[go: up one dir, main page]

JP3022124B2 - Room temperature curable organopolysiloxane composition - Google Patents

Room temperature curable organopolysiloxane composition

Info

Publication number
JP3022124B2
JP3022124B2 JP5351844A JP35184493A JP3022124B2 JP 3022124 B2 JP3022124 B2 JP 3022124B2 JP 5351844 A JP5351844 A JP 5351844A JP 35184493 A JP35184493 A JP 35184493A JP 3022124 B2 JP3022124 B2 JP 3022124B2
Authority
JP
Japan
Prior art keywords
parts
weight
group
composition
curable organopolysiloxane
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 - Fee Related
Application number
JP5351844A
Other languages
Japanese (ja)
Other versions
JPH07188560A (en
Inventor
敬 三好
徳夫 佐藤
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP5351844A priority Critical patent/JP3022124B2/en
Publication of JPH07188560A publication Critical patent/JPH07188560A/en
Application granted granted Critical
Publication of JP3022124B2 publication Critical patent/JP3022124B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

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、建築産業分野等におい
て、建築材料等として有用な室温硬化性オルガノポリシ
ロキサン組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a room-temperature-curable organopolysiloxane composition useful as a building material in the construction industry.

【0002】[0002]

【従来の技術】室温硬化性オルガノポリシロキサン組成
物は、得られる硬化物が耐候性、耐熱性等の特性を有す
ることより、建築産業分野をはじめ様々な分野に応用さ
れてきた。近年、建築産業分野においては、かかる特性
はもとより、硬化物の外観が重視されるようになってき
た。しかし、室温硬化性オルガノポリシロキサン組成物
は、主成分であるオルガノポリシロキサンの表面エネル
ギーが低いために、通常使用される組成では、得られる
硬化物の表面が艶ありにしかならなかった。従って、こ
のような組成物は艶消し表面が要求される箇所に使用す
ることができなかった。
2. Description of the Related Art Room temperature-curable organopolysiloxane compositions have been applied to various fields including the construction industry since the resulting cured products have properties such as weather resistance and heat resistance. In recent years, in the field of the construction industry, emphasis has been placed on the appearance of cured products, in addition to such properties. However, in the case of a room temperature-curable organopolysiloxane composition, the surface energy of the organopolysiloxane, which is the main component, is low, and the surface of the resulting cured product is only glossy with a commonly used composition. Therefore, such compositions could not be used where a matte surface was required.

【0003】そこで、表面が艶消しである硬化物を与え
る室温硬化性オルガノポリシロキサン組成物を調製する
技術として、粒子の粗い無機充填材を組成物に大量に含
有させる技術が提案された。しかし、これでは得られる
組成物の比重が大きくなる、組成物の押し出し性が著し
く低下する、得られる硬化物の伸び等の機械的物性が低
下する等の欠点がある。この欠点のため、この技術によ
り得られる組成物は、得られる硬化物の表面が艶消しで
あるものの、限られた用途にしか応用されていなかっ
た。
Accordingly, as a technique for preparing a room-temperature-curable organopolysiloxane composition that gives a cured product having a matte surface, a technique has been proposed in which a large amount of an inorganic filler having coarse particles is contained in the composition. However, this has disadvantages such as an increase in the specific gravity of the obtained composition, a remarkable decrease in the extrudability of the composition, and a decrease in mechanical properties such as elongation of the obtained cured product. Due to this drawback, the composition obtained by this technique has been applied only to limited uses, although the cured product obtained has a matte surface.

【0004】[0004]

【発明が解決しようとする課題】そこで、本発明の課題
は、比重が特に大きくなく、良好な機械的物性を有しな
がら表面が艶消しである硬化物を与える室温硬化性オル
ガノポリシロキサン組成物を提供することである。
SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a room temperature curable organopolysiloxane composition which has a specific gravity which is not particularly large and which gives a cured product having a matte surface while having good mechanical properties. It is to provide.

【0005】[0005]

【課題を解決するための手段】本発明は、上記課題を解
決するものとして、 (a) 分子鎖両末端が水酸基で停止されたジオルガノポリシロキサン 100重量部、 (b) 一分子中にけい素原子に結合した加水分解性基を少なくとも3個有する有 機けい素化合物及びその部分加水分解物からなる群より選ばれる少なくとも一種 0.5〜30重量部、 (c) 無機充填剤 1〜500重量部、 及び (d) 繊維長が0.01〜0.5mmである繊維状樹脂 0.1〜20重量部 を含有してなるオルガノポリシロキサン組成物を提供す
る。以下、本発明を詳細に説明する。
The present invention solves the above-mentioned problems by providing (a) 100 parts by weight of a diorganopolysiloxane in which both ends of a molecular chain are terminated by hydroxyl groups, and (b) silicon in one molecule. At least one selected from the group consisting of an organic silicon compound having at least three hydrolyzable groups bonded to a silicon atom and a partial hydrolyzate thereof; 0.5 to 30 parts by weight; (c) inorganic filler 1 to 500 The present invention provides an organopolysiloxane composition comprising, by weight, 0.1 to 20 parts by weight of a fibrous resin having a fiber length of 0.01 to 0.5 mm. Hereinafter, the present invention will be described in detail.

【0006】(a) 成分 (a) 成分としては、例えば、下記一般式(1) : (式中、R1 は、同一でも異なってもよく、置換又は非
置換の一価炭化水素基であり、nは10以上の整数であ
る)で表されるジオルガノポリシロキサンが挙げられ
る。一般式(1) において、置換又は非置換の一価炭化水
素基R1 としては、例えば、メチル基、エチル基、プロ
ピル基等のアルキル基;シクロヘキシル基等のシクロア
ルキル基;ビニル基、アリル基等のアルケニル基;フェ
ニル基、トリル基等のアリール基;これら炭化水素基の
水素原子が部分的にフッ素等のハロゲン原子等で置換さ
れた基等が挙げられる。
(A) Component As the component (a), for example, the following general formula (1): (Wherein R 1 may be the same or different and is a substituted or unsubstituted monovalent hydrocarbon group, and n is an integer of 10 or more). In the general formula (1), examples of the substituted or unsubstituted monovalent hydrocarbon group R 1 include an alkyl group such as a methyl group, an ethyl group and a propyl group; a cycloalkyl group such as a cyclohexyl group; a vinyl group and an allyl group Alkenyl group such as phenyl group, tolyl group and the like; groups in which hydrogen atoms of these hydrocarbon groups are partially substituted by halogen atoms such as fluorine and the like.

【0007】上記オルガノポリシロキサンの粘度は、2
5℃で25〜500,000cStの範囲内であること
が好ましく、より好ましくは25℃で1,000〜10
0,000cStの範囲内である。
The viscosity of the organopolysiloxane is 2
It is preferably within the range of 25 to 500,000 cSt at 5 ° C, more preferably 1,000 to 10 at 25 ° C.
It is in the range of 000 cSt.

【0008】(b) 成分 (b) 成分の有機けい素化合物としては、例えば、シラ
ン、シロキサン等が挙げられる。該有機けい素化合物が
含有する加水分解性基としては、例えば、メトキシ基、
エトキシ基等のアルコキシ基;ジメチルケトオキシム
基、メチルエチルケトオキシム基等のケトオキシム基;
アセトキシ基等のアシルオキシ基;N−ブチルアミノ
基、N,N−ジエチルアミノ基等のアミノ基;N−メチ
ルアセトアミド基等のアミド基;N,N−ジメチルアミ
ノキシ基、N,N−ジエチルアミノキシ基等のアミノキ
シ基;イソプロぺノキシ基、イソブテノキシ基、シクロ
ヘキセノキシ基等のアルケニルオキシ基等が挙げられ
る。
(B) Component The organosilicon compound as the component (b) includes, for example, silane, siloxane and the like. Examples of the hydrolyzable group contained in the organosilicon compound include, for example, a methoxy group,
An alkoxy group such as an ethoxy group; a ketoxime group such as a dimethyl ketoxime group and a methyl ethyl ketoxime group;
Acyloxy groups such as acetoxy group; amino groups such as N-butylamino group and N, N-diethylamino group; amide groups such as N-methylacetamide group; N, N-dimethylaminooxy group and N, N-diethylaminoxy group And an alkenyloxy group such as an isopropenoxy group, an isobutenoxy group and a cyclohexenoxy group.

【0009】この有機けい素化合物の具体例としては、
メチルトリメトキシシラン、ビニルトリエトキシシラ
ン、3−クロロプロピルトリメトキシシラン、3−アミ
ノプロピルトリエトキシシラン等のアルコキシシラン、
メチルトリス(ジメチルケトオキシム)シラン、メチル
トリス(メチルエチルケトオキシム)シラン、ビニルト
リス(メチルエチルケトオキシム)シラン、テトラ(メ
チルエチルケトオキシム)シラン等のケトオキシムシラ
ン、ビニルトリアセトキシシラン、メチルトリアセトキ
シシラン、フェニルトリアセトキシシラン等のアシルオ
キシシラン、フェニルトリス(N−メチルアセトアミ
ド)シラン、ビニルトリス(N−メチルアセトアミド)
シラン等のアミドシラン、ビニルトリス(N−ブチルア
ミノ)シラン、フェニルトリス(N,N−ジエチルアミ
ノ)シラン等のアミノシラン、メチルトリス(N,N−
ジメチルアミノキシ)シラン、ビニルトリス(N,N−
ジエチルアミノキシ)シラン等のアミノオキシシラン、
ビニルトリイソプロペノキシシラン、メチルトリイソブ
テノキシシラン、フェニルトリシクロへキサノキシシラ
ン等のアルケニルオキシシラン等が挙げられる。これら
の有機けい素化合物及びその部分加水分解物は、1種単
独で用いてもよいし2種以上を組合わせて用いてもよ
い。
Specific examples of the organosilicon compound include:
Alkoxysilanes such as methyltrimethoxysilane, vinyltriethoxysilane, 3-chloropropyltrimethoxysilane, 3-aminopropyltriethoxysilane,
Ketoxime silanes such as methyltris (dimethylketoxime) silane, methyltris (methylethylketoxime) silane, vinyltris (methylethylketoxime) silane, tetra (methylethylketoxime) silane, vinyltriacetoxysilane, methyltriacetoxysilane, phenyltriacetoxysilane, etc. Acyloxysilane, phenyltris (N-methylacetamido) silane, vinyltris (N-methylacetamido)
Amidosilanes such as silane, aminosilanes such as vinyltris (N-butylamino) silane and phenyltris (N, N-diethylamino) silane, methyltris (N, N-
Dimethylaminoxy) silane, vinyl tris (N, N-
Aminooxysilanes such as diethylaminoxy) silane,
Alkenyloxysilanes such as vinyltriisopropenoxysilane, methyltriisobutenoxysilane, and phenyltricyclohexanoxysilane are exemplified. These organosilicon compounds and partial hydrolysates thereof may be used alone or in combination of two or more.

【0010】(b) 成分の量は、(a) 成分100重量部当
り、0.5〜30重量部であり、好ましくは3〜20重
量部である。この量が0.5重量部未満であると、組成
物調製時あるいは組成物保存中に組成物がゲル化を起こ
したり、十分な硬化が達成されないので組成物を硬化し
て得られる弾性体の機械的強度が低下したりする。ま
た、30重量部を超えると、組成物の硬化時の収縮率が
大きくなり、得られる硬化物の弾性が抵下する。
The amount of the component (b) is 0.5 to 30 parts by weight, preferably 3 to 20 parts by weight, per 100 parts by weight of the component (a). If this amount is less than 0.5 part by weight, the composition may gel during the preparation of the composition or during storage of the composition, or the curing of the elastic body obtained by curing the composition may not be achieved sufficiently. The mechanical strength is reduced. On the other hand, when the amount exceeds 30 parts by weight, the shrinkage of the composition at the time of curing becomes large, and the elasticity of the obtained cured product decreases.

【0011】(c) 成分 (c) 成分としては、通常、室温硬化性オルガノポリシロ
キサン組成物に添加される無機充填剤でよく、例えば、
煙霧質シリカ、湿式シリカ、コロイダル炭酸カルシウ
ム、重質炭酸カルシウム、炭酸亜鉛、カーボンブラッ
ク、二酸化チタン、酸化アルミニウム、石英粉未、タル
ク、べントナイト等が挙げられる。これら無機充填剤の
表面は、ヘキサメチルジシラザンで疏水化処理あるいは
ステアリン酸石鹸で処理されていてもよい。
Component (c) The component (c) may be an inorganic filler usually added to a room temperature-curable organopolysiloxane composition.
Examples include fumed silica, wet silica, colloidal calcium carbonate, heavy calcium carbonate, zinc carbonate, carbon black, titanium dioxide, aluminum oxide, quartz powder, talc, bentonite and the like. The surface of these inorganic fillers may be subjected to a hydrophobic treatment with hexamethyldisilazane or a treatment with stearic acid soap.

【0012】(c) 成分の量は、(a) 成分100重量部当
り、1〜500重量部であり、好ましくは10〜300
重量部である。この量が1重量部未満であると、組成物
を硬化して得られる弾性体が実用に耐え得る機械的強度
を示さなくなる。また、500重量部を超えると、この
弾性体が脆くなる。
The amount of the component (c) is 1 to 500 parts by weight, preferably 10 to 300 parts by weight, per 100 parts by weight of the component (a).
Parts by weight. If the amount is less than 1 part by weight, the elastic body obtained by curing the composition will not exhibit practically usable mechanical strength. If it exceeds 500 parts by weight, the elastic body becomes brittle.

【0013】(d) 成分 (d) 成分としては、組成物中の各成分に対して不活性で
あればどのような繊維状樹脂であってもよく、例えば、
ポリエチレン、ポリプロピレン、ポリエステル、ナイロ
ン、テトロン等からなる繊維状樹脂が挙げられる。
(D) Component The component (d) may be any fibrous resin as long as it is inert to each component in the composition.
Examples include fibrous resins made of polyethylene, polypropylene, polyester, nylon, tetron and the like.

【0014】(d) 成分の繊維長は0.01〜0.5mm
の範囲内であることが必要である。この繊維長が0.0
1mm未満であると、得られる硬化物の表面を十分に艶
消しの状態にすることができない。また、0.5mmを
超えると、伸び等の機械的物性が極端に低下したり、硬
化物の外観が損なわれたりする。
The fiber length of the component (d) is 0.01 to 0.5 mm
Must be within the range. This fiber length is 0.0
If it is less than 1 mm, the surface of the obtained cured product cannot be sufficiently matted. On the other hand, when the thickness exceeds 0.5 mm, mechanical properties such as elongation are extremely reduced, and the appearance of the cured product is impaired.

【0015】(d) 成分の量は、(a) 成分100重量部当
り、0.1〜20重量部であり、好ましくは0.5〜1
0重量部である。この量が0.1重量部未満であると、
得られる硬化物の表面を十分に艶消しの状態にすること
ができない。また、20重量部を超えると、引張強さ、
伸び等の機械的物性が極端に低下したり、硬化物の外観
が損なわれたりする。
The amount of the component (d) is 0.1 to 20 parts by weight, preferably 0.5 to 1 part by weight, per 100 parts by weight of the component (a).
0 parts by weight. If this amount is less than 0.1 parts by weight,
The surface of the obtained cured product cannot be sufficiently matted. Also, if it exceeds 20 parts by weight, the tensile strength,
The mechanical properties such as elongation are extremely reduced, and the appearance of the cured product is impaired.

【0016】その他の添加剤 本発明のオルガノポリシロキサン組成物には、必要に応
じて、縮合硬化性の室温硬化型オルガノポリシロキサン
組成物に通常添加される公知の添加物、例えば、アミ
ン、第4級アンモニウム塩、ジブチルスズジオクトエー
ト等の有機金属化合物、チタンキレート化合物、グアニ
ジル基含有化合物等の硬化触媒〔通常、(a) 成分100
重量部当り0.05〜10重量部〕;メタクリル酸カリ
ウム等の対油性向上剤;着色剤;ベンガラ、酸化セリウ
ム等の耐熱性向上剤;耐寒性向上剤;ポリエーテル等の
チクソトロピー剤;脱水剤;γ−アミノプロピルトリエ
トキシシラン等の接着性向上剤等を添加してもよい。
Other Additives The organopolysiloxane composition of the present invention may contain , if necessary, known additives usually added to the condensation-curable room temperature-curable organopolysiloxane composition, such as amines, Curing catalysts such as organic metal compounds such as quaternary ammonium salts and dibutyltin dioctoate, titanium chelate compounds, and guanidyl group-containing compounds [usually, component (a) 100
0.05 to 10 parts by weight per part by weight]; an oil-resistance improving agent such as potassium methacrylate; a coloring agent; a heat resistance improving agent such as red iron oxide and cerium oxide; a cold resistance improving agent; a thixotropic agent such as polyether; An adhesiveness improver such as γ-aminopropyltriethoxysilane may be added.

【0017】組成物の調製 本発明の組成物は、例えば、(a) 〜(d) 成分の所定量を
乾燥(即ち、無水の)雰囲気中で均一に混合することに
より一液型の組成物として調製される。また、例えば、
(a) 、(c) 及び(d) 成分の均一混合物と(b) 成分とを各
々別包装とした二液型の組成物として調製してもよい。
本発明の組成物は、組成物を大気中に暴露すると、大気
中の湿分によって組成物が硬化する。
Preparation of Composition The composition of the present invention can be prepared , for example, by mixing a predetermined amount of the components (a) to (d) uniformly in a dry (ie, anhydrous) atmosphere to form a one-part composition. It is prepared as Also, for example,
A homogeneous mixture of the components (a), (c) and (d) and the component (b) may be prepared as a two-pack type composition separately packaged.
When the composition of the present invention is exposed to the atmosphere, the composition is cured by moisture in the atmosphere.

【0018】用途 本発明の室温硬化型のオルガノポリシロキサン組成物
は、例えば、建築材料の外観が重要視される箇所等に使
用されるシーラント、食品サンプルなどに使用される意
匠性が要求される材料等として有用である。
Applications The room-temperature-curable organopolysiloxane composition of the present invention is required to have design properties used for, for example, sealants used in places where the appearance of building materials is important, food samples, and the like. It is useful as a material.

【0019】[0019]

【実施例】以下に、本発明の実施例を示す。各例中、部
は重量部を示し、粘度は25℃の測定値である。以下の
説明において、比較例に係る組成物の番号には*を付し
た。番号に*が付されていない組成物は本発明の実施例
である。
Examples of the present invention will be described below. In each example, “parts” indicates “parts by weight”, and the viscosity is a measured value at 25 ° C. In the following description, * was added to the number of the composition according to the comparative example. Compositions without an asterisk (*) are examples of the present invention.

【0020】実施例1 分子鎖両未端が水酸基で停止されたジメチルポリシロキ
サン(粘度:20,000cSt)100部、煙霧質シ
リカの表面をヘキサメチルジシラザンで疎水化処理した
疎水性シリカ13部、及び二酸化チタン1.5部を混合
した。得られた混合物を三本ロールミルに1回通した
後、さらに該混合物にメチルトリブタノキシムシラン7
部、繊維長0.3mmのポリエチレン繊維5重量部及び
ジブチルスズジオクトエート0.1部を無水の状態で脱
泡、混合して、組成物1を調製した。
Example 1 100 parts of dimethylpolysiloxane (viscosity: 20,000 cSt) in which both ends of a molecular chain are terminated with a hydroxyl group, and 13 parts of hydrophobic silica obtained by hydrophobizing the surface of fumed silica with hexamethyldisilazane , And 1.5 parts of titanium dioxide. After passing the obtained mixture through a three-roll mill once, the mixture was further added with methyltributanoxime silane 7
, 5 parts by weight of polyethylene fiber having a fiber length of 0.3 mm and 0.1 part of dibutyltin dioctoate were defoamed and mixed in an anhydrous state to prepare composition 1.

【0021】実施例2 分子鎖両末端が水酸基で停止されたジメチルポリシロキ
サン(粘度:20,000cSt)100部に表面をス
テアリン酸石鹸で処理したコロイダル炭酸カルシウム6
0部、及び二酸化チタン1.5部を混合した。得られた
混合物を三本ロールミルに1回通した後、さらに該混合
物にメチルトリブタノキシムシラン7部、繊維長0.1
mmのポリエステル繊維10重量部及びジブチルスズジ
オクトエート0.1部を無水の状態で脱泡、混合して、
組成物2を調製した。
Example 2 Colloidal calcium carbonate 6 whose surface was treated with a stearic acid soap on 100 parts of dimethylpolysiloxane (viscosity: 20,000 cSt) in which both ends of a molecular chain were terminated with a hydroxyl group
0 parts and 1.5 parts of titanium dioxide were mixed. After passing the obtained mixture through a three-roll mill once, 7 parts of methyltributanoxime silane and a fiber length of 0.1 were further added to the mixture.
10 parts by weight of polyester fiber of 0.1 mm and 0.1 part of dibutyltin dioctoate are defoamed and mixed in an anhydrous state,
Composition 2 was prepared.

【0022】比較例1 ポリエチレン繊維を配合しなかった以外は実施例1と同
様にして、組成物3*を調製した。
Comparative Example 1 A composition 3 * was prepared in the same manner as in Example 1 except that polyethylene fiber was not blended.

【0023】比較例2 ポリエステル繊維を配合しなかった以外は実施例2と同
様にして、組成物4*を調製した。組成物1〜4* を厚
さ2mmのシートに成形し、得られたシートを温度20
℃、相対湿度55%の雰囲気下で7日間放置したとこ
ろ、これらのシートはいずれも硬化してゴム弾性体とな
った。得られたゴム弾性体の表面を観察し、該表面が艶
消しとなっているかどうかを観察した。また、該ゴム弾
性体の物性は、JISK 6301に準じて測定した
(硬度の測定には、スプリング式硬さ試験機A型を用い
た)。結果を表1に示す。
Comparative Example 2 A composition 4 * was prepared in the same manner as in Example 2 except that no polyester fiber was blended. The compositions 1-4 * were formed into a sheet having a thickness of 2 mm, and the obtained sheet was heated at a temperature of 20
When left in an atmosphere at a temperature of 55 ° C. and a relative humidity of 55% for 7 days, all of these sheets were cured to become rubber elastic bodies. The surface of the obtained rubber elastic body was observed, and whether or not the surface was matte was observed. The physical properties of the rubber elastic body were measured in accordance with JIS K6301 (the hardness was measured using a spring-type hardness tester type A). Table 1 shows the results.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【発明の効果】本発明の室温硬化性オルガノポリシロキ
サン組成物は、比重が特に大きくなく、良好な機械的物
性を有しながら表面が艶消しである硬化物を与える。
The room-temperature-curable organopolysiloxane composition of the present invention has a specific gravity which is not particularly high, and gives a cured product having good mechanical properties and a matte surface.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C08G 83/06 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int.Cl. 7 , DB name) C08G 83/06

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 (a) 分子鎖両末端が水酸基で停止されたジオルガノポリシロ キサン 100重量部、 (b) 一分子中にけい素原子に結合した加水分解性基を少なくとも3個有する有 機けい素化合物及びその部分加水分解物からなる群より選ばれる少なくとも一種 0.5〜30重量部、 (c) 無機充填剤 1〜500重量部、 及び (d) 繊維長が0.01〜0.5mmである繊維状樹脂 0.1〜20重量部 を含有してなる、水を含有せず、吸湿することにより硬
化し得る室温硬化性オルガノポリシロキサン組成物。
(1) 100 parts by weight of a diorganopolysiloxane having both ends of a molecular chain terminated by a hydroxyl group, and (b) a compound having at least three hydrolyzable groups bonded to a silicon atom in one molecule. At least one selected from the group consisting of a silicon compound and a partial hydrolyzate thereof, 0.5 to 30 parts by weight, (c) 1 to 500 parts by weight of an inorganic filler, and (d) a fiber length of 0.01 to 0. 0.1 to 20 parts by weight of a fibrous resin having a diameter of 0.5 mm, containing no water and hardening by absorbing moisture.
A room temperature curable organopolysiloxane composition which can be converted into a composition.
JP5351844A 1993-12-27 1993-12-27 Room temperature curable organopolysiloxane composition Expired - Fee Related JP3022124B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5351844A JP3022124B2 (en) 1993-12-27 1993-12-27 Room temperature curable organopolysiloxane composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5351844A JP3022124B2 (en) 1993-12-27 1993-12-27 Room temperature curable organopolysiloxane composition

Publications (2)

Publication Number Publication Date
JPH07188560A JPH07188560A (en) 1995-07-25
JP3022124B2 true JP3022124B2 (en) 2000-03-15

Family

ID=18419995

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5351844A Expired - Fee Related JP3022124B2 (en) 1993-12-27 1993-12-27 Room temperature curable organopolysiloxane composition

Country Status (1)

Country Link
JP (1) JP3022124B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4395270B2 (en) * 2001-05-11 2010-01-06 信越化学工業株式会社 Room temperature fast-curing olga polysiloxane composition
JP2003020413A (en) * 2001-07-10 2003-01-24 Cemedine Co Ltd Highly designable composition
FR2857016B1 (en) * 2003-07-03 2007-08-31 Rhodia Performances Fibres MINERAL LOADS FOR IMPROVING THE MATERIAL OF THERMOPLASTIC POLYMERS
JP4744972B2 (en) * 2005-08-01 2011-08-10 モメンティブ・パフォーマンス・マテリアルズ・ジャパン合同会社 Curable polyorganosiloxane composition for building
JP4821986B2 (en) 2006-06-07 2011-11-24 信越化学工業株式会社 Potting material or coating material comprising matte liquid organopolysiloxane composition, matte cured product, and surface gloss reduction method

Also Published As

Publication number Publication date
JPH07188560A (en) 1995-07-25

Similar Documents

Publication Publication Date Title
JPS601898B2 (en) Organosiloxane composition that cures to provide an elastomer
WO2016117206A1 (en) Room temperature-curable organopolysiloxane composition
JPS62127348A (en) Room-temperature curing silicone rubber composition
JP3517479B2 (en) Method for producing one-part room temperature curable silicone elastomer composition
JP2000129130A (en) Production of room temperature-curable organopolysiloxane composition
JPS61225250A (en) Room temperature curing organosiloxane composition
JP2841155B2 (en) Room temperature curable organopolysiloxane composition
JP2004182942A (en) Room temperature curable organopolysiloxane composition
JP3022124B2 (en) Room temperature curable organopolysiloxane composition
JPH05140454A (en) Room temperature-curing organopolysiloxane composition
US4477606A (en) Water resistant room temperature vulcanizable polyorganosiloxane compositions and method for preparing same
JP3457075B2 (en) Method for producing one-part room temperature curable silicone elastomer composition
JP5545924B2 (en) Room temperature curable polyorganosiloxane composition
JPH09227780A (en) Room temperature curing organopolysiloxane composition
JP2816930B2 (en) Room temperature curable organopolysiloxane composition
JP2574080B2 (en) Room temperature curable organopolysiloxane composition and cured product thereof
JPH0616940A (en) Room temperature curing organopolysiloxane composition and its cured material
JP4183940B2 (en) Room temperature curable polyorganosiloxane composition
JPH0211659A (en) Sealing composition
JPH08104815A (en) One pack type room temperature curable silicone elastomer compositon
JP2582685B2 (en) Method for producing room temperature curable organopolysiloxane composition
JPH07133430A (en) Room temperature curable polyorganosiloxane composition
JPH05263063A (en) Adhesive for gasket
JPH08208991A (en) Method for producing room temperature curable polyorganosiloxane composition having improved dripping property
JPS6018545A (en) Adhesive polyorganosiloxane composition

Legal Events

Date Code Title Description
FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090114

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100114

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110114

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110114

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120114

Year of fee payment: 12

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130114

Year of fee payment: 13

LAPS Cancellation because of no payment of annual fees