Change in Surface Property of Calcium Carbonate by Heat-treatment

  • FUJI Masayoshi
    Department of Industrial Chemistry, Faculty of Engineering, Tokyo Metropolitan University
  • ZHANE Jingping
    Department of Industrial Chemistry, Faculty of Engineering, Tokyo Metropolitan University
  • TAKEI Takashi
    Department of Industrial Chemistry, Faculty of Engineering, Tokyo Metropolitan University
  • WATANABE Tohoru
    Department of Industrial Chemistry, Faculty of Engineering, Tokyo Metropolitan University
  • CHIKAZAWA Masatoshi
    Department of Industrial Chemistry, Faculty of Engineering, Tokyo Metropolitan University
  • WATANABE Tatsuhiko
    Research and Development 3rd Department, Research and Development Center, Nittetsu Mining Co., Ltd.
  • TANABE Katsuyuki
    Research and Development 3rd Department, Research and Development Center, Nittetsu Mining Co., Ltd.

Bibliographic Information

Other Title
  • 炭酸カルシウムの加熱による表面性状の変化

Description

The surface properties of heavy and colloidal calcium carbonate heat-treated under flowing nitrogen were examined from SEM, XRD, IR, specific surface area measurements and desorbed gas analysis by using modified temperature programmed desorption method. As a result, it was suggested that the structure of heavy calcium carbonate surface was almost as same as bulk. The physisorbed water molecules on the surface were desorbed over the range of room temperature to 200°C. The remarkable surface pyrolysis of calcium carbonate occurred with degassed carbon dioxide at 500°C. On the other hand, the surface component of colloidal calcium carbonate was similar to calcium hydroxide in several surface layers. The physisorption water molecules were desorbed until 250°C. The thermal decomposition of calcium carbonate under the layer of calcium hydroxide was slightly observed at above 500°C. It was concluded that the difference of surface properties between heavy and colloidal calcium carbonate, such as desorption temperature of physisorbed water, and surface thermal decomposition mechanism, was affected by a difference of surface initial condition.

Journal

  • Inorganic Materials

    Inorganic Materials 4 (269), 330-336, 1997

    The Society of Inorganic Materials, Japan

Details 詳細情報について

  • CRID
    1390282680366829184
  • NII Article ID
    130004011686
  • DOI
    10.11451/mukimate1994.4.330
  • ISSN
    2185436X
  • Data Source
    • JaLC
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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