On the spectral reflectance and maturation darkening of lunar soils

1976 
Optical absorption and diffuse reflectance spectra were obtained for simulated lunar glasses of four different compositions, both in their as-quenched (reduced) states and following mild subsolidus oxidation. The transmission spectra, when normalized by the FeO content of the glasses, differed from one another only in the relative intensity of an unresolved band in the UV. For fixed melting conditions the strength of this band in the as-quenched glasses increased with increasing FeO, or with increasing TiO2 for a fixed FeO content. Electron spin resonance (ESR) experiments have demonstrated the absence of Fe3+ or Ti3+ and the presence of metallic iron in these materials; all other transition-group elements were excluded in preparation. The unresolved UV absorption edge in the as-quenched reduced glasses is therefore tentatively ascribed to Fe2+→Ti4+ intervalency charge transfer transitions. A similar UV edge was also produced by oxidation, leading to the conclusion that the assignment of this band would be ambiguous in the absence of an independent determination of the valence states of Fe and Ti. The relationship between the transmission spectra of polished samples and the reflectance spectra of sieved powders of the same materials is shown to be well described by the Kubelka-Munk approximation. Using this insight, it is possible to understand the spectral characteristics both of oxidation darkening of synthetic glass powders and of maturation darkening of lunar soils in terms of (1) the growth of the aforementioned charge transfer band(s) and (2) the development of opaque surface phases. It is shown that mechanism (1) is of primary importance in lunar highland materials and that mechanism (2) dominates in mare materials. The present results, coupled with previous findings, suggest that lunar soil maturation darkening may result from vitrification only if accompanied by (a) enrichment in the elements Fe and Ti, (b) changes in valence states of these elements, (c) partial crystallization of opaque phases such as iron, ilmenite or magnetite, or (d) a combination of (a), (b), and (c).
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