| Literature DB >> 28654786 |
Lingwan Hao1, Meiri Wang1, Wenjuan Shan2, Changliang Deng1, Wanzhong Ren1, Zhouzhou Shi1, Hongying Lü3.
Abstract
A series of L-proline-based DESs was prepared through an atom economic reaction between L-proline (L-Pro) and four different kinds of organic acids. The DESs were characterized by Fourier transform infrared spectroscopy (FT-IR), H nuclear magnetic resonance (1HNMR), cyclic voltammogram (CV) and the Hammett method. The synthesized DESs were used for the oxidative desulfurization and the L-Pro/p-toluenesultonic acid (L-Pro/p-TsOH) system shows the highest catalytic activity that the removal of dibenzothiophene (DBT) reached 99% at 60°C in 2h, which may involve the dual activation of the L-Pro/p-TsOH. The acidity of four different L-proline-based DESs was measured and the results show that it could not simply conclude that the correlation between the acidity of DESs and desulfurization capability was positive or negative. The electrochemical measurements evidences and recycling experiment indicate a good stability performance of L-Pro/p-TsOH in desulfurization. This work will provide a novel and potential method for the deep oxidation desulfurization.Entities:
Keywords: DBT; Diesel; L-proline-based DESs; Oxidative desulfurization
Year: 2017 PMID: 28654786 DOI: 10.1016/j.jhazmat.2017.06.050
Source DB: PubMed Journal: J Hazard Mater ISSN: 0304-3894 Impact factor: 10.588