GB2118165A - Improved manufacture of optical fibers - Google Patents
Improved manufacture of optical fibers Download PDFInfo
- Publication number
- GB2118165A GB2118165A GB08309433A GB8309433A GB2118165A GB 2118165 A GB2118165 A GB 2118165A GB 08309433 A GB08309433 A GB 08309433A GB 8309433 A GB8309433 A GB 8309433A GB 2118165 A GB2118165 A GB 2118165A
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- Prior art keywords
- tube
- velocity
- function
- deposition
- heat source
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- 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.)
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- 239000013307 optical fiber Substances 0.000 title claims abstract description 26
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 238000000151 deposition Methods 0.000 claims abstract description 54
- 230000008021 deposition Effects 0.000 claims abstract description 49
- 239000000463 material Substances 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 34
- 239000000376 reactant Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 2
- 230000003247 decreasing effect Effects 0.000 claims 1
- 239000002243 precursor Substances 0.000 abstract description 8
- 239000011521 glass Substances 0.000 abstract description 6
- 238000005229 chemical vapour deposition Methods 0.000 abstract description 3
- 239000007789 gas Substances 0.000 description 8
- 238000005253 cladding Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000002019 doping agent Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 2
- 238000005137 deposition process Methods 0.000 description 2
- 238000005315 distribution function Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 244000027321 Lychnis chalcedonica Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 235000017899 Spathodea campanulata Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 239000012792 core layer Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 238000007496 glass forming Methods 0.000 description 1
- 238000012804 iterative process Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- CMDGQTVYVAKDNA-UHFFFAOYSA-N propane-1,2,3-triol;hydrate Chemical compound O.OCC(O)CO CMDGQTVYVAKDNA-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
- C03B37/01—Manufacture of glass fibres or filaments
- C03B37/012—Manufacture of preforms for drawing fibres or filaments
- C03B37/014—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD]
- C03B37/018—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD] by glass deposition on a glass substrate, e.g. by inside-, modified-, plasma-, or plasma modified- chemical vapour deposition [ICVD, MCVD, PCVD, PMCVD], i.e. by thin layer coating on the inside or outside of a glass tube or on a glass rod
- C03B37/01807—Reactant delivery systems, e.g. reactant deposition burners
- C03B37/01815—Reactant deposition burners or deposition heating means
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Manufacture, Treatment Of Glass Fibers (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
Abstract
Improved method of making optical fibers utilizing a technique for minimizing taper, including entrance taper, in an optical fiber preform made by the deposition of reacted glass precursor material on the inside of a tube. In one embodiment, a torch (or other heat source) deposition function is determined, which relates the amount of deposited material as a function of distance from the torch or other heat source. A velocity profile for the moving heat zone can then be determined that minimizes taper. For example, in a single mode optical fiber preform made by the modified chemical vapor deposition technique, a reduction in entrance taper in a 90 cm long preform of from about 30 cm (31) using a linear velocity profile to about 10 cm (32) with a profile determined according to the inventive technique is achieved.
Description
SPECIFICATION
Improved manufacture of optical fibers
This invention relates to an improved method of making optical fibers. In particular, it relates to a method of reducing the taper in optical fiber preforms.
In the production of optical fibers, a preform is initially made, from which an optical fiber is subsequently drawn. Some techniques for making a preform include the step of depositing silica, possibly including dopants, onto the inside surface of a tube. One commerically successful technique is described in U.S. Patent No.
4,21 7,027, coassigned with the present invention, which describes the modified chemical vapor deposition (MCVD) technique. In the MCVD technique, glass precursor material, typically including SiCI4 and an oxidizing medium, are flowed through a rotating tube. A moving external heat source heats the rotating tube while traversing the length of the tube. The resulting moving hot zone in the tube causes oxidation of the glass-forming precursors, and deposition of reacted material upon the inside of the tube. The deposition occurs downstream from the moving heat source due to the flowing gaseous precursors inside the tube. Then, the moving heat source heats and consolidates the previously deposited material to produce a glass layer.
However, because the silica material tends to deposite downstream from the heat source, there tends to be less material deposited where the reactants enter the tube (referred to as the entrance of the tube). The material slowly increase in thickness at downstream portions of the tubes. This is referred to as the "taper" of the deposit, and as the effect is more pronounced near the entrance of the tube, the term "entrance taper" is also frequently used in the art. The tube and deposited material is then collapsed, and an optical fiber drawn from the preform.
An optical fiber typically comprises a core surrounded by a cladding, with one or both being deposited inside the tube by the MCVD or other process. A taper will produce an axially nonuniform cross-sectional area of the core after a fiber is drawn from the preform. This nonuniformity can, in some cases, produce a degradation in the transmission qualities of the fiber. Therefore, the entrance taper portion of the preform, which typically comprises about 10 to 20 percent of the length of the preform, is not used in making an optical fiber. Clearly, this is not a desirable situation, and steps have been proposed for reducing the entry taper. One proposal for reducing the taper has been to modify the flow of reactants into the tube as the torch moves along the length of the tube.
However, this typically is difficult to control and can result in unintended shifts in the composition of the deposited material, particularly when dopants, for example germanium, phosphorus, boron, fluorine, etc., are included in the gaseous reactants. Other techniques have kept the flow rate of gases constant but have varied the velocity of the torch as it traverses the tube. Slowing the velocity of the torch will result in relatively more material being deposited in the vicinity of the torch. Various "ramping" profiles, by which the torch velocity is slowed down at the entrance of the tube, have been proposed. Linear ramping can reduce the taper to some extent, but the entry taper still remains larger than is desirable. Step functions and exponential functions have been proposed.Improved methods of reducing the taper, including the entry taper, in an optical fiber preform are desirable.
According to the present invention there is provided a method of making an optical fiber by steps comprising introducing reactant material into the entrance of a tube, reacting said material by means of a heat source movable relative to the tube, and depositing reacted material on the inside of said tube, with said heat source traversing substantially the length of said tube, collapsing said tube to form a solid rod, and drawing an optical fiber from the rod, wherein the velocity of said heat source axially along the tube is a function of the position of said heat source along said tube so that the equation
is substantially constant over ai maximum length of said tube, where D(Z) is the total deposition thickness of said reacted material at a distance Z along said tube, d(ZZt) is the heat zone deposition function, and V(Zt) is the velocity of said heat source along said tube.
We have invented a methods reducing the taper in an optical fiber preform. We provide for an initial heat source velocity that is relatively low near the entrance of the tube, which then increases as the heat source proceeds along the tube, and then decreases for a portion of the traverse of the tube. The velocity then either remains constant, or increases as the heat source continues toward the end of the tube. The proper velocity profile can be determined by a heat zone deposition function, which relates the rate at which a material is deposited along a length of the tube in the vicinity of a torch or other heat source in relation to the position of the heat source. Once the heat zone deposition function is at least approximately determined, it is used to calculate a heat source velocity that reduces the taper.The deposition thickness is then experimentally determined using this heat source velocity function. If the taper is still excessive, an error function is calculated which is then used to improve the heat source velocity function. By one or more successive approximations, a heat source velocity profile is obtained which minimizes taper, including entrance taper, in an optical fiber preform.
Brief description of the drawings
Fig. 1 shows a typical preform deposition technique;
Fig. 2 shows a typical heat zone deposition function for a torch;
Fig. 3 and 4 show torch velocity, and resulting deposition depth as a function of position along a tube, using a constant velocity and also using a profile of the present technique;
Fig. 5 shows a typical heat zone deposition function for a plasma-assisted deposition process.
Detailed description
The following detailed description refers to a method of making an optical fiber preform wherein the torch (or other heat source traversing the length of a preform tube) velocity is varied to achieve a more constant deposited layer thickness. Referring to Fig. 1, a stream of reactant gases enters a tube, typically made of glass, that serves as the substrate for the deposition of optical fiber material. This tube is frequently referred to as the "support tube" in the art.
Normally, both cladding layers and core layers are deposited on the inside of the tube. However, in some techniques, the tube itself serves as a cladding, with the deposited material becoming substantially only the core of a resulting optical fiber. The difference between the cladding and the core is normally one of dopants included in the reactant gases used for producing the inner core that raise the index of refraction of the deposited glass. Alternately, or additionally, dopants can be included in the cladding portion that lower the index of refraction of the deposited glass, as compared to pure silica.
Referring to Fig. 1, precursor gases (10) are flowed into a rotating tube (12). A torch (11) is used for reacting the gases, causing subsequent deposition on the inside of the tube. The position of the centre of the flame of the torch is located a distance Zt from the entrance of the tube. The highest deposition rate for the precursor materials will be at distance Zmax along the tube downstream from the torch. The distribution of deposited material that forms due to the torchinduced reaction is referred to herein as the "torch deposition function" and is illustrated qualitatively in Fig. 2. Notice that the distribution of material falls off more slowly to the right (downstream) side of Zmax, due to the flow of reactant gases in the direction shown in Fig. 1.
While the deposition is shown being entirely downstream of Zt (i.e., where ZZt > O) in Fig. 2.
deposition can also occur upstream. This is because Zt is defined as the distance to a fixed point in the heat zone, but a broad heat zone (for example) can deposit some material upstream of the defined point.
In the present invention, the torch deposition function is first determined, being expressed as a function of the form: d(ZZt) (1) where d is the local deposition rate at position Z when the torch is at Zt. (All positions are measured from the entrance end of the tube, where the reactant gases are introduced into the tube.) The deposition rate can conveniently be expressed in units of grams per minute per unit of tube length. When the torch deposition function is determined, it is inserted in Equation (2):
D(Z), the total deposition function, gives the total amount of deposit at axial position Z, where V is the torch velocity as a function of torch position.
The torch deposition function can be determined in a variety of ways. One method is to simply flow precursor gases through the tube and hold the torch at a given position for a period of time. Then, the amount of deposited material in the vicinity of the torch is measured and the deposition function determined directly. That method suffers from the disadvantage that because the torch is held stationary, the temperature profile on the tube will be determined solely by the stationary torch. In practice, in producing an MCVD preform, the torch is moving along the tube so that some portions of the tube have been heated more recently than others due to the torch traversing the length of the tube and returning. Therefore, the actual tube wall temperature profile will not be as simple as that indicated by a stationary torch.
The presently preferred method for determining the torch deposition function is to first deposit a quantity of material in the tube by traversing the length of the tube a number of times with the torch, typically at a constant velocity. To measure the thickness of deposited material along the tube, it is convenient to immerse the preform into an index-matching fluid, illuminate the preform from behind, and scan across the diameter of the preform with a microscope. The microscope reveals the precise point of interface between the deposited material and the fluid inside the preform, and hence the thickness of the deposit. A scan at least every 2 cm in the entrance region, and about every 5 cm along the rest of the length of the preform, has been found to yield adequate accuracy. For the index-matching fluid, a glycerine-water mixture is satisfactory. This measurement gives D(Z), the total deposition function, for the velocity profile used. This measured value of D(Z), which includes an entrance taper, can then be substituted in
Equation (2). Then, d(ZZt) is solved in
Equation (2), with V(Zt) being known. Then, d(ZZt) is used to optimize the velocity profile for reduced taper. This is accomplished by setting the total deposition function D equal to a constant, referred to as D* and using the function d(ZZt) determined above; see Equation (3).
Then, the velocity V is solved for, in Equation (3), with the resulting velocity being referred to as V1.
In the next step, a preform is then made using the velocity V1. Then, the resulting thickness of the deposited material is measured (as before) and is referred to as DE. An error function is defined, referred to as D**; see Equation (4).
Note that D** D* over most of the length of the tube. From equation (4) is calculated a new velocity correction factor, referred to as V'1. A preform is then fabricated using a new corrected velocity, as given in Equation (5).
1 1 1 ~=~~ + (5)
V Vj V"
This process is repeated as many times as is necessary to achieve a velocity function that produces the uniformity of deposition depth to within a desired value. Usually, the error function decreases rapidly, and only 1 to 3 iterations are typically required.
The above-noted technique was used to reduce the taper in an optical fiber preform, as further discussed in the following Example.
Example
An optical fiber preform was made using a support tube having an inside diameter of 1 9 mm, and outside diameter of 25 mm, and a length of about 90 cm. Flowing through this tube was SiCI4 at 12 grams/minute, 02 at 2 liters/minute, He at 6 liters/minute, and in addition, small amounts of Six, and POCI3 were added for achieving a desired refractive index. The preform was made using a total of 1 5 passes of the torch to deposit material on the inside of the tube at a deposition rate of 2.3 grams/minute. Initially, a constant torch velocity was used, as shown at 41 in Fig. 4. This produced a tapered deposit radius, as shown at 31 in Fig. 3. Next, the iteration procedure discussed above was used to optimize the torch velocity.Two iterations were performed, as indicated by Equations (2)-(5) above, with corresponding measurements being made of the deposition thickness for each iteration in order to construct the next correction factor for the velocity. The resulting torch velocity is shown as line 42 in Fig. 4, which produced a resulting profile shown as line 32 in Fig. 3. It can be seen that a substantial reduction in the taper, and especially a reduction in that portion near the entrance of the tube, has been achieved; the entrance taper length was only about 10 cm.
Further iterations of the above-noted technique can be used to further reduce the taper
Referring to Fig. 4, there are several features of significance in the velocity profile 42. Near the entrance of the tube, the torch initially starts out at a relatively low velocity in portion 43. In some cases, this initial velocity may be approximately zero. In a second region 44 of the curve, the velocity initially increases over that of region 43, and then decreases. This is a significant departure from prior art velocity profiles, which typically called for an increase in the torch velocity as a function of distance. Next, the torch enters region 45 wherein the velocity again increases. In some cases, the velocity increase may be small; that is, approximately zero in region 45.If only an optimized linearly increasing torch velocity had been used, we estimate the entry taper in the above Example would be about 30 cm.
The above process has been described mainly in terms of a single torch which produces a single heat zone. However, other preform fabrication processes are also possible. For example, a plasma process using a tandem heat zone is described in U.S. patent application Serial No.
143,834, filed April 25, 1 980, and coassigned with the present invention. In that technique, species of which may or may not be an MCVD process, a tandem heat zone is provided with zone I being produced by a plasma and zone II typically, although not necessarily, produced by a torch for consolidation of particles that are produced. For a tandem heat zone, a deposition function such as shown in Fig. 5 can result, with other shapes being possible. In that Figure, Zmax is the position of maximum deposition due to the torch, and Zmax2 is that due to the plasma fire ball.
In addition, water cooling of a heat zone can be provided, such as shown in U.S. Patent No.
4,302,230, coassigned with the present invention. The use of water cooling can affect the torch deposition function. However, a torch deposition function can be determined whatever the nature of the heat source applied. Note that the term "torch" is used illustrative in this context, and the heat source may be by other means. Thus, the term "heat zone distribution function" generally describes the distribution of particulate matter due to reactions by precursor materials in a heat zone, whether produced by a torch or otherwise.
While the heat zone distribution function has been determined above by using an iterative technique based upon the deposition depth of a trial preform, and with the further possibility of determining the deposition function directly by the use of a stationary torch, another possibility is to determine the deposition rate based upon the temperature of the wall of the tube and the temperature at which the reaction occurs. A thermophoretic model can then be used to estimate the deposition of particles along the tube; see, for example, "Thermophoretic
Deposition of Small Particles in the Modified
Chemical Vapor Deposition (MCVD) Process," by
K. L. Walker et al, in the Journal of the American
Ceramic Society, Vol. 63, pages 552-558 (1980). See also "Thermophoretic Deposition of
Small Particles in LaminarTube Flow," by K. L.
Walker et al, in the Journal of Colloid lntefface Science, Vol. 69, pages 138-147 (1979). Other methods of modeling a deposition process, and thereby calculating the heat zone deposition function, may be used as desired by persons of skill in the art.
It is furthermore apparent that based upon the above observation, that a decrease in heat zone velocity, following a rapid increase in velocity, is typically required to obtain a reduction in taper, it is apparent that an empirical technique can be utilized to directly determine the appropriate torch velocity without the use of the heat zone deposition function. However, the use of the heat zone deposition function has been found to significantly aid in determining the appropriate heat zone velocity according to the iterative process noted above.
All such variations and deviations through which the present invention has advanced the art are considered to be within the spirit and scope of the present invention.
Claims (6)
1. A method of making an optical fiber by steps comprising introducing reactant material into the entrance of a tube, reacting said material by
means of a heat source movable relative to the tube, and depositing reacted material on
the inside of said tube, with said heat source traversing substantially the length of said tube, collapsing said tube to form a solid rod, and drawing an optical fiber from the rod, wherein the velocity of said heat source axially along the tube is a function of the position of said heat source along said tube so that the equation
is substantially constant over a maximum length of said tube, where D(Z) is the total deposition thickness of said reacted material at a distance Z along said tube d(ZZt) is the heat zone deposition function, and V(Zt) is the velocity of said heat source along said tube.
2. The method according to claim 2 wherein the heat zone deposition function d(ZZt) is determined by steps comprising depositing an amount of material on the inside of a tube at a given velocity and thereafter determining the amount of material so deposited as a function of the position along said tube.
3. The method according to claim 2, whereby an error function is defined as the difference between a calculated value of D(Z) and a value determined by measuring the deposition thickness at points axially along the tube, and thereafter calculating a new velocity function
V(Zt) that reduces the differences in deposition thickness axially along the tube.
4. A method according to claim 1,2 or 3, wherein the veloctiy of the heat source comprises a first velocity region in the vicinity of the entrance end of the tube into which reactants are introduced, a second velocity region downstream of said first velocity region that is initially at a higher velocity than any velocity attained in said first velocity region, and with the velocity thereafter decreasing in said second velocity region and a third velocity region downstream of said second velocity region, in which third region the velocity is nondecreasing, whereby the length of the entrance taper in said tube, defined as the region in which the thickness of the deposited material in the vicinity of the entrance of the tube is substantially less than the thickness of the material in downstream portions of the tube, is substantially reduced as compared to the entrance taper in a tube made at a constant torch velocity.
5. A method of making an optical fibre, substantially as hereinbefore described with reference to Figs. 3, 4 and 5 of the accompanying drawings.
6. An optical fiber made according to the method of any one of Claims 1 to 5.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36756182A | 1982-04-12 | 1982-04-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB2118165A true GB2118165A (en) | 1983-10-26 |
Family
ID=23447680
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB08309433A Withdrawn GB2118165A (en) | 1982-04-12 | 1983-04-07 | Improved manufacture of optical fibers |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0105327A4 (en) |
| JP (1) | JPS59500512A (en) |
| AU (1) | AU1477783A (en) |
| CA (1) | CA1188102A (en) |
| GB (1) | GB2118165A (en) |
| WO (1) | WO1983003600A1 (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0209945A1 (en) * | 1985-07-20 | 1987-01-28 | Philips Patentverwaltung GmbH | Method for making optical fibres |
| US4741747A (en) * | 1984-12-12 | 1988-05-03 | U.S. Philips Corporation | Method of fabricating optical fibers |
| US5188648A (en) * | 1985-07-20 | 1993-02-23 | U.S. Philips Corp. | Method of manufacturing optical fibres |
| NL1023438C2 (en) * | 2003-05-15 | 2004-11-22 | Draka Fibre Technology Bv | Method for manufacturing an optical fiber, preform and an optical fiber. |
| NL1033769C2 (en) * | 2007-04-27 | 2008-10-28 | Draka Comteq Bv | Method for manufacturing a preform and method for manufacturing optical fibers from such a preform. |
| NL1034058C2 (en) * | 2007-06-29 | 2008-12-30 | Draka Comteq Bv | Method for manufacturing a preform and method for manufacturing optical fibers from such a preform. |
| EP2199263A1 (en) | 2008-12-19 | 2010-06-23 | Draka Comteq B.V. | Method and device for manufacturing an optical preform |
| EP2502887A1 (en) | 2011-03-25 | 2012-09-26 | Draka Comteq B.V. | Method of manufacturing an optical fibre, preform and optical fibre. |
| DE102012106478A1 (en) | 2012-07-18 | 2014-01-23 | J-Fiber Gmbh | A method of making a preform for a gradient index multimode fiber using an inner wall tube separation |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2619397B1 (en) * | 1987-08-12 | 1989-11-10 | Commissariat Energie Atomique | PROCESS FOR COVERING A LARGE LENGTH OF A UNIFORM LAYER OF PARTICLES |
| US7003984B2 (en) | 2001-04-30 | 2006-02-28 | Verrillon, Inc. | Hybrid manufacturing process for optical fibers |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4217027A (en) * | 1974-02-22 | 1980-08-12 | Bell Telephone Laboratories, Incorporated | Optical fiber fabrication and resulting product |
| JPS597649B2 (en) * | 1976-07-05 | 1984-02-20 | 日本電気株式会社 | Manufacturing method of optical fiber material |
| JPS53108445A (en) * | 1977-03-03 | 1978-09-21 | Fujitsu Ltd | Preparation of glass for optical transmission wire |
| US4302230A (en) * | 1980-04-25 | 1981-11-24 | Bell Telephone Laboratories, Incorporated | High rate optical fiber fabrication process using thermophoretically enhanced particle deposition |
| JPH05264938A (en) * | 1992-03-19 | 1993-10-15 | Fujitsu Ltd | Optical waveguide device |
-
1983
- 1983-03-16 EP EP19830901467 patent/EP0105327A4/en not_active Withdrawn
- 1983-03-16 WO PCT/US1983/000364 patent/WO1983003600A1/en not_active Ceased
- 1983-03-16 AU AU14777/83A patent/AU1477783A/en not_active Abandoned
- 1983-03-16 JP JP58501404A patent/JPS59500512A/en active Pending
- 1983-03-22 CA CA000424180A patent/CA1188102A/en not_active Expired
- 1983-04-07 GB GB08309433A patent/GB2118165A/en not_active Withdrawn
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4741747A (en) * | 1984-12-12 | 1988-05-03 | U.S. Philips Corporation | Method of fabricating optical fibers |
| EP0187405A3 (en) * | 1984-12-12 | 1988-06-01 | Philips Patentverwaltung Gmbh | Process for producing optical fibres |
| US5188648A (en) * | 1985-07-20 | 1993-02-23 | U.S. Philips Corp. | Method of manufacturing optical fibres |
| EP0209945A1 (en) * | 1985-07-20 | 1987-01-28 | Philips Patentverwaltung GmbH | Method for making optical fibres |
| US7522800B2 (en) | 2003-05-15 | 2009-04-21 | Draka Comteq B.V. | Method for the production of an optical fibre, preform, and an optical fibre |
| NL1023438C2 (en) * | 2003-05-15 | 2004-11-22 | Draka Fibre Technology Bv | Method for manufacturing an optical fiber, preform and an optical fiber. |
| WO2004101458A1 (en) * | 2003-05-15 | 2004-11-25 | Draka Fibre Technology B.V. | Optical fibre and preform and method of their manufacture |
| US7068899B2 (en) | 2003-05-15 | 2006-06-27 | Draka Fibre Technology B.V. | Method for the production of an optical fibre, preform, and an optical fibre |
| NL1033769C2 (en) * | 2007-04-27 | 2008-10-28 | Draka Comteq Bv | Method for manufacturing a preform and method for manufacturing optical fibers from such a preform. |
| EP1988064A1 (en) * | 2007-04-27 | 2008-11-05 | Draka Comteq B.V. | A method for manufacturing a preform as well as a method for forming optical fibres such a preform |
| US7930903B2 (en) | 2007-04-27 | 2011-04-26 | Draka Comteq B.V. | Method for manufacturing a preform as well as a method for forming optical fibres from such a preform |
| EP2008979A1 (en) | 2007-06-29 | 2008-12-31 | Draka Comteq B.V. | A method for manufacturing a preform as well as a method for forming optical fibres from such a preform |
| NL1034058C2 (en) * | 2007-06-29 | 2008-12-30 | Draka Comteq Bv | Method for manufacturing a preform and method for manufacturing optical fibers from such a preform. |
| EP2199263A1 (en) | 2008-12-19 | 2010-06-23 | Draka Comteq B.V. | Method and device for manufacturing an optical preform |
| US9051205B2 (en) | 2008-12-19 | 2015-06-09 | Draka Comteq, B.V. | Method and device for manufacturing an optical preform |
| EP2502887A1 (en) | 2011-03-25 | 2012-09-26 | Draka Comteq B.V. | Method of manufacturing an optical fibre, preform and optical fibre. |
| US8904827B2 (en) | 2011-03-25 | 2014-12-09 | Draka Comteq B.V. | Method of manufacturing an optical fibre, preform and optical fibre |
| DE102012106478A1 (en) | 2012-07-18 | 2014-01-23 | J-Fiber Gmbh | A method of making a preform for a gradient index multimode fiber using an inner wall tube separation |
| DE102012106478B4 (en) * | 2012-07-18 | 2015-03-05 | J-Fiber Gmbh | A method of making a preform for a gradient index multimode fiber using an inner wall tube separation |
| US9249046B2 (en) | 2012-07-18 | 2016-02-02 | j-fiber, GmbH | Methods for making a graded-index multimode preform and fiber |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0105327A1 (en) | 1984-04-18 |
| WO1983003600A1 (en) | 1983-10-27 |
| EP0105327A4 (en) | 1984-08-10 |
| CA1188102A (en) | 1985-06-04 |
| AU1477783A (en) | 1983-11-04 |
| JPS59500512A (en) | 1984-03-29 |
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| WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |