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Development of a new high-performance belite cement

Development of a new high-performance belite cement
新型高性能贝利特水泥的研制
批准号:
14550799
负责人:
FUKUDA Koichiro
金额:
$2.56万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003

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英文摘要
In the present research, we have obtained the following results(1) Crystallization mechanism of interstitial melts : we have found, for the first time, the occurrence of fractional crystallization in cement clinkers during cooling. This reaction, in principle, determines the chemical compositions of the crystals and melts. In the pseudobinary system Ca2SiO4(C2S)-Ca2AlFeO5, for example, C2S solid solution, Ca2A10.41Fe0.5905, and melt coexisted at temperatures between 1375 and 1635℃. At temperatures above 1375℃, the two phases of C2S(ss) and melt was stable. Accordingly, Ca2Al0.41FeO.5905 crystallize out of the melt, thus the chemical composition of the coexisting melt becomes poor in Fe2O3 component.(2) Zonal structure of calcium aluminoferrite, which records the information on the crystallization process : As the result of the fractional crystallization, the crystals of calcium aluminoferrite showed the zonal structure, the Al/(Al+Fe) values of which seadily increases from the cores toward the rims. Tricalcium aluminate solid solutions eventually crystallize out of the differentiated melt.(3) Cationic substitution of tricalcium aluminates : the chemical formula of the tricalcium aluminate doped with Na, K, Mg, Fe and Si has been developed to be (Na, K)2x(Ca, Mg)3-x-y[(Al, Fe)1-ySiy]206 (0≦x<0.158, 0≦y<0.136).(4) Effect of substituent ions on the stable phases of calcium aluminoferrite and belite : The crystal structure of calcium aluminoferrite was dependent on the Al/(Al+Fe) value (=x). with 0≦x<0.235, space group was Pcmn, while, it was Ibm2 with 0.235≦x<0.7. The starting temperature of the α' -to-βtransformation steadily decreased from 680℃ to below the ambient temperature with increasing concentration of foreign oxides.
期刊论文(33)
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会议论文
K.Fukuda, H.Matsubara: "Anisotropic Thermal Expansion of Yttrium Silicate"J.Master.Res.. 18. 1715-1722 (2003)
K.Fukuda、H.Matsubara:“硅酸钇的各向异性热膨胀”J.Master.Res.. 18. 1715-1722 (2003)
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通讯作者:
Koichiro Fukuda: "Determination of the Pcmn/Ibm2 Phase Boundary at High Temeperatures in the System Ca_2Fe_2O_5-Ca_2Al_2O_5"Journal of the American Ceramic Society. 85・5. 1300-1302 (2002)
福田晃一郎:“Ca_2Fe_2O_5-Ca_2Al_2O_5 体系中高温下 Pcmn/Ibm2 相界的测定”美国陶瓷学会杂志 85・5(2002 年)。
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Koichiro FUKUDA: "Thermal Expansion of δ-Yttrium Disilicate"Journal of the American Ceramic Society. 87. 89-92 (2004)
Koichiro FUKUDA:“δ-二硅酸钇的热膨胀”美国陶瓷学会杂志 87. 89-92 (2004)。
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Koichiro FUKUDA: "Chemical Zoning of Calcium Aluminoferrite Formed during Melt Crystalliation in CaO-SiO2-Al2O3-Fe2O3 Pseudoquaternary System"Cement and Concrete Research. (In press). (2004)
Koichiro FUKUDA:“CaO-SiO2-Al2O3-Fe2O3 准四元体系中熔融结晶过程中形成的铁铝酸钙的化学分区”水泥和混凝土研究。
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24
    Material design and developments of uniaxially oriented polycrystalline materials with multivalent cationic conductivity
    • 批准号:
      19K22051
    • 项目类别:
      Grant-in-Aid for Challenging Research (Exploratory)
    • 资助金额:
      $4.08万
    • 财政年份:
      2019
    • 负责人:
      FUKUDA Koichiro
    • 依托单位:
    Syntheses and characterization of highly grain-aligned polycrystalline materials by reactive diffusion between solids and gases
    • 批准号:
      25630281
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.58万
    • 财政年份:
      2013
    • 负责人:
      FUKUDA Koichiro
    • 依托单位:
    Elucidation of grain-alignment mechanism of ceramics polycrystals by reactive diffusion technique
    • 批准号:
      23656399
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.5万
    • 财政年份:
      2011
    • 负责人:
      FUKUDA Koichiro
    • 依托单位:
    Synthese and advanced features of new homologous layered carbides
    • 批准号:
      21360322
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.73万
    • 财政年份:
      2009
    • 负责人:
      FUKUDA Koichiro
    • 依托单位: