JPS6330940B2 - - Google Patents

Info

Publication number
JPS6330940B2
JPS6330940B2 JP56138537A JP13853781A JPS6330940B2 JP S6330940 B2 JPS6330940 B2 JP S6330940B2 JP 56138537 A JP56138537 A JP 56138537A JP 13853781 A JP13853781 A JP 13853781A JP S6330940 B2 JPS6330940 B2 JP S6330940B2
Authority
JP
Japan
Prior art keywords
vinyl chloride
pasting
static electricity
film
charges
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
Application number
JP56138537A
Other languages
Japanese (ja)
Other versions
JPS5840339A (en
Inventor
Tokio Mera
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP13853781A priority Critical patent/JPS5840339A/en
Priority to GB08225185A priority patent/GB2108047B/en
Priority to DE19823232834 priority patent/DE3232834A1/en
Publication of JPS5840339A publication Critical patent/JPS5840339A/en
Publication of JPS6330940B2 publication Critical patent/JPS6330940B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Description

【発明の詳細な説明】 本発明は、接着剤を使用することなく貼付け場
所の変更・繰り返しの貼付け使用を可能ならし
め、剥離後に生じる貼付け面の貼付け痕跡が生ぜ
ず、貼付け作業による汚損のない貼付けが可能な
持続性静電気付着力を付与した塩化ビニルフイル
ムに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention enables changing the pasting location and repeated pasting without using adhesives, and eliminates the appearance of pasting traces on the pasting surface after peeling off, and eliminates stains caused by pasting work. This invention relates to a vinyl chloride film that has a durable electrostatic adhesive force that can be pasted.

従来の接着(貼着)手段は、接着剤を使用する
ことが大部分である。しかし、接着剤を使用して
貼着することは、一旦貼着した後は剥離すること
が困難であることから一回のみの使用しかでき
ず、貼付け場所の変更や繰り返しの貼付け使用は
できない。また、剥離後は、貼付け面の貼付け痕
跡が生ずるため、使用後の清掃処理の手数がかか
つたり、使用場所に限定を受ける等の欠点があ
る。
Conventional adhesion (adhesion) means mostly involve the use of adhesives. However, when pasting using an adhesive, it is difficult to peel off once it has been pasted, so it can only be used once, and the pasting location cannot be changed or the pasting cannot be repeated. Further, after peeling off, traces of pasting are left on the pasting surface, so there are disadvantages such as the troublesome cleaning process after use and restrictions on the place of use.

本発明は、このような点に鑑み静電気付着力を
利用して貼着できる塩化ビニルフイルムを提供
し、もつて前記欠点を解決せんとするものであ
る。
In view of these points, the present invention provides a vinyl chloride film that can be attached using electrostatic adhesive force, thereby solving the above-mentioned drawbacks.

塩化ビニルフイルム・シート類が摩擦帯電し静
電気を発生することはよく知られている。従来、
このことは静電気障害として認識され、専ら静電
気の発生防止に問題が集中し、帯電防止油剤をは
じめ各種の帯電防止策が提案されている。
It is well known that vinyl chloride films and sheets are triboelectrically charged and generate static electricity. Conventionally,
This problem is recognized as a static electricity problem, and the problem is mainly focused on preventing the generation of static electricity, and various antistatic measures including antistatic oil agents have been proposed.

ところが、本発明は、静電気による付着力をフ
イルム類の貼付けに積極的に利用しようとするも
ので、従来にない全く新らしい試みである。
However, the present invention actively utilizes the adhesive force caused by static electricity for pasting films, and is a completely new attempt never seen before.

ここで、塩化ビニルフイルム・シート類が摩擦
帯電し静電気を発生するとしても、静電気は時間
とともに減少し付着力がなくなるから、そのまま
では商品として使用できない。商品として使用で
きるためには、静電気が多量に発生し静電気付着
力が強く、発生した静電気が時間とともに減少せ
ず長時間持続することが必要であるから、従来に
ない新らしい技術の研究が必要である。
Here, even if vinyl chloride films and sheets are triboelectrically charged and generate static electricity, the static electricity decreases over time and the adhesive force disappears, so they cannot be used as products as they are. In order to be used as a product, a large amount of static electricity must be generated, the static adhesive force must be strong, and the generated static electricity must not decrease over time and last for a long time, so research on new and unprecedented technology is required. It is.

従来の摩擦静電気よりも一層多量の電荷をフイ
ルム・シート類が保有し得るためには、電荷はフ
イルム・シート類の表面だけに存在することな
く、その内部にまで拡散することが望ましい。ま
た、静電気が時間とともに減少しないためには、
フイルム・シート材によつて電荷が捕獲状態(ト
ラツプ)になることが望ましい。即ち、電気量が
体積内へ侵入拡散しやすく、かつ拡散位置でトラ
ツプされるならば、従来のものに比し電荷が表面
のみでなく体積内にも存在するということから単
位重量当りの電気量は大きくなるし、体積内へ侵
入拡散するがゆえに表面からみたときの分布状態
は、従来の表面のみの帯電にくらべ一様に近い状
態に近づく。また、体積内でトラツプされた電荷
は、一種のエレクトレツト状態であるから時間と
ともに減少する恐れもない。
In order for films and sheets to be able to retain a larger amount of charge than conventional tribostatic electricity, it is desirable that the charges not only exist on the surface of the film and sheets but also diffuse into the interior thereof. Also, in order to prevent static electricity from decreasing over time,
It is desirable that the charge be trapped by the film/sheet material. In other words, if the quantity of electricity easily penetrates and diffuses into the volume and is trapped at the diffusion position, the quantity of electricity per unit weight is becomes large, and because it penetrates and diffuses into the volume, the distribution state when viewed from the surface is closer to a uniform state than in the conventional case where only the surface is charged. Furthermore, since the charges trapped within the volume are in a kind of electret state, there is no fear that they will decrease over time.

従つて、電荷の内部への侵入拡散を促進する促
進材及び内部へ侵入拡散した電荷が再び外部へ浸
出することによつて電荷が減少することを防止す
る電荷捕獲材を、塩化ビニル樹脂に混合すれば、
従来のものよりはるかに優れた持続性静電気付着
力を有するフイルム・シート類が製造できる。し
かし、電荷の内部への侵入拡散を促進する材料
は、当然内部から外部へ浸出拡散することも促進
するから、長期の静電気付着力を付与することに
はならない。この点から、前記材料は、一方向性
すなわち整流作用に類似した侵入拡散を促進する
が、浸出拡散能の小さい材料で、かつ電荷トラツ
プ能に優れたものでなければならない。電気回路
的な等価表現をすれば、内部にトラツプされた電
荷が貼着面を隔ててコンデンサーを形成し、コン
デンサーとしての絶縁抵抗は、整流作用的な抵抗
特性を有するものでなければならない。
Therefore, a promoting material that promotes the infiltration and diffusion of charges into the interior and a charge trapping material that prevents charges from being reduced due to the charges that have penetrated and diffused inside leaking out again are mixed into the vinyl chloride resin. if,
It is possible to produce films and sheets that have a much better sustained electrostatic adhesion than conventional ones. However, a material that promotes the infiltration and diffusion of charges into the interior naturally also promotes the leaching and diffusion of charges from the inside to the outside, and therefore does not provide long-term electrostatic adhesion. From this point of view, the material must be unidirectional, that is, a material that promotes intrusion diffusion similar to a rectification effect, but has a low percolation and diffusion ability, and has an excellent charge trapping ability. Expressed equivalently in terms of an electric circuit, the charges trapped inside form a capacitor across the adhesive surface, and the insulation resistance of the capacitor must have rectifying resistance characteristics.

本発明者は、このような観点から鋭意研究の結
果発明したもので、その要旨は、炭素数40〜60の
有機ケトンを塩化ビニルに対して1〜3重量%の
範囲で配合することを特徴とするものである。
The inventor of the present invention has made this invention as a result of intensive research from this point of view, and its gist is that an organic ketone having a carbon number of 40 to 60 is blended in a range of 1 to 3% by weight based on vinyl chloride. That is.

塩化ビニルフイルム・シート類であることから
その製造において、帯電防止効果のある材料の使
用を全く排除して製造しても、例えば、可塑剤に
おいても帯電防止能力のあるもの、無いもの或い
は電荷発生能力のあるもの等があるが、帯電防止
能力のあるものは排除し、積極的に電荷発生能力
のあるものを使用して、例えば、電荷の発生しや
すい可塑剤として、パラフイン系金属塩などの
金属分子含有分子、ポリビニルクロライドの金
属錯体、ポリSchiff塩基などの金属架橋有機中分
子、スクアリン酸金属錯体、キレート型中分子
量錯体、金属シアノ錯体中分子などの配位結合を
有する中分子、ビニルピリジユームエステル、
ポリビニルピリジユーム塩類、フタロシアニン塩
類などの混合型中分子化合物、ピロメツトニト
リル誘導体、ピロメリツト酸誘導体、ポリテトラ
シアノエチレン類などの寄木細工状中分子、等を
配合して製造しても、電荷は多量に発生し静電気
付着力は強くなるから、静電気付着力の点からは
これでも充分であるが、本発明が炭素数40〜60の
有機ケトンを配合するのは、更に電荷の捕獲能を
顕著にし、電荷の侵入拡散を促進し、フイルム
面、特にフイルムの摩擦面に一方向性電荷移転層
を形成し静電気が長時間持続し、塩化ビニル樹脂
の相溶性高く電荷を体積内へ均等拡散し樹脂内に
おける分散能を良好にするためである。
Because they are vinyl chloride films and sheets, even if they are manufactured without using any materials that have an antistatic effect, for example, plasticizers may or may not have antistatic ability, or they may generate charges. However, those with antistatic ability should be excluded and those with charge generation ability should be actively used. Molecules containing metal molecules, metal complexes of polyvinyl chloride, metal-crosslinked organic medium molecules such as polySchiff bases, medium molecules with coordination bonds such as squaric acid metal complexes, chelate-type medium molecular weight complexes, metal cyano complex medium molecules, vinylpyri Dium ester,
Even when manufactured by blending mixed medium-molecular compounds such as polyvinylpyridium salts and phthalocyanine salts, parquet-like medium-molecular compounds such as pyromethonitrile derivatives, pyromellitic acid derivatives, and polytetracyanoethylenes, the charge remains unchanged. This is sufficient from the standpoint of electrostatic adhesion, as it is generated in large quantities and the electrostatic adhesion becomes strong, but the reason why the present invention incorporates an organic ketone with a carbon number of 40 to 60 further increases the charge trapping ability. It promotes charge penetration and diffusion, forms a unidirectional charge transfer layer on the film surface, especially on the friction surface of the film, maintains static electricity for a long time, and has high compatibility with vinyl chloride resin, which allows charge to spread evenly within the volume. This is to improve the dispersibility within the resin.

ここで、有機ケトンを炭素数40〜60の中分子量
のものに限定したのは、炭素数が40より少ないも
のでは、有機ケトンが析出し、分離してしまうか
らであり、又60より多い場合は分子量が大きくな
りすぎるために混合した場合に均一な混合が困難
となるからである。又、有機ケトンの配合割合は
1重量%未満であると電荷捕獲能が不充分とな
り、3重量%を超えると塩化ビニルフイルムの機
械的性質が弱くなり伸びたり皺が発生し易くなる
ため好ましくない。
Here, we limited the organic ketones to those with a medium molecular weight of 40 to 60 carbon atoms because if the number of carbon atoms is less than 40, the organic ketone will precipitate and separate. This is because the molecular weight becomes too large, making it difficult to mix uniformly when mixed. Furthermore, if the blending ratio of organic ketone is less than 1% by weight, the charge trapping ability will be insufficient, and if it exceeds 3% by weight, the mechanical properties of the vinyl chloride film will become weak and it will be easy to stretch and wrinkle, which is not preferable. .

塩化ビニルフイルムの厚さは、あまり薄いと皺
がより易く又剥がし難たく、あまり厚いと貼着面
になじみ難たいので、20〜450μ位の範囲がよい。
The thickness of the vinyl chloride film is preferably in the range of about 20 to 450 μm, because if it is too thin, it will wrinkle more easily and be difficult to peel off, and if it is too thick, it will be difficult to adapt to the surface to which it is attached.

有機ケトンは、ステアリン酸金属塩類、例えば
ステアリン酸マグネシユーム、ステアリン酸カル
シユーム塩から誘導した変成ケトンが好適であ
る。ステアリン酸マグネシユームから誘導した変
成ケトンは次のような反応過程を経て製造され
る。
The organic ketone is preferably a modified ketone derived from a metal stearate, such as magnesium stearate or calcium stearate. A modified ketone derived from magnesium stearate is produced through the following reaction process.

ステアリン酸(溶融温度略55℃)100Kgを150℃
近傍に加温した溶融槽にて溶融し、その溶融ステ
アリン酸を撹拌しながら、これに5Kgの苛性マグ
ネシア粉を1回当たり50〜100gずつにして上方
より順次投入する。投入初期に、苛生マグネシア
とステアリン酸との反応によるステアリン酸マグ
ネシユームが生成され、かつ溶融点の上昇をきた
す。このため、溶融槽は150℃近傍に保持するよ
う加温をつづける。反応時間約15分で変成ステア
リンが熟成される。
Stearic acid (melting temperature approx. 55℃) 100Kg at 150℃
The molten stearic acid is melted in a heated melting tank nearby, and 5 kg of caustic magnesia powder is sequentially added from above at a rate of 50 to 100 g at a time while stirring the stearic acid. At the beginning of charging, magnesium stearate is produced by the reaction between caustic magnesia and stearic acid, and the melting point increases. For this reason, the melting tank continues to be heated to maintain it at around 150°C. Modified stearin is matured in a reaction time of approximately 15 minutes.

苛生マグネシア投入の目的の一つは、ステアリ
ン酸マグネシユーム塩の反応原料として使用する
ことであり、他の目的はステアリン酸マグネシユ
ーム塩を変成ケトン化する触媒として使用するこ
とであるから、ステアリン酸及びステアリン酸マ
グネシユーム塩が熱分解を生じないが、反応が速
やかに進行するよう150℃近傍に保持する必要が
あるものである。
One purpose of adding caustic magnesia is to use it as a reaction raw material for magnesium stearate, and another purpose is to use it as a catalyst for converting magnesium stearate into modified ketonization. Although magnesium stearate does not undergo thermal decomposition, it is necessary to maintain the temperature around 150°C so that the reaction proceeds quickly.

変成ステアリンが熟成されたところで、それを
撹拌しながら、発煙濃塩酸10Kgを槽内に連続的に
流入し、約10〜15分間接触反応させることによつ
て、炭素数40〜60の有機ケトンを得た。この有機
ケトンは多量の副次生成物と塩化マグネシユーム
が含有されているので、数回にわたる沸騰水によ
る洗浄を通じ水に可溶の成分を除去することが必
要である。また、副次的に生成する小分子量の水
に不溶の成分を、低沸点成分とともに、真空蒸留
槽で分別蒸留することにより除去する。以上によ
り、60Kgの目的物を収量として得た。
Once the modified stearin has been aged, 10 kg of fuming concentrated hydrochloric acid is continuously flowed into the tank while stirring, and a contact reaction is carried out for about 10 to 15 minutes to produce organic ketones with carbon numbers of 40 to 60. Obtained. Since this organic ketone contains a large amount of by-products and magnesium chloride, it is necessary to remove water-soluble components through several washings with boiling water. In addition, water-insoluble components of small molecular weight that are produced as a by-product are removed together with low-boiling components by fractional distillation in a vacuum distillation tank. As a result of the above, 60 kg of the target product was obtained.

次に、このようにして得られた変成ケトンを、
塩化ビニルに対して2重量%配合し、均一に混合
してフイルム状に成型し本発明に係る静電気付着
力を付与した塩化ビニルフイルムとした。
Next, the modified ketone obtained in this way is
It was blended in an amount of 2% by weight based on vinyl chloride, mixed uniformly, and formed into a film to obtain the vinyl chloride film imparted with electrostatic adhesion according to the present invention.

しかして、本発明に係る塩化ビニルフイルム
は、強い静電気付着力が長時間持続するため、適
宜の平面、例えばウインド面、壁面、ロツカー、
家具、机、書棚等に静電気付着させて貼付けるこ
とができるし、貼付け場所の変更・繰り返しの貼
付け使用ができる。しかも、本発明に係る塩化ビ
ニルフイルムは、剥離後に貼付け痕跡も生じな
い。
Therefore, the vinyl chloride film according to the present invention has a strong electrostatic adhesive force that lasts for a long time, so it can be used on any suitable flat surface, such as a window surface, a wall surface, a rocker, etc.
It can be attached to furniture, desks, bookshelves, etc. with static electricity, and the attachment location can be changed and the attachment can be used repeatedly. Moreover, the vinyl chloride film according to the present invention does not leave any traces of pasting after being peeled off.

従つて、本発明は、貼付けて使用するもの、貼
付けたり剥離したりして使用するもの、例えば、
広告・案内等の用紙、黒板・掲示板・伝言板に替
わる用紙、メモ用紙、各種遊びのシール…等には
最適である。この際、使用するものに合せそれぞ
れ加工を施すことはもちろんである。例えば、フ
イルム面に印刷したり、貼着したり、あるいは製
造に際し顔料を配合し着色したりする如くであ
る。
Therefore, the present invention is applicable to products that are used by pasting, products that are used by pasting and peeling, for example,
It is ideal for use as paper for advertisements and guidance, as a substitute for blackboards, bulletin boards, and message boards, as memo paper, as stickers for various types of games, etc. At this time, it is of course necessary to process each material according to the material to be used. For example, the surface of the film may be printed or pasted, or pigments may be mixed and colored during production.

尚、本発明に係る塩化ビニルフイルムの帯電特
性の試験結果は、次の通りであつた。
The test results of the charging characteristics of the vinyl chloride film according to the present invention were as follows.

厚さ50μのフイルム900mm×600mmと200mm×400
mmの大きさで、表面に五色印刷済みのものを、温
度5〜28℃、湿度20〜73%の環境下で、垂直にお
いた金属板に摩擦して昭和56年1月20日に帯電付
着させ、そのまま放置して経過を観察したところ
昭和56年8月8日現在も付着したままで、なお継
続中であり、長時間の静電気付着力のあることが
確認された。
50μ thick film 900mm x 600mm and 200mm x 400
mm in size, with five colors printed on the surface, was rubbed against a vertically placed metal plate in an environment of temperature 5-28℃ and humidity 20-73%, and was electrostatically attached on January 20, 1981. When the adhesive was left as it was and the progress was observed, it was found that it was still attached as of August 8, 1982, and was continuing to adhere, confirming that it had a long-term electrostatic adhesive force.

Claims (1)

【特許請求の範囲】[Claims] 1 炭素数40〜60の有機ケトンを、塩化ビニルに
対して1〜3重量%の範囲で配合して、持続性静
電気付着力を付与したことを特徴とする塩化ビニ
ルフイルム。
1. A vinyl chloride film characterized in that it is blended with an organic ketone having 40 to 60 carbon atoms in a range of 1 to 3% by weight based on vinyl chloride to impart sustainable electrostatic adhesion.
JP13853781A 1981-09-04 1981-09-04 Vinyl chloride film having durable electrostatic attraction Granted JPS5840339A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP13853781A JPS5840339A (en) 1981-09-04 1981-09-04 Vinyl chloride film having durable electrostatic attraction
GB08225185A GB2108047B (en) 1981-09-04 1982-09-03 File for filing flat articles
DE19823232834 DE3232834A1 (en) 1981-09-04 1982-09-03 CARDBOARD, FILES, FOLDER OR THE LIKE FOR DEPOSITING FLAT OBJECTS

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13853781A JPS5840339A (en) 1981-09-04 1981-09-04 Vinyl chloride film having durable electrostatic attraction

Publications (2)

Publication Number Publication Date
JPS5840339A JPS5840339A (en) 1983-03-09
JPS6330940B2 true JPS6330940B2 (en) 1988-06-21

Family

ID=15224465

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13853781A Granted JPS5840339A (en) 1981-09-04 1981-09-04 Vinyl chloride film having durable electrostatic attraction

Country Status (1)

Country Link
JP (1) JPS5840339A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0780271B2 (en) * 1986-05-13 1995-08-30 米良 總一 Electrostatic adsorption sheet and film with printing surface

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5154150U (en) * 1974-10-21 1976-04-24

Also Published As

Publication number Publication date
JPS5840339A (en) 1983-03-09

Similar Documents

Publication Publication Date Title
US3964832A (en) Gel composition and adhesive stick
PL110670B1 (en) Method of making coatings and glue joints on the base of plastizol,on plastics
JPH0545612B2 (en)
US3764376A (en) Antistatic resinous compositions
JPS6330940B2 (en)
US2584340A (en) Reaction of organosilane with glycerine-dicarboxylic acid ester and dicarboxylic acid
US4011188A (en) Powdery coating composition
TW445286B (en) Radiation-polymerizable composition, film produced thereform and method for forming a coating on a substrate using the composition
US3218289A (en) Tetraalkyl pyromellitate plasticizers and plasticized polyvinyl compositions
JP3061150B2 (en) Aqueous dispersion composition, coating formed therefrom, and method for producing the same
JP3455671B2 (en) Antifouling paint composition
JPH02283722A (en) Manufacture of conductive polymer derived from 3-alkylthiophene, and conductive device containing said polymer
JPS6438474A (en) Stabilized synthetic polymer composition
US3219615A (en) Novel plasticized compositions
JPS6142947B2 (en)
JPS624761A (en) Coating composition
JPS6038415B2 (en) Methacrylic resin composition with excellent antistatic properties
JPS6129624B2 (en)
JPS5849574B2 (en) polypropylene composition
JPS6111976B2 (en)
JPH0326227B2 (en)
JP2910225B2 (en) Conductive resin composition
JPS5569635A (en) Polyolefin composition
JPS58170742A (en) Diisocyanate isomer mixture
US3973055A (en) Process of manufacture of dielectric recording media