TW202325859A - Method for producing sintered ore - Google Patents
Method for producing sintered ore Download PDFInfo
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- TW202325859A TW202325859A TW111135216A TW111135216A TW202325859A TW 202325859 A TW202325859 A TW 202325859A TW 111135216 A TW111135216 A TW 111135216A TW 111135216 A TW111135216 A TW 111135216A TW 202325859 A TW202325859 A TW 202325859A
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- raw material
- sintering
- sintered ore
- sintered
- ore
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 31
- 238000005245 sintering Methods 0.000 claims abstract description 52
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 51
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims abstract description 47
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000011019 hematite Substances 0.000 claims abstract description 25
- 229910052595 hematite Inorganic materials 0.000 claims abstract description 25
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910052742 iron Inorganic materials 0.000 claims abstract description 23
- 230000004907 flux Effects 0.000 claims abstract description 16
- 239000002994 raw material Substances 0.000 claims description 68
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 26
- 239000000292 calcium oxide Substances 0.000 claims description 13
- 235000012255 calcium oxide Nutrition 0.000 claims description 13
- 230000001678 irradiating effect Effects 0.000 claims description 9
- 239000002893 slag Substances 0.000 claims description 9
- 239000000428 dust Substances 0.000 claims description 8
- 235000019738 Limestone Nutrition 0.000 claims description 5
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 5
- 239000000920 calcium hydroxide Substances 0.000 claims description 5
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 5
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 5
- 239000006028 limestone Substances 0.000 claims description 5
- 239000012256 powdered iron Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 abstract description 28
- 238000000034 method Methods 0.000 abstract description 10
- 239000000843 powder Substances 0.000 abstract description 3
- 239000007858 starting material Substances 0.000 abstract 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- 235000013980 iron oxide Nutrition 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 239000000571 coke Substances 0.000 description 5
- 238000002485 combustion reaction Methods 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052598 goethite Inorganic materials 0.000 description 2
- 238000005469 granulation Methods 0.000 description 2
- 230000003179 granulation Effects 0.000 description 2
- AEIXRCIKZIZYPM-UHFFFAOYSA-M hydroxy(oxo)iron Chemical compound [O][Fe]O AEIXRCIKZIZYPM-UHFFFAOYSA-M 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000008707 rearrangement Effects 0.000 description 2
- 238000009628 steelmaking Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000009770 conventional sintering Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- -1 sintered ore Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/16—Sintering; Agglomerating
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/16—Sintering; Agglomerating
- C22B1/20—Sintering; Agglomerating in sintering machines with movable grates
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/242—Binding; Briquetting ; Granulating with binders
- C22B1/243—Binding; Briquetting ; Granulating with binders inorganic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
本發明是有關於一種使用微波將燒結原料進行加熱而製造燒結礦的方法。The present invention relates to a method for producing sintered ore by using microwaves to heat sintered raw materials.
近年來,以降低環境負荷、特別是削減CO 2排出量為目的,在鋼鐵業中的燒結礦的製造步驟中,不斷推進開發不伴隨焦炭的燃燒的燒結原料的加熱方法。作為不伴隨燃燒的燒結原料的加熱法之一,有照射微波的方法。微波是電磁波的一種,是頻率為300 MHz至300 GHz的範圍的電磁波。已知微波具有對介電體賦予能量而進行加熱的效果,特別是介電常數高的物質容易吸收所照射的微波的能量。 In recent years, for the purpose of reducing the environmental load, especially the reduction of CO 2 emissions, the development of heating methods for sintering raw materials that do not involve the combustion of coke has been promoted in the production process of sintered ore in the iron and steel industry. As one of the heating methods of sintering raw materials without combustion, there is a method of irradiating microwaves. A microwave is a type of electromagnetic wave, and is an electromagnetic wave having a frequency in the range of 300 MHz to 300 GHz. It is known that microwaves have the effect of imparting energy to a dielectric body to heat it, and particularly a substance with a high dielectric constant tends to absorb the energy of irradiated microwaves.
最近,期望使用微波由以赤鐵礦為主成分的鐵礦石來製造燒結礦的技術開發。Recently, the development of technology for producing sintered ore from iron ore mainly composed of hematite using microwaves is expected.
專利文獻1中,以鐵礦石的還原為目的,為了將作為鐵礦石的成分的赤鐵礦及針鐵礦進行加熱,而揭示有照射20 GHz~30 GHz的頻率的微波的方法。揭示有若為高頻(短波長)的20 GHz~30 GHz的微波,則即便是以赤鐵礦或針鐵礦為主成分的鐵礦原料,亦能夠進行加熱或燒結。Patent Document 1 discloses a method of irradiating microwaves at a frequency of 20 GHz to 30 GHz in order to heat hematite and goethite, which are components of iron ore, for the purpose of reduction of iron ore. It is disclosed that even an iron ore raw material mainly composed of hematite or goethite can be heated or sintered if it is a high-frequency (short wavelength) microwave of 20 GHz to 30 GHz.
專利文獻2中,揭示有在利用燃燒反應的已有的燒結機中,自點火爐出來後對表層照射微波,藉此對表層部供給熱,從而提昇燒結礦的品質及回收率的方法。Patent Document 2 discloses a method of improving the quality and recovery rate of sintered ore by irradiating the surface with microwaves after exiting the ignition furnace in a conventional sintering machine utilizing combustion reaction, thereby supplying heat to the surface.
專利文獻3中,揭示有在利用微波照射的燒結礦的製造中,使用未特定氧化鐵的種類的燒結原料,照射2.45 GHz的微波,燒結率與照射時間成正比地上升,在20分鐘內完成燒結。 [現有技術文獻] [專利文獻] Patent Document 3 discloses that in the production of sintered ore by microwave irradiation, using a sintered raw material of an unspecified type of iron oxide and irradiating microwaves of 2.45 GHz, the sintering rate increases in proportion to the irradiation time, and is completed within 20 minutes. sintering. [Prior art literature] [Patent Document]
專利文獻1:日本專利特開2011-184718號公報 專利文獻2:日本專利特表2018-505965號公報 專利文獻3:日本專利特開平07-268494號公報 Patent Document 1: Japanese Patent Laid-Open No. 2011-184718 Patent Document 2: Japanese Patent Application Publication No. 2018-505965 Patent Document 3: Japanese Patent Laid-Open No. 07-268494
[發明所欲解決之課題][Problem to be Solved by the Invention]
但是,專利文獻1中,由於利用20 GHz~30 GHz的高頻的微波進行加熱,故而需要專門的大型迴旋管(gyrotron)裝置,在製程化時設備投資變得過大。However, in Patent Document 1, since heating is performed using high-frequency microwaves of 20 GHz to 30 GHz, a dedicated large-scale gyrotron device is required, and the investment in equipment becomes too large in the process.
專利文獻2中,為了被點火的燒結原料表面的熱補償而使用微波,燒結時的熱能量源是碳的燃燒,因此有產生CO 2的問題。 In Patent Document 2, microwaves are used for thermal compensation of the surface of the ignited sintered raw material, and the heat energy source during sintering is the combustion of carbon, so there is a problem of CO 2 generation.
專利文獻3中,由於以未區別氧化鐵的種類的鐵礦石為燒結原料,故而有利用微波照射的加熱需要長時間的照射而效率低的問題。In Patent Document 3, since iron ore of which iron oxide type is not distinguished is used as a raw material for sintering, there is a problem that heating by microwave irradiation requires long-term irradiation and is inefficient.
如上所述,在燒結步驟中,作為利用焦炭燃燒的加熱的代替,研究了若干使用微波加熱的技術開發。但是,另一方面,現有技術中有如下問題,即,使用以赤鐵礦為主成分的鐵礦石時,需要大規模的微波產生裝置或長時間的微波照射。As described above, in the sintering step, as an alternative to heating by coke combustion, several technical developments using microwave heating have been studied. However, on the other hand, the prior art has a problem that, when using iron ore mainly composed of hematite, a large-scale microwave generator or long-term microwave irradiation is required.
本發明是鑒於所述情況而完成的,本發明的目的在於提供一種燒結礦的製造方法,即便在使用頻率為2.4 GHz~2.5 GHz的微波的情況下,亦以更短時間高效率地將以赤鐵礦為主成分的燒結原料進行加熱而製造燒結礦。 [解決課題之手段] The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a method for producing sintered ore that efficiently converts sintered ore in a shorter time even when microwaves with a frequency of 2.4 GHz to 2.5 GHz are used. Sintered ore is produced by heating a sintered raw material mainly composed of hematite. [Means to solve the problem]
本發明者等人為了解決所述課題而反覆進行了努力研究,結果發現一種燒結礦的製造方法,對在使用以赤鐵礦為主成分的粉狀鐵礦石的情況下,混合有一定量的包含作為介電體的磁鐵礦的原料的燒結原料,藉由照射微波而進行加熱,從而進行燒結。本發明是基於該些見解進一步進行研究而完成的,本發明構成如下。The inventors of the present invention have made intensive studies in order to solve the above-mentioned problems, and as a result, found a method for producing sintered ore in which a certain amount of The sintering raw material including the raw material of magnetite as a dielectric body is sintered by heating by irradiating microwaves. The present invention was completed based on further research based on these findings, and the present invention is constituted as follows.
[1]一種燒結礦的製造方法,其是使燒結原料成塊,所述燒結原料包含以赤鐵礦為主成分的粉狀鐵礦石及助熔劑(flux),所述燒結原料包含以FeO換算為3.0質量%以上的磁鐵礦,且照射微波而將所述燒結原料加熱至1000℃以上。 [2]如[1]所述的燒結礦的製造方法,其中所述燒結原料中混合有包含磁鐵礦的鐵礦石、燒結礦及煉鐵廠內所產生的灰塵的1種以上。 [3]如[1]所述的燒結礦的製造方法,其中所述助熔劑為石灰石、生石灰、熟石灰及煉鐵廠內所產生的礦渣的1種以上。 [4]如[2]所述的燒結礦的製造方法,其中所述助熔劑為石灰石、生石灰、熟石灰及煉鐵廠內所產生的礦渣的1種以上。 [5]如[1]至[4]中任一項所述的燒結礦的製造方法,其中所述微波的頻率為2.4 GHz~2.5 GHz。 [發明的效果] [1] A method for producing sintered ore, comprising agglomerating a sintered raw material comprising powdered iron ore mainly composed of hematite and a flux (flux), the sintered raw material comprising FeO The sintering raw material is heated to 1000° C. or higher by irradiating microwaves to 3.0 mass % or more of magnetite. [2] The method for producing sintered ore according to [1], wherein the sintered raw material is mixed with one or more of iron ore including magnetite, sintered ore, and dust generated in an ironworks. [3] The method for producing sintered ore according to [1], wherein the flux is one or more of limestone, quicklime, slaked lime, and slag generated in ironworks. [4] The method for producing sintered ore according to [2], wherein the flux is one or more of limestone, quicklime, slaked lime, and slag generated in ironworks. [5] The method for producing sintered ore according to any one of [1] to [4], wherein the frequency of the microwave is 2.4 GHz to 2.5 GHz. [Effect of the invention]
根據本發明,包含以FeO換算為3.0質量%以上的磁鐵礦的燒結原料可獲得高的介電加熱性能,因此能夠藉由微波以更短時間高效率地將燒結原料進行加熱,從而能夠製造燒結礦。According to the present invention, since the sintered raw material containing 3.0% by mass or more of magnetite in terms of FeO can obtain high dielectric heating performance, the sintered raw material can be efficiently heated by microwaves in a shorter time, and it is possible to manufacture Sinter.
以下,一邊參照圖式一邊對本發明的燒結礦的製造方法的實施方式詳細地進行說明。再者,以下所示的實施方式是本發明的實施方式的一例,且本發明不限定於該些實施方式而解釋。Hereinafter, embodiment of the manufacturing method of the sintered ore of this invention is demonstrated in detail, referring drawings. In addition, embodiment shown below is an example of embodiment of this invention, and this invention is not limited to these embodiment, and is interpreted.
[燒結礦製造裝置] 圖1是表示可實施本實施方式的燒結礦的製造方法的燒結礦製造裝置的一例的示意圖。燒結原料裝填至燒結原料供給裝置1中。燒結原料自燒結原料供給裝置1連續地裝入至環形移動式托板(pallet)2中,形成燒結原料的裝入層。自微波照射裝置3照射微波,將燒結原料的裝入層進行加熱,藉由液相燒結使燒結原料成塊而製造燒結礦。 [Sinter manufacturing equipment] FIG. 1 is a schematic diagram showing an example of a sintered ore manufacturing apparatus capable of implementing the sintered ore manufacturing method of this embodiment. The sintering raw material is loaded into the sintering raw material supply device 1 . The sintering raw material is continuously charged from the sintering raw material supply device 1 into an annular movable pallet (pallet) 2 to form a charging layer of the sintering raw material. Microwaves are irradiated from the microwave irradiation device 3 to heat the loaded layer of the sintering raw material, and the sintering raw material is agglomerated by liquid phase sintering to produce sintered ore.
[燒結原料] 燒結原料包含作為鐵源的鐵礦石、及發揮熔劑作用的助熔劑。燒結原料中亦可包含煉鐵廠內所產生的灰塵或燒結礦、矽石。 [Sintering raw material] The raw materials for sintering include iron ore as an iron source and a flux functioning as a flux. Dust, sintered ore, and silica generated in ironworks may also be included in the sintering raw materials.
燒結原料中,為了進一步以適當比例含有磁鐵礦,亦可混合包含磁鐵礦的鐵礦石、包含磁鐵礦的燒結礦及煉鐵廠內所產生的灰塵的1種以上。所謂適當比例的調配,是指磁鐵礦以FeO換算為3.0質量%以上的量。在磁鐵礦以FeO換算小於3.0質量%的情況下,若使用頻率為2.4 GHz~2.5 GHz的微波,則加熱至規定溫度需要長時間的照射,因此欠佳。另外,較佳為磁鐵礦以FeO換算為10.0質量%以下。在調配比例以FeO換算超過10.0質量%的情況下,要增加以赤鐵礦為主成分的鐵礦石以外的原料的調配量,因此燒結原料成本變高。更佳的範圍為4.0質量%以上且8.0質量%以下。另外,燒結原料較佳為不事先藉由造粒或加壓成型等來成塊。這是因為,在以成塊物為加熱對象的情況下,微波會隨著穿透距離而衰減,成塊物的內部的加熱效率有可能降低。另外,在未成塊的情況下,與一般的使用焦炭的燒結法不同,有無需供給空氣的優點,在造粒或成型時使用水分來成塊的情況下,由於水分的蒸發熱而有需要多餘熱量的缺點。In order to further contain magnetite in an appropriate ratio in the raw material for sintering, one or more of iron ore containing magnetite, sintered ore containing magnetite, and dust generated in ironworks may be mixed. The blending of an appropriate ratio means that the magnetite is 3.0% by mass or more in terms of FeO. When the magnetite is less than 3.0% by mass in terms of FeO, it is not preferable to use microwaves with a frequency of 2.4 GHz to 2.5 GHz since long-term irradiation is required for heating to a predetermined temperature. Moreover, it is preferable that magnetite is 10.0 mass % or less in conversion of FeO. When the compounding ratio exceeds 10.0% by mass in terms of FeO, the compounded amount of raw materials other than iron ore containing hematite as a main component will increase, and thus the raw material cost for sintering will increase. A more preferable range is 4.0 mass % or more and 8.0 mass % or less. In addition, it is preferable that the sintered raw material is not formed into a block by granulation or press molding in advance. This is because, when an agglomerated object is used as a heating object, microwaves attenuate with the penetration distance, and the heating efficiency inside the agglomerated object may decrease. In addition, in the case of non-agglomeration, unlike the general sintering method using coke, there is an advantage that air supply is not required, and in the case of using moisture to form agglomerates during granulation or molding, there is a need for excess due to the evaporation heat of moisture. The disadvantage of heat.
[鐵礦石] 鐵礦石的主成分是氧化鐵,包含赤鐵礦(hematite、Fe 2O 3)、磁鐵礦(magnetite、Fe 3O 4)。本實施方式中,使用粒徑8 mm以下的粉狀鐵礦石作為鐵礦石。 [Iron Ore] The main component of iron ore is iron oxide, including hematite (Fe 2 O 3 ) and magnetite (magnetite, Fe 3 O 4 ). In this embodiment, powdery iron ore having a particle size of 8 mm or less is used as iron ore.
[赤鐵礦] 赤鐵礦(hematite、Fe 2O 3)是在高爐法中常用作主原料的氧化鐵。赤鐵礦的顏色是紅褐色或黑色,廣泛分布在岩石或土壤中。在現代的高爐法中,赤鐵礦是與助熔劑或焦炭混合而進行燒結,藉此作為燒結礦加以使用。但是,赤鐵礦的介電常數低,若僅有赤鐵礦則難以利用2.4 GHz~2.5 GHz的微波來加熱。本實施例中是使用以赤鐵礦為主成分的粉狀鐵礦石中含有75質量%~99質量%的赤鐵礦的原料。 [Hematite] Hematite (hematite, Fe 2 O 3 ) is an iron oxide commonly used as a main raw material in the blast furnace process. The color of hematite is reddish brown or black, and it is widely distributed in rocks or soil. In the modern blast furnace method, hematite is mixed with flux or coke and sintered, thereby being used as sinter. However, the dielectric constant of hematite is low, and it is difficult to heat with microwaves of 2.4 GHz to 2.5 GHz if only hematite is used. In the present example, a raw material containing 75% by mass to 99% by mass of hematite in powdered iron ore mainly composed of hematite was used.
[磁鐵礦] 磁鐵礦(magnetite、Fe 3O 4)是氧化鐵的一種。基本上而言,在世界範圍內能夠採集的大部分為低品質。具有高的介電加熱性能,容易利用微波進行加熱。 [Magnetite] Magnetite (magnetite, Fe 3 O 4 ) is a type of iron oxide. Basically, most of what can be collected worldwide is low quality. It has high dielectric heating performance and is easy to use microwave for heating.
本實施方式中的燒結礦是將包含鐵礦石等含鐵原料及助熔劑的燒結原料進行燒結而製造的燒結礦。燒結礦包含磁鐵礦。另外,返礦是燒結礦的製造過程中所獲得的小於製品粒徑的燒結礦,可再次添加至燒結原料中。另外,灰塵是煉鐵廠內所產生的包含Fe的灰塵,例如可使用鐵銹屑、轉爐灰塵、高爐灰塵。另外,亦可調配矽石以調整鹼度。The sintered ore in this embodiment is a sintered ore produced by sintering a sintered raw material containing iron-containing raw materials such as iron ore and a flux. Sintered ore contains magnetite. In addition, the returned ore is the sintered ore obtained in the production process of the sintered ore, which is smaller than the particle size of the product, and can be added to the sintered raw material again. In addition, dust is dust containing Fe generated in an ironworks, and for example, rust scraps, converter dust, and blast furnace dust can be used. In addition, silica can also be added to adjust the alkalinity.
[助熔劑] 本實施方式中的助熔劑是包含如石灰石、生石灰、熟石灰般藉由加熱會成為CaO的物質、或者含有CaO的煉鐵廠內所產生的礦渣的原料,發揮使燒結原料中的氧化鐵彼此相互熔解而加固的作用。關於助熔劑的調配量,較佳為以燒結原料的CaO/SiO 2成為1.7~2.3的方式進行調配。所謂煉鐵廠內所產生的包含CaO的礦渣,是指例如高爐內所產生的高爐礦渣、或製鋼步驟中所產生的製鋼礦渣。 [Fluxing agent] The fluxing agent in this embodiment is a raw material containing a substance that becomes CaO by heating such as limestone, quicklime, and slaked lime, or slag generated in an ironworks containing CaO, and exerts the flux in the sintering raw material. The role of iron oxides to melt and strengthen each other. It is preferable to prepare so that CaO/ SiO2 of a sintering raw material may become 1.7-2.3 about the compounding quantity of a flux. The slag containing CaO generated in an ironworks refers to, for example, blast furnace slag generated in a blast furnace or steelmaking slag generated in a steelmaking step.
[燒結] 燒結原料中所分散的磁鐵礦具有高的介電加熱性能,因此藉由微波進行加熱,經加熱的磁鐵礦成為熱源而將燒結原料整體進行加熱。助熔劑中的CaO及氧化鐵被加熱而熔融,使粉狀的氧化鐵成為塊狀。 [sintering] The magnetite dispersed in the sintering raw material has high dielectric heating performance, so it is heated by microwaves, and the heated magnetite becomes a heat source to heat the whole sintering raw material. CaO and iron oxide in the flux are heated and melted, and powdery iron oxide is formed into lumps.
[加熱溫度] 利用微波的燒結原料的加熱溫度設為1000℃以上。作為加熱溫度的上限,較佳為設為1350℃以下。這是因為,若加熱溫度高於1350℃,則赤鐵礦會變為磁鐵礦,且當溫度下降而再次成為赤鐵礦時,會成為還原粉化性(reduction disintegration index,RDI)極差的二次赤鐵礦。進而,加熱溫度更佳為設為1200℃以上且1300℃以下。 [heating temperature] The heating temperature of the raw materials for sintering by microwaves is set to 1000° C. or higher. As an upper limit of heating temperature, it is preferable to set it as 1350 degreeC or less. This is because, if the heating temperature is higher than 1350°C, hematite will turn into magnetite, and when the temperature drops and becomes hematite again, it will become extremely poor in reduction disintegration index (RDI). secondary hematite. Furthermore, it is more preferable to set heating temperature as 1200 degreeC or more and 1300 degreeC or less.
[微波照射裝置] 微波是電磁波的一種。根據國際安全管理規則(International Safety Management,ISM)或電波法,不具有電磁波的大規模的洩漏防止裝置的裝置中可使用的頻帶受到限制。 [Microwave irradiation device] Microwaves are a type of electromagnetic waves. According to the International Safety Management (ISM) or the radio wave law, the usable frequency band is limited in a device that does not have a large-scale leakage prevention device for electromagnetic waves.
磁控管是小型且微波爐等中所使用的通用的微波產生裝置,所述磁控管的頻率包含被視為ISM基本頻率的2.4 GHz~2.5 GHz的範圍。在ISM基本頻率所指定的範圍內,用以防止與其他頻率的電磁波的干擾的限制並不嚴格,因此只要可使用2.4 GHz~2.5 GHz的範圍的微波,則可使用比迴旋管廉價的磁控管來製造燒結礦,因此燒結礦的製造設備變得廉價。進而,若為2.4 GHz~2.5 GHz的微波,則亦無需使用大規模的電波洩漏防止設備,因此能夠利用小型且廉價的設備製造燒結礦。A magnetron is a small, general-purpose microwave generator used in microwave ovens and the like, and the frequency of the magnetron includes a range of 2.4 GHz to 2.5 GHz, which is regarded as the fundamental frequency of ISM. Within the range specified by the ISM basic frequency, there are no strict restrictions to prevent interference with electromagnetic waves of other frequencies. Therefore, as long as microwaves in the range of 2.4 GHz to 2.5 GHz can be used, magnetrons that are cheaper than gyrotrons can be used. Pipes are used to make sintered ore, so the manufacturing equipment of sintered ore becomes cheap. Furthermore, if it is a microwave of 2.4 GHz to 2.5 GHz, it is not necessary to use a large-scale radio wave leakage prevention facility, so it is possible to manufacture sintered ore with small and inexpensive facilities.
作為本實施方式中的微波照射裝置的形態,可列舉圖1所示的穿隧型等。但是,只要為可對燒結原料的裝入層照射微波的形狀、配置即可,並不僅限定於本實施方式中所例示的形狀。As a form of the microwave irradiation apparatus in this embodiment, the tunnel type shown in FIG. 1 etc. are mentioned. However, it is not limited to the shapes exemplified in this embodiment as long as it has a shape and arrangement in which microwaves can be irradiated to the loading layer of the sintering raw material.
本實施方式的燒結礦的製造方法中,即便在使用2.4 GHz~2.5 GHz的微波的情況下,亦可照射所述微波而將燒結原料以135秒左右的短時間加熱至1000℃以上,藉由液相燒結使燒結原料成塊而製造燒結礦。若使用微波照射裝置長度6為40~50 m的微波照射裝置,則能夠使托板速度成為20 m/min,因此若將托板寬度4設為4~5 m、托板裝入層高度5設為100 mm,則可獲得300萬噸/年的燒結礦的生產量。如此,若可使用微波將燒結原料進行加熱而製造燒結礦,則可不使用粉焦炭等而製造燒結礦,從而亦能夠削減伴隨燒結礦的製造的CO 2的產生量。 [實施例] In the method for producing sintered ore according to this embodiment, even when microwaves of 2.4 GHz to 2.5 GHz are used, the sintered raw material can be heated to 1000° C. or higher in a short time of about 135 seconds by irradiating the microwaves. Liquid-phase sintering agglomerates sintered raw materials to produce sintered ore. If a microwave irradiation device with a microwave irradiation device length 6 of 40-50 m is used, the pallet speed can be made 20 m/min. Therefore, if the pallet width 4 is set to 4-5 m and the If it is set to 100 mm, a production capacity of 3 million tons/year of sintered ore can be obtained. In this way, if sintered ore can be produced by heating the sintered raw material using microwaves, the sintered ore can be produced without using powdered coke or the like, and the amount of CO 2 generated accompanying the production of sintered ore can also be reduced. [Example]
[實驗1] 首先,進行使用磁鐵礦試劑的實驗。表1中示出調配。磁鐵礦試劑是按照以FeO換算成為3~10質量%的方式調整。藉由化學分析測定原料中的磁鐵礦量作為原料中的FeO量。將測定值示於表1。 [Experiment 1] First, experiments using magnetite reagents were performed. Formulations are shown in Table 1. The magnetite reagent is adjusted so that it becomes 3-10 mass % in conversion of FeO. The amount of magnetite in the raw material was determined by chemical analysis as the amount of FeO in the raw material. Table 1 shows the measured values.
[表1]
原料中的CaO及SiO 2是使用試劑,調配模擬實際操作的量。SiO 2是以調整下一步驟的高爐中的礦渣成分,控制鹼度為目的而調配。 The CaO and SiO2 in the raw materials are the amount used to simulate the actual operation by using reagents. SiO 2 is prepared for the purpose of adjusting the composition of the slag in the blast furnace in the next step and controlling the alkalinity.
各試樣的質量設為合計36 g~38 g,混合中使用研缽及研棒,充分混合直至目視下試驗體的顏色變得均勻為止。各樣品是一邊輕輕地振實一邊填充至自氧化鋁坩堝8的上端起約2 mm左右的高度。將裝置概要示於圖2。使用如下裝置,即,在微波爐7內放置有氧化鋁坩堝8,在熱電偶插入高度12為18 mm的位置裝入有熱電偶9的裝置。坩堝上表面側內徑10設為φ30 mm,坩堝高度11設為27 mm。The mass of each sample was set to 36 g to 38 g in total, and a mortar and a pestle were used for mixing, and the mixture was sufficiently mixed until the color of the test body became uniform visually. Each sample was filled to a height of about 2 mm from the upper end of the alumina crucible 8 while lightly vibrating. The outline of the device is shown in FIG. 2 . An apparatus was used in which alumina crucible 8 was placed in microwave oven 7 and thermocouple 9 was incorporated at a position where thermocouple insertion height 12 was 18 mm. The inner diameter 10 on the upper surface side of the crucible was set to φ30 mm, and the crucible height 11 was set to 27 mm.
微波的頻率設為2.45 GHz,加熱中以升溫速度成為1000℃/min的方式以程式控制微波的輸出(瓦特數)。達到1300℃後,中止利用微波的加熱而連同氧化鋁坩堝8一起進行空氣冷卻。The frequency of the microwave was set to 2.45 GHz, and the output (wattage) of the microwave was controlled by a program so that the temperature increase rate became 1000° C./min during heating. After reaching 1300° C., the heating by the microwave was stopped, and the alumina crucible 8 was air-cooled together.
將實驗結果示於表2。有無燒結是以抗壓強度及有無氣孔的再排列為基準而進行判斷。另外,抗壓強度是使用精密電子萬能材料試驗機(Autograph)(速度:1 mm/min)來測定。由於用作高爐原料的燒結礦的抗壓強度為2 MPa~4 MPa,故而若具有2 MPa以上的強度,則判斷為實際應用上合格。The experimental results are shown in Table 2. The presence or absence of sintering is judged based on the compressive strength and the rearrangement of pores. In addition, the compressive strength was measured using the precision electronic universal testing machine (Autograph) (speed: 1 mm/min). Since the compressive strength of sintered ore used as a raw material for a blast furnace is 2 MPa to 4 MPa, it is judged to be acceptable for practical use if it has a strength of 2 MPa or more.
[表2]
實施例1~實施例3中,燒結原料升溫至1000℃以上。剛試驗後的實施例1~實施例3的樣品為熔融狀態。圖3的(b)~圖3的(d)中示出實施例1~實施例3的加熱後的坩堝上表面照片(上圖)及燒結組織觀察照片(下圖)。如圖3所示,可知實施例1(b)、實施例2(c)、實施例3(d)熔融,且就氣孔進行了再排列來看,進行了燒結反應。實施例1~實施例3中,磁鐵礦以FeO換算分別包含3.3質量%、6.4質量%、9.4質量%。因此,藉由頻率2.45 GHz的微波將該些原料加熱,燒結原料整體達到1000℃以上,進行燒結反應而成塊,從而可製造具有規定強度的燒結礦。In Examples 1 to 3, the temperature of the raw materials for sintering was raised to 1000° C. or higher. The samples of Examples 1 to 3 immediately after the test were in a molten state. Fig. 3(b) to Fig. 3(d) show photographs of the upper surface of the crucible after heating in Examples 1 to 3 (upper figure) and observation photographs of the sintered structure (lower figure). As shown in FIG. 3 , it can be seen that Example 1(b), Example 2(c), and Example 3(d) were melted, and the sintering reaction proceeded in view of rearrangement of pores. In Examples 1 to 3, magnetite contained 3.3% by mass, 6.4% by mass, and 9.4% by mass in terms of FeO, respectively. Therefore, these raw materials are heated by microwaves with a frequency of 2.45 GHz, and the whole raw materials are sintered to a temperature of 1000°C or higher, and the sintering reaction proceeds to form agglomerates, thereby producing sintered ore with a predetermined strength.
比較例1中,溫度的上升在中途停止,亦未觀測到微波的吸收,因此中止試驗。如圖3的(a)所示,可知比較例1的試驗後的試驗體保持粉末狀態不變,組織觀察時,比較例1中氣孔亦未再排列,原本的礦石的粒子直接殘留,未進行燒結反應。可認為,由於比較例1中未添加磁鐵礦,磁鐵礦以FeO換算僅含有0.2質量%,故而若為頻率為2.45 GHz微波則無法加熱,因此未進行燒結反應。In Comparative Example 1, the temperature rise stopped halfway, and microwave absorption was not observed, so the test was terminated. As shown in Figure 3(a), it can be seen that the test body of Comparative Example 1 remains in a powder state after the test, and when the microstructure is observed, the pores in Comparative Example 1 are not rearranged, and the original ore particles remain as they are, without further investigation. sintering reaction. It is considered that since no magnetite was added in Comparative Example 1 and the magnetite contained only 0.2% by mass in terms of FeO, the sintering reaction did not proceed because microwaves with a frequency of 2.45 GHz could not be heated.
[實驗2] 接下來,以工業上所使用的磁鐵礦精礦及鐵銹屑為原料而使用合計36 g~38 g的試樣。實施例4~實施例6是以實施例1中確認到燒結的調配為參考,設為以FeO換算為3質量%的調配率。另外,參考例1中使用與實施例5相同的原料,填充事先進行造粒並乾燥而成的原料。表3中示出比較例2、實施例4~實施例6及參考例1的調配。表4中示出各原料中的Fe元素的存在形態的比例。針對該些試樣以3 kW照射頻率2.45 GHz的微波而進行加熱。 [Experiment 2] Next, a total of 36 g to 38 g of samples was used using industrially used magnetite concentrate and rust scraps as raw materials. In Examples 4 to 6, the blending in which sintering was confirmed in Example 1 was used as a reference, and the blending rate was 3% by mass in terms of FeO. In addition, in Reference Example 1, the same raw material as in Example 5 was used, and the raw material obtained by granulating and drying in advance was filled. Table 3 shows the preparation of Comparative Example 2, Examples 4 to 6, and Reference Example 1. Table 4 shows the ratio of the existing form of Fe element in each raw material. These samples were heated by irradiating microwaves with a frequency of 2.45 GHz at 3 kW.
[表3]
[表4]
圖4中示出所計測的溫度曲線。未調配磁鐵礦精礦及鐵銹屑的比較例2中,磁鐵礦以FeO換算僅含有0.7質量%,因此直至達到燒結開始的1000℃為止需要約180秒(3分鐘)。另一方面,調配有磁鐵礦精礦或鐵銹屑的實施例4~實施例6中,包含磁鐵礦3.0質量%以上,因此升溫速度快,以135秒(2分鐘15秒)以下達到1000℃而燒結。另外,參考例1中,升溫速度高於比較例2,但若與使用相同原料的實施例5相比,則成為升溫速度非常低的結果。The measured temperature profile is shown in FIG. 4 . In Comparative Example 2 in which no magnetite concentrate or rust was prepared, the magnetite contained only 0.7% by mass in terms of FeO, and therefore it took about 180 seconds (3 minutes) to reach 1000° C. at which sintering started. On the other hand, in Examples 4 to 6 in which magnetite concentrate or iron rust was blended, magnetite was contained in an amount of 3.0% by mass or more, so the heating rate was fast, reaching 1000°C in 135 seconds (2 minutes and 15 seconds). °C for sintering. In addition, in Reference Example 1, the rate of temperature increase was higher than that of Comparative Example 2, but when compared with Example 5 using the same raw material, the rate of temperature increase was very low as a result.
1:燒結原料供給裝置 2:托板 3:微波照射裝置 4:托板寬度 5:托板裝入層高度 6:微波照射裝置長度 7:微波爐 8:氧化鋁坩堝 9:熱電偶 10:坩堝上表面側內徑(實施例:φ30 mm) 11:坩堝高度(實施例:27 mm) 12:熱電偶插入高度(實施例:18 mm) 1: Sintering raw material supply device 2: pallet 3: Microwave irradiation device 4: Pallet width 5: Pallet loading layer height 6: Length of microwave irradiation device 7: Microwave oven 8: Alumina crucible 9: Thermocouple 10: Inner diameter of the upper surface of the crucible (Example: φ30 mm) 11: Crucible height (Example: 27 mm) 12: Thermocouple insertion height (Example: 18 mm)
圖1是表示可實施本發明的燒結礦的製造方法的燒結機的一例的示意圖。 圖2的(a)是表示本發明的一實驗例中的燒結礦製造的示意圖。圖2的(b)是表示氧化鋁坩堝形狀及熱電偶的配置的示意圖。 圖3是加熱後的坩堝上表面照片(上圖)及燒結組織觀察照片(下圖)。(a)是比較例1,(b)是實施例1,(c)是實施例2,及(d)是實施例3。 圖4是表示實驗2中的微波照射時間與燒結原料的溫度變化的關係的圖。 FIG. 1 is a schematic diagram showing an example of a sintering machine capable of implementing the method for producing sintered ore of the present invention. (a) of FIG. 2 is a schematic diagram which shows the production of sintered ore in one experimental example of this invention. (b) of FIG. 2 is a schematic diagram showing the shape of an alumina crucible and the arrangement of thermocouples. Figure 3 is the photo of the upper surface of the crucible after heating (upper picture) and the observation photo of the sintered structure (lower picture). (a) is Comparative Example 1, (b) is Example 1, (c) is Example 2, and (d) is Example 3. FIG. 4 is a graph showing the relationship between the microwave irradiation time and the temperature change of the sintered raw material in Experiment 2. FIG.
1:燒結原料供給裝置 1: Sintering raw material supply device
2:托板 2: pallet
3:微波照射裝置 3: Microwave irradiation device
4:托板寬度 4: Pallet width
5:托板裝入層高度 5: Pallet loading layer height
6:微波照射裝置長度 6: Length of microwave irradiation device
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