Technical Field
[0001] The present invention relates to a plasma reactor electrode used in an apparatus,
etc., for removing components contained in a smoke exhaust discharged from a factory,
plant, internal combustion engine, etc., and having an adverse effect on an environment.
Background Art
[0002] As conventional methods for reducing emission amounts of CO (carbonmonoxide), HC
(hydrocarbons), NOx (nitrogen oxides), and PM (particulate matter) contained in an
exhaust gas discharged, for example, from an automobile engine and particularly from
a diesel engine, generally, a catalyst (including an SCR) is used for CO, HC, and
NOx, and a DPF (diesel particulate filter) is used for PM. However, with a DPF, as
a collection rate of PM increases, a state of poor flow of exhaust gas, that is, a
state of high exhaust pressure occurs and causes lowering of engine output. To avoid
this, a method of forcibly combusting and removing the accumulated PM by increasing
a temperature of the exhaust gas (forced combustion) is used with a DPF. Because generally
to increase the temperature of the exhaust gas, fuel is intentionally fed to the catalyst
by post injection or injector injection and a reaction heat generated in this process
is used, excess fuel besides that used for engine combustion is necessary and consequently,
degradation of fuel consumption occurs.
[0003] As a system capable of avoiding the above issue seen with DPFs, there is known a
configuration using a plasma reactor in an exhaust gas purifying apparatus including
a catalyst. For example, a plasma reactor described in Patent Document 1 has a plasma
inducer that generates plasma. After putting the plasma in contact with an exhaust
gas, the exhaust gas is passed through a filter to make soot particles, in other words,
the PM in the exhaust gas be retained in the filter and the PM is combusted by the
plasma.
[0004] Meanwhile, there also has been developed an art employing a porous electrode having
a porous structure and exhibiting both an action of generating plasma inside the pores
to combust the PM by the plasma and an action of improving combustion by increasing
a retention time of the PM by detour of the exhaust gas inside the porous structure
and capture of the PM inside the pores (for example, Japanese Patent Application No.
2005-292998 Specification).
Patent Document 1: Japanese Unexamined Patent Application Publication No. 2002-339731
Disclosure of the Invention
Problems to be Solved by the Invention
[0005] When a filter with a porous structure is disposed adj acent an electrode or a porous
electrode having a porous structure is employed as in the abovementioned documents,
although an area of contact with the PM can be increased to facilitate capture of
the PM and combustion of the PM, in a case where the plasma generated by the electrode
does not act adequately on the PM, the PM is not removed and becomes clogged inside
the reactor or is discharged as it is.
[0006] Although to improve the PM capturing performance, use of a filter or porous electrode
of smaller pore diameter, in other words, a higher specific surface area can be considered,
when a porous structure with a shape of high specific surface area is selected, an
issue of increased exhaust pressure of the exhaust gas arises. In addition, the PM
remains captured inside the pores of the filter or the porous electrode, causing clogging
of the filter and further increase of the exhaust pressure.
[0007] An object of the present invention is to provide a plasma reactor electrode capable
of effectively removing PM (particulate matter) while suppressing increase of exhaust
pressure of an exhaust gas.
Means for Solving the Problems
[0008] To achieve the above object, the present invention provides the following. That is,
a plasma reactor electrode according to a first aspect of the present invention is
installed in a plasma reactor, disposed in an exhaust gas flow path through which
an exhaust gas passes, and includes: a first region, having a first specific surface
area (low specific surface area region) ; and a second region, having a second specific
surface area (high specific surface area region) higher than the first specific surface
area.
[0009] Here, the present inventors have confirmed that the lower the specific surface area
of the electrode, the higher the light emission luminance (FIG. 5). In addition, the
present inventors found that the higher the light emission luminance in a process
of plasma generation from the electrode, the greater a difference of PM removal rate
between a plasma generating state and a plasma non-generating state (FIG. 5).
Thus with the plasma reactor electrode according to the first aspect of the present
invention, the low specific surface area region is preferably positioned upstream
the high specific surface area region in the exhaust gas flow path.
[0010] With the plasma reactor electrode with the above configuration, by disposing the
low specific surface area region at the upstream side in the exhaust gas flow path,
a large amount of plasma can be generated at the upstream side, the PM can be captured
reliably by disposing the high specific surface area region of high PM capturing performance
at the downstream side, and the PM can be oxidized, in other words, combusted favorably
by an action of the plasma generated in the high specific surface area region and
the plasma or a plasma-activated exhaust gas component generated at the low specific
surface area region at the upstream side and moving along with the exhaust gas to
the downstream side.
[0011] Here, the present invention is not limited to a mode where the low specific surface
area region and the high specific surface area region are disposed integrally, and
these regions may respectively be separate bodies. Also, the low specific surface
area region and the high specific surface area region may be disposed apart from each
other.
[0012] It has been confirmed that the light emission luminance of the plasma is significantly
high in a region with a specific surface area of no more than 1000m2/m3, and by disposing
the region with the specific surface area of no more than 1000m2/m3 as the low specific
surface area regionpositioned at the upstream side in the exhaust gas flow path, the
plasma exhibiting the high light emission luminance can be made to act on the PM not
only in the low specific surface area region but also in the high specific surface
area region at the downstream side to which the plasma moves along the exhaust gas
flowpath. Aconfiguration is thus realized where the plasma can be made to act favorably
in the high specific surface area capable of adequately capturing the PM.
[0013] A plasma reactor electrode according to a second aspect of the present invention
includes a region having a specific surface area of no more than 1000m2/m3 and region
differing from the aforementioned region and having a specific surface area of no
less than 1000m2/m3.
[0014] With this arrangement, by the region having the specific surface area of no more
than 1000m2/m3, the PM removal performance can be improved effectively by the plasma
exhibiting the high light emission luminance as described above, and by the region
having the specific surface area of no less than 1000m2/m3, the PM capturing performance
can be improved effectively, thereby realizing an electrode enabling capture of the
PM at a high probability while enabling the plasma generated in a state of high light
emission luminance to react with the captured plasma.
[0015] Preferably, a region constituting a porous structure is included to further facilitate
the capture of the PM.
[0016] Furthermore preferably, as a configuration for increasing the light emission luminance
of the plasma, a region, having a structure where a plurality of protrusions, at which
charges concentrate, are formed on a surface, may be included.
Effects of the Invention
[0017] With the first aspect of the present invention including, in the exhaust gas flowpath,
the low specific surface area region and the high specific surface area region, having
the specific surface area higher than the specific surface area of the low specific
surface area region, while capturing the PM at a high probability by significant improvement
of the PM capturing performance by the provision of the high specific surface area
region, increase of the exhaust pressure of the exhaust gas can be suppressed by the
provision of the low specific surface area region.
Also, by disposing the high specific surface area region at the downstream side of
the low specific surface area region in the exhaust gas flow path, a large amount
of plasma can be generated at the upstream side, the PM can be captured reliably by
the high specific surface area region of high PM capturing performance disposed at
the downstream side, and the PM can be oxidized, in other words, combusted favorably
by the action of the plasma, generated in the high specific surface area region, and
the plasma, moving to the downstream side along with the exhaust gas that has passed
through the plasma field generated by the low specific surface area region at the
upstream side.
[0018] With the second aspect of the present invention including the region having the specific
surface area of no more than 1000m2/m3 and the region having the specific surface
area of no less than 1000m2/m3, while capturing the PM at a high probability by significant
improvement of the PM capturing performance by the provision of the region having
the specific surface area of no less than 1000m2/m3, increase of the exhaust pressure
of the exhaust gas can be suppressed by the provision of the region having the specific
surface area of no more than 1000m2/m3.
[0019] A plasma reactor electrode capable of effectively removing PM (particulate matter)
while suppressing increase of an exhaust pressure of an exhaust gas can thus be provided.
Brief Description of the Drawings
[0020]
FIG. 1 is a schematic view of a plasma reactor according to an embodiment of the present
invention.
FIG. 2 is an explanatory diagram of principal portions of the same embodiment.
FIG. 3 is an explanatory diagram of a configuration of an electrode of a modification
example of the same embodiment.
FIG. 4 is an explanatory diagram of a configuration of an electrode of another modification
example of the same embodiment.
FIG. 5 is a diagram of a relationship of a specific surface area of an electrode and
a radiation luminance by plasma.
FIG. 6 is a diagram of a relationship of the specific surface area of the electrode
and a PM removal rate.
FIG. 7 shows photographs taken during plasma light emission from a porous electrode
and a wave foil electrode.
FIG. 8 is a diagram of a relationship of the specific surface area of the electrode,
the PM removal rate, and a maximum exhaust pressure.
Best Modes for Carrying Out the Invention
[0021] An embodiment according to the present invention shall now be described with reference
to the drawings.
[0022] As shown in FIGS. 1 and 2, a plasma reactor P according to the present embodiment
is installed in an exhaust gas flow path H through which an exhaust gas discharged,
for example, from a diesel engine or other internal combustion engine E passes, and
has a structure where electrodes 1 and dielectrics 2 are laminated alternately in
an interior of a casing P1 of the plasma reactor P. The exhaust gas passes through
along a direction indicated by arrows in which the electrodes 1 and the dielectrics
2 extend. In FIG. 2, particulate matter PM, indicated by PM, is illustrated schematically.
[0023] Each dielectric 2 is disposedbetween two of the electrodes 1 as shown in FIG. 2,
and although in the present embodiment, a plate material composed of alumina is employed,
the present invention is not limited by this configuration of the dielectrics 2 and
dielectrics of various shapes may be employed.
[0024] Here, each plasma reactor electrode 1 according to the present embodiment is installed
in the plasma reactor P disposed in the exhaust gas flow path H through which the
exhaust gas passes and is characterized in including at least a low specific surface
area region (first region) 1a positioned at an upstream side in the exhaust gas flow
path H and a high specific surface area region (second region) 1b having a higher
specific surface area than the low specific surface area region 1a.
[0025] The electrode 1 according to the present embodiment is characterized in including
a region in which the specific surface area is no more than 1000m2/m3, that is, the
low specific surface area region 1a having openings of pore diameter no less than
a fixed dimension, and a region in which the specific surface area is no less than
1000m2/m3, that is, the high specific surface area region 1b having openings of pore
diameter no more than the fixed dimension.
The specific surface area can be measured in compliance with ISO 9277.
[0026] A specific configuration of the electrode 1 shall now be described specifically.
[0027] In the present embodiment, the electrode 1 is composed, for example, of nickel or
copper. As shown in FIG. 2, the low specific surface area region 1a and the high specific
surface area region 1b are configured as porous structures. Although unillustrated,
in the present embodiment, the low specific surface area region 1a and the high specific
surface area region 1b are connected, for example, by brazing, and for the connection,
any of various conductive materials having heat resistance may be employed and a method
for connection is not restricted to brazing and any of various existing connection
methods may be employed.
[0028] The electrode 1 has the porous structure shown specifically in FIG. 2 in likewise
manner in both the low specific surface area region 1a and the high specific surface
area region 1b. That is, the respective surfaces have shapes with practically no flat
portions and have a plurality of penetrating pores 10a and 10b penetrating through
at least from one surface to another surface, a plurality of recesses 11a and 11b
that are depressed at the respective surfaces but do not penetrate through, and a
plurality of protrusions 12a and 12b. The respective surfaces have uneven shapes and
have height differences formed across substantially the entireties, and the protrusions
12a and 12b become portions at which charges concentrate when a voltage is applied
to the electrodes 1 and contribute to improving efficiency of plasma discharge. The
recesses 11a and 11b are not necessarily required and may be formed as portions lower
than the protrusions 12a and 12b by the forming of the protrusions 12a and 12b. The
penetrating pores 10a and 10b do not necessarily have to penetrate directly through
from one surface to another surface. It suffices that upon installation in the plasma
reactor P, the exhaust gas can pass through from an upstream side to a downstream
side. In this case, the penetrating pores 10a and 10b do not necessarily have to be
straight and may be bent or branched in a forked or triple forked manner, etc. The
penetrating pores 10a and 10b have, at inner walls thereof, uneven shapes similar
to the shapes of the surfaces, and in recessed portions thereof or between the inner
walls, effectively obstruct movement of the particulate matter PM and other matter
contained in the exhaust gas and in some cases temporarily capture the particulate
matter PM so that a time taken for the particulate matter PM to pass through the electrode
1 exceeds a time required for the plasma to combust the particulate matter.
[0029] As shown in FIG. 2, the low specific surface area region 1a has the specific surface
area no more than 1000m2/m3 and includes the penetrating pores 10a that open at no
less than fixed dimension and is thereby set to make a light emission luminance of
the plasma high and enabled to make the exhaust gas in the low specific surface area
region 1a be activated, that is, have a high energy. In the present embodiment, a
low specific surface area region exhibiting, for example, a specific surface area
of 500m2/m3 and having openings of approximately 1.9mm diameter is employed.
[0030] The specific surface area of the high specific surface area region 1b is set higher
than that of the low specific surface area region 1a to improve the particulate matter
PM capturing performance. In the present embodiment, the high specific surface area
region has, for example, a specific surface area of 1250m2/m3 and has penetrating
pores 10b with openings of approximately 0.9mm diameter. By the specific surface area
being no less than 1000m2/m3 and the openings being no more than a fixed dimension,
an inner diameter or inner dimension of the penetrating pores 10b can be set to a
dimension that makes the penetrating pores 3 in the high specific surface area region
1b particularly difficult to pass through. The particulate matter PM can thereby be
lowered in speed of passage through the penetrating pores 10b and be retained inside
the electrode 1 for no less than a predetermined time in which the particulate matter
PM can be combusted by the plasma. However, because of not being closed alternately
as in a DPF, a pressure loss can be made low. Although the recesses 11b are not limited
in size and shape, a size enabling the particulate matter PM to be adsorbed readily
by a diffusion mechanism is preferable.
[0031] With this configuration, the exhaust gas flows into the penetrating pores 10a of
the low specific surface area region 1a from the upstream side, passes through the
penetrating pores 10a, and moves into the penetratingpores 10b of the high specific
surface area region 1b at the downstream side as shown in FIG. 2.
[0032] When the exhaust gas passes through the electrode 1, substantially all of the particulate
matter PM contained in the exhaust gas flows downstream along the interiors of the
penetrating pores 10a and 10b of the respective electrodes 1 while being impeded in
movement and being detoured by being temporarily captured, etc., in some cases. Each
electrode 1 thus also functions as a filter with respect to the particulate matter
PM. Because carbon particles constitute a main element of the particulate matter PM,
the captured particulate matter PM also functions as a portion of the electrodes 1.
Thus, when a voltage is applied to the electrodes 1, electrons 1 are discharged from
the electrode 1 itself as well as from the captured particulate matter PM and plasma
discharge is thereby started. Thus, even if the particulate matter PM are collected,
the plasma can be generated without lowering of discharge efficiency.
[0033] In particular, because while the plasma is generated in a state of high light emission
luminance from the low specific surface area region 1a having the penetrating pores
10a with openings of 1.9mm diameter so that the specific surface area is no more than
1000m2/m3 to make the exhaust gas inside the plasma reactor P have a high energy so
that a state enabling removal of the particulate matter PM at a high proportion is
attained, the particulate matter PM retention time can be secured reliably by the
high specific surface area region 1b having the penetrating pores 10b with openings
of 0.9mm diameter so that the specific surface area is no less than 1000m2/m3, the
particulate matter PM captured in the penetrating pores 10a and 10b are successively
combusted from surfaces thereof and made small in diameter and finally removed by
being oxidized completely as schematically shown in FIG. 2. The penetrating pores.
10a and 10b thus do not become clogged and even if the exhaust gas is supplied to
the plasma reactor P continuously, the exhaust pressure at the electrode 1 does not
rise. Increase of the exhaust pressure, such as that occurring in a DPF, due to clogging
of the penetrating pores 10a and 10b can thus be prevented, and upon employment in
a diesel engine, degradation of fuel consumption and lowering of output can be prevented
effectively.
As a method for preparing a porous body, a known method, such as a method disclosed
in Japanese Unexamined Patent Application Publication No.
S53-65206, Japanese Unexamined Patent Application Publication No.
S62-263974, or Japanese Unexamined Patent Application Publication No.
H11-217602 may be used.
<Modification Example>
[0034] A modification example related to the present embodiment shall now be described with
reference to FIG. 3. Portions of the present modification example having the same
configuration as those of the embodiment described above shall be provided with the
same symbols and detailed description thereof shall be omitted.
[0035] A plasma reactor electrode A1 according to the modification example of the present
embodiment employs a metal plate A1 having, as the low specific surface area region
1a, a structure with a plurality of cut surfaces A14 formed on a surface as charge-concentrating
protrusions.
[0036] As the metal plate A1, that composed of a metal such as nickel, copper, iron, stainless
steel, tungsten, etc., can be cited as an example. A thickness of the electrode A1
is for example 200×10-6m (meters) and is not limited to this value as long as a strength
adequate for maintaining the substantially wave-like shape mentioned above can be
obtained.
[0037] As shown in FIG. 3, the metal plate A1 includes raised portions A11 and depressed
portions A12 in a continuous, alternating manner in a lateral direction. The metal
plate A1 also has the raised portions A11 and the depressed portions A12 in a continuous,
alternating manner in a longitudinal direction.
Here, the longitudinal direction is a direction in which the exhaust gas flows (direction
indicated by arrows in FIG. 3). Meanwhile, the lateral direction is a direction substantially
orthogonal to the longitudinal direction. The specific surface area of the metal plate
A1 is no more than 1000m2/m3 as in the embodiment described above.
[0038] By the depressed portion A12 continuing alternately between the raised portion A11
and the depressed portion A12 in the longitudinal direction of the metal plate A1,
a plurality of, that is, several cut surfaces A14 exposed toward the longitudinal
direction are formed at the boundaries of the raised portions A11 and the depressed
portions A12 in the same manner as at an end surface A13 of the metal plate A1 in
the longitudinal direction. An opening of 5mm diameter is formed by each cut surface
A14. The cut surfaces A14, which are portions where charges generated upon application
of voltage to the electrode 1 concentrate, may be formed, for example, by cutting
a raised portion A11 that is continuous in the longitudinal direction to depress the
raised portion A11 at predetermined intervals. The present modification example has
a shape where, in the lateral direction, the raised portions A11 and the depressed
portions A12 continue alternately at portions and the raised portions A11 and the
depressed portions A12 are continuous at other portions, and the present invention
includes such a shape, and although not illustrated, the present invention obviously
also includes a structure where raised portions A11 and depressed portions A12 of
the same length continue alternately in the lateral direction.
[0039] Such a metal plate A1 can be manufactured for example by passing a metal plate material
between two rotating bodies, having recesses and protrusions, while pressing the metal
plate material. Thus, by continuously processing metal plate materials of a predetermined
width, the metal plates A1 of the same shape can be manufactured readily, thereby
enabling reduction of manufacturing cost. Moreover, by using a metal plate material
of thinplate thickness as in the first embodiment, lightweightness and reduction of
pressure loss can be achieved.
<Another Modification Example>
[0040] In another modification example, a metal plate B1, having a plurality of charge-concentrating
portions formed by cutting and raising so as to protrude from one surface of a flat
metal plate material, is employed as shown in FIG. 4 as the low specific surface area
region 1a in a manner similar to the above-described modification example. That is,
with the metal plate B1, protrusions B10, each having a triangular pyramidal shape
formed by cutting and raising, are separated at predetermined distances, in other
words, disposed at predetermined pitches in a longitudinal direction and a lateral
direction. The longitudinal direction and the lateral direction are the same as those
of the above-described modification example. As with the above-described embodiment
and modification example, the specific surface area of the metal plate B1 is set to
no more than 1000m2/m3.
[0041] With each protrusion B10, a bottom surface of the triangular pyramidal shape is made
a penetrating pore and side surfaces B11 are formed so as to cover the penetrating
pore. The two side surfaces B11 are separated at a front side in the longitudinal
direction and are joined at a rear side in the longitudinal direction. An opening
B12 of triangular shape is thereby formed at the front side in the longitudinal direction
of the protrusion B10 and a cut surface B13 substantially equal to a plate thickness
of the metal plate material is formed at a periphery of the opening B12. In the present
embodiment, each protrusion B10 is disposed at an intermediate position between protrusions
B10 in a front column so as not to overlap with a protrusion B10 in the front column.
That is, the respective protrusions B10 are positioned so as to be centered at respective
apexes of a triangular network.
[0042] With each protrusion B10, a ridge B14, formed by the respective side surfaces B11,
and an apex B15, positioned above the opening B12, take on sharp shapes, and these,
together with an edge forming the cut surface B13, cause the concentration of charges
to be significant.
[0043] Even with the metal plate B1 of the above configuration, because a plurality of cut
surfaces B13 are disposedprotrudingly, the same effects as those of the above-described
embodiment are exhibited.
[0044] The protrusions B10 do not necessarily have to be disposed at predetermined pitches
and may respectively be positioned randomly or arbitrarily. With the protrusions B10,
although it is easy to manufacture those of the same height when a cutting and raising
process is performed, the protrusions do not necessarily have to be made the same
in height and it suffices that the protrusions have a clear cut surface B13 and a
sharp apex B15.
[0045] As described above, with the electrodes 1 for the plasma reactor P according to the
present embodiment, by including both the low specific surface area region 1a, having
the specific surface area of no more than 1000m2/m3 and openings with the pore diameter
of no less than the fixed dimension and being high in radiation luminance by plasma,
that is, being high in particulate matter PM removal performance by the plasma, and
the high specific surface area region 1b, having the specific surface area of no less
than 1000m2/m3 and openings with the pore diameter of no more than the fixed dimension
and being high in the particulate matter PM capture rate, the particulate matter PM
removal performance by the plasma is made high by activation of the exhaust gas by
the electrodes 1 as a whole and the time in which the particulate matter PM is retained
inside the electrodes 1 and made to react with the plasma can be secured effectively.
Moreover, the exhaust gas containing the particulate matter PM can be retained or
temporarily captured for an adequate time by the high specific surface area region
1b upon the exhaust gas being put in a state of high energy by plasma being generated
at high luminance in the low specific surface area region 1a. The plasma can thus
be made to react favorably at an adequate activity and for an adequate reaction time
with the particulate matter PM.
[0046] Because each electrode 1 includes the low specific surface area region 1a positioned
at the upstream side in the exhaust gas flow path H and the high specific surface
area region 1b positioned at the downstream side and having the specific surface area
higher than that of the low specific surface area region 1a, the plasma is generated
at the state of high light emission luminance at the upstream side, and by disposing
the high specific surface area region 1b of high particulate matter PM passage inhibiting
performance at the downstream side, the particulate matter PM can be oxidized, in
other words, combusted favorably by action of the plasma, generated in the high specific
surface area region 1b, and the plasma, generated at the low specific surface area
region 1a at the upstream side and moving along with the activated exhaust gas to
the downstream side, while securing the particulate matter PM inside the electrode
1 reliably for an adequate time.
[0047] By positioning the region having the specific surface area of no more than 1000m2/m3
at which the radiation luminance by plasma is high in the low specific surface area
region 1a positioned at the upstream side to activate the exhaust gas by the plasma
exhibiting the high light emission luminance and by activating the exhaust gas by
the plasma further while retaining it for a fixed time in the high specific surface
area region 1b at the downstream side when the exhaust gas moves along the exhaust
gas flow path H, the particulate matter PM can be positioned and oxidized/combusted
in the exhaust gas that has been activated for an adequate time. The plasma can thus
be made to act for an adequate time in the state where the exhaust gas is activated
by the plasma in the high specific surface area capable of adequately retaining the
particulate matter PM.
[0048] With the above-described embodiment, because the low specific surface area region
1a and the high specific surface area region 1b are configured as porous structures,
the role of the electrode 1 can be served while retaining or temporarily capturing
the particulate matter PM favorably.
[0049] Furthermore, with the respective modification examples described above, the low specific
surface area region 1a is made to have a structure having the plurality of cut surfaces
A14 or cut surfaces B13, which are charge-concentratingprotrusions, formed on the
surface to make high the light emission luminance of the plasma favorably, readily
activate the exhaust gas, and further improve the particulate matter PM removal performance
by the plasma.
[0050] Although an embodiment of the present invention has been described above, specific
configurations of the respective portions are not limited to those of the above-described
embodiment and various modifications are possible within a range not deviating from
the gist of the present invention.
[0051] For example, although in the embodiment described above, the low specific surface
area region and the high specific surface area region are disposed along the direction
of extension of the exhaust gas flow path, that is, the direction in which the exhaust
gas flows, the low specific surface area region and the high specific surface area
region may instead be disposed in a direction orthogonal to the direction in which
the exhaust gas flows. Specifically, the specific surface areamaybe varied in the
direction orthogonal to the direction of flow of the exhaust gas by respectively laminating
electrodes having mutually different uniform specific surface areas, or the specific
surface area may be varied in the orthogonal direction in a single electrode.
[0052] Furthermore, in consideration that when the exhaust gas flows through the plasma
generator, the exhaust gas tends to concentrate at a central portion in the exhaust
gas flow path, electrodes respectively differing in specific surface area may be positioned
so that the plasma can be generated with priority at the center of the exhaust gas
flow path. Or, electrodes respectively differing in specific surface areamaybepositioned
so that the exhaust gas flows uniformly inside the exhaust gas flow path.
[0053] Although the low specific surface area region and the high specific surface area
region are configured by an electrode having two types of specific surface areas,
the present invention is not limited to this configuration. That is, the electrode
configuration may be constituted of three or more regions having different specific
surface areas and, for example, a structure, with which the specific surface area
increases in multiple steps from the upstream side to the downstream side, may be
employed.
[0054] Besides the above, the specific configurations of the respective portions are not
restricted to those of the embodiment described above and various modifications are
possible within a range not deviating from the gist of the present invention.
Examples
[0055] Although an example according to the present invention shall now be described, the
present invention is not restricted to this example.
1. Plasma radiation luminance measurement test of porous electrodes
[0056] Measurement of the radiation luminance by plasma was performed on porous electrodes
having four types of specific surface areas.
1.1 <Test Materials>
[0057] The following porous electrodes were tested:
#5: Porous electrode having a specific surface area of 500m2/m3 (pore diameter: approximately
1.9mm)
#8: Porous electrode having a specific surface area of 850m2/m3 (pore diameter: approximately
1.3mm)
#12: Porous electrode having a specific surface area of 1250m2/m3 (pore diameter:
approximately 0.9mm)
#58 : Porous electrode having a specific surface area of 5800m2/m3 (pore diameter:
approximately 0.45mm)
1.2 <Test Method>
[0058] Using a high-voltage pulse power supply with a 600Hz primary voltage being set to
100V to 300V, a 600Hz boosted secondary voltage of 2 to 6kV was applied to each electrode
and the light emission luminance upon light emission due to plasma generation was
measured. The power supply for plasma generation is configured of the two stages of
a primary power supply boosting up to 500V DC and a pulse power supply boosting up
to 10kV.
1.3 <Test Results>
[0059] Test results are shown in a graph in FIG. 5. As shown in this figure, it was found
that the lower the specific surface area, in other words, the larger the pore diameter,
the higher the light emission luminance of the plasma. It was found that the radiation
luminance by plasma is especially high with #5 and #8, with which the specific surface
area is no more than 1000m2/m3.
2. PM removal rate measurement test of porous electrodes
[0060] The porous electrodes tested in the plasma radiation luminance measurement test were
subject to a mode evaluation using a dynamometer. The respective PM removal rates
in cases of employing the respective electrodes were measured.
2.1 <Test Materials>
[0061] The same porous electrodes as those tested in the plasma radiation luminance measurement
test of porous electrodes were tested.
2.2 <Test Method>
[0062] In evaluating the PM removal rate in 10- and 15-mode evaluations using the dynamometer,
the high-voltage pulse power supply set to a 600Hz primary voltage of 400V was used
to apply a 600Hz boosted secondary voltage of 8kV to each electrode, and the PM removal
rate during plasma generation (plasma on) and the PM removal rate when the voltage
was not applied (plasma off) were measured respectively.
2.3 <Test Results>
[0063] The test results are shown in a graph in FIG. 6. In the figure, each arrow schematically
indicates a difference between voltage application and non-application states for
the same electrode. As shown in the figure, regardless of application and non-application
of voltage, the PM becomes more readily trapped and the PM removal rate thus tends
to increase as the specific surface area increases. However, the difference of PM
removal rate due to current application in each electrode is higher the lower the
specific surface area, in other words, the higher the light emission luminance in
the plasma radiation luminance measurement test.
[0064] Thus, from these results, it canbe said that the radiation luminance by plasma and
the PM removal rate due to the plasma are highly correlated. That is, it was found
that with #5 and #8, with which the specific surface area is nomore than 1000m2/m3,
the PM removal rate difference between the plasma generating state and the plasma
non-generating state is large and PM removal by plasma can be performed effectively.
It was found that with #12 and #58, with which the specific surface area is no less
than 1000m2/m3, the PM removal rate is especially high.
3. Comparative plasma radiation luminance measurement test between the metal plate
according to the modification example and the porous electrode
3.1 <Test Materials>
[0065] The porous electrode according to FIG. 2 employed as the low specific surface area
region in the embodiment described above and a metal plate having the same configuration
as the metal plate A1 shown in FIG. 3 employed in the modification example of the
embodiment (referred to hereinafter and in the drawing as the "wave foil electrode")
were tested. The wave foil electrode is made to have openings with a diameter of approximately
5mm.
3.2 <Test Method>
[0066] Using the high-voltage pulse power supply with a 600Hz primary voltage set to 100V
to 300V, a 600Hz boosted secondary voltage of 2 to 6kV was applied to each electrode
and the light emission luminance upon light emission due to plasma generation was
measured.
3.3 <Test Results>
[0067] Plasma light emissions by the respective electrodes are shown in photographs in FIG.
7. As indicated at the lower right of each photograph in the figure, whereas the porous
electrode (#5) indicated a relative value of 58.1, the wave foil electrode, having
an even lower specific surface area and larger openings, exhibited a relative value
of 73.3, thus showing that the wave foil electrode is higher in radiation luminance
by plasma.
4. PM removal rate and exhaust pressure measurement test of porous electrodes
[0068] Plasma radiation luminance of three types of electrodes were measured.
4.1 <Test Materials>
[0069] The following porous electrodes were tested:
#5: Porous electrode having a specific surface area of 500m2/m3 (pore diameter: approximately
1.9mm)
#12: Porous electrode having a specific surface area of 1250m2/m3 (pore diameter:
approximately 0.9mm)
#5+#12: Electrode having the porous electrode #5 at the upstream side of the exhaust
gas flow path and the porous electrode #12 at the downstream side (referred to hereinafter
and in the drawing as the "multi-stage electrode.")
4.2 <Test Method>
[0070] In evaluating the PM removal rate and the exhaust pressure in the 10- and 15-mode
evaluations using the dynamometer, the high-voltage pulse power supply set to a 200Hz
primary voltage of 400V was used to apply a 200Hz boosted secondary voltage of 8kV
to each electrode, and the PM removal rate in the state of plasma generation and the
maximum exhaust pressure at the respective electrodes during the mode tests were measured
respectively.
4.3 <Test Results>
[0071] The test results are shown in graphs in FIG. 8. As can be seen from FIG. 8A, the
multi-stage electrode according to the present invention indicated a high removal
rate similar to that of #12. Meanwhile, as can be seen from FIG. 8B, it was found
that the multi-stage electrode according to the present invention, although exhibiting
a maximum exhaust pressure higher than #5, exhibits a significantly lower maximum
exhaust pressure in comparison to #12 that exhibits practically the same PM removal
rate.
These results thus show that with the multi-stage electrode according to the present
invention, increase of the exhaust pressure of the exhaust gas can be suppressed while
maintaining a high PM removal rate.
Industrial Applicability
[0072] The plasma reactor electrode according to the present invention is used in an apparatus,
etc., for removing components contained in a smoke exhaust discharged from a factory,
plant, internal combustion engine, etc., and having an adverse effect on an environment.