Dissolved V in austenite of 7%Cr-0.4%V-0.09%N steel (hereinafter, % means mass%) was measured and the solubility product of VN was determined as follows:where T is the absolute temperature in K. The solubility product obtained is 3 to 5 times larger than those in the literature and about one order larger than that for iron. The decrease in the activity coefficient of nitrogen due to the presence of Cr and V in the experimental steel is responsible for the increase in the solubility product of VN.KEY WORDS: precipitation; MX; thermodynamics; activity coefficient.
log([% ][% ])V N 4.38 ϭ Ϫ 8 436 T stituent elements. The detectable limit for V in this study is about 0.42 ppm for the experimental steel. The solubility product of VN is calculated using the following equation assuming that chemical composition of VN is stoichiometric.[%V] [%N] Symbols, [%V] and [%N], denote the dissolved V and N in austenite, and V t , N t denote the total V and N, respectively. Symbol, [%N 0 ], denotes the dissolved N in Fe-V-N alloy which is calculated from the observed values of the dissolved V. The amount of the dissolved vanadium in the matrix, [%V], is assumed to be equal to the amount of the dissolved vanadium observed.
Experimental Results and Discussion
Thermal EquilibriumCharacteristic features of the present analyzing method are that the duration of heat treatment is relatively short, and that the V content of a filtered solution is directly measured. Therefore, firstly, whether the equilibrium in the precipitation of VN is satisfactorily guaranteed by 1 h heating or not becomes a problem. Therefore, the effects of heating rate and heating duration should be discussed. Figure 1 shows the Arrhenius plot of the dissolved V. Open marks correspond to rapid heating where a small coupon was put into a pre-heated furnace and temperature of the coupon was reached to an aiming temperature within 5 min at least. Closed marks correspond to slow heating where a coupon was set in a cold furnace and gradually heated up to an aiming temperature taking 3 h. All coupons were held for 1 h at a temperature in both cases. The figure shows that a linear relationship is found in a wide range of temperature by the rapid heating and the regression line may probably correspond to the equilibrium solubility limit of V in austenite. On the other hand, the amount of the precipitates by the slow heating is insufficient at low temperatures as compared with those of the rapid heating. Figure 2 shows the time dependence of the dissolved V of the rapidly heated specimens at 1 100°C. This figure shows that the enough precipitation has been roughly accomplished by the 1 h rapid heating. Therefore, from Figs. 1 and 2 it is found that the equilibrium of the precipitation of VN in austenite is practically realized by a technique of the rapid heating of a small coupon followed by the short time holding at a temperature. The authors have studied the precipitation behavior of TaC and NbC and concluded that the precipitation of MX in austenite is accomplished wit...