Title of Invention

CATALYST WITH IMPROVED LIGHTOFF PERFORMANCE

Abstract A catalyst for the cleaning of the exhaust gases of internal combustion engines, comprising a honeycomb composed of smooth and corrugated metal sheets with an entrance end face and an exit end face for the exhaust gases, the metal sheets being provided with holes to reduce their heat capacity and a catalyst material having been applied to the metal sheets, characterized in that the holes of the metal sheets are completely filled with catalyst material and the hole area of all holes together is 5 to 80% of the area of the metal sheets.
Full Text

Catalyst with improved lightoff performance
Description
The present invention addresses metallic honeycombs as
supports for a coating of catalyst material for the
exhaust gas cleaning of internal combustion engines.
What is desired from the honeycombs is firstly a large
geometric surface area to accommodate the coating and
secondly a low heat capacity in order that the
honeycomb warms up rapidly to the operating temperature
of the catalyst. In addition, a sufficient mechanical
stability is required from the honeycombs in order to
withstand the mechanical stresses through the pulsating
gas flow and the vibrations of engine and vehicle.
Moreover, the material of the honeycomb has to be
resistant to the corrosive exhaust gas atmosphere at
high temperatures.
The catalytic coating of a finished catalyst consists
of finely divided thermally stable metal oxides on
whose surface are deposited catalytically active
platinum group metals. Suitable metal oxides are, for
example, aluminum oxide, titanium oxide, silicon oxide,
cerium oxide, zirconium oxide, zeolites and mixtures or
mixed oxides thereof, and stabilizers such as lanthanum
oxide and barium oxide. To apply these materials to the
honeycomb, the pulverulent materials are, for example,
suspended in water. Subsequently, this coating
suspension is deposited onto the honeycombs by known
processes, dried and consolidated by calcining.
The honeycombs may be of different structure. Even at a
very early stage, spiral-wound honeycombs were used.
They consist of one smooth and one corrugated sheet
layer which, are placed one on top of another and then
wound up in a spiral and inserted into an outer tube.

The two sheet layers form channels through which the
exhaust gas can flow and enter into intensive contact
with the catalytic coating.
In another design, the honeycomb is formed from a
multitude of smooth and corrugated sheet layers, or
differently corrugated sheet layers, arranged in
alternation, in which case the sheet layers first form
one or more stacks which are intertwined with one
another. The ends of the sheet layers are -on the
outside and can be bonded with an outer tube. This
forms many connections between sheet layers and outer
tube, which increase the mechanical strength of the
honeycomb.
The material used for the sheet layers are preferably
aluminum-containing steel alloys, which are marketed,
for example, under the trade name FeCrAlloy®. This is
an iron-chromium-aluminum alloy. The thickness of' the
sheet layers is usually between 20 and 80 µm,
preferably 50 µm.
It has been known for some time that the sheet layers
can be provided with perforations and corrugations in
order to influence the flow within the channels and/or
to achieve transverse mixing between the individual
flow channels. It is likewise known that slotted sheets
can be used for the construction of metallic
honeycombs. US 5,599,509 proposes, for example,
equipping the sheets with slots transverse to the flow
direction of the exhaust gas in the entrance region of
the honeycomb in order to reduce the heat capacity of
the honeycomb in this region in a controlled manner.
As a result of the reduced thermal conductivity and
heat capacity in the front part, the catalyst coating
applied reaches its lightoff temperature more rapidly
and hence also achieves a better conversion, for

example for carbon monoxide and hydrocarbons. However,
the improvement in the conversion depends significantly
upon the percentage slot area of the sheet layers. The
conversion is improved only within a range of slot
areas between 20 and 50%. Above 50%, the hydrocarbon
conversion decreases again because the catalyst
material available decreases with increasing slot area
and equal thickness of the catalyst layer. The
improvements in the conversion are therefore observed
only in the warm up phase. After the warmup phase, the
reduced amount of catalyst material leads to a worsened
conversion of the harmful substances in the exhaust
gas. Moreover, such a catalyst, owing to the small
amount of catalyst material, has a low aging
resistance. Furthermore, the perforation in the sheet
layers increases the back pressure of the catalyst,
since turbulence forms at the holes. If the intention
were to apply the same mass of catalyst material as in
the case of an unperforated support with the same
geometry to such a catalyst support, the layer
thickness of the catalyst layer and hence likewise the
back pressure of the catalyst would inevitably
increase.
DE 103 14 085 A1 likewise describes metallic honeycombs
composed of at least partly perforated sheet layers.
The aim of the perforations is to enable transverse
mixing of the exhaust gas streams of different flow
channels. In the coating, it is therefore ensured that
the holes are not closed by the coating suspension. For
this reason, the honeycombs are coated in a vibration
unit which generates a relative motion between the
coating suspension and the support body and hence
prevents closure of the holes.
US 5,821,194 describes a metallic honeycomb composed of
smooth and corrugated sheet layers. To improve the
adhesion of a pre-coating material, the sheet layers

are equipped with a multitude of holes, into which the
pre-coating composition penetrates in the course of
coating and forms a mechanical anchor between sheet
layers and coating material. For this purpose, the
diameter of the holes is about half the size of the
thickness of the sheet layers and is thus from 25 to
35 µm. The holes are arranged at a distance of about
1 mm from one another.
The present invention shall avoid the disadvantages
known from the prior art of perforated sheet layers. It
is an object of the invention to compensate for the
loss of support surface through the hole surface of the
sheet layers by means of suitable measures.
This object is achieved by a catalyst for the cleaning
of the exhaust gases of internal combustion engines,
which comprises a honeycomb composed of smooth and
corrugated metal sheets with an entrance end face and
an exit end face for the exhaust gases, the metal
sheets being provided with holes to reduce their heat
capacity and a catalyst material having been applied to
the metal sheets. The catalyst is characterized in that
the holes and/or slots of the metal sheets are filled
substantially with catalyst material and the hole area
of all holes together is 5 to 80% of the area of the
metal sheets.
In contrast to US 5,599,509, the holes and slots in the
sheet layers according to the present invention are
filled with catalyst material. The filling with
catalyst material or with a pre-coating is effected
directly in the coating operation; no additional
working steps are required. When the same amount of
catalyst material is used as finds use in the case of
supports of the same geometry without perforations, the
heat capacity is reduced by the proportion of the

perforations in the sheet layers. The physical data in
Table 1 can serve to estimate these effects:
Table 1: Physical data of FeCrAlloy and catalyst layer
composed of aluminum oxide in comparison

The advantage according to the invention is that the
perforations of the sheet layers do not lead to a
reduction in the amount of catalyst material. As a
consequence, the inventive catalyst, as a result of the
reduced heat capacity of the support, reaches its
lightoff temperature very rapidly and then displays the
full activity of the unreduced amount of catalyst
coating. Furthermore, the inventive catalyst, owing to
the higher loading concentration with catalyst
material, has an improved aging stability over
conventional perforated catalysts.
Of course, it would also be possible to apply the same
coating concentration in accordance with the prior art
without closing the holes on the honeycomb. However,
the coating thickness would then inevitably be
significantly greater and would thus lead to a higher
flow resistance of the catalyst.
To prepare the inventive catalyst, the properties of
the coating suspension have to be adjusted to the hole
dimensions in order to ensure complete filling of
substantially all holes with catalyst material. Low
viscosity coating suspensions can close only small
holes; viscous coating suspensions, in contrast, cover
even relatively large holes. The person skilled in the

art can easily determine the optimal conditions by a
few preliminary experiments.
The shape of the holes need not be circular. The hole
area coverable by the coating suspension is dependent
upon the type of holes and the properties of the
coating suspension. Generally, the area of the
individual holes may be from 0.1 to 25 mm2. In the case
of circular holes, a hole area of from 0.1 up to 1 mm2
has been found to be useful; in the case of elongated
holes, the hole area, in contrast, may be selected
between 0.25 and 25 mm2, preferably between 0.25 and
5 mm2. Within the context of the restrictions
mentioned, the holes can therefore be round,
elliptical, oval, square, rectangular, slot-shaped or
polygonal.
When the above requirements with regard to the
properties of the coating suspension and the hole
dimensions are observed, the known coating processes by
dipping, pouring-over, sucking-in or pumping-in may be
employed for the actual coating operation. In the
removal of excess coating suspension by blowing with
compressed air, it must, though, be ensured that the
holes closed with the moist catalyst material are not
opened again in this operation.
After the coating suspension has been dried, it is
calcined at from about 300 to 600°C. Thereafter, the
holes are closed with a robust layer of the catalyst
material which withstands the harsh operating
conditions in the exhaust gas line of an internal
combustion engine.
In this way, as in the case of unperforated honeycombs,
according to the coating thickness desired, it is
possible to achieve coating concentrations between 50
and 400 grams per liter of volume of the honeycomb. If

the intention were to apply the same coating
concentration without closing the holes, the coating
thickness on the sheets would have to be increased
correspondingly.
For the production of the honeycomb, preference is
given to using all sheet layers, both the smooth and
the corrugated sheet layers, in perforated form. The
advantages of the invention are, though - even if in
attenuated form - also realized when, for example, only
the smooth or only the corrugated sheet layers are used
in perforated form.
Furthermore, it may be appropriate to restrict the
perforations only to a particular region of the
honeycomb. It is advantageous, for example, to position
the perforations only in the inflow region of the
honeycomb.
The area of all holes together relative to the total
area A of the sheet layers in the perforated region
determines the achievable reduction in the heat
capacity. According to the invention, the area of all
holes relative to the total area in the perforated
region of the honeycomb is between 5 and 80%. Above
80%, the strength of the honeycomb is too greatly
impaired by the perforations. The hole fraction is
preferably between 5 and 65%, in particular between 20
and 65%.
In addition to the perforations, the sheet layers may
also have corrugations and embossments when the exhaust
gas stream is to be swirled to improve the contact with
the catalytic coating.
It has been found to be particularly advantageous to
use so-called expanded metals for the sheet layers to
construct the honeycomb. An expanded metal refers to a

metal sheet with orifices, known as meshes, which are
obtained by offset cuts with simultaneous stretching at
right angles to the cuts without material loss. The
expanded metal has a lattice structure with rhombus-
shaped or slot-shaped meshes. The meshes consist of
strands and the orifice enclosed by them. The crossing
points of the strands are referred to as node points.
The size of a mesh is given by mesh length and mesh
width. The mesh length is the distance from node point
center to node point center in the direction of the
long diagonal. The same applies to the mesh width. A
further characteristic of expanded metals is the width
of their strands.
In the production of expanded metal from a metal sheet,
the width of the metal sheet at right angles to the
stretching direction is maintained, since the strands
are elongated in the punching step because the as yet
unpunched sheet resists deformation before the punching
step. This forms a corrugated, plastically structured
surface of the expanded metal. When a smooth surface is
desired, the expanded metal can be rolled flat after
the stretching. An expanded metal can be produced with
a free cross-sectional area between 4 and about 90%.
For the inventive catalyst, the smooth or corrugated
metal sheets or both sheet types may consist of an
expanded metal. The mesh length is preferably between
0.5 and 5 mm with stretching between 5 and 80%,
preferably between 10 and 50%. Good results are
achieved with an expanded metal with stretching of 30%.
Stretching of 30% means that the expanded metal, after
production, has 1.3 times the length of the starting
sheet. Such a sheet thus has a free hole area of about
23% and a mass reduced by this percentage compared to a
conventional sheet of the same length.

The corrugated surface of the expanded metal has an
advantageous effect on the catalytic action of the
finished catalyst, since it swirls the exhaust gas
within the flow channels of the catalyst and hence
improves the contact with the catalyst coating.
However, it increases the exhaust gas back pressure.
When this is not desired, the expanded metals can be
flattened by rolling before the catalyst body is
formed.
The inventive catalysts are used for cleaning the
exhaust gas of internal combustion engines. The
catalytic coating may be adjusted to the specific
requirements of the exhaust gas composition. The
coating may comprise an oxidation catalyst, three-way
catalyst, nitrogen oxide storage catalyst or SCR
catalyst. The inventive catalyst can be used in motor
vehicles with gasoline or diesel engines, both as a
starting catalyst close to the engine or as an
underfloor catalyst. The catalyst is particularly
advantageous for cleaning the exhaust gas of motorized
bicycles and water vehicles.
Figures 1 to 7 serve to further illustrate the
invention. They show:
Figure 1 to 4: examples of perforated sheet layers with
different hole shapes and hole
proportions
Figure 5: example of the improved lightoff of the
catalyst
Figure 6: photographs of an expanded metal with a
stretching of 30% used to form a
honeycomb
a) in the uncoated state
b) after catalytic coating

Figure 7: comparative measurement of the exhaust
gas emission in the European motorcycle
test cycle with a conventional honeycomb
composed of unperforated sheet layers
and an inventive honeycomb with sheet
layers manufactured from an expanded
metal
Figures 1 to 4 show a few examples of possible
perforations of the sheet layers in a scale diagram
with twofold magnification.
Figures 1 and 2 show perforations composed of circular
holes with a diameter of 0.8 mm. The perforations of
Figures 1 and 2 differ by the distance of the holes
from one another and the percentage hole area which is
different as a result. According to Figure 1, the hole
area is 50% of the perforated sheet region, while the
hole area' is only 25% according to the perforation of
Figure 2.
Figures 3 and 4 show perforations with elongated holes
of different size and percentage hole area.
Simulation calculations
To demonstrate the advantages of the inventive
catalyst, simulation calculations were undertaken. As
the basis for the simulations, the exhaust gas values,
i.e. harmful substance concentrations and exhaust gas
temperature, of a motorcycle with a 1200 cm3 four-
stroke engine were measured in the EU3 test cycle as a
function of test time.
For the calculation of the harmful substance
conversion, two metal honeycombs with a cell density of
360 cm-2, a diameter of 90 mm and a length of 74.5 mm

were assumed. The metal sheets consisting of FeCrAlloy
had a thickness of 50 µm. For a comparative
calculation, it was assumed that the honeycomb is
constructed from unperforated metal sheets, while, for
the example calculation, it was assumed that the
honeycomb has perforated metal sheets with a hole area
of 50%. The catalyst coating specified was a three-way
catalyst with platinum, palladium and rhodium with a
noble metal concentration of 1.48 g/1 of honeycomb
volume, equal in both cases.
The results of the measurements and calculations are
shown in Figure 5 for the first 200 seconds of the EU3
cycle. "V" denotes the speed profile of the motorcycle
according to the test cycle. T1 is the measured
temperature profile of the exhaust gas before entry
into the catalyst.
Curve T2 in Figure 5 shows the calculated temperature
profile behind the unperforated comparative catalyst,
while curve T3 shows the temperature profile behind the
perforated example catalyst. It can be seen clearly
that, owing to the perforation of the example catalyst,
it heats significantly more rapidly. Thus, the
perforated catalyst reaches a temperature of 250°C at
At = 13 s earlier than the unperforated comparative
catalyst.
Example 1: Comparative catalyst (catalyst A):
A cylindrical metal honeycomb composed of unperforated
metal foils of 0.05 mm thickness, a diameter of 90 mm,
a length of 74.5 mm and a cell density of 200 cm-2 was
coated with a conventional three-way catalyst
comprising platinum, palladium and rhodium with a noble
metal concentration of 1.55 g/1 of honeycomb volume.
Example 2: Inventive catalyst (catalyst B):

For comparison of the catalytic properties, a further
supported metal catalyst with the same dimensions, foil
thicknesses and the same cell density as the
comparative catalyst was produced. Instead of
unperforated metal foils, however, an expanded metal
with a stretching of 30% and a mesh length of 0.6, a
mesh width of 0.5 and a strand width of 0.18 mm was
used. The metal support was coated with the same three-
way catalyst in the same concentration as the
comparative catalyst.
Figure 6 a) shows a photograph of the structure of the
expanded metal used prior to catalytic coating.
Figure 6 b) shows a corresponding photograph after
catalytic coating. It can be seen clearly that the mesh
orifices of the expanded metal have been filled
completely with catalyst material. The catalyst
material adhered in an outstanding manner on the
expanded metal and showed no detachment even in the
case of blowing with compressed air and knocking.
Back pressure measurements:
Owing to its three-dimensionally structured surface,
the inventive catalyst support B without coating
The back pressure of the two supported metal catalysts
was determined prior and after catalytic coating with a
mass flow rate of 300 m3 (STP)/h (m3 (STP) = standard
m3). The results are reproduced in Table 2 below.


exhibits a significantly higher back pressure than the
metal support comprising the unperforated metal foils.
After the catalyst coating has been applied, the back
pressure of the comparative catalyst increases by 58%
from 5.9 to 9.4 mbar. In the case of the inventive
catalyst support composed of expanded metal foils, the
back pressure after the coating increases only by 22%
from 8.2 to 10.1 mbar. The surprising result is found
here that by filling of the meshes of the expanded
metal with catalyst material the back pressure
difference becomes negligible between the two catalysts
compared to the back pressure increase between uncoated
and coated catalyst support.
Measurement of the exhaust gas emissions in the
European motorcycle test cycle:
Catalysts A and B were analyzed on a motorcycle with
regard to their exhaust gas emissions in the European
motorcycle test cycle. Figure 7 shows the measurements
of the CO, HC and NOx emissions of the two catalysts
accumulated during the test as a function of driving
time. Figure 7 also shows the speed at which the
motorbike traveled. The emission curves of the
inventive catalyst B for carbon monoxide and
hydrocarbons are significantly below the curves for
comparative catalyst A. The difference in the emission
between the two catalysts is attributable to the cold-
start phase over the first 100 seconds and the reason
for it is the shorter lightoff time of the inventive
catalyst owing to its lower thermal mass. After the
cold-start phase, the two catalysts convert the harmful
substances equally well, since they are coated with the
same amount of catalyst material. As a consequence, the
emission curves run parallel to one another after the
cold-start phase.

Table 3 lists the constant volume sampling results for
the harmful substances during this test.

The results of Table 3 show that the inventive catalyst
B, based on the comparative catalyst, has an emission
of carbon monoxide reduced by 19%, an emission of THC3
reduced by 31% and an emission of nitrogen oxides
reduced by 19%.

WE CLAIM:
1. A catalyst for the cleaning of the exhaust gases of internal combustion
engines, comprising a honeycomb composed of smooth and corrugated
metal sheets with an entrance end face and an exit end face for the
exhaust gases, the metal sheets being provided with holes to reduce their
heat capacity and a catalyst material having been applied to the metal
sheets, characterized in that the holes of the metal sheets are completely
filled with catalyst material and the hole area of all holes together is 5 to
80% of the area of the metal sheets.
2. The catalyst as claimed in claim 1, wherein the holes have a round,
elliptical, oval, square, rectangular, slot-shaped or polygonal cross section.
3. The catalyst as claimed in claim 2, wherein the holes have an area
between 0.1 mm2 to 25 mm2.
4. The catalyst as claimed in claim 3, wherein the holes are positioned over
the entire surface or over part of the surface of the metal sheets.
5. The catalyst as claimed in claim 1, wherein the smooth or the corrugated
metal sheets or both metal sheets are formed from expanded metal, the
expanded metal having a mesh length from node center to node center
between 0.5 and 5 mm.
6. The catalyst as claimed in claim 5, wherein the elongation of the
expanded metal is selected from the range between 5 and 80%.

7. The catalyst as claimed in claim 6, wherein the expanded metal has been
rolled flat after its production.
8. The catalyst as claimed in claim 5, wherein the mesh of the expanded
metal is positioned over the entire surface or over part of the surface of
the expanded metal.
9. The catalyst as claimed in claim 1, wherein it has a loading with catalyst
material in a concentration between 50 and 400 g/1 of volume of the
honeycomb.



ABSTRACT


Title: Catalyst with improved lightoff performance
A catalyst for the cleaning of the exhaust gases of internal combustion engines,
comprising a honeycomb composed of smooth and corrugated metal sheets with
an entrance end face and an exit end face for the exhaust gases, the metal
sheets being provided with holes to reduce their heat capacity and a catalyst
material having been applied to the metal sheets, characterized in that the holes
of the metal sheets are completely filled with catalyst material and the hole area
of all holes together is 5 to 80% of the area of the metal sheets.

Documents:

3145-KOLNP-2008-(15-10-2013)-ABSTRACT.pdf

3145-KOLNP-2008-(15-10-2013)-ANNEXURE TO FORM 3.pdf

3145-KOLNP-2008-(15-10-2013)-CLAIMS.pdf

3145-KOLNP-2008-(15-10-2013)-CORRESPONDENCE.pdf

3145-KOLNP-2008-(15-10-2013)-FORM-1.pdf

3145-KOLNP-2008-(15-10-2013)-FORM-2.pdf

3145-KOLNP-2008-(15-10-2013)-OTHERS.pdf

3145-KOLNP-2008-(15-10-2013)-PA.pdf

3145-KOLNP-2008-(15-10-2013)-PETITION UNDER RULE 137.pdf

3145-kolnp-2008-abstract.pdf

3145-KOLNP-2008-CANCELLED PAGES.pdf

3145-kolnp-2008-claims.pdf

3145-KOLNP-2008-CORRESPONDENCE 1.1.pdf

3145-KOLNP-2008-CORRESPONDENCE-1.2.pdf

3145-KOLNP-2008-CORRESPONDENCE-1.3.pdf

3145-kolnp-2008-correspondence.pdf

3145-kolnp-2008-description (complete).pdf

3145-kolnp-2008-drawings.pdf

3145-KOLNP-2008-EXAMINATION REPORT.pdf

3145-kolnp-2008-form 1.pdf

3145-KOLNP-2008-FORM 18-1.1.pdf

3145-KOLNP-2008-FORM 18.pdf

3145-kolnp-2008-form 2.pdf

3145-KOLNP-2008-FORM 26.pdf

3145-kolnp-2008-form 3.pdf

3145-kolnp-2008-form 5.pdf

3145-KOLNP-2008-GRANTED-ABSTRACT.pdf

3145-KOLNP-2008-GRANTED-CLAIMS.pdf

3145-KOLNP-2008-GRANTED-DESCRIPTION (COMPLETE).pdf

3145-KOLNP-2008-GRANTED-DRAWINGS.pdf

3145-KOLNP-2008-GRANTED-FORM 1.pdf

3145-KOLNP-2008-GRANTED-FORM 2.pdf

3145-KOLNP-2008-GRANTED-FORM 3.pdf

3145-KOLNP-2008-GRANTED-FORM 5.pdf

3145-KOLNP-2008-GRANTED-SPECIFICATION-COMPLETE.pdf

3145-KOLNP-2008-INTERNATIONAL EXM REPORT.pdf

3145-KOLNP-2008-INTERNATIONAL PUBLICATION-1.1.pdf

3145-kolnp-2008-international publication.pdf

3145-KOLNP-2008-INTERNATIONAL SEARCH REPORT & OTHERS-1.2.pdf

3145-KOLNP-2008-INTERNATIONAL SEARCH REPORT 1.1.pdf

3145-kolnp-2008-international search report.pdf

3145-KOLNP-2008-OTHERS-1.1.pdf

3145-KOLNP-2008-OTHERS.pdf

3145-kolnp-2008-pct request form.pdf

3145-KOLNP-2008-PETITION UNDER RULE 137.pdf

3145-KOLNP-2008-REPLY TO EXAMINATION REPORT.pdf

3145-kolnp-2008-specification.pdf

3145-KOLNP-2008-TRANSLATED COPY OF PRIORITY DOCUMENT.pdf

abstract-3145-kolnp-2008.jpg


Patent Number 261146
Indian Patent Application Number 3145/KOLNP/2008
PG Journal Number 24/2014
Publication Date 13-Jun-2014
Grant Date 06-Jun-2014
Date of Filing 31-Jul-2008
Name of Patentee UMICORE AG & CO. KG
Applicant Address RODENBACHER CHAUSSEE 4, 63457 HANAU-WOLFGANG
Inventors:
# Inventor's Name Inventor's Address
1 QUELL, JUERGEN HAUPTSTRASSE 117, 67126 HOCHDORF-ASSENHEIM
PCT International Classification Number F01N 3/28
PCT International Application Number PCT/EP2007/001023
PCT International Filing date 2007-02-07
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 10 2006 005 788.0 2006-02-07 Germany