JPH0136880B2 - - Google Patents
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- JPH0136880B2 JPH0136880B2 JP18995283A JP18995283A JPH0136880B2 JP H0136880 B2 JPH0136880 B2 JP H0136880B2 JP 18995283 A JP18995283 A JP 18995283A JP 18995283 A JP18995283 A JP 18995283A JP H0136880 B2 JPH0136880 B2 JP H0136880B2
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- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
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- Solid Fuels And Fuel-Associated Substances (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
(産業上の利用分野)
本発明は、転炉で鋼を精錬する際の溶銑温度を
上昇せしめることを目的とする製鋼炉用コークス
団鉱の製造方法に関するものである。
(発明が解決しようとする課題)
従来、一貫製鉄所においては、約1350℃の高炉
溶銑を転炉(以下製鉄炉の例として転炉について
述べる)で石炭、蛍石、マンガン鉱石、合金鉄等
の副原料を添加して酸素ガスを吹き込み、溶銑の
硅素、燐、炭素等の不純物を除いて鋼としていた
が、かかる精錬に於ては、脱硅時等の酸化発熱反
応で炉内温度が上がるため、予め鉄鉱石或は製鉄
後の加工工程で発生する鋼の切断屑等の屑鉄を装
入しておいて、その溶解或いは反応での吸熱を利
用して最適温度が維持されていた。従つて製鉄所
全体としての鉄の歩留が良く、又溶銑不足等にお
いては転炉で出鋼量を増すことも容易であつた。
しかし、最近の最適製鉄法では、前述の炉での
脱硅、脱燐を炉外で酸化鉄及び石灰等を不活性ガ
スと共に吹き込みスラグの発生量を押え、かつ転
炉精錬時間の短縮による増産をねらいとした炉外
脱硅脱燐法が実施されるようになり、然るとき
は、吹込材の溶解吸熱、及び不活性ガスの持ち去
る顕熱等で溶銑温度が約100℃下り、従つて転炉
内精錬では、前記鉄鉱石或いは屑鉄の装入量が制
約されることとなり、製鉄所内での総合鉄の歩留
低下及び製鉄所内における屑鉄在庫の増加、或い
は溶銑不足時への対応が不可能であるなどの問題
があつた。
一方、本発明で云う強粘結炭コークス材(以下
コークス粉という)は、高炉使用を主目的とし強
粘結炭を乾留して作られた硬いコークスを、破
砕、篩分して篩上を高炉へ供給し、篩下のコーク
ス粉は発生量に較べ用途が少くかつ嵩比重が小さ
いため、在庫量の逐次増加で広い貯蔵場を必要と
し、環境面から風による飛散防止対策等の貯蔵場
管理に苦慮していた。尚、前記コークス粉を転炉
で溶銑温度の昇温用として用いたが、転炉装入前
のホツパーで棚かけによる供給不足を起し易く、
又炉内においては、炉内上昇流による飛散損失等
で50%程度の熱効率となり、エネルギー損失が多
く、従つてコークス粉の塊化が要望されるに至つ
た。
又、本発明で用いる製鋼スラグ粉は、例えば転
炉精錬において発生する製鋼スラグを、有効利用
の見地から破砕、篩分或いは磁選等を行なつて、
鉄を回収し、スラグは路盤材、骨材等に利用され
るようになつたが、その各工程で発生する粉じん
は環境対策のため集じん機を設けて粉じんを回収
している。この回収された粉じんは、粒径が0.15
mm(100メツシユ)以下でかつ平均粒径が0.03mm
の乾燥微粉状であるため現在利用法がなく、専ら
粉じんの飛散を起さないような措置を施こして投
棄されている。
(課題を解決するための手段)
本発明は、上述問題点及び要望等に応えんとす
る転炉内昇温用に用いることを主目的とした製鋼
炉用コークス団鉱の製造方法を提供せんとするも
ので、その要旨は、
強粘結炭コークス粉の粘度構成を、3mm以下80
重量部以上と残部の20重量部以下が10〜3mm超と
なる如く整粒し、次に整粒したコークス粉乾燥重
量100部に対して製鋼スラグ粉を5〜20重量部と、
有機粘結剤を固形換算で0.15〜2重量部とを添加
し、尚該混合物の乾燥重量100部に対して水分を
6〜12重量部に調整して混合し、得られた混合物
を連続圧縮成形機で成形して通気養生せしめるこ
とを特徴とする製鋼炉用コークス団鉱の製造方法
である。
本発明について更に詳しく図面を参照して説明
する。
第1図は本発明の製造法を示す一実施例の工程
図である。予め含水率(乾燥重量100部に対する
水分の重量割合を示し、以下文中では単に重量部
と表示する。)を検知したコークス粉は、受入ホ
ツパー1及び下部のベルトフイーダー2によつて
定量に切出され、ベルトコンベヤー3で乾燥装置
付振動コンベヤー4へ送られて含水率を約8重量
部とすると共に5mm目の篩網で篩分け、篩上は篩
上産物箱5へ、篩下はベルトコンベヤー6を介し
てサブホツパー7で仮置し、間欠的にかつ定量的
に混合機8に供給する。一方製鋼スラグ粉と、有
機物粘結剤は、ホツパー7、フイダー10及びタ
ンク11、定量器12より夫々コークス粉の量に
応じて混合機8へ切出して、混合し、得られた混
合物を連続圧縮成形機13に供給して連続的にコ
ークス団鉱とする。成形されたコークス団鉱は下
部のネツトコンベヤー14で未成形物を篩分け、
ベルトコンベヤー15で成品箱16へ収納する。
ネツトコンベヤー14の篩下は、再びロール圧縮
成形機13へヒレ付コンベヤー17で送り返し、
前記混合物と共に圧縮成形される。18は熱風発
生装置、19は排気フアンである。尚成品箱16
は下面がネツト状の通気性のもので成品置場20
でコークス団鉱は転炉装入用として適した強度を
有す迄通気養生される。
本発明の方法で、コークス粉を含水率約8重量
部迄乾燥するのは、コークスが多孔質であるため
コークス製造時の水冷或いは屋外貯蔵場での吸水
により、通常の含水率が13〜17重量部と高く、含
水率が高いと成形時水分により圧縮が緩和されて
弱い団鉱となり、又連続圧縮成形材のロール型枠
面での表面張力により団鉱を吸着して型ばなれを
悪くし成形不良を起し易く成形歩留を低下させる
要因となる。又成形直後の強度を維持するため有
機粘結剤を添加するが、過剰水分により粘結剤が
希釈されるため成形直後の粘結効果を阻害するな
どの欠点を解消するため本発明では水分調整を必
要とする。
本発明に於ける含水率の適正範囲は、転炉工場
の規模により団鉱の必要強度は異なる。例えば運
搬或いは装入での落差によつて強度が決定される
もので、その落下に耐える程度の強合でよい。従
つて成形時の圧縮力は概ね600Kg/cm2〜1600Kg/
cm2の範囲であれば通常使用に耐える団鉱となるの
で、この条件における成品の気孔率を全水分範囲
の基準とし、実施例においては、別に添加する粘
結剤の水分をも考慮して決定する。本発明で限定
する含水率6〜12重量部の範囲内であれば満足す
べき団鉱強度を得ることが出来る。又含水率が6
重量部以下となつた場合は、湿つたコークス粉を
添加して本発明の方法に従えばよい。
次に、振動コンベヤー4で5mmに篩分けるの
は、圧縮成形後の団鉱強度が前記含水率のほか原
料の粒度構成にも影響があり、顧客の団鉱強度に
応じて粒度構成を整えた例である。コークス粉は
置場で山積で貯蔵されているため、粒度分布は偏
析を起しており、従つて粗い粒子群の場合は圧縮
成形においては空隙率が高いため粒子間の接合力
が弱いため壊れ易いので、成形歩留が悪く又弱い
団鉱となり易い。従つて均一な強度を有する団鉱
を作るためには、篩分を行つて均一な最適粒度構
成としたもので、3mm以下のものがコークス粉
100重量部に対し80重量部を超えると3mm超〜10
mmのものがあつても粉の干渉作用で団鉱強度の影
響は少ない。尚粒径が10mmを超えると、圧縮成形
で上述要因で団鉱強度を弱くする原因ともなるの
で本発明では10mmを超えない大きさとする。
第3図は一実施例の振動コンベヤー4で回収し
た粒径5〜10mmの篩上コークスを篩下に混合し、
粒径3mm以下の分布を変化させて成形したときの
成形歩留と成形直後の圧潰強度との関係を示す図
である。本実験では、5mm以上の篩状コークスを
混合して本発明第1図のコンベヤー6より供給
し、コークス粉乾燥重量100重量部に対し、100メ
ツシユ以下の乾燥製鋼スラグ微粉を10重量部、及
びリグニン水溶液を乾燥固形分換算で2重量部相
当を添加混合して第1図の工程に従つて成形し、
ベルトコンベヤー15より排されるものを一定時
間全量採取して完全に成形を保つたものの重量割
合を歩留とし、又数個の圧潰強度を測定した結果
を第3図に示す。なお、前記成形前の含水率は約
9重量部であつた。なお、連続圧縮成形機13の
圧縮力は1000Kg/cm2で、団鉱の形状は厚さ21mm、
幅35mm、長さ46mmの豆炭状に成形した。
第3図のA区は成形歩留の区域、B区は圧潰強
度の区域を示す。第3図より成形直後の取扱いを
容易となるためには圧潰強度を3.5Kg以上確保す
る必要があり、従つてコークス粉100重量部に対
し粒径3mm以下の占める割合が80重量部以上必要
であることが判明した。尚、圧潰強度とは、本発
明のコークス団鉱が楕円形の球形からなる豆炭状
であるためその球面を押圧して団鉱の潰れるとき
の押圧荷重である。
又本発明で製鋼スラグ粉を添加混合するのは、
コークス粉が多孔質であり而もその面は細い非結
晶の球面の溶着群であるため、コークス粉のみで
は粒子間の接合力が弱く、圧縮成形には多量の強
力な接着力のある結合剤を必要とする欠点があ
る。従つて結晶質の製鋼スラグを加えてコークス
粒子面を取り囲み結晶質粒子を絡らませて圧縮成
形し、緻密な強い団鉱を成形するためである。因
みに、製鋼スラグ粉末添加のコークス団鉱の見掛
比重は1.26であるが、製鋼スラグ粉を添加するこ
とにより、見掛比重は1.54となり重くて強い団鉱
となる。又成形後の養生において団鉱中の水分の
影響で製鋼スラグ中の未さい化石灰及びカルシウ
ムシリケート等からライムの溶出或いは晶出、並
びに含有する鉄分からウースタイトの溶出がある
ため、これが団鉱中の微細な気孔に浸透して、更
に粒子間の接合に寄与するなど自硬効果を有する
利点がある。又転炉装入において、製鋼スラグは
転炉発生物であるため転炉精錬では成分的には無
害であり、団鉱としては製鋼スラグの軟化効果に
より急激な熱解裂を防止し、又団鉱の比重を重く
するため炉内での浮遊流動を防止することから熱
効率を高める効果がある。
従つて、上述団鉱の強度を高めるために用いる
製鋼スラグは比較的細いものが微細間隙への充填
性が良く、又養生中の自硬反応においても被表面
量の大きい小さい粒子が良いことから、粒子構成
としては、製鋼スラグ粉100重量部中100メツシユ
以下の占める割合が80重量部以上のものがその効
果は顕著である。又添加量は、コークスの被表面
を覆いかつ成形時の粒子空隙を埋める程度で良
く、多量の添加は徒らに粒子群の被表面積を増加
させるため、成形直後の強度を維持するために添
加する有機粘結剤の効果を妨げる要因ともなるの
で、実施例ではコークス粉100重量部に対し5〜
20重量部の範囲の添加においてその目的を得るこ
とが出来た。すなわち、製鋼スラグのコークス分
に対する添加を20重量部以上とすると団鉱のカロ
リーが落ち、又5重量部以下であると結合力が弱
くなる。
有機粘結剤の添加は、上述製鋼スラグ粉のみで
は成形直後で圧縮破壊には強いが脆い欠点を補
い、成形後の取扱での落下に耐える程度の量を添
加する。従つて粘結剤は、即効性で接着力があ
り、而も転炉精錬に無害な成分を有するものが望
まれるため、炭素、水素、酸素を主成分とした有
機物高分子系例えば、リグニンを主成分とするも
のや糖蜜(これらのものは水溶液100重量部に対
し固形分が通常20〜50重量部の濃縮液である)、
或いはポリビニールアルコールなどの高分子樹脂
等がよい。尚有機物であるため、発熱量を有する
ことから団鉱の熱量に寄与することが出来る。添
加量は上述の如く、成形直後の取扱に耐える量で
よく、添加する物質の接着力によつて異る。例え
ば、実施例ではコークス粉100重量部に対しリグ
ニン水溶液を4重量部(固形では2重量部)添加
して成形直後満足すべき強度を得ることが出来
た。輸送中の破壊、経済性、粘結性を発揮する最
少値を考慮してコークス100重量部に対し有機物
粘結剤0.3〜4重量部(固形換算0.15〜2重量部)
の範囲でよい。
第2図は、コークス粉の全量を成形する他の実
施例の製造工程を示すもので、前記実施例の振動
コンベヤー4と混合機8を乾燥機21及びフレツ
トミル22に置き替え、コークス粉を乾燥後フレ
ツトミル22で3mm以下の粒子コークス粉100重
量部に対し80重量部以上となる迄で粉砕しながら
製鋼スラグを混合し、粘結剤を加えて成形したも
ので団鉱の強度は前記実施例と殆んど変わりな
い。従つて、コークス粉の整粒は分級或いは粉砕
何れの方法でもよい。
本発明の方法で製造したコークス団鉱の、成形
直後の落下強度は鉄板上へ1〜2mより1回の落
下で耐えられる程度であつたが、7日間成品箱1
6に500mmの深さに収納し、湿度50〜70%の屋内
で自然通気養生を行うと製鋼スラグ粉の水分との
反応での自硬効果と有機粘結剤の効果により第4
図に示すように強い団鉱となつた。
第4図は、第1図の工程によつて第1表No.3に
示す配合で混合し、連続圧縮成形機13の圧縮力
を1000Kg/cm2で成形した本発明のコークス団鉱を
製品箱16に収納して成品置場20で通気養生中
その経過時毎の落下強度を示す図である。落下強
度はコークス団鉱1Kgを袋に入れ10mの高さより
鉄板上へ3回繰返し落下させた後、5mm網目の篩
で篩分けた篩上の重量歩留で示す。第4図の横軸
に養生経過日数を示し、縦軸には上述測定の5mm
網目の重量歩留を示すもので、養生日数の経過に
より5mm以上の歩留が多くなり7日でほぼ通常の
大型転炉の使用に耐える団鉱となる。従つて製鋼
スラグの自硬効果の反応成生期間及び反応熱或い
は通気での乾燥期間が7日間に至ると考えられ
る。
団鉱の大きさとしては、大きくなれば自重によ
る落下衝撃で壊れ易く、又転炉内で短時間で昇温
する目的に使えない、例えば製錬途中で昇温を必
要とする場合は5〜7分程度の短時間での燃焼が
要求され、燃え残りを生じるとエネルギー損失と
もなり、小さければ取扱いにおいて壊れて5mm以
下となり転炉内で飛散し易い欠点があるため、大
きさとしては、巾、長さ及び厚さが10〜50mmの範
囲が好ましい。又形状は角のない球面が落下衝撃
に対して強いので通常の楕円形の豆炭状のものが
良い。
実施例のコークス団鉱の形状は、巾35mm、長さ
46mm、厚さ21mmの寸法で各稜線及びコーナーを球
形状とした豆炭状のものである。
(実施例)
以下実施例を第1表に示す。
(Industrial Application Field) The present invention relates to a method for producing coke briquette for a steelmaking furnace, the purpose of which is to increase the temperature of hot metal when refining steel in a converter. (Problem to be solved by the invention) Conventionally, in an integrated steelworks, blast furnace molten pig iron at about 1350℃ is processed into coal, fluorite, manganese ore, ferroalloy, etc. in a converter (hereinafter, a converter will be described as an example of a steelmaking furnace). In this refining process, impurities such as silicon, phosphorus, and carbon are removed from the hot metal by blowing oxygen gas into it, but during such refining, the temperature inside the furnace rises due to oxidative exothermic reactions such as during desiliconization. To avoid this, the optimum temperature was maintained by charging scrap iron such as iron ore or steel cutting scraps generated in the processing process after steel manufacturing, and utilizing the heat absorbed by the melting or reaction. Therefore, the yield of iron for the steelworks as a whole was good, and it was easy to increase the amount of steel produced in the converter when there was a shortage of hot metal. However, in the latest optimal steelmaking method, the above-mentioned desiliconization and dephosphorization in the furnace are performed outside the furnace by blowing iron oxide, lime, etc. together with an inert gas to suppress the amount of slag generated, and increase production by shortening the converter refining time. Ex-furnace desiliconization and phosphorization methods have been implemented with the aim of In refining in a converter, the amount of iron ore or scrap iron charged is limited, resulting in a decrease in the overall iron yield within the steelworks, an increase in scrap iron inventory within the steelworks, or an inability to respond to hot metal shortages. There were some questions about whether it was possible. On the other hand, the strong coking coal coke material (hereinafter referred to as coke powder) referred to in the present invention is made by crushing and sifting hard coke made by carbonizing strong coking coal mainly for use in blast furnaces. The coke powder under the sieve that is supplied to the blast furnace has few uses compared to the amount generated and has a small bulk specific gravity, so as the amount of inventory increases gradually, a large storage area is required. It was difficult to manage. Although the coke powder was used to raise the temperature of hot metal in a converter, it is easy to run out of supply due to shelving in the hopper before charging into the converter.
Furthermore, in the furnace, the thermal efficiency is about 50% due to scattering loss due to upward flow in the furnace, resulting in a large energy loss, and therefore, it has become necessary to agglomerate the coke powder. In addition, the steelmaking slag powder used in the present invention is produced by crushing, sieving, magnetic separation, etc., steelmaking slag generated in converter refining, for example, from the viewpoint of effective utilization.
Iron is recovered and the slag is used for roadbed material, aggregate, etc., and dust collectors are installed to collect the dust generated in each process as an environmental measure. This collected dust has a particle size of 0.15
mm (100 mesh) or less with an average particle size of 0.03mm
Because it is in the form of a dry, fine powder, there is currently no use for it, and it is being dumped after taking measures to prevent it from scattering. (Means for Solving the Problems) The present invention provides a method for producing coke briquettes for steelmaking furnaces, which is primarily intended for use in increasing temperature in converters, in order to meet the above-mentioned problems and demands. The gist is that the viscosity composition of strongly coking coal coke powder should be 3 mm or less80
The coke powder is sized so that more than 20 parts by weight and the remaining part is less than 20 parts by weight exceeds 10 to 3 mm, and then 5 to 20 parts by weight of steelmaking slag powder is added to 100 parts by weight of the sized coke powder dry weight,
Add 0.15 to 2 parts by weight of an organic binder on a solid basis, adjust the water content to 6 to 12 parts by weight based on 100 parts of the dry weight of the mixture, and mix.The resulting mixture is subjected to continuous compression. This is a method for producing coke briquette for steelmaking furnaces, which is characterized by forming it with a forming machine and aerating it. The present invention will be explained in more detail with reference to the drawings. FIG. 1 is a process diagram of an embodiment showing the manufacturing method of the present invention. The coke powder whose moisture content has been detected in advance (indicates the weight ratio of moisture to 100 parts of dry weight, hereinafter referred to simply as parts by weight) is cut into fixed quantities by the receiving hopper 1 and the lower belt feeder 2. It is sent to a vibrating conveyor 4 with a drying device by a belt conveyor 3, and the moisture content is reduced to about 8 parts by weight, and it is sieved through a 5 mm sieve screen. It is temporarily placed in a sub-hopper 7 via a conveyor 6, and is intermittently and quantitatively supplied to a mixer 8. On the other hand, the steelmaking slag powder and the organic binder are cut out from the hopper 7, feeder 10, tank 11, and quantitative meter 12 into the mixer 8 according to the amount of coke powder, and mixed, and the resulting mixture is continuously compressed. It is supplied to a molding machine 13 to continuously form coke briquettes. The formed coke briquette is passed through a net conveyor 14 at the bottom, where unformed materials are sieved.
The products are stored in a finished product box 16 by a belt conveyor 15.
The unsieved material of the net conveyor 14 is sent back to the roll compression molding machine 13 by the fin conveyor 17, and
Compression molding is carried out together with the mixture. 18 is a hot air generator, and 19 is an exhaust fan. Shosei product box 16
is a breathable material with a net-like bottom surface.
The coke briquette is then aerated and cured until it has a strength suitable for charging into a converter. In the method of the present invention, coke powder is dried to a water content of about 8 parts by weight because coke is porous, and the water content is normally reduced to 13 to 17 parts by water cooling during coke production or by water absorption in an outdoor storage area. If the weight part is high and the moisture content is high, the compression will be relaxed due to moisture during molding, resulting in weak briquettes, and the surface tension on the roll form surface of the continuous compression molded material will adsorb the briquettes, making mold deformation worse. This tends to cause molding defects, which is a factor that reduces molding yield. In addition, an organic binder is added to maintain the strength immediately after molding, but in order to overcome the drawbacks such as inhibiting the caking effect immediately after molding because the binder is diluted by excess water, moisture adjustment is used in the present invention. Requires. The appropriate range of moisture content in the present invention varies depending on the scale of the converter factory and the required strength of the briquette. For example, the strength is determined by the drop during transportation or charging, and it may be strong enough to withstand the drop. Therefore, the compression force during molding is approximately 600Kg/cm 2 ~1600Kg/
If it is in the cm 2 range, the briquette can be used normally, so the porosity of the product under this condition is used as the standard for the entire moisture range, and in the examples, the moisture of the binder added separately is also taken into account. decide. Satisfactory briquette strength can be obtained if the water content is within the range of 6 to 12 parts by weight as defined in the present invention. Also, the moisture content is 6
If the amount is less than parts by weight, wet coke powder may be added and the method of the present invention may be followed. Next, the reason why the briquette is sieved into 5 mm pieces using the vibrating conveyor 4 is that the strength of the briquette after compression molding is affected not only by the moisture content but also by the particle size structure of the raw material, so the particle size structure is adjusted according to the customer's briquette strength. This is an example. Because coke powder is stored in piles at storage sites, the particle size distribution is segregated, and coarse particles tend to break during compression molding due to the high porosity and weak bonding force between particles. Therefore, the molding yield is poor and the briquette tends to be weak. Therefore, in order to make briquettes with uniform strength, it is necessary to sieve to obtain a uniform and optimal particle size composition, and particles of 3 mm or less are considered coke powder.
If it exceeds 80 parts by weight per 100 parts by weight, it exceeds 3 mm ~ 10
Even if there are mm ones, the influence of the briquette strength is small due to the interference effect of the powder. If the particle size exceeds 10 mm, the strength of the briquette may be weakened due to the above-mentioned factors during compression molding, so in the present invention, the particle size is set not to exceed 10 mm. FIG. 3 shows that coke on the sieve with a particle size of 5 to 10 mm collected by the vibrating conveyor 4 of one embodiment is mixed in the bottom of the sieve.
FIG. 3 is a diagram showing the relationship between the molding yield and the crushing strength immediately after molding when molding is performed by changing the distribution of particle sizes of 3 mm or less. In this experiment, sieved coke of 5 mm or more was mixed and supplied from the conveyor 6 shown in Fig. 1 of the present invention, and 10 parts by weight of dry steel slag fine powder of 100 mesh or less was added to 100 parts by weight of dry coke powder, and Add and mix an aqueous lignin solution equivalent to 2 parts by weight in terms of dry solid content, and mold according to the process shown in Figure 1.
The weight percentage of the products that were completely kept in shape by collecting all the products discharged from the belt conveyor 15 for a certain period of time was taken as the yield, and the results of measuring the crushing strength of several products are shown in FIG. Note that the water content before the molding was about 9 parts by weight. The compression force of the continuous compression molding machine 13 is 1000Kg/ cm2 , and the shape of the briquette is 21mm thick.
It was formed into a charcoal shape with a width of 35 mm and a length of 46 mm. In FIG. 3, section A indicates the area of molding yield, and section B indicates the area of crushing strength. Figure 3 shows that in order to facilitate handling immediately after molding, it is necessary to ensure a crushing strength of 3.5 kg or more, and therefore the ratio of particles with a diameter of 3 mm or less to 100 parts by weight of coke powder must be 80 parts by weight or more. It turns out that there is something. Note that the crushing strength is the pressing load when the briquette is crushed by pressing the spherical surface, since the coke briquette of the present invention is in the form of an elliptical sphere. In addition, in the present invention, steelmaking slag powder is added and mixed by:
Since coke powder is porous and its surfaces are welded groups of thin amorphous spheres, coke powder alone has a weak bonding force between particles, and compression molding requires a large amount of a binder with strong adhesive force. There is a drawback that it requires Therefore, crystalline steelmaking slag is added to surround the coke particle surfaces, entangle the crystalline particles, and perform compression molding to form a dense and strong briquette. Incidentally, the apparent specific gravity of coke briquette with steelmaking slag powder added is 1.26, but by adding steelmaking slag powder, the apparent specific gravity becomes 1.54, resulting in a heavy and strong briquette. In addition, during curing after forming, due to the influence of moisture in the briquette, lime is leached or crystallized from unsalted lime and calcium silicate in the steelmaking slag, and wustite is leached from the iron contained in the steelmaking slag. It has the advantage of having a self-hardening effect, such as penetrating into the fine pores of the particles and contributing to bonding between particles. In addition, in charging the converter, steelmaking slag is a product of the converter, so it is harmless in terms of components during converter refining, and as a briquette, the softening effect of steelmaking slag prevents rapid thermal decomposition, and the briquette This has the effect of increasing thermal efficiency by increasing the specific gravity of the ore and preventing floating flow within the furnace. Therefore, the relatively thin steelmaking slag used to increase the strength of the briquettes described above has a good ability to fill minute gaps, and small particles with a large surface coverage are also good for the self-hardening reaction during curing. As for the particle composition, the effect is remarkable when the proportion of 100 mesh or less in 100 parts by weight of steelmaking slag powder is 80 parts by weight or more. Also, the amount added should be enough to cover the coke surface and fill the particle voids during molding. Adding a large amount will unnecessarily increase the surface area of the particles, so it is necessary to add it to maintain strength immediately after molding. This can be a factor that hinders the effect of organic binders, so in the examples, 5 to 5 parts by weight of coke powder is used.
The objective could be achieved at additions in the range of 20 parts by weight. That is, if the amount of steelmaking slag added to the coke content is 20 parts by weight or more, the calorie content of the briquette decreases, and if it is less than 5 parts by weight, the binding strength becomes weak. The organic binder is added in an amount sufficient to compensate for the drawback that the above-mentioned steelmaking slag powder alone is strong against compressive fracture but brittle immediately after molding, and to withstand falling during handling after molding. Therefore, it is desirable that the binder be fast-acting, adhesive, and contain components that are harmless to converter refining. or molasses as the main ingredient (these are concentrated liquids with a solid content of usually 20 to 50 parts by weight per 100 parts by weight of an aqueous solution),
Alternatively, a polymer resin such as polyvinyl alcohol may be used. Since it is an organic substance, it has a calorific value and can contribute to the calorific value of the briquette. As mentioned above, the amount added may be an amount that can withstand handling immediately after molding, and will vary depending on the adhesive strength of the added substance. For example, in the example, by adding 4 parts by weight of an aqueous lignin solution (2 parts by weight in solid form) to 100 parts by weight of coke powder, satisfactory strength could be obtained immediately after molding. Considering the minimum value for destruction during transportation, economic efficiency, and caking properties, add 0.3 to 4 parts by weight of organic binder to 100 parts by weight of coke (0.15 to 2 parts by weight in terms of solids).
The range is fine. FIG. 2 shows the manufacturing process of another embodiment in which the entire amount of coke powder is molded. The briquette was then milled using a fret mill 22 until it became 80 parts by weight or more per 100 parts by weight of coke powder with particles of 3 mm or less in size, mixed with steelmaking slag, added with a binder, and molded. There is almost no difference. Therefore, coke powder may be sized by either classification or pulverization. The drop strength of the coke briquette produced by the method of the present invention immediately after forming was such that it could withstand a single drop from 1 to 2 m onto a steel plate,
When the steelmaking slag powder is stored at a depth of 500 mm and cured with natural ventilation indoors at a humidity of 50 to 70%, the self-hardening effect due to the reaction of the steelmaking slag powder with moisture and the effect of the organic binder will cause the
As shown in the figure, it became a strong briquette. Figure 4 shows a product of the coke briquette of the present invention, which is mixed with the composition shown in Table 1 No. 3 according to the process shown in Figure 1 and molded with a compression force of 1000 kg/cm 2 in a continuous compression molding machine 13. FIG. 4 is a diagram showing the fall strength at each time point during aeration and curing in the product storage area 20 after being stored in a box 16. Drop strength is measured by placing 1 kg of coke briquette in a bag and repeatedly dropping it from a height of 10 m onto an iron plate three times, and then sieving through a 5 mm mesh sieve. The horizontal axis of Figure 4 shows the number of days elapsed after curing, and the vertical axis shows the 5mm
This shows the weight yield of the mesh, and as the number of curing days passes, the yield of 5 mm or more increases, and in 7 days it becomes a briquette that can withstand the use of a normal large converter. Therefore, it is thought that the reaction formation period of the steelmaking slag's self-hardening effect and the drying period due to reaction heat or ventilation are up to 7 days. Regarding the size of the briquette, if it becomes large, it will easily break due to the impact of falling due to its own weight, and it cannot be used for the purpose of raising the temperature in a short time in the converter. Burning is required in a short time of about 7 minutes, and if there is any unburned remains, there is a loss of energy, and if it is small, it will break during handling and become less than 5 mm and will easily scatter in the converter. , the length and thickness are preferably in the range of 10 to 50 mm. Also, since a spherical surface with no corners is strong against drop impact, it is best to use a regular oval charcoal-like shape. The shape of the coke briquette in the example is 35 mm in width and length.
It is charcoal-like with dimensions of 46 mm and thickness of 21 mm, and each ridge line and corner are spherical. (Example) Examples are shown in Table 1 below.
【表】【table】
【表】
(発明の効果)
上述の如く、本発明の方法で製造したコークス
団鉱は、従来未利用であつた製鋼スラグ粉を加え
ることによつて、殆んど塊コークスと変わらない
効果を有するものとなり、熱エネルギーへの寄
与、及び製鋼歩留の向上或いは製鋼増産へも安価
に寄与できるものである。而も最近の新製鉄法に
於ては、特に要望される極めて有用なものであ
る。[Table] (Effects of the invention) As mentioned above, the coke briquette produced by the method of the present invention has almost the same effect as lump coke by adding steelmaking slag powder, which has been unused in the past. Therefore, it can contribute to thermal energy, improve steel manufacturing yield, or increase steel manufacturing production at low cost. However, it is extremely useful and in particular demand in recent new iron manufacturing methods.
第1図は本発明のコークス団鉱の製造工程図、
第2図は本発明の他の製造工程図、第3図は圧縮
成形前のコークスの粒度分布と成形歩留及び圧潰
強度を示す図、第4図は実施例の養生経過におけ
る落下強度を示す図である。
1;受入れホツパー、2;ベルトフイーダー、
3,6,13,15,17;ベルトコンベヤー、
4;振動コンベヤー、5;篩上産物箱、7;サブ
ホツパー、8;混合機、9;ホツパー、10;フ
イーダー、11;タンク、12;定量器、13;
ロール圧縮成形機、14;ネツトコンベヤー、1
6;成品箱、18;熱風発生装置、19;排気フ
アン、20;成品置場、21;乾燥機、22;フ
レツトミル、A;受入コークス粉の粒度構成範
囲、B;整粒後のコークス粉の粒度構成範囲、
C;成形歩留、D;圧潰強度。
FIG. 1 is a manufacturing process diagram of the coke briquette of the present invention,
Figure 2 is another manufacturing process diagram of the present invention, Figure 3 is a diagram showing the particle size distribution, molding yield, and crushing strength of coke before compression molding, and Figure 4 is a diagram showing the falling strength during the curing process of the example. It is a diagram. 1; Receiving hopper, 2; Belt feeder,
3, 6, 13, 15, 17; belt conveyor,
4; Vibration conveyor, 5; Screened product box, 7; Sub-hopper, 8; Mixer, 9; Hopper, 10; Feeder, 11; Tank, 12; Quantifier, 13;
Roll compression molding machine, 14; Net conveyor, 1
6; Product box, 18; Hot air generator, 19; Exhaust fan, 20; Product storage area, 21; Dryer, 22; Fret mill, A; Particle size composition range of received coke powder, B; Particle size of coke powder after sizing configuration range,
C: Molding yield, D: Crushing strength.
Claims (1)
80重量部以上と残部の20重量部以下が10〜3mm超
となる如く整粒し、次に整粒したコークス粉の乾
燥重量100部に対して製鋼スラグ粉を5〜20重量
部と、有機粘結剤を固形換算で0.15〜2重量部と
を添加し、尚該混合物の乾燥重量100部に対して
水分を6〜12重量部に調整して混合し、得られた
混合物を連続圧縮成形機で成形して通気養生せし
めることを特徴とする製鋼炉用コークス団鉱の製
造方法。1. The particle size structure of strongly coking coal coke powder is 3 mm or less.
The particles are sized so that 80 parts by weight or more and the remaining 20 parts by weight or less exceed 10 to 3 mm, and then 5 to 20 parts by weight of steelmaking slag powder are added to 100 parts by weight of the sized coke powder, and an organic Add 0.15 to 2 parts by weight of a binder on a solid basis, adjust the water content to 6 to 12 parts by weight based on 100 parts of the dry weight of the mixture, and mix.The resulting mixture is continuously compression molded. A method for producing coke briquette for steelmaking furnaces, which comprises forming the coke briquette in a machine and aerating it.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18995283A JPS6081294A (en) | 1983-10-13 | 1983-10-13 | Coke aggregates and manufacture thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18995283A JPS6081294A (en) | 1983-10-13 | 1983-10-13 | Coke aggregates and manufacture thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6081294A JPS6081294A (en) | 1985-05-09 |
| JPH0136880B2 true JPH0136880B2 (en) | 1989-08-02 |
Family
ID=16249939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18995283A Granted JPS6081294A (en) | 1983-10-13 | 1983-10-13 | Coke aggregates and manufacture thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6081294A (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100479998B1 (en) * | 1999-12-24 | 2005-03-30 | 주식회사 포스코 | method for manufacturing waste cokes from settling pond into heating material of molten pig iron |
| KR100905581B1 (en) * | 2001-12-21 | 2009-07-02 | 주식회사 포스코 | Coal Briquettes For Iron and Steel Making Process, Method Of Manufacturing Thereof |
| KR100687250B1 (en) | 2005-12-05 | 2007-02-27 | 주식회사 케이에스티 | Coke briquettes containing fractional ores and their preparation |
| CN103756701B (en) * | 2014-01-21 | 2015-11-25 | 河北联合大学 | Hyperergy coke and production method thereof |
| CN104232231B (en) * | 2014-09-18 | 2016-08-24 | 济南宝华新能源技术有限公司 | A kind of biomass-based fuel and preparation method |
| CN105238479A (en) * | 2015-10-14 | 2016-01-13 | 华北理工大学 | Steel slag checking tailing-modified biomass molded charcoal |
| CN105238474B (en) * | 2015-10-14 | 2018-07-17 | 华北理工大学 | The clean type coal and preparation method of additive are done using slag final election tailings |
| JP6869115B2 (en) * | 2017-06-12 | 2021-05-12 | 日鉄エンジニアリング株式会社 | How to make briquette for waste melting furnace and how to use briquette |
-
1983
- 1983-10-13 JP JP18995283A patent/JPS6081294A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6081294A (en) | 1985-05-09 |
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