JP2002179858A5 - - Google Patents

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JP2002179858A5
JP2002179858A5 JP2000377503A JP2000377503A JP2002179858A5 JP 2002179858 A5 JP2002179858 A5 JP 2002179858A5 JP 2000377503 A JP2000377503 A JP 2000377503A JP 2000377503 A JP2000377503 A JP 2000377503A JP 2002179858 A5 JP2002179858 A5 JP 2002179858A5
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JP
Japan
Prior art keywords
methyl
octadiene
polymerization
hexadiene
ethylene
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JP2000377503A
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Japanese (ja)
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JP2002179858A (en
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Description

【請求項5】
請求項1ないし4のいずれかに記載の改質ポリプロピレン組成物(A) 20〜99重量部と、
メルトフローレート(ASTM D1238、230℃、荷重2.16kg)が0.4
〜10g/10分の範囲にある非改質ポリプピレン(F) 80〜1重量部(但し、改質ポリプロピレン組成物(A)と非改質ポリプピレン(F)の合計は100重量部である。)とからなることを特徴とする改質ポリプロピレン組成物。
Claim 5.
20 to 99 parts by weight of the modified polypropylene composition (A) according to any one of claims 1 to 4,
Melt flow rate (ASTM D1238, 230 ° C, load 2.16 kg) is 0.4
Unmodified polyps and Russia pyrene in the range of to 10 g / 10 min (F) 1:80 parts by weight (however, the modified polypropylene composition (A) and the sum of the unmodified polyps and Russia pyrene (F) is 100 parts by weight The modified polypropylene composition characterized by the following.

【請求項7】
請求項1ないしのいずれかに記載の改質ポリプロピレン組成物(A)を発泡させて得られることを特徴とする改質ポリプロピレン発泡体。
7.
A modified polypropylene foam obtained by foaming the modified polypropylene composition (A) according to any one of claims 1 to 5 .

本発明の他の態様に係る改質ポリプロピレン組成物は、
前記改質ポリプロピレン組成物(A) 20〜99重量部と、
メルトフローレート(ASTM D1238、230℃、荷重2.16kg)が0.4
〜10g/10分の範囲にある非改質ポリプピレン(F) 80〜1重量部とからなることを特徴としている。
Modified polypropylene composition according to another aspect of the present invention,
20 to 99 parts by weight of the modified polypropylene composition (A),
Melt flow rate (ASTM D1238, 230 ° C, load 2.16 kg) is 0.4
It is characterized by comprising the unmodified polyps and Russia pyrene (F) 1:80 parts by weight in the range of to 10 g / 10 min.

本発明では、高分子量ポリエチレンは少量の上記エチレンおよび炭素原子数3〜20のα-オレフィン以外の不飽和単量体を含んでいてもよい。このような不飽和単量体として
は、1,3-ブタジエン、1,3-ペンタジエン、1,4-ペンタジエン、1,3-ヘキサジエン、1,4-ヘキサジエン、1,5-ヘキサジエン、4-メチル-1,4-ヘキサジエン、5-メチル-1,4-ヘキサジエン、6-メチル-1,6-オクタジエン、7-メチル-1,6-オクタジエン、6-エチル-1,6-オクタジ
エン、6-プロピル-1,6-オクタジエン、6-ブチル-1,6-オクタジエン、6-メチル-1,6-ノナ
ジエン、7-メチル-1,6-ノナジエン、6-エチル-1,6-ノナジエン、7-エチル-1,6-ノナジエ
ン、6-メチル-1,6-デカジエン、7-メチル-1,6-デカジエン、6-メチル-1,6-ウンデカジエ
ン、1,7-オクタジエン、1,9-デカジエン、イソプレン、ブタジエン、エチリデンノルボルネン、ビニルノルボルネンおよびジシクロペンタジエンなどの炭素原子数4〜20のジエン化合物などが挙げられる。これらの不飽和単量体から導かれる構成単位は、高分子量ポリエチレン中に2モル%以下、好ましくは1モル%以下の割合で含んでいてもよい。
In the present invention, the high molecular weight polyethylene may contain a small amount of the above-mentioned ethylene and an unsaturated monomer other than the α-olefin having 3 to 20 carbon atoms. Such unsaturated monomers include 1,3-butadiene, 1,3-pentadiene, 1,4-pentadiene, 1,3-hexadiene, 1,4-hexadiene, 1,5-hexadiene, 4-methyl -1,4-hexadiene, 5-methyl-1,4-hexadiene, 6-methyl-1,6-octadiene, 7-methyl-1,6-octadiene, 6-ethyl-1,6-octadiene, 6-propyl -1,6-octadiene, 6-butyl-1,6-octadiene, 6-methyl-1,6-nonadiene, 7-methyl-1,6-nonadiene, 6-ethyl-1,6-nonadiene, 7-ethyl -1,6-nonadiene, 6-methyl-1,6-decadiene, 7-methyl-1,6-decadiene, 6-methyl-1,6-undecadiene, 1,7-octadiene, 1,9-decadiene, isoprene And diene compounds having 4 to 20 carbon atoms such as butadiene, ethylidene norbornene, vinylnorbornene and dicyclopentadiene. The constituent units derived from these unsaturated monomers may be contained in the high-molecular-weight polyethylene at a ratio of 2 mol% or less, preferably 1 mol% or less.

(高分子量ポリエチレン(B))
本発明で用いられる高分子量ポリエチレン(B)は、エチレン単独重合体またはエチレンと炭素原子数が3〜20のα-オレフィンとの共重合体である。ここで、炭素原子数が
3〜20のα-オレフィンとしては、プロピレン、1-ブテン、1-ペンテン、1-ヘキセン、4-メチル-1-ペンテン、1-オクテン、1-デセン、1-ドデセン、1-テトラデセン、1-ヘキサデセン、1-オクタデセン、1-エイコセンなどが挙げられ、炭素原子数が3〜8のα-オレフ
ィンが好ましい。これらのα-オレフィンは、エチレンとランダム共重合体を形成しても
よく、また、ブロック共重合体を形成してもよい。これらのα-オレフィンから導かれる
構成単位は、高分子量ポリエチレン中に10モル%以下、好ましくは5モル%以下の割合で含んでいてもよい。
(High molecular weight polyethylene (B))
The high molecular weight polyethylene (B) used in the present invention is an ethylene homopolymer or a copolymer of ethylene and an α-olefin having 3 to 20 carbon atoms. Here, as the α-olefin having 3 to 20 carbon atoms, propylene, 1-butene, 1-pentene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene, 1-dodecene , 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene and the like, and an α-olefin having 3 to 8 carbon atoms is preferable. These α-olefins may form a random copolymer with ethylene, or may form a block copolymer. The constituent units derived from these α-olefins may be contained in the high molecular weight polyethylene in a proportion of 10 mol% or less, preferably 5 mol% or less.

本発明では、高分子量ポリエチレンは少量の上記エチレンおよび炭素原子数3〜20のα-オレフィン以外の不飽和単量体を含んでいてもよい。このような不飽和単量体として
は、1,3-ブタジエン、1,3-ペンタジエン、1,4-ペンタジエン、1,3-ヘキサジエン、1,4-ヘキサジエン、1,5-ヘキサジエン、4-メチル-1,4-ヘキサジエン、5-メチル-1,4-ヘキサジエン、6-メチル-1,6-オクタジエン、7-メチル-1,6-オクタジエン、6-エチル-1,6-オクタジ
エン、6-プロピル-1,6-オクタジエン、6-ブチル-1,6-オクタジエン、6-メチル-1,6-ノナ
ジエン、7-メチル-1,6-ノナジエン、6-エチル-1,6-ノナジエン、7-エチル-1,6-ノナジエ
ン、6-メチル-1,6-デカジエン、7-メチル-1,6-デカジエン、6-メチル-1,6-ウンデカジエ
ン、1,7-オクタジエン、1,9-デカジエン、イソプレン、ブタジエン、エチリデンノルボルネン、ビニルノルボルネンおよびジシクロペンタジエンなどの炭素原子数4〜20のジエン化合物などが挙げられる。これらの不飽和単量体から導かれる構成単位は、高分子量ポリエチレン中に2モル%以下、好ましくは1モル%以下の割合で含んでいてもよい。
In the present invention, the high molecular weight polyethylene may contain a small amount of the above-mentioned ethylene and an unsaturated monomer other than the α-olefin having 3 to 20 carbon atoms. Examples of such unsaturated monomers include 1,3-butadiene, 1,3-pentadiene, 1,4-pentadiene, 1,3-hexadiene, 1,4-hexadiene, 1,5-hexadiene, and 4-methyl -1,4-hexadiene, 5-methyl-1,4-hexadiene, 6-methyl-1,6-octadiene, 7-methyl-1,6-octadiene, 6-ethyl-1,6-octadiene, 6-propyl -1,6-octadiene, 6-butyl-1,6-octadiene, 6-methyl-1,6-nonadiene, 7-methyl-1,6-nonadiene, 6-ethyl-1,6-nonadiene, 7-ethyl -1,6-nonadiene, 6-methyl-1,6-decadiene, 7-methyl-1,6-decadiene, 6-methyl-1,6-undecadiene, 1,7-octadiene, 1,9-decadiene, isoprene And diene compounds having 4 to 20 carbon atoms such as butadiene, ethylidene norbornene, vinylnorbornene and dicyclopentadiene. The constituent units derived from these unsaturated monomers may be contained in the high-molecular-weight polyethylene at a ratio of 2 mol% or less, preferably 1 mol% or less.

本発明の改質ポリプロピレン組成物(A)は伸長変形時の粘度の急激な上昇があり、メルトテンションが高く、かつMFRが適度であることから、特に発泡シート状に成形することに適している。
本発明の改質ポリプロピレン組成物(A)から製造された発泡シートはドローダウンが少なく二次成形が良好であり、熱圧空成形または真空成形により、発泡シートからトレーなどを多量に成形することができる。
The modified polypropylene composition (A) of the present invention has a sharp rise in viscosity during elongation deformation, has a high melt tension, and has an appropriate MFR, and is therefore particularly suitable for molding into a foamed sheet. .
Foam sheets made from modified polypropylene composition (A) of the present invention has good secondary formability little drawdown, thermal pressure forming or vacuum forming, can be molded from foam sheet such as a large amount tray Can be.

【0076】
【発明の効果】
本発明に係る改質ポリロピレン組成物はメルトテンションが高く発泡性に適した溶融特性が優れている。本発明の改質ポリロピレン組成物は流動性が優れ、かつメルトテンションが高く、独立気泡からなる発泡シートが得られる。この発泡シートはドローダウンが少なく二次加工性が優れ、外観美麗な、耐熱性、食品衛生性に優れたカップ、トレーなどの発泡体を成形することができる。
[0076]
【The invention's effect】
Modified poly-flop propylene composition according to the present invention has excellent melt characteristics melt tension suitable for high foaming. Modified poly-flop propylene composition of the present invention is excellent in fluidity and melt tension is high, the foam sheet is obtained consisting of closed cells. This foam sheet can form a foam such as cups and trays having a small drawdown, excellent secondary workability, excellent appearance, excellent heat resistance, and excellent food hygiene.

引き続き、重合機内の窒素を真空ポンプで除去し、プロピレンを装入しつつ、昇温を開始し、重合温度を70℃とし内圧6kg/cm2(ゲージ)上限とし無水素濃度下でプロ
ピレを連続的に装入し、所定量のプロピレンを反応させた。重合終了後メタノールを144.3ml装入して重合を停止させ、通常の方法により精製乾燥して、520kgのパウダー重合体を得た。得られたポリプロピレンの[η]は7.2dl/gであり、赤外吸収測定から求めたエチレン量は7.0重量%であった。
Subsequently, the polymerization flight nitrogen was removed by a vacuum pump, while charged with propylene, the Atsushi Nobori was started, the polymerization temperature was 70 ° C. internal pressure 6 kg / cm 2 (gauge) upper and pro under no hydrogen concentration <br /> the Pile down continuously charged, allowed to react a predetermined amount of propylene. After the completion of the polymerization, 144.3 ml of methanol was charged to stop the polymerization, and the resultant was purified and dried by a usual method to obtain 520 kg of a powder polymer. [Η] of the obtained polypropylene was 7.2 dl / g, and the amount of ethylene determined by infrared absorption measurement was 7.0% by weight.

【0085】
【比較例1】
ポリプロピレン組成物
内容量3000リットルの重合装置に窒素雰囲気下で、ヘプタン1180リットル、トリエチルアルミニウム11gと実施例1の方法で調整した固体状チタン媒成分を78g
装入した。重合槽内の窒素0kg/cm2(ゲージ)下で、エチレンを装入を開始した。
上限温度35℃で重合槽の内圧を3kg/cm2(ゲージ)上限で反応予定量のエチレン
を連続的に装入し、残圧反応も含め3時間重合を継続した。重合槽残圧0kg/cm2
ゲージ)付近で重合槽内のスラリーの一部をサンプリングして分析したところ、[η]は35.0dl/gであった。
[0085]
[Comparative Example 1]
Under a nitrogen atmosphere in the polypropylene composition content weight of 3,000 liters polymerization apparatus, heptane 1,180 liters, triethylaluminum 11g of the solid titanium catalysts components adjusted by the method of Example 1 78 g
Charged. Under a nitrogen atmosphere of 0 kg / cm 2 (gauge) in the polymerization tank, ethylene charging was started.
At an upper limit temperature of 35 ° C. and an internal pressure of the polymerization tank of 3 kg / cm 2 (gauge), an expected amount of ethylene was continuously charged at an upper limit, and polymerization was continued for 3 hours including a residual pressure reaction. Polymerization tank residual pressure 0 kg / cm 2 (
A part of the slurry in the polymerization tank was sampled and analyzed near (gauge), and [η] was 35.0 dl / g.

引き続き、トリエチルアルミニウム148g、DCPMS 299gとを重合機に追加
し、重合機内の窒素を真空ポンプで除去し、プロピレンを装入しつつ昇温を開始し、重合温度を70℃で内圧6kg/cm2(ゲージ)上限とし無水素濃度下でプロピレを連続
的に装入し、所定量のプロピレンを反応させた。重合終了後メタノールを144.3ml装入して重合を停止させ、通常の方法により精製乾燥して、500kgのパウダー重合体を得た。得られたポリプロピレンの[η]は6.7dl/gであり、赤外吸収測定から求めエチレン含量は0.9重量%であった。
Subsequently, triethyl aluminum 148 g, was added and DCPMS 299 g to polymerizer, polymerization flight nitrogen was removed by a vacuum pump, to begin heated while charged with propylene, pressure 6 kg / cm 2 and the polymerization temperature at 70 ° C. (gauge) the upper limit and then propylene down under no hydrogen concentration continuously charged, allowed to react a predetermined amount of propylene. After completion of the polymerization, 144.3 ml of methanol was charged to stop the polymerization, and the polymer was purified and dried by a usual method to obtain 500 kg of a powder polymer. [Η] of the obtained polypropylene was 6.7 dl / g, and the ethylene content determined by infrared absorption measurement was 0.9% by weight.

得られた発泡シートの発泡倍率、外観、セル形状および二次成形性(真空成形性)につき評価した。結果を表2に示す。
シート外観:目視で評価基準により評価した。
外観の評価基準:
○:未発泡部位や凹凸、コルゲート見られない。

The expansion ratio, appearance, cell shape and secondary formability (vacuum formability) of the obtained foamed sheet were evaluated. Table 2 shows the results.
Sheet appearance: visually evaluated according to evaluation criteria.
Evaluation criteria for appearance:
:: Unfoamed portions, irregularities, and corrugates are not observed.

JP2000377503A 2000-12-12 2000-12-12 Modified polypropylene composition, method for producing the same, modified polypropylene foam and method for producing the same Withdrawn JP2002179858A (en)

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JP2000377503A JP2002179858A (en) 2000-12-12 2000-12-12 Modified polypropylene composition, method for producing the same, modified polypropylene foam and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000377503A JP2002179858A (en) 2000-12-12 2000-12-12 Modified polypropylene composition, method for producing the same, modified polypropylene foam and method for producing the same

Publications (2)

Publication Number Publication Date
JP2002179858A JP2002179858A (en) 2002-06-26
JP2002179858A5 true JP2002179858A5 (en) 2006-11-09

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Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9187610B2 (en) 2004-10-27 2015-11-17 Sumitomo Chemical Company, Limited Polypropylene resin composition and foamed article produced therefrom
JP5893181B2 (en) * 2015-01-26 2016-03-23 株式会社プライムポリマー Propylene resin composition for welding molding and welded molding obtained therefrom

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