Journal of the Ceramic Association, Japan
Online ISSN : 1884-2119
Print ISSN : 0366-9998
ISSN-L : 0366-9998
Volume 42, Issue 499
Displaying 1-12 of 12 articles from this issue
  • Shoichiro Nagai, Yoshiomi Mikami
    1934 Volume 42 Issue 499 Pages 399-405
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    The authors, in the present report, studied on the effects ot alumina and magnesia on the solubility of soda-lime glasses in water. The brief summaries are abstracted from the original Japanese paper, as following:
    (1) Standard compositions of soda-lime glass, i.e., SiO2: 72%, CaO: 13% and Na2O: 15%, were changed in the amounts of CaO and Na2O, by fixing the amount of SiO2 nearly constant, as in the following table 1.
    Table 1. Standard Chemical Compositions of Glass
    (2) These glasses ware prepared, by mixing chemicals, i.e., CaCO3, Na2CO3, SiO2, Al2O3 and MgO, and melting in chamotte crucibles at 1400-1450°C of gas furnace. The prepared glass samples were analysed and the following results in the table 2 were obtained, which were unfortunately a little deviated from the standard compositions shown in the above table 1.
    Table 2. Chemical Compositions of Prepared Glasses
    The tow samples were added as comparative samples, the one being the laboratory beaker glass and the another being the refreshing bottle glass. The beakes glass contains very large amount of soda, and is very soluble in water as shown in the following tables.
    (3) These glass samples were crushed and sieved by the following three sieves, i.e., (1) 64meshes/cm2 sieve, (2) 144 meshes/cm2 sieve & (3) 225 meshes/cm2 sieve. Two sorts of grains, i.e., (I) grains sieved between 64 meshes/cm2 and 144 meshes/cm2 sieves, and (II) grains between 144 meshes/cm2 and 225 meshes/cm2 sieves, were used in the present studies. These grains were completely washed by absolute alcohol and desiccated.
    (4) Solubility of glass in water was tested in two ways. The first method is to treat 5g of grains and 200cc of distilled water in silver beaker for 2 hours on water bath. After the boiling the water was decanted and. titrated by 1/50-N-H2SO4 solution. The amount of titration in cc was a degree of solubility of glass, as shown in the following table 3.
    Table 3. Comparison of Solubilities of Glasses in Water tested by Atmospheric Pressure Boiling
    From these results, it is clearly observed that the glasses containing alumina are most difficultly soluble and the magnesia containing glasses are, on the contrary, most soluble in water.
    (5) The second method is the autoclave method, which was already treated and discussed (Journ. Inst. Chem., 1920, 202; W. L. Baillie and F. E. Wilson: Journ. Soc. Chem. Ind., 1921, 40, 448R; W. E. S. Turner: Journ. Soc. Glass Tech., 1922 6, 38). The sample (I) grains was taken 5g in silver crucible with 40cc distilled water and heated 2 hours in an autoclave under pressures, (1) 5atm. and ca. 153°C, (2) 10atm. and ca 180°C, (3) 15atm. and ca. 200°C, (4) 20atm. and ca. 212°C, etc., and then the dissolved water was titrated by 1/50-N-H2SO4 solution as above described. The Results were shown in the following table 4.
    Table 4. Comparison of Solubilities of Glasses in Water by Higher Pressure Heating in Autoclave
    These results are quite equal to those in the above table 3. Alumina is very effective to make glass resistive to water and magnesia is nearly equal to lime or rather worse than lime.
    The authors wish to continue the study further and report hereafter.
    Download PDF (737K)
  • Microscopic Observation of Hydration Processes
    Seiji Kondo, Toshiyoshi Yamauchi
    1934 Volume 42 Issue 499 Pages 405-411
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    The processes which take place in the hydration of pure calcium silicates when they are gauged with 1, 3, 6 and 9 times of water have thoroughly been traced up to three months under a microscope. The samples of the silicates were prepared at following temperatures as reported in Part 1: 3CaO⋅SiO2 1700°C, and 1800°C, 2CaO⋅SiO2 1700°C, 3CaO⋅2SiO2 1450°C and 1475°C, and CaO⋅SiO2 1500°C.
    (1) The hydration of 3CaO⋅SiO2 and 2CaO⋅SiO2 has occurred quicker than that hitherto reported by others. 3CaO⋅SiO2 begn to hydrate in about 4 hours. produced crystals of Ca(OH)2 in columns and hexagonal plates in 4 to 5 hours, and began to form silicic acid gel in droplets after 40 hours. 2CaO⋅SiO2 hydrated after about 40 hours producing silicic acid gel; However no crystals of Ca(OH)2 were found.
    (2) No difference has been observed between the action of water and that of lime water used in gauging.
    (3) Any decrease in the amount of water has encouraged the formation of crystal nuclei and increased number of the crystals as well as quantity of the gel.
    (4) No change has been observable with the preparations of 3CaO⋅2SiO2 and CaO.SiO2 within three months.
    Download PDF (2047K)
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 411-414
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (806K)
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 415-427
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 427-430
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (389K)
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 430-433
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (660K)
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 433-438
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (849K)
  • [in Japanese]
    1934 Volume 42 Issue 499 Pages 438-442
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (601K)
  • 1934 Volume 42 Issue 499 Pages 443-452
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (1807K)
  • 1934 Volume 42 Issue 499 Pages 452-459
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (1413K)
  • 1934 Volume 42 Issue 499 Pages 462-465
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (770K)
  • 1934 Volume 42 Issue 499 Pages 465-466
    Published: 1934
    Released on J-STAGE: April 30, 2010
    JOURNAL FREE ACCESS
    Download PDF (422K)
feedback
Top