4.5 Article

Effect of Variation of Martensite with a Constant Carbon Content on Mechanical Behavior and Sliding Wear of Dual Phase Steels

Journal

TRIBOLOGY LETTERS
Volume 70, Issue 3, Pages -

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11249-022-01616-0

Keywords

Dual phase steels; Wear resistance; Mechanical properties; Strain-hardening rate; Archard law

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This study investigates the effect of martensite content on the tribological properties of dual phase steel by maintaining a constant carbon content. Increasing normal load results in a decrease in specific wear rate, due to the high work-hardening capacity and the formation of a more durable tribofilm. However, a further increase in normal load leads to an increase in specific wear rate and a reduction of oxide coverage. Worn debris consists mainly of metallic particles during the running-in stage and Fe3O4 oxide during the steady-state stage.
In a dual phase steel, an increase in the martensite volume fraction leads to a decrease in its carbon content, and hence, elucidating the effect of martensite content on the mechanical and tribological behaviors has not been possible. For the first time, the present work dealt with this subject by maintaining a constant amount of carbon in different volume fractions of martensite. Tribological properties was evaluated via a pin-on-disk sliding tribometer. The study of wear tracks and debris revealed oxidative wear as the dominant wear mechanism. Increasing normal load from 10 to 30 N resulted in a decrease in the specific wear rate, which was related to the high work-hardening capacity. This resulted in higher surface hardness, accommodating the formation of a more durable tribofilm on the surface, and a lower coefficient of friction. However, the increase in normal load from 30 to 60 N resulted in an increase in the specific wear rate and reduction of oxide coverage on the sliding surface due to high surface stresses. The worn debris were mainly identified as metallic in the running-in stage and Fe3O4 oxide in the steady-state stage. [GRAPHICS] .

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