JPH0598338A - Slag reforming agent and method for refoming refining slag - Google Patents
Slag reforming agent and method for refoming refining slagInfo
- Publication number
- JPH0598338A JPH0598338A JP3283883A JP28388391A JPH0598338A JP H0598338 A JPH0598338 A JP H0598338A JP 3283883 A JP3283883 A JP 3283883A JP 28388391 A JP28388391 A JP 28388391A JP H0598338 A JPH0598338 A JP H0598338A
- Authority
- JP
- Japan
- Prior art keywords
- slag
- refining
- powder
- modifier
- produced
- 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.)
- Pending
Links
- 239000002893 slag Substances 0.000 title claims abstract description 107
- 238000007670 refining Methods 0.000 title claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 8
- 238000000034 method Methods 0.000 title claims description 12
- 238000002407 reforming Methods 0.000 title abstract description 13
- 239000000843 powder Substances 0.000 claims abstract description 10
- 239000003607 modifier Substances 0.000 claims description 27
- 229910052751 metal Inorganic materials 0.000 claims description 21
- 239000002184 metal Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 238000003723 Smelting Methods 0.000 claims description 4
- 238000000151 deposition Methods 0.000 claims 1
- 239000000428 dust Substances 0.000 abstract description 7
- 238000001816 cooling Methods 0.000 abstract description 6
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 abstract description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 5
- 229910000831 Steel Inorganic materials 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000010959 steel Substances 0.000 abstract description 4
- 239000000463 material Substances 0.000 abstract description 3
- 238000000227 grinding Methods 0.000 abstract description 2
- 229910052742 iron Inorganic materials 0.000 abstract 2
- 230000000694 effects Effects 0.000 description 6
- 238000009628 steelmaking Methods 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- -1 boric acid compound Chemical class 0.000 description 2
- JHLNERQLKQQLRZ-UHFFFAOYSA-N calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 2
- 229910052918 calcium silicate Inorganic materials 0.000 description 2
- 235000012241 calcium silicate Nutrition 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910001678 gehlenite Inorganic materials 0.000 description 2
- 235000013980 iron oxide Nutrition 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052867 ilvaite Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000003832 thermite Substances 0.000 description 1
Classifications
-
- 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
- Furnace Details (AREA)
- Carbon Steel Or Casting Steel Manufacturing (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、電気炉、転炉において
発生するスラグの崩壊防止を目的としたスラグ改質剤及
び精錬スラグの改質方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a slag modifier for refining slag generated in electric furnaces and converters, and a method for modifying refining slag.
【0002】[0002]
【従来の技術】一般に製鋼過程で発生するスラグ、特に
電気炉の還元スラグは崩壊風化されるが、これは未反応
の遊離石灰に起因するとされ、水冷時の水と反応し、更
に空気中の炭酸ガスを吸収し、炭酸カルシウムに変化し
微粉末となって粉塵の原因になっている。そこで、この
問題点を解決するため、スラグの崩壊防止を図る方法と
して、特開昭55−138016号公報に示すようにス
ラグ温度より低温で溶融する粘板岩や頁岩を投入し、外
部より熱を供給してスラグ組成を変化させ、スラグの崩
壊防止を行う方法や、特開昭61−295263号公報
に示されるように熱源コストを削減する為に金属アルミ
ニウムを添加し、他の酸化鉄と反応させて発生する反応
熱を利用してコスト削減を行い、スラグの改質を行う方
法が提案されていた。また、特開昭62−162657
号公報に示すように、ダイカルシウムシリケートを主体
とする製鋼溶融スラグに、スラグ冷却時の粉化を防止す
る為に硼酸あるいは硼酸化合物を添加してその改質を図
る方法が提案されていた。2. Description of the Related Art Generally, the slag generated in the steelmaking process, especially the reducing slag of an electric furnace, is collapsed and weathered, which is attributed to unreacted free lime, which reacts with water during water cooling and further in the air. It absorbs carbon dioxide, changes to calcium carbonate and becomes fine powder, which causes dust. Therefore, in order to solve this problem, as a method for preventing collapse of slag, as shown in JP-A-55-138016, slate or shale that melts at a temperature lower than the slag temperature is charged and heat is supplied from the outside. Then, the slag composition is changed to prevent the slag from collapsing, and as shown in JP-A-61-295263, metallic aluminum is added to react with other iron oxides in order to reduce the heat source cost. There has been proposed a method of reforming the slag by reducing the cost by using the reaction heat generated as a result. In addition, JP-A-62-162657
As disclosed in the publication, there has been proposed a method of adding boric acid or a boric acid compound to a steelmaking molten slag mainly composed of dicalcium silicate in order to prevent pulverization at the time of cooling the slag, thereby improving the slag.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、前記特
開昭61−295263号公報記載のように、外部より
熱を供給するので割高になり、更には特開昭61−29
5263号公報に示されるように反応熱を利用する方法
は、テルミット反応を起こさせる為に、金属アルミニウ
ムや酸化鉄が必要であり、改質材の原料及び製造コスト
が割高になるという問題点があった。また、特開昭62
−162657号公報に示される方法においては、前記
製鋼スラグに硼酸あるいは硼酸化合物を添加しても発塵
が激しく、添加剤の損失が大きいという問題点と、精錬
スラグによっては確実な改質を行い得ないという問題点
があった。本発明はこのような事情に鑑みてなされたも
ので、比較的製造及び使用コストが安く添加効率の良い
スラグ改質剤及び精錬スラグの改質方法を提案すること
を目的とする。However, as described in JP-A-61-295263, the heat is supplied from the outside, so that the cost is high, and further, JP-A-61-29.
The method using reaction heat as disclosed in Japanese Patent No. 5263 requires metal aluminum or iron oxide in order to cause the thermite reaction, and thus has a problem that the raw material of the modifier and the manufacturing cost are relatively high. there were. In addition, JP-A-62
In the method disclosed in Japanese Patent Laid-Open No. 162657/1992, even if boric acid or a boric acid compound is added to the steelmaking slag, the dust is intense and the loss of the additive is large, and certain refining slag is used for reliable reforming. There was a problem that I could not get it. The present invention has been made in view of the above circumstances, and an object thereof is to propose a slag modifier and a method for modifying refining slag that are relatively inexpensive to manufacture and use and have good addition efficiency.
【0004】[0004]
【課題を解決するための手段】前記目的に沿う請求項第
1項記載のスラグ改質剤は、溶銑脱珪スラグを含水させ
て0.1〜1.0%の水分を有するようにし、そして、
該溶銑脱珪スラグに内分にて25〜30%のB2 O3 粉
を付着させている。The slag modifier according to claim 1, which is in accordance with the above object, contains a hot metal desiliconization slag to have a water content of 0.1 to 1.0%, and ,
25-30% of B 2 O 3 powder is adhered internally to the hot metal desiliconization slag.
【0005】また、前記目的に沿う請求項第2項記載の
精錬スラグの改質方法は、0.1〜1.0%の水分を含
有する溶銑脱硅スラグに、内分にて25〜30%のB2
O3 粉を付着させ、しかも改質されたスラグのB2 O3
濃度が0.6〜1.5%となるような量の改質剤を取鍋
底に床敷して精錬スラグを投入し、該スラグの改質を行
うようにしている。According to the second aspect of the present invention, there is provided a method for modifying a smelting slag according to the second aspect, in which 25-30, in internal content, of hot-melted hot metal deslagging slag containing 0.1 to 1.0% of water is contained. % B 2
B 2 O 3 of slag modified with O 3 powder attached
An amount of the modifying agent having a concentration of 0.6 to 1.5% is laid on the bottom of the ladle, and refining slag is added to modify the slag.
【0006】[0006]
【作用】本発明のスラグ改質剤及び精錬スラグの改質方
法において重要なことは、改質剤のスラグとの反応の迅
速化と精錬スラグに添加する際に発塵をすることにある
との知見を得た。また、本発明は改質剤の基材として溶
銑脱硅処理後の溶銑脱硅スラグを用いることにある。こ
れは、溶銑脱硅スラグが粒子状であっても、これ自体が
易溶融性の低融点化合物を形成しており、添加後速やか
に精錬スラグに混合するからである。なお、実験によれ
ばB2 O3 を30%含む脱硅スラグのその融点が970
℃程度であった。In the slag modifier and the method for modifying the smelting slag of the present invention, it is important to accelerate the reaction of the modifier with the slag and to generate dust when added to the slag. I got the knowledge of. Further, the present invention is to use the hot metal desiliconized slag after the hot metal desiliconization treatment as the base material of the modifier. This is because even if the hot metal demolition slag is in the form of particles, it itself forms a low-melting compound that is easily meltable, and is quickly mixed with the smelting slag after addition. According to the experiment, the melting point of the desiliconized slag containing 30% of B 2 O 3 is 970.
It was about ℃.
【0007】そして、この溶銑脱硅スラグに水分を0.
1〜1.0%含水あるいは付着せしめて、B2 O3 粉を
付着固化させる。この付着固化によって精錬スラグに添
加あるいは床敷時にB2 O3 を含めた粉物の発塵を防止
し、しかも表面に精錬スラグ改質特性の優れたB2 O3
粉を露出させた改質材である為、B2 O3 の改質効果が
大幅に向上する。しかも、このB2 O3 効果は先に述べ
た溶銑脱硅スラグの特性と相乗して精錬スラグの改質効
果が迅速かつ確実に発現される。また、改質剤中のB2
O3 濃度は、その改質能から25〜30%とすると共
に、該改質剤を用いて改質処理を行ったスラグのB2 O
3 濃度が0.6〜1.5%となるようにする。ここで、
溶銑脱硅スラグに含水または付着する水分が0.1%よ
り低いとB2 O3 を溶銑脱硅スラグ粒に充分に付着でき
ず、添加時に発塵とB2 O3 の損失を招く。一方、B2
O3 の量が1.0%より多いと添加時に急激な加熱によ
る水蒸気に起因した急激な発塵とB2 O3 の損失を招
く。Then, water is added to the hot metal de-slagging slag.
B 2 O 3 powder is adhered and solidified by containing 1 to 1.0% of water or adhering it. This attachment solidified prevent dust generation Konabutsu including B 2 O 3 in addition or during bedding in refining slag, yet excellent B 2 O 3 of refining slag reforming properties to the surface
Since it is a modifier in which powder is exposed, the effect of modifying B 2 O 3 is greatly improved. Moreover, this B 2 O 3 effect is synergistic with the above-mentioned characteristics of the hot metal de-slagging slag, and the reforming effect of the refining slag is rapidly and surely exhibited. In addition, B 2 in the modifier
The O 3 concentration is 25 to 30% due to its reforming ability, and B 2 O of slag subjected to the reforming treatment using the modifying agent.
3 Make the concentration 0.6-1.5%. here,
If the amount of water contained in or attached to the hot metal de-slagging slag is lower than 0.1%, B 2 O 3 cannot be sufficiently adhered to the hot metal de-slagging slag particles, leading to dust generation and loss of B 2 O 3 when added. On the other hand, B 2
If the amount of O 3 is more than 1.0%, rapid heating at the time of addition causes rapid dust generation due to water vapor and loss of B 2 O 3 .
【0008】また、改質剤中のB2 O3 濃度が25%よ
り少ないと、不安定なα´−2CaO・SiO2 が、γ
−2CaO・SiO2 となり易いという問題がある。一
方、改質剤中のB2 O3 濃度が30%より多いと必要以
上のB2 O3 添加となり、経済上の問題がある。次に、
改質後の精錬スラグ中のB2O3 の濃度が0.6%より
低いとスラグの改質効果が不安定となる点で問題があ
り、逆に1.5%より多いと必要以上のB 2 O3 添加と
なり、経済上の問題がある。In addition, B in the modifier2O3The concentration is 25%
If it is less, unstable α'-2CaO ・ SiO2But γ
-2CaO / SiO2There is a problem that it easily becomes. one
B in the modifier2O3If the concentration is higher than 30%, it is not necessary.
B above2O3It becomes an addition, and there is an economic problem. next,
B in refined slag after reforming2O3Concentration of 0.6%
If it is low, there is a problem that the slag reforming effect becomes unstable.
On the contrary, if it is more than 1.5%, B is more than necessary. 2O3With addition
There are financial problems.
【0009】そして、該スラグ改質剤には、25〜40
%のCaO、20〜30%のSiO2 及び2〜4%のA
l2 O3 を含んでいるので、スラグの成分を調質すると
共に、B2 O3 の溶融製鋼スラグの拡散混合を助長す
る。なお、この範囲を越えると塩基度が高くなったりし
てスラグの流動性が悪くなり、場合によっては前記した
安定した鉱物組成への改質が行われないことが生ずる。The slag modifier contains 25 to 40
% CaO, 20-30% SiO 2 and 2-4% A
because it contains l 2 O 3, as well as tempered components of the slag, to promote diffusive mixing of the molten steel slag B 2 O 3. If it exceeds this range, the basicity will become high and the fluidity of the slag will deteriorate, and in some cases the above-described stable mineral composition may not be modified.
【0010】[0010]
【実施例】まず、本発明の一実施例に係るスラグ改質剤
を製造するに当たっては溶銑脱珪スラグを用意する。こ
の溶銑脱珪スラグの粒度は表1の通りである。EXAMPLES First, in producing a slag modifier according to an example of the present invention, hot metal desiliconization slag is prepared. The particle size of this hot metal desiliconization slag is as shown in Table 1.
【0011】[0011]
【表1】 [Table 1]
【0012】次に、該溶銑脱珪スラグをミキサーに入れ
て0.1〜1.0%の水分を有するように加水し、次に
内分で25〜30%のB2 O3 を入れて攪拌し、破砕さ
れた溶銑脱珪スラグにB2 O3 を略均等に混入して製造
する。なお、この例においては、スラグ改質剤の原料と
して溶銑脱珪スラグを使用したが、全体的成分が上記範
囲に入るものであれば、他の原料あるいは不足分を混入
して調整した原料であっても使用可能である。Next, the hot metal desiliconization slag is put into a mixer and water is added so as to have a water content of 0.1 to 1.0%, and then 25 to 30% of B 2 O 3 is added as an internal content. It is manufactured by mixing B 2 O 3 into the crushed hot metal desiliconization slag that has been stirred and crushed substantially uniformly. In this example, hot metal desiliconization slag was used as the raw material for the slag modifier, but if the overall components fall within the above range, other raw materials or raw materials prepared by mixing in shortages may be used. It can be used even if there is.
【0013】このスラグ改質剤を使用する場合には、予
め該スラグ改質剤を受滓鍋に入れておくが、その投入量
は処理しようとするスラグの1〜7%(好ましくは3〜
5%)程度とする。次に、溶融製鋼スラグを該受滓鍋に
受滓するが、この場合、前記スラグ改質剤は、受滓時に
溶融製鋼スラグの落下エネルギーによって攪拌され、ス
ラグの溶融点を下げると同時に、スラグの改質を行う。When using this slag modifier, the slag modifier is put in a slag pan in advance, but the amount of the slag modifier is 1 to 7% (preferably 3 to 7) of the slag to be treated.
5%). Next, the molten steelmaking slag is received in the slag pan, in which case the slag modifier is agitated by the falling energy of the molten steelmaking slag at the time of slag to lower the melting point of the slag and at the same time. Is modified.
【0014】24時間徐冷を進めると、スラグ改質剤を
添加していないスラグは早いもので4〜5時間後には全
て粉化し、処理作業に困難をきたすが、該スラグ改質剤
を添加したスラグは粉化が充分防止され、その後、水に
浸漬しても崩壊を起こさない。ここで、本発明の作用効
果を確認する為に実験を行ったので、その結果について
説明すると、まず、処理対象のスラグの成分を表2に示
し、表3には実験したスラグ改質剤(A)、(B)、
(C)の成分とX線回析の結果を示す。When gradual cooling is continued for 24 hours, the slag without addition of the slag modifier is early and after 4 to 5 hours all are pulverized, which causes difficulty in treatment work, but the slag modifier is added. The slag thus produced is sufficiently prevented from being pulverized and does not disintegrate even if it is immersed in water thereafter. Here, an experiment was conducted in order to confirm the action and effect of the present invention. The results will be described. First, the components of the slag to be treated are shown in Table 2, and Table 3 shows the experimental slag modifier ( A), (B),
The component (C) and the result of X-ray diffraction are shown.
【0015】[0015]
【表2】 [Table 2]
【0016】[0016]
【表3】 [Table 3]
【0017】従って、X線回析結果により、電気炉還元
スラグで粉化崩壊の原因となるγ形ダイカルシウムシリ
ケート(γ−2CaO・SiO2 )はアルミン酸塩によ
って、ゲーレナイト(GEHLENITE、2CaO・
SiO2 ・Al2 O3 )となり、安定したものと考えら
れる。(B)、(C)については改質後のゲーレナイト
比が90%以上と高く、また(A)については、イルバ
イト(ILVAITE、CaO・Fe2 O3 (FeO
H)・SiO2 )と、ゲーレナイトが殆どで安定である
と推察される。また、溶銑脱珪スラグをベースとした改
質剤はスラグ処理後の粉化防止剤としては充分適用可能
であることが明らかとなった。なお、B2 O3 (無水硼
酸)は原料として比較的高価であるので、スラグ改質剤
の30%以下で充分であると考えられる。また、前記実
施例においてスラグ改質剤は受滓鍋の底に予め入れて置
く入れ置き型を採用したが、ガスによる吹き込み型、上
置き型であっても良い。Therefore, according to the result of X-ray diffraction, the γ-type dicalcium silicate (γ-2CaO.SiO 2 ) which causes the powdering and disintegration in the electric furnace reducing slag is converted to the glenite (GEHLENITE, 2CaO.
SiO 2 · Al 2 O 3 ) and is considered to be stable. For (B) and (C), the post-reforming Gerenite ratio is as high as 90% or more, and for (A), ilbitite (ILVAITE, CaO.Fe 2 O 3 (FeO
It is presumed that H) and SiO 2 ) and gehlenite are stable in most cases. Further, it has been clarified that the modifier based on hot metal desiliconization slag is sufficiently applicable as a dusting inhibitor after slag treatment. Since B 2 O 3 (boric anhydride) is relatively expensive as a raw material, it is considered that 30% or less of the slag modifier is sufficient. Further, in the above-mentioned embodiment, the slag modifier is of the put type which is put in the bottom of the slag pan in advance, but it may be blown by gas or put on top.
【0018】[0018]
【発明の効果】請求項第1項及び第2項に記載のスラグ
改質剤及び精錬スラグの改質方法は、そのまま放置する
と崩壊する製鋼過程で発生するスラグの崩壊を防止でき
るので、処理されたスラグを路盤材として使用でき、ス
ラグの利用範囲が拡大されることになった。そして、従
来品に比較して比較的製造及び使用コストが安く添加効
率の良いスラグ改質剤を提供できることになった。更に
は、従来有効な利用方法が無かった溶銑脱珪スラグを利
用できるので、更にスラグの利用方法が拡大された。EFFECTS OF THE INVENTION The slag modifier and refining slag reforming method according to claims 1 and 2 are treated because they can prevent the slag from collapsing in the steelmaking process, which is disintegrated if left as it is. The slag can be used as a roadbed material, and the application range of slag is expanded. And, it has become possible to provide a slag modifier which is relatively low in manufacturing and use costs as compared with conventional products and has good addition efficiency. Furthermore, since the hot metal desiliconization slag, which has not been effectively used in the past, can be used, the usage of slag is further expanded.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 斎藤 順一 福岡県北九州市八幡東区大谷1丁目3番1 号 入江興産株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Junichi Saito 1-3-1 Otani, Yawatahigashi-ku, Kitakyushu, Fukuoka Prefecture Irie Kosan Co., Ltd.
Claims (2)
1.0%の水分を有するようにし、そして、該溶銑脱珪
スラグに内分にて25〜30%のB2 O3 粉を付着させ
たことを特徴とするスラグ改質剤。1. Hot metal desiliconization slag is impregnated with water for 0.1 to 10.
A slag modifier characterized by having a water content of 1.0% and adhering 25 to 30% of B 2 O 3 powder in the internal content to the hot metal desiliconization slag.
脱硅スラグに、内分にて25〜30%のB2 O3 粉を付
着させ、しかも改質されたスラグのB2 O3 濃度が0.
6〜1.5%となるような量の改質剤を取鍋底に床敷し
て精錬スラグを投入し、該スラグの改質を行うことを特
徴とする精錬スラグの改質方法。2. A slag modified by depositing 25 to 30% of B 2 O 3 powder in the internal content on the hot metal desiliconized slag containing 0.1 to 1.0% of water. 2 O 3 concentration is 0.
A method for modifying a smelting slag, which comprises laying a modifying agent in an amount of 6 to 1.5% on the bottom of a ladle, adding refining slag, and modifying the slag.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3283883A JPH0598338A (en) | 1991-10-03 | 1991-10-03 | Slag reforming agent and method for refoming refining slag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3283883A JPH0598338A (en) | 1991-10-03 | 1991-10-03 | Slag reforming agent and method for refoming refining slag |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0598338A true JPH0598338A (en) | 1993-04-20 |
Family
ID=17671414
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3283883A Pending JPH0598338A (en) | 1991-10-03 | 1991-10-03 | Slag reforming agent and method for refoming refining slag |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0598338A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2022036364A (en) * | 2020-08-18 | 2022-03-08 | デンカ株式会社 | Cement admixture, and cement composition |
-
1991
- 1991-10-03 JP JP3283883A patent/JPH0598338A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2022036364A (en) * | 2020-08-18 | 2022-03-08 | デンカ株式会社 | Cement admixture, and cement composition |
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