Method for preparing blast furnace blow-in coal

Abstract

On the basis of data obtained by means of analyzing coal, a first and second coal type satisfying conditions are selected, the ash melting point of the mixed coal resulting from mixing the first and second coal types is derived on the basis of a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3, on the basis of the ash melting point of the mixed coal and the four-dimensional state diagram, an additive causing the ash melting point of the mixed coal to be at least 1400 C. at the lowest quantity when added to the mixed coal is selected from SiO.sub.2, MgO, and CaO, the addition quantity of the additive is derived, the first coal type and second coal type are mixed to result in the mixed coal, and the addition quantity of the additive is added to the mixed coal.

Claims

1. A method for preparing blast furnace blow-in coal blown from a tuyere into an interior of a blast furnace main body of a blast furnace installation, the method comprising: a first step of analyzing a moisture content of run-of-mine coal, ash of the coal, and weight percentages of Al, Si, Ca and Mg in the ash; a second step of selecting, on the basis of data obtained by analysis, a first coal type, of which the moisture content in the run-of-mine coal is less than 15% by weight, and a total weight of Al, Si, Ca and Mg oxides in the ash is not less than 70% by weight of the ash weight, and, when the total of Al, Si, Ca and Mg oxides in the ash is taken as 100% by weight, an Al.sub.2O.sub.3 content is 20% by weight 5% by weight, and an SiO.sub.2 content is not less than 70% by weight; a third step of selecting, on the basis of data obtained by analysis, a second coal type, of which the moisture content in the run-of-mine coal is not less than 15% by weight, and the total weight of Al, Si, Ca and Mg oxides in the ash is not less than 70% by weight of the ash weight, and, when the total of Al, Si, Ca and Mg oxides in the ash is taken as 100% by weight, the Al.sub.2O.sub.3 content is 20% by weight 5% by weight, and the SiO.sub.2 content is not less than 35% by weight and not greater than 45% by weight, and an MgO content is not less than 0% by weight and not greater than 25% by weight; a fourth step of deriving an ash melting point of a mixed coal upon mixing the selected first coal type and the second coal type, on the basis of a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total weight of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% by weight and the Al.sub.2O.sub.3 content is converted to 20% by weight; a fifth step of selecting SiO.sub.2, MgO or CaO as an additive to cause the ash melting point of the mixed coal upon mixing the selected first coal type and the second coal type to be not less than 1400 C. when added to the mixed coal in the smallest quantity, on the basis of the ash melting point of the mixed coal and the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3; a sixth step of deriving an addition quantity of the selected additive to the mixed coal; a seventh step of mixing the selected first coal type and the second coal type to result in mixed coal; and an eighth step of adding the additive in the addition quantity to the mixed coal.

2. The method for preparing blast furnace blow-in coal according to claim 1, wherein, in the fifth step, the CaO is selected as the additive upon the ash melting point of the mixed coal being within a region not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% by weight and the Al.sub.2O.sub.3 content is converted to 20% by weight, and being below a first boundary line according to equation (1) representing a relationship between a content x of the SiO.sub.2 and a content y of the CaO; the SiO.sub.2 is selected as the additive upon the ash melting point of the mixed coal being within a region not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3, and being above a second boundary line according to equation (2) representing a relationship between the SiO.sub.2 content x and the CaO content y; and the MgO is selected as the additive upon the ash melting point of the mixed coal being within a region not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3, and being above the first boundary line and below the second boundary line:
y=0.083x.sup.26.67x+166.3(1)
y=0.065x.sup.26.86x+177.4(2).

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a flowchart illustrating a procedure of a method for preparing blast furnace blow-in coal pertaining to a first embodiment of the present invention.

(2) FIG. 2 is a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 for the ash of the blast furnace blow-in coal pertaining to the first embodiment of the present invention.

(3) FIG. 3 is a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 for the ash of the blast furnace blow-in coal pertaining to a second embodiment of the present invention.

(4) FIG. 4 is a diagram used for deriving a first boundary line in FIG. 3.

(5) FIG. 5 is a diagram used for deriving a second boundary line in FIG. 3.

(6) FIG. 6 is a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 used for describing a confirmation test of the method for preparing blast furnace blow-in coal pertaining to the embodiments of the present invention.

DESCRIPTION OF EMBODIMENTS

(7) Embodiments of the method for preparing blast furnace blow-in coal pertaining to the present invention will be described based on the drawings, but the present invention is not limited only to the following embodiments described based on the drawings.

First Embodiment

(8) A first embodiment of the method for preparing blast furnace blow-in coal pertaining to the present invention will be described based on FIGS. 1 and 2.

(9) The blast furnace blow-in coal pertaining to this embodiment is blast furnace blow-in coal blown from a tuyere into the interior of a blast furnace main body of a blast furnace installation, which, as illustrated in FIG. 1, can be easily prepared by analyzing the moisture content of run-of-mine coal, the ash of the coal, and the weight percentages of Al, Si, Ca and Mg in the ash of the coal (first step S1); selecting a first coal type satisfying conditions A (second step S2); selecting a second coal type with a low ash melting point satisfying conditions B different from conditions A (third step S3); deriving the ash melting point of the mixed coal obtained by mixing these coals (first coal type and second coal type) (fourth step S4); selecting an additive on the basis of the ash melting point of the mixed coal and a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 (fifth step S5); deriving an addition quantity of the selected additive (sixth step S6); mixing the selected first coal type and the second coal type to result in mixed coal (seventh step S7); and adding the additive in the addition quantity to the mixed coal (eighth step S8).

(10) In the first step S1, the moisture content of run-of-mine coal and the composition of the ash of the coal are the data most basically used as the quality of coal (run-of-mine coal), and are obtained by, for example, the industrial analysis set forth in JIS M 8812 (2004) implemented when the run-of-mine coal is produced or used.

(11) In the first step S1, the weight percentages of Al, Si, Ma and Ca in the ash of the coal are the data most basically used as the quality of coal (run-of-mine coal), and are obtained by, for example, the analysis method of metal in exhaust gas set forth in JIS K 0083 (method by ICP (high-frequency inductively coupled plasma)) or the analysis method of coal ash and coke ash set forth in JIS M 8815 implemented when the run-of-mine coal is produced or used.

(12) Conditions A in the second step S2 are that the moisture content of the run-of-mine coal is less than 15% by weight, and the total weight of Al, Si, Ca and Mg oxides in the ash is not less than 70% by weight of the ash weight, and, as illustrated in FIG. 2, when the total of Al, Si, Ca and Mg oxides in the ash is taken as 100% by weight, the Al.sub.2O.sub.3 content is 20% by weight5% by weight, and the SiO.sub.2 content is not less than 70% by weight.

(13) Conditions B in the third step S3 are that the moisture content of the run-of-mine coal is not less than 15% by weight, and the total weight of Al, Si, Ca and Mg oxides in the ash is not less than 70% by weight of the ash weight, and, as illustrated in FIG. 2, when the total of Al, Si, Ca and Mg oxides in the ash is taken as 100% by weight, the Al.sub.2O.sub.3 content is 20% by weight5% by weight, and the SiO.sub.2 content is not less than 35% by weight and not greater than 45% by weight, and the MgO content is not less than 0% by weight and not greater than 25% by weight.

(14) Examples of run-of-mine coal of the second coal type satisfying conditions B are generally low-grade coals (oxygen atom content (dry base): more than 18% by weight; average pore diameter: from 3 to 4 nm) having a low ash melting point (for example, 1200 C.), such as lignite, sub-bituminous coal, bituminous coal and the like. Other coals that may be used include dry-distilled coals, specifically those having an oxygen atom content (dry base) of from 10 to 18% by weight, which has been greatly reduced by desorption of tar-producing groups such as oxygen-containing functional groups (carboxyl groups, aldehyde groups, ester groups, hydroxyl groups and the like), specifically those in which decomposition (reduction) of the main skeleton (combustion components of mainly C, H, O) has been greatly suppressed, and having an average pore diameter of from 10 to 50 nm by means of removing moisture by heating (from 110 to 200 C. for from 0.5 to 1 hour) low-grade coal in a low-oxygen atmosphere (oxygen concentration: not greater than 5% by volume) to dry it, and then removing water, carbon dioxide, tar and the like as dry-distilled gas or dry-distilled oil by dry distillation while heating (from 460 to 590 C. (preferably from 500 to 550 C.) for from 0.5 to 1 hour) in a low-oxygen atmosphere (oxygen concentration: not greater than 2% by volume), and then cooling (not higher than 50 C.) in a low-oxygen atmosphere (oxygen concentration: not greater than 2% by volume).

(15) In the fourth step S4, the weight ratio of SiO.sub.2, CaO and MgO in the ash of the mixed coal is determined on the basis of the ash composition data of the first coal type obtained in the first step S1, the ash composition data of the second coal type obtained in the first step S1, and the mixing proportion of the first coal type and the second coal type, by taking the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal as 100% by weight and converting the Al.sub.2O.sub.3 content in the ash of the mixed coal to 20% by weight. On the basis of the weight ratio of SiO.sub.2, CaO and MgO in the ash of the mixed coal and a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 2, the ash melting point of the mixed coal is derived. The mixing proportion of the first coal type and the second coal type may be set as appropriate; for example, it is advantageous when the second coal type is not less than 25% by weight.

(16) In the fifth step S5, on the basis of the ash melting point of the mixed coal derived in the fourth step S4 and the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 2, one type of SiO.sub.2, MgO or CaO is selected as an additive to cause the ash melting point of the mixed coal to be not less than 1400 C., which is higher than the hot air (1200 C.) blown into the interior from the tuyere on the bottom side on the side of the blast furnace main body of the blast furnace installation, when added to the mixed coal in the smallest quantity (addition quantity). Examples of SiO.sub.2 sources include silica stone, clay and the like. Examples of MgO sources include MgO powder, natural minerals, dolomite, magnesium carbonate and the like. Examples of CaO sources include quicklime, limestone, serpentinite and the like.

(17) In the sixth step S6, the addition quantity of the additive to the mixed coal is derived on the basis of the ash melting point of the mixed coal derived in the fourth step S4, the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 2, and the additive selected in the fifth step S5.

(18) In the eighth step S8, blast furnace blow-in coal is prepared by adding the additive selected in the fifth step S5 to the mixed coal in the addition quantity derived in the sixth step S6.

(19) Because the blast furnace blow-in coal produced by the method for preparing blast furnace blow-in coal pertaining to this embodiment is a mixed coal of the first coal type satisfying conditions A and the second coal type satisfying conditions B, and because the additive selected on the basis of the ash melting point of the mixed coal and a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 has been added in the addition quantity to the mixed coal, the ash melting point of the blast furnace blow-in coal is from 100 to 150 C. higher than the temperature of the hot air blown into the interior from the tuyere of the blast furnace main body, and the ash of blast furnace blow-in coal (blast furnace blow-in ash) does not melt by the hot air and as a result, it can suppress accretion of blast furnace blow-in ash or blockage by the blast furnace blow-in ash in the pathway leading to the tuyere of the blast furnace main body.

(20) For this reason, with the blast furnace blow-in coal pertaining to this embodiment, because the additive is selected from SiO.sub.2, MgO or CaO and the addition quantity of the selected additive is derived, the addition quantity of the additive can be reduced even though the ash melting point of the mixed coal obtained by mixing the first coal type and the second coal type is lowered to less than 1400 C., unlike the case where only calcium oxide can be selected as an additive. As a result, a decrease in the amount of heat generation of the obtained blast furnace blow-in coal can be suppressed.

(21) Therefore, by the method for preparing blast furnace blow-in coal pertaining to this embodiment, it is possible to obtain blast furnace blow-in coal that suppresses accretion of blast furnace blow-in ash or blockage by blast furnace blow-in ash in a pathway leading to a tuyere of a blast furnace main body while suppressing a decrease in the amount of heat generation despite containing low-ash-melting-point coal.

(22) Additionally, because one type of SiO.sub.2, CaO or MgO can be selected as the additive, unlike conventional pulverized coal (blast furnace blow-in coal) obtained by adding calcium oxide as flux together with single pulverized coal or mixed pulverized coal, the ash melting point of the blast furnace blow-in coal obtained by adding the additive to a mixed coal of the first coal type and the second coal type can be increased to not less than 1400 C., despite containing a first coal type of which the SiO.sub.2 content in the ash is not less than 70% by weight and a low-ash-melting-point second coal type of which the SiO.sub.2 content in the ash is not less than 35% by weight and not greater than 45% by weight.

Second Embodiment

(23) A second embodiment of the method for preparing blast furnace blow-in coal pertaining to the present invention will be described based on FIG. 1 and FIGS. 3 to 5.

(24) This embodiment employs a procedure illustrated in FIG. 1 in which the fifth step S5 of the first embodiment has been modified. The other steps are roughly the same as those illustrated in FIG. 1, and duplicate descriptions will be omitted as appropriate.

(25) In this embodiment, in the fifth step S5 of selecting the additive added to the mixed coal, first, it is specified where the ash melting point of the mixed coal derived in the fourth step S4 performed prior to the fifth step S5 is positioned in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the coal is taken as 100% by weight and the Al.sub.2O.sub.3 content is converted to 20% by weight, illustrated in FIG. 3. In short, it is specified where the ash melting point of the mixed coal is positioned in region D encompassed by the solid line in FIG. 3, which is the region in which the ash melting point of coal is not greater than 1400 C. Furthermore, if the ash melting point of the mixed coal is positioned outside region D, the mixed coal can be used as blast furnace blow-in coal without adding the additive to the mixed coal because the ash melting point of that mixed coal is higher than 1400 C.

(26) Next, a first boundary line L1 which results in the smallest addition quantity of the additive is derived by selecting CaO or MgO as the additive on the basis of the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 3.

(27) The first boundary line L1, as illustrated in FIGS. 3 and 4, is a curve that satisfies, for example, equation (1) representing the relationship between SiO.sub.2 content x and CaO content y, which passes through the location where the SiO.sub.2 content is 35% by weight and the CaO content is 35% by weight, and the location where the SiO.sub.2 content is 41% by weight and the CaO content is 33% by weight, and the location where the SiO.sub.2 content is 45% by weight and the CaO content is 35% by weight, when the total of Al, Si, Ca and Mg oxides in the ash of the coal is taken as 100% by weight.
y=0.083x.sup.26.67x+166.3(1)

(28) A second boundary line L2 which results in the smallest addition quantity of the additive is derived by selecting SiO.sub.2 or MgO as the additive on the basis of the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 3.

(29) The second boundary line L2, as illustrated in FIGS. 3 and 5, is a curve that satisfies, for example, equation (2) representing the relationship between SiO.sub.2 content x and CaO content y, which passes through the location where the SiO.sub.2 content is 60% by weight and the CaO content is 0% by weight, and near the location where the SiO.sub.2 content is 63% by weight and the CaO content is 3% by weight, and near the location where the SiO.sub.2 content is 65% by weight and the CaO content is 7% by weight, and near the location where the SiO.sub.2 content is 67% by weight and the CaO content is 9% by weight, and near the location where the SiO.sub.2 content is 68% by weight and the CaO content is 12% by weight, when the total of Al, Si, Ca and Mg oxides in the ash of the coal is taken as 100% by weight.
y=0.065x.sup.26.86x+177.4(2)

(30) In short, in the fifth step S5, the CaO is selected as the additive upon the ash melting point of the mixed coal being within region D, which is not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% and the Al.sub.2O.sub.3 content is converted to 20% by weight, illustrated in FIG. 3, and being below the first boundary line L1 according to equation (1). As a result, it is possible to cause the ash melting point of the blast furnace blow-in coal obtained by adding CaO as the additive to the mixed coal to be not less than 1400 C., despite the CaO addition quantity being lower than in cases where another additive such as Si.sub.2O or MgO is added.

(31) In the fifth step S5, the SiO.sub.2 is selected as the additive upon the ash melting point of the mixed coal being within region D, which is not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% and the Al.sub.2O.sub.3 content is converted to 20% by weight, illustrated in FIG. 3, and being above a second boundary line L2 according to equation (2). As a result, it is possible to cause the ash melting point of the blast furnace blow-in coal obtained by adding SiO.sub.2 as the additive to the mixed coal to be not less than 1400 C., despite the SiO.sub.2 addition quantity being lower than in cases where another additive such as CaO or MgO is added.

(32) In the fifth step S5, the MgO is selected as the additive upon the ash melting point of the mixed coal being within region D, which is not greater than 1400 C. in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% and the Al.sub.2O.sub.3 content is converted to 20% by weight, illustrated in FIG. 3, and being above the first boundary line L1 and below the second boundary line L2. As a result, it is possible to cause the ash melting point of the blast furnace blow-in coal obtained by adding MgO as the additive to the mixed coal to be not less than 1400 C., despite the MgO addition quantity being lower than in cases where another additive such as SiO.sub.2 or CaO is added.

(33) Thus, the position of the ash melting point of the mixed coal derived in the fourth step S4 in the four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 illustrated in FIG. 3 is derived, and on the basis of the position of the ash melting point of the mixed coal, the additive can be selected and the addition quantity of the additive can be derived, and as a result, the additive can be more reliably selected and the addition quantity of the additive can be more reliably derived.

(34) Therefore, by the method for preparing blast furnace blow-in coal pertaining to this embodiment, it is possible to obtain blast furnace blow-in coal that suppresses accretion of blast furnace blow-in ash or blockage by blast furnace blow-in ash in a pathway leading to a tuyere of a blast furnace main body while suppressing a decrease in the amount of heat generation despite containing low-ash-melting-point coal, more reliably than in the embodiment described previously.

EXAMPLES

(35) Working examples performed to confirm the operation and effect of the method for preparing blast furnace blow-in coal pertaining to the present invention will be described below, but the present invention is not limited to only the following working examples described based on various data.

(36) First, as illustrated in FIG. 1, the moisture content of run-of-mine coal and the ash of the coal are analyzed, and the weight percentages of Al, Si, Ca and Mg in the ash of the coal are analyzed in advance (first step S1), a first coal type satisfying conditions A is selected (second step S2), and a second coal type satisfying conditions B different from conditions A is selected (third step S3). In this working example, coal type 1 shown in Table 1 below was selected as the first coal type satisfying conditions A, and coal type 2 shown in Table 1 below was selected as the second coal type satisfying conditions B.

(37) TABLE-US-00001 TABLE 1 Coal Coal Units type 1 type 2 Ash SiO.sub.2 wt. % 31.7 70.3 composition Al.sub.2O.sub.3 wt. % 17.2 23.7 TiO.sub.2 wt. % 1.34 1.14 Fe.sub.2O.sub.3 wt. % 5.98 4.47 CaO wt. % 22.9 0.6 MgO wt. % 5.11 0.6 Na.sub.2O wt. % 1.4 0.42 K.sub.2O wt. % 0.42 1.35 SO.sub.3 wt. % 9.36 P.sub.2O.sub.3 wt. % 0.88 Total of SiO.sub.2, Al.sub.2O.sub.3, CaO and wt. % 76.91 95.2 MgO SiO.sub.2 (as converted when SiO.sub.2, wt. % 41.2 73.8 Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) Al.sub.2O.sub.3 (as converted when SiO.sub.2, wt. % 22.4 24.9 Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) CaO (as converted when SiO.sub.2, wt. % 29.8 0.6 Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) MgO (as converted when SiO.sub.2, wt. % 6.6 0.6 Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) SiO.sub.2 (as converted when SiO.sub.2, wt. % 42.47 78.72 CaO and MgO total 80 wt. %) CaO (as converted when SiO.sub.2, wt. % 30.72 0.64 CaO and MgO total 80 wt. %) MgO (as converted when SiO.sub.2, wt. % 6.8 0.64 CaO and MgO total 80 wt. %)

(38) When the total of Al, Si, Ca and Mg oxides in the ash of coal type 1 was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of coal type 1 were the values shown in Table 1 above. Thus, the ash melting point of coal type 1 is positioned at point P1 in FIG. 6, which is a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the coal is taken as 100% by weight and the Al.sub.2O.sub.3 content is converted to 20% by weight.

(39) When the total of Al, Si, Ca and Mg oxides in the ash of coal type 2 was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of coal type 2 were the values shown in Table 1 above. Thus, the ash melting point of coal type 2 is positioned at point P2 in FIG. 6.

(40) Here, when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of the mixed coal obtained by mixing coal type 1 and coal type 2 were the values shown in Table 2 below. Thus, the ash melting point of the mixed coal is positioned at point P3 in FIG. 6. In short, the ash melting point of the mixed coal is positioned within region D, which is not greater than 1400 C.

(41) TABLE-US-00002 TABLE 2 Mixed coal (wt. %) Ash SiO.sub.2 (as converted when SiO.sub.2, Al.sub.2O.sub.3, CaO 57.5 composition and MgO total 100 wt. %) Al.sub.2O.sub.3 (as converted when SiO.sub.2, Al.sub.2O.sub.3, CaO 23.6 and MgO total 100 wt. %) CaO (as converted when SiO.sub.2, Al.sub.2O.sub.3, CaO 15.2 and MgO total 100 wt. %) MgO (as converted when SiO.sub.2, Al.sub.2O.sub.3, CaO 3.6 and MgO total 100 wt. %) Total of SiO.sub.2, Al.sub.2O.sub.3, CaO and MgO 100.0 SiO.sub.2 (as converted when SiO.sub.2, CaO and MgO 60.3 total 80 wt. %) CaO (as converted when SiO.sub.2, CaO and MgO 15.9 total 80 wt. %) MgO (as converted when SiO.sub.2, CaO and MgO 3.8 total 80 wt. %) Total of SiO.sub.2, CaO and MgO 80.0

(42) Blast furnace blow-in coal obtained by selecting SiO.sub.2 as an additive and adding 25% by weight SiO.sub.2 to the above mixed coal even though the ash melting point P3 of the mixed coal is positioned at a location where MgO is to be selected as the additive in the method for preparing blast furnace blow-in coal pertaining to the second embodiment described above, was used as comparative substance 1. When the total of Al, Si, Ca and Mg oxides in the ash of comparative substance 1 was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of comparative substance 1 were the values shown in Table 3 below. Thus, the ash melting point of comparative substance 1 is positioned at point P4 in FIG. 6, and it is clear that the ash melting point P4 of comparative substance 1 is positioned within region D, in which the ash melting point of coal is not greater than 1400 C.

(43) Blast furnace blow-in coal obtained by selecting CaO as an additive and adding 25% by weight CaO to the above mixed coal was used as comparative substance 2. When the total of Al, Si, Ca and Mg oxides in the ash of comparative substance 2 was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of comparative substance 2 were the values shown in Table 3 below. Thus, the ash melting point of comparative substance 2 is positioned at point P5 in FIG. 6, and it is clear that the ash melting point P5 of comparative substance 2 is positioned within region D, in which the ash melting point of coal is not greater than 1400 C.

(44) Blast furnace blow-in coal obtained by selecting MgO as an additive and adding 25% by weight MgO to the above mixed coal because the ash melting point P3 of the mixed coal is positioned at a location where MgO is to be selected as the additive in the method for preparing blast furnace blow-in coal pertaining to the second embodiment described above, was used as test substance 1. When the total of Al, Si, Ca and Mg oxides in the ash of test substance 1 was taken as 100% by weight and the Al.sub.2O.sub.3 content was converted to 20% by weight, the contents of Si, Ca and Mg oxides in the ash of test substance 1 were the values shown in Table 3 below. Thus, the ash melting point of test substance 1 is positioned at point P6 in FIG. 6, and it is clear that the ash melting point P6 of test substance 1 is positioned in a region in which the ash melting point of coal is not greater than 1400 C.

(45) TABLE-US-00003 TABLE 3 Compar- Compar- Test sub- ative sub- ative sub- stance 1 stance 1 stance 2 Ash SiO.sub.2 (as converted when 46.0 66.0 46.0 compo- SiO.sub.2, Al.sub.2O.sub.3, CaO and sition MgO total 100 wt. %) Al.sub.2O.sub.3 (as converted when 18.9 18.9 18.9 SiO.sub.2, Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) CaO (as converted when 12.2 12.2 32.2 SiO.sub.2, Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) MgO (as converted when 22.9 2.9 2.9 SiO.sub.2, Al.sub.2O.sub.3, CaO and MgO total 100 wt. %) Total of SiO.sub.2, Al.sub.2O.sub.3, 100.0 100.0 100.0 CaO and MgO SiO.sub.2 (as converted when 45.4 65.1 45.4 SiO.sub.2, CaO and MgO total 80 wt. %) CaO (as converted when 12.0 12.0 31.7 SiO.sub.2, CaO and MgO total 80 wt. %) MgO (as converted when 22.6 2.9 2.9 SiO.sub.2, CaO and MgO total 80 wt. %) Total of SiO.sub.2, CaO and 80.0 80.0 80.0 MgO

(46) Thus, it is clear that by this working example, it is possible to obtain blast furnace blow-in coal that suppresses accretion of blast furnace blow-in ash or blockage by blast furnace blow-in ash in a pathway leading to a tuyere of a blast furnace main body while suppressing a decrease in the amount of heat generation despite containing low-ash-melting-point coal, by analyzing the moisture content of run-of-mine coal, the ash of the coal, and the weight percentages of Al, Si, Ca and Mg in the ash of the coal; selecting a first coal type satisfying conditions A; selecting a second coal type satisfying conditions B different from conditions A; deriving the ash melting point of the mixed coal obtained by mixing these coals (first coal type and second coal type) on the basis of a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3 when the total of Al, Si, Ca and Mg oxides in the ash of the mixed coal is taken as 100% by weight and the Al.sub.2O.sub.3 content is converted to 20% by weight; selecting SiO.sub.2, MgO or CaO as an additive to cause the ash melting point of the mixed coal to be not less than 1400 C. when added to the mixed coal in the smallest quantity on the basis of the ash melting point of the mixed coal and a four-dimensional state diagram for SiO.sub.2CaOMgO-20% Al.sub.2O.sub.3; deriving an addition quantity of the additive; mixing the first coal type and the second coal type to result in mixed coal; and adding the additive in the addition quantity to the mixed coal.

(47) Furthermore, a method for preparing blast furnace blow-in coal in which the third step S3 is performed after the second step S2 was described above, but a method for preparing blast furnace blow-in coal in which the second step S2 and the third step S3 are performed simultaneously, or a method for preparing blast furnace blow-in coal in which the second step S2 is performed after the third step S3, may also be used.

INDUSTRIAL APPLICABILITY

(48) The method for preparing blast furnace blow-in coal pertaining to the present invention can be used extremely advantageously in the iron-making industry because it can provide blast furnace blow-in coal that suppresses accretion of blast furnace blow-in ash or blockage by blast furnace blow-in ash in a pathway leading to a tuyere of a blast furnace main body while suppressing a decrease in the amount of heat generation despite containing low-ash-melting-point coal.

REFERENCE SIGNS LIST

(49) A Conditions of first coal type B Conditions of second coal type D Region of ash melting point of mixed coal not greater than 1400 C. L1 First boundary line L2 Second boundary line P1 Ash melting point of coal type 1 P2 Ash melting point of coal type 2 P3 Ash melting point of mixed coal (coal types 1, 2) P4 Ash melting point of comparative substance 1 P5 Ash melting point of comparative substance 2 P6 Ash melting point of test substance 1 S1 First step (analysis step) S2 Second step (first coal type selection step) S3 Third step (second coal type selection step) S4 Fourth step (mixed coal ash melting point derivation step) S5 Fifth step (additive selection step) S6 Sixth step (addition quantity derivation step) S7 Seventh step (mixing step) S8 Eighth step (addition step)