JPH0251755B2 - - Google Patents
Info
- Publication number
- JPH0251755B2 JPH0251755B2 JP7411281A JP7411281A JPH0251755B2 JP H0251755 B2 JPH0251755 B2 JP H0251755B2 JP 7411281 A JP7411281 A JP 7411281A JP 7411281 A JP7411281 A JP 7411281A JP H0251755 B2 JPH0251755 B2 JP H0251755B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- stretching
- mimeograph
- paper according
- mimeograph paper
- 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
Links
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- -1 polyethylene Polymers 0.000 claims description 11
- 239000004698 Polyethylene Substances 0.000 claims description 8
- 229920000573 polyethylene Polymers 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- 230000000694 effects Effects 0.000 description 9
- 230000037303 wrinkles Effects 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 235000019645 odor Nutrition 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 239000006229 carbon black Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41N—PRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
- B41N1/00—Printing plates or foils; Materials therefor
- B41N1/24—Stencils; Stencil materials; Carriers therefor
- B41N1/246—Stencils; Stencil materials; Carriers therefor characterised by the electroconductive means or additives
Landscapes
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Printing Plates And Materials Therefor (AREA)
Description
本発明は電気記録謄写原紙に関する。
従来、電気記録謄写原紙用フイルムには、主と
してポリ塩化ビニルフイルムが用いられている
が、製版時に塩素系のガス例えば塩化ビニル、塩
化水素などが発生する為、人に不快な刺激臭を与
え、環境衛生上の問題があり、また製版装置の腐
食の問題があつた。
その為、塩素を含まない樹脂、例えばポリプロ
ピレン、ポリエチレン、ポリエステル、ポリスチ
レンなどを主成分とするフイルムなかでもフイル
ム成型性、強度などの点よりポリエチレンの適用
が多く試みられてきたが、例えばポリエチレンを
電気記録謄写原紙用フイルムとして使用すると、
ポリエチレンフイルムが印刷時に印刷インキ中に
含まれる油類によつて膨潤する為、フイルムに伸
びが発生し、印刷像が歪んだり、はなはだしくフ
イルムにシワが発生したりする欠点がある。この
様な欠点を改善する為、従来各種の提案がなされ
たが例えば耐油性の良い他の樹脂とブレンドす
る、エチレンと他の成分との共重合により耐油性
を向上させる、あるいは最初からポリエチレンに
油類を多量に配合しておくなどであり、いずれも
印刷時にフイルム伸びによる問題を生じさせない
為には、印刷インキによるフイルムの伸びが0.5
%以下、好ましくは0.3%以下でなければならず、
未だ実用に耐えるものは得られていないのが現状
である。
本発明はこの様な従来技術の欠点を解決したも
のであつて、製版時の不快臭、刺激臭がなく、か
つ印刷時のインキによるフイルムの伸びが殆んど
ないものである。
即ち、80〜105℃好ましくは90〜100℃の高温に
おいて導電性微粉末を含む、ポリオレフイン又は
ポリスチレンより選ばれた樹脂のフイルムを1.01
〜1.50倍、好ましくは1.05〜1.20倍の低倍率に延
伸し、冷却セツトしたものは収縮しようとする内
部歪(内部歪とは、歪が潜在化しているもので、
加熱することにより、或いは、溶剤、可塑剤など
と接触する事により、顕在化するものである。)
を保持し、印刷インキがフイルムに接触浸透する
時に、潜在していたその内部歪が発現し、印刷イ
ンキによる伸びと相殺されるものである。従つて
この様にして処理したフイルムを使用した電気記
録謄写原紙は製版時に不快臭、刺激臭がなく、し
かも印刷時の印刷インキによる伸びを0.3%以下
に抑える事が出来、印刷時の伸びの問題がない。
しかもフイルム用樹脂としては通常市販されてい
るポリオレフイン、ポリスチレンなどを使用する
事で足り、特殊な樹脂や高価な添加物を加える必
要もなく、経済的にも効果大なるものである。但
し、必要に応じ、本発明の効果を損わない限り、
通常樹脂に添加される添加物又はブレンド用樹脂
を若干量を用いてもよい。
延伸倍率を1.01〜1.50倍としたのは1.01倍未満
では効果が殆んどなく、また1.50倍以上では印刷
インキと接触した時に縮み過ぎる傾向にあり、か
つ延伸時にネツキングを生じる為である。又延伸
を安定的に行い、かつネツキングを起こさない為
には1.05〜1.20倍の延伸がより好ましい。さら
に、高温下において行う必要があるのは、常温以
下の温度で延伸を行う場合、本発明で実施する様
な低倍率では樹脂の弾性限界内に含まれる事があ
り、本発明の効果を充分に奏えない為である。
なお、延伸は一軸延伸でも本発明の効果を奏す
るが、二軸延伸の方がより好ましい。フイルムの
延伸は別工程で行い、公知の方法によつて導電台
紙に貼合しても又は延伸直後、導電台紙に貼合し
ても良い。
なお、フイルムの延伸は強度を高めるなどの為
に行われる場合もあるが、この様な場合は延伸倍
率が3〜10倍が通常の範囲であつて、本発明の目
的とする効果は奏し得ない。即ち、3−10倍の延
伸倍率では、収縮しようとする内部歪が過大であ
つて、印刷時にフイルム収縮が大きすぎる。更
に、製品のカールが起き易い。内部歪の残り易さ
から云えば、低圧法ポリエチレンが本発明に使用
する樹脂としては特に好適である。
本発明に用いる樹脂としては、ポリオレフイ
ン、例えば、低圧、高圧、又は中圧法ポリエチレ
ン、エチレン−酢ビコポリマー、ポリプロピレン
など、及び、スチレン樹脂、例えばポリスチレ
ン、スチレン−ブタジエン共重合体、スチレン−
メチルメタアクリレート共重合体など及びこれら
のブレンド物などが適用できる。また導電性微粉
末としてはカーボンブラツクなどの導電性無機粉
末を用いる事が出来る。
これらの配合例を挙げると次の如くである。
樹 脂 100重量部
導電性粉末 5−40重量部
また必要に応じ、本発明の樹脂フイルムは流動
パラフインなどの鉱物油類を含む事が出来るが、
その含有量が多いと内部歪の保持が困難となる為
本発明の効果を充分に奏する為にはその含有量は
導電性微粉末を含むフイルム中、5重量%以下好
ましくは2重量%以下(鉱物油自身も含まれたフ
イルムの全重量当り)が適当である。
又、本発明のフイルムの電気抵抗は好適には体
積固有抵抗106−1012Ω−cmである。又フイルム
の厚さは通常20〜40ミクロンが好ましい。
実施例1〜4、比較例1〜4
下記配合の樹脂原料を通常の方法により、イン
フレーシヨン法によつてフイルム化し、さらに延
伸したものを公知の方法によつて導電台紙と貼合
し、電気記録謄写原紙とした。これらを東京航空
計器(株)製「トーシヤフアツクスSH−600」で製版
したが、製版は鮮明であり、また製版時の不快
臭、刺激臭はなかつた。
さらにこの様にして製版したものを、輪転謄写
印刷機(デユプロ(株)製、「デユプロメイトM−
760」)にて中質紙を使用して各3000枚の印刷テス
トを行つた。その結果を後記の表に示す。
なお、ここでいうタテ方向とは謄写原紙を印刷
機に取り付けた状態において垂直方向であつて、
原反フイルムにおいては巾方向に該当する。又横
方向とはタテ方向に直角な方向であつて原反フイ
ルムにおける流れ方向に該当する。なお、通常の
輪転謄写印刷機の場合、その構造上、印刷時のフ
イルムのシワの発生については横方向の伸びが大
きく影響する。
また比較例として、同様にインフレーシヨン法
によつて作成したフイルムを延伸操作を加えずに
導電台紙に貼合した場合の結果、及び延伸倍率が
過大である場合の結果を併記した。
配合A低圧法ポリエチレン 100部
カーボンブラツク 30部
配合B低圧法ポリエチレン 100部
カーボンブラツク 20部
流動パラフイン 2.5部
TECHNICAL FIELD This invention relates to electrographic mimeograph paper. Conventionally, polyvinyl chloride film has been mainly used for electrical recording mimeograph films, but chlorine-based gases such as vinyl chloride and hydrogen chloride are generated during plate making, which gives off an unpleasant and irritating odor to people. There were problems with environmental hygiene and corrosion of the plate-making equipment. For this reason, many attempts have been made to use polyethylene in films based on chlorine-free resins such as polypropylene, polyethylene, polyester, and polystyrene due to its film formability and strength. When used as a recording mimeograph film,
Since the polyethylene film swells with the oils contained in the printing ink during printing, the film stretches, distorting the printed image, and causing excessive wrinkles on the film. In order to improve these drawbacks, various proposals have been made in the past, such as blending with other resins with good oil resistance, copolymerizing ethylene with other components to improve oil resistance, or using polyethylene from the beginning. In order to avoid problems caused by film elongation during printing, the elongation of the film due to printing ink must be 0.5.
% or less, preferably 0.3% or less,
At present, nothing suitable for practical use has yet been obtained. The present invention solves these drawbacks of the prior art, and has no unpleasant or irritating odor during plate making, and almost no elongation of the film due to ink during printing. That is, at a high temperature of 80 to 105°C, preferably 90 to 100°C, a film of a resin selected from polyolefin or polystyrene containing conductive fine powder is heated to 1.01°C.
Stretched to a low magnification of ~1.50 times, preferably 1.05 to 1.20 times, and cooled and set, internal strain tends to shrink (internal strain is latent strain,
It becomes apparent when heated or when it comes into contact with a solvent, plasticizer, etc. )
When the printing ink contacts and permeates the film, the latent internal strain is expressed and offset by the elongation caused by the printing ink. Therefore, the electrographic mimeograph paper using the film treated in this way has no unpleasant or irritating odor during plate making, and can suppress elongation due to printing ink to less than 0.3% during printing, resulting in less elongation during printing. there is no problem.
Furthermore, it is sufficient to use commercially available polyolefins, polystyrene, etc. as the resin for the film, and there is no need to add special resins or expensive additives, which is economically effective. However, if necessary, as long as it does not impair the effects of the present invention,
Some amount of additives or blending resins that are normally added to resins may be used. The stretching ratio is set to 1.01 to 1.50 times because if it is less than 1.01 times, there is almost no effect, and if it is more than 1.50 times, it tends to shrink too much when it comes into contact with printing ink, and netting occurs during stretching. Further, in order to perform the stretching stably and not to cause netting, it is more preferable to stretch the film by a factor of 1.05 to 1.20. Furthermore, it is necessary to carry out stretching at a high temperature, because when stretching is carried out at a temperature below room temperature, the effect of the present invention cannot be fully obtained because the low magnification as carried out in the present invention may be within the elastic limit of the resin. This is because it cannot be played. Note that although the effects of the present invention can be achieved even with uniaxial stretching, biaxial stretching is more preferable. The film may be stretched in a separate step and then laminated to the conductive mount by a known method, or the film may be laminated to the conductive mount immediately after stretching. Note that film stretching is sometimes carried out to increase strength, but in such cases, the stretching ratio is usually in the range of 3 to 10 times, and the desired effect of the present invention cannot be achieved. do not have. That is, at a stretching ratio of 3 to 10 times, the internal strain that tends to shrink is excessive, and the film shrinks too much during printing. Furthermore, the product tends to curl. Low-pressure polyethylene is particularly suitable as the resin used in the present invention in terms of its tendency to retain internal strain. The resins used in the present invention include polyolefins such as low-pressure, high-pressure, or medium-pressure polyethylene, ethylene-vinyl acetate copolymers, polypropylene, etc., and styrene resins such as polystyrene, styrene-butadiene copolymers, styrene-butadiene copolymers, etc.
Methyl methacrylate copolymers and blends thereof can be used. Further, as the conductive fine powder, conductive inorganic powder such as carbon black can be used. Examples of these formulations are as follows. Resin: 100 parts by weight Conductive powder: 5-40 parts by weight If necessary, the resin film of the present invention can contain mineral oils such as liquid paraffin.
If the content is too large, it becomes difficult to maintain internal strain, so in order to fully exhibit the effects of the present invention, the content should be 5% by weight or less, preferably 2% by weight or less ( (based on the total weight of the film including the mineral oil itself) is suitable. Further, the electrical resistance of the film of the present invention is preferably a volume resistivity of 10 6 -10 12 Ω-cm. The thickness of the film is usually preferably 20 to 40 microns. Examples 1 to 4, Comparative Examples 1 to 4 The following resin raw materials were made into a film by an inflation method using a conventional method, and the stretched film was laminated with a conductive mount by a known method. It was used as an electrical record mimeograph. These plates were made into plates using "Toshya Fox SH-600" manufactured by Tokyo Aircraft Instruments Co., Ltd., and the plates were clear and there were no unpleasant or irritating odors during plate making. Furthermore, the plate made in this way was printed on a rotary mimeograph machine (manufactured by Dupro Co., Ltd., "Dupromate M-
760''), we conducted a printing test of 3,000 sheets each using medium-quality paper. The results are shown in the table below. Note that the vertical direction here refers to the vertical direction when the mimeograph paper is attached to the printing machine.
For raw film, this corresponds to the width direction. The lateral direction is a direction perpendicular to the longitudinal direction, and corresponds to the flow direction in the original film. In addition, in the case of a normal rotary mimeograph printing machine, due to its structure, the generation of wrinkles in the film during printing is largely influenced by the elongation in the lateral direction. In addition, as a comparative example, the results when a film similarly prepared by the inflation method was laminated to a conductive mount without any stretching operation, and the results when the stretching ratio was too high are also shown. Blend A Low pressure polyethylene 100 parts Carbon black 30 parts Blend B Low pressure polyethylene 100 parts Carbon black 20 parts Liquid paraffin 2.5 parts
【表】
あつた。
以上の如く、通常の方法でフイルム化したもの
をそのまま使用した場合(比較例1〜3)は、印
刷時の伸びが大きく又、シワも発生し電気記録謄
写原紙としては実用され得ないが、各実施例に示
す如く適当な条件で低倍率で延伸したものは、伸
びも殆んどなく、シワの発生もない。
なお、実施例4に示す如く一軸延伸した場合は
延伸方向の伸びは改良されるが、その直角方向に
ついては逆に伸びがやや大となる傾向となる。
従つて、実施例4の如き一軸延伸でもシワの発
生は殆んどなく実用上、支障はないが、本発明の
効果をより完全なものとするには二軸延伸の方が
より好ましい。又比較例1及び2に示す如く、フ
イルム製膜時のブロー比を大とするなどしても印
刷時の伸びに対しては延伸の如き効果はなく、む
しろ伸びが大となる傾向にある。
また、この様にして延伸したフイルムを用いた
電気記録謄写原紙を60℃において2週間、及び常
温において1年間の経時変化テストを行つたが、
いずれの場合も延伸効果は充分保たれており、印
刷時の伸びによる問題はなかつた。[Table] Atsuta.
As mentioned above, when a film formed by a conventional method is used as it is (Comparative Examples 1 to 3), it stretches too much during printing and wrinkles occur, making it unusable as an electrical recording mimeograph paper. As shown in each example, those stretched at a low magnification under appropriate conditions have almost no elongation and no wrinkles. When uniaxially stretched as shown in Example 4, the elongation in the stretching direction is improved, but in the direction perpendicular to the stretching direction, the elongation tends to be slightly larger. Therefore, although uniaxial stretching as in Example 4 causes almost no wrinkles and poses no practical problem, biaxial stretching is more preferred in order to achieve the effects of the present invention more fully. Furthermore, as shown in Comparative Examples 1 and 2, even if the blowing ratio during film formation is increased, it does not have the same effect on elongation during printing as stretching does, but rather tends to increase elongation. In addition, an electrical recording mimeograph paper using the stretched film was subjected to aging tests at 60°C for two weeks and at room temperature for one year.
In all cases, the stretching effect was sufficiently maintained, and there were no problems caused by stretching during printing.
Claims (1)
チレン樹脂から選ばれた少くとも一つの樹脂から
なり、80−105℃において、1.01〜1.50倍の低倍
率延伸を施されたフイルムを使用したことを特徴
とする電気記録謄写原紙。 2 特許請求の範囲第1項において、該フイルム
がフイルム全重量の5重量%までの鉱物油を含む
ものであることを特徴とする電気記録謄写原紙。 3 特許請求の範囲第1項において、該フイルム
がフイルム全重量の2重量%までの鉱物油を含む
ものであることを特徴とする電気記録謄写原紙。 4 特許請求の範囲第1−3項のいずれかにおい
て、該樹脂が低圧法ポリエチレンであることを特
徴とする電気記録謄写原紙。 5 特許請求の範囲第1−4項のいずれかにおい
て、該低倍率延伸が二軸延伸であることを特徴と
する電気記録謄写原紙。[Claims] 1. A film made of at least one resin selected from polyolefin and styrene resin containing conductive fine powder, and stretched at a low magnification of 1.01 to 1.50 times at 80-105°C. Electric record mimeograph paper characterized by its use. 2. The electrographic mimeograph paper according to claim 1, characterized in that the film contains up to 5% by weight of mineral oil based on the total weight of the film. 3. The electrographic mimeograph paper according to claim 1, characterized in that the film contains up to 2% by weight of mineral oil based on the total weight of the film. 4. The electrical recording mimeograph paper according to any one of claims 1 to 3, characterized in that the resin is low-pressure polyethylene. 5. The electrographic mimeograph paper according to any one of claims 1 to 4, characterized in that the low-magnification stretching is biaxial stretching.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7411281A JPS57189896A (en) | 1981-05-19 | 1981-05-19 | Stencil paper for electric recording |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7411281A JPS57189896A (en) | 1981-05-19 | 1981-05-19 | Stencil paper for electric recording |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57189896A JPS57189896A (en) | 1982-11-22 |
| JPH0251755B2 true JPH0251755B2 (en) | 1990-11-08 |
Family
ID=13537785
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7411281A Granted JPS57189896A (en) | 1981-05-19 | 1981-05-19 | Stencil paper for electric recording |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS57189896A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59127797A (en) * | 1983-01-12 | 1984-07-23 | Sadami Ito | Electric discharge recording sheet |
| JPS59127796A (en) * | 1983-01-12 | 1984-07-23 | Sadami Ito | Electric discharge recording sheet |
| JPS59138489A (en) * | 1983-01-28 | 1984-08-08 | Sadami Ito | Electric discharge recording sheet |
| JPS59138491A (en) * | 1983-01-28 | 1984-08-08 | Sadami Ito | Electric discharge recording sheet |
| JPS59138490A (en) * | 1983-01-28 | 1984-08-08 | Sadami Ito | Electric discharge recording sheet |
-
1981
- 1981-05-19 JP JP7411281A patent/JPS57189896A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57189896A (en) | 1982-11-22 |
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