JPH0987065A - Urethane resin emusion coating material and refractory brick - Google Patents

Urethane resin emusion coating material and refractory brick

Info

Publication number
JPH0987065A
JPH0987065A JP7245898A JP24589895A JPH0987065A JP H0987065 A JPH0987065 A JP H0987065A JP 7245898 A JP7245898 A JP 7245898A JP 24589895 A JP24589895 A JP 24589895A JP H0987065 A JPH0987065 A JP H0987065A
Authority
JP
Japan
Prior art keywords
urethane resin
brick
coating material
coating film
film
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
Application number
JP7245898A
Other languages
Japanese (ja)
Inventor
Ichiro Aoyama
一郎 青山
Takeshi Matsumoto
松本  剛
Yoshio Kikuta
佳男 菊田
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP7245898A priority Critical patent/JPH0987065A/en
Publication of JPH0987065A publication Critical patent/JPH0987065A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/46Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
    • C04B41/48Macromolecular compounds
    • C04B41/488Other macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
    • C04B41/4884Polyurethanes; Polyisocyanates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Furnace Housings, Linings, Walls, And Ceilings (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the function of a coating film to absorb expansion of magnesia carbon brick with a relatively this coating film, by applying a specified urethane resin emulsion coating material on the surface of the brick. SOLUTION: This urethane resin emulsion coating material is prepared by compounding a urethane resin emulsion as the main component and an org. granular material which completely combusts when exposed to air at high temp. The urethane resin emulsion coating material is applied to form a coating film having <=0.8mm thickness on the surface of magnesia carbon brick to obtain refractory brick. The surface of the coating film of the obtd. refractory brick is rough and has an enough effect to prevent slipping in the process for production or building a furnace so that safeness of work can be improved. Since the org. granular material is removed by combustion during heating, the coating film can largely be shrunk in its film thickness. Thus, the thin film gives a high expansion-absorbing function.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は水性ウレタン樹脂塗
装材及び耐火煉瓦に関し、特に水性ウレタン樹脂塗装材
により塗膜を形成したマグネシアカーボン煉瓦に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a water-based urethane resin coating material and a refractory brick, and more particularly to a magnesia carbon brick having a coating film formed from the water-based urethane resin coating material.

【0002】[0002]

【従来の技術】従来、転炉、鍋等の炉体構築物に使用さ
れる耐火煉瓦としては焼成マグネシア−ドロマイト煉
瓦、マグネシアカーボン煉瓦等の塩基性耐火煉瓦が使用
されている。これらの塩基性耐火煉瓦は一般に高い熱膨
張率を持っているので、築炉後にその膨張を吸収させる
必要がある。焼成マグネシア−ドロマイト煉瓦では耐消
化性(煉瓦中のCaOに起因する粉化現象)を付与する
ためにタールを含浸させて使用され、タールを含浸させ
た後に約1mmの膜厚で表面に付着したタール層が築炉
後の膨張吸収材として利用されている。
2. Description of the Related Art Conventionally, basic refractory bricks such as calcined magnesia-domite bricks and magnesia carbon bricks have been used as refractory bricks used in furnace constructions such as converters and pots. Since these basic refractory bricks generally have a high coefficient of thermal expansion, it is necessary to absorb the expansion after furnace construction. In the case of fired magnesia-domite brick, it was used by being impregnated with tar in order to impart digestion resistance (a powdering phenomenon due to CaO in the brick), and after impregnating tar, it was adhered to the surface with a thickness of about 1 mm The tar layer is used as an expansion absorber after furnace construction.

【0003】しかしながら、焼成マグネシア−ドロマイ
ト煉瓦はマグネシアカーボン煉瓦と比べると耐用性が低
いので、今日では次第に耐用性が高いマグネシアカーボ
ン煉瓦が多用されるようになっている。通常、マグネシ
アカーボン煉瓦では耐酸化性を付与するために金属粉末
が添加されており、この金属粉末は昇熱時に煉瓦に含有
されたカーボンと反応して熱膨張の大きい物質を生成す
ることから、タールに代わる新たな塗装材が必要とされ
ている。
However, since the fired magnesia-domite brick has a lower durability as compared with the magnesia carbon brick, magnesia carbon bricks having a higher durability are used more and more today. Usually, in the magnesia carbon brick, a metal powder is added to impart oxidation resistance, and this metal powder reacts with the carbon contained in the brick at the time of heating to generate a substance having a large thermal expansion, New coating materials to replace tar are needed.

【0004】また、マグネシアカーボン煉瓦はカーボン
を多量に含有しているので、表面が滑り易く、製造時や
築炉時の安全確保のためにも滑り止め材としての塗装材
が必要とされている。膨張吸収材及び滑り止め材として
の機能を持つ塗装材としてタールをマグネシアカーボン
煉瓦に塗布することも試みられたが、カーボン含有耐火
物であるマグネシアカーボン煉瓦はタールに塗れ難く、
表裏の平面と側面とで等しい膜厚が得られないという問
題がある。
Further, since the magnesia carbon brick contains a large amount of carbon, the surface is slippery, and a coating material as an anti-slip material is required for ensuring safety during manufacturing and furnace construction. . It was also tried to apply tar to magnesia carbon brick as a coating material having a function as an expansion absorbent and a non-slip material, but the magnesia carbon brick, which is a carbon-containing refractory, is difficult to apply to tar,
There is a problem that the same film thickness cannot be obtained on the front and back planes and side surfaces.

【0005】[0005]

【発明が解決しようとする課題】そこで合成樹脂、天然
樹脂あるいはこれらの混合物を煉瓦の表面に塗布するこ
とが既に提案されているが、この場合には煉瓦の表面に
形成される膜厚が比較的小さく、0.5mm以上の膜厚
を得ることが困難である。したがって、煉瓦の材質によ
っては膨張吸収材としての機能が不十分になり、せり割
りを生ずることがある。また、膨張吸収機能を高めるた
めに、塗布乾燥後にさらに塗装材を重ね塗りして膜厚を
例えば2mm程度まで厚くすることも試みられたが、こ
の場合は塗膜層の形成に多くの手間と時間がかかる上、
吸収材過剰によって炉体傾動時に煉瓦の抜け落ちが生ず
ることがある。
Therefore, it has already been proposed to apply a synthetic resin, a natural resin or a mixture thereof to the surface of a brick. In this case, the film thickness formed on the surface of the brick is compared. It is very small and it is difficult to obtain a film thickness of 0.5 mm or more. Therefore, depending on the material of the brick, the function as an expansion absorber becomes insufficient, and cracking may occur. Further, in order to enhance the expansion and absorption function, it has been attempted to apply a coating material again after coating and drying to increase the film thickness to, for example, about 2 mm. In this case, it takes a lot of time and labor to form the coating layer. It takes time and
Brick may fall off when the furnace is tilted due to excess absorber.

【0006】また、合成樹脂の場合、溶媒として有機溶
剤が使用されたものは、有機溶剤の揮発による環境汚
染、人体への影響、引火性の点で問題がある。またエマ
ルション系の水系樹脂の場合は、上記問題は無いが、樹
脂Tgが低いと塗膜形成性は良いが塗装物を積み重ねた
場合ブロッキングを生じる。Tgを高くした場合はブロ
ッキングの点で優れているが、低温時の塗膜形成性が劣
り、塗膜形成性を上げるために造膜助剤を添加した場合
はブロッキングが生じてしまう。
Further, in the case of a synthetic resin, the one in which an organic solvent is used as a solvent has problems in environmental pollution due to volatilization of the organic solvent, influence on human body, and inflammability. Further, in the case of an emulsion-based water-based resin, the above problem does not occur, but when the resin Tg is low, the coating film forming property is good, but blocking occurs when the coated objects are stacked. When Tg is increased, it is excellent in terms of blocking, but the film-forming property at low temperature is poor, and when a film-forming auxiliary is added to improve the film-forming property, blocking occurs.

【0007】[0007]

【課題を解決するための手段】本発明者は上記の問題点
を解決する目的で鋭意検討した結果、マグネシアカーボ
ン煉瓦の表面に特定の水性ウレタン樹脂塗装材を塗布す
ることにより、比較的薄い膜厚で大きな膨張吸収機能を
発揮することができることを見いだし、本発明を完成す
るに至った。
Means for Solving the Problems As a result of intensive studies for solving the above-mentioned problems, the present inventor has found that a relatively thin film can be obtained by applying a specific water-based urethane resin coating material on the surface of magnesia carbon brick. It has been found that a large thickness can exert a large expansion and absorption function, and the present invention has been completed.

【0008】即ち本発明は次の(1)及び(2)の通り
である。 (1)水性ウレタン樹脂を主体とし、これに高温で空気
に曝されたときに完全燃焼する有機顆粒物を含有させて
得られることを特徴とする水性ウレタン樹脂塗装材。 (2)(1)記載の水性ウレタン樹脂塗装材をマグネシ
アカーボン煉瓦の表面に塗布し、厚さ0.8mm以下の
塗膜を形成させて得られることを特徴とする耐火煉瓦。
That is, the present invention is as follows (1) and (2). (1) A water-based urethane resin coating material comprising a water-based urethane resin as a main component and an organic granule that completely burns when exposed to air at a high temperature. (2) A refractory brick obtained by applying the aqueous urethane resin coating material according to (1) to the surface of a magnesia carbon brick to form a coating film having a thickness of 0.8 mm or less.

【0009】[0009]

【発明の実施の形態】本発明において、塗装材の主成分
を構成する樹脂として水性ウレタン樹脂が使用される。
水性ウレタン樹脂としては、アニオン、ノニオン、カチ
オンのいずれも使用できる。これらのブレンド物も使用
できる。水性ウレタン樹脂に用いられるイソシアネート
成分及びポリオール成分としては、公知のすべてのもの
が使用できるが、経済性の点から特に好適なものは、前
者の例としてトリレンジイソシアネート(異性体の混合
物を含む。)、ジフェニルメタンジイソシアネート(異
性体及び多核体等の混合物を含む。)等が、後者の例と
して各種のポリエーテルポリオール、ポリエステルポリ
オール等があげられる。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, an aqueous urethane resin is used as a resin constituting the main component of a coating material.
As the water-based urethane resin, any of anion, nonion and cation can be used. Blends of these can also be used. As the isocyanate component and the polyol component used in the water-based urethane resin, all known ones can be used, but from the viewpoint of economy, particularly preferable ones include tolylene diisocyanate (mixture of isomers). ), Diphenylmethane diisocyanate (including a mixture of isomers and polynuclear compounds), and the like, and examples of the latter include various polyether polyols and polyester polyols.

【0010】また、水性ウレタン樹脂とアクリルエマル
ション、酢ビエマルション等の水性または水分散タイプ
の樹脂とのブレンド物も使用できる。水性ウレタン樹脂
あるいはブレンド物に硬化剤(ウレタン、エポキシ、ア
ジリジン、カルボジイミド、メラミン樹脂等)を併用し
ても使用できる。酸化重合タイプの水性ウレタン樹脂も
勿論使用できる。また、樹脂に添加される有機顆粒物と
しては、高温で空気に曝されたときに完全燃焼するもの
であれば特に限定されず、例えば、ピッチパウダー、お
がくず等を使用することができる。
Further, a blend of an aqueous urethane resin and an aqueous or water-dispersion type resin such as an acrylic emulsion or a vinyl acetate emulsion can also be used. A curing agent (urethane, epoxy, aziridine, carbodiimide, melamine resin, etc.) can be used in combination with the aqueous urethane resin or blend. Of course, an oxidative polymerization type aqueous urethane resin can also be used. Further, the organic granules added to the resin are not particularly limited as long as they are completely combusted when exposed to air at a high temperature, and for example, pitch powder, sawdust and the like can be used.

【0011】塗膜をマグネシアカーボン煉瓦の表面に形
成する方法としては、刷毛、ローラー、ヘラ、スプレー
により塗布したり、ディッピンク等の公知の方法で液体
を煉瓦の表面に付着させて、この後、乾燥させるという
方法が採用される。この液体は水性ウレタン樹脂を主成
分としているのでカーボン含有煉瓦であるマグネシアカ
ーボン煉瓦との濡れ性もよく、かつ、塗膜形成性、乾燥
性、耐摩耗性、ブロッキング性にも優れ、煉瓦の表裏の
平面と側面との膜厚を等しくできる。
As a method for forming the coating film on the surface of the magnesia carbon brick, it is applied by a brush, a roller, a spatula or a spray, or a liquid is adhered to the surface of the brick by a known method such as dipping, and then, The method of drying is adopted. Since this liquid contains water-based urethane resin as the main component, it has good wettability with the magnesia carbon brick, which is a carbon-containing brick, and also has excellent film-forming properties, drying properties, abrasion resistance, and blocking properties. It is possible to make the film thickness of the plane and the side surface of the film uniform.

【0012】また、塗膜の膜厚は有機顆粒物の添加量を
増減することにより、0.8mm以下の範囲で自由に変
えることができる。膜厚を0.8mmよりも厚くするこ
とは技術的には可能であるが、膜厚が0.8mmを上回
ると炉体傾動時に吸収体過剰による煉瓦の抜け落ちが生
ずることが有るので好ましくない。このような塗膜を形
成した煉瓦の表面は、塗膜を有しないマグネシアカーボ
ン煉瓦の表面に比べて粗荒であり、滑り難くなってい
る。また、昇熱時には有機顆粒物が完全燃焼して除去さ
れて、塗膜の膜厚に対する収縮量が大きくなるので、薄
い膜厚で大きな膨張を吸収できる。従って、膜厚を0.
8mm以下で調整することにより材質に対応した膨張を
吸収できるようになり、膨張吸収が不十分になってせり
割れが生じたり、吸収材過剰による炉体傾動時の煉瓦の
抜け落ちが生じたりすることを防止できる。
The film thickness of the coating film can be freely changed within a range of 0.8 mm or less by increasing or decreasing the amount of organic granules added. Although it is technically possible to make the film thickness thicker than 0.8 mm, if the film thickness exceeds 0.8 mm, bricks may fall off due to excess absorber when the furnace body tilts, which is not preferable. The surface of the brick having such a coating film is rougher than the surface of the magnesia carbon brick having no coating film, and is less likely to slip. In addition, since the organic granules are completely combusted and removed during heating, and the amount of shrinkage with respect to the film thickness of the coating film increases, a large expansion can be absorbed with a thin film thickness. Therefore, the film thickness is set to 0.
By adjusting it to 8 mm or less, it will be possible to absorb the expansion corresponding to the material, expansion absorption will be insufficient and cracks will occur, or bricks will fall out when the furnace body is tilted due to excessive absorption material. Can be prevented.

【0013】[0013]

【実施例】本発明を実施例により更に具体的に説明する
が、本発明はこれらに限定されるものではない。
EXAMPLES The present invention will be described in more detail with reference to examples, but the present invention is not limited thereto.

【0014】実施例1 温度計、撹拌機、冷却管、窒素導入管を備えた2000
mlの四つ口フラスコに、分子量2000のポリプロピ
レングリコール86.5g、ネオペンチルグリコール5
3.4g、トリメチロールプロパン4.3g、ジメチロ
ールプロピオン酸17.9g、N−メチル−2−ピロリ
ドン34.5gを装入し、窒素を導入しながら90℃ま
で昇温し内容物を溶解した。次に40℃まで冷却しアセ
トン72.0gを入れ、次いでトリレンジイソシアネー
ト137.8gを1時間かけて滴下した。内温を40〜
50℃に保ち8時間反応を行った後、アセトン100.
5gで希釈した。得られたウレタンプレポリマーのNC
O基含有量は0.90%であった。
Example 1 2000 equipped with a thermometer, a stirrer, a cooling pipe, and a nitrogen introducing pipe
In a ml four-necked flask, 86.5 g of polypropylene glycol having a molecular weight of 2000 and neopentyl glycol 5
3.4 g, trimethylolpropane 4.3 g, dimethylolpropionic acid 17.9 g and N-methyl-2-pyrrolidone 34.5 g were charged, and the temperature was raised to 90 ° C. while introducing nitrogen to dissolve the contents. . Next, the mixture was cooled to 40 ° C., 72.0 g of acetone was added, and then 137.8 g of tolylene diisocyanate was added dropwise over 1 hour. Inner temperature 40 ~
After the reaction was carried out at 50 ° C. for 8 hours, acetone 100.
Diluted with 5 g. NC of the obtained urethane prepolymer
The O group content was 0.90%.

【0015】ジメチルエタノールアミン10.7gを含
有する脱イオン水504.4gを40℃に保ち、そこに
上記のウレタンプレポリマー506.9gを滴下し、水
性化及び鎖伸長反応を行い、水性ウレタン樹脂溶液を得
た。この水性ウレタン樹脂溶液を、さらに40℃で減圧
脱アセトンを行い樹脂分38.0%、PH7.6、粘度
200CP/25℃のアニオン性、自己乳化型水性ウレ
タン樹脂を得た。得られた水性ウレタン樹脂65.2g
に、顆粒状ピッチ(揮発分45〜55%、固定炭素45
〜55%、灰分1%を含有した粒度0.3mm以下が9
0%以上のもの)27.9g、おがくず(0.5mm以
下)6.9gを混合し、水性ウレタン樹脂塗装材を得
た。
504.4 g of deionized water containing 10.7 g of dimethylethanolamine was kept at 40 ° C., and 506.9 g of the above urethane prepolymer was added dropwise thereto to carry out hydration and chain extension reaction to obtain an aqueous urethane resin. A solution was obtained. This aqueous urethane resin solution was further deaerated under reduced pressure at 40 ° C. to obtain an anionic, self-emulsifying aqueous urethane resin having a resin content of 38.0%, PH 7.6, and a viscosity of 200 CP / 25 ° C. 65.2 g of the obtained aqueous urethane resin
, Granular pitch (volatile content 45-55%, fixed carbon 45
~ 55%, 1% ash content particle size 0.3mm or less 9
27.9 g (of 0% or more) and 6.9 g of sawdust (0.5 mm or less) were mixed to obtain an aqueous urethane resin coating material.

【0016】実施例2 温度計、撹拌機、冷却管、窒素導入管を備えた2000
mlの四つ口フラスコに、XP1077E(アマニ油と
ペンタエリスリトールのエステル交換ポリオール、分子
量638、沃素価133、三井東圧化学(株)製)11
5.4g、分子量2000のポリテトラメチレンエーテ
ルグリコール71.2g、トリメチロールプロパン5.
8g、ジメチロールプロピオン酸21.5g、N−メチ
ル−2−ピロリドン34.4gを装入し窒素を導入しな
がら90℃まで昇温し、内容物を溶解した。次に40℃
まで冷却し、アセトン86.5gを入れ次いでトリレン
ジイソシアネート86.2gを1時間かけて滴下した。
内温を40〜50℃に保ち8時間反応を行った後アセト
ン86.5gで希釈した。得られたウレタンプレポリマ
ーのNCO基含有量は、0.90%であった。
Example 2 2000 equipped with a thermometer, a stirrer, a cooling pipe, and a nitrogen introducing pipe
In a ml four-necked flask, XP1077E (transesterified polyol of linseed oil and pentaerythritol, molecular weight 638, iodine value 133, manufactured by Mitsui Toatsu Chemicals, Inc.) 11
5.4 g, molecular weight 2000 polytetramethylene ether glycol 71.2 g, trimethylol propane 5.
8 g, dimethylolpropionic acid 21.5 g and N-methyl-2-pyrrolidone 34.4 g were charged and the temperature was raised to 90 ° C. while introducing nitrogen to dissolve the contents. Next 40 ° C
After cooling, 86.5 g of acetone was added and then 86.2 g of tolylene diisocyanate was added dropwise over 1 hour.
The reaction was carried out for 8 hours while keeping the internal temperature at 40 to 50 ° C, and then diluted with 86.5 g of acetone. The NCO group content of the obtained urethane prepolymer was 0.90%.

【0017】ジメチルエタノールアミン12.1gを含
有した脱イオン水485.0gを50℃に保ち上記ウレ
タンプレポリマーを507.5gを滴下し、水性化及び
鎖伸長反応を行い、水性ウレタン樹脂溶液を得た。この
水性ウレタン樹脂溶液を、さらに40℃で減圧脱アセト
ンを行い樹脂分38.0%、PH7.6、粘400CP
/25℃のアニオン性、自己乳化型の酸化重合型水性ウ
レタン樹脂を得た。この水性ウレタン樹脂95.0g、
酸化重合触媒(DICNATE3111・大日本インキ
化学工業(株)製)1.8g、おがくず(0.5mm以
下)5.0gを混合し、水性ウレタン樹脂塗装材を得
た。
485.0 g of deionized water containing 12.1 g of dimethylethanolamine was kept at 50 ° C. and 507.5 g of the above urethane prepolymer was added dropwise to carry out hydration and chain extension reaction to obtain an aqueous urethane resin solution. It was This aqueous urethane resin solution was further subjected to vacuum deacetoneation at 40 ° C. to obtain a resin content of 38.0%, PH 7.6, and a viscosity of 400 CP.
An anionic, self-emulsifying, oxidative polymerization type aqueous urethane resin of / 25 ° C. was obtained. 95.0 g of this aqueous urethane resin,
An oxidation polymerization catalyst (DICNATE 3111, manufactured by Dainippon Ink and Chemicals, Inc.) (1.8 g) and sawdust (0.5 mm or less) (5.0 g) were mixed to obtain an aqueous urethane resin coating material.

【0018】実施例3 実施例1で得た水性ウレタン樹脂塗装材を成形後の転炉
用マグネシアカーボン煉瓦にローラーで約0.6mmの
厚さに塗布し、その後所定の温度で乾燥させて煉瓦表面
に塗膜を形成させ、本発明の耐火煉瓦を得た。 実施例4 実施例2で得た水性ウレタン樹脂塗装材を成形後の転炉
用マグネシアカーボン煉瓦にローラーで約0.6mmの
厚さに塗布し、その後所定の温度で乾燥させて煉瓦表面
に塗膜を形成させ、本発明の耐火煉瓦を得た。
Example 3 The water-borne urethane resin coating material obtained in Example 1 was applied to a molded magnesia carbon brick for a converter with a roller to a thickness of about 0.6 mm, and then dried at a predetermined temperature to brick. A coating film was formed on the surface to obtain the refractory brick of the present invention. Example 4 The water-based urethane resin coating material obtained in Example 2 was applied to a molded magnesia carbon brick for a converter with a roller to a thickness of about 0.6 mm, and then dried at a predetermined temperature to apply it to the brick surface. A film was formed to obtain a refractory brick of the present invention.

【0019】実施例3及び4で形成された塗膜の表面は
粗荒であり、滑り難くなっていた。得られた耐火煉瓦、
即ち塗膜で被覆されたマグネシアカーボン煉瓦を180
t転炉の絞り部に全面施工したところ、炉腹部の煉瓦の
熱膨張による突き上げ分が吸収され、従来見られたせり
割れ現象が解消されたことが確認できた。さらに、実炉
においてこの耐火煉瓦を使用したところ、内張り煉瓦の
熱膨張率の1/3相当量が塗膜によって吸収され、吸収
材過剰による炉体傾動時の煉瓦の抜け落ちもなく、せり
割れも発生しないという良好な結果が得られた。
The surfaces of the coating films formed in Examples 3 and 4 were rough and slip-resistant. Obtained refractory bricks,
That is, 180 magnesia carbon bricks coated with a coating film
When the entire area was applied to the narrowed portion of the t converter, it was confirmed that the thrust up due to the thermal expansion of the bricks in the furnace abdomen was absorbed and the conventional cracking phenomenon was eliminated. Furthermore, when this refractory brick was used in an actual furnace, the coating film absorbed 1/3 of the coefficient of thermal expansion of the lining brick, and the brick did not fall off when the furnace body was tilted due to excess absorber, and cracking did not occur. The good result that it does not occur was obtained.

【0020】[0020]

【発明の効果】以上のように本発明に使用する塗装材が
水性ウレタン樹脂を主体としているので、カーボン含有
煉瓦であるマグネシアカーボン煉瓦との濡れ性が高く、
マグネシアカーボン煉瓦の表面全体に塗膜を均等に形成
できる。また、上記塗装材が水性ウレタン樹脂を主体と
し、有機顆粒物を含有しているので煉瓦表面に形成され
る塗膜の表面が粗荒で、製造時や築炉時の滑り止めを充
分図ることができ、作業の安全性を高めることができ
る。さらに、本発明は高温で空気に曝されたときに完全
燃焼する有機顆粒物を含有した塗装材を使用しているの
で、昇熱時にこの有機顆粒物が燃焼して除去されること
により膜厚に対して大きく収縮させることができ、薄い
膜厚で大きな膨張吸収機能を発揮させることができ、せ
り割れ現象の発生を防止できると共に、塗膜の膜厚を薄
くして吸収材過剰による炉体傾動時の煉瓦の抜け落ち現
象を防止できる。加えて、本発明は塗装材の有機顆粒物
の配合割合を調整することにより塗膜の膜厚を0.8m
m以下で任意に調整できる。特に日々改良が加えられて
いるマグネシアカーボン煉瓦では材質によってその熱膨
張率が異なってくることを鑑みれば、材質の熱膨張率に
対応して膜厚を調整できる本発明は改良された種々のマ
グネシアカーボン煉瓦に対応できるから、炉寿命の延長
を図る上で極めて有用である。
As described above, since the coating material used in the present invention is mainly composed of the water-based urethane resin, the wettability with the magnesia carbon brick which is a carbon-containing brick is high,
A coating film can be uniformly formed on the entire surface of a magnesia carbon brick. Further, since the coating material is mainly composed of a water-based urethane resin and contains organic granules, the surface of the coating film formed on the brick surface is rough, and it is possible to sufficiently prevent slippage during manufacturing or furnace construction. Therefore, the safety of work can be improved. Further, since the present invention uses a coating material containing an organic granule that completely burns when exposed to air at a high temperature, the organic granule burns and is removed during heating to increase the film thickness. When the furnace body is tilted due to excess absorber, the thickness of the coating film can be reduced to prevent the occurrence of a cracking phenomenon. It is possible to prevent the phenomenon of brick falling out. In addition, according to the present invention, the film thickness of the coating film is adjusted to 0.8 m by adjusting the blending ratio of the organic granules of the coating material.
It can be arbitrarily adjusted at m or less. In particular, in view of the fact that the coefficient of thermal expansion of a magnesia carbon brick, which is improved every day, varies depending on the material, the present invention is capable of adjusting the film thickness according to the coefficient of thermal expansion of the material. Since it can be applied to carbon bricks, it is extremely useful in extending the life of the furnace.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】水性ウレタン樹脂を主体とし、これに高温
で空気に曝されたときに完全燃焼する有機顆粒物を含有
させて得られることを特徴とする水性ウレタン樹脂塗装
材。
1. A water-based urethane resin coating material comprising a water-based urethane resin as a main component, and an organic granule that completely burns when exposed to air at a high temperature.
【請求項2】請求項1記載の水性ウレタン樹脂塗装材を
マグネシアカーボン煉瓦の表面に塗布し、厚さ0.8m
m以下の塗膜を形成させて得られることを特徴とする耐
火煉瓦。
2. A water-based urethane resin coating material according to claim 1 is applied to the surface of a magnesia carbon brick to give a thickness of 0.8 m.
A refractory brick obtained by forming a coating film of m or less.
JP7245898A 1995-09-25 1995-09-25 Urethane resin emusion coating material and refractory brick Pending JPH0987065A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7245898A JPH0987065A (en) 1995-09-25 1995-09-25 Urethane resin emusion coating material and refractory brick

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7245898A JPH0987065A (en) 1995-09-25 1995-09-25 Urethane resin emusion coating material and refractory brick

Publications (1)

Publication Number Publication Date
JPH0987065A true JPH0987065A (en) 1997-03-31

Family

ID=17140467

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7245898A Pending JPH0987065A (en) 1995-09-25 1995-09-25 Urethane resin emusion coating material and refractory brick

Country Status (1)

Country Link
JP (1) JPH0987065A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100369701B1 (en) * 2000-02-11 2003-01-30 (주)알엔씨 Method for manufacturing a block using used-up urethane or rubber
JP2006233135A (en) * 2005-02-28 2006-09-07 Kurosaki Harima Corp Aqueous resin coating agent and refractory brick obtained by using the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100369701B1 (en) * 2000-02-11 2003-01-30 (주)알엔씨 Method for manufacturing a block using used-up urethane or rubber
JP2006233135A (en) * 2005-02-28 2006-09-07 Kurosaki Harima Corp Aqueous resin coating agent and refractory brick obtained by using the same

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