JPH04255322A - Moistureproof film - Google Patents
Moistureproof filmInfo
- Publication number
- JPH04255322A JPH04255322A JP3100588A JP10058891A JPH04255322A JP H04255322 A JPH04255322 A JP H04255322A JP 3100588 A JP3100588 A JP 3100588A JP 10058891 A JP10058891 A JP 10058891A JP H04255322 A JPH04255322 A JP H04255322A
- Authority
- JP
- Japan
- Prior art keywords
- temp
- film
- moisture
- sheet
- proof film
- 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.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 14
- 239000011347 resin Substances 0.000 claims abstract description 14
- 230000009477 glass transition Effects 0.000 claims abstract description 8
- 238000001125 extrusion Methods 0.000 claims abstract description 5
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920001577 copolymer Polymers 0.000 claims abstract description 4
- 238000003851 corona treatment Methods 0.000 claims description 5
- 229920006027 ternary co-polymer Polymers 0.000 claims description 3
- CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 claims description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
- 229920001897 terpolymer Polymers 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims 1
- 238000007789 sealing Methods 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 5
- 238000009998 heat setting Methods 0.000 abstract description 3
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 6
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/911—Cooling
- B29C48/9135—Cooling of flat articles, e.g. using specially adapted supporting means
- B29C48/914—Cooling of flat articles, e.g. using specially adapted supporting means cooling drums
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
- B29C48/08—Flat, e.g. panels flexible, e.g. films
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
- B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
- B29C48/865—Heating
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Electroluminescent Light Sources (AREA)
- Laminated Bodies (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は防湿性に優れたエレクト
ロルミネッセンス素子(以下,EL素子)の被覆封止用
フィルムに関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a film for covering and sealing electroluminescent devices (hereinafter referred to as EL devices) with excellent moisture resistance.
【0002】0002
【従来の技術】近年、液晶表示体のバックライト、照明
、表示灯などにEL素子が多く利用されているが、EL
素子は吸湿により劣化し易く、性能が低下するという欠
点がある。そこで、これを防止するために、従来より未
延伸の三フッ化塩化エチレン樹脂(以下、PCTFE)
フィルムで被覆封止して使用されている。しかしながら
、EL素子の寿命は防湿性が不十分なために起こる吸湿
劣化に大きく左右されるため、さらなる防湿性の向上が
望まれていた。[Prior Art] In recent years, EL elements have been widely used in backlights, lighting, indicator lights, etc. of liquid crystal displays.
The device has the disadvantage of being easily deteriorated by moisture absorption, resulting in a decrease in performance. Therefore, in order to prevent this, conventional unstretched trifluorochloroethylene resin (hereinafter referred to as PCTFE)
It is used covered and sealed with a film. However, since the life of an EL element is greatly affected by moisture absorption deterioration caused by insufficient moisture resistance, further improvement in moisture resistance has been desired.
【0003】0003
【発明が解決しようとする課題】本発明の目的とすると
ころは、防湿性が著しく優れたEL素子の被覆封止用フ
ィルムを提供するにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a film for covering and sealing an EL element that has extremely excellent moisture resistance.
【0004】0004
【課題を解決するための手段】本発明は、PCTFEま
たはその共重合体を溶融押し出し法により、シート状に
した後、ガラス転移温度より50〜140℃高い温度で
一軸延伸し、延伸温度より高い温度でヒートセットした
ことを特徴とする防湿性フィルムである。[Means for Solving the Problems] The present invention involves forming PCTFE or a copolymer thereof into a sheet by melt extrusion, and then uniaxially stretching the sheet at a temperature 50 to 140°C higher than the glass transition temperature. This is a moisture-proof film that is heat-set.
【0005】本発明に用いられるPCTFEとは三フッ
化塩化エチレン単独重合体またはそれと共重合可能な他
の単量体との共重合体であり、他の単量体の含有率は防
湿性からみて20重量%以下であることが好ましく、さ
らには5重量%以下であることが好ましい。また、PC
TFEの重合度については、ASTM 1430に規
定されたZ.S.T.(Zero strengh
time)を目安とした場合、機械的強度、シート成
型性からみて150〜400秒であることが好ましい。[0005] PCTFE used in the present invention is a trifluorochloroethylene homopolymer or a copolymer with other monomers copolymerizable with it, and the content of other monomers is determined depending on moisture resistance. It is preferably 20% by weight or less, more preferably 5% by weight or less. Also, PC
Regarding the degree of polymerization of TFE, Z. S. T. (Zero strength
time) is preferably 150 to 400 seconds in terms of mechanical strength and sheet formability.
【0006】本発明ではシート状に溶融押し出しする際
、冷却工程で結晶化を抑えることがシートの透明性、延
伸適性の点で好ましく、このためには樹脂温度を250
〜350℃の溶融状態でダイより押し出し、表面温度を
10〜100℃に制御した冷却ロール上で冷却すればよ
い。In the present invention, when melt extruding into a sheet, it is preferable to suppress crystallization in the cooling process from the viewpoint of sheet transparency and stretching suitability.
It may be extruded from a die in a molten state at ~350°C and cooled on a cooling roll whose surface temperature is controlled at 10-100°C.
【0007】この様にして得られたシートをガラス転移
温度より50〜140℃高い温度で一軸延伸することに
より、防湿性の非常に優れたフィルムが得られる。延伸
温度がガラス転移温度より50℃高い温度未満であると
均一な延伸が困難であり、ガラス転移温度より140℃
高い温度より高い場合は延伸の効果が小さくなる。延伸
方向は延伸適性からみて縦方向が好ましく、延伸倍率は
1.5倍から4倍に延伸することで効果が得られる。こ
の場合の延伸後のフィルム厚みは100〜300μmで
あることが好ましい。また延伸後に延伸温度より高い温
度でヒートセットすることにより、接着性樹脂を積層す
る際のフィルムの熱変形を防止することができる。[0007] By uniaxially stretching the sheet thus obtained at a temperature 50 to 140°C higher than the glass transition temperature, a film with extremely excellent moisture resistance can be obtained. If the stretching temperature is less than 50°C higher than the glass transition temperature, uniform stretching will be difficult;
If the temperature is higher than that, the effect of stretching will be reduced. The stretching direction is preferably the longitudinal direction in view of stretching suitability, and effects can be obtained by stretching the stretching ratio from 1.5 times to 4 times. In this case, the film thickness after stretching is preferably 100 to 300 μm. Further, by heat setting the film at a temperature higher than the stretching temperature after stretching, it is possible to prevent thermal deformation of the film when laminating the adhesive resin.
【0008】以上の工程で得られたフィルムをEL素子
の被覆封止に使用するには端部を接着することが必要で
あるが、PCTFEフィルムの場合、表面処理を行わな
いと接着が困難であり、プラズマ処理、コロナ処理、ス
パッタ処理などの方法がとられているがコスト面からみ
て、コロナ処理が好ましい。コロナ処理された面にエチ
レン・グリシジルメタクリレート・酢酸ビニル3元共重
合体(以下、EGV樹脂)を積層することにより良好な
ヒートシール性を持った接着層がえられるがさらに低温
でヒートシール性を付与するためにEGV樹脂上にエチ
レン・エチルアクリレート・無水マレイン酸3元共重合
体(以下、EEM樹脂)を積層することが好ましい。[0008] In order to use the film obtained by the above process for sealing the EL element, it is necessary to adhere the edges, but in the case of PCTFE film, adhesion is difficult unless surface treatment is performed. Although methods such as plasma treatment, corona treatment, and sputter treatment have been used, corona treatment is preferable from a cost standpoint. By laminating ethylene-glycidyl methacrylate-vinyl acetate terpolymer (hereinafter referred to as EGV resin) on the corona-treated surface, an adhesive layer with good heat-sealing properties can be obtained. It is preferable to laminate an ethylene/ethyl acrylate/maleic anhydride ternary copolymer (hereinafter referred to as EEM resin) on the EGV resin in order to provide the resin.
【0009】[0009]
【実施例】《実施例1》PCTFE(ガラス転移温度5
2℃ Z.S.T.300秒)を設定温度340℃の
ダイから溶融状で押し出し、30℃に設定した冷却ロー
ル上で冷却して厚さ600μmのシートにした後、この
シートをシート温度150℃で縦方向に3倍に延伸して
200μmのフィルムにし、180℃でヒートセットし
た。更に、このフィルムの片面をコロナ処理して、ぬれ
指数48dyn/cmまで活性化した後、この面にEG
V樹脂(ボンドファースト7B 住友化学工業製)を
溶融押し出しにより、積層して加圧ロールで押圧しなが
ら冷却してフィルムを得た[Example] <<Example 1>> PCTFE (glass transition temperature 5
2℃ Z. S. T. 300 seconds) is extruded in molten form through a die with a set temperature of 340°C, cooled on a cooling roll set at 30°C to form a sheet with a thickness of 600 μm, and this sheet is then tripled in the longitudinal direction at a sheet temperature of 150°C. The film was stretched to 200 μm and heat set at 180°C. Furthermore, one side of this film was treated with corona to activate it to a wetting index of 48 dyn/cm, and then EG was applied to this side.
V resin (Bond First 7B, manufactured by Sumitomo Chemical Industries) was laminated by melt extrusion and cooled while being pressed with a pressure roll to obtain a film.
【0010】《実施例2》実施例1で得られたフィルム
のEGV樹脂層上にEEM樹脂(ボンダインAX806
4 住友化学工業製)を溶融押し出しにより、積層し
て加圧ロールで押圧しながら冷却してフィルムを得た。<<Example 2>> EEM resin (Bondine AX806) was applied on the EGV resin layer of the film obtained in Example 1.
4 (manufactured by Sumitomo Chemical Industries) were laminated by melt extrusion and cooled while being pressed with a pressure roll to obtain a film.
【0011】《比較例1》PCTFEを溶融押し出しし
、厚さ200μmのフィルム上にした後、実施例1と同
様にコロナ処理後、EGV樹脂を積層してフィルムを得
た。<Comparative Example 1> PCTFE was melt-extruded to form a film having a thickness of 200 μm, and after corona treatment in the same manner as in Example 1, an EGV resin was laminated to obtain a film.
【0012】《比較例2》比較例1で得られたフィルム
のEGV樹脂層上に実施例2と同様にしてEEM樹脂を
積層してフィルムを得た。Comparative Example 2 An EEM resin was laminated on the EGV resin layer of the film obtained in Comparative Example 1 in the same manner as in Example 2 to obtain a film.
【0013】《比較例3》実施例1でコロナ処理を施さ
ないこと以外は同じ方法でフィルムを得た。Comparative Example 3 A film was obtained in the same manner as in Example 1 except that the corona treatment was not performed.
【0014】以上の5種類のフィルムについて防湿性、
ヒートシール性を下記に示す測定方法で測定した結果を
表1に示す。(測定方法)防湿性 :6
0℃95%RHの雰囲気中で、水蒸気透過率を測定した
。ヒートシール性:2枚のフィルムの接着層面を重ね合
わせて、温度を2条件で、圧力10kg/cm23秒間
圧着し、180゜剥離試験を行った。[0014] Regarding the above five types of films, moisture resistance,
Table 1 shows the results of heat sealing properties measured using the measurement method shown below. (Measurement method) Moisture resistance: 6
Water vapor transmission rate was measured in an atmosphere of 0° C. and 95% RH. Heat-sealability: The adhesive layer surfaces of two films were placed one on top of the other, and a 180° peel test was performed by pressing the films together under two conditions of temperature and pressure of 10 kg/cm for 23 seconds.
【0015】[0015]
【表1】[Table 1]
【0016】[0016]
【発明の効果】本発明のフイルムは著しく防湿性に優れ
ており、EL素子用フイルムとして好適であ。[Effects of the Invention] The film of the present invention has extremely excellent moisture resistance and is suitable as a film for EL devices.
Claims (4)
その共重合体を溶融押し出し法により、シート状にした
後、ガラス転移温度より50〜140℃高い温度で一軸
延伸し、延伸温度より高い温度でヒートセットしたこと
を特徴とする防湿性フィルム。Claim 1: A trifluorochloroethylene resin or a copolymer thereof is formed into a sheet by melt extrusion, and then uniaxially stretched at a temperature of 50 to 140°C higher than the glass transition temperature, and then stretched at a temperature higher than the stretching temperature. A moisture-proof film characterized by being heat-set.
をコロナ処理したことを特徴とする防湿性フィルム。2. A moisture-proof film, characterized in that the surface of the moisture-proof film according to claim 1 has been subjected to corona treatment.
ナ処理された面に、エチレン・グリシジルメタクリレー
ト・酢酸ビニル3元共重合体を積層したことを特徴とす
る防湿性フィルム。3. A moisture-proof film, characterized in that an ethylene-glycidyl methacrylate-vinyl acetate terpolymer is laminated on the corona-treated surface of the moisture-proof film according to claim 2.
レン・グリシジルメタクリレート・酢酸ビニル3元共重
合体層上にエチレン・エチルアクリレート・無水マレイ
ン酸3元共重合体を積層したことを特徴とする防湿性フ
ィルム。4. The moisture-proof film according to claim 3, wherein an ethylene/ethyl acrylate/maleic anhydride ternary copolymer is laminated on the ethylene/glycidyl methacrylate/vinyl acetate ternary copolymer layer. Moisture-proof film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3100588A JPH04255322A (en) | 1991-02-06 | 1991-02-06 | Moistureproof film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3100588A JPH04255322A (en) | 1991-02-06 | 1991-02-06 | Moistureproof film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04255322A true JPH04255322A (en) | 1992-09-10 |
Family
ID=14278043
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3100588A Pending JPH04255322A (en) | 1991-02-06 | 1991-02-06 | Moistureproof film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04255322A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0684123A3 (en) * | 1994-05-25 | 1996-02-07 | Kureha Chemical Ind Co Ltd | Stretched polychlorotrifluoroethylene film, process for production thereof and packaged product using the film. |
WO1999002328A1 (en) * | 1997-07-09 | 1999-01-21 | Toray Industries, Inc. | Method of producing thermoplastic resin film and apparatus for producing the same |
JP2002237381A (en) * | 2001-02-09 | 2002-08-23 | Nagase Inteko Kk | Organic electroluminescence element |
US6907945B2 (en) | 2001-05-24 | 2005-06-21 | Ki-Soo Kim | Wheel chair |
US8980430B2 (en) | 2006-08-28 | 2015-03-17 | Frank J. Colombo | PCTFE film with extrusion coating of EVA or EVA with UV absorbers |
-
1991
- 1991-02-06 JP JP3100588A patent/JPH04255322A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0684123A3 (en) * | 1994-05-25 | 1996-02-07 | Kureha Chemical Ind Co Ltd | Stretched polychlorotrifluoroethylene film, process for production thereof and packaged product using the film. |
WO1999002328A1 (en) * | 1997-07-09 | 1999-01-21 | Toray Industries, Inc. | Method of producing thermoplastic resin film and apparatus for producing the same |
US6221301B1 (en) | 1997-07-09 | 2001-04-24 | Toray Industries, Inc. | Method of producing thermoplastic resin films and apparatus for producing the same |
JP2002237381A (en) * | 2001-02-09 | 2002-08-23 | Nagase Inteko Kk | Organic electroluminescence element |
US6907945B2 (en) | 2001-05-24 | 2005-06-21 | Ki-Soo Kim | Wheel chair |
US8980430B2 (en) | 2006-08-28 | 2015-03-17 | Frank J. Colombo | PCTFE film with extrusion coating of EVA or EVA with UV absorbers |
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