Microstructural evolution, electrochemical and corrosion properties of Al x CoCrFeNiTi y high entropy alloys
- 1. Department of Materials Science and Engineering, Monash University, Clayton, Victoria 3800 (Australia)
- 2. Institute for Frontier Materials, Deakin University, VIC 3216 (Australia)
- 3. Centre for Materials and Surface Science, Department of Chemistry and Physics, La Trobe University, Melbourne, Victoria 3086 (Australia)
- 4. Department of Materials Science and Engineering, The Ohio State University, Columbus, OH 43210 (United States)
- 5. College of Engineering and Computer Science, Australian National University, ACT 2601 (Australia)
Description
Highlights: • The microstructural evolution of AlxCoCrFeNiTiy CCAs is investigated in details using XRD, SEM and TEM. • Good corrosion resistance of these CCAs in 0.6 M NaCl is revealed, with fine pitting as the main type of corrosion. • The composition of the surface films was elaborated by XPS which provided new insights on the corrosion mechanisms of CCAs. -- Abstract: The microstructure of the AlxCoCrFeNiTiy high entropy alloy (HEA) system was studied using X-ray diffraction, scanning and transmission electron microscopy. A microstructural evolution from single-phase FCC to FCC + BCC + B2 occurred with increasing Al content. The addition of a comparatively small amount of Ti led to the formation of a Fe-Cr sigma phase. The corrosion characteristics of the alloy system were studied across different compositions, with such an alloy system exhibiting a high resistance to general corrosion, superior to stainless steel 304L in 0.6 M NaCl. Cyclic potentiodynamic polarisation suggested that the HEAs studied underwent pitting corrosion following breakdown. From exposure testing, it was seen that very fine pitting, although not extensive in nature, was the principle form of corrosion for AlxCoCrFeNiTiy after prolonged immersion. There was little evidence of microgalvanic corrosion or selective dissolution of a particular phase observed, despite the heterogeneous microstructure and significant elemental segregation in the alloys studied. The composition of the surface films formed upon the AlxCoCrFeNiTiy alloys were elaborated by X-ray photoelectron spectroscopy, which provided new and further insights regarding the surface films of such alloys. The study herein contributes to an emerging understanding of the corrosion characteristics of high entropy alloys.
Additional details
Identifiers
- DOI
- 10.1016/j.matdes.2019.107698;
- PII
- S0264127519301352;
Publishing Information
- Journal Title
- Materials and Design
- Journal Volume
- 170
- Journal Page Range
- vp.
- ISSN
- 0264-1275
- CODEN
- MADSD2
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55050378
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALLOY SYSTEMS; BCC LATTICES; CORROSION RESISTANCE; DISSOLUTION; ELECTROCHEMISTRY; ENTROPY; FCC LATTICES; FILMS; MICROSTRUCTURE; PITTING CORROSION; POLARIZATION; SCANNING ELECTRON MICROSCOPY; SODIUM CHLORIDES; STAINLESS STEEL-304L; SURFACES; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ALLOYS; AUSTENITIC STEELS; CARBON ADDITIONS; CHEMICAL REACTIONS; CHEMISTRY; CHLORIDES; CHLORINE COMPOUNDS; CHROMIUM ALLOYS; CHROMIUM-NICKEL STEELS; COHERENT SCATTERING; CORROSION; CORROSION RESISTANT ALLOYS; CRYSTAL LATTICES; CRYSTAL STRUCTURE; CUBIC LATTICES; DIFFRACTION; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; HALIDES; HALOGEN COMPOUNDS; HEAT RESISTANT MATERIALS; HEAT RESISTING ALLOYS; HIGH ALLOY STEELS; IRON ALLOYS; IRON BASE ALLOYS; LOW CARBON-HIGH ALLOY STEELS; MATERIALS; MICROSCOPY; NICKEL ALLOYS; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; SCATTERING; SODIUM COMPOUNDS; SODIUM HALIDES; SPECTROSCOPY; STAINLESS STEELS; STEEL-CR19NI10-L; STEELS; THERMODYNAMIC PROPERTIES; THREE-DIMENSIONAL LATTICES; TRANSITION ELEMENT ALLOYS
Optional Information
- Copyright
- Copyright (c) 2019 The Authors. Published by Elsevier Ltd.