JPH08176234A - Polypropylene resin for non-oriented film - Google Patents

Polypropylene resin for non-oriented film

Info

Publication number
JPH08176234A
JPH08176234A JP32262794A JP32262794A JPH08176234A JP H08176234 A JPH08176234 A JP H08176234A JP 32262794 A JP32262794 A JP 32262794A JP 32262794 A JP32262794 A JP 32262794A JP H08176234 A JPH08176234 A JP H08176234A
Authority
JP
Japan
Prior art keywords
polypropylene resin
film
mfr
resin
oriented 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.)
Pending
Application number
JP32262794A
Other languages
Japanese (ja)
Inventor
Masahiko Futaki
真佐彦 二木
Toshio Hoshino
利夫 星野
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.)
Tonen Chemical Corp
Original Assignee
Tonen Sekiyu Kagaku KK
Tonen Chemical Corp
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 Tonen Sekiyu Kagaku KK, Tonen Chemical Corp filed Critical Tonen Sekiyu Kagaku KK
Priority to JP32262794A priority Critical patent/JPH08176234A/en
Publication of JPH08176234A publication Critical patent/JPH08176234A/en
Pending legal-status Critical Current

Links

Landscapes

  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

PURPOSE: To obtain a polypropylene resin for a non-oriented film improved in longitudinal tearing strength, impact strength, transparency and surface gloss by degrading a specified PP resin in the presence of an organic peroxide. CONSTITUTION: 0.005-0.1 pt.wt. organic peroxide is added to 100 pts.wt. PP resin having a melt flow rate(MFR) of 0.5-5g/10min and an Mw/Mn ratio of 5-7 (Mw is the weightaverage molecular weight and Mn is the number-average molecular weight) and the obtained mixture is melt-kneaded at 180-260 deg.C to obtain the degraded product being a PP resin for a non-oriented film, having an MFR of 7-20g/10min and an Mw/Mn ratio of 5 or below.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、無延伸フィルム成形用
のポリプロピレン樹脂に関する。
FIELD OF THE INVENTION The present invention relates to a polypropylene resin for molding unstretched films.

【0002】[0002]

【従来の技術】従来、無延伸ポリプロピレンフィルム
(以下、CPPと略すことがある。)用のポリプロピレ
ン樹脂は、実用面からメルトフローレイト(MFR)が
5〜12
2. Description of the Related Art Conventionally, polypropylene resins for unstretched polypropylene films (hereinafter sometimes abbreviated as CPP) have a melt flow rate (MFR) of 5 to 12 from the practical viewpoint.

【外3】 しかし、このようなポリプロピレン樹脂は、通常の12
0〜150m/分程度の製膜速度で用いた場合、得られ
るCPPは、縦裂き(MD)強度、耐衝撃強度等の機械
的物性及び透明性、表面光沢性等の光学的物性が十分で
なく、そのものの改善が望まれていた。又、生産性を向
上する目的から、製膜速度を180m/分以上に迄上昇
させると、フィルムの縦方向(MD)への配向が大きく
なり、MDと横方向(TD)の物性の異方性が大きくな
ってしまう結果、得られるCPPは、特にMD強度、耐
衝撃強度が低下し、実用に耐えなくなるという問題があ
った。
[Outside 3] However, such polypropylene resin is
When used at a film-forming speed of about 0 to 150 m / min, the obtained CPP has sufficient mechanical properties such as longitudinal tear (MD) strength and impact strength, and optical properties such as transparency and surface gloss. However, there was a desire for improvement. Also, for the purpose of improving productivity, when the film forming speed is increased to 180 m / min or more, the orientation of the film in the machine direction (MD) becomes large, and the physical properties of MD and transverse direction (TD) are anisotropic. As a result, the resulting CPP has a problem in that the MD strength and the impact strength are lowered, and the CPP cannot be put to practical use.

【0003】[0003]

【発明が解決しようとする課題】本発明は、従来の通常
の製膜速度における上記の問題点を解決するばかりでな
く、製膜速度が180m/分以上の高速製膜において
も、得られるCPPが、良好な物性を保持するポリプロ
ピレン樹脂を提供することを目的とする。
The present invention not only solves the above-mentioned problems in the conventional ordinary film forming speed, but also obtains a CPP obtained even in a high speed film forming speed of 180 m / min or more. However, it is an object of the present invention to provide a polypropylene resin having good physical properties.

【0004】[0004]

【課題を解決するための手段】本発明者らは、鋭意研究
を行った結果、特定のMFR及び分子量分布を持つポリ
プロピレン樹脂を、有機過酸化物により減成することに
よって得られる特定のMFR及び分子量分布を示すポリ
プロピレン樹脂が、本発明の目的を達成し得ることを見
出して、本発明に到達した。
Means for Solving the Problems As a result of earnest studies, the present inventors have found that a specific MFR and a specific MFR obtained by degrading a polypropylene resin having a specific MFR and a molecular weight distribution with an organic peroxide. The present invention has been accomplished by finding that a polypropylene resin exhibiting a molecular weight distribution can achieve the object of the present invention.

【0005】すなわち、本発明は、メルトフローレイト
(MFR)が0.5〜5g/10分
That is, the present invention has a melt flow rate (MFR) of 0.5 to 5 g / 10 minutes.

【外4】 旨とする。[Outside 4] To the effect.

【0006】本発明で用いられるポリプロピレン樹脂
は、プロピレンを主成分とする重合体であり、ホモポリ
プロピレン以外に、プロピレンと5重量%程度迄のエチ
レン,1ーブテン、1ーヘキセン等の他のオレィンとの
共重合体も含まれる。
The polypropylene resin used in the present invention is a polymer containing propylene as a main component, and other than homopolypropylene, propylene and other oleins such as ethylene, 1-butene and 1-hexene up to about 5% by weight. Copolymers are also included.

【0007】このポリプロピレン樹脂は、特定のメルト
フローレイト(MFR)と分子量分布を持つことが必要
であり、MFR(JIS K7210;荷重2.16k
g,230℃で測定)が0.5〜5g/10分、好まし
くは1〜4g/10分、分子
This polypropylene resin is required to have a specific melt flow rate (MFR) and molecular weight distribution, and MFR (JIS K7210; load 2.16k).
g, measured at 230 ° C.) is 0.5 to 5 g / 10 min, preferably 1 to 4 g / 10 min, molecule

【外5】 ことが工業的に困難となると共に、その規定値に調節し
たとしても本発明の目的が達成できず、いずれも好まし
くない。
[Outside 5] Is industrially difficult, and even if the specified value is adjusted, the object of the present invention cannot be achieved, and neither is preferable.

【0008】上記ポリプロピレン樹脂(以下、原料PP
という。)を減成するために用いられる有機過酸化物と
しては、ジt−ブチルパーオキサイド、t−ブチルクミ
ルパーオサイド、ジクミルパーオキサイド、α,α′−
ビス(t−ブチルパーオキシ−m−イソプロピル)ベン
ゼン、2,5−ジメチル−2,5−ジ(t−ブチルパー
オキシ)ヘキサン、2,5−ジメチル−2,5−ジ(t
−ブチルパーオキシ)−3−ヘキセン等が挙げられる。
The above polypropylene resin (hereinafter referred to as raw material PP
Say. Examples of the organic peroxide used for degrading) include di-t-butyl peroxide, t-butylcumylperoxide, dicumyl peroxide, α, α′-
Bis (t-butylperoxy-m-isopropyl) benzene, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane, 2,5-dimethyl-2,5-di (t
-Butylperoxy) -3-hexene and the like.

【0009】これら有機過酸化物を用いて原料PPを減
成する方法は、本発明の目的物である無延伸フィルム用
ポリプロピレン樹脂(以下、製品PPという。)が要求
する
The method of degrading the raw material PP using these organic peroxides is required by the polypropylene resin for an unstretched film (hereinafter referred to as the product PP) which is the object of the present invention.

【外6】 定されるものではないが、通常は原料PPに原料PP1
00重量部当り前記有機過酸化物を0.005〜0.1
0重量部加え、押出機中等において、通常、樹脂を溶融
させる温度、例えば180〜260℃で、溶融混練する
ことにより行われる。
[Outside 6] Although it is not specified, the raw material PP is usually added to the raw material PP1.
0.005 to 0.1 parts by weight of the organic peroxide is added per 100 parts by weight.
In addition to 0 parts by weight, it is usually carried out in an extruder or the like by melt-kneading at a temperature for melting the resin, for example, 180 to 260 ° C.

【0010】減成は、特に、製品PPのMFRを原料P
PのMFRの2〜30倍とするのが望ましい。又、必要
に応じて、減成の前に、原料PPに酸化防止剤、中和
剤、ブロッキング防止剤、滑り性付与剤等の添加剤を添
加しても良い。更に、有機過酸化物は、原料PP中での
分散性を良好にするために、適当な媒体で希釈したもの
を用いることもできる。
[0010] Degradation is made especially by using the MFR of the product PP as the raw material P.
It is desirable to be 2 to 30 times the MFR of P. Further, if necessary, additives such as an antioxidant, a neutralizing agent, an antiblocking agent and a slipperiness imparting agent may be added to the raw material PP before the degradation. Further, the organic peroxide may be diluted with an appropriate medium in order to improve the dispersibility in the raw material PP.

【0011】[0011]

【外7】 Pに製膜する時に押出性が劣り、良好な成形ができず、
20g/10分を超えると、ドローダウンが起り、製膜
性が問題となるばかりでなく、引裂強度、インパ
[Outside 7] When the film is formed on P, the extrudability is poor and good molding cannot be performed.
If it exceeds 20 g / 10 minutes, drawdown will occur and not only the film-forming property will become a problem, but also the tear strength and the impact strength

【外8】 械的物性及び光学的物性を持つCPPが得られず、いず
れも好ましくない。
[Outside 8] CPP having mechanical properties and optical properties cannot be obtained, and neither is preferable.

【0012】本発明のポリプロピレン樹脂(製品PP)
を用いて無延伸フィルムとする方法は、特定されるもの
ではなく、工業的に一般に行われている方法で行われ
る。
Polypropylene resin of the present invention (product PP)
The method of forming a non-stretched film by using is not specified, and a method generally used in industry is performed.

【0013】[0013]

【実施例】以下、本発明を実施例により、より詳細に説
明する。なお、例におけるパーセント(%)は、ヘイズ
とグロスの場合を除いて重量による。
EXAMPLES The present invention will now be described in more detail by way of examples. The percentages (%) in the examples are by weight except for the case of haze and gloss.

【0014】原料PP及び製品PP並びに無延伸フィル
ムの物性の測定は、下記の方法に従った。
The physical properties of the raw material PP, the product PP and the unstretched film were measured according to the following methods.

【0015】[0015]

【外9】 GPC(ゲルパーミエーションクロマトグラフィー)を
用いて測定。
[Outside 9] Measured using GPC (gel permeation chromatography).

【0016】ヘイズ ASTM D1003グロス JIS K7105引裂強度 ASTM D1922 MD強度は16枚のフィルムを重ねた値、TD強度は1
枚のフィルムの値。打抜衝撃強度 東洋精機社製フィルムインパクトテスターを使用。
Haze ASTM D1003 Gloss JIS K7105 Tear strength ASTM D1922 MD strength is a value obtained by stacking 16 films, and TD strength is 1.
The value for a sheet of film. Punching impact strength A film impact tester manufactured by Toyo Seiki Co., Ltd. is used.

【0017】23℃で、直径15mmの半球状衝撃頭を
用いて測定。
Measured at 23 ° C. using a hemispherical impact head with a diameter of 15 mm.

【0018】(実施例1〜3)表1に示す組成と物性を
持つ原料PP100重量部(以下、重量部)に、2,5
−ジメチル−2,5−ジ(t−ブチルパーオキシ)ヘキ
サン20%と流動パラフィン80%との混合物を表1に
示す量、更に酸化防止剤0.1部、中和剤0.05部、
ブロッキング防止剤0.1部及び滑り性付与剤0.1部
をそれぞれ添加し、ヘンシェルミキサーで十分に混合し
た。
(Examples 1 to 3) 100 parts by weight of a raw material PP having the composition and physical properties shown in Table 1 (hereinafter referred to as "parts by weight") was added with 2,5
-A mixture of 20% dimethyl-2,5-di (t-butylperoxy) hexane and 80% liquid paraffin shown in Table 1, 0.1 part of antioxidant, 0.05 part of neutralizing agent,
0.1 part of an antiblocking agent and 0.1 part of a slipperiness | lubricity imparting agent were added, respectively, and it fully mixed with a Henschel mixer.

【0019】このものを、50mmφ単軸押出機に供給
し、240℃で押出して、製品PPからなるペレットと
した。得られたペレットを用い、タンデム型押出機(1
50mmφ,90mmφ)を有する無延伸フィルム押出
機にて、240℃で押出した後、30℃の冷却ロールで
急冷して、製膜速度120m/分又は180m/分で巻
取り、厚さ25μmのフィルムに製膜した。
This product was supplied to a 50 mmφ single-screw extruder and extruded at 240 ° C. to obtain pellets made of product PP. Using the obtained pellets, a tandem extruder (1
A film having a thickness of 25 μm is obtained by extruding at 240 ° C. with an unstretched film extruder having 50 mmφ, 90 mmφ), rapidly cooling with a cooling roll at 30 ° C., and winding at a film forming speed of 120 m / min or 180 m / min. Was formed into a film.

【0020】得られたフィルムの物性を測定し、表2に
示した。
The physical properties of the obtained film were measured and are shown in Table 2.

【0021】(比較例1〜3)表1に示す組成と物性を
持つ原料PPを減成しないで用いるか、実施例3で用
(Comparative Examples 1 to 3) The raw material PP having the composition and physical properties shown in Table 1 is used without being degraded or used in Example 3.

【外10】 PPを用いる以外は、実施例1〜3と同様にして、無延
伸フィルムに製膜した。それらフィルムの物性を測定し
て表2に示した。
[Outside 10] A non-stretched film was formed in the same manner as in Examples 1 to 3 except that PP was used. The physical properties of these films were measured and are shown in Table 2.

【0022】[0022]

【表1】 [Table 1]

【表2】 [Table 2]

【0023】[0023]

【発明の効果】本発明のポリプロピレン樹脂を用いて得
た無延伸フィルムは、従来行われていた製膜速度(12
0〜150m/分)でのフィルム物性上の問題点である
縦裂き(MD)強度、耐衝撃強度、透明性及び表面光沢
性が大巾に改善されるばかりでなく、180m/分以上
という高速での製膜においても機械的強度が改善でき、
良好な物性を示し、かつ従来できなかった高速での良好
な製膜を可能とすることにより、大巾な生産性の向上が
図られる。
The unstretched film obtained by using the polypropylene resin of the present invention has a film-forming speed (12
(0-150 m / min) not only the longitudinal tear (MD) strength, impact strength, transparency and surface gloss, which are problems in film physical properties, are greatly improved, but also high speed of 180 m / min or more. The mechanical strength can be improved even in film formation at
By showing good physical properties and enabling high-speed good film formation, which was not possible in the past, a great improvement in productivity can be achieved.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 メルトフローレイト(MFR)が0.5
〜5g/10分、重 【外1】
1. A melt flow rate (MFR) of 0.5.
~ 5g / 10 minutes, heavy [External 1]
【請求項2】 【外2】 伸フィルム用ポリプロピレン樹脂。[Claim 2] Polypropylene resin for stretched film.
JP32262794A 1994-12-26 1994-12-26 Polypropylene resin for non-oriented film Pending JPH08176234A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32262794A JPH08176234A (en) 1994-12-26 1994-12-26 Polypropylene resin for non-oriented film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32262794A JPH08176234A (en) 1994-12-26 1994-12-26 Polypropylene resin for non-oriented film

Publications (1)

Publication Number Publication Date
JPH08176234A true JPH08176234A (en) 1996-07-09

Family

ID=18145832

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32262794A Pending JPH08176234A (en) 1994-12-26 1994-12-26 Polypropylene resin for non-oriented film

Country Status (1)

Country Link
JP (1) JPH08176234A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999062966A1 (en) * 1998-06-01 1999-12-09 Montell North America Inc. Propylene polymers suitable for transparent cast film
US6512050B2 (en) 2000-06-30 2003-01-28 Sumitomo Chemical Company, Limited Polypropylene resin composition, T die film made of the same and method of producing T die film

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999062966A1 (en) * 1998-06-01 1999-12-09 Montell North America Inc. Propylene polymers suitable for transparent cast film
US6440577B1 (en) 1998-06-01 2002-08-27 Basell Poliolefine Italia S.P.A. Propylene polymers suitable for transparent cast film
US6512050B2 (en) 2000-06-30 2003-01-28 Sumitomo Chemical Company, Limited Polypropylene resin composition, T die film made of the same and method of producing T die film
US6593003B2 (en) 2000-06-30 2003-07-15 Sumitomo Chemical Company, Limited Polypropylene resin composition, T die film made of the same and method of producing T die film

Similar Documents

Publication Publication Date Title
US6432496B1 (en) High density polyethylene films with improved barrier properties
US10300686B2 (en) Self-recyclable barrier packaging
US4500681A (en) Thermoplastic blend of polyolefin, isobutylene-backbone elastomer and ethylene copolymer
JPH09502473A (en) Batch inclusion package
JPH0222033A (en) Low temperature heat-shrinkable film
US7722961B2 (en) Resin composition and stretched film obtained by using the same
EP4029695A1 (en) Laminated film, and production method therefor
US4554321A (en) Film compositions of butene polymers
US5320899A (en) Thermoplastic block copolymer films
US7176259B1 (en) High density polyethylene films with improved barrier properties
US20050159532A1 (en) Processing aids for enhanced machine direction orientation rates and property enhancement of polyolefin films using hydrocarbon waxes
KR101664584B1 (en) Manufacturing method of polypropylene resin composition for higher shrinkage film
JPH08176234A (en) Polypropylene resin for non-oriented film
US4837074A (en) Thermoformed polyolefin articles having improved gloss
US5369181A (en) Olefinic polymer blends for improving polyolefins
EP0457568A2 (en) Polypropylene-polybutylene compositions
JP3215922B2 (en) Thermoplastic polyurethane resin composition
JPH10237239A (en) Resin composition for thermoforming and sheet made therefrom
KR20190061407A (en) Polyethylene resin composition and film comprising the same
JPH0853155A (en) Film which is easily tearable in longitudinal direction
JP4013497B2 (en) Polypropylene composition for film and film thereof
JPH08192462A (en) Opaque stretched film
JP4457594B2 (en) Polypropylene composition and film comprising the same
JPS59109543A (en) Ethylene copolymer resin composition for use in production of improved film
JPH11279342A (en) Resin composition