Kinetic study of the drying step of supported catalysts by reversed-flow gas chromatography

1982 ◽  
Vol 15 (6) ◽  
pp. 351-354 ◽  
Author(s):  
G. Karaiskakis ◽  
A. Lycourghiotis ◽  
N. A. Katsanos
1992 ◽  
Vol 27 (15) ◽  
pp. 2055-2070 ◽  
Author(s):  
N. Economopoulos ◽  
N. Athanassopoulos ◽  
N. A. Katsanos ◽  
G. Karaiskakis ◽  
P. Agathonos ◽  
...  

1995 ◽  
Vol 41 (3-4) ◽  
pp. 227-235
Author(s):  
I. Topalova ◽  
A. Niotis ◽  
N. A. Katsanos ◽  
V. Sotiropoulou

Food Control ◽  
2016 ◽  
Vol 67 ◽  
pp. 255-264 ◽  
Author(s):  
Qin Guo ◽  
Fan He ◽  
Qingpeng Li ◽  
Zhaoxuan Deng ◽  
Jing Jin ◽  
...  

2010 ◽  
Vol 178 ◽  
pp. 65-70 ◽  
Author(s):  
Sheng Rui Xu ◽  
Qin Shuai ◽  
Jin Hua Cheng ◽  
Xiao Ge Wang

A new catalyst of gold supported on nanometal oxide for oxidation of SO2 was developed. Deposition-precipitation method was used to prepare gold-based catalysts. The catalytic activity of the catalysts was evaluated by determining the concentration of SO2 with gas chromatography under reaction temperature from 100 to 700°C. The results showed that there was an enhancement of catalytic activity when gold nanoparticles were dispersed on the surface of nano-metal oxides, furthermore, γ-Fe2O3 showed the highest activity as the support of the colloidal gold supported catalysts among the nanometal oxides including γ-Fe2O3, Fe2O3, ZnO, and Al2O3. It was also found that water vapour in the reaction enhanced the catalytic activity of Au/γ-Fe2O3. The Au/γ-Fe2O3 was characterized by XRD and FTIR methods, which indicated that the gold nanoparticles were dispersed on the γ-Fe2O3 support and sulfate species were formed on the surface of catalysts.


2014 ◽  
Vol 26 (23) ◽  
pp. 7871-7876 ◽  
Author(s):  
H.H. Mohammad ◽  
Khalisanni Khalid ◽  
Sharifuddin Mohd. Zain

Materials ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 812
Author(s):  
Louay Al-Hussaini ◽  
Franck Launay ◽  
Elena Galvez

This work deals with the aerobic oxidative cleavage of C-C and C-O bonds catalyzed by the Keggin-type phosphovanadomolybdic acid (H6[PMo9V3O40], noted H6PV3). The latter was synthesized by an adapted hydrothermal procedure classically used for lower vanadium content and was tested as a catalyst for the aerobic cleavage of 2-phenoxyacetophenone (noted K1HH) and 1-phenyl-2-phenoxyethanol (A1HH) used as two lignin models. The operative conditions (solvent, catalytic loading, etc.) were adjusted on K1HH and extrapolated to A1HH. The cleavage of the alcohol model required more drastic conditions and therefore further optimization. Preliminary attempts on an Organosolv wheat straw lignin were performed too. From the kinetic study, high performance liquid chromatography (HPLC) and gas chromatography–mass spectrometry (GC-MS) data, a mechanism of the cleavage of both models was proposed.


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