One‐pot Synthesis of Bulk NiMoS Catalysts: Influence of pH and Addition of Pluronic®P123. Hydrodesulfurization of Model Sulfur Molecules Representative of FCC Gasoline

Author:

Courthéoux Laurence1,Hétier Valentin1,Carvalho Alexandre2,Rousseau Julie2,Lacroix‐Desmazes Patrick1,Girard Etienne3,Uzio Denis3,Brunet Sylvette2ORCID,Pradel Annie1

Affiliation:

1. ICGM UMR CNRS 5253 Université de Montpellier, ENSM 1919 Route de Mende 34293 Montpellier Cedex 5 France

2. IC2MP UMR CNRS 7285 4 rue Michel Brunet, TSA 51106 86073 Poitiers Cedex 9 France

3. IFP Energies nouvelles Rond-point de l'échangeur de Solaize, BP 3 69360 Solaize France

Abstract

AbstractThe worldwide continual reinforcement of regulations for the production of cleaner fuels along with the larger demand for energy urge us to develop hydrotreatment sulfide catalysts exhibiting higher activity in hydrodesulfurization reactions and explore innovative synthesis strategies. In this work, a novel one‐pot synthesis method of unsupported NiMoS catalysts in water at ambient pressure and moderate temperature is described. The reaction conditions including pH variations and addition of a copolymer structuring agent were thoroughly investigated. Catalytic performances of the prepared bulk NiMoS catalysts were measured for the hydrodesulfurization of two model sulfur molecules, representative of FCC gasoline. Catalysts prepared at pH 7 without or with polymer exhibited roughly similar activity, resulting however from different characteristics favorable for catalyst efficiency probably compensating one another, i. e. a very high promotion rate for the first one and smaller particles along with larger specific surface area for the second.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference44 articles.

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2. http://transportpolicy.net/index.php?title=Global_Comparison:_Fuels. (accessed 14 September 2022).

3. Advanced Hydrodesulfurization Catalysts: A Review of Design and Synthesis

4. Hydrodesulfurization with classic Co–MoS2 and Ni–MoS2/γ-Al2O3 and new Pt–Pd on mesoporous zeolite catalysts

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