期刊
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 47, 期 23, 页码 9537-9543出版社
AMER CHEMICAL SOC
DOI: 10.1021/ie800882d
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This Study focuses oil the effect of various parameters of the synthesis procedure of the CO2 sorbent-CaO-Ca12Al14O33 derived from calcium acetate-on the CO2 sorption ability and lifetime. The synthesis procedure consists of the calcination of the acetate CaO precursor (step 1), the precipitation of the CaO with aluminum nitrates (step 2), followed by calcination at 500 degrees C for nitrates removal (step 3) and the calcination at 900 degrees C for the synthesis of Ca12Al14O33 (step 4). It has been shown, by employing TGA, that the applied difference in the calcination conditions (900 degrees C/2 h, 850 degrees C/1 h, 750 degrees C/0.5 h,) for the decomposition of the CaO acetate precursor (step I) is not adequate to affect the sorption fixation and stability results. On the other hand calcination history of the precipitate and the addition of water in between the two calcination steps (nitrates removal and Ca12Al14O33 synthesis reaction) are of high importance for ensuring sorption capacities higher than 6.5 mol CO2/kg of sorbent in the first cycle. SEM observations showed that the addition of water after calcination at 500 degrees C (step 3) accounts for the generation of the regular hexagonal crystalloids of Ca(OH)(2) which transforms in a porous network during calcination at 900 degrees C. It was also demonstrated that the quantity Of CO2 Molecules retained increases with decreasing aging time of the precipitate as a result of higher surface area (smaller crystal size) of the as-synthesized samples. The sorbent with the lower binder content (CaO/Ca12Al14O33 = 85:15) showed the prospective higher capacity (45% weight increase) in the first cycle but also a fair stability on repetitive sorption-desorption cycles.
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