Solvothermal synthesis of vanadium phosphate catalysts for n-butane oxidation

被引:26
作者
Rownaghi, Asghar [1 ]
Taufiq-Yap, Yun Hin [2 ]
Rezaei, Fateme [1 ]
机构
[1] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
[2] Univ Putra Malaysia, Dept Chem, Selangor 43400, Malaysia
关键词
Vanadium phosphate; Vanadyl hydrogen phosphate hemihydrate; Solvothermal synthesis; High pressure autoclave; Microwave heating; Primary alcohol; n-Butane oxidation; P-O CATALYSTS; PHOSPHORUS OXIDE CATALYSTS; MALEIC-ANHYDRIDE; SELECTIVE OXIDATION; VPO CATALYSTS; HYDROGEN PHOSPHATE; IN-SITU; TRANSFORMATION; ACTIVATION; VOPO4-CENTER-DOT-2H(2)O;
D O I
10.1016/j.cej.2009.07.055
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this paper, we have developed a simple, low-cost, template-free and surfactant-free solvothermal process for synthesis of vanadyl hydrogen phosphate hemihydrate (VOHPO(4)center dot 0.5H(2)O) with well defined crystal size. The synthesis was performed by reaction of VPO(4)center dot 2H(2)O with an aliphatic alcohol (isobutyl alcohol, 1-pentanol, 1-hexanol, 1-heptanol or 1-decanol). This afforded well crystallized VOHPO(4)center dot 0.5H(2)O by solvothermal methods at 120 degrees C temperature. This new method significantly reduced the preparation time and lowered production temperature (50%) of catalyst precursor (VOHPO(4)center dot 0.5H(2)O) when compared to conventional hydrothermal synthesis methods. By varying the reducing agent, the solvothermal evolution process from layered tetragonal phase VOPO(4)center dot 2H(2)O to orthorhombic phase VOHPO(4)center dot 0.5H(2)O was observed. It was found that the length of carbon chain in an alcohol in the solvothermal condition had a great impact on chemical and physical properties of resulting catalysts. Interestingly, there was no trace of VO(H(2)PO(4))(2) an impurity noted to be readily formed under solvothermal preparation condition. Therefore, this study introduces a more facile synthetic pathway to V(III) compounds. In addition, the microwave-synthesized catalysts exhibited some properties superior to those of conventionally synthesized catalyst such as better stability, crystallinity, and catalytic activity in the production of maleic anhydride. The characterization of both precursors and calcined catalysts was carried out using X-ray diffraction (XRD), inductively coupled plasma-atomic emission spectrometer (ICP-AES), N(2) physisorption, temperature programmed reduction (H(2)-TPR) and scanning electron microscopy (SEM). The XRD pattern of the active catalyst prepared by this solvothermal method confirmed the presence of smaller crystal size (between 6 and 13 nm along 0 2 0 planes) of vanadium phosphate catalyst with higher specific surface area. Finally, the yield of maleic anhydride was significantly increased from 29% for conventional catalyst to 44% for the new solvothermal catalyst. Crown Copyright (C) 2009 Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:514 / 522
页数:9
相关论文
共 45 条
[1]   EVOLUTION OF A VPO CATALYST IN N-BUTANE OXIDATION REACTION DURING THE ACTIVATION TIME [J].
ABON, M ;
BERE, KE ;
TUEL, A ;
DELICHERE, P .
JOURNAL OF CATALYSIS, 1995, 156 (01) :28-36
[2]   Correlation with the redox V5+/V4+ ratio in vanadium phosphorus oxide catalysts for mild oxidation of n-butane to maleic anhydride [J].
Abon, M ;
Herrmann, JM ;
Volta, JC .
CATALYSIS TODAY, 2001, 71 (1-2) :121-128
[3]   Key aspects of catalyst design for the selective oxidation of paraffins [J].
Albonetti, S ;
Cavani, F ;
Trifiro, F .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1996, 38 (04) :413-438
[4]   A comparison of the reactivity of ''nonequilibrated'' and ''equilibrated'' V-P-O catalysts: Structural evolution, surface characterization, and reactivity in the selective oxidation of n-butane and n-pentane [J].
Albonetti, S ;
Cavani, F ;
Trifiro, F ;
Venturoli, P ;
Calestani, G ;
Granados, ML ;
Fierro, JLG .
JOURNAL OF CATALYSIS, 1996, 160 (01) :52-64
[5]   A solvothermal synthesis and the structure of K4Ag2Sn3S9•2KOH [J].
An, YL ;
Ji, M ;
Baiyin, M ;
Liu, X ;
Jia, CY ;
Wang, DH .
INORGANIC CHEMISTRY, 2003, 42 (14) :4248-4249
[6]   SYNTHESIS AND CHARACTERIZATION OF NEW VPO CATALYSTS FOR PARTIAL NORMAL-BUTANE OXIDATION TO MALEIC-ANHYDRIDE [J].
BATIS, NH ;
BATIS, H ;
GHORBEL, A ;
VEDRINE, JC ;
VOLTA, JC .
JOURNAL OF CATALYSIS, 1991, 128 (01) :248-263
[7]   A solvothermal route to high-surface-area nanostructured MoS2 [J].
Berntsen, N ;
Gutjahr, T ;
Loeffler, L ;
Gomm, JR ;
Seshadri, R ;
Tremel, W .
CHEMISTRY OF MATERIALS, 2003, 15 (23) :4498-4502
[8]   VANADYL PYROPHOSPHATE - A CRITICAL OVERVIEW [J].
CENTI, G .
CATALYSIS TODAY, 1993, 16 (01) :5-26
[9]   MECHANISTIC ASPECTS OF MALEIC-ANHYDRIDE SYNTHESIS FROM C4-HYDROCARBONS OVER PHOSPHORUS VANADIUM-OXIDE [J].
CENTI, G ;
TRIFIRO, F ;
EBNER, JR ;
FRANCHETTI, VM .
CHEMICAL REVIEWS, 1988, 88 (01) :55-80
[10]  
Centi G., 2001, Selective Oxidation by Heterogeneous Catalysis