JP3663871B2 - Optical fiber preform manufacturing method - Google Patents
Optical fiber preform manufacturing method Download PDFInfo
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- JP3663871B2 JP3663871B2 JP35991097A JP35991097A JP3663871B2 JP 3663871 B2 JP3663871 B2 JP 3663871B2 JP 35991097 A JP35991097 A JP 35991097A JP 35991097 A JP35991097 A JP 35991097A JP 3663871 B2 JP3663871 B2 JP 3663871B2
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- 238000004519 manufacturing process Methods 0.000 title claims description 21
- 239000013307 optical fiber Substances 0.000 title claims description 21
- 239000011521 glass Substances 0.000 claims description 109
- 239000004071 soot Substances 0.000 claims description 67
- 230000015572 biosynthetic process Effects 0.000 claims description 59
- 238000003786 synthesis reaction Methods 0.000 claims description 59
- 239000002994 raw material Substances 0.000 claims description 54
- 239000000463 material Substances 0.000 claims description 49
- 239000010419 fine particle Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 11
- 238000003466 welding Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 7
- 238000000151 deposition Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000005253 cladding Methods 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000012544 monitoring process Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000005049 silicon tetrachloride Substances 0.000 description 2
- 229910003902 SiCl 4 Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- 230000002194 synthesizing effect Effects 0.000 description 1
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Description
【0001】
【発明の属する技術分野】
本発明は、均質な光ファイバ母材を精度よく製造することができる光ファイバ母材の製造方法に関する。
【0002】
【従来の技術】
従来、コア及びクラッドからなるコア母材の両端部にダミーロッドを溶着して作製した出発部材を、軸回りに回転させながら軸方向にガラス微粒子合成用バーナに対し相対的に往復移動させ、ガラス微粒子合成用バーナで合成されたガラス微粒子を出発部材の外周に吹き付けて堆積させて光ファイバ母材を製造する方法が行われている。
この方法を実施するための装置構成の1例を図1に模式的に示す。図1の例では容器1にバーナ2を固定しておき、昇降装置4により出発部材3を回転させながら上下方向に往復移動させる。バーナ2には原料供給装置5からSiCl4 などのガラス原料及び燃焼用ガスが供給され、合成されたガラス微粒子が出発部材3の外周に堆積し、スス体(ガラス微粒子堆積体)6が形成される。
【0003】
この方法においては、出発部材3の中央側から相対移動したバーナ2がコア部材とダミーロッドとの接合部に達した時点でバーナ2へのガラス原料の供給を停止し、バーナ2はさらにダミーロッド側に移動させてガラス原料供給停止点よりも外側に形成されるスス体の端部(外径が減少する部分)の加熱を行うようにするか、あるいはバーナ2としてガラス原料を供給してガラス微粒子を合成するバーナ(ガラス合成用バーナ)の相対移動方向の前後に加熱のみを行う補助バーナを備えたバーナを使用し、ガラス合成用バーナがコア部材とダミーロッドとの接合部に達した時点でバーナを折り返し、スス体の端部は補助バーナで加熱するようにしている。
【0004】
このような方法によりスス体の形成(光ファイバ母材の製造)を行う場合、形成されるスス体の形状は図2のようになる。すなわち、出発部材3のコア部材9とダミーロッド10との接合部8を原料供給停止点(補助バーナを使用する場合はガラス合成用バーナの折り返し点)11及び12とした場合、スス体外周▲1▼(図の13)のようにスス体の外径が小さい場合には、スス体の外径定常部の長さ(透明化した際に安定した焼結体が得られる有効部の長さ)は図のa1 のようにコア母材9の長さに近いものが得られるが、スス体外周▲2▼(図の14)のように外径が大きくなるにしたがって図のa2 のようにスス体の外径定常部の長さが短くなってくる。これは原料を停止する位置は外径非定常部になるので、停止する位置でのスス粒子の流れは出発部材の中心軸に平行ではなく、傾いているためである。この場合、コア母材の端部が有効に利用されないことになり、コスト上昇の原因となる。
【0005】
以上、1個のガラス合成用バーナを使用する場合について説明したが、出発部材の中心軸に平行に配置された複数のガラス合成用バーナを使用する場合にも同様な問題がある。このような複数のガラス合成用バーナを使用する例として特開昭63−310745号公報に開示された技術がある。この技術は複数のバーナを使用し、ガラス微粒子堆積体の端部においてもガラス原料の供給を停止することなく折り返すようにした場合に生じる、ガラス微粒子堆積体端部における密度の不均一性をなくしてガラス破損のない高品質のものを大量生産することを目的としたもので、複数個のガラス発生源を用いる際に予め堆積されるターゲットの2点に標点を付しておき、トラバースされる複数個のガラス発生源のうち標点を通りすぎたものは直ちに検出手段が作動してガラス原料の供給を停止させるようにしたものである。この方法によれば、端部における複数のガラス合成用バーナ(ガラス発生源)の干渉によるスス体密度の不均質化等の問題を解決する効果はあるが、前記のようなスス体の外径の増加につれてスス体の外径定常部(有効部)の長さが短くなるという問題は依然として残されている。
【0006】
このようなスス体の外径が大きくなるにつれて外径定常部の長さが短くなり、コア母材に無駄が生じるのを防ぐためには、ガラス合成用バーナへのガラス原料供給停止点又はバーナの折り返し点を、コア母材とダミーロッドとの接合部からダミーロッド側に十分離れた位置にすればよいが、その場合にはガラス原料のロスが多くなり経済的ではない。
【0007】
【発明が解決しようとする課題】
本発明はこのような従来技術の実状に鑑み、コア母材の全長にわたって、均一な品質の外径定常部が形成されたスス体(ガラス微粒子堆積体)が得られ、ガラス原料の損失も少ない光ファイバ母材の製造方法を提供しようとするものである。
【0008】
【課題を解決するための手段】
本発明は上記課題を解決する手段として、次の(1)〜(4)の態様を有するものである。
(1)コア及びクラッドからなるコア母材の両端部にダミーロッドを溶着して作製した出発部材を、軸回りに回転させながら軸方向にガラス合成用バーナに対し相対的に往復移動させ、ガラス合成用バーナで合成されたガラス微粒子を出発部材の外周に吹き付けて堆積させる方法であって、ガラス合成用バーナの相対移動方向の前後に加熱のみを行う補助バーナを備えた一個のバーナを使用し、コア母材側からダミーロッド側へ相対移動するガラス合成用バーナは前記コア母材とダミーロッドとの接合部で折り返し、スス体の端部は補助バーナで加熱するようにしてスス付けを行う光ファイバ母材の製造方法において、ガラス合成用バーナの折り返し位置をスス体の外径が大きくなるに応じて、コア母材とダミーロッドとの接合部からダミーロッド側に移動させることを特徴とする光ファイバ母材の製造方法。
【0009】
(2)コア及びクラッドからなるコア母材の両端部にダミーロッドを溶着して作製した出発部材を、軸回りに回転させながら軸方向にガラス合成用バーナに対し相対的に往復移動させ、ガラス合成用バーナで合成されたガラス微粒子を出発部材の外周に吹き付けて堆積させる方法であって、一個のガラス合成用バーナを使用し、コア母材側からダミーロッド側へ相対移動するガラス合成用バーナが前記コア母材とダミーロッドとの接合部に達した時点でガラス合成用バーナへの原料供給を停止し、該原料供給を停止したガラス合成用バーナをさらにダミーロッド側に移動させてスス体の端部を加熱し、折り返したガラス合成用バーナが前記接合部に達した時点で原料供給を開始するようにしてスス付けを行う光ファイバ母材の製造方法において、ガラス合成用バーナへの原料供給停止及び開始位置をスス体の外径が大きくなるに応じて、コア母材とダミーロッドとの接合部からダミーロッド側に移動させることを特徴とする光ファイバ母材の製造方法。
【0010】
(3)コア及びクラッドからなるコア母材の両端部にダミーロッドを溶着して作製した出発部材を、軸回りに回転させながら軸方向にガラス合成用バーナに対し相対的に往復移動させ、ガラス合成用バーナで合成されたガラス微粒子を出発部材の外周に吹き付けて堆積させる方法であって、出発部材の中心軸に平行に配置された複数のガラス合成用バーナを使用し、コア母材側からダミーロッド側へ相対移動する複数のガラス合成用バーナが順次前記コア母材とダミーロッドとの接合部に達した時点でガラス合成用バーナへの原料供給を停止し、該原料供給を停止したガラス合成用バーナでスス体の端部を加熱し、折り返した各ガラス合成用バーナが前記接合部に達した時点で原料供給を開始するようにしてスス付けを行う光ファイバ母材の製造方法において、ガラス合成用バーナへの原料供給停止及び開始位置をスス体の外径が大きくなるに応じて、コア母材とダミーロッドとの接合部からダミーロッド側に移動させることを特徴とする光ファイバ母材の製造方法。
【0011】
(4)前記複数のガラス合成用バーナのうちの最も出発部材の中央側に位置するバーナがガラス合成用バーナへの原料供給停止及び開始位置に達した時点でガラス合成用バーナを折り返すようにし、その時点で前記最も出発部材の中央側に位置するバーナへの原料供給は停止しないようにすることを特徴とする前記(3)の光ファイバ母材の製造方法。
【0012】
【発明の実施の形態】
本発明の方法は、スス体の外径が大きくなるのに応じてガラス原料の供給範囲をコア母材とダミーロッドとの接合部(以下、単に接合部と称する)からダミーロッド側へ徐々に広げていくことを特徴とする。
すなわち、前記(1)の発明においてはガラス合成用バーナの折り返し点を、前記(2)及び(3)の発明においてはガラス合成用バーナへのガラス原料の供給停止又は開始位置を、前記(4)の発明においては最も中央寄りのガラス合成用バーナ(往復移動の両端部において最も内側に位置するガラス合成用バーナ)の折り返し点であり、かつ、その他のガラス合成用バーナへのガラス原料の供給停止又は開始位置を、スス体の外径が大きくなるのに応じて接合部からダミーロッド側へ徐々に移動させるようにする。
【0013】
スス体の外径定常部(この部分が均質で良好な特性を有するファイバが得られる有効部となる)の長さは、スス体の外径が一定であればほぼ一定となるが、外径が大きくなるにしたがって外径非定常部が前記ガラス原料停止等の位置の前後方向に広がり、外径定常部の長さが短くなってくる。すなわち、ガラス原料停止等の位置を接合部とした場合には、外径が大きくなるにつれて外径定常部の端部が接合部から徐々にコア母材の中央側にずれてくる。そのため本発明においては、スス体の外径をモニターしながらスス付けを行い、予め経験的に求められたスス外径と外径定常部の長さ変動との関係からコンピューター制御等により、前記のずれの大きさに相当する長さだけガラス原料停止等の位置を接合部からダミーロッド側に移動させるようにする。これにより、外径の寸法にかかわらず、ほぼコア母材の全長にわたって外径定常部を形成させることができる。
【0014】
なお、使用するガラス合成用バーナの本数は、目的とする製品の大きさ等によって適宜定めればよいが、複数本使用する場合には装置の形状、効率等から3〜4本とするのが好ましい。また、安定した火炎状態を維持するため、ガラス合成用バーナへの原料供給の停止及び再開は瞬間的に行うのではなく、数秒〜10秒程度をかけて行うようにするのが好ましい。
【0015】
【実施例】
以下実施例により本発明の方法をさらに具体的に説明する。
(実施例1)
図1の構成の装置を使用してスス付けを行い、スス外径と外径定常部の長さとの関係を調べた。コア/クラッド部を有する直径30mmのガラスロッド(コア母材)を500mm用いて両側に石英ガラス製ダミーロッドを溶着して出発部材を作製し、そのロッドを40rpmで回転しながら鉛直方向に把持し、上下に往復運動させながらガラス微粒子合成用バーナから生成するガラス微粒子を順次積層させてガラス微粒子堆積体(スス体)を作製した。バーナは同心円状8重管構造のものを用い、出発部材の回転軸に対して垂直に配置した。バーナには原料となる四塩化珪素:3slm(スタンダードリットル/分)を供給し、火炎を形成するための水素:60slm及び酸素:45slm、さらにシールガスとしてAr:4slmを供給した。
また、本構成のバーナに加え、バーナの移動方向の両側にそれぞれ200mmの間隔で同心円状の2重管構造の補助バーナを取付け、酸素:10slm及び水素:30slmを供給してスス体端部を加熱するようにした。
【0016】
バーナが出発部材のコア母材とダミーロッドとの接合部の位置にきたとき、出発部材のトラバースの向きを変えるようにし、このように往復トラバースを継続しつつ、スス外径がそれぞれ100、150、220、250mmになるまでスス付けを継続した。このようにして得られたそれぞれのスス体を高温にした炉で透明化した後、ファイバ化し、カットオフ波長、MFD(モードフィールド径)などのファイバ特性を調べたところ、スス体の外径が大きくなるにつれて、両端の特性が安定しない部分(外径非定常部に相当)と特性の安定した部分(外径定常部に相当)との境界点、すなわち有効部の端部がコア母材とダミーロッドとの接合部からコア母材中央側にずれてきており、図3に示す相関図が得られた。
【0017】
このコア母材を500mm使用して前記と同じ条件でスス付けを行った。スス付け中はスス外径をモニターし、図3のデータに基づいてそのときのスス外径に応じてトラバースの折り返し位置を接合部からダミーロッド側に徐々に移動させた。このようにして、外径がこのコア母材のコア/クラッド比から算出した目標値である150mmになるまでスス付けを行いガラス微粒子堆積体(スス体)を得た。最終的にトラバースの折り返し点は接合部からダミーロッド側に50mmずれた位置となった。得られたスス体を高温の炉により透明化し、外径80mmの良好な透明度を有し、表面や内部のクラック、突起、異物などが認められない品質良好な焼結体を得た。この焼結体をファイバ化し、カットオフ波長、MFDなどのファイバ特性を調べたところ、全長にわたり良好であった。
【0018】
(実施例2)
実施例1と同じコア母材を500mm使用して前記と同じバーナ条件でスス付けを行った。この例では補助バーナは使用せず、ガラス合成用バーナが出発部材のコア母材とダミーロッドとの接合部の位置にきたときにバーナへの原料供給を停止し、さらに同方向への移動を続けて火炎のみによりスス体の端部を加熱するようにした。バーナが原料供給停止位置から200mmの位置に達した時点でバーナを折り返し、原料供給停止位置へ戻った時点でバーナへの原料供給を再開した。
以降はスス外径をモニターしながら、図3のデータに基づいてそのときのスス外径に応じてバーナへの原料供給停止及び再開位置を接合部からダミーロッド側へ徐々に移動させ、外径150mmになるまでスス付けを行った。最終的に原料供給停止及び再開位置は接合部からダミーロッド側に50mmずれた位置となった。得られたスス体を高温の炉で透明化した焼結体の品質は良好で、ファイバ特性も全長にわたり良好であった。
【0019】
(実施例3)
実施例1で使用したものと同一のコア母材500mmを用いて両側に石英ガラス製ダミーロッドを溶着して出発部材を作製し、図1の構成の装置により、そのロッドを40rpmで回転しながら鉛直方向に把持し、上下に往復運動させながらガラス微粒子合成用バーナから生成するガラス微粒子を順次積層させることによりガラス微粒子堆積体(スス体)を作製した。この例においては同心円状8重管構造のバーナを3本用い、出発部材の回転軸に対して垂直でかつ3本のバーナはお互いに平行で等間隔(200mm間隔)となるように配列した。各バーナには原料となる四塩化珪素:3slmを供給し、火炎を形成するための水素:60slm及び酸素:45slm、さらにシールガスとしてAr:4slmを供給した。
【0020】
往復トラバースを行い、バーナ群が出発部材の一方の端部に近づいた際に、1、2本目のバーナについてはバーナが順次所定の位置に到達したらコンピュータ制御によりそのバーナへのガラス原料供給を停止し、さらに同方向への移動を続けて火炎のみによりスス体の端部を加熱するようにした。3本目のバーナが所定の位置に到達したら原料の供給は停止せずに折り返して逆方向にトラバースし、2本目及び1本目のバーナが順次所定の位置に戻った時点でそれぞれのバーナへのガラス原料供給を再開した。このパターンをコア母材の両端(反対側の端部ではバーナの順番が逆転する)で行い、外径がこのコア母材のコア/クラッド比から算出した目標値である150mmになるまでスス付けを行いガラス微粒子堆積体(スス体)を得た。
【0021】
前記所定位置(1、2本目のバーナへの原料供給停止及び開始点、かつ、3本目のバーナの折り返し点)は、スス付け開始時点は接合部とし、以降はスス外径をモニターしながら図3のデータに基づいてそのときのスス外径に応じて前記所定位置を接合部からダミーロッド側に徐々に移動させた。最終的に前記所定位置は接合部からダミーロッド側に50mmずれた位置となった。
このようにして得られたスス体を高温の炉により透明化し、外径82mmの良好な焼結体を得た。この焼結体をファイバ化し、カットオフ波長、MFDなどのファイバ特性を調べたところ、全長にわたり良好な特性が得られた。
【0022】
(比較例1)
1、2本目のバーナへの原料供給停止及び開始点、かつ、3本目のバーナの折り返し点となる所定位置を接合部に固定した外は実施例2と同様に操作し、外径が150mmのスス体を作製した。得られたスス体を高温にした炉で透明化し、外径81mmの良好な焼結体を得た。ところがこの焼結体を線引炉でファイバ化し、カットオフ波長、MFDなどのファイバ特性を調べたところ、両端の接合部からそれぞれ49mm及び48mmの範囲までカットオフ波長、MFDなどの特性が狙いの値から徐々にずれていることがわかった。
【0023】
【発明の効果】
合成中のスス体の外径に合わせてコア母材端部近傍におけるガラス合成用バーナへの原料供給停止及び再開位置又は原料供給を停止しないバーナの折り返し位置を、コア母材とダミーロッドとの接合部からダミーロッド側(コア母材の外側)へ徐々に移動させることによって、スス外径が大きい場合でもコア母材の全長にわたって特性の安定した光ファイバが得られる外径定常部(有効部)が形成された光ファイバ母材(スス体)を得ることができる。
【図面の簡単な説明】
【図1】ガラス微粒子合成用バーナを使用した光ファイバ母材製造装置の構成例を模式的に示す図。
【図2】スス体形成時のスス外径により外径定常部の長さの変化の状態を説明する図。
【図3】実施例1における有効部端部位置の、接合部からのずれの大きさとスス外径との関係を示す相関図。
【符号の説明】
1 容器 2 バーナ 3 出発部材 4昇降装置
5 原料供給装置 6 スス体 8 接合部 9 コア母材
10 ダミーロッド 11,12 原料供給停止点
13 スス体外周▲1▼ 14 スス体外周▲2▼[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method of manufacturing an optical fiber preform that can accurately manufacture a homogeneous optical fiber preform.
[0002]
[Prior art]
Conventionally, a starting member produced by welding a dummy rod to both ends of a core base material consisting of a core and a clad is reciprocated relative to the glass particle synthesis burner in the axial direction while rotating around the axis, and glass There is a method of manufacturing an optical fiber preform by spraying and depositing glass fine particles synthesized by a fine particle synthesizing burner on the outer periphery of a starting member.
An example of an apparatus configuration for carrying out this method is schematically shown in FIG. In the example of FIG. 1, the
[0003]
In this method, when the
[0004]
When forming a soot body (manufacture of an optical fiber preform) by such a method, the shape of the soot body is as shown in FIG. That is, when the joint 8 between the core member 9 of the starting member 3 and the dummy rod 10 is the raw material supply stop points (when the auxiliary burner is used, the folding point of the glass synthesis burner) 11 and 12, the outer periphery of the soot body ▲ When the outer diameter of the soot body is small as in 1 ▼ (13 in the figure), the length of the outer diameter steady portion of the soot body (the length of the effective portion that provides a stable sintered body when transparent) ) Can be obtained near the length of the core base material 9 as shown in a1 in the figure, but as shown in a2 in the figure as the outer diameter increases as shown in the outer periphery of the soot body (2) (14 in the figure). The length of the outer diameter stationary part of the soot body becomes shorter. This is because the soot particle flow at the position where the raw material is stopped is not parallel to the central axis of the starting member but is inclined because the position where the raw material is stopped is an unsteady outer diameter portion. In this case, the end portion of the core base material is not effectively used, which causes an increase in cost.
[0005]
As described above, the case of using one glass synthesis burner has been described, but there is a similar problem when using a plurality of glass synthesis burners arranged in parallel to the central axis of the starting member. As an example of using such a plurality of glass synthesis burners, there is a technique disclosed in Japanese Patent Laid-Open No. 63-310745. This technology uses multiple burners and eliminates the non-uniformity of density at the end of the glass particulate deposit that occurs when the end of the glass particulate deposit is folded back without stopping the supply of glass material. The purpose is to mass-produce high-quality products that are not damaged by glass. Two or more targets deposited in advance when using multiple glass sources are marked and traversed. Among the plurality of glass generation sources, the one that passes the gauge point is one in which the detection means is immediately activated to stop the supply of the glass raw material. According to this method, there is an effect of solving problems such as non-homogeneous soot density due to interference of a plurality of glass synthesis burners (glass generation sources) at the end, but the outer diameter of the soot body as described above. There remains a problem that the length of the outer diameter steady portion (effective portion) of the soot body becomes shorter with an increase in the soot body.
[0006]
As the outer diameter of the soot body increases, the length of the outer diameter steady portion decreases, and in order to prevent the core base material from being wasted, the glass raw material supply stop point to the glass synthesis burner or the burner The turning point may be set at a position sufficiently away from the joint portion between the core base material and the dummy rod toward the dummy rod, but in this case, the loss of the glass raw material increases, which is not economical.
[0007]
[Problems to be solved by the invention]
In the present invention, in view of such a state of the prior art, a soot body (glass fine particle deposit) having a uniform quality outer diameter portion formed over the entire length of the core base material is obtained, and the loss of the glass raw material is small. An object of the present invention is to provide a method for manufacturing an optical fiber preform.
[0008]
[Means for Solving the Problems]
The present invention has the following aspects (1) to (4) as means for solving the above problems.
(1) A starting member produced by welding a dummy rod to both ends of a core base material composed of a core and a clad is reciprocated relative to the glass synthesis burner in the axial direction while rotating around the axis, and glass A method of spraying and depositing glass fine particles synthesized by a synthesis burner on the outer periphery of a starting member, using a single burner equipped with an auxiliary burner that only performs heating before and after the relative movement direction of the glass synthesis burner. The glass synthesis burner that moves relatively from the core base material side to the dummy rod side is folded at the joint between the core base material and the dummy rod, and the end of the soot body is heated by the auxiliary burner for sooting. In the method of manufacturing the optical fiber preform, the folding position of the glass synthesis burner is changed from the joint between the core preform and the dummy rod to the dummy position as the outer diameter of the soot body increases. Method for manufacturing an optical fiber preform, characterized in that moving the head side.
[0009]
(2) A starting member prepared by welding dummy rods to both ends of a core base material composed of a core and a clad is reciprocated relative to the glass synthesis burner in the axial direction while rotating around the axis, and glass A method of spraying and depositing glass fine particles synthesized by a synthesis burner on the outer periphery of a starting member, using a single glass synthesis burner, and relatively moving from a core base material side to a dummy rod side. Stops the supply of the raw material to the glass synthesis burner when it reaches the joint between the core base material and the dummy rod, and further moves the glass synthesis burner that has stopped the supply of raw material to the dummy rod side soot body In the method of manufacturing an optical fiber preform, sooting is performed so that the raw material supply is started when the end of the glass is heated and the folded glass synthesis burner reaches the joint. An optical fiber characterized in that the raw material supply stop and start position to the glass synthesis burner are moved from the joint between the core base material and the dummy rod to the dummy rod side as the outer diameter of the soot body increases A manufacturing method of a base material.
[0010]
(3) A starting member prepared by welding dummy rods to both ends of a core base material composed of a core and a clad is reciprocated relative to the glass synthesis burner in the axial direction while rotating around the axis, and glass A method of spraying and depositing glass fine particles synthesized by a synthesis burner on the outer periphery of a starting member, using a plurality of glass synthesis burners arranged in parallel to the central axis of the starting member, from the core base material side When the plurality of glass synthesis burners that move relative to the dummy rod side sequentially reach the joint between the core base material and the dummy rod, the supply of the raw material to the glass synthesis burner is stopped, and the supply of the glass is stopped. The end of the soot body is heated with a synthesis burner, and the optical fiber preform is soaked so that the raw material supply is started when each folded glass synthesis burner reaches the joint. In the manufacturing method, the raw material supply stop and start position to the glass synthesis burner is moved from the joint between the core base material and the dummy rod to the dummy rod side in accordance with the increase in the outer diameter of the soot body. An optical fiber preform manufacturing method.
[0011]
(4) The glass synthesis burner is folded when the burner located at the center side of the starting member among the plurality of glass synthesis burners reaches the starting and stopping position of the raw material supply to the glass synthesis burner, The method for producing an optical fiber preform according to (3), wherein the raw material supply to the burner located closest to the center of the starting member is not stopped at that time.
[0012]
DETAILED DESCRIPTION OF THE INVENTION
According to the method of the present invention, as the outer diameter of the soot body increases, the supply range of the glass raw material is gradually increased from the joint between the core base material and the dummy rod (hereinafter simply referred to as a joint) to the dummy rod side. It is characterized by spreading.
That is, the turning point of the glass synthesis burner in the invention of (1), the supply stop or start position of the glass raw material to the glass synthesis burner in the inventions of (2) and (3), ) Is the turning point of the most central glass synthesis burner (the innermost glass synthesis burner at both ends of the reciprocating movement) and the supply of the glass raw material to the other glass synthesis burners The stop or start position is gradually moved from the joint to the dummy rod side as the outer diameter of the soot body increases.
[0013]
The length of the outer part of the soot body (this part becomes an effective part from which a homogeneous and good fiber can be obtained) is almost constant if the outer diameter of the soot body is constant. As the diameter increases, the outer diameter non-stationary part spreads in the front-rear direction of the position of the glass raw material stop and the like, and the length of the outer diameter steady part becomes shorter. That is, when the position of the glass raw material stop or the like is a joint, the end of the outer diameter steady portion gradually shifts from the joint to the center side of the core base material as the outer diameter increases. Therefore, in the present invention, sooting is performed while monitoring the outer diameter of the soot body, and by computer control or the like from the relationship between the soot outer diameter determined in advance and the length variation of the outer diameter steady portion, The position of stopping the glass raw material is moved from the joint to the dummy rod side by a length corresponding to the size of the deviation. Thereby, regardless of the dimension of the outer diameter, the outer diameter steady portion can be formed substantially over the entire length of the core base material.
[0014]
The number of glass synthesis burners to be used may be determined appropriately depending on the size of the target product, etc., but when using a plurality of glass burners, the number should be 3 to 4 in view of the shape and efficiency of the apparatus. preferable. Moreover, in order to maintain a stable flame state, it is preferable to stop and restart the supply of the raw material to the glass synthesis burner over several seconds to 10 seconds instead of instantaneously.
[0015]
【Example】
Hereinafter, the method of the present invention will be described more specifically by way of examples.
(Example 1)
Sooting was performed using the apparatus having the configuration shown in FIG. 1, and the relationship between the soot outer diameter and the length of the outer diameter steady portion was examined. Using a glass rod (core base material) with a diameter of 30 mm having a core / cladding part, a quartz glass dummy rod is welded on both sides to prepare a starting member, and the rod is gripped in a vertical direction while rotating at 40 rpm. Then, glass fine particles generated from a glass fine particle synthesis burner were sequentially laminated while reciprocating up and down to produce a glass fine particle deposit (soot). The burner used was a concentric eight-tube structure and was arranged perpendicular to the rotation axis of the starting member. The burner was supplied with silicon tetrachloride as a raw material: 3 slm (standard liter / min), hydrogen: 60 slm and oxygen: 45 slm for forming a flame, and Ar: 4 slm as a sealing gas.
In addition to the burner of this configuration, concentric double tube auxiliary burners are attached to both sides of the burner in the moving direction at intervals of 200 mm, and oxygen: 10 slm and hydrogen: 30 slm are supplied so that the end of the soot body is It was made to heat.
[0016]
When the burner reaches the position of the joint between the core base material of the starting member and the dummy rod, the direction of the traverse of the starting member is changed, and the soot outer diameter is 100, 150 respectively while continuing the reciprocating traverse in this way. Sooting was continued until 220, 250 mm. Each of the soot bodies thus obtained was made transparent in a furnace heated to a high temperature and then made into fibers, and fiber characteristics such as cutoff wavelength and MFD (mode field diameter) were examined. As it becomes larger, the boundary point between the part where the characteristics at both ends are not stable (corresponding to the outer diameter unsteady part) and the part where the characteristic is stable (corresponding to the outer diameter steady part), that is, the end of the effective part is the core base material. It has shifted | deviated from the junction part with a dummy rod to the core base material center side, and the correlation diagram shown in FIG. 3 was obtained.
[0017]
Sooting was performed under the same conditions as described above using 500 mm of the core base material. During sooting, the soot outer diameter was monitored, and based on the data in FIG. 3, the traverse folding position was gradually moved from the joint to the dummy rod side according to the soot outer diameter at that time. Thus, sooting was performed until the outer diameter reached a target value of 150 mm calculated from the core / cladding ratio of the core base material to obtain a glass particulate deposit (soot body). Finally, the turning point of the traverse was shifted by 50 mm from the joint to the dummy rod side. The obtained soot body was made transparent by a high-temperature furnace to obtain a sintered body having a good transparency with an outer diameter of 80 mm and having no surface, internal cracks, protrusions, foreign matter, etc. This sintered body was converted into a fiber, and fiber characteristics such as cutoff wavelength and MFD were examined.
[0018]
(Example 2)
Using the same core base material as in Example 1, 500 mm, sooting was performed under the same burner conditions as described above. In this example, the auxiliary burner is not used, and when the glass synthesis burner comes to the position of the joint between the core base material of the starting member and the dummy rod, the supply of the raw material to the burner is stopped and further moved in the same direction. Subsequently, the end of the soot body was heated only by the flame. When the burner reached a position 200 mm from the raw material supply stop position, the burner was turned back, and when the burner returned to the raw material supply stop position, the supply of the raw material to the burner was resumed.
Thereafter, while monitoring the outer diameter of the soot, based on the data of FIG. 3, the raw material supply stop and restart position to the burner is gradually moved from the joint to the dummy rod side according to the outer diameter of the soot, and the outer diameter is Sooting was performed until the thickness became 150 mm. Finally, the raw material supply stop and restart positions were shifted by 50 mm from the joint to the dummy rod side. The quality of the sintered body obtained by transparentizing the obtained soot body in a high-temperature furnace was good, and the fiber characteristics were also good over the entire length.
[0019]
(Example 3)
A quartz glass dummy rod is welded to both sides using the same core base material 500 mm used in Example 1, and a starting member is produced. While rotating the rod at 40 rpm with the apparatus having the configuration shown in FIG. A glass fine particle deposit (soot body) was produced by sequentially laminating glass fine particles generated from a glass fine particle synthesis burner while vertically reciprocating and holding in a vertical direction. In this example, three burners having a concentric octuple structure were used, and the three burners were arranged so as to be perpendicular to the rotation axis of the starting member and parallel to each other at equal intervals (200 mm intervals). Each burner was supplied with silicon tetrachloride: 3 slm as a raw material, hydrogen: 60 slm and oxygen: 45 slm for forming a flame, and Ar: 4 slm as a sealing gas.
[0020]
When reciprocating traverse is performed and the burner group approaches one end of the starting member, when the burner reaches the predetermined position for the first and second burners, the glass raw material supply to the burner is stopped by computer control. Further, the end of the soot body was heated only by the flame by continuing the movement in the same direction. When the third burner reaches a predetermined position, the supply of the raw material is turned back without stopping and traversed in the reverse direction, and when the second and first burners sequentially return to the predetermined position, the glass to each burner Raw material supply resumed. This pattern is performed at both ends of the core base material (the order of the burners is reversed at the opposite end), and soot is applied until the outer diameter reaches 150 mm, which is the target value calculated from the core / cladding ratio of the core base material. To obtain a glass fine particle deposit (soot).
[0021]
The predetermined position (stopping and starting point of raw material supply to the first and second burners, and the turning point of the third burner) is a joint at the start of sooting, and thereafter, while monitoring the outer diameter of the soot. Based on the data of No. 3, the predetermined position was gradually moved from the joint to the dummy rod side according to the outer diameter of the soot. Finally, the predetermined position was shifted by 50 mm from the joint to the dummy rod side.
The soot body thus obtained was made transparent by a high-temperature furnace, and a good sintered body having an outer diameter of 82 mm was obtained. The sintered body was converted into a fiber, and fiber characteristics such as cutoff wavelength and MFD were examined. As a result, good characteristics were obtained over the entire length.
[0022]
(Comparative Example 1)
The operation was performed in the same manner as in Example 2 except that the raw material supply stop and start point to the first and second burners, and the predetermined position serving as the turning point of the third burner were fixed to the joint, and the outer diameter was 150 mm. A soot body was produced. The obtained soot body was made transparent in a furnace heated to a high temperature to obtain a good sintered body having an outer diameter of 81 mm. However, when this sintered body was made into a fiber in a drawing furnace and the fiber characteristics such as cutoff wavelength and MFD were examined, the characteristics such as cutoff wavelength and MFD from the joints at both ends to the range of 49 mm and 48 mm respectively were targeted. It was found that there was a gradual deviation from the value.
[0023]
【The invention's effect】
The raw material supply stop and restart position to the glass synthesis burner near the end of the core base material in accordance with the outer diameter of the soot body being synthesized, or the return position of the burner that does not stop the raw material supply, is determined between the core base material and the dummy rod. By moving gradually from the joint to the dummy rod side (outside of the core base material), even when the outer diameter of the soot is large, an outer diameter steady-state part (effective part) that can obtain an optical fiber with stable characteristics over the entire length of the core base material ) Can be obtained.
[Brief description of the drawings]
FIG. 1 is a diagram schematically showing a configuration example of an optical fiber preform manufacturing apparatus using a glass fine particle synthesis burner.
FIG. 2 is a diagram for explaining a state of change in the length of a constant outer diameter portion according to a soot outer diameter when forming a soot body;
FIG. 3 is a correlation diagram showing the relationship between the magnitude of deviation from the joint and the soot outer diameter at the end position of the effective portion in the first embodiment.
[Explanation of symbols]
DESCRIPTION OF
Claims (4)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35991097A JP3663871B2 (en) | 1997-12-26 | 1997-12-26 | Optical fiber preform manufacturing method |
| CNB988125536A CN1138713C (en) | 1997-12-26 | 1998-11-18 | Method and apparatus for manufacturing optical fiber base material |
| PCT/JP1998/005180 WO1999033755A1 (en) | 1997-12-26 | 1998-11-18 | Method and apparatus for manufacturing optical fiber base material |
| EP98954721A EP1044931A4 (en) | 1997-12-26 | 1998-11-18 | METHOD AND DEVICE FOR MANUFACTURING OPTICAL FIBER BASE MATERIAL |
| US10/005,199 US20020073743A1 (en) | 1997-12-26 | 2001-12-07 | Method and apparatus for making optical fiber preform |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35991097A JP3663871B2 (en) | 1997-12-26 | 1997-12-26 | Optical fiber preform manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH11189429A JPH11189429A (en) | 1999-07-13 |
| JP3663871B2 true JP3663871B2 (en) | 2005-06-22 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP35991097A Expired - Lifetime JP3663871B2 (en) | 1997-12-26 | 1997-12-26 | Optical fiber preform manufacturing method |
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| JP (1) | JP3663871B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100484752C (en) * | 2000-10-26 | 2009-05-06 | 尼奥弗托尼克斯公司 | Multilayered optical structures |
| CN116282885B (en) * | 2023-03-28 | 2024-11-12 | 江苏亨通光导新材料有限公司 | Control method for improving uniformity of cutoff wavelength and mode field diameter of optical fiber preform |
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- 1997-12-26 JP JP35991097A patent/JP3663871B2/en not_active Expired - Lifetime
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