Engineering topics
Publications and source records attributed to Fox, K..
Results of quantum statistical mechanical calculations and thermodynamic evaluation of the structure of H2CO3 and its stability against dissociation are reported. Under temperature and pressure conditions near the surface of Venus, carbonic acid would predominatly dissociate into H2O and CO2 and, hence, could not contribute to any significant absorption there.
Infrared spectra of thin films of pure CH4 have been measured for a range of temperatures from 22 to 68 K. The bandwidth for the fundamental nu3 near 3000/cm varies from 12.7 to 33.2/cm, while that for nu4 near 1300/cm varies from 6.2 to 16.0/cm. The real and imaginary parts of the index of refraction also exhibit significant dependence on temperature. These broadband measurements at low temperatures are useful for an understanding of clouds and hazes in the atmosphere of Uranus, clouds and ices in the atmosphere of Titan, and ices on the surfaces of Pluto and Triton.
A detailed report of the recent high-resolution spectroscopic research on widths and shifts measured for a strong infrared-active fundamental of methane is presented. They were measured in collision with several rare gases and diatomic molecules, in the vibrational-rotational fundamental near 3000/cm. These measurements were made at an ambient temperature of 294 K over a range of pressures from 100 to 700 torr. The measurements are discussed in a preliminary but detailed and quantitative manner with reference to masses, polarizabilities, and quadrupole moments. Some functional dependences on these physical parameters are considered. The present data are useful for studies of corresponding planetary spectra.
A simple revised secular perturbation theory which incorporates the averaged secular effect of first-order near-resonances is derived. By including the effects of these near-resonances, the largest error in the secular frequencies is reduced from 16 percent to less than 3 percent. It is concluded that the revised secular perturbation theory is adequate for the quantitative modeling of the long-term perturbations in the Uranian satellite system. If incorporated within the general theory of Laskar (1986), this theory would lead to completely analytic theory.
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It is demonstrated that the coincidence between Er:YAG laser emission and CH4 absorption is associated with the R(8) multiplet of C-13H4 instead of the R(6) of C-12H4. The Er:YAG emission was characterized as a laser emission at 6079.4/cm with a bandwidh of 2.2/cm and overlapping CH4 emission at 6078.7/cm. The R(6) component of C-12H4 closest to 6078.7/cm is calculated to be 6077.06/cm, corresponding to an absorption coefficient (AC) of 1.12/cm per atm. The F2-prime component of R(8) of C-13H4 has an AC of 0.308/cm per atm, which corresponds well with a range of 1.2-30.30/cm per atm based on a partial pressure of 1.6/89 ppm. The Er:YAG laser is a candidate for use in spectroscopic studies of CH4 atmospheric pollutants, natural gas movement and storage and gas accumulation in coal mines.
Experimental results for the pressure-broadened linewidths gamma of methane are presented and compared with theoretical results. A solar Fourier transform spectrometer with spectral resolving power of about one million was used together with a 6-m base length multitraversal absorption cell. Pressures were determined to an accuracy of + or - 0.2 Torr by means of a capacitance manometer. The pressuring gases were N2, H2, and He. Results are presented for numerical averages of all linewidths corresponding to a given tetrahedral symmetry for J = 0-6. For all cases studied, gamma(E) is found to be substantially less than gamma(A), and gamma(A) is found to be near to, but significantly smaller than, gamma(F). Relative inelastic cross sections calculated for argon scattering from methane are compared with relative pressure-broadened linewidths measured in several experiments involving methane and other gases.
Comprehensive information on the composition and dynamics of the varied planetary atmospheres is summarized. New observations resulted in new demands for supporting laboratory studies. Spectra observed from spacecraft used to interpret planetary atmospheric structure measurements, to aid in greenhouse and cloud physics calculations, and to plan future experiments are discussed. Current findings and new ideas of physicists, chemists, and planetry astronomers relating to the knowledge of the structure of things large and small, of planets and of molecules are summarized.
The planetary atmospheres are investigated for their chemical composition. Hydrogen, methane, ethylene, acetylene, and ethane were studied. Various spectroscopic investigations were made.
The experimental data and theoretical work on the 7.7 micron band of methane are reviewed. This band is particularly relevant in studies of the atmospheres of Jupiter, Saturn and the other outer planets. Methane spectra taken from the infrared spectrometer (IRIS) aboard Voyager, and a temperature profile derived by inverting those data, both for hydrogen and methane are presented.
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The C-12:C-13 ratios in the atmospheres of the outer planets are important parameters with which to test models for isotope formation and fractionation during the early history of the solar system, yielding insight into processes occurring in the primitive solar nebula. The 3 ny sub 3 spectra of methane were obtained using the Kitt Peak Solar Fourier Transform Spectrometer and a 6 m White cell. The experimental results are summarized in a table. The strength ratios for the R-branch of 3 ny sub 3 exhibit strong anomalies, with C-13H4 lines consistently weaker than their C-12H4 counterparts. The C-12:C-13 abundance ratios for the atmospheres of Jupiter and Saturn have been redetermined using the 3 ny sub 3 line-strength ratios measured.
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Anomalous intensity ratios between 2 nu 3 singlet lines of C-13 methane and C-12 methane are reported. Absolute strengths of the Q1, R0 and R1 singlets were measured for essentially pure samples of (C-13)H4 and (C-12)H4 at a resolution of 0.035 kaysers at pressures of 10 and 20 Torr, using a computer controlled grating spectrometer. Line strength ratios between the isotopic species are presented which demonstrate a dramatic effect of isotopic substitution on line strengths. If this effect can be observed in the 3 nu 3 vibration-rotation band of methane, which is widely used in planetary atmosphere studies, revision of the (C-12)H4/(C-13)H4 abundance ratios of the outer planets will be necessary.
The purpose of the Aquifer Thermal Energy Storage Demonstration Program is to stimulate the interest of industry by demonstrating the feasibility of using a geological formation for seasonal thermal energy storage, thereby, reducing crude oil consumption, minimizing thermal pollution, and significantly reducing utility capital investments required to account for peak power requirements. This purpose will be served if several diverse projects can be operated which will demonstrate the technical, economic, environmental, and institutional feasibility of aquifer thermal energy storage systems.
New (C-12)H4 transitions were detected at 21,303 and 94,089 MHz in emission from Orion A, and temporal variations of intensity were observed among several velocity components at 76,700 MHz. An HC5N transition at 21,301 MHz was also detected in emission from IRC +10216.
The identification of gaseous sulfur dioxide on Io by Voyager 1 is reported, and preliminary upper limits for other atmospheric gases are presented. Averaged spectra taken by the Voyager IRIS experiment in the range of 1,000 to 1,200/cm are interpreted as containing three fundamental sulfur dioxide bands, with intensities most nearly corresponding to an atmospheric model with a sulfur dioxide abundance of 0.2 cm atm. Upper limits for COS, CS2, SO3, H2S, CO2, O3, N2O, H2O, CH4, NH3 and HC1, not detected in the spectra, were calculated on the basis of the radiative transfer equation for temperatures of 130 and 250 K; a depletion of hydrogen, carbon and nitrogen is noted. It is suggested that a SO2 outgassing from a cooling sulfur extrusion is the major source of the observed atmospheric SO2.
Absolute intensities have been measured, using a diode laser spectrometer for several vibration-rotation lines in the nu4 fundamental of methane. The data have been analyzed, with the inclusion of Coriolis interactions, to obtain a transition moment of (0.0508 plus or minus 0.0015) x 10 to the minus 18th esu cm. This work appears to resolve some earlier difficulties in interpreting measurements and calculations of intensities in nu4 of CH4.