Monolithic ZIF-8 and ZIF-67 adsorbents are synthesized at room temperature using a novel, ligand-assisted method. Despite reductions in crystallinity within some of the samples, monolithic zeolitic imidazolate frameworks (ZIFs) have superior volume-relative microporosity, total porosity, and surface areas relative to their particulate counterparts due to increased density. Samples synthesized using a single modulator, n-butylamine, have a hierarchical porosity resulting in improved adsorption capacities in mid-to high-sorbate pressure regions. ZIF-67 monoliths produced through mixedmodulator synthesis, n-butylamine and 1-methylimidazole, are almost entirely microporous. Vapor adsorption isotherms find that, whilst their amorphous content results in increased water uptake, monolithic ZIFs are found to possess higher surface and adsorption hydrophobicity than traditional nonpolar adsorbents. Cosorption measurements with a common VOC toluene, under humid conditions, find that these monolithic ZIF samples outperform powder equivalents, with the mixed-modulator ZIF-67 monolith capturing 28% more VOC compared to the powder ZIFs studied due to its superior volumetric efficiency. This study provides insights into the benefits of modulator-based tuning of porosity within monolithic ZIFs which, combined with their hydrophobicity, may facilitate their application for industrial organic vapor recovery or indoor air cleaning, where efficient hydrophobic adsorbents which can operate in humid environments are essential.

MIL-101(Cr)-4F(1%) proved to be a stable material under moist conditions compared to other industrial MOFs, with facile regeneration under relevant industrial conditions; plus the introduction of small amounts of water enhances the diffusion of CO2.

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Expanding populations and growing economies result in higher energy needs. Meeting this increasing demand, while lowering carbon emissions, calls for a broad energy mix and commercial deployment of solutions like carbon capture and carbon removal technologies. The scale-up of these solutions is partially hindered by the lack of materials-related information, particularly in the case of solid adsorption-based carbon capture technologies. Furthermore, experimental measurement parameters used and how data is presented lack uniformity, which makes material comparisons extremely difficult. This review examines the current state of solid sorbent characterization for carbon capture, exploring physical and chemical properties, performance parameters, and process indicators. Adsorbent performance parameters demonstrate to be the crucial link between intrinsic material properties and the overall adsorption process effectiveness and therefore are the focus of this work. This paper outlines the relevant techniques used to measure Key Performance Indicators (KPIs) related to adsorption performance such as CO2 adsorption capacity, selectivity, kinetics, ease of regeneration, stability, adsorbent cost, and environmental impact. Additionally, this study highlights the relevant experimental conditions for diluted versus concentrated CO2 streams. Lastly, efforts in harmonizing experimental data sets are considered, and an outlook on solid sorbent characterization for carbon capture processes is presented. Overall, the aim of this work is to provide the reader a critical understanding of KPIs from atomic to process scale, highlighting the importance of experimental data throughout.