Yii Leng Chan

The Comparative and Combined Effects of Nitric Oxide and Higher Alkanes in Sensitizing Methane Oxidation

The comparative and combined effects of nitric oxide (NO) and higher alkanes on methane oxidation were examined by experimentation and kinetic modeling. Experiments were conducted using fuel-lean, lower-alkanes mixtures with NO (0–400 ppm v/v) in an atmospheric flow reactor at residence time of 2 s over the temperature range of 820–950 K. NO was found to greatly promote methane conversion, and its sensitizing effect strengthened with the increasing concentration that was added to the system. The promoting effect of higher alkanes on methane conversion was also evident, particularly at zero or low NO concentrations. A strong dependency of the sensitizing effect on the concentration of higher alkanes present was also observed. The kinetic mechanism from Le Cong et al., performed reasonably well in reproducing the experimental trends. However, the sensitizing propensity of higher alkanes in the presence of NO could not be unambiguously ranked under all conditions. Modification to the kinetic mechanism of Le Cong et al., was attempted. Specifically, the submechanism of C3 peroxy radicals was added, but the modeling results indicated a lower impact on methane conversion than was initially expected. The most sensitive reactions were revealed, and the generalized reaction pathways for methane oxidation sensitized by higher alkanes, with or without the presence of NO, were also proposed, following detailed sensitivity analysis.

A Preliminary High-Pressure Thermogravimetric Study of Combustion Reactivity of a Collie Coal Char

The effect of pressure(up to 20 bar)on the reactivity of a char(150–160 μm) produced from Western Australian Collie coal has been studied using a high-pressure thermogravimetric analyser (HP TGA). The pressure demonstrated a positive effect in enhancing char combustion reactivities.Kinetic parameters have been determined from the experimental data.The apparent reaction order was found to be approximately 0.7 and the apparent activation energies were 91.0 kJ/mol at atmospheric pressure and 1.5 kJ/mol at an elevated pressure(10 bar),indicating a shift in the control regimes of the reaction at elevated pressures.The lumped effect of the sample size, bulk diffusion,interparticle and intraparticle diffusion at the elevated pressures played an important role in reducing the mass transfer during the HP-TGA experimentation.Thus the activation energy calculated at elevated pressures may not represent the intrinsic activation energy of the char particles but the apparent values of the bulk of the samples.