scholarly journals Vapor Phase Ammoxidation of 4-Phenyl-o-Xylene into 4-Phenylphthalonitrile on V–Sb–Bi–Zr/<i>γ</i>-Al<sub>2</sub>O<sub>3</sub> Oxide Catalyst

2015 ◽  
Vol 04 (03) ◽  
pp. 59-67 ◽  
Author(s):  
Gulu A. Bagirzade ◽  
Dilgam B. Taghiyev ◽  
Manaf R. Manafov
Keyword(s):  
1969 ◽  
Vol 47 (3) ◽  
pp. 284-287 ◽  
Author(s):  
I. S. Jaswal ◽  
R. F. Mann ◽  
J. A. Juusola ◽  
J. Downie

2017 ◽  
Vol 6 (2) ◽  
pp. 127
Author(s):  
D.Kh. Sembaev ◽  
O.K. Yugay ◽  
S.G. Klepikova

<p>The vapor phase oxidation of 2-methyl-5-ethylpyridine (MEP) on modified vanadium oxide catalyst has been investigated. Di(5-ethyl)-2-pyridil, 2-methyl-5-acethylpyridine and 3-acethylpyridine have been identified as intermediates of MEP oxidation by NMR <sup>13</sup>C spectroscopic and gas chromatography mass spectrometry methods. It has been shown that the interaction between the pyridine base and acidic proton donating sites on the catalyst surface causes an increase of substituents reactivity in 2-position in all stages of 2-methyl-5-ethylpyridine transformation inducing their oxidative elimination. A distinction in composition of the oxidation products is an outcome of a change of the dialkylpyridine substituents in 2- and 5-position contribution. Using literature and experimental data the basic routes of the 2-methyl-5-ethylpyridine oxidative conversion have been determined. The ammoxidation is a process based on the joint oxidation of the initial organic substance and ammonia by air oxygen in the presence of a catalyst [1]. The basic step of ammoxidation is a vapor phase catalytic oxidation, which determines the main routes of the former. Therefore, the obtained results give a possibility for the first time to explain the reason for the change of selectivities during MEP ammoxidation in the present of water.</p>


1977 ◽  
Vol 6 (4) ◽  
pp. 461-466 ◽  
Author(s):  
W. Krajewski ◽  
J. Skryzpek ◽  
A. Gawdzik ◽  
J. Aerts ◽  
H. Herman ◽  
...  

1980 ◽  
Vol 15 (2) ◽  
pp. 251-255 ◽  
Author(s):  
R. A. Skolmeistere ◽  
O. V. Orbidane ◽  
L. J. Leitis ◽  
M. V. Shimanskaya

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yanting Liu ◽  
Ran Wang ◽  
Haifeng Qi ◽  
Xiao Yan Liu ◽  
Guangyi Li ◽  
...  

AbstractThe exploration of highly efficient processes to convert renewable biomass to fuels and value-added chemicals is stimulated by the energy and environment problems. Herein, we describe an innovative route for the production of methylcyclopentadiene (MCPD) with cellulose, involving the transformation of cellulose into 3-methylcyclopent-2-enone (MCP) and subsequent selective hydrodeoxygenation to MCPD over a zinc-molybdenum oxide catalyst. The excellent performance of the zinc-molybdenum oxide catalyst is attributed to the formation of ZnMoO3 species during the reduction of ZnMoO4. Experiments reveal that preferential interaction of ZnMoO3 sites with the C=O bond instead of C=C bond in vapor-phase hydrodeoxygenation of MCP leads to highly selective formations of MCPD (with a carbon yield of 70%).


2018 ◽  
Vol 58 (1) ◽  
pp. 101-109 ◽  
Author(s):  
Xinli Li ◽  
Jun Pang ◽  
Ju Zhang ◽  
Chunyu Yin ◽  
Weixin Zou ◽  
...  

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