Synthesis of modified carbon nanotube-supported Pd and the catalytic performance for hydrodehalogenation of aryl halides

2013 ◽  
Vol 91 (5) ◽  
pp. 307-314 ◽  
Author(s):  
Yuandong Xu ◽  
Long Chen ◽  
Xiaolai Wang

The effects of surface functionalization on the deposition of Pd nanoparticles on multi-walled carbon nanotubes (CNTs) have been studied. Two methods were used for the functionalization of CNTs: one employed a 1:1 (v/v) mixture of concentrated H2SO4/HNO3, sonicated at RT; the other employed a 3:1 (v/v) mixture of concentrated H2SO4/HNO3, sonicated at 60 °C. A large number of surface oxide groups were introduced on the surface of functionalized CNTs, especially in strong oxidation power (H2SO4/HNO3 = 3:1, 60 °C). The dispersion of Pd nanoparticles on CNTs was found to depend on the amount of surface oxide groups, with larger amounts of surface oxide groups resulting in higher dispersion of Pd nanoparticles. The effects of CNT surface functionalization on the performance of Pd/CNTs catalysts were studied, and the reaction conditions optimized, using the hydrodebromination of bromobenzene as model reaction. Under optimal conditions, the hydrodehalogenation of various aryl halides were tested over Pd/CNTs catalysts.

2015 ◽  
Vol 5 (8) ◽  
pp. 4144-4153 ◽  
Author(s):  
Vijay M. Shinde ◽  
Emmanuel Skupien ◽  
Michiel Makkee

A simple approach to synthesize highly dispersed Pd nanoparticles on CNTs without a capping agent is presented which exhibits high activity and selectivity for selective oxidation of benzyl alcohol.


2020 ◽  
Vol 98 (2) ◽  
pp. 57-65 ◽  
Author(s):  
Wei Long ◽  
Pingle Liu ◽  
Wei Xiong ◽  
Fang Hao ◽  
He’an Luo

Acid-treated, multi-walled carbon nanotube (AMWCNT) supported Ru and MnO bimetallic catalysts were prepared for liquid phase hydrodeoxygenation of guaiacol. The physicochemical properties of the prepared catalysts were characterized by FTIR, XRD, NH3-TPD, CO2-TPD, TEM, and XPS. MnO species were loaded on the inner surface of carbon nanotubes and were helpful for Ru particle dispersion. The 6%Ru-8%MnO/AMWCNTs with smaller Ru particle size, better dispersion, and more basic sites gave the best catalytic performance of 99.38% conversion of guaiacol and 85.84% selectivity to cyclohexanol. The effects of reaction conditions on liquid phase guaiacol hydrodeoxygenation were discussed and a possible reaction path was proposed.


RSC Advances ◽  
2016 ◽  
Vol 6 (92) ◽  
pp. 88916-88924 ◽  
Author(s):  
Mahsa Hajighorbani ◽  
Malak Hekmati

The prepared Isoniazide-MWCNTs were used to deposition of Pd NPs as novel nanocatalyst. The catalyst showed high activity in Suzuki coupling reaction of aryl halides (X = I, Br, Cl).


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1728
Author(s):  
Latifah A. Alshabanah ◽  
Sobhi M. Gomha ◽  
Laila A. Al-Mutabagani ◽  
Tariq Z. Abolibda ◽  
Nahed A. Abd El-Ghany ◽  
...  

Aminohydrazide cross-linked chitosan (CLCS) and its MWCNTs (CLCS/MWCNTs) were formulated and utilized as a potent ecofriendly basic heterogeneous biocatalyst under ultrasonic irradiation for synthesis of two novel series of benzil bis-aryldiazenylthiazoles and benzil bis-arylhydrazonothiazolones from the reaction of benzil bis-thiosemicarbazone with 2-oxo-N′-arylpropanehydrazonoyl chlorides and ethyl 2-chloro-2-(2-phenylhydrazono) acetates, respectively. The chemical structures of the newly synthesized derivatives were elucidated by spectral data and alternative methods, where available. Additionally, their yield % was estimated using a traditional catalyst as TEA and green recyclable catalysts as CLCS and CLCS/MWCNTs composite in a comparative study. We observed that, under the same reaction conditions, the yield % of the desired products increased by changing TEA to CLCS then to CLCS/MWCNT from 72–78% to 79–83% to 84–87%, respectively. The thermal stability of the investigated samples could be arranged as CLCS/MWCNTs composite > CLCS > chitosan, where the weight losses of chitosan, CLCS and CLCS/MWCNTs composite at 500 °C were 65.46%, 57.95% and 53.29%, respectively.


2020 ◽  
Vol 41 (2) ◽  
pp. 357-363 ◽  
Author(s):  
Zhi-Feng Jiao ◽  
Ji-Xiao Zhao ◽  
Xiao-Ning Guo ◽  
Xiang-Yun Guo

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