Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “Chlorofluorocarbon”

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 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1988

Global climate changes as forecast by Goddard Institute for Space Studies three-dimensional model

The global climate effects of time-dependent atmospheric trace gas and aerosol variations are simulated by NASA-Goddard's three-dimensional climate model II, which possesses 8 x 10-deg horizontal resolution, for the cases of a 100-year control run and three different atmospheric composition scenarios in which trace gas growth is respectively a continuation of current exponential trends, a reduced linear growth, and a rapid curtailment of emissions due to which net climate forcing no longer increases after the year 2000. The experiments begin in 1958, run to the present, and encompass measured or estimated changes in CO2, CH4, N2O, chlorofluorocarbons, and stratospheric aerosols. It is shown that the greenhouse warming effect may be clearly identifiable in the 1990s.

Hansen, J.↗
NASA NTRS1988

In situ northern mid-latitude observations of ClO, O3, and BrO in the wintertime lower stratosphere

In order to test photochemical theories linking chlorofluorocarbon derivatives to O3 depletion at high latitudes in the springtime, several related atmospheric species, including O3, ClO, and BrO were measured in the lower stratosphere. The flight path extended to the center of the polar jet associated with but outside of the Arctic vortex, in which the abundance of O3 was twice its midlatitude value, whereas BrO levels were five parts per trillion (pptv) by volume between 18 and 21 km, and 2.4 pptv below that altitude. The ClO mixing ratio was as much as 65 pptv at 60 N latitude at an altitude of 20 km, and was enhanced over midlatitude values by a factor of three to five at altitudes above 18 km and by as much as a factor of 40 at altitudes below 17 km. Levels of ClO and O3 were highly correlated on all measured distance scales, and both showed an abrupt change in character at 54 N latitude. The ClO abundance north of 54 N was probably caused by low NO2 levels in the flight path.

Brune, W. H.↗
NASA NTRS1988

Ozone reduction in the 1980's - A model simulation of anthropogenic and solar perturbations

An interpretation of global ozone changes deduced from satellite data obtained since 1979 is presented, based on two-dimensional model simulations. The study shows that a depletion in total ozone of the order of 2 percent and a reduction in ozone density near 40 km of 7 to 12 percent over the 1979-1986 period are consistent with the observed increase in trace gas densities (chlorofluorocarbons, methane, nitrous oxide, carbon dioxide) and the simultaneous decrease in solar activity during this period. The model also suggests that ozone variations of solar and anthropogenic origins between 1979 and 1986 were of similar magnitude but that the ozone response to trace gas emissions increases substantially with latitude while the solar signal in ozone is present lower in the atmosphere and is nearly independent of latitude.

Brasseur, Guy↗
NASA NTRS1989

Evidence for a decline in the atmospheric accumulation rate of CHClF2 (CFC-22)

CHClF2 (CFC-22) is a promising substitute for atmospheric ozone damaging, fully halogenated hydrocarbons. Atmospheric CFC-22 measurements derived from ground-based solar spectra recorded between December 1980 and May 1988 are reported which show that the CFC-22 total column increased at an average annual exponential rate of 7.8 percent + or - 1.0 percent (2 sigma). Compared with other atmospheric data, these measurements indicate that CFC-22 is increasing at a more rapid rate than either CFC-11 or CFC-12, the two most abundant chlorofluorocarbons, but that the rate of CFC-22 increase is likely to have declined over the past few years.

Rinsland, Curtis P.↗
NASA NTRS1988

The Antarctic ozone hole

Observations of Antarctic ozone levels and the discovery of a hole in the Antarctic region are examined. The effects of chlorofluorocarbons (CFCs) on the level of stratospheric ozone are analyzed. Three cycles explaining the cause of ozone depletion in the poles are proposed. A comparison of field data and proposed depletion cycles reveals that the chemical origin of the ozone hole is due to CFCs. The potential global effects of the Antarctic ozone hole are discussed.

Molina, Mario J.↗
NASA NTRS1990

Model calculations of the relative effects of CFCs and their replacements on stratospheric ozone

Because chlorine has been linked to the destruction of stratospheric ozone, the use of many fully halogenated compounds, such as the chlorofluorocarbons CFC-11 and -12, is restricted by international agreement. Hydrohalocarbons are under intensive development as replacements for CFCs. Because they contain hydrogen, these gases are susceptible to tropospheric destruction which significantly shortens their atmospheric lifetimes,. Model calculations show that chlorine-containing hydrohalocarbons have less effect on ozone, by an order of magnitude, than their regulated counterparts.

Fisher, Donald A.↗
NASA NTRS1990

Stratospheric ozone depletion and future levels of atmospheric chlorine and bromine

The rise in atmospheric chlorine levels caused by the emission of chlorofluorocarbons and other halocarbons is thought to be the main cause of the appearance of the Antarctic ozone 'hole' in the late 1970s, and the more modest ozone depletion observed over parts of the Northern Hemisphere. Atmospheric bromine, also associated with halocarbon emissions, is believed to contribute to ozone depletion. Over the next decade, further increases in these compounds are inevitable. Model calculations show that by the end of the next century, atmospheric chlorine and bromine levels may return to those prevalent before the onset of the ozone hole, but only if more stringent regulations are applied to halocarbon production than those currently proposed.

Prather, Michael J.↗
NASA NTRS1990

Ozone loss in the Arctic polar vortex inferred from high-altitude aircraft measurements

The Arctic polar vortex in winter is known to be chemically primed for ozone depletion, yet it does not exhibit the large seasonal ozone decrease that characterizes its southern counterpart. This difference may be due in part to a net flux of ozone-rich air through the Arctic vortex, which can mask ozone loss. But by using a chemically conserved tracer as a reference, significant ozone loss can be identified. This loss is found to be correlated with high levels of chlorine monoxide, suggesting that much of the decrease in ozone is caused by anthropogenic emissions of chlorofluorocarbons.

Proffitt, M. H.↗
NASA NTRS1991

Apparatus Circulates Sterilizing Gas

Apparatus circulates sterilizing gas containing ethylene oxide and chlorofluorocarbon through laboratory or medical equipment. Confines sterilizing gas, circulating it only through parts to be treated. Consists of two units. One delivers ethylene oxide/chlorofluorocarbon gas mixture and removes gas after treatment. Other warms, humidifies, and circulates gas through equipment to be treated. Process provides reliable sterilization with negligible residual toxicity from ethylene oxide. Particularly suitable for sterilization of interiors of bioreactors, heart/lung machines, dialyzers, or other equipment including complicated tubing.

Cross, John H.↗
NASA NTRS1990

Climate Impact of Solar Variability

The conference on The Climate Impact of Solar Variability, was held at Goddard Space Flight Center from April 24 to 27, 1990. In recent years they developed a renewed interest in the potential effects of increasing greenhouse gases on climate. Carbon dioxide, methane, nitrous oxide, and the chlorofluorocarbons have been increasing at rates that could significantly change climate. There is considerable uncertainty over the magnitude of this anthropogenic change. The climate system is very complex, with feedback processes that are not fully understood. Moreover, there are two sources of natural climate variability (volcanic aerosols and solar variability) added to the anthropogenic changes which may confuse our interpretation of the observed temperature record. Thus, if we could understand the climatic impact of the natural variability, it would aid our interpretation and understanding of man-made climate changes.

Schatten, Kenneth H.↗
NASA NTRS1990

What Could Be Causing Global Ozone Depletion

The reported decline trend in global ozone between 1970 and 1986 may be in part an artifact of the analysis; the trend value appears to depend on the time interval selected for analysis--in relation to the 11-year solar cycle. If so, then the decline should diminish as one approaches solar maximum and includes data from 1987 to 1990. If the decline is real, its cause could be the result of natural and human factors other than just chlorofluorocarbons.

Singer, S. Fred↗
NASA NTRS1990

Tropospheric OH and the lifetimes of hydrochlorofluorocarbons

Hydrochlorofluorocarbons (HCFCs) may be used as alternatives for the chlorofluorocarbons (CFCs). Lifetimes for the HCFCs are predicted here in two ways: integrating their loss with a global model and scaling to another compound with a better known lifetime. Both approaches are shown to yield similar results. Three-dimensional fields of modeled tropospheric OH concentrations are used to calculate lifetimes against destruction by OH for the HCFCs and other hydrogenated halocarbons. The lifetimes of various hydro-halocarbons are shown to be insensitive to possible spatial variations and seasonal cycles. It is possible to scale the HCFC lifetimes to that of methyl chloroform or methane by using a ratio of the rate coefficients for reaction with OH at an appropriate temperature, about 277 K.

Prather, Michael↗
NASA NTRS1991

Ozone depletion in the high latitude lower stratosphere - 1979-1990

Archived Stratospheric Aerosol and Gas Experiment (SAGE, SAGE II) and Solar and Backscattered Ultraviolet (SBUV) data are used to examine lower stratospheric O3 variations at 50 deg latitude in both hemispheres. These data indicate that from 1979 to 1985, 73-90 percent of the total O3 changes have occurred below approximately 25 km in altitude. Significant O3 depletions (up to 15 percent) have occurred in the partial column (127-15.8 mbar) in both hemispheres with indications of a recovery after 1985. Two-dimensional model simulations of O3 changes from 1979 to 1990 have been carried out. Comparisons with O3 data are presented. Model results suggest that by 1985, significant declines in global O3 were caused by destruction by odd nitrogen associated with long-term variations in the flux of precipitating relativistic electrons (2.6 percent); solar UV flux changes (1.8 percent); the dilution effect associated with the Antarctic O3 hole (1.2 percent); and atmospheric increases in CH4, N2O, and chlorofluorocarbons (0.4 percent). Analyses of drift-corrected SBUV and Total Ozone Mapping Spectrometer data and model calculations indicate that between 1979 and 1985, reductions of 4.3 to 4.8 percent in total column O3 averaged between 65 deg S and 65 deg N have occurred. Calculations indicate a full global O3 decline of 5.2 percent (peak-to-peak) or 6 percent (annual average) between 1979 and 1985 with a partial recovery between 1985 and 1989.

Callis, Linwood B.↗
NASA NTRS1991

Use of satellite data to constrain the model-calculated atmospheric lifetime for N2O - Implications for other trace gases

Model calculations of the zonal-mean concentrations of N2O in the upper stratosphere are presented showing that about 80 percent of N2O is removed in the stratosphere between 30 deg N and 30 deg S. A comparison of calculated N2O values with remote data on N2O concentrations obtained from Nimbus 7 SAMS instrument indicated that the two-dimensional model of Ko and Sze (1982) may have underestimated the concentration of N2O in the tropical lower stratosphere. It is concluded that the calculated lifetimes for N2O and chlorofluorocarbon-source gases could be 30 percent shorter than previously reported values.

Ko, Malcolm K. W.↗
NASA NTRS1991

Polar stratospheric clouds and ozone depletion

A review is presented of investigations into the correlation between the depletion of ozone and the formation of polar stratospheric clouds (PSCs). Satellite measurements from Nimbus 7 showed that over the years the depletion from austral spring to austral spring has generally worsened. Approximately 70 percent of the ozone above Antarctica, which equals about 3 percent of the earth's ozone, is lost during September and October. Various hypotheses for ozone depletion are discussed including the theory suggesting that chlorine compounds might be responsible for the ozone hole, whereby chlorine enters the atmosphere as a component of chlorofluorocarbons produced by humans. The three types of PSCs, nitric acid trihydrate, slowly cooling water-ice, and rapidly cooling water-ice clouds act as important components of the Antarctic ozone depletion. It is indicated that destruction of the ozone will be more severe each year for the next few decades, leading to a doubling in area of the Antarctic ozone hole.

Toon, Owen B.↗
NASA NTRS1991

Two-dimensional model calculation of fluorine-containing reservoir species in the stratosphere

Two-dimensional model calculations have been carried out of the distributions of the fluorine-containing reservoir species HF, CF2O, and CFClO. HF constitutes the largest fluorine reservoir in the stratosphere, but CF2O also makes an important contribution to the inorganic fluorine budget. CFClO amounts are most important in the tropical lower stratosphere. HF amounts increase with altitude throughout the stratosphere, while those of CF2O and CFClO fall off above their mixing ratio peaks due to photolysis. The model is in good qualitative agreement with observed vertical profiles of HF and CF2O but tends to underestimate the total column of HF. The calculated CFClO distribution is in good agreement with the very limited data. The disagreement in the HF columns is likely due to small inaccuracies in the model's treatment of lower stratospheric photolysis of chlorofluorocarbons. The model results support the suggestion that CF2O may be heterogeneously converted to HF on the surface of polar stratospheric cloud particles. The model results also suggest that the quantum yield for photolysis of CF2O is near unity.

Kaye, Jack A.↗
NASA NTRS1992

Modulating Concentration Of Hydrazine Vapor To Aid Detection

Three techniques, flow modulation, filament modulation, and reactive-filter modulation developed to obtain selective response to hydrazine or to methyl hydrazines from photoionization detector. Implemented in portable selective hydrazine detectors, useful where continuous or rapid, repetitive quantitative measurements of concentrations of vapors of these toxic substances required. Measure concentration of gaseous hydrazines in presence of other gases like cyclohexane, chlorofluorocarbons, and ammonia. Produce modulated signal, amplitude and phase indicating amount of hydrazine, monomethyl hydrazine, or 1,1-dimethyl hydrazine present in mixture. Used with such other detectors as electrochemical cells.

Stetter, Joseph R.↗