Bi–Ca–Cu–O–Sr system

30 accepted literature values from 1 paper(s) (experimental 15, unspecified 15); 0 calculated phase diagram(s).

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Accepted values by evidence class
Evidence classValues
experimental15
unspecified15
Accepted values by property group
Property groupValues
phase transition30

Other properties

Phase transition (30)

Phase transition, Bi–Ca–Cu–O–Sr system
PropertyValueT (K)Phases / compositionClassSourceLocationQuote
Phase transition1133 K1133CaO min, exp., 0.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 21
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Phase transition1147 K114701x1 max, calc., 0.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 10
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Phase transition1148 K114801x1 max, exp., 0.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 7
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Phase transition1159 K115902x1 max, exp., 0.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 16
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Phase transition1173 K117302x1 min, calc., 0.21 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 14
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Phase transition1173 K117302x1 min, exp., 0.21 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 12
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Phase transition1183 K118323x0 max, exp., 0.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 29
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Phase transition1189 K118991150 max, calc., 0.21 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 28
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Phase transition1193 K119391150 max, exp., 0.21 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 26
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Phase transition1195 K119523x0 max, calc., 0.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 30
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Phase transition1198 K1198CaO min, calc., 0.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 24
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Phase transition1203 K120301x1 max, exp., 0.21 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 6
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Phase transition1204 K120401x1 max, calc., 0.21 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 9
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Phase transition1205 K120502x1 min, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 13
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Phase transition1210 K1210014x24 max, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 2
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Phase transition1210 K121001x1 min, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 4
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Phase transition1210 K1210CaO min, exp., 0.21 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 20
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Phase transition1215 K121502x1 min, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 11
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Phase transition1216 K1216014x24 max, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 1
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Phase transition1216 K121601x1 min, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 3
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Phase transition1219 K121991150 max, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 27
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Phase transition1223 K122302x1 max, exp., 0.21 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 15
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Phase transition1232 K123201x1 max, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 8
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Phase transition1233 K123301x1 max, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 5
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Phase transition1236 K123691150 max, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 25
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Phase transition1239 K1239CaO min, exp., 1.01 bar O2experimental[1] Hallstedt 2003
cites Margulies 1996 doi
Table 8, p. 12, row 19
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Phase transition1244 K124402x1 max, calc., 0.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 18
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Phase transition1263 K1263CaO min, calc., 0.21 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 23
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Phase transition1295 K1295CaO min, calc., 1.01 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 22
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Phase transition1299 K129902x1 max, calc., 0.21 bar O2unspecified[1] Hallstedt 2003Table 8, p. 12, row 17
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Sources

Reporting papers the values were read from (a value cited from another work names that work in its row).

  1. Bengt Hallstedt, Ludwig J. Gauckler, Revision of the thermodynamic descriptions of the Cu–O, Ag–O, Ag–Cu–O, Bi–Sr–O, Bi–Ca–O, Bi–Cu–O, Sr–Cu–O, Ca–Cu–O and Sr–Ca–Cu–O systems, Calphad 27, 177-191 (2003). doi:10.1016/s0364-5916(03)00050-6