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Inhalation Toxicology
International Forum for Respiratory Research
Volume 27, 2015 - Issue 11
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Research Article

Generation and characterization of diesel engine combustion emissions from petroleum diesel and soybean biodiesel fuels and application for inhalation exposure studies

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Pages 515-532 | Received 04 Mar 2015, Accepted 22 Jul 2015, Published online: 30 Oct 2015
 

Abstract

Biodiesel made from the transesterification of plant- and animal-derived oils is an important alternative fuel source for diesel engines. Although numerous studies have reported health effects associated with petroleum diesel emissions, information on biodiesel emissions are more limited. To this end, a program at the U.S. EPA assessed health effects of biodiesel emissions in rodent inhalation models. Commercially obtained soybean biodiesel (B100) and a 20% blend with petroleum diesel (B20) were compared to pure petroleum diesel (B0). Rats and mice were exposed independently for 4 h/day, 5 days/week for up to 6 weeks. Exposures were controlled by dilution air to obtain low (50 µg/m3), medium (150 µg/m3) and high (500 µg/m3) diesel particulate mass (PM) concentrations, and compared to filtered air. This article provides details on facilities, fuels, operating conditions, emission factors and physico-chemical characteristics of the emissions used for inhalation exposures and in vitro studies. Initial engine exhaust PM concentrations for the B100 fuel (19.7 ± 0.7 mg/m3) were 30% lower than those of the B0 fuel (28.0 ± 1.5 mg/m3). When emissions were diluted with air to control equivalent PM mass concentrations, B0 exposures had higher CO and slightly lower NO concentrations than B100. Organic/elemental carbon ratios and oxygenated methyl esters and organic acids were higher for the B100 than B0. Both the B0 and B100 fuels produced unimodal-accumulation mode particle-size distributions, with B0 producing lower concentrations of slightly larger particles. Subsequent papers in this series will describe the effects of these atmospheres on cardiopulmonary responses and in vitro genotoxicity studies.

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Acknowledgements

The authors are grateful to H. de Weerd and H. Makarem (TNO, Netherlands) for their help with the analysis of the 32 PAHs and to Drs Mike Madden and Andy Miller for careful review of the article. The research described in this article has been reviewed by the U.S. EPA National Health and Environmental Effects Research Laboratory and approved for publication. The contents of this article should not be construed to represent Agency policy nor does mention of trade names or commercial products constitute endorsement or recommendation for use.

Declaration of interest

Portions of this work were sponsored under the EPA/DOE interagency agreement DW-89-92298301 with Oak Ridge Institute for Science and Education (ORISE). The authors report no declarations of interest.

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