The kinetics of the NO-carbon reaction was studied by thermogravimetric analysis (TGA). The reactivity as a function of carbon conversion was systematically investigated through characterization of the pore structure and carbon active site evolution during reaction. Total surface area measured by CO2 adsorption at 273 K gives a relatively constant normalized reactivity over a wide range of carbon conversions. The carbon active surface area (ASA) and unoccupied active surface area (UASA) were estimated from low-temperature NO chemisorption capacities. Large amounts of stable C-O complexes are found to form during the reaction. Results show that ASA or UASA measured in this way do not represent the reactive surface area under gasification conditions. A new kinetic model is introduced by taking into account the contributions from different carbon-oxygen surface complexes during reaction, based on the recently proposed unified kinetic scheme of Yang and coworkers.
|Original language||English (US)|
|Number of pages||12|
|Journal||Chemical Engineering Science|
|State||Published - Jun 25 1999|
All Science Journal Classification (ASJC) codes
- Chemical Engineering(all)
- Industrial and Manufacturing Engineering