High-temperature Fischer-Tropsch synthesis over FeTi mixed oxide model catalysts: Tailoring activity and stability by varying the Ti/Fe ratio

被引:18
作者
Santos, Vera P. [1 ,3 ]
Borges, Liam [1 ]
Sartipi, Sina [1 ]
van der Linden, Bart
Dugulan, A. Iulian [2 ]
Chojecki, Adam [3 ]
Davidian, Thomas [4 ]
Ruitenbeek, Matthijs [4 ]
Meima, Garry R. [3 ,4 ]
Kapteijn, Freek
Makkee, Michiel
Gascon, Jorge [1 ]
机构
[1] Delft Univ Technol, Dept Chem Engn, Catalysis Engn, Van Maasweg 9, NL-2629 HZ Delft, Netherlands
[2] Delft Univ Technol, Appl Sci Fundamental Aspects Mat & Energy, Van Maasweg 9, NL-2629 HZ Delft, Netherlands
[3] Dow Benelux BV, Core R&D, POB 48, NL-4530 AA Terneuzen, Netherlands
[4] Dow Benelux BV, Hydrocarbons R&D, POB 48, NL-4530 AA Terneuzen, Netherlands
关键词
Bulk Fe-based catalysts; Ti/Fe ratio; Pseudobrookite; Fischer-Tropsch; Reduction; Carburization; Deactivation; IRON TITANATE CATALYST; OLEFINS; REDUCTION; XAFS;
D O I
10.1016/j.apcata.2017.01.002
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
A series of Fe-Ti mixed oxide model catalysts containing different Ti/Fe ratios were synthesized and applied as catalysts for the High Temperature Fischer-Tropsch reaction (HTFTS). XRD, H-2-TPR and in situ Mossbauer and XAFS spectroscopy were applied to evaluate the role of Ti on the physical and chemical properties of Fe within the mixed metal oxide. It was observed that the Ti/Fe ratio determines the relative amounts of hematite, pseudobrookiter and anatase in the starting materials. The interplay between these phases is responsible for the HTFTS catalytic performance. Our results demonstrate that the presence of pseudobrookite: i) enhances the dispersion of iron; ii) mediates and controls the reduction and carburization degree during the transformation of Fe (III) species to carbides upon activation, and iii) increases the stability under HTFTS conditions by minimizing the re oxidation of iron carbides. Highest catalytic activity and stability is achieved for the material with Ti/Fe ratio of 1/2.1. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 48
页数:11
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