TY - JOUR
T1 - Thermal abatement of nitrogen-containing hydrocarbons by non-catalytic supercritical water oxidation (SCWO)
AU - Al-Duri, Bushra
AU - Pinto, L
AU - Ashraf-Ball, NH
AU - Santos, Regina
PY - 2008/2/1
Y1 - 2008/2/1
N2 - This work investigated the destruction of N-containing hydrocarbons namely DBU (1,8-diazobicyclo[5.4.0]undec-7-ene) and DMF (dimethyl formamide) by supercritical water oxidation (SCWO), using hydrogen peroxide as oxidant. Reactions were conducted under temperatures of (400-650 degrees C), pressures of (50-250 bars), oxidant stoichiometric ratio SR (0.9-12), initial concentrations of organics (0.1-8.4 mM) and residence time tau (6-17 s). Reactions took place in a plug flow continuous reactor and the results were presented in terms of the % removal (of TOC and the organic compound), C-fraction and N-fraction; all plotted as function of the above system conditions. Also, GC-MS analysis for DMF was conducted. Percent removal increased with temperature and complete organic- and > 90% TOC removal, was obtained at 500 and 600 degrees C for DMF and DBU respectively. Conversion increased with the oxidant SR, residence time and initial organic concentration. Pressure affected conversion in the sub- and near-critical conditions but not in the supercritical region, yet an initial value of 150 bar was required to start the reaction. Pseudo first order-, integral power rate law-, and power law models successfully described the kinetic data; and the reaction constants for each model and energy of activation were evaluated.
AB - This work investigated the destruction of N-containing hydrocarbons namely DBU (1,8-diazobicyclo[5.4.0]undec-7-ene) and DMF (dimethyl formamide) by supercritical water oxidation (SCWO), using hydrogen peroxide as oxidant. Reactions were conducted under temperatures of (400-650 degrees C), pressures of (50-250 bars), oxidant stoichiometric ratio SR (0.9-12), initial concentrations of organics (0.1-8.4 mM) and residence time tau (6-17 s). Reactions took place in a plug flow continuous reactor and the results were presented in terms of the % removal (of TOC and the organic compound), C-fraction and N-fraction; all plotted as function of the above system conditions. Also, GC-MS analysis for DMF was conducted. Percent removal increased with temperature and complete organic- and > 90% TOC removal, was obtained at 500 and 600 degrees C for DMF and DBU respectively. Conversion increased with the oxidant SR, residence time and initial organic concentration. Pressure affected conversion in the sub- and near-critical conditions but not in the supercritical region, yet an initial value of 150 bar was required to start the reaction. Pseudo first order-, integral power rate law-, and power law models successfully described the kinetic data; and the reaction constants for each model and energy of activation were evaluated.
UR - https://www.scopus.com/pages/publications/37849003474
U2 - 10.1007/s10853-007-2285-3
DO - 10.1007/s10853-007-2285-3
M3 - Article
SN - 1573-4803
VL - 43
SP - 1421
EP - 1428
JO - Journal of Materials Science
JF - Journal of Materials Science
IS - 4
ER -