Acetalization of glycerol using mesoporous MoO3/SiO2 solid acid catalyst

Abstract Acetalization of glycerol with various aldehydes has been carried out using mesoporous MoO3/SiO2 as a solid acid catalyst. A series of MoO3/SiO2 catalysts with varying MoO3 loadings (1–20 mol%) were prepared by sol–gel technique using ethyl silicate-40 and ammonium heptamolybdate as silica and molybdenum source respectively. The sol–gel derived samples were calcined at 500 °C and characterized using various physicochemical characterization techniques. The XRD of the calcined samples showed the formation of amorphous phase up to 10 mol% MoO3 loading and at higher loading of crystalline α-MoO3 on amorphous silica support. TEM analyses of the materials showed the uniform distribution of MoO3 nanoparticles on amorphous silica support. Raman spectroscopy showed the formation of silicomolybdic acid at low Mo loading and a mixture of α-MoO3 and polymolybdate species at high Mo loadings. Moreover the Raman spectra of intermediate loading samples also suggest the presence of β-MoO3. Acetalization of glycerol with benzaldehyde was carried out using series of MoO3/SiO2 catalysts with varying MoO3 loadings (1–20 mol%). Among the series, MoO3/SiO2 with 20 mol% MoO3 loadings was found to be the most active catalyst in acetalization under mild conditions. Maximum conversion of benzaldehyde (72%) was obtained in 8 h at 100 °C with 60% selectivity for the six-membered acetal using 20% MoO3/SiO2. Interestingly with substituted benzaldehydes under same reaction conditions the conversion of aldehydes decreased with increase in selectivity for six-membered acetals. These results indicate the potential of this catalyst for the acetalization of glycerol for an environmentally benign process.

[1]  A. Corma,et al.  Zeolites for the Production of Fine Chemicals: Synthesis of the Fructone Fragrancy , 2000 .

[2]  Toru Iida,et al.  Acrolein synthesis from glycerol in hot-compressed water. , 2007, Bioresource technology.

[3]  B. Rebours,et al.  Raman spectroscopic evidence for the formation of silicomolybdic entities on a Mo/HY zeolite catalyst , 2005 .

[4]  A. Corma,et al.  Synthesis of hyacinth, vanilla, and blossom orange fragrances: the benefit of using zeolites and delaminated zeolites as catalysts , 2004 .

[5]  N. Azuma,et al.  Effects of Catalyst Heating Rates Upon the Activity of Silica-Supported Silicomolybdic Acid Catalysts for Methane Partial Oxidation , 2002 .

[6]  R. Gonzalez,et al.  Anaerobic fermentation of glycerol: a path to economic viability for the biofuels industry. , 2007, Current opinion in biotechnology.

[7]  J. Grimblot,et al.  Genesis and activity of mo-based hydrotreating catalysts prepared by a sol-gel method , 1994 .

[8]  J. Lassègues,et al.  Infrared and Raman spectra of MoO 3 molybdenum trioxides and MoO 3 · xH 2O molybdenum trioxide hydrates , 1995 .

[9]  A. Bell,et al.  Selective oxidation of methane over MoOx/SiO2: isolation of the kinetics of reactions occurring in the gas phase and on the surfaces of SiO2 and MoOx , 2005 .

[10]  A. Corma,et al.  Design of a solid catalyst for the synthesis of a molecule with blossom orange scent , 2002 .

[11]  A. Showler,et al.  Condensation products of glycerol with aldehydes and ketones. 2-Substituted m-dioxan-5-ols and 1,3-dioxolane-4-methanols. , 1967, Chemical reviews.

[12]  Arno Behr,et al.  Improved utilisation of renewable resources: New important derivatives of glycerol , 2008 .

[13]  M. Dongare,et al.  Transesterification of diethyl oxalate with phenol using MoO3/SiO2 catalyst , 2005 .

[14]  H. Vogel,et al.  Catalytic dehydration of glycerol in sub- and supercritical water: a new chemical process for acrolein production , 2006 .

[15]  J. Stencel Raman spectroscopy for catalysis , 1990 .

[16]  A. Corma,et al.  Formation and hydrolysis of acetals catalysed by acid Faujasites , 1990 .

[17]  R. Keiski,et al.  Direct synthesis of dimethyl carbonate with supercritical carbon dioxide: Characterization of a key organotin oxide intermediate , 2006 .

[18]  A. Marshall,et al.  Production of hydrogen by the electrochemical reforming of glycerol–water solutions in a PEM electrolysis cell , 2008 .

[19]  Rafael van Grieken,et al.  Acidic Mesoporous Silica for the Acetylation of Glycerol: Synthesis of Bioadditives to Petrol Fuel , 2007 .

[20]  A. Corma,et al.  Al-free Sn-Beta zeolite as a catalyst for the selective reduction of carbonyl compounds (Meerwein-Ponndorf-Verley reaction). , 2002, Journal of the American Chemical Society.

[21]  Á. Németh,et al.  Development of a New Bioprocess for Production of 1,3-propanediol I.: Modeling of Glycerol Bioconversion to 1,3-propanediol with Klebsiella pneumoniae Enzymes , 2008, Applied biochemistry and biotechnology.

[22]  P. Hodge,et al.  Protective groups in organic synthesis , 1981 .

[23]  M. Pagliaro,et al.  From glycerol to value-added products. , 2007, Angewandte Chemie.

[24]  P. Patil,et al.  Solid acid catalysts for fluorotoluene nitration using nitric acid , 2003 .

[25]  Anti-inflammatory 17β-Thioalkyl-16α,17α-ketal and -acetal Androstanes: A New Class of Airway Selective Steroids for the Treatment of Asthma , 1996 .

[26]  Shengping Wang,et al.  Reactivity and surface properties of silica supported molybdenum oxide catalysts for the transesterification of dimethyl oxalate with phenol , 2004 .

[27]  J. Barbe,et al.  Heterocyclic acetals from glycerol and acetaldehyde in Port wines: evolution with aging. , 2002, Journal of agricultural and food chemistry.

[28]  A. Corma,et al.  Use of delaminated zeolites (ITQ-2) and mesoporous molecular sieves in the production of fine chemicals: Preparation of dimethylacetals and tetrahydropyranylation of alcohols and phenols , 2000 .

[29]  Naoki Sawamura,et al.  Highly effective acetalization of aldehydes and ketones with methanol on siliceous mesoporous material , 1998 .

[30]  P. Patil,et al.  Vapor phase nitration of benzene using mesoporous MoO3/SiO2 solid acid catalyst , 2006 .

[31]  J. Ekerdt,et al.  Relationship between structure and point of zero surface charge for molybdenum and tungsten oxides supported on alumina , 1992 .

[32]  R. Maggi,et al.  1,3-Dioxolanes from carbonyl compounds over zeolite HSZ-360 as a reusable heterogeneous catalyst , 1998 .

[33]  H. Lieske,et al.  Investigations on heterogeneously catalysed condensations of glycerol to cyclic acetals , 2007 .

[34]  T. Hartman,et al.  Mass Spectrometry of the Acetal Derivatives of Selected Generally Recognized as Safe Listed Aldehydes with Ethanol, 1,2-Propylene Glycol and Glycerol , 1998 .

[35]  P. Patil,et al.  Regioselective nitration of o-xylene to 4-nitro-o-xylene using nitric acid over solid acid catalysts , 2003 .

[36]  E. Mccarron β-MoO3: a metastable analogue of WO3 , 1986 .

[37]  M. Dongare,et al.  Regioselective nitration of cumene to 4-nitro cumene using nitric acid over solid acid catalyst , 2006 .

[38]  A. Corma,et al.  Sn-zeolite beta as a heterogeneous chemoselective catalyst for Baeyer–Villiger oxidations , 2001, Nature.

[39]  S. Launay,et al.  Catalysis by 12-molybdophosphates. 1. Catalytic reactivity of 12-molybdophosphoric acid related to its thermal behavior investigated through IR, Raman, polarographic, and X-ray diffraction studies : A comparison with 12-molybdosilicic acid , 1996 .

[40]  C. Ramana,et al.  Silica supported MoO3: a mild heterogeneous catalyst for the Beckmann rearrangement and its application to some sugar derived ketoximes , 2004 .

[41]  A. Corma,et al.  Use of Mesoporous MCM-41 Aluminosilicates as Catalysts in the Production of Fine Chemicals: Preparation of Dimethylacetals , 1996 .

[42]  A. Loupy,et al.  Liquid crystalline 5,6-O-acetals of L-galactono-1,4-lactone prepared by a microwave irradiation on montmorillonite , 1993 .