JPS6198756A - Hollow bottle with excellent low-temperature impact resistance - Google Patents
Hollow bottle with excellent low-temperature impact resistanceInfo
- Publication number
- JPS6198756A JPS6198756A JP59219395A JP21939584A JPS6198756A JP S6198756 A JPS6198756 A JP S6198756A JP 59219395 A JP59219395 A JP 59219395A JP 21939584 A JP21939584 A JP 21939584A JP S6198756 A JPS6198756 A JP S6198756A
- Authority
- JP
- Japan
- Prior art keywords
- polypropylene
- impact resistance
- low
- temperature impact
- weight
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
発明の分野
本発明は低温耐衝撃性に優れたポリプロピレン組成物に
関し、より詳細には中空瓶の用途に特に適したポリプロ
ピレン組成物忙関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention This invention relates to polypropylene compositions with excellent low temperature impact resistance, and more particularly to polypropylene compositions particularly suitable for hollow bottle applications.
従来技術及び解決すべき技術的課題
ポリプロピレンは剛性、透明性が良好であって且つ耐薬
品性及び衛生的特性に優れているため、中空瓶とし、て
の用途に着目されている。然しなから、中空瓶用徐には
ポリプロピレンの欠点である低温落下衝撃強度が要求さ
れるため、低温耐衝撃性の改良が必須不可欠である。PRIOR ART AND TECHNICAL PROBLEMS TO BE SOLVED Polypropylene has good rigidity and transparency, and is also excellent in chemical resistance and hygienic properties, so it is attracting attention for its use in hollow bottles. However, since polypropylene for hollow bottles is required to have low-temperature drop impact strength, which is a drawback of polypropylene, it is essential to improve the low-temperature impact resistance.
従来から、ポリプロピレンと他のポリオレフィンとのブ
レンドによる低温耐衝撃性改良の研究が進められている
が、剛性、透明性と低温耐衝撃性とは二律背反の関係に
あるため、このバランス調整に苦慮」、、ているのが現
状である。Research has been carried out to improve low-temperature impact resistance by blending polypropylene with other polyolefins, but since rigidity, transparency and low-temperature impact resistance have a trade-off relationship, it is difficult to balance them. The current situation is that...
発明の目的及び概要
即ち本発明の目的は、剛性、透明性とともに低温耐衝撃
性に優れたポリプロピレン組成物を提供するにある。OBJECT AND SUMMARY OF THE INVENTION An object of the present invention is to provide a polypropylene composition that has excellent rigidity, transparency, and low-temperature impact resistance.
本発明の他の目的は、中空瓶としての用途に特に適した
ポリプロピレン組成物を提供するにある。Another object of the invention is to provide a polypropylene composition particularly suitable for use as a hollow bottle.
本発明によれば、ポリプロピレン樹脂70乃至90重量
部、直鎖低密度ポリエチレン(以下LLDPEと呼ぶこ
とがある。)5乃至20重量部及び軟質エラストマー2
乃至20重量部とをブレンドして成る低温耐衝撃性に優
れたポリプロピレン組成物が提供される。According to the present invention, 70 to 90 parts by weight of polypropylene resin, 5 to 20 parts by weight of linear low density polyethylene (hereinafter sometimes referred to as LLDPE), and 2 parts by weight of soft elastomer.
A polypropylene composition having excellent low-temperature impact resistance is provided by blending 20 to 20 parts by weight of the polypropylene composition.
発明の構成
本発明において使用するポリプロピレン樹脂として(d
1ポリプロピレン単独重合体のみならず、ポリプロピレ
ンの有する透明性、剛性等の緒特性を損わない様な範囲
で他のオレフィンとのランダム共重合体を使用し得る。Structure of the Invention As the polypropylene resin used in the present invention (d
In addition to a polypropylene homopolymer, random copolymers with other olefins may be used as long as the properties of polypropylene such as transparency and rigidity are not impaired.
またこのポリプロピレン樹脂としては、密度が0.9[
1乃至0.915’/cdのものが好適に使用され、更
に成形性等の見地からメルトフローレート(以下MFR
とよぶ)が、0.1乃至3.0f/ 10min(AS
TM−D−1238の方法に準じ、190C5216C
1の荷重で測定した値、以下同じ)の範囲にあることが
好適である。In addition, this polypropylene resin has a density of 0.9[
1 to 0.915'/cd is preferably used, and from the viewpoint of moldability etc., the melt flow rate (hereinafter referred to as MFR) is preferably used.
) is 0.1 to 3.0f/10min (AS
According to the method of TM-D-1238, 190C5216C
The value measured under a load of 1 (hereinafter the same shall apply) is preferably within the range.
本発明において使用する直鎖低密度ポリエチレンは、通
常使用される高圧法低密度ポリエチレンや低圧法高密度
ポリエチレンには認められない幾つかの特徴を有してい
る。The linear low-density polyethylene used in the present invention has several characteristics that are not found in commonly used high-pressure low-density polyethylene and low-pressure high-density polyethylene.
即ち、高圧法低密度ポリエチレンは長鎖分岐を有する分
子構造で、エチレンの単一重合体であるのに対して、リ
ニア低密度ポリエチレンは実質上直鎖状の分子構造を有
し、しかるエチレンと炭素数4乃至8のα−オレフィン
との共重合体から成る。一方低圧法高密度ポリエチレン
は密度(25C)が0.940乃至0.965 f/c
rdの範囲にあり、その分子構造は短かい分岐鎖も殆ん
ど有(、ていないのに対して、リニア低密度ポリエチレ
ンは、密度が0.915乃至0.935r/cdの範囲
にあり、前述(−たα−オレフィンに由来する短頌分岐
鎖を有する点で相違している。That is, high-pressure low-density polyethylene has a molecular structure with long chain branches and is a single polymer of ethylene, whereas linear low-density polyethylene has a substantially straight-chain molecular structure and consists of ethylene and carbon. It consists of a copolymer with 4 to 8 α-olefins. On the other hand, low pressure high density polyethylene has a density (25C) of 0.940 to 0.965 f/c
rd range, and its molecular structure has almost no short branched chains, whereas linear low density polyethylene has a density in the range of 0.915 to 0.935 r/cd, It is different in that it has a short branched chain derived from the α-olefin mentioned above.
このリニア低密度ポリエチレンにおける共単量体として
は、ブテン−1、ペンテン−1,4−メチルペンテン−
1、ヘキセン−L 2−メチル−ブテン−1、オクテン
−1等の炭素数4乃至8のα−オレフィンを挙げること
ができ、これらのα−オレフィンは全体当り1乃至20
重量%、特に6乃至15重tチの量で重合体鎖中に組込
まれている。Comonomers in this linear low density polyethylene include butene-1, pentene-1,4-methylpentene-
1, hexene-L 2-Methyl-butene-1, octene-1 and other α-olefins having 4 to 8 carbon atoms can be mentioned, and these α-olefins have 1 to 20 carbon atoms per total.
It is incorporated into the polymer chain in an amount of 6% to 15% by weight, especially 6 to 15% by weight.
このリニア低密度ポリエチレン(L−LDpE)け、上
述[−念化学栂造にも関連1−で他のオレフィン#l詣
、例えば高圧法低密度ポリエチレンCHP4LDI)E
)、高密度ポリエチレン(II D P E )、結晶
性プロピレンエチレン共重合体CPPE)等に比して、
次の第7表に示すような物性上の相違を有する。This linear low-density polyethylene (L-LDpE) is also used in other olefins as mentioned above [-Related to Nenka Togazo, for example, high-pressure low-density polyethylene CHP4LDI]
), high density polyethylene (IIDPE), crystalline propylene ethylene copolymer CPPE), etc.
They have differences in physical properties as shown in Table 7 below.
第7表゛
樹 1町 伸び(係) 強度(Kq、y飼) 融点
<C)L−LDPE 850’ 、soo
10’/) 〜122UP−ILDPE (SO
D ’170 ” 94〜114HDPE
8[’]0 230”−118〜13ろP
PE 800 330 125〜153
上記第A表からポリプロピレン樹脂とブレンドするリニ
ア低密度ポリエチレンは、大きい伸び及び強度を有1−
ながら、低い融点を有するという特徴を有することが明
らかとなる。Table 7 Tree 1 Town Elongation (related) Strength (Kq, y) Melting point <C) L-LDPE 850', soo
10'/) ~122UP-ILDPE (SO
D '170'' 94~114HDPE
8[']0 230"-118~13roP
PE 800 330 125-153
From Table A above, linear low density polyethylene blended with polypropylene resin has high elongation and strength.
However, it is clear that it has the characteristic of having a low melting point.
本発明においては、これらのリニア低密度ポリ、r−f
−v ン(7)内f モM F Rカ0.1 乃’M
1’−0? / 10m−のものが好適に使用される。In the present invention, these linear low density poly, r-f
-v n (7) f mo M F R ka 0.1 乃'M
1'-0? /10 m- is preferably used.
更に本発明において使用する軟質エラストマーとしでは
エチレンとプロピ1/ン、ブテン、ヘキセン、オクテン
、デセン等のすtノフィンとの共重合体エラストマー、
プロピ1/ンμブテン、ヘキセ゛/、オクテン、デセン
等との共重合体エラストマー、ブテンとヘキセン、オク
テン、デセンg、cの共9合体エラストマー及びヘキセ
ンとオクテーン、デセン等との共重合体エラストマー等
が好適に使用され、特に密度が0.87乃至0.89
Y/crt1..11び、5fFRが0.1乃至40f
/10mmの範囲にあるものが好ましい。Furthermore, the soft elastomers used in the present invention include copolymer elastomers of ethylene and monofins such as propylene, butene, hexene, octene, and decene;
Copolymer elastomers of propylene/μ butene, hexene/, octene, decene, etc.; co-9 copolymer elastomers of butene and hexene, octene, decene g, c; copolymer elastomers of hexene, octene, decene, etc. are preferably used, especially those with a density of 0.87 to 0.89
Y/crt1. .. 11 and 5fFR is 0.1 to 40f
/10 mm is preferable.
本発明に訃いては、上記ポリプロピレン樹脂70乃至9
0重量部、特に75乃至85重合部、7、7. D P
E 5乃至25重量部、特に15乃至20f量部、及
び軟質エラストマー2乃至20重号部、特に5乃至10
重量部をブレンド1.てポリプロピレン組成物とする。According to the present invention, the above polypropylene resin 70 to 9
0 parts by weight, especially 75 to 85 polymerized parts, 7,7. D P
E 5 to 25 parts by weight, especially 15 to 20 parts by weight, and 2 to 20 parts by weight of soft elastomer, especially 5 to 10 parts by weight.
Blend parts by weight 1. to prepare a polypropylene composition.
本発明におけるかかるポリプロピレン組成物は、剛性、
透明性等に優れているととく、に、後述中る例に示す通
り、低温6て訃ける耐衝化性が顕著に向上し、特に中空
瓶としての用途に適用される。Such a polypropylene composition in the present invention has rigidity,
In addition to excellent transparency, as shown in the examples below, impact resistance at low temperatures is significantly improved, making it particularly suitable for use as hollow bottles.
ポリプロピレン樹脂の使用量が上記範囲よりも多くなる
と低温時の耐@冷性において不満足な本のとなり、また
少ない場合にはポリプロピレン特有の剛性、透明性等に
おいて不満足なものとなる。If the amount of polypropylene resin used is greater than the above range, the resulting product will be unsatisfactory in terms of cold resistance at low temperatures, and if it is less than the above range, the resulting product will be unsatisfactory in terms of rigidity, transparency, etc. specific to polypropylene.
従ってLLDPE及び軟質エラストマーが上記範囲より
イ、少ない場合、或いは多い場合にも同様の不都合を生
ずる。即ち、前述した配合比に応じてポリプロピレン(
耐脂、LLDPE及び軟質エラストマーをブレンドする
ことによって剛性、透明性及び低温耐衝撃性の組み合わ
せ特性に優れたポリプロピレン組成物が得られるのであ
る。Therefore, similar problems will occur if the amount of LLDPE and soft elastomer is less than or greater than the above range. That is, polypropylene (
By blending grease-resistant, LLDPE, and soft elastomers, polypropylene compositions with excellent combinations of stiffness, transparency, and low-temperature impact resistance are obtained.
本発明においてこれら成分のブレンド方式としては、固
体状成分を機械的に混合する方法、メルト状態でブレン
ドする方法、溶液状態でブ1/ンドする方法等の種々の
方法を採用し得るが、メルト状態でブレンドする方法が
最も好適である。In the present invention, various methods can be used to blend these components, such as mechanically mixing the solid components, blending them in a melt state, blending them in a solution state, etc. The method of blending in the state is most suitable.
本発明を次の例で説明する。The invention is illustrated by the following example.
実施例1゜
ポリプロピレン樹脂としてポリプロピレンのホモ重合体
(MF RO,5t/ 10顧、密度0.91f/ c
rl )を使用し、L−LDPE (i、fFR2,0
=i/1Qmin、密度0.9211 tlcrd)及
び軟質エラストマー(MF RO,4f/10酊、密度
0.880S’/cril )とを下記笥1表の配合に
従いメルトブレンドしてポリプロピレン組成物(試料1
〜5)を調製した。Example 1 Polypropylene homopolymer (MF RO, 5t/10cm, density 0.91f/c) was used as the polypropylene resin.
rl ) and L-LDPE (i, fFR2,0
= i/1Qmin, density 0.9211tlcrd) and a soft elastomer (MF RO, 4f/10mm, density 0.880S'/cril) according to the formulation shown in Table 1 below to prepare a polypropylene composition (sample 1).
-5) were prepared.
第 1 表
この組成物を用いてプロー成形及びシート成形によりそ
れぞれ円筒瓶(400CC1202、厚み0、7 m
)、シート(厚み2〜3−cm )を成形し、各種物性
を測定した。その結果を第2表に示す。Table 1 Using this composition, cylindrical bottles (400CC1202, thickness 0, 7 m) were prepared by blow molding and sheet molding, respectively.
), a sheet (2 to 3 cm thick) was molded, and various physical properties were measured. The results are shown in Table 2.
実施例2゜
ポリプロピレン樹脂としてポリプロピレンのランダム共
重合体(MF RO,5? / 10m1n、密度0.
91 tlcrd)を使用した以外は実施例1の試料1
〜6と同様の配合によりポリプロピl/ン組成物を調製
しく試料6.7.8 )、同様にして中空瓶及びシート
’t’?’:fだ。これらの各種物性を第2表に併せて
示す。Example 2 Polypropylene resin was a random copolymer of polypropylene (MF RO, 5?/10 m1n, density 0.
Sample 1 of Example 1 except that 91 tlcrd) was used.
A polypropylene composition was prepared by the same formulation as Sample 6.7.8), and a hollow bottle and a sheet 't' were prepared in the same manner. ':f. These various physical properties are also shown in Table 2.
実施例6゜
ポリプロピレン樹脂としてポリプロピレンのブロック共
重合体(、LfF R0,5? / 10m1n、密度
0、91 ? /crtl )を使用した以外は、実施
例1の試料1と同様にしてポリプロピレン組成物を調製
しく試料9)、同様にして中空瓶及びシートを得た。Example 6 A polypropylene composition was prepared in the same manner as Sample 1 of Example 1, except that a polypropylene block copolymer (LfF R0,5?/10 m1n, density 0,91?/crtl) was used as the polypropylene resin. Sample 9) was prepared, and a hollow bottle and sheet were obtained in the same manner.
この物性を第2表に示す。The physical properties are shown in Table 2.
実施例4゜
比較のために、ポリプロピレンのホモ重合体(A#R0
,5r、/10順、密度0.91ヲ10tl)、ランタ
ム共重合体CMFR0,5?/10mm 密度0、9
15’ /crtL )、及びブロック共重合体(AI
P RO,5?/ 10mt/I、密度0.915’
/C+4)をそれぞれ単独で使用して中空瓶及びシート
を得た(試料10.11.12)。これらの各社物性を
第2表に示す。Example 4 For comparison, a polypropylene homopolymer (A#R0
, 5r, /10 order, density 0.91 10 tl), Rantam copolymer CMFR0,5? /10mm Density 0, 9
15'/crtL), and block copolymer (AI
PRO, 5? / 10mt/I, density 0.915'
/C+4) were used alone to obtain hollow bottles and sheets (sample 10.11.12). Table 2 shows the physical properties of each of these companies.
Claims (2)
密度ポリエチレン5乃至20重量部及び軟質エラストマ
ー2乃至20重量部とをブレンドして成る低温耐衝撃性
に優れたポリプロピレン組成物。(1) A polypropylene composition with excellent low-temperature impact resistance, which is made by blending 70 to 90 parts by weight of a polypropylene resin, 5 to 20 parts by weight of linear low-density polyethylene, and 2 to 20 parts by weight of a soft elastomer.
重合体或いはポリプロピレンと他のオレフィンとのラン
ダム共重合体である特許請求の範囲第1項記載のポリプ
ロピレン組成物。(2) The polypropylene composition according to claim 1, wherein the polypropylene resin is a homopolymer of polypropylene or a random copolymer of polypropylene and another olefin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59219395A JPS6198756A (en) | 1984-10-20 | 1984-10-20 | Hollow bottle with excellent low-temperature impact resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59219395A JPS6198756A (en) | 1984-10-20 | 1984-10-20 | Hollow bottle with excellent low-temperature impact resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6198756A true JPS6198756A (en) | 1986-05-17 |
JPH0588264B2 JPH0588264B2 (en) | 1993-12-21 |
Family
ID=16734739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59219395A Granted JPS6198756A (en) | 1984-10-20 | 1984-10-20 | Hollow bottle with excellent low-temperature impact resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6198756A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993001236A1 (en) * | 1990-02-13 | 1993-01-21 | Monsanto Japan Limited | Thermoplastic elastomer composition |
WO1994006859A1 (en) * | 1992-09-15 | 1994-03-31 | The Dow Chemical Company | Impact modification of thermoplastics |
US5326639A (en) * | 1989-08-23 | 1994-07-05 | Himont Incorporated | Thermoplastic olefin polymer and method of preparing same |
US5468809A (en) * | 1992-02-24 | 1995-11-21 | Montell North America Inc. | Polyolefin compositions having good transparency and impact resistance |
JP2006316267A (en) * | 2005-05-10 | 2006-11-24 | Sk Corp | Polypropylene composition having excellent impact resistance, flexural modulus, and transparency, and product produced from the composition |
WO2014178249A1 (en) * | 2013-04-30 | 2014-11-06 | キョーラク株式会社 | Container |
WO2019044678A1 (en) * | 2017-08-31 | 2019-03-07 | キョーラク株式会社 | Delamination container |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57115440A (en) * | 1980-11-13 | 1982-07-17 | Bp Chimie Sa | High impact strength polypropylene composition |
JPS5880335A (en) * | 1981-11-10 | 1983-05-14 | Showa Denko Kk | resin composition |
JPS58101135A (en) * | 1981-12-10 | 1983-06-16 | Idemitsu Petrochem Co Ltd | Polypropylene composition |
JPS5943043A (en) * | 1982-09-02 | 1984-03-09 | Asahi Chem Ind Co Ltd | Resin composition for film molding |
-
1984
- 1984-10-20 JP JP59219395A patent/JPS6198756A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57115440A (en) * | 1980-11-13 | 1982-07-17 | Bp Chimie Sa | High impact strength polypropylene composition |
JPS5880335A (en) * | 1981-11-10 | 1983-05-14 | Showa Denko Kk | resin composition |
JPS58101135A (en) * | 1981-12-10 | 1983-06-16 | Idemitsu Petrochem Co Ltd | Polypropylene composition |
JPS5943043A (en) * | 1982-09-02 | 1984-03-09 | Asahi Chem Ind Co Ltd | Resin composition for film molding |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5326639A (en) * | 1989-08-23 | 1994-07-05 | Himont Incorporated | Thermoplastic olefin polymer and method of preparing same |
WO1993001236A1 (en) * | 1990-02-13 | 1993-01-21 | Monsanto Japan Limited | Thermoplastic elastomer composition |
US5468809A (en) * | 1992-02-24 | 1995-11-21 | Montell North America Inc. | Polyolefin compositions having good transparency and impact resistance |
WO1994006859A1 (en) * | 1992-09-15 | 1994-03-31 | The Dow Chemical Company | Impact modification of thermoplastics |
EP0877050A3 (en) * | 1992-09-15 | 1999-08-25 | The Dow Chemical Company | Impact modification of thermoplastics |
JP2006316267A (en) * | 2005-05-10 | 2006-11-24 | Sk Corp | Polypropylene composition having excellent impact resistance, flexural modulus, and transparency, and product produced from the composition |
WO2014178249A1 (en) * | 2013-04-30 | 2014-11-06 | キョーラク株式会社 | Container |
JP2014213934A (en) * | 2013-04-30 | 2014-11-17 | キョーラク株式会社 | Container |
WO2019044678A1 (en) * | 2017-08-31 | 2019-03-07 | キョーラク株式会社 | Delamination container |
JP2019043604A (en) * | 2017-08-31 | 2019-03-22 | キョーラク株式会社 | Laminated release container |
Also Published As
Publication number | Publication date |
---|---|
JPH0588264B2 (en) | 1993-12-21 |
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