TY - JOUR
T1 - Crystallisation of silicate glasses and melts with chemical compositions in primary phase region of gehlenite
AU - Susa, Masahiro
AU - Sasaki, Kodai
AU - Yamauchi, Takaaki
AU - Watanabe, Takashi
AU - Endo, Rie
AU - Hayashi, Miyuki
AU - Hanao, Masahito
N1 - Publisher Copyright:
© 2020 Iron and Steel Institute of Japan. All rights reserved.
PY - 2020
Y1 - 2020
N2 - Crystallisation behaviour has been investigated on samples with two compositions: (A) 42CaO-37SiO2-21Al2O3 and (B) 43CaO-27SiO2-19Al2O3-11CaF2 (all mass%). Composition (A) is within the primary phase region of gehlenite and composition (B) is just between gehlenite and cuspidine on a mass basis. Two types of sample were prepared from glassy and molten states for each composition. These samples were characterised by differential thermal analysis, X-ray diffraction analysis and electron probe microanalysis. - Crystallised samples A from glassy state: It contained gehlenite and wollastonite in the XRD profile, and in BE images gehlenite crystals grew more largely than wollastonite, suggesting that gehlenite precipitates in preference to wollastonite. - Crystallised samples B from glassy state: It contained cuspidine and gehlenite in the XRD profile. In BE images, cuspidine precipitated but gehlenite was not observed. - Crystallised samples A from molten state: It contained only gehlenite in the XRD profile, and in BE images there was dendritic gehlenite developed across the sample. - Crystallised samples B from molten state: It contained cuspidine and CaF2 as well as gehlenite in the XRD profile. In BE images, gehlenite comprised the major part, and it is likely that gehlenite crystallises in preference to cuspidine. It is also likely that the pseudo-binary system of gehlenite and cuspidine forms eutectics and that the eutectic composition is rather closer to cuspidine. Consequently, the increase in Al2O3 concentration would little affect crystallisation of the glassy portion in actual mould fluxes containing CaF2 but strongly affects crystallisation of the liquid portion.
AB - Crystallisation behaviour has been investigated on samples with two compositions: (A) 42CaO-37SiO2-21Al2O3 and (B) 43CaO-27SiO2-19Al2O3-11CaF2 (all mass%). Composition (A) is within the primary phase region of gehlenite and composition (B) is just between gehlenite and cuspidine on a mass basis. Two types of sample were prepared from glassy and molten states for each composition. These samples were characterised by differential thermal analysis, X-ray diffraction analysis and electron probe microanalysis. - Crystallised samples A from glassy state: It contained gehlenite and wollastonite in the XRD profile, and in BE images gehlenite crystals grew more largely than wollastonite, suggesting that gehlenite precipitates in preference to wollastonite. - Crystallised samples B from glassy state: It contained cuspidine and gehlenite in the XRD profile. In BE images, cuspidine precipitated but gehlenite was not observed. - Crystallised samples A from molten state: It contained only gehlenite in the XRD profile, and in BE images there was dendritic gehlenite developed across the sample. - Crystallised samples B from molten state: It contained cuspidine and CaF2 as well as gehlenite in the XRD profile. In BE images, gehlenite comprised the major part, and it is likely that gehlenite crystallises in preference to cuspidine. It is also likely that the pseudo-binary system of gehlenite and cuspidine forms eutectics and that the eutectic composition is rather closer to cuspidine. Consequently, the increase in Al2O3 concentration would little affect crystallisation of the glassy portion in actual mould fluxes containing CaF2 but strongly affects crystallisation of the liquid portion.
KW - Alumina pick-up
KW - Crystallisation
KW - Cuspidine
KW - Gehlenite
KW - High aluminium steel
KW - Mould flux
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U2 - 10.2355/isijinternational.ISIJINT-2019-266
DO - 10.2355/isijinternational.ISIJINT-2019-266
M3 - Article
AN - SCOPUS:85078537588
SN - 0915-1559
VL - 60
SP - 58
EP - 64
JO - Transactions of the Iron and Steel Institute of Japan
JF - Transactions of the Iron and Steel Institute of Japan
IS - 1
ER -