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At least 217 records · Page 12

Model calculations of the dayside ionosphere of Venus - Ionic composition

Comprehensive model calculations of the dayside ion density distributions were carried out and compared with results from the Pioneer Venus ion mass spectrometer. The coupled continuity and momentum equations were solved for O2(+), O(+), CO2(+), C(+), N(+), He(+), and H(+) densities for altitudes well away from the ionopause, where the horizontal transport terms are negligible. Chemical equilibrium solutions, describing conditions below about 200 km, were also obtained for N2(+), NO(+), and CO(+). The agreement between the model calculations of ion density and the measurements is good for some species, such as O(+), and rather poor for others, such as CO(+), indicating that while a basic understanding of the major chemical and physical processes controlling the composition and vertical distribution of the dayside Venus ionosphere, well below the ionopause, has been achieved, there are many important details requiring further investigations.

Nagy, A. F.↗

About the parametric interplay between ionic Mach number, body-size, and satellite potential in determining the ion depletion in the wake of the S3-2 satellite

The variation of ion current depletion in the wake of the U.S. Air Force satellite S3-2 is quantitatively determined, taking into account altitudes in the range from 300 to 1100 km. The considered investigation has the objective to present results which besides of being of scientific interest per se are useful to the planning of future experiments of body-plasma electrodynamic interactions in a supersonic and sub-Alfvenic flow regime to be conducted on board the Shuttle/Spacelab. More specifically, it is expected that the outcome of investigations of the kind presented will be useful in the planning of instrument location on ejectable ensembles of probes and on the Orbiter itself in future Shuttle/Spacelab missions.

Samir, U.↗

Ionic Refrigerator

With no moving parts, proposed refrigerator has long life. Thermal energy of refrigeration process transported by hydrogen ions that go through three phase changes in absorbing heat and three phase changes in dissipating heat.

Richter, R.↗

Termolecular ionic recombination at high ambient gas density

It is shown that the importance of diffusion relative to drift in ion-ion recombination is a decreasing function of the separation between the ions (contrary to a common supposition). Langevin's formula for the recombination coefficient is obtained very simply using a physical model which allows for both diffusion and drift.

Bates, D. R.↗

Direct determination of the ionic charge distribution of heavy ions in Fe-rich solar energetic particle events

The first direct determination of the iron charge distribution in the energy range 0.3-1.0 MeV/nucleon during Fe-rich and He-3-rich solar energetic particle events is reported. The deterimination was made on the basis of ISEE-3 data for the event from August 1978 to October 1979. The enrichment of He-3 iron relative to oxygen was found to be directly correlated with the enrichment of He-3 to He-4. Average ion charge distributions were computed for: (1) He-3-rich periods which were also Fe-rich and had a He-3/He-4 ratio of 0.1 and (2) periods with a He-3/He-4 ratio of less than 0.1. It is found that the mean iron charge state for He-3-rich periods was in the range 19.5 (+ or - 1.5) and only 14 (+ or - 1) for the time periods with He-3/He-4 less than ratio of 0.1. The reduced data are found to be in good agreement with the theoretical predictions of Fisk (1978), suggesting a temperature in the source region above 5 million degrees K for Fe-rich and He-3-rich solar energetic particle events.

Klecker, B.↗

Ionic charge distributions of energetic particles from solar flares

The effects which solar flare X-rays have on the charge states of solar cosmic rays is determined quantitatively. Rather than to characterize the charge distribution by temperature alone, it is proposed that the X-ray flux at the acceleration site also is used. The effects of flare X-rays are modeled mathematically.

Mullan, D. J.↗

Theoretical dissociation energies for ionic molecules

Ab initio calculations at the self-consistent-field and singles plus doubles configuration-interaction level are used to determine accurate spectroscopic parameters for most of the alkali and alkaline-earth fluorides, chlorides, oxides, sulfides, hydroxides, and isocyanides. Numerical Hartree-Fock (NHF) calculations are performed on selected systems to ensure that the extended Slater basis sets employed for the diatomic systems are near the Hartree-Fock limit. Extended Gaussian basis sets of at least triple-zeta plus double polarization equality are employed for the triatomic system. With this model, correlation effects are relatively small, but invariably increase the theoretical dissociation energies. The importance of correlating the electrons on both the anion and the metal is discussed. The theoretical dissociation energies are critically compared with the literature to rule out disparate experimental values. Theoretical (sup 2)Pi - (sup 2)Sigma (sup +) energy separations are presented for the alkali oxides and sulfides.

Langhoff, S. R.↗

Nuclear and ionic charge distribution experiment on ISEE-1 and ISEE-3

The experimental work carried out under this contract is a continuation of that originally performed under Contracts NAS5-20062 and NAS5-26739. The data analyzed are from the Max-Planck Institut/Univ. of Maryland experiment on ISEE-1 and ISEE-3. Each spacecraft experiment consists of a nearly identical set of three sensors (designated the ULECA, ULEWAT, and ULEZEQ sensors) designed to measure the energy spectra and composition of suprathermal and energetic ions over a broad energy range (less than 3 keV/e to more than 20 MeV/nucleon). Since the launch of ISEE's 2 and 3, the MPI/Univ. of Maryland experiments have generally performed as expected except for a partial failure of the ULEWAT sensor on ISEE-1 in August 1978. A number of scientific studies have either been completed, initiated or are at various stages of completion. A brief summary of Primary Results is given, followed by a more detailed summary of the major accomplishments at the Univ. of Maryland.

Gloeckler, G.↗

Ionic rotational branching ratios in resonant enhanced multiphoton ionization of NO via the A2Sigma(+)(3s sigma) and D2Sigma(+)(3p sigma) states

Results are presented for the rotationally resolved photoelectron spectra resulting from a (2 + 1) one-color resonant enhanced multiphoton ionization (REMPI) of NO via the rotationally clean S21(11.5) and mixed S11(15.5) + R21(15.5) branches of the 0-0 transition in the D-X band. The calculations were done in the fixed-nuclei frozen core approximation. The resulting photoionization spectra, convoluted with a Lorentzian detection function, agree qualitatively with experimental results of Viswanathan et al. (1986) and support their conclusion that the nonspherical nature of the molecular potential creates a substantial l-mixing in the continuum, which in turn leads to the intense Delta N = 0 peak. The rather strong photoelectron energy dependence of the rotational branching ratios of the D 2Sigma(+) S21(11.5) line was investigated and compared to the weak energy dependence of the A 2Sigma(+) R22(21.5) line.

Rudolph, H.↗

(1 + 1) resonant enhanced multiphoton ionization via the A2Sigma(+) state of NO - Ionic rotational branching ratios and their intensity dependence

Rotational branching ratios resulting from the (1 + 1) resonant enhanced multiphoton ionization spectroscopy of NO via the 0-0 transition of the A-X band for the four possible branches that can be assigned as R(21.5) are explored using calculation performed in the frozen-core approximation at the Hartree-Fock level. The four different branches, of which three are distinctly different in the perturbative limit, have rather different branching ratios. The mixed R12 + Q22(21.5) branch, which is not intense and has the lowest transition energy, appears to give the best agreement with experimental branching ratio for parallel detection. The agreement is less satisfactory for perpendicular detection. Neither the effect of finite-acceptance angle of the photoelectron detector nor high intensities can explain the discrepancy.

Rudolph, H.↗

Ionic mechanisms subserving mechanosensory transduction and neural integration in statocyst hair cells of Hermissenda

The neural processing of gravitational-produced sensory stimulation of statocyst hair cells in the nudibranch mollusk Hermissenda was studied. The goal in these studies was to understand how: gravireceptor neurons sense or transduce gravitational forces, gravitational stimulation is integrated so as to produce a graded receptor potential, and ultimately the generation of an action potential, and various neural adaptation phenomena which hair cells exhibit arise. The approach to these problems was primarily electrophysical.

Farley, Joseph↗

Ionic binding properties of carrier ampholytes

Radioactive ampholytes were synthesized with specific activity of 638 microCi/g. These were used in studies of ampholyte binding to target proteins under nonionic conditions. These radioactive ampholytes bound to target proteins but were dissociable in sodium chloride solutions with dissociation occurring in a concentration dependent way. The ampholytes could be dissociated from target molecules using excess unlabelled ampholytes synthesized in the laboratory as well as commercial ampholytes. Radioactive ampholytes were bound to target proteins with different isoelectric points, and the bound ampholytes were eluted and analyzed by recycling isoelectric focusing. The results showed that acidic proteins bound basic ampholytes and basic proteins bound acidic ampholytes.

Rodkey, L. Scott↗

Nonvolatile Ionic Two-Terminal Memory Device

Conceptual solid-state memory device nonvolatile and erasable and has only two terminals. Proposed device based on two effects: thermal phase transition and reversible intercalation of ions. Transfer of sodium ions between source of ions and electrical switching element increases or decreases electrical conductance of element, turning switch "on" or "off". Used in digital computers and neural-network computers. In neural networks, many small, densely packed switches function as erasable, nonvolatile synaptic elements.

Williams, Roger M.↗

An ionic mechanism of carbon formation in flames

The formation of incipient carbon in flames can be described by a series of elementary reactions in which the precursor of soot is the ion C3H3+, and the major building block is acetylene, polyacetylenes, or other hydrocarbon fragments which are present in large concentrations. The precursor ion is produced by nonequilibrium chemi-ionization reactions, e.g., CH asterisk plus C2H2 yields C3H3+ plus e or CH asterisk plus O yields CHO+ plus e. The CHO+ rapidly becomes C3H3+ through a series of ion-molecule reactions. The chemi-ion then adds acetylene in a series of very rapid ion-molecule reactions producing larger and larger ions. Ions isomerize very rapidly to produce aromatic structures overcoming one of the major problems with neutral species mechanisms: how to form the first carbon ring. As the ions grow, their recombination rate coefficients with electrons increase so that the larger ions are removed by dissociative recombination. These neutral species now continue to grow by the addition of more acetylene producing even larger neutral species. With increasing size, the rate coefficient of electron attachment also increases causing the reaction to become important, depending upon the temperature. Appreciable concentrations of negative ions shift the ion removal process to dissociative ion-ion recombination, which is orders of magnitude slower than ion-electron recombination. As the neutral species continue to grow by the addition of acetylene, they gradually take on the aspect of particles, i.e., the bulk properties of the substance CxHy dominate over the chemical properties. This change is gradual and there is no distinct size at which a large molecule becomes a particle. Evidence will be presented supporting the above mechanism. All of the ions proposed in the mechanism have been observed by mass spectrometric analysis, their concentrations measured, and their rates of reaction in the flame environment determined to be adequate to account for the observed rate of formation of carbon.

Calcote, H. F.↗

12-crown-4 ether-assisted enhancement of ionic conductivity and interfacial kinetics in polyethylene oxide electrolytes

The electrical and electrochemical properties of thin films of polyethylene oxide electrolytes with and without 12-crown-4 ether (12Cr4) are studied as a function of temperature and in the frequency regime from 100 kHz to 0.1 Hz. These measurements were made on electrolytes containing LiCF3SO3, LiBF4, or LiClO4 salts. At a given temperature, the bulk conductivity for a particular salt depends on the 12Cr4 concentration, reaching a maximum for a ratio of 12Cr4 to Li of 0.003.

Nagasubramanian, G.↗

Effects of 12-Crown-4 ether on the ionic conductivity and electrode kinetics of electrolytes in polyethylene oxide

Results are described of investigations of the electrical and electrochemical properties of thin films of polyethylene oxide (PEO) electrolytes with and without 12-Crown-4 ether (12Cr4) as a function of temperature and in the frequency regime 100 kHz-0.1 Hz. These measurements were made for LiCF3SO3, LiBF4, and LiClO4 salts. At a given temperature, the bulk conductivity, sigma, (S/cm), for a particular salt, depends on the 12Cr4 concentration with sigma reaching a maximum at about 3 mM 12Cr4. Of the three salts studied, the sigma is the highest for PEO/LiBF4 with 3 mM 12Cr4. The ac and dc measurements yield a lower charge transfer resistance for 12Cr4-incorporated samples than for samples without. Plating/stripping of Li occurs at a potential closer to Li(+)/Li for 12Cr4 samples than those without. The conductivities of a thin (about 100 microns) and a thick (400 microns) films are similar.

Nagasubramanian, G.↗