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A quasi-steady 1-dimensional computer model of a catalyzed particulate filter (CPF) capable of simulating active regeneration of the CPF via diesel fuel injection upstream of a diesel oxidation catalyst (DOC) or other means to increase the exhaust gas temperature has been developed. This model is capable of predicting gaseous species concentrations (HC's, CO, NO and NO2) and exhaust gas temperatures within and after the CPF, for given input values of gaseous species and PM concentrations before the CPF and other inlet variables such as time-varying temperature of the exhaust gas at the inlet of the CPF and volumetric flow rate of exhaust gas.

A 2007 Cummins ISL 8.9L direct-injection common rail diesel engine rated at 272 kW (365 hp) was used to load the filter to 2.2 g/L and passively oxidize particulate matter (PM) within a 2007 OEM aftertreatment system consisting of a diesel oxidation catalyst (DOC) and catalyzed particulate filter (CPF). Having a better understanding of the passive NO₂ oxidation kinetics of PM within the CPF allows for reducing the frequency of active regenerations (hydrocarbon injection) and the associated fuel penalties. Being able to model the passive oxidation of accumulated PM in the CPF is critical to creating accurate state estimation strategies. The MTU 1-D CPF model will be used to simulate data collected from this study to examine differences in the PM oxidation kinetics when soy methyl ester (SME) biodiesel is used as the source of fuel for the engine.

Passive regeneration (oxidation of particulate matter without using an external energy source) of particulate filters in combination with active regeneration is necessary for low load engine operating conditions. For low load conditions, the exhaust gas temperatures are less than 250°C and the PM oxidation rate due to passive regeneration is less than the PM accumulation rate. The objective of this research was to experimentally investigate active regeneration of a catalyzed particulate filter (CPF) using diesel fuel injection in the exhaust gas after the turbocharger and before a diesel oxidation catalyst (DOC) and to collect data for extending the MTU 1-D 2-layer model to include the simulation of active regeneration. The engine used in this study was a 2002 Cummins ISM turbo charged 10.8 L heavy duty diesel engine with cooled EGR. The exhaust after-treatment system consisted of a Johnson Matthey DOC and CPF (a CCRT®).

Active regeneration experiments were carried out on a production 2007 Cummins 8.9L ISL engine and associated diesel oxidation catalyst (DOC) and catalyzed particulate filter (CPF) aftertreatment system. The effects of SME biodiesel blends were investigated to determine the particulate matter (PM) oxidation reaction rates for active regeneration. The experimental data from this study will also be used to calibrate the MTU-1D CPF model [1]. The experiments covered a range of CPF inlet temperatures using ULSD, B10, and B20 blends of biodiesel. The majority of the tests were performed at a CPF PM loading of 2.2 g/L with in-cylinder dosing, although 4.1 g/L and a post-turbo dosing injector were also investigated. The PM reaction rate was shown to increase with increasing percent biodiesel in the test fuel as well as increasing CPF temperature.

A model for calculating the trap pressure drop, particulate mass inside the trap and various particulate and trap properties was developed using the steady-state data and the theory developed by Konstandopoulos & Johnson, 1989. Changes were made with respect to the calculation of clean pressure drop, particulate layer porosity and the particulate layer permeability. This model was validated with the data obtained from the steady-state data run with different traps supplied by Corning Inc. The data were collected using the 1988 Cummins L-10 heavy-duty diesel engine using No.2 low sulfur diesel fuel. The three different traps were EX 80 (100 cell density), EX 80 (200 cell density) and EX 66 (100 cell density) all with a 229 mm diameter and 305 mm length. These traps were subjected to different particulate matter loadings at different speeds. The traps were not catalyzed.