Maraging steel

Maraging steels (a portmanteau of "martensitic" and "aging") are steels (iron alloys) that are known for possessing superior strength and toughness without losing ductility. Aging refers to the extended heat-treatment process. These steels are a special class of low-carbon ultra-high-strength steels that derive their strength not from carbon, but from precipitation of intermetallic compounds. The principal alloying element is 15 to 25 wt% nickel.[1] Secondary alloying elements, which include cobalt, molybdenum and titanium, are added to produce intermetallic precipitates.[1] Original development (by Bieber of Inco in the late 1950s) was carried out on 20 and 25 wt% Ni steels to which small additions of aluminium, titanium, and niobium were made; a rise in the price of cobalt in the late 1970s led to the development of cobalt-free maraging steels.[2]

The common, non-stainless grades contain 17–19 wt% nickel, 8–12 wt% cobalt, 3–5 wt% molybdenum and 0.2–1.6 wt% titanium. Addition of chromium produces stainless grades resistant to corrosion. This also indirectly increases hardenability as they require less nickel; high-chromium, high-nickel steels are generally austenitic and unable to transform to martensite when heat treated, while lower-nickel steels can transform to martensite. Alternative variants of nickel-reduced maraging steels are based on alloys of iron and manganese plus minor additions of aluminium, nickel and titanium where compositions between Fe-9wt% Mn to Fe-15wt% Mn have been used.[3] The manganese has a similar effect as nickel, i.e. it stabilizes the austenite phase. Hence, depending on their manganese content, Fe-Mn maraging steels can be fully martensitic after quenching them from the high temperature austenite phase or they can contain retained austenite.[4] The latter effect enables the design of maraging-TRIP steels where TRIP stands for Transformation-Induced-Plasticity.[5]

Properties

Due to the low carbon content maraging steels have good machinability. Prior to aging, they may also be cold rolled to as much as 90% without cracking. Maraging steels offer good weldability, but must be aged afterward to restore the original properties to the heat affected zone.[1]

When heat-treated the alloy has very little dimensional change, so it is often machined to its final dimensions. Due to the high alloy content maraging steels have a high hardenability. Since ductile FeNi martensites are formed upon cooling, cracks are non-existent or negligible. The steels can be nitrided to increase case hardness and polished to a fine surface finish.

Non-stainless varieties of maraging steel are moderately corrosion-resistant and resist stress corrosion and hydrogen embrittlement. Corrosion-resistance can be increased by cadmium plating or phosphating.

Grades of maraging steel

Maraging steels are usually described by a number (200, 250, 300 or 350), which indicates the approximate nominal tensile strength in thousands of pounds per square inch; the compositions and required properties are defined in MIL-S-46850D.[6] The higher grades have more cobalt and titanium in the alloy; the compositions below are taken from table 1 of MIL-S-46850D:

Maraging steel compositions
Element Grade 200 Grade 250 Grade 300 Grade 350
Ironbalancebalancebalancebalance
Nickel17.0–19.017.0–19.018.0–19.018.0–19.0
Cobalt8.0–9.07.0–8.58.5–9.511.5–12.5
Molybdenum3.0–3.54.6–5.24.6–5.24.6–5.2
Titanium0.15–0.250.3–0.50.5–0.81.3–1.6
Aluminium0.05–0.150.05–0.150.05–0.150.05–0.15
Tensile Strength (MPa)1379172420682413

That family is known as the 18Ni maraging steels, from its nickel percentage. There is also a family of cobalt-free maraging steels which are cheaper but not quite as strong; one example is Fe-18.9Ni-4.1Mo-1.9Ti. There have been Russian and Japanese research in Fe-Ni-Mn maraging alloys.[2]

Heat treatment cycle

The steel is first annealed at approximately 820 °C (1,510 °F) for 15–30 minutes for thin sections and for 1 hour per 25 mm thickness for heavy sections, to ensure formation of a fully austenitized structure. This is followed by air cooling or quenching to room temperature to form a soft, heavily dislocated iron-nickel lath (untwinned) martensite. Subsequent aging (precipitation hardening) of the more common alloys for approximately 3 hours at a temperature of 480 to 500 °C produces a fine dispersion of Ni3(X,Y) intermetallic phases along dislocations left by martensitic transformation, where X and Y are solute elements added for such precipitation. Overaging leads to a reduction in stability of the primary, metastable, coherent precipitates, leading to their dissolution and replacement with semi-coherent Laves phases such as Fe2Ni/Fe2Mo. Further excessive heat-treatment brings about the decomposition of the martensite and reversion to austenite.

Newer compositions of maraging steels have revealed other intermetallic stoichiometries and crystallographic relationships with the parent martensite, including rhombohedral and massive complex Ni50(X,Y,Z)50 (Ni50M50 in simplified notation).

Uses

Maraging steel's strength and malleability in the pre-aged stage allows it to be formed into thinner rocket and missile skins than other steels, reducing weight for a given strength.[7] Maraging steels have very stable properties and, even after overaging due to excessive temperature, only soften slightly. These alloys retain their properties at mildly elevated operating temperatures and have maximum service temperatures of over 400 °C (752 °F). They are suitable for engine components, such as crankshafts and gears, and the firing pins of automatic weapons that cycle from hot to cool repeatedly while under substantial load. Their uniform expansion and easy machinability before aging make maraging steel useful in high-wear components of assembly lines and dies. Other ultra-high-strength steels, such as AerMet alloys, are not as machinable because of their carbide content.

In the sport of fencing, blades used in competitions run under the auspices of the Fédération Internationale d'Escrime are usually made with maraging steel. Maraging blades are superior for foil and épée because crack propagation in maraging steel is 10 times slower than in carbon steel, resulting in less blade breakage and fewer injuries.[lower-roman 1][8] Stainless maraging steel is used in bicycle frames (e.g. Reynolds 953) and golf club heads.[9] It is also used in surgical components and hypodermic syringes, but is not suitable for scalpel blades because the lack of carbon prevents it from holding a good cutting edge.

American musical instrument string producer, Ernie Ball, has made a specialist type of electric guitar string out of Maraging steel, claiming that this alloy provides more output and enhanced tonal response.[10]

Maraging steel production, import and export by certain states, such as the United States,[11] is closely monitored by international authorities because it is particularly suited for use in gas centrifuges for uranium enrichment;[12] lack of maraging steel significantly hampers this process. Older centrifuges used aluminum tubes; modern ones, carbon fiber composite.

Physical properties

See also

References

  1. However, the notion that maraging steel blades break flat is a fencing urban legend. Testing has shown that the blade-breakage patterns in carbon steel and maraging steel are identical due to the similarity in the loading mode during bending. Additionally, a crack is likely to start at the same point and propagate along the same path (although much more slowly), as crack propagation in fatigue is a plastic phenomenon rather than microstructural.


  1. Degarmo, E. Paul; Black, J. T.; Kohser, Ronald A. (2003), Materials and Processes in Manufacturing (9th ed.), Wiley, p. 119, ISBN 0-471-65653-4
  2. Sha, W; Guo, Z (2009-10-26). Maraging Steels: Modelling of Microstructure, Properties and Applications. Elsevier.
  3. Raabe, D.; Sandlöbes, S.; Millan, J. J.; Ponge, D.; Assadi, H.; Herbig, M.; Choi, P.P. (2013), Segregation engineering enables nanoscale martensite to austenite phase transformation at grain boundaries: A pathway to ductile martensite, 61, Acta Materialia, pp. 6132–6152.
  4. Dmitrieva, O.; Ponge, D.; Inden, G.; Millan, J.; Choi, P.; Sietsma, J.; Raabe, D. (2011), "Chemical gradients across phase boundaries between martensite and austenite in steel studied by atom probe tomography and simulation", Acta Materialia, 59: 364–374, arXiv:1402.0232, doi:10.1016/j.actamat.2010.09.042, ISSN 1359-6454, S2CID 13781776
  5. Raabe, D.; Ponge, D.; Dmitrieva, O.; Sander, B. (2009), "Nano-precipitate hardened 1.5 GPa steels with unexpected high ductility", Scripta Materialia, 60 (12): 1141, doi:10.1016/j.scriptamat.2009.02.062
  6. Military Specification 46850D: STEEL : BAR, PLATE, SHEET, STRIP, FORGINGS, AND EXTRUSIONS, 18 PERCENT NICKEL ALLOY, MARAGING, 200 KSI, 250 KSI, 300 KSI, AND 350 KSI, HIGH QUALITY, available from http://everyspec.com/MIL-SPECS/MIL-SPECS-MIL-S/MIL-S-46850D_19899/
  7. Joby Warrick (2012-08-11). "Nuclear ruse: Posing as toymaker, Chinese merchant allegedly sought U.S. technology for Iran". The Washington Post. Retrieved 2014-02-21.
  8. Juvinall, Robert C.; Marshek, Kurt M. (2006). Fundamentals of Machine Component Design (Fourth ed.). John Wiley & Sons, Inc. p. 69. ISBN 978-0-471-66177-1.
  9. "Reynolds Technology". www.reynoldstechnology.biz. Retrieved 2020-11-13.
  10. "Slinky M-Steel Electric Guitar Strings". Ernie Ball. Retrieved 2020-07-15. Ernie Ball M-Steel Electric Guitar Strings are made of a patented Super Cobalt alloy wrapped around a Maraging steel hex core wire, producing a richer and fuller tone with a powerful low-end response.
  11. Consolidated Federal Regulations part 110--export and import of nuclear equipment and material, retrieved 2009-11-11.
  12. Patrikarakos, David (November 2012). Nuclear Iran: The Birth of an Atomic State. I.B. Tauris. p. 168. ISBN 978-1-78076-125-1.
  13. http://www.imoa.info/
  14. Ohue, Yuji; Matsumoto, Koji (10 September 2007). "Sliding–rolling contact fatigue and wear of maraging steel roller with ion-nitriding and fine particle shot-peening". Wear. 263 (1–6): 782–789. doi:10.1016/j.wear.2007.01.055.
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