The effects of parametric changes in electropolishing process on surface properties of 316L stainless steel
- 1. Science of Advanced Materials, Central Michigan University, Mt. Pleasant, MI 48859 (United States)
- 2. School of Engineering and Technology, Central Michigan University, Mt. Pleasant, MI 48859 (United States)
- 3. Department of Metallurgy and Materials Engineering, CEET, University of the Punjab, Lahore, 54590 (Pakistan)
- 4. Department of Materials Engineering, University of British Columbia, Vancouver, BC V6T 1Z4 (Canada)
- 5. Department of Mechanical Engineering, The University of Texas Rio Grande Valley, Edinburg, TX 78539 (United States)
Description
Highlights: • 316L stainless steel was electropolished at the oxygen evolution (EPO) and below the oxygen evolution (EPBO) potentials. • EPBO samples displayed low fractional polarity and surface roughness when compared to EPO. • Both electropolished samples (EPO and EPBO) showed higher resistance to corrosion when compared to mechanically polished samples. • EPO and EPBO samples showed enhanced cell proliferation and stellar morphology after 24 h. - Abstract: Corrosion resistance and biocompatibility of 316L stainless steel implants depend on the surface features and the nature of the passive film. The influence of electropolishing on the surface topography, surface free energy and surface chemistry was determined by atomic force microscopy, contact angle meter and X-ray photoelectron spectroscopy, respectively. The electropolishing of 316L stainless steel was conducted at the oxygen evolution potential (EPO) and below the oxygen evolution potential (EPBO). Compared to mechanically polished (MP) and EPO, the EPBO sample depicted lower surface roughness (Ra = 6.07 nm) and smaller surface free energy (44.21 mJ/m2). The relatively lower corrosion rate (0.484 mpy) and smaller passive current density (0.619 μA/cm2) as determined from cyclic polarization scans was found to be related with the presence of OH, Cr(III), Fe(0), Fe(II) and Fe(III) species at the surface. These species assured the existence of relatively uniform passive oxide film over EPBO surface. Moreover, the relatively large charge transfer (Rct) and passive film resistance (Rf) registered by EPBO sample from impedance spectroscopy analysis confirmed its better electrochemical performance. The in vitro response of these polished samples toward MC3T3 pre-osteoblast cell proliferation was determined to be directly related with their surface and electrochemical properties.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.apsusc.2017.03.081Additional details
Identifiers
- DOI
- 10.1016/j.apsusc.2017.03.081;
- PII
- S0169-4332(17)30740-7;
Publishing Information
- Journal Title
- Applied Surface Science
- Journal Volume
- 410
- Journal Page Range
- p. 432-444
- ISSN
- 0169-4332
- CODEN
- ASUSEE
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48078196
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ATOMIC FORCE MICROSCOPY; CELL PROLIFERATION; CORROSION; CORROSION RESISTANCE; CURRENT DENSITY; ELECTROCHEMISTRY; ELECTROPOLISHING; FILMS; FREE ENERGY; IMPEDANCE; IN VITRO; POLARIZATION; ROUGHNESS; STAINLESS STEEL-316L; SURFACES; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALLOYS; AUSTENITIC STEELS; CARBON ADDITIONS; CHEMICAL REACTIONS; CHEMISTRY; CHROMIUM ALLOYS; CHROMIUM STEELS; CHROMIUM-MOLYBDENUM STEELS; CHROMIUM-NICKEL STEELS; CHROMIUM-NICKEL-MOLYBDENUM STEELS; CORROSION RESISTANT ALLOYS; ELECTROLYSIS; ELECTRON SPECTROSCOPY; ENERGY; HEAT RESISTANT MATERIALS; HEAT RESISTING ALLOYS; HIGH ALLOY STEELS; IRON ALLOYS; IRON BASE ALLOYS; LOW CARBON-HIGH ALLOY STEELS; LYSIS; MATERIALS; MICROSCOPY; MOLYBDENUM ALLOYS; NICKEL ALLOYS; PHOTOELECTRON SPECTROSCOPY; PHYSICAL PROPERTIES; POLISHING; SPECTROSCOPY; STAINLESS STEELS; STEEL-CR17NI12MO3-L; STEELS; SURFACE FINISHING; SURFACE PROPERTIES; THERMODYNAMIC PROPERTIES; TRANSITION ELEMENT ALLOYS
Optional Information
- Copyright
- Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.