Synthesis of linear alkyl benzenes over zirconia-supported 12-molybdophosphoric acid catalysts

被引:24
作者
Devassy, BM
Lefebvre, F
Böhringer, W
Fletcher, J
Halligudi, SB [1 ]
机构
[1] Natl Chem Lab, Inorgan Chem & Catalysis Div, Pune 411008, Maharashtra, India
[2] CNRS, CPE, Lab Chim Organomet Surface, Villeurbanne, France
[3] Univ Cape Town, Dept Chem Engn, ZA-7701 Rondebosch, South Africa
关键词
zirconia; 12-molybdophosphoric acid; linear alkyl benzene; benzene alkylation;
D O I
10.1016/j.molcata.2005.03.033
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
The liquid-phase alkylation of benzene with 1-octene and 1-dodecene was investigated using zirconia-supported 12-molybdophosphoric acid (MPA) as catalyst. The catalysts with different MPA loading (5-25 wt.% calcined at 700 degrees C) and calcination temperature (15 wt.% calcined from 500 to 750 degrees C) were prepared by suspending zirconium oxyhydroxide in methanol solution of MPA followed by drying and calcination. These catalysts were characterized by X-ray diffraction, and P-31 MAS NMR spectroscopy measurements. The XRD results indicated that MPA stabilizes the tetragonal phase of zirconia. 3 1 P MAS NMR spectra show that the nature of phosphorous species depend on MPA loading and calcination temperature, and it show the existence of three types of phosphorous species, one is the Keggin unit and the other is the decomposition product of MPA and third one an unidentified species. FTIR pyridine adsorption on 15% MPA catalyst calcined at 700 degrees C showed the presence both Bronsted and Lewis acidity. Under the reaction conditions of 83 C, benzene/1-olefin molar ratio of 10 (time, 1 h), the most active catalyst, 15% MPA calcined at 700 C gave more than 90% olefin conversion with selectivity to 2-phenyl octane, 55% and 2-phenyl dodecane, 45%. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 167
页数:6
相关论文
共 33 条
[21]   The acidity and catalytic activity of supported acidic cesium dodecatungstophosphates studied by MAS NMR, FTIR, and catalytic test reactions [J].
Molnár, A ;
Beregszászi, T ;
Fudala, A ;
Lentz, R ;
Nagy, JB ;
Kónya, Z ;
Kiricsi, I .
JOURNAL OF CATALYSIS, 2001, 202 (02) :379-386
[22]   SURFACE-ACIDITY OF ETA-ALUMINA .1. PYRIDINE CHEMISORPTION AT ROOM-TEMPERATURE [J].
MORTERRA, C ;
CHIORINO, A ;
GHIOTTI, G ;
GARRONE, E .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1979, 75 :271-288
[23]  
Okuhara T, 1996, ADV CATAL, V41, P113, DOI 10.1016/S0360-0564(08)60041-3
[24]  
Pope M.T., 1983, HETEROPOLY ISOPOLY O
[25]   Silica-supported 12-molybdophosphoric acid catalysts: Influence of the thermal treatments and of the Mo contents on their behavior, from IR, Raman, X-ray diffraction studies, and catalytic reactivity in the methanol oxidation [J].
RocchiccioliDeltcheff, C ;
Aouissi, A ;
Launay, S ;
Fournier, M .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1996, 114 (1-3) :331-342
[26]   ALKYLATION OF BENZENE WITH DODECENE-1 CATALYZED BY SUPPORTED SILICOTUNGSTIC ACID [J].
SEBULSKY, RT ;
HENKE, AM .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1971, 10 (02) :272-&
[27]   DISTRIBUTION OF ISOMERS IN THE ALKYLATION OF BENZENE WITH LONG-CHAIN OLEFINS OVER SOLID ACID CATALYSTS [J].
SIVASANKER, S ;
THANGARAJ, A .
JOURNAL OF CATALYSIS, 1992, 138 (01) :386-390
[28]   ACID-BASE BIFUNCTIONAL CATALYSIS BY ZRO2 AND ITS MIXED OXIDES [J].
TANABE, K ;
YAMAGUCHI, T .
CATALYSIS TODAY, 1994, 20 (02) :185-198
[29]   SURFACE AND CATALYTIC PROPERTIES OF ZRO2 [J].
TANABE, K .
MATERIALS CHEMISTRY AND PHYSICS, 1985, 13 (3-4) :347-364
[30]  
TEJERO JLB, 1992, Patent No. 5146026