NO RELEASE AND REACTIVITY OF CHARS DURING COMBUSTION - THE EFFECT OF DEVOLATILIZATION TEMPERATURE AND HEATING RATE

Citation
Wx. Wang et al., NO RELEASE AND REACTIVITY OF CHARS DURING COMBUSTION - THE EFFECT OF DEVOLATILIZATION TEMPERATURE AND HEATING RATE, Energy & fuels, 10(2), 1996, pp. 409-416
Citations number
50
Categorie Soggetti
Engineering, Chemical","Energy & Fuels
Journal title
ISSN journal
08870624
Volume
10
Issue
2
Year of publication
1996
Pages
409 - 416
Database
ISI
SICI code
0887-0624(1996)10:2<409:NRAROC>2.0.ZU;2-1
Abstract
The study has involved the investigation of the influence of pyrolysis heat treatment temperature (HTT) and heating rate on the reactivity a nd the release of char-N during temperature-programmed combustion (TPC ) of a set of wire mesh reactor chars in a thermogravimetric analyzer- mass spectrometer system. The gas evolution profiles are bimodal and t his indicates the presence of species of different reactivity. It was found that increasing pyrolysis temperature and heating rate both prod uced significant variation in the reactivity of the resultant chars wi th the former being more influential. This is apparent from the shift of peak positions and the change in the relative intensity of the low- and high-temperature peaks of CO, CO2, and NO evolution profiles. The differences in the CO2 and NO evolution profiles observed between the Gedling entrained flow reactor (EFR) and wire mesh reactor (WMR) char s of similar heat treatment temperatures may be explained by the diffe rent extents of pyrolysis experienced by the chars. However, chars pro duced in the WMR with pyrolysis temperatures up to 1200 degrees C show little variation in the char-N conversion to NO. This is believed to be due to the highly reactive nature of the chars which give rise to a high extent of reduction of the primary product NO formed during gasi fication leading to a low NO/char-N ratio. Heat treatment of the chars at lower heating rates and longer soak times to temperatures in the r ange 1100-1400 degrees C lead to reduced char reactivity and higher NO /char-N ratios under temperature-programmed combustion conditions. The results are consistent with the reduction of the primary oxidation pr oduct NO on the surface and in the pores of the char.