JPH06256975A - Water repellent corrosion preventive layer and corrosion preventive treating material therefor - Google Patents

Water repellent corrosion preventive layer and corrosion preventive treating material therefor

Info

Publication number
JPH06256975A
JPH06256975A JP7096793A JP7096793A JPH06256975A JP H06256975 A JPH06256975 A JP H06256975A JP 7096793 A JP7096793 A JP 7096793A JP 7096793 A JP7096793 A JP 7096793A JP H06256975 A JPH06256975 A JP H06256975A
Authority
JP
Japan
Prior art keywords
coating
liquid
cross
linking
silicone rubber
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
JP7096793A
Other languages
Japanese (ja)
Other versions
JP3172318B2 (en
Inventor
Satoru Gunji
悟 郡司
Kazumasa Asano
一正 浅野
Naoki Miwa
直樹 三輪
Tetsuo Fujimoto
哲夫 藤本
Shuji Chiba
修二 千葉
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.)
Nitto Denko Corp
Momentive Performance Materials Japan LLC
Original Assignee
Nitto Denko Corp
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
Application filed by Nitto Denko Corp, Toshiba Silicone Co Ltd filed Critical Nitto Denko Corp
Priority to JP07096793A priority Critical patent/JP3172318B2/en
Publication of JPH06256975A publication Critical patent/JPH06256975A/en
Application granted granted Critical
Publication of JP3172318B2 publication Critical patent/JP3172318B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Protection Of Pipes Against Damage, Friction, And Corrosion (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

PURPOSE:To enable the easy formation of the tough corrosion preventive layer having excellent water repellency, heat resistance and adhesion property on a work site at a low temp. by coating a metal, etc., with a cold cross-linking type coating material formed by impregnating a porous base material with a prescribed liquid intimate mixture. CONSTITUTION:The metallic surface, etc., are coated with the cold cross-linking type coating material. The water repellent corrosion preventive layer having <=35dyn/cm surface temp. is formed by cross-linking this coating layer with a coating liquid for cross-linking. The cold cross-linking type coating material mentioned above is formed by using uncross-linked liquid silicone rubber as an essential component and impregnating the porous base material with the liquid intimate mixture contg. a hardener, etc. The coating liquid for cross- linking mentioned above contains the uncross-linked liquid silicone rubber and/or silicone oil as essential components and contains either the hardener mentioned above or hardening catalyst.

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、室温で簡便に密着性よ
く施工できて金属の腐食防止処理に好適な撥水性防食層
及びその防食処理材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a water-repellent anticorrosive layer which can be easily applied at room temperature with good adhesion and is suitable for the anticorrosion treatment of metals, and its anticorrosion treatment material.

【0002】[0002]

【従来の技術】従来、生産ラインによる加熱塗覆方式で
金属表面に熱溶融ポリエチレンやエポキシ樹脂をライニ
ングしてなる防食層が知られていた。しかしながら、ラ
イニングに煩雑な処理操作と大量の熱量が要求されるう
えに保管時や運搬時に形成防食層が外的要因で損傷しや
すく、防食部品の接続部、例えばパイプラインの接続部
へのライニング処理が困難な問題点があった。
2. Description of the Related Art Conventionally, there has been known an anticorrosion layer formed by lining a metal surface with hot-melt polyethylene or an epoxy resin by a heating coating method on a production line. However, the lining requires complicated processing operations and a large amount of heat, and the formed anticorrosion layer is easily damaged by external factors during storage and transportation, and the lining to the connection part of the anticorrosion parts, for example, the connection part of the pipeline There was a problem that it was difficult to process.

【0003】一方、大量の熱量を要しない冷工法で形成
できて現場施工に有利な防食層としては、金属表面にウ
レタン樹脂やエポキシ樹脂を塗布してなる重合硬化皮膜
が知られていた。しかしながら、塗膜厚がバラツキやす
くて均一な防食層を形成しにくく、二液タイプの塗布液
の場合には混合比のバラツキで皮膜の物性が不均一とな
り均質な防食層を形成しにくい問題点があった。
On the other hand, as an anticorrosion layer which can be formed by a cooling method which does not require a large amount of heat and is advantageous for on-site construction, a polymerized and cured film formed by coating a urethane resin or an epoxy resin on a metal surface has been known. However, it is difficult to form a uniform anticorrosion layer because the coating thickness varies, and in the case of a two-component type coating solution, the physical properties of the coating become uneven due to the variation of the mixing ratio, making it difficult to form a uniform anticorrosion layer. was there.

【0004】他方、厚さや均質さの良好な防食層として
は、フィルム等の防食基材に感圧接着層を設けた防食テ
ープを金属表面に巻回ないし接着したものが知られてい
た。しかしながら、外気温や外圧で防食テープが変形し
やすくて防食層にシワや浮きが発生しやすく、またゴミ
や埃等が付着して汚染されやすい問題点があった。
On the other hand, as an anticorrosion layer having good thickness and homogeneity, it is known that an anticorrosion tape having a pressure-sensitive adhesive layer provided on an anticorrosion substrate such as a film is wound or adhered on a metal surface. However, there is a problem that the anticorrosion tape is easily deformed due to the outside air temperature and the outside pressure, wrinkles and floats are likely to occur in the anticorrosion layer, and dust and dirt are easily attached and contaminated.

【0005】[0005]

【発明が解決しようとする課題】本発明は、ライニング
処理の如く煩雑な処理操作や大量の熱量を要することな
く作業現場でも簡便に室温等の低温で施工できて防食部
品の接続部の処理も容易であり、形成防食層が厚さや物
性の均一性に優れると共に外的要因で損傷や変形を起こ
しにくい強靱さを有してシワや浮きが発生しにくくゴミ
や埃等で汚染されにくい撥水性防食層を得ることを課題
とする。
DISCLOSURE OF THE INVENTION The present invention can be easily applied at a work site at a low temperature such as room temperature without requiring a complicated processing operation such as a lining processing and a large amount of heat, and can also process a connection portion of an anticorrosion component. Easy to use, the anticorrosive layer has excellent thickness and uniformity of physical properties, and it has a toughness that does not easily cause damage or deformation due to external factors. It is unlikely to cause wrinkles or floating, and is unlikely to be contaminated with dirt or dust. The task is to obtain an anticorrosion layer.

【0006】[0006]

【課題を解決するための手段】本発明は、未架橋液状シ
リコーンゴムを主成分とし硬化剤又は硬化触媒の一方を
含有する液状混和物を多孔性基材に含浸させてなる室温
架橋型被覆材を金属表面又は防食欠陥部に被覆施与して
被覆層を形成し、その被覆層を、未架橋液状シリコーン
ゴム及び/又はシリコーンオイルを主成分とし前記の硬
化剤又は硬化触媒の他方を含有する架橋用塗液で架橋さ
せたことを特徴とする撥水性防食層、及び前記の室温架
橋型被覆材と架橋用塗液とからなることを特徴とする撥
水性防食処理材を提供するものである。
DISCLOSURE OF THE INVENTION The present invention is a room temperature cross-linking type coating material obtained by impregnating a porous base material with a liquid mixture containing an uncross-linked liquid silicone rubber as a main component and containing either a curing agent or a curing catalyst. Is applied to the metal surface or the anticorrosion defect portion to form a coating layer, and the coating layer contains an uncrosslinked liquid silicone rubber and / or silicone oil as a main component and the other of the above-mentioned curing agent or curing catalyst. The present invention provides a water-repellent anticorrosive layer characterized by being cross-linked with a cross-linking coating liquid, and a water-repellent anti-corrosion treatment material comprising the above room temperature cross-linking type coating material and a cross-linking coating liquid. .

【0007】[0007]

【作用】上記構成の室温架橋型被覆材は、含有の液状混
和物を介して金属表面等の被覆面に対し粗面や曲面であ
る場合にも充分な濡れ性や変形性を示して良好に密着す
る。また硬化剤と硬化触媒の分離で安定した長期保存が
可能となると共に、架橋用塗液の施与でそれが室温架橋
型被覆材の被覆層中に浸透し前記液状混和物中の未架橋
液状シリコーンゴムと硬化剤とが硬化触媒の作用の下に
反応して室温等で架橋し、金属等に強固に接着しつつ多
孔性基材と共に強靱な撥水性の防食層を形成する。
The room-temperature cross-linking type coating material having the above-mentioned structure shows satisfactory wettability and deformability even when it is a rough surface or a curved surface with respect to the coating surface such as a metal surface through the contained liquid mixture. In close contact. In addition, the curing agent and curing catalyst can be separated for stable long-term storage, and the application of the cross-linking coating liquid allows it to penetrate into the coating layer of the room temperature cross-linking type coating material, and the uncross-linked liquid in the liquid mixture. The silicone rubber and the curing agent react under the action of a curing catalyst to crosslink at room temperature or the like, firmly bonding to a metal or the like and forming a tough water-repellent anticorrosion layer together with the porous substrate.

【0008】前記の結果、厚さや物性の均一性に優れる
防食層を作業現場でも簡便に低温施工で形成でき、パイ
プライン等の接続部も容易に処理できる。また液状シリ
コーンゴムの架橋反応を利用した硬化機構であるので防
食層形成時に有害な有機溶剤等の関与を回避でき、数時
間程度の短時間でタックフリーな状態に硬化してゴミや
埃等で汚染されにくいうえに表面張力も小さくて水垢等
も付着しにくく光沢のある美観に優れる状態を持続す
る。さらに形成される防食層は外的要因で損傷や変形を
起こしにくくシワや浮きが発生しにくくて撥水性の防食
効果を長期に持続する。
As a result of the above, an anticorrosion layer having excellent thickness and uniformity of physical properties can be easily formed at a work site at a low temperature, and a connecting portion such as a pipeline can be easily treated. In addition, since it is a curing mechanism that uses the crosslinking reaction of liquid silicone rubber, it is possible to avoid the involvement of harmful organic solvents during the formation of the anticorrosion layer, and to cure it in a tack-free state in a short time of about several hours to prevent dust and dirt. In addition to being less likely to be contaminated, the surface tension is also small, and water stains etc. are hard to adhere, and it maintains a glossy and excellent appearance. Furthermore, the formed anticorrosion layer is unlikely to be damaged or deformed due to external factors, and is unlikely to be wrinkled or floated, so that the water-repellent anticorrosion effect is maintained for a long time.

【0009】[0009]

【実施例】本発明において用いる室温架橋型被覆材は、
未架橋液状シリコーンゴムを主成分とし硬化剤又は硬化
触媒の一方を含有する液状混和物を柔軟な多孔性基材に
含浸させたものである。また架橋用塗液は、未架橋液状
シリコーンゴム及び/又はシリコーンオイルを主成分と
し前記の硬化剤又は硬化触媒の他方を含有させたもので
ある。
EXAMPLES Room temperature crosslinkable coating materials used in the present invention are
A flexible porous substrate is impregnated with a liquid mixture containing an uncrosslinked liquid silicone rubber as a main component and one of a curing agent and a curing catalyst. The cross-linking coating liquid contains an uncross-linked liquid silicone rubber and / or silicone oil as a main component and contains the other of the above-mentioned curing agents or curing catalysts.

【0010】液状混和物は、未架橋液状シリコーンゴム
すなわち液状ポリオルガノシロキサンを主成分とし、硬
化剤又は硬化触媒を含有して縮合反応型又は付加反応型
などの硬化機構で硬化してゴム状の硬化物となるもので
ある。
The liquid mixture contains an uncrosslinked liquid silicone rubber, that is, liquid polyorganosiloxane as a main component, contains a curing agent or a curing catalyst, and is cured by a condensation reaction type or addition reaction type curing mechanism to give a rubber-like mixture. It is a cured product.

【0011】前記の未架橋液状シリコーンゴムとして
は、一般単位式:RaSiO(4-a)/2(式中、Rは置換も
しくは非置換の1価の炭化水素基又は水酸基、aは1〜
3の整数である。)で表される構成単位からなる単一重
合体、もしくは共重合体、又はこれらの混合物を用いる
ことができる。
The above-mentioned uncrosslinked liquid silicone rubber has a general unit formula: R a SiO (4-a) / 2 (wherein R is a substituted or unsubstituted monovalent hydrocarbon group or hydroxyl group, and a is 1). ~
It is an integer of 3. A homopolymer, a copolymer, or a mixture thereof composed of the structural unit represented by the formula (1) can be used.

【0012】上記の式中、基Rの置換もしくは非置換の
1価の炭化水素基は、同一であってもよいし、異なって
いてもよく、例えばメチル基、エチル基、プロピル基、
ブチル基、ヘキシル基、ドデシル基等のアルキル基、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、ベンジル基、β−フェニルエチル
基、β−フェニルプロピル基等のアラルキル基、3,
3,3−トリフルオロプロピル基、クロロメチル基等の
1価の置換炭化水素基等をあげることができ、これらは
未架橋液状シリコーンゴム(液状ポリオルガノシロキサ
ン)の合成の容易さやその硬化機構及び組成物の流動
性、さらには組成物の硬化物の例えば耐熱性等の物理的
性質に応じて適宜選択することができる。
In the above formula, the substituted or unsubstituted monovalent hydrocarbon groups of the group R may be the same or different, for example, a methyl group, an ethyl group, a propyl group,
Alkyl groups such as butyl group, hexyl group, dodecyl group, alkenyl groups such as vinyl group, allyl group, aryl groups such as phenyl group, tolyl group, benzyl group, β-phenylethyl group, β-phenylpropyl group, etc. aralkyl Base, 3,
Examples thereof include monovalent substituted hydrocarbon groups such as 3,3-trifluoropropyl group and chloromethyl group, which are easy to synthesize an uncrosslinked liquid silicone rubber (liquid polyorganosiloxane) and a curing mechanism thereof. It can be appropriately selected depending on the fluidity of the composition and the physical properties of the cured product of the composition such as heat resistance.

【0013】用いる未架橋液状シリコーンゴムは、常温
で液状であればその分子構造は特に限定されず、直鎖
状、分岐状、網状もしくは僅かに三次元網状構造を有す
るもの、又はこれらが混在した状態のものであっても何
ら差し支えないが、25℃における粘度が100〜10
0,000cStのものが好ましく、1,000〜5
0,000cStのものがさらに好ましい。
The uncrosslinked liquid silicone rubber used is not particularly limited in its molecular structure as long as it is liquid at room temperature, and has a linear, branched, reticulated or slightly three-dimensional reticulated structure, or a mixture thereof. Although there is no problem even if it is in a state, the viscosity at 25 ° C is 100 to 10
50,000 cSt is preferable, and 1,000 to 5
It is more preferably 10,000 cSt.

【0014】前記の粘度が100cSt未満では、組成
物の硬化物に優れた機械的性質を付与することが困難で
あり、また100,000cStを超える場合は、組成
物に適度な流動性を付与することができない。
When the viscosity is less than 100 cSt, it is difficult to impart excellent mechanical properties to the cured product of the composition, and when it exceeds 100,000 cSt, the composition is imparted with appropriate fluidity. I can't.

【0015】液状混和物の調製は、未架橋液状シリコー
ンゴムと硬化剤又は硬化触媒の一方を混合することによ
り行うことができる。硬化剤は、硬化触媒の存在下に室
温等の低温で未架橋液状シリコーンゴムや架橋用塗液の
主成分であるシリコーンオイルと反応して未架橋液状シ
リコーンゴムや架橋用塗液のシリコーンオイルと架橋す
るものである。
The liquid mixture can be prepared by mixing the uncrosslinked liquid silicone rubber with one of the curing agent and the curing catalyst. The curing agent reacts with the uncrosslinked liquid silicone rubber or the silicone oil which is the main component of the crosslinking coating liquid at a low temperature such as room temperature in the presence of a curing catalyst to form the uncrosslinked liquid silicone rubber or the silicone oil of the crosslinking coating liquid. It crosslinks.

【0016】未架橋液状シリコーンゴムや硬化剤又は硬
化触媒としては、室温等の低温で硬化するように、その
縮合反応型や付加反応型などの硬化機構に応じて適宜な
組合せで用いることができる。
The uncrosslinked liquid silicone rubber, the curing agent or the curing catalyst can be used in an appropriate combination so as to cure at a low temperature such as room temperature depending on the condensation reaction type or addition reaction type curing mechanism. .

【0017】ちなみに縮合反応型の液状混和物の場合
は、未架橋液状シリコーンゴムとして(a)分子鎖末端
がシラノール基又はアルコキシ基で封鎖されたポリオル
ガノシロキサンを用い、硬化剤として(b)ケイ素原子
に結合した加水分解性基を一分子中に少なくとも3個有
する有機ケイ素化合物、又は硬化触媒を配合する。
By the way, in the case of a condensation reaction type liquid mixture, (a) a polyorganosiloxane having a molecular chain terminal blocked with a silanol group or an alkoxy group is used as the uncrosslinked liquid silicone rubber, and (b) silicon is used as a curing agent. An organosilicon compound having at least three hydrolyzable groups bonded to atoms in one molecule, or a curing catalyst is added.

【0018】(a)成分のポリオルガノシロキサン中の
ケイ素原子に結合する置換又は非置換の1価の炭化水素
基の中でも、合成の容易さからメチル基、ビニル基もし
くはフェニル基が好ましい。さらにはケイ素原子に結合
する炭化水素基がメチル基である場合が、他の炭化水素
基の場合と比較して原料中間体の合成が容易であり、得
られる重合体の重合度の高さに比べて粘度が最も低く、
また硬化物である弾性体の物性のバランスに好影響を与
えるため最も好ましい。
Among the substituted or unsubstituted monovalent hydrocarbon groups bonded to the silicon atom in the polyorganosiloxane of the component (a), a methyl group, a vinyl group or a phenyl group is preferable from the viewpoint of easy synthesis. Furthermore, when the hydrocarbon group bonded to the silicon atom is a methyl group, the synthesis of the raw material intermediate is easier than in the case of other hydrocarbon groups, and the degree of polymerization of the resulting polymer is high. Has the lowest viscosity,
Further, it is most preferable because it has a favorable effect on the balance of the physical properties of the elastic body which is a cured product.

【0019】従って、実質的に全てがメチル基であるこ
とが最も好ましいが、硬化物に耐熱性が要求される場合
はケイ素原子に結合する炭化水素基のうち、一部がフェ
ニル基であることが好ましい。このようにメチル基以外
の炭化水素基を含有する場合においても上述した理由か
ら、重合体中の全炭化水素基数の85%以上がメチル基
であることが好ましい。
Therefore, it is most preferable that substantially all of them are methyl groups, but when the cured product is required to have heat resistance, a part of the hydrocarbon groups bonded to the silicon atom is a phenyl group. Is preferred. Even in the case of containing a hydrocarbon group other than a methyl group, it is preferable that 85% or more of the total number of hydrocarbon groups in the polymer is a methyl group, for the reason described above.

【0020】(b)成分の有機ケイ素化合物としては、
ケイ素原子に結合した加水分解性基を一分子中に少なく
とも3個有するものであれば如何なるものであってもよ
く、例えばシラン化合物もしくはその部分加水分解縮合
物、直鎖状ポリオルガノシロキサン又は環状ポリオルガ
ノシロキサンを用いることができる。
As the organosilicon compound as the component (b),
Any one may be used as long as it has at least three hydrolyzable groups bonded to a silicon atom in one molecule. For example, a silane compound or a partially hydrolyzed condensate thereof, a linear polyorganosiloxane or a cyclic poly Organosiloxanes can be used.

【0021】有機ケイ素化合物中のケイ素原子に結合す
る加水分解性基としては、アルコキシ基、アシロキシ
基、N,N−ジアルキルアミノ基、N−アルキルアミド
基、N,N−ジアルキルアミノキシ基、ケトオキシム
基、アルケノキシ基などをあげることができる。
Examples of the hydrolyzable group bonded to the silicon atom in the organosilicon compound include an alkoxy group, an acyloxy group, an N, N-dialkylamino group, an N-alkylamide group, an N, N-dialkylaminoxy group and a ketoxime. Group, alkenoxy group and the like.

【0022】また有機ケイ素化合物においてケイ素原子
には、上記した加水分解性基以外に例えばメチル基、エ
チル基、プロピル基、ブチル基等のアルキル基、ビニル
基、アリル基等のアルケニル基、フェニル基等のアリー
ル基、3,3,3−トリフルオロプロピル基、クロロメ
チル基等のハロアルキル基などの置換又は非置換の1価
の炭化水素基が結合していてもよい。
In addition to the above-mentioned hydrolyzable groups, the organic silicon compounds may have, in addition to the above-mentioned hydrolyzable groups, alkyl groups such as methyl group, ethyl group, propyl group and butyl group, alkenyl groups such as vinyl group and allyl group, and phenyl group. Or the like, a substituted or unsubstituted monovalent hydrocarbon group such as an aryl group, a 3,3,3-trifluoropropyl group, a haloalkyl group such as a chloromethyl group may be bonded.

【0023】かかる(b)成分は、ケイ素原子に結合し
た加水分解性基が(a)成分中のシラノール基又はアル
コキシ基の当量以上になるように配合することが好まし
い。(b)成分の配合量が過少では(a)成分の縮合反
応が充分に進行しない。
The component (b) is preferably blended so that the hydrolyzable group bonded to the silicon atom is equivalent to or more than the silanol group or alkoxy group in the component (a). If the blending amount of the component (b) is too small, the condensation reaction of the component (a) will not proceed sufficiently.

【0024】一方、縮合反応を促進するための硬化触媒
としては、有機カルボン酸の金属塩、例えば酢酸、オク
タン酸、ラウリン酸、ステアリン酸、オレイン酸、ナフ
テン酸、安息香酸等のカルボン酸と、スズ、亜鉛、鉛、
鉄、アンチモン、バリウム、チタン、マンガン等の金属
との塩などをあげることができる。
On the other hand, as a curing catalyst for promoting the condensation reaction, a metal salt of an organic carboxylic acid, for example, a carboxylic acid such as acetic acid, octanoic acid, lauric acid, stearic acid, oleic acid, naphthenic acid or benzoic acid, Tin, zinc, lead,
Examples thereof include salts with metals such as iron, antimony, barium, titanium and manganese.

【0025】また前記以外にも例えば、ジブチルスズジ
アセテート、ジブチルスズジオクトエート、ジブチルス
ズジラウレート、水酸化ジメチルスズオレエート、ジブ
チルスズオレエート、ジフェニルスズジアセテート、酸
化ジブチルスズ、ジブチルスズジメトキシド等の有機ス
ズ化合物、テトラプロピルチタネート、テトラブチルチ
タネート、テトラオクチルチタネート等の有機チタン酸
エステル、ジイソプロポキシ(アセチルアセトナト)チ
タン、ジイソプロピルビス(エチルアセトアセタト)チ
タン、1,3−プロピレンジオキシビス(アセチルアセ
トナト)チタン、1,3−プロピレンジオキシビス(エ
チルアセトアセタト)チタン等のチタンキレート化合物
等の有機金属化合物などもあげることができる。
In addition to the above, for example, organic tin compounds such as dibutyltin diacetate, dibutyltin dioctoate, dibutyltin dilaurate, dimethyltin oleate hydroxide, dibutyltin oleate, diphenyltin diacetate, dibutyltin oxide, dibutyltin dimethoxide; Organic titanate esters such as propyl titanate, tetrabutyl titanate, tetraoctyl titanate, diisopropoxy (acetylacetonato) titanium, diisopropylbis (ethylacetoacetato) titanium, 1,3-propylenedioxybis (acetylacetonato) Other examples include organic metal compounds such as titanium chelate compounds such as titanium and 1,3-propylenedioxybis (ethylacetoacetato) titanium.

【0026】このような縮合反応型の液状混和物の場
合、未架橋液状シリコーンゴムは、硬化剤及び硬化触媒
(場合により不要のこともある。)の存在下、空気中等
の湿気に触れることで加水分解され、架橋反応が進行し
てゴム状に硬化する。
In the case of such a condensation reaction type liquid mixture, the uncrosslinked liquid silicone rubber is exposed to moisture in the air in the presence of a curing agent and a curing catalyst (which may be unnecessary in some cases). It is hydrolyzed, the crosslinking reaction proceeds, and it is cured into a rubber.

【0027】一方、付加反応型の液状混和物の場合は、
未架橋液状シリコーンゴムとして(c)ケイ素原子に結
合したアルケニル基を一分子中に少なくとも2個有する
ポリオルガノシロキサンを用い、硬化剤として(d)オ
ルガノハイドロジェンシラン又はポリオルガノハイドロ
ジェンシロキサン、又は付加反応用の硬化触媒を配合す
る。また硬化してゲル状物になるものを得ようとする場
合には、(c)成分としてケイ素原子に結合したアルケ
ニル基を一分子中に1個有するポリオルガノシロキサン
を併用することもできる。
On the other hand, in the case of an addition reaction type liquid mixture,
As the uncrosslinked liquid silicone rubber, (c) a polyorganosiloxane having at least two alkenyl groups bonded to silicon atoms in one molecule is used, and (d) an organohydrogensilane or polyorganohydrogensiloxane as a curing agent, or addition. A curing catalyst for the reaction is added. Further, when it is desired to obtain a gelled product by curing, a polyorganosiloxane having one alkenyl group bonded to a silicon atom in one molecule can be used in combination as the component (c).

【0028】(c)成分のポリオルガノシロキサンに含
有されているアルケニル基としては、例えばビニル基、
アリル基、1−ブテニル基、1−ヘキセニル基などをあ
げることができ、合成の容易さからビニル基が好まし
い。
Examples of the alkenyl group contained in the component (c) polyorganosiloxane include a vinyl group,
An allyl group, a 1-butenyl group, a 1-hexenyl group and the like can be mentioned, and a vinyl group is preferable from the viewpoint of easy synthesis.

【0029】またアルケニル基以外に結合可能な置換又
は非置換の1価の炭化水素基については、上記したとお
りであるが合成の容易さ、組成物の流動性、組成物から
得られる硬化物が良好な物理的性質を保持しうる程度の
重合が可能であることなどからメチル基であることが最
も好ましい。
The substituted or unsubstituted monovalent hydrocarbon group which can be bonded to other than the alkenyl group is as described above, but the ease of synthesis, the fluidity of the composition, and the cured product obtained from the composition are The methyl group is most preferred because it can be polymerized to the extent that good physical properties can be maintained.

【0030】(d)成分のオルガノハイドロジェンシラ
ン又はポリオルガノハイドロジェンシロキサンにおける
ケイ素原子に結合可能な有機機としては、上記の置換又
は非置換の1価の炭化水素基と同様のものをあげること
ができるが、合成の容易さからメチル基が好ましい。
Examples of the organic machine capable of binding to a silicon atom in the organohydrogensilane or polyorganohydrogensiloxane of the component (d) include those similar to the above-mentioned substituted or unsubstituted monovalent hydrocarbon group. However, a methyl group is preferable in terms of ease of synthesis.

【0031】かかる(d)成分としては、ケイ素原子に
結合した水素原子を一分子中に平均2個を超える数を有
するポリオルガノハイドロジェンシロキサンが好まし
い。このポリオルガノハイドロジェンシロキサンとして
は、直鎖状、分岐状、環状等の何れを用いてもよく、ま
たこれらの混合物を用いてもよいが硬化後の組成物自体
に良好な物理的性質を付与するという点で、以下のイ〜
ハで示す化合物又はそれらの混合物を用いることが好ま
しい。
As the component (d), a polyorganohydrogensiloxane having an average of more than 2 hydrogen atoms bonded to silicon atoms in one molecule is preferable. As the polyorganohydrogensiloxane, any of linear, branched, cyclic and the like may be used, and a mixture thereof may be used, but the composition itself after curing has good physical properties. In terms of doing
It is preferable to use the compounds shown by C or a mixture thereof.

【0032】イ.(CH32HSiO1/2とSiO1/2単位
からなり、ケイ素原子に結合した水素原子の含有量が分
子量の0.3〜1.2重量%である分岐状ポリオルガノ
ハイドロジェンシロキサン。
B. A branched polyorganohydrogensiloxane composed of (CH 3 ) 2 HSiO 1/2 and SiO 1/2 units and having a hydrogen atom content bonded to a silicon atom of 0.3 to 1.2% by weight based on the molecular weight.

【0033】ロ.次式: (ただし、pは2〜100、qは0〜100の整数であ
る。)で表され、ケイ素原子に結合した水素原子の含有
量が分子量の0.5〜1.6重量%である直鎖状ポリオ
ルガノハイドロジェンシロキサン。
B. The following formula: (Where p is an integer of 2 to 100 and q is an integer of 0 to 100), and the content of hydrogen atoms bonded to silicon atoms is 0.5 to 1.6 wt% of the molecular weight. Polyorganohydrogen siloxane.

【0034】ハ.次式: (ただし、pは1〜100、qは0〜100の整数であ
る。)で表され、ケイ素原子に結合した水素原子の含有
量が分子量の0.5〜1.6重量%である直鎖状ポリオ
ルガノハイドロジェンシロキサン。
C. The following formula: (However, p is an integer of 1 to 100 and q is an integer of 0 to 100.), and the content of hydrogen atoms bonded to silicon atoms is 0.5 to 1.6% by weight of the molecular weight. Polyorganohydrogen siloxane.

【0035】(d)成分の配合量は、(c)成分中のア
ルケニル基1個に対し、(c)成分中のケイ素原子に結
合した水素原子の数が0.5〜4.0個、好ましくは
1.0〜3.0個となるような量である。水素原子の数
が0.5個未満では組成物の硬化が充分に進行せず、組
成物の硬化物の硬度が低くなり、4.0個を超えると組
成物の硬化物の物理的性質が低下する。
The amount of the component (d) blended is such that the number of hydrogen atoms bonded to silicon atoms in the component (c) is 0.5 to 4.0 with respect to one alkenyl group in the component (c). The amount is preferably 1.0 to 3.0. If the number of hydrogen atoms is less than 0.5, curing of the composition will not proceed sufficiently, and the hardness of the cured product of the composition will be low, and if it exceeds 4.0, the physical properties of the cured product of the composition will be poor. descend.

【0036】一方、付加反応用の硬化触媒としては、
(c)成分のアルケニル基と(d)成分のヒドロシリル
基との間の付加反応を促進するものが用いられ、その例
としては白金系、ロジウム系、パラジウム系の触媒など
があげられる。就中、白金系触媒が好ましく用いられ、
その例としては白金の単体、塩化白金酸、白金−オレフ
ィン錯体、白金−アルコール錯体、白金配位化合物など
をあげることができる。
On the other hand, as a curing catalyst for addition reaction,
A catalyst that promotes the addition reaction between the alkenyl group of the component (c) and the hydrosilyl group of the component (d) is used, and examples thereof include platinum-based, rhodium-based, and palladium-based catalysts. Above all, a platinum-based catalyst is preferably used,
Examples thereof include simple substance of platinum, chloroplatinic acid, platinum-olefin complex, platinum-alcohol complex, platinum coordination compound and the like.

【0037】このような付加反応型の液状混和物の場
合、未架橋液状シリコーンゴムは、硬化剤及び硬化触媒
の存在下、ヒドロシリル化反応が起こり、これが架橋反
応となってゴム状に硬化する。
In the case of such an addition reaction type liquid mixture, the uncrosslinked liquid silicone rubber undergoes a hydrosilylation reaction in the presence of a curing agent and a curing catalyst, and this becomes a crosslinking reaction to cure into a rubber-like state.

【0038】他方、架橋用塗液の調製は、未架橋液状シ
リコーンゴム及び/又はシリコーンオイル、及び硬化剤
と硬化触媒のうち液状混和物に配合しなかった方を混合
することにより行うことができる。架橋用塗液調製用の
未架橋液状シリコーンゴムとしては、液状混和物に準じ
たものを用いることができる。
On the other hand, the cross-linking coating liquid can be prepared by mixing the uncross-linked liquid silicone rubber and / or silicone oil, and the curing agent and the curing catalyst, which have not been added to the liquid mixture. . As the uncrosslinked liquid silicone rubber for preparing the coating liquid for crosslinking, those based on the liquid mixture can be used.

【0039】シリコーンオイルとしては、硬化触媒の存
在下に室温等の低温で硬化剤と反応する官能基を有する
ものや、官能基を有しない液状ポリオルガノシロキサン
などが用いられる。官能基を有しない液状ポリオルガノ
シロキサンからなるシリコーンオイルとしては、トリメ
チルシロキシ基で末端封鎖されたポリジメチルシロキサ
ン又はポリメチルフェニルシロキサンなどが例示され
る。
As the silicone oil, those having a functional group capable of reacting with a curing agent at a low temperature such as room temperature in the presence of a curing catalyst, and liquid polyorganosiloxane having no functional group are used. Examples of the silicone oil composed of a liquid polyorganosiloxane having no functional group include polydimethylsiloxane or polymethylphenylsiloxane end-capped with a trimethylsiloxy group.

【0040】従って架橋用塗液の調製に用いる未架橋液
状シリコーンゴムやシリコーンオイル、硬化剤や硬化触
媒としては、室温等の低温で硬化するように、縮合反応
型や付加反応型等の液状混和物の硬化機構に対応させて
適宜な組合せで選択することができる。
Therefore, as the uncrosslinked liquid silicone rubber or silicone oil, the curing agent or the curing catalyst used in the preparation of the coating liquid for crosslinking, a liquid mixture such as a condensation reaction type or an addition reaction type is mixed so that it can be cured at a low temperature such as room temperature. An appropriate combination can be selected according to the curing mechanism of the product.

【0041】硬化剤の使用量は、未架橋液状シリコーン
ゴム(及び/又はシリコーンオイル)100重量部あた
り0.01〜20重量部、就中0.1〜10重量部が一
般的である。硬化触媒の使用量は、未架橋液状シリコー
ンゴム(及び/又はシリコーンオイル)100重量部あ
たり0.01〜10重量部が一般的である。防食層の表
面の美観を維持する点よりは、表面張力が35dyn/cm
以下の防食層が形成されるようにすることが好ましい。
The amount of the curing agent used is generally 0.01 to 20 parts by weight, especially 0.1 to 10 parts by weight, per 100 parts by weight of the uncrosslinked liquid silicone rubber (and / or silicone oil). The amount of the curing catalyst used is generally 0.01 to 10 parts by weight per 100 parts by weight of the uncrosslinked liquid silicone rubber (and / or silicone oil). The surface tension is 35 dyn / cm from the viewpoint of maintaining the appearance of the anticorrosion layer.
The following anticorrosion layer is preferably formed.

【0042】液状混和物、架橋用塗液の調製に際して
は、例えば充填剤、可塑剤、老化防止剤、防錆剤、防カ
ビ剤、酸化防止剤、紫外線吸収剤、オゾン劣化防止剤、
チキソロープ剤、顔料ないし着色剤などの増粘剤ないし
配合剤を必要に応じて適宜に配合することができる。そ
の配合量は、調製物の1〜90重量%が一般的である。
When preparing the liquid mixture and the coating liquid for crosslinking, for example, a filler, a plasticizer, an antiaging agent, a rust preventive, an antimold agent, an antioxidant, an ultraviolet absorber, an ozone deterioration inhibitor,
Thickeners and compounding agents such as thixotropic agents and pigments and colorants can be appropriately added as needed. The compounding amount thereof is generally 1 to 90% by weight of the preparation.

【0043】調製する液状混和物は、多孔性基材に含浸
させた場合に滴下しない程度の粘度を有するものが好ま
しい。架橋用塗液では、塗布性や室温架橋型被覆材への
浸透性などの点より0.01〜1000ポイズ程度の粘
度(25℃)とすることが好ましい。また架橋用塗液の
施与量を可及的に一定にして均質な防食層を形成する点
よりは、架橋用塗液に顔料ないし着色剤を配合してその
色により施与量を判別できるようにすることが好まし
い。
The liquid mixture to be prepared preferably has a viscosity such that it does not drip when impregnated into a porous substrate. The viscosity of the cross-linking coating liquid is preferably about 0.01 to 1000 poise (25 ° C.) from the viewpoints of coating properties and penetration into the room temperature cross-linking type coating material. Further, from the point of forming a uniform anticorrosion layer by making the applied amount of the crosslinking coating liquid as constant as possible, it is possible to determine the applied amount based on the color of the crosslinking coating liquid by blending a pigment or a coloring agent. It is preferable to do so.

【0044】室温架橋型被覆材は、多孔性基材に液状混
和物を含浸させることにより得ることができる。多孔性
基材は、液状混和物の保持材、室温架橋型被覆材を巻回
又は接着する際の作業時における補助材、防食層の厚さ
の調節材や均一化材、衝撃緩和や損傷防止、光遮断によ
る劣化防止等の防食層保護材などとして機能するもので
ある。従って多孔性基材としては、種々の繊維からなる
例えば織布、不織布、フェルトなどの適宜なものを用い
うる。室温架橋型被覆材は、テープ、シート、切片など
の適宜な形態に形成することができる。
The room temperature crosslinkable coating material can be obtained by impregnating a porous base material with a liquid mixture. The porous base material is a holding material for the liquid mixture, an auxiliary material for the work when winding or adhering the room temperature cross-linking coating material, a material for adjusting the thickness of the anticorrosion layer, a leveling material, impact mitigation and damage prevention. It also functions as a protective material for the anticorrosion layer for preventing deterioration due to light blocking. Therefore, as the porous base material, an appropriate material such as woven cloth, non-woven cloth, and felt made of various fibers can be used. The room temperature cross-linking type covering material can be formed into an appropriate form such as a tape, a sheet, or a section.

【0045】本発明の撥水性防食層の形成は、金属表面
又は防食層欠損部等の防食欠陥部に室温架橋型被覆材を
巻回方式や貼付方式等の適宜な方式で被覆施与し、その
被覆層を架橋用塗液で架橋させることにより行うことが
できる。その架橋は、室温架橋型被覆材と架橋用塗液を
合体させることにより室温等の低温で進行させることが
できる。
To form the water-repellent anticorrosion layer of the present invention, a room temperature cross-linking coating material is applied to a metal surface or an anticorrosion defect portion such as a defect portion of the anticorrosion layer by an appropriate method such as a winding method or an attaching method It can be carried out by crosslinking the coating layer with a crosslinking coating liquid. The crosslinking can be carried out at a low temperature such as room temperature by combining the room temperature crosslinkable coating material and the crosslinking coating liquid.

【0046】従って前記の架橋は、予め架橋用塗液を金
属表面等に塗布しその上に室温架橋型被覆材を施与する
方式、室温架橋型被覆材に架橋用塗液を塗布しそれを金
属表面等に被覆施与する方式、室温架橋型被覆材を金属
表面等に被覆施与しその被覆層に架橋用塗液を塗布する
方式、それらの組合せ方式などの適宜な方式で進行させ
ることができる。表面の平滑性、室温架橋型被覆材の被
覆施与時間の自由性などの点よりは、室温架橋型被覆材
を金属表面等に被覆施与した後に架橋用塗液を塗布する
方式が好ましい。なお架橋に際しては、室温架橋型被覆
材の被覆層をバーナーなどで加熱することにより架橋速
度を速めることができる。
Therefore, the above-mentioned cross-linking is carried out by applying a cross-linking coating solution to a metal surface or the like in advance and then applying a room-temperature cross-linking type coating material thereon. Appropriate methods such as a method of coating on a metal surface, a method of coating a room temperature cross-linking type coating material on a metal surface and the like and applying a cross-linking coating liquid to the coating layer, or a combination thereof. You can From the viewpoints of surface smoothness and freedom of coating application time of the room temperature cross-linking type coating material, it is preferable to coat the room temperature cross-linking type coating material on the metal surface or the like and then apply the cross-linking coating liquid. Upon crosslinking, the crosslinking rate can be increased by heating the coating layer of the room temperature crosslinking type coating material with a burner or the like.

【0047】実施例1 未架橋液状シリコーンゴム100部(重量部、以下同
じ)、ホワイトカーボン(補強剤)100部、テトラエ
トキシシラン(硬化剤)5部をプラネタリーミキサで混
練し、それをポリエステル不織布(目付100g/
2)に含浸させ、それをロール状に巻取って100mm
幅に切断し坪量1kg/m2の室温架橋型被覆材を得た。
Example 1 100 parts of uncrosslinked liquid silicone rubber (parts by weight, the same applies hereinafter), 100 parts of white carbon (reinforcing agent), and 5 parts of tetraethoxysilane (curing agent) were kneaded in a planetary mixer, and the resulting mixture was blended with polyester. Non-woven fabric (Basis weight 100g /
m 2 ), impregnate it into a roll and roll it up to 100 mm
It was cut into widths to obtain a room temperature cross-linking type coating material having a basis weight of 1 kg / m 2 .

【0048】一方、未架橋液状シリコーンゴム100
部、ホワイトカーボン30部、アルミニウム粉(着色
剤)10部、ジブチル錫ジラウレート(硬化触媒)5部
をプラネタリーミキサで混練し、着色型架橋用塗液を得
た。
On the other hand, uncrosslinked liquid silicone rubber 100
Parts, white carbon 30 parts, aluminum powder (colorant) 10 parts, and dibutyltin dilaurate (curing catalyst) 5 parts were kneaded with a planetary mixer to obtain a colored crosslinking coating solution.

【0049】次に、前記の室温架橋型被覆材より長さ1
50mmのサンプルを切取り、それを幅100mm、長さ1
50mm、厚さ2mmの鋼板面に接着し、その上に前記の着
色型架橋用塗液を100g/m2の割合で塗布し、23
℃で24時間保持して室温硬化させ撥水性防食層を形成
した。前記の撥水性防食層に碁盤目状の切れ目を入れ、
JIS K 5400に準拠してテストしたところ評価
点数(10点満点)は10点であった。
Next, the length of the room temperature cross-linking coating material is 1
Cut a sample of 50mm and make it 100mm wide and 1 long
It is adhered to a steel plate surface having a thickness of 50 mm and a thickness of 2 mm, and the coloring type crosslinking coating solution is applied thereon at a rate of 100 g / m 2 , 23
It was kept at ℃ for 24 hours and cured at room temperature to form a water-repellent anticorrosion layer. Make a grid-like cut in the water-repellent anticorrosion layer,
When tested in accordance with JIS K 5400, the evaluation score was 10 (out of 10).

【0050】他方、上記の室温架橋型被覆材を幅50mm
で切断してテープを形成し、それを直径100mmの鋼管
にラップ代55%で巻回したのちその上に上記の着色型
架橋用塗液を100g/m2の割合で塗布し、23℃で
24時間保持して室温硬化させ撥水性防食層を形成し
た。その際、着色型架橋用塗液の塗布後4時間(23
℃)で表面がタックフリーとなり、タックフリー時にお
ける表面張力は27dyn/cm(JIS K 6768)
であった。
On the other hand, the above room temperature cross-linking type covering material is 50 mm wide.
To form a tape, which is wound around a steel pipe having a diameter of 100 mm with a wrap margin of 55%, and then the above-mentioned coloring type crosslinking coating solution is applied at a rate of 100 g / m 2 at 23 ° C. It was kept for 24 hours and cured at room temperature to form a water-repellent anticorrosion layer. At that time, 4 hours (23
The surface becomes tack-free at (° C), and the surface tension when tack-free is 27 dyn / cm (JIS K 6768)
Met.

【0051】前記の撥水性防食層について水密性を評価
したところ良好な結果が得られると共に、鋼管上の撥水
性防食層に切れ目を入れて無理に剥がして重ね合せ部を
観察したところ、重ね合せ部の段差部分も確実に充填さ
れており、水路となる孔部は全く形成されていなかっ
た。
When the water-repellent anticorrosion layer was evaluated for water tightness, good results were obtained, and when the water-repellent anticorrosion layer on the steel pipe was cut and forcibly peeled off, the superposed portion was observed. The stepped portion of the portion was also filled with certainty, and no hole portion to be a water channel was formed.

【0052】実施例2 未架橋液状シリコーンゴム100部、ホワイトカーボン
100部、ジブチル錫ジラウレート5部をプラネタリー
ミキサで混練し、それをポリエステル不織布(目付10
0g/m2)に含浸させ、それをロール状に巻取って1
00mm幅に切断し坪量1kg/m2の室温架橋型被覆材を
得た。
Example 2 100 parts of uncrosslinked liquid silicone rubber, 100 parts of white carbon, and 5 parts of dibutyltin dilaurate were kneaded with a planetary mixer, and the resulting mixture was made into a polyester non-woven fabric (unit weight 10
0 g / m 2 ) and then roll it up to 1
It was cut into a width of 00 mm to obtain a room temperature cross-linking type coating material having a basis weight of 1 kg / m 2 .

【0053】一方、シリコーンオイル100部、ホワイ
トカーボン30部、アルミニウム粉(着色剤)10部、
テトラエトキシシラン5部をプラネタリーミキサで混練
し、着色型架橋用塗液を得た。
On the other hand, 100 parts of silicone oil, 30 parts of white carbon, 10 parts of aluminum powder (colorant),
5 parts of tetraethoxysilane was kneaded with a planetary mixer to obtain a colored crosslinking coating liquid.

【0054】前記の室温架橋型被覆材と着色型架橋用塗
液を用いて実施例1に準じ撥水性防食層を形成しその特
性を調べたところ、碁盤目試験において10点が得られ
ると共に、着色型架橋用塗液の塗布後6時間(23℃)
で表面がタックフリーとなり、タックフリー時における
表面張力は26dyn/cmであった。さらに水密性も良好
で、水路となる孔部は全く形成されていなかった。
A water-repellent anticorrosive layer was formed in accordance with Example 1 using the above-mentioned room temperature crosslinkable coating material and the colored crosslinkable coating liquid, and its characteristics were examined. In addition to obtaining 10 points in the cross-cut test, 6 hours (23 ° C) after the application of the colored crosslinking solution
The surface became tack free, and the surface tension when tack free was 26 dyn / cm. Further, the watertightness was also good, and no pores to be water channels were formed.

【0055】[0055]

【発明の効果】本発明によれば、有機溶剤の関与なく基
材で補強されたシリコーン系の強靱で、撥水性、防食
性、耐熱性、厚さや物性の均一性、密着性に優れる防食
層を作業現場でも簡便に能率よく低温施工で形成するこ
とができる。また形成防食層は、汚染、損傷、シワや浮
きが生じにくく防食効果の長期持続性に優れている。
EFFECTS OF THE INVENTION According to the present invention, an anticorrosion layer which is a silicone-based toughness reinforced by a base material without the involvement of an organic solvent and is excellent in water repellency, corrosion resistance, heat resistance, thickness and physical property uniformity, and adhesion. Can be easily and efficiently formed at a work site by low-temperature construction. In addition, the formed anticorrosion layer is unlikely to cause contamination, damage, wrinkles or floating, and has an excellent long-term anticorrosion effect.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B32B 25/20 F16L 58/10 (72)発明者 三輪 直樹 大阪府茨木市下穂積1丁目1番2号 日東 電工株式会社内 (72)発明者 藤本 哲夫 東京都港区六本木6丁目2番31号 東芝シ リコーン株式会社内 (72)発明者 千葉 修二 東京都港区六本木6丁目2番31号 東芝シ リコーン株式会社内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location B32B 25/20 F16L 58/10 (72) Inventor Naoki Miwa 1-1-1 Shimohozumi, Ibaraki-shi, Osaka No. 2 Nitto Denko Corporation (72) Inventor Tetsuo Fujimoto 6-23-1, Roppongi, Minato-ku, Tokyo Toshiba Silicon Corporation (72) Inventor Shuji Chiba 6-2-131, Roppongi, Minato-ku, Tokyo Toshiba Inside Silicone Co., Ltd.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 未架橋液状シリコーンゴムを主成分とし
硬化剤又は硬化触媒の一方を含有する液状混和物を多孔
性基材に含浸させてなる室温架橋型被覆材を金属表面又
は防食欠陥部に被覆施与して被覆層を形成し、その被覆
層を、未架橋液状シリコーンゴム及び/又はシリコーン
オイルを主成分とし前記の硬化剤又は硬化触媒の他方を
含有する架橋用塗液で架橋させたことを特徴とする撥水
性防食層。
1. A room temperature crosslinkable coating material obtained by impregnating a porous base material with a liquid mixture containing an uncrosslinked liquid silicone rubber as a main component and containing either a curing agent or a curing catalyst on a metal surface or an anticorrosion defect portion. Coating was applied to form a coating layer, and the coating layer was crosslinked with a crosslinking coating liquid containing an uncrosslinked liquid silicone rubber and / or silicone oil as a main component and the other of the above-mentioned curing agent or curing catalyst. A water-repellent anticorrosion layer characterized by the above.
【請求項2】 表面張力が35dyn/cm以下である請求
項1に記載の撥水性防食層。
2. The water-repellent anticorrosion layer according to claim 1, which has a surface tension of 35 dyn / cm or less.
【請求項3】 室温架橋型被覆材からなる被覆層の上に
着色剤を添加した架橋用塗液で架橋してなる着色された
請求項1に記載の撥水性防食層。
3. The water-repellent anticorrosive layer according to claim 1, which is colored by cross-linking with a cross-linking coating liquid in which a colorant is added onto a coating layer made of a room-temperature cross-linking type coating material.
【請求項4】 未架橋液状シリコーンゴムを主成分とし
硬化剤又は硬化触媒の一方を含有する液状混和物を多孔
性基材に含浸させてなる室温架橋型被覆材と、未架橋液
状シリコーンゴム及び/又はシリコーンオイルを主成分
とし前記の硬化剤又は硬化触媒の他方を含有する架橋用
塗液とからなることを特徴とする撥水性防食処理材。
4. A room-temperature cross-linking type coating material obtained by impregnating a porous base material with a liquid mixture containing an uncrosslinked liquid silicone rubber as a main component and containing either a curing agent or a curing catalyst, an uncrosslinked liquid silicone rubber, and And / or a cross-linking coating liquid containing silicone oil as a main component and the other of the above-mentioned curing agents or curing catalysts.
【請求項5】 架橋用塗液が着色剤を含有する請求項4
に記載の撥水性防食処理材。
5. The cross-linking coating liquid contains a colorant.
The water-repellent anticorrosion treatment material according to.
JP07096793A 1993-03-04 1993-03-04 Water repellent anticorrosion layer and anticorrosion treated material Expired - Lifetime JP3172318B2 (en)

Priority Applications (1)

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JP07096793A JP3172318B2 (en) 1993-03-04 1993-03-04 Water repellent anticorrosion layer and anticorrosion treated material

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Application Number Priority Date Filing Date Title
JP07096793A JP3172318B2 (en) 1993-03-04 1993-03-04 Water repellent anticorrosion layer and anticorrosion treated material

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JPH06256975A true JPH06256975A (en) 1994-09-13
JP3172318B2 JP3172318B2 (en) 2001-06-04

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Publication number Priority date Publication date Assignee Title
JPH0899061A (en) * 1994-09-30 1996-04-16 Tonen Corp Formation of silicon oxide-based ceramic film
JPH09238928A (en) * 1996-03-05 1997-09-16 Sekisui Chem Co Ltd Container for blood test
JPH10337804A (en) * 1997-06-09 1998-12-22 Nitto Denko Corp Coating or covering protective structure and protective tape
JP2018130851A (en) * 2017-02-14 2018-08-23 日産自動車株式会社 Transparent film, method for producing transparent film, and antifouling component for automobile
JP2019072856A (en) * 2017-10-12 2019-05-16 日東シンコー株式会社 Protective sheet set
WO2022158035A1 (en) * 2021-01-21 2022-07-28 日東電工株式会社 Anticorrosion tape and anticorrosion structure
WO2023068244A1 (en) * 2021-10-22 2023-04-27 日産化学株式会社 Membrane formation composition, and gas permeation membrane

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0899061A (en) * 1994-09-30 1996-04-16 Tonen Corp Formation of silicon oxide-based ceramic film
JPH09238928A (en) * 1996-03-05 1997-09-16 Sekisui Chem Co Ltd Container for blood test
JPH10337804A (en) * 1997-06-09 1998-12-22 Nitto Denko Corp Coating or covering protective structure and protective tape
JP2018130851A (en) * 2017-02-14 2018-08-23 日産自動車株式会社 Transparent film, method for producing transparent film, and antifouling component for automobile
JP2019072856A (en) * 2017-10-12 2019-05-16 日東シンコー株式会社 Protective sheet set
WO2022158035A1 (en) * 2021-01-21 2022-07-28 日東電工株式会社 Anticorrosion tape and anticorrosion structure
JP2022112340A (en) * 2021-01-21 2022-08-02 日東電工株式会社 Anticorrosive tape and anticorrosive structure
WO2023068244A1 (en) * 2021-10-22 2023-04-27 日産化学株式会社 Membrane formation composition, and gas permeation membrane

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