JP2790929B2 - Repair method of building wall - Google Patents

Repair method of building wall

Info

Publication number
JP2790929B2
JP2790929B2 JP27547891A JP27547891A JP2790929B2 JP 2790929 B2 JP2790929 B2 JP 2790929B2 JP 27547891 A JP27547891 A JP 27547891A JP 27547891 A JP27547891 A JP 27547891A JP 2790929 B2 JP2790929 B2 JP 2790929B2
Authority
JP
Japan
Prior art keywords
coating
silicone
repair method
group
cleaning agent
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
JP27547891A
Other languages
Japanese (ja)
Other versions
JPH05113041A (en
Inventor
好昭 竹澤
久雄 茂木
昭浩 星野
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.)
Momentive Performance Materials Japan LLC
Original Assignee
Toshiba Silicone 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
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Application filed by Toshiba Silicone Co Ltd filed Critical Toshiba Silicone Co Ltd
Priority to JP27547891A priority Critical patent/JP2790929B2/en
Publication of JPH05113041A publication Critical patent/JPH05113041A/en
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の技術分野】本発明は、建築物壁面の補修方法に
関し、さらに詳しくは建築物の外装壁面にコーティング
剤を塗布することにより、壁面表面の耐磨耗性、耐候
性、美観の向上などを付与することができ、さらに洗浄
剤による除去が可能なため補修が容易な建築物壁面の保
護方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for repairing a building wall, and more particularly, to improving the abrasion resistance, weather resistance and aesthetic appearance of a wall surface by applying a coating agent to an exterior wall of the building. The present invention relates to a method for protecting a building wall surface, which can be easily repaired because it can be removed by a cleaning agent.

【0002】[0002]

【発明の技術的背景とその問題点】建築物の壁面は排気
ガス、酸性雨、砂塵などの影響や、塩害、凍害などを受
けて表面が劣化し、美観が低下するという問題がある。
そのため、建築物壁面の美観の低下を防止する方法、お
よび美観の低下した壁面を補修する方法が種々検討され
ている。補修する方法としては、例えば洗浄剤を用いて
壁面の表面を洗浄し汚れを除去する方法がある。しかし
ながら洗浄剤を用いての方法は、壁面表面に付着した汚
れを除去できても、洗浄剤およびブラシ等の影響を受け
るため、表面の美観を再度向上させるまでには至らな
い。洗浄後の美観向上剤として、炭化水素などのワック
ス成分を主成分とした水性エマルジョン溶液や有機溶剤
溶液を塗布することも提案されているが、埃の巻き込み
による汚れの再付着、耐水性不良に伴う被膜の流れ落ち
や剥離等の問題があった。また石膏を主成分とするコー
ティング剤なども提案されているが、硬化時の収縮によ
る被膜表面のクラック、反り等の発生の問題があった。
また、コンクリートなどの多孔質無機材料などに、シラ
ン化合物やポリシロキサンを主成分とするコーティング
剤を塗布し、撥水性を付与して劣化を防止する方法が知
られている(特開昭57−126878号公報、特開昭
62−197369号公報、特開平1−292089号
公報、特開平2−70787号公報、特開平2−150
477号公報参照)。しかし、美観の低下した壁面の補
修方法や、コーティング剤を塗布後の再補修方法につい
ては記載されておらず、さらに改善が必要であった。
Technical Background of the Invention and Problems There is a problem that the wall surface of a building is deteriorated due to the influence of exhaust gas, acid rain, dust and the like, salt damage, frost damage, etc., and the appearance is deteriorated.
Therefore, various methods for preventing the deterioration of the aesthetic appearance of the building wall surface and for repairing the wall surface having the reduced aesthetic appearance have been studied. As a method of repairing, for example, there is a method of cleaning the surface of a wall surface with a cleaning agent to remove dirt. However, in the method using a cleaning agent, even if dirt adhering to the wall surface can be removed, the surface appearance is not improved again because of the influence of the cleaning agent and the brush. As an aesthetic improver after washing, it has been proposed to apply an aqueous emulsion solution or an organic solvent solution containing a wax component such as a hydrocarbon as a main component. There have been problems such as falling of the coating and peeling. Although a coating agent containing gypsum as a main component has been proposed, there has been a problem in that cracks and warpage of the coating surface occur due to shrinkage during curing.
In addition, a method is known in which a coating agent containing a silane compound or polysiloxane as a main component is applied to a porous inorganic material such as concrete to impart water repellency to prevent deterioration (Japanese Patent Application Laid-Open No. 57-157). 126878, JP-A-62-197369, JP-A-1-292889, JP-A-2-70787, JP-A-2-150
No. 477). However, there is no description on a method for repairing the wall surface with a reduced appearance and a method for repairing the wall surface after applying the coating agent, and further improvement is required.

【0003】[0003]

【発明の目的】本発明は、上記の問題点を解消し、排気
ガス、酸性雨、砂塵等の影響や塩害、凍害等による建築
物壁面の劣化に対し、優れた耐磨耗性、耐候性、美観の
向上等を付与することができ、しかも再度の補修の容易
な建築物壁面の補修方法を提供することを目的とする。
An object of the present invention is to solve the above-mentioned problems and to provide excellent abrasion resistance and weather resistance against the effects of exhaust gas, acid rain, dust and the like, and the deterioration of the building wall surface due to salt damage and frost damage. It is an object of the present invention to provide a method for repairing a building wall surface which can provide an improvement in aesthetic appearance and the like and which can be easily repaired again.

【0004】[0004]

【発明の構成】本発明者らは、上記目的を達成するため
に種々検討した結果、建築物の壁面に洗浄剤で除去可能
な、シリコーンを主成分とする保護被膜を設けることに
より、優れた耐磨耗性、耐候性、美観の向上等を付与す
ることができ、再度の補修も容易な建築物壁面の補修方
法を提供できることを見出し、本発明を成すに至った。
すなわち、本発明の建築物壁面の補修方法は、建築物の
壁面に洗浄剤で除去可能な、シリコーンを主成分とする
コーティング剤を塗布することを特徴とする。
The present inventors have conducted various studies in order to achieve the above object, and as a result, by providing a protective coating containing silicone as a main component, which can be removed with a cleaning agent, on the wall of a building, excellent results have been obtained. The present inventors have found that it is possible to provide a method for repairing a building wall surface, which can improve wear resistance, weather resistance, aesthetic appearance, and the like, and that can easily be repaired again, and have accomplished the present invention.
That is, the method for repairing a building wall according to the present invention is characterized in that a coating agent containing silicone as a main component that can be removed with a cleaning agent is applied to the wall of the building.

【0005】本発明の方法においては、対象とされる建
築物の壁面の材質は、通常使用されているものであれば
特に限定されない。壁面の材質としてはコンクリート、
モルタル、タイル、レンガ、石材などの無機質材料、ア
ルミニウム、鉄、ステンレスなどの金属材料など、およ
びそれらの表面を合成樹脂吹付材、ケイ酸質吹付材など
で吹付処理したもの、またさらに合成樹脂塗料などで塗
装処理したものなどが例示される。ここで合成樹脂吹付
材や合成樹脂塗料としてはウレタン樹脂系、アクリル樹
脂系、エポキシ樹脂系などが、ケイ酸質吹付材としては
シリカゾール系、水ガラス系、ケイ酸塩材料系などが例
示される。本発明の補修方法が特に光沢の付与などによ
る美観の向上に効果があることから、上記の中でも光沢
を有するような非多孔性の壁面に対して特に好ましく使
用される。また再補修時の洗浄剤による除去が容易であ
ることからも、コーティング剤の浸透の少ない非多孔性
の壁面に対して好ましく使用される。
[0005] In the method of the present invention, the material of the wall surface of the target building is not particularly limited as long as it is a commonly used material. Concrete wall materials
Inorganic materials such as mortar, tile, brick, stone, etc., metal materials such as aluminum, iron, stainless steel, etc., and their surfaces sprayed with synthetic resin spraying material, siliceous spraying material, etc., and further synthetic resin paint And the like. Here, urethane resin type, acrylic resin type, epoxy resin type and the like are exemplified as the synthetic resin spraying material and the synthetic resin paint, and silica sol type, water glass type and silicate material type are exemplified as the siliceous spraying material. . Since the repair method of the present invention is particularly effective in improving aesthetics by imparting gloss, it is particularly preferably used for non-porous wall surfaces having gloss among the above. In addition, it is preferably used for non-porous wall surfaces where the penetration of the coating agent is small because it is easy to remove with a cleaning agent at the time of repair.

【0006】本発明のコーティング剤はシリコーンを主
成分とし、さらに一般に溶剤、硬化触媒を含有する。本
発明で使用するシリコーンはR1Si(OH)3 で示されるオル
ガノシラントリオールまたはその部分加水分解物を主成
分として、これを縮合させることにより得られる。ここ
でR1は炭素数1〜3のアルキル基およびアリール基から
なる群より選ばれる1価の基を表し、炭素数1〜3のア
ルキル基としてはメチル基、エチル基、プロピル基が、
またアリール基としてはフェニル基などが例示される。
The coating agent of the present invention contains silicone as a main component and generally contains a solvent and a curing catalyst. The silicone used in the present invention is obtained by condensing an organosilanetriol represented by R 1 Si (OH) 3 or a partial hydrolyzate thereof as a main component. Here, R 1 represents a monovalent group selected from the group consisting of an alkyl group having 1 to 3 carbon atoms and an aryl group. Examples of the alkyl group having 1 to 3 carbon atoms include a methyl group, an ethyl group, and a propyl group.
Examples of the aryl group include a phenyl group.

【0007】オルガノシラントリオールは、対応する加
水分解性シランを加水分解することによって得られ、例
えば式R1Si(OR2)3(式中R2は炭素数1〜4のアルキル基
を表す)で示されるオルガノトリアルコキシシランを、
触媒の存在下で加水分解することにより得ることができ
る。ここでR2としては、メチル基、エチル基、プロピル
基、ブチル基などが例示される。また加水分解性基とし
て前記アルコキシ基以外のケトオキシム基、アシロキシ
基、アミノ基、アミノキシ基、アルケニルオキシ基、ア
ミド基および塩素原子などを有する加水分解性シランも
使用可能であるが、取扱いが容易なことから加水分解性
基としてアルコキシ基を有するものが好ましい。使用す
ることができる加水分解触媒としては、無水酢酸、氷酢
酸、プロピオン酸、クエン酸、安息香酸、ギ酸、シュウ
酸等の有機酸;アルミニウムアルキルアセテート等のア
ルミニウムキレート化合物;テトラクロロシラン、メチ
ルトリクロロシラン、ジメチルジクロロシラン等のクロ
ロシラン;アンモニア水等の無機アルカリ性化合物;エ
チレンジアミン等の有機アルカリ化合物;γ−アミノプ
ロピルトリメトキシシラン等のアミノ基含有有機ケイ素
化合物などが例示される。これらの中でもクロロシラン
はシリコーンの原料と加水分解触媒を兼ね、好ましく使
用される。中でもメチルトリクロロシランおよびジメチ
ルジクロロシランが好ましい。シリコーンの原料として
は、この他にR3 2SiX2 、R4 3SiX、SiX4(ここでR3、R4
前記R1と同様な置換基を示し、X は同一または相異なる
加水分解性基または水酸基を表す)で示されるシランを
使用してもよい。特に保護被膜の耐久性の優れることか
らR3 2SiX2 の使用が好ましい。この場合オルガノシラン
トリオール/R3 2SiX2 のモル比は、保護被膜の耐磨耗
性、光沢などから 0.2/0.8 以上が好ましく、また保護
被膜の洗浄剤による洗浄性から0.9/0.1 以下が好まし
い。特に好ましくは、 0.6/0.4 〜 0.8/0.2 である。
The organosilanetriols are obtained by hydrolyzing the corresponding hydrolyzable silanes, for example of the formula R 1 Si (OR 2 ) 3 , wherein R 2 represents an alkyl group having 1 to 4 carbon atoms. An organotrialkoxysilane represented by
It can be obtained by hydrolysis in the presence of a catalyst. Here, as R 2 , a methyl group, an ethyl group, a propyl group, a butyl group and the like are exemplified. Further, as the hydrolyzable group, a ketoxime group other than the alkoxy group, an acyloxy group, an amino group, an aminoxy group, an alkenyloxy group, a hydrolyzable silane having an amide group, a chlorine atom, and the like can be used, but handling is easy. Therefore, those having an alkoxy group as a hydrolyzable group are preferred. Examples of the hydrolysis catalyst that can be used include organic acids such as acetic anhydride, glacial acetic acid, propionic acid, citric acid, benzoic acid, formic acid, and oxalic acid; aluminum chelate compounds such as aluminum alkyl acetate; tetrachlorosilane and methyltrichlorosilane And chlorosilanes such as dimethyldichlorosilane; inorganic alkaline compounds such as aqueous ammonia; organic alkali compounds such as ethylenediamine; and amino group-containing organosilicon compounds such as γ-aminopropyltrimethoxysilane. Of these, chlorosilane is preferably used because it serves both as a raw material for silicone and a hydrolysis catalyst. Among them, methyltrichlorosilane and dimethyldichlorosilane are preferred. As raw materials for silicone, R 3 2 SiX 2 , R 4 3 SiX, SiX 4 (where R 3 and R 4 are the same substituents as R 1, and X is the same or different (Representing a functional group or a hydroxyl group) may be used. Especially of R 3 2 SiX 2 is preferable because of excellent durability of the protective coating. Molar ratio in this case organosilane triol / R 3 2 SiX 2, the abrasion resistance of the protective coating, preferably 0.9 / 0.1 or less from the detergency due from preferably 0.2 / 0.8 or higher gloss and cleaning agents of the protective film . Particularly preferably, it is 0.6 / 0.4 to 0.8 / 0.2.

【0008】また保護被膜の壁面への密着性を向上させ
るために、アミノ基、アクリル基、メタクリル基、グリ
シジル基などを有するアルコキシシランなどのシランカ
ップリング剤を、シリコーンの原料として配合してもよ
い。このようなアルコキシシランとしては、γ−アミノ
プロピルトリメトキシシラン、N−(β−アミノエチ
ル)−γ−アミノプロピルトリメトキシシランなどのア
ミノ基含有アルコキシシラン、γ−アクリロキシプロピ
ルトリメトキシシラン、γ−メタクリロキシプロピルト
リメトキシシランなどの(メタ)アクリル基含有アルコ
キシシラン、γ−グリシドキシプロピルトリメトキシシ
ランなどのグリシジル基含有アルコキシシランなどが例
示される。中でも洗浄剤による除去が良好であることか
ら、アミノ基含有アルコキシシランが好ましい。シラン
カップリング剤の配合量は、前記のシリコーン 100重量
部に対して 0.1〜5.0 重量部が好ましい。
In order to improve the adhesion of the protective film to the wall surface, a silane coupling agent such as an alkoxysilane having an amino group, an acryl group, a methacryl group, a glycidyl group or the like may be blended as a raw material of the silicone. Good. Examples of such alkoxysilanes include amino group-containing alkoxysilanes such as γ-aminopropyltrimethoxysilane, N- (β-aminoethyl) -γ-aminopropyltrimethoxysilane, γ-acryloxypropyltrimethoxysilane, γ -Alkoxysilanes containing a (meth) acryl group such as methacryloxypropyltrimethoxysilane, and alkoxysilanes containing a glycidyl group such as γ-glycidoxypropyltrimethoxysilane. Among them, amino group-containing alkoxysilanes are preferable because they are easily removed by a detergent. The amount of the silane coupling agent is preferably 0.1 to 5.0 parts by weight based on 100 parts by weight of the silicone.

【0009】縮合反応は加水分解反応後、さらに加熱攪
拌を進めることによって行われる。このようにして得ら
れるシリコーンには、一般に水酸基あるいは加水分解性
基が残存している。加水分解物であるシリコーンの重合
度は特に限定されないが、壁面への浸透性が少なく、再
補修時の保護被膜の除去が容易であることから、その粘
度が10cP以上であるものが好ましく、コーティング剤の
塗工性が良好なことから10000cP 以下が好ましい。特に
好ましくは20〜100cP である。
The condensation reaction is carried out by further heating and stirring after the hydrolysis reaction. Generally, a hydroxyl group or a hydrolyzable group remains in the thus obtained silicone. Although the degree of polymerization of the hydrolyzate silicone is not particularly limited, the viscosity is preferably 10 cP or more because the permeability to the wall surface is small and the protective film can be easily removed at the time of repair. It is preferably 10,000 cP or less because of good coating properties of the agent. Particularly preferred is 20 to 100 cP.

【0010】本発明のコーティング剤には一般に溶剤が
使用される。この溶剤成分としては前記のシリコーンを
溶解、分散するものであれば特に制限されず、メタノー
ル、エタノール、イソプロパノールのようなアルコール
類;エチレングリコールモノメチルエーテル、エチレン
グリコールモノエチルエーテル、テトラヒドロフラン、
ジオキサンのようなエーテルアルコールおよびエーテル
類;アセトン、メチルエチルケトン、ジエチルケトンの
ようなケトン類;酢酸メチル、酢酸エチル、酢酸n−ブ
チルのようなエステル類;n−ヘキサン、ガソリン、ゴ
ム揮発油、ミネラルスピリット、灯油のような脂肪族炭
化水素;ベンゼン、トルエン、キシレンのような芳香族
炭化水素;直鎖状ジメチルシロキサン、環状ジメチルシ
ロキサンのようなシリコーンオイルおよび水を例示する
ことができる。ここで水を溶媒として使用する場合は、
各種乳化剤を使用してエマルジョンとすることが好まし
い。シリコーンオイルとしては一般式(I)あるいは
(II)で示される、常温であるいは低温加熱によって揮
発性を有する低分子量のポリジメチルシロキサンが例示
される。
A solvent is generally used for the coating agent of the present invention. The solvent component is not particularly limited as long as it dissolves and disperses the silicone, and includes alcohols such as methanol, ethanol and isopropanol; ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, tetrahydrofuran,
Ether alcohols and ethers such as dioxane; ketones such as acetone, methyl ethyl ketone and diethyl ketone; esters such as methyl acetate, ethyl acetate and n-butyl acetate; n-hexane, gasoline, rubber volatile oil, mineral spirits Aliphatic hydrocarbons such as kerosene; aromatic hydrocarbons such as benzene, toluene and xylene; silicone oils such as linear dimethylsiloxane and cyclic dimethylsiloxane; and water. If water is used as the solvent here,
It is preferable to form an emulsion using various emulsifiers. Examples of the silicone oil include low molecular weight polydimethylsiloxanes represented by the general formula (I) or (II) and having volatility at room temperature or at low temperature.

【0011】[0011]

【化1】 Embedded image

【0012】これらの中でも、建築物壁面についた擦り
傷の遮蔽性が良好になり、形成される保護被膜が再補修
時に除去しやすいものとなることから、低分子量のポリ
ジメチルシロキサンを使用することが好ましい。また早
期の乾燥性が求められる場合には、メタノール、エタノ
ール、プロパノール等のアルコールを含有させることが
好ましく、特にエタノールが好ましい。これらの溶剤は
2種類以上を混合して使用してもよく、この場合、低分
子量ポリジメチルシロキサンは前記のシリコーン100 重
量部に対して 100〜500 重量部となることが好ましい。
溶剤の配合量はコーティング剤の塗布作業性から、前記
シリコーン100 重量部に対して 100〜2000重量部が好ま
しい。
Of these, low molecular weight polydimethylsiloxanes are preferred because they provide good shielding of abrasions on building walls and the protective coating formed is easy to remove during repair. preferable. When an early drying property is required, it is preferable to contain an alcohol such as methanol, ethanol or propanol, and particularly preferable is ethanol. These solvents may be used as a mixture of two or more kinds. In this case, the low molecular weight polydimethylsiloxane is preferably used in an amount of 100 to 500 parts by weight based on 100 parts by weight of the silicone.
The compounding amount of the solvent is preferably 100 to 2,000 parts by weight based on 100 parts by weight of the silicone from the viewpoint of workability of applying the coating agent.

【0013】本発明のコーティング剤には、一般に硬化
触媒が使用される。このような触媒としては縮合硬化型
シリコーン組成物に使用される一般の硬化用触媒が使用
でき、トリエタノールアミンなどの有機アミン;オクチ
ル酸スズ、オクチル酸亜鉛などのカルボン酸金属塩;ジ
ブチルスズジラウレート、ジブチルスズオクトエートな
どの有機スズ化合物;テトラブチルチタネート、テトラ
プロピルチタネートなどのチタン酸エステル;第4級ア
ンモニウムカルボキシレートなどの第4級アンモニウム
化合物;γ−アミノプロピルトリエトキシシラン、N−
(β−アミノエチル)−γ−アミノプロピルトリメトキ
シシランなどのアミン系シランカップリング剤などが例
示され、安全衛生上からジブチルスズジラウレートまた
はテトラブチルチタネートが好ましい。これらの触媒は
2種類以上を併用してもよく、アミン系シランカップリ
ング剤は保護被膜の壁面への密着性向上にも効果を示す
ため、他の触媒と併用することが好ましい。触媒の配合
量はコーティング剤の硬化速度、およびポットライフか
ら、前記シリコーン 100重量部に対して0.01〜10重量部
が好ましく、特に0.05〜2.0 重量部が好ましい。
[0013] A curing catalyst is generally used in the coating agent of the present invention. As such a catalyst, a general curing catalyst used for a condensation-curable silicone composition can be used, and an organic amine such as triethanolamine; a metal carboxylate such as tin octylate and zinc octylate; dibutyltin dilaurate; Organotin compounds such as dibutyltin octoate; titanates such as tetrabutyltitanate and tetrapropyltitanate; quaternary ammonium compounds such as quaternary ammonium carboxylate; γ-aminopropyltriethoxysilane;
Examples include amine silane coupling agents such as (β-aminoethyl) -γ-aminopropyltrimethoxysilane, and dibutyltin dilaurate or tetrabutyl titanate is preferred from the viewpoint of safety and health. Two or more of these catalysts may be used in combination, and the amine-based silane coupling agent is also effective in improving the adhesion to the wall surface of the protective coating. The amount of the catalyst is preferably from 0.01 to 10 parts by weight, particularly preferably from 0.05 to 2.0 parts by weight, based on 100 parts by weight of the silicone, in view of the curing speed of the coating agent and the pot life.

【0014】本発明のコーティング剤には、必要に応じ
て紫外線吸収剤、レベリング剤、増粘剤、顔料、染料、
抗酸化剤を配合することができる。建築物壁面への塗布
方法としては、刷毛塗り、スプレー塗り、ローラー塗り
などの方法を用いることができる。被膜の厚みは劣化部
分を遮蔽する効果、適度の被膜強度を有することから
0.5〜50μm の範囲がよく、好ましくは15〜20μm であ
る。また要すれば劣化部分のみを上記の厚み程度に、本
発明のコーティング剤で被膜形成してもよい。本発明の
コーティング剤は塗布後、数時間から数日間風乾させる
ことによって硬化し、良好な保護被膜を形成する。
The coating agent of the present invention may contain, if necessary, an ultraviolet absorber, a leveling agent, a thickener, a pigment, a dye,
Antioxidants can be included. As a coating method on the building wall, a method such as brush coating, spray coating, roller coating and the like can be used. The thickness of the coating has the effect of shielding the deteriorated part and has the appropriate coating strength.
The range is preferably from 0.5 to 50 μm, and more preferably from 15 to 20 μm. If necessary, only the deteriorated portion may be formed into a film with the coating agent of the present invention to the above-mentioned thickness. After coating, the coating agent of the present invention is cured by air drying for several hours to several days to form a good protective film.

【0015】本発明の方法で使用される洗浄剤として
は、アルカリ性洗浄剤、酸性洗浄剤が例示され、洗浄性
がよいことからアルカリ洗浄剤が好ましい。アルカリ洗
浄剤としては苛性アルカリ、ケイ酸アルカリ塩、リン酸
アルカリ塩、炭酸アルカリ塩、硼酸アルカリ塩、アルミ
ン酸アルカリ塩、アンモニア水等の無機アルカリ性化合
物、モノエタノールアミン、ジエタノールアミン、トリ
エタノールアミン、モノイソプロパノールアミン、ジイ
ソプロパノールアミン、トリイソプロパノールアミンの
ようなアルカノールアミン類、モルフォリン類、ピロリ
ドン類、ピリジン類等の有機アルカリ性化合物の水溶液
が挙げられる。本発明のコーティング剤よりなる保護被
膜は、上記洗浄剤を用いてブラシで擦るなどによって容
易に除去することができる。
Examples of the cleaning agent used in the method of the present invention include an alkaline cleaning agent and an acidic cleaning agent, and an alkali cleaning agent is preferable because of its good detergency. Examples of the alkaline cleaning agent include caustic alkali, alkali silicate, alkali phosphate, alkali carbonate, alkali borate, alkali aluminate, and inorganic alkali compounds such as ammonia water, monoethanolamine, diethanolamine, triethanolamine, and monoethanolamine. Aqueous solutions of organic alkaline compounds such as alkanolamines such as isopropanolamine, diisopropanolamine and triisopropanolamine, morpholines, pyrrolidones and pyridines. The protective film made of the coating agent of the present invention can be easily removed by rubbing with a brush using the above-mentioned cleaning agent.

【0016】[0016]

【発明の効果】本発明の方法によれば、排気ガス、酸性
雨、砂塵等の影響や塩害、凍害に対し、建築物壁面に優
れた耐磨耗性、耐候性および美観の向上を付与すること
ができ、環境問題などの観点からも実用価値は極めて大
きい。さらに本発明の方法により建築物壁面に設けられ
た保護被膜は、経時によって被膜自身の劣化が生じたと
きは、洗浄剤にて容易に剥離、洗浄が可能で、再度その
部分にコーティング剤を塗布することにより優れた耐磨
耗性、耐候性および美観の向上を付与することができる
ものであり、建築物壁面の補修が容易となるものであ
る。
According to the method of the present invention, excellent abrasion resistance, weather resistance and aesthetic appearance are imparted to a building wall against the effects of exhaust gas, acid rain, dust, salt damage and frost damage. The practical value is extremely high from the viewpoint of environmental issues. Furthermore, when the coating itself is deteriorated with the passage of time, the protective coating provided on the building wall by the method of the present invention can be easily peeled and washed with a cleaning agent, and the coating agent is applied to the portion again. By doing so, it is possible to impart excellent wear resistance, weather resistance, and improvement in aesthetic appearance, and it is easy to repair the building wall surface.

【0017】[0017]

【実施例】以下に本発明を実施例をあげて説明する。な
お、実施例中の部は重量部を、%は重量%を表し、粘度
は25℃の値を示す。
The present invention will be described below with reference to examples. In addition, the part in an Example represents a weight part,% represents weight%, and the viscosity shows the value of 25 degreeC.

【0018】合成例1 攪拌機、加温ジャケット、還流冷却器および滴下ロート
を取り付けたフラスコにメチルトリメトキシシラン1360
g (10mol) 、メタノール200gおよびメチルトリクロロシ
ランを塩酸分が50ppm となるように仕込み、攪拌しなが
ら水171g(9.5mol) を滴下ロートを使って徐々に滴下し
た。還流温度(約68〜72℃)で4時間保持して、加水分
解および縮合反応を行った。常圧、100 ℃の条件下で揮
発成分を留去した後、徐々に減圧を行い、40mmHg、 150
℃の条件下でさらに揮発成分を減圧留去して、粘度20cP
のシリコーン630g(A−1)を得た。 合成例2 表1に示す配合量のアルコキシシランおよび酢酸を、攪
拌機、加温ジャケット、還流冷却器、水分定量器および
滴下ロートを取り付けたフラスコ中に仕込み、攪拌しな
がら徐々に加熱した。液温が80℃になった時点で表1に
示す量の水を徐々に滴下して加えた。反応により生成す
るアルコールが還流する温度(約78〜83℃)で4時間保
持して、加水分解および縮合反応を行った。次に水分定
量器により留出するアルコールを除去しながら加熱攪拌
をつづけ、アルコールの留出が止まり反応液温が上昇を
示した時点で加熱を止め、常温に戻して表1に示す粘度
のシリコーン(A−2、A−3およびA−4)を得た。 合成例3 攪拌機、加温ジャケット、還流冷却器および滴下ロート
を取りつけたフラスコに、メチルトリメトキシシラン95
2g(7mol)、フェニルトリメトキシシラン198g(1mo
l)、ジメチルジクロロシラン516g(4mol)およびトルエ
ン1500mlを仕込み、攪拌しながら水234g(13mol)を徐々
に滴下した。滴下終了後、温度約110 ℃で還流させて1
時間加熱攪拌を行った。反応液を室温まで徐冷して分液
ロートに移し入れ、静置して有機層と水層に分離させた
後、下層の水層を除去してシリコーン溶液を得た。この
有機層に飽和食塩水を加えてよくかき混ぜた後、静置し
て水層を分離した。この塩析操作を2回繰り返した後、
水を加えて同様の操作で有機層を2回水洗した。この有
機層を攪拌機、加温ジャケットおよび水分定量器を取り
付けたフラスコに入れ、30mmHg、80℃で3時間揮発成分
を減圧留去して、粘度100cP のシリコーン860g(A−
5)を得た。 参考例1 容器にカルナバロウ50部、流動パラフィン25部、ポリオ
キシエチレン(10)ステアレート9部、ポリオキシエチ
レン(40)ステアレート9部、ポリオキシエチレン(1
0)オクチルフェニルエーテル12部をとり、徐々に加熱
して溶解し、90℃に保ちながら加熱攪拌した後、90℃に
加温した水 380部を徐々に加えながら1時間攪拌し、そ
の後冷却攪拌を行い、25℃まで冷却し、乳化組成物(B
−1)を得た。 参考例2 参考例1と同様に流動パラフィン33%およびプロピレン
グリコールモノステアレート12%を含有する水分散液
(B−2)を調製した。 参考例3 参考例1と同様にカルナバロウ20%、グリセリンモノラ
ウリン酸エステル5%およびポリエチレングリコール10
%を含有する水分散液(B−3)を調製した。
Synthesis Example 1 Methyltrimethoxysilane 1360 was placed in a flask equipped with a stirrer, heating jacket, reflux condenser and dropping funnel.
g (10 mol), 200 g of methanol and methyltrichlorosilane were charged so that the hydrochloric acid content was 50 ppm, and 171 g (9.5 mol) of water was gradually added dropwise using a dropping funnel while stirring. The mixture was kept at a reflux temperature (about 68 to 72 ° C.) for 4 hours to carry out hydrolysis and condensation reactions. After distilling off volatile components under the conditions of normal pressure and 100 ° C, the pressure was gradually reduced to 40 mmHg, 150
The volatile components were further distilled off under reduced pressure under the condition of
630 g (A-1) of silicone was obtained. Synthesis Example 2 The amounts of alkoxysilane and acetic acid shown in Table 1 were charged into a flask equipped with a stirrer, a heating jacket, a reflux condenser, a moisture meter, and a dropping funnel, and gradually heated while stirring. When the liquid temperature reached 80 ° C., the amount of water shown in Table 1 was gradually added dropwise. The hydrolysis and condensation reaction were carried out while maintaining the temperature at which the alcohol generated by the reaction was refluxed (about 78 to 83 ° C) for 4 hours. Next, heating and stirring were continued while removing the alcohol distilled off by the water quantifier. When the distillation of the alcohol was stopped and the temperature of the reaction solution was increased, the heating was stopped, the temperature was returned to room temperature, and the silicone having the viscosity shown in Table 1 was returned. (A-2, A-3 and A-4) were obtained. Synthesis Example 3 A flask equipped with a stirrer, a heating jacket, a reflux condenser and a dropping funnel was charged with methyltrimethoxysilane 95.
2 g (7 mol), 198 g of phenyltrimethoxysilane (1 mol
l), 516 g (4 mol) of dimethyldichlorosilane and 1500 ml of toluene were charged, and 234 g (13 mol) of water was gradually added dropwise with stirring. After completion of the dropwise addition, the mixture was refluxed at a temperature of about 110 ° C. for 1 hour.
Heating and stirring were performed for hours. The reaction solution was gradually cooled to room temperature, transferred to a separating funnel, allowed to stand and separated into an organic layer and an aqueous layer, and the lower aqueous layer was removed to obtain a silicone solution. A saturated saline solution was added to the organic layer and the mixture was stirred well, and then allowed to stand to separate an aqueous layer. After repeating this salting-out operation twice,
Water was added and the organic layer was washed twice with the same operation. This organic layer was placed in a flask equipped with a stirrer, a heating jacket and a water content meter, and volatile components were distilled off under reduced pressure at 30 mmHg and 80 ° C. for 3 hours.
5) was obtained. Reference Example 1 In a container, 50 parts of carnauba wax, 25 parts of liquid paraffin, 9 parts of polyoxyethylene (10) stearate, 9 parts of polyoxyethylene (40) stearate, and polyoxyethylene (1 part)
0) Take 12 parts of octyl phenyl ether, gradually heat and dissolve, stir while heating at 90 ° C, stir for 1 hour while gradually adding 380 parts of water heated to 90 ° C, then cool and stir And cooled to 25 ° C. to obtain an emulsion composition (B
-1) was obtained. Reference Example 2 In the same manner as in Reference Example 1, an aqueous dispersion (B-2) containing 33% of liquid paraffin and 12% of propylene glycol monostearate was prepared. Reference Example 3 As in Reference Example 1, carnauba wax 20%, glycerin monolaurate 5% and polyethylene glycol 10
% Of an aqueous dispersion (B-3).

【0019】実施例1〜9および比較例1〜3 表2に示す配合組成でコーティング剤を調製し、遮蔽
性、耐候性、耐水性、洗浄性および美観を下記の方法で
評価した。結果を表2に示す。 〔試験片の作成〕15×15cmの大きさの白色タイル板を、
サンドペーパーで軽く擦って擦り傷をつけた。これにエ
アーガンを用いてコーティング剤を吹付け、1日風乾し
て保護被膜を形成させ試験片を作成した。 〔遮蔽性〕試験片の外観を目視にて観察し下記4段階で
評価した。 ◎:擦り傷部分が良く遮蔽され、被膜の透明感も良好。 ○:擦り傷部分の一部分が露出しているが、被膜の透明
感は良好。 △:擦り傷部分の一部分が露出し、被膜の透明感もやや
不良。 ×:遮蔽効果不十分で、被膜の透明感もない。 〔耐水性〕試験片の上に水道水を14時間流した後、外観
を目視にて観察し下記4段階で評価した。 ◎:擦り傷部分が良く遮蔽され、被膜の透明感も良好。 ○:擦り傷部分の一部分が露出しているが、被膜の透明
感は良好。 △:擦り傷部分の一部分が露出し、被膜の透明感もやや
不良。 ×:遮蔽効果不十分で、被膜の透明感もない。 〔耐候性〕サンシャインウエザーメーターを用いて500
時間暴露した後、外観を目視にて観察し下記4段階で評
価した。 ◎:擦り傷部分が良く遮蔽され、被膜の透明感も良好。 ○:擦り傷部分の一部分が露出しているが、被膜の透明
感は良好。 △:擦り傷部分の一部分が露出し、被膜の透明感もやや
不良。 ×:遮蔽効果不十分で、被膜の透明感もない。 〔美観〕試験片を25℃、相対湿度60%の条件下で2か月
間静置した後、外観を目視にて観察し下記4段階で評価
した。 ◎:被膜の透明感は良好で、埃の付着もない。 ○:被膜の透明感は良好だが、埃の付着が一部みられ
る。 △:被膜の透明感がやや不良で、埃の付着も一部みられ
る。 ×:被膜の透明感が不良で、埃の付着もみられる。 〔洗浄性〕試験片を2%水酸化ナトリウム水溶液中に30
分間浸漬後、水洗して保護被膜の残存状態を下記4段階
で評価した。 ◎:被膜が完全に除去される。 ○:ごく一部に被膜が残存するが、さらに10分間の浸漬
で完全に除去される。 △:一部に被膜が残存するが、さらに20分間の浸漬で完
全に除去される。 ×:被膜の大部分が残存し、さらに20分間の浸漬でも残
存被膜が認められる。
Examples 1 to 9 and Comparative Examples 1 to 3 Coating agents were prepared according to the composition shown in Table 2, and the shielding properties, weather resistance, water resistance, detergency, and appearance were evaluated by the following methods. Table 2 shows the results. [Preparation of test piece] A white tile board of 15 × 15 cm in size,
Scratched lightly with sandpaper. This was sprayed with a coating agent using an air gun and air-dried for one day to form a protective film, thereby preparing a test piece. [Shielding Property] The appearance of the test piece was visually observed and evaluated according to the following four grades. :: The abrasion portion is well shielded, and the transparency of the coating is good. :: A part of the scratch portion is exposed, but the transparency of the coating is good. Δ: A part of the abrasion part was exposed, and the transparency of the coating was slightly poor. ×: Insufficient shielding effect and no transparency of the film. [Water resistance] After running tap water for 14 hours on the test piece, the appearance was visually observed and evaluated according to the following four grades. :: The abrasion portion is well shielded, and the transparency of the coating is good. :: A part of the scratch portion is exposed, but the transparency of the coating is good. Δ: A part of the abrasion part was exposed, and the transparency of the coating was slightly poor. ×: Insufficient shielding effect and no transparency of the film. [Weather resistance] 500 using sunshine weather meter
After exposure for a period of time, the appearance was visually observed and evaluated according to the following four grades. :: The abrasion portion is well shielded, and the transparency of the coating is good. :: A part of the scratch portion is exposed, but the transparency of the coating is good. Δ: A part of the abrasion part was exposed, and the transparency of the coating was slightly poor. ×: Insufficient shielding effect and no transparency of the film. [Aesthetics] After the test piece was allowed to stand for 2 months at 25 ° C. and a relative humidity of 60%, the appearance was visually observed and evaluated according to the following four grades. A: The transparency of the film is good and there is no adhesion of dust. :: The transparency of the coating is good, but some dust adhesion is observed. Δ: Transparency of the coating film was slightly poor, and some dust adhered. ×: The transparency of the coating film was poor, and adhesion of dust was observed. [Washability] A test piece was placed in a 2% aqueous sodium hydroxide solution for 30 minutes.
After immersion for 5 minutes, it was washed with water and the remaining state of the protective film was evaluated according to the following four grades. A: The coating is completely removed. :: The coating remains on a very small portion, but is completely removed by further immersion for 10 minutes. Δ: The coating remains partially, but is completely removed by further immersion for 20 minutes. ×: Most of the coating remained, and the remaining coating was observed even after immersion for 20 minutes.

【0020】[0020]

【表1】 [Table 1]

【0021】[0021]

【表2】 [Table 2]

【0022】表2に示したとおり、本発明の方法に用い
るコーティング剤は、いずれも耐水性、美観の向上など
の各特性について良好な結果を示した。一方、比較例の
コーティング剤では水溶性を有するため、耐水性に劣る
とともに、耐候性についても十分満足する結果が得られ
なかった。
As shown in Table 2, each of the coating agents used in the method of the present invention showed good results with respect to each property such as improvement of water resistance and aesthetic appearance. On the other hand, since the coating agent of the comparative example has water solubility, it was inferior in water resistance and could not obtain a sufficiently satisfactory result on weather resistance.

【0023】実施例10 白色タイル板のかわりに、ステンレス板、磨き加工した
みかげ石、アクリルリシン吹付けPCパネルを使用し、
実施例6のコーティング剤を使用して同様に評価した。
遮蔽性、耐水性、耐候性、美観および洗浄性とも良好な
結果を示した。
Example 10 Instead of a white tile plate, a stainless steel plate, polished granite, and an acrylic lysine sprayed PC panel were used.
The same evaluation was performed using the coating agent of Example 6.
Good results were obtained in all of the shielding properties, water resistance, weather resistance, aesthetic appearance and detergency.

フロントページの続き (58)調査した分野(Int.Cl.6,DB名) E04G 23/02 C09K 3/18 104Continuation of the front page (58) Field surveyed (Int.Cl. 6 , DB name) E04G 23/02 C09K 3/18 104

Claims (8)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 建築物の壁面に洗浄剤で除去が可能な、
シリコーンを主成分とするコーティング剤を塗布するこ
とを特徴とする建築物壁面の補修方法。
1. A wall of a building that can be removed with a cleaning agent.
A method for repairing a building wall, comprising applying a coating agent containing silicone as a main component.
【請求項2】 洗浄剤がアルカリ洗浄剤である請求項1
記載の補修方法。
2. The cleaning agent according to claim 1, wherein the cleaning agent is an alkaline cleaning agent.
Repair method described.
【請求項3】 シリコーンがオルガノシラントリオール
またはその部分縮合物を主成分とするシランまたはシロ
キサンの縮合物である請求項1記載の補修方法。
3. The repair method according to claim 1, wherein the silicone is a silane or siloxane condensate containing organosilanetriol or a partial condensate thereof as a main component.
【請求項4】 コーティング剤が (A) シリコーン 100重量部 (B) 硬化触媒 0.01〜10重量部 (C) 溶剤 100〜2000重量部 よりなる請求項3記載の補修方法。4. The repair method according to claim 3, wherein the coating agent comprises (A) 100 parts by weight of silicone (B) 0.01 to 10 parts by weight of a curing catalyst (C) 100 to 2000 parts by weight of a solvent. 【請求項5】 溶剤が揮発性ポリシロキサンである請求
項4記載の補修方法。
5. The repair method according to claim 4, wherein the solvent is a volatile polysiloxane.
【請求項6】 硬化触媒がアミノ基含有アルコキシシラ
ンである請求項4記載の補修方法。
6. The repair method according to claim 4, wherein the curing catalyst is an amino group-containing alkoxysilane.
【請求項7】 シリコーンの粘度が10〜10000cP である
請求項4記載の補修方法。
7. The repair method according to claim 4, wherein the silicone has a viscosity of 10 to 10,000 cP.
【請求項8】 建築物の壁面が非多孔質材料よりなるも
のである請求項1記載の補修方法。
8. The repair method according to claim 1, wherein the wall of the building is made of a non-porous material.
JP27547891A 1991-10-23 1991-10-23 Repair method of building wall Expired - Lifetime JP2790929B2 (en)

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Publication Number Publication Date
JPH05113041A JPH05113041A (en) 1993-05-07
JP2790929B2 true JP2790929B2 (en) 1998-08-27

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JP2005350892A (en) * 2004-06-08 2005-12-22 Panahome Corp Repair method for painted surface of exterior wall, and exterior wall painting structure
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