The creep deformation resistance and rupture life of high Cr ferritic steel with a tempered martensitic lath structure are critically reviewed on the basis of experimental data. Special attention is directed to the following three subjects: creep mechanism of the ferritic steel, its alloy design for further strengthening, and loss of its creep rupture strength after long-term use.The high Cr ferritic steel is characterized by its fine subgrain structure with a high density of free dislocations within the subgrains. The dislocation substructure is the most densely distributed obstacle to dislocation motion in the steel. Its recovery controls creep rate and rupture life at elevated temperatures. Improvement of creep strength of the steel requires a fine subgrain structure with a high density of free dislocations. A sufficient number of pinning particles (MX particles in subgrain interior and M 23 C 6 particles on sub-boundaries) are necessary to cancel a large driving force for recovery due to the high dislocation density. Coarsening and agglomeration of the pinning particles have to be delayed by an appropriate alloy design of the steel.Creep rupture strength of the high Cr ferritic steel decreases quickly after long-term use. A significant improvement of creep rupture strength can be achieved if we can prevent the loss of rupture strength. In the steel tempered at high temperature, enhanced recovery of the subgrain structure along grain boundaries is the cause of the premature failure and the consequent loss of rupture strength. However, the scenario is not always applicable. Further studies are needed to solve this important problem of high Cr ferritic steel. MX particles are necessary to retain a fine subgrain structure and to achieve the excellent creep strength of the high Cr ferritic steel. Strengthening mechanism of the MX particles is another important problem left unsolved.KEY WORDS: steel for elevated temperature service; creep; strengthening mechanism; alloy design; microstructure; microstructural degradation.

Creep is a time-dependent mechanism of plastic deformation, which takes place in a range of materials under low stress-that is, under stresses lower than the yield stress. Metals and alloys can be designed to withstand creep at high temperatures, usually by a process called dispersion strengthening, in which fine particles are evenly distributed throughout the matrix. For example, high-temperature creep-resistant ferritic steels achieve optimal creep strength (at 923 K) through the dispersion of yttrium oxide nanoparticles. However, the oxide particles are introduced by complicated mechanical alloying techniques and, as a result, the production of large-scale industrial components is economically unfeasible. Here we report the production of a 9 per cent Cr martensitic steel dispersed with nanometre-scale carbonitride particles using conventional processing techniques. At 923 K, our dispersion-strengthened material exhibits a time-to-rupture that is increased by two orders of magnitude relative to the current strongest creep-resistant steels. This improvement in creep resistance is attributed to a mechanism of boundary pinning by the thermally stable carbonitride precipitates. The material also demonstrates enough fracture toughness. Our results should lead to improved grades of creep-resistant steels and to the economical manufacture of large-scale steel components for high-temperature applications.

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The distributions and precipitated amounts of M 23 C 6 carbides and MX-type carbonitrides with decreasing carbon content from 0.16 to 0.002 mass pct in 9Cr-3W steel, which is used as a heatresistant steel, has been investigated. The microstructures of the steels are observed to be martensite. Distributions of precipitates differ greatly among the steels depending on carbon concentration. In the steels containing carbon at levels above 0.05 pct, M 23 C 6 carbides precipitate along boundaries and fine MX carbonitrides precipitate mainly in the matrix after tempering. In 0.002 pct C steel, there are no M 23 C 6 carbide precipitates, and instead, fine MX with sizes of 2 to 20 nm precipitate densely along boundaries. In 0.02 pct C steel, a small amount of M 23 C 6 carbides precipitate, but the sizes are quite large and the main precipitates along boundaries are MX, as with 0.002 pct C steel. A combination of the removal of any carbide whose size is much larger than that of MX-type nitrides, and the fine distributions of MX-type nitrides along boundaries, is significantly effective for the stabilization of a variety of boundaries in the martensitic 9Cr steel.

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