JPH03169477A - Plate brick for unburnt sliding nozzle - Google Patents
Plate brick for unburnt sliding nozzleInfo
- Publication number
- JPH03169477A JPH03169477A JP1308368A JP30836889A JPH03169477A JP H03169477 A JPH03169477 A JP H03169477A JP 1308368 A JP1308368 A JP 1308368A JP 30836889 A JP30836889 A JP 30836889A JP H03169477 A JPH03169477 A JP H03169477A
- Authority
- JP
- Japan
- Prior art keywords
- polycarbosilane
- plate brick
- weight
- oxidation
- inorganic material
- 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
- 239000011449 brick Substances 0.000 title claims abstract description 41
- 229920003257 polycarbosilane Polymers 0.000 claims abstract description 21
- 239000000843 powder Substances 0.000 claims abstract description 10
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 9
- 239000011147 inorganic material Substances 0.000 claims abstract description 9
- 239000004927 clay Substances 0.000 claims description 7
- 229920002050 silicone resin Polymers 0.000 claims description 7
- 239000005011 phenolic resin Substances 0.000 claims description 6
- 230000009970 fire resistant effect Effects 0.000 claims description 5
- 229920001187 thermosetting polymer Polymers 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 abstract description 18
- 238000007254 oxidation reaction Methods 0.000 abstract description 18
- 230000000694 effects Effects 0.000 abstract description 7
- 238000004898 kneading Methods 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 13
- 229910000831 Steel Inorganic materials 0.000 description 9
- 239000010959 steel Substances 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 230000003628 erosive effect Effects 0.000 description 5
- 230000003746 surface roughness Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000011269 tar Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229910018540 Si C Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011451 fired brick Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は製鋼工場の取鍋やタンディッシュ等に装着され
るスライディングノズル用プレートれんが(以下SNプ
レートれんがという)に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a sliding nozzle plate brick (hereinafter referred to as SN plate brick) that is installed in a ladle, tundish, etc. in a steel factory.
一般に、SNプレートれんがは、製鋼工場において取鍋
やタンディッシュの下部に装着され、溶鋼の流量の制御
に広く利用されている。Generally, SN plate bricks are installed at the bottom of ladles and tundishes in steel factories, and are widely used to control the flow rate of molten steel.
しかしながら、SNプレートれんがは、約1550〜1
600℃にもおよぶ溶融金属流による急激な熱衝撃や摩
耗等によってノズル孔部に放射状の亀裂を生じ、かかる
亀裂による溶鋼漏れの危険を招く恐れがあり、また溶融
金属流の流量制御のためにいわゆる絞り注入が常用され
るので、特に摺動面のノズル孔のエッジ部や溶融金属流
が衝突する部分が溶損され易く、このエッジ部の溶損が
原因となって、絞り注入時、あるいは注入終了後のSN
プレートれんがの摺動に伴い、溶鋼の噛み込み(いわゆ
る地金噛み込み)を生じて摺動面が次第に損耗し、いわ
ゆる摺動面荒れを生じる。However, SN plate bricks are approximately 1550-1
Radial cracks may occur in the nozzle hole due to rapid thermal shock and wear due to the molten metal flow reaching temperatures as high as 600°C, and there is a risk of molten steel leaking due to such cracks. Since so-called squeeze injection is commonly used, the edges of the nozzle hole on the sliding surface and the areas where the molten metal flow collides are particularly susceptible to melting damage. SN after injection
As the plate bricks slide, molten steel gets caught (so-called metal entrapment), and the sliding surfaces gradually wear out, resulting in so-called sliding surface roughness.
こうした状況下にあって、SNプレートれんがは溶融金
属流量の制御を司るために最も高度な機能が要求される
部位である。Under these circumstances, the SN plate brick is a part that requires the most advanced functionality in order to control the flow rate of molten metal.
一方、近年れんがの製造工程の合理化、製造コスト等の
低減のために従来よりSNプレートれんがとして使用さ
れてきたカーボンボンド焼或れんがに代わって、不焼成
SNプレートれんがが開発され、使用されつつあるが、
上記不焼威SNプレートれんがは酸化後のMi織劣化が
焼或品に比べて顕著であるため、耐酸化性を向上させる
方法が種々検討されてきた。例えば、特公昭63−32
097等で開示されたB.CやBNを添加し、酸化部で
ガラス層を形威させたものや、特公昭60−16393
で開示された炭素より酸化親和力の大きい金属アルミニ
ウム粉末を添加する、等の不焼成SNプレートれんがが
提案されている。On the other hand, in recent years, unfired SN plate bricks have been developed and are being used instead of carbon bond fired bricks, which have traditionally been used as SN plate bricks, in order to streamline the brick manufacturing process and reduce manufacturing costs. but,
Since the deterioration of the Mi weave after oxidation of the above-mentioned non-burnable SN plate bricks is more remarkable than that of burnt bricks, various methods have been investigated to improve the oxidation resistance. For example, Tokuko Sho 63-32
B. 097, etc. Those added with C or BN to form a glass layer in the oxidized part, and
Unfired SN plate bricks have been proposed in which metal aluminum powder having a higher oxidation affinity than carbon is added as disclosed in .
さらにまた、特開昭60−81068、特開昭61−1
46773等では、約500〜800℃に加熱されたS
Nプレートれんが外周部において、バインダーの炭素化
に伴い強度低下を生じ、亀裂発生や摩耗による面荒れを
生じ易いため、れんが組織の強度向上を図るためにアル
ミニウムファイバー等を添加する方法も提案されている
。Furthermore, JP-A-60-81068, JP-A-61-1
46773 etc., S heated to about 500-800℃
At the outer periphery of N-plate bricks, carbonization of the binder causes a decrease in strength, which tends to cause cracks and surface roughness due to wear, so a method of adding aluminum fibers, etc. to improve the strength of the brick structure has also been proposed. There is.
ところが、近年の製鋼コスト低減のさらなる要求に応え
て、タンディソシュを再使用することが行われるに伴い
、SNプレートれんがも同様に再使用が行われるように
なった。SNプレートれんがの再使用にあたっては、ノ
ズル孔部や摺動面に付着した地金を融解・除去するため
に酸素ジェットを吹付ける必要があり、上記ノズル孔部
や摺動面は急激な酸化作用を受ける。However, in response to the recent demand for further reduction in steel manufacturing costs, tandy sosh has been reused, and SN plate bricks have also been reused in the same way. When reusing SN plate bricks, it is necessary to spray an oxygen jet to melt and remove the base metal adhering to the nozzle holes and sliding surfaces, and the nozzle holes and sliding surfaces are subject to rapid oxidation. receive.
一般に、不焼成SNプレートれんがは酸化に伴って、含
有するカーボン或分が消失、すなわち脱炭されるとその
部分が脆弱化し、溶損や摩耗が顕著になり、耐用性が著
しく低下するという欠点や、約500〜800℃に加熱
された部分ではバインダーの炭素化に伴い強度低下を生
じ、熱応力による亀裂発生や地金付着を生じやすいとい
う欠点がある。Generally, when unfired SN plate bricks undergo oxidation, some of the carbon they contain disappears, or in other words, when they are decarburized, that part becomes brittle, becomes more susceptible to melting and wear, and its durability is significantly reduced. Also, in the portion heated to about 500 to 800° C., strength decreases due to carbonization of the binder, and there is a drawback that cracks and base metal adhesion due to thermal stress are likely to occur.
この発明は上記従来の事情に鑑みて提案されたものであ
って、不焼成SNプレートれんがの耐酸化性の向上によ
って耐用性の向上を図ることを目的としたものである。This invention has been proposed in view of the above-mentioned conventional circumstances, and is aimed at improving the durability of unfired SN plate bricks by improving their oxidation resistance.
上記課題を解決するために、この発明は以下の手段を採
用している。すなわち、耐火性無機材料からなる坏土に
対し、粒径0.2mm以下のポリカルボシランを外掛け
1〜10重量%添加するか、または上記坏土に対し、ポ
リカルボシラン溶液をポリカルボシラン量として外掛け
1〜10重量%添加し、その際に熱硬化性シリコーン樹
脂溶液、フェノールレジン、タール等とも併用すること
も可とする不焼成スライディングノズル用プレートれん
がである。In order to solve the above problems, the present invention employs the following means. That is, 1 to 10% by weight of polycarbosilane with a particle size of 0.2 mm or less is added to the clay made of a fire-resistant inorganic material, or a polycarbosilane solution is added to the clay. This is a plate brick for an unfired sliding nozzle which is added in an amount of 1 to 10% by weight and can also be used in combination with a thermosetting silicone resin solution, phenol resin, tar, etc.
本発明に使用するポリカルボシランは次式に一例を示す
ように分子内に主としてSt−C骨格構造を有する有機
珪素樹脂である。The polycarbosilane used in the present invention is an organosilicon resin mainly having an St--C skeleton structure within the molecule, as exemplified by the following formula.
ここで、Rl , R2は水素、メチル、フェニル基等
の有機官能基を示し、nは重合度を示す係数である。Here, Rl and R2 represent organic functional groups such as hydrogen, methyl, and phenyl groups, and n is a coefficient representing the degree of polymerization.
添加したポリカルボシラン、シリコーン樹脂はれんが使
用時の400〜800℃において側鎖のメチル基等の熱
分解による脱メタン反応等を生じてSiCを生威し、3
次元的なSi−C結合によってれんが組織の結合力を高
め、れんがの強度向上に寄与する。さらに高熱にさらさ
れる摺動面やノズル孔部では、酸化されてSin.を生
威し、酸化層を緻密化しカーボンの酸化を抑制する効果
を生じる。The added polycarbosilane and silicone resin cause a demethanization reaction due to thermal decomposition of the methyl groups in the side chain at 400 to 800 °C when the brick is used, producing SiC.
The dimensional Si-C bond increases the bonding strength of the brick structure and contributes to improving the strength of the brick. Furthermore, sliding surfaces and nozzle holes that are exposed to high heat are oxidized and cause Sin. This produces the effect of suppressing carbon oxidation by densifying the oxidized layer and suppressing carbon oxidation.
添加するポリカルボシランが粉末の場合には粒径が0.
2mm以下が好ましく、0.2mmより大きいとれんが
中での均一性に欠け、酸化抑制作用が低下する。また、
その添加量は1〜10重量%が適当であり、1重量%未
満であると充分な効果が得られず、IO重量%を超える
と、酸化時のれんが組織の劣化が顕著になり、耐酸化性
ならびに耐摩耗性が低下するので好ましくない。When the polycarbosilane to be added is a powder, the particle size is 0.
The thickness is preferably 2 mm or less; if it is larger than 0.2 mm, uniformity within the brick will be lacking and the oxidation inhibiting effect will be reduced. Also,
The appropriate amount of addition is 1 to 10% by weight; if it is less than 1% by weight, a sufficient effect will not be obtained, and if it exceeds IO weight%, the deterioration of the brick structure during oxidation will be significant, and the oxidation resistance will be reduced. This is not preferable because it reduces the properties and abrasion resistance.
添加するポリカルボシランが溶液の場合には、溶液中に
含有される樹脂量としては1〜10重量%が好ましく、
1重量%未満であると充分な効果が得られず、10重量
%を超えると、バインダー量過多になり、混練作業性の
低下ならびにれんがの機械的強度の低下を生じるので好
ましくない。When the polycarbosilane to be added is in the form of a solution, the amount of resin contained in the solution is preferably 1 to 10% by weight,
If it is less than 1% by weight, a sufficient effect cannot be obtained, and if it exceeds 10% by weight, the amount of binder becomes excessive, resulting in a decrease in kneading workability and a decrease in the mechanical strength of the bricks, which is not preferable.
ポリカルボシラン溶液を熱硬化性シリコーン樹脂溶液、
フェノールレジン、タール等と併用する場合には添加総
量が耐火性無機材料に対して2〜15重量%が好ましく
、2重量%未満であると充分な効果が得られず、15重
量%を超えると、バインダー量過多になり、混練作業性
の低下ならびにれんがの機械的強度の低下を生じるので
好ましくない。Polycarbosilane solution and thermosetting silicone resin solution,
When used in combination with phenol resin, tar, etc., the total amount added is preferably 2 to 15% by weight based on the fire-resistant inorganic material; if it is less than 2% by weight, sufficient effects cannot be obtained, and if it exceeds 15% by weight, This is not preferable because the amount of binder becomes too large, resulting in a decrease in kneading workability and a decrease in the mechanical strength of the bricks.
次に本発明を実施例により具体的に説明するが、本発明
はこれらの実施例に限定されるものではない。EXAMPLES Next, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples.
本発明のれんがの配合割合を第1表の上欄に示す。The blending ratio of the bricks of the present invention is shown in the upper column of Table 1.
実施例1〜3はポリカルボシラン粉末を耐火性無機材料
の微粉と予め万能ミキサーを用いて混合した後に混練・
戊形を行った。また、バインダーとして、タール、フェ
ノールレジン液体を単独または併用して添加・混練を行
った。In Examples 1 to 3, polycarbosilane powder was mixed with fine powder of a refractory inorganic material in advance using an all-purpose mixer, and then kneaded and mixed.
Performed the bogata. Further, as a binder, tar and phenol resin liquid were added and kneaded singly or in combination.
また、実施例4〜8は粒径1m1以下のポリカルボシラ
ン粉末60重量部をキシレン40重量部に溶解して作製
したポリカルポシラン溶液を添加したものであり、熱硬
化性シリコーン樹脂溶液、フェノールレジン、タール等
と併用する場合は上記ポリカルポシラン溶液と予め混合
してから耐火性無機材料に添加・混練を行った。Further, in Examples 4 to 8, a polycarposilane solution prepared by dissolving 60 parts by weight of polycarbosilane powder with a particle size of 1 m1 or less in 40 parts by weight of xylene was added, and a thermosetting silicone resin solution, a phenol When used in combination with resin, tar, etc., the mixture was mixed with the above polycarposilane solution in advance and then added to and kneaded with the refractory inorganic material.
なお、戒形時のラミネーションを防止するために、10
0℃に保持した熱風式乾燥器中で加熱処理を行い、坏土
の揮発分が第1表に示す値になるようにした。上記乾燥
処理温度はタールを添加した坏土では100℃、その他
は60℃とした。In addition, in order to prevent lamination during precepts, 10
Heat treatment was performed in a hot air dryer maintained at 0° C. so that the volatile content of the clay reached the values shown in Table 1. The drying temperature was 100°C for the tar-added clay and 60°C for the others.
戒形はフリクションプレスを用いてタンディッシュ用S
Nプレートれんがを或形した。素地は、タールを添加し
たものではコークスブリーズ中で400℃で10hr、
その他のものは空気中で180℃で24hr加熱処理し
た。The command form is S for tundish using a friction press.
N-plate bricks were shaped. If the base material is tar-added, it is heated in a coke breeze at 400℃ for 10 hours.
Others were heat treated in air at 180°C for 24 hours.
このようにして作製したSNプレートれんがの品質特性
を第1表の中欄に示す。The quality characteristics of the SN plate bricks produced in this manner are shown in the middle column of Table 1.
実施例1〜8の結果より、ポリカルポシラン粉末または
同溶液の添加によって耐酸化性が向上することがわかる
。The results of Examples 1 to 8 show that the oxidation resistance is improved by adding polycarposilane powder or its solution.
なお上記品質特性値は耐火物に対する通常法により、以
下の要領で測定した。The above quality characteristic values were measured in the following manner using the usual method for refractories.
■酸化層の厚さ:試作れんがより30x30x30 1
11の試片を各2個切出し、800℃に保持した空気雰
囲気の電気炉内に試片を入れ3hr加熱処理を行った。■Thickness of oxide layer: 30x30x30 from the prototype brick 1
Two specimens of each of No. 11 were cut out, and the specimens were placed in an electric furnace in an air atmosphere maintained at 800° C. and heat treated for 3 hours.
酸化層の厚さは加熱試験時の高さ中央部の切断面の酸化
層の厚さで示した。The thickness of the oxidized layer is indicated by the thickness of the oxidized layer at the cut surface at the center of the height during the heating test.
■溶鋼侵食指数:高周波炉に試料を内張リして1650
℃で3時間の溶鋼侵食試験を行った後、試料の中央部を
長手方向に切断し、切断面における侵食面積を測定し、
比較例1に対する相対値で示した。■ Molten steel erosion index: 1650 when the sample is lined in a high frequency furnace
After carrying out a molten steel erosion test at ℃ for 3 hours, the central part of the sample was cut in the longitudinal direction, and the erosion area on the cut surface was measured.
It is shown as a relative value to Comparative Example 1.
次に、比較例1、2、実施例1〜8のれんが各3セット
をタンディソシュ用SNプレートれんがとして実機使用
した。実機使用に当たって、溶鋼鍋1回分(約280ト
ン)のモールドへの注入を1チャージ(以下、chと略
称)として6ch連続注入した後、スラグの排出、酸素
ジェットによるノズル孔部の洗浄を行い、さらに連[6
chの鋳込みを行った(合計1 2ch鋳込み)。使用
後品を回収し観察を行った結果、第1表の下欄に示す損
傷状態であった。ポリカルボシラン粉末の添加や、バイ
ンダーとしてポリカルボシラン溶液を単独または熱硬化
性シリコーン樹脂、フェノールレジンあるいはタールと
併用添加することによってSNプレートれんが摺動面の
酸化が減少し面荒れが著しく減少した。なお、ポリ力ル
ポシランの添加によってノズル孔の溶損が若干大きくな
る傾向を示したが、溶損量は小さく、実際上問題になら
なかった。また、亀裂発生状態はいずれの場合も比較的
小さく、SNプレートれんがの廃却原因にはならなかっ
た。Next, three sets each of the bricks of Comparative Examples 1 and 2 and Examples 1 to 8 were actually used as SN plate bricks for Tandi Sosh. When using the actual machine, one charge (hereinafter referred to as "ch") of molten steel ladle (approximately 280 tons) was continuously injected into the mold through 6 channels, and then the slag was discharged and the nozzle hole was cleaned with an oxygen jet. Further series [6
Channel casting was performed (total 12 channel casting). As a result of collecting and observing the used product, it was found that the product was damaged as shown in the lower column of Table 1. By adding polycarbosilane powder and adding polycarbosilane solution as a binder alone or in combination with thermosetting silicone resin, phenol resin, or tar, oxidation of the sliding surface of SN plate bricks was reduced and surface roughness was significantly reduced. . Although the addition of polysilane tended to slightly increase the erosion loss of the nozzle hole, the amount of erosion was small and did not pose a problem in practice. In addition, the occurrence of cracks was relatively small in all cases, and did not cause the SN plate bricks to be discarded.
このように、ポリカルボシランの添加によって耐酸化性
を向上することができ摺動面の酸化による脆弱化を防ぎ
、地金噛み込みを抑制し、面荒れの低減を図ることがで
きた。In this way, the addition of polycarbosilane made it possible to improve the oxidation resistance, prevent the sliding surface from becoming brittle due to oxidation, suppress metal entrapment, and reduce surface roughness.
く以下余白〉
〔本発明の効果〕
以上のように、本発明の不焼成SNプレートれんがは従
来の炭素含有不焼成材質にポリカルボシラン粉末の添加
や、バインダーとしてポリカルボシラン溶液を単独また
は熱硬化性シリコーン樹脂溶液、フェノールレジン、タ
ール等と併用添加することによって、摺動面の酸化を抑
制し面荒れの低減を図ることができ、再使用可能な程度
に耐用性が高められる効果が得られた。[Effects of the present invention] As described above, the unfired SN plate brick of the present invention can be produced by adding polycarbosilane powder to the conventional carbon-containing unfired material, or by adding a polycarbosilane solution as a binder alone or by heat treatment. By adding it in combination with a curable silicone resin solution, phenol resin, tar, etc., it is possible to suppress oxidation of the sliding surface and reduce surface roughness, resulting in the effect of increasing durability to the extent that it can be reused. It was done.
Claims (3)
1mm以下のポリカルボシラン粉末を外掛け1〜10重
量%添加することを特徴とする不焼成スライディングノ
ズル用プレートれんが。(1) Particle size of 0.2 for clay made of fire-resistant inorganic material
A plate brick for an unfired sliding nozzle, characterized in that an outer layer of polycarbosilane powder of 1 mm or less is added in an amount of 1 to 10% by weight.
シラン溶液をポリカルボシラン量として外掛け1〜10
重量%添加することを特徴とする不焼成スライディング
ノズル用プレートれんが。(2) Add a polycarbosilane solution to the clay made of a fire-resistant inorganic material and apply the polycarbosilane amount to 1 to 10.
A plate brick for an unfired sliding nozzle characterized by adding % by weight.
シラン溶液を熱硬化性シリコーン樹脂溶液、フェノール
レジン、タール等と併用して、ポリカルボシラン量とし
て外掛け1〜10重量%添加することを特徴とする不焼
成スライディングノズル用プレートれんが。(3) Adding a polycarbosilane solution in combination with a thermosetting silicone resin solution, phenol resin, tar, etc. to clay made of a fire-resistant inorganic material in an amount of 1 to 10% by weight as an external amount of polycarbosilane. A plate brick for an unfired sliding nozzle, which is characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308368A JPH03169477A (en) | 1989-11-28 | 1989-11-28 | Plate brick for unburnt sliding nozzle |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1308368A JPH03169477A (en) | 1989-11-28 | 1989-11-28 | Plate brick for unburnt sliding nozzle |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03169477A true JPH03169477A (en) | 1991-07-23 |
Family
ID=17980227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1308368A Pending JPH03169477A (en) | 1989-11-28 | 1989-11-28 | Plate brick for unburnt sliding nozzle |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03169477A (en) |
-
1989
- 1989-11-28 JP JP1308368A patent/JPH03169477A/en active Pending
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