Experiments of simultaneous removal of SO2 and NO from simulated flue gas, using NaClO2 solution as the absorbent, were carried out in a self-designed bubble reactor, and high simultaneous removal efficiencies
of SO2 and NO were obtained under the optimal experimental conditions. The mechanism of simultaneous removal based on NaClO2 acid solutions was proposed by analyzing the removal products. Possibility and limitation of the desulfurization and denitrification
using NaClO2 acid solutions were calculated by thermodynamic methods. Experimental results of reaction kinetics for simultaneous desulfurization
and denitrification indicated that the oxidation-absorption processes of SO2 and NO were divided into two zones, namely the fast and slow reaction zones. In the slow reaction zones both were zero order
reactions, and in the fast reaction zones, the reaction order, rate constant and activation energy of SO2 reaction with absorbent were 1.4, 1.22 (mol·L−1)−0.4·s−1 and 66.25 kJ·mol−1, respectively, and 2, 3.15×103 (mol·L−1) −1·s−1, and 42.50 kJ·mol−1 for NO reaction, respectively.
Supported by the National High-Tech Research and Development Program of China (“863” Project) (Grant No. 2007AA061803) 相似文献
A simplified mathematical model leading to a closed form of solution is developed for estimation of nitric oxide emission from a coal fired circulating fluidized bed (CFB) furnace. The furnace is divided into two sections: a lower section below and an upper section above the secondary air injection level. Reactions in the cyclone and the return leg are neglected. Furnace dimensions, coal feed rate, coal composition and furnace temperature are inputs to the model which was validated against several pilot scale and commercial units. Experimental results from two pilot plants and two commercial power plants agree with model predictions. A sensitivity analysis was carried out using the model to examine the effect of different operating parameters and coal properties on the overall NO emission from the furnace. It was found that excess air and furnace temperature are most important factors influencing the NO emission level. The primary to secondary air ratio influences the NO emission level reasonably. Properties of coal are other factors which affect the NO emission to a large extent. The model, though it invovles some simplification, predicts the overall emission of NO with a level of accuracy accepted in commercial operation. 相似文献
The role of La2O3 loading in Pd/Al2O3-La2O3 prepared by sol–gel on the catalytic properties in the NO reduction with H2 was studied. The catalysts were characterized by N2 physisorption, temperature-programmed reduction, differential thermal analysis, temperature-programmed oxidation and temperature-programmed desorption of NO.
The physicochemical properties of Pd catalysts as well as the catalytic activity and selectivity are modified by La2O3 inclusion. The selectivity depends on the NO/H2 molar ratio (GHSV = 72,000 h−1) and the extent of interaction between Pd and La2O3. At NO/H2 = 0.5, the catalysts show high N2 selectivity (60–75%) at temperatures lower than 250 °C. For NO/H2 = 1, the N2 selectivity is almost 100% mainly for high temperatures, and even in the presence of 10% H2O vapor. The high N2 selectivity indicates a high capability of the catalysts to dissociate NO upon adsorption. This property is attributed to the creation of new adsorption sites through the formation of a surface PdOx phase interacting with La2O3. The formation of this phase is favored by the spreading of PdO promoted by La2O3. DTA shows that the phase transformation takes place at temperatures of 280–350 °C, while TPO indicates that this phase transformation is related to the oxidation process of PdO: in the case of Pd/Al2O3 the O2 uptake is consistent with the oxidation of PdO to PdO2, and when La2O3 is present the O2 uptake exceeds that amount (1.5 times). La2O3 in Pd catalysts promotes also the oxidation of Pd and dissociative adsorption of NO mainly at low temperatures (<250 °C) favoring the formation of N2. 相似文献