Standard

Formic acid decomposition over V-Ti oxide catalyst : Mechanism and kinetics. / Sadovskaya, E. M.; Chesalov, Yu A.; Goncharov, V. B. и др.

в: Molecular Catalysis, Том 430, 04.2017, стр. 54-62.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Sadovskaya, EM, Chesalov, YA, Goncharov, VB, Sobolev, VI & Andrushkevich, TV 2017, 'Formic acid decomposition over V-Ti oxide catalyst: Mechanism and kinetics', Molecular Catalysis, Том. 430, стр. 54-62. https://doi.org/10.1016/j.molcata.2016.12.010

APA

Sadovskaya, E. M., Chesalov, Y. A., Goncharov, V. B., Sobolev, V. I., & Andrushkevich, T. V. (2017). Formic acid decomposition over V-Ti oxide catalyst: Mechanism and kinetics. Molecular Catalysis, 430, 54-62. https://doi.org/10.1016/j.molcata.2016.12.010

Vancouver

Sadovskaya EM, Chesalov YA, Goncharov VB, Sobolev VI, Andrushkevich TV. Formic acid decomposition over V-Ti oxide catalyst: Mechanism and kinetics. Molecular Catalysis. 2017 апр.;430:54-62. doi: 10.1016/j.molcata.2016.12.010

Author

Sadovskaya, E. M. ; Chesalov, Yu A. ; Goncharov, V. B. и др. / Formic acid decomposition over V-Ti oxide catalyst : Mechanism and kinetics. в: Molecular Catalysis. 2017 ; Том 430. стр. 54-62.

BibTeX

@article{b0211ca847754380b0dfe3bff3197e14,
title = "Formic acid decomposition over V-Ti oxide catalyst: Mechanism and kinetics",
abstract = "A detailed kinetic model for formic acid (HCOOH) decomposition on oxide vanadium-titanium (7.3%V2O5/92.7%TiO2) catalyst has been developed based on transient kinetic studies and IR spectroscopy in situ. Formic acid decomposition to CO2 (dehydrogenation) and to CO (dehydration) proceeds via different mechanistic routes. Dehydrogenation proceeds via the conventional “formate” mechanism and include reversible dissociative adsorption of formic acid on vanadyl group V = O. The oxygen of the group acts as a proton acceptor whereas a vanadium cation is a formate anion stabilizer. Formate complexes can recombinate with protons and desorb in the form of formic acid or decompose to CO2. Dehydration reaction follows a different mechanism. An interaction of the coordination unsaturated sites V+-O− with HCOOH leads to the synchronous cleavage of the C–OH and C–H bonds. Meanwhile the two OH hydroxyl groups are formed and CO molecule is evolved into gas phase. The path is completed by water desorption. The rate constants and activation energies of elementary steps are calculated for a dehydrogenation and dehydration reactions. The rate-limited steps of the reaction are formate decomposition stage for dehydrogenation path (Ea = 60 kJ/mol) and water desorption stage for dehydration rout (Ea = 100 kJ/mol). The difference in the values of activation energies results in an increase of selectivity towards CO with reaction temperature elevation. Water inhibits formic acid decomposition. In the case the dehydrogenation, it connected with adsorption displacement of formates with water, whereas, in the case of dehydration, it is associated with an active centers blocking by adsorbed water. The developed kinetic model takes into account the water effect of both routs and satisfactorily describes the steady state reaction behavior.",
keywords = "Formic acid decomposition, IR spectroscopy, Transient kinetic, V-Ti oxide catalyst, OXIDATION, IR, RAMAN, V2O5/TIO2 CATALYSTS, ADSORPTION, DFT, FORMALDEHYDE, WATER, SURFACES",
author = "Sadovskaya, {E. M.} and Chesalov, {Yu A.} and Goncharov, {V. B.} and Sobolev, {V. I.} and Andrushkevich, {T. V.}",
year = "2017",
month = apr,
doi = "10.1016/j.molcata.2016.12.010",
language = "English",
volume = "430",
pages = "54--62",
journal = "Molecular Catalysis",
issn = "2468-8231",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Formic acid decomposition over V-Ti oxide catalyst

T2 - Mechanism and kinetics

AU - Sadovskaya, E. M.

AU - Chesalov, Yu A.

AU - Goncharov, V. B.

AU - Sobolev, V. I.

AU - Andrushkevich, T. V.

PY - 2017/4

Y1 - 2017/4

N2 - A detailed kinetic model for formic acid (HCOOH) decomposition on oxide vanadium-titanium (7.3%V2O5/92.7%TiO2) catalyst has been developed based on transient kinetic studies and IR spectroscopy in situ. Formic acid decomposition to CO2 (dehydrogenation) and to CO (dehydration) proceeds via different mechanistic routes. Dehydrogenation proceeds via the conventional “formate” mechanism and include reversible dissociative adsorption of formic acid on vanadyl group V = O. The oxygen of the group acts as a proton acceptor whereas a vanadium cation is a formate anion stabilizer. Formate complexes can recombinate with protons and desorb in the form of formic acid or decompose to CO2. Dehydration reaction follows a different mechanism. An interaction of the coordination unsaturated sites V+-O− with HCOOH leads to the synchronous cleavage of the C–OH and C–H bonds. Meanwhile the two OH hydroxyl groups are formed and CO molecule is evolved into gas phase. The path is completed by water desorption. The rate constants and activation energies of elementary steps are calculated for a dehydrogenation and dehydration reactions. The rate-limited steps of the reaction are formate decomposition stage for dehydrogenation path (Ea = 60 kJ/mol) and water desorption stage for dehydration rout (Ea = 100 kJ/mol). The difference in the values of activation energies results in an increase of selectivity towards CO with reaction temperature elevation. Water inhibits formic acid decomposition. In the case the dehydrogenation, it connected with adsorption displacement of formates with water, whereas, in the case of dehydration, it is associated with an active centers blocking by adsorbed water. The developed kinetic model takes into account the water effect of both routs and satisfactorily describes the steady state reaction behavior.

AB - A detailed kinetic model for formic acid (HCOOH) decomposition on oxide vanadium-titanium (7.3%V2O5/92.7%TiO2) catalyst has been developed based on transient kinetic studies and IR spectroscopy in situ. Formic acid decomposition to CO2 (dehydrogenation) and to CO (dehydration) proceeds via different mechanistic routes. Dehydrogenation proceeds via the conventional “formate” mechanism and include reversible dissociative adsorption of formic acid on vanadyl group V = O. The oxygen of the group acts as a proton acceptor whereas a vanadium cation is a formate anion stabilizer. Formate complexes can recombinate with protons and desorb in the form of formic acid or decompose to CO2. Dehydration reaction follows a different mechanism. An interaction of the coordination unsaturated sites V+-O− with HCOOH leads to the synchronous cleavage of the C–OH and C–H bonds. Meanwhile the two OH hydroxyl groups are formed and CO molecule is evolved into gas phase. The path is completed by water desorption. The rate constants and activation energies of elementary steps are calculated for a dehydrogenation and dehydration reactions. The rate-limited steps of the reaction are formate decomposition stage for dehydrogenation path (Ea = 60 kJ/mol) and water desorption stage for dehydration rout (Ea = 100 kJ/mol). The difference in the values of activation energies results in an increase of selectivity towards CO with reaction temperature elevation. Water inhibits formic acid decomposition. In the case the dehydrogenation, it connected with adsorption displacement of formates with water, whereas, in the case of dehydration, it is associated with an active centers blocking by adsorbed water. The developed kinetic model takes into account the water effect of both routs and satisfactorily describes the steady state reaction behavior.

KW - Formic acid decomposition

KW - IR spectroscopy

KW - Transient kinetic

KW - V-Ti oxide catalyst

KW - OXIDATION

KW - IR

KW - RAMAN

KW - V2O5/TIO2 CATALYSTS

KW - ADSORPTION

KW - DFT

KW - FORMALDEHYDE

KW - WATER

KW - SURFACES

UR - http://www.scopus.com/inward/record.url?scp=85029627007&partnerID=8YFLogxK

U2 - 10.1016/j.molcata.2016.12.010

DO - 10.1016/j.molcata.2016.12.010

M3 - Article

AN - SCOPUS:85029627007

VL - 430

SP - 54

EP - 62

JO - Molecular Catalysis

JF - Molecular Catalysis

SN - 2468-8231

ER -

ID: 10068777