Oxidative and non-oxidative degradation of C1-C3 carboxylic acids over V2O5/TiO2 and MoVTeNb oxides: A comparative study

被引:7
作者
Sobolev, Vladimir I. [1 ]
Koltunov, Konstantin Yu. [1 ,2 ]
机构
[1] Russian Acad Sci, Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[2] Novosibirsk State Univ, Novosibirsk 630090, Russia
关键词
V2O5/TiO2; Mo-V-Te-Nb mixed oxides; Formic acid; Acetic acid; Propionic acid; Degradation; Oxidative degradation; ACETIC-ACID; FORMIC-ACID; SELECTIVE OXIDATION; MIXED OXIDES; CATALYSTS; MO; DECOMPOSITION; ETHANOL; WATER; DECARBONYLATION;
D O I
10.1016/j.apcata.2013.06.018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Carboxylic acids are valuable chemical products, which can be produced efficiently by catalytic oxidation of various organic compounds using vanadium-based catalysts. Degradation resistance of carboxylic acids under applied reaction conditions is an important factor influencing selectivity of such reactions. This paper addresses the oxidative and non-oxidative gas phase degradation of formic, acetic and propionic acids over V2O5/TiO2 and MoVTeNb mixed oxides. Formic acid has been found to undergo mainly acid catalyzed decarbonylation, regardless the presence or absence of oxygen in the feed. Both acetic and propionic acids underwent oxidation (in aerobic conditions) through one-carbon degradation steps until CO and CO2 were produced. The mechanistic aspects of these transformations are discussed. The key intermediacy of 2-(hydro)peroxy carboxylic acids is suggested, based on the nature of primary reaction products. The catalytic activity of MoVTeNb mixed oxides toward oxidative and non-oxidative degradation of acetic and propionic acids appeared notably lower compared to that of V2O5/TiO2. This may be linked to the enhanced efficiency of the former catalyst in selective oxidation of organic substrates to carboxylic acids. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 50
页数:6
相关论文
共 41 条
[1]   An efficient conversion of carboxylic acids to one-carbon degraded aldehydes via 2-hydroperoxy acids [J].
Akakabe, Yoshihiko ;
Nyuugaku, Takeshi .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2007, 71 (05) :1370-1371
[2]   Organic reactions at well-defined oxide surfaces [J].
Barteau, MA .
CHEMICAL REVIEWS, 1996, 96 (04) :1413-1430
[3]   Organic Peracids: A Structural Puzzle for 17O NMR and Ab Initio Chemical Shift Calculations [J].
Castiglione, Franca ;
Baggioli, Alberto ;
Citterio, Attilio ;
Mele, Andrea ;
Raos, Guido .
JOURNAL OF PHYSICAL CHEMISTRY A, 2012, 116 (07) :1814-1819
[4]   Oxidation of Carboxylic Acids Regenerates Hydroxyl Radicals in the Unpolluted and Nighttime Troposphere [J].
da Silva, Gabriel .
JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (25) :6861-6869
[5]   Thermal Hydrogen-Atom Transfer from Methane: The Role of Radicals and Spin States in Oxo-Cluster Chemistry [J].
Dietl, Nicolas ;
Schlangen, Maria ;
Schwarz, Helmut .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (23) :5544-5555
[6]   SELECTIVE REDUCTION OF ACETIC-ACID TO ACETALDEHYDE ON IRON-OXIDES [J].
GROOTENDORST, EJ ;
PESTMAN, R ;
KOSTER, RM ;
PONEC, V .
JOURNAL OF CATALYSIS, 1994, 148 (01) :261-269
[7]  
Gubelmann-Bonneau M., 1998, U.S. Patent, Patent No. [5,840,971, 5840971]
[8]   Gas-phase decomposition of formic acid over α-Fe2O3 catalysts [J].
Halawy, SA ;
Al-Shihry, SS ;
Mohamed, MA .
CATALYSIS LETTERS, 1997, 48 (3-4) :247-251
[9]   Oxide-catalyzed conversion of acetic acid into acetone: an FTIR spectroscopic investigation [J].
Hasan, MA ;
Zaki, MI ;
Pasupulety, L .
APPLIED CATALYSIS A-GENERAL, 2003, 243 (01) :81-92
[10]   OXIDATION BY METAL SALTS .2. FORMATION OF GAMMA-LACTONES BY REACTION OF LEAD TETRAACETATE WITH OLEFINS IN ACETIC ACID [J].
HEIBA, EI ;
DESSAU, RM ;
KOEHL, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (10) :2706-&