JPH0577065A - Method for joining steel material for building - Google Patents

Method for joining steel material for building

Info

Publication number
JPH0577065A
JPH0577065A JP23653591A JP23653591A JPH0577065A JP H0577065 A JPH0577065 A JP H0577065A JP 23653591 A JP23653591 A JP 23653591A JP 23653591 A JP23653591 A JP 23653591A JP H0577065 A JPH0577065 A JP H0577065A
Authority
JP
Japan
Prior art keywords
coating
weight
joining
friction
coating material
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
JP23653591A
Other languages
Japanese (ja)
Other versions
JPH08895B2 (en
Inventor
Seiji Tsuchiya
晴史 土屋
Toshio Shinohara
稔雄 篠原
Makoto Emi
真 江見
Hiroyuki Mishima
廣行 三島
Teruyuki Takahashi
輝行 高橋
Makoto Nagamine
誠 長峯
Shigeru Kagayama
繁 加賀山
Tokio Takeyama
時男 竹山
Takeshi Sasaki
健 佐々木
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 KK
Daifuku Co Ltd
Original Assignee
Dai Nippon Toryo KK
Daifuku 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 KK, Daifuku Co Ltd filed Critical Dai Nippon Toryo KK
Priority to JP23653591A priority Critical patent/JPH08895B2/en
Publication of JPH0577065A publication Critical patent/JPH0577065A/en
Publication of JPH08895B2 publication Critical patent/JPH08895B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Pressure Welding/Diffusion-Bonding (AREA)
  • Paints Or Removers (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

PURPOSE:To increase the coefft. of friction to >=0.45 and to allow one coat finishing by previously coating joint surfaces with a specific coating material in the method for joining steel material members by a high strength bolt friction joining method. CONSTITUTION:The organo-alkoxysilane in which the polysiloxane as the constituting component of the coating material consists of 100: 0 to 40 ratios based on the weight of the compd. expressed by general formula RSi(OR')3 and the compd. expressed by R2Si(OR')2 is used in accordance with the conventional method. For example, this organo-alkoxysilane is formed by liberating alcohol by a hydrolysis reaction in an acidic aq. medium and inducing a polycondensation reaction so as to act as a binder. The coefft. of friction of the resulted coating film is maintained at >=0.45. Then, the colloidal silica and colloidal alumina improve the storage stability of the coating material and allow the coating to a larger thickness. A packing material is compounded with this coating material in order to obtain the coating film which is thick and is crackfree.

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、鋼材部材を高力ボルト
摩擦接合法にて接合する方法において、塗装により部材
の接合面に高い摩擦係数を付与した鋼材部材の接合法に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for joining steel members by a high-strength bolt friction joining method, and relates to a method for joining steel members in which a joint surface of the members is provided with a high friction coefficient by painting.

【0002】[0002]

【従来の技術及びその解決すべき課題】建築物は、通
常、鋼材部材を高力ボルト摩擦接合法、リベット接合
法、溶接法等により接合し、構築されているが、特に現
場施工性に優れ、また剛性の高い接合部が得られること
から高力ボルト摩擦接合法が主流を占めている。この高
力ボルト摩擦接合法は、図1にその接合部断面の例を示
すように鋼材部材a、a′を高力ボルト1、ナット2及
びワッシャー3、3′で締め付け、鋼材部材間に生ずる
摩擦力によって応力を伝達する接合法である。従って高
力ボルト摩擦接合面は、通常摩擦係数0.45以上が必要
とされている。
2. Description of the Related Art Buildings are usually constructed by joining steel members by a high strength bolt friction joining method, a rivet joining method, a welding method, etc. The high-strength bolt friction welding method occupies the mainstream because a joint portion having high rigidity can be obtained. In this high-strength bolt friction welding method, steel members a and a'are tightened with high-strength bolts 1, nuts 2 and washers 3 and 3'as shown in FIG. This is a joining method in which stress is transmitted by frictional force. Therefore, the high strength bolt friction joint surface is usually required to have a friction coefficient of 0.45 or more.

【0003】ところで摩擦係数を0.45以上とするため
に、従来鋼材部材の接合面をブラスト処理した後、強制
的に発錆させる方法(イ) 、無機ジンクリッチ塗料を塗装
する方法(ロ) 、亜鉛溶射する方法(ハ) が採用されてい
た。しかしながら前記(イ) の方法では、鋼材部材を接合
し、組立てた後、防錆を目的として全面に通常の防食塗
料を塗装する必要があり、塗装作業性等が悪いという問
題点があった。
By the way, in order to obtain a friction coefficient of 0.45 or more, a method of forcibly rusting after blasting the joint surface of a conventional steel member, and a method of coating an inorganic zinc rich paint (b) The method (c) of spraying zinc was adopted. However, in the method (a), it is necessary to apply a normal anticorrosive paint to the entire surface after joining and assembling the steel members for the purpose of rust prevention, and there is a problem that the workability of painting is poor.

【0004】また前記(ロ) の方法では、通常鋼材部材の
接合面を含め、全面に予め無機ジンクリッチ塗料を塗装
しているが、ジンクリッチ塗膜には白錆が生じ、また仕
上り外観も悪いため、鋼材部材を接合し、組立てた後、
さらに有機系上塗塗料を塗装する必要があり、塗装工程
が増加し、塗装作業性も悪いという問題点があった。な
お、鋼材部材を接合する前に、有機バインダーを使用し
た有機系塗料を接合面に塗装すると、高力ボルト摩擦接
合面の摩擦係数が約0.2前後に低下するため不適当であ
る。
In the method (b), the inorganic zinc-rich paint is usually applied to the entire surface including the joint surface of the steel member in advance. However, the zinc-rich paint film has white rust and has a finished appearance. Because it is bad, after joining the steel members and assembling,
Furthermore, there is a problem that it is necessary to apply an organic topcoat paint, the number of painting processes is increased, and the workability of painting is poor. It is inappropriate to apply an organic paint using an organic binder to the joint surface before joining the steel members, because the friction coefficient of the high strength bolt friction joint surface will drop to about 0.2.

【0005】また前記(ハ) の方法では、溶射膜に白錆が
生じやすく、前記(ロ) の方法と同様の問題点があった。
本発明は、このような現状に鑑み、摩擦係数を0.45以
上にすることが可能で、かつ鋼材部材を接合し、組立て
た後の有機系上塗塗料の塗装が不要な、すなわち1コー
ト仕上げが可能な方法を提供することを目的とする。
Further, the method (c) has the same problem as the method (b) because white rust is likely to occur on the sprayed coating.
In view of such a situation, the present invention makes it possible to set the friction coefficient to 0.45 or more, and does not require the application of the organic top-coat paint after joining and assembling the steel members, that is, a one-coat finish. The purpose is to provide a possible method.

【0006】[0006]

【課題を解決するための手段】本発明者らは鋭意研究の
結果、特定の塗料を接合面に予め塗装することにより上
記目的を達成し得ることを見出し、本発明を完成した。
すなわち、本発明は、建築用鋼材部材を高力ボルト摩擦
接合法により接合する方法において、少なくとも前記部
材の接合面に、予め (a) (i)一般式 RSi(OR′)3 (式中、Rは炭素数1〜8の有機基、R′は炭素数1〜
5の有機基である。)で示される化合物と (ii) 一般式 R2Si(OR′)2 (式中、R、R′は上記定義の通りである)で示される
化合物との(100:0〜40)(重量基準)の割合か
らなるオルガノアルコキシシランを縮合せてめて得られ
た、重量平均分子量500〜50000のポリシロキサ
ン(オルガノアルコキシシラン換算) 10
0重量部、 (b) コロイド状シリカ及び/又はコロイド状アルミナ(固形分換算) 5〜 50重量部 (c) 充填剤 5〜800重量部及び (d) 溶 媒 残 部 からなる塗料を塗布せしめたことを特徴とする、建築用
鋼材部材の接合法からなる。
As a result of earnest research, the present inventors have found that the above object can be achieved by pre-painting a specific coating on the joint surface, and have completed the present invention.
That is, the present invention relates to a method for joining a steel member for construction by a high-strength bolt friction joining method, in which (a) (i) the general formula RSi (OR ') 3 (wherein R is an organic group having 1 to 8 carbon atoms, R'is 1 to 8 carbon atoms
5 is an organic group. ) And a compound of the general formula R 2 Si (OR ′) 2 (wherein R and R ′ are as defined above) (100: 0-40) (weight Polysiloxane having a weight average molecular weight of 500 to 50,000 (calculated as organoalkoxysilane) obtained by condensing organoalkoxysilane having a ratio of (standard).
0 parts by weight, (b) colloidal silica and / or colloidal alumina (as solid content) 5 to 50 parts by weight (c) filler 5 to 800 parts by weight, and (d) coating material consisting of the balance of solvent It is characterized by the joining method of steel members for construction.

【0007】以下本発明を詳細に説明する。本発明にお
いて使用する塗料の構成成分であるポリシロキサンは一
般式RSi(OR′)3で示される化合物とR2Si(OR′)2
で示される化合物との(100:0〜40)(重量基
準)の割合からなるオルガノアルコキシシランを常法に
従って、例えば酸性水性媒体中で加水分解反応によって
アルコールを遊離するとともに重縮合反応を生起し生成
されるものであり、結合剤としての働きをし、また得ら
れる塗膜の摩擦係数を0.45以上に保持するものであ
る。
The present invention will be described in detail below. Polysiloxane which is a component of the paint used in the present invention the general formula RSi (OR ') a compound represented by 3 and R 2 Si (OR') 2
An organoalkoxysilane having a ratio of (100: 0 to 40) (weight basis) with a compound represented by the following formula is used to liberate an alcohol by a hydrolysis reaction in an acidic aqueous medium and to cause a polycondensation reaction. It is formed, acts as a binder, and keeps the friction coefficient of the obtained coating film at 0.45 or more.

【0008】なお、前記一般式中のRは炭素数1〜8の
有機基であり、例えばメチル基、エチル基、n−プロピ
ル基、i−プロピル基などのアルキル基、その他γ−ク
ロロプロピル基、ビニル基、3,3,3−トリフロロプ
ロピル基、γ−グリシドキシプロピル基、γ−メタクリ
ルオキシプロピル基、γ−メルカプトプロピル基、フェ
ニル基、3,4−エポキシシクロヘキシルエチル基、γ
−アミノプロピル基などが代表的なものとして挙げられ
る。
In the above general formula, R is an organic group having 1 to 8 carbon atoms, such as an alkyl group such as a methyl group, an ethyl group, an n-propyl group, an i-propyl group, or a γ-chloropropyl group. , Vinyl group, 3,3,3-trifluoropropyl group, γ-glycidoxypropyl group, γ-methacryloxypropyl group, γ-mercaptopropyl group, phenyl group, 3,4-epoxycyclohexylethyl group, γ
A typical example is an aminopropyl group.

【0009】前記一般式中のR′は炭素数1〜5の有機
基であり、例えばメチル基、エチル基、n−プロピル
基、i−プロピル基、n−ブチル基、sec −ブチル基、
tert−ブチル基、アセチル基などが挙げられる。特に本
発明においてはCH3Si(OR′)3を主成分とするものが好
ましい。またオルガノアルコキシシランは、一般式RSi
(OR′)3で示される化合物単独でもよいが、耐クラッ
ク性、耐厚膜性を向上させるために一般式R2Si(OR′)2
で示される化合物を前記範囲で併用することが出来る。
この範囲よりも過剰になると乾燥性が低下し、また得ら
れる塗膜の硬度が低下し、かつ摩擦係数が0.45より下
るので好ましくない。ポリシロキサン(オルガノアルコ
キシシラン換算)の重量平均分子量は、ポリスチレン換
算重量平均分子量で500〜50000が適当である。
なお、分子量が前記範囲より小さいと得られる塗膜の密
着性が低下し、一方大き過ぎると塗料のゲル化等による
貯蔵安定性が悪くなり、塗膜の密着性も低下するので好
ましくない。
R'in the above general formula is an organic group having 1 to 5 carbon atoms, such as methyl group, ethyl group, n-propyl group, i-propyl group, n-butyl group, sec-butyl group,
Examples thereof include tert-butyl group and acetyl group. Particularly in the present invention, those containing CH 3 Si (OR ′) 3 as a main component are preferable. Further, the organoalkoxysilane has the general formula RSi
The compound represented by (OR ') 3 may be used alone, but in order to improve the crack resistance and thick film resistance, the compound represented by the general formula R 2 Si (OR') 2
The compound shown by can be used together within the above range.
If it exceeds this range, the drying property is lowered, the hardness of the obtained coating film is lowered, and the friction coefficient is lower than 0.45, which is not preferable. The weight average molecular weight of polysiloxane (calculated as organoalkoxysilane) is preferably 500 to 50,000 in terms of polystyrene.
If the molecular weight is smaller than the above range, the adhesiveness of the resulting coating film is deteriorated. On the other hand, if it is too large, the storage stability is deteriorated due to gelation of the paint and the adhesiveness of the coating film is also deteriorated.

【0010】本発明において使用する塗料の構成成分で
あるコロイド状シリカ、コロイド状アルミナは、塗料の
貯蔵安定性を向上させ、厚膜化を可能にし、さらに得ら
れる塗膜の硬度、耐熱性等を向上させるために配合す
る。コロイド状シリカは、無水ケイ酸を親水性有機溶媒
に分散した分散液であり、通常平均粒径約5〜30 m
μ、固形分約10〜40重量%のものであり、含水量4
重量%以下のものが好ましい。市販品としてはオルガノ
シリカゾルIPA−ST、オルガノシリカゾルETC−
ST、オルガノシリカゾル スノーテックス30(以上日
産化学工業社製)、オスカル(触媒化成工業社製)等が
挙げられる。
Colloidal silica and colloidal alumina, which are constituents of the paint used in the present invention, improve the storage stability of the paint and enable thickening, and the hardness and heat resistance of the resulting coating film. To improve the composition. Colloidal silica is a dispersion in which silicic acid anhydride is dispersed in a hydrophilic organic solvent, and usually has an average particle size of about 5 to 30 m.
μ, solid content of about 10 to 40% by weight, water content 4
It is preferably less than or equal to wt%. As commercially available products, organosilica sol IPA-ST, organosilica sol ETC-
ST, organosilica sol Snowtex 30 (all manufactured by Nissan Chemical Industry Co., Ltd.), Oscar (manufactured by Catalysts & Chemicals Industry Co., Ltd.) and the like can be mentioned.

【0011】コロイド状アルミナは、水を溶媒とするpH
2.5〜6のアルミナゾルであり、アルミナ、ベーマイト
などを約5〜25重量%含有し、安定剤として硝酸、塩
酸、酢酸などの酸を使用してなり、通常平均粒径約5〜
200 mμのものである。市販品としてはアルミナゾル
−100、アルミナゾル−200、アルミナゾル−52
0(以上日産化学工業社製)、アルミニウムオキサイド
C(デグサ社製)等が挙げられる。
Colloidal alumina has a pH of water as a solvent.
It is an alumina sol of 2.5 to 6 and contains about 5 to 25% by weight of alumina, boehmite and the like, and an acid such as nitric acid, hydrochloric acid or acetic acid is used as a stabilizer.
It is 200 mμ. As commercial products, alumina sol-100, alumina sol-200, alumina sol-52
0 (above manufactured by Nissan Chemical Industries, Ltd.), aluminum oxide C (manufactured by Degussa) and the like.

【0012】コロイド状シリカ及び/又はコロイド状ア
ルミナの配合量は、固形分換算でポリシロキサン(オル
ガノアルコキシシラン換算)100重量部に対し、5〜
50重量部配合するのが適当である。配合量が前記範囲
より少ないと、塗料の貯蔵安定性が悪くなり、厚膜化が
困難となり、さらに得られる塗膜の硬度が不充分とな
り、しかもクラックが生じやすくなる。一方前記範囲よ
り多過ぎると増粘したり、乾燥性が悪くなったり、さら
にクラックが生じやすくなるのでいずれも好ましくな
い。
The amount of colloidal silica and / or colloidal alumina is 5 to 100 parts by weight of polysiloxane (calculated as organoalkoxysilane) in terms of solid content.
It is suitable to add 50 parts by weight. If the blending amount is less than the above range, the storage stability of the coating composition becomes poor, it becomes difficult to form a thick film, the hardness of the obtained coating film becomes insufficient, and cracks easily occur. On the other hand, when the amount is more than the above range, the viscosity is increased, the drying property is deteriorated, and cracks are more likely to occur.

【0013】本発明において使用する塗料の構成成分で
ある充填剤は、厚膜でクラックの生じない塗膜を得るた
めに配合するものであり、酸化チタン、弁柄、酸化鉄
黄、酸化鉄黒、カーボンブラック、酸化コバルト、酸化
亜鉛等に代表される着色顔料;モリブデン酸亜鉛、縮合
リン酸アルミニウム、リン酸亜鉛、クロム酸カリ、クロ
ム酸亜鉛、代表される防錆顔料;炭酸カルシウム、シリ
カ、ジルコニア、アルミナ、水酸化アルミニウム、ケイ
ソウ土等に代表される体質顔料などの充填剤が代表的な
ものとして挙げられ、これらは1種もしくは2種以上の
混合物として使用される。
The filler, which is a constituent of the paint used in the present invention, is added in order to obtain a thick film free from cracks. Titanium oxide, valve stem, iron oxide yellow, iron oxide black. , Color pigments typified by carbon black, cobalt oxide, zinc oxide, etc .; zinc molybdate, condensed aluminum phosphate, zinc phosphate, potassium chromate, zinc chromate, rust-preventive pigments typified; calcium carbonate, silica, Fillers such as extender pigments typified by zirconia, alumina, aluminum hydroxide, diatomaceous earth and the like can be mentioned as representative ones, and these can be used alone or as a mixture of two or more kinds.

【0014】なお、充填剤の配合量は、ポリシロキサン
(オルガノアルコキシシラン換算)100重量部に対し
5〜800重量部配合するのが適当である。本発明にお
いて使用する塗料の構成成分である溶媒としては、加水
分解反応させるための水及び加水分解される際のゲル化
防止に有効なアルコール類の混合溶媒が好適である。ま
たこれら溶媒はコロイド状シリカ、コロイド状アルミ
ナ、充填剤の分散媒としての役目も果たすものである。
The amount of the filler to be blended is appropriately 5 to 800 parts by weight per 100 parts by weight of polysiloxane (calculated as organoalkoxysilane). As a solvent which is a constituent of the paint used in the present invention, a mixed solvent of water for a hydrolysis reaction and alcohols effective for preventing gelation during hydrolysis is suitable. Further, these solvents also serve as a dispersion medium for colloidal silica, colloidal alumina and filler.

【0015】前記アルコール類としては、メタノール、
エタノール、n−プロピルアルコール、i−プロピルア
ルコール、sec −ブチルアルコール、エチレングリコー
ル、エチレングリコールモノブチルエーテル、酢酸エチ
レングリコールモノエチルエーテル等が代表的なものと
して挙げられる。これら溶媒量は、塗装作業性、前記反
応性等を考慮して、通常塗料の固形分濃度が10〜70
重量%になるよう配合するのが適当である。
The alcohols include methanol,
Representative examples include ethanol, n-propyl alcohol, i-propyl alcohol, sec-butyl alcohol, ethylene glycol, ethylene glycol monobutyl ether, and ethylene glycol monoethyl ether acetate. The amount of these solvents is usually in the range of 10 to 70 in terms of the solid content of the coating in consideration of the coating workability and the reactivity.
It is suitable to mix them in such a manner that the weight% is obtained.

【0016】本発明において使用する塗料は以上説明し
た成分を必須構成成分とし、さらに必要に応じ塗料のpH
を約3〜6にするための無機酸、有機酸、その他界面活
性剤、シランカップリング剤、チタンカップリング剤、
アルカリ金属塩、アミン類、有機錫化合物等の各種添加
剤からなるものである。次に本発明の方法について説明
する。
The paint used in the present invention contains the above-described components as essential constituents, and if necessary, the pH of the paint.
Acid, organic acid, other surfactants, silane coupling agents, titanium coupling agents,
It comprises various additives such as alkali metal salts, amines and organic tin compounds. Next, the method of the present invention will be described.

【0017】本発明でいう建築用鋼材部材は、倉庫、個
人住宅、店舗等の小型建築物に適用される鋼材部材であ
り、高力ボルト摩擦接合法にて接合される前の鋼材部材
の表面を、必要に応じ表面処理、さらに接合部以外の個
所にプライマーを塗装した後、前プラスト処理、酸洗処
理(さらに必要によりリン酸亜鉛処理)等の表面処理、
さらに必要に応じ接合面以外の箇所にプライマーを塗装
した後、前述の塗料を鋼材部材全面に塗装する。塗装個
所は鋼材部材の接合部のみの塗装でもよいが、鋼材部材
を接合し、組立てた後、別途塗装する必要があるので、
鋼材部材を接合する前に接合部も含め全面に塗装するの
が望ましい。
The steel member for construction referred to in the present invention is a steel member applied to small buildings such as warehouses, private houses and shops, and the surface of the steel member before being joined by the high strength bolt friction joining method. Surface treatment, if necessary, and after applying a primer to the parts other than the joint, surface treatment such as pre-plast treatment, pickling treatment (and zinc phosphate treatment if necessary),
Further, if necessary, a primer is applied to a portion other than the joint surface, and then the above-mentioned paint is applied to the entire surface of the steel member. Only the joints of the steel members may be painted, but it is necessary to join the steel members, assemble them, and then paint separately.
Before joining the steel members, it is desirable to coat the entire surface including the joints.

【0018】すなわち本発明で使用する塗料は、ジンク
リッチ塗膜と同様の摩擦係数の高い塗膜が得られ、かつ
ジンクリッチ塗膜の如く白錆発生がなく、また塗膜外観
もよいので、鋼材部材全面に塗装することにより前記1
コート仕上げが可能となり、組立てた後の塗装が省略出
来るのである。鋼材部材への塗装方法としては刷毛塗
装、ローラー塗装、エアスプレー塗装、エアレススプレ
ー塗装、静電スプレー塗装等の通常の方法が採用でき、
常温から300℃の温度で硬化塗膜を形成することが出
来る。塗装は乾燥膜厚で、5〜200μm 、好ましくは
30〜150μm になる程度が適当である。
That is, since the coating material used in the present invention is a coating film having a high friction coefficient similar to that of the zinc-rich coating film, white rust is not generated unlike the zinc-rich coating film, and the coating film has a good appearance. By coating the entire surface of the steel material, the above 1
The coat finish is possible, and the painting after assembling can be omitted. As a coating method for steel members, usual methods such as brush coating, roller coating, air spray coating, airless spray coating and electrostatic spray coating can be adopted.
A cured coating film can be formed at a temperature of room temperature to 300 ° C. The coating is applied to a dry film thickness of 5 to 200 μm, preferably 30 to 150 μm.

【0019】本発明によれば、このようにして摩擦係数
が0.45以上の塗膜を、少なくとも鋼材部材の接合面、
望ましくは全面に施した後、高力ボルト摩擦接合法によ
り鋼材部材を接合し、組立てることができ、建築物が構
築されるのである。
According to the present invention, a coating film having a coefficient of friction of 0.45 or more is thus formed on at least the joint surface of the steel member.
Desirably, after the entire surface is applied, the steel members can be joined and assembled by the high-strength bolt friction joining method to construct a building.

【0020】[0020]

【発明の効果】本発明の方法によれば、鋼材部材を高力
ボルト摩擦接合法にて接合せしめた際の部材の接合面を
摩擦係数0.45以上にすることが可能であり、かつ従来
使用されている無機ジンクリッチ塗料や亜鉛溶射のよう
に白錆が発生せず、また塗膜外観が良く、それ故鋼材部
材を予め接合面だけでなく、全面に塗装しておくと鋼材
部材を接合し、組立てた後、上塗塗装する必要ないの
で、作業工程が短縮出来る。
According to the method of the present invention, when the steel members are joined by the high-strength bolt friction joining method, the joining surface of the members can be made to have a friction coefficient of 0.45 or more. White rust does not occur unlike the used inorganic zinc rich paint and zinc spraying, and the appearance of the coating film is good. Therefore, if the steel members are pre-painted not only on the joint surface but on the entire surface, After joining and assembling, there is no need to apply a top coat, so the work process can be shortened.

【0021】[0021]

【実施例】以下本発明を実施例によりさらに詳細に説明
する。なお実施例中 「部」、 「%」 は重量基準で示
す。塗料用組成物の調製 還流冷却器、攪拌機を備えた反応器内で、メチルトリメ
トキシシラン100 部、イソプロピルアルコール分散コロ
イド状シリカ(固形分20%)100部、水30部及び
イソプロピルアルコール150部を混合し、70℃、2
時間反応させ、重量平均分子量1200のポリシロキサ
ン、コロイド状シリカを含む塗料用組成物(A) を調製し
た。
EXAMPLES The present invention will now be described in more detail with reference to examples. In the examples, "parts" and "%" are shown by weight. Preparation of coating composition In a reactor equipped with a reflux condenser and a stirrer, 100 parts of methyltrimethoxysilane, 100 parts of isopropyl alcohol-dispersed colloidal silica (solid content 20%), 30 parts of water and 150 parts of isopropyl alcohol were added. Mix, 70 ℃, 2
After reacting for a period of time, a coating composition (A) containing a polysiloxane having a weight average molecular weight of 1200 and colloidal silica was prepared.

【0022】前記と同様の操作によりオルガノアルコキ
シシラン、コロイド状シリカ、コロイド状アルミナ、水
及びイソプロピルアルコールを表1に示したように代え
て塗料用組成物(B) 〜 (G)を調製した。
By the same procedure as described above, coating compositions (B) to (G) were prepared by substituting organoalkoxysilane, colloidal silica, colloidal alumina, water and isopropyl alcohol as shown in Table 1.

【0023】[0023]

【表1】 [Table 1]

【0024】注1)「イソプロパノールシリカゾル」
(日産化学工業社製)、固形分20%のイソプロパノー
ル分散液 注2)「アルミナゾル−100」(日産化学工業社
製)、固形分20%の水性分散液 実施例1〜5及び比較例1〜4 表2に示す塗料をショットブラスト処理鋼板(錆グレー
ドSa 2.5、表面粗度平均(Ra) 50μ、最大(Rmax)8
0μ)に、乾燥膜厚50μm になるようにエアースプレ
ー塗装し、150℃、30分間焼付けた。 比較例5〜6 塗料として市販のエポキシ樹脂系塗料(「エポニックス
#20」大日本塗料社製)、無機ジンクリッチ塗料
(「ゼッタールOL」大日本塗料社製)を使用する以外
は実施例1と同様にして塗装し7日間自然乾燥させた。
Note 1) "Isopropanol silica sol"
(Manufactured by Nissan Chemical Industries, Ltd.), isopropanol dispersion liquid with a solid content of 20% Note 2) "Alumina sol-100" (manufactured by Nissan Chemical Industries, Ltd.), aqueous dispersion liquid with a solid content of 20% Examples 1-5 and Comparative Examples 1- 4 The paints shown in Table 2 were shot-blasted steel plates (rust grade Sa 2.5, surface roughness average (Ra) 50μ, maximum (Rmax) 8
0 μ) was air-spray coated to a dry film thickness of 50 μm and baked at 150 ° C. for 30 minutes. Comparative Examples 5 to 6 As Example 1, except that a commercially available epoxy resin-based paint (“Eponics # 20” manufactured by Dainippon Paint Co., Ltd.) and an inorganic zinc-rich paint (“Zettar OL” manufactured by Dainippon Paint Co., Ltd.) were used. It was coated in the same manner and naturally dried for 7 days.

【0025】実施例1〜5及び比較例1〜6で得られた
試験板及び無塗装試験板につき、摩擦係数測定、密着性
試験、塩水噴霧試験(48時間)をし、その結果を表2
の下段に示した。
The test plates and the uncoated test plates obtained in Examples 1 to 5 and Comparative Examples 1 to 6 were subjected to friction coefficient measurement, adhesion test and salt spray test (48 hours), and the results are shown in Table 2.
It is shown in the bottom row.

【0026】[0026]

【表2】 [Table 2]

【0027】表2の試験結果より明らかの通り本発明の
方法により得られた試験板の摩擦係数はいずれも0.45
以上であり、また密着性、耐食性も良好であり、クラッ
ク等のない良好なる塗膜外観を有していた。一方充填剤
を過剰に配合した塗料を使用した比較例1は耐食性、密
着性が不良であった。
As is clear from the test results shown in Table 2, the friction coefficient of the test plate obtained by the method of the present invention is 0.45.
In addition, the adhesiveness and corrosion resistance were good, and the film had a good appearance without cracks. On the other hand, Comparative Example 1 using a coating material containing an excessive amount of filler had poor corrosion resistance and adhesion.

【0028】またオルガノアルコキシシランとして一般
式 Si(OR)4で示されるテトラエトキシシランを多量に
併用した塗料を使用した比較例2、コロイド状シリカも
しくはコロイド状アルミナを配合しない塗料を使用した
比較例4は、いずれも成膜せず、実用的価値ないもので
あった。また一般式R2Si(OR′)2で示されるジメチル
ジメトキシシランを過剰に併用した塗料を使用した比較
例3は、乾燥性不良で、塗膜に粘着性が残り実用的価値
がないものであった。
Comparative Example 2 using a coating material containing a large amount of tetraethoxysilane represented by the general formula Si (OR) 4 as the organoalkoxysilane, and Comparative Example using a coating material containing no colloidal silica or alumina. No. 4 did not form a film and had no practical value. Further, Comparative Example 3 which uses a coating material in which dimethyldimethoxysilane represented by the general formula R 2 Si (OR ′) 2 is used in excess is poor in drying property and sticky to the coating film and has no practical value. there were.

【0029】また有機系塗料を使用した比較例5は摩擦
係数が小さく、高力ボルト摩擦接合法には不適であっ
た。また無機ジンクリッチ塗料を使用した比較例6は摩
擦係数を満足していたが白錆が発生し、上塗塗装を必要
とするものであった。
Further, Comparative Example 5 using the organic paint had a small friction coefficient and was not suitable for the high strength bolt friction welding method. In Comparative Example 6 using the inorganic zinc-rich paint, the coefficient of friction was satisfied, but white rust was generated and top coating was required.

【図面の簡単な説明】[Brief description of drawings]

【図1】図1は高力ボルト摩擦接合部を示す図である。FIG. 1 shows a high strength bolt friction joint.

【符号の説明】[Explanation of symbols]

a、a′ 鋼材部材 1 高力ボルト 2 ナット 3、3′ ワッシャー a, a'Steel material 1 High-strength bolt 2 Nut 3, 3'Washer

───────────────────────────────────────────────────── フロントページの続き (72)発明者 江見 真 大阪府堺市八田北町10−31−1−308 (72)発明者 三島 廣行 京都府長岡京市開田3丁目4−304 ロイ ヤルハイツ藤田 (72)発明者 高橋 輝行 兵庫県芦屋市若葉町2−2−1024 (72)発明者 長峯 誠 滋賀県蒲生郡日野町大字中在寺字上ノ平 1225株式会社ダイフク滋賀製作所内 (72)発明者 加賀山 繁 東京都港区芝2丁目14番5号 株式会社ダ イフク東京本社内 (72)発明者 竹山 時男 東京都港区芝2丁目14番5号 株式会社ダ イフク東京本社内 (72)発明者 佐々木 健 滋賀県蒲生郡日野町大字中在寺字上ノ平 1225株式会社ダイフク滋賀製作所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mami Emi 10-31-1-308 Hattakitamachi, Sakai City, Osaka Prefecture (72) Inventor Hiroyuki Mishima 3-chome, Kaida 3-chome, Nagaokakyo, Kyoto Prefecture Roy Yal Heights Fujita (72) Inventor Teruyuki Takahashi 2-2-1024 Wakaba-cho, Ashiya City, Hyogo Prefecture (72) Inventor Makoto Nagamine 1225 Uenohira, Nakazai-ji, Gino-cho, Gamo-gun, Shiga Prefecture Daifuku Shiga Works, Ltd. (72) Shigeru Kagayama, Tokyo 2-14-5 Shiba, Minato-ku Daifuku Co., Ltd. Tokyo Head Office (72) Inventor Tokio Takeyama 2-14-5 Shiba, Minato-ku Shiba Co., Ltd. Tokyo Head Office (72) Inventor Ken Sasaki Shiga 1225 Kaminohira, Nakazai-ji, Hino-cho, Gamo-gun, Fukushima Prefecture Daifuku Shiga Works

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 鋼材部材を高力ボルト摩擦接合法にて接
合する方法において、少なくとも前記部材の接合面に、
予め (a)(i) 一般式 RSi(OR′)3 (式中、Rは炭素数1〜8の有機基、R′は炭素数1〜
5の有機基である。)で示される化合物と (ii) 一般式 R2Si(OR′)2 (式中、R、R′は上記定義の通りである)で示される
化合物との(100:0〜40)(重量基準)の割合か
らなるオルガノアルコキシシランを縮合せしめて得られ
た、重量平均分子量500〜50000のポリシロキサ
ン(オルガノアルコキシシラン換算)
100重量部、 (b) コロイド状シリカ及び/又はコロイド状アルミナ(固形分換算) 5〜 50重量部 (c) 充填剤 5〜800重量部及び (d) 溶 媒 残 部 からなる塗料を塗布せしめたことを特徴とする、建築用
鋼材部材の接合法。
1. A method for joining steel members by a high-strength bolt friction joining method, wherein at least a joining surface of the members is
In advance, (a) (i) the general formula RSi (OR ′) 3 (wherein R is an organic group having 1 to 8 carbon atoms, R ′ is 1 to 1 carbon atoms).
5 is an organic group. ) And a compound represented by the general formula R 2 Si (OR ′) 2 (wherein R and R ′ are as defined above) (100: 0-40) (weight Polysiloxane having a weight-average molecular weight of 500 to 50,000 (calculated as organoalkoxysilane) obtained by condensing an organoalkoxysilane having a ratio of (standard)
100 parts by weight, (b) colloidal silica and / or colloidal alumina (as solid content) 5 to 50 parts by weight (c) filler 5 to 800 parts by weight, and (d) coating material consisting of the balance of solvent A method for joining steel members for construction, which is characterized in that
JP23653591A 1991-09-17 1991-09-17 Construction steel joining method Expired - Lifetime JPH08895B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23653591A JPH08895B2 (en) 1991-09-17 1991-09-17 Construction steel joining method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23653591A JPH08895B2 (en) 1991-09-17 1991-09-17 Construction steel joining method

Publications (2)

Publication Number Publication Date
JPH0577065A true JPH0577065A (en) 1993-03-30
JPH08895B2 JPH08895B2 (en) 1996-01-10

Family

ID=17002117

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23653591A Expired - Lifetime JPH08895B2 (en) 1991-09-17 1991-09-17 Construction steel joining method

Country Status (1)

Country Link
JP (1) JPH08895B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000145849A (en) * 1998-11-16 2000-05-26 Nsk Warner Kk Wet friction material
JP2010031940A (en) * 2008-07-28 2010-02-12 Takasago Thermal Eng Co Ltd Pipe bracing device
JP2017020009A (en) * 2015-07-08 2017-01-26 シャオドン リュウXiaodong, LIU Inorganic coating composition curable at low temperature and preparation method thereof
FR3130854A1 (en) * 2021-12-21 2023-06-23 Nof Metal Coatings Europe ANTI-CORROSION COATING

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000145849A (en) * 1998-11-16 2000-05-26 Nsk Warner Kk Wet friction material
JP2010031940A (en) * 2008-07-28 2010-02-12 Takasago Thermal Eng Co Ltd Pipe bracing device
JP2017020009A (en) * 2015-07-08 2017-01-26 シャオドン リュウXiaodong, LIU Inorganic coating composition curable at low temperature and preparation method thereof
FR3130854A1 (en) * 2021-12-21 2023-06-23 Nof Metal Coatings Europe ANTI-CORROSION COATING
WO2023118042A1 (en) * 2021-12-21 2023-06-29 Nof Metal Coatings Europe Anti-corrosion coating

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