Formation process of kaolinite from amorphous calcium silicate and aluminum chloride.

  • MIYAWAKI RITSURO
    Ceramic Technology Department, Government Industrial Research Institute
  • TOMURA SHINJI
    Ceramic Technology Department, Government Industrial Research Institute
  • INUKAI KEIICHI
    Ceramic Technology Department, Government Industrial Research Institute
  • OKAZAKI MASAHARU
    Radiation Research Department, Government Industrial Research Institute
  • TORIYAMA KAZUMI
    Radiation Research Department, Government Industrial Research Institute
  • SHIBASAKI YASUO
    Ceramic Technology Department, Government Industrial Research Institute
  • KAMORI MASANOBU
    Engineering Research Association for Artificial Clay, Government Industrial Research Institute

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Description

The formation process of kaolinitc in the hydrothermal reaction of an amorphous calcium silicate with aluminum chloride was studied by XRD, IR, DTA-TG, TEM, and high-resolution solid state 29Si-MAS/NMR. The amorphous calcium silicate prepared from diatomite and calcium hydroxide was hydrothermally treated with an aluminum chloride solution in a Teflon pressure vessel at 220°C for a reaction period varying from 1 to 144 h. As the first step of the reaction, the Q2 state component of the starting material changed into an intcrmcdiate amorphous with the Q3 state. The degree of silica-polycondensation of this state is identical to that of the intermedicate phase observed in the kaolinitization from the amorphous mixture of silica and alumina. The intermediate amorphous phase was then converted directly into the crystalline kaolinite with a platy shape (the Q3 state), without forming a spherical kaolinite. The latter was observed in the reaction system started from an amorphous mixture of silica and alumina.

Journal

  • Clay Science

    Clay Science 9 (1), 21-32, 1993

    The Clay Science Society of Japan

Details 詳細情報について

  • CRID
    1390001204112080896
  • NII Article ID
    130004105246
  • DOI
    10.11362/jcssjclayscience1960.9.21
  • ISSN
    21863555
    00098574
  • Text Lang
    en
  • Data Source
    • JaLC
    • CiNii Articles
  • Abstract License Flag
    Disallowed

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