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JPH0573707B2 - - Google Patents
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JPH0573707B2 - - Google Patents

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Publication number
JPH0573707B2
JPH0573707B2 JP19871484A JP19871484A JPH0573707B2 JP H0573707 B2 JPH0573707 B2 JP H0573707B2 JP 19871484 A JP19871484 A JP 19871484A JP 19871484 A JP19871484 A JP 19871484A JP H0573707 B2 JPH0573707 B2 JP H0573707B2
Authority
JP
Japan
Prior art keywords
pellets
weight
parts
cold
cement
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP19871484A
Other languages
Japanese (ja)
Other versions
JPS6177651A (en
Inventor
Hiroshi Isozaki
Kazuyuki Mizushima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP19871484A priority Critical patent/JPS6177651A/en
Publication of JPS6177651A publication Critical patent/JPS6177651A/en
Publication of JPH0573707B2 publication Critical patent/JPH0573707B2/ja
Granted legal-status Critical Current

Links

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  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明はコールドペレツト用急結剤、詳しくは
採掘の際発生する微粉鉄鉱石(以下粉鉱石とい
う)の処理方法の一つであるコールドペレツト用
急結剤に関する。 〔従来技術〕 近年鉄鉱石の使用量が急増し、優良鉄鉱石の埋
蔵量が減少したこと、選鉱技術の発達により品位
の高い粉鉱石が得られるようになつたことから、
ペレタイジング法は急激に数多く採用されるよう
になつた。粉鉱石のペレツトは適切な水分量で例
えばドラム型やパン型の造粒機を使用し、造粒後
焼成する焼成ペレツトが主流であつたが、省エネ
ルギーや環境対策等の見地から、焼成工程を省略
し、普通ポルトランドセメントをバインダーとす
るコールドペレツト法が行われている。 〔発明が解決しようとする問題点〕 通常、ペレツトの横持ちする際の最低強度(一
次ハンドリング強度)は約5〜20Kgf/cm2、高炉
に投入する時(二次ハンドリング強度)は約30〜
100Kgf/cm2が必要とされている。 しかしながら、普通ポルトランドセメントをバ
インダーとした場合は所定の強度が得られるまで
7〜14日の養生期間が必要であり、又ペレツトを
横持ちする間に粉化する場合が多い。 〔問題点を解決するための手段〕 本発明者らは、短時間にペレツトの強度を発現
させ、上記の問題点を解消すべく種々検討を重
ね、本発明を完成するに到つた。 即ち、本発明はカルシウムアルミネート、2価
の金属水酸化物及び1価の金属炭酸塩からなるコ
ールドペレツト用急結剤である。 以下本発明を詳細に説明する。 本発明で使用するカルシウムアルミネート(以
下CAという)としては3CaO・Al2O3,12CaO・
7Al2O3,CaO・Al2O3,CaO・2Al2O3及びCaO・
6Al2O3等の結晶質や非晶質が挙げられる。CA中
のCaO/Al2O3モル比が高いと急結性は強く、
CaO/Al2O3モル比が低いと急結性は弱くなる。
そのためCaO/Al2O3モル比は0.5〜4.0が好まし
く、1.0〜2.5が更に好ましい。 2価の金属水酸化物(以下M(OH)2という)
としては、水酸化カルシウム、水酸化マグネシウ
ム、水酸化鉄、水酸化亜鉛、水酸化マンガン等が
挙げられ、経済的に水酸化カルシウムが好まし
い。 M(OH)2の添加量はCA100重量部に対して10
〜200重量部が好ましく、50〜150重量部が更に好
ましい。 1価の金属炭酸塩(以下M2CO3という)とし
ては、炭酸ナトリウム、炭酸カリウム等が挙げら
れるが、経済性から炭酸ナトリウムが好ましい。 M2CO3の添加量はCA100重量部に対して10〜
100重量部が好ましく、20〜50重量部が更に好ま
しい。 本発明でCA,M(OH)2及びM2CO3を併用する
ことにしたのは、他のものでは高炉で実際に使用
するときに重要となる高温下におけるペレツトの
性状(以下高温性状という)が不良となる。即
ち、粉鉱石のペレツトは、良好な常温でのペレツ
トの性状及び高温性状が必要で、特に成分中にア
ルカリ分が多くなると高炉の損傷が大きく問題と
なる。コールドペレツト中のアルカリ分は約0.1
重量%以下とすることが好ましい。更にSO3等の
イオウ分や、塩素分はいずれも高炉に悪影響を及
ぼす。本発明はこれら有害成分を極力少なく抑え
たものである。 CA,M(OH)2及びM2CO3からなる急結剤はセ
メント等の水硬性物質と共に使用し、粉鉱石を造
粒し、コールドペレツトとする。 水硬性物質としては、普通ポルトランドセメン
ト、高炉セメント、フライアツシユセメント、シ
リカセメント、高炉水砕スラグ及び転炉スラグ等
が挙げられる。物性的には普通セメントが好まし
いが、経済性を考慮すれば産業副産物を利用した
ものが好ましく、高炉水砕スラグは更に好まし
い。 本発明の急結剤と水硬性物質の混合割合は、水
硬性物質100重量部に対し急結剤1〜20重量部が
好ましく、3〜10重量部が更に好ましい。 又、水硬性物質の添加量は、粉鉱石100重量部
に対して3〜15重量部が良く、5〜12重量部が更
に好ましい。水硬性物質の添加量がこれより少な
いと強度発現が悪く、多いと有効成分の含有率が
低下メリツトが減少する。 急結剤の各成分及び水硬性物質の添加方法は特
に限定されるものではなく、添加順序も特に規定
されるものではない。 混練物の作業性、及び、強度性状を改善するた
め、通常使用されるセメント減水剤、遅延剤及び
AE剤等のセメント混和剤を併用することができ
る。 又、1価の硫酸塩、アルミン酸塩、炭酸水素
塩、リン酸塩等も一部併用することもできる。 〔実施例〕 以下実施例で本発明を更に説明する。 実施例 1 表−1実験No.6〜15のように配合し、モルタル
ミキサー(JISR−5201)で3分間混練りした。
その後2×2×8cmの型枠に打設し、20℃気乾養
生を行つた。ハンドリングタイム及び圧縮強度を
測定した。結果を表−2に示す。
[Industrial Field of Application] The present invention relates to an accelerating agent for cold pellets, and more particularly to an accelerating agent for cold pellets, which is one of the methods for processing fine iron ore (hereinafter referred to as fine ore) generated during mining. . [Prior art] In recent years, the amount of iron ore used has increased rapidly, the reserves of high-quality iron ore have decreased, and the development of ore processing technology has made it possible to obtain high-grade fine ore.
Pelletizing methods have rapidly become popular. The mainstream of making fine ore pellets was to use a drum-type or pan-type granulator with an appropriate moisture content, and then granulate and then fire the pellets. However, from the viewpoint of energy saving and environmental protection, the firing process Instead, a cold pellet method using ordinary Portland cement as a binder is used. [Problems to be solved by the invention] Normally, the minimum strength when carrying pellets horizontally (primary handling strength) is approximately 5 to 20 kgf/cm 2 , and the minimum strength when charging pellets to the blast furnace (secondary handling strength) is approximately 30 to 20 kgf/cm 2
100Kgf/cm 2 is required. However, when Portland cement is used as a binder, a curing period of 7 to 14 days is required until a predetermined strength is obtained, and the pellets are often pulverized while being held horizontally. [Means for Solving the Problems] The present inventors have conducted various studies in order to develop pellet strength in a short time and solve the above problems, and have finally completed the present invention. That is, the present invention is a quick setting agent for cold pellets comprising calcium aluminate, divalent metal hydroxide, and monovalent metal carbonate. The present invention will be explained in detail below. Calcium aluminates (hereinafter referred to as CA) used in the present invention include 3CaO・Al 2 O 3 , 12CaO・
7Al 2 O 3 , CaO・Al 2 O 3 , CaO・2Al 2 O 3 and CaO・
Examples include crystalline and amorphous materials such as 6Al 2 O 3 . When the CaO/Al 2 O 3 molar ratio in CA is high, rapid setting is strong;
When the CaO/Al 2 O 3 molar ratio is low, the rapid setting becomes weak.
Therefore, the CaO/Al 2 O 3 molar ratio is preferably 0.5 to 4.0, more preferably 1.0 to 2.5. Divalent metal hydroxide (hereinafter referred to as M(OH) 2 )
Examples include calcium hydroxide, magnesium hydroxide, iron hydroxide, zinc hydroxide, manganese hydroxide, etc. Calcium hydroxide is economically preferred. The amount of M(OH) 2 added is 10 parts by weight of CA100.
-200 parts by weight is preferred, and 50-150 parts by weight is more preferred. Monovalent metal carbonates (hereinafter referred to as M 2 CO 3 ) include sodium carbonate, potassium carbonate, etc., but sodium carbonate is preferred from the economic standpoint. The amount of M 2 CO 3 added is 10 to 100 parts by weight of CA.
100 parts by weight is preferred, and 20 to 50 parts by weight is more preferred. The reason why we decided to use CA, M(OH) 2 and M 2 CO 3 together in the present invention is because the properties of pellets at high temperatures (hereinafter referred to as high temperature properties) are important when actually used in blast furnaces. ) becomes defective. That is, fine ore pellets need to have good pellet properties at room temperature and high temperature properties, and damage to the blast furnace becomes a serious problem especially when the alkali content in the ingredients is high. The alkaline content in cold pellets is approximately 0.1
It is preferable that the amount is less than % by weight. Furthermore, sulfur content such as SO 3 and chlorine content both have a negative effect on the blast furnace. The present invention suppresses these harmful components as much as possible. A quick setting agent consisting of CA, M(OH) 2 and M 2 CO 3 is used together with a hydraulic substance such as cement to granulate ore powder into cold pellets. Examples of the hydraulic substance include ordinary Portland cement, blast furnace cement, fly ash cement, silica cement, granulated blast furnace slag, and converter slag. From a physical standpoint, ordinary cement is preferable, but from an economic standpoint, it is preferable to use industrial by-products, and granulated blast furnace slag is even more preferable. The mixing ratio of the quick setting agent and the hydraulic substance of the present invention is preferably 1 to 20 parts by weight, more preferably 3 to 10 parts by weight, based on 100 parts by weight of the hydraulic substance. The amount of the hydraulic substance added is preferably 3 to 15 parts by weight, more preferably 5 to 12 parts by weight, per 100 parts by weight of fine ore. If the amount of the hydraulic substance added is less than this, the strength development will be poor, and if it is more than this, the content of the active ingredient will decrease and the benefits will decrease. The method of adding each component of the quick-setting agent and the hydraulic substance is not particularly limited, and the order of addition is not particularly limited. In order to improve the workability and strength properties of the kneaded product, commonly used cement water reducers, retarders and
Cement admixtures such as AE agents can be used together. In addition, monovalent sulfates, aluminates, hydrogen carbonates, phosphates, etc. can also be used in part. [Example] The present invention will be further explained in the following example. Example 1 The compositions were blended as shown in Experiment Nos. 6 to 15 in Table 1 and kneaded for 3 minutes using a mortar mixer (JISR-5201).
After that, it was poured into a 2 x 2 x 8 cm formwork and air-dried at 20°C. Handling time and compressive strength were measured. The results are shown in Table-2.

【表】【table】

【表】 註 配合量は重量部
<使用材料> 粉鉱石:ヘマタイト鉱 石灰石:市販品 水硬性物質A:普通ポルトランドセメント、電気
化学工業(株)製 〃 B:高炉水砕スラグ
ブレーン5020cm2/g CA:電気炉で溶融後吹き飛ばして急冷したもの
の粉砕品 Ca(OH)2:水酸化カルシウム、秩父石灰(株)製、
消石灰 Na2CO3:炭酸ナトリウム、旭硝子(株)製、軽灰
[Table] Note: Amounts are in parts by weight <Materials used> Ore powder: Hematite ore limestone: Commercial product Hydraulic substance A: Ordinary Portland cement, manufactured by Denki Kagaku Kogyo Co., Ltd. B: Granulated blast furnace slag
Brain 5020cm 2 /g CA: Pulverized product Ca (OH) 2 melted in an electric furnace, blown away and rapidly cooled. Calcium hydroxide, manufactured by Chichibu Lime Co., Ltd.
Slaked lime Na 2 CO 3 : Sodium carbonate, manufactured by Asahi Glass Co., Ltd., light ash

【表】 次に、表−1実験No.7,10の配合の混合物をモ
ルタルミキサーで水を添加しながら約3分間混練
した後、パン型造粒機(内径60cm)を用い、水を
少量滴下しながら造粒を行い、外径10〜20cmのペ
レツトを得て、20℃の気乾養生を7日間行つた。
造粒したペレツトを図面の装置のるつぼに入れ、
各温度で還元性状及び収縮性状を測定した。結果
を表−3に示す。 測定方法は、底に0.8cmの穴を10個穿孔した内
径4.8cmのるつぼにペレツトを200g入れ、その上
部及び下部には寸法1.1cm程度のコークスを約3
cmの厚さに詰めた。窒素気流中で10℃/分の昇温
速度で炉を加熱し、800℃で10分間保持し、その
後、CO30%、N270%の還元ガスを6.14Nl/分流
し、5℃/分の昇温速度で1500℃まで加熱しそれ
以後は1500℃一定とした。 還元率は出口ガスのCOとCO2の分析値より求
めた。
[Table] Next, the mixtures of Table 1 Experiment Nos. 7 and 10 were kneaded for about 3 minutes while adding water using a mortar mixer, and then a small amount of water was added using a pan-shaped granulator (inner diameter 60 cm). Pellets were granulated while dropping to obtain pellets with an outer diameter of 10 to 20 cm, and air-dried at 20°C for 7 days.
Put the granulated pellets into the crucible of the device shown in the drawing,
Reduction properties and shrinkage properties were measured at each temperature. The results are shown in Table-3. The measurement method is to put 200g of pellets into a crucible with an inner diameter of 4.8cm with ten 0.8cm holes drilled in the bottom, and about 30g of coke about 1.1cm in size to the top and bottom of the crucible.
Packed to cm thickness. The furnace was heated at a heating rate of 10°C/min in a nitrogen stream, held at 800°C for 10 minutes, and then a reducing gas of 30% CO and 70% N 2 was flowed at 6.14 Nl/min at a rate of 5°C/min. The temperature was increased to 1500℃, and the temperature was kept constant at 1500℃ thereafter. The reduction rate was determined from the analysis values of CO and CO 2 in the outlet gas.

〔発明の効果〕〔Effect of the invention〕

以上のように本発明のコールドペレツト用急結
剤を使用すると、従来の普通ポルトランドセメン
トのみのコールドペレツトに比べ数時間で数日養
生に匹敵する強度が得られるため、プロセスが非
常に簡略化され、ストツクヤードもそれ程必要と
せず経済的である。 又、高温性状も普通ポルトランドセメント使用
のコールドペレツトと比べ同等もしくはそれ以上
の性能が期待できる。
As described above, when the cold pellet accelerating agent of the present invention is used, the process is extremely simple, as strength comparable to that of several days of curing can be obtained in a few hours compared to conventional cold pellets made only of ordinary Portland cement. It is economical and does not require much stockyard. In addition, it is expected that the high-temperature properties will be equivalent to or better than cold pellets made using ordinary Portland cement.

【図面の簡単な説明】[Brief explanation of the drawing]

図面はコールドペレツトの高温性状を測定する
装置の一例である。 符号、1……ガス流量計、2……サンプリング
箱、3……熱電対、4……反応管、5……黒鉛る
つぼ、6……コークス層、7……コールドペレツ
ト、8……収縮計、9……分銅、10……差圧
計、11……ガス分析計。
The drawing shows an example of an apparatus for measuring the high temperature properties of cold pellets. Code, 1...Gas flow meter, 2...Sampling box, 3...Thermocouple, 4...Reaction tube, 5...Graphite crucible, 6...Coke layer, 7...Cold pellet, 8...Contraction Meter, 9... Weight, 10... Differential pressure gauge, 11... Gas analyzer.

Claims (1)

【特許請求の範囲】[Claims] 1 カルシウムアルミネート、2価の金属水酸化
物及び1価の金属炭酸塩からなるコールドペレツ
ト用急結剤。
1. Rapid setting agent for cold pellets consisting of calcium aluminate, divalent metal hydroxide, and monovalent metal carbonate.
JP19871484A 1984-09-25 1984-09-25 Accelerator for cold pellet Granted JPS6177651A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19871484A JPS6177651A (en) 1984-09-25 1984-09-25 Accelerator for cold pellet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19871484A JPS6177651A (en) 1984-09-25 1984-09-25 Accelerator for cold pellet

Publications (2)

Publication Number Publication Date
JPS6177651A JPS6177651A (en) 1986-04-21
JPH0573707B2 true JPH0573707B2 (en) 1993-10-14

Family

ID=16395784

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19871484A Granted JPS6177651A (en) 1984-09-25 1984-09-25 Accelerator for cold pellet

Country Status (1)

Country Link
JP (1) JPS6177651A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006062888A (en) * 2004-08-24 2006-03-09 Taiheiyo Material Kk Quick-hardening admixture and quick-hardening cement composition
JP5466799B2 (en) * 2008-04-04 2014-04-09 株式会社 テツゲン Zn-containing dust agglomerate and method for producing the same
JP4878044B2 (en) * 2008-08-20 2012-02-15 電気化学工業株式会社 Solidified material for increasing hot strength of ore powder, ore powder pellets using the same, and method for producing the same

Also Published As

Publication number Publication date
JPS6177651A (en) 1986-04-21

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