JPS6128538A - Low-density polyethylene resin composition - Google Patents

Low-density polyethylene resin composition

Info

Publication number
JPS6128538A
JPS6128538A JP14931484A JP14931484A JPS6128538A JP S6128538 A JPS6128538 A JP S6128538A JP 14931484 A JP14931484 A JP 14931484A JP 14931484 A JP14931484 A JP 14931484A JP S6128538 A JPS6128538 A JP S6128538A
Authority
JP
Japan
Prior art keywords
density polyethylene
weight
ethylene
molecular weight
resin composition
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
JP14931484A
Other languages
Japanese (ja)
Other versions
JPH0430420B2 (en
Inventor
Akira Tokura
戸倉 昭
Misao Mukui
椋井 美佐夫
Toshihiro Furusawa
古沢 俊宏
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.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical Co Ltd
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 Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP14931484A priority Critical patent/JPS6128538A/en
Publication of JPS6128538A publication Critical patent/JPS6128538A/en
Publication of JPH0430420B2 publication Critical patent/JPH0430420B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:The titled resin composition which has excellent high-speed processing characteristics and excellent heat-sealing strength, etc. and is suitable for use as a food packaging material, etc., obtained by mixing an ethylene/alpha-olefin copolymer and a high-pressure low-density polyethylene. CONSTITUTION:90-50wt% ethylene/alpha-olefin copolymer (e.g. an ethylene-propylene copolymer or an ethylene/1-butene copolymer) having a density of 0.9- 0.94g/ cm<3> and a melt index of 1-25g/10min, and 10-50wt% high-pressure low- density polyethylene having a ratio of the weight-average molecular weight to the number-average molecular weight of 4-15, a weight-average molecular weight of 50,000-300,000, and a fraction of a molecular weight of 50,000 or higher of 5-24wt% are kneaded sufficiently using a Banbury mixer, an extruder, etc. by multi-melt-compounding, simple melt-compounding, etc. to give an objective low-density polyethylene resin composition.

Description

【発明の詳細な説明】 本発明は低密度ポリエチレン樹脂組成物に関し、詳しく
は高速加工性にすぐれ、かつヒートシール強度等にすぐ
れた低密度ポリエチレン樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low-density polyethylene resin composition, and more particularly to a low-density polyethylene resin composition that has excellent high-speed processability and excellent heat-sealing strength.

一般k、直鎖低密度ポリエチレンフィルムはヒートシー
ル強度、夾雑物シール強度、ホットタック性4どが良好
であるが、反面その狭い分子量分布、と分子構造の直鎖
性に起因して高速加工性に劣るという欠点がある。特に
、この高速加工性が不良であるという欠点は該フィルム
な押出ラミネート加工に供する際に顕著に現われ、樹脂
膜の幅や厚さが変動する、いわゆるドローレゾナンス現
象を呈するため、商品価値を著しく損う。
In general, linear low-density polyethylene film has good heat sealing strength, impurity sealing strength, and hot tack property4, but on the other hand, it is difficult to process at high speed due to its narrow molecular weight distribution and linearity of the molecular structure. It has the disadvantage of being inferior to In particular, this drawback of poor high-speed processability becomes noticeable when the film is subjected to extrusion lamination processing, and the width and thickness of the resin film fluctuates, a so-called draw resonance phenomenon, which significantly reduces the commercial value. Lose.

かかる欠点を解消する手段として該ポリエチレンに高圧
法低密度ポリエチレンを配合することが扁られ、いる<
qe開昭58−194935号1%開昭58−1228
26号など〕。しかしながら、これらの手段によっても
前記欠点の改良は不十分である。
As a means to eliminate such drawbacks, it has been proposed to blend high-pressure low-density polyethylene into the polyethylene.
qe Kaisho 58-194935 No. 1% Kaisho 58-1228
26 etc.]. However, even with these measures, the above-mentioned drawbacks are not sufficiently improved.

、このような事情に鑑み、本発明者らは前記欠点を解消
したポリエチレン樹脂組成物を開発すべく検討を重ねた
結果、直鎖低密度ポリエチレンに高分子量の分率の大き
い高圧法低密度ポリエチレンを所定量配合した樹脂組成
物から得られるフィルムが高速加工性属すぐれ、かつヒ
ートシール強度等も良好であることを見出し、かかる知
見に基いて本発明を完成するに至った。
In view of these circumstances, the inventors of the present invention have conducted repeated studies to develop a polyethylene resin composition that eliminates the above-mentioned drawbacks. It has been discovered that a film obtained from a resin composition containing a predetermined amount of the following is excellent in high-speed processability and has good heat-sealing strength, etc., and based on this knowledge, the present invention has been completed.

すなわち本発明は、密度0.900〜0.9409/c
IIL” + メルトインデックス1〜25#/10分
のエチレン−α−オレフイン共重合体90〜50重量%
と、重量平均分子量(M、 )と数平均分子量(Mn)
の比My/MHが4〜15であり、重量平均分子量が5
万〜30万1分子量5万以上の分率が5〜24重量%で
ある高・圧法低密度ポリエチレン10〜50重量5より
なる低密度ポリエチレン樹脂組成物を提供するものであ
る。
That is, the present invention has a density of 0.900 to 0.9409/c
IIL" + 90-50% by weight of ethylene-α-olefin copolymer with melt index 1-25#/10 minutes
, weight average molecular weight (M, ) and number average molecular weight (Mn)
The ratio My/MH is 4 to 15, and the weight average molecular weight is 5.
The present invention provides a low density polyethylene resin composition comprising 10 to 50% by weight of high-pressure low density polyethylene having a molecular weight of 5 to 24% by weight.

本発明に用いるエチレン−α−オレフイン共重合体にお
けるα−オレフインとしては08〜CI。のもの、好ま
しくは04〜C8のα−オレフインであり、具体的には
プロピレン、1−ブテン、1−ペンテン、4−メチル−
ペンテン−1,1−ヘキセン、1−オクテン、l−デセ
ンなどがある。このエチレン−α−オレフイン共重合体
は密度9.900〜0.94011 /lx”、好まし
くは0.915〜0.9351/crXであり、メルト
インデックス(MI)1〜25g/10分、好ましくは
3〜1011710分のものを使用する。ここで密度(
JI8 K6760に準拠)が0.9001/cat”
未満であると、得られるフィルムのヒートシール強度が
低下し、また0、940g/aILaを超えると、フィ
ルムのホットタック性。
The α-olefin in the ethylene-α-olefin copolymer used in the present invention is 08 to CI. α-olefins, preferably 04 to C8, specifically propylene, 1-butene, 1-pentene, 4-methyl-
Examples include pentene-1,1-hexene, 1-octene, and l-decene. This ethylene-α-olefin copolymer has a density of 9.900 to 0.94011/lx", preferably 0.915 to 0.9351/crX, and a melt index (MI) of 1 to 25 g/10 min, preferably Use one with 3 to 1011710 minutes.Here, the density (
(based on JI8 K6760) is 0.9001/cat”
If it is less than 0.940g/aILa, the heat sealing strength of the resulting film will be reduced, and if it exceeds 0.940g/aILa, the hot tackiness of the film will be reduced.

透明性などが不良となり好ましくない。MI(JISK
6760に準拠)が19710分未満のものは、流動性
に劣り、しかも臨界加工速度力【低く、生産性の劣るも
のとなり、25 F/10分を超えたものは、フィルム
のヒートシール強度が不足する。
This is not preferable because it results in poor transparency. MI(JISK)
6760) for less than 19710 minutes will result in poor fluidity and low critical processing speed force, resulting in poor productivity; if it exceeds 25 F/10 minutes, the heat sealing strength of the film will be insufficient. do.

次に、高圧法低密度ポリエチレンは、前述したようにl
&/Mnが4〜15のもの、好ましくは8〜12のもの
である。ここで、分子量分布(′¥’h/′□)の測定
は、ウォーターズ社製1500(カラム:ムD80M 
X 2本、ムD807X2本、溶媒:オルトジクロルベ
ンゼン、温度:135℃、流量: l d/min )
を用いるGPO法により行ない、この比が4未満である
と、上記エチレン−α−オレフイン共重合体に配合する
効果が少なく、臨界加工速度の上昇が小さいため、生産
性の向上が不十分である。一方、比が15を超えると、
ドローダウン性(高速引取性)が悪くなり、フィルムが
製造できなくなる。
Next, as mentioned above, the high-pressure low-density polyethylene
&/Mn is from 4 to 15, preferably from 8 to 12. Here, the molecular weight distribution ('\'h/'□) was measured using Waters Co., Ltd. 1500 (column: MuD80M).
x 2, Mu D807 x 2, solvent: orthodichlorobenzene, temperature: 135°C, flow rate: l d/min)
If this ratio is less than 4, the effect of blending into the ethylene-α-olefin copolymer will be small, and the increase in critical processing speed will be small, resulting in insufficient improvement in productivity. . On the other hand, when the ratio exceeds 15,
Drawdown properties (high-speed take-up properties) deteriorate, making it impossible to produce a film.

また、このポリエチレンはMw 、すなわち重量平均分
子量は5万〜30万、好ましくは10万〜20万であり
、かつ分子量5万以上の分率が5〜24重量%、好まし
くは9〜18重量うのものを使用する。ここで−が5万
未満であると、上記エチレン−α−オレフイン共重合体
への配゛合効果が少なく、臨界加工速度の上昇が小さい
ため、生産性の向上が不十分である。また、MYが30
万を超えると、ドローダウン性が向上しないため、フィ
ルムの製造が不可能となる。分子量5万以上の分率が5
重量5未満であると、配合したことによる臨−界加2工
速度の上昇が小さく、生産性が向上しない。
Further, this polyethylene has a Mw, that is, a weight average molecular weight of 50,000 to 300,000, preferably 100,000 to 200,000, and a fraction of molecular weight of 50,000 or more is 5 to 24% by weight, preferably 9 to 18% by weight. Use the one. If - is less than 50,000, the effect of incorporation into the ethylene-α-olefin copolymer is small and the increase in critical processing speed is small, resulting in insufficient improvement in productivity. Also, MY is 30
If it exceeds 10,000, the drawdown properties will not improve, making it impossible to manufacture the film. The fraction with a molecular weight of 50,000 or more is 5
If the weight is less than 5, the increase in critical machining speed due to blending will be small and productivity will not improve.

一方、24重量5を超えると、ドローダウン性が悪くな
り、フィルムの製造が不可能となる。
On the other hand, if it exceeds 24% by weight, the drawdown properties will deteriorate, making it impossible to produce a film.

本発明の樹脂組成物において、エチレン−α−オレフイ
ン共重合体と高圧法低密度ポリエチレンの配合割合は前
者90〜50重量%、好ましくは85〜70重量%に対
して後者10〜50重量%、好ましくは15〜30重量
%とすべきである。エチレン−α−オレフイン共重合体
の配合割合が90重重量上超えると、臨界加工速度が低
下し、生産性は向上せず、押出ラミネート加工性が改良
されない。一方、該共重合体の配合割合が50重量5未
満であると、押出コーティングした積層フィルムの機械
的強度やヒートシール性の改良が不十分であり、たとえ
ば水物包装のような大きい包装材料としての用途に不適
当なものとなる。。
In the resin composition of the present invention, the blending ratio of the ethylene-α-olefin copolymer and high-pressure low density polyethylene is 90 to 50% by weight, preferably 85 to 70% by weight of the former, and 10 to 50% by weight of the latter. Preferably it should be between 15 and 30% by weight. If the blending ratio of the ethylene-α-olefin copolymer exceeds 90% by weight, the critical processing speed will decrease, productivity will not improve, and extrusion lamination processability will not be improved. On the other hand, if the blending ratio of the copolymer is less than 50% by weight, the mechanical strength and heat sealability of the extrusion-coated laminated film will not be sufficiently improved, and it will not be suitable for use as a large packaging material such as packaging for water products. becomes unsuitable for this purpose. .

本発明の樹脂組成物には上記成分のはか、使用目的など
を考慮して紫外線吸収剤、熱安定剤、帯電防止剤、酸化
防止剤、光安定剤、核剤なとの各種添加剤を適宜加える
ことができる。
The resin composition of the present invention contains various additives such as ultraviolet absorbers, heat stabilizers, antistatic agents, antioxidants, light stabilizers, and nucleating agents, taking into consideration the properties of the above components and the purpose of use. Can be added as appropriate.

本発明の樹脂組成物は、上記各成分を所定量配合し、た
とえば乾湿・融混併用法、多段溶融混合法、単純溶融混
合法等により十分に混練することによって得ることがで
きる。なお、混線はバンバリーミキサ−、コニーダー、
押出機、二軸混練機等を使用して行なうことができる。
The resin composition of the present invention can be obtained by blending the above-mentioned components in predetermined amounts and thoroughly kneading the mixture by, for example, a dry-wet/melt-mixing method, a multistage melt-mixing method, a simple melt-mixing method, or the like. In addition, the crosstalk is Banbury mixer, co-kneader,
This can be carried out using an extruder, a twin-screw kneader, or the like.

このようにして得られた本発明の樹脂組成物は、直鎖低
密度ポリエチレンフィルムの欠点とされていた臨界加工
速度が改善され、生産上の向上が著しい上に、該フィル
ムが本来的に有している優れたヒートシール強度、夾維
物シール強度、ホットタック性を保持している。そのた
め、押出2ミネート加工や包装用資材(特に食品包装用
資材)として極めて有用である。
The thus obtained resin composition of the present invention improves the critical processing speed, which has been considered a drawback of linear low-density polyethylene films, and not only significantly improves productivity, but also It has excellent heat seal strength, fiber seal strength, and hot tack properties. Therefore, it is extremely useful for extrusion lamination processing and packaging materials (particularly food packaging materials).

次に、本発明の実施例を示す。Next, examples of the present invention will be shown.

実施例1〜7 表に示すエチレン−α−オレフイン共重合体と高圧法低
密度ポリエチレンをVブレンダーで混合したのち一軸押
出機で溶融混練しながらT−ダイスから押出して成膜し
た。なお、T−ダイスはリップ開口長470wn。スリ
ット幅0.7簡のストレートマニホールドタイプを用い
た。
Examples 1 to 7 The ethylene-α-olefin copolymer and high-pressure low-density polyethylene shown in the table were mixed in a V-blender, and then extruded from a T-die while being melt-kneaded in a single-screw extruder to form a film. Note that the T-die has a lip opening length of 470wn. A straight manifold type with a slit width of 0.7 mm was used.

次に、厚さ15μの延伸ナイロンに厚さ20μの低密度
ポリエチレンを押出してコートしたものを基材とし、こ
れに上記組成物からなるフィルムを押出しラミネート加
工を行ない、臨界加工速度を測定した。また、上記フィ
ルムの厚みが30μとなる加工速度で押出コーティング
してラミネートフィルムを得た。得られたラミネートフ
イルムノヒートシール強度、夾緒物シール強度およびホ
ットタック性を測定した。結果を表に示す。
Next, a 15 μm thick stretched nylon extruded and coated with 20 μm thick low density polyethylene was used as a base material, and a film made of the above composition was extruded and laminated thereon, and the critical processing speed was measured. Further, a laminate film was obtained by extrusion coating at a processing speed such that the thickness of the film was 30 μm. The heat seal strength, impurity seal strength, and hot tack property of the obtained laminate film were measured. The results are shown in the table.

比較例1〜3 表に示す高圧法低密度ポリエチレンの単独フィルムを実
施例と同一装置および条件で押出ラミネート加工を行な
った。結果を表に示す。
Comparative Examples 1 to 3 Single films of high-pressure low-density polyethylene shown in the table were subjected to extrusion lamination using the same equipment and conditions as in Examples. The results are shown in the table.

比較例4.5 表ニ示すエチレン−α−オレフイン共重合体の単独フィ
ルムを実施例と同一装置および条件で押出ラミネート加
工を行なった。しかし、加工は不安定で臨界加工速度も
遅く、臨界加工速度を越えると、コート幅、コート厚み
の変動が大きく、押出ラミネート製品として商品価値の
ないものしか得られなかった。
Comparative Example 4.5 A single film of the ethylene-α-olefin copolymer shown in Table 2 was extrusion laminated using the same equipment and conditions as in Example. However, the processing is unstable and the critical processing speed is slow, and when the critical processing speed is exceeded, the coating width and coating thickness fluctuate greatly, and only extrusion laminate products with no commercial value can be obtained.

比較例6,7 エチレン−α−オレフイン共重合体と高圧法低密度ポリ
エチレンの配合割合を変えたこと以外は実施例と同様に
行なった。この場合、臨界加工速度はある程度上昇する
が、十分でなく押出ラミネート製品として商品価値のな
いものしか得られなかった。
Comparative Examples 6 and 7 The same procedure as in Example was carried out except that the blending ratio of the ethylene-α-olefin copolymer and the high-pressure low-density polyethylene was changed. In this case, although the critical processing speed increases to some extent, it is not sufficient and only extrusion laminate products with no commercial value can be obtained.

比較例8〜11 表に示したエチレン−α−オレフイン共重合体と高圧法
低密度ポリエチレンの組成物のフィルムを実施例と同一
装置および条件で押出ラミネート加工を行なった。この
場合も、臨界加工速度はある程度上昇するが、十分でな
く、押出ラミネート製品として商品価値のないものしか
得られなかった。
Comparative Examples 8 to 11 Films of the compositions of the ethylene-α-olefin copolymer and high-pressure low-density polyethylene shown in the table were extrusion laminated using the same equipment and conditions as in the examples. In this case as well, although the critical processing speed was increased to some extent, it was not sufficient and only extrusion laminate products with no commercial value were obtained.

*1エチレンーα−オレフイン共j1体A:エチレン−
オクテン−1共重合体(密度0.920 g/arr”
 、 XI 4.09/x o分)B:エチレン−ブテ
ン−1共重合体 (密度0.92311/値s、 MI
 +、Og/l、o分)*2高圧法低密度ポリエチレン a:  10.5  20万  17   0.910
  8.0k):   7.0  15万  15  
 0.915  7.5C:   5.2  14万 
 13  0.923  6.3(i:   3.5 
 9万   5   0.918  25.Oe:  
16.0  18万  15   0.920  2.
0f:   6.0  4万   6   0.917
  4.7g:   5.5  11万   4  0
.919  4.5*3臨界加工速度 ドローレゾナンスが生じる加工速度をいい、実生産機で
は1507FL/分以上の加工速度が要求される。ドロ
ーレゾナンスとは、ある加工速度を超えるとフィルムの
幅や肉厚が変動し、ムラが発生する現象をいう。
*1 Ethylene-α-olefin coj1 body A: Ethylene-
Octene-1 copolymer (density 0.920 g/arr"
, XI 4.09/x o min) B: Ethylene-butene-1 copolymer (density 0.92311/value s, MI
+, Og/l, o min) *2 High pressure low density polyethylene a: 10.5 200,000 17 0.910
8.0k): 7.0 150,000 15
0.915 7.5C: 5.2 140,000
13 0.923 6.3 (i: 3.5
90,000 5 0.918 25. Oe:
16.0 180,000 15 0.920 2.
0f: 6.0 40,000 6 0.917
4.7g: 5.5 110,000 4 0
.. 919 4.5*3 Critical machining speed Refers to the machining speed at which draw resonance occurs, and a machining speed of 1507 FL/min or higher is required for actual production machines. Draw resonance is a phenomenon in which the width and thickness of the film fluctuate and unevenness occurs when the processing speed exceeds a certain level.

*4ヒートシール強度 東洋精機製の熱傾斜のヒートシーラ°−でシールした2
ミネートフイルムのヒートシール強度を示す。なお、ヒ
ートシール圧力2に9/α21時間1.θ秒でヒー“ト
シールした後、幅25m、引取速度200IIV′分で
測定した。
*4 Heat seal strength 2 Sealed with Toyo Seiki's heat-gradient heat sealer °-
The heat seal strength of the laminated film is shown. In addition, the heat sealing pressure 2 is 9/α21 hours 1. After heat sealing for θ seconds, measurements were taken at a width of 25 m and a take-up speed of 200 IIV' minutes.

*5夾雑物シール強度 ヒートシール面前が内容物、例えばマヨネーズ、食用油
、粉末等で汚染された場合のヒートシール性を評価する
方法であり、具体的にはサラダ油で汚染されたフィルム
面が内側になるように重ねてヒートシール強度の試験と
同一の条件でヒートシールした後、強度を求めた。
*5 Contaminant sealing strength This is a method to evaluate heat sealability when the front of the heat sealing surface is contaminated with contents, such as mayonnaise, edible oil, powder, etc. Specifically, the film surface contaminated with salad oil is on the inside. After heat-sealing them under the same conditions as the heat-sealing strength test, the strength was determined.

*6ホツトタツク性 2枚の積層フィルムの一端をヒートシーラーの上部つか
み具に固定し、他端に31gの錘をつけ、このフィルム
同士をヒートシールした後、シールバーが離れると同時
にシール部に錘による剥離力が働くようにし、シール部
の剥離長さを測定した(フィルム試料の幅15B)。
*6 Hot-tack property Fix one end of the two laminated films to the upper grip of the heat sealer, attach a 31g weight to the other end, heat seal the films together, and as soon as the seal bar separates, attach the weight to the sealing part. The peeling force was applied to the film, and the peeling length of the sealed portion was measured (width 15B of the film sample).

Claims (1)

【特許請求の範囲】[Claims] 密度0.900〜0.940g/cm^3、メルトイン
デツクス1〜25g/10分のエチレン−α−オレフイ
ン共重合体90〜50重量%と、重量平均分子量(@M
@w)と数平均分子量(@M@n)の比@M@w/@M
@nが4〜15であり、重量平均分子量が5万〜30万
、分子量5万以上の分率が5〜24重量%である高圧法
低密度ポリエチレン10〜50重量%よりなる低密度ポ
リエチレン樹脂組成物。
90 to 50% by weight of an ethylene-α-olefin copolymer with a density of 0.900 to 0.940 g/cm^3, a melt index of 1 to 25 g/10 minutes, and a weight average molecular weight (@M
@w) and number average molecular weight (@M@n) ratio @M@w/@M
A low-density polyethylene resin consisting of 10-50% by weight of high-pressure low-density polyethylene in which @n is 4 to 15, the weight average molecular weight is 50,000 to 300,000, and the fraction of molecular weight of 50,000 or more is 5 to 24% by weight. Composition.
JP14931484A 1984-07-20 1984-07-20 Low-density polyethylene resin composition Granted JPS6128538A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14931484A JPS6128538A (en) 1984-07-20 1984-07-20 Low-density polyethylene resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14931484A JPS6128538A (en) 1984-07-20 1984-07-20 Low-density polyethylene resin composition

Publications (2)

Publication Number Publication Date
JPS6128538A true JPS6128538A (en) 1986-02-08
JPH0430420B2 JPH0430420B2 (en) 1992-05-21

Family

ID=15472412

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14931484A Granted JPS6128538A (en) 1984-07-20 1984-07-20 Low-density polyethylene resin composition

Country Status (1)

Country Link
JP (1) JPS6128538A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5376439A (en) * 1992-09-16 1994-12-27 Exxon Chemical Patents Inc. Soft films having enhanced physical properties
US5594071A (en) * 1992-06-17 1997-01-14 Mitsui Petrochemical Industries, Ltd. Ethylene copolymer composition
US5663236A (en) * 1992-11-19 1997-09-02 Mitsui Petrochemical Industries, Ltd. Ethylene copolymer composition
US5863665A (en) * 1991-10-15 1999-01-26 The Dow Chemical Company Extrusion compositions having high drawdown and substantially reduced neck-in
US5904964A (en) * 1989-12-18 1999-05-18 E. I. Du Pont De Nemours And Company Process for manufacturing heat-shrinkable polyethylene film
US6774190B1 (en) 1992-06-17 2004-08-10 Mitsui Chemicals, Inc. Ethylene copolymer composition

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5904964A (en) * 1989-12-18 1999-05-18 E. I. Du Pont De Nemours And Company Process for manufacturing heat-shrinkable polyethylene film
US5863665A (en) * 1991-10-15 1999-01-26 The Dow Chemical Company Extrusion compositions having high drawdown and substantially reduced neck-in
US5594071A (en) * 1992-06-17 1997-01-14 Mitsui Petrochemical Industries, Ltd. Ethylene copolymer composition
US5674945A (en) * 1992-06-17 1997-10-07 Mitsui Petrochemical Industries, Ltd. Ethylene copolymer composition
US6774190B1 (en) 1992-06-17 2004-08-10 Mitsui Chemicals, Inc. Ethylene copolymer composition
US5376439A (en) * 1992-09-16 1994-12-27 Exxon Chemical Patents Inc. Soft films having enhanced physical properties
US5663236A (en) * 1992-11-19 1997-09-02 Mitsui Petrochemical Industries, Ltd. Ethylene copolymer composition
US6184297B1 (en) 1992-11-19 2001-02-06 Mitsui Chemicals Inc Ethylene copolymer composition
US6333387B1 (en) 1992-11-19 2001-12-25 Mitsui Chemicals Inc. Ethylene copolymer composition

Also Published As

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