JPH10120429A - Burner for producing fine glass particle - Google Patents

Burner for producing fine glass particle

Info

Publication number
JPH10120429A
JPH10120429A JP8274342A JP27434296A JPH10120429A JP H10120429 A JPH10120429 A JP H10120429A JP 8274342 A JP8274342 A JP 8274342A JP 27434296 A JP27434296 A JP 27434296A JP H10120429 A JPH10120429 A JP H10120429A
Authority
JP
Japan
Prior art keywords
gas
raw material
glass
flame
fine glass
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
Application number
JP8274342A
Other languages
Japanese (ja)
Other versions
JP3169561B2 (en
Inventor
Kazuhisa Hatayama
和久 畑山
Tadakatsu Shimada
忠克 島田
Hideo Hirasawa
秀夫 平沢
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.)
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co 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 Shin Etsu Chemical Co Ltd filed Critical Shin Etsu Chemical Co Ltd
Priority to JP27434296A priority Critical patent/JP3169561B2/en
Publication of JPH10120429A publication Critical patent/JPH10120429A/en
Application granted granted Critical
Publication of JP3169561B2 publication Critical patent/JP3169561B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B19/00Other methods of shaping glass
    • C03B19/14Other methods of shaping glass by gas- or vapour- phase reaction processes
    • C03B19/1415Reactant delivery systems
    • C03B19/1423Reactant deposition burners
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2207/00Glass deposition burners
    • C03B2207/04Multi-nested ports
    • C03B2207/06Concentric circular ports
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2207/00Glass deposition burners
    • C03B2207/20Specific substances in specified ports, e.g. all gas flows specified
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2207/00Glass deposition burners
    • C03B2207/20Specific substances in specified ports, e.g. all gas flows specified
    • C03B2207/22Inert gas details
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2207/00Glass deposition burners
    • C03B2207/36Fuel or oxidant details, e.g. flow rate, flow rate ratio, fuel additives

Abstract

PROBLEM TO BE SOLVED: To efficiently produce and deposit fine glass particles by making a specific O2 -containing gas flow to the outermost layer of a multitubular burner for producing the fine glass particles by hydrolytic reaction of a glass raw material gas in a flame therein. SOLUTION: This multitubular burner for producing fine glass particles is capable of making an O2 -containing gas which is an inert gas such as preferably N2 gas, He or Ar gas containing O2 at 15-25vol.% concentration or air flow to the outermost layer of the multitubular burner. The feed rate of the O2 -containing gas is preferably 3-60vol.% based on the glass raw material (e.g. SiCl4 gas) and the flow velocity of the O2 -containing gas is preferably 0.1-3 times that of the glass raw material gas. As a result, the diffusion and converging of a flame can be prevented and controlled and the temperature distribution in the flame in regions for producing and depositing the fine glass particles can be optimized. Thereby, the fine glass particles can efficiently be produced and deposited.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は光ファイバ用ガラス
母材等の製造に使用されるガラス微粒子生成用バーナー
に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a burner for producing glass fine particles used for producing a glass preform for optical fibers and the like.

【0002】[0002]

【従来の技術】ガラス微粒子を生成する方法として、ガ
ラス原料ガスを火炎中で加水分解反応させる方法があ
る。光ファイバ用ガラス母材の製造においては、ガラス
原料ガスとして四塩化ケイ素(SiCl4) などのケイ素化合
物に、屈折率を上げるためのドーパント原料の四塩化ゲ
ルマニウム(GeCl4) などがあり、これらを水素ガス
(H2)、メタンガス(CH4) などの可燃性ガスと、酸素ガス
(O2)などの助燃性ガスの混合炎中に供給して加水分解し
てガラス微粒子を生成する。これを耐熱性のターゲット
やガラスロッドに堆積させて堆積体とする場合もある。
2. Description of the Related Art As a method for producing glass fine particles, there is a method in which a glass raw material gas is subjected to a hydrolysis reaction in a flame. In the production of glass preforms for optical fibers, as a glass raw material gas, a silicon compound such as silicon tetrachloride (SiCl 4 ) has a dopant raw material for increasing the refractive index, such as germanium tetrachloride (GeCl 4 ). Hydrogen gas
(H 2 ), flammable gas such as methane gas (CH 4 ), and oxygen gas
It is supplied into a mixed flame of an auxiliary combustion gas such as (O 2 ) and hydrolyzed to generate glass fine particles. This may be deposited on a heat-resistant target or glass rod to form a deposit.

【0003】[0003]

【発明が解決しようとする課題】しかし、ガラス原料ガ
ス、可燃性ガス及び助燃性ガスの供給量は、ガラス微粒
子の生成の場合と、ガラス微粒子を被付着体に堆積させ
る場合とでは最適供給量は一般的に差があり、前者の場
合、通常は生成、堆積における最適原料供給量の中間の
原料供給量で生成、堆積せざるをえない。例えば、ガラ
ス微粒子の生成の場合は、最適ガス供給量は、容量比で
ガラス原料ガス1に対して、可燃性ガス2〜40及び助燃
性ガス1〜20であるが、一方ガラス微粒子を被付着体に
堆積させる場合は、最適ガス供給量は、容量比でガラス
原料ガス1に対して、可燃性ガス2〜40及び助燃性ガス
1.5 〜15である。また、従来のガラス微粒子生成用バー
ナーは、形状、供給する各原料ガスの種類や量の如何に
関わらず、ガラス微粒子を生成する最適ガス供給量で
は、多重管バーナー最外層のガス流速がガラス原料ガス
流速との差が大きいため、火炎が拡散ないしは収束して
しまう。このため、ガラス微粒子を被付着体に堆積する
場合、ガラス微粒子の堆積効率が悪くなり、また堆積後
の多孔質ガラス体の密度も低下する。
However, the supply amounts of the glass raw material gas, the flammable gas, and the auxiliary combustion gas are optimal supply amounts in the case of generating glass particles and in the case of depositing glass particles on an adherend. Generally, there is a difference. In the former case, it is usually necessary to generate and deposit a raw material supply amount that is intermediate between the optimum raw material supply amounts in generation and deposition. For example, in the case of producing glass particles, the optimum gas supply amount is a combustible gas of 2 to 40 and a combustible gas of 1 to 20 with respect to the glass raw material gas 1 by volume ratio. In the case of depositing on the body, the optimum gas supply amount is the ratio of the flammable gas 2 to 40 and the auxiliary gas
1.5 to 15. In addition, conventional burners for producing glass fine particles require that the gas flow rate of the outermost layer of the multi-tube burner be controlled by the optimal gas supply amount for generating glass fine particles, regardless of the shape and the type and amount of each raw material gas supplied. Since the difference from the gas flow velocity is large, the flame spreads or converges. For this reason, when glass particles are deposited on the adherend, the deposition efficiency of the glass particles is deteriorated, and the density of the porous glass body after the deposition is reduced.

【0004】[0004]

【課題を解決するための手段】本発明は、上記の問題点
に鑑みなされたもので、ガラス微粒子の生成及び付着領
域での火炎中の温度分布を最適化させ、効率良くガラス
微粒子の生成、堆積をすることができる。即ち本発明
は、火炎中でガラス原料ガスの加水分解反応によりガラ
ス微粒子を生成する多重管バーナーにおいて、その最外
層に酸素濃度が15〜25容量%の酸素含有ガスを流すこと
を特徴とするものである。
SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned problems, and has been made in consideration of the above-mentioned problems. Deposits can be made. That is, the present invention is characterized in that an oxygen-containing gas having an oxygen concentration of 15 to 25% by volume flows through the outermost layer of a multi-tube burner that produces glass fine particles by a hydrolysis reaction of a glass raw material gas in a flame. It is.

【0005】[0005]

【発明の実施の形態】本発明は、多重管バーナーの最外
層に酸素含有ガスを流すことにより、火炎の拡散、収束
を防ぎ、これを自由に制御することができ、またその供
給量を調節することで火炎全体の拡散を制御し、ガラス
微粒子の生成領域及び堆積領域での火炎中の温度分布を
最適化させることができ、効率よくガラス微粒子の生
成、堆積が行われるのである。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention prevents the diffusion and convergence of a flame by flowing an oxygen-containing gas to the outermost layer of a multi-tube burner, and can control the flame freely, and regulates the supply amount. By doing so, it is possible to control the diffusion of the entire flame, optimize the temperature distribution in the flame in the generation region and the deposition region of the glass fine particles, and efficiently generate and deposit the glass fine particles.

【0006】酸素含有ガスの酸素濃度は15容量%未満で
は、火炎の温度が低下し、堆積後の多孔質ガラス体の密
度が低くなり、25容量%を超えると火炎温度が最適なガ
ラス微粒子生成領域から逸脱し、ガラス微粒子の生成及
び堆積効率が低下するので、15〜25容量%の範囲とする
ことが必要である。酸素含有ガスとしては、窒素ガスや
Heガス、Arガス等の不活性ガスに酸素を含有させたもの
や空気などが好ましい。酸素含有ガスの供給量は、火炎
中のガラス微粒子の生成領域の温度分布に悪影響を及ぼ
さず、ガラス微粒子の堆積に最適な温度領域をより大き
く確保する理由から、ガラス原料ガスの3〜60容量%と
するのが好ましい。また、酸素含有ガスの流速をガラス
原料ガスの流速の0.1 〜3倍とすることにより、火炎の
拡散や収束を防止することができる。
[0006] If the oxygen concentration of the oxygen-containing gas is less than 15% by volume, the temperature of the flame is lowered, and the density of the porous glass body after deposition is reduced. Since it deviates from the range and the production efficiency and deposition efficiency of the glass fine particles decrease, it is necessary to set the range of 15 to 25% by volume. Examples of oxygen-containing gas include nitrogen gas and
An inert gas such as He gas or Ar gas containing oxygen or air is preferable. The supply amount of the oxygen-containing gas does not adversely affect the temperature distribution in the region in which the glass fine particles are generated in the flame, and a range of 3 to 60 volumes of the glass raw material gas is used because the temperature range optimal for the deposition of the glass fine particles is more secured. % Is preferable. Further, by setting the flow rate of the oxygen-containing gas to be 0.1 to 3 times the flow rate of the glass raw material gas, it is possible to prevent the diffusion and convergence of the flame.

【0007】本発明では、ガラス微粒子を被付着体に堆
積させる場合でも、ガラス原料ガス、可燃性ガス、助燃
性ガスの供給量はガラス微粒子生成効率が最適のものと
すれば良く、これは公知の条件で行えばよく、例えば容
量比でガラス原料ガス1に対して可燃性ガス2〜40、助
燃性ガス1〜20の比率とすればよい。
In the present invention, even when glass particles are deposited on the adherend, the supply amounts of the glass raw material gas, the flammable gas, and the auxiliary gas may be determined so that the glass particle generation efficiency is optimal. For example, the ratio of the combustible gas 2 to 40 and the combustible gas 1 to 20 with respect to the glass raw material gas 1 may be set as the volume ratio.

【0008】多重管バーナーは公知のもので良く、例え
ば中心管よりガラス原料ガス、助燃性ガス、可燃性ガ
ス、シールガス及び最外層に酸素含有ガスのノズルをこ
の順で設けた5重管が例示されるが、本願発明では、5
重管に限定されるものではなく、5重管より多くても少
なくとも良く、要は最外層に酸素含有ガスのノズルが設
けられていれば良い。
The multi-tube burner may be a known one. For example, a quintuple tube having nozzles for a glass raw material gas, a combustible gas, a flammable gas, a seal gas, and an oxygen-containing gas provided in the outermost layer in this order from the center tube is used. As an example, in the present invention, 5
The present invention is not limited to a heavy pipe, and may be at least more than a five-ply pipe. In short, it is sufficient that an oxygen-containing gas nozzle is provided in the outermost layer.

【0009】[0009]

【実施例】【Example】

実施例 5重管バーナーの中心ノズルより順に、四塩化ケイ素ガ
ス10SLM (標準状態でのガス供給速度、リットル/分、
以下同じ)、水素ガス150SLM、酸素ガス100SLM、アルゴ
ンガス10SLM を各ノズルに供給し、最外層のノズルには
空気5SLM を供給し、この空気により火炎の拡散を防ぎ
ながら、寸法50mm×50mm×3mm厚さのガラス板に、この
火炎をガラス板の表面から垂直に30cm離して、ガラス微
粒子を7mmの厚さに堆積させたところ、堆積効率は全ガ
ラス微粒子量の53%となり、堆積密度は0.6g/cm3であっ
た。
Example 5 In order from the center nozzle of a quintuple tube burner, silicon tetrachloride gas 10SLM (gas supply rate under standard conditions, liter / min,
The same applies to the following), 150 SLM of hydrogen gas, 100 SLM of oxygen gas, and 10 SLM of argon gas are supplied to each nozzle, and 5 SLM of air is supplied to the outermost nozzle. When this flame was vertically separated from the surface of the glass plate by 30 cm on a glass plate having a thickness of 7 mm and the glass particles were deposited to a thickness of 7 mm, the deposition efficiency was 53% of the total glass particle amount, and the deposition density was 0.6%. g / cm 3 .

【0010】比較例 5重管バーナーの最外層のノズルに空気を供給しなかっ
た点以外は実施例と同じ条件でガラス微粒子を堆積した
ところ、堆積効率は全ガラス微粒子量の47%で、堆積密
度は0.45g/cm3 であった。
Comparative Example When glass fine particles were deposited under the same conditions as in the example except that air was not supplied to the outermost nozzle of the five-tube burner, the deposition efficiency was 47% of the total glass fine particle amount. The density was 0.45 g / cm 3 .

【0011】[0011]

【発明の効果】本発明によれば、効率よくガラス微粒子
を生成、堆積することができる。
According to the present invention, glass particles can be efficiently generated and deposited.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】火炎中でガラス原料ガスの加水分解反応に
よりガラス微粒子を生成する多重管バーナーにおいて、
その最外層に酸素濃度が15〜25容量%の酸素含有ガスを
流すことを特徴とするガラス微粒子生成用バーナー。
1. A multi-tube burner for producing glass fine particles by a hydrolysis reaction of a glass raw material gas in a flame,
A burner for producing glass fine particles, characterized in that an oxygen-containing gas having an oxygen concentration of 15 to 25% by volume is passed through the outermost layer.
JP27434296A 1996-10-17 1996-10-17 Method for producing glass particle deposit Expired - Fee Related JP3169561B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27434296A JP3169561B2 (en) 1996-10-17 1996-10-17 Method for producing glass particle deposit

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27434296A JP3169561B2 (en) 1996-10-17 1996-10-17 Method for producing glass particle deposit

Publications (2)

Publication Number Publication Date
JPH10120429A true JPH10120429A (en) 1998-05-12
JP3169561B2 JP3169561B2 (en) 2001-05-28

Family

ID=17540329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27434296A Expired - Fee Related JP3169561B2 (en) 1996-10-17 1996-10-17 Method for producing glass particle deposit

Country Status (1)

Country Link
JP (1) JP3169561B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003252643A (en) * 2002-03-04 2003-09-10 Fujikura Ltd Production method for optical fiber preform, and oxyhydrogen flame burner

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654243A (en) * 1979-10-12 1981-05-14 Hitachi Ltd Preparation of optical fiber matrix
JPS605036A (en) * 1983-05-31 1985-01-11 アメリカン テレフォン アンド テレグラフ カムパニー Manufacture of single mode light conducting preform
JPS60215515A (en) * 1984-04-10 1985-10-28 Mitsubishi Metal Corp Preparation of synthetic quartz mass and device therefor
JPH01142425U (en) * 1988-03-22 1989-09-29
JPH0290631U (en) * 1988-12-27 1990-07-18
JPH04193730A (en) * 1990-11-26 1992-07-13 Fujikura Ltd Production of base material for optical fiber and hood for oxyhydrogen burner

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654243A (en) * 1979-10-12 1981-05-14 Hitachi Ltd Preparation of optical fiber matrix
JPS605036A (en) * 1983-05-31 1985-01-11 アメリカン テレフォン アンド テレグラフ カムパニー Manufacture of single mode light conducting preform
JPS60215515A (en) * 1984-04-10 1985-10-28 Mitsubishi Metal Corp Preparation of synthetic quartz mass and device therefor
JPH01142425U (en) * 1988-03-22 1989-09-29
JPH0290631U (en) * 1988-12-27 1990-07-18
JPH04193730A (en) * 1990-11-26 1992-07-13 Fujikura Ltd Production of base material for optical fiber and hood for oxyhydrogen burner

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003252643A (en) * 2002-03-04 2003-09-10 Fujikura Ltd Production method for optical fiber preform, and oxyhydrogen flame burner

Also Published As

Publication number Publication date
JP3169561B2 (en) 2001-05-28

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