Hydrogen production via the decomposition of hydrogen sulfide is a promising process that enables the simultaneous abatement of a pollutant species, H2S, and the sustainable production of a high-value product, H2. Molybdenum disulfide has emerged as one of the most effective catalysts in enhancing this conversion. However, a detailed understanding of the reaction kinetics is still missing in the literature. In this work, the splitting of H2S over MoS2 was investigated in a tubular reactor at temperatures between 640 and 929 degrees C. A kinetic analysis was performed based on the newly collected data. A first model was developed using a power-law relation, which also accounted for the reverse reaction by introducing thermodynamic equilibrium constants. Additionally, a four- step reaction mechanism was proposed, and a rate equation was derived using the Langmuir-Hinshelwood approach. The kinetic parameters for both models were calculated and found to match the values reported in the literature. A comparison with the thermal decomposition of H2S demonstrated the advantages of using MoS2 as a catalyst, particularly at moderate temperatures. The findings of the study establish a solid basis for improving the efficiency of the process and, by providing reliable kinetics, facilitate its integration into industrial applications.
Experimental and kinetic analysis of hydrogen production via hydrogen sulfide catalytic splitting
Nova, Anna;Negri, Francesco;Moioli, Emanuele;Manenti, Flavio
2025-01-01
Abstract
Hydrogen production via the decomposition of hydrogen sulfide is a promising process that enables the simultaneous abatement of a pollutant species, H2S, and the sustainable production of a high-value product, H2. Molybdenum disulfide has emerged as one of the most effective catalysts in enhancing this conversion. However, a detailed understanding of the reaction kinetics is still missing in the literature. In this work, the splitting of H2S over MoS2 was investigated in a tubular reactor at temperatures between 640 and 929 degrees C. A kinetic analysis was performed based on the newly collected data. A first model was developed using a power-law relation, which also accounted for the reverse reaction by introducing thermodynamic equilibrium constants. Additionally, a four- step reaction mechanism was proposed, and a rate equation was derived using the Langmuir-Hinshelwood approach. The kinetic parameters for both models were calculated and found to match the values reported in the literature. A comparison with the thermal decomposition of H2S demonstrated the advantages of using MoS2 as a catalyst, particularly at moderate temperatures. The findings of the study establish a solid basis for improving the efficiency of the process and, by providing reliable kinetics, facilitate its integration into industrial applications.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


