Creep and corrosion-resistant cast alumina-forming alloys for high temperature service in industrial and petrochemical applications

1. An austenitic Ni-base cast alloy, consisting essentially of, in weight percent:

2.5 to 4.75 Al;

21 to 26 Cr;

20 to 40 Fe;

0.75 to 2.5 total of at least one element selected from

the group consisting of Nb and Ta;

0 to 0.25 Ti;

0.09 to 1.5 Si;

0 to 0.5 V;

0 to 2 Mn;

0 to 3 Cu;

0 to 2 of at least one element selected from the group consisting of Mo and W;

0 to 1 of at least one element selected from the group consisting of Zr and Hf;

0 to 0.15 Y;

0.3 to 0.55 C;

0.005 to 0.1 B;

0 to 0.05 P;

0.002 to less than 0.06 N and

balance Ni (30 to 46 Ni),

wherein the weight percent Ni is greater than the weight percent Fe, wherein the ratio Ni/(Fe+2*C) is between 1.02 and 1.067, wherein said alloy forms an external continuous scale comprising alumina, and has a stable phase FCC austenitic matrix microstructure, said austenitic matrix being essentially delta-ferrite-free and essentially BCC-phase free, consisting of one or more carbide strengthening phases, and exhibits a creep rupture lifetime of at least 200 h at 900° C. and 50 MPa.

2. The alloys of claim 1 , wherein the mass change after 2000 hours of testing in 500 hour cycles at 900° C. in Air+10% water vapor environment is ±2 mg/cm 2 .

3. The alloys of claim 1 , wherein the mass change after 2000 hours of testing in 500 hour cycles at 900° C. in Air+10% water vapor environment is ±1 mg/cm 2 .

4. The alloys of claim 1 , wherein the mass change during oxidation testing in 500 hour cycles at 1000° C. in Air+10% water vapor environment after 1000 hour testing is ±2 mg/cm 2 .

5. The alloy of claim 1 , wherein a calculated MC carbide contents after solidification are between 0.5 and 3.0 wt. %, M 23 C 6 is between 2 and 6 wt. % and M 7 C 3 is between 0 and 3 wt. % with total carbide contents between 2.0 wt. % and 12 wt. %.

6. The alloy of claim 1 , wherein a calculated equilibrium contents of MC carbide is between 0.25 and 3.0 wt. %, M 23 C 6 is between 2 and 9 wt. % with total calculated carbide equilibrium contents between 2.0 wt. % and 12.0 wt. % at 900° C.

7. The alloy of claim 1 , wherein a calculated change in M 23 C 6 contents after 900° C. exposure is between 0.2 to 6 wt. %.

8. The alloy of claim 1 , wherein a calculated change in M 23 C 6 contents after 900° C. exposure is between 0.2 to 4 wt. %.

9. The alloy of claim 1 , wherein a calculated change in M 23 C 6 contents after 900° C. exposure is between 1.2 to 4 wt. %.

10. The alloy of claim 1 , wherein the calculated change in total carbide contents after 900° C. exposure is between 0.1 to 3.0 wt. %.

11. The alloy of claim 1 , wherein the change in total carbide contents after 900° C. exposure is between 0.1 and 1.5 wt. %, for a creep rupture lifetime of at least 100 h at 900° C. and 50 MPa.

12. The alloy of claim 1 , wherein the mass change during oxidation testing in 100 hour cycles at 1100° C. in Air+10% water vapor environment after 1000 hour testing is ±2 mg/cm 2 .

13. The alloy of claim 1 , wherein the mass change during oxidation testing in 100 hour cycles at 1100° C. in Air+10% water vapor environment after 1000 hour testing is ±1 mg/cm 2 .

14. The alloy of claim 1 , wherein the creep rupture lifetime at 1150° C., 7.17 MPa are between 200 and 1500 hours.

15. The alloy of claim 1 , wherein a calculated equilibrium contents of MC carbide is between 0.25 and 3 wt. %, M 23 C 6 is between 2 and 8 wt. % with total calculated carbide equilibrium contents between 2.0 wt. % and 9.0 wt. % at 1150° C.

16. The alloy of claim 1 , wherein a calculated change in M 23 C 6 contents after 1150° C. exposure is between 0.1 and 5.0 wt. %.

17. The alloy of claim 1 , wherein the calculated change in total carbide contents after 1150° C. exposure is between 0.0 to 2 wt. %.

18. The alloy of claim 1 , wherein the mass change during oxidation testing in 100 hour cycles at 1150° C. in Air+10% water vapor environment after 1000 hour testing is ±2 mg/cm 2 .