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JPH0737336B2 - Optical transmitter - Google Patents
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JPH0737336B2 - Optical transmitter - Google Patents

Optical transmitter

Info

Publication number
JPH0737336B2
JPH0737336B2 JP61114358A JP11435886A JPH0737336B2 JP H0737336 B2 JPH0737336 B2 JP H0737336B2 JP 61114358 A JP61114358 A JP 61114358A JP 11435886 A JP11435886 A JP 11435886A JP H0737336 B2 JPH0737336 B2 JP H0737336B2
Authority
JP
Japan
Prior art keywords
core
optical transmission
sodium
hydrogen
ppb
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 - Fee Related
Application number
JP61114358A
Other languages
Japanese (ja)
Other versions
JPS62270441A (en
Inventor
顕 飯野
真雄 西村
勝彦 大久保
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.)
Furukawa Electric Co Ltd
Original Assignee
Furukawa Electric 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 Furukawa Electric Co Ltd filed Critical Furukawa Electric Co Ltd
Priority to JP61114358A priority Critical patent/JPH0737336B2/en
Publication of JPS62270441A publication Critical patent/JPS62270441A/en
Publication of JPH0737336B2 publication Critical patent/JPH0737336B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C13/00Fibre or filament compositions
    • C03C13/04Fibre optics, e.g. core and clad fibre compositions
    • C03C13/045Silica-containing oxide glass compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Glass Compositions (AREA)
  • Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)

Description

【発明の詳細な説明】 〔技術分野〕 本発明は石英ガラスを主成分とする光伝送体に関するも
のである。
TECHNICAL FIELD The present invention relates to an optical transmission body containing silica glass as a main component.

〔従来技術〕[Prior art]

今日光伝送体は公衆通信のみならず、種々の分野で利用
され、応用されているが、この応用分野が拡がるにつれ
て、光伝送体への要求特性も厳しくなってきている。例
えば、耐水素性も厳しくなってきている特性の一つで、
これら特性を改善するため、例えばSiO2-GeO2系の光伝
送体のコア内へのリンの添加量を零にする試み等が成さ
れている。しかしながら耐水素性が改善されるメカニズ
ムが充分解明されず、製造上の制御ポイントは何なのか
解明できないまま今日に至っている。
Today, optical transmitters are used and applied not only in public communication but also in various fields. As the field of application expands, the required characteristics of the optical transmitters are becoming stricter. For example, one of the characteristics that hydrogen resistance is becoming severe,
In order to improve these characteristics, for example, attempts have been made to reduce the amount of phosphorus added to the core of a SiO 2 -GeO 2 -based optical transmission medium to zero. However, the mechanism by which the hydrogen resistance is improved has not been fully elucidated, and the control points in manufacturing have not been elucidated to this day.

〔発明の目的〕[Object of the Invention]

前記問題に鑑み、本発明の目的は光伝送体の耐水素性を
改善する方法を明らかにし、もって耐水素性に優れた光
伝送体を提供することにある。
In view of the above problems, an object of the present invention is to clarify a method for improving the hydrogen resistance of an optical transmission medium, and to provide an optical transmission medium excellent in hydrogen resistance.

〔発明の構成〕[Structure of Invention]

前記目的を達成すべく本発明は、石英ガラスを主成分と
する光伝送体において、該光伝送体の光伝播部が含有す
るアルカリ元素とアルカリ土類元素の重量濃度の和が5p
pb以下であることを特徴とするものである。
In order to achieve the above-mentioned object, the present invention provides an optical transmission body containing silica glass as a main component, wherein the sum of the weight concentrations of alkali elements and alkaline earth elements contained in the light propagating portion of the optical transmission body is 5 p.
It is characterized by being less than or equal to pb.

〔発明の実施例〕Example of Invention

以下に本発明の実施例を図を参照して詳細に説明する。
本発明者は光伝送体の耐水素性の改善を図るべく以下の
実験を行った。まずVAD法、すなわち加炎加水分解法に
よりGI型の屈折率分布を有するコアロッド(組成はSiO2
-GeO2、Δ=1%)を作製し、これを3等分した後、
この中の1本にOVD法等で合成した合成石英管をジャケ
ットしクラッド部を形成した。このときの両者の外径比
はコア:クラッド=50:125であった。これを線引し、か
つ同時にシリコーン樹脂を被覆せしめて第2図に示すよ
うなコア径50μm、クラッド径125μm、被覆径380μm
の光伝送体1を得た。ここで符号2はコア、符号3は前
述の如く合成石英管により構成したクラッド、そして符
号4は被覆を示す。
Embodiments of the present invention will be described in detail below with reference to the drawings.
The present inventor conducted the following experiment in order to improve the hydrogen resistance of the optical transmission medium. First, a core rod having a GI type refractive index distribution (composition is SiO 2) by the VAD method, that is, the flame hydrolysis method.
-GeO 2 , Δ = 1%) was prepared and divided into three,
One of them was jacketed with a synthetic quartz tube synthesized by the OVD method or the like to form a clad portion. At this time, the outer diameter ratio of the two was core: clad = 50: 125. By drawing this and coating with silicone resin at the same time, the core diameter is 50 μm, the cladding diameter is 125 μm, and the coating diameter is 380 μm as shown in FIG.
The optical transmission body 1 of was obtained. Here, reference numeral 2 is a core, reference numeral 3 is a clad constituted by a synthetic quartz tube as described above, and reference numeral 4 is a coating.

前記光伝送体1のコア2を二次イオン質量分析により分
析したところ、不純物はほとんど見出せなかった。この
分析方法の検出下限値は約1ppbであるから、もし不純物
が存在していてもそれ以下であると推定できる。
When the core 2 of the light transmitter 1 was analyzed by secondary ion mass spectrometry, almost no impurities were found. Since the lower limit of detection of this analysis method is about 1 ppb, it can be presumed that it is less than that, even if impurities are present.

次に残りの2本のコアロッドの中に1本に0.03%の塩化
ナトリウム水溶液を塗布し、前記と同一種類の合成石英
管を同一の方法でジャケットし、さらにこれを線引き
し、かつ被覆を施し第2図のような光伝送体1を得た。
これを前記同様にコア2の部分の組成を二次イオン質量
分析で調べたところ、ナトリウムが0.07ppm見出され
た。
Next, 0.03% sodium chloride aqueous solution is applied to one of the remaining two core rods, a synthetic quartz tube of the same type as the above is jacketed by the same method, and then this is drawn and coated. The optical transmission body 1 as shown in FIG. 2 was obtained.
When the composition of the core 2 portion was examined by secondary ion mass spectrometry in the same manner as described above, 0.07 ppm of sodium was found.

同様に3本目のコアロッドにより高濃度である0.1%の
塩化ナトリウム水溶液を塗布し、前記2本と同一の種類
の合成石英管を同様の方法でジャケットし、同様の方法
で第2図に示すような光伝送体1を得た。この光伝送体
1のコア2の部分を二次イオン質量分析で分析したらナ
トリウムが0.2ppm見出された。
Similarly, a high concentration of 0.1% sodium chloride aqueous solution is applied to the third core rod, a synthetic quartz tube of the same type as the above two is jacketed in the same manner, and the same method is used as shown in FIG. The optical transmission body 1 was obtained. When the core 2 portion of this optical transmitter 1 was analyzed by secondary ion mass spectrometry, 0.2 ppm of sodium was found.

以上3種のGI型光伝送体1を200℃の水素雰囲気下に4
時間曝した。この結果各々が波長1.41〜1.42μmのとこ
ろでGeOH基に起因すると推定される吸収ピーク値を示し
た。この結果をまとめたものを第1図に示す。第1図が
示すようにコア2中のナトリウムの量が増える程前記吸
収ピーク値は大きくなった。
The above three types of GI type optical transmitters 1 were placed in a hydrogen atmosphere at 200 ° C.
Exposed for hours. As a result, each showed an absorption peak value estimated to be caused by a GeOH group at a wavelength of 1.41 to 1.42 μm. A summary of these results is shown in FIG. As shown in FIG. 1, the absorption peak value increased as the amount of sodium in the core 2 increased.

さてこの結果により本発明者は以下のように推定した。
すなわちコア2とクラッド3の界面に存在するナトリウ
ムは、SiO2-GeO2ガラス構造を乱し、、特にゲルマニウ
ムに関連した欠陥の前駆体を発生せしめていて、この状
態で200℃の水素雰囲気に曝されると、前記欠陥の前駆
体と水素とが反応して水素により伝送ロス増加の問題と
なるGeOH基が発生する、と推論した。
Based on this result, the present inventor estimated as follows.
That is, sodium existing at the interface between the core 2 and the clad 3 disturbs the SiO 2 —GeO 2 glass structure, and particularly generates a precursor of defects related to germanium, and in this state, it is exposed to a hydrogen atmosphere at 200 ° C. It was inferred that upon exposure, the precursor of the defect reacts with hydrogen to generate a GeOH group, which causes a problem of increased transmission loss due to hydrogen.

次に第1図が示すようにナトリウムが1ppb以下でも約2d
B/kmのロス増加が見られるが、この原因はSiO2-GeO2
ラスがナトリウムによらず、もともと持っている固有の
欠陥に起因すると推定した。そこでナトリウム濃度が10
ppb以下での挙動を再度調査した結果、第1図の矢印(5
ppbを示す)が示すように5ppb以下ではロス増加は約2dB
/kmとほぼ一定であって、これ以上になるとコア内のナ
トリウム重量濃度に比例してロス増加が進むことがわか
った。
Next, as shown in Fig. 1, it is about 2d even if sodium is less than 1ppb.
The increase of B / km loss is observed, and it is presumed that the cause is the intrinsic defect of SiO 2 -GeO 2 glass, not the one of sodium. So the sodium concentration is 10
As a result of investigating the behavior below ppb again, the arrow (5
ppb), the loss increase is about 2 dB below 5 ppb.
It was found to be almost constant as / km, and beyond this, it was found that the loss increases in proportion to the sodium weight concentration in the core.

以上の結果から本発明者は、コア2内及びコア2に近接
するクラッド3の一部、すなわち光伝播部のナトリウム
による汚染を5ppb以下にすれば水素によるロス増加を防
止できる、という重要な知見を得るに至った。
From the above results, the present inventor has an important finding that the loss increase due to hydrogen can be prevented by reducing the sodium contamination in the part of the clad 3 inside the core 2 and in the vicinity of the core 2, that is, the light propagating portion to 5 ppb or less. Came to get.

ところでナトリウムのコアへの含有濃度を5ppb以下にす
る方法であるが、例えば、VAD法にて作製したコアロッ
ドを予め5%のフッ化水素水溶液に5分間程度浸し、こ
れを高純度(イオン交換+蒸溜を行った)蒸留水で充分
洗浄した後、直ちに前記合成石英管、すなわちVAD法、O
VD法あるいはプラズマ法等で作製した合成石英管をジャ
ケットする方法、あるいは前述のように洗浄したコアロ
ッド外周に、直ちにOVD法にてクラッド部等を堆積せし
め、該堆積部分を脱水.透明化する方法等がある。尚こ
れらの操作はすべてクリーン度が100〜1000程度の清浄
な雰囲気下が行う必要がある。その理由は、空気中に放
置するだけでコアロッド表面あるいはクラッド表面が空
気中のナトリウムやカリウム等により汚染されるからで
ある。
By the way, it is a method of setting the content concentration of sodium in the core to 5 ppb or less. For example, a core rod prepared by the VAD method is immersed in a 5% hydrogen fluoride aqueous solution for about 5 minutes in advance, and this is highly purified (ion exchange + After thorough washing with distilled water, the synthetic quartz tube, that is, the VAD method, O
The synthetic quartz tube produced by the VD method or the plasma method was jacketed, or the clad portion was immediately deposited on the outer periphery of the core rod cleaned as described above by the OVD method, and the deposited portion was dehydrated. There is a method to make it transparent. All of these operations must be performed in a clean atmosphere with a cleanliness of 100 to 1000. The reason is that the core rod surface or the clad surface is contaminated by sodium, potassium, etc. in the air simply by leaving it in the air.

尚これまではナトリウムについてのみ述べたがその性質
からしてリチウム、カリウム、ルビジウム、セシウム、
カルシウムあるいはマグネシウム等のアルカリ元素、ア
ルカリ土類元素についても同様なことが言え、その総和
を5ppb以下にする必要がある。またコア2の組成につい
ても前記SiO2-GeO2系ガラス以外にSiO2ガラスやSiO2-F
系ガラスについても同様である。
So far, only sodium has been described, but due to its properties, lithium, potassium, rubidium, cesium,
The same can be said for alkaline elements such as calcium or magnesium, and alkaline earth elements, and the total sum must be 5 ppb or less. Also, regarding the composition of the core 2, in addition to the SiO 2 -GeO 2 system glass, SiO 2 glass or SiO 2 -F
The same applies to the system glass.

以上に述べた如く、コア部分及び該コアに隣接するクラ
ッドの一部、すなわち光伝播部のアルカリ元素+アルカ
リ土類元素の濃度和を5ppb以下にすることにより光伝送
体の耐水素性を著しく向上させることが可能となった。
また本発明の光伝送体の耐放射線性について調査したと
ころ、やはり特性の向上が見られた。その理由は、耐水
素性と同様にガラス構造を乱すアルカリ元素、アルカリ
土類元素を減少せしめた結果であると推定される。
As described above, the hydrogen resistance of the optical transmission element is remarkably improved by setting the sum of the concentrations of the alkali element and the alkaline earth element in the light propagating portion, that is, the core portion and a part of the clad adjacent to the core, to 5 ppb or less. It became possible to do.
In addition, when the radiation resistance of the optical transmission article of the present invention was investigated, it was also found that the characteristics were improved. The reason is presumed to be the result of reducing the alkali elements and alkaline earth elements that disturb the glass structure as well as the hydrogen resistance.

〔発明の効果〕〔The invention's effect〕

前述の如く本発明によれば、光伝送体の耐水素ロス増加
を最小限に押さえることができる。
As described above, according to the present invention, it is possible to minimize the increase in hydrogen loss resistance of the optical transmission body.

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

第1図は本発明に係わる実験結果を示すグラフ、第2図
は光伝送体の横断面図である。 1〜光伝送体、2〜コア、3〜クラッド
FIG. 1 is a graph showing the experimental results according to the present invention, and FIG. 2 is a transverse sectional view of an optical transmission body. 1-optical transmission body, 2-core, 3-clad

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】石英ガラスを主成分とする光伝送体におい
て、該光伝送体の光伝播部が含有するアルカリ元素とア
ルカリ土類元素の重量濃度の和が5ppb以下であることを
特徴とする光伝送体。
1. A light transmission body containing quartz glass as a main component, wherein the sum of the weight concentrations of alkali elements and alkaline earth elements contained in the light propagation section of the light transmission body is 5 ppb or less. Optical transmitter.
【請求項2】前記光伝送体の光伝播部はSiO2-GeO2から
なることを特徴とする特許請求の範囲第1項記載の光伝
送体。
2. The optical transmission medium according to claim 1, wherein the light propagation portion of the optical transmission medium is made of SiO 2 --GeO 2 .
JP61114358A 1986-05-19 1986-05-19 Optical transmitter Expired - Fee Related JPH0737336B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61114358A JPH0737336B2 (en) 1986-05-19 1986-05-19 Optical transmitter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61114358A JPH0737336B2 (en) 1986-05-19 1986-05-19 Optical transmitter

Publications (2)

Publication Number Publication Date
JPS62270441A JPS62270441A (en) 1987-11-24
JPH0737336B2 true JPH0737336B2 (en) 1995-04-26

Family

ID=14635724

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61114358A Expired - Fee Related JPH0737336B2 (en) 1986-05-19 1986-05-19 Optical transmitter

Country Status (1)

Country Link
JP (1) JPH0737336B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01167258A (en) * 1987-12-23 1989-06-30 Shinetsu Sekiei Kk Element assembly of laser optical system
JPH035338A (en) * 1989-05-30 1991-01-11 Shinetsu Sekiei Kk Optical member for laser light
JP5974488B2 (en) * 2011-04-15 2016-08-23 住友電気工業株式会社 Optical fiber and optical fiber preform

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
OPTICAL FIBER COMMUNICATION CONFERENCE=1986 *

Also Published As

Publication number Publication date
JPS62270441A (en) 1987-11-24

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