JPS62288155A - Limy refractory composition - Google Patents
Limy refractory compositionInfo
- Publication number
- JPS62288155A JPS62288155A JP61130484A JP13048486A JPS62288155A JP S62288155 A JPS62288155 A JP S62288155A JP 61130484 A JP61130484 A JP 61130484A JP 13048486 A JP13048486 A JP 13048486A JP S62288155 A JPS62288155 A JP S62288155A
- Authority
- JP
- Japan
- Prior art keywords
- limestone
- weight
- parts
- composition
- steel
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims description 21
- 235000019738 Limestone Nutrition 0.000 claims description 25
- 239000006028 limestone Substances 0.000 claims description 25
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 20
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims description 20
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 18
- 239000000395 magnesium oxide Substances 0.000 claims description 10
- 239000011775 sodium fluoride Substances 0.000 claims description 10
- 235000013024 sodium fluoride Nutrition 0.000 claims description 10
- 229910021538 borax Inorganic materials 0.000 claims description 9
- 239000004328 sodium tetraborate Substances 0.000 claims description 9
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 9
- 235000006408 oxalic acid Nutrition 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 description 18
- 239000010959 steel Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 9
- 238000010276 construction Methods 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 229910052749 magnesium Inorganic materials 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 150000004760 silicates Chemical class 0.000 description 3
- 239000002893 slag Substances 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229910000805 Pig iron Inorganic materials 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000011822 basic refractory Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 229910052839 forsterite Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000001055 magnesium Nutrition 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
発明の詳細な説明
本発明は、タンディツシュ等の溶鋼用容器内面の内張シ
材として使用される石灰質耐火組成物に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a calcareous refractory composition used as a lining material for the inner surface of a container for molten steel such as a tundish.
従来タンディツシュ等の溶鋼用容器の内張り材として、
マクネシア質を主成分とし、付着性の付与及びスラグの
浸透防止のために、シリカ微粉、粘土類等を添加した耐
火組成物が使用されている。Conventionally used as a lining material for molten steel containers such as tanditshu.
Fire-resistant compositions are used that contain maknesia as a main component and add fine silica powder, clay, etc. to provide adhesion and prevent slag penetration.
しかしながら、シリカ微粉、粘土類は高温域で不安定で
あ’j)、Si、0等のピックアップ源となり易く、鋼
の清浄化5il1品質の向上等の冶金効果を低下させて
しまい好ましくない。However, fine silica powder and clays are unstable in high temperature ranges, tend to become a pick-up source of Si, O, etc., and are undesirable because they reduce metallurgical effects such as improving the quality of steel cleaning.
また、鋼の不純物と反応し易いことによって鋼の清浄化
に有効な石灰(Cab) を主成分とする耐火組成物
も使用されている。ところが、石灰は、耐火組成物を容
器内面に内張シ施工するに際して、水で混練すると乾燥
中に消化し、内張シ施工した耐火組成物(以下施工体と
いう)の強度を著しく低下させる。そのため、石灰を含
有する耐火組成物を内張シ施工する場合、水を使用する
ことができず、作業は極めて困難である。Refractory compositions based on lime (Cab), which is effective in cleaning steel because it easily reacts with impurities in steel, are also used. However, when lime is mixed with water when lining the inner surface of a container with a refractory composition, it is digested during drying, significantly reducing the strength of the refractory composition applied as a lining (hereinafter referred to as a construction body). Therefore, when lining with a fireproof composition containing lime, water cannot be used and the work is extremely difficult.
そこで、熱分解によってCaOを生成する戻酸カルシウ
ム(CaCO3)を多量に含有し、水によって消化しな
い石灰石及び苦土石灰石を使用する試みがなされてきた
。ところが、石灰石及び苦土石灰石は、加熱時CaOを
生成するとともに炭酸ガス欠点を有している。従って、
これらを多量に使用すると、耐火組成物の強度が低下し
てしまう。しかも、容器内面への付着性も充分ではない
。Therefore, attempts have been made to use limestone and magnesia limestone, which contain a large amount of calcium rehydrate (CaCO3) that generates CaO through thermal decomposition and are not digested by water. However, limestone and magnesium limestone generate CaO when heated and also have the drawback of carbon dioxide gas. Therefore,
If these are used in large amounts, the strength of the refractory composition will decrease. Furthermore, the adhesion to the inner surface of the container is not sufficient.
上記問題点を解消するため、石灰石及び苦土石灰石に、
ケイ酸塩及び/又はリン酸塩並びに粘土類等の増粘筒だ
剤を添加した塩基性耐火物が提案されている(特公昭5
8−34423号、特公昭59−34674号)。ケイ
酸塩及びリン酸塩は、石灰石及び苦土石灰石を加熱する
ことによって生ずるCaOと高融点結合を形成し、加熱
時の耐火組成物の収縮を抑制する。また、粘土類の添加
によって、付着性が向上する。しかしながら、ケイ酸塩
及びリン酸塩は、Si 及びPのピックアップ源となり
、また粘土類等は上述の如く、Si及びOのピックアッ
プ源となるため、鋼の清浄化、鋼品質の向上環が充分に
なされず好ましくない。In order to solve the above problems, limestone and magnesia limestone,
Basic refractories to which thickening agents such as silicates and/or phosphates and clays have been added have been proposed (Japanese Patent Publication No. 5
No. 8-34423, Special Publication No. 59-34674). Silicates and phosphates form high melting point bonds with CaO produced by heating limestone and magnesia, and suppress shrinkage of the refractory composition during heating. Furthermore, adhesion is improved by adding clays. However, silicates and phosphates act as pick-up sources for Si and P, and as mentioned above, clays act as pick-up sources for Si and O, so it is not enough to purify steel and improve steel quality. Undesirable and undesirable.
本発明者は上記問題点に鑑み、鋭意研究を重ねた結果、
石灰石及び苦土石灰石に、シュウぼ、ホウ砂及びフッ化
ナトリウムを添加することによって、加熱時に高強度を
示し、鋼に悪影響を及ばさない内張り用耐火物が得られ
ることを見出し、本発明を完成した。In view of the above problems, the inventor has conducted extensive research and found that
It was discovered that by adding oxalium, borax and sodium fluoride to limestone and magnesium, a refractory for lining that exhibits high strength when heated and does not have a negative effect on steel can be obtained, and the present invention was developed. completed.
即ち本発明は、石灰石及び/又は苦土石灰石50〜10
0重鼠%と残部がマクネジアクリンカ−からなる耐火骨
材100重量部、シュウ酸0.5〜3宜量部、ホウ砂0
.5〜5重量部及びフッ化ナトリウム0.5〜5重世部
を含有する石灰質耐火組成物に係る。That is, the present invention uses limestone and/or magnesium limestone 50 to 10
100 parts by weight of refractory aggregate consisting of 0 weight percent and the balance being Macnezia linker, 0.5 to 3 parts of oxalic acid, 0 borax.
.. The present invention relates to a calcareous refractory composition containing 5 to 5 parts by weight and 0.5 to 5 parts by weight of sodium fluoride.
本発明においては、耐火骨材として、石灰石及び/又は
苦土石灰石を使用する。また、必要に応じて、耐溶損性
を向上させる丸めに、マクネジアクリンカーを、石灰石
及び/又は苦土石灰石の含有量と等量となる址を上限と
して併用してもよい。In the present invention, limestone and/or magnesia limestone is used as the refractory aggregate. Further, if necessary, MacNesia linker may be used in combination with the rounding to improve the erosion resistance, with the upper limit being equal to the content of limestone and/or magnesia limestone.
石灰石及び/又は苦土石灰石の含有量が50重量≦未溝
になると、加熱時に生成するC40′kkが少なくなシ
、溶鋼に接する面に生じるフォルステライト(425*
Oa )、スピネル(MfA1204)等の高融点化
合物によってCaOと溶鋼との接触をさまたげるため、
溶鋼の清浄化等の冶金効果が低下し好ましくない。石灰
石、苦土石灰石及びマクネジアクリンカ−0粒径は特に
制限されず、適宜選択すればよい。例えば、石灰石、苦
土石灰石及びマクネジアクリンカ−のいずれKついても
、3〜IM程度のもの、1〜0.151m程度のもめ及
び0.15鱈未満9ものを適宜混合して使用すればよい
。When the content of limestone and/or magnesia limestone is 50 weight ≦ ungrooved, less C40'kk is generated during heating, and forsterite (425*
Oa ), spinel (MfA1204) and other high melting point compounds prevent contact between CaO and molten steel.
This is undesirable because metallurgical effects such as cleaning of molten steel deteriorate. The particle size of limestone, magnesium limestone, and Macnesia linker 0 is not particularly limited, and may be selected as appropriate. For example, regardless of the K of limestone, magnesia limestone, and Macnesia linker, if the K is about 3 to IM, the one about 1 to 0.151 m, and the one less than 0.15 cod 9 can be appropriately mixed and used. good.
本発明では、シlつ酸、フッ化ナトリウム及びホウ砂を
併用することによって、鋼に悪影響を与えることなく、
主に室温から1200℃程度の広範な温度域において、
施工体の強度を高めることができる。In the present invention, by using silicic acid, sodium fluoride, and borax in combination, the steel can be treated without adversely affecting the steel.
Mainly in a wide temperature range from room temperature to about 1200℃,
The strength of the construction body can be increased.
シlつ酸は、耐火組成物の各原料を水で混練する際に、
石灰石及びl又は苦土石灰石と反応し、シュウ酸カルシ
ウムの微細な結晶となり、低温域におけるマトリックス
の充填材として施工体の強度付与に有効である。またシ
ュウ酸カルシウムは、赤熱するとフッ化ナトリウムの融
化助剤として働き、次いで炭酸カルシウムと一酸化炭素
とに分解するので施工体中には残留せず、鋼に悪影響を
及ぼさない。シュウ酸の配合量は、耐火骨材100重社
部に対し、0.5〜3重斌部程度とするのがよい。0.
5重量部未満では、上記の如き効果を充分に発現するこ
とができず、一方3重量部を越えると、原料を水で混練
する場合に、骨材との反応による炭酸ガスの発生址が多
くなシ、施工体の強度が低下する。Silicic acid is used when kneading each raw material of the fireproof composition with water.
It reacts with limestone and limestone or magnesium to form fine crystals of calcium oxalate, which is effective in imparting strength to construction bodies as a matrix filler in low temperature ranges. Furthermore, when calcium oxalate becomes red hot, it acts as a melting aid for sodium fluoride, and then decomposes into calcium carbonate and carbon monoxide, so it does not remain in the construction body and does not have any adverse effect on the steel. The blending amount of oxalic acid is preferably about 0.5 to 3 parts per 100 parts of the refractory aggregate. 0.
If the amount is less than 5 parts by weight, the above effects cannot be sufficiently exhibited, while if it exceeds 3 parts by weight, carbon dioxide gas is often generated due to reaction with aggregate when the raw materials are kneaded with water. Otherwise, the strength of the construction structure will decrease.
* ’+8 (”2B4’7 ・10 H2’ )は7
5°Cで溶融して結合剤として働き、次いで350〜4
00℃程度で脱水し白色の無水物となって固化する。こ
の固化物は、878°Cで溶融しカラス状透明体となシ
、再び結合剤として働く。更に、このガラス状透明体は
、金属酸化物を融解させるため、マトリックスの焼結を
促進する。また受鋼時には、造滓剤として働き、漠に悪
影響を及ぼさない。ホウ砂の配合量は、耐火骨材100
重量部に対し、0.5〜5重世部程度とするのがよい。*'+8 ("2B4'7 ・10 H2') is 7
Melt at 5 °C to act as a binder, then 350-4
It dehydrates at about 00°C and solidifies as a white anhydride. This solidified material melts at 878° C. and becomes a glass-like transparent body, again acting as a binder. Additionally, the glassy transparency melts the metal oxide and thus promotes sintering of the matrix. Also, during steel receiving, it acts as a slag-forming agent and does not have any negative effects. The blending amount of borax is 100% of fireproof aggregate.
The amount is preferably about 0.5 to 5 parts by weight.
0.5mM部未満では、結合剤としての効果が少なく、
一方5重量部を越えると、造滓剤としての働きが強くな
り、施工体の耐食性が低下する。If it is less than 0.5mM, it has little effect as a binder;
On the other hand, if the amount exceeds 5 parts by weight, the action as a slag forming agent becomes stronger and the corrosion resistance of the construction object decreases.
フッ化ナトリウムは融点が992°Cであり、融点より
低い温度域では、焼結剤としてmき、融解した後では結
合剤として作用する。また受銑時には、ホウ砂と同様に
m滓剤として働くため、鋼の清浄化に有効である。フッ
化ナトリウムの配合量は、耐火骨材100重量部に対し
、0.5〜5!ffi部程度とするのがよい。0.5重
量部未満では、結合剤として効果が現われず、一方5重
量部を越えると、ホウ砂と同様に造滓剤としての働きが
強くなり、施工体の耐食性が低下する。また、施工時の
作業性向上のため本発明組成物に、ポリビニルアルコー
ル、ポリエチレンオ十サイド等の水溶性高分子物質を添
加することもできる。Sodium fluoride has a melting point of 992°C, and at temperatures below the melting point, it acts as a sintering agent, and after melting, it acts as a binder. Also, during pig iron receiving, it acts as a slag agent like borax, so it is effective in cleaning steel. The blending amount of sodium fluoride is 0.5 to 5 parts by weight per 100 parts by weight of the refractory aggregate! It is preferable to set it to about the ffi section. If it is less than 0.5 parts by weight, it will not be effective as a binder, while if it exceeds 5 parts by weight, it will act strongly as a slag-forming agent, similar to borax, and the corrosion resistance of the construction object will decrease. Furthermore, water-soluble polymeric substances such as polyvinyl alcohol and polyethylene oxide may be added to the composition of the present invention to improve workability during construction.
本発明組成物は、上記各種原料を所定量混合して製造さ
れる。The composition of the present invention is produced by mixing predetermined amounts of the above-mentioned various raw materials.
本発明組成物を溶鋼用容器内面に内張り施工するに際し
ては、本発明組成物に、耐火骨材100重量部に対しl
O〜20重景部程重量水を添加し、更に必要に応じて上
記水溶性高分子物質を添加してよく混練し、この混練物
をコテ塗シ等の通常の方法によって容器内面に塗布すれ
ばよい。When lining the inner surface of a container for molten steel with the composition of the present invention, 1 liter of the composition of the present invention is added to 100 parts by weight of refractory aggregate.
Add 0 to 20 parts of water by weight, and if necessary, add the water-soluble polymeric substance mentioned above and knead well. Apply this kneaded material to the inner surface of the container by a normal method such as applying with a trowel. Bye.
発明の効果
本発明組成物は、室温から1200°C程度の広い範囲
の温度域で、高強度を有し、また鋼の清浄化、画品質の
向上等の冶金効果にも優れている。Effects of the Invention The composition of the present invention has high strength in a wide temperature range from room temperature to about 1200°C, and also has excellent metallurgical effects such as cleaning steel and improving image quality.
以下に実施例及び比較例を挙げ、本発明をより一層明瞭
なものとする。Examples and comparative examples are given below to further clarify the present invention.
51!施例1,2
第1表に示す配合割合(重量部)で、石灰石100重祉
部に、シュウ酸、フッ化ナトリウム及びホウ砂を添加し
て混合し、本発明組成物を製造した。51! Examples 1 and 2 Oxalic acid, sodium fluoride, and borax were added and mixed to 100 parts of limestone in the proportions (parts by weight) shown in Table 1 to produce a composition of the present invention.
得られた本発明組成物に、第1表に示す配合割合(重量
部)で水を添加して混練し、内張シ材を製造した。得ら
れた内張シ材を強度試験に供した。Water was added to the obtained composition of the present invention in the proportions (parts by weight) shown in Table 1 and kneaded to produce a lining material. The obtained lining material was subjected to a strength test.
結果を第1表に示す。The results are shown in Table 1.
比較例1〜3
本発明組成物の必須成分であるシュウ酸、フッ化ナトリ
ウム及びボウ砂のうち、1種又は2種のみを使用する以
外は、fil!m例1.2と同様にして、第1表に示す
配合割合(重量部)で内張シ材を製造した。得られた内
張シ材を実施例1.2と同様の強度試験に供した。結果
を第1表に示す。Comparative Examples 1 to 3 Except for using only one or two of the essential components of the composition of the present invention, oxalic acid, sodium fluoride, and sand, fil! In the same manner as in Example 1.2, lining materials were produced using the blending ratios (parts by weight) shown in Table 1. The obtained lining material was subjected to the same strength test as in Example 1.2. The results are shown in Table 1.
※ 30X30X150sa*のテストピースをガスバ
ーナーの炎で直接加熱した。*A 30X30X150sa* test piece was directly heated with the flame of a gas burner.
第1表より、シュウ酸、フッ化ナトリウム及びホウ砂の
うちいずれかが欠けても、施工体の強度が低下すること
が判る@
実施例3〜5
実施例1.2と同様にして、第2表に示す配合割合(重
置部)で、本発明組成物を製造し、次いでこれに水を添
加して内張り材を製造した。得られた内*b材を、タン
ディツシュ内面に厚さ201にコテ塗〕施工し、100
0°Cで2時間予熱乾燥を行った。亀裂、剥離等は認め
られなかった。From Table 1, it can be seen that even if any one of oxalic acid, sodium fluoride, and borax is missing, the strength of the constructed body decreases. A composition of the present invention was produced at the blending ratio (overlapping portion) shown in Table 2, and then water was added thereto to produce a lining material. The obtained inner *b material was applied to the inner surface of the tundish to a thickness of 201 mm with a trowel.
Preheated drying was performed at 0°C for 2 hours. No cracks, peeling, etc. were observed.
このタンディツシュにアルミ中ルド鋼を受鋼し、内張り
材の状態を調べた。結果を第2表に示す。This tanditshu was made of aluminum cored steel and the condition of the lining material was examined. The results are shown in Table 2.
第2表
第2表よシ明らかなように、酸化物(非金属介在物)の
堆積が、従来品(マグネシア質内張シ材)に比べて著し
く減少し、ml中の非金属介在物の除去に有効で6りた
。As is clear from Table 2, the accumulation of oxides (non-metallic inclusions) is significantly reduced compared to the conventional product (magnesia-based lining material), and the amount of non-metallic inclusions per ml is significantly reduced. It was effective for removal and got 6 points.
(以 上)(that's all)
Claims (1)
残部がマグネシアクリンカーからなる耐火骨材100重
量部、シュウ酸0、5〜3重量部、ホウ砂0.5〜5重
量部及びフッ化ナトリウム0.5〜5重量部を含有する
石灰質耐火組成物。1 100 parts by weight of fireproof aggregate consisting of 50-100% by weight of limestone and/or magnesia limestone and the balance being magnesia clinker, 0.5-3 parts by weight of oxalic acid, 0.5-5 parts by weight of borax, and sodium fluoride. A calcareous refractory composition containing 0.5 to 5 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61130484A JPH0742163B2 (en) | 1986-06-04 | 1986-06-04 | Calcareous refractory composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61130484A JPH0742163B2 (en) | 1986-06-04 | 1986-06-04 | Calcareous refractory composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62288155A true JPS62288155A (en) | 1987-12-15 |
JPH0742163B2 JPH0742163B2 (en) | 1995-05-10 |
Family
ID=15035356
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61130484A Expired - Lifetime JPH0742163B2 (en) | 1986-06-04 | 1986-06-04 | Calcareous refractory composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0742163B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020071189A1 (en) * | 2018-10-02 | 2020-04-09 | 黒崎播磨株式会社 | Hot dry spraying material and method for hot dry spraying work |
-
1986
- 1986-06-04 JP JP61130484A patent/JPH0742163B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020071189A1 (en) * | 2018-10-02 | 2020-04-09 | 黒崎播磨株式会社 | Hot dry spraying material and method for hot dry spraying work |
JP2020055710A (en) * | 2018-10-02 | 2020-04-09 | 黒崎播磨株式会社 | Dry type spray material for hot working, and hot working dry type spray construction method |
Also Published As
Publication number | Publication date |
---|---|
JPH0742163B2 (en) | 1995-05-10 |
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