Dissolution Behavior of Dicalcium Silicate and Tricalcium Phosphate Solid Solution and other Phases of Steelmaking Slag in an Aqueous Solution

被引:61
作者
Teratoko, Takuya [2 ]
Maruoka, Nobuhiro [1 ]
Shibata, Hiroyuki [1 ]
Kitamura, Shin-ya [1 ]
机构
[1] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, Sendai, Miyagi 9808577, Japan
[2] Hitachi Met Ltd, Yasugi, Shimane, Japan
基金
日本学术振兴会;
关键词
Phosphorus; steelmaking slag; extraction; leaching; pH; SOLUBILITY; ELEMENTS;
D O I
10.1515/htmp-2012-0032
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Most of the phosphorus in slag forms a solid solution of dicalcium silicate (C2S) and tricalcium phosphate (C3P), and the process used to separate this solid solution from the matrix phase is the same technology used to separate P from other valuable elements such as Mn and Cr containing in the matrix phase. Although it is known that the solubility of C2S in an aqueous solution is much greater than that of C3P, the solubility of the solid solution and that of the matrix phase have yet to be investigated. To clarify the possibility of selectively extracting P from slag through a leaching process, the dissolution behaviors of the solid solution at various compositions and that of the matrix phase were investigated. The following results were obtained: The dissolution ratio of Ca to the aqueous solution at pH = 7 was close to 1.0 in the case of pure C2S and decreased greatly with increasing C3P content. The dissolution ratio of P was about 0.1 and did not change relative to the C3P content. When the ratio of C3P in the solid solution was higher than 0.3, hydroxyapatite (HAP) formation was observed in the residue. The dissolution ratio of P increased for 30 min, and after reaching the maximum value, started to decrease owing to the precipitation of HAP. The dissolution ratio of each element from a glassy slag sample (matrix phase) was lower than that from the solid solution at every pH level. In this study, the possibility to extract a solid solution containing P without dissolving the matrix phase was found through the use of an aqueous solution at pH = 7, although the dissolution ratio of P was not sufficiently high.
引用
收藏
页码:329 / 338
页数:10
相关论文
共 11 条
[1]   SUBSOLIDUS RELATIONS IN SYSTEM 2CAO.SIO2-3CAO.P2O5 [J].
FIX, W ;
HEYMANN, H ;
HEINKE, R .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1969, 52 (06) :346-&
[2]   Dissolution behavior of nutrition elements from steelmaking slag into seawater [J].
Futatsuka, T ;
Shitogiden, K ;
Miki, T ;
Nagasaka, T ;
Hino, M .
ISIJ INTERNATIONAL, 2004, 44 (04) :753-761
[3]   SOLUBILITY OF CAHPO4. 2H2O IN SYSTEM CA(OH)2-H3PO4-H2O AT 5, 15, 25, AND 37.5 DEGREES C [J].
GREGORY, TM ;
MORENO, EC ;
BROWN, WE .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS SECTION A-PHYSICS AND CHEMISTRY, 1970, A 74 (04) :461-+
[4]  
Kim S. J., 2010, P 6 EUR SLAG C UNESI, P183
[5]   Magnetic Separation of Phosphorus Enriched Phase from Multiphase Dephosphorization Slag [J].
Kubo, Hironari ;
Matsubae-Yokoyama, Kazuyo ;
Nagasaka, Tetsuya .
ISIJ INTERNATIONAL, 2010, 50 (01) :59-64
[6]  
MCDOWELL H, 1971, INORG CHEM, V10, P1638
[7]   Consideration of dissolution behavior of elements in steelmaking slag based on their stability diagram in seawater [J].
Miki, T ;
Shitogiden, K ;
Samada, Y ;
Nagasaka, T ;
Hino, M .
TETSU TO HAGANE-JOURNAL OF THE IRON AND STEEL INSTITUTE OF JAPAN, 2003, 89 (04) :388-392
[8]   Substance Flow and Stock of Chromium Associated with Cyclic Use of Steel in Japan [J].
Oda, Takafumi ;
Daigo, Ichiro ;
Matsuno, Yasunari ;
Adachi, Yoshihiro .
ISIJ INTERNATIONAL, 2010, 50 (02) :314-323
[9]  
Ono H., 1980, Tetsu-to-hagane, V66, P1317, DOI [10.2355/ tetsutohagane1955.66.9_1317, DOI 10.2355/TETSUTOHAGANE1955.66.9_1317]
[10]   Distribution of P2O5 between Solid Solution of 2CaO•SiO2-3CaO•P2O5 and Liquid Phase [J].
Pahlevani, Farshid ;
Kitamura, Shin-ya ;
Shibata, Hiroyuki ;
Maruoka, Nobuhiro .
ISIJ INTERNATIONAL, 2010, 50 (06) :822-829