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The isolation of three hydantoins from HCN oligomers is described. One of these hydantoins, 5-carboxymethylidine hydantoin (5-CMH), rearranges to pyrimidine orotic acid in basic solution. The isolation of 5-CMH suggests the possibility that pyrimidines were formed directly from HCN on the primitive earth.
Observations are reported of the 2.6-mm line of CO from an extended region in Monoceros containing a complex of dust clouds as well as a group of reflection nebulae (Mon R2) and where a source of relatively strong millimeter emission from CS and HCN has been found. Lower limits are obtained for the CO and H2 column densities in this region, and five CO emission peaks are identified, each of which is approximately coincident with at least one reflection nebula. Around the position of the strongest peak, extended emission is observed from CS and HCN, suggesting the existence of a rotating core with an H2 density which corresponds to a mass of 5500 solar masses. The CO profiles in the direction of the strongest peak appear to show self-absorption, which may indicate a collapsing cloud.
The origin of the high-speed HCN jets observed in Comet Kohoutek (1973f) is considered. It is argued that the occurrence of these jets with Doppler shifts corresponding to velocities of approximately 3-5 km/s with respect to the nucleus cannot be explained in terms of either explosive outbursts of trapped sub-surface volatiles, highly exothermic chemical reactions involving free radicals, or the outward expansion of the cometary atmosphere with additional heating. Instead, acceleration of the precursor ions of HCN by energetic electrons in the ionospheric current sheets or current arcs is suggested to play an important role.
Limits on column densities and production rates are derived in light of negative results from a search for HCN, CS, and CH3OH millimeter-wave emissions, along with two unidentified lines observed in Comet Kohoutek (1973 XII), from Comet Bradfield (1979l) after perihelion passage. In the case of HCN, the production rate is found to be lower than that reported for Comet Kohoutek even upon scaling of measurements relative to the observed OH emission from each comet.
Far infrared limb thermal emission measurements of the earth's stratosphere were made with a high resolution spectrometer on a balloon payload launched from Palestine, TX, on Oct. 5, 1982. Several limb sequences of a portion of the observed spectra have been analyzed for retrieval of the stratospheric HCN profile from a number of spectral lines in the 32 to 56 cm region. The mixing ratio profile in the 20 to 37 km altitude range has been retrieved with 2-sigma uncertainties of about 4-5 km. The HCN volume mixing ratio is found to be about 139 pptv at 20 km, 127 pptv at 25 km, and increasing to 172 pptv at 37 km. The results are compared with measurements by other groups and with photochemical model calculations reported in the literature.
Middle and upper stratospheric HCN has been measured using ground-based mm-wave emission spectroscopy during a series of observations made in Mauna Kea, HI, in June 1986. A volume mixing ratio of 190 + or - 40 pptv at about 40 km, and a decrease of concentration with altitude that is considerably slower than that predicted by current models are found. This could be an indication of an atmospheric source of HCN as yet unidentified.
The concentrations in the mesosphere of H2O, CH4, H2CO, H2O2, and HCN were inferred from data on positive ion compositions, obtained from one mid-latitude and four high-latitude rocket flights. The inferred concentrations were found to agree only partially with the ground-based microwave measurements and/or model prediction by Garcia and Solomon (1985). The CH4 concentration was found to vary between 70 and 4 ppb in daytime and 900 and 100 ppbv at night, respectively. Unexpectedly high H2CO concentrations were obtained, with H2CO/H2O ratios between 0.0006 and 0.1, and a mean HCN volume mixing ratio of 6 x 10 to the -10th was inferred.
Saturn, Uranus, and Neptune were observed at millimeter wavelengths with the IRAM 30 m telescope. The major result is the detection of CO and HCN in Neptune's stratosphere, with respective mixing ratios of (6.5 +/- 3.5) x 10 exp -7 and (3 +/- 1.5) x 10 exp -10. CO seems to be present in Neptune's troposphere as well and to slowly decrease with altitude (scale height about 200 km). HCN is probably formed from reactions between CH3 and N, which can be supplied in sufficient amounts by escape from Triton's atmosphere. The origin of CO, however, is more problematic, because: (1) thermochemical models fail to reproduce the observed abundance by a factor of about 1000; and (2) an external source would require a very large flux of oxygen. CO appears to be at least 15 times less abundant on Uranus than on Neptune. Finally, an upper limit of 10 exp -7 for CO in Saturn's stratosphere suggests an internal origin for Saturnian CO.
Volume mixing ratio (VMR) profiles of OCS, HCN, SF6, and CHClF2 (HCFC-22) have been measured near 30 deg N latitude by the Atmospheric Trace Molecule Spectroscopy Fourier transform spectrometer during shuttle flights on 29 April - 6 May 1985 and 3-2 November 1994. The change in the concentration of each molecule in the lower stratosphere has been derived for this 9 1/2-year period by comparing measurements between potential temperatures of 395 to 800 K (approximately 17 to 30 km altitude) relative to simultaneously measured values of the long-lived tracer N2O. Exponential rates of increase inferred for 1985-to 1994 from these comparisons are (0.1 plus or minus 0.4)% yr(exp-1) for OCS, (1.0 plus or minus 1.0)% yr(exp-1) for HCN, (8.0 +/- 0.7)% yr(exp-1) for SF6, and (8.0 +/- 1.0)% yr(exp-1) for CHClF2 (HCFC-22), 1 sigma. The lack of an appreciable trend for OCS suggests the background (i.e. nonvolcanic) source of stratospheric aerosol was the same during the two periods. These results are compared with trends reported in the literature.
Titan's organic haze is potentially an important sink of photochemically produced carbon and nitrogen compounds. An assortment of microphysical haze models all suggest that the haze production rate is 10(exp -14) gm per square centimeter per second, within a factor of two. Spectral analysis of laboratory tholins compared to Titan's geometric albedo spectrum suggest that the laboratory material is a good analog to Titan's haze. The laboratory material has an elemental composition given approximately by C4H4N, with an uncertainty in the C/N ratio of a factor of two. Thus, the haze represents a sink for C of 4 x 10(exp 8) per square centimeter per second, and a sink for N of 1 x 10(exp 8) per square centimeter per second. The C sink is small compared to condensation of hydrocarbons but the sink for N is comparable to the total production rate of HCN. Because estimates of the eddy diffusion profile on Titan have been based on the HCN profile, inclusion of this additional sink for N will affect estimates for all transport processes in Titan's atmosphere.
The results of a study of the ion-molecule reactions of N(+), N(2)(+), and HCN(+) with methane, acetylene, and ethylene are reported. These studies were performed using the FA-SIFT at the University of Canterbury. The reactions studied here are important to understanding the ion chemistry in Titan's atmosphere. N(+) and N(2)(+) are the primary ions formed by photo-ionization and electron impact in Titan's ionosphere and drive Titan's ion chemistry. It is therefore very important to know how these ions react with the principal trace neutral species in Titan's atmosphere: Methane, acetylene, and ethylene. While these reactions have been studied before the product channels have been difficult to define as several potential isobaric products make a definitive answer difficult. Mass overlap causes difficulties in making unambiguous species assignments in these systems. Two discriminators have been used in this study to resolve the mass overlap problem. They are deuterium labeling and also the differences in reactivities of each isobar with various neutral reactants. Several differences have been found from the products in previous work. The HCN(+) ion is important in both Titan's atmosphere and in the laboratory.
Hydrogen cyanide (HCN) has successfully been used as a tracer of biomassburning in the context of aircraft campaigns. We show HCN observations fromAura-TES for a major fire in Indonesia in 2006, and globally over differentseasons. We develop a fire-influence flag for TES observations and show howthis relates to enhancements of other TES products, such as PAN, carbonmonoxide, and ozone.
Water and hydrogen cyanide are two of the most common species in space and the atmosphere with the ability of binding to form dimers such as H 2 O–HCN.
Simultaneous HCN and HOH laser emission in pulsed discharge through mixture containing H, C, N and O
Plasma refractive index effects in pulsed HCN lasers, calculating stable cavity mirror curvatures constriction as function of electron density by ray matrix approach
Major amino acids released by hydrolysis of acidic and basic HCN oligomers are identified by chromatography as Gly, Asp, and diaminosuccinic acid. Smaller amounts of Ala, Ile and alpha-aminoisobutyric acid are also detected. The amino acids released did not change appreciably when the hydrolysis medium was changed from neutral to acidic or basic. The presence of both meso and d, l-diaminosuccinic acids was established by paper chromatography and on an amino acid analyzer.
Rate constants for the rotational excitation of HCN by collisions with He atoms at temperatures below 100 K were computed from first principles and are presented in tabular form. The potential energy surface was obtained by using the uniform electron gas model of Gordon and Kim (1972) and then joined smoothly to the asymptotic long-range perturbation theory potential valid at large separations. Quantum close-coupling theory was used to analyze the collision dynamics. Individual rates are believed to be accurate to within 50% above 30 K and within a factor of two below 20 K. The results should be extendable to excitation by collision with H2 and may therefore be of value in the study of interstellar clouds.
A survey of 73 sources has been made in the emission lines of N2H(+) and HCO(+), including detailed maps of four sources (Ori A, OMC-2, DR 21 OH, and NGC 6334). These data are combined with equally extensive data for HCN and CN to make a detailed study of the spatial relationship of these four species. Actual abundance ratios are shown to vary, often sharply, over small scale lengths (of the order of 1 arcmin) within the mapped sources. Excitation temperatures also vary. All four species appear to be subthermally excited. The abundance ratios and their spatial variations are interpreted in terms of ion-molecular formation and destruction processes. It is concluded that the relative abundances of CO may be considerably lower in some regions than previously believed. No evidence is found for variations in the C/O ratio over small scale lengths in Ori A. The degree of ionization of the Ori A molecular cloud may be significantly different from that of other molecular clouds.