Volume 47 Issue 3
Mar.  2019
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HAN Lei, HUANG Chuan-feng, LIU Shu-wei, CHENG Qiu-xiang, CHANG Fang-yuan. Investigation of performance of Ni/W-USY/Al2O3 catalyst with full mesoporous in Fischer Tropsch wax hydrocracking[J]. Journal of Fuel Chemistry and Technology, 2019, 47(3): 329-337.
Citation: HAN Lei, HUANG Chuan-feng, LIU Shu-wei, CHENG Qiu-xiang, CHANG Fang-yuan. Investigation of performance of Ni/W-USY/Al2O3 catalyst with full mesoporous in Fischer Tropsch wax hydrocracking[J]. Journal of Fuel Chemistry and Technology, 2019, 47(3): 329-337.

Investigation of performance of Ni/W-USY/Al2O3 catalyst with full mesoporous in Fischer Tropsch wax hydrocracking

Funds:

The project was supported by National Science and Technology Major Project 2018YFB0604600

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  • Corresponding author: HUANG Chuan-feng, Tel: 15009297336, E-mail: huangcf1130@163.com
  • Received Date: 2018-10-29
  • Rev Recd Date: 2019-01-14
  • Available Online: 2021-01-23
  • Publish Date: 2019-03-10
  • Ni/W-USY/Al2O3 with full mesoporous structure was prepared and used for hydrocracking of Fischer Fropsch wax. The catalyst was evaluated for its reaction performance, product characteristics and catalyst properties change. In a 312 h experiment, the result showed that the catalyst possessed high initial activity, and maintained stable after 120 h, and did not show obvious deactivation afterward. When the heavy wax conversion reached 73.95% at the stable stage, the fuel oil selectivity reached to 98.46% and C3, 4 constituted the most cracked gas. Gasoline, kerosene and diesel, as the products, were transparent and composed of paraffins and iso-paraffins substituted by methyl-groups. The iso-paraffin contents in the three products were 63.98%, 52.26% and 48.90% respectively. The fresh catalyst contained two main active states of WS2 and NiWS, had good metal dispersion and rich mesoporous structure. With transition from high activity to stable state of the catalyst property, part of W migrated and formed more Ni-S-W bonds with Ni, and some W-S bonds broke to form W-W bonds after releasing S, resulting in the increase of active states of NiWS and the decrease of WS2, and forming more Brönsted acid sites and less Lewis acid sites.
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