Plan for Sterilization of Voyager Capsule
Sterilization plan for Voyager capsule
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Sterilization plan for Voyager capsule
Electronic part sterilization program using ethylene tetroxide gas
Sterilization of spacecraft telecommunications system - pressure transducers, magnetic tape recorders, and magnetic core memories
Inorganic separator for use in heat sterilized, silver-zinc primary cell with space mission applications
Space probe sterilization procedures, considering heat and radiation
Luciferase denaturation prevention using vacuum and molecular sieve during sterilization temperature exposure
Dry heat effectiveness in microorganism sterilization at 105 deg C for space probe applications
Canister, originally conceived for remote sterilization of spacecraft packages, could be used terrestrially to handle samples in biologically hazardous environments. Multiwalled canister includes inner layer of pyrotechnic powder. For sterilization, electrically activated squib ignites powder, raising temperature of outer surface of canister to 230 degrees centigrade for several minutes. Thermal-buffer inner layer prevents inside temperature for exceeding 100 degrees centigrade to protect contents from damage. Samples in field hospitals and other emergency situations could also be handled by equipment.
Operating parameters of liquid propulsion systems capable of being heat sterilized in loaded condition without venting
Humans have been exploring space for more than 40 years. For all those years microorganisms have accompanied, first un-manned spacecraft/cargo and later manned vessels. Microorganisms are everywhere on Earth, could easily adapt to new environments and/or can rapidly mutate to survive in very harsh conditions. Their presence in spacecraft and cargo have caused a few inconveniences over the years of humans spaceflight, ranging from crew health, life support systems challenges and material degradation. The sterilization of spacecraft that will host humans in long duration mission would be a costly operation that will not provide a long-term solution to the microbial colonization of the vessels. As soon as a human is exposed to the spacecraft, during the mission, microorganisms will start to populate the new environment. As the hum an presence in space increases in length, the risk from the microbial load, to hardware and crew will also increase. Mitigation of this risk includes several different strategies that will include minimizing the microbial load (in numbers and diversity) and monitoring. This presentation will provide a list of the risk mitigation strategies that should be implemented during ground processing, and during the mission. It will also discuss the areas that should be discussed before an effective in-flight microbial monitoring regimen is implemented. Microbial monitoring technologies will also be presented.
Rational model for spacecraft dry heat sterilization
Sterilization considerations for Mars probe space vehicle - biological burden estimate, control, verification, and maintenance
"Sterilization" is a term applied to any process or procedure that produces a condition of sterility. Sterility is an absolute concept and refers to the destruction or removal of all life. However, when sterility as an absolute concept is applied to the sterilization of space hardware, it ceases to be operational. Absolute proof of sterility of flight hardware is impossible. Hence, for an operational approach to certification of sterility of space hardware, it is necessary to apply the probability concept. The present report is concerned with the applicability of mathematics to predict the probability of achieving sterility in a complex space hardware system. As such, this approach is concerned with the manipulation of microbiological data rather than mathematical rigor.
Review of the biological and physical factors in dry heat sterilization
Voyager spacecraft system study - system design and analysis, payload definition, lander design, spacecraft design, sterilization, and shielding
Physical, mechanical, and electrical tests to determine the effects on polymeric products after exposure to ethylene oxide-Freon 12
Microbial sampling in industrial clean rooms, hand contact contamination experiments, and evaluation of vertical laminar flow room
Heat sterilizable batteries and separator materials for planetary landing capsules