吸附
阳离子聚合
热稳定性
单层
弗伦德利希方程
化学
甲基橙
打赌理论
朗缪尔
解吸
动力学
橙色G
无机化学
酸性染料
核化学
化学工程
高分子化学
有机化学
光催化
催化作用
工程类
生物化学
物理
量子力学
染色
作者
Kamyar Mirzaei,Erfan Jafarpour,Akbar Shojaei,Samaneh Salkhi Khasraghi,Peyman Jafarpour
标识
DOI:10.1016/j.apsusc.2023.156531
摘要
Stability of UiO-66 in 1 M HCl for different exposure times up to 15 days was investigated by employing various characterization techniques such as XRD, FESEM, TEM, TGA, and nitrogen adsorption/desorption. The lower surface area, smaller pore size, and slightly lower thermal stability indicated that the UiO-66 structure experienced a partial breakdown, but could maintain its main structure and showed acceptable stability. In addition, the exposure to the HCl solution added to the missing-linker defects in the structure of UiO-66. The adsorptive performance of HCl-aged UiO-66 nanoparticles towards anionic methyl orange (MO) dye was then evaluated. Compared to as-synthesized UiO-66, maximum dye adsorption capacity of HCl-aged UiO-66 towards MO exhibited over 60 % loss for 15 days aged UiO-66. Moreover, negative charges took over the positive surface charge of as-synthesized UiO-66 upon HCl aging. Therefore, the selective adsorption analysis showed that while neat UiO-66 adsorbs MO selectively over cationic dyes, acid-aged samples have a higher affinity towards cationic dyes. The adsorption kinetics of pristine and acid-aged UiO-66 particles were well outlined by pseudo-second-order, and isotherm studies demonstrated that the adsorption could be delineated well by the Langmuir and Freundlich model, inferring that adsorption takes place both multilayer and monolayer in parts.
科研通智能强力驱动
Strongly Powered by AbleSci AI