4.7 Article

Low-temperature hydrolysis of carbonyl sulfide in blast furnace gas using Al2O3-based catalysts with high oxidation resistance

Journal

FUEL
Volume 310, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.122295

Keywords

Blast furnace; Alumina-based catalysts; COS; Sulfate deposition; High oxidation resistance

Funding

  1. National Natural Science Foundation of China [51868030, 52070090, 52100122]
  2. Science and Technology Planning Project of Yunnan Province [202001AU070031]
  3. National Key Research and Development Program of China [2018YFC0213400, 2017YFC210500]

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The study investigated the hydrolysis and deactivation mechanisms of catalysts synthesized by depositing K2O and MoO3 on industrial alumina-based catalysts, finding that this modification substantially enhanced COS hydrolysis activity and reduced lattice oxygen content. The introduction of K2O and MoO3 increased weakly basic sites on the catalysts. The modified catalysts showed high oxidation resistance and hydrolysis properties, making them potentially useful in the manufacturing industry.
Water vapor, O-2 and various sulfides in blast furnace gases affect the carbonyl sulfide (COS) hydrolysis reaction. In this study, we investigated the hydrolysis and deactivation mechanisms of a series of catalysts that were synthesized by depositing K2O and MoO3 on industrial alumina-based catalysts. Alumina nanosheets were deposited with potassium oxide, in which MoO3 nanoparticles were incorporated resulting in needle-like structures. The modified catalysts had substantially enhanced COS hydrolysis activity at low temperatures. The introduction of K2O and MoO3 significantly increased the number of weakly basic sites on the catalysts and reduced the lattice oxygen content. The catalysts exhibited high oxidation resistance and hydrolysis properties. According to the poisoning mechanism, the deposition of sulfate species tended to reduce weakly basic sites. High-valent Mo easily excited the adsorbed H2O on the catalysts, producing -OH groups that facilitated the COS hydrolysis reaction. This modification facilitates the further investigation of catalysts capable of promoting COS hydrolysis and their application in the manufacturing industry.

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