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Abstract: The destruction of a chlorinated aromatic compound by UV photolysis and advanced oxidation was examined for potential use in air emissions treatment. The fluence rate distribution in a photoreactor was analyzed by a finite model, and this was used to estimate quantum yield and photonic efficiency for the photochemical decomposition of chlorobenzene in air. The analysis indicates that the quantum yield was constant at approximately 115%, but the presence of the common flue gas components sulfur dioxide and water could increase it to approximately 145%. Ozone, which strongly absorbs UV photons and promotes radical chain reactions, enhanced the quantum yield to 1534% when present at 2253ppm. When SO2 or ozone are present, “effective” quantum yield may be more informative for analysis, since it includes the number of photons absorbed by all reacting species. In this work, the effective QY ranged from 3.9% to 108.7%, with low values indicating that photons were wasted in processes that did not degrade the target organic. An analysis of photonic efficiency shows that the photo-reactor is more efficient at high concentrations of the target organic pollutant, and when ozone or sulfur dioxide are present. [Copyright &y& Elsevier]

The influence of humidity on the decomposition of gas phase chlorobenzene (CB) was studied in a batch photocatalytic reactor using TiO2 (anatase). Increasing relative humidity (>7% at 25°C and 1atm) resulted in an increasingly detrimental effect on the adsorption and photocatalytic decomposition rate of CB. Mechanistic analysis indicates that the relative hydrophilic/hydrophobic nature of a given chemical should dictate adsorption onto or penetration through water to the TiO2 surface. It is suggested that multiple layers of water molecules are formed at the TiO2 interface with air, even at low relative humidities. The multiple-layered film of water retards/prevents CB from reaching the reactive TiO2 surface or contacting radical species in the boundary layer. [Copyright &y& Elsevier]

Wet scrubbing of NOx was accomplished by hexamminecobalt(II) solution in a laboratory setting, and the spent absorbent was regenerated by thermal decomposition and acid treatment. The spent absorbent contained precipitates (cobalt nitrosyl) and soluble cobalt in the solution. Thermogravimetric analysis (TGA) showed that the spent sorbent could be decomposed to CoO at temperatures above 900 °C. Caution needed to be exercised to ensure that the samples were not exposed to oxygen when cooling down to ambient temperature in order to prevent oxidation of CoO to Co 3 O 4 . The regenerated cobalt(II) oxide was dissolved in HCl for preparation of hexamminecobalt(II) solutions, and such a regenerated cobalt-based sorbent for NO removal performed at the same level as the fresh one. This study suggests a practical method for the regeneration of a cobalt-based absorbent involved in NO absorption. [ABSTRACT FROM AUTHOR]