JPH0224771B2 - - Google Patents
Info
- Publication number
- JPH0224771B2 JPH0224771B2 JP19801881A JP19801881A JPH0224771B2 JP H0224771 B2 JPH0224771 B2 JP H0224771B2 JP 19801881 A JP19801881 A JP 19801881A JP 19801881 A JP19801881 A JP 19801881A JP H0224771 B2 JPH0224771 B2 JP H0224771B2
- Authority
- JP
- Japan
- Prior art keywords
- organic polymer
- fibers
- multiple fibers
- polymer layer
- drawn
- 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 - Lifetime
Links
- 239000000835 fiber Substances 0.000 claims description 38
- 229920000620 organic polymer Polymers 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
- 239000013307 optical fiber Substances 0.000 claims description 18
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 230000003287 optical effect Effects 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- 238000011437 continuous method Methods 0.000 claims 1
- 239000010410 layer Substances 0.000 description 23
- 239000002966 varnish Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 235000012239 silicon dioxide Nutrition 0.000 description 5
- 239000010453 quartz Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- 238000005491 wire drawing Methods 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000002052 molecular layer Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/104—Coating to obtain optical fibres
- C03C25/106—Single coatings
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
- C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
- C04B2237/32—Ceramic
- C04B2237/36—Non-oxidic
- C04B2237/366—Aluminium nitride
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Manufacture, Treatment Of Glass Fibers (AREA)
Description
【発明の詳細な説明】
本発明は、イメージガイドの画像伝送線路とし
て好適の光学用石英ガラス系マルチプルフアイバ
の連続製法に関する。
マルチプルフアイバは、従来から、所謂シング
ルフアイバ・ワインデング法により配列製造され
て来ているが、この方法は、極めて非能率である
のでマルチプルフアイバのコストアツプの大きな
要因となつている。更に、近時、低ロスの石英ガ
ラス系光フアイバの開発により、該フアイバから
なるマルチプルフアイバは、数十mもの長尺にお
いても画像伝送が可能と考えられているが、前記
従来法では長尺のものの製造が実質不可能のた
め、折角の石英ガラス系マルチプルフアイバの長
所が活し得ない欠点がある。
本発明者らは、先に石英系光フアイバ素線の多
数本からなる束を線引きするマルチプルフアイバ
の製法を開発した。ところでこの製法を連続化す
るためには、線引きされたマルチプルフアイバを
ドラムに巻取る必要があるが、外径が1mm以上の
太いマルチプルフアイバの場合は、石英ガラスに
特有の剛直性の故にドラム巻きができず、あえ
て、ドラム巻きを行うとマルチプルフアイバが破
断する問題がある。
石英ガラス系光フアイバの製造において、それ
らフアイバの可撓性や強度を改善するために線引
直後のフアイバの上に20μm以下程度の極く薄層
の有機高分子の層を形成する技術が公知である
(たとえば、特公昭56−19296号、特公昭55−
30201号参照)。本発明者らの研究によれば、1本
の石英系光フアイバ母材を線引きし、それにて得
られる細い光フアイバの可撓性などの改善には、
上記の極く薄い有機高分子層の形成にて充分効果
があるが、石英系光フアイバ母材あるいは該母材
を線引きして得た光フアイバの多数本、たとえば
数十本〜数千本、場合によつては数万本を束ねた
ものを線引きして外径1mm以上の太いマルチプル
フアイバを製造する場合、線引きによつて得られ
た上記マルチプルフアイバに、上記した如き薄層
の有機高分子層を形成しても、実際上マルチプル
フアイバの可撓性等を改善することはできない。
その理由は、種々あるが、次に述べる理由が主
なものである。
即ち、光フアイバの製造の場合は、線引きの対
象となるのは一本の母材であるため、線引きの芯
出しが容易であり、従つて線引された光フアイバ
上への薄肉の有機高分子層を均一に施こすことも
容易であるが、マルチプルフアイバの製造におい
ては、線引きの対象となるのは、多数本の光フア
イバ又はその母材(以下それらを光フアイバ素線
と称す)の束又は該束を収容した石英ガラス製の
スキンパイプである。上記の束に含まれる光フア
イバ素線がいかに均質よく製造されたものであつ
ても、光フアイバ製造の場合の線引き対象となる
ただ1本の光フアイバ母材と比較して上記束又は
該束を収容せるスキンパイプは、断面における均
質性において、光フアイバ製造の場合のただ1本
の光フアイバ母材のそれと比較して格段に劣る。
即ち不均質である。この不均質性の故に線引きに
おいて芯出しが容易でなく、かつまた線引きされ
たものの断面が異形化し易い。線引き後の外径が
1mm以上の太物である場合は、特にこの傾向が強
い。線引き時の芯出し不良や線引きされたものの
断面の異形化は、いずれも均一薄肉の有機高分子
層の形成を困難にする。
本発明は、上記の問題の解決された外径1〜5
mmの光学用石英ガラス系マルチプルフアイバの連
続製法を提案するものであつて、線引きされたマ
ルチプルフアイバの上に塗料塗布により厚さ
100μm以上、伸び3%以上、引張弾性率1000
Kg/cm2以上の密着有機高分子層を形成することを
特徴とするものである。
本発明において、製造対象とするマルチプルフ
アイバの外径を1〜5mmと限定する理由は、1mm
未満の細いマルチプルフアイバでは、光フアイバ
の連続製造において公知の薄肉有機高分子層の施
与により、マルチプルフアイバの可撓性が改善さ
れ得るからであり、一方、外径5mmより大の太い
マルチプルフアイバでは、たとえ厚肉の有機高分
子層を施しても可撓性の改善が左程達成されない
からである。また、マルチプルフアイバに施され
た有機高分子層の物性を上記の通りに限定する理
由は、上記物性を満足しない有機高分子層は、た
とえ100μm以上の厚肉であつてもマルチプルフ
アイバの可撓性を改善する効果が乏しいためであ
る。
マルチプルフアイバ上の有機高分子層は、マル
チプルフアイバと良好に密着していることが肝要
であり、実際的には、製造時におけるドラム巻又
はそれと同程度の屈曲を受けても剥離しない程度
以上でなければならない。次に述べる方法で測定
した剥離強度が50g/mm以上であるものは、上記
の密着要求を満足し得る。
剥離強度:固形分、油脂分、水分などを充分に
除去した表面清浄な幅20〜30mmのガラス板上に有
機高分子層を塗布乾燥又は塗布焼付により形成
し、剥離角度90度で該有機高分子層を剥離する。
上記の良好な密着は、有機高分子を、殊に極性
の有機高分子を塗布し、次いで乾燥固化又は照
射、焼付などの処理にて化学的に硬化させること
により達成される。殊に、有機高分子のワニスを
塗布し、次いで照射、焼付などの処理にて化学的
に硬化させることにより上記した物性を安定的に
満足する有機高分子層を形成し得る。なお、多く
の有機高分子ワニスは、焼付硬化時の高温度で一
時的に粘度低下し、このため硬化後の肉厚が所定
厚より薄くなる問題がある。従つて、かかる場合
には、可及的高粘度のワニスを用いる、あるいは
焼付を可及的低温度で行うなどの注意を要する。
その点、照射硬化し得るワニスは、硬化を低温度
で行えるので本発明の実施上、好適なものといえ
る。殊に室温での粘度が103〜5×104c.p.の紫外
線硬化形のものは特に好ましい。かかるワニスの
例としてはスリーボンド社のエポキシ―アクリル
系ワニス3031,3041,3051,W.R.グレース社製
のRCP―611HV,RCP―611などが例示できる。
なお、本発明において、マルチプルフアイバと
有機高分子層との可及的良好な密着を達成するた
めに、線引き直後の未だ表面汚染のない間に塗料
塗布を行つて有機高分子層を形成することが好ま
しく、更には重ね塗布にて100μm以上の層を形
成するよりも1回の塗布にて上記肉厚の施与を行
うことが好ましい。その理由は、重ね塗布を行う
と有機高分子層内に異物が混入し易く、異物の混
入がマルチプルフアイバの可撓性を低下せしめる
危険性が大きいからである。
以下、実施例、比較例により本発明を一層詳細
に説明する。
〔実施例1〜5、比較例1〜3〕
純石英ガラスからなる外径300μmのコア部の
外側にB2O3とFにてドープされた石英ガラスか
らなる厚さ35μmのクラツド層とさらにその上に
厚さ15μmの石英ガラスサポート層を有する外径
400μm、長さ40cmの光フアイバ素線11000本を20
容量%のフツ酸水溶液中で、ついで蒸溜水中でそ
れぞれ超音波を作用させて洗浄し、蒸溜水中で束
ねた。その素線束を内径48mm、外径51mmの合成石
英パイプ(スキンパイプ)中のほぼ中間に収納
し、次いで素線同士の密着を良好ならしめるため
に各素線の表面にB2O3を付着せしめて2000℃で
合成石英パイプごと線引きし、外径2.0mmのマル
チプルフアイバとした。線引き炉から出て、未だ
100℃以上の高温度状態にあるマルチプルフアイ
バの上に第1表に示す条件にて有機高分子層を形
成させた。同表には使用ワニス、形成された有機
高分子層の諸特性、並びに有機高分子層を有する
マルチプルフアイバの可撓性をまとめて示す。こ
のうち、可撓性は破断に至つたときのマルチプル
フアイバの屈曲半径(mm)で示す。なお、比較例
2,3及び実施例1〜5においては塗布ワニス
は、アイグラフイツク社製紫外線架橋装置
UB011―3A/Bを用い出力1000Wレベルで1〜
3秒程度の最適架橋条件にて紫外線照射して硬化
させた。
【表】DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for continuously manufacturing optical quartz glass multiple fibers suitable as image transmission lines for image guides. Conventionally, multiple fibers have been arrayed and manufactured by the so-called single fiber winding method, but this method is extremely inefficient and is a major factor in increasing the cost of multiple fibers. Furthermore, with the recent development of low-loss silica glass optical fibers, it is thought that multiple fibers made of these fibers can transmit images even over long lengths of several tens of meters. Since it is virtually impossible to manufacture quartz glass fibers, the advantages of quartz glass multiple fibers cannot be fully utilized. The present inventors previously developed a method for manufacturing multiple fibers in which a bundle consisting of a large number of silica-based optical fibers is drawn. By the way, in order to make this manufacturing method continuous, it is necessary to wind the drawn multiple fibers around a drum, but in the case of thick multiple fibers with an outer diameter of 1 mm or more, drum winding is necessary due to the rigidity unique to quartz glass. However, if drum winding is carried out, there is a problem that the multiple fibers may break. In the production of silica glass optical fibers, there is a well-known technique for forming an extremely thin organic polymer layer of approximately 20 μm or less on the fiber immediately after drawing in order to improve the flexibility and strength of the fiber. (For example, Special Publication No. 56-19296, Special Publication No. 55-
30201). According to the research conducted by the present inventors, in order to improve the flexibility of a thin optical fiber obtained by drawing a single quartz-based optical fiber base material,
Although the formation of the above-mentioned extremely thin organic polymer layer is sufficiently effective, a large number of quartz-based optical fibers or optical fibers obtained by drawing the base material, for example, tens to thousands of fibers, may be used. In some cases, when tens of thousands of fibers are drawn in a bundle to produce thick multiple fibers with an outer diameter of 1 mm or more, a thin layer of organic polymer as described above is added to the multiple fibers obtained by drawing. Even if layers are formed, the flexibility etc. of the multiple fiber cannot actually be improved. There are various reasons for this, but the following are the main reasons. In other words, in the case of manufacturing optical fibers, since the target of drawing is a single base material, centering of the drawing is easy, and therefore, it is easy to draw a thin organic layer onto the drawn optical fiber. Although it is easy to apply a uniform molecular layer, in the production of multiple fibers, the object of drawing is a large number of optical fibers or their base material (hereinafter referred to as optical fiber raw material). A bundle or a quartz glass skin pipe containing the bundle. No matter how homogeneous the optical fiber strands contained in the above bundle are, the bundle or the bundle may be compared with a single optical fiber base material to be drawn in the production of optical fibers. The homogeneity of the skin pipe containing the fiber in its cross section is significantly inferior to that of a single optical fiber base material in the case of optical fiber production.
That is, it is heterogeneous. Because of this non-uniformity, centering is not easy during wire drawing, and the cross section of the drawn wire tends to be irregular. This tendency is particularly strong when the wire is thick with an outer diameter of 1 mm or more after drawing. Poor centering during wire drawing and irregularly shaped cross sections of the drawn wire both make it difficult to form a uniformly thin organic polymer layer. The present invention solves the above problems and has an outer diameter of 1 to 5.
This paper proposes a continuous manufacturing method for quartz glass-based multiple fibers for optical use of mm in thickness.
100μm or more, elongation 3% or more, tensile modulus 1000
It is characterized by forming an adhesive organic polymer layer of Kg/cm 2 or more. In the present invention, the reason why the outer diameter of the multiple fiber to be manufactured is limited to 1 to 5 mm is 1 mm.
This is because, for multiple fibers with a diameter of less than This is because even if a thick organic polymer layer is applied, flexibility cannot be improved to the extent shown. In addition, the reason why the physical properties of the organic polymer layer applied to the multiple fibers are limited as described above is that the organic polymer layer that does not satisfy the above physical properties will not be flexible even if it is thicker than 100 μm. This is because it has little effect on improving sex. It is important that the organic polymer layer on the multiple fibers has good adhesion to the multiple fibers, and in practice, the organic polymer layer on the multiple fibers must be in good contact with the multiple fibers. There must be. Those having a peel strength of 50 g/mm or more as measured by the method described below can satisfy the above adhesion requirements. Peel strength: An organic polymer layer is formed by coating and drying or baking on a glass plate with a width of 20 to 30 mm whose surface has been sufficiently removed from solids, oil, fat, moisture, etc., and the organic polymer layer is peeled at a peeling angle of 90 degrees. Peel off the molecular layer. The above-mentioned good adhesion is achieved by applying an organic polymer, especially a polar organic polymer, and then chemically hardening it by drying, hardening, irradiation, baking, or other treatments. In particular, an organic polymer layer that stably satisfies the above physical properties can be formed by applying an organic polymer varnish and then chemically curing it through treatments such as irradiation and baking. Note that many organic polymer varnishes have a problem in that their viscosity temporarily decreases at high temperatures during bake-hardening, resulting in a wall thickness that becomes thinner than a predetermined thickness after hardening. Therefore, in such cases, care must be taken to use a varnish with as high a viscosity as possible or to perform baking at as low a temperature as possible.
In this respect, varnishes that can be cured by radiation are suitable for carrying out the present invention because they can be cured at low temperatures. Particularly preferred are UV-curable ones having a viscosity of 10 3 to 5×10 4 cp at room temperature. Examples of such varnishes include epoxy-acrylic varnishes 3031, 3041, and 3051 manufactured by ThreeBond, and RCP-611HV and RCP-611 manufactured by WR Grace. In the present invention, in order to achieve as good adhesion as possible between the multiple fibers and the organic polymer layer, the organic polymer layer is formed by applying paint while the surface is still free from contamination immediately after drawing. It is more preferable to apply the above-mentioned thickness in one application rather than to form a layer of 100 μm or more by multiple applications. The reason for this is that when multiple coatings are applied, foreign matter is likely to get mixed into the organic polymer layer, and there is a great risk that foreign matter will reduce the flexibility of the multiple fibers. Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. [Examples 1 to 5, Comparative Examples 1 to 3] A cladding layer with a thickness of 35 μm made of quartz glass doped with B 2 O 3 and F on the outside of the core portion made of pure silica glass and having an outer diameter of 300 μm, and further Outer diameter with a 15μm thick quartz glass support layer on top of it
20 pieces of 11,000 optical fibers with a length of 400μm and a length of 40cm
They were washed in a hydrofluoric acid aqueous solution of % by volume and then in distilled water by applying ultrasonic waves, and bundled in distilled water. The bundle of strands was stored approximately in the middle of a synthetic quartz pipe (skin pipe) with an inner diameter of 48 mm and an outer diameter of 51 mm, and then B 2 O 3 was attached to the surface of each strand to ensure good adhesion between the strands. At least the synthetic quartz pipe was drawn at 2000℃ to create multiple fibers with an outer diameter of 2.0mm. Out of the wire drawing furnace, still
An organic polymer layer was formed on the multiple fibers at a high temperature of 100° C. or higher under the conditions shown in Table 1. The table summarizes the varnish used, various properties of the organic polymer layer formed, and the flexibility of the multiple fibers having the organic polymer layer. Among these, flexibility is expressed as the bending radius (mm) of the multiple fiber when it breaks. In addition, in Comparative Examples 2 and 3 and Examples 1 to 5, the applied varnish was made using an ultraviolet crosslinking device manufactured by Igraphik Co., Ltd.
1~ at output 1000W level using UB011-3A/B
It was cured by irradiating ultraviolet rays under optimal crosslinking conditions for about 3 seconds. 【table】
Claims (1)
る束を線引きして外径1〜5mmのマルチプルフア
イバとし、線引きされたマルチプルフアイバの上
に、塗料塗布により厚さ100μm以上、伸び3%
以上、引張弾性率1000Kg/cm2以上の密着有機高分
子層を形成することを特徴とする光学用石英ガラ
ス系マルチプルフアイバの連続製法。 2 密着有機高分子層を、マルチプルフアイバの
線引き直後に、かつ一回の塗料塗布により形成す
ることを特徴とする特許請求の範囲第1項の連続
製法。[Scope of Claims] 1. A bundle of multiple quartz glass optical fibers is drawn to form multiple fibers with an outer diameter of 1 to 5 mm, and the drawn multiple fibers are coated with paint to a thickness of 100 μm or more. , elongation 3%
The above is a continuous method for producing optical quartz glass-based multiple fibers, which is characterized by forming an adhesive organic polymer layer with a tensile modulus of 1000 Kg/cm 2 or more. 2. The continuous manufacturing method according to claim 1, characterized in that the adhesive organic polymer layer is formed immediately after drawing the multiple fibers and by applying a paint once.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19801881A JPS5899136A (en) | 1981-12-08 | 1981-12-08 | Continuous manufacture of multiple fiber of quartz glass for optical use |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19801881A JPS5899136A (en) | 1981-12-08 | 1981-12-08 | Continuous manufacture of multiple fiber of quartz glass for optical use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5899136A JPS5899136A (en) | 1983-06-13 |
| JPH0224771B2 true JPH0224771B2 (en) | 1990-05-30 |
Family
ID=16384142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19801881A Granted JPS5899136A (en) | 1981-12-08 | 1981-12-08 | Continuous manufacture of multiple fiber of quartz glass for optical use |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5899136A (en) |
-
1981
- 1981-12-08 JP JP19801881A patent/JPS5899136A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5899136A (en) | 1983-06-13 |
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