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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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On the colors of Jupiter's satellite Io - Irradiation of solid sulfur at 77 K

The colors of seven sulfur allotropes at 77 K have been investigated both before and after irradiation by a high-pressure mercury lamp. S8 is white at 77 K but turns intense yellow within a few minutes on irradiation through quartz or DURAN. On warming, the yellow species (presumably chain-like sulfur diradicals characterized by an absorption at 430 nm) decomposes near 260 K and polymeric sulfur (S-infinity) is formed; the sample color changes gradually to the very similar color of an S8-S-infinity mixture, resulting in no visually detectable color change with temperatures from 77 K to 260 K. This is consistent with the lack of posteclipse brightening on Io. Other sulfur forms also turn intense yellow (S7, S10), grayish yellow (S12, S20, S-infinity), or brownish yellow (S6) on irradiation at 77 K, and these colors also change to the normal colors of the starting materials on warming to 298 K. It is suggested that the yellowish features on Io are caused by the effect of solar radiation on elemental sulfur. The yellow color thus produced may subsequently be modified by deposits of SO2 frosts and volcanic ash.

Steudel, R.↗

Photo-Curing: UV Radiation curing of polymers

The Polymers Branch of the Materials Division is dedicated to the development of high-performance for a variety of applications. Areas of significant interest include high- temperature polymers, low density, and high strength insulating materials, conductive polymers, and high density polymer electrolytes. This summer our group is working diligently on a photo-curing project. There is interest in the medical community feel the need for a new and improved balloon that will be used for angioplasty (a form of heart surgery). This product should maintain flexibility but add many other properties. Like possibly further processability and resistance to infection. Our group intends on coming up with this product by using photo-enolization (or simply, photo-curing) by Diels-Alder trapping. The main objective was to synthesize a series of new polymers by Diels-Alder cycloaddition of photoenols with more elastomeric properties. Our group was responsible for performing the proper photo-curing techniques of the polymers with diacrylates and bismaleimides, synthesizing novel monomers, and evaluating experimental results. We attempted to use a diacrylate to synthesize the polymer because of previous research done within the Polymers Branch here at NASA. Most acrylates are commercially available, have more elastometric properties than a typical rigid aromatic structure has and they contain ethylene oxides in the middle of their structure that create extensive flexibility. The problem we encountered with the acrylates is that they photo chemically and thermally self polymerize and create diradicals at low temperatures; these constraints caused a lot of unnecessary side reactions. We want to promote solely, diketone polymerization because this type of polymerization has the ability to cause very elastic polymers. We chose to direct our attention towards the usage of maleimides because they are known for eliminating these unnecessary side reactions.

Inman, Christina A.↗