Title of article :
Enhancement of the CO2 retention capacity of X zeolites by Na- and Cs-treatments Original Research Article
Author/Authors :
Eva D?az، نويسنده , , Emilio Mu?oz، نويسنده , , Aurelio Vega، نويسنده , , Salvador Ord??ez، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
8
From page :
1375
To page :
1382
Abstract :
Adsorption of carbon dioxide on alkaline modified X zeolites was investigated by temperature programmed desorption (TPD) analysis of these materials previously saturated with CO2 at 50, 100 and 200 °C. Parent X zeolite (in its sodium form) was treated with different sodium and cesium aqueous solutions, using both carbonates and hydroxides as precursors. The resulting materials were characterised by nitrogen physisorption, XRD, and NH3-TPD, in order to determine their morphological, crystallographic and chemical properties. Slight desilication phenomena were observed using hydroxides as precursors, whereas the treatment with Cs salts lead to higher crystallinity losses. Several successive adsorption–desorption cycles were carried out in order to check the regenerability of the adsorbents. Cesium-treated zeolites present higher carbon dioxide retention capacities than the sodium treated and than the parent material. When working with these Cs-modified materials, the desorption takes place mainly at temperatures between 250 and 400 °C, results of great practical interest, since it allows the use these kinds of materials for adsorption–desorption cycles. The evolution of the retention capacity with temperature is also markedly more positive for Cs-treated zeolite, especially when carbonate is used as the precursor. These materials maintain high retention capacities at 100 °C (10 mg g−1) and even at 200 °C (3 mg g−1), temperatures at which the most of the adsorbents are inactive.
Keywords :
CO2 Adsorption , CO2 sequestration , X-zeolites , Desilication , Cs-exchanged zeolites
Journal title :
Chemosphere
Serial Year :
2008
Journal title :
Chemosphere
Record number :
725763
Link To Document :
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