JPH0826300B2 - Sealant contamination prevention method - Google Patents

Sealant contamination prevention method

Info

Publication number
JPH0826300B2
JPH0826300B2 JP2404288A JP2404288A JPH0826300B2 JP H0826300 B2 JPH0826300 B2 JP H0826300B2 JP 2404288 A JP2404288 A JP 2404288A JP 2404288 A JP2404288 A JP 2404288A JP H0826300 B2 JPH0826300 B2 JP H0826300B2
Authority
JP
Japan
Prior art keywords
sealing material
polyurethane
component
prepolymer
isocyanate
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 - Lifetime
Application number
JP2404288A
Other languages
Japanese (ja)
Other versions
JPH01201386A (en
Inventor
紀英 高木
正伸 相原
俊宏 高野
善明 高仲
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.)
OOTO KAGAKU KOGYO KK
Original Assignee
OOTO KAGAKU KOGYO KK
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 OOTO KAGAKU KOGYO KK filed Critical OOTO KAGAKU KOGYO KK
Priority to JP2404288A priority Critical patent/JPH0826300B2/en
Publication of JPH01201386A publication Critical patent/JPH01201386A/en
Publication of JPH0826300B2 publication Critical patent/JPH0826300B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Sealing Material Composition (AREA)
  • Paints Or Removers (AREA)

Description

【発明の詳細な説明】 本発明はシーリング材の硬化時、目地等の表面の粘着
性の改良に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvement of tackiness of a surface such as a joint during curing of a sealing material.

詳細には、本発明においては、ポリイソシアネートポ
リウレタンプレポリマーの溶液を、施工後の未硬化状態
のシーリング材の表面に付与する事によって、シーリン
グ材表面部の硬化を早めると共に表面粘着性を改良する
ことによって、シーリング材表面への塵埃等の付着を防
止する事が出来、シーリング材の汚染防止を可能とし
た。一般に一液型及び二液型の、変成シリコーンやポリ
ウレタンシーリング材は硬化時、その表面に粘着性が数
日乃至数ケ月間残る(今後“アフタータック”と称す
る)。変成シリコーンについてはJIS A5758に定義され
ている。
Specifically, in the present invention, a solution of the polyisocyanate polyurethane prepolymer is applied to the surface of the uncured sealing material after application to accelerate the curing of the sealing material surface portion and improve the surface tackiness. By doing so, it is possible to prevent dust and the like from adhering to the surface of the sealing material, and to prevent contamination of the sealing material. In general, one-component and two-component modified silicone and polyurethane sealing materials, when cured, remain tacky on their surfaces for days or months (hereinafter referred to as "after-tack"). Modified silicone is defined in JIS A5758.

このために、例えば建築物の目地にシーリング材を施
工した時、アフタータック期間中にゴミや土埃り等が目
地表面に付着汚染し美観を害ねる問題があり、改良が強
く要望されている。
For this reason, for example, when a sealing material is applied to joints of a building, there is a problem that dust and dirt adhere to the joint surface and contaminate the joint surface during aftertack, and improvement is strongly desired.

アフタータック改良の試みは以前よりいろいろ検討さ
れている。例えばシーリング基材中の無機フライー類を
増量するとか、揺変付与剤であるコロイダルシリカやポ
リウレア粉末等を増量して使用する事、又は樹脂成分中
のイソシアネート基やシリケート基等の官能基濃度を増
して架橋密度を高める手段等によって或程度の改良は出
来る。しかしながら、これらの手段では液の粘度が高く
なり作業性が劣ったり、又硬化後のシーリング材の硬度
が高くなり、破断伸長率の減少やモジュラスのアップを
起こし、シーリング材の重要性能である伸縮追随性を悪
化させるなどの欠点があり実用的ではない。
Various attempts have been made to improve after-tack. For example, by increasing the amount of inorganic flies in the sealing base material, or by increasing the amount of thixotropic agent colloidal silica or polyurea powder, or by using functional groups such as isocyanate groups and silicate groups in the resin component. A certain degree of improvement can be made by means of increasing the crosslinking density. However, with these means, the viscosity of the liquid is high and the workability is poor, and the hardness of the sealing material after curing is high, which causes a decrease in elongation at break and an increase in modulus, which is an important performance of the sealing material. It is not practical because it has drawbacks such as poor followability.

本発明の方法においては、目地等の空隙に充填したポ
リウレタンや変成シリコーン等のシーリング材に、その
完全硬化前好ましくは充填直後にその表面に、分子末端
にイソシアネート基を2個以上含むポリウレタンプレポ
リマーの不活性有機溶剤溶液を、スプレー又は刷毛等に
より付与する。本方法によりシーリング材表面の硬化を
早め且つ表面粘着性を除去する事が出来るので、シーリ
ング材の汚染を防止する事が出来た。
In the method of the present invention, a polyurethane prepolymer containing two or more isocyanate groups at the molecular end of a sealing material such as polyurethane or modified silicone filled in voids such as joints is preferably on the surface of the sealing material before complete curing, preferably immediately after filling. The inert organic solvent solution of is applied by spraying or brush. By this method, it is possible to accelerate the curing of the surface of the sealing material and remove the surface tackiness, so that it is possible to prevent the sealing material from being contaminated.

使用されるポリウレタンシーリング材としては、例え
ば過剰量のTD1、MD1などのポリイソシアネートと、ポリ
エーテルポリオール等のポリオール類との反応により得
られるイソシアネート基末端ポリウレタンプレポリマー
と、フライー類等を含有し、使用時空気中の湿気により
硬化する一液型ポリウレタンシーリング材がある。
The polyurethane sealing material used, for example, an excess amount of polyisocyanate such as TD1, MD1 and the like, an isocyanate group-terminated polyurethane prepolymer obtained by the reaction of polyols such as polyether polyol, and the like, and containing flies, There is a one-component polyurethane sealing material that cures due to moisture in the air during use.

又前記の様なイソシアネート基末端ウレタンプレポリ
マーを主成分とする主剤と、ポリオール類とフライー類
等とを含有する硬化剤とを使用時に混合して反応硬化さ
せる、二液型のポリウレタンシーリング材も用いられ
る。このほか、分子末端にアルコキシシラン基を有する
変成シリコーン系シーリング材にも一液型と二液型が市
販されてある。
In addition, a two-component polyurethane sealing material in which a main agent containing an isocyanate group-terminated urethane prepolymer as a main component as described above and a curing agent containing a polyol and a fly, etc., are mixed and reacted and cured at the time of use Used. In addition, one-part type and two-part type are also commercially available as modified silicone-based sealing materials having an alkoxysilane group at the molecular end.

本発明の汚染防止方法は一般シーリング材に適用可能
であるが、一液型又は二液型変成シリコーンシーリング
材及び、一液型又は二液型のポリウレタンシーリング材
に特に有効である。
The contamination prevention method of the present invention can be applied to general sealing materials, but is particularly effective for one-component or two-component modified silicone sealing materials and one-component or two-component polyurethane sealing materials.

本発明に使用される分子末端にイソシアネート基を含
有するポリウレタンプレポリマーについて説明する。
The polyurethane prepolymer having an isocyanate group at the molecular end used in the present invention will be described.

原料イソシアネートとしてはトルエンジイソシアネ
ート、ジフェニルメタンジイソシアネート、ポリフェニ
ルメタンポリイソシアネートなどの芳香族イソシアネー
トやヘキサメチレンジイソシアネート、イソホロンジ
イソシアネート、キシレンジイソシアネート、核水添キ
シレンジイソシアネートなどの脂肪族系等のイソシアネ
ート類があげられるが、後者のイソシアネート類を原料
とした場合には得られた塗膜の耐候性、耐変色性、目地
周辺への非汚染性等が良好であり特に好ましい。
Examples of the raw material isocyanate include toluene diisocyanate, diphenylmethane diisocyanate, aromatic isocyanate such as polyphenylmethane polyisocyanate and hexamethylene diisocyanate, isophorone diisocyanate, xylene diisocyanate, and aliphatic isocyanate such as nuclear hydrogenated xylene diisocyanate. When the latter isocyanate is used as a raw material, the resulting coating film has good weather resistance, discoloration resistance, non-staining property around the joint, and the like, and is particularly preferable.

前記ポリイソシアネート類と組み合わせるポリオール
成分としては、ポリオキシプロピレンポリオール、ポリ
エステルポリオール、ポリアクリルポリオール、やエチ
レングリコールなどの単分子ポリオールなど一般ポリウ
レタン樹脂に使用されるポリオール類が使用出来る。
As the polyol component to be combined with the polyisocyanate, polyols used for general polyurethane resins such as polyoxypropylene polyol, polyester polyol, polyacrylic polyol, and monomolecular polyol such as ethylene glycol can be used.

溶剤類としては酢酸エチル、メチルエチルケトン、ト
ルエン、キシレン、ヘキサン、ジメチルエーテルなど活
性水素化合物を含有しない不活性溶剤が用いられる。
As the solvent, an inert solvent containing no active hydrogen compound such as ethyl acetate, methyl ethyl ketone, toluene, xylene, hexane or dimethyl ether is used.

本発明ではまた必要に応じて可塑剤、フイラー、顔料
艶消剤、増粘剤、安定剤、触媒などの添加剤を配合する
ことも出来る。
In the present invention, additives such as a plasticizer, a filler, a pigment matting agent, a thickener, a stabilizer, and a catalyst can be blended, if necessary.

本発明に使用するポリイソシアネートウレタンプレポ
リマーの作用の役割については不明な点があるが、例え
ば1液ポリウレタンシーラントについては未硬化のシー
リング材表面に塗布した場合、プレポリマーの一部はシ
ーリング材表層部に浸透するとともに、イソシアネート
基が比較的速やかに空気中の水分と反応を起こして表層
部にポリウレタン、ポリウレアの高架橋密度の樹脂を作
り密着固化してシーリング材表面の硬化を早めアフター
タックを防止する。他方、比較的分子量が高く弾性のあ
る皮膜を作るポリイソシアネートプレポリマーはシーリ
ング材表面への親和性が良く、均一の可撓性ある皮膜を
表面に作る事によって、長期的汚染防止と耐候性向上に
有効であると考えられる。
Although the role of the action of the polyisocyanate urethane prepolymer used in the present invention is unclear, for example, in the case of a one-component polyurethane sealant, when it is applied to the surface of an uncured sealant, a part of the prepolymer is a surface layer of the sealant. As it penetrates into the surface, the isocyanate groups react relatively quickly with the water in the air to form a highly cross-linked resin of polyurethane and polyurea on the surface, which solidifies and solidifies to accelerate the curing of the sealing material surface and prevent after-tack. To do. On the other hand, polyisocyanate prepolymer, which forms a film with a relatively high molecular weight and elasticity, has a good affinity for the surface of the sealing material, and by forming a uniform and flexible film on the surface, prevention of long-term contamination and improvement of weather resistance Considered to be effective.

ポリウレタンプレポリマーが低分子のみから成る場合
には、塗膜は硬く弾性がない為に、シーリング材の伸縮
に追従出来ず亀裂を生じて好ましく無い。
When the polyurethane prepolymer is composed only of low molecular weight, the coating film is hard and has no elasticity, so that it cannot follow the expansion and contraction of the sealing material and cracks are generated, which is not preferable.

本イソシアネートプレポリマーをシーリング材表面に
塗装した場合、シーリング材の内部深くまで浸透する事
はないので、シーリング材のモジュラス、伸縮性を悪化
する事が無く、従って、元のシーリング材の保有する諸
物性に悪影響を与えない。
When this isocyanate prepolymer is coated on the surface of the sealing material, it does not penetrate deep into the inside of the sealing material, so the modulus and elasticity of the sealing material are not deteriorated. Does not adversely affect the physical properties.

本発明の施工例としては、目地部に前記一液型又は二
液型のシーリング材を充填し、ヘラ押え仕上げ後目地周
辺のマスキングテープを除去する前または後に、前記ポ
リイソシアネートウレタンプレポリマーの溶液を、刷
毛、エヤスプレー、エヤレススプレー、エヤゾール型ス
プレー等により目地表面に均一に薄くコーテングする。
As a construction example of the present invention, a joint part is filled with the one-component or two-component type sealing material, and before or after removing the masking tape around the joint after the spatula-holding finish, a solution of the polyisocyanate urethane prepolymer. With a brush, an air spray, an airless spray, an aerosol spray, or the like to coat the joint surface evenly and thinly.

本汚染防止方法を行う事により、無処理の場合に比
し、シーリング材の表面の硬化が早く、アフタータック
期間が大巾に短縮出来るので、非汚染性で耐候性の改良
されたシーリング材が得られた。
By carrying out this pollution prevention method, the surface of the sealing material is hardened faster and the after-tack period can be greatly shortened compared to the case without treatment, so a sealing material with non-contamination and improved weather resistance can be obtained. Was obtained.

次に実施例によって本発明を説明するが、本発明はこ
れに限定されるものではない。
Next, the present invention will be described with reference to examples, but the present invention is not limited thereto.

〔合成例−1〕 窒素ガスで置換した1Lの4ッ口フラスコに、グリセリ
ンにプロピレンオキサイドを付加した分子量400のポリ
エーテルトリオール33.6(g)、イソホロンジイソシア
ネート55.9(g)、ジブチル錫ジラウレート0.45
(g)、脱水酢酸エチル810.0(g)を仕込み、75℃で
3時間の反応を行い、イソシアネート濃度1.12(%)の
ウレタンプレポリマー溶液〔A〕を得た。
[Synthesis Example-1] In a 1 L four-necked flask substituted with nitrogen gas, polyethertriol having a molecular weight of 400 in which propylene oxide was added to glycerin 33.6 (g), isophorone diisocyanate 55.9 (g), dibutyltin dilaurate 0.45
(G) and 810.0 (g) of dehydrated ethyl acetate were charged and reacted at 75 ° C. for 3 hours to obtain a urethane prepolymer solution [A] having an isocyanate concentration of 1.12 (%).

〔合成例−2〕 窒素ガスで置換した1Lの4ッ口フラスコに、トリメチ
ロールプロパンにε−カプロラクトンを付加した分子量
500のポリカプロラクトントリオール34.8(g)、水素
添加MD1 54.7(g)、オクチル酸第一錫0.45(g)、脱
水酢酸エチル810.0(g)を仕込み、75℃で3時間の反
応を行い、イソシアネート濃度0.93(%)のウレタンプ
レポリマー溶液〔B〕を得た。
[Synthesis Example-2] Molecular weight obtained by adding ε-caprolactone to trimethylolpropane in a 1 L 4-neck flask substituted with nitrogen gas.
500 polycaprolactone triol 34.8 (g), hydrogenated MD1 54.7 (g), stannous octylate 0.45 (g), dehydrated ethyl acetate 810.0 (g) were charged and reacted at 75 ° C for 3 hours to obtain isocyanate concentration. A urethane prepolymer solution [B] of 0.93 (%) was obtained.

〔合成例−3〕 窒素ガスで置換した1Lの4ッ口フラスコに、エチレン
グリコールにε−カプロラクトンを付加した分子量500
のポリカプロラクトンジオール17.6(g)、トリメチロ
ールプロパン9.4(g)、イソホロンジイソシアネート6
2.5(g)、ジブチル錫ジラウレート0.45(g)、脱水
酢酸エチル810.0(g)を仕込み、75℃で3時間の反応
を行い、イソシアネート濃度1.25(%)のウレタンプレ
ポリマー溶液〔C〕を得た。
[Synthesis Example-3] In a 1 L 4-necked flask substituted with nitrogen gas, a molecular weight of 500 obtained by adding ε-caprolactone to ethylene glycol was added.
Polycaprolactone diol 17.6 (g), trimethylolpropane 9.4 (g), isophorone diisocyanate 6
2.5 (g), dibutyltin dilaurate 0.45 (g) and dehydrated ethyl acetate 810.0 (g) were charged and reacted at 75 ° C. for 3 hours to obtain a urethane prepolymer solution [C] having an isocyanate concentration of 1.25 (%). .

〔実施例−1〕 市販の1成分形ポリウレタンシーリング材および1成
分形低モジュラス変成シリコーンシーリング材を目地に
充填し、直ちに先に合成したプレポリマー溶液〔A〕、
〔B〕を市販の噴霧器で均一に吹付けた。これら試料に
ついて、20℃60%RHにおけるタックフリー(指触乾燥時
間)、3日後のアフタータック(硬化後の粘着性)なら
びに屋外に3ケ月間暴露したときの汚染の状況を評価し
た。その結果を表−1に示す。
[Example-1] A commercially available one-component type polyurethane sealing material and a one-component type low modulus modified silicone sealing material were filled in the joints, and immediately the prepolymer solution [A] synthesized previously was prepared.
[B] was uniformly sprayed with a commercially available atomizer. These samples were evaluated for tack-free at 20 ° C. and 60% RH (drying time to the touch), after-tack after 3 days (adhesiveness after curing), and contamination status when exposed outdoors for 3 months. The results are shown in Table-1.

〔比較例−1〕 実施例−1で使用したシーリング材を目地に充填し、
そのまま硬化させた。これら試料について実施例−1と
同様の試験を行い評価した。その結果を表−1に示す。
[Comparative Example-1] Filling the joint with the sealing material used in Example-1,
It was allowed to cure. These samples were evaluated by conducting the same tests as in Example-1. The results are shown in Table-1.

〔実施例−2〕 市販の2成分形低モジュラスポリウレタンシーリング
材および2成分形変成シリコーンシーリング材を目地に
充填し、直ちに先に合成したプレポリマー溶液〔A〕、
〔C〕を市販の噴霧器で均一に吹付けた。これら試料に
ついて、実施例−1と同様の試験を行い評価した。その
結果を表−2に示す。
[Example-2] A commercially available two-component low-modulus polyurethane sealing material and a two-component modified silicone sealing material were filled in the joints, and immediately the prepolymer solution [A] synthesized previously was used.
[C] was uniformly sprayed with a commercially available atomizer. These samples were evaluated by conducting the same tests as in Example-1. The results are shown in Table-2.

〔比較例−2〕 実施例−2で使用したシーリング材を目地に充填し、
そのまま硬化させた。これら試料について実施例−1と
同様の試験を行い評価した。その結果を表−2に示す。
[Comparative Example-2] The joint was filled with the sealing material used in Example-2,
It was allowed to cure. These samples were evaluated by conducting the same tests as in Example-1. The results are shown in Table-2.

上の結果から明らかなように、ウレタンプレポリマー
溶液の吹付けは、タックフリーの短縮、アフタータック
の改善に非常に優れた効果を示す。したがって、タイル
目地やサイディング目地等、暴露される箇所にシーリン
グ材を使用する場合、この工法は汚染の防止に対し極め
て有効な方法となる。
As is clear from the above results, the spraying of the urethane prepolymer solution shows a very excellent effect in shortening tack-free and improving after-tack. Therefore, when a sealing material is used in exposed areas such as tile joints and siding joints, this method is extremely effective for preventing contamination.

〔注:表−1及び表−2において、 一成分形ポリウレタンシーリング材はオート化学工業
(株)製のオートン101Aであり; 一成分形変成シリコーンシーリング材はセメダイン工
業(株)製のポスシールLMであり;二成分形ポリウレタ
ンシーリング材は保土谷建材(株)製のミリオネートNS
であり;二成分形シリコーンシーリング材は横浜ゴム
(株)製のハマタイトスーパーIIである。〕
[Note: In Tables 1 and 2, the one-component polyurethane sealing material is Auton 101A manufactured by Auto Chemical Co., Ltd .; the one-component modified silicone sealing material is Posseal LM manufactured by Cemedine Industry Co., Ltd. Yes; the two-component polyurethane sealing material is Millionate NS manufactured by Hodogaya Kenzai Co., Ltd.
The two-component silicone sealing material is Hamatite Super II manufactured by Yokohama Rubber Co., Ltd. ]

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】未硬化状態のシーリング材表面に、ポリイ
ソシアネートウレタンプレポリマーの溶液を付与する事
を特徴とする、シーリング材の汚染防止方法。
1. A method for preventing contamination of a sealing material, which comprises applying a solution of a polyisocyanate urethane prepolymer to the surface of the uncured sealing material.
【請求項2】シーリング材がポリウレタン系または変性
シリコーン系である、請求項1記載のシーリング材の汚
染防止方法。
2. The method for preventing contamination of a sealing material according to claim 1, wherein the sealing material is a polyurethane type or a modified silicone type.
【請求項3】前記プレポリマーが、脂肪族系または芳香
脂肪族系または脂環族系の分子末端イソシアネート基を
2個以上含有するポリウレタンプレポリマーの、有機溶
剤溶液である事を特徴とする、請求項1記載のシーリン
グ材の汚染防止方法。
3. The prepolymer is a solution of a polyurethane prepolymer containing two or more aliphatic, araliphatic, or alicyclic molecular terminal isocyanate groups in an organic solvent. The method for preventing contamination of the sealing material according to claim 1.
JP2404288A 1988-02-05 1988-02-05 Sealant contamination prevention method Expired - Lifetime JPH0826300B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2404288A JPH0826300B2 (en) 1988-02-05 1988-02-05 Sealant contamination prevention method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2404288A JPH0826300B2 (en) 1988-02-05 1988-02-05 Sealant contamination prevention method

Publications (2)

Publication Number Publication Date
JPH01201386A JPH01201386A (en) 1989-08-14
JPH0826300B2 true JPH0826300B2 (en) 1996-03-13

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JP2404288A Expired - Lifetime JPH0826300B2 (en) 1988-02-05 1988-02-05 Sealant contamination prevention method

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Cited By (1)

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Publication number Priority date Publication date Assignee Title
JP2006326546A (en) * 2005-05-30 2006-12-07 Pialex Technologies Corp Coating film and coating film forming method

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0384087A (en) * 1989-08-28 1991-04-09 Hitachi Kasei Polymer Kk Retardant for two-component modified silicone-based sealing material
JP5515393B2 (en) * 2009-04-30 2014-06-11 横浜ゴム株式会社 Topcoat composition for polysulfide sealant
JP2013167154A (en) * 2013-06-06 2013-08-29 Sekisui Fuller Co Ltd Repair method for exterior wall
JP6709357B2 (en) * 2015-08-11 2020-06-17 オート化学工業株式会社 Surface coating agent and method using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006326546A (en) * 2005-05-30 2006-12-07 Pialex Technologies Corp Coating film and coating film forming method

Also Published As

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