Search results for "METHANE"

showing 10 items of 1763 documents

Synthesis and support composition effects on CH4 partial oxidation over Ni–CeLa oxides

2015

Abstract Two series of Ni (6 wt%) catalysts supported over CeO 2 , La 2 O 3 and mixed CeO 2 –La 2 O 3 were prepared by co-precipitation and by wet-impregnation. The effect of the two Ni loading procedures on the catalyst structural properties was investigated by XRD, TPR and XPS. The catalytic behavior of the catalysts was tested in the methane partial oxidation reaction performed at 1 atm in a temperature range of 400–800 °C using dilute feed gas mixture with CH 4 /O 2  = 2 and gas hourly space velocity of 60,000 ml g −1  h −1 . Total methane combustion was observed within the 450 °C ≤  T ≤ 650 °C temperature range. Above 650 °C partial oxidation of methane started to occur, reaching at 80…

Process Chemistry and TechnologyInorganic chemistryOxidechemistry.chemical_elementAtmospheric temperature rangeCatalysisMethaneCatalysisNickelchemistry.chemical_compoundchemistryLanthanumPartial oxidationGeneral Environmental ScienceSpace velocityApplied Catalysis B: Environmental
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Combined CO/CH4 oxidation tests over Pd/Co3O4 monolitic catalyst: effects of high reaction temperature and SO2 exposure on the deactivation process

2007

Abstract CO and CH 4 combined oxidation tests were performed over a Pd (70 g/ft 3 )/Co 3 O 4 monolithic catalyst in conditions of GHSV = 100,000 h −1 and feed composition close to that of emission from bi-fuel vehicles. The effect of SO 2 (5 ppm) on CO and CH 4 oxidation activity under lean condition ( λ  = 2) was investigated. The presence of sulphur strongly deactivated the catalyst towards methane oxidation, while the poisoning effect was less drastic in the oxidation of CO. Saturation of the Pd/Co 3 O 4 catalytic sites via chemisorbed SO 3 and/or sulphates occurred upon exposure to SO 2 . A treatment of regeneration to remove sulphate species was attempted by performing a heating/coolin…

Process Chemistry and TechnologyInorganic chemistrySinteringHeterogeneous catalysisDecompositionCatalysisMethaneCatalysischemistry.chemical_compoundchemistryAnaerobic oxidation of methaneOxidizing agentGeneral Environmental ScienceCarbon monoxide
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Co3O4/CeO2 composite oxides for methane emissions abatement: Relationship between Co3O4–CeO2 interaction and catalytic activity

2006

Abstract Co 3 O 4 /CeO 2 composite oxides with different cobalt loading (5, 15, 30, 50, 70 wt.% as Co 3 O 4 ) were prepared by co-precipitation method and investigated for the oxidation of methane under stoichiometric conditions. Pure oxides, Co 3 O 4 and CeO 2 were used as reference. Characterization studies by X-ray diffraction (XRD), BET, temperature programmed reduction/oxidation (TPR/TPO) and X-ray photoelectron spectroscopy (XPS) were carried out. An improvement of the catalytic activity and thermal stability of the composite oxides was observed with respect to pure Co 3 O 4 in correspondence of Co 3 O 4 –CeO 2 containing 30% by weight of Co 3 O 4 . The combined effect of cobalt oxide…

Process Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementRedoxCatalysisCatalysischemistryAnaerobic oxidation of methaneThermal stabilityTemperature-programmed reductionCobaltCobalt oxideStoichiometryGeneral Environmental ScienceApplied Catalysis B: Environmental
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Effect of ultraviolet light, methyl methanesulfonate and ionizing radiation on the genotoxic response and apoptosis of mouse fibroblasts lacking c-Fo…

2001

c-Fos and p53 are DNA damage-inducible proteins that are involved in gene regulation, cell cycle checkpoint control and cell proliferation following exposure to genotoxic agents. To investigate comparatively the role of c-Fos and p53 in the maintenance of genomic stability and the induction of apoptosis, we generated mouse fibroblast cell lines from knockout mice deficient for either c-fos (fos -/-) or p53 (p53-/-) or for both gene products (fosp53-/-). The sensitivity of these established cell lines was compared with the corresponding wild-type cells as to the cytotoxic, clastogenic and apoptosis-inducing effects of ultraviolet (UV-C) light and methyl methanesulfonate (MMS). Additionally, …

Programmed cell deathTime FactorsCell cycle checkpointCell SurvivalUltraviolet RaysHealth Toxicology and MutagenesisBlotting WesternApoptosisBiologyToxicologyPolymerase Chain ReactionCell LineMiceNecrosischemistry.chemical_compoundRadiation IonizingGeneticsUltraviolet lightAnimalsCytotoxic T cellCells CulturedGenetics (clinical)Chromosome AberrationsMice KnockoutCell growthDose-Response Relationship RadiationFibroblastsBlotting NorthernMethyl MethanesulfonateMolecular biologyMethyl methanesulfonatechemistryApoptosisCell cultureTumor Suppressor Protein p53Proto-Oncogene Proteins c-fosDNA DamageMutagensMutagenesis
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Planar Bragg Grating Sensor for the Detection of CFC-11

2018

We demonstrate the fabrication of a highly sensitive opto-chemical sensor system based on cyclodextrin derivative functionalized planar Bragg gratings for an online in-situ detection and measurement of the environmentally harmful propellant trichlorofluoromethane in real-time.

PropellantFabricationMaterials scienceTrichlorofluoromethanebusiness.industryHighly sensitivechemistry.chemical_compoundPlanarFiber Bragg gratingchemistryMoleculeOptoelectronicsbusinessSpectroscopyLight, Energy and the Environment 2018 (E2, FTS, HISE, SOLAR, SSL)
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An Organometallic Gold(I) Bis‐N‐Heterocyclic Carbene Complex with Multimodal Activity in Ovarian Cancer Cells

2020

Abstract The organometallic AuI bis‐N‐heterocyclic carbene complex [Au(9‐methylcaffeine‐8‐ylidene)2]+ (AuTMX2) was previously shown to selectively and potently stabilise telomeric DNA G‐quadruplex (G4) structures. This study sheds light on the molecular reactivity and mode of action of AuTMX2 in the cellular context using mass spectrometry‐based methods, including shotgun proteomics in A2780 ovarian cancer cells. In contrast to other metal‐based anticancer agents, this organogold compound is less prone to form coordinative bonds with biological nucleophiles and is expected to exert its drug effects mainly by non‐covalent interactions. Global protein expression changes of treated cancer cell…

ProteomicsNucleolusCancer | Very Important PaperContext (language use)Antineoplastic Agents010402 general chemistryProteomicsG-quadruplex01 natural sciencesCatalysischemistry.chemical_compoundgold complexesCaffeineCell Line TumorOrganometallic CompoundscancerHumansN-heterocyclic carbenesShotgun proteomicsMode of actionOvarian NeoplasmsFull Paper010405 organic chemistryChemistryOrganic ChemistryGeneral ChemistryFull PaperstelomeresG-quadruplexes0104 chemical sciencesddc:BiochemistryCancer cellFemaleGoldCarbeneMethane
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Influence of structure on the polarizability of hydrated methane sulfonic acid clusters

2015

Abstract: The relationship between polarizability and structure is investigated in methane sulfonic acid (MSA) and in 36 hydrated MSA clusters. The polarizabilities are calculated at B3LYP and MP2 level and further partitioned into molecular contributions using classic and iterative Hirshfeld methods. The differences in the two approaches for partitioning of polarizabilities are thoroughly analyzed. The polarizabilities of the molecules are found to be influenced in a systematic way by the hydrogen bond network in the clusters, proton transfer between MSA and water molecules, and weak interactions between water molecules and the methyl group of MSA.

ProtonChemistryHydrogen bondPhysicsQuantitative Biology::GenomicsComputer Science Applicationschemistry.chemical_compoundQuantitative Biology::Quantitative MethodsChemistryComputational chemistryPolarizabilityMethane sulfonic acidPhysics::Atomic and Molecular ClustersMoleculePhysics::Atomic PhysicsPhysical and Theoretical ChemistryPhysics::Chemical PhysicsMethyl groupJournal of chemical theory and computation
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Is the repair of oxidative DNA base modifications inducible by a preceding DNA damage induction?

2007

In mammalian cells, 7,8-dihydro-8-oxoguanine (8-oxoG) and some other oxidative guanine modifications are removed from the DNA by base excision repair, which is initiated by OGG1 protein. We have tested whether this repair is inducible in mouse embryonic fibroblasts (MEFs), MCF-7 breast cancer cells and primary human fibroblasts by a pretreatment with the photosensitizer Ro19-8022 plus light, which generates predominantly 8-oxoG, or with methyl methanesulfonate (MMS), which generates alkylated bases and abasic sites (AP sites). The results indicate that the repair rate of the oxidative guanine modifications induced by the photosensitizer was not increased if a priming dose of the oxidative o…

PyrrolidinesTime FactorsDNA RepairDNA repairGuanineDNA damageBiologymedicine.disease_causeBiochemistryMicechemistry.chemical_compoundTumor Cells CulturedmedicineAnimalsHumansheterocyclic compoundsAntineoplastic Agents AlkylatingBase PairingMolecular BiologyPhotosensitizing AgentsGuanosineDNACell BiologyBase excision repairGlutathioneFibroblastsMethyl MethanesulfonateGlutathioneMolecular biologyMethyl methanesulfonateOxidative StresschemistryFemaleOxidation-ReductionQuinolizinesDNAOxidative stressDNA DamageDNA Repair
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Modeling of anaerobic degradation of solid slaughterhouse waste: inhibition effects of long-chain fatty acids or ammonia.

2003

The anaerobic bioconversion of solid poultry slaughterhouse wastes was kinetically investigated. The modified version ofMETHANEsimulation model was applied for description of experimental data in mesophilic laboratory digester and assays. Additionally, stages of formation and consumption of long chain fatty acids (LCFA) were included in the model. Batch data on volatile solids, ammonium, acetate, butyrate, propionate, LCFA concentrations, pH level, cumulative volume, and methane partial pressure were used for model calibration. As a reference, the model was used to describe digestion of solid sorted household waste. Simulation results showed that an inhibition of polymer hydrolysis by volat…

Quality ControlBioconversionCell Culture TechniquesIndustrial WasteBioengineeringApplied Microbiology and BiotechnologyBiochemistryModels BiologicalIndustrial wasteHydrolysisBacteria AnaerobicBioreactorsAmmoniaBioreactorComputer SimulationMolecular Biologychemistry.chemical_classificationChromatographySewageChemistryGeneral MedicineBiodegradationRefuse DisposalAnaerobic digestionBiodegradation EnvironmentalBiochemistryAcetogenesisPropionateFatty Acids Unsaturatedlipids (amino acids peptides and proteins)MethaneAbattoirsCell DivisionBiotechnologyApplied biochemistry and biotechnology
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Ab Initio Modeling of Donor–Acceptor Interactions and Charge-Transfer Excitations in Molecular Complexes: The Case of Terthiophene–Tetracyanoquinodim…

2015

This work presents a thorough quantum chemical study of the terthiophene-tetracyanoquinodimethane complex as a model for π-π donor-acceptor systems. Dispersion-corrected hybrid (B3LYP-D) and double hybrid (B2PLYP-D), hybrid meta (M06-2X and M06-HF), and recently proposed long-range corrected (LC-wPBE, CAM-B3LYP, and wB97X-D) functionals have been chosen to deal with π-π intermolecular interactions and charge-transfer excitations in a balanced way. These properties are exhaustively compared to those computed with high-level ab initio SCS-MP2 and CASPT2 methods. The wB97X-D functional exhibits the best performance. It provides reliable intermolecular distances and interaction energies and pre…

Quantum chemicalChemistryAb initioCharge (physics)computer.software_genreTetracyanoquinodimethaneComputer Science Applicationschemistry.chemical_compoundTerthiopheneChemical physicsData miningPhysical and Theoretical ChemistryDonor acceptorcomputerJournal of Chemical Theory and Computation
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