JPH05186600A - Method for mixing polypropylene resin - Google Patents

Method for mixing polypropylene resin

Info

Publication number
JPH05186600A
JPH05186600A JP387392A JP387392A JPH05186600A JP H05186600 A JPH05186600 A JP H05186600A JP 387392 A JP387392 A JP 387392A JP 387392 A JP387392 A JP 387392A JP H05186600 A JPH05186600 A JP H05186600A
Authority
JP
Japan
Prior art keywords
intrinsic viscosity
mixing
polymer
resin
melt
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.)
Granted
Application number
JP387392A
Other languages
Japanese (ja)
Other versions
JP3184587B2 (en
Inventor
Tadashi Asanuma
浅沼  正
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP387392A priority Critical patent/JP3184587B2/en
Publication of JPH05186600A publication Critical patent/JPH05186600A/en
Application granted granted Critical
Publication of JP3184587B2 publication Critical patent/JP3184587B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/005Processes for mixing polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/10Homopolymers or copolymers of propene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To enable the mixing of two polypropylene resins having greatly different mol.wts. CONSTITUTION:Two polypropylene resins having greatly different mol.wts. and intrinsic viscosities of which the ratio is at least 2.5 are mixed as follows: first the two resins are melt mixed in such amts. that the amt. of the resin having a higher viscosity is the same as or higher than that of the resin having a lower viscosity and then the resulting mixture is melt mixed with a melt of the lower-viscosity resin in an amt. lower than that of the mixture.

Description

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

【0001】[0001]

【産業上の利用分野】本発明はポリプロピレン樹脂の混
合方法に関する。詳しくは分子量の異なるポリプロピレ
ン樹脂の混合方法に関する。
FIELD OF THE INVENTION The present invention relates to a method for mixing polypropylene resins. Specifically, it relates to a method for mixing polypropylene resins having different molecular weights.

【0002】[0002]

【従来の技術】分子量の大きく異なる樹脂を混合するこ
とは困難であり、特に分子量の大きい樹脂の割合が少な
い場合に充分に混練するのは困難であり、押出機で混練
する場合には途中に細かいメッシュを入れたり、焼結金
属を導入して大きなシェアーをかけることが試みられて
いるが充分ではなく、通常回分重合で同じ重合系で分子
量の異なるポリマーを作ることで実質的に分子量の異な
るポリマーを混合することが行われている。
2. Description of the Related Art It is difficult to mix resins having greatly different molecular weights, especially when the proportion of resins having a large molecular weight is small, and it is difficult to sufficiently knead them. Attempts have been made to insert a fine mesh or introduce a sintered metal to give a large share, but this is not sufficient, and in general batch polymerization produces different polymers with different molecular weights, resulting in substantially different molecular weights. Blending of the polymers is done.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、上記重
合による方法も回分的に重合する必要があり、得られた
分子量の異なるポリマーを混合するという目的には利用
できないし、押出機にメッシュとか焼結金属を導入する
方法は大きなエネルギーを必要とする割にその効果は小
さい。
However, the above-mentioned polymerization method also requires batchwise polymerization and cannot be used for the purpose of mixing the obtained polymers having different molecular weights. The method of introducing a metal requires a large amount of energy but its effect is small.

【0004】[0004]

【課題を解決するための手段】本発明者らは上記問題を
解決してブツなどの発生のない分子量の異なる樹脂の混
合方法について鋭意探索し特定の方法が優れていること
を見出し本発明を完成した。
Means for Solving the Problems The inventors of the present invention found that the method of mixing resins having different molecular weights without generation of lumps and solving the above problems is excellent, and that a specific method is excellent. completed.

【0005】即ち本発明は、極限粘度の比が2.5 以上の
2つのポリプロピレン樹脂を混合する方法において、極
限粘度が大きい樹脂の割合が極限粘度の小さい樹脂と同
じかそれ以上となる様に混合したものを溶融混練したも
のと、該溶融混練した物の量より少ない量の極限粘度の
小さい樹脂を溶融したものをさらに混練することを特徴
とする分子量の異なるポリプロピレン樹脂の混合方法で
ある。
That is, according to the present invention, in a method of mixing two polypropylene resins having an intrinsic viscosity ratio of 2.5 or more, the proportion of the resin having a high intrinsic viscosity is the same as or higher than that of the resin having a low intrinsic viscosity. A method for mixing polypropylene resins having different molecular weights, characterized in that a melt-kneaded product and a melted resin having a lower intrinsic viscosity in an amount smaller than the melt-kneaded product are further kneaded.

【0006】本発明においてポリプロピレン樹脂とは、
プロピレンの単独重合体、プロピレンと他の炭素数2〜
20のα−オレフィンとのランダム或いはブロック共重合
体のどのようなものも利用でき、プロピレン単位の立体
構造としてはアイソタクティック構造、シンジオタクテ
ィック構造、あるいはアタクティック構造のものについ
て適用可能である。
In the present invention, polypropylene resin means
Homopolymer of propylene, propylene and other C2-C2
Any of random or block copolymers with 20 α-olefins can be used, and the steric structure of the propylene unit is applicable to isotactic structure, syndiotactic structure, or atactic structure. ..

【0007】本発明において重要なのは、溶融混練に際
して、常に 135℃のテトラハイドロナフタレン溶液で測
定した極限粘度が大きいポリマーの割合を多くして混合
することにあり、そうすることで分子量の大きいポリマ
ーが粒子化することの無いようにすることにある。従っ
て混練機に導入する混合物は極限粘度の大きいポリマー
が小さいポリマーより多くなる様に2つのポリマーが混
合される。ここで極限粘度の高いポリマーと低いポリマ
ーの割合は50:50 〜90:10 、好ましくは60:40〜80:20
である。極限粘度の高いポリマーと低いポリマーの極限
粘度の比率としては2.5 以上であり、2.5 未満では通常
の混合で充分に混合が可能であり本発明の方法を適用す
るまでもない。上限については特に制限はないが通常20
程度である。
What is important in the present invention is to always mix a large proportion of a polymer having a large intrinsic viscosity measured with a tetrahydronaphthalene solution at 135 ° C. during the melt-kneading so that a polymer having a large molecular weight can be obtained. It is to prevent it from becoming particles. Therefore, in the mixture introduced into the kneading machine, the two polymers are mixed so that the polymer having a high intrinsic viscosity is larger than the polymer having a small intrinsic viscosity. Here, the ratio of the polymer having a high intrinsic viscosity and the polymer having a low intrinsic viscosity is 50:50 to 90:10, preferably 60:40 to 80:20.
Is. The ratio of the intrinsic viscosity of the polymer having a high intrinsic viscosity to that of a polymer having a low intrinsic viscosity is 2.5 or more, and when the ratio is less than 2.5, it is possible to perform sufficient mixing by ordinary mixing, and it is not necessary to apply the method of the present invention. There is no particular upper limit, but it is usually 20
It is a degree.

【0008】本発明においてはついで、上記溶融混練物
にさらに、極限粘度の小さいポリマーの溶融物が混合さ
れる。混合方法としては両者を押出機のサイドから導入
して混合するか、あるいはギヤポンプとスタティックミ
キサーを組合わせた装置に導入することで行うことがで
きる。
In the present invention, the melt-kneaded product is further mixed with a melt of a polymer having a small intrinsic viscosity. The mixing method can be carried out by introducing both from the side of the extruder and mixing, or by introducing them into a device in which a gear pump and a static mixer are combined.

【0009】このさらに混合する極限粘度の低いポリマ
ーの混合量としては、溶融混練されたポリマーの量より
少ない量であることが必要であり、多くなると極限粘度
の高いポリマーが粒子化し、均一に混合されない。こう
することで25%より多い比率で極限粘度の大きいポリマ
ーを混合することが出来るが、さらに極限粘度の低いポ
リマーを混合することもでき、そうすることでさらに少
ない比率で極限粘度の大きいポリマーを混合することが
可能となる。
The amount of the polymer having a lower intrinsic viscosity to be further mixed needs to be smaller than the amount of the polymer melt-kneaded. When the amount is increased, the polymer having a high intrinsic viscosity is formed into particles and mixed uniformly. Not done. By doing so, it is possible to mix a polymer having a large intrinsic viscosity in a ratio of more than 25%, but it is also possible to mix a polymer having a lower intrinsic viscosity, and by doing so, a polymer having a larger intrinsic viscosity can be prepared in a smaller ratio. It becomes possible to mix.

【0010】混練機における温度としては比較的低温で
シェアーが掛かる状態で混合することが好ましい。通常
160〜 300℃、好ましくは 180〜 280℃である。
It is preferable that the temperature in the kneading machine is relatively low and the mixing is performed in a state where shearing is applied. Normal
The temperature is 160 to 300 ° C, preferably 180 to 280 ° C.

【0011】混練機として押出機を用いる場合には押出
機のL/D は比較的大きいものを利用するのが好ましく、
通常50〜500 、好ましくは80〜300 程度である。
When an extruder is used as the kneading machine, it is preferable to use one having a relatively large L / D.
It is usually 50 to 500, preferably about 80 to 300.

【0012】追加する極限粘度の小さいポリマーの導入
方法としては特に制限はないが通常本体より小型の押出
機あるいは、単に加熱ゾーンとギヤポンプからなる構造
のものを利用するのが一般的である。
There is no particular limitation on the method of introducing the additional polymer having a low intrinsic viscosity, but an extruder smaller than the main body or a structure having only a heating zone and a gear pump is generally used.

【0013】[0013]

【実施例】以下に実施例を示しさらに本発明を説明す
る。
EXAMPLES The present invention will be further described with reference to the following examples.

【0014】実施例1 市販の三井東圧化学(株)製のポリプロピレン(商品名
三井ノーブレン)を2種準備した。1 つは極限粘度が2.8
5のEPグレードであり、もう1つは1.10のJ4Hグレードで
ある。この2グレードを押出機サイドに40mmφの押出機
を設けた65mmφの押出機を用い、EPグレードとJ4H グレ
ードを50:50 で混合したものを40kg/hで押出しながらサ
イドからJ4H グレードを40kg/hで導入して混合し造粒し
た。ここで混練部の温度は 220℃であった。得られたペ
レットで厚さ30μm のフイルムを成形したところフイル
ムは均一であった。
Example 1 Two kinds of commercially available polypropylene (trade name: Mitsui Noblene, manufactured by Mitsui Toatsu Chemicals, Inc.) were prepared. One has an intrinsic viscosity of 2.8
5 is EP grade and the other is 1.10 J4H grade. Using the 65 mmφ extruder equipped with a 40 mmφ extruder on the side of these 2 grades, the mixture of EP grade and J4H grade at 50:50 is extruded at 40 kg / h, while J4H grade is 40 kg / h from the side. Was introduced, mixed and granulated. Here, the temperature of the kneading part was 220 ° C. A film having a thickness of 30 μm was formed from the obtained pellets, and the film was uniform.

【0015】比較例1 実施例1 で用いたEPグレードとJ4H グレードを 20:60の
比率で混合して押出機で 220℃で一度混練して得たペレ
ットについて同様にフイルムを作って評価したところブ
ツが多く観測され均一のフイルムとはならなかった。
Comparative Example 1 EP grades used in Example 1 and J4H grades were mixed at a ratio of 20:60 and once kneaded at 220 ° C. in an extruder. Many spots were observed and the film was not uniform.

【0016】[0016]

【発明の効果】本発明の方法を実施することにより分子
量が大きく異なるポリプロピレンを混合することがで
き、工業的に極めて価値がある。
By carrying out the method of the present invention, polypropylenes having greatly different molecular weights can be mixed, which is extremely valuable industrially.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 極限粘度の比が2.5 以上の2つのポリプ
ロピレン樹脂を混合する方法において、極限粘度が大き
い樹脂の割合が極限粘度の小さい樹脂と同じかそれ以上
となる様に混合したものを溶融混練したものと、該溶融
混練した物の量より少ない量の極限粘度の小さい樹脂を
溶融したものをさらに混練することを特徴とする分子量
の異なるポリプロピレン樹脂の混合方法。
1. A method of mixing two polypropylene resins having an intrinsic viscosity ratio of 2.5 or more, in which a mixture of resins having a high intrinsic viscosity is the same as or higher than a resin having a low intrinsic viscosity and melted. A method for mixing polypropylene resins having different molecular weights, characterized by further kneading a kneaded product and a melted product of a resin having an intrinsic viscosity smaller than that of the melt-kneaded product.
JP387392A 1992-01-13 1992-01-13 Mixing method of polypropylene resin Expired - Fee Related JP3184587B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP387392A JP3184587B2 (en) 1992-01-13 1992-01-13 Mixing method of polypropylene resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP387392A JP3184587B2 (en) 1992-01-13 1992-01-13 Mixing method of polypropylene resin

Publications (2)

Publication Number Publication Date
JPH05186600A true JPH05186600A (en) 1993-07-27
JP3184587B2 JP3184587B2 (en) 2001-07-09

Family

ID=11569309

Family Applications (1)

Application Number Title Priority Date Filing Date
JP387392A Expired - Fee Related JP3184587B2 (en) 1992-01-13 1992-01-13 Mixing method of polypropylene resin

Country Status (1)

Country Link
JP (1) JP3184587B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000058398A1 (en) * 1999-03-26 2000-10-05 Idemitsu Petrochemical Co., Ltd. Propylene resin composition and process for producing the same
JP2005325339A (en) * 2004-04-13 2005-11-24 Sumitomo Chemical Co Ltd Polypropylene resin composition and its production method
JP2011157564A (en) * 2004-04-13 2011-08-18 Sumitomo Chemical Co Ltd Polypropylene resin composition and manufacturing method for the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000058398A1 (en) * 1999-03-26 2000-10-05 Idemitsu Petrochemical Co., Ltd. Propylene resin composition and process for producing the same
JP2005325339A (en) * 2004-04-13 2005-11-24 Sumitomo Chemical Co Ltd Polypropylene resin composition and its production method
JP2011157564A (en) * 2004-04-13 2011-08-18 Sumitomo Chemical Co Ltd Polypropylene resin composition and manufacturing method for the same
US8278392B2 (en) 2004-04-13 2012-10-02 Sumitomo Chemical Company, Limited Process for producing propylene resin composition
US8293843B2 (en) 2004-04-13 2012-10-23 Sumitomo Chemical Company, Limited Process for producing propylene resin composition

Also Published As

Publication number Publication date
JP3184587B2 (en) 2001-07-09

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