New press-hardening steels (PHSs) have been developed
recently to further improve strength and ductility, meeting the demand of the
automobile industries. PHSs are usually formed by retaining austenite grains
with sufficient fraction and stability for enhancing the
transformation-induced-plasticity (TRIP) effect by deliberately introducing
spherical carbide particles, where austenite grains can be nucleated and grow
in company with their gradual dissolution. However, lamellar pearlite (LP)
microstructure, rather than spherical pearlite (SP), is commonly formed in
automotive steels during industrial hot rolling. This study investigated the
influence of the initial microstructure (LP or SP) on the resultant
microstructures and tensile properties of a new PHS
(Fe-0.29C-1.75Si-1.2Mn-2.1Cr-0.027Nb) after press-hardening with a short
solution period at 915°C and baking at 170°C. The results show that compared to
an initial SP structure, an initial LP structure resulted in higher yield
strength (YS), ultimate tensile strength (UTS), and total elongation (TE) after
the press-hardening at 915°C for 20-30 s. On increasing the
solution period to 25 s, the YS, UTS, and TE of the LP specimen were higher
than those of the SP specimen (by approximately 35 MPa, 75 MPa, and 1%,
respectively) and
the 22MnB5 specimen (by 440 MPa,
490 MPa, and 3%, respectively). The austenitic reversion kinetics in the
solution were simulated using DICTRA. The simulation results indicate that
lamellar cementite dissolves more rapidly than the spherical one under
identical solution treatments. Moreover, the austenite that nucleated and grew
on the lamellar cementite had a higher C content than the austenite on the
spherical cementite. Thus, compared to an initial SP structure, an initial LP
structure resulted in a lower start temperature of martensite transformation (
Ms)
under identical press-hardening processes. This resulted in a higher
dislocation density in martensite in the LP specimen, improving its YS and
retaining more austenite, thereby enhancing the TRIP effect after
press-hardening and improving work hardening. Thus, compared to an initial SP
structure, the LP one resulted in higher resultant YS, UTS, and TE after press-hardening
with a solution period of 20-30 s.