The kinetics of the NO-carbon reaction was studied by thermogravimetric ana
lysis (TGA). The reactivity as a function of carbon conversion was systemat
ically investigated through characterization of the pore structure and carb
on active site evolution during reaction. Total surface area measured by CO
, adsorption at 273 K gives a relatively constant normalized reactivity ove
r a wide range of carbon conversions. The carbon active surface area (ASA)
and unoccupied active surface area (UASA) were estimated from low-temperatu
re NO chemisorption capacities. Large amounts of stable C-O complexes are f
ound to form during the reaction. Results show that ASA or UASA measured in
this way do not represent the reactive surface area under gasification con
ditions. A new kinetic model is introduced by taking into account the contr
ibutions from different carbon-oxygen surface complexes during reaction, ba
sed on the recently proposed unified kinetic scheme of Yang and coworkers.
(C) 1999 Elsevier Science Ltd. All rights reserved.