Rates of hydrogen-graphite reaction between 1550 deg and 2260 deg c
Reaction of graphite and hydrogen in temperature range 1550 to 2260 deg C
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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Kinetics of solid-state reaction of Bi2O3 and Fe2O3
Bismuth oxide and iron oxide equimolar mixtures solid state reactions, determining rates from integrated X ray diffraction and activation energies
Mukherjee, J. L.↗
Study of excitation transfer in a flowing helium afterglow pumped with a tuneable dye laser. 1: Measurement of the rate coefficient for selected quenching reactions involving he(5 3P)
A system is described for the measurement of excited state reaction times in the nanosecond range. A flowing afterglow produces large populations of chemically unstable species, and a pulsed, tuneable dye laser is used to selectively pump these into the reacting excited state. The transient fluorescence from the populations of reactants and end products is used to determine reaction lifetimes and yields. This radiatron is collected with a photon counting system which logs arrival times of spectrally dispersed photons with 10 nanosecond resolution.
Collins, C. B.↗
Kinetics of carbothermal reduction of quartz under vacuum.
Study of the kinetics of carbothermal reduction of quartz in a batch reactor between 0.25 torr and 1 microtorr. The effects of temperature, CO partial pressure, SiO2 phase transformation, and alkali and alkaline-earth oxide additives on the rate of reaction are reported. The results are consistent with a model based on a transitory phase intermediate.
Khalafalla, S. E.↗
Study of excitation transfer in a flowing helium afterglow pumped with a tuneable dye laser. I - Measurement of the rate coefficient for selected quenching reactions involving He/5-3P/.
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Collins, C. B.↗
Rate constant ratio for the reactions of OH with O3 and CO
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Demore, W. B.↗
Role of condensed phase details in the oscillatory combustion of composite propellants
The response functions of composite propellants are theoretically derived, including explicitly the pressure-dependent degradation term in the condensed phase, hypothesizing that the overall rate-limiting reactions are in the relatively low temperature condensed phase. The method of 'inner' and 'outer' expansions with the reduced activation energy as the singular perturbation parameter has been employed. The results cover subsurface reactions with and without surface reactions, adiabatic and uniform-combustion models for the quasi-steady gas phase processes. The response functions display several experimentally observed features like dependence on mean pressure and the instability behavior of some 'zero-n' propellants.
Kumar, R. N.↗
Odd nitrogen in the mesosphere and thermosphere - Its chemistry and transport
The atomic nitrogen in the thermosphere, which is produced either in its ground term or in a highly reactive metastable term, reacts with molecular oxygen to form nitric oxide and atomic oxygen. However, nitric oxide is destroyed in reactions with atomic nitrogen in which molecular nitrogen and atomic oxygen is formed. Adopted reactions and rate coefficients for odd nitrogen chemistry are listed in a table. An analysis is conducted of the temperature distribution below 150 km and its effect on the odd nitrogen chemistry. The latitudinal distribution of nitric oxide is discussed. Satellite measurements have shown that nitric oxide concentrations at high latitudes are highly variable in both time and space. Their average concentrations are 3-4 times higher than at mid-latitudes. The measured variation of nitric oxide density as a function of latitude is shown in a graph.
Rusch, D. W.↗
Modelling of polymer photodegradation for solar cell modules
A computer program developed to model and calculate by numerical integration the varying concentrations of chemical species formed during photooxidation of a polymeric material over time, using as input data a choice set of elementary reactions, corresponding rate constants and a convenient set of starting conditions is evaluated. Attempts were made to validate the proposed mechanism by experimentally monitoring the photooxidation products of small liquid alkane which are useful starting models for ethylene segments of polymers like EVA. The model system proved in appropriate for the intended purposes. Another validation model is recommended.
Somersall, A. C.↗
Modelling of polymer photodegradation for solar cell modules
A computer program which simulates the complex processes of photooxidation which take place in a polymer upon prolonged exposure outdoors causing it to fail in photovoltaic and other applications. The method calculates from an input data set of elementary reactions and rates the concentration profiles of all species over time.
Guillet, J. E.↗
Computations of Emissions Using a 3-D Combustor Program
A general 3-D combustor performance program developed by Garrett was extended to predict soot and NOx emissions. The soot formation and oxidation rates were computed by quasi-global models, taking into account the influence of turbulence. Radiation heat transfer was computed by the six-flux radiation mode. The radiation properties include the influence of CO2 and H2O in addition to soot. NOx emissions were computed from a global four-step hydrocarbon oxidation scheme and a set of rate-controlled reactions involving radicals and nitrogen oxides.
Srivatsa, S. K.↗
Aerothermal modeling
The objectives, approach, and status of a program to develop the computational fluid dynamics tools needed to improve combustor design and analysis are outlined. The calculation procedure selected consists of a finite difference solution of the time averaged, steady state, primitive variable, elliptic form of the Reynolds equations. Standard TEACH type numerics are used to solve the resulting equations. These include hybrid differencing, SIMPLE algorithm for the pressure field, line by line iterative solution using the ADI method and the tridiagonal matrix algorithm (TDMA). Convergence is facilitated by using under relaxation. The physical processes are modeled by a two equation eddy viscosity model for turbulence; combustion is represented by a simple, irreversible, one step chemical reaction whose rate is influenced only by the time scale of the turbulence. The model evaluation procedure is also described.
Sturgess, G. J.↗
Chemoviscosity modeling for thermosetting resins - I
A new analytical model for chemoviscosity variation during cure of thermosetting resins was developed. This model is derived by modifying the widely used WLF (Williams-Landel-Ferry) Theory in polymer rheology. Major assumptions involved are that the rate of reaction is diffusion controlled and is linearly inversely proportional to the viscosity of the medium over the entire cure cycle. The resultant first order nonlinear differential equation is solved numerically, and the model predictions compare favorably with experimental data of EPON 828/Agent U obtained on a Rheometrics System 4 Rheometer. The model describes chemoviscosity up to a range of six orders of magnitude under isothermal curing conditions. The extremely non-linear chemoviscosity profile for a dynamic heating cure cycle is predicted as well. The model is also shown to predict changes of glass transition temperature for the thermosetting resin during cure. The physical significance of this prediction is unclear at the present time, however, and further research is required. From the chemoviscosity simulation point of view, the technique of establishing an analytical model as described here is easily applied to any thermosetting resin. The model thus obtained is used in real-time process controls for fabricating composite materials.
Hou, T. H.↗
On convergence of computation of chemically reacting flows
The computational problems associated with high-temperature flows undergoing finite-rate ionization reactions is investigated. The conservation equations governing chemical species and vibrational and electron energies are solved simultaneously with those for overall mass, momentum, and energy for a one-dimensional subsonic flow, through a constant-area duct, originating behind a normal shock wave, using an implicit time-marching technique. Boundary conditions are imposed in the form of characteristic wave variables accounting for the effects of chemical reactions on the speed of sound. Converging solutions are obtained for cases in which chemical reactions are weak, but difficulty is encountered in other cases. The cause of the difficulty is investigated and shown to be the sharp pressure disturbances produced by such reactions.
Park, C.↗
Memory and subjective workload assessment
Recent research suggested subjective introspection of workload is not based upon specific retrieval of information from long term memory, and only reflects the average workload that is imposed upon the human operator by a particular task. These findings are based upon global ratings of workload for the overall task, suggesting that subjective ratings are limited in ability to retrieve specific details of a task from long term memory. To clarify the limits memory imposes on subjective workload assessment, the difficulty of task segments was varied and the workload of specified segments was retrospectively rated. The ratings were retrospectively collected on the manipulations of three levels of segment difficulty. Subjects were assigned to one of two memory groups. In the Before group, subjects knew before performing a block of trials which segment to rate. In the After group, subjects did not know which segment to rate until after performing the block of trials. The subjective ratings, RTs (reaction times) and MTs (movement times) were compared within group, and between group differences. Performance measures and subjective evaluations of workload reflected the experimental manipulations. Subjects were sensitive to different difficulty levels, and recalled the average workload of task components. Cueing did not appear to help recall, and memory group differences possibly reflected variations in the groups of subjects, or an additional memory task.
Staveland, L.↗
Effect of loading rate on dynamic fracture of reaction bonded silicon nitride
Wedge-loaded, modified tapered double cantilever beam (WL-MTDCB) specimens under impact loading were used to determine the room temperature dynamic fracture response of reaction bonded silicon nitride (RBSN). The crack extension history, with the exception of the terminal phase, was similar to that obtained under static loading. Like its static counterpart, a distinct crack acceleration phase, which was not observed in dynamic fracture of steel and brittle polymers, was noted. Unlike its static counterpart, the crack continued to propagate at nearly its terminal velocity under a low dynamic stress intensity factor during the terminal phase of crack propagation. These and previously obtained results for glass and RBSN show that dynamic crack arrest under a positive dynamic stress intensity factor is unlikely in static and impact loaded structural ceramics.
Liaw, B. M.↗
Measurement of the degree of cure in epoxies with ultrasonic velocity
The use of ultrasonic longitudinal velocity values to measure the degree of cure (defined for an epoxide system as the concentration of epoxide/amine bonds divided by the initial epoxide concentration) in epoxy resins is investigated. The experimental setup used to measure the changes in longitudinal velocity with time is described, together with the technique used to calculate the degree of cure from the acoustic data, using the principle of additive module. Measurements were done with diglycidyl ether of bisphenol A epoxy resin cured with an amine adduct agent. Good qualitative agreement was shown between the time dependence of the acoustically measured degree of cure and the predicted rate of reaction.
Winfree, W. P.↗
A method to eliminate wetting during the homogenization of HgCdTe
Adhesion of HgCdTe samples to fused silica ampoule walls, or 'wetting', during the homogenization process was eliminated by adopting a slower heating rate. The idea is to decrease Cd activity in the sample so as to reduce the rate of reaction between Cd and the silica wall.
Su, Ching-Hua↗