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The European research co-operation Lotus is presented. The main objectives of the project were i) to show the potential for a urea-based SCR system to comply with the EU standard of years 2005 and 2008 for heavy-duty Diesel engines for different driving conditions with optimal fuel consumption, ii) to reach 95 % conversion of NOx at steady state at full load on a Euro III engine, iii) to reach 75 % NOx reduction for exhaust temperatures between 200-300°C, and 85 % average NOx reduction between 200-500°C. The energy content of the consumed urea should not exceed 1.0 %, calculated as specific fuel consumption. These targets were met in May 2003 and the Lotus SCR system fulfilled the Euro V NOx legislative objectives for year 2008.

In a consortium of European industrial partners and research institutes, a combination of industrial development and scientific research was organised. The objective was to improve the catalytic NOx conversion for lean burn cars and heavy-duty trucks, taking into account boundary conditions for the fuel consumption. The project lasted for three years. During this period parallel research was conducted in research areas ranging from basic research based on a theoretical approach to full scale emission system development. NOx storage catalysts became a central part of the project. Catalysts were evaluated with respect to resistance towards sulphur poisoning. It was concluded that very low sulphur fuel is a necessity for efficient use of NOx trap technology. Additionally, attempts were made to develop methods for reactivating poisoned catalysts. Methods for short distance mixing were developed for the addition of reducing agent.

In a joint research project between industrial companies and a number of research institutes, nitrogen oxide conversion in oxygen containing exhaust gas has been investigated according to the following procedure Basic investigations of elementary steps of the chemical reaction Production and prescreening of different catalytic material on laboratory scale Application oriented screening of industrial catalyst material Catalyst testing on a lean bum gasoline engine, passenger car diesel engines (swirl chamber and DI) and on a DI truck engine Although a number of solid body structures show nitrogen oxide reduction by hydrocarbons, only noble metal containing catalysts and transition metal exchanged zeolites gave catalytic efficiencies of industrial relevance. A maximum of 25 % NOx reduction was found in the European driving cycle for passenger cars, about 40 % for truck engines in the respective European test.

The reactions over a commercially available double layer tri-metal type (Pt, Pd, Rh) passenger car catalyst were analysed. A parameter study was performed in synthetic exhaust gases at: steady state conversion, periodic oscillations, and controlled transients. The influences of gas phase composition, temperature, adiabatic heat of reaction and lambda oscillations were investigated. The reactions of nitrogen oxides, propene and carbon monoxide were simultaneously analysed. Fast response emission analysers were used to record the dynamic properties of the catalysts. The catalyst was found to have high conversion rates and high oxygen storage capacity at relatively low temperatures. The presence of sulphur dioxide was found to reduce the conversion of CO and NOx substantially. An emission increase of 40-70 % was observed for steady state conditions and at oscillating conditions the increase was more than 100%.

The formation of Nitrous Oxide (N2O) over an aged three way catalyst was analysed in a laboratory reactor for a variety of simulated Otto engine exhaust gas conditions. Nitrous Oxide formation was further analysed during FTP75 dynamometer test with a car. The car was equipped with either an aged catalyst or a fresh one. A fast response diode laser system was modified to enable detection of Nitrous Oxide and Carbon Monoxide simultaneously. From laboratory data the kinetics of Nitrous Oxide formation were evaluated with mathematical simulations and a mechanism was suggested. The results were compared to data from vehicle tests and the results were discussed in the light of the laboratory study. Two general trends were confirmed, i) N2O formation increases at slightly lean conditions: ii) catalysts with a low degree of deterioration gave lower N2O emissions, iii) the extent of N2O formation goes though a maximum with respect to dissociation rate of NO.

Five field-aged catalysts with different mileages were analysed with respect to emission performance and structural changes. The FTP-75 emission results were compared to synthetic exhaust gas tests including: i) light-off, ii) lambda screening at stationary and oscillating stoichiometry, iii) space velocity variation. Several samples from different positions of one catalyst were used to achieve the spatially resolved activity profile for that catalyst. Surface characterisation was used to characterise accumulated catalyst poison. Laboratory space velocity test was concluded to be a sensitive probe for catalyst performance: good correlation to vehicle emission data was found. An analysis of the influence of temperature and λ oscillation on the catalyst conversion performance was made, with particular emphasis on the ageing effects.

Catalysts aged under different on-road conditions were analysed with respect to their conversion of CO and HC at step changes of the synthetic exhaust gas composition. Time resolved diode laser spectroscopy and fast response FID analysis were used to characterise the catalyst response to transient changes of CO and hydrocarbons in the exhaust gas. The oxygen storage capacity was monitored at various conditions; flow rate, catalyst temperature, previous exposure to oxidizing or reducing atmosphere and amplitude of the perturbation. The technique appeared to provide a sensitive probe for analysis of the dynamic oxygen storage capacity of new and aged catalysts at exhaust like conditions. The results correlate well with the transient emission performance during vehicle tests. Further, surface characterization using SEM/EDS and XPS techniques indicated that phosphate formation was the most probable cause of deactivation.

Four samples from each of two field-aged catalysts subjected to different field test conditions were investigated. The light-off and conversion performance of each sample was measured in a synthetic exhaust flow reactor system. Time-resolved laser IR spectroscopy was used to investigate the catalyst behaviour under transient conditions. Significant differences in light-off temperatures and transient conversion performance between the samples was observed. The samples taken from the inlet side of the monolith were more deactivated than the corresponding ones from the outlet. However, samples taken from peripheral positions always showed better performance than samples originating from the centre. In order to explain observed variations in activity, the following surface properties were examined: oxygen uptake, specific metal area (CO chemisorption), total surface area (BET) and chemical composition (XPS analysis).