JPH01224136A - Slurry mold wash and sliding material - Google Patents

Slurry mold wash and sliding material

Info

Publication number
JPH01224136A
JPH01224136A JP4789488A JP4789488A JPH01224136A JP H01224136 A JPH01224136 A JP H01224136A JP 4789488 A JP4789488 A JP 4789488A JP 4789488 A JP4789488 A JP 4789488A JP H01224136 A JPH01224136 A JP H01224136A
Authority
JP
Japan
Prior art keywords
graphite
viscosity
specified
sliding material
coating
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
JP4789488A
Other languages
Japanese (ja)
Inventor
Akira Kitahara
北原 彰
Takahiko Ema
江間 高彦
Shojiro Sawada
澤田 庄次郎
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.)
Osaka Kasei Co Ltd
Kansai Coke and Chemicals Co Ltd
Original Assignee
Osaka Kasei Co Ltd
Kansai Coke and Chemicals 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 Osaka Kasei Co Ltd, Kansai Coke and Chemicals Co Ltd filed Critical Osaka Kasei Co Ltd
Priority to JP4789488A priority Critical patent/JPH01224136A/en
Publication of JPH01224136A publication Critical patent/JPH01224136A/en
Pending legal-status Critical Current

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  • Mold Materials And Core Materials (AREA)

Abstract

PURPOSE:To prevent the sedimentation/cohesion of a graphite at reserving time by contg. the specified wt.% of a graphite of less than specified grain diameter, the specified % of an interface active agent and the specified % of a cellulose ether and making them at specified viscosity (value at 25 deg.C). CONSTITUTION:The viscosity is adjusted to 500-15,000cps (value at 25 deg.C) as well as containing 20-40wt.% graphite of <=30mum grain diameter, 0.15-3% surface active agent and 0.1-3% cellulose ether. A flaky graphite and earthy graphite are excellent in heat resistance and corrosion resistance and heat resistance and corrosion resistance and used as a coating form and sliding materials by crushing in a proper grain size and making in a slurry by dispersing in a water. The surface active agent is necessary for dispersing a hydrophobic graphite in a water and especially nonionic surface active agent is preferable. The sedimentation/cohesion of a graphite is prevented by adjusting the viscosity of the coating form and sliding material to an optimum value by adding the cellulose ether in a proper amt. The spreading and adhesion onto a coating face are thus good without causing any sedimentation/cohesion at graphite reserving time and the coating face excellent in slidability can be formed.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は黒鉛を基材とする塗型材および摺動材において
保存時黒鉛が沈降・凝集することのないスラリー状の塗
型材および摺動材に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention provides coating materials and sliding materials based on graphite that are in the form of a slurry in which graphite does not settle or aggregate during storage. It is related to.

[従来の技術] 鱗状黒鉛、土状黒鉛等の黒鉛は耐熱性や耐食性に優れて
いるので、適当な粒度に粉砕して水に分散させてスラリ
ー状にして塗型材および摺動材として使用されている。
[Prior art] Graphite such as scaly graphite and earthy graphite has excellent heat resistance and corrosion resistance, so it is crushed to an appropriate particle size and dispersed in water to form a slurry, which is used as a coating material and sliding material. ing.

塗型材および摺動材にはさらに5i02 、AI、O,
、MoS、、BN等の無機物やポリテトラフルオロエチ
レン、オキシベンゾイルポリエステル、弗素樹脂、熱可
塑性芳香族ポリエーテル、芳香族ポリエーテルケトン樹
脂、フルオロカーボン重合体等の有機化合物が粘結材あ
るいはその他添加材として混合されている。
Furthermore, 5i02, AI, O,
, MoS, , BN, and other inorganic substances, and organic compounds such as polytetrafluoroethylene, oxybenzoyl polyester, fluororesins, thermoplastic aromatic polyethers, aromatic polyether ketone resins, and fluorocarbon polymers are used as binders or other additives. It is mixed as.

黒鉛は疎水性であるため界面活性剤で処理して親木性を
与えた粉末状形態としであるいは界面活性剤を用いて水
に分散させ黒鉛濃度30%程度のスラリー状にしたもの
として夫々市販されているが、前者の場合は保存中に黒
鉛が凝集して塊状になり易く、また後者の場合は黒鉛が
沈降して凝集し易く、いずれの場合も塗型材および摺動
材とbて鋳型および耐火煉瓦に塗布する際の撹拌不良。
Since graphite is hydrophobic, it is commercially available in the form of a powder that has been treated with a surfactant to give it wood-philic properties, or as a slurry with a graphite concentration of approximately 30% that has been dispersed in water using a surfactant. However, in the former case, the graphite tends to aggregate and form lumps during storage, and in the latter case, the graphite tends to settle and aggregate, and in both cases, the mold is mixed with the coating material and the sliding material. and poor agitation when applying to refractory bricks.

展着不良、付着不良等の問題、さらには塗膜欠陥や塗面
の摺動性不良等を招く原因となっていた。
This causes problems such as poor spreading and poor adhesion, as well as defects in the coating film and poor sliding properties of the coated surface.

[発明が解決しようとする課題] 本発明者等はこのような状況を憂慮して検討を行い粉末
状として保存する場合の欠陥については別途解決手段を
見付けて特許出願した。そして本発明においてはスラリ
ー状として提供する場合について保存時に黒鉛が下層に
沈降・凝集することがなく、その結果として上記問題を
生ずることのない様な塗型材および摺動材について検討
した。
[Problems to be Solved by the Invention] Concerned about this situation, the inventors of the present invention conducted studies and found a separate solution to the defects in storing the product in powder form, and filed a patent application. In the present invention, we studied coating materials and sliding materials that do not cause the above-mentioned problems because graphite does not settle or aggregate in the lower layer during storage when provided in the form of a slurry.

[課題を解決する為の手段] 上記課題を解決することのできた本発明のスラリー状塗
型材および摺動材は黒鉛を基材とするものであり、 (A)粒径30μm以下の黒鉛:20〜40%(B)界
面活性剤: 0.15〜3% (C)セルロースエーテル:0.1〜3%を含有すると
共に粘度500〜xsooocpsであることを構成要
旨とするものである。
[Means for Solving the Problems] The slurry coating material and sliding material of the present invention that can solve the above problems are based on graphite, and include (A) graphite with a particle size of 30 μm or less: 20 -40% (B) surfactant: 0.15-3% (C) cellulose ether: 0.1-3%, and has a viscosity of 500-xsooocps.

[作用] 本発明の塗型材および摺動材における基材としては鱗片
状黒鉛や玉状黒鉛を天然あるいは合成の如何を問わず使
用することができる。この際黒鉛の粒径は30μm以下
でなければならず、30μmを超えると凝集に基く粒成
長の影響が顕著に現われ、沈降が生じやすくなる0次に
塗型材および摺動材中の黒鉛含有量は20〜40%とす
る。
[Function] As the base material in the coating material and sliding material of the present invention, flaky graphite or globular graphite, whether natural or synthetic, can be used. In this case, the particle size of graphite must be 30 μm or less; if it exceeds 30 μm, the influence of particle growth due to aggregation will become noticeable, and sedimentation will easily occur. is 20 to 40%.

20%未満では黒鉛濃度が低すぎて塗型材および摺動材
としての機能が不十分であり、また粘性不十分となって
塗装垂れを生じ塗膜むらを招き易い、一方40%を超え
ると黒鉛濃度が高すぎて黒鉛同士の凝集・沈降が生じや
すくなり、また塗装作業性が悪くなる。
If the graphite concentration is less than 20%, the graphite concentration will be too low and its function as a coating material and sliding material will be insufficient, and the viscosity will be insufficient, resulting in paint dripping and uneven coating.On the other hand, if it exceeds 40%, the graphite concentration will be insufficient. If the concentration is too high, agglomeration and sedimentation of graphite tend to occur, and painting workability becomes worse.

界面活性剤は疎水性の黒鉛を水に分散させるためには必
要な成分であり、カチオン系、アニオン系、ノニオン系
1両性いずれのものも顕著な発泡を生じない限ぎり自由
に使用できる。もっとも黒鉛のような疎水性物質を水に
分散させるという意味ではノニオン系の界面活性剤を用
いることが望ましく、たとえばノニオン系界面活性剤と
してポリオキシ化合物(ポリオール)の脂肪酸エステル
、ポリエチレンオキサイド縮合物などが挙げられる。そ
して、その添加量は0.15〜3%とする必要があり、
0.15%未満では黒鉛の分散性に難をきたし、3%を
超えて使用しても黒鉛の分散性効果は向上せず、却って
泡立ちを生ずる危険がある。
The surfactant is a necessary component for dispersing hydrophobic graphite in water, and any of cationic, anionic, nonionic, and amphoteric surfactants can be used freely as long as they do not cause significant foaming. However, in the sense of dispersing hydrophobic substances such as graphite in water, it is desirable to use nonionic surfactants. For example, fatty acid esters of polyoxy compounds (polyols), polyethylene oxide condensates, etc. are used as nonionic surfactants. Can be mentioned. And the amount added needs to be 0.15 to 3%,
If it is less than 0.15%, the dispersibility of graphite will be difficult, and if it exceeds 3%, the dispersibility effect of graphite will not be improved, and there is a risk of foaming.

本発明で用いるセルロースエーテルはセルロースのOH
基の一部または全部がエーテル化された化合物であり、
メチルセルロース、エチルセルロース、ヒドロキシエチ
ルセルロース、メチルヒドロキシエチルセルロース、カ
ルボキシメチルセルロース等やこれらの混合物を用いる
ことができる。
The cellulose ether used in the present invention is the OH of cellulose.
A compound in which part or all of the group is etherified,
Methylcellulose, ethylcellulose, hydroxyethylcellulose, methylhydroxyethylcellulose, carboxymethylcellulose, etc., and mixtures thereof can be used.

本発明においてはセルロースエーテルを添加することに
よって塗型材および摺動材の粘度を500〜15000
cpsに調整して黒鉛の沈降・凝集を防止するのである
が、塗型材および摺動材の粘度が500 cps未満で
は黒鉛の沈降・凝集がおこり易く、一方15000cp
sを超えると塗型材および摺動材調整時の撹拌性や塗布
作業性において問題を生ずる。
In the present invention, by adding cellulose ether, the viscosity of the mold coating material and sliding material can be adjusted to 500 to 15,000.
cps is adjusted to prevent sedimentation and agglomeration of graphite, but if the viscosity of the coating material and sliding material is less than 500 cps, sedimentation and aggregation of graphite will easily occur;
If it exceeds s, problems will occur in stirring performance and coating workability when preparing coating material and sliding material.

そして塗型材および摺動材の粘度を上記好適範囲に保つ
ためにはセルロースエーテルの添加量を0.1〜3%、
好ましくは0.2〜1%とする必要がある。
In order to keep the viscosity of the coating material and sliding material within the above-mentioned preferred range, the amount of cellulose ether added should be 0.1 to 3%.
Preferably it needs to be 0.2 to 1%.

さらに本発明の塗型材および摺動材においてはベントナ
イトや粘土、さらに前記した無機物や有機物を本発明の
効果を妨げない範囲で添加することができる。
Furthermore, bentonite, clay, and the above-mentioned inorganic and organic substances can be added to the coating material and sliding material of the present invention within a range that does not impede the effects of the present invention.

[実施例] 実施例1 粒径5〜7μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gと共に水700
gに分散させ、さらにメチルセルロース(1%水溶液の
時の粘度3000cps)10gを加えて粘度5000
 cpsのスラリー状の塗型材および摺動材を得た。
[Example] Example 1 300 g of graphite with a particle size of 5 to 7 μm was mixed with a nonionic surfactant (
700 g of water with 10 g of polyethylene oxide condensate)
g, and further added 10 g of methylcellulose (viscosity of 1% aqueous solution: 3000 cps) to make the viscosity 5000 cps.
A cps slurry coating material and sliding material were obtained.

得られた塗型材および摺動材を10日間放置しても黒鉛
の沈降は見られなかった。ざらに該塗型材および摺動材
を鋳型および耐火煉瓦表面に刷毛塗りしたところ良好な
塗膜が得られ、該塗膜に対しJIS−に−5400に定
められた**試験および加熱試験を行なったところ、く
ぼみ、泡、ふくれ1割れ剥離等を生ずることはなかった
No sedimentation of graphite was observed even after the obtained coating material and sliding material were left for 10 days. When the coating material and sliding material were applied with a brush to the surface of the mold and firebrick, a good coating film was obtained, and the coating film was subjected to the ** test and heating test specified in JIS-5400. As a result, no dents, bubbles, bulges, cracks, or peeling were observed.

実施例2 粒径1〜3μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gと共に水700
gに分散させ、さらにカルボキシメチルセルロース(1
%水溶液の時の粘度300cps ) 10 gを加え
て粘度3000 cpsのスラリー状の塗型材および摺
動材を得た。
Example 2 300 g of graphite with a particle size of 1 to 3 μm was mixed with a nonionic surfactant (
700 g of water with 10 g of polyethylene oxide condensate)
g, and further carboxymethyl cellulose (1
% aqueous solution (viscosity 300 cps) was added to obtain a slurry coating material and sliding material having a viscosity of 3000 cps.

得られた塗型材および摺動材を10日間放置しても黒鉛
の沈降は見られなかった。ざらに該塗型材および摺動材
を鋳型および耐火煉瓦表面にスプレー塗布したところ良
好な塗膜が得られ、該塗膜に対しJIS−に−5400
の衝撃試験および加熱試験を行なったところ、くぼみ、
泡、ふくれ。
No sedimentation of graphite was observed even after the obtained coating material and sliding material were left for 10 days. When the coating material and sliding material were spray applied to the surface of the mold and firebrick, a good coating film was obtained, and the coating film was rated according to JIS-5400.
When we conducted an impact test and a heating test, we found that there were dents,
Bubbles, blisters.

割れ剥離等を生ずることはなかった。No cracking or peeling occurred.

実施例3 粒径5〜7μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gを用いて水70
08に分散させ、さらにメチルヒドロキシエチルセルロ
ース(1%水溶液の時の粘度4000cps)5gを加
えて粘度4000 cpsのスラリー状の塗型材および
摺動材を得た。
Example 3 300 g of graphite with a particle size of 5 to 7 μm was mixed with a nonionic surfactant (
Using 10 g of polyethylene oxide condensate, add 70 g of water.
08 and further added 5 g of methyl hydroxyethyl cellulose (viscosity 4000 cps when 1% aqueous solution) to obtain a slurry coating material and sliding material having a viscosity of 4000 cps.

得られた塗型材および摺動材を10日間放置しても黒鉛
の沈降は見られなかった。ざらに該塗型材および摺動材
を鋳型および耐火煉瓦表面に刷毛塗りしたところ良好な
塗膜が得られ、該塗膜に対しJIS−に−5400のW
1撃試験および加熱試験を行なったところ、くぼみ、泡
、ふくれ5割れ剥離等を生ずることはなかった。
No sedimentation of graphite was observed even after the obtained coating material and sliding material were left for 10 days. When the coating material and sliding material were brushed onto the surface of the mold and firebrick, a good coating film was obtained, and the coating film was rated W of -5400 according to JIS-5.
When a one-shot test and a heating test were conducted, no dents, bubbles, blisters, cracks, or peeling occurred.

実施例4 粒径1〜3μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gと共に水フOO
gに分散させ、さらにヒドロキシエチルセルロース(1
%水溶液の時の粘度250cps)10gを加えて粘度
2000 cpsのスラリー状の塗型材および摺動材を
得た。
Example 4 300 g of graphite with a particle size of 1 to 3 μm was mixed with a nonionic surfactant (
10g of polyethylene oxide condensate) and water OO
g and further dispersed in hydroxyethyl cellulose (1
% aqueous solution (viscosity 250 cps) was added to obtain a slurry coating material and sliding material having a viscosity of 2000 cps.

得られた塗型材および摺動材を10日間放置しても黒鉛
の沈降は見られなかった。ざらに該塗型材および摺動材
を鋳型および耐火煉瓦表面にスプレーで塗布したところ
良好な塗膜が得られ、該塗膜に対しJIS−に−540
0の衝撃試験および加熱試験を行なったところ、くぼみ
、泡、ふくれ1割れ剥離等を生ずることはなかった。
No sedimentation of graphite was observed even after the obtained coating material and sliding material were left for 10 days. When the coating material and sliding material were sprayed onto the surfaces of molds and refractory bricks, a good coating film was obtained, and the coating film was rated according to JIS-540.
When an impact test and a heating test were conducted, no dents, bubbles, blisters, cracks, or peeling occurred.

比較例1 粒径5〜7μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gと共に水700
gに分散させ、粘度100 cpsのスラリー状の塗型
材および摺動材を得た。
Comparative Example 1 300 g of graphite with a particle size of 5 to 7 μm was mixed with a nonionic surfactant (
700 g of water with 10 g of polyethylene oxide condensate)
g to obtain a slurry coating material and sliding material having a viscosity of 100 cps.

得られた塗型材および摺動材を24時間放置すると、黒
鉛は下層に沈降した。
When the obtained coating material and sliding material were left for 24 hours, graphite settled in the lower layer.

比較例2 粒径5〜7μmの黒鉛300gを非イオン界面活性剤(
ポリエチレンオキサイド縮合物)10gと共にを用いて
水700gに分散させ、さらに分子量t 5oooのポ
リビニアルコール10gを加えて粘度20000 cp
sのスラリー状の塗型材および摺動材を得た。
Comparative Example 2 300 g of graphite with a particle size of 5 to 7 μm was mixed with a nonionic surfactant (
10 g of polyethylene oxide condensate) was dispersed in 700 g of water, and 10 g of polyvinyl alcohol with a molecular weight of t 500 was added to give a viscosity of 20,000 cp.
A slurry coating material and sliding material of s were obtained.

得られた塗型材および摺動材を24時間放置すると、黒
鉛は下層に沈降した。
When the obtained coating material and sliding material were left for 24 hours, graphite settled in the lower layer.

比較例3 粒径15〜20μmの黒鉛300gを非イオン界面活性
剤(ポリエチレンオキサイド縮合物)10gを用いて水
フOOgに分散させ、さらに黄色デキストリン10gを
加えて粘度200 cpsのスラリー状の塗型材および
摺動材を得た。
Comparative Example 3 300 g of graphite with a particle size of 15 to 20 μm was dispersed in OOg of water using 10 g of a nonionic surfactant (polyethylene oxide condensate), and 10 g of yellow dextrin was further added to form a slurry-like coating material with a viscosity of 200 cps. and sliding material was obtained.

得られた塗型材および摺動材を24時間放置すると、黒
鉛は下層に沈降した状態となりざらに該塗型材および摺
動材を鋳型および耐火煉瓦表面に刷毛塗りして塗膜を得
、該塗膜に対しJIS−に−5400の**試験を行な
つたところ、くぼみが生じ、ざらにJIS−に−540
0の加熱試験を行なったところ泡1割れが生じた。
When the obtained coating material and sliding material are left for 24 hours, the graphite settles in the lower layer. When the film was subjected to JIS-5400 ** test, dents appeared and it was roughly JIS-540.
When a heating test of 0 was conducted, one bubble broke.

[発明の効果] 本発明は以上のように構成されているので、本発明の塗
型材および摺動材は保存時、黒鉛の沈降・凝集を生ずる
ことがない、このため塗面への展着性や付着性が良好で
あり、さらには塗膜状態もよく摺動性に優れた塗面を形
成する。
[Effects of the Invention] Since the present invention is configured as described above, the coating material and sliding material of the present invention do not cause sedimentation or agglomeration of graphite during storage, and therefore do not spread on the coated surface. It has good properties and adhesion, and also forms a coated surface with good coating properties and excellent sliding properties.

Claims (1)

【特許請求の範囲】 黒鉛を基材とする塗型材および摺動材において、 (A)粒径30μm以下の黒鉛:20〜40%(重量%
の意味、以下同じ) (B)界面活性剤:0.15〜3% (C)セルロースエーテル:0.1〜3% を含有すると共に粘度500〜15000cps(25
℃における値、以下同じ)であることを特徴とするスラ
リー状塗型材および摺動材。
[Claims] In coating materials and sliding materials based on graphite, (A) graphite with a particle size of 30 μm or less: 20 to 40% (wt%);
(the same meaning hereinafter) (B) Surfactant: 0.15 to 3% (C) Cellulose ether: 0.1 to 3% and has a viscosity of 500 to 15,000 cps (25
A slurry-like coating material and sliding material characterized by having a value at °C (the same applies hereinafter).
JP4789488A 1988-03-01 1988-03-01 Slurry mold wash and sliding material Pending JPH01224136A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4789488A JPH01224136A (en) 1988-03-01 1988-03-01 Slurry mold wash and sliding material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4789488A JPH01224136A (en) 1988-03-01 1988-03-01 Slurry mold wash and sliding material

Publications (1)

Publication Number Publication Date
JPH01224136A true JPH01224136A (en) 1989-09-07

Family

ID=12788111

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4789488A Pending JPH01224136A (en) 1988-03-01 1988-03-01 Slurry mold wash and sliding material

Country Status (1)

Country Link
JP (1) JPH01224136A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02165841A (en) * 1988-12-19 1990-06-26 Kao Corp Composition for coating agent for casting
JP2007144511A (en) * 2005-10-31 2007-06-14 Kao Corp Casting structure

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02165841A (en) * 1988-12-19 1990-06-26 Kao Corp Composition for coating agent for casting
JP2007144511A (en) * 2005-10-31 2007-06-14 Kao Corp Casting structure

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