沸石
煅烧
吸附
吸附剂
重量分析
化学工程
傅里叶变换红外光谱
离子交换
化学
结构精修
无机化学
材料科学
离子
催化作用
有机化学
晶体结构
工程类
作者
Xinyu Sun,Quanqi Zhang,Sihan Li,Yiming Zhang,Meiyu Liu,Binbin He,Yi Mei,Yun Zu
标识
DOI:10.1016/j.cej.2024.148661
摘要
Ca-FAU zeolite sorbents have been recognized as one of promising CO2 capture materials, while it is subject to the change in the speciations and locations of Ca2+ species as adsorption sites in the FAU zeolite due to its susceptible migration. In this paper, a facile strategy is reported by tuning calcination temperatures and Ca loadings, to maximize the utilization of Ca2+ species in the supercages of CaNaX zeolites. Detail characterizations of TG-MS, in situ FTIR spectroscopy and XRD Rietveld refinement reveal the changeable regular in the chemical speciations, locations and number of Ca2+ species in the CaNaX zeolites. Synthetic 0.05CaNaX-250 zeolite (calcined at 250 °C and Ca loading of 1.58 wt%) guarantees at least 21 Ca(OH)+ species (depicted as hydroxylated Ca2+ species) in the supercages per FAU cell unit, close to theoretical value. Such sorbent apparently improves the CO2 uptakes and the separation from CO2/N2 and CO2/CH4, along with fast kinetics, low heat of adsorption, measured by dynamic and gravimetric adsorption methods, respectively. In addition, it keeps a superior recyclability after 10 times regeneration. CO2-dosing FTIR experiments further illustrate that excellent CO2 adsorption performance are benefited from the formation of Ca(OH)+∙∙∙(CO2)2 adducts with an appropriate interaction. This work is of great significance to better understand the role of cations in FAU zeolites, and also provides an important reference value for the directional design of effective adsorption sites in other excellent CO2 zeolite sorbents.
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