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Publications and source records attributed to Mauersberger, K..
A system with which to calibrate a stratospheric mass spectrometer experiment for ozone has been developed and evaluated. The stability of ozone and the formation of impurities within the calibration volume were measured. The half-life of ozone is about 12 hours, its purity ranges from 95% to 99% and is known to within 1%. The total calibration accuracy of the mass spectrometer experiment for ozone is about + or - 2%.
A mass spectrometer beam experiment and a UV absorption instrument (modified Dasibi instrument) have simultaneously measured ozone mixing ratios in the stratosphere (20-40 km). Both experiments were independently calibrated using absolute standards. The ozone profiles obtained during three balloon descents are in excellent agreement; fine structures are resolved by both experiments. The RMS uncertainty in ozone mixing ratios is about 3% for either instrument.
The structure and composition of the Venus upper atmosphere between 130- and 650-km altitude were measured for a solar zenith angle of approximately 60 deg by the neutral gas mass spectrometer on board the Pioneer Venus multiprobe bus. Below 180 km a wavelike structure is quite evident in the CO2 and He number density profiles. For altitudes above 100 km a one-dimensional model of the Venus upper atmosphere during morningside conditions (MS model) is presented. Number densities at 150-km altitude are as follows: CO2 equals 4.2 x 10 to the 9th, N2 equals 1.1 x 10 to the 9th, CO equals 2.8 x 10 to the 9th, and He equals 4.8 x 10 to the 6th per cu cm. The homopause altitudes for N2 and He are at 136 and 130 km, respectively.
A mass spectrometer experiment for the analysis of minor constituents in the stratosphere has been flown successfully four times from Palestine, Texas on board a balloon gondola. The carbon dioxide mixing ratio, which shows unexpectedly large variations in the stratosphere, reached 400 ppm in one particular night flight. This is about 20% higher than the ground value. Evidence is presented that the experiment performed well during each of the balloon flights. The isotopic ratio C-12/C-13 was measured and found in good agreement with previous air analyses showing a depletion of C-13.
The open source neutral mass spectrometer on board the equatorial Atmosphere Explorer E satellite (AE-E) measured atomic nitrogen densities at frequent intervals during both the elliptical and circular orbit phases of satellite operations. Elliptical orbit data presented here by means of empirical models at 225- and 300-km altitude provide diurnal and seasonal profiles at altitudes lower than previously possible. Data from individual circular orbits later in the AE-E mission confirm essential features of these models, particularly the diurnal density profile. At lower altitudes, considerable variation is evident near midnight, with density enhancements correlated with increasing levels of geomagnetic activity.
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A gas expansion system combined with a mass spectrometer has been tested and flown successfully in the stratosphere. Through a sequence of orifices and high speed pumping, gas particles were formed into a molecular beam and analyzed by a sensitive mass spectrometer. During two balloon flights, vertical profiles of all major atmospheric constituents as well as O3, CO2, H2O and others were obtained. Gases such as AR38 and O16;O17 provided in-flight calibration standards. The sensitivity of the system was such that gases with mixing ratios of 10 ppb at an ambient pressure of about 10 mbar were detectable.
On December 9, 1978 the neutral gas mass spectrometer aboard the NASA Pioneer Venus multiprobe bus has measured density, composition, and temperature of the Venus dayside thermosphere. There was no positive identification of argon down to the lowest measuring altitude of 130 km. For the altitude level of 135 km the following upper limits for the number densities of argon isotopes were derived: n(Ar-36) less than 1.3 times 10 to the 6th power per cu cm and n(Ar-40) less than 2.8 times 10 to the 6th power per cu cm. From our upper atmosphere observations we infer for the troposphere of Venus the following upper limits for the mixing ratios: n(Ar-36)/total number density less than 9 times 10 to the minus 6th power and n(Ar-40)/total number density less than 20 times 10 to the minus 6th power.
The paper presents a simplified model of the ion source chemistry, explains several details of the data reduction method used in obtaining atomic-nitrogen (N) densities from OSS data, and discusses implications of gas-surface reactions for the design of future satellite-borne mass spectrometers. Because of various surface reactions, N appears in three different forms in the ion source, as N, NO, and NO2. Considering the rather small spin modulation of NO and NO2 in the semi-open ionization chamber used in the OSS instrument, it is not surprising that these reaction products have not been previously identified in closed source instruments as a measure of the presence of atomic nitrogen. Warmup and/or outgassing of the ion source are shown to drastically reduce the NO2 concentration, thereby making possible reliable measurement of ambient N densities.
The neutral mass spectrometer on board the Pioneer Venus multiprobe bus measured composition and structural parameters of the dayside Venus upper atmosphere on 9 December 1978. Carbon dioxide and helium number densities were 6 x 10 to the 9th and 5 x 10 to the 6th per cubic centimeter, respectively, at an altitude of 150 kilometers. The mixing ratios of the both argon-36 and argon-40 were approximately 80 parts per million at an altitude of 135 kilometers. The exospheric temperature from 160 to 170 kilometers was 285 plus or minus 10 K. The helium homopause was found at an altitude of about 137 kilometers.
For the in situ investigation of planetary atmospheres a small Mattauch-Herzog mass spectrometer has been developed. Its high-pressure performance has been improved by incorporating differential pumping between the ion source and the analyzing fields, shortening the path-length as well as increasing the extraction field in the ion source. In addition doubly ionized and dissociated ions are used for mass analysis. These measures make possible operation up to 0.01 millibars. Results of laboratory tests related to linearity, dynamic range, and mass resolution are presented, in particular for CO2.
Theoretical calculations of the seasonal and diurnal variations of atomic nitrogen are compared with measurements made by the open source neutral mass spectrometer on the AE-C satellite. With the simultaneous measurements of molecular nitrogen and atomic oxygen densities as input, model calculations of odd nitrogen densities predict the same trends in atomic nitrogen as those observed. From these comparisons it is inferred that horizontal transport significantly reduces the diurnal variation of atomic nitrogen. Estimates are given of the sensitivity of atomic nitrogen densities to variations in the photoelectron flux, the neutral temperatures, and the neutral winds.
An experimental concept for investigation of planetary atmospheres using a mass spectrometer is discussed. High atmospheric pressures are reduced to mass spectrometer operating pressures by means of differential pumping. Sampling is accomplished through the formation of a molecular beam. A flag in front of the mass spectrometer can be used to separate ambient gases from system background. Laboratory tests have confirmed the feasibility of the experiment, particularly in CO2 dominated atmospheres.
A special gas inlet system is required for reduction of high ambient pressures to ion source operating pressures for mass spectrometer investigations in the stratosphere for the determination of the abundance of minor constituents. A system has been designed which combines a mass spectrometer and a gas inlet system reducing pressure by differential pumping using high-speed liquid helium pumps and small orifices. The gas particles are formed into a neutral beam with a flag mechanism proceeding into the mass spectrometer ion source where they are ionized for subsequent mass separation. A laboratory model has been tested under conditions simulating stratospheric pressures. It was shown that the process is able to identify gases with abundances below 10 to the -8th. Some of the problems associated with gas analysis of trace constituents have been alleviated, and other applications of the system have been identified, such as pollution control and medicine.
Special operating modes of the open source neutral mass spectrometer (OSS) on the Atmosphere Explorer C permit the measurement of odd nitrogen (N + NO) number densities between 180 and 450 km. By using optical measurements of NO concentrations from the ultraviolet nitric oxide experiment on AE-C, number densities of N are obtained. Altitude profiles for the midlatitude legs of three orbits in the late spring of 1974 are presented and compared with densities predicted by the AE-C (OSS) empirical N model at 375 km. Atomic nitrogen appeared to be in diffusive equilibrium at least above 200 km in each of the orbits studied. A typical number density of N at 200 km, 0900 LST, and 40 deg N latitude in late May 1974 is 30 million per cu cm.
Atomic nitrogen number densities in the upper thermosphere measured by the open source neutral mass spectrometer (OSS) on Atmosphere Explorer-C during 1974 and part of 1975 have been used to construct a global empirical model at an altitude of 375 km based on a spherical harmonic expansion. The most evident features of the model are large diurnal and seasonal variations of atomic nitrogen and only a moderate and latitude-dependent density increase during periods of geomagnetic activity. Maximum and minimum N number densities at 375 km for periods of low solar activity are 3.6 x 10 to the 6th/cu cm at 1500 LST (local solar time) and low latitude in the summer hemisphere and 1.5 x 10 to the 5th/cu cm at 0200 LST at mid-latitudes in the winter hemisphere.
The open source neutral mass spectrometer on board the Atmosphere Explorer satellites measures, besides other neutral constituents, atomic nitrogen densities in the upper thermosphere. Atomic nitrogen combines with atomic oxygen on the walls of the mass spectrometer ion source to form NO. From the measured NO concentration atomic nitrogen is deduced. Studies of the diurnal variation show that the maximum atomic nitrogen densities occur near 1600 local solar time (LST) and minimum densities near 0400 LST. The diurnal amplitude at 300 km is about a factor of 8, which is lower than predicted in present models. Atomic nitrogen also exhibits a pronounced seasonal variation with an amplitude similar to that of the diurnal variation; summer values are considerably higher than winter ones.
The elliptical and circular phases of the Atmosphere Explorer-C satellite have provided the basis for a study of the neutral wave characteristics in the thermosphere using data collected by the open source mass spectrometer used to measure both reactive (O,N) and nonreactive (O2, N2, He, Ar) constituents. The phase relationships between the constituents are discussed and the results of a wave occurrence and amplitude survey covering 338 despun orbits in which the local time and latitude characteristics of the waves are presented are discussed. Conclusions based on this survey are tested in a study of waves measured at high latitudes during a geomagnetic storm.