2010
DOI: 10.1007/s11041-010-9239-0
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Formation of the Z-phase and prospects of martensitic steels with 11% Cr for operation above 590°c

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Cited by 26 publications
(33 citation statements)
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“…[10,11] The degradation is summarized as follows. Z phase forms in ferritic/martensitic steels containing large amounts of Cr and N, V, and Nb after long thermal exposure similar to the case for austenitic steel; [26,30] the nose temperature of Z-phase precipitation (i.e., the temperature at which precipitation occurs earliest) is 923 K (650°C); [27] the composition of Z phase is Cr(Nb,V)N, and small amounts of Fe and Si are dissolved; [27,28] a thermodynamic calculation system showed that Z phase is more stable than MX in high-Cr ferritic/martensitic steel; [30][31][32] the nucleation mechanism is not well understood, but Z phase easily nucleates on VN and Z phase is further stabilized by dissolving Nb; [32][33][34] Nb precipitates forming MX on PAGB during normalization, and Z phase is found on PAGB near Nb containing MX; [28,35,36] Z-phase particles grow and/or become coarse by collecting nearby Cr, and dissolving and consuming finely dispersed MX particles in grains [35,36] ; and a region several microns in width along and adjacent to PAGB on which coarse M 23 C 6 and Z-phase particles grow is preferentially recovered, the timing of which corresponds to an unexpected and sharp drop in strength. [10,[35][36][37] According to the previous work shown above, the unexpected drop in strength in the times to rupture and specified strain observed at 873 K (600°C) after several thousands of hours for 11Cr-2W-0.4Mo-1Cu-Nb-V steel (shown in Figures 2, 7, and 11) is considered to be mainly because of the formation of Z phase on PAGB and the resulting local and heterogeneous recovery along PAGB.…”
mentioning
confidence: 99%
“…[10,11] The degradation is summarized as follows. Z phase forms in ferritic/martensitic steels containing large amounts of Cr and N, V, and Nb after long thermal exposure similar to the case for austenitic steel; [26,30] the nose temperature of Z-phase precipitation (i.e., the temperature at which precipitation occurs earliest) is 923 K (650°C); [27] the composition of Z phase is Cr(Nb,V)N, and small amounts of Fe and Si are dissolved; [27,28] a thermodynamic calculation system showed that Z phase is more stable than MX in high-Cr ferritic/martensitic steel; [30][31][32] the nucleation mechanism is not well understood, but Z phase easily nucleates on VN and Z phase is further stabilized by dissolving Nb; [32][33][34] Nb precipitates forming MX on PAGB during normalization, and Z phase is found on PAGB near Nb containing MX; [28,35,36] Z-phase particles grow and/or become coarse by collecting nearby Cr, and dissolving and consuming finely dispersed MX particles in grains [35,36] ; and a region several microns in width along and adjacent to PAGB on which coarse M 23 C 6 and Z-phase particles grow is preferentially recovered, the timing of which corresponds to an unexpected and sharp drop in strength. [10,[35][36][37] According to the previous work shown above, the unexpected drop in strength in the times to rupture and specified strain observed at 873 K (600°C) after several thousands of hours for 11Cr-2W-0.4Mo-1Cu-Nb-V steel (shown in Figures 2, 7, and 11) is considered to be mainly because of the formation of Z phase on PAGB and the resulting local and heterogeneous recovery along PAGB.…”
mentioning
confidence: 99%
“…At rupture time ≤5000 h, in the 9Cr2W steel, the V and Cr contents were essentially independent on the rupture time. Therefore, no gradual increase in Cr content within the V-rich MX particles resulting in transformation of their cubic lattice into tetragonal lattice of Z-phase [20,32,34] was detected.…”
Section: Crept Microstructuresmentioning
confidence: 93%
“…When the particles are small, they tend to decrease the mobility of grain boundaries formed upon straining by dynamic recrystallization and during the interpass time by static and metadynamic recrystallization. In turn, when precipitates coalesce, a degradation of fatigue properties and corrosion resistance of the material is noticed [11][12][13][14][15][16]. The formation of Z-phase is unclear at present and not well established whether it is formed from prior nitride precipitates as proposed by some authors [13,[17][18][19] or directly nucleated as suggested by others [8,20,21].…”
Section: Accepted Manuscriptmentioning
confidence: 97%