JPS5980447A - Carbon-fiber reinforced thermoplastic resin composition - Google Patents
Carbon-fiber reinforced thermoplastic resin compositionInfo
- Publication number
- JPS5980447A JPS5980447A JP19006882A JP19006882A JPS5980447A JP S5980447 A JPS5980447 A JP S5980447A JP 19006882 A JP19006882 A JP 19006882A JP 19006882 A JP19006882 A JP 19006882A JP S5980447 A JPS5980447 A JP S5980447A
- Authority
- JP
- Japan
- Prior art keywords
- thermoplastic resin
- resin
- carbon fibers
- reinforced thermoplastic
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は炭素繊維含有複合材料において、炭素繊維、マ
) IJフックス樹脂間接着性を向上させ、優れた機械
的性質を持たせることを特徴とする、表面処理を行なっ
た炭素繊維を配合してなる炭素繊維強化熱可塑性樹脂組
成物に関するものである。[Detailed Description of the Invention] The present invention provides a carbon fiber-containing composite material that is surface-treated to improve adhesion between carbon fibers and IJ Fuchs resins and to provide excellent mechanical properties. The present invention relates to a carbon fiber-reinforced thermoplastic resin composition containing carbon fibers.
これまで、炭素繊維の表面処理は種々検討されている。Until now, various surface treatments of carbon fibers have been studied.
しかしほとんどは熱硬化性樹脂用に関するものが多く実
用的にはエポキシ樹脂を表面処理したものがほとんどで
ある。熱可塑性樹脂をマ) IJソクスとする際の炭素
繊維用表面処理剤の検討は中れまでほとんど検討されて
おらず、炭素繊維の集束剤としてポリアミド、ポリスル
ホン、ポリビニルアルコール等が検討されているにすぎ
ず、これらの重合体炭素繊維に被覆しても充分な界面効
果は得られない。しかも他フィラ含有複合材料と同様に
、炭素繊維強化熱可塑性樹脂(以下CFRTPと略す)
においても、炭素繊維とマトリックス樹脂である各種熱
可塑性樹脂との接着性は複合効果の発現上極めて重要な
因子となる。そこで、本発明者等は、前者の炭素繊維の
集束と炭素繊維、熱可塑性樹脂間の接着性向」二の2つ
の目的を兼ね備えた表面処理剤を見出すべく鋭意検討し
た結果、As樹脂で炭素繊維の表面被覆することにより
チョツプドストランド製造時及び熱可塑性樹脂との複合
時の作業性に優れ、又複合材料としての機械的性質が著
しるしく向上することを見出し、本発明を完成した。However, most of them are for thermosetting resins, and in practical use, most of them are surface-treated epoxy resins. Surface treatment agents for carbon fibers when making IJ socks from thermoplastic resins have hardly been studied, and polyamides, polysulfones, polyvinyl alcohols, etc. have been considered as sizing agents for carbon fibers. Therefore, even if these polymer carbon fibers are coated, a sufficient interfacial effect cannot be obtained. Moreover, like other filler-containing composite materials, carbon fiber reinforced thermoplastic resin (hereinafter abbreviated as CFRTP)
Also, the adhesion between carbon fibers and various thermoplastic resins as matrix resins is an extremely important factor in achieving the composite effect. Therefore, the present inventors conducted extensive research to find a surface treatment agent that has the former two purposes of convergence of carbon fibers and adhesion between carbon fibers and thermoplastic resin. The present invention has been completed based on the discovery that by coating the surface of the composite material, the workability during the production of chopped strands and when composited with a thermoplastic resin is excellent, and the mechanical properties as a composite material are significantly improved.
本発明に用いるAs樹脂としては比粘度n5VC(0,
1Xl)MF’、 25℃テ測定)は、0.2〜1.0
’/yなるものが適当で、好ましくは03〜0.7 m
l /9である。粘度が低すぎろと炭素繊維の集束性が
悪く毛羽立ちが多くなり、チョツプドストランド製造時
及び熱可塑性樹脂との複合時の作業性が悪くなる。。S
]/Cが高すぎると各単繊維への表面処理が困難になり
、複合材料中で各単繊維が分散したとき、マトリクス樹
脂との接着性が悪くなる。又、As樹脂の炭素繊維の被
覆量し工、炭素繊維と表面処理剤の総重量の1〜10重
量%が適当で、好ましくば3〜7重量%である。一般に
表面処理剤被覆量が少量でありすぎると、ストランドの
毛羽立ちが多くなり、チョツプドストランド製造時及び
熱可塑性樹脂との複合時の作業性が悪くなる。又、表面
処理剤の被覆量が多量でありすぎると、処理後の炭素繊
維ストランドの巻き取り性が悪くなったり、表面処理剤
が影響して複合材料全体としての物性が劣るようになる
。A、 S樹脂の組成においてはアクリロニトリル°ス
チレン−5:95〜30 : 70 カ適当である。表
面処理の書法は特に限定されないが、好適な具体例とし
ては、表面処理剤を適当な溶剤1例えばメチルエチルケ
トン、塩化メチレンに溶解し、その中に炭素繊維を一定
速度で浸漬通過させ、その後浴剤を蒸発させて乾燥する
方法が挙げられる。炭素繊維への表面処理剤の被覆量は
、この表面処理剤濃度と炭素繊維の通過速度によって調
節される。The As resin used in the present invention has a specific viscosity of n5VC (0,
1Xl) MF', measured at 25°C) is 0.2 to 1.0
'/y is suitable, preferably 03 to 0.7 m
It is l/9. If the viscosity is too low, the carbon fibers will have poor cohesiveness and will become fluffy, resulting in poor workability during chopped strand production and when compounding with thermoplastic resin. . S
]/C is too high, surface treatment of each single fiber becomes difficult, and when each single fiber is dispersed in the composite material, adhesion with the matrix resin becomes poor. Furthermore, the amount of coating of the carbon fibers with the As resin is suitably 1 to 10% by weight, preferably 3 to 7% by weight, based on the total weight of the carbon fibers and surface treatment agent. Generally, if the coating amount of the surface treatment agent is too small, the strands will become more fluffy and the workability during production of chopped strands and when composited with thermoplastic resin will be impaired. Furthermore, if the coating amount of the surface treatment agent is too large, the winding properties of the carbon fiber strand after treatment will be poor, and the physical properties of the composite material as a whole will be deteriorated due to the influence of the surface treatment agent. The appropriate composition of the A and S resins is acrylonitrile styrene 5:95 to 30:70. The method of surface treatment is not particularly limited, but as a preferred example, the surface treatment agent is dissolved in a suitable solvent such as methyl ethyl ketone or methylene chloride, the carbon fiber is immersed in the solution at a constant speed, and then a bath agent is added. An example is a method of drying by evaporation. The amount of the surface treatment agent coated on the carbon fibers is adjusted by the concentration of the surface treatment agent and the passing speed of the carbon fibers.
本発明の樹脂組成物において用いろ熱可塑性樹脂の具体
例としてはナイロン6、ナイロン6゜6、ナイロン6、
12. ABS、 As、 PC,PE、 PAC。Specific examples of the thermoplastic resin used in the resin composition of the present invention include nylon 6, nylon 6°6, nylon 6,
12. ABS, As, PC, PE, PAC.
MMA、 PI)S、ポリスチレン、ハイインパクトポ
リスチレンなどいずれのものでも適用できるが、特に有
効であるのはABS、As、 ポリスチレン。Any material such as MMA, PI)S, polystyrene, or high-impact polystyrene can be used, but ABS, As, and polystyrene are particularly effective.
ハイインパクトポリスチレンを挙げろことができろ。Can you name high impact polystyrene?
本発明で用いる炭素繊維は、As樹脂が被覆されている
ため従来開発されてきた表面処理を施した炭素繊維に比
べ、」二記熱可塑性樹脂との親和性が著るしく改良され
ており、機械的特性の優れた熱可塑性樹脂組成物とする
ことができる。Since the carbon fibers used in the present invention are coated with As resin, their affinity with thermoplastic resins is significantly improved compared to surface-treated carbon fibers developed in the past. A thermoplastic resin composition with excellent mechanical properties can be obtained.
以下実施例により具体的に説明する。This will be explained in detail below using examples.
実施例1
アクリロニトリル スチレン−15: 85の組成比で
、比粘度nSP/c (0,1%DMF、 25℃で測
定)が表1に示されたA、 S樹脂をメチルエチルケト
ンに溶解し、それに炭素繊維を浸漬通過させ表1に示し
た被覆量のA8樹脂を被覆させ、乾燥した後、チョツプ
ドストランドにカットし、表1に示された熱可塑性樹脂
に含有率20wt%で押出機にかけ、ペレットを得た。Example 1 Acrylonitrile styrene-A and S resins having a composition ratio of 15:85 and a specific viscosity nSP/c (measured in 0.1% DMF at 25°C) shown in Table 1 were dissolved in methyl ethyl ketone, and carbon The fibers were immersed and passed through to be coated with A8 resin in the amount shown in Table 1, dried, cut into chopped strands, and extruded into the thermoplastic resin shown in Table 1 at a content of 20 wt%. Obtained pellets.
そのペレットを射出成形し、物性を測定した結果を表1
に示した。実験番号1〜4は本発明のものを、実験番号
5〜10は比較例を示す。Table 1 shows the results of injection molding the pellets and measuring their physical properties.
It was shown to. Experiment numbers 1 to 4 show the results of the present invention, and experiment numbers 5 to 10 show comparative examples.
尚、物i生計価は、引張試験は八STM−]”1163
8゜曲げ試験はA、STM−D 790 、アイゾツト
衝撃試験はASTIVI−D256に準じて実施した。In addition, the living value of the product is 8 STM-] for the tensile test.”1163
The 8° bending test was conducted according to A, STM-D 790, and the Izot impact test was conducted according to ASTIVI-D256.
表1に示したように、As樹脂で表面処理した炭素繊維
を配合したCFRTDは優れた機械的性質を持つことが
わかる。As shown in Table 1, it can be seen that CFRTD containing carbon fibers surface-treated with As resin has excellent mechanical properties.
手続補正書(方式) 昭和58年3月3日 特許庁長官 若 杉 和 夫 殿 1、事件の表示 昭和57年特許願第190068号 2、発明の名称 3 補正をする者 事件との関係 特許出願人 東京都中央区京橋二丁目3番19号 (603)三菱レイヨン株式会社 取締役社長 金 澤 脩 三 4、代理人 東京都港区虎ノ門二丁目8番1号 昭和58年2月22日付発送 6、補正の対象 明細書 7、補正の内容 明細書の浄書(内容に変更なし) 391−Procedural amendment (formality) March 3, 1982 Mr. Kazuo Wakasugi, Commissioner of the Patent Office 1.Display of the incident 1981 Patent Application No. 190068 2. Name of the invention 3 Person making the amendment Relationship to the case Patent applicant 2-3-19 Kyobashi, Chuo-ku, Tokyo (603) Mitsubishi Rayon Co., Ltd. President and Director Osamu Kanazawa 4. Agent 2-8-1 Toranomon, Minato-ku, Tokyo Sent on February 22, 1982 6. Subject of correction Specification 7. Contents of correction Engraving of the statement (no changes to the contents) 391-
Claims (1)
る炭素繊維強化熱可塑性樹脂組成物。 2、AS樹脂として比粘度n81/C(Q、1%DM
F。 25℃で測定)が03〜o7ml/yであるものを用い
ることを特徴とする特許請求の範囲第1項記載の炭素繊
維強化熱可塑性樹脂組成物。 3 AS樹脂の炭素繊維への被覆量が炭素繊維と表面処
理剤の総重量の1〜10重量%であることを特徴とする
特許請求の範囲第1項記載の炭素繊維強化熱可塑性樹脂
組成物。 4、AS樹脂としてアクリロニトリル:スチレン=5:
95〜30ニア0の範囲内の共重合組成のものを用いる
ことを特徴とする特許請求の範囲第1項記載の炭素繊維
強化熱可塑性樹脂組成物。 5 熱可塑性樹脂としてABS樹脂、AS樹脂。 ポリスチレン、ハイインパクトポリスチレンの中から選
ばれた少なくとも一種の樹脂を用いることを特徴とする
特許請求の範囲第1項記載の炭素繊維強化熱可塑性樹脂
組成物。[Claims] A carbon fiber-reinforced thermoplastic resin composition comprising carbon fiber coated with tAs resin and a thermoplastic resin. 2. Specific viscosity n81/C (Q, 1%DM
F. 2. The carbon fiber-reinforced thermoplastic resin composition according to claim 1, wherein the carbon fiber-reinforced thermoplastic resin composition has a carbon fiber content of 03 to 07 ml/y (measured at 25°C). 3. The carbon fiber-reinforced thermoplastic resin composition according to claim 1, wherein the amount of AS resin coated on the carbon fibers is 1 to 10% by weight of the total weight of the carbon fibers and surface treatment agent. . 4. Acrylonitrile: styrene = 5 as AS resin:
2. The carbon fiber-reinforced thermoplastic resin composition according to claim 1, characterized in that the copolymerization composition is within the range of 95 to 30 Nia0. 5 ABS resin and AS resin as thermoplastic resins. The carbon fiber reinforced thermoplastic resin composition according to claim 1, characterized in that at least one resin selected from polystyrene and high impact polystyrene is used.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19006882A JPS5980447A (en) | 1982-10-29 | 1982-10-29 | Carbon-fiber reinforced thermoplastic resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19006882A JPS5980447A (en) | 1982-10-29 | 1982-10-29 | Carbon-fiber reinforced thermoplastic resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5980447A true JPS5980447A (en) | 1984-05-09 |
JPH0342306B2 JPH0342306B2 (en) | 1991-06-26 |
Family
ID=16251814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19006882A Granted JPS5980447A (en) | 1982-10-29 | 1982-10-29 | Carbon-fiber reinforced thermoplastic resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5980447A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103993480A (en) * | 2013-02-18 | 2014-08-20 | 金发科技股份有限公司 | Carbon-fiber-surface modifying emulsion, preparation method thereof, and modified carbon fiber and molding composition prepared from same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6439453A (en) * | 1987-08-04 | 1989-02-09 | Sekisui Chemical Co Ltd | Downspout device |
-
1982
- 1982-10-29 JP JP19006882A patent/JPS5980447A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6439453A (en) * | 1987-08-04 | 1989-02-09 | Sekisui Chemical Co Ltd | Downspout device |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103993480A (en) * | 2013-02-18 | 2014-08-20 | 金发科技股份有限公司 | Carbon-fiber-surface modifying emulsion, preparation method thereof, and modified carbon fiber and molding composition prepared from same |
Also Published As
Publication number | Publication date |
---|---|
JPH0342306B2 (en) | 1991-06-26 |
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