JPS6045672B2 - hot melt adhesive composition - Google Patents
hot melt adhesive compositionInfo
- Publication number
- JPS6045672B2 JPS6045672B2 JP9481779A JP9481779A JPS6045672B2 JP S6045672 B2 JPS6045672 B2 JP S6045672B2 JP 9481779 A JP9481779 A JP 9481779A JP 9481779 A JP9481779 A JP 9481779A JP S6045672 B2 JPS6045672 B2 JP S6045672B2
- Authority
- JP
- Japan
- Prior art keywords
- nylon
- hot melt
- adhesive composition
- adhesive
- melt adhesive
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】
本発明はホットメルト接着剤組成物に関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to hot melt adhesive compositions.
従来より、ポリエチレン、エチレン酢酸ビニル共重合体
、、アイオノマー、ナイロン等の熱可塑性樹脂を材料と
するホットメルト接着剤は多数知られている。Many hot melt adhesives made from thermoplastic resins such as polyethylene, ethylene-vinyl acetate copolymers, ionomers, and nylon have been known.
しかし、ポリエチレン、エチレン酢酸ビニル共重合体、
アイオノマー等は金属などの接着に使用した場合充分な
接着強度が得られず実用に供し難かつた。However, polyethylene, ethylene vinyl acetate copolymer,
When ionomers and the like are used for adhering metals, etc., sufficient adhesion strength cannot be obtained, making it difficult to put them into practical use.
又、ナイロンについては金属に対し或る程度の接着強度
は有するがいまだ充分でなく、そのためナイロンにエポ
キシ樹脂等を配合したり、又はナイロンフィルムの両面
にエポキシ樹脂をコーティングしたいわゆるナイロン−
エポキシ系のホットメルト接着剤が提案されている、こ
の様な接着剤は硬化の完了にかなりの長時間を要し、又
、コスト的にも高くつくので、一般的な用途の接着剤と
しては適当でない。又、ナイロンにエチレン−酢酸ビニ
ル共重合体がアイオノマー等を混合することにより接着
強度を向上させようとする試みもなされているが、いず
れの場合も接着強度向上についての満足すべき成果が得
られておらず、さらに該強度の向上が望まれている。本
発明はかゝる現状にかんがみ、金属等に対する接着強度
にすぐれ、使いやすく、しかも安価なホットメルト接着
剤組成物を提供することを目的としてなされたものであ
り、その要旨はナイロン系重合体100重量部に対しポ
リテトラフロロエチレンが1〜20腫量部混合されてな
るこを特徴とするホットメルト接着剤組成物に存する。Although nylon has a certain degree of adhesive strength to metals, it is still not sufficient, so nylon is mixed with epoxy resin, or so-called nylon film is coated with epoxy resin on both sides of the nylon film.
Epoxy-based hot melt adhesives have been proposed; however, such adhesives require a considerable amount of time to complete curing and are expensive, so they are not suitable for general use. It's not appropriate. In addition, attempts have been made to improve adhesive strength by mixing nylon with ethylene-vinyl acetate copolymer ionomers, etc., but in all cases, satisfactory results in improving adhesive strength have not been obtained. However, it is desired to further improve the strength. In view of the current situation, the present invention has been made for the purpose of providing a hot melt adhesive composition that has excellent adhesive strength to metals, etc., is easy to use, and is inexpensive. A hot melt adhesive composition characterized in that 1 to 20 parts by volume of polytetrafluoroethylene is mixed with 100 parts by weight.
本発明においてナイロン系重合体とは一般にナイロンと
呼称されており、従来においてホットメルト接着剤とし
て用いることが知られている。In the present invention, the nylon polymer is generally referred to as nylon, and is conventionally known to be used as a hot melt adhesive.
たとえばナイロン12、ナイロン11)ナイロン6、ナ
イロン66、ナイロン610やこれらの共重合体を指す
ものである。又、本発明においてナイロン系重合体に混
合するポリテトラフロロエチレンは微粒子の形状で用い
られるのがよく、その好適な粒子径は100ミク゛ロン
以下である。For example, it refers to nylon 12, nylon 11) nylon 6, nylon 66, nylon 610, and copolymers thereof. Further, in the present invention, the polytetrafluoroethylene to be mixed with the nylon polymer is preferably used in the form of fine particles, and the preferred particle size is 100 microns or less.
本発明接着剤組成物を製造するには前記ナイロン系重合
体と前記ポリテトラフロロエチレンとを加え合せて混合
して適宜な形状のものとすればよく、例えばこれらの重
合体の粉末或いはペレット・状のものを混合して、押出
機にかけフィルム状、線状、ペレット状に成形するとか
、ロール、ニーダー、パンバリ−ミキサー等により混練
しシート状等に成形する方法が好適に採用出来る。そし
て、前記ナイロン系重合体とポリテトラフロロエチレン
との使用量ついては、前者10鍾量部に対して後者を1
〜200重量部の範囲て用いるこを必要とする。In order to produce the adhesive composition of the present invention, the nylon polymer and the polytetrafluoroethylene may be added and mixed to form a suitable shape, for example, powder or pellets of these polymers. Preferred methods include mixing the mixture and applying it to an extruder to form it into a film, line, or pellet, or kneading it using a roll, kneader, panball mixer, etc. and forming it into a sheet or the like. Regarding the amount of the nylon polymer and polytetrafluoroethylene used, the latter is 1 part by weight for every 10 parts by weight of the former.
It is necessary to use it in a range of 200 parts by weight.
その理由は、ポリテトラフロロエチレンの使用量が1重
量部未満の場合は得られる接着剤組成物の剥離強度の増
大という効果が発現されず、200重量部を越える場合
は、ナイロン系重合体との混和性の限界を越えるためと
推測されるが、剥離強度が低下する傾向にあるからてあ
る。The reason for this is that if the amount of polytetrafluoroethylene used is less than 1 part by weight, the effect of increasing the peel strength of the resulting adhesive composition will not be achieved, and if it exceeds 200 parts by weight, the nylon polymer will This is presumed to be due to exceeding the limit of miscibility, but it is also because the peel strength tends to decrease.
本発明接着剤組成物は一般のホットメルト接着剤と同様
な用途に使用されることが出来るが、特に鉄、アルミニ
ウム、銅、真ちゆうなどの金属材料、ガラス、陶磁器、
スレート、コンクリートなどの無機材料、木綿、絹、羊
毛、テトロン、ナイロン繊維などの繊維材料や紙製品な
どのを接着するのに使用されてすぐれた特性を発揮して
得る。The adhesive composition of the present invention can be used for the same purposes as general hot-melt adhesives, but in particular metal materials such as iron, aluminum, copper, and brass, glass, ceramics, etc.
It exhibits excellent properties and is used to bond inorganic materials such as slate and concrete, fibrous materials such as cotton, silk, wool, Tetoron and nylon fibers, and paper products.
なお本発明接着剤組成物には、着色剤、充填剤等の添加
剤が必要に応じ加えられてもさしつかえない。本発明の
ホットメルト接着剤組成物は上述の通りの構成のもので
あるが、すぐれた接着強度を示すことを出来るものてあ
る。Note that additives such as colorants and fillers may be added to the adhesive composition of the present invention as necessary. The hot melt adhesive composition of the present invention has the above-mentioned structure, and is capable of exhibiting excellent adhesive strength.
以下本発明の実施例について説明する。Examples of the present invention will be described below.
実施例1
共重合ナイロン(融点11rC1メルトインデックス3
5)と微粒子状のポリテトラフロロエチレン(融点32
3゜C、最大粒径24ミクロン)とを第1表に示す割合
で配合し、押出機により厚さ100ミクロ.ンのフィル
ム状に押出して、フィルム状接着剤となした。Example 1 Copolymerized nylon (melting point 11rC1 melt index 3
5) and finely divided polytetrafluoroethylene (melting point 32
3°C, maximum particle size 24 microns) in the proportions shown in Table 1, and extruded to a thickness of 100 microns. A film adhesive was made by extruding it into a film.
次にこの接着剤をアセトン脱脂した厚さ0.6胴の2枚
の亜鉛銅板の間におき、温度120℃、加圧2k9k漬
、2分間の接着条件で該鋼板同志を接着し、接着後20
゜Cて相対湿度60%の条件下に3。日間放置した。か
くして接着された亜鉛銅板のT剥離強度を測定した。Next, this adhesive was placed between two zinc-copper plates with a thickness of 0.6 that had been degreased with acetone, and the steel plates were bonded together at a temperature of 120°C and a pressure of 2k9k for 2 minutes. 20
3 under the conditions of 60% relative humidity at °C. I left it for days. The T-peel strength of the thus bonded zinc-copper plates was measured.
測定条件は剥離速度50TUfL/分、サンプル巾25
薗、温度20℃、湿度60%であつた。T剥離強度の測
定結果が第1表に示す。比較例1
共重合ナイロン(実施例1と同じ)を単独で用いて実施
例1と同様にして接着剤を用意し、T剥離強度を測定し
た。The measurement conditions were a peeling rate of 50 TUfL/min and a sample width of 25 mm.
The temperature was 20°C and the humidity was 60%. The measurement results of T peel strength are shown in Table 1. Comparative Example 1 An adhesive was prepared in the same manner as in Example 1 using only copolymerized nylon (same as in Example 1), and the T-peel strength was measured.
その結果は第1表の通りであつた。The results were as shown in Table 1.
比較例2
共重合ナイロン(実施例1と同じ)と重質炭酸カルシウ
ム(粒径6.3ミクロン)とを第1表に示される割合で
配合し、実施例1と同様にして接着剤を用意し、T剥離
強度を測定した。Comparative Example 2 An adhesive was prepared in the same manner as in Example 1 by blending copolymerized nylon (same as in Example 1) and heavy calcium carbonate (particle size: 6.3 microns) in the proportions shown in Table 1. Then, the T peel strength was measured.
その結果は第1表の通りであつた。実施例2
ナイロン12(融点179測C)とポリテトラフロロl
エチレン(実施例1と同じ)を第1表に示す割合で配合
し、実施例1と同様にして接着剤を用意した。The results were as shown in Table 1. Example 2 Nylon 12 (melting point: 179 C) and polytetrafluoro I
Ethylene (same as in Example 1) was blended in the proportions shown in Table 1, and an adhesive was prepared in the same manner as in Example 1.
次に接着を温度240゜C1加圧2kgId12分間の
条件て行う以外は実施例1と同様にして試料を用意し、
T剥離強度の測定を行つた。その結果は第1表に示され
る通りてあつた。比較例3
ナイロン12(実施例2と同じ)を単独て用いて接着剤
とする以外は実施例2と同様にした。Next, a sample was prepared in the same manner as in Example 1, except that bonding was performed at a temperature of 240°C, a pressure of 2kgId, and 12 minutes.
T-peel strength was measured. The results were as shown in Table 1. Comparative Example 3 The same procedure as in Example 2 was carried out except that nylon 12 (same as in Example 2) was used alone as an adhesive.
その結果は第1表の通りであつた。比較例4
ナイロン12(実施例2と同じ)と重質炭酸カルシウム
(比較例2と同じ)とを第1表に示される割合て用いて
接着剤とする以外は実施例2と同様にした。The results were as shown in Table 1. Comparative Example 4 An adhesive was prepared in the same manner as in Example 2 except that nylon 12 (same as in Example 2) and heavy calcium carbonate (same as in Comparative Example 2) were used in the proportions shown in Table 1 to form an adhesive.
その結果は第1表の通りであつた。実施例3〜6、比較
例5及び6実施例1と同様にして、第2表に記載の組成
を有する接着剤を用意し、T剥離強度を測定した。その
結果は第2表の通りであつた。尚、共重合ナイロン及び
ポリテトラフロロエチレンは実施例1と同じものを、ナ
イロン12は実施例2と同じものと、炭酸カルシウムは
比較例2と同じものを用いた。The results were as shown in Table 1. Examples 3 to 6, Comparative Examples 5 and 6 In the same manner as in Example 1, adhesives having the compositions shown in Table 2 were prepared, and the T-peel strength was measured. The results were as shown in Table 2. The copolymerized nylon and polytetrafluoroethylene were the same as in Example 1, the nylon 12 was the same as in Example 2, and the calcium carbonate was the same as in Comparative Example 2.
実施例7〜9実施例1と同様にして、第3表に記載の組
成を有する接着剤を用意し、T剥離強度を測定した。Examples 7 to 9 In the same manner as in Example 1, adhesives having the compositions shown in Table 3 were prepared, and the T-peel strength was measured.
その結果は第3表の通りてあつた。尚、共重合ナイロン
及びポリテトラフロロエチレンは実施例1と同じものを
、ナイロン12は実施例2と同じものを夫々用いた。The results were as shown in Table 3. The same copolymerized nylon and polytetrafluoroethylene as in Example 1 were used, and the same as in Example 2 was used as nylon 12.
Claims (1)
ロロエチレンが1〜20重量部混合されてなることを特
徴とするホットメルト接着剤組成物。 2 ポリテトラフロロエチレンが微粒子でである第1項
記載の組成物。Claims: 1. A hot melt adhesive composition comprising 1 to 20 parts by weight of polytetrafluoroethylene mixed with 100 parts by weight of a nylon polymer. 2. The composition according to item 1, wherein the polytetrafluoroethylene is in the form of fine particles.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9481779A JPS6045672B2 (en) | 1979-07-24 | 1979-07-24 | hot melt adhesive composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9481779A JPS6045672B2 (en) | 1979-07-24 | 1979-07-24 | hot melt adhesive composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5618673A JPS5618673A (en) | 1981-02-21 |
| JPS6045672B2 true JPS6045672B2 (en) | 1985-10-11 |
Family
ID=14120601
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9481779A Expired JPS6045672B2 (en) | 1979-07-24 | 1979-07-24 | hot melt adhesive composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6045672B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58189273A (en) * | 1982-04-28 | 1983-11-04 | Kao Corp | Composition for foamed hot-melt adhesive |
-
1979
- 1979-07-24 JP JP9481779A patent/JPS6045672B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5618673A (en) | 1981-02-21 |
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