JPH0673244A - Ethylene copolymer composition - Google Patents
Ethylene copolymer compositionInfo
- Publication number
- JPH0673244A JPH0673244A JP5024330A JP2433093A JPH0673244A JP H0673244 A JPH0673244 A JP H0673244A JP 5024330 A JP5024330 A JP 5024330A JP 2433093 A JP2433093 A JP 2433093A JP H0673244 A JPH0673244 A JP H0673244A
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- phosphite
- copolymer
- ethylene copolymer
- pipe
- 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
- 229920001038 ethylene copolymer Polymers 0.000 title claims abstract description 24
- 239000000203 mixture Substances 0.000 title claims description 14
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000005977 Ethylene Substances 0.000 claims abstract description 16
- 239000004711 α-olefin Substances 0.000 claims abstract description 14
- 229920001577 copolymer Polymers 0.000 claims abstract description 10
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims abstract description 9
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 7
- 239000000155 melt Substances 0.000 claims abstract description 5
- -1 2,4-di-t-butylphenyl Chemical group 0.000 claims description 13
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 7
- 229910000423 chromium oxide Inorganic materials 0.000 claims description 7
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- JBTXGEJRJCNRLU-UHFFFAOYSA-N [2-(dihydroxyphosphanyloxymethyl)-3-hydroxy-2-(hydroxymethyl)propyl] dihydrogen phosphite Chemical compound OP(O)OCC(CO)(CO)COP(O)O JBTXGEJRJCNRLU-UHFFFAOYSA-N 0.000 claims description 3
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims description 3
- GIATZHZBSIMOEE-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C Chemical compound P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C GIATZHZBSIMOEE-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 2
- CCULFEHGNPNAAT-UHFFFAOYSA-N C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C Chemical compound C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C CCULFEHGNPNAAT-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 26
- 238000000465 moulding Methods 0.000 abstract description 15
- 238000004513 sizing Methods 0.000 abstract description 10
- 230000037303 wrinkles Effects 0.000 abstract description 7
- 238000013329 compounding Methods 0.000 abstract description 3
- 239000011990 phillips catalyst Substances 0.000 abstract description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000011651 chromium Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 229920000573 polyethylene Polymers 0.000 description 8
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000011342 resin composition Substances 0.000 description 6
- 238000001125 extrusion Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 238000012690 ionic polymerization Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- RRFWWSOELBTKEK-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C(CCCCCCCCCCCCCCCCC)C(O)(C(CO)(CO)CO)CCCCCCCCCCCCCCCCCC Chemical compound P(O)(O)O.P(O)(O)O.C(CCCCCCCCCCCCCCCCC)C(O)(C(CO)(CO)CO)CCCCCCCCCCCCCCCCCC RRFWWSOELBTKEK-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000007613 slurry method Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- 241000156978 Erebia Species 0.000 description 1
- FRCLQKLLFQYUJJ-UHFFFAOYSA-N P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C Chemical compound P(O)(O)O.P(O)(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C FRCLQKLLFQYUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000010349 pulsation Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 230000037330 wrinkle prevention Effects 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Rigid Pipes And Flexible Pipes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、特に外径サイジング成
形法による厚肉パイプの成形材料に好適な、パイプの平
滑性に優れたエチレン共重合体組成物に関するものであ
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an ethylene copolymer composition excellent in smoothness of a pipe, which is particularly suitable as a molding material for a thick pipe by an outer diameter sizing molding method.
【0002】[0002]
【従来の技術】従来、ポリエチレン製パイプの成形法
は、ジョイント接続の施工上、パイプ寸法管理において
内径よりも外径の方が重要視されることから、外径サイ
ジング成形法を用い、また材料として、押出成形性の観
点より比較的分子量分布の広い汎用の押出成形用高密度
ポリエチレンおよび低密度ポリエチレンを使用するのが
一般的であった。ポリエチレン製パイプは長期性能、耐
薬品性に優れ、しかも安価で加工が容易であるため、そ
の特性を活かして古くから給排水管に主として用いられ
てきた。特に低密度のエチレン・α−オレフィン共重合
体(直鎖状低密度ポリエチレン)は柔軟性、耐塩素水性
等の優れた特徴を有していることから、JIS−K67
62の一種管(軟質管)にも近年使用されだしている。
また、外径サイジング成形法により成形されたパイプの
場合、押出機ダイスから樹脂がいったん溶融状態で押し
出された後、外部冷却サイジング装置に導かれることか
ら、溶融状態での形状保持性、すなわちドローダウン性
に優れたものであることが必要とされ、比較的分子量分
布の広いエチレン単独重合体もしくは、エチレン・α−
オレフィン共重合体等が使用されてきた。2. Description of the Related Art Conventionally, in the method of molding a polyethylene pipe, the outer diameter is more important than the inner diameter in the pipe dimension control in the construction of the joint connection. Therefore, the outer diameter sizing molding method is used. In general, from the viewpoint of extrusion moldability, general-purpose high-density polyethylene for extrusion molding and low-density polyethylene having a relatively wide molecular weight distribution are used. Since polyethylene pipes have excellent long-term performance and chemical resistance, are inexpensive, and are easy to process, they have been used mainly for water supply and drainage pipes for a long time due to their characteristics. In particular, low-density ethylene / α-olefin copolymer (linear low-density polyethylene) has excellent characteristics such as flexibility and chlorine water resistance.
In recent years, 62 type 1 pipes (soft pipes) have been used.
Further, in the case of a pipe molded by the outer diameter sizing molding method, the resin is extruded from the extruder die in the molten state and then guided to the external cooling sizing device, so that the shape retention in the molten state, that is, the draw It is required to have excellent down property, and an ethylene homopolymer having a relatively wide molecular weight distribution or ethylene / α-
Olefin copolymers and the like have been used.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、前述の
ような比較的分子量分布が広く押出加工性の良い直鎖状
エチレン系重合体を用いて厚肉のパイプを外径サイジン
グ成形法により成形しようとすると、パイプ内面(内
壁)にランダムな筋状の皺が発生し、外観上の商品価値
を損なうと同時に管内流量抵抗の増加等が生じて実用上
大きな問題となることが判明した。このような皺の発生
の詳細なメカニズムは不明であるが、溶融樹脂の流動状
態が不安定(一種の脈動)になること、サイジングダイ
スで溶融樹脂の外径よりも絞られていること、パイプ製
品の肉厚が厚くなると外表面から先に冷却されるため、
その結果として内表面が外表面側へ収縮されること等が
原因ではないかと考えられる。一方、比較的分子量分布
の狭い樹脂を用いて成形すれば皺は発生しないが、樹脂
の溶融張力不足によってドローダウン性が低下し、その
結果として溶融樹脂が垂れて成形が困難になるばかりで
なく、特に低温、高速押出成形の条件下ではパイプの内
外面に肌荒れ現象(通称シャークスキン)が発生し、こ
れも大きな問題となることが知られている。However, it is attempted to form a thick pipe by the outer diameter sizing molding method using the linear ethylene polymer having a relatively wide molecular weight distribution and good extrudability as described above. Then, it was found that random streaky wrinkles are generated on the inner surface (inner wall) of the pipe, which impairs the commercial value in appearance and at the same time increases the flow resistance in the pipe, which is a serious problem in practical use. Although the detailed mechanism of the occurrence of such wrinkles is unclear, the flow state of the molten resin becomes unstable (a kind of pulsation), the sizing die narrows the outer diameter of the molten resin, and the pipe As the product becomes thicker, it cools from the outer surface first,
As a result, it is considered that the cause is that the inner surface is contracted toward the outer surface. On the other hand, wrinkling does not occur if molding is performed using a resin with a relatively narrow molecular weight distribution, but drawdown is deteriorated due to insufficient melt tension of the resin, and as a result, the molten resin sags and molding becomes difficult. It is known that a skin roughening phenomenon (commonly referred to as sharkskin) occurs on the inner and outer surfaces of a pipe particularly under conditions of low temperature and high speed extrusion molding, and this is also a serious problem.
【0004】[0004]
[発明の概要]本発明者らは、前述の問題点を解決する
ために、外径サイジング成形法による厚肉パイプ内面の
皺の発生を防止すべく鋭意研究を重ねた結果、特定のエ
チレン系樹脂に特定の添加剤を配合した組成物を用いる
ことにより、ドローダウン性に優れ、かつ皺の発生しな
いパイプが形成されることを見い出して本発明を完成し
た。すなわち、本発明のエチレン共重合体組成物は、酸
化クロム系フィリップス型触媒によって得られる、MF
Rが0.05〜2g/10分、かつ190℃における溶
融張力が3g以上である直鎖状エチレン・α−オレフィ
ン共重合体にフォスファイト及び/又はフォスフォナイ
トを0.02〜1重量%配合してなることを特徴とする
ものである。[Summary of the Invention] In order to solve the above-mentioned problems, the present inventors have earnestly studied to prevent wrinkles on the inner surface of a thick-walled pipe by an outer diameter sizing molding method, and as a result, a specific ethylene-based The present invention has been completed by finding that a pipe in which a drawdown property is excellent and wrinkle does not occur is formed by using a composition in which a resin is mixed with a specific additive. That is, the ethylene copolymer composition of the present invention is obtained by using a chromium oxide-based Phillips type catalyst, MF
0.02 to 1% by weight of phosphite and / or phosphonite in a linear ethylene / α-olefin copolymer having an R of 0.05 to 2 g / 10 minutes and a melt tension at 190 ° C. of 3 g or more. It is characterized by being mixed.
【0005】[発明の具体的説明] [I] 構成成分 (1) エチレン共重合体 本発明のエチレン共重合体組成物で用いるエチレン共重
合体は、酸化クロム系フィリップス型のイオン重合触媒
を用いて製造した直鎖状重合体であり、気相法、溶液
法、スラリー法、高圧法等いずれの製造法によるもので
も適用でき、主成分のエチレンとエチレン以外のコモノ
マーの一種又は、二種以上を共重合させて得られた共重
合体である。DETAILED DESCRIPTION OF THE INVENTION [I] Constituent Component (1) Ethylene Copolymer The ethylene copolymer used in the ethylene copolymer composition of the present invention uses a chromium oxide-based Phillips type ionic polymerization catalyst. It is a linear polymer produced by, and can be applied by any production method such as a gas phase method, a solution method, a slurry method, a high pressure method, etc., and one or more of ethylene as a main component and a comonomer other than ethylene. It is a copolymer obtained by copolymerizing.
【0006】酸化クロム系フィリップス型触媒以外の、
例えば、チタン及び有機アルミニウムを主成分とするチ
ーグラー型触媒を用いて製造した直鎖状エチレン共重合
体は、該フィリップス型触媒を用いて製造したものに比
較して分子量分布が狭い。このため、分子量分布を広く
するためには高分子量成分と低分子量成分とを別々の条
件で製造する方法、すなわち、バッチ重合法又は2槽以
上の重合槽による連続多槽重合法が採られ得るが、いず
れも該フィリップス型触媒を用いて1槽の重合槽で連続
的に製造する方法に比べて設備も複雑で生産性も劣り好
ましくない。Other than chromium oxide type Phillips type catalyst,
For example, a linear ethylene copolymer produced using a Ziegler type catalyst containing titanium and organoaluminum as a main component has a narrower molecular weight distribution than that produced using the Phillips type catalyst. Therefore, in order to broaden the molecular weight distribution, a method of producing a high molecular weight component and a low molecular weight component under different conditions, that is, a batch polymerization method or a continuous multi-tank polymerization method with two or more tanks can be adopted. However, in both cases, the equipment is complicated and the productivity is inferior as compared with the method of continuously producing in one polymerization tank using the Phillips type catalyst, which is not preferable.
【0007】本発明で用いるエチレン共重合体は、分子
量の目安となるMFR(JIS−K6760、荷重2.
16kg)が0.05〜2g/10分のものが適用で
き、特に0.1〜1g/10分のものが好ましい。これ
らの中でもMFRの低い方の重合体はドローダウン性、
強度等に優れるが、過度に低くて、例えばMFRが0.
05未満のものは成形時の流動性等の成形性が悪くな
る。またMFRが2超過のものはドローダウン性、強度
等が劣る。また、このエチレン共重合体の溶融張力は、
これをJIS−K6760のMFR測定法にて使用する
炉及びノズルから190℃の温度でシリンダー押出棒を
10mm/分の速度で押出し、4m/分の速度で引っ張
ったときの溶融張力が3g以上のものが適用でき、特に
ドローダウン性の観点より4g以上のものが好ましい。The ethylene copolymer used in the present invention has an MFR (JIS-K6760, load 2.
16 kg) of 0.05 to 2 g / 10 minutes can be applied, and 0.1 to 1 g / 10 minutes is particularly preferable. Among these, the polymer with the lower MFR has a drawdown property,
It is excellent in strength, etc., but is too low, for example, MFR is 0.
If it is less than 05, the moldability such as fluidity at the time of molding becomes poor. If the MFR exceeds 2, drawdown property and strength are poor. The melt tension of this ethylene copolymer is
A cylinder extrusion rod is extruded at a speed of 10 mm / min from a furnace and a nozzle used in the MFR measurement method of JIS-K6760 at a temperature of 190 ° C., and a melt tension when pulled at a speed of 4 m / min is 3 g or more. Those having a weight of 4 g or more are preferable, and those having a weight of 4 g or more are particularly preferable from the viewpoint of drawdown property.
【0008】このようなエチレン共重合体は、酸化クロ
ムをシリカ・アルミナ等無機担体等に担持させたもの、
すなわち酸化クロム系フィリップス型触媒を用いて気相
法、溶液法、スラリー法、あるいは圧力500kg/c
m2 以上および温度100〜350℃の条件下での高圧
イオン重合法等の製造プロセスを適用して、主成分のエ
チレンとα‐オレフィンを共重合することで得られる。
エチレンと共重合させる場合のα−オレフィンとして
は、炭素数3〜12程度のα−オレフィン、例えばプロ
ピレン、ブテン−1、ペンテン−1、ヘキセン−1、4
−メチルペンテン−1、オクテン−1等が挙げられる。
特に好ましいα−オレフィンは、炭素数4〜8のもの、
特にブテン−1、ヘキセン−1、4−メチルペンテン−
1及びオクテン−1、である。これらα−オレフィンは
二種以上併用することができる。共重合体中のα−オレ
フィン含量は、0.5〜20重量%、好ましくは1〜1
5重量%である。Such an ethylene copolymer has chromium oxide supported on an inorganic carrier such as silica or alumina,
That is, using a chromium oxide type Phillips catalyst, a gas phase method, a solution method, a slurry method, or a pressure of 500 kg / c.
It can be obtained by applying a production process such as a high-pressure ionic polymerization method under the conditions of m 2 or more and a temperature of 100 to 350 ° C. to copolymerize ethylene as a main component with α-olefin.
When the α-olefin is copolymerized with ethylene, the α-olefin having about 3 to 12 carbon atoms, for example, propylene, butene-1, pentene-1, hexene-1, 4,
-Methylpentene-1, octene-1 and the like.
Particularly preferred α-olefins have 4 to 8 carbon atoms,
Especially butene-1, hexene-1,4-methylpentene-
1 and octene-1. Two or more kinds of these α-olefins can be used in combination. The content of α-olefin in the copolymer is 0.5 to 20% by weight, preferably 1 to 1
It is 5% by weight.
【0009】中でも、エチレン共重合体の密度(JIS
−K6760の試験法による)が0.915〜0.93
0g/cm3 、特に0.920〜0.925g/cm3
のものが耐圧強度、長尺間巻の点で好ましい。これら共
重合体の密度は共重合させたα−オレフィンの種類およ
び(または)含量によって変化する。この共重合体は、
また分子量分布の目安となるFR(荷重10kg時のM
FRと荷重2.16kg時のMFRとの比)が13〜2
5のもの、特に14〜20のもの、が好ましい。FRの
低い方の重合体は衝撃強度等に優れるが、成形時の流動
性等の成形性が低下する傾向がある。また、FRが高い
ほど衝撃強度等が劣る傾向にある。このようなエチレン
重合体は市販のものの中から適宜選んで用いることがで
きる。Above all, the density of the ethylene copolymer (JIS
-According to the test method of K6760) is 0.915 to 0.93
0 g / cm 3 , especially 0.920 to 0.925 g / cm 3
Those having a pressure resistance and long winding are preferable. The density of these copolymers varies depending on the type and / or content of the copolymerized α-olefin. This copolymer is
FR, which is a guide for the molecular weight distribution (M at a load of 10 kg,
The ratio of FR and MFR at a load of 2.16 kg) is 13 to 2
5 and particularly 14 to 20 are preferable. A polymer having a lower FR has excellent impact strength and the like, but the moldability such as fluidity during molding tends to be lowered. Further, the higher the FR, the lower the impact strength and the like. Such an ethylene polymer can be appropriately selected and used from commercially available products.
【0010】(b) フォスファイトおよびフォスフォナイ
ト 本発明のエチレン共重合体組成物において前記エチレン
共重合体に配合されて樹脂組成物を形成する配合剤とし
てはフォスファイトまたはフォスフォナイトである。こ
れらは併用して用いることもできる。上記フォスファイ
トとしては、具体的にトリス(2,4−ジ−t−ブチル
フェニル)フォスファイト、ビス(2,6−ジ−t−ブ
チル−4−メチルフェニル)ペンタエリスリトール−ジ
−フォスファイト、ビス(2,4−ジ−t−ブチルフェ
ニル)ペンタエリスリトール−ジ−フォスファイト、ジ
−ステアリル−ペンタエリスリトール−ジ−フォスファ
イト等を挙げることができるが、水道管として使用する
場合は、加水分解によりパイプの耐塩素水性を悪化さる
ので加水分解し難いトリス(2,4−ジ−t−ブチルフ
ェニル)フォスファイトを使用することが特に好まし
い。また、上記フォスフォナイトとしては、例えばテト
ラキス(2,4−ジ−t−ブチルフェニル)−4,4′
−ビフェニレン−ジ−フォスフォナイトを挙げることが
できる。これらのフォスファイト及び/又はフォスフォ
ナイトの配合量は、エチレン共重合体に対して0.02
〜1重量%である。好ましくは0.03〜0.5重量%
である。この配合量未満では皺発生防止効果が小さく、
一方、この配合量より多くなっても効果は飽和してくる
と同時に製品のコスト高になり、また水道管として使用
する場合、ブリードによる水道水への流出、耐塩素水性
等の問題を生じる傾向になって好ましくない。(B) Phosphite and Phosphonite In the ethylene copolymer composition of the present invention, the compounding agent which is mixed with the ethylene copolymer to form a resin composition is phosphite or phosphonite. These can be used in combination. Specific examples of the phosphite include tris (2,4-di-t-butylphenyl) phosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol-di-phosphite, Bis (2,4-di-t-butylphenyl) pentaerythritol-di-phosphite, di-stearyl-pentaerythritol-di-phosphite and the like can be mentioned, but when used as a water pipe, hydrolysis Therefore, it is particularly preferable to use tris (2,4-di-t-butylphenyl) phosphite, which is difficult to hydrolyze, since it deteriorates the chlorine resistance of the pipe. Examples of the phosphonite include tetrakis (2,4-di-t-butylphenyl) -4,4 '.
-Biphenylene-di-phosphonite can be mentioned. The blending amount of these phosphite and / or phosphonite is 0.02 with respect to the ethylene copolymer.
~ 1% by weight. Preferably 0.03 to 0.5% by weight
Is. If it is less than this amount, the effect of preventing wrinkles is small,
On the other hand, if the amount is larger than this amount, the effect will be saturated and the cost of the product will increase, and when used as a water pipe, problems such as outflow to tap water due to bleed and chlorine resistance will occur. Is not preferable.
【0011】(2) 組成物の調製 上記構成成分を配合して組成物を製造する方法として
は、直接ロール、バンバリー、ニーダー、押出機等の混
練機で溶融混練する方法、配合剤の分散を良くするため
ヘンシェル型ミキサー等で予めエチレン共重合体の粉体
と混合させた後、前述の混練機で溶融混練する方法、あ
るいは一旦高濃度のマスターバッチを作った後に未配合
のエチレン共重合体で希釈する方法等の種々の公知の方
法を適用することができる。また、必要に応じて本発明
の効果を著しく損なわない範囲でポリプロピレン、分岐
状ポリエチレン(高圧法ラジカル重合ポリエチレン)、
エチレン・酢酸ビニル共重合体等の混和可能な他の樹
脂、あるいは他の酸化防止剤、中和剤、滑剤、アンチブ
ロッキング剤、帯電防止剤、紫外線吸収剤、光安定剤、
蛍光増白剤等の添加剤、あるいは有機系顔料、無機系顔
料等の着色剤や充填剤等、を直接または樹脂等のマスタ
ーバッチの形で添加することもできる。但し、これらを
添加することによって皺発生防止効果が低下する場合も
あるので、種類および添加量は注意しなければならな
い。(2) Preparation of composition As a method for preparing a composition by blending the above-mentioned constituents, a method of melt kneading with a kneader such as a direct roll, a Banbury machine, a kneader, an extruder, or a dispersion of a compounding agent is carried out. In order to improve the method, it is mixed with the ethylene copolymer powder in advance with a Henschel type mixer or the like, and then melt-kneaded with the above-mentioned kneader, or an unblended ethylene copolymer after once producing a high-concentration masterbatch. Various known methods such as a method of diluting with can be applied. Further, if necessary, polypropylene, branched polyethylene (high-pressure radical polymerized polyethylene), within a range that does not significantly impair the effects of the present invention,
Other miscible resins such as ethylene / vinyl acetate copolymer, or other antioxidants, neutralizing agents, lubricants, antiblocking agents, antistatic agents, ultraviolet absorbers, light stabilizers,
Additives such as optical brighteners, or colorants such as organic pigments and inorganic pigments and fillers may be added directly or in the form of a masterbatch of resin or the like. However, addition of these may reduce the wrinkle prevention effect, so care must be taken regarding the type and amount of addition.
【0012】上記の本発明の組成物を用いてパイプを成
形する方法は、汎用性があり、かつ外径寸法制御に特徴
を有する外径サイジング成形法が好適であり、成形装置
の大小、構造等に制限しない。但し、本発明の主目的は
肉厚が厚くてもパイプ内面の平滑性を損なわない点にあ
り、これを達成するように改良された樹脂組成物を用い
るため、パイプ肉厚は3mm以上、好ましくは4mm以
上、特に好ましくは6mm以上であるものが大きな効果
を奏する。また、このパイプは必ずしも円形でなくても
よく、例えば長方形等異形押出成形に分類されるものも
含む。なお、この場合の肉厚とは最小肉厚箇所を意味す
る。さらに、本発明の効果が奏される限り多層のパイプ
に成形することもできる。As a method for molding a pipe using the above-mentioned composition of the present invention, an outer diameter sizing molding method which is versatile and characterized in outer diameter dimension control is suitable. It is not limited to etc. However, the main object of the present invention is that even if the wall thickness is large, the smoothness of the inner surface of the pipe is not impaired. Since a resin composition improved to achieve this is used, the wall thickness of the pipe is preferably 3 mm or more, Is 4 mm or more, and particularly preferably 6 mm or more has a great effect. Further, this pipe does not necessarily have to be circular, and includes pipes classified into irregular-shaped extrusion molding such as rectangular. The wall thickness in this case means the minimum wall thickness portion. Further, as long as the effects of the present invention are exhibited, it is possible to form a multilayer pipe.
【0013】[0013]
【実施例】実施例1〜7および比較例1 (イ)樹脂組成物の調製 気相法プロセスにて、微量酸素の存在下、二酸化珪素に
酸化クロムと酸化チタンを担持した通称フィリップス型
イオン重合触媒を用いてエチレンとブテン−1を共重合
させて、MFR0.5g/10分、密度0.922g/
cm3 、FR16の直鎖状エチレン・ブテン−1共重合
体を得た。該共重合体に市販のフォスファイト、フォス
フォナイト、ステアリン酸亜鉛を表1に示す配合量で配
合した後、ヘンシェル型ミキサーで混合し、スクリュー
直径40mmの単軸押出機で溶融混練して樹脂組成物の
ペレットを得た。EXAMPLES Examples 1 to 7 and Comparative Example 1 (a) Preparation of resin composition In the vapor phase process, commonly known as Phillips type ionic polymerization in which chromium oxide and titanium oxide are supported on silicon dioxide in the presence of a trace amount of oxygen. Copolymerization of ethylene and butene-1 using a catalyst, MFR 0.5g / 10min, density 0.922g /
A linear ethylene / butene-1 copolymer having a cm 3 of FR16 was obtained. Commercially available phosphite, phosphonite, and zinc stearate were added to the copolymer in the amounts shown in Table 1, then mixed in a Henschel mixer, and melt-kneaded in a single-screw extruder with a screw diameter of 40 mm to prepare a resin. A pellet of the composition was obtained.
【0014】(ロ)パイプ成形 前記(イ)で得た樹脂組成物ペレットを外径30mm、
内径20mmのストレートダイスを有するスクリュー径
40mmの単軸押出機にて190℃の樹脂温度にて、外
径27mm、内径15mm、肉厚が6mmの寸法になる
ように押出し形成して、真空サイジング装置で外径を制
御しながら水槽でパイプ外面を冷却し単層パイプを得
た。このような成形で得られたパイプ内面の皺発生度合
を目視にて観察して判定した。これらの結果を表1に示
す。なお、表1において添加剤の略記号の意味は次の通
りである。 ・IR168:チバガイギー社製トリス(2,4−ジ−
t−ブチルフェニル)フォスファイト ・PEP36:アデカアーガス社製ビス(2,6−ジ−
t−ブチル−4−メチルフェニル)ペンタエリスリトー
ル−ジ−フォスファイト ・P−EPQ:サンド社製テトラキス(2,4−ジ−t
−ブチルフェニル)−4,4′−ビフェニレン−ジ−フ
ォスフォナイト ・UX624:ボルグワーナー社製ビス(2,4−ジ−
t−ブチルフェニル)ペンタエリスリトール−ジ−フォ
スファイト ・W618:ボルグワーナー社製ジ−ステアリル−ペン
タエリスリトール−ジ−フォスファイト(B) Pipe molding The resin composition pellet obtained in the above (a) was used to obtain an outer diameter of 30 mm,
Vacuum sizing machine using a single screw extruder with a screw diameter of 40 mm and a straight die with an inner diameter of 20 mm to extrude at a resin temperature of 190 ° C. to an outer diameter of 27 mm, an inner diameter of 15 mm and a wall thickness of 6 mm. The outer surface of the pipe was cooled in a water tank while controlling the outer diameter with a single-layer pipe. The degree of wrinkling on the inner surface of the pipe obtained by such molding was visually observed and judged. The results are shown in Table 1. The abbreviations of additives in Table 1 have the following meanings. IR168: Ciba-Geigy tris (2,4-di-
t-Butylphenyl) phosphite PEP36: bis (2,6-di-, manufactured by ADEKA ARGUS CORPORATION
t-Butyl-4-methylphenyl) pentaerythritol-di-phosphite P-EPQ: Tetrakis (2,4-di-t) manufactured by Sand Co.
-Butylphenyl) -4,4'-biphenylene-di-phosphonite UX624: BorgWarner bis (2,4-di-)
t-butylphenyl) pentaerythritol-di-phosphite W618: BorgWarner di-stearyl-pentaerythritol-di-phosphite
【0015】実施例8〜13 エチレン系重合体を表2に示すものに代えた以外は、実
施例4と同様にして評価した。その結果を表2に示す。Examples 8 to 13 Evaluations were made in the same manner as in Example 4 except that the ethylene polymer shown in Table 2 was used. The results are shown in Table 2.
【0016】比較例2〜5 エチレン系重合体を表3に示すものに代え、表3に示す
フォスファイトを用いて実施例1と同様にして評価し
た。その結果を表3に示す。Comparative Examples 2 to 5 The ethylene polymers were replaced with those shown in Table 3 and the phosphites shown in Table 3 were used. The results are shown in Table 3.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【表2】 [Table 2]
【0019】[0019]
【表3】 [Table 3]
【0020】[0020]
【発明の効果】本発明のエチレン共重合体樹脂組成物に
よれば、特定のエチレン共重合体に特定の添加剤を配合
すると、前記した従来技術でのパイプの内面に皺が発生
するといった問題が解決される。更に、従来二次酸化防
止剤として用いられていた特定の燐系化合物を用いるこ
とによってドローダウン性に優れ、パイプ内面の皺発生
の問題が解決されるということは、全く思いがけなかっ
たことである。従って、本発明のエチレン共重合体樹脂
組成物は、厚肉サイズのパイプが必要とされる分野への
実用性の高い成形材料として活用することができる。EFFECTS OF THE INVENTION According to the ethylene copolymer resin composition of the present invention, when a specific additive is added to a specific ethylene copolymer, wrinkles are formed on the inner surface of the pipe in the above-mentioned prior art. Is solved. Furthermore, it was totally unexpected that the use of a specific phosphorus compound that has been conventionally used as a secondary antioxidant has excellent drawdown properties and solves the problem of wrinkling on the inner surface of the pipe. . Therefore, the ethylene copolymer resin composition of the present invention can be utilized as a highly practical molding material in the field where thick-walled pipes are required.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B29L 23:22 4F (72)発明者 須 藤 清 麿 三重県四日市市東邦町1番地 三菱油化株 式会社四日市総合研究所内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Reference number within the agency FI Technical indication location B29L 23:22 4F (72) Inventor Kiyo Maru Suto 1 Toho-cho, Yokkaichi-shi, Mie Mitsubishi Petrochemical Incorporated company Yokkaichi Research Institute
Claims (4)
得られる、MFRが0.05〜2g/10分、かつ19
0℃における溶融張力が3g以上である直鎖状エチレン
・α−オレフィン共重合体にフォスファイト及び/又は
フォスフォナイトを0.02〜1重量%配合してなるこ
とを特徴とする、エチレン共重合体組成物。1. A MFR obtained by a chromium oxide type Phillips type catalyst is 0.05 to 2 g / 10 minutes, and 19
Ethylene copolymer, characterized by comprising 0.02 to 1% by weight of phosphite and / or phosphonite in a linear ethylene / α-olefin copolymer having a melt tension of 3 g or more at 0 ° C. Polymer composition.
が、密度0.915〜0.930g/cm3 の共重合体
である、請求項1に記載のエチレン共重合体組成物。2. The ethylene copolymer composition according to claim 1, wherein the linear ethylene / α-olefin copolymer is a copolymer having a density of 0.915 to 0.930 g / cm 3 .
が、FR(荷重10kg時のMFRと荷重2.16kg
時のMFRとの比)13〜25の共重合体である、請求
項1又は2に記載のエチレン共重合体組成物。3. A linear ethylene / α-olefin copolymer has a FR (MFR at a load of 10 kg and a load of 2.16 kg).
Ethylene copolymer composition according to claim 1 or 2, which is a copolymer having a ratio of MFR to MFR of 13 to 25.
トが、トリス(2,4−ジ−t−ブチルフェニル)フォ
スファイト、ビス(2,6−ジ−t−ブチル−4−メチ
ルフェニル)ペンタエリスリトール−ジ−フォスファイ
ト、ビス(2,4−ジ−t−ブチルフェニル)ペンタエ
リスリトール−ジ−フォスファイト、ジ−ステアリル−
ペンタエリスリトール−ジ−フォスファイト、テトラキ
ス(2,4−ジ−t−ブチルフェニル)−4,4´−ビ
フェニレン−ジ−フォスフォナイトの群から選ばれた少
なくとも1種の化合物である、請求項1〜3のいずれか
に記載のエチレン共重合体組成物。4. Phosphite and / or phosphonite are tris (2,4-di-t-butylphenyl) phosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol. -Di-phosphite, bis (2,4-di-t-butylphenyl) pentaerythritol-di-phosphite, di-stearyl-
The compound is at least one compound selected from the group consisting of pentaerythritol-di-phosphite and tetrakis (2,4-di-t-butylphenyl) -4,4'-biphenylene-di-phosphonite. The ethylene copolymer composition according to any one of 1 to 3.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1270907A JPH0637075B2 (en) | 1989-10-18 | 1989-10-18 | Molding method for resin pipes |
JP5024330A JPH0739516B2 (en) | 1989-10-18 | 1993-02-12 | Ethylene copolymer composition |
JP10252959A JPH11159666A (en) | 1989-10-18 | 1998-09-07 | Supply/discharge water pipe |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1270907A JPH0637075B2 (en) | 1989-10-18 | 1989-10-18 | Molding method for resin pipes |
JP5024330A JPH0739516B2 (en) | 1989-10-18 | 1993-02-12 | Ethylene copolymer composition |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1270907A Division JPH0637075B2 (en) | 1989-10-18 | 1989-10-18 | Molding method for resin pipes |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10252959A Division JPH11159666A (en) | 1989-10-18 | 1998-09-07 | Supply/discharge water pipe |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0673244A true JPH0673244A (en) | 1994-03-15 |
JPH0739516B2 JPH0739516B2 (en) | 1995-05-01 |
Family
ID=26361824
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1270907A Expired - Lifetime JPH0637075B2 (en) | 1989-10-18 | 1989-10-18 | Molding method for resin pipes |
JP5024330A Expired - Lifetime JPH0739516B2 (en) | 1989-10-18 | 1993-02-12 | Ethylene copolymer composition |
JP10252959A Pending JPH11159666A (en) | 1989-10-18 | 1998-09-07 | Supply/discharge water pipe |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1270907A Expired - Lifetime JPH0637075B2 (en) | 1989-10-18 | 1989-10-18 | Molding method for resin pipes |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10252959A Pending JPH11159666A (en) | 1989-10-18 | 1998-09-07 | Supply/discharge water pipe |
Country Status (1)
Country | Link |
---|---|
JP (3) | JPH0637075B2 (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5013438A (en) * | 1973-06-06 | 1975-02-12 | ||
JPH0216137A (en) * | 1988-05-06 | 1990-01-19 | Union Carbide Corp | Stabilization of crosslinked vldpe |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60163947A (en) * | 1984-02-06 | 1985-08-26 | Mitsubishi Petrochem Co Ltd | Polyethylene composition |
JPS6456747A (en) * | 1987-08-27 | 1989-03-03 | Mitsubishi Petrochemical Co | Pipe for plumbing system |
JPS6487989A (en) * | 1987-09-29 | 1989-04-03 | Mitsubishi Petrochemical Co | Plumbing transfer pipe |
JPS6487990A (en) * | 1987-09-29 | 1989-04-03 | Mitsubishi Petrochemical Co | Plumbing pipe |
JPH01203787A (en) * | 1988-02-05 | 1989-08-16 | Mitsubishi Petrochem Co Ltd | Supplied/discharged water transporting pipe |
US4863983A (en) * | 1988-04-15 | 1989-09-05 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
-
1989
- 1989-10-18 JP JP1270907A patent/JPH0637075B2/en not_active Expired - Lifetime
-
1993
- 1993-02-12 JP JP5024330A patent/JPH0739516B2/en not_active Expired - Lifetime
-
1998
- 1998-09-07 JP JP10252959A patent/JPH11159666A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5013438A (en) * | 1973-06-06 | 1975-02-12 | ||
JPH0216137A (en) * | 1988-05-06 | 1990-01-19 | Union Carbide Corp | Stabilization of crosslinked vldpe |
Also Published As
Publication number | Publication date |
---|---|
JPH11159666A (en) | 1999-06-15 |
JPH0739516B2 (en) | 1995-05-01 |
JPH0637075B2 (en) | 1994-05-18 |
JPH03132327A (en) | 1991-06-05 |
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