JPS6024060B2 - Optical fiber core glass for endoscopes - Google Patents

Optical fiber core glass for endoscopes

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Publication number
JPS6024060B2
JPS6024060B2 JP55182443A JP18244380A JPS6024060B2 JP S6024060 B2 JPS6024060 B2 JP S6024060B2 JP 55182443 A JP55182443 A JP 55182443A JP 18244380 A JP18244380 A JP 18244380A JP S6024060 B2 JPS6024060 B2 JP S6024060B2
Authority
JP
Japan
Prior art keywords
optical fiber
core glass
glass
endoscopes
optical fibers
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
Application number
JP55182443A
Other languages
Japanese (ja)
Other versions
JPS57106538A (en
Inventor
勇朋 原田
重男 桑山
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.)
Fujinon Corp
Original Assignee
Fuji Photo Optical 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 Fuji Photo Optical Co Ltd filed Critical Fuji Photo Optical Co Ltd
Priority to JP55182443A priority Critical patent/JPS6024060B2/en
Publication of JPS57106538A publication Critical patent/JPS57106538A/en
Publication of JPS6024060B2 publication Critical patent/JPS6024060B2/en
Expired legal-status Critical Current

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  • Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
  • Glass Compositions (AREA)

Description

【発明の詳細な説明】 本発明は内視鏡用光学繊維の芯ガラスの改良に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in the core glass of optical fibers for endoscopes.

光学繊維東がイメージ・ガイドとして使用される場合に
は、その光学繊維東はその端部が一対一に対応して配列
されている必要がある。
When optical fibers East are used as image guides, the optical fibers East must be arranged in a one-to-one correspondence with their ends.

とりわけイメージ・ガイド用光学繊維東が内視鏡などと
して使用される場合には、上記光学繊維東はその両端に
おいて互いに固着され、その中間部分は可榛性であるこ
とが要求されることが多い。更に上記各光学繊維の着色
はできるだけ少くしかも均一であることが必要である。
各光学繊維の着色が非常に少し、場合であっても各光学
繊維間に着色の不均一が存在すると内視鏡の視野に色む
らを生じ不良となる。本発明は上記各光学繊維の不均一
を少くして内視鏡用光学繊維東の得率を向上させるため
に必要な芯ガラスに関するものである。
Particularly when the image guide optical fiber east is used as an endoscope, it is often required that the optical fiber east be fixed to each other at both ends and that the intermediate portion be flexible. . Further, it is necessary that the coloring of each of the above-mentioned optical fibers be as little as possible and uniform.
Even if each optical fiber is very slightly colored, if there is uneven coloring among the optical fibers, color unevenness will occur in the field of view of the endoscope, resulting in defects. The present invention relates to a core glass necessary for improving the yield of optical fibers for endoscopes by reducing the non-uniformity of each optical fiber.

ところで従来上記のような固着された端部及び可擬性の
ある中間部を有する光学繊維束は次のような方法で製造
されている。例えば2重白金柑禍に内側の白金均禍に屈
折率の比較的高い芯ガラスを、外側の白金柑禍に屈折率
の比較的低い被覆ガラスを夫々入れ、該2重白金柑渦を
適当な温度(例えば約1000午0)に加熱し、白金柑
渦の底部孔から両ガラスを引き芯ガラスに被覆ガラスを
被覆し、得られた光学繊維を一列のループ状に隙間なく
巻きとり、該ループのーケ所を接着剤で固着し、その上
に前回と同様にして一列にループ状に隙間なく巻き、前
に形成したループの固着部において接着剤で固着し、該
操作を繰返して所望の厚さのループ状光学繊維東を得、
該ループ状光学繊維東の固着部のほぼ中央を光学繊維の
長さに対して直角に切断しついで、この二つの切断面を
研磨して可捺性を有するイメージ・ガイド用光学繊維束
が作られる。この方法においては芯ガラスとしてフリン
トガラス〔重量組成;Si02=44.3%、POO=
45.7%、K20=6.3%、Na20=3.1%、
AI203=約0.2%、AS203=0.3%、比重
=3.61、nd=1.6200、Vd=36.3、転
位点=44〆C、屈曲点=482℃、膨脹係数97×1
び(抑/肌℃)〕を用い、被覆ガラスとしてクラウンガ
ラス〔重量組成;Si02=65.6%、Ca○=5.
0%、Mg0=3.8%、K20=1.5%、Na20
=16.1%、N203=2.3%、Ba○=2.3%
、B203=2.2%、松203=0.4%、比重=2
.55、nd=1.5212、Vd=59.ん転位点=
528qo、屈曲点:570℃、膨脹係数98×10‐
7(肌/肌℃)〕が使用されている。前述のように芯ガ
ラスとしてPのの多いフリントガラスが白金柑渦で溶解
されると白金が僅かであるがガラス中にとげてガラスを
着色する。この着色の程度は非常に不規則で、ある時は
大で、ある時は小となる。しかも出釆た光学繊維を1本
1本検査しても殆んど差を発見することができないが光
学繊維東として組み上げたときに色むらとして不合格に
なる。本発明は上記のような欠点を解消するために芯ガ
ラスのPb○をZn0やBa0などに置換してPのによ
る着色の欠点を少くし、Pのの減少による屈折率の低下
を防止し、更にPOOの減少による加工性の悪化を軽減
し、高得率の内視鏡用光学繊維の芯ガラスを提供するも
のである。更に可鏡性を有する光学繊維東を内視鏡など
として用いる場合内視鏡を体内に挿入し体外から観察個
所をX線で照射することがいよいよ行われる。この場合
Pのの含有量の大なる芯ガラスの場合はPb0の含有量
の小なる芯ガラスに比して非常に着色しやすく比較的短
期間に使用不可能となる。本発明のもつ一つの目的は上
記のような欠点を解消するため芯ガラスのPOOをBa
○などに置換してPOOの含有量を少くし、X線照射に
より着色し難い、比較的長期間使用可能な(例えば寿命
が約20%長くなる)内視鏡用光学繊維東の芯ガラスを
提供するものである。又可凝性を有する光学繊維東を内
視鏡などのライト・ガイドとして用いる場合、光源とし
て高輝度キセノンランプが用いられ、このキセノンラン
プからの放射光線を光学繊維東の端面により多く集光さ
せ光学繊維東を通して被写体をできるだけ明るく照明す
る必要がある。最近は光学繊維東の径をできるだけ小に
してしかもできるだけ明るく照明することが要求されて
釆ている。このため光源が更に高輝度となり、受光する
光学繊維東の端面の温度が高温(例えば500〜600
oo)になり、長時間使用中に光学繊維東の端面が変形
」又は失透を生じ明るさが減少する。本発明のもう一つ
の目的は上記のような欠点を解消するため、芯ガラスの
PのをBaoなどに置換してPboの含有量を少くし、
耐熱温度を例えば約100qo高くして、光学繊維東の
端面の変形、失透が少く、長時間使用可能な内視鏡用光
学繊維東の芯ガラスを堤供するものである。Pのの含有
量をゼoにして光学繊維の透過率を改良することに関し
ては既に特開昭53−60240、特開昭54一872
36に開示されているが、Pboの含有量をゼロとし、
Ca○を必須成分とした場合温度に対する粘度の変化が
大となり、加工性が悪くなり、内視鏡用光学繊維のよう
に座が小さくて寸法精度の厳しい光学繊維を作ることは
非常に難しい。本発明は重量比にて下記の組成よりなる
ことを特徴とする内視鏡における光学繊維用芯ガラスに
関するものである。
By the way, optical fiber bundles having fixed end portions and a flexible intermediate portion as described above have conventionally been manufactured by the following method. For example, in a double platinum vortex, a core glass with a relatively high refractive index is placed in the inner platinum vortex, and a covering glass with a relatively low refractive index is placed in the outer platinum vortex. Heating the glass to a temperature (for example, about 1000 pm), pull both glasses through the bottom hole of the platinum vortex, coat the core glass with the coated glass, and wind the obtained optical fiber into a row of loops without gaps. Fix the hole with adhesive, wrap it in a line in a loop shape without any gaps in the same way as before, fix with adhesive at the fixed part of the loop formed before, and repeat this operation until the desired thickness is reached. Obtain a loop-shaped optical fiber,
A flexible optical fiber bundle for an image guide is produced by cutting approximately the center of the fixed portion of the looped optical fiber at a right angle to the length of the optical fiber, and polishing these two cut surfaces. It will be done. In this method, the core glass is flint glass [weight composition: Si02 = 44.3%, POO =
45.7%, K20=6.3%, Na20=3.1%,
AI203=about 0.2%, AS203=0.3%, specific gravity=3.61, nd=1.6200, Vd=36.3, dislocation point=44〆C, bending point=482℃, expansion coefficient 97× 1
Crown glass [weight composition: Si02 = 65.6%, Ca○ = 5.0%] was used as the coating glass.
0%, Mg0=3.8%, K20=1.5%, Na20
=16.1%, N203=2.3%, Ba○=2.3%
, B203=2.2%, Pine 203=0.4%, Specific gravity=2
.. 55, nd=1.5212, Vd=59. Dislocation point=
528qo, bending point: 570℃, expansion coefficient 98×10-
7 (skin/skin temperature)] is used. As mentioned above, when a flint glass containing a large amount of P is melted in a platinum vortex as a core glass, a small amount of platinum is splintered into the glass and colors the glass. The degree of this coloring is very irregular, sometimes being large and sometimes being small. Moreover, even if the optical fibers are inspected one by one, it is almost impossible to find any differences, but when assembled as optical fibers, the fibers are rejected due to uneven coloring. In order to eliminate the above-mentioned drawbacks, the present invention replaces Pb○ in the core glass with Zn0, Ba0, etc. to reduce the drawback of coloring due to P, and prevent a decrease in refractive index due to a decrease in P. Further, the present invention provides a core glass for optical fibers for endoscopes that reduces the deterioration of workability due to a decrease in POO and has a high yield. Furthermore, when the optical fiber Higashi having specularity is used as an endoscope or the like, the endoscope is inserted into the body and the observation site is irradiated with X-rays from outside the body. In this case, a core glass with a high P content is much more likely to be colored than a core glass with a low Pb0 content and becomes unusable in a relatively short period of time. One purpose of the present invention is to solve the above-mentioned drawbacks by converting the POO of the core glass into Ba.
○ etc. to reduce the content of POO, and create a core glass for endoscope optical fibers that is not easily colored by X-ray irradiation and can be used for a relatively long period of time (for example, the lifespan is about 20% longer). This is what we provide. Furthermore, when optical fibers with condensable properties are used as light guides in endoscopes, etc., a high-intensity xenon lamp is used as the light source, and more of the radiation from the xenon lamp is focused on the end face of the optical fibers. It is necessary to illuminate the subject as brightly as possible through the optical fiber east. Recently, there has been a need to make the diameter of the optical fiber as small as possible and to provide as much illumination as possible. As a result, the light source becomes even brighter, and the temperature of the east end of the optical fiber that receives the light becomes high (for example, 500 to 600
During long-term use, the optical fiber's east end face becomes deformed or devitrified, resulting in a decrease in brightness. Another object of the present invention is to reduce the Pbo content by replacing P in the core glass with Bao or the like, in order to eliminate the above-mentioned drawbacks.
The purpose of the present invention is to provide a core glass for an endoscope optical fiber east which has a heat resistance temperature higher by, for example, about 100 qo, has less deformation and devitrification of the end face of the optical fiber east, and can be used for a long time. JP-A-53-60240 and JP-A-54-872 have already discussed improving the transmittance of optical fibers by reducing the P content to zero.
36, but the content of Pbo is set to zero,
When Ca○ is used as an essential component, the viscosity changes greatly with respect to temperature, resulting in poor workability, and it is extremely difficult to produce optical fibers with small seats and strict dimensional accuracy, such as optical fibers for endoscopes. The present invention relates to a core glass for optical fibers in endoscopes, which is characterized by having the following composition in terms of weight ratio.

35.0%<Sj○2く47.0% 1.0%く母0 く21.5% 1.0%くPb○ <21.5% 7.0%<Zn○ <30.0% 8.0く(Na20,K20,Li20の一または二以
上の合計)<13・9% Si02は35.0%以下の場合は耐水性、耐酸性が悪
くなって実際に使用不可能となる。
35.0%<Sj○2ku47.0% 1.0%ku21.5% 1.0%kuPb○ <21.5% 7.0%<Zn○ <30.0% 8 .0 (total of one or more of Na20, K20, Li20)<13.9% If Si02 is 35.0% or less, water resistance and acid resistance deteriorate and it becomes practically unusable.

Si02が47.0%以上の場合は屈折率ndが小とな
りすぎる。内視鏡用光学繊維の芯ガラスとしては開口数
の関係から少くとも屈折率ぬは1.55以上を必要とす
る。母○が1.0%以下の場合には屈折率ndが小とな
りすぎる。母○が21.5%以上の場合は温度に対する
粘度の変化が大となりすぎる。Pb0が1.0%以下の
場合は、屈折率ndが小となり、加工性が悪くなる。
When Si02 is 47.0% or more, the refractive index nd becomes too small. The core glass of the optical fiber for endoscopes must have a refractive index of at least 1.55 due to the numerical aperture. If the value of ○ is 1.0% or less, the refractive index nd becomes too small. When the value of ○ is 21.5% or more, the change in viscosity with respect to temperature becomes too large. When Pb0 is 1.0% or less, the refractive index nd becomes small and the workability deteriorates.

Pb0が21.5%以上の場合は着色のむらを生じやす
い。又X線照射により着色しやすい、又光学繊維東の端
面の耐熱温度が低下する。Zm0が7.0%以下の場合
は屈折率ndが4・となりすぎる。Zn○が30.0%
以上の場合は失透傾向が大となる。Na2,K20,L
i20の一つまたは二つ以上の合計が8.0%以下の場
合は熱膨脹係数が小となりすぎる。
When Pb0 is 21.5% or more, uneven coloring tends to occur. Furthermore, it is easy to be colored by X-ray irradiation, and the heat resistance temperature of the east end of the optical fiber is lowered. When Zm0 is 7.0% or less, the refractive index nd becomes too high as 4. Zn○ is 30.0%
In the above cases, the tendency to devitrify increases. Na2, K20, L
If the sum of one or more i20 is less than 8.0%, the coefficient of thermal expansion becomes too small.

Na20,K20,Li20の一つ又は二つ以上の合計
が13.9%以上の場合熱膨脹係数が大となりすぎ、ま
たガラスの耐風化性が低下する。また(範○十Pb○十
Zn○)が28.0%以下になると屈折率ndが小とな
りすぎて望ましくない。この池必要に応じて母○の一部
または大部分をSのにて置換してもよい。AI203,
B203などは約5.0%程度ならば本発明の特徴を損
うことなく添加することができる。
If the total of one or more of Na20, K20, and Li20 is 13.9% or more, the coefficient of thermal expansion becomes too large and the weathering resistance of the glass decreases. Furthermore, if (range ○ 10 Pb ○ 10 Zn ○) is less than 28.0%, the refractive index nd becomes too small, which is undesirable. If necessary, part or most of the mother ○ may be replaced with S. AI203,
B203 and the like can be added in an amount of about 5.0% without impairing the features of the present invention.

また清澄剤としてAs203,Sb203などを少量添
加する。第1表、第2表は本発明の実施例を示す。
Also, a small amount of As203, Sb203, etc. is added as a clarifying agent. Tables 1 and 2 show examples of the present invention.

表中の転位点は粘度が約1び3ポイズにおける温度、屈
折点は粘度が約1ぴ2ポィズにおける温度、耐水性およ
び耐酸性(粉末法)は試料を粒度420〜59岬に粉砕
し、メチルアルコールで洗浄した後乾燥させる。そして
この粉末試料の比重グラムを溶出用白金篭に入れる。次
にこれを試験溶液が入った、石英ガラス製丸底フラスコ
に入れ、沸騰水浴中で60分間処理したあと乾燥し、乾
燥後の試料の重量減を%で示した値である。耐水性の場
合は試験溶液として蒸留水(pH=6.5〜7.5)を
用い、耐酸性の場合は試験溶液として1/10皿硝酸(
PH=約2.2)を使用して試験する。以上述べた例は
主として芯ガラスに比較的高い屈折率のガラスを用い、
被覆ガラスに比較的低い屈折率のガラスを用いた二重光
学繊維東であるが、二重光学繊維の最外側に化学薬品に
侵飽されやすいガラス層を被覆した三重光学繊維東の芯
ガラスについても全く同じ効果を奏するものである。
In the table, the transition point is the temperature at which the viscosity is approximately 1 to 3 poise, the inflection point is the temperature at which the viscosity is approximately 1 to 2 poise, and the water resistance and acid resistance (powder method) are determined by pulverizing the sample to a particle size of 420 to 59 cape. Wash with methyl alcohol and dry. Then, the specific gravity gram of this powder sample is placed in a platinum cage for elution. Next, this was placed in a quartz glass round-bottomed flask containing the test solution, treated in a boiling water bath for 60 minutes, and then dried.The value is the weight loss of the sample after drying in %. For water resistance, use distilled water (pH = 6.5 to 7.5) as the test solution, and for acid resistance, use 1/10 plate nitric acid (
pH=approximately 2.2). The examples described above mainly use glass with a relatively high refractive index as the core glass,
Double Optical Fiber East uses glass with a relatively low refractive index for the coating glass, but regarding the core glass of Triple Optical Fiber East, the outermost layer of the double optical fiber is coated with a glass layer that is easily eroded by chemicals. also has exactly the same effect.

第1表 組成は重量努にて示す 第2表 組成は重量努にて示すTable 1 Composition is shown by weight Table 2 Composition is shown by weight

Claims (1)

【特許請求の範囲】 1 重量比にて下記の組成よりなることを特徴とする内
視鏡用光学繊維の芯ガラス。 35.0%<SiO_2<47.0% 1.0%<B_aO<21.5% 1.0%<PbO<21.5% 7.0%<ZnO<30.0% 8.0%<(Na_2O,K_2O,Li_2Oの 一
または二以上の合計)<13・9%0%≦Al_2O_
3<5.0% 0%≦B_2O_3<5.0% 0%≦SrO<10.0%
[Claims] 1. A core glass for an optical fiber for an endoscope, characterized by having the following composition by weight: 35.0%<SiO_2<47.0% 1.0%<B_aO<21.5% 1.0%<PbO<21.5% 7.0%<ZnO<30.0% 8.0%<( Total of one or more of Na_2O, K_2O, Li_2O)<13.9%0%≦Al_2O_
3<5.0% 0%≦B_2O_3<5.0% 0%≦SrO<10.0%
JP55182443A 1980-12-23 1980-12-23 Optical fiber core glass for endoscopes Expired JPS6024060B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55182443A JPS6024060B2 (en) 1980-12-23 1980-12-23 Optical fiber core glass for endoscopes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55182443A JPS6024060B2 (en) 1980-12-23 1980-12-23 Optical fiber core glass for endoscopes

Publications (2)

Publication Number Publication Date
JPS57106538A JPS57106538A (en) 1982-07-02
JPS6024060B2 true JPS6024060B2 (en) 1985-06-11

Family

ID=16118350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55182443A Expired JPS6024060B2 (en) 1980-12-23 1980-12-23 Optical fiber core glass for endoscopes

Country Status (1)

Country Link
JP (1) JPS6024060B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1106585A1 (en) 1999-12-04 2001-06-13 Schott Glas Optical glass containing zinc

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1106585A1 (en) 1999-12-04 2001-06-13 Schott Glas Optical glass containing zinc
DE19958522A1 (en) * 1999-12-04 2001-06-21 Schott Glas Optical glasses containing zinc
DE19958522B4 (en) * 1999-12-04 2004-04-08 Schott Glas Optical glasses containing zinc

Also Published As

Publication number Publication date
JPS57106538A (en) 1982-07-02

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