JPS61112610A - Release agent - Google Patents
Release agentInfo
- Publication number
- JPS61112610A JPS61112610A JP23561584A JP23561584A JPS61112610A JP S61112610 A JPS61112610 A JP S61112610A JP 23561584 A JP23561584 A JP 23561584A JP 23561584 A JP23561584 A JP 23561584A JP S61112610 A JPS61112610 A JP S61112610A
- Authority
- JP
- Japan
- Prior art keywords
- mold release
- release agent
- repeated unit
- halogen
- polyether
- 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
Links
Landscapes
- Polyethers (AREA)
Abstract
Description
【発明の詳細な説明】
し産業上の利用分野コ
本発明は、離型剤に関し、更に詳しくは合成樹脂又はゴ
ム(以下、単に「合成樹脂」という。なおそれらの発泡
体をも含む。)等の高分子物質の成型物製造の際に使用
される含ハロゲンポリエーテルを主成分とする離型剤に
関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a mold release agent, and more specifically to synthetic resins or rubbers (hereinafter simply referred to as "synthetic resins"; foams thereof are also included). This invention relates to a mold release agent whose main component is a halogen-containing polyether, which is used in the production of molded products of polymeric substances such as polyethers.
[従来技術]
従来、例えばノリコンオイル、鉱物油、パラフィンワッ
クス、脂肪酸誘導体、グリコール等の天然若しくは合成
化合物や、タルク、マイカ等の無機物等が高分子物質の
成型の際の離型剤として使用されている。[Prior art] Conventionally, natural or synthetic compounds such as Noricon oil, mineral oil, paraffin wax, fatty acid derivatives, and glycol, as well as inorganic substances such as talc and mica, have been used as mold release agents when molding polymeric materials. has been done.
一般にこれらの離型剤は被成型物か導入される以前に型
に塗布され、離型寿命の短い場合には毎回導入前に塗布
されるのが@通である。ノリコンオイルは離型性が良好
なため最も普遍的に使用されている離型剤であるが、こ
の場合でらウレタンやエポキノ樹脂のように接着性の強
い物に使用する場合は酸化珪素の微粉末等を添加して離
型剤膜の強度を改良したものをしかも多量に塗布する必
要がある。この様に多量に塗布することは離型剤の被成
型体への移行を招き、成型物表面の後処理、例えば塗装
や接着処理が不可能になるばかりてなく、コスト面から
も望ましいことではない。さらにノリコン浦はプラスチ
ックスの表面で匍fillする現象があり、電気部品の
成型加工に用いる時には接点部の導通不良を起こすこと
が多かった。Generally, these mold release agents are applied to the mold before the molded article is introduced, and if the mold release life is short, it is customary to apply them before each introduction. Noricon oil is the most commonly used mold release agent due to its good mold release properties, but when used for materials with strong adhesive properties such as urethane and epochino resin, it is necessary to use silicon oxide. It is necessary to improve the strength of the release agent film by adding fine powder or the like, and to apply it in large quantities. Applying such a large amount causes the release agent to migrate to the molded object, which not only makes it impossible to perform post-treatments on the surface of the molded object, such as painting or adhesive treatment, but also makes it undesirable from a cost perspective. do not have. Furthermore, Norikonura has a phenomenon in which it fills on the surface of plastics, and when used in the molding process of electrical parts, it often causes poor conduction at the contact portion.
さらに、多量に離型剤を塗布する事により一つの金型で
成型加工を続けると、離型剤のカスや成型物のカス等が
金型表面にたまり、金型をたびたび洗滌する必要が生し
成型加工の能率を低下させる原因になっていた。Furthermore, if molding is continued in one mold by applying a large amount of mold release agent, mold release agent residue and molded product debris will accumulate on the mold surface, making it necessary to wash the mold frequently. This caused a decrease in the efficiency of the molding process.
フッ素化合物は低表面エネルギーを宵して居り、そのも
の自体でら離型性を有する事が知られており、すでにパ
ーフルオロアルキル基ををするアルコールのりん酸エス
テルとノリコン油等を配合した離型性のよい離型剤が得
られている(特公昭53−23271号公報参照)。Fluorine compounds have low surface energy and are known to have mold releasability by themselves, and mold release methods have already been developed by combining phosphoric acid esters of alcohols containing perfluoroalkyl groups with Noricon oil, etc. A mold release agent with good properties has been obtained (see Japanese Patent Publication No. 53-23271).
しかし、パーフルオロアルキル基を有するアルコールの
りん酸エステルを含有する離型剤は、りん酸エステルが
反応性の官能基を持つために、例えば発泡ポリウレタン
の様に反応性の巷を有する樹脂の成型加工の際には一部
が樹脂の表面と反応し表面が荒れたりする場合があると
いう欠点がある。又、これ等パーフルオロアルキル基を
含有するりん酸エステルは耐熱性が充分でなく、高温高
熱下での長時間にわたる成型加工を行う場合、炭化分解
を起こし金型上にカスがたまる事が多かった。However, mold release agents containing phosphate esters of alcohols having perfluoroalkyl groups are used for molding resins with a reactive range, such as foamed polyurethane, because the phosphate esters have reactive functional groups. There is a drawback that during processing, a part of the resin may react with the surface of the resin, causing the surface to become rough. In addition, these phosphoric acid esters containing perfluoroalkyl groups do not have sufficient heat resistance, and when molding is performed at high temperatures for a long period of time, carbonization decomposition occurs and scum often accumulates on the mold. Ta.
[発明の目的]
本発明の目的は、蒸気圧、表面張力が低く、熱分解開始
温度が高く、熱安定性の良好であり、優れた離型性と金
型汚れが少ない離型剤を提供することにある。[Object of the invention] The object of the present invention is to provide a mold release agent that has low vapor pressure, low surface tension, high thermal decomposition initiation temperature, good thermal stability, excellent mold releasability, and little mold staining. It's about doing.
し発明の構成〕
本発明の要旨・は、式:
%式%)
[式中、a、 b、 c、 dSeおよび「はそれぞれ
0または正の整数であって、2≦a+b+c+d+e+
f≦200およびa+c+d+f≧1を満足する数であ
る。]で示されるくり返し単位を有する含ハロゲンポリ
エーテルを主成分とする離型剤に存する。[Configuration of the Invention] The gist of the present invention is the formula: %Formula%) [In the formula, a, b, c, dSe and " are each 0 or a positive integer, and 2≦a+b+c+d+e+
The number satisfies f≦200 and a+c+d+f≧1. The release agent consists of a halogen-containing polyether having a repeating unit represented by the following formula.
なお、式(r)中、各括弧内にくり返し単位の分子中で
の配列は任意であり、必ずしら上記の順に配列している
ことを怠味するらのではない。また、X、YおよびZの
それぞれは、同一分子中の異なる繰り返し単位において
異なる意義を有していてらよい。たとえば、ある繰り返
し単位ではZがフッ素であるが、池の繰り返し単位では
Zが塩素であってらよい。In formula (r), the arrangement of the repeating units in each parenthesis in the molecule is arbitrary, and it is not mandatory to arrange them in the above order. Furthermore, each of X, Y and Z may have different meanings in different repeating units within the same molecule. For example, in some repeating units Z may be fluorine, while in the pond repeating unit Z may be chlorine.
本発明で用いられる含ハロゲンポリエーテルは、新規化
合物である。これらの内、qおよびrが0であるポリエ
ーテルおよびその製法は、特願昭58−251069号
に記載され、XSYおよびZがフッ素であるポリエーテ
ルおよびその製法は、特願昭59−58877号に記載
され、さらにX1YおよびZの内生なくとも1つが塩素
であるポリエーテルおよびその製法は、昭和59年11
月7日出願の特許出願(発明の名称「新規含ハロゲンポ
リエーテルおよびその製法と用途」)に記載されている
。The halogen-containing polyether used in the present invention is a new compound. Among these, polyethers in which q and r are 0 and their manufacturing method are described in Japanese Patent Application No. 58-251069, and polyethers in which XSY and Z are fluorine and their manufacturing method are described in Japanese Patent Application No. 59-58877. Further, the polyether in which at least one of X1Y and Z is chlorine and the method for producing the same are described in November 1982.
It is described in a patent application filed on May 7th (title of invention: "Novel halogen-containing polyether and its manufacturing method and uses").
これらポリエーテルの製法を簡単に説明する。The manufacturing method of these polyethers will be briefly explained.
qおよびrが0であるポリエーテルは、2.2.3゜3
−テトラフルオロオキセクンを、一般には開始剤(たと
えば、ハロゲン化アルカリ金届または強いルイス酸性を
示す化合物)の存在下に開環重合させることにより製造
することができる。The polyether in which q and r are 0 is 2.2.3°3
-Tetrafluorooxecune can be prepared by ring-opening polymerization, generally in the presence of an initiator (for example, an alkali metal halide or a compound exhibiting strong Lewis acidity).
qおよびrの少なくとも一方が0でないポリエーテルは
、先に得られたqおよびrが0であるポリエーテルをフ
ッ素化および/または塩素化することにより容易に製造
することができる。A polyether in which at least one of q and r is not 0 can be easily produced by fluorinating and/or chlorinating the previously obtained polyether in which q and r are 0.
本発明で用いる含ハロゲンポリエーテルは、直鎖状のポ
リエーテルであるため、既知の分岐状含ハロゲンポリエ
ーテル、たとえば式。Since the halogen-containing polyether used in the present invention is a linear polyether, it is a known branched halogen-containing polyether, for example, the formula.
F i
−(CF CP to)n−(CF to)m−または
F3
■
−(CFCF、0)n−
で示される繰り返し単位を有する化合物および式: C
e(CF rc F Cl2)IIC+2で示される化
合物に比較すると、同一粘度の化合物同志を比べた場合
、本発明の含ハロゲンポリエーテルの方が、蒸気圧が低
く、温度変化により粘度変化が少なく、かつ耐薬品性お
よび耐熱性が優れでいる。Compounds having a repeating unit represented by F i -(CF CP to) n- (CF to) m- or F3 ■ - (CFCF, 0) n- and formula: C
Compared to the compound represented by e(CF rc F Cl2) IIC+2, when comparing compounds with the same viscosity, the halogen-containing polyether of the present invention has a lower vapor pressure, less viscosity change due to temperature change, It also has excellent chemical resistance and heat resistance.
[発明の効果]
本発明の離型剤は、蒸気圧及び表面張力が低く、熱分解
開始温度が高いので熱安定性が優れている。[Effects of the Invention] The mold release agent of the present invention has low vapor pressure and surface tension, and has a high thermal decomposition initiation temperature, so it has excellent thermal stability.
ポリウレタンの成型加工に用いて乙、表面が荒れること
かなく、電気部品の成型加工の場合に接点部の導通不良
を起こさない。When used in the molding process of polyurethane, the surface will not become rough and will not cause poor conductivity at the contact points when molding electrical parts.
[実施例コ
次に実施例および比較例を示し、本発明を具体的に説明
する。[Example] Next, Examples and Comparative Examples will be shown to specifically explain the present invention.
実施例1〜4および比較例1〜3
[試験方法]
(1,4cxφX深さ2c++のアルミニュウム型上に
表に示した離型剤を含む組成物(各種離型剤の2%トリ
クロロトリフ0ロエタン溶液)を刷毛塗り風乾する。次
いで、下記A液およびB液をハンドミキサーにより15
00rpmで攪拌混合し、直ちに上記アルミニュウム型
上に流し込み、25℃で5分間発泡硬化させた後、引張
試験機(引張速度25H/win)を用いて接着強度を
求め、離型性能を測定した。Examples 1 to 4 and Comparative Examples 1 to 3 [Test method] (A composition containing the mold release agent shown in the table on an aluminum mold of 1,4 c x φ Solution) was applied with a brush and air-dried.Then, the following solutions A and B were mixed with a hand mixer for 15 minutes.
The mixture was stirred and mixed at 00 rpm, immediately poured into the aluminum mold, and foamed and cured at 25° C. for 5 minutes. The adhesive strength was determined using a tensile tester (tensile speed 25 H/win) and the mold release performance was measured.
A液
・ポリオールPOP31−28 100 重量部
「日本ウレタン(株)]
・ポリオールEG/DIEP I 2 ノ
![日本ウレタン(株)ト
ノリコーノし5302 1 、0 ノ’5日本
ユニカー(抹)]
・ポリアミノDabco O、8〃・
ボ’J7ミンDBTDL O,01!/・ト
リクロロモノフルオロエタン
DF−II lol/[ダイキン工
業(株)]
B液
イソノアネー)MDi−CL 44.711[日本
ウレタン(株)]
結果を、次表に示す。Part A - Polyol POP31-28 100 parts by weight "Nippon Urethane Co., Ltd." - Polyol EG/DIEP I 2 No! [Nippon Urethane Co., Ltd. Tonorikonoshi 5302 1,0 No'5 Nippon Unicar (Merger)] - Polyamino Dabco O, 8〃・
Bo'J7 Min DBTDL O,01! / Trichloromonofluoroethane DF-II lol/[Daikin Industries, Ltd.] B liquid isonoane) MDi-CL 44.711 [Nippon Urethane Co., Ltd.] The results are shown in the following table.
実施例で用いたポリウレタン成型物の表面は非常にきれ
いであった。The surface of the polyurethane molded product used in the examples was very clean.
Claims (1)
_2CF_2O)b−(CCl_2CF_2CF_2O
)c−(CHFCF_2CF_2O)d−(CFClC
F_2CF_2O)e−(CF_2CF_2CF_2O
)f−[式中、a、b、c、d、eおよびfはそれぞれ
0または正の整数であって、2≦a+b+c+d+e+
f≦200およびa+c+d+f≧1を満足する数であ
る。]で示されるくり返し単位を有する含ハロゲンポリ
エーテルを主成分とする離型剤。(1) Formula: -(CH_2CF_2CF_2O)a-(CHClCF
_2CF_2O)b-(CCl_2CF_2CF_2O
)c-(CHFCF_2CF_2O)d-(CFClC
F_2CF_2O)e-(CF_2CF_2CF_2O
)f- [where a, b, c, d, e and f are each 0 or a positive integer, and 2≦a+b+c+d+e+
The number satisfies f≦200 and a+c+d+f≧1. ] A mold release agent whose main component is a halogen-containing polyether having a repeating unit.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23561584A JPS61112610A (en) | 1984-11-07 | 1984-11-07 | Release agent |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23561584A JPS61112610A (en) | 1984-11-07 | 1984-11-07 | Release agent |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61112610A true JPS61112610A (en) | 1986-05-30 |
JPH039848B2 JPH039848B2 (en) | 1991-02-12 |
Family
ID=16988628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23561584A Granted JPS61112610A (en) | 1984-11-07 | 1984-11-07 | Release agent |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61112610A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993022121A1 (en) * | 1992-04-28 | 1993-11-11 | Daikin Industries, Ltd. | Parting agent |
-
1984
- 1984-11-07 JP JP23561584A patent/JPS61112610A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993022121A1 (en) * | 1992-04-28 | 1993-11-11 | Daikin Industries, Ltd. | Parting agent |
US5525150A (en) * | 1992-04-28 | 1996-06-11 | Daikin Industries Ltd. | Mold release agent |
Also Published As
Publication number | Publication date |
---|---|
JPH039848B2 (en) | 1991-02-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |