JPH0357058B2 - - Google Patents

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Publication number
JPH0357058B2
JPH0357058B2 JP57017442A JP1744282A JPH0357058B2 JP H0357058 B2 JPH0357058 B2 JP H0357058B2 JP 57017442 A JP57017442 A JP 57017442A JP 1744282 A JP1744282 A JP 1744282A JP H0357058 B2 JPH0357058 B2 JP H0357058B2
Authority
JP
Japan
Prior art keywords
starting material
base material
optical fiber
burner
refractive index
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
Application number
JP57017442A
Other languages
Japanese (ja)
Other versions
JPS58135147A (en
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to JP57017442A priority Critical patent/JPS58135147A/en
Publication of JPS58135147A publication Critical patent/JPS58135147A/en
Publication of JPH0357058B2 publication Critical patent/JPH0357058B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B37/00Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
    • C03B37/01Manufacture of glass fibres or filaments
    • C03B37/012Manufacture of preforms for drawing fibres or filaments
    • C03B37/014Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD]
    • C03B37/01486Means for supporting, rotating or translating the preforms being formed, e.g. lathes
    • C03B37/01493Deposition substrates, e.g. targets, mandrels, start rods or tubes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P40/00Technologies relating to the processing of minerals
    • Y02P40/50Glass production, e.g. reusing waste heat during processing or shaping
    • Y02P40/57Improving the yield, e-g- reduction of reject rates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Manufacture, Treatment Of Glass Fibers (AREA)

Description

【発明の詳細な説明】 本発明は光フアイバ母材の製造方法に関するも
のであり、単一モードおよび多モード光フアイバ
などすべての光フアイバを作ることができる。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing optical fiber preforms, which can produce all types of optical fibers, including single mode and multimode optical fibers.

従来の光フアイバ母材の製造方法を第1図に示
す。これは火炎加水分解バーナ1でガラス微粒子
を含んだ火炎5を発生させ。これを矢印8方向に
回転しながら矢印7方向へ移動する出発材4に吹
付けてロツド状の多孔質ガラス母材2を成長させ
る。その後加熱源3で焼結して透明な光フアイバ
母材14にする方法である。この方法は、長尺、
大口径、かつ広帯域で低損失の光フアイバが容易
に得られるという特徴を有しているが、本発明者
はこの装置構成で出発材の形状を種々変えて実験
を行つた結果、次のような問題点があることがわ
かつた。
A conventional method for manufacturing an optical fiber base material is shown in FIG. This involves a flame hydrolysis burner 1 generating a flame 5 containing fine glass particles. This is sprayed onto the starting material 4 moving in the direction of arrow 7 while rotating in the direction of arrow 8 to grow a rod-shaped porous glass base material 2. This method is followed by sintering with a heat source 3 to form a transparent optical fiber base material 14. This method uses long
It has the characteristics of being able to easily obtain a large diameter, broadband, and low loss optical fiber, but the inventor of the present invention conducted experiments using this device configuration with various starting material shapes, and found the following results. It turns out that there are some problems.

(1) 出発材の形状として、第2図a〜dについて
検討した。aはムクのガラス棒を用いた単純な
場合であるが、この場合には第3図に示すよう
に、バーナ1からでた火炎5の流れが出発材の
近傍で矢印21に示すような逆流を生ずる。こ
のような逆流を生ずると第3図bに示すように
径方向のガラス微粒子の成長速度が大きくな
り、第3図cのように堆積した多孔質母材の肩
の部分にAに示すようなくびれが生ずる。この
ようなくびれ部分のかさ密度は低いために機械
的シヨツクとかちよつとした温度変化に対して
歪が発生して第3図dのように多孔質母材2が
落下し易く、多孔質母材の作成が不安定であつ
た。また、出発材の底面形状が作成された多孔
質母材の底面形状と相違しているために多孔質
母材を定常状態に保つのに時間がかかるのと、
その再現性に問題があつた。
(1) Figures 2 a to d were examined as the shapes of the starting materials. A shows a simple case using a solid glass rod, but in this case, as shown in Fig. 3, the flow of flame 5 from burner 1 is reversed as shown by arrow 21 near the starting material. will occur. When such a backflow occurs, the growth rate of glass fine particles in the radial direction increases as shown in Figure 3b, and as shown in Figure 3c, the shoulder part of the deposited porous base material has a shape like that shown in A. A constriction occurs. Since the bulk density of such a constricted part is low, distortion occurs due to mechanical shock or sharp temperature changes, and the porous base material 2 tends to fall as shown in Figure 3d. was unstable. In addition, since the bottom surface shape of the starting material is different from the bottom surface shape of the porous base material created, it takes time to maintain the porous base material in a steady state.
There was a problem with its reproducibility.

(2) 第2図bおよびcは上記(1)の問題点を解決さ
せるために、あらかじめ出発材の底面形状を大
きくしておいたものであり、(1)のような問題点
はほぼ解決できるが、多孔質母材を焼結し終つ
た後、出発材と光フアイバ母材の接触面でクラ
ツクが発生し、光フアイバ母材中にもクラツク
が伝わつていくという問題点が生じた。このク
ラツクの発生は、出発材に石英系ガラスを用
い、光フアイバ母材にSiO2−GeO2−P2O5系の
ガラス(SiO2よりも屈折率差が1%以上も高
いガラス)を堆積させているために両者のガラ
スの熱膨張係数のちがいと両者のガラスの接触
面積が大きすぎるためによるものである。
(2) In Figure 2 b and c, the bottom shape of the starting material is made larger in advance in order to solve the problem in (1) above, and the problem in (1) is almost solved. However, after the porous base material is sintered, cracks occur at the contact surface between the starting material and the optical fiber base material, and the cracks propagate into the optical fiber base material. This crack can be caused by using silica-based glass as the starting material and using SiO 2 -GeO 2 -P 2 O 5 -based glass (glass with a refractive index difference of 1% or more higher than that of SiO 2 ) as the optical fiber base material. This is due to the difference in thermal expansion coefficients between the two glasses because they are deposited, and the contact area between the two glasses is too large.

(3) 第2図dは石英ガラス管4′の先端に石英ガ
ラス棒4″(この表面はサンドペーパーなどに
より、粗面に仕上げられ、上記(2)のクラツク発
生を防ぐようにしてある。)をノツクピン22
で固定したものである。この方法では出発材
4′は毎回同じものを使え、4″のみを交換する
ことによつてクラツクの少ない光フアイバ母材
を得ることが可能であるが、4′と4″の中心軸
を一致させることが困難なため、光フアイバ母
材の再現性が悪い。
(3) Figure 2d shows a quartz glass rod 4'' (the surface of which has been roughened with sandpaper or the like to prevent the occurrence of cracks as described in (2) above) at the tip of the quartz glass tube 4'. ) with the knock pin 22
It is fixed at In this method, the same starting material 4' can be used each time, and by replacing only 4'', it is possible to obtain an optical fiber base material with fewer cracks, but it is necessary to align the center axes of 4' and 4''. The reproducibility of the optical fiber base material is poor because it is difficult to do so.

以上のように、従来の技術では高品質光フアイ
バ母材を再現性良く作ることがむずかしく、ま
た、クラツクの発生による多孔質母材の落下、光
フアイバ母材の損失などが生じ、生産性が悪い。
As described above, with conventional techniques, it is difficult to produce high-quality optical fiber preforms with good reproducibility, and cracks may occur, causing the porous preform to fall and optical fiber preforms to be lost, resulting in reduced productivity. bad.

本発明の目的は、前記従来の問題点を解決する
方法を提供することにある。すなわち、多孔質母
材の落下防止、光フアイバ母材のクラツク発生の
防止、高品質光フアイバ母材の製造歩留りの向上
を実現できる光フアイバ母材の製造法を提供する
ことにある。
An object of the present invention is to provide a method for solving the above-mentioned conventional problems. That is, the object of the present invention is to provide a method for manufacturing an optical fiber preform that can prevent the porous preform from falling, prevent the occurrence of cracks in the optical fiber preform, and improve the manufacturing yield of high-quality optical fiber preforms.

本発明は、出発材の先端底面(多孔質母材を成
長させていく側。)形状をl∝r〓sとなるように加
工した石英ガラス棒、あるいは石英ガラス管さら
には屈折率分布をもつた石英系のガラス棒あるい
はガラス管を用いることにより従来法の問題点を
解決するようにしたものである。ただし、l:出
発材底面から引き上げ方向への距離、r:出発材
の半径方向の位置、αs:底面形状分布係数。この
ように出発材の先端をテーパ状の円錐形になるよ
うに引き延ばすことによつて、次のような効果が
期待できる。
The present invention is directed to a quartz glass rod or a quartz glass tube, which is processed so that the shape of the tip bottom surface (the side on which the porous base material is grown) of the starting material is l∝r〓s , or even a quartz glass tube that has a refractive index distribution. This method solves the problems of the conventional method by using a quartz-based glass rod or glass tube. However, l: distance from the bottom of the starting material in the pulling direction, r: position in the radial direction of the starting material, α s : bottom surface shape distribution coefficient. By stretching the tip of the starting material into a tapered conical shape in this way, the following effects can be expected.

(1) 出発材の先端を中心軸上に引き延ばすことに
より、出発材の中心軸が明確になり、バーナと
出発材の中心軸設定などの初期条件の設定が容
易である。
(1) By stretching the tip of the starting material onto the central axis, the central axis of the starting material becomes clear, making it easy to set initial conditions such as setting the central axes of the burner and the starting material.

(2) (1)のように設定すると、バーナからの火炎5
の流れが出発材の外周に沿つて一様に流れるよ
うになり、出発材の底面近傍に第3図に示した
ような逆流が生じなくなる。その結果、多孔質
母材への不均一なストレスが生じなくなり、ク
ラツクの発生による多孔質母材の割れも生じな
い。
(2) When set as in (1), the flame from the burner is 5
The flow uniformly flows along the outer periphery of the starting material, and a backflow as shown in FIG. 3 does not occur near the bottom of the starting material. As a result, uneven stress is not applied to the porous base material, and cracks do not occur in the porous base material.

(3) 出発材のαsを、作成する多孔質母材の底面形
状分布係数(これをαs′と定義する。)の値近傍
にあらかじめ設定しておくと、多孔質母材の作
成過程中に余分な制御(たとえばバーナと出発
材底面間の距離、出発材の引き上げ速度、など
の制御)を必要とせず、容易に所望のαs′をも
つた多孔質母材を作成できる。
(3) If α s of the starting material is set in advance near the value of the bottom shape distribution coefficient (this is defined as α s ′) of the porous base material to be created, the process of creating the porous base material can be A porous base material having a desired α s ' can be easily produced without requiring any extra control (for example, controlling the distance between the burner and the bottom surface of the starting material, the pulling speed of the starting material, etc.).

(3) 出発材の先端がテーパ状の円錐形に引き延ば
されていると、この付近に堆積されたガラス微
粒子が焼結により収縮するときの収縮(圧縮)
応力は第4図aに示すように、径方向および軸
方向に対してほぼ一様の応力が働くのに対し
て、従来の出発材の底面面積が大きい場合に
は、第4図bに示すように、径方向、軸方向で
の応力分布の変化が大きく不均一分布を生ずる
ために、出発材と光フアイバ母材の接触部に歪
が発生(上記歪と両ガラスの熱膨張係数のちが
いによる歪)して光フアイバ母材にクラツクが
入る。極端な場合には光フアイバ母材の半分以
上にクラツクが入り、光フアイバ母材として使
用不能になる。本発明の場合にはほとんどクラ
ツクが発生しない。
(3) When the tip of the starting material is stretched into a tapered conical shape, the glass particles deposited near this point shrink (compress) when they shrink due to sintering.
As shown in Figure 4a, the stress is almost uniform in the radial and axial directions, whereas when the bottom surface area of the conventional starting material is large, the stress is as shown in Figure 4b. As shown in the figure, the stress distribution changes greatly in the radial and axial directions, resulting in a non-uniform distribution, which causes strain at the contact area between the starting material and the optical fiber base material (due to the above strain and the difference in the thermal expansion coefficients of the two glasses). cracks in the optical fiber base material. In extreme cases, cracks occur in more than half of the optical fiber base material, making it unusable as an optical fiber base material. In the case of the present invention, almost no cracks occur.

(4) 出発材に、光フアイバと同じような屈折率分
布をもせることにより、出発材のもう一方の先
端からレーザビームを入射させ、底面の先鋭部
から出射させるようにしておけば、出発材の中
心軸とバーナの中心軸との相対位置を容易に設
定することができ、また、多孔質母材の焼結時
における透明化プロセスの監視にも利用でき
る。さらに、出発材の中心部をSiO2または、
屈折率を高める、ドーパント(Ge,Pなど)
を含んだSiO2とし、外周部を屈折率を低める
ドーパント(B,Fなど)を含んだSiO2また
はSiO2を用いれば、光フアイバ母材との熱膨
張係数を接近させることができるので、この熱
膨張係数の差による歪の発生を防ぐことができ
る。
(4) By giving the starting material a refractive index distribution similar to that of an optical fiber, the laser beam can be incident on the other end of the starting material and emitted from the sharp end of the bottom surface. The relative position between the central axis of the material and the central axis of the burner can be easily set, and it can also be used to monitor the transparency process during sintering of a porous base material. Furthermore, the center of the starting material is SiO 2 or
Dopants (Ge, P, etc.) that increase the refractive index
By using SiO 2 or SiO 2 containing a dopant (B, F, etc.) that lowers the refractive index in the outer periphery, the coefficient of thermal expansion can be made close to that of the optical fiber base material. It is possible to prevent distortion from occurring due to this difference in thermal expansion coefficients.

第5図a,bは本発明の出発材の断面図、正面
図を示したものであり、cは出発材の軸方向長さ
lとそのlにおける径方向位置rとの関係を示し
たグラフである。出発材の材質は市販の石英ガラ
ス棒(外径数mmから数10mm、好ましい値は10数
mm、長さ1m)であり、その先端部をバーナで加
熱して引き延ばし加工した。低面のαsは0.3から
3.5の範囲が好ましい。これは、第3図に示した
ような逆流防止の上から好ましい。このαsの決定
は、出発材の底面部をテレビカメラで観測し、所
望のαsの画面と比較しながら行つた。なお、先端
部と位置0は出発材の中心軸と一致させるのが好
ましく、また位置0に対してr方向には同心状で
あることが好ましい。
Figures 5a and 5b show a cross-sectional view and a front view of the starting material of the present invention, and c is a graph showing the relationship between the axial length l of the starting material and the radial position r at that l. It is. The starting material is a commercially available quartz glass rod (outer diameter of several mm to several tens of mm, preferably 10 mm).
mm, length 1 m), and its tip was heated with a burner and stretched. α s of the lower surface is from 0.3
A range of 3.5 is preferred. This is preferable from the standpoint of preventing backflow as shown in FIG. This α s was determined by observing the bottom surface of the starting material with a television camera and comparing it with the desired α s screen. Note that the tip and position 0 are preferably aligned with the central axis of the starting material, and are preferably concentric with position 0 in the r direction.

第6図は出発材にガラス管を用い、その先端部
を引き延ばしたものである。実施例では石英ガラ
ス(外径12mm、内径約10mm、長さ1m)を用いた
が、石英ガラス棒に比し真直度が良好であるの
で、出発材としてはより好都合であつた。最先端
の0点は完全に密封されていなくてもよく、たと
えば1mm程度の穴があいていてもさしつかえなか
つた。また、ガラス管内へ一方からレーザビーム
を通して管の中心軸とバーナの中心軸との相対位
置関係を設定するのも容易であつた。ガラス管の
直径は数mmから数10mmのものを使用できる。底面
部のαsは前記と同様の値が適用できる。
In FIG. 6, a glass tube is used as the starting material, and the tip thereof is stretched. In the examples, quartz glass (outer diameter 12 mm, inner diameter approximately 10 mm, length 1 m) was used, but since it has better straightness than a quartz glass rod, it was more convenient as a starting material. The leading edge 0 point did not have to be completely sealed; for example, a hole of about 1 mm could be present. It was also easy to set the relative positional relationship between the central axis of the tube and the central axis of the burner by passing a laser beam into the glass tube from one side. The diameter of the glass tube can range from several mm to several tens of mm. The same value as above can be applied to α s of the bottom surface portion.

第7図は出発材としてガラス棒を用いた場合の
径方向断面図の屈折率分布を示したもので、aの
ように石英ガラス棒の場合の他に、bのステツプ
型屈折率分布、c,dの集束型屈折率分布のもの
も使える。屈折率差Δnは0.数%から数%の範囲
内から選べ、光フアイバ母材の屈折率分布に応じ
て選ぶならばより有効であることは前記説明から
明らかである。b〜dの屈折率分布を有する出発
材を作る方法として、石英ガラス棒の外周に外付
けCVD法(火炎加水分解バーナでガラス微粒子
を吹付ける方法)でB2O3を含むSiO2ガラスを堆
積、焼結して得るか、ほう酸水溶液に石英ガラス
棒を浸した後、熱処理によつて得るか、あるい
は、有機シラン系のアルコール溶液(たとえば商
品名シリカフイルム。)を石英ガラス棒に塗布、
焼結して得る、などの通常よく知られた方法を適
用することができる。
Figure 7 shows the refractive index distribution in a radial cross-sectional view when a glass rod is used as the starting material. , d can also be used. It is clear from the above description that the refractive index difference Δn can be selected from within the range of several 0.0% to several percent, and that it is more effective if it is selected according to the refractive index distribution of the optical fiber base material. As a method for producing a starting material with a refractive index distribution of b to d, SiO 2 glass containing B 2 O 3 was attached to the outer periphery of a quartz glass rod using an external CVD method (a method of spraying glass particles with a flame hydrolysis burner). It can be obtained by depositing and sintering, or by immersing a quartz glass rod in an aqueous solution of boric acid and then heat-treating it, or by applying an organic silane-based alcohol solution (for example, the product name is Silica Film) to a quartz glass rod.
Generally well-known methods such as obtaining by sintering can be applied.

第8図は出発材としてガラス管を用いた場合の
径方向断面図内の屈折率分布を示したものであ
る。aは石英ガラス管の場合、a〜dはガラス管
の内面に屈折率を高めるドーパントを堆積させた
場合、である。石英ガラス管の外側に屈折率を低
めるドーパント(B,Fなど)を堆積させた石英
ガラス管を用いてもよい。ガラス管の内面にガラ
ス棒膜を堆積させる方法はよく知られた内付け
CVD法を用いればよい。なお、第7図のガラス
棒と第8図のガラス管を用い、ロツドインチユー
ブ法で種々を屈折率分布をもつた出発材も作るこ
とができ、この場合も本発明の出発材の一つとし
て構成される。
FIG. 8 shows the refractive index distribution in a radial cross-sectional view when a glass tube is used as the starting material. a is the case of a quartz glass tube, and a to d are the cases where a dopant that increases the refractive index is deposited on the inner surface of the glass tube. A quartz glass tube in which a dopant (B, F, etc.) that lowers the refractive index is deposited on the outside of the quartz glass tube may be used. The method of depositing a glass rod film on the inner surface of a glass tube is a well-known internal attachment method.
CVD method may be used. In addition, starting materials with various refractive index distributions can be made by the rod incubation method using the glass rod shown in FIG. 7 and the glass tube shown in FIG. 8, and in this case, one of the starting materials of the present invention constituted as one.

次に、第1図の光フアイバ母材製造装置に本発
明の出発材を用いた場合の光フアイバ母材の特性
について述べる。出発材として、第5図に示すよ
うな石英ガラス棒(外径12mm、長さ1m)を用
い、先端部のαsを2.0〜2.5として光フアイバ母材
を28本試作した。ただし、出発材は同一のものを
使用し、光フアイバ母材を焼結後、出発材と光フ
アイバ母材の接触部をバーナで焼き切り、再度先
端部を所望のαsとなるように加工して使用する方
法を用いた。まず多孔質母材の作成条件を示す。
外径17.8mmの同心状の4重管バーナ1の中心管1
01にSiCl4(0.5/min)、GeCl4(0.18/min)、
POCl3(0.1/min)をArをキヤリヤガスとして
送り込み、その外側の管102にAr(0.9/
min)を、その次の管103内にH2(3/
min)、最外管104内にO2(6/min)をそれ
ぞれ流した。そしてバーナの外周に同心状の3重
管からなる保護管を用い(図中に記載せず)、そ
れぞれの保護管内にN2ガスを10/min流した。
反応容器6内の圧力を−0.1mmAqになるように差
圧計15出力を制御回路16を通して排気速度調
整装置17にフイードバツクした。このような条
件下で、出発材とバーナの中心軸を一致させて多
孔質母材(外径約70mm、長さ300mm)を作成した。
この多孔質母材を焼結は1650℃(ヒータの表面温
度を光高温計で測定した値)のHeとCl2の雰囲気
で行つた。その結果、多孔質母材のクラツク発生
による落下は一度もたなかつた。また光フアイバ
母材と出発材との接触面での割れも一度も生じな
かつた。多孔質母材のαs′の変動も±10%以下で
あつた。またこの光フアイバ母材を石英ガラス管
内に入れ、ロツドインチユーブ化した後、光フア
イバ(外径150μm、コア径80μm、屈折率差約1
%)とした結果、波長0.85μmで損失は3dB/Km
以下、帯域600MHz・Km以上の高品質特性を有す
る光フアイバを得ることができた。
Next, the characteristics of the optical fiber preform when the starting material of the present invention is used in the optical fiber preform manufacturing apparatus shown in FIG. 1 will be described. Using a quartz glass rod (outer diameter 12 mm, length 1 m) as shown in FIG. 5 as a starting material, 28 optical fiber base materials were prepared by setting α s of the tip portion to 2.0 to 2.5. However, the same starting material is used, and after sintering the optical fiber base material, the contact area between the starting material and the optical fiber base material is burnt off with a burner, and the tip is processed again to the desired α s . The method used was used. First, we will show the conditions for creating the porous base material.
Center tube 1 of concentric quadruple tube burner 1 with an outer diameter of 17.8 mm
01 SiCl 4 (0.5/min), GeCl 4 (0.18/min),
POCl 3 (0.1/min) is fed with Ar as a carrier gas, and Ar (0.9/min) is fed into the outer pipe 102.
min) into the next tube 103 .
min), and O 2 (6/min) was flowed into the outermost tube 104, respectively. A protective tube consisting of concentric triple tubes was used around the burner (not shown in the figure), and N 2 gas was flowed at 10/min into each protective tube.
The output of the differential pressure gauge 15 was fed back to the pumping speed regulator 17 through the control circuit 16 so that the pressure inside the reaction vessel 6 was -0.1 mmAq. Under these conditions, a porous base material (outer diameter approximately 70 mm, length 300 mm) was created by aligning the central axes of the starting material and the burner.
This porous base material was sintered in an atmosphere of He and Cl 2 at 1650°C (the value measured by the surface temperature of the heater with an optical pyrometer). As a result, the porous base material never fell due to cracks. Furthermore, no cracking occurred at the contact surface between the optical fiber base material and the starting material. The variation in α s ′ of the porous base material was also less than ±10%. In addition, this optical fiber base material was put into a quartz glass tube and made into a rod inch tube.
%), the loss is 3dB/Km at a wavelength of 0.85μm.
Below, we were able to obtain an optical fiber with high quality characteristics with a bandwidth of 600MHz/Km or more.

本発明は上記実施例に限定されない。出発材の
長さは数10cmから数mのものでもよい。出発材の
材質はSiO2を主成分とするものであればよく、
バイコールガラス(商品名、コーニングガラス
製)でもよい。光フアイバ母材の製造法は第1図
の方法に限定されず、従来用いられている出発材
を用いた気相軸付寸法のすべてに適用できる。
The invention is not limited to the above embodiments. The length of the starting material may be from several tens of centimeters to several meters. The material of the starting material may be one containing SiO 2 as the main component.
Vycor glass (trade name, manufactured by Corning Glass) may also be used. The method for manufacturing the optical fiber base material is not limited to the method shown in FIG. 1, but can be applied to all gas phase shaft dimensions using conventionally used starting materials.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は従来の光フアイバ母材製造法の概略
図、第2図は従来、本発明者が用いてきた出発材
の形状(断面図)概略図、第3図は従来の出発材
を用いた場合の多孔質母材の成長過程を説明する
図、第4図は多孔質母材の焼結時に発生する収縮
応力の定性的説明図で、aは本発明の場合、bは
従来の場合、第5,6図は本発明の出発材の概略
図、第7,8図は出発材の屈折率分布を示したも
のである。 6……反応容器、9,10……ガス導入管、1
1,12……ガスの流れ方向、13……引上げ装
置、18……出発材取付けチヤツク、19……バ
ーナ取付け支持部、20……バーナ微動装置。
Fig. 1 is a schematic diagram of a conventional optical fiber base material manufacturing method, Fig. 2 is a schematic diagram of the shape (cross-sectional view) of the starting material that the present inventor has conventionally used, and Fig. 3 is a schematic diagram of the conventional method for producing an optical fiber base material. Figure 4 is a qualitative illustration of the shrinkage stress generated during sintering of the porous base material, where a is the case of the present invention and b is the conventional case. , FIGS. 5 and 6 are schematic diagrams of the starting material of the present invention, and FIGS. 7 and 8 show the refractive index distribution of the starting material. 6... Reaction container, 9, 10... Gas introduction pipe, 1
DESCRIPTION OF SYMBOLS 1, 12... Gas flow direction, 13... Pulling device, 18... Starting material mounting chuck, 19... Burner mounting support part, 20... Burner fine movement device.

Claims (1)

【特許請求の範囲】[Claims] 1 排気装置付反応容器内の下部にバーナを、上
部に回転しつつ移動する出発材を配置し、バーナ
から発生させたガラス微粒子を出発材に吹付けて
多孔質母材を軸方向に成長させ、この母材を出発
材と同軸上に置かれた加熱炉に挿入してゆくこと
により光フアイバ母材を製造する方法において、
前記出発材に、径方向断面内で光フアイバと同様
の屈折率分布をもつた石英系ガラス棒および径方
向断面内で屈折率分布をもつた石英系ガラス管の
うちの一つを用い、多孔質母材を成長させていく
方の出発材の先端をテーパ状の円錐形になるよう
に引き延ばした出発材を用いたことを特徴とする
光フアイバ母材の製造方法。
1 A burner is placed at the bottom of a reaction vessel equipped with an exhaust system, and a rotating and moving starting material is placed at the top, and glass fine particles generated from the burner are sprayed onto the starting material to grow the porous base material in the axial direction. , a method for manufacturing an optical fiber base material by inserting this base material into a heating furnace placed coaxially with the starting material,
As the starting material, one of a quartz glass rod having a refractive index distribution similar to that of an optical fiber in the radial cross section and a quartz glass tube having a refractive index distribution in the radial cross section is used. 1. A method for producing an optical fiber preform, characterized in that a starting material on which the fiber preform is grown is elongated so that the tip of the starting material is elongated into a tapered conical shape.
JP57017442A 1982-02-08 1982-02-08 Preparation of base material for optical fiber Granted JPS58135147A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57017442A JPS58135147A (en) 1982-02-08 1982-02-08 Preparation of base material for optical fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57017442A JPS58135147A (en) 1982-02-08 1982-02-08 Preparation of base material for optical fiber

Publications (2)

Publication Number Publication Date
JPS58135147A JPS58135147A (en) 1983-08-11
JPH0357058B2 true JPH0357058B2 (en) 1991-08-30

Family

ID=11944137

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57017442A Granted JPS58135147A (en) 1982-02-08 1982-02-08 Preparation of base material for optical fiber

Country Status (1)

Country Link
JP (1) JPS58135147A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60260432A (en) * 1984-06-04 1985-12-23 Sumitomo Electric Ind Ltd Manufacture of preform for optical fiber
JPS6197140A (en) * 1984-10-18 1986-05-15 Asahi Glass Co Ltd Improved seed rod for preparing parent material for porous quartz glass
JPS61222931A (en) * 1985-03-27 1986-10-03 Furukawa Electric Co Ltd:The Deposition of fine glass particle
JP6916622B2 (en) * 2017-01-27 2021-08-11 信越石英株式会社 Manufacturing method of porous quartz glass base material

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5717439A (en) * 1980-07-04 1982-01-29 Hitachi Ltd Manufacture of base material for optical fiber
JPS57135737A (en) * 1981-02-13 1982-08-21 Showa Electric Wire & Cable Co Ltd Starting material for manufacturing of optical fiber by v.a.d. process

Also Published As

Publication number Publication date
JPS58135147A (en) 1983-08-11

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