JPS6257582B2 - - Google Patents
Info
- Publication number
- JPS6257582B2 JPS6257582B2 JP57086174A JP8617482A JPS6257582B2 JP S6257582 B2 JPS6257582 B2 JP S6257582B2 JP 57086174 A JP57086174 A JP 57086174A JP 8617482 A JP8617482 A JP 8617482A JP S6257582 B2 JPS6257582 B2 JP S6257582B2
- Authority
- JP
- Japan
- Prior art keywords
- glass fiber
- coated
- coating
- cured
- coating layer
- 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.)
- Expired
Links
- 239000003365 glass fiber Substances 0.000 claims description 22
- 230000005540 biological transmission Effects 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 239000011247 coating layer Substances 0.000 claims description 6
- 229920001296 polysiloxane Polymers 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- -1 polysiloxane Polymers 0.000 claims description 5
- 230000001678 irradiating effect Effects 0.000 claims 1
- 230000003287 optical effect Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- MSAHTMIQULFMRG-UHFFFAOYSA-N 1,2-diphenyl-2-propan-2-yloxyethanone Chemical compound C=1C=CC=CC=1C(OC(C)C)C(=O)C1=CC=CC=C1 MSAHTMIQULFMRG-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 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
- 229910000085 borane Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明は光伝送用ガラスフアイバに係り、特に
ガラスフアイバ表面に保護用の硬化被覆層を設け
る光伝送用ガラスフアイバの製造法に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a glass fiber for light transmission, and more particularly to a method for manufacturing a glass fiber for light transmission in which a protective hardened coating layer is provided on the surface of the glass fiber.
光伝送用ガラスフアイバには主として石英ガラ
スが使用されている。しかし、ガラスフアイバ表
面に微小な欠陥があると、機械的強度が著しく低
下し実用できなくなる。そのため、ガラスフアイ
バ表面に液状のゴムや樹脂を塗布し、電気炉等に
よつて焼付けて保護被覆を形成させることが行な
われている。この方法は、保護被覆の硬化速度が
おそいため生産性をあげるには大きな設備を必要
としていた。また、硬化速度を高めるには当然反
応性の大きい組成にする必要があるがこのような
被覆組成物は、ガラスフアイバの線引き直後に被
覆されるため、まず十分に冷却しきれない石英ガ
ラスに接触することによつて、ただちに硬化現象
を起こし、ガラスフアイバ表面の微小欠陥を埋め
るという所定の目的が達成されない可能性があ
る。また、反応性を小さくし、ポツトライフを長
くすると硬化速度が低下するため製造上の難点と
なつていた。 Silica glass is mainly used for optical transmission glass fibers. However, if there are minute defects on the surface of the glass fiber, the mechanical strength will be significantly reduced, making it impractical. Therefore, a protective coating is formed by applying liquid rubber or resin to the surface of the glass fiber and baking it in an electric furnace or the like. This method requires large equipment to increase productivity because the protective coating has a slow curing speed. Additionally, in order to increase the curing speed, it is naturally necessary to use a highly reactive composition, but since such a coating composition is coated immediately after drawing the glass fiber, it first comes into contact with the quartz glass, which has not yet been sufficiently cooled. By doing so, a hardening phenomenon may occur immediately, and the intended purpose of filling micro defects on the surface of the glass fiber may not be achieved. Furthermore, if the reactivity is reduced and the pot life is lengthened, the curing speed decreases, which is a problem in manufacturing.
本発明の目的は、上記難点を解消し、ガラスフ
アイバ表面に、保護用の硬化被覆層を高速度に形
成させることができる光伝送用ガラスフアイバの
製造法を提供することにある。 SUMMARY OF THE INVENTION An object of the present invention is to provide a method for manufacturing a glass fiber for optical transmission, which eliminates the above-mentioned difficulties and allows a protective cured coating layer to be formed on the surface of the glass fiber at high speed.
本発明は、ガラスフアイバ表面に、分子中にC
=C二重結合を有するポリシロキサンと分子中に
SH基を有するオルガノポリシロキサンとの混合
物を主体とする光硬化性組成物を被覆し、かつ紫
外線を照射して硬化被覆層を形成させることを特
徴とするものである。 The present invention provides C in molecules on the surface of a glass fiber.
Polysiloxane with =C double bond and in the molecule
It is characterized in that it is coated with a photocurable composition mainly consisting of a mixture with an organopolysiloxane having an SH group, and is irradiated with ultraviolet rays to form a cured coating layer.
この光伝送用ガラスフアイバの製造法における
光硬化性組成物とは、上述の二混合物を主体と
し、これに光増感剤を混合したもので、光増感剤
としては、ベンゾフエノン、ベンゾイン、ベンゾ
インエチルエーテル、ベンゾインイソプロピルエ
ーテル、2,2−ジエトキシアセトフエノン、ベ
ンジルジメチルケタール、チオキサントン、アン
トラキノン等が該当するがこれらに限定されるも
のではない。 The photocurable composition used in this method for producing a glass fiber for optical transmission is mainly composed of the above-mentioned two mixtures, with a photosensitizer mixed therein. Examples include, but are not limited to, ethyl ether, benzoin isopropyl ether, 2,2-diethoxyacetophenone, benzyl dimethyl ketal, thioxanthone, anthraquinone, and the like.
また、その他反応性希釈剤、モノマ、重合防止
剤、顔料染料等の着色剤、接着剤、平滑性付与
剤、充填剤、帯電防止剤等、必要に応じて粘度調
整用の有機溶剤を含んでいても差支えない。 In addition, other reactive diluents, monomers, polymerization inhibitors, coloring agents such as pigment dyes, adhesives, smoothing agents, fillers, antistatic agents, etc., and organic solvents for viscosity adjustment as necessary. There is no problem even if there is.
これらの組成物を均一に混合したものを、ガラ
スフアイバの表面に被覆する。被覆する方法とし
ては、塗布、押出等でよく、またこれらの方法に
限定されるものではない。 A uniform mixture of these compositions is coated on the surface of the glass fiber. The coating method may be coating, extrusion, etc., and is not limited to these methods.
次に、被覆されたガラスフアイバは、他の固形
物に触れる前に紫外線硬化装置を通過させ、紫外
線を照射して硬化させる。この硬化操作は、1回
で行なつてもよく、また、表面が固形物に触れて
も粘着しない程度に半硬化させ、次工程で完全に
硬化させてもよい。 The coated glass fiber is then passed through an ultraviolet curing device and cured with ultraviolet light before contacting other solid objects. This curing operation may be performed at one time, or the surface may be semi-cured to such an extent that it does not stick even when it comes into contact with a solid substance, and then completely cured in the next step.
このようにして製造した光伝送用フアイバは、
そのまま巻取つてもよいし、巻取る前に、別途バ
ツフア層と補強層との被覆を施してもよい。 The optical transmission fiber manufactured in this way is
It may be wound up as is, or it may be coated with a buffer layer and a reinforcing layer separately before winding up.
なお、ガラスフアイバ表面に光硬化性組成物を
被覆する際に、ガラスフアイバ表面に、プライマ
シランカツプリング剤、チタネートカツプリング
剤、ボラン処理等を施し、接着力を向上させるこ
ともできる。 Note that when coating the glass fiber surface with the photocurable composition, the glass fiber surface can be treated with a primer silane coupling agent, a titanate coupling agent, a borane treatment, etc. to improve the adhesive strength.
以下に本発明の具体的実施例により説明する。 The present invention will be explained below using specific examples.
実施例 1
外径125μの光伝送用石英ガラスフアイバ表面
にC=C二重結合を有するポリシロキサン50重量
部、SH基を有するオルガノポリシロキサン50重
量部、ベンゾフエノン3重量部を均一になるまで
混合した組成物を厚さ20μになるよう塗布し、こ
れに、高圧水銀灯(80W/cm、照射距離10cm)を
用い、ライン速度50m/mmで紫外線硬化させた。
これをインストロン引張試験機を用い、20℃、引
張り速さ5mm/mm、チヤツク間距離50mmで引張試
験を行なつた結果、引張破断荷重は6Kgであつ
た。また、ポリアミド樹脂を2次被覆したもの
(外径0.9mm)の耐マイクロベンド性は良好で、伝
送特性の変化は認められなかつた。Example 1 50 parts by weight of polysiloxane having a C=C double bond, 50 parts by weight of organopolysiloxane having an SH group, and 3 parts by weight of benzophenone were mixed on the surface of a quartz glass fiber for optical transmission with an outer diameter of 125μ until uniform. The resulting composition was applied to a thickness of 20 μm, and cured with ultraviolet light using a high-pressure mercury lamp (80 W/cm, irradiation distance 10 cm) at a line speed of 50 m/mm.
This was subjected to a tensile test using an Instron tensile testing machine at 20°C, a tensile speed of 5 mm/mm, and a distance between chucks of 50 mm, and the tensile breaking load was 6 kg. Furthermore, the microbending resistance of the secondary coating with polyamide resin (outer diameter 0.9 mm) was good, and no change in transmission characteristics was observed.
実施例 2
実施例1と同じ組成を外径125μの光伝送用石
英ガラスフアイバに厚さ100μに押出被覆し、実
施例1と同様に引張試験を行なつた結果、引張破
断荷重は5Kgであつた。また、ポリフツ化ビニリ
デン樹脂を2次被覆したもの(外径0.9mm)の耐
マイクロベンド性は良好で、伝送特性の変化は認
められなかつた。Example 2 A quartz glass fiber for optical transmission with the same composition as in Example 1 was extruded and coated to a thickness of 100 μm with an outer diameter of 125 μm, and a tensile test was conducted in the same manner as in Example 1. As a result, the tensile breaking load was 5 kg. Ta. Furthermore, the microbending resistance of the secondary coating of polyvinylidene fluoride resin (outer diameter 0.9 mm) was good, and no change in transmission characteristics was observed.
これら実施例1、実施例2に用いた石英ガラス
フアイバそのままの引張破断荷重は1Kg以下で極
めて弱く、ケーブル化が困難であつた。 The tensile breaking load of the silica glass fibers used in Examples 1 and 2 was extremely weak, less than 1 kg, and it was difficult to make them into cables.
以上説明したように、本発明によれば、ポツト
ライフが長く、可撓性が良好で耐熱性にすぐれ、
かつ、接着性の良好な硬化被覆層を高速に施すこ
とができ、被覆層の形成には従来同様液状樹脂を
塗布または押出し被覆が可能であり、さらに、着
色も自由である等、すぐれた光伝送用ガラスフア
イバを容易に製造し得るという実用的効果を奏す
ることができる。 As explained above, according to the present invention, the pot life is long, the flexibility is good, the heat resistance is excellent,
In addition, a cured coating layer with good adhesion can be applied at high speed, and the coating layer can be formed by applying or extruding liquid resin in the same way as conventional methods.Furthermore, it can be colored freely, and has excellent optical properties. A practical effect can be achieved in that a glass fiber for transmission can be easily manufactured.
Claims (1)
結合を有するポリシロキサンと分子中にSH基を
有するオルガノポリシロキサンとの混合物を主体
とする光硬化性組成物を被覆し、かつ、紫外線を
照射して硬化被覆層を形成させることを特徴とす
る光伝送用ガラスフアイバの製造法。1 The surface of the glass fiber is coated with a photocurable composition mainly consisting of a mixture of polysiloxane having a C=C double bond in the molecule and organopolysiloxane having an SH group in the molecule, and is exposed to ultraviolet rays. A method for producing a glass fiber for light transmission, comprising irradiating it to form a cured coating layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57086174A JPS58204845A (en) | 1982-05-21 | 1982-05-21 | Manufacture of glass fiber for light transmission |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57086174A JPS58204845A (en) | 1982-05-21 | 1982-05-21 | Manufacture of glass fiber for light transmission |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58204845A JPS58204845A (en) | 1983-11-29 |
| JPS6257582B2 true JPS6257582B2 (en) | 1987-12-01 |
Family
ID=13879389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57086174A Granted JPS58204845A (en) | 1982-05-21 | 1982-05-21 | Manufacture of glass fiber for light transmission |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58204845A (en) |
-
1982
- 1982-05-21 JP JP57086174A patent/JPS58204845A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58204845A (en) | 1983-11-29 |
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