JPS58120661A - Resin composition for releasing materials - Google Patents
Resin composition for releasing materialsInfo
- Publication number
- JPS58120661A JPS58120661A JP423582A JP423582A JPS58120661A JP S58120661 A JPS58120661 A JP S58120661A JP 423582 A JP423582 A JP 423582A JP 423582 A JP423582 A JP 423582A JP S58120661 A JPS58120661 A JP S58120661A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- vinyl
- ethylene
- weight
- vinyl acetate
- 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
- Compositions Of Macromolecular Compounds (AREA)
- Adhesive Tapes (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は剥離性の良好な剥離材料、特に剥離紙用樹脂組
成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a release material with good releasability, particularly to a resin composition for release paper.
従来、紙材、プラスチックフィルム等の基材にシリコー
ン、塩化ビニル樹脂、塩化ビニリデン−塩化ビニル共重
合体樹脂、ポリエチレン等の樹脂を塗布成層して剥離材
料の製造が行なわれている。ところがシリコーン系樹1
1mを用いた場合は紙材にシリコーン樹Bイが浸壇する
ため予め紙材に例えばポリエチレン樹脂と塗工するなど
アンカーコートを行なった後シリコーン&kを塗布する
方法が採用されているが、この方法は二工程を8委とす
るという欠点がある。また塩化ビニIし樹脂、ポリエチ
レン66B11などを用いる場合は対象物質に対する剥
離効果が少ないかまたは適用し得る範囲が狭いなどの欠
点がある。Conventionally, release materials have been manufactured by coating and layering resins such as silicone, vinyl chloride resin, vinylidene chloride-vinyl chloride copolymer resin, and polyethylene on base materials such as paper materials and plastic films. However, silicone tree 1
When using 1 m, the silicone resin is immersed in the paper material, so a method is used in which the paper material is coated with an anchor coat, such as polyethylene resin, and then silicone &k is applied. The method has the disadvantage of requiring 2 steps and 8 trials. Furthermore, when vinyl chloride I resin, polyethylene 66B11, or the like is used, there are drawbacks such as a poor peeling effect on the target substance or a narrow range of applicability.
本発明苔らはこのような欠点を解決すべく鋭意研究した
紹果、特定の七ツマー組成の酢酸ビニル、エチレンおよ
び官能基を有するビニル早麓体からなる共重合体エマl
レジ1ンあるいはその変性物と7ミノ樹脂及びシリコー
ン横側を特定比率で配合してなる組成物が剥離材料への
塗布工程を一工程にし、しかも対象物に対する剥離性に
も優れ、剥離材料用として極めて自゛効であることを見
出し本発明を完成するに至った。In order to solve these drawbacks, the present inventors have made intensive research to develop a copolymer emulsion consisting of vinyl acetate with a specific heptamer composition, ethylene, and a vinyl ester having a functional group.
A composition made by blending Resin 1 or its modified product, 7Mino resin, and silicone side in a specific ratio reduces the coating process to a release material in one step, and has excellent releasability to the target object, making it suitable for release materials. The present inventors have discovered that the method is extremely effective and have completed the present invention.
すなわち、本発明は(A)erP酸ビニIし、エテレン
および官能基を有するビニ4単量体の組成が重量比で7
0〜96:4〜29:1〜lOである共重合体エマルジ
ーンもしくはその変性物の20〜90重量%、0アミノ
樹脂M5〜40重瀘%、および0シリコ一ン樹脂5〜7
6N1%(いずれも固型分)を主成分とする剥離材料用
樹脂組成物である。That is, the present invention provides (A) erP acid vinyl I, and the composition of vinyl 4 monomer having ethylene and a functional group is 7 in weight ratio.
0-96:4-29:20-90% by weight of a copolymer emulgene or a modified product thereof, 0-96:4-29:1-10% by weight, 0-amino resin M5-40% by weight, and 5-7% silicone resin.
This is a resin composition for a release material whose main component is 6N1% (all solid content).
本発明に用いる酢酸ビニル、エチレンおよび官能基を有
するビニtL/皐重体からなる共重合体エマルジーンは
原料モノマーである酢酸ビニ?し、エチレン、官能基を
有するビニル単重体の組成比が重量比で70〜95:4
〜29:1〜10の共重合体もしくはその変性物であっ
て、この場合エチレンが29重量%を越えるかあるいは
官能基を儒するビニル単量体が13!瀘%未満であると
得られる剥離材料用樹脂組成物はブロッキングを起し易
く、剥離性にも劣り、またエチレンが4重量%未満ある
いは官能基を有するビニル単量体が10重量%を越える
と耐折性に劣り本発明による効果が#麹くなる。The copolymer emulgene made of vinyl acetate, ethylene, and a vinyl tL/carbon polymer having a functional group used in the present invention is made of vinyl acetate, which is a raw material monomer. The composition ratio of ethylene and a vinyl monomer having a functional group is 70 to 95:4 by weight.
-29: A copolymer of 1 to 10 or a modified product thereof, in which case the ethylene content exceeds 29% by weight or the vinyl monomer having a functional group contains 13! If the amount of ethylene is less than 4% by weight or the vinyl monomer having a functional group exceeds 10% by weight, the resulting resin composition for release materials will easily cause blocking and have poor peelability. The folding durability is poor and the effect of the present invention becomes #koji.
本発明における官能基を飼するビニル単量体としてはグ
リシジル基、力Iレボキシ?し基、スlシホン酸基、ヒ
ドロキシIし詔、アミド基、N−メチロールアミド基、
アIレコキシメチrレアミド基を有する単重体であり、
例えば、グリシジルメタクリレート、アクリーレ頷、メ
タクリIし酸、β−ヒドロキシエチルアクリレート、β
−ヒドロキシエチルメタアクリレート、アクリルアミド
、N−メチロールアクリルアミド、N−ブトキシメチI
レアクリIレアミド、ビニルスルホン酸等が挙げられる
。In the present invention, the vinyl monomer having a functional group includes a glycidyl group, a levoxy group, and a glycidyl group. Shi group, sulfonic acid group, hydroxyl sulfonic acid group, amide group, N-methylolamide group,
is a monomer having an I recoxymethyl r reamide group,
For example, glycidyl methacrylate, acrylic acid, methacrylic acid, β-hydroxyethyl acrylate, β
-Hydroxyethyl methacrylate, acrylamide, N-methylolacrylamide, N-butoxymethyI
Examples include rarecrylamide, vinyl sulfonic acid, and the like.
本発明に用いる酢酸ビニル、エチレン、官能基を何する
ビニル単量体からなる共重合体は、原料である酢酸ビニ
ル、エチレンおよび官能基を自するビニル単量体の合計
に対して、10重量%以内でプロピオン酸ビニル、バー
サチック酸ビニルなどのビニルエステル、メチルアクリ
レート、メチリレメタアクリレートなどの(メタ)アク
リ−し酸エステルなどの共重合可能なビニル単重体を共
重合変性した変性物でもよい。The copolymer consisting of vinyl acetate, ethylene, and a vinyl monomer having a functional group used in the present invention is 10% by weight based on the total of the raw materials vinyl acetate, ethylene, and a vinyl monomer having a functional group. It may be a modified product obtained by copolymerizing and modifying a vinyl monopolymer that can be copolymerized, such as vinyl esters such as vinyl propionate and vinyl versatate, and (meth)acrylic acid esters such as methyl acrylate and methyl methacrylate. .
本発明におけるアミノ樹脂とは例えばメラミン、ベンゾ
ゲ1アナ之ンなどのトリアジン系あるいは尿素などのア
ルデヒド縮金物を基体として遊離のメチロ−θ基の一部
あるいは全部がアルコキシ化されたものが使用される。The amino resin used in the present invention is, for example, one based on a triazine type such as melamine or benzogane-1-ananone, or an aldehyde condensate such as urea, in which part or all of the free methylo-θ groups are alkoxylated. .
またメチロ−rし基およびイミノ基を多く何しているア
ミノ樹脂が低温加熱の場合に有利である。アミノ樹脂硬
化触媒を用いるとさらに低温加熱で硬化することができ
より自゛利である。アミノ樹脂硬化触媒とはたとえばp
−トルエンスルホン酸、シ、つ酸などの遊離酸、それら
のアミン塩またはアンモニウム塩、あるいは酸無水物、
燐酸エステタレ、硫酸エステル、酸アミド、イミドジス
ーレホン酸、ニトリロス−レホン酸塩などの熱分解によ
り酸を生ずるものなどが挙げられる。In addition, amino resins containing a large number of methyl-r groups and imino groups are advantageous in the case of low-temperature heating. When an amino resin curing catalyst is used, curing can be performed by heating at a lower temperature, which is more convenient. The amino resin curing catalyst is, for example, p
- Free acids such as toluenesulfonic acid, silicic acid, fornic acid, their amine salts or ammonium salts, or acid anhydrides;
Examples include those that produce acids upon thermal decomposition, such as phosphoric acid esters, sulfuric esters, acid amides, imidodisulephonic acids, and nitrilos-lephonates.
本発明に用いられるシリコーン樹脂とは最も普通に使用
されている溶剤あるいはエマルシーンタイプのものであ
るが、通信は特にエマルシーンタイプが水系であるため
に省資諒あり、例えば5M−7270(固型分aoi凰
%、トーレシリコーン社品)等が挙げられる。これらの
シリコーン−B−は融媒として例えば5M−7271(
シリコーン動態用触媒、固型分40重量%:トーレシリ
コーン社品)を併用して用いることもできる。The silicone resin used in the present invention is of the most commonly used solvent or emulscene type, but especially for communication, the emulseen type is water-based, which saves resources.For example, 5M-7270 (solid resin) Examples include Type Min Aoi 凰%, Toray Silicone Co., Ltd. product), etc. These silicone-B- can be used as a melting medium such as 5M-7271 (
A silicone dynamic catalyst (solid content: 40% by weight, manufactured by Toray Silicone Co., Ltd.) may also be used in combination.
本発明の剥離材料用樹脂組成物は、前記のような特定上
ツマー比の酢酸ビニル、エチレンおよび官能基を有する
ビニル単重体からなる共重合体エマルジーンもしくはそ
の変性物20〜90重嵐%、盆形好ましくは40〜80
ム量%、アミノ樹脂5〜40惠處%、より好ましくは一
8〜86重鰍%、シリコーン樹脂5〜75重胤%、好ま
しくは8〜60重慮%(いずれも固型分)からなるもの
である。The resin composition for a release material of the present invention is a copolymer emulgene or a modified product thereof consisting of vinyl acetate, ethylene, and a vinyl monomer having a functional group having a specific Zimmer ratio of 20 to 90%. Shape preferably 40-80
Amino resin 5-40 weight%, more preferably 18-86 weight%, silicone resin 5-75 weight%, preferably 8-60 weight% (all solid content) It is something.
ここでエマルジーンもしくはその変性物が20重量%未
満であると、該fMBFi組成物中のシリコーン樹脂か
基材へ浸透し均一な塗工ができなくなり、また90重鷺
%を越えると該組成物を塗工して得られた剥離材料の剥
離性が低下する等本発明の効果が十分に待られないO
またシリコーン樹脂が5重量%未渦であると剥離性に劣
り、76重重%を越えると剥離材にシリコーン樹脂の浸
透が多くなり均一な塗工か得暗くなる。If Emulgene or its modified product is less than 20% by weight, the silicone resin in the fMBFi composition will penetrate into the base material and uniform coating will not be possible, and if it exceeds 90% by weight, the composition will be damaged. The effect of the present invention cannot be fully expected, as the releasability of the release material obtained by coating decreases.In addition, if the silicone resin is 5% by weight without swirling, the releasability is poor, and if it exceeds 76% by weight, the releasability is poor. The silicone resin penetrates into the release material more and the coating becomes uniform and dark.
また、アミノ樹脂が5重重%未満であると耐ブロッキン
グ性に劣り、40重量%を越えると塗被膜が硬くなり耐
折性が悪化する。Furthermore, if the amino resin content is less than 5% by weight, the blocking resistance will be poor, and if it exceeds 40% by weight, the coating will become hard and the folding durability will deteriorate.
本発明の剥離材料用樹脂組成物には必要に応じてスチレ
ン−アクリル共重合体エマtレジーンのような樹脂エマ
−レジ1ン、鉛などの金属錯化合物などの触媒、脱落防
止剤、湿潤剤、無機顔料などの各種の添加剤を加えるこ
ともできる。The resin composition for a release material of the present invention may optionally contain a resin such as a styrene-acrylic copolymer Ema-Resine, a catalyst such as a metal complex compound such as lead, a shedding preventive agent, and a wetting agent. , various additives such as inorganic pigments can also be added.
本発明を実施するには前記の酢酸ビニ1し、エチレン、
官能基を儒°するビニIし単量体からなる共嵐合体エマ
tレジ―ンもしくはその変性物にアミノ伺脂およびシリ
コーン−84を重湯で混合して十分Plt件し均一化さ
せればよい。In carrying out the present invention, the above-mentioned vinyl acetate 1, ethylene,
It is sufficient to mix amino resin and silicone-84 with heavy hot water to a co-articulated polymeric resin consisting of vinyl monomers containing functional groups or a modified product thereof, and then thoroughly heat the mixture to homogenize it. .
このようにして僧られる本発明の剥離材料用樹脂組成物
は紙材セロファン、合成樹脂フィルム等の基材に対して
例えばグラビアロールコート注など通帛の塗工方法によ
って塗工して得られ、たとえば工業的、商粟的の各包装
部門におけるラベlし用、シール用裏紙などの加工紙あ
るいは剥離紙と一般に呼称されているものなどに利用さ
れる。The resin composition for a release material of the present invention thus obtained is obtained by coating a base material such as paper cellophane or a synthetic resin film by a conventional coating method such as gravure roll coating. For example, it is used for labels in the industrial and commercial packaging sectors, processed paper such as backing paper for stickers, or what is generally called release paper.
以下実施例を挙げて本発明を説明する。The present invention will be explained below with reference to Examples.
実施例1
酢酸ビニル、エチレン、N−メチロールアクリルアミド
の七ツマー組成比(mlk比)が89=7:4である酢
酸ビニルーエチL/ンーN−メチロ−Iレアクリルアミ
ド共重合体エマルジ値ン(固型分5o、9慮慮%)、メ
ラミン樹Bwとしてスミマー1kM−80W(住友化学
社製品、固型分77.0%)およびシリコーン樹&5M
−7270およびシリコーン樹脂用触媒である5M−7
271をいずれも固型分量で第1表に示した割合で混合
し、これをクラフト紙にバーコータで塗布した。ついで
これを熱風乾燥機で145℃、1分間加熱乾燥して剥離
紙を作成し、室温において剥離試験を行なった。Example 1 Vinyl acetate-ethyl L/N-N-methylolacrylamide copolymer emulsion value (solid form) in which the seven-mer composition ratio (mlk ratio) of vinyl acetate, ethylene, and N-methylolacrylamide is 89 = 7:4. 5 o, 9 consideration%), melamine tree Bw as Sumimar 1km-80W (product of Sumitomo Chemical Co., Ltd., solid content 77.0%) and silicone tree & 5M
-7270 and 5M-7, a catalyst for silicone resins
271 were mixed in the solid amounts shown in Table 1, and the mixture was coated on kraft paper using a bar coater. This was then heated and dried in a hot air dryer at 145° C. for 1 minute to prepare a release paper, and a release test was conducted at room temperature.
すなわち、クラフトテープを上記剥離紙の塗布向に貼り
、2日間放置した後に剥離してその剥離性を評価した。That is, a kraft tape was applied in the coating direction of the release paper, and after being left for 2 days, it was peeled off and its releasability was evaluated.
得られた結果はl乃至10級のスケ−タレ上に記しこれ
を第1表に示した。この場合、1級は極めて容易に剥離
し得て剥離性が非帛に優れていたことを意味し、また1
0級はクラフトテープが剥離紙の塗布面に付着して容易
に剥がれず、剥離性が極めて悪いことを意味する。The results obtained were recorded on scales of grades 1 to 10 and are shown in Table 1. In this case, grade 1 means that it could be peeled off very easily and that the peelability was excellent.
Grade 0 means that the kraft tape adheres to the coated surface of the release paper and is not easily peeled off, meaning that the releasability is extremely poor.
実施例2
実施例1において酢酸ビニダレ−エチレン−N−メチロ
ールアクリCレアミド共重合体工7マルジーンとして酢
酸ビニIし、エチレン、N−メチロールアクリフレアミ
ドの七ツマー組成比(重重比)が76:20:4である
酢酸ビニルーエチレンーN−メチロー−レアクリルアミ
ド共m台体エマ少ジタン(固型分50.8重重ん)を用
いる以外は全く実−例1と同様をこ行なった。得られた
剥離試験の結果をts1表に示す。Example 2 In Example 1, vinyl acetate I was used as vinyl acetate-ethylene-N-methylol acrylamide copolymer 7 Margene, and the seven-mer composition ratio (weight ratio) of ethylene and N-methylol acrylamide was 76: Example 1 was carried out in exactly the same manner as in Example 1, except that a 20:4 vinyl acetate-ethylene-N-methylo-reaacrylamide copolyester (solids content 50.8 weight) was used. The results of the peel test obtained are shown in Table ts1.
比較例1
実施例1および実施例2で用いた#Iビニル框チレンー
N−メチロールアクリIしTi F 共重合体エマIレ
ジ1ン、スミマーtしM−80W、シリコーン樹脂5M
−7270および5M−7271を第1表に示した配−
8副合で混合する以外は実施例1と全く同様に行なった
。剥離試験の結果を第1表に示す。Comparative Example 1 #I vinyl frame used in Example 1 and Example 2 tyrene-N-methylol acrylic I Ti F copolymer Emma I resin 1, Summar t M-80W, silicone resin 5M
-7270 and 5M-7271 as shown in Table 1.
The same procedure as in Example 1 was carried out except that the mixture was mixed in 8 subcombinations. The results of the peel test are shown in Table 1.
手続補正書(自発)
昭和57年lO月 1日
1、事件の表示
昭和57年特許願第 4235号
2、発明の名称
剥#相料用樹脂組成物
3、補正をする者
事件との関係 特許出願人
大阪市東区北浜5丁目15番地
(209) 住友化学工業株式会社
代表者 土 方 武
4、代理人
大阪市東区北浜5丁目15番地
5、補正の対象
明細書の発明の詳細な説明の欄
6、補正の内容
(1)明細書第4頁第17行の、[10重量%以内でプ
ロピオン酸ビニル」とあるを、「10重量%未満で塩化
ビニル、プロピオン酸ビニル」と訂正する。Procedural amendment (voluntary) October 1, 1981, 1, Indication of the case, 1982 Patent Application No. 4235, 2, Name of the invention: Resin composition for exfoliation material 3, Person making the amendment Relationship to the case Patent Applicant 5-15 Kitahama, Higashi-ku, Osaka (209) Sumitomo Chemical Co., Ltd. Representative Takeshi Hijikata 4, Agent 5-15-5 Kitahama, Higashi-ku, Osaka, Detailed description of the invention in the specification to be amended 6. Contents of the amendment (1) On page 4, line 17 of the specification, the phrase [vinyl propionate within 10% by weight] is corrected to read "vinyl chloride, vinyl propionate within 10% by weight."
(2)同第4頁第20行の、「(メタ)アクリル酸エス
テルなど」とあるを、「アクリル酸エステル、メタクリ
ル酸エステルなど」と訂正する。(2) On page 4, line 20, the phrase "(meth)acrylic esters, etc." is corrected to "acrylic esters, methacrylic esters, etc."
以 上that's all
Claims (1)
ル単愈体の組成が重鰍比で70〜9.5=4〜29:1
〜lOである共重合体エマルジーンもしくはその変性物
の20〜90重鳳浩、(Bアミノ#d脂5〜40重量%
および(Qシリコーン樹脂5〜75重量%(いずれも固
型分)を主成分とする剥離材料用樹脂組成物。(2) The composition of vinyl acetate, ethylene, and a vinyl monomer having a functional group is 70 to 9.5 = 4 to 29:1 in deuterium ratio.
20 to 90 copolymer Emulgene or its modified product which is ~1O, (B amino #d fat 5 to 40%
and (Q) A resin composition for a release material containing 5 to 75% by weight (all solid content) of a silicone resin as a main component.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP423582A JPS58120661A (en) | 1982-01-13 | 1982-01-13 | Resin composition for releasing materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP423582A JPS58120661A (en) | 1982-01-13 | 1982-01-13 | Resin composition for releasing materials |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58120661A true JPS58120661A (en) | 1983-07-18 |
JPH0148940B2 JPH0148940B2 (en) | 1989-10-23 |
Family
ID=11578886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP423582A Granted JPS58120661A (en) | 1982-01-13 | 1982-01-13 | Resin composition for releasing materials |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58120661A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1136537A1 (en) * | 2000-03-20 | 2001-09-26 | Akzo Nobel N.V. | Adhesive system |
-
1982
- 1982-01-13 JP JP423582A patent/JPS58120661A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1136537A1 (en) * | 2000-03-20 | 2001-09-26 | Akzo Nobel N.V. | Adhesive system |
WO2001070898A1 (en) * | 2000-03-20 | 2001-09-27 | Akzo Nobel N.V. | Adhesive system comprising etherified amino resins |
Also Published As
Publication number | Publication date |
---|---|
JPH0148940B2 (en) | 1989-10-23 |
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