Transformations from triclinic to hexagonal birnessite at circumneutral pH induced through pH control by common biological buffers

Abstract Laboratory experiments that explore the bioprecipitation or redox transformations of layered Mn oxides commonly employ buffers, such as the HEPES and MES buffers, to maintain solution pH to near neutrality. The assumption is that holding solution pH constant does not serve as the primary control for the variety of Mn oxide produced. To test this assumption, synthetic triclinic Na-birnessite was reacted in batch experiments with a pH 7 HEPES buffer, a pH 7 MES buffer, and an unbuffered pH 7 solution for 14 days in total darkness. At the end of the experimental run, the Mn oxide solids were analyzed by conventional and synchrotron X-ray powder diffraction. These assays revealed that in the presence of the HEPES buffer, triclinic Na-birnessite completely transformed into highly crystalline hexagonal H-birnessite. In unbuffered solutions starting at pH 7 and in the presence of MES, which offers a lower buffering capacity than does HEPES, triclinic Na-birnessite partially transformed to poorly crystalline hexagonal H-birnessite. The unbuffered pH 7 solution exhibited an increase in pH to 8.03. We interpret the results to indicate that: 1) buffers can indirectly promote the transformation of triclinic Na-birnessite to hexagonal H-birnessite by serving as a source of H + , even at circumneutral pH; 2) triclinic Na-birnessite alone can stimulate hydrolysis, which in turn induces an exchange of H + for interlayer Na + ; and 3) H-birnessite and Na-birnessite operate as an acid–conjugate base pair.