Engineering topics
Publications and source records attributed to Aikin, A. C..
For comets whose nuclei are composed of water ice conglomerates it is shown that the ion H3O(+) can predominate to distances of 5000 km in the subsolar direction. Beyond this distance H2O(+) is the most important ion. The crossover point is a sensitive function of the rate of evaporation from the nucleus. The presence of ammonia or metals such as sodium, in concentrations greater than 0.1% H2O, can lead to NH4(+) and Na(+) ions.
The first in situ measurements of ion composition in the nighttime equatorial E- and F-region ionospheres are presented and discussed. These profiles were obtained by two rocket-borne ion mass spectrometers launched from Thumba, India, on March 9-10, 1970. Ionosonde data established that the composition was measured at times bounding a period of F-region downward drift. During this period, the ions O(+) and N(+) were enhanced by 1-3 orders of magnitude between 220 and 300 km. Below the drift region, O(+) ceased to be the major ionic constituent, but the concentrations of O(+) and N(+) remained larger than predicted from known radiation sources and loss processes. Here also, both the O2(+) and the NO(+) profiles retained nearly the same shape and magnitude throughout the night in agreement with theories assuming scattered UV radiation to be the maintaining source.
For comets whose nuclei are composed of water ice conglomerates it is shown that the ion H3O(+) can predominate to distances of 5000 km in the subsolar direction. Beyond this distance H2O(+) is the most important ion. The crossover point is a sensitive function of the rate of evaporation from the nucleus. The presence of ammonia or metals such as sodium, in concentrations greater than 0.1% H2O, can lead to NH4(+) and Na(+) ions.
The first in situ measurements of ion composition in the nighttime equatorial E and F region ionospheres (90-300 km) are presented and discussed. These profiles were obtained by two rocket-borne ion mass spectrometers launched from Thumba, India on March 9-10, 1970 at solar zenith angles of 112 deg and 165 deg. Ionosonde data established that the composition was measured at times bounding a period of F region downward drift. During this period the ions O(+) and N(+) were enhanced by one to three orders of magnitude between 220 and 300 km. Below the drift region (200 km), O(+) ceased to be the major ionic constituent, but the concentrations of O(+) and N(+) remained larger than predicted from known radiation sources and loss processes. Here also, both the O2(+) and NO(+) profiles retained nearly the same shape and magnitude throughout the night in agreement with theories assuming scattered UV radiation to be the maintaining source. Light metallic ions including Mg(+), Na(+) and possibly Si(+) were observed to altitude approaching 300 km, while the heavier ions Ca(+) and K(+) were seen in reduced quantity to 200 km. All metal ion profiles exhibited changes which can be ascribed to vertical drifting.
The positive ion composition within a mid-latitude sporadic E layer has been measured with the aid of a rocketborne ion mass spectrometer launched from El Arenosillo, Spain on July 3, 1972 at 0743 LMT. Ionograms taken before and during the rocket flight showed a developing sporadic E layer near 114 km. Rocket data showed peaks in electron density and metallic ions at this same height. Both the maximum and total content of the metals are observed to be greater on the downleg than on the upleg measurement.
Two ion composition profiles, representative of the nighttime equatorial ionosphere between 90 km and 300 km, are presented. These profiles were obtained by two rocket-borne ion mass spectrometers on a single night for solar zenith angles of 112 deg and 165 deg. For both flights, the principal ion above 200 km is O(+). The downward drift of the atomic ions O(+) and N(+), coinciding with the postsunset lowering of the F2 peak, is observed through an enhancement of the density of O(+) at altitudes above 200 km and N(+) above 240 km. Below the drift region, O(+) and N(+) are observed in concentrations larger than expected. The NO(+) altitude distribution retains its shape throughout the night, and below 210 km, is the principal ion. The behavior of O2(+) can be explained by the O(+), electron density and theoretical neutral nitric oxide concentrations. Light metallic ions, including Mg(+), Na(+), and possibly Si(+), are observed to altitudes approaching 300 km and are affected by vertical drift.
The positive ion composition within a midlatitude sporadic E layer has been measured with the aid of a rocket-borne ion mass spectrometer launched from El Arenosillo, Spain on July 3, 1972 at 0743 LMT. Ionograms taken before and during the rocket flight showed a developing sporadic E layer near 114 km. Rocket data showed peaks in electron density and metallic ions at this same height. Both the maximum and total content of the metals are observed to be greater on the downleg than the upleg measurement.
Metal ion density measurement in sporadic E layer during beta Taurids shower by rocket-borne mass spectrometry, noting origin in cosmic debris ablation
A numerical model of eddy diffusive transport of emitted gases from the space shuttle wake, including chemical reactions between the emitted constituents and the ambient atmosphere, has been constructed for 75 km altitude. The numerical methods involve explicit solution of the diffusion equation and Runge-Kutta method for the chemical reactions. The time required to reach background levels of nitric oxide concentration of 7 x 10 to the 7th power molecules/cc has been calculated. This relaxation time depends strongly on atmospheric conditions.
The positive nitrogen peroxide ion is discussed as an ionic constituent of the lower ionosphere in the light of recently observed concentrations at altitudes between 87.8 and 93.2 km. Photoionization and charge exchange reactions appear to be insufficient to account for the positive nitrogen peroxide ion concentration observed at 90 km. A possible alternative reaction is proposed, and its implications are briefly reviewed.
Four positive ion composition measurements of the equatorial E region at Thumba, India, are presented. During the day, the major ions between 90 and 125 km are NO+ and O2+. The relative concentrations are similar to those observed at midlatitudes but exhibit unusual structural behavior with altitude. A metallic ion layer centered at 92 km is found to contain Mg+, Fe+, Ca+, K+, Al+, Na+, and possibly Si+ ions. The layer is explained in terms of a similarly shaped altitude distribution of neutral atoms that are photoionized and charge exchanged with NO+ and O2+. Three-body reactions form molecular metallic ions that are rapidly lost by dissociative ion-electron recombination.
Positive metallic ions have been measured in the earth's atmosphere between 85 and 120 km, during the period of the beta Taurids meteor shower, which is associated with Comet Encke. The ions originate during and following ablation of extraterrestrial debris by the earth's atmosphere. The enhancement of metal ion density during meteor showers is primary evidence for their extraterrestrial origin. The present results were obtained from a rocket-borne ion mass spectrometer.
To monitor the descriptive parameters of the lower ionosphere and construct a model which predicts their temporal and spatial variations is a particularly difficult task. In a given situation simultaneous measurements should be conducted of ionization sources, the altitude distribution of all neutral atmospheric constituents, the identification, number density, and altitude distribution of different species of positive and negative ions and electrons. These results are compared with theoretical predictions to serve as boundary conditions and guides to modification of the theory. It has not been possible to realize this goal in lower ionosphere research because of the large number of parameters and since certain parameters, such as positive ion species distribution and nitric oxide, can only be measured with the aid of sounding rockets. To illustrate the difficulty, recent positive ion composition measurements are compared with predictions utilizing clustering of ions and neutrals to form hydrated ions.
Metal ions including Na-40(+), Mg-24(+), Si-28(+), K-39(+), Ca-40(+), Sc-45(+), Cr-52(+), Fe-56(+), and Ni-58(+) were detected in the upper atmosphere during the beta Taurids meteor shower. Abundances of these ions relative to Si(+) show agreement in most instances with chondrites. A notable exception is 45(+), which is Sc(+), is 100 times more abundant than neutral scandium found in chondrites.
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Data on the NO2(+)(46 AMU) were obtained with a rocket-borne quadrupole ion mass spectrometer. The ion 46(+) is most prevalent in the vicinity of 90 km and is always observed in the presence of 48(+), identified as NO(+)-H2O. The observed concentrations of O(+)(16), O2(+)(32), NO2(+)(46), NO(+)-H2O(48), electrons, and the ratio 48(+)/46(+) are tabulated for altitudes from 87.8 to 93.2 km. Reactions governing the distribution of NO2(+) are briefly discussed, and it is felt that photoionization and charge exchange reactions are insufficient to account for the NO2(+) concentration at 90 km.
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The daytime ionosphere of Venus is observed between 100 and 500 km altitude. Below 200 km, CO2(+) is thought to be the principal ion unless oxygen is present. It was suggested that at altitudes less than 130 km the ion CO2(+)-CO2 is an important ionic constituent of the Venus ionosphere. Below 100 km, ion clustering processes combine with the low temperature at the mesopause to form coagulates giving rise to the ultraviolet haze layer which is frequently observed.