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JPH0431396B2 - - Google Patents
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JPH0431396B2 - - Google Patents

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Publication number
JPH0431396B2
JPH0431396B2 JP59262993A JP26299384A JPH0431396B2 JP H0431396 B2 JPH0431396 B2 JP H0431396B2 JP 59262993 A JP59262993 A JP 59262993A JP 26299384 A JP26299384 A JP 26299384A JP H0431396 B2 JPH0431396 B2 JP H0431396B2
Authority
JP
Japan
Prior art keywords
marking
base material
marking material
seconds
thickness
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 - Lifetime
Application number
JP59262993A
Other languages
Japanese (ja)
Other versions
JPS61141477A (en
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 filed Critical
Priority to JP59262993A priority Critical patent/JPS61141477A/en
Priority to PCT/US1985/002442 priority patent/WO1986003767A1/en
Priority to KR1019860700562A priority patent/KR930010441B1/en
Priority to EP86900474A priority patent/EP0203996A1/en
Priority to CA000497556A priority patent/CA1282287C/en
Publication of JPS61141477A publication Critical patent/JPS61141477A/en
Publication of JPH0431396B2 publication Critical patent/JPH0431396B2/ja
Granted legal-status Critical Current

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Classifications

    • GPHYSICS
    • G09EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09FDISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F3/00Labels, tag tickets, or similar identification or indication means; Seals; Postage or like stamps
    • G09F3/02Forms or constructions
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/26Porous or cellular plastics
    • GPHYSICS
    • G09EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09FDISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F3/00Labels, tag tickets, or similar identification or indication means; Seals; Postage or like stamps
    • G09F3/02Forms or constructions
    • G09F2003/023Adhesive
    • G09F2003/0236Permeability

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Theoretical Computer Science (AREA)
  • Laminated Bodies (AREA)
  • Adhesive Tapes (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Glass Compositions (AREA)
  • General Preparation And Processing Of Foods (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、屋外看板、2輪車用ガソリンタン
ク、車両外板等に貼着して用いられる装飾標示用
のマーキング材料の改良に関する。さらに詳しく
は、貼着される被着体から気体(アウトガス)が
発生しても、剥れ、ふくれ等が生じない通気性の
あるマーキング材料の改良に関する。 〔従来の技術〕 従来の通気性のあるマーキング材料を第3図乃
至第7図を用いて説明する。 第3図に示すマーキング材料は、基材1に粘着
剤層2を積層後、機械的もしくは化学的に空気抜
きの孔3を設けた構成となつている。 次に第4図に示すマーキング材料は、基材1
が、通気性のある繊維質のものから形成された構
成になつている。 次に第5図に示すマーキング材料は、基材1と
粘着剤層2との間に発泡体、紙、繊維質等の通気
性のある多孔質層4を設けた構成となつている
(例えば実開昭59−90980号公報)。 次に第6図に示すマーキング材料は、粘着剤層
2を発泡多孔質で形成した構成となつている。 さらに第7図に示すように、通気性のないマー
キング材料であるが、基材1を極端に厚く(約
250μm以上)し、基材の強度を上げ、アウトガス
を封じ込めようとした構成のものがあつた。 〔発明が解決しようとする問題点〕 しかしながら、前記第3図に示したマーキング
材料は、マーキング材料の上に所望のマーキング
(通常オフセツト、グラビア、スクリーン等の印
刷法や、ロールコート、ナイフコート等のコーテ
イング方で形成される)を施した場合、孔径が大
きすぎると表面状態が悪く光沢も不良で実用に供
し得ない。また孔径が小さすぎるとマーキング形
成時に孔がつぶされ通気性が劣り、好ましくない
ので、孔径の加工が非常に難しく、作業性も悪
い。 前記第4図に示したマーキング材料は、基材の
機械的強度が低いので破損しやすく、基材の表面
平滑性も劣り光沢をもつマーキングを得ることは
困難であつた。 次に前記第5図に示したマーキング材料は、多
孔質層の機械的強度が低いので層破壊を生じやす
いばかりでなく、多量のガスが発生する被着体へ
貼着した場合(例えば成形したてのRIMバンパ
ーやFRP板への貼着、ガソリンの充填されたポ
リエチレン容器への貼着)、ガスを外部に逃がし
きれず、ふくれ等を生じる。 次に前記第6図に示したマーキング材料は、接
着強度が低く被着体から剥れやすいばかりでな
く、多量のガスを外部に逃がしきれず、上記第5
図に示したマーキング材料と同様、ふくれ等を生
じる。 さらに前記第7図に示したマーキング材料は、
被着体へ貼着後、短時間では問題ないが、時間が
経過するほどかえつて大きなふくれ、剥れ等が生
じ問題である。 そこで本発明は、外観状態の良好なマーキング
を施すことができ、多量のガスが発生する被着体
へ貼着しても、剥れ、ふくれ等の問題が生じない
マーキング材料を提供することを目的とする。 〔問題点を解決するための手段〕 本発明のマーキング材料を第1図により説明す
ると、基材1は、平均孔径0.2μm〜50μm、通気
量はJIS P8117ガーレ式での測定値が2秒/100
c.c.〜120秒/100c.c.、厚さ20μm以上の連続多孔質
プラスチツクフイルムから形成されており、基材
1の片面には粘着剤層2が積層された構成となつ
ている。なお粘着剤層2の面にさらに剥離材を積
層し、マーキング材料の取扱いを容易にすること
もできる。 本発明のマーキング材料に用いられる基材は平
均孔径が0.2μm〜50μm、通気量は2秒/100c.c.〜
120秒/100c.c.(JIS P8117ガーレ式)、厚さ20μm
以上の連続多孔質プラスチツクフイルムである。
平均孔径が0.2μmに満たない場合には、マーキン
グ材料の上に形成されるマーキングにより孔が塞
がれ、通気性が劣り好ましくなく、50μmを超え
ると、マーキングの外観不良が生じ、実用に供し
得ない。光沢のあるマーキングを施すことがで
き、かつ、有効な通気性を得るためには10〜
20μmの範囲が特に好ましい。 次に通気料(JIS P8117ガーレ式)が2秒/
100c.c.を超えると(この単位(秒/100c.c.)では数
値が小さい程通気量が大であるので、超えるとは
数値的には小さくなることを意味する)基材の表
面平滑性が劣ることになりマーキングの外観不良
が生ずることになり、120秒/100c.c.未満である
(この場合は数値的には大きくなる)と通気性が
劣り、好ましくない。基材1の強度と通気性能を
考慮すると10秒/100c.c.〜50秒/100c.c.がより好ま
しい。 次に、第2図に示したようにマーキング材料の
表面全面にマーキング6を施した場合を考える
と、マーキング材料表面の孔は、マーキング6
(インク、クリヤー等)により多数塞がれるため
通気性が劣ることになる。このため、被着体より
生じるアウトガスAはマーキング材料の端部切断
面からも外部へ抜けることになる。従つて、基材
の厚みが20μmに満たないと、マーキング材料の
端部切断面積は小さくなり、通気性が劣り好まし
くない。特に安定した通気性と、マーキング材料
の経済性、加工性等を考慮すると基材の厚さは
60μm〜200μmの範囲が好ましい。上記の如き本
発明の基材は、特公昭59−5327号公報等に開示の
如く、焼結法、混合抽出法、相分離法、延伸法の
各方法により製造することができ、塩化ビニル、
ポリエチレン、アクリル、ウレタン、ポリプロピ
レン等の汎用性のある熱可塑性プラスチツク材料
を使用することができる。 次に本発明で用いられる粘着剤としては、積層
される基材と、貼着される被着体との接着力を得
ることができれば良く、また通常用いられる範囲
の塗布厚みがあれば何等加工をほどこさずとも充
分通気性があるので、アクリル系、ゴム系、シリ
コン系等の汎用の粘着剤を用いることができる。 〔実施例〕 以下本発明のマーキング材料を実施例によりさ
らに詳細に説明する。 例 1 塩化ビニルオルガノゾル(住友スリーエム社
製)に、エチルアルコールを20重量%加え、
800rpm×15分プロペラミキサーで攪拌し、キヤ
ステイング法を用い、相分離法により連続多孔質
の基材を形成した。該基材に30μmdry厚みのアク
リル系粘着剤(住友スリーエム社製)と、剥離材
を積層し、マーキング材料を形成した。前記マー
キング材料の基材表面に住友スリーエム社製〓
3900シリーズインクで全面にスクリーン印刷を
し、乾燥後この上にさらに住友スリーエム社製
GA−1クリヤーを約10μmdry厚みとなるよう同
様に塗布し、マーキングを施した。このマーキン
グ材を用いて以下の試験を行なつた。 (a) ブリスター試験 サンコープラスチツク社製広口ポリエチレン
ビン500c.c.にガソリンを充填、密閉し、該ビン
表面に上記マーキング材を貼着する。25℃、65
%RHに1ケ月放置後、ブリスターの発生の有
無を目視で確認した。 成形後24時間以内の自動車ウレタンバンパー
RIM成形品(三ツ星ベルト(株)製)に上記マー
キング材を貼着する。これを80℃、48時間オー
ブン中に入れ、ブリスターの発生の有無を目視
で確認した。 、の試験とも以下の基準で評価した。 ◎…ブリスターの発生全くなし ○…微小のブリスターの発生 △…部分的にブリスターの発生 ×…全面にブリスターの発生 (b) 外観状態 前記(a)と同様のマーキング材のマーキング表面
を目視で確認し、以下の評価基準とした。 ◎…非常に光沢あり。 ○…光沢あり。 △…艶消状。(外観状態良好) ×…表面がガサガサして光沢がなく、インクの
のりも悪い。 (外観状態不良) (c) 表面光沢 前記(a)と同様のマーキング材のマーキング表面
の60°における光沢度を測定した。(日本電色工業
社製デジタル光沢度計VG−2P−D3を使用した) 以下、実施例と比較例の評価結果を表1〜表3
に示す。 表1は基材の厚み70μm、通気量30秒/100c.c.で
平均孔径を変化させた場合の評価結果を示す。 表2は基材の厚み70μm、平均孔径10μmで通気
量を変化させた場合の評価結果を示す。 表3は基材の平均孔径10μm、通気量30秒/100
c.c.で厚みを変化させた場合の評価結果を示す。
[Industrial Field of Application] The present invention relates to improvements in marking materials for decorative signs used by being attached to outdoor signboards, gasoline tanks for two-wheeled vehicles, vehicle exterior panels, and the like. More specifically, the present invention relates to an improvement in a breathable marking material that does not peel off, blister, etc. even if gas (outgas) is generated from an adherend to which it is attached. [Prior Art] A conventional breathable marking material will be explained with reference to FIGS. 3 to 7. The marking material shown in FIG. 3 has a structure in which an adhesive layer 2 is laminated on a base material 1, and then air vent holes 3 are mechanically or chemically provided. Next, the marking material shown in FIG.
However, it is constructed from a breathable fibrous material. Next, the marking material shown in FIG. 5 has a structure in which an air-permeable porous layer 4 made of foam, paper, fiber, etc. is provided between a base material 1 and an adhesive layer 2 (for example, Utility Model Publication No. 59-90980). Next, the marking material shown in FIG. 6 has a structure in which the adhesive layer 2 is made of foamed porous material. Furthermore, as shown in FIG.
250 μm or more), the strength of the base material was increased, and the structure was designed to contain outgas. [Problems to be Solved by the Invention] However, the marking material shown in FIG. If the pore size is too large, the surface condition will be poor and the gloss will be poor, making it impossible to put it to practical use. Furthermore, if the hole diameter is too small, the hole will be crushed during marking formation, resulting in poor air permeability, which is undesirable, making it extremely difficult to process the hole diameter and resulting in poor workability. The marking material shown in FIG. 4 is easily damaged because the mechanical strength of the base material is low, and the surface smoothness of the base material is also poor, making it difficult to obtain a glossy marking. Next, the marking material shown in Fig. 5 has a low mechanical strength of the porous layer, so it is not only easy to cause layer destruction, but also when attached to an adherend that generates a large amount of gas (for example, a molded (adhering to other RIM bumpers or FRP boards, or adhering to polyethylene containers filled with gasoline), the gas cannot escape to the outside, causing blisters, etc. Next, the marking material shown in FIG.
Similar to the marking material shown in the figure, blistering occurs. Furthermore, the marking material shown in FIG.
There is no problem for a short time after adhesion to the adherend, but the longer time passes, the more problems arise as blistering, peeling, etc. occur. SUMMARY OF THE INVENTION Therefore, the present invention aims to provide a marking material that can provide markings with a good appearance and that does not cause problems such as peeling or blistering even when applied to an adherend that generates a large amount of gas. purpose. [Means for Solving the Problems] The marking material of the present invention will be explained with reference to FIG. 1. The base material 1 has an average pore diameter of 0.2 μm to 50 μm, and an air flow rate of 2 seconds/2 seconds/minute as measured by the JIS P8117 Gurley method. 100
It is made of a continuous porous plastic film having a length of cc~120 seconds/100 c.c. and a thickness of 20 μm or more, and has a structure in which an adhesive layer 2 is laminated on one side of a base material 1. Note that a release material may be further laminated on the surface of the adhesive layer 2 to facilitate handling of the marking material. The base material used in the marking material of the present invention has an average pore diameter of 0.2 μm to 50 μm, and an air flow rate of 2 seconds/100 c.c.
120 seconds/100c.c. (JIS P8117 Gurley type), thickness 20μm
This is a continuous porous plastic film as described above.
If the average pore diameter is less than 0.2 μm, the marking formed on the marking material will block the pores, resulting in poor air permeability, which is undesirable. If it exceeds 50 μm, the appearance of the marking will be poor, making it unsuitable for practical use. I don't get it. 10~10 to be able to apply glossy markings and to obtain effective ventilation.
A range of 20 μm is particularly preferred. Next, the ventilation (JIS P8117 Gurley type) is set for 2 seconds/
If it exceeds 100c.c. (in this unit (seconds/100c.c.), the smaller the number, the larger the airflow rate, so exceeding means that it is numerically smaller), the surface smoothness of the base material If it is less than 120 seconds/100 c.c. (in this case, the numerical value is large), the air permeability will be poor, which is not preferable. Considering the strength and air permeability of the base material 1, 10 seconds/100 c.c. to 50 seconds/100 c.c. is more preferable. Next, considering the case where the marking 6 is applied to the entire surface of the marking material as shown in FIG. 2, the holes on the surface of the marking material are
(ink, clear, etc.), resulting in poor air permeability. Therefore, the outgas A generated from the adherend escapes to the outside from the cut end surface of the marking material as well. Therefore, if the thickness of the base material is less than 20 μm, the end cut area of the marking material will be small, resulting in poor air permeability, which is not preferable. In particular, considering stable air permeability, economy of marking materials, processability, etc., the thickness of the base material is
A range of 60 μm to 200 μm is preferred. The base material of the present invention as described above can be manufactured by a sintering method, a mixed extraction method, a phase separation method, and a stretching method, as disclosed in Japanese Patent Publication No. 59-5327, etc.
Versatile thermoplastic materials such as polyethylene, acrylic, urethane, polypropylene, etc. can be used. Next, the adhesive used in the present invention should be able to obtain adhesive strength between the base material to be laminated and the adherend to which it is attached, and can be processed in any way as long as it has a coating thickness within the commonly used range. Since the adhesive has sufficient air permeability even without the use of adhesives, general-purpose adhesives such as acrylic, rubber, and silicone adhesives can be used. [Example] The marking material of the present invention will be explained in more detail below with reference to Examples. Example 1 Add 20% by weight of ethyl alcohol to vinyl chloride organosol (manufactured by Sumitomo 3M),
The mixture was stirred at 800 rpm for 15 minutes using a propeller mixer, and a continuous porous base material was formed using a casting method and a phase separation method. A marking material was formed by laminating a 30 μm dry thick acrylic adhesive (manufactured by Sumitomo 3M) and a release material on the base material. Manufactured by Sumitomo 3M Co., Ltd. on the surface of the base material of the marking material
Screen print the entire surface with 3900 series ink, and after drying, add Sumitomo 3M's ink on top of this.
GA-1 clear was applied in the same manner to a dry thickness of about 10 μm, and markings were applied. The following tests were conducted using this marking material. (a) Blister test A 500 c.c. wide-mouth polyethylene bottle manufactured by Sanko Plastics Co., Ltd. is filled with gasoline, sealed, and the above marking material is affixed to the surface of the bottle. 25℃, 65
After being left at %RH for one month, the presence or absence of blistering was visually confirmed. Automotive urethane bumper within 24 hours after molding
Attach the above marking material to the RIM molded product (manufactured by Mitsuboshi Belting Co., Ltd.). This was placed in an oven at 80°C for 48 hours, and the presence or absence of blisters was visually confirmed. Both tests were evaluated using the following criteria. ◎...No blisters at all ○...Minute blisters occur △...Blisters partially occur ×...Blisters occur on the entire surface (b) Appearance condition Visually check the marking surface of the same marking material as in (a) above The following evaluation criteria were used. ◎…Very shiny. ○…Glossy. △…Matte. (Good appearance) ×...The surface is rough and lacks gloss, and the ink does not adhere well. (Poor appearance) (c) Surface gloss The gloss at 60° of the marking surface of the same marking material as in (a) above was measured. (A digital gloss meter VG-2P-D3 manufactured by Nippon Denshoku Kogyo Co., Ltd. was used.) Below, the evaluation results of Examples and Comparative Examples are shown in Tables 1 to 3.
Shown below. Table 1 shows the evaluation results when the average pore diameter was varied at a base material thickness of 70 μm and an air flow rate of 30 seconds/100 c.c. Table 2 shows the evaluation results when the base material thickness was 70 μm, the average pore diameter was 10 μm, and the ventilation amount was varied. Table 3 shows the average pore diameter of the base material: 10 μm, air flow rate: 30 seconds/100
The evaluation results are shown when the thickness is changed by cc.

【表】 尚、前記第3図、5図、6図、7図に示した従
来のマーキング材料はブリスター試験及びで
いづれもXの結果であり、前記第4図に示した従
来のマーキング材料は外観状態でXの結果であつ
た。
[Table] The conventional marking materials shown in FIGS. 3, 5, 6, and 7 above all gave X results in the blister test, and the conventional marking materials shown in FIG. The result was X in terms of appearance.

【表】【table】

【表】 例 2 ポリプロピレン連続多孔質フイルム(住友スリ
ーエム社製)を基材として用い、該基材表面を塩
素化ポリプロピレン(東洋化成工業社製)でプラ
イマ処理し、前記実施例(例1)と同様にアクリ
ル系粘着剤と剥離材を積層して、マーキング材料
を形成した。さらに前記(例1)と同様にマーキ
ングを施し、前記ブリスター試験(もも同様
な結果のためまとめて1つとして記述した)、外
観状態、表面光沢を評価した。実施例と比較例の
評価結果を表4〜表6に示す。 表4は基材の厚み80μm、通気量38秒/100c.c.で
平均孔径を変化させた場合の評価結果を示す。 表5は基材の厚み80μm、平均孔径3.2μmで通
気量を変化させた場合の評価結果を示す。表6は
基材の平均孔径3.2μm、通気量38秒/100c.c.で厚
みを変化させた場合の評価結果を示す。
[Table] Example 2 A polypropylene continuous porous film (manufactured by Sumitomo 3M) was used as a base material, and the surface of the base material was treated with a primer with chlorinated polypropylene (manufactured by Toyo Kasei Kogyo Co., Ltd.), and the same as in the above example (Example 1) was used. Similarly, a marking material was formed by laminating an acrylic adhesive and a release material. Furthermore, markings were applied in the same manner as in the above (Example 1), and the blister test (described as one single product due to similar results), appearance, and surface gloss were evaluated. The evaluation results of Examples and Comparative Examples are shown in Tables 4 to 6. Table 4 shows the evaluation results when the average pore diameter was varied at a base material thickness of 80 μm and an air flow rate of 38 seconds/100 c.c. Table 5 shows the evaluation results when the base material thickness was 80 μm, the average pore diameter was 3.2 μm, and the air flow rate was varied. Table 6 shows the evaluation results when the average pore diameter of the base material was 3.2 μm, the air flow rate was 38 seconds/100 c.c., and the thickness was varied.

【表】【table】

【表】【table】

〔発明の効果〕〔Effect of the invention〕

以上説明した通り、本発明のマーキング材料の
基材は、平均孔径0.2〜50μm、通気量2秒/100
c.c.〜120秒/100c.c.、厚み20μm以上の連続多孔質
プラスチツクフイルムにより形成されているの
で、艶消状から光沢のある外観状態の良好なマー
キングを施すことができる。さらに、たとえ全面
にマーキングが施されていても充分に通気性のあ
るマーキング材を得ることができる。また、基材
と粘着剤層との間に、多孔質層もないので、層破
壊も生じることのない、強度の高いマーキング材
を提供できる。
As explained above, the base material of the marking material of the present invention has an average pore diameter of 0.2 to 50 μm and an air flow rate of 2 seconds/100 μm.
cc ~ 120 seconds/100 c.c., and is formed from a continuous porous plastic film with a thickness of 20 μm or more, so markings with a good appearance ranging from matte to glossy can be made. Furthermore, even if the entire surface is marked, a marking material with sufficient air permeability can be obtained. Further, since there is no porous layer between the base material and the adhesive layer, it is possible to provide a marking material with high strength that does not cause layer destruction.

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

第1図は本発明のマーキング材料を示す断面
図、第2図は本発明のマーキング材料にマーキン
グを施し、被着体に貼着したときの断面図、第3
図〜第7図は従来の通気性マーキング材料を示す
断面図である。 1……基材、2……粘着剤層、3……孔、4…
…多孔質層、5……被着体、6……マーキング。
Fig. 1 is a cross-sectional view showing the marking material of the present invention, Fig. 2 is a cross-sectional view of the marking material of the present invention applied with markings and attached to an adherend, and Fig. 3 is a cross-sectional view showing the marking material of the present invention.
7 are cross-sectional views showing conventional air permeable marking materials. 1... Base material, 2... Adhesive layer, 3... Hole, 4...
...Porous layer, 5...Adherent, 6...Marking.

Claims (1)

【特許請求の範囲】[Claims] 1 基材に粘着剤層を積層して成るマーキング材
料において;該基材が、平均孔径0.2μm〜50μm、
通気量2秒/100c.c.〜120秒/100c.c.、厚さ20μm以
上の連続多孔質プラスチツクフイルムにより形成
されていることを特徴とするマーキング材料。
1 In a marking material formed by laminating an adhesive layer on a base material; the base material has an average pore size of 0.2 μm to 50 μm,
A marking material characterized by being formed of a continuous porous plastic film having an air flow rate of 2 seconds/100 c.c. to 120 seconds/100 c.c. and a thickness of 20 μm or more.
JP59262993A 1984-12-14 1984-12-14 Marking material Granted JPS61141477A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP59262993A JPS61141477A (en) 1984-12-14 1984-12-14 Marking material
PCT/US1985/002442 WO1986003767A1 (en) 1984-12-14 1985-12-10 Marking materials
KR1019860700562A KR930010441B1 (en) 1984-12-14 1985-12-10 Marking materials
EP86900474A EP0203996A1 (en) 1984-12-14 1985-12-10 Marking materials
CA000497556A CA1282287C (en) 1984-12-14 1985-12-13 Marking material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59262993A JPS61141477A (en) 1984-12-14 1984-12-14 Marking material

Publications (2)

Publication Number Publication Date
JPS61141477A JPS61141477A (en) 1986-06-28
JPH0431396B2 true JPH0431396B2 (en) 1992-05-26

Family

ID=17383405

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59262993A Granted JPS61141477A (en) 1984-12-14 1984-12-14 Marking material

Country Status (5)

Country Link
EP (1) EP0203996A1 (en)
JP (1) JPS61141477A (en)
KR (1) KR930010441B1 (en)
CA (1) CA1282287C (en)
WO (1) WO1986003767A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2011648A1 (en) * 1989-03-31 1990-09-30 Dennis O. Falaas Permeable application tape and application transfer articles comprising same
JPH0416479U (en) * 1990-05-31 1992-02-10
US5626955A (en) * 1994-04-04 1997-05-06 Minnesota Mining And Manufacturing Company Microparticle-containing pressure sensitive adhesive tape
US5512612A (en) * 1994-04-04 1996-04-30 Minnesota Mining And Manufacturing Company Pressure sensitive adhesive employing a water-dispersible polymer and articles made there from
JPWO2002067592A1 (en) * 2001-02-21 2004-06-24 ソニー株式会社 Data transmission method and apparatus
JP4125875B2 (en) * 2001-04-13 2008-07-30 日東電工株式会社 Sealant for electrical and electronic equipment
JP4308606B2 (en) * 2003-08-26 2009-08-05 日東電工株式会社 Label and vented housing using the same
US9752061B2 (en) * 2012-09-28 2017-09-05 Lintec Corporation Adhesive sheet and method for manufacturing adhesive sheet

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3854581A (en) * 1972-04-10 1974-12-17 Monarch Marking Systems Inc Pressure-sensitive material and supporting material combination
US4169184A (en) * 1973-05-07 1979-09-25 Joseph Pufahl Adhesive coated impregnated polyurethane foam
FR2288626A1 (en) * 1974-10-23 1976-05-21 Seilib Document markers anchored by pressure on adhesive loaded foam - for use on or to anchor various surfaces without damage to the substrate

Also Published As

Publication number Publication date
WO1986003767A1 (en) 1986-07-03
CA1282287C (en) 1991-04-02
KR930010441B1 (en) 1993-10-25
EP0203996A1 (en) 1986-12-10
JPS61141477A (en) 1986-06-28
KR870700085A (en) 1987-02-28

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