Chemical looping combustion

Chemical looping combustion (CLC) is a technological process typically employing a dual fluidized bed system. CLC operated with an interconnected moving bed with a fluidized bed system, has also been employed as a technology process. In CLC, a metal oxide is employed as a bed material providing the oxygen for combustion in the fuel reactor. The reduced metal is then transferred to the second bed (air reactor) and re-oxidized before being reintroduced back to the fuel reactor completing the loop. Fig 1 shows a simplified diagram of the CLC process. Fig 2 shows an example of a dual fluidized bed circulating reactor system and a moving bed-fluidized bed circulating reactor system.

Isolation of the fuel from air simplifies the number of chemical reactions in combustion. Employing oxygen without nitrogen and the trace gases found in air eliminates the primary source for the formation of nitrogen oxide (NO_x), produces a flue gas composed primarily of carbon dioxide and water vapor; other trace pollutants depend on the fuel selected.

Chemical looping combustion (CLC) uses two or more reactions to perform the oxidation of hydrocarbon-based fuels. In its simplest form, an oxygen-carrying species (normally a metal) is first oxidized in the air forming an oxide. This oxide is then reduced using a hydrocarbon as a reducer in a second reaction. As an example, an iron based system burning pure carbon would involve the two redox reactions:

If (1) and (2) are added together, the reaction set reduces to straight carbon oxidation i.e.:

CLC was first studied as a way to produce CO₂ from fossil fuels, using two interconnected fluidized beds.^[3] Later it was proposed as a system for increasing power station efficiency.^[4] The gain in efficiency is possible due to the enhanced reversibility of the two redox reactions; in traditional single stage combustion, the release of a fuel's energy occurs in a highly irreversible manner - departing considerably from equilibrium. In CLC, if an appropriate oxygen carrier is chosen, both redox reactions can be made to occur almost reversibly and at relatively low temperatures. Theoretically, this allows a power station using CLC to approach the ideal work output for an internal combustion engine without exposing components to excessive working temperatures.

Fig 3 illustrates the energy exchanges in a CLC system graphically and shows a Sankey diagram of the energy fluxes occurring in a reversible CLC based engine. Studying Fig 1, a heat engine is arranged to receive heat at high temperatures from the exothermic oxidation reaction. After converting part of this energy to work, the heat engine rejects the remaining energy as heat. Almost all of this heat rejection can be absorbed by the endothermic reduction reaction occurring in the reducer. This arrangement requires the redox reactions to be exothermic and endothermic respectively, but this is normally the case for most metals.^[5] Some additional heat exchange with the environment is required to satisfy the second law; theoretically, for a reversible process, the heat exchange is related to the standard state entropy change, ΔS^o, of the primary hydrocarbon oxidation reaction as follows:

Q_o = T_oΔS^o

However, for most hydrocarbons, ΔS^o is a small value and, as a result, an engine of high overall efficiency is theoretically possible.^[6]

Although proposed as a means of increasing efficiency, in recent years, interest has been shown in CLC as a carbon capture technique.^[7][8] Carbon capture is facilitated by CLC because the two redox reactions generate two intrinsically separated flue gas streams: a stream from the air reactor, consisting of atmospheric N
₂ and residual O
₂, but sensibly free of CO₂; and a stream from the fuel reactor predominately containing CO₂ and H
₂O with very little diluent nitrogen. The air reactor flue gas can be discharged to the atmosphere causing minimal CO₂ pollution. The reducer exit gas contains almost all of the CO₂ generated by the system and CLC therefore can be said to exhibit 'inherent carbon capture', as water vapor can easily be removed from the second flue gas via condensation, leading to a stream of almost pure CO₂. This gives CLC clear benefits when compared with competing carbon capture technologies, as the latter generally involve a significant energy penalty associated with either post combustion scrubbing systems or the work input required for air separation plants. This has led to CLC being proposed as an energy efficient carbon capture technology,^[9][10] able to capture nearly all of the CO₂, for example, from a Coal Direct Chemical Looping (CDCL) plant.^[11][12] A continuous 200-hour demonstration results of a 25 kW_th CDCL sub-pilot unit indicated nearly 100% coal conversion to CO₂ with no carbon carryover to the air reactor.^[13][14]

First operation of chemical-looping combustion with gaseous fuels was demonstrated in 2003,^[15] and later with solid fuels in 2006.^[16] Total operational experience in 34 pilots of 0.3 to 3 MW is more than 9000 h.^[17][18][19] Oxygen carrier materials used in operation include monometallic oxides of nickel, copper, manganese and iron, as well as various combined oxides including manganese oxides.combined with calcium, iron and silica. Also natural ores have been in use, especially for solid fuels, including iron ores, manganese ores and ilmenite.

A detailed technology assessment of chemical-looping combustion of solid fuel, i.e. coal, for a 1000 MW_th power plant shows that the added CLC reactor costs as compared to a normal circulating fluidized bed boiler are small, because of the similarities of the technologies. Major costs are instead CO₂ compression, needed in all CO₂ capture technologies, and oxygen production. Molecular oxygen production may also be needed in certain CLC configuration for polishing the product gas from the fuel reactor. In all the added costs were estimated to 20 €/tonne of CO₂ whereas the energy penalty was 4%.^[20]

A variant of CLC is Chemical-Looping Combustion with Oxygen Uncoupling (CLOU) where an oxygen carrier is used that releases gas-phase oxygen in the fuel reactor, e.g. CuO/Cu
₂O.^[21] This is helpful for achieving high gas conversion, and especially when using solid fuels, where slow steam gasification of char can be avoided. CLOU operation with solid fuels shows high performance^[22][23]

Chemical Looping can also be used to produce hydrogen in Chemical-Looping Reforming (CLR) processes.^[24][25] In one configuration of the CLR process, hydrogen is produced from coal and/or natural gas using a moving bed fuel reactor integrated with a steam reactor and a fluidized bed air reactor. This configuration of CLR can produce greater than 99% purity H₂ without the need for CO₂ separation.^[19][26]

Comprehensive overviews of the field are given in recent reviews on chemical looping technologies.^[7][27][28]

In summary, CLC can achieve both an increase in power station efficiency simultaneously with low energy penalty carbon capture. Challenges with CLC include the operation of dual fluidized bed (maintaining carrier fluidization while avoiding crushing and attrition^[29]), and maintaining carrier stability over many cycles.

• Chemical looping reforming and gasification
• Combustion
• Oxy-fuel combustion
• Oxidizing agent
• Redox (reduction/oxidation reaction)
• Carbon capture and storage
• Lane hydrogen producer

• "CO2 Capture – homepage". entek.chalmers.se.
• chemical-looping.at
• "Chemical Looping". Institute for Combustion Science, Western Kentucky University. Archived from the original on 2012-10-22.
• "Research activities". Instituto de Carboquímica. Archived from the original on Mar 3, 2016.
• "Imperial College Centre for Carbon Capture and Storage (IC4S)". Carbon Capture and Storage, Imperial College London. Archived from the original on Mar 3, 2016.
• "SP4: Chemical Looping Combustion". ENCAP. Archived from the original on 2008-04-21.
• "Carbon capture and chemical looping technology - an update on progress". Webinar recording, Carl Bozzuto and the Global CCS Institute, 11 July 2012.