EP0319572A1 - Aromatic ester carbonate polymer optical waveguides - Google Patents
Aromatic ester carbonate polymer optical waveguidesInfo
- Publication number
- EP0319572A1 EP0319572A1 EP88906580A EP88906580A EP0319572A1 EP 0319572 A1 EP0319572 A1 EP 0319572A1 EP 88906580 A EP88906580 A EP 88906580A EP 88906580 A EP88906580 A EP 88906580A EP 0319572 A1 EP0319572 A1 EP 0319572A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aromatic ester
- core
- carbonate
- linkages
- ester carbonate
- 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.)
- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/16—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one other macromolecular compound obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds as constituent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C08L69/005—Polyester-carbonates
Definitions
- This invention relates to novel polymer optical waveguides with higher use temperatures than previously known for polymer optical waveguides. More particularly, these polymer optical waveguides are based on aromatic ester carbonates.
- Polymer optical waveguides are generally comprised of optically clear polymers which transmit light. Such waveguides may be of various shapes.
- a polymer optical waveguide comprises a core of a material which transmits light, and a clad over the core which has a different refractive index than the core where the difference is such that the light waves do not pass through the cladding but instead are reflected back into the core of the waveguide.
- the light transmitted down polymer optical waveguides can be used for illumination or data transmission. In illumination uses, the optical waveguides are used to light up signs, in decorative objects and can be used to light up certain functional apparatus such as the dashboard of an automobile.
- Polymer optical waveguides must be optically clear with low attenuation, that is, little light loss as the light is transmitted down the fiber. Furthermore, polymer optical waveguides must withstand handling and bending during processing of the waveguides.
- polymer optical waveguides generally comprise cores of acrylics or styrenics, with claddings of acrylics or fluoropolymers. These materials generally have a relatively low use temperature, for example less than 90°C, and low resistance to harsh environments such as high humidity environments. In many potential uses for polymer optical waveguides, the polymers are exposed to high temperatures and/or harsh environments, i.e. humid environments. The present polymer optical waveguides are not able to tolerate such conditions.
- the invention is a polymer optical waveguide which comprises%
- the polymer optical waveguides of this invention are useful at higher temperatures than presently known optical waveguides. These polymer optical waveguides demonstrate low attenuation and are much more resistant to humidity and other hostile environments. Furthermore, these polymer optical waveguides demonstrate good ductility and are able to withstand normal handling and bending during fabrications of devices from polymer optical waveguides.
- An aromatic ester carbonate comprises a polymer with ester and carbonate functional groups, or linkages, along the backbone of the polymer, wherein such functional or linking groups link hydrocarbylene moieties.
- the hydrocarbylene moieties comprise arylene and the residue of bisphenolic compounds.
- Ester linkage refers herein to a functional group along the backbone of the polymer which corresponds to the formula
- Carbonate moieties as used herein refer to functional groups or linkages along the backbone of the polymer which corresponds to the formula
- core and claddings are often referred to and described by the percentage of ester and carbonate linkages in the backbone of the polymer.
- a particular core or clad with a stated percentage of carbonate or ester linkages may comprise a copolymer with the stated percentage of ester and carbonate linkages in the backbone, or it may be a blend of an aromatic ester carbonate and a polycarbonate to create a blend with the stated percentage of ester and carbonate linkages in the total blend.
- a copolymer with a stated ester and carbonate percentage in the backbone of the polymer is equivalent to a blend with the same percentage of ester and carbonate linkages.
- Arylene refers herein to moieties which comprise aromatic moieties with two bonds. Examples of such moieties include phenylene and biphenylene moieties.
- Phenylene moiety as used herein refers to ortho, meta, and para phenylene linkages, wherein meta and para linkages are preferred and most commonly found.
- the phenylene moiety is a mixture of the residue of terephthalic and isophthalic acid.
- the percentage of terephthalic acid to isophthalic acid moieties is from 80:20 to 20:80, more preferably from 80:20 to 50:50, and most preferably from 80:20 to 70:30. Percentages of ester to carbonate linkages are based on mole percent.
- the bisphenol moieties in the backbone of the aromatic ester carbonates may be the residue of any bisphenolic compound which may be reacted to prepare an aromatic ester carbonate.
- the polycar-bonates which may be blended with an aromatic ester carbonate to get a particular percentage of ester and carbonate linkages in the material may be any bisphenolic based polycarbonate.
- the aromatic ester carbonate comprises units which correspond to the formula
- R 1 is the residue of a bisphenol moiety
- R 2 is arylene
- z is a positive real number such that the molecular weight of the aromatic ester carbonate is between 4,000 and 200,000;
- R 2 is preferably phenylene.
- z is a positive real number such that the molecular weight of the aromatic ester carbonate is between 10,000 and 100,000, and even more preferably between 15,000 and 45,000.
- the polycarbonates which may be blended with the aromatic ester carbonates may be any polycarbonates known to the skilled artisan which will blend with the particular aromatic ester carbonate used.
- the bisphenolic based polycarbonates are preferred and more preferred polycarbonates comprise units which correspond to the formula
- R 3 at each occurrence is independently H, Cl, Br, or C 1 -C 4 alkyl
- R 4 is a direct bond, ⁇ arbonyl, -S-, -SO 2 -, -O-, a C 1 -C 12 divalent hydrocarbon, a C 1 -C 6 divalent fluorocarbon radical, or inertly substituted C 1 -C 6 divalent hydrocarbon radical;
- t is independently in each occurrence an integer of between 16 and 800.
- the bisphenols whose residues are found in the aromatic ester carbonate, i.e. R 1 preferably correspond to the formula
- R 3 is independently at each occurrence H, Cl, Br, or C 1 -C 4 alkyl
- R 4 is independently at each occurrence a direct bond, a carbonyl, -S-, -SO 2 -, -O-, a C 1 -C 6 divalent hydrocarbon, a C 1 -C 6 divalent fluorocarbon radical, or an inertly substituted C 1 -C 6 divalent hydrocarbon radical.
- R 3 is preferably hydrogen or C 1-4 alkyl, more preferably hydrogen or methyl, and most preferably hydrogen.
- R 4 is preferably C 1-6 hydrocarbylene, a direct bond, oxygen, or C 1-6 perfluorohydrocarbylene. Even more preferably, R 4 is C 1-6 alkylidene, oxygen, C 1-6 perfluoroalkylidene, or a direct bond. Even more preferably, R 4 is isopropylidene, CH 2 , oxygen, C(CF 3 ) 2 , or a direct bond. Most preferably, R 4 is isopropylidene.
- the most preferred bisphenol moiety is a bisphenol A moiety.
- Aromatic ester carbonates useful in this invention preferably have a total mole percent of ester linkages of between 0.5 and 95 percent, more preferably between 1 and 80 percent, and most preferably between 5 and 75 percent.
- Aromatic ester carbonates and their preparation are well known in the art. See, for example, U.S. Patent 4,330,662.
- the polycarbonates useful in this invention and their preparation are well known in the art. See, for example, Encyclopedia of Polymer Science and Technology, editor Mark et al., Interscience Division of John Wiley and Sons, New York, New York, 1969, Volume 10, pages 714-725.
- Blends of aromatic ester carbonates and polycarbonates may be prepared by methods well known in the art, preferred methods include solution and melt blending.
- the core of the polymer optical waveguides of this invention comprises an aromatic ester carbonate copolymer, or a blend of aromatic ester carbonates with polycarbonates.
- Such a core comprises the percentages of ester to carbonate linkages described hereinbefore.
- Such a core must be able to transmit light with acceptable attenuation for the particular use.
- acceptable attenuation level is dependent upon the particular use to which the optical waveguide is put. Generally, the higher the ester linkage percentage, the higher the use temperature.
- a clad useful in the polymer optical waveguides of this invention can be any polymer which adheres to the core polymer and has a lower refractive index than the aromatic ester carbonate or blend of the aromatic ester carbonate and bisphenol based polycarbonate.
- the adhesion must be such that during either use or handling of the optical waveguides, the cladding does not separate from the core.
- the polymer used for the cladding must have a lower refractive index so that as light passes down the core and is reflected or refracted in the direction of the core, the clad functions to reflect the light back into the core of the optical waveguide so that it may continue down the core.
- the difference in refractive index between the core and the clad is 0.016 or above.
- Preferable polymers useful as claddings comprise acrylics, aromatic ester carbonates, a blend of an aromatic ester carbonate with a polycarbonate, a polycarbonate, an imidized acrylic based polymer, or a fluoropolymer.
- the aromatic ester carbonates and blends of aromatic ester carbonates with polycarbonates wherein the ester linkage percentage is lower than that of the core will have a lower refractive index than that of the core, and thus be preferred for use as claddings in this invention. Such difference must be sufficient so that the light waves are reflected back into the core from the cladding.
- the choice of the particular polymer to be used as a cladding is dependent upon the particular composition of the core and the desired use temperature for the polymer optical waveguide.
- the polycarbonates useful for clads in this invention include those polycarbonates described hereinbefore.
- Fluoropolymer refers herein to polymers derived from monomers comprising unsaturation with fluorine substitution on the unsaturated carbons, and acrylics with fluorine substitution on saturated or unsaturated carbons.
- Preferred fluoropolymers include fluoroolefins and fluorinated acrylics.
- More preferable fluoropolymer clads include vinylidine fluoride based polymers or copolymers of vinylidine fluoride with tetrafluoroethylene or hexafluoropropylene.
- Preferred fluorinated acrylics include fluorinated polyalkylacrylates and fluorinated polyalkylmethacrylates.
- More preferred fluorinated acrylics include fluorinated polytrifluoro ethyl methacrylates or fluorinated polyalkylmethacrylates.
- Imidized acrylic based polymers include those described in U.S. Patent 4,246,374.
- Preferred acrylics include polymers which comprise 50 percent or more of polyalkylacrylates and polyalkylalkacrylates. More preferred acrylics include the polyalkylmethacrylates. Most preferred acrylics include polymethylmethacrylates. In the embodiment wherein the polymethyl methacrylate is used in higher temperature use optical waveguides, the polymethylmethacrylate is preferably a syndiotactic polymethylmethacrylate.
- Such syndiotactic polymethylmethacrylates are available from Rohm Corporation under the designation Rohm 8678 and Rohm 8H.
- the claddings of imidized acrylic based polymers, aromatic ester carbonates, and blends of aromatic ester carbonates with polycarbonates generally have higher use temperatures than do the acrylics or fluoropolymers.
- the polymer optical waveguides of this invention comprise
- such polymer optical waveguide comprises
- the polymer optical waveguides of this embodiment preferably have a use temperature of 140°C or above.
- Use temperature means herein that the polymer optical waveguide can be used at or above the stated temperature for extended periods without the polymer or the optical waveguide undergoing significant degradation.
- the polymer optical waveguide comprises
- the polymer optical waveguide comprises (A) the core comprises an aromatic ester carbonate or a blend of an aromatic ester carbonate and a polycarbonate wherein the total amount of ester linkages in the core is between 1 percent and 25 percent, with the remaining linkages being carbonate linkages; and
- such polymer optical waveguide comprises
- a most preferred cladding for this embodiment is an imidized acrylic based polymer.
- the polymer optical waveguides demonstrate a use temperature of 120°C or above.
- the polymer optical waveguides of this invention may be of any length, shape, or arrangement, known to one skilled in the art.
- the optical waveguides may be round, square, triangular, may be in the shape of a hollow light pipe wherein the core is a hollow light pipe and the clad surrounds the hollow light pipe core.
- the clad may surround the core and cover the inside of the core in the light pipe.
- the polymer optical waveguides may be arranged in a ribbon tape structure, or put together in an n by n array wherein n refers to an integer of 1 or greater.
- the polymer optical waveguides of this invention may be prepared by any process well known in the art for preparing optical fibers.
- the core and clad may be formed into a preform which is thereafter heated to a temperature at which the polymers may be redrawn, then the preform is drawn down to an appropriate size for the polymer optical waveguide.
- a fiber of the core may be extruded, and then the cladding may be coated on the core fiber and thereafter cured in place.
- cup coating techniques may generally be used in this approach, and any curing mechanism which adequately cures the cladding onto the core is suitable, for example, heat cure or ultraviolet cure.
- the optical fiber may be formed by a co-extrusion process wherein the core and the cladding are concurrently extruded to form the desired shape.
- a co-extrusion process the core material and cladding material are separately heated to a suitable temperature for extrusion, thereafter the polymers are extruded.
- the core material is fed into a pre-extrusion cylinder and simultaneously, the cladding material is fed into that cylinder about the outside of the core material, the materials are then passed through an orifice in a spinnerette into an air region wherein the fiber is cooled and drawn down to the desired fiber size.
- the extrusion temperature is dependent upon the particular core and cladding used and the temperature used must be suitable for both components.
- the temperature at which the fiber is co-extruded may be higher than the temperature at which a fiber is extruded wherein the cladding comprises other acrylics or a fluoropolymer.
- the core material and the cladding material are pre-heated separately to temperatures at which the polymers have a viscosity which is suitable for coextrusion. The temperatures of each pre-heating zone may be different.
- the cladding and core material are extruded at the same temperature, said temperature chosen to be compatible for the extrusion of both materials.
- Such extrusion temperatures are readily known, or ascertainable, by one skilled in the art.
- the core material is pre-heated to a temperature of between 400°F (205°C) to 545°F (285°C).
- the more preferred temperatures to which the core material is pre-heated is between 480 and 520°F (249°C to 271°C), even more preferably between 480 and 500°F (249°C to 260°C).
- the more preferred temperatures to which the core material is pre-heated is between 400 and 500°F (205°C to 260°C), even more preferably between 430 and 470°F (221°C to 243°C).
- the temperature to which the cladding material may be pre-heated is preferably between 410 and 510°F (210°C to 266°C), more preferably between 420 and 470°F (216°C to 244°C), and most preferably between 430 and 450°F (221°C to 233°C).
- the preferred preheat temperature is between 420 and 510°F (216°C to 266°C), even more preferably between 430 and 500°F (221°C to 260°C), and most preferably between 440°F and 490°F (227°C to 255°C).
- the temperature of the spinnerette at the point of extrusion is preferably between 410 and 540°F (210°C to 283°C).
- the core material is an aromatic ester carbonate or a blend of an aromatic ester carbonate and a polycarbonate wherein the total amount of ester linkages in the core is between 50 percent and 95 percent, with the remaining linkages being carbonate linkages, and the cladding is imidized acrylic material, an aromatic ester carbonate, or a blend of an aromatic ester carbonate with a polycarbonate or syndiotactic polymethylmethacrylate
- more preferred spinnerette temperatures are between 460°F (238°C) and 540°F (283°C), even more preferably between 470°F (244°C) and 520°F (271°C), and most preferably between 480°F (249°C) and 510°F (266°C).
- preferred spinnerette temperatures are between 410°F (210°C) and 480°F (249°C), more preferably between 420°F (216°C) and 460°F (238°C), and most preferably between 430°F (221°C) and 450°F (233°C).
- the preferred draw down ratio during formation of the optical fiber is between 5 and 75, more preferably between 10 and 50, and most preferably between 10 and 30.
- Draw down ratio as used herein means the ratio of the cross sectional area of the spinnerette orifice to the cross sectional area of the drawn fiber.
- the viscosity of the polymers under extrusion conditions should be within a range of between 10,000 (1,000 Pa ⁇ s) and 500,000 poise (50,000 Pa ⁇ s), more preferably between 20,000 (2,000 Pa ⁇ s) and 200,000 poise (20,000 Pa ⁇ s) and most preferably between 50,000 (5,000 Pa ⁇ s) and 100,000 poise (10,000 Pa ⁇ s).
- the difference in viscosity is less than 50,000 poise (5,000 Pa.s), more preferably 25,000 poise (2,500 Pa.s), with the core material having the higher viscosity.
- the optical fibers of this invention preferably have an attenuation of 8 or less dB per meter at 820 nanometers, more preferably less than 4 dB per meter and most preferably less than 3 dB per meter.
- the spinnerette temperature was about 490°F (255°C).
- An optical fiber was then melt spun through a 0.15 inch diameter die (3.81 millimeters) with a core pressure of 1500 psi (10,342 kPa) and a clad pressure of 500 psi (3,447 kPa).
- the fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller. The draw down ratio was about 25.
- the fiber diameter of the finished fiber was 0.75 mm, with a cladding thickness of 0.011 mm.
- the fiber take up during the process was 2.2 meters per minute.
- Fiber attenuation Is measured via the cut back technique, an experimental apparatus as described in Figure 1 comprising a helium neon laser 1 from which light is passed through a spacial filter 2 into a fiber coupler 3 coupling the light source with the fiber 4 with the other end of the fiber connected to a light detector 5.
- the optical power transmission in a given length of fiber is measured.
- An amount of fiber is then removed from the length and the power transmission is again measured.
- the optical loss of that cut back is given by the following equation.
- the length used in the equation is the length of the fiber cut off of the fiber tested. The cut back is repeated several times and an average is taken.
- the fibers were further measured for catastrophic loss temperature by the following procedure.
- a sample of plastic optical fiber four meters long is placed in chucks and both ends polished.
- the sample is loosely coiled and placed in an oven such that two meters are in the heated area and one meter on each end connects out to a light source and a photo detector, respectively.
- the output of the photo detector is displayed on a stripchart recorder.
- the source intensity and photo detector intensity are adjusted so as to give a nominal full deflection on the recorder under ambient conditions.
- the oven temperature is then increased at a rate of 1 or 2°C per minute.
- the intensity of light transmitted through the fiber as a function of the instantaneous temperatures plotted.
- a third test performed on these polymers was a water boil resistance. This method gives a rapid estimation of the polymer optical fiber's ability to resist moisture and humidity.
- the experimental procedure is the same as for the catastrophic loss measurement with the exception that the fiber is placed in a boiling water bath. The ability of the optical fiber to transmit light is measured over time while it is exposed. This sample is three meters long with one meter being immersed. The time period for the transmitted light intensity to be reduced to 80 percent of the original value is recorded.
- the clad side of the dual ram extruder was charged with a blend of an aromatic ester carbonate wherein the bisphenol portion is based on bisphenol A with an ester content of 75 mole percent and a bisphenol A polycarbonate to give a total ester linkage mole percentage of 25, and heated to 480°F (249°C) and transferred at 480°F (249°C).
- the spinnerette temperature was about 500°F (260°C).
- An optical fiber was then melt spun through a 0.15 inch diameter die (3.81 millimeters) with a core pressure of 1 150 psi ( 7929 kPa) and the clad pressure was 400 psi (2758 kPa).
- the fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller.
- the draw down ratio was 25.
- the fiber diameter of the finished fiber is 0.75 mm, with a cladding thickness of 0.009 mm.
- the fiber take-up during the process was 2.9 meters per minute.
- the fibers were tested in the same manner as described in Example 1 and the results of the testing are compiled in the table.
- Example 3 Polymer Optical Waveguide With Aromatic Ester Core and Blend of Aromatic Ester Carbonate and Polycarbonate Cladding
- the clad side of the dual ram extruder was charged with a blend of an aromatic ester carbonate wherein the bisphenol portion is based on bisphenol A with an ester content of 75 mole percent and a bisphenol A polycarbonate to give a total ester linkage mole percentage of 5, and heated to 450°F (233°C) and transferred at 460°F (238°C).
- the spinnerette temperature was about 510°F (266°C).
- An optical fiber was then melt spun through a 0.15 inch diameter die (3.81 millimeters) with a core pressure of 1500 psi (10,342 kPa) and a clad pressure of 300 pounds (2068 kPa). The fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller. The draw down ratio was 25.
- the fiber diameter of the finished fiber is 0.75 mm, with a cladding thickness of
- the fiber take-up during the process was 2.1 meters per minute.
- the fibers were tested in the same manner as described in Example 1 and the results of the testing are compiled in the table.
- Example 4 Polymer Optical Waveguide With Core of Aromatic Ester Carbonate Blended With Bisphenol A Polycarbonate and a Cladding of Polymethylmethacrylate
- the spinnerette temperature was about 510°F (266°C).
- An optical fiber was then melt spun through a 0.15 inch diameter die (3.81 milli-meters) with a core pressure of 1700 psi (11,721 kPa) and a clad pressure of 650 psi (4481 kPa).
- the fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller.
- the draw down ratio was about 25.
- the fiber diameter of the finished fiber is 0.75 mm, with a cladding thickness of 0.012 mm.
- the fiber take up during the process was 0.6 meters per minute.
- the fibers were tested in the same manner as described in
- Example 1 and the results of the testing are compiled in the table.
- Example 5 Polymer Optical Waveguide With Aromatic
- the clad side of the dual ram extruder was charged with a blend of an aromatic ester carbonate wherein the bisphenol portion is based on bisphenol A with an ester content of 75 mole percent with a bisphenol A polycarbonate to give a total ester linkage mole percentage of 5, and heated to 440°F (227°C) and transferred at 450°F (233°C).
- the spinnerette temperature was about 490°F (255°C).
- An optical fiber was then melt spun through a 0.15 inch diameter die (3.81 millimeters) with a core pressure of 1700 psi (11,721 kPa) and a clad pressure of 400 psi (2758 kPa).
- the fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller. The draw down ratio was about 25.
- the fiber diameter of the finished fiber is 0.75 mm, with a cladding thickness of 0.018 mm.
- the fiber take-up during the process was 1.3 meters per minute.
- the fibers were tested in the same manner as described in Example 1 and the results of the testing are compiled in the table.
- An optical fiber was then melt spun through a 0.15 inch diameter die (3-81 millimeters) with a core pressure of 1500 psi (10,342 kPa) and a clad pressure qf 1250 psi (8618 kPa).
- the fiber was spun into an air zone of ambient temperature, and drawn down by the use of a pinch wheel puller. The draw down ratio was about 25.
- the fiber diameter of the finished fiber is 0.75 mm, with a cladding thickness of 0.024 mm.
- the fiber take- up during the process was 2.7 meters per minute.
- the fibers were tested in the same manner as described in Example 1 and the results of the testing are compiled in the table.
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- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Un guide d'ondes optique en un matériau polymère comprend: (A) une âme en un carbonate d'ester aromatique ou en un mélange d'un carbonate d'ester aromatique avec un polycarbonate à base bisphénol; et (B) une gaine en polymère qui adhère à l'âme et présente un indice de réfraction inférieur à celui du carbonate d'ester aromatique ou du mélange du carbonate d'ester aromatique et du carbonate à base bisphénol. Ce guide d'ondes optique transmet la lumière à travers l'âme.An optical waveguide of a polymeric material comprises: (A) a core of an aromatic ester carbonate or a mixture of an aromatic ester carbonate with a bisphenol-based polycarbonate; and (B) a polymer sheath which adheres to the core and has a lower refractive index than that of the aromatic ester carbonate or of the mixture of the aromatic ester carbonate and the bisphenol-based carbonate. This optical waveguide transmits light through the soul.
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US6597387A | 1987-06-24 | 1987-06-24 | |
US65973 | 1987-06-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0319572A1 true EP0319572A1 (en) | 1989-06-14 |
EP0319572A4 EP0319572A4 (en) | 1990-11-28 |
Family
ID=22066418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19880906580 Withdrawn EP0319572A4 (en) | 1987-06-24 | 1988-06-23 | Aromatic ester carbonate polymer optical waveguides |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0319572A4 (en) |
JP (1) | JPH02501013A (en) |
KR (1) | KR890702055A (en) |
AU (1) | AU601072B2 (en) |
WO (1) | WO1988010438A1 (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0098578A1 (en) * | 1982-07-05 | 1984-01-18 | Mitsubishi Rayon Co., Ltd. | Plastic optical fibers |
US4547040A (en) * | 1983-06-21 | 1985-10-15 | Mitsubishi Rayon Co., Ltd. | Optical fiber assembly and process for preparing same |
US4575188A (en) * | 1982-04-12 | 1986-03-11 | Sumitomo Electric Industries, Ltd. | Heat resistant plastic optical fiber |
EP0191416A2 (en) * | 1985-02-06 | 1986-08-20 | Sumitomo Electric Industries Limited | Highly oriented resing-made reinforcing member and process for producing the same |
DE3537622A1 (en) * | 1985-10-23 | 1987-04-23 | Bayer Ag | MIXTURES OF AROMATIC POLYCARBONATES AND AROMATIC POLYESTER CARBONATES AND THEIR USE FOR THE PRODUCTION OF MOLDED BODIES, FILMS, FIBERS, FILAMENTS AND COATINGS |
JPS6321143A (en) * | 1986-07-15 | 1988-01-28 | 三菱レイヨン株式会社 | Composite molded form |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3999834A (en) * | 1973-08-14 | 1976-12-28 | Kanebo, Ltd. | Method for producing optical fibers and resulting fibers |
US4330662A (en) * | 1980-10-27 | 1982-05-18 | The Dow Chemical Company | Ordered copolyestercarbonate resins |
JPS60250310A (en) * | 1984-05-28 | 1985-12-11 | Daikin Ind Ltd | Clad material for optical fiber |
-
1988
- 1988-06-23 EP EP19880906580 patent/EP0319572A4/en not_active Withdrawn
- 1988-06-23 WO PCT/US1988/002128 patent/WO1988010438A1/en not_active Application Discontinuation
- 1988-06-23 AU AU21348/88A patent/AU601072B2/en not_active Ceased
- 1988-06-23 JP JP63506407A patent/JPH02501013A/en active Pending
- 1988-06-23 KR KR1019890700329A patent/KR890702055A/en not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4575188A (en) * | 1982-04-12 | 1986-03-11 | Sumitomo Electric Industries, Ltd. | Heat resistant plastic optical fiber |
EP0098578A1 (en) * | 1982-07-05 | 1984-01-18 | Mitsubishi Rayon Co., Ltd. | Plastic optical fibers |
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Non-Patent Citations (2)
Title |
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CHEMICAL PATENTS INDEX, BASIC ABSTRACTS JOURNALS, section A, week 8810, 4th May 1988, C88 - 030344, accession no. 88-067465/10, Derwent Publications Ltd, London, GB; & JP-A-63 021 143 (MITSUBISHI RAYON K.K.) 28-01-1988 * |
See also references of WO8810438A1 * |
Also Published As
Publication number | Publication date |
---|---|
JPH02501013A (en) | 1990-04-05 |
AU2134888A (en) | 1989-01-19 |
AU601072B2 (en) | 1990-08-30 |
WO1988010438A1 (en) | 1988-12-29 |
KR890702055A (en) | 1989-12-22 |
EP0319572A4 (en) | 1990-11-28 |
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