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Chang H. KIM, et al.
Perovskite-Strontium Catalyst
http://sprint.usatoday.mlogic3g.com/1591293/news/
Mar 26 2010
New
catalytic converter material could make for cleaner, cheaper cars
by
Elizabeth Weise
Imagine a fuel-efficient, clean-burning diesel engine that costs $1,000
to $5,000 less than those built today. That's the possibility raised by
research published this week in the journal Science, from chemical
engineers at GM who've found a way to substitute a cheap mineral for
wedding-ring-quality metals in catalytic converters.
The GM chemists found a way to use a mineral called perovskite, doped
with strontium, in place of the expensive precious metals. It's
something of a holy grail in the industry, which many groups have been
working on for the past 15 years. While the GM scientists were focusing
on diesel engines, their technology should also work in gasoline
engines.
"It's an order of magnitude cheaper," says Chang Hwan Kim, a chemical
engineer at GM's technology center in Warren, Mich. and the senior
author on the paper.
"It's a really significant step forward," says Charles Peden, a chemist
and director of the Institute for Interfacial Catalysis at the Pacific
Northwest National Laboratory in Richland, Wash. "The high cost of
platinum is really causing problems for these new emissions control
technologies."
Getting cars today to be both fuel efficient and low-emission is a
difficult trade-off.
To make a car fuel efficient, you want to get a mix of air and fuel
that burns as much of the fuel as possible. But to put out few
pollutants, the current catalyst technology requires that not all the
fuel is burned. "The catalytic converter doesn't work if it doesn't
have enough unburnt fuel," says Peden.
The catalytic converter changes the smog-creating chemicals nitrogen
oxide and nitrogen dioxide put out by the engine into harmless nitrogen.
To cut down on smog car companies began adding catalytic converters to
their products in the 1970s. Those catalytic converters used
precious metals such as platinum, palladium and rhodium as catalysts,
to speed up the conversion of the nitrogen oxide and nitrogen dioxide
into plain nitrogen. It's this technology that's decreased air
pollution from cars tremendously over the past 15 years. But it's also
raised their price.
Newer catalytic converters require less unburnt fuel to work, but in
order to do so they require a lot more platinum or other precious
metals. And with prices going up, that's been a huge headache for auto
manufacturers.
"There are still a few things we have to work on to develop this as a
commercial product, but we were very excited," says Kim.
Science 327(5973):1624-7 ( Mar 26,
2010 )
Strontium-doped
perovskites rival platinum catalysts for treating NOx in simulated
diesel exhaust.
Kim CH, Qi G, Dahlberg K, Li W
The high cost and poor thermal durability of current lean nitrogen
oxides (NOx) aftertreatment catalysts are two of the major barriers to
widespread adoption of highly fuel-efficient diesel engines. We
demonstrated the use of strontium-doped perovskite oxides as efficient
platinum substitutes in diesel oxidation (DOC) and lean NOx trap (LNT)
catalysts. The lanthanum-based perovskite catalysts coated on monolith
substrates showed excellent activities for the NO oxidation reaction, a
critical step that demands heavy usage of platinum in a current diesel
aftertreatment system. Under realistic conditions, La(1-x)SrxCoO3
catalysts achieved higher NO-to-NO2 conversions than a commercial
platinum-based DOC catalyst. Similarly, a La(0.9)Sr(0.1)MnO3-based LNT
catalyst achieved NOx reduction performance comparable to that of a
commercial platinum-based counterpart. The results show promise for a
considerably lower-cost diesel exhaust treatment system.
Patents
for Perovskite-Strontium Applications
Cellular ceramic type catalyst for
catalytic combustion of perovskite as well as preparation and
application thereof
CN101439290
Inventor(s): YINFEI CHEN [CN]; HANFENG LU [CN];
HAIFENG HUANG [CN]; HUAYAN LIU [CN]; FANG GUAN [CN] + (CHEN YINFEI, ;
LU HANFENG, ; HUANG HAIFENG, ; LIU HUAYAN, ; GUAN FANG)
Abstract -- The invention
discloses a honeycomb ceramics perovskite catalytic combustion
catalyst; the honeycomb ceramics with a metal oxide coating is used as
a carrier; the catalytic activity components disclosed in formula (I)
are loaded; wherein, La, Sr, Co, and Mn respectively represent
lanthanum, strontium, cobalt, and manganese; x is equal to 0 to 0.7 and
y is equal to 0 to 0.7; the honeycomb ceramics with a metal oxide
coating is to load a metal oxide coating of gamma-Al2O3, CemZr1-mO2,
LaMnAl11O19, BaMnAl11O19 or Sr12Al14O21 on the surface of the honeycomb
ceramics of a dichroite material; wherein, m is equal to 0.1 to 0.8;
the mass ratio of the honeycomb ceramics, the metal oxide coating and
the catalytic activity components is 1.0 : 0.03 to 0.2 : 0.05 to 0.15.
The invention also relates to a preparation method for the catalyst and
the applications of the catalytic combustion thereof to eliminate the
waste gases of volatile organic compound; the dichroite honeycomb
ceramics carrier and the catalytic activity components of the prepared
honeycomb ceramics perovskite catalytic combustion catalyst are
combined by one metal oxide coating with high adhesiveness and thermal
stability, thus leading the catalyst to have the advantages of high
mechanical intensity, high activity and good thermal stability. The
catalyst provided by the invention is simple in preparation method, is
low in the price of the used materials, and has excellent industrial
application prospect. La1-xSrxCoyMn1-yO3 (I).
FINE PARTICLE OF PEROVSKITE
OXIDE, PARTICLE HAVING DEPOSITED PEROVSKITE OXIDE, CATALYST
MATERIAL, CATALYST MATERIAL FOR OXYGEN REDUCTION, CATALYST MATERIAL FOR
FUEL CELL, AND ELECTRODE FOR FUEL CELL
US2009200519
Inventor: SAWAKI YUKO [JP] ; KISHIMOTO MIKIO
Abstract -- A catalyst for
electrodes in solid-polymer fuel cells which comprises metal oxide
particles themselves. It can be used as a substituent for the carbon
particles having platinum deposited thereon and platinum metal
particles which are presently in general use as, e.g., a catalyst for
electrodes in fuel cells, and has a possibility that the amount of
platinum to be used can be greatly reduced as compared with the
conventional carbon particles having platinum deposited thereon, etc.
The catalyst comprises fine transition-metal oxide particles having, in
the main phase, a perovskite structure represented by the general
formula ABO3 (wherein A represents one or more elements selected among
lanthanum, strontium, cerium, calcium, yttrium, erbium, praseodymium,
neodymium, samarium, europium, silicon, magnesium, barium, niobium,
lead, bismuth, and antimony; and B represents one or more elements
selected among iron, cobalt, manganese, copper, titanium, chromium,
nickel, and molybdenum), the fine oxide particles having lattice
constants satisfying the following relationship (1):
<?in-line-formulae description="In-line Formulae"
end="lead"?>1.402<2b/(a+c)<1.422 (1)<?in-line-formulae
description="In-line Formulae" end="tail"?> wherein a and c
represent the minor-axis lengths of the perovskite type crystal lattice
and b represents the major-axis length thereof.
US7291321
PEROVSKITE-BASED CATALYST, ITS
PREPARATION AND ITS USE FOR CONVERSION OF METHANE TO ETHYLENE
Inventor: BAGHERZADEH EBRAHIM
Abstract -- A method of
producing a perovskite catalyst comprising: forming an aqueous slurry
comprising an alkaline earth metal salt, a powdered metal salt and a
powdered transition metal oxide; the aqueous slurry being formed by:
dispersing a powdered alkaline earth metal salt in water, the alkaline
earth metal salt being selected from the group consisting of barium,
calcium and strontium salts adding the powdered metal salt to the
water; and adding the powdered transition metal oxide to the water, the
metal oxide being titanium oxide; and adding a polymeric binder to the
slurry to form a paste; drying the paste for forming a powder; heating
the powder at increasing temperatures at a predetermined profile
commensurate with the polymeric binder; and calcining the heated powder
to form the perovskite catalyst. The catalyst thus formed and the use
thereof for oxidative coupling of methane is also disclosed.
http://www.sciencemag.org/cgi/content/abstract/327/5973/1624?sa_campaign=Email/toc/26-March-2010/10.1126/science.1184087
Strontium-Doped
Perovskites Rival Platinum Catalysts for Treating NOx in Simulated
Diesel Exhaust
Chang Hwan Kim, Gongshin Qi, Kevin Dahlberg, Wei Li*
The high cost and poor thermal durability of current lean nitrogen
oxides (NOx) aftertreatment catalysts are two of the major barriers to
widespread adoption of highly fuel-efficient diesel engines. We
demonstrated the use of strontium-doped perovskite oxides as efficient
platinum substitutes in diesel oxidation (DOC) and lean NOx trap (LNT)
catalysts. The lanthanum-based perovskite catalysts coated on monolith
substrates showed excellent activities for the NO oxidation reaction, a
critical step that demands heavy usage of platinum in a current diesel
aftertreatment system. Under realistic conditions, La1-xSrxCoO3
catalysts achieved higher NO-to-NO2 conversions than a commercial
platinum-based DOC catalyst. Similarly, a La0.9Sr0.1MnO3-based LNT
catalyst achieved NOx reduction performance comparable to that of a
commercial platinum-based counterpart. The results show promise for a
considerably lower-cost diesel exhaust treatment system.
General Motors Global Research and Development, Chemical Sciences and
Materials Systems Lab, 30500 Mound Road, Warren, MI 48090, USA.
* To whom correspondence should be addressed. E-mail: wei.1.li@gm.com
www.greencarcongress.com/2010/03/kim-20100326.html
26 March 2010
GM
R&D Develops and Demonstrates Strontium-Doped Perovskite Catalysts
Rivaling Platinum Catalysts for NOx Control in Diesel Exhaust;
Lower Cost Could Be a Boost for Diesel
Researchers from the General Motors Global Research and Development,
Chemical Sciences and Materials Systems Lab have developed and
demonstrated the use of strontium-doped perovskite oxides as efficient
platinum substitutes in diesel oxidation (DOC) and lean NOx trap (LNT)
catalysts. Their work may help to lower the cost of NOx treatments and
thus ultimately make diesel a more cost-effective automotive fuel. A
paper on the work was published in the 26 March issue of the journal
Science.
One of the obstacles to the more widespread adoption of diesel
engines—especially in the face of increasingly stringent emissions
requirements—is the requirement for a lean NOx aftertreatment system.
The aftertreatment system is a key contributor to the cost premium for
diesel vehicles.
A typical diesel aftertreatment system will include a diesel oxidation
catalyst to oxidizes hydrocarbons, CO, and NO, followed by NOx
reduction. The two leading technologies for NOx reduction in the
oxygen-rich environment are ammonia selective catalytic reduction (SCR)
and a lean NOx trap (LNT).
Many reports have suggested that NO oxidation to NO2
is an important step in lean NOx reduction, because NO2 enhances the
activities of ammonia SCR and LNT. For SCR catalysts, a NO:NO2 ratio of
1:1 is most effective for NOx reduction at lower temperatures (<250
°C). For LNT catalysts, NO must be oxidized to NO2 before
adsorption on the storage components. Because NO2 constitutes less than
10% of NOx in the diesel engine-out exhaust, an oxidation catalyst is
required to increase the NO2 fraction. Platinum has been found to be
especially active for NO oxidation; thus, Pt-based diesel oxidation
(DOC) and LNT catalysts have been widely used for diesel exhaust
aftertreatment. However, they suffer from issues such as high cost and
poor thermal durability. Consequently, there is substantial interest in
the development of better-performing, low-cost, and more durable NO
oxidation catalysts.
—Kim et al.
The catalysts developed by the GM team are based on perovskite oxides,
La1–xSrxCoO3 and La1–xSrxMnO3. Under realistic conditions, La1-xSrxCoO3
catalysts achieved higher NO-to-NO2 conversions than a commercial
platinum-based DOC catalyst. Similarly, a La0.9Sr0.1MnO3-based LNT
catalyst achieved NOx reduction performance comparable to that of a
commercial platinum-based counterpart.
These perovskite catalysts are prone to deactivation by sulfur, a
contaminant present in fuel. However, the oxidation activity of the
catalyst can be improved in the presence of sulfur by adding palladium.
The potential use of perovskites for automotive
applications is hindered by the fact that the perovskites alone are
susceptible to deactivation by S. However, the NOx-treating performance
of Pd/perovskite-based DOC and LNT catalysts in simulated diesel
exhaust demonstrated the potential of Pd/perovskite catalysts as a
viable substitute for Pt in diesel aftertreatment catalysts. This
substitution could drastically reduce the cost of diesel aftertreatment
systems for mobile applications. Lean-burn gasoline engines will also
benefit from this technology.
—Kim et al.
In an accompanying Perspective in Science, James E. Parks, II from Oak
Ridge National Laboratory noted that:
The catalyst developed by Kim et al. greatly reduces
the amount of PGM in LNTs while still maintaining their effectiveness
for NOx reduction from lean engines. This alternative technology will
allow engineers greater flexibility as they work to develop better
catalysts in a market where volatile PGM prices have made commercial
introduction of fuel-efficient lean vehicles challenging. It is
possible that these catalysts may allow lean-burn technology to be used
with minimal added cost compared to conventional engines.
Resources
Chang Hwan Kim, Gongshin Qi, Kevin Dahlberg, Wei Li (2010)
Strontium-Doped Perovskites Rival Platinum Catalysts for Treating NOx
in Simulated Diesel Exhaust. Science Vol. 327. no. 5973, pp. 1624 -
1627 doi: 10.1126/science.1184087
James E. Parks, II (2010) Less Costly Catalysts for Controlling Engine
Emissions. Science Vol. 327. no. 5973, pp. 1584 - 1585 doi:
10.1126/science.1187154
http://bioage.typepad.com/.a/6a00d8341c4fbe53ef0133ec3a7d49970b-popup
NOx conversion profiles. Commercial LNT (black dashed line);
La0.9Sr0.1MnO3-based LNT (green line); La0.9Sr0.1MnO3-based LNT after a
S loading of 1 g liter–1 catalyst (red line); and La0.9Sr0.1MnO3-based
LNT after desulfation (blue line) as a function of temperature. Credit:
Kim et al.
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