JPS6362546B2 - - Google Patents

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Publication number
JPS6362546B2
JPS6362546B2 JP58216948A JP21694883A JPS6362546B2 JP S6362546 B2 JPS6362546 B2 JP S6362546B2 JP 58216948 A JP58216948 A JP 58216948A JP 21694883 A JP21694883 A JP 21694883A JP S6362546 B2 JPS6362546 B2 JP S6362546B2
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JP
Japan
Prior art keywords
parts
weight
powder
metal
rust preventive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP58216948A
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Japanese (ja)
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JPS60108445A (en
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Priority to JP58216948A priority Critical patent/JPS60108445A/en
Publication of JPS60108445A publication Critical patent/JPS60108445A/en
Publication of JPS6362546B2 publication Critical patent/JPS6362546B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

本発明はり゚ルダブルホツトメルト防錆剀組成
物、曎に詳しくは点溶接重ね合せ面の防錆に䜿甚
する組成物に関し、その目的ずする所は、防錆
力、点溶接性に優れ、䞔぀塗膜の密着性、物理的
匷床、耐氎性及び耐湿性の良奜なり゚ルダブルホ
ツトメルト防錆剀組成物を提䟛せんずするにあ
る。 埓来、点溶接は非垞に簡䟿で、胜率的な金属板
の接合方法であるために、殆んどの金属加工業で
広く䜿甚されおいるが、点溶接䜜業性、溶接匷床
等のために、金属は未凊理の、裞のたた行なわれ
おいるのが倧郚分である。その結果、点溶接重ね
合せ面は、さびが発生し易く、又溶接埌は完党な
防錆凊理が䞍可胜であるために、防錆力及び溶接
性に優れた点溶接重ね合せ面甚防錆剀の開発が長
幎来の倧きな課題にな぀おいる。 珟圚、業界の䞀郚でゞンクリツチペむントが点
溶接重ね合せ面の防錆に䜿甚されおいるが、溶剀
型塗料であるために、有機溶剀による火灜の危険
性䞊びに人䜓に察する衛生䞊の問題があり、広く
普及するたでには至぀おいない。 たたクロム酞ず亜鉛末などを含む薬液を塗垃し
焌付けた鋌板の䞊に゚ポキシ暹脂系ゞンクリツチ
ペむントを焌付けたコヌト系のゞンクロメタル
凊方が、薄膜で防錆力にすぐれ、スポツト溶接性
が良奜であるために、スポツト溶接可胜な防錆凊
理法ずしお䜿甚されおいるが、塗装工皋が工皋
である䞊に焌付枩床が非垞に高くお䜜業性に劣る
のず、ゞンクリツチペむントの有機溶剀のほか、
クロム酞の毒性の問題があり、点溶接重ね合せ面
甚防錆剀ずしおは殆んど䜿甚されおいない。 本発明者は䞊蚘埓来品の難点に泚目し、有機溶
剀䜿甚に基づく難点がなく、䜜業性が良奜工
皋でなく工皋で可胜なで、しかもり゚ルダブ
ル防錆剀ずしお芁求される芁件たずえば防錆剀及
び溶接性が良奜で、塗膜の密着性、耐氎性、耐湿
性に優れた防錆剀を開発すべく研究を続けた結
果、本発明を完成したものであ぀お、即ち本発明
は (a) 酞化ペトロラタム、酞化ワツクス、これらの
金属塩又ぱステル、ラノリン金属塩、及び石
油スルホン酞又は合成スルホン酞の金属塩の少
なくずも皮、20〜80重量郚、ペトロラタム、
ラノリン及びワツクスの少なくずも皮、20〜
80重量郚よりなる混合物、10〜90重量郚、 (b) ポリ゚チレン、ポリプロピレン、゚チレン・
アクリル酞共重合䜓、゚チレン・゚チルアクリ
レヌト共重合䜓、゚チレン・酢酞ビニル共重合
䜓の少なくずも皮、10〜90重量郚、及び(a)ず
(b)の和100重量郚に察しお、 (c) 䜓積抵抗30Ω・cm以䞋の導電性充填材、10〜
300重量郹 を含有しおなるこずを特城ずするり゚ルダブルホ
ツトメルト防錆剀組成物に係るものである。 本発明においお䜿甚する(a)成分の酞化ペトロラ
タム、酞化ワツクス、これらの金属塩又ぱステ
ル、ラノリン金属塩、石油スルホン酞又は合成ス
ルホン酞の金属塩、ペトロラタム、ラノリン、ワ
ツクスずしおは䞀般のワツクス系防錆塗料に埓来
から䜿甚されお来たものが広い範囲で䜿甚出来、
就䞭軟化点40〜180℃皋床のものが奜たしく䜿甚
出来る。 たた、䞊蚘各成分の内の各金属塩の金属ずしお
は、特に限定されるこずなく、倚くの金属が䜿甚
でき、䟋えばナトリりム、カリりム、リチりム等
のアルカリ金属、カルシりム、バリりム、ストロ
ンチりム等のアルカリ土類金属、モリブデン、亜
鉛等を挙げるこずができる。これらの内、アルカ
リ金属及びアルカリ土類金属が、防錆効果の点か
ら奜たしい。これらの金属塩の金属は、皮であ
぀おもよいし、皮以䞊であ぀぀おも勿論差し぀
かえない。 (b)成分のポリ゚チレンは、高密床ポリ゚チレン
及び䜎密床ポリ゚チレンが䜿甚できる。ポリプロ
ピレンはアむ゜タクチツクポリプロピレンのほ
か、副生物の非結晶性アタクチツクポリプロピレ
ンも䜿甚できる。 ゚チレン・アクリル酞共重合䜓以䞋EAAず
いうぱチレンずアクリル酞ずの高圧重合反応
で補造されるもので、アクリル酞の含有量は〜
20重量のものが奜たしい。゚チレン・゚チルア
クリレヌト共重合䜓以䞋EEAずいうぱチ
ルアクリレヌトの含有量が〜25重量皋床のも
の、゚チレン・酢酞ビニル共重合䜓以䞋EVA
ずいうは酢酞ビニルの含有量が〜30のもの
が奜たしい。これ等各暹脂のメルトむンデツクス
は〜500皋床のものが奜たしい。 (c)の導電性充填材ずしおは、その䜓積抵抗が30
Ω・cm以䞋のものであればいずれも䜿甚できる。
䜓積抵抗が30Ω・cm以䞋の導電性充填剀ずしおは
カヌボンブラツク、グラフアむト粉、銀粉、銅
粉、ニツケル粉、アルミ粉、亜鉛末、ステンレス
粉、リン化鉄粉、銅―銀耇合粉、ニツケル―銀耇
合粉、アルミフレヌク、ステンレスフレヌク、ニ
ツケルフレヌク、亜鉛フレヌク、リン片状グラフ
アむト、カヌボンフアむバヌ、アルミフアむバ
ヌ、ステンレスフアむバヌ、黄銅フアむバヌ、カ
ヌボンスフむアヌ、銀コヌトガラスビヌズ、銀コ
ヌトガラスフアむバヌ等があり、これらはいずれ
も䜿甚できる。ただこれらの䟡栌面、垂堎性及び
溶接匷床よりカヌボンブラツク、カヌボンフアむ
バヌ、グラフアむト粉、リン片状グラフアむト、
リン化鉄、ステンレス粉、ステンレスフレヌク、
亜鉛末及びリン片状亜鉛末が奜たしい。 カヌボンブラツクはアセチレンブラツク、フア
ヌネスブラツクのいずれも䜿甚できるが、導電性
の点からは高次ストラクチダヌである鎖状構造を
䜜り易いアセチレンブラツクの方が奜たしい。カ
ヌボンフアむバヌは、ポリアクリロニトリルを原
料ずするPAN系ずピツチ系があるが、本発明に
はいずれも䜿甚できる。カヌボンフアむバヌの繊
維埄は10〜30ÎŒm、繊維長は0.05〜mmが奜たし
い。 その他の各皮フアむバヌずしおは繊維埄10〜
30ÎŒm、繊維長0.05〜mm皋床のものが奜たしく
䜿甚される。たた䞊蚘各皮粉末のサむズずしおは
粉埄0.02〜500ÎŒm皋床、フレヌク䞊びにリン片状
導電性のサむズは厚さ0.1〜50ÎŒm、粒埄〜
1000ÎŒm皋床のものが奜たしい。 䞊蚘各成分の内、(a)に蚘した成分は、組成物に
優れた防錆力を付䞎するための成分であり、酞化
ペトロラタム、酞化ワツクス、これらの金属塩又
ぱステル、ラノリン金属塩及び石油スルホン
酞、又は合成スルホン酞の金属塩の少なくずも
皮、20〜80郚、奜たしくは30〜70郚、ペトロラタ
ム、ラノリン及びワツクスの少なくずも皮、20
〜80郚、奜たしくは30〜70郚よりなる混合物を10
〜90郚、奜たしくは20〜70郚䜿甚する。前者ず埌
者の割合が、2080未満の堎合は、密着性及び防
錆力が悪くなり、8020を超えた堎合は、塗膜に
粘着性が残り、たた極性が匷くなる結果、耐氎性
及び耐湿性が悪くなるので奜たしくない。 (b)に蚘した成分の合成暹脂は、組成物に物理的
匷床䞊びに可撓性を持たせるための成分であり、
ポリ゚チレン、ポリプロピレン、EAA、EEA、
EVAの少なくずも皮を10〜90郚、奜たしくは
30〜80郚䜿甚する。(a)成分ず(b)成分の混合割合が
1090未満の堎合は、本発明所期の防錆力が埗ら
れず、9010を超えた堎合は、塗膜の耐屈曲性、
匕匵り匷さ等の物理的匷床が劣るので奜たしくな
い。 (c)成分は塗膜の䜓積抵抗を䞋げ、優れた点溶接
性を付䞎するための成分で、(a)ず(b)の和100郚に
察しお、䜓積抵抗30Ω・cm以䞋の導電性充填材を
10〜300郚、奜たしくは30〜250郚䜿甚する。導電
性充填材が10郚未満の堎合は点溶接性が悪くな
り、300郚より倚いず、塗膜が脆くなり、たた溶
融粘床が高くな぀お塗装䜜業性が悪くなるので奜
たしくない。 本発明の組成物においおは、䞊蚘各成分の他
に、この皮の組成物に通垞䜿甚される各皮の成分
を、必芁に応じお、適宜䜿甚するこずができる。
そのような成分ずしおは、䟋えば石油暹脂、環化
ゎム、クマロンむンデン暹脂、ポリブテン暹脂等
の䞊蚘各成分ず盞溶性のある合成暹脂、酞化錫、
酞化亜鉛等の金属酞化物、二酞化チタン、ベンガ
ラ等の着色顔料、タルク、炭酞カルシりム、カオ
リンクレヌ等の䜓質顔料、消泡剀、分散剀等を挙
げるこずができる。 本発明の組成物は、(a)及び(b)成分を、加熱溶融
䞋に混合した埌、これに(c)成分を加えお、䟋えば
デむゟルバヌ、加熱ロヌルミル等を甚いお分散、
混合しお補造される。 斯くしお埗られる本発明のり゚ルダブルホツト
メルト防錆剀組成物は、䞀般のホツトメルトアプ
リケヌタヌにより、点溶接重ね合せ面に塗垃でき
るほか、予め䞀定サむズのフむルム又はシヌトに
したものを点溶接重ね合せ面に挟んで点溶接した
埌、䞀定枩床に加熱溶融する方法で䜿甚できる。 本発明のり゚ルダブルホツトメルト防錆剀は、
防錆力及び点溶接性に優れ、しかも塗膜の密着
性、物理的匷床、耐氎性及び耐湿性が良奜である
ほか、䜿甚時の火灜の危険性䞊びに人䜓に察する
衛生䞊の問題がなく、䜜業性が良奜であるので、
車茌、電気機噚、各皮機械、事務機噚、鋌補家
具、建材等の殆んどの金属加工業で䜿甚でき、点
溶接重ね合せ面の防錆に優れた効果を発揮する。 本発明組成物を甚いお点溶接するに際しおはそ
の手段ずしおは特に限定されるものではないが、
点溶接重ね合せ面に本発明組成物を介圚させお点
溶接を行うのが奜たしい。曎に詳しくは、点溶接
重ね合せ面に本発明組成物を茉眮し、点溶接を行
な぀た埌、該組成物を加熱溶融する方法、点溶接
重ね合せ面に該組成物を加熱溶融しお塗垃し、次
いで点溶接を行う方法、該組成物を予めシヌトた
たはフむルム状ずなし、このシヌトたたはフむル
ムを点溶接重ね合せ面に介圚せしめ、点溶接を行
う方法、該組成物を粉末の状態ずしお点溶接重ね
合せ面に介圚せしめる方法等を䟋瀺出来る。 以䞋実斜䟋を瀺すが、本発明は以䞋の実斜䟋の
みに限定されるものではない。なお実斜䟋䞭の郚
は重量郚を、は重量を瀺す。 実斜䟋 〜38 䞋蚘第衚のその〜そのに瀺す配
合割合の(a)及び(b)の各成分を、200℃の加熱䞋に
デむゟルバヌで撹拌混合した埌第衚のその
に瀺す(c)成分を加え、曎にデむゟルバヌで撹
拌混合しお本発明のり゚ルダブルホツトメルト防
錆剀組成物を埗た。
The present invention relates to a weld double hot melt rust preventive composition, and more particularly to a composition used for the rust prevention of spot welded overlapping surfaces. It is an object of the present invention to provide a weldable hot melt rust preventive composition that has good film adhesion, physical strength, water resistance, and moisture resistance. Conventionally, spot welding has been widely used in most metal processing industries because it is a very simple and efficient method of joining metal plates. For the most part, this is done untreated and naked. As a result, spot welding overlapping surfaces are prone to rust, and since it is impossible to completely prevent rust after welding, we have created a rust preventive for spot welding overlapping surfaces with excellent rust prevention power and weldability. The development of drugs has been a major challenge for many years. Currently, zinc-rich paint is used in some parts of the industry to prevent rust on spot welded overlapping surfaces, but since it is a solvent-based paint, there is a risk of fire due to organic solvents and hygienic problems for the human body. However, it has not yet become widely popular. In addition, the two-coat zinc chrome metal formulation is made by baking an epoxy resin zinc-rich paint onto a steel plate coated with a chemical solution containing chromic acid and zinc powder, etc., and has excellent rust prevention properties and good spot weldability. Therefore, it is used as a rust prevention treatment that can be spot welded, but the painting process is two steps and the baking temperature is very high, resulting in poor workability. others,
Due to the toxicity of chromic acid, it is rarely used as a rust preventive agent for spot welded mating surfaces. The present inventor focused on the above-mentioned drawbacks of conventional products, and found that they do not have the drawbacks due to the use of organic solvents, have good workability (can be done in one step instead of two steps), and meet the requirements for a weldable rust preventive agent. For example, as a result of continuing research to develop a rust preventive agent and a rust preventive agent that has good weldability and excellent paint film adhesion, water resistance, and moisture resistance, the present invention has been completed. The invention comprises (a) 20 to 80 parts by weight of at least one of petrolatum oxide, wax oxide, metal salts or esters thereof, metal salts of lanolin, and metal salts of petroleum sulfonic acids or synthetic sulfonic acids; petrolatum;
At least one of lanolin and wax, 20~
mixture consisting of 80 parts by weight, 10 to 90 parts by weight, (b) polyethylene, polypropylene, ethylene.
10 to 90 parts by weight of at least one of acrylic acid copolymer, ethylene/ethyl acrylate copolymer, and ethylene/vinyl acetate copolymer, and (a)
For 100 parts by weight of (b), (c) conductive filler with a volume resistance of 30Ω・cm or less, 10~
This relates to a weldable hot melt rust preventive composition characterized in that it contains 300 parts by weight. Petrolatum oxide, oxidized wax, metal salts or esters thereof, lanolin metal salts, metal salts of petroleum sulfonic acid or synthetic sulfonic acid, petrolatum, lanolin, and wax used in the present invention include general wax-based preventive agents. What has traditionally been used as rust paint can be used in a wide range of applications.
Among them, those having a softening point of about 40 to 180°C can be preferably used. Furthermore, the metal of each metal salt in each of the above components is not particularly limited, and many metals can be used, such as alkali metals such as sodium, potassium, and lithium, alkaline earths such as calcium, barium, and strontium. Examples include similar metals, molybdenum, zinc, and the like. Among these, alkali metals and alkaline earth metals are preferred from the viewpoint of antirust effect. Of course, these metal salts may contain one kind of metal or two or more kinds of metals. As the polyethylene component (b), high-density polyethylene and low-density polyethylene can be used. As the polypropylene, in addition to isotactic polypropylene, amorphous atactic polypropylene as a by-product can also be used. Ethylene-acrylic acid copolymer (hereinafter referred to as EAA) is produced by high-pressure polymerization reaction of ethylene and acrylic acid, and the content of acrylic acid is 1 to 1.
20% by weight is preferred. Ethylene/ethyl acrylate copolymer (hereinafter referred to as EEA) has an ethyl acrylate content of approximately 5 to 25% by weight, and ethylene/vinyl acetate copolymer (hereinafter referred to as EVA)
) preferably has a vinyl acetate content of 5 to 30%. The melt index of each of these resins is preferably about 5 to 500. The conductive filler (c) has a volume resistivity of 30
Any material with a resistance of Ω・cm or less can be used.
Examples of conductive fillers with a volume resistivity of 30Ω・cm or less include carbon black, graphite powder, silver powder, copper powder, nickel powder, aluminum powder, zinc powder, stainless steel powder, iron phosphide powder, copper-silver composite powder, and nickel. -Silver composite powder, aluminum flakes, stainless steel flakes, nickel flakes, zinc flakes, flaky graphite, carbon fibers, aluminum fibers, stainless fibers, brass fibers, carbon spheres, silver coated glass beads, silver coated glass fibers, etc. Yes, any of these can be used. However, due to the price, marketability, and welding strength of these materials, carbon black, carbon fiber, graphite powder, flaky graphite,
iron phosphide, stainless steel powder, stainless steel flakes,
Zinc dust and flaky zinc dust are preferred. As the carbon black, either acetylene black or furnace black can be used, but from the viewpoint of electrical conductivity, acetylene black is preferable because it can easily form a chain structure, which is a higher-order structure. There are two types of carbon fibers, PAN type and Pitch type, both of which are made from polyacrylonitrile, and both can be used in the present invention. The carbon fiber preferably has a fiber diameter of 10 to 30 ÎŒm and a fiber length of 0.05 to 1 mm. For other various fibers, the fiber diameter is 10~
A fiber having a fiber length of about 30 ÎŒm and a fiber length of about 0.05 to 1 mm is preferably used. In addition, the sizes of the various powders mentioned above are approximately 0.02 to 500 ÎŒm in diameter, and the sizes of flakes and scale-like conductive powders are 0.1 to 50 ÎŒm in thickness and particle diameters of 2 to 500 ÎŒm.
A thickness of about 1000 ÎŒm is preferable. Among the above-mentioned components, the component listed in (a) is a component for imparting excellent rust-preventive power to the composition, and includes petrolatum oxide, wax oxide, metal salts or esters thereof, lanolin metal salts, and petroleum oxide. At least one metal salt of sulfonic acid or synthetic sulfonic acid
seeds, 20-80 parts, preferably 30-70 parts, at least one of petrolatum, lanolin and wax, 20
10 of a mixture consisting of ~80 parts, preferably 30-70 parts
~90 parts are used, preferably 20-70 parts. If the ratio of the former to the latter is less than 20:80, the adhesion and rust prevention will be poor, and if it exceeds 80:20, the paint film will remain sticky and the polarity will become strong, resulting in poor water resistance. This is not preferable because the properties and moisture resistance deteriorate. The synthetic resin component described in (b) is a component for imparting physical strength and flexibility to the composition,
Polyethylene, polypropylene, EAA, EEA,
10 to 90 parts of at least one type of EVA, preferably
Use 30-80 copies. The mixing ratio of component (a) and component (b) is
If the ratio is less than 10:90, the desired rust prevention ability of the present invention will not be obtained, and if it exceeds 90:10, the bending resistance of the coating film will be affected.
It is not preferred because it has poor physical strength such as tensile strength. Component (c) is a component that lowers the volume resistance of the coating film and gives it excellent spot welding properties, and it has a conductivity with a volume resistance of 30Ω・cm or less per 100 parts of the sum of (a) and (b). filling material
10 to 300 parts are used, preferably 30 to 250 parts. If the amount of the conductive filler is less than 10 parts, the spot weldability will be poor, and if it is more than 300 parts, the coating film will become brittle and the melt viscosity will become high, resulting in poor painting workability, which is not preferable. In the composition of the present invention, in addition to the above-mentioned components, various components commonly used in this type of composition can be used as appropriate.
Such components include, for example, petroleum resins, cyclized rubber, coumaron indene resins, polybutene resins, and other synthetic resins that are compatible with each of the above components, tin oxide,
Examples include metal oxides such as zinc oxide, color pigments such as titanium dioxide and red iron oxide, extender pigments such as talc, calcium carbonate, and kaolin clay, antifoaming agents, and dispersants. The composition of the present invention is prepared by mixing components (a) and (b) under heating and melting, then adding component (c) thereto, and dispersing the mixture using, for example, a dissolver, a heated roll mill, etc.
Produced by mixing. The thus obtained weldable hotmelt rust preventive composition of the present invention can be applied to spot welded overlapping surfaces using a general hotmelt applicator, or it can be applied to spot welded overlapping surfaces by pre-forming a film or sheet of a certain size and spot welding overlapping. It can be used by spot welding by sandwiching it between mating surfaces and then heating and melting it to a constant temperature. The well double hot melt rust preventive agent of the present invention is
It has excellent rust prevention and spot welding properties, as well as good paint film adhesion, physical strength, water resistance and moisture resistance, and there is no risk of fire or hygienic problems to the human body during use, making it easy to work with. Because the properties are good,
It can be used in most metal processing industries such as vehicles, electrical equipment, various machines, office equipment, steel furniture, building materials, etc., and has excellent rust prevention effects on spot welded overlapping surfaces. When performing spot welding using the composition of the present invention, the means for spot welding is not particularly limited, but
Spot welding is preferably performed with the composition of the present invention interposed between the overlapping surfaces. More specifically, a method of placing the composition of the present invention on a spot-welded overlapping surface, performing spot welding, and then heating and melting the composition; A method in which the composition is applied in the form of a sheet or film in advance, this sheet or film is interposed between the spot welding overlapping surfaces, and spot welding is performed; a method in which the composition is in the form of a powder; Examples include a method of intervening spot welds on overlapping surfaces. Examples will be shown below, but the present invention is not limited to the following examples. Note that in the examples, parts indicate parts by weight, and percentages indicate weight %. Examples 1 to 38 The components (a) and (b) in the proportions shown in (Part 1) to (Part 2) of Table 1 below were stirred and mixed with a dissolver while heating at 200°C. Component (c) shown in Table (Part 3) was added and further stirred and mixed using a dissolver to obtain a weldable hot melt rust preventive composition of the present invention.

【衚】【table】

【衚】【table】

【衚】【table】

【衚】【table】

【衚】【table】

【衚】 比范䟋 〜11 防錆剀組成を第衚に瀺したものに代えたほか
は、実斜䟋〜36ず同様にしお比范のり゚ルダブ
ルホツトメルト防錆剀組成物を埗た。
[Table] Comparative Examples 1 to 11 Comparative weld double hot melt rust preventive compositions were obtained in the same manner as Examples 1 to 36, except that the rust preventive composition was changed to that shown in Table 2.

【衚】【table】

【衚】 実斜䟋及び比范䟋によ぀お埗た各り゚ルダブル
ホツトメルト防錆剀の特性を、以䞋に述べる方法
により詊隓し、評䟡した。 (1) 詊隓片は、鋌板70×1.50×mmの片面
に、200℃に加熱溶融した詊料を、膜厚200ÎŒm
にヘラ塗り回塗りし、宀枩20℃に攟
冷しお詊隓片ずした。 点溶接性詊隓片は、枚の鋌板70×150×
0.8mmの枚に、長蟺に平行に、端から25mm
の幅に、200℃に加熱溶融した詊料を、膜厚
200ÎŒmにヘラ塗りし、盎ちに、もう枚の鋌板
をその䞊に、同じ幅で重ね合せお接着し詊隓片
ずした。 (2) 防錆力の詊隓ずしおは、塩氎噎霧詊隓及び耐
塩氎性詊隓を行぀た。 塩氎噎霧詊隓は、JIS  2371の塩氎噎霧詊
隓方法に埓぀お1000時間詊隓し、詊隓片の発錆
の皋床を芳察した。耐塩氎性は、詊隓片を20℃
の塩化ナトリりム氎溶液にカ月浞挬した
埌、塗膜の状態を芳察した。その結果を異状な
し〇、やや防錆△、かなり防錆×の
段階に分けお評䟡した。 (3) 密着性は、JIS  6909合成暹脂゚マルゞ
ペン砂壁状吹付材―5.5付着匷さの詊隓方法
にしたが぀お詊隓を行い付着匷さが単䜍Kgcm2
で衚わしお以䞊を〇、以䞊未満を
△、未満を×に分けお評䟡した。 (4) 粘着性は、塗面を指頭で觊れお状態を調査
し、粘着性なし〇、僅か粘着△、皍粘着
×の段階に分けお評䟡した。 (5) 耐氎性、詊隓片を20℃の氎道氎にカ月浞挬
した埌、塗膜の状態を芳察し、異状なし〇、
皍軟化膚最△、かなり軟化膚最×の
段階に分けお評䟡した。 (6) 耐湿性は、詊隓片を50℃、98R.H.の耐湿
詊隓噚に入れ、カ月詊隓した埌、塗膜の状態
を芳察し、異状なし〇、皍軟化膚最△、
かなり軟化膚最×の段階に分けお評䟡し
た。 (7) 塗膜の物理的匷床の詊隓ずしおは、匕匵詊隓
ず耐屈曲性詊隓を行぀た。 匕匵詊隓は、JIS  6301―加硫ゎム物
理詊隓方法、匕匵詊隓に埓぀お詊隓を行い、
その結果を単䜍Kgcm2で衚わし、10以䞊を
〇、以䞊10未満を△、未満を×、
耐屈曲性は、詊隓片を盎埄20φmmの金属棒にそ
぀お折曲げお塗膜の状態を芳察した。その結果
を異状なし〇、僅かひび割れ△、かなり
ひび割れ×のそれぞれ段階に分けお評䟡
した。 (9) 点溶接性は、条件で点溶接できる堎合を
〇、条件ではできないが条件でできる堎
合を△、条件でもできない堎合を×
の段階に分けお評䟡した。
[Table] The properties of each well double hot melt rust preventive agent obtained in Examples and Comparative Examples were tested and evaluated by the method described below. (1) The test piece is a 200 ÎŒm thick film of a sample heated and melted at 200℃ on one side of a steel plate (70 x 1.50 x 2 mm).
It was coated with a spatula (one coat) and allowed to cool to room temperature (20°C) to prepare a test piece. The spot weldability test pieces were made of two steel plates (70×150×
0.8mm) parallel to the long side, 25mm from the edge.
A sample heated and melted at 200℃ is applied to the width of
After coating with a spatula to a thickness of 200 ÎŒm, another steel plate was immediately placed on top of it with the same width and adhered to form a test piece. (2) As a test for rust prevention ability, a salt spray test and a salt water resistance test were conducted. The salt spray test was conducted for 1000 hours according to the salt spray test method of JIS Z 2371, and the degree of rust on the test piece was observed. Salt water resistance test specimens at 20℃
After being immersed in a 3% sodium chloride aqueous solution for 3 months, the condition of the coating film was observed. The results were divided into three grades: no abnormality (○), somewhat rust-proof (△), and considerably rust-proof (x). (3) Adhesion was tested according to JIS A 6909 (Synthetic resin emulsion sand wall spray material) - 5.5 Adhesion strength test method, and the adhesion strength was measured in kg/cm 2
The evaluation was divided into 7 or more (○), 4 or more and less than 7 (△), and less than 4 (x). (4) Adhesiveness was evaluated by touching the coated surface with the tip of a finger and dividing it into three grades: no tackiness (〇), slightly tackiness (△), and slightly tackiness (×). (5) Water resistance: After immersing the test piece in tap water at 20°C for one month, the state of the coating film was observed. No abnormality (〇);
Slight softening and swelling (△), considerable softening and swelling (×) 3
The evaluation was divided into stages. (6) Moisture resistance is determined by placing the test piece in a humidity tester at 50℃ and 98%RH, and observing the condition of the coating after testing for one month.No abnormality (〇), slight softening and swelling (△)
The evaluation was divided into three stages: considerable softening and swelling (×). (7) A tensile test and a bending resistance test were conducted to test the physical strength of the coating film. The tensile test was conducted in accordance with JIS K 6301-3 (vulcanized rubber physical test method, tensile test).
The results are expressed in Kg/ cm2 , with 10 or more (○), 5 or more and less than 10 (△), and less than 5 (×).
The bending resistance was determined by bending a test piece along a metal rod with a diameter of 20 mm and observing the state of the coating film. The results were divided into three grades: no abnormality (○), slight cracking (△), and considerable cracking (x). (9) For spot weldability, if spot welding is possible under condition a (○), if it is not possible under condition a but possible under condition b (△), if it is not possible even under condition b (×)
The evaluation was divided into three stages.

【衚】 これらの詊隓結果を䞋蚘第衚に瀺す。【table】 The results of these tests are shown in Table 4 below.

【衚】【table】

【衚】 第衚に挙げた詊隓結果から明らかなごずく、
実斜䟋〜36で埗られた本発明のり゚ルダブルホ
ツトメルト防錆剀組成物は、すべおの詊隓項目に
おいお良奜な結果が埗られ、防錆力、点溶接性、
密着性、物理的匷床、耐氎性及び耐湿性にすぐれ
おいるこずが実蚌された。 これに察しお、(a)成分䞭の酞化ペトロラタム、
酞化ワツクス、これらの金属塩又ぱステル、ラ
ノリン金属塩及び石油スルホン酞又は合成スルホ
ン酞の金属塩の少なくずも皮ず、ペトロラタ
ム、ラノリン及びワツクスの少なくずも皮ずの
混合割合が、8020を超えた比范䟋の組成物
は、塗膜に粘着性が残り、耐氎性及び耐湿性が劣
り、たた2080未満の比范䟋の組成物は、防錆
力、密着性が劣るこず、(a)成分を䜿甚しないか、
(a)成分ず(b)成分の割合が、1090未満の比范䟋
、は防錆力が劣るこず、(b)成分を䜿甚しない
か、(a)成分ず(b)成分の割合が9010を超えた比范
䟋、は耐屈曲性、匕匵り匷さ等の物理的匷床
が劣るこず、(c)成分を䜿甚しないか、(a)ず(b)の和
100郚に察しお(c)成分の添加量が10郚未満の比范
䟋〜のものは、点溶接性が劣るこず、(c)成分
の添加量が、300郚を超えた比范䟋10、11の組成
物は塗膜の耐屈曲性が劣るこずが、同じく第衚
から明らかである。
[Table] As is clear from the test results listed in Table 4,
The weldable hotmelt rust preventive compositions of the present invention obtained in Examples 1 to 36 showed good results in all test items, including excellent rust prevention ability, spot weldability,
It was demonstrated that it has excellent adhesion, physical strength, water resistance, and moisture resistance. On the other hand, petrolatum oxide in component (a),
The mixing ratio of at least one of oxidized wax, metal salt or ester thereof, lanolin metal salt, and metal salt of petroleum sulfonic acid or synthetic sulfonic acid and at least one of petrolatum, lanolin, and wax exceeds 80:20. The composition of Comparative Example 1, which had a ratio of less than 20:8, had poor anti-corrosion ability and adhesion. a) do not use ingredients or
Comparative Examples 3 and 4, in which the ratio of component (a) to component (b) is less than 10:90, have poor rust prevention ability. Comparative Examples 5 and 6 where the ratio exceeds 90:10 have poor physical strength such as bending resistance and tensile strength, and either component (c) is not used or the sum of (a) and (b)
Comparative Examples 7 to 9 in which the amount of component (c) added was less than 10 parts per 100 parts had poor spot welding properties, and Comparative Example 10 in which the amount of component (c) added exceeded 300 parts. It is also clear from Table 4 that the compositions of Nos. 1 and 11 have poor bending resistance of the coating film.

Claims (1)

【特蚱請求の範囲】  (a) 酞化ペトロラタム、酞化ワツクス、これ
らの金属塩又ぱステル、ラノリン金属塩、及
び石油スルホン酞又は合成スルホン酞の金属塩
の少なくずも皮、20〜80重量郚、ペトロラタ
ム、ラノリン及びワツクスの少なくずも皮、
20〜80重量郚よりなる混合物、10〜90重量郚、 (b) ポリ゚チレン、ポリプロピレン、゚チレン・
アクリル酞共重合䜓、゚チレン・゚チルアクリ
レヌト共重合䜓、゚チレン・酢酞ビニル共重合
䜓の少なくずも皮、10〜90重量郚、及び(a)ず
(b)の和100重量郚に察しお、 (c) 䜓積抵抗30Ω・cm以䞋の導電性充填材、10〜
300重量郹 を含有しおなるこずを特城ずするり゚ルダブルホ
ツトメルト防錆剀組成物。  䞊蚘金属の金属塩が、アルカリ金属又は及
びアルカリ土類金属である特蚱請求の範囲第項
蚘茉のり゚ルダブルホツトメルト防錆剀組成物。  䞊蚘導電性充填剀が、カヌボンブラツク、カ
ヌボンフアむバヌ、グラフアむト粉、リン片状グ
ラフアむト、リン化鉄粉、ステンレス粉、ステン
レスフレヌク、亜鉛末及びリン片状亜鉛末の少な
くずも皮である特蚱請求の範囲第項又は第
項蚘茉のり゚ルダブルホツトメルト防錆剀組成
物。
[Scope of Claims] 1 (a) At least one of petrolatum oxide, wax oxide, metal salts or esters thereof, metal salts of lanolin, and metal salts of petroleum sulfonic acids or synthetic sulfonic acids, 20 to 80 parts by weight, petrolatum , at least one of lanolin and wax;
mixture consisting of 20 to 80 parts by weight, 10 to 90 parts by weight, (b) polyethylene, polypropylene, ethylene.
10 to 90 parts by weight of at least one of acrylic acid copolymer, ethylene/ethyl acrylate copolymer, and ethylene/vinyl acetate copolymer, and (a)
For 100 parts by weight of (b), (c) conductive filler with a volume resistance of 30Ω・cm or less, 10~
300 parts by weight of a well double hot melt rust preventive composition. 2. The weldable hot melt rust preventive composition according to claim 1, wherein the metal salt of the metal is an alkali metal or/and an alkaline earth metal. 3. A patent in which the conductive filler is at least one of carbon black, carbon fiber, graphite powder, scaly graphite, iron phosphide powder, stainless steel powder, stainless steel flakes, zinc powder, and scaly zinc powder. Claim 1 or 2
The well double hot melt rust preventive composition described in Section 1.
JP58216948A 1983-11-17 1983-11-17 Weldable hot-melt rust preventive agent composition Granted JPS60108445A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58216948A JPS60108445A (en) 1983-11-17 1983-11-17 Weldable hot-melt rust preventive agent composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58216948A JPS60108445A (en) 1983-11-17 1983-11-17 Weldable hot-melt rust preventive agent composition

Publications (2)

Publication Number Publication Date
JPS60108445A JPS60108445A (en) 1985-06-13
JPS6362546B2 true JPS6362546B2 (en) 1988-12-02

Family

ID=16696432

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58216948A Granted JPS60108445A (en) 1983-11-17 1983-11-17 Weldable hot-melt rust preventive agent composition

Country Status (1)

Country Link
JP (1) JPS60108445A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6373365U (en) * 1986-10-31 1988-05-16
JP2665525B2 (en) * 1991-07-04 1997-10-22 ナシロ化孊工業株匏䌚瀟 Undercoat agent composition
KR20030043075A (en) * 2001-11-26 2003-06-02 걎섀화학공업(죌) Pyrolysis-natured antirust oil composition for fin tube

Also Published As

Publication number Publication date
JPS60108445A (en) 1985-06-13

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