JPS63139025A - Production of optical fiber base material - Google Patents
Production of optical fiber base materialInfo
- Publication number
- JPS63139025A JPS63139025A JP28507986A JP28507986A JPS63139025A JP S63139025 A JPS63139025 A JP S63139025A JP 28507986 A JP28507986 A JP 28507986A JP 28507986 A JP28507986 A JP 28507986A JP S63139025 A JPS63139025 A JP S63139025A
- Authority
- JP
- Japan
- Prior art keywords
- diameter
- base material
- optical fiber
- cladding
- core diameter
- 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
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
- C03C25/66—Chemical treatment, e.g. leaching, acid or alkali treatment
- C03C25/68—Chemical treatment, e.g. leaching, acid or alkali treatment by etching
-
- 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
- C03C15/00—Surface treatment of glass, not in the form of fibres or filaments, by etching
Landscapes
- Chemical & Material Sciences (AREA)
- 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)
- General Life Sciences & Earth Sciences (AREA)
- Glass Melting And Manufacturing (AREA)
- Manufacture, Treatment Of Glass Fibers (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、光ファイバ母材の製造方法に関し、特に石英
ジャケット管を用いず、光ファイバ母材のすべてをガラ
ス微粒子集合体で生成させた後、焼結し、脱泡して光フ
ァイバ母材を製造する方法(以下、全合成法という)に
際して、過剰のクラッド部をエツチングすることにより
、コア径とクラッド径の比を適切にする製造方法に関す
る。[Detailed Description of the Invention] (Industrial Application Field) The present invention relates to a method for manufacturing an optical fiber preform, and in particular, the present invention relates to a method for manufacturing an optical fiber preform, in which the optical fiber preform is entirely made of an aggregate of glass particles without using a quartz jacket tube. In the method of manufacturing an optical fiber preform by sintering and defoaming (hereinafter referred to as the total synthesis method), the excess cladding is etched to ensure an appropriate ratio of the core diameter to the cladding diameter. Regarding the method.
(従来技術)
従来・光ファイバ母材は、ガラス微粒子合成トーチを用
いて、高純度のガラス形成原料ガスを高温で加熱し、加
水分解反応を起させて酸化物のガラス微粒子を合成し、
それを回転させて引あげられる出発部材の先端に堆積さ
せ、成長させて作った軸付は法によるガラス微粒子集合
体を、高温の炉で焼結し、脱泡させてコア部又はコア部
とクラッド部の一部を形成する透明なガラス母材を得た
後、この透明ガラス母材を適当な径まで引き伸して、ク
ラッドまたはクラッドの一部とする石英ジャケット管中
に挿入して加熱し、ジャケット管と透明ガラスとを溶着
させることによって光ファイバ用ガラス母材を製造して
いた。(Prior art) Conventional optical fiber base material is produced by heating high-purity glass forming raw material gas at high temperature using a glass particle synthesis torch to cause a hydrolysis reaction to synthesize oxide glass particles.
The glass particles are deposited and grown on the tip of the starting member that is rotated and pulled up, and the glass particle aggregate is then sintered in a high-temperature furnace and degassed to form the core part or core part. After obtaining a transparent glass base material that will form part of the cladding part, this transparent glass base material is stretched to an appropriate diameter, inserted into the cladding or a quartz jacketed tube that will become part of the cladding, and heated. However, a glass preform for optical fibers was manufactured by welding a jacket tube and transparent glass.
この方法においては、透明ガラス母材の引き伸し径を調
整することによって、適切なコア径とクラッド径の比を
もった光ファイバ母材を得ることができる。しかし、こ
の方法では、高価な石英ジャケット管を使用するため、
光ファイバ母材の製造コストが大きいという問題があり
、更に、ジャケット管中に含有するOHiがコア部に拡
散し、ファイバの光損失を高くするといった問題があっ
た。In this method, by adjusting the drawn diameter of the transparent glass preform, it is possible to obtain an optical fiber preform having an appropriate ratio of core diameter to cladding diameter. However, this method uses expensive quartz jacketed tubes, so
There is a problem that the manufacturing cost of the optical fiber preform is high, and there is also a problem that OHi contained in the jacket tube diffuses into the core portion, increasing optical loss of the fiber.
そのため、石英ジャケット管を用いないで、すべてガラ
ス微粒子から光ファイバ母材を製造するという全合成法
が用いられている。Therefore, a total synthesis method is used in which the optical fiber preform is manufactured entirely from glass particles without using a quartz jacket tube.
全合成法のうちの一つは、コア部とクラッド部を形成す
る透明ガラス母材をそのまま光ファイバ母材とするもの
で、コア径に対するクラッド径の比が適切な値になるよ
うに、ガラス微粒子集合体を生成させる方法である。す
なわち、ガラス微粒子集合体の作製および畜温炉による
焼結、脱泡処理をそれぞれ1回の工程だけ行って完成品
の光ファイバ母材とする方法である。One of the total synthesis methods uses the transparent glass base material that forms the core and cladding parts as the optical fiber base material. This is a method of generating fine particle aggregates. That is, this is a method in which the preparation of a glass particle aggregate, the sintering in an oven, and the degassing treatment are each carried out only once to obtain a finished optical fiber preform.
他の全合成法としては、透明ガラス母材の上に、ガラス
微粒子を更に付着せしめ、それを高温の炉で焼結し、脱
泡させることにより、コア径に対するクラッド径の比を
適切にし、完成品の光ファイバ母材とする方法である。Another total synthesis method involves further adhering glass particles onto a transparent glass base material, sintering them in a high-temperature furnace, and degassing them to achieve an appropriate ratio of the cladding diameter to the core diameter. This method is used as a finished optical fiber base material.
これらの全合成法は、高価な石英ジャケット管を用いな
いという利点があるものの、コア径に対するクラッド径
の比を適切にするための調整を、すべてガラス微粒子の
堆積の厚さで行わなければならない問題があり、しかも
、その後の焼結、脱泡処理によってガラス微粒子の集合
体は、大幅な収縮を起すため、この方法でコア径に対す
るクラッド径の比を適切にすることは、極めて困難であ
り、且つ歩留りが低いという問題がある。Although these total synthesis methods have the advantage of not using expensive quartz jacketed tubes, adjustments must be made to the thickness of the glass particle deposition to obtain an appropriate ratio of cladding diameter to core diameter. Furthermore, it is extremely difficult to obtain an appropriate ratio of the cladding diameter to the core diameter using this method, as the aggregate of glass particles undergoes significant shrinkage during the subsequent sintering and defoaming treatments. , and the yield is low.
(発明が解決しようとする問題点)
本発明は、上記の全合成法による問題点、すなわち、適
切なコア径とクラッド径の比を存する光ファイバ母材が
再現よく製造できないという問題を解決し、容易に安価
な光ファイバ母材を製造する方法を提供することを目的
とするものである。(Problems to be Solved by the Invention) The present invention solves the problem caused by the above-mentioned total synthesis method, that is, it is impossible to reproducibly produce an optical fiber preform having an appropriate ratio of core diameter to cladding diameter. The object of the present invention is to provide a method for manufacturing an optical fiber preform easily and inexpensively.
(問題点を解決するための手段)
本発明者らは、上記の問題を解決するために鋭意検討を
重ねた結果、本発明を完成させたものである。(Means for Solving the Problems) The present inventors have completed the present invention as a result of intensive studies to solve the above problems.
本発明は、ガラス微粒子集合体を高温で焼結し、脱泡処
理して光ファイバ母材を製造する方法において、予めコ
ア径に対するクラッド径の比が適切値よりも大きくなる
ようにクラッド部を形成させて透明ガラス母材を作製し
たのち、エツチング液を用いてコア径に対するクラッド
径の比が適切な値になるまで、過剰のクラッド部のガラ
ス体をエツチングし、減少させることを特徴とする光フ
ァイバ母材の製造方法である。The present invention provides a method for manufacturing an optical fiber preform by sintering a glass particle aggregate at high temperature and degassing it, in which the cladding portion is preliminarily adjusted so that the ratio of the cladding diameter to the core diameter is larger than an appropriate value. After forming a transparent glass base material, the excess glass in the cladding portion is etched and reduced using an etching solution until the ratio of the cladding diameter to the core diameter becomes an appropriate value. This is a method for manufacturing an optical fiber preform.
以下、本発明の製造方法の構成について、更に説明する
。The configuration of the manufacturing method of the present invention will be further explained below.
ガラス微粒子集合体を高温で焼結し、脱泡処理して光フ
ァイバ母材を製造する方法において、予めコア径に対す
るクラッド径の比が適切値よりも太き(なるようにクラ
ッド部を形成させて透明ガラス母材を作製するとは、コ
ア径とクラッド径の比が適切値よりも、クラッド径が大
きくなるようにガラス微粒子集合体を作製し、これを高
温の炉で焼結し、脱泡処理して透明なガラス母材を得た
後、この透明ガラス母材の屈折率分布を測定し、コア径
を求めて、適切なりラッド径を知得するか、又は、透明
ガラス母材の外周上に、コア径とクラッド径の比が適切
値よりもクラッド径が大きくなるように、ガラス微粒子
を付着させて、それを再び高温の炉で焼結し、脱泡処理
して透明なガラス母材を得た後、前記と同様に屈折率分
布を測定し、コア径を求めて、適切なりラッド径を知得
するものである。In the method of manufacturing an optical fiber base material by sintering a glass particle aggregate at high temperature and degassing it, the cladding portion is formed in advance so that the ratio of the cladding diameter to the core diameter is thicker than an appropriate value. To create a transparent glass base material, we create a glass particle aggregate so that the cladding diameter is larger than the appropriate ratio of core diameter to cladding diameter, sinter this in a high-temperature furnace, and degas it. After processing to obtain a transparent glass base material, measure the refractive index distribution of this transparent glass base material to determine the core diameter and obtain the appropriate rad diameter, or Then, fine glass particles are attached so that the cladding diameter is larger than the appropriate value for the ratio of core diameter to cladding diameter, and it is sintered again in a high-temperature furnace and degassed to create a transparent glass base material. After obtaining the rad diameter, the refractive index distribution is measured in the same manner as described above, the core diameter is determined, and the appropriate rad diameter is obtained.
本発明で使用するエツチング液とは、フッ化水素酸と硝
酸との混合水溶液であって、15〜20%フッ化水素酸
と15〜20%硝酸との混合水溶液が特に好ましいもの
として使用できる。The etching solution used in the present invention is a mixed aqueous solution of hydrofluoric acid and nitric acid, and a mixed aqueous solution of 15 to 20% hydrofluoric acid and 15 to 20% nitric acid is particularly preferably used.
(作 用)
本発明によれば、予め正確なコア径が測定され、この値
から適切なりラッド径を決定することができるため、適
切なりラッド径になるまで過剰のクラッド部をエツチン
グすることにより、確実にコア径に対する適切なりラッ
ド径の比をもった再現性にすぐれた光ファイバ母材を容
易に効率よく製造することができる作用がある。(Function) According to the present invention, since an accurate core diameter is measured in advance and an appropriate rad diameter can be determined from this value, the excess cladding portion can be etched until an appropriate rad diameter is obtained. This has the effect of making it possible to easily and efficiently manufacture an optical fiber preform with excellent reproducibility and having an appropriate ratio of the rad diameter to the core diameter.
(実施例)
以下、実施例にもとづいて本発明を更に説明するが、本
発明はかかる実施例のみに限定されるものでない。(Examples) Hereinafter, the present invention will be further explained based on Examples, but the present invention is not limited only to these Examples.
実施例1
コア径とクラッド径の比が1:1.25の光ファイバ母
材の製造方法について説明する。Example 1 A method for manufacturing an optical fiber preform having a core diameter to cladding diameter ratio of 1:1.25 will be described.
気相軸付は法によって、コア部とクラッド部の径がそれ
ぞれ約60mmと約80闘のガラス微粒子集合体を作製
した。これを1500℃に加熱した電気炉中で焼結し、
脱泡処理して透明なガラス母材を得た。これを空間フィ
ルタリング法を用いて屈折率分布を測定したところ、コ
ア径は31mm、クラッド径は41mmであった。Glass fine particle aggregates with core and cladding diameters of about 60 mm and about 80 mm, respectively, were prepared by the vapor phase attachment method. This is sintered in an electric furnace heated to 1500°C,
A transparent glass base material was obtained by defoaming treatment. When the refractive index distribution of this was measured using a spatial filtering method, the core diameter was 31 mm and the cladding diameter was 41 mm.
したがって適切なりラッド径は31 Xl、25=38
.75mmであればよいことが判った。そこで、透明ガ
ラス母材をHF15%、HNOz15%のエツチング水
溶液に4日間浸漬したところ、クラッド径が40mmに
減少した。更に同じエツチング水溶液に5日間浸漬した
結果、クラッド径を38.75 mmにすることができ
た。実施例かられかるように、コア径とクラッド径の比
が正確に1:1.25の光ファイバ母材とすることがで
きた。Therefore, the appropriate rad diameter is 31 Xl, 25 = 38
.. It turns out that 75 mm is sufficient. Therefore, when the transparent glass base material was immersed in an etching aqueous solution containing 15% HF and 15% HNOz for 4 days, the cladding diameter was reduced to 40 mm. Further, as a result of immersion in the same etching aqueous solution for 5 days, the cladding diameter could be reduced to 38.75 mm. As can be seen from the examples, it was possible to obtain an optical fiber preform in which the ratio of the core diameter to the cladding diameter was exactly 1:1.25.
実施例2
コア径とクラッド径の比が1:15の光ファイバ母材の
製造方法について説明する。Example 2 A method for manufacturing an optical fiber preform having a core diameter to cladding diameter ratio of 1:15 will be described.
気相軸付は法によって、コア径とクラッド径がそれぞれ
約15mmと約120mmのガラス微粒子集合体を作製
した。これを1500℃に加熱した電気炉中で焼結し、
脱泡処理して透明なガラス母材を得た。このガラス母材
の外径は約58mmであった。これをガラス旋盤で外径
20mmφまで正確に延伸し、更にその外周上にガラス
微粒子を堆積させ、その外径を約94mmとした。Glass fine particle aggregates having core diameters and cladding diameters of about 15 mm and about 120 mm, respectively, were prepared by a vapor phase axial attachment method. This is sintered in an electric furnace heated to 1500°C,
A transparent glass base material was obtained by defoaming treatment. The outer diameter of this glass base material was approximately 58 mm. This was accurately stretched to an outer diameter of 20 mmφ using a glass lathe, and glass fine particles were further deposited on the outer periphery to give an outer diameter of about 94 mm.
これを再び1500℃に加熱した電気炉中で焼結し、脱
泡処理して透明なガラス母材を得た。This was sintered again in an electric furnace heated to 1500°C, and subjected to degassing treatment to obtain a transparent glass base material.
これを空間フィルタリング法を用いて屈折率分布を測定
したところ、コア径2.6 mm、クランド径は39
、6n++nであった。したがって適切なりランド径は
2.6X 15 = 39mmであることが判った。When we measured the refractive index distribution using the spatial filtering method, we found that the core diameter was 2.6 mm and the crund diameter was 39 mm.
, 6n++n. Therefore, it was found that the appropriate land diameter is 2.6 x 15 = 39 mm.
そこで得られた透明ガラス母材をHF15%、HNo、
15%のエツチング水溶液に40時間浸漬した結果、ク
ラッド径を39mmにすることができた。実施例かられ
かるように、コア径とクラッド径の比が正確に1=15
の光ファイバ母材とすることができた。The transparent glass base material obtained therein was mixed with 15% HF, HNo,
As a result of immersion in a 15% etching aqueous solution for 40 hours, the cladding diameter could be set to 39 mm. As can be seen from the example, the ratio of the core diameter to the cladding diameter is exactly 1=15.
could be used as an optical fiber base material.
(発明の効果)
以上、説明した如く、本発明によって製造された光ファ
イバ母材は、クラッド部をエツチングすることにより、
コア径に対するクラッド径の比が正確に調整できるので
、再現性が高(歩留りよく製造できる効果は経済的に寄
与する度合が大である。(Effects of the Invention) As explained above, the optical fiber preform manufactured by the present invention has the following properties by etching the cladding part.
Since the ratio of the cladding diameter to the core diameter can be adjusted accurately, the reproducibility is high (the effect of being able to manufacture with high yields has a large economic contribution).
Claims (1)
ァイバ母材を製造する方法において、予めコア径に対す
るクラッド径の比が適切値よりも大きくなるように、ク
ラッド部を形成させて透明ガラス母材を作製したのち、
エッチング液を用いてコア径に対するクラッド径の比が
適切な値になるまで、過剰のクラッド部のガラス体をエ
ッチングし、減少させることを特徴とする光ファイバ母
材の製造方法。In a method of manufacturing an optical fiber preform by sintering a glass particle aggregate at high temperature and degassing it, the cladding portion is formed in advance so that the ratio of the cladding diameter to the core diameter is larger than an appropriate value. After creating a transparent glass base material,
A method for manufacturing an optical fiber preform, comprising etching and reducing excess glass in the cladding portion using an etching solution until the ratio of the cladding diameter to the core diameter reaches an appropriate value.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28507986A JPS63139025A (en) | 1986-11-29 | 1986-11-29 | Production of optical fiber base material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28507986A JPS63139025A (en) | 1986-11-29 | 1986-11-29 | Production of optical fiber base material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63139025A true JPS63139025A (en) | 1988-06-10 |
JPH0465018B2 JPH0465018B2 (en) | 1992-10-16 |
Family
ID=17686873
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28507986A Granted JPS63139025A (en) | 1986-11-29 | 1986-11-29 | Production of optical fiber base material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63139025A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005187242A (en) * | 2003-12-25 | 2005-07-14 | Namiki Precision Jewel Co Ltd | Etching method for optical fiber |
US8671892B2 (en) | 2009-09-03 | 2014-03-18 | Honda Motor Co., Ltd. | Radiator cooling structure for water-cooled power unit |
-
1986
- 1986-11-29 JP JP28507986A patent/JPS63139025A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005187242A (en) * | 2003-12-25 | 2005-07-14 | Namiki Precision Jewel Co Ltd | Etching method for optical fiber |
US8671892B2 (en) | 2009-09-03 | 2014-03-18 | Honda Motor Co., Ltd. | Radiator cooling structure for water-cooled power unit |
Also Published As
Publication number | Publication date |
---|---|
JPH0465018B2 (en) | 1992-10-16 |
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