Engineering topics
Publications and source records attributed to Woeller, F..
Modified solica spheres enhance chromatographic separation. Commercially available silica spheres are modified by reacting them with molecules containing isocyante and isothiocyanate groups. Applications of surface derivatized spheres that result from reaction include analysis of samples prouced by atmospheric or soil probes.
Inconsistencies and ambiguities are noted by the present consideration of Pioneer Venus and Venera atmospheric composition measurement of Venus in the context of lower atmosphere thermodynamic equilibrium. Among the scenarios projected on the basis of assumed correctness for selected data subsets, the O2 and SO2 concentrations reported by the Pioneer Venus chromatograph and the H2O concentrations reported by Venera 11 suggest that large concentrations of SO3 are present in the lower atmosphere of Venus. Such SO3 concentrations lead, however, to difficulties in explaining the atmosphere at and above the cloud tops, and in addition require specific assumptions concerning chemical reaction rates at and near the surface.
A gas chromatograph mounted in the Pioneer Venus sounder probe measured the chemical composition of the atmosphere of Venus at three altitudes. Ne, N2, O2, Ar, CO, H2O, SO2, and CO2 were measured, and upper limits set for H2, COS, H2S, CH4, Kr, N2O, C2H4, C2H6, and C3H8. Simulation studies have provided indirect evidence for sulfuric acid-like droplets and support the possibility of water vapor at altitudes of 42 and 24 km. The paper discusses the implications of these results for the origin, evolution, and present state of Venus' atmosphere.
Misidentification of two peaks from the Pioneer Venus sounder probe gas chromatograph (SPGC), also formerly known as the LGC, gave rise to quantitative errors in the abundances of oxygen, argon, and carbon monoxide. The argon abundance is estimated at 67 parts per million and that of carbon monoxide at 20 parts per million. At this time, no estimates for the oxygen abundance can be made.
The design logic, construction, function, and data processing of the Pioneer Venus Sounder Probe gas chromatograph instrument are discussed. A gas chromatograph for the analysis of the chemical composition of the lower atmosphere of Venus was included in the Sounder Probe of the Pioneer Venus mission. This paper describes the design logic of the gas chromatograph as constrained by the mission; attention is given to instrument construction, function, and data reduction.
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, that argon isotopes are not separated, that oxygen and sulfur dioxide are not produced in the inlet sampling system from sulfur trioxide, and that 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.
The first gas chromatographic analysis of the lower atmosphere of Venus is reported. Three atmospheric samples were analyzed. The third of these samples showed carbon dioxide (96.4 percent), molecular nitrogen (3.41 percent), water vapor (0.135 percent), molecular oxygen (69.3 ppm), argon (18.6 ppm), neon (4.31 ppm), and sulfur dioxide (186 ppm). The amounts of water vapor and sulfur dioxide detected are roughly compatible with the requirements of greenhouse models of the high surface temperature of Venus. The large positive gradient of sulfur dioxide, molecular oxygen, and water vapor from the cloud tops to their bottoms, as implied by Earth-based observations and these results, gives added support for the presence of major quantities of aqueous sulfuric acid in the clouds. A comparison of the inventory of inert gases found in the atmospheres of Venus, Earth, and Mars suggests that these components are due to outgassing from the planetary interiors.
The carbon suboxide thermal polymer or its irradiated product is affected by water vapor. The polymerized carbon suboxide simulates the Martian wave of darkening on the inner wall of a glass tube when humidified by passage of water vapor through the tube. The polymer was visibly darkened by the advancing vapor front. With increasing polymer thickness and/or water vapor concentration the wave of darkening similarly intensifies simulating the dark fringe in the Martian circumpolar areas. Surfaces are lightened constantly being renewed by particulate material settling from the atmosphere. It is hypothesized that light and dark areas have polymer coatings, but light areas have small particles which scatter white light more effectively and appear brighter on the surface of Mars.
The evolution of N2, Ar, O2, and CO2 from Martian soil as a function of humidity in the Gas Exchange Experiment are correlated with the mean level of water vapor in the Martian atmosphere. All but O2 are associated with desorption. The evolution of oxygen is consistent with the presence of alkaline earth and alkali metal superoxides; and their peroxides and the gamma-Fe2O3 in the soil can account for the generation of radioactive gas in the Labeled Release Experiment. The slower evolution of CO2 from both the Gas Exchange Experiment and the Labeled Release Experiment are associated with the direct oxidation of organics by gamma-Fe2O3. The Pyrolytic Release Experiment's second peak may be carbon suboxide as demonstrated by laboratory experiments. A necessary condition is that the polymer exists in the Martian soil. We ascribe the activity of the surface samples to the reaction of Martian particulates with an anhydrous CO2 atmosphere activated by uv and ionizing radiations. The surface particles are ultimately altered by exposure to small but significant amounts of water at the sites. From the working model, we have predicted the peculiar nature of the chemical entities and demonstrated that the model is justified by laboratory data. The final confirmation of this model will entail a return to Mars, but the nature and implications of this chemistry for the Martian surface is predicted to reveal even more about Mars with further simulations in the laboratory.
Evaporative injector system for capillary column gas chromatography for solutes in dilute solution
Apollo 11 lunar fines carbon compounds, examining chemical state of porphyrins, fatty and amino acids, purines, pyrimidines and carbohydrates, etc
Electric discharge reactions in mixtures of phosphine with methane, ammonia and water, obtaining biologically significant inorganic and organic phosphorus compounds
Organic synthesis by electrical discharge in simulated Jovian atmosphere, noting appearance of orange-red cyanogen-ammonia polymer nonvolatile fraction
Isothiocyanates and phenyl isocyanate reaction with hydrazinoethanol and hydrazinoethyl hydrogen sulfate
Organic compounds synthesis by electric discharges in simulated primitive atmosphere, considering mechanism for biologically significant molecules formation
Alpha aminonitriles formation by electric discharge through anhydrous methane and ammonia mixture, showing hyrolysis to amino acid as possible bearing on chemical evolution
Synthesis of organic compounds by electric discharges in simulated primitive atmospheres