JPS61118236A - Molding method of non-glare sheet - Google Patents

Molding method of non-glare sheet

Info

Publication number
JPS61118236A
JPS61118236A JP59238544A JP23854484A JPS61118236A JP S61118236 A JPS61118236 A JP S61118236A JP 59238544 A JP59238544 A JP 59238544A JP 23854484 A JP23854484 A JP 23854484A JP S61118236 A JPS61118236 A JP S61118236A
Authority
JP
Japan
Prior art keywords
sheet
synthetic resin
resin sheet
glare
fine powder
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
Application number
JP59238544A
Other languages
Japanese (ja)
Inventor
Hiroshi Kataoka
片岡 紘
Kaoru Toyouchi
薫 豊内
Hiroshi Kuriaki
廣 栗秋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
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 by Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP59238544A priority Critical patent/JPS61118236A/en
Publication of JPS61118236A publication Critical patent/JPS61118236A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29DPRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
    • B29D7/00Producing flat articles, e.g. films or sheets
    • B29D7/01Films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion 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
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0018Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular optical properties, e.g. fluorescent or phosphorescent
    • B29K2995/0026Transparent

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Optical Elements Other Than Lenses (AREA)

Abstract

PURPOSE:To enable economic molding of a non-glare sheet having fine unevenness on the surface of the same, by a method wherein a synthetic resin sheet obtained by compounding a constant quantity of dust-size particles having an average particle diameter falling within a specific range is laminated, compressed by heating the same at a specific temperature and peeled off after cooling. CONSTITUTION:A smooth surfacelike non-crystalline transparent synthetic resin sheet 2 plasticized through heating and extruded from an extruding machine 1 contains 20-60wt% dust-size particles whose average particle diameter is 0.1mum-10mum. Both sides of the sheet 2 are put between sheets 3 molded beforehand and made into a three-tiered layer, which is cooled while it is being compressed by a roll 11. A fine uneven surface of the synthetic resin sheet 3 containing dust-size particle solids is transferred to the surface of the non- crystalline transparent synthetic resin sheet through compression by the roll 11. After the sheet has been cooled and cured, the resin sheet 3 containing the dust-size particles is rolled up by peeling the three-tiered layer and a non- glare sheet 4 is obtained.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、視覚表示端末等に使用される非結晶性透明合
成樹脂からなるノングレアシートの成形法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for molding a non-glare sheet made of amorphous transparent synthetic resin used for visual display terminals and the like.

(従来の技術) 透明合成樹脂シートの表面に一足範囲の微細な凹凸tつ
げて反射光を散乱させるいわゆるノングレアシートは、
最近各種視覚表示端末のカバーとして広く使用されるよ
5になった。このノングレアシートは、従来、透明合成
樹脂シートの表面に微粉末固体を吹きつげ℃シート表面
に凹凸をつけるいわゆるサンドブラスト法、透明合成値
脂シートにエンざスロールを押しつげる万伝、倣細な凹
凸を有するガラス板をセルとして用いたアクリル樹脂の
セルキャスト重合法、透明合成樹脂シート表面に透明塗
料を表面凹凸に塗布する方法等により成形されている。
(Prior art) A so-called non-glare sheet is a transparent synthetic resin sheet with minute irregularities on the surface to scatter reflected light.
Recently, it has become widely used as covers for various visual display terminals5. Conventionally, this non-glare sheet has been produced using the so-called sandblasting method, which involves blowing finely powdered solid onto the surface of a transparent synthetic resin sheet to create unevenness on the surface of the sheet. It is formed by a cell-cast polymerization method of acrylic resin using a glass plate having the same structure as a cell, or by a method of applying a transparent paint to the surface of a transparent synthetic resin sheet to form irregularities on the surface.

(発明が解決しよ5とする問題点) 上記従来の方床にはそれぞれ欠点が6す、品質あるいは
底形コストにおいて問題をか\えている。
(Problems to be Solved by the Invention) Each of the above-mentioned conventional square beds has drawbacks, such as problems in quality or bottom shape cost.

例えば、アクリル樹脂のセルキャスト重合法では、重合
されたアクリル樹脂シートが倣細な凹凸表面を有するガ
ラスと容易に#駿できず、ガラスが割れたり、樹脂シー
ト表面の一部がガラスの凹凸表面にはまり込んでとられ
たりする等の問題がある。
For example, in the cell-cast polymerization method of acrylic resin, the polymerized acrylic resin sheet cannot be easily bonded to glass that has a finely uneven surface, and the glass may break or a part of the resin sheet surface may be exposed to the uneven surface of the glass. There are problems such as it getting stuck and being removed.

(問題点を解決するための手段) 本発明者らは、上記の如き状況にあるノングレアシート
の製造方法について種々検討した結果、非結晶性透明合
成樹脂シートに特定範囲の平均粒径を有する微粉末の一
定tya−配合した合成樹脂シートが積層されかつ特足
温反に加熱された積層シートを圧縮し、冷却後該積層シ
ートを剥離することにより、上記問題点のないノングレ
アシートが得られることを見出し、本発811を完成し
た。。
(Means for Solving the Problems) As a result of various studies on manufacturing methods for non-glare sheets under the above-mentioned circumstances, the present inventors have found that a non-crystalline transparent synthetic resin sheet has fine particles having an average particle size within a specific range. A non-glare sheet free of the above problems can be obtained by compressing a laminated sheet in which synthetic resin sheets containing a certain amount of powder are laminated and heated to a particularly warm temperature, and then peeling off the laminated sheet after cooling. He discovered this and completed the original 811. .

即ち、本発明は、非結晶性透明合成樹脂シートに平均粒
径0.1〜10μmの微粉末v20〜60重tS含有す
る合成樹脂シートが積層され、かつ非結晶性透明合成樹
脂シートのガラス転位温度以上で該非Mn性透明−&f
y、樹脂シートの粘度か微粉末含有合am脂シートの粘
度より小さい状111に加熱されている8を鳩シートを
1シ一ト費面から圧細し、冷却後膣積層シートを剥離す
るノングレアシートのべりぬである。
That is, in the present invention, a synthetic resin sheet containing fine powder v20 to 60 weight tS with an average particle size of 0.1 to 10 μm is laminated to an amorphous transparent synthetic resin sheet, and the glass transition of the amorphous transparent synthetic resin sheet is Non-Mn transparent at temperatures above -&f
y, the viscosity of the resin sheet is smaller than the viscosity of the fine powder-containing synthetic resin sheet (8), which is heated to a state of 111. The pigeon sheet is compressed from the cost per sheet, and after cooling, the vaginal laminated sheet is peeled off. It's a slippery sheet.

特に、本発明は、特定範囲の平均粒径の微粉末を一定量
配合した合成樹脂シートの凹凸表面を、非結晶性透明(
lf脂シート弐面に該シートのめる粘度範囲で転写する
ことを特長とする。
In particular, the present invention aims to improve the uneven surface of a synthetic resin sheet containing a certain amount of fine powder with an average particle size within a specific range.
It is characterized by being able to transfer onto the second side of the lf oil sheet within a viscosity range that can be applied to the sheet.

本発明に用いる非結晶性透明合成樹脂シートは、透明、
あるいは牛透明な非結晶性合成樹脂であり、好ましくは
一般に硬質透明樹脂と云われ℃いるアクリル樹脂、ポリ
カーボネート有脂、ポリスチレン、スチレン−、アクリ
ロニトリル共重合体、硬質塩化ビニル等のシートでるる
。アクリル樹脂としてはメチルメタクリレ−ト(以後韮
ムと略称〕を生成分とする重合体であり、MU電合体(
以後PMMAと略称)、MMAを含有する共ム合体、P
MMAあるいはMMA #c、I[合体忙他ポリマーを
配合したポリマーブレンド等でるる。
The amorphous transparent synthetic resin sheet used in the present invention is transparent,
Alternatively, it is a transparent non-crystalline synthetic resin, preferably a sheet of acrylic resin, which is generally referred to as a hard transparent resin, polycarbonate with fat, polystyrene, styrene, acrylonitrile copolymer, hard vinyl chloride, or the like. The acrylic resin is a polymer containing methyl methacrylate (hereinafter abbreviated as nirum) as a product component, and MU electropolymer (
(hereinafter abbreviated as PMMA), MMA-containing conjugate, P
MMA or MMA #c, I [polymer blends containing other polymers are available.

MMA共東合体には凪とフルキルアクリレート共重合体
(以後Co(MMA−人ム)と略称)が良好に使用でき
る。アルキルアクリレートとしてメチルアクリレート、
エチルアクリレート、プロピルアクリレート、グチルア
クリレート、2−エチルへキシルアクリレート等の1〜
10it%共重合体が良好に使用できる。鹿ムー無水マ
レイン戚−スチレン3元系共重合体、MMA−メチルメ
タアクリルアミド共重合体等の耐熱アクリル樹脂も良好
に使用できる。この仙、MMAとスチレン、スチレン誘
導体、アクリロニトリル、メタクリロニトリル、アクリ
ル酸、メメクリル酸の1植あるいは2′M1以上の共重
合体が使用できる。ポリカーボネート樹脂としては、ビ
スフェノールAを含ひ芳香族ポリカーボネートである。
Nagi and furkyl acrylate copolymer (hereinafter abbreviated as Co (MMA-jinmu)) can be favorably used for the MMA co-topolymer. Methyl acrylate as alkyl acrylate,
1 to ethyl acrylate, propyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, etc.
A 10 it% copolymer can be used satisfactorily. Heat-resistant acrylic resins such as Shikamu anhydrous maleic-styrene ternary copolymer and MMA-methylmethacrylamide copolymer can also be used satisfactorily. Alternatively, a copolymer of MMA and styrene, a styrene derivative, acrylonitrile, methacrylonitrile, acrylic acid, or memethacrylic acid or a copolymer of 2'M1 or more can be used. The polycarbonate resin is an aromatic polycarbonate containing bisphenol A.

ポリスチレン、スチレン−7クリロニトリル共重合体、
硬質塩化ビニルとしては、一般に広(使用されている各
グレードがそのま一使用できる。谷倒脂には谷m添加g
iを配合することができる。染顔料、紫外線吸収剤、熱
線吸収剤、熱巌反射剤、熱安定剤、lJA燃剤、ガラス
繊維等を配合することができる。これ4!添加物により
シートの透明性あるいは透光性を太き(低下させないこ
とが好ましく、添加物及び各樹脂’kA宜選択して使用
することが好ましい。
Polystyrene, styrene-7crylonitrile copolymer,
Hard vinyl chloride is generally widely used (each grade used can be used as is.
i can be blended. Dyes and pigments, ultraviolet absorbers, heat ray absorbers, thermal reflectors, heat stabilizers, IJA fuel, glass fibers, etc. can be blended. This is 4! It is preferable that the transparency or translucency of the sheet is increased (not reduced) by the additive, and it is preferable to use the additive and each resin by selecting them as appropriate.

また、該非結晶性透明樹脂シートの厚さはシートの使用
目的に応じ各厚みのシートが使用できるが、好ましくは
0.05關〜20關、更に好ましくは0.1 yn、〜
10關のものが使用できる。
Further, the thickness of the amorphous transparent resin sheet may be different depending on the purpose of use of the sheet, but preferably 0.05 to 20 mm, more preferably 0.1 yn to 20 mm.
10 parts can be used.

本発明に用いる微粉末?配合した合成樹脂シートは、非
結晶性透明合成樹脂より軟化温度が高い樹脂が用いられ
、一般に結晶性樹脂が好ましく、ポリエチレン、ポリプ
ロピレン等のポリオレフ −(ン、ナイロン6、ナイロ
ン66、ナイロン12%のポリアミド、のシートが特に
好ましい。
Fine powder used in the present invention? For the compounded synthetic resin sheet, a resin having a higher softening temperature than an amorphous transparent synthetic resin is used, and crystalline resins are generally preferred. Particularly preferred are sheets of polyamide.

微粉7:配合合成樹脂シートは加熱圧縮した時に積層す
る非結晶性透明f−成衛樹脂−トと非接層性であること
が必要でるる。例えば、非結晶性透明合成樹脂シートと
してアクリル樹脂゛を使用した場合には、微粉未配合合
成側脂シートとじ又ポリオレフィン、ポリアミドのシー
トを1!2用すると、互に非接層性であり、良好に使用
できる。懺粉床配合樹脂シートの厚みは0.01騙〜5
ム程度が良好に使用でさ、更に好lしくは0.02麹〜
I IIKの厚みである。微粉未配合傭脂シートは圧縮
成形後剥離するため、剥離強度に耐えるだけの厚みが必
要であり、−万、厚丁ぎることは不経済である。本発明
で述べる「シート」とは0−Ll 1 m犀のシートも
含み、「シート及びフィルム」を意味する。
Fine Powder 7: The compounded synthetic resin sheet needs to be non-contactable with the amorphous transparent f-singing resin sheet that is laminated when it is heated and compressed. For example, when acrylic resin is used as the amorphous transparent synthetic resin sheet, if one or two sheets of polyolefin or polyamide are used together with a synthetic side fat sheet that does not contain fine powder, they will not be in contact with each other. Can be used in good condition. The thickness of the resin sheet mixed with powder bed is 0.01 ~ 5
It is best to use koji of 0.02 to 100 g.
I IIK thickness. Since a grease sheet not containing fine powder peels off after compression molding, it needs to be thick enough to withstand peel strength, and it is uneconomical to make it too thick. The "sheet" mentioned in the present invention includes a sheet of 0-Ll 1 m rhinoceros, and means "sheet and film".

微粉末配合樹脂シートに用いられる微粉末は、平均粒径
が0.1μm〜10′μmの微粉末固体で6つ、メルク
、炭酸カルシウム、硫酸バリウム、硫酸カルシウム、ワ
ラストナイト、長石、マイカ、カオリン、クレー等の微
粉末が使用できる。微粉末固体の粒径と添加量により、
成形さ4.る非結晶性透明樹脂シートの異面状態が異り
、ノングレア性が異って(る。好ましいノングレア性を
示す表面凹凸にするには、微粉末の平均粒径が0.1顯
〜10μm1合hJt衝脂に奈加する微粉末の添加室が
201重%〜60!1%の範囲でおる。粉末固体の粒径
が小さ丁ぎると、成形品が透明に近(なり、ノングレア
性が発憚できない。粉末固体の粒径が犬すすキると、ノ
ングレアにはなるが不透明になる。
The fine powders used in the fine powder blended resin sheet are six types of fine powder solids with an average particle size of 0.1 μm to 10' μm: Merck, calcium carbonate, barium sulfate, calcium sulfate, wollastonite, feldspar, mica, Fine powders such as kaolin and clay can be used. Depending on the particle size and amount of fine powder solid,
Molded 4. The non-glare properties of the non-crystalline transparent resin sheets are different, and the non-glare properties are different. In order to create a surface roughness exhibiting preferable non-glare properties, the average particle size of the fine powder is 0.1 to 10 μm. The amount of fine powder added to hJt fat is in the range of 201% to 60!1% by weight.If the particle size of the powder solid is too small, the molded product will become nearly transparent and the non-glare properties will not be maintained. If the particle size of the powder solid is small enough, it becomes non-glare but opaque.

平均粒径0.1 μm〜10 IML、添加t20〜6
0iL童チがノングレア性を示しつ\ミある程度のa稠
性を維持できるシートの成形に好ましく、爽に好ましく
は微粉末の平均粒径が0.3顯〜5μm1添加重が25
ムit%〜50m[11Jでめる0微粉末一体の添加量
が20*j11%以下では好ましい微細な凹凸光面が得
られず、60iji%以上は樹脂に練込むのが困難にな
る。
Average particle size 0.1 μm ~ 10 IML, addition t20 ~ 6
0iL powder is suitable for forming sheets that exhibit non-glare properties and can maintain a certain degree of consistency, and is preferably fine powder with an average particle size of 0.3 to 5 μm and an added weight of 25
If the amount of fine powder added is less than 20*j11%, a preferable finely uneven optical surface cannot be obtained, and if it is more than 60 iji%, it becomes difficult to knead into the resin.

本発明は微粉末含有の合成樹脂シートを、非結晶性合成
樹脂透明シートと積層し、非結晶性透明合成樹脂のガラ
ス転移温度以上で、且つ非結晶性透明合成樹脂の粘度が
微粉末含有合成樹脂の粘度より小さい状態で、積層シー
トをシート狭面から圧縮し、次いで両シートを剥離する
方法でめる。
In the present invention, a synthetic resin sheet containing fine powder is laminated with a transparent sheet of amorphous synthetic resin, and the viscosity of the amorphous transparent synthetic resin is higher than the glass transition temperature of the amorphous transparent synthetic resin, and the viscosity of the amorphous transparent synthetic resin is higher than that of the synthetic resin containing fine powder. The laminated sheet is compressed from the narrow side of the sheet at a viscosity lower than that of the resin, and then both sheets are peeled off.

両シートを接触させ圧縮する方法には、加熱ロールで圧
縮する方法、プレスで圧締する万′f&等かめる。圧縮
する時の温度は上記粘度関係の範囲で過度に選択される
が、平滑な非#d’&性*脂シート表面かノングレア表
面に変形できるだけの粘度でるる必要がある。圧締力が
大きい揚台にはこの範囲の中の高粘度状態で成形できる
。好ヱしい圧権力はシート当10〜500AcjF/a
m”、更に好ましくは60〜600耀/dでめり、この
圧力は樹脂の粘度、圧#ii時間等により過当に選択さ
れる。
Methods for bringing the two sheets into contact and compressing include compressing with heated rolls, compressing with a press, and the like. The temperature at the time of compression is selected excessively within the range of the above viscosity relationship, but the viscosity must be high enough to transform it into a smooth non-#d'&gold* sheet surface or a non-glare surface. Molding can be performed at a high viscosity within this range on a platform with a large clamping force. The preferred pressure force is 10 to 500 AcjF/a per sheet.
m'', more preferably 60 to 600 m/d, and this pressure is properly selected depending on the viscosity of the resin, pressure #ii time, etc.

本発明の爽に好ましい成形法は、圧縮成形でシート表面
のノングレア化とシートの姑伸ン同時に行う方法である
。非結晶性合成樹脂シートと微粉末配合樹脂シートの積
層体を、内弐面に潤滑剤が塗布された圧縮金型で、該積
層体有脂シートのガラス転移温度以上、溶融点温度以下
の状態で、圧縮して金型内でプラグフローさせ″C2軸
配向させ、冷却後[成形品を金型より収り出し、各層を
剥離して211IB配向されたノングレアシートが得ら
れる。
A particularly preferred molding method of the present invention is a method in which the sheet surface is made non-glare and the sheet is stretched at the same time by compression molding. A laminate of an amorphous synthetic resin sheet and a finely powdered resin sheet is placed in a compression mold whose inner surface is coated with lubricant at a temperature above the glass transition temperature and below the melting point temperature of the laminate fat sheet. The molded product is compressed and allowed to plug flow in the mold to achieve C2 axis orientation, and after cooling, the molded product is taken out of the mold and each layer is peeled off to obtain a 211IB oriented non-glare sheet.

非結晶性合成樹脂シートは必要に応じて、互に接着性の
2層以上のシートでも良い。屈折率の小さい透8A樹脂
を元の波長の叔分の1の厚さに検層したノングレアシー
トは元の反射を減少させる拗らぎがあり、更に好ましい
。屈折率の小さい透明樹脂としては、各檀フッ素樹脂が
良好に使用でざる。
The amorphous synthetic resin sheet may be a sheet of two or more mutually adhesive layers, if necessary. A non-glare sheet made of transparent 8A resin having a low refractive index and having a thickness that is one-tenth of the original wavelength is more preferable because it has a waviness that reduces the original reflection. As a transparent resin with a small refractive index, various fluororesins are suitable for use.

以下、図面により本発明を説明する。The present invention will be explained below with reference to the drawings.

第1図は、本発明を実施するM様のフロシートでるる。FIG. 1 shows a flow sheet for Mr. M who implements the present invention.

第1図に於て、押出機1より加熱可塑化されて押出され
た平滑表面状の非結晶性透明合成樹脂シート2は、平均
粒径が0.1μm〜10μmの微粉末ya−20重tチ
から60憲量%含有する合成樹脂から成る、あらかじめ
成形されたシート3で両側をはさまれて3層シートとな
り、ロール11で圧縮されながら冷却される。このロー
ル11による圧縮により、微粉末固体含有合成樹脂シー
ト3の微細な凹凸表面が非結晶性透明合成樹脂シート茨
司に転写される。シートが冷製同化された麦、6層シー
トを剥離して微粉宋言有樹脂シート3Y巻ざ取り、ノン
グレアシート4を得る。8g1図では非結晶性樹脂シー
ト2の両表面をノングレア化する揚台について示したが
、微粉末富有合[[脂シート3ン片表面だけに圧縮てれ
は片弐面ソングレアのシートが得られる。
In FIG. 1, a smooth-surfaced non-crystalline transparent synthetic resin sheet 2 heated and extruded from an extruder 1 is made of fine powder ya-20 weight tons with an average particle size of 0.1 μm to 10 μm. The three-layer sheet is sandwiched between two pre-formed sheets 3 made of synthetic resin containing 60% by weight of water, and is cooled while being compressed by rolls 11. By this compression by the roll 11, the finely uneven surface of the fine powder solid-containing synthetic resin sheet 3 is transferred to the amorphous transparent synthetic resin sheet Ibarashi. The sheet is cold assimilated, the 6-layer sheet is peeled off, and the finely powdered resin sheet 3Y is rolled up to obtain the non-glare sheet 4. Fig. 8g1 shows a lifting platform that makes both surfaces of the amorphous resin sheet 2 non-glare, but when the powder is enriched, a sheet with a single glare on one side can be obtained.

第2図は本発明を実施する他の態様の70シートである
FIG. 2 shows 70 sheets of another embodiment of the present invention.

第2図に於て、異面平滑な非結晶性合成樹脂透明シート
2と微粉末を含有する合成樹脂シート3を積層して3層
とし、加熱された圧kd蓋型12で非結晶性透明合成樹
脂のガラス転移温度以上で、且つ該透明合成樹脂シート
の粘度が′4R粉木含有衝脂シートの粘度より/J’s
さい吠急になる温度に加熱しつ\圧縮しく第2図ム)、
仄いで冷却した後微粉末含有合成樹脂シート3を剥離し
て非結晶性合成樹脂の両面ノングレアシート4を得る(
第2図B)。
In Fig. 2, a different smooth amorphous synthetic resin transparent sheet 2 and a synthetic resin sheet 3 containing fine powder are laminated to form three layers, and a heated pressure kd lid mold 12 is used to form an amorphous transparent sheet. The temperature is higher than the glass transition temperature of the synthetic resin, and the viscosity of the transparent synthetic resin sheet is '4R than the viscosity of the powdered wood-containing fat sheet /J's
Heat it to a temperature that increases rapidly and compress it (Fig. 2).
After cooling in the air, the fine powder-containing synthetic resin sheet 3 is peeled off to obtain a double-sided non-glare sheet 4 of amorphous synthetic resin (
Figure 2B).

第6図は、不発明を央Δゐする史に他の機嫌の70シー
トである。
Figure 6 shows 70 sheets of other moods in the history of non-invention.

第3図に於て、圧#翁型12の内表面13に欄撹剤を塗
布した後、4枚の狭面平滑な非結晶性透明曾成樹脂シー
ト2の各界面と表嶽面に該シートと非接層性の微粉末含
有合成樹脂シート3’i−置き、圧縮金型12内に置(
(第3図ム)。該積層体を非結晶性透明台g樹脂シート
2のガラス転移温良以上、溶融点以下でるり、且つ非結
晶性透明合成w脂シート2の粘度が*粉床貧有樹脂シー
ト3の粘度より小さくなる感度に加熱した後、圧動して
積層体tプラグ7a−させて2軸配向シート5′1に成
形しく第3図B)゛、そのま\冷却した後2@配同シー
ト5y!−圧縮戴型12より取り出しく第3図C)、次
いで各シートを剥離して、2軸配向されたノングレア表
面を有する4枚のシート5を得る(第3図D)。
In FIG. 3, after applying a column stirring agent to the inner surface 13 of the pressure mold 12, it is applied to each interface and surface of the four narrow-sided smooth non-crystalline transparent synthetic resin sheets 2. A synthetic resin sheet 3'i-containing fine powder that is not in contact with the sheet is placed and placed in a compression mold 12 (
(Figure 3). The laminate is heated so that the glass transition temperature of the amorphous transparent resin sheet 2 is higher than the melting point, and the viscosity of the amorphous transparent synthetic resin sheet 2 is lower than the viscosity of the powder bed resin sheet 3. After heating to a sensitivity of 2, the laminate 7a is pressed and formed into a biaxially oriented sheet 5'1 (Fig. 3B). - Remove from the compression mold 12 (FIG. 3C) and then peel off each sheet to obtain four sheets 5 with biaxially oriented non-glare surfaces (FIG. 3D).

第4図は、本発明を実施する更にまた他の態様の70シ
ートを示す。
FIG. 4 shows 70 sheets of yet another embodiment of the present invention.

第4図に於て、非結晶性透明樹脂シート2と、該非結晶
性透明樹脂シート2と接層性を有する樹脂シート7にラ
ミネートされたJilc橿衝脂シ有脂8のラミネートシ
ート9、両表面に微粉末含有合成樹脂シート304枚(
第4図ム)Y!ね合せて2細延伸する積層シートとし、
第6図に示したと同様忙、@滑剤13を内表面に塗布し
た圧縮金型12にはさんで加熱しく第4図B)、金型内
でプラグ7r:1−させて2軸配向し、冷却後金型12
より取り出して、2軸延伸された微粉末倉荷有脂シート
6を剥離すると、ノングレア表am’v有する2軸延伸
されたラミネートシート10が得られる。
In FIG. 4, an amorphous transparent resin sheet 2, a laminate sheet 9 of Jilc resinous resin 8 laminated on a resin sheet 7 having layering properties with the amorphous transparent resin sheet 2, and both 304 synthetic resin sheets containing fine powder on the surface (
Figure 4) Y! A laminated sheet is made by kneading it together and stretching it into two thin layers.
In the same manner as shown in FIG. 6, the lubricant 13 is applied to the inner surface of the compression mold 12 and heated. Mold 12 after cooling
When the biaxially stretched fine powder warehouse fat sheet 6 is peeled off, a biaxially stretched laminate sheet 10 having a non-glare surface am'v is obtained.

(発明の効果) シートff面に微細な凹凸を有するノングレアシートを
経済的に成形することか従来困難でめったが、本発明に
より良好に成形できる様になった。
(Effects of the Invention) Conventionally, it has been difficult to economically form a non-glare sheet having minute irregularities on the sheet ff surface, but it has become possible to form it satisfactorily with the present invention.

核ノングレアシートは、ブラウン管等の視覚表示端末の
カバー、事務器、家庭電化製品等の銘板、各種計器のカ
バー等に良好に使用できる。
The nuclear non-glare sheet can be well used as covers for visual display terminals such as cathode ray tubes, nameplates for office equipment, home appliances, etc., covers for various instruments, etc.

実施例 第6図に示した方法によりノングレアシートを成形した
。次の谷賛脂シートを用いた。
Example A non-glare sheet was molded by the method shown in FIG. The following Tanishin fat sheet was used.

微粉末富有合成樹脂として第1表の組成を有する約0.
3關厚シートを用いた。
Approximately 0.0% fine powder rich synthetic resin having the composition shown in Table 1.
A 3-thick sheet was used.

(以下余白) 第  1  異 PP:ポリプロピレンポモボリマー HD−Pg :高密度ポリエチレン LD−PE :低密度ポリエチレン 非結晶性合成樹脂として第2衆の谷惇I脂を用いた。(Margin below) Part 1: Different PP: Polypropylene pomobolimer HD-Pg: High density polyethylene LD-PE: Low density polyethylene As the non-crystalline synthetic resin, Tanijun I fat from the second group was used.

W、2   表 使用した各樹脂の温度と粘度力関係を第5図〜纂7図に
示した。粘度はRheometrics工nc、aのD
ynamic Spectrometer RDS −
7700’t’用いて、シアーレイトω=1ラジアン/
抄と021027777秒で測定した。
W, 2 Table The relationship between temperature and viscosity of each resin used is shown in Figures 5 to 7. Viscosity is D of Rheometrics engineering nc, a.
dynamic Spectrometer RDS-
Using 7700't', shear rate ω=1 radian/
It was measured at 021027777 seconds.

圧縮金型12の内表面13に潤滑剤を塗布した後、4枚
の非結晶性合成樹脂シート原板の各界面と@裏面に酊5
枚の微粉末言臀曾成有脂シートを積層し、該&屠体を0
.1mm厚のPPシートで真空包装した後、下記の各温
度で圧縮して2軸配向成形した。
After applying lubricant to the inner surface 13 of the compression mold 12, lubricant 5 is applied to each interface and @back surface of the four amorphous synthetic resin sheet original plates.
Laminate sheets of finely powdered fat sheets and remove the carcass from
.. After vacuum packaging with a 1 mm thick PP sheet, it was compressed and biaxially oriented at the following temperatures.

PMMA        150℃ Co(MMA−AA)     130℃MMA−MM
Ami4    180 ’CMMA−BT−MAR1
80−C 圧動金型内で冷却固化した後、成形品を取り出し、各層
を剥離することによ−リ、非結晶性台成樹力dの2軸配
向シートを4枚得た。結果を第6表に示したO 本発明の条件範囲でのみ良好なノングレアシートが得ら
れた。
PMMA 150℃ Co(MMA-AA) 130℃MMA-MM
Ami4 180'CMMA-BT-MAR1
After cooling and solidifying in a 80-C pressure mold, the molded product was taken out and each layer was peeled off to obtain four biaxially oriented sheets with an amorphous stand formation force d. The results are shown in Table 6. Good non-glare sheets were obtained only within the condition range of the present invention.

(以下余白)(Margin below)

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

第1図は、本発明の1実施態様の70シート、第2図は
、本発明の他の実施態様の70シート、第6図は、本発
明の更に他の*施s徐の70シート、第4図は、不−A
明の更にまた他の実施態様のフロシートであり、褐5〜
7図は、実施例に使用した各樹脂の温度と粘度の関係を
示すグラフである。図中;1は押出機−12は非結晶性
透明台W、樹脂シート、3は微粉末含有合成樹脂シート
、4はノングレアシー1.5は2細配向ノングレアシー
ト、6は2軸配回された倣紛宋富有合或便脂シート、7
は非結晶性透明樹脂シート2と接層性を傅する衝力ぼシ
ート、8昏工樹刀「シート7に接7fされた異種樹脂シ
ート、9は樹脂シート7に異種樹脂シート8をラミネー
トしたシート、10は2軸延1甲されたラミネートシー
ト、11はロール、12は圧縮金型、13は圧縮金型1
2の内表面を示す。 特許出願人 旭化成工菓休式会社 第1図 第2図 (A)        (B) 第3図 第5図 (uu z Irad、/ sec、)+30  14
0  150  160  170  180遁庵(’
C) 第6図 130  140  150  160  170  
 旧0第7図 (uu * I rod、/富、) +50  160  170  180  190  
200  210温度(0C) 手続補正書(自発) 昭和60年2月−3日 特許庁長官   宇 賀 道 部 殿 1、事件の表示 昭和59年特許願第238544号 2、発明の名称 ノングレアシートの成形法 3、補正をする者 事件との関係  特許出願人 大阪府大阪市北区堂島浜1丁目2番6号4、補正の対象 明細書の「発明の詳細な説明」の欄 補正の内容 (1)、明細書第5頁第5行「使用できる。」の次に次
文を追加する。 「アクリル樹脂のブレンドとしては、Co (MMA−
AA)とポリフッ化ビニリデンのブレンド等が良好に使
用できる。」 (2)、同第7頁第5行「クレー等の微粉末が使用でき
る。」を「クレー、ガラスピーズ、ガラスバルーン、シ
ラスバルーン等の微粉末が使用できる。」と訂正する。 以上
FIG. 1 shows 70 sheets of one embodiment of the invention, FIG. 2 shows 70 sheets of another embodiment of the invention, and FIG. 6 shows 70 sheets of yet another embodiment of the invention. Figure 4 shows non-A
It is a flow sheet of still another embodiment of light, and brown 5 to
FIG. 7 is a graph showing the relationship between temperature and viscosity of each resin used in Examples. In the figure: 1 is an extruder, 12 is an amorphous transparent table W, a resin sheet, 3 is a synthetic resin sheet containing fine powder, 4 is a non-glare sheet 1.5 is a 2-fine oriented non-glare sheet, 6 is a biaxially arranged Imitation Song Dynasty wealth sheet or toilet fat sheet, 7
8 is a sheet of different resin that is in contact with sheet 7, and 9 is a sheet in which resin sheet 7 is laminated with a different resin sheet 8. , 10 is a biaxially stretched laminate sheet, 11 is a roll, 12 is a compression mold, 13 is a compression mold 1
The inner surface of 2 is shown. Patent Applicant: Asahi Kasei Koka Kaisha Ltd. Figure 1 Figure 2 (A) (B) Figure 3 Figure 5 (uu z Irad, / sec,) +30 14
0 150 160 170 180 Ton-an ('
C) Figure 6 130 140 150 160 170
Old 0 Figure 7 (uu * I rod, / wealth,) +50 160 170 180 190
200 210 Temperature (0C) Procedural amendment (voluntary) February-3, 1985 Michibe Uga, Commissioner of the Patent Office 1, Indication of the case 1982 Patent Application No. 238544 2, Name of the invention Molding of non-glare sheet Law 3, Relationship with the case of the person making the amendment Patent applicant 1-2-6-4 Dojimahama, Kita-ku, Osaka-shi, Osaka Prefecture Contents of the amendment in the "Detailed Description of the Invention" column of the specification to be amended (1) , the following sentence is added next to "Can be used." on page 5, line 5 of the specification. “As a blend of acrylic resin, Co (MMA-
Blends of AA) and polyvinylidene fluoride can be used satisfactorily. (2), page 7, line 5, ``Fine powder such as clay can be used.'' is corrected to ``Fine powder of clay, glass beads, glass balloons, shirasu balloons, etc. can be used.''that's all

Claims (1)

【特許請求の範囲】[Claims] 非結晶性透明合成樹脂シートに平均粒径0.1〜10μ
mの微粉末を20〜60重量%含有する合成樹脂シート
が積層されかつ非結晶性透明合成樹脂シートのガラス転
移温度以上で該非結晶性透明合成樹脂シートの粘度が微
粉末含有合成樹脂シートの粘度より小さい状態に加熱さ
れている積層シートを、シート表面から圧縮し、冷却後
該積層シートを剥離することを特徴とするノングレアシ
ートの成形法
Amorphous transparent synthetic resin sheet with average particle size of 0.1 to 10μ
Synthetic resin sheets containing 20 to 60% by weight of fine powder of m are laminated, and the viscosity of the amorphous transparent synthetic resin sheet is equal to or higher than the glass transition temperature of the amorphous transparent synthetic resin sheet. A method for forming a non-glare sheet, characterized by compressing a laminated sheet heated to a smaller size from the sheet surface, and peeling off the laminated sheet after cooling.
JP59238544A 1984-11-14 1984-11-14 Molding method of non-glare sheet Pending JPS61118236A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59238544A JPS61118236A (en) 1984-11-14 1984-11-14 Molding method of non-glare sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59238544A JPS61118236A (en) 1984-11-14 1984-11-14 Molding method of non-glare sheet

Publications (1)

Publication Number Publication Date
JPS61118236A true JPS61118236A (en) 1986-06-05

Family

ID=17031827

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59238544A Pending JPS61118236A (en) 1984-11-14 1984-11-14 Molding method of non-glare sheet

Country Status (1)

Country Link
JP (1) JPS61118236A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5234648A (en) * 1990-06-05 1993-08-10 General Electric Company Method of coextruding a plate-shaped product
US5258215A (en) * 1990-06-05 1993-11-02 General Electric Company Method of coextruding a plate-shaped product and the products thus obtained

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5234648A (en) * 1990-06-05 1993-08-10 General Electric Company Method of coextruding a plate-shaped product
US5258215A (en) * 1990-06-05 1993-11-02 General Electric Company Method of coextruding a plate-shaped product and the products thus obtained

Similar Documents

Publication Publication Date Title
US4668729A (en) Process for compression molding of thermoplastic resin and moldings molded by said process
EP0083495B1 (en) Lustrous satin appearing, opaque film compositions and method of preparing same
DE60017939T2 (en) THERMOPLASTIC COMPOSITIONS OF HIGH DIMENSIONAL STABILITY
JPS5995137A (en) Pasted composite body
JPH03142401A (en) Synthetic resin layer, light transmission and diffusion plate and production thereof
JPH06340029A (en) Laminate consisting of glass film and resin
US6147162A (en) Acrylic film and moldings made using the same
JPS63202409A (en) Method for peeling off laminated film
CA1061973A (en) Matt and scratch-resistant films and process for their manufacture
US4148955A (en) Matt and scratch-resistant films and process for their manufacture
JPS61118236A (en) Molding method of non-glare sheet
CN103003067A (en) Reflective material
JP5316240B2 (en) Matte resin film
JP3290136B2 (en) Heat shrinkable polystyrene laminate film
TW454028B (en) Laminated extruded resin sheet
JP3172137B2 (en) Heat shrinkable polystyrene laminated film
JP2020535984A (en) Material extrusion on compatible thermoplastic film 3-D printing
US3555136A (en) Process for the production of a porous sheet
JP2814496B2 (en) Polyester composite film
JPH0155087B2 (en)
JPH0222637A (en) Novel screen
JP4069598B2 (en) Matte film for overlaminate
JP3734381B2 (en) Heat shrinkable polystyrene film
WO1996006127A1 (en) Styrenic resin sheet and molding
JP3162020B2 (en) Heat shrinkable polystyrene-based laminated film