JP4480984B2 - Chair parts made of metallic polyamide resin - Google Patents
Chair parts made of metallic polyamide resin Download PDFInfo
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- JP4480984B2 JP4480984B2 JP2003382930A JP2003382930A JP4480984B2 JP 4480984 B2 JP4480984 B2 JP 4480984B2 JP 2003382930 A JP2003382930 A JP 2003382930A JP 2003382930 A JP2003382930 A JP 2003382930A JP 4480984 B2 JP4480984 B2 JP 4480984B2
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Description
本発明は、椅子部品用メタリック調ポリアミド樹脂組成物に関する。詳細には光沢、機械的強度に優れた椅子脚に好適なメタリック調ポリアミド樹脂組成物に関する。 The present invention relates to a metallic polyamide resin composition for chair parts. Specifically, the present invention relates to a metallic polyamide resin composition suitable for a chair leg excellent in gloss and mechanical strength.
ポリアミド樹脂はその成形性と優れた機械的性質を有することから、特に構造部品、電機部品、自動車部品等に射出成形体の形で利用されている。特にポリアミド66/6及びポリアミド6/66の共重合体及びポリマーブレンドにガラス繊維を添加して強化したものは、成形品の外観を要求される分野では広く用いられている。例えば、オフィス家具の分野で椅子用の樹脂材料として、特に椅子脚の樹脂材料として、機械的強度の観点から、ガラス繊維等の無機補強材を添加した強化ポリアミド系樹脂が好適に用いられている。
近年、特にオフィス家具の椅子分野に於いては、脚のデザインが重要視され、従来のリブ構造を有した複雑な形状の樹脂脚から、リブ構造を有さない厚肉で単純な形状、且つ細身で美麗な形状の樹脂脚が望まれる傾向がある。更に加えて、高級感をだすために、樹脂脚に金属感(メタリック調)を望む市場ニーズも高い。しかしながら、椅子部品に要求される充分な機械的強度を有し、且つ厚肉でも表面が平滑で良好なメタリック調の外観を有するポリアミド樹脂組成物は知られていない。
Polyamide resins are used in the form of injection molded articles, particularly for structural parts, electrical parts, automobile parts, etc., because of their moldability and excellent mechanical properties. In particular, polyamide 66/6 and polyamide 6/66 copolymers and polymer blends reinforced by adding glass fibers are widely used in fields where the appearance of molded products is required. For example, in the field of office furniture, as a resin material for a chair, particularly as a resin material for a chair leg, a reinforced polyamide resin to which an inorganic reinforcing material such as glass fiber is added is suitably used from the viewpoint of mechanical strength. .
In recent years, especially in the field of chairs for office furniture, the design of the legs has been regarded as important. From the complicated resin legs with the conventional rib structure, the thick and simple shape without the rib structure, and There is a tendency to desire a slim and beautiful resin leg. In addition, there is a high market need for a metallic feel (metallic tone) on the resin legs in order to give a high-class feel. However, there is no known polyamide resin composition having sufficient mechanical strength required for chair parts, having a smooth surface even with a thick wall, and having a good metallic appearance.
下記特許文献1には、ポリアミド樹脂とガラス繊維との組成物を造粒して得た粒状体に、ポリアミド樹脂とアルミニウム粉との組成物を造粒して得た粒状体を混合してなるメリック調外観を有する成形品の成形材料が開示されている。該樹脂材料は強度、剛性及び耐熱性に優れたメタリック調外観を有するポリアミド樹脂成形品の製造を可能とすると記載されている。
しかしながら、該樹脂組成物では、樹脂厚みが厚い椅子部品において良好なメタリック調を得ることが出来なかった。
In the following Patent Document 1, a granule obtained by granulating a composition of polyamide resin and glass fiber is mixed with a granule obtained by granulating a composition of polyamide resin and aluminum powder. A molding material for a molded article having a mellic appearance is disclosed. The resin material is described as being capable of producing a polyamide resin molded article having a metallic appearance with excellent strength, rigidity and heat resistance.
However, with the resin composition, a good metallic tone could not be obtained in a chair component having a thick resin.
また、下記特許文献2には、ポリアミド樹脂、ガラス繊維、金属粉、真珠顔料からなり、且つ真珠顔料を金属粉の1.5倍以上配合してなる樹脂組成物が開示されている。該樹脂組成物は明るいメタリック色調を有し、耐熱老化時の色目保持に優れ、各種用途において有用であると記載されているが、該樹脂組成物では椅子用成形材料としては機械的強度が不充分であった。
いずれの特許文献にも、樹脂厚みが厚い椅子部品用いることができ、良好なメタリック調を得ることができるとの記載もない。
一般に成形品の樹脂厚みが5mmを超える肉厚になると、表面が平滑で良好なメタリック調の外観を有する成形品を得るのが困難になり、未だ厚肉で表面外観が良好なメタリック調を有し、且つ機械的強度も満足する椅子部品に好適な強化ポリアミド樹脂組成物について何ら提案されていないのが現状である。
In any of the patent documents, there is no description that a chair component having a large resin thickness can be used and a good metallic tone can be obtained.
In general, when the resin thickness of the molded product exceeds 5 mm, it becomes difficult to obtain a molded product with a smooth surface and a good metallic appearance, and it still has a metallic appearance with a good thickness and surface appearance. However, the present situation is that no reinforced polyamide resin composition suitable for a chair part satisfying mechanical strength has been proposed.
本発明は、表面光沢が良好で、かつ機械的強度にも優れる椅子部品の成形材料に好適に用いられるメタリック調のポリアミド樹脂組成物および該樹脂組成物からなる、5mm以上の肉厚部を有する椅子部品、特に椅子脚を提供することを目的とする。 The present invention comprises a metallic polyamide resin composition suitably used as a molding material for chair parts having a good surface gloss and excellent mechanical strength, and a thick part of 5 mm or more comprising the resin composition. The object is to provide chair parts, in particular chair legs.
本発明者は、厚肉の成形品に於いて表面が平滑なメタリック調の外観を発現し、且つ機械的強度に優れるポリアミド樹脂組成物を得るべく、鋭意検討した結果、溶融状態から結晶化する際の温度(Tc)が特定範囲にあるポリアミド樹脂と無機補強材及び金属粉末を組み合わせた樹脂組成物が有効である事を見出し、この知見に基づいて本発明をなすに至った。
すなわち、本発明は、
[1] (a)溶融状態から結晶化する際の温度(Tc)が、180〜210℃のポリアミド6、ポリアミド66およびポリアミド6/ポリアミド66の共重合体から選ばれる1種以上のポリアミド樹脂32〜84.8重量%、(b)無機補強材15〜65重量%、(c)平均粒径10〜90μmの金属粉末0.2〜3重量%を含有するメタリック調ポリアミド樹脂組成物からなることを特徴とする5mm以上の肉厚部を有する椅子部品。
As a result of intensive investigations to obtain a polyamide resin composition that exhibits a metallic appearance with a smooth surface and excellent mechanical strength in a thick-walled molded article, the inventor crystallizes from a molten state. The present inventors have found that a resin composition in which a polyamide resin having a specific temperature (Tc) within a specific range, an inorganic reinforcing material, and a metal powder are combined is effective, and based on this finding, the present invention has been made.
That is, the present invention
[ 1 ] (a) One or more polyamide resins 32 selected from polyamide 6, polyamide 66 and polyamide 6 / polyamide 66 copolymer having a temperature (Tc) of crystallization from a molten state of 180 to 210 ° C. ~84.8 wt%, consisting of (b) an inorganic reinforcing material 15 to 65% by weight, (c) contains a metal powder 0.2-3% by weight of the average particle diameter 10~90μm cuttlefish Tarik tone polyamide resin composition A chair part having a thick part of 5 mm or more .
[2] (c)平均粒径10〜90μmの金属粉末が、フレーク状のアルミニウム粉末であることを特徴とする[1]に記載の椅子部品、 [2] (c) an average particle metal powder diameter 10~90μm is flaky, characterized in that an aluminum powder [1] the chair article according to,
[3] (a)ポリアミド樹脂の溶融状態から結晶化する際の温度(Tc)が、180〜195℃であることを特徴とする[1]または[2]に記載の椅子部品、
[4] 椅子部品が椅子脚である[1]〜[3]いずれか一項に記載の椅子部品、
である。
[3] (a) the temperature at the time of crystallization from the molten state of the polyamide resin (Tc), characterized in that a 180-195 ° C. [1] or [2] the chair article according to,
[ 4 ] The chair part according to any one of [1] to [3 ], wherein the chair part is a chair leg,
It is.
本発明は、無機補強材を含むポリアミド樹脂であっても、優れたメタリック調を有するポリアミド樹脂組成物を提供するもので、椅子部品、特に椅子脚などの厚肉成形品であっても表面性状に優れ、良好なメタリック調を有する。また、該ポリアミド樹脂組成物を用いた椅子部品は塗装工程が不要であるために、経済的かつリサイクルが可能な環境負荷の少ないという効果も有する。 The present invention provides a polyamide resin composition having an excellent metallic tone even if it is a polyamide resin containing an inorganic reinforcing material. Even if it is a thick molded product such as a chair part, particularly a chair leg, the surface property is provided. It has excellent metallic tone. In addition, since the chair component using the polyamide resin composition does not require a painting process, it has an effect of being economical and having a low environmental load that can be recycled.
以下、本発明を詳細に説明する。
本発明に用いられる(a)ポリアミド樹脂は、結晶性の脂肪族ポリアミド、芳香族ポリアミドであり、好ましくはポリアミド6、ポリアミド66、ポリアミド6T、ポリアミド6Iであるか、またはそれらの中から選ばれる少なくとも二種類以上の共重合体又は、ポリマーブレンドを挙げることができる。これらのポリアミド樹脂のうち、Tcが180〜210℃、更に好ましくは180℃〜195℃のポリアミド樹脂である。
本発明で言うTcとは、示差走査熱量計(DSC)で測定され、20℃/分で300℃まで昇温して、3分間保持した後、100℃まで降温したときの結晶化のピーク温度で定義される。
Hereinafter, the present invention will be described in detail.
The (a) polyamide resin used in the present invention is a crystalline aliphatic polyamide or aromatic polyamide, preferably polyamide 6, polyamide 66, polyamide 6T, polyamide 6I, or at least selected from them. Two or more kinds of copolymers or polymer blends can be mentioned. Among these polyamide resins, a polyamide resin having a Tc of 180 to 210 ° C, more preferably 180 to 195 ° C.
Tc as referred to in the present invention is measured with a differential scanning calorimeter (DSC), is heated to 300 ° C. at 20 ° C./min, held for 3 minutes, and then the peak temperature of crystallization when the temperature is lowered to 100 ° C. Defined by
該Tcが、210℃を超えると、成形品の表面に無機補強材が表れやすくなり、平滑な表面を得るのが困難になる。この現象は、厚肉の成形品(肉厚5mm以上)を成形した際に顕著になり、該Tcの値が非常に重要となる。
成形品の厚みが薄い場合には、溶融樹脂が型内を流動する際の流速が早く、溶融樹脂が型表面に十分押し付けられながら成形されるため、無機補強材が成形品の表面に表れやすくなり、比較的Tcに関係なく表面平滑な成形品が得られやすく、成形品の厚みが厚い場合には、溶融樹脂の流速が遅くなるため、型表面に十分押し付けられる前に溶融樹脂が固化し、無機補強材が成形品の表面に表れやすくなるものと推測している。
When the Tc exceeds 210 ° C., the inorganic reinforcing material tends to appear on the surface of the molded product, and it becomes difficult to obtain a smooth surface. This phenomenon becomes prominent when a thick molded product (thickness of 5 mm or more) is molded, and the value of Tc is very important.
When the thickness of the molded product is small, the flow rate when the molten resin flows through the mold is high, and the molten resin is molded while being sufficiently pressed against the mold surface, so the inorganic reinforcing material tends to appear on the surface of the molded product. Therefore, it is easy to obtain a molded product having a relatively smooth surface regardless of Tc, and when the thickness of the molded product is thick, the flow rate of the molten resin becomes slow, so that the molten resin is solidified before being sufficiently pressed against the mold surface. It is estimated that the inorganic reinforcing material is likely to appear on the surface of the molded product.
また、該Tcが、180℃を下回ると、成形品表面の固化速度が遅くなりすぎ、成形品を突き出す際に成形品の変形が起こり易く、完全に固化するまで待つと成形サイクル時間中の冷却時間が長くなり好ましくない。
本発明に用いられるポリアミド樹脂の分子量は特に規定するものではないが、好ましくは、ぎ酸溶液粘度(JIS K 6933)15〜65、更に好ましくは20〜60である。このぎ酸溶液粘度がこの領域より高過ぎると流動性が悪くなり、成形品の表面光沢性が低下する。また低すぎると成形品が脆くなり、十分な強度を保持することが出来ない。
本発明のポリアミド樹脂組成物に含まれるポリアミド樹脂量は、32〜84.8重量%が必要であり、43〜79.8重量%であることが好ましい。ポリアミド樹脂量量が32〜84.8重量%の範囲であれば、表面光沢性が良好で機械強度の点でも充分な成形品が得られる。
Further, if the Tc is lower than 180 ° C., the solidification speed of the molded product surface becomes too slow, and the molded product is likely to be deformed when the molded product is ejected. Time is unpreferable.
The molecular weight of the polyamide resin used in the present invention is not particularly specified, but is preferably formic acid solution viscosity (JIS K 6933) 15 to 65, more preferably 20 to 60. When this formic acid solution viscosity is too higher than this region, the fluidity is deteriorated and the surface glossiness of the molded product is lowered. If it is too low, the molded product becomes brittle, and sufficient strength cannot be maintained.
The amount of polyamide resin contained in the polyamide resin composition of the present invention is required to be 32 to 84.8% by weight, and preferably 43 to 79.8% by weight. When the amount of the polyamide resin is in the range of 32 to 84.8% by weight, a molded product having good surface gloss and sufficient mechanical strength can be obtained.
本発明に用いられる(b)無機補強材は、一般に使用されるガラス繊維、ガラスフレーク、炭素繊維、金属繊維、タルク、マイカ、未焼成クレー、針状晶のウォラステナイト、酸化亜鉛ウィスカ、不定形の炭カル・シリカ、アパタイト等が使用され、何ら限定を受けるものではないが、機械的強度の観点から、ガラス繊維が好ましく、平均径9〜14μm、アスペクト比21〜56のガラス繊維がより好ましい。
(b)無機補強材の配合量は15〜65重量%であり、好ましくは20〜55重量%である。成形品の強度、剛性、衝撃性の点から(b)無機補強材の配合量は15重量%以上であることが必要であり、一方、(b)無機補強材の配合量が65重量%を上回ると、成形時の流動性が悪くなり、無機補強材が成形品の表面に現れ易くなる事によって光沢性が低下し、良好なメタリック調が得られない。
The inorganic reinforcing material (b) used in the present invention includes generally used glass fiber, glass flake, carbon fiber, metal fiber, talc, mica, unfired clay, acicular wollastonite, zinc oxide whisker, and irregular shape. Although carbon cal-silica, apatite, etc. are used and are not subject to any limitation, glass fiber is preferable from the viewpoint of mechanical strength, and glass fiber having an average diameter of 9 to 14 μm and an aspect ratio of 21 to 56 is more preferable. .
(B) The compounding quantity of an inorganic reinforcement material is 15 to 65 weight%, Preferably it is 20 to 55 weight%. From the viewpoint of the strength, rigidity and impact of the molded product, the blending amount of (b) inorganic reinforcing material needs to be 15% by weight or more, while (b) the blending amount of inorganic reinforcing material is 65% by weight. If it exceeds the upper limit, the fluidity at the time of molding deteriorates, and the inorganic reinforcing material tends to appear on the surface of the molded product, so that the glossiness is lowered and a good metallic tone cannot be obtained.
本発明に用いられる(c)金属粉末としては、例えば、銅粉末、ステンレススチール粉末、モリブデン粉末、アルミニウム粉末等が挙げられ、また金属をメッキ等で表面処理した粉末も用いることができる。中でもメタリック調を出し易いという観点から、フレーク状のアルミニウム粉末が好ましい。メタリック調は金属粉末粒径に大きく依存し、メタリック調の出し易さから、平均粒径が10〜90μmの金属粉末であることが必要であり、好ましくは平均粒径40〜90μmである。平均粒径が10μmを下回ると、メタリック調の中のギラギラ感が損なわれ、90μmを超えるとギラギラ感が強すぎて好ましくない。
金属粉末の配合量は0.2〜3重量%であり、好ましくは0.2〜2重量%、より好ましくは0.2〜0.8重量%である。この範囲を下回ると、良好なメタリック調が得られず、一方この範囲を上回ると成形品の強度、衝撃性などが損なわれる。
Examples of the (c) metal powder used in the present invention include copper powder, stainless steel powder, molybdenum powder, aluminum powder, and the like, and powder obtained by surface-treating metal with plating or the like can also be used. Of these, flaky aluminum powder is preferred from the viewpoint of facilitating metallic tone. The metallic tone greatly depends on the particle size of the metal powder, and it is necessary that the metal particle has an average particle size of 10 to 90 μm, and the average particle size is preferably 40 to 90 μm, from the viewpoint of easy metallic tone. When the average particle size is less than 10 μm, the glittering feeling in metallic tone is impaired, and when it exceeds 90 μm, the feeling of glare is too strong, which is not preferable.
The compounding amount of the metal powder is 0.2 to 3% by weight, preferably 0.2 to 2% by weight, and more preferably 0.2 to 0.8% by weight. Below this range, good metallic tone cannot be obtained, while above this range, the strength, impact properties, etc. of the molded product are impaired.
また、本発明のメタリック調ポリアミド樹脂組成物を用いて得られた成形品の表面の光沢度、即ち60度グロス(光沢度)の値は、好ましくは60以上、より好ましくは70以上である。本発明において、60度グロスの測定は、FE−120射出成形機(日精樹脂工業(株)製)を用いて、金型表面温度80℃、樹脂温度280℃、保圧力400kgf/cm2、スクリュー前進速度100mm/秒、ゲートサイズ高さ3mm×幅6mmのサイドゲートにて成形した縦120mm×横80mm×厚さ10mmの平板を用い、該平板の表面積φ45mmをJIS Z8741に規定される60°鏡面光沢度測定法で測定した。
本発明のポリアミド樹脂組成物は、その目的を損なわない範囲において、熱安定剤、耐候剤、酸化防止剤、難燃剤、滑剤、離型剤、核剤、無機顔料、染料、エラストマー等を添加する事も可能である。
Moreover, the glossiness of the surface of the molded article obtained by using the metallic polyamide resin composition of the present invention, that is, the value of 60 degree gloss (glossiness) is preferably 60 or more, more preferably 70 or more. In the present invention, 60 degree gloss is measured using an FE-120 injection molding machine (manufactured by Nissei Plastic Industry Co., Ltd.), a mold surface temperature of 80 ° C., a resin temperature of 280 ° C., a holding pressure of 400 kgf / cm 2 , and a screw. Using a flat plate 120mm long x 80mm wide x 10mm thick formed by a side gate with a forward speed of 100mm / second, gate size height 3mm x width 6mm, the surface area φ45mm of the flat plate is 60 ° mirror surface as defined in JIS Z8741 It was measured by a glossiness measurement method.
In the polyamide resin composition of the present invention, a heat stabilizer, a weathering agent, an antioxidant, a flame retardant, a lubricant, a release agent, a nucleating agent, an inorganic pigment, a dye, an elastomer, and the like are added to the extent that the purpose is not impaired. Things are also possible.
本発明のメタリック調ポリアミド樹脂組成物は、構成成分の(a)ポリアミド樹脂と(b)無機補強材を通常の二軸押出機を使って溶融混練し、無機補強材を添加した(A)強化ポリアミド樹脂組成物を得た後、所定量の(c)金属粉末を配合し、押出し機で溶融混練させて得ることも可能であるが、原料となるポリアミド樹脂の一部に所定量の(c)金属粉末を配合し、押出し機で溶融混練させて(B)マスターバッチを得ておき、残りの原料となるポリアミド樹脂と(b)無機補強材を通常の二軸押出機を使って溶融混練し、無機補強材を添加した(A)強化ポリアミド樹脂組成物を得た後、その(A)強化ポリアミド樹脂組成物に上記(B)マスターバッチを添加しドラムブレンダーでブレンドして製造することが無機補強材による金属粉末の損傷を抑えられ、良好なメタリック調を得ることができることから好ましい。原料となるポリアミド樹脂としてポリアミド樹脂混合物を用いる場合は、予めドラムブレンダーを用いてブレンドしておき、そのポリアミド樹脂混合物を使用する。二軸押出機のシリンダー設定温度は290℃で、ポリマーをホッパーから投入した。(b)無機補強材はサイドフィードで入れることが好ましい。ポリマー投入部及び無機補強材投入部は、充分N2でパージしておくことが好ましい。 The metallic polyamide resin composition of the present invention is obtained by melt-kneading the constituent components (a) polyamide resin and (b) inorganic reinforcing material using an ordinary twin screw extruder, and adding the inorganic reinforcing material (A) reinforcement It is possible to obtain a polyamide resin composition, and then mix a predetermined amount of (c) metal powder and melt and knead it with an extruder. ) Metal powder is mixed and melt kneaded in an extruder (B) to obtain a master batch, and the remaining polyamide resin and (b) inorganic reinforcing material are melt kneaded using a normal twin screw extruder. Then, after obtaining the (A) reinforced polyamide resin composition to which the inorganic reinforcing material is added, the (B) master batch is added to the (A) reinforced polyamide resin composition and blended with a drum blender. Metal powder with inorganic reinforcement This is preferable because it can suppress damage and can obtain a good metallic tone. When a polyamide resin mixture is used as a raw material polyamide resin, it is blended in advance using a drum blender, and the polyamide resin mixture is used. The cylinder set temperature of the twin screw extruder was 290 ° C., and the polymer was charged from the hopper. (B) The inorganic reinforcing material is preferably added by side feed. It is preferable that the polymer charging portion and the inorganic reinforcing material charging portion are sufficiently purged with N 2 .
本発明の椅子用部品、椅子脚は、通常の椅子用部品、椅子脚の成形に用いられる射出成形法の他にも中空射出成形法、2色成形法、サンドイッチ成形法、射出圧縮成形法、また捨てキャビティを設けた成形法などが適用でき、何ら限定されるものではない。
本発明のポリアミド樹脂組成物で成形した成形品は、メタリック調外観、光沢性、機械的特性に優れたものであり、厚肉部品の椅子用部品に好適である、該部品の中でもオフィス用椅子の脚に特に好適ある。
The chair parts and chair legs of the present invention are hollow injection molding methods, two-color molding methods, sandwich molding methods, injection compression molding methods, as well as normal chair parts, injection molding methods used for molding chair legs, Further, a molding method or the like provided with a discarded cavity can be applied, and is not limited at all.
The molded article molded with the polyamide resin composition of the present invention is excellent in metallic appearance, gloss, and mechanical properties, and is suitable for thick-walled chair parts. Among these parts, office chairs Particularly suitable for legs.
以下、実施例により本発明を更に詳細に説明する。
(a)ポリアミド樹脂
(a1)ポリアミド6/ポリアミド66=9/1(重量比)の共重合体:ぎ酸溶液粘度35である。アジピン酸とヘキサメチレンジアミンの等モル塩90wt%とε−カプロラクタム10wt%を通常の溶融重合を行って得た。
(a2)ポリアミド6:射出成形用グレード 宇部興産(株)製
(a3)ポリアミド66:商品名 レオナ1300 旭化成(株)製
(b)ガラス繊維
旭ファイバーグラス(株)社製 商品名 CS0 3JA416
(c)金属粉末
東洋アルミニウム(株)社製 商品名 メタックス
Hereinafter, the present invention will be described in more detail with reference to examples.
(A) Polyamide resin (a1) Polyamide 6 / Polyamide 66 = 9/1 (weight ratio) copolymer: Formic acid solution viscosity 35. 90 wt% of equimolar salt of adipic acid and hexamethylenediamine and 10 wt% of ε-caprolactam were obtained by ordinary melt polymerization.
(A2) Polyamide 6: Injection molding grade Ube Industries, Ltd. (a3) Polyamide 66: Trade name Leona 1300, Asahi Kasei Corporation (b) Glass fiber, Asahi Fiber Glass Co., Ltd. Trade name CS0 3JA416
(C) Metal powder manufactured by Toyo Aluminum Co., Ltd.
<ポリアミド樹脂組成物の製造方法>
(a1)、(a2)、(a3)を表中の組成比でドラムブレンダーを用いてブレンドし、ポリアミド樹脂組成物を得た。次いでこれらの樹脂と(b)ガラス繊維を二軸押出機(池貝鉄工社製 PCM45)を使って次の条件で溶融混練した。
二軸押出機のシリンダー設定温度290℃、スクリュー回転数を150rpm、ポリマーをホッパーから投入した。(b)ガラス繊維は、C5(Zone5)から樹脂組成物のガラス繊維含有量が15〜65wt%に成るようにサイドフィードで入れた。ポリマー投入部及びガラス繊維投入部は、充分N2でパージした。またC7(Zone7)からベント真空を行った(300mmHg)。この様にして、無機補強材を添加した(A)強化ポリアミド樹脂組成物を得た。
また、ポリアミド樹脂に20重量%の(c)金属粉末を配合し、押出し機で溶融混練させて(B)マスターバッチを得た。
上記(A)強化ポリアミド樹脂組成物と、(B)マスターバッチを金属粉末が表中の組成になる様に、ドラムブレンダーを用いてブレンドを行い成形用材料を得た。
<Manufacturing method of polyamide resin composition>
(A1), (a2), and (a3) were blended at a composition ratio in the table using a drum blender to obtain a polyamide resin composition. Next, these resins and (b) glass fibers were melt-kneaded under the following conditions using a twin-screw extruder (PCM45 manufactured by Ikekai Tekko Co., Ltd.).
The cylinder set temperature of the twin screw extruder was 290 ° C., the screw rotation speed was 150 rpm, and the polymer was charged from the hopper. (B) The glass fiber was added by side feed so that the glass fiber content of the resin composition was 15 to 65 wt% from C5 (Zone 5). The polymer charging part and the glass fiber charging part were sufficiently purged with N 2 . A vent vacuum was performed from C7 (Zone 7) (300 mmHg). In this way, (A) reinforced polyamide resin composition to which an inorganic reinforcing material was added was obtained.
Further, 20% by weight of (c) metal powder was blended with the polyamide resin and melt-kneaded with an extruder to obtain (B) a master batch.
The molding material was obtained by blending the (A) reinforced polyamide resin composition and the (B) masterbatch using a drum blender so that the metal powder had the composition shown in the table.
また、実施例、比較例中のTc測定、評価は次の方法で行った。
(1)結晶化温度(Tc)の測定
溶融状態から結晶化する際の温度(Tc)は、押出機より得た無機補強材を添加した(A)強化ポリアミド樹脂組成物を、示差走査熱量計(DSC)(Pyris 1 PERKIN ELMER社製)を用いて、20℃/分で300℃まで昇温して、3分間保持した後、100℃まで降温したときのピーク温度を結晶化温度(Tc)とした。
Moreover, Tc measurement and evaluation in Examples and Comparative Examples were performed by the following methods.
(1) Measurement of crystallization temperature (Tc) The temperature (Tc) at the time of crystallization from a molten state was obtained by adding a reinforcing polyamide resin composition obtained by adding an inorganic reinforcing material from an extruder to a differential scanning calorimeter. Using (DSC) (manufactured by Pyris 1 PERKIN ELMER), the temperature was raised to 300 ° C. at 20 ° C./min, held for 3 minutes, and then the peak temperature when the temperature was lowered to 100 ° C. was crystallized temperature (Tc) It was.
(2)成形品表面外観
FE−120射出成形機(日精樹脂工業(株)製)を用いて、金型表面温度80℃、樹脂温度280℃、保圧力400kgf/cm2、スクリュー前進速度100mm/秒、ゲートサイズ高さ3×幅6mmのサイドゲートにて成形した縦120mm×横80mm×厚さ10mmの平板を用い、該平板の表面積φ45mmをJIS K8741に規定される60°鏡面光沢度測定法(デジタル変角光沢計:スガ試験機(株)製)で測定した。
メタリック調の判定は目視で行い、○:良好なメタリック調、×:表面光沢が低い又はメタリック調だが良好ではない(ギラギラ感が不足、ギラギラ感が過剰)、の2段階で評価を実施した。
(2) Molded product surface appearance Using an FE-120 injection molding machine (manufactured by Nissei Plastic Industry Co., Ltd.), the mold surface temperature is 80 ° C., the resin temperature is 280 ° C., the holding pressure is 400 kgf / cm 2 , and the screw advance speed is 100 mm / Second, using a flat plate 120 mm long x 80 mm wide x 10 mm thick formed by a side gate with a gate size of height 3 x width 6 mm, the surface area φ45 mm of the flat plate is a 60 ° specular gloss measurement method specified in JIS K8741 It was measured with a digital variable gloss meter: manufactured by Suga Test Instruments Co., Ltd.
Judgment of the metallic tone was performed visually, and evaluation was performed in two stages: ◯: good metallic tone, ×: low surface gloss or metallic tone but not good (insufficient glare feeling, excessive glare feeling).
(3)引張り強さ
PS−40E5A射出成形機(日精樹脂工業株式会社製)を用いて、金型表面温度80℃、樹脂温度280℃、保圧力400gf/cm2、スクリュー前進速度100mm/secにて、ISO−527に規定される試験片1A形を成形し、成形後ただちにダンベル片をアルミ袋内に入れヒートシールを行い密閉し、更に23℃環境下×48時間放置させて状態調節したその後、引張り速度5mm/minにて評価を実施した。また光沢度、引張り強さは、各5回測定した平均値を示した。
(3) Tensile strength Using a PS-40E5A injection molding machine (manufactured by Nissei Plastic Industry Co., Ltd.), mold surface temperature 80 ° C., resin temperature 280 ° C., holding pressure 400 gf / cm 2 , screw advance speed 100 mm / sec. After forming the test piece 1A type defined in ISO-527, immediately after molding, the dumbbell piece was put in an aluminum bag and sealed by heat sealing. Evaluation was carried out at a pulling speed of 5 mm / min. Moreover, the glossiness and the tensile strength showed the average value measured 5 times each.
(4)冷却時間
(1)成形品表面外観と同じ成形機、金型、成形条件で成形を行った。成形サイクル中の射出時間は20秒として、冷却時間を変更し正常な成形品が得られる最短の冷却時間を得た。正常な成形品とは、離型時に突き出しピンが成形品へのくい込み、突き破りのない成形品を示す。
(4) Cooling time (1) Molding was performed with the same molding machine, mold, and molding conditions as the molded product surface appearance. The injection time during the molding cycle was 20 seconds, and the cooling time was changed to obtain the shortest cooling time for obtaining a normal molded product. A normal molded product refers to a molded product in which the protruding pin bites into the molded product at the time of mold release and does not break through.
[実施例1〜4、比較例1〜2]
表1はポリアミドのマトリックスを構成する組成の影響を示す。表1に示す組成比で得られた成形品を用いて、評価した結果を表1に示す。
外観及び冷却時間を比較する為、(b)ガラス繊維、(c)アルミニウムフレークの配合量、形状は一定とし、(a1)共重合体、(a2)ポリアミド6、(a3)ポリアミド66の組成比を変更した。実施例1〜4は外観が良好なのに加えて、冷却時間が30秒未満なのに比べて、比較例1では外観は良好だが、冷却時間が30秒以上であった。また比較例2はグロスが低かった。
[Examples 1-4, Comparative Examples 1-2]
Table 1 shows the influence of the composition constituting the polyamide matrix. Table 1 shows the results of evaluation using molded products obtained with the composition ratios shown in Table 1.
In order to compare the appearance and cooling time, the blending amount and shape of (b) glass fiber, (c) aluminum flakes are constant, (a1) copolymer, (a2) polyamide 6, (a3) composition ratio of polyamide 66 Changed. In addition to the good appearance of Examples 1 to 4, the cooling time was 30 seconds or longer in Comparative Example 1, although the appearance was good in Comparative Example 1 compared to the cooling time of less than 30 seconds. In Comparative Example 2, the gloss was low.
[実施例5〜6、比較例3〜4]
表2はガラス繊維の配合量による影響を示す。表2に示す組成比で得られた成形品を用いて、評価した結果を表2に示す。
外観及び引張り強さを比較する為、(a1)共重合体、(a2)ポリアミド6、(a3)ポリアミド66の組成比、(c)アルミニウムフレークの配合量、形状は一定とし、(b)ガラス繊維の配合量を変更した。実施例5〜6は外観が良好なのに加えて、引張り強さが100MPa以上なのに比べて、比較例3はガラス繊維が少ないために外観は良好だが、引張り強さが100MPa未満であった。また比較例4はガラス繊維が多いためグロスが低かった。
[Examples 5-6, Comparative Examples 3-4]
Table 2 shows the effect of the glass fiber content. Table 2 shows the results of evaluation using molded products obtained at the composition ratios shown in Table 2.
In order to compare the appearance and tensile strength, the composition ratio of (a1) copolymer, (a2) polyamide 6, (a3) polyamide 66, (c) the blending amount and shape of aluminum flakes are constant, and (b) glass The amount of fiber was changed. In addition to the good appearance of Examples 5 to 6, the tensile strength was less than 100 MPa compared to Comparative Example 3, although the appearance of Comparative Example 3 was good because there were few glass fibers. Moreover, since the comparative example 4 had many glass fibers, the gloss was low.
[実施例7〜8、比較例5〜7]
表3はアルミニウムフレークの配合量による影響を示す。表3に示す組成比で得られた成形品を用いて、評価した結果を表3に示す。
外観及び引張り強さを比較する為、(a1)共重合体、(a2)ポリアミド6、(a3)ポリアミド66の組成比、(b)ガラス繊維の配合量、(c)アルミニウムフレークの粒径を一定とし、(c)アルミニウムフレークの配合量を変更した。実施例7〜8は外観が良好なのに比べて、比較例5〜6はアルミニウムフレークの配合量が少ない、又は多いため、良好なメタリック調ではなかった。
またアルミニウムフレークの配合量が1重量%の実施例1と、比較例7とを比較すると、アルミニウムフレークを1重量%配合しても引張り強さの低下はほとんどなかった。
[Examples 7-8, Comparative Examples 5-7]
Table 3 shows the influence of the amount of aluminum flakes. Table 3 shows the results of evaluation using molded products obtained at the composition ratios shown in Table 3.
In order to compare the appearance and the tensile strength, the composition ratio of (a1) copolymer, (a2) polyamide 6, (a3) polyamide 66, (b) compounding amount of glass fiber, (c) particle size of aluminum flakes (C) The amount of aluminum flake blended was changed. Compared with Examples 7 to 8 having a good appearance, Comparative Examples 5 to 6 were not good metallic tones because the amount of aluminum flakes contained was small or large.
Further, when Example 1 in which the blending amount of aluminum flakes was 1% by weight and Comparative Example 7 were compared, even if aluminum flakes were blended in 1% by weight, there was almost no decrease in tensile strength.
[実施例9〜10、比較例8〜9]
表4はアルミニウムフレークの粒径による影響を示す。表4に示す組成比で得られた成形品を用いて、評価した結果を表4に示す。
外観を比較する為、(a1)共重合体、(a2)ポリアミド6、(a3)ポリアミド66の組成比、(b)ガラス繊維の配合量、(c)アルミニウムフレークの配合量を一定とし、(c)アルミニウムフレークの粒径を変更した。実施例9〜10は外観が良好なのに比べて、比較例8〜9はアルミニウムフレークの粒径が小さい、又は大きいため良好なメタリック調ではなかった。
[Examples 9 to 10, Comparative Examples 8 to 9]
Table 4 shows the effect of aluminum flake particle size. Table 4 shows the results of evaluation using molded products obtained with the composition ratios shown in Table 4.
In order to compare the appearance, the composition ratio of (a1) copolymer, (a2) polyamide 6, (a3) polyamide 66, (b) glass fiber content, (c) aluminum flake content is constant, c) The particle size of the aluminum flakes was changed. Compared with Examples 9-10 having a good appearance, Comparative Examples 8-9 were not good metallic tones because the particle size of the aluminum flakes was small or large.
[実施例11]
表5に示す樹脂組成で、椅子の5本脚(最大厚さ50mm、高さ120mm、最大直径650mm、ゲートサイズ:ディスクゲート厚み3mm)を1000tの射出成形機を用いて、金型温度80℃設定、樹脂温度280℃、射出圧力800kgf/cm2、保圧力400kgf/cm2、スクリュー前進速度100mm/secにて成形した。
ここで得られた成形品を万能試験機(インストロン社製)を用いて、圧縮速度5mm/minで圧縮試験を行った。この時に破壊が起こった圧縮強度は25kNであった。圧縮強度は、3回測定した平均値を示した。評価結果を表5に示す。
この結果から明らかなように、本発明の樹脂組成物で射出成形された椅子の脚は、実用に耐える強度を有する事が分かる。
[Example 11]
Using a resin composition shown in Table 5, five chair legs (maximum thickness 50 mm, height 120 mm, maximum diameter 650 mm, gate size: disk gate thickness 3 mm) using a 1000 t injection molding machine, mold temperature 80 ° C. setting a resin temperature of 280 ° C., injection pressure 800 kgf / cm 2, holding pressure 400 kgf / cm 2, it was molded at a screw forward speed 100 mm / sec.
The molded product obtained here was subjected to a compression test at a compression speed of 5 mm / min using a universal testing machine (manufactured by Instron). The compressive strength at which breakage occurred at this time was 25 kN. The compressive strength showed the average value measured 3 times. The evaluation results are shown in Table 5.
As is clear from this result, it can be seen that the legs of the chair injection-molded with the resin composition of the present invention have a strength that can withstand practical use.
本発明の椅子部品用メタリック調ポリアミド樹脂組成物で成形した椅子部品、その中でも、特に厚肉部品、具体的にはオフィス用椅子の脚は、メタリック調外観、光沢性、機械的特性に優れたものであり、オフィス用、住宅用部品として好適である。 Chair parts molded with the metallic polyamide resin composition for chair parts of the present invention, among them, particularly thick parts, specifically, office chair legs, have excellent metallic appearance, gloss, and mechanical properties. It is suitable for office and residential parts.
Claims (4)
であることを特徴とする請求項1または2に記載の椅子部品。 (A) The temperature (Tc) for crystallization from the molten state of the polyamide resin is 180 to 195 ° C.
Seat part article according to claim 1 or 2, characterized in that.
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| JPH04236235A (en) * | 1991-01-17 | 1992-08-25 | Showa Denko Kk | Leg for business device or the like |
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