JPH08311330A - Room temperature-curable composition - Google Patents

Room temperature-curable composition

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Publication number
JPH08311330A
JPH08311330A JP11829795A JP11829795A JPH08311330A JP H08311330 A JPH08311330 A JP H08311330A JP 11829795 A JP11829795 A JP 11829795A JP 11829795 A JP11829795 A JP 11829795A JP H08311330 A JPH08311330 A JP H08311330A
Authority
JP
Japan
Prior art keywords
cement
room temperature
curable composition
reactive silicon
pts
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
JP11829795A
Other languages
Japanese (ja)
Other versions
JP3222036B2 (en
Inventor
Junichi Honda
淳一 本多
Yukihiko Murayama
之彦 村山
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP11829795A priority Critical patent/JP3222036B2/en
Publication of JPH08311330A publication Critical patent/JPH08311330A/en
Application granted granted Critical
Publication of JP3222036B2 publication Critical patent/JP3222036B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE: To obtain the subject composition having excellent durability to inva sion of rain water or temperature variation, etc., after curing, comprising a specific proportions of an organopolymer having a reactive silicon, a curing catalyst and cement. CONSTITUTION: This composition comprises (A) 100 pts.wt. of an organopolymer containing a reactive silicon, (B) 0.5-5 pts.wt. of a curing catalyst (e.g.; alkyltitanate) and (C) 10-150 pts.wt. of cement (e.g.; dolomite.plaster). The molecular weight of the component A is preferably 500-50000. In the case where the objective composition is preferably a liquid from the viewpoint of handling, the molecular weight of the component A is preferably 1000-20000. The composition may be blended as necessary with a dehydrating agent such as vinyl methoxysilane or an adhesion-imparting agent such as γ-aminopropyl triethoxysilane. Furthermore, an inorganic granular material such ass silica or an inorganic fibrous material such as sepiolite may be used for the purpose of reinforcing or imparting a thixotropy.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、室温硬化性組成物に関
する。
FIELD OF THE INVENTION This invention relates to room temperature curable compositions.

【0002】[0002]

【従来の技術】反応性けい素基を含有する有機重合体
は、室温下で大気中の湿気と反応して可とう性及び耐衝
撃性に優れるゴム状物質に硬化するので、建築用のシー
リング材、弾性接着剤等として広く用いられている。建
材の目地部分をシーリング材で保護するシーリング工事
では、シーリング材を充填した後、表面を平滑にするた
めにシーリング材の硬化前にヘラ仕上げが行われる。こ
の場合、シーリング材が硬化するとヘラ仕上げが困難に
なるため、シーリング材が硬化するのが遅いほど作業性
がよくなるが、その一方では、目地の動きに対応できる
点、埃の付着による表面の汚染等の点から、シーリング
材はできるだけ速く硬化することが望まれる。
2. Description of the Related Art An organic polymer containing a reactive silicon group reacts with atmospheric humidity at room temperature to be cured into a rubber-like substance having excellent flexibility and impact resistance. Widely used as materials, elastic adhesives, etc. In a sealing work for protecting joints of a building material with a sealing material, a spatula finish is performed after the sealing material is filled and before the sealing material is cured in order to smooth the surface. In this case, since the spatula finish becomes difficult when the sealing material hardens, the slower the sealing material cures, the better the workability. On the other hand, on the other hand, the point that it can respond to the movement of the joint and the contamination of the surface by the adhesion of dust Therefore, it is desired that the sealing material be cured as quickly as possible.

【0003】特開平3−294355号公報には、ポリ
アルキレンエーテル、有機けい素化合物、充填剤及びシ
ラノール触媒からなる室温硬化性組成物が、シーリング
材、弾性接着剤等として有用である旨が開示されてい
る。
JP-A-3-294355 discloses that a room-temperature-curable composition comprising a polyalkylene ether, an organic silicon compound, a filler and a silanol catalyst is useful as a sealing material, an elastic adhesive or the like. Has been done.

【0004】このような室温硬化性組成物が、シーリン
グ材、弾性接着剤等として使用される場合、硬化後も屋
外の環境にさらされ、雨水の浸入、温度変化等により接
着強度が低下するため、耐久性が充分であるとはいえな
かった。
When such a room temperature curable composition is used as a sealing material, an elastic adhesive, etc., it is exposed to the outdoor environment even after curing, and the adhesive strength is lowered due to the infiltration of rainwater, temperature change, etc. However, the durability was not sufficient.

【0005】[0005]

【発明が解決しようとする課題】本発明は、上記に鑑
み、硬化後の雨水の浸入、温度変化等に対して良好な耐
久性を有する室温硬化性組成物を提供することを目的と
する。
SUMMARY OF THE INVENTION In view of the above, it is an object of the present invention to provide a room temperature curable composition having good durability against infiltration of rainwater after curing, temperature change and the like.

【0006】[0006]

【課題を解決するための手段】本発明の要旨は、室温硬
化性組成物を、反応性けい素基を含有する有機重合体1
00重量部、硬化触媒0.5〜5重量部、及び、セメン
ト10〜150重量部から構成するところに存する。
DISCLOSURE OF THE INVENTION The gist of the present invention is to provide a room temperature curable composition containing an organic polymer 1 containing a reactive silicon group.
It is composed of 100 parts by weight, 0.5 to 5 parts by weight of a curing catalyst, and 10 to 150 parts by weight of cement.

【0007】本発明で使用される反応性けい素基を含有
する有機重合体としては特に限定されず、例えば、下記
の一般式 −R−O− (式中、Rは、炭素数2〜4の2価のアルキレン基を表
す)で示される繰り返し単位を有するポリエーテル;ポ
リプロピレンオキシド等のポリエーテルの存在下でアク
リル酸エステル、スチレン、アクリロニトリル、酢酸ビ
ニル等のビニルモノマーを重合させて得られるグラフト
重合体等の重合体又は共重合体;ポリアクリル酸アルキ
ルエステル又はアクリル酸アルキルエステルを50%以
上含有するアクリル酸アルキルエステルと酢酸ビニル、
アクリロニトリル、スチレン、エチレン等との共重合体
等が挙げられる。これらは単独で使用してもよく、2種
以上を併用してもよい。
The organic polymer containing a reactive silicon group used in the present invention is not particularly limited, and for example, the following general formula --RO-- (wherein R is a carbon number of 2 to 4) is used. A divalent alkylene group), which is a graft unit obtained by polymerizing a vinyl monomer such as acrylate ester, styrene, acrylonitrile or vinyl acetate in the presence of a polyether such as polypropylene oxide. Polymers or copolymers such as polymers; polyacrylic acid alkyl ester or acrylic acid alkyl ester containing 50% or more of acrylic acid alkyl ester and vinyl acetate,
Examples thereof include copolymers with acrylonitrile, styrene, ethylene and the like. These may be used alone or in combination of two or more.

【0008】本明細書において反応性けい素とは、水酸
基又は加水分解性基が結合したけい素原子含有基であっ
て、シラノール縮合反応によりシロキサン結合を形成で
きる基のことである。上記加水分解性基としては特に限
定されず、例えば、メトキシ基、エトキシ基等の反応性
が穏やかであるアルコキシ基等が挙げられる。
In the present specification, the reactive silicon means a silicon atom-containing group to which a hydroxyl group or a hydrolyzable group is bonded and which can form a siloxane bond by a silanol condensation reaction. The hydrolyzable group is not particularly limited, and examples thereof include alkoxy groups having mild reactivity such as methoxy group and ethoxy group.

【0009】上記反応性けい素基を含有する有機重合体
の分子量は、500〜50000が好ましい。取り扱い
の点から室温硬化性組成物が液状であることが好ましい
場合、分子量は、1000〜20000が好ましい。
The molecular weight of the organic polymer having a reactive silicon group is preferably 500 to 50,000. When the room temperature curable composition is preferably liquid in terms of handling, the molecular weight is preferably 1,000 to 20,000.

【0010】本発明で使用される硬化触媒としては特に
限定されず、例えば、アルキルチタン酸塩、有機けい素
チタン酸塩、オクチル酸すず、ジブチルすずジラウレー
ト、ジブチルすずマレート、ジブチルすずフタレート等
のカルボン酸金属塩;ジブチルアミン−2−エチルヘキ
ソエート等のアミン塩;その他の酸性触媒及び塩基性触
媒等の公知のシラノール縮合触媒等が挙げられる。これ
らは単独で使用してもよく、2種以上を併用してもよ
い。
The curing catalyst used in the present invention is not particularly limited, and examples thereof include alkyl titanates, organosilicon titanates, tin octylates, dibutyltin dilaurates, dibutyltin malates, dibutyltin phthalates, and other carboxylic acids. Examples thereof include acid metal salts; amine salts such as dibutylamine-2-ethylhexoate; and other known silanol condensation catalysts such as acidic catalysts and basic catalysts. These may be used alone or in combination of two or more.

【0011】上記硬化触媒の添加量は、上記反応性けい
素基を含有する有機重合体100重量部に対し、0.5
〜5重量部である。0.5重量部未満であると、硬化促
進の充分な効果が得られず、5重量部を超えると、触媒
効果の向上が見られず、希釈作用が出るので、上記範囲
に限定される。
The amount of the curing catalyst added is 0.5 with respect to 100 parts by weight of the organic polymer containing a reactive silicon group.
~ 5 parts by weight. If it is less than 0.5 parts by weight, a sufficient effect of accelerating the curing cannot be obtained, and if it exceeds 5 parts by weight, the catalytic effect is not improved and a diluting action is exerted, so that it is limited to the above range.

【0012】本発明で使用されるセメントとしては特に
限定されず、例えば、ドロマイト・プラスター、キーン
スセメント、マグネシアセメント等の気硬性セメント;
ローマンセメント、天然セメント、ポルトランドセメン
ト、アルミナセメント、高炉セメント、シリカ・セメン
ト、フライ・アッシュ・セメント、メーソンリー・セメ
ント、膨張性セメント、着色セメント等の水硬性セメン
ト;耐酸セメント等の特殊セメント等が挙げられる。こ
れらは単独で使用してもよく、2種以上を併用してもよ
い。
The cement used in the present invention is not particularly limited, and examples thereof include air-hardening cements such as dolomite plaster, keens cement and magnesia cement;
Roman cement, natural cement, Portland cement, alumina cement, blast furnace cement, silica cement, fly ash cement, masonry cement, expansive cement, hydraulic cement such as colored cement; special cement such as acid resistant cement Can be mentioned. These may be used alone or in combination of two or more.

【0013】上記セメントの添加量は、上記反応性けい
素基を含有する有機重合体100重量部に対し、10〜
150重量部である。10重量部未満であると、被着体
及び外部から室温硬化性組成物中に浸入してくる水を充
分吸収できないため、接着耐久性の向上に充分な効果が
得られず、150重量部を超えると、吸収した水により
セメントが硬化し、室温硬化性組成物の可とう性が損な
われ、シーリング材、弾性接着剤等の特徴であるゴム弾
性が失われるので、上記範囲に限定される。
The cement is added in an amount of 10 to 100 parts by weight of the organic polymer containing the reactive silicon group.
It is 150 parts by weight. If the amount is less than 10 parts by weight, water that permeates into the room temperature curable composition from the adherend and the outside cannot be sufficiently absorbed, and therefore, sufficient effect for improving the adhesion durability cannot be obtained. When it exceeds, the cement is hardened by the absorbed water, the flexibility of the room temperature curable composition is impaired, and the rubber elasticity which is a characteristic of the sealing material, the elastic adhesive and the like is lost, so the content is limited to the above range.

【0014】本発明の室温硬化性組成物には、必要に応
じて、脱水剤、接着性付与剤等を配合していてもよい。
If necessary, the room temperature curable composition of the present invention may contain a dehydrating agent, an adhesiveness-imparting agent or the like.

【0015】上記脱水剤としては特に限定されず、例え
ば、ビニルトリメトキシシラン等のビニルシラン類;オ
ルソぎ酸エステル等が挙げられる。本発明の室温硬化性
組成物の必須成分である反応性けい素基を含有する有機
重合体は、水分により硬化反応が進行してしまうため、
微量の水分により配合物が使用前にゲル化するのを防止
するため、脱水剤を添加しておくことが好ましい。
The dehydrating agent is not particularly limited, and examples thereof include vinylsilanes such as vinyltrimethoxysilane; orthoformate ester and the like. The organic polymer containing a reactive silicon group which is an essential component of the room temperature curable composition of the present invention, the curing reaction proceeds due to moisture,
A dehydrating agent is preferably added in order to prevent the compound from gelling before use due to a trace amount of water.

【0016】上記接着性付与剤としては特に限定され
ず、例えば、(2−アミノエチル)アミノプロピルトリ
メトキシシラン、γ−アミノプロピルトリエトキシシラ
ン等のアミノシラン類;γ−メルカプトプロピルトリメ
トキシシラン等のメルカプトシラン類;γ−グリシドキ
シプロピルトリメトキシシラン等のエポキシシラン類等
が挙げられる。
The adhesiveness imparting agent is not particularly limited, and examples thereof include aminosilanes such as (2-aminoethyl) aminopropyltrimethoxysilane and γ-aminopropyltriethoxysilane; γ-mercaptopropyltrimethoxysilane and the like. Mercaptosilanes; epoxysilanes such as γ-glycidoxypropyltrimethoxysilane and the like.

【0017】本発明の室温硬化性組成物の補強及び揺変
性付与を目的として、例えば、炭酸カルシウム、炭酸マ
グネシウム、含水けい酸、けい酸カルシウム、シリカ、
二酸化チタン、クレー、タルク等の無機粒状物;アスベ
スト、ウォラストナイト、セピオライト、スラグ繊維、
ゾノトライト、チタン酸カリウム、エレスタダイト、石
膏繊維等の無機繊維状物;水添化ひまし油、脂肪酸アマ
イドワックス等の有機系揺変剤、マイカ、カオリン、ベ
ントナイト等の無機鉱物;ガラスバルン、フライアッシ
ュバルン、シラスバルン等の中空状充填剤等を使用して
もよい。
For the purpose of reinforcing and imparting thixotropy to the room temperature curable composition of the present invention, for example, calcium carbonate, magnesium carbonate, hydrous silicic acid, calcium silicate, silica,
Inorganic particles such as titanium dioxide, clay, talc; asbestos, wollastonite, sepiolite, slag fiber,
Inorganic fibrous substances such as zonotolite, potassium titanate, elestadite, gypsum fibers; hydrogenated castor oil, organic thixotropic agents such as fatty acid amide wax, inorganic minerals such as mica, kaolin and bentonite; glass balun, fly ash balun, silas balun You may use hollow filler etc.

【0018】上記のほか、フタル酸エステル等の可塑
剤;ヒンダードアミン系、ヒンダードフェノール系等の
老化防止剤;カーボンブラック等の顔料;紫外線吸収剤
等を添加してもよい。
In addition to the above, a plasticizer such as a phthalate ester; an antiaging agent such as a hindered amine type or a hindered phenol type; a pigment such as carbon black; an ultraviolet absorber or the like may be added.

【0019】[0019]

【実施例】以下に実施例を掲げて本発明を更に詳しく説
明するが、本発明はこれら実施例のみに限定されるもの
ではない。
The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.

【0020】室温硬化性組成物の調製 実施例1〜5、比較例1〜3について、表1に示す重量
比で各原料を計量し、密封した混合攪拌機内で均一に混
練し室温硬化性組成物を調製した。上述のようにして調
製した実施例1〜5及び比較例1〜3の各組成物につい
て、下記の評価を行った。
Preparation of Room Temperature Curable Compositions For Examples 1 to 5 and Comparative Examples 1 to 3, the respective raw materials were weighed at the weight ratios shown in Table 1 and uniformly kneaded in a sealed mixing stirrer to obtain room temperature curable compositions. The thing was prepared. The following evaluations were performed on the compositions of Examples 1 to 5 and Comparative Examples 1 to 3 prepared as described above.

【0021】接着性 JIS K 6852(接着剤の圧縮剪断接着強さ試験
法)に従い、被着体として磁器質モザイクタイル及びモ
ルタルを用いて、上述した方法で調製した室温硬化性組
成物を1.5kg/m2 の割合になるように塗布した後
(接着面積25mm×25mm)、両被着体を貼り合わ
せた。この試験体を温度23℃、湿度65%の恒温恒湿
室で14日間養生した後、圧縮剪断試験を行った。更
に、養生した試験体を90℃の熱水に1ヵ月浸漬し、温
度60℃で8時間真空乾燥した後、同様の圧縮剪断試験
を行った。
Adhesiveness: According to JIS K 6852 (compressive shear adhesive strength test method for adhesives), using a porcelain mosaic tile and mortar as adherends, the room temperature curable composition prepared by the above-mentioned method was used. After coating so as to have a rate of 5 kg / m 2 (bonding area 25 mm × 25 mm), both adherends were bonded together. This test body was aged in a constant temperature and humidity room at a temperature of 23 ° C. and a humidity of 65% for 14 days and then subjected to a compression shear test. Further, the cured test body was immersed in hot water at 90 ° C. for 1 month and vacuum dried at a temperature of 60 ° C. for 8 hours, and then the same compression shear test was performed.

【0022】硬化物物性 調製した室温硬化性組成物を厚さ2mmのシート状に展
延し、温度23℃、湿度65%の恒温恒湿室で14日間
養生、硬化させた後、JIS K 6301(架硫ゴム
物理試験法)に従い3号ダンベル形状にて、抗張力及び
伸び率を測定した。また、養生した硬化物を90℃の熱
水に1ヵ月浸漬し、温度60℃で8時間真空乾燥した
後、同様に抗張力及び伸び率を測定した。結果を表1に
示す。
Physical Properties of Cured Material The prepared room temperature curable composition was spread into a sheet having a thickness of 2 mm, cured and cured in a constant temperature and humidity room at a temperature of 23 ° C. and a humidity of 65% for 14 days, and then JIS K 6301 was used. According to (Physical test method for vulcanized rubber), tensile strength and elongation were measured with a No. 3 dumbbell shape. Moreover, the cured product was immersed in hot water at 90 ° C. for 1 month and vacuum-dried at a temperature of 60 ° C. for 8 hours, and then the tensile strength and the elongation were measured in the same manner. The results are shown in Table 1.

【0023】実施例1〜5、比較例1〜3の原材料の内
容は以下の通りである。 (1)反応性けい素基を含有する有機重合体;(鐘淵化
学工業社製、サイリルSAT200) (2)反応性けい素基を含有する有機重合体;(鐘淵化
学工業社製、サイリルMAX447) (3)コロイド炭酸カルシウム;(白石工業社製、CC
R) (4)疎水性シリカ;(日本アエロジル社製、アエロジ
ルR202) (5)ポルトランドセメント;(秩父小野田セメント社
製) (6)アルミナセメント;(旭硝子社製) (7)γ−(2−アミノエチル)アミノプロピルトリメ
トキシシラン;(信越シリコーン社製、KBM603) (8)ビニルトリメトキシシラン;(信越シリコーン社
製、KBM1003) (9)反応性けい素基を含有する有機重合体の硬化触
媒;ジブチルすずジアセチルアセトナート(日東化成社
製、ネオスタンU−220)
The contents of the raw materials of Examples 1 to 5 and Comparative Examples 1 to 3 are as follows. (1) Organic polymer containing reactive silicon group; (Kanefuchi Chemical Industry Co., Ltd., Cyryl SAT200) (2) Organic polymer containing reactive silicon group; (Kanebuchi Chemical Industry Co., Ltd., Cyryl (MAX447) (3) Colloidal calcium carbonate; (manufactured by Shiraishi Industry Co., Ltd., CC
R) (4) Hydrophobic silica; (Aerosil R202 manufactured by Nippon Aerosil Co., Ltd.) (5) Portland cement; (Chichibu Onoda Cement Co., Ltd.) (6) Alumina cement; (Asahi Glass Co., Ltd.) (7) γ- (2- (Aminoethyl) aminopropyltrimethoxysilane; (KBM603, manufactured by Shin-Etsu Silicone Co., Ltd.) (8) Vinyltrimethoxysilane; (KBM1003, manufactured by Shin-Etsu Silicone Co., Ltd.) (9) Curing catalyst for organic polymer containing reactive silicon group Dibutyltin diacetylacetonate (Nitostane U-220 manufactured by Nitto Kasei Co., Ltd.)

【0024】表1から明らかなように、本発明の実施例
1〜5の室温硬化性組成物では、良好な接着性及び接着
耐久性を示し、かつ、硬化物が柔軟性を有しているのに
対して、比較例1〜3の室温硬化性組成物では、これら
の物性のいずれか、又は、両者とも満たすことはできな
かった。
As is clear from Table 1, the room temperature curable compositions of Examples 1 to 5 of the present invention show good adhesiveness and adhesion durability, and the cured products have flexibility. On the other hand, the room temperature curable compositions of Comparative Examples 1 to 3 could not satisfy either or both of these physical properties.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【発明の効果】本発明の室温硬化性組成物は上述の構成
よりなるので、硬化後の雨水の浸入、温度変化等に対し
て良好な耐久性を有する室温硬化性組成物を得ることが
できる。
EFFECTS OF THE INVENTION Since the room temperature curable composition of the present invention has the above-mentioned constitution, it is possible to obtain a room temperature curable composition having good durability against infiltration of rainwater after curing, temperature change and the like. .

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 反応性けい素基を含有する有機重合体1
00重量部、硬化触媒0.5〜5重量部、及び、セメン
ト10〜150重量部からなることを特徴とする室温硬
化性組成物。
1. An organic polymer 1 containing a reactive silicon group.
A room temperature curable composition comprising 00 parts by weight, 0.5 to 5 parts by weight of a curing catalyst, and 10 to 150 parts by weight of cement.
JP11829795A 1995-05-17 1995-05-17 Room temperature curable composition Expired - Lifetime JP3222036B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11829795A JP3222036B2 (en) 1995-05-17 1995-05-17 Room temperature curable composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11829795A JP3222036B2 (en) 1995-05-17 1995-05-17 Room temperature curable composition

Publications (2)

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JPH08311330A true JPH08311330A (en) 1996-11-26
JP3222036B2 JP3222036B2 (en) 2001-10-22

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004277751A (en) * 2004-05-18 2004-10-07 Cemedine Co Ltd Moisture-curable adhesive composition having excellent transparency
WO2011087073A1 (en) * 2010-01-18 2011-07-21 日本ジッコウ株式会社 Silicone resin composition and protective coating method using silicone resin composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004277751A (en) * 2004-05-18 2004-10-07 Cemedine Co Ltd Moisture-curable adhesive composition having excellent transparency
WO2011087073A1 (en) * 2010-01-18 2011-07-21 日本ジッコウ株式会社 Silicone resin composition and protective coating method using silicone resin composition
JP5710503B2 (en) * 2010-01-18 2015-04-30 日本ジッコウ株式会社 Silicone resin composition and protective coating method using silicone resin composition

Also Published As

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