JPS5845132A - Method and apparatus for manufacturing base material for optical fiber by vad method - Google Patents

Method and apparatus for manufacturing base material for optical fiber by vad method

Info

Publication number
JPS5845132A
JPS5845132A JP14393781A JP14393781A JPS5845132A JP S5845132 A JPS5845132 A JP S5845132A JP 14393781 A JP14393781 A JP 14393781A JP 14393781 A JP14393781 A JP 14393781A JP S5845132 A JPS5845132 A JP S5845132A
Authority
JP
Japan
Prior art keywords
base material
optical fiber
dopant
gas
starting material
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.)
Pending
Application number
JP14393781A
Other languages
Japanese (ja)
Inventor
Hideo Kakuzen
覚前 英夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries Ltd
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 by Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP14393781A priority Critical patent/JPS5845132A/en
Publication of JPS5845132A publication Critical patent/JPS5845132A/en
Pending legal-status Critical Current

Links

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]

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)

Abstract

PURPOSE:To enhance the efficiency of manufacturing a base material for an optical fiber by a VAD method by blowing a heated gas into a muffle furnace used in the manufacture to accelerate the hydrolysis of a gaseous starting material and to prevent the scattering of a dopant. CONSTITUTION:A quartz rod 1 is put in a muffle furnace 4 as a reactor, and while rotating the rod 1, H2 and O2 for forming an oxyhydrogen flame, SiCl4 as a starting material for glass and GeCl4 or the like as a dopant are blown from an oxyhydrogen burner 2. The cheorides are hydrolyzed by the intense heat of an oxyhydrogen flame formed with the burner 2 and produced H2O to form a glass layer 3 with a specified refractive index on the tip target of the rod 1 as a base material for an optical fiber. At this time, by blowing N2, CO2, air or the like into the furnace 4 from a suction hole 7 after heating with a heater 8, the internal temp. of the furnace 4 is raised and the heat of the flame is chiefly applied to the hydrolysis of the starting material, thereby preventing a reduction in the efficiency of manufacturing the base material 3 due to the scattering of GeO2 as the dopant.

Description

【発明の詳細な説明】 本発明は光ファイバーをVムク法(Vaporphas
・・axial deposition、’l気相軸付
は成長法)で製造する際の改良法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides optical fibers using the V-muk method (Vaporphas method).
...Relates to an improved method for manufacturing by axial deposition (vapor phase axial growth method).

WAD法1に第1図で具体的に説明すると、回転しなが
ら上昇する石英棒等の出発材1の先端をターゲットとし
て、酸水素バーナ−2中に、H,、0,,810ノ4 
、Ge04 、Pool@ 、 BBrl等のガスを流
し、酸水素炎中で、加水分解を起こさせて、8101 
、GeO2、p= O,% n5os等の酸化物微粒子
とする。その反応例を式で示すと次のようになる。
To explain the WAD method 1 in detail with reference to FIG. 1, H, 0,, 810 no.
, Ge04, Pool@, BBrl, etc., and caused hydrolysis in an oxyhydrogen flame to produce 8101.
, GeO2, p=O, % n5os, or the like. An example of this reaction is expressed as follows.

81ot、  +  211意0−+810茸 + 4
HC!jGfhO14+ 2H10−+G@01 + 
4107この酸化物微粒子が上記ターゲットに吹付けら
れる結果、スス体3が長さ方向に成長する。これら1.
2.3の一部または全部がマツフル4に囲まれておシ、
58はマツフル4に取り付けられて−る排気孔、またマ
ツフル4の内面に酸化物微粒子が付着するのt防ぐため
に、吸気孔6からN、ガスをマツフ#4内に流し込む。
81ot, + 211 0-+810 mushroom + 4
HC! jGfhO14+ 2H10-+G@01 +
4107 As a result of this oxide fine particle being sprayed onto the target, soot body 3 grows in the length direction. These 1.
2. Part or all of 3 is surrounded by Matsuful 4,
Reference numeral 58 denotes an exhaust hole attached to the muffler 4, and in order to prevent fine oxide particles from adhering to the inner surface of the muffler 4, nitrogen and gas are flowed into the muffler #4 from the intake hole 6.

以上が従来のWAD法および装置の概略である。The above is an outline of the conventional WAD method and device.

この方法にお−てバーナーは、酸素及び水素ガスの反応
によシ、同時にバーナーから吐出される81014 、
Ge04等のガス体の温度を上げることと、酸水素反応
により生ずるH、Oにより BiCl2、G13C14
等ガスに加水分解を行うことの2種の機能を果たしてい
る。
In this method, the burner is activated by the reaction of oxygen and hydrogen gases, which are simultaneously discharged from the burner.
BiCl2, G13C14 by increasing the temperature of gas such as Ge04 and H and O generated by oxyhydrogen reaction.
It performs two functions: to perform hydrolysis into equal gases.

しかしながら従来法で祉スス体製造効率が多少低く、ま
友安定していなかったためにGeO2の気散が起きると
いう欠点があった。本発明はWAD法におけるこのよう
な欠点を除く定めに、従来法におけるマツフル(容器)
内に加熱したN2ガス、CO,ガス、空気等の加熱ガス
を新九に、吹込んで、酸水素バーナーのガスの昇温もし
くは酸水素バーナーで形成され几炎からの熱エネルギー
放散抑制を計って、酸水素バーナーの生皮る機能を加水
分解に偏重させ、吐出ガスの昇温に対する負担を軽くし
て、スス体製造時の安定側#を可能とし、スス体合成速
度を上げ、GeO鵞の気散を防止するものである。
However, the conventional method had the disadvantage that the production efficiency of the soot body was somewhat low and that the formation of the soot was not stable, which caused GeO2 to diffuse. The present invention aims to eliminate such drawbacks in the WAD method, and to
A heated gas such as N2 gas, CO, gas, or air is injected into the new tank to raise the temperature of the gas in the oxyhydrogen burner or to suppress the dissipation of thermal energy from the flame formed by the oxyhydrogen burner. , the raw skin function of the oxyhydrogen burner is concentrated on hydrolysis, which reduces the burden on the temperature rise of the discharged gas, enables stable # during soot production, increases the soot synthesis rate, and improves the gas of GeO gas. This is to prevent the spread.

なお、スス体製造時のドーパントとして、GeO2に含
む場合、700°C以上に々るとドーパントとしてのG
002制御が不安定になる。丁なわち、スス体製造中に
011ozが酸水素バーナーによりN1ガスと触れた場
合、 GeO2+ H!  →GeO+ H2Oとなシ、この
GeOが沸点710℃であるため蒸発が起りGeoz量
の制御性が低くなる。また加熱ガス吹込みに1シスス体
の温度が7DrJ℃近辺に上昇し次場合、ススは火炎温
度よプ低い所によく着床するため、新たなススの付着量
は削減される。したがって、本発明で加熱ガス吹き込み
によりスス体及びその周辺を加熱する温度については、
上記のような逆効果を生まなり範囲に上限装置くことが
必要である。
In addition, when GeO2 is included as a dopant during the production of soot bodies, when heated to 700°C or higher, G as a dopant is
002 Control becomes unstable. That is, if 011oz comes into contact with N1 gas in an oxyhydrogen burner during soot production, GeO2+ H! →GeO+ Since this GeO has a boiling point of 710° C., evaporation occurs and the controllability of the amount of Geoz becomes poor. Furthermore, if the temperature of the cissus body rises to around 7 DrJ° C. after heating gas is blown in, the amount of new soot deposited is reduced because the soot often settles in areas lower than the flame temperature. Therefore, in the present invention, the temperature at which the soot body and its surroundings are heated by blowing heated gas is as follows:
It is necessary to set an upper limit within the range to prevent the above-mentioned adverse effects.

GeO,Fi一般に光ファイバーのドーパントとして主
力のものであるが、この他のドーパントとして挙げられ
るB503の沸点は1500℃以上であF)、GeO2
の場合の上限温度700℃以下としておけば問題はない
。またP2osもドーパントとして用いるが、これは昇
華し易く560℃で昇華するので、700℃近辺では収
率は非常に悪φ。しかしながら810!に吸着し九P、
O,という形で利用すればよ−ので、pxo=にりiて
はさほど考慮を払う必要がなく、全体として、ドーパン
トの制御はGeO2を主に考えて、700℃以下の温度
で加熱を行なえばよい。
GeO, Fi is generally the main dopant for optical fibers, but other dopants include B503, which has a boiling point of 1500°C or higher (F), GeO2
There is no problem if the upper limit temperature in this case is set to 700°C or less. P2os is also used as a dopant, but it sublimes easily and sublimes at 560°C, so the yield is very poor at around 700°C. However, 810! Adsorbs to 9P,
Since it can be used in the form of Bye.

本発明では第2図に示すように、第1図のマツフル4に
吸気孔7を取υ付け、ここからN2ガス、C02ガスま
たは空気等の気体を加熱器8゛で′加熱し吹き込む。な
お9は吹込み量を調整するためのパルプであp、10t
fN2ガス、CO!ガス、または空気等のボンベである
。なお加熱ガスがN2の場合には、N2ガス吸気孔6と
加熱ガス吹込み孔7を兼用にすることも可能である。
In the present invention, as shown in FIG. 2, an intake hole 7 is attached to the muffler 4 shown in FIG. Note that 9 is pulp for adjusting the amount of blowing, p, 10t.
fN2 gas, CO! It is a cylinder of gas, air, etc. Note that when the heating gas is N2, the N2 gas intake hole 6 and the heating gas blowing hole 7 can also be used.

本発明では、マツフル4内は加熱ガス吹き込みのために
全体が昇温されており、このような状態の中では酸水素
バーナーは原料ガス(840t4、G60j4 、BB
r3 、POCl2婢)の加水分解に必要なH。
In the present invention, the temperature inside Matsufuru 4 is raised as a whole due to the injection of heated gas, and in such a state, the oxyhydrogen burner burns the raw material gas (840t4, G60j4, BB
r3, H required for the hydrolysis of POCl2.

お工び02のガス量の選定に重点を置くことができる。Emphasis can be placed on selecting the amount of gas for work 02.

一方昇温不足に対しては吹き込みガスの温度を調整す、
ることによりバランスが保たれる。
On the other hand, if the temperature rise is insufficient, adjust the temperature of the blown gas.
This maintains balance.

いいかえれば、制御の安定化が図れると共に、バーナー
のN2および03に対する原料ガス量の比會増大させる
ことによりスス体製造効率を上げることができる。
In other words, the control can be stabilized, and the soot body production efficiency can be increased by increasing the ratio of the raw material gas amount to N2 and 03 of the burner.

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

添行の図面はvAD法およびその装置’を説明するため
の概略図で69、第1図が従来法、第2図が本発明方法
に関するものである。 代理人  内 1)   明 代理人 萩 原 亮 −
The accompanying drawings are schematic diagrams 69 for explaining the vAD method and its apparatus, with FIG. 1 relating to the conventional method and FIG. 2 relating to the method of the present invention. Agents 1) Akira’s agent Ryo Hagiwara −

Claims (1)

【特許請求の範囲】 1、  vApgにより党ファイバーの母材となるスス
体を製造する際に、少なくとも酸水素バーナーの炎とス
ス体の一部を包含する容器内に、加熱ガスを吹き込むこ
とを特徴とする、光フアイバー母材の製造方法。 2 酸水素バーナ−、Msガス吸気孔、加熱ガス吸気孔
および排気孔を備え、出発材を1回転しながら上方に引
き上げるような形でその空間内に保持してなる容器であ
ることt+%微とするWAD法における光フアイバー母
材の製造装置。
[Scope of Claims] 1. When producing a soot body to be used as a base material for party fibers using vApg, heating gas is blown into a container containing at least the flame of an oxyhydrogen burner and a part of the soot body. Features: A manufacturing method for optical fiber base material. 2 The container is equipped with an oxyhydrogen burner, Ms gas intake hole, heating gas intake hole, and exhaust hole, and holds the starting material in the space in such a way that it is pulled upward while rotating once. This is an optical fiber base material manufacturing device using the WAD method.
JP14393781A 1981-09-14 1981-09-14 Method and apparatus for manufacturing base material for optical fiber by vad method Pending JPS5845132A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14393781A JPS5845132A (en) 1981-09-14 1981-09-14 Method and apparatus for manufacturing base material for optical fiber by vad method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14393781A JPS5845132A (en) 1981-09-14 1981-09-14 Method and apparatus for manufacturing base material for optical fiber by vad method

Publications (1)

Publication Number Publication Date
JPS5845132A true JPS5845132A (en) 1983-03-16

Family

ID=15350530

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14393781A Pending JPS5845132A (en) 1981-09-14 1981-09-14 Method and apparatus for manufacturing base material for optical fiber by vad method

Country Status (1)

Country Link
JP (1) JPS5845132A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60210540A (en) * 1984-04-04 1985-10-23 Sumitomo Electric Ind Ltd Production of base material for optical fiber
JPS61286241A (en) * 1985-06-12 1986-12-16 Tatsuta Electric Wire & Cable Co Ltd Preparation of parent material for optical fiber
JPS63318043A (en) * 1987-06-19 1988-12-26 Mitsubishi Electric Corp Color drift adjusting method and adjusting device for color cathode-ray tube

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60210540A (en) * 1984-04-04 1985-10-23 Sumitomo Electric Ind Ltd Production of base material for optical fiber
JPS61286241A (en) * 1985-06-12 1986-12-16 Tatsuta Electric Wire & Cable Co Ltd Preparation of parent material for optical fiber
JPS63318043A (en) * 1987-06-19 1988-12-26 Mitsubishi Electric Corp Color drift adjusting method and adjusting device for color cathode-ray tube

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