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      Chemical looping beyond combustion – a perspective

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          Abstract

          Facilitated by redox catalysts capable of catalytic reactions and reactive separation, chemical looping offers exciting opportunities for intensified chemical production.

          Abstract

          As a promising approach for carbon dioxide capture, chemical looping combustion has been extensively investigated for more than two decades. However, the chemical looping strategy can be and has been extended well beyond carbon capture. In fact, significant impacts on emission reduction, energy conservation, and value-creation can be anticipated from chemical looping beyond combustion (CLBC). This article aims to demonstrate the versatility and transformational benefits of CLBC. Specifically, we focus on the use of oxygen carriers or redox catalysts for chemical production – a $4 trillion industry that consumes 40.9 quadrillion BTU of energy. Compared to state-of-the-art chemical production technologies, we illustrate that chemical looping offers significant opportunities for process intensification and exergy loss minimization. In many cases, an order of magnitude reduction in energy consumption and CO 2 emission can be realized without the needs for carbon dioxide capture. In addition to providing various CLBC examples, this article elaborates on generalized design principles for CLBC, potential benefits and pitfalls, as well as redox catalyst selection, design, optimization, and redox reaction mechanism.

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          Carbon capture and storage (CCS): the way forward

          Carbon capture and storage (CCS) is vital to climate change mitigation, and has application across the economy, in addition to facilitating atmospheric carbon dioxide removal resulting in emissions offsets and net negative emissions. This contribution reviews the state-of-the-art and identifies key challenges which must be overcome in order to pave the way for its large-scale deployment. Carbon capture and storage (CCS) is broadly recognised as having the potential to play a key role in meeting climate change targets, delivering low carbon heat and power, decarbonising industry and, more recently, its ability to facilitate the net removal of CO 2 from the atmosphere. However, despite this broad consensus and its technical maturity, CCS has not yet been deployed on a scale commensurate with the ambitions articulated a decade ago. Thus, in this paper we review the current state-of-the-art of CO 2 capture, transport, utilisation and storage from a multi-scale perspective, moving from the global to molecular scales. In light of the COP21 commitments to limit warming to less than 2 °C, we extend the remit of this study to include the key negative emissions technologies (NETs) of bioenergy with CCS (BECCS), and direct air capture (DAC). Cognisant of the non-technical barriers to deploying CCS, we reflect on recent experience from the UK's CCS commercialisation programme and consider the commercial and political barriers to the large-scale deployment of CCS. In all areas, we focus on identifying and clearly articulating the key research challenges that could usefully be addressed in the coming decade.
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            Beyond fossil fuel–driven nitrogen transformations

            Nitrogen is fundamental to all of life and to many industrial processes. Nitrogen in its various oxidation states comprises the global nitrogen cycle, with the change between forms being redox reactions involving electrons and protons. The interchange of nitrogen oxidation states constitutes some of the most important industrial processes, with the energy for these processes being provided largely by fossil fuel. A key goal of research in the field of nitrogen chemistry is to minimize the use of fossil fuels by developing more efficient heterogeneous, homogeneous, or biological catalysts, or by inventing new energy-efficient processes that rely on catalysts. These approaches, as well as the challenges involved, are discussed in this review. This review article reports on the current state of the field of nitrogen activation chemistry and discusses future directions.
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              Catalytic dehydrogenation of light alkanes on metals and metal oxides.

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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
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                Journal
                EESNBY
                Energy & Environmental Science
                Energy Environ. Sci.
                Royal Society of Chemistry (RSC)
                1754-5692
                1754-5706
                March 18 2020
                2020
                : 13
                : 3
                : 772-804
                Affiliations
                [1 ]Department of Chemical and Biomolecular Engineering
                [2 ]North Carolina State University
                [3 ]Raleigh
                [4 ]USA
                [5 ]State Key Laboratory of Complex Nonferrous Metal Resources Clean Utilization
                [6 ]Department of Mechanical and Process Engineering
                [7 ]Laboratory of Energy Science and Engineering
                [8 ]ETH Zurich
                [9 ]Zurich
                [10 ]Switzerland
                Article
                10.1039/C9EE03793D
                d3187add-b343-478b-ad62-793a477f0c5e
                © 2020

                http://creativecommons.org/licenses/by-nc/3.0/

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