Search Results

Bioregenerative resource recovery components for Advanced Life Support systems will need to be reliable and stable for long duration space travel. Since 1989, bioregenerative life support research at the ALS Breadboard Project has examined processing of inedible crop residues in bioreactors for recovery of nutrients for replenishment of crop hydroponic solutions. Bioreactor operation has been reliable as demonstrated by continuous operation for up to 418 days with long periods of steady state conditions. Bioreactors have demonstrated stability following unplanned, non-lethal perturbations in pH, temperature, dissolved oxygen, and inedible residue supply. In each instance, a rapid return to steady state conditions was observed.

The National Aeronautics and Space Administration (NASA) intends to continue the human exploration of outer space. Long duration missions will require the development of reliable regenerative life support processes. The intent of this paper is to define the Kennedy Space Center Controlled Ecological Life Support System (CELSS) research plan for the development and testing of three candidate biological processors for a hybrid biological and physical-chemical waste recycling system. The system would be capable of reclaiming from inedible plant biomass, human metabolic waste, and gray water those components needed for plant growth (carbon dioxide, water, and inorganic salts), while eliminating noxious compounds and maximizing system closure. We will colaborate with AMES Research Center (ARC), Johnson Space Center (JSC), and academia, to design a functional biological-based waste processing system that could be integrated with the planned Human Rated Test Facility (HRTF) at JSC.

The objectives of these experiments were two fold: 1) to determine if accepted tissue fixation procedures can be adapted for long-term storage on-board the International Space Station (ISS) and 2) to test whether they are suitable for KSC Fixation Tubes (KFTs). Three tissue fixation parameters were tested: time, temperature and sample size.Fixation time:samples are normally fixed from several minutes to several hours, but because of the duration of the UF-1 mission to ISS, the tissue will be in fixative for up to 3 months. Super dwarf wheat tissue samples were fixed in either FAA (a fixative normally used for storage of plant tissues) or a glutaraldehyde-based fixative and stored for 100 days.

Bioreactor technology for bioprocessing graywater solutions in microgravity is under development by NASA at Johnson Space Center and at major aerospace companies. Inoculum sources have been inconsistent. Startup and subsequent operation of ground-based bioreactors may have been adversely affected by this inconsistency and/or by inoculation procedures. The goal of the research reported in this paper is to develop an inoculum that will completely biodegrade Igepon T42 soap to carbon dioxide and water under anaerobic, denitrifying conditions and with process conditions set by bioreactor design requirements for microgravity operation. Potential inoculum sources from two habitats within the KSC-ALS breadboard project were developed for potential use. The effects of pH (7.2 vs. 9.0, buffered) on soap degradation by the two inocula was determined in a flask study. Nearly all of the soap was degraded at pH 7.2 while nearly none was degraded at pH 9.0. Both inocula behaved similarly.

This report describes the design, assembly, and testing of a modified, re-circulating drip flow reactor to quantify the electrical, optical, and thermal performance of solid-state ultraviolet (UV) lighting and semi-conducting photocatalyst for potable water disinfection by advanced oxidation processes. The reactor test assembly incorporates high-output UV-A Light Emitting Diodes (LEDs) with active thermal control to reject heat and generate reactive oxygen species from immobilized titanium dioxide attached to borosilicate glass in the laminar flow stream. Compared with UV-excimer and UV-mercury arc lamps, the UV-A LED system demonstrated excellent thermal stability and good electrical and optical performance.

This paper investigates error-contributing factors frequently encountered during plant starch content determinations by the widely used methodology based on the enzymatic/colorimetric determination of glucose released from enzymatic hydrolysis of starch. Due to the dynamics and variability of starch levels in plant tissues, inaccurate results were found to be associated with sampling and tissue preparation protocols. Other error-contributing factors included: (1) incomplete removal of interfering soluble sugars before starch hydrolysis, (2) non-specific hydrolysis during gelatinisation of starch granules, (3) incomplete hydrolysis of starch due to insufficient amounts of hydrolyzing enzyme, and (4) improper use of starch standards. A unified procedure that only requires 10-25 mg dry material is presented.