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Lee, Kang Soo
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Mechanisms of direct and in-direct sulfation of limestone

Author(s)
Jeong, SeonghaLee, Kang SooKeel, Sang InYun, Jin HanKim, Yong JinKim, Sang Soo
Issued Date
2015-12
DOI
10.1016/j.fuel.2015.08.034
URI
https://scholarworks.unist.ac.kr/handle/201301/83260
Citation
FUEL, v.161, pp.1 - 11
Abstract
The general desulfurization process referred to as "indirect sulfation" takes place via a two-step process. Calcination makes limestone decompose to calcium oxide (CaO), and then SO2 molecules are adsorbed onto the calcined limestone. However, if the CO2 partial pressure in the system is higher than the equilibrium CO2 pressure over the limestone, an adsorption reaction between limestone and SO2 molecules can take place directly in the uncalcined state. This one-step process, called "direct sulfation," can apply to desulfurization in pressurized fluid-bed combustion (PFBC) or an oxy fuel combustion system capturing CO2. Limestone samples were reacted in a TGA apparatus, and the degrees of sulfation were measured under 100% air conditions for indirect sulfation and 80% CO2/20% O-2 conditions for direct sulfation to compare the mechanisms and kinetics of the two sulfation processes. SEM images of sulfated particles and EDS analyses showed that the gas diffusion of indirect sulfation takes place readily through macro-pores between the grains at a low conversion rate, and SO2 adsorption occurs over the interior of the limestone particles, whereas SO2 adsorption in direct sulfation takes place at the reaction interface, and the product (CaSO4) layer permeates into the interior from the surface of the limestone particles as direct sulfation proceeds. Thus, the grain model and the shrinking unreacted core model are applicable to describing the kinetics of indirect and direct sulfation, respectively. These model predictions agreed with experimental data, and the kinetic parameters obtained from experiments are consistent with the mechanisms. Furthermore, the high activation energy of the diffusion of direct sulfation and indirect sulfation with high conversion indicate that the diffusion mechanisms in the particles in direct sulfation and indirect sulfation at high conversion are both gas diffusion in pores and solid-state diffusion. These results may contribute to understanding why the characteristics of direct sulfation differ from those of indirect sulfation under certain conditions. (C) 2015 Elsevier Ltd. All rights reserved.
Publisher
ELSEVIER SCI LTD
ISSN
0016-2361
Keyword (Author)
Direct sulfationIndirect sulfationLimestoneCalcium carbonateMechanismDiffusion
Keyword
CALCIUM-BASED SORBENTSPRESSURECALCINATIONKINETICSRANGE

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