Title of article :
High-Pressure CO2 Adsorption onto NaX Zeolite: Effect of Li^+ , K^+ , Mg^2+, and Zn^2+ and Equilibrium Isotherms Study
Author/Authors :
Zouaoui ، El Hadi Materials Technology Laboratory - Houari Boumediene University of Science and Technology (USTHB) , Djamel ، Nibou Materials Technology Laboratory - Houari Boumediene University of Science and Technology (USTHB) , Wan Ab Karim Ghani ، Wan Azlina department of Chemical Environmental Engineering - Sustainable and Process Engineering Research Centre (SPERC) , Faculty of Engineering - University Putra Malaysia , Samira ، Amokrane Materials Technology Laboratory - Houari Boumediene University of Science and Technology (USTHB)
From page :
1195
To page :
1215
Abstract :
Due to the adverse effects of Carbon dioxide (CO2) emissions on the environment; various mitigation is regulated to control its emissions. In this study, CO2 adsorption isotherms on NaX or Faujasite X and exchanged zeolites with Li^+ (LiX), Zn ^+ (ZnX), Mg^2+ (MgX) and K^+ (KX) at different temperatures (298, 308, 323, 353, and 362 K) were investigated, using high pressure (3 MPa (30 bar)) thermogravimetric analyzer. The experimental results were then validated using numerous isotherm kinetics models namely Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Elovich, Toth, and Sips. From the study, it was found that the CO2 adsorption isotherms are characterized by a strong increase in low-pressure adsorption and a trend towards a high-pressure limit value Qmax. Specific surface area and pore volume revealed the most significant influent parameters for this study. These findings revealed that both experimental and modeling well correlated with Toth and Sips, gave the best results regardless of the material used.
Keywords :
NaX zeolite , Exchange cations , LiX, KX, MgX and ZnX , CO2 adsorption , Isotherme study
Journal title :
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Journal title :
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Record number :
2686664
Link To Document :
بازگشت