MoO3/SO42−-TiO2 catalyst for transesterification of dimethyl cabonate with phenol

Li-ping Cui , Yan-jun Li , Zhong Li , Jun-fu Zhao

Journal of Central South University ›› 2014, Vol. 21 ›› Issue (5) : 1719 -1724.

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Journal of Central South University ›› 2014, Vol. 21 ›› Issue (5) : 1719 -1724. DOI: 10.1007/s11771-014-2115-0
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MoO3/SO42−-TiO2 catalyst for transesterification of dimethyl cabonate with phenol

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Abstract

A new MoO3/SO42−-TiO2 catalyst was prepared by a conventional impregnation of SO42−/TiO2 as carrier with an aqueous solution of ammonium molybdate and used for the synthesis of transesterification of dimethyl carbonate (DMC) with phenol. A series of MoO3/SO42−-TiO2 catalysts with different MoO3 loadings were investigated and characterized using X-ray diffraction (XRD), Fourier transform infrared spectrometer (FTIR), NH3-temperature programmed desorption (NH3-TPD) and X-ray photoelectron spectroscopy (XPS). The results show that MoO3 loading is related to the activity of transesterification reaction. With the increase of MoO3 loading, the activity of transesterification reaction increases. The sulfur species in the catalyst have an influence on the molybdenum species, and lead to an increase in the electropositive of molybdenum, which promotes the catalytic activity of MoO3/SO42−-TiO2. Among the series of catalysts prepared, MoO3/SO42−-TiO2 with 10% MoO3 and 823 K calcinated is found to be the most active catalyst for transesterification reaction. Under the reaction conditions of 453 K and 12 h, the conversion of DMC is 30.5 %, and the yields of MPC and DPC reach 21.2 % and 8.7 %, respectively.

Keywords

dimethyl carbonate / diphenyl carbonate / transesterification / MoO3

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Li-ping Cui, Yan-jun Li, Zhong Li, Jun-fu Zhao. MoO3/SO42−-TiO2 catalyst for transesterification of dimethyl cabonate with phenol. Journal of Central South University, 2014, 21(5): 1719-1724 DOI:10.1007/s11771-014-2115-0

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References

[1]

DelledonneD, RivettiF, RomanoU. Developments in the production and application of dimethylcarbonate [J]. Applied Catalysis A: General, 2001, 221(1/2): 241-251

[2]

ElectieGProcess for making dioryl carbonates: EP, 1987

[3]

ChenT, HanH-j, YaoJ, WangG-ying. The transesterification of dimethyl carbonate and phenol catalyzed by 12-molybdophosphoric salts [J]. Catalysis Communications, 2007, 8(9): 1361-1365

[4]

YangX-j, HanJ-y, DuZ-p, YuanH, JinF, WuY-xin. Effects of Pb dopant on structure and activity of Pd/K-OMS-2 catalysts for heterogeneous oxidative carbonylation of phenol [J]. Catalysis Communications, 2010, 11(7): 643-646

[5]

YongT K, EunD P. Transesterification between dimethyl carbonate and phenol in the presence of (NH4)8Mo10O34 as a catalyst precursor [J]. Applied Catalysis A: General, 2009, 361(1/2): 26-31

[6]

CaoM, MengY-z, LuY-xin. Synthesis of diphenyl carbonate from dimethyl carbonate and phenol using O2-promoted PbO/MgO catalysts [J]. Catalysis Communications, 2005, 6(12): 802-807

[7]

LeeH, Joon KimS, Sung AhnB, Koo LeeW, Sik KimH. Role of sulfonic acids in the Sn-catalyzed transesterification of dimethyl carbonate with phenol [J]. Catalysis Today, 2003, 87(1/2/3/4): 139-144

[8]

DuZ-p, XiaoY-h, ChenT, WangG-ying. Catalytic study on the transesterification of dimethyl carbonate and phenol to diphenyl carbonate [J]. Catalysis Communications, 2008, 9(2): 239-243

[9]

GaoJ-j, YaoJ, MeiH, WangG-ying. Transesterification of dimethyl carbonate and phenol with titanate catalysts [J]. Chinese Journal of Catalysis, 2001, 22(4): 405-407

[10]

KimW B, KimY G, LeeJ S. The role of carbon deposition in the gas phase transesterification of dimethylcarbonate and phenol over TiO2/SiO2 catalyst [J]. Applied Catalysis A: General, 2000, 194–195(0): 403-414

[11]

ZhouW-q, ZhaoX-q, WangY-j, ZhangJ-yan. Synthesis of diphenyl carbonate by transesterification over lead and zinc double oxide catalyst [J]. Applied Catalysis A: General, 2004, 260(1): 19-24

[12]

WangS, BaiR-x, MeiF-m, LiG-xing. Pyroaurite as an active, reusable and environmentally benign catalyst in synthesis of diphenyl carbonate by transesterification [J]. Catalysis Communications, 2009, 11(3): 202-205

[13]

CaoP, YangX-g, TangC-m, YangJ, YaoJ, WangY, WangG-ying. Molybdenum trioxide catalyst for transesterification of dimethyl carbonate and phenyl acetate to diphenyl carbonate [J]. Chinese Journal of Catalysis, 2009, 30(9): 853-855

[14]

BiradarA V, UmbarkarS B, DongareM K. Transesterification of diethyl oxalate with phenol using MoO3/SiO2 catalyst [J]. Applied Catalysis A: General, 2005, 285(1/2): 190-195

[15]

ZhangL-p, ZhuH-y, LiX-w, WanH-q, DongLin. Dispersion behaviors of molybdena on SO42−-modified TiO2 (Rutile and/or Anatase) [J]. Chinese Journal of Inorganic Chemistry, 2007, 23(4): 577-583

[16]

PizzioL R. Mesoporous titania: Effect of thermal treatment on the texture and acidic properties [J]. Materials Letters, 2005, 59(8/9): 994-997

[17]

El ShafeiG M S, MokhtarM. Interaction between molybdena and silica: FT-IR/PA studies of surface hydroxyl groups and pore structure assessment [J]. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 1995, 94(2/3): 267-277

[18]

SeguinL, FiglarzM, CavagnatR, LassèguesJ C. Infrared and Raman spectra of MoO3 molybdenum trioxides and MoO3xH2O molybdenum trioxide hydrates [J]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1995, 51(8): 1323-1344

[19]

ArenaF, GiordanoN, ParmalianaA. Working mechanism of oxide catalysts in the partial oxidation of methane to formaldehyde. II. Redox properties and reactivity of SiO2, MoO3/SiO2, V2O5/SiO2, TiO2, and V2O5/TiO2 systems [J]. Journal of Catalysis, 1997, 167(1): 66-76

[20]

SuW-y, FuX-z, WeiK-mei. Raman and infrared spectroscopic investigation of SO42−/TiO2 solid acids [J]. Spectroscopy and Spectral Analysis, 2000, 20(6): 840-841

[21]

YangS-j, LiangY-g, YuX-q, SunJ-tang. Preparation of SO42−/TiO2-MoO3 solid superacid and its catalytic activity in acetalation and ketalation [J]. Chinese Journal of Chemical Engineering, 2005, 13(1): 57-61

[22]

SuW-y, ChenY-l, FuX-z, WeiK-mei. Acid strength and photocatalytic activity of SO42−/TiO2 solid acid catalyst [J]. Chinese Journal of Catalysis, 2001, 22(2): 175-176

[23]

BarthosR, LónyiF, OnyestyákG, ValyonJ. An IR, FR, and TPD study on the acidity of H-ZSM-5, sulfated zirconia, and sulfated zirconia-titania using ammonia as the probe molecule [J]. The Journal of Physical Chemistry B, 2000, 104(31): 7311-7319

[24]

LiZ, HuangH-b, XieK-chang. Preparation and characterization of Cu(I)/SO42−/ZnO and Cu(I)/S2O82−/ZnO catalysts [J]. Chemical Journal of Chinese Universities-Chinese, 2008, 29(8): 1609-1615

[25]

ChoiJ G, ThompsonL T. XPS study of as-prepared and reduced molybdenum oxides [J]. Applied Surface Science, 1996, 93(2): 143-149

[26]

CiambelliP, SanninoD, PalmaV, VaianoV, EloyP, DuryF, GaigneauxE M. Tuning the selectivity of MoOx supported catalysts for cyclohexane photo oxidehydrogenation [J]. Catalysis Today, 2007, 128(3/4): 251-257

[27]

FuZ-h, OnoY. Two-step synthesis of diphenyl carbonate from dimethyl carbonate and phenol using MoO3SiO2 catalysts [J]. Journal of Molecular Catalysis A: Chemical, 1997, 118(3): 293-299

[28]

LiZ-h, ChengB-w, SuK-m, GuY, XiP, GuoM-lin. The synthesis of diphenyl carbonate from dimethyl carbonate and phenol over mesoporous MoO3/SiMCM-41 [J]. Journal of Molecular Catalysis A: Chemical, 2008, 289(1/2): 100-105

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