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The role of NO2 and NO in the mechanism of hydrocarbon degradation leading to carbonaceous deposits in engines

Accepted version
Peer-reviewed

Type

Article

Change log

Authors

Slavchov, RI 
Russo, D 
Salama, I 
Mosbach, S 

Abstract

© 2020 Elsevier Ltd A hypothetical mechanism of degradation of the fuel droplet leaking out from the injector nozzle in a direct injection combustion engine has been proposed recently. This involves as a key step a radical chain oxidation initiated by NO2 and branched by nitric oxide, NO, both produced by the combustion. The degradation causes the formation of injector nozzle carbonaceous deposits. The present work gives an experimental validation of some of the assumptions behind this model. An autoclave is used to oxidize isooctane under conditions relevant to the cylinder wall near the nozzle (~150 °C, 10 bar, 5% O2, 100 ppm of NO2 by mole and 500 ppm NO in the gas phase), and the degradation products are monitored via gas chromatography-mass spectrometry (GC–MS). The results show no observable fuel degradation in the absence of NOx. NO appears to be able to initiate a radical chain by producing NO2. Nitric oxide also alters the radical chain by transforming the alkyl peroxy radicals (ROO⋅) to more reactive alkoxy radicals (RO⋅), resulting in a range of different products. In addition, NO tends to terminate the radical chain by neutralizing a fraction of the alkyl peroxy radicals, producing alkyl nitrates as termination products. The existence of a radical chain is supported by demonstrating the antioxidative action of a radical scavenger. The chemical reaction mechanism is investigated, based on the detected products, and the key species involved in the degradation process are identified.

Description

Keywords

Engine deposits, NOx, Autooxidation, Gasoline, Radical chain, Anti-oxidant

Journal Title

Fuel

Conference Name

Journal ISSN

0016-2361
1873-7153

Volume Title

267

Publisher

Elsevier BV
Sponsorship
The funding and technical support from BP through the BP International Centre for Advanced Materials (BP-ICAM) made this research possible. The work was partly funded by the National Research Foundation (NRF), Prime Minister’s Office, Singapore under its Campus for Research Excellence and Technological Enterprise (CREATE) programme. Markus Kraft gratefully acknowledges the support of the Alexander von Humboldt foundation.