JPH031349B2 - - Google Patents

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Publication number
JPH031349B2
JPH031349B2 JP7957081A JP7957081A JPH031349B2 JP H031349 B2 JPH031349 B2 JP H031349B2 JP 7957081 A JP7957081 A JP 7957081A JP 7957081 A JP7957081 A JP 7957081A JP H031349 B2 JPH031349 B2 JP H031349B2
Authority
JP
Japan
Prior art keywords
mol
synthetic resin
weight
glass
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP7957081A
Other languages
Japanese (ja)
Other versions
JPS57195153A (en
Inventor
Taku Uchigaki
Fukashi Hashimoto
Masayuki Egami
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Petrochemical 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 Mitsubishi Petrochemical Co Ltd filed Critical Mitsubishi Petrochemical Co Ltd
Priority to JP7957081A priority Critical patent/JPS57195153A/en
Publication of JPS57195153A publication Critical patent/JPS57195153A/en
Publication of JPH031349B2 publication Critical patent/JPH031349B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、ブロツキング性を改良したフイルム
に関し、さらに詳しくはガラス粉末を添加するこ
とにより透明性を阻害せずにブロツキング性と滑
り性を改良したフイルムに関する。 今日、透明性合成樹脂フイルムは、各種包装用
袋、カバー、ラツプ等に広く使用されている。こ
れ等のフイルムは、それ自体が有する優れた透明
性、表面光沢等により内容物が美しく見えて商品
価値を上げる反面、表面が平滑であるために、フ
イルムとフイルムが付着し易く(ブロツキングと
呼ばれる。)、また、使いにくい欠点がある。 このブロツキングの改良のため、二酸化ケイ
素、炭酸カルシウム等の無機の微粉末を添加して
表面凹凸を若干形成することによりブロツキング
を防止することが行なわれている。 しかしながらこれらの無機微粉末は透明性を阻
害する欠点を有するため、添加量を多くすること
ができない。 また、透明性の低下を防止するために非常に微
細にしているため、分散性が悪く凝集しやすいこ
とや、帯電防止剤、滑り剤等他の添加剤を吸着し
て帯電防止、滑り性等の効果を阻害すること等の
問題を有し、品質設計が難しく、全ての性能を同
時に満足させることができなかつた。 本発明はこれらの問題を解決するブロツキング
防止剤を提供するものである。すなわちベースの
透明性合成樹脂に合わせた屈折率を持つガラスを
微粉末にして添加することにより、フイルムにし
た場合に透明性を低下させることがなく、かつ、
他の添加剤の効果も阻害せずに充分なブロツキン
グ防止効果をあげる技術を提供するものである。 本発明に使われる透明性合成樹脂は、フイルム
に成形して透明性のある樹脂ならば何でも良くポ
リエチレン、ポリプロピレン、エチレン酢酸ビ共
重合体等のポリオレフイン、ポリエステル、ポリ
アミド、ポリ塩化ビニル、ポリビニルアルコール
等があげられる。 本発明におけるガラスとは、二酸化ケイ素を主
要成分とし、二酸化ケイ素を5〜80モル%、アル
カリ金属酸化物を1〜50モル%、アルカリ土類金
属酸化物を0〜40モル%、Al2O3、B2O3、P2O5
ZnO、TiO2又はBi2O3より選ばれる酸化物の1種
又は2種以上を計0〜50モル%含むガラス質物質
が使用される。 ここで二酸化ケイ素は主要成分としてガラスの
構造の骨格を形成し、酸化アルミニウムはガラス
の化学的耐久性を向上させる。他の成分はガラス
形成を助け、屈折率の調整やガラスを微粉末にし
やすいようにもろくさせる等の効果を持つ。 このガラスは樹脂に添加しやすいように微粉末
の状態にされ、その平均粒径は50μ以下、好まし
くは20μ以下とされる。また、1μ以下ではブロツ
キング防止効果が少なく、重量比で少なくとも半
分以上は1μ以上であることが望ましい。ガラス
粉末の表面積については、他の添加剤の吸着を防
ぐ意味から小さいほうが望ましく、ガラス重量当
りの表面積として50m2/g以下好ましくは5m2
g以下になるように粉末化される。 これらの粉末は、場合によつてはパラフイン、
脂肪酸、多価アルコール、シランカツプリング剤
等の表面処理剤で処理してもよくかかる処理をし
た粉末は合成樹脂中への分散性が改良される。 本発明におけるガラス微粉末の添加量は、樹脂
の種類、フイルムへの成形法によつて異なるが、
一般に、合成樹脂とガラス微粉末の合計量を基準
として、0.05重量%以上、1.0重量%未満、好ま
しくは、0.2重量%以上、1.0重量%未満が添加さ
れ、ブロツキングしやすい樹脂組成物の場合多め
に、延伸フイルム等では少なめの量でより微細な
粉末が使用される。 従来のブロツキング防止剤の場合、透明性の低
下や他の添加剤の吸着を軽減するため、一般に
0.2重量%以下の量が添加されており、樹脂組成
物によつてはブロツキング防止性能が充分でない
ことがあつたが、本発明のガラス微粉末は他の性
能への影警が少ないため、ブロツキング防止に必
要な量を添加することができ、また、同一のブロ
ツキング防止性能を得るためには、添加量を少な
くすることができる。なぜならば、透明性にほと
んど影響を与えずしてブロツキング防止に最も効
果のある粒径を選ぶことができるからである。 本発明における成形は種々の方法により行なう
ことができる。透明性合成樹脂に本発明によるガ
ラス微粉末を必要に応じ他の添加剤とともに直接
添加して成形してもよく、また、一度高濃度のマ
スターバツチにしてから樹脂で希釈して成形して
もよい。フイルム成形法としてはインフレーシヨ
ン成形法、Tダイ成形法、二軸延伸成形法、カレ
ンダー成形法等公知の成形法を使用することがで
きる。 本発明のフイルムはブロツキングが防止され透
明性が良く、帯電防止剤や滑り剤との組み合わせ
による効果が優れるために種々の用途に使用する
ことができる。例えば、食品や衣料の包装袋とし
て使用すればブロツキングが防止されているた
め、充填作業がスムーズに行なわれ、また、帯電
防止剤及び滑り剤の効果を阻害しないために帯電
付着が少なく、滑りが良く、透明性が良いことか
ら商品価値を上げることができる。 また、従来エチレン酢酸ビニルコポリマー等ブ
ロツキング防止がしにくかつたフイルムに使用す
ることにより効果的にブロツキング防止をするこ
とができる。 次に実施例を用いて本発明を説明するが本発明
はこれに限定されるものではない。 実施例 1 ガラス組成が、SiO235モル%、Al2O35モル%、
P2O515モル%、Na2O20モル%、MgO15モル%、
ZnO10モル%で、平均粒径が表−1であるガラス
微粉末を用意し低密度ポリエチレン(三菱油化製
ユカロンZF−51)に濃度を変化させて添加し厚
さ50μのフイルムをインフレーシヨン法で成形し
た。
The present invention relates to a film with improved blocking properties, and more particularly to a film with improved blocking properties and slipperiness without impairing transparency by adding glass powder. Today, transparent synthetic resin films are widely used for various packaging bags, covers, wraps, etc. These films have excellent transparency and surface gloss, which makes the contents look beautiful and increase the product value. However, because the surface is smooth, films tend to stick to each other (a phenomenon called blocking). ), it also has the disadvantage of being difficult to use. In order to improve this blocking, inorganic fine powder such as silicon dioxide or calcium carbonate is added to form some surface irregularities to prevent blocking. However, since these inorganic fine powders have the disadvantage of impairing transparency, it is not possible to increase the amount added. In addition, since it is made very fine to prevent a decrease in transparency, it has poor dispersibility and is prone to agglomeration, and it also adsorbs other additives such as antistatic agents and slipping agents, resulting in antistatic and slippery properties. However, quality design was difficult, and it was not possible to satisfy all performance requirements at the same time. The present invention provides an antiblocking agent that solves these problems. In other words, by adding glass with a refractive index that matches the base transparent synthetic resin in the form of fine powder, the transparency will not decrease when it is made into a film, and
The purpose of this invention is to provide a technology that achieves a sufficient anti-blocking effect without interfering with the effects of other additives. The transparent synthetic resin used in the present invention may be any transparent resin that can be formed into a film, such as polyethylene, polypropylene, polyolefin such as ethylene-biacetate copolymer, polyester, polyamide, polyvinyl chloride, polyvinyl alcohol, etc. can be given. In the present invention, glass is a material whose main component is silicon dioxide, 5 to 80 mol% of silicon dioxide, 1 to 50 mol% of alkali metal oxides, 0 to 40 mol% of alkaline earth metal oxides, and Al 2 O. 3 , B2O3 , P2O5 ,
A glassy material containing a total of 0 to 50 mol % of one or more oxides selected from ZnO, TiO 2 or Bi 2 O 3 is used. Here, silicon dioxide forms the framework of the glass structure as the main component, and aluminum oxide improves the chemical durability of the glass. Other components assist in glass formation and have effects such as adjusting the refractive index and making the glass brittle so that it can be easily ground into fine powder. This glass is made into a fine powder so that it can be easily added to the resin, and its average particle size is 50μ or less, preferably 20μ or less. Further, if it is less than 1μ, the anti-blocking effect will be small, so it is desirable that at least half of the weight ratio is 1μ or more. As for the surface area of the glass powder, it is preferable that it is small in order to prevent adsorption of other additives, and the surface area per glass weight is 50 m 2 /g or less, preferably 5 m 2 /g.
It is powdered to a weight of less than 100 g. These powders sometimes contain paraffin,
The powder may be treated with a surface treatment agent such as a fatty acid, a polyhydric alcohol, or a silane coupling agent, and the dispersibility of the powder into a synthetic resin will be improved. The amount of glass fine powder added in the present invention varies depending on the type of resin and the method of forming into a film, but
Generally, based on the total amount of synthetic resin and glass fine powder, 0.05% by weight or more and less than 1.0% by weight, preferably 0.2% by weight or more and less than 1.0% by weight is added, and this is often the case for resin compositions that are prone to blocking. In contrast, smaller amounts of finer powder are used in stretched films and the like. Conventional antiblocking agents are generally used to reduce transparency and adsorption of other additives.
However, the fine glass powder of the present invention has less effect on other properties, so it has less blocking prevention properties. The amount necessary for prevention can be added, and the amount added can be reduced in order to obtain the same anti-blocking performance. This is because it is possible to select the particle size that is most effective in preventing blocking without substantially affecting transparency. Molding in the present invention can be carried out by various methods. The glass fine powder according to the present invention may be directly added to a transparent synthetic resin along with other additives if necessary and molded, or it may be formed into a highly concentrated masterbatch and then diluted with resin and molded. . As the film molding method, known molding methods such as inflation molding, T-die molding, biaxial stretching molding, and calendar molding can be used. The film of the present invention prevents blocking, has good transparency, and has excellent effects when combined with antistatic agents and slip agents, so it can be used for various purposes. For example, when used as packaging bags for food or clothing, blocking is prevented, so filling operations can be carried out smoothly, and since the effects of antistatic agents and slip agents are not inhibited, there is less electrostatic adhesion and slippage. Good quality and transparency can increase product value. Furthermore, by using it in films that are difficult to prevent blocking, such as ethylene vinyl acetate copolymers, blocking can be effectively prevented. Next, the present invention will be explained using Examples, but the present invention is not limited thereto. Example 1 Glass composition is 35 mol% of SiO 2 , 5 mol% of Al 2 O 3 ,
P 2 O 5 15 mol%, Na 2 O 20 mol%, MgO 15 mol%,
Prepare fine glass powder containing 10 mol% ZnO and having an average particle size shown in Table 1, add it to low density polyethylene (Yukalon ZF-51 manufactured by Mitsubishi Yuka) at varying concentrations, and make a film with a thickness of 50μ by inflation. Molded by method.

【表】 なお、このガラスの屈折率は1.50、低密度ポリ
エチレンの屈折率は1.51であつた。 実施例 2 実施例1のガラス微粉末(b)をエチレン酢酸ビニ
ルコポリマー(三菱油化製ユカロンエバ、
EVA41H)に0.9重量%添加しインフレーシヨン
成形法により厚さ100μのフイルムを得た。 なお、このエチレン酢酸ビニルコポリマーの屈
折率は1.50であつた。 実施例 3 実施例1のガラス微粉末(c)をポリプロピレン
(三菱油化製ノーブレンFL6)に0.2重量%添加し
二軸延伸法により厚さ30μのフイルムを得た。 なお、ポリプロピレンの屈折率は、1.49であつ
た。 比較例 1 表−2の粒径の二酸化ケイ素、炭酸カルシウ
ム、微粉末を実施例1の低密度ポリエチレンに添
加し厚さ50μのフイルムをインフレーシヨン法で
成形した。
[Table] The refractive index of this glass was 1.50, and the refractive index of low density polyethylene was 1.51. Example 2 The fine glass powder (b) of Example 1 was mixed with ethylene vinyl acetate copolymer (Yukalon Eva manufactured by Mitsubishi Yuka Co., Ltd.).
EVA41H) was added in an amount of 0.9% by weight, and a film with a thickness of 100μ was obtained by inflation molding. Note that the refractive index of this ethylene vinyl acetate copolymer was 1.50. Example 3 0.2% by weight of the glass fine powder (c) of Example 1 was added to polypropylene (Noblen FL6 manufactured by Mitsubishi Yuka Co., Ltd.) and a film with a thickness of 30 μm was obtained by biaxial stretching. Note that the refractive index of polypropylene was 1.49. Comparative Example 1 Silicon dioxide, calcium carbonate, and fine powder having the particle sizes shown in Table 2 were added to the low-density polyethylene of Example 1, and a film having a thickness of 50 μm was formed by an inflation method.

【表】 なお、この二酸化ケイ素の屈折率は1.45、炭酸
カルシウムの屈折率は1.60であつた。 比較例 2 比較例1で用いた微粉末(e)を実施例2で用いた
エチレン酢酸ビニルコポリマーに0.3重量%と0.9
重量%を夫々添加した厚さ100μのフイルムを得
た。 比較例 3 比較例1で用いた微粉末(d)を用い実施例3のよ
うにポリプロピレン、0.1重量%と0.2重量%を
夫々添加し二軸延伸フイルムを得た。 各フイルムの霞み度、ブロツキング性を表−3
に示す。表3より本発明の優れたブロツキング防
止、透明性は明らかである。 なお、ブロツキング性は、フイルムを巾2cmの
短冊状とし二枚を長さ5cm重ね50g/cm2の荷重を
かけ40℃で24時間放置後引つ張り試験機でせん断
剥離する時の荷重を読み取つて評価した。数値の
少ない方が優れる。 実施例4、比較例4 実施例3、比較例3で用いた材料で、添加濃度
を0.3重量%とし、帯電防止剤としてアルキルア
ミン(ライオンアーマー製、アモスタツト310)
を0.2重量%、滑り剤としてステアリン酸アミド
を0.1重量%添加し二軸延伸法で作られたフイル
ムを用意した。 帯電防止性については、フイルムを10KVの電
界で帯電させた後電界を0にして帯電減衰の半期
を測定した。滑り性についてはASTMD1894−
73に従いスリツプテスターで静摩擦係数を測定し
た。表−4にその結果を示す。本発明技術が帯電
防止、滑り性についても従来技術より良いことは
明らかである。 比較例 5 実施例1のガラス組成のうちP2O5のかわりに
PbOに置きかえた他は同様にフイルムを成形し
た。このガラスの屈折率は1.58で平均粒径は2μで
あつたが表−3のように実施例1に比べ透明性が
劣つた。
[Table] The refractive index of silicon dioxide was 1.45, and the refractive index of calcium carbonate was 1.60. Comparative Example 2 The fine powder (e) used in Comparative Example 1 was added to the ethylene vinyl acetate copolymer used in Example 2 at 0.3% by weight and 0.9% by weight.
A film with a thickness of 100 μm was obtained in which % by weight of each was added. Comparative Example 3 Using the fine powder (d) used in Comparative Example 1, 0.1% by weight and 0.2% by weight of polypropylene were added as in Example 3 to obtain a biaxially stretched film. Table 3 shows the haze and blocking properties of each film.
Shown below. From Table 3, it is clear that the present invention has excellent blocking prevention and transparency. In addition, blocking property is measured by making two strips of film 2 cm wide, stacking them 5 cm long, applying a load of 50 g/ cm2 , leaving them at 40°C for 24 hours, and then reading the load when shearing and peeling with a tensile tester. I evaluated it. The lower the number, the better. Example 4, Comparative Example 4 The materials used in Example 3 and Comparative Example 3 were added at a concentration of 0.3% by weight, and alkylamine (manufactured by Lion Armor, Amostat 310) was added as an antistatic agent.
A film made by biaxial stretching was prepared by adding 0.2% by weight of stearic acid amide and 0.1% by weight of stearic acid amide as a slip agent. Regarding antistatic properties, the film was charged with an electric field of 10 KV, and then the electric field was reduced to 0 and the half-year of charge decay was measured. Regarding slipperiness, ASTMD1894−
The static friction coefficient was measured using a slip tester according to 73. Table 4 shows the results. It is clear that the technology of the present invention is also better in terms of antistatic properties and slipperiness than the prior art. Comparative Example 5 In place of P 2 O 5 in the glass composition of Example 1
A film was molded in the same manner except that PbO was used instead. This glass had a refractive index of 1.58 and an average particle size of 2 μm, but as shown in Table 3, its transparency was inferior to that of Example 1.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 透明性を有する合成樹脂に、ガラスの微粉末
を0.05重量%以上1.0重量%未満添加してなるブ
ロツキング性を改良した熱可塑性合成樹脂フイル
ム。 2 ガラスの微粉末が、屈折率1.47〜1.55であつ
て、合成樹脂がポリオレフインである特許請求の
範囲第1項記載のブロツキング性を改良した熱可
塑性合成樹脂フイルム。 3 ガラスの微粉末が、二酸化ケイ素を5〜80モ
ル%、アルカリ金属酸化物を1〜50モル%、アル
カリ土類金属酸化物を0〜40モル%及び、
Al2O3、B2O3、P2O5、ZnO、TiO2、又はBi2O3
り選ばれる酸化物の1種又は2種以上を0〜50モ
ル%含有するものである特許請求の範囲第1項記
載のブロツキング性を改良した熱可塑性合成樹脂
フイルム。
[Scope of Claims] 1. A thermoplastic synthetic resin film with improved blocking properties, which is obtained by adding 0.05% by weight or more and less than 1.0% by weight of fine glass powder to a transparent synthetic resin. 2. A thermoplastic synthetic resin film with improved blocking properties as claimed in claim 1, wherein the glass fine powder has a refractive index of 1.47 to 1.55 and the synthetic resin is polyolefin. 3 Fine glass powder contains 5 to 80 mol% of silicon dioxide, 1 to 50 mol% of alkali metal oxide, 0 to 40 mol% of alkaline earth metal oxide, and
A patent claim containing 0 to 50 mol% of one or more oxides selected from Al 2 O 3 , B 2 O 3 , P 2 O 5 , ZnO, TiO 2 , or Bi 2 O 3 A thermoplastic synthetic resin film with improved blocking properties according to item 1.
JP7957081A 1981-05-26 1981-05-26 Thermoplastic synthetic resin film having reduced blocking property Granted JPS57195153A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7957081A JPS57195153A (en) 1981-05-26 1981-05-26 Thermoplastic synthetic resin film having reduced blocking property

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7957081A JPS57195153A (en) 1981-05-26 1981-05-26 Thermoplastic synthetic resin film having reduced blocking property

Publications (2)

Publication Number Publication Date
JPS57195153A JPS57195153A (en) 1982-11-30
JPH031349B2 true JPH031349B2 (en) 1991-01-10

Family

ID=13693652

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7957081A Granted JPS57195153A (en) 1981-05-26 1981-05-26 Thermoplastic synthetic resin film having reduced blocking property

Country Status (1)

Country Link
JP (1) JPS57195153A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0655836B2 (en) * 1990-02-27 1994-07-27 石塚硝子株式会社 Master Badge
JP3396729B2 (en) * 1993-12-22 2003-04-14 住友化学工業株式会社 Polypropylene composition and stretched film thereof
KR20190010740A (en) 2014-03-13 2019-01-30 미쯔비시 케미컬 주식회사 Acrylic resin composition, method for producing same, and acrylic resin film

Also Published As

Publication number Publication date
JPS57195153A (en) 1982-11-30

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