Efficient CO transformation from a waste product to a carbon source for chemicals and fuels will require reaction conditions that effect its reduction. We developed a "super-dry" CH reforming reaction for enhanced CO production from CH and CO We used Ni/MgAlO as a CH-reforming catalyst, FeO/MgAlO as a solid oxygen carrier, and CaO/AlO as a CO sorbent. The isothermal coupling of these three different processes resulted in higher CO production as compared with that of conventional dry reforming, by avoiding back reactions with water. The reduction of iron oxide was intensified through CH conversion to syngas over Ni and CO extraction and storage as CaCO CO is then used for iron reoxidation and CO production, exploiting equilibrium shifts effected with inert gas sweeping (Le Chatelier's principle). Super-dry reforming uses up to three CO molecules per CH and offers a high CO space-time yield of 7.5 millimole CO per second per kilogram of iron at 1023 kelvin.
A detailed study of new oxygen carrier materials, Mg–Fe–Al–O, with various loadings of iron oxide (10–100 wt% Fe2O3) is carried out in order to investigate the relationship between material transformation, stability and CO yield from CO2conversion.
Coupling decentralized biomethane generation to centralized CO production via gas grid redistribution can be an economically viable CO2 utilization strategy.
Driven by the need to develop technologies for converting CO 2 , an extraordinary array of chemical looping based process concepts has been proposed and researched over the past 15 years. This review aims at providing first a historical context of the molecule CO 2 , which sits at the center of these developments. Then, different types of chemical looping related to CO 2 are addressed, with attention to process concepts, looping materials, and reactor configurations. Herein, focus lies on the direct conversion of carbon dioxide into carbon monoxide, a process deemed to have economic potential.
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