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Capture of Gas-Phase Arsenic Oxide by Lime: Kinetic and Mechanistic Studies

2001; American Chemical Society; Volume: 35; Issue: 4 Linguagem: Inglês

10.1021/es001405m

1520-5851

Raja A. Jadhav, Liang‐Shih Fan,

Industrial Gas Emission Control

Trace metal emission from coal combustion is a major concern for coal-burning utilities. Toxic compounds such as arsenic species are difficult to control because of their high volatility. Mineral sorbents such as lime and hydrated lime have been shown to be effective in capturing arsenic from the gas phase over a wide temperature range. In this study, the mechanism of interaction between arsenic oxide (As2O3) and lime (CaO) is studied over the range of 300−1000 °C. The interaction between these two components is found to depend on the temperature; tricalcium orthoarsenate (Ca3As2O8) is found to be the product of the reaction below 600 °C, whereas dicalcium pyroarsenate (Ca2As2O7) is found to be the reaction product in the range of 700−900 °C. Maximum capture of arsenic oxide is found to occur in the range of 500−600 °C. At 500 °C, a high reactivity calcium carbonate is found to capture arsenic oxide by a combination of physical and chemical adsorption. Intrinsic kinetics of the reaction between calcium oxide and arsenic oxide in the medium-temperature range of 300−500 °C is studied in a differential bed flow-through reactor. Using the shrinking core model, the order of reaction with respect to arsenic oxide concentration is found to be about 1, and the activation energy is calculated to be 5.1 kcal/mol. The effect of initial surface area of CaO sorbent is studied over a range of 2.7−45 m2/g using the grain model. The effect of other major acidic flue gas species (SO2 and HCl) on arsenic capture is found to be minimal under the conditions of the experiment.