TECHNICAL FIELD
The present invention relates to a burner which, when
used to atomize and burn or flame-hydrolyze a liquid
containing a chemical element that forms a solid oxide by
combustion or flame hydrolysis, discourages the deposition and
buildup of solid oxide on the burner proper, in the burner
vicinity and at the interior of the furnace in which
combustion takes place, by virtue of which the burner is
capable of stable and continuous long-term operation and can
efficiently burn or flame-hydrolyze the liquid. The invention
also relates to a combustion furnace equipped with this
burner, and to a process for burning such a liquid using the
same burner.
BACKGROUND ART
Known processes for burning combustible liquids include
methods in which the combustible liquid is either rendered by
a variety of techniques into a mist-like mixture of liquid
droplets and gas or vaporized, then is delivered to an
incinerator and burned; and methods in which the combustible
liquid is mixed with a solid such as sludge, sand or assorted
debris, and burned.
The combustion method involving vaporization with a
vaporizing burner is applicable to fuels having a boiling
point lower than the thermal decomposition temperature, such
as distillate oils (e.g., gasoline, kerosene, gas oil).
However, when applied to liquid fuels having a thermal
decomposition temperature lower than the boiling point, such
as residual oils (e.g., heavy oils, tar), this method gives
rise to carbon deposition and other undesirable effects on
account of thermal decomposition. Combustion involving
mixture of the combustible liquid with a solid material also
has numerous limitations, including the requirement that the
liquid and the solid material form a non-reactive, chemically
stable combination.
As a result, in those cases where the combustible liquid
to be burned contains a chemical element from group 1A other
than hydrogen, group 2A, group 3B, group 4B, group 5B, group
6B, group 7B, group 8, group 1B, group 2B, group 3A, group 4A
other than carbon, group 5A other than nitrogen, or group 6A
other than oxygen and sulfur (which elements are collectively
referred to hereinafter as the "S element") of the CAS version
of the periodic table of the elements (see F. Albert Cotton
and Geoffery Wilkinson: Advanced Inorganic Chemistry (John
Wiley & Sons, Inc., 1988), back cover), and in cases where the
combustible liquid contains high-boiling compounds, inorganic
salts or the like, use is commonly made of a method in which
the combustible liquid is atomized and burned. Atomizing
techniques known to be used in such cases include mechanical
atomization, rotary atomization, twin-fluid atomization, high-intensity
combustion and radiant combustion.
There are known to be reactions whereby, when an S
element-containing compound is burned or hydrolyzed in a
flame, the S element oxidizes to form an oxide fine powder.
Examples of the industrial application of this principle
include methods for producing synthetic quartz glass and metal
oxide powders. These are familiar as flame hydrolysis
processes.
When a combustible liquid containing the above-described
S element-containing compound (referred to hereinafter as an
"S liquid") is burned, undesirable effects such as those
listed below arise due to the formation of the S element
oxide. These effects are especially striking when the
concentration of S element-containing compound is high.
(1) A powder of the S element oxide readily deposits and
builds up on the burner and on furnace walls near the burner. (2) The deposited S element oxide tends to melt and solidify
under exposure to the elevated temperatures near the burner. (3) The deposited and built-up, or melted and solidified, S
element oxide alters the shape of the burner and its vicinity
and blocks the burner opening, destroying flame stability and
even, in the worst case, extinguishing the flame.
Measures that are used to avoid such effects include
diluting the S liquid so as to lower the concentration of S
element oxide in the combustion gas, and changing the type of
burner or the atomization technique.
However, the above dilution approach is ineffective
unless the concentration of S element-containing compound is
greatly reduced. Unfortunately, this has the drawback of
lowering the throughput of the S liquid, in addition to which
treatment cannot be carried without the use of some other
waste product or fuel as the diluting agent.
There is also combustion technology designed specifically
for compounds that form solids when burned. For example, a
number of combustion processes and apparatuses which are
targeted at the use of special material gases such as the
silanes, arsines and phosphines in waste gases discharged from
semiconductor fabrication equipment, and have a construction
that prevents the deposition of combustion products in the
vicinity of the burner, are known to the art (see JP-A 59-279014,
JP-B 62-134414 and JP-B 1-95214) and have been
furnished for practical use. Unfortunately, all this
technology is targeted at the treatment of substances which
are gases, and so the following drawbacks are encountered when
these known processes are used to burn S liquids.
(1) Because the S liquid must be supplied as a vapor, the
process is accompanied by some type of vaporizing operation
such as heating or pressure reduction. The work is thus more
involved and the system more complex and less cost-effective. (2) Treatment is impossible when the thermal decomposition
point is lower than the boiling point or the S liquid contains
a nonvolatile substance. (3) The concentration of S element oxide fine particles within
the furnace interior space or the flame must be held to a low
level, resulting in a low throughput for the apparatus.
In cases where the S liquid is directly atomized and
burned in the combustion space, merely using a liquid burner
manufactured according to the known gas burner construction or
principle described above results in the deposition and
buildup of fine particles of S element oxide on the burner
proper or in the burner vicinity, making it difficult to carry
out combustion with long-term stability. The reason is that
the S element oxide fine particle concentration within the
furnace interior space or the flame differs markedly between
the above-described known burner technology for burning gases
and burners for burning liquids. Specifically, this
concentration is much higher in burners for burning liquids.
That is, there do not currently exist practical
combustion apparatuses and processes which are capable, by
virtue of modifications in the burner design and the method of
atomization, of the continuous combustion with long-term
stability of liquids which form solids such as S element
oxides using a burner capable of burning such liquids while
inhibiting the deposition of such solid products.
In light of these circumstances, it has been necessary to
adopt, in devices for burning S liquids, a method wherein use
is made of a burner similar to common burners which burn other
combustible liquids and combustion is stopped temporarily to
either periodically clean off the S element oxide that has
built up on the burner itself or in the burner vicinity or to
replace the burner, following which the system is re-ignited
and combustion is continued.
Various types of combustion furnaces may be used to burn
S element-containing liquids, including stoker furnaces,
fixed-bed furnaces, rotary-hearth furnaces, multiple-hearth
furnaces, rotary kilns, fluidized-bed furnaces and vertical
cylindrical furnaces. The appropriate type of furnace is
selected according to the presence or absence of solids and
gases which burn at the same time, as well as the properties
and amounts thereof.
However, when an S element which elicits a reaction that
forms the above-described type of oxide fine powder is present
in a high concentration, these known types of combustion
furnaces have the following drawbacks.
(1) the S element oxide readily deposits and builds up on the
inside walls of the furnace. (2) The deposited S element oxide is exposed to elevated
temperatures within the furnace, and thus readily melts and
solidifies. (3) The deposited and built-up, or melted and solidified, S
element oxide alters the shape of the furnace interior, blocks
the opening, and even, in the worst case, extinguishes the
flame.
Hence, when the above-described S element-containing
liquid is burned in a prior-art combustion furnace, as noted
above in connection with prior-art burners, the method
hitherto used has involved temporarily stopping combustion to
periodically clean off the S element oxide that has deposited,
built up and solidified within the furnace and remove the
oxide from the furnace, then re-igniting the furnace and
continuing combustion.
This can be illustrated with a specific example wherein a
liquid containing a silicon compound (referred to hereinafter
as a "silicon liquid") is burned in a vertical cylindrical
furnace equipped with an external-mixing burner comprising a
central tube having a pressure atomizing configuration, an
outer tube which concentrically surrounds the central tube and
supplies air or oxygen, and a flame holder situated in front
of the central tube (which burner is referred to hereinafter
as a "double-tube burner"). In this case, the silicon dioxide
powder begins to deposit onto the surface of the flame holder
and the inside walls of the furnace about 1 to 2 hours after
the start of combustion. The thickness of the powder deposits
gradually increases and the powder sinters, forming a hard,
porous vitreous substance. The vitreous substance stops good
atomization from occurring, reduces the volume of the
combustion chamber and changes the shape of the chamber,
resulting in a loss in flame stability. In the worst case,
this may lead to obstruction of the burner discharge orifices
or the combustion chamber and flame failure.
To deal with this situation in actual furnace operation,
it is necessary, for example, to temporarily halt combustion
about once every 4 to 8 hours by stopping the supply of
silicon liquid and air or oxygen, and draw the burner out of
the furnace to be cleaned or replaced with another burner that
has been readied for use. Alternatively, every 1 to 2 days,
combustion may have to be halted and the furnace interior
cooled, then opened to break up and remove vitreous silicon
dioxide that has deposited, built up and solidified at the
interior. The burner is then re-ignited and combustion is
continued. Such a process is highly laborious.
Reducing the frequency of such cleaning calls not only
for a change in the combustion conditions, such as the ratio
of combustion-supporting gases (e.g., air, oxygen) and the
feed rate of silicon liquid, but also for lowering the
concentration of the silicon-containing compound within the
silicon liquid by using a liquid capable of dilution or
admixture with the silicon liquid (e.g., toluene, xylene,
kerosene) to dilute or mix with the silicon liquid or,
alternatively, for lowering the concentration of silicon-containing
compound within the substance being burned by
burning at the same time a solid material such as sludge,
assorted debris or sawdust. A sufficient concentration
lowering effect requires, as noted above, that the
concentration of the silicon-containing compound be set very
low. The result is an increase in dilution-related work and
in the amount of material fed to the process, and a decline in
the capacity to burn silicon liquid. Clearly, this is not an
economically desirable approach.
DISCLOSURE OF THE INVENTION
It is therefore an object of the present invention to
provide a burner for atomizing and burning S liquid, which
discourages the deposition and buildup of S element oxides on
the burner proper and in the burner vicinity, by virtue of
which the burner is capable of stable and continuous long-term
operation and can efficiently burn or flame-hydrolyze
combustible liquids such as liquid waste products containing S
element-containing compounds. Another object of the invention
is to provide a combustion furnace equipped with the same
burner and a process for burning the foregoing liquid using
the same burner.
To attain the above objects, the invention provides the
burner, combustion furnace and combustion processes described
below.
Burner
A burner which prevents obstruction by combustion
products and has a circularly concentric multi-tube
construction of three or more tubes is characterized by
comprising:
a central tube which emits a liquid containing a chemical
element that forms a solid oxide by combustion or flame
hydrolysis, a first outer tube which is disposed concentrically
outside the central tube and emits a combustion-supporting gas
and/or a non-combustible gas, a second outer tube which is disposed concentrically
outside the first outer tube and emits a combustion-supporting
gas and/or a non-combustible gas, and optionally, a passage which is disposed outside the second outer tube
and supplies a combustion-supporting gas and/or a non-combustible
gas;
wherein the liquid emitted from the central tube is atomized
and burned by the combustion-supporting gases and/or non-combustible
gases supplied from the outer tubes and the
optional passage disposed outside thereof, and the flame
thereby generated is covered by the combustion-supporting
gases and/or non-combustible gases supplied from the outer
tubes and the optional passage disposed outside thereof.
According to a preferred embodiment of the burner, the
chemical element that forms a solid oxide by combustion or
flame hydrolysis is silicon, the velocity of liquid emission
from the central tube is 5 to 250 m/s, the velocity of gas
emission from the first outer tube is 1 to 250 m/s, the
velocity of gas emission from the second outer tube is 1 to
250 m/s, a burner tile is provided outside of the second outer
tube, and the amount of combustion-supporting gases relative
to the substance being burned is 0.5 to 5.0 times the
stoichiometric amount.
Combustion Furnace
A combustion furnace is characterized by comprising the
above-described burner, a mechanism which holds the surface
temperature on an inside wall of the furnace or the surface
temperature of solid oxide deposits on the furnace inside wall
lower than the melting point or sticking temperature of the
solid oxide, and/or a mechanism which can remove solid oxide
deposits from the inside wall of the furnace.
According to a preferred embodiment of the combustion
furnace, the chemical element that forms a solid oxide by
combustion or flame hydrolysis is silicon; the burner is
configured such that the central tube has an atomizing
mechanism at the tip thereof, each outer tube concentrically
surrounding the central tube has a tip that is either coplanar
with the tip of the central tube or projects forward therefrom
and, if necessary, a flame bolder is disposed in front of the
central tube; and the velocity of liquid emission from the
central tube is 5 to 250 m/s, the velocity of gas emission
from the first and second outer tubes is 1 to 250 m/s, and the
amount of combustion-supporting gases relative to the
substance being burned is 0.5 to 5.0 times the stoichiometric
amount.
Preferably, the combustion furnace additionally has a
mechanism that holds the surface temperature on the inside
wall of the furnace at from 200 to 1,000°C and/or a mechanism
that can remove solid oxide deposits from the inside wall of
the furnace.
Combustion Process
First Embodiment:
A combustion process for atomizing and burning or flame-hydrolyzing
within a combustion furnace a liquid containing a
chemical element that forms a solid oxide by combustion or
flame hydrolysis is characterized in that the process uses the
above-described burner and involves emitting the liquid from
the central tube, carrying out combustion with the combustion-supporting
gases and/or non-combustible gases emitted from the
concentric outer tubes disposed outside the central tube and
also emitted from the optional passage disposed outside the
outer tubes; and covering the flame thereby generated with the
combustion-supporting gases and/or non-combustible gases
supplied from the outer tubes and also supplied from the
optional passage disposed outside the outer tubes.
Second Embodiment:
A combustion process for atomizing and burning or flame
hydrolyzing within a combustion furnace a liquid containing a
chemical element that forms a solid oxide by combustion or
flame hydrolysis is characterized in that the process involves
emitting the liquid from a central tube, carrying out
atomization and combustion with combustion-supporting gases
and/or non-combustible gases emitted from outer tubes provided
with circular concentricity outside the central tube and also
emitted from an optional passage provided outside the outer
tubes, covering the flame thereby generated with the
combustion-supporting gases and/or non-combustible gases
supplied from the outer tubes and also supplied from the
optional passage provided outside the outer tubes, and
carrying out treatment to hold the surface temperature at an
inside wall of the combustion furnace below the melting point
or sticking temperature of the solid oxide and/or carrying out
treatment to remove solid oxide deposits from the inside wall
of the furnace.
Preferably, in this second embodiment, the chemical
element that forms a solid oxide by combustion or flame
hydrolysis is silicon, and the surface temperature on the
inside wall of the furnace or the surface temperature of solid
oxide deposits on the furnace inside wall is held at from 200
to 1,000°C.
As noted above, the burner of the invention has a flame-generating
burner main body with a multi-tube construction.
The flame formed by atomization of a liquid containing the
above-described S element-containing compound is covered from
the outside with a combustion-supporting gas such as air or
oxygen or with a non-combustible gas such as nitrogen
containing the combustion-supporting gases so as to keep
combustion gases present in the furnace from passing through
and mixing with the flame. This arrangement limits
entrainment of the S element oxide formed in the flame by the
externally circulating flow that arises due to combustion,
making it possible to prevent the S element oxide from
approaching the burner and its vicinity. Because the above
arrangement also serves to keep the edge of the internally
circulating flow away from the tips of the multi-tube
construction, S element oxide that has been entrained by the
internally circulating flow can also be prevented from
approaching the burner and its vicinity. As a result, S
element oxide that forms from combustion or flame hydrolysis
of the above-described liquid can be prevented from depositing
and building up, or melting and solidifying, on or near the
burner.
For example, the burner according to the above preferred
embodiment atomizes and burns as fine droplets the S liquid
emitted from the central tube with a combustion-supporting gas
such as air or oxygen emitted from the first outer tube. The
flame that emerges at that time is covered by a combustion-supporting
gas such as air or oxygen, or a non-combustible gas
containing the combustion-supporting gas, that has been
emitted from the second or a subsequent outer tube. By
additionally passing a combustion-supporting gas such as air
or oxygen or a non-combustible gas through a gap between the
second or subsequent outer tube and a burner tile disposed on
the outside thereof, the overall flame is effectively covered
by gas streams. Because the flame is covered by the
combustion-supporting gas such as air or oxygen, or the non-combustible
gas such as nitrogen, that has been emitted from
the gap between the second or subsequent outer tube and the
burner tile, the flame is shielded from circulation and
mixture with combustion gases present within the combustion
furnace. Thus, most of the S element oxide formed in the
flame is discharged into the furnace by the flame jet, so that
entrainment by the externally circulating flow is suppressed,
making it possible to greatly dilute the concentration of S
element oxide in the externally circulating flow and
internally circulating flow. These principles serve to
minimize the concentration of S element oxides within gases
near the burner main body and near the furnace walls in the
burner vicinity, effectively suppressing deposition onto the
solid wall surfaces. Furthermore, because the vicinity of the
central tube tip is covered with a stream of air, oxygen,
nitrogen or the like emitted from a second or subsequent outer
tube, the small amount of S element oxide that has been
entrained by the internally circulating flow never reaches the
vicinity of the atomizing orifice on the central tube, making
it possible to prevent deposition of the S element oxide.
The inventive burner thus resists the deposition and
build up, of S element oxides on the burner itself and in its
vicinity, enabling stable and continuous operation for an
extended period of time, and in turn making it possible to
efficiently burn liquids such as waste products containing S
element-bearing compounds.
Moreover, by using the above-described burner in the
combustion furnace of the invention, as noted above, the
concentration of S element oxides in gases near the burner
itself and near the furnace walls in the burner vicinity is
minimized, effectively suppressing deposition on solid wall
surfaces. Also, when the furnace is equipped with a flame
holder, the small amount of S element oxide entrained by the
internally circulating flow lightly deposits on the surface of
the flame bolder and never reaches the vicinity of the
atomizing orifice at the tip portion of the central tube
positioned behind the flame holder, and so no change occurs in
the atomizing state, making it possible to maintain good
atomization. Moreover, given that the S element oxide which
has deposited on the surface of the flame holder is cooled by
the combustion-supporting gas such as air or oxygen or the
non-combustible gas such as nitrogen that is emitted from the
first outer tube, it does not reach a temperature at which
melting and solidification take place. Hence, the deposits
thicken while remaining in the form of a powder, and stable
combustion is not hindered by the flaking off of vitrified
deposits.
The combustion furnace according to the above-described
preferred embodiment has a mechanism which holds the
temperature of the furnace inside walls lower than the
temperature at which the S element oxide fuses or sticks,
preventing the melting and solidification of any S element
oxide powder formed by combustion that has deposited on the
inside walls, and keeping such deposits in an easy-to-remove
state. In addition, the above furnace also has a mechanism
for removing powder deposits from the wall surface and
enabling such deposits to be taken out of the combustion
system. This makes it possible to prevent the buildup of S
element oxide powder on the inside walls of the furnace, so
that stable and continuous combustion can be achieved.
A specific example of an effective mechanism for holding
the temperature on the inside walls of the furnace within a
required range is a method that involves spraying water within
the combustion chamber. Other suitable methods that may be
used for this purpose include cooling the walls by means of
coolant circulation in a water-cooled wall construction, for
example; and supplying cooling air.
Effective methods for removing powder from the inside
walls of the furnace include the installation of a movable
scraper or soot blowers within the furnace.
Accordingly, the combustion furnace of the invention
discourages the deposition and buildup of solid oxides on or
in the vicinity of the burner, is able to maintain solid
oxides which deposit on the furnace inside walls in an easy-to-remove
state that enables such deposits to be taken out of
the system, and can efficiently burn liquids such as S
element-containing waste products.
That is, as noted above, every type of burner and
combustion furnace that has been used to date for burning
combustible liquids, regardless of differences in the
particular techniques employed, has been designed and
developed for fuels, such as fuel oils (e.g., kerosene, heavy
oils), which generate little or no solids from combustion,
other than soot from incomplete combustion and products
originating from trace amounts of inadvertent impurities in
the fuel. Hence, such prior-art burners and combustion
furnaces are not adapted for burning substances such as S
liquids that generate a large amount (depending on the
composition of the S liquid, at least 50% by weight of the
material burned) of solids by combustion or flame hydrolysis.
To cite a specific example, when silicon liquid is burned
using a double-tube burner and a vertical cylindrical furnace
like those described above, silicon dioxide formed in the
flame is entrained by the externally recirculating flow that
arises near the flame and the internally recirculating flow
that arises at the flame interior, and readily approaches the
solid wall that extends from the vicinity of the burner
discharge orifices to the furnace interior. Because the
silicon dioxide formed by combustion at this time has strong
cohesive and adhesive forces, it readily deposits and builds
up on solid wall surfaces. In addition, the burner vicinity
and the furnace walls are exposed to elevated temperatures due
to the influence of radiant heat, for example, causing the
silicon dioxide powder to sinter, melt and solidify, often
forming hard, porous, and strongly adhering vitreous deposits.
Even in cases where use is made of a burner that employs
another type of atomization, such as rotary or pressure
atomization, entrainment of the silicon dioxide by the
externally recirculating flow and the internally recirculating
flow occurs in much the same way as in a double-tube burner,
resulting in the deposition and buildup or fast adherence of
silicon dioxide to the burner and solid walls extending from
the burner vicinity to the furnace interior.
Also, regardless of which combustion technique is
employed, it is common to place a flame holder on the furnace
interior side in front of the burner discharge orifice or to
position a burner tile so as to surround the burner within the
furnace. However, because the edge of the internally
recirculating flow passes through an area very close to the
flame holder or burner tile, even if the discharge orifice is
protected, silicon dioxide deposition and buildup or melting
and solidification end up occurring on the flame holder or
burner tile. Nor has it been possible in this way to prevent
silicon dioxide deposition on the interior walls of the
furnace.
By contrast, when a combustible liquid containing a
silicon-bearing compound is burned using the burner of the
present invention, no silicon dioxide deposition and buildup
whatsoever occurs on the burner even after 1,000 hours have
elapsed following the start of combustion, enabling combustion
to be continued with full stability. This eliminates both the
need to temporarily halt combustion for cleaning and the labor
involved in dilution to lower the frequency of such cleaning,
thereby resolving the above-described undesirable effects
associated with the combustion of silicon-containing compounds
and enabling dramatic improvements in the operational ease and
cost-effectiveness of the process.
Thus, when a liquid containing an element that forms a
solid oxide by combustion is atomized and burned or flame
hydrolyzed according to the present invention, the solid oxide
does not readily deposit and build up on the burner itself, in
the burner vicinity or inside the combustion furnace, thereby
enabling stable and continuous long-term operation and making
it possible to efficiently burn combustible liquids such as
waste products containing silicon-bearing compounds.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic view showing one embodiment of the
burner according to the present invention.
FIG. 2 is a perspective view showing the main features of
the same embodiment.
FIG. 3 is a partially cutaway, enlarged plan view of area
A of the burner in FIG. 1.
FIG. 4 is a partially cutaway, plan view of another
embodiment of the burner used in the invention.
FIG. 5 is a perspective view of a flame holder in the
embodiment shown in FIG. 4.
FIG. 6 is a schematic view showing an embodiment of a
combustion furnace according to the invention.
BEST MODE FOR CARRYING OUT THE INVENTION
The invention is described more fully below in
conjunction with the accompanying drawings with particular
reference to the combustion of a liquid containing a silicon
liquid. The invention provides a burner for the combustion of
silicon-containing compounds that atomizes as liquid droplets,
then burns or flame-hydrolyzes, a silicon-bearing compound-containing
combustible liquid within a combustion furnace.
The flame-generating burner main body has a circularly
concentric multi-tube construction of at least three tubes
comprising a central tube which emits a combustible liquid
containing a silicon-bearing compound, and two or more outer
tubes disposed concentrically outside the central tube which
emit a combustion-supporting gas and/or a non-combustible gas.
The burner is constructed such that the flame discharged from
the central tube is covered by the gas jets emitted from the
outer tubes, thereby restricting circulation and admixture of
the flame with combustion gases within the furnace.
Combustible liquids that may be furnished for combustion
herein include organic silicon compounds such as liquid
silanes (e.g., tetramethoxysilane), siloxanes (e.g.,
hexamethyldisiloxane) or silazanes (e.g.,
hexamethyldisllazane), and silicone varnishes containing these
liquid organic silicon compounds. Specific examples of
liquids that may be furnished for combustion include silicone
production equipment wash fluids, and distillation fractions
and residues from silicone production.
Suitable examples of the combustion-supporting gas
emitted from the outer tubes include air and oxygen. In the
present case, dry air or oxygen is preferably emitted from the
first outer tube concentrically surrounding the central tube
which emits the above combustible liquid. Dry air or oxygen
may also be emitted from the second outer tube surrounding the
first outer tube, although the emission of ordinary air that
has not been subjected to a drying operation suffices. In the
present invention, there may be disposed outside of the second
outer tube, with circular concentricity thereto, a third or
yet additional outer tubes from which exits a combustion-supporting
gas similar to that emitted from the second outer
tube.
In addition, a burner tile may be disposed at a
predetermined interval outside of the outer tubes so as to
surround the outermost tube. A combustion-supporting gas such
as air or oxygen may be emitted between the outermost tube and
the burner tile.
A non-combustible gas such as nitrogen may be emitted
together with, or even in place of, the combustion-supporting
gas.
In a mechanical atomizing burner, the first outer tube
preferably emits a combustion-supporting gas such as air or
oxygen, and the second outer tube preferably emits a
combustion-supporting gas or a non-combustible gas containing
a combustion-supporting gas, although in some cases it may
emit only a non-combustible gas.
In a twin-fluid atomizing burner, it is preferable for
both the first and second outer tubes to emit a combustion-supporting
gas or a non-combustible gas containing a
combustion-supporting gas.
The velocity of gas emission from the first and second
outer tubes is preferably from 1 to 250 m/s.
If a twin-fluid atomizing burner is employed, the
velocity of gas emission from between the outermost tube and
the burner tile is preferably from 5 to 100 m/s when air is
used as the gas.
Any suitable technique may be used for atomizing the
liquid in the central tube of the multi-tube burner, provided
it has a mechanism for mixing the liquid with a gas to obtain
a mist-like mixture of liquid droplets and gas. Examples of
atomizing techniques that may be used include mechanical
atomization, rotary atomization and twin-fluid atomization.
As is apparent from the above-described operative
principle of the invention, in the present case, a silicon
liquid is emitted from the central tube in the multi-tube
burner, and the flame generated at this time must be covered
by the jets of gas discharged from the outer tubes. When the
silicon liquid is discharged from somewhere other than the
central tube, such as from the first or second outer tube, the
operative principle does not apply, and so the silicon dioxide
formed by combustion readily deposits in the vicinity of the
discharge orifices, making the burner unfit for practical use.
FIGS. 1 to 3 illustrate a specific embodiment of a burner
according to the present invention in which the central tube
for discharging a liquid is of an external-mixing twin-fluid
atomizing configuration. The burner has a main body
comprising a liquid-emitting central tube 1 in combination
with first and second combustion-supporting gas and/or non-combustible
gas-emitting outer tubes 2 and 3 disposed with
circular concentricity outside of the central tube 1. The tip
of the central tube 1 projects out beyond the tip of the
inside outer tube 2, and the tip of the inside outer tube 2
projects out beyond the tip of the outside outer tube 3. The
combustible liquid, the combustion-supporting gas such as air
or oxygen, and/or the non-combustible gas such as nitrogen are
each supplied to central tube 1 and outer tubes 2 and 3 from
fluid feed ports 5.
The burner has a burner tile 4 disposed such as to
surround the outside of the outermost tube 3. The tip of the
burner main body is situated short of the face of the burner
tile on the furnace interior side thereof. In this burner,
air or the like is fed from an air inlet 8 to a flow passage 7
(between the burner tile 4 and the second outer tube 3) having
a windbox 6.
Referring to FIG. 3, which is a schematic partially
cutaway view showing the tip portion of the multi-tube
arrangement in the burner shown in FIG. 1, a combustible
liquid passage 9 is formed within the central tube 1, and gas
passages 10 and 11 are formed respectively in outer tubes 2
and 3.
The inventive burner depicted in FIGS. 1 to 3 has the
following construction.
(1) The tubes making up the multi-tube arrangement are each
disposed such that their respective tips are circularly
concentric. (2) The tips of each outer tube surrounding the atomizing area
are preferably situated such that either the tip of the
outside tube is stepped back from the tip of the inside tube,
or the tip of each outer tube is coplanar with the tip of the
atomizing region. (3) Preferably, the tip portion of each tube is shaped such as
to taper toward the tip, has a straight cylindrical shape or
has a shape representing a combination thereof; that is, the
shape is preferably not one which flares out toward the tip. (4) The burner tile preferably has a shape which widens toward
the inside of the combustion furnace, has parallel sides, or
is a combination thereof. (5) The tip portion of each tube preferably has a wall
thickness which decreases toward the tip at an acute angle,
remains constant, or has a shape that represents a combination
thereof; that is, the wall thickness preferably does not
increase toward the tip. (6) The tip of the multi-tube arrangement is preferably
situated such as to be either short of or coplanar with the
face of the burner tile on the combustion furnace side; that
is, it should preferably not jut out into the furnace.
In the practice of the invention, given the operative
principle described earlier, it is preferable for the flow
rate of combustion-supporting gas and non-combustible gas for
covering the flame to be within a suitable range which is at
least sufficient to shield the flame from combustion gases
present within the combustion furnace, yet is not so excessive
as to hinder combustion. Of course, to continuously maintain
the flame and assure good combustion, it is necessary to feed
the minimal amount of oxygen (stoichiometric amount) necessary
for complete combustion of the combustible liquid.
Moreover, to suppress deposition of the S element oxide
on the burner, in the burner vicinity, and especially near the
discharge orifice, it is preferable for the velocity of the
fluid emitted from each tube in the multi-tube arrangement to
be regulated within a range in velocity which is at least
sufficient to maintain good atomization yet not so excessive
as to hinder combustion.
Specifically, the velocity of liquid emission from the
central tube is preferably set at from 5 to 250 m/s, the
velocity of gas emission from the first outer tube is
preferably set at from 1 to 250 m/s, the velocity of gas
emission from the second outer tube is preferably set at from
1 to 250 m/s, and the velocity of gas emission from between
the outermost tube and the burner tile when air is used as the
gas is preferably set at from 5 to 100 m/s. Also, the amount
of combustion-supporting gas supplied between the outer tubes
and the burner tile, relative to the substance being burned
that is emitted from the central tube, is preferably 0.5 to
5.0 times the stoichiometric amount.
When combustion is carried out using the burner described
above, the liquid is atomized by being emitted at the above-indicated
velocity and a temperature and pressure below the
boiling point and by emission of the combustion-supporting gas
and/or non-combustible gas from the first outer tube at the
above-indicated velocity and a temperature of 0 to 30°C. The
resulting atomized mixture is burned, and the flame thus
generated is covered, with the combustion-supporting gas
and/or non-combustible gas emitted from the second and
subsequent outer tubes and also from between the burner tile
and the outermost tube. The temperature of the combustion-supporting
gas and/or non-combustible gas emitted from the
second and subsequent outer tubes and from between the burner
tile and the outermost tube is preferably from 0 to 30°C.
A plurality of burners having the construction of the
invention may be installed at the interior of a single burner
tile. Moreover, the burner tile may be preheated to improve
the fluidity of the combustible liquid and of the combustion-supporting
gas and non-combustible gas supplied to the burner,
as well as for other reasons, such as controlling combustion.
The combustion furnace of the invention has a cooling
mechanism for maintaining the temperature at the inside walls
thereof within a required range, and also has a mechanism for
removing and eliminating solids that have deposited on the
inside walls. This arrangement has a two-fold purpose. When
the oxide that has formed from combustion at the above-described
burner has deposited as a powder on the inside walls
of the furnace, the oxide powder is kept at a temperature
lower than its sintering temperature or melting point so as to
maintain the powder in an easy-to-remove state. In addition,
periodic operation of the removal mechanism serves to remove
such deposits from the system while still in the form of a
powder.
One effective mechanism for keeping the temperature of
the furnace inside wall within the required range is to spray
the inside of the furnace with water. Other methods that may
be used to achieve the same end include the use of a furnace
wall having a coolant-circulating construction such as a
water-cooled wall, and methods involving the supply of cold
air. One effective deposit-removing mechanism is a soot
blower. Other methods that may be used include installing a
movable scraper within the furnace, and passing spheres made
of a heat-resistant material such as iron or ceramic along the
inside surface of the furnace walls.
When burning silicon-containing compounds, for example,
the surface temperature at the inside wall of the furnace is
preferably held within a range of 200 to 1,000°C. To achieve
complete combustion, a temperature of at least 500°C at which
spontaneous ignition of organic materials occurs is preferred.
To completely prevent sintering of the silicon dioxide powder,
it is preferable to set the temperature at not higher than
850°C, at which crystal modification from quartz to tridymite
can be prevented.
The burner in the combustion furnace of the invention may
be an external-mixing twin-fluid atomizing burner like that
shown in FIGS. 1 to 3, although use of the burner shown in
FIG. 4 is also possible. FIG. 4 illustrates a burner
according to the present invention in which the liquid
emitting central tube has a pressure atomizing configuration,
and the flame-generating burner main body has a circularly
concentric multi-tube construction composed of three tubes.
This burner main body has a liquid-emitting central tube 21,
and first and second outer tubes 22 and 23, each of which
emits a combustion-supporting gas or a combustion-supporting
gas-containing non-combustible gas and is disposed
concentrically outside of the central tube 21. A liquid is
supplied to the central tube 21 from a combustible liquid feed
port 14, and a combustion-supporting gas such as air or oxygen
and/or a non-combustible gas such as nitrogen are supplied to
the first and second outer tubes 22 and 23 from respective gas
feed ports 15 and 16. A flame holder 17 is disposed inside
the tip portion of the first outer tube 22 so as to be
positioned in front of the central tube 21. The flame holder
17, as shown in FIG. 5, is shaped as a conical plate having an
opening 17a at the center. If necessary, the plate may bear a
plurality of holes, or may have a plurality of blades or
projections thereon. The atomized mixture emitted from behind
the flame holder 17 must pass through the opening 17a and
emerge in front of the flame holder 17.
The pressure-atomizing burner of the invention shown in
FIG. 4 has the following construction.
(1) Each tube in the multi-tube construction is disposed so
that the respective tips are circularly concentric. (2) Preferably, the tips of the respective tubes in the multi-tube
construction are arranged such that outside tubes project
further forward (in the direction of emission) than inside
tubes, or the tips of the respective outer tubes are coplanar
with the tip of the central tube. (3) Preferably, the tip portion of each tube is shaped such as
to taper toward the tip, has a straight cylindrical shape or
has a shape representing a combination thereof; that is, the
shape is preferably not one which flares out toward the tip. (4) Preferably, the flame holder 17 is disposed forward of the
central tube and at the interior of the outer tube tips,
although it is possible not to include a flame holder if the
flame has a high stability owing to such factors as the nature
of the substance being burned and the furnace operating
conditions. (5) The tip portion of each tube preferably has a wall
thickness which decreases toward the tip at an acute angle,
remains constant, or has a shape that represents a combination
thereof; that is, the wall thickness preferably does not
increase toward the tip.
In this case as well, given the operative principle
described above, it is preferable for the flow rate of
combustion-supporting gas and/or non-combustible gas for
covering the flame to be within a suitable range which is at
least sufficient to shield the flame from combustion gases
present within the combustion furnace, yet is not so excessive
as to hinder combustion. Of course, to continuously maintain
the flame and assure good combustion, it is necessary to feed
the minimal amount of oxygen (stoichiometric amount) necessary
for complete combustion of the combustible liquid.
Moreover, to suppress deposition of the S element oxide
on the burner, in the burner vicinity, and especially near the
discharge orifice, it is preferable for the velocity of the
fluid emitted from each tube in the multi-tube arrangement to
be regulated within, a range in velocity which is at least
sufficient to maintain good atomization yet not so excessive
as to hinder combustion.
Specifically, the velocity of combustible liquid emission
from the central tube is preferably set at from 5 to 250 m/s,
and especially from 5 to 50 m/s in the case of pressure
atomization. The velocity of gas emission from the first and
second outer tubes is preferably set at from 5 to 50 m/s when
air is used in a pressure-atomizing burner.
The amount of combustion-supporting gas supplied between
the outer tubes and the burner tile, relative to the substance
being burned that is emitted from the central tube, is
preferably 0.5 to 5.0 times the stoichiometric amount. To
hold the flame stable, it is even more preferable to set the
amount of combustion-supporting agent at from 0.8 to 2.0 times
the stoichiometric amount.
When combustion is carried out using the burner described
above, the liquid is atomized by being emitted at the above-indicated
velocity and a temperature and pressure below the
boiling point and by emission of the combustion-supporting gas
and/or non-combustible gas from the first outer tube at the
above-indicated velocity and a temperature of 0 to 30°C. The
resulting atomized mixture is burned, and the flame thus
generated is covered, with the combustion-supporting gas
and/or non-combustible gas emitted from the second and
subsequent outer tubes and also from between the burner tile
and the outermost tube. The temperature of the combustion-supporting
gas and/or non-combustible gas emitted from the
second and subsequent outer tubes and from between the burner
tile and the outermost tube is preferably from 0 to 30°C.
A plurality of burners having the construction of the
invention may be installed at the interior of a single burner
tile. Moreover, the burner tile may be preheated to improve
the fluidity of the combustible liquid and of the combustion-supporting
gas and non-combustible gas supplied to the burner,
as well as for other reasons, such as controlling combustion.
FIG. 6 illustrates an embodiment of a combustion furnace
according to the present invention, and specifically a
vertical cylindrical furnace having at the top a pressure-atomizing
three-tube burner, a water-spraying nozzle for
temperature regulation, and a movable scraper driving
mechanism. The furnace is provided in a barrel portion
thereof with soot blowers and a movable scraper. This
combustion furnace has a furnace main body 18 in which there
is disposed at the top thereof a burner like that shown in
FIG. 4 comprising a central tube 21 and outer tubes 22 and 23.
The burner supplies and ignites an S liquid and a combustion-supporting
gas such as air or oxygen, thereby burning the S
liquid and forming a solid oxide within the furnace main body
18. The furnace main body 18 is provided on a sidewall
thereof with a water-spraying nozzle 19 for cooling. The
nozzle 19 sprays water to allow combustion to continue while
keeping the combustion temperature in the furnace main body 18
within a range where the S element oxide does not melt or
sinter. In addition, soot blowers 24 are installed at
suitable positions on the sidewall of the furnace main body 18
where S element oxide powder formed by combustion deposits and
builds up. The soot blowers 24 are periodically operated at
fixed intervals of time to knock down S element oxide powder
from the furnace wall. The knocked down powder is discharged
together with combustion gases from an exhaust opening 25 at
the bottom of the furnace main body 18.
An annular movable scraper 26 is normally situated within
the furnace main body 18 at the top thereof. The scraper 26
is coupled by a chain 27 to a drive mechanism 28 located
outside of the furnace main body 18. Operation of the drive
mechanism 28 causes the chain 27 to wind onto or play out from
the drive mechanism 28, causing the scraper 26 to slide upward
or downward along the inner peripheral wall surface of the
furnace main body 18 so as to knock down any S element oxide
powder that has deposited and built up on the walls of the
furnace main body 18 and has not been removed by the soot
blowers 24.
Although the embodiment of the inventive furnace shown in
FIG. 6 is not provided with a burner tile, and is shaped to
hold the flame using the burner and a flame holder, a burner
tile may be provided in the manner described above.
Temperature control within the illustrated furnace is carried
out by a water spraying system but, as noted earlier, any
suitable mechanism which maintains the inside wall surface at
a temperature at which the S element oxide powder does not
melt or sinter may be used. Illustrative examples include a
direct cooling system such as water-cooled walls, and methods
involving the supply of cold air. Also, even though the use
of both soot blowers and a movable scraper has been described
above as an example of a method for removing S element oxide
from the inside walls, any other suitable method may be used
without particular limitation so long as it is a mechanism
which knocks down such powder from the inside surfaces of the
furnace walls. Illustrative examples include a method in
which heat-resistant spheres are dropped from the top of the
furnace and a method that involves vibrating the entire
furnace.
The type of furnace used in the present embodiment is a
vertical cylindrical furnace which burns only liquids
containing S element-bearing compounds. However, if the
combustion furnace must also be fed other liquids and/or
solids at the same time, use may be made of any suitable type
of furnace, provided this has the mechanisms critical to the
practice of the invention, as noted below.
The combustion furnace of the invention shown in FIG. 6
has a construction which includes the following features.
(1) A mechanism which keeps the temperature at the inside
surface of the furnace wall lower than the melting point or
sintering temperature of the S element oxide powder. (2) A mechanism which removes S element oxide powder that has
deposited and built up on the furnace inside walls, and
discharges such powder from the system.
The following examples and comparative examples are
provided to illustrate the invention, and are not intended to
limit the scope thereof.
EXAMPLE 1
Tetramethoxysilane was burned under the following
conditions using a burner of the construction shown in FIGS. 1
to 3.
(1) Burner Shape
Central tube (stainless steel): bore, 8 mm; bore at discharge
orifice, 4 mm
First outer tube (stainless steel): bore, 20 mm; bore at
discharge orifice, 8 mm
Second outer tube (stainless steel): bore, 32 mm; bore at
discharge orifice, 28 mm
(2) Fluid Emitted from Each Tube, and Emission Rate and
Temperature
Central tube: tetramethoxysilane (200 kg/h), 20°C
First outer tube: air (16 Nm3/h), 20°C
Second outer tube: air (50 Nm3/h), 20°C
Gap between second outer tube and burner tile: air (2,300
Nm3/h), 20°C
(3) Results
When combustion was carried out under the above
conditions, even after 1,000 hours of combustion, growth in
silicon dioxide deposits was not observed at the tips of the
respective tubes, on the inside surface of the burner tile or
on the inside walls of the furnace surrounding the edges of
the burner tile, thereby allowing stable combustion to be
continued.
COMPARATIVE EXAMPLE 1
Tetramethoxysilane combustion was carried out under the
same conditions as in Example 1 using a burner which was
similar but had a two-tube construction without a second outer
tube.
When combustion was carried out under these conditions,
growth in silicon dioxide deposits occurred in the following
areas within 4 hours from the start of combustion:
(a) a region extending from about 2 mm in front to about 20 mm
behind the tip of the multi-tube configuration (b) a region extending from the edge of the burner tile to the
furnace inside walls in the circumferential direction for
about 400 mm, and backwards toward the interior for about
200 mm.
Combustion was continued in spite of this, whereupon
growth in the deposition of silicon dioxide continued. Ten
hours after tile start of combustion, the tip of the multi-tube
burner and the space in front of the burner became obstructed,
as a result of which continuous combustion ceased to be
maintained and the flame went out.
COMPARATIVE EXAMPLE 2
Tetramethoxysilane gas obtained by vaporizing
tetramethoxysilane with an evaporator was burned under the
following conditions using the burner described in Comparative
Example 1.
(1) Fluid Emitted from Each Tube, and Emission Rate and
Temperature
Central tube: gaseous tetramethoxysilane (2.1 kg/h), 130°C
First outer tube: air (1.0 Nm3/h), 20°C
Gap between first outer tube and burner tile: air (17.0
Nm3/h), 20°C
(2) Results
The combustion reaction was carried out under the above
conditions, obtaining similar results as in Example 1.
Silicon dioxide deposition did not occur, making it possible
to continue stable combustion.
EXAMPLE 2
Tetramethoxysilane (Si(OCH3)4) combustion was carried out
under the following conditions using a burner of the
construction shown in FIG. 4.
(1) Burner Shape
Central tube (stainless steel): bore, 4 mm; tip with
pressure-atomizing configuration; bore at discharge orifice,
0.2 mm
First outer tube (stainless steel): bore, 45 mm
Second outer tube (stainless steel): bore, 54 mm
Flame holder (stainless steel): diameter of opening, 10 mm;
outside diameter, 40 mm; central angle in cross-section,
160°
Distance between central tube tip and first outer tube tip:
10 mm
Distance between first outer tube tip and second outer tube
tip: 3 mm
(2) Fluid Emitted from Each Tube, and Emission Rate and
Temperature
Central tube: tetramethoxysilane (1.6 kg/h), 20°C
First outer tube: dry air (14.5 Nm3/h), 20°C
Second outer tube: air (9.7 Nm3/h), 20°C
(3) Furnace Temperature
Top of furnace (300 mm from top end): 850°C
Base of furnace (900 mm from top end): 550°C
(4) Furnace Shape and Other Parameters
Barrel (stainless steel): inside diameter, 208 mm; length,
1,000 mm; wall thickness, 4 mm
Soot blowers (iron): total of 3 blowers, one each positioned
300 mm, 600 mm and 900 mm from top end of furnace
Scraping mechanism (iron): cylindrical, with outside diameter
of 180 mm, height of 30 mm, and plate thickness of 5 mm;
suspended from above by chains and vertically movable
Water-spraying nozzle for cooling (stainless steel): tip is
positioned 200 mm from top end of furnace; has twin-fluid
atomizing configuration at tip for spraying water
Soot blowing interval: every 20 minutes
Scraping interval: every 60 minutes
(5) Results
The following results were obtained from operation under
the above conditions.
a) In the interval from the start of combustion to about 30
minutes, light deposition of silicon dioxide powder occurred
on the burner and in its vicinity ( on the surface of flame
holder, at the tips of the first and second outer tubes (both
having wall thicknesses of 2 mm), and on the outside of the
second outer tube), as well as in the barrel portion of the
furnace about 500 mm from the top of the furnace. b) When furnace operation was continued for another 10 hours,
the silicon dioxide which had deposited on the burner and in
its vicinity flaked off under its own weight above a given
thickness, and deposits on the inside walls of the furnace
were kept from growing above a given thickness by periodic
activation of the soot blowers and scraper. It was thus
possible to maintain good combustion. c) Combustion was stopped after 10 hours, following which the
furnace was taken apart and inspected. The silicon dioxide
inside the furnace retained the properties of a fine powder,
from which it was confirmed that melting and sintering did not
arise.
COMPARATIVE EXAMPLE 3
Tetramethoxysilane combustion was carried out under the
same conditions as in Example 2 using a burner which was
similar but had a two-tube construction without a second outer
tube.
When the combustion reaction was carried out under these
conditions, silicon dioxide powder continued to settle onto
the surface of the flame holder and onto the outside and tip
of the first outer tube for as long as combustion continued.
After about 2 hours, the surface of the flame holder and the
front of the first outer tube became almost entirely
obstructed by silicon dioxide, at which point combustion could
no longer be continued.