Abstract

The purpose of this study is to explain how plasma improves the performance of selective catalytic reduction (SCR) of nitrogen oxides (NOx) with a hydrocarbon reducing agent. In the plasma-coupled SCR process, NOx reduction was performed with n-heptane as a reducing agent over Ag/γ-Al2O3 as a catalyst. We found that the plasma decomposes n-heptane into several oxygen-containing products such as acetaldehyde, propionaldehyde and butyraldehyde, which are more reactive than the parent molecule n-heptane in the SCR process. Separate sets of experiments using acetaldehyde, propionaldehyde and butyraldehyde, one by one, as a reductant in the absence of plasma, have clearly shown that the presence of these partially oxidized compounds greatly enhanced the NOx conversion. The higher the discharge voltage, the more the amounts of such partially oxidized products. The oxidative species produced by the plasma easily converted NO into NO2, but the increase of the NO2 fraction was found to decrease the NOx conversion. Consequently, it can be concluded that the main role of plasma in the SCR process is to produce partially oxidized compounds (aldehydes), having better reducing power. The catalyst-alone NOx removal efficiency with n-heptane at 250 °C was measured to be less than 8%, but it increased to 99% in the presence of acetaldehyde at the same temperature. The NOx removal efficiency with the aldehyde reducing agent was higher as the number of carbons in the aldehyde was more; for example, the NOx removal efficiencies at 200 °C with butyraldehyde, propionaldehyde and acetaldehyde were measured to be 83.5%, 58.0% and 61.5%, respectively, which were far above the value (3%) obtained with n-heptane.

Highlights

  • Nitrogen oxides (NOx ), together with volatile organic compounds (VOCs), are the main contributors to the generation of particulate matters or photochemical smog [1]

  • Most of the catalysts used for the removal of NOx from exhaust gases have excellent activity at high temperatures of 250–450 ◦ C [6,7,8], but the catalytic activity sharply decreases at lower temperatures

  • In the present catalytic NOx reduction system with Ag/γ‐Al2O3, the NOx conversion was by 30–80%, depending on whether plasmawith was generated the catalyst bed or not

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Summary

Introduction

Nitrogen oxides (NOx ), together with volatile organic compounds (VOCs), are the main contributors to the generation of particulate matters or photochemical smog [1]. Most of the catalysts used for the removal of NOx from exhaust gases have excellent activity at high temperatures of 250–450 ◦ C [6,7,8], but the catalytic activity sharply decreases at lower temperatures. Many researchers have made great efforts to improve catalytic NOx reduction performances at low temperatures [9,10,11,12]. When the temperature of exhaust gas fluctuates, it is very important to improve low-temperature catalytic activity to maintain a stable NOx reduction efficiency. In order to improve the NOx reduction performance at low temperatures, a method of enhancing the reactivity in the catalyst by changing the NO/NO2 ratio of the exhaust gas [11,12], or a method of improving the low-temperature catalytic activity by combining non-thermal plasma

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