Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “Photodissociation”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 109 records · Page 6
All sourcesNASA NTRSDOE OSTI
NASA NTRS1972

Photodissociation of nitrogen dioxide by pulsed laser light at 6943 A.

Nitrogen dioxide was photodissociated using a pulsed ruby laser at 6943 A. The energy of a single photon at this wavelength was equivalent to only 57% of the dissociation energy. The mechanism proposed to account for the results was the consecutive absorption of two photons, the first resulting in a short-lived excited state. The second photon is then absorbed by the excited species resulting in dissociation.

Gerstmayr, J. W.↗
NASA NTRS1972

Photodissociation of OSCl2 in the vacuum ultraviolet - The heat of formation of SO.

The fluorescence spectra produced during the photodissociation were observed. Two excited states of SO were formed. The threshold energy of incident photons to produce one of the excited states was determined. The result is used to obtain the heat of formation of SO. No fluorescence due to molecular chlorine was observed, and the possible reasons for this are discussed.

Okabe, H.↗
NASA NTRS1972

Photodissociation of CS2 in the vacuum ultraviolet - Determination of bond dissociation energy from the lowest vibrational level of the ground state CS2.

Photolysis in the vacuum ultraviolet results almost exclusively in the production of S(super-3)P atoms, which is in apparent violation of spin conservation. The threshold energy of incident photons required to produce fluorescence was used to calculate the bond dissociation energy (from the lowest vibrational level of the ground state), and the result agrees with the value previously derived from the photoionization of CS2. The fluorescence excitation spectrum shows peaks corresponding to Rydberg series I and II, indicating that the observed photodissociation of CS2 in the vacuum ultraviolet is mainly the result of predissociation from Rydberg states. The absorption coefficient of CS2 was measured in the region of 1200 to 1400 A.

Okabe, H.↗
NASA NTRS1972

Cross sections for production of the CO(A 1 Pi)-(X 1 Sigma) fourth positive band system and O(3 S) by photodissociation of CO2

The CO(A 1 Pi) cross sections reported here, along with previously determined electron impact results, establish the basis for calculating CO fourth positive system volume emission rates in the Martian dayglow. Calculated volume emission rates in turn determine relative distribution of photon vs. electron impact as mechanisms for producing CO(A 1 Pi) in the Mars atmosphere. The smallness of the O(1304) cross section confirms previous indirect evidence that photodissociative excitation of CO2 is not an important source of O(3 S) in the upper atmosphere of Mars.

Gentieu, E. P.↗
NASA NTRS1974

Photodissociation of carbon dioxide in the Mars upper atmosphere

Calculation of the intensity of two of the emissions produced during the dissociative excitation of carbon dioxide in the upper atmosphere of Mars by solar ultraviolet radiation. The calculation tangential column emission rates of the atomic oxygen 2972-A line and the carbon monoxide Cameron bands produced by the photodissociative mechanism are found to be factors of 3 and 10, respectively, smaller than the emission rates observed by Mariner ultraviolet spectrometers.

Barth, C. A.↗
NASA NTRS1974

Extreme ultraviolet photodissociative excitation of molecular oxygen

Photodissociation processes in molecular oxygen occurring in the wavelength range from 500 to 900 A, investigated through observations of the resulting atomic fluorescence radiation, are reported. The dispersed radiation from a continuous light source was used to excite the gas, and the resulting fluorescence radiation was observed in the ultraviolet and infrared. The results obtained are compared with the dissociation cross sections derived by Matsunaga and Watanabe (1967).

Carlson, R. W.↗
NASA NTRS1974

Photodissociation quantum yields of CO2 between 1200 and 1500 A

Measurements of the photodissociation quantum yields of CO2 have been carried out using various atomic line sources between 1200 and 1500 A. The production of CO was monitored by resonance fluorescence, and the results indicate that where the CO2 absorption spectrum is continuous, the CO quantum yield is high, but where there is structure, the yield is low.

Slanger, T. G.↗
NASA NTRS1976

CO/d-3 Delta sub i to X-1 Sigma +/ fluorescence from photodissociation of CO2 by 923 A photons

Measurements of vacuum ultraviolet fluorescence from the photodissociation of CO2 by photons from a N IV line emission source at a wavelength of 923 A have revealed a second CO band system in addition to the expected emission bands. Spectra with time resolution were obtained and the fluorescence lifetime and the dependence of fluorescence intensity on CO2 pressure were measured. An analysis of this data has permitted the second band system to be identified as originating from CO(d-3 Delta sub i to X-1 Sigma +) transitions.

Phillips, E.↗
NASA NTRS1978

H Lyman-alpha emission from photodissociation of H2O

Lyman-alpha fluorescence measurements were used to study the photodissociation of water vapor to produce H(n equals 2) atoms from threshold to 500 A. The experimental threshold of 813.0 A nearly coincides with the thermodynamic limit. Excitation cross sections rise slowly from threshold to a maximum value of (1.55 plus or minus 0.12) x 10 to the -18th sq cm at about 709 A and decrease to a negligible value below 550 A. Structure in the excitation function is attributed to predissociation of Rydberg series converging to the B(overbar)B2 state of H2O(plus).

Mentall, J. E.↗
NASA NTRS1980

OH/A 2 Sigma + - X 2 Pi sub i/ yield from H2O photodissociation in 1050-1370 A

The cross section and quantum yield for the production of the OH(A 2 Sigma + - X 2 Pi sub i) emission from H2O photodissociation by synchrotron radiation in the region 1050-1370 A are determined. Measurements of the photoemission and photoabsorption cross sections obtained for incident radiation bandwidths of 2 A reveal different vibrational structures in the range 1250-1370 A, and the photoemission is attributed to the 3a1-4a1 valence and 3a1-3sa1 Rydberg transitions. Photoemission quantum yields determined from the ratio of photoemission to photoabsorption cross sections are found to increase sharply at a threshold of 1362-5 A to a peak of 11% at 1300 A, then to decrease slowly with decreasing wavelength. Implications of the results for the dissociation processes of H2O are considered.

Lee, L. C.↗
NASA NTRS1980

Photodissociation of CO2 into CO plus O/1D/

It is shown that the photodissociation of CO2(1Sigma/g/plus) into CO(X1Sigma/plus/) plus O(1D) with a quantum yield of unity is consistent with all known data on the CO2 ultraviolet absorption band between 1675 and 1400 A. Astrophysical data from the atmospheres of Mars and Venus are not inconsistent with this interpretation and cometary data seem to support it.

Delsemme, A. H.↗