JPS58204866A - Manufacture of carbon-oxide refractories - Google Patents

Manufacture of carbon-oxide refractories

Info

Publication number
JPS58204866A
JPS58204866A JP57084589A JP8458982A JPS58204866A JP S58204866 A JPS58204866 A JP S58204866A JP 57084589 A JP57084589 A JP 57084589A JP 8458982 A JP8458982 A JP 8458982A JP S58204866 A JPS58204866 A JP S58204866A
Authority
JP
Japan
Prior art keywords
carbon
pitch
component
refractories
oxide
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
Application number
JP57084589A
Other languages
Japanese (ja)
Other versions
JPS6411587B2 (en
Inventor
石橋 種三
美喜夫 阪口
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.)
Harima Refractories Co Ltd
Original Assignee
Harima Refractories Co Ltd
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 Harima Refractories Co Ltd filed Critical Harima Refractories Co Ltd
Priority to JP57084589A priority Critical patent/JPS58204866A/en
Publication of JPS58204866A publication Critical patent/JPS58204866A/en
Publication of JPS6411587B2 publication Critical patent/JPS6411587B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Ceramic Products (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】 本発明は、連続鋳造用耐火物、転炉内帳り拐などに好適
な炭素−酸化物系−1人物の製造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 a carbon-oxide type-1 material suitable for continuous casting refractories, converter interior refractories, and the like.

欣索−酸化物、・糸面4火物は、炭素成分の存在VCよ
って耐スポール性および耐溶損性にすぐれた耐火物とし
て製鋼分野で多用されている。しかし、未だ完成された
ものではなく、また、最近の使用条件の苛酷化から、そ
の耐スポール性・自↑溶損性においても改善の余地が多
々残されている。
Oxides and refractories are widely used in the steel manufacturing field as refractories with excellent spall resistance and erosion resistance due to the presence of VC, a carbon component. However, it has not yet been perfected, and due to recent harsher usage conditions, there is still much room for improvement in its spall resistance and self-erosion resistance.

本発明は、これら炭素−酸化物系耐火物における上記特
性を、さらに向上すべく技術的改善を加えたものである
The present invention adds technical improvements to further improve the above characteristics of these carbon-oxide refractories.

従来、この檎の耐火物の結合剤として、ピッチおよびフ
ェノール樹脂が知られている。この結合剤は殆ど単独で
使用されており、両者を併用した場合も単に、フェノー
ル樹脂による作業性、つまり常温混練可能を意図したも
のにすぎない。
Conventionally, pitch and phenolic resin have been known as binders for this refractory material. This binder is almost always used alone, and even when both are used together, the purpose is simply to improve the workability of the phenol resin, that is, to enable kneading at room temperature.

そこで本発明者らは、ピッチおよびフェノール樹脂を炭
素−酸化物系11火物の結合剤としての性能を向上すべ
く実験を重ねた結果、その種@t−%定のものに限定す
るとともに、両者を一足の割合で併用すると、強固に緻
密なカーボシボシドを向を大物組織中に形成することを
晃い出すことができた。
Therefore, as a result of repeated experiments to improve the performance of pitch and phenol resin as binders for carbon-oxide type 11 fire materials, the present inventors limited the pitch and phenolic resin to those with a constant @t-%, and When both were used in combination, it was possible to form a strong and dense carbosiboside in the tissue of a large fish.

すなわち、本発明HBS成分40%以上、QI成分20
%以下のピッチと、数平均分子ffi(Mn)1000
以下のフェノール樹脂上を、重駄比ごツチ/フェノール
樹脂0.2〜5とした結合剤を使用することを特徴とし
た炭素−酸化物糸11大物の製造方法である。
That is, the HBS component of the present invention is 40% or more, and the QI component is 20% or more.
% or less pitch and number average molecular ffi (Mn) 1000
This is a method for producing a carbon-oxide yarn of 11 sizes, characterized in that the following phenol resin is coated with a binder having a weight ratio of 0.2 to 5 for the phenol resin.

第1図ないL第5図は、本発明を成すに至った実験結果
の一部である。
Figure 1 and Figure 5 are part of the experimental results that led to the present invention.

この実験は、結合剤として使用したピッチおよびフェノ
ール樹脂の材質とその組合せ比を変化させ、それによる
耐火物の特性変化を調べたものである。
In this experiment, we varied the materials and combination ratio of pitch and phenolic resin used as binders, and investigated the resulting changes in the properties of the refractory.

対象の耐火物は、いずれも黒鉛30 wt%、アルミナ
7Qwt%に結合剤10wt%(外掛)を必版加して混
練し、ラバーラレスにより1000h/cm”で成形し
た後、1000℃で還元焼成したものである。
The target refractories were all made by kneading 30 wt% graphite and 7 Qwt% alumina with 10 wt% binder (outer layer), forming them at 1000 h/cm'' using a rubber lathe, and then reducing and firing them at 1000°C. It is something.

第1図は、ピッチとフェノール樹脂の種類を一定にし、
その゛利金の比と、曲げ頻さとの関係を示したものであ
る。ヒ゛ソチ/フェノール樹脂の比が0.2〜5以外の
範囲でに、曲げ強さの向上が認められなく、ピッチまた
はフェノール樹脂をそれぞれ単独で使用した場合と変わ
らなくなる。
Figure 1 shows that the pitch and type of phenolic resin are constant,
This shows the relationship between the interest rate and the frequency of bending. When the ratio of pitch/phenolic resin is in a range other than 0.2 to 5, no improvement in bending strength is observed and the bending strength is no different from that when pitch or phenolic resin is used alone.

IA2図は、ピッチおよびフェノール樹脂の比を1とし
、ピッチ成分中のBS成分およびQI酸成分変化と、曲
げ強さとの関係ヲ壓すものである。ピッチのBS成分が
40%以下で、かつQI酸成分20%以上でah火物の
曲げ強さ力;不十分である。
In the IA2 diagram, the ratio of pitch and phenolic resin is set to 1, and the relationship between changes in the BS component and QI acid component in the pitch component and bending strength is investigated. If the BS component of the pitch is 40% or less and the QI acid component is 20% or more, the bending strength of the fireworks is insufficient.

なお、BS成分、Q工成分とは、ピッチ類の溶剤分別法
で最も一般的に行なわれるベシゼシを浴剤としたベシゼ
シirI溶成分(BS)、士ノリシを溶剤とした十ノリ
シネ溶成分(QI)のことである。
In addition, BS component and Q component are Beshizeshi irI solvent component (BS) using Beshizeshi as a bath agent, which is the most commonly used method for solvent fractionation of pitches, and Tenorishine solvent component (QI) using Shinorishi as a solvent. ).

一方、フェノール樹脂は第3図に示すように、数平均分
子Ill(Mn)が1000以下のものが、曲は強さに
良好な結釆會示している。
On the other hand, as shown in FIG. 3, phenolic resins with a number average molecular Ill (Mn) of 1000 or less exhibit good bonding strength and strength.

このように、ピッチとフェノール樹脂とを併用し、しか
もその材質と組合せ比とを特定の範囲VC限だすること
によって良好な強度の向上効釆か得られるのは、次の理
由によるものと考えられる。
The reason why a good strength improvement effect can be obtained by using pitch and phenolic resin in combination, and by setting the material and combination ratio within a specific VC range, is thought to be due to the following reasons. It will be done.

すなわち、じツチ単味をバインターとして使用すると、
第4図に示す流れ構造となり、船人Qlt+の焼成中あ
るいは使用中にバイジター内部に亀裂が入り、カーホシ
ボンド組織の破壊靭性が低下するため、炭素−酸化物炉
材としての強度に下がる。一方、フェノールレジシ単味
をバイジターとして使用すると、第5図に示すガラス状
構造となり、焼成中の亀裂は発生し絵いが、外力により
一度亀裂が入ると、その均−組織のため亀袋伝描抵抗性
ンご欠け、屍素−酸化物17−’Itとしての強度は低
下する。
In other words, when using Jituchi Monomi as a binder,
A flow structure is formed as shown in FIG. 4, and cracks occur inside the vigitor during firing or use of the shipman Qlt+, and the fracture toughness of the carboxy bond structure decreases, resulting in a decrease in the strength as a carbon-oxide furnace material. On the other hand, when a single phenol resin is used as a vigitator, it becomes a glass-like structure as shown in Figure 5, and cracks occur during firing, but once cracks occur due to external force, the structure becomes uniform and the structure becomes transparent. The strength of the carbon-oxide 17-'It decreases due to the cracking of the conductive resistance.

これに対し1本発明ではピッチとフェノールレジシを併
用し、その両者の比と種類を前述の如く、特定の比に限
定することで、バインターの炭化組織をt11イク?#
造ならしめ、カーホシホシドの破壊靭性ならびVこ亀裂
伝播抵抗性全回上させ、炭素−酸化物T材の強度を向上
させた。
On the other hand, in the present invention, pitch and phenol resin are used together, and the ratio and type of both are limited to a specific ratio as described above, so that the carbonized structure of the binder can be improved to t11. #
The fracture toughness and V-crack propagation resistance of carfosiphoside were improved, and the strength of carbon-oxide T material was improved.

さらに、このttJ′イクを呈するものは、組6図に示
す如く、l」−ポジ粒の集合体であるため、浸食にもす
ぐり、た特性をもつと期待できる。
Furthermore, since the material exhibiting ttJ' is an aggregate of l'-positive grains as shown in Figure 6, it can be expected to have excellent properties against erosion.

不発明で使用する炭素材は、例えば鱗状黒鉛、じツチコ
ークス、生状黒鉛などの揮発分5%以下のものが使用で
きる。一方、酸化物としては上記例のアルミナに限らず
、従来知られている酸性、中性、塩基性の耐火性金属酸
化物の中から任意のものが使用できる。
The carbon material used in the present invention may be one having a volatile content of 5% or less, such as scaly graphite, carbon coke, and raw graphite. On the other hand, the oxide is not limited to the above-mentioned alumina, but any of the conventionally known acidic, neutral, and basic refractory metal oxides can be used.

また、本発明のaf!i鍛を損なわない範囲であれは、
非酸化物系のB4C,BN%SiC%Si3N4などを
少量添加してもよい。
Moreover, the af! of the present invention! As long as it does not impair i-training,
A small amount of non-oxide type B4C, BN%SiC%Si3N4, etc. may be added.

以下、実施例を示す。Examples are shown below.

下記の表は酸化物としてアルミナとマグネシア、炭素相
としてタラファイト粒、結合剤として各種のフェノール
樹脂およびピッチを選び、これらを混練、成形(100
0”@’on2)、還元焼成(1000℃×3時間)後
、JISに従って各物性を測定した結果を示す。
The table below shows alumina and magnesia as oxides, taraphite grains as carbon phase, various phenolic resins and pitch as binders, kneading and molding (100
0''@'on2), and after reduction firing (1000° C. x 3 hours), the results of measuring each physical property according to JIS are shown.

以上のようにして得られる耐火物は、比較の従来品に比
べて高いスポーリシグ抵抗性と耐食性を示し、溶鋼によ
る熱衝撃、溶損など使用条件が特に厳しい連続鋳造用耐
火物、転炉内張り材として有用であり、高寿命炉材とし
て充分適用できるものである。
The refractories obtained in the above manner exhibit higher sporishing resistance and corrosion resistance than comparable conventional products, and are used as refractories for continuous casting and converter lining materials, which are subject to particularly severe usage conditions such as thermal shock from molten steel and melting damage. It is useful as a long-life furnace material.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はヒラ予/フェノール樹脂比と、曲げ強さの関係
を示すグラフ。 第2図はBS成分およびQI酸成分、曲は強さの関係を
示すグラフ。 wJ3図14フェノール樹脂の数平均分子皺と、曲げ強
さの関係を示すグラフ。 w、4図、第5図、第6図は図面に4(る4真でありヒ
ツチ炭化後の顕微鏡4真、倍率は300倍である。 第1図 第2図 (δ5A介)−りo    so    io    
so    b。 手お′じ補止11) 昭和nL+  〆月/θ11 1・f’l ’:力閉仔出願入 4  代  理   !、 l111II   東星都r代111区丸の内2 I’
l+ 6番2す丸の内へ重洲ヒル33゜袖     止
     誓 本願明細i中ト−Hし事項を油止いたし゛止t。 d己 1、第7頁「衣」中の第11市中(・ζ[1111スホ
一ル社]とあるを 「耐スボー1し・1土:3)」と櫨J’ 11ニラ′る
。 2、第7貞「表」中の第1欄中に 「1岨浴十り性」とめるt [1制隘]貝↑14)」とif It’−する。。 3 わ0,7  頁角艷 下1丁に [2)フェノールレジシとピッチの比Vi曹w比で(1
:l)である。」とある仄に次文。 を加入する。 r3)tsoo℃X15分→水冷グイクルで転装が観察
されたサイクル紅50 X 50 X0am 4)マグネシアル゛リボ中#鋼に対しての耐倦恒性、1
600℃XI)l浸漬後の値 比較例1の溶撰菫を100として衣7I”o11  1
1t″1 □15 ・1・ IYl’lヒth関係出願人 4  代  理  18 fi111’   東j;を都丁代111(ス丸の内2
1116番2号丸の内へ爪洲ヒル330氏名 (366
71谷山輝i、雄  5、 浦+L−iFr7督力1111 11召+11ζ7 f、  と月J′/ ++抽   
 11・、    1 本願明細書及び図面中F Ht事項を、?41IJ■−
・を二(t″t。 記 1、第8fi14〜1611目に 1第4図、第5図、・・・・・300 (iイであイ碕
、lとあるを 1 第41’Xl、第5図、第6図は、(・ずれも鯖台
削の炭化後の構造を丁イ図−〇ある。 第4図はヒ・y W ’D味の」6合の流J【輛かを/
1す。 第5図はフェノールレジク*H8の場合のカラス構造を
小−4−0 第6図は杢発!のようにヒツチとフェノ−−ルレジシを
併用した場合のtザイク栖逍を小1−o」と副止弓−る
。 2、図面中1?第4図」 1第5図」 1第6図」を別
桓の如< N] 1’t−4’ :’、)、−。 第4図 第5図 第6図
Figure 1 is a graph showing the relationship between filler/phenol resin ratio and bending strength. Figure 2 is a graph showing the relationship between the BS component and QI acid component, and the song strength. wJ3 Figure 14 Graph showing the relationship between number average molecular wrinkles of phenol resin and bending strength. w, Figure 4, Figure 5, and Figure 6 are four (4) lines in the drawings, and the microscope after carbonization is 4 lines, and the magnification is 300 times. so io
so b. Supplementary note 11) Showa nL+ 〆月/θ11 1・f'l': Force closed application entry 4 Deputy! , l111II Higashi Seito Rdai 111-ku Marunouchi 2 I'
1 + No. 6, 2, Marunouchi, Shigesu Hill, 33°, sleeves, oath, specification of the application, to-H, and the matter was closed. The 11th market (・ζ [1111 Suhorusha]) in the 7th page of ``Clothing'' in ``Ki 1'' is written as ``Tai Subo 1 Shi・1 Sat: 3)''. 2. In the 1st column of the 7th message "table", write "1 岨 Bath 14 sex" if It'-. . 3 wa 0,7 Page corner 艷 Bottom 1 cho [2] Phenol resin and pitch ratio Vi So w ratio (1
:l). ” The next sentence is faint. join. r3) tsoo°C x 15 minutes → Cycle red 50 x 50 x 0am where transfer was observed in water cooling 4) Resistance to magnesial steel, 1
Value after soaking at 600°C
1t''1 □15 ・1・IYl'lhith related applicant 4 Attorney 18 fi111'Higashij;
1116 No. 2 To Marunouchi Tsumesu Hill 330 Name (366
71 Teru Taniyama i, male 5, Ura+L-iFr7 force 1111 11 call+11ζ7 f, and moon J'/ ++ draw
11., 1 What are the F Ht matters in the specification and drawings of this application? 41IJ■-
・ 2 (t″t. Note 1, 8th fi 14-1611 1 Fig. 4, Fig. 5, ...300 (i ii de Aisaki, l 1 No. 41'Xl, Figures 5 and 6 show the structure of Sabadai after carbonization. of/
1. Figure 5 shows the crow structure in the case of Phenol Resik*H8 - Small - 4-0 Figure 6 shows heathering! As shown in the following, the effect of using a combination of hitch and phenol resin is ``1-o''. 2. 1 in the drawing? Figure 4'' 1 Figure 5'' 1 Figure 6'' are shown separately <N] 1't-4':', ), -. Figure 4 Figure 5 Figure 6

Claims (1)

【特許請求の範囲】[Claims] BS成分40%以上、QI成分20%以下のピッチと、
数平均分子1(Mn)1000以下のフェノール樹脂と
を、重敏比でピッチ/フェノール樹脂0.2〜5とした
結合剤を使1−L+することを特徴とした炭素−醪化物
系耐火物の製造方法。
A pitch with a BS component of 40% or more and a QI component of 20% or less,
A carbon-moldide-based refractory characterized in that a phenolic resin having a number average molecular weight of 1 (Mn) 1000 or less is combined with a binder having a pitch/phenol resin ratio of 0.2 to 5 to 1-L+. Production method.
JP57084589A 1982-05-19 1982-05-19 Manufacture of carbon-oxide refractories Granted JPS58204866A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57084589A JPS58204866A (en) 1982-05-19 1982-05-19 Manufacture of carbon-oxide refractories

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57084589A JPS58204866A (en) 1982-05-19 1982-05-19 Manufacture of carbon-oxide refractories

Publications (2)

Publication Number Publication Date
JPS58204866A true JPS58204866A (en) 1983-11-29
JPS6411587B2 JPS6411587B2 (en) 1989-02-27

Family

ID=13834855

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57084589A Granted JPS58204866A (en) 1982-05-19 1982-05-19 Manufacture of carbon-oxide refractories

Country Status (1)

Country Link
JP (1) JPS58204866A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53128611A (en) * 1977-04-16 1978-11-09 Kyushu Refractories Bricks bonded with carbon
JPS5688873A (en) * 1980-11-17 1981-07-18 Mitsubishi Oil Co Manufacture of carbonncontaining basic nonnburnt refractory brick
JPS6411588A (en) * 1987-07-02 1989-01-17 Yasuo Maekawa Adhesion and repairing of cover of chair

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53128611A (en) * 1977-04-16 1978-11-09 Kyushu Refractories Bricks bonded with carbon
JPS5688873A (en) * 1980-11-17 1981-07-18 Mitsubishi Oil Co Manufacture of carbonncontaining basic nonnburnt refractory brick
JPS6411588A (en) * 1987-07-02 1989-01-17 Yasuo Maekawa Adhesion and repairing of cover of chair

Also Published As

Publication number Publication date
JPS6411587B2 (en) 1989-02-27

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