TY - JOUR A1 - Anton, Johan A1 - Ruland, Holger A1 - Kaluza, Stefan A1 - Muhler, Martin T1 - Fast and Reproducible Testing of Cu–Co-Based Catalysts Applied in the Conversion of Synthesis Gas to Ethanol and Higher Alcohols JF - Catalysis Letters Y1 - 2015 U6 - https://doi.org/10.1007/s10562-015-1543-2 N1 - The work was part of the project “Bioethanol from synthesis gas—BETSY”, funded by the Ministry for Economy, Energy, Building, Habitation and Transportation of Northrhine-Westphalia within the program Ziel2.NRW financed by the European Union through the European regional development fund ERDF. VL - 145 IS - 7 SP - 1374 EP - 1381 PB - Springer ER - TY - JOUR A1 - Bordoloi, Ankur A1 - Sanchez, Miguel A1 - Noei, Heshmat A1 - Kaluza, Stefan A1 - Großmann, Dennis A1 - Wang, Yuemin A1 - Grünert, Wolfgang A1 - Muhler, Martin T1 - Catalytic Behaviour of Mesoporous Cobalt-Aluminum Oxides for CO Oxidation JF - Journal of Catalysts Y1 - 2014 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:hbz:due62-opus-34344 SN - 2314-5110 SP - 1 EP - 9 PB - Hindawi ER - TY - JOUR A1 - Boz, İsmail A1 - Kaluza, Stefan A1 - Boroğlu, Mehtap Şafak A1 - Muhler, Martin T1 - Synthesis of high surface area ZnO powder by continuous precipitation JF - Materials Research Bulletin Y1 - 2012 U6 - https://doi.org/10.1016/j.materresbull.2012.02.005 SN - 1873-4227 VL - 47 IS - 5 SP - 1185 EP - 1190 PB - Elsevier ER - TY - JOUR A1 - Heeskens, Denise A1 - Aghaei, Pedram A1 - Kaluza, Stefan A1 - Strunk, Jennifer A1 - Muhler, Martin T1 - Selective oxidation of ethanol in the liquid phase over Au/TiO 2 JF - physica status solidi (b) Y1 - 2013 U6 - https://doi.org/10.1002/pssb.201248440 SN - 1521-3951 VL - 250 IS - 6 SP - 1107 EP - 1118 PB - Wiley ER - TY - JOUR A1 - Kaluza, Stefan A1 - Behrens, Malte A1 - Schiefenhövel, Nora A1 - Kniep, Benjamin A1 - Fischer, Richard A1 - Schlögl, Robert A1 - Muhler, Martin T1 - A Novel Synthesis Route for Cu/ZnO/Al2O3 Catalysts used in Methanol Synthesis: Combining Continuous Consecutive Precipitation with Continuous Aging of the Precipitate JF - ChemCatChem Y1 - 2011 U6 - https://doi.org/10.1002/cctc.201000329 SN - 1867-3899 VL - 3 IS - 1 SP - 189 EP - 199 PB - Wiley ER - TY - JOUR A1 - Kaluza, Stefan A1 - Muhler, Martin T1 - On the precipitation mechanism and the role of the post-precipitation steps during the synthesis of binary ZnO–Al2O3 composites with high specific surface area JF - Journal of Materials Chemistry KW - FBMV Y1 - 2009 U6 - https://doi.org/10.1039/b902004g SN - 1364-5501 VL - 19 IS - 23 SP - 3914 EP - 3922 PB - Royal Society of Chemistry (RSC) ER - TY - JOUR A1 - Kaluza, Stefan A1 - Muhler, Martin T1 - On the Role of Aging, Washing, and Drying in the Synthesis of Polycrystalline Zinc Oxide by Precipitation: Combining Fast Continuous Mixing, Spray Drying and Freeze Drying to Unravel the Solid-State Transformations of the Precipitate JF - Catalysis Letters Y1 - 2009 UR - 1572-879X U6 - https://doi.org/10.1007/s10562-008-9818-5 N1 - The authors gratefully acknowledge fruitful discussions with Malte Behrens and Robert Schlögl, and the financial support by the BMBF (Bundesministerium für Bildung und Forschung) within the scope of the project 01RI05028 “Entwicklung von Methanolsynthesekatalysatoren als Basis für nachhaltige Ressourcennutzung” VL - 129 IS - 3-4 SP - 287 EP - 292 PB - Springer ER - TY - JOUR A1 - Winter, Franziska Luise A1 - Diehl, Patrick A1 - Telaar, Pascal A1 - Watermann, Clara Maria A1 - Kaluza, Stefan A1 - Muhler, Martin A1 - Apfel, Ulf-Peter A1 - Zeidler-Fandrich, Barbara T1 - Influence of the catalyst precursor for cobalt on activated carbon applied in ammonia decomposition JF - Catalysis Today N2 - Ammonia is a key compound for storing and transporting green hydrogen. However, the efficient release of stored hydrogen through thermocatalytic ammonia decomposition is achievable only at temperatures around 600 °C, particularly with non-noble metal-based catalysts, which prove to be both ecologically and economically more feasible. In this study, electrically conductive activated carbon was selected as the catalyst support, chosen specifically for its suitability in achieving more energy-efficient direct reactor heating through the ohmic resistance of the catalysts. Cobalt salts were wet impregnated on activated carbon investigating the influence of different precursors (cobalt nitrate and cobalt acetate) and pyrolysis temperatures (400 °C and 600 °C) under N2 flow on the cobalt particle size and the incorporation of cobalt into the carbon matrix. TEM imaging and CO-chemisorption revealed well dispersed cobalt particles with sizes below 10 nm for the catalysts synthesized from the cobalt nitrate precursor. On the other hand, cobalt acetate led to about nine times larger Co agglomerates, which were partially detached from the carbon matrix. Moreover, this substantial difference in the Co particle size results in a significantly higher ammonia conversion for cobalt nitrate-based catalysts, achieving 94 % of ammonia conversion at 600 °C. Furthermore, the long-term stability test of the cobalt nitrate-based catalyst resulted in a slight deactivation of only 2 % ammonia conversion at 500 °C. KW - Katalyse KW - Ammoniak KW - Grüner Wasserstoff KW - Ammonia decomposition KW - Carbon supported cobalt KW - Synthesis design KW - Cobalt acetate KW - Cobalt nitrate KW - Resistance heating Y1 - 2024 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:hbz:due62-opus-46600 SN - 0920-5861 VL - 429 PB - Elsevier ER -