Abstract

Five Co-modified P92-type steels with different contents of Cr, W, Mo, B, N, and Re have been examined to evaluate the effect of the chemical composition on the evolution of Laves phase during creep at 650 °C. The creep tests have been carried out at 650 °C under various applied initial stresses ranging from 80 to 200 MPa until rupture. An increase in the B and Cr contents leads to a decrease in the size and volume fraction of M23C6 carbides precipitated during tempering and an increase in their number particle density along the boundaries. In turns, this affects the amount of the nucleation sites for Laves phase during creep. The (W+Mo) content determines the diffusion growth and coarsening of Laves phase during creep. Susceptibility of Laves phase to coarsening with a high rate is caused by the large difference in Gibbs energy between fine and large particles located at the low-angle and high-angle boundaries, respectively, and can cause the creep strength breakdown. The addition of Re to the 10%Cr steel with low N and high B contents provides the slowest coarsening of Laves phase among the steels studied.

Highlights

  • Creep resistant 9–12%Cr martensitic steels are widely used as materials for fossil power plants operating at temperatures up to 620 ◦ C [1,2]

  • The fraction of the Laves phase particles located at the low-angle boundary (LAB) is higher and reaches 35% of all particles after Stage I (Figures 7–9, and Table 5) that provides an effective anchorage of a high concentration of W atoms around the nucleus located at the high-angle boundary (HAB)

  • The B content and (W+Mo) content affect the evolution of Laves phase during creep in the steels studied

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Summary

Introduction

Creep resistant 9–12%Cr martensitic steels are widely used as materials for fossil power plants operating at temperatures up to 620 ◦ C [1,2]. The stability of the tempered martensite lath structure is provided by the stability of secondary phase particles such as the boundary. The chains of Laves phase induce a high Zener drag force, preventing migration of the lath boundaries, and provide the stability of the tempered martensite lath structure under creep conditions [6,17,32], that compensates for the depletion of W and Mo atoms from the solid solution.

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