赤铁矿
溶解
化学
化学工程
沉积(地质)
相(物质)
矿物学
物理化学
地质学
有机化学
沉积物
工程类
古生物学
作者
Tadao Sugimoto,Atsushi Muramatsu
标识
DOI:10.1006/jcis.1996.0660
摘要
Some ambiguity is still involved in the interpretation of the growth mechanism of monodispersed hematite (α-Fe2O3) particles in dilute FeCl3solutions. Namely, there are two entirely different proposals on this issue, viz. aggregation of preformed primary particles of α-Fe2O3itself and reprecipitation of the ionic species through dissolution of the preformed β-FeOOH particles. In order to resolve this problem, the formation process was followed in detail through TEM, Electron Diffraction, XRD, FT-IR, and ICP spectrometry along with quantitative analyses on seed effects. As a result, it has been concluded that the nuclei of the hematite particles are initially generated with the formation of β-FeOOH particles and that they are grown by deposition of the solute originally present in the solution phase and indirectly furnished from the β-FeOOH by dissolution. As the concentration of the solute is lowered by the growth of the hematite particles, they continue to grow with the solute provided mainly from the β-FeOOH in a steady-state of the dissolution of β-FeOOH and growth of α-Fe2O3. The basic formation mechanism is common to the ellipsoidal particles grown in the presence of phosphate ions and spherical particles in their absence.
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