吸附
腐植酸
水溶液
吉布斯自由能
化学
焓
标准摩尔熵
朗缪尔
化学吸附
热力学
标准生成焓
物理化学
有机化学
物理
肥料
作者
Fande Meng,Qiuxiang Huang,Steven L. Larson,Fengxiang X. Han
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-10-18
卷期号:37 (43): 12557-12567
被引量:15
标识
DOI:10.1021/acs.langmuir.1c01838
摘要
The humic substance is a low-cost and effective adsorbent with abundant functional groups in remediating uranium (U) (VI)-contaminated water. In this research study, leonardite together with leonardite-derived humic acid (L-HA) was used to eliminate U(VI) from water under diverse temperatures (298, 308, and 318 K). L-HA showed a higher adsorption volume for U(VI) than leonardite. U adsorption was varied with pH and increased with temperature. The adsorption kinetics of L-HA had a higher determination coefficient (R2) for pseudo-second-order (R2 > 0.993) and Elovich (R2 > 0.987) models, indicating possible chemisorption-assisted adsorption. This was further supported with the activation energies (15.9 and 13.2 kJ/mol for leonardite and L-HA, respectively). Moreover, U(VI) equilibrium adsorption on leonardite was better depicted with the Freundlich model (R2 > 0.970), suggesting heterogeneous U(VI) adsorption onto the leonardite surface. However, U(VI) adsorption onto L-HA followed the Langmuir equation (R2 > 0.971), which implied the dominant role of monolayer adsorption in controlling the adsorption process. Thermodynamic parameters, including standard entropy change (ΔS0 > 0), Gibbs free energy (ΔG0 < 0), and standard enthalpy change (ΔH0 > 0), suggested a spontaneous and endothermal adsorption process. In addition, ionic species negatively affected U(VI) adsorption by leonardite and L-HA.
科研通智能强力驱动
Strongly Powered by AbleSci AI