Search results for "GAS-PHASE"

showing 10 items of 12 documents

Computational determination of the dominant triplet population mechanism in photoexcited benzophenone

2014

In benzophenone, intersystem crossing occurs efficiently between the S-1(n pi(star)) state and the T-1 state of dominant n pi(star) character, leading to excited triplet states after photoexcitation. The transition mechanism between S-1(n pi(star)) and T-1 is still a matter of debate, despite several experimental studies. Quantum mechanical calculations have been performed in order to assess the relative efficiencies of previously proposed mechanisms, in particular, the direct S-1 -> T-1 and indirect S-1 -> T-2(pi pi(star)) -> T-1 ones. Multiconfigurational wave function based methods are used to discuss the nature of the relevant states and also to determine minimum energy paths a…

STATE DIPOLE-MOMENTSPopulationMechanistic organic photochemistryEXCITED BENZOPHENONEGeneral Physics and AstronomyGAS-PHASEABSORPTION-SPECTROSCOPYchemistry.chemical_compoundORGANIC-PHOTOCHEMISTRYMOLECULAR WAVE-FUNCTIONSBenzophenonePhysical and Theoretical ChemistryeducationWave functioneducation.field_of_studyROW ATOMSChemistryCONICAL INTERSECTIONSPhotoexcitation[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryIntersystem crossingExcited state2ND-ORDER PERTURBATION-THEORYANO BASIS-SETSAtomic physicsPhosphorescence
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Coordination polymer flexibility leads to polymorphism and enables a crystalline solid-vapour reaction: a multi-technique mechanistic study.

2015

Despite an absence of conventional porosity, the 1D coordination polymer [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 ] (1; TMP=tetramethylpyrazine) can absorb small alcohols from the vapour phase, which insert into AgO bonds to yield coordination polymers [Ag4 (O2 C(CF2 )2 CF3 )4 (TMP)3 (ROH)2 ] (1-ROH; R=Me, Et, iPr). The reactions are reversible single-crystal-to-single-crystal transformations. Vapour-solid equilibria have been examined by gas-phase IR spectroscopy (K=5.68(9)×10(-5) (MeOH), 9.5(3)×10(-6) (EtOH), 6.14(5)×10(-5) (iPrOH) at 295 K, 1 bar). Thermal analyses (TGA, DSC) have enabled quantitative comparison of two-step reactions 1-ROH→1→2, in which 2 is the 2D coordination polymer [Ag4 (O2 …

In situporosityin situ diffractionCoordination polymerStereochemistrygas-phase spectroscopyInfrared spectroscopyCatalysislaw.inventionpolymorphismchemistry.chemical_compoundOptical microscopelawQDThermal analysisTP155chemistry.chemical_classificationChemistryOrganic ChemistryGeneral ChemistryPolymerCoordination PolymersFull PapersCrystallographyPolymorphism (materials science)microscopysolid-state reactionsPowder diffractionthermal analysisChemistry (Weinheim an der Bergstrasse, Germany)
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A comparison of HONO budgets for two measurement heights at a field station within the boreal forest in Finland

2015

Atmospheric concentrations of nitrous acid (HONO), one of the major precursors of the hydroxyl radical (OH) in the troposphere, significantly exceed the values predicted by the assumption of a photostationary state (PSS) during daytime. Therefore, additional sources of HONO were intensively investigated in the last decades. This study presents budget calculations of HONO based on simultaneous measurements of all relevant species, including HONO and OH at two different measurement heights, i.e. 1 m above the ground and about 2 to 3 m above the canopy (24 m above the ground), conducted in a boreal forest environment. We observed mean HONO concentrations of about 6.5 × 108 molecules cm−3 (26 p…

Meteorologie en Luchtkwaliteit1171 Geosciences4112 ForestryPHOTOLYSIS FREQUENCYMeteorology and Air Qualityeducation116 Chemical sciencesBOUNDARY-LAYERSURFACE-ADSORBED HNO3HETEROGENEOUS HYDROLYSISGAS-PHASE114 Physical scienceslcsh:QC1-999lcsh:ChemistryRING-DOWN SPECTROSCOPYNITRIC-ACIDVERTICAL GRADIENTSlcsh:QD1-999ddc:550Life ScienceNITROUS-ACID HONOATMOSPHERIC CHEMISTRY1172 Environmental scienceslcsh:Physics
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Photochemistry of oxidized Hg(I) and Hg(II) species suggests missing mercury oxidation in the troposphere.

2020

8 pags., 5 figs., 2 tabs.

atmospheric chemistryAtmospheric chemistry010504 meteorology & atmospheric sciencesTropospheric chemistryMercury photoreductionchemistry.chemical_elementatmospheric modelingAtmospheric model010501 environmental sciencesPhotochemistry01 natural sciencesTroposphereMercury oxidationComputer SimulationGas-phase mercury reactivitygas-phase mercury reactivity0105 earth and related environmental sciencesmercury photoreductionThermal oxidationMultidisciplinaryAtmospherePhotodissociationCorrectionMercuryModels TheoreticalPhotochemical Processestropospheric chemistryMercury (element)Atmospheric modelingDeposition (aerosol physics)chemistry13. Climate actionAtmospheric chemistry[CHIM.OTHE]Chemical Sciences/OtherOxidation-ReductionProceedings of the National Academy of Sciences of the United States of America
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Gas-phase ion chemistry of protonated melatonin

2009

The gas-phase ion chemistry of protonated melatonin has been investigated by mass spectrometric (MS) techniques involving chemical ionisation, fast atom bombardment and electrospray ionisation. Either naturally-occurring or collision-induced decomposition experiments have been carried out using side chain tetra-deuterium-labelled derivatives, as well as the corresponding N–D derivatives obtained by exchange with D2O. The analysis of experimental results allows definite pathways for the formation of the ion at m/z 174 to be assigned and sheds some more light on the overall fragmentation pathways. Experiments on labelled derivatives evidenced H–D scrambling processes during fragmentation.

IonsElectrospraySpectrometry Mass Electrospray IonizationChemistryElectrospray ionizationInorganic chemistryDeuterium Exchange MeasurementProtonationmelatonin ESI/MS ESI/MS/MSion chemistryGeneral MedicineFast atom bombardmentPhotochemistryAtomic and Molecular Physics and OpticsIonFragmentation (mass spectrometry)AmmoniaTandem Mass SpectrometryAcetamidesProton affinityQuantum TheoryGasesProtonsSpectroscopyGas-phase ion chemistryMelatonin
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Gas-phase hydrogenation of propionitrile on copper-lanthanide oxides

2009

Abstract The hydrogenation of propionitrile on copper-lanthanide oxide catalysts (2Cu·CeO 2 and 4Cu·Ln 2 O 3 (Ln = La, Pr, Nd)) was studied in the gas phase. The activity of the catalysts varies with the lanthanide in the order 2Cu·CeO 2  > 4Cu·Pr 2 O 3  > 4Cu·La 2 O 3  ≥ 4Cu·Nd 2 O 3 , while the activation energies varies in the opposite order, except for 2Cu·CeO 2 . The main product was the primary amine, n -propylamine. The formation of the unstable imine CH 3 CH 2 N CHCH 3 as a major product over 2Cu·CeO 2 seems to be consistent with the acidity of the catalyst. The catalysts were more selective than conventional copper impregnation catalysts, Cu (10 wt.%) on SiO 2 , La 2 O 3 or CeO 2 ,…

LanthanideCopper oxideInorganic chemistryImineprimary aminechemistry.chemical_element010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysisgas-phase hydrogenationPhysical and Theoretical Chemistrysupported catalystsComputingMilieux_MISCELLANEOUS010405 organic chemistryProcess Chemistry and Technologypropionitrile[CHIM.CATA]Chemical Sciences/CatalysisCopper0104 chemical scienceschemistrycopperAmine gas treatingPropionitrile
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Two Dimensional (2-D) Modeling of a Flat Plate Photocatalytic Reactor for Oxidation of Indoor Air Pollutants

2007

In this paper we present a two-dimensional (2-D) analysis of a narrow-slit, flat-plate, single-pass, flow-through photocatalytic reactor for air purification. The continuity equation for convection and diffusion in two dimensions, under un-steady-state conditions, was coupled with radiation field modeling and photocatalytic reaction kinetics to model the transient and steady-state behavior of the reactor. The model was applied to the photocatalytic oxidation of trichloroethylene (TCE) in humidified air streams under different experimental conditions. The kinetic parameters determined by a three-dimensional (3-D) computational fluid dynamics model of the reactor were used in the 2-D model si…

TRICHLOROETHYLENEHETEROGENEOUS PHOTOCATALYSISGAS-PHASEKINETICS
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A setup to develop novel Chemical Isobaric SEparation (CISE)

2020

Abstract Gas catchers are widely used to thermalize nuclear reaction products and subsequently extract them for precision measurements. However, impurities in the inert stopping gas can chemically react with the ions and thus influence the extraction efficiency. So far, chemical reactions in the gas-catcher have not been investigated in detail. Therefore, we are currently building a new setup to develop Chemical Isobaric SEparation (CISE) with the aim to understand the chemistry inside the gas-catcher and to explore its potential as a new technique for separation of isobars. In this paper, we give a short description of the setup together with the ion transportation studies performed via io…

InertNuclear and High Energy PhysicsGas catcherMass spectrometryNuclear engineeringExtraction (chemistry)Mass spectrometryChemical reactionIonGas-phase chemistryChemical isobaric separationImpuritySTOPPING CELLIsobarIsobaric processInstrumentationIon guideNuclear Instruments & Methods in Physics Research Section B-Beam Interactions with Materials and Atoms
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Entrapment of amino acids in gas phase surfactant assemblies: The case of tryptophan confined in positively charged (1R,2S)-dodecyl (2-hydroxy-1-meth…

2017

The ability of positively charged aggregates of the surfactant (1R,2S)‐dodecyl (2‐hydroxy‐1‐methyl‐2‐phenylethyl))dimethylammonium bromide (DMEB) to incorporate D-tryptophan or L-tryptophan in the gas phase has been investigated by electrospray ion mobility mass spectrometry (ESI‐IM‐MS). Strongly impacted by the pH of the electrosprayed solutions, both protonated (T+) and deprotonated (T-) tryptophan are effectively included into the aggregates, whereas, tryptophan in zwitterionic (T0) form is practically absent in singly charged DMEB aggregates but can be found in multiply charged ones. The ability to incorporate tryptophan increases with the aggregation number and charge state of aggr…

Spectrometry Mass Electrospray IonizationSurfactant aggregateCollision-induced dissociationIon mobilityMolecular ConformationProtonationRandom hexamerGas-phase self-assembly010402 general chemistryPhotochemistry01 natural sciencesGas‐phase self‐assemblychemistry.chemical_compoundSurface-Active AgentsDeprotonationBromideCationsOrganic chemistryMoietyDMEBSpectroscopyAggregation number010401 analytical chemistryTryptophanTryptophanStereoisomerism0104 chemical sciencesQuaternary Ammonium CompoundschemistryGasesJournal of mass spectrometry : JMS
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Probing the low-temperature chemistry of ethanol via the addition of dimethyl ether

2018

Considering the importance of ethanol (EtOH) as an engine fuel and a key component of surrogate fuels, the further understanding of its auto-ignition and oxidation characteristics at engine-relevant conditions (high pressures and low temperatures) is still necessary. However, it remains difficult to measure ignition delay times for ethanol at temperatures below 850 K with currently available facilities including shock tube and rapid compression machine due to its low reactivity. Considering the success of our recent study of toluene oxidation under similar conditions [38], dimethyl ether (DME) has been selected as a radical initiator to explore the low-temperature reactivity of ethanol. In …

IGNITION DELAY020209 energyGeneral Chemical EngineeringRAPID COMPRESSION MACHINEGeneral Physics and AstronomyEnergy Engineering and Power TechnologyLibrary science02 engineering and technologyPRESSURE FLOW REACTORGAS-PHASE7. Clean energychemistry.chemical_compound[SPI]Engineering Sciences [physics]RATE CONSTANTSLow-temperature chemistry020401 chemical engineering0202 electrical engineering electronic engineering information engineeringDMELAMINAR BURNING VELOCITYOrganic chemistryDimethyl ether[INFO]Computer Science [cs]0204 chemical engineeringSHOCK-TUBECHEMICAL-KINETICSComputingMilieux_MISCELLANEOUSEthanolGeneral ChemistryTHERMAL-DECOMPOSITIONIgnition delay timesFuel TechnologychemistryLIQUID FUELS13. Climate action
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