JPH03107105A - Optical fiber clad material - Google Patents

Abstract

PURPOSE:To obtain the clad material having good thermal stability by consisting the material of a copolymer of a prescribed ratio of fluoroalkyl methacrylate having a prescribed compsn. and a prescribed ratio of N-alkyl maleimide having a prescribed compsn. CONSTITUTION:This clad material is constituted of the copolymer contg. 70 to 99.8mol% fluoroalkyl methacrylate unit expressed by formula I and 30 to 0.2mol% N-alkyl maleimide expressed by formula II. In the formula I, R1: H or F, m: 1 or 2, n: 4 to 10 integer. In the formula II, R2: a group selected from the group of butyl, ethyl, propyl, isopropyl, butyl, sec-butyl, tert-butyl, hexyl, cyclohexyl. The thermal stability is extremely improved in this way as compared with the sheath material of the conventional alkyl methacrylate fluoride system and, therefore, the optical fiber is stably produced and the optical fiber having the excellent long-term heat resistance is obtd.

Description

DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a low refractive index optical fiber cladding material with excellent thermal stability.

[Prior Art] Optical fibers are generally composed of a combination of two materials: a core and a cladding having a lower refractive index than the core.

The core is made of quartz, multi-component glass, or a highly transparent resin such as polymethyl methacrylate.

On the other hand, the cladding needs to have a lower refractive index than the core material in order to trap light inside the core.
Fluorine-containing resins are widely used.

Examples of fluorine-containing resins include optical cladding materials with a quartz core, and fluoroethylene/fluoropropylene copolymers (Applied Optics, 14°156 (1975)).
Vinylidene fluoride/vinylidene fluoride/
Tetrafluoroethylene copolymer (Japanese Patent Publication No. 63-671
64), or hexafluoroacetone/vinylidene fluoride copolymer (
A method using Japanese Patent Laid-Open No. 61-22305) is known.

However, while these resins have excellent mechanical properties, thermal stability, and solvent resistance, they are crystalline and have poor transparency. In particular, films that are rapidly cooled after melting or cast from a solvent can be obtained in a transparent state, but they have the serious drawback that as the temperature increases, crystallization progresses and transparency is lost. .

For example, the maximum operating temperature of a plastic optical fiber with a core made of a polymer mainly composed of polymethyl methacrylate and a cladding made of vinylidene fluoride/tetrafluoroethylene copolymer is approximately 70°C, and changes in the form of the cladding material have an effect. This is because they are doing so.

In this way, even if transparency can be achieved by special measures during polymer shaping, the transparency will be impaired by stimuli such as heat during use.

Therefore, it had a serious effect on the performance of the optical fiber, and was not fully satisfactory as a cladding material for an optical fiber.

On the other hand, fluoroalkyl methacrylate polymers have been used to improve the transparency and increase the service temperature of optical fiber cladding materials.

For example, a (meth)acrylate/methyl methacrylate copolymer having a linear fluoroalkyl group is used as a cladding material for an optical fiber whose core is a polymer mainly composed of polymethyl methacrylate (Japanese Patent Publication No. 43-8978), or Long chain fluoroalkyl methacrylate (40~
70% by weight), a short-chain fluoroalkyl methacrylate (20 to 50% by weight), and a terpolymer of methyl methacrylate (Japanese Patent Application Laid-Open No. 62-265606).

However, methacrylate polymers are generally amorphous polymers, and although they are characterized by excellent transparency, they have the disadvantage that the polymers decompose when exposed to heat. For this reason, there is a problem that viscosity decreases and foaming tends to occur during melt extrusion, making it impossible to stably produce optical fibers.

In order to improve thermal stability, copolymerization with fluoroacrylate (Japanese Patent Application Laid-open No. 79704/1983) has been attempted. Although fluoroacrylate has a lower glass transition temperature (Tg) than the corresponding fluoromethacrylate and has improved thermal decomposition characteristics, it has the problem of lowering the heat resistance of the polymer, and is not fully satisfactory.

[Problems to be Solved by the Invention] The present inventors have arrived at the present invention as a result of intensive studies on optical fiber cladding materials that do not have the above-mentioned drawbacks.

An object of the present invention is to provide an optical fiber cladding material having a low refractive index and improved thermal stability and heat resistance.

[Means to solve the problem] The present invention has the following configuration.

(1) Contains 70 to 99.8 mol% of fluoroalkyl methacrylate units represented by the following general formula [II1,
An optical fiber cladding material comprising a copolymer containing 30 to 0.2 mol% of N-alkylmaleimide units represented by the following general formula [II].

(In formula I, R1 is H or F, m is 1 or 2
．． (n is an integer from 4 to 10) (In formula (1), R2 is selected from the group of methyl, ethyl, propyl, isopropyl butyl, 5ec-butyl, tert-butyl, hexyl, and cyclohexyl.) (2) In the following general formula [I] Contains 70 to 99.8 mol% of fluoroalkyl methacrylate units represented by the following formula [II], 20 to 0.2 mol% of N-alkylmaleimide units represented by the following general formula [II], and 10 to 29 mol% of methyl methacrylate units. An optical fiber cladding material comprising a copolymer containing .8 mol%.

H3 (In formula I, R1 is H or F, m is 1 or 2
゜n is an integer from 4 to 10) (In the formula (■), R2 is selected from the group of methyl, ethyl, propyl, isopropyl butyl, 5ec-butyl, tert-butyl, hexyl, and cyclohexyl.) The details of the present invention are as follows. explain.

The optical fiber cladding material of the present invention contains 70 to 99.8 mol% of the fluoroalkyl methacrylate units represented by the general formula [I] and N-alkylmaleimide units represented by the general formula [I]. It is composed of a copolymer containing 30 to 062 mol%.

Generally, the higher the fluorine content of a polymer, the lower the refractive index, but the refractive index of fluoroalkyl methacrylate can be lowered by increasing the fluorine content of the fluoroalkyl group.

On the other hand, when the fluoroalkyl methacrylate unit becomes a long chain, the glass transition temperature of the homopolymer decreases, and the polymer has the disadvantage of being sticky even at room temperature.

In the present invention, the fluorine content is 48% by weight or more in order to maintain a low refractive index. That is, the number of fluorine atoms in the fluoroalkyl unit is 8 or more. This allows the refractive index of the homopolymer to be 1.39 or less.

On the other hand, when the number of carbon atoms in the fluoroalkyl group is 12 or more and the number of fluorine atoms is 20 or more, the homopolymer cannot be used because its transparency is significantly impaired.

The reason for the loss of transparency is thought to be that crystallization of the fluoroalkyl group becomes more likely to occur.

On the other hand, the optical fiber cladding material of the present invention requires an N-alkylmaleimide monomer component.

If the N-alkylmaleimide unit is present in an amount of 30 mol % or more, the flexibility of the polymer will be impaired and it cannot be used as a cladding material.

By using N-alkylmaleimide units as a constituent component of the polymer, there are two major effects: increasing the glass transition temperature of the clad material and suppressing thermal decomposition.

When acrylate is used as a copolymerization component, thermal decomposition can be suppressed, but there is a problem in that it lowers the glass transition temperature of the polymer.

The most preferable range of N-alkylmaleimide unit component content is 20 mol% or less and 1 mol% or more.

N-alkyl substituents include methyl and ethyl.

Propyl, isopropyl, butyl, 5ec-butyl, t
selected from the group of ert-butyl, hexyl and cyclohexyl.

The most preferred N-substituent is propyl.

These are isopropyl, butyl, 5ec-butyl, and cyclohexyl.

Aromatic N-substituted maleimides cannot be used because they have a high refractive index and the monomers are colored. Even aromatic compounds such as pentafluorophenyl, in which the resonance effect of the aromatic ring is substantially inhibited by the electron-withdrawing property of the fluorine atom, can be used.

Furthermore, fluoroalkyl groups such as trifluoromethyl, trifluoroethyl, tetrafluoropropyl, hexafluoropropyl can be used as N-substituents.

Further, the present invention contains 70 to 99.8 mol% of the fluoroalkyl methacrylate units represented by the general formula [I], and 20 to 0.2% of the N-alkylmaleimide units represented by the general formula [II]. Contains 10 to 29 mol% of methyl methacrylate (hereinafter abbreviated as MMA) units.
．． It is composed of a copolymer containing 8 mol%.

MMA is effective in imparting flexibility and adhesion to the optical fiber core to the copolymer. If the amount is less than MMAIO mole %, the effect is not sufficient from the viewpoint of imparting flexibility and adhesion to the cladding material.

N-alkylmaleimide is an essential component for imparting thermal stability and heat resistance, and is required in an amount of 0.2 mol% or more.

In other words, in order to impart flexibility and adhesion without impairing heat resistance to a polymer with a low refractive index and excellent thermal stability, MM
A is required as a structural unit of 10 mol % to 29.8 mol %.

The optical fiber cladding material of the present invention has the above-mentioned general formula [I
] In addition to the fluoroalkyl methacrylate unit represented by the formula [II], the N-alkylmaleimide unit represented by the general formula [II], and the MMA unit, a third component may be contained within a range that does not impede the effects of the present invention.

In the present invention, when producing a polymer, it is polymerized using a radical polymerization catalyst and, if necessary, a molecular weight regulator.

As the polymerization method, bulk polymerization, suspension polymerization, emulsion polymerization, or solution polymerization can be used.

In bulk polymerization or solution polymerization, it is also preferable to use a method in which a monomer mixture is continuously supplied to the polymerization step, polymerized, and then volatiles are removed in a volatiles removal step to produce a polymer. can.

At that time, it can also be sent to an optical fiber spinning process and melted and co-extruded with the core to produce an optical fiber.

The optical fiber using the cladding material of the present invention is coated with polyethylene, polypropylene, a copolymer thereof, or a blend thereof in the coating process.

Olefinic polymers containing organic silane groups, ethylene-vinyl acetate, polyvinyl chloride, polyvinylidene fluoride,
Nylon resin, polyester resin.

Nylon elastomer Can be coated with a resin such as polyester elastomer or urethane and made into a cord. If the coating temperature is 240° C. or lower, the optical fiber can be processed without impairing its light transmission performance.

Furthermore, after melt extruding with the core, the cladding material can be fused at a temperature higher than the glass transition temperature of the cladding material to form a sheet.

Alternatively, a multicore die can be used to extrude into a sea-island structure in which the core material forms islands and the cladding material forms seas.

Furthermore, since the clad material of the present invention has excellent solvent resistance, it is possible to form a coating film by applying a resin solution with excellent heat resistance, a resin solution with high adhesiveness, or a solution containing a colored dye or fluorescent dye. You can also do it. Furthermore, it is also possible to fabricate the optical fiber into a generally planar heating element.

[Action of the invention] In the present invention, fluoroalkyl methacrylate and N-
Copolymerization of alkylmaleimide has the following effects.

■ Increase heat distortion temperature.

■ Improve chemical stability due to heat and light.

■ Improves transparency and has a low refractive index.

■ Improve solvent resistance.

■ Improve flexibility and improve adhesion to the core.

[Example J The abbreviations and chemical composition details of each monomer used in the example are shown below.

Fluoroalkyl methacrylate monomer 17FM: CH3 CH2= C cmo-(CH2) 1 (CF2) Fluoroalkyl methacrylate monomer 8 FM: CH3 CH2= C C-0-CH2 1 (CF2) Fluoroalkyl methacrylate monomer 4 FM: CH3 CH2 Horse C-0-CH2 No (CF2) Monomer CH-MID+ (5) (6) N-cyclohexylmaleimide monomer ipr-MID: N-isopropylmaleimide monomer MMA: Methyl methacrylate implementation Example 1 Monomer 17FM 95 parts (86.5 mol%) Cyclohexylmaleimide 5 parts (13.5 mol%) Azobisisobutylnitrile 0.01 part n-butyl mercaptan 0.005 parts were charged into a glass ampoule. After removing dissolved oxygen, the mixture was heated in a sealed tube 60'C for 16 hours and at 100° C. for 8 hours to complete polymerization. After removing the polymer from the glass ampoule and crushing it in liquid nitrogen,
Vacuum drying was performed at 115° C. for 48 hours to obtain a polymer.

As a thermal stability test, heat at 240°C, and after 1 part and 60
Measure the polymer viscosity after 10 minutes, and
The viscosity retention rate after 0 minutes was determined.

Using this polymer as a cladding, an optical fiber was obtained by composite spinning using melt coextrusion.

The outer diameter of the obtained optical fiber was 1000μ, and the thickness of the cladding was 9μ.

The heat resistance of optical fiber is evaluated by heating 10 m of optical fiber at 90°C in an oven for 500 hours, measuring the amount of emitted light when using a red LED as a light source, and comparing it with a blank to determine the light amount retention rate. did.

The bending characteristics were evaluated by continuously bending the optical fiber 180 times with a bending radius of 5 mm under a load of 700 g, and measuring the number of times it took to break. Table 1 shows the characteristics of the cladding material and the characteristics of the optical fiber using the cladding material.

The properties of the clad material were that it had a low refractive index, excellent thermal stability, and no problems with heat resistance.

The properties of the optical fiber were also excellent in light transmission, heat resistance, and bending properties.

Examples 2 to 5 Clad materials having the compositions shown in Table 1 were produced in the same manner as in Example 1.

As shown in Table 1, both the properties of the cladding material and the properties of the optical fiber using the cladding material showed excellent results.

Comparative Example 1 A test was carried out in the same manner as in Example 1 except that 17FM used in Example 1 was used alone, and the results are shown in Table 1.

When the clad material was heated at 240° C. for 60 minutes, the viscosity decreased so much that it could not be measured. The glass transition temperature is determined by DSC (
It was not detected by a differential scanning calorimeter (differential scanning calorimeter), but developed tackiness at temperatures above 50°C, and could not be used as an optical fiber cladding material.

Comparative Example 2 As monomers, the above 17FM (50 mol%), the above i p
The same procedure as in Example 1 was carried out except that r-MID (50 mol %) was used, and the results are shown in Table 1.

The clad material was slightly cloudy and a brittle polymer. Although it has excellent heat resistance as an optical fiber, it has poor light transmission performance and flexibility, and cannot be used as an optical fiber cladding material.

Comparative Example 3 As monomers, the above 8FM (50 mol%), the above 4FM (
Example 1 was repeated except that 50 mol %) was used, and the results are shown in Table 1.

Clad material has poor thermal stability and foaming is observed.

Both the heat resistance and flexibility of the optical fiber were unsatisfactory.

[Effects of the Invention] The optical fiber cladding material of the present invention has significantly improved thermal stability compared to conventional fluorinated alkyl methacrylate sheath materials, and therefore optical fibers can be stably manufactured. In addition, since there are extremely few residual monomers generated by thermal decomposition,
Excellent long-term heat resistance.

Furthermore, since the glass transition temperature can be raised, it does not develop tackiness even at higher temperatures, exceeding the operating temperature of conventional optical fibers.

Claims (2)

[Claims] (1) Contains 70 to 99.8 mol% of fluoroalkyl methacrylate units represented by the following general formula [I],
An optical fiber cladding material comprising a copolymer containing 30 to 0.2 mol% of N-alkylmaleimide units represented by the following general formula [II]. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...[I] (In formula I, R_1 is H or F, m is 1 or 2, and n is an integer from 4 to 10) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ ...[II] (In formula II, R_2 is methyl, ethyl, propyl,
selected from the group of isopropyl butyl, sec-butyl, tert-butyl, hexyl, cyclohexyl. ) (2) Contains 70 to 99.8 mol% of fluoroalkyl methacrylate units represented by the following general formula [I],
It is characterized by being composed of a copolymer containing 20 to 0.2 mol% of N-alkylmaleimide units represented by the following general formula [II] and 10 to 29.8 mol% of methyl methacrylate units. Optical fiber cladding material. ▲There are mathematical formulas, chemical formulas, tables, etc.▼...[I] (In formula I, R_1 is H or F, m is 1 or 2, and n is an integer from 4 to 10) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ ...[II] (In formula II, R_2 is methyl, ethyl, propyl,
selected from the group of isopropyl butyl, sec-butyl, tert-butyl, hexyl, cyclohexyl. )