scholarly journals Catalytic Hydrodechlorination of Chlorophenols in a Continuous Flow Pd/CNT-Ni Foam Micro Reactor Using Formic Acid as a Hydrogen Source

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 77 ◽  
Author(s):  
Jun Xiong ◽  
Ying Ma

Catalytic hydrodechlorination (HDC) has been considered as a promising method for the treatment of wastewater containing chlorinated organic pollutants. A continuous flow Pd/carbon nanotube (CNT)-Ni foam micro reactor system was first developed for the rapid and highly efficient HDC with formic acid (FA) as a hydrogen source. This micro reactor system, exhibiting a higher catalytic activity of HDC than the conventional packed bed reactor, reduced the residence time and formic acid consumption significantly. The desired outcomes (dichlorination >99.9%, 4-chlorophenol outlet concentration <0.1 mg/L) can be obtained under a very low FA/substrate molar ratio (5:1) and short reaction cycle (3 min). Field emission scanning electron microcopy (FESEM) and deactivation experiment results indicated that the accumulation of phenol (the main product during the HDC of chlorophenols) on the Pd catalyst surface can be the main factor for the long-term deactivation of the Pd/CNT-Ni foam micro reactor. The catalytic activity deactivation of the micro reactor could be almost completely regenerated by the efficient removal of the absorbed phenol from the Pd catalyst surface.

Author(s):  
Victoria Skelton ◽  
Gillian Greenway ◽  
Stephen Haswell ◽  
Peter Styring ◽  
David Morgan ◽  
...  

2011 ◽  
Vol 248 (11) ◽  
pp. 2516-2519 ◽  
Author(s):  
Marta Mazurkiewicz ◽  
Artur Malolepszy ◽  
Anna Mikolajczuk ◽  
Leszek Stobinski ◽  
Andrzej Borodzinski ◽  
...  

Energies ◽  
2019 ◽  
Vol 12 (21) ◽  
pp. 4198 ◽  
Author(s):  
Vladimir Sobolev ◽  
Igor Asanov ◽  
Konstantin Koltunov

Formic acid (FA) can easily be decomposed, affording molecular hydrogen through a controllable catalytic process, thus attaining great importance as a convenient hydrogen carrier for hydrogen energetics. Supported gold nanoparticles are considered to be among the most promising catalysts for such applications. However, questions remain regarding the influence of the catalyst support on the reaction selectivity. In this study, we have examined the catalytic activity of typical gold catalysts, such as Au/TiO2, Au/SiO2, and Au/Al2O3 in decomposition of FA, and then compared it with the catalytic activity of corresponding supports. The performance of each catalyst and support was evaluated using a gas-flow packed-bed reactor. It is shown that the target reaction, FA → H2 + CO2, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA → H2O + CO, results exclusively from the acid-base behavior of supports.


2010 ◽  
Vol 12 (6) ◽  
pp. 843-846 ◽  
Author(s):  
Chunyu Du ◽  
Meng Chen ◽  
Wengang Wang ◽  
Geping Yin ◽  
Pengfei Shi

2021 ◽  
Vol 23 (5) ◽  
pp. 1978-1982
Author(s):  
Zhaofu Zhang ◽  
Shuaishuai Liu ◽  
Minqiang Hou ◽  
Guangying Yang ◽  
Buxing Han

Continuous-flow formic acid production from the hydrogenation of CO2 without any base, and the concentration of formic acid by electrodialysis was tested both offline and online.


2016 ◽  
Vol 6 (3) ◽  
pp. 869-874 ◽  
Author(s):  
Shu-Tao Gao ◽  
Weihua Liu ◽  
Cheng Feng ◽  
Ning-Zhao Shang ◽  
Chun Wang

Ag–Pd alloys deposited on an amine-functionalized UiO-66(NH2–UiO-66) have been successfully prepared via a pre-coordination method and used as a AgPd@NH2–UiO-66 catalyst with 100% H2 selectivity and a high catalytic activity.


Sign in / Sign up

Export Citation Format

Share Document