JPS60118808A - Optical transmission body - Google Patents

Optical transmission body

Info

Publication number
JPS60118808A
JPS60118808A JP58227345A JP22734583A JPS60118808A JP S60118808 A JPS60118808 A JP S60118808A JP 58227345 A JP58227345 A JP 58227345A JP 22734583 A JP22734583 A JP 22734583A JP S60118808 A JPS60118808 A JP S60118808A
Authority
JP
Japan
Prior art keywords
polymer
formula
core
optical transmission
transmission body
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
JP58227345A
Other languages
Japanese (ja)
Inventor
Akira Omori
晃 大森
Nobuyuki Tomihashi
信行 富橋
Takahiro Kitahara
隆宏 北原
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.)
Daikin Industries Ltd
Original Assignee
Daikin Industries Ltd
Daikin Kogyo 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 Daikin Industries Ltd, Daikin Kogyo Co Ltd filed Critical Daikin Industries Ltd
Priority to JP58227345A priority Critical patent/JPS60118808A/en
Publication of JPS60118808A publication Critical patent/JPS60118808A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/80Non-oxide glasses or glass-type compositions
    • C03B2201/84Halide glasses other than fluoride glasses, i.e. Cl, Br or I glasses, e.g. AgCl-AgBr "glass"
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/80Non-oxide glasses or glass-type compositions
    • C03B2201/86Chalcogenide glasses, i.e. S, Se or Te glasses

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)

Abstract

PURPOSE:To obtain an optical transmission body having high softening temp. and good flexibility by using a polymer having methyl-alpha-fluoracrylate and methyl methacrylate as a polymer unit for the core thereof and a polymer contg. fluoroalkyl-alpha-fluoroacrylate as a polymer unit for the cladding. CONSTITUTION:An optical transmission body is manufactured by using a polymer contg. preferably >=70mol% the structural unit expressed by the formula I (X is F or CH3) as a core and a polymer contg. >=10mol% the structural unit expressed by the formula II (Rf is fluoroalkyl) as a cladding. The optical transmission body of which the core has 1.47-1.51 refractive index and the cladding 1.36-1.43 and which has good flexibility, high softening point and excellent gasoline resistance is obtd.

Description

【発明の詳細な説明】 本発明は、プラスチック系光伝導体に関する。[Detailed description of the invention] The present invention relates to plastic-based photoconductors.

従来、メチルメタクリレート恵合体を芯とし、フルオロ
アルキルメククリレート重合体tJIQとしたフ”ラス
チック系光伝導体は公知である(特公昭54−2430
2号公報)。しかしながら、この光伝導体は司撓性に難
点があり、また長時間高温下におか扛るとその光透過度
は著しく低下してしまい、さらには車輌等に設置したと
きガソリン等の燃料に侵されやすいという問題も有して
いる。
Conventionally, plastic photoconductors with a core of methyl methacrylate polymer and a fluoroalkyl methacrylate polymer tJIQ have been known (Japanese Patent Publication No. 54-2430).
Publication No. 2). However, this photoconductor has problems with its flexibility, and its light transmittance decreases significantly if it is exposed to high temperatures for a long period of time.Furthermore, when it is installed in a vehicle, it is eroded by fuels such as gasoline. It also has the problem of being easily exposed.

′本発明の目的は、従来の1ラスチック系光伝導体より
も司撓性が良好で耐熱性にもすぐれ、さらK ガソリン
等にも侵されないフ”ラスナック系光伝導体全提供する
ことにおる。
'The object of the present invention is to provide a plastic optical conductor which has better flexibility and heat resistance than conventional single plastic optical conductors, and which is not eroded by K gasoline or the like. .

かかる本発明の要旨は、フ゛ラスチック糸クラッド型光
伝導体において、芯が式: X / −CH2−C− \ C0(X;H。
The gist of the present invention is to provide a plastic thread clad photoconductor in which the core has the formula: X/-CH2-C-\C0(X;H.

(式中、XはFまたはCH3を示す。)で表わされる構
造単位を有する■合体、鞘が式:%式% (式中、Rfはフルオロアルキル基を示す。)で表わさ
れる構造単位を有する重合体からなることを特徴とする
光伝導体である。
(In the formula, X represents F or CH3.) The union, sheath has a structural unit represented by the formula: % Formula % (In the formula, Rf represents a fluoroalkyl group.) A photoconductor characterized by being made of a polymer.

本発明に係る光伝導体の鞘成分重合体は、式(b)で表
わされる構造単位を10モル%以上含有することが、光
伝導体の可撓性を良好にする上で好ましく、また各成分
の■合体がそれぞれ式(a)または式(b)で表わされ
る構造単位ラフ0モル%以上含有することが、光伝導体
の軟化温度100°C以上に向上させたり光伝導体の透
明性を保つ上で、またガソリン等に耐性を持たせる上で
好ましい。
The sheath component polymer of the photoconductor according to the present invention preferably contains 10 mol% or more of the structural unit represented by formula (b) in order to improve the flexibility of the photoconductor. Containing 0 mol% or more of rough structural units represented by formula (a) or formula (b) in the combination of the components improves the softening temperature of the photoconductor to 100°C or higher and improves the transparency of the photoconductor. This is preferable in terms of maintaining the temperature and resistance to gasoline and the like.

上記構造単位(a)を有する芯成分血合体は、通常/ CH2= C \ 0OCH3 (式中、Xは前記と同じ。) で表わされる1#量体のみを重合するか、あるいはこの
単量体とエチルメタクリレート、メチル−a−フルオロ
アクリレート、メタクリル酸等のアクリル酸誘導体と全
共重合すること罠よって得ることができる。なお、さら
に共単量体として他のエチレン性不飽和化合物を共重合
することも可能である。
The core component blood complex having the above structural unit (a) is usually produced by polymerizing only the 1#mer represented by /CH2=C\0OCH3 (wherein, X is the same as above), or by polymerizing this monomer. and an acrylic acid derivative such as ethyl methacrylate, methyl-a-fluoroacrylate, or methacrylic acid. In addition, it is also possible to further copolymerize other ethylenically unsaturated compounds as comonomers.

上記構造単位(b)を有する鞘成分重合体は、通常酸二
 F / C夏12=C \ 0ORf (式中、R7は前記と同じ。) で表わされる単量体のみを重合するが、あるいけこの単
量体とメチル−α−フルオロアクリレート、メタクリル
酸メチル、メタクリル酸等のアクリル酸誘導体とを共重
合することによって得ることができる。なお、さらに共
単量体として他のエチレン性不飽和化合物を共重合する
ことも可能である。
The sheath component polymer having the above structural unit (b) usually polymerizes only the monomer represented by the following formula (wherein, R7 is the same as above). It can be obtained by copolymerizing a mushroom monomer with an acrylic acid derivative such as methyl-α-fluoroacrylate, methyl methacrylate, or methacrylic acid. In addition, it is also possible to further copolymerize other ethylenically unsaturated compounds as comonomers.

上記芯あるいは鞘成分重合体は、いずれも塊状、溶液、
懸濁、乳化重合等、一般に採用てれている重合方法で重
合して製造することができる。重合開始剤としては、塊
状、溶液および懸濁重合においてはアゾ糸化合物または
有機過酸化物が用いられ、例えばアゾビスイソブチロニ
トリル、イソブチリルパーオキシド、オクタノイルパー
オキシド、ジーイソーブIUビルバーオキシーン゛−カ
ーボネート、または式(CI (CF2 CFC71)
2 C:F2 Coo)2 、(H(CF2CF2 )
3 Coo)2および(CJ CF2 CF2 COO
)2で表わされる含フツ素有機過酸化物等が好ましく用
いられる。乳化重合においては、過硫酸塩、例えば過硫
酸アンモニウム、過硫酸カリまたはこれら過硫酸塩辱の
酸化剤、亜硫酸ソーダ等の還元剤および硫酸鉄(社)等
の遷移金属の塩類のレドックス開始剤か用いられる。
The above-mentioned core or sheath component polymers may be in the form of lumps, solutions,
It can be produced by polymerization using commonly used polymerization methods such as suspension and emulsion polymerization. As polymerization initiators, azo thread compounds or organic peroxides are used in bulk, solution and suspension polymerizations, such as azobisisobutyronitrile, isobutyryl peroxide, octanoyl peroxide, G-Isorb IU bilber oxide, etc. Sheen-carbonate, or formula (CI (CF2 CFC71)
2C:F2Coo)2, (H(CF2CF2)
3 Coo)2 and (CJ CF2 CF2 COO
) A fluorine-containing organic peroxide represented by 2 is preferably used. In emulsion polymerization, persulfates such as ammonium persulfate, potassium persulfate or oxidizing agents such as these persulfates, reducing agents such as sodium sulfite, and redox initiators such as salts of transition metals such as iron sulfate are used. It will be done.

塊状、溶液または懸濁重合において、■合体の熱分解温
度の向上や分子量分布の調整の目的で、メルカプタン類
等の連鎖移動利金用いることが好ましい。連鎖移動剤を
用いる場合の連鎖移動剤の添加割合は、小量体100重
量部に対し通常0.01〜1重量都である。
In bulk, solution or suspension polymerization, it is preferable to use a chain transfer agent such as mercaptans for the purpose of (1) increasing the thermal decomposition temperature of the polymer and adjusting the molecular weight distribution. When a chain transfer agent is used, the addition ratio of the chain transfer agent is usually 0.01 to 1 part by weight per 100 parts by weight of the small polymer.

溶液J1f合で■(合体を製造する際に用いられる有ル
、メチルイソグチルケトン、ア七ト二トリル、アセトン
、ジメチルホルムアミド等炭化水素系溶媒が例示できる
Examples of hydrocarbon solvents used in the production of solution J1f include (2), methyl isobutyl ketone, a7tonitrile, acetone, and dimethylformamide.

重合温度は通常0〜100℃の範囲で上記重合開始剤の
分解温度との関係で決められるが、多くの場合10〜8
0゛Cの範囲が好ましく採用される。
The polymerization temperature is usually in the range of 0 to 100°C, and is determined in relation to the decomposition temperature of the polymerization initiator, but in most cases it is in the range of 10 to 8°C.
A range of 0°C is preferably adopted.

m合圧力は0〜50Kg/dゲージの範囲が採用で上記
重合反応で調製した芯または鞘成分重合体のゲルパーミ
ェーションで測定した分子量は、いずれも通常20万〜
500万、軟化温度もいずれも通常100〜150℃で
おるが、屈折率は通常芯成分重合体が1.47〜1.5
1であるのに対し、鞘成分重合体はl、36〜1.43
である。
The combined pressure is in the range of 0 to 50 kg/d gauge, and the molecular weight measured by gel permeation of the core or sheath component polymer prepared by the above polymerization reaction is usually 200,000 to 200,000.
5 million, and the softening temperature is usually 100 to 150°C, but the refractive index of the core component polymer is usually 1.47 to 1.5.
1, whereas the sheath component polymer has l, 36 to 1.43
It is.

本発明に係る光伝導体は、通常芯あるいは鞘成分重合体
をそれぞれ別に加熱溶融し、ついで複合紡糸することに
よって製造される。
The photoconductor according to the present invention is usually produced by separately heating and melting the core or sheath component polymers, and then subjecting them to composite spinning.

この光伝導体の直径は、通常100〜500μmでその
うち鞘の厚みはダ〜5otanである。
The diameter of this photoconductor is usually 100 to 500 μm, and the thickness of the sheath is about 5 to 50 μm.

次に不究明に作る光伝導体(実施例1〜7)および比較
例先広4体の調製例ならひに試験例を示す。
Next, a test example of the preparation of photoconductors (Examples 1 to 7) made in an unknown manner and four comparative examples with a wide tip will be shown.

調製例 (実施例1〜72よび比較例)第1表に示す各
単量体音50°Cで3時間塊状重合し、芯あるいは鞘成
分重合体を調製した。
Preparation Examples (Examples 1 to 72 and Comparative Examples) Each monomer shown in Table 1 was subjected to bulk polymerization at 50°C for 3 hours to prepare a core or sheath component polymer.

なお、この際単量体1(用重量部当すアゾビスイソプチ
ロニトリル0.05ii1部、11−ドデシルメルカフ
゛タン0.5重量部を使用した。
In this case, 1 part by weight of azobisisobutyronitrile and 0.5 part by weight of 11-dodecylmercaptan were used per part by weight of monomer 1.

上記得られた各成分重合体を用い、第1表に示す組合せ
で直径300μm1但し鞘岸み15μm1長ざ500闘
の光伝導体を、本発明に係る光伝導体は250°Cで、
比較例の重合体は250℃では熱分解し始めるため22
0°Cで、8 yiz /分の速度で複合紡糸しその後
180°Cで1.5倍に延伸した。
Using the respective component polymers obtained above, a photoconductor of 300 μm in diameter, 15 μm in sheath depth, and 500 μm in length was prepared using the combinations shown in Table 1. The photoconductor according to the present invention was heated at 250°C.
The polymer of the comparative example starts to thermally decompose at 250°C, so 22
The composite was spun at 0°C at a speed of 8 yiz/min and then stretched 1.5 times at 180°C.

光透過度および可撓性試験 上記調製した試料について、650〜680 nmの光
で紡糸直後と100℃の雰囲気下100時間放置後の光
透過度の測定を行った。またこの試料を種々の直径の鋼
棒にまきつけ、鞘にひひの入る最小怪をめるiJ撓注性
試験何った。結果を第1表に示す。
Light Transmittance and Flexibility Test The light transmittance of the sample prepared above was measured using light of 650 to 680 nm immediately after spinning and after being left in an atmosphere at 100° C. for 100 hours. In addition, this sample was wrapped around steel rods of various diameters, and an iJ bendability test was carried out to minimize the chance of the rod entering the sheath. The results are shown in Table 1.

(公人下會合、〕欠り〕こル魁く) 第1表 な訃、表中MMAはメチルメタクリレート、EMAはエ
チルメタクリレート、MFAffメチル−〇−フルオロ
アクリレート、MAはメタクリル酸、p lr p n
ペンタフルオロプロピル−α−フルオロアクリレート、
11 F Bは2.2.8.4.4−へキサフルオロブ
チル−a〜フルオロアクリレート、TFEI−J、 2
.2.2−1−リフルオロエチル−α−フルオロアクリ
レート、口FBMは2.2.8.4.4.4−ヘキサフ
ル刃」Jグチルメタクリレートを示す。
(Public figure meeting, [missing] this) Table 1. In the table, MMA is methyl methacrylate, EMA is ethyl methacrylate, MFAff methyl-〇-fluoroacrylate, MA is methacrylic acid, p lr p n
pentafluoropropyl-α-fluoroacrylate,
11 FB is 2.2.8.4.4-hexafluorobutyl-a-fluoroacrylate, TFEI-J, 2
.. 2.2-1-Lifluoroethyl-α-fluoroacrylate, FBM indicates 2.2.8.4.4.4-hexaful blade'J goutyl methacrylate.

耐ガソリン試験 力′ンリンの飽和蒸気ケみたした80°Cの恒温槽に、
1j11記火施例1〜7および比較例で調製した光伝導
体を入れ、500時間放置後光透過度をめたとこイ)、
実施例1〜7のものはほとんど光透過+Xの低−1・け
みられなかっfcが、比較例のものは光透過度が1)%
にhつ゛た。この比較例の先広2jJ、I4−の表面t
i11’+徽鏡で#M察しt(ところ、表面にl−1′
会小クラツクが入り、鞘が部分的に欠落していた。
Gasoline resistance test
1j11 The photoconductors prepared in Examples 1 to 7 and Comparative Examples were added, and the light transmittance was measured after standing for 500 hours).
Examples 1 to 7 have almost no fc of low light transmission +
I had a hard time. The surface t of the wide tip 2jJ and I4- of this comparative example
i11' + #M detected with a mirror (by the way, l-1' on the surface
It contained a kaiko kratsuku, and the scabbard was partially missing.

以上 特許出願人 ダイキン工業株式会社that's all Patent applicant: Daikin Industries, Ltd.

Claims (1)

【特許請求の範囲】 15 プラスナッチ糸クラッド型光伝導体において、芯
が式: %式%() (式中、XはFまたけCH3を示す。)で表わされる構
造単位を有する重合体、鞘が式: %式%() (式中、Rfはフルオロアルキル基を示ス。)で表わき
れる崩造単位ケ有する重合体からなることを特徴とする
光伝導体。 2、鞘が式(b)で表わされる構造単位を10モル%以
上含有する重合体である特許請求の範囲第1項記載の光
伝導体。 8、芯が式(a)で表わされる構造単位fc70モル%
以上含有する重合体、鞘が式(b)で表わ畑nる渦愈単
位全70モル%以上含有する重合体である特許請求の範
囲第1項または第2項記載の光伝導体。
[Claims] 15 In a plus-natch yarn clad type photoconductor, the core is a polymer having a structural unit represented by the formula: % formula % (in the formula, X represents F and CH3); A photoconductor characterized in that the sheath is made of a polymer having a collapsible unit represented by the formula: %(%) (wherein Rf represents a fluoroalkyl group). 2. The photoconductor according to claim 1, wherein the sheath is a polymer containing 10 mol% or more of the structural unit represented by formula (b). 8. Structural unit fc whose core is represented by formula (a) 70 mol%
3. The photoconductor according to claim 1, wherein the polymer sheath contains 70 mol% or more of vortex units represented by formula (b).
JP58227345A 1983-11-30 1983-11-30 Optical transmission body Pending JPS60118808A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58227345A JPS60118808A (en) 1983-11-30 1983-11-30 Optical transmission body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58227345A JPS60118808A (en) 1983-11-30 1983-11-30 Optical transmission body

Publications (1)

Publication Number Publication Date
JPS60118808A true JPS60118808A (en) 1985-06-26

Family

ID=16859343

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58227345A Pending JPS60118808A (en) 1983-11-30 1983-11-30 Optical transmission body

Country Status (1)

Country Link
JP (1) JPS60118808A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60250310A (en) * 1984-05-28 1985-12-11 Daikin Ind Ltd Clad material for optical fiber

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60250310A (en) * 1984-05-28 1985-12-11 Daikin Ind Ltd Clad material for optical fiber
JPH0251483B2 (en) * 1984-05-28 1990-11-07 Daikin Ind Ltd

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