DFT-based study on the molecular interaction of hydrochloric acid with different extractants

被引:5
|
作者
Cao, Rui [1 ]
Tang, Panchun [1 ]
Yang, Xiaobo [2 ]
Sun, Ze [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Joint Int Lab Potassium & Lithium Strateg Resourc, Shanghai 200237, Peoples R China
[2] Qinghai Minzu Univ, Sch Chem & Chem Engn, Xining 810007, Peoples R China
基金
国家重点研发计划;
关键词
Solvent extraction; Density functional theory; Hydrochloric acid; ELECTRON-DENSITY ANALYSIS; HYDROGEN-BONDS; RECOVERY; COMPLEXATION; MODELS; METAL;
D O I
10.1016/j.molliq.2022.119108
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
As an important chemical raw material, hydrochloric acid widely exists in various chemical production processes. After being used in industrial production, an acidic waste solution will be produced, creating a need to recover hydrochloric acid from the waste solution. Solvent extraction is considered to be an efficient and easy-to-operate method. This paper uses DFT theory to study the binding characteristics of different kinds of extractants and hydrochloric acid molecules. The comprehensive analysis of RDG, AIM, and ELF found that hydrogen proton transfer occurs during hydrochloric acid extraction by amine extractants, and HCl is extracted by ionic association. At the same time, alcohols, ketones, esters, and neutral phosphorus-containing species are all bonded with HCl in the form of a hydrogen bond. In addition, by studying the changes of Gibbs free energy before and after the extraction process, it was found that amines had the most potent binding force to HCl. Moreover, the binding force of TEHA to HCl is much smaller than that of other amines, which not only retains the ability to extract HCl but also makes it have excellent stripping performance. Finally, the results of the DFT calculation are verified by experiments.(c) 2022 Elsevier B.V. All rights reserved.
引用
收藏
页数:12
相关论文
共 50 条
  • [1] DFT-based QSAR Study of Substituted Pyridine-Pyrazole Derivatives as Corrosion Inhibitors in Molar Hydrochloric Acid
    El Adnani, Z.
    Benjelloun, A. T.
    Benzakour, M.
    Mcharfi, M.
    Sfaira, M.
    Saffaj, T.
    Touhami, M. Ebn
    Hammouti, B.
    Al-Deyab, S. S.
    Ebenso, Eno E.
    INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE, 2014, 9 (09): : 4732 - 4746
  • [2] DFT-based QSAR study of valproic acid and its derivatives
    Hashemianzadeh, Majid
    Safarpour, Mohammad Ali
    Gholamjani-Moghaddam, Kiana
    Mehdipour, Ahmad Reza
    QSAR & COMBINATORIAL SCIENCE, 2008, 27 (04): : 469 - 474
  • [3] Hydration of methanol in water. A DFT-based molecular dynamics study
    van Erp, TS
    Meijer, EJ
    CHEMICAL PHYSICS LETTERS, 2001, 333 (3-4) : 290 - 296
  • [4] Phase Properties of Different HfO2 Polymorphs: A DFT-Based Study
    Laudadio, Emiliano
    Stipa, Pierluigi
    Pierantoni, Luca
    Mencarelli, Davide
    CRYSTALS, 2022, 12 (01)
  • [5] DFT-Based Molecular Transport Implementation in ADF/BAND
    Verzijl, C. J. O.
    Thijssen, J. M.
    JOURNAL OF PHYSICAL CHEMISTRY C, 2012, 116 (46): : 24393 - 24412
  • [6] A DFT-based mechanistic study on the formation of oximes
    Kirmizialtin, Serdal
    Yildiz, Banu Sizirici
    Yildiz, Ibrahim
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 2017, 30 (12)
  • [7] DFT-based QSAR study and molecular design of AHMA derivatives as potent anticancer agents
    Chen, Jincan
    Shen, Yong
    Liao, Siyan
    Chen, Lanmei
    Zheng, Kangcheng
    INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2007, 107 (06) : 1468 - 1478
  • [8] On the hydrolysis of iron ions: DFT-based molecular dynamics perspective
    Esmaeilbeig, M. A.
    Khorram, M.
    Ayatollahi, S.
    Zolghadr, A. R.
    JOURNAL OF MOLECULAR LIQUIDS, 2022, 367
  • [9] Acidity constants from DFT-based molecular dynamics simulations
    Sulpizi, Marialore
    Sprik, Michiel
    JOURNAL OF PHYSICS-CONDENSED MATTER, 2010, 22 (28)
  • [10] Self-interaction error in DFT-based modelling of ionic liquids
    Lage-Estebanez, Isabel
    Ruzanov, Anton
    Garcia de la Vega, Jose M.
    Fedorov, Maxim V.
    Ivanistsev, Vladislav B.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2016, 18 (03) : 2175 - 2182