The Journal of Chemical Physics · 1973 · 27 citations · 5 references
EngineeringMeasurementRate CoefficientExperimental ThermodynamicsChemistryIon ProcessSpectrochemical AnalysisChemical EngineeringAnalytical InstrumentationMolecular ThermodynamicsTransport PhenomenaThermodynamicsInstrumentationMolecular KineticsReaction ProcessBiophysicsChemical ThermodynamicsPhysicsReactions H+Physical ChemistryHydrogenEnergyUniform Electric FieldProton TransferMass SpectrometryIon DriftingMedicineChemical Kinetics
The rate coefficient of the reaction H+ + 2H2 → H3+ + H2 has been measured at a gas temperature of 300 °K and over a pressure range 0.25–0.50 torr. The transport properties and average energy of a given species of ion drifting in a gas in a uniform electric field are determined by E/N, where E is the electric field intensity and N is the gas number density. E/N is expressed in units of the townsend (Td), where 1 Td = 10−17 V · cm2. Our measurements were made over a range 25–50 Td, where the lower value corresponds to an average energy for the reacting H+ ions which is very close to the thermal energy of the H2 molecules at 300 °K. No systematic variation of the rate coefficient was observed over the range of E/N which was covered. The measurements were made with a drift tube mass spectrometer and involved the detailed analysis of the arrival time spectra of the product H3+ ion. The rate coefficient was evaluated to be (3.05 ± 0.15) × 10−29 cm6/sec. The same result was also obtained for the reaction D+ + 2D2 → D3+ + D2.
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Motion of Gaseous Ions in Strong Electric Fields
Gregory H. Wannier · Bell System Technical Journal · 1953 · 615 citations
R. M. Snuggs, D. J. Volz, J. H. Schummers et al. · Physical review. A, General physics · 1971 · 98 citations
Longitudinal Diffusion Coefficient, Engineering, Nuclear Physics +22