Sciact
  • EN
  • RU

FTIR Study of β-Picoline and Pyridine-3-Carbaldehyde Transformation on V–Ti–O Catalysts. The Effect of Sulfate Content on β-Picoline Oxidation into Nicotinic Acid Full article

Journal Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Output data Year: 2013, Volume: 380, Pages: 118-130 Pages count : 13 DOI: 10.1016/j.molcata.2013.09.028
Tags FTIR spectroscopy, Nicotinic acid, Sulfates, Vanadia-titania catalysts, β-Picoline oxidation
Authors Chesalov Yuriy A. 1 , Andrushkevich Tamara V. 1 , Sobolev Vladimir I. 1 , Chernobay Galina B. 1
Affiliations
1 Boreskov Institute of Catalysis, Russian Academy of Sciences, Prosp. Lavrentieva, 5, Novosibirsk 630090, Russian Federation

Abstract: Surface complexes of β-picoline, 3-pyridine-carbaldehyde and nicotinic acid on 20 wt.% V2O5/TiO2 catalysts containing 0.07 and 6.3l wt.% SO42− were studied by FTIR spectroscopy and temperature programmed reaction technique. The water (both H2O and D2O), pyridine and β-picoline were used as molecular probes for identification of surface acidity and the structure of sulfate species. Both samples possess Lewis and Brönsted acidic sites. β-Picoline, 3-pyridine-carbaldehyde and nicotinic acid form surface complexes of similar structure on both studied catalysts. But high sulfated catalyst contains stronger Brönsted sites in greater amount. It leads to the formation of stronger bound surface complexes of β-picoline, 3-pyridine-carbaldehyde and nicotinic acid. The strongly bound surface complexes are transformed into by-products (COx, pyridine and 3-cyanopyridine). It resulted in substantial reduction of nicotinic acid yield.
Cite: Chesalov Y.A. , Andrushkevich T.V. , Sobolev V.I. , Chernobay G.B.
FTIR Study of β-Picoline and Pyridine-3-Carbaldehyde Transformation on V–Ti–O Catalysts. The Effect of Sulfate Content on β-Picoline Oxidation into Nicotinic Acid
Journal of Molecular Catalysis A: Chemical. 2013. V.380. P.118-130. DOI: 10.1016/j.molcata.2013.09.028 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jul 1, 2013
Accepted: Sep 20, 2013
Published online: Oct 1, 2013
Published print: Dec 1, 2013
Identifiers:
Web of science: WOS:000327686600017
Scopus: 2-s2.0-84886002558
Elibrary: 21883338
Chemical Abstracts: 2013:1748619
Chemical Abstracts (print): 160:33526
OpenAlex: W2024808497
Citing:
DB Citing
Web of science 13
Scopus 14
Elibrary 12
OpenAlex 11
Altmetrics: