JPS5815570A - Paint composition for power transmission iron tower - Google Patents

Paint composition for power transmission iron tower

Info

Publication number
JPS5815570A
JPS5815570A JP11353181A JP11353181A JPS5815570A JP S5815570 A JPS5815570 A JP S5815570A JP 11353181 A JP11353181 A JP 11353181A JP 11353181 A JP11353181 A JP 11353181A JP S5815570 A JPS5815570 A JP S5815570A
Authority
JP
Japan
Prior art keywords
weight
power transmission
epoxy resin
parts
composition
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
JP11353181A
Other languages
Japanese (ja)
Other versions
JPS6237065B2 (en
Inventor
Yutaka Ichimura
裕 市村
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.)
Dai Nippon Toryo Co Ltd
Original Assignee
Dai Nippon Toryo 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 Dai Nippon Toryo Co Ltd filed Critical Dai Nippon Toryo Co Ltd
Priority to JP11353181A priority Critical patent/JPS5815570A/en
Publication of JPS5815570A publication Critical patent/JPS5815570A/en
Publication of JPS6237065B2 publication Critical patent/JPS6237065B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To obtain a paint composition for a power transmission iron tower plated with zinc, which paint composition is excellent in the adherence and non- slip characteristics, by making up the composition of an epoxy resin composition, an oxyacid salt or a metal oxide, and a flaky pigment or aggregate. CONSTITUTION:The titled composition consists of 100pts.wt. epoxy resin composition (e.g., a linear or branched bisphenol type epoxy resin) (A) containing two or more epoxy groups at the terminas and one or more hydroxyl groups in the side chain, 1-250pts.wt. compound (B) selected from an oxyacid salt (e.g. zinc phosphate, lead chromate) and a metal oxide (e.g. chrominum trioxide) and 10-500pts.wt. constituent (C) selected from a flaky pigment (e.g. flaky iron oxide, flaky aluminum powder, mica) and an aggregate (e.g. sand, silica sand). If 10-200pts.wt. metal zinc powder and/or calcium plumbate are further added, the long-term adhesion of its coating can further be stabilized and prolonged.

Description

【発明の詳細な説明】 本発明は、亜鉛メッキ、特に溶融亜鉛メッキ被膜を施こ
して成る送電鉄塔、マイクロウェーブ塔などのいわゆる
亜鉛メッキ鉄塔表面の防蝕、着色および滑りIFめのた
めの塗料組成物に係る。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a coating composition for preventing corrosion, coloring, and sliding IF on the surfaces of so-called galvanized steel towers, such as power transmission towers and microwave towers, which are coated with galvanized steel, particularly hot-dip galvanized coatings. Pertaining to things.

従来より、鉄鋼材或いは鉄鋼製品の長期防蝕方法として
、亜鉛メッキが施されており、特に送電鉄塔、マイクロ
ウェーブ塔等を中心とした大型構造物においては溶融亜
鉛メッキ被覆がなされているのは周知のとうりである。
Conventionally, galvanizing has been applied as a long-term corrosion protection method for steel materials and steel products, and it is well known that hot-dip galvanizing is used especially for large structures such as power transmission towers and microwave towers. It is like that.

この防蝕方法は一般の塗料被覆方法に比べるとはるかに
優れるものであるが、最近の如く大気もしくは水質の汚
染の進行に伴なって亜鉛の消耗が著しく、以前のように
は長期の防蝕効果が期待出来なくなっているのが現状で
ある。亜鉛メッキ本来の長期防蝕を効果的ならしめるた
めには、有機塗膜を亜鉛メッキ表面に存在せしめて水、
大気等の腐蝕性因子との接触を防止する事が必要となっ
ており、更には最近の構造物大型化につれて航空標識と
しての必要上或いは環境調和の美観上の観点から構造物
の着色美装の必要性が強く要望されている。
This corrosion prevention method is far superior to general paint coating methods, but as air and water pollution has progressed recently, zinc has been depleted significantly and the long-term corrosion prevention effect is no longer as good as before. The current situation is that we cannot hope for anything. In order to make the long-term corrosion protection inherent in galvanizing effective, an organic coating film must be present on the galvanized surface to prevent water and
It has become necessary to prevent contact with corrosive factors such as the atmosphere, and as structures have become larger in recent years, it has become necessary to color and decorate structures as necessary as aviation signs or from the aesthetic point of view of environmental harmony. There is a strong need for this.

前記の理由により亜鉛メッキ表面への塗装の必要から油
性系塗料或いは合成樹脂系塗料が塗布されているのが現
状である。
For the above-mentioned reasons, oil-based paints or synthetic resin-based paints are currently applied to galvanized surfaces.

しかしこの種の塗料はその塗膜が亜鉛メッキ層の表面か
ら早期に剥離、離脱を生じるという欠点があり必ずしも
満足出来るものではなかった。更に構造物が大型化する
につれて、メンテナンスのための塗替作業に困難を来た
すため長期耐久性、保色性等の点でタールエポキシ樹脂
塗料、タールウレタン樹脂塗料、不飽和ポリエステル樹
脂塗料、或いはエポキシ樹脂エナメル、ポリウレタン樹
脂エナメル等の合成樹脂系塗料の使用が考慮されつつあ
る。
However, this type of paint has the disadvantage that the paint film peels off and separates from the surface of the galvanized layer at an early stage, and is not always satisfactory. Furthermore, as structures become larger, repainting for maintenance becomes difficult, so tar epoxy resin paints, tar urethane resin paints, unsaturated polyester resin paints, or epoxy The use of synthetic resin paints such as resin enamel and polyurethane resin enamel is being considered.

しかし、これらはいずれも密着性が劣るものであった。However, all of these had poor adhesion.

一方、送電鉄塔は保守・点検のために人が昇り降りする
のが普通であるが、従来の塗料組成物から得られた塗膜
は平滑であるため昇降に際し滑り易(、危険を伴うとい
う大きな問題があった。
On the other hand, it is common for people to go up and down power transmission towers for maintenance and inspection purposes, but because the paint films obtained from conventional paint compositions are smooth, they can be easily slippery (and dangerous) when going up and down. There was a problem.

本発明は前記の如き従来塗料のもつ欠点を解消もしくは
改良することを目的とし、亜鉛メッキを施された送電鉄
塔への密着性が優れるとともに、滑り止め性の優れた塗
料組成物を提供しようとするものである。
The present invention aims to eliminate or improve the drawbacks of conventional paints as described above, and seeks to provide a paint composition that has excellent adhesion to galvanized power transmission towers and has excellent anti-slip properties. It is something to do.

即ち、本発明は、 (1) (a)  末端に少な(とも2個以上のエポキ
シ基と側鎖に少なくとも1個以上の水酸基を含有するエ
ポキシ樹脂組成物・・・・・・・・・・・・100重量
部 (b)  酸素酸塩および金属酸化物から選ばれた少な
くとも1種の化合物・・・・・・・・・1〜250重量
部、および (C)  偏平状顔料および骨材から選ばれた少なくと
も1種の成分・・・・・・・・・・・・・・・ 10〜
500重量部から成る送電鉄塔用塗料組成物、および(
2)(a)  末端に少なくとも2個以上のエポキシ基
と側鎖に少なくとも1個以上の水酸基を含有するエポキ
シ樹脂組成物・・・・・・・・・・・・・・・100重
量部 (b)  金属亜鉛粉および/または鉛酸カルシウム・
・・・・・・・・・・・・・・10〜200重量部re
)置部酸素酸塩および金属酸化物から選ばれた少なくと
も1種の化合物・・・・・・・・・1〜150重量部、
および (山 偏平状顔料および骨材から選ばれた少なくとも1
種の成分・・・・・・・・・・・・10〜150重量部 から成る送電鉄塔用塗料組成物に関する。
That is, the present invention provides: (1) (a) An epoxy resin composition containing a small number (both two or more epoxy groups) at the terminal and at least one or more hydroxyl group in the side chain. ...100 parts by weight (b) At least one compound selected from oxyacid salts and metal oxides ...1 to 250 parts by weight, and (C) Oblate pigments and aggregates At least one selected ingredient・・・・・・・・・・・・ 10~
A coating composition for power transmission towers comprising 500 parts by weight, and (
2) (a) Epoxy resin composition containing at least two or more epoxy groups at the terminal end and at least one or more hydroxyl group at the side chain: 100 parts by weight ( b) Metallic zinc powder and/or calcium leadate
・・・・・・・・・・・・・・・10-200 parts by weight re
) At least one type of compound selected from Okipart oxygen acid salts and metal oxides...1 to 150 parts by weight,
and (mountain) at least one selected from flat pigments and aggregates.
The present invention relates to a coating composition for power transmission towers comprising 10 to 150 parts by weight of seed components.

本発明に用いるエポキシ樹脂組成物とは、末端に少なく
とも2個以上のエポキシ基と、分子中に少なくとも1個
以上の水酸基を含有するエポキシ樹脂と、その架橋剤と
の混合物から成るものである。前記エポキシ樹脂として
は例えば直鎖状ビスフェノール型エポキシ樹脂、メチル
置換ビスフェノール型エポキシ樹脂、側鎖状ビスフェノ
ール型エボ牛シ樹脂等がある。市販されている商品名と
しては例えばエピコートにシェル化学@)裂開品名】、
エピクロンに大日本イン午化学工業@)裂開品名】、ア
ラルダイトにチバ・ガイギー@)裂開品名刃などが代表
例として挙げられる。これらは単独使用の池、2種以上
を併用して各々の特徴を出すことも可能である。
The epoxy resin composition used in the present invention consists of a mixture of an epoxy resin containing at least two epoxy groups at the end and at least one hydroxyl group in the molecule, and a crosslinking agent. Examples of the epoxy resins include linear bisphenol type epoxy resins, methyl-substituted bisphenol type epoxy resins, and side chain bisphenol type Ebo-shi resin. Commercially available product names include, for example, Epikote Shell Chemical @) Cleavage product name],
Typical examples include Epicron and Dainippon Ingo Kagaku Kogyo @) Split Product Name] and Araldite and Ciba Geigy @) Split Product Name. These ponds can be used alone, or two or more can be used in combination to bring out the characteristics of each.

本発明の架橋剤としてはエポキシ樹脂分子中に含有され
るエポキシ基もしくは水酸基と相互に反応する基を有す
るもので、一般にエポキシ樹脂用架橋剤として使用され
ているものであればいずれでも良い。例えばジエチレン
トリアミン、トリエチレンテトラミン、メタキシリレン
ジアミン、メタフェニレンジアミン、複素環ジアミンな
どの脂肪族又は芳香挨ポリアミン、ジメチルアミノメチ
ルフェノール、トリス(ジメチルアミノメチル)フェノ
ール、ピペリジンなどの第2級もしくは3級アミン、ポ
リアミド樹脂、アミン付加物(一般にアミンアダクトと
称される)等のアミノ系化合物、トリレンジイソシアネ
ート、ヘキサメチレンジイソシアネート等のイソシアネ
ート化合物の他フェノール樹脂、酸無水物、メラミン樹
脂、尿素樹脂等が挙げられる。本発明の対象が送電鉄塔
という大型構造物であるため常温もしくは強制乾燥程度
でエポキシ樹脂と架橋剤の化学反応が進行するもので、
かつエポキシ基との化学反応を伴なうアミノ系化合物が
最も好ましい。
As the crosslinking agent of the present invention, any crosslinking agent that has a group that reacts with the epoxy group or hydroxyl group contained in the epoxy resin molecule and is generally used as a crosslinking agent for epoxy resins may be used. For example, aliphatic or aromatic polyamines such as diethylenetriamine, triethylenetetramine, metaxylylenediamine, metaphenylenediamine, heterocyclic diamine, secondary or tertiary polyamines such as dimethylaminomethylphenol, tris(dimethylaminomethyl)phenol, piperidine, etc. Amino compounds such as amines, polyamide resins, amine adducts (generally called amine adducts), isocyanate compounds such as tolylene diisocyanate and hexamethylene diisocyanate, as well as phenolic resins, acid anhydrides, melamine resins, urea resins, etc. Can be mentioned. Since the object of the present invention is a large structure such as a power transmission tower, the chemical reaction between the epoxy resin and the crosslinking agent proceeds at room temperature or forced drying.
Most preferred are amino compounds that undergo a chemical reaction with an epoxy group.

本発明の特徴は後述するとうり組成物中に含有される酸
素酸塩および金属酸化物から選ばれた少な(とも1種の
成分が亜鉛メッキ表面と化学的に反応し塗膜の密着性を
附与することにある。とりわけ、リン酸塩を必須成分と
し、リン酸塩以外の他の酸素酸塩、金属酸化物より選ば
れた少なくとも1種以上の成分と併せ用いると、金属イ
オンを介してリン酸とエポキシ樹脂中の水酸基との間に
キレート結合を形成して、強固な密着性を附与する効果
が得られるので好ましい。従って、本発明のエポキシ樹
脂及び架橋剤の混合に際し、架橋剤がエポキシ樹脂分子
中に水酸基との化学反応を伴なう性質のものであれば、
エポキシ樹脂に対する架橋剤の量をエポキシ樹脂1当呈
に対して0.9〜0.5当量程度に調整し、エポキシ樹
脂分子中の水酸基を一部残存せしめておくことが好まし
い。
As will be described later, the feature of the present invention is that a small amount of the oxyacid salt and metal oxide contained in the composition chemically reacts with the galvanized surface and improves the adhesion of the coating film. In particular, when phosphate is used as an essential component and is used in combination with at least one component selected from other oxyacids and metal oxides, This is preferable because a chelate bond is formed between phosphoric acid and the hydroxyl group in the epoxy resin, giving the effect of imparting strong adhesion.Therefore, when mixing the epoxy resin and crosslinking agent of the present invention, the crosslinking agent If it is of a nature that involves a chemical reaction with hydroxyl groups in the epoxy resin molecule,
It is preferable to adjust the amount of the crosslinking agent to the epoxy resin to about 0.9 to 0.5 equivalents per equivalent of the epoxy resin, so that some of the hydroxyl groups in the epoxy resin molecules remain.

本発明に使用する酸素酸塩とは、クロ^酸、リン酸(縮
合リン酸を含む)、ホウ酸、モリブデン酸、燐モリブデ
ン酸、珪モリブデン酸、タングステン酸、燐タングステ
ン酸、珪タングステン酸等の酸素酸と各種金属類とから
成る塩である。
The oxyacid salts used in the present invention include chloroacid, phosphoric acid (including condensed phosphoric acid), boric acid, molybdic acid, phosphomolybdic acid, silicomolybdic acid, tungstic acid, phosphotungstic acid, silicotungstic acid, etc. It is a salt consisting of an oxygen acid and various metals.

例えばストロンチウムクロメート、カルシウムクロメー
ト、クロム酸鉛、ジンククロメート、クロム酸亜鉛、モ
リブデン酸亜鉛、モリブデン酸カルシウム、タングステ
ン酸亜鉛、タングステン酸カルシウム、タングステン酸
マグネシウム、リン酸亜鉛、オルソリン酸鉛、ピロリン
酸鉛、メタリン酸鉛、リン酸アルミニウム、オルソリン
酸部、ピロリン酸部、オキシリン酸部、四ホウ酸亜鉛、
メタホウ酸亜鉛、メタホウ酸鉛、四ホウ酸鉛、メタホウ
酸バリウム等が使用出来る。
For example, strontium chromate, calcium chromate, lead chromate, zinc chromate, zinc chromate, zinc molybdate, calcium molybdate, zinc tungstate, calcium tungstate, magnesium tungstate, zinc phosphate, lead orthophosphate, lead pyrophosphate, Lead metaphosphate, aluminum phosphate, orthophosphate, pyrophosphate, oxyphosphate, zinc tetraborate,
Zinc metaborate, lead metaborate, lead tetraborate, barium metaborate, etc. can be used.

本発明に使用する金属酸化物はクロム、モリブデン、タ
ングステン、マンガン等の酸化物である。
The metal oxides used in the present invention are oxides of chromium, molybdenum, tungsten, manganese, etc.

例えば三酸化クロム、三酸化モリブデン、二酸化タング
ステン、二酸化マンガンなどが使用出来る。これら前記
した酸素酸塩と金属酸化物は、単独使用又は任意の割合
で混合して用いることができる。とりわけ、前記リン酸
塩を必須成分とし、リン酸塩以外の他の酸素酸塩もしく
は金属酸化物から選ばれる少なくとも1種以上の成分と
併用すると、その加水分解により生ずるリン酸が酸素酸
塩もしくは金属酸化物中の金属イオンを介してエポキシ
樹脂中の水酸基との間にキレート化合物を形成すると考
えられるので、その組合せの使用が最も好ましい。
For example, chromium trioxide, molybdenum trioxide, tungsten dioxide, manganese dioxide, etc. can be used. These oxyacid salts and metal oxides described above can be used alone or in a mixture in any proportion. In particular, when the above-mentioned phosphate is used as an essential component and is used in combination with at least one component selected from other oxyacids or metal oxides other than the phosphate, the phosphoric acid produced by its hydrolysis becomes an oxyacid or metal oxide. Since it is thought that a chelate compound is formed between the metal ion in the metal oxide and the hydroxyl group in the epoxy resin, it is most preferable to use that combination.

本発明で使用する前記酸素酸塩および金属酸化物の量は
それら各々の脂粉メッキ表面に対する反応性の強弱、防
蝕性等に大きな差があり、それに応じて変化するが、エ
ポキシ樹脂100重量部に対して次の量で使用する。
The amounts of the oxyacid salts and metal oxides used in the present invention vary depending on their reactivity to the grease powder-plated surface, corrosion resistance, etc., and vary accordingly, but 100 parts by weight of the epoxy resin Use the following amounts for:

即ち、後述する金属亜鉛粉および/または鉛酸カルシウ
ムを併用する場合は、エポキシ樹脂組成物100重量部
に対して1〜150重量部、好ましくは5〜100重量
部であり、又酸素酸塩および金属酸化物から選ばれた少
なくとも1種以上の化合物のみを用いる場合は、エポキ
シ樹脂組成物100重量部に対して1〜250重量部、
好ましくは、10〜120重量;11;の範囲で用いる
That is, when metal zinc powder and/or calcium leadate, which will be described later, are used together, the amount is 1 to 150 parts by weight, preferably 5 to 100 parts by weight, based on 100 parts by weight of the epoxy resin composition. When using only at least one compound selected from metal oxides, 1 to 250 parts by weight per 100 parts by weight of the epoxy resin composition;
Preferably, it is used in a range of 10 to 120 weight; 11;

前記範囲において囮、酸素酸塩、金員酸化物の量が1重
量部より少ないと、亜鉛メッキ表面に対する化成被膜形
成効果あるいはキレート形成効果が期待出来ない。一方
、酸素酸塩、金属酸化物の艦が、150重量部もしくは
250重量部をこえて1使用されると、塗膜の亜鉛メッ
キ面に対する密着性を損なう傾向になる。
If the amount of the decoy, oxyacid salt, or gold member oxide is less than 1 part by weight within the above range, no effect of forming a chemical conversion film or forming a chelate on the galvanized surface can be expected. On the other hand, if more than 150 or 250 parts by weight of the oxyacid or metal oxide is used, the adhesion of the coating film to the galvanized surface tends to be impaired.

本発明に於ては、リン酸塩を必須成分とし、リン酸塩以
外の他の酸素酸塩および金属酸化物より。
In the present invention, phosphate is an essential component, and other oxyacid salts and metal oxides are used.

選ばれた少なくとも1種以上の成分と組み合せて用いる
のが最も効果的であることは前記したとおりであるが、
この場合リン酸塩とリン酸塩以外の他の酸素酸塩および
金属酸化物との好適な混合割合は前者が95〜30重1
にχに後者が5〜70重量%である。
As mentioned above, it is most effective to use it in combination with at least one selected component,
In this case, the preferred mixing ratio of the phosphate and the other oxylate and metal oxide is 95 to 30 parts by weight for the former.
The latter is 5 to 70% by weight.

本発明に使用する偏平状顔料および骨材としては、例え
ば偏平状酸化鉄(Mi caceous I ronO
xide)、偏平状アルミ粉、マイカ、ガラス7ル−ク
、雲母、偏平状鉛粉等の偏平状顔料、砂、砂利、硅砂、
エメIJ−、ガラスピーズ等一般に骨材と称されるもの
が挙げられる。
The flat pigment and aggregate used in the present invention include, for example, flat iron oxide (Mi caceous IronO).
xide), flat aluminum powder, mica, glass 7 luke, mica, flat pigments such as flat lead powder, sand, gravel, silica sand,
Examples include what is generally called aggregate, such as Emme IJ- and glass peas.

これらは1種もしくは2種以上を組合せて使用すること
ができる。
These can be used alone or in combination of two or more.

該偏平状顔料および骨材は、塗膜層の表面に適度な粗度
を附与し、滑り止め効果を大ならしめるものである。
The flat pigment and aggregate impart appropriate roughness to the surface of the coating layer and enhance the anti-slip effect.

前記偏平状顔料および骨材から選ばれた少なくとも1種
の成分は、エポキシ樹++h組成物100重量部に対し
て10〜500重量部、好ましくは50〜300重量部
の範囲で使用する。
At least one component selected from the flat pigment and aggregate is used in an amount of 10 to 500 parts by weight, preferably 50 to 300 parts by weight, based on 100 parts by weight of the epoxy tree++h composition.

上記範囲に於て、その使用量が500ffii部を越え
る場合は、塗膜表面の粗度が大きすぎて、上塗りした際
に発泡する傾向があったり塗膜の付着性が低下し逆に1
0重1部より少ない場合には、塗膜表面への粗度附与効
果がな(、滑り止め効果が全くない。
In the above range, if the amount used exceeds 500 ffii parts, the surface roughness of the coating film will be too large, and there will be a tendency for foaming when overcoating, or the adhesion of the coating film will decrease.
When the weight is less than 1 part by weight, there is no effect of imparting roughness to the surface of the coating film (and there is no anti-slip effect at all).

本発明の別の態様に於ては金属亜鉛粉、鉛酸カルシウム
から選ばれた少なくとも1種以上の成分を用いるが、こ
れら成分は一般に塗料用として使用されているものであ
ればいずれでも良い。該成分のエポキシ樹脂組成物10
0重量部に対する添加量は10〜200重量部、好まし
くは30〜150重量部である。
In another embodiment of the present invention, at least one component selected from metal zinc powder and calcium leadate is used, but any component commonly used for paints may be used. Epoxy resin composition 10 of the components
The amount added to 0 parts by weight is 10 to 200 parts by weight, preferably 30 to 150 parts by weight.

本発明の金属亜鉛粉、鉛酸カルシウムの効果は塗膜の長
期密着性を更に安定、持続せしめるもので、亜鉛メッキ
表面と塗膜の層間にあって緩衝作用により密着性附与の
助成効果を与えるものと考えられる。本発明に於ては鉛
酸カルシウム単独もしくは鉛酸カルシウムと金属亜鉛粉
とを組み合せて用いるのが密着性の持続効果が大きい。
The effect of the metal zinc powder and calcium leadate of the present invention is to further stabilize and sustain the long-term adhesion of the coating film, and it is located between the galvanized surface and the coating film, and has a buffering effect to promote adhesion. considered to be a thing. In the present invention, the use of calcium leadate alone or in combination with calcium leadate and metal zinc powder has a great effect on maintaining adhesion.

2種を組み合わせて用いる際の鉛酸カルシウムと金属亜
鉛粉との混合割合は前者が80〜40重i%に後者が2
0〜60重量%が最も効果的である。本発明の金属亜鉛
粉、鉛酸カルシウムから選ばれた少なくとも1種以上の
成分が10重量部より少ないと塗膜密着の持続効果がな
く、200重量部より多くなると密着性を損なう傾向に
ある。
When using the two types in combination, the mixing ratio of calcium leadate and metal zinc powder is 80 to 40% by weight for the former and 2% for the latter.
0-60% by weight is most effective. If the amount of at least one component selected from the metal zinc powder and calcium leadate of the present invention is less than 10 parts by weight, there is no sustained effect on coating adhesion, and if it is more than 200 parts by weight, the adhesion tends to be impaired.

本発明は前記した如く、エポキシ樹脂組成物と金属亜鉛
粉、鉛酸カルシウムから選ばれた少なくとも1種の成分
、酸素酸塩、金属酸化物から選ばれた少なくとも1種の
化合物、及び偏平状顔料および骨材から選ばれた少なく
とも1種の成分を各々前記量比で存在せしめた組成物を
使用することにより、亜鉛メッキ被膜表面に対して強固
な密着性を有し、しかもその効果が長期にわたって持続
する塗膜を得ることが出来、かつ偏平状顔料および/ま
たは骨材により、亜鉛メッキ被膜表面に対して強固な密
着性を附与するとともに滑り止め効果を附与するもので
ある。
As described above, the present invention comprises an epoxy resin composition, metallic zinc powder, at least one component selected from calcium leadate, at least one compound selected from oxyacid salts, metal oxides, and a flat pigment. By using a composition in which at least one component selected from aggregate and aggregate is present in the above-mentioned ratio, it has strong adhesion to the surface of the galvanized coating and has a long-lasting effect. A long-lasting coating film can be obtained, and the flat pigment and/or aggregate provide strong adhesion to the surface of the galvanized coating and provide an anti-slip effect.

本発明に於ては、前記の必須成分の他に、前記組成物と
相溶性のあるその他の樹脂を本発明の目的を損わない範
囲で添加することも可能である。
In the present invention, in addition to the above-mentioned essential components, it is also possible to add other resins that are compatible with the above-mentioned composition within a range that does not impair the object of the present invention.

更に所望によりその他の防錆顔料、タルク、シリカ等の
体質顔料、酸化鉄、カーボンブラック、酸化チタン等の
着色顔料、アスファルト、タール、ピッチ等の歴青質、
沈澱防止剤、ダレ防止剤、界面活性剤、表面調整剤等の
添加剤、塗膜の付着力を一層助成するためのカップリン
グ剤、キレート化合物或いは溶媒等を添加することがで
きる。
Furthermore, if desired, other anti-rust pigments, extender pigments such as talc and silica, coloring pigments such as iron oxide, carbon black and titanium oxide, bituminous substances such as asphalt, tar and pitch,
Additives such as anti-settling agents, anti-sag agents, surfactants, surface conditioners, coupling agents, chelate compounds, solvents, etc. to further enhance the adhesion of the coating can be added.

尚、本発明に於て溶媒として水板外の有機溶媒系を使用
する場合1こは組成物中の酸素酸塩、金属酸化物の金属
イオンの溶出もしくは加水分解を助成するため少なくと
も1種以上のアルコール系溶媒もしくは溶媒に対し3重
量%以下程度の水を組成物中に含有して成ることが好ま
しい。
In addition, in the case where an organic solvent system other than water is used as a solvent in the present invention, at least one type of organic solvent is used to assist the elution or hydrolysis of metal ions of oxyacid salts and metal oxides in the composition. It is preferable that the composition contains about 3% by weight or less of water based on the alcoholic solvent or solvent.

本発明の前記成分から成る塗料組成物は亜鉛メッキ表面
に刷毛、スプレー、ローラー、ヘラ、コテ等の公知方法
により、10〜1000ミクロン程度の乾燥膜厚が得ら
れる様に調整して塗布し、エポキシ樹脂と架橋剤が化学
反応を呈し、塗膜乾燥するに必要な条件下で塗膜硬化を
せしめること(こより、前記効果を有する塗膜を得るこ
とができる。
The coating composition comprising the above-mentioned components of the present invention is applied to a galvanized surface by a known method such as a brush, spray, roller, spatula, trowel, etc. to obtain a dry film thickness of about 10 to 1000 microns, The epoxy resin and the crosslinking agent exhibit a chemical reaction, and the coating film is cured under the conditions necessary for drying the coating film (this makes it possible to obtain a coating film having the above-mentioned effects).

しかして、鉄塔の用途、目的などに応じて、例えばポリ
ウレタン樹脂塗料、エポキシ樹脂塗料、塩化ゴム系塗料
、塩化ビニル樹脂塗料等各色任意の塗料を本発明の滑り
止め効果を失しない程度の厚みに上塗りすること、およ
びエポキシ樹脂系あるいはポリウレタンtkl B”a
系プライマーをあらかじめ塗布した上に本発明の組成物
を塗布することなどが可能である。
Depending on the use and purpose of the steel tower, paints of various colors such as polyurethane resin paint, epoxy resin paint, chlorinated rubber paint, vinyl chloride resin paint, etc. can be applied to a thickness that does not lose the anti-slip effect of the present invention. Overcoating and epoxy resin-based or polyurethane tkl B”a
It is possible to apply the composition of the present invention after previously applying a primer.

本発明の塗料組成物から得られた塗膜は長期の曝露に対
して強い耐久性を示すもので、従来の如く短期間で剥離
、離脱することなく長期に安定した密着性を有するとと
もに優れた滑り止め効果を有するものである。
The coating film obtained from the coating composition of the present invention exhibits strong durability against long-term exposure, and has stable adhesion over a long period of time without peeling or falling off in a short period of time as in the case of conventional coatings. It has an anti-slip effect.

次に本発明の具体的効果を実施例により示す。Next, specific effects of the present invention will be shown by examples.

尚、実施例及び比較例の「部」又は「%」は「重量部」
又は「重量%」を意味する。
In addition, "parts" or "%" in Examples and Comparative Examples are "parts by weight"
Or it means "% by weight".

実施例1゜ エポキシ当量450〜500の直鎖状ビスフェノール型
エポキシ樹脂と架橋剤として活性水素当量150のポリ
アミド樹脂を用いて、エポキシ樹脂と架橋剤をエポキシ
樹脂1当量に架橋剤0.8当量の割合で混合し本発明に
使用するエポキシ樹脂組成物を得た。その他の成分につ
いては表−1に示した割合で混合した。尚比較のための
本発明外の組成物(比較試料Nα1〜4)も同様にして
得た。
Example 1゜Using a linear bisphenol type epoxy resin with an epoxy equivalent of 450 to 500 and a polyamide resin with an active hydrogen equivalent of 150 as a crosslinking agent, the epoxy resin and crosslinking agent were added to 1 equivalent of the epoxy resin and 0.8 equivalent of the crosslinking agent. The epoxy resin composition used in the present invention was obtained by mixing in the following proportions. Other components were mixed in the proportions shown in Table-1. Compositions other than the present invention (comparative samples Nα1 to Nα4) for comparison were also obtained in the same manner.

次いで、必要に応じてキシレン:n−ブチルアルコール
=1:1(重量比)からなる混合溶剤を用いて塗装作業
に適する粘度に調整し、溶融亜鉛メッキ表面に乾燥膜厚
200ミクロンとなるように塗装し、20℃、75%R
Hの条件下で7日間乾燥せしめて、初期密着性、屋外曝
露および滑り止め試験に供した。
Next, if necessary, use a mixed solvent consisting of xylene:n-butyl alcohol = 1:1 (weight ratio) to adjust the viscosity to a suitable level for painting work, so that the dry film thickness is 200 microns on the hot-dip galvanized surface. Painted, 20℃, 75%R
After drying under H conditions for 7 days, it was subjected to initial adhesion, outdoor exposure, and anti-slip tests.

=19一 実施例え エポキシ当量900〜1000の直鎮ビスフェノール型
エポキシ樹脂と架橋剤として活性水素当量200のアミ
ンアダクトを用いてエポキシ樹脂と架橋剤を当量で混合
し、エポキシ樹脂組成物を得た。
=19 Example 1 Using a direct-setting bisphenol type epoxy resin having an epoxy equivalent of 900 to 1000 and an amine adduct having an active hydrogen equivalent of 200 as a crosslinking agent, the epoxy resin and the crosslinking agent were mixed in equivalent amounts to obtain an epoxy resin composition.

尚比較のための本発明外の組成物(比較試料ib 5〜
7)も同様にして得た。表−2の組成より成る塗料組成
物を調整し、溶融亜鉛メッキ鋼板の表面に乾燥膜厚が1
50ミクロンとなるように塗装し、20℃、75546
RHの条件下で7日間乾燥せしめて比較試験に供した。
Compositions other than the present invention for comparison (comparative samples ib 5 to
7) was obtained in the same manner. A coating composition having the composition shown in Table 2 was prepared, and a dry film thickness of 1 was applied to the surface of a hot-dip galvanized steel sheet.
Painted to a thickness of 50 microns, 20℃, 75546
It was dried under RH conditions for 7 days and subjected to a comparative test.

尚、実施例2の各塗料塗装に際しキシレン:n−ブチル
アルコール=1:1(重量比)の混合溶剤で適性粘度に
調整した。
In addition, when applying each paint in Example 2, the viscosity was adjusted to an appropriate level using a mixed solvent of xylene:n-butyl alcohol=1:1 (weight ratio).

−21− 比較実験1 前記の如くして得られた本発明試料Nα1〜11と比較
試料1〜7の供試片を用い、初期の亜鉛メッキ表面に対
する塗膜の密着性を試験するため、カッターナイフを用
いて塗膜に幅3 tri間隔で亜鉛メッキ表面に達する
タテ11本、ヨコ11本の直角にクロスする切線を入れ
100個のマス目を形成せしめる。次いで該マス目箇所
にセロハンテープを圧着し瞬時にセロハンテープを引剥
し、マス目の残存数を百分率として表わす。
-21- Comparative Experiment 1 Using the specimens of the present invention samples Nα1 to 11 and comparative samples 1 to 7 obtained as described above, a cutter was used to test the adhesion of the coating film to the initial galvanized surface. Using a knife, make 11 vertical and 11 horizontal cutting lines that cross at right angles to the galvanized surface at intervals of 3 tri in width to form 100 squares. Next, cellophane tape is pressed onto the squares, the cellophane tape is instantly peeled off, and the number of remaining squares is expressed as a percentage.

一方、他の供試片を用いて供試体中央部で斜めにクロス
する炬鉛メッキ表面に達する2本の切線を入れ、3ケ年
間の屋外曝露に供した。3ケ年間経過後、塗膜表面を観
察して塗膜欠陥、異状発生の有無を確認したのちに同−
供試片の残存塗膜に対して前記初期密着性試験と同一手
順の処理、判定方法により、長期曝露後の密着性良否を
判定する。各々得られた結果を表−3に示した。
On the other hand, using another test piece, two cutting lines reaching the lead plating surface were cut diagonally across the center of the test piece, and the test piece was subjected to outdoor exposure for three years. After 3 years, the surface of the paint film was observed to confirm the presence or absence of paint film defects and abnormalities.
The adhesion quality after long-term exposure is determined for the residual coating film of the test piece using the same procedure and determination method as in the initial adhesion test. The results obtained are shown in Table 3.

表−3比較試験結果表 比較実験2゜ 前記の如くして得られた本発明の試料Nα1〜11、と
比較試料Nα1〜7の供試庁を用い、0.5X5X5?
形状のフック付ゴム板を供試片表面にのせ、更にゴム板
表面にIKfの重りをのせる。ゴム板のフックにバネ秤
を取付け、供試片と水平の方向に、バネ秤を引張り、ゴ
ム板が移動し始めた時の力をKg/25artとしてバ
ネ秤の目盛より読みとる。各々得られた結果を表−4に
示した。
Table 3 Comparative Test Results Table Comparative Experiment 2゜ Using the samples Nα1 to 11 of the present invention obtained as described above and the test samples of comparative samples Nα1 to 7, 0.5X5X5?
A rubber plate with a hook of the same shape is placed on the surface of the specimen, and a weight of IKf is placed on the surface of the rubber plate. Attach a spring scale to the hook of the rubber plate, pull the spring scale in a direction parallel to the specimen, and read the force when the rubber plate starts to move as Kg/25 art from the scale of the spring scale. The results obtained are shown in Table 4.

表−4 前記比較実験結果表より明らかに、本発明の塗料組成物
より得られた塗膜層は、亜鉛メッキ表面に対する密着性
付与効果は非常に優れたものである。従って、塗膜の防
蝕効果、長期付着性が優れるため、亜鉛メッキ表面を長
期間にわたって保護することが可能なのである。加えて
滑り止め効果にも優れているため、保守、点検のための
鉄塔昇降に際しても、安全確保の点で極めて有効なもの
である。
Table 4 It is clear from the comparative experiment results table that the coating layer obtained from the coating composition of the present invention has an extremely excellent adhesion effect to the galvanized surface. Therefore, the corrosion-proofing effect and long-term adhesion of the coating film are excellent, making it possible to protect the galvanized surface for a long period of time. In addition, it has an excellent anti-slip effect, making it extremely effective in ensuring safety when going up and down steel towers for maintenance and inspection.

出願人二大日本塗料株式会社Applicant Nidai Nippon Toyo Co., Ltd.

Claims (1)

【特許請求の範囲】 (1)(a)末端に少なくとも2個以上のエポキシ基と
側鎖に少なくとも1個以上の水酸基を含有するエポキシ
樹脂組成物・・・・・・100重量部(b)  酸素酸
塩および金属酸化物から選ばれた少なくとも1種の化合
物 1〜250重量部および (C)、偏平状顔料および骨材から選ばれた少な(とも
1種の成分 ・・・・・・10〜500重]・部 から成る送電鉄塔用塗料組成物。 (2)前記酸素酸塩および金属酸化物から選ばれた少な
くとも1種の化合物1す、リン酸塩を必須成分とし、リ
ン酸塩以外の他の酸素酸塩および金属酸化物より選ばれ
た少なくとも1挿具」二の成分である特許請求の範囲第
(1)項記載の送電鉄塔用塗料組成物。 (3)前記偏平状顔料および骨材から選ばれた少な(と
も1種の成分は、偏平状酸化鉄である特許請求の範囲第
(1)項記載の送電鉄塔用塗料組成物。 (41(al末端に少なくとも2個以上のエポキシ基と
側鎖に少なくと も1個以上の水酸基を含有す るエポキシ樹脂組(物・・・・・・・・・・・・100
重量部。 (b)金属亜鉛粉および/または鉛 酸カルシウム・・・・・・・・・10〜200重量部。 (C)酸素酸塩および金属酸化物か ら選ばれた少なくとも1種の 化合物・・・・・・・・・・・・・・・・・・・・・・
・・1〜150重量部、および(dl偏平状顔料および
骨材から 選ばれた少なくとも1種の Ji会・・・・・・−・・・・−・・−・・・・−・・
・・・・・10〜500重量部から成る送電鉄塔用塗料
組成物。 (5)前記(b)成分が鉛酸カルシウムである特許請求
の範囲第(4)項記載の送電鉄塔用塗料組成物。 (6)前記(b)成分が金属亜鉛粉と鉛酸カルシウムの
混合物である特許請求の範囲第(4)項記載の送電鉄塔
用塗料組成物。 (7)前記酸素酸塩および金属酸化物から選ばれた少な
くとも1種の化合物1よ、リン酸塩を必須成分とし、リ
ン酸塩以外の他の酸素酸塩および金属酸化物より選ばれ
た少なくとも1種以上の成分である特許請求の範囲第(
4)項記載の送電鉄塔用塗料組成物。 (8)前記偏平状顔料および骨材から選ばれた少な(と
も1種の成分は偏平状酸化鉄である特許請求の範囲第(
4)項記載の送電鉄塔用塗料組成物。
[Claims] (1) (a) Epoxy resin composition containing at least two or more epoxy groups at the end and at least one or more hydroxyl group at the side chain...100 parts by weight (b) 1 to 250 parts by weight of at least one compound selected from oxyacid salts and metal oxides; ~500 parts by weight]. (2) At least one compound selected from the above-mentioned oxyacids and metal oxides, containing phosphate as an essential component and other than phosphate. The coating composition for power transmission towers according to claim (1), which comprises at least one component selected from other oxyacids and metal oxides. (3) The flat pigment and The coating composition for power transmission towers according to claim (1), wherein at least one component selected from the aggregate is flat iron oxide. Epoxy resin set (product) containing an epoxy group and at least one hydroxyl group in the side chain
Weight part. (b) Metallic zinc powder and/or calcium leadate...10 to 200 parts by weight. (C) At least one compound selected from oxyacid salts and metal oxides...
...1 to 150 parts by weight, and at least one Ji group selected from (dl flat pigments and aggregates)...
...A coating composition for power transmission towers comprising 10 to 500 parts by weight. (5) The coating composition for power transmission towers according to claim (4), wherein the component (b) is calcium leadate. (6) The coating composition for power transmission towers according to claim (4), wherein the component (b) is a mixture of metal zinc powder and calcium leadate. (7) At least one compound 1 selected from the above-mentioned oxysaccharides and metal oxides, which has a phosphate as an essential component, and at least one selected from other oxysaccharides other than phosphates and metal oxides. Claim No. 1, which is one or more components (
The coating composition for power transmission towers according to item 4). (8) A component selected from the flat pigment and the aggregate is flat iron oxide.
The coating composition for power transmission towers according to item 4).
JP11353181A 1981-07-22 1981-07-22 Paint composition for power transmission iron tower Granted JPS5815570A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11353181A JPS5815570A (en) 1981-07-22 1981-07-22 Paint composition for power transmission iron tower

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11353181A JPS5815570A (en) 1981-07-22 1981-07-22 Paint composition for power transmission iron tower

Publications (2)

Publication Number Publication Date
JPS5815570A true JPS5815570A (en) 1983-01-28
JPS6237065B2 JPS6237065B2 (en) 1987-08-11

Family

ID=14614679

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11353181A Granted JPS5815570A (en) 1981-07-22 1981-07-22 Paint composition for power transmission iron tower

Country Status (1)

Country Link
JP (1) JPS5815570A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5813670A (en) * 1981-07-17 1983-01-26 Dainippon Toryo Co Ltd Treating method of galvanized film surface
JPS5845906A (en) * 1981-09-14 1983-03-17 松下電工株式会社 Manufacture of decorative veneer

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5813670A (en) * 1981-07-17 1983-01-26 Dainippon Toryo Co Ltd Treating method of galvanized film surface
JPS5845906A (en) * 1981-09-14 1983-03-17 松下電工株式会社 Manufacture of decorative veneer

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60173587U (en) * 1984-04-25 1985-11-16 飯田 星祥 ▲Pulling machine
JPS6152687U (en) * 1984-09-12 1986-04-09
JPS6175489U (en) * 1984-10-23 1986-05-21
JPS62260866A (en) * 1986-05-07 1987-11-13 Shinto Paint Co Ltd Method of treating surface of weatherable steel to stabilize rust
US5624978A (en) * 1987-05-11 1997-04-29 Morton International, Inc. Conductive, internally lubricated barrier coating for metal
KR100384247B1 (en) * 2000-09-26 2003-05-14 조달형 Zinc-coated low carbon steel wires
JP2006169332A (en) * 2004-12-15 2006-06-29 Nissan Motor Co Ltd Colored top coating composition and colored top coating film
US7348061B2 (en) * 2005-01-07 2008-03-25 The Sherwin-Williams Company Slip-resistant coatings and substrates coated therewith
JP2014148613A (en) * 2013-02-01 2014-08-21 Dainippon Toryo Co Ltd Zinc powder-containing coating composition

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