JPS61188480A - Release agent - Google Patents

Release agent

Info

Publication number
JPS61188480A
JPS61188480A JP2887485A JP2887485A JPS61188480A JP S61188480 A JPS61188480 A JP S61188480A JP 2887485 A JP2887485 A JP 2887485A JP 2887485 A JP2887485 A JP 2887485A JP S61188480 A JPS61188480 A JP S61188480A
Authority
JP
Japan
Prior art keywords
glass
release agent
base material
adhesive
iron
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.)
Pending
Application number
JP2887485A
Other languages
Japanese (ja)
Inventor
Takashi Saijo
西城 隆
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.)
SHOKO KAGAKU KENKYUSHO KK
Original Assignee
SHOKO KAGAKU KENKYUSHO KK
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 SHOKO KAGAKU KENKYUSHO KK filed Critical SHOKO KAGAKU KENKYUSHO KK
Priority to JP2887485A priority Critical patent/JPS61188480A/en
Publication of JPS61188480A publication Critical patent/JPS61188480A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a release agent enabling a rapid peeling without damage to a base material, which comprises an ester of a specific compound with an alcohol. CONSTITUTION:A release agent comprising an ester of a compound of the formula CH3(CH2)nCOOH and/or an adduct of CH3(CH2)nCOOH with R-OH (wherein n>=4; R is CxH2x+1; and x is 1-31 provided that, when x>=3, R may include isomers), with an alcohol of the formula CyH2y+1OH (wherein y>=1, provided that, when y>=3, the alcohol may include isomers).

Description

【発明の詳細な説明】 近年生活環境の多様化に伴なう接着剤の進歩は目覚しい
ものがある。従来の接着剤に依る接合固定は被接合物の
材質、接合能力に依り大きな規制を受けていた。
DETAILED DESCRIPTION OF THE INVENTION In recent years, advances in adhesives have been remarkable as living environments have become more diverse. Conventional bonding and fixing using adhesives has been subject to significant restrictions depending on the material and bonding ability of the objects to be bonded.

しかしながら現在の接着剤の進歩は被接着物(以下基材
と言う)の材質の種を問う事なく、又接着能力も大巾に
進歩して従来の規制を脱したかんがある。接着能力特に
、接着力の向上と接着時間の短縮化は金属、ガラス、セ
ラミックス、プラスチックスの活用分野を新規に開拓し
たと言っても過言ではない。本来接着剤は物と物との接
合固定が主目的である為に、剥離しがたい様に調整され
ている。
However, the current advances in adhesives have made it possible to overcome the conventional regulations by making great progress in bonding ability, regardless of the type of material of the object to be bonded (hereinafter referred to as the base material). It is no exaggeration to say that the improved adhesive strength and shortened bonding time have opened up new fields of application for metals, glass, ceramics, and plastics. Since the primary purpose of adhesives is to bond things together, they are designed to be difficult to peel off.

しかしながら金属、ガラス、セラミックス、プラスチッ
クスに於ける新規の活用分野での接着剤に対する要求は
、強力なる瞬間接着能と共に剥離の容易性をも要求して
いるのである。
However, new applications for adhesives in metals, glass, ceramics, and plastics require strong instant adhesive properties as well as ease of peeling.

この相反する要求に答えうる接着剤を開発する事は不可
能であろう。それ故剥離剤が新たに必要とされるのであ
る。瞬間接着剤は金属、ガラス。
It would be impossible to develop an adhesive that could meet these conflicting demands. Therefore, a new release agent is required. Instant adhesive is for metal and glass.

セラミックス、プラスチックスを重ねて切断する場合の
仮トメ剤として近年需要が多い。又これらの素材の研磨
に於ける仮固定剤としても使用されている。
In recent years, it has been in high demand as a temporary toning agent when cutting ceramics and plastics in layers. It is also used as a temporary fixing agent in polishing these materials.

しかしながらいずれの場合に於いても切断、研磨が終了
した時点では剥離されるのである。現在この剥離工程で
使用されている物は酢酸エチルやケトン系(主としてア
セトン)溶剤である。これら溶剤に依る剥離剤は接着膜
を溶解して剥離する機構である。故に剥離には1昼夜の
浸漬を要する。
However, in either case, it is peeled off when cutting and polishing are completed. Currently, ethyl acetate and ketone (mainly acetone) solvents are used in this stripping process. These solvent-based release agents have a mechanism of dissolving and peeling off the adhesive film. Therefore, peeling requires soaking for one day and night.

この長時間の浸漬は接着膜を溶解するだけにとどまらず
、基材がプラスチックスの場合には膨潤。
This long immersion not only dissolves the adhesive film, but also causes it to swell if the base material is plastic.

溶解をきたす事になる。This will cause dissolution.

又安全衛生面よりみても酢酸エチルやケトン系溶剤の使
用は好ましいものではなく、火災の危険性をもはらんで
いる。感圧接着剤特に接着両面テープの剥離に於いては
、接着テープ下面の接着力が強力になる為に基材の破損
をきたしがちである。
Also, from the standpoint of safety and hygiene, the use of ethyl acetate and ketone solvents is not desirable, and there is a risk of fire. When peeling pressure-sensitive adhesives, especially adhesive double-sided tapes, the adhesive force on the underside of the adhesive tape becomes strong, which tends to cause damage to the base material.

それ故剥離には最大の注意を払いながら溶剤を基材と接
着テープ下面との間に含浸させて剥離する事になるが、
基材が樹脂やプリント合板の場合には樹脂表面の白化、
膨潤、溶解及び基材破壊をきたす事になる。
Therefore, it is necessary to impregnate the space between the base material and the bottom surface of the adhesive tape with a solvent and peel it off, paying the utmost attention to peeling.
If the base material is resin or printed plywood, whitening of the resin surface,
This will cause swelling, dissolution and destruction of the base material.

以上の如く現在使用されている剥離剤では、溶剤を使用
する為に接着膜の溶解だけに留まらず基材の破損、安全
衛生面での問題、並びに火災の危険性をはらむのである
。又本来の剥離能を得るには長時間を要する。
As described above, the release agents currently in use use solvents, which not only dissolve the adhesive film, but also cause damage to the base material, health and safety issues, and the risk of fire. Moreover, it takes a long time to obtain the original peeling ability.

本発明に依る剥離剤を用いれば、従来の剥離剤に見られ
た欠点を危惧する事なく、短時間に剥離が可能となるの
′である。
By using the stripping agent according to the present invention, stripping can be performed in a short time without worrying about the drawbacks seen in conventional stripping agents.

CH3(CH2)nCOOHはn≧4(nは整数)であ
り、CH3(CH2)nC0OHのR−OH付加物に於
けるRはCxH2x+1 (x = 1〜31の整数)
にして、X≧3は異性体を含むものである。CyH2,
+10Hで表わされるアルコールはy≧1(yは整数)
であり、y≧3は異性体を含むものとする。このCH3
(CH2>nC0OH及び/又はCHa(CHz)HC
OOHのR−OH付加物とアルコールを少なくとも1種
以上含有する物とのエステルからなる剥離剤は接着膜を
溶解する事なく、基材と接着膜との間に浸透して離型層
を形成する事に依り、短時間に剥離を可能とする。しか
も従来の剥離剤の如き浸漬は不要で、剥離したい部分(
こ少量塗布する事に依り目的は達せられるのである。又
本発明に依る剥離剤は金属、ガラス、セラミックス、プ
ラスチックスの基材を損う事なく、安全衛生面及び火災
の危険性に対する危惧から解放されるのである。
CH3(CH2)nCOOH is n≧4 (n is an integer), and R in the R-OH adduct of CH3(CH2)nCOOH is CxH2x+1 (x = integer from 1 to 31)
and X≧3 includes isomers. CyH2,
Alcohol represented by +10H is y≧1 (y is an integer)
and y≧3 includes isomers. This CH3
(CH2>nC0OH and/or CHa(CHz)HC
A release agent made of an ester of an R-OH adduct of OOH and a product containing at least one alcohol does not dissolve the adhesive film, but penetrates between the base material and the adhesive film to form a release layer. By doing so, it is possible to peel off in a short time. What's more, there is no need for immersion like with conventional removers, and the area you want to remove (
The purpose can be achieved by applying a small amount. Furthermore, the stripping agent according to the present invention does not damage the base materials of metals, glass, ceramics, and plastics, and is free from concerns regarding safety, health, and fire hazards.

実施例1 基材はアルミニウム、鉄、ガラス、ポリカーボネイト、
セラミックスの板を使用す。
Example 1 Base materials are aluminum, iron, glass, polycarbonate,
Use a ceramic plate.

板の寸法は1 am X 5 cm (以下基材寸法は
同じとする)っシアノアクリレート系瞬間接着剤を使用
して上記基材の同種間の接着をする。なお接着面積は1
d(以下接着面積は同じとする)である。
The dimensions of the board are 1 am x 5 cm (hereinafter the dimensions of the substrates are the same). Cyanoacrylate instant adhesives are used to adhere the same types of substrates. The adhesive area is 1
d (hereinafter the adhesive area is the same).

剥離テストは接着後24時間経過した物を使用す。For the peel test, use the product 24 hours after adhesion.

剥離剤は2−メチル−ヘキサン酸とC16H330Hと
のエステルを使用す。各基材の接合隣接部4面に剥離剤
を塗布す。塗布後者基材の剥離に要した時間は以下の如
きものである。アルミニウム20分間、鉄15分間、ガ
ラス5分間、ポリカーボネイト30分間、セラミックス
5分間。基材の損傷はなかった。
As a stripping agent, an ester of 2-methyl-hexanoic acid and C16H330H is used. Apply a release agent to the four adjacent surfaces of each base material to be joined. The time required to peel off the coated substrate is as follows. Aluminum for 20 minutes, iron for 15 minutes, glass for 5 minutes, polycarbonate for 30 minutes, ceramics for 5 minutes. There was no damage to the base material.

実施例2 基材は鉄とセラミックス、ガラスとポリカーボネイトを
用いてシアノアクリレート系瞬間接着剤で接着す。
Example 2 The base materials are iron and ceramics, glass and polycarbonate, and are bonded together using a cyanoacrylate instant adhesive.

接着後24時間経過してから剥離テストに供す。A peel test was performed 24 hours after adhesion.

剥離剤は3−エチル−ヘキサン酸とCl8H370Hと
のエステルを使用す。各基材の接合隣接部4面に剥離剤
を塗布す。塗布後剥離に要した時間は鉄とセラミックス
の接合体で7分間、ガラスとポリカーボネイトの接合体
で7分80秒間である。基材の損傷はなかった。
As a stripping agent, an ester of 3-ethyl-hexanoic acid and Cl8H370H is used. Apply a release agent to the four adjacent surfaces of each base material to be joined. The time required for peeling after application was 7 minutes for the bonded body of iron and ceramics, and 7 minutes and 80 seconds for the bonded body of glass and polycarbonate. There was no damage to the base material.

実施例3 基材は鉄と鉄、ガラスとガラス、ガラスとポリカーボネ
イトを用いてシアノアクリレート系瞬間接着剤で接着す
Example 3 The base materials are iron to iron, glass to glass, and glass to polycarbonate, and are bonded together using a cyanoacrylate instant adhesive.

接着後24時間経過してから剥離テストに供す。A peel test was performed 24 hours after adhesion.

剥離剤は2−メチル−ヘキサン酸とC16H330H及
びCl8H370Hとのエステルを使用す。各基材の接
合隣接部4面に剥離剤を塗布す。塗布後剥離に要した時
間は鉄と鉄で30秒間、ガラスとガラスで20秒間、ガ
ラスとポリカーボネイトで1分間である。基材の損傷は
なかった。
As a stripping agent, esters of 2-methyl-hexanoic acid and C16H330H and Cl8H370H are used. Apply a release agent to the four adjacent surfaces of each base material to be joined. The time required for peeling after application was 30 seconds for iron and iron, 20 seconds for glass and glass, and 1 minute for glass and polycarbonate. There was no damage to the base material.

実施例4 基材はアルミニウムとプリント合板、接着剤は合成ゴム
系の接着両面テープを使用、接着後24時間経過した物
を剥離テストに供す。剥離剤は2−プロピル−ヘキサン
酸とCl2H250H及びC17H350Hとのエステ
ルを使用す。
Example 4 The base material was aluminum and printed plywood, and the adhesive was a synthetic rubber adhesive double-sided tape. After 24 hours of adhesion, the product was subjected to a peel test. As a stripping agent, esters of 2-propyl-hexanoic acid and Cl2H250H and C17H350H are used.

接合隣接部4面に剥離剤を塗布す。塗布機剥離に要した
時間はアルミ側で30秒、プリント合板側で1分間であ
った。なお、プリント合板面の損傷はなかった。
Apply a release agent to the four surfaces adjacent to the joint. The time required for the coating machine to peel off was 30 seconds on the aluminum side and 1 minute on the printed plywood side. There was no damage to the printed plywood surface.

実施例5 基材は鉄と鉄、ガラスとガラスを用いてシアノアクリレ
ート系瞬間接着剤で接着す。接着後24時間経過してか
ら剥離テストに供す。
Example 5 The base materials are iron-to-iron and glass-to-glass, which are bonded together using a cyanoacrylate instant adhesive. A peel test was performed 24 hours after adhesion.

剥離剤はCH3(CH2) lr、 C0OHとC4H
90Hとのエステルを使用す。なおこのエステルは20
℃以下テは少しゲル化するので、40’Cに加熱してか
ら使用した。接合隣接部4面に剥離剤を塗布す。剥離に
要した時間は鉄と鉄で25分間、ガラスとガラスで10
分間であった。基材の損傷はなかった。
Stripping agents are CH3 (CH2) lr, C0OH and C4H
An ester with 90H is used. This ester is 20
Since it gels slightly at temperatures below 40°C, it was heated to 40'C before use. Apply a release agent to the four surfaces adjacent to the joint. The time required for peeling was 25 minutes for iron to iron and 10 minutes for glass to glass.
It was a minute. There was no damage to the base material.

実施例6 基材は鉄とガラス、アルミニウムとポリカーボネイトを
用いてシアノアクリレート系接着剤で接着す。接着後2
4時間経過したものを剥離テストに供す。
Example 6 The base materials are iron and glass, aluminum and polycarbonate, and are bonded together using a cyanoacrylate adhesive. After gluing 2
After 4 hours have passed, the sample is subjected to a peel test.

剥離剤はCH3(CH2) 16C00HとCH3(C
H2)14COOHとが重量比で4:1よりなる混合比
とC3H7OHとのエステルを使用す。
The release agent is CH3 (CH2) 16C00H and CH3 (C
H2) An ester of C3H7OH and 14COOH in a mixing ratio of 4:1 by weight is used.

接合隣接部4面に剥離剤を塗布す。剥離に要した時間は
鉄とガラスで7分間、アルミニウムとポリカーボネイト
で15分間を要した。なおこのエステルは20℃以下で
は少しゲル化するので、40℃に加熱した物を使用す。
Apply a release agent to the four surfaces adjacent to the joint. The time required for peeling was 7 minutes for iron and glass, and 15 minutes for aluminum and polycarbonate. Note that this ester slightly gels at temperatures below 20°C, so use one heated to 40°C.

基材の損傷はなかった0 実施例7 基材はガラスとガラス、鉄とアルミニラムラ用いてシア
ノアクリレート系瞬間接着剤で接着す。
There was no damage to the base material.0 Example 7 The base materials were glass and glass, iron and aluminum Ramura, and were bonded together using a cyanoacrylate instant adhesive.

接着後24時間経過したものをテストに供す。Tests are conducted 24 hours after adhesion.

剥離剤は下記のけ)、(ロ)、(ハ)の3種を重量比に
1:1で混合した物を使用す。
The release agent used is a mixture of the following three types (a), (b), and (c) in a weight ratio of 1:1.

(イ) 3−エチル−ヘキサン酸とCl8H370Hと
のエステル (CI)  CH3(CH2)20COOHとC4H9
0HとのエステルM  CI(3(CH2)16COO
HとC4H90Hとノエステル接合隣接部4面に剥離剤
を塗布す。
(a) Ester of 3-ethyl-hexanoic acid and Cl8H370H (CI) CH3(CH2)20COOH and C4H9
Ester M CI (3(CH2)16COO with 0H
Apply a release agent to the 4 surfaces adjacent to H, C4H90H, and Noester bond.

剥離に要した時間はガラスとガラスで1分間、鉄とアル
ミニウムで3分間であった。
The time required for peeling was 1 minute for glass and glass, and 3 minutes for iron and aluminum.

なおこの剥離剤は20′C以下でもゲル化はなかった。This release agent did not gel even at temperatures below 20'C.

又基材の損傷もなかった。Moreover, there was no damage to the base material.

Claims (4)

【特許請求の範囲】[Claims] (1)CH_3(CH_2)_nCOOH及び/又はC
H_3(CH_2)_nCOOHのR−OH付加物とア
ルコールを少なくとも1種以上含有する物とのエステル
からなる剥離剤。
(1) CH_3(CH_2)_nCOOH and/or C
A stripping agent consisting of an ester of an R-OH adduct of H_3(CH_2)_nCOOH and a product containing at least one type of alcohol.
(2)CH_3(CH_2)_nCOOHはn≧4の整
数である処の特許請求の範囲第1項記載の剥離剤。
(2) The release agent according to claim 1, wherein CH_3(CH_2)_nCOOH is an integer of n≧4.
(3)R−OHはRがCxH_2_x_+_1で表わさ
れるアルコールで、x=1〜31の整数であり、x≧3
は異性体を含む処の特許請求の範囲第1項記載の剥離剤
(3) R-OH is an alcohol in which R is represented by CxH_2_x_+_1, x = an integer from 1 to 31, and x≧3
The stripping agent according to claim 1, wherein contains an isomer.
(4)アルコールはCyH_2_y_+_1OH(y≧
1の整数)であり、y≧3は異性体を含む処の特許請求
の範囲第1項記載の剥離剤。
(4) Alcohol is CyH_2_y_+_1OH (y≧
1), and y≧3 includes isomers.
JP2887485A 1985-02-15 1985-02-15 Release agent Pending JPS61188480A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2887485A JPS61188480A (en) 1985-02-15 1985-02-15 Release agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2887485A JPS61188480A (en) 1985-02-15 1985-02-15 Release agent

Publications (1)

Publication Number Publication Date
JPS61188480A true JPS61188480A (en) 1986-08-22

Family

ID=12260524

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2887485A Pending JPS61188480A (en) 1985-02-15 1985-02-15 Release agent

Country Status (1)

Country Link
JP (1) JPS61188480A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988006613A1 (en) * 1987-03-02 1988-09-07 Nippon Carbide Kogyo Kabushiki Kaisha Film releasing agent
KR100517431B1 (en) * 2002-11-27 2005-09-29 한국타이어 주식회사 Peeling agent composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988006613A1 (en) * 1987-03-02 1988-09-07 Nippon Carbide Kogyo Kabushiki Kaisha Film releasing agent
KR100517431B1 (en) * 2002-11-27 2005-09-29 한국타이어 주식회사 Peeling agent composition

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