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HCl and SO{sub 2} simultaneous absorption at 1023 K with calcined limestone

Conference ·
OSTI ID:355840
; ;  [1]; ;  [2]
  1. Osaka Univ., Toyonaka, Osaka (Japan). Dept. of Chemical Engineering
  2. NKK Corp., Kawasaki, Kanagawa (Japan)

In order to understand sorbent performance for co-combustion of coal and wastes such as refused derived fuel, simultaneous absorption of HCl and SO{sub 2} with calcined limestone was fundamentally investigated using a thermogravimetry at 1,023 K. SO{sub 2} absorption was interestingly accelerated in the presence of HCl and the level of conversion of calcined limestone reached almost 100% even when particles with 710--1,000 {micro}m of diameter were used. The mechanisms of this increase in absorption capacity were discussed mainly based on the results of scanning electron microscopic and energy dispersive analysis of X-ray observations, and differential scanning calorimetry. As a result, it was concluded that a molten phase was formed on limestone surface in the early stage of reaction and this phase spread into the bulk with the progress of reaction. Melting point was lowered to ca. 998 K by formation of a eutectic phase of CaSO{sub 4} and CaCl{sub 2} mixture. It was considered that such a molten phase caused the absorption capacity increase observed for simultaneous absorption of HCl and SO{sub 2} with calcined limestone.

OSTI ID:
355840
Report Number(s):
CONF-9705116--; ISBN 0-7918-1557-9
Country of Publication:
United States
Language:
English