Regeneration of Fe₂O₃-based high-temperature coal gas desulfurization sorbent in atmosphere with sulfur dioxide

Abstract

Regeneration of a high-temperature coal gas desulfurization sorbent is a key technology in its industrial applications. A Fe₂O₃-based high-temperature coal gas desulfurizer was prepared using red mud from steel factory. The influences of regeneration temperature, space velocity and regeneration gas concentration in SO₂ atmosphere on regeneration performances of the desulfurization sorbent were tested in a fixed bed reactor. The changes of phase and the composition of the Fe₂O₃-based high-temperature coal gas desulfurization sorbent before and after regeneration were examined by X-ray diffraction(XRD) and X-ray Photoelectron spectroscopy(XPS), and the changes of pore structure were characterized by the mercury intrusion method. The results show that the major products are Fe₃O₄ and elemental sulfur; the influences of regeneration temperature, space velocity and SO₂ concentration in inlet on regeneration performances and the changes of pore structure of the desulfurization sorbent before and after regeneration are visible. The desulfurization sorbent cannot be regenerated at 500°C in SO₂ atmosphere. Within the range of 600°C – 800°C, the time of regeneration becomes shorter, and the regeneration conversion increases as the temperature rises. The time of regeneration also becomes shorter, and the elemental sulfur content of tail gas increases as the SO₂ concentration in inlet is increased. The increase in space velocity enhances the reactive course; the best VSP is 6000 h^-1 for regeneration conversion. At 800°C, 20 vol-% SO₂ and 6000 h^-1, the regeneration conversion can reach nearly to 90%.

Keywords

high-temperature coal gas, Fe₂O₃ desulfurization sorbent, SO₂ atmosphere, regeneration behaviors / sulfur recovery

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Acknowledgments

This project was supported by the National Basic Research Program of China (Grant No. 2005CB221203) and the Shanxi Province Key Technologies R & D Program (No. 20080322035).

RIGHTS & PERMISSIONS

2014 Higher Education Press and Springer-Verlag Berlin Heidelberg