TY - JOUR
T1 - Solubility of nitrogen in molten CaO-SiO2-Al2O3 slags
AU - Taira, Shoichirou
AU - Utsunomiya, Noboru
AU - Yamasaki, Yasuyuki
AU - Yamaguchi, Sigenobu
AU - Nakashima, Kunihiko
AU - Tsuru, Toshiaki
AU - Mori, Katsumi
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1997
Y1 - 1997
N2 - The solubilities of nitrogen in CaO-SiO2-Al2O3 slags were measured using N2-H2 gas or silicon nitride ceramics at 1823 K. Moreover Vickers hardness of the quenched slags was measured. Based on these results, the dissolution mechanism of nitrogen into the slags was discussed. The nitride capacity measured by an equilibrium between N2-H2 gas and slag under a given partial pressure of oxygen decreased with increasing SiO2 content. This result suggested that nitrogen dissolved in the slags by exchanging reaction between oxygen ion and nitrogen. On the other hand, the nitride capacity by an equilibrium between silicon nitride ceramics and slag was 102 to 104 times larger than that from gas-slag equilibrium. Although the nitride capacity was calculated assuming that silicon nitride decomposed, it was not in agreement with that from gas-slag equilibrium. Therefore it was estimated that the dissolution mechanism of nitrogen using silicon nitride ceramics was different from that obtained by nitrogen gas. Vickers hardness of the solidified slag after silicon nitride dissolution decreased with increasing SiO2 content and this tendency was the same as the influence of silica on nitrogen solubility. This suggested that network formation in the slag was strengthened by the dissolution of silicon nitride, which was estimated to proceed with the formation of complex network between Si-N (or Al-N) and oxide.
AB - The solubilities of nitrogen in CaO-SiO2-Al2O3 slags were measured using N2-H2 gas or silicon nitride ceramics at 1823 K. Moreover Vickers hardness of the quenched slags was measured. Based on these results, the dissolution mechanism of nitrogen into the slags was discussed. The nitride capacity measured by an equilibrium between N2-H2 gas and slag under a given partial pressure of oxygen decreased with increasing SiO2 content. This result suggested that nitrogen dissolved in the slags by exchanging reaction between oxygen ion and nitrogen. On the other hand, the nitride capacity by an equilibrium between silicon nitride ceramics and slag was 102 to 104 times larger than that from gas-slag equilibrium. Although the nitride capacity was calculated assuming that silicon nitride decomposed, it was not in agreement with that from gas-slag equilibrium. Therefore it was estimated that the dissolution mechanism of nitrogen using silicon nitride ceramics was different from that obtained by nitrogen gas. Vickers hardness of the solidified slag after silicon nitride dissolution decreased with increasing SiO2 content and this tendency was the same as the influence of silica on nitrogen solubility. This suggested that network formation in the slag was strengthened by the dissolution of silicon nitride, which was estimated to proceed with the formation of complex network between Si-N (or Al-N) and oxide.
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U2 - 10.2320/jinstmet1952.61.10_1070
DO - 10.2320/jinstmet1952.61.10_1070
M3 - Article
AN - SCOPUS:0031245739
SN - 0021-4876
VL - 61
SP - 1070
EP - 1076
JO - Nippon Kinzoku Gakkaishi/Journal of the Japan Institute of Metals
JF - Nippon Kinzoku Gakkaishi/Journal of the Japan Institute of Metals
IS - 10
ER -