Exceeding Single‐Pass Equilibrium with Integrated Absorption Separation for Ammonia Synthesis Using Renewable Energy—Redefining the Haber‐Bosch Loop
Collin Smith, Laura Torrente‐Murciano
Abstract
Abstract The synthesis of ammonia through the Haber‐Bosch process has been at the foundation of the chemical industry for over 100 years, but when the energy and feedstock sources switch from fossil fuels to renewable electricity, the process needs to be reimagined. Herein, the successful integration of ammonia synthesis and separation is demonstrated in a recycle‐less process setting the foundations of green ammonia technology. The ruthenium‐based catalyst uses a nanostructured CeO 2 support and Cs electronic promotion to remove hydrogen and ammonia inhibition, respectively, creating a catalyst with low‐temperature (<300 °C) activity that quickly approaches equilibrium. The absorbent uses MnCl 2 to avoid the acid releasing decomposition of conventional absorbents like MgCl 2 , and a support of SiO 2 to simultaneously enhance MnCl 2 dispersion and improve stabilization. This integrated catalyst‐absorbent system reproducibly exceeds single‐pass ammonia synthesis equilibrium. Kinetic models of the catalyst and absorbent successfully predict the experimental long‐term behavior and facilitate the design of an integrated system. These results present a framework for aligning intermittent and isolated renewable energy with ammonia synthesis by decreasing capital complexity and increasing process agility—adapting to a shifting energy landscape to continue providing fertilizers with minimum CO 2 penalty and pioneer energy storage.