Skip to main content
. 2026 Aug 12;16(39):43391–43413. doi: 10.1039/d6ra01860b

Table 4. Overview of hydrogenation process using common LOHC candidates concerning catalyst types, reactor configurations, kinetics and performance.

LOHC system Typical catalyst (s) Reactor configuration Operating conditions Kinetic characteristics Advantages Limitations Ref.
Toluene to methylcyclohexane (MCH) Noble metals (Pt, Pd, Ru) on oxide supports Fixed-bed/trickle-bed (gas-liquid-solid) 185–225 °C; 0.3–2 MPa Fast hydrogenation kinetics; activation energy ≈ 35–50 kJ mol−1, depending on the catalyst; equilibrium-limited at high conversion Mature chemistry; good logistics compatibility; fast hydrogenation kinetics Catalyst cost: heat removal needed (exothermic); overall system limited by dehydrogenation step 75–78
Dibenzyltoluene (DBT) to Perhydro-DBT (H18-DBT) Mainly Ru-based and Pt/Pd catalysts (supported) Fixed bed; continuous flow systems 120–250 °C; 30–50 bar Activation energy ≈ 45–60 kJ mol−1; reaction often limited by heat and mass transfer due to high viscosity DBT is low-volatility and stable, attractive for large-scale storage logistics Viscosity/mass transfer constraints; concerns with catalyst deactivation; hydrogenation heat management 46 and 79
Enthalphy: −65.4 kJ molH2−1
N-ethylcarbazole (NEC) to 12H-NEC Mainly Ru, also Pt/Pd, depending on design Fixed-bed and batch screening reactors Temperature: 130–180 °C and pressure 50–80 bar Activation energy ≈ 30 to 70 kJ mol−1 High hydrogen capacity class; potentially lower energy requirement for dehydrogenation vs. hydrocarbons Carrier/catalyst sensitivity; possible by-product formation; careful purity control needed 80 and 81
Enthaplhy: −50 kJ molH2−1
Hydrogenation of LOHCs Noble metals are dominant; Ni-based materials are explored as a lower-cost alternative Trickle-bed/slurry/fixed-bed Conditions tuned by carrier and catalyst Strong industrial knowledge base from refinery hydrogenation; scalable reactor choices Non-noble catalysts may show lower activity or stability; long-term cycling is critical 11, 82 and 83
Hydrogenation process design Catalyst choice depends on heat removal, selectivity, and stability Heat-integrated fixed-bed and process loops Exothermic heat must be controlled Hydrogenation heat can be recovered for system efficiency Hotspots can accelerate deactivation; scale-up requires thermal control and gas–liquid mass transfer optimisation 84–88