Abstract
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) |
---|---|
Pages (from-to) | 4125-4136 |
Number of pages | 12 |
Journal | Chemical Engineering Science |
Volume | 54 |
Issue number | 19 |
DOIs | |
State | Published - Jun 25 1999 |
All Science Journal Classification (ASJC) codes
- General Chemistry
- General Chemical Engineering
- Industrial and Manufacturing Engineering