Thermochemical energy storage with the solid-gas reaction of SrCO3 improved with CaCO3

被引:0
作者
Padilla, Adriana Santamaria [1 ]
Romero-Paredes Rubio, Hernando [2 ]
Peralta, Rosalba Carrera [1 ]
Zamudio, Ruben Alfredo Hernandez [1 ]
机构
[1] Univ Autonoma Metropolitana, Posgrad Energia & Medio Ambiente, Ave Ferrocarril San Rafael Atlixco 186,Colonia Ley, Mexico City 09310, Mexico
[2] Univ Autonoma Metropolitana Iztapalapa, Dept Ingn Proc & Hidraul, Ave Ferrocarril San Rafael Atlixco 186,Colonia Ley, Mexico City 09310, Mexico
关键词
thermochemical energy storage; concentrating solar power; calcium carbonate; strontium carbonate; effective conversion; kinetics; CONCENTRATED SOLAR POWER; TEMPERATURE; INTEGRATION; SYSTEMS;
D O I
10.1515/ijcre-2024-0112
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In the context of thermochemical energy storage (TCES) for concentrating solar power (CSP) applications, metal carbonates' reversible calcination and carbonation are gaining prominence, particularly in the SrCO3/SrO system. This system is notable for its high theoretical energy density of 10.61 GJ/m(3) and operational temperatures up to 1,200 degrees C. However, like the CaCO3/CaO system, SrO experiences a significant drop in reactivity during cycling due to sintering and agglomeration of particles. In this work is proposed that the conversion effective will be improved by mixing the strontium carbonate with calcium carbonate. The best mix found was 80/20 SrCO3/CaCO3 with the operating parameters of calcination-carbonation temperatures of 1,200 degrees C and 900 degrees C, respectively. This reaction has a notably better stable conversion rate than pure strontium carbonate. The study was carried out using thermogravimetry analysis. The mixture was subjected to 9 cycles, and for the ninth cycle, there was an effective conversion of 33.14 %, which, compared to pure SrCO3, was 2.33 %; that was improved noticeably during the carbonation process. There was an increase in the percentage effective conversion of 30.81 %. Volumetric energy density was reduced from 6.93 to 2.81 GJ/m3 in the first and after nine cycles. The XRD analysis of the unprocessed mixture after 4 and 9 cycles showed no formation of new or secondary compounds, only the expected compounds: SrO, SrCO3, CaO, and CaCO3. This important change is explained during the carbonation looping because the CaO remains encapsulated in the SrCO3 and does not react completely at 900 degrees C. As a hypothesis, this encapsulation delays the sintering of the SrCO3. Using a Tcarb = 850 degrees C promotes the carbonation of CaO. By promoting CaO to react, the CaO encapsulated is released rapidly, and the material was sintering faster than the Tcarb = 900 degrees C. Comparing the seventh cycle at a Tcarb = 900 and 850 degrees C, it is observed that the effective conversion decreases from 0.4431 to 0.4202 and, in the same proportion, the volumetric energy density.
引用
收藏
页码:1301 / 1317
页数:17
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