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The development of a spectrophotometric analyzer for use on water samples in microgravity environments is discussed. The instrument is constructed around a commercial spectrophotometer, the Hewlett-Packard HP8453, with a separate turbidimetric analyzer, here a modified Hach 2100P ratio turbidimeter. Flow-through sample cells were constructed for each instrument to support microgravity use and sample deaeration. Spectrophotometric analyses on aqueous samples on orbit are sensitive to the presence of undissolved gases in the samples. In a micro-g environment, free gas in samples can and does remain suspended, clouding the mixture and interfering with spectral optical density measurements. This paper discusses the design of a spectrophotometric analyzer, with particular emphasis on the merits of two approaches to eliminating free gas interferences in on-orbit water analyses: hyperbaric gas redissolution and deaeration across a hydrophobic membrane.

Atmospheric monitoring is one of the most important elements in life support aboard U.S. Navy nuclear submarines. The Central Atmosphere Monitoring Systems have reliably served the U.S. Navy by accurately monitoring life gases and contaminants for nearly 30 years. However, as new knowledge of chemical effects on human health increases, the demand for monitoring additional compounds in these closed environments is also increasing. As a result, expanded capability for detecting trace compounds becomes more important and a next-generation monitoring system is warranted. In addition to improved analytical performance, the trend for submarine operation is to increase the degree of distribution and automation to minimize the resources needed for operation and maintenance. It is therefore desirable to incorporate the monitoring instrumentation into the atmosphere control system to provide real-time feedback and automated control.

Space Station Freedom presents challenges in water contamination and in the preconcentration of trace contaminants for subsequent analysis. Terrestrial methodologies for the trace level determination of mercury, alcohols, and phenols have been evaluated against levels of detection, complexity, and phase separation requirements. Microgravity compatible modifications of standard methods have been developed and tested. A total mercury sensor, employing solid phase sorption of mercury metal from the analyte followed by determination at a gold film electrode, has been breadboarded and shows a minimum level of detection of less than 0.5ppb. The system uses sodium borohydride as a reagent to facilitate mercury reduction and the decomposition of organomercury compounds. Phenols are determined using a modification of the VOC methodology previously described followed by GC/MS analysis; detection levels below 1ppb have been achieved.