JP2695492B2 - Polyamide / polyolefin resin composition - Google Patents
Polyamide / polyolefin resin compositionInfo
- Publication number
- JP2695492B2 JP2695492B2 JP28478589A JP28478589A JP2695492B2 JP 2695492 B2 JP2695492 B2 JP 2695492B2 JP 28478589 A JP28478589 A JP 28478589A JP 28478589 A JP28478589 A JP 28478589A JP 2695492 B2 JP2695492 B2 JP 2695492B2
- Authority
- JP
- Japan
- Prior art keywords
- polyamide
- resin
- ethylene
- copolymer
- weight
- 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.)
- Expired - Fee Related
Links
- 229920006122 polyamide resin Polymers 0.000 title claims description 29
- 239000011342 resin composition Substances 0.000 title claims description 20
- 239000004952 Polyamide Substances 0.000 title claims description 17
- 229920005672 polyolefin resin Polymers 0.000 title claims description 9
- 239000004743 Polypropylene Substances 0.000 claims description 32
- -1 Polypropylene Polymers 0.000 claims description 28
- 229920001155 polypropylene Polymers 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 23
- 239000011347 resin Substances 0.000 claims description 23
- 229920000098 polyolefin Polymers 0.000 claims description 15
- 239000000155 melt Substances 0.000 claims description 8
- 238000000465 moulding Methods 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 description 29
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 16
- 239000005977 Ethylene Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 229920002647 polyamide Polymers 0.000 description 11
- 238000002156 mixing Methods 0.000 description 8
- 238000004898 kneading Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N fumaric acid group Chemical group C(\C=C\C(=O)O)(=O)O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920001384 propylene homopolymer Polymers 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 229920000305 Nylon 6,10 Polymers 0.000 description 2
- 229920000572 Nylon 6/12 Polymers 0.000 description 2
- 229920000577 Nylon 6/66 Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- TZYHIGCKINZLPD-UHFFFAOYSA-N azepan-2-one;hexane-1,6-diamine;hexanedioic acid Chemical compound NCCCCCCN.O=C1CCCCCN1.OC(=O)CCCCC(O)=O TZYHIGCKINZLPD-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920000573 polyethylene 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
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- 229920012753 Ethylene Ionomers Polymers 0.000 description 1
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-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
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920000393 Nylon 6/6T Polymers 0.000 description 1
- 229920002614 Polyether block amide Polymers 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical group CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000004018 acid anhydride group Chemical group 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- ZMUCVNSKULGPQG-UHFFFAOYSA-N dodecanedioic acid;hexane-1,6-diamine Chemical compound NCCCCCCN.OC(=O)CCCCCCCCCCC(O)=O ZMUCVNSKULGPQG-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical group OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229920001912 maleic anhydride grafted polyethylene Polymers 0.000 description 1
- 229920001911 maleic anhydride grafted polypropylene Polymers 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000004492 methyl ester group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical group CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 229920006012 semi-aromatic polyamide Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001567 vinyl ester resin Chemical group 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明はポリアミド・ポリオレフィン樹脂組成物に関
し、詳しくは、ポリアミド樹脂とポリプロピレン樹脂の
それぞれの優れた特性を併せ有し、特に塗装性に優れた
ポリアミド・ポリオレフィ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 polyamide / polyolefin resin composition, and more specifically, it has excellent characteristics of both polyamide resin and polypropylene resin, and is particularly excellent in coatability. The present invention relates to a polyamide / polyolefin resin composition.
一般に、ポリアミド樹脂は、物理的,化学的性質に優
れていることから合成繊維などとして幅広く利用されて
いるが、近年成形材料としても利用されるようになって
いる。これは、ポリアミド樹脂が熱可塑性樹脂の中にあ
って、高い機械的強度,優れた耐摩耗性,耐薬品性,耐
熱性及び比較的優れた電気的性質を有し、エンジニアリ
ングプラスチックとしての性能を充分有していることに
よる。しかし、その反面、アミド基(−CONH−)に起因
して吸水による寸法変化や機械的強度の低下が生ずるな
どの好ましからざる性能を有しており、それが故に、成
形材料としての市場性が限定されている。Generally, a polyamide resin is widely used as a synthetic fiber or the like because of its excellent physical and chemical properties, but in recent years, it has also been used as a molding material. This is because the polyamide resin is a thermoplastic resin, has high mechanical strength, excellent wear resistance, chemical resistance, heat resistance and relatively excellent electrical properties, and has performance as an engineering plastic. It depends on having enough. However, on the other hand, it has unfavorable performance such as dimensional change due to water absorption and deterioration of mechanical strength due to the amide group (-CONH-), which makes it marketable as a molding material. Limited.
一方、ポリプロピレン樹脂は安価で、かつ吸水性はほ
とんど示さないが、軟質であり、高温時の物性が劣るな
どの欠点がある。On the other hand, polypropylene resin is inexpensive and exhibits almost no water absorbency, but it has drawbacks such as softness and poor physical properties at high temperatures.
したがって、ポリアミド樹脂およびポリプロピレン樹
脂のそれぞれの欠点を改善するために、これらの樹脂を
併用することは当然考えられるが、ポリアミド樹脂とポ
リプロピレン樹脂を通常の方法で混合して得た樹脂混合
物、あるいはそれらを単に溶融混練して得た樹脂組成物
では相溶性が劣り、目的とする優れた物性を持つ組成物
とはなりえない。Therefore, in order to improve the respective drawbacks of the polyamide resin and the polypropylene resin, it is naturally conceivable to use these resins together, but a resin mixture obtained by mixing the polyamide resin and the polypropylene resin by a usual method, or those The resin composition obtained by simply melt-kneading is poor in compatibility and cannot be a composition having the desired excellent physical properties.
そのため、従来からポリアミド樹脂とポリプロピレン
樹脂のそれぞれの優れた特性を併せ有する樹脂組成物、
すなわちポリアミド樹脂が有する優れた耐摩耗性,電気
特性,耐熱性,機械的強度,耐油性、さらにポリプロピ
レン樹脂が有する低吸水性,耐熱水性,耐ハロゲン化金
属性,低温耐衝撃性を併せ有する樹脂組成物を得ること
を目的として、ポリアミド樹脂,オルフィン重合体及び
不飽和カルボン酸またはその誘導体をグラフトした変性
ポリオレフィンの三成分を溶融混合して、強度,耐熱変
形性,外観,成形加工性のバランスが優れた組成物を得
ることについては、すでに特公昭42−12546号公報,特
公昭45−30945号公報,特公昭50−7636号公報などに示
されている。また、このような優れた性質を利用して、
自動車部品,電機器具,機械部品,工業部品などの強度
や耐熱変形性の要求される用途で実用化が検討された
り、一部では実用化がなされている。Therefore, conventionally, a resin composition having both excellent properties of polyamide resin and polypropylene resin,
That is, a resin that has the excellent wear resistance, electrical characteristics, heat resistance, mechanical strength, and oil resistance of a polyamide resin, as well as the low water absorption, hot water resistance, metal halide resistance, and low temperature impact resistance of a polypropylene resin. For the purpose of obtaining a composition, a polyamide resin, an olfine polymer, and a modified polyolefin grafted with an unsaturated carboxylic acid or a derivative thereof are melt-mixed to obtain a balance of strength, heat distortion resistance, appearance, and moldability. Has already been disclosed in JP-B-42-12546, JP-B-45-30945, JP-B-50-7636 and the like. In addition, by utilizing such excellent properties,
Practical applications are being considered for some applications, such as automobile parts, electrical appliances, mechanical parts, and industrial parts, which require strength and heat distortion resistance, and some have already been put into practical use.
しかしながら、このような特徴を有する樹脂組成物
(ポリマーアロイ組成物)であっても、塗装性が未だ充
分でないという問題がある。これらのポリマーアロイ組
成物には、ポリアミド樹脂に比べて塗装性の悪いポリプ
ロピレン樹脂が含まれるため、かなり用途が限定されて
いるのが現状である。However, even a resin composition (polymer alloy composition) having such characteristics has a problem that the coatability is still insufficient. These polymer alloy compositions contain polypropylene resins, which have poorer coatability than polyamide resins, so that their applications are currently limited.
本発明者らは、ポリアミド樹脂ならびにポリプロピレ
ン樹脂の優れた特性を維持しつつ、特に塗装性を改良す
ることを目的として鋭意研究を重ねた。その結果、成形
加工温度における溶融粘度の比が一定の関係にあるポリ
アミド樹脂とポリプロピレン樹脂を適宜組み合わせて用
いるとともに、変性ポリオレフィンとともに配合するこ
とにより、目的を達成できることを見出した。The inventors of the present invention have conducted intensive studies to maintain the excellent properties of polyamide resins and polypropylene resins while improving the paintability. As a result, they have found that the object can be achieved by appropriately combining and using a polyamide resin and a polypropylene resin having a constant relationship of the melt viscosity at the molding processing temperature, and by compounding them together with a modified polyolefin.
本発明は、かかる知見に基いて完成したものである。
すなわち本発明は、 (A)ポリアミド樹脂80〜40重量%(但し、40重量%を
除く。), (B)変性ポリオレフィン1〜40重量%及び (C)ポリプロピレン樹脂20〜60重量%からなり、かつ
成形加工温度,剪断速度3500sec-1における前記(A)
ポリアミド樹脂の溶融粘度ηPA(poise)と(C)ポリ
プロピレン樹脂の溶融粘度ηPP(poise)の比が、 式 ηPP/ηPA>0.75 ・・・〔I〕 を満たすことを特徴とするポリアミド・ポリオレフィン
樹脂組成物を提供するものである。The present invention has been completed based on such findings.
That is, the present invention comprises (A) polyamide resin 80 to 40% by weight (excluding 40% by weight), (B) modified polyolefin 1 to 40% by weight and (C) polypropylene resin 20 to 60% by weight, Moreover, the above (A) at a molding processing temperature and a shear rate of 3500 sec -1
A polyamide characterized in that the ratio of the melt viscosity η PA (poise) of the polyamide resin and the melt viscosity η PP (poise) of the (C) polypropylene resin satisfies the formula η PP / η PA > 0.75 ... [I] -Providing a polyolefin resin composition.
本発明に用いる(A)ポリアミド樹脂としては各種の
ものが使用可能であるが、具体的にはナイロン6,ナイロ
ン11,ナイロン12などのポリラクタム類;ナイロン66,ナ
イロン610,ナイロン612,ナイロン46等のジカルボン酸と
ジアミンとから得られるポリアミド類;ナイロン6/66,
ナイロン6/12,ナイロン6/66/610等の共重合体ポリアミ
ド類;ナイロン6/6T(T:テレフタル酸成分),イソフタ
ル酸のような芳香族ジカルボン酸とメタキシレンジアミ
ンあるいは脂環族ジアミンから得られる半芳香族ポリア
ミド類;ポリエステルアミド,ポリエーテルアミド及び
ポリエステルエーテルアミドを挙げることができる。な
お、(A)成分のポリアミド樹脂としては、上記各種の
ポリアミドを単独で用いてもよく、また二種以上のポリ
アミドを併用することもできる。As the (A) polyamide resin used in the present invention, various types can be used, but specifically, polylactams such as nylon 6, nylon 11, nylon 12; nylon 66, nylon 610, nylon 612, nylon 46, etc. Polyamides obtained from dicarboxylic acids and diamines; nylon 6/66,
Copolymer polyamides such as nylon 6/12, nylon 6/66/610; from aromatic dicarboxylic acids such as nylon 6 / 6T (T: terephthalic acid component), isophthalic acid and metaxylene diamine or alicyclic diamine The semi-aromatic polyamides obtained may include polyester amides, polyether amides and polyester ether amides. As the polyamide resin as the component (A), the above various polyamides may be used alone, or two or more kinds of polyamides may be used in combination.
さらに、本発明において使用できるポリアミド樹脂
は、上述のポリアミドより選択されたものであれば、こ
れらのポリアミドの末端基の種類や濃度および分子量な
どにより制限されることなく種々のものを使用すること
ができるが、とりわけ高アミノ未端ポリアミドが好まし
い。また、ポリアミドの重合時に残存または生成するモ
ノマー,オリゴマー等の低分子量物が混在しているポリ
アミドも用いることが可能である。Further, the polyamide resin that can be used in the present invention is not limited by the type, concentration and molecular weight of the end groups of these polyamides as long as it is selected from the above-mentioned polyamides, and various types can be used. However, high amino unterminated polyamides are especially preferred. It is also possible to use a polyamide in which low molecular weight substances such as monomers and oligomers that remain or are formed during polymerization of the polyamide are mixed.
次に、本発明に用いられる(B)変性ポリオレフィン
としては、各種のものがあるが、通常はカルボン酸基
(酢酸基,アクリル酸基,メタクリル酸基,フマル酸
基,イタコン酸基など),カルボン酸金属塩基(ナトリ
ウム塩,カルシウム塩,マグネシウム塩,亜鉛塩な
ど),カルボン酸エステル基(メチルエステル基,エチ
ルエステル基,プロピルエステル基,ブチルエステル
基,ビニルエステル基など),酸無水物基(無水マレイ
ン酸基など)およびエポキシ基から選ばれた少なくとも
一種の官能基を有するポリオレフィンである。またこの
ポリオレフィンとしては、ポリエチレン,ポリプロピレ
ン,ポリブテン,エチレン/プロピレン共重合体,エチ
レン/ブテン共重合体,エチレン/ヘキセン共重合体さ
らにはこれらに少量のジエンを含む共重合体などをあげ
ることができる。Next, as the (B) modified polyolefin used in the present invention, there are various kinds, but usually, carboxylic acid groups (acetic acid group, acrylic acid group, methacrylic acid group, fumaric acid group, itaconic acid group, etc.), Carboxylic acid metal base (sodium salt, calcium salt, magnesium salt, zinc salt, etc.), carboxylic acid ester group (methyl ester group, ethyl ester group, propyl ester group, butyl ester group, vinyl ester group, etc.), acid anhydride group A polyolefin having at least one functional group selected from (maleic anhydride group and the like) and epoxy group. Examples of the polyolefin include polyethylene, polypropylene, polybutene, ethylene / propylene copolymers, ethylene / butene copolymers, ethylene / hexene copolymers, and copolymers containing a small amount of diene therein. .
このような変性ポリオレフィンの具体例としては、エ
チレン/アクリル酸共重合体,エチレン/メタクリル酸
共重合体,エチレン/フマル酸共重合体,エチレン/メ
タクリル酸/メタクリル酸亜鉛共重合体,エチレン/ア
クリル酸/メタクリル酸ナトリウム共重合体,エチレン
/アクリル酸イソブチル/メタクリル酸/メタクリル酸
亜鉛共重合体,エチレン/メタクリル酸メチル/メタク
リル酸/メタクリル酸マグネシウム共重合体,エチレン
/アクリル酸エチル共重合体,エチレン/酢酸ビニル共
重合体,エチレン/メタクリル酸グリシジル共重合体,
エチレン/酢酸ビニル/メタクリル酸グリシジル共重合
体,無水マレイン酸グラフトポリエチレン,アクリル酸
グラフトポリエチレン,無水マレイン酸グラフトポリプ
ロピレン,無水マレイン酸グラフトエチレン/プロピレ
ン共重合体,アクリル酸グラフトエチレン/プロピレン
共重合体,フマル酸グラフトエチレン/1−ブデン共重合
体,エチレン/1−ヘキセン−イタコン酸共重合体,エチ
レン/プロピレン−エンドビシクロ〔2.2.1〕−5−ヘ
プテン−2,3−無水ジカルボン酸共重合体,エチレン/
プロピレン−メタクリル酸グラフトグリシジル共重合
体,無水マレイン酸グラフトエチレン/プロピレン/1,4
−ヘキサジエン共重合体,フマル酸グラフトエチレン/
プロピレン/ジシクロペンタジエン共重合体,マレイン
酸グラフトエチレン/プロピレン/ノルボルナジエン共
重合体およびアクリル酸グラフトエチレン/酢酸ビニル
共重合体などであり、これらの変性ポリオレフィンを単
独で使用してもよく、また二種以上を併用することも可
能である。Specific examples of such modified polyolefins include ethylene / acrylic acid copolymers, ethylene / methacrylic acid copolymers, ethylene / fumaric acid copolymers, ethylene / methacrylic acid / zinc methacrylate copolymers, ethylene / acrylics. Acid / sodium methacrylate copolymer, ethylene / isobutyl acrylate / methacrylic acid / zinc methacrylate copolymer, ethylene / methyl methacrylate / methacrylic acid / magnesium methacrylate copolymer, ethylene / ethyl acrylate copolymer, Ethylene / vinyl acetate copolymer, ethylene / glycidyl methacrylate copolymer,
Ethylene / vinyl acetate / glycidyl methacrylate copolymer, maleic anhydride grafted polyethylene, acrylic acid grafted polyethylene, maleic anhydride grafted polypropylene, maleic anhydride grafted ethylene / propylene copolymer, acrylic acid grafted ethylene / propylene copolymer, Fumaric acid-grafted ethylene / 1-butene copolymer, ethylene / 1-hexene-itaconic acid copolymer, ethylene / propylene-endobicyclo [2.2.1] -5-heptene-2,3-dicarboxylic anhydride copolymer ,ethylene/
Propylene-methacrylic acid graft glycidyl copolymer, maleic anhydride graft ethylene / propylene / 1,4
-Hexadiene copolymer, fumaric acid graft ethylene /
Propylene / dicyclopentadiene copolymer, maleic acid-grafted ethylene / propylene / norbornadiene copolymer, acrylic acid-grafted ethylene / vinyl acetate copolymer and the like, and these modified polyolefins may be used alone or in combination. It is also possible to use more than one species together.
上記変性ポリオレフィンの製造は公知の方法、例えば
特公昭39−6810号公報,特公昭46−27527号公報,特公
昭50−2630号公報,特公昭52−43677号公報,特公昭53
−5716号公報,特公昭53−19037号公報,特公昭53−411
73号公報,特公昭56−9925号公報などに示された方法に
従って製造することができる。なお、エチレン系アイオ
ノマーについては一般に“サーリン",“ハイミラン",
“コーポレン”なる商品名で市販されている各種グレー
ドを用いることができる。また、本発明で用いられる変
性ポリオレフィンの重合度は特に制限はないが、通常メ
ルトインデックスが0.01〜100g/10分の範囲内にあるも
のを任意に選択できる。The modified polyolefin can be produced by a known method, for example, Japanese Patent Publication No. 39-6810, Japanese Patent Publication No. 46-27527, Japanese Patent Publication No. 50-2630, Japanese Patent Publication No. 52-43677, and Japanese Patent Publication No. 53.
-5716, Japanese Patent Publication No. 53-19037, Japanese Patent Publication No. 53-411
It can be manufactured according to the method described in Japanese Patent Publication No. 73, Japanese Patent Publication No. 56-9925, etc. Regarding ethylene ionomers, "Surlyn", "Himilan",
Various grades marketed under the trade name of "COPOLEN" can be used. Further, the degree of polymerization of the modified polyolefin used in the present invention is not particularly limited, but one having a melt index in the range of 0.01 to 100 g / 10 minutes can be arbitrarily selected.
次に(C)ポリプロピレン樹脂としては、プロピレン
単独重合体および/あるいはプロピレン共重合体が用い
られる。ここでプロピレン共重合体としては、プロピレ
ン−エチレン共重合体,プロピレン−ブテン−1共重合
体などがあり、これらのブロック共重合体やランダム共
重合体が用いられる。なお、このポリプロピレン樹脂
は、プロピレン単独重合体やプロピレン共重合体を一種
類で使用してもよく、あるいは二種類以上併用すること
もできる。この際プロピレン単独重合体,プロピレン共
重合体の分子量は、特に制限されないが、一般にはメル
トフローレート(MFR)が1〜50g/10分のものが好適に
使用される。Next, as the polypropylene resin (C), a propylene homopolymer and / or a propylene copolymer is used. Here, as the propylene copolymer, there are a propylene-ethylene copolymer, a propylene-butene-1 copolymer and the like, and a block copolymer or a random copolymer thereof is used. As the polypropylene resin, one type of propylene homopolymer or propylene copolymer may be used, or two or more types may be used in combination. At this time, the molecular weights of the propylene homopolymer and the propylene copolymer are not particularly limited, but generally, those having a melt flow rate (MFR) of 1 to 50 g / 10 minutes are preferably used.
本発明の組成物では、(A)〜(C)成分として、上
記の如き種々のものが使用可能であるが、これらのうち
(A)成分及び(C)成分の間では、成形加工温度,剪
断速度3500sec-1における(A)成分の溶融粘度ηPA(p
oise)及び(C)成分の溶融粘度ηPP(poise)の比率
が、 式 ηPP/ηPA>0.75 ・・・〔I〕 好ましくは 式 ηPP/ηPA>1 ・・・〔I′〕 を満たすものを組合せて選定することが必要である。こ
こでηPP/ηPAの値が0.75以下であると、得られる樹脂
組成物に所望の塗装性に付与することができず、好まし
くない。なお、ここで成形加工温度とは、本発明の組成
物を成形して各種の成形品を製造する際の温度であり、
一般には180〜350℃の範囲である。In the composition of the present invention, various components as described above can be used as the components (A) to (C). Among them, the molding processing temperature, Melt viscosity of component (A) at a shear rate of 3500 sec -1 η PA (p
oise) and the melt viscosity η PP (poise) of the components (C) have the formula η PP / η PA > 0.75 ... [I], preferably the formula η PP / η PA > 1 ... [I '] It is necessary to select those that meet the requirements. Here, if the value of η PP / η PA is 0.75 or less, it is not preferable because the resin composition obtained cannot be provided with desired coatability. Incidentally, the molding processing temperature here is a temperature at the time of molding various compositions by molding the composition of the present invention,
Generally, it is in the range of 180 to 350 ° C.
本発明において、塗装性に優れたポリアミド・ポリオ
レフィン樹脂組成物を製造するための各成分の配合割合
は、(A)ポリアミド樹脂80〜40重量%(正しくは40重
量%を越え、かつ80重量%以下)、好ましくは80〜45重
量%であり、(B)変性ポリオレフィン1〜40重量%、
好ましくは3〜30重量%である。また、(C)ポリオレ
フィン樹脂は20〜60重量%、好ましくは20〜50重量%で
ある。In the present invention, the blending ratio of each component for producing a polyamide-polyolefin resin composition having excellent coatability is (A) polyamide resin 80 to 40% by weight (correctly exceeding 40% by weight and 80% by weight). The following), preferably 80 to 45% by weight, (B) modified polyolefin 1 to 40% by weight,
It is preferably 3 to 30% by weight. The content of the (C) polyolefin resin is 20 to 60% by weight, preferably 20 to 50% by weight.
ここで、(A)ポリアミド樹脂が40重量%以下では、
得られる組成物の塗装性を充分に改善されない。逆に80
重量%を超えると、ポリプロピレン樹脂本来の特性が失
われる。また、(B)変性ポリオレフィンが1重量%未
満では、(A)成分であるポリアミド樹脂と(C)成分
であるポリプロピレン樹との相溶性を改善することが難
しく、その結果、得られる組成物に所望の物性を付与す
ることができない場合がある。一方、(B)変性ポリオ
レフィンが40重量%を超えても、配合量に相当する効果
は少なく、むしろ得られる樹脂組成物の諸物性を低下さ
せるおそれがある。さらに、(C)ポリプロピレン樹脂
が20重量%未満では、組成物にポリプロピレン本来の特
性を付与することができない。逆に60重量%を超えると
目的とする塗装性の改善効果が充分発現しない。Here, when the (A) polyamide resin is 40% by weight or less,
The coatability of the resulting composition is not sufficiently improved. Conversely 80
When it exceeds the weight percentage, the original properties of the polypropylene resin are lost. Further, if the content of the (B) modified polyolefin is less than 1% by weight, it is difficult to improve the compatibility between the polyamide resin as the component (A) and the polypropylene resin as the component (C), and as a result, the resulting composition is In some cases, it may not be possible to impart desired physical properties. On the other hand, if the content of the modified polyolefin (B) exceeds 40% by weight, the effect corresponding to the blending amount is small, and the various properties of the obtained resin composition may be deteriorated. Further, if the content of the polypropylene resin (C) is less than 20% by weight, it is impossible to impart the original properties of polypropylene to the composition. On the other hand, if it exceeds 60% by weight, the desired effect of improving the paintability is not sufficiently exhibited.
本発明の樹脂組成物は、上記の(A),(B)及び
(C)の三成分を主成分とするものであるが、必要によ
り他の添加剤を上記成分の特性を阻害しない範囲で添加
してもよい。ここで配合できる添加剤としては、染料,
顔料,充填剤,核剤,繊維状物,可塑剤,滑剤,離型
剤,カップリング剤,発泡剤,耐熱剤,耐候剤,難燃
剤,帯電防止剤,摺動剤等が挙げられる。The resin composition of the present invention contains the above-mentioned three components (A), (B) and (C) as the main components, but other additives may be added, if necessary, within a range that does not impair the characteristics of the components. You may add. Additives that can be blended here include dyes,
Examples thereof include pigments, fillers, nucleating agents, fibrous substances, plasticizers, lubricants, release agents, coupling agents, foaming agents, heat-resistant agents, weather-resistant agents, flame retardants, antistatic agents, sliding agents and the like.
本発明の樹脂組成物は、上記三成分及び必要により添
加する添加剤を所定量配合してなる樹脂組成物である。
配合の順序について特に制限はなく、各成分を順次ある
いは同時に配合してもよい。また重合反応終了後の粉末
状あるいはペレット状の(A)成分に(B)及び(C)
成分を配合してもよい。The resin composition of the present invention is a resin composition prepared by blending the above three components and a predetermined amount of an additive to be added if necessary.
The order of compounding is not particularly limited, and the components may be compounded sequentially or simultaneously. Further, the powdery or pelletized component (A) after the completion of the polymerization reaction may be added to the components (B) and (C).
You may mix a component.
本発明の樹脂組成物は、各成分を前述の配合割合で混
合乃至混練することによって調製するが、その方法とし
ては、従来知られている溶融混練法が好ましい。混合は
バンバリーミキサー,ヘンシェルミキサー等を用いて行
われ、混練機としては一般に単軸または二軸の押出機が
用いられる。溶融混練する際の温度は、成分,配合量等
により、各成分の溶融が充分進行しかつ分解しない温度
を適宜選定すればよい。通常は180〜350℃、好ましくは
200〜300℃の範囲で選定される。The resin composition of the present invention is prepared by mixing or kneading the respective components in the above-mentioned mixing ratio, and as a method therefor, a conventionally known melt-kneading method is preferable. Mixing is performed using a Banbury mixer, a Henschel mixer, etc., and as a kneading machine, a single-screw or twin-screw extruder is generally used. The temperature at the time of melt-kneading may be appropriately selected depending on the components, the blending amount, etc., so that the melting of each component does not proceed sufficiently and does not decompose. Usually 180-350 ° C, preferably
It is selected in the range of 200-300 ℃.
得られた樹脂組成物は押出成形,圧縮成形,射出成形
等により任意の形状に成形してパイプ,チューブ等の所
望の樹脂製品とすればよい。さらにその後メッキ,塗装
などの加工を施すこともできる。The obtained resin composition may be molded into an arbitrary shape by extrusion molding, compression molding, injection molding or the like to obtain a desired resin product such as a pipe or a tube. Furthermore, after that, processing such as plating and painting can be performed.
次に、本発明を実施例および比較例に基いてさらに詳
しく説明する。Next, the present invention will be described in more detail based on Examples and Comparative Examples.
なお、以下の各例において得られたポリアミド・ポリ
オレフィン樹脂組成物の各種物性は次の如き試験方法に
基いて測定したものである。The various physical properties of the polyamide / polyolefin resin compositions obtained in the following examples are measured based on the following test methods.
塗装用平板(100×100×3mm厚)の作成法 平板は、組成物をスクリューインライン式射出成形機
で成形した。この時のシリンダー温度は、(A)ポリア
ミド樹脂の種類によらず280℃とした。また、金型温度
は60℃とした。Method for preparing flat plate for coating (100 × 100 × 3 mm thickness) The flat plate was formed by molding the composition with a screw in-line injection molding machine. The cylinder temperature at this time was 280 ° C. regardless of the type of the (A) polyamide resin. The mold temperature was 60 ° C.
溶融粘度 東洋精機(株)製キャピログラフを用い、設定温度28
0℃,剪断速度3500sec-1における溶融粘度を測定した。Melt viscosity Using a Capillograph manufactured by Toyo Seiki Co., Ltd., set temperature 28
The melt viscosity was measured at 0 ° C and a shear rate of 3500 sec -1 .
塗装性 塗料として2液型ポリウレタン樹脂塗料(ストロンエ
ース#680,カシュー(株)製)を用い、平板にスプレー
式で塗布し、乾燥条件は100℃で40分とした。そのサン
プルを1日室温に放置した後、碁盤目剥離試験,塗膜の
密着強度の測定を実施した。Paintability A two-component polyurethane resin paint (Stron Ace # 680, manufactured by Cashew Co., Ltd.) was used as a paint, and spray-applied to a flat plate, and the drying condition was 100 ° C. for 40 minutes. After the sample was left at room temperature for one day, cross-cut peeling test and adhesion strength of the coating film were measured.
実施例1〜9及び比較例1〜4 第1表に示す(A)ポリアミド樹脂,(B)変性ポリ
オレフィン及び(C)ポリプロピレン樹脂を所定量配合
し、ヘンシェルミキサーにより5分間乾式混合を行い、
得られた混合物をベント付同方向二軸押出機(内径30m
m、L/D=17)により溶融混練し、ペレットを作成した。
ペレット作成時の加熱温度もすべて280℃とした。Examples 1 to 9 and Comparative Examples 1 to 4 (A) polyamide resin, (B) modified polyolefin and (C) polypropylene resin shown in Table 1 were blended in predetermined amounts, and dry blended for 5 minutes with a Henschel mixer.
The mixture obtained was ventilated in the same direction twin-screw extruder (inner diameter 30 m
m, L / D = 17) and melt-kneaded to prepare pellets.
The heating temperature at the time of pellet formation was also 280 ° C.
このペレットを減圧下で加熱乾燥した後、射出成形に
より平板を成形し、塗装試験を行った。結果を第1表に
示す。After heating and drying these pellets under reduced pressure, a flat plate was formed by injection molding and a coating test was conducted. The results are shown in Table 1.
なお、この第1表には280℃,剪断速度3500sec-1にお
けるηPP/ηPAを併せて示す。In addition, Table 1 also shows η PP / η PA at 280 ° C. and a shear rate of 3500 sec −1 .
〔発明の効果〕 以上説明したように、本発明のよれば、ポリアミドと
ポリプロピレンのそれぞれの優れた特性を併せ有し、特
に塗装性に優れた各種強化ポリアミド・ポリプロピレン
樹脂組成物を製造することができ、塗装性が要求される
用途に適した樹脂組成物を容易に得ることができる。 [Effects of the Invention] As described above, according to the present invention, it is possible to produce various reinforced polyamide-polypropylene resin compositions having excellent properties of both polyamide and polypropylene, and particularly excellent in coatability. It is possible to easily obtain a resin composition suitable for applications requiring paintability.
従って、本発明のポリアミド・ポリオレフィン樹脂組
成物は、塗装性が要求される自動車部品(外板,外装な
ど),機械部品,工業部品等に好適に利用される。Therefore, the polyamide / polyolefin resin composition of the present invention is suitably used for automobile parts (outer plates, exteriors, etc.), machine parts, industrial parts, etc., which are required to have coatability.
Claims (1)
し、40重量%を除く。),(B)変性ポリオレフィン1
〜40重量%及び(C)ポリプロピレン樹脂20〜60重量%
からなり、かつ成形加工温度,剪断速度3500sec-1にお
ける前記(A)ポリアミド樹脂の溶融粘度ηPA(pois
e)と(C)ポリプロピレン樹脂の溶融粘度ηPP(pois
e)の比が、 式 ηPP/ηPA>0.75 ・・・〔I〕 を満たすことを特徴とするポリアミド・ポリオレフィン
樹脂組成物。1. (A) Polyamide resin 80 to 40% by weight (excluding 40% by weight), (B) Modified polyolefin 1
~ 40 wt% and (C) Polypropylene resin 20-60 wt%
And the melt viscosity η PA (pois of the above-mentioned (A) polyamide resin at a molding processing temperature and a shear rate of 3500 sec −1 .
e) and (C) Polypropylene resin melt viscosity η PP (pois
A polyamide / polyolefin resin composition characterized in that the ratio of e) satisfies the formula η PP / η PA > 0.75 ... [I].
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28478589A JP2695492B2 (en) | 1989-11-02 | 1989-11-02 | Polyamide / polyolefin resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28478589A JP2695492B2 (en) | 1989-11-02 | 1989-11-02 | Polyamide / polyolefin resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03146552A JPH03146552A (en) | 1991-06-21 |
JP2695492B2 true JP2695492B2 (en) | 1997-12-24 |
Family
ID=17682988
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28478589A Expired - Fee Related JP2695492B2 (en) | 1989-11-02 | 1989-11-02 | Polyamide / polyolefin resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2695492B2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH06179815A (en) * | 1992-12-15 | 1994-06-28 | Tosoh Corp | Inorganic filler reinforced polypropylene composition |
JPH0753790A (en) * | 1993-08-12 | 1995-02-28 | Tosoh Corp | Resin composition for metal plating |
ES2137341T3 (en) * | 1993-10-12 | 1999-12-16 | Atochem Elf Sa | OBJECT BASED ON A MIXTURE OF POLYAMIDE AND POLYOLEFIN THAT INCLUDES A WELDING LINE. |
DE69511615T2 (en) * | 1994-05-20 | 1999-12-09 | Ube Industries, Ltd. | Polyamide matrix with resin composite material containing dispersed polyolefin grains |
JP2766875B2 (en) | 1995-04-10 | 1998-06-18 | 日本ピラー工業株式会社 | Shaft sealing system device |
JP4983135B2 (en) * | 2005-08-08 | 2012-07-25 | 三菱瓦斯化学株式会社 | Thermoplastic resin composition molded article with excellent barrier properties |
-
1989
- 1989-11-02 JP JP28478589A patent/JP2695492B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH03146552A (en) | 1991-06-21 |
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