JPH05163388A - Polyolefin resin composition excellent in impact resistance - Google Patents
Polyolefin resin composition excellent in impact resistanceInfo
- Publication number
- JPH05163388A JPH05163388A JP29575591A JP29575591A JPH05163388A JP H05163388 A JPH05163388 A JP H05163388A JP 29575591 A JP29575591 A JP 29575591A JP 29575591 A JP29575591 A JP 29575591A JP H05163388 A JPH05163388 A JP H05163388A
- Authority
- JP
- Japan
- Prior art keywords
- block copolymer
- weight
- hydrogenated block
- hydrogenated
- conjugated diene
- 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
- 229920005672 polyolefin resin Polymers 0.000 title claims abstract description 13
- 239000011342 resin composition Substances 0.000 title 1
- 229920001400 block copolymer Polymers 0.000 claims abstract description 54
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 38
- 229920000642 polymer Polymers 0.000 claims abstract description 22
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 21
- 150000001993 dienes Chemical class 0.000 claims abstract description 13
- -1 vinyl aromatic compounds Chemical class 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 31
- 229920000098 polyolefin Polymers 0.000 claims description 14
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract description 8
- 238000000465 moulding Methods 0.000 abstract description 4
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- 238000013329 compounding Methods 0.000 abstract 2
- 229920001577 copolymer Polymers 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 238000005481 NMR spectroscopy Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 description 1
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 description 1
- QEDJMOONZLUIMC-UHFFFAOYSA-N 1-tert-butyl-4-ethenylbenzene Chemical compound CC(C)(C)C1=CC=C(C=C)C=C1 QEDJMOONZLUIMC-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- PKZCRWFNSBIBEW-UHFFFAOYSA-N 2-n,2-n,2-trimethylpropane-1,2-diamine Chemical compound CN(C)C(C)(C)CN PKZCRWFNSBIBEW-UHFFFAOYSA-N 0.000 description 1
- QTTAWIGVQMSWMV-UHFFFAOYSA-N 3,4-dimethylhexa-1,3-diene Chemical compound CCC(C)=C(C)C=C QTTAWIGVQMSWMV-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N 4-methylpenta-1,3-diene Chemical compound CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- FKSJCZAVZLBVHS-UHFFFAOYSA-N [Ti]C1=CC=CC1 Chemical compound [Ti]C1=CC=CC1 FKSJCZAVZLBVHS-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、衝撃強度、特に低温時
における耐衝撃性と剛性のバランス、さらに流動加工性
に優れた、ポリオレフィンと特定構造の水素添加ブロッ
ク共重合体とを含むポリオレフィン組成物に関する。FIELD OF THE INVENTION The present invention relates to a polyolefin composition containing a polyolefin and a hydrogenated block copolymer having a specific structure, which is excellent in impact strength, particularly in balance of impact resistance and rigidity at low temperature, and has excellent flow processability. Regarding things.
【0002】[0002]
【従来の技術】ポリオレフィン系樹脂は、一般に耐薬品
性、機械的特性に優れているため、機械部品、自動車部
品から家庭用品、各種容器など広範に使用されている。
しかしながら、耐衝撃強度、特に低温時における衝撃強
度が不足しており、使用目的が限定されることもある。
そこで、この問題点を改良する目的でゴム成分をポリオ
レフィンに添加する提案が数多くなされている。例え
ば、特公昭42−19935号公報、特公昭46−85
85号公報、特公昭46−16429号公報、特公昭4
7−26369号公報には、ポリオレフィン系樹脂に、
スチレン−ブタジエンブロック共重合体、熱可塑性エラ
ストマーを添加することにより、耐衝撃性や耐ストレス
クラッキング性が改良されることが示されている。2. Description of the Related Art Polyolefin resins are generally used for various purposes such as mechanical parts, automobile parts, household products, and various containers because they are excellent in chemical resistance and mechanical properties.
However, the impact resistance, especially the impact strength at low temperature, is insufficient, and the purpose of use may be limited.
Therefore, many proposals have been made to add a rubber component to polyolefin for the purpose of improving this problem. For example, Japanese Patent Publication No. 42-19935 and Japanese Patent Publication No. 46-85.
Japanese Patent Publication No. 85, Japanese Patent Publication No. 46-16429, Japanese Patent Publication No. 4
No. 7,26,369 discloses a polyolefin resin,
It has been shown that impact resistance and stress cracking resistance are improved by adding a styrene-butadiene block copolymer and a thermoplastic elastomer.
【0003】しかし、これらの方法では通常のブロック
共重合体を用いているため、耐衝撃性の改良が十分でな
く、なお一層の改善が要望されていた。また、ゴム成分
を添加する弊害として剛性の低下、あるいは流動加工性
の低下をもたらすことがある。これらの点を改良する目
的で、ゴム成分に水添ジエン系ランダム共重合体を用い
た特開平2−158643号公報、特定分子量のブロッ
ク共重合体を用いた特開平3−76744号公報が示さ
れている。しかしながら、このようにして改良された組
成物は、実際に必要とされる低温時の耐衝撃性について
は十分なものではなく、さらに一層の改良が要望されて
いた。However, since the conventional block copolymers are used in these methods, the impact resistance is not sufficiently improved, and further improvement has been demanded. Further, as a harmful effect of adding the rubber component, there is a case where rigidity is lowered or flow processability is lowered. For the purpose of improving these points, JP-A-2-158643 using a hydrogenated diene random copolymer as a rubber component and JP-A-3-76744 using a block copolymer having a specific molecular weight are disclosed. Has been done. However, the composition improved in this way is not sufficient in the impact resistance at low temperature actually required, and further improvement has been demanded.
【0004】本発明者等は、上記問題点を改良するもの
として、すでに、特定構造を有する水素添加ブロック共
重合体とポリオレフィン系樹脂からなる組成物を提案し
た(特願平3−111850号明細書)。低温衝撃強
度、流動加工性については著しく改良された発明であっ
た。The present inventors have already proposed a composition comprising a hydrogenated block copolymer having a specific structure and a polyolefin resin as a solution to the above problems (Japanese Patent Application No. 3-111850). book). The invention was remarkably improved in low temperature impact strength and flow processability.
【0005】[0005]
【発明が解決しようとする課題】本発明の目的は、耐衝
撃性、特に実用的な低温時の耐衝撃性と剛性のバランス
に優れ、かつ射出成形や押出成形に適した優れた流動加
工性を有するポリオレフィン組成物を提供することにあ
る。The object of the present invention is to have excellent impact resistance, in particular, a good balance between impact resistance and rigidity at practical low temperatures, and excellent flow processability suitable for injection molding and extrusion molding. Another object of the present invention is to provide a polyolefin composition having
【0006】[0006]
【課題を解決するための手段】本発明者らは、ビニル芳
香族化合物ブロック−共役ジエン化合物ブロック共重合
体の水素添加物のポリマー構造とポリオレフィン組成物
の物性との相関について、さらに鋭意検討を重ねた結
果、低温衝撃強度と剛性、流動加工性に優れた組成物を
得るために、特定構造の水素添加ブロック共重合体をポ
リオレフィン系樹脂に混合することによりその目的が達
成されることを見出し、本発明を完成するに到った。[Means for Solving the Problems] The present inventors have made further studies on the correlation between the polymer structure of the hydrogenated product of the vinyl aromatic compound block-conjugated diene compound block copolymer and the physical properties of the polyolefin composition. As a result of stacking, in order to obtain a composition excellent in low-temperature impact strength, rigidity, and flow processability, it was found that the purpose can be achieved by mixing a hydrogenated block copolymer having a specific structure with a polyolefin resin. The present invention has been completed.
【0007】即ち、本発明は、 (1) ポリオレフィン系樹脂 95〜50重量部 (2)(a)少なくとも2個のビニル芳香族化合物を主
体とする重合体ブロックAと少なくとも1個の共役ジエ
ン化合物を主体とする重合体ブロックBを有し、その共
役ジエン部分の80%以上が水素添加され、水添前のビ
ニル結合量が40〜60%であり、(b)よりも高分子
量の水素添加ブロック共重合体(b)少なくとも2個の
ビニル芳香族化合物を主体とする重合体ブロックCと少
なくとも1個の共役ジエン化合物を主体とする重合体ブ
ロックDを有し、その共役ジエン部分の80%以上が水
素添加され、水添前のビニル結合量が40〜60%であ
り、数平均分子量が4.5万を越える水素添加ブロック
共重合体とからなり、 (a)がブロック共重合体中 10重量%以上40重量
%未満 (b)がブロック共重合体中 60重量%を越え90重
量%以下 (a)と(b)との数平均分子量(MN ) の算術平均
が、50,000〜150,000である水素添加ブロ
ック共重合体 5〜50重量部よりなるポリオレフィン
組成物である。That is, the present invention provides (1) a polyolefin resin 95 to 50 parts by weight (2) (a) a polymer block A mainly containing at least two vinyl aromatic compounds and at least one conjugated diene compound. Having a polymer block B mainly composed of hydrogen peroxide, 80% or more of the conjugated diene portion of which is hydrogenated, the amount of vinyl bond before hydrogenation is 40 to 60%, and the hydrogenation has a higher molecular weight than that of (b). Block copolymer (b) having at least two vinyl aromatic compound-based polymer blocks C and at least one conjugated diene compound-based polymer block D, and 80% of the conjugated diene moieties The above is a hydrogenated block copolymer which is hydrogenated, has a vinyl bond content of 40 to 60% before hydrogenation, and has a number average molecular weight of more than 45,000, wherein (a) is a block copolymer. During the arithmetic mean of the number average molecular weight of 10 wt% or more and less than 40 wt% (b) exceeds 60 wt% in the block copolymer 90 wt% or less (a) and (b) (M N) is 50, It is a polyolefin composition consisting of 5 to 50 parts by weight of a hydrogenated block copolymer of 000 to 150,000.
【0008】本発明の組成物中の(2)の成分である水
素添加ブロック共重合体は、(a)少なくとも2個のビ
ニル芳香族化合物を主体とする重合体ブロックAと少な
くとも1個の共役ジエン化合物を主体とする重合体ブロ
ックBを有し、その共役ジエン部分の80%以上が水素
添加され、水添前のビニル結合量が40〜60%である
高分子量の水素添加ブロック共重合体と(b)少なくと
も2個のビニル芳香族化合物を主体する重合体ブロック
Cと少なくとも1個の共役ジエン化合物を主体とする重
合体ブロックDを有し、その共役ジエン部分の80%以
上が水素添加され、水添前のビニル結合量が40〜60
%である数平均分子量が4.5万を越える水素添加ブロ
ック共重合体からなる。The hydrogenated block copolymer which is the component (2) in the composition of the present invention comprises (a) a polymer block A containing at least two vinyl aromatic compounds as a main component and at least one conjugate. A high molecular weight hydrogenated block copolymer having a polymer block B containing a diene compound as a main component, 80% or more of its conjugated diene portion being hydrogenated, and having a vinyl bond content before hydrogenation of 40 to 60%. And (b) having a polymer block C mainly containing at least two vinyl aromatic compounds and a polymer block D mainly containing at least one conjugated diene compound, and 80% or more of the conjugated diene portion being hydrogenated And the amount of vinyl bond before hydrogenation is 40 to 60
% Hydrogenated block copolymer having a number average molecular weight of more than 45,000.
【0009】(b)よりも高分子量のブロック共重合体
(a)と(a)よりも低分子量のブロック共重合体
(b)とはその構造、ビニル芳香族化合物量や水添前の
ビニル結合量等のミクロ構造は、同一であってもよい
し、異なるものであってもかまわない。ビニル芳香族化
合物を主体とする重合体ブロックA,Cは、ビニル芳香
族化合物と共役ジエン化合物との重量比が100/0〜
51/49、好ましくは100/0〜70/30の組成
範囲からなる重合体ブロックであり、ビニル芳香族化合
物と共役ジエン化合物が共重合した場合、このブロック
における共役ジエン化合物の分布は、ランダム、テーパ
ー(分子鎖に沿ってモノマー成分が増加または減少する
もの)、一部ブロック状又はこれらの任意の組合せのい
ずれであってもよい。The block copolymer (a) having a higher molecular weight than that of (b) and the block copolymer (b) having a lower molecular weight than that of (a) have a structure, vinyl aromatic compound amount and vinyl before hydrogenation. The microstructures such as the amount of binding may be the same or different. The polymer blocks A and C mainly containing a vinyl aromatic compound have a weight ratio of the vinyl aromatic compound and the conjugated diene compound of 100/0 to
51/49, preferably a polymer block having a composition range of 100/0 to 70/30. When a vinyl aromatic compound and a conjugated diene compound are copolymerized, the distribution of the conjugated diene compound in this block is random, It may be tapered (in which the monomer component increases or decreases along the molecular chain), partially block-shaped, or any combination thereof.
【0010】また、共役ジエン化合物を主体とする重合
体ブロックB,Dは、ビニル芳香族化合物と共役ジエン
化合物との重量比が0/100〜49/51、好ましく
は0/100〜30/70の組成範囲からなる重合体ブ
ロックであり、共役ジエン化合物とビニル芳香族化合物
が共重合した場合、このブロックにおけるビニル芳香族
化合物の分布は、ランダム、テーパー(分子鎖に沿って
モノマー成分が増加または減少するもの)、一部ブロッ
ク状又はこれらの任意の組合せのいずれであってもよ
い。In the polymer blocks B and D mainly composed of the conjugated diene compound, the weight ratio of the vinyl aromatic compound and the conjugated diene compound is 0/100 to 49/51, preferably 0/100 to 30/70. When the conjugated diene compound and the vinyl aromatic compound are copolymerized, the distribution of the vinyl aromatic compound in this block is random or tapered (the monomer component increases along the molecular chain or Decrease), partial block, or any combination thereof.
【0011】ここで供するビニル芳香族化合物として
は、スチレン、α−メチルスチレン、p−メチルスチレ
ンやp−ターシャリブチルスチレン等のアルキルスチレ
ン、パラメトキシスチレン、ビニルナフタレン等のうち
から1種又は2種以上が選ばれ、中でもスチレン、p−
メチルスチレンが特に好ましい。また共役ジエン化合物
としては、ブタジエン、イソプレン、ピペリレン、メチ
ルペンタジエン、フェニルブタジエン、3,4−ジメチ
ル−1,3−ヘキサジエン、4,5−ジエチル−1,3
−オクタジエン等のうちから1種又は2種以上が選ば
れ、中でもブタジエン及び/又はイソプレンが特に好ま
しい。The vinyl aromatic compound provided here is one or two of styrene, alkylstyrene such as α-methylstyrene, p-methylstyrene and p-tert-butylstyrene, paramethoxystyrene, vinylnaphthalene and the like. More than one species are selected, among them styrene, p-
Methylstyrene is particularly preferred. Examples of the conjugated diene compound include butadiene, isoprene, piperylene, methylpentadiene, phenylbutadiene, 3,4-dimethyl-1,3-hexadiene, 4,5-diethyl-1,3.
-One or more selected from octadiene and the like, and among them, butadiene and / or isoprene are particularly preferable.
【0012】ビニル芳香族化合物の含有量は、10〜5
0重量%の範囲が好ましく、10〜30重量%の範囲が
更に好ましい。ビニル芳香族化合物の含有量が50重量
%を越える場合は、ポリオレフィン組成物の耐衝撃性の
改良が得られないことがあり、また10重量%未満の場
合は、剛性の低下が著しくなる傾向となる。共役ジエン
部分のミクロ構造は、水添前のビニル結合量が40〜6
0%である必要があり、さらに45〜55%の範囲内に
あるのが、特に好ましい。ここにビニル結合量とは、ブ
ロック共重合体中に1,2−結合、3,4−結合及び
1,4−結合の結合様式で組込まれている共役ジエン化
合物のうち、1,2−結合及び3,4−結合で組込まれ
ているものの割合とする。The content of vinyl aromatic compound is 10 to 5
The range of 0% by weight is preferable, and the range of 10 to 30% by weight is more preferable. When the content of the vinyl aromatic compound exceeds 50% by weight, the impact resistance of the polyolefin composition may not be improved, and when it is less than 10% by weight, the rigidity tends to be remarkably lowered. Become. The microstructure of the conjugated diene portion has a vinyl bond content of 40 to 6 before hydrogenation.
It is necessary to be 0%, and it is particularly preferable to be in the range of 45 to 55%. Here, the vinyl bond content means the 1,2-bond among the conjugated diene compounds incorporated in the block copolymer in the bonding modes of 1,2-bond, 3,4-bond and 1,4-bond. And the proportion of those incorporated with 3,4-bonds.
【0013】ビニル結合量が40%未満であると、ポリ
オレフィン組成物にした際、低温における衝撃強度と流
動加工性の改良が不十分であり、またそれが60%を越
えると、再び、低温における衝撃強度が低下し、また剛
性も低下する。共役ジエン部分のミクロ構造は核磁気共
鳴装置(NMR)により分析する。本発明の水素添加ブ
ロック共重合体は(a),(b)からなる水素添加ブロ
ック共重合体であり、(a)成分が(b)成分よりも高
分子量であり、(b)成分の数平均分子量が4.5万を
越えるものであり、(a)が10重量%以上40重量%
未満、(b)が60重量%を越え90重量%以下である
ことが必要である。そして、(a)と(b)との数平均
分子量の算術平均は50,000〜150,000の範
囲である。また、(a)と(b)との数平均分子量の比
MN (a)/MN (b)は1.1〜4.5が好ましく、
1.2〜2.2が更に好ましい。When the vinyl bond content is less than 40%, the improvement in impact strength and flow processability at low temperature when the composition is made into a polyolefin is insufficient, and when it exceeds 60%, it is again at low temperature. Impact strength decreases and rigidity also decreases. The microstructure of the conjugated diene moiety is analyzed by nuclear magnetic resonance (NMR). The hydrogenated block copolymer of the present invention is a hydrogenated block copolymer comprising (a) and (b), in which the component (a) has a higher molecular weight than the component (b) and the number of components (b) is The average molecular weight exceeds 45,000, and (a) is 10% by weight or more and 40% by weight.
And (b) is more than 60% by weight and 90% by weight or less. The arithmetic average of the number average molecular weights of (a) and (b) is in the range of 50,000 to 150,000. The ratio M N (a) / M N (b) of the number average molecular weights of (a) and (b) is preferably 1.1 to 4.5,
1.2 to 2.2 are more preferable.
【0014】(a)と(b)の個々の数平均分子量は、
ゲルパミュエーションクロマトグラフィー(GPC)で
常法により測定できる。その製法は、例えば、別々に
(b)より高分子量の水素添加ブロック共重合体(a)
と(b)の水素添加ブロック共重合体とを製造し、ブレ
ンドすればよい。ポリオレフィン組成物にした場合、
(b)の割合が、60重量%以下になると、耐衝撃性と
剛性と流動加工性のバランスが悪くなり、90重量%を
越えると、肝要の低温時の面衝撃強度が劣ってしまう。
また、(b)の数平均分子量が4.5万以下であった
り、(a),(b)の数平均分子量の算術平均が50,
000未満であると、耐衝撃性も含め、引張強度等の機
械的強度が低いものとなり、150,000を越える
と、耐衝撃性と剛性が著しく低下し、さらに流動加工性
も劣ったものになってしまう。The individual number average molecular weights of (a) and (b) are
It can be measured by gel permeation chromatography (GPC) by a conventional method. The production method is, for example, that the hydrogenated block copolymer (a) having a higher molecular weight than (b) is separately prepared.
And (b) the hydrogenated block copolymer may be produced and blended. When made into a polyolefin composition,
If the proportion of (b) is less than 60% by weight, the balance between impact resistance, rigidity and flow processability will be poor, and if it exceeds 90% by weight, the surface impact strength at low temperatures, which is essential, will be poor.
Further, the number average molecular weight of (b) is 45,000 or less, or the arithmetic average of the number average molecular weights of (a) and (b) is 50,
If it is less than 000, mechanical strength such as tensile strength will be low, including impact resistance, and if it exceeds 150,000, impact resistance and rigidity will be remarkably lowered, and flowability will be poor. turn into.
【0015】また、上記ブロック共重合体の分子構造
は、直鎖状、分岐状、放射状またはこれらの組合せなど
いずれでもよい。そして、ビニル芳香族化合物を主体と
する重合体ブロックあるいは共役ジエンを主体とするブ
ロックのそれぞれは、同一の構造であってもよいし、モ
ノマー成分含有量、それらの分子鎖における分布、ブロ
ックの分子量、ミクロ構造などの各構造が異なるもので
あってもよい。The molecular structure of the block copolymer may be linear, branched, radial or a combination thereof. And, each of the polymer block mainly composed of vinyl aromatic compound or the block mainly composed of conjugated diene may have the same structure, the monomer component content, the distribution in their molecular chains, the molecular weight of the block. Each structure such as a micro structure may be different.
【0016】ブロック共重合体の製造法としては、例え
ば特公昭36−19286号公報、特公昭43−149
79号公報、特公昭49−36957号公報などに記載
された方法が挙げられる。これらは、炭化水素溶剤中で
アニオン重合開始剤として有機リチウム化合物等を用
い、ビニル化剤としてジエチルエーテル、テトラヒドロ
フランの如きエーテル化合物、トリエチルアミン、N,
N,N′,N′−テトラメチルエチレンジアミンの如き
第3級アミン、必要に応じカップリング剤としてエポキ
シ化ダイズ油、四塩化ケイ素の如き多官能性化合物を用
い、ビニル芳香族化合物と共役ジエン化合物をブロック
共重合する方法であり、直鎖状、分岐状あるいは放射状
の構造を有するブロック共重合体として得られる、本発
明においては、いかなる重合法で得られたものであって
も、上記のものであれば使用可能である。The block copolymer can be produced by, for example, Japanese Patent Publication No. 36-19286 and Japanese Patent Publication No. 43-149.
79, Japanese Patent Publication No. 49-36957 and the like. In these, an organic lithium compound or the like is used as an anionic polymerization initiator in a hydrocarbon solvent, an ether compound such as diethyl ether or tetrahydrofuran as a vinylating agent, triethylamine, N,
Tertiary amines such as N, N ', N'-tetramethylethylenediamine, epoxidized soybean oil as a coupling agent, and polyfunctional compounds such as silicon tetrachloride are used as needed, and vinyl aromatic compounds and conjugated diene compounds are used. A block copolymer having a linear, branched or radial structure, which is obtained by any polymerization method in the present invention. If it can be used.
【0017】上記のブロック共重合体を、公知の方法、
例えば、特公昭42−8704号公報に記載の方法、あ
るいは、特開昭59−133203号公報や特開昭60
−79005号公報に記載の方法で水添することにより
水添ブロック共重合体は得られる。本発明は、共役ジエ
ン部分の80%以上を水素添加させる必要がある。水素
添加の割合が低いと、ポリオレフィン系樹脂との相溶性
が不十分で耐衝撃性が低いものとなり、また、混合、成
形時の熱劣化を受けやすく好ましくない。水素添加率
は、核磁気共鳴装置(NMR)を用いた機器分析により
分析する。The above block copolymer is prepared by a known method,
For example, the method described in JP-B-42-8704, or JP-A-59-133203 and JP-A-60.
A hydrogenated block copolymer can be obtained by hydrogenating according to the method described in JP-A-79005. The present invention requires that 80% or more of the conjugated diene moieties be hydrogenated. When the proportion of hydrogenation is low, the compatibility with the polyolefin resin is insufficient and the impact resistance is low, and it is not preferable because it is susceptible to thermal deterioration during mixing and molding. The hydrogenation rate is analyzed by instrumental analysis using a nuclear magnetic resonance apparatus (NMR).
【0018】本発明で用いる水素添加ブロック共重合体
は、不飽和カルボン酸又はその誘導体との付加反応によ
り変性させ、官能基を含有したものでもかまわない。変
性した水素添加ブロック共重合体は、塗装を必要とする
場合に有利である。本発明の組成物の(1)成分である
ポリオレフィン系樹脂は、α−オレフィン、例えば、エ
チレン、プロピレン、1−ブテン、イソブチレン、4−
メチル−1−ペンテン等を重合して得られる樹脂であれ
ばいずれでもよいが、なかでも、ポリエチレン、ポリプ
ロピレン、ポリブテン、ポリメチルペンテン、エチレン
−プロピレンブロック共重合体またはこれらの混合物が
挙げられる。特に好ましいのは、ポリプロピレンであ
る。The hydrogenated block copolymer used in the present invention may be modified by an addition reaction with an unsaturated carboxylic acid or a derivative thereof to contain a functional group. Modified hydrogenated block copolymers are advantageous when painting is required. The polyolefin resin which is the component (1) of the composition of the present invention is an α-olefin, for example, ethylene, propylene, 1-butene, isobutylene, 4-.
Any resin can be used as long as it is a resin obtained by polymerizing methyl-1-pentene and the like. Among them, polyethylene, polypropylene, polybutene, polymethylpentene, ethylene-propylene block copolymer or a mixture thereof can be mentioned. Especially preferred is polypropylene.
【0019】本発明のポリオレフィン組成物において、
その組成は、(1)成分のポリオレフィン系樹脂が95
〜50重量部、(2)成分の水素添加ブロック共重合体
が5〜50重量部、好ましくは10〜30重量部であ
る。水素添加ブロック共重合体の割合が5重量部未満の
場合には、耐衝撃性、特に低温時における耐衝撃性の改
善効果がそれほど顕著でなく、また、50重量部を越え
ると、剛性等が低い成形材料となってしまい、実用的で
なくなる。In the polyolefin composition of the present invention,
The composition of the (1) component polyolefin resin is 95
To 50 parts by weight, and the hydrogenated block copolymer of the component (2) is 5 to 50 parts by weight, preferably 10 to 30 parts by weight. If the proportion of the hydrogenated block copolymer is less than 5 parts by weight, the effect of improving impact resistance, especially at low temperature, is not so remarkable, and if it exceeds 50 parts by weight, the rigidity and the like are not improved. It becomes a low molding material and becomes impractical.
【0020】本発明の組成物は、その各成分の組成比に
応じて通常の高分子物質の混合に供される装置によって
調製できる。それら混合装置としては、例えば、押出
機、ミキシングロール、ニーダー等があげられ、特に、
本発明では押出機による溶融混合法が好ましい。また、
本発明のポリオレフィン組成物には、その性質を損なわ
ない程度に、炭酸カルシウム、タルク、シリカ、カーボ
ンブラック、ガラス繊維、クレーなどの補強剤ないしは
充填剤を添加することも可能である。また、その他の添
加剤、例えば、熱安定剤、酸化防止剤、紫外線吸収剤、
着色剤、顔料などを添加してもよく、更に本発明の組成
物に発泡剤を加えて発泡体とすることも可能である。The composition of the present invention can be prepared by an apparatus which is usually used for mixing polymer substances depending on the composition ratio of each component. Examples of the mixing device include an extruder, a mixing roll, a kneader, and the like.
In the present invention, the melt mixing method using an extruder is preferable. Also,
To the polyolefin composition of the present invention, it is possible to add a reinforcing agent or a filler such as calcium carbonate, talc, silica, carbon black, glass fiber or clay to the extent that the properties are not impaired. Also, other additives, for example, heat stabilizers, antioxidants, ultraviolet absorbers,
Colorants, pigments and the like may be added, and a foaming agent may be added to the composition of the present invention to form a foam.
【0021】本発明のポリオレフィン組成物は、従来か
らの各種の成形法、例えば射出成形、押出成形等により
成形が可能であり、成形品、シート等、各種分野におい
て広い利用範囲があり、有用である。The polyolefin composition of the present invention can be molded by various conventional molding methods such as injection molding and extrusion molding, and has a wide range of applications in various fields such as molded articles and sheets, and is useful. is there.
【0022】[0022]
【実施例】本発明をより具体的かつ詳細に説明するため
に、次に実施例を示すが、本発明はこれらの例によって
何ら限定されるものではない。尚、実施例及び比較例に
示した物性の測定規格、試験法は以下の通りである。 耐衝撃性(低温) 組成物を射出成形により厚さ2mm、20cm×20c
mのシートを成形し、−30℃の状態でホルダーに固定
し、これに重さ13.7Kgのミサイル型の重りを1.
5mの高さより落下(5.4m/sec)させ、シート
が脆性破壊するか延性破壊するかを確認した。EXAMPLES In order to describe the present invention more specifically and in detail, the following examples are shown, but the present invention is not limited to these examples. The measurement standards and test methods for physical properties shown in Examples and Comparative Examples are as follows. Impact resistance (low temperature) 2mm thick, 20cm x 20c by injection molding the composition
m sheet was molded and fixed to a holder at −30 ° C., and a 13.7 kg missile type weight was added to the holder.
It was dropped from a height of 5 m (5.4 m / sec), and it was confirmed whether the sheet was brittle or ductile.
【0023】 曲げ弾性率 JIS K7203に従って測定。 流動性(MFR) JIS K7210に従って測定。(230℃,2.1
6Kg荷重) (I) 水素添加ブロック共重合体の調整 n−ブチルリチウムを重合触媒とし、シクロヘキサ
ン溶媒中で、テトラヒドロフランをビニル含量調節剤と
して、スチレンとブタジエンをアニオンブロック共重合
することにより、表1に示したようなブロック共重合体
を合成した。尚、ポリマー構造は、モノマーの仕込、分
子量は、触媒量、ビニル含量はビニル含量調節剤を変化
させることによりコントロールした。[0023] Flexural modulus Measured according to JIS K7203. Flowability (MFR) Measured according to JIS K7210. (230 ° C, 2.1
(6 kg load) (I) Preparation of hydrogenated block copolymer By using n-butyllithium as a polymerization catalyst and tetrahydrofuran as a vinyl content modifier in a cyclohexane solvent, anion block copolymerization of styrene and butadiene was performed. A block copolymer as shown in 1 was synthesized. The polymer structure was controlled by changing the charge of the monomers, the molecular weight by changing the catalyst amount, and the vinyl content by changing the vinyl content modifier.
【0024】スチレン含有量は、紫外分光高度計(U
V)を、ビニル含量は、核磁気共鳴装置(NMR)を、
数平均分子量は、ゲルパミュエーションクロマトグラフ
ィーを用いて測定した。The styrene content is measured by an ultraviolet spectrophotometer (U
V), vinyl content, nuclear magnetic resonance (NMR),
The number average molecular weight was measured using gel permeation chromatography.
【0025】[0025]
【表1】 [Table 1]
【0026】 次に各ブロック共重合体をジ−p−ト
リスビス(1−シクロペンタジエニル)チタニウムとn
−ブチルリチウムを水添触媒として、水素圧5Kg/c
m2 、温度50℃で2時間水素添加を行なった。各サン
プルの水素添加率(水添率)を表1の右欄に示した。ブ
タジエンブロック部分の二重結合の90%以上は水素添
加され、スチレンブロック部分のベンゼン環はほとんど
水添されないで残った。尚、b−7は、b−1と同じポ
リマーで、水素添加反応を行なわなかったものである。Next, each block copolymer was treated with di-p-trisbis (1-cyclopentadienyl) titanium and n.
-Butyllithium as hydrogenation catalyst, hydrogen pressure 5 Kg / c
Hydrogenation was carried out at m 2 and temperature of 50 ° C. for 2 hours. The hydrogenation rate (hydrogenation rate) of each sample is shown in the right column of Table 1. 90% or more of the double bonds in the butadiene block portion were hydrogenated, and the benzene ring in the styrene block portion remained almost unhydrogenated. In addition, b-7 is the same polymer as b-1, which is not subjected to hydrogenation reaction.
【0027】水素添加率は核磁気共鳴装置(NMR)を
用いて判定した。 (II) ポリプロピレン組成物の調整と物性測定 市販ポリプロピレン(旭化成(社)製 M8619<M
FR=14(g/10分)>)に、得られた水素添加ブ
ロック共重合体を表2、表3に示した割合で加え、30
mmの2軸押出機により220℃の温度で溶融混練を行
ない、ペレット化した。The hydrogenation rate was determined by using a nuclear magnetic resonance apparatus (NMR). (II) Preparation of polypropylene composition and measurement of physical properties Commercially available polypropylene (M8619 <M manufactured by Asahi Kasei Corporation)
FR = 14 (g / 10 min)>), and the resulting hydrogenated block copolymer was added at the ratio shown in Tables 2 and 3, and 30
Melt kneading was carried out at a temperature of 220 ° C. with a twin screw extruder of mm to pelletize.
【0028】得られたペレットを230℃で射出成形
し、シートとテストピース(タンザク片)を作成し、低
温(−30℃)での耐衝撃性、曲げ弾性率を測定した。
また、ペレットを用いてMFRを測定した。The obtained pellets were injection-molded at 230 ° C. to prepare a sheet and a test piece (tanzaku piece), and the impact resistance and bending elastic modulus at low temperature (−30 ° C.) were measured.
Moreover, MFR was measured using the pellet.
【0029】[0029]
【表2】 [Table 2]
【0030】[0030]
【表3】 [Table 3]
【0031】[0031]
【実施例1〜7】表2に示す配合で各々の高分子量水素
添加ブロック共重合体(a)と低分子量水素添加ブロッ
ク共重合体(b)をブレンドし、さらにポリプロピレン
(M8619)を加えて組成物を作成した。測定結果を
表2に示した。これらは低温における耐衝撃性が優れ、
かつ剛性バランスも良く、さらに流動性も優れた組成物
であった。Examples 1 to 7 Each high molecular weight hydrogenated block copolymer (a) and low molecular weight hydrogenated block copolymer (b) were blended in the composition shown in Table 2, and polypropylene (M8619) was further added. A composition was made. The measurement results are shown in Table 2. These have excellent impact resistance at low temperatures,
In addition, the composition had a good rigidity balance and excellent fluidity.
【0032】以上に示した実施例は、全て本発明の構成
に含まれる組成物の例であり、優れた特性を有するポリ
オレフィン組成物である。その特性の優れている点は、
以下の比較例(表3)と比較することにより、一層明白
となろう。また、構造を規定した効果も明らかである。The above examples are all examples of compositions included in the constitution of the present invention, and are polyolefin compositions having excellent properties. The advantage of its characteristics is that
It will become more apparent by comparison with the following comparative example (Table 3). Also, the effect of defining the structure is clear.
【0033】[0033]
【比較例1,2】高分子量水素添加ブロック共重合体
(a)と低分子量水素添加ブロック共重合体(b)を併
用せずに、単独に用いた例であるが、低温での耐衝撃性
が劣る。[Comparative Examples 1 and 2] High-molecular-weight hydrogenated block copolymer (a) and low-molecular-weight hydrogenated block copolymer (b) are used alone without being used in combination, but the impact resistance at low temperature is low. Inferior in nature.
【0034】[0034]
【比較例3】高分子量水素添加ブロック共重合体(a)
と低分子量ブロック共重合体の比率が、本発明の範囲外
であったものの例である。耐衝撃性−剛性−流動性のバ
ランスが悪いことがわかる。Comparative Example 3 High molecular weight hydrogenated block copolymer (a)
And the low molecular weight block copolymer was outside the scope of the present invention. It can be seen that the balance of impact resistance-rigidity-fluidity is poor.
【0035】[0035]
【比較例4】(b)成分の分子量が本発明の範囲外であ
ったものの例であるが、低温での耐衝撃性が劣る。Comparative Example 4 This is an example in which the molecular weight of the component (b) was outside the range of the present invention, but the impact resistance at low temperature was poor.
【0036】[0036]
【比較例5,6】水素添加ブロック共重合体の水添前の
ビニル結合量が本発明の範囲外であったものの例であ
る。耐衝撃性が劣り、また物性のバランスが悪化する。
水素添加ブロック共重合体の水添前のビニル結合量の重
要性がわかる。[Comparative Examples 5 and 6] Examples in which the amount of vinyl bond before hydrogenation of the hydrogenated block copolymer was outside the range of the present invention. The impact resistance is poor and the balance of physical properties is poor.
The importance of the amount of vinyl bond before hydrogenation of the hydrogenated block copolymer is understood.
【0037】[0037]
【比較例7】本発明の実施例2と同じベースポリマーで
あって、水素添加していないブロック共重合体(b−
7)を用いた例である。耐衝撃性と剛性が著しく低下し
ていることがわかる。Comparative Example 7 The same base polymer as in Example 2 of the present invention, but without hydrogenation (b-
This is an example using 7). It can be seen that the impact resistance and rigidity are significantly reduced.
【0038】[0038]
【比較例8】総合の平均分子量が高過ぎ、本発明の範囲
外であったものの例である。耐衝撃性、剛性、流動性、
全ての面で劣ることがわかる。Comparative Example 8 This is an example in which the total average molecular weight was too high and was outside the scope of the present invention. Impact resistance, rigidity, fluidity,
It turns out that everything is inferior.
【0039】[0039]
【比較例9】本発明の実施例1と同じ水素添加ブロック
共重合体を用いたが、ポリプロピレンに対するブロック
共重合体の比率が多いため、曲げ弾性率が著しく低下
し、実用的でない。Comparative Example 9 The same hydrogenated block copolymer as that used in Example 1 of the present invention was used, but the flexural modulus was remarkably lowered and it was not practical because the ratio of the block copolymer to polypropylene was large.
【0040】[0040]
【発明の効果】本発明は、ポリオレフィン系樹脂と特定
構造の水素添加ブロック共重合体からなる組成物であ
り、衝撃強度、特に低温時における耐衝撃性と剛性のバ
ランス、流動加工性に優れている。本発明の組成物は、
安価であり、かつ射出成形、押出成形等通常の成形法で
製品が得られ、日用部品、包装材料から自動車内外装品
等の自動車部品まで広範囲に利用できるものであり、産
業上の利用価値は極めて大きい。INDUSTRIAL APPLICABILITY The present invention is a composition comprising a polyolefin resin and a hydrogenated block copolymer having a specific structure, and is excellent in impact strength, particularly in balance of impact resistance and rigidity at low temperature, and flow processability. There is. The composition of the present invention is
It is inexpensive and can be obtained by ordinary molding methods such as injection molding and extrusion molding, and can be widely used from daily parts and packaging materials to automobile parts such as automobile interior and exterior parts. Is extremely large.
Claims (1)
5〜50重量部 (2) (a)少なくとも2個のビニル芳香族化合物を
主体とする重合体ブロックAと少なくとも1個の共役ジ
エン化合物を主体とする重合体ブロックBを有し、その
共役ジエン部分の80%以上が水素添加され、水添前の
ビニル結合量が40〜60%であり、(b)よりも高分
子量の水素添加ブロック共重合体と(b)少なくとも2
個のビニル芳香族化合物を主体とする重合体ブロックC
と少なくとも1個の共役ジエン化合物を主体とする重合
体ブロックDを有し、その共役ジエン部分の80%以上
が水素添加され、水添前のビニル結合量が40〜60%
であり、数平均分子量が4.5万を越える水素添加ブロ
ック共重合体とからなり (a)がブロック共重合体中 10重量%以上40重量
%未満 (b)がブロック共重合体中 60重量%を越え90重
量%以下 (a)と(b)との数平均分子量の算術平均が50,0
00〜150,000である水素添加ブロック共重合体
5〜50重量部よりなるポリオレフィン組成物。1. (1) Polyolefin resin 9
5 to 50 parts by weight (2) (a) having at least two polymer blocks A mainly composed of vinyl aromatic compounds and at least one polymer block B mainly composed of conjugated diene compounds, and the conjugated diene 80% or more of the portion is hydrogenated, the vinyl bond amount before hydrogenation is 40 to 60%, and a hydrogenated block copolymer having a higher molecular weight than (b) and (b) at least 2
Polymer block C mainly composed of vinyl aromatic compounds
And a polymer block D mainly composed of at least one conjugated diene compound, 80% or more of the conjugated diene portion is hydrogenated, and the vinyl bond amount before hydrogenation is 40 to 60%.
And a hydrogenated block copolymer having a number average molecular weight of more than 45,000 (a) in the block copolymer is 10% by weight or more and less than 40% by weight (b) is 60% in the block copolymer % And 90% by weight or less, the arithmetic average of the number average molecular weights of (a) and (b) is 50.0.
A polyolefin composition comprising 5 to 50 parts by weight of a hydrogenated block copolymer of 0 to 150,000.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3295755A JP2513951B2 (en) | 1991-11-12 | 1991-11-12 | Polyolefin composition with excellent impact resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3295755A JP2513951B2 (en) | 1991-11-12 | 1991-11-12 | Polyolefin composition with excellent impact resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05163388A true JPH05163388A (en) | 1993-06-29 |
JP2513951B2 JP2513951B2 (en) | 1996-07-10 |
Family
ID=17824750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3295755A Expired - Lifetime JP2513951B2 (en) | 1991-11-12 | 1991-11-12 | Polyolefin composition with excellent impact resistance |
Country Status (1)
Country | Link |
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JP (1) | JP2513951B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0551494A (en) * | 1991-05-16 | 1993-03-02 | Asahi Chem Ind Co Ltd | Polyolefin composition |
JP2003276118A (en) * | 2002-03-22 | 2003-09-30 | Asahi Kasei Corp | Multilayer film |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58187442A (en) * | 1982-04-28 | 1983-11-01 | Asahi Chem Ind Co Ltd | Polyolefin polymeric composition |
JPS6057463A (en) * | 1983-09-08 | 1985-04-03 | Sanyo Electric Co Ltd | Automatic addition system of computer for demand of insurance |
JPH0551494A (en) * | 1991-05-16 | 1993-03-02 | Asahi Chem Ind Co Ltd | Polyolefin composition |
-
1991
- 1991-11-12 JP JP3295755A patent/JP2513951B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58187442A (en) * | 1982-04-28 | 1983-11-01 | Asahi Chem Ind Co Ltd | Polyolefin polymeric composition |
JPS6057463A (en) * | 1983-09-08 | 1985-04-03 | Sanyo Electric Co Ltd | Automatic addition system of computer for demand of insurance |
JPH0551494A (en) * | 1991-05-16 | 1993-03-02 | Asahi Chem Ind Co Ltd | Polyolefin composition |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0551494A (en) * | 1991-05-16 | 1993-03-02 | Asahi Chem Ind Co Ltd | Polyolefin composition |
JP2513958B2 (en) * | 1991-05-16 | 1996-07-10 | 旭化成工業株式会社 | Polyolefin composition |
JP2003276118A (en) * | 2002-03-22 | 2003-09-30 | Asahi Kasei Corp | Multilayer film |
Also Published As
Publication number | Publication date |
---|---|
JP2513951B2 (en) | 1996-07-10 |
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