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Exceeding Single-Pass Equilibrium with Integrated Absorption Separation for Ammonia Synthesis Using Renewable Energy-Redefining the Haber-Bosch Loop

机译:超越单通平平衡,使用可再生能源 - 重新定义Haber-Bosch Loop的氨合成的集成吸收分离

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摘要

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 CeO2 support and Cs electronic promotion to remove hydrogen and ammonia inhibition, respectively, creating a catalyst with low-temperature (300 degrees C) activity that quickly approaches equilibrium. The absorbent uses MnCl2 to avoid the acid releasing decomposition of conventional absorbents like MgCl2, and a support of SiO2 to simultaneously enhance MnCl2 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 CO2 penalty and pioneer energy storage.
机译:通过Haber-Bosch工艺的氨的合成已经在化学工业的基础上超过100年,但是当能量和原料源从化石燃料切换到可再生电时,该过程需要重新实现。在此,在较较少的过程中,对绿氨技术的基础进行了再循环过程中,证明了氨合成和分离的成功整合。基于钌的催化剂使用纳米结构CeO2支持和CS电子促进,以分别去除氢和氨抑制,产生具有迅速接近平衡的低温(<300℃)活性的催化剂。吸收剂使用MnCl2以避免诸如MgCl 2的常规吸收剂的酸释放分解,以及SiO 2的载体同时增强MnCl 2分散并改善稳定化。该集成催化剂 - 吸收体系可再现超过单通过氨合成平衡。催化剂和吸收剂的动力学模型成功预测了实验性的长期行为,并促进了集成系统的设计。这些结果在通过降低资本复杂性和增加流动性能景观以继续提供具有最小二氧化碳罚款和先驱能量储存的氨基综合,以使氨合成对准和分离可再生能量与氨合成对齐和分离可再生能量。

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