JPS5850302B2 - How to generate slag that does not disintegrate - Google Patents
How to generate slag that does not disintegrateInfo
- Publication number
- JPS5850302B2 JPS5850302B2 JP50122136A JP12213675A JPS5850302B2 JP S5850302 B2 JPS5850302 B2 JP S5850302B2 JP 50122136 A JP50122136 A JP 50122136A JP 12213675 A JP12213675 A JP 12213675A JP S5850302 B2 JPS5850302 B2 JP S5850302B2
- Authority
- JP
- Japan
- Prior art keywords
- slag
- weight
- disintegrate
- 2cao
- heat
- 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
Links
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
- Processing Of Solid Wastes (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Furnace Details (AREA)
Description
【発明の詳細な説明】
本発明は崩壊しやすい転炉スラグをその鉱物組成を変化
させることにより、崩壊しないスラグを生成する方法に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing non-collapsing slag by changing the mineralogical composition of collapsible converter slag.
一般に転炉滓はγ及びβ−2CaO−8iO2主体でゲ
ーレナイト、アケルマナイト、フリーライム、マグネタ
イト、ウスタイト等を含有している。Generally, converter slag mainly contains gamma and beta-2CaO-8iO2 and contains gehlenite, akermanite, free lime, magnetite, wustite, and the like.
スラグが崩壊したり、膨張したりするため利用方法も少
く、現状では埋立等に利用されているが、公害防止上、
埋立地の確保等が難しくなり処分に困っている。Because slag disintegrates and expands, there are few ways to use it, and currently it is used for landfilling, etc., but for pollution prevention purposes,
It is becoming difficult to secure a landfill site, and disposal is becoming a problem.
これらスラグの崩壊原因を調べると、Ca (0H)2
、フリーライム(以下F−CaOとする)、CaO3及
びγ−2CaO−8iO□から構成しているのでCa
(OH) 2 、 Ca CO3の原因はF−CaOで
空気中及びスラグの冷却時に散水する水分を吸収し、C
a(OH)2更に、空気中からCO2を吸収し、CaC
O5に変っていることがわかる。When we investigate the cause of the collapse of these slags, we find that Ca(0H)2
, free lime (hereinafter referred to as F-CaO), CaO3 and γ-2CaO-8iO□, so Ca
(OH) 2, CaCO3 is caused by F-CaO, which absorbs moisture in the air and sprinkled during cooling of the slag, and
a(OH)2 further absorbs CO2 from the air and produces CaC
You can see that it has changed to O5.
そこで本願ではこれらの崩壊の原因たるF−CaO1及
びγ−2CaO−8iO2を安定な鉱物組成、すなわち
3CaO−Ag2O3,2CaO−Ag2O3・5iO
(ゲーレナイト)、2CaO−Mg0・2SiO2(ア
ケルマナイト)等に変化させることにより、急冷せずと
も崩壊しないスラグを生成する方法を提供するものであ
る。Therefore, in this application, F-CaO1 and γ-2CaO-8iO2, which are the causes of these collapses, are replaced by stable mineral compositions, namely 3CaO-Ag2O3, 2CaO-Ag2O3・5iO
(Gehlenite), 2CaO-Mg0.2SiO2 (Akermanite), etc., thereby providing a method for producing slag that does not disintegrate even without rapid cooling.
本願は、溶融状態にある転炉スラグに赤泥、粘板岩、頁
岩、真砂及び各種カラミの一種以上を添加しその最終組
成がAg2O34,1〜11,9重量%、S t021
1〜34.8重量%、CaO21,4〜38.4重量%
とする事で崩壊しないスラグを生成する方法に係るもの
である。In this application, one or more of red mud, slate, shale, sand, and various types of calamari are added to converter slag in a molten state, and the final composition is Ag2O34.1 to 11.9% by weight, St021.
1-34.8% by weight, CaO21.4-38.4% by weight
This relates to a method of producing slag that does not disintegrate by doing so.
ここでスラグが溶融状態にある間に上記の如く各種添加
物を添加するのは、溶融スラグの有する顕熱を有効に利
用する為であり、スラグが有する顕熱のみでは熱量が不
足する場合には、外部より所要手段にて上記混合物が溶
融反応を生起するに十分な量の外部熱の供給をするもの
である。The reason for adding various additives as mentioned above while the slag is in a molten state is to effectively utilize the sensible heat of the molten slag. The method is such that an amount of external heat sufficient to cause the above mixture to undergo a melting reaction is supplied from the outside by the necessary means.
また転炉スラグに上記添加物を加えるのは前述した如く
鉱物組成を3CaO・Ag2O3,2CaO−Ag2O
3゜2CaO−Mg0・2SiO2に変化させる為であ
り、この為にはその鉱物組成から判明する如く添加物と
してはAg2O3のみでも十分であるが、Ag2O3の
みでは溶融温度が高く反応が生起し難いという欠点があ
るためにS s 02 t A l 203を適量同時
添加する事により溶融温度の低下を促し、反応が十分に
起こる様にしたのである。Also, adding the above additives to converter slag changes the mineral composition to 3CaO・Ag2O3, 2CaO-Ag2O.
The purpose is to change it to 3゜2CaO-Mg0.2SiO2, and for this purpose, as revealed by its mineral composition, Ag2O3 alone is sufficient as an additive, but it is said that Ag2O3 alone has a high melting temperature and is difficult to cause a reaction. Because of this drawback, an appropriate amount of S s 02 t A 1 203 was added at the same time to reduce the melting temperature and ensure that the reaction occurred sufficiently.
上記添加物たる赤泥はFe2O3,Ag2O3,Na2
Oに富んでいるので低溶融物(約1220℃)である。The above additives, red mud, are Fe2O3, Ag2O3, Na2
Since it is rich in O, it has a low melting temperature (approximately 1220°C).
粘板岩及び頁岩は日本全土に比較的多く賦存し、比較的
に安価で入手可能でS 102 、Ae 203 。Slate and shale are found in relatively large quantities throughout Japan and can be obtained at relatively low prices.
F e 203等に富んでいるのでこれもまた低溶融物
(約1250℃)である。Since it is rich in F e 203 etc., it is also a low melting material (approximately 1250° C.).
下記第1表に赤泥、及び粘板岩の代表的組成を示す。Table 1 below shows typical compositions of red mud and slate.
なお、本発明方法では原則として、外部熱を供給するこ
となく溶融スラグの有する顕熱のみにより、溶融反応を
進行せしめるために、溶解反応物の融点は比較的低温度
に保たれることが必要であり、溶融スラグの有する顕熱
に加え、外部より所要熱源を供給する方法を採れば赤泥
、粘板岩等を比較的多量配合できるし、またこの様に外
部熱を加えると冷却を完了したスラグについても同様に
本発明方法が可能である。In addition, in the method of the present invention, in principle, the melting point of the molten reactant must be kept at a relatively low temperature in order to allow the melting reaction to proceed only by the sensible heat of the molten slag without supplying external heat. In addition to the sensible heat possessed by molten slag, if a method is adopted to supply the required heat source from the outside, a relatively large amount of red mud, slate, etc. can be added, and by adding external heat in this way, the slag that has been completely cooled can be The method of the present invention is also applicable to the following.
次に本願各混合物の組成を決定する為の試験及びその結
果を示す。Next, tests for determining the composition of each mixture of the present application and their results will be shown.
まず第2表に各種組成配合の試料(重量%)を示す。First, Table 2 shows samples (% by weight) with various compositions.
次に第3表に各種組成試料の配合割合(重量%)を示す
。Next, Table 3 shows the blending ratios (% by weight) of various composition samples.
次に第4表に各種組成試料配合物の溶倒温度■を示す。Next, Table 4 shows melting temperatures (■) of various composition sample formulations.
次に第5表に各種組成試料配合物からのスラグの生成鉱
物を示す。Next, Table 5 shows the minerals produced in slag from various composition sample formulations.
次に第7表に各種組成試料配合物からのスラグのオート
クレーブ試験結果を示す。Next, Table 7 shows the autoclave test results of slags from various composition sample formulations.
なおオートクレーブ試験とは、コンクリート及び骨材の
JIS試験法(200℃、20kg/i、3時間加熱)
でスラグ粒度10〜15關につき行い、10mrn以下
を粉化物とみなし粉化率を算出したものである。Note that the autoclave test refers to the JIS test method for concrete and aggregate (200℃, 20kg/i, heating for 3 hours)
This was carried out for slag particle sizes of 10 to 15 mrn, and the pulverization rate was calculated by considering slag particles of 10 mrn or less as pulverized products.
以上の結果、転炉スラグに赤泥や粘板岩等のように適当
量のAg2O,や5102等を含有する低溶融物を添加
すると、配合量によって3CaO・Aeρ3゜2CaO
−Mg0・2SiO2,2CaO−Ag2O3・SiO
2等が主に生成し、2CaO−8iO2やF−CaOが
なくなる。As a result of the above, when a low melting material containing an appropriate amount of Ag2O, 5102, etc., such as red mud or slate, is added to converter slag, 3CaO・Aeρ3゜2CaO
-Mg0.2SiO2,2CaO-Ag2O3.SiO
2 etc. are mainly produced, and 2CaO-8iO2 and F-CaO are eliminated.
更に多量配合するとガラスとなり、2Ca0・8102
やF−CaOは完全になくなり、殆んど崩壊しないスラ
グに変わる。If a larger amount is added, it becomes glass, and 2Ca0.8102
and F-CaO completely disappear and turn into slag that hardly disintegrates.
その化学成分は、転炉滓でSiO□11〜34.8゜A
g20s 4.1〜11.9 、 CaO21,4〜3
8.4重量%となるように配合すれば崩壊を防止できる
。Its chemical composition is SiO□11~34.8°A in the converter slag.
g20s 4.1~11.9, CaO21,4~3
If the content is 8.4% by weight, disintegration can be prevented.
転炉から出滓したスラグの温度はノロ鍋中のスラグで約
1500〜1550℃あり、1500℃と仮定すると顕
熱は45万Km/1(1500X0.3=450cat
/fj )となる。The temperature of the slag discharged from the converter is approximately 1500 to 1550℃ in the slag pot.Assuming that the temperature is 1500℃, the sensible heat is 450,000 Km/1 (1500X0.3=450cat).
/fj).
粘土類の溶解熱(付着水5%、結晶水10%と仮定する
と)は次のようになる。The heat of dissolution of clay (assuming 5% adhered water and 10% crystallized water) is as follows.
水の蒸発熱 8.8万Kcat/l (0,15xss
s−87,・m/、!iJ)粘度類の溶融に要する熱量
31.9月0Vt ((1−0,5) (1250X0
.3 )−318,細Vg〕1500−12so=25
o25oXo、3=75a1!7′、p 7s75K
mVt以上の結果、約18.4重量%溶解可能である(
実際にはノロ鍋の容量の犬、小、放熱の差異等もあるが
、20〜251のノロ鍋ならば20重量%までは溶解可
能である)。Heat of vaporization of water 88,000 Kcat/l (0.15xss
s-87,・m/,! iJ) Heat required for melting viscosity 31.9 months 0Vt ((1-0,5) (1250X0
.. 3)-318, fine Vg]1500-12so=25
o25oXo, 3=75a1!7', p 7s75K
As a result of mVt or higher, approximately 18.4% by weight can be dissolved (
In reality, there are differences in the capacity of the pot, such as the size of the pot, the size of the pot, and the heat dissipation, but if you use a pot with a size of 20 to 251, it is possible to melt up to 20% by weight.)
以上述べてきたように、本願方法によれば、現在崩壊、
膨張する為に未使用かつ処理にされ困っている転炉スラ
グを急冷する必要もなく、簡単にしかも迅速に崩壊、膨
張しないスラグとする事が出来ると共に、溶融スラグの
有する多大な顕熱を有効利用することが可能である。As mentioned above, according to the method of the present application, current collapse,
There is no need to rapidly cool converter slag, which is unused and difficult to dispose of due to expansion, and it can be easily and quickly turned into slag that does not collapse and expand, and the large sensible heat of molten slag can be effectively utilized. It is possible to use it.
又本願方法により製造されたスラグは崩壊、膨張が起ら
ない為にバラス、砂等に有効利用が可能で運搬等の取扱
いも容易である。Furthermore, since the slag produced by the method of the present invention does not disintegrate or expand, it can be effectively used as ballast, sand, etc., and is easy to transport and handle.
Claims (1)
A/20341〜11.9重量%、S 10211〜3
4.8重量%、CaO21,4〜38.4重量%となる
べき量の赤泥、粘板岩、頁岩、真砂及び各種カラミの一
種以上を添加し、崩壊しないスラグを生成する方法。1 The final composition of the converter slag in a molten state is A/20341-11.9% by weight, S 10211-3.
A method of producing slag that does not disintegrate by adding one or more of red mud, slate, shale, sand, and various types of karami in an amount to be 4.8% by weight and 1.4 to 38.4% by weight of CaO2.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50122136A JPS5850302B2 (en) | 1975-10-09 | 1975-10-09 | How to generate slag that does not disintegrate |
| US05/873,329 US4179279A (en) | 1975-10-09 | 1978-01-30 | Process for treating molten steel slag with red mud from aluminum industry |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50122136A JPS5850302B2 (en) | 1975-10-09 | 1975-10-09 | How to generate slag that does not disintegrate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5263166A JPS5263166A (en) | 1977-05-25 |
| JPS5850302B2 true JPS5850302B2 (en) | 1983-11-09 |
Family
ID=14828495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50122136A Expired JPS5850302B2 (en) | 1975-10-09 | 1975-10-09 | How to generate slag that does not disintegrate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5850302B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6032123U (en) * | 1983-08-11 | 1985-03-05 | 河西工業株式会社 | Bracket for mounting automotive interior parts |
| JPS6327708U (en) * | 1986-08-06 | 1988-02-23 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5591915A (en) * | 1978-12-30 | 1980-07-11 | Nippon Steel Corp | Modifying method for steel-making slag |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4859079A (en) * | 1971-11-27 | 1973-08-18 | ||
| US3822799A (en) * | 1972-01-07 | 1974-07-09 | Calumite Co | Method of producing blast furnace slag products |
-
1975
- 1975-10-09 JP JP50122136A patent/JPS5850302B2/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6032123U (en) * | 1983-08-11 | 1985-03-05 | 河西工業株式会社 | Bracket for mounting automotive interior parts |
| JPS6327708U (en) * | 1986-08-06 | 1988-02-23 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5263166A (en) | 1977-05-25 |
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