JPS58185475A - Manufacture of carbonaceous refractories - Google Patents

Manufacture of carbonaceous refractories

Info

Publication number
JPS58185475A
JPS58185475A JP57069090A JP6909082A JPS58185475A JP S58185475 A JPS58185475 A JP S58185475A JP 57069090 A JP57069090 A JP 57069090A JP 6909082 A JP6909082 A JP 6909082A JP S58185475 A JPS58185475 A JP S58185475A
Authority
JP
Japan
Prior art keywords
carbon
refractory
weight
raw material
firing
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
JP57069090A
Other languages
Japanese (ja)
Inventor
多喜田 一郎
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.)
Krosaki Harima Corp
Original Assignee
Kurosaki 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 Kurosaki Refractories Co Ltd filed Critical Kurosaki Refractories Co Ltd
Priority to JP57069090A priority Critical patent/JPS58185475A/en
Publication of JPS58185475A publication Critical patent/JPS58185475A/en
Pending legal-status Critical Current

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  • Ceramic Products (AREA)
  • 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】 本発明は耐摩耗性に優れ、かつ熱膨張率の低い含炭素耐
火物の製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a carbon-containing refractory that has excellent wear resistance and a low coefficient of thermal expansion.

含炭素耐火物は優れた耐スラグ性、耐スポーリング性を
有′孝ることから、近年その使用範囲は忠速に拡大しつ
つあり、種々の酸化物原料との組み合せから成る耐火材
が実炉に供せられている。・eれらの中でイ)奄融或い
は焼結のマグネシアクリンリーとりん状黒鉛を使用した
M g O−C質れんがは電気り1.転炉、炉外製錬炉
、混銑車等の多く炉に適用され、飛躍的な炉寿命の延長
に寄与してい【)。
Since carbon-containing refractories have excellent slag resistance and spalling resistance, their range of use has been rapidly expanding in recent years, and refractory materials made from combinations with various oxide raw materials are now in production. It is offered to the furnace.・Among them, 1. It is applied to many furnaces such as converters, external smelting furnaces, and pig iron mixers, and contributes to a dramatic extension of furnace life.

般にこれらのMg0−C質れんがはコールタ−ルビ、(
、フェノール樹脂、フラン樹脂等の有機物結合剤を使用
し、500℃以下の温度で処理されたいわゆる不焼成れ
んがであるが、酸化物と本實的に結4性のない炭素結合
であるがために熱闘強度か低く、またこの炭素結合部か
りん状黒鉛にIL較し′C易酸化性である為に気相或い
はスラグ中白酸化性製造による液相酸化によって強度特
性がAL<劣化することが欠点である。
Generally, these Mg0-C bricks are made of coal tar ruby, (
It is a so-called unfired brick that is treated at a temperature below 500℃ using an organic binder such as phenolic resin or furan resin, but it is a carbon bond that does not actually bond with oxides. The hot fighting strength is low, and since this carbon bond is easily oxidized compared to IL, the strength properties may deteriorate by liquid phase oxidation due to white oxidation production in the gas phase or slag. This is a drawback.

かかるMgOC質れんがの欠点である耐酸化性、熱間強
度特性を改良する手段としてA1゜Si、Mg等のH4
酸化性金属を添加することが提案されているが、3iの
添加は耐スラグ性がやや低1−4乙軸向があり、またM
gは取扱いの危険性。
As a means to improve the oxidation resistance and hot strength characteristics, which are the drawbacks of such MgOC bricks, H4 such as A1°Si, Mg, etc.
It has been proposed to add oxidizing metals, but the addition of 3i has a slightly low slag resistance in the 1-4 axis direction, and
g is the danger of handling.

それに伴な)れんが製造時の問題があり、これらの中で
はAeが総合的に最も適すものと名えられている。。
There are problems associated with this during the manufacturing of bricks, and among these problems, Ae is said to be the most suitable overall. .

しかしながらA7!添油添加g O−C質れんがは10
00℃付近から熱膨張係数が大幅に増大すること及び残
存膨張率が増大するという大きな欠点を有しており、こ
れに起因する剥離現象いわゆる“せり割り”が実炉でし
ばしば見受けられている。
However, A7! Added oil g O-C brick is 10
It has major disadvantages in that the thermal expansion coefficient increases significantly from around 00°C and the residual expansion coefficient increases, and a peeling phenomenon caused by this, so-called "cutting", is often observed in actual furnaces.

本発明は、かかるAI添加に伴う欠点は、焼成過程で添
加したAlを炭素と反応せしめ耐火物組成中に、114
C3を生成せしめることによって解消でき、熱間強度が
高く異常膨張性のない焼成れんがが得られるという知見
に基いて完成したものである。
The present invention solves the drawbacks associated with the addition of AI by causing the added Al to react with carbon during the firing process, resulting in the addition of 114
This was completed based on the knowledge that this problem could be solved by producing C3, and a fired brick with high hot strength and no abnormal expansion could be obtained.

添加したAIと炭素質材料との焼成過程におけるAl4
C3の生成量が0.5重量%より少ない場合には、焼成
後の熱間強度が極めて低く、また例えばMg0−C質れ
んがでは焼成過程で生成するスピネル(M g O,A
 j! 203 )が耐食性の低Fをもたらすので好ま
しくない。また焼成過程においてAl4C3の生成量が
5重量%を越える場合には、焼成峙の膨張性が大きく、
れんが組織を破す′4るのC打まし、くない。したがっ
て、焼成後のAl4C3の含有量は0.5〜5重量%で
あることが姑要である。
Al4 in the firing process of added AI and carbonaceous material
If the amount of C3 produced is less than 0.5% by weight, the hot strength after firing will be extremely low, and for example, in the case of Mg0-C bricks, spinel (MgO, A
j! 203) is not preferred because it results in low F of corrosion resistance. In addition, when the amount of Al4C3 produced in the firing process exceeds 5% by weight, the expansion property during firing is large;
There is no way to break the brick structure. Therefore, it is essential that the content of Al4C3 after firing is 0.5 to 5% by weight.

4光明にト、ける耐火物Ki tlとしては、マグネジ
l′、h +1・:、ア、1【1マイ]、マグドロ、ス
ピネル、1月ミノ−、ノル:Iニア等の他に炭化珪素、
窒化珪素等のJl酸化物を挙げることができる。マグド
ロ、ムライ1、ンルコン、ンリカ等の原料は成分中4:
易Mic性のF I!203 、  F e O,C+
203 。
The refractory kits that can be used in 4 Komei include magnetic screw l', h +1.
Examples include Jl oxides such as silicon nitride. Ingredients such as Magudoro, Murai 1, Nrukong, Nrika etc. are 4 in the ingredients:
Mic-friendly FI! 203, F e O,C+
203.

:、; i (j 2を11む為、7a[共存下ではA
7!の酸化を17進し、八’4’−’3の生成を阻害す
るので好ましくない。
:,; i (j 2 is included in 11, so 7a [A in coexistence
7! This is not preferable because it inhibits the oxidation of 8′4′-′3 to the 17th base.

、した炭J2j≦c料とし′Cはりん状黒鉛、土状黒鉛
1、リーホシゾシノク、二1−クス等と使用することが
−ごきるが、天然黒鉛中には易還元性成分としζFe2
f13,5i02を含ムノテ、本発明ニ使用1−る天然
黒鉛としてはFe2O3,5i02の合量が10 dI
閂シロを越えない範囲にあるものが望ましい。耐大物原
料と炭素原料の比率は前者が50〜95重置%、後者が
5〜50%である必要かあるか1、−れはこれより炭素
原料か少ない領域では一1スラク“性、耐スポーリング
性の点で不充分であり、また50重置%より多い領域で
は酸化された場合0〕組織劣化が顕著なものとなり好ま
しくないという理由に基くものである。
, charcoal J2j≦C can be used as a material with phosphorous graphite, earthy graphite 1, leeho schizoshinoku, 21-x, etc. However, natural graphite contains easily reducible components such as ζFe2.
As the natural graphite containing f13,5i02 and used in the present invention, the total amount of Fe2O3,5i02 is 10 dI
It is desirable that it be within the range of the bar. Is it necessary that the ratio of heavy-duty materials and carbon materials be 50 to 95% for the former and 5 to 50% for the latter? This is based on the reason that the spalling property is insufficient, and that if the area is oxidized in an area of more than 50% overlap, the deterioration of the structure becomes noticeable, which is undesirable.

本発明において耐火配合物に添加する。61[粒度は、
添加する耐火原料の粒度分布に対応して任意のものを使
用するが、焼成後0.5〜511 iit %のAl1
4C3を生成するためには1重量%以Lθ)ANを添加
する必要がある。また添加AI2としくは、必ずしもA
l金属単体である必要はなく、任意金属とのAp金合金
使用でき、さらに、81およびMg等も加えて使用する
こともできる。
In the present invention it is added to fire-resistant formulations. 61 [Particle size is
Any material can be used depending on the particle size distribution of the refractory raw material to be added, but after firing, 0.5 to 511 iit% Al1
In order to produce 4C3, it is necessary to add 1% by weight or more of Lθ)AN. In addition, added AI2 does not necessarily mean A
It is not necessary to use a single metal; an Ap gold alloy with any metal can be used, and 81, Mg, etc. can also be used in addition.

本発明の耐火物の製造に当って使用するBイ〉・ダーと
しては、耐火物原料、炭素原料との濡れが良好なもので
あれば如何なるものでもよいが、Alとの反応性、炭素
結合を考慮すればJISK−2425の固定炭素測定法
において固定炭AIか20出量%を越えるもの、例えば
フェノール樹脂か望ましい。
The Bider used in the production of the refractory of the present invention may be any material as long as it has good wettability with the refractory raw material and carbon raw material. In consideration of this, it is desirable to use fixed carbon with an output of more than 20% AI, such as phenol resin, according to the JISK-2425 fixed carbon measurement method.

焼成れんがの組成中に添加AlとCとを結合さQてAl
14C3を形成させるための焼成条件に関し、では極力
酸素分圧の低い条件にする必要があり、具体的にはコー
クス中或いは不活性ガス中での焼成が+iiJ 提とな
る。焼成温度としては/l/14C3の生成量P1を加
味すれば1000℃以上が必要であり、それより低い温
度領域では/17!4C3の生成が充分でなく、不焼成
れんがと同様な異常膨張性を有4”のでIjfましくな
い。
Q by combining Al and C added during the composition of fired bricks
Regarding the firing conditions for forming 14C3, it is necessary to make the oxygen partial pressure as low as possible, and specifically, firing in coke or inert gas is recommended. The firing temperature needs to be 1000°C or higher, taking into account the production amount P1 of /l/14C3, and if the temperature is lower than that, the production of /17!4C3 will not be sufficient, resulting in abnormal expansion similar to that of unfired bricks. Since it has 4", it is not Ijf.

本発明による含炭素焼成耐火物は、従来のAllト加含
炭素質耐火物に比し、熱間強度が高く、残存膨張率の小
さいものであるが、焼成後、固定炭素の多い有機化名物
中に含浸することによって、焼成中に形成したAl14
C3の炭素結合を強化し、れんが自体の耐スポーリング
性を増大させることができる。
The carbon-containing fired refractory according to the present invention has higher hot strength and lower residual expansion coefficient than conventional all-added carbonaceous refractories, but after firing, the carbon-containing fired refractory has a large amount of fixed carbon. Al14 formed during calcination by impregnation in
It is possible to strengthen the carbon bond of C3 and increase the spalling resistance of the brick itself.

本発明の詳細な説明するために以下に比較例と共に実施
例を示す。
In order to explain the present invention in detail, examples are shown below along with comparative examples.

(実施例) 第1表に示す通り、耐火物原料として焼結マグネシア、
と電融スピネル、および炭素質原料として、りん状黒鉛
を用いて含炭素耐火物れんがを調整した。焼成後のれん
がのテスト結果から明らかな通り、比較例1に示すAl
4C3を焼成中に生成しないもの、あるいは比較例2〜
3に示すとおりAN4G、を形成しても、その形成量が
、0.5〜5.0重置%以外の焼成耐火物に対し、本発
明の範囲内にある焼成耐火物の実施例1〜5に示すもの
は、熱闘曲げ強さと熱膨張率のいずれにおいても優れた
結果を示している。
(Example) As shown in Table 1, sintered magnesia as a refractory raw material,
Carbon-containing refractory bricks were prepared using fused spinel and phosphorous graphite as the carbonaceous raw material. As is clear from the test results of the bricks after firing, the Al shown in Comparative Example 1
Those that do not generate 4C3 during firing, or Comparative Examples 2~
As shown in 3, even if AN4G is formed, the amount formed is other than 0.5 to 5.0% by weight for fired refractories, Examples 1 to 3 of fired refractories within the scope of the present invention The material shown in No. 5 shows excellent results in both hot bending strength and thermal expansion coefficient.

−ト続補正書 1.事14の表示 ■財157年 特許層 第69090号2 発明の名称 含炭素耐火物の製造法 3、  ?#正をする古 事f4との関係  特許出願人 住所 クロサキヨウギョウ 氏名 黒崎窯業賦金社 61、代理人 氏名 (8216)弁理士手掘 益 5、補■−命令の11付    昭和  年  月  
日+11  特許請求の範囲を別紙の通り訂正する。
- Continuation of amendment 1. Indication of matter 14 ■ 157th year Patent layer No. 69090 2 Name of invention Method for manufacturing carbon-containing refractories 3, ? #Relationship with ancient matters f4 to correct Patent applicant address Kurosaki Yogyo name Kurosaki Ceramics Funding Company 61, agent name (8216) Patent attorney Tegori Masu 5, Supplement ■ - Order No. 11 attached Showa year month
Day +11 The scope of claims is amended as shown in the attached sheet.

(2)明細書第2頁13行「製造」を[成分]に訂正す
る。
(2) “Manufacture” on page 2, line 13 of the specification is corrected to “component”.

(3)同第3頁14〜15行「と炭素・・・おけるJを
[の大部分が焼成過程で酸化され、結果として1に訂正
する。
(3) Ibid., page 3, lines 14-15, ``Most of J in ``and carbon...'' is oxidized during the firing process, and as a result, is corrected to 1.''

(4)同第4頁8行「マグドロ」を「マグクロ」に訂正
する。
(4) On page 4, line 8, "Magudoro" is corrected to "Magukuro".

(5)  同第4頁9行「シリカ」の後に「、クロム絋
」を加入する。
(5) Add ", chrome" after "silica" on page 4, line 9 of the same page.

(6)同第6頁16行「れんが自体の耐スポーリング性
」を1熱間強度」に訂正する。
(6) ``The spalling resistance of the brick itself'' on page 6, line 16 is corrected to ``1 hot strength''.

特6′1N求の範囲 1、耐火物II #150〜95重量%と炭素質原料5
〜50ffili !IGからなる配合物にAlあるい
は/1合金を添加し2、成形後、非酸化性雰囲気で、少
くとも100F1 ’cご焼成することを特徴とする含
炭素耐火物の製造法。
Special 6'1N required range 1, refractory II #150-95% by weight and carbonaceous raw material 5
~50ffili! 1. A method for producing a carbon-containing refractory, which comprises adding Al or /1 alloy to a compound consisting of IG, forming the compound, and then firing the mixture to at least 100F1'c in a non-oxidizing atmosphere.

2、−(火物涼料50〜95重量%と炭素質原料5〜5
0市9%からなる配合物にAlあるいはAI!合金を添
ハLIL、成形後、非酸化性雰囲気で、少くとも+00
0°(゛で焼成し、さらに、20重量%翌」P固定炭素
を含有するイj機化合物を含浸させることを特徴と−4
る含炭素耐火物の製造法。
2.-(50 to 95% by weight of fire coolant and 5 to 5% of carbonaceous raw material
Al or AI in a formulation consisting of 0% and 9%! After adding the alloy to LIL and forming, in a non-oxidizing atmosphere, at least +00
It is characterized by being calcined at 0° (゛) and further impregnated with an organic compound containing 20% by weight of P-fixed carbon.
A manufacturing method for carbon-containing refractories.

Claims (1)

【特許請求の範囲】 1、 耐火物原料50〜95電量%と炭素質原料5〜5
0重量%からなる配合物にA1を添加し、成形後、非酸
化性雰囲気で、少くともIQ 00 ゛(:で焼成する
ごとを特徴とする含炭素耐火物の製造法。 2、 耐火物原料50〜95重量%と炭素質原料5〜5
0!11量%からなる配合物にA7!を添加し、成形後
、非酸化性雰囲気で、少くとも+000°Cで焼成し、
さらに、20重量%の固定炭素を含有−4る有機化合物
を含浸させることを特徴とする含炭素耐火物の製造法。
[Scope of Claims] 1. Refractory raw material 50-95 coul% and carbonaceous raw material 5-5%
A method for producing a carbon-containing refractory, characterized in that A1 is added to a blend consisting of 0% by weight, and after molding, the mixture is fired in a non-oxidizing atmosphere to at least IQ 00゛(:). 2. A refractory raw material. 50-95% by weight and carbonaceous raw material 5-5
A7! in a formulation consisting of 0.11% by weight. After molding, bake at at least +000°C in a non-oxidizing atmosphere,
A method for producing a carbon-containing refractory, further comprising impregnating it with an organic compound containing 20% by weight of fixed carbon.
JP57069090A 1982-04-23 1982-04-23 Manufacture of carbonaceous refractories Pending JPS58185475A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57069090A JPS58185475A (en) 1982-04-23 1982-04-23 Manufacture of carbonaceous refractories

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57069090A JPS58185475A (en) 1982-04-23 1982-04-23 Manufacture of carbonaceous refractories

Publications (1)

Publication Number Publication Date
JPS58185475A true JPS58185475A (en) 1983-10-29

Family

ID=13392543

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57069090A Pending JPS58185475A (en) 1982-04-23 1982-04-23 Manufacture of carbonaceous refractories

Country Status (1)

Country Link
JP (1) JPS58185475A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50140509A (en) * 1973-12-27 1975-11-11
JPS5439422A (en) * 1977-09-02 1979-03-26 Asahi Glass Co Ltd Method of making carbonncontaining refractory having good resistance to oxidation
JPS575811A (en) * 1980-06-14 1982-01-12 Kurosaki Refract Co Ltd Refractory for upward and downward blowing converter

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50140509A (en) * 1973-12-27 1975-11-11
JPS5439422A (en) * 1977-09-02 1979-03-26 Asahi Glass Co Ltd Method of making carbonncontaining refractory having good resistance to oxidation
JPS575811A (en) * 1980-06-14 1982-01-12 Kurosaki Refract Co Ltd Refractory for upward and downward blowing converter

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