Extractive desulfurization of model fuel oil using ester functionalized imidazolium ionic liquids

2018 ◽  
Vol 196 ◽  
pp. 115-123 ◽  
Author(s):  
Jaganathan Joshua Raj ◽  
Sivapragasam Magaret ◽  
Matheswaran Pranesh ◽  
Kallidanthiyil Chellappan Lethesh ◽  
Wilfred Cecilia Devi ◽  
...  
2019 ◽  
Vol 213 ◽  
pp. 989-998 ◽  
Author(s):  
Jaganathan Joshua Raj ◽  
Sivapragasam Magaret ◽  
Matheswaran Pranesh ◽  
Kallidanthiyil Chellappan Lethesh ◽  
Wilfred Cecilia Devi ◽  
...  

Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1050
Author(s):  
Sarrthesvaarni Rajasuriyan ◽  
Hayyiratul Fatimah Mohd Zaid ◽  
Mohd Faridzuan Majid ◽  
Raihan Mahirah Ramli ◽  
Khairulazhar Jumbri ◽  
...  

The biggest challenge faced in oil refineries is the removal of sulfur compounds in fuel oil. The sulfur compounds which are found in fuel oil such as gasoline and diesel, react with oxygen in the atmosphere to produce sulfur oxide (SOx) gases when combusted. These sulfur compounds produced from the reaction with oxygen in the atmosphere may result in various health problems and environmental effects. Hydrodesulfurization (HDS) is the conventional process used to remove sulfur compounds from fuel oil. However, the high operating conditions required for this process and its inefficiency in removing the organosulfur compounds turn to be the major drawbacks of this system. Researchers have also studied several alternatives to remove sulfur from fuel oil. The use of ionic liquids (ILs) has also drawn the interest of researchers to incorporate them in the desulfurization process. The environmental effects resulting from the use of these ILs can be eliminated using eutectic-based ionic liquids (EILs), which are known as greener solvents. In this research, a combination of extractive desulfurization (EDS) and oxidative desulfurization (ODS) using a photocatalyst and EIL was studied. The photocatalyst used is a pre-reported catalyst, Cu-Fe/TiO2 and the EIL were synthesized by mixing choline chloride (ChCl) with organic acids. The acids used for the EILs were propionic acid (PA) and p-toluenesulfonic acid (TSA). The EILs synthesized were characterized using thermogravimetry analyser (TGA) differential scanning calorimetry (DSC) analysis to determine the physical properties of the EILs. Based on the TGA analysis, ChCl (1): PA (3) obtained the highest thermal stability whereas, as for the DSC analysis, all synthesized EILs have a lower melting point than its pure component. Further evaluation on the best EIL for the desulfurization process was carried out in a photo-reactor under UV light in the presence of Cu-Fe/TiO2 photocatalyst and hydrogen peroxide (H2O2). Once the oxidation and extraction process were completed, the oil phase of the mixture was analyzed using high performance liquid chromatography (HPLC) to measure the sulfur removal efficiency. In terms of the desulfurization efficiency, the EIL of ChCl (1): TSA (2) showed a removal efficiency of about 99.07%.


2021 ◽  
Vol 105 ◽  
pp. 103210
Author(s):  
Mariusz Zalewski ◽  
Tomasz Krawczyk ◽  
Agnieszka Siewniak ◽  
Aleksander Sobolewski

2021 ◽  
Vol 412 ◽  
pp. 128624
Author(s):  
Tian-Lin Ren ◽  
Xi-Wen Ma ◽  
Xiao-Qiong Wu ◽  
Li Yuan ◽  
Yang-Li Lai ◽  
...  

2021 ◽  
Vol 341 ◽  
pp. 130029
Author(s):  
Wenyan Yin ◽  
Khaled Tawfik Alali ◽  
Milin Zhang ◽  
Jingyuan Liu ◽  
Dalei Song ◽  
...  

Author(s):  
Justyna Łuczak ◽  
Jan Hupka ◽  
Jorg Thöming ◽  
Christian Jungnickel

2015 ◽  
Vol 11 ◽  
pp. 1641-1648 ◽  
Author(s):  
A Srinivas Reddy ◽  
Kenneth K Laali

Reaction of benzyl and ethyl allenoates with TMSX (X = I, Br, Cl) and with NH4SCN were investigated in MeCN, DMF, and in imidazolium ionic liquids [BMIM][NTf2] and [BMIM][PF6] as solvent, in the presence and absence of Selectfluor. Comparative product analysis studies demonstrate that the ability of Selectflour to promote oxidative/electrophilic dihalogenation/dithiocyanation with TMSX/NH4SCN (as observed previously for 1-arylallenes) is diminished in allenoates, most significantly in reactions with TMSCl, and essentially disappearing in reactions with NH4SCN, in favor of nucleophilic/conjugate addition. The study underscores the contrasting reactivity patterns in 1-arylallenes and allenoates toward electrophilic and nucleophilic additions in halofunctionalization with TMSX/Selectfluor and thiocyanation reactions with NH4SCN/Selectfluor. These competing pathways are influenced by the nature of the anion, allene structure, and the choice of solvent.


Sign in / Sign up

Export Citation Format

Share Document