JPS59145238A - Antistatic treatment solution for vinyl chloride resin - Google Patents

Antistatic treatment solution for vinyl chloride resin

Info

Publication number
JPS59145238A
JPS59145238A JP2006983A JP2006983A JPS59145238A JP S59145238 A JPS59145238 A JP S59145238A JP 2006983 A JP2006983 A JP 2006983A JP 2006983 A JP2006983 A JP 2006983A JP S59145238 A JPS59145238 A JP S59145238A
Authority
JP
Japan
Prior art keywords
graft copolymer
antistatic
graft
vinyl chloride
chloride resin
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
Application number
JP2006983A
Other languages
Japanese (ja)
Other versions
JPS643902B2 (en
Inventor
Kaoru Yamamoto
薫 山本
Keiki Uchiumi
内海 敬喜
Tatsuo Yoshiya
吉屋 達夫
Makoto Nakahira
中平 誠
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.)
Takiron Co Ltd
Original Assignee
Takiron Co Ltd
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 Takiron Co Ltd filed Critical Takiron Co Ltd
Priority to JP2006983A priority Critical patent/JPS59145238A/en
Publication of JPS59145238A publication Critical patent/JPS59145238A/en
Publication of JPS643902B2 publication Critical patent/JPS643902B2/ja
Granted legal-status Critical Current

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  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:The titled treatment solution capable of imparting antistatic property inexpensively to a PVC substrate, obtained by graft-polymerizing a vinyl monomer or a vinylidene monomer with a rubbery trunk polymer of a low volume specific resistivity and dissolving the graft copolymer in a solvent. CONSTITUTION:A rubbery trunk polymer of a low volume specific resistivity is produced by copolymerizing 10-50wt% monomer containing about 4-500 alkylene oxide groups with 90-50wt% conjugated diene or acrylic ester. A vinyl monomer or a vinylidene monomer is graft-polymerized with the produced rubbery trunk polymer. 5-40pts.wt. produced graft copolymer is dissolved in 100pts.wt. solvent selected from the group consisting of ethyl acetate, methyl ethyl ketone, and tetrahydrofuran to obtain the antistatic treatment solution. When this solution is applied to a PVC substrate and dried, the surface electric resistivity of the substrate becomes about 10<10>-10<12> and is accorded with antistatic property.

Description

【発明の詳細な説明】 本発明は各種弱電機器、その製造装Ujtや取扱い開運
用具、クリーンルーム用材、家庭用電気器具、音響徐器
等のケーシング材或いは包装用品更には建材等に供せら
れる塩化ビニル樹脂プレート若しくはシート等に塗布し
、該プレート若しくはシートの表面抵抗率を下げてこれ
に制電性を付与する為の新島な制電性処理液に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to various types of light electrical appliances, their manufacturing equipment, handling and operation tools, clean room materials, household electrical appliances, casing materials such as acoustic decomposers, packaging materials, and even building materials. This invention relates to a unique antistatic treatment liquid that is applied to a vinyl resin plate or sheet to lower the surface resistivity of the plate or sheet and impart antistatic properties to it.

本出願人は実願昭57−107154に於て、ポリ塩化
ビニル樹脂基材の少なくとも片面に、体積固有抵抗率の
小なるゴム幹重合体にビニル単量体又はビニリデン単量
体をグラフト重合することによって得られたグラフト共
重合体の制電性被段層を熱圧一体として成る訓電性合成
樹脂積層物を提供した。これは上記グラフト共重合体が
優れた制電特性を有するにもかかわらず、曲げ弾性率、
引張強度、伸び率等の物理的性能に劣る為に成形加工性
に乏しく、また可燃性で高価であることから、前記の如
き用途には未だ実用化されていなかった実情にらみ、上
記グラフト共重合体と塩化ビニル樹脂とを熱圧一体とす
ることによって、前者゛の乏しい物理的性能を後者をし
て補完せしめ且つその優れた制m、特性をそのまま活か
し、上記用途に好適に採用されるよう図ったものである
In Utility Model Application No. 57-107154, the present applicant graft-polymerized a vinyl monomer or a vinylidene monomer onto at least one side of a polyvinyl chloride resin base material to a rubber base polymer having a small specific volume resistivity. An antistatic synthetic resin laminate is provided in which the antistatic layer of the graft copolymer obtained by this method is integrated with heat and pressure. This is because although the above graft copolymer has excellent antistatic properties, the flexural modulus
In view of the fact that the above-mentioned graft copolymer has not yet been put to practical use in the above applications because it has poor moldability due to poor physical properties such as tensile strength and elongation rate, and is flammable and expensive, By combining the coalescence and vinyl chloride resin into one body under heat and pressure, the poor physical performance of the former is complemented by the latter, and its excellent control and properties are utilized as they are, making it suitable for use in the above-mentioned applications. It was planned.

斯る制電性合成樹脂積層物は、その際立った帯電防止効
果と良好な物理的性能とが重奏されるから、上記ケーシ
ング材或いは包装用品更には建材等の工業材料として極
めて好適であるが、該積層物は塩化ビニル樹脂基材と上
記グラフト共重合体とを熱圧一体として成る為、両面に
グラフト共重合体を積11−Iしても端部は上記基材が
露出し、亦、これらを溶接によって互いに接合して各種
形状の物品を構成する場合、或いは切削加工を施す場合
等に於ては溶接部或いは切削凹所に塩化ビニル樹脂が露
出することは避けられず、従ってこの露出部分が制電性
を稍々減退させる原因となることも否めなかった。
Such antistatic synthetic resin laminates have outstanding antistatic effects and good physical performance, so they are extremely suitable as industrial materials such as the above-mentioned casing materials, packaging products, and even building materials. Since the laminate is made of a vinyl chloride resin base material and the above-mentioned graft copolymer integrated into one body under heat and pressure, even if the graft copolymer is laminated on both sides (11-I), the above-mentioned base material is exposed at the edges, and When these are joined to each other by welding to construct articles of various shapes, or when cutting is performed, it is inevitable that vinyl chloride resin will be exposed in the welded parts or cutting recesses, and therefore, this exposure It was also undeniable that this part caused a slight decrease in antistatic properties.

本発明者等は上記先行技術をもとに更に研究を重ねた結
果、前記グラフト共重合体を薄膜として塩化ビニル樹脂
基材に塗着すれば、上記同様の制電性効果が得られるこ
とを知見すると共に上記問題点を一帰することが出来且
つ更にコストの低減を図ることに成功するに至ったので
あり、本発明は斯る技術的背景によってなされた新規な
塩化ビニル樹脂用制電性処理液を提供するものである。
As a result of further research based on the above-mentioned prior art, the present inventors have found that the same antistatic effect as above can be obtained by applying the above-mentioned graft copolymer as a thin film to a vinyl chloride resin base material. With this knowledge, we were able to eliminate the above problems and further reduce the cost.The present invention is a novel antistatic property for vinyl chloride resin that was made based on this technical background. It provides a processing liquid.

即ち、本発明は体積固有抵抗率の小なるゴム幹i−[合
体にビニル単量体又はビニリデン単量体をグラフト重合
することによって得られたグラフト共、爪合体5〜40
6部を酢酸エチル、メチルエチルケトン及びテトラヒド
ロフランより選ばれた一種の溶剤100重量部に溶解し
て成ることを特徴とする塩化ビニル樹脂用制電性処理液
である。グラフト共重合体は、上記の如く体積固有抵抗
率が小さいゴム幹重合体にビニル単量体又はビニリデン
単量体をグラフト重合することによって得られるもので
永久的な帯電防止効果(制電性)を有する透明物質であ
る。このゴム幹重合体は4〜500個のアルキレンオキ
サイド基を有する単量体10〜50重量%と共役ジエン
及びアクリルエステルから選ばれた一種以上の単量体9
0〜50重景%か重紙る共重合体であり、上記グラフト
共重合体が帯電防止効果を有する所以は、このゴム幹本
合体の相が加工時に枝重合体相中に互いにブリッジ状態
をなして分散しており、電荷が主としてこのゴム幹重合
体相中を通って拡散、減衰するからであるとされている
。しかもアルキレンオキサイド基はゴム幹重合体に化学
的に結合しているので過酷な水洗によっても制電性が低
下することがなく、従って永久的な帯電防止効果も保証
するものである。
That is, the present invention provides rubber bases with low specific volume resistivity, i-[glyphs obtained by graft polymerization of vinyl monomers or vinylidene monomers on the aggregates, and nail aggregates 5 to 40
6 parts by weight of a solvent selected from ethyl acetate, methyl ethyl ketone and tetrahydrofuran. Graft copolymers are obtained by graft polymerizing vinyl monomers or vinylidene monomers onto a rubber base polymer with a low specific volume resistivity as described above, and have a permanent antistatic effect (antistatic property). It is a transparent substance with This rubber backbone polymer contains 10 to 50% by weight of a monomer having 4 to 500 alkylene oxide groups and 9 to 9% of one or more monomers selected from conjugated dienes and acrylic esters.
The graft copolymer has an antistatic effect due to the fact that the phase of this rubber trunk body forms a bridge state with each other in the branch polymer phase during processing. This is said to be because the charge mainly diffuses and attenuates through the rubber base polymer phase. Moreover, since the alkylene oxide group is chemically bonded to the rubber backbone polymer, the antistatic properties will not deteriorate even after severe washing with water, thus ensuring a permanent antistatic effect.

上記グラフト共重合体は酢酸エチル、メチルエチルケト
ン或いはテトラヒドロフラン等の溶剤に可溶であり、該
溶剤のいずれか一種1oo重量部に上記グラフト共重合
体5〜40重紙部を溶解せしめた液状物を塩化ビニル樹
脂基板の表面に塗布して溶剤を揮散させると該グラフト
共重合体の硬化薄11かが形成され、この薄膜の形成に
よって塩化ビニル樹脂基板の表面電気抵抗率が約101
0〜1012Ωとなl)#!A’f’O−制電性が付与
されるのである。
The above-mentioned graft copolymer is soluble in a solvent such as ethyl acetate, methyl ethyl ketone, or tetrahydrofuran, and a liquid obtained by dissolving 5 to 40 parts by weight of the above-mentioned graft copolymer in 10 parts by weight of any one of the solvents is chlorinated. When the graft copolymer is applied to the surface of the vinyl resin substrate and the solvent is evaporated, a cured thin film of the graft copolymer is formed, and the surface electrical resistivity of the vinyl chloride resin substrate is increased to about 101 by the formation of this thin film.
0 to 1012 Ω) #! A'f'O- antistatic properties are imparted.

この応用例を添付図面に基づき説明すると、第1図は厚
み1〜10順の塩化ビニル樹脂基板1の両面に上記液状
物をロールコータ、フローコータ或いは刷毛塗り等によ
って塗布して特に限定はされないが厚み約20〜200
μ(ミクロン)の上記グラフト共重合体の薄膜2.2を
形成したものを示す。亦、第2図は両面にグラフト共重
合体の被覆層8.8を熱圧一体とした塩化ビニル樹脂基
板1(前記実願昭57−107154で開示した積層物
)の端面に上記同様に薄膜2.2を形成せしめたもの、
更に第8図は第2図で採用した基板1′・1同志の溶接
接合部に同じく薄膜2を形成せしめたもの、第4図は切
削加工が施されて塩化ビニル樹脂が露出された上記基板
1の切削凹所に同様に薄膜2・・・を形成せしめたもの
を夫々示す。第1図の応用例は上記先行技術に於ける積
層°物の被覆層を薄膜2.2に代替したのと同様である
が、表面電気抵抗率は制電性を呈するに充分低くまた薄
膜2.2の基板lに対する密着性も極めて強固であり、
従って上記積層物と同様の用途に供することが出来る上
に、制電性物質の実体であるグラフト共重合体が薄膜2
.2とされるから、該グラフト共重合体の実質的な使用
示は少なくて済みそれだけコストメリットが付加される
。尚、図例の基板1の端面にもグラフト共重合体の薄膜
を形成し得ることは当然であり、このように基板1の外
周を全て薄膜で覆う場合上記塗装法の他にディッピング
法によっても可能であることは云うまでもない。第2図
乃至第4図の応用例は上記先行技術に係る積層物1′の
塩化ビニル樹脂の露出部に本発明の処理液を塗布してグ
ラフト共重合体の薄膜2・・・を形成せしめ、これによ
って積層物1′の制電特性を補完するものであり、従っ
て本発明の処理液は局所的な制m性の付与に極めて好適
であることが容易に理解されよう。亦、図には示さない
が既に形成された塩化ビニル樹脂より成る形状物を爾後
的に制電処理する場合でも、本発明の処理液を塗布する
だけでその目的は達成されると共に複雑な形状でも隈無
くそれが可能である。
This application example will be explained based on the attached drawings. In Fig. 1, the above liquid material is applied to both sides of a vinyl chloride resin substrate 1 having a thickness of 1 to 10 using a roll coater, a flow coater, a brush coating, etc., and there is no particular limitation. The thickness is about 20~200mm
A thin film 2.2 of the above-mentioned graft copolymer having a diameter of μ (microns) is shown. In addition, FIG. 2 shows a thin film similar to that described above on the end face of a vinyl chloride resin substrate 1 (laminate disclosed in the above-mentioned Utility Model Application No. 107154/1983), which has a coating layer 8.8 of a graft copolymer integrated on both sides by heat and pressure. 2. What led to the formation of 2.
Furthermore, FIG. 8 shows the same thin film 2 formed on the welded joint between the substrates 1' and 1 used in FIG. A thin film 2... is similarly formed in the cut recess of No. 1, respectively. The application example shown in FIG. 1 is similar to the prior art in which the coating layer of the laminate is replaced with the thin film 2.2, but the surface electrical resistivity is sufficiently low to exhibit antistatic properties, and the thin film 2. The adhesion to the substrate l of .2 is also extremely strong,
Therefore, the thin film 2 can be used for the same purpose as the above-mentioned laminate, and the graft copolymer, which is the substance of the antistatic substance,
.. 2, the actual usage of the graft copolymer is required to be reduced, which adds cost advantages. It goes without saying that a thin film of the graft copolymer can also be formed on the end surface of the substrate 1 in the example shown in the figure, and when the entire outer periphery of the substrate 1 is covered with a thin film in this way, in addition to the above-mentioned coating method, a dipping method can also be used. Needless to say, it is possible. In the application example shown in FIGS. 2 to 4, the treatment liquid of the present invention is applied to the exposed portion of the vinyl chloride resin of the laminate 1' according to the prior art to form a thin film 2 of the graft copolymer. It is easy to understand that this complements the antistatic properties of the laminate 1', and therefore the treatment liquid of the present invention is extremely suitable for imparting local antistatic properties. Although not shown in the drawings, even if an object made of vinyl chloride resin that has already been formed is to be subjected to antistatic treatment, the purpose can be achieved by simply applying the treatment liquid of the present invention, and even complex shapes can be treated. But it is absolutely possible.

更に、従来よりプラスデック材料の?Id電防電防衣用
表面処理剤て導電性塗料或いは界面活性剤が採用されて
おり、これらは、前者は一般にカーボン等により着色さ
れているので透光性を必要とする用途には不可であり、
一方後者は雰囲気湿度の彫物が大であり且つ水洗後は制
電性が消失する・・・等の問題点を内包していたが、本
発明の処理液によって形成される上記グラフト共重合体
の薄膜は透明物質であるから基板1の色相をそのまま活
がずことが出来、また前述の如く過酷な水洗によっても
制電性が低下することがないから、基板1と、の層間剥
離を起こさない限り永久的な?Vm防止効果を有するも
のであり、これらの点でも本発明の処理液は従来の帯電
防止用表面処理剤をはるかに凌ぐものであると云える。
Furthermore, is the material of Plus Deck better than before? Conductive paints or surfactants are used as surface treatment agents for Id electrical protection coatings, and the former are generally colored with carbon, etc., so they cannot be used in applications that require translucency. can be,
On the other hand, the latter has problems such as a large degree of atmospheric humidity and loss of antistatic properties after washing with water. Since the thin film is a transparent material, the hue of the substrate 1 can be preserved as it is, and as mentioned above, the antistatic properties will not deteriorate even after severe washing with water, so delamination between the thin film and the substrate 1 will not occur. As long as permanent? It has a Vm preventing effect, and it can be said that the treatment liquid of the present invention far exceeds conventional antistatic surface treatment agents in these respects as well.

次に表1に本発明の実施例を比較例と共に掲げ比較対照
する。
Next, Table 1 lists Examples of the present invention together with Comparative Examples for comparison and contrast.

(以下余 白) (表 1) (注)×1.各種溶剤に本発明に係るグラフト共重合体
を溶解させその溶解性を目視判定した。
(Margin below) (Table 1) (Note) ×1. The graft copolymer according to the present invention was dissolved in various solvents, and its solubility was visually determined.

X 2.  厚さ5間の塩化ビニル樹脂板の両面にグラ
フト共重合体を溶解した溶剤を塗布し、表面に約20〜
200μのグラフト共重合体の薄膜を形成したものにつ
いて表面電気抵抗率を測定した。
X 2. A solvent in which the graft copolymer was dissolved was applied to both sides of a vinyl chloride resin plate with a thickness of 5 to 100 ml.
The surface electrical resistivity was measured for a thin film of the graft copolymer having a thickness of 200 μm.

×3.密着性はゴバン目試験法により行ない、O・・・
良好、 △・・・稍々良、 ×・・・良くない、ことを
夫々示す。
×3. Adhesion was determined by the cross-cut test method, and O...
Good, △: Fairly good, ×: Not good.

表1(7)総合的評価により酢酸エチル、テトラヒドロ
フラン及びメチルエチルケトンが上記グラフト共重合体
の溶剤として最も適当であることが判明した。また、斯
る溶剤100mfit部に対し、グラフト共重合体の溶
解示が5重量部未満の場合は制tg性塗膜の膜厚が充分
に確保されにくい傾向となり、一方40重患部を超える
と処理液の粘性が高くなって作業性に難を来たすことと
必要以上の膜厚を得る傾向となる。
Table 1 (7) Comprehensive evaluation revealed that ethyl acetate, tetrahydrofuran and methyl ethyl ketone were the most suitable solvents for the graft copolymer. Furthermore, if the amount of graft copolymer dissolved in 100 mfit parts of the solvent is less than 5 parts by weight, it will be difficult to ensure a sufficient thickness of the anti-tg coating film, whereas if it exceeds 40 parts by weight, treatment will be difficult. The viscosity of the liquid becomes high, which makes workability difficult and tends to result in a film that is thicker than necessary.

叙述の如く本発明の処理液は塩化ビニル樹脂材料及びそ
の成形物の極めて有用性の高い帯電防止剤であって、利
用価値は頗る大である。
As described above, the treatment liquid of the present invention is an extremely useful antistatic agent for vinyl chloride resin materials and molded products thereof, and has extremely high utility value.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図乃至第4図は本発明の応用例を示す縦断面図であ
る。 (符号の説明) l・・・塩化ビニル樹88基板、1・・稍n物、2・・
・グラフト共重合体の薄膜、3・・・グラフト共重合体
の被覆層。 一以 上−
1 to 4 are longitudinal sectional views showing an example of application of the present invention. (Explanation of symbols) 1... Vinyl chloride tree 88 substrate, 1... Small material, 2...
- Thin film of graft copolymer, 3... Covering layer of graft copolymer. One or more -

Claims (1)

【特許請求の範囲】[Claims] 1、体積固有抵抗率の小なるゴム幹重合体にビニル単爪
体又はビニリデン単量体をグラフト重合することによっ
て得られたグラフト共重合体5〜40重F1部を酢酸エ
チノペメチルエチルケトン及びテトラヒドロフランより
選ばれた一種の溶剤100重片(部に溶解して成ること
を特徴とする塩化ビニル樹脂用制電性処理液。
1. 1 part of a 5 to 40 weight F graft copolymer obtained by graft polymerizing a vinyl monoclaw or a vinylidene monomer to a rubber base polymer with a small specific volume resistivity is mixed with etynopex acetate methyl ethyl ketone and tetrahydrofuran. An antistatic treatment liquid for vinyl chloride resin, characterized in that it is formed by dissolving 100 parts of a selected kind of solvent.
JP2006983A 1983-02-08 1983-02-08 Antistatic treatment solution for vinyl chloride resin Granted JPS59145238A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006983A JPS59145238A (en) 1983-02-08 1983-02-08 Antistatic treatment solution for vinyl chloride resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006983A JPS59145238A (en) 1983-02-08 1983-02-08 Antistatic treatment solution for vinyl chloride resin

Publications (2)

Publication Number Publication Date
JPS59145238A true JPS59145238A (en) 1984-08-20
JPS643902B2 JPS643902B2 (en) 1989-01-24

Family

ID=12016804

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006983A Granted JPS59145238A (en) 1983-02-08 1983-02-08 Antistatic treatment solution for vinyl chloride resin

Country Status (1)

Country Link
JP (1) JPS59145238A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04111601U (en) * 1991-03-13 1992-09-29 横河電機株式会社 Programming panel mounting mechanism

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5536237A (en) * 1978-09-06 1980-03-13 Kureha Chem Ind Co Ltd Antistatic resin composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5536237A (en) * 1978-09-06 1980-03-13 Kureha Chem Ind Co Ltd Antistatic resin composition

Also Published As

Publication number Publication date
JPS643902B2 (en) 1989-01-24

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