Journal of the Fuel Society of Japan
Online ISSN : 2185-226X
Print ISSN : 0369-3775
ISSN-L : 0369-3775
Volume 40, Issue 10
Displaying 1-16 of 16 articles from this issue
  • [in Japanese]
    1961 Volume 40 Issue 10 Pages 738
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (294K)
  • Shunichi Kurosawa
    1961 Volume 40 Issue 10 Pages 739-746
    Published: October 20, 1961
    Released on J-STAGE: October 21, 2011
    JOURNAL FREE ACCESS
    From the geographical point of view, in Japan petroleum costs comparatively cheaper than coal.Consequently it is natural that Japan's energy centre has been shifting from coal to petroleum.On the other hand, a plan to support the coal industry should be made throughout the industrial construction of whole Japan.
    Download PDF (1605K)
  • Summary of Report of Europe Energy Policy Survey Group
    Kiyoshi Tsuchiya, Hidezo Inaba
    1961 Volume 40 Issue 10 Pages 747-753
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    This is a summary of a report of a visit to survey recent status of energy market in Germany, France, Belgium, Graeat Britain and OEEC together with the changes of energy policy.The authors published the report titled as “Energy Policy in Europe” considering the Japanese situation with special emphasis upon the counter-plan for coal critics.The Report suggests how to establish Japan's own synthetic policy for energy.
    Download PDF (1542K)
  • Makoto Niwa
    1961 Volume 40 Issue 10 Pages 754-765
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    The rate of formation of dicobalt-octacarbonyl from cobalt tricarbonyltetramer has been measured from 78°C to 112°C.The rate of formation of cobalthydrocarbonylfrom dicobalt-octacarbonyl also has been measured from 78°C to 108°C.These two reaction rates have been compared with the reaction rate of hydroformylation.It has been found that the rate of hydroformylation was much faster than these two reaction rates.
    From these reasons it must be avoided to contain these two steps in the mechanism of hydroformylation.The rate of hydroformylation varies inversely with the partial pressure of carbormonoxide, but it does not varies with total pressure when the ratio of hydrogen to carbonmonoxide is constant.These results have led to the following mechanism.
    [Co2(CO)8]⋅+RCH=CH2+H2 [Co2(CO)7⋅RCH=CH2⋅H2]+CO
    [Co2(CO)7⋅RCH=CH2⋅H2] [Co(CO)6RCH2⋅CH2CHO]
    [Co(CO)6⋅RCH2CH2CHO]+2CO→RCH2CH2CHO+[Co2(CO)8]
    The initial stepis in equillibrium and second is rate determing step.
    Download PDF (1133K)
  • Shigeru Kajiyama, Chikao Yokokawa, Yoshinobu Takegami
    1961 Volume 40 Issue 10 Pages 761-766
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    The humic acid, which was obtained from Onoura bituminous coal boiling with 1N HNO3, was hydrogenated in the presence of Raney Ni under hydrogen pressure.
    The results of chemical analysis and infra-red spectrum of the products indicate that the functional groups of humic acid are hydrogenated at the reaction temperature below 170°C, but, above 250°C, the chemical change is rather analogous to the artificial coalification process.Considering the hydrogenation process, it is concluded that the rational formula of Onoura humic acid, which was reported previously, is legitimate.
    The results of reduction humic acid with solution of sodium in liquid ammonia lead to the conclusion that the Onoura humic acid contains 0.9 atom of etheroxygen per molecular weight 604.
    Download PDF (985K)
  • Koji Ouchi
    1961 Volume 40 Issue 10 Pages 767-776
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    The gases originally occluded in coals are accumulated by the Tepler's pump in a vaccum at 150°C and analysed by mass spectrometer.In the series of saturated hydrocarbons C3 has the minimum quantity and C4-C6 have the maximam.Methane is generlly most abundant and the quantity of the hydrocarbons over C6decreases.In the course of coalification there are two maxima at 79% C and 85% C and the other two small and unclear maxima at 79% C and 88% C.An opinion is proposed, though very speculatively, concerning to the cause of the existance of maxima from the view point that the coalification is the slow carbonisation.
    Download PDF (1253K)
  • Characteristics of Ash in Senkeki
    Riichi Shioda, Hisanori Nakamura, Eiichi Sato
    1961 Volume 40 Issue 10 Pages 777-793
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Washability curve of Senseki is greatly different from that of normal bituminous coal.Floth-flotation is almost meaningless for Senseki, i.e.in the use of usual reagent most of Senseki does not float, otherwise in case of using the most active reagent Senseki of rich ash content floats more easily than that of poor one.If we conduct the de-ashing of Senseki through autoclave method using concent-rated alkali solution, and then hydrochloric acid washing, its residual ash content is more than graphite.
    The constitution of residual ash is greatly different from graphite.Graphite consists of SiO2 and Al2O3, while Senseki consists of Fe2O3 and CaO in respective ash constitution.The constitution of Senseki resembles closely to that of special ash which has changed the washability curve.
    There is very familiar part with polar substances in ash of Senseki, most part of which is largely covered with bitumens carbonized by heating of lava.It might be concluded that the best washing method is Baum jig and table cleaning rather than floth-flotation and others.
    Download PDF (2511K)
  • 1961 Volume 40 Issue 10 Pages 794
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (167K)
  • 1961 Volume 40 Issue 10 Pages 794a-795
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (339K)
  • 1961 Volume 40 Issue 10 Pages 795
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (180K)
  • 1961 Volume 40 Issue 10 Pages 795a-796
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (355K)
  • 1961 Volume 40 Issue 10 Pages 796
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (182K)
  • 1961 Volume 40 Issue 10 Pages 796a-798
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (540K)
  • 1961 Volume 40 Issue 10 Pages 798-799
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (319K)
  • 1961 Volume 40 Issue 10 Pages 799-806
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (1248K)
  • 1961 Volume 40 Issue 10 Pages 806-812
    Published: October 20, 1961
    Released on J-STAGE: February 23, 2011
    JOURNAL FREE ACCESS
    Download PDF (821K)
feedback
Top