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.

The promise of ultrapermeable polymers, such as poly(trimethylsilylpropyne) (PTMSP), for reducing the size and increasing the efficiency of membranes for gas separations remains unfulfilled due to their poor selectivity. We report an ultrapermeable polymer of intrinsic microporosity (PIM-TMN-Trip) that is substantially more selective than PTMSP. From molecular simulations and experimental measurement we find that the inefficient packing of the two-dimensional (2D) chains of PIM-TMN-Trip generates a high concentration of both small (<0.7 nm) and large (0.7-1.0 nm) micropores, the former enhancing selectivity and the latter permeability. Gas permeability data for PIM-TMN-Trip surpass the 2008 Robeson upper bounds for O2/N2, H2/N2, CO2/N2, H2/CH4 and CO2/CH4, with the potential for biogas purification and carbon capture demonstrated for relevant gas mixtures. Comparisons between PIM-TMN-Trip and structurally similar polymers with three-dimensional (3D) contorted chains confirm that its additional intrinsic microporosity is generated from the awkward packing of its 2D polymer chains in a 3D amorphous solid. This strategy of shape-directed packing of chains of microporous polymers may be applied to other rigid polymers for gas separations.

A novel polymer of intrinsic microporosity (PIM) was prepared from a diaminobenzotriptycene monomer using a polymerization reaction based on Tröger’s base formation. The polymer (PIM-BTrip-TB) demonstrated an apparent Brunauer, Emmet, and Teller (BET) surface area of 870 m² g^–1, good solubility in chloroform, excellent molecular mass, high inherent viscosity and provided robust thin films for gas permeability measurements. The polymer is highly permeable (e.g., PH₂ = 9980; PO₂ = 3290 Barrer) with moderate selectivity (e.g., PH₂/PN₂ = 11.0; PO₂/PN₂ = 3.6) so that its data lie over the 2008 Robeson upper bounds for the H₂/N₂, O₂/N₂, and H₂/CH₄ gas pairs and on the upper bound for CO₂/CH₄. On aging, the polymer demonstrates a drop in permeability, which is typical for ultrapermeable polymers, but with a significant increase in gas selectivities (e.g., PO₂ = 1170 Barrer; PO₂/PN₂ = 5.4).

The impurities present in carbon dioxide (CO2) streams for Carbon Capture and Storage (CCS) schemes are extremely important for CO2 pipeline and ship transportation affecting, for instance, the range of operation, safety considerations, fracture, cracking, corrosion control, dispersion in the event of a release, fluid density, operating pressure and temperature and the quantity of CO2 that can be transported. The range and levels of potential impurities present in captured CO2 from CO2 capture facilities will differ between sources and also between the capture technologies installed at the CO2 emission sources. However, the potential CO2 specifications that could enter the transport and storage systems, particularly from industrial sources, remain relatively under-researched. Consequently, the effect of these potential impurities in CO2 streams on CO2 transportation also needs to be understood. This paper summarises the main findings of an IEAGHG study, “Impact of CO2 Impurity on CO2 Compression, Liquefaction and Transportation”, commissioned to identify potential impurities and address the consequences of their impact on CO2 transportation

Gas transport properties of PIM-EA(H₂)-TB, a microporous Tröger’s base polymer, were systematically studied over a range of pressure and temperature. Permeability coefficients of pure CO₂, N₂, CH₄ and H₂ were determined for upstream pressures up to 20 bar and temperatures up to 200 °C. PIM-EA(H₂)-TB exhibited high permeability coefficients in absence of plasticization phenomena. The permeability coefficient of N₂, CH₄ and H₂ increased with increasing temperature while CO₂ permeability decreased with increasing temperature as expected for a glassy polymer. The diffusion and solubility coefficients were also analysed individually and compared with other polymers of intrinsic microporosity. From these results, the activation energies of permeation, diffusion and sorption enthalpies were calculated using an Arrhenius equation.