JPH0267326A - Fiber-reinforced thermoplastic resin composition with excellent surface flatness - Google Patents
Fiber-reinforced thermoplastic resin composition with excellent surface flatnessInfo
- Publication number
- JPH0267326A JPH0267326A JP21849588A JP21849588A JPH0267326A JP H0267326 A JPH0267326 A JP H0267326A JP 21849588 A JP21849588 A JP 21849588A JP 21849588 A JP21849588 A JP 21849588A JP H0267326 A JPH0267326 A JP H0267326A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- thermoplastic resin
- filler
- diameter
- 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
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 34
- 239000011342 resin composition Substances 0.000 title claims description 14
- 239000000835 fiber Substances 0.000 claims abstract description 30
- 239000000945 filler Substances 0.000 claims abstract description 25
- 239000012783 reinforcing fiber Substances 0.000 claims abstract description 24
- 239000000203 mixture Substances 0.000 claims description 24
- 239000003365 glass fiber Substances 0.000 abstract description 10
- 239000004927 clay Substances 0.000 abstract description 6
- -1 polyethylene Polymers 0.000 description 24
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 239000004743 Polypropylene Substances 0.000 description 11
- 229920001155 polypropylene Polymers 0.000 description 11
- 239000000843 powder Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001955 polyphenylene ether Polymers 0.000 description 4
- 235000012239 silicon dioxide Nutrition 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 230000003014 reinforcing effect Effects 0.000 description 3
- 229910052580 B4C Inorganic materials 0.000 description 2
- 229910052582 BN Inorganic materials 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000004760 aramid Substances 0.000 description 2
- 229910052790 beryllium Inorganic materials 0.000 description 2
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- PQHRHABVSWOYPG-UHFFFAOYSA-N 2,9-dioxatricyclo[8.2.2.24,7]hexadeca-1(13),4,6,10(14),11,15-hexaene-3,8-dione Chemical compound O1C(=O)C(C=C2)=CC=C2C(=O)OC2=CC=C1C=C2 PQHRHABVSWOYPG-UHFFFAOYSA-N 0.000 description 1
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 1
- YCGKJPVUGMBDDS-UHFFFAOYSA-N 3-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2C=3C=C2C=CC=3)=C1 YCGKJPVUGMBDDS-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920001410 Microfiber Polymers 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 1
- 229920001893 acrylonitrile styrene Polymers 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、繊維補強熱可塑性樹脂組成物に関するもので
あり、更に詳しくは、機械的物性とシートの表面平滑性
に優れた繊維補強熱可塑性樹脂組成物に関するものであ
る。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a fiber-reinforced thermoplastic resin composition, and more specifically, a fiber-reinforced thermoplastic resin composition that has excellent mechanical properties and sheet surface smoothness. This invention relates to a resin composition.
熱可塑性樹脂と補強繊維とからなる繊維補強熱可塑性樹
脂組成物としては、チョツプドガラス繊維をマトリック
ス樹脂に分散させたFRTP、あるいはガラスの長繊維
からなるスワールマットを補強層とする繊維補強熱可望
性樹脂シートが良く知られている。Examples of fiber-reinforced thermoplastic resin compositions consisting of a thermoplastic resin and reinforcing fibers include FRTP in which chopped glass fibers are dispersed in a matrix resin, or fiber-reinforced thermoplastic resin compositions in which a swirl mat made of long glass fibers is used as a reinforcing layer. Resin sheets are well known.
しかしながら、これらの繊維補強熱可塑性樹脂組成物お
よびシートはガラス繊維を用いていることから、成形品
の表面平滑性は悪い。特に、スワールマットを補強繊維
とするときは、成形時に溶融樹脂中表面から繊維が突き
出るため表面平滑性は極めて悪い。このスワールマット
を使用する欠点を克服するものとして、特開昭60−1
58228号公報に開示されている「高い弾性率を有し
、かつ大部分が7mmから50mmの長さと13μm以
下の直径を有する2Of!璽%から60重量%の補強繊
維と40重量%から80重景%の熱可塑性物質とからな
る繊維補強シート」があるが、表面平滑性は今一つ不足
で満足できるものではない。However, since these fiber-reinforced thermoplastic resin compositions and sheets use glass fibers, the surface smoothness of the molded products is poor. In particular, when swirl mats are used as reinforcing fibers, the fibers protrude from the surface of the molten resin during molding, resulting in extremely poor surface smoothness. To overcome the disadvantages of using this swirl mat, JP-A-60-1
No. 58228 discloses that "2Of! reinforcing fibers having a high elastic modulus and mostly having a length of 7 mm to 50 mm and a diameter of 13 μm or less and 40% to 80% of reinforcing fibers by weight. There is a fiber-reinforced sheet made of a thermoplastic material of approximately 50%, but the surface smoothness is not satisfactory.
本発明者等は、このような事情に鑑み、鋭意検討した結
果、マトリックス樹脂に特定の充填剤を添加することに
よって成形品表面の平滑性に優れた繊維補強熱可塑性樹
脂組成物を提供できることを見出して本発明を完成した
。In view of these circumstances, the present inventors have conducted intensive studies and found that by adding a specific filler to the matrix resin, it is possible to provide a fiber-reinforced thermoplastic resin composition with excellent surface smoothness of molded products. They discovered this and completed the present invention.
すなわち、本発明は、
(A)熱可塑性樹脂40〜80重量%および繊維径3〜
20μm1繊維長1〜50aaの補強繊維60〜20重
量%からなる組成物、99〜50重量%と(B)充填剤
、1〜50重量%とからなり、(C)前記充填剤のアス
ペクト比が3未満のときは、その内挿球の直径が、また
、同アスペクト比が3以上のときはその繊維径が前記補
強繊維径のX以下であり、かつ、(D)前記充填剤と前
記熱可塑性樹脂とのに成分の組成物の線膨張率が前記熱
可塑性樹脂の線膨張率の90%以下となるような組成比
で前記充填剤を含存することを特徴とする表面平滑性に
優れた繊維補強熱可塑性樹脂組成物を提供する。That is, the present invention comprises (A) a thermoplastic resin of 40 to 80% by weight and a fiber diameter of 3 to 80% by weight;
A composition consisting of 60 to 20% by weight of reinforcing fibers of 20 μm/fiber length 1 to 50 aa, 99 to 50% by weight, and (B) a filler, 1 to 50% by weight, and (C) the aspect ratio of the filler is When the aspect ratio is less than 3, the diameter of the interpolated sphere, and when the aspect ratio is 3 or more, the fiber diameter is less than or equal to the reinforcing fiber diameter, and (D) the filler and the heat The filler is contained in a composition ratio such that the coefficient of linear expansion of the component composition with the plastic resin is 90% or less of the coefficient of linear expansion of the thermoplastic resin, and has excellent surface smoothness. A fiber reinforced thermoplastic resin composition is provided.
本発明に用いる熱可塑性樹脂は、ポリエチレン、ポリプ
ロピレン等のポリオレフィン樹脂、ポリスチレン、ゴム
補強ポリスチレン、アクリロニトリル−スチレン共重合
体、ABS樹脂等のスチレン系樹脂、ポリエチレンテレ
フタレート、ポリブチレンテレフタレート等のポリエス
テル樹脂、ナイロン6、ナイロン66、ナイロン46等
のポアミド樹脂、ポリフェニレンエーテル、変性ポリフ
ェニレンエーテル等のポリエーテル系樹脂、ポリオキシ
メチレン系樹脂、ポリカーボネート樹脂、ボリアリレー
ト、ポリフェニレンサルファイド、ポリスルホン、ポリ
エーテルスルホン、ポリエーテルエーテルケトン、ポリ
エーテルイミド等の超耐熱樹またはポリカーボネート/
ABS、ポリフェニレンエーテル/ポリアミド、ポリカ
ーボネート/ポリブチレンテレフタレート、ポリフェニ
レンエーテル/ポリブチレンテレフタレート等のブレン
ドポリマー類が挙げられる。Thermoplastic resins used in the present invention include polyolefin resins such as polyethylene and polypropylene, polystyrene, rubber-reinforced polystyrene, acrylonitrile-styrene copolymers, styrenic resins such as ABS resins, polyester resins such as polyethylene terephthalate and polybutylene terephthalate, and nylon. 6. Poamide resins such as nylon 66 and nylon 46, polyether resins such as polyphenylene ether and modified polyphenylene ether, polyoxymethylene resins, polycarbonate resins, polyarylates, polyphenylene sulfides, polysulfones, polyether sulfones, polyether ether ketones , super heat-resistant wood such as polyetherimide or polycarbonate/
Examples include blend polymers such as ABS, polyphenylene ether/polyamide, polycarbonate/polybutylene terephthalate, and polyphenylene ether/polybutylene terephthalate.
本発明に用いる補強繊維は、本発明に用いる熱可塑性樹
脂の引張り弾性率よりも高い弾性率をもつものであれば
何でも良く、例えば、ガラス繊維、カーボン繊維、セラ
ミックス繊維、鉱物繊維等の無機繊維、ステンレス、黄
銅等の金属繊維、超高分子量ポリエチレン繊維、ポリオ
キシメチレン繊維、ポリビニルアルコール繊維、液晶性
芳香族ポリエステル繊維、ポリエチレンテレフタレート
繊維、ポリ−p−フェニレンテレフタレート繊維、ポリ
−m−フェニレンイソフタルアミド繊維等のアラミド繊
維、ポリフェニレンベンゾチアゾール繊維、ポリアクリ
ロニトリル繊維、セルローズ繊維等の有機繊維等が挙げ
られる。The reinforcing fibers used in the present invention may be of any type as long as they have a tensile modulus higher than the tensile modulus of the thermoplastic resin used in the present invention, such as inorganic fibers such as glass fibers, carbon fibers, ceramic fibers, and mineral fibers. , stainless steel, metal fibers such as brass, ultra-high molecular weight polyethylene fibers, polyoxymethylene fibers, polyvinyl alcohol fibers, liquid crystalline aromatic polyester fibers, polyethylene terephthalate fibers, poly-p-phenylene terephthalate fibers, poly-m-phenylene isophthalamide Examples include organic fibers such as aramid fibers, polyphenylene benzothiazole fibers, polyacrylonitrile fibers, and cellulose fibers.
補強繊維の径は3〜50μ−であり、3μm未満では分
散が困難であり好ましくない。また20μmを越えると
きは分散時に折れやすく好ましくない、補強繊維の長さ
は1〜50、好ましくは1〜25+1111である。大
部分の補強繊維がfin未満のときは組成物の補強効果
は認められない。また、50mmを越える長さでは均一
分散が困難である。The reinforcing fibers have a diameter of 3 to 50 .mu.m. If the diameter is less than 3 .mu.m, it is difficult to disperse the reinforcing fibers, which is not preferable. Further, if the reinforcing fiber exceeds 20 μm, it is undesirable because it tends to break during dispersion.The length of the reinforcing fiber is 1 to 50, preferably 1 to 25+1111. When most of the reinforcing fibers are less than fin, no reinforcing effect of the composition is observed. Further, if the length exceeds 50 mm, uniform dispersion is difficult.
補強繊維の量は20〜60、好ましくは30〜50重量
%である。20重量%未満では補強効果はあまり認めら
れず、そして60重量%を越えると組成物は脆くなるの
で好ましくない。The amount of reinforcing fibers is 20-60% by weight, preferably 30-50% by weight. If it is less than 20% by weight, the reinforcing effect will not be very noticeable, and if it exceeds 60% by weight, the composition will become brittle, which is not preferable.
本発明に用いる充填剤は、その形状がどのようなもので
あっても良い、即ち球状または球に近い形状をしている
ときは(アスペクト比が3未満のとき)内挿球の直径が
補強繊維径の約X以下である。また形状が繊維状(アス
ペクト比が3以上)であれば、その繊維径が補強繊維径
の約X以下であればよい。上記の径が分布した形状の充
填剤においては、60重量%以上好ましくは70重量%
以上が補強繊維径のX以下であればよい。The filler used in the present invention may have any shape; that is, if it is spherical or has a shape close to a sphere (when the aspect ratio is less than 3), the diameter of the inserted sphere is reinforced. The fiber diameter is approximately X or less. Further, if the shape is fibrous (aspect ratio is 3 or more), the fiber diameter may be about X or less of the reinforcing fiber diameter. In the above-mentioned filler having a shape with a distribution of diameters, 60% by weight or more, preferably 70% by weight
It is sufficient if the above is equal to or less than X of the reinforcing fiber diameter.
アスペクト比とは、球状または球状に、近い形状のとき
は短径に対する長径の比であり、繊維状のときは、繊維
径に対する繊維長の比で定義されるものである。The aspect ratio is defined as the ratio of the long axis to the short axis when the shape is spherical or nearly spherical, and the ratio of the fiber length to the fiber diameter when the shape is fibrous.
さらに該充填剤と熱可塑性樹脂との組成物の線膨張率が
熱可塑性樹脂の線膨張率の90%以下となる場合に表面
平滑性に優れた組成物となる。線膨張率は30℃から熱
可塑性樹脂の融点またはガラス転移温度よりも30℃低
い温度までの範囲で測定した値である。昇温速度は10
℃/lll1nである。Further, when the coefficient of linear expansion of the composition of the filler and the thermoplastic resin is 90% or less of the coefficient of linear expansion of the thermoplastic resin, the composition has excellent surface smoothness. The coefficient of linear expansion is a value measured in the range from 30°C to a temperature 30°C lower than the melting point or glass transition temperature of the thermoplastic resin. The heating rate is 10
℃/llll1n.
充填剤の例として、炭酸カルシウム、炭酸マグネシウム
、水酸化アルミニウム、水酸化マグネシウム、酸化亜鉛
、酸化マグネシウム、ケイ酸アルミニウム、タルク、ウ
オラストナイト、ケイ酸、ケイ酸カルシウム、ケイ酸ア
ルミニウム、マイカ、ガラスバルン、石英バルン、黒鉛
、ホウ素、アルミナ、炭化ケイ素、炭化ホウ素、ボリア
、窒化ホウ素、シリカ、ベリリウム、石英、窒化ケイ素
、酸化ベリリウム、窒化アルミニウム等の無機粉末、ア
スベスト、チタン酸カリ、炭素、黒鉛、ホウ素、アルミ
ナ、炭化ケイ素、炭化ホウ素、ボリア、窒化ホウ素、シ
リカ、ベリリウム、石英、窒化ケイ素等の無機ウィスカ
ー、マイクロセルローズ、熱硬化性樹脂の粉末、アラミ
ドパルプ、繊維補強熱可塑性樹脂組成物のマトリックス
樹脂の融点よりも高い融点を有する熱可塑性樹脂の極細
繊維、例えば極細ポリエチレンテレフタレート繊維等、
または粉末等が挙げられる。これらの充填剤を2種以上
混合して用いることもできる。Examples of fillers include calcium carbonate, magnesium carbonate, aluminum hydroxide, magnesium hydroxide, zinc oxide, magnesium oxide, aluminum silicate, talc, wollastonite, silicic acid, calcium silicate, aluminum silicate, mica, glass balloons. , quartz balloon, graphite, boron, alumina, silicon carbide, boron carbide, boria, boron nitride, silica, beryllium, quartz, silicon nitride, beryllium oxide, inorganic powders such as aluminum nitride, asbestos, potassium titanate, carbon, graphite, Inorganic whiskers such as boron, alumina, silicon carbide, boron carbide, boria, boron nitride, silica, beryllium, quartz, silicon nitride, microcellulose, thermosetting resin powder, aramid pulp, matrix of fiber reinforced thermoplastic resin composition Ultrafine fibers of thermoplastic resin having a melting point higher than the melting point of the resin, such as ultrafine polyethylene terephthalate fibers,
Or powder etc. are mentioned. Two or more of these fillers can also be used in combination.
充填剤の添加量は、繊維補強熱可塑性樹脂シートの機械
的物性等の特徴を阻害しない限りで、充填剤とマトリッ
クスとなる前記熱可塑性樹脂との組成物の線膨張率が熱
可塑性樹脂の膨張率の90%以下となる配合量であれば
良いので、マトリックスと補強繊維との組合せで好まし
い配合量は変わるが、−殻内には繊維補強熱可塑性樹脂
組成物を構成する熱可塑性樹脂と補強繊維との合計重量
が99〜50重量%、充填剤が1重量%〜50重量%、
好ましくは5重量%〜30重量%の範囲である。The amount of the filler added should be determined so that the coefficient of linear expansion of the composition of the filler and the thermoplastic resin serving as a matrix is such that the expansion coefficient of the thermoplastic resin The preferred amount varies depending on the combination of matrix and reinforcing fibers, as long as the amount is 90% or less of the fiber-reinforced thermoplastic resin composition. The total weight with fibers is 99 to 50% by weight, the filler is 1% to 50% by weight,
Preferably it is in the range of 5% to 30% by weight.
本発明の繊維補強熱可塑性樹脂組成物の製造には、種々
の公知の技術を用いることができる。Various known techniques can be used to manufacture the fiber-reinforced thermoplastic resin composition of the present invention.
たとえば、熱可塑性樹脂、補強繊維、充填剤をトライブ
レンドして押出機、ロール、バンバリーミキサ−等で混
練する方法がある。また、特開昭57−28135号公
報、特開昭58−592.24号公報等に記載されてい
るように、粉末状熱可塑性樹脂、補強繊維および充填剤
とから、抄紙法によって、繊維補強熱可塑性樹脂組成物
を製造し、インラインまたはオンラインでベルトプレス
等のホットプレスを用いて、該樹脂を溶融すると共に補
強繊維ザよび充填剤とを一体化させる方法がある。For example, there is a method in which a thermoplastic resin, reinforcing fiber, and filler are tri-blended and kneaded using an extruder, roll, Banbury mixer, or the like. In addition, as described in JP-A-57-28135, JP-A-58-592.24, etc., fiber reinforced There is a method in which a thermoplastic resin composition is produced, and the resin is melted and integrated with reinforcing fibers and a filler using an in-line or online hot press such as a belt press.
本発明の組成物に、難燃剤、熱安定剤、紫外線防止剤、
着色剤等の各種安定剤を組成物の機械的物性を損わない
範囲で添加してもよい。The composition of the present invention includes flame retardants, heat stabilizers, ultraviolet inhibitors,
Various stabilizers such as colorants may be added to the extent that the mechanical properties of the composition are not impaired.
次に本発明を実施例によって更に詳細に説明するが、こ
れに限定されるものではない、なお実施例中、部は重量
部を示す。Next, the present invention will be explained in more detail with reference to examples, but the present invention is not limited thereto. In the examples, parts indicate parts by weight.
実施例1
ポリプロピレン(溶融流れ指数Ml=4)粉末45部、
直径10μm、長さ6mmのガラス繊維30部および直
径が0.2〜0.5μ鋼のチタン酸カリウィスカー25
部を抄紙法によりシート状組成物を得た。これを200
°C,100kg/ciiの圧力下で圧縮成形法により
溶融固化して物性を測定した。Example 1 45 parts of polypropylene (melt flow index Ml = 4) powder,
30 parts of glass fiber with a diameter of 10 μm and a length of 6 mm and 25 parts of potassium titanate whiskers of steel with a diameter of 0.2-0.5 μm
A sheet-like composition was obtained by a papermaking method. This is 200
The material was melted and solidified by compression molding at 100 kg/cii at a temperature of 100 kg/cii, and its physical properties were measured.
特性を表に示す、なお、ポリプロピレン樹脂とチタン酸
カリウムウィスカーとの組成物を抄紙法で製造し線膨張
率を測定した結果40 X 10− hcm/cm・℃
であり、ポリプロピレンの線膨張率は230 X 10
− ’cm / cm・°Cの17%であった。表面平
滑性は像鮮明度により評価した。値が大きいほど表面平
滑性が優れている。The properties are shown in the table. A composition of polypropylene resin and potassium titanate whiskers was produced by a papermaking method and the coefficient of linear expansion was measured to be 40 x 10-hcm/cm・℃.
and the coefficient of linear expansion of polypropylene is 230 x 10
−'cm/cm·°C was 17%. Surface smoothness was evaluated by image clarity. The larger the value, the better the surface smoothness.
比較例1
実施例1と同様の方法でポリプロピレン粉末60部、ガ
ラス繊維(直径10μs+、長さ6mm)40部からな
る溶融固化シートを作製した。特性を表に示す。Comparative Example 1 A melt-solidified sheet consisting of 60 parts of polypropylene powder and 40 parts of glass fiber (diameter 10 μs+, length 6 mm) was produced in the same manner as in Example 1. The characteristics are shown in the table.
実施例2
ポリエチレンテレフタレート粉末49部、直径lOμm
、長さ13ffi11のガラス繊維21部、直径が0.
05〜0.5μmの炭素質ウィスカー30部を抄紙法に
よりマットを作製し、次いで300 ’C,100kg
/cdの圧力下で圧縮成形法により溶融固化シートとし
た。特性を表に示す。ポリエチレンテレフタレートと炭
素質ウィスカーとの組成物の線膨張率は45 X 10
− ’cm/cm・”Cであり、ポリエチレンテレフタ
レート樹脂の線膨張率200X10−hcm/cm・℃
のに3%であった。Example 2 49 parts of polyethylene terephthalate powder, diameter 10 μm
, 21 parts of glass fiber of length 13ffi11, diameter 0.
A mat was prepared from 30 parts of carbonaceous whiskers of 0.05 to 0.5 μm by a papermaking method, and then heated at 300'C and 100kg.
A melt-solidified sheet was formed by compression molding under a pressure of /cd. The characteristics are shown in the table. The linear expansion coefficient of the composition of polyethylene terephthalate and carbonaceous whiskers is 45 x 10
- 'cm/cm・''C, and the linear expansion coefficient of polyethylene terephthalate resin is 200X10-hcm/cm・℃
However, it was 3%.
比較例2
炭素質ウィスカーを含まない実施例2の組成で溶融固化
シートを作製した。特性を表に示す。Comparative Example 2 A melt-solidified sheet was produced using the composition of Example 2, which did not contain carbonaceous whiskers. The characteristics are shown in the table.
実施例3
ポリプロピレン(MI=4)粉末54部、直径10μm
、長さ13鴫のガラス繊維36部および平均粒子径が1
μmである水酸化アルミニウム粉末10部を実施例1と
同様の方法で溶融固化シートを作製した。特性を表に示
す。ポリプロピレンと水酸化アルミニウムとの組成物の
線膨張率は、160X 10−’cm/cm・”Cであ
り、ポリプロピレン樹脂の線膨張率230 X 10−
’C1l/e1m ・’Cの70%であった。Example 3 54 parts of polypropylene (MI=4) powder, diameter 10 μm
, 36 parts of glass fiber with a length of 13 mm and an average particle size of 1
A sheet was melted and solidified using the same method as in Example 1 using 10 parts of aluminum hydroxide powder having a diameter of μm. The characteristics are shown in the table. The linear expansion coefficient of the composition of polypropylene and aluminum hydroxide is 160 x 10-'cm/cm・''C, and the linear expansion coefficient of the polypropylene resin is 230 x 10-'
'C1l/e1m 70% of 'C.
比較例3
水酸化アルミニウム粉末として平均粒子径が3.5μm
の粉末を用いた以外は実施例3と同一の組成で溶融固化
シートを作製した。特性を表に示す。Comparative Example 3 Aluminum hydroxide powder with an average particle size of 3.5 μm
A melt-solidified sheet was produced with the same composition as in Example 3 except that the powder was used. The characteristics are shown in the table.
実施例4
ポリプロピレン(MI=4)粉末45部、直径6μm、
長さ13IIIfllのガラス繊維50部および平均粒
子径が0.4μmであるハードクレー型カオリンクレー
5部を実施例1と同様の方法で溶融固化シートを作製し
た。特性を表に示す。ポリプロピレンとハードクレー型
カオリンクレーとの組成物の線膨張率は195 X 1
0− ’cm/cu+ ・”Cであり、ポリプロピレン
樹脂の線膨張率230X10−6cm/cm・”Cの8
5%であった。Example 4 45 parts of polypropylene (MI=4) powder, diameter 6 μm,
A melt-solidified sheet was prepared in the same manner as in Example 1 using 50 parts of glass fiber having a length of 13III full and 5 parts of hard clay type kaolin clay having an average particle diameter of 0.4 μm. The characteristics are shown in the table. The linear expansion coefficient of the composition of polypropylene and hard clay type kaolin clay is 195 x 1
0-'cm/cu+ ・"C, and the linear expansion coefficient of polypropylene resin is 230 x 10-6cm/cm・"C 8
It was 5%.
比較例4
ハードクレー型カオリンクレーを含まない実施例2の組
成で溶融固化シートを作製した。特性を表に示す。Comparative Example 4 A melt-solidified sheet was produced using the composition of Example 2, which did not contain hard clay-type kaolin clay. The characteristics are shown in the table.
以下余白
〔発明の効果〕
本発明によれば、特定の大きさの充填剤で、かつ充填剤
と熱可塑性樹脂との組成物の線膨張率が熱可塑性樹脂の
線膨張率の90%以下となるように充填剤を添加するこ
とによって、極めて容易に表面平滑性に優れた組成物を
得ることができる。Blank below [Effects of the Invention] According to the present invention, the filler has a specific size and the linear expansion coefficient of the composition of the filler and the thermoplastic resin is 90% or less of the linear expansion coefficient of the thermoplastic resin. By adding a filler in such a manner that a composition with excellent surface smoothness can be obtained very easily.
従って表面平滑性が望まれている分野の製品、例えば自
動車用外板、産業用および民生用機器類で外に出る部分
等の製品として有用である。また、表面平滑性を向上さ
せるための種々の後加工、例えばコーティング、フィル
ムの積層、成形金型温度の高温化等が不要となりコスト
が安くなる効果もある。Therefore, it is useful for products in fields where surface smoothness is desired, such as exterior panels for automobiles, and external parts of industrial and consumer equipment. In addition, various post-processing to improve surface smoothness, such as coating, lamination of films, and raising the temperature of the molding die, are not required, resulting in lower costs.
特許出願人 旭化成工業株式会社Patent applicant: Asahi Kasei Industries, Ltd.
Claims (1)
20μm、繊維長1〜50mmの補強繊維60〜20重
量%からなる組成物、99〜50重量%と(B)充填剤
、1〜50重量%とからなり、(C)前記充填剤のアス
ペクト比が3未満のときは、その内挿球の直径が、また
、同アスペクト比が3以上のときはその繊維径が前記補
強繊維径のに以下であり、かつ、(D)前記充填剤と前
記熱可塑性樹脂との2成分の組成物の線膨張率が前記熱
可塑性樹脂の線膨張率の90%以下となるような組成比
で前記充填剤を含有することを特徴とする表面平滑性に
優れた繊維補強熱可塑性樹脂組成物(A) Thermoplastic resin 40-80% by weight and fiber diameter 3-80% by weight
A composition consisting of 60 to 20% by weight of reinforcing fibers of 20 μm and a fiber length of 1 to 50 mm, 99 to 50% by weight, and (B) a filler, 1 to 50% by weight, and (C) an aspect ratio of the filler. is less than 3, the diameter of the interpolated sphere, and when the aspect ratio is 3 or more, the fiber diameter is less than or equal to the reinforcing fiber diameter, and (D) the filler and the Excellent surface smoothness characterized by containing the filler in a composition ratio such that the coefficient of linear expansion of the two-component composition with a thermoplastic resin is 90% or less of the coefficient of linear expansion of the thermoplastic resin. Fiber-reinforced thermoplastic resin composition
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21849588A JPH0267326A (en) | 1988-09-02 | 1988-09-02 | Fiber-reinforced thermoplastic resin composition with excellent surface flatness |
EP19890909853 EP0386266A4 (en) | 1988-09-02 | 1989-09-01 | Fiber-reinforced thermoplastic resin sheet or pellet |
PCT/JP1989/000904 WO1990002642A1 (en) | 1988-09-02 | 1989-09-01 | Fiber-reinforced thermoplastic resin sheet or pellet |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21849588A JPH0267326A (en) | 1988-09-02 | 1988-09-02 | Fiber-reinforced thermoplastic resin composition with excellent surface flatness |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0267326A true JPH0267326A (en) | 1990-03-07 |
JPH0411579B2 JPH0411579B2 (en) | 1992-02-28 |
Family
ID=16720827
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21849588A Granted JPH0267326A (en) | 1988-09-02 | 1988-09-02 | Fiber-reinforced thermoplastic resin composition with excellent surface flatness |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0267326A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0429407U (en) * | 1990-07-06 | 1992-03-10 | ||
JPH0570688A (en) * | 1991-03-05 | 1993-03-23 | Polyplastics Co | Reinforced polyarylene sulfide resin composition and its molded product |
JPH10324784A (en) * | 1997-03-27 | 1998-12-08 | Kuraray Co Ltd | Thermally melting polyvinyl alcoholic resin composition |
US5918458A (en) * | 1997-02-14 | 1999-07-06 | General Electric Company | System and method of providing clean filtered cooling air to a hot portion of a gas turbine engine |
WO2005036521A1 (en) * | 2003-10-14 | 2005-04-21 | Kabushiki Kaisha Kawai Gakki Seisakusho | Repetition lever of grand piano |
JP2009270057A (en) * | 2008-05-09 | 2009-11-19 | Asahi Kasei Chemicals Corp | Glass filament-reinforced polyamide resin composition, resin pellet, and molded product therefrom |
CN102558666A (en) * | 2010-12-28 | 2012-07-11 | 上海金发科技发展有限公司 | Ceramic fiber reinforced polypropylene complex and preparation method thereof |
CN102757598A (en) * | 2011-04-29 | 2012-10-31 | 上海金发科技发展有限公司 | Ceramic-fiber-reinforced aging-resistant polypropylene complex and preparation method thereof |
-
1988
- 1988-09-02 JP JP21849588A patent/JPH0267326A/en active Granted
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0429407U (en) * | 1990-07-06 | 1992-03-10 | ||
JPH0570688A (en) * | 1991-03-05 | 1993-03-23 | Polyplastics Co | Reinforced polyarylene sulfide resin composition and its molded product |
US5918458A (en) * | 1997-02-14 | 1999-07-06 | General Electric Company | System and method of providing clean filtered cooling air to a hot portion of a gas turbine engine |
JPH10324784A (en) * | 1997-03-27 | 1998-12-08 | Kuraray Co Ltd | Thermally melting polyvinyl alcoholic resin composition |
WO2005036521A1 (en) * | 2003-10-14 | 2005-04-21 | Kabushiki Kaisha Kawai Gakki Seisakusho | Repetition lever of grand piano |
US7678977B2 (en) | 2003-10-14 | 2010-03-16 | Kabushiki Kaisha Kawai Gakki Seisakusho | Repetition lever of grand piano |
JP2009270057A (en) * | 2008-05-09 | 2009-11-19 | Asahi Kasei Chemicals Corp | Glass filament-reinforced polyamide resin composition, resin pellet, and molded product therefrom |
CN102558666A (en) * | 2010-12-28 | 2012-07-11 | 上海金发科技发展有限公司 | Ceramic fiber reinforced polypropylene complex and preparation method thereof |
CN102757598A (en) * | 2011-04-29 | 2012-10-31 | 上海金发科技发展有限公司 | Ceramic-fiber-reinforced aging-resistant polypropylene complex and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0411579B2 (en) | 1992-02-28 |
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