JPH07114832A - Self-bonding UV-curable enameled wire - Google Patents
Self-bonding UV-curable enameled wireInfo
- Publication number
- JPH07114832A JPH07114832A JP26250593A JP26250593A JPH07114832A JP H07114832 A JPH07114832 A JP H07114832A JP 26250593 A JP26250593 A JP 26250593A JP 26250593 A JP26250593 A JP 26250593A JP H07114832 A JPH07114832 A JP H07114832A
- Authority
- JP
- Japan
- Prior art keywords
- curable
- weight
- resin composition
- self
- enameled wire
- 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
- 239000011342 resin composition Substances 0.000 claims abstract description 24
- 239000004020 conductor Substances 0.000 claims abstract description 16
- 210000003298 dental enamel Anatomy 0.000 claims abstract description 13
- 239000012948 isocyanate Substances 0.000 claims abstract description 12
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 12
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 238000004132 cross linking Methods 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 230000001771 impaired effect Effects 0.000 abstract description 2
- 238000003466 welding Methods 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 14
- 229920001187 thermosetting polymer Polymers 0.000 description 9
- 239000003999 initiator Substances 0.000 description 8
- 239000002966 varnish Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 4
- CEXQWAAGPPNOQF-UHFFFAOYSA-N 2-phenoxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOC1=CC=CC=C1 CEXQWAAGPPNOQF-UHFFFAOYSA-N 0.000 description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 3
- 239000012965 benzophenone Substances 0.000 description 3
- 229940119545 isobornyl methacrylate Drugs 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- -1 benzoyl methyl Chemical group 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 1
- AZYRZNIYJDKRHO-UHFFFAOYSA-N 1,3-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC(C(C)(C)N=C=O)=C1 AZYRZNIYJDKRHO-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 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
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 229910000952 Be alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N Methyl benzoate Natural products COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 229960002130 benzoin Drugs 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
- 239000002981 blocking agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000003933 environmental pollution control Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 239000012793 heat-sealing layer Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920003055 poly(ester-imide) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Organic Insulating Materials (AREA)
- Insulated Conductors (AREA)
Abstract
(57)【要約】
【目的】 自己融着可能な紫外線硬化エナメル線を提供
する。
【構成】 導体1にウレタンアクリレート系紫外線硬化
樹脂組成物2を被覆してなる紫外線硬化エナメル線にお
いて、樹脂組成物2中に少なくとも0.5重量%以上の
イソシアネートが含有されていることを特徴とする。樹
脂組成物2中のイソシアネート含有量を0.5重量%以
上とすることで、加熱処理によるアロハネート結合を利
用したエナメル線同士の接着が実現される。また、樹脂
組成物2中のイソシアネート含有量が10重量%以下で
あれば、紫外線架橋樹脂組成物本来の特性を損なわな
い。
(57) [Summary] [Purpose] To provide a self-welding UV-curable enameled wire. A UV curable enamel wire comprising a conductor 1 coated with a urethane acrylate UV curable resin composition 2, wherein the resin composition 2 contains at least 0.5% by weight of isocyanate. To do. By setting the isocyanate content in the resin composition 2 to 0.5% by weight or more, the adhesion of the enameled wires utilizing the alohanate bond by the heat treatment is realized. Further, when the isocyanate content in the resin composition 2 is 10% by weight or less, the original characteristics of the ultraviolet-crosslinking resin composition are not impaired.
Description
【0001】[0001]
【産業上の技術分野】本発明は自己融着紫外線硬化エナ
メル線に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a self-bonding UV-curable enameled wire.
【0002】[0002]
【従来の技術】エナメル線の一つに自己融着エナメル線
がある。自己融着エナメル線は、処理ワニスを使用する
ことなく熱、溶剤によりエナメル線同志を固着できる特
徴をもっており、電気機器、通信機器のコイル形成工程
の省力化、簡略化あるいは機器類のワニス含浸処理工程
の安全性および環境汚染対策の見地から使用されてい
る。この自己融着エナメル線の熱融着層には、主として
ポリビニルブチラール樹脂、ポリビニルホルマール樹
脂、共重合ナイロン及びフェノキシ樹脂等が用いられて
いる。特に共重合ナイロンが広く使用され、6−66,
6−12ナイロン重合体及びナイロン12を組み合わせ
ることにより得られる熱変形の少ないエナメル線が用い
られている。またフェノール樹脂等により変性すること
により低温で融着可能なエナメル線も用いられている。2. Description of the Related Art One of the enameled wires is a self-bonding enameled wire. The self-fusing enameled wire has the characteristic that both enameled wires can be fixed together by heat and solvent without using a treated varnish, which reduces the labor and simplification of the coil forming process of electrical equipment and communication equipment, or impregnates the equipment with varnish. It is used from the standpoint of process safety and environmental pollution control. Polyvinyl butyral resin, polyvinyl formal resin, copolymerized nylon, phenoxy resin and the like are mainly used for the heat-sealing layer of the self-bonding enameled wire. Especially, copolymerized nylon is widely used.
An enameled wire having a small thermal deformation obtained by combining a 6-12 nylon polymer and nylon 12 is used. Further, an enameled wire that can be fused at a low temperature by being modified with a phenol resin or the like is also used.
【0003】しかしながら、自己融着エナメルは絶縁層
としてあまり寄与しないため、一般に従来のエナメル線
上に塗布して用いられている。However, since the self-fusing enamel does not contribute much as an insulating layer, it is generally used by coating it on a conventional enamel wire.
【0004】従来のエナメル線の多くは熱硬化型の材料
(熱硬化型ワニス)が使用されている。熱硬化型ワニス
には、エポキシ系、シリコーン系、ポリウレタン系、ポ
リエステル系、ポリアミドイミド系、ポリイミド系、ポ
リエステルイミド系、ホルマール系などがある。これら
はほとんど溶剤を用いた塗料で、多くのものが50%以
上有機溶剤が占める材料のため、通常塗布焼き付け工程
を5回以上繰り返し行う必要があり、また溶剤を用いて
いるため大掛かりな安全設備(溶剤の回収・焼却等)を
必要とするなど、作業環境上好ましくない。自己融着エ
ナメルについても同様である。Most of the conventional enameled wires use a thermosetting material (thermosetting varnish). The thermosetting varnish includes epoxy type, silicone type, polyurethane type, polyester type, polyamide imide type, polyimide type, polyester imide type, and formal type. Most of these are paints that use a solvent, and since most of them are materials in which 50% or more of the organic solvent is used, it is usually necessary to repeat the coating and baking process five times or more. Also, since a solvent is used, large-scale safety equipment is required. It is not preferable in the work environment because it requires (solvent collection, incineration, etc.). The same applies to the self-bonding enamel.
【0005】こうした溶剤を用いない塗料として注目さ
れているのが無溶剤で液状の紫外線硬化塗料である。紫
外線硬化塗料は無溶剤のため熱硬化型ワニスに比べ安全
性が高く、1回ないし数回の塗布により厚膜を得ること
ができる。また、熱硬化型ワニスに比べ硬化性に優れた
ものが得られやすく生産性に大きな効果をもつほか、無
色透明な塗料とすることで熱硬化型ワニスに比べ着色が
容易である。Attention is paid to a solventless liquid UV curable coating material as a coating material which does not use such a solvent. Since the ultraviolet curable coating is solvent-free, it is more safe than the thermosetting varnish, and a thick film can be obtained by applying the coating once or several times. Further, in comparison with the thermosetting varnish, it is easy to obtain a curable product having a great curability, which has a great effect on productivity, and the colorless and transparent coating material makes it easier to color than the thermosetting varnish.
【0006】[0006]
【発明が解決しようとする課題】しかし、一般に、紫外
線硬化塗料はエナメル線の熱硬化型ワニスと同様に、硬
化時に三次元の架橋体を形成し、硬化後は熱で熔融しな
いため、紫外線硬化塗料を被覆したエナメル線を熱融着
することができなという問題があった。However, in general, an ultraviolet curable coating material forms a three-dimensional crosslinked body at the time of curing as in the case of a thermosetting varnish for an enameled wire, and does not melt by heat after curing, so that it is ultraviolet cured. There was a problem that the enamel wire coated with the paint could not be heat-sealed.
【0007】本発明の目的は、前記した従来技術の問題
点を解消し、自己融着可能な紫外線硬化エナメル線を提
供することにある。An object of the present invention is to solve the above-mentioned problems of the prior art and to provide an ultraviolet curable enameled wire capable of self-bonding.
【0008】[0008]
【課題を解決するための手段】上記のような課題を解決
すべく紫外線硬化塗料について種々の検討を行った結
果、ウレタンアクリレート系紫外線硬化樹脂組成物中に
0.5重量%以上のイソシアネートを添加しておくこと
により自己融着性を付与できることを見いだし、本発明
を完成するに至った。[Means for Solving the Problems] As a result of various studies on an ultraviolet curable coating material to solve the above problems, 0.5% by weight or more of isocyanate was added to a urethane acrylate type ultraviolet curable resin composition. It was found that the self-fusing property can be imparted by preliminarily setting it, and the present invention has been completed.
【0009】すなわち本発明の自己融着紫外線硬化エナ
メル線は、導体にウレタンアクリレート系紫外線硬化樹
脂組成物を被覆してなる紫外線硬化エナメル線を前提と
し、上記樹脂組成物中に少なくとも0.5重量%以上の
イソシアネートが含有されていることを特徴とするもの
である。That is, the self-fusing UV-curable enameled wire of the present invention is based on the UV-curable enameled wire obtained by coating a conductor with a urethane acrylate UV-curable resin composition. % Or more of isocyanate is contained.
【0010】[0010]
【作用】上記ウレタンアクリレート系紫外線架橋樹脂組
成物は、ウレタン(メタ)アクリレートオリゴマを主成
分とし、その他、光重合性モノマや、光重合開始剤等か
らなる樹脂組成物であって、ウレタン(メタ)アクリレ
ートオリゴマがジイソシアネートとポリオールとヒドロ
キシアルキル(メタ)アクリレートから製造されるもの
であればよく、特に限定されるものではない。The above urethane acrylate-based UV-crosslinking resin composition is a resin composition containing a urethane (meth) acrylate oligomer as a main component and other components such as a photopolymerizable monomer and a photopolymerization initiator. ) The acrylate oligomer is not particularly limited as long as it is produced from diisocyanate, polyol and hydroxyalkyl (meth) acrylate.
【0011】光重合モノマとしては、アクリロイル基、
メタクロイル基、アリル基、ビニル基等の不飽和二重結
合を有する官能基をもつ公知の反応性希釈剤等を用いる
ことができる。望ましくは官能基がメタクロイル基の単
官能モノマを用いることが低温半田付性に有効である。The photopolymerizable monomer includes an acryloyl group,
A known reactive diluent having a functional group having an unsaturated double bond such as a methacroyl group, an allyl group and a vinyl group can be used. Desirably, it is effective for low temperature solderability to use a monofunctional monomer whose functional group is a metacroyl group.
【0012】光重合開始剤は特に限定されるものではな
く公知の光重合開始剤を用いればよい。例えばアセトフ
ェノン系、ベンゾイン系、ベンゾフェノン系、チオキサ
ンソン系等がある。アセトフェノン系としては2−ヒド
ロキシ−2−メチル−1−フェニルプロパン−1−オ
ン,1−ヒドロキシシクロヘキシルフェニルケトン、2
−メチル−1−[4−(メチルチオ)フェニル]−2−
モルホリノプロパン−1などがあり、ベンゾフェノン系
としてはベンゾフェノン、ベンゾイル安息香酸メチル、
3.3´−ジメチル−4−メトキシベンゾフェノンなど
があり、チオキサンソン系としては2.4−ジエチルチ
オキサンソン、2.4−ジクロロチオキサンソンなどが
あげられる。The photopolymerization initiator is not particularly limited, and a known photopolymerization initiator may be used. Examples include acetophenone-based, benzoin-based, benzophenone-based, thioxanthone-based and the like. As the acetophenone type, 2-hydroxy-2-methyl-1-phenylpropan-1-one, 1-hydroxycyclohexylphenyl ketone, 2
-Methyl-1- [4- (methylthio) phenyl] -2-
Morpholinopropane-1 and the like, benzophenone-based benzophenone, benzoyl methyl benzoate,
There are 3.3'-dimethyl-4-methoxybenzophenone and the like, and examples of the thioxanthone type include 2.4-diethylthioxanthone and 2.4-dichlorothioxanthone.
【0013】イソシアネートは特に限定されるものでは
ないが、イソシアネート基を少なくとも2個以上有する
ものであればよい。たとえばヘキサメレンジイソシアネ
ート,イソホロンジイソシアネート,m−テトラメチル
キシレンジイソシアネート,p−テトラメチルキシレン
ジイソシアネート,p−フェニレンジイソシアネート,
2.4−トルエンジイソシアネート,ナフタレンジイソ
シアネート,4.4−ジフェニルメタンジイソシアネー
ト,キシレンジイソシアネート,メチレンビス(4−シ
クロヘキシルイソシアネート),トリメチルヘキサメチ
レンジイソシアネート,4.4´−ジフェニルメタント
リイソシアネートなどがあげられる。The isocyanate is not particularly limited as long as it has at least two isocyanate groups. For example, hexamerene diisocyanate, isophorone diisocyanate, m-tetramethyl xylene diisocyanate, p-tetramethyl xylene diisocyanate, p-phenylene diisocyanate,
Examples include 2.4-toluene diisocyanate, naphthalene diisocyanate, 4.4-diphenylmethane diisocyanate, xylene diisocyanate, methylenebis (4-cyclohexyl isocyanate), trimethylhexamethylene diisocyanate, 4.4'-diphenylmethane triisocyanate.
【0014】イソシアネートの添加量を少なくとも0.
5重量%以上としたのはそれより少ないと加熱処理によ
るアロハネート結合を利用したエナメル線同士の接着が
実現されにくいためである。望ましくは1重量%以上1
0重量%以下がよい。10重量%以上では添加量に対す
る効果が小さいことや紫外線架橋樹脂組成物本来の特性
を損なうためである。The amount of isocyanate added is at least 0.
The amount of 5% by weight or more is because if it is less than that, it is difficult to realize the adhesion between the enameled wires utilizing the alohanate bond by the heat treatment. Desirably 1% by weight or more 1
It is preferably 0% by weight or less. This is because if it is 10% by weight or more, the effect on the added amount is small and the original properties of the ultraviolet-crosslinking resin composition are impaired.
【0015】導体を構成する金属は、銅,アルミニウ
ム,鉄,銀,白金等のいずれでもよく、それらの合金、
それらに錫、亜鉛等との合金でもよい。また、それらに
錫、銀、ニッケル等でメッキされたものでもよい。金属
導体は単線であってもよく、撚線や撚線をさらにメッキ
したものでもよい。また平角状の金属導体でもよい。The metal constituting the conductor may be any of copper, aluminum, iron, silver, platinum, etc., and alloys thereof.
They may be alloys with tin, zinc or the like. Further, those plated with tin, silver, nickel or the like may be used. The metal conductor may be a single wire, or a stranded wire or a stranded wire further plated. Alternatively, a rectangular metal conductor may be used.
【0016】このほか必要に応じて光重合開始助剤、接
着防止剤、チクソ付与剤、充填剤、可塑剤、非反応性ポ
リマー、着色剤、難燃剤、難燃助剤、軟化防止剤、離型
剤、乾燥剤、分散剤、湿潤剤、沈澱防止剤、増粘剤、帯
電防止剤、静電防止剤、防かび剤、防鼠剤、防蟻剤、艶
消し剤、ブロッキング防止剤、皮張り防止剤等、その他
諸々の無機化合物、有機化合物を組み合わせて用いるこ
とができる。In addition, if necessary, a photopolymerization initiation auxiliary agent, an adhesion preventive agent, a thixotropic agent, a filler, a plasticizer, a non-reactive polymer, a colorant, a flame retardant, a flame retardant auxiliary agent, an anti-softening agent, a release agent. Molding agent, drying agent, dispersant, wetting agent, anti-settling agent, thickening agent, antistatic agent, antistatic agent, antifungal agent, anti-mouse agent, anti-termite agent, matting agent, anti-blocking agent, skin It is possible to use a combination of various inorganic compounds and organic compounds such as anti-tension agents.
【0017】[0017]
【実施例】次に、本発明の自己融着紫外線硬化エナメル
線の実施例について説明する。EXAMPLES Next, examples of the self-fusing UV-curable enameled wire of the present invention will be described.
【0018】[実施例1]ウレタンアクリレートオリゴ
マーM−1100(東亜合成化学工業(株)製)を10
0重量部、フェノキシエチルメタクリレート50重量
部、イソボルニルメタクリレート30重量部、及び光重
合開始剤の2、2−ジメトキシ−2−フェニルアセトフ
ェノン5重量部及びトルエンジイソシアネート5重量部
からなる紫外線硬化樹脂組成物を裸軟銅線導体0.13
(1/0.13)上に被覆した後、紫外線照射炉を通し
て硬化させ絶縁厚15μmの紫外線硬化エナメル線を得
た。[Example 1] A urethane acrylate oligomer M-1100 (manufactured by Toagosei Kagaku Kogyo Co., Ltd.) was used.
UV curable resin composition consisting of 0 parts by weight, phenoxyethyl methacrylate 50 parts by weight, isobornyl methacrylate 30 parts by weight, and photopolymerization initiator 2,2-dimethoxy-2-phenylacetophenone 5 parts by weight and toluene diisocyanate 5 parts by weight. Bare annealed copper wire conductor 0.13
After coating on (1 / 0.13), it was cured by passing through an ultraviolet irradiation furnace to obtain an ultraviolet curable enamel wire having an insulation thickness of 15 μm.
【0019】[実施例2]ウレタンアクリレートオリゴ
マーM−1100を100重量部、イソボルニルメタク
リレート50重量部、光重合開始剤の2、2−ジメトキ
シー2−フェニルアセトフェノン5重量部及びヘキサメ
チレンジイソシアネート5重量部からなる紫外線硬化樹
脂組成物を裸軟銅線導体0.13(1/0.13)上に
被覆した後、紫外線照射炉を通して硬化させ絶縁厚16
μmの紫外線硬化エナメル線を得た。Example 2 100 parts by weight of urethane acrylate oligomer M-1100, 50 parts by weight of isobornyl methacrylate, 5 parts by weight of photopolymerization initiator 2,2-dimethoxy-2-phenylacetophenone and 5 parts by weight of hexamethylene diisocyanate. After coating the bare annealed copper wire conductor 0.13 (1 / 0.13) with a UV curable resin composition consisting of 10 parts, it is cured through an UV irradiation furnace to obtain an insulation thickness of 16
A UV curable enameled wire of μm was obtained.
【0020】[実施例3]ウレタンアクリレートオリゴ
マーU−122M(新中村化学(株)製)を100重量
部、フェノキシエチルメタクリレート50重量部、イソ
ボルニルメタクリレート50重量部、光重合開始剤の
2、2−ジメトキシ−2−フェニルアセトフェノン5重
量部及びトルエンジイソシアネート10重量部からなる
紫外線硬化樹脂組成物を裸軟銅線導体0.13(1/
0.13)上に被覆した後、紫外線照射炉を通して硬化
させ絶縁厚15μmの紫外線硬化エナメル線を得た。[Example 3] 100 parts by weight of urethane acrylate oligomer U-122M (manufactured by Shin-Nakamura Chemical Co., Ltd.), 50 parts by weight of phenoxyethyl methacrylate, 50 parts by weight of isobornyl methacrylate, 2, a photopolymerization initiator, A UV-curable resin composition comprising 5 parts by weight of 2-dimethoxy-2-phenylacetophenone and 10 parts by weight of toluene diisocyanate was used as a bare annealed copper wire conductor 0.13 (1 /
0.13) and then cured through a UV irradiation furnace to obtain a UV cured enamel wire having an insulation thickness of 15 μm.
【0021】[比較例1]ウレタンアクリレートオリゴ
マーM−1100を100重量部、フェノキシエチルメ
タクリレート50重量部及び光重合開始剤の2、2−ジ
メトキシ−2−フェニルアセトフェノン5重量部からな
る紫外線硬化樹脂組成物を裸軟銅線導体0.13(1/
0.13)上に被覆した後、紫外線照射炉を通して硬化
させ絶縁厚16μmの紫外線硬化エナメル線を得た。Comparative Example 1 An ultraviolet-curable resin composition comprising 100 parts by weight of urethane acrylate oligomer M-1100, 50 parts by weight of phenoxyethyl methacrylate and 5 parts by weight of 2,2-dimethoxy-2-phenylacetophenone as a photopolymerization initiator. Bare annealed copper wire conductor 0.13 (1 /
0.13) and then cured through an ultraviolet irradiation furnace to obtain an ultraviolet curable enamel wire having an insulation thickness of 16 μm.
【0022】[比較例2]ウレタンアクリレートオリゴ
マーM−1100を100重量部、フェノキシエチルメ
タクリレート60重量部、光重合開始剤の2、2−ジメ
トキシ−2−フェニルアセトフェノン5重量部及びトル
エンジイソシアネート5重量部からなる紫外線架橋樹脂
組成物を裸軟銅線導体0.13(1/0.13)上に被
覆した後、紫外線照射炉を通して硬化させ、絶縁厚15
μmの紫外線硬化エナメル線を得た。 以上の実施例1
〜3の紫外線硬化エナメル線及び比較例1,2の紫外線
硬化エナメル線のそれぞれに対し自己融着性について評
価した結果を表1に示す。Comparative Example 2 100 parts by weight of urethane acrylate oligomer M-1100, 60 parts by weight of phenoxyethyl methacrylate, 5 parts by weight of 2,2-dimethoxy-2-phenylacetophenone as a photopolymerization initiator and 5 parts by weight of toluene diisocyanate. A bare annealed copper wire conductor 0.13 (1 / 0.13) is coated with an ultraviolet-crosslinking resin composition consisting of
A UV curable enameled wire of μm was obtained. Example 1 above
Table 1 shows the results of evaluation of the self-bonding property of each of the ultraviolet-curing enameled wires of Nos. 3 to 3 and the ultraviolet-cured enameled wires of Comparative Examples 1 and 2.
【0023】[0023]
【表1】 [Table 1]
【0024】*自己融着性の評価方法* 作成したエナメル線をツバ径40mm、マンドレル径2
0mm、長さ50mmのアルミ製のボビンに線同志が接
触するように巻き付け、このエナメル線を通電加熱によ
り約150℃で10分処理した後、線同志の接着状態を
観察した。* Evaluation method of self-bonding property * Prepared enamel wire with a brim diameter of 40 mm and a mandrel diameter of 2
The wire was wound around an aluminum bobbin having a length of 0 mm and a length of 50 mm so that the wires contact each other, and this enamel wire was treated by electric heating at about 150 ° C. for 10 minutes, and then the bonding state of the wires was observed.
【0025】また、各紫外線硬化樹脂組成物の200μ
m厚のシ−トを作成し、これを幅20mm,長さ100
mmにしたものを2枚重ねて2枚のアルミ金属板の間に
挟み、荷重500gをのせ、150℃で30分加熱処理
した後、接着力をテンシロンで測定した。In addition, 200 μm of each ultraviolet curable resin composition
Create a m-thick sheet and make it 20 mm wide and 100 mm long.
Two pieces having a thickness of 2 mm were stacked and sandwiched between two aluminum metal plates, a load of 500 g was applied, and heat treatment was performed at 150 ° C. for 30 minutes, and then the adhesive force was measured by Tensilon.
【0026】表1から明らかなように、イソシアネート
0.5重量%以上添加した実施例1〜3の紫外線硬化エ
ナメル線はいずれも自己融着が可能であった。また、シ
−トの貼り合わせでイソシアネートの比率が高い方が高
い接着力が得られることがわかる。As is clear from Table 1, all of the UV-curable enameled wires of Examples 1 to 3 to which 0.5% by weight or more of isocyanate was added were capable of self-bonding. Further, it can be seen that, when the sheets are bonded together, the higher the isocyanate ratio, the higher the adhesive strength.
【0027】一方、比較例1,2の紫外線硬化エナメル
線はいずれも自己融着性はなく、シ−トの貼り付けでも
接着力の無いものであった。On the other hand, none of the UV-curable enameled wires of Comparative Examples 1 and 2 had self-bonding property, and there was no adhesive strength even when the sheets were attached.
【0028】なお、本発明の自己融着紫外線硬化エナメ
ル線は、単心のエナメル線以外に、多心のエナメル線に
も適用することができる。図1は1本の導体1に紫外線
硬化樹脂組成物2を被覆してなる単心のエナメル線、図
2は7本の導体1を1つに撚合わせて紫外線硬化樹脂組
成物2で被覆してなる7心のエナメル線の実施例をそれ
ぞれ示している。また、図3は紫外線硬化樹脂又は熱硬
化樹脂3を被覆した7本の導体1を1つに撚合わせて紫
外線硬化樹脂組成物2で被覆した7心のエナメル線の実
施例である。The self-bonding UV-curable enameled wire of the present invention can be applied to a multi-core enameled wire as well as a single-core enameled wire. FIG. 1 is a single-core enamel wire formed by coating one conductor 1 with an ultraviolet curable resin composition 2. In FIG. 2, seven conductors 1 are twisted into one and coated with an ultraviolet curable resin composition 2. Examples of the seven-core enameled wire are shown. FIG. 3 shows an example of a 7-core enameled wire in which seven conductors 1 coated with an ultraviolet curable resin or a thermosetting resin 3 are twisted into one and coated with an ultraviolet curable resin composition 2.
【0029】[0029]
【発明の効果】以上要するに本発明の自己融着紫外線硬
化エナメル線によれば、導体を被覆するウレタンアクリ
レート系紫外線硬化樹脂組成物中に少なくとも0.5重
量%以上のイソシアネートが含有されているので、加熱
処理することによりアロハネート結合を利用してエナメ
ル線同士を融着させることができる。In summary, according to the self-fusing UV-curable enameled wire of the present invention, the urethane acrylate UV-curable resin composition for coating the conductor contains at least 0.5% by weight of isocyanate. The heat treatment makes it possible to fuse the enamel wires to each other by utilizing the alohanate bond.
【図1】本発明の自己融着紫外線硬化エナメル線の一実
施例を示す横断面図である。FIG. 1 is a cross-sectional view showing an example of a self-bonding UV-curable enameled wire of the present invention.
【図2】本発明の自己融着紫外線硬化エナメル線の他の
実施例を示す横断面図である。FIG. 2 is a cross-sectional view showing another embodiment of the self-bonding UV-curable enameled wire of the present invention.
【図3】本発明の自己融着紫外線硬化エナメル線の他の
実施例を示す横断面図である。FIG. 3 is a cross-sectional view showing another embodiment of the self-bonding UV-curable enameled wire of the present invention.
1 導体 2 紫外線硬化樹脂組成物 3 紫外線硬化樹脂又は熱硬化樹脂 1 conductor 2 UV curable resin composition 3 UV curable resin or thermosetting resin
───────────────────────────────────────────────────── フロントページの続き (72)発明者 高畑 紀雄 茨城県日立市日高町5丁目1番1号 日立 電線株式会社パワーシステム研究所内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Norio Takahata 5-1-1 Hidakacho, Hitachi City, Ibaraki Prefecture Hitachi Cable Ltd. Power Systems Research Center
Claims (2)
化樹脂組成物を被覆してなる紫外線硬化エナメル線にお
いて、上記樹脂組成物中に少なくとも0.5重量%以上
のイソシアネートが含有されていることを特徴とする自
己融着紫外線硬化エナメル線。1. An ultraviolet curable enamel wire comprising a conductor coated with a urethane acrylate ultraviolet curable resin composition, wherein the resin composition contains at least 0.5% by weight of isocyanate. Self-bonding UV-curable enameled wire.
量が1重量%以上10重量%以下である請求項1記載の
自己融着紫外線硬化エナメル線。2. The self-bonding UV-curable enameled wire according to claim 1, wherein the content of isocyanate in the resin composition is 1% by weight or more and 10% by weight or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26250593A JPH07114832A (en) | 1993-10-20 | 1993-10-20 | Self-bonding UV-curable enameled wire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26250593A JPH07114832A (en) | 1993-10-20 | 1993-10-20 | Self-bonding UV-curable enameled wire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07114832A true JPH07114832A (en) | 1995-05-02 |
Family
ID=17376741
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26250593A Pending JPH07114832A (en) | 1993-10-20 | 1993-10-20 | Self-bonding UV-curable enameled wire |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07114832A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008251435A (en) * | 2007-03-30 | 2008-10-16 | Jsr Corp | Radiation curable resin composition for wire coating |
| JP4776048B2 (en) * | 1997-10-24 | 2011-09-21 | 古河電気工業株式会社 | Multilayer insulated wire and transformer using the same |
-
1993
- 1993-10-20 JP JP26250593A patent/JPH07114832A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4776048B2 (en) * | 1997-10-24 | 2011-09-21 | 古河電気工業株式会社 | Multilayer insulated wire and transformer using the same |
| JP2008251435A (en) * | 2007-03-30 | 2008-10-16 | Jsr Corp | Radiation curable resin composition for wire coating |
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