Exothermic Performance of the Calcined Limestone Determined by Exothermic Temperature under Fluidization during CaCO_(3)/CaO Energy Storage Cycles

Thermochemical energy storage based on CaO/CaCO_(3)cycles has obtained significant attention as an alternative energy storage solution for concentrated solar power plants.In view of the applicability of fluidized bed reactors for CaO/CaCO_(3)heat storage,it is imperative to study the factors related to the heat release performance of CaO.This work presents an exothermic experiment on calcined limestone under fluidization,exploring the impact of initial temperature,CO_(2)concentration,particle size,superficial gas velocity,and number of cycles on the exothermic performance of CaO.The result indicates that CaO with high initial temperature leads to higher exothermic temperature,with better exothermic stability under cycles.An optimal initial temperature range of 600℃-650℃exists with an actual CaO conversion rate deviating merely 2%from theoretical conversion.Higher CO_(2)concentration augments the exothermic temperature and rate of CaO,while also improves the effective conversion of CaO.Nevertheless,high CO_(2)concentrations exacerbate the sintering and deactivation of CaO.High superficial gas velocity and small particle size shorten the exothermic time by increasing heat dissipation,but has minimal effect on the exothermic properties.Finally,the exothermic properties of CaO under fluidized and static conditions are studied.The result shows that exothermic temperature and exothermic rate of CaO under fluidization are enhanced,displaying higher heat storage performance than that under static state.This study provides valuable insights for optimizing the exothermic performance of CaO in fluidized bed reactors,contributing to advanced thermochemical energy storage for concentrated solar power plants.

Study on electrochemical property of La_(0.75)Mg_(0.25)Ni_(2.85)Co_(0.45–x)(AlSn)_x (x=0.0,0.1,0.2,0.3) alloys

La_（0.75）Mg_（0.25）Ni_（2.85）Co_（0.45–x）（AlSn）_x（AlSn）_x（x=0.0,0.1,0.2,0.3） alloys were prepared by magnetic induction melting method, and the phase composition and electrochemical properties were investigated systematically. The alloys were mainly composed of LaNi5, La2Ni7 and LaNi3 phase, and the cell volume of LaNi5 increased with the Al and Sn contents. For the alloy corresponding to x=0.0, the Cmax and C150 were 348.9 and 185 mA h/g, respectively, then for the alloy electrode with x=0.2, even though the Cmax was only 309.0 mA h/g less than 348.9 mA h/g, the C150 of 231 mA h/g was much higher than 185 mA h/g. And the values of the limit current density, anodic peak current density and hydrogen diffusion coefficient of the La0.75Mg0.25Ni2.85Co0.35（AlS n）0.1（x=0.1） alloy were 1079.5, 1023.8 mA /g and 5.71×10–10 cm2/s, respectively. Which were the highest than that of any other electrodes. These results suggested that the kinetic property of the La_（0.75）Mg_（0.25）Ni_（2.85）Co_（0.45–x）（AlSn）_x（AlSn）_x（x=0.0, 0.1, 0.2, 0.3） electrodes could be improved effectively by adding moderate contents of Al and Sn.