityCatalysis0104 chemical scienceschemistry.chemical_compoundParamagnetismCrystallographyColloid and Surface ChemistryRadical ionchemistryDiamagnetismPropionitrileIsostructural0210 nano-technologyorgaaniset yhdisteet
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In vivo imaging of colitis and colon cancer development in mice using high resolution chromoendoscopy

2005

Background: Mouse models of colitis and cancer are indispensable for our understanding of the pathogenesis of these diseases. In the past, mice had to be sacrificed in order to analyse colitis activity and tumour development. We have developed a safe method for high resolution endoscopic monitoring of living mice. Methods: Mice developing colitis or colonic tumours were anaesthetised using avertine and repeatedly examined by endoscopy. A novel miniendoscope (1.9 mm outer diameter), denoted Coloview, was introduced via the anus and the colon was carefully insufflated with an air pump before analysis of the colonic mucosa. An extra working channel allowed the introduction of biopsy forceps or…

medicine.medical_specialtyPathologyColorectal cancerAzoxymethaneColonoscopyMice Inbred StrainsSeverity of Illness IndexGastroenterologyChromoendoscopyMiceIntestinal mucosaInternal medicineBiopsymedicineAnimalsIntestinal MucosaColitisGrading (tumors)Colonoscopesmedicine.diagnostic_testbusiness.industryDextran SulfateInflammatory Bowel DiseaseGastroenterologyCancerColonoscopyColitismedicine.diseaseDisease Models AnimalCell Transformation NeoplasticColonic NeoplasmsDisease ProgressionbusinessGut
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Stability of Cannabinoids in Hair Samples Exposed to Sunlight

2000

It has been well recognized that hashish and marihuana lose potency during storage because of a decrease in the content of tetrahydrocannabinol (THC), which is the major psychoactive constituent of cannabis (1). The effect of oxygen on stored plant and resin materials or solutions of pure cannabinoids seems much less significant than that of higher temperatures (≥37 °C) or light (2)(3)(4)(5)(6)(7). A few data are available on the stability of THC and major metabolites in blood (8)(9)(10)(11). However, the stability of cannabinoids in the hair shaft has not been addressed, although scalp hair represents one of the most exposed parts of the body. Therefore, a study was performed to elucidate …

medicine.medical_treatmentClinical BiochemistryCannabinolAnalytical chemistryHashishSpecimen HandlingMatrix (chemical analysis)chemistry.chemical_compoundmedicineCannabidiolHumansDronabinolTetrahydrocannabinolDichloromethaneChromatographybiologyCannabinoidsBiochemistry (medical)biology.organism_classificationSubstance Abuse DetectionchemistrySunlightCannabinolCannabinoidCannabisCannabidiolHairmedicine.drugClinical Chemistry
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