Ti2C-MXene/activated carbon nanocomposite for efficient CO2 capture: Insights into thermodynamics properties

物理吸附 弗伦德利希方程 纳米复合材料 朗缪尔吸附模型 吸附 化学吸附 热力学 活性炭 朗缪尔 材料科学 化学 化学工程 纳米技术 有机化学 吸附 物理 工程类
作者
Mansur Aliyu,Basiru O. Yusuf,AbdulHakam Shafiu Abdullahi,Idris A. Bakare,Mustapha Umar,Abbas Saeed Hakeem,Saheed A. Ganiyu
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:340: 126737-126737 被引量:22
标识
DOI:10.1016/j.seppur.2024.126737
摘要

This study investigates the uniqueness and intrinsic properties of a composite material, composed of Ti2CTx MXene and activated carbon (AC), for efficient adsorption of CO2. The evaluation is carried out through a combination of experimental and computational methods at various process conditions. The Ti2C-MXene/AC nanocomposite materials are synthesized by solid-state impregnation (SSI), and their properties are characterized using techniques such as N2-sorption, Raman, FTIR, XRD, SEM, and TEM. The characterization results demonstrate that the MXene particles are evenly dispersed and maintain their crystalline structure on the AC surface for maximum adsorption of CO2. Analyzing the CO2 isotherm data reveals that incorporating MXene enhances the CO2 adsorption capacity of AC, with an optimal loading of 2.5 wt% MXene. The adsorption capacity of AC increased from 46.46 cm3/g to 67.83 cm3/g when 2.5 wt% of MXene was introduced. The experimental isotherm data are fitted to Freundlich, Langmuir, Sips, and Tóth, isotherm models. The parameters of these models are employed to determine the thermodynamic characteristics of the adsorption process. The goodness-of-fit of the CO2 isotherm models is found to be excellent, with R2 values consistently exceeding 0.99 in nearly all cases. Thermodynamic analysis indicates that the adsorption processes, favorable, spontaneous, and involve physisorption multiple layers adsorption, while kinetic modeling indicates the dominance of chemisorption in AC-MX-x based adsorbent. Furthermore, a selectivity analysis demonstrates that the adsorbent has a higher affinity for CO2.
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