This dissertation investigates the pressing issue of climate change, identifying carbon dioxide as its main driver and introduces Direct Air Capture (DAC) as a crucial technology for achieving significant reductions in net global emissions. Through an extensive review of existing literature on DAC, it examines various methods and materials developed for this purpose, highlighting the ongoing efforts, advancements, and potential for real-world application. A novel sorbent, quaternary ammonium-functionalized poly(arylene ether sulfone) is explored for DAC via the moisture swing process. This sorbent exhibited the ability to capture and release atmospheric CO2 by a swing in moisture. Effects of form factors of powder, free standing dense membrane and thin film composite membrane were also evaluated for DAC. Furthermore, the dissertation explores modifications to poly(arylene ether sulfones) – polymers primarily used in desalination processes – to enhance water scarcity solutions by improving desalination membrane hydrophilicity and reducing fouling. This enhancement is achieved through the incorporation of zwitterionic groups into the polymer structure. Additionally, it investigates the synthesis of polysulfone polymers from lignin-derivable monomers, offering a greener alternative to traditional polysulfones used in desalination due to their environmental and health concerns. Polysulfones derivable from lignin exhibited comparable thermal properties and enhanced hydrophilicity compared to petroleum-derived polymers, showing considerable promise. Lastly, this dissertation investigates a potential hybrid system for desalination and direct ocean capture by integrating redox-active compounds into desalination membranes. This aims to achieve a pH swing that facilitates the formation of dissolved CO2.

CO2 capture from ambient air (often referred to as direct air capture or DAC) is one of the Carbon Dioxide Removal methodologies that may limit Global Warming. High energy demand and high cost are currently serious barriers for large-scale DAC deployments. Moisture-controlled CO2 sorption is a novel technology for DAC, where CO2 sorption cycles are driven solely by changes in surrounding humidity. In contrast to traditional temperature-swing adsorption cycles, water is a cheaper source of exergy than high-grade heat or electricity and moisture-controlled CO2 sorption may reduce the cost of DAC. However, analytic models that describe this sorption system have not been well established, especially in a quantitative manner. In this dissertation the author first establishes both static and kinetic models analytically with bottom-up approaches from the governing equations. These models are of scientific interest and also of industrial importance. They were validated by literature data and custom experiments. In a second part of the dissertation, the author explores the application of moisture-controlled materials in the form of membranes that actively pump CO2 against a concentration gradient. These explorations are guided by the quantitative models developed in the first part of the dissertation. In CO2 separation technologies relying on actively pumping membranes, a moisture-controlled CO2 sorbent is used as either a gas-gas membrane contactor or a gas-liquid membrane contactor. The author experimentally and theoretically determined that a specific commercial anion exchange membrane that was considered a plausible candidate does not satisfy the requirements for such an active membrane as a consequence of its slow kinetics of carbon transport. Requirements for materials to serve as active membranes have been clarified, which is of great interest for industrial application and will provide a starting point for future material design and development.