JPH01239041A - Production of laminated glass - Google Patents
Production of laminated glassInfo
- Publication number
- JPH01239041A JPH01239041A JP6321988A JP6321988A JPH01239041A JP H01239041 A JPH01239041 A JP H01239041A JP 6321988 A JP6321988 A JP 6321988A JP 6321988 A JP6321988 A JP 6321988A JP H01239041 A JPH01239041 A JP H01239041A
- Authority
- JP
- Japan
- Prior art keywords
- film
- glass
- thermoplastic synthetic
- laminated glass
- eva
- 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
- 239000005340 laminated glass Substances 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 11
- 239000011521 glass Substances 0.000 claims abstract description 23
- 239000002131 composite material Substances 0.000 claims abstract description 19
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 12
- 239000000057 synthetic resin Substances 0.000 claims abstract description 12
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 10
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 10
- 239000012965 benzophenone Substances 0.000 claims abstract description 6
- HHECSPXBQJHZAF-UHFFFAOYSA-N dihexyl hexanedioate Chemical compound CCCCCCOC(=O)CCCCC(=O)OCCCCCC HHECSPXBQJHZAF-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000003381 stabilizer Substances 0.000 claims abstract description 6
- 150000008366 benzophenones Chemical class 0.000 claims abstract description 5
- 239000004014 plasticizer Substances 0.000 claims abstract description 4
- MVWATEFMGRRVEL-UHFFFAOYSA-N tridecyl propanoate Chemical compound CCCCCCCCCCCCCOC(=O)CC MVWATEFMGRRVEL-UHFFFAOYSA-N 0.000 claims abstract description 4
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 abstract description 16
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 abstract description 10
- 229920001897 terpolymer Polymers 0.000 abstract description 8
- -1 polyethylene terephthalate Polymers 0.000 abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract description 4
- 229920002635 polyurethane Polymers 0.000 abstract description 4
- 239000004814 polyurethane Substances 0.000 abstract description 4
- 239000004952 Polyamide Substances 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 229920000515 polycarbonate Polymers 0.000 abstract description 2
- 239000004417 polycarbonate Substances 0.000 abstract description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract description 2
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 14
- 239000010410 layer Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 7
- 230000001070 adhesive effect Effects 0.000 description 7
- 230000032683 aging Effects 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000004831 Hot glue Substances 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 238000011074 autoclave method Methods 0.000 description 1
- JUPQTSLXMOCDHR-UHFFFAOYSA-N benzene-1,4-diol;bis(4-fluorophenyl)methanone Chemical compound OC1=CC=C(O)C=C1.C1=CC(F)=CC=C1C(=O)C1=CC=C(F)C=C1 JUPQTSLXMOCDHR-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical class C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000006076 specific stabilizer Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10009—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
- B32B17/10036—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising two outer glass sheets
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は異種材料からなる二層以上の複合フィルムをガ
ラス間に介在させて熱圧着するようにした建材、[]動
車用等の各種用途に使用される合わせカラスの製造方法
に関する。[Detailed Description of the Invention] [Industrial Field of Application] The present invention is applicable to various applications such as building materials, motor vehicles, etc. in which two or more layers of composite films made of different materials are interposed between glass and bonded under heat. This invention relates to a method for manufacturing laminated glass used for.
[従来の技術]
従来のこの種合わせガラスの製造方法は、ガラスとカラ
スの中間に一層のフィルム例えばPVB(ポリビニール
フチラール)、ポリウレタン、その他の種々の合成樹脂
フィルムを入れ、オートクレーブによる圧着法または熱
圧着による方法により製造されていた。オートクレーブ
による圧着法は例えば圧力5〜10Kg/cm2.温度
80〜100°Cの条件下にオートクレーブ内にガラス
を入れ、ガラスとガラスの中間に上記フィルムを入れ、
さらに圧力10〜l S K g、/cm”て時間15
〜20分をかけて圧着して接合する方法である。このオ
ートクレーブによる圧着法では中間に介在させるフィル
ムとしてPVBか通常使用される。また熱圧着による方
法では中間に介在させるフィルムとしてEVA (エチ
レンビニルアセテートコポリマー)またはEVAグラフ
トターポリマーか通常使用される。[Prior Art] The conventional method for manufacturing this type of laminated glass is to insert a layer of film, such as PVB (polyvinyl phthalate), polyurethane, or other various synthetic resin films, between the glass and the glass, and use a pressure bonding method using an autoclave. Alternatively, they were manufactured by thermocompression bonding. In the pressure bonding method using an autoclave, for example, the pressure is 5 to 10 kg/cm2. Glass is placed in an autoclave at a temperature of 80 to 100°C, and the film is placed between the glasses,
Furthermore, the pressure is 10~l S K g,/cm" and the time is 15
This method takes about 20 minutes to press and bond. In this pressure bonding method using an autoclave, PVB is usually used as an intervening film. In addition, in the method using thermocompression bonding, EVA (ethylene vinyl acetate copolymer) or EVA graft terpolymer is usually used as the intervening film.
[発明が解決しようとする課題]
L記従来の合わせガラスの製造方法では中間に介在させ
るフィルムが一層であるために機械的強度か十分てない
ばかりでなくガラスとの密着性も未だ十分てないという
難点があった。またフィルム自体も経時的に老化したり
、あるいは太陽光線の透過等による紫外線の影響により
フィルムの劣化か進行して合わせガラスの耐久性の点で
問題かあった。ざらにオートクレーブによる圧着法によ
った場合、装置か大がかりとなり、工程も面倒でありコ
スト高となる等の欠点を有し・ていた。[Problem to be solved by the invention] L: In the conventional laminated glass manufacturing method, since the film interposed in the middle is a single layer, not only the mechanical strength is insufficient, but also the adhesion to the glass is still insufficient. There was a problem. In addition, the film itself ages over time, or the film deteriorates due to the influence of ultraviolet rays due to the transmission of sunlight, etc., causing problems in terms of the durability of the laminated glass. In the case of the crimping method using an autoclave, the apparatus is large-scale, the process is troublesome, and the cost is high.
本発明は上記の点に鑑みてなされたもので、その目的と
するところはフィルム自体の強度を増大させるとともに
老化の防1Fを図り、かつガラスとの密着性を増大させ
ることにより合わせガラスとして機械的強度の増大を図
り、しかも容易な圧着方式にて安価に量産てきるように
した合わせガラスの製造方法を提供することにある。The present invention has been made in view of the above points, and its purpose is to increase the strength of the film itself, prevent aging, and increase adhesion to glass, so that it can be used as laminated glass. It is an object of the present invention to provide a method for manufacturing laminated glass that increases the mechanical strength and that can be mass-produced at low cost using an easy pressure bonding method.
[課題を解決するための子役]
本発明に係る合わせカラスの製造方法は可塑剤としてト
リエチレングリコール・2・エーテル酪酸またはジ−N
−ヘキシルアジペートを、安定剤としてl−リゾシルプ
ロピオネート、ベンゾフェノン類をそれぞれ含有せしめ
た異種の熱u(塑性合成樹脂フィルムを組合わせて二以
上りの複合フィルムを形成した後1.核複合フィルムを
ガラス間に介在させて熱圧着させる構成としたものであ
る。[Child role for solving the problem] The method for producing laminated glass according to the present invention uses triethylene glycol-2-etherbutyric acid or di-N as a plasticizer.
- Hexyl adipate containing l-lysosylpropionate and benzophenones as stabilizers, respectively. The structure is such that the film is interposed between the glasses and bonded under heat.
本発明てOf塑剤としてトリエチレンクリコール・2・
エーテル酪酸またはジ−N−ヘキシルアジペートを使用
することとしたのは、熱可塑性合成樹脂フィルムのり塑
性を促進させ、ガラスとの密着性を増大させるるともに
熱や光等に起因するフィルムの老化を防止するようにす
る等のためである。また安定剤としてトリデシルプロピ
オネート、ベンゾフェノン類を使用することとしたのは
、熱可塑性合成樹脂フィルムて紫外線を吸収し該フィル
ムの劣化を防止して合わせガラスの耐久性を向ヒさせる
ためである。異種の熱ijT塑性合成樹脂フィルムの組
合わせに当たっては相溶性の樹脂を選定し密着性を良好
にする必要かある。異種の樹脂を組合わせることにより
相互の補完作用か働きフィルムの機械的強度か増すこと
となる。フィルムを形成する熱可塑性合成樹脂としては
PVB、ポリウレタン、EVA、EVAクラフトターポ
リマー、変性エチレン酢酸ビニールコポリマー、PE5
(ポリエーテルスル
リエーテルエーテルケトン)、ポリアミド、ポリカーボ
ネート、ポリエチレンテレフタレート、ポリブチレンテ
レフタレート、ポリベンゾイル、ポリアセタール、ポリ
フェニルサルファイド等の樹脂か使用される。熱可塑性
合成樹脂フィルムの組合わせ例として、例えば三層の場
合は異なる樹脂をA.B.CとするとA/B/Cといっ
た異種同士の組合わせやB/A/Bといったサントイウ
チ状の組合わせ態様か考えられ、四層の場合は異なる樹
脂をA.B.C.DとするとA/B/C/Dといった全
部異種の組合わせやA/B/A/Bといった二種の樹脂
を交互に組合わせたりあるいはA/B/’A/C,A/
B/C/A等の組合わせ態様か考えられる。いずれにし
ても、ガラスと接合する樹脂は密着性の良い樹脂を選ぶ
ことか肝要てあり、また熱膨張率もカラスのそれと近似
したものを選定する必要かある。In the present invention, triethylene glycol 2.
The reason for using etherbutyric acid or di-N-hexyl adipate is to promote the plasticity of the thermoplastic synthetic resin film, increase its adhesion to glass, and prevent aging of the film caused by heat, light, etc. This is for the purpose of preventing this. In addition, we decided to use tridecylpropionate and benzophenones as stabilizers because the thermoplastic synthetic resin film absorbs ultraviolet rays, prevents the film from deteriorating, and improves the durability of the laminated glass. be. When combining different types of thermal ijT plastic synthetic resin films, it is necessary to select compatible resins to ensure good adhesion. By combining different types of resins, the mechanical strength of the film increases due to their mutually complementary effects. Thermoplastic synthetic resins that form the film include PVB, polyurethane, EVA, EVA kraft terpolymer, modified ethylene vinyl acetate copolymer, and PE5.
Resins such as (polyether sulfur ether ether ketone), polyamide, polycarbonate, polyethylene terephthalate, polybutylene terephthalate, polybenzoyl, polyacetal, and polyphenyl sulfide are used. As an example of a combination of thermoplastic synthetic resin films, for example, in the case of three layers, different resins are used in A. B. If C is a combination of different types such as A/B/C or a combination of different types such as B/A/B, in the case of four layers, different resins may be used as A. B. C. If D is a combination of all different types such as A/B/C/D, or a combination of two types of resins such as A/B/A/B, or A/B/'A/C, A/
A possible combination such as B/C/A is possible. In any case, it is important to select a resin that has good adhesion for bonding with the glass, and it is also necessary to select a resin that has a coefficient of thermal expansion similar to that of the glass.
上記二層以上のフィルムを作成するには、ホットメルト
または接着剤を使用してトライラミネートして作る。例
えばEVAクラフトターポリマーフィルムとPVBフィ
ルムをEVAホットメルト接着剤でトライラミネートし
て複合フィルムを作る。この複合フィルムの厚さは建材
用の場合、0、67mmで、そのうちEVAフィルムは
0.271m11とするのが標準である。自動車用の場
合、例えば三層の複合フィルムではその中心フィルムの
厚さは0.25〜0.31で、該中心フィルムを挟んだ
両側の例えばEVAフィルムは0625〜0、3mmと
する。To create a film with two or more layers, the film is tri-laminated using hot melt or adhesive. For example, EVA kraft terpolymer film and PVB film are tri-laminated with EVA hot melt adhesive to create a composite film. The thickness of this composite film for building materials is 0.67 mm, of which the standard thickness for EVA film is 0.271 m11. In the case of automobiles, for example, in the case of a three-layer composite film, the thickness of the center film is 0.25 to 0.31 mm, and the thickness of the EVA films on both sides of the center film is 0.625 to 0.3 mm.
北記の方法により得られた複合フィルムは、ガラスとガ
ラスの間に介在させて、これを高温圧力機にセットする
。この時の条件は、温度を100〜120℃とし圧力を
10〜15Kg/c112に設定し、時間は15〜20
分間この状態で熱圧着する。こうして高温、高圧をかけ
ることにより複合フィルムは軟化し、可塑性を増しガラ
スと複合フィルムとの間にある気泡か除去されるととも
に該ガラスとの密着性か高まることとなる。The composite film obtained by Kita's method is placed between glasses and set in a high-temperature pressure machine. The conditions at this time are a temperature of 100 to 120℃, a pressure of 10 to 15Kg/c112, and a time of 15 to 20℃.
Heat and press in this state for a minute. In this way, by applying high temperature and high pressure, the composite film becomes soft, increases its plasticity, removes air bubbles between the glass and the composite film, and improves its adhesion to the glass.
上記一定の時間熱圧着した後、上記高温圧力機から取出
しこれを所定時間冷却して所望の合わせガラスを得る。After thermocompression bonding for the predetermined time, it is taken out from the high temperature pressure machine and cooled for a predetermined time to obtain the desired laminated glass.
[発明の効果]
本発明は上記の説明から判るように、nf塑剤としてI
−リエチレンクリコール・2・エーテル酪酸またはジー
N−ヘキシルアジペートを、安定剤としてトリデシルプ
ロピオネ−1〜、ベンゾフェノン類をそれぞれ含有せし
めた異種の熱可塑性合成樹脂フィルムを組合わせて二層
以上の複合フィルムを形成した後、該複合フィルムをガ
ラス間に介在させて熱圧着した合わせガラスの製造方法
であるから、上記複合フィルムの可塑性か増し、ガラス
との密着性か良くなり複合フィルムの老化防止か図られ
る。従って、フィルムの多層化とあいまって合わせガラ
スとしての機械的強度か増す等JIS、AS、ECE等
の各種の規格に適合する製品か得られるという優れた効
果を奏する。また熱可塑性合成樹脂フィルムに上記する
特定の安定剤を含有せしめることとしたので、該フィル
ムで紫外線を良く吸収し、フィルムの劣化が防tl=さ
れ合わせガラスの耐久性か向上するという特有の効果を
奏する。しかも筒便な熱圧着方式により合わせガラスを
製造することかできるので、安価に大量生産することか
出来、オートクレーブ方式と同等の圧着強度の合わせガ
ラスか得られるという利点を有する。[Effect of the invention] As can be seen from the above explanation, the present invention uses I as an nf plastic agent.
- Two or more layers of thermoplastic synthetic resin films containing lyethylene glycol 2-etherbutyric acid or di-N-hexyl adipate, tridecylpropionone-1 or benzophenones as stabilizers, respectively, are combined. This is a laminated glass manufacturing method in which a composite film is formed, and then the composite film is interposed between glasses and bonded by thermocompression, so the plasticity of the composite film is increased, the adhesion with the glass is improved, and the aging of the composite film is prevented. or planned. Therefore, in combination with the multilayering of the film, the mechanical strength of the laminated glass is increased, and excellent effects can be obtained in that a product conforming to various standards such as JIS, AS, ECE, etc. can be obtained. In addition, since the thermoplastic synthetic resin film contains the above-mentioned specific stabilizer, the film has the unique effect of absorbing ultraviolet rays well, preventing film deterioration, and improving the durability of laminated glass. play. Moreover, since the laminated glass can be manufactured by a convenient thermocompression bonding method, it has the advantage that it can be mass-produced at low cost and that laminated glass with the same bonding strength as the autoclave method can be obtained.
[実施例]
■PVBフィルムの製造 (重陽部)PVB樹
脂(Chang Chun製) 100ジー
N−ヘキシルアジペート 50(CH3)
4(COOCsHt:+)2トリデシルプロピオネート
3上記混合物をバンバリーミキサ−に
て上方混合し、これをつオミングローJしにかけて練っ
た。次いで、逆り詩聖カレンターロールを通した後、ク
リーンクロールに通した。そして厚さを0.2〜0.7
1■に調整してフィルムを製造した。[Example] ■Manufacture of PVB film (Duyang part) PVB resin (manufactured by Chang Chun) 100G N-hexyl adipate 50 (CH3)
4 (COOCsHt:+)2 tridecylpropionate 3 The above mixture was mixed upward in a Banbury mixer, and kneaded by passing it through an Omingrow J. Next, it was passed through a reverse Shisei Calendar roll, and then passed through a clean crawl. And the thickness is 0.2~0.7
A film was produced by adjusting the concentration to 1.
■EVAグラフトターポリマーフィルムの製造EVAグ
ラフトターポリマー 100ジ−N−ヘキシルア
ジペート lOトリデシルプロピオネート
3ベンゾフエノンマーク
0.2PVBフイルムと同様な方法で行ない、その厚さ
を0.2〜0.3mmに調整してフィルムを製造した。■Manufacture of EVA graft terpolymer film EVA graft terpolymer 100 di-N-hexyl adipate 10 tridecyl propionate 3 benzophenone mark
A film was manufactured in the same manner as the 0.2PVB film, with the thickness adjusted to 0.2 to 0.3 mm.
■ホットメルトタイプの接着剤
エチレン酢酸ヒニールボリマ−100
ジーN−ヘキシルアジペート 5トリテ
シルブロピオネート 2ベンンフエノンマ
ーク 0. 1」二記混合物を70〜12
0°Cに加熱し上方混合した後冷却し接着剤とした。■Hot-melt type adhesive Ethylene acetate vinyl polymer-100 Di-N-hexyl adipate 5 Tritesyl propionate 2 Bennephenone mark 0. 1" mixture of 70-12
The mixture was heated to 0°C, mixed upwards, and then cooled to form an adhesive.
尚、上記PVBフィルム及びEVAクラフトターポリマ
ーフィルムの使用に代えて、ポリウレタンフィルム、P
ES、PEEK等のフィルムを使用する場合は、接着剤
として、二液ポリウレタン接着剤を使用する。In addition, instead of using the above-mentioned PVB film and EVA craft terpolymer film, polyurethane film, P
When using a film such as ES or PEEK, a two-component polyurethane adhesive is used as the adhesive.
この二液接着剤の成分は次の通りてあった。The components of this two-component adhesive were as follows.
Desmolin N 100Des
100Des 176 40コロネ
ート L 20酢酸エチル
20トロール
40MEK
20MIBK 2
0この二液接着剤の場合はロールコーチ、イング方式で
コーティングして1〜ライラミネートをする。Desmolin N 100Des
100Des 176 40Coronate L 20Ethyl acetate
20 trolls
40MEK
20MIBK 2
0 In the case of this two-component adhesive, coat with the roll coach and ing method and 1 to lye laminate.
上記■のPVBフィルムの両面に上記■のホットメルト
タイプの接着剤を塗布した後、上記■のEVAプラント
ターポリマーフィルムを該■のPVBフィルムの両面に
当てドライラミネート機を使用してラミネート1ノ三層
の複合フィルムを製造した。次に上記三層の複合フィル
ムをガラスとガラスの間にセットした状態で高温圧力機
にセットし熱圧着した。この時の温度は100〜120
℃て、圧力は10〜15Kg/cm2で、時間は15〜
20分てあった。上記熱圧着終了後、冷却して取出し所
望する合わせガラスを得た。After applying the hot-melt adhesive described in (2) above to both sides of the PVB film in (2) above, apply the EVA plant terpolymer film in (2) above to both sides of the PVB film in (1) and laminate one layer using a dry laminating machine. A three-layer composite film was produced. Next, the three-layer composite film was placed between glasses and placed in a high-temperature pressure machine to be bonded by thermocompression. The temperature at this time is 100-120
℃, the pressure is 10~15Kg/cm2, and the time is 15~15Kg/cm2.
It was 20 minutes. After the thermocompression bonding was completed, the glass was cooled and taken out to obtain a desired laminated glass.
得られた合わせガラスは、複合フィルムとガラスとの密
着性か高く、自動市川、建材用等として機械的強度や耐
久性に優れたものか得られた。The obtained laminated glass had high adhesion between the composite film and the glass, and had excellent mechanical strength and durability for use in automatic products, building materials, etc.
Claims (1)
酸またはジ−N−ヘキシルアジペートを、安定剤として
トリデシルプロピオネート、ベンゾフェノン類をそれぞ
れ含有せしめた異種の熱可塑性合成樹脂フィルムを組合
わせて二層以上の複合フィルムを形成した後、該複合フ
ィルムをガラス間に介在させて熱圧着したことを特徴と
する合わせガラスの製造方法。Two or more layers of different thermoplastic synthetic resin films containing triethylene glycol 2-etherbutyric acid or di-N-hexyl adipate as a plasticizer and tridecylpropionate and benzophenones as stabilizers. 1. A method for manufacturing laminated glass, which comprises forming a composite film, and then interposing the composite film between glasses and bonding them by thermocompression.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6321988A JPH01239041A (en) | 1988-03-18 | 1988-03-18 | Production of laminated glass |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6321988A JPH01239041A (en) | 1988-03-18 | 1988-03-18 | Production of laminated glass |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01239041A true JPH01239041A (en) | 1989-09-25 |
Family
ID=13222879
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6321988A Pending JPH01239041A (en) | 1988-03-18 | 1988-03-18 | Production of laminated glass |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01239041A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0447964A2 (en) * | 1990-03-22 | 1991-09-25 | BASF Aktiengesellschaft | Shaped articles of aromatic polyetherketones stabilized against UV radiation and process for preparing them |
EP0449063A2 (en) * | 1990-03-22 | 1991-10-02 | BASF Aktiengesellschaft | UV stabilised aromatic polyethersulphone shaped bodies and production process |
JP2002046217A (en) * | 2000-08-02 | 2002-02-12 | Bridgestone Corp | Film-reinforced glass |
WO2002049982A1 (en) * | 2000-12-18 | 2002-06-27 | Bridgestone Corporation | Film-reinforced glasses |
JP2003176159A (en) * | 2002-10-04 | 2003-06-24 | Bridgestone Corp | Composite resin film |
-
1988
- 1988-03-18 JP JP6321988A patent/JPH01239041A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0447964A2 (en) * | 1990-03-22 | 1991-09-25 | BASF Aktiengesellschaft | Shaped articles of aromatic polyetherketones stabilized against UV radiation and process for preparing them |
EP0449063A2 (en) * | 1990-03-22 | 1991-10-02 | BASF Aktiengesellschaft | UV stabilised aromatic polyethersulphone shaped bodies and production process |
JP2002046217A (en) * | 2000-08-02 | 2002-02-12 | Bridgestone Corp | Film-reinforced glass |
WO2002049982A1 (en) * | 2000-12-18 | 2002-06-27 | Bridgestone Corporation | Film-reinforced glasses |
US7332216B2 (en) | 2000-12-18 | 2008-02-19 | Bridgestone Corporation | Film-reinforced glasses |
EP1346962A4 (en) * | 2000-12-18 | 2008-12-31 | Bridgestone Corp | Film-reinforced glasses |
JP2003176159A (en) * | 2002-10-04 | 2003-06-24 | Bridgestone Corp | Composite resin film |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6423170B1 (en) | Thermoplastic interlayer film | |
DE3789629T3 (en) | Packaging oxygen barrier layer | |
CN100566994C (en) | A kind of paper plastic glue-free composite bidirectional stretching polypropylene film and preparation method thereof | |
SE8305253D0 (en) | PASTEURIZABLE COOK-IN SHRINK MOVIE | |
JPH049672B2 (en) | ||
EP0951499A1 (en) | Thermoplastic interlayer film | |
US4911984A (en) | Laminated glazing unit | |
JP3057646B2 (en) | Acrylate compound and laminate using the acrylate compound | |
JPH01239041A (en) | Production of laminated glass | |
CA1061973A (en) | Matt and scratch-resistant films and process for their manufacture | |
DE3773266D1 (en) | METHOD FOR PRODUCING COMPOSITE DISCS. | |
CS78491A2 (en) | Multi-layer foil and method of its production | |
JPS5841178B2 (en) | Method for manufacturing composite film | |
US5035851A (en) | Method of making very high barrier film | |
KR102127555B1 (en) | Polypropylene-based hotmelt film having excellent heat adhesion with aluminum metallizing film | |
AU604788B2 (en) | Very high barrier film | |
KR200166707Y1 (en) | Vehicle ceiling material | |
JPS57207025A (en) | Manufacture of laminated and stretched film | |
DE3875011D1 (en) | MULTI-LAYER FILM WITH HIGH IMPACT AND STRENGTH RESISTANCE, METHOD FOR THEIR PRODUCTION AND THEIR USE. | |
EP1562746B1 (en) | Heat shrinkable bioriented multilayer film with gas barrier properties | |
CN107160780A (en) | A kind of manufacture method of doubling glass | |
KR200440685Y1 (en) | A cheap price film for paper coating | |
JPH08319140A (en) | Production of laminated glass | |
JPS58147353A (en) | Laminated panel | |
JPS5917628Y2 (en) | composite sheet |