|Publication number||USRE30635 E|
|Application number||US 06/079,847|
|Publication date||Jun 2, 1981|
|Filing date||Sep 28, 1979|
|Priority date||Sep 14, 1974|
|Also published as||DE2444100A1, DE2444100B2, DE2444100C3|
|Publication number||06079847, 079847, US RE30635 E, US RE30635E, US-E-RE30635, USRE30635 E, USRE30635E|
|Inventors||Dieter Kuppers, Hans Lydtin, Ludwig Rehder|
|Original Assignee||U.S. Philips Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (9), Non-Patent Citations (1), Referenced by (51), Classifications (18), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This is a continuation of application Ser. No. 610,570, filed Sept. 5, 1975, now abandoned.
The invention relates to a method for producing internally coated glass tubes, consisting of a core and a jacket of glasses which have a mutually different refractive index, by means of a reactive deposition of the coating from a gas mixture which is passed through the tube and which is brought to reaction in the tube.
The tubes produced in this manner are heated to a temperature which is suitable for drawing and thereafter drawn to such an extent that the diameter is reduced until the coating is brought to coincidence and a light conductor of the required diameter is obtained.
Light conductors consist of a light-conducting core which is embedded in a jacket of a lower refractive index. The core may, for example, consist of quartz glass which has been doped with a few percent of a metal oxide which increases the refractive index and the jacket of undoped quartz glass.
For the doping of the core glass TiO2, GeO2 and Al2 O3 may, for example, be used. In the so-called self-focussing fibre optic light conductors a parabolic change in the refractive index across the radius is obtained by means of a continuous change in the grades of doping. According to a known method such internally coated quartz glass tubes are produced in which gaseous SiCl4 and oxygen or a mixture of SiCl4, TiCl4 and oxygen are passed through a tube brought there to reaction in the gas phase by means of high frequency energization and probably precipitated at least partly as a soot-like glass coat, which must thereafter be melted or sintered. There is a danger that gases are trapped which later on might form light-scattering centers. The heat treatment makes the formation of a doping profile as required for self-focussing fibre optic light conductors difficult, owing to blurring due to diffusion.
The tube may consist of non-doped quartz glass. In this method a uniform relative motion in .Iadd.an .Iaddend.axial direction may be caused between the tube and a high frequency pulse which envelopes the tube .[.a.]..Iadd.. A .Iaddend.uniform distribution of the deposit is enhanced by the fact that the tube is rotated during the coating procedure.
It is an object of the invention to provide a method of the aforementioned kind in which the rate of deposition is relatively large, in which coatings of a good quality are obtained and .[.that.]. .Iadd.in which .Iaddend.the deposition is not the result of a homogeneous reaction in the gas phase but of a heterogeneous reaction on the wall. According to the invention this object is realized by means of a method which is characterized in that in the tube a non-isothermal plasma zone is produced for the activation of the reactive deposition while a relative motion is caused between the tube and the equipment which produces the plasma, and a temperature zone in which the tube is heated to such a temperature that the deposited coatings are stress-free is superimposed on the plasma zone and that deposition takes place at a pressure of between 1 and 100 Torr.
In this respect a non-isothermal plasma is understood to mean a zone in which the kinetic energy of the gas particles is small compared with the energy of the excited electronic states. In spite of the low translational energy, many dissociated and ionised particles are available, which are favourable for the reaction and promote it.
With the method according to the invention well-adhering, crackfree or substantially crackfree coatings are formed on the tube wall. This is probably explained by the fact that in the method according to the invention the precipitation of the doped quartz glass takes .Iadd.place .Iaddend.mainly .[.place.]. on the tube wall and no or practically no soot-like particles are formed in the gas atmosphere. However it appeared that at pressures over 100 Torr the non-isothermal plasma gradually changes into an isothermal plasma and that the reactive deposition also takes place in gas while glass soot is formed.
The method according to the invention also enables the direct reactive deposition on a quartz wire or quartz rod which is arranged inside the tube.
With the method according to the invention deposition rates of from 2500 μm/hour can be attained. The method according to the invention makes it .[.therefore.]. possible .Iadd.therefore, .Iaddend.to obtain in an economic way a uniform deposition over long tube lengths.
In the method according to the invention a heating up of the tube (temperature zone) of greater length is superimposed on the plasma zone. The temperature shall then not be chosen that high that a homogeneous gas reaction could take place, but it must at least be chosen that high that the deposited coatings are stress-free. Heating of the tube to a temperature of between 800° C. and 1200° C., for example in the GeCl4 /oxygen system, does not or to only a small extent affect the deposition rate. In the temperature zone the consistency of the deposited coating is favourably influenced on the one hand because, at the chosen temperatures the mobility of the deposited matter is still sufficient to obtain a stress-free coat and on the other hand because the embedding of gaseous reaction products is avoided.
At temperatures which are too low, in general below 800° C. gases such as chlorine produced during the reaction may be trapped. At temperatures over 1200° C. reaction in the gas phase .Iadd.also .Iaddend.takes .[.also.]. place while soot-like particles are formed at the same time.
The plasma may be produced in any way, known in the art, for example by the inductive or capacitive coupling of a high frequency field or in a microwave resonator.
The invention will be further explained with reference to the drawing and the following examples.
In the drawing
FIG. 1 is a diagrammatic representation of a device for performing the method according to the invention;
FIG. 2 shows the attenuation of a fibre optic light conductor drawn from a tube produced according to the invention.
A tube 1, for example made of quartz is moved to a heating device 2, for example an electric heating coil in the direction indicated by arrows. The heating device 2 is enveloped by a resonator 3 by means of which a plasma 4 can be produced in the gas mixture passed through the quartz tube 1.
In the reactive deposition a coating 5 is directly formed on the inner wall of the tube 1.
The deposition of non-doped SiO2. A gas mixture consisting of SiCl4 and oxygen was passed through a quartz tube 1 (length 150 cm, outer diameter=8 mm, inner diameter=6 mm) at a throughput of 545 cm3 /minute. The mixture consisted of 7 volume % SiCl4 and 93 volume % oxygen. The pressure in tube 1 was 12 Torr. The wall temperature was kept at 1000° C. The tube 1 was passed at a speed of 0.17 cm per minute through the device, formed by heating device 2 having a length of 500 mm and resonator 3 having a length of 30 mm, while a plasma 4 was produced by a 2.45 GHz generator. An SiO2 coating having a thickness of 130 μm was formed directly on the tube wall. A gas phase reaction together with the formation of soot-like particles did not take place. The reaction efficiency in the plasma 4 is then almost 100%. The coating formed adheres well and is homogeneous. The gas mixture was measured in scm3 (standard cubic centimeters). 1 scm3 is one cm3 of the gas, where P=760 mm and T=0° C.
The deposition of an SiO2 -coat doped with GeO2. A mixture of SiCl4 and oxygen, consisting of 4 volume % SiCl4 and 96 volume % oxygen was used to which increasing linearly with time, GeCl4 was added until the content of GeCl4 was 0.4% by volume. The pressure was 10 Torr. The wall temperature was kept at 960° C. The throughput was 40 scm3 /minute and the duration of the test was 2 hrs. A well-adhering SiO2 coat doped with GeO2 was obtained. The coating consisted of 940 single layers of an increasing GeO2 content .Iadd.toward a central axis of the tube.Iaddend.. The resonator 3 was moved forward and backward along the tube in this test at 60 cm/min.
A mixture of 0.4 volume % AlCl3, 4 volume % SiCl4 and .Badd.95.6 volume % oxygen was passed through the quartz tube at a throughput of 42 scm3 per minute (length and diameter as in Example I). The pressure in the tube 1 was 15 Torr. The wall temperature of the tube 1 was kept at 950° C. A plasma 4 as in Example I was produced. (Power 180 W, frequency 2.45 GHz). The reaction efficiency was approximately 100%. The tube was passed through the device 2-3 at a speed of 60 cm per minute while the resonator 3 was moved forward and backward along the tube 1. A homogeneous, adhering coat 5 was obtained. The total thickness of the coating was 150 μm.
FIG. 2 shows the total attenuation in dB per km as a function of the wavelength in micrometer of a fiber optic light conductor which was obtained by drawing at 1900° C. of an internally coated tube according to Example II. The core diameter was 25 μm and the fiber diameter was 100 μm. The difference in the refractive indexes were approximately 5 o/oo.
By means of the method according to the invention a coating profile which has a certain refractive index in proportion to the doping can be obtained as shown above at a progressive change of the doping share. When a suitable profile is chosen the tube forms in an ideal manner a basic product for the production of monomode, multimode and self-focussing fiber optics.
.Iadd.Dopant-forming compounds which may be used in the method according to the invention are, for example, GeCl4, TiCl4, and AlCl3 which oxidize to form the dopants GeO2, TiO2, and Al2 O3, respectively.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3484276 *||Jul 21, 1966||Dec 16, 1969||Philips Corp||Apparatus for and method of providing a melted insulating coating on the inner surface of a tubular article|
|US3711262 *||May 11, 1970||Jan 16, 1973||Corning Glass Works||Method of producing optical waveguide fibers|
|US3932162 *||Jun 21, 1974||Jan 13, 1976||Corning Glass Works||Method of making glass optical waveguide|
|US3934061 *||Jul 18, 1973||Jan 20, 1976||Corning Glass Works||Method of forming planar optical waveguides|
|US3938974 *||Apr 22, 1974||Feb 17, 1976||Macedo Pedro B||Method of producing optical wave guide fibers|
|US3957474 *||Apr 17, 1975||May 18, 1976||Nippon Telegraph And Telephone Public Corporation||Method for manufacturing an optical fibre|
|US3961926 *||Dec 27, 1974||Jun 8, 1976||International Telephone And Telegraph Corporation||Preparation of germania cores in optical fibers|
|US4011006 *||Dec 17, 1975||Mar 8, 1977||Bell Telephone Laboratories, Incorporated||GeO2 -B2 O3 -SiO2 Optical glass and lightguides|
|CA622011A *||Jun 13, 1961||Lumalampan Ab||Producing oxide coatings on glass surfaces|
|1||Powell, C. F., et al., Vapor Deposition The Electrochemical Society, John Wiley and Son, Inc., New York (1966), p. 424.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
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|US5133794 *||Jul 11, 1991||Jul 28, 1992||U.S. Philips Corp.||Method of manufacturing optical fibres|
|US5188648 *||Oct 16, 1991||Feb 23, 1993||U.S. Philips Corp.||Method of manufacturing optical fibres|
|US6574994 *||Jun 18, 2001||Jun 10, 2003||Corning Incorporated||Method of manufacturing multi-segmented optical fiber and preform|
|US6764714||Jun 11, 2002||Jul 20, 2004||Southwest Research Institute||Method for depositing coatings on the interior surfaces of tubular walls|
|US6802190 *||Dec 11, 2002||Oct 12, 2004||Lucent Technologies Inc.||Method of fabricating a GRIN fiber|
|US7052736||Mar 23, 2004||May 30, 2006||Southwest Research Institute||Method for depositing coatings on the interior surfaces of tubular structures|
|US7092611||Aug 28, 2002||Aug 15, 2006||Draka Fibre Technology B.V.||Method for manufacturing a bar-shaped preform as well as a method for manufacturing optical fibres from such a bar-shaped preform|
|US7351480||Oct 24, 2003||Apr 1, 2008||Southwest Research Institute||Tubular structures with coated interior surfaces|
|US7526177||Jul 3, 2007||Apr 28, 2009||Draka Comteq B.V.||Fluorine-doped optical fiber|
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|US8252387 *||Dec 10, 2007||Aug 28, 2012||Ofs Fitel, Llc||Method of fabricating optical fiber using an isothermal, low pressure plasma deposition technique|
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|US8798423||May 25, 2012||Aug 5, 2014||Draka Comteq, B.V.||Single-mode optical fiber|
|US8798424||Jun 8, 2012||Aug 5, 2014||Draka Comteq B.V.||Single-mode optical fiber|
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|US20040115377 *||Oct 24, 2003||Jun 17, 2004||Ronghua Wei||Tubular structures with coated interior surfaces|
|US20110308461 *||Aug 17, 2010||Dec 22, 2011||Walton Scott G||Electron Beam Enhanced Nitriding System (EBENS)|
|DE3720029A1 *||Jun 16, 1987||Dec 29, 1988||Philips Patentverwaltung||Process for the production of optical fibres|
|EP0117009A1||Feb 20, 1984||Aug 29, 1984||Philips Electronics N.V.||Method of making a solid preform for drawing optical fibres|
|EP0129291A1 *||Jun 13, 1984||Dec 27, 1984||Philips Electronics N.V.||Method of and device for manufacturing optical fibres|
|EP0132011A2 *||Jul 11, 1984||Jan 23, 1985||Philips Patentverwaltung GmbH||Process for producing fibre light guides|
|EP0270157A1 *||Nov 5, 1987||Jun 8, 1988||Philips Electronics N.V.||Apparatus for coating the inside of a tube with glass|
|EP0295745A2 *||Jun 9, 1988||Dec 21, 1988||Philips Patentverwaltung GmbH||Method for making optical fibers|
|EP2527893A1||May 27, 2011||Nov 28, 2012||Draka Comteq BV||Single mode optical fiber|
|EP2533082A1||Jun 9, 2011||Dec 12, 2012||Draka Comteq BV||Single mode optical fiber|
|EP2541292A1||Jul 1, 2011||Jan 2, 2013||Draka Comteq BV||Multimode optical fibre|
|WO2009062131A1||Nov 9, 2008||May 14, 2009||Draka Comteq Bv||Microbend- resistant optical fiber|
|WO2015092464A1||Dec 20, 2013||Jun 25, 2015||Draka Comteq Bv||Single mode fibre with a trapezoid core, showing reduced losses|
|U.S. Classification||427/573, 138/145, 427/255.18, 427/575, 204/164, 427/167, 65/417, 427/237, 427/231, 427/255.24, 138/177, 385/124, 427/255.19, 65/391|
|International Classification||C03B37/018, G02B6/00|
|May 5, 1998||AS||Assignment|
Owner name: PLASMA OPTICAL FIBRE B.V., NETHERLANDS
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:U.S. PHILIPS CORPORATION;REEL/FRAME:009207/0784
Effective date: 19980430