Influence of selected alloying variations on liquid metal embrittlement susceptibility of quenched and partitioned steels

In this work, the influence of selected alloying variations on Zn-assisted liquid metal embrittlement (LME) susceptibility of Zn-coated advanced high strength steels (AHSS) is investigated. Cold-rolled AHSS alloys of different carbon (C), manganese (Mn), silicon (Si), and aluminum (Al) concentrations were continuous-annealed to generate a third generation AHSS microstructure (composed of martensite and retained austenite) via quenching and partitioning. High temperature tension tests using simulated spot-weld thermomechanical cycles revealed no significant influence of C and Mn variations on the Zn-LME susceptibility of AHSS. On the other hand, Zn-LME susceptibility was strongly correlated with the Si content of AHSS. A direct comparison of the (reacted) coating microstructures of the Si-alloyed and Low-Si AHSS variants revealed that Si in the AHSS substrate suppresses Fe-Zn alloying reactions and retards the nucleation and growth of Fe-Zn intermetallic phases at the coating-substrate interface in these spot weld simulations. The suppressed intermetallic formation at elevated Si concentrations is consistent with phase equilibria considerations in the Fe-Zn-Si ternary system. In the context of Zn-assisted LME, therefore, Si is hypothesized to aggravate LME behavior by increasing the liquid Zn availability for embrittlement and promoting direct contact between liquid Zn and the AHSS steel substrate. (c) 2022 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http:// creativecommons.org/licenses/by-nc-nd/4.0/).

Automated summary

This work investigates the influence of selected alloying variations on Zn-assisted liquid metal embrittlement (LME) susceptibility of Zn-coated advanced high strength steels (AHSS). The study reveals that the Si content of AHSS is strongly correlated with Zn-LME susceptibility, and Si suppresses the formation of Fe-Zn intermetallic phases at the coating-substrate interface.