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Nanocrystalline manganese oxide powders have been prepared at 25 °C by precipitation from Mn(NO3)2 aqueous solution. The presence and addition sequence of H2O2 significantly influence particle characteristics of the resulting manganese oxides, including crystal structure, particle size and morphology, and surface area, depending upon molar ratio of H2O2 with respect to Mn. The precipitation from preoxidized manganese solution by H2O2 results in flakelike-shaped amorphous hydrous manganese oxide (MnO2xH2O). In the absence of H2O2, on the other hand, amorphous Mn(OH)2 is obtained, and a part of Mn(OH)2 subsequently transforms into crystalline Mn3O4 by oxidation in air. Relative population of amorphous Mn(OH)2 decreases by dissolution when post-treated with H2O2. At Mn:H2O2 = 1:4, the well-defined 16-nm-sized nanocrystalline Mn3O4 with homogenous particle morphology is prepared. The treatment with excess H2O2, however, destroys crystalline Mn3O4 and leads to further oxidation of the aqueous manganese species. Under these conditions, a mixture of needlelike Mn2O3 and cubelike Mn3O4, including amorphous MnO2xH2O, is obtained.

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Grinding effects on the synthesis and sintering of cordierite were investigated. The grinding of a precursor gel derived from colloidal processing promoted the homogeneous distribution of elements in the gel, resulting in improved reactivity for the formation of cordiertie. Grinding the calcined powder enhanced the homogeneity of the resulting powder and caused the accumulation of internal energy as crystal strain; consequently, the densities of the sintered bodies increased and the optimum temperature range for sintering widened.

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