This paper presents the experimental investigations of the emissions of SO2, NO and N20 in a bench scale circulating fluidized bed combustor for coal combustion and co-firing coal and biomass. The thermal capacity of the combustor is 30 kW. The setup is electrically heated during startup. The infuence of the excess air, the degree of the air staging, the biomass share and the feeding position of the fuels on the emissions of SO2, NO and N2O were studied. The results showed that an increase in the biomass shares resulted in an increase of the CO concentration in the flue gas, probably due to the high volatile content of the biomass. In co-firing, the emission of SO2 increased with increasing biomass share slightly, however, non-linear increase relationship between SO2 emission and fuel sulfur content was observed. Air staging significantly decreased the NO emission without raising the SO2 level. Although the change of the fuel feeding position from riser to downer resulted in a decrease in the NO emission level, no obvious change was observed for the SO2 level. Taking the coal feeding position R as a reference, the relative NO emission could significantly decrease during co-firing coal and biomass when feeding fuel at position D and keeping the first stage stoichiometry greater than 0.95. The possible mechanisms of the sulfur and nitrogen chemistry at these conditions were discussed and the ways of simultaneous reduction of SO2, NO and N2O were proposed.
下行循环流化床反应器要求气固分离器具有分离效率高、气相停留时间短、压力损失小、设备磨损小等特点。利用气固二相在惯性上的差别,提出了一种新型同轴双锥两级气固快速分离器,并以FCC(F lu id Catalytic Crack ing)为循环物料对该型分离器的分离特性进行了研究。结果表明,同轴双锥两级气固分离器的分离效率在98%以上,气固分离器的压力损失在100 Pa以下,设备磨损小,能够满足下行循环流化床反应器的要求。
By using membrane dispersion micro-extractor, Ce（IIl） solvent extraction experiments were conducted. Cerium chloride solution with certain acidity was used as aqueous phase and 2-ethylhexyl phosphoric acid-2-ethylhexyl ester （EHEHPA） kerosene solution as organic phase. The effects of system physicochemical properties and operational conditions, such as initial EHEHPA concentration, initial aqueous acidity, total flow rate and continuous phase flow rate, etc., on the extraction efficiency and the overall volume mass transfer coefficient were evaluated. As the total flow rate increased fi＇om 20 to 160 mL/min, the overall volume mass transfer coefficient was enhanced from 0.1 to 0.54 S1. Under the optimal conditions, the Ce（III） extraction efficiency could reach 99.92% in 2.98 s. A mathematical model was set up to predict the overall volume mass transfer coefficient, and the calculation results agreed well with the experimental results, most relative error was within ＋10%.
