Catalytic Conversion of Model Tars over Carbon-Supported Ni and Fe

被引:12
作者
Arteaga-Perez, Luis E. [1 ,2 ]
Delgado, Aaron M. [3 ]
Flores, Mauricio [4 ]
Olivera, Patricia [4 ]
Matschuk, Kimberley [5 ]
Hamel, Christian [5 ]
Schulzke, Tim [5 ]
Jimenez, Romel [3 ]
机构
[1] Univ Bio Bio, Chem Engn Sch, Dept Wood Engn, Concepcion 4030000, Chile
[2] Univ Bio Bio, Wood Engn Dept, Grp Nanomat & Catalysts Sustainable Proc NanoCatp, Concepcion 4030000, Chile
[3] Univ Concepcion, Dept Chem Engn, Concepcion 4030000, Chile
[4] Univ Concepcion, Unit Technol Dev, Concepcion 4030000, Chile
[5] Fraunhofer UMSICHT, Inst Environm Safety & Energy Technol, D-46047 Oberhausen, Germany
关键词
activated carbon; tars; catalytic gas upgrading; BIOMASS GASIFICATION GAS; ACTIVATED CARBON; HYDROGEN-PRODUCTION; OXIDE CATALYSTS; FIXED-BED; HOT-GAS; IRON; PYROLYSIS; CHAR; CRACKING;
D O I
10.3390/catal8030119
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
Tar removal from gasification gases is a determinant step to guarantee the operational feasibility of gasification-to-chemicals/energy systems. This study aimed to develop novel carbon-supported catalysts for the elimination of tarry aromatics (toluene, naphthalene and benzene) from gasification gases. Effects of reaction temperature (700 < T < 900 degrees C) and catalyst nature (Fe-0 and Ni-0) on the activity were assessed by considering thermo-catalytic conversion and steam reforming, under a simulated gasification gas. The catalysts (Ni and Fe) and support (AC) were characterized by X-ray diffraction (XRD), N-2 physisorption, thermogravimetric analysis (TGA), transmission electron microscopy (TEM) and compositional analyses. Both catalysts and support, presented a mesoporous-like texture with a considerable high surface area (690 < S-BET < 743 m(2)/g). Furthermore, dispersion of the metal nanoparticles (active phase) was uniform as confirmed by TEM images. Results from activity tests suggest that Ni/AC has higher effectivity for converting tars than Fe/AC, as confirmed by the low apparent activation energies (34 < E-app < 98 kJ/mol) for naphthalene and benzene conversion between 700 and 900 degrees C. The conversion was 100% above 850 degrees C; nevertheless; below 750 degrees C, a sharp reduction in benzene conversion was observed, which was attributed to reversible carbon deposition.
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页数:18
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