Journal of the Clay Science Society of Japan (in Japanese)
Online ISSN : 2186-3563
Print ISSN : 0470-6455
ISSN-L : 0470-6455
Volume 15, Issue 1
Displaying 1-3 of 3 articles from this issue
  • Kazue TAZAKI
    1975Volume 15Issue 1 Pages 3-8
    Published: June 25, 1975
    Released on J-STAGE: September 20, 2011
    JOURNAL FREE ACCESS
    Imogolite was studied by the scanning electron microscope. Imogolite which examined was separated from Kurayoshi pumice beds. The samples were dried successively in the sealed vessel at critical point of CO2. This drying method exceeds in preservation of natural surface of imogolite than that of air-drying.
    The form of imogolite was observed as fibres-like threads. The threads were curled and entangled forming nets which were piled up one above the other. The diameter of these threads ranged from 0.03 to 0.06 μm.
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  • Experimental Studies on the Genesis of Stevensite and “Hydrated Talc”(1 st Report)
    Takabumi SAKAMOTO, Shigeru SUZUKI, Ryohei OTSUKA, Naoya IMAI
    1975Volume 15Issue 1 Pages 9-22
    Published: June 25, 1975
    Released on J-STAGE: September 20, 2011
    JOURNAL FREE ACCESS
    In order to investigate the genesis of stevensite and “hydrated talc” experimentally, naturally occurring wollastonite and pectolite were treated hydrothermally with MgCl2 solution for temperatures ranging from 100°C to 200°C. The products were examined by means of X-ray diffraction, thermal analysis, infrared absorption spectroscopy and electron microscopy.
    Both wollastonite and pectolite alter to “hydrated talc” +chrysotile (200°C-350°C) and then talc+chrysotile (≥400°C). Below 150°C is formed the poorly crystallized silicate having a trioctahedral layer structure. The formation of stevensite can not be recognized under the present experimental conditions.
    Some considerations are made on the mechanism of the conversion of wollastonite and pectolite.
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  • Kazuo TORII, Masami HOTTA, Makoto ASAKA
    1975Volume 15Issue 1 Pages 23-33
    Published: June 25, 1975
    Released on J-STAGE: September 20, 2011
    JOURNAL FREE ACCESS
    The adsorption of N2, CO2, CH4, C2H6 and C3H8 in cation exchanged clinoptilolite was examined. Clinoptilolite tuff from Futatsui, Akita Pref., was used as a starting material, from which Na-, K-, Ca-and NH4-clinoptilolite were prepared by cation exchange treatment.
    Na-clinoptilolite adsorbs considerable amount of small molecules such as N2 and CO2 slowly, whereas it is able to adsorb a small amount of large molecules such as CH4, C2H5 and C3H8rapidly. This result indicates that Na-clinoptilolite has two kinds of voids with different opening size. The apparent diameter of small aperture seems to be less than 3.7Å and that of large one more than 4.3Å. It is estimated that specific surface area of the smaller void accounts for nearly 2/3 of the whole surface area.
    K-clinoptilolite adsorbs a large amount of CH4 and C2H6 very slowly, and NH4-clinoptilolite is able to adsorb them rapidly. These results indicate that the apparent diameter of the small pore is enlarged from 3.7Å to 3.8Å depending on cation exchange.
    +Studies on Utilization of Zeolite Tuff (V)
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