From CO2 to DME: Enhancement through Heteropoly Acids from a Catalyst Screening and Stability Study

Dustin Kubas; Jennifer Maria Beck; Erdogan Kasisari; Timo Schätzler; Anita Becherer; Anna Fischer; Ingo Krossing

doi:10.1021/acsomega.3c00149

From CO₂ to DME: Enhancement through Heteropoly Acids from a Catalyst Screening and Stability Study

ACS Omega. 2023 Apr 21;8(17):15203-15216. doi: 10.1021/acsomega.3c00149. eCollection 2023 May 2.

Authors

Dustin Kubas^{1

2}, Jennifer Maria Beck^{1

2}, Erdogan Kasisari¹, Timo Schätzler¹, Anita Becherer¹, Anna Fischer^{1

2}, Ingo Krossing^{1

2}

Affiliations

¹ Institut für Anorganische und Analytische Chemie, Universität Freiburg, Albertstr. 21, 79104 Freiburg, Germany.
² Freiburger Materialforschungszentrum (FMF), Universität Freiburg, Stefan-Meier-Straße 21, 79104 Freiburg, Germany.

Abstract

The direct synthesis of dimethyl ether (DME) via CO₂ hydrogenation in a single step was studied using an improved class of bifunctional catalysts in a fixed bed reactor (T _R: 210-270 °C; 40 bar; gas hourly space velocity (GHSV) 19,800 NL kg_cat ^-1 h^-1; ratio CO₂/H₂/N₂ 3:9:2). The competitive bifunctional catalysts tested in here consist of a surface-basic copper/zinc oxide/zirconia (CZZ) methanol-producing part and a variable surface-acidic methanol dehydration part and were tested in overall 45 combinations. As dehydration catalysts, zeolites (ferrierite and β-zeolite), alumina, or zirconia were tested alone as well as with a coating of Keggin-type heteropoly acids (HPAs), i.e., silicotungstic or phosphotungstic acid. Two different mixing methods to generate bifunctional catalysts were tested: (i) a single-grain method with intensive intra-particular contact between CZZ and the dehydration catalyst generated by mixing in an agate mortar and (ii) a dual-grain approach relying on physical mixing with low contact. The influence of the catalyst mixing method and HPA loading on catalyst activity and stability was investigated. From these results, a selection of best-performing bifunctional catalysts was investigated in extended measurements (time on stream: 160 h/7 days, T _R: 250 and 270 °C; 40 bar; GHSV 19,800 NL kg_cat ^-1 h^-1; ratio CO₂/H₂/N₂ 3:9:2). Silicotungstic acid-coated bifunctional catalysts showed the highest resilience toward deactivation caused by single-grain preparation and during catalysis. Overall, HPA-coated catalysts showed higher activity and resilience toward deactivation than uncoated counterparts. Dual-grain preparation showed superior performance over single grain. Furthermore, silicotungstic acid coatings with 1 KU nm^-2 (Keggin unit per surface area of carrier) on Al₂O₃ and ZrO₂ as carrier materials showed competitive high activity and stability in extended 7-day measurements compared to pure CZZ. Therefore, HPA coating is found to be a well-suited addition to the CO₂-to-DME catalyst toolbox.