JPH0369384B2 - - Google Patents

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Publication number
JPH0369384B2
JPH0369384B2 JP7271585A JP7271585A JPH0369384B2 JP H0369384 B2 JPH0369384 B2 JP H0369384B2 JP 7271585 A JP7271585 A JP 7271585A JP 7271585 A JP7271585 A JP 7271585A JP H0369384 B2 JPH0369384 B2 JP H0369384B2
Authority
JP
Japan
Prior art keywords
silane
inorganic
binder
ratio
composition
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.)
Expired
Application number
JP7271585A
Other languages
Japanese (ja)
Other versions
JPS61233065A (en
Inventor
Eiji Takeuchi
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.)
TEE ESU BII JUGEN
Original Assignee
TEE ESU BII JUGEN
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 TEE ESU BII JUGEN filed Critical TEE ESU BII JUGEN
Priority to JP7271585A priority Critical patent/JPS61233065A/en
Publication of JPS61233065A publication Critical patent/JPS61233065A/en
Publication of JPH0369384B2 publication Critical patent/JPH0369384B2/ja
Granted legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Silicon Polymers (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、すぐれた長期保存性とコントロール
されたチクソトロピー性をもち作業性のよい無機
系の水性スラリー状組成物で、比較的低温で熱硬
化することにより耐熱性で耐薬品性、耐沸とう水
性などのすぐれたクラツクのない無機系被膜を提
供する無機系組成物用のバインダーに関する。本
発明による無機系組成物はコーテイング剤や充填
剤として利用される。 〔従来の技術〕 従来、部分加水分解したシラン化合物とコロイ
ダルシリカとの反応生成物をバインダーとして、
これにシリカ、アルミナ、ジルコニアなどの無機
粉体を配合した無機系組成物は公知であり、シラ
ン化合物として下記一般式 RSi(OR′)3 (式中、Rは−CH3または
[Industrial Field of Application] The present invention is an inorganic aqueous slurry composition that has excellent long-term storage stability, controlled thixotropy, and good workability. This invention relates to a binder for inorganic compositions that provides crack-free inorganic coatings with excellent chemical resistance and boiling water resistance. The inorganic composition according to the present invention is used as a coating agent or a filler. [Prior Art] Conventionally, a reaction product of a partially hydrolyzed silane compound and colloidal silica is used as a binder.
Inorganic compositions containing inorganic powders such as silica, alumina, and zirconia are well known, and as silane compounds, they have the following general formula RSi(OR') 3 (wherein, R is -CH 3 or

〔発明の目的〕[Purpose of the invention]

本発明の目的は上記の欠点を改良し、これらの
無機系組成物のもつすぐれた耐熱性及びすぐれた
耐薬品性の特長を生かす新規な無機系組成物バイ
ンダーを提供することにある。 〔発明の構成〕 本発明は、前述したシランAまたはBに、一般
式 R″2Si(OR′)2 (式中、R′は−CH3または−C2H5を表し、そし
てR″は−CH3を表す)で示されるシラン化合物、
例えば(CH32Si(OCH32(以下シランCという)
を、ある特定の比率で混合して用いることによ
り、上記の従来品の欠点が解決されることを発見
したことに基づくものである。 ここで、シランCを単独で用いた場合に生じる
欠点としては、 (1) 加熱硬化膜が軟らかくなりすぎる。 (2) 加熱硬化に長時間を要する。 などが挙げられるが、これらの欠点は上記シラン
AまたはBと併用することによつて解決されるこ
とが見い出された。 本発明において、シランAまたはシランBとシ
ランCとの混合比は、重量比で9:1〜1:9の
範囲が好ましく、この範囲を越えると、それぞれ
のシランを単独で用いた場合に生じる欠点が出現
するため好ましくない。 〔実施例〕 以下に本発明を実施例によりさらに詳細に説明
する。 実施例 1 酢酸3gを溶解した純水30gに、シランAとシ
ランCの混合物(下記第1表に示す組成比)100
gを加え、室温にて5〜15分反応させて部分加水
分解シラン化合物をえた。次いで、これにコロイ
ダルシリカ(SiO2として21wt%含有)水溶液250
gを加え、室温で5〜30分間反応させて無機系組
成物バインダーをえた。これに、平均粒径約20μ
mのシリカ粉末400g、約10μmのシリカ粉末100
g及びアルミナ粉末(平均粒径約5μm)100gを
メタノール50gとともに加え、混合物を2〜4日
間静置させて無機系スラリー状組成物No.1〜7を
えた。 スラリーの安定性、塗膜(鉄板上に約2mm厚に
コーテイングし、室温乾燥12時間ののち160℃で
硬化)の硬化速度、耐熱性、外観観察(クラツク
発生の有無、等)などの評価を行つた。結果を第
1表に示す。 実施例 2 実施例1のシランAの代わりにシランBを用
い、実施例1と同様にして無機系スラリー状組成
物No.8〜13をえた。このスラリーの安定性、硬化
性、硬化塗膜特性を評価し、その結果を第2表に
示した。 実施例1及び実施例2から明らかなように、部
分加水分解シランとしてシランA/シランC及び
シランB/シランCの混合物でその重量比が9/
1〜1/9のものを用いることにより諸特性のバ
ランスのとれた無機系組成物バインダー、及びそ
れを利用した無機系スラリー組成物がえられる。 実施例 3 実施例1の無機系スラリー状組成物No.4に用い
たシランA/シランB混合物(1/1重量比)の
加水分解生成物とコロイダルシリカの反応生成物
である無機系バインダー組成物のみ(シリカやア
ルミナなどの粉末を除いた系)を鉄板にコーテイ
ングしたところ透明均一な連続被膜が形成され
た。これを160℃で20分間加熱して硬化させると、
600℃に加熱しても塗膜にワレ、ハクリ、変色を
生ぜず、すぐれた耐熱性の被膜がえられた。 また、この被膜は、沸とう水に1時間浸漬して
もハクリやワレを生ぜず、撥水性を維持してい
た。また、トリクレン、アルコール、ガソリンな
どの有機溶剤に一週間常温で浸漬しても何らの変
化も生ぜず、すぐれた耐熱性、耐沸とう水性、耐
薬品性を有していた。
The object of the present invention is to improve the above-mentioned drawbacks and provide a new inorganic composition binder that takes advantage of the excellent heat resistance and chemical resistance of these inorganic compositions. [Structure of the Invention] The present invention provides that the above-mentioned silane A or B has the general formula R″ 2 Si(OR′) 2 (wherein R′ represents −CH 3 or −C 2 H 5 , and R″ represents -CH3 ), a silane compound represented by
For example, (CH 3 ) 2 Si(OCH 3 ) 2 (hereinafter referred to as silane C)
This is based on the discovery that the above-mentioned drawbacks of conventional products can be solved by mixing them in a specific ratio. Here, the disadvantages that occur when Silane C is used alone are: (1) The heat-cured film becomes too soft. (2) Heat curing takes a long time. It has been found that these drawbacks can be solved by using the above-mentioned silane A or B in combination. In the present invention, the mixing ratio of silane A or silane B and silane C is preferably in the range of 9:1 to 1:9 by weight. This is not preferable because it causes defects. [Example] The present invention will be explained in more detail below with reference to Examples. Example 1 A mixture of silane A and silane C (composition ratio shown in Table 1 below) was added to 30 g of pure water in which 3 g of acetic acid was dissolved.
g was added thereto and reacted at room temperature for 5 to 15 minutes to obtain a partially hydrolyzed silane compound. Next, a 250% aqueous solution of colloidal silica (containing 21wt% as SiO 2 ) was added to this.
g was added and reacted at room temperature for 5 to 30 minutes to obtain an inorganic composition binder. In addition, the average particle size is about 20μ
400g of silica powder, 100g of silica powder of about 10μm
g and 100 g of alumina powder (average particle size of about 5 μm) were added together with 50 g of methanol, and the mixture was allowed to stand for 2 to 4 days to obtain inorganic slurry compositions Nos. 1 to 7. We evaluated the stability of the slurry, the curing speed of the coating film (coating approximately 2 mm thick on a steel plate, drying at room temperature for 12 hours, and curing at 160°C), heat resistance, and appearance observation (presence of cracks, etc.). I went. The results are shown in Table 1. Example 2 Inorganic slurry compositions Nos. 8 to 13 were obtained in the same manner as in Example 1 except that Silane B was used in place of Silane A in Example 1. The stability, curability, and cured coating properties of this slurry were evaluated, and the results are shown in Table 2. As is clear from Examples 1 and 2, the partially hydrolyzed silanes were mixtures of silane A/silane C and silane B/silane C in a weight ratio of 9/9.
By using one having a ratio of 1 to 1/9, an inorganic composition binder with well-balanced properties and an inorganic slurry composition using the same can be obtained. Example 3 An inorganic binder composition that is a reaction product of the hydrolysis product of the silane A/silane B mixture (1/1 weight ratio) used in inorganic slurry composition No. 4 of Example 1 and colloidal silica. When we coated an iron plate with only the material (without powders such as silica and alumina), a transparent, uniform, continuous film was formed. When this is heated at 160℃ for 20 minutes to harden it,
Even when heated to 600℃, the coating did not crack, peel, or discolor, and a coating with excellent heat resistance was obtained. Further, this film did not peel or crack even after being immersed in boiling water for 1 hour, and maintained its water repellency. Moreover, no change occurred even when immersed in organic solvents such as tricrene, alcohol, and gasoline for one week at room temperature, and the material had excellent heat resistance, boiling water resistance, and chemical resistance.

【表】【table】

【表】 あり、×は撥水性が失われたことを示す。
[Table] Yes, × indicates loss of water repellency.

Claims (1)

【特許請求の範囲】 1 部分加水分解したシラン化合物とコロイダル
シリカの反応生成物をバインダーとし、これに無
機粉体を加えてなる水または水と低級アルコール
混合物系スラリー状組成物において、シラン化合
物として下記一般式 RSi(OR′)3 (式中、Rは−CH3または 【式】 を表し、そしてR′は−CH3または−C2H5を表す)
で示される化合物、及び下記の一般式 R″2Si(OR′)2 (式中、R′は−CH3または−C2H5を表し、そし
てR″は−CH3を表す)で示される化合物を9:
1〜1:9(重量比)で混合して用いることを特
徴とする無機系組成物バインダー。
[Scope of Claims] 1. In a slurry composition based on water or a mixture of water and lower alcohol, which is made by using a reaction product of a partially hydrolyzed silane compound and colloidal silica as a binder and adding an inorganic powder to this, as a silane compound. The following general formula RSi(OR') 3 (in the formula, R represents -CH 3 or [formula], and R' represents -CH 3 or -C 2 H 5 )
and the following general formula R″ 2 Si(OR′) 2 (wherein R′ represents −CH 3 or −C 2 H 5 and R″ represents −CH 3 ). 9 compounds:
An inorganic composition binder characterized in that it is used by mixing at a ratio of 1 to 1:9 (weight ratio).
JP7271585A 1985-04-08 1985-04-08 Inorganic composition binder Granted JPS61233065A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7271585A JPS61233065A (en) 1985-04-08 1985-04-08 Inorganic composition binder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7271585A JPS61233065A (en) 1985-04-08 1985-04-08 Inorganic composition binder

Publications (2)

Publication Number Publication Date
JPS61233065A JPS61233065A (en) 1986-10-17
JPH0369384B2 true JPH0369384B2 (en) 1991-10-31

Family

ID=13497323

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7271585A Granted JPS61233065A (en) 1985-04-08 1985-04-08 Inorganic composition binder

Country Status (1)

Country Link
JP (1) JPS61233065A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01172473A (en) * 1987-12-28 1989-07-07 Toshiba Silicone Co Ltd Coating composition
US5985790A (en) * 1994-12-07 1999-11-16 Project Earth Industries, Inc. Method of making acid contacted enhanced aluminum oxide adsorbent particle
US6342191B1 (en) 1994-12-07 2002-01-29 Apyron Technologies, Inc. Anchored catalyst system and method of making and using thereof
US5948726A (en) * 1994-12-07 1999-09-07 Project Earth Industries, Inc. Adsorbent and/or catalyst and binder system and method of making therefor
US5955393A (en) * 1995-04-21 1999-09-21 Project Earth Industries, Inc. Enhanced adsorbent and room temperature catalyst particle and method of making therefor
KR100381717B1 (en) * 1995-12-29 2003-08-14 고려화학 주식회사 Method for preparing ceramic binder
JP5393107B2 (en) * 2007-12-25 2014-01-22 日東電工株式会社 Silicone resin composition
JP6227700B2 (en) * 2016-04-18 2017-11-08 株式会社トウペ Silicone resin composition and painted product

Also Published As

Publication number Publication date
JPS61233065A (en) 1986-10-17

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