A non-chemically selective top-down approach towards the preparation of hierarchical TS-1 zeolites with improved oxidative desulfurization catalytic performance

2016 ◽  
Vol 52 (17) ◽  
pp. 3580-3583 ◽  
Author(s):  
Shuting Du ◽  
Xiaoxin Chen ◽  
Qiming Sun ◽  
Ning Wang ◽  
Mingjun Jia ◽  
...  

Hierarchical TS-1 zeolites with enhanced performance in oxidative desulfurization of bulky molecules are prepared by treatment in fluoride medium.


2010 ◽  
Vol 148-149 ◽  
pp. 924-928
Author(s):  
Xue Min Yan ◽  
Yuan Zhu Mi

Two kinds of mesoporous HPW/SiO2 composites, which have been synthesized respectively by the amino-functionalized (AF) method and evaporation-induced self-assembly (EISA) method, have been used as catalysts in the oxidative desulfurization process of dibenzothiophene(DBT). The catalytic performance results show that the catalyst synthesized by EISA method holds higher catalytic activity than that synthesized by the AF method. The difference of catalytic activity can be attributed to the different synthesis mechanism of two kinds of composites. In the AF method, the bonding force between HPW and SiO2 is strong acid-base interaction, which damages the Keggin structure. Whereas in the EISA process, electrostatic force and hydrogen bonds between W=O groups and Si-OH groups are main bonding forces. The hydrogen bond holds the electron-withdrawing effect, which increases the activity of nonbonding W=O groups in HPW and then results in the enhancement of the catalytic activity.



Nanomaterials ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 955 ◽  
Author(s):  
Jing Liu ◽  
Jiao Yin ◽  
Bo Feng ◽  
Tao Xu ◽  
Fu Wang

The Pt particles within diameters of 1–3 nm known as Pt nanoclusters (NCs) are widely considered to be satisfactory oxygen reduction reaction (ORR) catalysts due to higher electrocatalytic performance and cost effectiveness. However, the utilization of such smaller Pt NCs is always limited by the synthesis strategies, stability and methanol tolerance of Pt. Herein, unprotected Pt NCs (~2.2 nm) dispersed on carbon nanotubes (CNTs) were prepared via a modified top-down approach using liquid Li as a solvent to break down the bulk Pt. Compared with the commercial Pt/C, the resultant Pt NCs/CNTs catalyst (Pt loading: 10 wt.%) exhibited more desirable ORR catalytic performance in 0.1 M HClO4. The specific activity (SA) and mass activity (MA) at 0.9 V for ORR over Pt NCs/CNTs were 2.5 and 3.2 times higher than those over the commercial Pt/C (Pt loading: 20 wt.%). Meanwhile, the Pt NCs/CNTs catalyst demonstrated more satisfactory stability and methanol tolerance. Compared with the obvious loss (~69%) of commercial Pt/C, only a slight current decrease (~10%) was observed for Pt NCs/CNTs after the chronoamperometric measurement for 2 × 104 s. Hence, the as-prepared Pt NCs/CNTs material displays great potential as a practical ORR catalyst.





2019 ◽  
Vol 22 (4) ◽  
pp. 321-326 ◽  
Author(s):  
Xiaolin Li ◽  
Hui Qi ◽  
Wei Zhou ◽  
Wei Xu ◽  
Yinyong Sun


2014 ◽  
Vol 636 ◽  
pp. 93-96
Author(s):  
Ming Zhang ◽  
Wen Shuai Zhu ◽  
Meng Li ◽  
Yan An Li ◽  
Suhang Xun ◽  
...  

Tungsten-containing functional mesoporousW-SiO2 have been successfully synthesized by an one-pot and facile room-temperature procedure. These materials presented a high dispersion of tungsten species and excellent catalytic activity on the removal of sulfur compounds without any organic solvents as extractants. The catalytic performance on sulfur compounds was investigated in detail. After recycling for 8 times, the removal of the oxidation desulfurization system could still reach 92.0%.





Fuel ◽  
2015 ◽  
Vol 147 ◽  
pp. 195-202 ◽  
Author(s):  
Jianghua Qiu ◽  
Guanghui Wang ◽  
Yuqin Zhang ◽  
Danlin Zeng ◽  
Yang Chen


RSC Advances ◽  
2017 ◽  
Vol 7 (85) ◽  
pp. 54266-54276 ◽  
Author(s):  
Haiyan Ji ◽  
Haitao Ju ◽  
Rong Lan ◽  
Peiwen Wu ◽  
Jia Sun ◽  
...  

An ionic liquid modified hexagonal boron nitride was developed for preparation of a supported catalyst with enhanced stability and excellent catalytic performance in catalytic oxidative desulfurization.







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