JPS62170920A - Optical fiber covered with ultraviolet cured resin - Google Patents
Optical fiber covered with ultraviolet cured resinInfo
- Publication number
- JPS62170920A JPS62170920A JP61012870A JP1287086A JPS62170920A JP S62170920 A JPS62170920 A JP S62170920A JP 61012870 A JP61012870 A JP 61012870A JP 1287086 A JP1287086 A JP 1287086A JP S62170920 A JPS62170920 A JP S62170920A
- Authority
- JP
- Japan
- Prior art keywords
- optical fiber
- resin
- modulus
- young
- ultraviolet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000013307 optical fiber Substances 0.000 title claims abstract description 50
- 239000011347 resin Substances 0.000 title claims abstract description 49
- 229920005989 resin Polymers 0.000 title claims abstract description 49
- 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 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229920005906 polyester polyol Polymers 0.000 claims abstract description 5
- 150000003077 polyols Chemical group 0.000 claims abstract description 5
- 238000000576 coating method Methods 0.000 claims description 51
- 239000011248 coating agent Substances 0.000 claims description 50
- 239000000463 material Substances 0.000 claims description 10
- 230000005540 biological transmission Effects 0.000 abstract description 18
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 239000000835 fiber Substances 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 12
- 230000003287 optical effect Effects 0.000 description 8
- 239000002966 varnish Substances 0.000 description 8
- 239000010410 layer Substances 0.000 description 6
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical group OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical group CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- HCLJOFJIQIJXHS-UHFFFAOYSA-N 2-[2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOCCOC(=O)C=C HCLJOFJIQIJXHS-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- -1 polytetramethylene Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 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 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 1
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
- FJFVXUURYJTNOJ-UHFFFAOYSA-N 2-(2-hydroxyethoxy)-1-phenylethanol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCCOCC(O)C1=CC=CC=C1 FJFVXUURYJTNOJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- HBUCNDYVFHQFMB-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]-1-phenylethanol;prop-2-enoic acid Chemical compound OC(=O)C=C.OCCOCCOCC(O)C1=CC=CC=C1 HBUCNDYVFHQFMB-UHFFFAOYSA-N 0.000 description 1
- WVRHNZGZWMKMNE-UHFFFAOYSA-N 2-hydroxy-1-[2-(2-methylpropyl)phenyl]-2-phenylethanone Chemical compound CC(C)CC1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 WVRHNZGZWMKMNE-UHFFFAOYSA-N 0.000 description 1
- NACPTFCBIGBTSJ-UHFFFAOYSA-N 2-hydroxy-2-phenyl-1-(2-propan-2-ylphenyl)ethanone Chemical compound CC(C)C1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 NACPTFCBIGBTSJ-UHFFFAOYSA-N 0.000 description 1
- KJCFAQDTHMIAAN-UHFFFAOYSA-N 2-methyl-1-phenylprop-2-en-1-one Chemical compound CC(=C)C(=O)C1=CC=CC=C1 KJCFAQDTHMIAAN-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229920000562 Poly(ethylene adipate) Polymers 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 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
- ZNAAXKXXDQLJIX-UHFFFAOYSA-N bis(2-cyclohexyl-3-hydroxyphenyl)methanone Chemical compound C1CCCCC1C=1C(O)=CC=CC=1C(=O)C1=CC=CC(O)=C1C1CCCCC1 ZNAAXKXXDQLJIX-UHFFFAOYSA-N 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
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- FZWBABZIGXEXES-UHFFFAOYSA-N ethane-1,2-diol;hexanedioic acid Chemical compound OCCO.OC(=O)CCCCC(O)=O FZWBABZIGXEXES-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
Landscapes
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は紫外線硬化樹脂被覆光ファイバーに関する。さ
らに詳しくは、樹脂被覆を有する低温特性にすぐれた石
英ガラス系光ファイバーに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an optical fiber coated with an ultraviolet curing resin. More specifically, the present invention relates to a silica glass optical fiber coated with resin and having excellent low-temperature properties.
[従来の技術]
石英ガラス系光ファイバーには、外部よりのカヤ衝撃か
ら光ファイバーを保護するために多層の樹脂被覆が設け
られている。これらの樹脂被覆は通常、光フアイバー直
上に設けられる1次被覆J3よびその外側に設けられる
2次被覆から構成されており、要するば1次被覆と2次
被覆との間にバッファ層が設【プられていることもある
。[Prior Art] A silica glass optical fiber is provided with a multilayer resin coating to protect the optical fiber from external impact. These resin coatings usually consist of a primary coating J3 provided directly above the optical fiber and a secondary coating provided outside it.In other words, a buffer layer is provided between the primary coating and the secondary coating. Sometimes it's even pulled.
光ファイバーは種々の環境で使用され、それぞれの環境
において要求される特性を有するように改良されている
。たとえば、厳寒地域などのような低2H(−io℃以
下)で使用されるばあい、光伝送損失が大きくなる。こ
の現象は、樹脂被覆の収縮により光ファイバーにマイク
ロベンディングが生ずるからであると考えられており、
1次被覆として常温で1〜100Nf/mのヤング率を
有しかつ低温(約−30℃)でもヤング率がほとんど変
化しないような柔かい樹脂が用いられている。Optical fibers are used in various environments and are improved to have the characteristics required in each environment. For example, when used at low 2H (below -io°C), such as in extremely cold regions, optical transmission loss increases. This phenomenon is thought to be due to microbending occurring in the optical fiber due to shrinkage of the resin coating.
A soft resin having a Young's modulus of 1 to 100 Nf/m at room temperature and whose Young's modulus hardly changes even at low temperatures (about -30° C.) is used as the primary coating.
[発明により解決しようとする問題点コしかしながら、
低温でも小さいヤング率を有するような樹脂を1次被覆
剤として用いても光ファイバーの低温での光伝送損失の
増加は依然として存在している。[The problems that the invention attempts to solve, however,
Even if a resin having a small Young's modulus even at low temperatures is used as the primary coating material, the optical fiber's optical transmission loss at low temperatures still increases.
本発明者らは、低温でヤング率が増大するような樹脂で
あっても特定のヤング率を有するものは、前記のごとき
光伝送損失の大幅な増大を招かないどころかヤング率の
殆んど変化しないものよりも低温での損失増加が少なく
なるというおどろくべき事実を見出し、本発明を完成す
るに至った。The present inventors have found that even if the resin has a specific Young's modulus, even if the Young's modulus increases at low temperatures, it will not cause a significant increase in optical transmission loss as described above, and will hardly change the Young's modulus. We have discovered the surprising fact that the increase in loss at low temperatures is smaller than those without, and have completed the present invention.
[問題点を解決するための手段]
すべりち本発明は、紫外線硬化性樹脂の紫外I!硬化物
で1次被覆および2次被覆が形成されている石英ガラス
系光ファイバーであって、1次被覆の紫外線硬化物が2
5℃および一30℃でそれぞれ10〜100Ny/dお
よび100〜20.000Kg / cdのヤング率を
有し、かつ2次被覆の紫外線硬化物が25℃で1 、0
00〜20.000に9 / dのヤング率を有する紫
外線硬化樹脂被覆光ファイバーに関する。[Means for Solving the Problems] The present invention provides ultraviolet I! of ultraviolet curing resin. A silica glass optical fiber in which the primary coating and the secondary coating are formed of a cured product, and the primary coating is made of an ultraviolet cured product.
It has a Young's modulus of 10 to 100 Ny/d and 100 to 20.000 Kg/cd at 5°C and -30°C, respectively, and the UV-cured product of the secondary coating has a modulus of 1.0 at 25°C.
It relates to an ultraviolet curing resin coated optical fiber having a Young's modulus of 9/d between 00 and 20.000.
〔作用および実施例]
本発明の樹脂被覆光ファイバーの大きな特徴は、従来低
温時の光伝送損失を増大させると考えられていた低温時
にヤング率の増大する樹脂を1次被覆に用いる点にあり
、2次被覆用の樹脂としては1 、000〜20,0O
OKfl/ai程度のヤング率を有する従来から使用さ
れている紫外線硬化樹脂が使用できる。[Operations and Examples] A major feature of the resin-coated optical fiber of the present invention is that a resin whose Young's modulus increases at low temperatures, which was conventionally thought to increase optical transmission loss at low temperatures, is used for the primary coating. The resin for secondary coating is 1,000 to 20,00
A conventionally used ultraviolet curing resin having a Young's modulus of about OKfl/ai can be used.
特定のヤング率の温度依存性を有する紫外線硬化樹脂を
1次被覆として用いると光伝送損失の増大が小さくなる
理由は未だ朗らかではないが、俊述する実施例に示され
ているごとく、すぐれた効果がえられる。The reason why the increase in optical transmission loss is reduced when an ultraviolet curable resin with a specific temperature dependence of Young's modulus is used as the primary coating is not yet clear, but as shown in the examples to be described, excellent You can get the effect.
本発明が対象とする光ファイバーは、石英ガラス系光フ
ァイバーである限り、その構造やモジュールは問わない
。The structure and module of the optical fiber to which the present invention is directed does not matter, as long as it is a silica glass optical fiber.
本発明の重要な特徴である1次被覆の形成に用いる紫外
wATa化性の樹脂は、前記のごとく、その紫外線硬化
物が25℃において10〜100Kg/ ad 、好ま
しくは30〜80Kg/cjA1とくに好ましくは65
〜80に9/ctdのヤング率を有し、かつ−30℃と
いう低温でヤング率が増大して100〜20、 OOO
Ng/ cd 、好ましくは500〜5.000kg/
ci、とくに好ましくは1.000〜3.000Kg
/ cdとなるものである。この範囲のヤング率NU依
存性を有するものは、意外にも低温時の光伝送特性が従
来のものよりも優れている。1次被覆形成用の紫外[[
!化性樹脂としては、たとえばウレタンアクリレート系
、ポリブタジェンアクリレート系、シリコーンアクリレ
ート系、ポリエステルアクリレート系、エポキシアクリ
レート系、ポリエーテルアクリレート系などの紫外線硬
化性樹脂があげられる。それらのうちウレタンアクリレ
ート系樹脂が好ましく、とくにポリエステルポリオール
単位を少なくとも1個含むウレタンアクリレートオリゴ
マーを含有しているものが好ましい。たとえば、ポリオ
ール成分がポリテトラメチレングリコール(PTMG)
およびアジピン酸と1.6−ヘキサンジオールのポリエ
ステルポリオールからなり、イソシアネート成分がイソ
ホロンジイソシアネート(IPDI) 、アクリレート
成分が2−ヒドロキシエチルアクリレート(HEA)で
あるものが好ましい。As mentioned above, the UV-curable resin used for forming the primary coating, which is an important feature of the present invention, has an ultraviolet cured product of 10 to 100 Kg/ad, preferably 30 to 80 Kg/cjA1, at 25°C. is 65
It has a Young's modulus of ~80 to 9/ctd, and the Young's modulus increases at a low temperature of -30°C to 100 to 20, OOO
Ng/cd, preferably 500-5.000kg/
ci, particularly preferably 1.000 to 3.000Kg
/ CD. Those having a Young's modulus NU dependence in this range surprisingly have better optical transmission characteristics at low temperatures than conventional ones. Ultraviolet light for primary coating formation [[
! Examples of the curing resin include UV curable resins such as urethane acrylate, polybutadiene acrylate, silicone acrylate, polyester acrylate, epoxy acrylate, and polyether acrylate. Among these, urethane acrylate resins are preferred, and those containing urethane acrylate oligomers containing at least one polyester polyol unit are particularly preferred. For example, the polyol component is polytetramethylene glycol (PTMG).
It is also preferable to use a polyester polyol of adipic acid and 1,6-hexanediol, in which the isocyanate component is isophorone diisocyanate (IPDI) and the acrylate component is 2-hydroxyethyl acrylate (HEA).
2次被覆の形成に用いる紫外線硬化性樹脂は、その硬化
物が25℃において1 、000〜20.00089
/ cdのヤング率を有するものであれば、従来の2次
被覆用の樹脂が使用でき、その具体例としては、たとえ
ばウレタンアクリレート系、エポキシアクリレート系、
ポリエステルアクリレ−ト系またはこられの混合系の紫
外線硬化性樹脂があげられる。The cured product of the ultraviolet curable resin used for forming the secondary coating has a molecular weight of 1,000 to 20.00089 at 25°C.
Conventional secondary coating resins can be used as long as they have a Young's modulus of /cd, and specific examples include urethane acrylate, epoxy acrylate,
Examples include UV-curable resins of polyester acrylate type or a mixture thereof.
本発明においては、1次被覆と2次被覆の間にバッファ
層を設けてもよい。バッファ層の形成に用いる樹脂とし
てはウレタンアクリレート系、シリコーンアクリレート
系、ポリブタジェンアクリレート系、ポリエーテルアク
リレート系、ポリエステルアクリレート系などの紫外線
硬化性樹脂が好適に用いられ、その硬化物のヤング率は
25℃で10〜1,000Kg/cd、好ましくは10
〜100Kg/cdであるのが適当である。In the present invention, a buffer layer may be provided between the primary coating and the secondary coating. As the resin used to form the buffer layer, ultraviolet curable resins such as urethane acrylate, silicone acrylate, polybutadiene acrylate, polyether acrylate, and polyester acrylate are preferably used, and the Young's modulus of the cured product is 10 to 1,000 Kg/cd at 25°C, preferably 10
~100Kg/cd is suitable.
1次被覆、バッファ層および2次被覆の厚さは光フアイ
バー心線構造などにより異なるが、それぞれ10〜20
0ρ、O〜300pおよび10〜SOO,の範囲で通常
選定される。The thickness of the primary coating, buffer layer, and secondary coating varies depending on the optical fiber core structure, etc., but each has a thickness of 10 to 20 mm.
It is usually selected in the ranges of 0 ρ, 0 to 300 p, and 10 to SOO.
かかる各紫外線硬化性樹脂は、各樹脂に適切な反応希釈
剤、光重合開始剤、顔料などを添加配合してワニスとさ
れる。反応希釈剤としては、たとえばHEA 、フェノ
キシエチルアクリレート、IPDI、フェニルジエチレ
ングリコールアクリレート、フェニルトリエチレングリ
コールアクリレート、ラウリルアクリレート、ペンタエ
リスリトールトリアクリレート、トリメチロールプロパ
ントリアクリレート、ヘキサンジオールジアクリレート
、トリエテングリコールジアクリ ・)レート、ネオペ
ンチルグリコールジアクリレート、テトラエチレングリ
コールジアクリレート、N−ビニルピロリドン、2−エ
チルへキシルアクリレートなどがあげられ、光重合開始
剤としてはたとえば1−ヒドロキシシクロへキシルフェ
ニルケトン、ベンジルジメチルケタール、ベンゾフェノ
ン、ジェトキシアセトフェノン、2−ヒドロキシ−2−
メチル−1−フェニルプロペン−1−オン、イソブチル
ベンゾインエーテル、イソプロピルベンゾインエーテル
、ヒドロキシシクロへキシルフェニルケトンなどがあげ
られるが、これらのみに限定されるものではない。Each of these ultraviolet curable resins is made into a varnish by adding and blending an appropriate reaction diluent, photopolymerization initiator, pigment, etc. to each resin. Examples of reaction diluents include HEA, phenoxyethyl acrylate, IPDI, phenyldiethylene glycol acrylate, phenyltriethylene glycol acrylate, lauryl acrylate, pentaerythritol triacrylate, trimethylolpropane triacrylate, hexanediol diacrylate, triethene glycol diacrylate. ), neopentyl glycol diacrylate, tetraethylene glycol diacrylate, N-vinylpyrrolidone, 2-ethylhexyl acrylate, etc., and photopolymerization initiators include, for example, 1-hydroxycyclohexylphenyl ketone, benzyl dimethyl ketal. , benzophenone, jetoxyacetophenone, 2-hydroxy-2-
Examples include, but are not limited to, methyl-1-phenylpropen-1-one, isobutylbenzoin ether, isopropylbenzoin ether, and hydroxycyclohexylphenyl ketone.
1次被覆の形成方法としては種々の方法が採用されるが
、たとえば石英ガラス系光フアイバー母材を溶融線引き
した光ファイバーを1次被覆用ワニス中を通して塗布し
たのち紫外線を照射して硬化させ、ついで同様にバッフ
ァ層用ワニスの塗布・硬化および2次被覆用ワニスの塗
布・硬化を行なう方法があげられる。塗布条件や硬化条
件は用いる樹脂の種類、塗布厚、線速などにより適宜選
定すればよい。Various methods are used to form the primary coating. For example, an optical fiber made by melting and drawing a quartz glass optical fiber base material is passed through a varnish for the primary coating, and then cured by irradiation with ultraviolet rays. Similarly, there is a method of applying and curing a varnish for a buffer layer and a method of applying and curing a varnish for a secondary coating. Coating conditions and curing conditions may be appropriately selected depending on the type of resin used, coating thickness, line speed, etc.
本発明の樹脂被覆用光ファイバーは第1図に示すような
1g線型光フアイバーに適用してもよいし、第2図に示
すごとくテープ型光ファイバーに適用してもよい。The resin-coated optical fiber of the present invention may be applied to a 1g linear optical fiber as shown in FIG. 1, or a tape-type optical fiber as shown in FIG.
第1図において、(1)は光ファイバーであり、その直
上に1法被m(2)が設けられ、バッファ的(4)を介
して2次被覆(3)が設けられている。第2図に示され
るテープ型光ファイバーは、光ファイバー(1)上に1
法被fi! (2) 、要すればバッファ層(図示され
ていない)、ついで2法被m (3]が設けられた単線
型の光フアイバー素線(5)を数本束ね、それらの周囲
にテープ被覆IJ (61を設けたものである。テープ
被I W4(6]の拐料としては、たとえばウレタンア
クリレート系、ポリエステルアクリレート系、エポキシ
アクリレート系などの紫外線硬化性樹脂またはそれらの
混合物などが用いられる。In FIG. 1, (1) is an optical fiber, a first optical fiber (2) is provided directly above it, and a secondary coating (3) is provided via a buffer (4). The tape-type optical fiber shown in Figure 2 has one
Happi coat fi! (2) If necessary, a buffer layer (not shown) and then two optical fibers (3) are bundled together. (61 is provided.) As the coating agent for the tape IW4 (6), for example, an ultraviolet curable resin such as urethane acrylate, polyester acrylate, or epoxy acrylate, or a mixture thereof is used.
つぎに本発明の樹脂被覆光ファイバーを実施例に基づい
て説明するが、本発明はかかる実施例のみに限定される
ものではない。Next, the resin-coated optical fiber of the present invention will be explained based on Examples, but the present invention is not limited to these Examples.
実施例1
ポリオール成分(PTHG+アジピン酸と1.6−ヘキ
サンジオールのポリエステルポリオール)とイソアネー
ト成分(IPDI)とアクリレート成分(IIεA)と
からなるウレタンアクリレート系紫外線硬化性樹脂(大
日本インキ化学工業■製のグランディックFG70G)
を1次被覆材として用い、また2次被覆材としてPTH
Gとトリレンジイソシアネート(TDI)とHEAとか
らなるウレタンアクリレートおよびビスフェノールA・
エピクロルヒドリンとアクリル酸とからなるエポキシア
クリレートとの混合物(日本合成ゴム(t[、デソライ
ト950Y100)を用いた。Example 1 Urethane acrylate-based ultraviolet curable resin (manufactured by Dainippon Ink & Chemicals) consisting of a polyol component (PTHG + polyester polyol of adipic acid and 1,6-hexanediol), an isoanate component (IPDI), and an acrylate component (IIεA) Grandic FG70G)
was used as the primary coating material, and PTH was used as the secondary coating material.
Urethane acrylate consisting of G, tolylene diisocyanate (TDI) and HEA, and bisphenol A.
A mixture of epoxy acrylate consisting of epichlorohydrin and acrylic acid (Japan Synthetic Rubber (t[, Desolite 950Y100) was used.
VAD法で作製したGl型石英ガラス系光ファイバー母
材を線引き速度30m/分で線引きし、えられた光ファ
イバー(直径12hm)と同速度で前記1次被覆用ワニ
スが溜められているポット中を通して1次被覆材ワニス
を塗布し、ついで有効長さ50αの紫外線照射装置を通
して硬化させ(有効照射時間1秒) 、90遍厚の1次
被覆を形成した。A Gl-type quartz glass optical fiber base material prepared by the VAD method was drawn at a drawing speed of 30 m/min, and passed through a pot containing the primary coating varnish at the same speed as the obtained optical fiber (diameter 12 hm). The next coating material varnish was applied and then cured through an ultraviolet irradiation device with an effective length of 50α (effective irradiation time: 1 second) to form a primary coating with a thickness of 90 mm.
つづいて、2次被覆用ワニスの塗布、紫外線照射(有効
照射時間1秒)をして300ρ厚の2次>1L faを
形成し、本発明の樹脂被覆光ファイバーを作製した。Subsequently, a secondary coating varnish was applied and ultraviolet rays were irradiated (effective irradiation time: 1 second) to form a secondary >1L fa having a thickness of 300ρ, thereby producing a resin-coated optical fiber of the present invention.
各被覆層のAヤング率はそれぞれつきのとおりであった
。The A Young's modulus of each coating layer was as shown below.
1次被覆 :25℃で75に97dl
−30℃で2,200に9/l:d
2次法被 : 25℃で5.0OOK!F / C
d−30℃で8,400Ky/cd
ヤング率の測定は、使用ワニスを約150」厚のフィル
ム状に成形し、充分に紫外線を照射して硬化させ、幅1
5.のタンザク状サンプルを作製し、このサンプルを引
張速ri11 m /分で引張試験を行なったときの伸
び2.5%時点での引張弾性率をヤング率とした。Primary coating: 75 to 97 dl at 25℃ 2,200 to 9/l:d at -30℃ Secondary coat: 5.0OOK at 25℃! F/C
8,400 Ky/cd at -30°C Young's modulus is measured by molding the varnish used into a film with a thickness of about 150", curing it by sufficiently irradiating it with ultraviolet rays, and making a film with a width of 1
5. A tanzak-shaped sample was prepared, and this sample was subjected to a tensile test at a tensile rate of 11 m/min, and the tensile modulus at an elongation of 2.5% was taken as Young's modulus.
えられた樹脂被覆光ファイバーを約30 cmの束取り
状態とし、恒温槽に入れて波長1.30 Jlで・)の
伝送損失を測定したところ、25℃での伝送損失は0.
50dB/kmであり、−30℃での伝送損失は0.5
5dB/ka+であって、その伝送損失増加繕は0、0
5dB/に+aに抑えられた。The resulting resin-coated optical fibers were bundled into a bundle of about 30 cm, placed in a thermostatic oven, and measured for transmission loss at a wavelength of 1.30 Jl. The transmission loss at 25°C was 0.
50dB/km, transmission loss at -30℃ is 0.5
5dB/ka+, and its transmission loss increase is 0.0.
It was suppressed to 5dB/+a.
比較例1
1次被覆材としてPTHGとIPDIと11[Aとから
なるウレタンアクリレート(大日本インキ化学工業■製
のグランディックFC70g 、25℃および一30℃
でのヤング率はいずれも38Kf/7)を用いたほかは
実施例1と同様にして紫外線硬化樹脂被覆光ファイバー
を作製し、実施例1と同様にして伝送損失を測定したと
ころ、25℃で0.50dB/1v1−30℃で3.0
dB/に+a t’あった(損失増加量: 2.5d
B/km )。Comparative Example 1 Urethane acrylate consisting of PTHG, IPDI, and 11[A] (Grandic FC70 g manufactured by Dainippon Ink & Chemicals, 25°C and -30°C) was used as the primary coating material.
An optical fiber coated with an ultraviolet curable resin was prepared in the same manner as in Example 1 except that Young's modulus at 38 Kf/7) was used, and the transmission loss was measured in the same manner as in Example 1. .50dB/1v1-3.0 at 30℃
There was +a t' in dB/ (loss increase amount: 2.5d
B/km).
比較例2
1次被覆材としてウレタンアクリレート系紫外&lI化
樹脂(デッド社製のデソライト950x065.25℃
および一30℃でのヤング率はそれぞれ25に9/−お
よび30.000Kg/ cd )を用いたほかは実施
例1と同様にして紫外線硬化樹脂被覆光ファイバーを作
製し、実施例1と同様にして伝送損失を測定したところ
、25℃で0.50dB/km1−30℃で20.5d
B/kn+であった(損失増加m:20、OdB/km
)。Comparative Example 2 As the primary coating material, urethane acrylate-based ultraviolet & II resin (Desolite 950x065.25°C manufactured by Dead Co., Ltd.) was used as the primary coating material.
An optical fiber coated with an ultraviolet curing resin was prepared in the same manner as in Example 1, except that the Young's modulus at -30°C was 25, 9/- and 30.000 Kg/cd, respectively. When the transmission loss was measured, it was 0.50dB/km at 25℃ and 20.5d at 30℃.
B/kn+ (loss increase m: 20, OdB/km
).
実施例2
1次被覆としてアジピン酸エチレングリコールとTOI
とI E Aとからなる。ウレタンアクリレート(三菱
油化ファイン@製の0GEI、25℃および一30℃で
のヤング率はそれぞれ22に9/ctAおよび13、
ooo*g/ m )を用いたほかは実施例1と同様に
して紫外線硬化樹脂被覆光ファイバーを作製し、実施例
1と同様にして伝送損失を測定したところ、25℃で0
.50dB/km、 −30℃−(−0,f35dB
/killであった(損失増加ffl : 0.15
dB/km)。Example 2 Ethylene glycol adipate and TOI as primary coating
and IEA. Urethane acrylate (0GEI manufactured by Mitsubishi Yuka Fine@, Young's modulus at 25°C and -30°C is 22 to 9/ctA and 13, respectively)
An optical fiber coated with an ultraviolet curable resin was prepared in the same manner as in Example 1 except that 0.00 * g/m ) was used, and the transmission loss was measured in the same manner as in Example 1.
.. 50dB/km, -30℃-(-0, f35dB
/kill (loss increaseffl: 0.15
dB/km).
実施例3
1次被覆の厚さを200Al111および2次被覆の厚
さを300項としたほかは実施例1と同じ樹脂を用いて
1次、2次被覆を有する樹脂被覆光ファイバー素線を作
製した。Example 3 A resin-coated optical fiber strand having primary and secondary coatings was produced using the same resin as in Example 1, except that the thickness of the primary coating was 200Al111 and the thickness of the secondary coating was 300 items. .
この光フアイバー索線を5本並べてデソライト950Y
100を用いて一括被覆し、紫外線を照射して硬化させ
てテープ型光ファイバー心線(0,45amX 1.
6m>を作製した。Five of these optical fiber cables are lined up and made into Desolite 950Y.
100 and cured by irradiating with ultraviolet rays to form a tape-type optical fiber core (0.45 am x 1.
6m> was produced.
えられたテープ型心線の伝送損失を実施例1と同様にし
て測定したところ、25℃では0.50dB/lvであ
り、−30℃に下げても損失量は変化しなかった。When the transmission loss of the obtained tape-shaped core wire was measured in the same manner as in Example 1, it was 0.50 dB/lv at 25°C, and the loss did not change even when the temperature was lowered to -30°C.
[発明の効果]
本発明によれば、低温時においても低いヤング率のもの
でなければ低温での光伝送損失が大きくなるという従来
の常識を打ち破った光伝送特性の優れた樹脂面光ファイ
バーを提供することができる。[Effects of the Invention] According to the present invention, a resin-faced optical fiber with excellent optical transmission characteristics is provided, which breaks the conventional wisdom that unless the Young's modulus is low even at low temperatures, the optical transmission loss will be large at low temperatures. can do.
4、面の簡単な説明
第1図は本発明の樹脂被覆光ファイバーの単線型の一実
施例の概略断面図、第2図は本発明の樹脂被覆光ファイ
バーのテープ型の一実施例の概略断面図である。4. Brief description of aspects Fig. 1 is a schematic cross-sectional view of an embodiment of the resin-coated optical fiber of the single wire type of the present invention, and Fig. 2 is a schematic cross-sectional view of an embodiment of the tape-type resin-coated optical fiber of the present invention. It is.
(図面の主要符号) (1):光ファイバー (21: 1次被覆 (31: 2次被覆 71 図 72図(Main symbols on drawings) (1): Optical fiber (21: Primary coating (31: Secondary coating 71 Figure Figure 72
Claims (1)
2次被覆が形成されている石英ガラス系光ファイバーで
あって、1次被覆の紫外線硬化物が25℃および−30
℃でそれぞれ10〜100kg/cm^2および100
〜20,000kg/cm^2のヤング率を有し、かつ
2次被覆の紫外線硬化物が25℃で1,000〜20,
000kg/cm^2のヤング率を有する紫外線硬化樹
脂被覆光ファイバー。 2 1次被覆用紫外線硬化性樹脂が、ポリエステルポリ
オール単位を少なくとも1個含むウレタンアクリレート
オリゴマーを含有している特許請求の範囲第1項記載の
光ファイバー。 3 単線型光ファイバーである特許請求の範囲第1項ま
たは第2項記載の光ファイバー。 4 テープ型光ファイバーである特許請求の範囲第1項
または第2項記載の光ファイバー。[Scope of Claims] 1. A silica glass optical fiber having a primary coating and a secondary coating formed of an ultraviolet cured product of an ultraviolet curable resin, wherein the ultraviolet cured product of the primary coating is heated at 25°C and -30°C.
10-100 kg/cm^2 and 100 respectively at °C
It has a Young's modulus of ~20,000 kg/cm^2, and the UV-cured material of the secondary coating has a Young's modulus of 1,000~20 at 25°C.
An ultraviolet curing resin coated optical fiber with a Young's modulus of 000 kg/cm^2. 2. The optical fiber according to claim 1, wherein the ultraviolet curable resin for primary coating contains a urethane acrylate oligomer containing at least one polyester polyol unit. 3. The optical fiber according to claim 1 or 2, which is a single-wire optical fiber. 4. The optical fiber according to claim 1 or 2, which is a tape-type optical fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61012870A JP2660278B2 (en) | 1986-01-23 | 1986-01-23 | UV cured resin coated optical fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61012870A JP2660278B2 (en) | 1986-01-23 | 1986-01-23 | UV cured resin coated optical fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62170920A true JPS62170920A (en) | 1987-07-28 |
JP2660278B2 JP2660278B2 (en) | 1997-10-08 |
Family
ID=11817453
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61012870A Expired - Lifetime JP2660278B2 (en) | 1986-01-23 | 1986-01-23 | UV cured resin coated optical fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2660278B2 (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60254010A (en) * | 1984-05-23 | 1985-12-14 | Sumitomo Electric Ind Ltd | Fiber for optical transmission |
-
1986
- 1986-01-23 JP JP61012870A patent/JP2660278B2/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60254010A (en) * | 1984-05-23 | 1985-12-14 | Sumitomo Electric Ind Ltd | Fiber for optical transmission |
Also Published As
Publication number | Publication date |
---|---|
JP2660278B2 (en) | 1997-10-08 |
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