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Air purification of ammonia, a toxic industrial chemicals (TICs), by adsorption process on Metal-Organic Framework solids is attracting high scientific and commercial interests. While active carbon based adsorbents required high level of relative humidity for achieving proper performance ammonia capture, zeolite performance degrades in presence of humidity. For MOFs, the presence of humidity has been shown to be MOF dependent, either beneficial or detrimental. It appears that the role of humidity is of key importance and that different ammonia adsorption mechanisms co-exist depending on the material's physico-chemical features. Based on a screening of various microporous adsorbents including carbons, zeolites and MOFs, we show that in the presence of humidity, the ammonia uptake mostly follows the Henry law of ammonia solubilization in water. At the exception of Copper based MOF, the ammonia capture is mostly correlated with the amount of “condensed water” in the micropore. We also generally observe a systematic higher uptake than the Henry law which can be attributed to the effect of confinement i. e surface-condensed phase interaction. [ABSTRACT FROM AUTHOR]

Microporous cavities and channels of zeolites frameworks have been used for decades for the encapsulation of cations, complexes and metals. In the particular case of metals, nanoparticles are usually formed after post-synthesis modifications such as ion-exchange or wetness impregnation. Tough encapsulation can provide a strict control of the nanoparticle size as well as a limitation of aggregation at high temperature; encapsulated nanoparticles are often hardly accessible due to diffusion limitations of reactants in sub-nanometric micropores. Recent developments in zeolite synthesis have offered a new class of materials with hierarchical structures or unusual morphologies in which the mean diffusion path is considerably reduced. Those zeolites with inter-crystalline and/or intra-crystalline mesopore systems are particularly adapted for supporting nanoparticles both in microporous cavities of the framework and in mesoporous channels. More sophisticated architectures such as yolk/core–shell materials, in which nanoparticles are protected against poisoning or sintering by a thin zeolite shell, are particularly attractive. In contrast to nanometric intrinsic cavities of zeolite frameworks, a large internal void is available for chemical reactions and such catalysts can be considered as nanoreactors in which the reaction is essentially governed by the permeability of the shell. This review focuses on the most recent progress as well as perspectives in the design of zeolite-containing metal nanoparticles, which differ from traditional materials by the originality of the synthesis method or the morphology of the support. [ABSTRACT FROM AUTHOR]

We report herein the upscaled synthesis and shaping of UiO66-COOH for NH3 air purification. The synthesis of the zirconium-based MOF was carried out in a batch reactor in an aqueous suspension with a yield of 89% and a space-time yield of 350 kg/day/m3. Neither toxic chemicals nor organic solvents were used, allowing this MOF to be employed in individual or collective air purification devices. Freeze-granulation and extrusion shaping techniques were investigated. The NH3 air purification performances of UiO66-COOH in bead, tablet and extrudate forms were compared to those of commercial carbon based materials (type K adsorbents from3M and Norit). Testing conditions were chosen to reflect current standards for ammonia concentration (600-1200 ppm) and velocity. In addition, the breakthrough measurements were carried out at three different relative humidity levels (0%, 40%, and 70%). Pellets and extrudates of UiO66-COOH outperformed commercial benchmark adsorbents in all conditions, especially in dry conditions, for which the commercial adsorbents suffered impaired ammonia uptake and shortened service life. Extrudates of UiO66-COOH also withstood attrition after intensive shaking. [ABSTRACT FROM AUTHOR]

Hollow capsules with dimensions below 1 μm have recently attracted much attention due to their potential applications as catalysts as well as biomedical and pharmaceutical vectors for controlled drug delivery. Among them, hollow zeolites are particularly interesting because they possess (i) a crystalline structure, which greatly improves their hydrothermal and chemical stability as compared to amorphous silica analogs and (ii) a microporous network that acts as a shape-selective membrane. Moreover, their properties can be continuously tuned by changing their composition, in particular the framework aluminum content. In this perspective review, we examine the recent progress in the development of synthetic methods for the preparation of hollow zeolite and zeotype structures, from templating routes providing large polycrystalline capsules to controlled dissolution methods leading to nanometer-sized hollow single crystals. The applications of these materials will be illustrated and discussed, namely their main potential as catalytic nanoreactors, these being materials particularly adapted for the encapsulation and the confinement of metal nanoparticles. Critical perspectives on future materials with specific properties are also addressed, particularly those with less common zeolite structures and/or compositions. [ABSTRACT FROM AUTHOR]

Review: 105 refs. [ABSTRACT FROM AUTHOR]