JPS5953555A - Oxidation preventing paint composition - Google Patents
Oxidation preventing paint compositionInfo
- Publication number
- JPS5953555A JPS5953555A JP16362982A JP16362982A JPS5953555A JP S5953555 A JPS5953555 A JP S5953555A JP 16362982 A JP16362982 A JP 16362982A JP 16362982 A JP16362982 A JP 16362982A JP S5953555 A JPS5953555 A JP S5953555A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- borax
- mixing
- coating
- weight
- 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
Landscapes
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Paints Or Removers (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、耐火物、特に黒鉛系耐火物に塗布披瀝するこ
とにより高熱に対する耐火物の酸化を防止するfB1m
組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention provides fB1m, which prevents oxidation of refractories against high heat by coating them on refractories, especially graphite refractories.
The present invention relates to a composition.
従来より黒鉛系の耐火物は、耐スポール性、耐食性に慌
れているので、製鋼の連続鋳造法において、多用されて
いる反面黒鉛系の耐火物は、重軽な組成物である黒鉛が
高熱でrIlp化、劣化することにより耐火物の目的で
ある機能に対して名曲のトラブルを生じる欠点があった
。従って、黒鉛系耐火物の酸化を防止する目的で各種の
1→ρ化防止材が、提案されているが、最も多用されて
いるものの一つに、ケイ1没アルカリ−ポウ砂系組成物
がある。Conventionally, graphite-based refractories have been widely used in continuous casting methods for steelmaking due to their spalling resistance and corrosion resistance. It has the drawback that it becomes rIlp and deteriorates, causing problems with the refractory's intended function. Therefore, various 1→ρ conversion prevention materials have been proposed for the purpose of preventing oxidation of graphite-based refractories, but one of the most widely used is a silica-based alkali-porous sand composition. be.
しかし黒鉛系耐火物が酸化する温度範囲は、約500°
C〜900°Cてありこのうち著しく酸イヒするのは、
600°C〜800°Cであるにもかかわらず、ケイ酸
アルカリ−ホウ砂系組成物の融点は、750°C以上で
あるため酸化防止効果は実・d上充分でない。また、ケ
イ酸アルカリ−ホウ砂系組成物では、組成物の安定性改
良のために、アルカリ性物質(たと、tば、N a O
tf、K OHナト) ヲ% jjk +。However, the temperature range at which graphite-based refractories oxidize is approximately 500°.
C to 900°C, and among these, the ones that are most acidic are:
Although the melting point is 600°C to 800°C, the melting point of the alkali silicate-borax composition is 750°C or higher, so the antioxidant effect is not actually sufficient. In addition, in alkali silicate-borax compositions, an alkaline substance (such as NaO) is added to improve the stability of the composition.
tf, K OH nato) wo% jjk +.
配合しており、耐水性、耐湿娃、耐久性が著しく劣り、
従ってケイ醒アルカリーホウ砂系組成物の塗膜は長期間
維持されることが那く、流失か、欠落などの被覆欠損を
起こし、醒化防山効果を、減少させている。The water resistance, moisture resistance, and durability are significantly inferior.
Therefore, the coating film of the silicified alkaline borax-based composition is not maintained for a long period of time, causing coating defects such as washing away or chipping, which reduces the silicified mountain protection effect.
本発明者らは、に記の欠点を改j勺するため鋭4Ur研
究を進めj、:結果本発明を完成したものである。The present inventors have carried out intensive research on 4Ur in order to overcome the drawbacks described below, and have completed the present invention as a result.
+jllら本発明は、ケイ酸アルカリ、ホウ砂、および
ケイY’t5 LK’f化合吻がらlfる結合ハ11に
、酸化コバルトと、アルミナなどの両性金属酸化物とを
混合し、これに0νI良を形成するに必すノな充填剤、
添加剤なとを配合して塗ネ)1伏にst’J・1゛〃シ
たことを特徴とするものである。パkに本発明の構成を
以下、fig刷11に説明する。。In the present invention, cobalt oxide and an amphoteric metal oxide such as alumina are mixed with alkali silicate, borax, and a silica Y't5 LK'f compound proboscis, and cobalt oxide and an amphoteric metal oxide such as alumina are mixed with this. A filler that is essential for forming a good quality.
It is characterized in that it contains additives and is coated with st'J. The configuration of the present invention will be explained below with reference to FIG. 11. .
本発明の構成のうち、結合イ11の一つとして最も重要
な役割を果すケイ酸鉛化合物の第1の目的は、f羊水の
ケイ酸アルカリ−ホウ砂系の組成物の融点が、750°
C以上であることに対して、61J(点を効果的に低下
させるものである。本発明においては、P l)0/
Si 02 (7)重量比が、60〜93:4゜〜7に
なるケイ酸鉛化合物を使用する。上記の範囲のケイjt
り鉛化合物は、鉛丹”4IIどの鉛化合物の喝合のよう
なtgIIl/I!時の酸化鉛ヒユームの発生が著しく
少なく、重化鉛成分の111失が、少ないばかりではな
く、環境上安全性が1%い。本発明において、重[,1
比で含有する混合物を溶解し、冷却し合ハ(シだケ、(
11,jy(、q′I化合物を、ケイ閏アルカリニホウ
砂−] Ofl : 80〜6oとなる重トd比でン1
尼合させた混合物100 %ijt部に対して6〜90
重量部好ましくけ、15〜30−rlj1部混合スル。Among the components of the present invention, the first purpose of the lead silicate compound, which plays the most important role as one of the bonds 11, is that the melting point of the amniotic fluid alkali silicate-borax composition is 750°
C or higher, 61J (effectively lowers the score. In the present invention, P l) 0/
A lead silicate compound having a weight ratio of Si 02 (7) of 60 to 93:4 to 7 is used. Key in the above range
The lead compound produces significantly less lead oxide fume during tgIIl/I!, which is the case with other lead compounds, and not only has less loss of 111 of the heavy lead component, but it is also environmentally safe. In the present invention, the weight [,1
The mixture containing the following ratio is dissolved and cooled.
11.
6 to 90 parts per 100% ijt of the amalgamated mixture
Parts by weight preferably, mixed with 1 part of 15-30-rlj.
P l+ 0 : S +02 = (50〜93:4
0〜7となるケイr憎沿化合物か、にi1己のケイrl
&アルカリーポウ1沙ン艶f¥物1゜0部に対して6部
以下においては、+;4;It点降下が5・10著でな
く醇化19′i止効果が期待できない。−万門)0:s
自)2=60〜9B:40〜7となるケイ酸鉛化合物が
」1記のケイ酸アルカリ−ポウ砂、、g 合物100部
に対して90fi量部を越えると高熱雰囲気中において
り、[1成物に過度の流動性が生じ、被膜が耐火物表面
より流失するため酸化防出の役1」が失なわれる。本発
明(7)P t+ O: S r 02 = 60〜9
3:40〜7となる
ケイ酸鉛化合物を目己合する第2の目的は次の通りテア
ル。T’l+O:5i02 =60〜93:40〜7と
なるケイ酸鉛化合物を配合した組成物は、従来のケイ酸
アルカリ−ホウ砂系組成物に、多量に配合されているア
ルカリ性物質(たとえばNa01(、KOI(など)の
使用を著しく減量させることが可能となる。本発明の構
成に基いて、規定された組合せ範囲内にあるケイ酸鉛化
合物をケイ酸アルカリニホウ砂=100 : 80〜6
0となる混合物100重量部に対して6〜90重臘部配
合して使用した場合、従来のケイ酸アルカリ−ホウ砂系
の単純な系組成物に比較してアルカリ性物質(例えば、
N a Oi4、KOHなど)の少量の添加にもかかイ
)らず、貯蔵安定性が4αめで良好で粘度上昇、分離、
ゲル化をもたらすことが全くなく、通常の環境温度(1
0°C〜40°C)下で、低粘度を維持する(1000
cps〜300CICIIS)ことができるので、塗布
施工の際の作業性が著しく良好である。また、本発明の
構成による組成物は、従来のケイ酸アルカリ−ホウ砂系
組成物に比較して、被+1’Aの耐ttL性、耐久性が
極めて向上しているため被膜形成後の長期放1置に対し
て劣化が少なく、従来のケイ酸アルカリ−ポウ砂系組成
物のような被膜の剥れ欠落を起さず長期間に亘り安定し
た状態を保持し、酸化防止の効果を常に期待できる。Pl+0:S+02=(50~93:4
Is it a compound of 0 to 7?
When the alkaline powder is 6 parts or less per 1°0 parts of the material, the drop in the point is not 5.10, and no effect on stopping 19'i of liquefaction can be expected. - Manmon) 0:s
If the lead silicate compound with 2=60-9B:40-7 exceeds 90 parts of silicic acid alkali-porous sand described in 1. [1] Excessive fluidity occurs in the component, and the coating is washed away from the surface of the refractory, so the oxidation prevention role 1 is lost. Present invention (7) P t+ O: S r 02 = 60-9
The second purpose of combining lead silicate compounds with a ratio of 3:40 to 7 is as follows. A composition containing a lead silicate compound with T'l+O:5i02 =60-93:40-7 is a composition containing a large amount of an alkaline substance (for example, Na01 (, KOI (etc.)) can be significantly reduced. Based on the structure of the present invention, lead silicate compounds within the specified combination range can be mixed into alkaline borax silicate = 100: 80 to 6.
When 6 to 90 parts by weight are added to 100 parts by weight of a mixture that gives a
Despite the addition of small amounts of NaOi4, KOH, etc.), the storage stability is good at around 4α, and there is no increase in viscosity, separation,
It does not cause gelation at all and can be used at normal ambient temperatures (1.
Maintains low viscosity (1000°C to 40°C)
cps ~ 300 CICIIS), so the workability during coating is extremely good. In addition, the composition according to the present invention has significantly improved ttL resistance and durability for +1'A coating compared to conventional alkali silicate-borax compositions, so it can be used for a long period of time after film formation. It shows little deterioration when left unattended, and maintains a stable state over a long period of time without peeling off the film like conventional alkali silicate-porous sand compositions, and maintains its antioxidant effect at all times. You can expect it.
本発明のPbO: S 1o2=6Q〜93 : 40
〜7となるケイ酸鉛化合物をケイ咽アルカリーホウ砂=
100:80〜60重量部となる混合物100重量部に
対して6〜90重量部配合した組成物の第3の目的は次
の通りである。従来のケイ酸アルカリ−ホウ砂系の組成
物は高熱が接触すると被膜中より気泡を発生するが、被
膜の必要且つ充分な流動性が不足しているため、ピンホ
ール等を形成して被膜の欠陥となる。これに反して、本
発明の構成に基ずく様にケイ酸鉛化合物を、ケイ酸アル
カリニホウ砂=to o : 3o〜60となる重量比
で混合された混合物100重量部に対して6〜90重量
部好ましくは、15〜30重量部混合する組成物におい
ては、両性金属の酸化物(たとえば、Al2O8、F
620 g す(!: ) ヲ混在すセることにより、
従来のケイ酸アルカリ−ホウ砂系、組成物にない消泡性
が得られ、高熱に曝されて被膜に発生しようとする気泡
を速かに消誠させ、ピンポールを解消して全面均一で充
分な酸化防出効果が発揮される1、
本発明の構成を、実施例、比較例により次に示すか、こ
れにより、本発明の秀れた効果が理解できるであろう。PbO of the present invention: S 1o2 = 6Q ~ 93: 40
〜7 lead silicate compound with silica alkaline borax =
The third purpose of the composition, which is blended in an amount of 6 to 90 parts by weight to 100 parts by weight of a mixture of 100:80 to 60 parts by weight, is as follows. Conventional alkali silicate-borax-based compositions generate bubbles from within the film when exposed to high heat, but because the film lacks the necessary and sufficient fluidity, pinholes are formed and the film deteriorates. It becomes a defect. On the other hand, based on the structure of the present invention, a lead silicate compound is mixed at a weight ratio of 6 to 90 parts by weight with respect to 100 parts by weight of the mixture such that the alkali silicate diborax = to o: 3 to 60. Preferably, 15 to 30 parts by weight of an amphoteric metal oxide (for example, Al2O8, F
By mixing 620 g (!: ),
It has antifoaming properties that are not found in conventional alkali silicate-borax compositions, and quickly eliminates bubbles that tend to occur in the film when exposed to high heat, eliminating pinholes and providing a uniform coating over the entire surface. 1. The structure of the present invention will be shown below with reference to Examples and Comparative Examples, which will help you understand the excellent effects of the present invention.
以下の試隔方法は下記の通りである。The spacing method below is as follows.
A。組成物の性状試験
(1)塗布作業性
各温度における塗布作業性を判定する
(2)貯蔵安定性
20°C160%RIfの室内に3ケ月間密封放置し安
定性を目視判定する
13゜被膜の性能試験
各組成物を黒鉛系耐火物の基材に500 mpの厚さで
塗布し80’Cにて4時間乾燥して被膜を形成したもの
を試験体とする。A. Property test of the composition (1) Coating workability Determining the coating workability at each temperature (2) Storage stability The stability of the 13° film was visually determined by leaving it sealed in a room at 20°C and 160% RIF for 3 months. Performance Test Each composition was applied to a graphite-based refractory base material to a thickness of 500 mp and dried at 80'C for 4 hours to form a film, which was used as a test specimen.
(1)被膜の耐久性
20°C180%R1−Tの恒温、恒湿室内に試験体を
2ケ月間、静置し、その後被膜表面を観察して耐久性を
目視判定する。(1) Durability of Coating The test specimen was left standing in a constant temperature and humidity chamber at 20° C. 180% R1-T for two months, and then the coating surface was observed to visually determine the durability.
(2)被膜の酸化防止性
添付図面に示す温度曲線に基すいて」−昇する炉内温度
のガス炉(、I= P (3カス)内に4時間収容した
後取り出し、常温まで急冷して基材の酸化程度を目視判
定する。(2) Anti-oxidation properties of the coating Based on the temperature curve shown in the attached drawing, the film was stored in a gas furnace (I = P (3 slag) for 4 hours at an increasing internal temperature, then taken out and rapidly cooled to room temperature. Visually judge the degree of oxidation of the base material.
※、Pl)0:5i02=85: 1’5結果 判定、◎優、○秀、△問題あり、×不可*, Pl) 0:5i02=85:1’5 result Judgment: ◎Excellent, ○Excellent, △Problems, ×Not possible
図は酸化防止性試験を行うカス炉内の温度変化を示すも
のである。
477−The figure shows the temperature change inside the slag furnace in which the anti-oxidation test was conducted. 477-
Claims (1)
らなる結合剤に、酸化コバルトとアルミナなどの11J
d性金属酸化物とを混合し、こ第1に被膜を形成するに
必要な充項剤、添加剤などを配合して塗4;9↓状に調
整したことを特徴とする酸化防止被覆組成物。 26ケイ酸沿化合物において、J)bO/5i02の重
量化を60〜93:40〜7の範囲に規定することを特
徴とする特許請求の範囲1記載の酸化防止被覆組成物[Claims] l. 11J such as cobalt oxide and alumina to a binder consisting of alkali silicate, borax, and lead silicate compound.
An oxidation-preventing coating composition characterized in that it is prepared by mixing a d-type metal oxide and firstly adding fillers, additives, etc. necessary for forming a coating to form a coating of 4:9↓. thing. The antioxidant coating composition according to claim 1, characterized in that in the 26 silicic acid compound, the weight ratio of J) bO/5i02 is defined in the range of 60 to 93:40 to 7.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16362982A JPS5953555A (en) | 1982-09-20 | 1982-09-20 | Oxidation preventing paint composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16362982A JPS5953555A (en) | 1982-09-20 | 1982-09-20 | Oxidation preventing paint composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5953555A true JPS5953555A (en) | 1984-03-28 |
JPS6116778B2 JPS6116778B2 (en) | 1986-05-02 |
Family
ID=15777559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16362982A Granted JPS5953555A (en) | 1982-09-20 | 1982-09-20 | Oxidation preventing paint composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5953555A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62195271U (en) * | 1986-05-30 | 1987-12-11 | ||
JPH0193676U (en) * | 1987-12-15 | 1989-06-20 |
-
1982
- 1982-09-20 JP JP16362982A patent/JPS5953555A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6116778B2 (en) | 1986-05-02 |
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