This document discusses vehicle emissions and methods for controlling them. It begins by describing the main pollutants from vehicle emissions like hydrocarbons, carbon monoxide, nitrogen oxides, and particulate matter. It then discusses emission standards in countries like India and the US. The rest of the document details how catalytic converters work to reduce emissions by converting pollutants into less harmful substances through catalyzed chemical reactions. It also discusses emissions of greenhouse gases and technologies being developed to meet emission standards.
(COD) ̄Young Call Girls In Dwarka , New Delhi꧁❤ 7042364481❤꧂ Escorts Service i...
Pollucare slideshow upload
1. CONTROLLING AUTOMOBILE POLLUTION IN A UNIQUE WAY
CONTROLLING AUTOMOBILE POLLUTION IN A UNIQUE WAY
POLLUCARE
AUTO EMISSION IMPROVER
IMPROOVING AUTOMOBILE EMISSIONS (BIO SOLUTION)
Introduction
Vehicle emissions control is the study and practice of reducing the motor vehicle emissions --
emissions produced by motor vehicles, especially internal combustion engines.
2. Emissions of many air pollutants have been shown to have variety of negative effects on public
health and the natural environment. Emissions that are principal pollutants of concern include:
* Hydrocarbons - A class of burned or partially burned fuel, hydrocarbons are toxins.
Hydrocarbons are a major contributor to smog, which can be a major problem in urban areas.
Prolonged exposure to hydrocarbons contributes to asthma, liver disease, , lung disease, and
cancer. Regulations governing hydrocarbons vary according to type of engine and jurisdiction;
in some cases, "non-methane hydrocarbons" are regulated, while in other cases, "total
hydrocarbons" are regulated. Technology for one application (to meet a non-methane
hydrocarbon standard) may not be suitable for use in an application that has to meet a total
hydrocarbon standard. Methane is not directly toxic, but is more difficult to break down in a
catalytic converter, so in effect a "non-methane hydrocarbon" regulation can be considered
easier to meet. Since methane is a greenhouse gas, interest is rising in how to eliminate
emissions of it.
* Carbon monoxide (CO) - A product of incomplete combustion, carbon monoxide reduces
the blood's ability to carry oxygen; overexposure (carbon monoxide poisoning) may be fatal.
Carbon Monoxide poisoning is a major killer.
* Nitrogen oxides (NOx) - Generated when nitrogen in the air reacts with oxygen at the high
temperature and pressure inside the engine. NOx is a precursor to smog and acid rain. NOx is a
mixture of NO, N2O, and NO2. NO2 is extremely reactive. It destroys resistance to respiratory
infection. NOx production is increased when an engine runs at its most efficient (i.e. hottest) part
of the cycle.
NOx, a major air pollutant causes asthma and respiratory and heart diseases.
* Particulate matter – Soot or smoke made up of particles in the micrometre size range:
Particulate matter causes negative health effects, including but not limited to respiratory disease
and cancer.
* Sulfur oxide (SOx) - A general term for oxides of sulfur, which are emitted from motor
vehicles burning fuel containing sulfur. Reducing the level of fuel sulfur reduces the level of
Sulfur oxide emitted from the tailpipe. Refineries generally fight requirements to do this because
of the increased costs to them, ignoring the increased costs to society as a whole.
* Volatile organic compounds (VOCs) - Organic compounds which typically have a boiling
point less than or equal to 250 °C; for example chlorofluorocarbons (CFCs) and formaldehyde.
Volatile organic compounds are a subsection of Hydrocarbons that are mentioned separately
because of their dangers to public health.
The impact of internal combustion engines on the environment and our lifestyles has been
considerable.
There is a tremendous increase in the Number, Power, Speed and Size of the Vehicles.
Several of the compounds present in diesel and gasoline engine exhausts are known to be
carcinogenic and/or mutagenic .
3. It is high time to concentrate on simpler control methods on exhaust emissions so as to
reduce the impact of these emissions on health and the environment.
How stringent are emission regulation acts
Indian Emission Standards (4-Wheel Vehicles)
Standard Reference Date Region
India 2000 Euro 1 2000 Nationwide
Bharat Stage II Euro 2 2001 NCR*, Mumbai, Kolkata, Chennai
2003.04 NCR*, 12 Cities†
2005.04 Nationwide
Bharat Stage III Euro 3 2005.04 NCR*, 12 Cities† 2010.04 Nationwide
Bharat Stage IV Euro 4 2010.04 NCR*, 12 Cities†
* National Capital Region (Delhi)
† Mumbai, Kolkata, Chennai, Bengaluru, Hyderabad, Ahmedabad, Pune, Surat, Kanpur, Lucknow,
Sholapur, and Agra
Emission Standards for Light-Duty Diesel Vehicles, g/km
Year Reference CO HC HC+NOx PM
1992 - 17.3-32.6 2.7-3.7 - -
1996 - 5.0-9.0 - 2.0-4.0 -
2000 Euro 1 2.72-6.90 - 0.97-1.70 0.14-0.25
2005† Euro 2 1.0-1.5 - 0.7-1.2 0.08-0.
4. The California Air Resources Board proposed a new regulation to control emissions of
greenhouse gases (GHG) from light-duty vehicles, which calls for a 30% GHG emission
reduction phased-in from 2009 to 2014. The proposal has been developed under the California
bill AB 1493, adopted in 2002, which requires the ARB to develop and adopt, by January 1,
2005, regulations that achieve the ―maximum feasible reduction of greenhouse gases emitted
by passenger vehicles and light-duty trucks‖. It is the first legislation in US history to regulate
carbon dioxide and other greenhouse gas emissions from cars and light-duty trucks.
The proposal covers vehicle climate change emissions comprised of four main components: (1)
carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O, not to be confused with the
regulated NOx emissions, which include NO and NO2) emissions resulting directly from
operation of the vehicle, (2) CO2 emissions resulting from operating the air conditioning system
(indirect AC emissions), (3) refrigerant emissions from the air conditioning system due to either
leakage, losses during recharging, or release from scrappage of the vehicle at end of life (direct
AC emissions), and (4) upstream emissions associated with the production of the fuel used by
the vehicle.
The climate change emission standard proposal introduces CO2-equivalent emission standards
(where the other GHG emissions are converted to CO2 based on their climate warming
potential), which are incorporated into the current California LEV program. Accordingly, there
5. would be a CO2 equivalent fleet average emission requirement for the passenger car/light-duty
truck 1 (PC/LDT1) category and another for the light-duty truck 2 (LDT2) category, just as there
are fleet average emission requirements for criteria pollutants for both these categories.
The ARB considers the following groups of technologies for meeting of the CO2 emission
standards:
1. Engine, Drivetrain, and Other Vehicle Modifications—valvetrain, transmission, vehicle
accessory, hybrid-electric, and overall vehicle modifications designed to reduce engine exhaust
CO2 emissions from conventional vehicles
2. Mobile Air-Conditioning System—air conditioning unit modifications to reduce vehicle CO2
emissions and refrigerant modifications to reduce emissions of HFC refrigerants, such as HFC-
134a
3. Alternative Fuel Vehicles—the use of vehicles that use fuels other than gasoline and diesel to
reduce the sum of exhaust emissions and ―upstream‖ fuel delivery emissions of climate change
gases
4. Exhaust Catalyst Improvement—exhaust aftertreatment alternatives to reduce tailpipe emissions
of CH4 and N2O (the latter gas being a common by-product generated in three-way catalytic
converters)
5. High speed direct injection diesel engines are named as a technology that can provide
significant CO2 reductions when compared to conventional gasoline engines. Other engine and
drivertrain technologies analyzed by the ARB include valvetrain and charge modifications,
variable compression ratio, gasoline direct injection, homogeneous charge compression ignition,
and more.
6. The regulation is expected to be challenged in court by the automotive industry and, possibly, by
the federal government. The manufacturers will likely argue that CO2 emission regulation is in
fact a disguised form of more stringent fuel economy standards, which are outside California
jurisdiction. On the other hand, the California move will trigger similar actions by other states,
many of which are disappointed with the indifference about climate change by the federal
government.
Source: California ARB
6. A mobile emission reduction credit (MERC) is an emission reduction credit generated within the
transportation sector. The term ―mobile sources‖ refers to motor vehicles, engines, and
equipment that move, or can be moved, from place to place.[1] Mobile sources include vehicles
that operate on roads and highways ("on-road" or "highway" vehicles), as well as nonroad
vehicles, engines, and equipment. Examples of mobile sources are passenger cars, light trucks,
large trucks, buses, motorcycles, earth-moving equipment, nonroad recreational vehicles (such
as dirt bikes and snowmobiles), farm and construction equipment, cranes, lawn and garden
power tools, marine engines, ships, railroad locomotives, and airplanes. In California, mobile
sources account for about 60 percent of all ozone forming emissions and for over 90 percent of
all carbon monoxide (CO) emissions from all sources.
11. A catalytic converter (colloquially, "cat" or "catcon") is a device used to convert toxic exhaust
emissions from an internal combustion engine into non-toxic substances. Inside a catalytic
converter, a catalyst stimulates a chemical reaction in which noxious byproducts of combustion
are converted to less toxic substances by dint of catalysed chemical reactions. The specific
reactions vary with the type of catalyst installed. Most present-day vehicles that run on gasoline
are fitted with a "three way" converter, so named because it converts the three main pollutants
in automobile exhaust: an oxidising reaction converts carbon monoxide(CO) and unburned
hydrocarbons(HC), and a reduction reaction converts oxides of nitrogen (NOx) to produce
carbon dioxide(CO2), nitrogen(N2), and water(H2O).
The first widespread introduction of catalytic converters was in the United States market, where
1975 model year automobiles were so equipped to comply with tightening U.S. Environmental
Protection Agency regulations on automobile exhaust emissions. The catalytic converters fitted
were two-way models, combining carbon monoxide(CO) and unburned hydrocarbons(HC) to
produce carbon dioxide(CO2) and water(H2O). Two-way catalytic converters of this type are
now considered obsolete except on lean burn engines.[citation needed] Since most vehicles at
the time used carburetors that provided a relatively rich air-fuel ratio, oxygen (O2) levels in the
exhaust stream were in general insufficient for the catalytic reaction to occur. Therefore, most
such engines were also equipped with secondary air injection systems to induct air into the
exhaust stream to allow the catalyst to function.
Catalytic converters are still most commonly used on automobile exhaust systems, but are also
used on generator sets, forklifts, mining equipment, trucks, buses, locomotives, airplanes and
other engine fitted devices. This is usually in response to government regulation, either through
direct environmental regulation or through Health and Safety regulations.
The catalytic converter consists of several components:
1. The catalyst core, or substrate. For automotive catalytic converters, the core is usually a ceramic
monolith with a honeycomb structure. Metallic foil monoliths made of FeCrAl are used in some
applications. This is partially a cost issue. Ceramic cores are inexpensive when manufactured in
large quantities. Metallic cores are less expensive to build in small production runs. Either
material is designed to provide a high surface area to support the catalyst washcoat, and
therefore is often called a "catalyst support". The cordierite ceramic substrate used in most
12. catalytic converters was invented by Rodney Bagley, Irwin Lachman and Ronald Lewis at
Corning Glass, for which they were inducted into the National Inventors Hall of Fame in 2002.
2. The washcoat. A washcoat is a carrier for the catalytic materials and is used to disperse the
materials over a high surface area. Aluminum oxide, Titanium dioxide, Silicon dioxide, or a
mixture of silica and alumina can be used. The catalytic materials are suspended in the
washcoat prior to applying to the core. Washcoat materials are selected to form a rough,
irregular surface, which greatly increases the surface area compared to the smooth surface of
the bare substrate. This maximizes the catalytically active surface available to react with the
engine exhaust.
3. The catalyst itself is most often a precious metal. Platinum is the most active catalyst and is
widely used, but is not suitable for all applications because of unwanted additional
reactions[vague] and high cost. Palladium and rhodium are two other precious metals used.
Rhodium is used as a reduction catalyst, palladium is used as an oxidation catalysts, and
platinum is used both for reduction and oxidation. Cerium, iron, manganese and nickel are also
used, although each has its own limitations. Nickel is not legal for use in the European Union
(because of its reaction with carbon monoxide into nickel tetracarbonyl). Copper can be used
everywhere except North America, where its use is illegal because of the formation of dioxin.
For compression-ignition (i.e., diesel engines), the most-commonly-used catalytic converter is
the Diesel Oxidation Catalyst (DOC). This catalyst uses O2 (oxygen) in the exhaust gas stream
to convert CO (carbon monoxide) to CO2 (carbon dioxide) and HC (hydrocarbons) to H2O
(water) and CO2. These converters often operate at 90 percent efficiency, virtually eliminating
diesel odor and helping to reduce visible particulates (soot). These catalyst are not active for
NOx reduction because any reductant present would react first with the high concentration of
O2 in diesel exhaust gas.
Reduction in NOx emissions from compression-ignition engine has previously been addressed
by the addition of exhaust gas to incoming air charge, known as exhaust gas recirculation
(EGR). In 2010, most light-duty diesel manufactures in the U.S. added catalytic systems to their
vehicles to meet new federal emissions requirements. There are two techniques that have been
13. developed for the catalytic reduction of NOx emissions under lean exhaust condition - selective
catalytic reduction (SCR) and the lean NOx trap or NOx adsorber. Instead of precious metal-
containing NOx adsorbers, most manufacturers selected base-metal SCR systems that use a
reagent such as ammonia to reduce the NOx into nitrogen. Ammonia is supplied to the catalyst
system by the injection of urea into the exhaust, which then undergoes thermal decomposition
and hydrolysis into ammonia. One trademark product of urea solution, also referred to as Diesel
Emission Fluid (DEF), is AdBlue.
Diesel exhaust contains relatively high levels of particulate matter (soot), consisting in large part
of elemental carbon. Catalytic converters cannot clean up elemental carbon, though they do
remove up to 90 percent of the soluble organic fraction, so particulates are cleaned up by a soot
trap or diesel particulate filter (DPF). A DPF consists of a Cordierite or Silicon Carbide substrate
with a geometry that forces the exhaust flow through the substrate walls, leaving behind trapped
soot particles. As the amount of soot trapped on the DPF increases, so does the back pressure
in the exhaust system. Periodic regenerations (high temperature excursions) are required to
initiate combustion of the trapped soot and thereby reducing the exhaust back pressure. The
amount of soot loaded on the DPF prior to regeneration may also be limited to prevent extreme
exotherms from damaging the trap during regeneration. In the U.S., all on-road light, medium
and heavy-duty vehicles powered by diesel and built after January 1, 2007, must meet diesel
particulate emission limits that means they effectively have to be equipped with a 2-Way
catalytic converter and a diesel particulate filter. Note that this applies only to the diesel engine
used in the vehicle. As long as the engine was manufactured before January 1, 2007, the
vehicle is not required to have the DPF system. This led to an inventory runup by engine
manufacturers in late 2006 so they could continue selling pre-DPF vehicles well into 2007.
Most of the pollution put out by a car occurs during the first five minutes before the catalytic
converter has warmed up sufficiently.
In 1999, BMW introduced the Electric Catalytic Convert, or "E-CAT", in their flagship E38 750iL
sedan. Coils inside the catalytic converter assemblies are heated electrically just after engine
start, bringing the catalyst up to operating temperature much faster than traditional catalytic
converters can, providing cleaner cold starts and low emission vehicle (LEV) compliance.
15. purpose of the positive crankcase ventilation (PCV) system, is to take the vapors produced in
the crankcase during the normal combustion process, and redirecting them into the air/fuel
intake system to be burned during combustion. These vapors dilute the air/fuel mixture so they
have to be carefully controlled and metered in order to not affect the performance of the engine.
This is the job of the positive crankcase ventilation (PCV) valve. At idle, when the air/fuel
mixture is very critical, just a little of the vapors are allowed in to the intake system. At high
speed when the mixture is less critical and the pressures in the engine are greater, more of the
vapors are allowed in to the intake system. When the valve or the system is clogged, vapors will
back up into the air filter housing or at worst, the excess pressure will push past seals and
create engine oil leaks. If the wrong valve is used or the system has air leaks, the engine will
idle rough, or at worst, engine oil will be sucked out of the engine.
The purpose of the exhaust gas recirculation valve (EGR) valve is to meter a small amount of
exhaust gas into the intake system, this dilutes the air/fuel mixture so as to lower the
combustion chamber temperature. Excessive combustion chamber temperature creates oxides
of nitrogen, which is a major pollutant. While the EGR valve is the most effective method of
controlling oxides of nitrogen, in it's very design it adversely affects engine performance. The
engine was not designed to run on exhaust gas. For this reason the amount of exhaust entering
the intake system has to be carefully monitored and controlled. This is accomplished through a
16. series of electrical and vacuum switches and the vehicle computer. Since EGR action reduces
performance by diluting the air /fuel mixture, the system does not allow EGR action when the
engine is cold or when the engine needs full power.
EVAPORATIVE CONTROLS
Gasoline evaporates quite easily. In the past, these evaporative emissions were vented into the
atmosphere. 20% of all HC emissions from the automobile are from the gas tank. In 1970
legislation was passed, prohibiting venting of gas tank fumes into the atmosphere. An
evaporative control system was developed to eliminate this source of pollution. The function of
the fuel evaporative control system is to trap and store evaporative emissions from the gas tank
and carburetor. A charcoal canister is used to trap the fuel vapors. The fuel vapors adhere to
the charcoal, until the engine is started, and engine vacuum can be used to draw the vapors into
the engine, so that they can be burned along with the fuel/air mixture. This system requires the
use of a sealed gas tank filler cap. This cap is so important to the operation of the system, that a
test of the cap is now being integrated into many state emission inspection programs. Pre-1970
cars released fuel vapors into the atmosphere through the use of a vented gas cap. Today with
the use of sealed caps, redesigned gas tanks are used. The tank has to have the space for the
vapors to collect so that they can then be vented to the charcoal canister. A purge valve is used
to control the vapor flow into the engine. The purge valve is operated by engine vacuum. One
common problem with this system is that the purge valve goes bad and engine vacuum draws
fuel directly into the intake system. This enriches the fuel mixture and will foul the spark plugs.
Most charcoal canisters have a filter that should be replaced periodically. This system should be
checked when fuel mileage drops.
Lead
Splashing and/or washing plant shoots with aqueous solutions of the chelates Ca EDTA (max.
0·5%) or Na-polyphosphate (max. 0·5%) is an effective way to reduce contamination and uptake
of lead by plants in areas where emission of airborne lead occurs. If the decomposition of
chelates in the rhizosphere is prevented, they are also effective in reducing lead uptake by the
plant roots.
(K. Isermann; A method to reduce contamination and uptake of lead by plants from car exhaust
gases; Environmental Pollution (1970); Volume 12, Issue 3, March 1977, Pages 199-203)
Catalysts
Metal-enriched zeolites are known to effectively catalyze nitrous oxide in automobile exhaust.
Most of these catalysts, however, break down in the presence of water, which can compose 5%
to 10% of the exhaust gas. A reproducible method for producing iron-rich ZSM-5 zeolites that do
not break down in the presence of
water was developed.
Rubrivivax gelatinosus (Syn: Methylibium petroleiphilum)
Upon feeding CO to the gas phase of a photosynthetic bacterium Rubrivivax gelatinosus CBS, a
CO oxidation: H2 production pathway is quickly induced. Hydrogen is produced according to the
equation CO + H2O → CO2 + H2. Two enzymes are known to be involved in this pathway: a CO
dehydrogenase (CODH) with a pH optimum of 8.0 and above, and a hydrogenase with a pH
optimum near 7.5. Carbon monoxide dehydrogenase also displays a temperature optimum near
50°C. When CO mass transfer is not limited during a CO uptake measurement, an extreme fast
rate of CO uptake was determined, allowing for the removal of near 87% of the dissolved CO
from a bacterial suspension within 10 s. This process has therefore two potential applications,
17. one in the production of H2 gas as a clean renewable fuel using the linked CO oxidation: H2
production pathway, and another in using the CODH enzyme itself as a fuel-gas conditioning
catalyst. These applications thereby will improve the overall H2 economy when gasified waste
biomass serves as the inexpensive feedstock.
Treatment of the exhaust to improve tailpipe emissions
1. By using beneficial microbes which will consume/ degrade the Benzene, CO2, CO, HC,
CH4, N2O, NO, NO2, Toluene etc.
2. By using natural Gas Adsorbants which bind the emissions
3. By using Oxygen Liberators which improve Oxygen.
4. By Using 32.5% Nitrogen solution which can remove enough NOx from auto exhaust to
comply with even stringent statutory limits
Pollucare cleans the exhaust after combustion. A portion of the Pollucare is held in a
separate storage tank and injected as a fine mist into the hot exhaust gases. The heat
breaks the Nitrogen solution down into ammonia—the actual NOx-reducing agent.
Through a catalytic converter, the ammonia breaks the NOx down to harmless nitrogen
18. (N) gas and water vapor. The exhaust is no longer a pollutant; the atmosphere is about
80% nitrogen gas.
Also the Oxygen liberators provide oxygen which is essential for the microbes and the
oxygen left over after the consumption by the microbes comes with the final out flow of
the treated emissions
The Gas adsorbants bind the obnoxious gases.
The microbes degrade CO2 and CO into Carbon and Oxygen. A part of the Carbon is
consumed by them. They also breakother pollutants.
References
1. Alsberg T, ed. Fuel impact on exhaust emissions from vehicles (in Swedish). Statens Naturvårdsverk, SNV PM 3680. Solna,
Sweden:National Swedish Environmental Protection Board, 1989.
2. Alsberg T, Stenberg U, Westerholm R, Strandell M, Rannug U, Sundvall A, Romert L, Bernson V, Petterson B, Toftgård R,
Franzen B, Jansson M, Gustafsson J-Å, Egebäck K-E, Tejle G. Chemical and biological characterization of organic material from
gasoline exhaust particles. Environ Sci Technol 19:43-50 (1985).
3. Alsberg T, Strandell M, Westerholm R, Stenberg U. Fractionation and chemical analysis of gasoline exhaust particulate extract
in connection with biological testing. Environ Int Vol 11:249-257 (1985).
4. Alsberg T, Westerholm R, Stenberg U, Strandell M, Jansson B. Particle associated organic halides in exhausts from gasoline
and diesel fueled vehicles. In: The Eight International Symposium on Mechanisms, Methods, and Metabolism (Cooke M, Dennis
A, eds). Columbus, OH:Batelle Press, 1983;87-97.
5. Applied and Environmental Microbiology, December 2003, p. 7257-7265, Vol. 69, No. 12
0099-2240/03/$08.00+0 DOI: 10.1128/AEM.69.12.7257-7265.2003
6. Assih, E. A., A. S. Ouattara, S. Thierry, J.-L. Cayhol, M. Labat, and H. Macarie. 2002. Stenotrophomonas acidaminiphila sp.
nov., a strictly aerobic bacterium isolated from an upflow anaerobic sludge blanket (UASB) reactor. Int. J. Syst. Evol. Microbiol.
52:559-568.[Abstract/Free Full Text]
7. Auling, G., J. Busse, M. Han, H. Hennecke, R. Kroppenstedt, A. Probst, and E. Stackenbrandt. 1988. Phylogenetic
heterogeneity and chemotaxonomic properties of certain gram-negative aerobic carboxydobacteria. Syst. Appl. Microbiol.
10:264-272.
8. Bartholomew, G. W., and M. Alexander. 1982. Microorganisms responsible for the oxidation of carbon monoxide in soil.
Environ. Sci. Technol. 16:300-301.
9. Bayona J, Markides K, Lee M. Characterization of polar polycyclic aromatic compounds in a heavy-duty diesel exhaust
particulate by capillary column gas chromatography and high resulation mass spectrometry. Environ Sci Technol 22:1440-1447
(1988).
10. Bertilsson B-I, Gustavsson L. Experiences of heavy-duty alcohol fueled diesel ignition engines. SAE Paper No. 871672.
Warrendale, PA:Society of Automotive Engineers, 1987.
11. Björkman E, Egebäck K-E. Ethanol as a motor fuel (in Swedish). Statens Naturvårdsverk, SNV Report No. 3304. Studsvik,
Sweden:National Swedish Environmental Protection Board, 1987.
12. Boettcher, K. J., B. J. Barber, and J. T. Singer. 2001. Additional evidence that juvenile oyster disease is caused by a member
of the Roseobacter group, and colonization of non-infected animals by Stappia stellulata-like strains. Appl. Environ. Microbiol.
66:3924-3930.[CrossRef]
13. Cartillieri WP, Wachter WF. Status report on a primary surway of strategies to meet US-91 HD diesel emission standards without
exhaust gas after treatment. SAE Paper No. 870342. Warrendale, PA:Society of Automotive Engineers, 1987.
14. Chung, W.-K., and G. M. King. 2001. Isolation, characterization and polyaromatic hydrocarbon degradation potential of aerobic
bacteria from marine macrofaunal burrow sediments and description of Lutibacterium anuloederans gen. nov., sp. nov., and
Cycloclasticus spirillensus sp. nov. Appl. Environ. Microbiol. 67:5585-5592.[Abstract/Free Full Text]
19. 15. Coenye, T., S. Laevens, A. Willems, M. Ohlen, W. Hannant, J. R. W. Govan, M. Gillis, E. Falsen, and P. Vandamme.2001 .
Burkholderia fungorum sp. nov. and Burkholderia caledonica sp. nov., two new species isolated from the environment, animals
and human clinical samples. Int. J. Syst. Evol. Microbiol. 51:1099-1107.[Abstract]
16. Conrad, R. 1996. Soil microorganisms as controllers of atmospheric trace gases (H2, CO, CH4, OCS, N2O, and NO). Microbiol.
Rev. 60:609-640.[Medline]
17. Conrad, R., and W. Seiler. 1980. Role of microorganisms in the consumption and production of atmospheric carbon monoxide
by soil.Appl. Environ. Microbiol. 40:437-445.
18. Conrad, R., and W. Seiler. 1982. Utilization of traces of carbon monoxide by aerobic oligotrophic microorganisms in ocean, lake
and soil. Arch. Microbiol. 132:41-46.
19. Conrad, R., O. Meyer, and W. Seiler. 1981. Role of carboxydobacteria in consumption of atmospheric carbon monoxide by soil.
Appl. Environ. Microbiol. 42:211-215.
20. Crutzen, P. J., and L. T. Gidel. 1983. A two-dimensional photochemical model of the atmosphere. 2: The tropospheric budgets
of the anthropogenic chlorocarbons, CO, CH4, CH3Cl and the effect of various NOx sources on tropospheric ozone. J. Geophys.
Res. 88:6641-6661.
21. Daniel, J. S., and S. Solomon. 1998. On the climate forcing of carbon monoxide. J. Geophys. Res. 103:13249-13260.
22. de Lajudie, P., A. Willems, G. Nick, F. Moreira, F. Molouba, B. Hoste, U. Torck, M. Neyra, M. D. Collins, K. Lindström, B.
Dreyfus, and M. Gillis. 1998. Characterization of tropical tree rhizobia and description of Mesorhizobium plurifarium sp. nov. Int.
J. Syst. E vol. Microbiol. 48:369-382.[Abstract/Free Full Text]
23. Diesel particulate control, trap, and filtration systems. SAE Paper No. SP 896. Warrendale, PA:Society of Automotive Engineers,
1992.
24. Egebäck K-E, Bertilsson B-M. Chemical and biological characterization of exhaust emissions from vehicles fueled with gasoline,
alcohol, LPG, and diesel. Statens Naturvårdsverk, SNV PM 1635. Stockholm:National Swedish Environmental Protection Board,
1983.
25. Egebäck K-E, Hedbom A. Report No. 3840 (in Swedish). Stockholm:Swedish Environmental Protection Agency, 1990.
26. Egebäck K-E, Hedbom A. Report No. 9052 (in Swedish). Stockholm:Swedish Motor Vehicle Inspection Company, 1990.
27. Egebäck K-E, Tejle G, Laveskog A. Investigation of regulated and unregulated pollutants from different fuel/engine concerts and
temperatures (in Swedish). Statens Naturvårdsverk, SNV Report No. 1812. Studsvik,Sweden:National Swedish Environmental
Protection Board, 1984.
28. Egebäck K-E, Tejle G. SNV PM 1675 (in Swedish). Studsvik, Sweden:Motor Vehicle Emission Laboratory, 1983.
29. Egebäck K-E, Westerholm R. Regulated and unregulated pollutants from vehicles fueled with alcohols. In: Proceedings of the
Eighth International Symposium on Alcohol Fuels, 13-16 November 1988, Tokyo, Japan, 1988;431-436.
30. Egebäck K-E. Technical Report No. PM Bil-75 (in Swedish). Studsvik, Sweden:Motor Vehicle Emission Laboratory, 1975.
31. Egebäck K-E. Velocity, pollution emissions, gasoline fueled vehicles (in Swedish). Statens Naturvårdsverk, SNV Report No.
3276. Studsvik, Sweden:National Swedish Environmental Protection Board, 1987.
32. Grägg K, Egebäck K-E. Emission measurements on an ethanol fueled bus (in Swedish). Statens Naturvårdsverk, Report No.
871007. Studsvik, Sweden:National Swedish Environmental Protection Board, 1987.
33. Haglund P, Alsberg T, Bergman Å, Jansson B. Analysis of halogenated polycyclic aromatic hydrocarbons in urban air, snow, and
automobile exhaust. Chemosphere 16:2441-2450 (1987).
34. Haglund P, Egebäck K-E, Jansson B. Analysis polybrominated dioxins and furans in vehicle exhaust. Chemosphere 17:2129-
2140 (1988).
35. Hardy, K., and G. M. King. 2001. Enrichment of a high-affinity CO oxidizer in Maine forest soil. Appl. Environ. Microbiol.
67:3671-3676.[Abstract/Free Full Text]
36. Holmberg B, Ahlborg U, eds. Mutagenicity and carcinogenicity of air pollutants. Environ Health Perspect 47:1-30 (1983).
37. IARC. Diesel and Gasoline Engine Exhausts and Some Nitroarenes. In: IARC Monographs on the Evaluation of the
Carcinogenic Risks to Humans, Vol 46. Lyon:International Agency for Research on Cancer, 1989.
38. IARC. Polynuclear Aromatic Compounds, Part 1, Chemical, Environmental and Experimental Data. In: IARC Monographs on the
Evaluation of the Carcinogenic Risk of Chemicals to Humans, Vol 32. Lyon:International Agency for Research on Cancer, 1983.
39. IMechE. The vehicle and the environment. In: XXIV FISITA Congress 7-11 June 1992, the Council of the Institution of
Mechanical Engineers. London:IMechE, 1992;1-153.
40. IMechE. Vehicle emissions and their impact on European air quality. In: Proceedings of the Institution of Mechanical Engineers
International Conference, 3-5 November 1987, Institution of Mechanical Engineers. London:IMechE, 1987;1-372.
20. 41. Johnson, J. E., and T. S. Bates. 1996. Sources and sinks of carbon monoxide in the mixed layer of the tropical South Pacific
Ocean. Global Biogeochem. Cycles 10:347-359.
42. Jones, R. D. 1991. Carbon monoxide and methane distribution and consumption in the photic zone of the Sargasso Sea.Deep-
Sea Res. 38:625-635.
43. Jones, R. D., and R. Y. Morita. 1983. Carbon monoxide oxidation by chemolithotrophic ammonium oxidizers.Can. J. Microbiol.
29:1545-1551.
44. Jones, R. D., R. Y. Morita, and R. P. Griffiths. 1984. Method for estimating chemolithotrophic ammonium oxidation using
carbon monoxide. Mar. Ecol. Prog. Ser. 17:259-269.
45. Kang, B. S., and Y. M. Kim. 1999. Cloning and molecular characterization of the genes for carbon monoxide dehydrogenase
and localization of molybdopterin, flavin adenine dinucleotide, and iron-sulfur centers in the enzyme of Hydrogenophaga
pseudoflava. J. Bacteriol. 181:5581-5590.[Abstract/Free Full Text]
46. Khalil, M. A. K. 1999. Atmospheric carbon monoxide. Chemosphere: Global Change Sci. 1:ix.
47. King, G. M. 1999. Attributes of atmospheric carbon monoxide oxidation by Maine forest soils. Appl. Environ. Microbiol. 65:5257-
5264.[Abstract/Free Full Text]
48. King, G. M. 1999. Characteristics and significance of atmospheric carbon monoxide consumption by soils.Chemosphere: Global
Change Sci. 1:53-63.[CrossRef]
49. King, G. M. 2000. Impacts of land use on atmospheric carbon monoxide consumption by soils. Global Biogeochem. Cycles
14:1161-1172.
50. King, G. M. 2001. Aspects of carbon monoxide production and consumption by marine macroalgae. Mar. Ecol. Prog. Ser.
224:69-75.
51. King, G. M. 2003. Contributions of atmospheric CO and hydrogen uptake to microbial dynamics on recent Hawaiian volcanic
deposits. Appl. Environ. Microbiol. 69:4067-4075.[Abstract/Free Full Text]
52. King, G. M., and M. Hungria. 2002. Soil-atmosphere CO exchanges and microbial biogeochemistry of CO transformations in a
Brazilian agricultural ecosystem. Appl. Environ. Microbiol. 68:4480-4485.[Abstract/Free Full Text]
53. King, G. M.Uptake of carbon monoxide and hydrogen at environmentally relevant concentrations by mycobacteria. Appl.
Environ. Microbiol., in press.
54. Lane, D. J. 1991. 16S/23S rRNA sequencing, p.115 -175. In E. Stackebrandt and M. Goodfellow (ed.), Nucleic acid techniques
in bacterial systematics. John Wiley & Sons, New York, N.Y.
55. Lorite, M. J., J. Tachil, J. Sanjuan, O. Meyer, and E. J. Bedmar. 2000. Carbon monoxide dehydrogenase activity in
Bradyrhizobium japonicum. Appl. Environ. Microbiol. 66:1871-1876.[Abstract/Free Full Text]
56. Marklund S, Rappe C, Tysklind M, Egebäck K-E. Identification of polyclorinated dibenzofurans and dioxins in exhaust from cars
run on leaded gasoline. Chemosphere 16:29-36 (1987).
57. Marklund S. Dioxin emissions and environmental imissions. A study of polychlorinated dibenzodioxins and dibenzofurans in
combustion process. Ph.D. Thesis. University of Umeå, Umeå, Sweden, 1990.
58. Meyer, O., K. Frunzke, D. Gadkari, S. Jacobitz, I. Hugendieck, and M. Kraut. 1990. Utilization of carbon monoxide by
aerobes: recent advances. FEMS Microbiol. Rev. 87:253-260.[CrossRef]
59. Moghissi A, ed. Genotoxic air pollutants. Environ Internat 11:103-418 (1985).
60. Morsdorf, G., K. Frunzke, D. Gadkari, and O. Meyer. 1992. Microbial growth on carbon monoxide. Biodegradation 3:61-82.
61. Moulin, L., A. Munive, B. Dreyfus, and C. Boivin-Masson. 2001. Nodulation of legumes by members of the beta-subclass of
Proteobacteria. Nature 411:948-950.[CrossRef][Medline]
62. Park, S. W., E. H. Hwang, H. Park, J. A. Kim, J. Heo, K. H. Lee, T. Song, E. Kim, Y. T. Ro, S. W. Kim, and Y. M. Kim.2003 .
Growth of mycobacteria on carbon monoxide and methanol. J. Bacteriol. 185:142-147.[Abstract/Free Full Text]
63. Prather, M. J., R. Derwent, D. Ehhalt, P. Fraser, E. Sanhueza, and X. Zhou. 1995. Other trace gases and atmospheric
chemistry, p. 73-126. In J. T. Houghton, L. G. Meira Filho, J. Bruce, H. Lee, B. A. Callender, E. Haites, N. Harris, and K. Maskell
(ed.), Climate change 1994. Cambridge University Press, Cambridge, United Kingdom.
64. Rainey, F. A., and J. Wiegel. 1996. 16S ribosomal DNA sequence analysis confirms the close relationship between the general
Xanthobacter, Azorhizobium, and Aquabacter and reveals a lack of phylogenetic coherence among Xanthobacter species. Int. J.
Syst. Bacteriol. 46:607-610.
65. Rannug U, Sundvall A. Mutagenic properties of gasoline exhaust. Environ Int 11:303-309 (1985).
66. Rich, J. J., and G. M. King. 1998. Carbon monoxide oxidation by bacteria associated with the roots of freshwater macrophytes.
Appl. Environ. Microbiol. 64:4939-4943.[Abstract/Free Full Text]
21. 67. Rüger, H.-J., and M. G. Höfle. 1992. Marine star-shaped-aggregate-forming bacteria: Agrobacterium atlanticum sp. nov.;
Agrobacterium meteori sp. nov.; Agrobacterium ferrugineum sp. nov., nom. rev.; Agrobacterium gelatinovorum sp. nov., nom.
rev.; and Agrobacterium stellulatum sp. nov., nom. rev. Int. J. Syst. Bacteriol. 42:133-143.[Abstract]
68. Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor
Laboratory Press, Cold Spring Harbor, N.Y.
69. Santiago, B., U. Schübel, C. Egelseer, and O. Meyer. 1999. Sequence analysis, characterization and CO-specific transcription
of the cox gene cluster on the megaplasmid pHCG3 of Oligotropha carboxidovorans. Gene 236:115-124.[CrossRef][Medline]
70. Schübel, U., M. Kraut, G. Mörsdorf, and O. Meyer. 1995. Molecular characterization of the gene cluster coxMSL encoding the
molybdenum-containing carbon monoxide dehydrogenase of Oligotropha carboxidovorans. J. Bacteriol. 177:2197-
2203.[Abstract]
71. Schuetzle D. Sampling of vehicle emissions for chemical analysis and biological testing. Environ Health Perspect 47:34-48
(1983).
72. SIS Flytande petroleumprodukter--Blyfri bensin--Specifikation Svensk Standard SS-EN 228. Sweden, 13 March 1991.
73. Smibert, R. M., and N. R. Krieg. 1994. Phenotypic characterization, p.607 -654. In P. Gerhardt, R. G. E. Murray, W. A. Wood,
and N. R. Krieg (ed.), Methods for general and molecular bacteriology. American Society for Microbiology, Washington, D.C.
74. Stenberg U, Alsberg T, Westerholm R. Applicability of a cryogradient technique for the enrichment of PAH from automobile
exhausts: demonstration of methodology and evaluation experiments. Environ Health Perspect 47:43-51 (1983).
75. Stenberg U, Westerholm R, Alsberg T. Enrichment of gaseous compounds from diluted gasoline exhaust. A comparison
between adsorbent and cryogenic method. Environ Int 11:119-124 (1985).
76. Stump F, Bradow R, William R, Dropkin D, Zweidinger R, Sigsby S. Trapping gaseous hydrocarbons for mutagenic testing. SAE-
Paper No. 820776. Warrendale, PA:Society of Automotive Engineers, 1982.
77. Susuki T. Future diesel engines: problems, technologies, and challenges. In: Proceedings of the 11th Annual Energy-Sources
Technology Conference and Exhibition, 10-13 January 1988, New Orleans, LA, Calvin W. Rice Lecture.
78. Swedish Ministry of Communication. Data prepared for a Special Guidance Group (in Swedish). Stencil K (No. 2) 1968. Stencil K
(No. 1) 1971.
79. U.S. EPA. Diesel particulate control. Report No. SAE SP-240. Outline of supplemental rules and guidances for reformulated
gasoline, anti dumping, and oxygenated gasoline. United States Environmental Protection Agency, 1991.
80. Uchino, Y., A. Hirata, A. Yokota, and J. Sugiyama. 1998. Reclassification of marine Agrobacterium species: proposals of
Stappia stellulata gen. nov., comb. nov., Stappia aggregata sp. nov., nom. rev., Ruegeria atlantica, gen. nov., comb. nov.,
Ruegeria gelatinovora comb. nov., Ruegeria algicola comb. nov., and Ahrensia kieliense gen. nov., sp. nov., nom. rev. J. Gen.
Appl. Microbiol. 44:201-210.[Medline]
81. US Federal Register. Protection of Environment, Code of Federal Regulations parts 81-99, Revised as of 1 July 1986.
82. Wall J, Hoekman S. Fuel composition effects on heavy duty diesel particulate emissions. SAE Paper No. 841364. Warrendale,
PA:Society of Automotive Engineers, 1984.
83. Wall J, Shimpi S, Yu M. Fuel sulfur reduction for control of diesel particulate emissions. SAE Paper No. 872139. Warrendale,
PA:Society of Automotive Engineers, 1987.
84. Walsh M, Bradow R. Diesel particulate control around the world. SAE Paper No. 910130. Warrendale, PA:Society of Automotive
Engineers, 1990.
85. Watson, R. T., H. Rodhe, H. Oeschger, and U. Siegenthaler.1990 . Greenhouse gases and aerosols, p.1 -40. In J. T.
Houghton, G. J. Jenkins, and J. J. Ephraums (ed.), Climate change: the IPCC scientific assessment. Cambridge University
Press, Cambridge, United Kingdom.
86. Westerholm R, Almén J, Hang L, Rannug U, Egebäck K-E, Grägg K. Chemical and biological characterization of particulate,
semi volatile phase associated compounds in diluted heavy-duty diesel exhausts: a comparison of three different semi volatile
phase samplers. Environ Sci Technol 25:332-338 (1991).
87. Westerholm R, Almén J, Hang L, Rannug U, Rosen Å. Chemical analysis and biological testing of exhaust emissions from two
catalyst equipped light-duty vehicles operated at constant cruising speeds 70 and 90 km/hr and during acceleration conditions
from idling up to 70 and 90 km/hr. Total Environ 93:191-198 (1990).
88. Westerholm R, Almén J, Hang L, Rannug U, Rosen Å. Exhaust emissions from gasoline fueled light-duty vehicles operated in
different driving conditions: a chemical and biological characterization. Atmos Environ 26B:79-90 (1992).
22. 89. Westerholm R, Alsberg T, Frommelin Å, Strandell M, Rannug U, Winquist L, Grigoriadis V, Egebäck K-E. Effect of fuel polycyclic
aromatic hydrocarbon content on the emissions of polycyclic aromatic hydrocarbons and other mutagenic substances from a
gasoline-fueled automobile. Environ Sci Technol 22(8):925-930 (1988).
90. Westerholm R, Alsberg T, Strandell M, Frommelin Å, Grigoriadis V, Hantzaridou A, Maitra G, Winquist L, Rannug U, Egebäck K-
E, Bertilsson T. Chemical analysis and biological testing of emissions from a heavy duty diesel truck with and without two
different particulate traps. SAE Paper No. 860014. Warrendale, PA:Society of Automotive Engineers, 1986.
91. Westerholm R, Egebäck K-E, eds. Impact of fuels on diesel exhaust emissions: a chemical and biological characterization.
SwEPA Report No. 3968. Solna, Sweden:Swedish Environmental Protection Agency, 1991.
92. Westerholm R, Li Hang, Egebäck K-E, Grägg K. Exhaust emission reduction from a heavy-duty diesel truck, using a catalyst and
a particulate trap. FUEL 68:856-860 (1989).
93. Westerholm R, Stenberg U, Alsberg T. Some aspects on the distribution of polycyclic aromatic compounds between particles
and gas phase from diluted gasoline exhausts, and its importance for measurement in ambient air. Atmos Environ 22:1005-1010
(1988).
94. Westerholm R. A cryogradient sampling system for chemical analysis of polycyclic aromatic compounds (PAC). Studies of the
gas phase-emitted PAC from automobiles. Ph.D. Thesis. University of Stockholm, Stockholm, Sweden, 1988.
95. Westerholm R. Inorganic and organic compounds in emissions from diesel powered vehicles: a literature survey, Statens
Naturvårdsverk, SNV Report No. 3389. Stockholm:National Swedish Environmental Protection Board, 1987.
96. Wold S. Cross-validatory estimation of the number of components in factor and principal components models. Technometrics
20:397-406 (1978).
97. Zafiriou, O. C., S. S. Andrews, and W. Wang.2003 . Concordant estimates of oceanic carbon monoxide source and sink
processes in the Pacific yield a balanced global "blue-water" CO budget. Glob. Biogeochem. Cycles 17:1015.
98. Zelenka P, Kriegler PL, Herzog PL, Cartellieri WP. Ways towards the clean heavy-duty diesel. SAE Paper No. 900602.
Warrendale, PA: Society of Automotive Engineers, 1990.