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JP7782667B2 - Sinter manufacturing method - Google Patents
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JP7782667B2 - Sinter manufacturing method - Google Patents

Sinter manufacturing method

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JP7782667B2
JP7782667B2 JP2024502141A JP2024502141A JP7782667B2 JP 7782667 B2 JP7782667 B2 JP 7782667B2 JP 2024502141 A JP2024502141 A JP 2024502141A JP 2024502141 A JP2024502141 A JP 2024502141A JP 7782667 B2 JP7782667 B2 JP 7782667B2
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carbonaceous material
sintering
combustion
sintered ore
carbonaceous
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JPWO2024084749A1 (en
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友司 岩見
慎平 藤原
隆英 樋口
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JFE Steel Corp
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/14Agglomerating; Briquetting; Binding; Granulating
    • C22B1/16Sintering; Agglomerating
    • C22B1/20Sintering; Agglomerating in sintering machines with movable grates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B53/00Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
    • C10B53/02Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of cellulose-containing material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B53/00Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form
    • C10B53/07Destructive distillation, specially adapted for particular solid raw materials or solid raw materials in special form of solid raw materials consisting of synthetic polymeric materials, e.g. tyres
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L5/00Solid fuels
    • C10L5/02Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
    • C10L5/04Raw material of mineral origin to be used; Pretreatment thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L5/00Solid fuels
    • C10L5/40Solid fuels essentially based on materials of non-mineral origin
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/14Agglomerating; Briquetting; Binding; Granulating
    • C22B1/24Binding; Briquetting ; Granulating
    • C22B1/2406Binding; Briquetting ; Granulating pelletizing
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/14Agglomerating; Briquetting; Binding; Granulating
    • C22B1/24Binding; Briquetting ; Granulating
    • C22B1/2413Binding; Briquetting ; Granulating enduration of pellets
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B1/00Preliminary treatment of ores or scrap
    • C22B1/14Agglomerating; Briquetting; Binding; Granulating
    • C22B1/24Binding; Briquetting ; Granulating
    • C22B1/242Binding; Briquetting ; Granulating with binders
    • C22B1/244Binding; Briquetting ; Granulating with binders organic
    • C22B1/245Binding; Briquetting ; Granulating with binders organic with carbonaceous material for the production of coked agglomerates

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Geology (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

本発明は、固体燃料としての炭材を含む焼結配合原料を造粒して焼結用造粒原料を作製し、その焼結用造粒原料を焼結して焼結鉱を得る焼結鉱の製造方法に関する。 The present invention relates to a method for producing sintered ore, which comprises granulating a sintering compound raw material containing carbonaceous material as a solid fuel to produce granulated raw material for sintering, and sintering the granulated raw material for sintering to obtain sintered ore.

焼結鉱の製造プロセスでは、鉄鉱石とフラックス、および固体燃料としての炭材を混合したものを焼結機内において、その炭材の燃焼熱を用いて焼き固めて焼結鉱を製造している。一般的に炭材としては粉コークスが使用されるが、原料炭の価格変動やコークス製造設備のトラブル等へのリスク分散として、粉コークス以外の無煙炭等が使用されることもある。 In the sintering process, iron ore, flux, and carbonaceous material used as solid fuel are mixed in a sintering machine and then baked using the heat from the combustion of the carbonaceous material to produce sintered ore. Generally, coke breeze is used as the carbonaceous material, but anthracite and other coals are sometimes used to diversify the risk of fluctuations in the price of raw coal and problems with coke production equipment.

一方、近年の環境保全への意識の高まりを受け、リスク分散等の考え方とは別に環境への負担を低減するという意図を以って、炭材の多様化が進んでいる。その一例として、特許文献1では、亜瀝青炭や褐炭を想定した焼結鉱製造用の炭材が提案されている。この炭材は、反応開始温度が550℃以下、揮発分(VM)が1.0%以上、水素と炭素の原子数比(H/C)が0.040以上、水銀圧入法で測定される孔径0.1~10μmの気孔量が50mm/g以上という性質を有している。また、特許文献2では、4.0mass%以上の結晶水を含有する高結晶水鉄鉱石を30%以上使用した際に、燃焼開始温度が450℃未満である固体燃料を10mass%以上含む焼結原料の使用が提案されている。 Meanwhile, with the recent rise in environmental awareness, diversification of carbonaceous materials is progressing with the intention of reducing the burden on the environment, regardless of risk diversification. As an example, Patent Document 1 proposes a carbonaceous material for sintered ore production, assuming subbituminous coal or lignite. This carbonaceous material has the following properties: a reaction initiation temperature of 550°C or less, a volatile matter (VM) of 1.0% or more, a hydrogen-to-carbon atomic ratio (H/C) of 0.040 or more, and a pore volume of 0.1 to 10 μm in diameter measured by mercury porosimetry of 50 mm 3 /g or more. Patent Document 2 also proposes the use of a sintering raw material containing 10 mass% or more of solid fuel with a combustion initiation temperature of less than 450°C when using 30% or more of high-crystallization-water iron ore containing 4.0 mass% or more of crystallization water.

しかし、そのいずれも反応開始温度の上限を定めていることから、焼結鉱製造プロセスにおける歩留の悪化影響を考慮できていない。この点で、特許文献3では、焼結装入層を2段階で形成し、それぞれの表面に点火し焼結を行う2段点火焼結法において、下段側の原料にコークスや無煙炭とそれらよりも燃焼開始温度の低い炭材を用いる方法が提案されている。また、特許文献4では、凝結材として粉コークスや無煙炭に燃焼開始温度の低い炭材を合計炭素分の25~75%範囲で配合、かつ低燃焼開始温度炭材、高燃焼開始温度炭材の少なくともいずれか一方を造粒工程後半で添加する方法が提案されている。However, all of these methods set an upper limit on the reaction initiation temperature, and therefore fail to take into account the negative impact on yield in the sinter ore production process. In this regard, Patent Document 3 proposes a two-stage ignition sintering method in which a sintered charge bed is formed in two stages, and sintering is carried out by igniting the surfaces of each stage. This method uses coke or anthracite as the raw material for the lower stage, along with a carbonaceous material with a lower combustion initiation temperature than coke or anthracite, in an amount ranging from 25 to 75% of the total carbon content, and adds at least one of a low combustion initiation temperature carbonaceous material and a high combustion initiation temperature carbonaceous material in the latter half of the granulation process.

特許第4681688号公報Patent No. 4681688 特許第4837799号公報Patent No. 4837799 特開2020-186436号公報Japanese Patent Application Laid-Open No. 2020-186436 特開2022-033594号公報Japanese Patent Application Laid-Open No. 2022-033594

しかしながら、特許文献3に開示された方法では、2段点火焼結法という前提があり、一般的な焼結法に活用することはできなかった。また、特許文献4に開示された方法では、低燃焼開始温度の炭材にも種類があり、その燃焼開始温度は様々であることから、一律に炭素分で整理を行うことにはリスクがあった。However, the method disclosed in Patent Document 3 is based on the premise of a two-stage ignition sintering method, and therefore could not be used for general sintering methods. Furthermore, with the method disclosed in Patent Document 4, there are different types of carbonaceous materials with low combustion initiation temperatures, and these combustion initiation temperatures vary, so there was a risk in uniformly sorting by carbon content.

本発明の目的は、上記の問題点を解決して、固体燃料としての炭材を含む焼結配合原料を造粒して焼結用造粒原料を作製し、その焼結用造粒原料を焼結して焼結鉱を得る焼結鉱の製造方法において、燃焼開始温度の低い炭材使用時の歩留低下を防止することができる焼結鉱の製造方法を提案することにある。 The object of the present invention is to solve the above problems and propose a method for producing sintered ore that can prevent a decrease in yield when using carbonaceous material with a low combustion start temperature in a method for producing sintered ore by granulating a sintering compound raw material containing carbonaceous material as a solid fuel to produce granulated raw material for sintering, and then sintering the granulated raw material for sintering to obtain sintered ore.

本発明の焼結鉱の製造方法は、固体燃料としての炭材を含む焼結配合原料を造粒して焼結用造粒原料を作製し、その焼結用造粒原料を焼結して焼結鉱を得る焼結鉱の製造方法において、前記炭材として、少なくとも2種類以上の炭材を配合した炭材であって、その燃焼開始温度の加重平均が550℃以上であるものを用いて焼結することを特徴とする、焼結鉱の製造方法である。 The method for producing sintered ore of the present invention involves granulating a sintering blended raw material containing a carbonaceous material as a solid fuel to produce a granulated raw material for sintering, and then sintering the granulated raw material for sintering to obtain sintered ore, characterized in that the carbonaceous material used is a blend of at least two types of carbonaceous material, and the weighted average of the combustion start temperatures is 550°C or higher.

なお、前記のように構成される本発明に係る焼結鉱の製造方法においては、
(1)前記配合する炭材に燃焼開始温度が550℃未満のものが含まれていること、
(2)前記燃焼開始温度が550℃未満の炭材が、化石燃料を除く有機系資源、あるいは前記有機系資源を原料として製造されたものを含むこと、
(3)前記燃焼開始温度が550℃未満の炭材が、バイオマス炭、無煙炭、廃プラスチック炭、褐炭や亜瀝青炭を原料とするコークスであること、
(4)配合後の炭材の全量が造粒工程の前に添加されること、
がより好ましい解決手段となるものと考えられる。
In the method for producing sintered ore according to the present invention configured as described above,
(1) The carbonaceous material to be blended includes one having a combustion start temperature of less than 550°C;
(2) The carbonaceous material having a combustion start temperature of less than 550°C includes an organic resource other than fossil fuel, or a material produced using the organic resource as a raw material;
(3) The carbonaceous material having a combustion start temperature of less than 550°C is a coke made from biomass coal, anthracite, waste plastic coal, lignite, or subbituminous coal;
(4) The entire amount of the blended carbonaceous material is added before the granulation process;
This is considered to be a more preferable solution.

本発明の焼結鉱の製造方法によれば、炭材として、少なくとも2種類以上の炭材を配合した炭材であって、その燃焼開始温度の加重平均が550℃以上であるものを用いて焼結することで、焼結鉱に配合して使用する際の歩留減少を抑制することができる。 According to the method for producing sintered ore of the present invention, by sintering a carbonaceous material that is a blend of at least two types of carbonaceous material and has a weighted average combustion start temperature of 550°C or higher, it is possible to suppress yield reduction when blended into sintered ore and used.

本発明の焼結鉱の製造方法で用いる焼結鉱の製造設備の一実施形態を示す模式図である。1 is a schematic diagram showing an embodiment of a sintered ore manufacturing facility used in a sintered ore manufacturing method of the present invention. FIG. 実施例における成品歩留と燃焼開始温度の加重平均との関係を示すグラフである。1 is a graph showing the relationship between product yield and weighted average of combustion initiation temperature in Examples. 炭材造粒前添加および炭材造粒後半添加について、それぞれの成品歩留を比較して示すグラフである。1 is a graph showing a comparison of product yields between addition before carbonaceous material granulation and addition after carbonaceous material granulation.

以下、本発明の実施の形態について具体的に説明する。なお、以下の実施形態は、本発明の技術的思想を具体化するための装置や方法を例示するものであり、構成を下記のものに特定するものでない。すなわち、本発明の技術的思想は、特許請求の範囲に記載された技術的範囲内において、種々の変更を加えることができる。 The following provides a detailed description of embodiments of the present invention. Note that the following embodiments are intended to exemplify devices and methods that embody the technical concepts of the present invention, and are not intended to limit the configuration to those described below. In other words, the technical concepts of the present invention can be modified in various ways within the technical scope described in the claims.

<本発明の焼結鉱の製造方法で用いる焼結鉱の製造設備について>
図1は、本発明の焼結鉱の製造方法で用いる焼結鉱の製造設備1の一実施形態を示す模式図である。焼結鉱の製造設備1は、造粒装置であるドラムミキサー2と、焼結機3と、破砕機4と、クーラー5と、篩分装置6とを有する。鉄含有原料、副原料および炭材やコークス粉といった凝結材を含む焼結原料は、造粒水が添加されてドラムミキサー2で造粒される。造粒された焼結用造粒原料は焼結機3に搬送される。
<Regarding the sintered ore manufacturing equipment used in the sintered ore manufacturing method of the present invention>
1 is a schematic diagram showing one embodiment of a sinter ore production facility 1 used in the sinter ore production method of the present invention. The sinter ore production facility 1 has a drum mixer 2, which is a granulating device, a sinter machine 3, a crusher 4, a cooler 5, and a sieving device 6. Sinter raw materials including iron-containing raw materials, auxiliary raw materials, and coagulating agents such as carbonaceous material and coke powder are granulated in the drum mixer 2 after granulation water is added. The granulated raw materials for sintering are transported to the sinter machine 3.

焼結機3は、例えば、ドワイトロイド式の焼結機である。焼結機3は、焼結原料供給装置11と、無端移動式のパレット台車12と、点火炉13と、ウインドボックス14とを有する。造粒された焼結用造粒原料は、焼結原料供給装置11からパレット台車12に装入され、焼結用造粒原料の装入層が形成される。点火炉13で装入層表層に含まれる凝結材が点火されるとともに、ウインドボックス14を通じて装入層内の空気が下方へ吸引されることで、装入層内の燃焼溶融帯が装入層の下方に移動される。この燃焼溶融帯の移動により、装入層が焼結されて焼結ケーキとなる。 The sintering machine 3 is, for example, a Dwight Lloyd type sintering machine. The sintering machine 3 has a sintering raw material supply device 11, an endless moving pallet cart 12, an ignition furnace 13, and a wind box 14. Granulated sintering raw material is loaded from the sintering raw material supply device 11 onto the pallet cart 12, forming a sintering raw material bed. The ignition furnace 13 ignites the coagulant contained in the surface layer of the sintering bed, and air within the sintering bed is sucked downward through the wind box 14, moving the combustion and melting zone within the sintering bed below the sintering bed. This movement of the combustion and melting zone sinters the sintering bed into a sintered cake.

ウインドボックス14を通じて装入層内の空気を下方へ吸引する際、装入層の上方から気体燃料および/または酸素を富化した酸素富化空気を供給してもよい。気体燃料は、高炉ガス、コークス炉ガス、転炉ガス、都市ガス、天然ガス、メタンガス、エタンガス、プロパンガスおよびこれらの混合ガスから選ばれるいずれかの可燃性ガスである。 When the air in the sintering bed is sucked downward through the wind box 14, gaseous fuel and/or oxygen-enriched air may be supplied from above the sintering bed. The gaseous fuel is any combustible gas selected from blast furnace gas, coke oven gas, converter gas, city gas, natural gas, methane gas, ethane gas, propane gas, and mixtures thereof.

焼結ケーキは破砕機4によって破砕され、クーラー5で冷却される。焼結ケーキの破砕物は、篩分装置6で粒径5mm以上の焼結鉱と粒径5mm未満の返鉱とに篩分けされる。返鉱は、再び、焼結原料に用いられる。このようにして焼結鉱は生産される。The sinter cake is crushed by crusher 4 and cooled in cooler 5. The crushed sinter cake is sieved in sieving device 6 into sinter ore with a particle size of 5 mm or more and return ore with a particle size of less than 5 mm. The return ore is reused as sinter raw material. In this way, sinter ore is produced.

<本発明の焼結鉱の製造方法について>
本発明の焼結鉱の製造方法の特徴は、固体燃料としての炭材として、少なくとも2種類以上の炭材を配合した炭材であって、その燃焼開始温度の加重平均が550℃以上であるものを用いて焼結する点にある。以下、本発明の特徴となる、本発明の焼結鉱の製造方法で使用する炭材について説明する。
<Regarding the method for producing sintered ore of the present invention>
The method for producing sintered ore according to the present invention is characterized in that the carbonaceous material used as the solid fuel is a blend of at least two types of carbonaceous material, and the weighted average of the combustion start temperatures is 550° C. or higher. The carbonaceous material used in the method for producing sintered ore according to the present invention, which is a characteristic of the present invention, will be described below.

環境負荷低減のための炭材の多様化においては、バイオマス由来の炭材(以下、バイオマス炭)が着目されている。バイオマス炭はその原料となる植物が成長するまでの間に炭酸ガスを吸収するため、そのバイオマス炭を用いた燃料は、カーボンニュートラルの考え方から系外への炭酸ガスの排出量は無い物としてカウントすることができる。これにより、通常粉コークスを使用する鉄鉱石焼結プロセスにおいても、バイオマス炭の使用が検討されている。バイオマス炭の特徴としては、その燃焼開始温度がコークス(600~750℃)と比較して低く、概ね550℃以下である。 In an effort to diversify carbonaceous materials to reduce environmental impact, biomass-derived carbonaceous materials (hereinafter referred to as biomass charcoal) are attracting attention. Because biomass charcoal absorbs carbon dioxide while the plants that serve as its raw material grow, fuels made from biomass charcoal can be counted as carbon-neutral, meaning that no carbon dioxide is emitted outside the system. As a result, the use of biomass charcoal is being considered even in iron ore sintering processes, which typically use coke breeze. A characteristic of biomass charcoal is that its combustion start temperature is lower than that of coke (600-750°C), generally below 550°C.

上述した焼結機3における焼結工程では、鉄鉱石にフラックスと炭材を加え焼結機3上に連続的に装入し、焼結原料の装入層からなる焼結ベッドを形成する。焼結ベッドは上端に点火した後、下端から排ガスを吸引することで炭材の燃焼がベッド上端から下端へ伝播し、その熱を用いて鉄鉱石とフラックスの反応・塊成化がなされる。下層からの排ガス吸引はブロワーを用いて行われており、吸引された排ガスはダクト内を通り、集塵機、脱硫・脱硝設備を経て煙突から排出される。 In the sintering process in the sintering machine 3 described above, flux and carbonaceous material are added to the iron ore and continuously charged onto the sintering machine 3, forming a sintering bed consisting of a layer of sintering raw materials. After igniting the sintering bed at the top, exhaust gas is drawn in from the bottom, causing the combustion of the carbonaceous material to spread from the top to the bottom of the bed, and the heat is used to cause the iron ore and flux to react and form into agglomerates. Exhaust gas is drawn in from the bottom layer using a blower, and the drawn-in exhaust gas passes through a duct, passes through a dust collector, and desulfurization and denitrification equipment before being discharged from the chimney.

前述したとおり、バイオマス炭の特徴はその燃焼開始温度の低さにある。これはバイオマス炭が一般的に焼結工程で使用されている粉コークス(化石燃料由来)と比較し、多孔質でその表面積が非常に高いため、低い温度であっても高い燃焼速度を得られるためであるとされている。したがって、バイオマス炭は、燃焼開始温度が低いが、その後の燃焼速度は高い傾向を示す。As mentioned above, a distinctive feature of biomass charcoal is its low combustion initiation temperature. This is thought to be because, compared to the fine coke (derived from fossil fuels) commonly used in the sintering process, biomass charcoal is porous and has a very high surface area, allowing for a high combustion rate even at low temperatures. Therefore, although biomass charcoal has a low combustion initiation temperature, it tends to have a high subsequent combustion rate.

炭材の燃焼反応は気固反応である。炭材は周囲の気体中の酸素と反応し燃焼している。焼結のように気体が流れている条件での気固反応においては、固体表面にごく薄層のガス境膜と呼ばれる領域が存在する。ガス境膜は外側の乱流の影響を受けず層流が維持されている。炭材の燃焼はガス境膜の外側からガス境膜内を酸素が拡散し、炭材表面に達することで燃焼に使用される。ここで、炭材の燃焼速度が非常に速い場合、周囲の酸素濃度が高い場合でも、ガス境膜内の酸素拡散による酸素供給速度に対し、炭材の燃焼による表面での酸素消費速度が大きくなり、ガス境膜内の酸素濃度が低下する。このため、炭材は不完全燃焼を起こし、一酸化炭素の発生量が増加する。したがって、燃焼速度が非常に速い場合、炭材としての燃焼熱の一部が一酸化炭素として系外に排出されるため、焼結に使用される反応熱が減少することで歩留が低下する。ここで、使用する炭材の燃焼速度を低下させ、燃焼開始温度を550℃以上とすることで、燃焼反応における酸素供給でのガス境膜内拡散律速を解消し、燃焼熱の一部を一酸化炭素として系外へ排出されることを抑制することが可能である。The combustion reaction of carbonaceous materials is a gas-solid reaction. Carbonaceous materials burn by reacting with oxygen in the surrounding gas. In gas-solid reactions under flowing gas conditions, such as sintering, a very thin layer called a gas film exists on the solid surface. The gas film maintains a laminar flow unaffected by external turbulence. Oxygen diffuses from the outside of the gas film through the gas film and reaches the surface of the carbonaceous material, where it is used for combustion. However, if the combustion rate of the carbonaceous material is very fast, even when the ambient oxygen concentration is high, the rate of oxygen consumption at the surface due to the burning of the carbonaceous material is greater than the rate of oxygen supply due to oxygen diffusion within the gas film, resulting in a decrease in the oxygen concentration within the gas film. This causes incomplete combustion of the carbonaceous material, resulting in increased carbon monoxide generation. Therefore, if the combustion rate is very fast, some of the combustion heat of the carbonaceous material is emitted outside the system as carbon monoxide, reducing the reaction heat used for sintering and resulting in a decrease in yield. Here, by reducing the combustion rate of the carbonaceous material used and setting the combustion initiation temperature to 550°C or higher, it is possible to eliminate the diffusion rate limitation within the gas boundary film in the oxygen supply during the combustion reaction and to suppress the emission of part of the combustion heat to the outside of the system as carbon monoxide.

炭材の燃焼速度は、炭材の単位面積当たりの燃焼速度定数の低下、表面積の低下などによって影響を受けると考えられるが、燃焼速度定数は炭材の性状によって決まる値であり制御は困難である。表面積の低下には炭材の粒径の増加、あるいは表面をコーティングするなどの方法がある。しかし、粒径については既存プロセスでは使用が難しい大きさまで上昇させる必要があること、コーティングに関しては粉体のコーティングは技術的に難しく、目標とする表面積への制御が困難である。 The combustion rate of carbonaceous materials is thought to be affected by a decrease in the combustion rate constant per unit area of the carbonaceous material and a decrease in surface area, but the combustion rate constant is a value determined by the properties of the carbonaceous material and is difficult to control. Methods for decreasing surface area include increasing the particle size of the carbonaceous material or coating the surface. However, the particle size needs to be increased to a size that is difficult to use with existing processes, and coating powder is technically difficult, making it difficult to control the surface area to the target level.

以上のことから、燃焼速度の大きい炭材使用時には燃焼速度が低い炭材を混合し、総合的に燃焼速度を制御することが現実的である。そのため、本発明では、特にバイオマス炭等の化石燃料以外の燃焼開始温度が550℃未満の炭材を使用する際、燃焼開始温度が高い炭材を添加して配合し、配合した炭材の燃焼開始温度の加重平均を550℃以上とする。これにより、焼結鉱の歩留低下を抑制しつつ、カーボンニュートラルの考え方から、系外へのCO排出量を抑制することができる。 For these reasons, it is practical to use a carbonaceous material with a high combustion rate by mixing it with a carbonaceous material with a low combustion rate to comprehensively control the combustion rate. Therefore, in the present invention, when using a carbonaceous material other than fossil fuels, such as biomass charcoal, whose combustion initiation temperature is less than 550°C, a carbonaceous material with a high combustion initiation temperature is added and blended to make the weighted average of the combustion initiation temperatures of the blended carbonaceous materials 550°C or higher. This makes it possible to suppress a decrease in sinter yield while suppressing CO2 emissions outside the system from the perspective of carbon neutrality.

また、好適な実施態様として、少なくとも2種類以上の炭材を配合済みの炭材の全量を、造粒工程の前に添加することが好ましい。これにより、配合炭材の偏析を抑制し、焼結造粒原料内に配合された炭材燃焼開始温度のばらつきを低減することができ、結果として焼結鉱の歩留のばらつきを抑制することができる。 In a preferred embodiment, the entire amount of the blended carbonaceous material containing at least two or more types of carbonaceous material is added before the granulation process. This suppresses segregation of the blended carbonaceous material and reduces the variation in the combustion start temperature of the carbonaceous material blended in the sintered granulated raw material, thereby suppressing the variation in sintered ore yield.

なお、燃焼開始温度が550℃未満の炭材としては、化石燃料を除く有機系資源、あるいは前記有機系資源を原料として製造されたもの、より具体的には、バイオマス炭、無煙炭、廃プラスチック炭、褐炭や亜瀝青炭を原料とするコークスを、好適に用いることができる。 As carbonaceous materials with a combustion initiation temperature of less than 550°C, organic resources other than fossil fuels, or materials produced using the above organic resources as raw materials, more specifically, coke made from biomass coal, anthracite, waste plastic coal, lignite, or subbituminous coal, can be suitably used.

<実施例1>
バッチ式の焼結試験装置を使用し、燃焼開始温度の異なる炭材を少なくとも2種類以上配合したものを用いて、投入熱量を揃えた条件で焼結して焼結鉱を製造した。炭材としては、一般的に使用されている粉コークス、無煙炭、その他燃焼開始温度が550℃未満のバイオマス炭、褐炭を使用した。上記炭材を単独で用いた例を参考例1-4とし、上記炭材を少なくとも2種類以上配合し、その燃焼開始温度の加重平均が550℃未満の例を比較例1-3とし、上記炭材を少なくとも2種類以上配合し、その燃焼開始温度の加重平均が550℃以上の例を実施例1-6とした。この時、炭材以外の原料配合は一定とした。そして、各例の炭材を使用して製造した焼結鉱の歩留を、焼結後の全試料を2mの高さから4回落下させた際の5mm以上の比率として求めた。結果を表1に示すとともに、その結果から成品歩留と燃焼開始温度の加重平均との関係を図2に示した。
Example 1
Using a batch-type sintering test apparatus, sintered ore was produced using a blend of at least two or more carbonaceous materials with different combustion initiation temperatures, sintering them under the same input heat. Commonly used carbonaceous materials were coke breeze, anthracite, and other biomass charcoal and lignite with combustion initiation temperatures below 550°C. Reference Examples 1-4 were used as examples using the carbonaceous materials alone. Comparative Examples 1-3 were used as examples using at least two or more of the carbonaceous materials, with a weighted average combustion initiation temperature below 550°C. Examples 1-6 were used as examples using at least two or more of the carbonaceous materials, with a weighted average combustion initiation temperature above 550°C. The blending of raw materials other than the carbonaceous materials was kept constant. The yield of sintered ore produced using each carbonaceous material was calculated as the percentage of particles 5 mm or larger when all sintered samples were dropped four times from a height of 2 m. The results are shown in Table 1, and the relationship between product yield and weighted average combustion initiation temperature is shown in Figure 2.

ここで、燃焼開始温度とは以下の手法で求めた。対象となる炭材を10mg計り取り、示差熱分析機能を有した電気炉において空気を200ml/minで流通しながら10℃/minで加熱する。燃焼開始温度に達すると炭材は燃焼を開始し、急激に発熱する。この時、時間を横軸にとり、示差熱分析における熱変化を縦軸にとり、その時間と熱変化の関係線を描く。示差熱分析において急激な発熱を検知する直前の熱変化の線の延長と検知した直後の熱変化の線の延長との交点を燃焼開始温度とした。 Here, the combustion initiation temperature was determined using the following method. 10 mg of the target carbonaceous material was weighed out and heated at 10°C/min in an electric furnace equipped with differential thermal analysis functions while air was circulated at 200 ml/min. When the combustion initiation temperature was reached, the carbonaceous material began to burn and rapidly generated heat. At this time, time was plotted on the horizontal axis and the heat change in the differential thermal analysis on the vertical axis, and a line representing the relationship between time and heat change was drawn. The combustion initiation temperature was determined as the intersection of the extension of the line representing the heat change just before the sudden heat generation was detected in the differential thermal analysis and the extension of the line representing the heat change just after the detection.

表1および図2の結果から、配合後の燃焼開始温度の加重平均の増加に伴い成品歩留が上昇することがわかった。また、配合後の燃焼開始温度の加重平均が550℃未満の比較例1-3では成品歩留は低い値となることがわかった。一方、少なくとも2種類の炭材配合後の燃焼開始温度の加重平均が550℃以上の実施例1-6では、成品歩留は比較例1-3より高く、550℃付近から成品歩留の上昇幅は飽和することがわかった。さらに、燃焼開始温度が550℃未満のバイオマス炭および褐炭では、単独で使用した場合(参考例1、参考例2)、成品歩留は低い値となった。しかし、それらを他の炭材と混合し燃焼開始温度の加重平均を550℃以上とすることで(実施例1-6)、成品歩留が高くなることがわかった。以上のことから、単独では成品歩留が低く使用することができない焼結開始温度が550℃未満の炭材でも、他の炭材とともに配合して焼結開始温度の加重平均を550℃以上とすることで、炭材として使用できることがわかった。 The results in Table 1 and Figure 2 show that product yield increases as the weighted average of the combustion initiation temperature after blending increases. Furthermore, it was found that in Comparative Example 1-3, where the weighted average of the combustion initiation temperature after blending was less than 550°C, the product yield was low. On the other hand, in Example 1-6, where the weighted average of the combustion initiation temperature after blending at least two types of carbonaceous materials was 550°C or higher, the product yield was higher than in Comparative Example 1-3, and it was found that the increase in product yield saturates around 550°C. Furthermore, when biomass charcoal and lignite, which have combustion initiation temperatures less than 550°C, were used alone (Reference Example 1, Reference Example 2), the product yield was low. However, it was found that by mixing them with other carbonaceous materials and setting the weighted average of the combustion initiation temperature to 550°C or higher (Example 1-6), the product yield increased. From the above, it was found that even carbonaceous materials with a sintering start temperature of less than 550°C, which cannot be used alone due to low product yield, can be used as carbonaceous materials by blending them with other carbonaceous materials to make the weighted average sintering start temperature 550°C or higher.

<実施例2>
表1における実施例1の条件で配合した炭材を、造粒工程前で添加する水準および造粒工程の後半で添加する水準を、それぞれ複数回実施し、成品歩留のバラツキを調査した。結果を図3に示す。その結果、造粒前に炭材を添加した水準では、成品歩留には8%程度のバラツキがあり、その平均値は87%であった。一方、造粒後半に炭材を添加した水準では、17%程度のバラツキがあり、85%を超える水準も存在したが、平均として造粒前に炭材を添加した水準よりも低い値となった。以上のことから、配合後の炭材の全量が造粒工程の前に添加されることが、好ましい態様となることがわかった。
Example 2
The carbonaceous material blended under the conditions of Example 1 in Table 1 was added multiple times before the granulation process and in the latter half of the granulation process, and the variability in product yield was investigated. The results are shown in Figure 3. As a result, in the level where the carbonaceous material was added before granulation, there was a variability of about 8% in product yield, with an average value of 87%. On the other hand, in the level where the carbonaceous material was added in the latter half of granulation, there was a variability of about 17%, with some levels exceeding 85%, but on average the value was lower than in the level where the carbonaceous material was added before granulation. From the above, it was found that it is a preferable embodiment for the entire amount of carbonaceous material after blending to be added before the granulation process.

本発明の焼結鉱の製造方法によれば、所定の炭材を用いることで、燃焼開始温度の低い炭材使用時の歩留低下を防止することができ、産業上有用である。 According to the sintered ore manufacturing method of the present invention, by using a specified carbonaceous material, it is possible to prevent a decrease in yield when using carbonaceous material with a low combustion start temperature, making it industrially useful.

1 焼結鉱の製造設備
2 ドラムミキサー
3 焼結機
4 破砕機
5 クーラー
6 篩分装置
11 原料供給装置
12 パレット台車
13 点火炉
14 ウインドボックス
REFERENCE SIGNS LIST 1 sintered ore manufacturing equipment 2 drum mixer 3 sintering machine 4 crusher 5 cooler 6 sieving device 11 raw material supply device 12 pallet cart 13 ignition furnace 14 wind box

Claims (4)

固体燃料としての炭材を含む焼結配合原料を造粒して焼結用造粒原料を作製し、その焼結用造粒原料を焼結して焼結鉱を得る焼結鉱の製造方法において、前記炭材として、少なくとも2種類以上の炭材を配合した炭材であって、その燃焼開始温度の加重平均が550℃以上であるものを用いて焼結するとともに、配合後の炭材の全量が造粒工程の前に添加されることを特徴とする、焼結鉱の製造方法。 A method for producing sintered ore, which comprises granulating a blended sintering raw material containing a carbonaceous material as a solid fuel to produce a granulated raw material for sintering, and sintering the granulated raw material for sintering to obtain sintered ore, characterized in that the carbonaceous material is a blend of at least two types of carbonaceous material, the weighted average of whose combustion start temperatures is 550°C or higher , and the entire amount of the blended carbonaceous material is added before the granulation step . 前記配合する炭材に燃焼開始温度が550℃未満のものが含まれていることを特徴とする、請求項1に記載の焼結鉱の製造方法。 The method for producing sintered ore described in claim 1, characterized in that the blended carbonaceous material includes one with a combustion start temperature of less than 550°C. 前記燃焼開始温度が550℃未満の炭材が、化石燃料を除く有機系資源、あるいは前記有機系資源を原料として製造されたものを含むことを特徴とする、請求項2に記載の焼結鉱の製造方法。 The method for producing sintered ore described in claim 2, characterized in that the carbonaceous material having a combustion initiation temperature of less than 550°C includes organic resources other than fossil fuels, or materials produced using such organic resources as raw materials. 前記燃焼開始温度が550℃未満の炭材が、バイオマス炭、無煙炭、廃プラスチック炭、褐炭や亜瀝青炭を原料とするコークスであることを特徴とする、請求項3に記載の焼結鉱の製造方法。 The method for producing sintered ore described in claim 3, characterized in that the carbonaceous material having a combustion start temperature of less than 550°C is coke made from biomass coal, anthracite, waste plastic coal, lignite, or subbituminous coal.
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