JPH0819256B2 - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JPH0819256B2 JPH0819256B2 JP63152123A JP15212388A JPH0819256B2 JP H0819256 B2 JPH0819256 B2 JP H0819256B2 JP 63152123 A JP63152123 A JP 63152123A JP 15212388 A JP15212388 A JP 15212388A JP H0819256 B2 JPH0819256 B2 JP H0819256B2
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- carbon fiber
- weight
- ratio
- graphite powder
- 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.)
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Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は樹脂組成物に関し、さらに詳しくは耐蝕性ポ
ンプ,ジョイント,パイプ類の成形に有用な樹脂組成物
に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a resin composition, and more particularly to a resin composition useful for forming corrosion resistant pumps, joints and pipes.
耐蝕性ポンプ,ジョイント,パイプ類等には、従来、
ステンレス鋼,ニッケル合金(例えばハステロイ),チ
タン合金等が一般的に用いられている。しかし、これら
は素材自体が高価であること、加工し難いこと、さらに
は金属加工では仕上げ表面内の平滑性が悪く、流体抵抗
の圧損が大きく、ポンプ効率が悪い等の欠点があった。
そのため、最近では、プラスチック素材を用いて射出成
形や圧縮成形により加工コストの低減が図られている。
また、プラスチック素材は、表面の平滑性が良いことか
ら、ポンプ効率の向上等の利点を有する。For corrosion resistant pumps, joints, pipes, etc.
Stainless steel, nickel alloy (for example, Hastelloy), titanium alloy, etc. are generally used. However, these materials have drawbacks in that the material itself is expensive, it is difficult to process, and in the metal processing, the smoothness in the finished surface is poor, the pressure loss of fluid resistance is large, and the pump efficiency is poor.
Therefore, recently, the processing cost has been reduced by injection molding or compression molding using a plastic material.
In addition, since the plastic material has a smooth surface, it has advantages such as improved pump efficiency.
しかしながら、プラスチック素材によるものは、高温
下での強度低下が著しく、使用可能温度範囲に制約があ
った。However, those made of plastic materials have a remarkable decrease in strength at high temperatures, which limits the usable temperature range.
そこで、本発明者らは、高温下でも強度低下が起こら
ず、使用温度範囲が広く、耐蝕性,機械的強度,加工
性,平滑性等において優れたプラスチック素材を開発す
べく鋭意研究を重ねた。Therefore, the inventors of the present invention have conducted intensive studies to develop a plastic material that does not exhibit strength reduction even at high temperatures, has a wide operating temperature range, and has excellent corrosion resistance, mechanical strength, workability, smoothness, and the like. .
その結果、ある種の重合体あるいは共重合体に充填材
として特定の黒鉛粉末と特定の炭素繊維とを組み合わせ
て特定量配合することによって、上記の目的を達成でき
ることを見出した。本発明は、かかる知見に基づいて完
成したものである。As a result, they have found that the above object can be achieved by combining a specific graphite powder and a specific carbon fiber as a filler into a certain polymer or copolymer and compounding them in a specific amount. The present invention has been completed based on such findings.
すなわち、本発明は(a)黒鉛化率70%以上、粒度2
μ以下の黒鉛粉末と黒鉛化率70%以上の炭素繊維とから
なる充填材30〜70重量部および(b)ポリプロピレン,
ポリ二フッ化ビニリデン,ポリテトラフルオロエチレン
−フルオロアルコキシ(PFA)およびフッ化エチレン−
プロピレン共重合体から選ばれた少なくとも一種の樹脂
100重量部からなることを特徴とする樹脂組成物を提供
するものである。That is, the present invention includes (a) a graphitization ratio of 70% or more and a particle size of 2
30 to 70 parts by weight of a filler composed of graphite powder of μ or less and carbon fiber having a graphitization ratio of 70% or more, and (b) polypropylene,
Polyvinylidene difluoride, polytetrafluoroethylene-fluoroalkoxy (PFA) and fluorinated ethylene-
At least one resin selected from propylene copolymers
A resin composition comprising 100 parts by weight is provided.
本発明の樹脂組成物においては、(a)成分である充
填材として特定の黒鉛粉末と特定の炭素繊維とを併用す
る。ここで、黒鉛粉末と炭素繊維をそれぞれ単独で使用
しても得られる樹脂組成物の耐蝕性は向上するが、黒鉛
粉末単独では、強度が不足し、一方、炭素繊維を単独で
使用すると、射出成形時の流れによる配向で、成形品に
ソリねじれが発生し、製品の形状を正確に保持できない
という問題が生ずる。これらの問題を解消するには、上
述の如く黒鉛粉末と炭素繊維とを併用することが必要で
あるが、両者に使用割合については、製造すべき樹脂組
成物(あるいは成形品)の要求特性等により異なり、一
義的に定めることは困難である。しかし、一般には黒鉛
粉末/炭素繊維の重量比を20/80〜80/20、好ましくは30
/70〜60/40の範囲で選定すればよい。In the resin composition of the present invention, a specific graphite powder and a specific carbon fiber are used together as the filler which is the component (a). Here, the corrosion resistance of the resin composition obtained by using the graphite powder and the carbon fiber alone is improved, but the graphite powder alone has insufficient strength, while the carbon fiber alone is used, The orientation due to the flow at the time of molding causes warp twist in the molded product, which causes a problem that the shape of the product cannot be accurately maintained. In order to solve these problems, it is necessary to use graphite powder and carbon fiber together as described above. Regarding the usage ratio of both, the required characteristics of the resin composition (or molded product) to be manufactured, etc. However, it is difficult to set a unique value. However, generally, the weight ratio of graphite powder / carbon fiber is 20 / 80-80 / 20, preferably 30
It may be selected in the range of / 70 to 60/40.
使用する黒鉛粉末は、前記特性を発揮させる上で黒鉛
化率が70%以上であり、且つ粒度がストークス径の測定
法、すなわちアンドレアゼンピペット法で2μ(中心粒
度)以下のものが使用される。The graphite powder used has a graphitization ratio of 70% or more in order to exhibit the above characteristics, and has a particle size of Stokes's measuring method, that is, a particle size of 2 μ (central particle size) or less by the Andreasen pipette method. .
また、炭素繊維は、得られる樹脂組成物の耐薬品性の
要求上、その黒鉛化率は70%以上であることが要求され
るが、ほとんど炭素元素から構成されている繊維状材料
であって、単結晶を生長させて得られる炭素繊維を包含
する。このような繊維としては気相熱分解法による黒鉛
繊維が例示される。なお、繊維の長さは3〜30mm、好ま
しくは6〜25mmである。The carbon fiber is required to have a graphitization ratio of 70% or more due to the requirement for chemical resistance of the obtained resin composition, but it is a fibrous material composed almost entirely of carbon element. , Carbon fibers obtained by growing single crystals. Examples of such fibers include graphite fibers produced by a vapor phase pyrolysis method. The length of the fiber is 3 to 30 mm, preferably 6 to 25 mm.
一方、本発明の樹脂組成物において、(b)成分とし
て用いる樹脂は、ポリプロピレン,ポリフッ化ビニリデ
ン,ポリテトラフルオロエチレン−フルオロアルコキシ
(PFA)およびフッ化エチレン−プロピレン共重合体の
うちから選ばれた一種あるいは二種以上のものである。
ここでポリプロピレンとしては、アイソタクチック構
造,シンジオタクチック構造あるいはアタクチック構造
のいずれのものでもよいが、耐薬品性の点からホモポリ
マーあるいはエチレン含有率4重量%以下のランダムポ
リマーであるのが好ましく、またその重量平均分子量は
30,000〜80,000程度のものが好ましい。ポリフッ化ビニ
リデンは、その重量平均分子量が70,000〜250,000のも
のが好ましい。またPFAは各種のもがあるが、通常はポ
リテトラフルオロエチレン(テフロン)の側鎖に数%程
度のパーフルオロアルコキシ(例えばパーフルオロプロ
ポキシなど)が結合した構造のもので、その重量平均分
子量は70,000〜250,000のものが好ましい。さらにフッ
化エチレン−プロピレン共重合体についても、同程度の
重量平均分子量のもが好ましく、エチレン−プロピレン
共重合体中のフッ化率は20〜42%程度のものが好まし
い。On the other hand, in the resin composition of the present invention, the resin used as the component (b) is selected from polypropylene, polyvinylidene fluoride, polytetrafluoroethylene-fluoroalkoxy (PFA) and fluorinated ethylene-propylene copolymer. One or more than one.
The polypropylene may have an isotactic structure, a syndiotactic structure, or an atactic structure, but is preferably a homopolymer or a random polymer having an ethylene content of 4% by weight or less from the viewpoint of chemical resistance. , And its weight average molecular weight is
It is preferably about 30,000 to 80,000. The polyvinylidene fluoride preferably has a weight average molecular weight of 70,000 to 250,000. There are various types of PFA, but normally, it has a structure in which several percent of perfluoroalkoxy (eg, perfluoropropoxy) is bonded to the side chain of polytetrafluoroethylene (Teflon), and its weight average molecular weight is Those of 70,000 to 250,000 are preferable. Further, the fluorinated ethylene-propylene copolymer preferably has the same weight average molecular weight, and the fluorination ratio in the ethylene-propylene copolymer is preferably about 20 to 42%.
本発明の樹脂組成物において、(a)成分と(b)成
分の配合割合は、本願発明の目的達成上、(b)成分で
ある樹脂100重量部に対して、(a)成分である黒鉛粉
末と炭素繊維との合計が30〜70重量部の範囲から選ばれ
る。In the resin composition of the present invention, the blending ratio of the component (a) and the component (b) is, in order to achieve the object of the present invention, 100 parts by weight of the resin which is the component (b) and the graphite which is the component (a). The total amount of powder and carbon fiber is selected from the range of 30 to 70 parts by weight.
本発明の樹脂組成物は、上記(a)成分,(b)成分
を主成分とするもであるが、必要に応じて一般に高分子
加工分野で用いられている各種の添加剤を適宜配合する
ことができる。添加剤の例としては、金属を含む無機物
質や高分子の接着性を向上させるための各種カップリン
グ剤、例えばシランカップリング剤,滑剤,可塑剤,着
色剤,酸化防止剤,紫外線吸収剤,核剤,安定剤等があ
げられる。The resin composition of the present invention has the above-mentioned components (a) and (b) as the main components, but if necessary, various additives generally used in the field of polymer processing are appropriately mixed. be able to. Examples of additives include various coupling agents for improving the adhesiveness of metal-containing inorganic substances and polymers, such as silane coupling agents, lubricants, plasticizers, colorants, antioxidants, UV absorbers, Examples include nucleating agents and stabilizers.
上記のような(a)成分,(b)成分および不要に応
じて用いられる各種の添加剤の混合は、通常用いられる
混合機、例えばヘンシェルミキサー,ダンプラー,リボ
ンブレンダー等で行われる。混練機としては、一般に単
軸または2軸の押出機が用いられ、このような押出機に
より、通常はまず上記本発明の組成物からなるペレット
が製造され、このペレットを、圧縮成形,射出成形,押
出成形スタンピング成形等により任意の形状に成形して
所望の樹脂製品とすればよい。The components (a) and (b) as described above and various additives that are optionally used are mixed with a commonly used mixer such as a Henschel mixer, a dumpler, and a ribbon blender. As the kneading machine, a single-screw or twin-screw extruder is generally used. With such an extruder, first, pellets made of the composition of the present invention are first produced, and the pellets are compression-molded or injection-molded. The desired resin product may be formed by molding into an arbitrary shape by extrusion molding stamping molding or the like.
次に、実施例および比較例により本発明をさらに詳し
く説明する。なお、実施例及び比較例において使用した
粒状黒鉛の黒鉛化率は70%以上、粒度は2μ以下、炭素
繊維の黒鉛化率は70%以上のものである。Next, the present invention will be described in more detail with reference to Examples and Comparative Examples. The granular graphite used in Examples and Comparative Examples had a graphitization ratio of 70% or more, a particle size of 2 μm or less, and a carbon fiber graphitization ratio of 70% or more.
実施例1 粒状黒鉛5kgと炭素繊維(チョップトストランド,平
均長:13mm)5kgとホモポリプロピレン(MFR=40g/10
分)28.5kgをスクリュー径が40mmでシリンダー長(L)
とスクリュー径(D)の比がL/D=28の二軸押出機を用
い、押出温度200℃で押出し、ペレット化した。Example 1 5 kg of granular graphite, 5 kg of carbon fiber (chopped strand, average length: 13 mm) and homopolypropylene (MFR = 40 g / 10
Min) 28.5kg with screw diameter 40mm and cylinder length (L)
And a screw diameter (D) ratio of L / D = 28 was used to extrude at a temperature of 200 ° C. for pelletization.
次に、130×130mm、厚さ2.0mmの平板の形状でフィル
ムゲートを有する金型で射出成形を行った。Next, injection molding was performed with a die having a film gate in the shape of a flat plate of 130 × 130 mm and a thickness of 2.0 mm.
射出性でのソリを、M/Tの比率(M:射出方向の収縮率,
T;射出方向に対して直角方向の収縮率)を評価手段とし
て上記の成形板について測定したところ、M/T≒1.08
と、流れ異方性の低いことが判明した。The warpage in the injection property, the ratio of M / T (M: shrinkage in the injection direction,
(T; shrinkage ratio in the direction perpendicular to the injection direction) was measured for the above-mentioned molded plate as an evaluation means, and M / T ≈ 1.08
It was found that the flow anisotropy was low.
また、得られた平板を10%硝酸溶液に80℃で100時間
浸漬した後、その引張強度の保持率を比較したところ80
%であった。これと同様の条件で重クロム酸硫酸混液30
%水溶液を用いて測定すると、88%の保持率が認めら
れ、高い耐薬品性が認められた。After immersing the obtained flat plate in a 10% nitric acid solution at 80 ° C for 100 hours, the tensile strength retention ratios were compared.
%Met. Dichlorosulfuric acid / sulfuric acid mixture 30
% Aqueous solution, a retention rate of 88% was observed and high chemical resistance was observed.
一方、ポンプ部品等として使用が想定される90℃での
曲げ強度は350kg/cm2、曲げ弾性率は35000kg/cm2であ
り、高温でも高い強度を保持するこが判明した。On the other hand, the flexural strength at 90 ° C, which is expected to be used as a pump component, is 350 kg / cm 2 , and the flexural modulus is 35000 kg / cm 2 , which proves that it retains high strength even at high temperatures.
実施例2〜5 粒状黒鉛と炭素繊維の重量比(粒状黒鉛/炭素繊維)
をそれぞれ80/20,70/30,30/70,20/80とし、粒状黒鉛と
炭素繊維の総量を全体の35重量%としたこと以外は、実
施例1と同様にして平板を成形し、各種測定を行った。Examples 2-5 Weight ratio of granular graphite and carbon fiber (granular graphite / carbon fiber)
80/20, 70/30, 30/70, 20/80, respectively, and except that the total amount of the granular graphite and the carbon fibers was 35% by weight, a flat plate was formed in the same manner as in Example 1, Various measurements were performed.
その結果、射出成形の収縮比M/Tは、第1表に示すよ
うに1.2以下であり、ソリやねじれは少ないことがわか
った。As a result, it was found that the shrinkage ratio M / T of the injection molding was 1.2 or less as shown in Table 1, and warpage and twist were small.
また、耐薬品性試験は80%以上の保持率を示し、耐薬
品性が良好であることが判明した。Further, the chemical resistance test showed a retention rate of 80% or more, and it was proved that the chemical resistance was good.
比較例1 実施例1において炭素繊維を用いずに、粒状黒鉛とポ
リプロピレンを用い、以下実施例1と同様にして平板を
形成し、各種測定を行った。Comparative Example 1 A flat plate was formed in the same manner as in Example 1 using granular graphite and polypropylene without using carbon fiber in Example 1, and various measurements were performed.
その結果、射出成形の収縮比M/Tは、1.08であった
が、90℃の曲げ強度は目標の300kg/cm2に達しておら
ず、また、90℃の曲げ弾性率も目標の30000kg/cm2に達
しておらず、高温下におけるポンプ部品の使用には不適
当であった。As a result, the injection molding shrinkage ratio M / T was 1.08, but the bending strength at 90 ° C did not reach the target of 300 kg / cm 2, and the bending elastic modulus at 90 ° C was at the target of 30000 kg / Since it did not reach cm 2 , it was unsuitable for the use of pump parts at high temperature.
比較例2 実施例1において、炭素繊維のみをホモポリプロピレ
ン中に35重量%になるように配合し、以下実施例1と同
様にして平板を成形し、各種測定を行った。Comparative Example 2 In Example 1, only carbon fiber was blended in homopolypropylene so as to be 35% by weight, and a flat plate was molded in the same manner as in Example 1 and various measurements were performed.
その結果、射出成形の収縮率M/Tは2.5であり、また15
0×150×150の箱型形状で改めて射出成形をしてみる
と、箱はねじれて型抜きができなかった。As a result, the injection molding shrinkage ratio M / T was 2.5, and
When I tried injection molding again with a box shape of 0x150x150, the box was twisted and could not be die-cut.
上記の実施例および比較例において用いた充填材の組
成および得られた成形品の性質を下記の第1表に示す。The compositions of the fillers used in the above Examples and Comparative Examples and the properties of the molded articles obtained are shown in Table 1 below.
なお、M/Tは130×130×2mmのフィルムゲートの平板金
型で成形したとき収縮比であり、耐薬品性テストAは、
10%硝酸に80℃で100時間浸漬した後の引張強度の保持
率、耐薬品性テストBは、重クロム酸硫酸混液にAと同
じ条件で浸漬した後の引張強度の保持率である。In addition, M / T is the shrinkage ratio when molded with a flat plate mold of 130 × 130 × 2 mm film gate, and the chemical resistance test A is
The retention rate of tensile strength after immersion in 10% nitric acid at 80 ° C. for 100 hours, and the chemical resistance test B is the retention rate of tensile strength after immersion in a mixed solution of dichromic acid and sulfuric acid under the same conditions as A.
〔発明の効果〕 本発明により特定の黒鉛粉末と特定の炭素繊維を充填
材として特定量用いた樹脂組成物によれば、高温での強
度低下が起こらず、射出成形やスタンピング成形におい
てソリ,ヒケ,ねじれ等を発生せず、寸法安定性にすぐ
れ、また耐薬品性にすぐれた成形品を製造することがで
きる。 [Effects of the Invention] According to the resin composition of the present invention, in which a specific amount of a specific graphite powder and a specific amount of carbon fiber are used as a filler, the strength does not decrease at high temperature, and warpage and sink marks are caused in injection molding and stamping molding. A molded product with excellent dimensional stability and chemical resistance without twisting can be manufactured.
したがって、本発明の樹脂組成物は、耐蝕性ポンプ、
ジョイント,パイプ等の成形素材として有効に利用する
ことができる。Therefore, the resin composition of the present invention is a corrosion resistant pump,
It can be effectively used as a molding material for joints and pipes.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08L 27/12 (72)発明者 浜添 修 神奈川県川崎市川崎区千鳥町3―2 昭和 電工株式会社川崎樹脂研究所内 (72)発明者 児玉 明徳 神奈川県川崎市川崎区千鳥町3―2 昭和 電工株式会社川崎樹脂研究所内 (56)参考文献 特開 昭63−12663(JP,A) 特開 昭60−144364(JP,A)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display location C08L 27/12 (72) Inventor Osamu Hamazoe 3-2 Chidori-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa Showa Denko Kawasaki Plastics Research Co., Ltd. (72) Inventor Akinori Kodama 3-2 Chidoricho, Kawasaki-ku, Kawasaki-shi, Kanagawa Showa Denko Co., Ltd. Kawasaki Plastics Research Co., Ltd. (56) Reference JP-A 63-12663 (JP, A) JP Sho 60-144364 (JP, A)
Claims (1)
黒鉛粉末と黒鉛化率70%以上の炭素繊維とからなる充填
材30〜70重量部および(b)ポリプロピレン,ポリ二フ
ッ化ビニリデン,ポリテトラフルオロエチレン−フルオ
ロアルコキシおよびフッ化エチレン−プロピレン共重合
体から選ばれた少なくとも一種の樹脂100重量部とから
なることを特徴とする樹脂組成物。1. A filler 30 to 70 parts by weight comprising (a) a graphite powder having a graphitization ratio of 70% or more and a particle size of 2 μ or less and a carbon fiber having a graphitization ratio of 70% or more, and (b) a polypropylene or a polyfluorine. A resin composition comprising 100 parts by weight of at least one resin selected from vinylidene chloride, polytetrafluoroethylene-fluoroalkoxy and a fluorinated ethylene-propylene copolymer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63152123A JPH0819256B2 (en) | 1988-06-22 | 1988-06-22 | Resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63152123A JPH0819256B2 (en) | 1988-06-22 | 1988-06-22 | Resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01319549A JPH01319549A (en) | 1989-12-25 |
| JPH0819256B2 true JPH0819256B2 (en) | 1996-02-28 |
Family
ID=15533564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63152123A Expired - Lifetime JPH0819256B2 (en) | 1988-06-22 | 1988-06-22 | Resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0819256B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005281466A (en) * | 2004-03-29 | 2005-10-13 | Idemitsu Kosan Co Ltd | Carbon fiber-containing fiber reinforced resin composition with less warping deformation and molded body thereof |
| JP4898179B2 (en) * | 2005-10-07 | 2012-03-14 | 株式会社プライムポリマー | Resin composition for intake system parts of internal combustion engine and intake system parts |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60144364A (en) * | 1984-01-06 | 1985-07-30 | Sumitomo Bakelite Co Ltd | Thermosetting resin composition |
| JPS6312663A (en) * | 1986-07-03 | 1988-01-20 | Tokyo Ink Kk | Colorable electrically conductive resin composition |
-
1988
- 1988-06-22 JP JP63152123A patent/JPH0819256B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01319549A (en) | 1989-12-25 |
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