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The transport sector is one of the major contributors to greenhouse gas emissions. This study investigated three greenhouse gases emitted from road transport using a probe vehicle: CO₂, N₂O and CH₄ emissions as a function temperature. It should be highlighted that methane is a greenhouse gas that similarly to carbon dioxide contributes to global warming and climate change. An oxidation catalyst was used to investigate CO₂, N₂O and CH₄ GHG emissions over a real-world driving cycle that included urban congested traffic and extra-urban driving conditions. The results were determined under hot start conditions, but in congested traffic the catalyst cooled below its light-off temperature and this resulted in considerable N₂O emissions as the oxidation catalyst temperature was in the N₂O formation band. This showed higher N₂O during hot start than for diesel fuel and B100 were compared. The B100 fuel was Fatty Acid Methyl Ester (FAME), derived from waste cooking oil, which was mainly RME.

An on-board emission measurement system (PEMS), the Horiba OBS 1300, was installed in Euro 1-4 SI cars of the same model to investigate the impact of vehicle technology on exhaust emissions, under urban driving conditions with a fully warmed-up catalyst. A typical urban driving loop cycle was used with no traffic loading so that driver behavior without the influence of other traffic could be investigated. The results showed that under real world driving conditions the NOx emissions exceeded the legislated values and only at cruise was the NOx emissions below the legislated value. The higher NOx emissions during real-world driving have implications for higher urban Ozone formation. With the exception of the old EURO1 vehicle, HC and CO emissions were under control for all the vehicles, as these are dominated by cold start issues, which were not included in this investigation.

Rape oil, as used in fresh cooking oil (FCO), and the methyl ester derived from waste cooking oil (WCOB100) were tested as 100% biofuels (B100) on a heavy duty DI diesel engine under steady state conditions. The exhaust emissions were measured and compared to those for conventional low sulphur (<50ppm) diesel fuel. The engine used was a 6 cylinder, turbocharged, intercooled Perkins Euro2 Phaser Engine, fitted with an oxidation catalyst. The engine out gaseous emissions results for WCOB100 showed a large decrease in CO and HC emissions, but a small increase in NOx emissions compared to diesel. However, for FCO the CO and HC increased relative to WCOB100 and CO was higher than for diesel, indicating deterioration in fuel/air mixing. The particulate matter (PM) emissions for WCOB100 were similar to those for diesel at the 23kw condition, but greatly reduced at 47kw. The FCO produced higher engine out PM at both power conditions due to a higher volatile organic fraction (VOF).

Condensable and gaseous hydrocarbon emissions and speciation of the hydrocarbons have been investigated using a EURO1 emissions compliant SI (Spark Ignition) car. Exhaust gas samples were simultaneously collected upstream and downstream of the catalyst using a system containing cold ice trap, resin, particulate filter block and Teflon gas sampling bag. GC (Gas Chromatography) was employed to analyze for hydrocarbons and 16 of the more significant hydrocarbons are reported. The test was carried out using both cold start and hot start driving cycles. Results show that the benzene and toluene were major species emitted from the tailpipe under cold start conditions. Methylnaphthalene was a dominated hydrocarbon under hot start conditions. The cold start had significant influence on hydrocarbon emissions. The catalyst out benzene emissions for cold start was thirty times higher than that for hot start.

A precision in-vehicle tail-pipe emission measurement system was installed in a EURO1 emissions compliant SI car and used to investigate the variability in tail-pipe emission generation at an urban traffic junction. Exhaust gas and skin temperatures were also measured along the exhaust pipe of the instrumented vehicle, so the thermal characteristics and the efficiency of the catalyst monitored could be included in the analysis. Different turning movements (driving patterns) at the priority T-junction were investigated such as straight, left and right turns with and without stops. The test car was hot stable running conditions before each test, thereby negating cold start effects. To demonstrate the influence of the junction on tail-pipe emissions and fuel consumption, distance based factors were determined that compared the intersection drive-through measurements with steady speed (state) runs. Fuel consumption was increased at intersections by a factor of 1.3∼5.9.

The objective of this work was the development of an on-road in-vehicle emissions measurement technique utilizing a relatively new, commercial, portable Fourier Transform Infra-Red (FTIR) Spectrometer capable of identifying and measuring (at approximately 3 second intervals) up to 51 different compounds. The FTIR was installed in a medium class EURO1 spark ignition passenger vehicle in order to measure on-road emissions. The vehicle was also instrumented to allow the logging of engine speed, road speed, global position, throttle position, air-fuel ratio, air flow and fuel flow in addition to engine, exhaust and catalyst temperatures. This instrumentation allowed the calculation of mass-based emissions from the volume-based concentrations measured by the FTIR. To validate the FTIR data, the instrument was used to measure emissions from an engine subjected to a real-world drive cycle using an AC dynamometer.

The influence of ambient temperature on exhaust emissions for an instrumented Euro 1 SI car was determined for urban congested traffic conditions. In UK cities cold-starting vehicles directly into congested traffic conditions is a common occurrence that is not currently taken into account when modeling urban traffic pollution. In-vehicle emission samples were taken directly from the exhaust, upstream and downstream of the catalyst, using the bag sampling technique. The first bag was for the cold start emissions and approximately the first 1.1 km of travel. The following three bags were with a hotter catalyst. The cold start tests were conducted over a year, with ambient temperatures ranging from 2°C to 30°C. The results showed that CO emissions for the cold start were reduced by 70% downstream of the catalyst when the ambient temperature rose from 2°C to 30°C. The corresponding hydrocarbon emissions were reduced by 41% and NOx emissions were increased by 90%.

The influence of ambient temperature on exhaust emissions for an instrumented Euro 1 SI car was determined. A real world test cycle was used, based on an urban drive cycle that was similar to the ECE urban drive cycle. It was based on four laps of a street circuit and an emissions sample bag was taken for each lap. The bag for the first lap was for the cold start emissions. An in-vehicle direct exhaust dual bag sampling technique was used to simultaneously collect exhaust samples upstream and downstream of the three-way catalyst (TWC). The cold start tests were conducted over a year, with ambient temperatures ranging from - 2°C to 32°C. The exhaust system was instrumented with thermocouples so that the catalyst light off temperature could be determined. The results showed that CO emissions for the cold start were reduced by a factor of 8 downstream of catalyst when ambient temperature rose from -2°C to 32°C, the corresponding hydrocarbon emissions were reduced by a factor of 4.

The influence of a diesel oxidation catalyst and a practical exhaust system with two silencers on the storage and release of particulates during cold start real world driving was investigated using a Ford 1.8 litre IDI Mondeo diesel passenger car. Particulates were sampled simultaneously at three points in the exhaust using an on-board gravimetric filter paper method. The test was carried out on two different on-road driving cycles: a simulated ECE 15 cycle to represent free moving low power city driving conditions, and a traffic jam and high speed suburban driving cycle. The results showed that the particulate matter was deposited in the oxidation catalyst during cold start and deposited in the exhaust system downstream of the catalyst throughout the test period. The particulate deposition and release downstream of the catalyst were influenced by the previous operational history of the vehicle.

The solvent organic fraction (SOF) of particulates from the exhaust pipe of a diesel engine, a dilution tunnel and a roadside sample are compared. Three different techniques of SOF analysis are also compared, vacuum oven, solvent extraction and pyroprobe/GC. Gaseous hydrocarbons and the methane contribution were measured in the exhaust pipe throughout the speed and load range of the engine at 185 C and 2 C. The unburnt hydrocarbons decreased with air/fuel ratio for all speeds and there was an overall decrease in emissions with increasing speed. The differential temperature technique showed the maximum mass of hydrocarbon which could condense from the gas phase onto the particulate as the SOF. The method compared well with the actual SOF of the tunnel particulate.