Magnesium oxide/cesium carbonate composites as well as a cadmium oxide/sodium halide mixture have been previously described as potential candidates for pre-combustion carbon dioxide capture. Here, the effects of water and hydrogen alongside carbon dioxide were examined in simulated partial pressure swing experiments analyzed by thermogravimetric means. It was shown that the magnesium/cesium sorbents are tolerant to hydrogen at a temperature of 370 °C and that their working capacities over 25 cycles are enhanced by the addition of water to the sorption gas stream. The cadmium/sodium iodide sorbent showed a stable working capacity for 23 sorption cycles at 285 °C, but tended to lose working capacity afterwards. At a temperature of 305 °C, a significant loss in capacity was observed during sorption cycling. As reduction in an inert gas/hydrogen mixture was not found to commence below 400 °C, a halide promoter disintegration mechanism is assumed to be the cause of the decay.The sorption of H 2 S was also examined. Both cadmium and magnesium-based materials showed a significant uptake of H 2 S, which was hard to desorb. It appears that H 2 S sorption competes alongside carbon dioxide sorption causing a reduction in working capacities over multiple cycles. Powder X-ray diffraction showed that the cadmium-based sorbent forms CdS upon H 2 S sorption, whereas the MgO phase of the magnesium-based sorbent is not changed. A new cesium phase was formed from cesium carbonate with H 2 S, which is probably a previously unreported magnesium-cesium sulphide mixed phase.