04/00151 Effect of the precursor and the preparation method on copper based activated carbon catalysts for methanol decomposition to hydrogen and carbon monoxide

2004 ◽  
Vol 45 (1) ◽  
pp. 19
2003 ◽  
Vol 81 (10) ◽  
pp. 1096-1100 ◽  
Author(s):  
Tanya Tsoncheva ◽  
Radostin Nickolov ◽  
Svetoslava Vankova ◽  
Dimitar Mehandjiev

A comparison of the abilities of CuO – activated carbon catalysts, prepared by different copper precursors and preparation techniques, in the methanol decomposition reaction to carbon monoxide and hydrogen was undertaken. Higher catalytic activity and stability are found for the catalysts obtained from an ammonia solution of copper carbonate. The nature of the catalytic active complex in the samples is also discussed. Key words: methanol decomposition, CuO – activated carbon catalysts, catalytic active complex.


2005 ◽  
Vol 225 (2) ◽  
pp. 245-251 ◽  
Author(s):  
T. Tsoncheva ◽  
S. Vankova ◽  
O. Bozhkov ◽  
D. Mehandjiev

Processes ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 504
Author(s):  
Yane Ansanay ◽  
Praveen Kolar ◽  
Ratna Sharma-Shivappa ◽  
Jay Cheng ◽  
Consuelo Arellano

In the present research, activated carbon-supported sulfonic acid catalysts were synthesized and tested as pretreatment agents for the conversion of switchgrass into glucose. The catalysts were synthesized by reacting sulfuric acid, methanesulfonic acid, and p-toluenesulfonic acid with activated carbon. The characterization of catalysts suggested an increase in surface acidities, while surface area and pore volumes decreased because of sulfonation. Batch experiments were performed in 125 mL serum bottles to investigate the effects of temperature (30, 60, and 90 °C), reaction time (90 and 120 min) on the yields of glucose. Enzymatic hydrolysis of pretreated switchgrass using Ctec2 yielded up to 57.13% glucose. Durability tests indicated that sulfonic solid-impregnated carbon catalysts were able to maintain activity even after three cycles. From the results obtained, the solid acid catalysts appear to serve as effective pretreatment agents and can potentially reduce the use of conventional liquid acids and bases in biomass-into-biofuel production.


2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Nicolás Carrara ◽  
Carolina Betti ◽  
Fernando Coloma-Pascual ◽  
María Cristina Almansa ◽  
Laura Gutierrez ◽  
...  

A series of low-loaded metallic-activated carbon catalysts were evaluated during the selective hydrogenation of a medium-chain alkyne under mild conditions. The catalysts and support were characterized by ICP, hydrogen chemisorption, Raman spectroscopy, temperature-programmed desorption (TPD), temperature-programmed reduction (TPR), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR micro-ATR), transmission electronic microscopy (TEM), and X-ray photoelectronic spectroscopy (XPS). When studying the effect of the metallic phase, the catalysts were active and selective to the alkene synthesis. NiCl/C was the most active and selective catalytic system. Besides, when the precursor salt was evaluated, PdN/C was more active and selective than PdCl/C. Meanwhile, alkyne is present in the reaction media, and geometrical and electronic effects favor alkene desorption and so avoid their overhydrogenation to the alkane. Under mild conditions, nickel catalysts are considerably more active and selective than the Lindlar catalyst.


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