GB2158263A - Optical fibre - Google Patents
Optical fibre Download PDFInfo
- Publication number
- GB2158263A GB2158263A GB08510656A GB8510656A GB2158263A GB 2158263 A GB2158263 A GB 2158263A GB 08510656 A GB08510656 A GB 08510656A GB 8510656 A GB8510656 A GB 8510656A GB 2158263 A GB2158263 A GB 2158263A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fibre
- optical fibre
- protective covering
- hydrogen
- powder
- 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.)
- Granted
Links
- 239000013307 optical fiber Substances 0.000 title claims abstract description 32
- 239000000835 fiber Substances 0.000 claims abstract description 56
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 56
- 239000001257 hydrogen Substances 0.000 claims abstract description 56
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 53
- 239000011248 coating agent Substances 0.000 claims abstract description 30
- 238000000576 coating method Methods 0.000 claims abstract description 30
- 230000001681 protective effect Effects 0.000 claims abstract description 28
- 229910052751 metal Inorganic materials 0.000 claims abstract description 24
- 239000000843 powder Substances 0.000 claims abstract description 21
- 238000010521 absorption reaction Methods 0.000 claims abstract description 17
- 239000011347 resin Substances 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 14
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 4
- 230000000737 periodic effect Effects 0.000 claims abstract description 4
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 4
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 4
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 239000011521 glass Substances 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910045601 alloy Inorganic materials 0.000 claims description 4
- 239000000956 alloy Substances 0.000 claims description 4
- 229910000765 intermetallic Inorganic materials 0.000 claims description 4
- 229920002379 silicone rubber Polymers 0.000 claims description 4
- 239000004945 silicone rubber Substances 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 3
- 150000002602 lanthanoids Chemical class 0.000 claims description 3
- 229910052758 niobium Inorganic materials 0.000 claims description 3
- 239000010955 niobium Substances 0.000 claims description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 3
- 238000010073 coating (rubber) Methods 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 2
- 229910052774 Proactinium Inorganic materials 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 7
- 238000005253 cladding Methods 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000007669 thermal treatment Methods 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000010301 surface-oxidation reaction Methods 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- G02B6/44—Mechanical structures for providing tensile strength and external protection for fibres, e.g. optical transmission cables
- G02B6/4401—Optical cables
- G02B6/4402—Optical cables with one single optical waveguide
-
- 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
- G02B6/44—Mechanical structures for providing tensile strength and external protection for fibres, e.g. optical transmission cables
- G02B6/4401—Optical cables
- G02B6/4429—Means specially adapted for strengthening or protecting the cables
- G02B6/44382—Means specially adapted for strengthening or protecting the cables the means comprising hydrogen absorbing materials
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
Abstract
An optical fibre 1 is protected against the absorption of hydrogen by a covering (3,9), which comprises at least one metallic element of Group III, IV, V, or VIII of the periodic system (e.g. Ti, Zr, Hf, Va, Ni, Ta, Pa). In one embodiment this covering comprises a metallized layer disposed on the fibre immediately adjacent the outer surface thereof (see Fig. 1 not shown) or adjacent a further protective covering (2) - or the metallic element may be present as a powder in a resin coating (3,9). In a further embodiment, the covering may be a loose tube (9) surrounding the fibre (1,2). The metallic element being present also or alternatively as a gel or powder filling the tube. <IMAGE>
Description
SPECIFICATION
Optical fibre
The present invention relates to optical fibres, and particularly to such fibres for telecommunications cables.
Generally, optical fibres used for telecommunications cables comprise a glass structure formed by a cladding disposed over a core, for example of the "step index" or "graded index type, and a primary coating applied to the fibre over the cladding thereof immediately after its formation to prevent the fibres having direct contact with the environment. Over this primary coating other protective coverings are applied, for example, a layer of silicone rubber and a more rigid layer or tube made, for example, of nylon. An optical fibre telecommunications cable generally comprises one or more such optical fibres housed inside a sheath, together with one or more tensile-resistant members. The sheath, which may be metallic, is provided with one or more coverings such as armouring.
It has been found that exposure of an optical fibre to gaseous hydrogen causes a deterioration in its properties, for example the attenuation of the signal being transmitted is increased and the mechanical properties of the fibre are lowered, In cables comprising one or more optical fibres, the hydrogen which acts on the fibres to cause this deterioration may be generated from parts of the cable itself or from external sources Generally, the first effect of a fibre's exposure to hydrogen to become apparent is the increase in the attenuation of the signal being transmitted. This increased attenuation occurs particularly in signals being transmitted with wavelengths of over 1 micron, that is in signals having wavelengths typically used in telecommunications optical fibre cables.
From the tests we have carried out we have established that the increase in attenuation may be caused in two ways. Firstly, by hydrogen itself which when diffused in the optical fibre is capable of absorbing energy with an absorption spectrum comprising the wavelengths used for the optical signal. Under certain circumstances, this phenomenon is reversible by causing or allowing the hydrogen in the fibre causing the increased attenuation to diffuse out of the fibre (for example by lowering the hydrogen concentration external to the fibre which originated the phenomenon).The second way in which hydrogen may cause the increase in attenuation is by the hydrogen, when diffused in the fibre, chemically reacing with the constituents of the fibre (for example (SiO2) and/or its aopants (for example GeO2, P205 etc) to form groups containing the hydroxyl radical (OH) that are able to absorb signals of other wavelengths used.
These chemical reactions are not reversible and hence increased attenuation of the signals caused thereby can be expected to be permanent under any conditions in which hydrogen is present. The factors which govern both causes of increased attenuation are, in addition to the chemical composition of the fibre, the partial pressure of the hydrogen to which the fibre is exposed, temperature and time.
The cable fibres may be exposed to hydrogen which is generated during the manufacture of the cable and/or during the operation of the cable. Hydrogen can be generated by the presence of metallic or non-metallic parts of the cable which have absorbed the hydrogen during production, refining and finishing of the materials of the cable. Hydrogen can be generated due to the eventual chemical degradation through oxidation of the organic materials present in the cable, or through the oxidation of metallic materials of the cable by water (either in its liquid state or as a vapour).
Furthermore, certain organic materials which are sometimes used in the cladding or to coat the fibres themselves are capable of chemically reacting to produce hydrogen. One cource of hydrogen has been found to be a slicone rubber covering of the fibre, possibly due to the construction of the cross-linking process. Although the hydrogen produced by the cladding or coverings of the fibres is able to diffuse away from as well as towards the fibre, when the fibres are disposed within the cable sheath, and particularly when there is a limited amount of free space within the cable, disperson away from the fibres is limited.
The rate of diffusion of hydrogen through the materials of the cable varies. It is lowest through metals, greater through polymers, greater still through liquids and greatest through gases. Hence depending upon the type of cable and the environment in which it is situated there will be various emission rates for the hydrogen generated by the parts of the cable and also various rates at which the hydrogen is absorbed into the environment.
The partial pressure of the hydrogen within the cable depends on these rates and is therefore a function of time. The greater the partial pressure and the longer the fibre is exposed to hydrogen the greater the risk of it deteriorating due to it absorbing hydrogen.
In general it is necessary for each case to take into consideration the production rate of hydrogen (originating either inside or outside the cable), the diffusion rate of hydrogen through the cable sheath and the rate at which hydrogen is dispersed through the environment in order to establish what the partial pressure of the hydrogen will be in the proximity of the optical fibres both in an initial transient period and thereafter in steady state conditions. For example given the typical service lifetime for an optical fibre cable the diffusion rate of hydrogen through metals is so low under typical service temperatures and pressures that a metallic sheath of the cable can be considered to be practically impermeable to hydrogen.Thus the optical fibres of cables having metallic sheaths especially of small inner diameter, are particularly susceptible to deterioration due to absorption of hydrogen generated by the cable parts and significant increases in the attenuation of signals being transmitted thereby occur within a relatively short time.
An object of the present invention is to provide an optical fibre with means of protection against the absorption of hydrogen which may be present in the cable in which the fibre is located, in use. This is broadly achieved by having present in at least one covering of the fibre a,t least one metallic element which is capable of absorbing and combining with any hydrogen gas within the cable.
The invention includes an optical fibre having at least one protective covering, wherein the or at least one said protective covering comprises at least one metallic element of
Group Ill, IV, V, or VIII of the periodic system for protecting the fibre against the absorption of hydrogen.
Among these metallic elements the following have been found particularly suitable: any one of the Lanthanides, Titanium, Zirconium,
Hafnium, Vanadium, Niobium, Tantalum, and
Palladium, and any one may be present in the or each protective covering as a pure metal, in an alloy or in an intermetallic compound.
In the presence of hydrogen, the aboveindicated elements tend to form solid interstitial solutions which are comparable to hydrides and have a good stability, thus reducing the partial pressure of the hydrogen in the cable to values that balance with the hydrogen solubility in the elements themselves.
By utilising appropriate quantities of one or more of these elements, one can succeed in limiting the residual pressure of hydrogen in the cable, to values at which the hydrogen's effect on the fibre's properties and in particu
lar, upon the increase in attenuation caused thereby, is negligible throughout the entire design service life of the cable.
Preferably the above-stated elements, in whatever form they are present in the cable, are subjected to thermal treatment under vacuum, at a temperature of a few hundred
degrees Celcius, e.g. over 1 600 C, since it
has been found that after such a thermal treatment, the above-indicated elements are
better able to absorb hydrogen, particularly at
low partial pressures. It is assumed that these
elements may, in some cases, already contain
a certain amount of hydrogen and/or other
gases which are absorbed during the manufacturing, purification and finishing processes
of the elements in the form used in the cable,
and that they have a certain level of surface
oxidation.Both these phenomena could re
duce the ability of the elements to absorb hydrogen, and the thermal treatment referred to above which is carried out at temperatures with are approximate to, but less than, the melting temperature of the elements, perform degasification and/or the elimination of the surface oxidation through sublimation.
In order that the invention may be better understood some embodiments thereof, which are given by way of example only, will now be described with reference to the accompanying drawings, in which:
Figure 1 schematially shows a cross-section of an optical fibre provided with a primary metallic coating;
Figure 2 schematically shows a cross-section of an optical fibre provided with a primary coating;
Figure 3 schematically shows a cross-section of an optical fibre provided with a primary and a secondary coating;
Figure 4 schematically shows a cross-section of an optical fibre provided with a primary and a secondary coating, between which there is interposed a cushioning layer; and
Figure 5 schematically shows a cross-section of an optical fibre provided with a loose covering, or jacket.
In each of the illustrated embodiments the optical fibre is illustrated at 1 and is provided with at least one protective covering which comprises at least one metallic element of
Group III, IV, V, or Vlil of the periodic system and preferably at least one of the Lanthanides,
Titanium, Zirconium, Hafnium, Vanadium,
Niobium, Tantalium or Palladium, which are
referred to hereinafter as 'the cited metallic elements'. Any one of the cited metallic ele
ments may be used as a pure metal, in an alloy, or in an intermetallic compound.
In a first embodiment, shown in Fig. 1, the
protective covering comprising at least one of the cited metallic elements is a metallized
layer 2 which forms a primary coating 2 of the fibre and is disposed on the fibre immedi
ately adjacent the outer surface of the glass
structure of the optical fibre. Thus the
metallized layer not only performs the me
chanical function of the usual primary coating
of the fibre but also protects the fibre against
the absorption of hydrogen. The fibre will
normally be provided with one or more further
protective coverings. In a non-illustrated varia
tion the metallizing layer is applied immedi
ately over the usual cross-linked resin primary
coating. This construction is beneficially utili
zable when it is either not possible or not
convenient to modify existing fibre producing
plant which applies a resin primary coating to
the fibre immediately after the fibre is drawn.
It will also be appreciated that the
metallized layer may be disposed on one or
more of any of the other protective coverings
of the fibre.
In second, third and fourth embodiments
shown in Figs. 2 to 4 at least one of the cited metallic elements is present in a powder in a resin coating of the fibre as a pure metal, in an alloy or in an intermetallic compound. The particles of the powder are preferably less than 10 microns in diameter and are present in the resin coating with a concentration of from 0.1 to 10 parts per hundred of resin.
In the second embodiment, illustrated in
Fig. 2, the powder is disposed in the primary coating 2 which is disposed on the fibre immediately adjacent the outer glass surface thereof and which comprises an acrylic resin, or other suitable resin. As will be appreciated the powder may be readily added to the resin material used for the primary coating and this may be applied in the conventional way.
Therefore this embodiment provides a very convenient way of protecting the fibre against the absorption of hydrogen.
In the third embodiment, shown in Fig. 3, the powder is disposed in the coating 3 immediately surrounding the primary. coating 2. This coating 3 is typically formed of silicone rubber which, as explained previously, may be a source of hydrogen which is particularly significant in view of its proximity to the fibre. The presence of the powder is this coating can effectively neutralize the hydrogen generated therein before it can diffuse towards the fibre.
In the fourth embodiment illustrated in Fig.
4, a secondary coating 4 formed, for example, of nylon or some other thermoplastic polymer, is provided on the fibre over the primary coating 2 with a cushioning layer 3 interposed therebetween. The powder in this embodiment is disposed in the coating 4.
It will be appreciated that the presence of the powder in the covering adjacent the outer glass surface of the optical fibre, primarily protects the fibre from absorption of any hydrogen generated in the protective covering of the fibre and particularly the innermost coverings thereof, while the presence of the powder in an outer protective covering (for example the silicone rubber coating 3 in Fig. 3) primarily protects the fibre from absorption of any hydrogen generated by the cable elements. It will therefore be appreciated that in certain circumstances it may be desirable to provide the powder in more than one of the protective coverings of the fibre and to this end it is to be understood that the measures in the embodiments shown in Figs. 2 to 4 for protecting the fibre against absorption of hydrogen may be combined.
A fifth embodiment of the invention, shown in Fig. 5, relates to an optical fibre provided with a loose protective covering, or jacket.
The fibre 1 is shown with a primary coating 2, but may be provided with additional protective coatings or non-adherent coverings as typically used for loose jacketed fibres. The loose protective covering, or jacket, of the fibre is a platics tube 9, whose internal diameter is greater than the external diameter of the coated fibre. A gel having dispersed therein at least one of the cited metallic elements present in a powder is disposed in the space 8 between the tube 9 and the coated fibre and thus forms a protective covering of the fibre for protecting the fibre against the absorption of hydrogen. Additionally or alternatively at least one of the cited metallic elements may be present in a powder dispersed in the tube 9. It will also be appreciated thatçany of the other protective layers of the fibre may be provided with the measures described in the embodiments shown in Figs.
2 to 4 for protecting the fibre against absorption of hydrogen. It will also be understood that the use of a metallized layer for this purpose as described in relation to the embodiment shown in Fig. 1 and the variations thereof disclosed may be combined with any of the above described arrangements in which a powder containing at least one of the cited metallic elements is dispersed in a protective covering.
Claims (11)
1. An optical fibre having at least one protective covering, wherein the or at least one said protective covering comprises at least one metallic element of Group Ill, IV, V or
VIII of the periodic system for protecting the fibre against the absorption of hydrogen.
2. An optical fibre as claimed in claim 1, wherein the or a said hydrogen absorption protective covering comprises at least one of any one of the Lanthanides, Titanium, Zirconium, Hafnium, Vanadium, Niobium, Tantalum or Palladium, as a pure metal, in an alloy or in an intermetallic compound.
3. An optical fibre as claimed in claim 1 or 2, wherein the or at least one said hydrogen absorption protective covering comprises a metallized layer.
4. An optical fibre as claimed in claim 3, wherein the or a said metallized layer is disposed on the fibre immediately adjacent the outer surface thereof.
5. An optical fibre as claimed in claim 3 or 4, wherein the or a said metallized layer is disposed on at least one other protective covering of the fibre.
6. An optical fibre as claimed in claim 1 or 2, wherein the or at least one said hydrogen absorption protective covering comprises at least one of said metallic elements present in a powder in a resin coating of the fibre.
7. An optical fibre as claimed in claim 6, wherein the particles of said powder are less than 10 microns in diameter and are present in said resin coating with a concentration of from 0.1 to 10 parts per hundred of resin.
8. An optical fibre as claimed in claim 6 or 7, wherein the or a said resin coating containing said powder is disposed on the fibre immediately adjacent the outer glass surface thereof.
9. An optical fibre as claimed in claim 6, 7 or 8, wherein the or a said resin coating containing said powder is disposed immediately adjacent a protective covering which itself is disposed immediately adjacent the other glass surface of the fibre.
10. An optical fibre as claimed in claim 9, wherein the or said resin coating referred to in claim 9 comprises a silicone rubber coating.
11. An optical fibre as claimed in claim 1 or 2, with at least one protective covering formed as a coating and provided with a loose protective covering comprising a tube whose internal diameter is greater than the external diameter of the coated fibre, wherein the or at least one said hydrogen absorption protecting covering comprises a gel between the coated fibre and the tube having dispersed therein at least one of said metallic elements present in a powder.
1 2. An optical fibre as claimed in claim 1 or 2, with at least one protective covering formed as a coating and provided with a loose protective covering comprising a tube whose internal diameter is greater than the external diameter of the coated fibre, wherein the or at least one said hydrogen absorption protective covering comprises said tube which has dispersed therein at least one of said metallic elements present in a powder.
1 3. An optical fibre substantially as herein described with reference to any one of the figures of the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT20700/84A IT1176135B (en) | 1984-04-27 | 1984-04-27 | OPTICAL FIBER PROTECTED AGAINST GAS HYDROGEN ABSORPTION |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8510656D0 GB8510656D0 (en) | 1985-06-05 |
GB2158263A true GB2158263A (en) | 1985-11-06 |
GB2158263B GB2158263B (en) | 1988-01-06 |
Family
ID=11170753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08510656A Expired GB2158263B (en) | 1984-04-27 | 1985-04-26 | Optical fibre |
Country Status (13)
Country | Link |
---|---|
JP (1) | JPS60239703A (en) |
AU (1) | AU577574B2 (en) |
BR (1) | BR8501841A (en) |
CA (1) | CA1251075A (en) |
DE (1) | DE3515228A1 (en) |
FR (1) | FR2563634B1 (en) |
GB (1) | GB2158263B (en) |
GR (1) | GR851015B (en) |
IT (1) | IT1176135B (en) |
NL (1) | NL8500892A (en) |
NO (1) | NO168209C (en) |
NZ (1) | NZ211369A (en) |
SE (1) | SE462007B (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2172410A (en) * | 1985-03-13 | 1986-09-17 | Telephone Cables Ltd | Optical fibre cable containing hydrogen trapping powder |
FR2588388A1 (en) * | 1985-10-08 | 1987-04-10 | Pirelli Cavi Spa | OPTICAL FIBER TELECOMMUNICATIONS CABLE WITH INCORPORATED HYDROGEN ABSORBER MIXTURE, AND HYDROGEN ABSORBER MIXTURE FOR OPTICAL FIBER CABLE |
GB2183365A (en) * | 1985-11-19 | 1987-06-03 | Stc Plc | Hydrogen occlusion in optical cables |
GB2240189A (en) * | 1990-01-17 | 1991-07-24 | Telephone Cables Ltd | Optical cables |
GB2313330A (en) * | 1996-05-24 | 1997-11-26 | Perkin Elmer Ltd | Coating optical fibres |
EP0858082A1 (en) * | 1997-02-10 | 1998-08-12 | PIRELLI CAVI E SISTEMI S.p.A. | Moisture-resistant cable |
US6205276B1 (en) | 1997-02-10 | 2001-03-20 | Pirelli Cavi E Sistemi S.P.A. | Moisture-resistant cable including zeolite |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4108032A1 (en) | 1991-03-13 | 1992-09-17 | Bayer Ag | PALLADIUM-CONTAINING POLYMER COMPOSITION AND METHOD FOR THE PRODUCTION THEREOF |
US6404961B1 (en) | 1998-07-23 | 2002-06-11 | Weatherford/Lamb, Inc. | Optical fiber cable having fiber in metal tube core with outer protective layer |
FR2803045B1 (en) * | 1999-12-22 | 2002-10-11 | Cit Alcatel | OPTICAL FIBER AND FIBER OPTIC CABLE COMPRISING AT LEAST ONE HYDROGEN-ABSORBING INTERMETALLIC ELEMENT |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0034670A1 (en) * | 1980-02-12 | 1981-09-02 | The Post Office | A glass optical fibre and a method of coating a plastic coated glass fibre with metal |
WO1982001365A1 (en) * | 1980-10-14 | 1982-04-29 | Aircraft Co Hughes | Metallic clad fiber optical waveguide |
WO1982001543A1 (en) * | 1980-11-03 | 1982-05-13 | Aircraft Co Hughes | Multiply coated metallic clad fiber optical waveguide |
GB2125180A (en) * | 1982-08-10 | 1984-02-29 | Standard Telephones Cables Ltd | Optical fibre manufacture |
GB2144559A (en) * | 1983-08-05 | 1985-03-06 | Bicc Plc | Optical cables |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1079512A (en) * | 1978-11-16 | 1980-06-17 | Basil V.E. Walton | Powdered telephone cable filling compound |
JPS6082156A (en) * | 1983-10-13 | 1985-05-10 | ドル−オリバ− インコ−ポレイテツド | Hydrocyclone |
-
1984
- 1984-04-27 IT IT20700/84A patent/IT1176135B/en active
-
1985
- 1985-03-05 AU AU39535/85A patent/AU577574B2/en not_active Ceased
- 1985-03-08 NZ NZ211369A patent/NZ211369A/en unknown
- 1985-03-27 NL NL8500892A patent/NL8500892A/en not_active Application Discontinuation
- 1985-04-18 BR BR8501841A patent/BR8501841A/en unknown
- 1985-04-18 FR FR858505855A patent/FR2563634B1/en not_active Expired - Lifetime
- 1985-04-26 NO NO851686A patent/NO168209C/en unknown
- 1985-04-26 JP JP60090760A patent/JPS60239703A/en active Pending
- 1985-04-26 GB GB08510656A patent/GB2158263B/en not_active Expired
- 1985-04-26 DE DE19853515228 patent/DE3515228A1/en not_active Withdrawn
- 1985-04-26 GR GR851015A patent/GR851015B/el unknown
- 1985-04-26 SE SE8502047A patent/SE462007B/en not_active IP Right Cessation
- 1985-04-26 CA CA000480142A patent/CA1251075A/en not_active Expired
Patent Citations (6)
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EP0034670A1 (en) * | 1980-02-12 | 1981-09-02 | The Post Office | A glass optical fibre and a method of coating a plastic coated glass fibre with metal |
WO1982001365A1 (en) * | 1980-10-14 | 1982-04-29 | Aircraft Co Hughes | Metallic clad fiber optical waveguide |
WO1982001543A1 (en) * | 1980-11-03 | 1982-05-13 | Aircraft Co Hughes | Multiply coated metallic clad fiber optical waveguide |
GB2125180A (en) * | 1982-08-10 | 1984-02-29 | Standard Telephones Cables Ltd | Optical fibre manufacture |
GB2144559A (en) * | 1983-08-05 | 1985-03-06 | Bicc Plc | Optical cables |
GB2144878A (en) * | 1983-08-05 | 1985-03-13 | Bicc Plc | Optical cables |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2172410A (en) * | 1985-03-13 | 1986-09-17 | Telephone Cables Ltd | Optical fibre cable containing hydrogen trapping powder |
FR2588388A1 (en) * | 1985-10-08 | 1987-04-10 | Pirelli Cavi Spa | OPTICAL FIBER TELECOMMUNICATIONS CABLE WITH INCORPORATED HYDROGEN ABSORBER MIXTURE, AND HYDROGEN ABSORBER MIXTURE FOR OPTICAL FIBER CABLE |
GB2183365A (en) * | 1985-11-19 | 1987-06-03 | Stc Plc | Hydrogen occlusion in optical cables |
GB2183365B (en) * | 1985-11-19 | 1989-10-18 | Stc Plc | Hydrogen occlusion in optical fibre cables. |
GB2240189A (en) * | 1990-01-17 | 1991-07-24 | Telephone Cables Ltd | Optical cables |
GB2313330A (en) * | 1996-05-24 | 1997-11-26 | Perkin Elmer Ltd | Coating optical fibres |
EP0858082A1 (en) * | 1997-02-10 | 1998-08-12 | PIRELLI CAVI E SISTEMI S.p.A. | Moisture-resistant cable |
US6205276B1 (en) | 1997-02-10 | 2001-03-20 | Pirelli Cavi E Sistemi S.P.A. | Moisture-resistant cable including zeolite |
Also Published As
Publication number | Publication date |
---|---|
FR2563634B1 (en) | 1990-02-23 |
NZ211369A (en) | 1988-03-30 |
SE8502047L (en) | 1985-10-28 |
NO168209B (en) | 1991-10-14 |
NO851686L (en) | 1985-10-28 |
BR8501841A (en) | 1985-12-17 |
IT8420700A1 (en) | 1985-10-27 |
DE3515228A1 (en) | 1985-10-31 |
CA1251075A (en) | 1989-03-14 |
NO168209C (en) | 1992-01-22 |
NL8500892A (en) | 1985-11-18 |
GR851015B (en) | 1985-11-25 |
GB2158263B (en) | 1988-01-06 |
AU3953585A (en) | 1985-10-31 |
IT8420700A0 (en) | 1984-04-27 |
SE8502047D0 (en) | 1985-04-26 |
JPS60239703A (en) | 1985-11-28 |
SE462007B (en) | 1990-04-23 |
FR2563634A1 (en) | 1985-10-31 |
GB8510656D0 (en) | 1985-06-05 |
IT1176135B (en) | 1987-08-12 |
AU577574B2 (en) | 1988-09-29 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19930426 |