JPS63270773A - Heat-resistant anticorrosive coating composition - Google Patents

Heat-resistant anticorrosive coating composition

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Publication number
JPS63270773A
JPS63270773A JP62107213A JP10721387A JPS63270773A JP S63270773 A JPS63270773 A JP S63270773A JP 62107213 A JP62107213 A JP 62107213A JP 10721387 A JP10721387 A JP 10721387A JP S63270773 A JPS63270773 A JP S63270773A
Authority
JP
Japan
Prior art keywords
heat
filler
weight
parts
inorganic filler
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
JP62107213A
Other languages
Japanese (ja)
Other versions
JP2561837B2 (en
Inventor
Hiroshi Hashimoto
洋 橋本
Kazuhiro Tomita
和博 冨田
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.)
SWCC Corp
Original Assignee
Showa Electric Wire and Cable Co
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 Showa Electric Wire and Cable Co filed Critical Showa Electric Wire and Cable Co
Priority to JP62107213A priority Critical patent/JP2561837B2/en
Publication of JPS63270773A publication Critical patent/JPS63270773A/en
Application granted granted Critical
Publication of JP2561837B2 publication Critical patent/JP2561837B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain an anticorrosive coating compsn. capable of readily forming a coating film having excellent heat resistance and flexibility and improved chemical resistance, by dissolving or dispersing a polyborosiloxane resin and an inorg. filler in an org. solvent. CONSTITUTION:An anticorrosive coating compsn. is obtd. by dissolving or dispersing a polyborosiloxane resin (a) and an inorg. filler (b) in an org. solvent. Remarkable chemical resistance improvement can be attained by employing an inorg. filler meeting either of the following conditions (i) and (ii). (i): at least a conductive filler, such as a metallic filler, and an anticorrosive filler, such as a ceramic filler, are used. (ii): at least two types of inorg. fillers, of the same kind or different kinds, having different average particle sizes d1 and d2 are employed, said d1 and d2 satisfying the relationship d1<=15mu and d1/d2>=5, with the proviso that d1>=d2.

Description

【発明の詳細な説明】 [発明の目的] (産業上の利用分野) 本発明は、耐薬品性を改善したポリボロシロキサ21勺
脂を用いた耐熱性)93食塗料に関する。
DETAILED DESCRIPTION OF THE INVENTION [Object of the Invention] (Industrial Field of Application) The present invention relates to a heat-resistant) 93 food paint using polyborosiloxa 21 fat with improved chemical resistance.

(従来の技術) 従来より、耐熱性防食塗料として、シリコーン樹脂を主
成分とする塗料が知られており、この塗料を用いて形成
した塗膜は、抗水性に匿れ、また耐薬品性にも優れてい
るという長所を有する反面、耐熱温度がせいぜい250
°C程度であるため、使用I11途が限定されている。
(Prior art) Paints whose main component is silicone resin have been known as heat-resistant anti-corrosion paints, and the coatings formed using these paints have water resistance and chemical resistance. Although it has the advantage of being excellent, the heat resistance temperature is only 250℃ at most.
Since the temperature is around 11°C, its uses are limited.

一方、近年、ポリボロシロキサン樹脂を主成分として有
機溶剤に溶解した塗料を基体に塗布し、これを高温で焼
成することにより、無機化、すなわちセラミックス化さ
せて得られる塗膜が、/100°C以上の温度の常用に
耐えうる等、優れた耐熱性を有していることから注目さ
れている。
On the other hand, in recent years, a paint film containing polyborosiloxane resin as the main component dissolved in an organic solvent is coated on a substrate and fired at high temperatures, resulting in a mineralized, or ceramic, coating film with an angle of /100°. It is attracting attention because it has excellent heat resistance, such as being able to withstand regular use at temperatures of C or higher.

(発明が解決しようとする問題点) しかしながら、このポリボロシロキサン樹脂を用いた塗
料により得られる塗膜は、上述したように耐熱性にすぐ
れるという長所を有する反面、耐薬品性(耐酸、耐アル
カリ)が悪いという問題があり、これにより使用用途が
限定されてしまい、さらに広い用途に使用可能な耐熱性
塗料が強く望まれている。
(Problems to be Solved by the Invention) However, while the coating film obtained with the paint using this polyborosiloxane resin has the advantage of excellent heat resistance as described above, it has poor chemical resistance (acid resistance, resistance to However, there is a problem that paints are not resistant to alkali (alkali), which limits their usage, and there is a strong desire for heat-resistant paints that can be used in a wider range of applications.

本発明はこのような従来の問題点を解決するためになさ
れたもので、耐熱性および可撓性に優れた塗膜を容易に
形成することができ、かつ得られる塗膜の耐薬品性を向
上させた耐熱性防食塗料を提供することを目的とする。
The present invention was made to solve these conventional problems, and it is possible to easily form a coating film with excellent heat resistance and flexibility, and to improve the chemical resistance of the resulting coating film. The purpose of the present invention is to provide an improved heat-resistant anticorrosive paint.

[発明の構成] (問題点を解決するための手段) 本発明の耐熱性防食塗料は、(イ)ポリボロシロキサン
樹脂と、(ロ)無機質充填剤とを有機溶剤に溶解または
分散してなること、および(イ)ポリボロシロキサン樹
脂と、(イ′)シリコーン樹脂と、(ロ)、g機質充填
剤とを有機溶剤に溶解または分散してなることを特徴と
している。
[Structure of the Invention] (Means for Solving the Problems) The heat-resistant anticorrosive paint of the present invention is obtained by dissolving or dispersing (a) a polyborosiloxane resin and (b) an inorganic filler in an organic solvent. It is characterized in that (a) a polyborosiloxane resin, (a) a silicone resin, and (b) a structural filler are dissolved or dispersed in an organic solvent.

本発明に使用する(イ)のポリボロシロキサン(A脂は
、公知のものを使用することができ、下記<I)式でそ
の主骨格が示されるものである。
As the polyborosiloxane (A) used in the present invention, any known polyborosiloxane (A resin) can be used, and its main skeleton is represented by the following formula <I).

(以下余白) また、本発明においてはこのポリボロシロキサン樹脂と
併用して(イ′)のシリコーン樹脂を使用することが可
能である。
(The following is a blank space) In the present invention, it is also possible to use the silicone resin (a') in combination with this polyborosiloxane resin.

このシリコーン樹脂を使用する場合の配合量は、(イ)
のポリボロシロキサン樹脂100重量部に対して、5〜
500重量部の範囲が好ましい、シリコーン樹脂の配合
量が5重量部未満であると塗膜の可撓性向上の効果が十
分に得られず、500重量部を超えるとポリボロシロキ
サン樹脂の優れた耐熱性が減殺される。   。
When using this silicone resin, the blending amount is (a)
5 to 100 parts by weight of polyborosiloxane resin
A range of 500 parts by weight is preferable. If the amount of silicone resin is less than 5 parts by weight, the effect of improving the flexibility of the coating film will not be sufficiently obtained, and if it exceeds 500 parts by weight, the excellent properties of the polyborosiloxane resin will not be obtained. Heat resistance is reduced. .

また、本発明に使用される(口)の無機質充填剤として
は、アルミニウム、銅、銅合金、鉄、ステンレス鋼等の
金属、酸化マグネシウム、醇化アルミニウム、酸化銅、
酸化鉄、酸化ジルコニウム、酸化チタン、酸化クロム、
酸化コバルト、酸化ニッケル、酸化マンガン、酸化モリ
ブデン、酸化タングステン、酸化ランタン、酸化アンチ
モン、酸化ビスマス、酸化バナジウム、雲母等の金属酸
化物、酸1ヒジルコニウム、酸化マグネシウム、酸化チ
タン、酸1ヒホウ素、酸化アルミニウム、酸化トリウム
、酸化ウラン、酸化ケイ素、ケイ酸ジルコニウム等の酸
化物系セラミックス、炭化ケイ素、炭化チタン、炭化ジ
ルコニウム、ポウ化チタン、ホウ化ジルコニウム、窒化
チタン、窒化ポウ索、窒1ヒアルミニウム、窒化ケイ素
、ケイ化モリブデン等の非酸1ヒ物系セラミツクス、S
カラス、Cガラス、Sカラス、Aガラス、Dガラス、チ
タン酸カリウム等があげられ、これらは単独で使用して
もよく、また混合して使用してもよいが、少なくとも下
記のいずれかに該当するようにiH択することにより、
耐薬品性が格段に向上する。
In addition, the inorganic fillers used in the present invention include metals such as aluminum, copper, copper alloys, iron, stainless steel, magnesium oxide, aluminum oxide, copper oxide,
iron oxide, zirconium oxide, titanium oxide, chromium oxide,
Metal oxides such as cobalt oxide, nickel oxide, manganese oxide, molybdenum oxide, tungsten oxide, lanthanum oxide, antimony oxide, bismuth oxide, vanadium oxide, mica, monohydirconium acid, magnesium oxide, titanium oxide, monoarsenic boron acid, Oxide ceramics such as aluminum oxide, thorium oxide, uranium oxide, silicon oxide, zirconium silicate, silicon carbide, titanium carbide, zirconium carbide, titanium boride, zirconium boride, titanium nitride, porous nitride, hyaluminum nitride , non-acid monoarsenic ceramics such as silicon nitride and molybdenum silicide, S
Glass, C glass, S glass, A glass, D glass, potassium titanate, etc. may be used alone or in combination, but at least one of the following applies. By selecting iH to
Chemical resistance is greatly improved.

■ 金属系のような導電性充填剤とセラミックス系のよ
うな防食性充填剤の少なくとも2種を使用する。
■ Use at least two types of fillers: a conductive filler such as a metal type filler and an anticorrosive filler such as a ceramic type filler.

■ 同fif!または異種の平均粒径の異なる2種以上
の無機質充填剤を使用し、かつこれらの無機質充填剤の
各々の平均粒径d1およびd2が、dl>d2の場合、 dl ≦15μ印 かつd + /’ l−12≧5 を満足させる。
■ Same fif! Or, if two or more types of inorganic fillers with different average particle sizes are used, and the average particle sizes d1 and d2 of each of these inorganic fillers are dl>d2, dl ≦15μ mark and d + / ' Satisfy l-12≧5.

また、有機溶剤に溶解または分散後の無機質充填剤の平
均粒径(lと平均厚さtが下記の条件を満足するように
撹拌榮件を設定しても同等の効果か得られる。
Furthermore, the same effect can be obtained by setting the stirring conditions so that the average particle diameter (l) and average thickness t of the inorganic filler after being dissolved or dispersed in an organic solvent satisfy the following conditions.

d≦ 7μm かつd/t≧3 この(ロ)の無機質充填剤の配合量は、(イ)のポリボ
ロシロキサン樹脂100重量部に対して、あるいはこの
(イ)成分と(イ′)のシリコーン樹脂との合計量10
0重藁重員対して、5〜500重量部の範囲が好ましい
。無機質充填剤の配合量が5重量部未満であると耐熱軟
化特性向上効果が十分に得られず、500重量部を超え
ると塗膜の機械的特性が乏しくなる。
d≦7μm and d/t≧3 The blending amount of the inorganic filler (B) is based on 100 parts by weight of the polyborosiloxane resin (A), or this component (A) and the silicone (A′) are mixed. Total amount with resin 10
The amount is preferably in the range of 5 to 500 parts by weight based on 0 weight of straw. If the amount of the inorganic filler is less than 5 parts by weight, the effect of improving heat resistance and softening properties will not be sufficiently obtained, and if it exceeds 500 parts by weight, the mechanical properties of the coating film will be poor.

なお、本発明においては、本発明の効果を損なわない範
囲で、上述の各成分の他に公知の着色顔料、焼付硬化触
媒、その他の添加剤を添加することができる。
In addition, in the present invention, known coloring pigments, baking curing catalysts, and other additives may be added in addition to the above-mentioned components within a range that does not impair the effects of the present invention.

本発明の耐熱性防食塗料は、例えば次のようにして製造
される。
The heat-resistant anticorrosive paint of the present invention is manufactured, for example, as follows.

すなわら、(イ)、(ロ)の各成分を所定の比率で、N
−メチル−2−ピロリドン、ジメチルホルムアミド等の
極性有lR溶剤やトルエン、キシレン等の非極性有機溶
剤に溶解または分散させるか、あるいは予め同様な有R
溶剤に溶解または分散させて液状にしたものを混合し、
これを十分に撹拌することにより得られる。
In other words, N
-Dissolved or dispersed in a polar solvent such as methyl-2-pyrrolidone or dimethylformamide, or a non-polar organic solvent such as toluene or xylene, or dissolved or dispersed in a similar solvent in advance.
Mix the liquid by dissolving or dispersing it in a solvent,
It can be obtained by stirring this thoroughly.

このようにして得られた本発明の耐熱性防食塗料は、金
属板等の基体上に通常の方法にて塗布し、焼付けること
により、耐熱性に優れ、さらに耐薬品性も良好な塗膜が
形成される。
The thus obtained heat-resistant anticorrosive paint of the present invention can be coated onto a substrate such as a metal plate by a conventional method and baked to form a coating film with excellent heat resistance and also good chemical resistance. is formed.

(作 用) そして上記の手段を用いることにより、耐熱温度400
°C以上という優れた耐熱性を満足しつつ、耐薬品性に
も優れた塗膜が得られる。
(Function) By using the above-mentioned means, heat resistant temperature 400
It is possible to obtain a coating film that satisfies excellent heat resistance of at least °C and also has excellent chemical resistance.

(実施例) 次に、本発明の実施例について説明する。(Example) Next, examples of the present invention will be described.

実施例1 ボリボ17シロキサン樹脂100重量部をN−メチル−
2−ピロリドン80重量部に溶解させて樹脂溶液Aを得
た。
Example 1 100 parts by weight of Volivo 17 siloxane resin was mixed with N-methyl-
Resin solution A was obtained by dissolving it in 80 parts by weight of 2-pyrrolidone.

次に、この樹脂溶液A100重量部に対して、導電性充
填剤としてグラファイトフレーク20重員部と防食性充
填剤としてカラスフレーク20重量部とを添加して、ミ
キサーで3時間撹拌して耐熱性防食塗料を得た。
Next, 20 parts by weight of graphite flakes as a conductive filler and 20 parts by weight of crow flakes as an anticorrosive filler were added to 100 parts by weight of this resin solution A, and the mixture was stirred with a mixer for 3 hours to obtain heat-resistant An anticorrosion paint was obtained.

このようにして得た耐熱性防食塗料を用いて、アルミメ
ッキ鋼板にスプレーガンにより塗布し、400℃のiH
度で30分間加熱焼成して塗膜を形成し7た。次いで、
得られた塗膜の400°C耐熱性、耐酸性および耐アル
カリ性の各試験を行った。その結果を第1表に示す。
Using the heat-resistant anticorrosive paint obtained in this way, it was applied to an aluminized steel plate using a spray gun and heated to an iH temperature of 400°C.
A coating film was formed by heating and baking at 30°C for 30 minutes. Then,
The resulting coating film was tested for heat resistance at 400°C, acid resistance, and alkali resistance. The results are shown in Table 1.

実施例2 実施例1で得た樹脂溶液Aに、実施例1と同量のグラフ
ァイトフレークとガラスフレークとを添加し、アトライ
タで20時間撹拌して耐熱性防食塗下゛1を作製し、こ
の1rJf熱性1!/j食塗v1を用いて実施例1と同
様の試験を行った。その結果を第1表に示す。
Example 2 The same amount of graphite flakes and glass flakes as in Example 1 were added to the resin solution A obtained in Example 1, and the mixture was stirred with an attritor for 20 hours to prepare heat-resistant anticorrosive coating 1. 1rJf fever 1! The same test as in Example 1 was conducted using /j food coating v1. The results are shown in Table 1.

なお、表中の比較例は、樹脂溶液Aのみを用いて実施例
1と同一条件で塗膜を形成したちのく比較例1)と、樹
脂溶液A100重量部にカラスフレーク20重量部を添
加して実施例1と同一条件で塗、膜を形成したもの(比
較例1)の試験結果である。
The comparative examples in the table include Chinoku Comparative Example 1) in which a coating film was formed using only resin solution A under the same conditions as Example 1, and 20 parts by weight of crow flakes added to 100 parts by weight of resin solution A. These are the test results of a film formed by coating under the same conditions as in Example 1 (Comparative Example 1).

これらの結果も合せて第1表に示す。These results are also shown in Table 1.

(以下余白) 第  1  表 *1:  400℃で保持し、塗膜にクラックまたは剥
離の発生した時間で示す(以下同じ)。
(The following is a margin.) Table 1 *1: It is held at 400°C and is shown by the time at which cracks or peeling occurred in the coating film (the same applies below).

*2:80℃の10%1I2so、溶液に浸漬し、基材
の腐食が発生した時間で示す(以下同じ)。
*2: Indicates the time taken for corrosion of the base material to occur after being immersed in a 10% 1I2so solution at 80°C (the same applies below).

*3:80℃の10%NaOH溶液に浸漬し、基材の腐
食が発生した時間で示す(以下同じ)。
*3: Indicates the time taken for corrosion of the base material to occur after immersion in a 10% NaOH solution at 80°C (the same applies below).

実施例3.11 ポリボロシロキサン樹脂100重量部とシリコーン樹脂
100重1部とをN−メチル−2−ピロリドン80重蚤
部に溶解させてβ(脂溶液Bを得た。
Example 3.11 100 parts by weight of polyborosiloxane resin and 1 part by weight of 100 parts by weight of silicone resin were dissolved in 80 parts by weight of N-methyl-2-pyrrolidone to obtain β(fat solution B).

次に、この樹脂溶液Bに実施例1と同量のグラフアイl
−フレークとガラスフレークとを添加して、実施例1と
同様にミキサーで3時間撹拌した耐熱性防食塗料(実施
例3)と実施例2と同様にアトライタで20時間撹拌し
たIvJ熱性防食塗料(実施例4)をそれぞれ得た。
Next, the same amount of graphite l as in Example 1 was added to this resin solution B.
- A heat-resistant anticorrosive paint (Example 3) in which flakes and glass flakes were added and stirred for 3 hours in a mixer in the same manner as in Example 1; and an IvJ heat-resistant anticorrosive paint in which flakes and glass flakes were added and stirred in an attritor for 20 hours in the same manner as in Example 2 (Example 3); Example 4) were obtained.

このようにして得た各耐熱性防食塗料を用いて、実施例
1と同一条件で塗膜を形成し、実施例1と同様の試験を
行った。その結果を第2表に示す。
Using each heat-resistant anticorrosive paint thus obtained, a coating film was formed under the same conditions as in Example 1, and the same tests as in Example 1 were conducted. The results are shown in Table 2.

なお、表中の比較例は、樹脂溶液Bのみを用いて実施例
3と同一条件で塗膜を形成したもの(比較例3)と、樹
脂溶液B100重量部にガラスフレーク20.jlij
部を添加して実施例3と同一条件で塗膜を形成したちの
く比較例4)の試験結果である。
Note that the comparative examples in the table include one in which a coating film was formed using only resin solution B under the same conditions as in Example 3 (comparative example 3), and one in which a coating film was formed using only resin solution B under the same conditions as in Example 3 (comparative example 3), and one in which a coating film was formed using 100 parts by weight of resin solution B and 20. jlij
These are the test results of Chinoku Comparative Example 4) in which a coating film was formed under the same conditions as Example 3 with the addition of 50%.

これらの結果も合せて第2表に示す。These results are also shown in Table 2.

第  2  表 実施例5〜7 実施例1で得た樹脂溶液A100重量部に対して、平均
粒径が20μ+m 、12.um、8μIIl、3μ+
n、1μIn、0.8μmll、0.2μ++1ノアル
ミナ扮末をそれぞれ第3表に示す配合@M″添加し、各
々ボールミルで20時間口l拌してそれぞれi5J熱性
防食塗料を得た。
Table 2 Examples 5 to 7 Based on 100 parts by weight of the resin solution A obtained in Example 1, the average particle size was 20 μ+m, 12. um, 8μIIl, 3μ+
n, 1μIn, 0.8μml, and 0.2μ++1 noalumina powder were added in the formulation @M'' shown in Table 3, and mixed in a ball mill for 20 hours to obtain i5J thermal anticorrosive paints.

これらの耐熱性防食塗料を用いて、ステンレス板(SO
8304>に塗布し、400°Cで30分間焼成して塗
膜を形成した0次いで、得られた各塗膜の500℃耐熱
性(基慇目テスト)、耐酸性、耐アルカリ性、耐蒸気性
および折曲げ性の各試験を行った。その結果を第4表に
示す。
Using these heat-resistant anti-corrosion paints, stainless steel plates (SO
8304> and baked at 400°C for 30 minutes to form a coating film.Then, the resulting coating film had 500°C heat resistance (standard test), acid resistance, alkali resistance, and steam resistance. and bendability tests were conducted. The results are shown in Table 4.

また、表中の比較例はアルミナ粉末の種類を変えて添加
し、実施例5と同一条件で耐熱性防食塗v1を作製し、
同様に形成した各塗膜の試験結果である。これらの結果
も合せて第4表に示す。
In addition, in the comparative example in the table, a heat-resistant anticorrosive coating v1 was prepared under the same conditions as Example 5 by adding different types of alumina powder,
These are test results for each coating film formed in the same manner. These results are also shown in Table 4.

(以下余白) 第3表 第4表 、4:  500’Cで保持した後の基pAl11テス
ト(100マスによる粘着デーグチスト後の残存マス数
で示す、ンによる(以下同じ)。
(Margin below) Table 3 Table 4, 4: Group pAl11 test after holding at 500'C (indicated by the number of remaining squares after adhesion testing with 100 squares, according to n (the same applies hereinafter).

*5:  130℃蒸気による塗膜のクランクまたは剥
離発生時間で示す(以下同じ)。
*5: Indicates the time required for the coating film to crack or peel off due to 130°C steam (the same applies below).

に  isooに曲げた際の凸部のクラック発生の有無
で示ずく以下同じ)。
(The same applies below).

実施例8〜10 実施例1で得た樹脂塗料A 100gB、1部に対して
、ガラスフレーク(平均粒径10μm、平均J7さ4μ
m)を添加し、下記の各条件で撹拌して各々耐熱性防食
塗料を得た。
Examples 8 to 10 Glass flakes (average particle size 10 μm, average J7 size 4 μm
m) was added and stirred under the following conditions to obtain heat-resistant anticorrosive paints.

実施例8 ニアトライタで10時間撹拌。Example 8 Stirring with a near triter for 10 hours.

実施例9 ニアトライタで20時間li1拌。Example 9 Li1 stirring for 20 hours with a near writer.

実施例10:ボールミルで30時間137.拌。Example 10: Ball mill for 30 hours 137. Stir.

このようにして得た各耐熱性防食塗料中に分散されてい
るガラスフレークの平均粒径および平均J7さを測定し
た。その結果を第5表に示す。
The average particle diameter and average J7 diameter of the glass flakes dispersed in each of the heat-resistant anticorrosive paints thus obtained were measured. The results are shown in Table 5.

次に、これらの各耐熱性防食塗料を用いて、ステンレス
板(SUS 430 >にスプレーガンによりgjミ布
し、/100℃の温度で30分間加熱焼成して塗膜を形
成した6次いで、得られた各塗1摸の500℃耐熱性(
基盤ロチスト)、耐酸性、耐アルカリ性および折曲げ性
の各試験を行った。その結果を第5表に示す。
Next, each of these heat-resistant anticorrosive paints was applied to a stainless steel plate (SUS 430) using a spray gun, and baked at a temperature of 100°C for 30 minutes to form a coating film. 500℃ heat resistance of each coat (
Tests were conducted on the base rotist, acid resistance, alkali resistance, and bendability. The results are shown in Table 5.

なお、宍中の各比較例は、実施例8と同一の混合溶液を
下記の各条件で撹拌して得たa(熱性防食塗料中に分散
されているガラスフレークの平均粒径および平均厚さと
、これらのiVJ熱性防食塗↑1を用いて実施例8と同
一条件で形成した各g!!膜の試験結果である。これら
の結果も合せて第5表に示す。
In addition, each comparative example of Shishichu was obtained by stirring the same mixed solution as in Example 8 under the following conditions. , are the test results of each g!! film formed using these iVJ thermal anticorrosion coating ↑1 under the same conditions as in Example 8. These results are also shown in Table 5.

比較例9 :盲速ミキサで3時間撹拌。Comparative Example 9: Stirred for 3 hours with a blind speed mixer.

比較例10ニアトライタで5時間fi2拌。Comparative Example 10 Fi2 stirring for 5 hours with a near writer.

比較例11ニアトライタで40時間撹拌。Comparative Example 11 Stirred for 40 hours with a near writer.

比較例12:ボールミルで20時間撹拌。Comparative Example 12: Stirred in a ball mill for 20 hours.

(以下金白) 第5表 [発明の効果コ 以上の実施例からも明らかなように本発明の耐熱性防食
塗料は、優れた耐熱性を有しているのみならず、塗膜の
耐薬品性も優れており、各種用途に広く適用することが
できる。
(Hereinafter referred to as "Kinpaku") Table 5 [Effects of the Invention] As is clear from the above examples, the heat-resistant anticorrosive paint of the present invention not only has excellent heat resistance but also has chemical resistance of the coating film. It has excellent properties and can be widely applied to various uses.

出願人      昭和電線電纜株式会社代理人 弁理
士  須 山 佐 − (ばか1名) 手続ネrti正書 昭和62年8 月28  日 Vf訂庁長官 小川 邦人・殿 昭和62年特許願第107213号 2 発明の名称 耐熱性防食塗料 3 補正をする者 事件との関係   特許出願人 川崎市川崎区小田栄2丁目1番1号 (225)昭和雷FA電島株式会社 代表者   土 1) 芳 男 4  代  理  人 東京都千代田区神田多町2丁目1番地 (ばか1名) 5 補正命令の日付 6 補正の対象 明細出のツて明の詳細な説明の欄。
Applicant Showa Cable and Wire Co., Ltd. Agent Patent Attorney Sa Suyama - (1 idiot) Procedural Nerti Official Book August 28, 1988 Vf Correction Agency Director Kunito Ogawa 1988 Patent Application No. 107213 2 Invention Name of heat-resistant anti-corrosion paint 3 Relationship with the case of the person making the amendment Patent applicant 2-1-1 Oda Sakae, Kawasaki-ku, Kawasaki City (225) Showa Rai FA Denjima Co., Ltd. Representative Sat 1) Yoshio 4 Representative Person: 2-1 Kanda Tamachi, Chiyoda-ku, Tokyo (1 idiot) 5 Date of amendment order 6 Column for detailed explanation of the details of the statement subject to amendment.

7 補正の内容 (1)明IfII1gi第9頁第6〜7行の「ジメチル
ホルムアミド」を[ジメチルアセミーアミド」と訂正す
る。
7 Contents of the amendment (1) "Dimethylformamide" on page 9, lines 6-7 of MeiIfII1gi is corrected to "dimethylacemamide."

(2)明a出第13頁第3行の「80」を1160」と
訂正する。
(2) Correct ``80'' in line 3 of page 13 of Appearance A to ``1160.''

以  上that's all

Claims (10)

【特許請求の範囲】[Claims] (1)(イ)ポリボロシロキサン樹脂と、 (ロ)無機質充填剤とを有機溶剤に溶解または分散して
なることを特徴とする耐熱性防食塗料。
(1) A heat-resistant anticorrosive paint characterized by dissolving or dispersing (a) a polyborosiloxane resin and (b) an inorganic filler in an organic solvent.
(2)(ロ)の無機質充填剤として、導電性充填剤と防
食性充填剤の少なくとも2種を含有する特許請求の範囲
第1項記載の耐熱性防食塗料。
(2) The heat-resistant anticorrosive paint according to claim 1, which contains at least two types of conductive fillers and anticorrosion fillers as the inorganic filler (b).
(3)(ロ)の無機質充填剤として、同種または異種の
平均粒径の異なる2種以上の無機質充填剤を含有し、か
つこれらの無機質充填剤の各々の平均粒径d_1および
d_2が、d_1>d_2の場合、d_1≦15μm かつd_1/d_2≧5 を満足する特許請求の範囲第1項記載の耐熱性防食塗料
(3) The inorganic filler in (b) contains two or more types of inorganic fillers of the same type or different types with different average particle sizes, and the average particle sizes d_1 and d_2 of each of these inorganic fillers are d_1 >d_2, the heat-resistant anticorrosive paint according to claim 1, which satisfies d_1≦15 μm and d_1/d_2≧5.
(4)有機溶剤に溶解または分散後の(ロ)の無機質充
填剤の平均粒径dと平均厚さtが、 d≦7μm かつd/t≧3 を満足する特許請求の範囲第1項記載の耐熱性防食塗料
(4) Claim 1, wherein the average particle diameter d and average thickness t of the inorganic filler (b) after being dissolved or dispersed in an organic solvent satisfy d≦7 μm and d/t≧3. Heat-resistant anti-corrosion paint.
(5)(イ)のポリボロシロキサン樹脂100重量部あ
たり、 (ロ)の無機質充填材5〜500重量部含有する特許請
求の範囲第1項ないし第4項のいずれか1項記載の耐熱
性防食塗料。
(5) The heat resistance according to any one of claims 1 to 4, which contains 5 to 500 parts by weight of the inorganic filler (b) per 100 parts by weight of the polyborosiloxane resin (a). Anti-corrosion paint.
(6)(イ)ポリボロシロキサン樹脂と、 (イ′)シリコーン樹脂と、 (ロ)無機質充填剤とを有機溶剤に溶解または分散して
なることを特徴とする耐熱性防食塗料。
(6) A heat-resistant anticorrosive paint characterized by dissolving or dispersing (a) a polyborosiloxane resin, (a') a silicone resin, and (b) an inorganic filler in an organic solvent.
(7)(ロ)の無機質充填剤として、導電性充填剤と防
食性充填剤の少なくとも2種を含有する特許請求の範囲
第6項記載の耐熱性防食塗料。
(7) The heat-resistant anticorrosive paint according to claim 6, which contains at least two types of conductive filler and anticorrosive filler as the inorganic filler (b).
(8)(ロ)の無機質充填剤として、同種または異種の
平均粒径の異なる2種以上の無機質充填剤を含有し、か
つこれらの無機質充填剤の各々の平均粒径d_1および
d_2が、d_1>d_2の場合、d_1≦15μm かつd_1/d_2≧5 を満足する特許請求の範囲第6項記載の耐熱性防食塗料
(8) The inorganic filler in (b) contains two or more types of inorganic fillers of the same type or different types with different average particle sizes, and the average particle sizes d_1 and d_2 of each of these inorganic fillers are d_1 >d_2, the heat-resistant anticorrosive paint according to claim 6, which satisfies d_1≦15 μm and d_1/d_2≧5.
(9)有機溶剤に溶解または分散後の(ロ)の無機質充
填剤の平均粒径dと平均厚さtが、 d≦7μm かつd/t≧3 を満足する特許請求の範囲第6項記載の耐熱性防食塗料
(9) Claim 6, wherein the average particle diameter d and average thickness t of the inorganic filler (b) after being dissolved or dispersed in an organic solvent satisfy d≦7 μm and d/t≧3. Heat-resistant anti-corrosion paint.
(10)(イ)のポリボロシロキサン樹脂100重量部
あたり、 (イ′)のシリコーン樹脂5〜500重量部含有し、か
つ(イ)のポリボロシロキサン樹脂と(イ′)のシリコ
ーン樹脂との合計量100重量部あたり、 (ロ)の無機質充填材5〜500重量部含有する特許請
求の範囲第6項ないし第9項のいずれか1項記載の耐熱
性防食塗料。
(10) Contains 5 to 500 parts by weight of the silicone resin (A') per 100 parts by weight of the polyborosiloxane resin (A), and contains a combination of the polyborosiloxane resin (A) and the silicone resin (A'). The heat-resistant anticorrosive paint according to any one of claims 6 to 9, which contains 5 to 500 parts by weight of the inorganic filler (b) per 100 parts by weight in total.
JP62107213A 1987-04-30 1987-04-30 Heat and chemical resistant paint Expired - Lifetime JP2561837B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62107213A JP2561837B2 (en) 1987-04-30 1987-04-30 Heat and chemical resistant paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62107213A JP2561837B2 (en) 1987-04-30 1987-04-30 Heat and chemical resistant paint

Publications (2)

Publication Number Publication Date
JPS63270773A true JPS63270773A (en) 1988-11-08
JP2561837B2 JP2561837B2 (en) 1996-12-11

Family

ID=14453354

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62107213A Expired - Lifetime JP2561837B2 (en) 1987-04-30 1987-04-30 Heat and chemical resistant paint

Country Status (1)

Country Link
JP (1) JP2561837B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007284468A (en) * 2006-04-12 2007-11-01 Hitachi Chem Co Ltd Resin composition and film-forming material comprising the same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57200462A (en) * 1981-06-02 1982-12-08 Showa Electric Wire & Cable Co Ltd Heat-resistant coating
JPS59100169A (en) * 1982-12-01 1984-06-09 Showa Electric Wire & Cable Co Ltd Heat-resistant paint and heat-resistant insulated wire
JPS59218844A (en) * 1983-05-27 1984-12-10 松下電器産業株式会社 Infrared radiation coating
JPS6088082A (en) * 1983-10-20 1985-05-17 Matsushita Electric Ind Co Ltd Infrared ray radiating film
JPS60213743A (en) * 1984-04-09 1985-10-26 Matsushita Electric Ind Co Ltd Infrared ray radiator
JPS60231769A (en) * 1984-04-30 1985-11-18 Showa Electric Wire & Cable Co Ltd Heat-resistant paint

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57200462A (en) * 1981-06-02 1982-12-08 Showa Electric Wire & Cable Co Ltd Heat-resistant coating
JPS59100169A (en) * 1982-12-01 1984-06-09 Showa Electric Wire & Cable Co Ltd Heat-resistant paint and heat-resistant insulated wire
JPS59218844A (en) * 1983-05-27 1984-12-10 松下電器産業株式会社 Infrared radiation coating
JPS6088082A (en) * 1983-10-20 1985-05-17 Matsushita Electric Ind Co Ltd Infrared ray radiating film
JPS60213743A (en) * 1984-04-09 1985-10-26 Matsushita Electric Ind Co Ltd Infrared ray radiator
JPS60231769A (en) * 1984-04-30 1985-11-18 Showa Electric Wire & Cable Co Ltd Heat-resistant paint

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007284468A (en) * 2006-04-12 2007-11-01 Hitachi Chem Co Ltd Resin composition and film-forming material comprising the same

Also Published As

Publication number Publication date
JP2561837B2 (en) 1996-12-11

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