The effects of hydrocarbons and water vapor on a combined deNO
x process, which consists of nonthermalplasma oxidation and V
2O
5-WO
3/TiO
2 selective catalytic reduction (SCR), are investigated. Test resultsshow that the fast SCR reaction, which needs equimolar amounts of NO and NO
2, plays a dominant role inreducing NO
x under relatively low-temperature conditions, i.e., 150-200
C. Under such low-temperatureconditions, the oxidation of NO to NO
2 induced by nonthermal plasma is useful in controlling NO
2 fractionsin NO
x for the fast SCR reaction. The role of the fast SCR reaction, however, decreases when C
3H
6 is suppliedto the process as simulated hydrocarbons in diesel exhausts. Test results yielded the following conclusions:(1) C
3H
6 leads to the production of aldehydes in the nonthermal plasma reactor. (2) The NO
2 fraction in theSCR reactor decreases as a result of aldehyde production, leading to a diminished role of the SCR reaction.This reduction in NO
2 is predominant when water vapor is not added to the test gases. (3) The decreased roleof the fast SCR reaction is recovered when water vapor is present in the treated gases, and the optimal NO
2fraction for peak deNO
x conversion shifts to higher fractions (greater than 0.5), which should be consideredin treating diesel exhaust.