https://ams.confex.com/ams/pdfpapers/71176.pdf

Fully coupled “online” chemistry within the WRF model

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 CO2 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 CO2 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.

/pdf/carbon-capture-and-storage-ccs-the-way-forward-11rgsqyer0.pdf

Carbon capture and storage (CCS): the way forward

In recent years, Carbon Capture and Storage (Sequestration) (CCS) has been proposed as a potential method to allow the continued use of fossil-fuelled power stations whilst preventing emissions of CO2 from reaching the atmosphere. Gas, coal (and biomass)-fired power stations can respond to changes in demand more readily than many other sources of electricity production, hence the importance of retaining them as an option in the energy mix. Here, we review the leading CO2 capture technologies, available in the short and long term, and their technological maturity, before discussing CO2 transport and storage. Current pilot plants and demonstrations are highlighted, as is the importance of optimising the CCS system as a whole. Other topics briefly discussed include the viability of both the capture of CO2 from the air and CO2 reutilisation as climate change mitigation strategies. Finally, we discuss the economic and legal aspects of CCS.

Carbon capture and storage update

New cements for the 21st century: The pursuit of an alternative to Portland cement

Carbon dioxide (CO2) capture using solid sorbents has been recognized as a very promising technology that has attracted intense attention from both academic and industrial fields in the last decade. It is astonishing that around 2000 papers have been published from 2011 to 2014 alone, which is less than three years after our first review paper in this journal on solid CO2 sorbents was published. In this short period, much progress has been made and the major research focus has more or less changed. Therefore, we feel that it is necessary to give a timely update on solid CO2 capture materials, although we still have to keep some important literature results published in the past years so as to keep the good continuity. We believe this work will benefit researchers working in both academic and industrial areas. In this paper, we still organize the CO2 sorbents according to their working temperatures by classifying them as such: (1) low-temperature ( 400 °C). Since the sorption capacity, kinetics, recycling stability and cost are important parameters when evaluating a sorbent, these features will be carefully considered and discussed. In addition, due to the huge amounts of cost-effective CO2 sorbents demanded and the importance of waste resources, solid CO2 sorbents prepared from waste resources and their performance are reviewed. Finally, the techno-economic assessments of various CO2 sorbents and technologies in real applications are briefly discussed.

Recent advances in solid sorbents for CO2 capture and new development trends

Fluidized bed combustion of alternative solid fuels

Mechanism and prediction of bed agglomeration during fluidized bed combustion of a biomass fuel: Effect of the reactor scale

Attrition of sorbents during fluidized bed calcination and sulphation

The agglomeration behaviour of three biomass fuels (exhausted and virgin olive husk and pine seed shells) during fluidized bed combustion in a lab-scale reactor was studied by means of SEM/EDX analysis of bed agglomerate samples. The effect of the fuel ash composition, bed temperature and sand particle size on agglomeration was investigated. The study was focused on the main fuel ash components and on their interaction with the bed sand particles. Agglomeration was favoured by high temperature, small sand size, a high fraction of K and Na and a low fraction of Ca and Mg in the fuel ash. An initial fuel ash composition close to the low-melting point eutectic composition appears to enhance agglomeration. The agglomerates examined by SEM showed a hollow structure, with an internal region enriched in K and Na where extensive melting is evident and an external one where sand particles are only attached by a limited number of fused necks. Non-molten or partially molten ash structures deposited on the sand surface and enriched in Ca and Mg were also observed. These results support an ash deposition–melting mechanism: the ash released by burning char particles inside the agglomerates is quantitatively deposited on the sand surface and then gradually embedded in the melt. The low-melting point compounds in the ash migrate towards the sand surface enriching the outermost layer, while the ash structure is progressively depleted of these compounds.

An SEM/EDX study of bed agglomerates formed during fluidized bed combustion of three biomass fuels

Batchwise fluidized-bed calcination and sulfation of a limestone were done to investigate particle comminution phenomena and their relation with parallel occurrence of reactions Operating conditions of the bed were those typical of atmospheric bubbling fluidized-bed combustors A general framework of comminution phenomena is outlined, which includes different types of fragmentations as well as attrition by abrasion Comminution processes were characterized by following the modifications of bed sorbent particle-size distribution and the elutriation rates of fines throughout conversion Mutual interactions between comminution processes and the progress of chemical reactions are assessed

Fabrizio Scala

Papers

Fluidized bed combustion of alternative solid fuels

Mechanism and prediction of bed agglomeration during fluidized bed combustion of a biomass fuel: Effect of the reactor scale

Attrition of sorbents during fluidized bed calcination and sulphation

An SEM/EDX study of bed agglomerates formed during fluidized bed combustion of three biomass fuels

Comminution of limestone during batch fluidized‐bed calcination and sulfation