Tailored thermal expansion alloys
Source abstract
Abstract
Abstract Current approaches to tailoring the thermal expansion coefficient of materials or finding materials with negative thermal expansion rely on careful manipulation of either the material's composition and/or the complex fabrication of composites. Here, by contrast, we report a new principle that enables the precise control of macroscopic thermal expansion response of bulk materials via crystallographic texture manipulation and by taking advantage of anisotropic Coefficients of Thermal Expansion (CTE) in a large class of martensitically transforming materials. Through simple thermo-mechanical processing, it is possible to tailor the thermal expansion response of a single material––without manipulating its composition––over a wide range of positive and negative values. We demonstrate this principle by gradually tuning the macroscopic CTE in a model NiTiPd alloy between a positive (+14.90 × 10−6 K−1) and a negative (−3.06 × 10−6 K−1) value, simply by incrementally increasing tensile plastic deformation in the martensite phase. This surprising response is linked to the large positive, +51.33 × 10−6 K−1, and negative, −34.51 × 10−6 K−1, CTE anisotropy, at the lattice level, along the different crystal directions in martensite. Similar CTE anisotropy is also shown experimentally in CoNiGa and TiNb alloys. In a model TiNb alloy, giant macroscopic CTEs of +181 × 10−6 K−1 and −142 × 10−6 K−1 are measured. A connection between the CTE anisotropy and the martensitic transformation in these and other materials systems such as NiTi, pure uranium, and PbTiO3 is later made. It is shown that negative or positive thermal expansion crystallographic directions are connected to the crystallographic relationship between the austenite and martensite lattices, and can easily be predicted using the lattice parameters of austenite and martensite phases. Our current observations and analyses suggest that the tunability of the macroscopic CTE through thermo-mechanical processing is universal in materials––both ceramic and metals––that undergo martensitic transformations.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Thermal Expansion and Ionic Conductivity · Ferroelectric and Piezoelectric Materials · Thermodynamic and Structural Properties of Metals and Alloys
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (22)
Show source-provided references
1. Negative thermal expansion materials: technological key for control of thermal expansion10.1088/1468-6996/13/1/013001 ↗
2. The origin of the ‘Invar’ effect10.1088/0370-1328/82/2/314 ↗
3. The Invar problem10.1016/0304-8853(91)90828-X ↗
4. First-principles calculations of the instability leading to the Invar effect10.1103/PhysRevB.47.8706 ↗
5. Temperature-induced valence transition and associated lattice collapse in samarium fulleride10.1038/nature01994 ↗
6. Negative thermal expansion in ZrW2O8 and HfW2O810.1021/cm9602959 ↗
7. Negative thermal expansion from 0.3 to 1050 Kelvin in ZrW2O810.1126/science.272.5258.90 ↗
8. Thermal contraction10.1038/40052 ↗
9. Thermal contraction10.1016/0160-9327(95)93586-4 ↗
10. Compounds that contract on heating10.1021/ic980253h ↗
11. Thermal expansion of carbon structures10.1103/PhysRevB.68.035425 ↗
12. Thermal-expansion anisotropy and acosutic-emission of NaZr2P3O12 family ceramics10.1111/j.1151-2916.1991.tb06888.x ↗
13. Measurement of the lattice plane strain and phase fraction evolution during heating and cooling in shape memory NiTi10.1063/1.3245308 ↗
14. Thermal expansion of alpha uranium10.1016/0022-3115(66)90095-X ↗
15. SMARTS – a spectrometer for strain measurement in engineering materials10.1007/s003390201747 ↗
16. B. Clausen, Los Alamos National Laboratory, LA-UR 04–6581, 2004, Los Alamos, NM.
17. Rietveld refinement with spallation neutron powder diffraction data10.1107/S0021889882012722 ↗
18. Thermal-expansion coefficients for monoclinic crystals – phenomenological approach
19. The effect of electronic and magnetic valences on the martensitic transformation of CoNiGa shape memory alloys10.1016/j.actamat.2012.02.044 ↗
20. Martensitic transformation, shape memory effect and superelasticity of Ti-Nb binary alloys10.1016/j.actamat.2006.01.019 ↗
21. Determining recoverable and irrecoverable contributions to accumulated strain in a NiTiPd high-temperature shape memory alloy during thermomechanical cycling10.1016/j.scriptamat.2011.03.019 ↗
22. Strain glass transition in a multifunctional β-type Ti alloy