AU728110B2 - Thin carbon coating of optical waveguides - Google Patents
Thin carbon coating of optical waveguides Download PDFInfo
- Publication number
- AU728110B2 AU728110B2 AU78102/98A AU7810298A AU728110B2 AU 728110 B2 AU728110 B2 AU 728110B2 AU 78102/98 A AU78102/98 A AU 78102/98A AU 7810298 A AU7810298 A AU 7810298A AU 728110 B2 AU728110 B2 AU 728110B2
- Authority
- AU
- Australia
- Prior art keywords
- carbon
- coating
- optical waveguide
- waveguide fiber
- layer
- 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.)
- Ceased
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims description 66
- 229910052799 carbon Inorganic materials 0.000 title claims description 66
- 238000000576 coating method Methods 0.000 title claims description 63
- 239000011248 coating agent Substances 0.000 title claims description 59
- 230000003287 optical effect Effects 0.000 title claims description 20
- 239000000835 fiber Substances 0.000 claims description 49
- 229920000642 polymer Polymers 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000003086 colorant Substances 0.000 claims description 5
- 230000008859 change Effects 0.000 claims description 3
- 238000007654 immersion Methods 0.000 claims description 2
- 239000010410 layer Substances 0.000 claims 6
- XILIYVSXLSWUAI-UHFFFAOYSA-N 2-(diethylamino)ethyl n'-phenylcarbamimidothioate;dihydrobromide Chemical compound Br.Br.CCN(CC)CCSC(N)=NC1=CC=CC=C1 XILIYVSXLSWUAI-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000011247 coating layer Substances 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 17
- 230000007613 environmental effect Effects 0.000 description 7
- 230000008901 benefit Effects 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 230000032798 delamination Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
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
- G02B6/02—Optical fibres with cladding with or without a coating
- G02B6/02395—Glass optical fibre with a protective coating, e.g. two layer polymer coating deposited directly on a silica cladding surface during fibre manufacture
-
- 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
- G02B6/02—Optical fibres with cladding with or without a coating
- G02B6/02057—Optical fibres with cladding with or without a coating comprising gratings
- G02B6/02076—Refractive index modulation gratings, e.g. Bragg gratings
- G02B6/02114—Refractive index modulation gratings, e.g. Bragg gratings characterised by enhanced photosensitivity characteristics of the fibre, e.g. hydrogen loading, heat treatment
-
- 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
- G02B6/02—Optical fibres with cladding with or without a coating
- G02B6/02057—Optical fibres with cladding with or without a coating comprising gratings
- G02B6/02076—Refractive index modulation gratings, e.g. Bragg gratings
- G02B6/02123—Refractive index modulation gratings, e.g. Bragg gratings characterised by the method of manufacture of the grating
- G02B2006/02161—Grating written by radiation passing through the protective fibre coating
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
WO .98/59268 PCT/US98/11345
I
THIN CARBON COATING OF OPTICAL WAVEGUIDES Background of the Invention The invention is directed to a thin carbon coating on an optical wavegulde fiber. The coating acts to improve the waveguide fiber performance. More particularly, a thin carbon coating, formed on the clad glass layer of the waveguide fiber, has been found to improve dynamic fatigue performance of the waveguide fiber. In addition, the carbon coating markedly improves resistance to delamination between the polymeric coating and the waveguide fiber, under severe environmental conditions such as immersion in water.
The concept of coating optical waveguide fibers is known in the art.
Polymer coatings have been developed to protect the waveguide fiber from handling damage as well as to reduce the impact of bending on waveguide attenuation. Also, hermetic coatings have been developed to seal the waveguide fiber from OH- ions, which enable growth of waveguide surface flaws when the waveguide is under stress. A hermetic coating also is important in protecting the waveguide from corrosive materials, and gasses, particularly hydrogen, which can diffuse into the waveguide and cause increases in attenuation.
WO 98/59268 PCT/US98/11345 2 Of the several types-of coating material tested in the search for a hermetic coating, carbon has been found to be most compatible with the manufacture, packaging and use of a waveguide fiber.
The thickness of the carbon layer sufficient to provide hermeticity has been found to be in the range of 1000 oA or greater. In U.S. patent 4,964,694, Oohashi et al., carbon coating thickness of the range of 1000 to 6000 OA is taught (col. 3,11. 29 34). Thickness less than 1000 OA tend to allow pinhole formation in the coating. Thickness greater than 6000 OA tend to crack and peel from the waveguide surface. Hermeticity is also measured in terms of resistance to the passage of hydrogen through the coating. See, for example, U.S patent 5,000,541, DeMarcello et al., col. 4, 11. 19- 39. At col. 5, 11. 11-15, of '541 DeMarcello, a carbon layer of thickness of 1000 OA is noted as providing a barrier to the diffusion of hydrogen.
The manufacturing and cost penalties which arise from the incorporation of a carbon coating step into the waveguide fiber manufacturing process are: drawing speed is limited by the requirements of carbon coating thickness and integrity; an additional on line measurement of carbon coating thickness must be added to the draw feedback control loop; additional quality control testing for hermeticity must be done; and, the black color of the waveguide complicates the process of coloring the polymer layer to color code multiple fiber assemblies.
Summary of the Invention The invention overcomes the drawbacks of achieving hermeticity while maintaining some of the benefits thereof. Additional unexpected benefits also derive from the presence of the thin carbon coating.
Thus, a first aspect of the invention is an optical waveguide fiber coated with a carbon layer having a thickness no greater than about 100 It is contemplated that thickness no greater than 50 OA are sufficient. As carbon coating becomes thinner, one may expect the waveguide properties to -WO 98/59268 PCT/US98/11345 3 approach those of a non-carbon coated waveguide fiber. Some benefit in terms of carbon coated waveguide fiber performance may be expected at thickness about 10 pm. The thin carbon layer is distinguished from a hermetic carbon coating by its permeability to fluids, such as hydrogen. However, the dynamic fatigue constant, which is about 20 for a silica clad waveguide, is greater than about 25 in the case of a waveguide having a thin carbon layer. This increase is quite significant in light of the fact that the fatigue constant appears as an exponent in the equation predictive of time to failure.
In addition to the characterization of the thin carbon layer by its thickness, the layer may also be characterized by its resistance per unit length, which is no greater than about 4 Mega-ohms/cm (MQ/cm). The thin layer of carbon is bonded to the waveguide clad glass layer. The layer is colored a light gray.
A second aspect of the invention is the surprising discovery that the thin carbon layer acts to essentially prevent delamination of the polymer coating. The integrity of the waveguide fiber having a protective polymer coating is such that substantially no attenuation increase was induced by immersing the carbon and polymer coated waveguide in water for extended time periods. The standard environmental tests call for room temperature water soak and hot water soak, about 65 0C, for 30 days. The tests on the novel carbon coated waveguide fiber were extended to 128 days, in both room temperature and hot water, and still substantially no induced attenuation was observed.
An additional benefit of the coating results from its light gray color which allows, in contrast to the black hermetic coating, the waveguide fiber to be color coded using methods and pigments known in the art. The colors successfully applied and tested were yellow, white, red, and green. These colors are believed to be the most difficult to apply and the most likely to change in environmental testing.
-WO.98/59268 ~WO9859268PCTIUS98/1 1345 4 Brief Summary of the Drawings FIG. 1 is an end view of an optical waveguide fiber having a thin carbon coating and a polymer coating.
FIG. 2 is a Weibull strength chart showing failure probability vs. applied stress.
FIG. 3 is a chart of attenuation vs. time for a waveguide in an environmental test.
Detailed Description of the Invention The optical waveguide fiber having the novel thin carbon coating is characterized by: a dynamic fatigue constant greater than about superior polymer coating adhesion in severe environments; and, ease of coloring similar to that of a polymer coated waveguide having no carbon layer. Thus, a strength benefit of a carbon coated waveguide is realized, while essentially none of the drawbacks associated with a hermetic coating need be dealt with. In addition to the ease of coloring, it is believed the thin carbon coat may be applied at higher draw speeds than that of a hermetic coating process. No additional on line measurements coupled to the draw control loop are required and quality control can be maintained by making a statistically significant number of off line measurements of coating electrical resistance. These statements are based upon the results, discussed below, which show that resistance per unit length of the order of mega-ohms provide a suitable thin coating. In sharp contrast, the resistance requirement for a hermetic carbon coating, a coating having a thickness no less than about 500 is in the kilo-ohm range, three orders of magnitude lower.
The end view illustration of the novel waveguide is shown in FIG. 1.
The clad glass layer 2 is surrounded by and adhered to thin carbon layer 4.
The outer layer 6 represents the protective polymer coating, which may comprise one or more layers. Note that the carbon layer is formed directly onto the glass surface of the waveguide fiber.
WO 98/59268 PCT/US98/11345 A method of forming the coating comprises pyrolytic deposition of carbon onto the waveguide fiber as the fiber emerges from the hot zone of the draw furnace. The fiber passes from the hot zone into a controlled environment chamber where a carbon containing compound reacts to produce a carbon layer on the waveguide surface. The reaction may be driven by the heat from the waveguide fiber. A process suitable for applying a hermetic coating or the thin carbon coating of this application is found in U.S. patent 5,346,520, Meabon, et al ('520 patent).
Because the concentration of the carbon containing compound in the reactor is low in the thin coating process, the pyrolytic reaction tended to be somewhat unstable. The pyrolytic reaction was stabilized by introducing a relatively inert gas into the flow. A gas such as argon was used. Depending upon the thickness of the carbon coated layer, the flow rate of the argon was in the range of 0 to 75% by volume of the total flow of gas into the reactor vessel.
Example Strength Testing of Carbon Coated Waveguides A waveguide fibers was prepared having a thin carbon coating on the clad glass surface. A polymer coating was applied over the carbon coating.
The waveguide was strength tested to determine a Weibull strength distribution and a dynamic fatigue constant.
The Weibull plots shown in FIG. 2 show the failure probability of the fiber versus applied stress. The steep slope, straight line appearance of the plots is markedly similar to those characteristic of hermetic coated waveguides.
The data was generated by applying linear tension to break the fiber in 20 meter gauge lengths. The environment was controlled to a temperature of OC and a relative humidity of 100%. Curve 10 is the failure probability vs.
stress using a strain rate of 0.004 %/min. Curve 8 represents a strain rate of %/min. The shift to the right of the higher strain rate curve is expected because the higher rate does not allow time for certain of the waveguide surface flaws to grow to failure. In effect, the higher strain rate acts upon a smaller distribution of flaws, i.e. faster growing flaws.
WO 98/59268 PCT/US98/11345 6 The dynamic fatigue constant was determined by fitting a line on a chart of break strength vs. stress rate. Multiple readings of strength at failure were taken at each of the two stress rates and nd, the dynamic fatigue constant, was found by fitting a line to the data. The method is known in the art and detailed in Fiber Optic Test Procedure (FOTP) 76, published by a U.S. standards group.
Table 1 Sample Gauge Humidity n Resistance A 20 100 RH 27.5 3.8 MD/cm Sample Gauge Humidity nd Resistance A 20 100 RH 27.5 3.8 MD/cm A 0.5 50 %RH 23.3 3.8 MD/cm A 0.5 50 %RH 26.7 3.8 MD/cm A 0.
5 50 RH 34.0 3.8 MD/cm The 20 meter gauge test is more reliable than the 0.5 meter gauge test.
It is not unusual for the shorter gauge test to yield a lower value of ni.
However, the data point which gives an nd of 23.3 may indicate that the carbon coating resistance of about 4 M /cm is near the limit of how thin the carbon coating may be. To test this hypothesis, the testing of three additional fibers was carried out at the shorter gauge length. The data is significant and does show the carbon coating is effective to increase nd to about 25 as compared to a waveguide having no carbon coating for which nd is typically about 20. By comparison, a thicker, hermetic carbon coating provides an n value of 200 or greater.
SUBSTITUTE SHEET (RULE 26) -WO.98/59268 PCT/US98/11345 7 Comparative Example Additional Strength Testing A second waveguide fiber having a thin carbon layer on the clad glass surface was prepared. In this case the electrical resistance per unit length was 1.28 MO/cm, about a factor of three lower than the previous example, indicative of a thicker carbon layer. The data is given in Table 2.
Table 2 Sample Gauge Humidity nd Resistan B 0.5 50% RH 26.7 1.28 Mz, The data again shows the effectiveness of the thin carbon layer in greatly improving the fatigue constant. The two data sets taken together suggest that a target thickness of about 4 MO/cm may be appropriate.
Turning now to the effect of the carbon layer on polymer coating adhesion, it is noted that both of the waveguide fibers described in the examples performed well. Table 3 shows the test waveguides had essentially no degradation in coating adhesion or waveguide function under severe environmental testing.
SUBSTITUTE SHEET (RULE 26) -WO.98/59268 PCT/US98/11345 Table 3 Sample Environ't Time Delamin'n DA 1310 DA 1550 A 23 0 C Water 17 days no A 31 days no A 128 days no 0.01 dB/km 0.01 dB/km A 65 0 C Water 17 no A 31 no
IE
A 1" 28 no 0.04 dB/km 0.03 dB/km B 23*C Water 17 no B 31 no B 128 no 0.03 dB/km 0.01 dB/km B 65°C Water 17 no B 30 no B 128 no 0.03 dB/km 0.01 dB/km The absence of delamination of the coating from the carbon coated waveguide is unusual. More unusual is the very small change in attenuation of the waveguide in these severe environments. The results of the testing of the B samples are of particular import. The B samples had no adhesion promoter, so that the lack of delamination is quite unusual and unexpected. Such a coating applied to a silica surface would have delaminated very quickly, in no more than a few hours. Coating delamination causes strength degradation as well as increased attenuation. A typical environmental testing data set is shown charted in FIG. 3. The chart is a plot of attenuation vs. time for waveguide fiber A immersed in 65 OC water. Curve 12 shows the essentially continuous data readout of waveguide A attenuation at 1310 nm over the 128 SUBSTITUTE SHEET (RULE 26) -WO.98/59268 PCT/US98/11345 9 day time period. Curve 14 is a plot of 1550 nm attenuation for waveguide A.
The small attenuation increase is, for essentially all applications, not sufficient to degrade performance of a system comprised of this waveguide fiber.
The required thickness of the novel carbon coating may be determined by: direct measurement made on a waveguide fiber end; measurement of electrical resistance or another electrical property related to carbon thickness; color of the carbon coated waveguide.
This last characteristic affords another benefit of the novel thin carbon coating. Hermetic coated fiber requires a thicker carbon layer and thus appears black. The polymer coating may be somewhat transparent so that a color added to the polymer coat may be changed in appearance by the underlying black layer. In point of fact, considerable difficulty has been encountered in manufacture of yellow, white, green, and red polymer coated hermetic fibers because of the black layer.
The light gray color of the carbon coated waveguide fiber disclosed herein does not interfere with the color added or applied to the polymer.
Furthermore, the colors remain within specification, as determined by a standard Muncell color chart, when subjected to standard environmental testing.
Although particular embodiments of the invention have herein been disclosed and described, the invention is nonetheless limited only by the following claims.
Claims (6)
1. A coated optical waveguide fiber, comprising: an optical waveguide fiber having an outer surface, wherein said outer surface has a coating comprising carbon, having a thickness no greater than about 100 oA, and, wherein the optical waveguide fiber has at least one polymer coating surrounding and in contact with said carbon layer.
2. The coated optical waveguide fiber of claim 1, wherein said layer comprising carbon has a thickness no greater than about 50 OA.
3. The coated optical waveguide fiber of claim 1 wherein the dynamic fatigue constant
4. The coated optical waveguide fiber of claim 1 wherein said carbon coating has an electrical resistance per centimeter of waveguide length no greater than about 4 MQ/cm. The coated optical waveguide fiber of claim 4 wherein the electrical resistance per cm of said carbon coating is no greater than about 2.5 MO/cm.
6. A coated optical waveguide fiber, comprising: an optical waveguide fiber having an outer surface, wherein said outer surface has a first coating comprising a layer of carbon, having a thickness no greater than about 100 OA, and at least one additional coating layer comprising a polymer, surrounding and in contact with said thin carbon layer, and, ANMMOE S'-IW FILE No.4i ?2 05/10 '99 15:04 ID:CORNING PATENT DEPT FrAX:6079742407
9-q Wu POT/US 98/11 4..PEANUS 1( MAY wherein said layer comprising carbon remains in contact with said surrounding polymer layer when immersed for at least 30 days in water, having a temperature in the range of about 20 to 70 00. PAGE 345 1999 AMENDD SKST WO-98/59268 PCT/US98/11345 11 7. The coated optical waveguide fiber of claim 6 wherein the change in optical attenuation of the waveguide during and after water immersion is no greater than about 0.04 dB/km at 1310 nm and about 0.03 dB/km at 1550 nm. 8. The optical waveguide fiber of claim 6 further comprising coloring agents in said polymer coating. 9. The optical waveguide of claim 8 wherein the color agents produce waveguide fibers having one of the colors yellow, white, green, and red.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5055197P | 1997-06-23 | 1997-06-23 | |
| US60/050551 | 1997-06-23 | ||
| PCT/US1998/011345 WO1998059268A1 (en) | 1997-06-23 | 1998-06-03 | Thin carbon coating of optical waveguides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU7810298A AU7810298A (en) | 1999-01-04 |
| AU728110B2 true AU728110B2 (en) | 2001-01-04 |
Family
ID=21965908
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU78102/98A Ceased AU728110B2 (en) | 1997-06-23 | 1998-06-03 | Thin carbon coating of optical waveguides |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1015919A4 (en) |
| JP (1) | JP2002508856A (en) |
| KR (1) | KR20010014101A (en) |
| CN (1) | CN1260881A (en) |
| AU (1) | AU728110B2 (en) |
| BR (1) | BR9809521A (en) |
| CA (1) | CA2291143A1 (en) |
| ID (1) | ID25603A (en) |
| WO (1) | WO1998059268A1 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6895156B2 (en) | 2001-10-09 | 2005-05-17 | 3M Innovative Properties Company | Small diameter, high strength optical fiber |
| US6944377B2 (en) | 2002-03-15 | 2005-09-13 | Hitachi Maxell, Ltd. | Optical communication device and laminated optical communication module |
| EP2138471A1 (en) * | 2008-06-25 | 2009-12-30 | Acreo AB | Atomic layer deposition of hydrogen barrier coatings on optical fibers |
| CN103777272B (en) * | 2014-01-15 | 2017-01-11 | 烽火通信科技股份有限公司 | Long-service-life optical fiber applicable to high-stress environment |
| CN104901428B (en) * | 2015-06-12 | 2017-07-28 | 长沙景嘉微电子股份有限公司 | A kind of S-shaped charge-discharge circuit |
| KR101959496B1 (en) | 2018-11-27 | 2019-07-02 | (주)지엠디텔레콤 | Satellite waveguide and manufacturing method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4183621A (en) * | 1977-12-29 | 1980-01-15 | International Telephone And Telegraph Corporation | Water resistant high strength fibers |
| US4964694A (en) * | 1988-07-26 | 1990-10-23 | Fujikura Ltd. | Optical fiber and apparatus for producing same |
| US5717809A (en) * | 1994-08-25 | 1998-02-10 | Alcatel Fibres Optiques | Optical fiber coated with an amorphous boron protective layer, and a method of depositing such a layer |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8912470D0 (en) * | 1989-05-31 | 1989-07-19 | Stc Plc | Carbon coating of optical fibres |
| JP2975642B2 (en) * | 1989-06-13 | 1999-11-10 | 住友電気工業株式会社 | Hermetic coated fiber and manufacturing method thereof |
-
1998
- 1998-06-03 EP EP98926208A patent/EP1015919A4/en not_active Withdrawn
- 1998-06-03 ID IDW20000101A patent/ID25603A/en unknown
- 1998-06-03 JP JP50447199A patent/JP2002508856A/en active Pending
- 1998-06-03 CA CA002291143A patent/CA2291143A1/en not_active Abandoned
- 1998-06-03 WO PCT/US1998/011345 patent/WO1998059268A1/en not_active Ceased
- 1998-06-03 AU AU78102/98A patent/AU728110B2/en not_active Ceased
- 1998-06-03 KR KR19997012148A patent/KR20010014101A/en not_active Withdrawn
- 1998-06-03 CN CN 98806163 patent/CN1260881A/en active Pending
- 1998-06-03 BR BR9809521-8A patent/BR9809521A/en not_active IP Right Cessation
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4183621A (en) * | 1977-12-29 | 1980-01-15 | International Telephone And Telegraph Corporation | Water resistant high strength fibers |
| US4964694A (en) * | 1988-07-26 | 1990-10-23 | Fujikura Ltd. | Optical fiber and apparatus for producing same |
| US5717809A (en) * | 1994-08-25 | 1998-02-10 | Alcatel Fibres Optiques | Optical fiber coated with an amorphous boron protective layer, and a method of depositing such a layer |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1260881A (en) | 2000-07-19 |
| BR9809521A (en) | 2000-06-20 |
| ID25603A (en) | 2000-10-19 |
| CA2291143A1 (en) | 1998-12-30 |
| JP2002508856A (en) | 2002-03-19 |
| EP1015919A1 (en) | 2000-07-05 |
| WO1998059268A1 (en) | 1998-12-30 |
| AU7810298A (en) | 1999-01-04 |
| KR20010014101A (en) | 2001-02-26 |
| EP1015919A4 (en) | 2003-02-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |