JP4850551B2 - Conveyor shaft - Google Patents

Conveyor shaft Download PDF

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JP4850551B2
JP4850551B2 JP2006078883A JP2006078883A JP4850551B2 JP 4850551 B2 JP4850551 B2 JP 4850551B2 JP 2006078883 A JP2006078883 A JP 2006078883A JP 2006078883 A JP2006078883 A JP 2006078883A JP 4850551 B2 JP4850551 B2 JP 4850551B2
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resin composition
glass
thermosetting resin
shaft
agent
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JP2007255507A (en
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二治男 小和田
信彦 内田
安芳 竹澤
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Kyocera Chemical Corp
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Description

本発明は、エッチング装置内でプリント基板等の搬送に用いられる搬送用シャフトに関し、特に、耐薬品性、エッチング温度、スプレー圧力への耐性等のエッチング条件に対して優れた耐性を有し、軽量な搬送用シャフトに関する。   The present invention relates to a transport shaft used for transporting a printed circuit board or the like in an etching apparatus, and in particular, has excellent resistance to etching conditions such as resistance to chemicals, etching temperature and spray pressure, and is lightweight. The present invention relates to a transport shaft.

エッチング装置は、プリント基板、液晶、シャドーマスク等電子部品用途の微細加工に幅広く使われているが、金属を連続的に溶かして加工するものであるため、装置の処理部に求められる特性は、耐酸性、耐アルカリ性、耐有機薬品性が求められ、またエッチング液の温度、スプレー圧力への耐性も要求される。   Etching equipment is widely used for microfabrication of electronic parts such as printed circuit boards, liquid crystals, shadow masks, etc., but since the metal is continuously melted and processed, the characteristics required for the processing part of the equipment are as follows: Acid resistance, alkali resistance and organic chemical resistance are required, and resistance to etching solution temperature and spray pressure is also required.

特に、エッチング槽内で製品を連続的に搬送するための搬送用シャフトは、駆動軸も兼ねるため、上記の特性に加え、長期間のスムースな回転力を維持する製品信頼性も求められる。さらに、製品の軽薄化、大型化に伴い、搬送シャフトの軽量化に加え、たわみ等を抑制する形状安定性も求められる。   In particular, since the conveying shaft for continuously conveying the product in the etching tank also serves as the drive shaft, in addition to the above characteristics, a product reliability that maintains a long-term smooth rotational force is also required. Furthermore, as the products become lighter and larger, in addition to reducing the weight of the transport shaft, shape stability that suppresses deflection and the like is also required.

従来の搬送用シャフトは、剛性の高い金属にエポキシ樹脂を被覆して耐薬品性を施した構造材を用いることが一般的であったが、軽量化を目的として、カーボン繊維を基材としてエポキシ樹脂により成形した引抜成形製品も使用されるようになってきている。   Conventional transport shafts typically use structural materials that are chemically resistant by coating a highly rigid metal with an epoxy resin. However, for the purpose of weight reduction, epoxy is used with carbon fiber as the base material. A pultruded product molded from a resin has also been used.

しかしながら、カーボン繊維の市場の活性化は、さらに拡大する方向にあり、特に引抜成形製品用カーボン繊維は、その求められる耐薬品性が特殊なため入手困難であり、価格も高騰している。このような中、耐薬品性に優れたガラス繊維が開発され、下水道、浄化槽や鉄筋代替FRPロッド用に応用が期待されている(例えば、特許文献1参照。)。
特開2002−60252号公報
However, the activation of the carbon fiber market is in the direction of further expansion. In particular, carbon fibers for pultruded products are difficult to obtain due to their special chemical resistance, and the price is also rising. Under such circumstances, glass fibers excellent in chemical resistance have been developed and are expected to be applied to sewers, septic tanks and reinforcing steel substitute FRP rods (for example, see Patent Document 1).
JP 2002-60252 A

エッチング装置に用いる搬送用シャフトは、耐アルカリ性、耐酸性等の耐薬品性が要求される部品であるが、カーボン繊維に代わる繊維がなかったため、これを用いていない不飽和ポリエステル系、ビニルエステル系樹脂の引抜成形製品は、耐薬品性を満足することができなかった。   The transport shaft used in the etching equipment is a part that requires chemical resistance such as alkali resistance and acid resistance, but there was no fiber to replace carbon fiber, so unsaturated polyester and vinyl ester systems that do not use this The resin pultruded product could not satisfy the chemical resistance.

そのため、このような搬送シャフトは、樹脂ワレ、変形が起こり、それに伴って生ずる搬送時の回転ムラにより搬送製品をキズ付けたり、搬送中に製品が引っかかり搬送を円滑に行えない、等の問題が発生していた。   For this reason, such a conveyance shaft has problems such as resin cracking, deformation, scratches on the conveyance product due to uneven rotation during conveyance, and the product being caught during conveyance and not being able to smoothly convey. It has occurred.

そこで、本発明は、耐薬品性に優れ、搬送を円滑に行うことができることに加え、軽量化を施したエッチング装置用として好適な搬送用シャフトを提供することを目的とするものである。   Therefore, the present invention has an object to provide a transport shaft suitable for an etching apparatus having a reduced weight, in addition to being excellent in chemical resistance and being able to transport smoothly.

本発明者らは、上記の問題点を解決するために鋭意検討を進めた結果、耐薬品性、軽量性、成形収縮率に優れ、なおかつ低コストで製造が可能な搬送用シャフトを見出し、本発明を完成したものである。   As a result of diligent investigation to solve the above problems, the present inventors have found a transport shaft that is excellent in chemical resistance, light weight, molding shrinkage, and can be manufactured at low cost. The invention has been completed.

この搬送用シャフトの基材に用いるガラス糸を、耐薬品性が劣るE−ガラスに代えて高ジルコニア含有ガラス糸とし、また、樹脂にビニルエステルや不飽和ポリエステル樹脂、低収縮剤にポリエチレンを使用することで、耐薬品性、軽量性及び寸法安定性を満足し、搬送用シャフトとしての長期信頼性を満足することができ、さらに低コストな引抜成形品として製造することができる搬送用シャフトを見出した。   The glass yarn used for the substrate of this conveying shaft is replaced with E-glass with poor chemical resistance and glass yarn containing high zirconia, and vinyl ester or unsaturated polyester resin is used as the resin, and polyethylene is used as the low shrinkage agent. Therefore, a transport shaft that satisfies chemical resistance, light weight and dimensional stability, can satisfy long-term reliability as a transport shaft, and can be manufactured as a low-cost pultruded product. I found it.

すなわち、本発明の搬送用シャフトは、複数本のガラス繊維から収束されたガラス糸に熱硬化性樹脂組成物を含浸させ、引抜成形して得られる搬送用シャフトであって、ガラス繊維が、SiO 54〜65質量%、ZrO 14〜25質量%、NaO 10〜17質量%を必須成分として含有してなることを特徴とするものである。 That is, the conveyance shaft of the present invention is a conveyance shaft obtained by impregnating a glass yarn converged from a plurality of glass fibers with a thermosetting resin composition and pultrusion molding. 2 54-65 mass%, ZrO 2 14 to 25 wt% and is characterized by containing as an essential component Na 2 O 10 to 17 wt%.

本発明の搬送用シャフトによれば、耐薬品性、軽量性、成形収縮率に優れた引抜成形品として製造することができるため、製品の長期信頼性を高めることができ、かつ、特殊で高価なカーボン繊維を使用することなく製造することができるため、低コストで高信頼性の製品を提供することができる。   According to the conveying shaft of the present invention, since it can be manufactured as a pultruded product having excellent chemical resistance, light weight, and molding shrinkage, the long-term reliability of the product can be improved, and it is special and expensive. Therefore, it is possible to provide a highly reliable product at a low cost.

以下、本発明について詳細に説明する。   Hereinafter, the present invention will be described in detail.

本発明の搬送用シャフトは、基材として特定のガラス繊維を用い、このガラス繊維を収束して得られたガラス糸に熱硬化性樹脂組成物を含浸させて、これを引抜成形により成形し製品とするものである。   The conveying shaft of the present invention uses a specific glass fiber as a base material, impregnates the glass fiber obtained by converging the glass fiber with a thermosetting resin composition, and molds this by pultrusion molding. It is what.

ここで、本発明に用いる熱硬化性樹脂組成物は、ビニルエステル樹脂、不飽和ポリエステル樹脂等の熱硬化性樹脂をベース樹脂として用いることができ、ビニルエステル樹脂であることが好ましい。   Here, the thermosetting resin composition used in the present invention can use a thermosetting resin such as a vinyl ester resin or an unsaturated polyester resin as a base resin, and is preferably a vinyl ester resin.

この熱硬化性樹脂組成物としては、例えば、(A)ビニルエステル樹脂と、(B)架橋剤と、(C)低収縮剤と、(D)無機充填材と、(E)離型剤と、(F)有機過酸化物と、を必須成分として含有するものが挙げられる。   Examples of the thermosetting resin composition include (A) a vinyl ester resin, (B) a crosslinking agent, (C) a low shrinkage agent, (D) an inorganic filler, and (E) a release agent. And (F) an organic peroxide as an essential component.

本発明に用いる(A)ビニルエステル樹脂は、成形材料として一般に使用されているものであれば特に限定されずに使用することができ、例えば、D−953(大日本インキ工業株式会社製、商品名)等が挙げられる。このような(A)ビニルエステル樹脂は、(a)酸性分と(b)エポキシ樹脂成分を反応させて得られるものである。   The (A) vinyl ester resin used in the present invention can be used without particular limitation as long as it is generally used as a molding material. For example, D-953 (Dainippon Ink Industries, Ltd., product) Name). Such (A) vinyl ester resin is obtained by reacting (a) an acidic component and (b) an epoxy resin component.

ここで(a)酸成分としては、アクリル酸、メタクリル酸、クロトン酸、ソルビン酸等の不飽和一塩基酸が挙げられ、さらに必要に応じてフタル酸、無水フタル酸、イソフタル酸、テレフタル酸、テトラヒドロフタル酸、無水テトラヒドロフタル酸、ヘキサヒドロフタル酸、無水ヘキサヒドロフタル酸、アジピン酸等の二塩基酸を2種類以上混合して使用することもできる。   Here, examples of the acid component (a) include unsaturated monobasic acids such as acrylic acid, methacrylic acid, crotonic acid, and sorbic acid, and phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, A mixture of two or more dibasic acids such as tetrahydrophthalic acid, tetrahydrophthalic anhydride, hexahydrophthalic acid, hexahydrophthalic anhydride, and adipic acid can also be used.

また、(b)エポキシ樹脂成分としては、1分子中に2個以上のエポキシ基を有するものであれば、分子構造、分子量等に制限されることなく広く用いることができ、具体的には、ビスフェノール型、ノボラック型、ビフェニル型の芳香族基を有するエポキシ樹脂、ポリカルボン酸がグリシジルエーテル化したエポキシ樹脂、シクロヘキサン誘導体にエポキシ基が縮合した脂環式の基を有するエポキシ樹脂等が挙げられる。これらのエポキシ樹脂は、単独又は2種類以上を混合して使用することができる。さらに、エポキシ樹脂成分としては、これらの他に必要に応じて液状のモノエポキシ樹脂を併用成分として使用することができる。   In addition, as the (b) epoxy resin component, as long as it has two or more epoxy groups in one molecule, it can be widely used without being limited by molecular structure, molecular weight, etc. Specifically, Examples thereof include an epoxy resin having a bisphenol type, novolak type or biphenyl type aromatic group, an epoxy resin in which a polycarboxylic acid is glycidyl etherified, and an epoxy resin having an alicyclic group in which an epoxy group is condensed to a cyclohexane derivative. These epoxy resins can be used individually or in mixture of 2 or more types. Furthermore, as an epoxy resin component, in addition to these, a liquid monoepoxy resin can be used as a combined component as required.

この(A)ビニルエステル樹脂の配合量は、熱硬化性樹脂組成物中に70〜85質量%の範囲であることが好ましい。   It is preferable that the compounding quantity of this (A) vinyl ester resin is the range of 70-85 mass% in a thermosetting resin composition.

本発明に用いる(B)架橋剤としては、(A)ビニルエステル樹脂と重合可能な二重結合を有するものであれば使用可能であり、例えば、スチレンモノマー、ジビニルベンゼン、ジアリルフタレートモノマー、メタクリル酸メチル、トリアリルイソシアヌレート等が挙げられる。この(B)架橋剤の配合量は、熱硬化性樹脂組成物中に1〜2質量%の範囲であることが好ましい。   As the (B) cross-linking agent used in the present invention, any one having a double bond polymerizable with the (A) vinyl ester resin can be used. For example, styrene monomer, divinylbenzene, diallyl phthalate monomer, methacrylic acid Examples include methyl and triallyl isocyanurate. It is preferable that the compounding quantity of this (B) crosslinking agent is the range of 1-2 mass% in a thermosetting resin composition.

本発明に用いる(C)低収縮材としては、熱可塑性樹脂であるポリエチレン樹脂、飽和ポリエステル樹脂、ゴム、ポリエチレン等が使用可能であるが、耐薬品性、軽量性、低収縮性の観点からポリエチレン樹脂であることが好ましい。このうちガラス転移点が70〜120℃のポリエチレン樹脂粉末が耐薬品性及び成形収縮率の向上のために特に好ましい。この(C)低収縮材の配合量は、熱硬化性樹脂組成物中に0.5〜1.5質量%の範囲であることが好ましい。   As the (C) low shrinkage material used in the present invention, polyethylene resin, saturated polyester resin, rubber, polyethylene, etc., which are thermoplastic resins, can be used. From the viewpoint of chemical resistance, light weight, and low shrinkage, polyethylene is used. A resin is preferred. Among these, a polyethylene resin powder having a glass transition point of 70 to 120 ° C. is particularly preferable for improving chemical resistance and molding shrinkage. It is preferable that the compounding quantity of this (C) low shrinkage | contraction material is the range of 0.5-1.5 mass% in a thermosetting resin composition.

本発明に用いる(D)無機充填材としては、硫酸バリウム、炭酸カルシウム、水酸化アルミニウム、シリカ、ガラスバルーン等の通常用いられているものが挙げられ、特に限定されるものではない。この(D)無機充填材の配合量は、熱硬化性樹脂組成物中に10〜20質量%の範囲であることが好ましい。   Examples of the (D) inorganic filler used in the present invention include those usually used such as barium sulfate, calcium carbonate, aluminum hydroxide, silica, and glass balloon, and are not particularly limited. It is preferable that the compounding quantity of this (D) inorganic filler is the range of 10-20 mass% in a thermosetting resin composition.

本発明に用いる(E)離型剤は、成形材料として通常使用される離型剤であればよく、例えば、市販のシリコーンオイルが挙げられ、中でもエポキシ変性シリコーンオイルが好ましい。この(E)離型剤の配合量は熱硬化性樹脂組成物中に0.01〜2質量%である。   The (E) mold release agent used in the present invention may be any mold release agent that is usually used as a molding material. Examples thereof include commercially available silicone oils, and among these, epoxy-modified silicone oils are preferred. The compounding quantity of this (E) mold release agent is 0.01-2 mass% in a thermosetting resin composition.

本発明に用いる(F)有機過酸化物としては、ビニルエステル樹脂の硬化剤として通常用いられる化合物であれば、特に限定されるものではなく、例えば、過酸化ベンゾイル、過酸化ジ−t−ブチル、過酸化イソブチリル等が挙げられる。この(G)有機過酸化物の配合量は、熱硬化性樹脂組成物中に0.1〜2質量%の範囲であることが好ましい。   The organic peroxide (F) used in the present invention is not particularly limited as long as it is a compound that is usually used as a curing agent for vinyl ester resins, and examples thereof include benzoyl peroxide and di-t-butyl peroxide. And isobutyryl peroxide. It is preferable that the compounding quantity of this (G) organic peroxide is the range of 0.1-2 mass% in a thermosetting resin composition.

また、本発明に使用するガラス糸は、ガラス繊維を収束して得られた繊維基材であり、このガラス繊維は、SiO 54〜65質量%、ZrO 14〜25質量%、NaO 10〜17質量%を必須成分として含有し、その他の成分としては、LiO 0〜5質量%、KO 0〜8質量%、RO(ただし、Rは、Mg,Ca,Sr,Ba及びZnから選ばれる金属である。) 0〜10質量%、TiO 0〜7質量%、Al 0〜2質量%を含むものが挙げられる。このように特定の成分を所定量含む高ジルコニア含有ガラス繊維であれば、通常の製造条件で製造されたものでよい。 The glass yarn used in the present invention is a fibrous substrate obtained by converging glass fibers, the glass fibers are SiO 2 54 to 65 wt%, ZrO 2 14 to 25 wt%, Na 2 O It contains 10 to 17% by mass as essential components, and other components include Li 2 O 0 to 5% by mass, K 2 O 0 to 8% by mass, RO (where R is Mg, Ca, Sr, Ba) And 0 to 10% by mass, TiO 2 0 to 7% by mass, and Al 2 O 3 0 to 2% by mass. Thus, if it is a glass fiber containing high zirconia containing a specific amount of a specific component, it may be manufactured under normal manufacturing conditions.

ここで用いるガラス繊維は、表面にシランカップリング材によりサイジング処理を行い、耐薬品性を維持するようにすることが好ましく、このサイジング処理を行うサイジング剤としては、アルカリ成分との反応性が低く、マトリックス樹脂に対するぬれ性が良い薬剤が挙げられ、具体的には、メタクリルシランやウレイドシラン等のシランカップリング剤又はそれらの混合品であることが好ましい。   The glass fiber used here is preferably subjected to sizing treatment with a silane coupling material on the surface to maintain chemical resistance, and the sizing agent for performing this sizing treatment has low reactivity with an alkali component. Examples thereof include agents having good wettability with respect to the matrix resin. Specifically, a silane coupling agent such as methacryl silane or ureido silane or a mixture thereof is preferable.

繊維基材としては、上記のガラス繊維を必須とするが、その他に、E−ガラス繊維、T−ガラス繊維、D−ガラス繊維等のガラス繊維、カーボン繊維、耐薬品性の有機繊維等を併用して用いてもよい。   As a fiber base material, the above glass fiber is essential, but in addition, glass fiber such as E-glass fiber, T-glass fiber, D-glass fiber, carbon fiber, chemical-resistant organic fiber, etc. are used in combination. May be used.

この繊維基材の含有量は、成形品中の繊維基材の平均体積含有率(体積分率)で、50〜80%とすることが好ましい。50%未満であると成形品の剛性が乏しくなってしまい、80%を越えると繊維強化材に樹脂組成物が含浸していない部分ができ、引抜成形品の物性低下を引き起こしてしまう。引抜成形用の熱硬化性樹脂組成物と繊維基材との混合は、繊維糸に熱硬化性樹脂組成物を含浸させ、樹脂組成物が繊維基材に付着した状態とすることが好ましい。繊維基材が引抜成形時の引抜力に耐え得ることが必要であるので、繊維基材の構成を、繊維基材のロービングを引抜方向に配向させて使用することが好ましい。   The content of the fiber base material is preferably 50 to 80% in terms of the average volume content (volume fraction) of the fiber base material in the molded product. If it is less than 50%, the rigidity of the molded product becomes poor, and if it exceeds 80%, a portion where the fiber reinforcing material is not impregnated with the resin composition is formed, and the physical properties of the pultruded product are deteriorated. Mixing of the thermosetting resin composition for pultrusion and the fiber base material is preferably performed by impregnating the fiber yarn with the thermosetting resin composition so that the resin composition adheres to the fiber base material. Since it is necessary for the fiber base material to be able to withstand the drawing force at the time of pultrusion, it is preferable to use the fiber base material with the roving of the fiber base material oriented in the drawing direction.

そして、ここで用いる引抜成形方法は、上記したガラス繊維の複数本、例えば100〜500本のガラス繊維を収束して得られたガラス糸を熱硬化性樹脂組成物ワニスに含浸させ、このガラス繊維強化樹脂組成物を、加熱金型内を通すことによって熱硬化性樹脂組成物を硬化させ、金型形状により外形を整えて引抜き、成形品を形成するものである。この引抜成形においては、用いる樹脂組成物に応じて、加熱温度及び引抜速度を適宜選択して行うことができる。   And the pultrusion method used here impregnates the thermosetting resin composition varnish with a glass yarn obtained by converging a plurality of glass fibers described above, for example, 100 to 500 glass fibers, and this glass fiber. By passing the reinforced resin composition through a heating mold, the thermosetting resin composition is cured, the outer shape is adjusted according to the shape of the mold, and the molded article is formed. This pultrusion molding can be performed by appropriately selecting the heating temperature and the drawing speed according to the resin composition to be used.

ここで、ガラス繊維強化樹脂組成物が付される金型温度は、100〜200℃程度であることが好ましい。100℃未満であると、ガラス繊維強化樹脂組成物の未硬化の状態で引き抜かれ易くなってしまい、200℃を越えると、硬化反応が急激に起こるため成形品にクラックやそり等の不良を生じさせる可能性が高くなる。   Here, the mold temperature to which the glass fiber reinforced resin composition is attached is preferably about 100 to 200 ° C. If the temperature is lower than 100 ° C, the glass fiber reinforced resin composition is easily pulled out in an uncured state. If the temperature exceeds 200 ° C, the curing reaction occurs rapidly, so that defects such as cracks and warpage occur in the molded product. The possibility of making it high.

また、引抜速度は10〜120cm/分であることが好ましい。引抜速度が10cm/分未満であると、成形型中での硬化が早い時点で完了してしまい、引き抜く際の抵抗が大きくなり安定的に連続成形できなくなってしまい、一方、引抜速度が120cm/分を越えると、ガラス繊維強化樹脂組成物が未硬化の状態で引き抜かれ易くなってしまう。したがって、引抜時間(金型中を通過する時間)は0.5〜3.0分の範囲内となることが好ましい。   The drawing speed is preferably 10 to 120 cm / min. When the drawing speed is less than 10 cm / min, the curing in the mold is completed at an early stage, and the resistance at the time of drawing becomes large and stable continuous molding becomes impossible. On the other hand, the drawing speed is 120 cm / min. When it exceeds the minute, the glass fiber reinforced resin composition is easily pulled out in an uncured state. Therefore, the drawing time (time for passing through the mold) is preferably in the range of 0.5 to 3.0 minutes.

すなわち、引抜成形では、ガラス繊維強化樹脂組成物を、加熱された金型内に連続的に引き込み、金型内通過中に樹脂を所定の温度に付して硬化させると共に、金型出口から所定の時間で引き抜くのである。この引抜成形方法で用いられる装置は、通常用いられている引抜成形装置であれば、特に限定されずに使用することができる。   That is, in pultrusion molding, the glass fiber reinforced resin composition is continuously drawn into a heated mold, and the resin is subjected to a predetermined temperature and cured while passing through the mold, and at the same time from the mold outlet. It will be pulled out in the time. The apparatus used in this pultrusion method is not particularly limited as long as it is a commonly used pultrusion apparatus.

金型はヒーター等で加熱制御されており、金型の入口と金型の他の部分の温度を別々に制御してもよく、例えば、金型の入口温度は、入口で絞られる繊維強化樹脂組成物のゲル化を抑制する観点から、使用する硬化剤の反応温度より低く抑え、金型の他の部分の温度は、ガラス繊維強化樹脂組成物を硬化させる観点から、使用する硬化剤の作用温度以上にすることが好ましい。このように加熱帯を2段階やそれ以上に分割することで、入口付近のゲル化を抑制しつつ、後の加熱でガラス繊維強化樹脂組成物を効率的に硬化させることができ、操作性良く成形することができる。   The mold is heated and controlled by a heater or the like, and the temperature of the mold inlet and the other part of the mold may be controlled separately. For example, the mold inlet temperature is a fiber reinforced resin squeezed at the inlet From the viewpoint of suppressing the gelation of the composition, the temperature of the other part of the mold is suppressed to be lower than the reaction temperature of the curing agent to be used, and from the viewpoint of curing the glass fiber reinforced resin composition, It is preferable to set the temperature or higher. Thus, by dividing the heating zone into two steps or more, the glass fiber reinforced resin composition can be efficiently cured by subsequent heating while suppressing gelation in the vicinity of the inlet, with good operability. Can be molded.

このようにして得られた成形品は、低収縮剤を混合することにより、体積収縮が小さく、外観及び物性にも優れた成形品とすることができる。   The molded product thus obtained can be made into a molded product having a small volume shrinkage and excellent appearance and physical properties by mixing a low shrinkage agent.

以下、本発明を実施例により具体的に説明する。   Hereinafter, the present invention will be specifically described by way of examples.

(実施例1)
熱硬化性樹脂成分として、ビニルエステル(大日本インキ工業株式会社製、商品名:UE3505) 22質量部、スチレンモノマー(日本ユピカ株式会社製、商品名:スチレンモノマー) 0.35質量部、ポリエチレン(住友精化株式会社製、商品名:フローセンUF−1.5) 0.25質量部、硫酸バリウム(堺化学工業株式会社製、商品名:沈降性硫酸バリウム−100) 3.7質量部、有機過酸化物1(日本油脂株式会社製、商品名:パーブチルO) 0.06質量部、有機過酸化物2(日本油脂株式会社、商品名:パーヘキサHC) 0.35質量部、離型材(小桜商会株式会社、商品名:INT−1850HT〔有機酸、グリセリド、合成樹脂縮合体〕) 0.35質量部を混練機(ニーダー)にいれ、約20分間混練し、熱硬化性成形材料を得た。なお、配合量は熱硬化性成形材料の構成成分全量に対するそれぞれの配合量を示したものである。
Example 1
As a thermosetting resin component, 22 parts by mass of vinyl ester (manufactured by Dainippon Ink Industries, Ltd., trade name: UE3505), 0.35 parts by mass of styrene monomer (manufactured by Nippon Yupica, trade name: styrene monomer), polyethylene Sumitomo Seika Chemicals Co., Ltd., trade name: Frocene UF-1.5) 0.25 parts by mass, barium sulfate (manufactured by Sakai Chemical Industry Co., Ltd., trade name: precipitated barium sulfate-100) 3.7 parts by mass, organic Peroxide 1 (Nippon Yushi Co., Ltd., trade name: Perbutyl O) 0.06 parts by mass, Organic peroxide 2 (Nippon Yushi Co., Ltd., trade name: Perhexa HC) 0.35 parts by mass, release material (Kosakura) Shokai Co., Ltd., trade name: INT-1850HT [Organic acid, glyceride, synthetic resin condensate]) 0.35 parts by mass is put into a kneader (kneader), kneaded for about 20 minutes, and thermosetting. A molding material was obtained. In addition, the compounding quantity shows each compounding quantity with respect to the component total quantity of a thermosetting molding material.

次に、基材としてガラス糸 ARG(日本電気硝子株式会社製、商品名:AR1500−800/DB)を、得られた熱硬化性成形材料の入った樹脂槽に含浸させ、樹脂を含浸させたガラス糸を約165℃の加熱金型(長さ:600〜800mm)に送り込み加熱硬化を行い、20〜30cm/分のスピードで引抜いて丸棒を得て切断装置で切断し、ガラス繊維の体積分率が73%の成形品を得た。
得られた引抜成形品を8mmφに機械加工し搬送用シャフトを製造した。
Next, glass yarn ARG (trade name: AR1500-800 / DB, manufactured by Nippon Electric Glass Co., Ltd.) was impregnated into the resin tank containing the obtained thermosetting molding material as a base material, and the resin was impregnated. The glass yarn is fed into a heating mold (length: 600 to 800 mm) at about 165 ° C., heat-cured, drawn at a speed of 20 to 30 cm / min to obtain a round bar and cut with a cutting device, and the volume of the glass fiber. A molded product having a fraction of 73% was obtained.
The obtained pultruded product was machined to 8 mmφ to produce a conveying shaft.

(実施例2、比較例1〜2)
実施例1と同様の操作により、表2に示した配合量に従い、搬送用シャフトを製造した。なお、ここで、不飽和ポリエステルとしてはユピカ3464(日本ユピカ株式会社製、商品名)を、E−ガラスとしてはERS2310−554A/L(セントラル硝子株式会社製、商品名)を、それぞれ用いた。
(Example 2, Comparative Examples 1-2)
According to the same operation as in Example 1, a conveying shaft was produced according to the blending amount shown in Table 2. Here, as the unsaturated polyester, Iupica 3464 (manufactured by Nippon Iupika Co., Ltd., trade name) was used, and as the E-glass, ERS2310-554A / L (manufactured by Central Glass Co., Ltd., trade name) was used.

Figure 0004850551
Figure 0004850551

Figure 0004850551
Figure 0004850551

*1:JIS K 6911に準じて測定した。
*2:JIS K 6911に準じて測定した。
*3:JIS K 6911に準じて測定した。
*4:JIS K 6911に準じて測定した。
*5:試験片を、塩化第2銅+3N塩酸水溶液(80℃)に浸漬し、1000時間処理した時の処理前後の重量変化率を測定した。
*6:試験片を、3%苛性ソーダ水溶液(80℃)に浸漬し、1000時間処理した時の処理前後の重量変化率を測定した。
* 1: Measured according to JIS K 6911.
* 2: Measured according to JIS K 6911.
* 3: Measured according to JIS K 6911.
* 4: Measured according to JIS K 6911.
* 5: The weight change rate before and after the treatment was measured when the test piece was immersed in cupric chloride + 3N hydrochloric acid aqueous solution (80 ° C.) and treated for 1000 hours.
* 6: The weight change rate before and after the treatment when the test piece was immersed in a 3% aqueous sodium hydroxide solution (80 ° C.) and treated for 1000 hours was measured.

なお、*5、*6の判定は、重量変化率の数値範囲に基づき、次の基準により行った。
◎:0〜0.20%
○:0.21〜0.50%
△:0.51〜1.00%
×:1.00%以上
Note that * 5 and * 6 were determined based on the following criteria based on the numerical range of the weight change rate.
A: 0 to 0.20%
○: 0.21 to 0.50%
Δ: 0.51 to 1.00%
X: 1.00% or more

Claims (3)

複数本のガラス糸に熱硬化性樹脂組成物を含浸させ、引抜成形して得られる搬送用シャフトであって、
前記ガラス糸を構成するガラス繊維基材が、SiO 54〜65質量%、ZrO 14〜25質量%、NaO 10〜17質量%を必須成分として含有してなり、
前記熱硬化性樹脂組成物が、(A)ビニルエステル樹脂と、(B)架橋剤と、(C)低収縮剤と、(D)無機充填材と、(E)離型剤と、(F)有機過酸化物と、を必須成分とするエッチング装置用搬送用シャフト。
A shaft for conveyance obtained by impregnating a plurality of glass yarns with a thermosetting resin composition and pultrusion molding,
Glass fiber base material constituting the glass yarns, SiO 2 54 to 65 wt%, ZrO 2 14 to 25 wt%, Ri Na contained as Na 2 O 10 to 17 wt% of the essential components,
The thermosetting resin composition comprises (A) a vinyl ester resin, (B) a crosslinking agent, (C) a low shrinkage agent, (D) an inorganic filler, (E) a release agent, and (F ) A transport shaft for an etching apparatus which contains an organic peroxide as an essential component .
前記ガラス繊維が、シランカップリング剤でサイジング処理されてなることを特徴とする請求項1記載のエッチング装置用搬送用シャフト。 2. The transport shaft for an etching apparatus according to claim 1, wherein the glass fiber is sizing treated with a silane coupling agent. 前記(C)低収縮材として、70〜120℃のガラス転移点を有するポリエチレンを熱硬化性樹脂組成物中に0.5〜1.5質量%用いることを特徴とする請求項1又は2記載のエッチング装置用搬送用シャフト。 Examples (C) low shrinkage material, according to claim 1, wherein the use 0.5 to 1.5 wt% of polyethylene a thermosetting resin composition having a glass transition point of 70 to 120 ° C. Conveyor shaft for etching equipment .
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