BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a method of fabricating an optical fiber preform
by hydrolyzing a glass raw material gas in flame to generate glass particles, and
depositing the particles on a rotating starting material.
Description of the Related Art
[0002] Up until now, various methods have been proposed for manufacturing optical fiber
preforms. Among these methods is an Outside Vapor Phase Deposition Method (OVD method).
In this method, glass particles generated by a burner flame are deposited and adhered
on a rotating starting material while relatively reciprocating the burner or the starting
material to synthesize a porous preform. The preform is desiccated and sintered in
an electric furnace. The foregoing method has been widely used because the method
can provide an optical fiber preform having a relatively arbitrary refractive index
distribution and can mass-produce preforms having a large diameter.
[0003] Fig. 1 shows an outline of one example of an apparatus for fabricating an optical
fiber preform. In the drawing, a starting material, on which glass particles (soot)
are deposited, is constituted by welding a dummy rod 2 at both ends of a core rod
1, and both ends are supported by an ingot chuck mechanism 4 so as to be rotatable
about an axis thereof. A freely movable burner 3 is arranged in the direction of the
starting material. Vapor of an optical fiber source material such as SiCl
4 and combustion gas (hydrogen gas and oxygen gas) are blown from the movable burner
to the starting material, and soot generated by the hydrolysis in an oxyhydrogen flame
is deposited on the starting material to form a porous optical fiber preform. Reference
numeral 5 represents an exhaust hood.
[0004] The burner 3 is supported by a burner guide mechanism (not shown) so as to be reciprocal
in a longitudinal direction of the starting material and retractable from the starting
material, and ejects a flame towards the starting material rotating about the axis.
By depositing glass particles generated by the hydrolysis of the source material gas
in the flame, a porous preform is fabricated. Next, by passing the porous preform
through a heater portion of a heating furnace (not shown), it is desiccated and vitrified
to become an optical fiber preform.
[0005] For synthesizing glass particles and depositing soot (glass particles) on a starting
material, a concentric multiple tube burner has been conventionally used. However,
the burner having such structure can not sufficiently mix a glass raw material gas,
a flammable or burnable gas and a combustion assisting gas to generate a sufficient
amount of glass particles. As a result, the manufacturing yield has not been improved
and it has been difficult to achieve a high-speed synthesis.
[0006] In order to solve the problem, Japanese Patent No.
1773359 has proposed a multi-nozzle type burner, in which a plurality of small diameter combustion
assisting gas-ejecting ports (hereinafter, referred to as small diameter ejecting
port) are arranged in a burnable gas-ejecting port so as to surround the central source
material gas-ejecting port.
[0007] Further, Japanese Patent No.
3543537 has proposed a method of preventing the disturbance of a source material gas flow,
in which, when denoting the focal length of a plurality of small diameter ejecting
ports by L1 and the distance from the tip of the small diameter ejecting port to the
glass particle deposition plane of a preform by L2, it is proposed that L1 is larger
than L2. Inversely, Japanese Patent Application Laying-Open No.
2003-226544 has disclosed that the deposition efficiency can be improved by making L1 smaller
than L2 to enhance the mixing efficiency of the gas.
[0008] However, in the OVD method, in which glass particles generated in a burner flame
are deposited and adhered onto a rotating starting material while causing the burner
or the starting material to relatively reciprocate, the weight of the preform increases
and the diameter of a deposited body increases as the deposition progresses. Accordingly,
as the deposition proceeds, the gas amount is usually increased to adjust the density
of the deposited body. The deposition is continued until a starting material having
an initial diameter of 50 mm attains a diameter of 300 mm.
[0009] During an early stage of deposition, since the deposition area is small, the deposition
is performed at a small linear velocity of gas with a small amount of gas supplied.
Consequently, the flow of glass particles is easily disturbed by gas ejected from
the small diameter ejecting ports, and the disturbance decreases the deposition efficiency.
In the second half of deposition, since the deposited body has an increased diameter
and the deposition area has increased, the deposition is performed at a large linear
velocity of gas with an increased amount of gas supplied. As a result, although the
disturbance of the flow of glass particles by gas ejected from the small diameter
ejecting ports is small, there is a problem that a large linear velocity of gas reduces
the mixing ratio of gases and thus the deposition efficiency is decreased.
[0010] JP-A-10101343 discloses a method for synthesizing fine glass particles and a focal burner therefor,
wherein groups of gaseous oxygen injection ports are concentrically arranged outside
a glass material injection port in the center and formed at one or plural specified
focal distances, and an annular gaseous hydrogen injection port enclosing the plural
gaseous oxygen injection ports are provided to the burner.
SUMMARY OF THE INVENTION
[0011] An object of the present invention is to solve the aforementioned problem and to
provide a method capable of effectively performing the generation and the deposition
of glass particles. In particular, the invention relates to a method of fabricating
an optical fiber preform that can provide a stable and highly efficient deposition
from the start to the end of the deposition upon synthesizing a large size preform.
[0012] According to a first aspect of the present invention, there is provided a method
of fabricating an optical fiber preform, comprising:
using a burner having a concentric multiple-tube structure and having at least a glass
raw material gas-ejecting port arranged at the center of the burner, a flammable gas
ejecting port arranged outside the glass raw material gas-ejecting port, and a plurality
of small diameter combustion assisting gas-ejecting ports arranged inside the flammable
gas-ejecting port in at least one line on concentric circles relative to the glass
raw material gas-ejecting port, the plurality of small diameter combustion assisting
gas-ejecting ports arranged on the same line having the same focal length in a concentric
fashion in such a way that the respective axes of the plurality of small diameter
combustion assisting gas-ejecting ports focus at one point;
ejecting the glass raw material gas from the glass raw material gas-ejecting port;
ejecting a flammable gas from the flammable gas-ejecting port arranged outside the
glass raw material gas-ejecting port;
ejecting a combustion assisting gas from the plurality of small diameter combustion
assisting gas-ejecting ports;
hydrolyzing a glass raw material gas ejected from the glass raw material gas-ejecting
port to generate glass particles;
depositing the glass particles on a rotating starting material in the radial direction,
setting the ratio of L1 and L2 to L1 > L2 during the early stage of the deposition, where the focal length of the plurality
of small diameter combustion assisting gas-ejecting ports is defined by L1 and the distance from the tip of the plurality of small diameter combustion assisting
gas-ejecting ports to a deposition plane of the glass particles on the starting material
is defined by L2; and
increasing L2 during the course of the deposition so that L2 is greater than L1 (L1 < L2), wherein the ratio L1 < L2 is achieved in the latter half of the deposition.
[0013] According to a second aspect of the present invention, there is provided a method
of fabricating an optical fiber preform wherein said burner is moved away from the
deposition plane of the glass particles on the starting material so that the distance
L
2 is made greater as an amount of deposition is increased to increase the outer diameter
of the preform so as to achieve the relationship of L
1 < L
2.
[0014] According to a third aspect of the present invention, there is provided a method
of fabricating an optical fiber preform, wherein said burner is moved away from the
deposition plane of the glass particles on the starting material so that a relationship
L1 = L2 is achieved when the outer diameter of the preform increases to substantially
three times the diameter of the starting material.
[0015] The present invention provides extremely excellent effects in continuing deposition
in a stable condition from start to the end with high deposition efficiency without
causing rapid change in the density.
[0016] Further features of the present invention will become apparent from the following
description of exemplary embodiments (with reference to the attached drawings).
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] Fig. 1 is a schematic view showing an outline of an apparatus for manufacturing a
porous glass preform by the Outside Vapor Phase Deposition Method (OVD method);
[0018] Fig. 2A is a schematic view showing the tip end of a burner for synthesizing glass
particles, having the small diameter ejecting ports for use in the present invention;
[0019] Fig. 2B is a cross-sectional view of the tip portion of the burner in Fig. 2A;
[0020] Fig. 3A is a drawing illustrating the relation between the focal length L
1 and the distance L
2 from the burner tip to the deposition plane during the early stage of the deposition;
[0021] Fig. 3B is a drawing illustrating the relation between the focal length L
1 and the distance L
2 from the burner tip to the deposition plane during the latter half of the deposition;
and
[0022] Fig. 4 is a graph illustrating the relation between deposition weight and deposition
rate.
DESCRIPTION OF THE EMBODIMENTS
[0023] In order to achieve the above described object, the present inventor has found, as
a result of the research, that it is important to properly set the relation between
the focal length of small diameter ejecting ports and the distance from the tip of
the ejecting ports to the deposition plane of glass particles during the early stage
of the deposition and during the latter half of the deposition, respectively, and
thus has achieved the present invention.
[0024] That is, in a burner shown in Figs. 2A and 2B, as shown in Figs. 3A and 3B, the focal
length of a gas flow ejected from a plurality of small diameter ejecting nozzles 106
arranged in a concentric circle fashion in such a way that the respective axes of
the nozzles 106 focus at one point is denoted by L
1. The distance from the tip of the ejecting nozzles 106 to a glass particle deposition
plane 107 is denoted by L
2. By setting L
1 > L
2 during the early stage of the deposition, during which the flow of glass particles
may easily be disturbed by the combustion assisting gas ejected from the ejecting
ports, it is possible to accelerate the mixing of the flammable gas with the combustion
assisting gas in the outer side of the central flow without disturbing the central
flow of glass particles. Thus, the deposition efficiency is increased.
[0025] In the present invention, the latter half of the deposition may be defined as a time
period from the time that the diameter of a deposited body has grown to substantially
three times that of the starting material.
[0026] By contrast, during the latter half deposition where the amount of gas and the linear
velocity of the gas flow have been increased, the glass particle flow is hardly influenced
by the combustion assisting gas flow ejected from the small diameter ejecting nozzles
106 and is hardly disturbed, but, on the other hand, the gas mixing efficiency is
degraded. Therefore, by setting L
1 < L
2, the combustion assisting gas from the small diameter ejecting nozzles 106 intensively
collides against the source material flame before colliding the deposited body at
the focal position, to actively accelerate the mixing and reaction of the flammable
gas, combustion assisting gas and glass particles. Thus, the deposition efficiency
can be enhanced.
[0027] The adjustment of the focal length L
1 of the small diameter ejecting nozzles 106 is difficult during the deposition. Therefore,
the adjustment of the relation between L
1 and L
2 can be practiced by adjusting the distance L
2 from the burner tip to the deposition plane. Specifically, from the early stage to
the latter half of the deposition, by allowing the burner 100 to move smoothly off
the deposition plane to increase the distance L
2, it is possible to make L
1 < L
2 and to continue the deposition in a stable state, without generating rapid density
variation of the deposited preform.
[0028] Hereinafter, embodiments of the present invention will be described in more detail
while referring to Examples and Comparative Examples, but the present invention is
not limited to these. (Example 1:)
[0029] Using an apparatus as shown in Fig. 1 and by an OVD method, glass particles were
deposited on a starting material. The starting material was formed by welding a dummy
rod with an outer diameter of 50 mm to both ends of a core rod 1. The core rod 1 also
had an outer diameter of 50 mm and a length of 2000 mm. The particles were deposited
by the burner 100 having a concentric fivefold tube structure as shown in Figs. 2A
and 2B, so as to fabricate an optical fiber preform.
[0030] The burner 100 comprises a first tube 101 arranged at the center of the burner 100
to form a glass raw material gas-ejecting port 101P; a second tube 102 arranged outside
the first tube 101 to form a seal gas-ejecting port 102P for ejecting a seal gas;
and a third tube 103 arranged further outside the second tube 102 to form a flammable
gas-ejecting port 103P for ejecting a flammable gas. The burner 100 also includes
eight small diameter combustion assisting gas-ejecting port nozzles 106 contained
in the flammable gas-ejecting port 103P between the second tube 102 and the third
tube 103. The nozzles 106 are arranged on a concentric circle relative to the central
glass raw material gas-ejecting port 101P in a line at equi-distant intervals, so
as to form a small diameter combustion assisting gas-ejecting ports 106P for ejecting
a combustion assisting gas and having a focal length L
1 = 150 mm. That is, the nozzles 106P are arranged in a concentric fashion in such
a way that the respective axes of the nozzles 106 focus at one point by bending the
nozzles 106 as shown in Figs. 2A and 2B. The burner 100 further includes a fourth
tube 104 arranged outside the third tube 103 to form a seal gas-ejecting port 104P
for ejecting a seal gas and a fifth tube 105 arranged outside the fourth tube 104
to form a combustion assisting gas-ejecting port 105P for ejecting a combustion assisting
gas.
[0031] From the start of deposition to the end of the deposition, the respective gases were
fed within respective ranges set forth below with feed rates of the gases gradually
increased. That is, SiCl
4 was fed at 1.0 to 10 L/min as a glass raw material gas and 5 to 20 L/min of a combustion
assisting gas O
2 was also fed to the first tube 101 of the burner; 4 to 6 L/min of a seal gas N
2 was fed to the second tube 102; 70 to 170 L/min of a flammable gas H
2 was fed to the third tube 103; 4 to 6 L/min of a seal gas N
2 was fed to the fourth tube 104; 20 to 50 L/min of a combustion assisting gas O
2 was fed to the fifth tube 105; and a further 5 to 20 L/min of O
2 as a combustion assisting gas was fed to a primary tube (not shown), from which the
small diameter ejecting port nozzles 106 provided in the third tube 103 were branched
off. One hundred (100) kg of glass particles were deposited on the starting material.
The type and feed amount of the gas fed to the respective tubes of the burner are
collectively listed in Table 1, including those in Comparative Examples 1 and 2.
[0032] The deposition was started with the focal length of a plurality of small diameter
ejecting ports 106P set to L
1 = 150 mm and the distance up to a deposition plane 107 set to L
2 = 125 mm. The burner was gradually moved away from the deposition plane as the deposited
body is growing, so that L
1 was equal to L
2 at around the time that the diameter of the deposited body was 150 mm, which was
substantially three times the diameter of the starting material, and L
2 was equal to 175 mm at the end of the deposition. Deposition rates with respect to
representative values of deposition weight obtained as deposition results in Example
1 are collectively listed in Table 2, including results in Comparative Examples 1
and 2. Here, deposition efficiency of Example 1 and Comparative Examples 1 and 2 were
64.o %, 60.9 % and 56.9 %, respectively. Further, average deposition rates for every
5 kg of the deposition weight are shown in Fig. 4. From Fig. 4, it is recognized that
the deposition rate in Example 1 is, during the deposition, superior to that in Comparative
Examples 1 and 2 to be described later.
[Table 1]
| |
TYPE OF GAS |
FLOW AMOUNT (L/min) |
| FIRST TUBE 101 (glass raw material gas-ejecting port) |
SiCl4 |
to 10 |
| O2 |
5 to 20 |
| SECOND TUBE 102 (seal gas-ejecting port) |
SEAL GAS (N2) |
4 to 6 |
| THIRD TUBE 103 (flammable gas-ejecting port) |
H2 |
70 to 170 |
| FOURTH TUBE 104 (seal gas-ejecting port) |
SEAL GAS (N2) |
4 to 6 |
| FIFTH TUBE 105 (combustion assisting gas-ejecting port) |
O2 |
20 to 50 |
| SMALL DIAMETER COMBUSTION ASSISTING GAS-EJECTING PORT NOZZLES 106 |
O2 |
5 to 20 |
[Table 2]
| |
EXAMPLE 1 |
COMPARATIVE EXAMPLE 1 |
COMPARATIVE EXAMPLE 2 |
| Deposition weight (kg) |
Distance L2 (mm) |
Deposition rate (g/hr) |
Distance L2 (mm) |
Deposition rate (g/hr) |
Distance L2 (mm) |
Deposition rate (g/hr) |
| 0 |
125 |
850 |
125 |
870 |
175 |
550 |
| 10 |
130 |
1650 |
125 |
1670 |
175 |
1400 |
| 20 |
135 |
2230 |
125 |
2250 |
175 |
2110 |
| 30 |
141 |
2500 |
125 |
2510 |
175 |
2460 |
| 40 |
146 |
2680 |
125 |
2525 |
175 |
2660 |
| 50 |
151 |
2790 |
125 |
2535 |
175 |
2810 |
| 60 |
156 |
2850 |
125 |
2545 |
175 |
2850 |
| 70 |
161 |
2920 |
125 |
2580 |
175 |
2920 |
| 80 |
167 |
2950 |
125 |
2590 |
175 |
2930 |
| 90 |
172 |
2950 |
125 |
2598 |
175 |
2930 |
| 100 |
175 |
2950 |
125 |
2600 |
175 |
2930 |
(Comparative Example 1:)
[0033] One hundred (100) kg of glass particles were deposited on the starting material in
the same way as in Example 1, except for performing the deposition with the focal
length of the small diameter ejecting ports set to L
1 = 150 mm and maintaining the distance up to the deposition plane L
2 = 125 mm. From Fig. 4, the deposition rates were substantially the same as those
in Example 1 at the early stage of the deposition, but were inferior to those in Example
1 during the latter half of the deposition.
(Comparative Example 2)
[0034] One hundred (100) kg of glass particles were deposited on the starting material in
the same way as in Example 1, except for performing the deposition with the focal
length of the small diameter ejecting ports set to L
1 = 150 mm and maintaining the distance up to the deposition plane L
2 = 175 mm.
[0035] From Fig. 4, the deposition rates were inferior to those in Example 1 during the
early stage of the deposition, but were substantially the same as those in Example
1 in the latter half of the deposition.
[0036] According to the present invention, the deposition efficiency of glass particles
is remarkably improved so as to improve the productivity of the porous glass preform.
1. Verfahren zur Herstellung einer Lichtleitfaser-Vorform, umfassend:
Verwenden eines Brenners (100), der eine konzentrische Mehrfachrohr-Struktur aufweist
und mindestens eine Glasausgangsmaterialgas-Ausstoßöffnung (101 P), die am Zentrum
des Brenners (100) angeordnet ist, eine brennbares Gas-Ausstoßöffnung (103P), die
außerhalb der Giasausgangsmaterialgas-Ausstoßöffnung (101 P) angeordnet ist, und eine
Mehrzahl von Verbrennungsunterstützungsgas-Ausstoßöffnungen mit kleinem Durchmesser
(106P) aufweist, die innerhalb der brennbares Gas-Ausstoßöffnung (103P) in mindestens
einer Linie auf konzentrischen Kreisen bezogen auf die Glasausgangsmaterialgas-Ausstoßöffnung
(101P) angeordnet sind, wobei die Mehrzahl von Verbrennungsunterstützungsgas-Ausstoß-öffnungen
mit kleinem Durchmesser (106P), die auf der gleichen Linie angeordnet sind, die gleiche
Brennweite in einer konzentrischen Weise aufweisen, derart, dass die jeweiligen Achsen
der Mehrzahl von Verbrennungsunterstützungsgas-Ausstoßöffnungen mit kleinem Durchmesser
(106P) an einem Punkt fokussiert sind,
Ausstoßen des Glasausgangsmaterials aus der Glasausgangsmaterialgas-Ausstoßöffnung
(101 P),
Ausstoßen eines brennbaren Gases aus der brennbares Gas-Ausstoßöffnung (103P), die
außerhalb der Glasausgangsmaterialgas-Ausstoßöffnung (101 P) angeordnet ist,
Ausstoßen eines Verbrennungsunterstützungsgases aus der Mehrzahl von Verbrennungsunterstützungsgas-Ausstoßöffnungen
mit kleinem Durchmesser (106P),
Hydrolysieren eines Glasausgangsmaterialgases, das aus der Glasausgangsmaterialgas-Ausstoßöffnung
(101 P) ausgestoßen worden ist, zur Bildung von Glasteilchen,
Abscheiden der Glasteilchen auf einem rotierenden Ausgangsmaterial in der radialen
Richtung,
Einstellen des Verhältnisses von L1 und L2 auf L1 > L2 während der frühen Stufe der Abscheidung, wobei die Brennweite der Mehrzahl von Verbrennungsunterstützungsgas-Ausstoßöffnungen
mit kleinem Durchmesser (106P) durch L1 definiert ist und der Abstand von der Spitze der Mehrzahl von Verbrennungsunterstützungsgas-Ausstoßöffnungen
mit kleinem Durchmesser (106P) zu einer Abscheidungsebene (107) der Glasteilchen auf
dem Ausgangsmaterial durch L2 definiert ist, und
Erhöhen von L2 während des Verlaufs der Abscheidung, so dass L2 größer ist als L1 (L1 < L2), wobei die Beziehung L1 < L2 in der zweiten Hälfte der Abscheidung erreicht wird.
2. Verfahren nach Anspruch 1, wobei der Brenner (100) von der Abscheidungsebene (107)
der Glasteilchen auf dem Ausgangsmaterial derart wegbewegt wird, dass der Abstand
L2 größer gemacht wird, wenn die Abscheidungsmenge erhöht wird, so dass der Außendurchmesser
der Vorform derart erhöht wird, dass die Beziehung L1 < L2 erreicht wird.
3. Verfahren nach Anspruch 2, wobei der Brenner (100) von der Abscheidungsebene (107)
der Glasteilchen auf dem Ausgangsmaterial derart wegbewegt wird, dass die Beziehung
L1 = L2 erreicht wird, wenn der Außendurchmesser der Vorform auf im Wesentlichen das Dreifache
des Durchmessers des Ausgangsmaterials zunimmt.