JPS59192534A - Polyethylene stretched shape - Google Patents

Polyethylene stretched shape

Info

Publication number
JPS59192534A
JPS59192534A JP58196917A JP19691783A JPS59192534A JP S59192534 A JPS59192534 A JP S59192534A JP 58196917 A JP58196917 A JP 58196917A JP 19691783 A JP19691783 A JP 19691783A JP S59192534 A JPS59192534 A JP S59192534A
Authority
JP
Japan
Prior art keywords
molecular weight
polymer
average molecular
polyethylene
modulus
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
JP58196917A
Other languages
Japanese (ja)
Other versions
JPS6216813B2 (en
Inventor
イ−アン・マクミラン・ウオアルド
ジアンカルロ・カパシオ
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.)
National Research Development Corp of India
Original Assignee
National Research Development Corp of India
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 National Research Development Corp of India filed Critical National Research Development Corp of India
Publication of JPS59192534A publication Critical patent/JPS59192534A/en
Publication of JPS6216813B2 publication Critical patent/JPS6216813B2/ja
Granted legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/04Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (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】 本発明は新規制分子物質に関する。[Detailed description of the invention] The present invention relates to new regulated molecular substances.

物理的性質に改良を7111えた工業製品の出現はたえ
ず要求されているところであり、例えば最近炭素繊維に
対し非常に多くの関・しが寄ぜられている。
There is a constant demand for industrial products with improved physical properties, and for example, carbon fibers have received a great deal of attention recently.

次系繊維は非常に高い弾性率(4,2X 1011 N
/m2)iもっているが非常に高価であってその応用に
限界かめる。従来法によシポリエチレンのようなポリマ
ーから形成された繊aは廉価であるが弾性率に3いて劣
っている(約0.5〜0.7 X 101ON/m2)
The secondary fiber has a very high elastic modulus (4,2X 1011 N
/m2)i, but it is very expensive and there are limits to its application. Fibers a formed from polymers such as polyethylene by conventional methods are inexpensive but have an inferior modulus of elasticity of 3 (approximately 0.5 to 0.7 x 101 ON/m2).
.

本発明は上記物理的性質を改良した新規制分子物質成形
体を提供する。
The present invention provides a molded article of a new controlled molecular substance with improved physical properties.

すなわち、本発明はポリエチレンポリマー物質でろって
、重量平均分子量が200,000より小、数平均分子
量が20,000よシ小、重重平均分子量MWの数平均
分子量Mnに対する比率がM n )104のと^i 
w / M n < 10であって1n(104のとき
M w / M n (2Qでめム後に定義するヤング
率が3×101ON/m2 よシ大でめる配向性尚密度
ポリエチレン延伸成形俸を供する。
That is, the present invention provides a polyethylene polymer material having a weight average molecular weight of less than 200,000, a number average molecular weight of less than 20,000, and a ratio of weight average molecular weight MW to number average molecular weight Mn of 104. and ^i
When w / M n < 10 and 1n (104, then M w / M n (The Young's modulus defined after measurement in 2Q is greater than 3 × 101 ON/m2). provide

不明11書に2いて、毘密度ポリエチレンポリマーとは
、FJ95n貫%以上のエチレンを含む本質的に直鎮の
エチレンホモポリマーlたはコポリマーであって、「ブ
リティッシュ・スタンダード・スベシフイケーション蔦
3412(1966)アペンディックスA、[1)ff
aされ、同アペンディックスB(1)によりアニー/L
/されたサンプル(たとえば遷移金属触媒の存在下にエ
チレンを重合させて得られた生成物)葡ブリティッシュ
・スタンダード・スベシフイケーションA、’ 278
2 (1970)メソッド509Bの方法により、泪リ
ボしたときのff1pEi0.85〜1.OV/1yy
t3(Dモ(Dk云’)。」好1しくば、該ポリマーは
毎分約2〜10℃の速度で、約100〜120″Cfで
冷却した後、通常低温1で急冷する。連続操作に2いて
ほこの急3.      冷工程を省略して、保冷工程
後だ!゛ちに延伸ケ行なってもよい。
2 in Unknown 11, the term "polyethylene polymer per unit density" refers to an essentially straight-line ethylene homopolymer or copolymer containing ethylene of 95% or more by FJ, and is defined as "British Standard Subasification Ivy 3412". 1966) Appendix A, [1) ff
a, and according to the same appendix B(1) Annie/L
British Standard Subscription A, '278
2 (1970) method 509B, ff1pEi0.85 to 1. OV/1yy
t3 (Dk云'). Preferably, the polymer is cooled at a rate of about 2-10°C per minute to about 100-120"Cf, followed by quenching, usually at a low temperature 1. Continuous operation. 3. You may omit the cooling step and perform the stretching immediately after the cold storage step.

1だ、好1しくは、該ポリマーは車量平均分子重(倉W
 ) 50.000から150,0uOOものがよい。
1, preferably the polymer has a weight average molecular weight (W)
) 50,000 to 150,0uOO is good.

数平均分子量(Mn)は、5,000から15.000
が好ましい。更に重量平均分子姐の数平均分子量に対す
る劃8は約18以下が好葦しい。
Number average molecular weight (Mn) is 5,000 to 15,000
is preferred. Further, the ratio of the weight average molecular weight to the number average molecular weight is preferably about 18 or less.

特に分子量分4コ−が比較的狭いポリマー、即ちMn〉
104のと@ M w / M n < 6、Mn<1
04のとさMw/Mn(15であるようなものを用いる
と良い結果が得られる。なお、木明創書中に引)1」さ
れている分子量は、ゲル濾過クロマトグラフィーによっ
て測定したものである。
In particular, polymers with a relatively narrow molecular weight of 4 co-, that is, Mn>
104 and @ M w / M n < 6, M n < 1
Good results can be obtained by using a compound with a height Mw/Mn of 04 (15).The molecular weight indicated in ``1'' (quoted in Kimei Sosho) was measured by gel filtration chromatography. be.

本発明は、特定の理論によって限定されるものではない
が、所要の形態を有するポリマーをプラスチック変形工
程に付することにより、誦い配向度のポリマー分子か得
られるものと考えられる。
Although the present invention is not limited by any particular theory, it is believed that polymer molecules having a desired degree of orientation can be obtained by subjecting a polymer having a desired morphology to a plastic deformation process.

特に好ましいプラスチックの変形工程は、ポリマーを延
伸比少なくとも15、好互しくに少なくとも約20とな
るように延伸することから成る。もちろん延伸張力がポ
リマーの抗張力よりは小さいが、ポリマーの伸長がフロ
ー延伸によって生ずるであろう伸長以上のものでるって
必要な配回を生ずるに充分であるよりな速度と温度のも
とて延伸されることが必要でりる。処伸温)iはポリマ
ーの―点より少なくとも約40℃低いのが好ましい。
A particularly preferred plastic deformation process consists of stretching the polymer to a stretch ratio of at least 15, preferably at least about 20. Of course, the stretching tension is less than the tensile strength of the polymer, but the elongation of the polymer is greater than that which would occur by flow stretching, which is sufficient to produce the necessary alignment. It is necessary to do so. Preferably, the processing elongation temperature) i is at least about 40°C below the - point of the polymer.

延伸速度に、延伸l都度とポリマーの形態にもよるが、
通常回分11711以上、例えば毎分子J10〜20m
もしくはそれ以上でめっでもよい。好Iしくは、延伸温
度は約60〜90℃でめり、延伸比は少なくとも18、
望互しくに酌25〜60である。
It depends on the stretching speed, each stretching time, and the form of the polymer.
Usually 11,711 or more batches, for example J10-20m per molecule
Or even more than that. Preferably, the stretching temperature is about 60-90°C, the stretching ratio is at least 18,
The desired value is 25 to 60.

このポリマーの物理的性質は、増進期に延伸全遂行し、
継続期の間で休止させることによってしばしば改良され
ることかめる。
The physical properties of this polymer are fully carried out during the expansion phase,
It can often be improved by pausing between periods.

延伸は比較的小さな断面葡もったポリマーについてこれ
を行なうのが好1しく、本発明は特に繊維やフィルムを
製造するのに好週でめる。特に、連続フィラメントは浴
融紡糸と延伸フレーム上に2ける延伸により製危するこ
とかでさる。便宜上繊維の直径又はフィルムの厚さは延
伸@tJ vc2いて1朋以下が好ましい。
Stretching is preferably carried out on polymers with relatively small cross-sections, and the present invention is particularly suitable for producing fibers and films. In particular, continuous filaments are susceptible to production by bath melt spinning and drawing on a drawing frame. For convenience, the diameter of the fiber or the thickness of the film is preferably less than or equal to 1 mm in stretching@tJ vc2.

不明#I書における変形比又は延伸比は最初の長さに対
する最後の長さの比率又は延伸前後の@面積の比として
定杖される。
The deformation ratio or stretching ratio in Unknown #I is defined as the ratio of the final length to the initial length or the ratio of the area before and after stretching.

本発明方法によれは、ヤング率(後にボ義する)が3×
101ON/m2以上、場合VCヨッテVl 少なくと
も6 X 101ON1m2のポリマーを得ることがで
きる。超分子物質のヤング率は測定法に依存する面があ
るので、この明細書では、ヤング率とは、デツドーロデ
イングクリープ試験により21℃で01%のヂみを10
秒間維持してその応力を測定したときの弾性率と足義す
る。この試験法は、グプタおよびワード:ジャーナル・
オブ・マクロモレキュラー・サイエンヌ・アンド・フイ
ジクスB1.373(1967)に記載されている。
According to the method of the present invention, Young's modulus (defined later) is 3×
101 ON/m2 or more, if VC Yotte Vl at least 6 X 101 ON1 m2 of polymer can be obtained. Since the Young's modulus of supramolecular substances depends on the measurement method, in this specification, the Young's modulus is defined as the deviation of 0.1% at 21°C by the Detsudo Roding creep test.
The elastic modulus when the stress is measured by maintaining it for a second is defined as the foot. This test method was developed by Gupta and Ward: Journal
of Macromolecular Science and Physics B1.373 (1967).

本発明方法によれば、ポリマー分子はプラスチック変形
によって本質的に完全な直線状に配向する。一般に分子
配向は一軸的でるるが、適当な延伸方法を採用すること
によりニ軸的に配向した高分子物質ケ得ることも可能で
める。本質的に完全な配向性の存在は、物理的な測定法
例えはX線回折法又は核1磁気共鳴法によって確認する
ことができる。簡単な試験に、発煙硝酸中でポリマーの
減量k TAU定することによって行なわれ、これは誦
分子の児全1生を61リボするものでりる。減量が少な
ければ商い完余1生r勺すめことt怠1禾する。
According to the method of the invention, polymer molecules are oriented in essentially perfect straight lines by plastic deformation. Although molecular orientation is generally uniaxial, it is also possible to obtain a biaxially oriented polymer material by employing an appropriate stretching method. The presence of essentially perfect orientation can be confirmed by physical measurements such as X-ray diffraction or nuclear 1 magnetic resonance. A simple test is performed by determining the weight loss of the polymer in fuming nitric acid, kTAU, which is 61 ribs over the entire life of the molecule. If the weight loss is small, the trade will be completed in one lifetime.

本発明によるポリエチレンポリマーは、X線回折や核1
み気共鳴で観察され得ろごとく商い配向1生の悄造を有
している。特に、5 X 101ON/m2以」二の弾
1生率ff:狩つ試料は、発プ票イ萌r投甲に60℃で
10日間保存しでも重量減少4(は5%以F″′cメる
The polyethylene polymer according to the present invention can be
It has a unique structure in the direction of energy, which is observed in the miraculous resonance. In particular, samples with a bullet survival rate of 5 x 101 ON/m2 or more have a weight loss of 5% or more even when stored for 10 days at 60°C. C mail.

ポリエチレンのヤング率の1!li論jtU 24 X
l0ION / m 2であり、この発明によ!、I侍
られるポリマーがこの数組に非當に嵌通したヤング率を
有しているこち〃・わ〃・ろ。このラロ明VcLつて4
 X 101ON/m2 以上のヤング率、メしはしは
5〜7X101ON/m2の範囲のヤンク李盆もったポ
リエチレン全侶ることかでさる。
Young's modulus of polyethylene is 1! li theory jtU 24 X
10ION/m2, and according to this invention! , the polymer being used has a Young's modulus that does not quite fit into this set. This Lalo Akira VcL 4
Young's modulus of 101ON/m2 or more is suitable for all polyethylene materials with a Young's modulus of 5 to 7101ON/m2.

この発明によるポリエチレンポリマーは、結合」二車−
性のめる栴i’aヶ狩った形で得ることかでさゝ・λ る。それらはM丈でイhIIけ煤い。IIA」えはポリ
エチレン繊維は少なくとも7%の伸展性を有しており、
ファイバー状にすることかでさる。
The polyethylene polymer according to the present invention has a bond between two wheels.
Is it possible to obtain it by hunting it down? They are medium length and very sooty. The polyethylene fiber has an extensibility of at least 7%,
It depends on how it is made into fibers.

次の実施例でこの発明を更に詳細に説明する。The invention will be explained in further detail in the following examples.

実施例1 直径Q、ldmのダイを通し、190℃で俗調紡糸する
ことによV直径006〜007mのアイソトロピツクフ
ィラメントヲ得る。このフイラメン)′fr:23r、
P、m、  の速度で回転する石住5.5 Cnrのシ
リング゛−に巻きとる。該ポリマーの冷却速度全毎分5
℃に調整し、その温度が115℃に達したとき生ずる栴
倉を急冷して保持する。畏さ3〜4αの試料ケインスト
ロン引張試験機音用いて72℃で30〜45秒間クロス
ヘッド速度母分20Crnの条件のもとに延伸する。延
伸比にフィラメント断面の変動をもとに決定する。
Example 1 An isotropic filament with a V diameter of 006 to 007 m was obtained by spinning at 190° C. through a die with a diameter of Q and ldm. This filamen)'fr:23r,
It is wound around a 5.5 Cnr cylinder rotating at a speed of P, m, . The total cooling rate of the polymer is 5 per minute.
℃, and when the temperature reaches 115°C, the resulting coolant is rapidly cooled and held. A sample having a strength of 3 to 4α is stretched using a Kanestron tensile tester at 72° C. for 30 to 45 seconds at a crosshead speed of 20 Crn. The drawing ratio is determined based on the variation of the filament cross section.

試料として市販のビー・ビー(BP)高品度ポリエチレ
ンから選んだ二種類のポリマーを使用する。一つは07
5−60グレード、温度190℃νよび荷M2.14即
で測定したときのメルトフロ9.100でめる。他は、
リジテ゛ツクス(Rigidex9)で、ノルドフロー
インデックスQ、9.Mn:6060、 Ivlw: 
126,600でりる。10秒ヤング李を¥篩(21℃
)で關足する。075−60クレードは、狭い分子量分
伸すなわち1すw 7M n−48,延伸に:20.ヤ
ンク李4.0XIOION/ m 2の延伸j戊形秤が
侍られる。一方すシデツクス9ハ111If1広い分子
量分伸すなわちM w / M n = 209と商い
東亜平均分子Mヶ有してとり、七の結果かなり低いヤン
グ率を有する延伸成形坏が侍られる。上d己の来町の連
続フィラメントは延伸フレーム上で延伸されることVC
より同様の帖朱奮与える。
Two types of polymers selected from commercially available BP high-grade polyethylene are used as samples. One is 07
5-60 grade, with a melt flow of 9.100 when measured at a temperature of 190°C v and a load of M2.14. Others are
Rigidix (Rigidex9), Nord flow index Q, 9. Mn:6060, Ivlw:
It costs 126,600. Sieve the young lily for 10 seconds (21℃
). The 075-60 clade has a narrow molecular weight range: 1 w 7M n-48, 20. A Yank Li 4.0XIOION/m2 extended hollow scale is used. On the other hand, when Sidex 9 has a wide molecular weight distribution, ie, Mw/Mn=209, and has an average molecular weight of M, a stretch-formed material having a considerably low Young's modulus is obtained. The continuous filament of the upper part is drawn on a drawing frame VC
Give more similar chapters.

実施例2 品雷反ポリエチレン々レット紫二我の銅板の間で160
℃に2いて圧顛成形することにより0.05〜007m
厚のシート紫得る。このシート’7ブレヌからとVはつ
し、毎分7〜9℃の割合でゆつ<v100℃1で冷却し
く綱板の表囲で7則足する。
Example 2 160 between anti-polyethylene and purple copper plates
0.05~007m by pressing at 2°C
Get thick sheets purple. From this sheet '7 Blaine, V is cut and cooled at a rate of 7 to 9 degrees Celsius per minute < v100 degrees Celsius, and 7 rules are added to the surface area of the steel plate.

)、次いで冷水中に人nて恕節する。長さ2t7n、1
当υ5C/#の長万形試f4奮インストロン引張試験機
葡用いて、75℃に2いてクロスヘッド運度旬:分10
(7)で70〜90秒間延伸する。延伸J:JSは延伸
mtJの試料の表面に0.2又は0.11の間隔で印を
つけそれによって測定する。
), then place the person in cold water and pray. Length 2t7n, 1
This υ5C/# long-shaped test F4 was carried out using an Instron tensile tester, heated to 75°C, and the crosshead movement was carried out for 10 minutes.
(7) Stretch for 70 to 90 seconds. Stretch J: JS is measured by marking the surface of the sample at an interval of 0.2 or 0.11 for the stretch mtJ.

試料として市販のビー・ビー(BP)高密度ポリエチレ
ンη)ら選んだ2種類のグレードのものを用いる。リシ
デツクヌ50はメルトフローインチ0でめり、140−
60グレードはノルドフローインテックス12.Mn:
13350.MW:[j7800でめる。リシテツクヌ
50についての最大延伸比は30.140−60グレー
ドについての最大延伸比は37〜38と泪IJ足さ扛る
Two grades of commercially available high-density polyethylene (BP) were used as samples. Rishidecukunu 50 is melt flow inch 0, 140-
60 grade is Nord Flow Intex 12. Mn:
13350. MW: [j7800. The maximum stretch ratio for Rishitetsukune 50 is 30. The maximum stretch ratio for 140-60 grade is 37-38, which is as low as IJ.

代表的な試料について室温でのlO抄ヤンク率全測定し
その結果を欠の表に示す。
The lO paper yank rate was completely measured at room temperature for a representative sample, and the results are shown in the table below.

入に不兄明の範囲に包含される技侑的惑株の具俸例葡挙
げる。
Let me give you an example of the amount of money that is included in the scope of the unbiased technique.

(1〕  車量平均分子重が201J、000より小、
数平均分子が20,000より小、車重平均分子MMW
の数平均分子量Mnに対する比率がM n ) l Q
4のときM w / M n (l Q、Mn<IQ4
のトサM w / M n (20でめムヤンク率が3
X、101ON/m2 より大でめる配向性品密度ポリ
エチレンポリマー。
(1) Vehicle weight average molecular weight is smaller than 201J, 000,
Number average molecule is less than 20,000, vehicle weight average molecule MMW
The ratio of M n ) l Q to the number average molecular weight Mn is
4, M w / M n (l Q, Mn<IQ4
Tosa M w / M n (memyank rate is 3 at 20
X, oriented product density polyethylene polymer that can be larger than 101 ON/m2.

(2)里量平均分子賞50,000〜150,000を
有する上a己(1)記載のポリエチレンポリマー。
(2) The polyethylene polymer according to (1) above, having an average molecular weight of 50,000 to 150,000.

(3〕  数平均分子量5,000〜15,000を有
する上記(1)又は(2)記載のポリエチレンポリマー
(3) The polyethylene polymer according to (1) or (2) above, having a number average molecular weight of 5,000 to 15,000.

ある上記(1)〜(3)記載のポリエチレンポリマー。A certain polyethylene polymer described in (1) to (3) above.

(5)  発煙硝酸中に60℃で10日間放直したとき
の車重減少率が7fJ5%以下である上記(1〕〜(4
)記載のポリエチレンポリマー。
(5) Vehicles listed in (1) to (4) above whose weight loss rate is 7fJ5% or less when left in fuming nitric acid at 60°C for 10 days.
) described polyethylene polymer.

(6)  −III111旧に配向した上記(1)〜(
5)記載のポリエチレンポリマー。
(6) -III111 orientated above (1) to (
5) Polyethylene polymer as described.

(7〕  ファイバー又はフィルムでめる上記(x>〜
(6)記載のポリエチレンポリマー。
(7) The above (x>~
(6) The polyethylene polymer described.

(8)連続的フィラメントでめる上記(1)〜(7)記
載のポリエチレンポリマー。
(8) The polyethylene polymer described in (1) to (7) above, which is formed of continuous filaments.

手続補正書(自発) 昭和58年11月18日 j 特許庁長官 殿       1.1.自1 事件の表
示 昭和58年特許願第  196917   号2発明の
名称 ポリエチレン延伸成形体 3補正をする者 事件との関係 特許出願人 国籍 イギリス国 4、代理人 5補正命令の日付 (自 発) 佃委用−年 7補正の内容 (1)明細書の「特許請求の範囲」の欄を別紙の通り訂
正する。
Procedural Amendment (Voluntary) November 18, 1980 j Dear Commissioner of the Patent Office 1.1. (1) Indication of the case: Patent Application No. 196917, filed in 1982 (2) Name of the invention: Polyethylene stretched molded article (3) Person making the amendment Relationship to the case: Patent applicant nationality: United Kingdom (4), Agent (5) Date of amendment order (voluntary) Tsukuda Commission - Contents of amendment in 2007 (1) The "Claims" column of the specification is corrected as shown in the attached sheet.

(2)明細書第2頁末第5行、r 20. OU Oj
とあるをr 25. OOOjに訂正する。
(2) Line 5 at the end of page 2 of the specification, r 20. OU Oj
A certain r 25. Corrected to OOOj.

(3)同第2頁末第3行、r<IOJとあるを[〈81
に訂正する。
(3) On the third line at the end of the second page, r<IOJ [<81
Correct.

(41同第4 頁第5行、rMn(10’Jとあるを「
M n (I O−lに訂正する。
(41, page 4, line 5, rMn (10'J)
M n (Corrected to I O-l.

(5)同第7頁末第9行、「こちが1とあるを「こ吉が
」に訂正する。
(5) In line 9 at the end of page 7, ``Kochiga 1'' is corrected to ``Kokichiga''.

柵委詳獣÷尋騰柑詞j燭HトlH傷I→七以   」ニ 〔別  紙〕 特許請求の範囲 1、重量平均分子量が200,000より小、数平均分
子量が25,000より小、重量平均分子量20であり
、ヤング率が3 X 101ON/rtfより大である
高密度ポリエチレン延伸成形体。
[Attachment] Claim 1: The weight average molecular weight is less than 200,000, and the number average molecular weight is less than 25,000. , a high-density polyethylene stretch molded body having a weight average molecular weight of 20 and a Young's modulus of greater than 3 x 101 ON/rtf.

Claims (1)

【特許請求の範囲】 1重量平均分子量が200,000より小、数平均分子
量が20.000より小、重量平均分子量Mwの数平均
分子量Mnに対する比率がMr+)IQ のときMw/
Mn<] O1Mn(IQ4のときM w / M n
<20であり、ヤング率が3×101ON/ゴであル高
密度ポリエチレン延伸成形体。 (以下、余白)
[Claims] When the weight average molecular weight is less than 200,000, the number average molecular weight is less than 20,000, and the ratio of the weight average molecular weight Mw to the number average molecular weight Mn is Mr+)IQ, Mw/
Mn<] O1Mn (M w / M n when IQ4
<20, and Young's modulus is 3×101 ON/g. High-density polyethylene stretched molded body. (Hereafter, margin)
JP58196917A 1973-03-06 1983-10-19 Polyethylene stretched shape Granted JPS59192534A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB1074673A GB1469526A (en) 1973-03-06 1973-03-06 Polymer materials
GB10746/73 1973-03-06

Publications (2)

Publication Number Publication Date
JPS59192534A true JPS59192534A (en) 1984-10-31
JPS6216813B2 JPS6216813B2 (en) 1987-04-14

Family

ID=9973530

Family Applications (2)

Application Number Title Priority Date Filing Date
JP49026705A Expired JPS5746414B2 (en) 1973-03-06 1974-03-06
JP58196917A Granted JPS59192534A (en) 1973-03-06 1983-10-19 Polyethylene stretched shape

Family Applications Before (1)

Application Number Title Priority Date Filing Date
JP49026705A Expired JPS5746414B2 (en) 1973-03-06 1974-03-06

Country Status (13)

Country Link
JP (2) JPS5746414B2 (en)
BE (1) BE811853A (en)
CA (1) CA1059278A (en)
CS (1) CS181752B2 (en)
DE (1) DE2410747C2 (en)
ES (1) ES423956A1 (en)
FR (1) FR2220547B1 (en)
GB (1) GB1469526A (en)
IE (1) IE39164B1 (en)
IT (1) IT1013059B (en)
LU (1) LU69546A1 (en)
NL (1) NL184696B (en)
ZA (1) ZA741145B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6472827A (en) * 1987-09-16 1989-03-17 Showa Denko Kk Polyethylenic film

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1506565A (en) * 1974-03-05 1978-04-05 Nat Res Dev Production of polyethylene filaments
GB1568964A (en) * 1975-11-05 1980-06-11 Nat Res Dev Oriented polymer materials
NL177759B (en) * 1979-06-27 1985-06-17 Stamicarbon METHOD OF MANUFACTURING A POLYTHYTHREAD, AND POLYTHYTHREAD THEREFORE OBTAINED
JPS5752403A (en) * 1980-09-11 1982-03-27 Kyoto Prefecture Production of fan stick
NL8104728A (en) * 1981-10-17 1983-05-16 Stamicarbon METHOD FOR MANUFACTURING POLYETHENE FILAMENTS WITH GREAT TENSILE STRENGTH
JPS59167649U (en) * 1983-05-04 1984-11-09 京都府 Fan rib manufacturing equipment
GB8404843D0 (en) * 1984-02-24 1984-03-28 Amersham Int Plc Free analyte assay
JPS61121867A (en) * 1984-11-20 1986-06-09 Masakatsu Hoshino Polishing method for both side surfaces of metal foreign-style tableware
JPH074752B2 (en) * 1987-01-29 1995-01-25 三菱重工業株式会社 6-axis control automatic polishing machine
US4882230A (en) * 1987-10-30 1989-11-21 Kimberly-Clark Corporation Multilayer polymeric film having dead bend characteristics
JPH0577855U (en) * 1992-03-23 1993-10-22 株式会社トータス Positioning of the circuit board to the leg of the image quality compensator Temporary fixing structure
US5549867A (en) * 1994-11-03 1996-08-27 Fiberweb North America, Inc. Distribution enhanced polyolefin meltspinning process and product
GB0128405D0 (en) * 2001-11-27 2002-01-16 Btg Int Ltd Process for fabricating polyolefin sheet

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6472827A (en) * 1987-09-16 1989-03-17 Showa Denko Kk Polyethylenic film

Also Published As

Publication number Publication date
IT1013059B (en) 1977-03-30
AU6593674A (en) 1975-08-28
NL7402956A (en) 1974-09-10
GB1469526A (en) 1977-04-06
CS181752B2 (en) 1978-03-31
LU69546A1 (en) 1974-06-21
NL184696B (en) 1989-05-01
CA1059278A (en) 1979-07-31
DE2410747A1 (en) 1974-09-12
FR2220547A1 (en) 1974-10-04
DE2410747C2 (en) 1983-02-10
JPS5025679A (en) 1975-03-18
IE39164B1 (en) 1978-08-16
IE39164L (en) 1974-09-06
ES423956A1 (en) 1976-11-01
JPS5746414B2 (en) 1982-10-02
FR2220547B1 (en) 1978-01-06
BE811853A (en) 1974-09-04
ZA741145B (en) 1975-01-29
JPS6216813B2 (en) 1987-04-14

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