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Published November 1979 | public
Journal Article

The tetravalent manganese oxides: identification, hydration, and structural relationships by infrared spectroscopy

Abstract

A compilation of the infrared powder absorption spectra of most naturally occurring tetravalent and trivalent manganese oxides is presented which is intended to serve as a basis for the spectroscopic identification of these minerals in both ordered and disordered varieties, including those too disordered for X-ray diffraction studies. A variety of synthetic manganese oxides are also included for comparison to the natural phases. The samples include: aurorite, birnessite, braunite, buserite, chalcophanite, coronadite, cryptomelane, groutite, hausmannite, hollandite, lithiophorite, maoganite, manganese(Ill) manganate(IV), manganosite, manjiroite, marokite, nsutite, partridgeite, pyrolusite, quenselite, rancieite, ramsdellite, romanechite, sodium manganese(Il,III) manganate(IV), todorokite, and woodruffite. The spectra indicate that well-ordered water occurs in ramsdellite, chalcophanite, and most romanechites. Disordered water is observed in the spectra of nsutite, hollandites, birnessite, todorokite, buserite, and rancieite. The infrared spectra of well-ordered todorokite, birnessite and rancieite differ which indicates that they possess different structures and should be regarded as distinct mineral species. Much variation is observed in the spectra of pyrolusites, nsutites, birnessites, and todorokites which is interpreted as arising from structural disorder. Spectral trends suggest that todorokite, birnessite and rancieite have layered structures.

Additional Information

© 1979 Mineralogical Society of America. Manuscript received, February 1 2, 1979; accepted for publication, June 25, 1979. We thank the following for providing samples for this study: J. S. White, Jr., Smithsonian Institution; C. G. Cunningham, U. S. Geological Survey; A. R. Kampf, Los Angeles County Museum of Natural History; R. G. Burns and V. M. Burns, Massachusetts Institute of Technology; A. J. Bauman, Jet propulsion Laboratory; G. W. Brindley, Pennsylvania State University; A. S. Corey, Pasadena City College; V. Morgan, Boron, California; L. Dalbec, Ridgecrest, California; and R. Currier, Arcadia, California. A small portion of the funding for this work was provided by the L.S.B. Leakey Foundation and the John A. McCarthy Foundation. Helpful critical reviews were provided by R. G. Burns and R. Giovanoli, Berne.

Additional details

Created:
August 22, 2023
Modified:
October 23, 2023