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At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1994

Three millimeter molecular line observations in Sagittarius B2. 1: Full synthesis mapping study of HNO, CCS, and HC(13)CCN

We present the first full synthesis maps of the small molecules HNO, CCS, and HC(13)CCN in Sgr B2. We have observed the 3.8 mm continuum, the HNO J(sub K(sub -1)K(sub 1)) = 1(sub O1)-0(sub OO), the CCS J(sub N) = 7(sub 6)-6(sub 5), and the HC(13)CCN J = 9-8 transitions in the core of the Sgr B2 molecular cloud, using the Berkeley Illinois Maryland Association (BIMA) millimeter array and the NRAO 12 m telescope. We have found that HNO exists in five major gas clumps in the Sgr B2 region, which we have labeled HNO(N), HNO(NW), HNO(E), HNO(M), and HNO(S). Of particular interest is HNO(M), a major molecular gas concentration approximately 15 sec west of Sgr B2(M) in a region of young star formation. HNO is found to be closely associated with the ionized gas and might be depleted around bright H II complexes. In general, the peak intensity of the HNO emission is found to be offset from the peak of the continuum emission. We found evidence for some chemical differentiation among the three species, HNO, CCS, and HC(13)CCN, but the abundance ratios are in fair agreement with theoretical models. Two unidentified lines, U81420 and U81518, were observed, and a previously unknown compact dust source was detected. Our HNO data indicate the presence of a rotating approximately (2.2-4.4) x 10(exp 3)solar mass gas envelope surrounding Sgr B2(N), a possible bipolar gas outflow in HNO(M), and possibly a large (approximately 4.2 x 10(exp 4)solar mass) extended rotating disk associated with HNO(S). In addition, the CCS and HC(13)CCN data approximately outline the extended component of Sgr B2 and clearly show that the southern continuum source Sgr B2(S) is actually a major molecular source as well. Consequently, the kinematics of the Sgr B2 molecular cloud is quite complex, but in moving from the northwest to south, the LSR velocity generally changes from 79 to 46 km/s.

Kuan, Yi-Jehng↗
NASA NTRS1995

The Heat of Formation of HNO

The HNO molecule is of interest in both combustion and atmospheric chemistry. For example, Guadagnini et al. have recently presented ab initio potential energy surfaces for the three lowest lying electronic states of HNO and then used these in examining several chemical reactions that take place in the combustion of nitrogen containing fuels and in the oxidation of atmospheric nitrogen. We have previously studied the ground state potential energy surface (i.e., stationary points along the HNO reversible reaction HON path), vibrational spectrum (using an accurate quartic force field), zero-point energy, and bonding of HNO using coupled-cluster ab initio methods. HNO is also very interesting because of the unique nature of its bonding characteristics. That is, the potential energy surface is very flat along the H-N bonding coordinate thereby giving unusual harmonic and fundamental vibrational frequencies, and the H-N bond energy is rather weak in comparison to other H-N bond energies. In fact, using experimental heats of formation for HNO, H, and NO, the H- bond energy is computed to be only 49.9 kcal/ mol (298 K). However, ab initio calculations of isodesmic reaction energies involving HNO, FNO, ClNO, and several other molecules have shown that there is an inconsistency in the experimental heats of formation of the XNO (X double bond H, F, and Cl) species. Hence the motivation for this study was to determine a very accurate (Delta)H(sub f, sup o) value for HNO using state-of-the-art ab initio methods. Based on many recent studies it is evident that the singles and doubles coupled-cluster method that includes a perturbational estimate of the effects of connected triple excitations, denoted CCSD(T), in conjunction with large one-particle basis sets should be reliable to better than +/- 0.8 kcal/mol for this quantity. The computational methodology is described in the next section followed by our results and discussion. Conclusions are presented in the final section.

Lee, Timothy J.↗
NASA NTRS1995

The Heat of Formation of HNO

The HNO molecule is of interest in both combustion and atmospheric chemistry. For example, Guadagnini et al. have recently presented ab initio potential energy surfaces for the three lowest lying electronic states of HNO and then used these in examining several chemical reactions that take place in the combustion of nitrogen containing fuels and in the oxidation of atmospheric nitrogen. We have previously studied the ground state potential energy surface (i.e., stationary points along the HNO rev. reaction HON path), vibrational spectrum (using an accurate quartic force field), zero-point energy, and bonding of HNO using coupled-cluster ab initio methods. HNO is also very interesting because of the unique nature of its bonding characteristics. That is, the potential energy surface is very flat along the H-N bonding coordinate thereby giving unusual harmonic and fundamental vibrational frequencies, and the H-N bond energy is rather weak in comparison to other H-N bond energies. In fact, using experimental heats of formation for HO, H, and NO, the H- bond energy is computed to be only 49.9 kcal/ mol (298 K). However, ab initio calculations of isodesmic reaction energies involving HNO, FNO, ClNO, and several other molecules have shown that there is an inconsistency in the experimental heats of formation of the XNO (X=H, F, and Cl) species. Hence the motivation for this study was to determine a very accurate(DELTA)H(sup o)(sub f) value for HNO using state of-the-art ab initio methods. Based on many recent studies it is evident that the singles and doubles coupled-cluster method that includes a perturbational estimate of the effects of connected triple excitations, denoted CCSD(T), in conjunction with large one-particle basis sets should be reliable to better than +0.8 kcal/mol for this quantity. The computational methodology is described in the next section followed by our results and discussion. Conclusions are presented in the final section.

Lee, Timothy J.↗
NASA NTRS1994

New detections of interstellar HNO at 2 and 1.2 millimeters: More N-O bonds

The 2(sub 02) to 1(sub 01) and 3(sub 03) to 2(sub 02) transitions of HNO at 163 and 244 GHz have been detected toward several molecular clouds. In conjunction with previous measurements of the 1(sub 01) to 0(sub 00) line at 81 GHz, these observations secure the identification of interstellar HNO. The 2(sub 02) to 1(sub 01) transition of this species has been detected toward NGC 2024, Sgr B2 (NW), W51M, and Dr 21 (OH), while the 3(sub 03) to 2(sub 02) line at 1.2 mm was observed only in NGC 2024. Typical column densities of HNO observed toward these sources are N(sub tot) approximately 10(exp 12) to 10(exp 14)/sq cm, corresponding to fractional abundances of f(sub HNO) approximately 10(exp -11) to 10(exp -10). These values imply NO/HNO ratios of approximately 100 to 800. Both the HNO fractional abundances and NO/HNO ratios are in reasonable agreement with predictions of ion-molecule-type models of interstellar chemistry, provided early-time calculations are used. Such behavior contrasts with that of other nitrogen compounds, whose observed abundances are best duplicated by steady-state calculations. The chemistries of HNO and NO are thus likely to be related. These observations also suggest that interstellar N-O bonds may be more common than previously thought.

Ziurys, L. M.↗
NASA NTRS1993

New 3 millimeter observations of interstellar HNO - Reinstating a discredited identification

HNO has been observed in six interstellar clouds via its 1(01)-0(00) transition at 3 mm wavelength. L134N, W33A, W51M, and DR 21 are new HNO sources. The excellent agreement between laboratory and astronomical rest frequency in L134N is important for establishing the correctness of the astronomical assignment of this line. With the exception of Ori A, every known NO source contains detectable HNO. The typical column density ratio N(tot)(NO)/N(tot)(HNO) appears to be 100-200, except for L134N (about 800) and DR 21(OH) (about 20). These new HNO results correct several misconceptions in the current literature.

Snyder, Lewis E.↗
NASA NTRS1984

Laboratory millimeter and submillimeter spectra of HNO and DNO

The identification of interstellar molecular species via the detection of one spectral line has recently become subject to close scrutiny. The radical HNO falls into the class of interstellar molecules identified in this manner. To corroborate this identification, observation of additional spectral lines is necessary. In this paper, laboratory millimeter and submillimeter wave spectra of both HNO and DNO are reported in the frequency region 150-500 GHz. Based on these spectral line measurements, models for HNO and DNO have been constructed to yield accurate frequencies for all rotational transitions of these species below 500 GHz involving J values smaller than 10. The spectral lines can be utilized by radio astronomers to confirm the identification of interstellar HNO and to search for interstellar DNO.

Sastry, K. V. L. N.↗
NASA NTRS1996

Polar Vortex Conditions During the 1995-96 Arctic Winter: MLS CL0 and HNO(sub 3)

Microwave Limb Sounder (MLS) measurements of lower stratospheric CLO and HNO(sub 3) during the 1995-96 Arctic winter are presented. The 1995-96 Arctic winter was both colder and more persistently cold than usual, leading to an enhancement in lower stratospheric CLO of greater magnitude, vertical extent, and duration than has been previously observed in the Arctic. Vortex concentrations of HNO(sub 3) in mid-December were large due to diabetic decent. Trajectory calculations indicate that localized severe depletions of gas-phase HNO(sub 3) in mid-February and early March did not arise from intrainment of midlatitude air into the vortex and were therefore probably related to polar stratospheric cloud (PSC) formation.

Microwave Limb Sounder MLS CLO HNO3↗
NASA NTRS1994

An Accurate Quartic Force Field and Vibrational Frequencies for HNO and DNO

An accurate ab initio quartic force field for HNO has been determined using the singles and doubles coupled-cluster method that includes a perturbational estimate of the effects of connected triple excitations, CCSD(T), in conjunction with the correlation consistent polarized valence triple zeta (cc-pVTZ) basis set. Improved harmonic frequencies were determined with the cc-pVQZ basis set. Fundamental vibrational frequencies were determined using a second-order perturbation theory analysis and also using variational calculations. The N-0 stretch and bending fundamentals are determined well from both vibrational analyses. The H-N stretch, however, is shown to have an unusually large anharmonic correction, and is not well determined using second-order perturbation theory. The H-N fundamental is well determined from the variational calculations, demonstrating the quality of the ab initio quartic force field. The zero-point energy of HNO that should be used in isodesmic reactions is also discussed.

Dateo, Christopher E.↗
NASA NTRS1995

Aircraft(ER-2) and Balloon In-Situ Measurements of HC1, NO(sub 2), HNO(sub 3), N(sub 2)o, and CH(sub 4) for Testing Heterogeneous Chemistry on PSC's and Sulfate Aerosols in the 1991/92 Arctic Winter

Concentrations of HC1 measured in the 1991/3 northern hemisphere lower stratosphere from the ER-2 aircraft are significantly lower than model predictions using both gas phase and heterogeneous chemistry, but are in much better agreement with model predictions for the 1994 southern hemisphere.

In-Situ Sensor (BLISS)↗