JPS60135225A - Transparent acrylic resin film with non-shining surface - Google Patents

Transparent acrylic resin film with non-shining surface

Info

Publication number
JPS60135225A
JPS60135225A JP58243685A JP24368583A JPS60135225A JP S60135225 A JPS60135225 A JP S60135225A JP 58243685 A JP58243685 A JP 58243685A JP 24368583 A JP24368583 A JP 24368583A JP S60135225 A JPS60135225 A JP S60135225A
Authority
JP
Japan
Prior art keywords
film
acrylic resin
exceeds
less
particles
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
JP58243685A
Other languages
Japanese (ja)
Inventor
Masao Hayashi
林 征男
Takeo Ishihara
石原 武夫
Kuniaki Sakamoto
坂本 国昭
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 Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP58243685A priority Critical patent/JPS60135225A/en
Publication of JPS60135225A publication Critical patent/JPS60135225A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • 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
    • B29K2033/00Use of polymers of unsaturated acids or derivatives thereof as moulding material
    • 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
    • B29K2995/0024Matt surface
    • 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)
  • Extrusion Moulding Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To obtain a transparent acrylic resin film excellent in a matte characteristic, by mixing a rubber modified acrylic resin composition having a specific melt flow index and talc containing 1wt% or less of particles of which the particle size exceeds a specific one in a specific compounding ratio and subsequently forming the resulting mixture into a film by a melt extrusion process. CONSTITUTION:1-10wt% of talc containing 1wt% or less of particles, of which the particle size exceeds 10mum, is mixed with 99-90wt% of a rubber modified acrylic resin composition of which the melt flow index MI is 0.6-20g/10min and the resulting mixture is formed into a film by melt extrusion process to obtain a transparent matte acrylic resin film. A resin with MI of below 0.6g/10min can not be continuously formed into a film with a thickness of 50mum or less and, when MI exceeds 20g/10min, the stable formation of a film becomes difficult because draw-down from a die at the time of melt extrusion is large. When the content of particles with a particle size exceeding 10mum exceeds 1wt%, the film forming property of the film becomes poor and continuous film formation is difficult. Further, when the content of talc is below 1wt%, sufficient matte effect is not obtained and, when exceeds 10wt%, the film forming property or mechanical strength of the film is lowered.

Description

【発明の詳細な説明】 本発明は、透明で艶消し特性にすぐれたアクリル樹脂フ
ィルムに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an acrylic resin film that is transparent and has excellent matte properties.

アクリル樹脂フィルムは、その透明性や耐候性。Acrylic resin film is known for its transparency and weather resistance.

表面光沢等のすぐれた特性を利用して、従来から広く使
用されている。しかし、最近表面光沢のない艶消しされ
たアクリル樹脂フィルムへの要求が高まっている。とく
に、表面反射を嫌う用途の被覆材として、たとえば塩化
ビニール系壁紙の被覆や家具材の被覆などへの用途が期
待されている。
It has been widely used due to its excellent properties such as surface gloss. However, recently there has been an increasing demand for matte acrylic resin films with no surface gloss. In particular, it is expected to be used as a coating material for applications that dislike surface reflection, such as coating vinyl chloride wallpaper and furniture materials.

ところが、アクリル樹脂フィルムに適した艶消し剤が少
ないため、外観的に優れた艶消しフィルムが得られにく
いのが実状である。 □従来技術として、たとえば特開
昭58−23973に、平均粒子径1〜500μの高分
子系艶消剤の使用が提案されている。しかし、平均粒子
径が50μを越え、ると、溶融押出製膜した場合フィル
ム面に肌荒れが生じる。そのため、優れた風合いの艶消
しフィルムを得るためには、平均粒子径1〜50μの艶
消剤が必要である。ところが艶消し剤とし゛ての高分子
架橋粒子の製造を乳化重合で行なった場合は1μ以上の
粒子を得るのは困難であり、懸濁重合で行なった場合は
50μ以下の粒子を得るのは極めて困難であるため実用
性に問題がある。
However, since there are few matting agents suitable for acrylic resin films, it is difficult to obtain matte films with excellent appearance. □As a prior art, for example, Japanese Patent Laid-Open No. 58-23973 proposes the use of a polymer matting agent having an average particle size of 1 to 500 μm. However, if the average particle diameter exceeds 50 μm, roughness will occur on the film surface when the film is formed by melt extrusion. Therefore, in order to obtain a matte film with excellent texture, a matting agent with an average particle size of 1 to 50 μm is required. However, when producing crosslinked polymer particles as a matting agent by emulsion polymerization, it is difficult to obtain particles of 1μ or more, and when using suspension polymerization, it is extremely difficult to obtain particles of 50μ or less. Since it is difficult, there is a problem in practicality.

本発明は、このような背景からなされたものであり、そ
の目的は透明で艶消し特性に優れたアクリル樹脂フィル
ムを得ることにある。
The present invention was made against this background, and its purpose is to obtain an acrylic resin film that is transparent and has excellent matte properties.

すなわち、本発明によるアクリル樹脂フィルムは、メル
トフローインデックス(以下MIと略す。
That is, the acrylic resin film according to the present invention has a melt flow index (hereinafter abbreviated as MI).

測定条件230℃、3soog)が0.6g710分以
上20 、ji’ 710分以下のゴム変性アクリル樹
脂組成物99〜9oiQ%亀に、粒径10μを越える粒
子の含有量が1重量係(以下wt%)以下であるタルク
を1〜10wt%混合し溶融押出製膜することによりイ
()られる。
Measurement conditions: 230°C, 3 soog) is 0.6 g for 710 minutes or more, ji' 710 minutes or less. %) or less by mixing 1 to 10 wt% of talc and forming a film by melt extrusion.

フィルムの厚さは用途によって異るか、一般に好ましい
範囲は20μ〜100μ、より好ましくは25μ〜75
μである。
The thickness of the film varies depending on the application, and the generally preferred range is 20μ to 100μ, more preferably 25μ to 75μ
μ.

本発明において使用されるゴム変性アクリル樹脂組成物
としては、メタクリル酸メチルを主成分とするアクリル
系ゴムを含有する樹脂組成物である。たとえば、特公昭
55−27576、特開昭53−38554 、%開昭
57−200412などに示されるようなアクリル系多
段重合体とメタクリル樹脂とのブレンド物から成る樹脂
組成物があげられる。
The rubber-modified acrylic resin composition used in the present invention is a resin composition containing an acrylic rubber containing methyl methacrylate as a main component. For example, there are resin compositions comprising a blend of an acrylic multistage polymer and a methacrylic resin, as disclosed in Japanese Patent Publication No. 55-27576, Japanese Patent Application Laid-open No. 53-38554, and % Japanese Patent Publication No. 57-200412.

このような樹脂組成物を使用して連続して製膜する場合
、そのMIは0.L!9/lo分以上20g710分以
下であることが必要である。MIが0.6g710分未
満の樹脂では50μ以下の薄いフィルムを連続して製膜
することはできない。捷だMIが20g/lo分を越え
ると溶融押出時にグイからのドローダウンが大きいため
安定して製膜することが困難になる。
When continuously forming films using such a resin composition, the MI is 0. L! It is necessary that the time is 9/lo minutes or more and 20g710 minutes or less. With a resin having an MI of less than 0.6 g and 710 minutes, it is not possible to continuously form a thin film of 50 μm or less. If the raw MI exceeds 20 g/lo, it becomes difficult to stably form a film due to large drawdown from the goo during melt extrusion.

本発明で使用される艶消剤としては、その使用用途によ
り、フィルムの表面光沢を消し、かつ、被被覆物の模様
や柄が見える透明性を兼ね備えさせるものでなくてはな
らない。また、アクリル樹脂の有す、る特徴例えば耐候
性を阻害するものであってはならず、フィルムの製膜性
2強度等多くの条件を満足する必要がある。本発明者ら
はこれらの諸条件を満足する艶消剤について鋭意検討し
た結果、粒径1Oμを越える粒子の含有量が1wt%以
下であるタルクを1〜10wt%、好ましくは、1〜g
wt%混合することで本発明の目的に合致するフィルム
が得られることを発見した。粒径10μを越える粒子が
1wt1に越えるとフィルムの製膜性が悪化し、連続的
な製膜は難しい。また、タルクの含有量が1wt%未満
では充分な艶消し効果が得られず、10wt% を越え
るとフィルムの製膜性や機械的強度が低下する。また、
8〜10wt%の範囲ではほとんど艶消し効果は変化し
ないので、コスト等の点からタルクの含有量は1〜8 
wt%の範囲が好ましい。
Depending on the intended use, the matting agent used in the present invention must be able to eliminate the surface gloss of the film and have transparency that allows the patterns and patterns of the object to be coated to be seen. Furthermore, it must not impede the characteristics of acrylic resins, such as weather resistance, and must satisfy many conditions such as film formability and 2 strength. As a result of intensive study by the present inventors on a matting agent that satisfies these conditions, we found that 1 to 10 wt%, preferably 1 to 1 g of talc containing 1 wt% or less of particles with a particle size exceeding 10μ
It has been discovered that a film meeting the objectives of the present invention can be obtained by mixing wt%. If particles with a particle size exceeding 10 μm exceed 1wt1, the film formability deteriorates and continuous film formation becomes difficult. Further, if the talc content is less than 1 wt%, a sufficient matting effect cannot be obtained, and if it exceeds 10 wt%, the film formability and mechanical strength of the film will decrease. Also,
Since the matting effect hardly changes in the range of 8 to 10 wt%, the talc content should be 1 to 8 wt% from the viewpoint of cost etc.
A range of wt% is preferred.

ものの方がフィルム強度の面からは好ましい。これは、
シランカップリング剤がゴム変性アクリル樹脂組成物と
の親和性を高めるためである。
It is preferable from the viewpoint of film strength. this is,
This is because the silane coupling agent increases the affinity with the rubber-modified acrylic resin composition.

香、 シラン八カップリング剤としては、通常のものが用い得
る。例えばナイロン、ポリアセタールなどのエンジニア
リング樹脂の強化剤として用いられるガラス繊維、ガラ
スピーズなどの表面処理剤として用いられる、公知のシ
ランカップリング剤が好ましく用いられる。
As the silane coupling agent, ordinary ones can be used. For example, a known silane coupling agent is preferably used, which is used as a surface treatment agent for glass fibers, glass beads, etc., which is used as a reinforcing agent for engineering resins such as nylon and polyacetal.

又、本発明に市川なシランカッシリング剤として、アル
コキシシラン(例えば、アルキルトリアルコキシシラン
)なども好ましく用いられる。
Also, alkoxysilanes (eg, alkyltrialkoxysilanes) are preferably used as silane cassilling agents in the present invention.

フィルムの製法については、溶融押出製膜で作られ、T
ダイ法、インフレーション法等の通常の方法で製膜する
ことができる。
Regarding the manufacturing method of the film, it is made by melt extrusion film forming, and T
The film can be formed by a conventional method such as a die method or an inflation method.

以下実施例により本発明を説明する。The present invention will be explained below with reference to Examples.

実施例で用いた評価方法を以下に示す。The evaluation method used in the examples is shown below.

(1) 製膜性 ○:Tダイ法で25μの厚さのフィルムを安定して製膜
できる。
(1) Film-forming property ○: A film with a thickness of 25 μm can be stably formed using the T-die method.

△:Tダイ法で50μの厚さのフィルムを安定して製膜
できる。
Δ: A film with a thickness of 50 μm can be stably formed using the T-die method.

×:、Tダイ法で50μの厚さのフィルムの製膜が困難
×: It is difficult to form a film with a thickness of 50 μm using the T-die method.

(2)光学特性 艶消し性;ASTM 02157の試験法による45′
光沢度(グロス)の値 ○:光沢度の値が60%未満 △:光沢度の値が60〜80係 ×:光沢度の値が80%を越える。
(2) Optical properties Matting property: 45' according to ASTM 02157 test method
Glossiness value ○: Glossiness value is less than 60% Δ: Glossiness value is 60-80 x: Glossiness value exceeds 80%.

透明性;ASTM D1003の試験法による曇り度(
ヘーズ)の値 ○:曇り度の値が60%未満 △:曇り度の値が60〜80係 ×:曇り度の値が80係を越える。
Transparency: Haze (according to ASTM D1003 test method)
Haze) value ○: Haze value is less than 60% Δ: Haze value is 60-80% ×: Haze value is over 80%.

(3)機械的特性 引張強さ; ASTM D882の試験法による。(3) Mechanical properties Tensile strength: Based on ASTM D882 test method.

○:引張強さ2−oKy/−を越える △:引張強さ1.5〜Z 0 K5i/mA×:引張強
さ1.sKy/−未満。
○: Tensile strength exceeds 2-oKy/- △: Tensile strength 1.5 to Z 0 K5i/mA×: Tensile strength 1. Less than sKy/-.

実施例1.比較例1 特開昭57−200412の実施例1に従って乳化重合
により製造した第1層がメチルメタクリレート(以下M
MAと略す)を主成分とした硬質重合体、第2層がアル
ギルメタクリレートを主成分としたアクリルゴム重合体
、第3層がMMAを主成分とした硬質重合体である多段
ゴム弾性体組成物とMMA 88wt% 、メチルアク
リレート12wt%でMI=12のメタクリル樹脂とを
30ニア00割合で混合した混合物(MI=41にメル
ク(日本タルク@製)を加えて混合しスクリュー型押出
機を通してペレット化した。
Example 1. Comparative Example 1 The first layer produced by emulsion polymerization according to Example 1 of JP-A-57-200412 was methyl methacrylate (hereinafter referred to as M
A multi-stage rubber elastic body composition in which the second layer is an acrylic rubber polymer mainly composed of argyl methacrylate, and the third layer is a hard polymer mainly composed of MMA. A mixture of 88 wt% MMA, 12 wt% methyl acrylate, and a methacrylic resin with an MI of 12 at a ratio of 30 to 00 (MI = 41 and Merck (manufactured by Nippon Talc@) was mixed and passed through a screw extruder into pellets. It became.

さらに、このペレットを樹脂温度(ダイの出口)と約2
40℃に特定した押出機を通してTダイ法により、引き
とり速度4m/分で巾700mm+厚さ25μのフィル
ムに製膜した。タルクの径および量は表1に不す組み合
わせで作成し評価した。
Furthermore, this pellet is adjusted to a temperature of approximately 2
A film having a width of 700 mm and a thickness of 25 μm was formed by passing through an extruder specified at 40° C. and using a T-die method at a drawing speed of 4 m/min. The diameter and amount of talc were prepared and evaluated in different combinations as shown in Table 1.

本発明品は製膜性、光学特性9機械的特性のいずれも優
れたフィルムが得られるのに対し、メルクの量が1wt
%未満のもの(比較例(1))は艶消しが不足し、また
タルクの量が10wt係を越えるもの(比較例(iil
 )は機械的強度が不足して、商品価値の著しく低いフ
ィルムでおった。また、メルクの粒径が10μ以上のも
のを1wt%以上含むもの(比較例(iii) )は、
50μのフィルムを安定して製膜することができなかっ
た。
With the product of the present invention, a film with excellent film formability, optical properties, and mechanical properties can be obtained, whereas the amount of Merck is 1 wt.
% (Comparative Example (1)), the matting effect is insufficient, and the amount of talc exceeds 10wt (Comparative Example (IIL)).
) was a film with extremely low commercial value due to lack of mechanical strength. In addition, those containing 1 wt% or more of Merck particles with a particle size of 10 μ or more (Comparative Example (iii)):
It was not possible to stably form a 50μ film.

比較例2 実施例1と同様にして、多段ゴム弾性体組成物と市販の
メタクリル樹脂(無化成工業■製デルペツ)8ON)と
をso:soの割合で混合した混合物(M I 0.2
.!ii’/10分)100重量部に対して、タルク(
m径10μを越える粒子を含まないもの)を5部加えて
混合し押出機を通してペレタイズ後、Tダイ法で製膜し
た。50μより薄いフィルムを製膜しようとすると、樹
脂切れが多発して安定した製膜ができなかった。
Comparative Example 2 In the same manner as in Example 1, a mixture (M I 0.2) was prepared by mixing a multistage rubber elastic body composition and a commercially available methacrylic resin (Delpetsu 8ON, manufactured by Mukasei Kogyo ■) at a ratio of so:so.
.. ! ii'/10 minutes) to 100 parts by weight of talc (
5 parts of the mixture (not containing particles with a diameter exceeding 10 μm) were added and mixed, pelletized through an extruder, and then formed into a film using the T-die method. When attempting to form a film thinner than 50 μm, resin breakage occurred frequently and stable film formation was not possible.

実施例2.比較例3 実施例1で使用した混合物Iに、粒径10μを越える粒
子を含まないタルク、マイカ、硫酸バリウムを1〜10
wt係加えて混合し押出機を通してペレタイズ後Tダイ
法で製膜した。製膜性は硫酸・ζリウム以外は全て良好
だった。硫酸バリウムを加えたものは、厚みが25μ以
下になると安定した製膜ができなかった。その他の艶消
剤を富むフィルムについて、光学的特性を評価した。第
1図に示すように、光沢度と曇り度がともに良好なもの
はタルクを入れたものだけだった。
Example 2. Comparative Example 3 To the mixture I used in Example 1, 1 to 10% of talc, mica, and barium sulfate, which do not contain particles with a particle size exceeding 10μ, are added.
After adding wt and mixing, pelletizing through an extruder, a film was formed by a T-die method. The film forming properties were all good except for sulfuric acid and ζlium. When barium sulfate was added, stable film formation was not possible when the thickness was less than 25 μm. Other matting agent enriched films were evaluated for optical properties. As shown in FIG. 1, the only one with good gloss and haze was the one containing talc.

実施例3 実施例1で使用した混合物工にメルクを3%混合したも
の(本発明品l)と、該タルクを長鎖アルキル(C16
〜CI8と推定される)トリエトキシシラン(太へ化学
■製:商品番号RT−168E)Th用いて通常の方法
で表面処理を施したものと3wt%混合したもの(本発
明品4)を、それぞれ押出機ヲ通してペレタイズ後Tダ
イ法で厚さ25μのフィルムを製膜した。製膜性や光学
的特性は本発明品19本発明品4ともに同等であったが
、開帳強度は本発明品1がZ9に−P/−であるのに対
して、本発明品4は3.81’−p/−であり、約30
%上昇した。
Example 3 The mixture used in Example 1 was mixed with 3% Merck (invention product 1), and the talc was mixed with long chain alkyl (C16
A mixture of 3 wt% of triethoxysilane (estimated to be ~CI8) (manufactured by Taihe Kagaku ■: product number RT-168E) by a conventional method using Th (product of the present invention 4), After pelletizing through an extruder, a film with a thickness of 25 μm was formed using a T-die method. The film formability and optical properties were the same for Invention Product 19 and Invention Product 4, but the opening strength of Invention Product 1 was -P/- for Z9, while Invention Product 4 was 3. .81'-p/-, about 30
%Rose.

以下余白Margin below

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

第1図、実施例と比較例との結果を図示した。 lはマイカを1 wt%ないし10wt%混合したとき
の光沢度と曇!llvとの変化を示す。 2は、タルクについての変化を示す。 特許出願人 旭化成工業式会社
FIG. 1 illustrates the results of Examples and Comparative Examples. l is the gloss and cloudiness when 1 wt% to 10 wt% of mica is mixed! It shows the change from llv. 2 shows changes regarding talc. Patent applicant Asahi Kasei Kogyo Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 1、 メルトフローインデックスが0.6.9/10分
以上20g/io分以下のゴム変性アクリル樹脂組成物
99〜90重量係と、粒径10μを越える粒子の含有量
が1重量係以下であるタルク1〜10重量係とを混合し
、次いで溶融押出製膜したことを特徴とする透明艶消し
アクリル樹脂フていることを特徴とする特許請求の範囲
第1項記載のアクリル樹脂フィルム
1. A rubber-modified acrylic resin composition with a melt flow index of 0.6.9/10 min or more and 20 g/io min or less, with a content of 99 to 90 parts by weight, and a content of particles with a particle size exceeding 10 μm not more than 1 part by weight. The acrylic resin film according to claim 1, characterized in that it contains a transparent matte acrylic resin film, which is obtained by mixing 1 to 10 parts by weight of talc and then melt-extruding the film.
JP58243685A 1983-12-26 1983-12-26 Transparent acrylic resin film with non-shining surface Pending JPS60135225A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58243685A JPS60135225A (en) 1983-12-26 1983-12-26 Transparent acrylic resin film with non-shining surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58243685A JPS60135225A (en) 1983-12-26 1983-12-26 Transparent acrylic resin film with non-shining surface

Publications (1)

Publication Number Publication Date
JPS60135225A true JPS60135225A (en) 1985-07-18

Family

ID=17107460

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58243685A Pending JPS60135225A (en) 1983-12-26 1983-12-26 Transparent acrylic resin film with non-shining surface

Country Status (1)

Country Link
JP (1) JPS60135225A (en)

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