TECHNICAL FIELD
[0001] The present invention relates to: an additive for engine oil to be added to engine
oil as a catalyst component used for assisting combustion of, in particular, particulate
matter (hereinafter, referred to also as PM) so as to purify exhaust gases discharged
from an internal combustion engine such as a diesel engine; the engine oil to which
the additive has been added; and an exhaust gas purifying method that is conducted
so as to purify (convert) toxic components in the exhaust gases.
BACKGROUND ART
[0002] Recently, PM, such as soot, contained in exhaust gases that are discharged from internal
combustion engines, such as diesel engines, have raised serious problems as influences
harmful to the environment and the human body.
For this reason, various applications in which honeycomb structured bodies, which
are made from porous ceramics using silicon carbide, cordierite or the like as materials,
are used as filters for capturing PM in exhaust gases to purify the exhaust gases
have been proposed.
[0003] Among exhaust gas purifying filters, those in which an exhaust gas purifying catalyst,
such as an oxide catalyst and a noble metal catalyst, is supported have been proposed.
In the filter having such an exhaust gas purifying catalyst supported thereon, toxic
gas components such as CO, NO and HC in the exhaust gases can be converted (oxidized)
by the action of such a catalyst, and the burning temperature of the PM is lowered
so that the PM can be burned more efficiently.
[0004] Figs. 6 (a) to (d) are schematic diagrams that schematically show various states
which occur at a partition wall portion of a honeycomb structuredbodywhen the exhaust
gas purifying filter made of the honeycomb structured body is arranged in a pipe connected
to the engine in the prior art structure.
Fig. 6 (a) is a schematic diagram that shows a state in which an exhaust gas purifying
catalyst is supported on an exhaust gas purifying filter made of a honeycomb structured
body, and Fig. 6(b) is a schematic diagram that shows a state in which the filter
is covered with PM and the like.
[0005] In the exhaust gas purifying filter of the above-mentioned type, an exhaust gas purifying
catalyst 61 is supported on each of the partition wall portion 60 of the exhaust gas
purifying filter made of an unused honeycomb structured body so as to contribute to
purification (conversion) of the exhaust gases (see Fig. 6(a)). Here, the exhaust
gas purifying catalyst 61 is also supported on the inside of each wall; however, in
this figure, the catalyst inside the wall is omitted.
When exhaust gases are introduced into the honeycomb structured body, the PM in the
exhaust gases is captured, and accumulated on the surface and the like of the exhaust
gas purifying filter (see Fig. 6(b)).
[0006] It is necessary for the collected PM 62 to be regularly burned and eliminated (the
filter to be regenerated), and for such a process, for example, a post injection system
is mainly used.
At this time, the catalyst supported as described above is made in contact with the
PM so that the burning temperature of the PM is lowered and the PM is efficiently
burned.
DISCLOSURE OF THE INVENTION
PROBLEMS TO BE SOLVED BY THE INVENTION
[0008] Here, in the engine, engine oil is used for the purposes such as protecting, cooling
and sealing sliding portions, and the engine oil contains a large amount of additives
such as calcium salt serving as a cleaning agent. A portion of the additive is introduced
into the combustion chamber through the piston side wall of the engine, and after
having been burned, is captured by the exhaust gas purifying filter together with
PM in the exhaust gases.
[0009] When the PM is burned and eliminated, with the above-mentioned additive being captured
onto each of the partition wall portion 60 of the exhaust gas purifying filter, one
portion of the additive components, made from calcium or the like, remains on the
partition wall portion 60 of the exhaust gas purifying filter as ashes 63 without
beingburned. Moreover, after the regenerating processes have been repeatedly conducted
on the partition wall portion 60 of the exhaust gas purifying filter, the ashes 63
are gradually accumulated to eventually cover the entire exhaust gas purifying catalyst
61 supported on the partition wall portion 60 of the exhaust gas purifying filter
(see Fig. 6(c)).
[0010] Here, in addition to those derived from the additive as described above, ashes include,
for example, those caused by abrasion of the sliding portions of the engine and those
derived from sulfates and the like generated during the burning process.
[0011] In the case where the engine is further driven in this state to cause a fixed amount
of PM 62 accumulated on the ashes 63 as shown in Fig. 6(d), although a regenerating
process that burns the PM 62 needs to be carried out, the PM 62 is not allowed to
contact to the exhaust gas purifying catalyst 61, with the result that the PM 62 is
burned insufficiently.
[0012] When the entire exhaust gas purifying catalyst 61 is thus covered with the ashes
63, the exhaust gas purifying catalyst 61 is not made in contact with the PM accumulated
on the filter to cause the problem that its effects as the PM burning catalyst are
lowered.
[0013] In order to solve this problem, the invention disclosed in Patent Document 1 has
proposed a method in which the flow-in and flow-out directions of the exhaust gases
to and from the exhaust gas purifying filter are switched so that the accumulated
ashes can be discharged from the filter together with exhaust gases.
[0014] In the above-mentioned invention, however, the structure of pipes used for introducing
exhaust gases into the exhaust gas purifying filter becomes complicated to cause the
capacity of a casing in which the filter is installed to become larger; therefore,
when the limited installation space in which the casing has to be placed is taken
into consideration, this structure is not suitable. Moreover, a controlling mechanism
used for switching directions is further required to cause a problem of high costs.
Furthermore, the ashes accumulated on the walls are highly viscous, and are hardly
discharged by a pressure derived from the exhaust gases.
[0015] Moreover, in Patent Document 2, disclosed is an invention proposing use of an engine
oil with a powder of cerium oxide added thereto so that cerium oxide is used as an
exhaust gas purifying catalyst in a combustion chamber of an engine.
[0016] However, when the engine oil with cerium oxide particles added thereto is used, there
was a problem that sufficient catalytic action was not exerted after being accumulated
on the filter.
It can be considered that this is because the specific surface area of the cerium
oxide particle has become small by sintering and the like, and the lattice defect
of oxygen has decreased.
MEANS FOR SOLVING THE PROBLEMS
[0017] As a result of earnest study in view of the above-mentioned problems, the inventors
of the present invention found out that, when an engine oil with an additive for engine
oil added thereto is used, the additive for engine oil comprising a compound containing
a metallic element, wherein a metal oxide obtained by oxidizing the metallic element
is a compound having a catalytic action which promotes burning of PM contained in
exhaust gases discharged from an internal combustion engine, the metal oxide is introduced
into an exhaust gas purifying filter with the exhaust gases after the fuel is burned,
so that it exists as a catalyst which promotes burning of PM particularly on the filter
to promote burning of PM using the catalytic act ion of the existing metal oxide,
and completed an additive for engine oil of the present invention.
In addition, the present inventors completed an invention concerning an engine oil
which contains the above-mentioned additive, and an invention concerning an exhaust
gas purifying method in which exhaust gases are purified even after ashes have been
accumulated, by making the metallic oxide exist in and/or on the ashes accumulated
on the exhaust gas purifying filter so that the metal oxide comes into contact with
the PM.
[0018] Namely, an additive for engine oil of the first aspect of the present invention comprises:
a compound containing a metallic element, wherein a metal oxide obtained by oxidizing
the metallic element has a catalytic action which promotes burning of a particulate
matter contained in exhaust gases discharged from an internal combustion engine.
[0019] Further, the additive for engine oil of the present invention is desirably used for
providing the metal oxide in a filter of an exhaust gas purifying device connected
to a combustion chamber of the internal combustion engine.
[0020] An additive for engine oil of the second aspect of the present invention comprises:
a compound containing a metallic element, wherein the compound containing a metallic
element comprises a metal complex including at least one kind of metallic element
selected from the group consisting of 4th period elements, lanthanoids, and 4th group
elements in the periodic table.
[0021] Further, the additive for engine oil of the first or second aspect of the present
invention is desirably a metal complex represented by a general formula (1) :
M(OR
1)
p(R
2COCHCOR
3)
q (1)
(wherein M is one kind selected from the group consisting of Ce, V, Cr, Mn, Ni, Co,
Cu, Fe, Pb, and Sn;
each of p and q represents a whole number determined such that the metal complex has
a coordination number of 2 to 8, or p or q may be 0;
each of R
1, each of R
2, or each of R
3 may be the same, or may differ when the number of R
1, R
2, or R
3 is 2 or more; and
R
1 and R
2 independently represent an alkyl group with a carbon number of 1 to 6, and R
3 represents an alkyl group with a carbon number of 1 to 6 and/or an alkoxy group with
a carbon number of 1 to 16).
[0022] In the additive for engine oil of the first or second aspect of the present invention,
desirably, R
1 and R
2 in the general formula (1) independently represent: at least one kind selected from
the group consisting of a methyl group, an ethyl group, an n-propyl group, an iso-propyl
group, an n-butyl group, a tert-butyl group, an n-pentyl group, and a 2-ethoxyethyl
group, and R
3 represents: at least one kind selected from the group consisting of a methyl group,
an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, a tert-butyl
group, an n-pentyl group, and a 2-ethoxyethyl group; and/or at least one kind selected
from the group consisting of a methoxy group, an ethoxy group, an n-propoxy group,
an iso-propoxy group, an n-butoxy group, a tert-butoxy group, a 2-ethylhexyloxy group,
and a lauryloxy group.
[0023] The additive for engine oil of the first or second aspect of the present invention
is desirably a metal complex represented by the following formula (2) :

(wherein R
4 to R
9 independently represent a hydrogen or the alkyl group, M is one kind selected from
the group consisting of Ce, V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn, and m is 1 or 2)
[0024] The additive for engine oil of the first or second aspect of the present invention
is desirably a metal complex represented by the following formula (3):

(wherein R
10 to R
15 independently represent hydrogen or the alkyl group, M is one kind selected from
the group consisting of Ce, V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn, and n is 1 or 2)
[0025] The additive for engine oil of the first or second aspect of the present invention
is desirably a metal complex represented by the following formula (4):

(wherein R
16 to R
25 independently represent a hydrogen or the alkyl group, wherein R
26 is a hydrogen or does not exist, and M is one kind selected from the group consisting
of Ce, V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn)
[0026] In the additive for engine oil of the first or second aspect of the present invention,
desirably, the metallic element is cerium.
[0027] In the additive for engine oil of the first or second aspect of the present invention,
desirably, the compound containing a metallic element is a metal complex which has
a trivalent or tetravalent cerium ion as a central metal.
[0028] An engine oil of the third aspect of the present invention comprises the additive
for engine oil composed of any of the above-mentioned compounds containing a metallic
element.
[0029] In the engine oil of the present invention, desirably, the added amount of the additive
for engine oil is 1 to 10% by weight.
[0030] An exhaust gas purifying method of the fourth aspect of the present invention comprises:
an exhaust gas purifying method using an additive for engine oil comprising a compound
containing a metallic element, wherein an engine oil including the additive for engine
oil is used, a metal oxide obtained by oxidizing the metallic element has a catalytic
action which promotes burning of a particulate matter contained in exhaust gases discharged
from an internal combustion engine, and the metal oxide is provided in the filter
of an exhaust gas purifying device connected with a combustion chamber of the internal
combustion engine by introducing the compound containing a metallic element into the
combustion chamber of the internal combustion engine to purify exhaust gases using
the catalytic action of the metal oxide provided in the filter of the exhaust gas
purifying device.
[0031] In the exhaust gas purifying method, desirably, the filter of the exhaust gas purifying
device is a honeycomb structured body comprising: a plurality of cells in the longitudinal
direction with a cell wall therebetween; and a plug that seals either one of the ends
of the cell so that exhaust gases flow through the cell wall.
EFFECTS OF THE INVENTION
[0032] The additive for engine oil of the first aspect of the present invention comprising
a compound containing a metallic element can be dissolved in engine oil, thereby,
after being introduced into a combustion chamber of the engine, and when an ash is
accumulated on the exhaust gas purifying filter, exists as a metal oxide in the ash
and/or on the ash, so that it can function as a catalyst for promoting burning of
PM.
Even after the engine is driven for a long period of time and PM is accumulated, a
catalyst deriving from the engine oil can come into contact with the PM to assist
burning of PM (regeneration of the filter) . As a result, regenerating rate of the
filter can be improved.
[0033] The regeneration rate of the exhaust gas purifying filter refers to how close the
weight of the exhaust gas purifying filter which increased from accumulated PM becomes
by regenerating process to the weight immediately after the last regeneration, and
the more the weight of the exhaust gas purifying filter subjected to the regenerating
process is close to the weight of the exhaust gas purifying filter immediately after
the last regeneration, the higher the regeneration rate is.
[0034] The additive for engine oil of the second aspect of the present invention comprising
a compound containing a metallic element can be dissolved in engine oil, since it
serves as a metal complex, thereby, after being introduced into a combustion chamber
of the engine, and when an ash is accumulated on the exhaust gas purifying filter,
exists as a metal oxide in the ash and/or on the ash, so that it can function as a
catalyst for promoting burning of PM.
Even after the engine is driven for a long period of time and PM is accumulated, a
catalyst deriving from the engine oil can come into contact with the PM to assist
burning of PM (regeneration of the filter). As a result, regenerating rate of the
filter can be improved.
[0035] The engine oil of the third aspect of the present invention includes the additive
for engine oil of the first or second aspect of the present invention comprising a
compound containing a metallic element; therefore, when this engine oil is used, after
the engine oil is introduced into a combustion chamber of the engine, and when an
ash is accumulated on the exhaust gas purifying filter, a metal oxide can exist in
the ash and/or on the ash, so that it can function as a catalyst for promoting burning
of PM.
Even after the engine is driven for a long period of time and PM is accumulated, a
catalyst deriving from the engine oil can come into contact with the PM to assist
burning of PM (regeneration of the filter). As a result, regenerating rate of the
filter can be improved.
[0036] In the exhaust gas purifying method of the fourth aspect of the present invention,
a compound containing a metallic element is added to an engine oil; therefore, after
the engine oil is introduced into a combustion chamber of the engine, and when an
ash is accumulated on the exhaust gas purifying filter, a metal oxide can exist in
the ash and/or on the ash, so that it can function as a catalyst for promoting burning
of PM.
Even after the engine is driven for a long period of time and PM is accumulated, a
catalyst deriving from the engine oil can come into contact with the PM to assist
burning of PM (regeneration of the filter) . As a result, regenerating rate of the
filter can be improved.
According to this method, without installing a special exhaust gas purifying device
or using a special operating method, purification of exhaust gases can be carried
out efficiently over a long period of time with the same exhaust gas purifying filter.
BEST MODE FOR CARRYING OUT THE INVENTION
[0037] First, an additive for engine oil of the first aspect and the second aspect of the
present invention, as well as an engine oil of the third aspect of present invention,
to which the above-mentioned additive for engine oil is added, will be described.
Hereinafter, in the present specification, as long as there is no particular notice,
the first aspect of the present invention and the second aspect of the present invention
are described without distinction.
[0038] The additive for engine oil of the first aspect of the present invention comprises:
a compound containing a metallic element, wherein a metal oxide obtained by oxidizing
the metallic element has a catalytic action which promotes burning of a particulate
matter contained in exhaust gases discharged from an internal combustion engine.
[0039] The additive for engine oil of the second aspect of the present invention comprises:
a compound containing a metallic element, wherein the compound containing a metallic
element comprises a metal complex including at least one kind of metallic element
selected from the group consisting of 4th period elements, lanthanoids, and 4th group
elements in the periodic table.
[0040] The additive for engine oil of the present invention is used by being added to an
engine oil; the engine oil is that in which an additive such as a cleaning agent,
a abrasion-proof agent, a dispersing agent, a viscosity index improving agent, a pour
point depressant (superplasticizer), and an antioxidant is added to a mineral oil,
a chemical synthetic oil, or a partial synthetic oil serving as a base oil at the
rate of 15 to 30% by weight in total of the whole mixture, and those having various
combinations are commercially available.
[0041] Among the additives, as a cleaning agent, a metallic cleaning agent is mostly used,
examples thereof including: neutral salt which is an alkaline earth metal salt of
organic acids, such as fatty acids having carbon numbers of 8 to 22, or an overbased
compound containing a carbonate of alkaline earth metal salt (particularly calcium
salt, magnesium salt), and normally about 0.5 to 10% by weight thereof is added to
the engine oil.
Metallic components such as the above-mentioned calcium and magnesium turn into a
component of the ash which is accumulated on the exhaust gas purifying filter.
[0042] Although the additive for engine oil is an additive used as one kind of additive
added to the engine oil, as of the above-mentioned additives, in order to use the
additive as an additive for engine oil, the additive is desirably capable of dissolving
in the base oil, or dispersing in the base oil in a colloid-like form.
In a case where the additive for engine oil cannot be dissolved or dispersed in the
base oil, the additive component precipitates at the bottom of a container which stores
the engine oil, thereby it becomes difficult to inject the additive component into
the engine. Even if injection is possible, the flowability of the engine oil is obstructed
within the engine, resulting in the worst case that destruction of the engine may
occur.
[0043] As the additive for engine oil, desirably, a compound containing a metallic element
whose oxide functions as a catalyst which promotes burning of PM is used.
Moreover, the additive for engine oil is desirably capable of being used for providing
the metal oxide in the filter of the exhaust gas purifying device connected to the
combustion chamber of the internal combustion engine.
[0044] Although the type of the metallic element is not particularly limited, a metallic
element selected from the group consisting of 4th period elements, lanthanoids, and
4th group elements in the periodic table is desirably used, and particularly, one
kind of metallic element selected from the group consisting of Ce, V, Cr, Mn, Ni,
Co, Cu, Fe, Pb, and Sn is desirably used as the metallic element.
The additive for engine oil may contain in the compound two or more kinds of different
metallic elements among the above-mentioned metallic elements. It may also be an additive
which is a mixture of two or more kinds of compounds, each of which contain different
metallic elements among the above-mentioned metallic elements.
Moreover, when two or more kinds of different metallic elements are contained in the
additive for engine oil, the two or more kinds of different metallic elements may
be two or more kinds of metallic elements whose multiple oxide functions as a catalyst
which promotes burning of PM.
[0045] Although the type of the compound containing a metallic element is not particularly
limited, from the viewpoint of availability and stability, a complex having an alcohol
represented by R
1OH (wherein R
1 represents an alkyl group having a carbon number of 1 to 6) and a diketone represented
by R
2COCH
2COR
3 (wherein R
2 represents an alkyl group having a carbon number of 1 to 6, and R
3 represents an alkyl group having a carbon number of 1 to 6, or an alkoxy group having
a carbon number of 1 to 16) as ligands is suitably used. A more desirable complex
is a metal complex having a diketone as a ligand. With the complex having diketones
as ligands, ametal complex soluble to the engine oil can be prepared.
[0046] In the present invention, an organometallic complex, a complex compound containing
a metallic element, a coordination compound containing a metallic element, a metallic
complex salt (salt containing a metallic element and a complex ion), a metal cluster,
a cluster complex, a metal cluster complex, and a compound containing any of these
complexes, are generically referred to as a metal complex.
[0047] Further, the additive for engine oil is desirably a metal complex represented by
a general formula (1):
M(OR
1)
p(R
2COCHCOR
3)
q (1)
(wherein M is one kind selected from the group consisting of Ce, V, Cr, Mn, Ni, Co,
Cu, Fe, Pb, and Sn;
each of p and q represents a whole number determined such that the metal complex has
a coordination number of 2 to 8 or p or q may be 0;
each of R
1, each of R
2, or each of R
3 may be the same, or may differ when the number of R
1, R
2, or R
3 is 2 or more; and
R
1 and R
2 independently represent an alkyl group with a carbon number of 1 to 6, and R
3 represents an alkyl group with a carbon number of 1 to 6 and/or an alkoxy group with
a carbon number of 1 to 16) .
[0048] In the additive for engine oil, desirably, R
1 and R
2 in the general formula (1) independently represent: at least one kind selected from
the group consisting of a methyl group, an ethyl group, an n-propyl group, an iso-propyl
group, an n-butyl group, a tert-butyl group, an n-pentyl group, and a 2-ethoxyethyl
group, and R
3 represents: at least one kind selected from the group consisting of a methyl group,
an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, a tert-butyl
group, an n-pentyl group, and a 2-ethoxyethyl group; and/or at least one kind selected
from the group consisting of a methoxy group, an ethoxy group, an n-propoxy group,
an iso-propoxy group, an n-butoxy group, a tert-butoxy group, a 2-ethylhexyloxy group,
and a lauryloxy group.
For example, when the general formula represents Ce(OR
1)
3(R
2COCHCOR
3)
1, the three (OR
1) may differ from each other, such as (OCH
3) (OC
2H
5) (O-iso-C
3H
7).
[0049] Although a specific example of these metal complexes is not what is limited to below,
examples thereof include: Ce(O-iso-C
3H
7)
3, Ce(O-iso-C
3H
7)
4, Ce(O-tert-C
4H
9)
4, Ce(OCH
2CH
2OCH
3)
4, Ce(CH
3-CO-CH=CO-CH
3)
3, Ce(CH
3-CO-CH=CO-CH
3)
4, Ce(O-iso-C
3H
7)
2(CH
3-CO-CH=COCH
3)
2, Ce(O-iso-C
3H
7)
2(C
2H
5OCO-CH=COCH
3)
2, Ce(CH
3OCO-CH=COCH
3)
4, Ce(tert-C
4H
9-CO-CH=CO-tert-C
4H
9)
4, Cu(CH
3-CO-CH=CO-CH
3)
2, Pb(CH
3-CO-CH=CO-CH
3)
2, Ni(CH
3-CO-CH=CO-CH
3)
2, V(CH
3-CO-CH=CO-CH
3)
3, Cr(CH
3-CO-CH=CO-CH
3)
3, Mn(CH
3-CO-CH=CO-CH
3)
3, Fe(CH
3-CO-CH=CO-CH
3)
3, CO(CH
3-CO-CH=CO-CH
3)
3, and Sn(CH
3-CO-CH=CO-CH
3)
2.
[0050] As a compound containing a metallic element, 1, 8-naphthalenediolates represented
by the following formula (2) :

(wherein R
4 to R
9 independently represent a hydrogen or an alkyl group, M is one kind selected from
the group consisting of Ce, V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn, and m is 1 or 2)
is also suitably used.
By using such complex salt with a ligand having a naphthalene nucleus, a metal complex
soluble to the engine oil can be obtained.
[0051] As a compound containing a metallic element, 1, 8-naphthalene-dicarboxylic-acid salts
represented by the following formula (3):

(wherein R
10 to R
15 independently represent a hydrogen or an alkyl group, M is one kind selected from
the group consisting of Ce, V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn, and n is 1 or 2)
is also suitably used.
By using such complex salt with a ligand having a naphthalene nucleus, a metal complex
soluble to the engine oil can be obtained.
[0052] As a compound containing a metallic element, a bis-cyclopentadienyl complex salt
represented by the following formula (4):

(wherein R
16 to R
25 independently represent a hydrogen or an alkyl group, R
26 is a hydrogen or does not exist, and M is selected from the group consisting of Ce,
V, Cr, Mn, Ni, Co, Cu, Fe, Pb, and Sn) is also suitably used.
By using such complex salts, the metal complex can serve as a compound containing
a metallic element which is soluble to the engine oil.
[0053] Among the above-mentioned metallic elements, particularly, a compound containing
cerium is desirably used as the additive for engine oil of the present invention.
The reason is because the compound containing cerium is widely used as a catalyst
which promotes burning of PM, and functions as a catalyst which promotes burning of
PM when accumulated and existing on the exhaust gas purifying filter.
[0054] Here, the exhaust gas purifying function of the cerium compound will be described.
It is known that the cerium compound functions as an exhaust gas purifying catalyst
particularly because of its oxygen storage ability. Specifically, the cerium compound
has a function to release oxygen by the reaction of 2CeO
2 → Ce
2O
3+1/2O
2, and a function to occlude the oxygen by a reverse reaction thereof.
At the time of burning the PM, oxygen required for the burning is provided so that
burning of the PM is promoted; thus the burning temperature of PM can be lowered,
leading to decrease in energy required for filter regeneration.
[0055] Therefore, the cerium compound is desirably composed as an additive having a form
which can be dissolved or dispersed in the base oil.
In particular, a metal complex having a trivalent or tetravalent cerium ion as the
central metal is desirably added thereto, and as the metal complex having the trivalent
cerium ion, the metal complexes represented by the general formula (1) or 4 are proposed.
As the metal complex having the tetravalent cerium ion, the metal complexes represented
by the general formula (1), (2) or (3) are proposed.
[0056] In the present invention, these compounds containing a metallic element may be used
by one kind, or may be used in a desired combination of two or more kinds. Moreover,
a partial hydrolysate of these compounds can also be used.
[0057] The additive for engine oil of the first and second aspect of the present invention
comprising a compound containing a metallic element can be dissolved in the engine
oil since the complex salt soluble to the organic solvent having a hydrophobic ligand
is used. Thus, when the engine oil of the third aspect of present invention with the
same additive added thereto is used, the additive component can be easily introduced
into the inner part of the engine.
[0058] The added amount of the additive for engine oil to the engine oil is desirably 1
to 10% by weight. With the added amount of less than 1%, the amount at which the additive
as a catalyst comes into contact with the PM becomes small, which tends to decrease
the effect which promotes burning of PM, and when the added amount is more than 10%,
the flowability of oil tends to become poor.
[0059] The metallic element contained in the additive in the engine oil enters the combustion
chamber of an engine, and together with burning of a fuel, is oxidized thereafter
to become a metal oxide so that it is introduced into the exhaust gas purifying filter
with the PM in exhaust gases. Note that the exhaust gas purifying method using the
additive for engine oil will be described later in detail.
[0060] On the basis of the above-mentioned description, it can be said that the metal oxide
functions as a catalyst for promoting burning of the PM. Through the filter regenerating
process, if the metal oxide exists on a filter as an ash, the metal oxide functions
as an exhaust gas purifying catalyst on the filter and as a catalyst for promoting
burning of PM.
Even after the engine is driven for a long period of time and PM is accumulated, the
catalyst deriving from the engine oil can come into contact with the PM to assist
the burning of PM (regeneration of the filter) . As a result, the regeneration rate
of the filter can be improved.
[0061] Next, the exhaust gas purifying method of the fourth aspect of the present invention
will be described.
The exhaust gas purifying method of the fourth aspect of the present invention comprises:
an exhaust gas purifying method using an additive for engine oil comprising a compound
containing a metallic element, wherein an engine oil including the additive for engine
oil is used, a metal oxide obtained by oxidizing the metallic element has a catalytic
action which promotes burning of a particulate matter contained in exhaust gases discharged
from an internal combustion engine, and the metal oxide is provided in the filter
of an exhaust gas purifying device connected with a combustion chamber of the internal
combustion engine by introducing the compound containing a metallic element into the
combustion chamber of the internal combustion engine to purify exhaust gases using
the catalytic action of the metal oxide provided in the filter of the exhaust gas
purifying device.
[0062] That is, in the fourth aspect of the present invention, first, using the engine oil
with the compound containing a metallic element added thereto, the compound containing
a metallic element is introduced into the combustion chamber of the internal combustion
engine so that, together with the PM generated by burning the fuel, the metal oxide
is accumulated on the inside of the filter of the exhaust gas purifying device connected
to the combustion chamber of the internal combustion engine.
Hereinafter, description will be given of a case using a diesel engine as the internal
combustion engine, and an engine oil added thereto a cerium compound as the compound
containing a metallic element.
[0063]
Fig. 1 is a view that schematically shows one part of a diesel engine, and an exhaust
gas purifying device connected to the diesel engine.
Figs. 2(a) to (d) are schematic diagrams that schematically show various states which
occur at a partition wall portion of a honeycomb structured body when the exhaust
gas purifying filter comprising the honeycomb structured body is arranged in a pipe
connected with the engine in the fourth aspect of the present invention.
Although in the fourth aspect of the present invention the filter of the exhaust gas
purifying device is not particularly limited, in Fig. 1, an aggregated honeycomb structured
body 40 is provided as a filter.
Description of the aggregated honeycomb structured body will be given later in detail.
[0064] When a diesel engine 81 is driven, first an intake valve 82 opens, and while piston
89 descends from an upper dead point, an intake port 83 draws air into a combustion
chamber 93.
Then, intake valve 82 closes, and while piston 89 ascends from a bottom dead point,
the air drawn into the combustion chamber 93 is compressed so that it becomes high
temperature.
[0065] To the air which was compressed in this way and became a high temperature of 600°C
or more, a fuel whose pressure is enhanced to 100 atm or more is injected from a fuel
injection pump 86, to make the fuel burn by self-ignition so that the piston 89 descends.
When the piston 89 falls to the bottom dead point through burning, an exhaust valve
84 opens, and while the piston 89 ascends from the bottom dead point, exhaust gas
(combustion gas) is discharged from an exhaust port 85.
Considering the above-mentioned process as one cycle, a crank shaft 91 rotates two
times in one cycle, and thereby, force is obtained.
[0066] Here, an engine oil 92 has a roll to prevent wearing out and overheating of the piston
89 and an outer wall portion 87 of the engine, both of which are made of metal, due
to the piston 89 and the outer wall portion 87 made into contact with one another,
together with a roll to prevent leakage of compressed gas and explosion gas by filling
the gap between the piston 89 and the outer wall portion 87. However, some of the
engine oil 92 leak out into the combustion chamber 93 from the gap between the piston
89 and the outer wall portion 87, and is burned with the fuel.
During this process, the additives added in the engine oil 92 are also applied to
burning and an inflammable additive is burned off; however, a non flammable additive
such as a metallic cleaning agent is discharged from the exhaust port 85 without being
burned.
[0067] With respect to the cerium compound added to the engine oil 92, while the chemical
structure thereof changes with burning, as a cerium metal it is not burned off, but
is discharged from the exhaust port 85 with the exhaust gas, mainly in the form of
a cerium oxide.
[0068] The exhaust port 85 and the like of the diesel engine 81 is connected to an introducing
pipe 24 of an exhaust gas purifying device 200, the aggregated honeycomb structured
body 40 is placed in a metal casing 23 of the exhaust gas purifying device 200, so
that it serves as a flowpath of the exhaust gas, and an exhaust pipe 25 is connected
to the outside of the other end of the exhaust purifying device 200. In Fig. 1, the
arrows show the flow of the exhaust gas.
[0069] Therefore, the exhaust gas generated in the diesel engine 81 is introduced into the
inner part of the filter (the aggregated honeycomb structured body 40) through the
exhaust port 85 and the introducing pipe 24, so that the PM in the exhaust gas is
captured by the aggregated honeycomb structured body 40.
Here, the cerium oxide and the noncombustible additive such as the metallic cleaning
agent which have been discharged with the exhaust gas from the exhaust port 85, are
also captured by the aggregated honeycomb structured body 40, together with the PM.
[0070] If a predetermined amount of PM is accumulated thereafter, the pressure loss will
become large to affect the engine; thus, a regenerating process of the filter accompanied
by burning of the PM, is carried out. Even after this regenerating process, the cerium
oxide remains in the ash inside the aggregated honeycomb structured body 40 to thereafter
be made in contact with the accumulated PM, thereby functioning as a catalyst for
promoting burning of the PM. The catalytic action of the accumulated cerium oxide
can thus promote burning of the PM.
[0071] Normally, an exhaust gas purifying catalyst is previously supported on the aggregated
honeycomb structured body 40. Such case will be described using Fig. 2.
First, on a partition wall portion 60 of the honeycomb structured body with an exhaust
gas purifying catalyst 61 supported thereon as shown in Fig. 2(a), when exhaust gases
pass, PM in the exhaust gases is captured and accumulate on the surface of the filter,
as shown in Fig. 2(b). Here, since the supported catalyst and the PM are made into
contact, PM is readily burned according to the effect of the catalyst.
[0072] The captured PM 72 needs to be burned and removed (the filter needs to be subjected
to the regenerating process) periodically, and a post-injection system is mainly used
for such processing.
[0073] When the regenerating process for burning and removing the PM 72 is carried out,
cerium oxides 73 remain with ashes 63, as shown in Fig. 2(c).
When the regenerating process of the filter is repeatedly carried out, the PM 72 and
the cerium oxides 73 are accumulated on the ashes 63, as shown in Fig. 2(d), and the
surface of the exhaust gas purifying catalyst 61 supported on the filter will be covered
with the ashes 63; thus the exhaust gas purifying catalyst 61 supported on the filter
can not be made into contact with the PM 72. Even in such a case, there exists a portion
in which the cerium oxide 73 is exposed in the uppermost surface of the ashes. Since
this cerium oxide 73 can contact with the PM 72, it can function as a catalyst for
promoting burning of the PM. As a result, the burning temperature of the PM can be
lowered and the regeneration rate of the filter improves.
[0074] In the fourth aspect of the present invention, the type of filter for the exhaust
gas purifying device is not particularly limited, and for example, a honeycomb structured
body comprising a plurality of cells formed in the longitudinal direction with a cell
wall therebetween, and a plug for sealing either one of the ends of the cells so that
exhaust gases pass through the cell wall, may be used.
[0075] The above-mentioned honeycomb structured body can be divided generally into types
as follows: a honeycomb structured body in which a plurality of honeycomb fired bodies
having plural cells formed in the longitudinal direction with a cell wall therebetween,
either one of the ends of the cell being sealed with a plug, are bound together through
a sealing material layer (adhesive layer) to form a ceramic block with a sealing material
layer (coat layer) formed on the periphery thereof (herein after, this type is also
referred to as an aggregated honeycomb structured body); and a honeycomb structured
body comprising a single honeycomb fired body in which plural cells are longitudinally
formed with a cell wall therebetween, and with either one of the ends of the cell
being sealed with a plug (hereinafter, this type is also referred to as an integral
honeycomb structured body).
[0076] Fig. 3 is a perspective view that schematically shows one example of the aggregated
honeycomb structured body, Fig. 4(a) is a perspective view showing a honeycomb fired
body that constitutes the honeycomb structured body shown in Fig. 3, and Fig. 3(b)
is a cross-sectional view taken along line B-B of the honeycomb fired body shown in
Fig. 3(a).
[0077] As shown in Fig. 3, in the aggregated honeycomb structured body 40, a plurality of
honeycomb fired bodies 50 made from silicon carbide-based ceramic or the like are
combined with each other through a sealing material layer (adhesive layer) 41 to form
a cylindrical ceramic block 43, and a sealing material layer (coat layer) 42 is formed
on the periphery of this ceramic block 43.
[0078] In the aggregated honeycomb structured body 40 shown in Fig. 3, the shape of the
ceramic block is cylindrical; however, in the honeycomb structured body, the shape
of the ceramic block is not limited to a cylindrical shape as long as it is pillar-shaped
and, for example, it may be a cylindroid shape, a rectangular pillar-shape, or any
other desired shape.
[0079] As shown in Figs. 4(a) and 4(b), the honeycomb fired body 50 has a structure in which
a plurality of cells 51 are placed in parallel with one another in the longitudinal
direction with a cell wall 53 therebetween, with either one of the end portions of
the cell 51 being sealed with a plug 52 and, the cell wall 53 that separates the cells
51 are allowed to function as filters. In other words, each of the cells 51 formed
in the honeycomb fired body 50 has either one of the end portions on the inlet side
or the outlet side of exhaust gases sealed with the plug 52 as shown in Fig. 4(b)
so that exhaust gases that have flowed into one of the cells 51 are always allowed
to flow out of another cell 51 after having passed through the cell wall 53 that separates
the cells 51.
[0080] The aggregated honeycomb structured body 40 is mainly made of porous ceramics, and
with respect to the material, examples thereof include: nitride ceramics such as aluminum
nitride, silicon nitride, boron nitride and titaniumnitrideand the like; carbide ceramics
such as silicon carbide zirconium carbide, titanium carbide, tantalum carbide, tungsten
carbide and the like; and oxide ceramics such as alumina, zirconia, cordierite, mullite,
silica, aluminum titanate and the like. Further, the honeycomb fired body may be formed
by a composite body between silicon and silicon carbide. In the case where the composite
body between silicon and silicon carbide is used, silicon is desirably added thereto
so as to be set to 0 to 45% by weight in the entire body.
In particular, when the aggregated honeycomb structured body is used as a filter,
a silicon carbide-based ceramic material which is superior inheat resistance, mechanical
characteristics and has a high thermal conductivity, is desirably used as the material
of the honeycomb fired body. Here, the silicon carbide-based ceramic refers to a material
having a silicon carbide content of 60% by weight or more.
[0081] With respect to the thickness of the cell wall 53, the lower limit value is desirably
set to 0.1 mm and the upper limit value is desirably set to 0.4 mm.
The thickness of the cell wall 53 being less than 0.1 mm tends to cause a reduction
in strength of the cell wall 53, thereby causing damages such as cracks and the like,
and on the other hand, with the thickness of the cell wall 53 exceeding 0.4 mm, a
high aperture ratio can not be maintained, which tends to cause an increase in the
pressure loss as a result.
[0082] The porosity of the aggregated honeycomb structured body 40 is desirably in the range
of 40 to 60%.
The porosity of less than 40% tends to cause increase in the pressure loss, while
the porosity exceeding 60% tends to cause reduction in strength.
Here, the above-mentioned porosity can be measured through known methods such as a
mercury injection method using a mercury porosimeter, Archimedes method, a measuring
method using a scanning electronic microscope (SEM) and other methods.
[0083] The average pore diameter of the aggregated honeycomb structured body 40 is not particularly
limited, and the lower limit value is desirably set to 1 µm, and the upper limit value
is desirably set to 50 µm. It is more desirable that the lower limit value is set
to 5 µm, and the upper limit value is set to 30 µm. The average pore diameter of less
than 1 µm tends to cause an increase in pressure loss, and on the other hand, with
the average pore diameter exceeding 50 µm, PM readily passes through the pores leading
to insufficient capturing of the PM, which tends to cause a reduction in capturing
efficiency of PM.
[0084] The plug 52 and the cell wall 53 that seal the aggregated honeycomb structured bodies
40 are desirably made from the same porous ceramic material. With this arrangement,
the contact strength between the two members is increased, and by adjusting the porosity
of the plug 52 in the same manner as the cell walls 53, the coefficient of thermal
expansion of the cell walls 53 and the coefficient of thermal expansion of the plug
52 are properly adjusted so that it becomes possible to prevent a gap from being generated
between the plug 52 and the cell walls 53 due to a thermal stress upon production
and in use and also to prevent cracks from occurring in the plug 52 and at portions
of the cell walls 53 that are made in contact with the plug 52.
[0085] With respect to the length of the plug 52, although not particularly limited, in
the case where the plug 52 is made from porous silicon carbide, the lower limit value
is desirably set to 1 mm, and the upper limit value is desirably set to 20 mm.
The length of the plug of less than 1 mm results in cases that the end portion of
the cell can not be sealed surely, while the length exceeding 20 mm tends to reduce
the effective filtration area in the honeycomb structured body.
[0086] In the aggregated honeycomb structured body 40, the sealing material layer (adhesive
layer) 41, which is formed between the honeycomb fired bodies 50, has a function of
preventing exhaust gases from leaking, and further functions as a bonding material
used for binding a plurality of the honeycomb fired bodies 50 to one another. In contrast,
the sealing material layer (coat layer) 42, which is formed on the peripheral face
of the ceramic block 43, is also allowed to function as a sealing material used for
preventing exhaust gases passing through the cells from leaking from the peripheral
face of the ceramic block 43 when the aggregated honeycomb structured body 40 is placed
in an exhaust passage of an engine, and as an reinforcing member for adjusting the
shape of the ceramic block 43 as well as reinforcing the outer periphery thereof.
[0087] Here, in the aggregated honeycomb structured body 40, the adhesive layer 41 and the
coat layer 42 may be formed by using the same material, or may be formed by using
different materials. In the case where the adhesive layer 41 and the coat layer 42
are made from the same material, the compounding ratio of materials thereof may be
the same or different. Moreover, the material may have either a dense structure or
a porous structure.
[0088] With respect to the material used for forming the adhesive layer 41 and the coat
layer 42, not particularly limited, for example, a material, made from an inorganic
binder and an organic binder as well as inorganic fibers and/or inorganic particles,
may be used.
[0089] With respect to the above-mentioned inorganic binder, for example, silica sol and
alumina sol may be used. Each of these materials may be used alone, or two or more
kinds of these may be used in combination. Of the above-mentioned inorganic binders,
silica sol is more desirably used.
[0090] With respect to the organic binder, examples thereof include: polyvinyl alcohol,
methyl cellulose, ethyl cellulose, carboxymethyl cellulose and the like. Each of these
may be used alone or two or more kinds of these may be used in combination. Among
the organic binders, carboxy methyl cellulose is more desirably used.
[0091] With respect to the inorganic fibers, examples thereof include: ceramic fibers such
as alumina, silica, silica-alumina, glass, potassium titanate, aluminum borate and
the like, and whiskers such as alumina, silica, zirconia, titania, ceria, mullite,
silicon carbide and the like. Each of these may be used alone, or two or more kinds
of these maybe used in combination. Among the inorganic fibers, alumina fibers are
more desirably used.
[0092] With respect to the inorganic particles, for example, carbides, nitrides and the
like may be used, and more specifically, inorganic fine powder, made from silicon
carbide, siliconnitride, boron nitride or the like, may be used. Each of these may
be used alone, or two or more kinds of these may be used in combination. Among the
above-mentioned inorganic particles, silicon carbide, which is superior in thermal
conductivity, is more desirably used.
[0093] Moreover, a pore-forming agent, such as balloons that are fine hollow spheres composed
of oxide-based ceramics, spherical acrylic particles and graphite, may be added to
the above-mentioned paste used for forming the sealing material layer, if necessary.
With respect to the above-mentioned balloons, not particularly limited, for example,
alumina balloons, glass micro-balloons, shirasuballoons, flyashballoons (FAballoons),
mullite balloons and the like may be used. Among these, alumina balloons are more
desirably used.
[0094] Further, a catalyst is supported on the aggregated honeycomb structured body. As
the catalyst, for example, a noble metal such as platinum, palladium, rhodium and
the like may be used as a noble metal catalyst, and also an alkali metal, an alkali
earth metal and an oxide may be used. These may also be used in combination.
Moreover, as an oxide catalyst, a metal oxide such as CeO
2 ZrO
2, FeO
2, Fe
2O
3, CuO, CuO
2, Mn
2O
3, MnO and the like, as well as a composite oxide represented by a composition formula
A
nB
1-nCO
3 (wherein A is La, Nd, Sm, Eu, Gd or Y; B is alkali metal or alkali earth metal; and
C is Mn, Co, Fe or Ni) and the like may be used. When the oxide catalyst is supported
on the honeycomb structured body, the catalyst comes into contact with the PM, thereby
reducing the burning temperature of the PM.
[0095] Moreover, when the above-mentioned catalyst is adhered to the aggregated honeycomb
structured body, the catalyst may be adhered thereto after the surface has been preliminarily
coated with a catalyst supporting layer made of alumina or the like. Thus, the specific
surface area of the honeycomb structured body can be enlarged and the dispersivity
of the catalyst can be enhanced, to increase the reaction site of the catalyst. Further,
the catalyst supporting layer can prevent the catalytic metal from sintering.
[0096] Examples of the material for the catalyst supporting layer include oxide ceramics,
such as alumina, titania, zirconia, silica and the like.
[0097] While the present invention can be applied to a honeycomb structured body in which
the catalyst is not previously supported thereon, more desirably the catalyst is to
be supported on the honeycomb structured body. With the catalyst not being previously
supported, the catalytic amount will be insufficient when burning the PM before a
certain amount of catalyst deriving from the engine oil is piled up, and the burning
temperature is thereby increased, causing poor burning efficiency.
[0098] Next, the following description will discuss a manufacturing method of the aggregated
honeycomb structured body.
First, an extrusion-molding process is carried out by using material paste mainly
composed of the above-mentioned ceramic material so that a square-pillar shaped ceramic
molded body is manufactured.
[0099] Although the material paste is not particularly limited, a material paste in which
the porosity of the manufactured honeycomb fired body is set in the range of 40 to
60% is desirably used. For example, a material paste in which a binder, a dispersant
solution and the like is added to powder composed of the ceramics mentioned above
may be used.
[0100] With respect to the particle size of ceramic powder, although not particularly limited,
those which are less susceptible to shrinkage in the succeeding firing process are
desirably used, and for example, those powders, prepared by combining 100 parts by
weight of powders having an average particle diameter about 3 to 70 µm with 5 to 65
parts by weight of powders having an average particle diameter about 0.1 to 1.0 µm,
are preferably used.
Here, the ceramic powder may be subjected to an oxidizing process.
[0101] With respect to the above-mentioned binder, not particularly limited, examples thereof
include: methylcellulose, carboxy methylcellulose, hydroxy ethylcellulose, polyethylene
glycol, phenolic resin, epoxy resin and the like.
In general, the compounding amount of the above-mentioned binder is desirably set
to about 1 to 15 parts by weight with respect to 100 parts by weight of the ceramic
powder.
[0102] With respect to the dispersant solution, not particularly limited, examples thereof
include: an organic solvent such as benzene and the like; alcohol such as methanol
and the like; water, and the like.
An appropriate amount of the above-mentioned dispersant solution is mixed therein
so that the viscosity of the material paste is set within a fixed range.
[0103] These ceramic powder, binder and dispersant solution are mixed by an attritor or
the like, and sufficiently kneaded by a kneader or the like, and then extrusion-molded.
[0104] Moreover, a molding auxiliary may be added to the material paste, if necessary.
With respect to the molding auxiliary, not particularly limited, examples thereof
include ethylene glycol, dextrin, fatty acid, fatty acid soap, polyvinyl alcohol and
the like.
[0105] Moreover, a pore-forming agent, such as balloons that are fine hollow spheres composed
of oxide-based ceramics, spherical acrylic particles and graphite, may be added to
the above-mentioned material paste, if necessary.
With respect to the above-mentioned balloons, not particularly limited, for example,
alumina balloons, glass micro-balloons, shirasuballoons, flyashballoons (FAballoons),
mullite balloons and the like may be used. Among these, alumina balloons are more
desirably used.
[0106] Next, the above-mentioned ceramic molded body is dried by using a drier such as a
microwave drier, a hot-air drier, a dielectric drier, a reduced-pressure drier, a
vacuum drier and a frozen drier so that a ceramic dried body is formed. Thereafter,
a predetermined amount of plug paste, which forms plugs, is injected into the end
portion on the outlet side of the inlet-side group of cells and the end portion on
the inlet side of the outlet-side group of cells so that the cells are sealed.
[0107] With respect to the plug paste, although not particularly limited, such paste as
to set the porosity of a plug produced through the succeeding processes to 30 to 75%
is desirably used, and for example, the same paste as the material paste may be used.
Moreover, in this process, the length of the plug formed through the subsequent processes
can be adjusted by adjusting the amount of the paste to be inserted.
[0108] Next, the ceramic dried body filled with the plug paste is subjected to degreasing
(for example, 200 to 500°C) and firing processes (for example, 1400 to 2300°C) under
predetermined conditions so that a honeycomb fired body 50 constituted by a single
sintered body as a whole, and having a plurality of cells placed in parallel along
the longitudinal direction with a cell wall therebetween, either one of the end portion
of the cell being sealed, can be manufactured.
With respect to the degreasing and firing conditions of the ceramic dried body, it
is possible to apply conditions that have been conventionally used for manufacturing
a filter made from porous ceramics.
[0109] Next, an adhesive paste to form the adhesive layer 41 is applied to each of the side
faces of the honeycomb fired body 50 with an even thickness to form an adhesive paste
layer, and by repeating a process for successively laminating another honeycomb fired
body 50 on this adhesive paste layer, a honeycomb fired body aggregated body having
a predetermined size is manufactured.
In order to obtain space between the honeycomb fired bodies 50, a method in which
a space holding material is attached onto the honeycomb fired body 50 so that plural
honeycomb fired bodies 50 are put together through space holding materials to produce
an aggregated body and thereafter the adhesive paste is injected into the space between
the honeycomb fired bodies 50, may also be applied.
With respect to the material for forming the adhesive paste, since it has already
been explained, explanation thereof is omitted here.
[0110] Next, the aggregated body of the honeycomb fired bodies is heated so that the adhesive
paste layer is dried and solidified to form the adhesive layer 41.
Then, the aggregated body of the honeycomb fired bodies in which a plurality of the
honeycomb fired bodies 50 are bonded to one another through the adhesive layers 41
is subjected to a cutting process by using a diamond cutter and other tools so that
a ceramic block 43 having a cylindrical shape is manufactured.
[0111] By forming a sealing material layer 42 on the periphery of the ceramic block 43 by
using the sealing material paste, an aggregated honeycomb structured body 40 in which
the sealing material layer 42 is formed on the outer peripheral portion of the cylindrical
ceramic block 43 having a plurality of the honeycomb fired bodies 50 bonded to one
another through the adhesive layers 41.
[0112] Thereafter, according to need, a catalyst is supported on the honeycomb structured
body. The supporting process of the catalyst may be carried out on the honeycomb fired
body prior to the formation of the aggregated body.
When supporting the catalyst, desirably, an alumina film having a high specific surface
area is formed on the surface of the honeycomb structured body, and a catalyst such
as a co-catalyst, platinum and the like is adhered to this alumina film.
[0113] With respect to the method for forming the alumina film on the aggregated honeycomb
structured body, for example, a method in which the honeycomb structured body is impregnated
with a solution of a metal compound containing aluminum such as Al(NO
3)
3 and the like and then heated, and a method in which the honeycomb structured body
is impregnated with a solution containing alumina powder and then heated, and other
methods are proposed.
With respect to the method for adhering the co-catalyst, for example, a method in
which the honeycomb structured body is impregnated with, for example, a solution of
metal compound containing a rare earth element and the like such as Ce(NO
3)
3 and the like and then heated, and other methods are proposed.
With respect to the method for adhering the catalyst, for example, a method in which
the honeycomb structured body is impregnated with, for example, a solution of diammine
dinitro platinum nitric acid ([Pt(NH
3)
2(NO
2)
2]HNO
3, platinum concentration: 4.53% by weight) and the like and then heated is proposed.
Moreover, the catalyst may be adhered by using a method in which the honeycomb structured
body is impregnated with a compound containing alumina powder with a catalyst previously
adhered to the alumina particles, and then heated.
[0114] Further, instead of forming the alumina film, oxides may be supported. As the above-mentioned
oxide, examples thereof include a metal oxide such as CeO
2, ZrO
2, FeO
2, Fe
2O
3, CuO, CuO
2, Mn
2O
3, MnO and the like, and a composite oxide represented by a composition formula A
nB
1-nCO
3 (wherein A is La, Nd, Sm, Eu, Gd or Y; B is alkali metal or alkali earth metal; and
C is Mn, Co, Fe or Ni) . Each of these may be used alone, or two or more kinds of
these may be used in combination.
[0115] Next, the integral honeycomb structured body will be described.
The integral honeycomb structured body consists of a honeycomb structured body manufactured
in an integrated form, wherein the whole honeycomb structured body is not bound through
adhesives and the like. Therefore, the integral honeycomb structured body can be considered
as a honeycomb structured body constituted by one of the honeycomb fired bodies which
comprises the aggregated honeycomb structured body. However, its size is the same
as that of the aggregated honeycomb structured body, and its shape is a required shape
as a honeycomb structured body, namely shapes such as a cylindrical shape, cylindroid
shape and the like.
[0116] Consequently, the structure, the required characteristics and the like of the integral
honeycomb structured body is almost the same as that of the aggregated honeycomb structured
body described above, and the manufacturing method thereof is almost the same as the
method for manufacturing the honeycomb fired body. However, a sealing material layer
may also be provided afterwards on the periphery of such a sintered body.
Moreover, the material used for the ceramic preferably is low in coefficient of expansion,
and has difficulty forming cracks and the like and, for example, cordierite, aluminum
titanate and the like is preferably used.
[0117] The aggregated honeycomb structured body and the integral honeycomb structured body
are normally set into a cylindrical metal casing. The material for the metal casing,
for example, may be metals such as stainless steel, iron and the like. The shape of
the metal casing may be a single-type tubiform, or a separable tubiform (for example,
a clamshell-type metal casing and the like) which can be separated into two or more
parts.
EXAMPLES
[0118] The following description will discuss the present invention in detail by means of
examples; however, the present invention is not intended to be limited by these examples.
(Example 1)
(Preparation of engine oil with compound containing metallic element added thereto)
[0119] To 100 parts by weight of commercial engine oil (base oil, commercial mineral oil
(paraffin-based mineral oil), viscosity: 120 mm
2/s•40°C) was added 1 part by weight of cerium (IV) 1,8-naphthalene-dicarboxylate (hereinafter,
referred to also as 1,8-NDCA) (hereinafter, referred to as additive 1) to prepare
a mixed material.
(Production of aggregated honeycomb structured body)
[0120] Coarse powder of α-type silicon carbide having an average particle diameter of 22
µm (7000 parts by weight) and fine powder of α-type silicon carbide having an average
particle diameter of 0.5 µm. (3000 parts by weight) were wet-mixed, and to 10000 parts
by weight of the resulting mixture were added and kneaded 550 parts by weight of an
organic binder (methyl cellulose), 330 parts by weight of a plasticizer (UNILUB, made
by NOF Corp.), 150 parts by weight of glycerin serving as a lubricant and 2000 parts
by weight of water to obtain a mixed composition, and this was then extrusion-molded
to manufacture a raw molded body having a rectangular pillar shape as shown in Fig.
4.
[0121] Next, after the above-mentioned raw molded body had been dried by using a microwave
drier or the like to prepare a ceramic dried body, predetermined cells were filled
with a plug material paste having the same composition as the raw molded body.
After this had been again dried by using a drier, the resulting product was degreased
at 400°C, and fired at 2200°C in a normal-pressure argon atmosphere for 3 hours to
manufacture a honeycomb fired body 50, which was a silicon carbide sintered body with
a porosity of 42% and an average pore diameter of 11 µm, having a size of 34.3 mm
× 34.3 mm × 150 mm, the number of cells 51 (cell density) of 31 pcs/cm
2 (200 pcs/in
2) and a thickness of the cell walls 53 of 0.40 mm.
[0122] By using a heat resistant adhesive paste containing 30% by weight of alumina fibers
having an average fiber length of 20µm, 21% by weight of silicon carbide particles
having an average particle diameter of 0.6 µm, 15% by weight of silica sol, 5.6% by
weight of carboxy methyl cellulose and 28.4% by weight of water, a number of the honeycomb
fired bodies 50 were bonded to one another, and this was dried at 120°C and then cut
by using a diamond cutter so that a cylindrical ceramic block 43 having a thickness
of the adhesive layer of 1 mm was manufactured.
[0123] Next, silica-alumina fibers (average fiber length: 100 µm, average fiber diameter:
10 µm) (23.3% by weight), which served as inorganic fibers, silicon carbide powder
having an average particle diameter of 0.3 µm (30.2% by weight), which served as inorganic
particles, silica sol (SiO
2 content in the sol: 30% by weight) (7% by weight), which served as an inorganic binder,
carboxymethyl cellulose (0.5% by weight), which served as an organic binder, and water
(39% by weight) were mixed and kneaded to prepare a sealing material paste.
[0124] Next, a sealing material paste layer having a thickness of 0.2 mm was formed on the
peripheral portion of the ceramic block 43 by using the above-mentioned sealing material
paste. Further, this sealing material paste layer was dried at 120°C so that a cylindrical
aggregated honeycomb structured body 40 having a size of 143.8 mm in diameter × 150
mm in length (capacity: 2.44 liters) was manufactured.
[0125] Next, the honeycomb structured body was immersed in a solution containing 10 g of
CeO
2, 40 ml of water and an appropriate amount of a pH-adjusting agent for 5 minutes,
and this was then subjected to a firing process at 500°C so that CeO
2 serving as an oxide catalyst was supported thereon.
Here, the apparent density of the honeycomb fired bodies 50 forming the aggregated
honeycomb structured body 40 was 0.49 g/cm
3.
(Assembly of exhaust gas purifying device)
[0126] Moreover, an exhaust gas purifying device used for measuring the regeneration rate
and evaluating the exhaust gas purification performance was assembled by using the
following method.
Fig. 5 is an explanatory drawing of the exhaust gas purifying device.
The exhaust gas purifying device 270 was prepared as a scanning mobility particle
sizer (SMPS) provided with a common-rail-type diesel engine 276 of 2L, an exhaust
gas pipe 277 that allows exhaust gases from the engine 276 to flow therein, a metal
casing 271 that is connected to the exhaust gas pipe 277 and houses the honeycomb
structured body 40, a sampler 278 that samples exhaust gases prior to the flow through
the honeycomb structured body, a sampler 279 that samples exhaust gases after the
flow through the honeycomb structured body, a diluter 280 that dilutes the exhaust
gases that have been sampled by the samplers 278 and 279 and a PM counter 281 (made
by TSI Co., Ltd., aggregated particle counter 3022A-S) that measures the amount of
PM contained in the diluted exhaust gases.
Although the honeycomb structured body used here is not particularly limited, Fig.
5 shows a view in which the aggregated honeycomb structured body 40 was set therein.
[0127] In the present examples, when the exhaust gas purifying device was assembled, an
aggregated honeycomb structured body was used as the honeycomb structured body, and
with a hold-sealing member formed around the outer peripheral portion thereof, set
in the metal casing.
(Evaluation on exhaust gas purifying performance)
[0128] The following description will discuss a sequence of measuring process.
(Measurements of regenerating rate)
[0129] First, the weight a
0 of an aggregated honeycomb structured body with no PM accumulated thereon was measured.
Next, the engine 276 was driven at the number of revolutions of 3000 min
-1 with a torque of 50 Nm for 5 hours so that PM was accumulated on the aggregated honeycomb
structured body. Here, the honeycomb structured body was once taken out, and the weight
b
1 thereof was measured. Thus, the weight x (= b
1 - a
0) of PM accumulated during a driving process at one time was calculated.
Thereafter, the engine was driven under a post-injection system for 7 minutes so that
the aggregated honeycomb structured body was subjected to a regenerating process,
and the weight a
1 of the aggregated honeycomb structured body after the regenerating process was measured.
By using the following calculation equation, the regenerating rate (%) was calculated.

Here, the regenerating rate, calculated after the regenerating process for the first
time, was referred to as the first regenerating rate.
This driving and regenerating process was set as one cycle, and this cycle was repeated
200 times, with engine oil being exchanged for every 5 cycles.
In this case, the weight a
199 of the aggregated honeycomb structured body immediately after the 199th regenerating
process and the weight a
200 of the aggregated honeycomb structured body immediately after the 200th regenerating
process were measured.
Then, in the same manner as the first regenerating rate, by using the following calculation
equation, the regenerating rate (%) was calculated.

The regenerating rate was set as the 200th regenerating rate.
Here, the repeated operations of 200 cycles correspond to the mileage of 100,000 kilometers.
(Example 2)
[0130] The same processes as those of Example 1 were carried out except that the engine
oil was prepared by adding 3% by weight of the additive 1 thereto as the compound
containing a metallic element, and evaluations were conducted on the exhaust gas purifying
performances.
(Example 3)
[0131] The same processes as those of Example 1 were carried out except that the engine
oil was prepared by adding 5% by weight of the additive 1 thereto as the compound
containing a metallic element, and evaluations were conducted on the exhaust gas purifying
performances.
(Example 4)
[0132] The same processes as those of Example 1 were carried out except that the engine
oil was prepared by adding 10% by weight of the additive 1 thereto as the compound
containing a metallic element, and evaluations were conducted on the exhaust gas purifying
performances.
(Examples 5 to 25)
[0133] The same processes as those of Example 1 were carried out except that each of compounds
indicated by chemical formulas shown in Table 1 was used as the compound containing
a metallic element and that the engine oil was prepared by adding 5% by weight of
each of the additives thereto, and evaluations were conducted on the exhaust gas purifying
performances.
Here, in Table 1, (1,8-C
10H
6O
2)
2Ce of Example 8 represents a metal complex (cerium (IV)1,8-naphthalenediolate) composed
of two molecules of 1,8-naphthalenediolate and cerium (IV).
Moreover, (C
5H
5)
2 in Examples 23 to 25 refers to a (bis) cyclopentadienyl group, and additives used
in Examples 23 to 25 represent cyclopentadienyl complexes of cerium (III), iron (II)
and cobalt (II), respectively.
(Comparative Example 1)
[0134] The same processes as those of Example 1 except that engine oil to which no additive
composed of a compound containing a metallic element was added was used, and evaluations
were conducted on the exhaust gas purifying performances.
(Reference Example 1)
[0135] The same processes as those of Example 1 were carried out except that the engine
oil was prepared by adding 0.5% by weight of the additive 1 thereto as the compound
containing a metallic element, and evaluations were conducted on the exhaust gas purifying
performances.
[0136] Table 1 shows the results of these examples and comparative examples.
[0137]
Table 1
| |
Type of additive containing a metallic element |
Amount of additive (% by weight) |
First regenerating rate (%) |
200th regenerating rate (%) |
| Example 1 |
(1,8-NDCA)2Ce |
1 |
94 |
88 |
| Example 2 |
(1,8-NDCA)2Ce |
3 |
94 |
91 |
| Example 3 |
(1,8-NDCA)2Ce |
5 |
95 |
93 |
| Example 4 |
(1,8-NDCA)2Ce |
10 |
95 |
93 |
| Example 5 |
(1,8-NDCA)Co |
5 |
92 |
88 |
| Example 6 |
(1,8-NDCA)2Mn |
5 |
91 |
86 |
| Example 7 |
(1,8-NDCA) Ni |
5 |
92 |
87 |
| Example 8 |
(1,8-C10H6O2)2Ce |
5 |
94 |
92 |
| Example 9 |
Ce(CH3-CO-CH=CO-CH3)3 |
5 |
93 |
91 |
| Example 10 |
Ce(CH3-CO-CH=CO-OCH3)4 |
5 |
92 |
87 |
| Example 11 |
Ce(O-iso-C3H7)3 |
5 |
92 |
88 |
| Example 12 |
Ce(OCH3) (OC2H5) (O-iso-C3H7) |
5 |
90 |
87 |
| Example 13 |
Ce(O-iso-C3H7)2(CH3-CO-CH=COCH3)2 |
5 |
91 |
87 |
| Example 14 |
Cu(CH3-CO-CH=CO-CH3)2 |
5 |
90 |
86 |
| Example 15 |
Pb(CH3-CO-CH=CO-CH3)2 |
5 |
92 |
87 |
| Example 16 |
Ni(CH3-CO-CH=CO-CH3)2 |
5 |
90 |
86 |
| Example 17 |
V(CH3-CO-CH=CO-CH3)3 |
5 |
91 |
87 |
| Example 18 |
Cr(CH3-CO-CH=CO-CH3)3 |
5 |
92 |
88 |
| Example 19 |
Mn(CH3-CO-CH=CO-CH3) |
5 |
90 |
86 |
| Example 20 |
Fe(CH3-CO-CH=CO-CH3 |
5 |
92 |
87 |
| Example 21 |
Co(CH3-CO-CH=CO-CH3)3 |
5 |
91 |
87 |
| Example 22 |
Sn(CH3-CO-CH=CO-CH3)2 |
5 |
92 |
88 |
| Example. 23 |
(C5H5)2CeH |
5 |
93 |
91 |
| Example 24 |
(C5H5)2Fe |
5 |
94 |
86 |
| Example 25 |
(C5H5)2Co |
5 |
93 |
88 |
| Comparative Example 1 |
Not added |
None |
94 |
62 |
| Reference Example 1 |
(1,8-NDCA)2Ce |
0.5 |
95 |
82 |
(1,8-NDCA): 1,8-naphthalenedicarboxylate group
(1,8-C10H5O2)2Ce2: cerium(IV)1,8-naphthalenediolate
(C5H5)2: (bis)cyclopentadienyl group |
[0138] As clearly indicated by the results shown in Table 1, even after the 200th regenerating
process, the honeycomb structured bodies according to the examples made it possible
to maintain a high regenerating rate of 86% or more, which was almost equal to the
first regenerating process.
[0139] In contrast, in the honeycomb structured body according to Comparative Example 1
although a high regenerating rate was obtained after the first regenerating process,
the regenerating rate after the 200th regenerating process was lowered to a level
of 60%, which was inferior to the regenerating rate of Examples 1 to 25.
The reason for this is presumably because, since no catalyst exists in accumulated
ashes, it is not possible to promote the burning of PM by using the catalyst to fail
to sufficiently remove the PM.
BRIEF DESCRIPTION OF THE DRAWINGS
[0140]
Fig. 1 is a view that schematically shows one part of a diesel engine, and an exhaust
gas purifying device connected to the diesel engine.
Figs. 2(a) to (d) are schematic diagrams that schematically show various states which
occur at a partition wall portion of a honeycomb structured body when the exhaust
gas purifying filter comprising the honeycomb structured body is arranged in a pipe
connected to the engine in the fourth aspect of the present invention.
Fig. 3 is a perspective view that schematically shows one example of the aggregated
honeycomb structured body.
Fig. 4(a) is a perspective view that schematically shows honeycomb fired bodies that
form the honeycomb structured body shown in Fig. 3; and Fig. 4(b) is a cross-sectional
view taken along line B-B thereof.
Fig. 5 is an explanatory drawing that shows the exhaust gas purifying device that
has been assembled in Examples.
Figs. 6(a) to (d) are schematic diagrams that schematically show various states which
occur at a partition wall portion of a honeycomb structured body when the exhaust
gas purifying filter comprising the honeycomb structured body is arranged in a pipe
connected to the engine in the prior art structure.
EXPLANATION OF SYMBOLS
[0141]
- 23, 271
- Metal casing
- 24
- Introducing pipe
- 25
- Exhaust pipe
- 40
- Aggregated honeycomb structured body
- 50
- Honeycomb fired body
- 51
- Cell
- 53
- Cell wall
- 60
- Partition wall portion
- 61
- Exhaust gas purifying catalyst
- 62, 72
- PM
- 63
- Ash
- 73
- Cerium oxide
- 81, 276
- Diesel engine
- 92
- Engine oil
- 93
- Combustion chamber
- 200, 270
- Exhaust gas purifying device