JPH03282198A - Shaft - Google Patents
ShaftInfo
- Publication number
- JPH03282198A JPH03282198A JP8237990A JP8237990A JPH03282198A JP H03282198 A JPH03282198 A JP H03282198A JP 8237990 A JP8237990 A JP 8237990A JP 8237990 A JP8237990 A JP 8237990A JP H03282198 A JPH03282198 A JP H03282198A
- Authority
- JP
- Japan
- Prior art keywords
- prepreg
- film
- fiber
- straightness
- resin
- 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.)
- Pending
Links
- 239000003822 epoxy resin Substances 0.000 claims abstract description 16
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 14
- 239000011347 resin Substances 0.000 claims abstract description 14
- 239000011159 matrix material Substances 0.000 claims abstract description 9
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 8
- 238000010030 laminating Methods 0.000 claims description 4
- 239000012783 reinforcing fiber Substances 0.000 abstract description 6
- 229920001971 elastomer Polymers 0.000 abstract description 4
- 239000000806 elastomer Substances 0.000 abstract description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 abstract description 4
- 238000012937 correction Methods 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 238000003825 pressing Methods 0.000 abstract description 3
- 239000000835 fiber Substances 0.000 description 16
- 230000009849 deactivation Effects 0.000 description 14
- 238000001723 curing Methods 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 7
- 229920000049 Carbon (fiber) Polymers 0.000 description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 5
- 239000004917 carbon fiber Substances 0.000 description 5
- 239000003733 fiber-reinforced composite Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000004804 winding Methods 0.000 description 4
- 238000009499 grossing Methods 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 230000037303 wrinkles Effects 0.000 description 3
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 2
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 2
- 235000017491 Bambusa tulda Nutrition 0.000 description 2
- 241001330002 Bambuseae Species 0.000 description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000011425 bamboo Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000002779 inactivation Effects 0.000 description 2
- VYKXQOYUCMREIS-UHFFFAOYSA-N methylhexahydrophthalic anhydride Chemical compound C1CCCC2C(=O)OC(=O)C21C VYKXQOYUCMREIS-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- ITNADJKYRCCJNX-UHFFFAOYSA-N 3-(2,3-diaminophenyl)sulfonylbenzene-1,2-diamine Chemical compound NC1=CC=CC(S(=O)(=O)C=2C(=C(N)C=CC=2)N)=C1N ITNADJKYRCCJNX-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- CXXSQMDHHYTRKY-UHFFFAOYSA-N 4-amino-2,3,5-tris(oxiran-2-ylmethyl)phenol Chemical compound C1=C(O)C(CC2OC2)=C(CC2OC2)C(N)=C1CC1CO1 CXXSQMDHHYTRKY-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- IGALFTFNPPBUDN-UHFFFAOYSA-N phenyl-[2,3,4,5-tetrakis(oxiran-2-ylmethyl)phenyl]methanediamine Chemical compound C=1C(CC2OC2)=C(CC2OC2)C(CC2OC2)=C(CC2OC2)C=1C(N)(N)C1=CC=CC=C1 IGALFTFNPPBUDN-UHFFFAOYSA-N 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
の1
本発明は、繊維強化複合樹脂管にて形成される矢に関す
るものであり、特に、複層プリプレグを複数層積層し一
体としたことを特徴とする失活(矢の細部)に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION 1. The present invention relates to an arrow made of a fiber-reinforced composite resin pipe, and particularly relates to an arrow made of a fiber-reinforced composite resin pipe, and in particular, an arrow made of a deactivated ( details of the arrow).
【未亘且I
従来、例えば矢の軸部、即ち、失活は、竹などで作製さ
れていたが、近年、第2図に図示されるように、軽量で
且つ機械的強度が高いという理由から、強化繊維として
炭素繊維或はガラス繊維を用いた繊維強化複合樹脂材1
01を管形状に成形することにより作製することが提案
され、実用化されている。Previously, for example, the shaft of an arrow, that is, the deactivation shaft, was made of bamboo, but in recent years, as shown in Figure 2, it has been made of bamboo because it is lightweight and has high mechanical strength. From, fiber reinforced composite resin material 1 using carbon fiber or glass fiber as reinforcing fiber
01 into a tube shape has been proposed and put into practical use.
斯る失活は、マンドレルに繊維強化プリプレグを所定枚
数だけ巻き付け、硬化することによって作製される。Such deactivation is produced by winding a predetermined number of fiber-reinforced prepregs around a mandrel and curing them.
が よ と る
しかしながら、このような材料及び製造方法にて作製さ
れた繊維強化複合材料製の失活は、プリプレグの硬化時
に僅かに変形し、真直性に問題が発生することがあった
。又、−互変形した失活は、外表面を研磨することによ
り修正することもできるが、このような修正加工は極め
て困難であるか、例え、修正加工により真直性が修正で
きたとしても、失活の長さ方向の肉厚に変化が起こり、
バランスの点で問題が発生することがあった。However, deactivation plates made of fiber-reinforced composite materials produced using such materials and manufacturing methods may be slightly deformed during curing of the prepreg, resulting in problems with straightness. In addition, deactivation caused by deformation can be corrected by polishing the outer surface, but such correction processing is extremely difficult, or even if the straightness can be corrected by correction processing, Changes occur in the wall thickness along the length of the inactivation,
Sometimes there were problems with balance.
従って、成形加工性の向上、更には美感上の点からも一
層の改良が望まれている。Therefore, further improvements are desired from the viewpoint of improving moldability and aesthetics.
本発明者らは、多くの研究実験を行った結果、プリプレ
グの表面に、溶解度パラメータが9゜0〜11.5の熱
可塑性樹脂フィルムを設けて構成される複層プリプレグ
層を積層して管状に成形し、矢を作製した場合には、真
直性が極めて良好に達成され、又、例え、僅かに真直性
が狂っていた場合においても、バランスを崩すことなく
簡単に真直性の修正が可能であることを見出した。更に
、前記熱可塑性樹脂フィルムは、特に熱可塑性ウレタン
エラストマーが好ましいことも分かった。As a result of many research experiments, the present inventors discovered that a tubular shape was obtained by laminating multilayer prepreg layers consisting of a thermoplastic resin film with a solubility parameter of 9°0 to 11.5 on the surface of prepreg. When an arrow is made by molding the arrow, very good straightness is achieved, and even if the straightness is slightly out of order, the straightness can be easily corrected without losing balance. I found that. Furthermore, it has been found that thermoplastic urethane elastomer is particularly preferable for the thermoplastic resin film.
本発明は斯かる新規な知見に基づきなされたものである
。The present invention has been made based on this new knowledge.
従って1本発明の目的は、真直性が極めて良好に達成さ
れ、又、例え、僅かに真直性が狂っていた場合において
も、バランスを崩すことなく簡単に真直性の修正が可能
であって、成形加工性が良好であり、しかも、折損防止
及び美感上の点からも改良された失活な提供することで
ある。Therefore, one object of the present invention is to achieve extremely good straightness, and even if the straightness is slightly out of order, it is possible to easily correct the straightness without losing balance. It is an object of the present invention to provide a deactivated material that has good moldability and is improved in terms of breakage prevention and aesthetics.
るための 上記目的は本発明に係る失活にて達成される。for The above object is achieved by the inactivation according to the present invention.
要約すれば本発明は、マトリクス樹脂としてエポキシ樹
脂を使用した繊維強化プリプレグの表面に、溶解度パラ
メータが9.0〜11.5の熱可塑性樹樹脂フィルムを
設けて構成される複層プリプレグを積層し、一体とする
ことによって形成されることを特徴とする失活である。In summary, the present invention laminates a multilayer prepreg formed by providing a thermoplastic resin film with a solubility parameter of 9.0 to 11.5 on the surface of a fiber-reinforced prepreg using an epoxy resin as a matrix resin. , is a deactivation characterized by being formed by integrating.
好ましくは、前記熱可塑性樹脂フィルムは、熱可塑性ウ
レタンエラストマーとされる。Preferably, the thermoplastic resin film is a thermoplastic urethane elastomer.
更に説明すると、本発明に係る失活は、第1図に図示さ
れるように、複層プリプレグ層1°が複数層積層し、一
体化することによって形成される。該複層プリプレグ層
1°は、本発明の特徴とする複層プリプレグl°をマン
ドレルに複数枚巻き付けることによって、或は連続して
複数回巻き付けることによって積層し、次いで硬化する
ことによって、形成される。To explain further, the deactivation according to the present invention is formed by laminating a plurality of 1° multilayer prepreg layers and integrating them, as shown in FIG. The multi-layer prepreg layer 1° is formed by winding a plurality of multi-layer prepreg l°, which is a feature of the present invention, around a mandrel, or by laminating the multi-layer prepreg l° by continuously winding it several times, and then curing it. Ru.
夾」L泗
第3図に、本発明に係る複層プリプレグ層1゜を形成す
るために使用される複層プリプレグlの一実施例が示さ
れる。FIG. 3 shows an embodiment of a multi-layer prepreg l used to form a multi-layer prepreg layer 1 according to the present invention.
本実施例によると、複層プリプレグ1は、強化繊維2と
マトリクス樹脂4からなる繊維強化プリプレグ6の上に
溶解度パラメータが9.0〜11.5の熱可塑性樹樹脂
フィルム、特に好ましくは熱可塑性ウレタンエラストマ
ーフィルム8が設けられる。According to this embodiment, the multilayer prepreg 1 is made of a thermoplastic resin film having a solubility parameter of 9.0 to 11.5, particularly preferably a thermoplastic A urethane elastomer film 8 is provided.
フィルム8の厚さは5〜1100u程度とされる。上記
フィルムの厚さが1100LLを超えると、靭性及び衝
撃吸収特性は向上するが、他の機械的強度、即ち引張強
度、圧縮強度、弾性率などの強度低下が無視し得なくな
る。又、フィルム8の厚さが5μm未満であると薄(な
り過ぎ、詳しくは後述するが、失活成形後の外表面の後
加工処理が困難となる。The thickness of the film 8 is approximately 5 to 1100 u. When the thickness of the film exceeds 1100 LL, the toughness and shock absorption properties are improved, but the decrease in other mechanical strengths, such as tensile strength, compressive strength, and elastic modulus, becomes unignorable. Further, if the thickness of the film 8 is less than 5 μm, it becomes too thin, and as will be described in detail later, post-processing of the outer surface after deactivation molding becomes difficult.
本発明において、複層プリプレグ1に使用される強化繊
維としては、通常炭素繊維が使用されるが、他の強化繊
維、例えばガラス繊維、その他、ボロン繊維、アルミナ
繊維、炭化珪素繊維、窒化珪素繊維などの無機繊維、或
はアラミド繊維、ボリアリレート繊維、ポリエチレン繊
維などの種々の有機繊維、更には、チタン繊維、アモル
ファス繊維、ステンレススチール繊維、アルミニウム繊
維などの金属繊維を好適に使用し得る。In the present invention, the reinforcing fiber used in the multilayer prepreg 1 is usually carbon fiber, but other reinforcing fibers such as glass fiber, boron fiber, alumina fiber, silicon carbide fiber, and silicon nitride fiber can also be used. Various organic fibers such as aramid fibers, polyarylate fibers, polyethylene fibers, and metal fibers such as titanium fibers, amorphous fibers, stainless steel fibers, and aluminum fibers can be suitably used.
マトリクス樹脂としては、エポキシ樹脂が好適であり、
更に、硬化温度が50〜200℃となるように硬化剤そ
の他の付与剤、例えば可撓性付与剤などが適当に添加さ
れる。Epoxy resin is suitable as the matrix resin,
Further, a curing agent and other imparting agents, such as a flexibility imparting agent, are appropriately added so that the curing temperature is 50 to 200°C.
エポキシ樹脂としての好ましい一例を挙げれば、例えば
、(1)グリシジルエーテル系エポキシ樹脂(ビスフェ
ノールA、F、S系エポキシ樹脂、ノボラック系エポキ
シ樹脂、臭素化ビスフェノールA系エポキシ樹脂);
(2)環式脂肪族エポキシ樹脂; (3)グリシジル
エステル系エポキシ樹脂; (4)グリシジルアミン系
エポキシ樹脂(テトラグリシジルジアミノジフェニルメ
タン、トリグリシジル−p−アミノフェノールなど);
(5)複素環式エポキシ樹脂;その他種々のエポキシ樹
脂から選択される1種又は複数種が使用され、特に、ビ
スフェノールA、F、Sグリシジルアミン系エポキシ樹
脂が好適に使用される。又、硬化剤としてはアミン系硬
化剤、例えばジシアンジアミド(D I CY) ジ
アミノフェニルスルフォン(DDS) ジアミノジフ
ェニルメタン(DDM);酸無水物系、例えばヘキサヒ
ドロ無水フタル酸(HHPA) 、メチルへキサヒドロ
無水フタル酸(MHHPA)などが使用されるが、特に
アミン系硬化剤が好適に使用される。Preferred examples of the epoxy resin include (1) glycidyl ether-based epoxy resin (bisphenol A, F, S-based epoxy resin, novolac-based epoxy resin, brominated bisphenol A-based epoxy resin);
(2) Cycloaliphatic epoxy resin; (3) Glycidyl ester-based epoxy resin; (4) Glycidylamine-based epoxy resin (tetraglycidyldiaminodiphenylmethane, triglycidyl-p-aminophenol, etc.);
(5) Heterocyclic epoxy resin: One or more types selected from various other epoxy resins are used, and bisphenol A, F, and S glycidylamine-based epoxy resins are particularly preferably used. Further, as the curing agent, amine-based curing agents such as dicyandiamide (DICY), diaminophenyl sulfone (DDS), diaminodiphenylmethane (DDM); acid anhydride-based curing agents such as hexahydrophthalic anhydride (HHPA), methylhexahydrophthalic anhydride; (MHHPA) and the like are used, and amine-based curing agents are particularly preferably used.
本発明に係る失活の一実施例を示せば次のとおりである
。An example of deactivation according to the present invention is as follows.
先ず、所定の形状寸法に裁断した上記複層プリプレグ1
(複層プリプレグ層1°)がマンドレルに巻き付けられ
る。このとき、フィルム8が最外表面に位置するように
される。First, the multilayer prepreg 1 cut into a predetermined shape and size.
(multilayer prepreg layer 1°) is wrapped around a mandrel. At this time, the film 8 is positioned on the outermost surface.
このようにしてマンドレル上に巻き付けられたプリプレ
グ積層体の上に、押さえテープを巻回し、その後、押さ
えテープによりプリプレグ層の変形を防止しながらプリ
プレグ積層体を加熱、硬化し、失活を得る。A pressure tape is wound on the prepreg laminate thus wound on the mandrel, and then the prepreg laminate is heated and cured to obtain deactivation while the pressure tape prevents deformation of the prepreg layer.
硬化後、失活表面から押さえテープを取り除いたのち、
加熱硬化時に押さえテープにより生じたプリプレグ硬化
体表面のシワを除去する平滑加工を行なう、この平滑加
工は、得られた失活表面を形成しているフィルム8を加
熱し、シワを伸ばすように押圧することにより行われ、
容易にシワをフィルムに吸収して除去できる。必要に応
じて、同時に、或は、平滑加工後に、加熱しなから失活
の真直性が調整される。After curing, after removing the pressure tape from the deactivated surface,
A smoothing process is performed to remove wrinkles on the surface of the cured prepreg product caused by the pressing tape during heat curing. This smoothing process involves heating the film 8 forming the obtained deactivated surface and pressing it to smooth out the wrinkles. It is done by
Wrinkles can be easily absorbed into the film and removed. If necessary, at the same time or after smoothing, the straightness of the deactivation is adjusted without heating.
又、フィルム8が透明とされる場合には、失活表面に装
飾性を付与することができる。即ち、複層プリプレグ1
において、例えば炭素繊維及びその他の異種繊維を一方
向に配列して強化繊維としたときには、これら異種繊維
が表面から透けて見えることとなり、失活の表面の装飾
性を一段と向上することができる。なお、ポリウレタン
樹脂のフィルムによれば、従来のように塗装によってプ
リプレグ硬化体に表面の装飾性を持たせることも可能で
ある。Moreover, when the film 8 is made transparent, decorative properties can be imparted to the deactivated surface. That is, multilayer prepreg 1
For example, when carbon fibers and other different types of fibers are arranged in one direction to form reinforcing fibers, these different types of fibers can be seen through the surface, and the decorativeness of the deactivated surface can be further improved. In addition, according to the polyurethane resin film, it is also possible to give the surface of the cured prepreg body decorative properties by painting as in the conventional manner.
実際に、強化繊維2として、繊維径が6.5μmとされ
るPAN系の炭素繊維(東し株式会社製:商品名rM4
0J)を使用し、マトリクス樹脂はエポキシ樹脂を使用
して炭素繊維強化プリプレグ6を作製し、この表面に、
厚さ5μm、溶解度パラメータ1O00の熱可塑性ウレ
タンエラストマーフィルム8を貼り付けることにより、
複層プリプレグ1を作製した。溶解度パラメータは溶媒
に対する溶解性から決定した。該プリプレグ1のマトリ
クス樹脂含有量は35重量%であり、厚さはフィルム8
を除いて50μmであった。In fact, as the reinforcing fiber 2, a PAN-based carbon fiber with a fiber diameter of 6.5 μm (manufactured by Toshi Co., Ltd., product name rM4) was used.
0J), a carbon fiber reinforced prepreg 6 was prepared using epoxy resin as the matrix resin, and on this surface,
By pasting a thermoplastic urethane elastomer film 8 with a thickness of 5 μm and a solubility parameter of 1000,
Multilayer prepreg 1 was produced. The solubility parameter was determined from the solubility in the solvent. The matrix resin content of the prepreg 1 is 35% by weight, and the thickness is 8% by weight.
It was 50 μm except for.
又、このような複層プリプレグ1を、積層数が5層とな
るように連続的にマンドレルに巻き付けることにより、
第1図に図示される構造の失活を有した矢を製造した。In addition, by continuously winding such multilayer prepreg 1 around a mandrel so that the number of laminated layers is 5,
Arrows with deactivation of the structure illustrated in FIG. 1 were manufactured.
該矢の機械的特性などを測定したが、本発明に係る矢は
軽量であるにも拘らず機械的強度も十分であり、しかも
第2図に示す従来の矢に比較して、高度の真直性を有し
ており、又、成形加工性も優れていた。更に、本発明に
従った矢は、美感的にも好ましいものであった。測定結
果を表1に示す。The mechanical properties of the arrow were measured, and it was found that the arrow according to the present invention has sufficient mechanical strength despite being lightweight, and has a higher degree of straightness than the conventional arrow shown in Fig. 2. It also had excellent moldability. Additionally, arrows according to the invention were aesthetically pleasing. The measurement results are shown in Table 1.
表1
一:比較例1より劣る
注:ポリプロピレン樹脂の溶解度パラメータは8.1で
あった。Table 1 1: Inferior to Comparative Example 1 Note: The solubility parameter of the polypropylene resin was 8.1.
!」Lの」L里
以上説明したように構成される本発明に係る矢は、軽量
で機械的強度もあり、高度の真直性を有しており、又、
成形加工性も優れていた。更に、本発明に従った矢は、
美感的にも好ましく、靭性もあり、折れ難いという特長
も有している。! The arrow according to the present invention constructed as described above is lightweight, has mechanical strength, and has a high degree of straightness.
The moldability was also excellent. Furthermore, the arrow according to the invention is
It is aesthetically pleasing, has toughness, and has the characteristics of not easily breaking.
第1図は、本発明に係る失活の横断面図である。
第2図は、従来の失活の横断面図である。
第3図は、本発明に係る失活を製造するための複層プリ
プレグの実施例の断面図である。
1° :複層プリプレグ層
101:繊維強化複合樹脂管
1:複層プリプレグ
2:強化繊維
4:マトリクス樹脂
8:フィルムFIG. 1 is a cross-sectional view of a deactivation device according to the present invention. FIG. 2 is a cross-sectional view of a conventional deactivation. FIG. 3 is a cross-sectional view of an embodiment of a multilayer prepreg for producing a deactivation according to the present invention. 1°: Multilayer prepreg layer 101: Fiber-reinforced composite resin pipe 1: Multilayer prepreg 2: Reinforced fiber 4: Matrix resin 8: Film
Claims (1)
強化プリプレグの表面に、溶解度パラメータが9.0〜
11.5の熱可塑性樹脂フィルムを設けて構成される複
層プリプレグを積層し、一体とすることによって形成さ
れることを特徴とする矢柄。1) The surface of the fiber-reinforced prepreg using epoxy resin as the matrix resin has a solubility parameter of 9.0~
An arrow shaft characterized in that it is formed by laminating and integrating multilayer prepregs each having a thermoplastic resin film of 11.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8237990A JPH03282198A (en) | 1990-03-29 | 1990-03-29 | Shaft |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8237990A JPH03282198A (en) | 1990-03-29 | 1990-03-29 | Shaft |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03282198A true JPH03282198A (en) | 1991-12-12 |
Family
ID=13772949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8237990A Pending JPH03282198A (en) | 1990-03-29 | 1990-03-29 | Shaft |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03282198A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101335754B1 (en) * | 2011-03-07 | 2013-12-02 | 송문재 | An arrow body with dimples and manufacturing method of the same |
-
1990
- 1990-03-29 JP JP8237990A patent/JPH03282198A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101335754B1 (en) * | 2011-03-07 | 2013-12-02 | 송문재 | An arrow body with dimples and manufacturing method of the same |
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