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Yield strength anomaly

From Wikipedia, the free encyclopedia

In materials science, the yield strength anomaly refers to materials wherein the yield strength (i.e., the stress necessary to initiate plastic yielding) increases with temperature.[1][2][3] For the majority of materials, the yield strength decreases with increasing temperature. In metals, this decrease in yield strength is due to the thermal activation of dislocation motion, resulting in easier plastic deformation at higher temperatures.[4]

In some cases, a yield strength anomaly refers to a decrease in the ductility of a material with increasing temperature, which is also opposite the trend in the majority of materials. Anomalies in ductility can be more clear, as an anomalous effect on yield strength can be obscured by its typical decrease with temperature.[5] In concert with yield strength or ductility anomalies, some materials demonstrate extrema in other temperature dependent properties, such as a minimum in ultrasonic damping, or a maximum in electrical conductivity.[6]

The yield strength anomaly in β-brass was one of the earliest discoveries such a phenomenon,[7] and several other ordered intermetallic alloys demonstrate this effect. Precipitation-hardened superalloys exhibit a yield strength anomaly over a considerable temperature range. For these materials, the yield strength shows little variation between room temperature and several hundred degrees Celsius. Eventually, a maximum yield strength is reached. For even higher temperatures, the yield strength decreases and, eventually, drops to zero when reaching the melting temperature, where the solid material transforms into a liquid. For ordered intermetallics, the temperature of the yield strength peak is roughly 50% of the absolute melting temperature.[8]

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Mechanisms

Thermally Activated Cross Slip

A number of alloys with the L12 structure (e.g., Ni3Al, Ni3Ga, Ni3Ge, Ni3Si), show yield strength anomalies.[9] The L12 structure is a derivative of the face-centered cubic crystal structure. For these alloys, the active slip system below the peak is ⟨110⟩{111} while the active system at higher temperatures is ⟨110⟩{010}. The hardening mechanism in these alloys is the cross slip of screw dislocations from (111) to (010) crystallographic planes.[10] This cross slip is thermally activated, and the screw dislocations are much less mobile on the (010) planes, so the material is strengthened as temperatures increases and more screw dislocations are in the (010) plane. A similar mechanism has been proposed for some B2 alloys that have yield strength anomalies (e.g., CuZn, FeCo, NiTi, CoHf, CoTi, CoZr).[8]

The yield strength anomaly mechanism in Ni-based superalloys is similar.[11] In these alloys, screw superdislocations undergo thermally activated cross slip onto {100} planes from {111} planes. This prevents motion of the remaining parts of the dislocations on the (111)[-101] slip system. Again, with increasing temperature, more cross-slip occurs, so dislocation motion is more hindered and yield strength increases.

Grain Boundary Precipitation

In superalloys strengthened by metal carbides, increasingly large carbide particles form preferentially at grain boundaries, preventing grain boundary sliding at high temperatures. This leads to an increase in the yield strength, and thus a yield strength anomaly.[5]

Vacancy Activated Strengthening

While FeAl is a B2 alloy, the observed yield strength anomaly in FeAl is due to another mechanism. If cross-slip were the mechanism, then the yield strength anomaly would be rate dependent, as expected for a thermally activated process. Instead, yield strength anomaly is state dependent, which is a property that is dependent on the state of the material. As a result, vacancy activated strengthening is the most widely-accepted mechanism.[12] The vacancy formation energy is low for FeAl, allowing for an unusually high concentration of vacancies in FeAl at high temperatures (2.5% at 1000C for Fe-50Al). The vacancy formed in either aluminum-rich FeAl or through heating is an aluminum vacancy.[13]

At low temperatures around 300K, the yield strength either decreases or does not change with temperature. At moderate temperatures (0.35-0.45 Tm), yield strength has been observed to increase with an increased vacancy concentration, providing further evidence for a vacancy driven strengthening mechanism.[13][8] The increase in yield strength from increased vacancy concentration is believed to be the result of dislocations being pinned by vacancies on the slip plane, causing the dislocations to bow. Then, above the peak stress temperature, vacancies can migrate as vacancy migration is easier with elevated temperatures. At those temperatures, vacancies no longer hinder dislocation motion but rather aid climb. In the vacancy strengthening model, the increased strength below the peak stress temperature is approximated as proportional to the vacancy concentration to the one-half with the vacancy concentration estimated using Maxwell-Boltzmann statistics. Thus, the strength can be estimated as , with being the vacancy formation energy and T being the absolute temperature. Above the peak stress temperature, a diffusion-assisted deformation mechanism can be used to describe strength since vacancies are now mobile and assist dislocation motion. Above the peak, the yield strength is strain rate dependent and thus, the peak yield strength is rate dependent. As a result, the peak stress temperature increases with an increased strain rate. Note, this is different than the yield strength anomaly, which is the yield strength below the peak, being rate dependent. The peak yield strength is also dependent on percent aluminum in the FeAl alloy. As the percent aluminum increases, the peak yield strength occurs at lower temperatures.[8]

The yield strength anomaly in FeAl alloys can be hidden if thermal vacancies are not minimized through a slow anneal at a relatively low temperature (~400 °C for ~5 days).[14] Further, the yield strength anomaly is not present in systems that use a very low strain rate as the peak yield strength is strain rate dependent and thus, would occur at temperatures too low to observe the yield strength anomaly. Additionally, since the formation of vacancies requires time, the peak yield strength magnitude is dependent on how long the material is held at the peak stress temperature. Also, the peak yield strength has been found not to be dependent on crystal orientation.[8]

Other mechanisms have been proposed including a cross slip mechanism similar to that for L12, dislocation decomposition into less mobile segments at jogs, dislocation pinning, climb-lock mechanism, and slip vector transition. The slip vector transition from <111> to <100>. At the peak stress temperature, the slip system changes from <111> to <100>. The change is believed to be a result of glide in <111> becoming more difficult as temperature increases due to a friction mechanism. Then, dislocations in <100> have easier movement in comparison.[15] Another mechanism combines the vacancy strengthening mechanism with dislocation decomposition. FeAl with the addition of a tertiary additive such as Mn has been shown to also exhibit the yield stress anomaly. In contrast to FeAl, however, the peak yield strength or peak stress temperature of Fe2MnAl is not dependent on strain rate and thus, may not follow the vacancy activated strengthening mechanism. Instead, there an order-strengthening mechanism has been proposed.[8]

Applications

Turbines and Jet Engines

The yield strength anomaly is exploited in the design of gas turbines and jet engines that operate at high temperatures, where the materials used are selected based on their paramount yield and creep resistance. Superalloys can withstand high temperature loads far beyond the capabilities of steels and other alloys, and allow operation at higher temperatures, which improves efficiency.[16]

Nuclear Reactors

Materials with yield strength anomalies are used in nuclear reactors due to their high temperature mechanical properties and good corrosion resistance.[5]

References

  1. ^ Liu, J.B.; Johnson, D.D.; Smirnov, A.V. (24 May 2005), "Predicting yield-stress anomalies in L12 alloys: Ni3Ge–Fe3Ge pseudo-binaries", Acta Materialia, 53 (13): 3601–3612, Bibcode:2005AcMat..53.3601L, doi:10.1016/j.actamat.2005.04.011
  2. ^ Wua, D.; Baker, I.; Munroe, P.R.; George, E.P. (February 2007), "The yield strength anomaly of single-slip-oriented Fe–Al single crystals", Intermetallics, 15 (2): 103–107, doi:10.1016/j.intermet.2006.03.007
  3. ^ Gornostyrev, Yu. N.; A. F. Maksyutov; O. Yu. Kontsevoi; A. J. Freeman; M. I. Katsnelson; A. V. Trefilov (3 March 2003), "Negative yield stress temperature anomaly and structural stability of Pt3Al", American Physical Society March Meeting 2003, American Physical Society, vol. 2003, pp. D17.009, Bibcode:2003APS..MARD17009G
  4. ^ Smallman, R. E. (4 September 2013). Modern physical metallurgy. Ngan, A. H. W. (Eighth ed.). Oxford. ISBN 978-0-08-098223-6. OCLC 858948359.{{cite book}}: CS1 maint: location missing publisher (link)
  5. ^ a b c Han, F. F.; Zhou, B. M.; Huang, H. F.; Leng, B.; Lu, Y. L.; Dong, J. S.; Li, Z. J.; Zhou, X. T. (2016-10-01). "The tensile behavior of GH3535 superalloy at elevated temperature". Materials Chemistry and Physics. 182: 22–31. doi:10.1016/j.matchemphys.2016.07.001. ISSN 0254-0584.
  6. ^ Chu, Zhaokuang; Yu, Jinjiang; Sun, Xiaofeng; Guan, Hengrong; Hu, Zhuangqi (2010-05-15). "Tensile property and deformation behavior of a directionally solidified Ni-base superalloy". Materials Science and Engineering: A. 527 (12): 3010–3014. doi:10.1016/j.msea.2010.01.051. ISSN 0921-5093.
  7. ^ Ardley, G. W.; Cottrell, Alan Howard; Mott, Nevill Francis (1953-09-22). "Yield points in brass crystals". Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences. 219 (1138): 328–340. Bibcode:1953RSPSA.219..328A. doi:10.1098/rspa.1953.0150. S2CID 137118204.
  8. ^ a b c d e f George, E.P.; Baker, I. (1998). "A model for the yield strength anomaly of Fe—Al". Philosophical Magazine A. 77 (3): 737–750. Bibcode:1998PMagA..77..737G. doi:10.1080/01418619808224080.
  9. ^ Paidar, V; Pope, D. P; Vitek, V (1984-03-01). "A theory of the anomalous yield behavior in L12 ordered alloys". Acta Metallurgica. 32 (3): 435–448. doi:10.1016/0001-6160(84)90117-2. ISSN 0001-6160.
  10. ^ Thornton, P. H.; Davies, R. G.; Johnston, T. L. (1970-01-01). "The temperature dependence of the flow stress of the γ′ phase based upon Ni3Al". Metallurgical Transactions. 1 (1): 207–218. doi:10.1007/BF02819263. ISSN 1543-1916. S2CID 137348369.
  11. ^ Geng, Peiji; Li, Weiguo; Zhang, Xianhe; Deng, Yong; Kou, Haibo; Ma, Jianzuo; Shao, Jiaxing; Chen, Liming; Wu, Xiaozhi (2017-06-05). "A theoretical model for yield strength anomaly of Ni-base superalloys at elevated temperature". Journal of Alloys and Compounds. 706: 340–343. doi:10.1016/j.jallcom.2017.02.262. ISSN 0925-8388.
  12. ^ Morris, D.G.; Muñoz-Morris, M.A. (2010-07-01). "A re-examination of the pinning mechanisms responsible for the stress anomaly in FeAl intermetallics". FEAL 2009 - 5th Discussion Meeting on the Development of Innovative Iron Aluminium Alloys. 18 (7): 1279–1284. doi:10.1016/j.intermet.2009.12.021. ISSN 0966-9795.
  13. ^ a b Jordan, J.L.; Deevi, S.C. (2003-06-01). "Vacancy formation and effects in FeAl". Intermetallics. 11 (6): 507–528. doi:10.1016/S0966-9795(03)00027-X. ISSN 0966-9795.
  14. ^ Carleton, R.; George, E. P.; Zee, R. H. (1995-01-01). "Effects of deviations from stoichiometry on the strength anomaly and fracture behavior of B-doped FeAl". Intermetallics. 3 (6): 433–441. doi:10.1016/0966-9795(94)00041-I. ISSN 0966-9795.
  15. ^ Premkumar, M.; Singh, A.K. (2011-07-01). "Strength anomaly of the B2 phase in Ti–25Al–25Zr alloy". Intermetallics. 19 (7): 1085–1088. doi:10.1016/j.intermet.2011.03.010. ISSN 0966-9795.
  16. ^ Sheng, Li-yuan; Yang, Fang; Guo, Jian-ting; Xi, Ting-fei (2014-03-01). "Anomalous yield and intermediate temperature brittleness behaviors of directionally solidified nickel-based superalloy". Transactions of Nonferrous Metals Society of China. 24 (3): 673–681. doi:10.1016/S1003-6326(14)63110-1. ISSN 1003-6326.
This page was last edited on 2 August 2022, at 11:56
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