Heterogeneous catalyst engineering ⇒ from stable and deactivation resistant to viable technical catalyst


Catalysis engineering (HCE)

Heterogeneous catalyst engineering: from stable, deactivation-resistant active phases to viable technical catalysts. We design catalysts that remain active under industrial conditions and can be manufactured at scale, from the active site to the shaped particle. Stability, scalability, and transport inside the particle are design targets from the start, not properties checked at the end. We work on thermal, photothermal, electro- and bioelectrochemical catalysts.

Problem statement. Changes in the structure of a heterogeneous catalyst are made to improve its function: activity, selectivity,y and stability. Linking structure and function requires synthesis protocols that control surface properties and porosity, identification of the active sites, mechanisms, and computational analysis.

Advances in materials science produce more active catalysts. A more active catalyst is usually more prone to deactivation and more likely to be limited by mass and heat transfer. Many advanced catalysts do not reach application because their stability under industrial conditions, with impurities, and the scale-up of their formulation were not part of the design.

The active phase also cannot be used directly in a reactor. Mechanical strength, heat and mass transport, rt and fluidization behavior require mixing it with binder and filler and shaping it into a technical catalyst [201].

Our approach, scale by scale. Our catalysts should (i) keep their stability under industrial conditions, (ii) be scalable with earth-abundant elements, and (iii) connect atomic design with reactor performance. The video zooms from the plant into a single active site, and each paragraph below matches one scene.

1. Process: activity over months. Industrial reactors run for months with heat, pressure, and impurities such as sulfur, chlorine, aromatics, and water. A catalyst has to remain active over that time, not only on day one. Stability under these conditions is the criterion we use to select formulations.

2. Reactor: the catalyst is a shaped body. Inside the reactor, the catalyst is an extrudate in a packed bed or a microsphere in a fluidized bed. The shape sets pressure drop, attrition, heat transfer, and access of reactants to the active phase [201].

3. Particle: the technical catalyst. A technical catalyst combines the active phase with binder, filler and, in our case, silicon carbide (SiC) [131] . SiC conducts heat out of the particle in exothermic reactions such as oxidative coupling of methane [113, 121] and into it in endothermic reforming, where it also reduces coking [132, 144] . We shape particles by:

  • spray drying and extrusion [113, 144] ;
  • spray fluidized bed, for particles of 100 to 200 µm, a size range other methods do not cover well [164, 188, 204] ;
  • electrospinning.

4. Crystal: confinement of the active sites. We support and encapsulate active sites in hosts that limit sintering and coke growth:

  • zeolites, including hierarchical and hollow ZSM-5 with framework-bound or encapsulated Ni for ethylene oligomerization [122, 151, 198, 208] and modified Zn/ZSM-5 for methanol to aromatics [169, 202] ;
  • metal-organic frameworks, with Cu and Pd encapsulated in ZIF-8 that remain stable in CO2 hydrogenation [163, 178, 182] , and MOFs used as precursors of Cu-Zn alloys [210] ;
  • exsolved perovskites for dry reforming of methane and crude oil reforming [136, 166, 183] ;
  • MXenes and graphene for electro-, photo- and bioelectrochemical systems [133, 135, 174, 192, 199, 207] .

5. Active site: alloys and interfaces. At the nanoscale, alloys and interfaces set the binding strength of reactants and intermediates. Examples are Ni-Fe, Ni-Zn, Ni-Ti and high-entropy alloys for dry reforming, where carbon must be removed before it grows [136, 150, 157, 205] , Cu-Ga and Cu-Zn for CO2 hydrogenation [127, 191, 210] , and metal sulfides for H2S decomposition to H2 [180] . Stability is a design target, verified under industrial conditions.

Goals. Our goals are grouped into these lines of work:

  • Technical catalyst I: spray drying and extrusion, with formulation (binder, filler, SiC) linked to activity, stability, heat transfer, and strength.
  • Technical catalyst II: spray fluidized bed granulation and coating, aggregation kinetics, and layered particles for fluidized and circulating reactors.
  • Technical catalyst III: electrospinning.
  • Zeolite catalysts with defined structure and porosity, including hierarchical and hollow zeolites with encapsulated metals.
  • Multi-metal and high-entropy alloy catalysts.
  • MXene catalysts, single- and multi-dimensional, for electro- and bioelectrochemical reactors.
  • Perovskite catalysts, including exsolved metal nanoparticles.
  • Metal-organic framework catalysts with encapsulated metal sites.
  • Supported metal and metal-oxide catalysts.
  • Aerogel catalysts.

Applications. We apply this competency to:

  • CO2 hydrogenation to methanol and sustainable aviation fuel, and scale-up of Cu/ZIF-8.
  • Dry reforming and reforming of methane and crude oil to H2.
  • H2S decomposition to H2 and sulfur.
  • Methanol to hydrocarbons, oligomerization and alkylation to jet fuel.
  • Electrodes for CO2 reduction, microbial fuel cells, and microbial electrolysis cells.

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Engineering Catalysts at the Multiscale: Past, Present, and Future of Catalyst Manufacturing and Shaping Processes

by Alkadhem, Perez-Botella, Pietsch-Braune, Mohamed, Grande, Heinrich, Castaño
ChemCatChem Year: 2026 DOI: https://doi.org/10.1002/cctc.202501109

Abstract

Catalyst shaping is pivotal in optimizing catalytic performance across industrial chemical processes. The engineering of catalysts at multiple scales, ranging from nano to macro, has considerably evolved over the years, driven by advancements in shaping technology. We explore the progression of catalyst shaping, beginning with traditional methods, such as pelletizing and granulation, and advancing to modern techniques, including extrusion, spray-drying, fluidized-bed processes, and additive manufacturing (AM). This work emphasizes shaping technology tailored to specific reactor types, such as fixed-bed (up to structured catalyst) and fluidized-bed reactors. We highlight critical parameters to optimize and control catalyst properties and their direct influence on enhancing catalyst durability, activity, and selectivity. Advances in computational modeling, including multiscale simulations and machine learning-driven design, have further revolutionized catalyst shaping by enabling precise control and accelerating innovation. This review offers a comprehensive perspective on the future of multiscale catalyst shaping and underscores its potential to drive enhanced catalytic performance and sustainable chemical processes by analyzing historical developments, current trends, and emerging technology.

Keywords

CRE HCE