Welcome to the DFG Collaborative Research Center CRC 1615 SMART Reactors

We are facing the societal challenges of transforming economic and production chains from fossil raw materials to sustainable and renewable raw materials. However, these can fluctuate seasonally and geologically in their availability and quality. Society therefore urgently needs processes and reactors that can respond flexibly to fluctuating raw material properties. To enable such adaptation, a very high level of process control is required: pressures, temperatures, concentrations and dispersed phases must be monitored continuously and in situ in the reactors using suitable sensors.

As part of the Collaborative Research Center, we aim to address this issue and enable SMART reactors through basic research. In the future, the SMART reactors will convert sustainable renewable resources into different products (multi-purpose) in a more sustainable way and operate autonomously (self-adapting), which will lead to more resilient processes that are more transferable between scales and locations.

To achieve our vision, interdisciplinary collaboration between process engineering, materials science and electrical engineering with physicists, chemists, mathematicians and data scientists from Hamburg University of Technology and five research institutions enables the focusing of expertise and unique experimental facilities.

Within the framework of this website, we would like to give you an insight into the individual subprojects, publications related to the CRC, upcoming events and career opportunities within the Collaborative Research Center.

07.06.2024

New publication available online!

Researchers from the groups of Prof. Raimund Horn from the Institute of Chemical Reaction Engineering at the Hamburg University of Technology and Prof. Jakob Albert from the Institute of Technical and Macromolecular Chemistry at the University of Hamburg shared their latest on a compact profile reactor for CO2 hydrogenation.

The compact profile reactor (CPR) design allows for the simultaneous acquisition of species, temperature, and spatially resolved reaction profiles during high-pressure CO2 hydrogenation to methanol. In this study, the reaction profile of In2O3/ZrO2 catalysts is compared to that of the state-of-the-art Cu/ZnO/Al2O3 (CZA) catalyst in a high-pressure CPR. It is demonstrated that the addition of nickel as a promoter significantly enhanced the catalytic activity of pure In2O3/ZrO2. The characterization by H2 TPR and CO2 TPD revealed an increased capacity for both hydrogen and CO2. A detailed comparison and optimization of reaction conditions using Ni–In2O3/ZrO2 as a catalyst are presented. In an optimized experiment, Ni–In2O3/ZrO2 produces 4.90 gMeOH gIn+Ni–1 h–1 at 275 °C, 50 bar, and 63,000 h–1 with a methanol selectivity of 73%. Furthermore, no catalyst deactivation caused by metal leaching or sintering could be observed over 90 h time on stream.

Kampe, P., Herrmann, N., Ruhmlieb, C., Finsel, M., Korup, O., Horn, R., Albert, J. (2024). Spatially Resolved Reaction Profiles of CO2 Hydrogenation to Methanol Using In-Based Catalysts in a Compact Profile Reactor. ACS Sustainable Chemistry & Engineering. 12. (25), 9541−9549.

pubs.acs.org/doi/10.1021/acssuschemeng.4c03279

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