A Study of the Fischer–Tropsch Synthesis in a Batch Reactor: Rate, Phase of Water, and Catalyst Oxidation
Xiaojun Lu, Xiaowei Zhu, Cornelius Mduduzi Masuku, Diane Hildebrandt, David Glasser
Abstract
Xiaojun Lu, Xiaowei Zhu, Cornelius Mduduzi Masuku, Diane Hildebrandt, David Glasser
Abstract
We used a batch reactor to conduct the Fischer–Tropsch reaction on a Co/TiO 2 catalyst without charging any liquid in the reactor tank. The catalyst was loaded in a fixed catalyst basket, and the reactor was operated as a “gas–solid” reaction system. Before entering the batch operation for the reactor, it was initially operated under CSTR mode. The reactor was controlled under 210 °C and 20 bar (g) of pressure with a 2:1 H 2 /CO ratio in the feed gas when it was under CSTR mode. The time for the batch operations was varied between 20 min and 22.5 h. After each batch operation, the reactor was resumed to the CSTR mode for building up the same starting conditions for different batch operations. Both the selectivity to the olefinic and paraffinic products and the reaction rate were observed to increase when changing the operation from CSTR to batch mode. The reactor pressure was monitored and the comparison of the reading pressure and the pressure derived from the mass balance suggested that part of the product water was in the liquid phase in the reactor. Oxidation of Co might have happened when approaching the end of the batch operation.
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We used a batch reactor to conduct the Fischer–Tropsch reaction on a Co/TiO 2 catalyst without charging any liquid in the reactor tank. The catalyst was loaded in a fixed catalyst basket, and the reactor was operated as a “gas–solid” reaction system. Before entering the batch operation for the reactor, it was initially operated under CSTR mode. The reactor was controlled under 210 °C and 20 bar (g) of pressure with a 2:1 H 2 /CO ratio in the feed gas when it was under CSTR mode. The time for the batch operations was varied between 20 min and 22.5 h. After each batch operation, the reactor was resumed to the CSTR mode for building up the same starting conditions for different batch operations. Both the selectivity to the olefinic and paraffinic products and the reaction rate were observed to increase when changing the operation from CSTR to batch mode. The reactor pressure was monitored and the comparison of the reading pressure and the pressure derived from the mass balance suggested that part of the product water was in the liquid phase in the reactor. Oxidation of Co might have happened when approaching the end of the batch operation.
Key concepts: Fischer–Tropsch process, Catalysis, Chemical engineering, Phase (matter), Chemistry, Batch reactor, Materials science, Organic chemistry