This application claims priority of Taiwanese Patent Application No. 104103462, filed on Feb. 2, 2015, the entire disclosure of which is hereby incorporated by reference.
The disclosure relates to a desulfurization composition, more particularly to a desulfurization composition for desulfurizing molten steel.
During the manufacture of steel in a steel mill, sulfur impurities may be removed via a desulfurization process so as to improve steel quality. Specifically, a desulfurization agent with a low melting point and low viscosity is added to molten steel. The temperature and the partial pressure of oxygen during this desulfurization process are typically set at about 1600° C. and under 20 ppm, respectively.
A conventional method used to increase the desulfurization efficiency of the desulfurization agent and to improve steel quality involves the addition of quicklime (calcium oxide, CaO). As the amount of added quicklime increases, the viscosity of the desulfurization agent may also increase to a point that impedes the desulfurization process. To counter this effect, calcium fluoride (CaF2) may be added to decrease the viscosity of the desulfurization agent. However, calcium fluoride may erode a furnace lining of a furnace used in the manufacture of steel, and the fluorine evaporated during the desulfurization process would greatly harm the human body and environment.
CN 103882183 A discloses a calcium fluoride-free desulfurization refining slag containing 50-60 wt % of calcium oxide, 7-12 wt % of silicon dioxide (SiO2), 28-33 wt % of aluminum oxide (Al2O3) and 4-8 wt % of magnesium oxide (MgO). The weight ratio of calcium oxide to aluminum oxide ranges from about 1.52 to 2.14, preferably from about 1.7 to 1.9. After desulfurization, the melted refining slag mainly contains 12CaO.Al2O3. However, the desulfurization efficiency of the desulfurization refining slag disclosed therein is quite low.
Therefore, the applicants have endeavored to find a calcium fluoride-free desulfurization composition that is associated with improved desulfurization efficiency.
Therefore, a first object of the disclosure is to provide a desulfurization composition that can alleviate at least one of the drawbacks of the prior art.
According to the disclosure, the desulfurization composition includes calcium oxide, silicon dioxide and aluminum oxide. The desulfurization composition is free of an alkali metal oxide. Aluminum oxide is present in an amount ranging from 20 to 26 wt % based on the total weight of the desulfurization composition, and the weight ratio of calcium oxide to aluminum oxide is within a range of 2.19 to 3.
A second object of the disclosure is to provide a method for desulfurizing molten steel comprising mixing the aforesaid desulfurization composition with molten steel.
Other features and advantages of the disclosure will become apparent in the following detailed description of the embodiments with reference to the accompanying drawings, of which:
An embodiment of a desulfurization composition of this disclosure includes calcium oxide, silicon dioxide and aluminum oxide and is free of an alkali metal oxide. Based on the total weight of the desulfurization composition, aluminum oxide is present in an amount ranging from 20 to 26 wt %. The weight ratio of calcium oxide to aluminum oxide is within a range of 2.19 to 3.
In certain embodiments, the weight ratio of calcium oxide to aluminum oxide is within a range of 2.2 to 2.5.
In certain embodiments, aluminum oxide is present in an amount ranging from 24 to 26 wt %.
In certain embodiments, calcium oxide is present in an amount ranging from 57 to 60 wt % based on the total weight of the desulfurization composition. In certain embodiments, calcium oxide is present in an amount ranging from 57 to 59 wt %.
In certain embodiments, silicon dioxide is present in an amount ranging from 7 to 17 wt % based on the total weight of the desulfurization composition. In certain embodiments, silicon dioxide is present in an amount ranging from 10 to 14 wt %.
The desulfurization composition of the disclosure may further include magnesium oxide. Magnesium oxide may be present in an amount ranging from 1 to 10 wt % based on the total weight of the desulfurization composition. In certain embodiments, magnesium oxide is present in an amount ranging from 3 to 7 wt %.
The desulfurization composition of the disclosure may further include other components, including but not limited to dolomite [CaMg(CO3)2] or bauxite (aluminous soil).
The desulfurization composition of this disclosure can be mixed with molten steel under heating (at, e.g., 1600° C.) to perform desulfurization of molten steel. The desulfurization composition after heating includes Ca3SiO5 and 3CaO.Al2O3. Since Ca3SiO5 and 3CaO.Al2O3 have relatively low melting points and similar viscosities to that of CaF2, the desulfurization composition of the disclosure exhibits better desulfurization efficiency for molten steel.
The disclosure will be further described by way of the following examples. However, it should be understood that the following examples are solely intended for the purpose of illustration and should not be construed as limiting the disclosure in practice.
Calcium oxide (Cao, 95% purity), aluminum oxide, silicon dioxide and magnesium oxide powders were mixed to form a desulfurization composition. The amounts of the aforesaid components based on the total weight of the desulfurization composition are listed in Table 1. It should be noted that calcium oxide may be obtained by heating calcium carbonate, and thus calcium oxide having a purity of 95% can be replaced by calcium carbonate having a purity of 98%.
Each of the desulfurization compositions of Comparative Examples 1 to 5 was prepared by mixing components at particular weight percentages as shown in Table 2.
The desulfurization composition of Example 1 was placed in a graphite crucible and was heated to 1600° C. under 1 atm in a frequency furnace to evenly melt the desulfurization composition. The melted desulfurization composition was poured out from the graphite crucible, and was cooled to a temperature below 30° C. so as to obtain a treated desulfurization composition. The treated desulfurization composition was subjected to XRD analysis. The XRD pattern is shown in
The desulfurization compositions of Example 1 and Comparative Example 1 were subjected to differential thermal analysis using Linseis STA PT 1600. The heating and cooling rate was 2° C./min, and the results are shown in
As shown in
The viscosities of the desulfurization compositions of Example 1 and Comparative Example 1 were measured by a viscometer(Brookfield-DV DI RV). The results are shown in
As shown in
Thermo-Calc software, coupled with TCS Steels/Fe-Alloys Database v7.0 and TCS Fe-containing Slag Database v3.2, was used to determine the desulfurization rate of the desulfurization compositions of Example 1 and Comparative Examples 1 to 3. The parameters listed in Table 3 were inputted into the software. The amount of the desulfurization composition was set to be 2 wt % based on the total weight of a mixture containing the desulfurization composition and molten steel.
The graph obtained from the software shows the amounts of C, S, O, Ca, Si, Al and Mg included in the mixture after desulfurization. The amount of sulfur (wt %) at 1600° C. was used to calculate the desulfurization rate. The amount of oxygen (wt %) at 1600° C. was used to calculate a partial pressure (ppm) of oxygen by unit conversion.
The desulfurization rate of the desulfurization composition was calculated according to the following equation:
A=(B−C/B)×100%
It should be noted that the partial pressure of oxygen is an important factor for the desulfurization rate. In the desulfurization process, the lower the partial pressure of oxygen is, the higher the desulfurization rate will be (i.e., the better the desulfurization effect will be).
a) Comparison between Example 1 and Comparative Example 1:
The amounts of sulfur after desulfurization and the desulfurization rates of Example 1 and Comparative Example 1 are listed in Table 4.
As shown in Table 4, the desulfurization rates of Example 1 and Comparative Example 1 are quite close under conditions in which the temperature is 1600° C. and partial pressure of oxygen of the two examples are similar.
The results demonstrate that, without calcium fluoride, the desulfurization composition containing the components with particular
weight percentages still exhibits a high desulfurization rate.
(b) Comparison between Example 1 and Comparative Examples 3 and 4:
The amounts of sulfur after desulfurization and desulfurization rates of the desulfurization compositions of Example 1 and Comparative Examples 3 and 4 are listed in Table 5.
As shown in Comparative Example 3 of Table 5, in which the amount of aluminum oxide was less than 20 wt % and the weight ratio of calcium oxide to aluminum oxide was greater than 3, the desulfurization rate was 58.4 wt % when the partial pressure of oxygen was 2 ppm. The desulfurization rate in Comparative Example 3 was less than the desulfurization rate of Example 1 (83.7 wt %) when the partial pressure of oxygen was 3.77 ppm. Furthermore, in Comparative Example 4 in which the amount of aluminum oxide was greater than 26wt % and the weight ratio of calcium oxide to aluminum oxide was less than 2.19, the desulfurization rate was 81.2 wt % when the partial pressure of oxygen was 2.6 ppm. The desulfurization composition of Example 1 exhibits a better desulfurization rate under a relatively high partial pressure of oxygen (3.77 ppm). It can be predicted that the desulfurization composition of the disclosure would have a higher desulfurization rate than that of Comparative Examples at the same partial pressure of oxygen. The results reveal that the desulfurization rate can be effectively enhanced depending on the particular weight percentages of the components within the desulfurization composition of the disclosure.
It should be noted that the manufacture of steel is conducted at a relatively high temperature (e.g., 1600° C.), and a furnace lining of a high temperature furnace used in the manufacture of steel has to be made of a refractory material. The commonly used lining material is magnesia carbon brick. The following experiment was performed to evaluate the effect of the desulfurization compositions of Example 1 and Comparative Examples 2 and 5 on the erosion rate of the magnesia carbon brick.
Each of the desulfurization compositions of Example 1, Comparative Example 2 and Comparative Example 5 was placed in a graphite crucible, and then heated to 1600° C. in a frequency furnace until melted. A square columnar magnesia carbon brick was then immersed in a respective one of the resultant melted desulfurization compositions for sixty minutes. Before and after immersion, a projected area of an end surface of the magnesia carbon brick on a plane perpendicular to an axis of the columnar magnesia carbon brick was calculated by multiplying a width and a length of the end surface. Erosion rate (%) was calculated according to the following equation:
D=(E−F/E)×100%
The length, width and projected area of the end surface of the magnesia carbon brick before and after immersion as well as the calculated erosion rate are summarized in Table 7. It should be noted that a lower erosion rate indicates that the desulfurization composition causes less erosion to the magnesia carbon brick. The outer appearances of the magnesia carbon bricks after immersion in the melted desulfurization compositions of Example 1, Comparative Example 2 and Comparative Example 5 are respectively shown in
As shown in
To sum up, by adjusting the weight percentage of aluminum oxide and the weight ratio of calcium oxide to aluminum oxide, the desulfurization composition according to this disclosure could obtain a desired melting point and viscosity, and exhibit higher desulfurization efficiency and less erosion rate to the furnace lining.
While the disclosure has been described in connection with what are considered the exemplary embodiments, it is understood that this disclosure is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation so as to encompass all such modifications and equivalent arrangements.
Number | Date | Country | Kind |
---|---|---|---|
104103462 | Feb 2015 | TW | national |