Static properties of lungs after oxygen exposure.
Atelectatic and direct toxic effects of oxygen on human subjects
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Atelectatic and direct toxic effects of oxygen on human subjects
For manned missions to Mars to become a reality, an efficient and reliable means of obtaining oxygen from the carbon dioxide-rich atmosphere will be required. Otherwise, the high cost of transporting the oxygen needed to sustain the astronauts will severely restrict the expedition to the martian surface. Recently, the use of electrochemical devices has been explored as a means of obtaining oxygen from the carbon dioxide-rich atmosphere. In these devices, oxygen ions diffuse through solid oxide membranes, thus, separating oxygen from the other gases presented. This phenomenon has only recently been explored as a means of obtaining large quantities of oxygen from toxic atmospheres, although first observed by Walter nernst in 1899. Nernst observed that stabilized zirconia will conduct oxygen ions when an electrical potential is applied across metallic electrodes applied to the ceramic membrane. Diatomic oxygen molecules are dissociated at the positive electrode/electrolyte interface. The oxygen ions enter the ceramic body due to the ion density gradient which is produced by the electrical potential across the electrolytic membrane. Once the ions have diffused through the membrane, they reform diatomic oxygen molecules at the anode. The separation of oxygen from carbon dioxide is achieved by the combination of thermal and electrochemical processes. The thermal decomposition of carbon dioxide (at 1000 C) results in the production of carbon monoxide and oxygen by the reaction.
One likely cause of polymer ignition in a high-pressure oxygen system is adiabatic-compression heating of polymers caused by pneumatic impact. Oxidative _ pyrolysis or combustion of polymers in a high-pressure oxygen system could generate toxic gases. This paper reports the preliminary results of toxic combustion product testing of selected polymers in a pneumatic-impact test system. Five polymers commonly used in high-pressure oxygen systems, Nylon 6/6, polychlorotrifluoroethylene (CTFE), polytetrafluoroethylene (PTFE), fluoroelastomer (Viton(TradeMark) A), and nitrile rubber (Buna N), were tested in a pneumatic-impact test system at 2500- or 3500-psia oxygen pressure. The polymers were ignited and burned, then combustion products were collected in a stainless-steel sample bottle and analyzed by GC/MS/IRD, GC/FID, and GC/Methanizer/FID. The results of adiabatic-compression tests show that combustion of hydrocarbon polymers, nitrogen-containing polymers, and halogenated polymers in high-pressure oxygen systems are relatively complete. Toxicity of the combustion product gas is presumably much lower than the combustion product gas generated from ambient-pressure oxygen (or air) environments. The NASA-Lewis equilibrium code was used to determine the composition of combustion product gas generated from a simulated, adiabatic-compression test of nine polymers. The results are presented and discussed.
Continuing efforts to improve the University of San Francisco/NASA toxicity screening test method have included the addition of exercise wheels to provide a different measure of incapacitation, and oxygen replenishment to offset any effect of oxygen depletion by the test animals. The addition of exercise wheels limited the number of animals in each test and doubled the required number of tests without any significant improvement in reproducibility. Oxygen replenishment appears to have an effect on survival in the last 5 minutes of the 30-minute test, but the effect is expected to be similar for most materials.
Clinical physiological effect of exposure to atmosphere of increased oxygen partial pressure and nitrogen
Biological effect of prolonged exposure of man and small animals to pure oxygen and helium - oxygen environment
Effects of discontinuous exposure to high oxygen low pressure environment on rats - aerospace medicine
Adsorption changes in nervous system and internal organs of mice during oxygen-induced convulsions
Physiological, psychological, and bacteriological aspects of 20 days in full pressure suits in 100 percent oxygen environment
Age dependence of resistance of chickens to 100 percent oxygen at one atm /OAP/, noting delayed mortality in adult birds
Continuous exposure of rats to 100 percent oxygen at 450 mm Hg for 64 days shows no physiological effects
Hamsters, mice and rats exposed to elevated oxygen tensions for 60-day periods with nitrogen at high or minimal levels.
Lysosomal enzymes in rats exposed to 100 percent oxygen to determine possibility of accelerated in vivo lipid peroxidation
Mortality and histopathology of germ-free rats and mice exposed to pure oxygen, noting effect of chronic respiratory condition
Acetylative capacity and lipid metabolic changes and readjustment to normality in rats in oxygen- rich environment
Pure oxygen effect on activity of lysosomal aryl sufatase in brain, liver and liver tissue homogenates from rats
Comparative pathology of animals continuously exposed to varied concentrations of carbon tetrachloride vapor in altitude chamber
Vitamins A and E deficiency effects on rats exposed to pure oxygen noting less weight gain and growth