Facile Construction of Magnetic Ionic Liquid Supported Silica for Aerobic Oxidative Desulfurization in Fuel

With the rapid growth in fuel demand, deep desulfurization of fuel oil is vitally necessary for the sake of health and environmental protection. In this work, a kind of magnetic ionic liquid supported silica is prepared by a facile ball milling method, and applied in the aerobic oxidative desulfurization of organosulfurs in fuel. The experimental results indicated that ball milling procedure can increase the specific surface area of samples, which is beneficial to oxidative desulfurization process. Under the optimal reaction conditions, the prepared materials can have an entire removal of aromatic sulfur compounds as well as a good recycling ability. Moreover, the introduction of Fe3O4 did not decline the desulfurization performance, but help the catalyst to be easily separated after reaction.

Immobilization of K7PW11O39 on ZrO2 Nanofiber: Ultra-deep Desulfurization Based in Extraction Catalytic Oxidation Desulfurization System

In this work, K7PW11O39 (abbreviated as PW11) was immobilized on ZrO2 nanofibers and used as an efficient recyclable catalyst in extraction catalytic oxidation desulfurization system (ECODS).The 500 ppm DBT model oil(5mL) can desulphurize completely within 20 min with the catalytic conditions of 50��, 0.010 g 50 wt%- CTAB�C PW11�CZrO2 nanofibers and O/S molar ratio H2O2/DBT molar ratio�� was 2:1. The synthesized catalyst was characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and thermo gravimetric analyzer (TGA). The results indicated the PW11�CZrO2 nanofibers were synthesized successfully and the possible catalytic mechanism is also revealed.

Aluminum-Free Steelmaking: Desulfurization and Nonmetallic Inclusion Evolution of Si-Killed Steel in Contact with CaO-SiO2-CaF2-MgO Slag

In some applications, deep desulfurization and deoxidation of steels without the use of aluminum are required, using Si as a deoxidant instead, with double-saturated slags in the CaO-SiO2-CaF2-MgO system. This work studied the desulfurization and nonmetallic inclusion evolution for the system using an induction furnace and compared the results with FactSage kinetic simulations. Steel samples were taken from the steel melt and analyzed with ICP-MS and combustion analysis for chemistry, and SEM/EDS for nonmetallic inclusion quantity, size, and composition. The results indicate that the steel was deeply desulfurized, with a final sulfur partition coefficient of 580; MgO was reduced from the slag, yielding dissolved [Mg] that transformed liquid Mn–silicate inclusions into forsterite and MgO. Intentional reoxidation of the melt with oxidized electrolytic iron demonstrated a significant concentration of dissolved [Mg] in the steel, by the formation of additional forsterite and MgO upon reoxidation.