JPS59174546A - Mirror - Google Patents
MirrorInfo
- Publication number
- JPS59174546A JPS59174546A JP58238727A JP23872783A JPS59174546A JP S59174546 A JPS59174546 A JP S59174546A JP 58238727 A JP58238727 A JP 58238727A JP 23872783 A JP23872783 A JP 23872783A JP S59174546 A JPS59174546 A JP S59174546A
- Authority
- JP
- Japan
- Prior art keywords
- electron beam
- curing
- layer
- mirror
- coating
- 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
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/08—Mirrors
- G02B5/0816—Multilayer mirrors, i.e. having two or more reflecting layers
- G02B5/085—Multilayer mirrors, i.e. having two or more reflecting layers at least one of the reflecting layers comprising metal
- G02B5/0858—Multilayer mirrors, i.e. having two or more reflecting layers at least one of the reflecting layers comprising metal the reflecting layers comprising a single metallic layer with one or more dielectric layers
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/36—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal
- C03C17/38—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating being a metal at least one coating being a coating of an organic material
-
- G02B1/105—
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/08—Mirrors
- G02B5/0808—Mirrors having a single reflecting layer
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/08—Mirrors
- G02B5/0816—Multilayer mirrors, i.e. having two or more reflecting layers
- G02B5/085—Multilayer mirrors, i.e. having two or more reflecting layers at least one of the reflecting layers comprising metal
- G02B5/0858—Multilayer mirrors, i.e. having two or more reflecting layers at least one of the reflecting layers comprising metal the reflecting layers comprising a single metallic layer with one or more dielectric layers
- G02B5/0866—Multilayer mirrors, i.e. having two or more reflecting layers at least one of the reflecting layers comprising metal the reflecting layers comprising a single metallic layer with one or more dielectric layers incorporating one or more organic, e.g. polymeric layers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Surface Treatment Of Glass (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Optical Elements Other Than Lenses (AREA)
- Mirrors, Picture Frames, Photograph Stands, And Related Fastening Devices (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は透明ガラスシートの裏面に反射層を適用し、該
層の上に1層あるいは数層の保護層を被覆することを特
徴とする鏡の製造法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a mirror, characterized in that a reflective layer is applied to the back side of a transparent glass sheet, and one or several protective layers are coated on top of said layer. be.
最も通常の鏡製造法においては、透明ガラスシートの裏
面に通常銀の反射層が被覆せられる。In the most common mirror manufacturing process, the back side of a transparent glass sheet is coated with a reflective layer, usually silver.
この銀層は銅層で被覆されさらに銅層が塗料あるいはフ
ェスで塗布される。塗料層は下の金属層の腐食ならびに
摩耗を保護する。This silver layer is covered with a copper layer, which is then applied with paint or face. The paint layer protects the underlying metal layer from corrosion and wear.
かかる方法の主な欠点は保護塗料層が乾燥するのにある
程度時間がかかり、従って新しく製造された鏡を塗料が
湿潤状態にある間裏面が他のものと接触しないように貯
蔵しておかねはならぬ点にある。これは鏡の大規模な生
産にあたって、非常に大きな貯蔵空間を必要とするため
都合の悪い点である。The main disadvantage of such a method is that the protective paint layer takes some time to dry, so it is necessary to store newly manufactured mirrors so that the back side does not come into contact with other objects while the paint is still wet. It's in the wrong place. This is inconvenient for large-scale production of mirrors, as it requires a very large storage space.
従来用いられている通常の製造法においては、溶媒の蒸
発により保護層が固化する。そのため大規模の生産にお
いて溶媒蒸発で工場大気の汚染という問題を生じる。ま
たこういった鏡を加熱しないメ充分に迅速な乾燥は達成
されない。In conventional manufacturing methods, the protective layer is solidified by evaporation of the solvent. Therefore, in large-scale production, solvent evaporation poses a problem of polluting the factory atmosphere. Also, sufficiently rapid drying is not achieved without heating these mirrors.
本発明の一つの目的はこういった欠点のない鏡の製造法
を提供するにある。One object of the invention is to provide a method for manufacturing mirrors that does not have these drawbacks.
本発明に従えば、透明ガラスシートの裏面に反射層を適
用し、この反射層の上に1層あるいは数層の保護層を被
覆することからなり、該保護層がシートの被覆裏面化電
子ビーム硬化性樹脂組成物の被覆を適用し、樹脂を一つ
あるいはいくつかの電子ビーム中で硬化させ密着保護層
を形成せしめることを特徴−とする鏡の製造法が提供せ
られる。According to the invention, a reflective layer is applied to the back side of a transparent glass sheet, and one or several protective layers are coated on top of this reflective layer, said protective layer being applied to the backside of the sheet by electron beams. A method of manufacturing a mirror is provided, characterized in that a coating of a curable resin composition is applied and the resin is cured in one or several electron beams to form an adhesive protective layer.
本発明を利用することにより、樹脂層は数秒で硬化せし
められ、従って、新しく製造された鏡を湿潤保護層が結
着しないよう注意をはらう必要なしに所望により積み重
ねることができ連続的な生産を容易に実施することがで
きる。また溶媒蒸発の問題も実質的に回避しつる。By utilizing the present invention, the resin layer is cured in seconds, and thus newly manufactured mirrors can be stacked as desired without the need to take care to prevent wet protective layers from clumping together, allowing for continuous production. It can be easily implemented. The problem of solvent evaporation is also substantially avoided.
また電子ビーム硬化は光放射線による硬化法に比し大き
な利点がある。まず、樹脂組成物中に光開始剤を加える
必要がない。11!2に樹脂層が光放射線を透過せしめ
る必要性はないので、任意の所望顔料あるいは充填剤を
樹脂に加えることができ、また樹脂層を厚くすることが
できるので反射層に対する良好な保護を与えることがで
きる。Furthermore, electron beam curing has significant advantages over curing methods using optical radiation. First, there is no need to add a photoinitiator into the resin composition. 11!2 Since there is no need for the resin layer to be transparent to optical radiation, any desired pigments or fillers can be added to the resin, and the resin layer can be made thicker to provide good protection for the reflective layer. can give.
事実ガラスシートに何らかの理由で適用される樹脂組成
物を電子ビームで硬化させることには望ましくないとす
る偏見があった。これは、ガラスシートに電子ビームを
照射すると光学特性番こ悪影響があるということが理論
的6〔推論されていたからである。しかしながら今回こ
の予想された悪影響はさほど大ではなく、鏡の緒特性に
およぼす劣化も許容限度内であることが見出された。従
って、上述の種々の利点をそなえた電子ビーム硬化を利
用することができる。In fact, there has been a prejudice that it is undesirable to cure resin compositions applied to glass sheets with electron beams for any reason. This is because it has been theoretically inferred that irradiating a glass sheet with an electron beam will have an adverse effect on its optical properties. However, this time it was found that the expected adverse effect was not so great, and the deterioration in the mirror properties was within tolerable limits. Therefore, electron beam curing can be utilized with the various advantages mentioned above.
前記電子ビーム硬化は例えは窒素雰囲気の如く不活性大
気中で実施せねばならぬ。というのはこの段階で酸素が
存在すると形成される保護被償の質に悪影響がある。実
質的に不活性の大気は連続操作においても、例えば大気
圧以上で不活性ガスを連続的に供給するトンネル室内で
硬化を行なわしめることにより、極めて容易に保つこと
ができる。不活性ガスとして窒素を用いるのが経済的で
好都合であるため好ましい。The electron beam curing must be carried out in an inert atmosphere, such as a nitrogen atmosphere. The presence of oxygen at this stage has a negative effect on the quality of the protective cover formed. A substantially inert atmosphere can be maintained very easily even in continuous operation, for example by carrying out the curing in a tunnel chamber with a continuous supply of inert gas at or above atmospheric pressure. It is preferred to use nitrogen as the inert gas because it is economical and convenient.
使用せられる樹脂組成物は好ましくは重fr%で下記か
らなる。The resin composition used preferably consists of the following in weight fr%:
可塑剤 θ〜40%顔料および
/または充填材 0〜40%゛他の添加剤
0.5〜10%電子ビーム
はこのベース材料(作用し連鎖延長および/または交叉
結合反応により迅速な硬化を達成せしめる。適当なオリ
ゴマーの例は下記タイプのものである:ポリウレタンア
クリレート、エポキシアクリレート、ポリエステル−ポ
リオールアクリレート、ポリエーテル−ポリオールアク
リレートおよびポリエン−ポリチオール。Plasticizer θ~40% Pigment and/or filler 0~40% Other additives 0.5~10% The electron beam acts on this base material to achieve rapid curing through chain extension and/or cross-linking reactions. Examples of suitable oligomers are of the following types: polyurethane acrylates, epoxy acrylates, polyester-polyol acrylates, polyether-polyol acrylates and polyene-polythiols.
反応性稀釈剤は、例えはベース材料の粘度を低下させる
ために用いられる。特にポリウレタンおよびエポキシア
クリレートベース材料の粘度を低下させるには単官能あ
るいは多官能アクリレートが用いられる。反応性稀釈剤
はベース材料を電子ビームで賦活する時にベース材料と
混合せられる。Reactive diluents are used, for example, to reduce the viscosity of the base material. In particular, mono- or polyfunctional acrylates are used to reduce the viscosity of polyurethane and epoxy acrylate-based materials. The reactive diluent is mixed with the base material when the base material is activated with an electron beam.
可塑剤、顔料、充填材および塗料製造に通常使用せられ
るその他の添加剤も所望により使用せられる。Plasticizers, pigments, fillers and other additives commonly used in paint manufacture are also optionally used.
有利には、前記硬化はシートの樹脂被覆面をカーテン状
の電子ビーム(群)でひとけきすることにより実施せら
れる。これは硬化のための簡単かつ好都合な方法である
。Advantageously, said curing is carried out by stroking the resin-coated side of the sheet with a curtain-like electron beam(s). This is a simple and convenient method for curing.
好ましくは、前記の放射線硬化性樹脂被覆がカーテン塗
布法により適用せられる。かかる方法は高品質の均一な
厚みの薄い被覆を作るのに有利である。Preferably, the radiation curable resin coating described above is applied by curtain coating. Such a method is advantageous in producing thin coatings of high quality and uniform thickness.
該樹脂被覆は厚みが少なくとも20μm、好ましくは3
0〜80μmの密着保護層を与えるように適用され、硬
化せしめられるのが有利である。The resin coating has a thickness of at least 20 μm, preferably 3 μm.
Advantageously, it is applied and cured to provide an adherent protective layer of 0 to 80 μm.
上記最少限の厚みの被覆が反射層に対し優れた保護を与
え、前記の好ましい範囲の厚みが硬化の容易性ならびに
樹脂の経済的な使用を保証する。A coating of the above minimum thickness provides excellent protection for the reflective layer, and a thickness in the above preferred range ensures ease of curing and economical use of the resin.
前記硬化のため樹脂組成物は3〜Ionラドを吸収せし
められることが好ましい。かかる量が有効力1つ迅速な
硬化に寄与する。For said curing, the resin composition is preferably allowed to absorb 3-Ion rad. Such an amount contributes to rapid curing by one effective force.
本発明は多数の鏡が樹脂被覆ステーションと硬化ステー
ション中を連続的番こ運搬せられる鏡の連続ライン生産
番と特化好ましく適用せられる。The present invention has particular application in continuous line production of mirrors in which a large number of mirrors are transported successively through resin coating and curing stations.
本発明は本願明細書記載の方法で製造された鏡を包含し
、またかかる方法化用いられる中間体製品にまでおよぶ
ものである。The present invention includes mirrors made by the methods described herein, and also extends to intermediate products used in such methods.
従って、本発明はまた本発明方法で鏡を製造するのに用
いられる中間体製品で透明ガラスシートの裏面に反射層
がもうけられ、密着保護層を得るのに硬化せしめられる
電子ビーム硬化性樹脂組成物の表面被覆を有するものが
提供せられる。Therefore, the present invention also provides an electron beam curable resin composition, which is an intermediate product used for manufacturing mirrors according to the method of the present invention, in which a reflective layer is provided on the back side of a transparent glass sheet, and which is cured to obtain an adhesive protective layer. A surface coating of an object is provided.
以丁添付図により本発明の好ましい具体例を説明する。Preferred embodiments of the present invention will now be described with reference to the accompanying drawings.
第1図は透明ガラスシート1の裏面(上面)に反射層2
を有し、その上に中間層3と電子ビーム硬化樹脂被覆か
ら作られた保護層4を有するものからなる鏡を示す。Figure 1 shows a reflective layer 2 on the back (top) of a transparent glass sheet 1.
1 and having thereon an intermediate layer 3 and a protective layer 4 made of an electron beam cured resin coating.
例えは銀の反射層2と銅の中間層3は既知方法で適用せ
られる。中間層3の主目的は反射層2の酸化を防止する
ことにある。本発明は保護層4を適用する点に特徴があ
る。For example, the reflective layer 2 of silver and the intermediate layer 3 of copper are applied in known manner. The main purpose of the intermediate layer 3 is to prevent the reflective layer 2 from oxidizing. The present invention is characterized in that a protective layer 4 is applied.
密着保護層4を適用する装置が第2図に示されている。An apparatus for applying the adhesive protective layer 4 is shown in FIG.
第2図において反射被覆(図示なし)と任意的中間被覆
(図示なし)を有する透明ガラスシート5はコンベア6
により被覆装置7、好適にはカーテン被覆装置の下を通
過せしめられそこで電子ビーム硬化性樹脂の被覆8が適
用せられる。コンベア6はこのように被覆されたシート
群ヲトンネル室9中に運びそこでカーテンタイプ電子プ
ロセッサ11により発生せしめられる電子ビームlOに
より前記被WI8が処理される。トンネル室9はタンク
12からの不活性ガス例えば窒素ガスによりフラッシュ
される・トンネルの入口13は被覆シート5との間に空
間を残し出来るだけ低くなっており、トンネル出口14
はタンク12からのガスの消費を少なくし、トンネル室
9内に実質的に不活性雰囲気を容易に保持するため図示
せる如く可撓性カーテン15.により密閉されていても
かまわない。In FIG. 2, a transparent glass sheet 5 with a reflective coating (not shown) and an optional intermediate coating (not shown) is conveyed to a conveyor 6.
is passed under a coating device 7, preferably a curtain coating device, where a coating 8 of electron beam curable resin is applied. The conveyor 6 transports the thus coated sheets into a tunnel chamber 9 where the WI 8 is treated with an electron beam IO generated by a curtain-type electronic processor 11. The tunnel chamber 9 is flushed with an inert gas, for example nitrogen gas, from a tank 12.The tunnel entrance 13 is as low as possible leaving a space between it and the covering sheet 5, and the tunnel exit 14
In order to reduce the consumption of gas from the tank 12 and to facilitate maintaining a substantially inert atmosphere within the tunnel chamber 9, a flexible curtain 15. is provided as shown. It does not matter if it is sealed.
ある特定例化おいて、鏡−被覆ガラスシート5は2.0
m 7分の速度で運搬されなからカーテン被覆法番こ
より電子ビーム硬化性樹脂被覆が、適用される。In one particular embodiment, the mirror-coated glass sheet 5 has a diameter of 2.0
From the curtain coating method, an electron beam curable resin coating is applied, conveyed at a speed of 7 minutes.
各々の電子ビーム加速装置がシート幅1.7mを受けも
ち、幅3.4mのシートを処理するため二つの加速装置
が端と端を接してもうけられる。Each electron beam accelerator serves a sheet width of 1.7 m, and two accelerators are provided end-to-end to process a 3.4 m wide sheet.
これら加速装置はジエネバのイー・ニス・アイから市販
されている1 75 KaVアクセレーターであったが
、l 5 Q KaVアクセレーターも用いることがで
きた。These accelerators were 175 KaV accelerators available from E.N.I. of Zieneva, but l5Q KaV accelerators could also be used.
樹脂被覆は勿論使用される樹脂組成物によりことなるが
、約120 t/lelに相当する厚み60μmに適用
された。樹脂被覆により吸収された量は6mラド(6X
IC1−IIGy)であった。The resin coating was applied to a thickness of 60 μm, which corresponds to about 120 t/l, although it of course varies depending on the resin composition used. The amount absorbed by the resin coating is 6 mrad (6X
IC1-IIGy).
使用せられる樹脂組成物は下記一般的組成を有する(重
量%)。The resin composition used has the following general composition (% by weight):
不飽和モノマーあるいはオリゴマーを
含む電子ビーム硬化性ベース材料 10〜90%
可塑剤 0〜40%顔料および
/または充填材 0〜40%他の添加剤
0.5〜1〇−以下実施例に
より本発明を説明する。Electron beam curable base material containing unsaturated monomers or oligomers 10-90%
Plasticizer 0-40% Pigments and/or fillers 0-40% Other additives
0.5 to 10 - The present invention will be explained below with reference to Examples.
実施例 1
プレックス662B−0(o−ム社) 60重i
t%酸化鉛 7
酸化チタン 7炭酸カルシウ
ム i。Example 1 Plex 662B-0 (OM Co., Ltd.) 60 weight i
t% Lead oxide 7 Titanium oxide 7 Calcium carbonate i.
実施例 2
電子ビーム硬化性ベース材料として、
ジエチレングリコールジアクリレート°15ジオクチル
フタレート 2 。Example 2 Diethylene glycol diacrylate 15 dioctyl phthalate 2 as electron beam curable base material.
酸化鉛 7炭酸カルシウ
ム 1゜硫酸バリウム
1゜実施例 3
テトラエチレングリコールジアクリレ
ート 1
5酸化鉛 5
炭酸カルシウム 7炭酸マグネシ
ウム 15酸化鉄
4
このように保護された鏡の光反射率およびエネルギー反
射特性は電子ビーム照射で硬化された保i11層のない
類似の鏡のものと実質的に同じである。Lead oxide 7 Calcium carbonate 1° Barium sulfate
1゜Example 3 Tetraethylene glycol diacrylate 1
5 Lead oxide 5 Calcium carbonate 7 Magnesium carbonate 15 Iron oxide
4 The light reflectance and energy reflection properties of a mirror thus protected are substantially the same as those of a similar mirror without the protective i11 layer cured by electron beam irradiation.
第1図は本発明方法で製造せられる鏡の断面図、第2図
は本発明方法の実・胞化用いられる装置の1部分の略図
的断面図。
特許出願人 グラヴルベル
ν号1
手続補正寄生
硫
3、補正をする者
事件との関係 1「ν[叙摘メ;
ボ社禰妊卦l乳
低二門V称 ’7”> 5’+レヘ“亀し′4、代
理人FIG. 1 is a cross-sectional view of a mirror manufactured by the method of the present invention, and FIG. 2 is a schematic cross-sectional view of a portion of the apparatus used in the method of the present invention. Patent applicant Gravel Bell ν No. 1 Procedural amendment parasitic sulfur 3, relationship with the case of the person making the amendment 1 "ν shi'4, agent
Claims (1)
層を1層あるいは多層の保護層で力、4−することから
なり、前記保護層あるいはその1層がガラスシートの被
覆裏面に電子ビーム硬化性樹脂組成物を適用し電子ビー
ム(、群)中で該樹脂を硬化させ密着保護層とすること
により形成せられることを特徴とする鏡の製造方法。 2、樹脂組成物が重量で 可塑剤 0〜40%顔料およ
び/または充填剤 0〜40%その他の
添加剤(群)0.5〜10% からなる特許請求の範囲第1項記載の方法。 3、前記の硬化がシートの樹脂被覆面をカーテン状の電
子ビーム(群)による押流しにより実施せられる特許請
求の範囲第1項あるいは第2項記載の方法。 4、放射線硬化形樹脂被覆がカーテンコーティング法に
より適用せられる特許請求の範囲第1項〜第3項のいず
れかに記載の方法。 5、前記の樹脂被覆が、厚み少なくとも20μm、好ま
しくは30〜80′μmの密着保護層を残存せしめるよ
うに適用され硬化せしめられる特許請求の範囲第1項〜
第4項のいずれかに記載の方法。 6、樹脂組成物が硬化のため3〜10字ラドの電子ビー
ムを吸収せしめられる特許請求の範囲第1項〜第5項の
いずれかに記載の方法。 7、多数の鏡群が連続的に樹脂被覆ステーションと硬化
ステーション中を通過するよう運搬される特許請求の範
囲第1項〜第6項のいずれかに記載の方法。 8、実質的に本願明細書に記載された特許請求の範囲の
いずれか番こかかる鏡の製造法。 9、特許請求の範囲のいずれかに記載の方法で製造され
た鏡。 10、透明ガラスシートの裏面に反射層と、密着保護層
を作るため硬化可能な電子ビーム硬化型樹脂組成物の表
面被覆を有する特許請求の範囲第1項〜第8項のいずれ
かに記載の方法による鏡の製造に用いられる中間体製品
。[Claims] 1. A reflective layer is applied to the back surface of a transparent glass sheet, and the reflective layer is covered with one or more protective layers, and the protective layer or one layer is made of glass. 1. A method for manufacturing a mirror, comprising applying an electron beam curable resin composition to the coated back side of a sheet and curing the resin in an electron beam (or groups) to form an adhesive protective layer. 2. The method according to claim 1, wherein the resin composition comprises, by weight, 0 to 40% plasticizer, 0 to 40% pigment and/or filler, and 0.5 to 10% other additive(s). 3. The method according to claim 1 or 2, wherein the curing is carried out by sweeping the resin-coated surface of the sheet with a curtain-like electron beam (group). 4. The method according to any one of claims 1 to 3, wherein the radiation-curable resin coating is applied by a curtain coating method. 5. The resin coating is applied and cured in such a way as to leave an adhesive protective layer with a thickness of at least 20 μm, preferably between 30 and 80′ μm.
The method according to any of paragraph 4. 6. The method according to any one of claims 1 to 5, wherein the resin composition is made to absorb an electron beam of 3 to 10 rad for curing. 7. A method according to any one of claims 1 to 6, in which a number of mirror groups are conveyed successively through a resin coating station and a curing station. 8. A method of manufacturing a mirror according to substantially any of the claims herein. 9. A mirror manufactured by the method according to any of the claims. 10. The transparent glass sheet according to any one of claims 1 to 8, which has a reflective layer on the back surface and a surface coating of a curable electron beam curable resin composition to form an adhesion protective layer. Intermediate products used in the manufacture of mirrors by process.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8236343 | 1982-12-21 | ||
GB08236343A GB2132507B (en) | 1982-12-21 | 1982-12-21 | Mirrors |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59174546A true JPS59174546A (en) | 1984-10-03 |
Family
ID=10535138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58238727A Pending JPS59174546A (en) | 1982-12-21 | 1983-12-16 | Mirror |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS59174546A (en) |
BE (1) | BE898481A (en) |
DE (1) | DE3346048C2 (en) |
ES (1) | ES528669A0 (en) |
FR (1) | FR2537969B1 (en) |
GB (1) | GB2132507B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63170246A (en) * | 1986-12-22 | 1988-07-14 | ピーピージー・インダストリーズ・インコーポレイテッド | Mirror painting method |
JPH01301535A (en) * | 1988-05-31 | 1989-12-05 | Hayakawa Rubber Co Ltd | Protective film material for glass or mirror |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4904265A (en) * | 1988-09-09 | 1990-02-27 | Boehringer Mannheim Corporation | Cementless acetabular implant |
GB8901684D0 (en) * | 1989-01-26 | 1989-03-15 | Glaverbel | Mirrors |
DE4022745A1 (en) * | 1990-07-18 | 1992-01-23 | Hans Lang Gmbh & Co Kg Ing | Mirror patterning - uses laser beam directed through glass pane to evaporate the reflection layer partially |
FR2843384A1 (en) * | 2002-08-09 | 2004-02-13 | Saint Gobain | Polymer-coated safety glass is cut to size after application of liquid polymer but before its molecular mass is increased |
FR2967242B1 (en) | 2010-11-04 | 2014-11-07 | Cray Valley Sa | SOLAR REFLECTOR OF COMPOSITE MATERIAL BASED ON FIBER REINFORCED RESIN AND USES IN SOLAR POWER PLANTS |
FR2971960B1 (en) * | 2011-02-25 | 2013-02-22 | Saint Gobain | THERMAL COATING TREATMENT WITH LASER |
DE102015005584A1 (en) * | 2015-05-04 | 2016-11-10 | CRlSTALlCA GmbH | Process for coating glass surfaces |
FR3075784B1 (en) * | 2017-12-21 | 2019-12-20 | Saint-Gobain Glass France | MIRROR |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4942897A (en) * | 1972-09-02 | 1974-04-22 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL154236B (en) * | 1971-02-10 | 1977-08-15 | Showa Highpolymer | PROCESS FOR PREPARING AN UNSATURATED EPOXYESTER RESIN, AND FORMED PRODUCTION, PROVIDED WITH A COATING LAYER OF SUCH EPOXYESTER RESIN. |
JPS5323851B2 (en) * | 1973-02-15 | 1978-07-17 | ||
US4039722A (en) * | 1974-01-08 | 1977-08-02 | Ford Motor Company | Plural coated article and process for making same |
US4255214A (en) * | 1977-11-21 | 1981-03-10 | Falconer Plate Glass Corporation | Methods of manufacturing and protecting mirrors |
-
1982
- 1982-12-21 GB GB08236343A patent/GB2132507B/en not_active Expired
-
1983
- 1983-12-16 JP JP58238727A patent/JPS59174546A/en active Pending
- 1983-12-16 BE BE1/10920A patent/BE898481A/en not_active IP Right Cessation
- 1983-12-19 FR FR838320435A patent/FR2537969B1/en not_active Expired - Lifetime
- 1983-12-20 DE DE3346048A patent/DE3346048C2/en not_active Expired - Fee Related
- 1983-12-21 ES ES528669A patent/ES528669A0/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4942897A (en) * | 1972-09-02 | 1974-04-22 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63170246A (en) * | 1986-12-22 | 1988-07-14 | ピーピージー・インダストリーズ・インコーポレイテッド | Mirror painting method |
JPH01301535A (en) * | 1988-05-31 | 1989-12-05 | Hayakawa Rubber Co Ltd | Protective film material for glass or mirror |
Also Published As
Publication number | Publication date |
---|---|
DE3346048C2 (en) | 1995-03-16 |
GB2132507B (en) | 1986-01-29 |
BE898481A (en) | 1984-06-18 |
DE3346048A1 (en) | 1984-06-28 |
FR2537969A1 (en) | 1984-06-22 |
GB2132507A (en) | 1984-07-11 |
FR2537969B1 (en) | 1992-01-10 |
ES8505320A1 (en) | 1985-05-16 |
ES528669A0 (en) | 1985-05-16 |
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