3.1. Crystal Growth of P-Rich C2S in the Modified Slag
Figure 1 shows the SEM images of the modified slag with different holding times at 1673 K, and the EDS results are listed in
Table 2. From the figure, gray C
2S, black RO (FeO-MgO-MnO solid solution), and light gray matrix phases were observed, and the EDS analysis indicated that no phosphorus was found in RO and matrix phases, which means all phosphorus was enriched in C
2S. As can be seen in
Figure 1a,b, many small C
2S grains can be observed. After holding at 1673 K for 40 min, the small grains gradually disappeared, as shown in
Figure 1c. Meanwhile, the growth of the remaining C
2S grains was obvious, and the number of C
2S grains per unit area decreased significantly. With the increase in holding time, it was found that adjacent C
2S grains were connected with each other and eventually formed larger grains, shown in
Figure 1d–f.
Figure 2 shows a frequency histogram of the grain size distribution for C
2S with different holding times at 1673 K. Generally, a grain size above 30 μm was favorable for the liberation of C
2S, while below 30 μm it was difficult to liberate. At the beginning (5 min), almost all C
2S grains were below 30 μm. After 40 min, half of the grains were larger than 30 μm. The grains above 30 μm reached 90% when the holding time reached 240 min. At 360 min, the situation was similar to that of 240 min, except that 60–110 μm grains were more numerous than those at 240 min. Considering the energy consumption, 240 min was the optimum holding time.
Note that the ratios of Mg to Fe in the RO phase with different holding times were all greater than 6 (Mg/Fe > 6), which is obviously high. According to Engstrom et al. [
26], MgO precipitates earlier in the slag during cooling due to the higher melting point, and FeO and MnO have the same chance to dissolve into MgO, but FeO precipitates earlier than MnO. Thus, it can be concluded that MnO did not precipitate before quenching in this work.
Table 3 shows the content of phosphorus in C
2S with different holding times at 1673 K. It can be seen that, considering reasonable error, the phosphorus content increased with holding time, and it was nearly three times higher than that in the original slag (2.23%).
3.2. Stratification of P-Rich C2S in the Modified Slag
Due to lower specific gravity, C
2S would float through the molten slag and lead to stratification [
10]. In
Section 3.1, no obvious stratification was found, owing to the wall effect. To investigate the stratification of P-rich C
2S, kilo-scale modification of the slag was carried out at 1673 K for 240 min.
Figure 3 shows the XRD patterns of the upper and lower modified slags on a kilo-scale. It can be seen from the figure that C
2S, RO, and the spinel were the main phases in the upper slag. Besides these, a few weak calcium ferrite (C
2F) peaks can be observed. According to thermodynamic prediction calculations correlated with experimental results by Gautier et al. [
27], C
2F crystallizes at 1333 K in BOF slag. Thus, due to the high quenching temperature (1673 K) in this work, the thermodynamic conditions for crystallization were not sufficient for C
2F. For the lower slag, C
2S and the spinel were the main phases. Note that the intensity of C
2S in the upper was higher than that in the lower, and the relative intensity of C
2S and spinel in the upper was obviously higher than that of the lower, which indicates a preferential growth of C
2S over other phases in the upper.
Figure 4 shows the SEM images of the upper and lower modified slags on the kilo-scale, and the EDS results are listed in
Table 4. For the upper, C
2S was spherical with a grain size in the range of 20–110 μm, and several holes can be observed (
Figure 4a). Due to volume expansion caused by crystal transformation of C
2S during cooling, microcracks occurred on C
2S, which can be seen clearly in
Figure 4b. The RO phase was about 20–40 μm, and spinel was dispersed in the matrix, forming a strip shape with a smaller size. These phases in the upper slag were independent of each other, and the interface between each phase was clear, which was favorable for the liberation of C
2S. For the lower slag, the micromorphology of the slag was obviously different from that of the upper. C
2S particles in the lower slag were much smaller (less than 3 μm) than those in the upper slag, and these small grains were arranged in a flower pattern, as shown in
Figure 4c. Note that C
2S was embedded in spinel, which can be seen clearly in
Figure 4d, and it was not conducive to the liberation of C
2S.
From
Table 4, it can be seen that 9.81 at% Fe dissolved in C
2S for the lower slag. In the early holding stage, C
2S precipitated first and grew quickly. At this stage, C
2S mainly grew by itself, controlled by mass transfer, and the viscosity of the slag was relatively lower, which was conducive to the diffusion of ions and the floating of C
2S. C
2S floated above the molten slag, and this led to the decrease of Ca and Si in the lower part of molten slag. Thus, in the middle holding stage, C
2S precipitated with more Fe, Mg, etc., in the lower slag and grew slowly, owing to the reduction of Ca and Si. This is consistent with the XRD results in
Figure 3. In the late holding stage, the growth of C
2S in the upper was mainly due to the merging of grains, according to
Figure 1d,e. Due to dissolving of Fe, Mg, etc., the specific gravity of C
2S in the lower was relatively higher, which prevented floating, and they were mostly embedded in spinel. Moreover, the increased viscosity of the molten slag was another reason for preventing floating.
Table 5 shows the content of phosphorus in the upper and lower C
2S, which was calculated from the atomic ratios in
Table 4. It can be seen that the content of phosphorus in upper C
2S (6.60%) was about two times higher than that in lower C
2S (3.80%).
3.3. Liberation Degree of P-Rich C2S in the Modified Slag
The above studies proved that the micromorphology of the upper modified slag was conducive to the liberation of C
2S, while that of the lower slag was not. Then, the upper and lower slags were ground. The particle size distribution with different grinding times is shown in
Figure 5. From
Figure 5a, it can be seen that the average particle size of the upper slag was 10.92 μm after grinding for 30 s and 8.12 μm after 180 s. When the grinding time reached 300 s, the average particle size was 7.84 μm, and the size distribution curve almost coincided with that of 180 s, which indicates that prolonging the grinding time after 180 s had no obvious effect on the particle size. The particle size distribution of the lower slag after grinding for 300 s is shown in
Figure 5b. As can be seen in the figure, the average particle size was 8.22 μm, which was larger than that of the upper slag. This indicates that the lower slag was more difficult to grind than the upper, which may be due to more Fe-bearing phases.
Figure 6. SEM images of the upper modified slag after different grinding times. It can be seen from
Figure 6 that C
2S existed both as free particles and locked particles, most of which existed in the form of free particles. According to the classification of locked particles, the C
2S locked particles in the upper slag belonged to the adjacent type. Here, the spinel and the matrix are collectively referred to as the M phase, and for the RO phase, they locked with the M phase. SEM images of the lower slag after grinding for 300 s are shown in
Figure 7. It can be seen that most of C
2S existed in the form of locked particles with the M phase, and they are mostly of the encapsulated type.
After respectively grinding the upper and lower slags, the liberation degree of C
2S was determined by SEM. The liberation degree of a mineral (
L) is defined by Equation (1):
in which
qf is content of free particles, and
ql is content of locked particles. In this work, the particle counting method was used to calculate the liberation degree of C
2S, and the calculation Equation is as follows:
in which
Nf is the number of C
2S free particles, and
Nl is the number of C
2S locked particles. The liberation degree of C
2S in the upper and lower modified slags as calculated by Equation (2) is listed in
Table 6. As can be seen in the table, the liberation degree of C
2S in the upper slag increased with grinding time of the modified slag, from 86.02% to 95.92% in the range of 30–300 s. For the lower slag ground for 300 s, the liberation degree of C
2S was only 40.07%. Therefore, considering energy consumption, 180 s was the optimum grinding time for liberation of C
2S from the upper slag.