JPS6186437A - Manufacturing method of optical fiber base material - Google Patents
Manufacturing method of optical fiber base materialInfo
- Publication number
- JPS6186437A JPS6186437A JP59206935A JP20693584A JPS6186437A JP S6186437 A JPS6186437 A JP S6186437A JP 59206935 A JP59206935 A JP 59206935A JP 20693584 A JP20693584 A JP 20693584A JP S6186437 A JPS6186437 A JP S6186437A
- Authority
- JP
- Japan
- Prior art keywords
- optical fiber
- manufacturing
- chamber
- base material
- internal pressure
- 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 description 25
- 239000000463 material Substances 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 239000011521 glass Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 16
- 239000007789 gas Substances 0.000 claims description 14
- 238000009826 distribution Methods 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- IEXRMSFAVATTJX-UHFFFAOYSA-N tetrachlorogermane Chemical compound Cl[Ge](Cl)(Cl)Cl IEXRMSFAVATTJX-UHFFFAOYSA-N 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 6
- 239000010453 quartz Substances 0.000 description 4
- 230000000737 periodic effect Effects 0.000 description 3
- 239000004071 soot Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000006121 base glass Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
- C03B37/01—Manufacture of glass fibres or filaments
- C03B37/012—Manufacture of preforms for drawing fibres or filaments
- C03B37/014—Manufacture 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]
- C03B37/0144—Means for after-treatment or catching of worked reactant gases
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Glass Melting And Manufacturing (AREA)
- Manufacture, Treatment Of Glass Fibers (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[発明の青電と目的1
本発明は、気相軸付(VAD)法による光フアイバC1
材の製造方法に関するものである。[Detailed Description of the Invention] [Blue electricity and object 1 of the invention]
The invention relates to a method for manufacturing materials.
一般に、VAD法による光ファイバ母Hの製造方法4J
m産性において著しく=Jぐれている。そして、ベー
スガラスとなる塩化珪素(S ! Cf’ 4 )等の
原石ガスと、屈折率を制御するための塩化ゲルマニウム
(GeCj!t)、塩化酸化P’l (P OCで1)
等の原料ガスを酸水素炎等の熱により反応させている、
この反応により生成されたガラス微粉末をターゲット先
端に順次堆積させ、その桑先端の温1哀分布により最終
ガラスの半径方向の屈折率分布を制ill L、、てい
る。このため、第先端部分の温度の制御は、その光フア
イバ母材から製作される光フン・イバの伝送特性、特に
、マルヂモードグレーデイド型光ファイバの伝送帯域特
性に大さな影響を及ぼすことにイヱる。Generally, a method for manufacturing optical fiber mother H by VAD method 4J
There is a significant difference in productivity. Then, raw gas such as silicon chloride (S!Cf' 4 ), which becomes the base glass, and germanium chloride (GeCj!t) and chloride oxide P'l (P OC = 1) to control the refractive index.
etc. are reacted with the heat of an oxyhydrogen flame, etc.,
The glass fine powder produced by this reaction is sequentially deposited on the tip of the target, and the temperature distribution at the tip of the target controls the radial refractive index distribution of the final glass. Therefore, controlling the temperature of the first tip has a large effect on the transmission characteristics of optical fibers made from the optical fiber base material, especially on the transmission band characteristics of multimode graded optical fibers. I especially like it.
従来、ごの最先端部分の11拍条件を−・定に調節ザる
方d、は、名種提案され、例えば、最先端部の反応温度
制御に関しては、現在±1〜2℃の範囲に調節する技術
はほぼ確立し、特性の再現性もよ・(なってさている。Conventionally, methods for adjusting the 11-beat conditions at the leading edge of the gas to a constant level have been proposed, and for example, for controlling the reaction temperature at the leading edge, it is currently within the range of ±1 to 2°C. The adjustment technology has almost been established, and the reproducibility of the characteristics is also good.
しかし、帯域特性の再現性の向上、広セ1)域フIイバ
の歩留り向上ど3っだ点からは、まだまだ問題点が多く
必ずしも満足のできる結果どはなっていない。However, there are still many problems in improving the reproducibility of band characteristics and improving the yield of wide area fibers, and the results are not necessarily satisfactory.
本発明は、上記の状況に鑑みなされたものであり、?ル
ヂモードグレーデイド型光ファイバの帯域特性の再現性
、広帯域フッ・イバの歩留りを大幅に向上できる光フア
イバ母材の製造方法を提供することを目的としたもので
ある。The present invention has been made in view of the above situation. The object of the present invention is to provide a method for manufacturing an optical fiber base material that can significantly improve the reproducibility of the band characteristics of a radial mode graded optical fiber and the yield of broadband fibers.
[発明の概要]
本光1117の光ファイバは材の製造方法は、酸素及び
水素を酸水素バーナに送入し燃焼する酸水素炎rl+
’t’ )7A化珪累及び塩化ゲルマニウム等の原料ガ
スを反応させてガラス微粉末を生成し、該ガラス微わ)
末をターグツ1−先端に推(iさせて、多孔質母材を形
成し、該多孔′:1m材を加熱透明化し光フアイバ1廿
材を製造する場合に、■−1に13+j石ガスの反応が
1!/ンバ内で行なわれ1犯ガラス微粉末の上記堆積が
継続される上記ブ]・ンバ内の内圧を周期的に変!11
Jさけ上記ガラス微粉末の11[槓条件を変化させるこ
とにより、上記透明化後の光ファイバ/’t]材の屈折
率分布指数αを長手方向に変化さ眩る方法である。[Summary of the Invention] The optical fiber manufacturing method of the optical fiber 1117 uses an oxyhydrogen flame rl+ in which oxygen and hydrogen are fed into an oxyhydrogen burner and burned.
't') A raw material gas such as 7A silica and germanium chloride is reacted to produce a glass fine powder, and the glass fine powder is produced.
When producing a 1-length optical fiber by pushing the end of the fiber into the tip of the target (i) to form a porous base material, and heating and transparentizing the porous 1m material, 13+j of stone gas is added to ■-1. The reaction takes place in the chamber and the accumulation of the fine glass powder continues. - Periodically change the internal pressure in the chamber!11
This is a method of changing the refractive index distribution index α of the above-mentioned glass fine powder material in the longitudinal direction.
[実施例]
以下、本発明の光フアイバ母材の製造方法を実施例を用
い第1図により説明する。第1図は実施装置の縦断面図
である。図において、1はターゲット、2はチャンバ、
3は堆積したガラス微粉末からなる多孔質母材(スート
)、4は堆積したガラス微粉末層の多孔質母材先端部で
あり、最高温度点である。5は多孔質母材3の反応温度
測定用窓、6は赤外線温度測定機、7は酸水素ガス流量
調節装置、8は石英管バーナ、9はチilンバ台。[Example] Hereinafter, the method for manufacturing an optical fiber preform of the present invention will be explained using an example and FIG. 1. FIG. 1 is a longitudinal sectional view of the implementation device. In the figure, 1 is the target, 2 is the chamber,
3 is a porous base material (soot) made of deposited glass fine powder, and 4 is the tip of the porous base material of the deposited glass fine powder layer, which is the highest temperature point. 5 is a window for measuring the reaction temperature of the porous base material 3, 6 is an infrared temperature measuring device, 7 is an oxyhydrogen gas flow rate adjustment device, 8 is a quartz tube burner, and 9 is a chamber stand.
10は排気0.11はチャンバ9内の圧力センリ゛。10 is the exhaust gas and 0.11 is the pressure sensor inside the chamber 9.
12は内圧調整装置、13は内圧調整駆動回路。12 is an internal pressure adjustment device, and 13 is an internal pressure adjustment drive circuit.
14(よ発振器である。石英管バーナ8はその中心7’
ijl ハーノからDlr Rガスの3 i C1!a
、 GeCl1i 。14 (It is an oscillator. The quartz tube burner 8 is located at its center 7'
ijl Harno to Dlr R gas 3 i C1! a
, GeCl1i.
1−)OCI! :]等を送入し、外管バーナからは酸
素及び水;);を送入し、さらにその外側には、3巾の
反j+Qi状態を調節り−るための不活性ガス(通常N
2ガス便用)吹出[lを持つ複合バーナ構造となってい
る。1-)OCI! :], etc., and from the outer tube burner, oxygen and water;
It has a composite burner structure with two gas outlets).
本実施例が従来の光フアイバ母材の″!A迄方法と責<
rるところは、多孔質母材(スート)3の堆積作栗継続
中の1京料ガスの反応を起こさせているヂt・シバ2内
の内圧を周+11J的に変動さぼることによ−)て、ガ
ラス微粉末1■積条件に周期的変化を与える魚である。This example describes the method and responsibility of the conventional optical fiber base material.
This is done by reducing the internal pressure within the chamber 2, which is causing the reaction of the 1000,000 yen raw material gas during the deposition of the porous base material (soot) 3, by a circumferential increase of +11 J. ), it is a fish that gives periodic changes to the volume conditions of one glass fine powder.
そして、石英バーナ管8に対して原料ガス、酸素及び水
素、及びその他のガスを送入し口11石カスを酸水素炎
中で反応さけ1回Φλづるターフット1の先端に順次カ
ラス微彰)末の堆積層を生成さ−せイ1がら徐々に引き
上げる操作により多孔?T t* (Δ3を形成させる
。一方、燃焼に用いられた酸、);及び水素、))&ひ
に反応調節に用いられたアルゴン、窒素淳のガス、ある
いは精製されたガラス(λ′(沙)末の一部’、r;
4.L lノ1気ロ10から1ノ1出される。Then, the raw material gas, oxygen, hydrogen, and other gases are fed into the quartz burner tube 8, and the stone scum is reacted in an oxyhydrogen flame at the port 11, and the tip of the turret 1, which is passed through the Φλ once, is exposed to the tip of the turret 1. A porous layer is created by gradually pulling up the final layer of sediment. T t* (Δ3 is formed; on the other hand, the acid used in the combustion, ); and hydrogen, )) & the gas of argon, nitrogen, or purified glass ( part of the end', r;
4. L No 1 Ki Ro 10 to 1 No 1 issued.
通常の条件では、酸素は8 、5f!/min 、水素
は’1.5J/min程度の流量が用いられ、さらに、
水素の流量(よターゲット1に堆積されるガラス微粒子
の層の多孔質母材先端部4の最高温度点の温度が1.0
20℃になるように調iされている。Under normal conditions, oxygen is 8,5f! /min, hydrogen is used at a flow rate of about 1.5 J/min, and further,
The flow rate of hydrogen (if the temperature at the highest temperature point of the porous base material tip 4 of the layer of glass particles deposited on the target 1 is 1.0
The temperature is adjusted to 20°C.
また、反応チャンバ2内のに内圧は圧力センナ(内圧測
定器)11により測定され、内圧調整駆動回路13を介
して内圧調整装置12を駆動することにより、通常、室
内圧力に比べて1.0mmHzOだけ低い値に一定に保
たれている。In addition, the internal pressure in the reaction chamber 2 is measured by a pressure sensor (internal pressure measuring device) 11, and by driving the internal pressure adjustment device 12 via the internal pressure adjustment drive circuit 13, the internal pressure is normally adjusted to 1.0 mmHzO compared to the indoor pressure. is kept constant at a low value.
第2図は、横軸に各波長における屈折率分布指数αをと
り、縦軸に帯域をとって両者の関係が示される日本電信
電話公社の研究実用化報告第29巻台2号(1980年
)rl、3μm帯域グレーディトを光ファイバの製作技
術」に発表された理論計q式から導からだグラフである
。第2図において、実線の曲線は0.82μn〕の波長
1点線の曲線は1.2μmの波長である。図からし分る
J:うに、各波長で広帯域どなる屈折率分布指数αの範
囲は非常に狭く、ざらに、7.i+波長と超波長のオプ
アインムl+Cjが少しく J’れているため、それぞ
れれの波長帯での広帯域化は勿論、両波ども広帯域をね
らう、いわゆるダブルウィンドウタイプの製造の再現性
向上がいかに困ツバであるか准察できる。Figure 2 shows the refractive index distribution index α at each wavelength on the horizontal axis and the band on the vertical axis to show the relationship between the two. ) rl, 3 μm band grade is a graph derived from the theoretical equation q published in ``Optical Fiber Manufacturing Technology''. In FIG. 2, the solid line curve has a wavelength of 0.82 μm, and the dotted line curve has a wavelength of 1.2 μm. It can be seen from the figure that the range of the refractive index distribution index α is very narrow and roughly 7. Since the optics of the i+ wavelength and the ultra-wavelength l+Cj are slightly different from each other, it is difficult to improve the reproducibility of so-called double-window type manufacturing, which aims to widen both wavelength bands, as well as to widen each wavelength band. I can guess whether it is.
本実施例では、発(辰’a 171からの電気信号を約
2分周期て゛振動させ、チ1!ンバ2内の内圧を、室内
圧力に比し、−1,0〜−3,0mmHz Oの範囲で
周期変動さILることにJ:す、長手方向に屈折率分布
指数(χの変動している多孔質母材(スート)3を製造
した。そして、この多孔質母材3は、屈折子分イ11指
故αが±0.05の範囲で長手方向に変動していること
が実験により確認されている。In this embodiment, the electric signal from the generator (Tatsu'a 171) is vibrated at a period of approximately 2 minutes, and the internal pressure inside the chamber 2 is -1.0 to -3.0 mmHz O compared to the indoor pressure. A porous base material (soot) 3 was manufactured in which the refractive index distribution index (χ) was varied in the longitudinal direction with a periodic variation in the range of . It has been confirmed through experiments that the refractive index α varies within a range of ±0.05 in the longitudinal direction.
上記のようにして’FFJ mした光フアイバ母材から
製作された光ファイバは、約200〜300mの周期で
長手方向に屈折率分布指数αが変化している筈であるが
、これを500m程度に切断して長手方向の帯域特性変
化を調べたところ、変動幅も小さく、かつ、広帯域とな
る割合も大幅に向上することが判明した。特に、長短両
用型のダブルウインドタイブフ?イバの歩留りは大幅に
向上し、ざらに、長距離伝送における帯域の劣化指数(
γ:0.5≦γ≦1)も従来品よりら小さ目になり、長
距離伝送にも好適であることが判明した。また、帯域特
性以外の各特性、例えば、接続時の10失特性、耐応力
特性、温度特性及び常温にd3りる1ξ1失特性等は従
来品とほとんど差のないこともに’ft 認されている
。The optical fiber manufactured from the optical fiber base material subjected to 'FFJ m' as described above should have a refractive index distribution index α changing in the longitudinal direction at a period of about 200 to 300 m, but this When we examined the change in band characteristics in the longitudinal direction by cutting into sections, we found that the fluctuation range was small and the proportion of broadband characteristics was significantly improved. In particular, a double wind tie bouffe that can be used both long and short? The yield of fiber optics has been significantly improved, and the bandwidth deterioration index for long-distance transmission (
It was also found that γ: 0.5≦γ≦1) was smaller than that of conventional products, making it suitable for long-distance transmission. In addition, it has been recognized that there is almost no difference in characteristics other than band characteristics, such as 10 loss characteristics during connection, stress resistance characteristics, temperature characteristics, and 1ξ1 loss characteristics at room temperature, compared to conventional products. There is.
一方、長手方向に屈折率分布指数αか変動しているマル
チモードグレーディト型光ファイバにおいては、各モー
ドを伝播する光ファイバが容易にカップリングを起こし
、1−一タル的なモード間の理延時間差が縮少され広帯
域化が計れることはよく知られでいる。しかし、ターゲ
ット先端部の温度等を精度よく一定にコントロールした
場合、その他の製造条件の微妙な違いにより、却って、
屈折率分布指数αを目標値とずれた所で一定にコントロ
ールすることになり、8i端に狭帯域なフフ?イバどな
る場合がよくあった。また、長手方向の帯域特性のばら
つきも大ぎいものかあつlこ1.木実1商例の方法によ
れば、屈折重分/li指数αが一定にずれることはなく
、多少ずれた場合においてすら、屈折(′コ分布指数α
が周期変動しているため極端なき火帯11戊どなること
はなくなる。On the other hand, in a multi-mode graded optical fiber in which the index of refraction α varies in the longitudinal direction, the optical fiber propagating each mode easily causes coupling, and the uni-integral relationship between the modes increases. It is well known that the delay time difference can be reduced and a wider band can be achieved. However, even if the temperature at the tip of the target is precisely controlled to a constant level, due to subtle differences in other manufacturing conditions,
The refractive index distribution index α is controlled to be constant at a point where it deviates from the target value, and a narrow band appears at the 8i end. Iba often yelled. Also, the variation in band characteristics in the longitudinal direction is also large. According to the method of Kinomi 1, the refraction weight/li index α does not deviate to a constant value, and even when it deviates slightly, the refraction ('ko distribution index α
Because of the periodic fluctuations, there will be no more extreme blazes.
この1」;うに本実施例の光フアイバ母材の製造方法に
よれば、ヂレンバ内の内圧を周期的に変動させガラス微
粉末のHt、 vi条件を変動させることにより透明化
後の光フアイバ母材の屈折率分布指数αを長手方向に変
化けることができ、帯域特性におい−C広帯域となるフ
ァイバの歩留りが大幅に向上し、また、帯域特性の長手
方向変化が少イgくなる。According to the method for manufacturing the optical fiber preform of this embodiment, the optical fiber preform after being made transparent is produced by periodically varying the internal pressure in the dilenver and varying the Ht and vi conditions of the fine glass powder. The refractive index distribution index α of the material can be varied in the longitudinal direction, and the yield of fibers with -C broadband characteristics is greatly improved, and longitudinal changes in the band characteristics are reduced.
42iに、長短両用型のファイバの歩留りについては大
幅に向上し、さらに、長尺伝送になるに従って劣化する
帯域特性の指数γが従来品より小さくなり艮7111h
il伝送に好適である。42i, the yield of both long and short-purpose fibers has been significantly improved, and the band characteristic index γ, which deteriorates as the length of transmission increases, is smaller than that of conventional products, making it 7111h.
Suitable for il transmission.
「発明の効果」
以上記述した如く本発明の光ファイバ母材の製迄方71
.によれば、マルチモードグレーディト型光ファイバの
帯域14性の再現性及び広帯域ファイバの歩留りを大幅
に向上できる効果を有づるものである。"Effects of the Invention" As described above, the method for manufacturing the optical fiber preform of the present invention 71
.. According to this method, the reproducibility of band 14 characteristics of multimode graded optical fibers and the yield of wideband fibers can be significantly improved.
第1図は本発明の光)j・イバ母IJのの製造方法を実
施する装置の新面図、第2図は日本電信電話公社の研究
実用化報告に発表された各波長にi13りる屈折率分布
指数αと帯域との関係を表ねり理論計算式のグラフであ
る。
1・・・ターゲット、2・・・チ1!ンバ、3・・・多
孔7′TL1 月。
8・・・石英管バーナ、11・・・圧力センサ、12・
・・内圧調整装置、13・・・内圧調整駆動回路。
修 V ≠Figure 1 is a new view of a device for carrying out the method of manufacturing IJ of the present invention, and Figure 2 is a new view of the equipment for implementing the method of manufacturing IJ of the present invention. It is a graph of a theoretical calculation formula showing the relationship between the refractive index distribution index α and the band. 1...Target, 2...Chi1! Nba, 3... Porous 7'TL1 month. 8...Quartz tube burner, 11...Pressure sensor, 12...
...Internal pressure adjustment device, 13...Internal pressure adjustment drive circuit. Shu V ≠
Claims (3)
水素炎中で塩化珪素及び塩化ゲルマニウム等の原料ガス
を反応させてガラス微粉末を生成し該ガラス微粉末をタ
ーゲット先端に堆積させて多孔質母材を形成し、該多孔
質母材を加熱透明化し光ファイバ母材を製造する方法に
おいて、上記原料ガスの反応がチャンバ内で行なわれ上
記ガラス微粉末の上記堆積が継続される上記チャンバ内
の内圧を周期的に変動させ上記ガラス微粉末の推積条件
を変化させることにより、上記透明化後の光ファイバ母
材の屈折率分布指数αを長手方向に変化させることを特
徴とする光ファイバ母材の製造方法。(1) Oxygen and hydrogen are fed into an oxyhydrogen burner, and raw material gases such as silicon chloride and germanium chloride are reacted in the burning oxyhydrogen flame to generate fine glass powder, and the fine glass powder is deposited on the tip of the target. In the method of producing an optical fiber preform by forming a porous preform by heating and making the porous preform transparent, the reaction of the raw material gas is carried out in a chamber, and the deposition of the fine glass powder is continued. The refractive index distribution index α of the optical fiber preform after being made transparent is changed in the longitudinal direction by periodically varying the internal pressure in the chamber and changing the estimation conditions of the glass fine powder. A method for manufacturing an optical fiber base material.
仕上りファイバ長さ換算で500m以下となるようにす
る特許請求の範囲第1項記載の光ファイバ母材の製造方
法。(2) The period of varying the internal pressure in the chamber,
The method for manufacturing an optical fiber preform according to claim 1, wherein the length of the finished fiber is 500 m or less.
01〜±0.1とする特許請求の範囲第1項記載の光フ
ァイバ母材の製造方法。(3) The range in which the refractive index distribution index α is changed is ±0.
01 to ±0.1. The method for manufacturing an optical fiber preform according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59206935A JPS6186437A (en) | 1984-10-02 | 1984-10-02 | Manufacturing method of optical fiber base material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59206935A JPS6186437A (en) | 1984-10-02 | 1984-10-02 | Manufacturing method of optical fiber base material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6186437A true JPS6186437A (en) | 1986-05-01 |
| JPH0547489B2 JPH0547489B2 (en) | 1993-07-16 |
Family
ID=16531474
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59206935A Granted JPS6186437A (en) | 1984-10-02 | 1984-10-02 | Manufacturing method of optical fiber base material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6186437A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014500980A (en) * | 2010-11-08 | 2014-01-16 | コーニング インコーポレイテッド | Multi-core optical fiber ribbon and manufacturing method thereof |
-
1984
- 1984-10-02 JP JP59206935A patent/JPS6186437A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2014500980A (en) * | 2010-11-08 | 2014-01-16 | コーニング インコーポレイテッド | Multi-core optical fiber ribbon and manufacturing method thereof |
| US9796618B2 (en) | 2010-11-08 | 2017-10-24 | Corning Incorporated | Multi-core optical fiber ribbons and methods for making the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0547489B2 (en) | 1993-07-16 |
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