Nickel-calcium phosphate/hydroxyapatite catalysts for partial oxidation of methane to syngas: characterization and activation

被引:66
作者
Jun, JH
Lee, TJ
Lim, TH
Nam, SW
Hong, SA
Yoon, KJ [1 ]
机构
[1] Sungkyunkwan Univ, Dept Chem Engn, Suwon 440746, South Korea
[2] Yeungnam Univ, Sch Chem Engn & Technol, Kyongsan 712749, South Korea
[3] Korea Inst Sci & Technol, Battery & Fuel Cell Res Ctr, Seoul 136791, South Korea
关键词
nickel; partial oxidation of methane; calcium hydroxyapatite; calcium phosphate; syngas;
D O I
10.1016/j.jcat.2003.07.004
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
Nickel-calcium phosphate/hydroxyapatite catalysts exhibited high activity and selectivity in the partial oxidation of methane (POM). Characterizations have been performed in order to understand the characteristics of these catalysts. TEM showed that very fine, needle-shaped nickel particles of a few nanometers were present in the sample after the reaction. TPR showed the presence of three nickel species in the fresh (before-reaction) sample, confirming that the nickel in the calcium hydroxyapatite and phosphate structures comes out as fine particles and is reduced during the reaction. The crystalline phases observed were calcium phosphate, calcium hydroxyapatite, NiO, and metallic Ni. As the Ca/PO4 ratio increased, the calcium hydroxyapatite phase tended to increase over the calcium phosphate phase. As the Ni/PO4 ratio increased, the amount of NiO increased in the fresh samples and the amount of metallic Ni also increased in the used (after-reaction) catalysts with the decrease of the NiO. The catalytically active component is certainly the metallic nickel that is produced under reducing environment during the reaction, but its surface is totally reoxidized at 673 K and loses the activity completely. The catalyst could be activated by the reactants only, without the H-2 pretreatment. The first activation could be achieved at 923 K or below, and the subsequent activation at 723 K. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:178 / 190
页数:13
相关论文
共 24 条
[1]   Mechanistic studies of methane partial oxidation to syngas over SiO2-supported rhodium catalysts [J].
Au, CT ;
Wang, HY .
JOURNAL OF CATALYSIS, 1997, 167 (02) :337-345
[2]   Synthesis and characterization of new strontium iron (II) phosphates, SrFe2 (PO4)2 and Sr9Fe1.5 (PO4)7 [J].
Belik, AA ;
Lazoryak, BI ;
Pokholok, KV ;
Terekhina, TP ;
Leonidov, IA ;
Mitberg, EB ;
Karelina, VV ;
Kellerman, DG .
JOURNAL OF SOLID STATE CHEMISTRY, 2001, 162 (01) :113-121
[3]  
BRIGGS D, 1990, PRACTICAL SURFACE AN, V1
[4]  
CHEN Y, 2000, STUD SURF SCI CATAL, V130, P2543
[5]   Oxidative conversion of methane to syngas over nickel supported on commercial low surface area porous catalyst carriers precoated with alkaline and rare earth oxides [J].
Choudhary, VR ;
Uphade, BS ;
Mamman, AS .
JOURNAL OF CATALYSIS, 1997, 172 (02) :281-293
[6]   NONEQUILIBRIUM OXIDATIVE CONVERSION OF METHANE TO CO AND H-2 WITH HIGH SELECTIVITY AND PRODUCTIVITY OVER NI/AL2O3 AT LOW-TEMPERATURES [J].
CHOUDHARY, VR ;
RAJPUT, AM ;
PRABHAKAR, B .
JOURNAL OF CATALYSIS, 1993, 139 (01) :326-328
[7]  
Cullity B.D., 1978, Addison-Wesley Series in Metallurgy and Materials, Vsecond
[8]  
Diskin A. M., 2000, STUD SURF SCI CATAL, V130, P3519
[9]   ARE THE EQUILIBRIUM CONCENTRATIONS OF CO AND H-2 EXCEEDED DURING THE OXIDATION OF CH4 OVER A NI/YB2O3 CATALYST [J].
DISSANAYAKE, D ;
ROSYNEK, MP ;
LUNSFORD, JH .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (15) :3644-3646
[10]   PARTIAL OXIDATION OF METHANE TO CARBON-MONOXIDE AND HYDROGEN OVER A NI/AL2O3 CATALYST [J].
DISSANAYAKE, D ;
ROSYNEK, MP ;
KHARAS, KCC ;
LUNSFORD, JH .
JOURNAL OF CATALYSIS, 1991, 132 (01) :117-127