JP5624423B2 - Prepreg tape roll - Google Patents
Prepreg tape roll Download PDFInfo
- Publication number
- JP5624423B2 JP5624423B2 JP2010228966A JP2010228966A JP5624423B2 JP 5624423 B2 JP5624423 B2 JP 5624423B2 JP 2010228966 A JP2010228966 A JP 2010228966A JP 2010228966 A JP2010228966 A JP 2010228966A JP 5624423 B2 JP5624423 B2 JP 5624423B2
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- JP
- Japan
- Prior art keywords
- prepreg
- film
- tape
- prepreg tape
- photocurable
- Prior art date
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- 239000002131 composite material Substances 0.000 claims description 75
- 238000004804 winding Methods 0.000 claims description 24
- 239000011342 resin composition Substances 0.000 claims description 21
- -1 polyethylene terephthalate Polymers 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 9
- 230000002093 peripheral effect Effects 0.000 claims description 9
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 8
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229920006284 nylon film Polymers 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- 229920005992 thermoplastic resin Polymers 0.000 claims description 4
- 239000004925 Acrylic resin Substances 0.000 claims description 3
- 239000003349 gelling agent Substances 0.000 claims description 3
- 239000003365 glass fiber Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 description 22
- 239000011347 resin Substances 0.000 description 22
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 9
- 230000001070 adhesive effect Effects 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 239000003999 initiator Substances 0.000 description 8
- 229920006337 unsaturated polyester resin Polymers 0.000 description 6
- 230000008719 thickening Effects 0.000 description 5
- 150000007519 polyprotic acids Polymers 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 238000010276 construction Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 238000010526 radical polymerization reaction Methods 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000012783 reinforcing fiber Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 229920006305 unsaturated polyester Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- FQKYTBQZPFRTDH-UHFFFAOYSA-N 2-hydroxy-1-phenylbutan-1-one Chemical compound CCC(O)C(=O)C1=CC=CC=C1 FQKYTBQZPFRTDH-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/02—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments
- B32B17/04—Layered products essentially comprising sheet glass, or glass, slag, or like fibres in the form of fibres or filaments bonded with or embedded in a plastic substance
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/06—Interconnection of layers permitting easy separation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Reinforced Plastic Materials (AREA)
- Laminated Bodies (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
Description
本発明は、光硬化性プリプレグテープに剥離性フィルムを貼付してなるプリプレグ複合テープを巻回状態にしたプリプレグテープ巻回体に関する。 The present invention relates to a prepreg tape wound body in which a prepreg composite tape formed by attaching a peelable film to a photocurable prepreg tape is wound.
従来、配管物や各種構造部材などの補修、補強、あるいは防水用ライニング材等として使用される光硬化性プリプレグテープは、不飽和ポリエステル樹脂などの重合性樹脂に光重合開始剤、増粘剤等を配合してなる光硬化性樹脂組成物をガラスクロスや不織布等の基材に含浸、増粘してつくられている。
また、この光硬化性プリプレグテープ(以下、単にプリプレグテープとも言う)は、図6に示すように、その両面に剥離性のフィルム120を貼着させた複合テープ130の状態とし、樹脂成分を未硬化の状態で保管される。フィルム120としては、透明なプラスチックフィルム等の、光透過性(特に、プリプレグテープの硬化波長の光透過性が充分に確保されているもの)の樹脂フィルムを用いることが一般的である。
Conventionally, photocurable prepreg tapes used for repairing, reinforcing, waterproofing lining materials, etc. for pipes and various structural members are photopolymerization initiators, thickeners, etc. for polymerizable resins such as unsaturated polyester resins. It is made by impregnating a substrate such as a glass cloth or a non-woven fabric with a photocurable resin composition obtained by blending and thickening.
Further, as shown in FIG. 6, this photo-curable prepreg tape (hereinafter also simply referred to as a prepreg tape) is in a state of a composite tape 130 having a peelable film 120 attached on both sides thereof, and the resin component is not yet present. Stored in a cured state. As the film 120, it is common to use a resin film such as a transparent plastic film, which is light transmissive (particularly, a film having sufficient light transmittance at the curing wavelength of the prepreg tape).
複合テープ130のプリプレグテープ110を被着物に接着する作業の代表的手順としては、以下のものがある。まず、プリプレグテープ110の両面のフィルム120の片方(以下、第1フィルム121とも言う)をプリプレグテープ110から引き剥がし、この第1フィルム121の引き剥がしによって露出させたプリプレグテープ110の片面を被着物に圧接、粘着させる。次いで、この状態で、プリプレグテープ110に該プリプレグテープ110に被着状態のままのフィルム120(以下、第2フィルム122とも言う表面側フィルムとも言う)を介して光(プリプレグテープ110の樹脂成分を硬化させる波長を含む光)を照射し、プリプレグテープ110の樹脂成分を硬化させた後、表面側フィルムをプリプレグテープ110から引き剥がす。
第2フィルム122は、光照射によって硬化したプリプレグテープ110が粘着力を喪失することで、プリプレグテープ110からの引き剥がしを弱い力で楽に行える。
As typical procedures for bonding the prepreg tape 110 of the composite tape 130 to the adherend, there are the following procedures. First, one side of the film 120 on both sides of the prepreg tape 110 (hereinafter also referred to as the first film 121) is peeled off from the prepreg tape 110, and one side of the prepreg tape 110 exposed by peeling off the first film 121 is attached. Press and stick to. Next, in this state, the light (the resin component of the prepreg tape 110 is applied to the prepreg tape 110 via a film 120 (hereinafter also referred to as a second film 122) that is still attached to the prepreg tape 110. After the resin component of the prepreg tape 110 is cured, the surface side film is peeled off from the prepreg tape 110.
The second film 122 can be easily peeled off from the prepreg tape 110 with a weak force when the prepreg tape 110 cured by light irradiation loses the adhesive force.
なお、第1フィルム121は、プリプレグテープ110に接する面のみにシリコーン処理が施されており、未硬化のプリプレグテープ110から容易に剥離させることができる。一方、第2フィルム122は、未硬化のプリプレグテープ110からの剥離性を確保するための処理(シリコーン処理等)は施されておらず、未硬化のプリプレグテープ110に対する密着性が確保される。この第2フィルム122は、光照射によるプリプレグテープ110の硬化まで、プリプレグテープ110の粘着力によってプリプレグテープ110に貼着した状態が保たれる。 The first film 121 is subjected to silicone treatment only on the surface in contact with the prepreg tape 110 and can be easily peeled off from the uncured prepreg tape 110. On the other hand, the second film 122 is not subjected to a treatment (silicone treatment or the like) for ensuring the peelability from the uncured prepreg tape 110, and the adhesion to the uncured prepreg tape 110 is secured. The second film 122 is kept attached to the prepreg tape 110 by the adhesive force of the prepreg tape 110 until the prepreg tape 110 is cured by light irradiation.
ところで、前記複合テープ130の保管は、プリプレグテープの樹脂成分の未硬化状態を維持するため、遮光性を確保する必要がある。長尺の複合テープは、巻回状態にして、遮光性の袋等の遮光性収納容器に入れて保管することが一般的である。前記複合テープ130は、巻回状態(巻回体)にしたときに、プリプレグテープ110の両面のフィルム120がプリプレグテープ110同士の直接接触、粘着を防ぐ機能を果たすため、巻回体からの引き出し作業を楽に行える。
しかしながら、図7に示すように、従来構成の複合テープ130は、巻回状態にして保管したとき、巻回による該複合テープ130の内周側のフィルムと外周側のフィルムとの周長差によって巻き皺が発生することがあった。複合テープ130の巻き皺は、プリプレグテープ110の被着物に対する接着時の密着作業性に影響を与えることがあるため、この発生を防止したいという要求がある。
By the way, storage of the composite tape 130 needs to ensure light shielding properties in order to maintain the uncured state of the resin component of the prepreg tape. In general, long composite tapes are wound and stored in a light-shielding container such as a light-shielding bag. When the composite tape 130 is wound (wound body), the films 120 on both sides of the prepreg tape 110 serve to prevent direct contact and adhesion between the prepreg tapes 110. Work can be done easily.
However, as shown in FIG. 7, when the composite tape 130 having the conventional configuration is stored in a wound state, the composite tape 130 is wound due to a difference in peripheral length between the inner peripheral film and the outer peripheral film of the composite tape 130. A curl may occur. Since the curl of the composite tape 130 may affect the workability of adhesion when the prepreg tape 110 is adhered to the adherend, there is a demand for preventing this occurrence.
特許文献1には、硬化性のプリプレグの製造工程における皺発生を防止するために、樹脂がBステージ(半硬化)に至るまで加熱乾燥したプリプレグを、樹脂粘度が最も低くなる温度よりも20〜40℃低い温度に加熱する技術が開示されている。
しかしながら、特許文献1に開示された技術は、加熱乾燥後のプリプレグを再加熱によって軟化させることで、ロール通過時の皺発生を防止するものであり、巻回状態にしたときの巻き皺の発生を防止できるものではない。
In Patent Document 1, in order to prevent generation of wrinkles in the production process of a curable prepreg, a prepreg heated and dried until the resin reaches a B stage (semi-cured) is 20 to 20 ° C. lower than the temperature at which the resin viscosity is lowest. A technique for heating to a temperature lower by 40 ° C. is disclosed.
However, the technique disclosed in Patent Document 1 is to soften the prepreg after heat drying by reheating, thereby preventing wrinkle generation when passing through the roll. It can not prevent.
複合テープ130の巻回体の作製にあたって巻き皺の発生を防止できる適切な技術は、現状、存在しないのが実情である。
本発明は、上述の事情に鑑み、巻回状態にしたときの巻き皺の発生を防止できるプリプレグテープ巻回体を提供することを目的とする。
In actuality, there is currently no suitable technique capable of preventing the occurrence of curling in the production of the wound body of the composite tape 130.
An object of this invention is to provide the prepreg tape winding body which can prevent generation | occurrence | production of a winding fist when it makes a winding state in view of the above-mentioned situation.
上記課題を解決するために、本発明では以下の構成を提供する。
本発明は、プリプレグ複合テープを巻回してなるプリプレグテープ巻回体であって、前記プリプレグ複合テープは、光硬化性プリプレグテープの片面のみに、光透過性を有する剥離性のフィルムが貼着され、前記光硬化性プリプレグテープは、液状の光硬化性樹脂組成物をガラス繊維からなる基材に含浸させて構成され、前記光硬化性樹脂組成物はエポキシアクリレート樹脂からなり、熱可塑性樹脂粒子をゲル化剤として配合して増粘され、前記フィルムは、前記光硬化性プリプレグテープに接する貼着面とは反対の表面側にのみシリコーン処理が施されているプリプレグテープ巻回体を提供する。
前記フィルムは、前記光硬化性プリプレグテープの外周側に貼着されていることが好ましい。
前記プリプレグ複合テープのフィルムは、ポリエチレンテレフタレートフィルム、ポリエチレンフィルム、ポリプロピレンフィルム、ポリ塩化ビニルフィルム、ナイロンフィルムのいずれか1つであることが好ましい。
In order to solve the above problems, the present invention provides the following configuration.
The present invention is a prepreg tape wound body obtained by winding a prepreg composite tape, and the prepreg composite tape has a light-peelable peelable film attached to only one side of the photocurable prepreg tape. The photocurable prepreg tape is constituted by impregnating a substrate made of glass fiber with a liquid photocurable resin composition, and the photocurable resin composition is made of an epoxy acrylate resin, and includes thermoplastic resin particles. The film is blended as a gelling agent and thickened, and the film provides a prepreg tape wound body in which silicone treatment is performed only on the surface opposite to the sticking surface in contact with the photocurable prepreg tape.
The film is preferably attached to the outer peripheral side of the photocurable prepreg tape .
The film of the prepreg composite tape is preferably a polyethylene terephthalate film, a polyethylene film, a polypropylene film, a polyvinyl chloride film, or a nylon film.
本発明によれば、プリプレグ複合テープを巻回状態にしたときの巻き皺の発生を防止できる。
また、本発明によれば、光硬化性プリプレグテープの片面のみにフィルムを貼付した構成であるため、プリプレグテープの両面にフィルムが貼付された従来構成の複合テープに比べて低コスト化を容易に実現できる。しかも、本発明は、プリプレグ複合テープを巻回状態にした巻回体の、プリプレグテープの長さに対する巻き径縮小も容易に実現できる。
According to the present invention, it is possible to prevent the occurrence of curl when the prepreg composite tape is wound.
In addition, according to the present invention, since the film is attached to only one side of the photocurable prepreg tape, the cost can be easily reduced as compared with the composite tape having the conventional structure in which the film is attached to both sides of the prepreg tape. realizable. And this invention can also implement | achieve easily the winding diameter reduction with respect to the length of a prepreg tape of the winding body which made the prepreg composite tape the winding state.
以下、本発明の1実施形態を図面を参照して説明する。
図1、図2に示すように、ここで説明するプリプレグ複合テープ10は、液状の光硬化性樹脂組成物をガラスクロスや不織布等の基材(図示略)に含浸、増粘してなる光硬化性プリプレグテープ11(以下、単にプリプレグテープとも言う)の片面のみに、剥離性のフィルム12を貼着(貼付)した概略構成になっている。
Hereinafter, an embodiment of the present invention will be described with reference to the drawings.
As shown in FIGS. 1 and 2, the prepreg composite tape 10 described here is a light obtained by impregnating and thickening a base material (not shown) such as a glass cloth or a nonwoven fabric with a liquid photocurable resin composition. It has a schematic configuration in which a peelable film 12 is attached (attached) only to one side of a curable prepreg tape 11 (hereinafter also simply referred to as a prepreg tape).
このプリプレグ複合テープ10のプリプレグテープ11の光硬化性樹脂組成物は、例えば不飽和ポリエステル樹脂といった重合性樹脂に光重合開始剤、増粘剤等を配合したものである。
このプリプレグ複合テープ10において、プリプレグテープ11の光硬化性樹脂組成物は、未硬化状態になっている。また、プリプレグテープ11及びプリプレグ複合テープ10は、光硬化性樹脂組成物が未硬化状態であるとき高い柔軟性を有し、プリプレグテープ11を被着(接着)固定する被着物の表面形状に対する追従性に優れ、被着物表面に対する密着性を容易に確保できる。
The photocurable resin composition of the prepreg tape 11 of the prepreg composite tape 10 is obtained by blending a photopolymerization initiator, a thickener, and the like with a polymerizable resin such as an unsaturated polyester resin.
In this prepreg composite tape 10, the photocurable resin composition of the prepreg tape 11 is in an uncured state. The prepreg tape 11 and the prepreg composite tape 10 have high flexibility when the photocurable resin composition is in an uncured state, and follow the surface shape of the adherend that adheres (adheres) and fixes the prepreg tape 11. It can be easily secured and adherence to the adherend surface.
光硬化性樹脂組成物は、光照射によって硬化する性質を持つものである。この光硬化性樹脂組成物としては、例えば紫外線の照射によって硬化する周知のものを採用できる。また、光硬化性樹脂組成物としては、赤外線の照射によって硬化するもの、可視光の照射によって硬化するものも採用可能である。 The photocurable resin composition has a property of being cured by light irradiation. As this photocurable resin composition, for example, a well-known one that is cured by irradiation with ultraviolet rays can be employed. Moreover, as a photocurable resin composition, what hardens | cures by irradiation of infrared rays and what hardens | cures by irradiation of visible light are also employable.
光硬化性樹脂組成物の重合性樹脂としては、ラジカル重合可能な不飽和ポリエステル樹脂及びカチオン重合可能なエポキシ樹脂が代表的に挙げられるが、安定した増粘体が得やすい、取扱い易いという理由でラジカル重合性樹脂が好適に使用される。
ラジカル重合性樹脂とは、ラジカル重合可能な二重結合性不飽和基を有する化合物を液状ビニル系単量体に溶解した液状樹脂である。
ラジカル重合可能な液状樹脂としては、不飽和ポリエステル樹脂をはじめ、エポキシアクリレート樹脂、ウレタンアクリレート樹脂、アリルエステル樹脂等がその例である。
Typical examples of the polymerizable resin of the photocurable resin composition include an unsaturated polyester resin capable of radical polymerization and an epoxy resin capable of cationic polymerization. However, radicals are preferred because a stable thickener is easily obtained and easy to handle. A polymerizable resin is preferably used.
The radical polymerizable resin is a liquid resin in which a compound having a double bondable unsaturated group capable of radical polymerization is dissolved in a liquid vinyl monomer.
Examples of liquid resins capable of radical polymerization include unsaturated polyester resins, epoxy acrylate resins, urethane acrylate resins, and allyl ester resins.
ラジカル重合可能な液状樹脂として使用される不飽和ポリエステル樹脂とは、多価アルコールと不飽和多塩基酸(および必要に応じて飽和多塩基酸)とのエステル化反応による縮合生成物(不飽和ポリエステル)を、スチレンのような液状ビニル系単量体に溶解したものである。 The unsaturated polyester resin used as a radically polymerizable liquid resin is a condensation product (unsaturated polyester) obtained by an esterification reaction between a polyhydric alcohol and an unsaturated polybasic acid (and a saturated polybasic acid if necessary). ) Is dissolved in a liquid vinyl monomer such as styrene.
ラジカル重合成樹脂に用いられる光重合開始剤としては、光照射によってラジカルを生成し、ラジカル重合可能な液状樹脂を重合、架橋して、組成物全体を硬化させるものを用いる。光照射によってラジカルを発生する重合開始剤としては、アセトフェノン系、ベンゾフェノン系、アシルホスフィンオキサイド系のような公知の光重合開始剤が挙げられ、具体例としては、2,4,6−トリメチルベンゾイルジフェニルホスフィンオキサイド、1−フェニル−2−ヒドロキシ−3−メチルプロパン−1−オン、1−ヒドロキシシクロヘキシルフェニルケトン、2−ヒドロキシ−2−メチル−1−フェニルプロパン−1−オン等が挙げられる。
これら重合開始剤は、その1種を用いてもよいし、2種以上を組み合わせて用いてもよい。
As the photopolymerization initiator used for the radical polysynthetic resin, one that generates radicals by light irradiation, polymerizes and crosslinks a radically polymerizable liquid resin, and cures the entire composition is used. Examples of polymerization initiators that generate radicals upon irradiation with light include known photopolymerization initiators such as acetophenone, benzophenone, and acylphosphine oxides. Specific examples include 2,4,6-trimethylbenzoyldiphenyl. Examples include phosphine oxide, 1-phenyl-2-hydroxy-3-methylpropan-1-one, 1-hydroxycyclohexyl phenyl ketone, and 2-hydroxy-2-methyl-1-phenylpropan-1-one.
One of these polymerization initiators may be used, or two or more thereof may be used in combination.
ラジカル重合性樹脂組成物を増粘する方法としては、例えば熱可塑性樹脂粒子をゲル化剤として配合してゼリー状に増粘させる方法、ヒドロキシル基を有するアクリレート樹脂をイソシアネート化合物で増粘させる方法等周知の方法が使用できる。増粘剤として使用される熱可塑性樹脂粒子としては、アクリル酸エステル、メタクリル酸エステル、芳香族ビニル化合物などを単量体とする重合体および共重合体が用いられる。 Examples of the method for thickening the radical polymerizable resin composition include a method of thickening a jelly resin by adding thermoplastic resin particles as a gelling agent and a method of thickening an acrylate resin having a hydroxyl group with an isocyanate compound. Well known methods can be used. As the thermoplastic resin particles used as the thickener, polymers and copolymers having acrylic acid ester, methacrylic acid ester, aromatic vinyl compound and the like as monomers are used.
プリプレグテープ11の基材としては、光硬化性樹脂組成物に含まれる光重合開始剤の感光波長域の光に対して実質的に透明の繊維によって構成されたもの(繊維基材)を好適に用いることができる。繊維基材の構成繊維(補強繊維)としては、光透過性及び強度の点で優れ、また低廉でもあるガラス繊維を好適に使用できる。繊維基材を構成する補強繊維としては、これ以外にもアラミド繊維、アクリル繊維、ポリエステル繊維、ポリエチレン繊維、ナイロン繊維等を使用することができる。使用する繊維は、一種を選択してもよいし、複数種を選択してもよい。
また、繊維基材の形態としては、例えば、チョップドストランドマット、ロービング、織物状などが挙げられる。
As a base material of the prepreg tape 11, a material (fiber base material) composed of fibers that are substantially transparent to light in the photosensitive wavelength region of the photopolymerization initiator contained in the photocurable resin composition is suitably used. Can be used. As the constituent fiber (reinforcing fiber) of the fiber base material, glass fiber which is excellent in terms of light transmittance and strength and is inexpensive can be suitably used. In addition to this, aramid fiber, acrylic fiber, polyester fiber, polyethylene fiber, nylon fiber, and the like can be used as the reinforcing fiber constituting the fiber base material. One type of fiber to be used may be selected, or a plurality of types may be selected.
Moreover, as a form of a fiber base material, a chopped strand mat, roving, a textile form etc. are mentioned, for example.
フィルム12としては、光硬化性樹脂組成物に含まれる光重合開始剤の感光波長域の光に対して実質的に透明のプラスチック製フィルムであり、ここではポリエチレンテレフタレート(PET)製のフィルムを用いている。但し、このフィルム12の材質としては、ポリエチレンテレフタレートに限定されず、例えば、ポリブチレンテレフタレート等も採用可能である。また、フィルム12としては、ポリエステルフィルム、ナイロンフィルム、ビニロンフィルム、ポリカーボネートフィルム、ポリエチレンフィルム、ポリプロピレンフィルム、ポリ塩化ビニルフィルム等も採用可能である。 The film 12 is a plastic film that is substantially transparent to light in the photosensitive wavelength range of the photopolymerization initiator contained in the photocurable resin composition. Here, a film made of polyethylene terephthalate (PET) is used. ing. However, the material of the film 12 is not limited to polyethylene terephthalate, and for example, polybutylene terephthalate can also be used. As the film 12, a polyester film, a nylon film, a vinylon film, a polycarbonate film, a polyethylene film, a polypropylene film, a polyvinyl chloride film, or the like can be used.
但し、フィルム12としては、伸びが小さい点で、ポリエチレンテレフタレートフィルムが好適である。また、フィルム12としては、ポリエチレンテレフタレートの延伸フィルムを特に好適に用いることができる。
ポリエステルフィルム、ナイロンフィルム、ポリプロピレンフィルムは、例えば光硬化性樹脂組成物の重合性樹脂として、多価アルコールと不飽和多塩基酸(および必要に応じて飽和多塩基酸)とのエステル化反応による縮合生成物(不飽和ポリエステル)をスチレンに溶解した不飽和ポリエステル樹脂のように、スチレンを含有するものを用いた場合に、スチレンの影響によって膨潤して、若干の伸びを生じ得る。これに対して、ポリエチレンテレフタレートフィルムは、スチレンに対する膨潤の影響を殆ど受けることがなく、寸法安定性の点で好適に用いることができる。
However, as the film 12, a polyethylene terephthalate film is suitable because it has a small elongation. Further, as the film 12, a stretched film of polyethylene terephthalate can be used particularly preferably.
Polyester film, nylon film, and polypropylene film, for example, as a polymerizable resin for a photocurable resin composition, are condensed by an esterification reaction between a polyhydric alcohol and an unsaturated polybasic acid (and a saturated polybasic acid if necessary). When a product containing styrene such as an unsaturated polyester resin in which a product (unsaturated polyester) is dissolved in styrene is used, it may swell under the influence of styrene and cause a slight elongation. On the other hand, the polyethylene terephthalate film is hardly affected by swelling with respect to styrene, and can be suitably used in terms of dimensional stability.
プリプレグ複合テープ10において、前記フィルム12は、未硬化状態のプリプレグテープ11の粘着力によってプリプレグテープ11に貼着されている。
このフィルム12のプリプレグテープ11とは反対側の面(以下、表面12a)には、シリコ−ン処理が施されている。フィルム12はその表面12a全体がシリコーン処理された面となっている。フィルム12は、その表面12aに未硬化状態のプリプレグテープ11が接触してもプリプレグテープ11が容易に粘着せず、粘着しても簡単に引き剥がすことが可能な易剥離性が確保されている。
したがって、プリプレグ複合テープ10は、図1に例示したように巻回状態にしたときに、フィルム12の表面12aに接触するプリプレグテープ11がフィルム12に容易に粘着せず、粘着しても簡単に引き剥がすことができる。
In the prepreg composite tape 10, the film 12 is adhered to the prepreg tape 11 by the adhesive force of the uncured prepreg tape 11.
The surface of the film 12 opposite to the prepreg tape 11 (hereinafter referred to as the surface 12a) is subjected to a silicon treatment. The entire surface 12a of the film 12 is a surface treated with silicone. The film 12 does not easily adhere to the prepreg tape 11 even when the uncured prepreg tape 11 comes into contact with the surface 12a, and is easily peelable even if it adheres. .
Accordingly, when the prepreg composite tape 10 is wound as shown in FIG. 1, the prepreg tape 11 that comes into contact with the surface 12a of the film 12 does not easily adhere to the film 12 and can be easily adhered. Can be peeled off.
一方、フィルム12の表面12aとは反対の裏面(貼着面12b)には、プリプレグテープ11からの剥離性を確保するための処理(シリコ−ン処理等)は施されていない。フィルム12は、その貼着面12b側のプリプレグテープ11に該プリプレグテープ11の粘着力によって貼着状態が安定に保たれる。
このため、プリプレグ複合テープ10は、該プリプレグ複合テープ10を巻回状態にしたプリプレグテープ巻回体21から引き出す際に、フィルム12がその表面12aに接するプリプレグテープ11の粘着力によって、貼着面12b側のプリプレグテープ11から引き剥がされるといった不都合が生じない。プリプレグ複合テープ10は、そのプリプレグテープ巻回体21から引き出す作業を、フィルム12がその貼着面12b側のプリプレグテープ11と一体の状態を保ったまま楽に行うことができる。
On the other hand, the back surface (sticking surface 12b) opposite to the front surface 12a of the film 12 is not subjected to a treatment (silicone treatment or the like) for ensuring peelability from the prepreg tape 11. The adhesive state of the film 12 is stably maintained by the adhesive force of the prepreg tape 11 on the prepreg tape 11 on the adhesive surface 12b side.
For this reason, when the prepreg composite tape 10 is pulled out from the prepreg tape wound body 21 in which the prepreg composite tape 10 is wound, the adhesive surface of the prepreg tape 11 in contact with the surface 12a of the film 12 is attached. There is no inconvenience of being peeled off from the prepreg tape 11 on the 12b side. The prepreg composite tape 10 can be easily pulled out from the prepreg tape winding body 21 while the film 12 is kept integrated with the prepreg tape 11 on the sticking surface 12b side.
図1に示すプリプレグテープ巻回体21(以下、単に巻回体とも言う)は、プリプレグ複合テープ10を巻回状態にしたものである。
図1に例示した巻回体21は、プリプレグ複合テープ10を、そのフィルム12がプリプレグテープ11の湾曲の外周側に位置する向きで巻き上げて巻回状態にしたものである。プリプレグ複合テープ10は、例えば巻芯に巻いて巻回体にすることができる。
この巻回体21は、その外周全周にわたってフィルム12が露出した状態になっており、プリプレグテープ11の露出部分が、プリプレグ複合テープ10の巻回軸線方向両側の端面と、巻回体21外周に位置する巻回終端の端面とに限定されている。このため、この巻回体21は、プリプレグテープ11のフィルム12とは反対側の面(プリプレグテープ11の表面11a)への埃等の付着を防止できるといった利点がある。
A prepreg tape winding body 21 (hereinafter also simply referred to as a winding body) shown in FIG. 1 is obtained by winding a prepreg composite tape 10.
The wound body 21 illustrated in FIG. 1 is obtained by winding the prepreg composite tape 10 in a direction in which the film 12 is wound in the direction in which the film 12 is positioned on the outer peripheral side of the curve of the prepreg tape 11. For example, the prepreg composite tape 10 can be wound around a core to form a wound body.
The wound body 21 is in a state in which the film 12 is exposed over the entire outer periphery of the wound body 21, and the exposed portion of the prepreg tape 11 includes end faces on both sides in the winding axis direction of the prepreg composite tape 10 and the outer periphery of the wound body 21. It is limited to the end surface of the winding end located in the area. For this reason, the wound body 21 has an advantage that dust and the like can be prevented from adhering to the surface of the prepreg tape 11 opposite to the film 12 (surface 11a of the prepreg tape 11).
なお、プリプレグ複合テープ10を巻回状態とした巻回体としては、図5に示すように、プリプレグ複合テープ10を、そのフィルム12がプリプレグテープ11の湾曲の内周側に位置する向きで巻き上げて巻回状態にしたもの(巻回体22)としても良い。
但し、巻回体の取り扱い性の確保の点では、図1に例示した巻回体21の方が、巻回体22に比べてプリプレグテープ11の露出部分が少ない分、有利である。
As a wound body in which the prepreg composite tape 10 is wound, the prepreg composite tape 10 is wound up in such a direction that the film 12 is positioned on the inner peripheral side of the prepreg tape 11 as shown in FIG. It is good also as what was made into the winding state (winding body 22).
However, in terms of ensuring the handleability of the wound body, the wound body 21 illustrated in FIG. 1 is more advantageous because the exposed portion of the prepreg tape 11 is smaller than the wound body 22.
図2、図3、図4は、プリプレグ複合テープ10のプリプレグテープ11を被着物30に接着固定(固定施工)する作業の一例を説明する図である。
図中、被着物30は、コンクリート構造物を例示しているが、被着物30としてはコンクリート構造物に限定されず、例えば金属板、ガラス板等、適宜選択可能である。
2, 3, and 4 are diagrams illustrating an example of an operation for bonding and fixing (fixing) the prepreg tape 11 of the prepreg composite tape 10 to the adherend 30.
In the figure, the adherend 30 illustrates a concrete structure, but the adherend 30 is not limited to a concrete structure, and may be appropriately selected from, for example, a metal plate and a glass plate.
ここで説明するプリプレグ複合テープ10のプリプレグテープ11の被着物30への接着固定作業は、まず、図2、図3に示すように、プリプレグ複合テープ10のプリプレグテープ11のフィルム12とは反対側の表面11aを被着物30表面に密着させ、この状態を維持したまま光照射によってプリプレグテープ11の光硬化性樹脂組成物を硬化させる。 The operation of bonding and fixing the prepreg composite tape 10 to the adherend 30 of the prepreg tape 11 described here is first performed on the side opposite to the film 12 of the prepreg tape 11 of the prepreg composite tape 10 as shown in FIGS. The surface 11a is closely adhered to the surface of the adherend 30, and the photocurable resin composition of the prepreg tape 11 is cured by light irradiation while maintaining this state.
フィルム12は、光透過性のプラスチック製フィルム、より詳しくは、既述の通り、光硬化性樹脂組成物に含まれる光重合開始剤の感光波長域の光に対して実質的に透明のプラスチック製フィルムである。このため、プリプレグ複合テープ10は、被着物30にプリプレグテープ11を密着させた状態で、該プリプレグ複合テープ10のフィルム12側から、光重合開始剤の感光波長域を含む光Hを照射すれば、前記光Hをフィルム12を介して(透過させて)プリプレグテープ11に照射することができ、プリプレグテープ11の光硬化性樹脂組成物を硬化させることができる。 The film 12 is a light-transmitting plastic film, more specifically, as described above, made of a plastic that is substantially transparent to light in the photosensitive wavelength region of the photopolymerization initiator contained in the photocurable resin composition. It is a film. For this reason, if the prepreg composite tape 10 is irradiated with the light H including the photosensitive wavelength region of the photopolymerization initiator from the film 12 side of the prepreg composite tape 10 in a state where the prepreg tape 11 is in close contact with the adherend 30. The light H can be irradiated (transmitted) through the film 12 to the prepreg tape 11, and the photocurable resin composition of the prepreg tape 11 can be cured.
図1に示すように、プリプレグ複合テープ10のその巻回体(巻回体21又は巻回体22)から引き出した部分は、プリプレグテープ11の片面のみにフィルム12が貼着された構成であり、プリプレグテープ11のフィルム12とは反対側の表面11aを覆うものは存在せず、プリプレグテープ11の表面11aが露出した状態となっている。
したがって、プリプレグ複合テープ10は、その巻回体から引き出して、プリプレグテープ11の被着物30への接着固定作業に用いる場合に、図6に例示した従来構成の複合テープ130のようにプリプレグテープの両面のフィルムの片方をプリプレグテープから引き剥がしてプリプレグテープを露出させる作業を行う必要がない。巻回体から引き出したプリプレグ複合テープ10は、従来構成の複合テープのようにフィルムを引き剥がす作業を行うことなく、プリプレグテープ11の表面11aを被着物30に密着させる作業を開始できるから、従来構成の複合テープに比べて、プリプレグテープ11の被着物30への接着固定作業の工程を削減でき、作業時間を短縮できる。
As shown in FIG. 1, the portion of the prepreg composite tape 10 drawn from the wound body (the wound body 21 or the wound body 22) has a configuration in which the film 12 is attached to only one surface of the prepreg tape 11. There is nothing that covers the surface 11a of the prepreg tape 11 opposite to the film 12, and the surface 11a of the prepreg tape 11 is exposed.
Accordingly, when the prepreg composite tape 10 is pulled out from the wound body and used for bonding and fixing the prepreg tape 11 to the adherend 30, the prepreg tape 10 can be made of a prepreg tape like the conventional composite tape 130 illustrated in FIG. 6. There is no need to peel off one of the double-sided films from the prepreg tape to expose the prepreg tape. Since the prepreg composite tape 10 pulled out from the wound body can start the work of bringing the surface 11a of the prepreg tape 11 into close contact with the adherend 30 without performing the work of peeling off the film as in the case of a composite tape having a conventional configuration, Compared to the composite tape having the configuration, the process of bonding and fixing the prepreg tape 11 to the adherend 30 can be reduced, and the working time can be shortened.
光照射Hによるプリプレグテープ11の光硬化性樹脂組成物の硬化が完了したら、次いで、フィルム12をプリプレグテープ11から引き剥がす。これにより、プリプレグテープ11の被着物30への接着固定が完了する。
フィルム12は、プリプレグテープ11が光照射によって硬化して粘着力を喪失することで、プリプレグテープ11からの引き剥がしを弱い力で楽に行える。
When the curing of the photocurable resin composition of the prepreg tape 11 by light irradiation H is completed, the film 12 is then peeled off from the prepreg tape 11. Thereby, the adhesive fixing of the prepreg tape 11 to the adherend 30 is completed.
The film 12 can be easily peeled off from the prepreg tape 11 with a weak force when the prepreg tape 11 is cured by light irradiation and loses adhesive force.
従来構成の複合テープ130は、プリプレグテープの両面から引き剥がしたフィルムの現場からの撤去、廃棄が必要であるが、プリプレグ複合テープ10はプリプレグテープ11の片面のみにフィルム12が貼着されている構成であるため、従来構成の複合テープ130に比べて、プリプレグテープから引き剥がしたフィルムの量を半減させることができる。このため、プリプレグ複合テープ10は、プリプレグテープ11の被着物30への接着固定作業に伴う廃棄物の発生量の削減にも有効に寄与する。 The composite tape 130 of the conventional configuration requires removal and disposal of the film peeled off from both sides of the prepreg tape, and the prepreg composite tape 10 has the film 12 attached to only one side of the prepreg tape 11. Since it is a structure, compared with the composite tape 130 of the conventional structure, the amount of the film peeled off from the prepreg tape can be halved. For this reason, the prepreg composite tape 10 also contributes effectively to a reduction in the amount of waste generated due to the work of fixing the prepreg tape 11 to the adherend 30.
プリプレグ複合テープ10は、プリプレグテープ11の片面のみにフィルム12が貼着されている構成であるため、プリプレグテープの厚みに対するフィルムを含む全体(プリプレグ複合テープ全体)の厚みを、図6に例示した従来構成の複合テープ130に比べて小さくできる。このため、プリプレグ複合テープ10は、図6に例示した従来構成の複合テープ130に比べて、巻回体にしたときの内周側と外周側との周長差の縮小を容易に実現でき、巻回体にしたときの巻き皺の発生防止を容易に実現できる。
また、プリプレグ複合テープ10は、プリプレグテープの両面にフィルムが貼着されている従来構成の複合テープ130に比べてフィルムを節約できる分、低コスト化を容易に実現できる。
Since the prepreg composite tape 10 has a configuration in which the film 12 is adhered to only one surface of the prepreg tape 11, the thickness of the entire film including the film relative to the thickness of the prepreg tape (the entire prepreg composite tape) is illustrated in FIG. It can be made smaller than the composite tape 130 of the conventional configuration. For this reason, the prepreg composite tape 10 can easily realize a reduction in the circumferential length difference between the inner peripheral side and the outer peripheral side when the wound body is made, compared to the composite tape 130 having the conventional configuration illustrated in FIG. It is possible to easily prevent the occurrence of curl when used as a wound body.
Further, the prepreg composite tape 10 can easily realize cost reduction because the film can be saved as compared with the composite tape 130 having a conventional configuration in which films are attached to both surfaces of the prepreg tape.
また、プリプレグ複合テープ10は、従来構成の複合テープ130に比べて、巻回体にしたときのプリプレグテープの長さに対する巻き径の縮小を容易に実現できる。
プリプレグ複合テープ10を巻回体にしたときのプリプレグテープの長さに対する巻き径の縮小は、プリプレグテープの厚みに対するフィルムを含む全体(プリプレグ複合テープ全体)の厚みを抑えることが可能であることが有効に寄与する。
また、プリプレグ複合テープ10は、従来構成の複合テープ130に比べて、プリプレグテープの厚みに対する巻回体の内径の縮小、巻回体の作製に使用する巻芯の外径縮小に有利であり、巻回体の内径縮小によって、プリプレグテープの長さに対する巻き径の縮小を実現することも可能である。プリプレグ複合テープ10は、プリプレグテープの厚みに対する巻回体の内径の、巻き皺の発生を防止可能な限界値を従来構成の複合テープ130に比べて小さくすることができる。プリプレグ複合テープ10を用いて作製する巻回体は、巻き皺の発生を防止可能な範囲でその内径を小さくすることで、巻き皺の発生防止と、プリプレグテープの長さに対する巻き径の縮小とを実現できる。
In addition, the prepreg composite tape 10 can easily reduce the winding diameter with respect to the length of the prepreg tape when the prepreg composite tape 10 is a wound body, as compared with the composite tape 130 having the conventional configuration.
The reduction of the winding diameter with respect to the length of the prepreg tape when the prepreg composite tape 10 is wound may be able to suppress the thickness of the entire film including the film with respect to the thickness of the prepreg tape (the entire prepreg composite tape). Contributes effectively.
Further, the prepreg composite tape 10 is advantageous in reducing the inner diameter of the wound body relative to the thickness of the prepreg tape, and reducing the outer diameter of the core used for producing the wound body, as compared with the composite tape 130 of the conventional configuration. By reducing the inner diameter of the wound body, it is possible to reduce the winding diameter with respect to the length of the prepreg tape. The prepreg composite tape 10 can reduce the limit value of the inner diameter of the wound body relative to the thickness of the prepreg tape, which can prevent the occurrence of curling, as compared with the composite tape 130 of the conventional configuration. The wound body produced using the prepreg composite tape 10 has a reduced inner diameter within a range that can prevent the occurrence of curling, thereby preventing the occurrence of curling and reducing the winding diameter with respect to the length of the prepreg tape. Can be realized.
10…プリプレグ複合テープ、11…光硬化性プリプレグテープ、11a…(光硬化性プリプレグテープの)表面、12…フィルム、12a…(フィルムの)表面、12b…(フィルムの)貼着面、21、22…プリプレグテープ巻回体、30…被着物(コンクリート構造物)。 DESCRIPTION OF SYMBOLS 10 ... Prepreg composite tape, 11 ... Photocurable prepreg tape, 11a ... (Photocurable prepreg tape) surface, 12 ... Film, 12a ... (Film) surface, 12b ... (Film) sticking surface, 21, 22 ... prepreg tape wound body, 30 ... adherend (concrete structure).
Claims (3)
前記プリプレグ複合テープは、光硬化性プリプレグテープの片面のみに、光透過性を有する剥離性のフィルムが貼着され、
前記光硬化性プリプレグテープは、液状の光硬化性樹脂組成物をガラス繊維からなる基材に含浸させて構成され、
前記光硬化性樹脂組成物はエポキシアクリレート樹脂からなり、熱可塑性樹脂粒子をゲル化剤として配合して増粘され、
前記フィルムは、前記光硬化性プリプレグテープに接する貼着面とは反対の表面側にのみシリコーン処理が施されていることを特徴とするプリプレグテープ巻回体。 A prepreg tape wound body obtained by winding a prepreg composite tape,
The prepreg composite tape has a light-peelable peelable film attached to only one side of the photocurable prepreg tape,
The photocurable prepreg tape is constituted by impregnating a substrate made of glass fiber with a liquid photocurable resin composition,
The photocurable resin composition is composed of an epoxy acrylate resin, and is thickened by blending thermoplastic resin particles as a gelling agent.
The prepreg tape wound body , wherein the film is subjected to silicone treatment only on the surface side opposite to the sticking surface in contact with the photocurable prepreg tape.
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