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1.
Demore WB  Yung YL 《Science (New York, N.Y.)》1982,217(4566):1209-1213
Photochemical processes in planetary atmospheres are strongly influenced by catalytic effects of minor constituents. Catalytic cycles in the atmospheres of Earth and Venus are closely related. For example, chlorine oxides (CIOx) act as catalysts in the two atmospheres. On Earth, they serve to convert odd oxygen (atomic oxygen and ozone) to molecular oxygen. On Venus they have a similar effect, but in addition they accelerate the reactions of atomic and molecular oxygen with carbon monoxide. The latter process occurs by a unique combination of CIOx catalysis and sulfur dioxide photosensitization. The mechanism provides an explanation for the very low extent of carbon dioxide decomposition by sunlight in the Venus atmosphere.  相似文献   

2.
Laboratory simulation and tests of the inlet sampling system and columns of the Pioneer Venus gas chromatograph show that the sensitivity to argon is not diminished after the column regeneration step, argon isotopes are not separated, oxygen and sulfur dioxide are not produced in the inlet sampling system from sulfur trioxide, and sulfur trioxide is not formed from sulfur dioxide and oxygen. Comparisons of the volatile inventory of Venus and Earth imply similar efficiencies of early outgassing but a lower efficiency for later outgassing in the case of Venus. The high oxidation state of the Venus atmosphere in the region of cloud formation may prohibit the generation of elemental sulfur particles.  相似文献   

3.
Results from the Pioneer Venus sounder probe neutral mass spectrometer indicate that there is no difference in the isotopic ratios of carbon and oxygen between Venus and Earth to within +/- 5 percent. The mixing ratio of nitrogen is 3.5(+3)(-2) percent with an isotopic ratio within 20 percent of that of Earth. The ratio of argon-36 to argon-40 is 85 percent, and the ratio of argon-38 to argon-36 is 20 percent. The mixing ratios of argon-36 and argon-40 are approximately 40 and 50 parts per million, respectively, with an error of about a factor of 2 (mainly toward a lesser amount) resulting from uncertainty in the response of the ion pump to rare gases. Hydrogen chloride cannot account for more than a few percent of the 36 mass peak, and therefore the large excess of primordial argon is a reasonable conclusion. The ratio of neon-20 to argon-36 of 0.5 +/- 0.3 is definitely terrestrial in character rather than solar. These results indicate that there is a large excess of all primordial noble gases on Venus relative to Earth. There appears to be a considerably higher abundance of sulfur compounds below 20 kilometers than in or above the main cloud layer. The 32 and 60 mass peaks show a sharp increase below 22 kilometers, indicating the possible production of sulfur and carbon oxysulfide (COS) at the expense of sulfur dioxide.  相似文献   

4.
Several lines of evidence concerning the vertical abundance profile of water in the atmosphere of Venus lead to strikingly unusual distributions (the water vapor abundance decreases sharply in the immediately vicinity of the surface) or to serious conflicts in the profiles (different infrared bands suggest water abundances that are discrepant by a factor of 2.5 to 10). These data sets can be reconciled if (i) water molecules associate with carbon dioxide and sulfur trioxide to make gaseous carbonic acid and sulfuric acid in the lower atmosphere, and (ii) the discrepant 0.94-micrometer water measurements are due to gaseous sulfuric acid, requiring it to be a somewhat stronger absorber than water vapor inthis wavelength region. A mean total water abundance of 50 +/- 20 parts per million and a near-surface free water vapor abundance of 10 +/- 4 parts per million are derived.  相似文献   

5.
From comparison of theoretical and observed microwave brightness temperatures of Venus at 1.35 centimeters, the center of a water-vapor line, we obtain an upper limit of 0.8 percent for the water-vapor mixing ratio in the lower atmosphere. This limit is consistent with the amount of water vapor detected by Venera 4, the existence of aqueous ice clouds, and a greenhouse effect caused by water vapor and carbon dioxide. The computed spectra suggest that a sensitive procedure for detection of water vapor is examination of the wavelength region between I and 1.4 centimeters.  相似文献   

6.
Pioneer Venus ultraviolet spectra from the first 5 years of operation show a decline (by more than a factor of 10) in sulfur dioxide abundance at the cloud tops and in the amount of submicron haze above the clouds. At the time of the Pioneer Venus encounter, the values for both parameters greatly exceeded earlier upper limits. However, Venus had a similar appearance in the late 1950's, implying the episodic injection of sulfur dioxide possibly caused by episodic volcanism. The amount of haze in the Venus middle atmosphere is about ten times that found in Earth's stratosphere after the most recent major volcanic eruptions, and the thermal energy required for this injection on Venus is greater by about an order of magnitude than the largest of these recent Earth eruptions and about as large as the Krakatoa eruption of 1883. The episodic behavior of sulfur dioxide implies that steady-state models of the chemistry and dynamics of cloud-top regions may be of limited use.  相似文献   

7.
Initial examination of data from the neutral mass spectrometer on the Pioneer Venus sounder probe indicates that the abundances of argon-36, argon-38, and neon-20 in the Venus atmosphere are much higher than those of the corresponding gases in Earth's atmosphere, although the abundance of radiogenic argon-40 is apparently similar for both planets. The lower atmosphere of Venus includes significant concentrations of various gaseous sulfur compounds. The inlet leak to the mass spectrometer was temporarily blocked by an apparently liquid component of the Venus clouds during passage through the dense cloud layer. Analysis of gases released during the evaporation of the droplets shows the presence of water vapor to some compound or compounds of sulfur.  相似文献   

8.
The mobilities of ions produced in electrical discharges in the presence of trace quantities of water vapor and sulfur dioxide are generally lower than those expected for simple ions. Mass spectrometric identification reveals that species composed of water vapor and sulfur dioxide molecules clustering about common atmospheric ions are formed under these conditions. The identification of these clusters provides an explanation for the effect of trace gases on the mobilities of ions.  相似文献   

9.
Data from the Pioneer Venus radar mapper, combined with measurements of wind velocity and atmospheric composition, suggest that surface erosion on Venus varies with altitude. Calcium- and magnesium-rich weathering products are produced at high altitudes by gas-solid reactions with igneous minerals, then removed into the hotter lowlands by surface winds. These fine-grained weathering products may then rereact with the lower atmosphere and buffer the composition of the observed gases carbon dioxide, water vapor, sulfur dioxide, and hydrogen fluoride in some regions of the surface. This process is a plausible mechanism for the establishment in the lowlands of a calcium-rich mineral assemblage, which had previously been found necessary for the buffering of these species.  相似文献   

10.
Near-infrared spectra of a bright and a dark thermal emission feature on the night side of Venus have been obtained from 2.2 to 2.5 micrometers (microm) at a spectral resolution of 1200 to 1500. Both bright and dark features show numerous weak absorption bands produced by CO(2), CO, water vapor, and other gases. The bright feature (hot spot) emits more radiation than the dark feature (cold spot) throughout this spectral region, but the largest contrasts occur between 2.21 and 2.32 microm, where H(2)SO(4) clouds and a weak CO(2) band provide the only known sources of extinction. The contrast decreases by 55 to 65 percent at wavelengths longer than 2.34 microm, where CO, clouds, and water vapor also absorb and scatter upwelling radiation. This contrast reduction may provide direct spectroscopic evidence for horizontal variations in the water vapor concentrations in the Venus atmosphere at levels below the cloud tops.  相似文献   

11.
Measurements of the composition, temperature, and diurnal variations of the major neutral constituents in the thermosphere of Venus are being made with a quadrupole mass spectrometer on the Pioneer Venus orbiter. Concentrations of carbon dioxide, carbon monoxide, molecular nitrogen, atomic oxygen, and helium are presented, in addition to an empirical model of the data. The concentrations of the heavy gases, carbon dioxide, carbon monoxide, and molecular nitrogen, rapidly decrease from the evening terminator toward the nightside; the concentration of atomic oxygen remains nearly constant and the helium concentration increases, an indication of a nightside bulge. The kinetic temperature inferred from scale heights drops rapidly from 230 K at the terminator to 130 K at a solar zenith angle of 120 degrees , and to 112 K at the antisolar point.  相似文献   

12.
A homogeneous system for the selective, catalytic oxidation of methane to methanol via methyl bisulfate is reported. The net reaction catalyzed by mercuric ions, Hg(II), is the oxidation of methane by concentrated sulfuric acid to produce methyl bisulfate, water, and sulfur dioxide. The reaction is efficient. At a methane conversion of 50 percent, 85 percent selectivity to methyl bisulfate ( approximately 43 percent yield; the major side product is carbon dioxide) was achieved at a molar productivity of 10(-7) mole per cubic centimeter per second and Hg(II) turnover frequency of 10(-3) per second. Separate hydrolysis of methyl bisulfate and reoxidation of the sulfur dioxide with air provides a potentially practical scheme for the oxidation of methane to methanol with molecular oxygen. The primary steps of the Hg(II)-catalyzed reaction were individually examined and the essential elements of the mechanism were identified. The Hg(II) ion reacts with methane by an electrophilic displacement mechanism to produce an observable species, CH(3)HgOSO(3)H, 1. Under the reaction conditions, 1 readily decomposes to CH(3)OSO(3)H and the reduced mercurous species, Hg(2)(2+) The catalytic cycle is completed by the reoxidation of Hg(2)(2+) with H(2)SO(4) to regenerate Hg(II) and byproducts SO(2) and H(2)O. Thallium(III), palladium(II), and the cations of platinum and gold also oxidize methane to methyl bisulfate in sulfuric acid.  相似文献   

13.
The strongest spectral features in the Venus night airglow between 3000 and 8000 angstroms are identified as the Herzberg. II (c(1)Sigma(-)(u) - X(3)Sigma(-)(a)) bands of molecular oxygen. These bands have been produced in a laboratory afterglow by the recombination of oxygen atoms in the presence of carbon dioxide molecules. It is hypothesized that the same mechanism produces this emission in the upper atmosphere of Venus.  相似文献   

14.
Several photometric measurements of Venus made from the Pioneer Venus orbiter and probes indicate that solar near-ultraviolet radiation is being absorbed throughout much of the main cloud region, but little above the clouds or within the first one or two optical depths. Radiative transfer calculations were carried out to simulate both Pioneer Venus and ground-based data for a number of proposed cloud compositions. This comparison rules out models invoking nitrogen dioxide, meteoritic material, and volatile metals as the source of the ultraviolet absorption. Models involving either small ( approximately 1 micrometer) or large ( approximately 10 micrometers) sulfur particles have some serious difficulties, while ones invoking sulfur dioxide gas appear to be promising.  相似文献   

15.
Prinn RG 《Science (New York, N.Y.)》1973,182(4117):1132-1135
It is proposed that the visible cloud deck on Venus is composed of droplets of sulfuric acid. These are formed by the very rapid photooxidation of carbonyl sulfide in the upper atmosphere. The clouds are best described as an extensive haze since the predicted particulate scale height probably exceeds the gas scale height within the layer. The predicted mixing ratio for water is 10(-6) (lower limit), and for both carbonyl sulfide and sulfur dioxide it is 10(-7) (upper limit); these are in good agreement with observations. Gaps in the layer are not possible unless the planetary scale dynamics produce cloud turnover times of less than a few days. Under these conditions the water mixing ratio could approach 10(-4) and the formation of a thin hydrochloric acid haze at high altitude above the main cloud is possible.  相似文献   

16.
The two-filter method described by Thomas and LeClare was used to investigate the effects of trace concentrations of nitric oxide and nitrogen dioxide in dry nitrogen on the diffusion coefficient of radium A (polonium-218). Charged radium A was neutralized in 10 parts per million (ppm) nitrogen dioxide in dry nitrogen, in 8.3 ppm nitric oxide in dry 92 percent nitrogen and 8 percent oxygen, and in nitrogen with 20 and 80 percent relative humidity. No neutralization was seen in dry nitrogen, dry oxygen, dry air, or 10 ppm nitric oxide in dry nitrogen. The diffusion coefficient of the neutral radium A species was found to be 0.079 square centimeters per second, regardless of the relative humidity of the nitrogen gas atmosphere. Lower values were observed for charged species.  相似文献   

17.
High pre-eruptive water contents preserved in lunar melt inclusions   总被引:1,自引:0,他引:1  
The Moon has long been thought to be highly depleted in volatiles such as water, and indeed published direct measurements of water in lunar volcanic glasses have never exceeded 50 parts per million (ppm). Here, we report in situ measurements of water in lunar melt inclusions; these samples of primitive lunar magma, by virtue of being trapped within olivine crystals before volcanic eruption, did not experience posteruptive degassing. The lunar melt inclusions contain 615 to 1410 ppm water and high correlated amounts of fluorine (50 to 78 ppm), sulfur (612 to 877 ppm), and chlorine (1.5 to 3.0 ppm). These volatile contents are very similar to primitive terrestrial mid-ocean ridge basalts and indicate that some parts of the lunar interior contain as much water as Earth's upper mantle.  相似文献   

18.
Gas emissions and the eruptions of mount st. Helens through 1982   总被引:3,自引:0,他引:3  
The monitoring of gas emissions from Mount St. Helens includes daily airborne measurements of sulfur dioxide in the volcanic plume and monthly sampling of gases from crater fumaroles. The composition of the fumarolic gases has changed slightly since 1980: the water content increased from 90 to 98 percent, and the carbon dioxide concentrations decreased from about 10 to 1 percent. The emission rates of sulfur dioxide and carbon dioxide were at their peak during July and August 1980, decreased rapidly in late 1980, and have remained low and decreased slightly through 1981 and 1982. These patterns suggest steady outgassing of a single batch of magma (with a volume of not less than 0.3 cubic kilometer) to which no significant new magma has been added since mid-1980. The gas data were useful in predicting eruptions in August 1980 and June 1981.  相似文献   

19.
Measurements in situ of the neutral composition and temperature of the thermosphere of Venus are being made with a quadrupole mass spectrometer on the Pioneer Venus orbiter. The presence of many gases, incluiding the major constituents CO(2), CO, N(2), O, and He has been confirmed. Carbon dioxide is the most abundant constituent at altitudes below about 155 kilometers in the terminator region. Above this altitude atomic oxygen is the major constituent, with O/CO(2) ratios in the upper atmosphere being greater than was commonly expected. Isotope ratios of O and C are close to terrestrial values. The temperature inferred from scale heights above 180 kilometers is about 400 K on the dayside near the evening terminator at a solar zenith angle of about 69 degrees . It decreases to about 230 K when the solar zenith angle is about 90 degrees .  相似文献   

20.
The relative amounts of primary and secondary sulfates in atmospheric aerosols and precipitation can be estimated from measurements of the stable oxygen isotope ratios. The oxygen-18 content of sulfates formed in power plant stack gases before emission into the atmosphere is significantly higher than that of sulfates formed from sulfur dioxide after emission. Results show that 20 to 30 percent of the sulfates in rain and snow at Argonne, Illinois, are of primary origin.  相似文献   

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