Advanced monometallic and bimetallic catalysts for energy efficient propylene production via propane dehydrogenation pathways–A review

The production of numerous industrial products, including synthetic rubber, paints, coatings, and plastics, depends heavily on propylene. Interest in creative, effective propylene manufacturing is sparked by rising demand. Direct dehydrogenation of propane is a method for generating only propylene while avoiding byproducts. Pt and CrO x catalysts are used in the key petroleum process of C 3 H 8 to C 3 H 6 dehydrogenation. However, they are expensive and ineffective for selecting propylene. Research focuses on new catalysts and supports to increase selectivity, stability, and activity. Exploring single and bimetal catalysts and different supports improves the dehydrogenation process. This review paper summarises recent developments and fundamental principles behind the propane dehydrogenation (PDH) process. The emphasis is on modern technology, catalyst improvements, and novel chemical approaches to manage catalytic structures and avoid deactivation. An in-depth analysis of active sites, reaction pathways, and deactivation mechanisms involving various metals, bimetals, and supports have been discussed in detail. This review highlights emerging trends in catalyst design focused on reducing activation energy barriers and enhancing selectivity for propylene in propane dehydrogenation (PDH). High paraffin conversion requires temperatures between 550–750 °C and low partial pressures, which, while thermodynamically favourable, pose significant challenges. These harsh conditions can cause sintering, loss of active metal dispersion, and coke formation, leading to catalyst deactivation. Consequently, developing thermally stable, coke-resistant catalysts that maintain activity and selectivity under these extreme conditions is crucial for efficient PDH. • Mechanistic, thermodynamic, and kinetic aspects of non-oxidative PDH reactions. • Catalyst deactivation via coke, sintering, metal loss, and structural changes. • Catalyst design based on electronic, geometric, and ensemble site effects. • Monometallic and bimetallic catalysts: synergy, limitations, and performance. • Support effects: acidity, porosity, and nanostructure for catalytic stability.

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Publication Details

Journal
Applied Energy
Published
2025-06-17
DOI
https://doi.org/10.1016/j.apenergy.2025.126285
Citations
7
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
2.72
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article

Advanced monometallic and bimetallic catalysts for energy efficient propylene production via propane dehydrogenation pathways–A review

Imane Ziani, Mariam Ameen, Farooq Sher, Bohong Wang et al.
7 citations
Applied Energy
Catalysis and Oxidation Reactions
2.72
article

Advanced monometallic and bimetallic catalysts for energy efficient propylene production via propane dehydrogenation pathways–A review

Imane Ziani, Mariam Ameen, Farooq Sher, Bohong Wang, Fatima Zafar, Alexander Chupin, Bilal Fareed, Muhammad Kashif Iqbal Khan, Rabia Fatima, Emina Boškailo
article en
7 citations

Abstract

The production of numerous industrial products, including synthetic rubber, paints, coatings, and plastics, depends heavily on propylene. Interest in creative, effective propylene manufacturing is sparked by rising demand. Direct dehydrogenation of propane is a method for generating only propylene while avoiding byproducts. Pt and CrO x catalysts are used in the key petroleum process of C 3 H 8 to C 3 H 6 dehydrogenation. However, they are expensive and ineffective for selecting propylene. Research focuses on new catalysts and supports to increase selectivity, stability, and activity. Exploring single and bimetal catalysts and different supports improves the dehydrogenation process. This review paper summarises recent developments and fundamental principles behind the propane dehydrogenation (PDH) process. The emphasis is on modern technology, catalyst improvements, and novel chemical approaches to manage catalytic structures and avoid deactivation. An in-depth analysis of active sites, reaction pathways, and deactivation mechanisms involving various metals, bimetals, and supports have been discussed in detail. This review highlights emerging trends in catalyst design focused on reducing activation energy barriers and enhancing selectivity for propylene in propane dehydrogenation (PDH). High paraffin conversion requires temperatures between 550–750 °C and low partial pressures, which, while thermodynamically favourable, pose significant challenges. These harsh conditions can cause sintering, loss of active metal dispersion, and coke formation, leading to catalyst deactivation. Consequently, developing thermally stable, coke-resistant catalysts that maintain activity and selectivity under these extreme conditions is crucial for efficient PDH. • Mechanistic, thermodynamic, and kinetic aspects of non-oxidative PDH reactions. • Catalyst deactivation via coke, sintering, metal loss, and structural changes. • Catalyst design based on electronic, geometric, and ensemble site effects. • Monometallic and bimetallic catalysts: synergy, limitations, and performance. • Support effects: acidity, porosity, and nanostructure for catalytic stability.

Applied EnergyVol. 397
Peoples' Friendship University of Russia (RU), Pakistan Institute of Engineering and Applied Sciences (PK), Clarkson University (US), Washington University in St. Louis (US), Zhejiang Ocean University (CN), Mohamed I University (MA), Herzegovina University (BA), RMIT Europe (ES), Nottingham Trent University (GB)
Affordable and clean energy
Openalex Percentile: Top 9%
Catalysis and Oxidation Reactions
2.72
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