JPS60238341A - Polypropylene resin composition - Google Patents
Polypropylene resin compositionInfo
- Publication number
- JPS60238341A JPS60238341A JP9192584A JP9192584A JPS60238341A JP S60238341 A JPS60238341 A JP S60238341A JP 9192584 A JP9192584 A JP 9192584A JP 9192584 A JP9192584 A JP 9192584A JP S60238341 A JPS60238341 A JP S60238341A
- Authority
- JP
- Japan
- Prior art keywords
- average particle
- particle size
- calcium carbonate
- mica
- resin composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 Polypropylene Polymers 0.000 title claims abstract description 23
- 239000004743 Polypropylene Substances 0.000 title claims abstract description 21
- 229920001155 polypropylene Polymers 0.000 title claims abstract description 21
- 239000011342 resin composition Substances 0.000 title claims description 10
- 239000002245 particle Substances 0.000 claims abstract description 35
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 26
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims abstract description 20
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 13
- 239000010445 mica Substances 0.000 claims abstract description 12
- 229910052618 mica group Inorganic materials 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 abstract description 12
- 239000012770 industrial material Substances 0.000 abstract description 3
- 239000011256 inorganic filler Substances 0.000 abstract description 3
- 229910003475 inorganic filler Inorganic materials 0.000 abstract description 3
- GBAAKJBGIFHUCA-UHFFFAOYSA-J [Ca++].[Co++].[O-]C([O-])=O.[O-]C([O-])=O Chemical compound [Ca++].[Co++].[O-]C([O-])=O.[O-]C([O-])=O GBAAKJBGIFHUCA-UHFFFAOYSA-J 0.000 abstract 1
- 238000002156 mixing Methods 0.000 description 11
- 229920005672 polyolefin resin Polymers 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 230000007423 decrease Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 229920000098 polyolefin Polymers 0.000 description 5
- 239000006087 Silane Coupling Agent Substances 0.000 description 4
- 229920001400 block copolymer Polymers 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- 229920001384 propylene homopolymer Polymers 0.000 description 4
- JBHRGAHUHVVXQI-UHFFFAOYSA-N 1-triethoxysilylpropan-1-amine Chemical compound CCO[Si](OCC)(OCC)C(N)CC JBHRGAHUHVVXQI-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- JNPCNDJVEUEFBO-UHFFFAOYSA-N 1-butylpyrrole-2,5-dione Chemical compound CCCCN1C(=O)C=CC1=O JNPCNDJVEUEFBO-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- XLYMOEINVGRTEX-ARJAWSKDSA-N Ethyl hydrogen fumarate Chemical compound CCOC(=O)\C=C/C(O)=O XLYMOEINVGRTEX-ARJAWSKDSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- UIERETOOQGIECD-ARJAWSKDSA-N angelic acid Chemical compound C\C=C(\C)C(O)=O UIERETOOQGIECD-ARJAWSKDSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 125000005822 ethenylethoxy group Chemical group [H]\[#6]([H])=[#6](\[H])C([H])([H])C([H])([H])[#8]-* 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- XLYMOEINVGRTEX-UHFFFAOYSA-N fumaric acid monoethyl ester Natural products CCOC(=O)C=CC(O)=O XLYMOEINVGRTEX-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-VIFPVBQESA-N trimethoxy-[3-[[(2r)-oxiran-2-yl]methoxy]propyl]silane Chemical compound CO[Si](OC)(OC)CCCOC[C@H]1CO1 BPSIOYPQMFLKFR-VIFPVBQESA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は衝撃強度にすぐれると共に剛性、熱変形温度が
高く自動車1弱電などの分野における工業材料として好
適なポリプロピレン樹脂組成物に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a polypropylene resin composition which has excellent impact strength, high rigidity and heat distortion temperature, and is suitable as an industrial material in fields such as automobiles and light electrical appliances.
(従来の技術)
熱可塑性樹脂、特にポリオレフィン系樹脂の剛性1機械
的強度等を向上させるために1マイカを充填することが
行なわれている(特公昭58−17544号、特公昭5
8−17545号)。しかしながら、ポリオレフィン系
樹脂にマイカを充填すると、衝撃強度が著しく低下する
という大きな欠点がある。(Prior art) In order to improve the rigidity, mechanical strength, etc. of thermoplastic resins, especially polyolefin resins, it has been carried out to fill them with mica.
No. 8-17545). However, when polyolefin resin is filled with mica, there is a major drawback in that impact strength is significantly reduced.
このような衝撃強度の低下を改善するために、さらにゴ
ムを配合することも提案されているが、剛性、熱変形温
度が低下するという問題が発生するなど、未だ充分に満
足しつるものは得られていない。In order to improve this reduction in impact strength, it has been proposed to add more rubber to the mix, but this has not yet been fully satisfactory due to problems such as a decrease in rigidity and heat distortion temperature. It has not been done.
(発明が解決しようとする問題点)
本発明者らは上記従来の欠点を解消すべく鋭意研究を取
ねた結果、結晶性ポリプロピレンに所定の範囲の平均粒
子径を有する特定の無機充填剤をマイカとともに配合す
ると剛性および熱変形温度が向上し、かつ大幅に衝撃強
度が向上することを見出し、本発明を完成するに到った
。(Problems to be Solved by the Invention) The present inventors have conducted intensive research to solve the above-mentioned conventional drawbacks, and as a result, we have found that a specific inorganic filler having an average particle diameter within a predetermined range is added to crystalline polypropylene. The present inventors have discovered that when blended with mica, the rigidity and heat distortion temperature are improved, and the impact strength is significantly improved, and the present invention has been completed.
(問題点を解決するための手段)
すなわち本発明は、(4)結晶性ポリプロピレン(以下
、(A)成分という。)40〜90重量%、■)マイカ
(以下、Φ)成分という。)および(Q平均粒子径0.
05〜0.8μの炭酸カルシウムまたは平均粒子径0・
1〜0.9μの硫酸バリウム(以下、(C)成分という
。)5〜40重量%よりなるポリプロピレン樹脂組成物
を提供するものである。(Means for Solving the Problems) That is, the present invention consists of (4) crystalline polypropylene (hereinafter referred to as component (A)) of 40 to 90% by weight, and ■) mica (hereinafter referred to as Φ) component. ) and (Q average particle size 0.
Calcium carbonate of 05-0.8μ or average particle size 0.
The present invention provides a polypropylene resin composition comprising 5 to 40% by weight of barium sulfate (hereinafter referred to as component (C)) having a particle size of 1 to 0.9μ.
本発明において(4)成分として用いる結晶性ポリプロ
ピレンには各種のものが包含され、例えばプロピレンホ
モポリマー、プロピレンとエチレンなどの他の共重合成
分とのブロックコポリマー、ランダムコポリマーがあり
、とりわけプロピレン−エチレンブロックコポリマーや
プロピレンホモポリマーが好ましい。この結晶性ポリプ
ロピレンのメルトインデックス(MI)は1〜60 、
F /10分、好ましくは2〜1077710分である
。The crystalline polypropylene used as component (4) in the present invention includes various types, such as propylene homopolymers, block copolymers and random copolymers of propylene and other copolymer components such as ethylene, and especially propylene-ethylene copolymers. Block copolymers and propylene homopolymers are preferred. The melt index (MI) of this crystalline polypropylene is 1 to 60,
F/10 minutes, preferably 2-1077710 minutes.
ここで結晶性ポリプロピレンの配合割合は組成物全体の
40〜90取量%、姓ましくは60〜80改量%である
。結晶性ポリプロピレンの配合割合が40重量%未満で
あると、流動性の低下が起こり好ましくないっ一方、9
0重量%を超えると、剛性、熱変形温度などの改良効果
が不十分となるので好ましくない。Here, the blending ratio of crystalline polypropylene is 40 to 90% by weight, preferably 60 to 80% by weight of the entire composition. If the blending ratio of crystalline polypropylene is less than 40% by weight, fluidity will decrease, which is undesirable;
If it exceeds 0% by weight, the effects of improving stiffness, heat distortion temperature, etc. will be insufficient, which is not preferable.
次に本発明においてはCB)成分としてマイカを用いる
。このマイカとしてはアスペクト比が5〜120、好ま
しくは30〜70のものが用いられる。また、平均粒子
径が5〜250μのものが好・fしく用いられる。ここ
で平均粒子径が5μ未満のものであると、剛性の改良効
果が小さい。一方、平均粒子径が250μを超えたもの
であると、組成物の表面外観が悪化する。なお、(B)
成分としては7ランカツプリング剤で処理されたマイカ
を用いることがより好ましい。このようなシランカップ
リング剤で処理することにより親和性を向上させること
ができる。ここでシランカップリング剤としては様々な
ものがあり、例えばビニルエトキ7ノラン、ビニルトリ
クロロシラン、ビニルトリス(β−メトキシエトキシ7
ラン)、r−グリシドキシプロピルトリメトキシシラン
、α−アミノプロピルトリエトキシシラン、r−アミノ
プロピルトリエトキシシラン、r−メタクリーロキシプ
ロピルトリメトキシシラン、N−β−(アミノエチル)
−r−アミノプロピルトリエトキクシラン。Next, in the present invention, mica is used as the component CB). The mica used has an aspect ratio of 5 to 120, preferably 30 to 70. Moreover, those having an average particle diameter of 5 to 250 μm are preferably used. Here, if the average particle diameter is less than 5 μm, the effect of improving rigidity is small. On the other hand, if the average particle diameter exceeds 250μ, the surface appearance of the composition deteriorates. Furthermore, (B)
As a component, it is more preferable to use mica treated with a 7-run coupling agent. Affinity can be improved by treatment with such a silane coupling agent. There are various silane coupling agents, such as vinyl ethoxy 7-nolan, vinyl trichlorosilane, vinyl tris (β-methoxyethoxy 7
Ran), r-glycidoxypropyltrimethoxysilane, α-aminopropyltriethoxysilane, r-aminopropyltriethoxysilane, r-methacryloxypropyltrimethoxysilane, N-β-(aminoethyl)
-r-aminopropyltriethoxysilane.
N−ビス−(β−ヒドロキシエチル)−r−アミノプロ
ピルトリエトキシシラン、N−β−(アミノエチ/I/
) −1−アミノプロピルメチルジェトキシシランな
どを挙げることができ、これらの中でもアミノ基を有す
る化合物を用いることが好ましい。このシランカップリ
ング剤での処理は通常0.5〜5重量%のシランカップ
リング剤を用いて行なう。N-bis-(β-hydroxyethyl)-r-aminopropyltriethoxysilane, N-β-(aminoethyl/I/
) -1-Aminopropylmethyljethoxysilane, etc. Among these, it is preferable to use a compound having an amino group. This treatment with a silane coupling agent is usually carried out using 0.5 to 5% by weight of the silane coupling agent.
03)成分の配合割合は組成物全体の5〜40取量%、
好ましくは10〜301目である。ここで(至))成分
の配合割合が5重量%未満であると剛性。03) The blending ratio of the ingredients is 5 to 40% of the total composition,
Preferably the number is 10 to 301. (to) If the blending ratio of the components is less than 5% by weight, the stiffness will be reduced.
寸法の改良効果が小さくなり、一方4 o *m%を超
えると流動性゛の低下9表面外観の低下が起こり好まし
くない。The dimensional improvement effect becomes small, and on the other hand, if it exceeds 4 o * m%, the fluidity decreases and the surface appearance deteriorates, which is not preferable.
さらに1本発明においては(C)成分として平均粒子径
0゜05〜0.8μの炭酸カルシウムまたは平均粒子径
0.1〜0.9μの硫酸バリウムを用いる。Furthermore, in the present invention, calcium carbonate having an average particle diameter of 0.05 to 0.8 .mu.m or barium sulfate having an average particle diameter of 0.1 to 0.9 .mu.m is used as component (C).
(0)成分として炭酸カルシウムを用いる場合、平均粒
子滓が0.05〜0.8μのものを用いることが必要で
あり、特に平均粒子径が0.1〜0.6μのコロイド炭
酸カルシウムを用いることが好ましいOここで炭酸カル
シウムの平均粒子径が0.8μを超えたものであると、
衝撃強度が低下し、0.05μ未満のものであると、分
散が充分でなく衝撃強度の改良効果がみられず好ましく
ない。When using calcium carbonate as component (0), it is necessary to use one with an average particle size of 0.05 to 0.8 μm, and in particular, use colloidal calcium carbonate with an average particle size of 0.1 to 0.6 μm. It is preferred that the average particle size of the calcium carbonate exceeds 0.8μ,
The impact strength decreases, and if it is less than 0.05 μm, the dispersion is insufficient and no impact strength improvement effect is observed, which is not preferable.
一方、(C)成分として硫酸バリウムを用いる場合、平
均粒子径が0゜1〜0.9μのものを用いることが必要
であり、特に平均粒子径が0.3〜0゜9μのものを用
いることが好ましい。ここで硫酸バリウムの平均粒子径
が帆9μを超えたものであると衝撃強度が低下し、一方
O01μ未満のものであると分散が充分でなく衝撃強度
の改良効果がみられないので好ましくない。On the other hand, when barium sulfate is used as component (C), it is necessary to use one with an average particle size of 0°1 to 0.9μ, particularly one with an average particle size of 0.3 to 0°9μ. It is preferable. If the average particle diameter of barium sulfate exceeds 9μ, the impact strength will decrease, while if it is less than 001μ, the dispersion will be insufficient and no impact strength improvement effect will be seen, which is not preferred.
本発明において(0)成分としては上記特定の範囲の平
均粒子径を有する炭酸カルシウムあるいは硫酸バリウム
を用いることが必要であって、これら三者以外のもの、
あるいはこれら三者のうちのいずれかであっても上記特
定の範囲の平均粒子径を有しないものを用いた場合には
本発明の所期の目的を達成することは不可能である。In the present invention, as component (0), it is necessary to use calcium carbonate or barium sulfate having an average particle size within the above specified range, and other than these three,
Alternatively, if any one of these three particles does not have an average particle diameter within the above-mentioned specific range, it is impossible to achieve the intended purpose of the present invention.
(0)成分の配合割合は組成物全体の5〜40取量%、
好ましくは10〜30取量%である。ここで(0)成分
の配合割合が51Effi%未満であると、衝撃強度の
改良効果が小さく、一方40重量%を超えると、流動性
の低下が起こり好ましくない。(0) The blending ratio of the ingredients is 5 to 40% of the total composition,
Preferably it is 10-30%. If the blending ratio of component (0) is less than 51% by weight, the effect of improving impact strength will be small, while if it exceeds 40% by weight, fluidity will deteriorate, which is undesirable.
本発明は基本的には上記(4)、 CB) 、 (0)
の3成分よりなるものであるが、さらに必要により不飽
和カルボン酸またはその誘導体で変性されたポリオレフ
ィン樹脂を配合することもできる。ここで不飽和カルボ
ン酸またはその誘導体で変性されたポリオレフィン樹脂
とは不飽和カルボン酸またはその誘導体によって変性さ
れたポリオレフィン樹脂あるいは該変性ポリオレフィン
樹脂と未変性ポリオレフィン樹脂との混合物を意味し、
ポリオレフィン樹脂としてはプロピレンホモポリマー、
プロピレンとエチレンなどの他の共重合成分とのブロッ
クコポリマー、ランダムコポリマーなどのポリプロピレ
ン系樹脂が好ましい。また、不飽和カルボ/酸としては
アクリル酸、メタアクリル酸、マレイン酸、フマル酸、
イタコン酸、クロトン酸、シトラコン酸、ソルビン酸、
メサコン酸、アンゲリカ酸などがある。また、その誘導
体としては、酸無水物、エステル、アミド、イミド、金
属塩などがあり、例えば無水マレイン酸、無水イタコン
酸。The present invention basically consists of the above (4), CB), and (0).
However, if necessary, a polyolefin resin modified with an unsaturated carboxylic acid or a derivative thereof may be added. Here, the polyolefin resin modified with an unsaturated carboxylic acid or a derivative thereof means a polyolefin resin modified with an unsaturated carboxylic acid or a derivative thereof, or a mixture of the modified polyolefin resin and an unmodified polyolefin resin,
As polyolefin resin, propylene homopolymer,
Polypropylene resins such as block copolymers and random copolymers of propylene and other copolymer components such as ethylene are preferred. In addition, unsaturated carboxylic acids include acrylic acid, methacrylic acid, maleic acid, fumaric acid,
itaconic acid, crotonic acid, citraconic acid, sorbic acid,
These include mesaconic acid and angelic acid. Further, its derivatives include acid anhydrides, esters, amides, imides, metal salts, etc., such as maleic anhydride and itaconic anhydride.
無水シトラコン酸、アクリルばメチル、メタアクリル醒
メチル、アクリル酸エチル、アクリル酸ブチル、マレイ
ン酸モノエチルエステル、アクリルアミド、−yレイン
酸モノアミド、マレイミド、N−ブチルマレイミド、ア
クリル酸ナトリウム、メタアクリル酸ナトリウムなどを
挙げることができる。これらの中では無水マレイン酸が
好適である0これらの不飽和カルボン酸またはその誘導
体によってポリオレフィンを変性するには、その方法は
特に制限されず、公知の種々の方法を用いて行なうこと
ができる。例えばポリオレフィンと無水マレイン酸等を
溶媒の存在下あるいは不存在下でラジカル開始剤を添加
し、加熱することにより行なう。反応に際しては、スチ
レンなどの他のとニルモノマーあるいは液状ゴム、熱可
塑性ゴムなどのゴム類を共存させることもできる。ここ
で変性ポリオレフィンとしては酸付加量が0.5〜10
重量%のものが好ましい。Citraconic anhydride, methyl acrylate, methyl methacrylate, ethyl acrylate, butyl acrylate, monoethyl maleate, acrylamide, -yleic acid monoamide, maleimide, N-butylmaleimide, sodium acrylate, sodium methacrylate etc. can be mentioned. Among these, maleic anhydride is preferred.The method for modifying polyolefins with these unsaturated carboxylic acids or derivatives thereof is not particularly limited, and various known methods can be used. For example, this is carried out by adding a radical initiator to polyolefin and maleic anhydride in the presence or absence of a solvent and heating the mixture. During the reaction, other monomers such as styrene or rubbers such as liquid rubber and thermoplastic rubber may also be present. Here, the modified polyolefin has an acid addition amount of 0.5 to 10
% by weight is preferred.
この変性ポリオレフィンを上記(4)、 CB) 、
(0)成分の総和100重量部に対してO65〜5取量
部添加することによりさらに機械的強度を向上させるこ
とができる0本発明の組成物にはさらに必要に応じて各
種の添bn剤、例えばば化防止剤、紫外線吸収剤、帯電
防止剤等を適宜添加することもできる。This modified polyolefin is processed into the above (4), CB),
(0) Mechanical strength can be further improved by adding 65 to 5 parts of O to 100 parts by weight of the total components.0 The composition of the present invention may also contain various additives as necessary. For example, an anti-fog agent, an ultraviolet absorber, an antistatic agent, etc. may be added as appropriate.
本発明のポリプロピレン樹脂組成物は上記各成分を所定
量配合し、乾湿・融混併用法、多段溶融混合法、単純溶
融混合法等によって充分に混練することにより得ること
ができる。なお、混線はノくンバリーミキサー、コニー
ダー、押出機、二軸混練機等を用いて常法により行なう
ことができ、通常180〜250℃の温度で行なわれる
。The polypropylene resin composition of the present invention can be obtained by blending the above-mentioned components in predetermined amounts and sufficiently kneading the mixture by a dry/wet/melt mixing method, a multistage melt mixing method, a simple melt mixing method, or the like. The mixing can be carried out in a conventional manner using a Nokunbury mixer, a co-kneader, an extruder, a twin-screw kneader, etc., and is usually carried out at a temperature of 180 to 250°C.
(発明の効果)
本発明のポリプロピレン樹脂組成物は、特定範囲の平均
粒径を有する特定の無機充填剤を配合しているため、従
来のものに比し一層衝撃強変のすz8引−ナー ぬ n
)−ra ム 六 〜しかも、本発明のポリプロピレン
樹脂組成物G家剛性、熱変形温度にもすぐれたものであ
る。(Effects of the Invention) Since the polypropylene resin composition of the present invention contains a specific inorganic filler having an average particle size within a specific range, it can be used as a Z8 binder with higher impact resistance than conventional ones. Nu n
In addition, the polypropylene resin composition of the present invention has excellent rigidity and heat distortion temperature.
したがって本発明のポリプロピレン樹脂組成物は自動車
1弱電などの分野における工業材料として有効に利用す
ることができる。Therefore, the polypropylene resin composition of the present invention can be effectively used as an industrial material in fields such as automobiles and light electrical appliances.
(実施例) 次に本発明の実施例を示す。(Example) Next, examples of the present invention will be shown.
実施例1〜10および比較例1〜10
所定の結晶性ポリプロピレン((A)成分)、マイカ(
(B)成分)、所定の粒子径を有する炭酸カルシウムま
たは硫酸バリウム((C)成分)および変性ポリオレフ
ィンを第1表に示す割合で配合し、トライブレンドした
のち二軸混練機を用いて混練し樹脂組成物を得た。得ら
れた組成物の物性の測定結果を第1表に示す。Examples 1 to 10 and Comparative Examples 1 to 10 Predetermined crystalline polypropylene (component (A)), mica (
(B) component), calcium carbonate or barium sulfate having a predetermined particle size ((C) component), and modified polyolefin are blended in the proportions shown in Table 1, triblended, and then kneaded using a twin-screw kneader. A resin composition was obtained. Table 1 shows the measurement results of the physical properties of the obtained composition.
注)
a:プロピレン−エチレンブロック共重合体(MI 6
g710分、エチレン含有量9重量%)b:プロピレン
ホモポリマ−(MI ag/lo分)C:平均粒子径9
0μ、アスペクト比50のマイカをα−アミノプロピル
トリエトキシシランで処理したもの
d:平均粒子径40μ、アスペクト比30のマイカ
e:平均粒子径0.15μのコロイド炭酸カルシウム
f:平均粒子径0.6μのコロイド炭酸カルシウム
g:平均粒子径0.6μの沈降性硫酸バリウ=ムh:平
均粒子径3.8μの重質炭酸カルシウム1:平均粒子径
0.03μのコロイド炭酸カルシウム
j:平均粒子径4.6μの硫酸バリウム*1:無水マレ
イン酸で変性したポリプロピレン(#付加量5取量%)
*2 : AS’l’M D256 (ノツチ付)に準
拠*3 : A8TM D638に準拠
*4 : A8TM D 790に準拠*5 : A8
TM D 648 (荷重18.6騰んi)に準拠*6
:エチレンープロピレンゴム
(ムーニー粘度風、+4(100) 24 )特許出願
人 出光石油化学株式会社
手続補正書(自発)
昭和59年 6月夏8日
特許庁長官 若杉和夫 殿
1、事件の表示
特願昭54L−91925
2、発明の名称
ポリプロピレン樹脂組成物
3、補正をする者
事件との関係 特許出願人
出光石油化学株式会社
4、代理人
■104
住所 東京都中央区京橋1丁目1番10号西勘ビル5階
氏名 (7407)弁理士 久保1)藤6部電話(27
5)0721番
5、補正の対象
6、補正の内容
(1)明細書第4真下から5〜4行目の「α−アミ、ノ
プロビルトリエトキシシラン、」を削除する。Note) a: Propylene-ethylene block copolymer (MI 6
g710 min, ethylene content 9% by weight) b: Propylene homopolymer (MI ag/lo min) C: average particle size 9
d: Mica with an average particle size of 40μ and an aspect ratio of 30 treated with α-aminopropyltriethoxysilane e: Colloidal calcium carbonate with an average particle size of 0.15μ f: Average particle size of 0.0μ and an aspect ratio of 50 treated with α-aminopropyltriethoxysilane. 6μ colloidal calcium carbonate g: precipitated barium sulfate mu with average particle size 0.6μ h: ground calcium carbonate with average particle size 3.8μ 1: colloidal calcium carbonate with average particle size 0.03μ j: average particle size 4.6μ barium sulfate *1: Polypropylene modified with maleic anhydride (# added amount: 5%) *2: Based on AS'l'M D256 (with notch) *3: Based on A8TM D638 *4: Compliant with A8TM D 790 *5: A8
Compliant with TM D 648 (load 18.6 rise) *6
: Ethylene-propylene rubber (Mooney viscosity wind, +4 (100) 24) Patent applicant: Idemitsu Petrochemical Co., Ltd. Procedural amendment (spontaneous) June 8, 1981 Commissioner of the Japan Patent Office Kazuo Wakasugi 1, Indication special of the case Application No. 54L-91925 2. Name of the invention Polypropylene resin composition 3. Relationship with the case by the person making the amendment Patent applicant Idemitsu Petrochemical Co., Ltd. 4. Agent ■104 Address 1-1-10 Kyobashi, Chuo-ku, Tokyo Nishikan Building 5th Floor Name (7407) Patent Attorney Kubo 1) Fuji 6th Department Telephone (27)
5) No. 0721 No. 5, Target of correction 6, Contents of correction (1) Delete "α-amino, noprobiltriethoxysilane," in lines 5 to 4 from the bottom of No. 4 of the specification.
(2)同ff1l Z頁6〜7行目の[α−アミノプロ
ピルトリエトキシシラン」を「γ−アミノプロピルトリ
エトキシシラン」に訂正する。(2) Correct [α-aminopropyltriethoxysilane] in lines 6 and 7 on page Z of the same ff1l to “γ-aminopropyltriethoxysilane”.
(以上)(that's all)
Claims (1)
0605〜0.8μの炭酸カルシウムまたは平均粒子径
0.1〜0.9μの硫酸バリウム5〜401目よりなる
ポリプロピレン樹脂組成物。[Claims] 1. (A) 40 to 90% by weight of crystalline polypropylene. A polypropylene resin composition comprising (to) 5 to 30% by weight of mica and (0) calcium carbonate having an average particle size of 0605 to 0.8 μm or barium sulfate having an average particle size of 0.1 to 0.9 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9192584A JPS60238341A (en) | 1984-05-10 | 1984-05-10 | Polypropylene resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9192584A JPS60238341A (en) | 1984-05-10 | 1984-05-10 | Polypropylene resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60238341A true JPS60238341A (en) | 1985-11-27 |
| JPS649339B2 JPS649339B2 (en) | 1989-02-17 |
Family
ID=14040158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9192584A Granted JPS60238341A (en) | 1984-05-10 | 1984-05-10 | Polypropylene resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60238341A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1091121C (en) * | 1996-12-31 | 2002-09-18 | 南京熊猫电子股份有限公司 | High elastic modified polypropylene material and its prepn. method |
| EP1347010A1 (en) * | 2002-03-22 | 2003-09-24 | Fort James Corporation | Thermoformed food containers with enhanced rigidity |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4916553A (en) * | 1972-06-06 | 1974-02-14 | ||
| JPS5521494A (en) * | 1978-07-31 | 1980-02-15 | Bethlehem Steel Corp | Olefin composition having high antiishock and high temperature flow resistance and metal plastic laminate obtained therefrom |
-
1984
- 1984-05-10 JP JP9192584A patent/JPS60238341A/en active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4916553A (en) * | 1972-06-06 | 1974-02-14 | ||
| JPS5521494A (en) * | 1978-07-31 | 1980-02-15 | Bethlehem Steel Corp | Olefin composition having high antiishock and high temperature flow resistance and metal plastic laminate obtained therefrom |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1091121C (en) * | 1996-12-31 | 2002-09-18 | 南京熊猫电子股份有限公司 | High elastic modified polypropylene material and its prepn. method |
| EP1347010A1 (en) * | 2002-03-22 | 2003-09-24 | Fort James Corporation | Thermoformed food containers with enhanced rigidity |
| US6881937B2 (en) | 2002-03-22 | 2005-04-19 | Fort James Corporation | Thermoformed food containers with enhanced rigidity |
| US7482053B2 (en) | 2002-03-22 | 2009-01-27 | Dixie Consumer Products Llc | Thermoformed food containers with enhanced rigidity |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS649339B2 (en) | 1989-02-17 |
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