Background of the Invention
[Field of the Invention]
The present invention relates to a high-frequency
heating catalyst used in an exhaust gas apparatus for an
internal combustion engine or the like and, particularly,
to a high-frequency heating catalyst for making clean
harmful exhaust gas exhausted at the time of the start of
the engine at low temperatures.
[Description of the Prior Art]
Exhaust gas from a car contains air pollutants such
as hydrocarbon, carbon monoxide and nitrogen oxide. To
make clean such harmful exhaust gas, there are available
an engine combustion system and a post-processing system
using a catalyst. The post-processing system using a
catalyst comprises letting exhaust gas from a car pass
through cleaning means having a three-element catalyst
composed of a precious metal element alloy such as Pd/Rh
or Pt/Rh to oxide hydrocarbon and carbon monoxide and
reduce nitrogen oxide so as to change them into harmless
carbonate gas, vapor and nitrogen and discharging them
from the car.
However, in the exhaust gas apparatus of an internal
combustion engine having a catalyst device of the prior
art, a catalyst is heated by the exhaust gas of the
internal combustion engine. Therefore, it takes time for
the catalyst to reach a temperature at which its catalytic
function can be effectively exerted and the catalyst
cannot remove the above harmful substances completely at
the time of the start of the internal combustion engine at
low temperatures.
To remove harmful substances contained in exhaust gas
even at the time of start at low temperatures, there is
disclosed a method for heating a catalyst in the cleaning
means quickly using a microwave (Japanese Laid-open Patent
Application No. Hei 4-353208). As shown in Fig. 8,
exhaust gas G supplied from a exhaust pipe 21a is let pass
through cleaning means 23A provided in a heating chamber
22 to make clean the exhaust gas G, and then the clean
exhaust gas G is discharged from an exhaust pipe 21b. The
cleaning means 23A is held in the heating chamber 22 by a
supporting member 24. A microwave generated by a high-frequency
oscillator 25 is irradiated onto the cleaning
means 23A through a waveguide path 26. As shown in Figs.
9(a) and 9(b), the cleaning means 23A comprises a
substrate 1 which has a honeycomb structure and is made
from a ceramic material such as alumina which rarely
absorbs a high-frequency wave and a high-frequency heating
catalyst 2A formed on the barrier 1K of the substrate 1
and having a three-element catalyst 2b such as Pd/Rh or
Pt/Rh carried on a high-frequency absorbing material 2a
such as ZnO which absorbs a microwave. The high-frequency
absorbing material 2a converts the energy of the microwave
radiation into heat energy to raise the temperature of the
catalyst 2b to its operation temperature, thereby removing
harmful substances contained in exhaust gas passing
through through holes 1S in the substrate 1.
Figs. 10(a) and 10(b) are diagrams showing the
structure of conventionally used cleaning means 23B which
comprises (1) a substrate 1 composed of an insulating
cordierite sintered body having a honeycomb structure,
insulating properties and high thermal shock resistance
and (2) a high-frequency heating catalyst 2B which
comprises a high-frequency absorbing layer 2c formed on
the surface of each barrier 1K of the substrate 1 and made
from a high-frequency absorbing material and a wash coat
layer 2d formed on the surface of the high-frequency
absorbing layer 2c and carrying Pt/Rh dispersed therein.
The Pt/Rh catalyst is dispersed and carried in the
vicinity of the surface of the wash coat layer 2d. A
microwave irradiated onto the cleaning means 23B is
converted into heat by the above high-frequency absorbing
layer 2c to raise the temperature of Pt/Rh dispersed and
carried in the vicinity of the surface of the wash coat
layer 2d to its operation temperature, whereby harmful
substances contained in the exhaust gas passing through
the cleaning means 23B are removed.
However, since the heat capacity of the wash coat
layer 2d is large in the cleaning means 23B, the power of
the input microwave must be made large to quickly heat
Pt/Rh (catalyst) dispersed and carried in the vicinity of
the surface of the wash coat layer 2d. Meanwhile, in the
cleaning means 23A, since the high-frequency heating
catalyst 2A is a mixture of a high-frequency absorbing
material 2a and a three-element catalyst 2b, the heat
propagation efficiency thereof is higher than that of the
high-frequency heating catalyst 2B. However, since the
characteristic impedance of propagation space which is
determined by the frequency of high-frequency radiation
(microwave) or a medium through which a high frequency
wave propagates is not taken into account in the design of
the impedances of the high- frequency heating catalysts 2A
and 2B, the impedances of the high- frequency heating
catalysts 2A and 2B do not match the characteristic
impedance of the propagation space. Therefore, when the
conventional high- frequency heating catalysts 2A and 2B
are used, a high-frequency wave is reflected on the
surfaces of the high- frequency heating catalysts 2A and
2B, thereby greatly reducing the absorption efficiency of
the high-frequency wave.
To improve the catalytic activity of the conventional
high-frequency heating catalyst 2A which is a mixture of a
high-frequency absorbing material 2a such as ZnO or CoO
and a three-element catalyst 2b, the content of the three-element
catalyst 2b must be increased. However, when the
content of the three-element catalyst is increased, the
heating efficiency of the high-frequency heating catalyst
2A lowers.
Further, since the high- frequency heating catalysts
2A and 2B are carried on the surface or in the interior of
the substrate 1 uniformly and a flow direction of the
exhaust gas G is not taken into account, efficient high-frequency
heating is impossible.
Moreover, when La(1-x)SrxCoO3 containing Co is used as
the high-frequency absorbing material in conjunction with
with the substrate 1 composed of a cordierite sintered
body which is a composite metal oxide essentially composed
of MgO and Al2O3, Al contained in the substrate 1 reacts
with Co contained in the high-frequency absorbing layer 2c
upon a rise in the temperature of the high-frequency
heating catalyst 2B with the result that the composition
ratio of the La(1-x)SrxCoO3 differs from the initial
composition ratio, thereby deteriorating the heat
conversion efficiency of the microwave. As a result, the
temperature elevation rate of the catalyst lowers and the
catalytic function efficiency of the high-frequency
heating catalyst 2B deteriorates. Also when the high-frequency
absorbing material contains Mn like La(1-x)SrxMnO3
and the material forming the substrate 1
contains Si like a composite oxide of SiO2 and MgO, the
same reaction occurs with the result of a reduction in the
catalytic function efficiency of the high-frequency
heating catalyst 2B.
Summary of the Invention
It is therefore an object of the present invention
which has been made in view of the above problems of the
prior art to provide a high-frequency heating catalyst
which can make clean harmful exhaust gas exhausted at the
time of the start of an internal combustion engine at low
temperatures by absorbing a high-frequency wave
effectively to increase the temperature of a catalyst to
its operation temperature at the time of the start at low
temperatures.
According to a first aspect of the present invention,
there is provided a high-frequency heating catalyst which
comprises a high-frequency absorbing layer formed on the
surface of a substrate made from a material which rarely
absorbs a high-frequency wave and made from a high-frequency
absorbing material and a catalyst such as Pd, Pd/Rh or
Pt/Rh, carried by the high-frequency absorbing layer, for
making clean harmful substances contained in exhaust gas,
wherein the high-frequency absorbing layer is made from a
mixture of an electroconductive metal oxide and an
insulating material having an impedance adjusted to the
characteristic impedance of a medium through which a high-frequency
wave is transmitted such that reflection power
ratio becomes 10 dB or more.
According to a second aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
the insulating material is a metal oxide having co-catalytic
activity such as ceria or ceria stabilized zirconia.
According to a third aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
the insulating material is a metal oxide having a large
specific surface area such as g-alumina.
According to a fourth aspect of the present invention,
there is provided a high-frequency heating catalyst which
comprises a catalyst carrying layer, formed on the surface
of a substrate made from a material which rarely absorbs a
high-frequency wave and made from either one or both of a
metal oxide having co-catalytic activity and a metal oxide
material having a large specific surface area, which a
catalyst material such as Pd, Pd/Rh or Pt/Rh for making
clean harmful substances contained in exhaust gas is
uniformly dispersed in and carried by, and a high-frequency
absorbing layer formed on part of the surface of the
catalyst carrying layer and made from a mixture of an
insulating material and an electroconductive metal oxide,
wherein the high-frequency absorbing layer is formed on an
upstream side of exhaust gas to be cleaned.
According to a fifth aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
the insulating material contains either one or both of a
metal oxide having co-catalytic activity and a metal oxide
material having a large specific surface area, which a
catalyst such as Pd, Pd/Rh or Pt/Rh for making clean harmful
substances contained in exhaust gas is uniformly dispersed
in and carried by.
According to a sixth aspect of the present invention,
there is provided a high-frequency heating catalyst which
comprises a wash coat layer formed on the surface of a
substrate made from a material which rarely absorbs a high-frequency
wave and made from a heat resistant material such
as g-alumina or ceria stabilized zirconia having a large
specific surface area, and a high-frequency absorbing layer
formed on part of the surface of the wash coat layer and
made from a mixture of an electroconductive metal oxide and
an insulating material and which has a catalyst such as Pt,
Pt/Rh or Pd/Rh for making clean harmful substances contained
in exhaust gas carried on the surfaces or in the vicinity of
the surfaces of the wash coat layer and the high-frequency
absorbing layer, wherein the high-frequency absorbing layer
is formed on an upstream side of exhaust gas to be cleaned.
According to a seventh aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
the high-frequency absorbing layer contains a co-catalyst
material such as ceria or ceria stabilized zirconia having
co-catalytic activity and g-alumina or ceria stabilized
zirconia having a large specific surface area.
According to an eighth aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
the material having co-catalytic activity and the heat
resistant material do not contain an element which reacts
with a metal element contained in the electroconductive
metal oxide.
According to a ninth aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
an intermediate layer made from a metal oxide which does not
contain a component reacting with a metal element component
contained in the high-frequency absorbing layer at high
temperatures is formed between the high-frequency absorbing
layer and the substrate.
According to a tenth aspect of the present invention,
there is provided a high-frequency heating catalyst, wherein
when an electroconductive metal oxide containing Co is used
as a high-frequency absorbing material, a metal oxide
containing no Al, such as SiO2, ZrO2 or CeO2, or a composite
metal oxide of two or more thereof is used to form the
intermediate layer.
According to an eleventh aspect of the present
invention, there is provided a high-frequency heating
catalyst, wherein when an electroconductive metal oxide
containing Mn is used as a high-frequency absorbing
material, a metal oxide containing no Si, such as CaO,
Al2O3 or CeO2, or a composite metal oxide of two or more
thereof is used to form the intermediate layer.
The above and other objectives, features and
advantages of the invention will become more apparent from
the following description when taken in conjunction with
the accompanying drawings.
Brief Description of the Drawings
Figs. 1(a) to 1(c) are diagrams showing the structure of
cleaning mean comprising a high-frequency heating catalyst
according to Embodiment 1 of the present invention;
Fig. 2 is a diagram showing the constitution of an
exhaust gas cleaning apparatus according to Embodiment 1 of
the present invention;
Fig. 3 is a diagram showing the structure of cleaning
means according to Embodiment 2 of the present invention;
Fig. 4 is a diagram showing the structure of cleaning
means according to Embodiment 3 of the present invention;
Figs. 5(a) to 5(d) are diagram showing the structure of
a high-frequency heating catalyst according to Embodiment 4
of the present invention;
Fig. 6 is a diagram showing the structure of another
high-frequency heating catalyst according to Embodiment 4 of
the present invention;
Fig. 7 is a diagram showing the structure of still
another high-frequency heating catalyst according to
Embodiment 4 of the present invention;
Fig. 8 is a diagram showing the constitution of an
exhaust gas cleaning apparatus of the prior art;
Figs. 9(a) and 9(b) are diagrams showing the
constitution of cleaning means of the prior art; and
Figs. 10(a) and 10(b) are diagrams showing the
constitution of another cleaning means of the prior art.
Detailed Description of the Preferred Embodiments
Preferred Embodiments of the present invention will
be described hereinunder with reference to the
accompanying drawings.
In the following description, the same or
corresponding elements as those of the prior art are given
the same reference symbols.
Embodiment 1
Figs. 1(a), 1(b) and 1(c) are diagrams showing the
structure of exhaust gas cleaning means 23 according to
Embodiment 1 of the present invention. The cleaning means
23 comprises (1) a substrate 1 composed of a cordierite
sintered body having a honeycomb structure, insulating
properties and high thermal shock resistance and (2) a
high-frequency heating catalyst 2 coated on the surface of
each barrier 1K of the substrate 1. In these figures,
reference symbol 1s denotes through holes formed in the
substrate 1. As shown in Fig. 1(c), exhaust gas G is made
clean by the high-frequency heating catalyst 2 while it
passes through the through holes 1s in the cleaning means
23 and discharged.
The high-frequency catalyst 2 has Pt/Rh, a three-element
catalyst, carried by a high-frequency absorbing
layer made from a mixture of La0.6Sr0.4MnO3 which is an
electroconductive metal oxide and ceria stabilized
zirconia which is an insulating material having co-catalytic
activity and a large specific surface area. The
mixing ratio of the electroconductive metal oxide and the
insulating material is controlled to adjust the impedance
of the high-frequency absorbing layer to the
characteristic impedance of a transmission path through
which a high-frequency wave is transmitted such that
reflection power ratio becomes 10 dB or more at an
oscillation frequency of a microwave. The high-frequency
absorbing layer is coated on the substrate 1 and then
heated to be firmly fixed to the barrier 1K of the
substrate 1.
The Pt/Rh three-element catalyst is carried on the
surface or in the interior of the high-frequency absorbing
layer by immersing the substrate 1 having the high-frequency
absorbing layer formed thereon in a solution
containing Pt/Rh and heating it. Since ceria stabilized
zirconia which is an insulating material contained in the
high-frequency absorbing layer has a large specific
surface area, the Pt/Rh catalyst can be uniformly
dispersed into the high-frequency absorbing layer.
Fig. 2 is a diagram showing the constitution of an
exhaust gas cleaning apparatus equipped with the cleaning
means 23 having the above high-frequency heating medium 2.
A microwave generated by a high-frequency oscillator 25
passes through a waveguide path 26 and is transmitted to a
cylindrical heating chamber 22 (cavity) whose impedance is
adjusted to the impedance of the waveguide path 26 in a
joint slot 28. The exhaust gas G is guided from an
exhaust pipe 21 into the heating chamber 22 and discharged
from an exhaust pipe 21b. Reflection plates 27a and 27b
made from a punching metal are installed at both ends of
the heating chamber 22, and the inner diameter and length
of the heating chamber 22 are designed such that a
microwave resonates in the heating chamber 22. In Fig. 2,
reference letter P indicates the field strength of a
standing wave in the heating chamber 22, and the high-frequency
heating medium 2 is held by a supporting member
24 at a position of λg/4 (λg is a wavelength in the
waveguide) from the reflection plate 27b installed on a
downstream side of exhaust gas G in the heating chamber
22, that is, a position where the amplitude of the
standing wave is maximum.
Since the material of the high-frequency heating
catalyst 2 is designed to adjust the impedance of the
high-frequency absorbing layer of the high-frequency
heating catalyst 2 to the characteristic impedance of the
propagation path of the heating chamber 22 as described
above, the reflection of a microwave by the cleaning means
23 is small and the energy of the microwave irradiated
onto the high-frequency heating catalyst 2 is absorbed by
the high-frequency absorbing layer efficiently.
Therefore, the temperature of the catalyst contained in
the high-frequency heating catalyst 2 can be sharply
increased, the temperature of the catalyst can be raised
to its operation temperature quickly even at the time of
the start of an internal combustion engine at low
temperatures, and harmful exhaust gas exhausted at the
time of start at low temperatures can be made clean.
For example, when a microwave having an output power
of 600 W and a frequency of 2.45 GHz generated by the
high-frequency oscillator 25 was irradiated onto the
cleaning means 23, it took about 20 seconds to increase
the surface temperature of the conventional high-frequency
heating catalyst 2B to 400°C. On the other hand, when the
high-frequency heating catalyst 2 of Embodiment 1 was
used, it took about 8 seconds to increase its surface
temperature to 400°C. Since ceria stabilized zirconia
which is an insulating material contained in the high-frequency
heating catalyst 2 has co-catalytic activity,
the catalytic function of the Pt/Rh catalyst is improved,
whereby the cleaning function of harmful exhaust gas of
the catalyst is further enhanced.
According to this Embodiment 1 of the present
invention, the impedance of the high-frequency absorbing
layer in the high-frequency heating catalyst 2 is adjusted
to the characteristic impedance of the propagation path
through which a microwave is transmitted such that
reflection power ratio becomes 10 dB or more at an
oscillation frequency of the microwave. Therefore, the
reflection of the microwave by the high-frequency
absorbing layer is small, the temperature of the catalyst
can be raised sharply, and the temperature of the catalyst
can be increased to its operation temperature quickly even
at the time of the start of an internal combustion engine
at low temperatures, thereby making it possible to make
clean harmful exhaust gas exhausted at the time of start
at low temperatures. Since ceria stabilized zirconia
which is an insulating material contained in the high-frequency
heating catalyst 2 has co-catalytic activity and
a large specific surface area, the catalytic function of
the Pt/Rh catalyst is improved, whereby the cleaning
function of the harmful exhaust gas of the catalyst can be
enhanced.
In this Embodiment 1, ceria stabilized zirconia is
used as the insulating material. When a mixture of a
metal oxide having a high specific surface area such as γ-alumina
having a large specific surface area and ceria
having co-catalytic activity is used, the same effect as
above is obtained.
In the above embodiment, after the high-frequency
absorbing layer is formed on the substrate 1, the Pt/Rh
catalyst is carried on the surface or in the interior of
the high-frequency absorbing layer. When a slurry of a
mixture of the above electroconductive metal oxide and the
insulating material is mixed with a solution containing a
catalyst such as Pt/Rh and stirred to prepare a solution
and the solution is coated on the substrate 1 to form the
high-frequency heating catalyst 2, the catalyst such as
Pt/Rh is uniformly dispersed into the high-frequency
absorbing material. Therefore, the catalytic function of
the high-frequency heating catalyst 2 can be further
improved.
Embodiment 2
Fig. 3 is a diagram showing the structure of exhaust
gas cleaning means 23 according to Embodiment 2 of the
present invention. The cleaning means 23 comprises (1) a
substrate 1 composed of a cordierite sintered body having
a honeycomb structure, insulating properties and high
thermal shock resistance, and (2) a high-frequency heating
catalyst 2 formed on the surface of each barrier 1K of the
substrate 1. The high-frequency heating catalyst 2
comprises a first catalyst carrying layer 3 comprising
ceria stabilized zirconia and a Pd/Rh catalyst, and a
second catalyst carrying layer 4, formed on part of the
surface of the fist catalyst carrying layer 3, which is a
high-frequency absorbing layer comprising La0.6Sr0.4MnO3
and ceria stabilized zirconia having co-catalytic ability
and a Pd catalyst. The second catalyst carrying layer 4
is formed on an upstream side of exhaust gas G to be
cleaned.
The second catalyst carrying layer 4 is formed by
preparing a slurry comprising La0.6Sr0.4MnO3, an
electroconductive metal oxide, and ceria stabilized
zirconia, an insulating material, whose mixing ratio is
controlled to adjust the impedance of the second catalyst
carrying layer 4 to the characteristic impedance of a
transmission path through which a high-frequency wave is
transmitted such that reflection power ratio becomes 10 dB
or more and dip coating the slurry on the first catalyst
carrying layer 3. The second catalyst carrying layer 4
can be formed on only one side of the substrate 1 by
immersing only one side of the substrate 1 into the
slurry.
The cleaning means 23 comprising the above high-frequency
heating catalyst 2 was installed in an exhaust
gas cleaning apparatus as shown in Fig. 2 like the above
Embodiment 1, exhaust gas from an internal combustion
engine while idling was caused to flow through the
apparatus, and the cleaning means 23 was irradiated with a
microwave generated from the high-frequency oscillator 25
and having an output power of 800 W and a frequency of
2.45 GHz. When the cleaning means 23A having the
conventional high-frequency heating catalyst 2B was used,
it took about 20 seconds to increase the surface
temperature of the high-frequency heating catalyst 2B to
its reaction start temperature (about 300°C). On the
other hand, when the cleaning means 23 having the high-frequency
heating catalyst 2 of Embodiment 2 in which the
second catalyst carrying layer 4 was formed in a range of
10 mm on an upstream side of exhaust gas G was used, the
start of a catalytic reaction was observed in about 10
seconds after the irradiation of a microwave.
This is because the reflection of a microwave by the
cleaning means 23 is little and the energy of a microwave
irradiated onto the high-frequency heating catalyst 2 is
efficiently absorbed by the second catalyst carrying layer
4 which is a high-frequency absorbing layer as the
material of the high-frequency heating catalyst 2 is
designed to adjust the impedance of the second catalyst
carrying layer 4 which is a high-frequency absorbing layer
to the characteristic impedance of the propagation path in
the heating chamber 22 such that reflection power ratio
becomes 10 dB or more. Further, since the front (upstream
side of exhaust gas G) of the high-frequency heating
catalyst 2 is heated efficiently by the second catalyst
carrying layer 4, the temperature of the supplied exhaust
gas G rises and catalysts on a downstream side out of the
catalysts contained in the cleaning means 23 are heated by
the supplied exhaust gas G, thereby advancing the start
time of a catalytic reaction.
Moreover, since the second catalyst carrying layer 4
contains ceria stabilized zirconia having co-catalytic
activity and the Pd catalyst, heat is generated by the
catalytic reaction in the front of the high-frequency
heating catalyst 2 at the same time. Therefore, the
temperature of the supplied exhaust gas G rises higher
than when only the high-frequency absorbing layer is
formed at the front of the cleaning means 23, thereby
further quickening a rise in the temperature of the
catalyst.
In the above Embodiment 2, ceria stabilized zirconia
is used as the insulating material for the first catalyst
carrying layer 3. The first catalyst carrying layer 3 may
be formed by containing a catalyst such as Pt/Rh or Pd/Rh
in γ-alumina or a mixture of γ-alumina and ceria. Ceria
stabilized zirconia is used as the insulating material
contained in the second catalyst carrying layer 4. When a
metal oxide such as a mixture of γ-alumina having co-catalytic
activity and a large specific surface and ceria
is used as the insulating material, the same effect is
obtained. It is needless to say that the start time of
the catalytic reaction can be advanced even when a high-frequency
absorbing layer composed of an insulating
material and an electroconductive metal oxide is formed on
an upstream side of exhaust gas in place of the second
catalyst carrying layer 4 because the front of the high-frequency
heating catalyst 2 is heated efficiently, the
temperature of exhaust gas G rises, and catalysts on a
downstream of the cleaning means are heated by the exhaust
gas G.
Embodiment 3
Fig. 4 is a diagram showing the structure of exhaust
gas cleaning means 23 according to Embodiment 3 of the
present invention. The cleaning means 23 comprises (1) a
substrate 1 composed of a cordierite sintered body having
a honeycomb structure, insulating properties and high
thermal shock resistance, and (2) a high-frequency heating
catalyst 2 formed on the surface of each barrier 1K of the
substrate 1. The high-frequency heating catalyst 2
comprises a wash coat layer 5 made from ceria stabilized
zirconia, a high-frequency absorbing layer 6, formed on
part of the surface of the wash coat layer, comprising
La0.6Sr0.4MnO3 and ceria stabilized zirconia, and a
catalyst layer 7 formed from Pd/Rh carried in the vicinity
of the surfaces of the wash coat layer 5 and the high-frequency
absorbing layer 6. The high-frequency absorbing
layer 6 is formed on an upstream side of exhaust gas G to
be cleaned.
The above high-frequency absorbing layer 6 is formed
by preparing a slurry comprising La0.6Sr0.4MnO3, an
electroconductive metal oxide, and ceria stabilized
zirconia, an insulating material, whose mixing ratio is
controlled to adjust the impedance of the high-frequency
absorbing layer 6 to the characteristic impedance of a
transmission path through which a high-frequency wave is
transmitted such that reflection power ratio becomes 10 dB
or more and dip coating the slurry on the wash coat layer
5. The high-frequency absorbing layer 6 can be formed on
only one side of the substrate 1 by immersing only one
side of the substrate 1 into the slurry.
The catalyst layer 7 is carried on the surfaces and
in the interiors of the surfaces of the wash coat layer 5
and the high-frequency absorbing layer 6 by immersing the
substrate 1 having the wash coat layer 5 and the high-frequency
absorbing layer 6 formed thereon in a solution
containing Pd/Rh and heating. Since ceria stabilized
zirconia which is an insulating material contained in the
high-frequency absorbing layer 6 has a large specific
surface area, the Pd/Rh catalyst is carried by the high-frequency
absorbing layer 6 in high concentration.
The cleaning means 23 comprising the above high-frequency
heating catalyst 2 was installed in an exhaust
gas cleaning apparatus as shown in Fig. 2 like the above
Embodiment 1, exhaust gas from an internal combustion
engine while idling was caused to flow through the
apparatus, and the cleaning means 23 having a diameter of
90 mm and a length of 30 mm was irradiated with a
microwave generated from the high-frequency oscillator 25
and having an output power of 800 W and a frequency of
2.45 GHz. When the cleaning means 23B having the
conventional high-frequency heating catalyst 2B was used,
it took about 20 seconds to increase the surface
temperature of the high-frequency heating catalyst 2B to
its catalytic reaction start temperature (about 300°C).
On the other hand, when the cleaning means 23 having the
high-frequency heating catalyst 2 of Embodiment 3 in which
the high-frequency absorbing layer 6 was formed in a range
of 10 mm on an upstream side of exhaust gas G was used,
the start of a catalytic reaction was observed in about 10
seconds after the irradiation of a microwave.
This is because the reflection of a microwave by the
cleaning means 23 is little and the energy of a microwave
irradiated onto the high-frequency heating catalyst 2 is
efficiently absorbed by the high-frequency absorbing layer
6 as the material of the high-frequency heating catalyst 2
is designed to adjust the impedance of the high-frequency
absorbing layer 6 to the characteristic impedance of the
propagation path in the heating chamber 22 such that
reflection power ratio becomes 10 dB or more.
Since the front of the high-frequency heating
catalyst 2 is heated efficiently by the high-frequency
absorbing layer 6, the temperature of the supplied exhaust
gas G rises and the catalyst carried by the wash coat
layer 17 on a downstream side of the cleaning means 23 is
heated by the exhaust gas G, the start time of a catalytic
reaction can be advanced. Further, since the Pd/Rh
catalyst is carried in the vicinity of the surface of the
high-frequency absorbing layer 6 in high concentration, a
large amount of heat is generated by the catalytic
reaction at the same time, thereby making it possible to
further quicken a rise in the temperature of the catalyst.
Further, since the use efficiency of the catalyst is high,
the amount of a precious metal used in the catalyst can be
reduced.
In the above Embodiment 3, ceria stabilized zirconia
is used as the insulating material for the wash coat layer
5. γ-alumina or a mixture of γ-alumina and ceria may be
used.
In the above Embodiments 1, 2 and 3, La0.6Sr0.4MnO3 is
used as the high-frequency absorbing material. When a
composite metal oxide such as La(1-x)SrxCoO3, La(1-x)SrxCrO3,
La(1-x)SrxMnO3, La(1-x)SrxCo(1-y)PdyO3, La(1-x)SrxMn(1-y)PdyO3,
La(1-x)CaxCoO3 or La(1-x)CaxMnO3 (0 < x <
1, 0 < y < 1) or a mixture thereof is used, the same
effect is obtained.
When the above electroconductive metal oxide contains
Mn, if the material forming the layer in contact with the
layer containing the above high-frequency absorbing
material, for example, the first catalyst carrying layer 3
of the above Embodiment 2 or the wash coat layer 5 of the
above Embodiment, is a compound containing Si, Mn and Si
react with each other at high temperatures with the result
that the impedance of the high-frequency absorbing
material forming the second catalyst carrying layer 4 or
the high-frequency absorbing layer 6 changes, thereby
greatly reducing the microwave absorption efficiency of
the high-frequency heating catalyst 2. When the
electroconductive metal oxide contains Co, the layer in
contact with the layer containing the high-frequency
absorbing material must be composed of a compound
containing no Al.
For example, since La0.6Sr0.4MnO3 is used as the high-frequency
absorbing material and ceria stabilized zirconia
is used as the material forming the second catalyst
carrying layer 4 in the above Embodiment 2, even if the
surface temperature of the cleaning means 23 rises, the
above reaction does not occur and a change in the
catalytic activity of the high-frequency heating catalyst
2 is not observed. Since La0.6Sr0.4MnO3 is used as the
high-frequency absorbing material and ceria stabilized
zirconia is used as the material forming the wash coat
layer 5 in the above Embodiment 3, even if the surface
temperature of the cleaning means 23 rises, a change in
the catalytic activity of the high-frequency heating
catalyst 2 is not observed.
Embodiment 4
Figs. 5(a) to 5(d) are diagrams showing the structure of
exhaust gas cleaning means 23 according to Embodiment 4 of
the present invention. Fig. 5(a) is a diagram showing the
outer appearance, Fig. 5(b) is a sectional view, and Fig.
5(c) is a partially enlarged front view of the cleaning means
23. Fig. 5(d) is a diagram typically showing the layer
structure of the high-frequency heating catalyst 2. The
cleaning means 23 comprises (1) a substrate 1 composed of a
cordierite sintered body having a honeycomb structure,
insulating properties and high thermal shock resistance, and
(2) a high-frequency heating catalyst 2 which comprises an
intermediate layer 8A made from ZrO2 and coated on the
surface of each barrier 1K of the substrate 1, a high-frequency
absorbing layer 9A formed on the intermediate layer
and made from a mixture of La0.6Sr0.4CoO3 which is an
electroconductive metal oxide and CeO2 which is an insulating
material, and a catalyst layer 10, formed on the high-frequency
absorbing layer 9A and made from MgO carrying
Pt/Rh.
When the above-structured cleaning means 23 was
installed in the heating chamber 22 of an exhaust gas
cleaning apparatus as shown in Fig. 2 and irradiated with
a microwave generated from the high-frequency oscillator
25 and having an output power of 600 W and a frequency of
2.45 GHz, the surface temperature of the high-frequency
heating catalyst 2 reached about 800°C in 30 seconds due
to the energy of the microwave and heat generated by a
catalytic reaction. At this point, the properties of the
high-frequency absorbing layer 9A of the high-frequency
heating catalyst 2 did not change and the temperature rise
characteristics of the high-frequency heating catalyst 2
hardly changed even when its surface temperature was
raised to about 800°C repeatedly under the above
conditions. Further, the electric resistance of the high-frequency
absorbing layer 9A did not change after the
repeated temperature rise test.
Fig. 6 is a diagram showing the structure of the
high-frequency heating catalyst 2 having a high-frequency
absorbing layer made from an electroconductive metal oxide
containing Mn. The high-frequency heating catalyst 2
comprises an intermediate layer 8B formed on the barrier
1K of the substrate 1 composed of a cordierite sintered
body and made from Al2O3, a high-frequency absorbing layer
9B formed on the intermediate layer 8B and made from a
mixture of La0.6Sr0.4MnO3 which is an electroconductive
metal oxide and CeO2 which is an insulating material, and
a catalyst layer 10, formed on the high-frequency
absorbing layer 9B and made from MgO carrying Pt/Rh. When
the same test as that of the above Embodiment 4 was
carried out using the above-structured high-frequency
heating catalyst 2, the properties of the high-frequency
absorbing layer 9B of the high-frequency heating catalyst
2 did not change and the electric resistance of the high-frequency
absorbing layer 9B did not change after the test
as well.
According to this Embodiment 4, when the material
forming the high-frequency absorbing layer 9A is
La0.6Sr0.4CoO3 containing Co, ZrO2, a metal oxide
containing no Al, is used to form the intermediate layer
8A between the high-frequency absorbing layer 9A and the
substrate 1. When the material forming the high-frequency
absorbing layer 9B is La0.6Sr0.4MnO3 containing Mn, Al2O3,
a metal oxide containing no Si is used to form the
intermediate layer 8B. Therefore, even when the high-frequency
heating catalyst 2 is heated to about 800°C by
microwave radiation, the properties of La0.6Sr0.4CoO3 or
La0.6Sr0.4MnO3 forming the high-frequency absorbing layer
(9A or 9B) do not change and hence, the catalytic function
of the high-frequency heating catalyst 2 does not
deteriorate.
In the above Embodiment 4, the catalyst layer 22A or
22B is formed on the high-frequency absorbing layer 9A or
9B in the above Embodiment 4, and the intermediate layer
8A or 8B is formed between the substrate 1 and the high-frequency
absorbing layer 9A or 9B. As shown in Fig. 7,
also in the high-frequency heating catalyst having a high-frequency
absorbing layer 9C made from a high-frequency
absorbing material carrying a catalyst such as Pt/Rh,
ZrO2,a metal oxide containing no Al, is used to form an
intermediate layer 8C between the barrier 1K of the
substrate 1 and the high-frequency absorbing layer 9C when
the material forming the high-frequency absorbing layer 9C
is La0.6Sr0.4CoO3 containing Co, and Al2O3, a metal oxide
containing no Si, is used to form the intermediate layer
8C when the material forming the high-frequency absorbing
layer 9C is La0.6Sr0.4MnO3 containing Mn.
In the above Embodiment 4, La0.6Sr0.4CoO3 containing
Co or La0.6Sr0.4MnO3 containing Mn is used as the material
forming the high-frequency absorbing layer. La(1-x)SrxCoO3,
La(1-x)SrxCrO3, La(1-x)SrxMnO3, La(1-x)SrxCo(1-y)PdyO3
or La(1-x)SrxMn(1-y)PdyO3 (0 < x < 1, 0 < y < 1) may
be used.
The intermediate layer may be made from a metal oxide
such as MgO, SiO2, CaO or CeO2, or a composite oxide of
two or more thereof in addition to the above ZrO2. MgO,
ZrO2, CaO or CeO2, or a composite metal oxide of two or
more thereof may be used as the metal oxide containing no
Si in addition to the above Al2O3.
As described above, the high-frequency heating
catalyst according to the first aspect of the present
invention comprises a high-frequency absorbing layer
formed on the surface of a substrate made from a material
which rarely absorbs a high-frequency wave and made from a
high-frequency absorbing material and a catalyst such as
Pd, Pd/Rh or Pt/Rh, carried by the high-frequency
absorbing layer, for making clean harmful substances
contained in exhaust gas, and the high-frequency absorbing
layer is made from a mixture of an electroconductive metal
oxide and an insulating material having an impedance
adjusted to the characteristic impedance of a medium
through which a high-frequency wave is transmitted such
that reflection power ratio becomes 10 dB or more.
Therefore, the reflection of high-frequency radiation is
little, the high-frequency wave can be absorbed and
converted into heat energy effectively, and the
temperature of the catalyst can be thereby increased to
its operation temperature quickly at the time of the start
of an internal combustion engine at low temperatures.
Thus, harmful exhaust gas exhausted at the time of the
start at low temperatures can be made clean.
In the high-frequency heating catalyst according to
the second aspect of the present invention, the insulating
material is a metal oxide having co-catalytic activity
such as ceria. Therefore, the catalytic function of the
high-frequency heating catalyst can be further improved.
In the high-frequency heating catalyst according to
the third aspect of the present invention, the insulating
material is a metal oxide having a large specific surface
area such as ceria stabilized zirconia. Therefore, a
catalyst such as Pd, Pd/Rh or Pt/Rh can be uniformly
carried by the high-frequency absorbing layer, and
differences in the function of the high-frequency catalyst
at different sites can be eliminated.
The high-frequency heating catalyst according to the
fourth aspect of the present invention comprises a
catalyst carrying layer, formed on the surface of a
substrate made from a material which rarely absorbs a
high-frequency wave and made from either one or both of a
metal oxide having co-catalytic activity and a metal oxide
material having a large specific surface area, which a
catalyst material such as Pd, Pd/Rh or Pt/Rh for making
clean harmful substances contained in exhaust gas is
uniformly dispersed in and carried by, and a high-frequency
absorbing layer formed on part of the surface of
the catalyst carrying layer and made from a mixture of an
insulating material and an electroconductive metal oxide,
and the high-frequency absorbing layer is formed on an
upstream side of exhaust gas to be cleaned. Therefore,
since exhaust gas heated at an upstream heats a downstream
portion of the high-frequency heating catalyst, the
temperature of the catalyst can be increased to its
operation temperature quickly.
In the high-temperature heating catalyst according to
the fifth aspect of the present invention, the insulating
material contains either one or both of a metal oxide
having co-catalytic activity and a metal oxide material
having a large specific surface area, which a catalyst
such as Pd, Pd/Rh or Pt/Rh for making clean harmful
substances contained in exhaust gas is uniformly dispersed
in and carried by. Therefore, the exhaust gas is further
heated by a catalyst reaction in the high-frequency
absorbing layer at an upstream, thereby making it possible
to increase the temperature of the catalyst to its
operation temperature more quickly.
The high-frequency heating catalyst according to the
sixth aspect of the present invention comprises a wash
coat layer formed on the surface of a substrate made from
a material which rarely absorbs a high-frequency wave and
made from a heat resistant material such as γ-alumina or
ceria stabilized zirconia having a large specific surface
area, and a high-frequency absorbing layer formed on part
of the surface of the wash coat layer and made from a
mixture of an electroconductive metal oxide and an
insulating material, a catalyst such as Pt, Pt/Rh or Pd/Rh
for making clean harmful substances contained in exhaust
gas is carried on the surfaces or in the vicinity of the
surfaces of the wash coat layer and the high-frequency
absorbing layer, and the high-frequency absorbing layer is
formed on an upstream side of exhaust gas to be cleaned.
Therefore, the exhaust gas at an upstream is also heated
by heat generated by a catalytic reaction, thereby making
it possible to increase the temperature of the catalyst to
its operation temperature more quickly.
In the high-frequency heating catalyst according to
the seventh aspect of the present invention, the high-frequency
absorbing layer contains a co-catalyst material
such as ceria or ceria stabilized zirconia having co-catalytic
activity and γ-alumina or ceria stabilized
zirconia having a large specific surface area. Therefore,
the catalytic function of the high-frequency heating
catalyst can be further improved.
In the high-frequency heating catalyst according to
the eighth aspect of the present invention, the material
having co-catalytic activity and the heat resistant
material do not contain an element which reacts with a
metal element contained in the electroconductive metal
oxide. Therefore, the high-frequency catalyst can be used
at a wide temperature range.
In the high-frequency heating catalyst according to
the ninth aspect of the present invention, an intermediate
layer made from a metal oxide which does not contain a
component reacting with a metal element component
contained in the high-frequency absorbing layer at high
temperatures is formed between the high-frequency
absorbing layer and the substrate. Therefore, even when
the high-frequency absorbing material is heated to a high
temperature by the absorption of a microwave, a reaction
does not occur between the material forming the high-frequency
absorbing layer and the material forming the
substrate and the catalyst function does not deteriorate.
Further, since there are no changes in the characteristics
of the high-frequency heating catalyst after long-term
use, the reliability of the high-frequency heating
catalyst can be greatly improved.
In the high-frequency heating catalyst according to
the tenth aspect of the present invention, when the high-frequency
absorbing layer is made from a material
containing Co, a metal oxide containing no Al is used to
form the intermediate layer. Therefore, the composition
of the intermediate layer can be limited in advance.
In the high-frequency heating catalyst according to
the eleventh aspect of the present invention, when the
high-frequency absorbing layer is made from a material
Containing Mn, a metal oxide containing no Si is used to
form the intermediate layer. Therefore, the composition
of the intermediate layer can be limited in advance.
The features disclosed in the foregoing description, in the
claims and/or in the accompanying drawings may, both separately
and in any combination thereof, be material for realising the
invention in diverse forms thereof.