JP2002249622A - Porous film and preparation method for the same - Google Patents
Porous film and preparation method for the sameInfo
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- JP2002249622A JP2002249622A JP2001046928A JP2001046928A JP2002249622A JP 2002249622 A JP2002249622 A JP 2002249622A JP 2001046928 A JP2001046928 A JP 2001046928A JP 2001046928 A JP2001046928 A JP 2001046928A JP 2002249622 A JP2002249622 A JP 2002249622A
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- weight
- porous film
- parts
- density polyethylene
- machine direction
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は多孔性フィルム及び
その製造方法に関する。詳しくは、機械方向の低ひずみ
伸び強度が高くて定ピッチ印刷に適した、透湿度が良好
であり、且つ、風合いも良い多孔性フィルム及びその製
造方法に関する。[0001] The present invention relates to a porous film and a method for producing the same. More specifically, the present invention relates to a porous film which has low mechanical strain and high elongation strength, is suitable for constant pitch printing, has good moisture permeability, and has good texture, and a method for producing the same.
【0002】[0002]
【従来の技術】従来、ポリオレフィン樹脂に無機充填材
および各種油、ワックス等を添加したフィルムを少なく
とも一軸方向に延伸し、無機充填材とポリオレフィンと
の間で界面剥離が起こることによりボイドを発生させ多
孔性フィルムを製造する方法が多数提案されている。こ
れら多孔性フィルムは内部に多数の微小なボイドを有し
ているため、高い透湿度を有しながらも液体を透過させ
ることはない。この性質を生かし、使い捨て紙オムツな
どの衛生材料、建築材料、反射フィルム、電池セパレー
ター等多岐にわたり用いられている。2. Description of the Related Art Conventionally, a film in which an inorganic filler and various oils, waxes, etc. are added to a polyolefin resin is stretched in at least one axial direction, and voids are generated due to interfacial separation between the inorganic filler and the polyolefin. Many methods have been proposed for producing porous films. Since these porous films have a large number of minute voids inside, they do not allow liquid to permeate while having high moisture permeability. Taking advantage of this property, it is widely used in sanitary materials such as disposable diapers, building materials, reflective films, battery separators, and the like.
【0003】使い捨てオムツにおいては、近年さまざま
な印刷を施された多孔性フィルムが使われている。オム
ツの特定部位に印刷を行うことが好まれて実施されてお
り、そのためには、印刷のピッチがずれない必要があ
る。印刷のピッチずれは、印刷時にフィルムが機械方向
に伸びすぎると発生しやすく、伸びの少ないフィルムが
要求されている。[0003] In disposable diapers, porous films which have been subjected to various printings in recent years have been used. Printing is preferably performed on a specific portion of the diaper, and for that purpose, it is necessary that the printing pitch does not shift. The printing pitch deviation is apt to occur when the film is stretched too much in the machine direction during printing, and a film with little stretching is required.
【0004】従来、使い捨てオムツの資材として使用さ
れる多孔性フィルムは柔軟性を良くする観点からポリオ
レフィン樹脂として線形低密度ポリエチレンが専ら用い
られてきた。しかしながら、こうしたフィルムは、柔軟
性には優れるものの、印刷の際にフィルムが伸びてしま
うという欠点がある。また、ピッチずれには機械方向の
熱収縮率が少ないことも良い影響を与える。[0004] Conventionally, as a porous film used as a material for disposable diapers, linear low-density polyethylene has been exclusively used as a polyolefin resin from the viewpoint of improving flexibility. However, although such a film is excellent in flexibility, it has a drawback that the film stretches during printing. Further, a small heat shrinkage in the machine direction also has a good effect on the pitch deviation.
【0005】[0005]
【発明が解決しようとする課題】本発明の目的は、従来
品と同レベルの透湿度を有し、且つ、機械方向の低ひず
み伸び強度に優れ、しかも柔軟性に富み、風合いが良好
である、定ピッチの印刷に適した多孔性フィルムを提供
することにある。SUMMARY OF THE INVENTION An object of the present invention is to have the same level of moisture permeability as a conventional product, to have excellent low strain elongation in the machine direction, to be flexible, and to have a good feeling. To provide a porous film suitable for printing at a constant pitch.
【0006】[0006]
【課題を解決するための手段】本発明者らは、鋭意検討
した結果、ポリオレフィン系樹脂及び無機充填材を含む
多孔性フィルムを製造するに際し、ポリオレフィン系樹
脂として、(1)特定の密度の高密度ポリエチレン及び
ポリプロピレンの少なくとも1種、(2)特定の密度の
線形低密度ポリエチレン、及び、(3)分岐状低密度ポ
リエチレンの3種類の樹脂の特定量を用いることによ
り、上記課題が解決できることを見出し、本発明に到達
した。Means for Solving the Problems As a result of intensive studies, the present inventors have found that, when producing a porous film containing a polyolefin resin and an inorganic filler, the polyolefin resin (1) has a high specific density. It is possible to solve the above problem by using at least one kind of high-density polyethylene and polypropylene, (2) a linear low-density polyethylene of a specific density, and (3) a branched low-density polyethylene of three kinds of specific amounts. Heading, the present invention has been reached.
【0007】すなわち、本発明は、ポリオレフィン系樹
脂25〜55重量%及び無機充填材75〜45重量%を
含む樹脂組成物から成形された多孔性フィルムであっ
て、ポリオレフィン系樹脂が、密度0.930〜0.9
75の高密度ポリエチレン及びポリプロピレンから選ば
れた少なくとも1種の樹脂10〜70重量%、密度0.
905〜0.930の線形低密度ポリエチレン88〜1
5重量%、及び分岐状低密度ポリエチレン2〜15重量
%を含む多孔性フィルムである。That is, the present invention relates to a porous film formed from a resin composition containing 25 to 55% by weight of a polyolefin resin and 75 to 45% by weight of an inorganic filler, wherein the polyolefin resin has a density of 0.1%. 930-0.9
10 to 70% by weight of at least one resin selected from high-density polyethylene and polypropylene having a density of 0.
905 to 0.930 linear low density polyethylene 88-1
It is a porous film containing 5% by weight and 2 to 15% by weight of a branched low-density polyethylene.
【0008】本発明に係わる多孔性フィルムの好ましい
態様として、前記樹脂組成物100重量部に対し、硬化
ひまし油及び脱水ひまし油から選ばれた少なくとも1種
の分散剤0.5〜5重量部を含有する前記多孔性フィル
ム、前記樹脂組成物100重量部に対し、液状のエチレ
ン−α−オレフィンオリゴマー0.5〜5重量部を含有
する前記多孔性フィルム、及び、前記樹脂組成物100
重量部に対し、エチレンビスステアリン酸アミド及びメ
チレンビスステアリン酸アミドから選ばれた少なくとも
1種の滑剤0.5〜10重量部を含有する前記多孔性フ
ィルムが挙げられる。In a preferred embodiment of the porous film according to the present invention, 0.5 to 5 parts by weight of at least one dispersant selected from hardened castor oil and dehydrated castor oil is contained with respect to 100 parts by weight of the resin composition. The porous film, which contains 0.5 to 5 parts by weight of a liquid ethylene-α-olefin oligomer based on 100 parts by weight of the resin composition, and the resin composition 100
The porous film contains 0.5 to 10 parts by weight of at least one lubricant selected from ethylene bisstearic acid amide and methylene bisstearic acid amide with respect to parts by weight.
【0009】本発明に係わる多孔性フィルムは、少なく
とも18g/25mm/(g/m2)の機械方向の5%
伸び強度及び少なくとも27g/25mm/(g/
m2)の機械方向の10%伸び強度から選ばれた少なく
とも1種の特性を有し、且つ、機械方向の剛軟性が2.
7mm/(g/m2)以下、透湿度が1500g/m2・
24h以上、目付けが10〜35g/m2である。ま
た、機械方向の熱収縮率が3%以下であることがより好
ましい。The porous film according to the present invention has at least 5% of the machine direction of 18 g / 25 mm / (g / m 2 ).
Elongation strength and at least 27 g / 25 mm / (g /
m 2 ) having at least one property selected from a 10% elongation strength in the machine direction, and a rigidity in the machine direction of 2.
7 mm / (g / m 2 ) or less, moisture permeability 1500 g / m 2 ·
The basis weight is 10 to 35 g / m 2 for 24 hours or more. Further, the heat shrinkage in the machine direction is more preferably 3% or less.
【0010】上記特性を有する本発明に係わる多孔性フ
ィルムは、前記樹脂組成物をフィルム成形し、得られた
フィルムを少なくとも機械方向に1.5〜3倍延伸して
多孔性フィルムとなし、次いで、90〜120℃におい
て、機械方向の収縮率を10〜25%に制御しながら少
なくとも0.004分間熱固定することにより製造され
る。The porous film according to the present invention having the above properties is obtained by forming the resin composition into a film, stretching the obtained film at least 1.5 to 3 times in the machine direction to form a porous film, , 90-120 ° C, and heat-set for at least 0.004 minutes while controlling the shrinkage in the machine direction at 10-25%.
【0011】本発明の多孔性フィルムは、従来品と同レ
ベルの透湿度を有し、且つ、機械方向の低ひずみ伸び強
度に優れ、しかも柔軟性に富み、風合いが良好である。
そのため、使い捨ておむつ、衛生用パッド等の人肌に装
着して用いるサニタリー用品の資材として有用である。
特に、機械方向の低ひずみ伸び強度に優れることから、
上記サニタリー用品に印刷等を施す場合には、印刷のピ
ッチがずれることがなく、鮮明な図柄などが得られる。[0011] The porous film of the present invention has the same level of moisture permeability as conventional products, is excellent in low strain elongation in the machine direction, is rich in flexibility, and has good texture.
Therefore, it is useful as a material for sanitary articles worn on human skin such as disposable diapers and sanitary pads.
In particular, because of its excellent low strain elongation strength in the machine direction,
When performing printing or the like on the sanitary article, a clear pattern or the like can be obtained without shifting the printing pitch.
【0012】[0012]
【発明の実施の形態】以下、本発明について詳細に説明
する。本発明の多孔性フィルムは、ポリオレフィン系樹
脂及び無機充填材を含む多孔性フィルムを製造するに際
し、ポリオレフィン系樹脂として、(1)特定の密度の
高密度ポリエチレン及びポリプロピレンの少なくとも1
種、(2)特定の密度の線形低密度ポリエチレン、及
び、(3)分岐状低密度ポリエチレンの3種類の樹脂の
特定量を用い、これらに無機充填材を添加した樹脂組成
物をフィルム成形し、得られたフィルムを少なくとも機
械方向に延伸して多孔性フィルムとなし、次いで、熱固
定することにより製造される。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. When the porous film of the present invention is used to produce a porous film containing a polyolefin resin and an inorganic filler, at least one of (1) high-density polyethylene and polypropylene having a specific density is used as the polyolefin resin.
Using a specific amount of three types of resins, (2) linear low-density polyethylene having a specific density and (3) branched low-density polyethylene, and forming a resin composition in which an inorganic filler is added thereto, into a film. The film is produced by stretching the obtained film at least in the machine direction to form a porous film, and then heat-setting.
【0013】本発明に用いる高密度ポリエチレンは、エ
チレンの単独重合体であり、密度0.930〜0.97
0g/cm3のものである。市販品は、三井化学(株)
製、商品名:ハイゼックス3300F[密度:0.95
4g/cm3、メルトインデックス(以下、MIとい
う):1.1g/10min]、同ハイゼックス500
0SF[密度:0.959g/cm3、MI:0.65g
/10min]などが挙げられる。The high-density polyethylene used in the present invention is a homopolymer of ethylene and has a density of 0.930 to 0.97.
0 g / cm 3 . Commercial products are Mitsui Chemicals, Inc.
Product name: HIZEX 3300F [Density: 0.95
4 g / cm 3 , melt index (hereinafter referred to as MI): 1.1 g / 10 min], and Hyzex 500
0SF [density: 0.959 g / cm 3 , MI: 0.65 g
/ 10 min].
【0014】ポリプロピレンとしては、プロピレンの単
独重合体あるいはプロピレンと他のα−オレフィンとの
共重合体であり、密度0.900〜0.940g/cm
3で、MIが0.1〜30.0g/10minのもので
ある。市販のポリプロピレンとしては、グランドポリマ
ー(株)製、商品名:F103WH(密度:0.910
g/cm3、MI:2.4g/10min)などが挙げ
られる。The polypropylene is a homopolymer of propylene or a copolymer of propylene and another α-olefin, having a density of 0.900 to 0.940 g / cm
3 , MI is 0.1 to 30.0 g / 10 min. Commercially available polypropylene, manufactured by Grand Polymer Co., Ltd., trade name: F103WH (density: 0.910
g / cm 3 , MI: 2.4 g / 10 min).
【0015】本発明においては、上記高密度ポリエチレ
ン及びポリプロピレンの少なくとも1種の樹脂、即ち、
高密度ポリエチレン又はポリプロピレンを単独、あるい
は、両者の混合物が用いられる。高密度ポリエチレン及
びポリプロピレンの使用量は、得られる多孔性フィルム
の低ひずみ伸び強度、剛軟性、風合い等に影響を及ぼ
す。これらの使用量が多いと、剛軟性が増加し、手で触
るとガサガサ音がして風合いが悪くなる。逆に少ないと
低ひずみ伸び強度が低下する。かかる点を考慮すると、
高密度ポリエチレン及びポリプロピレンから選ばれた少
なくとも1種の樹脂の使用量は、ポリオレフィン系樹脂
の総量の10〜70重量%であることが好ましい。In the present invention, at least one resin of the above-mentioned high-density polyethylene and polypropylene, that is,
High-density polyethylene or polypropylene may be used alone or a mixture of both. The amount of the high-density polyethylene and polypropylene used affects the low strain elongation strength, stiffness, texture, and the like of the obtained porous film. If these amounts are large, the softness increases, and when touched by hand, a rough sound is made and the texture becomes poor. Conversely, if the amount is small, the low strain elongation strength decreases. With this in mind,
The amount of at least one resin selected from high-density polyethylene and polypropylene is preferably 10 to 70% by weight of the total amount of the polyolefin-based resin.
【0016】線形低密度ポリエチレンとしては、密度が
0.905〜0.930g/cm3、MIが0.1〜2
0.0g/10minであるものが用いられる。市販の
線形低密度ポリエチレンとしては、三井化学(株)製、
商品名:ウルトゼックスUZ2021L(密度:0.9
20g/cm3、MI:2.1g/10min)、エボ
リューSP2540(密度:0.925g/cm3、M
I:4.0g/10min)などがあげられる。線形低
密度ポリエチレンの使用量は、得られる多孔性フィルム
の強度、剛軟性に影響を及ぼす。使用量が多いと、強度
が低下する。逆に少ないと剛軟性が増加する。かかる点
を考慮すると、線形低密度ポリエチレンの使用量は、ポ
リオレフィン系樹脂の総量の88〜15重量%であるこ
とが好ましい。The linear low-density polyethylene has a density of 0.905 to 0.930 g / cm 3 and an MI of 0.1 to 2
What is 0.0g / 10min is used. Commercially available linear low-density polyethylene is available from Mitsui Chemicals, Inc.
Product name: Ultzex UZ2021L (density: 0.9
20 g / cm 3 , MI: 2.1 g / 10 min), Evolu SP2540 (density: 0.925 g / cm 3 , M
I: 4.0 g / 10 min). The amount of the linear low-density polyethylene used affects the strength and rigidity of the obtained porous film. If the amount is large, the strength is reduced. Conversely, if less, the flexibility increases. Considering this point, the amount of the linear low-density polyethylene is preferably 88 to 15% by weight of the total amount of the polyolefin-based resin.
【0017】分岐状低密度ポリエチレンとしては、密度
が0.910〜0.940g/cm 3、MIが0.1〜
20.0g/10minであるものが用いられる。市販
の分岐状低密度ポリエチレンとしては、三井化学(株)
製、商品名:ミラソンF967(密度:0.918g/
cm3、MI:1.0g/10min)、ミラソン10
2(密度:0.919g/cm3、MI:0.35g/
10min)などが挙げられる。分岐状低密度ポリエチ
レンの使用量は、得られる多孔性フィルムの厚みの均一
性に影響を及ぼす。使用量が少ないと厚みの均一性が悪
化する。かかる観点から、分岐状低密度ポリエチレンの
使用量は、ポリオレフィン系樹脂の総量の2〜15重量
%であることが好ましい。As the branched low-density polyethylene, density
Is 0.910 to 0.940 g / cm Three, MI is 0.1 ~
What is 20.0 g / 10min is used. Commercially available
Mitsui Chemicals, Inc.
Product name: Mirason F967 (density: 0.918 g /
cmThree, MI: 1.0 g / 10 min), Mirason 10
2 (density: 0.919 g / cmThree, MI: 0.35 g /
10 min). Branched low density polyethylene
The amount of ren used is the uniform thickness of the resulting porous film.
Affects gender. If the amount used is small, the thickness uniformity is poor
Become From such a viewpoint, the branched low-density polyethylene
The amount used is 2 to 15 weight of the total amount of the polyolefin resin.
%.
【0018】本発明に用いる上記ポリオレフィン系樹脂
は、ツィーグラー触媒の如きマルチサイト触媒を用いて
製造された樹脂であっても、また、メタロセン触媒の如
きシングルサイト触媒を用いて製造された樹脂であって
もよい。The polyolefin resin used in the present invention may be a resin produced using a multi-site catalyst such as a Ziegler catalyst or a resin produced using a single-site catalyst such as a metallocene catalyst. You may.
【0019】無機充填材は、例えば、炭酸カルシウム、
硫酸バリウム、硫酸カルシウム、炭酸バリウム、水酸化
マグネシウム、水酸化アルミニウム、酸化亜鉛、酸化マ
グネシウム、酸化チタン、シリカ、タルク等があげら
れ、これらのうち、炭酸カルシウム及び硫酸バリウムが
特に好ましい。無機充填材の平均粒径は20μm以下の
ものが好ましく、更に好ましくは10μm以下であり、
0.5〜5μmのものが最も好ましい。また、無機充填
材は、樹脂との分散性を向上させるために表面処理が施
されているものが、より好ましい。表面処理剤として
は、無機充填材の表面を被覆することにより、その表面
を疎水化できるものが好ましく、例えば、ステアリン
酸、ラウリン酸等の高級脂肪酸または、それらの金属塩
をあげることができる。The inorganic filler is, for example, calcium carbonate,
Examples thereof include barium sulfate, calcium sulfate, barium carbonate, magnesium hydroxide, aluminum hydroxide, zinc oxide, magnesium oxide, titanium oxide, silica, and talc. Of these, calcium carbonate and barium sulfate are particularly preferred. The average particle diameter of the inorganic filler is preferably 20 μm or less, more preferably 10 μm or less,
Most preferably, the thickness is 0.5 to 5 μm. Further, it is more preferable that the inorganic filler has been subjected to a surface treatment in order to improve the dispersibility with the resin. As the surface treatment agent, those capable of rendering the surface hydrophobic by coating the surface of the inorganic filler are preferable, and examples thereof include higher fatty acids such as stearic acid and lauric acid, and metal salts thereof.
【0020】前記ポリオレフィン系樹脂と無機充填材と
の組成比は、前記ポリオレフィン系樹脂が25〜55重
量%、無機充填材が75〜45重量%である。好ましく
は、ポリオレフィン系樹脂が30〜50重量%、無機充
填材が70〜50重量%の範囲である。無機充填材が4
5重量部未満になると、ポリオレフィン系樹脂と無機充
填材の界面が剥離してできる隣接したボイド同士が連通
しにくくなり、通気性が悪化する。また、75重量部を
超えると、フィルムの延伸時の伸びがなくなり、延伸が
困難になる。The composition ratio of the polyolefin resin to the inorganic filler is 25 to 55% by weight of the polyolefin resin and 75 to 45% by weight of the inorganic filler. Preferably, the content of the polyolefin resin is 30 to 50% by weight, and the content of the inorganic filler is 70 to 50% by weight. 4 inorganic fillers
When the amount is less than 5 parts by weight, adjacent voids formed by peeling off the interface between the polyolefin resin and the inorganic filler become difficult to communicate with each other, and the air permeability deteriorates. On the other hand, if it exceeds 75 parts by weight, elongation during stretching of the film is lost, and stretching becomes difficult.
【0021】本発明の多孔性フィルムは、上記樹脂組成
物から製造されたものであることに特徴がある。厚みの
均一性を向上する方法として、前記樹脂組成物100重
量部に対し、(1)硬化ひまし油、脱水ひまし油、又は
これらの混合物を0.5〜5重量部を添加する方法、
(2)液状のエチレン−α−オレフィンオリゴマーを
0.5〜5重量部添加する方法、および、(3)エチレ
ンビスステアリン酸アミド、メチレンビスステアリン酸
アミド、又はこれらの混合物を0.5〜10重量部含有
させる方法が有効である。上記(1)及び(2)の方法
は、多孔性フィルムの柔軟性を向上させる効果もある。The porous film of the present invention is characterized in that it is produced from the above resin composition. As a method for improving the uniformity of the thickness, a method of adding 0.5 to 5 parts by weight of (1) hardened castor oil, dehydrated castor oil, or a mixture thereof to 100 parts by weight of the resin composition;
(2) a method of adding 0.5 to 5 parts by weight of a liquid ethylene-α-olefin oligomer, and (3) a method of adding 0.5 to 10 parts of ethylenebisstearic acid amide, methylenebisstearic acid amide, or a mixture thereof. It is effective to include the parts by weight. The methods (1) and (2) also have the effect of improving the flexibility of the porous film.
【0022】ここで、硬化ひまし油とは、12−ヒドロ
キシオクタデカジエン酸を70重量%以上含む脂肪酸混
合物とグリセリンとのエステルである。市販品として、
伊藤製油(株)製、商品名:カスターワックスが挙げら
れる。脱水ひまし油とは、9,11−オクタデカジエン
酸30重量%以上、及び9,12−オクタデカジエン酸
30重量%以上、且つ、両酸を合計で70重量%以上含
む脂肪酸混合物とグリセリンとのエステルである。市販
品として、伊藤製油(株)製、商品名:DCOが挙げら
れる。Here, the hardened castor oil is an ester of a fatty acid mixture containing at least 70% by weight of 12-hydroxyoctadecadienoic acid and glycerin. As a commercial product,
Ito Oil Co., Ltd., trade name: Custer wax. Dehydrated castor oil is defined as a mixture of glycerin and a fatty acid mixture containing at least 30% by weight of 9,11-octadecadienoic acid, at least 30% by weight of 9,12-octadecadienoic acid, and at least 70% by weight of both acids in total. It is an ester. As a commercially available product, DCO manufactured by Ito Oil Co., Ltd. may be used.
【0023】また、液状のエチレン−α−オレフィンオ
リゴマーとは、エチレンとα−オレフィンを共重合させ
たもので、40℃での動粘度(JIS K2283)が
50〜100000mm2/sのものである。また、マ
レイン酸基などの極性基を導入し、酸で変性したエチレ
ン−α−オレフィン共重合体も好適に用いられる。市販
のエチレン−α−オレフィンオリゴマーとしては、ルー
カントHC600(三井化学(株)製、商品名)などが
挙げられる。The liquid ethylene-α-olefin oligomer is obtained by copolymerizing ethylene and α-olefin, and has a kinematic viscosity at 40 ° C. (JIS K2283) of 50 to 100000 mm 2 / s. . Further, an ethylene-α-olefin copolymer modified with an acid by introducing a polar group such as a maleic acid group is also preferably used. Commercially available ethylene-α-olefin oligomers include Lucant HC600 (trade name, manufactured by Mitsui Chemicals, Inc.).
【0024】また、他にも、通常の樹脂組成物に用いら
れている添加物を配合してもよい。このような添加物と
しては、例えば、酸化防止剤、熱安定剤、光安定剤、紫
外線吸収剤、中和剤、滑剤、防曇剤、アンチブロッキン
グ剤、帯電防止剤、スリップ剤、着色剤等が挙げられ
る。Further, other additives used in ordinary resin compositions may be blended. Such additives include, for example, antioxidants, heat stabilizers, light stabilizers, ultraviolet absorbers, neutralizers, lubricants, antifoggants, antiblocking agents, antistatic agents, slip agents, colorants, and the like. Is mentioned.
【0025】本発明の多孔性フィルムは次の方法で製造
される。ポリオレフィン系樹脂と無機充填材、必要に応
じて他の添加剤とを混合した後、ヘンシェルミキサー、
スーパーミキサー、タンブラー型等の混合機を用いて混
合し、その後、通常の一軸あるいは二軸スクリュー押出
機、タンデム型混練押出機によって混練し、ペレット化
する。次いで、そのペレットをポリオレフィン樹脂の融
点以上、好ましくは融点+20℃以上、分解温度未満の
温度において、Tダイ等が装着された押出成形機、円形
ダイが装着されたインフレーション成形機等の公知の成
形機を用いて溶融、製膜する。場合によっては、ペレッ
ト化せず、直接成形機で製膜することもできる。The porous film of the present invention is produced by the following method. After mixing the polyolefin resin and the inorganic filler, and other additives as necessary, a Henschel mixer,
The mixture is mixed using a mixer such as a super mixer or a tumbler type, and then kneaded by a usual single-screw or twin-screw extruder or a tandem-type kneading extruder to form pellets. Next, the pellets are molded at a temperature equal to or higher than the melting point of the polyolefin resin, preferably equal to or higher than the melting point + 20 ° C. and lower than the decomposition temperature, by a known molding method such as an extruder equipped with a T-die or the like or an inflation molding machine equipped with a circular die. Melting and film formation using a machine. In some cases, it is also possible to form a film directly with a molding machine without pelletizing.
【0026】製膜されたフィルムは、公知のロール法、
テンター法、ギアストレッチ法などの延伸法により、1
0℃以上、樹脂の軟化点(JIS K−6760に規定
される方法により測定した値)未満の温度範囲において
延伸する。それぞれの方法において、延伸倍率を変える
ことにより、透湿度をコントロールする。延伸方向は、
少なくとも機械方向(以下、MD方向という)を含む方
向に延伸する。MD方向、及びMD方向と直交する方向
(以下、TD方向)に2軸延伸してもよい。その場合、
1段で行ってもよいし、多段階に分けておこなってもよ
い。延伸倍率は、1.5〜3倍程度である。延伸倍率が
1.5倍未満では、充分な透湿度が得られない。3倍を
超えると、熱収縮率が悪くなる傾向がある。The formed film is formed by a known roll method,
By stretching method such as tenter method and gear stretching method, 1
The film is stretched in a temperature range of 0 ° C. or higher and lower than the softening point of the resin (a value measured by a method specified in JIS K-6760). In each method, the moisture permeability is controlled by changing the stretching ratio. The stretching direction is
The film is stretched in a direction including at least the machine direction (hereinafter, referred to as the MD direction). Biaxial stretching may be performed in the MD direction and a direction perpendicular to the MD direction (hereinafter, TD direction). In that case,
It may be performed in one stage or may be performed in multiple stages. The stretching ratio is about 1.5 to 3 times. If the stretching ratio is less than 1.5 times, sufficient moisture permeability cannot be obtained. If it exceeds three times, the heat shrinkage tends to be poor.
【0027】フィルムの熱収縮率を抑える方法として
は、延伸後のフィルムを、熱固定する方法が挙げられ
る。ここで、熱固定とは、延伸工程の後、あらかじめフ
ィルムに熱をかけ、フィルムをわざと収縮させて、でき
たフィルムの収縮を抑えることをいう。熱固定の方法と
しては、延伸後のフィルムを、熱をかけたロール(アニ
ールロール)により加熱する方法が挙げられる。温度が
低すぎると、フィルムの熱収縮率が大きくなり、温度が
高すぎると、フィルムがロールに引っ付き巻きつくトラ
ブルが起こる。かかる点を考慮すると、熱固定温度は9
0〜120℃が好ましい。As a method of suppressing the heat shrinkage of the film, there is a method of heat setting the stretched film. Here, the heat setting means that after the stretching step, heat is applied to the film in advance to shrink the film intentionally, thereby suppressing the shrinkage of the formed film. As a method of heat setting, a method in which the stretched film is heated by a roll to which heat is applied (annealing roll) is used. If the temperature is too low, the heat shrinkage of the film increases, and if the temperature is too high, there occurs a problem that the film is caught on a roll and wound around. Considering this point, the heat setting temperature is 9
0-120 ° C is preferred.
【0028】熱固定の時間は、フィルムがアニールロー
ルと接している時間をいう。アニールロールの本数は1
本でも、2本以上でも良く、2本以上の場合の熱固定時
間は、各ロールにフィルムが接する時間の和である。熱
固定時間は、0.004分以上でないと熱固定が不充分
となり、耐熱収縮率が悪化する。熱固定時間の上限は、
アニールロールの温度(熱固定温度)により変わるが、
上記温度範囲であれば1時間程度で十分である。また、
熱固定の際、フイルムのアニール率(収縮率)は、アニ
ールロールと、それに続くロール(冷却ロール)との速
度差により決められるが、10〜25%が好ましい。ア
ニール率は{1−(冷却ロール速度/アニールロール速
度)}×100で表すことができる。アニール率が小さ
すぎると、フィルムの熱収縮率が大きくなり、アニール
率が大きすぎると、製造時にフィルムがたるんで、安定
して生産ができなくなる。アニールロールはフィルムに
効率良く熱を伝えるため、金属製であることが望まし
い。The heat setting time refers to the time during which the film is in contact with the annealing roll. Number of annealing rolls is 1
The number of books may be two or more, and in the case of two or more, the heat setting time is the sum of the time when the film is in contact with each roll. If the heat setting time is not more than 0.004 minutes, the heat setting becomes insufficient, and the heat shrinkage rate deteriorates. The upper limit of the heat setting time is
It depends on the temperature of the annealing roll (heat setting temperature),
About one hour is sufficient in the above temperature range. Also,
At the time of heat setting, the annealing rate (shrinkage rate) of the film is determined by the speed difference between the annealing roll and the subsequent roll (cooling roll), but is preferably 10 to 25%. The annealing rate can be represented by {1- (cooling roll speed / annealing roll speed)} × 100. If the annealing rate is too low, the heat shrinkage of the film will increase, and if the annealing rate is too high, the film will sag during production and production will not be stable. The annealing roll is desirably made of metal to efficiently transmit heat to the film.
【0029】本発明の多孔性フィルムは、上記のように
して製造されるが、主たる特性は、少なくとも18g/
25mm/(g/m2)の機械方向の5%伸び強度及び
少なくとも27g/25mm/(g/m2)の機械方向
の10%伸び強度から選ばれた少なくとも1種の特性を
有し、且つ、機械方向の剛軟性が2.7mm/(g/m
2)以下、透湿度が1500g/m2・24h以上、目付
けが10〜35g/m 2である。また、機械方向の熱収
縮率が3%以下であることがより好ましい。[0029] The porous film of the present invention can be used as described above.
The main properties are at least 18 g /
25 mm / (g / mTwo) 5% elongation strength in the machine direction and
At least 27 g / 25 mm / (g / mTwo) Machine direction
At least one property selected from 10% elongation strength
And the rigidity in the machine direction is 2.7 mm / (g / m
Two) Below, the moisture permeability is 1500 g / mTwo・ Above 24h
Injury 10 to 35 g / m TwoIt is. Also, heat collection in the machine direction
More preferably, the shrinkage ratio is 3% or less.
【0030】上記のように、本発明の多孔性フィルムの
機械方向の5%伸び強度、及び/又は、機械方向の10
%伸び強度が上記値であるので、印刷等を施す場合に
は、印刷のピッチがずれることがなく、鮮明な図柄など
が得られる。また、機械方向の剛軟性が上記値であるの
で、手などで触った際にガサガサした音がせず、風合い
が良好である。As described above, the porous film of the present invention has a 5% elongation strength in the machine direction and / or a 10% elongation strength in the machine direction.
Since the% elongation strength is the above value, when performing printing or the like, a clear pattern or the like can be obtained without deviation of the printing pitch. In addition, since the rigidity in the machine direction is the above value, a rough sound is not generated when touched with a hand or the like, and the texture is good.
【0031】実施例 以下、本発明について更に具体的に説明するため、以下
に実施例を示す。尚、本発明はこれらの実施例に限定さ
れるものではない。実施例に示した透湿度、剛軟性、強
度、伸びは下記方法により測定した値である。EXAMPLES Examples will be given below to describe the present invention more specifically. Note that the present invention is not limited to these examples. The moisture permeability, stiffness, strength and elongation shown in the examples are values measured by the following methods.
【0032】(1)透湿度(g/m2・24hr) 多孔性フイルムから試料(10cm×10cm)を10
枚採取し、ASTME−96に規定される方法に準拠し
て、温度40℃、相対湿度60%、純水法の条件で測定
し、その平均値を算出する。測定時間は24時間とす
る。測定初期の水面と試料の距離は8mmとする。(1) Moisture Permeability (g / m 2 · 24 hr) A sample (10 cm × 10 cm) was taken from a porous film.
Samples are taken and measured under the conditions of a temperature of 40 ° C., a relative humidity of 60% and a pure water method in accordance with the method specified in ASTME-96, and the average value is calculated. The measurement time is 24 hours. The distance between the water surface and the sample at the beginning of the measurement is 8 mm.
【0033】(2)機械方向の剛軟性(mm) JIS−L1096に規定される方法(カンチレバー
法)に準拠して測定する。<試料の調製>幅200m
m、長さ(MD方向)300mm、目付け20g/m2
の多孔性フィルムを幅25mmの金尺に巻きつけた後,
金尺を抜き取る。得られた偏平状の巻物(幅25mm、
長さ300mm)を重量1kgのローラーにより、1往
復押圧して試料とする。(2) Stiffness in machine direction (mm) Measured according to the method (cantilever method) specified in JIS-L1096. <Preparation of sample> 200m width
m, length (MD direction) 300 mm, basis weight 20 g / m 2
After wrapping a porous film of
Pull out the gold scale. The obtained flat scroll (width 25 mm,
(Length: 300 mm) is pressed back and forth once by a roller weighing 1 kg to obtain a sample.
【0034】(3)低ひずみ伸び強度[g/25mm/
(g/m2)] 目付け20g/m2の多孔性フィルムから、巾25m
m、長さ(MD方向)150mmのサンプルを切り取
る。ASTM D882に従い、チャック間距離50m
m、引張り速度500mm/minでMD方向に引張
り、サンプル(チャック間距離)が、5%(2.5m
m)、10%(5mm)伸びたときのMD方向の強度
(応力)を測定する。(3) Low strain elongation strength [g / 25 mm /
(G / m 2 )] From a porous film with a basis weight of 20 g / m 2 , a width of 25 m
Cut out a sample with a length of 150 mm in the MD direction (MD direction). According to ASTM D882, distance between chucks 50m
m, pulling in the MD direction at a pulling speed of 500 mm / min.
m) The strength (stress) in the MD direction when stretched by 10% (5 mm) is measured.
【0035】(4)機械方向の熱収縮率(%) 多孔性フイルムから試料(MD:20cm、TD:1c
m)を10枚採取し、MD方向に標線間が10cmにな
るよう標線を入れる。温度60℃の条件に1時間放置
し、室温に冷却後、標線間を鋼尺で測定する。下記数式
(1)により算出する。 S={(N0−N1)/N0}×100・・(1) ここで、S:収縮率,N0:加熱前の標線間距離、N1:
加熱後の標線間距離。(4) Heat shrinkage (%) in the machine direction Sample (MD: 20 cm, TD: 1c)
m) are sampled, and marked lines are inserted in the MD direction so that the distance between the marked lines is 10 cm. After leaving for 1 hour at a temperature of 60 ° C. and cooling to room temperature, the distance between the marked lines is measured with a steel measure. It is calculated by the following equation (1). S = {(N 0 −N 1 ) / N 0 } × 100 (1) where S: shrinkage, N 0 : distance between marked lines before heating, N 1 :
Marked distance after heating.
【0036】(5)厚み均一性 目付け20g/m2の多孔性フィルムから試料[機械方
向:21cm、機械方向と直角方向:5cm]を3枚採
取し、縦方向に1cm間隔で合計60箇所の測定点につ
いて、厚み測定機(PEACOCK社製、UPRIGH
T DIALGAUGE NO.25)を用いて厚みを
測定し、平均厚み(X)、最高厚み(MAX)及び最低
厚み(MIN)を求め、[(MAX)−(MIN)]/
(X)を算出して、これをフィルム厚みの均一性とす
る。(5) Thickness uniformity Three samples (machine direction: 21 cm, direction perpendicular to the machine direction: 5 cm) were collected from a porous film having a basis weight of 20 g / m 2 , and a total of 60 samples were taken at 1 cm intervals in the vertical direction. Regarding the measurement points, use a thickness measuring device (UPACHI, manufactured by PEACOCK).
T DIALGAUGE NO. 25), the average thickness (X), the maximum thickness (MAX), and the minimum thickness (MIN) are determined, and [(MAX) − (MIN)] /
Calculate (X) and use this as the uniformity of the film thickness.
【0037】(6)カサカサ音 フィルムを折り曲げた際の感触を示す。◎:ほとんどカ
サカサ音がしない。○:わずかにカサカサ音がする。
△:カサカサ音がする。×:カサカサ音がひどい。(6) Crispy sound The feeling when the film is bent. :: There is almost no rustling sound. :: There is a slight rustling sound.
Δ: A rustling sound is heard. ×: The rustling sound is severe.
【0038】(7)総合評価 ○:透湿度が1500g/m2・24hr以上、5%伸
び強度が18g/25mm/(g/m2)以上、及び/
又は10%伸び強度が27g/25mm/(g/m2)
以上、機械方向の剛軟性が2.7mm/(g/m2)以
下のもの。×:これらの特性が上記以外のもの。(7) Comprehensive evaluation :: Water vapor permeability of 1500 g / m 2 · 24 hr or more, 5% elongation strength of 18 g / 25 mm / (g / m 2 ) or more, and / or
Or, the 10% elongation strength is 27 g / 25 mm / (g / m 2 )
As described above, the rigidity in the machine direction is 2.7 mm / (g / m 2 ) or less. X: These characteristics are other than the above.
【0039】実施例1 高密度ポリエチレン(三井化学(株)製、商品名:ハイ
ゼックス3300F、密度:0.954g/cm3、M
I:1.1g/10min)13重量部(ポリオレフィ
ン系樹脂中32.5重量%)、線形低密度ポリエチレン
(三井化学(株)製、商品名:エボリューSP254
0、密度:0.925g/cm3、MI:4.0g/1
0min)25重量部(ポリオレフィン系樹脂中62.
5%)、分岐状低密度ポリエチレン(三井化学(株)
製、商品名:ミラソンF967、密度:0.918g/
cm3、MI:1.0g/10min)2重量部(ポリ
オレフィン系樹脂中5%)、炭酸カルシウム(同和カル
ファイン(株)製、商品名:SST−40)60重量部
をタンブラーミキサーにて混合した後、タンデム型混練
押出機を用いて、230℃において均一に混練し、ペレ
ット状に加工した。このペレットをTダイが装着された
押出成形機を用いて、240℃において溶融製膜し、7
0℃に加熱した予熱ロールと延伸ロールとの間で、2.
0倍の延伸倍率で、ライン速度20m/minで機械方
向に一軸延伸し、引き続き、熱固定用ロール(直径30
cm)2本を用い(熱固定時間0.047分)、85
℃、アニール率8%で熱固定を行い、目付け20g/m
2の多孔性フィルムを得た。樹脂組成物の組成及びアニ
ール条件を表1、得られた結果を表2に示す。Example 1 High-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: HIZEX 3300F, density: 0.954 g / cm 3 , M
I: 1.1 g / 10 min) 13 parts by weight (32.5% by weight in polyolefin resin), linear low density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Evolue SP254)
0, density: 0.925 g / cm 3 , MI: 4.0 g / 1
0 min) 25 parts by weight (62.
5%), branched low-density polyethylene (Mitsui Chemicals, Inc.)
Product name: Mirason F967, density: 0.918 g /
cm 3 , MI: 1.0 g / 10 min) 2 parts by weight (5% in polyolefin resin) and 60 parts by weight of calcium carbonate (trade name: SST-40, manufactured by Dowa Calfine Co., Ltd.) using a tumbler mixer. After that, the mixture was uniformly kneaded at 230 ° C. using a tandem-type kneading extruder, and processed into pellets. The pellets were melt-formed at 240 ° C. by using an extruder equipped with a T-die.
1. between a preheated roll heated to 0 ° C. and a stretch roll;
The film is uniaxially stretched in the machine direction at a stretch ratio of 0 at a line speed of 20 m / min, and subsequently, a heat fixing roll (diameter 30)
cm) using two pieces (heat fixing time: 0.047 minutes), 85
Thermal fixation at 8 ° C and an annealing rate of 8%.
2 porous films were obtained. Table 1 shows the composition of the resin composition and annealing conditions, and Table 2 shows the obtained results.
【0040】実施例2 実施例1の高密度ポリエチレンを、ポリプロピレン(グ
ランドポリマー(株)製、商品名:F103WH、密
度:0.910g/cm3、MI:2.4g/10mi
n)に変えた以外は、実施例1と同じ方法で多孔性フィ
ルムを得た。樹脂組成物の組成及びアニール条件を表
1、得られた結果を表2に示す。Example 2 The high-density polyethylene of Example 1 was replaced with polypropylene (manufactured by Grand Polymer Co., Ltd., trade name: F103WH, density: 0.910 g / cm 3 , MI: 2.4 g / 10 mi).
A porous film was obtained in the same manner as in Example 1 except that n) was changed. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0041】実施例3 実施例1のポリオレフィン系樹脂を、ポリプロピレン
(グランドポリマー(株)製、商品名:F103WH、
密度:0.910g/cm3、MI:2.4g/10m
in)18重量部(ポリオレフィン系樹脂中45%)、
線形低密度ポリエチレン(三井化学(株)製、商品名:
エボリューSP2540、密度:0.925g/c
m3、MI:4.0g/10min)20重量部(ポリ
オレフィン系樹脂中50%)、分岐状低密度ポリエチレ
ン(三井化学(株)製、商品名:ミラソンF967、密
度:0.918g/cm3、MI:1.0g/10mi
n)2重量部(ポリオレフィン系樹脂中5%)とし、ポ
リオレフィン系樹脂と炭酸カルシウムからなる組成物1
00重量部に対し、硬化ひまし油2重量部、脱水ひまし
油1重量部を加えた以外は、実施例1と同じ方法で多孔
性フィルムを得た。樹脂組成物の組成及びアニール条件
を表1、得られた結果を表2に示す。Example 3 The polyolefin resin of Example 1 was replaced with polypropylene (trade name: F103WH, manufactured by Grand Polymer Co., Ltd.).
Density: 0.910 g / cm 3 , MI: 2.4 g / 10 m
in) 18 parts by weight (45% in polyolefin resin),
Linear low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name:
Evolu SP2540, density: 0.925 g / c
m 3 , MI: 4.0 g / 10 min) 20 parts by weight (50% in polyolefin resin), branched low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Mirason F967, density: 0.918 g / cm 3) , MI: 1.0 g / 10 mi
n) 2 parts by weight (5% in polyolefin resin), composition 1 comprising polyolefin resin and calcium carbonate
A porous film was obtained in the same manner as in Example 1, except that 2 parts by weight of hardened castor oil and 1 part by weight of dehydrated castor oil were added to 00 parts by weight. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0042】実施例4 実施例3の硬化ひまし油(伊藤製油(株)製、商品名;
カスターワックス)2重量部、脱水ひまし油(伊藤製油
(株)製、商品名;DCO)1重量部から、脱水ひまし
油を除いた以外は、実施例3と同じ方法で多孔性フィル
ムを得た。樹脂組成物の組成及びアニール条件を表1、
得られた結果を表2に示す。Example 4 The hardened castor oil of Example 3 (trade name, manufactured by Ito Oil Co., Ltd.)
A porous film was obtained in the same manner as in Example 3, except that dehydrated castor oil was removed from 2 parts by weight of caster wax and 1 part by weight of dehydrated castor oil (trade name: DCO, manufactured by Ito Oil Co., Ltd.). Table 1 shows the composition of the resin composition and the annealing conditions.
Table 2 shows the obtained results.
【0043】実施例5 実施例3の硬化ひまし油(伊藤製油(株)製、商品名;
カスターワックス)2重量部、脱水ひまし油(伊藤製油
(株)製、商品名;DCO)1重量部を、ルーカントH
C600(三井化学(株)製)1重量部に変えた以外
は、実施例3と同じ方法で多孔性フィルムを得た。樹脂
組成物の組成及びアニール条件を表1、得られた結果を
表2に示す。Example 5 The hardened castor oil of Example 3 (trade name, manufactured by Ito Oil Co., Ltd.)
2 parts by weight of caster wax) and 1 part by weight of dehydrated castor oil (trade name: DCO, manufactured by Ito Oil Co., Ltd.)
A porous film was obtained in the same manner as in Example 3, except that 1 part by weight of C600 (manufactured by Mitsui Chemicals, Inc.) was used. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0044】実施例6 実施例3の硬化ひまし油(伊藤製油(株)製、商品名;
カスターワックス)2重量部、脱水ひまし油(伊藤製油
(株)製、商品名;DCO)1重量部を、エチレンビス
ステアリン酸アミド(日本化成(株)製、商品名:エチ
レンビスステアリン酸アマイド スリバックスE)2重
量部に変えた以外は、実施例3と同じ方法で多孔性フィ
ルムを得た。樹脂組成物の組成及びアニール条件を表
1、得られた結果を表2に示す。Example 6 The hardened castor oil of Example 3 (trade name, manufactured by Ito Oil Co., Ltd.)
2 parts by weight of caster wax) and 1 part by weight of dehydrated castor oil (trade name: DCO, manufactured by Ito Oil Co., Ltd.) were mixed with ethylene bisstearic acid amide (trade name, manufactured by Nippon Kasei Co., Ltd., trade name: ethylene bisstearic acid amide Srivac) E) A porous film was obtained in the same manner as in Example 3 except that the amount was changed to 2 parts by weight. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0045】実施例7 実施例3のポリオレフィン系樹脂を、高密度ポリエチレ
ン(三井化学(株)製、商品名:ハイゼックス3300
F)8重量部(ポリオレフィン系樹脂中20重量%、ポ
リプロピレン(グランドポリマー(株)製、商品名:F
103WH、密度:0.910g/cm3、MI:2.
4g/10min)9重量部(ポリオレフィン系樹脂中
22.5%)、線形低密度ポリエチレン(三井化学
(株)製、商品名:エボリューSP2540、密度:
0.925g/cm3、MI:4.0g/10min)
21重量部(ポリオレフィン系樹脂中52.5%)、分
岐状低密度ポリエチレン(三井化学(株)製、商品名:
ミラソンF967、密度:0.918g/cm3、M
I:1.0g/10min)2重量部(ポリオレフィン
系樹脂中5%)とした以外は実施例3と同じ方法で多孔
性フィルムを得た。樹脂組成物の組成及びアニール条件
を表1、得られた結果を表2に示す。Example 7 The polyolefin resin of Example 3 was replaced with a high-density polyethylene (trade name: HIZEX 3300, manufactured by Mitsui Chemicals, Inc.).
F) 8 parts by weight (20% by weight in polyolefin resin, polypropylene (manufactured by Grand Polymer Co., Ltd., trade name: F
103 WH, density: 0.910 g / cm 3 , MI: 2.
4 g / 10 min) 9 parts by weight (22.5% in polyolefin resin), linear low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Evolue SP2540, density:
0.925 g / cm 3 , MI: 4.0 g / 10 min)
21 parts by weight (52.5% in polyolefin resin), branched low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name:
Mirason F967, density: 0.918 g / cm 3 , M
I: 1.0 g / 10 min) A porous film was obtained in the same manner as in Example 3, except that 2 parts by weight (5% in polyolefin resin) was used. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0046】実施例8 実施例3のアニールの条件を、熱固定用ロール(直径3
0cm)2本を用い(熱固定時間0.047分)、10
5℃、アニール率15%で熱固定を行ったことに変えた
以外は、実施例3と同じ方法で多孔性フィルムを得た。
樹脂組成物の組成及びアニール条件を表1、得られた結
果を表2に示す。Example 8 The annealing conditions in Example 3 were changed to a heat fixing roll (diameter 3).
0cm) using two (heat fixation time 0.047 minutes), 10
A porous film was obtained in the same manner as in Example 3, except that the heat setting was performed at 5 ° C. and an annealing rate of 15%.
Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0047】比較例1 実施例1のポリオレフィン系樹脂を、ポリプロピレン
(グランドポリマー(株)製、商品名:F103WH、
密度:0.910g/cm3、MI:2.4g/10m
in)40重量部(ポリオレフィン系樹脂中100%)
とした以外は、実施例1と同じ方法で多孔性フィルムを
得た。樹脂組成物の組成及びアニール条件を表1、得ら
れた結果を表2に示す。Comparative Example 1 The polyolefin resin of Example 1 was replaced with polypropylene (manufactured by Grand Polymer Co., Ltd., trade name: F103WH).
Density: 0.910 g / cm 3 , MI: 2.4 g / 10 m
in) 40 parts by weight (100% in polyolefin resin)
A porous film was obtained in the same manner as in Example 1, except that Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0048】比較例2 実施例1のポリオレフィン系樹脂を、高密度ポリエチレ
ン(三井化学(株)製、商品名:ハイゼックス3300
F、密度:0.954g/cm3、MI:1.1g/1
0min)40重量部(ポリオレフィン系樹脂中100
%)とした以外は、実施例1と同じ方法で多孔性フィル
ムを得た。樹脂組成物の組成及びアニール条件を表1、
得られた結果を表2に示す。Comparative Example 2 The polyolefin resin of Example 1 was replaced with a high-density polyethylene (trade name: HIZEX 3300, manufactured by Mitsui Chemicals, Inc.).
F, density: 0.954 g / cm 3 , MI: 1.1 g / 1
0 min) 40 parts by weight (100 in polyolefin resin)
%), Except that the porous film was obtained in the same manner as in Example 1. Table 1 shows the composition of the resin composition and the annealing conditions.
Table 2 shows the obtained results.
【0049】比較例3 実施例1のポリオレフィン系樹脂を、ポリプロピレン
(グランドポリマー(株)製、商品名:F103WH、
密度:0.910g/cm3、MI:2.4g/10m
in)33重量部(ポリオレフィン系樹脂中82.5
%)、線形低密度ポリエチレン(三井化学(株)製、商
品名:エボリューSP2540、密度:0.925g/
cm3、MI:4.0g/10min)5重量部(ポリ
オレフィン系樹脂中12.5%)、分岐状低密度ポリエ
チレン(三井化学(株)製、商品名:ミラソンF96
7、)2重量部(ポリオレフィン系樹脂中5%)とした
以外は、実施例1と同じ方法で多孔性フィルムを得た。
樹脂組成物の組成及びアニール条件を表1、得られた結
果を表2に示す。Comparative Example 3 The polyolefin resin of Example 1 was replaced with polypropylene (manufactured by Grand Polymer Co., Ltd., trade name: F103WH,
Density: 0.910 g / cm 3 , MI: 2.4 g / 10 m
in) 33 parts by weight (82.5 in polyolefin resin)
%), Linear low density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Evolue SP2540, density: 0.925 g /
cm 3 , MI: 4.0 g / 10 min), 5 parts by weight (12.5% in polyolefin resin), branched low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Mirason F96)
7,) A porous film was obtained in the same manner as in Example 1, except that 2 parts by weight (5% in the polyolefin resin) was used.
Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0050】比較例4 実施例1のポリオレフィン系樹脂を、線形低密度ポリエ
チレン(三井化学(株)製、商品名:エボリューSP2
540、密度:0.925g/cm3、MI:4.0g
/10min)40重量部(ポリオレフィン系樹脂中1
00%)とし、硬化ひまし油(伊藤製油(株)製、商品
名;カスターワックス)2重量部、脱水ひまし油(伊藤
製油(株)製、商品名;DCO)1重量部を加えた以外
は、実施例1と同じ方法で多孔性フィルムを得た。樹脂
組成物の組成及びアニール条件を表1、得られた結果を
表2に示す。Comparative Example 4 The polyolefin resin of Example 1 was replaced with a linear low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Evolu SP2)
540, density: 0.925 g / cm 3 , MI: 4.0 g
/ 10 min) 40 parts by weight (1 in polyolefin resin)
00%) and 2 parts by weight of hardened castor oil (manufactured by Ito Oil Co., Ltd .; trade name: Custer Wax) and 1 part by weight of dehydrated castor oil (manufactured by Ito Oil Co., Ltd., trade name: DCO) were added. A porous film was obtained in the same manner as in Example 1. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0051】比較例5 実施例1のポリオレフィン系樹脂を、線形低密度ポリエ
チレン(三井化学(株)製、商品名:エボリューSP2
540、密度:0.925g/cm3、MI:4.0g
/10min)38重量部(ポリオレフィン系樹脂中9
5%)、分岐状低密度ポリエチレン(三井化学(株)
製、商品名:ミラソンF967、密度:0.918g/
cm3、MI:1.0g/10min)2重量部(ポリ
オレフィン系樹脂中5%)とし、硬化ひまし油(伊藤製
油(株)製、商品名;カスターワックス)2重量部、脱
水ひまし油(伊藤製油(株)製、商品名;DCO)1重
量部を加えた以外は、実施例1と同じ方法で多孔性フィ
ルムを得た。樹脂組成物の組成及びアニール条件を表
1、得られた結果を表2に示す。Comparative Example 5 The polyolefin resin of Example 1 was replaced with a linear low-density polyethylene (trade name: EVOLUE SP2 manufactured by Mitsui Chemicals, Inc.)
540, density: 0.925 g / cm 3 , MI: 4.0 g
/ 10 min) 38 parts by weight (9 in polyolefin resin)
5%), branched low-density polyethylene (Mitsui Chemicals, Inc.)
Product name: Mirason F967, density: 0.918 g /
cm 3 , MI: 1.0 g / 10 min) 2 parts by weight (5% in polyolefin resin), 2 parts by weight of hardened castor oil (trade name: Castor wax, manufactured by Ito Oil Co., Ltd.), and dehydrated castor oil (Ito Oil ( A porous film was obtained in the same manner as in Example 1 except that 1 part by weight of DCO) was added. Table 1 shows the composition of the resin composition and the annealing conditions, and Table 2 shows the obtained results.
【0052】[0052]
【表1】 [Table 1]
【0053】<表1の記号の説明> A:高密度ポリエチレン(三井化学(株)製、商品名:
ハイセ゛ックス3300F)、B:ポリプロピレン(グランドポリマ
ー(株)製、商品名:F103WH)、C:線形低密度
ポリエチレン(三井化学(株)製、商品名:エボリュー
SP2540)、D:線形低密度ポリエチレン(三井化
学(株)製、商品名:ウルトゼックス2021L)、
E:分岐状低密度ポリエチレン(三井化学(株)製、商
品名:ミラソンF967)、F:硬化ひまし油(伊藤製
油(株)製、商品名;カスターワックス)、G:脱水ひ
まし油(伊藤製油(株)製、商品名;DCO)、H:エ
チレン−α−オレフィンオリゴマー(三井化学(株)
製、商品名;ルーカントHC600)、I:エチレンビ
スステアリン酸アミド(日本化成(株)製、商品名:エ
チレンビスステアリン酸アマイド スリバックスE)、
J:炭酸カルシウム(同和カルファイン(株)製、商品
名:SST−40)<Description of Symbols in Table 1> A: High-density polyethylene (trade name, manufactured by Mitsui Chemicals, Inc.)
HiSex 3300F), B: polypropylene (Grand Polymer Co., Ltd., trade name: F103WH), C: linear low density polyethylene (Mitsui Chemicals, trade name: Evolu SP2540), D: linear low density polyethylene (Mitsui) Chemical Co., Ltd., trade name: Ultzex 2021L),
E: branched low-density polyethylene (manufactured by Mitsui Chemicals, Inc., trade name: Mirason F967), F: hardened castor oil (manufactured by Ito Oil Co., Ltd., trade name: caster wax), G: dehydrated castor oil (Ito Oil Co., Ltd.) ), Trade name: DCO), H: ethylene-α-olefin oligomer (Mitsui Chemicals, Inc.)
Manufactured by Nippon Kasei Co., Ltd., trade name: ethylene bisstearic acid amide Srivac E)
J: calcium carbonate (manufactured by Dowa Calfine Co., Ltd., trade name: SST-40)
【0054】[0054]
【表2】 [Table 2]
【0055】<実施例の考察>実施例1〜8で得られた
多孔性フィルムは、透湿度が高く、且つ、機械方向の低
ひずみ伸び強度に優れ、しかも柔軟性に富み、風合いが
良好である。厚みの均一性も良好である。一方、比較例
1と2で得られた多孔性フィルムは、低密度ポリエチレ
ンが含まれていないため、風合い(剛軟度、カサカサ
音)が悪い。また、分岐低密度ポリエチレンが含まれて
いないため、厚みの均一性も良くない。比較例3では、
低密度ポリエチレンが少ないため、比較例1,2よりは
改善されているが、風合いが悪い。比較例4では、HD
PE及びPPが含まれていないため、低ひずみ伸び強度
が低い。また、分岐低密度ポリエチレンが含まれていな
いため、厚み均一性も良くない。比較例5では、HDP
E及びPPが含まれていないため、低倍率伸び強度が低
い。<Consideration of Examples> The porous films obtained in Examples 1 to 8 have high moisture permeability, are excellent in low strain elongation strength in the machine direction, and have high flexibility and good texture. is there. The thickness uniformity is also good. On the other hand, since the porous films obtained in Comparative Examples 1 and 2 do not contain low-density polyethylene, they have poor texture (bending softness and rustling). In addition, since no branched low-density polyethylene is contained, the uniformity of the thickness is not good. In Comparative Example 3,
Since the amount of low-density polyethylene is small, it is better than Comparative Examples 1 and 2, but the texture is poor. In Comparative Example 4, the HD
Since it does not contain PE and PP, the low strain elongation strength is low. Further, the thickness uniformity is not good because no branched low-density polyethylene is contained. In Comparative Example 5, HDP
Since E and PP are not contained, the low-magnification elongation strength is low.
【0056】[0056]
【発明の効果】本発明の多孔性フィルムは、従来品と同
レベルの透湿度を有し、且つ、機械方向の低ひずみ伸び
強度に優れ、しかも柔軟性に富み、風合いが良好であ
る。そのため、使い捨ておむつ、衛生用パッド等の人肌
に装着して用いるサニタリー用品の資材として有用であ
る。特に、機械方向の低ひずみ伸び強度に優れることか
ら、上記サニタリー用品に印刷等を施す場合には、印刷
のピッチがずれることがなく、鮮明な図柄などが得られ
る。Industrial Applicability The porous film of the present invention has the same level of moisture permeability as conventional products, is excellent in low strain elongation in the machine direction, is rich in flexibility, and has good hand. Therefore, it is useful as a material for sanitary articles worn on human skin such as disposable diapers and sanitary pads. In particular, when printing or the like is performed on the above-mentioned sanitary article, the pitch of printing is not shifted, and a clear pattern or the like is obtained because of excellent low strain elongation strength in the machine direction.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C08L 23/10 C08L 23/10 91/00 91/00 // B29K 23:00 B29K 23:00 105:04 105:04 B29L 7:00 B29L 7:00 (72)発明者 榎本 敏行 愛知県名古屋市南区丹後通2−1 三井化 学株式会社内 Fターム(参考) 4F071 AA16 AA18 AA20 AA71 AC12 AF07Y AF21Y AF26Y BA01 BB06 BB07 BB08 BB09 BC01 4F210 AA05 AA07 AA08 AA11 AB01 AB19 AG01 AG20 AR06 AR11 QC02 QG01 QG18 QW07 4J002 AE05Y BB03W BB03X BB05Z BB12W BB14W EP026 FD010──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C08L 23/10 C08L 23/10 91/00 91/00 // B29K 23:00 B29K 23:00 105: 04 105: 04 B29L 7:00 B29L 7:00 (72) Inventor Toshiyuki Enomoto 2-1 Tango-dori, Minami-ku, Nagoya-shi, Aichi F-term (reference) 4F071 AA16 AA18 AA20 AA71 AC12 AF07Y AF21Y AF26Y BA01 BB06 BB07 BB08 BB09 BC01 4F210 AA05 AA07 AA08 AA11 AB01 AB19 AG01 AG20 AR06 AR11 QC02 QG01 QG18 QW07 4J002 AE05Y BB03W BB03X BB05Z BB12W BB14W EP026 FD010
Claims (7)
及び無機充填材75〜45重量%を含む樹脂組成物から
成形された多孔性フィルムであって、ポリオレフィン系
樹脂が、密度0.930〜0.975の高密度ポリエチ
レン及びポリプロピレンから選ばれた少なくとも1種の
樹脂10〜70重量%、密度0.905〜0.930の
線形低密度ポリエチレン88〜15重量%、及び分岐状
低密度ポリエチレン2〜15重量%を含む多孔性フィル
ム。1. A polyolefin resin 25 to 55% by weight.
And a porous film formed from a resin composition containing 75 to 45% by weight of an inorganic filler, wherein the polyolefin-based resin is at least one selected from high-density polyethylene and polypropylene having a density of 0.930 to 0.975. A porous film comprising 10-70% by weight of a seed resin, 88-15% by weight of a linear low density polyethylene having a density of 0.905-0.930, and 2-15% by weight of a branched low density polyethylene.
に対し、硬化ひまし油及び脱水ひまし油から選ばれた少
なくとも1種の分散剤0.5〜5重量部を含有する請求
項1記載の多孔性フィルム。2. The porous material according to claim 1, further comprising 0.5 to 5 parts by weight of at least one dispersant selected from hardened castor oil and dehydrated castor oil, based on 100 parts by weight of the resin composition according to claim 1. Film.
に対し、液状のエチレン−α−オレフィンオリゴマー
0.5〜5重量部を含有する請求項1記載の多孔性フィ
ルム。3. The porous film according to claim 1, comprising 0.5 to 5 parts by weight of a liquid ethylene-α-olefin oligomer based on 100 parts by weight of the resin composition according to claim 1.
に対し、エチレンビスステアリン酸アミド及びメチレン
ビスステアリン酸アミドから選ばれた少なくとも1種の
滑剤0.5〜10重量部を含有する請求項1記載の多孔
性フィルム。4. A resin composition according to claim 1, which contains 0.5 to 10 parts by weight of at least one lubricant selected from ethylene bisstearic acid amide and methylene bisstearic acid amide based on 100 parts by weight of the resin composition according to claim 1. Item 4. The porous film according to Item 1,
2)の機械方向の5%伸び強度及び少なくとも27g/
25mm/(g/m2)の機械方向の10%伸び強度か
ら選ばれた少なくとも1種の特性を有し、且つ、機械方
向の剛軟性が2.7mm/(g/m2)以下、透湿度が
1500g/m2・24h以上、目付けが10〜35g
/m2である請求項1記載の多孔性フィルム。5. At least 18 g / 25 mm / (g / m
2 ) 5% elongation strength in the machine direction of at least 27 g /
It has at least one property selected from 10% elongation strength in the machine direction of 25 mm / (g / m 2 ), and has a rigidity in the machine direction of 2.7 mm / (g / m 2 ) or less. Humidity of 1500 g / m 2 · 24 h or more, basis weight of 10 to 35 g
/ M 2 .
求項1記載の多孔性フィルム。6. The porous film according to claim 1, wherein the heat shrinkage in the machine direction is 3% or less.
孔性フィルムの製造方法であって、請求項1〜4のいず
れか1項に記載の樹脂組成物をフィルム成形し、得られ
たフィルムを少なくとも機械方向に1.5〜3倍延伸し
て多孔性フィルムとなし、次いで、90〜120℃にお
いて、機械方向の収縮率を10〜25%に制御しながら
少なくとも0.004分間熱固定することを特徴とする
多孔性フィルムの製造方法。7. A method for producing a porous film according to any one of claims 1 to 6, wherein the resin composition according to any one of claims 1 to 4 is formed into a film. The resulting film is stretched at least 1.5 to 3 times in the machine direction to form a porous film, and then at 90 to 120 ° C. for at least 0.004 minutes while controlling the shrinkage in the machine direction to 10 to 25%. A method for producing a porous film, comprising heat setting.
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JP2001046928A JP2002249622A (en) | 2001-02-22 | 2001-02-22 | Porous film and preparation method for the same |
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JP2001294717A (en) * | 2000-02-09 | 2001-10-23 | Mitsui Chemicals Inc | Polyolefin resin composition and polyolefin film obtained therefrom |
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JP2005343938A (en) * | 2004-05-31 | 2005-12-15 | Mitsubishi Plastics Ind Ltd | Porous film, separator for non-aqueous electrolyte cell and non-aqueous electrolyte cell |
JP2005343928A (en) * | 2004-05-31 | 2005-12-15 | Mitsubishi Plastics Ind Ltd | Porous film, separator for non-aqueous electrolyte cell and non-aqueous electrolyte cell |
JP2005343936A (en) * | 2004-05-31 | 2005-12-15 | Mitsubishi Plastics Ind Ltd | Porous film, separator for non-aqueous electrolyte cell and non-aqueous electrolyte cell |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999022930A1 (en) * | 1997-11-04 | 1999-05-14 | Tredegar Corporation | Textured, dimensionally stable microporous film and method of making same |
JP2001294717A (en) * | 2000-02-09 | 2001-10-23 | Mitsui Chemicals Inc | Polyolefin resin composition and polyolefin film obtained therefrom |
-
2001
- 2001-02-22 JP JP2001046928A patent/JP2002249622A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999022930A1 (en) * | 1997-11-04 | 1999-05-14 | Tredegar Corporation | Textured, dimensionally stable microporous film and method of making same |
JP2001294717A (en) * | 2000-02-09 | 2001-10-23 | Mitsui Chemicals Inc | Polyolefin resin composition and polyolefin film obtained therefrom |
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