• Energy Research

Abstract Energy storage is one of the most critical factors for maximising the availability of renewable energy systems while delivering firm capacity on an as- and when-required basis, thus improving the balance of grid energy. Chemical and calcium looping are two technologies, which are promising from both the point of view of minimising greenhouse gas emissions and because of their suitability for integrating with energy storage. A particularly promising route is to combine these technologies with solar heating, thus minimising the use of fossil fuels during the materials regeneration steps. For chemical looping, the development of mixed oxide carrier systems remains the highest impact research and development goal, and for calcium looping, minimising the decay in CO2 carrying capacity with natural sorbents appears to be the most economical option. In particular, sorbent stabilisers such as those based on Mg are particularly promising. In both cases, energy can be stored thermally as hot solids or chemically as unreacted materials, but there is a need to build suitable pilot plant demonstration units if the technology is to advance.

Abstract Energy storage is one of the most critical factors for maximising the availability of renewable energy systems while delivering firm capacity on an as- and when-required basis, thus improving the balance of grid energy. Chemical and calcium looping are two technologies, which are promising from both the point of view of minimising greenhouse gas emissions and because of their suitability for integrating with energy storage. A particularly promising route is to combine these technologies with solar heating, thus minimising the use of fossil fuels during the materials regeneration steps. For chemical looping, the development of mixed oxide carrier systems remains the highest impact research and development goal, and for calcium looping, minimising the decay in CO2 carrying capacity with natural sorbents appears to be the most economical option. In particular, sorbent stabilisers such as those based on Mg are particularly promising. In both cases, energy can be stored thermally as hot solids or chemically as unreacted materials, but there is a need to build suitable pilot plant demonstration units if the technology is to advance.

AbstractThis study explores the use of a dual interconnected circulating fluidized bed (CFB) for chemical looping combustion. This design can enhance gas–solid interactions, but it is difficult to control the solid transfer and circulation rates. With the use of a 1:1 scale cold‐flow model, an investigation determining the hydrodynamic behavior of the dual CFB system has been conducted. The cold‐flow system consists of two identical fast‐bed risers, each with an internal diameter of 100 mm and a height of 7 m. The simplified cold‐flow model is based on the chemical looping Pilot‐Scale Advanced CO2 Capture Technology (PACT) facility at Cranfield. Here, we have determined the minimum fluidization and transport velocities, and we have assessed the solid density profiles, transport capacity, and potential for the dilution by air/N2 leakage into the CO2 stream exiting the fuel reactor. The experimental procedure uses two different bed materials, molochite (ceramic clay) and FE100 (iron particles), and it satisfies the dynamic scaling laws to model the bed inventory within the system. The results indicate that the two fast‐bed risers share similar density and pressure profiles. Stable circulation can be achieved through pneumatic transport. The circulation rate of the system is flexible and can be adjusted by altering the fluidization velocity in the riser and by altering the bed inventory. The gas leakage from the loop seal to the cyclone was found to be sensitive to the bed height and fluidization velocity in the loop seal. However, by maintaining a loop‐seal bed height above 600 mm during operation, the outlet stream remains undiluted.

AbstractThis study explores the use of a dual interconnected circulating fluidized bed (CFB) for chemical looping combustion. This design can enhance gas–solid interactions, but it is difficult to control the solid transfer and circulation rates. With the use of a 1:1 scale cold‐flow model, an investigation determining the hydrodynamic behavior of the dual CFB system has been conducted. The cold‐flow system consists of two identical fast‐bed risers, each with an internal diameter of 100 mm and a height of 7 m. The simplified cold‐flow model is based on the chemical looping Pilot‐Scale Advanced CO2 Capture Technology (PACT) facility at Cranfield. Here, we have determined the minimum fluidization and transport velocities, and we have assessed the solid density profiles, transport capacity, and potential for the dilution by air/N2 leakage into the CO2 stream exiting the fuel reactor. The experimental procedure uses two different bed materials, molochite (ceramic clay) and FE100 (iron particles), and it satisfies the dynamic scaling laws to model the bed inventory within the system. The results indicate that the two fast‐bed risers share similar density and pressure profiles. Stable circulation can be achieved through pneumatic transport. The circulation rate of the system is flexible and can be adjusted by altering the fluidization velocity in the riser and by altering the bed inventory. The gas leakage from the loop seal to the cyclone was found to be sensitive to the bed height and fluidization velocity in the loop seal. However, by maintaining a loop‐seal bed height above 600 mm during operation, the outlet stream remains undiluted.

AbstractIn oxy‐fuel combustion, fuel is burned using oxygen together with recycled flue gas, which is needed to control the combustion temperature. This leads to higher concentrations of sulfur dioxide and sulfur trioxide in the recycled gas, which can result in the formation of sulfuric acid and enhanced corrosion. Current experimental data on SO3 formation, reaction mechanisms, and mathematical modelling have indicated significant differences in SO3 formation between air‐ and oxy‐fuel combustion for both the wet and dry flue gas recycle options. This paper provides an extensive review of sulfur trioxide formation in air‐ and oxy‐fuel combustion environments, with an emphasis on coal‐fired systems. The first part summarizes recent findings on oxy‐fuel combustion experiments, as they affect sulfur trioxide formation. In the second part, the review focuses on sulfur trioxide formation mechanisms, and the influence of catalysis on sulfur trioxide formation. Finally, the current methods for measuring sulfur trioxide concentration are also reviewed along with the major difficulties associated with those measurements using data available from both bench‐ and pilot‐scale units. © 2018 Society of Chemical Industry and John Wiley & Sons, Ltd.

AbstractIn oxy‐fuel combustion, fuel is burned using oxygen together with recycled flue gas, which is needed to control the combustion temperature. This leads to higher concentrations of sulfur dioxide and sulfur trioxide in the recycled gas, which can result in the formation of sulfuric acid and enhanced corrosion. Current experimental data on SO3 formation, reaction mechanisms, and mathematical modelling have indicated significant differences in SO3 formation between air‐ and oxy‐fuel combustion for both the wet and dry flue gas recycle options. This paper provides an extensive review of sulfur trioxide formation in air‐ and oxy‐fuel combustion environments, with an emphasis on coal‐fired systems. The first part summarizes recent findings on oxy‐fuel combustion experiments, as they affect sulfur trioxide formation. In the second part, the review focuses on sulfur trioxide formation mechanisms, and the influence of catalysis on sulfur trioxide formation. Finally, the current methods for measuring sulfur trioxide concentration are also reviewed along with the major difficulties associated with those measurements using data available from both bench‐ and pilot‐scale units. © 2018 Society of Chemical Industry and John Wiley & Sons, Ltd.

7 pages, 2 figures, 9 tables.-- Printed version published Mar 21, 2007. Flue gas CO2 capture using a Ca-based chemical looping system has been shown to be potentially more cost-effective than traditional amine-based systems in bench-scale testing. The results of these initial tests are projected, using an Excel-based economic model, to estimate the 30-year levelized cost of CO2 capture per metric ton (t) for a utility-scale power plant. An order of magnitude capital and operating estimate for a 360 MW pressurized fluidized bed combustor (PFBC) is presented, assuming a western Canadian location. Additional costs for calciners, O2 plant, and related equipment necessary to create a Ca-based CO2 chemical capture loop are presented separately. These costs are evaluated in a series of spreadsheets, and the impact of process flows, as well as capital, operating/maintenance, and feedstock costs are determined in a sensitivity analysis. The financial results for CO2 capture are found to compare favorably with amine-based capture systems. Peer reviewed